用Pt-Ni@C催化剂从纤维素水相中生产乙醇

Q3 Energy
Xiao LU , Zhouwen LI , Li ZHAO , Xuewei ZHANG , Guangmai ZHAO , Kaixin JIN , Wanpeng LI , Haiyong WANG , Dalei ZHANG , Chenguang WANG
{"title":"用Pt-Ni@C催化剂从纤维素水相中生产乙醇","authors":"Xiao LU ,&nbsp;Zhouwen LI ,&nbsp;Li ZHAO ,&nbsp;Xuewei ZHANG ,&nbsp;Guangmai ZHAO ,&nbsp;Kaixin JIN ,&nbsp;Wanpeng LI ,&nbsp;Haiyong WANG ,&nbsp;Dalei ZHANG ,&nbsp;Chenguang WANG","doi":"10.1016/S1872-5813(24)60524-4","DOIUrl":null,"url":null,"abstract":"<div><div>A series of Pt-Ni@C catalysts with different Pt/Ni@C mass ratios were prepared using deposition precipitation method. The effect of the loading amounts of Pt on the synthesis of ethanol by cellulose hydrogenation reduction was studied. The structure-performance relationship of the catalyst was clarified. The results showed that the Pt/Ni@C catalyst achieved the complete conversion of high concentration of cellulose under H<sub>2</sub> environment at 200 ℃, 5.5 MPa. When the concentration of cellulose reached 50 g/L, the ethanol concentration in the solution was 13.3 g/L with yield of 31%. The valence state of the Pt species, the ordering degree of carbon and the microstructure of the catalyst were characterized by means of XRD, XPS, Raman and TEM. The Ni atoms wrapped by the carbon layer of the catalyst showed an electron-rich state through electron migration with the surface carbon layer. The electron-negative surface of Pt-Ni@C effectively break the C–O and C–C bonds of the intermediates. Compared with traditional carbon-based catalysts, the amount of surface active sites increased by loading small amount of Pt. The Pt promoted the activation of hydrogen, and the synergistic of electron-rich surface and the trace phosphoric acid led to excellent activity of the Pt-Ni@C.</div></div>","PeriodicalId":15956,"journal":{"name":"燃料化学学报","volume":"53 6","pages":"Pages 863-871"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Production of ethanol from cellulose in aqueous phase with Pt-Ni@C catalysts\",\"authors\":\"Xiao LU ,&nbsp;Zhouwen LI ,&nbsp;Li ZHAO ,&nbsp;Xuewei ZHANG ,&nbsp;Guangmai ZHAO ,&nbsp;Kaixin JIN ,&nbsp;Wanpeng LI ,&nbsp;Haiyong WANG ,&nbsp;Dalei ZHANG ,&nbsp;Chenguang WANG\",\"doi\":\"10.1016/S1872-5813(24)60524-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A series of Pt-Ni@C catalysts with different Pt/Ni@C mass ratios were prepared using deposition precipitation method. The effect of the loading amounts of Pt on the synthesis of ethanol by cellulose hydrogenation reduction was studied. The structure-performance relationship of the catalyst was clarified. The results showed that the Pt/Ni@C catalyst achieved the complete conversion of high concentration of cellulose under H<sub>2</sub> environment at 200 ℃, 5.5 MPa. When the concentration of cellulose reached 50 g/L, the ethanol concentration in the solution was 13.3 g/L with yield of 31%. The valence state of the Pt species, the ordering degree of carbon and the microstructure of the catalyst were characterized by means of XRD, XPS, Raman and TEM. The Ni atoms wrapped by the carbon layer of the catalyst showed an electron-rich state through electron migration with the surface carbon layer. The electron-negative surface of Pt-Ni@C effectively break the C–O and C–C bonds of the intermediates. Compared with traditional carbon-based catalysts, the amount of surface active sites increased by loading small amount of Pt. The Pt promoted the activation of hydrogen, and the synergistic of electron-rich surface and the trace phosphoric acid led to excellent activity of the Pt-Ni@C.</div></div>\",\"PeriodicalId\":15956,\"journal\":{\"name\":\"燃料化学学报\",\"volume\":\"53 6\",\"pages\":\"Pages 863-871\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"燃料化学学报\",\"FirstCategoryId\":\"1087\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872581324605244\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Energy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"燃料化学学报","FirstCategoryId":"1087","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872581324605244","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0

