TS-1 与原位合成 H2O2 的选择性氧化作用

IF 6.3 3区 综合性期刊 Q1 Multidisciplinary Fundamental Research Pub Date : 2026-03-01 Epub Date: 2024-04-10 DOI:10.1016/j.fmre.2024.03.023
Dong Lin , Richard J. Lewis , Xiang Feng , Graham J. Hutchings
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引用次数: 0

摘要

与好氧途径或其他化学计量氧化剂相比,预先形成的H2O2与钛硅酸盐共型相结合的原料增值特别有吸引力,因为它具有更高的选择性、更低的操作温度和更高的工艺效率(特别是更低的能耗和更高的原子经济性)。然而,与商用H2O2应用相关的许多环境和财务问题仍然存在。这些问题使得人们对原位合成氧化剂在一系列化学转化中的应用越来越感兴趣。在此,我们概述了这一新兴氧化催化领域的关键贡献,特别关注丙烯环氧化和酮氨肟化,这是目前两个关键的工业规模工艺,利用预成型H2O2和钛硅酸盐催化剂TS-1进行化学合成。这一贡献将突出原位h2o2介导的原料升级的潜力,以取代现有技术,并有助于化学合成部门宣布的可持续发展目标。
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Selective oxidation by TS-1 coupled with in-situ synthesised H2O2
Feedstock valorisation with preformed H2O2 in conjunction with titanosilicate zeotypes is particularly attractive due to the increased selectivity, lower operating temperatures and improved process efficiency (particularly lower energy usage and enhanced atom economy) compared to aerobic pathways or alternative stoichiometric oxidants. However, numerous environmental and financial concerns associated with the application of commercial H2O2 remain. These concerns have led to a growing interest in the application of the in-situ synthesized oxidant for a range of chemical transformations. Herein, we provide an overview of the key contributions to this emerging field of oxidative catalysis, with a particular focus on propene epoxidation and ketone ammoximation, which are currently two crucial industrial-scale processes that utilise preformed H2O2 with the titanosilicate catalyst TS-1 for chemical synthesis. This contribution will highlight the potential for in-situ H2O2-mediated feedstock upgrading to replace existing technologies and contribute to the declared sustainability goals of the chemical synthesis sector.
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来源期刊
Fundamental Research
Fundamental Research Multidisciplinary-Multidisciplinary
CiteScore
4.00
自引率
1.60%
发文量
294
审稿时长
79 days
期刊介绍:
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