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  • 1
    Electronic Resource
    Electronic Resource
    Modelling the constancy of X (1994)
    Springer
    Astrophysics and space science 216 (1994), S. 153-154 
    Details
    ISSN: 1572-946X
    Keywords: Chemistry ; Molecular Hydrogen ; Cloud Models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Observations of the CO J=1-0 line are commonly used as a tracer for molecular material in clouds. The ratio of the H2 column density to the integrated intensity of this line,X, is often taken to be constant, despite theoretical and observational uncertainty. We have tried to identify how this ratio depends on cloud parameters, testing a simple theoretical argument suggesting its invariance with respect to density. The apparent constancy can be understood if clouds are clumpy on scales of Av ≈ 1-2 mag.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00982486
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  • 2
    Electronic Resource
    Electronic Resource
    Image formation of alkyl-pendent aromatic polyimide by photocoupling with aromatic ketones (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 57-65 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Positive und negative Photostrukturen wurden in einem Polyimid (PI) aus 4,4′-Biphthalsäureanhydrid (BPA) und 4,4′-Diamino-3,3′-dimethyldiphenylmethan (DADMDPM), PI(BPA/DADMDPM) erzeugt, nachdem dieses mit Michlers Keton (MK) bzw. Benzophenon (BP) dotiert und einer ultravioletten Strahlung von 400 ± 50 nm ausgesetzt und naß entwickelt wurde. Das Prinzip der positiven Abbildung basiert auf dem Photokupplungseffekt von MK mit PI, der die Löslichkeit des Polyimids erhöht und so die Entwicklung eines Positivmusters ermöglicht. Die Erzeugung negativer Muster wird durch intermakromolekulare Wasserstoffbrücken zwischen der Carbonylgruppe des Imid-Rings und der Hydroxygruppe, die bei der photoinduzierten Kupplung von Benzophenon mit dem Polyimid gebildet wird, bewirkt. Die lithographische Auswertung zeigt, daß der mit MK dotierte, positive Polyimidfilm nicht in der Lage ist, brauchbare Muster zu erzeugen, da die UV-Wellenlängen von MK absorbiert werden, wodurch die Photokupplung in den tieferen Schichten des Films verhindert wird. Andererseits können in dem 0,6 μm dicken, mit Benzophenon dotierten Polyimidfilm sogar 2 μm schmale Linien aufgelöst werden.
    Notes: Positive and negative photostructures are formed after the polyimide (PI) of 4,4′-biphthalic anhydride (BPA) and 4,4′-diamino-3,3′-dimethyldiphenylmethane (DADMDPM), PI(BPA/DADMDPM) is doped with Michler′s ketone (MK) and benzophenone (BP), respectively, and is subjected to UV light (400 ± 50 nm) irradiation and solvent development. The principle of positive feature formation is based on the photocoupling of MK with PI, which increases PI solubility and thus enables a positive pattern to be developed. The phenomenon of negative photopatterning results from intermacromolecular H-bonding between the carbonyl group of the imide ring and the hydroxy group which is formed in the photoinduced coupling reaction between BP and PI. Lithographic evaluation shows that the MK-doped positive-acting PI film cannot form useful patterns because UV wavelengths are strongly absorbed by MK, which limits the depth of photocoupling in the film. On the other hand, 2-μm-wide lines can be resolved in the BP-doped negative-acting 0.6-μm-thick PI film.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052140106
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  • 3
    Electronic Resource
    Electronic Resource
    Blends of polyamide 6 and poly(etheraroylhydrazide)s prepared concurrently with polyhydrazide polymerization (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 101-113 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyhydrazid/Polyamid-Blends (PEHZ12/PA6) wurden durch Niedrigtemperatur-Polykondensation von 4,4′-Dichlorformyl-α,ω-diphenoxydodecan und Terephthaloyldihydrazid (TDH) zu Poly(etheraroylhydrazid) in Gegenwart von Polyamid 6 synthetisiert. Die DSC-Analysen lassen vermuten, daß die zwei Polymerkomponenten nicht wechselwirken. Bei der Extraktion des PA6-Anteils der Blends mit Ameisensäure zeigt die Charakterisierung des PEHZ12-Extraktionsrückstands aber, daß zumindest bei bestimmten Zusammensetzungen Wechselwirkungen zwischen den Komponenten auftreten. Modellreaktionen erlauben die Annahme, daß die PEHZ12-Polymerisation zwischen den Amino-Endgruppen des PA6 und den wachsenden PEHZ12-Polymerketten abläuft.
    Notes: Poly(etheraroylhydrazide) is synthesized in the presence of PA6 by means of low-temperature condensation polymerization of 4,4′-dichloroformyl-α,ω-diphenoxydodecane with terephthaloyl dihydrazide (TDH) in order to prepare polyhydrazide/poly-amide 6 (PEHZ12/PA6) blends. The thermal analysis of the blends by DSC seems to indicate that the two polymers are not interacting. Nevertheless, when the blends are subjected to an extraction process with formic acid in order to remove the PA6, the characterization of the residual PEHZ12 reveales that some interactions do occur between the constituent polymers, at least for selected compositions. Model experiments permit to hypothesize that the polymerization of PEHZ12 proceeds with a chemical interaction between amino end groups of PA6 and growing PEHZ12 chains.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052140110
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  • 4
    Electronic Resource
    Electronic Resource
    Die kristallisation von polybutylenterephthalat (PBT) und polycarbonat (PC) im polymerblend PBT/PC (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 179-196 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The crystallization behavior of PBT as well as PC is changed in the controlled-processed blend due to intermolecular interactions between the different macromolecules in molten state.If the kinetics of the crystallization process prevents a crystallization-induced separation, the partial miscibility of the amorphous phases, measured by the glass transition temperatures, will lead to a decrease of the crystallinity of PBT. The crystallinity, normalized to the concentration of PBT in the blend, is independent from the concentration of PC at low coolling rates.At high cooling rates, PBT is crystallizing stepwise in the blend PBT/PC 40/60 wt.-%. The crystallization temperature in the anisothermic crystallization process is increased at low contents of PC due to a changed nucleation mechanism. The half-time of crystallization is increasing in blends with an increasing PC-content in isothermic crystallization experiments.The normally amorphous PC crystallizes considerably fast in presence of PBT in PC-rich blends. The crystallization or change in the state of order of PC was measured in situ by X-ray diffraction. Calorimetric experiments confirm this result and allow a quantitative estimation of the PC-crystallinity, which amounts to some 20% in the blend PBT/PC 5/95 wt.-%.
    Notes: Das Kristallisationsverhalten sowohl von PBT als auch von PC ist im definiert verarbeiteten Blend infolge intermolekularer Wechselwirkungen zwischen den unterschiedlichen Molekülen in der Schmelze verändert.Die über die Glasübergangstemperaturen gemessene teilweise Mischbarkeit der amorphen Phasen führt bei PBT zu einer Erniedrigung des Kristallinitätsgrades, wenn die kinetischen Bedingungen des Kristallisationsprozesses keine kristallisationsbedingte Entmischung zulassen. Der auf den PBT-Anteil normierte Kristallinitätsgrad ist bei kleinen Abkühlgeschwindigkeiten vom PC-Anteil unabhängüg.In der Mischung PBT/PC 40/60 Gew.-% kommt es bei hohen Kühlraten zu einer fraktionierten Kristallisation. Die Kristallisationstemperatur bei anisothermer Kristallisation ist bei geringen PC-Gehalten durch Änderung des Keimbildungsmechanismus erhöht. Bei isothermer Kristallisation steigt mit zunehmendem PC-Anteil die Kristallisationshalbwertszeit des PBT an.Das normalerweise amorphe PC kann in Gegenwart von PBT in den PC-reichen Mischungen besonders schnell kristallisieren, wobei der Kristallisations- bzw. Ordnungsprozeß des PC in situ mittels der Röntgenbeugung gemessen wurde. Kalorimetrische Untersuchungen bestätigen dieses Ergebnis und erlauben eine quantitative Abschätzung des PC-Kristallinitätsgrades zu ca. 20% im Blend PBT/PC 5/95 Gew.-%.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052140116
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  • 5
    Electronic Resource
    Electronic Resource
    Photoreactions in halogen-containing negative-tone novolac resists (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 197-210 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Elementaranalytische sowie NMR-, IR- und UV-spektroskopische Untersuchungen zeigen, daß die Photolyse von Halogenphenolnovolaken zur Substitution der Halogenatome durch Wasserstoff, der Bildung chinoider Gruppen und intermolekularen Vernetzung führt. Die Geschwindigkeit der Halogeneliminierung hängt von der Art des Halogens ab. Sie steigt in der Reihenfolge F 〈 Cl 〈 Br 〈 I. Die Chloreliminierung aus der 4-Position ist gegenüber der aus der 2- und 3-Position begünstigt. Außerdem verläuft die Abspaltung para-ständiger Chloratome aus Dimeren schneller als aus Trioder Tetrameren. ESR-Messungen bei 77 K sowie die Laserblitzphotolyse bei 296 K deuten auf die intermediäre Bildung von Phenoxyl- und Arylradikalen. Lithographische Tests belegen die hohe UV-Empfindlichkeit von Resisten auf der Basis von Halogenphenolnovolaken. Im Vergleich zu nichthalogenhaltigen Novolakresisten wird eine 6 - 10fache (System: 4-Chlorphenolnovolak/4,4′-Bisazidobiphenyl (5%)) bzw. eine ca. 25fache (System: 4-Chlorphenol-/m-Cresolnovolak/Hexamethoxymethylmelamin (5%)) Steigerung der Empfindlichkeit erreicht. Zur Interpretation wird ein Mechanismus postuliert, demzufolge die durch Halogenabspaltung hervorgerufene Sekundärradikalbildung zu einer zusätzlichen Vernetzung beiträgt. In den melaminhaltigen Resisten katalysiert der gebildete Halogenwasserstoff (Hal· + RH → H-Hal + R·) außerdem die Reaktion der Melaminverbindung mit der Novolakmatrix.
    Notes: The photolysis of halogenophenol novolacs is determined by the substitution of halogens by hydrogen and the formation of quinoid groups and intermolecular crosslinks. This is concluded from elemental analysis, NMR, IR and optical absorption measurements. The rate of halogen release depends on the chemical nature of the halogen. It increases in the order F 〈 Cl 〈 Br 〈 I. Chlorine elimination from 4-position is favored over that from 2- and 3-position. Moreover, dimers release chlorine from 4-position much more readily than trimers and tetramers. ESR measurements at 77 K and flash photolysis studies at 296 K yielded evidence for the intermediate existence of phenoxyl and aryl radicals. Lithographic tests demonstrated the high UV-sensitivity of resist formulations based on halogen-containing novolacs. The increase in sensitivity relative to that of formulations based on nonhalogenated novolacs is 6 to 10fold system: 4-chlorophenol novolac/4,4′-bisazidobiphenyl (5%) and ca. 25fold system: 4-chlorophenol/m-cresol novolac/hexamethoxymethylmelamine (5%). A postulated reactions mechanism concerning the sensitivity increase takes into account that halogen elimination results in the formation of additional radicals that accelerate the rate of crosslinking. Moreover, hydrogen halide generated by hydrogen abstraction of halogen radicals (Hal· + RH → H-Hal + R·) provides for the acid required to catalyze the reaction of the melamine compound with the novolac matrix.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052140117
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  • 6
    Electronic Resource
    Electronic Resource
    Crystallization behavior of polypropylene filled with calcium carbonate of various shape (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 11-24 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Calciumcarbonate unterschiedlicher Teilchenform (sphäarisch, kubisch und nadelfäormig) wurden mit Polypropylen (PP) in einer Zwei-Walzen-Mäuhle gemischt und anschließend zu Platten gepreßt. Der Einflußder Teilchenform auf das Kristallisationsverhalten der PP/CaCO3-Composite, d.h. Kristallisationspeaktemperatur (Tmax), Kristallisationsverlauf usw., wurde mittels Differentialkalorimetrie untersucht. Der Wert von Tmax häangt von der Größe der Gesamtoberfläache der CaCO3-Teilchen ab; Tmax ist bei nadelfäormigen Teilchen gräoßer als bei kubischen oder sphäarischen und hauangt in allen Fäallen der nicht-isothermen Kristallisation von der Abkäuhlgeschwindigkeit und der vorher erreichten maximalen Temperatur ab.
    Notes: Calcium carbonate of various particle shape (spheric, cubic, needle-shaped type) and polypropylene (PP) were mixed on a two roll mill and the mixture was pressed into plates. The effect of particle shape on the crystallization behavior of PP/CaCO3 composites, such as crystallization peak temperature (TMAX), crystallized pattern, etc., was investigated with differential scanning calorimetry measurements. The value of TMAX is explained by the total surface area of added CaCO3 particles; TMAX of needle-shaped series is larger than that of cubic or spheric ones. TMAX of various shaped CaCO3-filled PP totally depends on the cooling rate and maximum temperature in the non-isothermal crystallization, respectively.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052150102
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  • 7
    Electronic Resource
    Electronic Resource
    Cationic polyelectrolytes, XIIPart. XI cf.8.. PEG-precursor for water-soluble cationic polymers with tertiary n-atoms in the main chain (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 107-119 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Polyaddition von Polyethylenglykol (PEG) Oligoglycidylethern (Mn (PEG): 396,587, 1437 und 3554) mit asymmetrischen Diaminen, wie N,N-Dimethylund N,N-Diethyl-1,3-diaminopropan, wurden wasserläosliche kationische Polymere erhalten. Die Eigenschaften der kationischen Polymeren sind vom urspräunglichen PEG-Molekulargewicht und der Diaminreaktivitäat abhäangig. PEG mit Mn = 396 zeigt das beste Verhalten. In verdäunnten wäassrigen Läosungen und in wäassrigen 2M NaCl-Läosungen der Polymeren wurde das Polyelektrolytverhalten veranschaulicht. Die Gegenwart der PEG Kette bestimmt das Polyelektrolytverhalten in den 2M NaCl Läosungen.
    Notes: Water-soluble cationic polymers were obtained by polyaddition of poly(ethylene glycol) (PEG) diglycidylethers (M̄n of PEG were 396, 587, 1437 and 3554, resp.) with asymmetrical diamines such as N,N-dimethyl-1,3-diaminopropane and N,N-diethyl-1,3-diaminopropane. The cationic polymer properties depend on the PEG initial molecular weight and on the diamine reactivity too. PEG with M̄n = 396 had the best behaviour in these reactions. The polyelectrolyte feature of cationic polymers was emphasized both in dilute aqueous solutions and in 2M aqueous NaCl solutions. The polyelectrolyte behaviour in 2M aqueous NaCl solution is determined by the PEG chain presence.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052150109
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  • 8
    Electronic Resource
    Electronic Resource
    Untersuchungen zur reaktion von o-kresol mit formaldehyd unter verwendung tertiärer amine (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 139-145 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Reaktion von o-Kresol mit Formaldehyd wurde unter Verwendung verschiedener tertiäarer Amine als Katalysatoren untersucht. Der Einfluß der Reaktionsparameter Basizitäat, Temperatur, Reaktionszeit und Formaldehydkonzentration wird diskutiert. Für die bevorzugte Bildung von 2,4-Bis(hydroxymethyl)-6-methylphenol wurden optimierte Synthesebedingungen erarbeitet. Die Bildung von Zwei-bzw. Mehrkernprodukten konnte nicht ausgeschlossen werden.
    Notes: The reaction between o-cresol and formaldehyde was investigated using various tertiary amines as catalysts. The influence of the reaction parameters basicity, temperature, reaction time and concentration of formaldehyde was discussed. To yield preferentially 2,4-bis(hydroxymethyl)-6-methylphenol the conditions of synthesis were optimized. The formation of bi- and polynuclear products cannot be avoided.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052150112
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  • 9
    Electronic Resource
    Electronic Resource
    Effect of addition of cellulose powder on the viscometric behavior of liquid crystalline solutions of ethyl cellulose in m-cresol (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 189-200 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Scherviskositäat fläussigkristalliner Ethylcellulose, die mit Cellulosepulver unterschiedlicher Partikelgräoße gefäullt war, wurde bei konstantem Schergefäalle mit einem Kegel-Platte-Viskosimeter bestimmt. Der Einfluß des Cellulosepulvergehalts, des Läange/Breite-Verhäaltnisses der Pulverteilchen und der Temperatur auf das viskose Verhalten und die Phasenäubergäange wird diskutiert. Der Zusatz von Cellulosepulver erhäoht die Viskositäat und verringert die Aktivierungsenergie des Fließens(Ea), ohne jedoch die Phasenäubergäange zu beeinflussen. Die Viskositäat und die Aktivierungsenergie sind abhäangig vom Läange/Breite-Verhäaltnis der Pulverteilchen; mit zunehmender Gräoße dieses Verhäaltnisses wird die Viskositäatszunahme beschleunigt und die Aktivierungsenergie des Fließens erhäoht, wäahrend die Aktivierungsenergie mit steigendem Pulvergehalt abnimmt. Die Phasenumwandlungen sind unabhäangig von der Partikelform. Der Einfluß des Pulvergehalts auf Viskositäat und Aktivierungsenergie ist abhäangig von der Art der fläussigen Phase; in der anisotropen Phase ist der Einfluß geringer als in der isotropen Phase. Dies scheint von der Ausrichtung der Pulverteilchen und der stäabchenfäormigen Molekäule herzuräuhren.
