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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 41-53 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of graft copolymer on the demixing of solutions of two immiscible homopolymers and critical conditions for emulsion formation were studied. The graft copolymer used in the present work consists of one backbone poly(vinyl acetate) (PVAc) and one branch polystyrene (PS). PVAc and PS of various degrees of polymerization were used as immiscible homopolymers. The common solvent was benzene. When the concentration of homopolymer blend was not sufficiently higher than the critical concentration for demixing of the blend solution, no stable emulsion was formed, even when a considerable amount of graft copolymer was present, and the added graft copolymer merely reduced the demixing rate. However, as the blend concentration was increased, a stable emulsion could readily be obtained by addition of rather small amounts of graft copolymer. The radius of emulsion droplets was inversely proportional to the weight ratio of the graft copolymer to the dispersed component polymer, in accordance with the theoretical prediction. It was concluded that the emulsions were stabilized against coagulation by graft copolymer molecules fixed strongly as a monolayer on the interface of the emulsion.
    Additional Material: 11 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2251-2261 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of poly(vinyl alcohol) (PVAL) with V(V), i.e., pentavalent vanadium ion, was studied in aqueous H2SO4 medium. The viscosity change of reaction mixture with time showed a peculiar feature owing to formation of labile complex between V(V) and PVAL and the subsequent decomposition of the complex. On the other hand, the change of viscosity disappeared when NaOH was added during the reaction to neutralize H2SO4 in the reaction mixture. Under a suitable condition, the reaction mixture set to a gel as a result of complex formation. It appeared that reactive sites in PVAL responsive to complexing with V(V) were 1,2-glycol unit and 1,2-ketoalcohol unit resulting from the oxidation of 1,2-glycol by V(V). The rate of oxidation was increased with increasing H2SO4 concentration. The main-chain scission of PVAL took place to an insignificant extent, unless the reaction condition was severe. Based on the results obtained a reaction mechanism has been proposed.
    Additional Material: 13 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 451-460 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(vinyl alcohol) (PVAI) was oxidized by ceric ion, Ce(IV), in aqueous HNO3 medium at different temperatures and found to be degraded as a result of selective cleavage of the 1,2-glycol unit existing in PVAl. The rate of oxidation increased with increasing temperature. The aldehyde groups formed at the ends of the degraded polymer upon oxidation were relatively stable at 0°C. With rise of temperature, the aldehyde groups reacted either with excess of Ce(IV) to carboxylic acids or with hydroxyl groups of PVAl molecules to give acetal linkage. When the acetalization predominated over the oxidation to carboxyl group, gelation of the reaction mixture was observed. Based on these results, a plausible mechanism of oxidation of PVAl with Ce(IV) and the subsequent reactions is discussed.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 27-40 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Precipitation of poly(methyl methacrylate) (PMMA) from dimethyl sulfoxide solution by addition of water as a precipitant was studied in the presence of a well-characterized graft copolymer of poly(vinyl alcohol) (PVA). The graft copolymer which had been prepared by a radiation method and freed from PMMA and PVA homopolymers had one PMMA branch whose length was nearly equal to that of the PVA backbone. Even when such an amount of water was added to PMMA solution as to cause all the PMMA to precipitate from the solution, the precipitation was prevented by the presence of relatively small amounts of the graft copolymer. With decreasing molecular weight of PMMA, the effect of protection became more pronounced. When the precipitation was prevented, the solution was transformed into a stable emulsion. The mechanism of protection against precipitation was discussed on the basis of the results obtained and electron microscopic photographs of the emulsion particles. It was concluded that the particles of the precipitated homopolymer were covered by a monolayer of the graft copolymer, resulting in prevention of coagulation.
    Additional Material: 11 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2397-2397 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1829-1839 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the oxidation of poly(vinyl alcohol) (PVAL) by potassium persulfate (KPS) in aqueous solutions showed that the decomposition of KPS was greatly enhanced by the presence of PVAL, its hydroxyl groups being oxidized to ketones in a yield of about one mole of ketone from one mole of KPS. The decomposition rate of KPS was found to be given by the equation, -d[S2O82-]/dt = k[S2O82-] [PVAL]1/2, which was essentially the same as in the oxidation of alcohols of low molecular weight by persulfate ion. The occurrence of gelation of PVAL solutions and graft copolymerization of methyl methacrylate (MMA) onto PVAL in the presence of KPS was evidence for PVAL radical as an intermediate species in the oxidation of PVAL. A characterization study was also carried out for the reaction products of the graft copolymerization of MMA onto PVAL with KPS in dimethyl sulfoxide solution.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 755-760 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 323-335 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Criteria for formation and flocculation of micelles from pure graft copolymers were investigated in single selective solvents by turbidimetry with the use of two series of graft copolymers from poly(vinyl acetate) (PVAC), i.e., PVAC-styrene graft copolymers with one branch and PVAC-methyl methacrylate graft copolymers with one and several branches. These graft copolymers could be completely coagulated through two processes in the selective solvents which had widely different ⊖ temperatures. The first process is the formation of micelles. One sequence, i.e., either backbone or branch of the graft copolymers, becomes desolvated under conditions similar to those for the corresponding homopolymer. This results in formation of the core of the micelle, the other soluble sequence extending from the surface of the core into the solvent phase. As the soluble chains cover the micelle core, no macroscopic phase separation occurs, but a stable dispersion is formed. The second process is that the micelle becomes too unstable to exist as dispersed when the solvency of the medium for the soluble sequence decreases to a certain degree. As a result, flocculation of the micelle finally takes place.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 715-725 
    ISSN: 0887-6266
    Keywords: polyethylene ; ion implantation ; surface structure ; wear ; hardness ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene (PE) film was implanted with 1000-keV Ar+ ions to a fluence of 5 × 1014 ions/cm2 under high vacuum conditions (2.5 × 10-6 torr) and the film surface was investigated by means of microhardness and microwear measurements, and FTIR/ATR, Raman, and XPS techniques. Ion implantation significantly increased the subsurface hardness and also significantly improved the microwear resistance of the polymer. The implanted surface region of the film was found to consist of two distinct layers. One was the outermost carbon layer with a thickness of the order of 10 nm. In this layer, ca. 75% of carbon atoms were combined by graphitic sp2 and diamond-like sp3 bonds, and the remaining 25% had chemical links with oxygen atoms. Spectroscopic data suggested that the sp2-bonded carbons segregated in graphite-like clusters containing imbedded oxygen atoms, interconnected by the sp3-bonded carbons. The other was the subsurface layer resulting from PE oxidation after ion-beam treatment. This layer was characterized by high contents of O—H and C=O groups as well as ester and double bonds. The chemical composition of the layer was uniform and did not vary over the layer thickness of about 1.4 μm. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 715-725, 1998
    Additional Material: 10 Ill.
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