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  • Polymer and Materials Science  (4,900)
  • 2015-2019
  • 1995-1999  (4,900)
  • 1975-1979
  • 1996  (4,900)
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  • 2015-2019
  • 1995-1999  (4,900)
  • 1975-1979
Year
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 333-339 
    ISSN: 0887-624X
    Keywords: reactivity ratios ; microstructure ; 13C-NMR spectroscopy ; (vinyl acetate)/(glycidyl methacrylate) copolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Vinyl acetate)/(glycidyl methacrylate) (V/G) copolymers were prepared by free radical solution polymerization in benzene. Copolymer composition was determined by 1H-NMR spectroscopy. Comonomer reactivity ratios were calculated by Kelen-Tüdos (KT) and error-in-variables (EVM) methods. The values reactivity ratios calculated by these methods are rV = 0.03 ± 0.01; rG = 38.9 ± 6.20 (KT) and rV = 0.03 ± 0.002; rG = 39.5 ± 1.97 (EVM). The microstructure of V/G copolymers in terms of the distribution of V and G centered was obtained from 13C{1H}-NMR spectra using the carbonyl carbon resonance signals of V as well as G units. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 117-124 
    ISSN: 0887-624X
    Keywords: polyimide ; polyamide ; adamantane ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,3-Diaminoadamantane (I) was used as a monomer with various aromatic dicarboxylic acyl chlorides and dianhydrides to synthesize polyamides and polyimides, respectively. Polyamides having inherent viscosities of 0.10-0.27 dL/g were prepared by low-temperature solution polycondensation. The polyamides were soluble in a variety of solvents such as N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAc), N-methyl-2-pyrrolidone (NMP), pyridine, dioxane, and nitrobenzene. These polyamides had glass transition temperatures in the 179-187°C range and 5% weight loss temperatures occurred at up to 354°C. Polyimides based on diamine I and various aromatic dianhydrides were synthesized by the two-stage procedure that included ring-opening to form polyamic acids, followed by thermal conversion to polyimides. The polyamic acids had inherent viscosities of 0.14-0.38 dL/g. The glass transition temperature of these polyimides were in the 245-303°C range and showed almost no weight loss up to 350°C under air and nitrogen atmosphere. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 141-148 
    ISSN: 0887-624X
    Keywords: polyacrylic acid ; silicone rubber membrane ; plasma-induced graft polymerization ; homobifunctional membrane ; 1,1-diphenyl-2-picryhydrazyl ; surface modification ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyacrylic acid (PAA) was grafted onto the surface of silicone rubber membrane (SR) by plasma-induced graft copolymerization (PIP). Ar-plasma was used to activate the surface of SR. Also, a determination was made of the influences of plasma treatment power, pressure, time, grafted copolymerization reaction time, and monomer concentration on polymerization yield. The surface properties of SR were measured by ATR-FTIR, ESCA, and SIMS. In those analyses, the elemental composition and different carbon bindings on the surface of SR were examined by ESCA with the amount of O1s/C1s being approximately 0.7 at 60 s by Ar-plasma treatment (60 W, 200 mtorr). The peroxide group introduced on SR was measured via 1,1-diphenyl-2-picryhydrazyl (DPPH). The optimum amount of peroxide groups was 6.85 × 10-8 mol/cm2 at 60 s of Ar-plasma treatment. The peroxide group (33D peak) was introduced onto the surface of SR by negative spectra of SIMS analysis after SR treatment by Ar-plasma. An increase was obtained in grafted polymerization yield with a region of 5 to 50% (v/v) of acrylic acid aqueous solution. Both sites of polyacrylic acid were detected after staining by toluidine blue O. That is, a homobifunctional membrane was developed via this surface modification method. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
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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. 261-270 
    ISSN: 0887-624X
    Keywords: chemically modified polymers ; addition reactions ; carboxybetaines ; reaction mechanisms and kinetics ; pyridines ; imidazoles ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed study of the synthesis of betaine products that result from addition reactions of poly (4-vinylpyridine) and poly (N-vinylimidazole) as well as of their model compounds, with α,β-unsaturated monocarboxylic acids is presented. A reaction mechanism based on experimental observations and proved by kinetic analysis is proposed. It consists of two reactions: the addition, which involves two molecules of acid and leads to X+B--like structures, where the cation X+ results from the addition of the amino nitrogen to the double bond of acid and B- is the carboxyl anion, and an equilibrium reaction between X+B- and the betaine structure X±. The latter occurs only in protic solvents and is coupled with the addition reaction. The process was especially investigated in methanol, because this solvent allows determination of the kinetic parameters. Some values of the addition rate constants are given. The study is based on 1H-NMR measurements and observations. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 301-303 
    ISSN: 0887-624X
    Keywords: thermosensitive polymer ; water soluble polymer ; polymer modification reaction ; poly(vinylamine) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
    Additional Material: 1 Ill.
