Depolymerization of polyethyleneterephthalate in supercritical methanol

被引:61
作者
Kim, BK [1 ]
Hwang, GC [1 ]
Bae, SY [1 ]
Yi, SC [1 ]
Kumazawa, H [1 ]
机构
[1] Hanyang Univ, Dept Chem Engn, Kyunggi Do 425791, Ansan, South Korea
关键词
depolymerization; polyethyleneterephthalate; supercritical methanol; methanolysis;
D O I
10.1002/app.1645.abs
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The depolymerization of polyethyleneterephthalate (PET) in supercritical methanol was carried out using a batch-type autoclave reactor. The total conversion and the yield of dimethylterephthalate (DMT) increased with rising temperature. The final yield of DMT at 300 degreesC and 310 degreesC reached 97.0% and 97.7%, respectively. The yield of DMT was markedly increased when the methanol density was 0.08 g/cm(3), and leveled off at higher densities. A kinetic model to describe the depolymerization of PET in supercritical methanol was proposed, where the scission of one ester linkage in PET by a methanol molecule produces one carboxymethyl group and one hydroxyl group. The values of the forward reaction rate constant at different temperatures were determined by comparing the observed time dependence of carboxymethyl group concentration with that calculated by the proposed model. The activation energy was evaluated to be 49.9 kJ/mol, a value close to a Literature value (55.7 kJ/mol). (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:2102 / 2108
页数:7
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