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ShanghaiTech University Knowledge Management System
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]) |
ISSN | 1385-8947 |
EISSN | 1873-3212 |
卷号 | 454 |
发表状态 | 已发表 |
DOI | 10.1016/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 |
URL | 查看原文 |
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 |
引用统计 | 正在获取...
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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 |
推荐引用方式 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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