CO2催化制备高附加值多碳含氧化合物的研究进展OA北大核心CSTPCD
Research progress on CO2 catalytic conversion to value-added oxygenates
将温室气体CO2通过化学反应路径制备高附加值多碳含氧化合物如乙醇、乙酸、丙醛、丙酸、丁醇等具有挑战性.由于C-C偶联反应的复杂性和成键的不可控性,导致合成多碳高值含氧化合物困难.本工作总结了近期在连续流固定床条件下CO2催化合成高附加值多碳含氧化合物的研究进展.首先归纳了 CO2加氢路径下可能的反应机理;其次总结了 CO2直接加氢(一步法、串联法)、CO2与轻烃重整、CO2氢甲酰化等不同反应路径下具有潜力的催化剂,包括金属碳化物、碱金属修饰的Cu、Fe、Co、Rh等单金属或二元金属制备多碳高值含氧化合物的特点,并进一步阐述了不同催化剂上的作用机制.最后对目前存在的问题和未来可能的解决方案进行了讨论和展望.
Chemical conversion of greenhouse gas CO2 into value-added oxygenates such as ethanol,acetic acid,propanal,propionic acid,butanol,etc.is challenging due to the complexity of C-C coupling and the uncontrollable bonding.In this review,recent research progresses on the synthesis of multi-carbon oxygenates from CO2 in fixed bed reactor are provided.Firstly,the reaction mechanisms of CO2 hydrogenation are summarized.Then,the potential catalysts applied in one-step or tandem CO2 hydrogenation,dry reforming with light hydrocarbons and hydroformylation were introduced over metal carbides,alkali metal modified single or binary metal catalysts such as Cu,Fe,Co,Rh,etc.The reaction mechanism over different catalysts were further elaborated.Finally,the problems and outlook are discussed.
李永恒;吴冲冲;王文波;辛靖;米晓彤;杨国明;苏梦军;张斯然;李洪宝
中海油化工与新材料科学研究院,北京,102209
化学
二氧化碳转化多碳含氧化合物一步法串联催化
CO2 conversionmulti-carbon oxygenatesone-step methodtandem catalysis
《燃料化学学报（中英文）》 2024 (004)
496-511 / 16
The project was supported by CNOOC Science and Technology Projects(KJGG-2022-12-CCUS-030401,030402).中国海洋石油集团有限公司科技项目(KJGG-2022-12-CCUS-030401,030402)资助
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