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  • Polymer and Materials Science  (273)
  • 1985-1989  (273)
  • 1960-1964
  • 1925-1929
  • 1985  (273)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 131 (1985), S. 145-155 
    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 application of electron irradiated polypropylene granulate as a nucleating agent in extrusion has recently been suggested. This article discusses the chemical characterisation of such an electron treated granulate. Since the irradiation is carried out under atmospheric conditions, the relationship between decomposition, crosslinking and oxidation products has been determined. Oxidation is confined principally to the outermost molecular layers and leads to the formation of carbonyl groups via peroxide intermediates. As well as specific group tests, ESCA has been used to measure the degree of oxidation and for indirect determination of vinyl groups after bromination.
    Notes: In jüngster Zeit wird der Einsatz von elektronen-bestrahltem Polypropylengranulat als Nukleierungsmittel bei der Extrusion vorgeschlagen. Die vorliegende Arbeit beschäftigt sich mit der chemischen Charakterisierung der elektronen-bestrahlten Granulate. Da die Bestrahlung unter atmosphärischen Bedingungen stattfindet, werden nicht nur der Zusammenhang von Abbau und Vernetzung, sondern auch Oxidationsprodukte bestimmt. Die oxidative Schädigung findet hauptsächlich in den oberen Moleküllagen statt und führt über peroxidische Zwischenprodukte zur Entstehung von Carbonylgruppen. Neben für funktionelle Gruppen spezifischen Nachweismethoden wird die oberflächen-spezifische ESCA-Methode zur Erfassung des Oxidationsgrades und zur indirekten Vinylgruppenbestimmung nach der Bromierung eingesetzt.
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  • 2
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Mittels der Feldgradienten-Impuls-NMR wurden die Selbstdiffusionskoeffizienten Ds der Makromolekiile in an Luft γ-hestrahlten Polyethylenproben in Abhangigkeit von Ds von der Schichttiefe gemessen. Auf Basis der chemischen Reaktionen der Radikale wird eine Gleichung abgeleitet, die die Abhangigkeit von 8,von der Schichttiefe in Gebieten mit kinetisch und diffusiv kontrollierter Oxidation beschreibt. Der Einflulß der Kristallinitat sowic der Intensitat und Temperatur der Bestrahlung auf die Dicke der oxidiertcn Schicht wird untcrsucht.
    Notes: Layer-by-layer study of commercial polyethylene samples, γ-irradiated in air, was carried out by measuring the selfdiffusion coefficient Ds of macromolecules by means of pulsed field gradient NMR. On the basis of chemical reactions of the radicals an equation is obtained, describing the dependence of Ds on the layer depth in the kinetic and diffusive oxidation regions. The effect of crystallinity, radiation intensity and temperature on the thickness of the oxidized layer is examined.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mechanical creep and creep recovery in small shearing deformations have been studied in unligated clots formed with both thrombin and ancrod. In thrombin clots, both A binding sites (which interact with “a” sites to link monomer units within a protofibril) and B sites (which interact with “b” sites to form links between protofibrils) are exposed to enable formation of linkages; in ancrod clots, only the A sites are exposed. Fine clots (with minimal lateral aggregation of protofibrils), coarse clots (with substantial aggregation of fibril bundles), and clots of intermediate coarseness were compared. Fine thrombin clots showed less creep at short times but more creep at long times than coarse or intermediate clots and had more irrecoverable deformation relative to the initial elastic deformation. Ancrod clots had greater irrecoverable deformation than the corresponding thrombin clots, both fine and coarse. The permanent deformation in fine ancrod clots was enormous, corresponding almost to fluid character; the rate of permanent deformation was larger than that in fine thrombin clots by more than two orders of magnitude. For all types of clots, differential measurements of compliance (or its reciprocal, elastic modulus), as well as the applicability of the Boltzmann superposition principle to calculation of creep recovery, showed that the overall density of structure remained constant throughout the mechanical history; i.e., if structural elements were breaking, they were reforming at the same rate in different configurations. The possibility that the weakness of ancrod clots is attributable to partial degradation of α-chains rather than absence of Bb linkages was eliminated by comparisons of clots made with thrombin, ancrod, and ancrod plus thrombin; the last two showed identical partial degradation of α-chains (by gel electrophoresis), but the first and third had essentially identical initial elastic moduli and creep behavior. Two alternative mechanisms for irrecoverable deformation in fine clots are discussed, involving rupture of protofibrils and slippage of twisted segments, respectively.