Low temperature one-pot synthesis of 1,1-diethoxyethane from ethanol on Bi/BiCeOx with strong metal-support interactions

被引:6
作者
An, Zhe [1 ]
Liu, Jiayu [1 ]
Cao, Meng [1 ]
Zhang, Jian [1 ]
Zhu, Yanru [1 ]
Song, Hongyan [1 ]
Xiang, Xu [1 ]
He, Jing [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
ethanol conversion; 1,1-diethoxyethane; strong metal-support interaction; Bi delta+-O-v-Ce-III sites; IN-SITU DRIFTS; SELECTIVE OXIDATION; DIRECT CONVERSION; CATALYSTS; TIO2; CEO2; ACETALDEHYDE; METHANOL; SURFACE; CERIA;
D O I
10.1007/s12274-022-4848-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The direct conversion of ethanol to 1,1-diethoxyethane (DEE) through one-pot dehydrogenation-acetalization has attracted broad interest from both academia and industry. Based on thermodynamics, the oxidative dehydrogenation of alcohol to acetaldehyde requires high temperature to activate oxygen to realize the C-H cleavage, while the acetalization of acetaldehyde with ethanol is exothermic reversible reaction favorable at low temperature. The mismatching of the reaction condition for the two consecutive steps makes it a great challenge to achieve both high ethanol conversion and high DEE selectivity. This work reports a highly efficient bi-functional catalysis by Bi/BiCeOx for one-pot oxidative dehydrogenation-acetalization route from ethanol to DEE under 150 degrees C and ambient pressure, affording a selectivity of 98.5% +/- 0.5% to DEE at an ethanol conversion of 87.0% +/- 1.0%. An efficient tandem catalysis has been achieved on the interfacial Bi delta+-O-v-Ce-III sites in Bi/BiCeOx established by strong metal-support interaction, in which Bi delta+-O-v- sites contribute to the oxidative dehydrogenation of ethanol at mild temperature, and -O-v-Ce-III sites to the subsequent acetalization between the generated acetaldehyde and ethanol.
引用
收藏
页码:3709 / 3718
页数:10
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