    Notes: Steady-state shear viscosity for the liquid crystalline ethyl cellulose solution filled with cellulose powders was determined using a cone-plate-type viscometer and the effects of cellulose powder content, powder aspect ratio and temperature on the viscometric behavior and phase transformation were discussed. The addition of powder increased the viscosity and decreased the activation energy (Ea) for flow, but did not affect the phase transformation. The viscosity and Ea depended on the aspect ratio; with greater aspect ratio, the viscosity enhancement was accelerated and Ea as well as the decrease in Ea with powder content increased. The phase transformation did not depend on the aspect ratio, the dependences of viscosity and of Ea on powder content depended on the solution phase; the dependences for the anisotropic phase were smaller than those for the isotropic one. The findings appeared to originate from the alignments of powders and rod-like molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052150116
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  • 10
    Electronic Resource
    Electronic Resource
    Oxygen uptake methods as a tool to determine the mechanism of action of hindered amine light stabilizers1Paper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 37-44 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The UV-degradation of an unstabilized and two HALS stabilized polyethylene (PE) films is described. The degradations are characterized by measuring the oxygen uptake, the formation of CO and CO2, the FT-IR spectra, the mechanical properties, the stabilizer concentration and the oxygen content of the film.The oxygen uptake of the unstabilized PE film led to the expected changes in the IR spectra and embrittlement of the film, while the oxygen uptake by the HALS stabilized films caused only minor changes. The differences between the results for the unstabilized and the HALS stabilized polymers are explained assuming that the initiation of the photodegradation of PE is due to charge transfer complexes.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052160103
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  • 11
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    Current of status of exploitation of radical scavenging stabilizers in advanced polymer stabilizationPaper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 135-146 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Principal chemical pathways characteristic of active participation of radical scavenging polymer stabilizers (phenols, aromatic, hydroaromatic and hindered aliphatic amines) are outlined. Pathways resulting in a partial depletion or distortion of activity of stabilizers, in formation of polymer discolouring products, or in interactions in bifunctional stabilizers are involved.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052160109
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  • 12
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    Poly(butyleneterephtalate) photolysis and photooxidation : Identification of the ir-absorbing productsPaper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 155-167 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Irradiations (λ≥300 nm) of poly(butyleneterphtalate) films were carried out in both vacum and air. Photoproducts were investigated by FTIR spectroscopy, chemical derivatization reactions and physical treatments. The repartition of photoproducts in the polymer was shown to be heterogeneous. A scheme accounting for the main routes of PBT photolysis was found on the basis of photoproducts identification. Most of oxidation products were analogous to vacum photolysis species; the mechanism of photooxidation proposed implied both pure photolytical processes and a photo-induced oxidation route.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052160111
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  • 13
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    Photo- and radiation-induced degradation of synthetic polymers: Polymer structure and stabilityPaper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 225-241 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of polymer density, processing conditions (quenching of annealing), degree of crystallinity, size of crystallite and mobility of polymer chains on the photo-and radiation-induced degradation and the polymer stability have been studied by UV, FTIR spectroscopic, viscosity and mechanical property measurements. Four kinds of annealed or quenched polyethylene (PE) films varying densities were used to the studies. Polystyrene (PSt) films were used to investigate the effect of chain mobility on polymer degradation. The following results were obtained. 1.In linear low density (LLD) PE, greater amounts of crosslinking (irradiated in vacuum) and chain scission (irradiated in air) were noticed than in mediun density (MD) PE and high density (HD) PE samples.2.Polyene formation is favored in the case of the irradiation in vacuum for LLDPE.3.Polymer stability evaluated by mechanical property such as elongation at break (%) is superior in LLDPE to MDPE and HDPE for annealed and quenched samples.4.Segmental motion of polymer chain also affects the polymer stability
    Additional Material: 19 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052160115
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  • 14
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    Eigenschaften von binären mischungen aus polyethylenen hoher dichte mit ultrahoher und normaler molmasse (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 43-49 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The study is on two component blends of high density polyethylenes, having normal and ultra-high molecular weight. The polyethylenes were homogenized by two routes: in powder state or by rolling in melt, then pressed at temperatures in the range from 140°C to 220°C. Comparative studies showed that the way of homogenizing of the components does practically not affect the main mechanical properties of the blends when pressed at temperatures ≥ 160°C. Of special interest are the characteristics of those systems where ultra-high molecular weight polyethylene is the matrix component.
    Notes: Untersucht wurden binäre Mischungen von Polyethylenen hoher Dichte rnit normaler und ultrahochmolekularer Molmasse, die auf zweierlei Weise - in Pulverform oder durch Walzen im Schmelzezustand - homogenisiert und bei Temperaturen zwischen 140 und 220°C gepreßt waren.Es wurde festgestellt, daß die Art der Homogenisierung der Komponenten praktisch keinen Einfluß auf die Eigenschaften bei Preßtemperaturen ≥ 160°C hat. Von besonderem Interesse sind die Eigenschaften der Systeme, in welchen das ultrahochmolekulare Polyethylen die Rolle der Matrixkomponente spielt.
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052170105
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    Rôle des pigments dans une réaction de polymérisation sous lumière UV-visible (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 81-109 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Verhalten eines neuartigen photoinitiierenden Systems, das die Polymerisation von pigmenthaltigen Schichten großer Dicke in einem Reaktionsschritt gestattet, wird dargestellt. Die verschiedenen Wechselwirkungen, die in einem pigmenthaltigen System auftreten, werden qualitativ beschrieben, und der Anteil der von einem Photoinitiator absorbierten Lichtintensität wird berechnet. Neben dem Absorptions- und Reflexionsverhalten von verschiedenen Pigmentklassen werden die optischen Eigenschaften verschiedener Strahlungsquellen untersucht, um die Strahlungsbereiche zu finden, die am besten mit den optischen Parametern der Pigmente korrespondieren. Weiterhin wird die Beschleunigung von Polymerisationen durch die photokatalytische Wirkung einiger Pigmente behandelt.
    Notes: Ce travail sur le rôe des pigments définit le comportement d'un nouveau systeme photosensible qui permet de polymériser des milieux épais et pigmentés selon un procédé en une seule étape. Les différentes interactions présentes en milieu pigmenté sont décrites de façon qualitative, et la part de l'intensité lumineuse absorbée par un photo-amorceur dans un systéme pigmenté est evaluée. Les propriétés optiques telles que l'absorption et la réflectance des différentes familles chimiques de pigments sont déterminées, et, en paralléle, les propriétés optiques des différentes sources d'irradiation sont étudiées de manière à répondre au mieux aux fenêtres de transmission des pigments. L'effet photocatalytique de certains pigments est mentionné, ceci afin d'amkliorer la réaction de polymérisation.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052180107
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    Molar mass distribution of polybutadiene synthesized with nickel-based Ziegler-Natta catalysts, I (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 153-162 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Herstellung von cis-1,4-Polybutadien erfolgte mittels Polymerisation von 1,3-Butadien mit einem Katalysatorsystem, das in einer zweistufigen Reaktion gebildet wird: (1) BF3 · O(C2H5)2 und Al(C2H5)3, (2) Ni(OOC8H15)2 und Al(C2H5)3, genannt in-situ-Katalysatorsystem.Die Molmassenverteilungen (MMD) der erhaltenen Polymeren sind mit der Größenausschlußchromatographie (SEC) untersucht worden. Sie lassen sich mit Summen aus Schulz-Flory-Funktionen (SFF) beschreiben. Veränderte Katalysatorformierungs- und Polymerisationsbedingungen beeinflussen die Parameter der SFF. Veränderte Peakflächen und Molmassenmittelwerte der Einzelpeaks zeigen, daß die Polymerisation über mehrere Arten aktiver Zentren verläuft.
    Notes: Cis-1,4-polybutadiene was produced by polymerization of 1,3-butadiene using a catalyst system formed by a two-step formation, Namely (1) BF3 . O(C2H5)2 and Al(C2H5)3, (2) Ni(OOC8H15)2 and Al(C2H5)3 named in-situ-catalyst.The molar mass distributions (MMD) of the polybutadienes are investigated by means of size exclusion chromatography (SEC). The MMD's were fitted by a sum of Schulz-Flory-Functions (SFF). Changed catalyst formation and polymerization conditions influenced the parameters of the SFF. Changed areas and changed molar mass averages indicate a polymerization with more than one peak maximum and kind of active species and lead to a better understanding of the polymerization.
    Additional Material: 9 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052180111
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    Synthesis and characterization of epoxy resins containing chromium acrylate (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 1-10 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Umsetzung von Chromacrylat mit Bisphenol A und einem Überschuß Epichlorhydrin wurden neuartige Epoxid-Harze hergestellt. Epoxy-Äquivalentgewicht, Gehalt an Hydroxygruppen und hydrolysierbarem Chlor sowie die Viskosität wurden bestimmt, und die Harze wurden mittels IR- und 1H-NMR-Spektroskopie charakterisiert. Die thermischen Eigenschaften der bei 30°C für 24 h mit Ciba Geigy HY 850 (aliphatisches Amin) gehärteten Harze wurden gemessen. Die Harze besitzen eine gute thermische und chemische Stabilität und eine gute elektrische Leitfähigkeit. Die Reaktion verläuft nach erster Ordnung; die Aktivierungsenergie beträgt 47 kJ mol-1 bzw. 34 kJ mol-1 mit bzw. ohne Chromacrylat. Aus spektroskopischen Untersuchungen wird geschlossen, daß das Chrom mit Bisphenol A einen Komplex bildet, der die Epoxidierung beschleunigt.
    Notes: Novel epoxy resins containing chromium acrylate have been synthesized by reacting chromium acrylate with bisphenol-A and excess epichlorohydrin. The quantities such as epoxy equivalent weight, hydroxy content, hydrolyzable chlorine content and viscosity have been determined. The resins have been characterized by IR and 1H NMR spectroscopy. The cured resins were evaluated for thermal properties. The curing of resins was carried out with Ciba Geigy HY 850 (aliphatic amine adduct) at 30°C for 24 h. The cured resins have excellent thermal and chemical resistance, in addition to an excellent electrical conductivity. The reaction follows first order kinetics with an activation energy of 47 kJ mol-1 and 34 kJ mol-1 in the presence and absence of chromium acrylate, respectively. The chromium forms a complex with bisphenol-A, as indicated by spectroscopic studies, which increases epoxidation.
    Additional Material: 6 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052190101
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    Interpenetrating polymer networks based on liquid natural rubber. 1. Synthesis and effect of nco/oh ratio on physical and mechanical properties (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 67-76 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Interpenetrierende Polymernetzwerke (IPNs) aus Polystyrol und Polyurethan auf der Basis von hydroxyterminiertem Naturkautschuk mit unterschiedlichen NCO/OH-Verhältnissen wurden unter verschiedenen Reaktionsbedingungen hergestellt und zu widerstandsfähigen Filmen verarbeitet. Die IPNs wurden durch ihre physikalischen, mechanischen und morphologischen Eigenschaften wie Dichte, Shore-A-Härte, Vernetzungsdichte, Zugfestigkeit und Reißdehnung charakterisiert. Mit steigendem Polystyrolgehalt erhöhen sich auch Dichte, Shore-A-Härte und Zugfestigkeit, während die Reißdehnung abnimmt. Die Untersuchungen der Vernetzungsdichte lassen eine Phasenumkehr vermuten.
    Notes: Interpenetrating polymer networks (IPNs) of polyurethane based on hydroxyterminated natural rubber with varying NCO/OH ratios and polystyrene were synthesized under different experimental conditions. These IPNs were found to make tough films. The IPNs were characterized by their physical, mechanical and morphological properties like density, Shore-A hardness, crosslink density, tensile strength and elongation at break. The IPNs exhibited an increasing trend in density, Shore-A hardness and tensile strength with increasing polystyrene content, while elongation at break decreased with similar variation in polystyrene content. The crosslink density measurements indicated a possible phase inversion process.
    Additional Material: 7 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052190106
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    Plasma treatment of polyethylene ultrafiltration membranes (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 117-124 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß einer Plasmabehandlung von Ultrafiltrationsmembranen aus Polyethylen auf die Fouling- und Reinigungseigenschaften bei der Filtration von Rinderserumalbumin werden diskutiert. Bei 2,45 GHz erzeugtes Luft-Plasma steigert die Hydrophilie der Membranoberfläche von 0 auf 60%. Der Durchfluß bleibt bei 90 bis 99%. Mit Plasma behandelte Membranen sind leichter zu reinigen als unbehandelte; dennoch sind sie anfälliger für die Ablagerung von Rinderserumalbumin.
    Notes: The effect of plasma treatment of polyethylene ultrafiltration membranes on fouling and cleaning phenomena during filtration of bovine serum albumin solutions is discussed. Air-plasma of 2.45 GHz raises the membrane surface hydrophilicity from 0 up to 60%. The flux is maintained at 90-99%. Plasma-treated membranes are easier to clean than untreated polyethylene membranes. Despite that, the plasma-modified membranes are susceptible to more intensive deposition of albumin.
    Additional Material: 4 Tab.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052190110
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    Preparation and characteristics of immobilized glucose oxidase on membranes of photosensitive polymers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 101-115 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Immobilisierung von Glucose-Oxidase in einer Poly(vinylalkohol) (PVAL)-Membran in Gegenwart von UV-Photoinitiatoren wurde untersucht. Enzym-Membranen wurden aus PVAL-Diazoharz- und PVAL-Photoinitiator-Systemen durch Vernetzung mit UV-Licht hergestellt. Mit diesen immobilisierten Glucose-Oxidase-Membranen wurde eine wirkungsvolle Enzymelektrode entwickelt, deren Eigenschaften untersucht wurden. Der Einfluß der Photoinitiatorkonzentration in Poly(vinylalkohol) und der UV-Bestrahlungsdauer auf den Grad der Unlöslichkeit sowie die Aktivitätsausbeute der Membran wurden mit Glucose als Substrat untersucht. Temperatur- und pH-Abhängigkeit der relativen Aktivität, Stabilität bei mehrmaligem Gebrauch, Lagerstabilität und Kalibrierungsdiagramme der Enzym-Membranen wurden ermittelt. Eine beim Erstgebrauch auftretende Instabilitätserscheinung der Membranen wurde ebenfalls untersucht.
    Notes: A study of the immobilization of glucose oxidase on a poly(vinyl alcohol) (PVAL) membrane in the presence of UV sensitizers was carried out. Enzyme membranes were prepared from PVAL-diazoresin and PVAL-sensitizer systems, crosslinked by means of UV irradiation. An effective enzyme electrode was developed by using the immobilized glucose oxidase membrane, and its characteristics were investigated. The effects of the concentration of sensitizers in poly(vinyl alcohol) and UV irradiation time on the degree of insolubility as well as the activity yield of the membrane were examined for the immobilized glucose oxidase using glucose as a substrate. Temperature and pH dependences of the relative activity, stability in repeated use, storage stability and calibration plots of the enzyme membranes were evaluated. The unstability phenomenon, found in the initial use of the immobilized glucose oxidase membrane, which was prepared from PVAL-sensitizer system, was also investigated.
    Additional Material: 11 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052190109
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    Auswirkungen von Sterilisationsverfahren auf biologisch abbaubare Kunststoffe (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 11-26 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Biopol, Biocellat and Mater-Bi, three biologically decomposable plastics have been tested for their use in medical industries. Biopol did not loose its stress and stiffness under sterilisation, and was also resistant against temperature and alcohol. Mater-Bi and Biocellat, the two other materials, did not satisfy the test applications. Water vapor sterilisation, temperature up to 60°C, at higher temperatures this material will embrittle.
