Investigation of supported Zn(OAc)2 catalyst and its stability in N-phenyl carbamate synthesis

被引:31
|
作者
Li, Fang [1 ]
Li, Wenbo [1 ]
Li, Jing [2 ]
Xue, Wei [1 ]
Wang, Yanji [1 ]
Zhao, Xinqiang [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Hebei Prov Key Lab Green Chem Technol & High Effi, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Sch Civil Engn, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
N-Phenyl carbamate; Aniline; Dimethyl carbonate; Zn(OAc)(2)/SiO2; DIMETHYL CARBONATE; ZINC ACETATE; OXIDATIVE CARBONYLATION; METHOXYCARBONYLATION; ANILINE; DICARBAMATE; DIAMINES; AMINES;
D O I
10.1016/j.apcata.2014.01.008
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
Zn(OAc)(2) was found to give excellent catalytic performance for methyl N-phenyl carbamate (MPC) synthesis from aniline and dimethyl carbonate (DMC). However, after being used for only once it tended to lose activity because of the formation of ZnO by the reaction of Zn(OAc)(2) and methanol. Zn(OAc)(2)/SiO2 was prepared by incipient impregnation and it gave excellent catalytic performance in MPC synthesis, on which aniline conversion and MPC yield were 98.1% and 93.8%, respectively. And Zn(OAc)(2)/SiO2 was found to be more stable than Zn(OAc)(2) during the reaction. When Zn(OAc)(2)/SiO2 was used for the fifth time, aniline conversion and MPC yield were found to be 64.3% and 38.1%, respectively. The Zn(OAc)(2)/SiO2 catalyst was characterized by TG-DTA, ICP, FTIR, XRD and XPS. The characterization results suggested that the deactivation of Zn(OAc)(2)/SiO2 was also due to the formation of ZnO and there were two reasons for the improved stability of Zn(OAc)(2)/SiO2 catalyst. One was the formation of the Si-O-Zn bonds in Zn(OAc)(2)/SiO2 catalyst, which increased the steric hindrance of Zn and consequently retarded the reaction between Zn(OAc)(2) and methanol. The other cause was the dehydration between methanol and the hydroxyl group on the SiO2 surface, which reduced the chance of a reaction between methanol and Zn(OAc)(2). (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:355 / 362
页数:8
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