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 24 (1985), S. 1549-1572 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The binding of the antitumor agent CC-1065 to a variety of poly- and oligonucleotides was studied by electronic absorption, CD, and resistance to removal by Sephadex column chromatography. Competitive binding experiments between CC-1065 and netropsin were carried out with calf-thymus DNA, poly(dI-dC) · poly(dI-dC), poly(dI) · poly(dC), poly(rA) · poly(dT), poly(dA- dC) · poly(dG-dT), and poly(dA) · 2poly(dT). CC-1065 binds to polynucleotides by three mechanisms. In the first, CC-1065 binds only weakly, as judged by the induction of zero or very weak CD spectra and low resistance to extraction of drug from the polynucleotide by Sephadex chromatography. In the second and third mechanisms, CC-1065 binds strongly, as judged by the induction of two distinct, intense CD spectra and high resistance to extraction of drug from the polynucleotide, by Sephadex chromatography in both cases. The species bound by the second mechanism converts to that bound by the third mechanism with varying kinetics, which depend both on the base-pair sequence and composition of the polynucleotide. Competitive binding experiments with netropsin show that CC-1065 binds strongly in the minor groove of DNA by the second and third mechanisms of binding. Netropsin can displace CC-1065 that is bound by the second mechanism but not that bound by the third mechanism. CC-1065 binds preferentially to B-form duplex DNA and weakly (by the first binding mechanism) or not at all to RNA, DNA, and RNA-DNA polynucleotides which adopt the A-form conformation or to single-strand DNA. This correlation of strong binding of CC-1065 to B-form duplex DNA is consistent with x-ray data, which suggest an anomalous structure for poly(dI) · poly(rC), as compared with poly(rI) · poly(dC) (A-form) and poly(dI) · poly(dC) (B-form). The binding data indicate that poly(rA) · poly(dU) takes the B-form secondary structure like poly(rA) · poly(dT). Triple-stranded poly(dA) · 2poly(dT) and poly(dA) · 2poly(dU), which are considered to adopt the A-form conformation, bind CC-1065 strongly. Netropsin, which also shows a binding preference for B-form polynucleotides, also binds to poly(dA) · 2poly(dT) and occupies the same binding site as CC-1065. These binding studies are consistent with results of x-ray studies, which suggest that A-form triplex DNA retains some structural features of B-form DNA that are not present in A-form duplex DNA; i.e., the axial rise per nucleotide and the base tilt. Triple-stranded poly(dA) · 2poly(rU) does not bind CC-1065 strongly but has nearly the same conformation as poly(dA) · 2poly(dT) based on x-ray analysis. This suggests that the 2′-OH group of the poly(rU) strands interferes with CC-1065 binding to this polynucleotide. The same type of interference may occur for other RNA and DNA-RNA polynucleotides that bind CC-1065 weakly.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 24 (1985), S. 2301-2332 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Physical studies and conformational analysis of human glycophorin A suggest a revised model for its molecular organization, self-association, and interactions with the erythrocyte membrane. Intrinsic viscosity has been used to study, under more physiological conditions, the monomer-dimer equilibrium demonstrated previously by polyacrylamide-SDS gel electrophoresis. The results show that the equilibrium persists in the absence of detergent and support earlier indications that the dimer is probably the physiologically relevant form and that it is promoted by salt, inhibited by conventional denaturants, and abolished by carboxymethylation.Combined application of CD, fitted to the poly-(L-lysine) model spectra of Greenfield and Fasman, and conformational prediction, by the statistical method of Chou and Fasman and the stereochemical approach of Lim, suggests five helical sequences in glycophorin A: Arg-39 to Tyr-52 (A); Gln-63 to Glu-70 (B); Glu-72 to Leu-89 (C); Ile-95 to Lys-101 (D); and Leu-118 to Asn-125 (E). Sequence A occurs only at low pH and may be stabilized by favorable noncovalent interactions of O-linked tetrasaccharide side chains. The other four helices all occur in the dimeric form of glycophorin A at physiological pH and ionic strength. Sequence D is destroyed by trypsin, and is also lost on conversion to the monomeric form of the glycoprotein at low ionic strength. Sequence E is denatured by 6M guanidine hydrochloride/4M urea. Sequences B and C, which are separated by a single proline residue, are stable under all these conditions.Dimerization of the major, hydrophobic helical sequence, (C) may be promoted and directed by an adjacent short sequence of intermolecular parallel β-sheet (Leu-90 to Tyr-93). It is proposed that these two structures span the lipid bilayer in vivo, and that helices B and D lie, respectively, along the outer and inner surfaces of the membrane. Molecular organization in the N- and C-terminal regions of the molecule is discussed in terms of evidence from the present work and from other recent investigations.