    Notes: Für den Einsatz biologisch abbaubarer Kunststoffe in der pharmazeutischen Industrie und Medizintechnik wurden Produkte verschiedener Hersteller, wie Biopol, Biocellat und Mater-Bi untersucht. Dabei zeigte vor allem Biopol das notwendige Anforderungsprofil, d.h. die Anwendbarkeit aller Sterilisationsverfahren ohne Festigkeitsbzw. Steifigkeitsverluste sowie Temperatur- und Alkoholbeständigkeit. Dagegen wiesen die Werkstoffe Mater-Bi und Biocellat einige Schwachstellen auf. Bei Mater-Bi lagen diese bei der Wasserdampfsterilisation sowie bei der geringen thermischen und Medienbeständigkeit. Biocellat versprödet dagegen durch die erhöhte Temperatur bei der Dampfsterilisation, d.h. daß ein Einsatz über 60°C nicht möglich wäre.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1994.052190102
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    Polymers and copolymers based on vinyl tetrazoles, 2Part 1 cf.10.. Alkylation of poly(5-vinyl tetrazole) (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 89-99 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Alkylierung von Poly(5-vinyltetrazol) mit Dimethylsulfat und tert-Butylalkohol sowie Alkylhalogeniden RHal (R=CH3, C2H5, CH2—CH=CH2, n-C4H9 und t-C4H9) und die Kinetik dieser Reaktion wurden untersucht, um eine neue Herstellungsmethode für tetrazolhaltige Polymere mit wertvollen Eigenschaften zu entwickeln. Die vergleichenden Untersuchungen über die isomere Zusammensetzung und die spektroskopischen Daten von Poly(N-alkyl-5-vinyltetrazol)en, die durch die Alkylierung von Poly(5-vinyltetrazol) sowie durch die Copolymerisation der entsprechenden Monomeren hergestellt wurden, wurden mit IR-, 1H-NMR- und 13C-NMR-Spektroskopie durchgeführt. Der Alkylierungsumsatz beträgt bis zu 99,8%; dadurch können polymere Produkte erhalten werden, deren Zusammensetzung, Struktur und Eigenschaften denen der Homo- und Copolymeren sehr ähnlich sind.
    Notes: Alkylation of poly(5-vinyl tetrazole) with dimethyl sulfate and tert-butyl alcohol as well as with alkyl halides RHal (R=CH3, C2H5, CH2—CH=CH2, n-C4H9, t-C4H9) has been studied under various conditions in order to develop a new method of synthesis of tetrazole-containing polymers having a complex of valuable properties. The kinetic study of the process and comparison of isomeric compositions and spectroscopic characteristics (IR, 1H NMR and 13C NMR) of poly(N-alkyl-5-vinyl tetrazole)s synthesized by alkylation of poly(5-vinyl tetrazole) and of those prepared by (co)polymerization of the corresponding vinyl tetrazoles have been carried out. The alkylation is found to proceed to high conversion extents (up to 99.8%) and enables to obtain a wide variety of polymeric products having the composition, structure and properties very similar to those of homo- and copolymers.
    Additional Material: 1 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052190108
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    Dyes for nonlinear optics prepared from 2-hydroxyethyl methacrylate. Nonlinear properties of the resulting copolymers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 75-87 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Farbstoffe mit nichtlinearen optischen Eigenschaften wurden in einer zweistufigen Synthese aus 2-Hydroxyethylmethacrylat (HEMA), 4-Carboxybenzaldehyd und verschiedenen Anilinderivaten hergestellt. Die Farbstoffe (aromatische Iminester von HEMA) wurden mit Styrol copolymerisiert, die erhaltenen Copolymere wurden mit DSC sowie IR-, 1H NMR- und UV-VIS-Spektroskopie charakterisiert, und ihre nichtlinearen Eigenschaften wurden untersucht. Es zeigte sich, daß die nichtlinearen Koeffizienten d31 und d33 vom Farbstoffgehalt der Copolymeren und der Art der elektronenspendenden Gruppen abhängig sind.
    Notes: Dyes for nonlinear optics have been synthesized in two steps from 2-hydroxyethyl methacrylate (HEMA), 4-carboxybenzaldehyde and various substituted anilines. The obtained dyes (aromatic imine esters of HEMA) have been copolymerized with styrene, the copolymers characterized by DSC as well as IR, 1H NMR and UV-VIS spectroscopy, and studied for their nonlinear properties. The d31 and d33 nonlinear coefficients proved to be dependent on the dye content of the copolymers and on the nature of electrondonating groups.
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052200107
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    Viscosity behaviour of multivalent metal ion-containing carboxymethyl cellulose solutions (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 123-132 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß von Ca2+-bzw. Al3+-Ionen auf das Viskositätsverhalten (Salzverträglichkeit) wäßriger Lösungen von Natriumcarboxymethylcellulose (CMC) sowohl mit unterschiedlichem Polymerisationsgrad (DP) als auch mit unterschiedlichem Substitutionsgrad (DS) und verschiedenartiger Substitutentenverteilung wurde untersucht. Aus Viskositätsmessungen mit einem Rotationsviskosimeter bei einer Scherrate von 500 s-1 geht hervor, daß die relative Abnahme der Viskosität im Ergebnis des Zusatzes der mehrwertigen Metallkationen unabhängig vom DP (im Bereich von 160 bis 900) der CMC ist. Homogen hergestellte CMC-Proben 2 mit einem größeren Gehalt an 2,3,6-Tri-O-carboxymethylglucose-Einheiten in der Polymerkette weisen im Vergleich zu heterogen hergestellten CMCs 1 bei gleichem Gesamt-DS eine höhere Salzverträglichkeit auf.
    Notes: The influence of Ca2+-and Al3+-ions, respectively, upon the viscosity behaviour (so-called salt tolerance) of aqueous solutions of sodium carboxymethyl cellulose (CMC) with different degree of polymerization (DP) and, on the other hand, with both different degree of substitution (DS) and distribution of substituents, was investigated. Viscosimetry by means of a rotational rheometer at a shear rate of 500 s-1 shows that the relative drop in viscosity as a result of addition of the multivalent metal cations is independent of DP (ranging from 160 to 900) of the CMC samples. Homogeneously synthesized CMCs (2) with a higher content of 2,3,6-tri-O-carboxymethyl glucose units in the polymer chain possess a significantly higher salt tolerance than those (1) prepared under heterogeneous reaction conditions at comparable total DS values.
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052200111
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    Modification of melamine-formaldehyde moulding compounds with ethylene/vinyl acetate copolymers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 61-87 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Melamin-Formaldehyd-Harz-Formmassen (MF) wurden durch mechanisches Mischen mit Ethylen-Vinylacetat-Copolymeren (EVA) und teilverseiftem EVA modifiziert, wobei Etherbindungen zwischen dem hydrolysierten EVA und dem MF-Harz nachgewiesen werden konnten, die die mechanischen Eigenschaften von spritzgepreßten Formteilen im Vergleich zur Modifizierung mit EVA verbessern. Der Zusatz solcher Modifikatoren erhöht die Duktilität und verringert im Falle von EVA die Nachschwindung der überaus steifen MF-Matrix, solange der Modifikatoranteil gering bleibt. Dagegen werden die Steifigkeit und die Wärmeformbeständigkeit verschlechtert. Die durch solche unvernetzten Polymeren erreichbare Steigerung der Schlagzähigkeit bleibt allerdings unzureichend.
    Notes: Melamine-formaldehyde moulding compounds (MF) were modified by mechanical mixing with ethylene/vinyl acetate copolymers (EVA) and with partially hydrolysed EVA. Ether linkages between the hydrolysed material and the MF resin improve the mechanical properties of the transfer moulded parts containing the hydrolysed material compared to those made with EVA. The use of both modifying polymers improves the ductility and, in case of the partially hydrolysed material, the postshrinkage of the extremely rigid MF matrix, as long as the modification polymer content is kept low. On the contrary, Young's modulus and the heat deflection temperature are deteriorated. The improvement in impact strength by use of those uncrosslinked polymers is still insufficient.
    Additional Material: 17 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052220106
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    Synthesis and properties of biodegradable copolyesteramides: Nylon 6,6/∊-caprolactone copolymers, 1 (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 111-123 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Eine Reihe von Copolyesteramiden mit Molekulargewichten zwischen 1000 und 7000 (GPC, NMR) wurden aus Adipinsäure/1,6-Hexandiamin/∊-Caprolacton bzw. Nylon 6,6-Salz/∊-Caprolacton hergestellt. Die thermischen Eigenschaften der synthetisierten Polymeren (Glasübergangs-, Schmelz-, und Zersetzungstemperaturen, Schmelzenthalpien) wurden durch DSC- und TGA-Messungen bestimmt und in Bezug auf das Comonomerverhältnis in der Ausgangsmischung diskutiert. Die Übereinstimmung der Copolymerzusammensetzung mit dem Ausgangscomonomerverhältnis wurde mit FT-IR- und NMR-Spektroskopie untersucht. Die Bioabbaubarkeit der Copolyesteramide wurde durch enzymatische Hydrolyse geprüft.
    Notes: A series of copolyesteramides based on adipic acid/1,6-hexane diamine/∊-caprolactone and Nylon 6,6 salt/∊-caprolactone were synthesized. Their molecular weights, determined by gel permeation chromatography and NMR spectroscopy, were found to lie within the range from 1000 up to 7000. Their thermal properties (glass transitions, melting points and heats of melting, and decomposition temperatures) were recorded with diferential scanning calorimetry and thermogravimetry, respectively, and correlated to the comonomer feed composition. The FT-IR and NMR spectra were also recorded in order to confirm the composition of the copolyesteramides and to compare them with that of the comonomer feed. The biodegradability of the synthesized copolymers was tested by enzymatic hydrolysis.
    Additional Material: 4 Ill.
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    Study of the condensation products of abietic acid with formaldehyde at high temperatures (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 165-174 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch sulfonsäurekatalysierte Umsetzung von Abietinsäure und Paraformaldehyd bei hohen Temperaturen wurden neuartige Kondensationsprodukte erhalten. Als Nebenprodukte der Polykondensation werden eine Ketoverbindung sowie Wasser und Kohlendioxid gebildet. Die Carboxygruppen der Abietinsäure sind an der Kondensationsreaktion beteiligt. In Abwesenheit von Paraformaldehyd wurde das Abietinsäure/Sulfonsäurekatalysator-System untersucht, um zusätzliche Informationen über die Reaktion zu erhalten. Der Reaktionsverlauf hängt von der Temperatur und der chemischen Struktur des Katalysators ab. Ein möglicher Reaktionsmechanismus der Kondensation wird diskutiert.
    Notes: New condensation products have been synthesized by heating abietic acid and formaldehyde at high temperatures in the presence of sulfonic-type acid catalysts. The main polycondensation reaction is associated with a secondary one which leads to a ketonic compound, carbon dioxide and water. The carboxylic groups of abietic acid participate in this condensation reaction. The behaviour of the abietic acid-sulfonic acid catalyst system was studied in absence of formaldehyde to acquire additional information about the reaction. The process is defined by the reaction temperature and chemical nature of the catalyst. A possible mechanism of the condensation reaction is discussed on the basis of the obtained results.
    Additional Material: 2 Ill.
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    Tailored polymers by cationic ring-opening polymerization (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 1-11 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: After a general classification of the cationic ring-opening polymerizations (CROP's) according to their polymerization mechanism, a number of examples of tailored polymers based on CROP are presented. The monomers used for the synthesis of these tailored structures are tetrahydrofuran (THF), N-tert-butyl aziridine (TBA), 2-methyl-1,3-oxazoline (MeOX) and 1,3-dioxolane (DXL).The polymer structures include different block and graft copolymers, macromonomers, star-shaped polymers, polymer networks and interpenetrating polymer networks (IPNs).
    Additional Material: 1 Tab.
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    Massgeschneiderte PolymereVortrag anläßlich der Tagung der Fachgruppe “Makromolekulare Chemie” der Gesellschaft Deutscher Chemiker über “Fortschritte in der Polymersynthese” in Bad Nauheim, 21.-22. März 1994. Synthesestrategien für Telechele, Makromonomere, Block- und Pfropfcopolymere (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 29-46 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: In diesem Beitrag wird ein überblick über neuere Entwicklungen auf dem Gebiet der Synthese von Telechelen, Makromonomeren, Block- und Pfropfcopolymeren gegeben. Synthesestrategien aus den Bereichen der Polykondensation, der radikalischen, anionischen und kationischen Polymerisation, der Kettenspaltung sowie der Criss-Cross-Cycloaddition werden diskutiert.
    Notes: New developments in the synthesis of telechelics, macromonomers, block- and graftcopolymers are presented. Synthetic strategies for them are demonstrated with examples from different fields such as polycondensation, radical, anionic, and cationic polymerization, chain cleavage and criss-cross-cycloaddition.
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    Alkane als initiatoren zur radikalischen polymerizationHerrn Professor Dr. rer. nat. Dr.-Ing. E.h. Hansjörg Sinn mit den besten Wünschen zum 65. Geburtstag gewidmet (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 69-79 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Alkanes with highly substituted carbon-carbon bonds can be cleaved in free radicals by homolytic dissociation under the influence of thermal energy. The energy of dissociation is mainly determined by the type and size of the respective substituents. For tetraarylbutane dinitriles the temperatures of decomposition are in the range of other technically used initiators. But nevertheless, these compounds are up to now rather seldom used to initiate free radical polymerizations. This is connected with the special mechanism of initiation: the formed highly substituted alkyl radicals are relatively stable and show only a rather low reactivity against the usually used monomers. Therefore, in the beginning of the polymerization the radical concentration is rather high which leads not only to addition to monomers but also to a pronounced primary radical termination. In some cases this termination process is reversible which results in an unusual polymerization kinetics. Depending on the type of monomer and the degree of reversibility of the primary radical termination, either a period of “dead-end” polymerization follows or the cleavage of the oligomers at the chain end results in a re-initiation process with a “normal” polymerization with increased rate. The reaction mechanism, kinetics and some possible applications of such initiating alkanes are reported.
    Additional Material: 3 Ill.
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    Cycloolefin-copolymere: Eine neue klasse transparenter thermoplasteHerrn Prof. Dr. H. Sinn zum 65. Geburtstag gewidmet. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 121-133 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Untersuchungen wesentlicher Aspekte der Polymerisation und der Eigenschaftsmodifikation auf Metallocen-Katalyse basierender Cycloolefin-Copolymere (COC) zeigen, daß mit dieser Monomer-Katalysator-Kombination eine neue Klasse transparenter Thermoplasten zugänglich gemacht wird. COC können mit Metallocenen in beliebiger zusammensetzung und mit kontrollierter Mikrostruktur hergestellt werden. Die somit erreichte und durch zusätzliche Modifikationen noch erweiterbare Breite des Eigenschaftsspektrums ermöglicht vielfältige Anwendungen dieser neuen Polymerklasse. Die wichtigsten Schlüsselfaktoren im rohstofflich-technologischen Bereich, die diese Struktur- und Eigenschaftsvielfalt ergeben, werden beispielhaft beschrieben.
    Notes: Investigation of the polymerization process and property modification of metallocene-based cycloolefin copolymers (COC) shows that this monomer-catalyst combination enables synthesis of a new class of transparent thermoplastic polymers. Metallocene catalysis offers much opportunity to vary the composition and microstructure of the copolymers. The breadth of the polymer spectrum which can be further widened by polymer modification enables many applications for this new class of thermoplastics. The key parameters that control structure and properties in the COC family are discussed in this paper.
    Additional Material: 6 Ill.
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    Funktionalisierte Kammpolymere: Synthesen, modifizierung und anwendungen (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 165-175 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The present paper deals with the synthesis and modification of functionalized polymers characterized by a special molecular architecture. The reactivity of a functionalized polymer with comb-like structure can be controlled in a significant manner by the crystalline order of the side chains. In contrast, photocrosslinking of comblike polymers containing cinnamic components in the side chains influences the crystallization process. The air drying process of a modified polybutadiene system with comb-like structure was shown to depend sensitively on the side chain order. Enzymatic synthesis of new monomers and polymers is briefly reviewed. The complexing capability of cyclodextrines were used to synthesize polyrotaxanes. Finally, the synthesis of a chiral polymerizable dendrimer containing eight estergroups in the monomer unit is presented.
    Additional Material: 8 Ill.
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    Intramolekular vernetzte poly(organosiloxan)partikel (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 203-216 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Intramolecularly crosslinked poly(organosiloxane) particles are prepared by means of emulsion polycondensation or emulsion polymerization of alkoxysilanes or cyclic organic siloxanes. Starting from these intramolecularly crosslinked poly(organosiloxane) particles, graft copolymers are obtained by free-radical emulsion polymerization of unsaturated olefinic monomers (e.g. acrylates, styrene) in the presence of (functionalized) organosiloxanes. Intramolecularly crosslinked poly(siloxane) particles and their graft copolymers are characterized by means of light scattering (in dispersion), electron microscopy and thermal analyses (DSC, DMTA).
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052230115
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    Study on poly(2,6-dimethyl-1,4-phenylene oxide)/SBS triblock copolymer blends (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 153-167 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Zusammenhang zwischen der Mischbarkeit und den physikalischen Eigenschaften von Polymerblends aus Poly(2,6-dimethyl-1,4-phenylenoxid) (PPO), die in unterschiedlichen Zusammensetzungen in einem Doppelschneckenextruder mit Polystyrol, schlagzähem Polystyrol oder Styrol-Butadien-Copolymeren hergestellt wurden, wird diskutiert. Die Verträglichkeit der Komponenten wurde mittels DSC und DMA, die Morphologie der Blends mittels SEM untersucht. Mit abnehmendem Polystyrolanteil wurde eine schlechtere Mischbarkeit bei den Blends beobachtet, deren Kerbschlagempfindlichkeit sich erhöhte. Die Untersuchungsergebnisse werden mit dem Micellmodell interpretiert.
