FN Archimer Export Format PT J TI Strain-induced crystallization in an unfilled polychloroprene rubber: Kinetics and mechanical cycling BT AF LE GAC, Pierre-Yves ALBOUY, Pierre-Antoine PETERMANN, Denis AS 1:1;2:2;3:2; FF 1:PDG-REM-RDT-LCSM;2:;3:; C1 IFREMER Ctr Bretagne, Marine Struct Lab, BP70, F-29280 Plouzane, France. Univ Paris Saclay, Univ Paris Sud, CNRS, Lab Phys Solides, F-91405 Orsay, France. C2 IFREMER, FRANCE UNIV PARIS SACLAY, FRANCE SI BREST SE PDG-REM-RDT-LCSM IN WOS Ifremer jusqu'en 2018 copubli-france copubli-univ-france IF 3.771 TC 29 UR https://archimer.ifremer.fr/doc/00433/54467/55842.pdf LA English DT Article DE ;Polychloroprene;Strain-induced crystallization;X-ray AB 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. PY 2018 PD APR SO Polymer SN 0032-3861 PU Elsevier Sci Ltd VL 142 UT 000430358900022 BP 209 EP 217 DI 10.1016/j.polymer.2018.03.034 ID 54467 ER EF