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  • 1975-1979  (12)
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  • 1
    Publication Date: 1977-09-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    Publication Date: 1975-06-01
    Print ISSN: 0006-2960
    Electronic ISSN: 1520-4995
    Topics: Biology , Chemistry and Pharmacology
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 10 (1977), S. 1117-1124 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 14 (1975), S. 2542-2546 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 3151-3156 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two methods were investigated for the preparation of poly(dimethyl biphenylene) in a search for polymers combining good solubility with sufficiently high chain extension to produce a lyotropic nematic phase. The Ullmann reaction was used to condense 4,4′-diiodo-3,3′-dimethyl biphenyl and the corresponding 2,2′-dimethyl derivative with copper, and 4,4′-dibromo-2,2′-dimethyl biphenyl was polymerized using the coupling reagent, bis(1,5-cyclooctadiene)nickel(0), developed by Semmelhack. The Ullmann polymers were completely soluble in CHCl3 but only partially soluble in toluene, whereas earlier work had indicated similar polymers of higher molecular weight to be completely soluble in toluene. All the polymers produced were of low molecular weight and no evidence of the nematic phase was found by polarized light microscopy for CHCl3 solutions over the concentration range 6.8-25% by weight.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 17 (1979), S. 601-607 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 883-894 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In co[poly(ethylene terephthalate)-p-oxybenzoate] containing 30 mole % oxybenzoate units, the ethylene terephthate units crystallize. The copolymer melts in the temperature range 180-210°C to form a nematic phase which, at a higher temperature, transforms to an isotropic liquid. The latent heat of the first transition is 5 cal/g, and the thermodynamic melting temperature, 247°C, is essentially that expected for a random copolymer of this composition. The nematic → isotropic transition occurs at 244°C, with an enthalpy change of 3.2 cal/g (10% of the heat of fusion of poly(ethylene terephthalate)). We conclude that semiflexible polymers form a nematic phase which is rather highly disordered. The model of the nematic phase treated by Flory is modified to increase its entropy through incorporation of chain bends (which must be correlated in position and direction with those in neighboring molecules). This increases the chain extension, as measured by the fraction (1-f) of collinear chain bonds, required to form the nematic phase. For binary polymer-solvent systems, an appropriate scaling of f values leaves the phase diagram as predicted by Flory's treatment essentially unchanged.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 393-407 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation of statistical chain segments in the amorphous regions of a semicrystalline polymer can be characterized quantitatively by x-ray diffraction. A calculated background (which is orientation independent) must be subtracted, which requires that the intensity profile of the amorphous halo be measured on an absolute scale. Application is illustrated to samples of isotactic polystyrene which were isothermally crystallized at fixed elongation. These samples differ from those of the previous study due to the unintentional introduction of a small amount of crystallinity (0.25% to 1%) which serves as tie points in the drawing operation, giving a stronger amorphous orientation. Preferred orientation of the amorphous chain segments is rapidly depleted during the first few percent of crystallization. The crystallite orientation distribution is quite sharp, and broadens only slowly with crystallization. These results imply that, for the crystallization conditions employed, the crystallite orientation must be determined by nuclei which are formed at the earliest stages of the crystallization process.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 2091-2101 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The aromatic Polyamide-hydrazide, Monsanto X-500, has been studied by light scattering in dimethyl sulfoxide, a thermodynamically good solvent. The unperturbed dimensions, (〈r02〉av/M)1/2 = 1.93 × 10-8 at 25°C., indicate a rather highly extended chain. The persistence length falls in the range 35-63 Å, which corresponds to a length of between two and four formula units. This is considerably smaller than the values which have been reported for the aromatic polyamides, poly(p-benzamide) and poly(p-phenylene terephthalamide). X-500 appears to approximate coil-like behavior at a molecular weight of 45,000. Theoretical predictions, based upon the 〈r02〉av/bL ratio, are compared with the observation that no evidence for an anisotropic phase has been found in X-500 solutions in dimethyl sulfoxide at polymer volume ranging from 0.12 to 0.19 (depending upon the concentration of added LiCl).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1649-1659 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rheological and rheo-optical data are reported for the poly(terephthalamide of p-aminobenzhydrazide), X-500, in dimethyl sulfoxide solutions in the concentration range 0.2 to 6.0 g/100 ml. The objective of these measurements is to seek evidence of shear-induced isotropic → nematic phase transition. Three types of measurement, Couette, cone and plate, and capillary rheometer, all indicate that this system exhibits flow instabilities at high shear rates and concentrations. In this region both the viscosity and the primary normal stress difference decrease with time under shear. In the capillary rheometer the apparent viscosity is smaller for shorter capillaries and, for short capillaries, there is a range of shear rates in which plug flow and a coiled extrudate are observed. These instabilities may arise from the existence of a mixture of isotropic and nematic phases. At lower shear rates, where the flow behavior appears normal, the concentration dependence of the flow birefringence increases at a critical polymer concentration Cp* This value is in reasonable accord with the concentration corresponding to the change of slope of logη (measured at low shear rate) vs. logCp. Both the latter measurements appear to be sensitive to the onset of the phenomenon, which may be due to a shear-induced transition or the rheological effect of chain entanglements.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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