    Notes: The relationship between the miscibility and the physical properties of polymer blends of poly(2,6-dimethyl-1,4-phenylene oxide) and polystyrene (PS), high-impact polystyrene (IPS) and poly(styrene-block-butadiene-block-styrene) (SBS), which are blended in different compositions by a twin-screw extruder is discussed. The three types of SBS that were used are SBS1, SBS2 and SBS3 having different styrene/butadiene ratios. Dynamic mechanical analysis and differential scanning calorimetry were used to study the miscibility. The morphology was examined by SEM. The miscibility of the blends decreases with decreasing PS content. The notch sensitivity is improved by blending. Finally, the micelle model was used to explain the testing phenomena.
    Additional Material: 8 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052140114
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    Water-soluble polyamides as potential drug carriers, VIIPresented in part at the Symposium on Water-soluble Polymers, 198th National Meeting Am. Chem. Soc., Miami Beach, Florida, 10-16 September 1989. For Part VI, cf1.. Synthesis of polymers containing intrachain- or extrachain-type amine ligands by interfacial polymerization (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 137-152 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Aliphatische Polyamide mit Poly(ethylenoxid)-Kettensegmenten unterschiedlicher Länge wurden durch Grenzflächenpolymerisation aus Succinylchlorid und Jeffamine ED-900 (O,O'-Bis(2-aminopropyl)poly(ethylenglykol) 800) bzw. Jeffamine ED-2001 (O,O'-Bis(2-aminopropyl)poly(ethylenglykol) 1900) zur Verwendung als Trägersubstanzen für Medikamente synthetisiert. Copolyamide mit kurzkettigen Diamin- und Jeffamine-Segmenten sowie Polyamide aus Cystin und Diamineinheiten wurden auf die gleiche Weise hergestellt. Die Polymerisationen wurden im zweiphasigen System Dichlormethan/Wasser bei Temperaturen um 0°C durchgeführt. Die Polymerprodukte wurden durch stufenweise Dialyse in wäßriger Phase bis zu einem Molekulargewicht von 25000 fraktioniert, nach Gefriertrocknung als wasserlösliche Harze oder Feststoffe erhalten und durch Mikroanalyse sowie 1H NMR-Spektroskopie charakterisiert. Die inhärenten Viskositäten liegen im Bereich von 10-20 ml/g. Die Eignung eines repräsentativen Zielmoleküls zur Bindung von Medikamenten wurde durch eine kovalente Verankerung einer als Medikamentmodell fungierenden Ferrocen-Verbindung untersucht. Dabei wurde ein wasserlösliches Polymer-Ferrocen-Konjugat erhalten.
    Notes: Aliphatic polyamides comprising poly(ethylene oxide) chain segments of various lengths, designed for use as drug carriers, are synthesized by interfacial polymerization of succinyl chloride with the two Jeffamine types ED-900 and ED-2001, formally described by the supplier as O,O'-bis(2-aminopropyl)poly(ethylene glycol) 800 and O,O'-bis(2-aminopropyl)poly(ethylene glycol) 1900. Copolyamides comprising both short-chain diamine and Jeffamine segments are similarly prepared, as are polyamides made up of cystine and diamine segments. The polymerizations are performed in a two-phase methylene chloride-water system at temperatures near or below 0°C. The product polymers, crudely fractionated by staged aqueous-phase dialysis at an ultimate molecular-mass cut-off of 25000, are collected after freeze-drying as water-soluble resins or solids and are characterized microanalytically and by 1H NMR spectroscopy. Inherent viscosities are in the range of 10-20 ml g-1. The drug-binding potential of a representative target polymer is probed by the covalent anchoring of a ferrocene compound used as a drug model, giving a water-soluble polymer-ferrocene conjugate.
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    Studies on vinyl ester resin and its urethane derivative as coating materials (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 211-216 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Über die Anwendung von Vinylesterharzen aus dem Diglycidylether von Bisphenol A sowie dessen Urethanderivat als Beschichtungsmaterial wird berichtet. Die mit den Harzen beschichteten Flußstahlplatten wurden auf Oberflächenglanz, Kratzfestigkeit und Chemikalienbeständigkeit untersucht. Harze mit Styrolanteil zeigen deutlich verbesserte Beschichtungseigenschaften.
    Notes: The present paper is concerned with the coating applications of a vinyl ester resin derived from diglycidyl ether of bisphenol-A and its urethane derivative. The mild steel panels coated with the synthesized resins were evaluated for their gloss on the surface, scratch hardness and chemical resistance. The incorporation of styrene in the resin systems improves the properties of coatings remarkably.
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    Silica gel supported zirconocene dichloride/methylalumoxane catalysts for ethylene polymerization: Effects of heterogenation on activity, polymer microstructure and product morphology (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 47-57 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Katalysatorsystem Zirkonocendichlorid/Methylalumoxan wurde auf Siliciumdioxid aufgebracht, um Katalysatoren fur die Suspensions- order Gasphasenpolymerisation von Ethylen herzustellen. Die häochste Aktivitäat wurde für eine sandwichartige, dreilagige Verankerung von Zirkonzentren auf der Träageroberfläache gefunden. Dieneuen Katalysatorsysteme besitzen eine im Vergleich zu den entsprechenden homogenen Katalysatoren geringere Aktivitäat. Die Immobilisierung der aktiven Katalysatorzentren führt zu einer deutlichen Erhäohung der Polymermolmassen. Dabei bleibt die enge Molekulargewichtsverteilung der Polymerprodukte nahezu erhalten. Solche auf Träager aufgebrachte Metallocen-Katalysatoren käonnten für die Herstellung von Polyethylenen mit kontrollierter Rheologie Anwendung finden.
    Notes: The system zirconocene dichloride/methylalumoxane was supported on silica in order to provide ethylene polymerization catalysts for suspension or gas phase processes. Highest activity was found for a sandwich-like, three layer anchoring of the zirconium centers on the support surface. The new catalyst systems show a decrease of activity compared to polymerization experiments in homogeneous phase. However, the molecular weights are increased and the weight distributions remain narrow by immobilization of the active catalyst sites. Those supported metallocene catalysts could find application for the synthesis of polyethylene materials with controlled rheology.
    Additional Material: 3 Ill.
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    Evaluation of poly(butyl acrylate-co-ethylene glycol dimethacrylate) sorbents for chromatographic separation of biomolecules (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 129-138 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Vernetzte Copolmere aus Butylacrylat (BA) und Ethylenglycol-dimethacrylat (EGDMA) wurden auf ihre Eignung als stationäare Phase für die Chromatographie untersucht. Es wurde festgestellt, daß gering vernetzte Copolymere (〈 30 Gew.-% EGDMA) nicht poräos sind, wäahrend Matrices mit mehr als 40 Gew.-% EGDMA eine konstante Porositäat aufweisen. Eine Erhäohung des Vernetzergehaltes beeinflußt hauptsäachlich die Hydrophobie der Oberfläache. Zwei Meßmethoden für diese Eigenschaft werden diskutiert: Die Absorption von Alkylalkoholen und von Aminosäauren. Für letztere wurde aus der Steigung der Beziehung zwischen der Sälenkapazitäat und dem Hydrophobie-Parameter der Aminosäauren ein Matrix-Hydrophobie-Index berechnet und dieser mit den bekannten Energien der Wechselwirkung von Alkylalkohol—CH2 Gruppen mit der Polymermatrix verglichen. Die Vorteile der Verwendung des Hydrophobie-Indexes bei der Bewertung von polymeren Sorbentien werden aufgezeigt.
    Notes: Copolymers of butyl acrylate (BA) crosslinked with ethylene glycol dimethacrylate (EGDMA) were evaluated as potential chromatographic packings. It was found that slightly crosslinked copolymers (up to 30 wt.-% EGDMA) did not provide porous material, while for matrices which exceeded 40 wt.-% of EGDMA the porous structure remained unchangeable. The increase of crosslinker content mostly affected the surface hydrophobicity. Two methods of measurement of this property were discussed: Sorption of alkyl alcohols and amino acids. Taking the latter for testing, a polymer matrix hydrophobicity index was calculated as the slope of dependence of column capacity vs. amino acid hydrophobicity parameter. The indices were verified against well-established interaction energies of —CH2— groups of alkyl alcohols and polymer surfaces. Some benefits of the use of the hydrophobicity index in evaluation of polymer sorbents were demonstrated.
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    Epoxysiloxane resins by the condensation of 3-glycidyloxypropyltrimethoxysilane with diphenylsilanediolDedicvated to Prof. Dr. Dr.-Ing. E. h. Hansjörg Sinn on the occasion of his 65th birthday (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 111-126 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kondensation von 3-Glycidyloxypropyltrimethoxysilan I mit Diphenylsilandiol II wurde untersucht. Abhängig von Lösungsmittel, Temperatur und Katalysator werden unterschiedliche Primärprodukte erhalten. Die Reaktion in Masse bei 120°C mit Titan(IV)-isopropylat als Katalysator liefert ein transparentes Harz A. Das eduktfreie Produkt wurde IR-, 1H- und 13C-NMR-spektroskopisch charakterisiert und chromatographisch mit GPC und HPLC untersucht. Die trimeren und tetrameren Siloxane bestehen aus Diphenylsilan- und 3-Glycidyloxypropylmethoxysilaneinheiten. Das Verhältnis von cyclischen zu linearen Molekülen beträgt 2:1. Höhermolekulare Verbindungen entstehen nur in geringen Mengen. Das Epoxysiloxangemisch löst sich in unterschiedlichen organischen Lösungsmitteln und ist mit kommerziell verfügbaren Epoxiden mischbar. Die Zeitabhs̈ngigkeit von Viskosität und Epoxidwert bei der Lagerung unter Normalbedingungen wurden gemessen und mit HPLC verfolgt . Die Lagerstabilität wurde durch eine zusätzliche thermische Behandlung verbessert.
    Notes: Condensation of 3-glycidyloxypropyltrimethoxysilane I with diphenylsilanediol II was investigated. Depending on solvent, temperature and catalyst, different products were obtained. Bulk reaction at 120°C using titanium(IV)-isopropylate as a catalyst provided the transparent resin A. A was characterised by IR, 1H- and 13C-NMR spectroscopy and contained no reactants. GPC and HPLC studies revealed that A consists of trimer and tetramer siloxanes of pertinent diphenylsilane and 3-glycidyloxypropylmethoxysilane moieties. The proportion of cyclic to linear molecules was evaluated 2:1. Only small amounts of high-molecular-weight compounds were observed. The epoxysiloxane product proved to be miscible with various organic solvents and with commercial epoxy resins. Time dependence of viscosity and epoxy content were recorded during ambient storage and monitored by HPLC. Pot-life was improved by a subsequent thermal procedure.
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    Molar mass distribution of polybutadiene synthesized with nickel-based Ziegler-Natta catalysts, IIPart I cf.14. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 163-170 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Cis-1,4-Polybutadien wurde durch Polymerisation von 1,3-Butadien mit Katalysatorsystemen hergestellt, die Ni(OOC8H15)2 und Al(C2H5)3 sowie die Lewissäuren BF3 · O(C2H5)2 oder TiCl4 enthalten. Die Molmassenverteilungen (MMD) der erhaltenen Polybutadiene wurden mit der Größenausschlußchromatographie (SEC) untersucht. Sie lassen sich mit Summen aus Schulz-Flory-Funktionen (SFF) beschreiben. Da eine Art aktiver Zentren eine SFF ergibt, die durch Molmassenmittelwerte definiert ist, lassen sich verschiedene Molmassenverteilungen nach Bandentrennung auf gleiche und verschiedene Arten aktiver Zentren untersuchen. In den untersuchten Systemen lassen sich zwei vergleichbare und eine unterscheidbare Art aktiver Zentren zuordnen. Auf diese Weise wurde das Kettenwachstum in Abhängigkeit von den Komponenten und Katalysatorformierungsbedingungen untersucht.
    Notes: Cis-1,4-polybutadiene was produced by polymerization of 1,3-butadiene using a catalyst system containing Ni(OOC8H15)2 and Al(C2H5)3 and the Lewis acids BF3 · O(C2H5)2 or TiCl4. The molar mass distributions (MMD) of the polybutadienes are investigated by means of size exclusion chromatography (SEC). The MMD's were fitted by a sum of Schulz-Flory-Functions (SFF). Taking into account that one kind of active species gives one SFF defined by molar mass averages, one comparable active species in both systems and one different were found. This way it was tried to find a relationship between the grown up of the active species depending on components and reactions conditions.
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    On the synthesis of acrylamide oligomers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 214 (1994), S. 115-122 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Synthese von Polyacrylamiden mit niedrigem Molekulargewicht (Mn = 500 - 1 000) durch metallaktivierte Polymerisation mit Wasserstoffperoxid in Wasser wird beschrieben. Von vier untersuchten Übergangsmetallsalzen erwiesen sich Cu2+ -Kationen als am effektivsten bei der Zersetzung von H2O2 und wurden deshalb als Aktivatoren verwendet. Die Versuche wurden bei drei Temperaturen (60, 80 und 95°C), drei verschiedenen H2O2-Konzentrationen (4, 5 und 6 Gew.-%, bezogen auf das Monomere) und vier unterschiedlichen Cu2+-Konzentrationen (900, 600, 300 und 0 ppm, Masse des Metalls bezogen auf das Monomere) durchgeführt. Dadurch konnten bei Monomerumsätzen über 95% Acrylamid-Oligomere mit Molekulargewichten im oben genannten Bereich erhalten werden. Innerhalb dieser Grenzen ist eine Molekulargewichtskontrolle nicht möglich, auch bei Verwendung verschiedener Cu2+-Konzentrationen. Die Grenzviskositäten sind ebenfalls sehr niedrig ([η] = 20 - 50 cm3/g), wobei zwischen diesen Werten und den Polymerisationsbedingungen keine Beziehung gefunden werden konnte. Die Ergebnisse ermöglichen die industrielle Herstellung von Acrylamid-Oligomeren.
    Notes: The synthesis of low-molecular-weight poly(acrylamide)s (M̄n = 500 - 1 000) is described. Metal-activated and non-activated polymerization in aqueous solution was investigated employing hydrogen peroxide as initiator. Among four transition metal salts considered, Cu2+ cations proved to be the most efficient in decomposing H2O2 molecules and were used as activator. The experiments were run at three reaction temperatures (60, 80 and 95°C), at three H2O2 levels (4, 5 and 6 wt.-% on monomer), and at four Cu2+ levels (900, 600, 300 and 0 ppm by weight of metal on monomer). Thus, ist was possible to prepare acrylamide oligomers with monomer conversions exceeding 95%, and with Mn values covering the narrow range indicated above. Within these low limits a molecular weight control is impossible, even with inclusion of the differentiated levels of Cu2+cations. Intrinsic viscosities are very low, too ([η]) = 20 - 50 cm3/g, without any relations of the individual values to variations of the given process parameters. The work provides an industrial route to very-low-molecular-weight acrylamide oligomers.
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    Aryl ether-ketone segmented polypyromellitimides (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 71-78 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Aromatische Ether-Keton-Sequenzen wurden in eine Polyimidkette eingebaut, um diesen die thermoplastischen Eigenschaften der Polyetherketone zu verleihen. Zu diesem Zweck wurden drei aromatische Diamine mit Ether- und Ketongruppen zwischen den aromatischen Ringen hergestellt und mit Pyromellitsäuredianhydrid kondensiert. Das thermische Verhalten von daraus hergestellten Polymerfilmen wurde untersucht.
    Notes: Aromatic ether-ketone segments have been incorporated into polyimide backbone to impart the well-known thermoplastic properties of polyether ketones. For this purpose three aromatic diamines containing ether and ketone connecting groups between aromatic rings have been prepared and polymerized with pyromellitic dianhydride to yield polyimides. The thermal behavior of the polyimide cast films has been investigated.
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    Antistatic modification of polyester with carboxyterminated poly(oxyethylene) (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 129-137 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Carboxy-terminierte Polyoxyethylene (PEO-acid) mit zahlenmittleren Molekulargewichten Mn = 8400, 3300 und 1000 wurden zur antielektrostatischen Modifizierung von Polyethylenterephthalat (PET) verwendet. Fasern aus PET-PEO-acid-Blends mit 2,0 oder 5,0 Gew.-% PEO-acid wurden bei 285°C mit einem normalen Extruder aus der Schmelze gesponnen und anschließend bei 80°C um das ca. 4,5fache verstreckt. Die Verarbeitbarkeit beim Verspinnen und Verstrecken war bei Verwendung von PEO-acid mit hohen Molekulargewichten ausgezeichnet. Die anti-elektrostatischen Eigenschaften wurden ebenfalls mit steigendem PEO-acid-Molekulargewicht besser. Da eine Umesterung beim Verspinnen nur in geringem Ausmaß stattfand, blieben die mechanischen Eigenschaften der Blend-Fasern gegenüber den PET-Fasern nahezu unverändert.
