1999
DOI: 10.1016/s0141-3910(98)00114-1
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Thermal degradation of polystyrene, poly(1,4-butadiene) and copolymers of styrene and 1,4-butadiene irradiated under air or argon with 60Co-γ-rays

Abstract: This paper is NOT THE PUBLISHED VERSION; but the author's final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation below.

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Cited by 69 publications
(35 citation statements)
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“…The gel content and swelling ratio [2], [3], [4] were determined as previously described [1] . Gel content is determined by heating a sample of known mass in a solvent for 24 h. The recovered insoluble sample is then thoroughly dried at elevated temperatures under vacuum and the mass of insoluble polymer is determined.…”
Section: Characterization Of Cross-linkingmentioning
confidence: 99%
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“…The gel content and swelling ratio [2], [3], [4] were determined as previously described [1] . Gel content is determined by heating a sample of known mass in a solvent for 24 h. The recovered insoluble sample is then thoroughly dried at elevated temperatures under vacuum and the mass of insoluble polymer is determined.…”
Section: Characterization Of Cross-linkingmentioning
confidence: 99%
“…In previous work from these laboratories [1] , it has been shown that 60 Co-γ-ray irradiation will effect cross-linking of polybutadiene, PBD, but polystyrene, PS, can be cross-linked by irradiation only in the presence of oxygen. The thermal stability of 60 Co-γ-ray-irradiated PBD is lower than that of unirradiated polymer while irradiated PS has enhanced thermal stability relative to the virgin polymer.…”
Section: Introductionmentioning
confidence: 99%
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“…Some properties of SBR such as abrasive resistance, heat resistance, and aging resistance are superior to those of NR, and thus SBR has replaced NR partially in many fields. However, due to the instability of double bonds in SBR to ultraviolet, heat, and oxygen, aging processes like chain scission, chain crossing, and oxidization take place easily when the SBR products are in use just like other styrene-butadiene copolymers [9][10][11][12][13][14][15][16].…”
Section: H2o(l) + 2e⁻→ H2 (G) + 2 Oh-(a Q) ( 4 )mentioning
confidence: 99%
“…[1][2][3]. On the contrary, styrene easily copolymerizes with different monomers such as acrylonitrile, methacrylamide, divinylbenzene, butadiene, maleic anhydride, vinyl chloride, esters of organic acids, e.g., acrylates or methacrylates, unsaturated polyesters or others creating polymeric materials with unique properties suitable for many industrial applications [4][5][6][7][8][9][10][11][12][13][14].…”
Section: Introductionmentioning
confidence: 99%