Strain-induced crystallization in an unfilled polychloroprene rubber: Kinetics and mechanical cycling

被引:33
作者
Le Gac, Pierre-Yves [1 ]
Albouy, Pierre-Antoine [2 ]
Petermann, Denis [2 ]
机构
[1] IFREMER, Ctr Bretagne, Marine Struct Lab, BP70, F-29280 Plouzane, France
[2] Univ Paris Saclay, Univ Paris Sud, CNRS, Lab Phys Solides, F-91405 Orsay, France
关键词
Polychloroprene; Strain-induced crystallization; X-ray; ANGLE X-RAY; VULCANIZED NATURAL-RUBBER; MOLECULAR-ORIENTATION; SYNTHETIC CIS-1,4-POLYISOPRENE; DIFFRACTION; STRESS; CRYSTAL; TEMPERATURE; POLYMERS; BEHAVIOR;
D O I
10.1016/j.polymer.2018.03.034
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polychloroprene rubber is often quoted as an example of strain-crystallizing elastomer; however, this fundamental property, known to impart good mechanical properties and fatigue resistance, has received much less attention in this class of compounds than natural rubber. The present paper relates systematic investigations combining mechanical and X-ray diffraction measurements. Crystallization kinetics are first investigated based on tensile impact tests. An approximately logarithmic time-dependence is found for the crystalline content and the time-constants are estimated at various temperatures. The impact of strain-induced crystallization on stress-strain curves under mechanical cycling conditions is further assessed. It is demonstrated that one main effect of strain-induced crystallization is a partial relaxation of the strain experienced by the amorphous fraction, although stress-hardening is simultaneously observed. Based on the stress-optical law, the contribution of the amorphous phase to the stress is shown to level off after crystallization onset, and stress-hardening is attributed to crystallite networking. The crystallite network rapidly disintegrates at the beginning of recovery, and the stress-optical law shows that the amorphous fraction becomes the only contributor to the stress at still non-negligible crystalline contents. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:209 / 217
页数:9
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