    Notes: Carboxy-terminated poly(oxyethylenes) (PEO-acid) with number-average molecular weights Mn = 8400, 3300, and 1000 were used for antielectrostatic modification of poly(ethylene terephthalate) (PET). The blend PET fibers containing 2.0 and 5.0 wt.-% of PEO-acids were melt-spun at 285°C with an ordinary extruder and then drawn about 4.5-fold at 80°C. The processabilities of spinning and drawing were excellent at higher molecular weights of PEO-acid. The anti-electrostatic properties of the blend fibers became also improved with increasing molecular weight of PEO-acid. Since little ester interchange reaction took place between PET and PEO-acid during meltspinning, the blend fibers could retain almost the same mechanical properties as the original PET fiber.
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    Preparation and characterization of spinning dopes for dry spinning of continuous alumina green fibers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 139-158 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Wäßrige Spinnmassen für das Trockenspinnen von Aluminiumoxid-Grünfasern wurden hergestellt. Dabei wurden basisches Aluminiumchlorid Al2(OH)5Cl · 2,5 H2O und SiO2-Sol als anorganische Komponenten und Polyvinylalkohol (PVA) als polymere organische Komponente eingesetzt.Bestimmte rheologische Eigenschaften der Mischungen sind essentiell, um eine gute Spinnbarkeit bei hohen Spinngeschwindigkeiten zu erhalten. Die Rheologie der Spinnmassen wird zum einen vom Molekulargewicht und dem Verseifungsgrad des PVA beeinflußt und zum anderen von der Zusammensetzung und der Konzentration der Mischung. Für Mischungen ohne SiO2 wurden die besten Ergebnisse bei einem PVA:Al2O3, Massenverhältnis von 18:82 und einem Oxidgehalt von ungefähr 27 Gew.-% erzielt. Der verwendete PVA hat ein mittleres Molekulargewicht von 70000 und einen Verseifungsgrad von 89%.Die Spinnmassen wurden mit Spinngeschwindigkeiten von bis zu 500 m/min zu kontinuierlichen Grünfasern versponnen. Die Struktur und das Alterungsverhalten von konzentrierten Lösungen von basischem Aluminiumchlorid wurden ausführlich untersucht.
    Notes: Aqueous spinning dopes for dry spinning of alumina green fibers were prepared by using basic aluminium chloride Al2(OH)5Cl · 2.5 H2O and SiO2 sol as inorganic components and poly(vinyl alcohol) (PVA) as polymeric organic component.Certain rheological properties of the mixtures are essential to achieve good spinnability at high spinning speeds. The rheology of the dope is influenced by the molecular weight and the degree of hydrolysis of the PVA, as well as by the composition and the concentration of the mixture. For mixtures without SiO2 best results were obtained at a PVA: Al2O3 mass ratio of 18:82 and an Oxide content of about 27 wt.-%. The PVA used has an average molecular weight of 70000 and a degree of hydrolysis of 89%.The dopes were spun to continuous green fibers at speeds up to 500 m/min. The structure and the ageing behaviour of concentrated solutions of basic aluminium chloride has been intensively studied.
    Additional Material: 10 Ill.
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    Interpenetrating polymer networks of polyurethane and furfuryl alcohol, IIa. Processability and properties of pultruded fiber-reinforced composites (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 41-52 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Herstellung von faserverstärkten interpenetrierenden Netzwerken (IPN) aus Polyurethan (PU) und Furfurylalkohol (FA) mittels Pultrusion wurde untersucht. Wie Viskositätsmessungen zeigen, nimmt die Topfzeit der PU/FA-IPN-Präpolymeren mit steigendem PU-Gehalt zu, und die Reaktivität ist hoch bei höheren Temperaturen. Aus morphologischen Untersuchungen geht hervor, daß mit steigendem PU-Gehalt die Benetzung der Fasern mit den PU/FA-Harzen verbessert wird. Die bei Zugversuchen erhaltenen Bruchflächen der glasfaserverstärkten PU/FA-IPNs mit PU-Gehalten unter 15 phr zeigen sogenannte “hackle patterns”. Die Zugfestigkeit der pultrudierten PU/FA-IPN-Composite ist bei einem PU-Gehalt von 5 phr am höchsten; Biegefestig-keit, Biegemodul und Wärmeformbeständigkeit nehmen jedoch mit zunehmendem PU-Gehalt ab. Die mechanischen Eigenschaften der mit Glas-, Carbon- oder Aramid- fasern (Kevlar 49) verstärkten pultrudierten Composite nahmen mit steigendem Volumenanteil der Fasern zu.
    Notes: A feasibility study of pultrusion of fiber-reinforced polyurethane/furfuryl alcohol (PU/FA) interpenetrating polymer/network IPN composites has been made. From the viscosity study, it was found that the pot life of the PU/FA IPN prepolymers increased with PU content and showed high reactivity at elevated temperature. It was confirmed from the morphological study that the wetting of fibers by the PU/FA IPN resins was improved with PU content. The appearance of the tensile failure surfaces of the pultruded glass fiber-reinforced PU/FA IPN composites showed “hackle patterns” for PU contents below 15 phr. The mechanical property study shows that the tensile strength of pultruded PU/FA IPN composites is the highest when the PU content is 5 phr. However, the flexural strength, flexural modulus and HDT decreased with PU content. The mechanical properties of various fiber-reinforced (glass, carbon, and Kevlar 49 aramid fiber) pultruded PU/FA IPN composites increased with fiber volume content.
    Additional Material: 8 Ill.
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    Determination of 1-butene distribution in LLDPE by DSC analysis after thermal fractionated crystallizationThis paper is dedicated to the memory of Dr. Umberto Zucchini, deceased on January 19, 1993. He was appreciated as a scientist in the Ziegler-Natta catalysis as well as a man of great humanity. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 219 (1994), S. 139-160 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Verteilung der Monomereinheiten (CCD) von LLDPE (1-Buten-Comonomer) wurde mittels thermischer Analyse untersucht. Nach der thermischen Behandlung der Polymeren durch thermisch fraktionierte Kristallisation (TFC) wurden die Schmelzendothermen in festgelegte Temperaturbereiche unterteilt. Die Verteilung der Endotherme gibt eine semiquantitative Aussage über die CCD.Beim Vergleich der thermischen Elutionsfraktionierung der gesamten Polymeren wie auch der einzelnen Fraktinen mit 13C-NMR-Messungen konnte eine gute Übereinstimmung festgestellt werden. Weiterhin wurde eine ungefähre Bestimmung der Ethylensequenzlänge durchgeführt.
    Notes: The chemical composition distribution (CCD) of LLDPE (1-butene comonomer) has been studied by thermal analysis. After an opportune thermal treatment of the polymers, thermal fractionated crystallization (TFC), the melting endotherms have been subdivided in areas with fixed temperature ranges. The distribution of the endotherms in different areas gave a semiquantitative idea of the CCD.The comparison with thermal rising elution fractionation and 13C NMR data of the whole polymers and fractions showed fairly good correlations. An approximate evaluation of the average ethylene sequence length was also obtained.
    Additional Material: 8 Ill.
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    Synthesis and biological activity of chlorine-containing polyketones (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 1-10 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Chlorhaltige Polyketone mit niedrigem Molekulargewicht wurden nach Friedel-Crafts aus Anisol, Chloracetylchlorid and Dichloralkanen (Dichlormethan, 1,2-Dichlorethan) in Kohlenstoffdisulfid hergestellt. Die Harze wurden mittels IR-Spektroskopie und Dampfdruckosmometrie charakterisiert. Das thermische Verhalten wurde thermogravimetrisch und differentialkalorimetrisch untersucht. Die Zersetzungscharakteristik wurde nach Broido und Doyle ermittelt. Die Prüfung der mikrobiellen Aktivität der Harze gegenüber Bakterien, Pilzen und Hefen ergab, daß sich die meisten Harze als Biozide verwenden lassen.
    Notes: Chlorine-containing polyketones of low molecular weight were synthesized from anisole, chloroacetyl chloride and dichloroalkanes, i. e. dichloromethane and 1,2-dichloroethane, by the Friedel-Crafts reaction using carbon disulfide as solvent. The resins were characterized by IR spectra and vapour pressure osmometry. The thermal properties were studied by thermogravimetry and differential scanning calorimetry. The characteristics of the decomposition reactions were evaluated by the Broido and Doyle methods. All the resins were tested for their microbial activity against bacteria, fungi and yeast. The results show that most of the resin can be used as biocides.
    Additional Material: 2 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052200101
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    Hydrolytic stability and mechanical properties of poly(ester urethanes) (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 49-60 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß der Hydrolysedauer bei 70°C auf die Molmasse und die mechanischen Eigenschaften handelsüblicher Polyesterurethane (Estane 54600, 54610 und 54650) wurde untersucht. Die Kinetik der Hydrolyse läßt sich als Reaktion erster Ordnung mit einer mittleren Induktionsperiode von etwa 7 Tagen beschreiben. Die resultierende Molmassenabnahme verursacht eine signifikante Verschlechterung der Eigenschaften, insbesondere der Bruchdehnung und der Zugarbeit bis zum Bruch, während die elastischen Eigenschaften weit weniger beeinträchtigt wurden. Eine quantitative Beziehung zwischen der relativen Änderung der Zugfestigkeit und der Molmasse wird vorgeschlagen. Die in der Reihenfolge 54650 〉 54600 〉 54610 abnehmende Hydrolysebeständigkeit der Estane läßt sich mit Unterschieden in deren chemischer Zusammensetzung erklären.
    Notes: The effect of hydrolysis time at 70°C on molar mass and mechanical properties of commercial poly(ester urethanes), i.e., Estanes 54600, 54610, and 54650, was analyzed. Kinetics of hydrolysis is plausibly described in terms of a first-order reaction with an average induction period of about 7 days. The resulting reduction of molar mass brought about a significant decrease in ultimate properties, particularly in stress at break and tensile energy to break, while elastic properties were affected much less. A quantitative correlation between relative changes in tensile strength and molar mass was attempted. Hydrolysis resistance of Estanes decreasing in the succession 54650 〉 54600 〉 54610 was related to their chemical composition.
    Additional Material: 7 Ill.
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    Effect of a curing accelerator on the glass transition temperature of non-stoichiometric epoxy amine networks (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 99-109 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Netzwerke aus Bisphenol-A-diglycidylether und 4,4′-Diaminodiphenylmethan wurden sowohl in Gegenwart unterschiedlicher Imidazolkonzentrationen als auch in Abwesenheit von Beschleunigern hergestellt. Dabei wurde das Verhältnis von Epoxidgruppen zu Aminwasserstoff variiert. Es wurde sowohl ein Überschuß an Aminwasserstoff als auch an Epoxidgruppen sowie ein stöchiometrisches Verhältnis von Epoxidgruppen zu Aminwasserstoff eingesetzt.Die Netzwerke wurden mittels thermomechanischer Analyse, Torsionspendelanalyse und uniaxialer Kompressionsmodulmessungen im Kautschukplateau untersucht. Weiterhin wurde eine Sol-Gel-Analyse der vernetzten Proben durchgeführt.Es wird gezeigt, daß Imidazol bei Einsatz eines Überschusses an Aminwasserstoff keinen signifikanten Einfluß auf die Glasübergangstemperatur und den löslichen Anteil der Proben hat. Im Falle eines stöchiometrischen Verhältnisses von Epoxidgruppen zu Aminwasserstoff oder eines Epoxidharzüberschusses hat Imidazol einen beachtlichen Einfluß auf die Glasübergangstemperatur der synthetisierten Netzwerke. Eine Abhängigkeit des löslichen Anteils der Proben von der Imidazolkonzentration konnte hauptsächlich bei Netzwerken festgestellt werden, die mit Epoxidüberschuß synthetisiert wurden.
    Notes: Networks were prepared from Bisphenol A diglycidylether and 4,4′-diaminodiphenylmethane both in the presence of different amounts of imidazole and in the absence of any accelerator. The ratio of epoxy groups to amino hydrogen was varied: the networks were made with amino hydrogen excess, a stoichiometric ratio of epoxy groups to amino hydrogen, and an epoxy excess.The resulting networks were investigated by thermomechanical analysis, by torsion pendulum analysis and by uniaxial compression modulus measurements in the rubbery-plateau zone. Further characterization was done by sol gel analysis of the cured samples.It was shown that imidazole does not significantly influence the glass transition temperature and the soluble content of the samples of an excess of amino hydrogen was used. In the case of a stoichiometric ratio of epoxy groups to amino hydrogen and in the case of an epoxy excess, imidazole considerably influences the glass transition temperature of the networks. A dependence of the soluble content of the samples on imidazole concentration used for network synthesis was found mainly in epoxy excess systems.
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    An example of free radical graft polymerization where the mechanism from-to applies (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 33-43 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Pfropfen natürlicher oder synthetischer Polymerer durch radikalische Polymerisation ist ein zur chemischen Modifizierung dieser Polymeren gebräuchliches Verfahren. Einige dieser chemischen Systeme zeigen bei genügend hohen Monomerkonzentrationen ein unerwartetes Ansteigen der Polymerisationsgeschwindigkeit, die in manchen Fällen auch wieder sinkt. Der Einfluß einer änderung der Monomerkonzentration auf die Pfropfausbeute bei der mit Cerionen initiierten Pfropfpolymerisation von Methylacrylat, Vinylacetat und einer Mischung beider Monomerer auf Cellulose wird diskutiert, wobei auf einen Drei-Komponenten-Pfropfmechanismus (“von”, “von-auf” und “auf”) Bezug genommen wird. Vermutlich wird das oben beschriebene Verhalten durch den Polymerisationsmechanismus “von-auf” verursacht. Daraus können Rückschlüsse auf die Copolymerstruktur gezogen werden.
    Notes: Free-radical grafting on natural and synthetic polymers is a method widely used to modify these polymers chemically. A number of these chemical systems show an unexpected behaviour of the polymerization rate when the monomer concentration is sufficiently high: it decreases and sometimes it increases afterwards. Here, the effect of varying the monomer concentration on the graft yield when grafting methyl acrylate, vinyl acetate and a mixture of both monomers onto cellulose initiated by ceric ions is discussed, considering a three-component mechanism of grafting (mechanisms from, onto and from-to). It is suggested that the unexpected behaviour indicated above is accounted for by the presence of the grafting mechanism from-to. Some knowledge about the copolymer structure can be reached by using this mechanistic approach.
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    Sulfobetaine polyurethane ionomers, 5. Tensile properties of polyether polyurethane ionomer and related compounds with Co2+ and Pb2+ (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 61-65 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Zug-Dehnungseigenschaften eines Polyetherpolyurethan-Ionomeren mit Sulfobetaingruppen wurden untersucht und mit denen des entsprechenden nichtionischen Polyurethans sowie davon abgeleiteten Compounds mit Pb2+ und Co2+ verglichen. Die Sulfonierung und die Behandlung mit Schwefelwasserstoff verbessern die Dehnungseigenschaften aufgrund der zunehmenden Phasensegregation bzw. der Bildung von Mikrophasen mit Halbleitereigenschaften durch Einschluß von Metallsulfiden. Die Komplexierung mit Pb2+ Co2+ verringert die Dehnungseigenschaften, bedingt durch teilweise Neutralisierung der ionischen Zentren.
    Notes: Stress-strain properties of sulfobetaine polyurethane ionomer based on polyether were studied comparatively to the non-ionic polyurethane and derived compounds with Pb2+ and Co2+. Sulfonation and treatment with H2S improve the tensile properties due to the increased phase segregation and to the semiconducting microphases formed by clustering of metal sulfides, respectively. Complexation with Pb2+ and Co2+ diminishes the tensile properties owing to the partial neutralization of ionic centers.
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    Electroinitiated polymerization of some new monomers with schiff's base structure and pyrrole moieties (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 103-115 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Monomere mit Pyrrol-Einheiten und dem Strukturelement der Schiffschen Basen wurden durch elektrochemische Oxidation bei gleichzeitiger Fällungspolymerisation in 1,2-Dichlorethan oder Acetonitril hergestellt. Als Monomere wurden Pyrrol-2-aldehydazin, N,N'-bis(2-pyrrolylmethylen)-1,4-diaminobenzol bzw. N,N'-bis(2-pyrrolylmethylen)-4,4′-diaminobiphenyl und als Elektrolyte Tetrabutylammoniumperchlorat, Tetrabutylammoniumtetrafluoroborat sowie Natrium-p-toluolsulfonat eingesetzt. Die dotierten Polymeren wurden mittels Elementaranalyse, IR-Spektroskopie und Thermoanalyse charakterisiert.