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 36 (1985), S. 203-215 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Stress corrosion cracking of unalloyed steels in liquid ammoniaIn this work is reported on investigations about stress corrosion cracking of steels in liquid ammonia aimed at ascertaining the parameters and the ranges within which they are effective, finding the mechanism responsible for the damage of spherical pressure vessels and developing protective measures. The investigations are based partly on corrosion tests in which welded Jones samples of various unalloyed and low alloyed steels in different states of heat treatment were immersed in ammonia for long periods in a spherical ammonia storage vessel.For laboratory tests we used an apparatus specially developed to enable round tensile test bars to be tested in liquid ammonia under CERT conditions at the open circuit potential and under electrochemical control. In these tests selectively added impurities were determined quantitatively by gas chromatography.The results of the investigations show that the oxygen content of the ammonia has a decisive influence on the initiation of stress corrosion cracking in unalloyed steels. Even low O2 concentrations (ßß2 ppm) lead to a risk of stress corrosion cracking. Addition of water in sufficient quantity inhibits the stress corrosion cracking.The water concentration needed to inhibit corrosion differs according to the material concerned (StE 355: 〉 500 ppm; H I: 〉 650 ppm; StE 460: 〉 1000 ppm H2O). The different stress corrosion behaviour of the investigated steels under residual and operating stresses shows their different sensitivity. So in absence of stress relieve heat treatment only Jones samples of StE 355 remained crack-free.Investigations into the influence of potential on crack formation showed that the damage follows an anodic crack formation mechanism, since it is capable of being reinforced anodically and inhibited cathodically. Similarly the inhibitive effect of water is reduced by anodic polarization. But stress corrosion cracking cannot be induced by anodic polarization alone, i.e. in the absence of O2.As a practical conclusion it may be said that the presence of oxygen - even in traces - must be avoided.Addition of water inhibits stress corrosion cracking; these additions are therefore recommended wherever they are possible.Containers should be made of StE 355 and they should be stress relieve annealed.Cathodic protection is considered appropriate, but the practicability under operating conditions has to be still investigated.
    Notes: In dieser Arbeit wird über Untersuchungen zur SpRK von Stählen in flüssigem Ammoniak berichtet, deren Ziel es war, Einflußgrößen und ihre Wirkgrenzen zu bestimmen, Aufschluß über den Mechanismus der an Kugeldruckbehältern aufgetretenen Schäden zu erlangen und Schutzmaßnahmen zu ermitteln. Zu diesem Zweck wurden langzeitige Auslagerungsversuche mit geschweißten Jones-Proben aus verschiedenen unlegierten und niedriglegierten Stählen unterschiedlicher Wärmebehandlungszustände in einer Ammoniakkugel durchgeführt.Für Laborversuche wurde eigens eine Apparatur entwickelt, mit der Untersuchungen in flüssigem Ammoniak an Rundzugstäben unter CERTConstant Extension Rate Test-Bedingungen beim Freien Korrosionspotential und unter elektrochemischer Kontrolle durchgeführt werden konnten. Gezielt zugesetzte Verunreinigungen wurden hierbei mittels eines Gaschromatographen quantitativ bestimmt.Aus den Untersuchungen geht der entscheidende Einfluß des Sauerstoffgehalts im Ammoniak auf die Entstehung von Spannungsrißkorrosion an unlegierten Stählen hervor. Bereits geringe O2-Mengen (ßß 2 ppm) bewirken eine Spannungsrißkorrosionsgefahr. Wassergehalte können die Spannungsrißkorrosion inhibieren. Hierbei werden bezüglich der erforderlichen Menge Unterschiede zwischen den einzelnen Werkstoffen sichtbar (StE 355: 〉 500 ppm, H I: 〉 650 ppm, StE 460: 〉 1000 ppm H2O). Eine werkstoffseitige Differenzierung wird auch in bezug auf den Einfluß von Eigen- und Betriebsspannungen deutlich. Lediglich Jones-Proben aus StE 355 blieben ohne Spannungsarmglühung rißfrei.Versuche zur Potentialabhängigkeit der Rißbildung weisen aus, daß die Schädigung einem anodischen Rißbildungsmechanismus folgt, da sie anodisch verstärkt und kathodisch verhindert werden kann. Ebenso wird die inhibitive Wirkung des Wassers durch eine anodische Polarisation eingeschränkt. Jedoch ist durch anodische Polarisation allein, d.h. ohne Gegenwart von O2, Spannungsrißkorrosion nicht zu erzielen.Für die Praxis kann zusammengefaßt werden: Sauerstoffgehalte - auch in Spuren - sind zu vermeiden.Wasserzusatz inhibiert die Spannungsrißkorrosion; Zusätze von Wasser sind daher - soweit möglich - zu empfehlen.Behälter sollen aus StE 355 gebaut und spannungsarm geglüht werden.Kathodischer Schutz ist denkbar, sofern es gelingt, diesen in der Praxis zu verwirklichen.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1573-1578 
