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  • Polymer and Materials Science  (39)
  • COMMUNICATIONS AND RADAR  (2)
  • 1990-1994  (28)
  • 1970-1974  (13)
  • 1950-1954
  • 1920-1924
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 129-137 
    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.
    Additional Material: 4 Tab.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Neurotoxic peptides from venoms of scorpions and honey bees exhibit a consensus pattern in the two disulfide bridgings related to the sequence portions Cys-X-Cys and Cys-X-X-X-Cys. A revised three-dimensional structure of charybdotoxin, as determined by two-dimensional nmr spectroscopy, confirms that the consensus cystine dislocation generates in all these toxins a common structural element, i.e., the cystine-stabilized α-helical (CSH) motif, which may be correlated with their common ion channel blocking activity.
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Um den Mechanismus der Katalyse der Polyvinylamin-Kupfer(II)-Chelate bei der Auslösung der Vinylpolymerisation zu klären, wurden die Stabilitätskonstanten dieser Chelate durch Anwendung einer modifizierten BJERRUMschen Methode gemessen, und die Konzentration der chemischen Spezies wurde auf Grund der Chelattheorie abgeschätzt. Anhand dieser Ergebnisse wurde die Aktivität der Polyvinylamin-Kupfer(II)-Chelate bei der Polymerisation von Acrylnitril und von Methylmethacrylat bei verschiedenen pH-Werten diskutiert.
    Notes: In order to clarify the mechanism of catalysis of polyvinylamine-copper(II) chelates on the initiation of vinyl polymerizations, stability constants of these chelates were measured by applying a modification of BJERRUM'S method, and each concentration of the chemical species was estimated on the basis of the chelate theory. From these results, the activity of the polyvinylamine-copper(II) chelates for the polymerization of acrylonitrile and methyl methacrylate at different pH values was discussed.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 175 (1974), S. 1001-1005 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 295-303 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By treating a blue-colored solution of poly(vinyl alcohol) (PVA), iodine and boric acid with an anion exchange resin, a solution consisting only of the polyiodide ion bound to the PVA matrix was obtained. In order to re-establish the equilibrium between polyidodide, I2 and I-, the bound polyiodide ions decomposed to I- and I2. When this happend at temperatures below 10°C, only I- was released from the PVA matrix with I2 remaining in it, and a new equilibrium state was reestablished. However, above 20°C all polyiodide ions were decomposed without recovering the equilibrium of the reaction. In this case both I2 and I- were released from the PVA matrix. Based on these findings a new mechanism for the formation and decomposition of polyiodide ions was deduced. From the initial and equilibrium concentrations of the polyiodide ions at 5 and 10°C, approximate dissociation constants to I- (free) and I2 (bound) were estimated.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die durch Kupfer(II)-Chelate initiierten Polymerisationen von Acrylnitril, Methylmethacrylat sowie von Styrol wurden in Gegenwart von Tetrachlorkohlenstoff untersucht. Als Liganden wurden polymerer und dimerer Vinylalkohol, d. h. Polyvinylalkohol und 1,3-Propandiol, gewählt. Es ergab sich, daß diese Initiatorsysteme die Polymerisation von Methylmethacrylat und Styrol wirkungsvoll auslösen konnten. Die Aktivität des polymeren Chelats wurde in Abhängigkeit von verschiedenen Metall/Ligand-Molverhältnissen des Initiatorsystems, den pH-Werten und der Temperatur untersucht. Auf Grund der Ergebnisse wurde der Mechanismus für die Radikalerzeugung diskutiert.
    Notes: The polymerizations of acrylonitrile, methyl methacrylate and styrene initiated by copper(II) chelates were studied in the presence of carbon tetrachloride. Polymeric and dimeric compounds of vinyl alcohol, that is poly(vinyl alcohol) and 1,3-propanediol were chosen as ligands. It was found that these systems could initiate the polymerization of methyl methacrylate and styrene effectively. The activity of the polymer chelate was estimated by varying the metal/ligand mole ratio of the initiator system, the pH values and the polymerization temperature. From the results, the mechanism of the free-radical formation was discussed.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3069-3076 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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 recrystallization of amorphous cellulose at various relative humidities was studied to clarify the relation between the amount of adsorbed water in cellulose and the molecular motion by the DSC method. The initial recrystallization kinetics of amorphous cellulose at various relative humidities were observed on the basis of the exothermic peak between 380° and 470°K in a DSC curve. The recrystallization occurred easily by conditioning at higher than 80% R.H., but hardly by conditioning at lower than 65% R.H. These facts suggest that the conformation of cellulose seems to be easily changeable if cellulose has a moisture regain which is approximately comparable to capillary water. When the Avrami equation was applied to the slope of calorific value versus conditioning time at higher than 80% R. H., it also appeared that the mode of recrystallization growth of amorphous cellulose exposed to water vapor is one-dimensional.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2809-2813 
    ISSN: 0887-624X
    Keywords: Malachite Green vinyl polymer ; ionic conductivity ; photoinduced switching ; single-ionic ; carrier generation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of bis[4-(N,N-dimethylamino)phenyl]-4-vinylphenylmethanenitrile (vinyl Malachite Green leuconitrile) with methyl methacrylate or ω-methoxyoligo(oxyethylene) methacrylate have been synthesized, aiming at designing one-component-type organic polymers for photoswitchable ion-conducting films. The triphenylmethanenitrile copolymers with ω-methoxyoligo(oxyethylene) methacrylate were found to undergo ionic-conductivity switching by turning on and off UV light at ambient temperature, owing to their low glass transition temperature. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 181-185 
    ISSN: 0887-624X
    Keywords: poly(bisthiazole-imide) ; heterocyclic polyimide ; solubility ; high-temperature polymers ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1243-1254 
    ISSN: 0887-624X
    Keywords: tetraphenylporphyrin-containing polymer ; homopolymer ; water-soluble polymer ; radical polymerization ; manganese(III) complex ; ligand substitution reaction ; anionic ligand ; thiocyanate ; electrostatic effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A vinyl monomer containing the pendant tetraphenylporphyrin (TPP) group, 4-vinyltetraphenylporphyrin (VTPP), was synthesized. A homopolymer (PVTPP) which is insoluble in water, and three water-soluble polymers were obtained by radical polymerization. The water-soluble polymers are two anionic polymers (PVPTSPP and PVTPP-StSO3) and a cationic polymer (PVTPP-VPyM). PVPTSPP has sulfonic acid groups in a TPP group and very high charge density. PVTPP-StSO3 was obtained by copolymerization of VTPP and sodium 4-styrenesulfonate. PVTPP-VPyM was obtained by quarternarization of a copolymer of VTPP and 4-vinylpyridine. Polymeric manganese(III) complexes (PMn-VTPP, PMnVPTSPP, PMnVTPP-StSO3, and PMnVTPP-VPyM) were prepared from the polymers and manganese acetate. The acetate ligand in PMnVTPP can be easily substituted by another ligand such as Cl-, AcO-, OH-, and SCN-. The substitution reaction occurs in the interface between water and chloroform. The sulfonated homopolymer, PMnVPTSPP, cannot incorporate with anionic ligands because of the strong electrostatic repulsion. In the anionic copolymer, PMnVTPP-StSO3, the ligand substitution reaction with SCN ligand needs activation energy of 53 kJ/mol. In the cationic polymer complex, PMnVTPP-VPyM, the OH ligand can be easily substituted with the SCN ligand and the equilibrium constant of the reaction was estimated at 1.38 × 10-3. © 1994 John Wiley & Sons, Inc.
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