Selectivity control in CO 2 hydrogenation to one-carbon products

被引:19
|
作者
Hu, Jingting [1 ]
Cai, Yafeng [1 ]
Xie, Jinghao [1 ]
Hou, Deshan [1 ,2 ]
Yu, Liang [1 ,2 ]
Deng, Dehui [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Collaborat Innovat Ctr Chem Energy Mat, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
CHEM | 2024年 / 10卷 / 04期
基金
国家重点研发计划; 中国国家自然科学基金; 中国博士后科学基金;
关键词
METAL-SUPPORT INTERACTIONS; GAS SHIFT REACTION; METHANOL SYNTHESIS; ACTIVE-SITE; HETEROGENEOUS CATALYSIS; ALKALI ADDITIVES; OXIDE-SUPPORT; METHANATION; MECHANISM; REDUCTION;
D O I
10.1016/j.chempr.2024.02.017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO 2 hydrogenation to value-added chemicals offers a promising route for alleviating the energy crisis and climate warming. Highly selective CO 2 hydrogenation is of great significance for reducing the costs of separation and circulation and improving production efficiency. However, it remains a great challenge due to the complex reaction network and co -existence of multiple active sites on catalysts. This review concentrates on the selectivity control in CO 2 hydrogenation to one -carbon (C1) products, including methanol, CO, and CH 4 , which are the simplest CO 2 hydrogenation products and basic chemical building blocks. Based on the development of different catalyst systems, we here discuss multi -factors that affect CO 2 hydrogenation selectivity, including reaction conditions, such as temperature and pressure, and catalyst properties, such as active metal, metal dispersion, support, and promoter. We conclude the review by summarizing general rules for manipulating CO 2 hydrogenation selectivity toward C1 products, discussing remaining challenges, and highlighting future opportunities of CO 2 hydrogenation.
引用
收藏
页码:1084 / 1117
页数:34
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