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首页> 外文期刊>Chemical Engineering Research & Design: Transactions of the Institution of Chemical Engineers >Zn-2(C9H3O6)(C4H5N2)(C4H6N2)(3) MOF as a highly efficient catalyst for chemical fixation of CO2 into cyclic carbonates and kinetic studies
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Zn-2(C9H3O6)(C4H5N2)(C4H6N2)(3) MOF as a highly efficient catalyst for chemical fixation of CO2 into cyclic carbonates and kinetic studies

机译:Zn-2(C9H3O6)(C4H5N2)(C4H5N2)(3)MOF作为CO 2的化学固定成循环碳酸盐和动力学研究的高效催化剂

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摘要

Zn-2(C9H3O6)(C4H5N2)(C4H6N2)(3) (Zn-BTC-2MeIm) was hydrothermally synthesized and employed as a highly efficient catalyst for CO2 coupling with epichlorohydrin (ECH). Various techniques such as XRD, FT-IR, XPS, TG-DTG, NH3/CO2-TPD were employed for characterizing the compound. Interestingly, TG profile illustrated the Zn-BTC-2MeIm was stable above 200 degrees C. The highest catalytic activity of 98.93% conversion of ECH and 98.32% selectivity to chloropropene carbonate was observed under the optimum conditions (100 degrees C, 120 mesh, 1000 rpm, 3.0 MPa, 6 h, 0.75 wt.% of ECH). Besides, the recyclability results exhibited ZnBTC-2MeIm compound could be reused no less than three times with a slight reduction in its catalytic ability. Moreover, coupling results of CO2 with other epoxides showed this compound could efficiently convert various epoxides into cyclic carbonates. Finally, the investigation of the kinetic exhibited the law of CO2 coupling with ECH was coincident with the first order kinetic and the activation energy (E-a) was to be 113.38 kJ/mol. (C) 2018 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:Zn-2(C 2 H 3 O 6)(C4H5N2)(C4H5N2)(3)(Zn-BTC-2meIM)被水热合成,用作与表氯醇(ECH)的CO 2偶联的高效催化剂。采用各种技术,例如XRD,FT-IR,XPS,TG-DTG,NH 3 / CO2-TPD用于表征化合物。有趣的是,TG谱图所示的Zn-BTC-2meim稳定在200摄氏度上方稳定。在最佳条件下观察到98.93%的催化活性为98.93%转化率为98.32%的选择性(100℃,120目,1000 RPM,3.0 MPa,6小时,0.75重量%的ZH)。此外,可回收性结果表现出ZnBTC-2meim化合物可以重复使用不少于三次,其催化能力略微降低。此外,CO 2与其他环氧化物的偶联结果显示该化合物可以有效地将各种环氧化物转化为环状碳酸盐。最后,随着第一阶动力学和激活能量(E-A)为113.38kj / mol,对eq2偶联的CO 2偶联定律表现出对CO 2偶联的定律。 (c)2018化学工程师机构。 elsevier b.v出版。保留所有权利。

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