Porous metal-organic framework with Lewis acid - base bifunctional sites for high efficient CO2 adsorption and catalytic conversion to cyclic carbonates

被引:39
作者
Li, Jing [1 ]
Li, Wen-Jun [2 ]
Xu, Shi-Cheng [3 ]
Li, Bo [3 ]
Tang, Ying [4 ,5 ]
Lin, Zhen-Fang [6 ]
机构
[1] Xian Univ, Sch Chem Engn, Xian 710065, Shaanxi, Peoples R China
[2] Seventh Peoples Hosp Chengdu, Prenatal Diag Ctr, Chengdu, Sichuan, Peoples R China
[3] Bazhong Cent Hosp, Dept Neurol, Bazhong, Sichuan, Peoples R China
[4] Xian Shiyou Univ, Shaanxi Prov Key Lab Environm Pollut Control & Re, Xian 710065, Shaanxi, Peoples R China
[5] CNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
[6] Chengdu Univ TCM, Affiliated Sichuan Prov Rehabil Hosp, Dept Neurol, Sichuan Bayi Rehabil Ctr, Chengdu, Sichuan, Peoples R China
关键词
Metal-organic framework; Bifunctional sites; CO2; sorption; conversion; CYCLOADDITION; CAPTURE; FIXATION; DIOXIDE;
D O I
10.1016/j.inoche.2019.05.031
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A highly porous three-dimensional (3D) metal-organic framework (MOF) [Ni-3(BTC)(2)(MA)(H2O)](DMF)(7) (1) incorporating both exposed metal sites and nitrogen-rich melamine was successfully constructed via solvothermal assembly of 1,3,5-benzenetricarboxylic acid (H3BTC), melamine (MA) and Ni(II) ions. The resulting activated Ni(II)-MOF-1a features high CO2 loading capacity and excellent CO2 affinity due to the Lewis-base property together with abundant micropores. The heterogeneous catalytic activity of the activated Ni(II)-MOF-1a was confirmed by remarkably high efficiency on CO2 cycloaddition with small epoxides under ambient conditions. Moreover, the Ni(II)-MOF-1a exhibited satisfied stability and versatility, and it was easy to recycle with no obvious decrease of catalytic activity. Then the feasible synergistic mechanism of Ni(II)-MOF/Bu4NBr catalysts for CO2 conversion was proposed.
引用
收藏
页码:70 / 75
页数:6
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