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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 5 (1967), S. 1077-1081 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2603-2612 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Graft copolymerization of maleimide onto polyethylene and ethyl cellulose films by using its sublimation vapor was carried out under ultraviolet irradiation in the presence or absence of air; the effect of air or additives on the grafting reaction and on the nature of the grafted films was investigated. The extent of grafting gradually approached a fixed value, in spite of the continuous ultraviolet irradiation. Air retarded the grafting reaction but did not suppress the reaction nor alter the final extent of grafting. Benzoquinone showed no inhibiting effect on the grafting. The grafted polymaleimide was found to be amorphous, even though ultraviolet irradiation produces a highly crystalline homopolymer in the solid phase as well as in the liquid phase. The results were discussed in comparison with those of the vapor-phase grafting under γ-ray irradiation; the reaction is attributed to the vapor-crystal equilibrium of monomer and to the formation of short-chain crosslinks.
    Additional Material: 9 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1175-1182 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced copolymer grafting of acenaphthylene and maleic anhydride onto polyethylene or EVA film in the vapor phase was carried out and the effect of comonomer sorption on the grafting was studied. When polyethylene film was used as a backbone polymer, the sorption of the binary monomers during the grafting increased linearly as the grafting reaction proceeded. The marked increase was probably caused by the formation of a grafted layer. Particularly, the sorption of maleic anhydride was brought about by the existence of a grafted layer. In grafting onto EVA film, the content of maleic anhddride in the grafted copolymer increased with the increasing content of vinyl acetate in EVA. Continuous measurements of sorption of the comonomers onto EVA and grafted EVA films were carried out by use of an electrobalance. The distinctive feature of the sorption was that the equilibrium sorption of acenaphthylene or maleic anhydride onto the grafted EVA film increased and the diffusion constants for both comonomers decreased markedly with increasing percentage of graft. The copolymer grafting was explained from these results by assuming that the monomer molecules are supplied to the propagating chain ends mostly through a sorbed state on the polymer film.
    Additional Material: 9 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3145-3153 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical structure of polymers produced by the γ irradiation of monovinylsilanes was studied. γ-ray addition polymerization of monovinylsilanes such as trialkylvinylsilane was very slow, and only the liquid oligomers were formed from them by large radiation dose. The presence of silethylene or silmethylene linkage was ascertained in these polymers by infrared absorption spectroscopy and 1H-NMR measurement, even when no Si—H bond existed in the monomers. The polymers were supposed to be produced by addition polymerization with intervening silalkylene linkage.
    Additional Material: 4 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 33-37 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 823-828 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1363-1375 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solid-state polymerization of maleimide by γ- and ultraviolet irradiation was carried out in binary systems with succinimide, maleic anhydride, and acenaphthylene. Polymaleimide obtained from the solid-state polymerization of maleimide by γ-rays was amorphous, while that obtained from the solid-state polymerization by ultraviolet rays was highly crystalline. In the maleimide-succinimide system the rate of polymerization reached a maximum nearly at the eutectic composition when the polymerization was carried out by γ-irradiation. With ultraviolet irradiation the rate of polymerization became higher with increasing content of succinimide in the feed. In the maleimide-maleic anhydride system a copolymer of both constituents was formed by γ-irradiation, but almost no homopolymer was produced. On the other hand, two kinds of polymers, a crystalline copolymer and an amorphous one, were produced by ultraviolet irradiation. The results were compared with those obtained from the copolymerization in solution. In the maleimide-acenaphthylene system the main products with ultraviolet irradiation was the dimer of acenaphthylene.
    Additional Material: 11 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2223-2235 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Charge-transfer complexes in solutions of ethylmaleimide and stilbenes have been characterized by spectroscopy. The stoichiometric compositions of these complexes have been shown by Job's method to be 1:1 molar complexes. The value of the equilibrium constant K for complex formation of ethylmaleimide with stilbene derivative increases in the following probable order: ethylmaleimide-stilbene ≪ ethylmaleimide-dimethylaminostilbene (DMAS) 〈 ethylmaleimide-aminodimethylaminostilbene (ADMAS). From the calculations of the electron density of the highest occupied level for the stilbenes, the charge transfer in ethylmaleimide-DMAS and ethylmaleimide-ADMAS is attributed to n → π transition, while the charge transfer in ethylmaleimide-stilbene is attributed to n → π transition. Copolymerization was carried out by γ-irradiation in benzene or THF solutions of the comonomer pairs. The alternating tendency of copolymerization was larger in the ethylmaleimide-DMAS system than in the ethylmaleimide-stilbene system. This can be explained by assuming resonance structures in the transition state of addition reaction of DMAS to the propagating ethylmaleimide unit. In the copolymerization of ethylmaleimide with ADMAS, the effect of the penultimate unit was more important than in that with DMAS.
    Additional Material: 13 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2463-2467 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 439-454 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The graft copolymerizations onto the preirradiated polypropylene fibers of gaseous vinyl chloride and also of gaseous vinylidene chloride were carried out. The fibers were preirradiated with γ-rays from a 60Co source at -78°C. in air to a total dose of 8 X 105 rad, and were thus presumed to contain peroxide radicals which were active in grafting at ordinary temperature. The volume decrease of monomers at constant pressures due to the sorption and the grafting reaction was followed automatically at temperatures ranging from -10 to 80°C. The net monomer consumption through the grafting process was estimated by subtracting the volume change due to the sorption from the total volume change of monomers. In general, the extent of grafting was lower at the higher grafting temperature and the decrease of the grafting activity of fibers was also accelerated. The grafting was found to increase almost linearly with the logarithm of the reaction time and the logarithm of the radiation of the radiation dose to the fibers. The extent of grafting was also proportional to the vapor pressure of monomer at a given reaction temperature and was supposed to be controlled by the amount of the monomer adsorbed. Raising the irradiation temperature higher than 0°C. brought about a marked decrease in the activity of preirradiated polypropylene. The grafting activity was successfully retained by the polymer for at least a fortnight at -78°C.
    Additional Material: 11 Ill.
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