Role of ReOx in Re-modified Rh/ZrO2 and Ir/ZrO2 catalysts in glycerol hydrogenolysis: Insights from first-principles study | |
Guan, Jing1; Chen, Xiufang1; Peng, Gongming1; Wang, Xicheng1; Cao, Quan1; Lan, Zhenggang1,2; Mu, Xindong1 | |
2013-09-01 | |
发表期刊 | CHINESE JOURNAL OF CATALYSIS |
卷号 | 34期号:9页码:1656-1666 |
摘要 | The thermodynamics of glycerol hydrogenolysis to produce 1,2‐propanediol (1,2‐PDO) and 1,3‐propanediol (1,3‐PDO) over Ru/ZrO2, Rh/ZrO2, ReOx‐Rh/ZrO2, and ReOx‐Ir/ZrO2 were studied using density functional theory calculations, with a special focus on the mechanism controlling the activity and selectivity of the reactions. It is found that the decomposition of glycerol on Ru/ZrO2 and Rh/ZrO2 proceeds through a dehydration‐hydrogenation mechanism. The formation of 1,2‐PDO is thermodynamically favored, and the activity of the Ru‐based catalyst is higher than that of the Rh‐based one. In contrast, a direct hydrogenolysis mechanism is proposed for the Re‐modified Rh and Ir catalysts, in which a dissociated H atom on the Rh(Ir) metal surface attacks the C–O bond neighboring the alkoxide species on the ReOx cluster. In the presence of ReOx‐Rh/ZrO2, the modified catalyst favors the production of 1,2‐PDO, and 1,3‐PDO production becomes competitive. However, the ReOx‐Ir/ZrO2 catalyst significantly improves 1,3‐PDO selectivity. The direct hydrogenolysis pathway, as opposed to the indirect hydrogenolysis mechanism for monometallic catalysts, may be the key to the high 1,3‐PDO selectivity on the modified catalysts, where the hydroxylated Re group facilitates the formation of terminal alkoxide species rather than secondary alkoxides. Steric effects are important in preferential terminal alkoxide formation on the ReOx‐Ir/ZrO2 catalysts because of the growth of large Ir‐Re clusters, resulting in high selectivity for 1,3‐PDO. ; The thermodynamics of glycerol hydrogenolysis to produce 1,2-propanediol (1,2-PDO) and 1,3-propanediol (1,3-PDO) over Ru/ZrO2, Rh/ZrO2, ReOx-Rh/ZrO2, and ReOx-Ir/ZrO2 were studied using density functional theory calculations, with a special focus on the mechanism controlling the activity and selectivity of the reactions. It is found that the decomposition of glycerol on Ru/ZrO2 and Rh/ZrO2 proceeds through a dehydration-hydrogenation mechanism. The formation of 1,2-PDO is thermodynamically favored, and the activity of the Ru-based catalyst is higher than that of the Rh-based one. In contrast, a direct hydrogenolysis mechanism is proposed for the Re-modified Rh and Ir catalysts, in which a dissociated H atom on the Rh(Ir) metal surface attacks the C-O bond neighboring the alkoxide species on the ReOx cluster. In the presence of ReOx-Rh/ZrO2, the modified catalyst favors the production of 1,2-PDO, and 1,3-PDO production becomes competitive. However, the ReOx-Ir/ZrO2 catalyst significantly improves 1,3-PDO selectivity. The direct hydrogenolysis pathway, as opposed to the indirect hydrogenolysis mechanism for monometallic catalysts, may be the key to the high 1,3-PDO selectivity on the modified catalysts, where the hydroxylated Re group facilitates the formation of terminal alkoxide species rather than secondary alkoxides. Steric effects are important in preferential terminal alkoxide formation on the ReOx-Ir/ZrO2 catalysts because of the growth of large Ir-Re clusters, resulting in high selectivity for 1,3-PDO. 2013, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved. |
文章类型 | Article |
关键词 | Density Functional Theory Glycerol Hydrogenolysis Propanediol Re-modified Metal Catalyst Thermodynamics |
学科领域 | 绿色化学催化 |
WOS标题词 | Science & Technology ; Physical Sciences ; Technology |
DOI | 10.1016/S1872-2067(12)60626-3 |
关键词[WOS] | AUGMENTED-WAVE METHOD ; ION-EXCHANGE-RESIN ; SELECTIVE HYDROGENOLYSIS ; MECHANISM ; SURFACE ; RUTHENIUM ; 1,3-PROPANEDIOL ; TEMPERATURE ; TRANSITION ; EFFICIENT |
收录类别 | SCI |
语种 | 英语 |
WOS研究方向 | Chemistry ; Engineering |
WOS类目 | Chemistry, Applied ; Chemistry, Physical ; Engineering, Chemical |
WOS记录号 | WOS:000324664900004 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.qibebt.ac.cn/handle/337004/1668 |
专题 | 绿色化学催化研究组 |
作者单位 | 1.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biobased Mat, Qingdao 266101, Shandong, Peoples R China 2.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao Key Lab Solar Energy Utilizat & Energy St, Qingdao 266101, Shandong, Peoples R China |
推荐引用方式 GB/T 7714 | Guan, Jing,Chen, Xiufang,Peng, Gongming,et al. Role of ReOx in Re-modified Rh/ZrO2 and Ir/ZrO2 catalysts in glycerol hydrogenolysis: Insights from first-principles study[J]. CHINESE JOURNAL OF CATALYSIS,2013,34(9):1656-1666. |
APA | Guan, Jing.,Chen, Xiufang.,Peng, Gongming.,Wang, Xicheng.,Cao, Quan.,...&Mu, Xindong.(2013).Role of ReOx in Re-modified Rh/ZrO2 and Ir/ZrO2 catalysts in glycerol hydrogenolysis: Insights from first-principles study.CHINESE JOURNAL OF CATALYSIS,34(9),1656-1666. |
MLA | Guan, Jing,et al."Role of ReOx in Re-modified Rh/ZrO2 and Ir/ZrO2 catalysts in glycerol hydrogenolysis: Insights from first-principles study".CHINESE JOURNAL OF CATALYSIS 34.9(2013):1656-1666. |
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