Homogeneous catalytic hydrogenation of CO2 – amino acid-based capture and utilization

IF 40.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yong Peng, Elisabetta Alberico, Henrik Junge, Matthias Beller
{"title":"Homogeneous catalytic hydrogenation of CO2 – amino acid-based capture and utilization","authors":"Yong Peng, Elisabetta Alberico, Henrik Junge, Matthias Beller","doi":"10.1039/d5cs00186b","DOIUrl":null,"url":null,"abstract":"In this review, we provide an overview of research efforts to integrate carbon dioxide capture specifically using amino acid-based sorbents with its thermocatalytic hydrogenation promoted by homogeneous metal complexes. Carbon capture and utilization (CCU) is a promising strategy for the production of fuels, chemicals and materials using CO<small><sub>2</sub></small> scrubbed from point sources and the atmosphere as a C1 feedstock while mitigating CO<small><sub>2</sub></small> emissions. Compared to established (alkanol)amines, amino acids offer some advantages as CO<small><sub>2</sub></small> capture agents due to their lower volatility, higher oxygen stability and lower regeneration energies. We report how the structural diversity of amino acids and the possibility of combining them with cations in salts and ionic liquids have been exploited in the design of absorbers for improved absorption kinetics and capacity. Furthermore, we discuss selected examples from the literature illustrating the use of 1°/2° (poly)amines, since the 1°/2° amino groups are mainly responsible for CO<small><sub>2</sub></small> chemisorption in amino acid-based capture media, the nature of the corresponding adducts, and the most promising catalysts capable of converting the latter to formate and methanol while regenerating the scrubber. General trends regarding the influence of catalyst structure and reaction parameters on the efficiency, productivity, and selectivity of such processes will be highlighted. We will detail how this knowledge has informed the design of novel processes in which CO<small><sub>2</sub></small> is chemisorbed by amino acid-based solvents and hydrogenated <em>in situ</em> to formate and methanol, or alternatively used as a fuel to implement a “hydrogen battery” where, after metal-catalyzed H<small><sub>2</sub></small> release from formate, CO<small><sub>2</sub></small> is retained by the amino acid-based solvent in the “spent battery” which can then be recharged by hydrogenation of the retained CO<small><sub>2</sub></small> promoted by the same catalyst. The topic is still in its infancy, and several issues have emerged that will be critically discussed in the final section of this review. These issues need to be addressed in order to improve performance and provide a playground for researchers whose interest we hope to have aroused with this review.","PeriodicalId":68,"journal":{"name":"Chemical Society Reviews","volume":"111 1","pages":""},"PeriodicalIF":40.4000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Society Reviews","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cs00186b","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

In this review, we provide an overview of research efforts to integrate carbon dioxide capture specifically using amino acid-based sorbents with its thermocatalytic hydrogenation promoted by homogeneous metal complexes. Carbon capture and utilization (CCU) is a promising strategy for the production of fuels, chemicals and materials using CO2 scrubbed from point sources and the atmosphere as a C1 feedstock while mitigating CO2 emissions. Compared to established (alkanol)amines, amino acids offer some advantages as CO2 capture agents due to their lower volatility, higher oxygen stability and lower regeneration energies. We report how the structural diversity of amino acids and the possibility of combining them with cations in salts and ionic liquids have been exploited in the design of absorbers for improved absorption kinetics and capacity. Furthermore, we discuss selected examples from the literature illustrating the use of 1°/2° (poly)amines, since the 1°/2° amino groups are mainly responsible for CO2 chemisorption in amino acid-based capture media, the nature of the corresponding adducts, and the most promising catalysts capable of converting the latter to formate and methanol while regenerating the scrubber. General trends regarding the influence of catalyst structure and reaction parameters on the efficiency, productivity, and selectivity of such processes will be highlighted. We will detail how this knowledge has informed the design of novel processes in which CO2 is chemisorbed by amino acid-based solvents and hydrogenated in situ to formate and methanol, or alternatively used as a fuel to implement a “hydrogen battery” where, after metal-catalyzed H2 release from formate, CO2 is retained by the amino acid-based solvent in the “spent battery” which can then be recharged by hydrogenation of the retained CO2 promoted by the same catalyst. The topic is still in its infancy, and several issues have emerged that will be critically discussed in the final section of this review. These issues need to be addressed in order to improve performance and provide a playground for researchers whose interest we hope to have aroused with this review.

Abstract Image

均相催化加氢CO2 -氨基酸基捕获与利用
在这篇综述中,我们提供了研究工作的概述,特别是利用氨基酸基吸附剂的二氧化碳捕获与均相金属配合物促进的热催化加氢。碳捕获和利用(CCU)是一种很有前途的策略,用于生产燃料,化学品和材料,使用从点源和大气中洗涤的二氧化碳作为C1原料,同时减少二氧化碳排放。与已建立的(烷醇)胺相比,氨基酸由于其较低的挥发性、较高的氧稳定性和较低的再生能量,作为CO2捕集剂具有一些优势。我们报告了氨基酸的结构多样性以及它们与盐和离子液体中的阳离子结合的可能性如何在吸收剂的设计中得到利用,以改善吸收动力学和容量。此外,我们还讨论了从文献中选择的例子,说明了1°/2°(聚)胺的使用,因为1°/2°氨基主要负责氨基酸基捕获介质中CO2的化学吸附,相应的加合物的性质,以及最有前途的催化剂,能够将后者转化为甲酸盐和甲醇,同时再生洗涤器。将重点介绍催化剂结构和反应参数对这些过程的效率、生产率和选择性的影响的一般趋势。我们将详细介绍这些知识是如何为新工艺的设计提供信息的,在新工艺中,二氧化碳被氨基酸基溶剂化学吸附,并原位氢化成甲酸盐和甲醇,或者作为燃料来实现“氢电池”,在金属催化甲酸盐释放H2后,二氧化碳被氨基酸基溶剂保留在“废电池”中,然后可以通过相同催化剂促进保留的二氧化碳加氢来充电。该主题仍处于起步阶段,并且出现了几个问题,将在本综述的最后部分进行批判性讨论。这些问题需要得到解决,以提高性能,并为研究人员提供一个游乐场,我们希望通过这篇综述引起他们的兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemical Society Reviews
Chemical Society Reviews 化学-化学综合
CiteScore
80.80
自引率
1.10%
发文量
345
审稿时长
6.0 months
期刊介绍: Chemical Society Reviews is published by: Royal Society of Chemistry. Focus: Review articles on topics of current interest in chemistry; Predecessors: Quarterly Reviews, Chemical Society (1947–1971); Current title: Since 1971; Impact factor: 60.615 (2021); Themed issues: Occasional themed issues on new and emerging areas of research in the chemical sciences
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信