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  • Polymer and Materials Science  (14,995)
  • Organic Chemistry  (2,690)
  • Inorganic Chemistry  (1,777)
  • 1995-1999  (19,462)
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Year
  • 11
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1581-1587 
    ISSN: 0887-624X
    Keywords: matrix polymerization ; polypyrrole ; chemical synthesis ; interpolymer complex ; water soluble polypyrrole ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidative matrix polymerization of pyrrole (Py) by Ce(IV) in the presence of Polyacrylic acid (PAA) has been studied to obtain water-soluble and insoluble products. The role of the PAA, Pyrrole, and Ce(IV) concentration, order of component addition, the structure of polymer matrix (PAA, Hydroxy Ethyl Cellulose (HES), Poly-N-vinylpyrrolidone (PVP)], and model unit of PAA (propionic acid), on the polymerization system were investigated.Interaction of PAA with insoluble polypyrrole (PPy) and the interpolymer complex formation were investigated along with the aggregation of PPy onto the matrix polymer followed by spectral shifts. FTIR results of insoluble products obtained from the PAA-Py-Ce(IV) system and solubility of the system is explained in light of the mechanism of the polymerization of pyrrole on the polymer matrix. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 415-426 
    ISSN: 0887-624X
    Keywords: thermotropic ; liquid crystalline polymer ; nematic ; synthesis ; characterization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of fully aromatic, thermotropic polyesters, derived from 3-phenyl-4,4′-biphenol (MPBP), nonlinear 4,4′-benzophenone dicarboxylic acid (4,4′-BDA), and various other comonomers was prepared by the melt polycondensation method and characterized for their thermotropic liquid crystalline behavior by a variety of experimental techniques. The homopolymer of MPBP with 4,4′-BDA had a fusion temperature (Tf) at 240°C, exhibited a nematic liquid crystalline phase, and had a narrow liquid crystalline range of 60°C. All of the copolyesters of MPBP with 4,4′-BDA and either 30 mol % 4-hydroxybenzoic acid (HBA), 6-hydroxy-2-naphthoic acid (HNA) or 50 mol % terephthalic acid (TA), 2,6-naphthale-nedicarboxylic acid (2,6-NDA) and low Tf values in the range of 210-230°C, exhibited a nematic phase, and had accessible isotropization transitions (Ti) in the range of 320-420°C, respectively. As expected, each of them had a broader range of liquid crystalline phase than the homopolymer. They had a “frozen” nematic, glassy order as determined with the wide-angle X-ray diffraction (WAXD) studies. The morphology of each of the “as-made” polyesters had a fibrous structure as determined with the scanning electron microscopy (SEM), which arises because of the liquid crystalline domains. Moreover, they had higher glass transition temperatures (Tg) in the range of 167-190°C than those of other liquid crystalline polyesters, and excellent thermal stabilities (Td) in the range of 500-533°C, respectively. © 1995 John Wiley & Sons, Inc.
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  • 13
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1727-1733 
    ISSN: 0887-624X
    Keywords: polymerizing detergents ; monomer micelles ; radical polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photo- and thermoinitiated radical polymerization of surface-active monomers with various structures was investigated in solution and in micelles in water. The relationship between kinetics and the structure of monomer associates was represented in the form of a universal curve. A model and kinetic description of polymerization in spherical micelles of monomer was proposed. The problem of micelle fixation by polymerization was solved. © 1995 John Wiley & Sons, Inc.
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  • 14
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1745-1749 
    ISSN: 0887-624X
    Keywords: viologen polymer ; lyotropic ; critical concentration ; synthesis ; characterization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [no Abstrat]
    Additional Material: 3 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1759-1765 
    ISSN: 0887-624X
    Keywords: compartmentalized ; seed ; emulsion ; oil-soluble initiators ; average radical number ; radical polymerization ; Kummer functions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Expressions for calculating the stationary state distribution of radicals in compartmentalized systems with a constant number of reaction loci containing an oil-soluble initiator are given. Besides pairwise formation of radicals in the particles, desorption and reabsorption, water phase termination, solubility of the initiator in the aqueous phase, and the possibility of formation of a single radical species are taken into consideration. The calculation is based on a probabilistic analysis leading to a third-order recurrence relation solved using confluent, hypergeometric Kummer functions. Some calculated curves illustrating the de-pendence of the average number of radicals per particle on various relevant parameters are included. © 1995 John Wiley & Sons, Inc.
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  • 16
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1807-1816 
    ISSN: 0887-624X
    Keywords: Oxetane ; oxirane ; photoinitiated cationic polymerization ; semiempirical molecular orbital calculation ; real-time FT-IR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinitiated cationic polymerization of oxetane, oxirane (epoxide), and a formulation of both was carried out and their reactivity compared. To investigate a formulated system of oxetane and oxirane in photoinitiated cationic polymerization, computational and experimental methods were used. In the computational study, we employed a semiempirical molecular orbital method (AM1). On the other hand, the reactivities of each system were evaluated and compared experimentally by a real-time FT-IR method. The computational study reveals that oxetane seems to polymerize in SN2 mechanism, but two possibilities, of SN1 mechanism through the α-cleavage and of SN2 mechanism through β-cleavage, are implied for oxirane. Using the real-time FT-IR method, the formulation of oxetane and oxirane was proved to possess rather high reactivities of oxetane toward photoinitiated cationic polymerization. The formulated system exhibited slightly lower number-average molecular weight than oxetane but higher than oxirane. These experimental observations are well explained in terms of the calculated reaction paths. © 1995 John Wiley & Sons, Inc.
