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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 855-873 
    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 thermal decomposition of Thioped, a liquid polysulfide polymer based on dichloroethyl formal, was studied using pyrolysis-GC-MS. The nature and composition of the products of pyrolysis at 358 and 485°C are given. A striking feature of the product analysis is the presence of several disulfide compounds only at the higher decomposition temperature. The pyrolysis-GC of other liquid polysulfide polymers (LP-2, LP-32, LP-3, and LP-33) showed that molecular weight had only marginal effect on the product composition. Ionic and radical mechanisms were considered to account for the product formation. Isothermal and dynamic thermogravimetric studies were carried out to differentiate between the two mechanisms. The results were found to be in agreement with a free radical mechanism, with cleavage of the formal C—O linkage as the preferred mode of initiation. The overall activation energy for the decomposition was found to be 190 kJ mol-1.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 1985-1996 
    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: Polymers prepared by curing thiol-terminated liquid polysulfide polymer [HS(RS2)nRSH, R = —CH2CH2OCH2OCH2CH2—] with p-quinonedioxime, PbO2, and MnO2 were studied by pyrolysis-GC and thermogravimetry. Characteristic differences were observed in the composition of the pyrolyzates under flash pyrolysis at 420 and 470°C. The concentration of the cyclic monomer, 1,3-dioxa-6,7-dithionane, in the pyrolyzates was found to vary considerably from polymer to polymer. The change in mechanism with the extent of degradation and the corresponding overall activation energies were evaluated by thermogravimetry. The pyrolysis-GC and thermogravimetric data were shown to provide partial characterization of the substrates. Mn appears to be in a coordinated complex in the MnO2-cured polymer.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1007-1017 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photo-initiated oligomerization of bromotrifluoroethylene in chlorotrifluoromethane medium was found to yield a complex mixture of products. 19F-nmr, infrared and GC-MS spectra revealed the presence of -CF2Br and  - CF = CF2 and the absence of  - CF Br2 and  - CF3 end groups in the products. Oligomers up to pentamers were identified and their structures elucidated by GC-MS. A plausible mechanism for their formation is suggested.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2251-2263 
    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: Thermal degradation of functionally terminated liquid polybutadiene polymers, carboxy-terminated polybutadiene (CTPB), hydroxy-terminated polybutadiene (HTPB), and poly(butadieneacrylonitrile-acrylic acid) terpolymer (PBAN) and their cured analogues were studied by pyrolysis gas chromatography in the temperature range 500-850°C. It was found that CTPB, HTPB, and PBAN could be distinguished from one another by the variation in the composition of their pyrolyzates. The differences in the product composition were rationalized by the relative importance of unzipping and hydrogen transfer reactions in the mechanisms of their degradation. The presence of the OH group was found to favor hydrogen transfer reactions whereas the COOH group has only marginal effect. The cyclization reactions were found to predominate in the thermal degradation of cured PBAN and the pyrolysis results were substantiated by thermogravimetric studies at several heating rates. The activation energy for the decomposition of cured PBAN was estimated to be 259 ± 16 kJ mol-1 by Ozawa's method.
    Additional Material: 3 Ill.
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  • 5
    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: 13C-NMR spectroscopy (22.5 MHz) was used to characterize poly(butadiene (B)-acrylonitrile (A)-methacrylic acid (M)) liquid terpolymers prepared by emulsion polymerization. The sequence distribution of the monomers in the terpolymers was described in terms of triads BBB, ABA, ABB, BBA, MBB, and AMB and was found to vary with the mode of addition of methacrylic acid monomer. The NMR data was found to be in good agreement with a mechanism of polymerization in which methacrylic acid is preferentially involved in initiation reactions by a thiyl radical arising from the reaction of the chain modifier, 1-dodecanethiol, and cyanoisopropyl radical generated from AIBN initiator. Binders obtained by curing the liquid terpolymers with an epoxy resin showed widely varying mechanical properties with tensile strength varying from 4.3 to 0.6 kg/cm2 and elongation at break from 130 to 450%. It was found that tensile strength increases and elongation decreases with the number of acrylonitrile units between the methacrylic acid crosslinks. Good correlation was obtained between triad population ratio [ABB + BBA] [BBvB]/[ABA][MBB] and the mechanical properties of the binders. Pyrolysis-GC data at 550 and 600°C confirmed the results obtained from 13C-NMR, and the mole ratio of butadiene to arylonitrile in the pyrolyzates showed correlation with the properties of binders.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 23 (1985), S. 475-477 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Propellants, Explosives, Pyrotechnics 20 (1995), S. 32-35 
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Thermo-oxidative degradation of hydroxy-terminated polybutadiene (HTPB) and poly(butadiene-acrylonitrile-acrylic acid) terpolymer (PBAN) binders was studied in the presence of varying amounts of ammonium perchlorate (AP). It was found that the effect of AP on the nature and composition of the pyrolyzates was similar to the effect of increase in pyrolysis temperature. Activation energy for thermal degradation was found to be about 52 kJ/mol for both the polymers. The results are discussed in terms of a linear pyrolysis model.
    Additional Material: 2 Ill.
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