催化作用
产量(工程)
肿胀 的
降级(电信)
热稳定性
材料科学
化学工程
多金属氧酸盐
化学
核化学
复合材料
有机化学
计算机科学
电信
工程类
作者
Pengtao Fang,Shuqian Xia,Xingmei Lü
标识
DOI:10.1016/j.jece.2022.107823
摘要
The development of catalysts with high thermal stability, high catalytic activity and high cycling performance has been an important challenge in PET alcoholysis research. PET degradation is a surface interface controlled process, but PET as a dense solid with lower specific surface area severely reduces its degradation rate. Here, the high specific surface area (0.4–3.3 m2/g) and the large number of pores (0–17.5 nm) formed by the swelling of PET at high temperature were used to break the interfacial confinement between the reactants; then the rapid and complete degradation of PET was achieved under the multi-hydrogen bonding microenvironment formed by the multi-active site polyoxometalate (POM) catalysts K10[M4(H2O)2(PW9O34)2]-H2O (M = Zn, Mn, Cu, Ni, Co) and EG. Finally, accompanied by the attack of the transition metal active site on CO of PET, 1.0 g of PET could be completely degraded in 5 min under the optimal reaction conditions (2.0 wt% of catalyst to PET, 240 °C) and the bis(hydroxyethyl) terephthalate (BHET) yield of 92.8% was achieved within 8 min. Moreover, the catalyst could be recycled more than 30 times, which is very meaningful. In the same time, the mechanism of PET alcoholysis was investigated and proposed a mechanism of PET alcoholysis.
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