催化作用
光热治疗
材料科学
聚酯纤维
聚对苯二甲酸乙二醇酯
化学工程
钴
纳米技术
废物管理
光化学
有机化学
复合材料
化学
冶金
工程类
作者
Yu Liu,Xuchun Wang,Qingye Li,Tianran Yan,Xiangxi Lou,Congyang Zhang,Muhan Cao,Liang Zhang,Tsun‐Kong Sham,Qiao Zhang,Le He,Jinxing Chen
标识
DOI:10.1002/adfm.202210283
摘要
Abstract Photothermal catalytic conversion of waste plastics into fuels and/or feedstocks using renewable solar energy can achieve solar‐to‐chemical conversion, resource sustainability, and environmental remediation simultaneously. However, the construction of photothermal catalysts with strong light absorption and high catalytic activity remains a great challenge. In this work, integrated cobalt single‐site catalysts (Co SSCs), coupled with strong photothermal conversion, high catalytic activity, and stability, are employed to catalyze the glycolysis of polyesters. The unique coordination‐unsaturated CoO 5 single‐site can coordinate with the carbonyl groups in polyester, thus boosting the nucleophilic addition elimination processes. As a result, the space‐time yield of Co SSCs is an order of magnitude higher than that of general catalysts. In addition, the polyethylene terephthalate (PET) conversion and bis(2‐hydroxyethyl) terephthalate yield in photothermal catalysis are 5.4 and 6.6 times higher than those of thermal catalysis under the same conditions, which are contributed by the localized heating effect. Technical economic analysis shows that the recycling of 10 5 tons of waste PET by photothermal catalysis consumes 146.4 GW·h electrical energy and misses 7.44 × 10 4 tons of CO 2 emission. Therefore, a high‐efficient photothermal catalytic plastic recycling system is of great significance for waste plastic valorization.
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