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  • Chemistry  (8)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 36 (1959), S. 305-312 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study was made of the polymerization of vinyl chloride using radioactive NaHS35O3 and KCl36O3 in a redox catalyst system. The object was to determine the fate of the catalysts as an aid to understanding part of the process of radical production and of the initiation of the polymerization. With the catalyst concentration usually used to conduct polymerizations, 0.3 atom of catalyst sulfur and about 0.08 atom of catalyst chlorine are chemically bound per PVC molecule. Increasing the catalyst concentration causes an increase in both the catalyst sulfur and catalyst chlorine incorporated into the PVC. The incorporation of the catalyst sulfur into the PVC, and the role of the sulfite in initiating the polymerization, can be explained by the free radical mechanism postulated for the addition of bisulfite to olefinic bonds. Only one-tenth of the catalyst chlorine bound to the PVC comes from the hypochlorite intermediate formed during the reaction. This suggests that the reactions of the sulfite with the chlorate, and with the chlorite formed during the reaction, produce most of the chain-initiating radicals.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 501-506 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers of vinyl chloride and vinyl acetate were prepared by tributylboroncatalyzed polymerizations at -15 and -40°C. The Alfrey-Price equations were used to calculate the monomer reactivity ratios to be expected in a free-radical propagation at -40°C. The experimentally determined monomer reactivity ratios were in good agreement with the theoretical values and support the concept of free-radical initiation by the tributylboron catalyst. Vinyl acetate interrupts the regular polymer sequences in polyvinyl chloride and interferes with the crystallizability of the polymer. The infrared D635/D692 absorbance ratio of the copolymers decreased approximately linearly with vinyl acetate content. The activation energy difference between syndio- and isotactic placements was calculated to be about 0.3 kcal./mole.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. S160 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The discovery has been made that when vinyl chloride is polymerized in certain aldehydes, a highly crystalline polyvinyl chloride is obtained. In butyraldehyde, low yields of a range of low molecular weight polymers are produced. Elemental analyses showed that they may be characterized by the formula: where n = 6-26. Support for this structure and molecular weight range was obtained from infrared and x-ray examinations of the polymers. The polymers are highly crystalline, as demonstrated by the x-ray and infrared results, and appear to have a syndiotactic structure. Variation of the polymerization temperature produced no measurable effect on the polymer stereoregularity. The ability of substituted aliphatic aldehydes to produce stereoregular PVC has shown a dependence on the electronegativity of the substituent in the aldehyde. Aliphatic aldehydes with an electron-releasing α-methyl group appear to give a more highly crystalline PVC. Aliphatic aldehydes with electron-withdrawing chlorine and oxygen atoms gives less crystalline PVC than do the corresponding α-methyl aldehydes. The dependence of the results upon polar effects suggests that the stereoregulating mechanism of the aldehydes involves association between the aldehyde, as a donor molecule, and the free propagating species, as the acceptor radical.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chloral was polymerized by means of cationic and anionic initiators and the products compared. Anionic catalysts readily produce high molecular weight polymer (DP ∼ 300-600), but a DP of only 200 could be produced with cationic catalysts. The anionic system apparently initiates and propagates polymerization much more readily than the cationic system. This effect is attributed to the inductive effects of the chlorine atoms on the chloral. Little difference was found when products of similar DP were compared as to x-ray diffraction pattern, infrared spectrum and tractability. This is believed due to the single type of structure which is sterically favored. Various cyclic compounds of chloral could not be made to undergo polymerization under cationic initiation. The conditions required to effect ring opening were too rigorous to enable polymerization to take place.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3741-3751 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Although dichloroacetaldehyde has only one chlorine less than chloral, the polymerization and polymer characteristics are quite different. Dichloroacetaldehyde is readily polymerized by Lewis acid catalysts to polymer with terminal hydroxyl groups. The catalyst BF3·Et2O, at 0°C., produces very high molecular weight polymer, in bulk polymerization. A DPn of about 400 is readily attainable. The characteristics of the polymerization indicate a cationic type, with greater dependence of DP upon chain termination rather than chain transfer. The polymer is readily end-capped by acetic anhydride, with a pyridine catalyst, to increase its thermal stability. Melting point, infrared spectra, and x-ray diffraction measurements confirm that the polymer produced under these conditions is amorphous. Cast films of the polymer could be only partially oriented The polymer is soluble in many common organic solvents.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 951-964 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study was made of the effect of polymerization temperature on the syndiotacticity of polyvinyl formate. Vinyl formate was polymerized with ultraviolet light initiation in the temperature range from -20 to +30°C. The value of (Ep  -  Et)/2 obtained, 4.5 kcal./mole, is characteristic of those values obtained by other workers for the free radical-initiated polymerization of vinyl acetate. A linear relationship was found to exist between the viscosities of the polyvinyl formates and those of the derived polyvinyl alcohols. The degree of polymerization of polyvinyl formate may be calculated from the equation: [η] = 4.42 × 10-3 DP0.63. The low temperature polymerization of vinyl for- mate results in more syndiotactic polymer, as shown by x-ray diffraction. Polyvinyl for-mate obtained at more elevated polymerization temperatures did not demonstrate the same degree of order. No difference was found between the infrared spectra of the polyvinyl formates. The polyvinyl alcohol derived from polyvinyl formate polymerized at low temperatures (0 to -35°C.) exhibits water resistance and forms a colored iodine complex similar to that obtained with the syndioactic polyvinyl alcohol derived from polyvinyl trifluoroacetate. Conventional polyvinyl alcohol and that derived from polyvinyl acetate polymerized at -30°C. do not exhibit the same properties. Minor differences in the 1,2-glycol content in the various polyvinyl alcohols do not account for the differences in the observations. The amount of head-to-head addition in various vinyl aliphatic esters seems to be related to the inductive strength of the acid portion of the ester. No difference was found between the crystallinities of the various polyvinyl alcohols, as measured by film density. Heat treatment increases the crystallinities about the same amount, but the water resistance of the stereoregular materials remains higher. From the good correlation between the observations made on polyvinyl formate and the derived polyvinyl alcohol, it is concluded that syndiotactic polyvinyl formate, and hence syndiotactic polyvinyl alcohol, is obtained by the low temperature free radical-initiated polymerization of vinyl formate. Increased syndiotacticity is more readily obtained in polyvinyl formate than in polyvinyl acetate, indicating the greater influence of inductive effect compared with the steric effect in controlling stereoregularity during free-radical propagation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polychloral diol, unlike polyoxymethylene diol, is not readily capped in the presence of alkali catalysts. Polychloral is capped under acid conditions by acid anhydrides and chlorides and does not appear to undergo degradation during the process. Evidence for end-capping is provided by infrared analysis in the case of the low DP polychloral, metachloral. End-capped polychlorals possess good stability towards hot dimethylformamide and good stability at elevated temperatures (255°C.). From the melting points of copolymers, polychloral itself is estimated to have a melting point of about 460°C. The high melting point is consistent with the rigidity of the polymer chain. A means of estimating the DP of the polymer is proposed, based on a form of endgroup analysis. By this technique, metachloral is estimated to have a DP of about 50.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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