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Intensified gas-phase hydrogenation of acetone to isopropanol catalyzed at metal-oxide interfacial sites
2023-02-15
发表期刊CHEMICAL ENGINEERING JOURNAL (IF:13.3[JCR-2023],13.2[5-Year])
ISSN1385-8947
EISSN1873-3212
卷号454
发表状态已发表
DOI10.1016/j.cej.2022.140059
摘要The gas-phase acetone hydrogenation to isopropanol is an environmentally benign process relevant to chemical, energy and medical fields, but the catalysts qualified at low temperature and pressure remain challenging. Herein, we show the intensified gas-phase hydrogenation of acetone to isopropanol at metal-oxide interface. The Pt/CeO catalyst with highly active and stable Pt-CeO interface delivers 92 % acetone conversion with 99 % isopropanol selectivity at 80 °C, weight hourly space velocity of 10 h, H/acetone molar ratio of 2, and 0.1 MPa, and its catalytic performance is preserved during a single-running test of 200 h. A series of electron microscopic, thermal, and spectroscopic analyses testify that acetone could be efficiently adsorbed on oxygen vacancy at Pt-CeO interface. The H atoms dissociated by Pt spill over to the interface to hydrogenate the chemically-adsorbed acetone thereon to form isopropanol. Inspired by such observation, the Pt-CeO interface was extended to other metal-oxide interfaces (metal: Pt and Ni; oxide: CeO, TiO, ZrO and FeO), all exhibiting excellent catalytic performance. For example, the Ni/CeO could offer 91 % acetone conversion and 99 % isopropanol selectivity, identical to that of Pt/CeO under the same conditions. This work particularly investigated the acetone adsorption at the metal-oxide interface, establishing the foundation for rational design of high cost performance catalysts for aldehydes/ketones hydrogenation and other reactions.
关键词Acetone adsorption Acetone hydrogenation Interface catalysis Isopropanol Metal-oxide interface Oxygen vacancy
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收录类别EI ; SCI ; SCOPUS
语种英语
资助项目National Natural Science Foundation of China["22179038","21703069"] ; Special Project for Peak Carbon Dioxide Emissions-Carbon Neutrality from the Shanghai Municipal Science and Technology Commission[21DZ1206700] ; Academic Promotion Programme of Shandong First Medical University[2019QL008]
WOS研究方向Engineering
WOS类目Engineering, Environmental ; Engineering, Chemical
WOS记录号WOS:000916038800005
出版者ELSEVIER SCIENCE SA
EI入藏号20224413051556
EI主题词Hydrogenation
EI分类号641.1 Thermodynamics ; 801.4 Physical Chemistry ; 802.2 Chemical Reactions ; 802.3 Chemical Operations ; 803 Chemical Agents and Basic Industrial Chemicals ; 804 Chemical Products Generally ; 804.1 Organic Compounds ; 804.2 Inorganic Compounds ; 933.1 Crystalline Solids
原始文献类型Journal article (JA)
Scopus 记录号2-s2.0-85141002629
来源库Scopus
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文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/243473
专题物质科学与技术学院_博士生
物质科学与技术学院_PI研究组_杨永组
通讯作者Zhao, Guofeng
作者单位
1.Shandong First Med Univ & Shandong Acad Med Sci, Inst Opt Funct Mat Biomed Imaging, Sch Chem & Pharmaceut Engn, Tai An 271016, Peoples R China
2.East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
3.ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
4.Zhejiang Univ, Dept Chem, Hangzhou 310058, Peoples R China
5.Zhejiang Xinhua Chem CO LTD, Jiande 311607, Peoples R China
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GB/T 7714
Liu, Kun,Sun, Yongbin,Feng, Jie,et al. Intensified gas-phase hydrogenation of acetone to isopropanol catalyzed at metal-oxide interfacial sites[J]. CHEMICAL ENGINEERING JOURNAL,2023,454.
APA Liu, Kun.,Sun, Yongbin.,Feng, Jie.,Liu, Yang.,Zhu, Jian.,...&Zhao, Guofeng.(2023).Intensified gas-phase hydrogenation of acetone to isopropanol catalyzed at metal-oxide interfacial sites.CHEMICAL ENGINEERING JOURNAL,454.
MLA Liu, Kun,et al."Intensified gas-phase hydrogenation of acetone to isopropanol catalyzed at metal-oxide interfacial sites".CHEMICAL ENGINEERING JOURNAL 454(2023).
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