Construction of Synergistic Co/CoO Interface to Enhance Hydrogenation Activity of Ethyl Lactate to 1,2‐Propanediol

Author:

Li Chengyang12,Wang Jia1ORCID,Zhao Jing3,Gao Guang1,Wu Kuang‐Hsu4,Su Bing‐Jian5,Chen Jin‐Ming5,Xi Yongjie1,Huang Zhiwei1,Qiao Yan6,Li Fuwei176ORCID

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences Lanzhou 730000 P. R. China

2. University of Chinese Academy of Sciences Beijing 100049 P. R. China

3. College of Petrochemical Technology Lanzhou University of Technology 730050 Lanzhou P. R. China

4. School of Chemical Engineering The University of New South Wales Sydney Kensington NSW 2052 Australia

5. National Synchrotron Radiation Research Center Hsinchu 30076 Taiwan

6. State Key Laboratory of Coal Conversion Institute of Coal Chemistry, Chinese Academy of Sciences Taiyuan 030001 P. R. China

7. School of Chemical Engineering University of Chinese Academy of Sciences Beijing 100049 P. R. China

Abstract

AbstractThe development of effective and stable non‐precious catalysts for hydrogenation of ester to diols remains a challenge. Herein, the catalytic hydrogenation of ethyl lactate (EL) to 1,2‐propanediol (1,2‐PDO) with supported Co catalysts derived from layered double hydroxides (LDHs) is investigated. Catalytic tests reveal that LDH‐derived Co catalysts exhibit the best catalytic performance with 98 % of EL conversion and >99 % of 1,2‐PDO selectivity at mild conditions, compared with other Co catalysts (supported on Al2O3, and TiO2) and LDH‐derived Cu catalysts. Due to the strong interaction among Co and Al matrix, the main composition is metallic Co0 and CoO after reduction at 600 °C. Besides, the catalyst shows good recyclability in the liquid phase hydrogenation. The superior catalytic performance can be attributed to the synergistic effect between Co0 and CoO, in which H2 molecule is activated on Co0 and EL is strongly adsorbed on CoO via hydroxyl groups.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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