化学
沸石
脱水
丙烯酸甲酯
催化作用
产量(工程)
位阻效应
离子交换
无机化学
核化学
有机化学
离子
材料科学
冶金
聚合物
生物化学
共聚物
作者
Shiyao Lu,Jian Zhang,Hao Meng,Xiaoyuan Qin,Jianbin Huang,Yehao Liang,Feng‐Shou Xiao
标识
DOI:10.1021/acssuschemeng.3c01716
摘要
Dehydration of methyl lactate (ML) obtained from biomass is a sustainable route for the production of methyl acrylate (MA). Herein, we demonstrate that cesium-exchanged Al-rich Beta zeolite (Cs-Beta) is highly efficient for the dehydration of ML to MA, exhibiting full ML conversion with 87.4% MA yield at 340 °C. In situ FT-IR spectra and kinetic studies provide evidence that the ML dehydration on the Cs-Beta zeolite follows a forward ion-exchange/dehydration/reverse ion-exchange reaction pathway. Model experiments, DFT calculations, TG-DSC analysis, and FT-IR spectra showed that coke formation competes with the dehydration of ML to MA. Kinetic studies and theoretical simulations demonstrate that cesium cations in the micropores of Beta zeolite have a strong steric hindrance, suppressing the formation of oligomers and coke. These results offer new insights for developing highly selective and stable catalysts for the dehydration of ML to MA in the future.
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