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  • Polymer and Materials Science  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 1947-1953 
    ISSN: 0021-8995
    Keywords: 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: During the past few years it has been reported that a number of metal-organic compounds show outstanding effectiveness as stabilizers against the oxidative deterioration of polyolefins and other polymers. This may seem surprising in view of the well known catalytic effect of such compounds on the oxidation of organic materials. Indeed, it has been observed that a given metal compound can act as a stabilizer in one system and as an antistabilizer in another. Even in a single system the compound may simultaneously retard one mode of oxidation and accelerate another. For example, the copper chelate of α,α-(ethylenedinitrilo)-di-o-cresol retarded the formation of carbonyl groups and accelerated scission during the photoöxidation of polyethylene. It is the purpose of this paper to consider a number of examples of this sort drawn from the field of metal-organic stabilizers.1 Any comprehensive theory of oxidation and antioxidation should be able to encompass such curious anomalies.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0021-8995
    Keywords: 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: Many derivatives of phenyl salicylate turn yellow when they are exposed, in solution, to ultraviolet light. This limits their usefulness as ultraviolet stabilizers for plastics. Evidence is presented to support the postulation that the yellowing is due to the formation, by a photochemical ortho rearrangement, of a derivative of 2,2′-dihydroxybenzo-phenone. Aromatic salicylates, such as 2,6-dialkylphenyl salicylate, in which the ortho rearrangement is blocked, are found to be nonyellowing stabilizers, although less effective than the better yellowing varieties, such as p-octylphenyl salicylate. Loss of stabilizer by volatilization, either in compounding or during subsequent exposure, is shown to be an important factor in limiting the effective performance of the stabilizer.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 2251-2260 
    ISSN: 0021-8995
    Keywords: 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: The ordinary methods for obtaining a rapid estimate of the useful life of a plastic, extrapolations from tests conducted at higher temperatures or at lower stabilizer concentrations than those of actual use, lead to serious errors in estimating the useful life of some stabilized polypropylene compositions. Two methods for obtaining more reliable rapid estimates of useful life have been explored and are reported here: (1) measurement of physical and chemical changes, such as weight loss, stabilizer loss, density increase, dyeability increase, and formation of carbonyl or hydroperoxide groups, which occur during the prefailure stages of oxidative deterioration at the temperature of interest (of these, measurements of stabilizer loss appear the most promising); (2) thermal development of the prefailure oxidative damage initiated at the temperature of interest. This method needs further exploration.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 2453-2465 
    ISSN: 0021-8995
    Keywords: 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: Cellulose esters which have a high degree of esterification are readily crystallizable by simple heat treatments. Such esters include cellulose triacetate, cellulose tripropionate, and mixed cellulose triesters. X-ray diffraction analysis shows distinct crystal patterns for these crystalline cellulose esters, and differential thermal analysis shows strong melting peaks. X-ray diffraction analysis of secondary cellulose esters, that is, esters having a substantially lower degree of esterification, shows very diffuse patterns which are only slightly indicative of crystalline structure. Differential thermal analysis, on the other hand, shows strong endothermic peaks which appear to indicate melting of crystalline material. Once melted, secondary cellulose esters cannot be recrystallized easily by simple heat treatments, but it has been found that treatment with certain solvents will induce crystallization. For instance, precipitation of secondary cellulose acetate from acetic acid gave a material which showed two melting peaks by differential thermal analysis, and precipitation from acetone gave a material which showed a single melting peak. A secondary mixed ester, cellulose acetate butyrate, precipitated from acetone had three melting peaks. The coincidence of two of the peak temperatures of this ester with those of the separate triesters of acetic and butyric acids indicated a block rather than a random substitution into the cellulose chain.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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