4.7 Article

Production of bio-ethanol by consecutive hydrogenolysis of corn-stalk cellulose

期刊

CHINESE JOURNAL OF CATALYSIS
卷 42, 期 5, 页码 844-854

出版社

SCIENCE PRESS
DOI: 10.1016/S1872-2067(20)63709-3

关键词

Corn-stalk; Cellulose Aqueous-phase hydrogenolysis; Bio-ethanol; Ni-WOx catalyst; Cu-0-Cu+ species; C-C bond cleavage

资金

  1. National Key Research and Development Program of China [2016YFB0701100]
  2. National Natural Science Foundation of China [21573075]

向作者/读者索取更多资源

This study developed a consecutive aqueous hydrogenolysis process to convert corn-stalk cellulose into a relatively high concentration of bio-ethanol, demonstrating good efficiency and economic viability. The multi-functional catalytic process provides an economically competitive route for the production of cellulosic ethanol from raw lignocellulose.
Current bio-ethanol production entails the enzymatic depolymerization of cellulose, but this process shows low efficiency and poor economy. In this work, we developed a consecutive aqueous hydrogenolysis process for the conversion of corn-stalk cellulose to produce a relatively high concentration of bio-ethanol (6.1 wt%) without humin formation. A high yield of cellulose (ca. 50 wt%) is extracted from corn stalk using a green solvent (80 wt% 1,4-butanediol) without destroying the structure of the lignin. The first hydrothermal hydrogenolysis step uses a Ni-WOx/SiO2 catalyst to convert the high cumulative concentration of cellulose (30 wt%) into a polyol mixture with a 56.5 C% yield of ethylene glycol (EG). The original polyol mixture is then subjected to subsequent selective aqueous-phase hydrogenolysis of the C-O bond to produce bioethanol (75% conversion, 84 C% selectivity) over the modified hydrothermally stable Cu catalysts. The added Ni component favors the good dispersion of Cu nanoparticles, and the incorporated Au3+ helps to stabilize the active Cu-0-Cu+ species. This multi-functional catalytic process provides an economically competitive route for the production of cellulosic ethanol from raw lignocellulose. (C) 2021, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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