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Cyclodehydration of 14-butanediol over Zr-Al Catalysts: Effect of Reaction Medium

机译:Zr-Al催化剂上14-丁二醇的环脱水作用:反应介质的影响

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摘要

The conversion of 1,4-butanediol (BDO) to tetrahydrofuran (THF) in aqueous phase is desirable because BDO production technology is shifting to bio-based aqueous fermentation routes. In this study, liquid-phase cyclodehydration of BDO to THF was studied in two reaction media (pure BDO and aqueous BDO feeds) at 200–240 °C using ZrO2-Al2O3 (ZA) mixed oxides, which were made with a co-precipitation method and were characterized with XRD, BET, SEM/EDX, pyridine and n-butylamine adsorptions. The maximum acidity and the largest surface area occurred at Zr/Al atomic ratios of 1/1 (ZA11) and 1/3 (ZA13), respectively. The reaction exhibited pseudo-first-order; aqueous BDO feed had much greater rate constant than pure BDO feed, ascribed to the acidic properties of adsorbed water molecules (coordinated to surface metal cations) for the former case. For pure BDO feed, linear relation was observed between rate constant and catalyst acidity, and ZA11 reached a THF yield of 90.1% at 240 °C. With aqueous BDO feed, rate constant increased linearly with increasing surface area and ZA13 reached a THF yield of 97.1% at 220 °C. The change of optimum catalyst composition with reaction medium suggests that active sites for catalyzing BDO cyclodehydration changed with the reaction environment.
机译:在水相中将1,4-丁二醇(BDO)转化为四氢呋喃(THF)是理想的,因为BDO生产技术正在转向基于生物的水性发酵路线。在这项研究中,研究了在200–240°C下使用ZrO2-Al2O3(ZA)混合氧化物在两种反应介质(纯BDO和水性BDO进料)中将BDO液相环化为THF的方法,这些氧化物是通过共沉淀法制备的用XRD,BET,SEM / EDX,吡啶和正丁胺吸附进行表征。最大酸度和最大表面积分别在Zr / Al原子比为1/1(ZA11)和1/3(ZA13)时出现。反应表现出伪一级。水性BDO进料的速率常数比纯BDO进料大得多,这归因于前一种情况下吸附水分子(与表面金属阳离子配位)的酸性。对于纯BDO进料,观察到速率常数与催化剂酸度之间存在线性关系,并且ZA11在240°C下的THF收率达到90.1%。对于含水的BDO进料,速率常数随表面积的增加而线性增加,并且ZA13在220°C时的THF收率为97.1%。反应介质的最佳催化剂组成的变化表明,催化BDO环脱水反应的活性中心随反应环境的变化而变化。

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