Effect of Ce modification on the performance of CuLDH catalyst for CO2 hydrogenation to methanol

Q3 Energy
Haoran LIU , Zhiqing YU , Wenbin HUANG , Qiang WEI , Peng JIANG , Yasong ZHOU
{"title":"Effect of Ce modification on the performance of CuLDH catalyst for CO2 hydrogenation to methanol","authors":"Haoran LIU ,&nbsp;Zhiqing YU ,&nbsp;Wenbin HUANG ,&nbsp;Qiang WEI ,&nbsp;Peng JIANG ,&nbsp;Yasong ZHOU","doi":"10.1016/S1872-5813(23)60392-5","DOIUrl":null,"url":null,"abstract":"<div><p>A series of Ce modified CuLDH-Ce<sub><em>x</em></sub> catalysts were synthesized by adding different amounts of Ce to CuMgAl hydrotalcite (CuLDH) catalysts. The physicochemical properties of the catalysts were characterized by X-ray diffraction (XRD), N<sub>2</sub> adsorption-desorption (BET), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), etc. The results showed that the addition of Ce changed the hydrotalcite structure of CuLDH catalyst, and an appropriate amount of Ce increased the surface area of the catalyst and improved the dispersion of Cu particles. At the same time, an appropriate amount of Ce was beneficial for increasing the density of strong alkaline sites and the number of oxygen vacancies on the catalyst surface, promoting the adsorption and conversion of CO<sub>2</sub>. Ce was beneficial for adjusting the Cu<sup>+</sup>/Cu<sup>0</sup> ratio on the catalyst surface, and a higher Cu<sup>+</sup>/Cu<sup>0</sup> ratio was conducive to the formation of methanol. When the Ce/Cu ratio was 0.3, the catalyst exhibited higher activity with 7.5% CO<sub>2</sub> conversion, 78.4% methanol selectivity and 362.8 g/(kg·h) spatiotemporal yield at 240 °C under 2.5 MPa with a GHSV=9000 mL/(g·h). It was proved by <em>in-situ</em> DRIFTS that CuLDH-Ce0.3 catalyst followed HCOO* reaction path during CO<sub>2</sub> hydrogenation for methanol.</p></div>","PeriodicalId":15956,"journal":{"name":"燃料化学学报","volume":"52 2","pages":"Pages 159-170"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","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/S1872581323603925","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

Abstract

A series of Ce modified CuLDH-Cex catalysts were synthesized by adding different amounts of Ce to CuMgAl hydrotalcite (CuLDH) catalysts. The physicochemical properties of the catalysts were characterized by X-ray diffraction (XRD), N2 adsorption-desorption (BET), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), etc. The results showed that the addition of Ce changed the hydrotalcite structure of CuLDH catalyst, and an appropriate amount of Ce increased the surface area of the catalyst and improved the dispersion of Cu particles. At the same time, an appropriate amount of Ce was beneficial for increasing the density of strong alkaline sites and the number of oxygen vacancies on the catalyst surface, promoting the adsorption and conversion of CO2. Ce was beneficial for adjusting the Cu+/Cu0 ratio on the catalyst surface, and a higher Cu+/Cu0 ratio was conducive to the formation of methanol. When the Ce/Cu ratio was 0.3, the catalyst exhibited higher activity with 7.5% CO2 conversion, 78.4% methanol selectivity and 362.8 g/(kg·h) spatiotemporal yield at 240 °C under 2.5 MPa with a GHSV=9000 mL/(g·h). It was proved by in-situ DRIFTS that CuLDH-Ce0.3 catalyst followed HCOO* reaction path during CO2 hydrogenation for methanol.

Ce 改性对用于 CO2 加氢制甲醇的 CuLDH 催化剂性能的影响
通过在铜镁铝氢铝酸盐(CuLDH)催化剂中添加不同量的 Ce,合成了一系列 Ce 改性 CuLDH-Cex 催化剂。通过 X 射线衍射 (XRD)、N2 吸附-脱附 (BET)、透射电子显微镜 (TEM)、X 射线光电子能谱 (XPS) 等对催化剂的理化性质进行了表征。结果表明,Ce 的加入改变了 CuLDH 催化剂的氢铝酸盐结构,适量的 Ce 增加了催化剂的比表面积,改善了 Cu 颗粒的分散性。同时,适量的 Ce 有利于增加催化剂表面强碱位点的密度和氧空位的数量,促进 CO2 的吸附和转化。Ce 有利于调节催化剂表面的 Cu+/Cu0 比,较高的 Cu+/Cu0 比有利于甲醇的生成。当 Ce/Cu 比为 0.3 时,催化剂表现出更高的活性,在 240 ℃、2.5 MPa 条件下,二氧化碳转化率为 7.5%,甲醇选择性为 78.4%,时空产率为 362.8 g/(kg-h),GHSV=9000 mL/(g-h)。原位 DRIFTS 证明,CuLDH-Ce0.3 催化剂在 CO2 加氢制甲醇过程中遵循 HCOO* 反应路径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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:481959085
Book学术官方微信