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Ni@C catalyzed hydrogenation of acetophenone to phenylethanol under industrial mild conditions in a flow reactor
Lin, Shanshan1,2; Liu, Jianguo3; Ma, Longlong3
2022-01-20
发表期刊REACTION CHEMISTRY & ENGINEERING
ISSN2058-9883
页码10
通讯作者Liu, Jianguo(liujg@seu.edu.cn) ; Ma, Longlong(mall@seu.edu.cn)
摘要The catalytic hydrogenation of organic substrates containing plenty of unsaturated functional groups is an important step in the industrial preparation of fine chemicals and has always been a hot spot in basic catalysis research. For example, phenylethanol obtained by the preferential hydrogenation of the C=O group of acetophenone is a valuable intermediate for the production of spices, flavors, and medicines. Furthermore, as the demand for 1-phenylethanol (PhE) continues to increase, the catalytic hydrogenation of acetophenone (AP) is becoming more and more important. At present, relatively few catalytic systems are used in this reaction as the hydrogenation of acetophenone is a complex multi-step reaction. Enantioselective hydrogenation on heterogeneous catalysts is remarkable due to its inherent operational and economic advantages, such as atom economy. It is one of the most ideal methods as the catalyst is easily separated and recycled. However, the traditional synthesis way in batch reactors usually takes a long time with unsatisfactory conversion which is not conducive to industrialization. Heterogeneous non-precious metal catalysts are advantageous for their implementation in flow reactor systems for industrial applications due to their ease of separation, low cost, and environmental friendliness. Herein, we report the first use of non-noble metal Ni-supported graphene-based catalysts for hydrogenation of acetophenone to phenylethanol with high efficiency in a flow reactor made of 316L stainless steel with a length of 200 mm and an inner diameter of 6 mm which can significantly improve mass and heat transfer. The conversion rate under the optimized reaction conditions can reach 99.14% with a satisfactory selectivity of 97.77% (the conversion and selectivity are in mol%). The magnetic catalyst has a compact structure, and the Ni particles coated with carbon on the surface are uniformly distributed. After 48 hours of uninterrupted continuous experiments, the conversion rate of acetophenone still reached 88.44%. The catalyst has good cyclability, and the Ni-based catalyst after the cycle still maintains high catalytic activity without obvious deactivation, and the catalyst structure remains intact and stable.
DOI10.1039/d1re00513h
关键词[WOS]LIQUID-PHASE HYDROGENATION ; TRANSFER REDUCTION ; SUPPORT ACIDITY ; NANOPARTICLES ; CHEMISTRY ; TOOLS ; METAL ; SIZE ; CO2
收录类别SCI
语种英语
资助项目National Key R&D Program of China[2018YFB1501500] ; National Natural Science Foundation of China[51976225]
WOS研究方向Chemistry ; Engineering
项目资助者National Key R&D Program of China ; National Natural Science Foundation of China
WOS类目Chemistry, Multidisciplinary ; Engineering, Chemical
WOS记录号WOS:000750978100001
出版者ROYAL SOC CHEMISTRY
引用统计
被引频次:2[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.giec.ac.cn/handle/344007/35786
专题中国科学院广州能源研究所
通讯作者Liu, Jianguo; Ma, Longlong
作者单位1.Chinese Acad Sci, Guangzhou Inst Energy Convers, CAS Key Lab Renewable Energy, Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Southeast Univ, Sch Energy & Environm, Key Lab Energy Thermal Convers & Control, Minist Educ, Nanjing 210096, Peoples R China
第一作者单位中国科学院广州能源研究所
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GB/T 7714
Lin, Shanshan,Liu, Jianguo,Ma, Longlong. Ni@C catalyzed hydrogenation of acetophenone to phenylethanol under industrial mild conditions in a flow reactor[J]. REACTION CHEMISTRY & ENGINEERING,2022:10.
APA Lin, Shanshan,Liu, Jianguo,&Ma, Longlong.(2022).Ni@C catalyzed hydrogenation of acetophenone to phenylethanol under industrial mild conditions in a flow reactor.REACTION CHEMISTRY & ENGINEERING,10.
MLA Lin, Shanshan,et al."Ni@C catalyzed hydrogenation of acetophenone to phenylethanol under industrial mild conditions in a flow reactor".REACTION CHEMISTRY & ENGINEERING (2022):10.
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