摘要

采用沉积沉淀法制备了一系列Pt/Ni@C质量比不同的Pt-Ni@C催化剂。研究了铂的负载量对纤维素加氢还原合成乙醇的影响。澄清了催化剂的结构与性能关系。结果表明,Pt/Ni@C催化剂在H2环境下,在200℃、5.5 MPa条件下实现了高浓度纤维素的完全转化。当纤维素浓度达到50 g/L时,溶液中乙醇浓度为13.3 g/L,产率为31%。采用XRD、XPS、Raman和TEM等手段对催化剂的价态、碳有序度和微观结构进行了表征。被催化剂碳层包裹的Ni原子通过与表面碳层的电子迁移呈现富电子态。Pt-Ni@C的电子负表面有效地破坏了中间产物的C-O和C-C键。与传统碳基催化剂相比,少量Pt的负载增加了表面活性位点的数量。Pt促进了氢的活化,富电子表面与微量磷酸的协同作用使得Pt-Ni@C具有优异的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of ethanol from cellulose in aqueous phase with Pt-Ni@C catalysts
A series of Pt-Ni@C catalysts with different Pt/Ni@C mass ratios were prepared using deposition precipitation method. The effect of the loading amounts of Pt on the synthesis of ethanol by cellulose hydrogenation reduction was studied. The structure-performance relationship of the catalyst was clarified. The results showed that the Pt/Ni@C catalyst achieved the complete conversion of high concentration of cellulose under H2 environment at 200 ℃, 5.5 MPa. When the concentration of cellulose reached 50 g/L, the ethanol concentration in the solution was 13.3 g/L with yield of 31%. The valence state of the Pt species, the ordering degree of carbon and the microstructure of the catalyst were characterized by means of XRD, XPS, Raman and TEM. The Ni atoms wrapped by the carbon layer of the catalyst showed an electron-rich state through electron migration with the surface carbon layer. The electron-negative surface of Pt-Ni@C effectively break the C–O and C–C bonds of the intermediates. Compared with traditional carbon-based catalysts, the amount of surface active sites increased by loading small amount of Pt. The Pt promoted the activation of hydrogen, and the synergistic of electron-rich surface and the trace phosphoric acid led to excellent activity of the Pt-Ni@C.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
燃料化学学报
燃料化学学报 Chemical Engineering-Chemical Engineering (all)
CiteScore
2.80
自引率
0.00%
发文量
5825
期刊介绍: Journal of Fuel Chemistry and Technology (Ranliao Huaxue Xuebao) is a Chinese Academy of Sciences(CAS) journal started in 1956, sponsored by the Chinese Chemical Society and the Institute of Coal Chemistry, Chinese Academy of Sciences(CAS). The journal is published bimonthly by Science Press in China and widely distributed in about 20 countries. Journal of Fuel Chemistry and Technology publishes reports of both basic and applied research in the chemistry and chemical engineering of many energy sources, including that involved in the nature, processing and utilization of coal, petroleum, oil shale, natural gas, biomass and synfuels, as well as related subjects of increasing interest such as C1 chemistry, pollutions control and new catalytic materials. Types of publications include original research articles, short communications, research notes and reviews. Both domestic and international contributors are welcome. Manuscripts written in Chinese or English will be accepted. Additional English titles, abstracts and key words should be included in Chinese manuscripts. All manuscripts are subject to critical review by the editorial committee, which is composed of about 10 foreign and 50 Chinese experts in fuel science. Journal of Fuel Chemistry and Technology has been a source of primary research work in fuel chemistry as a Chinese core scientific periodical.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信