Rational Design of Cobalt Complexes Based on the trans Effect of Hybrid Ligands and Evaluation of their Catalytic Activity in the Cycloaddition of Carbon Dioxide with Epoxide

2020 ◽  
Vol 39 (19) ◽  
pp. 3546-3561 ◽  
Author(s):  
Wen-Yue Song ◽  
Qiuli Liu ◽  
Qingqing Bu ◽  
Donghui Wei ◽  
Bin Dai ◽  
...  
2015 ◽  
Vol 641 (12-13) ◽  
pp. 2147-2156 ◽  
Author(s):  
Artjom Döring ◽  
Ulrich Flörke ◽  
Alexander Hoffmann ◽  
Matthew D. Jones ◽  
Dirk Kuckling ◽  
...  

Author(s):  
Hans C. Hendrikse ◽  
Alejo Aguirre ◽  
Arno van der Weijden ◽  
Anne S. Meeussen ◽  
Fernanda Neira D’Angelo ◽  
...  

2019 ◽  
Vol 126 ◽  
pp. 229-237 ◽  
Author(s):  
Naeem Mahmood Ashraf ◽  
Akshaya Krishnagopal ◽  
Aadil Hussain ◽  
David Kastner ◽  
Ahmed Mahmoud Mohammed Sayed ◽  
...  

2016 ◽  
Vol 16 (2) ◽  
pp. 2024-2027
Author(s):  
Ho-Geun Ahn ◽  
Hwan-Gyu Lee ◽  
Min-Chul Chung ◽  
Kwon-Pil Park ◽  
Ki-Joong Kim ◽  
...  

Author(s):  
Oscar Felipe Arbeláez-Pérez ◽  
Sara Dominguez Cardozo ◽  
Andrés Felipe Orrego-Romero ◽  
Aida Luz Villa Holguin ◽  
Felipe Bustamante Londoño

The catalytic activity for dimethyl carbonate formation from carbon dioxide and methanol over mono and bimetallic Cu:Ni supported on activated carbon is presented. Bimetallic catalysts exhibit higher catalytic activity than the monometallic samples, being Cu:Ni-2:1 (molar ratio) the best catalyst; X-Ray diffraction, transmission electron microscopy, and metal dispersion analysis provided insight into the improved activity. In situ FT-IR experiments were conducted to investigate the mechanism of formation of dimethyl carbonate from methanol and carbon dioxide over Cu-Ni:2-1. The kinetics of the direct synthesis of dimethyl carbonate in gas phase over Cu:Ni-2:1 supported on activated carbon catalyst was experimentally investigated at 12 bar and temperatures between 90 oC and 130 oC, varying the partial pressures of CO2 and methanol. Experimental kinetic data were consistent with a Langmuir–Hinshelwood model that included carbon dioxide and methanol adsorption on catalyst actives sites (Cu, Ni and Cu-Ni), and the reaction of adsorbed CO2 with methoxi species as the rate determining step. The estimated apparent activation energy was 94.2 kJ mol-1.


2012 ◽  
Vol 549 ◽  
pp. 445-448
Author(s):  
Li Dan Fan ◽  
Gang Qin ◽  
Xin Xin Cao ◽  
Shao Kui Cao

A novel catalyst for the copolymerization of CO2 and cyclohexene oxide(CHO) was prepared by using BTE and ZnCl2. The zinc complex showed catalytic activity for the copolymerization. The obtained copolymer was characterized by IR and NMR. Effect of reaction time on copolymerization was investigated.


Nanoscale ◽  
2018 ◽  
Vol 10 (25) ◽  
pp. 11869-11880 ◽  
Author(s):  
Arun Prakash Periasamy ◽  
Rini Ravindranath ◽  
Sakkarapalayam Murugesan Senthil Kumar ◽  
Wen-Ping Wu ◽  
Ting-Rui Jian ◽  
...  

Cu2O(OL-MH)/Ppy particles selectively reduce CO2to methanol with a faradaic efficiency of 93 ± 1.2% due to an efficient anion exchange mechanism, dominant low-index (111) facets and high-index (311), (211) facets of Cu2O.


2018 ◽  
Vol 1 (3) ◽  
pp. 1150-1163 ◽  
Author(s):  
Wei Cai ◽  
Qin Zhong ◽  
Dongyu Wang ◽  
Yunxia Zhao ◽  
Mindong Chen ◽  
...  

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