乳酸
沸石
杂原子
密度泛函理论
基质(水族馆)
化学
丙交酯
吉布斯自由能
反应速率
物理化学
催化作用
有机化学
无机化学
计算化学
细菌
热力学
共聚物
生物
戒指(化学)
地质学
物理
聚合物
海洋学
遗传学
作者
Yunlong Xu,Linlin Yang,Chunying Si,Shuoqi Zhang,Quanxing Zhang,Guixiang Zeng,Wei Jiang
标识
DOI:10.1021/acs.iecr.2c03390
摘要
Sn-beta zeolite is a promising catalyst for the direct synthesis of lactide from lactic acid; here, we clarify the relationship between its local structure and activity through the interplay of experiments and DFT calculations. The open sites (HO-Sn-(OSi)3 with adjacent Si–OH) play a key role in the high activity of Sn-beta zeolite, where the reaction rate significantly decreases from 0.2258 mmol min–1 gcat–1 to 0.0724 mmol min–1 gcat–1 if the open sites were masked with Na+. Density functional theory (DFT) calculations show that the decrease in reaction rate comes from the weaker interaction between substrate and the open Sn site by Na+ exchange, which leads to the significant increase in the Gibbs energy barrier from 34.0 kcal/mol to 57.2 kcal/mol (rate-determining step). Other activities of heteroatom M-beta zeolites (where M = Ti, Zr, Hf) were also investigated, where the open sites were found to be crucial for the high activity in the direct synthesis of lactide as well. The information provided by this work is valuable for precise design of efficient catalysts for the one-step synthesis of lactide.
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