    Notes: Pyrrole-2-aldehyd azine, N,N'-bis(2-pyrrolylmethylene)-1,4-diaminobenzene and N,N'-bis(2-pyrrolylmethylene)-4,4′-diaminobiphenyl were polymerized by electro-chemical precipitating oxidation reaction in 1,2-dichloroethane and acetonitrile, respectively, in the presence of electrolytes like tetrabutylammonium perchlorate, tetrabutylammonium tetrafluoroborate and sodium p-toluene sulfonate. The doped resulted polymers were characterized by elemental analysis, IR spectroscopy and thermal analysis.
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    Characterization of thermoplastic poly(ethylene terephthalate)-glass fibre composites, 2Part 1 cf.7.. Mechanical behaviour (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 137-153 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß der Verarbeitungsbedingungen auf die Morphologie und die mechanischen Eigenschaften von unidirektionalen Composites aus Poly(ethylenterephthalat) und Glasfasern wurde untersucht. Im ersten Teil dieser Arbeit wurde über den Einfluß von Glasfasern auf die Kristallisationskinetik und die Matrixmorphologie von Poly(ethylenterephthalat)(PET) berichtet. Dabei wurden die Schmelz-und Kristallisa-tionsbedingungen, die thermische Stabilität und die Zugabe von Kristallisationskeimen (Talkum und Natriumbenzoat) berücksichtigt. Auf der Grundlage dieser Ergebnisse wurden mit Glasfasern gefüllte PET-Streifen unter verschiedenen Bedingungen zu Preßformplatten verarbeitet. Dynamische und statische Kurzzeit-Scherversuche sowie Langzeit-Biegefestigkeitsversuche wurden durchgeführt und unter Berücksichtigung der Verarbeitungsbedingungen und der Mikrophasenstruktur analysiert.
    Notes: The aim of this study was to understand how changes in processing conditions affect the morphology and ultimately mechanical performances of unidirectional poly(ethylene terephthalate) / glass fibre composites. In a previous paper, we have presented the influence of fibres on the crystallization kinetics and on the matrix morphology of poly(ethylene terephthalate) (PET), considering fusion-crystallization conditions, thermal stability and the addition of nucleating agents in the matrix (talc or sodium benzoate). Based on the results of that crystallization study, various processing conditions were implemented on compression-moulded plated made from PET-glass pultruded ribbons. Short-term (dynamic and static) shear tests and long-term flexural fatigue tests were performed to characterize the effects of moulding conditions. The mechanical results were analysed considering both processing conditions and microstructural parameters.
    Additional Material: 6 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052210112
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    Triazine-based polymers, 2. Synthesis and characterization of polyethers (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 187-205 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyether auf Triazinbasis können mittels phasentransferkatalysierter Polykondensation bei Raumtemperatur und Reaktionszeiten von 1 bis 3 h hergestellt werden. Von mehr als 20 Polyethern wurden Löslichkeiten, Glasübergangstemperaturen, thermogravimetrische Daten, Reißdehnungen, Reißfestigkeiten, Elastizitätsmoduli und Schlagzähigkeiten bestimmt. Von den Polymeren aus 2,4-Dichlor-6-diethylamino-s-triazin und Bisphenol A wurde zusätzlich der Kristallisationsgrad mittels Röntgenweitwinkelstreuung ermittelt. Das Inkrement des 1,3,5-Triazintriylrings wurde bestimmt, so daß die Glastemperaturen einiger Polyether nach van Krevelen berechnet werden konnten.
    Notes: Triazine-based polyethers can be synthesized by phase transfer catalysed interfacial polycondensation at room temperature and reaction times of about 1 to 3 h. In this way, more than 20 polyethers were synthesized and solubilities, glass transition temperatures, thermogravimetric data, elongations at break, tensil strengths, elasticity moduli and impact strengths were determined. In addition, the degree of crystallinity was investigated for the polymer obtained from of 2,4-dichloro-6-diethylamino-s-triazine and bisphenol A by wide angle X-ray diffraction. The increment of the 1,3,5-triazinetriyl ring was determined, which made it possible to calculate the glass transition temperatures of some polyethers according to van Krevelen.
    Additional Material: 1 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052210116
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    Synthesis of block copolymers by using polysilanes (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 207-216 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Methylmethacrylat wurde mit Poly(methylphenylsilan) als Photoinitiator polymerisiert. Durch Photolyse der in dem so hergestellten Polymethylmethacrylat (PMMA) noch enthaltenen Polysilanketten in Gegenwart von Vinylmonomeren wie Styrol wurden Blockcopolymere erhalten. Diese wurden eingesetzt, um Blockcopolymere mit Cyclohexenoxid herzustellen. Dies geschieht durch die Bildung von an PMMA gebundenen Silylradikalen, die in Gegenwart von N-Ethoxy-2-methylpyridinium-hexafluor-phosphat zu den entsprechenden Kationen oxidiert werden.
    Notes: Poly(methyl phenyl silane) was used to photoinitiate the polymerization of methyl methacrylate. Poly(methyl methacrylate) (PMMA), obtained this way, contains remaining polysilane chains. Photolysis of this PMMA in the presence of vinyl monomers such as styrene makes it possible to prepare block copolymers. Such PMMA prepolymers were also used to induce the polymerization of cyclohexene oxide through formation of PMMA-attached silyl radicals and subsequent oxidation to the corresponding ions in the presence of N-ethoxy-2-methylpyridinium hexafluorophosphate resulting in the formation of a block copolymer.
    Additional Material: 3 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052210117
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    Grafting of acrylonitrile onto bagasse dissolving pulp with KMnO4/oxalic acid systemPaper accepted for presentation at the 9th Arab Chemical Conference (Egyptian Chemical Society) from 10-13 April 1993 at the National Research Centre, Cairo, Egypt. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 25-30 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Chemiezellstoff wurde unter Verwendung eines KMnO4-Oxalsäure-Redoxinitiatorsystems mit Acrylnitril gepfropft. Der Einfluß von Monomer- und Initiatorkonzentration, Oxalsäurekonzentration, Reaktionszeit und -temperatur wurde untersucht.
    Notes: Bagasse dissolving pulp was grafted with acrylonitrile by using a KMnO4 oxalic acid redox initiator system. The effects of monomer concentration, reaction time, initiator concentration, acid concentration and reaction temperature were investigated.
    Additional Material: 5 Tab.
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    Effect of mixer rotor speed on interfacial crosslinking of epoxidized natural rubber and poly(acrylic acid) (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 31-48 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß der Mischerdrehzahl auf die Vernetzung von Polyacrylsäure (PAA) und epoxidiertem Naturkautschuk (ENR) wurde durch rheologische Untersuchungen (nach Monsanto), dynamisch-mechanische Analyse (DMA), Rasterelektronemikroskopie (SEM) und die Messung physikalischer Eigenschaften belegt. Hohe Mischerdrehzahlen verschlechtern demzufolge die Vernetzung von PAA und ENR. IR-Messungen deuten darauf hin, daß während des Mischens mit hohen Mischerdrehzahlen ENR-Elastomerketten mechanochemisch abgebaut werden.
    Notes: It is evident from Monsanto rheometric studies, dynamic mechanical analysis (DMA), physical property measurements and scanning electron microscopy (SEM) that the mixer rotor speed has an effect on the crosslinking of poly(acrylic acid) (PAA)/epoxidized natural rubber (ENR) blends. These studies reveal that mixing at high rotor speed deteriorates the crosslinking process between PAA and ENR. Infrared (IR) spectroscopic studies suggest that during mixing at high rotor speed ENR elastomer chains suffer breakdown through mechanochemical reactions.
    Additional Material: 12 Ill.
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    Synthesis of highly porous styrene-divinylbenzene copolymers prepared in the presence of 2,2,4-trimethylpentane (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 89-102 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Styrol-Divinylbenzol-(St-DVB-)Copolymere wurden in Gegenwart von 2,2,4-Trimethylpentan als Treibmittel hergestellt. Die Mengen an Verdünnungsmittel bzw. Vernetzer (DVB) wurden in den Grenzen 20-60 Vol.-% bzw.2-40 Vol.-% zur Bildung von verschiedenen Netzwerken variiert. Die charakterisitischen Eigenschaften der Netzwerke, wie Roh- und Reindichte, Porenvolumen, Porendurchmesser, Porendurchmesserverteilung und spezifische Oberfläche wurden durch Quecksilberporosimetrie bestimmt. Die Kompression, die am Anfang jeder Messung zu beobachten war, wurde bestimmt. Die Variation der Porenverteilung wurde anhand der Syntheseparameter diskutiert. Diese Resultate, in Verbindung mit den berechneten Porendurchmessern und mit Rasterelektronenmikroskop-Aufnahmen, zeigen, daß eine Mikrogel-Struktur vorliegt. Eine Überlappung des Netzwerkes tritt bei über 50 Vol.-% Verdünnungsmittel ein. Ein Makroporositätsbereich konnte bei Copolymeren mit spezifischer Oberflöche größer als 130 m2/g definiert werden.
    Notes: A large number of styrene-divinylbenzene copolymers (St-DVB) were synthesized using 2,2,4-trimethylpentane as pore-forming agent. Diluent and crosslinking agent (DVB) contents were varied in the ranges 20-60 vol.-% and 2-40 vol.-%, respectively, to generate various St-DVB networks. Network features as apparent and skeletal densities, pore volume, mean pore diameter, specific surface area and pore size distributions were measured by mercury porosimetry. A compressing process occurring at the beginning of each measurement has been revealed and measured. Depending on the two synthesis parameters, the changes in pore diameter distributions are discussed. Those results, combined with the calculated average pore diameter and microscopy observations, allow to conclude that the synthesized matrices have a microspheres-based structure with a network-overlapping process occurring over 50 vol-% of dilution. A macroporosity domain has been defined for networks having specific surface areas greater than 130 m2/g.
    Additional Material: 10 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052220107
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    Synthesis and characterization of N-alkylated polyamide-imides (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 103-109 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Neue aromatische Polyamidimide (PAI) wurden durch Reaktion von Torlon® 4203L (ein handelsübliches PAI) mit verschiedenen Halogenalkanen (Methyliodid, Ethyliodid, n-Butylbromid) hergestellt. Die Glastemperaturen dieser amorphen PAI liegen zwischen 238 und 276°C, die Grenzviskositäten betragen 51 bis 53 mL/g. Die PAI sind leicht löslich in polaren, aprotischen Lösungsmitteln wie z.B. N-Methylpyrrolidon, Dimethylformamid, Dimethylacetamid u.a. Der Einbau der Alkylsubstituenten in die Amidgruppen der PAI verbesserte die Verarbeitbarkeit aus der Schmelze, verringerte allerdings die thermischen Eigenschaften im Vergleich zu einem konventionellen PAI. Die bei 330°C und einer Frequenz von 0,1 rad/s gemessenen Schmelzviskositäten der hergestellten PAI betragen 103-105 Pa.s. Andererseits sind die Schmelzviskositäten der modifizierten PAI geringer als die von Torlon® 4203L, das mit dem konventionellen Polyetherimid Ultem-1000 vergleichbar ist.
    Notes: New aromatic polyamide-imides (PAI) containing various alkyl substituents were prepared by the substitution reaction of Torlon® 4203L (commercialized PAI resin) with the corresponding alkyl halides such as methyl iodide, ethyl iodide, and n-butyl bromide. The resulting amorphous PAIs with glass transition temperatures ranging from 238 to 276°C had inherent viscosities in the range of 51 to 53 mL/g. These polymers were readily soluble in aprotic polar solvents such as N-methylpyrrolidone, dimethylformamide, dimethyl acetamide, etc. Furthermore, the incorporation of various alkyl substituents into amide groups of the PAI resin increased the melt processability, but slightly decreased the thermal properties compared with conventional PAI resin. The melt viscosities of resulting PAIs determined at 330°C under the frequency of 10-1 rad/sec were in the range of 103-105 Pa.s. On the other hand, the modified PAIs showed significantly lower melt viscosities than Torlon® 4203L, which was almost comparable to the conventional polyetherimide, Ultem-1000.
    Additional Material: 3 Ill.
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    A biomaterial-based carbon fiber (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 147-163 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurde versucht, Sisalfasern zu kostengünstigen Kohlefasern zu carbonisieren. Vorbehandlung, Pyrolyse- und Carbonisierungsvorgang sowie Struktur und Eigenschaften der gebildeten Produkte wurden untersucht. Anwendungsmöglichkeiten für die aus Sisal hergestellten Kohlefasern mit mäßigen mechanischen Eigenschaften werden vorgeschlagen.
    Notes: An attempt to convert natural sisal fiber into low cost carbon fibrous materials was made. The pretreatment, pyrolysis and carbonization processes of raw sisal fiber as well as structure and properties of the resultant product were investigated. It was found that the sisal-based carbon fiber with moderate mechanical performance can be manufactured under the conditions applied. In addition, the application of the obtained sisal-based carbon fiber serving as functional material is presented.
    Additional Material: 12 Ill.
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    Deposition of hydrophobic layers onto acrylic fibers by plasma polymerization (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 189-200 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Abscheidungscharakteristik hydrophober Beschichtungen auf Acrylfaseroberflächen wurde untersucht. Der Einfluß von fluorhaltigen oder Siloxanmonomeren und der Variation der Plasmaeigenschaften wurde durch die Messung der Abscheidungsgeschwindigkeiten und der Wasser-Kontaktwinkel sowie der Untersuchung der chemischen Oberflächeneigenschaften ermittelt.
    Notes: Experiments aimed at the deposition of hydrophobic coatings on acrylic fiber surfaces are described. The effects of utilizing fluorine-containing and siloxane monomers and of varying plasma parameters have been assessed by measuring deposition rates, observing surface chemistry and determining water contact angels.
    Additional Material: 2 Ill.
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    Dendritische und “hyperbranched” PolymereVortrag anläßlich der Tagung der Fachgruppe “Makromolekulare Chemie” der Gesellschaft Deutscher Chemiker über “Fortschritte in der Polymersynthese” in Bad Nauheim, 21.-22. März 1994. Beispiele für die Beeinflussung von Polymereigenschaften durch gezielte Synthese von dreidimensionalen Strukturen (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 13-27 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dendritic polymers are highly branched structures with globular shape and high number of functionalities. In a divergent or convergent stepwise synthesis perfect macromolecules with controlled size and architecture are obtained. From the broad variety of dendrimer structures some examples are given and the properties of these unusual polymers are illustrated. For comparison the hyperbranched polymers, dendritic structures with defects made in a one-pot polycondensation reaction, are discussed. Differences and conformities of properties like molecular weight distributions, functionalities, solubility, viscosity behavior and glass transition temperatures for both globular polymer structures are explained.
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    Progress in synthesis and application of segmented polymersDedicated to Prof. Dr. H. Sinn on the occasion of his 65th birthday (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 47-60 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Maßgeschneiderte segmentierte Polymere spielen eine Schlüsselrolle bei der Entwicklung von neuen polymeren Materialien. In Abhängigkeit von den molekularen Architekturen der segmentierten Polymeren kann die Ausbildung von Polymermorphologien und von Eigenschaftssynergien gesteuertwerden. An ausgewählten Beispielen werden grundlegende Konzepte und neuere Entwicklungen vorgestellt. Segmentierte Silikon-Flüssigkautschuke, wo unverträgliche Silikonsegmente von zwei mischbaren Oligo(caprolacton)-Segmenten flankiert werden, sind wirkungsvolle Zähmodifikatoren für Epoxidharze. In nanophasenseparierten IPNs auf Basis dieser Silikon-modifizierter Epoxidharze kann die Schlagzähigkeit ohne Verlust der Dimensionsstabilität erhöht werden. Kompatibilisierte Blends aus segmentierten phenolischen Polyurethan- und epoxidfunktionellen Nitril-Flüssigkautschuken bilden diskrete Blend-Mikrophasen, die in Epoxidprepregs dispergiert sind und strukturelles Verkleben von Aluminium in Faser-Metall Laminaten ermöglichen. Reaktive Blendtechnologien werden entwickelt, um während der Polymerverarbeitung, z.B. von Polypropylen/Polyamid 6 Blends, in-situ Phasenvermittler herzustellen. Durch Einbau von definierten Oligo(tetrafluoroethene) Segmenten in Kodensationspolymere werden neben thermischen und mechanischen Eigenschaften auch Oberflächenspannungen und Gasdurchlässigkeiten variiert.
    Notes: Tailor-made segmented polymers play a key role in the development of novel polymeric materials exhibiting unsual bulk and surface properties. As a function of molecular architectures of segmented polymers, it is possible to control polymer morphologies and to achieve property synergisms. Selected examples are presented to illustrate basic concepts and recent developments. Segmented reactive liquid rubbers, containing an immiscible silicone segment flanked by two miscible oligo(caprolactone) segments, are efficient epoxy toughening agents. In such nano-phase-separated silicone-modified IPNs impact strength is improved without sacrificing dimensional stability. Compatibilized blends of segmented phenolic polyurethane and nitrile liquid rubbers produce rubber blend microphases dispersed in epoxy prepregs which are used to bond aluminum sheets in structural laminates. Reactive blending technologies are developed to produce segmented polymers as blend compatibilizers during melt processing, e.g., of polypropylene/polyamide 6 blends. Incorporation of oligo(tetrafluoroethene) segments into various condensation polymers modifies thermal and mechanical properties as well as surface tension and gas permeabilities.
