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决定沸石在热液态水中稳定性的因素。

Factors that Determine Zeolite Stability in Hot Liquid Water.

机构信息

School of Chemical, Biological and Materials Engineering, University of Oklahoma , 100 East Boyd Street, Norman, Oklahoma 73019, United States.

Center for Interfacial Reaction Engineering (CIRE), University of Oklahoma , 100 East Boyd Street, Norman, Oklahoma 73019, United States.

出版信息

J Am Chem Soc. 2015 Sep 16;137(36):11810-9. doi: 10.1021/jacs.5b07398. Epub 2015 Sep 1.

Abstract

The susceptibility of zeolites to hot liquid water may hamper their full utilization in aqueous phase processes, such as those involved in biomass conversion and upgrading reactions. Interactions of zeolites with water strongly depend on the presence of hydrophilic moieties including Brønsted acid sites (BAS), extraframework cations, and silanol defects, which facilitate wetting of the surface. However, it is not clear which of these moieties are responsible for the susceptibility of zeolites to liquid water. Previous studies have offered contradictory explanations because the role of each of these characteristics has not been investigated independently. In this work, a systematic comparison has been attempted by relating crystallinity losses to the variation of each of the five zeolite characteristics that may influence their stability in liquid water, including number of BAS, Si-O-Si bonds, framework type, silanol defects, and extraframework Al. In this study, we have systematically monitored the crystallinity changes of a series of HY, H-ZSM-5, and H-β zeolite samples with varying Si/Al ratio, density of BAS, zeolite structure, and density of silanol defects upon exposure to liquid water at 200 °C. The results of this comparison unambiguously indicate that the density of silanol defects plays the most crucial role in determining susceptibility of zeolites to hot liquid water. By functionalizing the silanol defects with organosilanes, the hydrophobicity of defective zeolite is increased and the tolerance to hot liquid water is significantly enhanced.

摘要

沸石对热液态水的敏感性可能会阻碍它们在水相过程中的充分利用,例如涉及生物质转化和升级反应的过程。沸石与水的相互作用强烈依赖于亲水性部分的存在,包括 Brønsted 酸位 (BAS)、骨架外阳离子和硅醇缺陷,这些部分有助于表面润湿。然而,目前尚不清楚这些部分中哪一个负责沸石对液态水的敏感性。先前的研究提供了相互矛盾的解释,因为这些特征中的每一个的作用都没有被独立研究。在这项工作中,通过将结晶度损失与可能影响其在液态水中稳定性的五种沸石特性中的每一种的变化相关联,尝试了系统的比较,这五种特性包括 BAS 的数量、Si-O-Si 键、骨架类型、硅醇缺陷和骨架外 Al。在这项研究中,我们系统地监测了一系列 HY、H-ZSM-5 和 H-β 沸石样品在 200°C 下暴露于液态水中时,随着 Si/Al 比、BAS 密度、沸石结构和硅醇缺陷密度的变化,结晶度的变化。这种比较的结果明确表明,硅醇缺陷的密度在确定沸石对热液态水的敏感性方面起着最重要的作用。通过用有机硅烷官能化硅醇缺陷,缺陷沸石的疏水性增加,对热液态水的耐受性显著增强。

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