硫化
化学
弹性体
聚合物
天然橡胶
热塑性塑料
表面改性
惰性
热塑性弹性体
化学改性
高分子化学
化学工程
固化(化学)
增塑剂
胶粘剂
低聚物
摩尔质量
共聚物
丁基橡胶
催化作用
耐化学性
有机化学
抵抗
化学结构
选择性
降级(电信)
相(物质)
键裂
漆
涂层
原材料
踩
作者
Zongxue Sun,Xiaoying Zhang,xinde wang,Ningning Song,Hao Wang,Zhenhao Guo,Xinyao Li,Daye Huang,Hao Gu,Lin Li,Guangyu Li,Jia Tian,Hao Ju,Han Qin,Maryam Tajik HesarAmiri,Yijie Jiang,Shengtao Ding,J. C. Chen,Zhen Zhang,Baochun Guo
摘要
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.
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