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Determination of residual levels of unsaturation in partially hydrogenated poly(2,3-diphenyl-1,3-butadiene) using thermogravimetry
Institution:1. Shanxi Key Laboratory of Ecological Animal Science and Environmental Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi 030801, People’s Republic of China;2. Department of Biology, Taiyuan Normal University (TYNU), Taiyuan 030031, People’s Republic of China;3. College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, Henan 471003, People’s Republic of China;1. Institute of Hydrocarbon Processing SB RAS, Neftezavodskaya St., 54, Omsk, 644040, Russian Federation;2. Boreskov Institute of Catalysis SB RAS, Pr. Ac. Lavrentieva, 5, Novosibirsk, 630090, Russian Federation;3. National Research Tomsk Polytechnic University, Lenin Av., 30, Tomsk, 634050, Russian Federation;1. Food Science and Human Nutrition Department, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL 32611, United States;2. Agricultural and Biological Engineering Department, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL 32611, United States;3. School of Food Science and Technology, Jiangnan University, Jiangsu 214122, China;1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Soochow University, 199 Renai Street, Suzhou, Jiangsu 215123, China;2. Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
Abstract:The thermal degradation characteristics of head-to-head poly(styrene) (HHPS) should provide insight with respect to the impact of head-to-head placement on the thermal stability of the traditional atactic head-to-tail polymer (HTPS). The synthesis of head-to-head poly(styrene) must be accomplished indirectly. The HHPS is most satisfactorily obtained by dissolving metal reduction of poly(2,3-diphenyl-1,3-butadiene) (PDBD) generated by radical polymerization of the corresponding diene monomer. Full saturation of the polymer mainchain requires several iterations of the reduction procedure. Since the decomposition of PDBD is prominent at 374 °C and that for HHPS is similarly facile at 406 °C, it seemed feasible that TGA of partially hydrogenated PDBD might be utilized as a convenient means of monitoring the extent of hydrogenation. This has been demonstrated for various levels of unsaturation remaining—from approximately 90 to less than 10%. Within this range the peak areas from the DTG plots of the partially hydrogenated polymer provide a good reflection of the ratio of unsaturated to saturated units in the polymer. Even low levels of unsaturation in the polymer may be detected by the asymmetry of the decomposition peak for the polymer.
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