Difference in the stability of network between natural rubber and polyisoprene vulcanizates

被引:0
|
作者
Ito, Masayoshi [1 ]
Takizawa, Ayaka [1 ]
机构
[1] Tokyo Univ Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, Japan
来源
KGK-KAUTSCHUK GUMMI KUNSTSTOFFE | 2012年 / 65卷 / 04期
关键词
Natural rubber; polyisoprene; ESR; stability of network; inhomogeneous network; STRAIN-INDUCED CRYSTALLIZATION; X-RAY-SCATTERING; ALPHA-TERMINAL GROUP; SILICA-FILLED SBR; STRUCTURAL-CHARACTERIZATION; RUBBER/FILLER INTERACTIONS; ULTRAVIOLET IRRADIATION; BRANCH-POINTS; FREE RADICALS; ESR;
D O I
暂无
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Stability of network against the mechanical stress during stretching was evaluated from the in-situ ESR measurements during stretching for vulcanized natural rubber (NR) and polyisoprene (IR). Large amounts of unpaired electrons (free radicals) were produced during stretching of vulcanized NR. However, the amounts were less in vulcanized IR. That is, the stability of network against the mechanical stress was lower for NR than for IR. Combined these results with the data for deproteinized natural rubber, the low stability of network structure in NR was explained by the inhomogeneous network which was formed by hydrogen bond at terminal groups of NR and by sulfur linkages, in addition to the inhomogeneous vulcanization induced by protein in NR. The explanation was supported by the results of permanent set for the vulcanized samples.
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页码:24 / 27
页数:4
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