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溶胶-凝胶法制备的硫酸锆显著提高山梨醇催化脱水制异山梨醇的性能:定量结构-反应性研究

Markedly Improved Catalytic Dehydration of Sorbitol to Isosorbide by Sol-Gel Sulfated Zirconia: A Quantitative Structure-Reactivity Study.

作者信息

Hopper Jack T, Ma Ruining, Rawlings James B, Ford Peter C, Abu-Omar Mahdi M

机构信息

Department of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.

Department of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.

出版信息

ACS Catal. 2023 Jul 19;13(15):10137-10152. doi: 10.1021/acscatal.3c00755. eCollection 2023 Aug 4.

Abstract

Isosorbide, a bicyclic C6 diol, has considerable value as a precursor for the production of bio-derived polymers. Current production of isosorbide from sorbitol utilizes homogeneous acid, commonly HSO, creating harmful waste and complicating separation. Thus, a heterogeneous acid catalyst capable of producing isosorbide from sorbitol in high yield under mild conditions would be desirable. Reported here is a quantitative investigation of the liquid-phase dehydration of neat sorbitol over sulfated zirconia (SZ) solid acid catalysts produced via sol-gel synthesis. The catalyst preparation allows for precise surface area control (morphology) and tunable catalytic activity. The S/Zr ratio (0.1-2.0) and calcination temperature (425-625 °C) were varied to evaluate their effects on morphology, acidity, and reaction kinetics and, as a result, to optimize the catalytic system for this transformation. With the optimal SZ catalyst, complete conversion of sorbitol occurred in <2 h under mild conditions to give isosorbide in 76% yield. Overall, the quantitative kinetics and structure-reactivity studies provided valuable insights into the parameters that govern product yields and SZ catalyst activity, central among these being the relative proportion of acid site types and Brønsted surface density.

摘要

异山梨醇,一种双环C6二醇,作为生物基聚合物生产的前体具有相当大的价值。目前由山梨醇生产异山梨醇采用均相酸,通常是硫酸,会产生有害废物并使分离复杂化。因此,需要一种能够在温和条件下由山梨醇高产率生产异山梨醇的多相酸催化剂。本文报道了通过溶胶-凝胶合成法制备的硫酸化氧化锆(SZ)固体酸催化剂上纯山梨醇的液相脱水定量研究。催化剂的制备允许精确控制表面积(形态)和可调的催化活性。改变S/Zr比(0.1 - 2.0)和煅烧温度(425 - 625℃)以评估它们对形态、酸度和反应动力学的影响,从而优化该转化反应的催化体系。使用最佳的SZ催化剂,山梨醇在温和条件下不到2小时即可完全转化,异山梨醇产率为76%。总体而言,定量动力学和结构-反应性研究为控制产物产率和SZ催化剂活性的参数提供了有价值的见解,其中核心是酸位点类型的相对比例和布朗斯特表面密度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28f9/10411504/5d38d390c174/cs3c00755_0013.jpg

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