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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 157 (1988), S. 177-187 
    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: Die Kinetik der alkalischen Hydrolyse von Glimmer-Acrylnitril-Pfropfcopolymeren wurde untersucht. Die Abhängigkeit des Verseifungsgrades von der Alkalikonzentration und der Hydrolysezeit wurde bestimmt. Chemische und spektroskopische Techniken wurden zur Bestimmung des Hydrolysemechanismus herangezogen.
    Notes: Kinetics of alkaline hydrolysis of mica-acrylonitrile graft copolymers was studied. The dependence of alkali concentration and the time of hydrolysis on the degree of saponification was determined. Chemical and spectroscopical techniques were used to determine the mechanism of hydrolysis.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 187 (1991), S. 1-10 
    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: Eine neue Klasse von Urethan-Acrylat-Monomeren wurde durch Umsetzung von Diisocyanaten wie Toluylendiisocyanat (TDI) und Hexamethylendiisocyanat (HMDI) mit Hydroxyethylmethacrylat oder Hydroxypropylmethacrylat und gesättigten Alkoholen wie Stearylalkohol oder Decanol hergestellt und durch IR- und NMR-Spektroskopie charakterisiert. Durch radikalische Polymerisation dieser Monomeren wurden Acrylatpolymere mit Urethanseitengruppen erhalten, die IR-spektroskopisch, viskosimetrisch und thermisch charakterisiert wurden.Die thermodynamischen Parameter des Polymerabbaus wurden berechnet; ein möglicher Abbaumechanismus wird vorgeschlagen.
    Notes: A new class of urethane-acrylic monomers was synthesized from diisocyanates such as toluylene diisocyanate (TDI) and hexamethylene diisocyanate (HMDI), unsaturated alcohols like hydroxyethyl methacrylate (HEMA), hydroxypropyl methacrylate (HPMA), and saturated alcohols such as stearly alcohol and decanol. The monomers were characterized by IR and NMR spectroscopy. Urethane pendent acrylic polymers, obtained by polymerizing these monomers, were characterized by IR, solubility viscosity, and thermal studies. The thermodynamic parameters for the degradation were calculated and a probable degradation mechanism is proposed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 1659-1667 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Casein-g-poly(vinyl acetate) was synthesized using potassium persulfate as initiator. Changes in monomer concentration, initiator concentration, backbone concentration, and temperature were effected. The rate of total conversion of monomer, the rate of homopolymerization and graft copolymerization, the grafting efficiency and the percentage of grafting were calculated. The grafting results were discussed in the light of grafting efficiency and percentage of grafting. They were found to be lower in the case of casein-g-poly(vinyl acetate) when compared to those of casein-g-poly(butyl acrylate).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 180 (1979), S. 2923-2928 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(acrylonitrile-co-methyl methacrylate) films were oxidized in an air oven and in an oxidation chamber at temperatures of 80 to 200°C. Differential thermal analysis of these oxidized films showed that the exothermic peaks increased with increasing oxidation temperature. The change of viscosity, the insolubility in dimethylformamide and IR analyses indicate both intramolecular and intermolecular reactions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1799-1806 
    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
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1313-1319 
    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: Kinetics of grafting of poly(butyl acrylate) onto gelatin was studied with H2O2 - ascorbic acid redox systm. Percent grafting, grafting efficiency, Rg, and Rh were determined as a function of time, temperature, initiator, monomer, and backbone concentration. It was found that Rg depends on first power of monomer concentration and 0.5 power to the initiator concentrations. A detailed kinetic scheme is proposed to explain these results.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 329-339 
    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: Poly(butyl acrylate) has been graft copolymerized onto casein using potassium peroxydisulfate-ascorbic acid as the initiating system. The proof of grafting has been obtained by ninhydrin test and IR studies. The effects of synthetic variables in the graft copolymerization have been discussed in the light of percent grafting, grafting efficiency, and the rates of polymerization.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 2123-2133 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyacrylamide has been grafted onto casein in phosphate buffer medium using potassium peroxodisulfate as initiator. The influence of synthetic variables on percent grafting, grafting efficiency, rates of conversion of monomer, and the rates of graft copolymerization have been discussed. A possible kinetic scheme based on experimental results has been derived.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1723-1731 
    ISSN: 0887-624X
    Keywords: “living” radical polymerization ; iniferter ; macroiniferter ; polyurethane ; 1,1,2,2-tetraphenylethane-1,2-diol ; acrylonitrile ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel polyurethane iniferter, synthesized from equal moles of toluene diisocyanate and 1,1,2,2-tetraphenyl-1,2-ethanediol, was used to polymerize acrylonitrile to assess whether it proceeded via a “living” radical polymerization mechanism. From the kinetic results, the rate of polymerization could be expressed as Rpα[BPT]0.96[AN]1.64. The increase of number-average molecular weight with increase of both conversion and polymerization time, the bimodal molecular weight distribution in gel permeation chromatography and the increase of molecular weight in the post-polymerization of polyacrylonitrile confirm that the present tetraphenylethane-based polyurethane iniferter follows a “living” radical polymerization mechanism. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 901-913 
    ISSN: 0887-624X
    Keywords: monotropism ; liquid crystalline polyurethanes ; differential scanning calorimetry ; cross-polarized optical microscopy ; X-ray diffraction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2′-Azobis-[2-cyano-(4-ethylphenol)] (ABCP) was prepared from parahydroxyacetophenone, using hydrazine sulfate and sodium cyanide. Biphenylol ester of ABCP, 2,2′-azobis-[2-p-biphenyloxy-(4-ethylphenol)] (BECP) was synthesized via the acid route. Combined liquid crystalline polyurethanes (CLCPUs) were synthesized from 1,6-diisocyanatohexane (HDI) and BECP in dimethylformamide (DMF) at 110°C under nitrogen atmosphere. The effect of partial replacement of BECP by 4,4′-dihydroxy biphenyl (DHBP) on liquid crystalline (LC) properties was studied. The polymers were characterized by proton and 13C NMR, FTIR, and UV spectroscopy. Elemental analysis were done for determining the percentage content of C, H, and N and the molecular weights of the polymers were determined by gel permeation chromatography (GPC). Thermogravimetric investigations (TGA) of the polyurethanes (PUs) were performed to study the decomposition. The LC nature of the PUs was confirmed by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Cross-polarized optical microscopy studies demonstrated the existence of two distinct crystalline morphologies, a spherulitic morphology with high mole ratio of DHBP and a thread-like crystalline morphology with that of BECP. All the PUs synthesized showed a LC nature with a wide temperature range. Partial replacement of BECP by DHBP changed the mesomorphic nature, transition temperature, and temperature range of the mesophase. © 1995 John Wiley & Sons, Inc.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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