Solvent-Free Depolymerization of Plastic Waste Enabled by Plastic-Catalyst Interfacial Engineering

被引:10
作者
Bai, Xiaoshen [1 ]
Aireddy, Divakar R. [1 ]
Roy, Amitava [2 ]
Ding, Kunlun [1 ]
机构
[1] Louisiana State Univ, Dept Chem Engn, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr Adv Microstruct & Devices, Baton Rouge, LA 70806 USA
关键词
Contact Mass; Depolymerization; Interfacial Engineering; Polyethylene Terephthalate; Solvent-Free; DIMETHYL TEREPHTHALATE; POLYETHYLENE; ETHYLENE;
D O I
10.1002/anie.202309949
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Depolymerization of condensation polymers by chemolysis often suffers from the large usage of solvents and homogeneous catalysts such as acids, bases, and metal salts. The catalytic efficiency of heterogeneous catalysts is largely constrained by the poor interfacial contact between solid catalysts and solid plastics below melting points. We report here our discovery of autogenous heterogeneous catalyst layer on polyethylene terephthalate surfaces during the generally believed homogeneous catalytic depolymerization process. Inspired by the "contact mass" concept in industrial chlorosilane production, we further demonstrate that the construction of plastic-catalyst solid-solid interfaces enables solvent-free depolymerization of polyethylene terephthalate by vapor phase methanolysis at relatively low temperatures. Trace amounts of earth-abundant element (zinc) introduced by electrostatic adsorption is sufficient for catalyzing the depolymerization. The concept of plastic-catalyst contact mass interfacial catalysis might inspire new pathways for tackling plastic waste problems.
引用
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页数:7
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