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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. 157-163 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From data in the literature on relative rates of copolymerization it has been possible to evaluate two constants, Q and e, characteristic of an individual monomer, which appear to account satisfactorily for its behavior in copolymerization. The constant Q describes the “general monomer reactivity” and is apparently related to possibilities for stabilization in a radical adduct. The constant e takes account of polar factors influencing copolymerization.
    Additional Material: 5 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 357-365 
    ISSN: 0887-624X
    Keywords: processable polyimides ; poly(pyromellitimide)s ; rigid-rod polyimides ; polyimides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From imidazole-blocked 2,5-bis[(n-alkyloxy)methyl]-1,4-benzene diisocyanates and pyromellitic dianhydride a series of new rigid-rod polyimides (Cn-PY-PI; n = 4, 6, 8) having linear and flexible (alkyloxy)methyl ((SINGLE BOND)CH2OCnH2n + 1; n = 4, 6, 8) side chains were prepared and characterized and their properties were measured and discussed with regard to effects of side chains. Incorporation of the side chains onto the rigid main chain greatly enhanced the solubility and fusibility of the polymers, and melting point of C8-PY-PI was determined to be 277°C. The UV-VIS absorption behavior was independent of side-chain length. TGA thermograms revealed a two-step pyrolysis behavior, in which the side chains split off separately at lower temperatures. X-ray diffractograms showed that all the polyimides are crystalline at room temperature. Sharp reflections in small-angle region obviously indicated the presence of a layered crystal structure. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 481-492 
    ISSN: 0887-624X
    Keywords: poly(benzobisthiazoles) ; sulfonated poly(benzobisthiazoles) ; rigid rod polymers ; polyelectrolytes ; thermally stable polymers ; conducting polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic polyelectrolytes based on sulfonated poly(benzobisthiazoles) (PBTs) have been synthesized by a polycondensation reaction of sulfo-containing aromatic dicarboxylic acids with 2,5-diamino-1,4-benzenedithiol dihydrochloride (DABDT) in freshly prepared polyphosphoric acid (PPA). Several sulfonated PBTs, poly[(benzo[1,2-d:4,5-d′]bisthiazole-2,6-diyl)-2-sulfo-1,4-phenylene] sodium salt (p-sulfo PBT), poly[(benzo[1,2-d:4,5-d′]bisthiazole-2,6-diyl)-5-sulfo-1,3-phenylene] sodium salt (m-sulfo PBT), their copolymers, and poly[(benzo[1,2-d:4,5-d′]bisthiazole-2,6-diyl)-4,6-disulfo-1,3-phenylene] potassium salt (m-disulfo PBT), have been targeted and the polymers obtained characterized by 13C-NMR, FT-IR, elemental analysis, thermal analysis, and solution viscosity measurements. Structural analyses confirm the structures of p-sulfo PBT and m-disulfo PBT, but suggest that the sulfonate is cleaved from the chain during synthesis of m-sulfo PBT. m-Disulfo PBT dissolves in water as well as strong acids, while p-sulfo PBT dissolves well in strong acids, certain solvent mixtures containing strong acids, and hot DMSO. TGA indicates that these sulfonated PBTs are thermally stable to over 500°C. Free-standing films of p-sulfo PBT, cast from dilute neutral DMSO solutions, are transparent, tough, and orange in color. Films cast from basic DMSO are also free standing, while being opaque and yellow-green. p-Sulfo PBT was incorporated as the dopant ion in polypyrrole, producing conductive films with conductivities as high as 3 S/cm and electrical anisotropies as high as 10. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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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. 517-518 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 721-728 
    ISSN: 0887-624X
    Keywords: polyurethane ; metal ions ; synthesis ; coordination ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyurethane organometallic complexes based on novel diols, bis[N-[[2-hydroxyphenyl]methylene]hydroxylethyleneamino]-copper(II) (DBSICu), were synthesized successfully. The products are elastomeric glassy materials or powders. Similar to other polyurethane elastomers, these coordination block copolymers exhibit 2-phase microstructure and thermoplastic properties. It is interesting to note that some of these polyurethanes show a Schlieren pattern under the polarizing optical microscope. The liquid crystalline properties of DBSICu and the coordination polymers are studied in detail in this study. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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