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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1375-1383 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Changes in properties of linear aromatic heterocyclic polymers of the polyimide class after introduction of ester linkages into their dianhydride component and of the oxygen and sulfur atoms into their diamine component have been studied. Thermomechanical, dilatometric, thermographic characteristics and x-ray diffraction patterns of poly(ester amic acids) and polyester-imides have been investigated. On heating, poly(ester amic acids) and amorphous polyesterimides exhibited a peculiar effect of self-orientation of macromolecules. The x-ray diffraction patterns of unoriented films indicate that they exhibit axial-planar texture with the c axis of macromolecules in the film plane. The formation of the texture is preceded by mutual arrangement of macromolecules, i.e., by a precrystallization process beginning in the amorphous state. Because of this, on heating at temperatures ranging from 200 to 380°C, polyester-imides yield highly crystalline products. Crystallographic parameters of the polymer lattices on x-ray diffraction patterns and dichroism of absorption bands in polarized infrared spectra, the most probable conformations of macromolecules of some polyesterimides are proposed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2651-2657 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Styrene-butadiene rubber (SBR) charged with 50 phr of HAF carbon black has been found to show a positive temperature coefficient of resistivity close to 0.07/°C at 27°C. Beyond a point (75°C) of minimum conductivity, however, it behaves as a normal noncrystalline semiconductor with a resistivity which decreases with rise of temperature with an activation energy of 0.56 eV. Blending the composition with poly(vinyl chloride) (PVC) shifts the minimum towards lower temperatures. The descending branch of the conductivity versus reciprocal absolute temperature characteristic is probably associated with thermal expansion of tunnelling paths separating the conducting carbon particles.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 3115-3124 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of methyl methacrylate (MMA) initiated by tri-n-butylborane (TBB) was studied in the presence of various organic halides (R′X). It was found that R′X accelerated the polymerization of MMA. Aliphatic halides were more effective than aromatic halides. Cocatalytic effects of butyl halides decreased in the order: n-BuI 〉 n-BuBr 〉 n-BuCl; n-BuBr ⋍ sec-BuBr 〉 i-BuBr 〉 tert-BuBr. In the polymerization of MMA by TBB-n-BuI, the initial rate of polymerization was found to be proportional to the concentration of MMA and to the square root of the concentration of TBB-n-BuI. The apparent activation energy was 5.3 kcal/mole. From this and other results, it was assumed that the polymerization of MMA by this initiator system proceeds by a radical mechanism via a weak complex between TBB and R′X; alkyl radicals are formed by the interaction of R′X with TBB. The TBB-R′X system can initiate the polymerization of MMA and AN, but is ineffective in the polymerization of styrene.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1049-1063 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular core binding energies have been measured by ESCA for a series of copolymers of tetrafluoroethylene and ethylene. Detailed analysis of the results demonstrates the utility of ESCA for determination of copolymer compositions and for providing information on important structural features for these copolymers.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2073-2081 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eleven samples of carboxylic polysaccharides were studied. The activity coefficients γ have been measured for monovalent (Na+) and divalent (Ca2+) counterions. There is no specific influence of the structure of the chain on γ values. Agreement with theoretical values confirms the rigidity of the chain; for low charge density, the theoretical treatment seems to be incorrect. Selectivity is discussed in term of selectivity coefficient KNaCa and free energy of exchange ΔGNaCa; ΔGNaCa is linearly related to the charge density but KNaCa which characterizes the competition of the two counterions is sensitive to the nature of the chain. The carboxymethylamyloses present a larger selectivity whose origin is not discussed here. The last point treated is the intrinsic constant of dissociation of polyacids. The pK0 values are practically independent of the nature of the polyelectrolyte and of the charge density; the values are close to the pK0 of monomeric unit and are not affected by the position of —COOH in the anhydroglucose ring.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 587-610 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymer containing 2-vinylpyridine-trimethylsilyl methacrylate, styrene-2-vinylpyridine, and styrene-trimethylsilyl methacrylate blocks as well as terpolymers containing the styrene2-vinylpyridine-trimethylsilyl methacrylate blocks were synthesized by initiation of the appropriate monomers sequentially both with butyllithium and sodium. These polymers were subjected to hydrolysis by which the acrylate ester segment is converted to the free acid and to the reaction with methyl iodide, which quaternizes the pyridine segment; finally the hydrolyzed and quaternized polymers were subjected to dehydrohalogenation with external base. The properties of these block polymers and blends of the styrene-containing block copolymers were examined, especially in regard to their suitability as reverse osmosis desalination membranes.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2265-2274 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several new types of polybenzimidazoquinazolines with a different recurring unit have been prepared by solution polycondensation in polyphosphoric acid followed by heating at elevated temperature under reduced pressure. The polymers thus obtained were light yellow to brown powdery materials hardly soluble in common organic solvents and soluble in concentrated sulfuric acid. The inherent viscosity of the polymers ranged from 0.1 to 0.58 and showed good thermal stability.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 3503-3510 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of isomerization of butenes by boron trifluoride with acetic acid or methanol as cocatalysts have been re-examined. The results, over a wide concentration range, and at temperatures from -20 to +20°C, are consistent with previous data, but it is shown that the previously suggested mechanism cannot apply. By using deuterated acetic acid as cocatalyst it has been found that isomerization exactly parallels protonation, which is consistent with a mechanism involving a classical carbonium ion.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1375-1386 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrolytic polymerization of acrylates and methacrylates in methanol solution containing lithium acetate as electrolyte was investigated under currents ranging from 10 to 100 mA. Polymer yield increases up to a limiting current value, beyond which it decreases. This abnormal behavior is discussed. A free-radical mechanism is suggested.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 3161-3168 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemical and thermal geometrical isomerizations of monoazo compounds have been studied in polystyrene-n-butylbenzene compositions. Cis-trans isomer ratios established by light absorption were found to depend on matrix viscosity. Where the compositions were above their respective glass temperatures, all thermal isomerizations conformed to first-order kinetics. Where compositions were below their respective glass temperatures, the initial isomerization rates were abnormally fast, decaying to normal first-order processes after substantial amounts of reaction had taken place. These effects have been interpreted in terms of the vitreous properties of polystyrene.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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