期刊文献+

Preparation and characterization of H_4SiW_(12)O_(40)@MIL-100(Fe) and its catalytic performance for synthesis of 4,4'-MDA 被引量:3

Preparation and characterization of H_4SiW_(12)O_(40)@MIL-100(Fe) and its catalytic performance for synthesis of 4,4'-MDA
下载PDF
导出
摘要 The catalytic performance of co mmonly used heteropolyacids (H3PW12O40, H4SiW12O40 and H3PMO12O40 synthesis of 4,4'-methylenedianiline (4,4'-MDA) from aniline and formaldehyde was evaluated and the result showed that H4SiW12O40 with moderate acid strength exhibited the best catalytic performance. Then HaSiW12O40@MIL-100(Fe) was prepared by encapsulating H4SiW12O40 within the pores of MIL-100(Fe) to facilitate its recovery and reuse. The prepared H4SiW12O40@MIL-100(Fe) was characterized by means of FT-IR, N2 adsorption-desorption, XRD, TG and then the catalytic performance was evaluated. The result showed that H4SiW12O40 was highly dispersed in the pores of MIL-100(Fe), and both the Keggin structure of HaSiW12O40 and the crystal skeleton structure of MIL-100(Fe) could be effectively/preserved. Furthermore, H4SiW12O40@ MIL-100(Fe) showed excellent catalytic performance under the following reaction conditions: a molar ratio of aniline to formaldehyde = 5, a mass ratio of catalyst to formaldehyde = 1.2, a reaction temperature of 120 ℃ and a reaction time of 6 h. Under the above reaction conditions, the conversion of aniline was 41.1%, and the yield and selectivity of 4,4'-MDA were 81,6% and 79.2%, respectively. Unfortunately, an appreciable loss in the catalytic activity of the recovered H4SiW12O40@MIL-100(Fe) was observed because of the blocking of the pores and the change of the acidity resulted from the adsorption of alkaline organics such as aniline and 4,4'-MDA. The adsorbed alkaline organics could be cleaned up when the recovered catalyst was washed by methanol and DMF. Then the catalyst was effectively reused up to three cycles without much loss in its activity. The catalytic performance of commonly used heteropoly acids(H_3 PW_(12)O_(40). H_4 SiW_(12)O_(40) and H_3 PMo_(12)O_(40)) for the synthesis of 4,4'-methylenedianiline(4.4'-MDA) from aniline and formaldehyde was evaluated and the result showed that H_4 SiW_(12)O_(40) with moderate acid strength exhibited the best catalytic performance. Then H_4 SiW_(12)O_(40)@MIL-100(Fe) was prepared by encapsulating H_4 SiW_(12)O_(40) within the pores of MIL-100(Fe) to facilitate its recovery and reuse. The prepared H_4 SiW_(12)O_(40)@MIL-100(Fe) was characterized by means of FT-IR, N_2 adsorption-desorption, XRD, TG and then the catalytic performance was evaluated. The result showed that H_4 SiW_(12)O_(40) was highly dispersed in the pores of MIL-100(Fe), and both the Keggin structure of H_4 SiW_(12)O_(40)and the crystal skeleton structure of MIL-100(Fe) could be effectively preserved. Furthermore. H_4 SiW_(12)O_(40)@MIL-100(Fe) showed excellent catalytic performance under the following reaction conditions: a molar ratio of aniline to formaldehyde = 5, a mass ratio of catalyst to formaldehyde = 1.2, a reaction temperature of 120 ℃and a reaction time of 6 h. Under the above reaction conditions, the conversion of aniline was 41.1%, and the yield and selectivity of 4.4'-MDA were 81.6% and 79.2%, respectively. Unfortunately, an appreciable loss in the catalytic activity of the recovered H_4 SiW_(12)O_(40)@MIL-100(Fe) was observed because of the blocking of the pores and the change of the acidity resulted from the adsorption of alkaline organics such as aniline and 4,4'-MDA.The adsorbed alkaline organics could be cleaned up when the recovered catalyst was washed by methanol and DMF. Then the catalyst was effectively reused up to three cycles without much loss in its activity.
出处 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2018年第2期330-336,共7页 中国化学工程学报(英文版)
基金 Supported by the National Natural Science Foundation of China(21236001,21476058,21506046)
关键词 H4SiW12 O40@MIL- 100 Fe )Catalyst activation 4 4'-Methylenedianilinc synthesis Mukiphase reaction Stability 催化性能 H4SiW12O40 表演 合成 解吸附作用 Keggin 骨骼结构 反应条件
  • 相关文献

参考文献5

二级参考文献65

共引文献34

同被引文献10

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部