    Additional Material: 13 Ill.
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    Olefinpolymerisation mittels metallocenkatalysatorenHerrn Prof. Dr.rer.nat., Dr.-Ing. E. h. Hansjörg Sinn mit den besten Wünschen zum 65. Geburtstag gewidmet (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 101-120 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Metallocenes have gained widespread interest as catalysts for olefin polymerization due to their high activity and versatility. A large range of new polymers with narrow molecular weight distribution and different microstructures can be produced with these “single-site” catalysts. These highly active catalysts which are able to produce 40 tonnes of polyethylene per gram zirconium per hour are even capable of incorporating remarkable amounts of sterically demanding olefins and dienes in copolymerization with ethylene. Isotactic, syndiotactic, stereoblock and isoblock polyolefins are accessible by variation of the metallocene ligands. Similarly, the isotacticity and molecular weight of the generated polyolefins are influenced by the ligand structure. By heterogenization of the metallocene on metal powder or silica polymers with substantially higher molecular weight, higher melting points and other new properties may be attained. Cyclic olefins like cyclopentene, norbornene or dimethanooctahydronaphthalene polymerize without ring-opening to yield highly melting and poorly soluble polymers. By separation of the racemic catalyst into enantiomers, optically active alkanes and alkenes are accessi-ble. Trimers are obtained with ee of 95%. These results provide new insights into the mechanism of Ziegler-Natta catalysis.
    Additional Material: 8 Ill.
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    Propylene polymerization with metallocene catalysts in industrial processesDedicated to Prof. Dr. Dr. Ing. E. h. Hansjörg Sinn on the occasion of his 65th birthday (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 155-164 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Product demands for polypropylene polymers cover a wide range of properties. Metallocene catalysts open up the way to influence the molecular properties of polypropylene by altering the ligand system of the metallocene complexes. This leads to new products with application properties which are not available with conventional catalysts. Concepts are presented to adapt metallocenes to modern, industrial polymerization processes. Some examples illustrate the particular advantages of this new generation of catalysts.
    Additional Material: 6 Ill.
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    Hochmolekulare lösliche polymere mit coronandenstruktur-synthese und eigenschaften (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 223 (1994), S. 193-201 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New polymers with an alternating sequence of aliphatic chains and coronands were synthesized via Diels-Alder addition polymerization of bis(2-pyrones) with bismaleimides. The chemical structures of these polymers 6 are supported by NMR spectra, model reactions and crystal X-ray structure analysis. The tetrafunctional maleimide 5 was synthesized and the cyclization of 5 to the bicycle 9 with 2 mol monopyrone 8 was carried out.
    Additional Material: 3 Ill.
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    The biodegradation of polymers: Recent resultsPaper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 21-35 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: After a general introduction including definition of biodegradability, the recent literature is briefly summarized. The results obtained in our laboratory for various polymers in three different composting units are then presented. They demonstrate that there is an urgent need for a quantitative method to characterize polymer biodegradation. For that purpose, a manometric method which allows the measurement of the oxygen consumed by the growing microorganisms has been developed. It has been tested with various inocula of increasing complexity: one Streptomyces sp., a mixture of three Streptomyces (badius, setonii and viridosporus), a compost extract or sewer sludge, growing in the presence of low molecular weight molecules as sole carbon source. Its performances and limitations are discussed. It is then applied to various polymer systems: polyesters and their constituent units, autoxidized polyethylene (APE) and its model compounds, polyvinyl alcohol (PVAl), starch and cellulose. The biodegradability of these polymers is characterized and their potential use as biodegradable materials for packaging, sanitary and agricultural uses is discussed.
    Additional Material: 9 Ill.
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    Cetylpyridinium chloride-modified poly(ethyleneimine) for the removal and separation of inorganic ions in aqueous solution (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 215 (1994), S. 175-188 
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    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Entfernung und Trennung einer Reihe von Metallionen mit Hilfe des wasserläoslichen Cetylpyridiniumchlorid-modifizierten Poly(ethylenimin)s (PEI-CPC) wurden in Kombination mit der Membranfiltration untersucht. Die Liquid-Phase Polymer-Based Retention(LPR)-Methode wurde zur Abtrennung von niedermolekularen Spezies beiverschiedenen pH-Werten und bei mehreren Elementkonzentrationen herangezogen. Die Studie umfaßt wäassrige Läosungen der Anionen Chromat und Phosphat sowie der Kationen Cu(II), Zn(II), Co(II), Ni(II), Cr(III), Fe(III), Cd(II), Pb(II) und Sr(II). Die Ergebnisse zeigen, daß eine hohe Retention für beide Anionen und auch für die meisten untersuchten Metallionen erzielt wurde. PEI-CPC zeigte gute Abtrenneigenschaften für Chromat-und Phosphationen selbst bei relativ hohen Anionenkonzentrationen 85 bzw. 150 mg · L-1und ebenso fäu die meisten untersuchten Metallionen. Im Falle der Cu(II)-, Ni(II)-und Sr(II)-Lonen wurde eine selektive Interaktion beobachtet. Das Polymerreagenz und seine Interaktionsprodukte wurden durch IR- und UV/Vis-Spektrometrie sowie Viskosimetrie charakterisiert. Zusäatzlich wurde das Interaktionsverhalten durch die Retentionsfäahigkeit untersucht. Eine gute Korrelation wurde zwischen den Retentionsdaten und den IR-und UV/VIS-Spektren der Interaktionsprodukte des Polymerreagenzes mit den Metallionen gefunden.
    Notes: The removal and separation of a series of ions by the water-soluble cetylpyridinium chloride-modified poly(ethyleneimine) (PEI-CPC) in conjunction with membrane filtration were investigated. The Liquid-Phase Polymer-Based Retention (LPR) method was applied to study the removal of the low-molecular species at different pH values and at several element concentrations. The study comprises aqueous solutions of the anions chromate and phosphate, and of the cations Cu(II), Zn(II), Co(II), Ni(II), Cr(III), Fe(III), Cd(II), Pb(II) and Sr(II). The results show that a high retention was attained in neutral solutions for both anions and also for most metal ions investigated. PEI-CPC exhibited good removing abilities for chromate and phosphate ions even at relatively high concentrations of anions (85 and 150 mg · L -1, respectively) and also for most of the metal ions studied. In the case of Cu(II), Ni(II), Cd(II), and Sr(II) ions, selective interactions were observed. The polymer reagent and its interaction products were characterized by IR, UV/VIS spectrometry, and viscometry. In addition, the interaction behaviour was investigated by the retention ability. A good correlation was found between the retention data and the IR and UV/VIS spectra of the interaction products of the polymer reagent with the metal ions.
    Additional Material: 7 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052150115
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    Reaction of hals in polypropylene during light exposure: Part 1-iso-octane as reaction model compound -Paper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 101-112 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photo and thermal reactivity of nitroxyl radicals derived from di-, (oligo)meric hindered amine light stabilizers (HALS) on iso-octane, a model compound for polyprophylene, was studied and compared to that of monomeric 2,2,6,6-tetramethyl- piperi-dine-N-oxyl (TEMPO).The exchange-interaction among 〉N—O. groups seems to affect only the thermal process.
    Additional Material: 3 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052160107
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    Application of chemiluminescence to polymer degradation studies. Thermal oxidation of polyamide 6.Paper presented at the “15th Annual International Conference on Advances in the Stabilization and Degradation of Polymers” in Luzern (Switzerland), June 2-4, 1993. (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 216 (1994), S. 169-186 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chemiluminescence (CL) technique was used to study the thermal oxidation of polyamide 6 samples with different ratio of terminal basic and acid groups, which perform a distinct effect on kinetics of the isothermal CL - time runs at 120-140°C. The isothermal experiments are complemented by nonisothermal ramp experiments where the CL intensity is monitored against temperature at a programmed rate of temperature increase.The relation of parameters such as initial CL intensity, integrated value of CL intensity for both isothermal and nonisothermal experiments and rate constants corresponding to CL - time curves was discussed within the results of other oxidation stability tests as absroption of oxygen, thermogravimetry, etc.
    Additional Material: 11 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052160112
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    Modified styrene-isoprene-styrene block copolymer membranes complexed with cobalt-containing schiff's bases for oxygen permeation (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 31-41 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die strahleninduzierte Pfropfpolymerisation von 4-Vinylpyridin (VP) und 1 -Vinylimidazol (VIm) auf ein Styrol-Isopren-StyroI-Blockcopolymeres (SIS) sowie die Gasdurchlässigkeit von daraus hergestellten Membranen wurde untersucht. Eine Komplexierung der modifizierten SIS-Copolymeren (SIS-g-VP bzw. SIS-g-VIm) mit Cobalt enthaltenden Schiffschen Basen (CoS) als fixierte Sauerstoffträger verbesserte deren Sauerstoffdurchlässigkeit. Der Mechanismus des Sauerstofftransports wird diskutiert.
    Notes: The grafting of 4-vinylpyridine (VP) and 1-vinylimidazole (VIm) onto styrene-isoprene-styrene (SIS) triblock copolymer by radiation-induced graft copolymerization was studied. The effect of grafting degree on gas permeability of membranes made of grafted copolymers was investigated. The complex formation of the modified SIS (SIS-g-VP or SIS-g-VIm) with cobalt-containing Schiff's bases (CoS) in chloroform solution was studied. Facilitated transport of molecular oxygen in modified SIS membranes containing CoS as fixed carrier of oxygen, and oxygen permeability in modified SIS membranes due to the oxygen binding ability to CoS was observed. Mechanism of oxygen transport across the SIS-g-VP-CoS and SIS-g-VIm-CoS membrane is discussed.
    Additional Material: 5 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052170104
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    Electron beam initiated grafting of methyl methacrylate onto polyethylene: Structure and properties (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 61-69 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyethylen (PE, 100 Gew.-Teile) wurde mit Methylmethacrylat (MMA, bis zu 5 Gew.-Teilen) gemischt und anschließend mit Elektronen (bis zu 20 Mrad) bestrahlt, um PE/MMA-Pfropfcopolymere herzustellen, deren Bildung mittels IR-Spektroskopie nachgewiesen wurde. Gelbildung wies auf eine Vernetzung während der Bestrahlung hin. Zunehmende MMA-Konzentration und höhere Bestrahlungsdosen verringerten die Kristallit-Schmelztemperatur und den Kristallisationsgrad des PE. Zugfestigkeit, Bruchdehnung und Dielektrizitätskonstante wurden gemessen und diskutiert.
    Notes: Polyethylene (PE, 100 parts by weight) was mixed with methyl methacrylate (MMA, up to 5 parts by weight) at 120°C and subsequently exposed to electron radiation of different doses (up to 20 Mrad) to prepare PE/MMA graft copolymers. Successful grafting was verified by IR spectroscopy. Gel formation indicated crosslinking. Grafting increased with increasing MMA concentration and increasing irradiation dose. Crystalline melting temperature and percent crystallinity were lower than those of untreated PE. Tensile strength, elongation at break and dielectric constant of grafted samples were measured and discussed.
    Additional Material: 7 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052170107
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    Reactive blending of thermosets: Molecular, morphological and mechanical analysis (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 159-190 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Mit einer Reihe unterschiedlicher Methoden wurde versucht, die Zähigkeit tri- und tetrafunktioneller Epoxid- sowie ungesättigter Polyesterharze zu erhöhen. Die Epoxidharze wurden durch harte, thermisch stabile Konstruktionskunststoffe, ein Bisphenol-A Polycarbonat bzw. ein thermoplastisches Polyetherimid (Ultem 1000), modifiziert. Bei den ungesättigten Polyesterharzen wurde ein anderes Verfahren angewendet: Zwei handelsübliche flüssige Kautschuke wurden chemisch modifiziert, um ihre Reaktivität gegenüber den funktionellen Gruppen der Matrix zu steigern: Ein hydroxyterminiertes Polybutadien und ein aminoterminiertes Butadien-Acrylnitril-Copolymeres wurden zu Polymeren mit Isocyanat- bzw. Maleimidendgruppen umgesetzt. Ein weiteres hier beschriebenes System zielt darauf ab, die rasch abnehmende Steifheit der Polyestermatrix bei Temperaturen oberhalb Raumtemperatur zu verringern. Dazu wurde ein hitzehärtbares Bismaleimidharz als zweite co-reaktive Komponente in den Polyester eingebracht.
    Notes: A number of different approaches were used to enhance the toughness of tri- and tetrafunctional epoxies and of unsaturated polyester resins. In the case of epoxies, tough, thermally stable, engineering thermoplastics, namely a bisphenol-A polycarbonate and a thermoplastic poly(ether imide) (Ultem 1000) were employed as modifiers. For unsaturated polyesters a different approach was adopted: two commercial liquid rubbers were chemically modified to enhance their reactivity towards the matrix functionalities. In particular, a hydroxy-terminated polybutadiene and an aminoterminated butadiene-acrylonitrile copolymer were transformed into isocyanate-terminated and maleimide-terminated rubbers, respectively. A further system which is described in the present contribution is aimed at mitigating another deficiency of the polyester matrix, namely its rapidly decreasing rigidity at temperatures above room temperature. In this case, a thermosetting bismaleimide was incorporated into the resin as a co-reactive second component.
    Additional Material: 28 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052170115
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    Recycling of egyptian bagasse pith wastes in the synthesis of cationic resins (1994)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 1-10 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Eine Reihe sulfonierter kationischer m-Kresol-Paraformaldehyd-Harze wurden aus dem Mark ägyptischer Bagasse hergestellt. Reaktionsbedingungen werden angegeben, und die Eigenschaften der hergestellten Bagassemark/m-Kresol/Formaldehyd-Harze werden mit denen von Harzen ohne Bagassemark verglichen. Die synthetisierten Polymere sind stabil in Wasser, verdünnten Mineralsäuren (1 M) und organischen Lösungsmitteln sowie gegenüber thermischer Behandlung. Die Harze besitzen Kationenaustauscherkapazitäten von bis zu 2,91 meq/g (bezogen auf trockenes Harz) und werden als Austauschermaterialien für eine mögliche Trennung zweiwertiger Kationen getestet.
    Notes: A series of sulfonated cationic resins have been prepared and characterized from Egyptian bagasse pith wastes (as a source of cheaper and renewable material) with m-cresol and paraformaldehyde as a crosslinking agent. Reaction conditions for the preparation are presented and properties of the synthesized sulfonated bagasse pith-m-cresol-formaldehyde resins are described and compared with resin not containing bagasse pith. The synthesized resins are stable in water, dilute mineral acids (1 M), organic solvents, and to thermal treatment. The resins having a cation exchange capacity up to 2.91 meq g-1 of dry resin, are being introduced as new exchangers. The synthesized resins are used in the study of the possible separation of some bivalent cations.
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/apmc.1994.052180101
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    Polyspirodilactam: A new family of high temperature polymers (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 6-11 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A new class of materials based on a spirodilactam structure has been recently synthesized as part of research into new polymeric materials. Not only is the spirodilactam structure novel, but it was not even the intended product in the synthesis as originally designed. The polymerization process discovered by the reaction of 4-ketopimelic acid or its corresponding spirodilactone with primary amines opened a new field of polysprodilactam chemistry. This paper describes the chemistry leading to the discovery of spirodilactam-based polymers and initial applications in the area of thermoplastics and thermosets. Most recent developments to be covered include aromatic spirodilactams and isomeric spirodilactams.
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    High temperature thermosets based on the cocuring of a novel spirodilactam bisallylether and bismaleimide (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 12-16 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Spirodilactam bisallylether is a new high temperature performance monomer. It melts at 154°C, and is thermally inactive in forming a homopolymer. However, it reacts readily with a bismaleimide via “ene” reaction. Therefore, it could be used as a comonomer and an effective toughening modifier for bismaleimide. The properties of the blends of spirodilactam bisallylether and 4,4'-bismaleimidodiphenyl-methane were studied. The cocured resins have high glass transition temperature, 〉 300°C. By adding 30 to 40 mole % of the bisallylether, the compact tension toughness of the bismaleimide was improved to 0.7 MPa-m1/2. Therefore, the resins have a combination of high glass transition temperature and toughness. They also showed good flexural properties. Despite the high water absorption, 5 to 7%, the resins retained high hot/wet flexural properties because of the high glass transition.
    Additional Material: 3 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340106
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    Compatibilization of immiscible blends with a mutually miscible third polymer (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 59-68 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Four immiscible blend systems, styrene-maleic anhydride/styrene-acrylonitrile (SMA/SAN). styrene-maleic anhydride/acrylonitrile-butadiene-styrene (SMA/ABS), poly(vinylidene fluoride)/SAN (PVF2/SAN), and PVF2/ABS, were investigated. The effect of adding up to about 10 wt% of a third polymer that is miscible with each blend component, poly(methylmethacrylate) (PMMA), was determined. In every case, the addition of PMMA led to the improvement of properties such as tensile strength, tensile elongation, and notched impact strength. Furthermore, the addition of PMMA resulted in finer, more uniform dispersions of the primary blend components. The experimental results are interpreted in terms of interfacial activity of the common phase component, PMMA.
