| Literature DB >> 29660228 |
Lingxiang Wang1, Liang Wang1, Jian Zhang1,2, Xiaolong Liu3, Hai Wang1, Wei Zhang4, Qi Yang5, Jingyuan Ma5, Xue Dong6, Seung Jo Yoo7, Jin-Gyu Kim7, Xiangju Meng1, Feng-Shou Xiao1,2.
Abstract
Methods for the hydrogenation of CO2 into valuable chemicals are in great demand but their development is still challenging. Herein, we report the selective hydrogenation of CO2 into ethanol over non-noble cobalt catalysts (CoAlOx ), presenting a significant advance for the conversion of CO2 into ethanol as the major product. By adjusting the composition of the catalysts through the use of different prereduction temperatures, the efficiency of CO2 to ethanol hydrogenation was optimized; the catalyst reduced at 600 ° gave an ethanol selectivity of 92.1 % at 140 °C with an ethanol time yield of 0.444 mmol g-1 h-1 . Operando FT-IR spectroscopy revealed that the high ethanol selectivity over the CoAlOx catalyst might be due to the formation of acetate from formate by insertion of *CHx , a key intermediate in the production of ethanol by CO2 hydrogenation.Entities:
Keywords: carbon dioxide; cobalt; ethanol; heterogeneous catalysis; hydrogenation
Year: 2018 PMID: 29660228 DOI: 10.1002/anie.201800729
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336