TY - JOUR
T1 - Upcycling of Vulcanized Rubber via Controlled Backbone Cleavage and Functionalization
AU - Sun, Zongxue
AU - Zhang, Xiaoying
AU - Wang, Xinde
AU - Song, Ningning
AU - Wang, Hongyun
AU - Guo, Zhenhao
AU - Li, Xinyao
AU - Huang, Daye
AU - Gu, Hongyi
AU - Li, Lin
AU - Li, Guangyu
AU - Tian, Jia
AU - Ju, Hao
AU - Qin, Han
AU - Hesaramiri, Maryam T.
AU - Jiang, Yijie
AU - Ding, Shengtao
AU - Chen, Jiayao
AU - Zhang, Zhen
AU - Guo, Baochun
AU - Zhang, Liqun
AU - Zhang, Wei
AU - Tian, Ming
AU - Wang, Teng
AU - Cao, Peng Fei
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/3/18
Y1 - 2026/3/18
N2 - Vulcanized rubbers, essential in tires and many other elastomers, are exceptionally difficult to recycle because their sulfur-cross-linked, additive-rich networks resist chemical degradation. This high resistance has created a mounting environmental burden, yet strategies that operate under mild and nontoxic-gas-emitting conditions while producing valuable products remain scarce. Here we report a mild, one-step oxidative approach that selectively cleaves backbone C═C bonds in both thermoplastic and vulcanized rubbers. By regulating the phase of an N-hydroxyphthalimide (NHPI)-based catalytic system, the process yields functionalized fragments with high terminal-group selectivity and tunable molar masses, following distinct degradation kinetics that afford tunable, time-independent molar masses. These chemically functionalized fragments can be directly reused for applications such as 3D printing and adhesives or replace raw rubbers and plasticizers in tire tread formulations. This method has also been successfully applied to the recycling of real-life rubber waste, including tires and gloves, achieving >95% recovery, thus providing a practically useful and scalable route for chemical upcycling of highly inert polymer waste.
AB - Vulcanized rubbers, essential in tires and many other elastomers, are exceptionally difficult to recycle because their sulfur-cross-linked, additive-rich networks resist chemical degradation. This high resistance has created a mounting environmental burden, yet strategies that operate under mild and nontoxic-gas-emitting conditions while producing valuable products remain scarce. Here we report a mild, one-step oxidative approach that selectively cleaves backbone C═C bonds in both thermoplastic and vulcanized rubbers. By regulating the phase of an N-hydroxyphthalimide (NHPI)-based catalytic system, the process yields functionalized fragments with high terminal-group selectivity and tunable molar masses, following distinct degradation kinetics that afford tunable, time-independent molar masses. These chemically functionalized fragments can be directly reused for applications such as 3D printing and adhesives or replace raw rubbers and plasticizers in tire tread formulations. This method has also been successfully applied to the recycling of real-life rubber waste, including tires and gloves, achieving >95% recovery, thus providing a practically useful and scalable route for chemical upcycling of highly inert polymer waste.
UR - https://www.scopus.com/pages/publications/105033075264
U2 - 10.1021/jacs.5c20016
DO - 10.1021/jacs.5c20016
M3 - 文章
C2 - 41771774
AN - SCOPUS:105033075264
SN - 0002-7863
VL - 148
SP - 10640
EP - 10648
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 10
ER -