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    A thermoanalytical study on solid-state cure of poly(p-phenylene sulfide) (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 81-85 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Differential scanning calorimetry (DSC) was used to investigate the solid-state cure process of poly(phenylene sulfide)(PPS) resin. Virgin PPS resin in an open sample pan was cured in DSC cell. Either air or oxygen was used as a curing atmosphere. Cure temperatures were in the range of 200 and 250 °C, which are below the melting point of PPS resin. Cure temperature as well as atmospheric condition influenced the cure behavior of PPS in the solid state. Both the rate and the amount of cure increased with increasing cure temperature. On the other hand, the time to reach the maximum cure rate was independent of cure temperature. Changing the atmosphere from air to oxygen increased both the cure rate and the amount of cure. The size effect of PPS particles on the cure reaction was also discussed.
    Additional Material: 9 Ill.
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    The anisotropy of slow crack growth in polyethylene pipes (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 109-115 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Slow crack growth was measured in the perpendicular and parallel directions relative to the extrusion direction of the pipe. For five pipes from different manufacturers, the anisotropy factor, the lifetime to fracture in the perpendicular direction divided by lifetime in the parallel direction, varied from 1.2 to 4.7 for complete fracture and 1.4 to 4.0 for crack initiation. The degree of molecular orientation was determined by measuring the shrinkage that occured when a pipe specimen was heated near its melting point. The amount of shrinkage correlated with the anisotropy factor for slow crack growth. The shape change after shrinkage was related to the flow pattern of the resin during extrusion and the cooling rate after extrusion.
    Additional Material: 9 Ill.
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    Viscoelasticity of some engineering plastics analyzed with the modified stress-optical rulePart 7 of the series “Birefringence of Amorphous Polymers.” (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 135-140 
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    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The complex Young's modulus, E*(ω), and the complex strain-optical coefficient, O*(ω), of poly(ether sulfone) (PES), polysulfone (PSF), and polyethermide (PEI), were measured over the frequency range 1 to 130 Hz. The data were analyzed with a modified stress-optical rule: The Young's modulus was decomposed into two complex functions, EG*(ω) and ER*(ω); the modified stress-optical coefficient, CR and CG, associated with the rubber (R) and glass (G) components, respectively, were determined. The results for six polymers, including polystyrene, poly(α-methyl styrene), and bisphenol A polycarbonate were compared with each other. One of the coefficients, CR, equivalent to the stress-optical coefficient in melts, mainly depended on the way in which phenyl groups were connected to the chain. The other, CG, was in the range of 20 to 40 Brewsters, and did not strongly depend on the details of polymer structure. The component function, EG*(ω), which was located in the glassy region and originated from the high glassy modulus, was almost the same in shape when plotted against ω with double logarithmic scales. The R component, ER*(ω), located at the long time end of the glass-to-rubber transition zone, was slightly sensitive to the molecular structure of polymers.
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    A closer look at the MWD-viscosity transform (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 159-165 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: While there is abundant evidence that the molecular weight distribution (MWD) of a linear polymer has an influence on the shape of the viscosity function, the ability to convert the viscosity function to an MWD has been questioned. Using strictly numerical techniques, we have shown that the viscosity function can be transformed to the MWD, but always with some distortion. However, distinct bimodality can be qualitatively preserved through both the MWD-viscosity and viscocity-MWD transforms.
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    A model for the unfoamed skin on microcellular foams (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 169-173 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In microcellular plastics, an unfoamed skin that is integral with the foamed core can be created by allowing the nucleating gas to diffuse from the surfaces of a gas saturated specimen prior to foaming. In this paper, a semi-empirical model is proposed that predicts the skin thickness variation in microcellular foams as a function of gas desorption time. The model shows good agreement with experimental results on the polycarbonate-carbon dioxide system.
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    URL: http://dx.doi.org/10.1002/pen.760340302
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    Kinematics and deformation characteristics as a mixing measure in the screw extrusion process (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 174-189 
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    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The present paper proposes “Deformation Characteristics” (DC) as a new deformation measure of screw extrusion processes, based on the Green deformation tensor. In contrast to previous strain measures heuristically proposed by Mohr, et al., Mckelvey, and Pinto and Tadmor, the new DC can naturally incorporate the demixing phenomena and systematically take into account the three-dimensional circulatory flow with the screw flight effect. Therefore, DC can be regarded as an improved strain measure. “Weighted Average Deformation characteristics” (WADC) is also proposed to indicate the overall deformation characteristics as a quantitative measure to the “goodness of mixing” of the extrusion process. The present paper includes discussion on delicate differences between DC and several other strain measures in case of the two-dimensional velocity approximation, and on the application of DC into a general three-dimensional velocity field obtained by a quasi-three-dimensional finite element analysis of extrusion processes. In determining WADC in the three-dimensional application, the residence time distribution function, including the three-dimensional circulatory flow effect, is used.
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    Simulation of non-isothermal flow in modular co-rotating twin screw extrusion (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 229-237 
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    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Non-isothermal flow is simulated in the screw and kneading disc elements in a modular co-rotating twin screw extruder. Methods of calculating mean temperature rises for individual elements are discussed and results are presented. The implications of non-isothermal operation for scale-up is discussed. A method is then described for making calculations in a modular co-rotating machine, that contains many different elements. Example calculations are given showing the tendency of larger machines to buildup greater temperatures when viscous heating is included.
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    URL: http://dx.doi.org/10.1002/pen.760340309
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    Influence of a compatibilizing agent on the phase morphology of a polyethylene-polyamide 6 blend in a modular intermeshing co-rotating twin screw extruder (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 221-228 
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    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study of the influence of a compatibilizing agent on phase morphology development in a 75/25 polyethylene/polyamide-6 blend in a modular co-rotating twin screw extruder is presented. The development of phase morphology along the axis of the modular screw was observed by cooling the extruder and removing the polymer from the screw channels. Changes in phase morphology due to the addition of a compatibilizer have been investigated using scanning electron microscopy. Sufficient quantities of compatibilizing agent produce significant increases in the rate of mixing and also reduce the scale of the phase morphology. Much larger quantities (5%) than actually required for interface coverage are needed for rapid mixing. This seems to be due to the high viscosity of the matrix.
    Additional Material: 10 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340308
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    Publications by P. H. Lindenmeyer (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 251-251 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340403
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    Masthead (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994) 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340401
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  • 88
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    Does quantum magic impinge on polymer physics? (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 260-265 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Penrose states that quantum effects can occur even in relatively large systems when energy differences remain small. This is just the situation with polymer materials. A quantum description by Penrose of the formation of quasi-crystals can be rewritten to apply to polymer crystallization. The implications of the need to take account of quantum effects are discussed. Another approach based on the quantization of energy levels in clusters of atoms offers a possible explanation of heat setting in nylon and polyester fibers. Finally some problems of the interpretation of quantum theory are discussed.
    Additional Material: 1 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340405
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    A novel approach to a truly dynamic thermodynamicsEditor's note: Paul Lindenmeyer remained active in his retirement and left a legacy of several manuscripts in various stages of completion. We have selected one of his manuscripts as a contribution to this memorial issue. This paper presents some of the controversial issues of nonequilibrium thermodynamics that Paul was attempting to address. Professor Astarita kindly agreed to provide comments and a critique regarding the approach and ideas advocated by Paul Lindenmeyer. (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 252-259 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A novel approach to a truly dynamic thermodynamics is proposed in which equilibrium is defined in terms of explicit time, distance, and acceptable error scales. This approach involves reformulating the second law of thermodynamics in terms of an excess energy that vanishes at equilibrium instead of an entropy that assumes some unknown maximum value. Excess energy is defined mathematically as the total Legendre transform of energy with respect to an independent set of extensive variables. Excess energy is effectively the free energy functional of a nonequilibrium system and is a function of the time, distance, and acceptable error scales. Elimination of entropy from thermodynamics requires recognizing temperature as a thermal stress, proportional to the antimetric component of the stress tensor that is neglected when one assumes the validity of Cauchy's second law of motion. The inclusion of temperature as part of the stress-strain couple completes the science of thermomechanics and opens the way for a practical unification of chemistry and physics in strictly mechanical terms.The last sentence of the abstract shows how high the goals that Lindem meyer set for himself were. I personally do not agree with the idea that mechanics is the queen of all sciences, and that given deep enough probing one could achieve “a practical unification of chemistxy and physics in strictly mechanical terms”; for instance, electromagnetism has full citizenship's rights in physics, and it is hard to conceive that it could be reduced to mechanics.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340404
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    Characterization of the interfacial bond in paper-polypropylene-paper laminatesDedicated to the memory of Paul H. Lindenmeyer, colleague and friend. (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 285-289 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The interfacial strength of two paper-polypropylene-paper laminates used for electrical power transmission cable insulation has been measured using a peel test after a variety of conditionings that simulate the service thermal stress conditions. Immersion in dielectric oil at 23°C causes little decrease in peel strength, but heating in the oil at 90°C causes a rapid initial loss followed by a slow loss of strength. Cyclic and static heating show that cyclic fatigue is not a factor as the initial loss of strength occurs in a time comparable to the first two test cycles and further heating causes much less loss of strength. Tensile and compressive stresses resulting from cable winding have no effect on the loss of bond strength during heating in oil. Vacuum drying of the laminate and oil (as in cable manufacture) before heating results in less decrease in peel strength than heating without prior drying. Optical and electron microscopy show minimal wetting of the paper fibrils by the polypropylene with only a few having been either normal to or at a steep angle to the polypropylene surface. That is, the fibrils appear to be parallel to the interface and only partially immersed in the polypropylene. Micrographs show little, if any, differences between the interfaces on the two sides as well as little paper on the polypropylene after delamination and vice versa. It is suggested that the bonding mechanism is a combination of weak mechanical interlocking and secondary bonds. It is also suggested that swelling of the polypropylene relative to the paper by the dielectric oil at 90°C weakens the interfacial bond.
    Additional Material: 7 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340409
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    The effect of annealing on stretched trans-1,4-polyisoprene networks (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 290-300 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Variations of stress with temperature for stretched networks of trans-polyisoprene networks in the crystallization region are reported. Such profiles are characteristically U-shaped with the stress at lower temperatures often climbing to high levels. Valley widths of the profiles narrow as annealing temperature increases to about 50°C, then widen at yet higher temperatures. The degree of crystallization at 22°C is 37% and independent of deformation and annealing temperature. The β crystal form is overwhelmingly present with traces of other crystal forms appearing only at high deformations. The theory of stress-induced crystallization provides a good description of experimental results provided the nucleation parameter σ is dependent upon deformation. Therefore, the data provide good qualitative support for the theory in its current form.
    Additional Material: 15 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340410
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    Thermoplastic polyheterocycles. I: Polyalkylene-benzoxazolesPresented in part at the 25th anniversary meeting of the ACS Polymer Group of the North Carolina Section of the American Chemical Society, Chapel Hill, N.C., Nov. 12, 1992. (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 301-304 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polyalkylenebenzoxazoles of high molecular weight (inherent viscosity values from 0.76 to 2.95) were prepared from 4,6-diaminoresorcinol dihydrochloride and aliphatic diacids in polyphosphoric acid by heating at 180 to 200°C for 3-5 h. Melting points of the polymers ranged from 148 to 423°C, depending on the length of the alkylene chain. Glass transition temperatures were relatively low, ranging from 50 to 100°C and did not show the pronounced odd/even effect noted for melting points. In all cases, rapid weight loss occurred above 400°C. No evidence for the formation of a molecular composite was observed in an attempt to prepare in situ a rod-like polybenzoxazole in a polyalkylenebenzoxazole.
    Additional Material: 2 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340411
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    Masthead (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994) 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340201
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    Oligomer distribution for interfacial step growth polycondensation (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 93-101 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Low levels of oligomer molecules are generally desirable in polymeric materials. It is known that several reactor variables can affect the oligomer distribution, and therefore it is useful to have predictive models for molecular weight distribution. The normal approach of a differential equation-based model is very complex to set up if it is applied rigorously to include all the non-Flory aspects of the step growth polycondensation and in particular the interfacial polycarbonate polymerization. In this paper, simple methods based on the Monte Carlo method and Stockmayer distribution are applied to simulate the effects of mass-transfer, unequal reactivity, and the starting stoichiometry of the polycondensing functional groups on the oligomer distribution. It is shown that these parameters can have a significant effect on the oligomer weight distribution and polydispersity of the final polymer.
    Additional Material: 4 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340204
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    Mechanical properties and deformation mechanism of polyoxymethylene chain in the crystalline state (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 308-317 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The true crystallite modulus of polyoxymethylene (POM) was evaluated experimentally and thoeretically as a function of temperature. The mechanical deformation mechanism of POM was lattice-dynamically predicted and confirmed by measuring the stress-induced vibrational frequency shifts of the infrared and Raman spectra, which were interpreted on the basis of anharmonic potential field.
    Additional Material: 11 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340413
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    Analysis of the temperature rise in the projectile and extended chain polyethylene fiber composite armor during ballistic impact and penetration (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 141-152 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The ultra-high strength/modulus, extended chain polyethylene fiber (Spectra® fiber) composite has shown great potential as a lightweight armor material with its extraordinary capability of absorbing the kinetic energy of projectiles. But the relatively low melting point of this fiber (∼ 145°C) has caused concerns regarding the effect of temperature rise during the impact/penetration process on the performance as armor material. In this article, an analysis of temperature rise in projectile and the fiber composite during the impact/penetration process is described. Combining the simulation of impact deformation by finite element analysis and the simulation of temperature rise by a finite difference approximation of the related dynamic equations, the temperature rise caused by the projectile/composite interaction was estimated. Results show that there is a significant temperature rise at the projectile/composite interface due to the friction but that the short length of time involved in the process and the low thermal conductivity of Spectra fiber composite keep the temperature rise in a very small region (in the order of 0.001 cm) around the interface during the impact/penetration process. Consequently, the volume that is affected by the temperature rise is very small, in the order of total 0.001 cm3 around the projectile, and this is too small to generate any detectable effect on the armor performance. After the projectile is stopped, however, substantial heating of fiber composite can occur under specific conditions as the result of heat flow from the hot projectile embedded in the composite. This heating of fibers, however, is a postmortem effect and hence inconsequential to the ballistic performance of the composite armor.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340211
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    Masthead (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994) 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340301
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    Analysis of a reactor with surface renewal for poly(ethylene terephthalate) synthesis (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 190-200 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A mathematical model of a polycondensation reactor that can be used in the final stage for poly(ethylene terephthalate) (PET) is established and compared with experimental data obtained from a laboratory scale reactor with film renewal. Detailed side reactions are considered along with the diffusional removal of the small molecules through thin film. Among several kinetic constants, the polycondensation reaction rate constant k1(= k8) and diester group degradation reaction rate constant k7 have an influence over the degree of polymerization. The values of k1(= k8) and k7 for 0.05 wt% Sb2O3 were obtained as curve-fit values: (1) k1(= k8) = 3.4 × 106 exp(- 18.500/RT′) (L/mol-min); (2) k7 = 1.3 × 1011 exp(- 37,800/RT′) (min-1). Effects of the film exposure time, reduced pressure of vacuum, temperature, the initial terephthalic acid (TPA)/ethylene glycol (EG) mole ratio, the initial degree of polymerization, and catalysts were well explained by the model.
    Additional Material: 12 Ill.
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    URL: http://dx.doi.org/10.1002/pen.760340304
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    Entrance effects for power-law fluid (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 209-212 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Entrance pressure losses for the creeping flow of a power-law fluid are calculated for an abrupt contraction of ratio 2, 4, 8 and ∞ for both the axisymmetric and planar cases using P2P1 and P+2P1 finite elements. Contrary to some earlier findings in the literature, the entrance pressure loss obtained by using the two different types of finite elements, both of which satisfy the Babus̆ka-Brezzi condition, are found to converge to the same results. The present results also confirm that the variational method of Duda and Vrentas gives excellent upper bounds for both the axisymmetric and planar cases with infinite contraction ratio.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340306
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    Semianalytical solution for epoxy-amine curing in the presence of nonisothermal effects (1994)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 405-413 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The curing of epoxy-amine polymer has been modeled by the reaction of functional groups, and the mole balance of these is governed by a set of six nonlinear differential equations. In this work, we have first developed a complete analytical solution for isothermal curing. For nonisothermal curing, we have divided the domain of hydroxyl group concentration β into small increments Δβ and adopted our analytical results for this domain. In addition, we solved the energy balance equation analytically and obtained the temperature rise for Δβ. We have compared our results with those obtained from the Runge Kutta numerical solutions. We have shown that our semianalytical technique is about a thousand times more efficient and faster.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760340505
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