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  • 17
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1849-1857 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; acrylic polymers ; core shell ; supermicron ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsion polymerization of large MMA/BA copolymer particles with narrow particle size distributions and core-shell structure is described. A series of sequential seeded growth emulsion polymerizations were used to obtain monodisperse particles with diameters of at least 3 μm, at 30% solids contents. Because the core and shell polymers used here were chemically similar, core-shell structures could not be verified by differential staining tech-niques. Core-shell structure was demonstrated by minimum film-forming temperature studies and by scanning electron microscopy in conjunction with energy dispersive x-ray analysis, using chlorine-labeled core polymers. © 1995 John Wiley & Sons, Inc.
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  • 18
    ISSN: 0887-624X
    Keywords: 2,4-ionene ; poly(quaternary ammonium)salt ; cobalt(II) phthalocyaninetetra-carboxylic acid ; cobalt(II) phthalocyanineoctacarboxylic acid ; mercaptoethanol ; autoxi-dation ; catalysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The promoting effects of 2,4-ionene on the cobalt(II) phthalocyaninetetracarboxylic acid-[CoPc(COOH)4] and cobalt(II) phthalocyanineoctacarboxylic acid-[CoPc(COOH)8] cata-lyzed autoxidation of 2-mercaptoethanol were studied. Dimerization of the CoPc(COOH)4 catalyst, combined with the disappearance of the catalytically inactive μ-peroxo complex and the appearance of substrate enrichment in the presence of 2,4-ionene, results in a 40-fold enhancement of the oxidation rate as compared with the polymer-free system. UV-VIS spectroscopy indicates that CoPc(COOH)8 is incapable of forming μ-peroxo complexes or 2,4-ionene-induced dimeric catalyst species under normal reaction conditions. Thus, it was possible to study exclusively the ionene-induced effect of substrate enrichment. Addition of 2,4-ionene to an aqueous CoPc(COOH)8 solution results in an activity enhancement by a factor of 2-3, which can be ascribed to substrate enrichment. Additionally, using mono-disperse ionene oligomers showed a molecular weight dependence of 2,4-ionene on the catalytic activity of CoPc(COOH)8, as was observed for the conventional 2,4-ionene/cobalt phthalocyaninetetrasodiumsulfonate system. The optimal polycation/catalyst ratios of both systems decrease with increasing chain length of 2,4-ionene, until a constant value is reached. This leads to the conclusion that the optimal polymer/catalyst ratios are predominantly determined by substrate enrichment. © 1995 John Wiley & Sons, Inc.
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  • 19
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1873-1879 
    ISSN: 0887-624X
    Keywords: combined catalyst system ; polymerization ; polyphenylacetylene film ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The simultaneous polymerization and formation of polyphenylacetylene film by Nd(P204)3-Fe(AA)3-Al(i-Bu)3 catalyst system have been investigated. The combined catalytic effects between rare earth phosphonates with MT(naph)x or Fe(AA)3 systems are first proposed and compared. The polymerization features and kinetic behaviors with Nd(P204)3-Fe(AA)3-Al(i-Bu)3 system are described and discussed. The combined catalytic effects have the following order, respectively: Fe ≫ Co 〉 Cr 〉 Mn-Ni, Nd(P204)3-Nd(P507)3 〉 Nd(P350)3 and Tb 〉 Sm 〉 Yb 〉 Ho 〉 Lu 〉 Dy 〉 Nd-Er-Pr 〉 Y-Tm 〉 Ce 〉 Gd 〉 La. The overall polymerization activation energy was found to be 20.8 kJ/mol showing coordination-anionic polymerization characteristic. PPA films so obtained are very similar to the rare earth ones. © 1995 John Wiley & Sons, Inc.
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  • 20
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1907-1912 
    ISSN: 0887-624X
    Keywords: substituted polyacetylene ; fluorine-containing polymer ; transition-metal catalyst ; gas permeability ; pervaporation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, properties, and membrane-separation functions of a novel fluorine-containing poly(phenylacetylene) were examined. The monomer used was [o-n-(perfluorohexyl)phe-nyl]acetylene, which has a rigid rod-like ortho-substituent. Polymers, whose intrinsic vis-cosities ([η]) were ca. 0.4-2.2 dL/g, were obtained in high yields with various W and Mo catalysts. The MoCl5-Ph3Sb catalyst achieved the highest [η] of 2.25 dL/g corresponding to an Mw over one million. The polymer was a brown solid soluble only in F -containing solvents such as m-(CF3)2C6H4. The oxygen permeability coefficient of the polymer mem-brane was 90 barrers, which is the second highest among those of ortho-substituted poly(phenylacetylenes). In the pervaporation of an ethanol-water mixture, the poly-mer membrane showed ethanol permselectivity [α(EtOH/H2O) = 1.7]. © 1995 John Wiley & Sons, Inc.
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