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Low-pressure CO2 fixation with epoxides via a new modified nano crystalline NH2-MIL-101(Cr) in Solvent-free and cocatalyst free condition
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Vocke, Heinrich
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Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran

Bottke, Patrick
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Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran

Zastrau, May-Franzis
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Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran

Weers, Marco
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Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran

Wark, Michael
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Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran
机构:
[1] Univ Mohaghegh Ardabili, Fac Basic Sci, Dept Chem, Ardebil 179, Iran
[2] Carl von Ossietzky Univ Oldenburg, Inst Chem, Chem Technol 1, Carl von Ossietzky Str 9-11, D-26129 Oldenburg, Germany
关键词:
CO2;
fixation;
MIL-101(Cr);
Epoxide;
Solvent free;
Cocatalyst free;
METAL-ORGANIC FRAMEWORKS;
CARBON-DIOXIDE;
CHEMICAL FIXATION;
ADSORPTION;
CYCLOADDITION;
MIL-101(CR);
MOF;
CATALYST;
OXIDE;
D O I:
10.1016/j.jcou.2022.102366
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Incorporation of appropriate Lewis acid centers such as Cr3+ and nucleophilic ionic species such as Br- as as-sistants in the opening of epoxy rings, on the metal-organic frameworks can be considered an efficient catalyst in a CO2 fixation processes. In this research work, we introduce a new catalyst by modifying the metal-organic framework and creating the ammonium salt with bromide, TEAB-MIL-101(Cr). The catalyst was characterized using several appropriate techniques and used as catalyst in the CO2 fixation reaction of a large number of epoxides. The catalytic reaction was pushed forward under solvent and cocatalyst-free conditions at 1.5 bar of CO2. The catalyst showed high activity in the presence of most epoxides, but the best result was related to epichlorohydrin, which showed 99 % conversion and 96 % selectivity to the respective cyclic carbonate within 3 h. The prepared catalyst was easily recovered and reused to the catalytic process for at least fifth times without any noticeable change in activity.
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