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  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Polyurethane-polymethacrylic acid multi-block copolymers were synthesized from tetraphenylethane based polyurethane iniferter. Number of polymethacrylic acid blocks and molecular weight of block copolymers increased with increasing polymerization time which proves that the formation of block copolymers is through a “living” radical mechanism. The multi-block copolymers obtained were converted into their sodium anionomers. The multi-block copolymers and their anionomers have been characterized by FTIR, FTNMR and DSC analysis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 37 (1996), S. 737-742 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Telechelic polyurethane cationomers containing end functional 4-vinylpyridinium moieties have been synthesized by the reaction of 4-vinylpyridine on 2-bromoethanol terminated polyurethane. The polyurethanes were characterized by FTIR, FTNMR and DSC studies. The introduction of ionic groups into the polyurethane shifts the Tg to lower temperatures, the shift in Tg further increases with increase in ionic groups.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Semi-Interpenetrating polymer networks (IPNs) of polyurethane anionomers (IPU) with Polyvinylchloride (PVC) were synthesized and characterized by Fourier-transform infrared spectrophotometer (FT-IR), thremogravimetric analysis (TGA) and mechanical studies. The synthesized semi-IPNs were found to be compatible. The hydrogen bonding interactions and the thermal stabilities are discussed based on FT-IR analysis and thermogravimetric analysis (TGA). Tensile strength and hardness increase with increasing NCO/OH ratio and ionic content of the polyurethanes.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1713-1721 
    ISSN: 0887-624X
    Keywords: polyurethane anionomers ; ionic diols ; methylene spacers ; TGA ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionic diols with varying methylene spacers were prepared from maleic anhydride and linear diols. Reaction across the unsaturated site by aqueous sodium bisulphite was used to prepare the ionic diols. Chain extended polyurethane ionomers were prepared by the reaction of prepolymer based on different polyols and diisocyanates with the ionic diols. The polyurethane anionomers were characterized by FT-IR and FT-NMR spectroscopy. The differential scanning calorimetric results show that Tg of the anionomers shifted towards low values as the ionic content in the polyurethane increases and as the length of the ionic diol increases. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 1237-1244 
    ISSN: 0887-624X
    Keywords: polyurethane ionomers ; iniferters ; “living” radical polymerization ; tetraphenylethane derivatives ; vinylbenzyl chloride ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyurethane iniferter prepared from isocyanate end capped prepolymer and 1,1,2,2-tetraphenyl-1,2-ethanediol, has been used to polymerize vinylbenzyl chloride to obtain polyurethane-polyvinylbenzyl chloride multiblock copolymers. Formation of the block copolymers proceeds with increase in both molecular weight and conversion with increasing polymerization time showing that the polymerization proceeds via a “living” radical mechanism. The block copolymers so obtained were converted into their cationomers by the treatment of triethylamine. The block copolymers and their cationomers have been characterized by FTIR, FTNMR, TGA, and DSC studies. The effect of thermal energy on the molecular weight of the macroiniferter in the absence of monomer has been studied in order to understand the mechanism of formation of the block copolymers. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1237-1244, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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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  • 7
    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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  • 8
    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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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 28 (1990), S. 307-314 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of 2-hydroxyethylmethacrylate (HEMA) and glycidylmethacrylate (GMA) are useful for contact lenses. Copolymerization of HEMA and GMA was carried out in dimethylformamide medium using benzoylperoxide as initiator at 60°C. The composition of HEMA and GMA in copolymers was estimated using 13C-NMR. The reactivity ratio of HEMA and GMA was found to be r = 0.73 and r2 = 0.98 by Finemann-Ross method and r1 = 0.74 and r2= 1.00 by Kelen-Tudos methods. The experimental values are in close agreement with theoretical value determined from Q-e scheme.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 33 (1994), S. 329-333 
    ISSN: 0959-8103
    Keywords: Leather shavings ; reinforcement ; nitrile rubber ; vulcanization ; mechanical properties ; swelling ; 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: Leather shavings have been used as filler in short fibre form for nitrile rubber reinforcement. Shavings neutralized with sodium bicarbonate and ammonia showed improved vulcanization characteristics and mechanical properties, whereas sodium hydroxide neutralized shavings exhibited poor properties. Swelling of the vulcanizates in water and 1% NaOH was found to increase with leather loading, whereas in MEK a reversed trend was observed. Thermogravimetric analysis indicates that the thermal stabilities of the vulcanizates fall between those of pure leather and gum nitrile rubber vulcanizate.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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