    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: Crosslinked epoxy resins, tetraglycidyl 4,4′-diamino diphenyl methane cured with 4,4′-diamino diphenyl sulfone, were soaked in water at either 25°C or 70°C for varying lengths of time. The infrared spectra and DSC thermograms were obtained for samples that were soaked, or soaked and dried. There was a monotonic decrease in exothermic reaction energy with water content. The glass transition was also lowered, although samples soaked at 70°C showed a leveling in the Tg around 115°C. When the soaked samples were dried, the exothermic reaction energy showed near reversibility for samples soaked at 25°C while the 70°C samples were highly irreversible. IR of the latter samples showed that the 70°C water soaking resulted in reaction of some of the unreacted epoxide groups that remained after the initial cure.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 2869-2882 
    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: Dielectric loss measurements at four temperatures and as a function of frequency are presented for the poly(vinyl acetate) (PVAc) systems containing small concentrations of cholesterol, cholesteryl acetate, cholesteryl oleate, cholesteryl nonanoate, cholesteryl benzoate, cholesteryl oleyl carbonate, p-methoxy benzilidine-p-n-butyl aniline, diphenyl ether, and cetyl acetate. For the first five systems, the α-relaxation temperature for sure PVAc was found to be increased in the presence of the said additives. The results of the dielectric depolarization spectroscopy at 1 kHz and the dynamic mechanical analysis also conform with these observations. It is inferred that the segmental motion in PVAc is hindered by these first five additive molecules through a specific dipolar interaction. These additives are therefore described as antiplasticizers to PVAc as they extend the glassy region over a wider temperature interval. The analysis of the dielectric data to give the dielectric decay function and the β parameter reveals that the two types of the additives, viz., plasticizers and antiplasticizers, can be distinguished by the opposite signs obtained for the ratio Δβ/ΔC, where C is the concentration. The analysis based on the WLF theory shows that the WLF reference temperature T0 is higher than that for pure polymer if the additive is an antiplasticizer while the same is lower for the plasticizing additives. The apparent enthalpy of activation for the dielectric relaxation process is found to be higher in the case of additives which show antiplasticization of PVAc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 4417-4429 
    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 behavior of nylon-6 tire cords at elevated temperature has been evaluated. The heat treatment of cords at 200°C for 16 h was found to reduce their tensile properties considerably. This has been attributed to the decrease in average molecular weight and change in molecular weight distribution as ascertained by fractionation studies. Heat setting of cords in the temperature range of 180-210°C without any applied tension showed some decrease in tensile properties. This has been ascribed to the higher degree of shrinkage of the cords and hence increased chain folding in the molecular structure. However, irrespective of time and temperature of heat treatment, shrinkage was reduced with increasing tension on the cord. Effect of heat setting on density and crystallinity was also evaluated.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 875-885 
    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: Copolymers of sodium acrylate and N-methyl-, N-isopropyl-, N-n-butyl-, and N-t-butylacrylamide were prepared. The viscosities of these copolymers in 0.01% and 2.00% NaCl and their resistances to shear were compared with those of several partially hydrolyzed polyacrylamides. The poly(N-alkylacrylamide-co-sodium acrylate demonstrated somewhat better retention of viscosity in brine than did analagous partially hydrolyzed polyacrylamides. N-alkyl substitution increased sensitivity to shear in low salt solutions.
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