Study on the Ultimate Fracture Properties and Failures of Polymer Materials( I )Kinetic Model Theory of Tensile Strength for Polymer Networks with Constant Extension Rate
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Study on the Ultimate Fracture Properties and Failures of Polymer Materials( I )Kinetic Model Theory of Tensile Strength for Polymer Networks with Constant Extension Rate
CIESC JournalIssue 2, (1990)
作者机构:
北京化工学院高分子材料研究所,中国科技大学应用化学系 ,合肥,北京
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Online First:25 April 1990,
Published:25 April 1990
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宋名实, 张焕芝. Study on the Ultimate Fracture Properties and Failures of Polymer Materials( I )Kinetic Model Theory of Tensile Strength for Polymer Networks with Constant Extension Rate[J]. CIESC Journal, 1990, (2).
DOI:
宋名实, 张焕芝. Study on the Ultimate Fracture Properties and Failures of Polymer Materials( I )Kinetic Model Theory of Tensile Strength for Polymer Networks with Constant Extension Rate[J]. CIESC Journal, 1990, (2).DOI:
Study on the Ultimate Fracture Properties and Failures of Polymer Materials( I )Kinetic Model Theory of Tensile Strength for Polymer Networks with Constant Extension Rate
A new kinetic theory of tensile strength for polymer networks has been proposed. It is based on the Eyring chemical activation rate theory and the molecular theory of rubber elasticity at large deformations. The coefficient of overstress of a polymer chain is derived by combining the deformation behavior
stress concentration of a polymer chain and the chain orientation as a united event of polymer failure. A kinetic equation for bond rupture of over-stressed chain is established by taking the coefficient of overstress as a variable. After integration and simplification a new equation of state for ultimate fracture is obtained. It is successful in reating the ultimate strength and extensibility to the parameters of structure
the temperature and the extension rate. The failures of four different polymer networks were studied by uniaxial extension method. These experimental data of ultimate properties were treated with the proposed theory. The results show that the proposed theory can predict the failure behavior of polymer networks and provide a theoretical foundation for the construction of failure envelop.