

FOLLOWUS
a.School of Materials Science and Engineering, Hainan University, Haikou 570228, China
b.Hainan Advanced Natural Rubber Composite Materials Engineering Research Center Co., Ltd., Chengmai 571924, China
dingaw@163.com (A.W.D.)
mchluo@hainanu.edu.cn (M.C.L.)
Received:03 April 2026,
Revised:2026-04-29,
Accepted:06 May 2026,
Online First:22 August 2026,
Published:2026-06
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Wu, Z. L.; Li, L. R.; Zhou, Y.; Yang, D.; Liao, S. Q.; Mei, J. F.; Ding, A. W.; Luo, M. C. Exchange kinetics of reprocessable vulcanization networks regulated by inverse vulcanization copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3740-4
Zhou-Liang Wu, Ling-Rui Li, Yu Zhou, et al. Exchange Kinetics of Reprocessable Vulcanization Networks Regulated by Inverse Vulcanization Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9.
Wu, Z. L.; Li, L. R.; Zhou, Y.; Yang, D.; Liao, S. Q.; Mei, J. F.; Ding, A. W.; Luo, M. C. Exchange kinetics of reprocessable vulcanization networks regulated by inverse vulcanization copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3740-4 DOI:
Zhou-Liang Wu, Ling-Rui Li, Yu Zhou, et al. Exchange Kinetics of Reprocessable Vulcanization Networks Regulated by Inverse Vulcanization Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9. DOI: 10.1007/s10118-026-3740-4.
The reprocessing and recycling of vulcanized rubbers remain challenging because conventional vulcanization networks are irreversible. Here
we designed a modified sulfur crosslinker
via
inverse vulcanization to regulate the exchange kinetics of vulcanization networks
thereby governing the mechanical recovery behavior of reprocessed rubbers. Copolymers of sulfur and thioctic acid (CSTA)
synthesized
via
inverse vulcanization
were employed to crosslink butadiene-styrene rubber. After vulcanization
thioctic acid (TA) introduces dynamic disulfide bonds into the conventional vulcanization networks
enabling thermally activated network rearrangement while preserving the overall crosslinked structure. Kinetic analysis revealed that increasing the TA content accelerated network exchange and significantly lowered the apparent activation energy for network rearrangements. Correspondingly
the recovery of the mechanical properties after reprocessing improved with increasing TA content. These results establish a clear correlation between vulcanization network exchange kinetics and macroscopic mechanical performance
providing a kinetic basis for the design of reprocessable vulcanization networks and offering a promising route toward recyclable high-performance rubber materials.
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