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以植物油衍生的环氧化物HWO@Al-MCM-41作为可循环催化剂在室温下制备生物基醛类

Room-temperature production of bio-based aldehydes from vegetable oil-derived epoxide HWO@Al-MCM-41 as recyclable catalyst.

作者信息

Peng Libo, Xie Qinglong, Nie Yong, Liu Xuejun, Lu Meizhen, Ji Jianbing

机构信息

Institute of Chemical Engineering, Zhejiang University of Technology, Zhejiang Province Key Laboratory of Biofuel, Biodiesel Laboratory of China Petroleum and Chemical Industry Federation No. 18 Chaowang Road Hangzhou Zhejiang 310014 China

出版信息

RSC Adv. 2019 Jul 25;9(40):23061-23070. doi: 10.1039/c9ra04348a. eCollection 2019 Jul 23.

Abstract

The oxidative cleavage of vegetable oils and their derivatives to produce bio-based aldehydes is a potentially useful process, although the aldehyde products are readily oxidized to carboxylic acids and thus seldom obtained in high yields. The present study developed a room-temperature method for the synthesis of bio-aldehydes the oxidative cleavage of vegetable oil-derived epoxides, using HWO as the catalyst, HO as the oxidant, and -BuOH as the solvent. Reactions were carried out at temperatures ranging from 25 to 35 °C for 3.5-10.5 h, and provided >99% conversion and >90% aldehyde yield. In particular, an approximately 97% yield was obtained at 25 °C after 10.5 h. As the reaction proceeded, the HWO dissolved to form a W-containing anion. Several mesoporous Al-MCM-41 materials having different Si/Al ratios were hydrothermally synthesized and used as adsorbents to recover the catalyst by adsorbing these anions. The adsorption capacity of the Al-MCM-41 was found to increase with decreases in the Si/Al ratio. The Al-MCM-41 had little effect on the oxidative cleavage reaction at 25 °C, and thus could be directly added to the reaction system. The excellent anion adsorption performance of the Al-MCM-41 greatly improved the reusability of the HWO catalyst. When using the Al-MCM-41 with the best adsorption performance, there was no significant decrease in the activity of the catalyst following five reuses.

摘要

将植物油及其衍生物进行氧化裂解以生产生物基醛是一个潜在有用的过程,尽管醛产物很容易被氧化成羧酸,因此很少能获得高产率。本研究开发了一种室温方法来合成生物醛——以植物油衍生的环氧化物为原料进行氧化裂解,使用HWO作为催化剂,HO作为氧化剂,-BuOH作为溶剂。反应在25至35°C的温度下进行3.5 - 10.5小时,转化率>99%,醛产率>90%。特别是在25°C下反应10.5小时后,产率约为97%。随着反应进行,HWO溶解形成含W的阴离子。水热合成了几种具有不同Si/Al比的介孔Al-MCM-41材料,并用作吸附剂,通过吸附这些阴离子来回收催化剂。发现Al-MCM-41的吸附容量随着Si/Al比的降低而增加。Al-MCM-41在25°C下对氧化裂解反应影响很小,因此可以直接添加到反应体系中。Al-MCM-41出色的阴离子吸附性能大大提高了HWO催化剂的可重复使用性。使用吸附性能最佳的Al-MCM-41时,催化剂在五次重复使用后活性没有显著下降。

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