合成四面体配位 CoO,直接利用合成气合成高级醇类

IF 4.3 3区 工程技术 Q2 ENGINEERING, CHEMICAL
Zhuoshi Li, Han Yang, Xiaofeng Pei, Jiahui Li, Jing Lv, Shouying Huang, Yue Wang, Xinbin Ma
{"title":"合成四面体配位 CoO,直接利用合成气合成高级醇类","authors":"Zhuoshi Li,&nbsp;Han Yang,&nbsp;Xiaofeng Pei,&nbsp;Jiahui Li,&nbsp;Jing Lv,&nbsp;Shouying Huang,&nbsp;Yue Wang,&nbsp;Xinbin Ma","doi":"10.1007/s11705-024-2448-7","DOIUrl":null,"url":null,"abstract":"<div><p>Higher alcohol synthesis directly from syngas is highly desirable as one of the efficient non-petroleum energy conversion routes. Co<sup>0</sup>–CoO catalysts showed great potential for this reaction, but the alcohol selectivity still needs to be improved and the crystal structure effect of CoO on catalytic behaviors lacks investigation. Here, a series of tetrahedrally coordinated CoO polymorphs were prepared by a thermal decomposition method, which consisted of wurtzite CoO and zinc blende CoO with varied contents. After diluting with SiO<sub>2</sub>, the catalyst showed excellent performance for higher alcohol synthesis with ROH selectivity of 45.8% and higher alcohol distribution of 84.1 wt % under the CO conversion of 38.0%. With increasing the content of wurtzite CoO, the Co<sup>0</sup>/Co<sup>2+</sup> ratio gradually increased in the spent catalysts, while the proportion of highly active hexagonal close packed cobalt in Co<sup>0</sup> decreased, leading to first decreased then increased CO conversion. Moreover, the higher content of zinc blende CoO in fresh catalyst facilitated the retention of more Co<sup>2+</sup> sites in spent catalysts, promoting the ROH selectivity but slightly decreasing the distribution of higher alcohols. The catalyst with 40% wurtzite CoO obtained the optimal performance with a space time yield toward higher alcohols of 7.9 mmol·g<sub>cat</sub><sup>−1</sup>·h<sup>−1</sup>.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":571,"journal":{"name":"Frontiers of Chemical Science and Engineering","volume":"18 8","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of tetrahedrally coordinated CoO for higher alcohol synthesis directly from syngas\",\"authors\":\"Zhuoshi Li,&nbsp;Han Yang,&nbsp;Xiaofeng Pei,&nbsp;Jiahui Li,&nbsp;Jing Lv,&nbsp;Shouying Huang,&nbsp;Yue Wang,&nbsp;Xinbin Ma\",\"doi\":\"10.1007/s11705-024-2448-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Higher alcohol synthesis directly from syngas is highly desirable as one of the efficient non-petroleum energy conversion routes. Co<sup>0</sup>–CoO catalysts showed great potential for this reaction, but the alcohol selectivity still needs to be improved and the crystal structure effect of CoO on catalytic behaviors lacks investigation. Here, a series of tetrahedrally coordinated CoO polymorphs were prepared by a thermal decomposition method, which consisted of wurtzite CoO and zinc blende CoO with varied contents. After diluting with SiO<sub>2</sub>, the catalyst showed excellent performance for higher alcohol synthesis with ROH selectivity of 45.8% and higher alcohol distribution of 84.1 wt % under the CO conversion of 38.0%. With increasing the content of wurtzite CoO, the Co<sup>0</sup>/Co<sup>2+</sup> ratio gradually increased in the spent catalysts, while the proportion of highly active hexagonal close packed cobalt in Co<sup>0</sup> decreased, leading to first decreased then increased CO conversion. Moreover, the higher content of zinc blende CoO in fresh catalyst facilitated the retention of more Co<sup>2+</sup> sites in spent catalysts, promoting the ROH selectivity but slightly decreasing the distribution of higher alcohols. The catalyst with 40% wurtzite CoO obtained the optimal performance with a space time yield toward higher alcohols of 7.9 mmol·g<sub>cat</sub><sup>−1</sup>·h<sup>−1</sup>.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":571,\"journal\":{\"name\":\"Frontiers of Chemical Science and Engineering\",\"volume\":\"18 8\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers of Chemical Science and Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11705-024-2448-7\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers of Chemical Science and Engineering","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s11705-024-2448-7","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

摘要

直接从合成气中合成高级醇是非常理想的高效非石油能源转化途径之一。Co0-CoO 催化剂在这一反应中显示出巨大的潜力,但酒精选择性仍有待提高,CoO 晶体结构对催化行为的影响也缺乏研究。本文采用热分解法制备了一系列四面体配位的 CoO 多晶体,包括不同含量的钨锌钴和锌混钴。用二氧化硅稀释后,催化剂在合成高级醇方面表现出优异的性能,在 CO 转化率为 38.0% 的情况下,ROH 选择性为 45.8%,高级醇分配率为 84.1 wt%。随着孔雀石状 CoO 含量的增加,废催化剂中 Co0/Co2+ 的比例逐渐增加,而 Co0 中高活性六方紧密堆积钴的比例降低,导致 CO 转化率先降后升。此外,新鲜催化剂中混合锌 CoO 含量较高,有利于在废催化剂中保留更多的 Co2+ 位点,从而提高了 ROH 的选择性,但略微降低了高级醇的分布。含 40% wurtzite CoO 的催化剂性能最佳,对高级醇的时空产率为 7.9 mmol-gcat-1-h-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of tetrahedrally coordinated CoO for higher alcohol synthesis directly from syngas

Synthesis of tetrahedrally coordinated CoO for higher alcohol synthesis directly from syngas

Higher alcohol synthesis directly from syngas is highly desirable as one of the efficient non-petroleum energy conversion routes. Co0–CoO catalysts showed great potential for this reaction, but the alcohol selectivity still needs to be improved and the crystal structure effect of CoO on catalytic behaviors lacks investigation. Here, a series of tetrahedrally coordinated CoO polymorphs were prepared by a thermal decomposition method, which consisted of wurtzite CoO and zinc blende CoO with varied contents. After diluting with SiO2, the catalyst showed excellent performance for higher alcohol synthesis with ROH selectivity of 45.8% and higher alcohol distribution of 84.1 wt % under the CO conversion of 38.0%. With increasing the content of wurtzite CoO, the Co0/Co2+ ratio gradually increased in the spent catalysts, while the proportion of highly active hexagonal close packed cobalt in Co0 decreased, leading to first decreased then increased CO conversion. Moreover, the higher content of zinc blende CoO in fresh catalyst facilitated the retention of more Co2+ sites in spent catalysts, promoting the ROH selectivity but slightly decreasing the distribution of higher alcohols. The catalyst with 40% wurtzite CoO obtained the optimal performance with a space time yield toward higher alcohols of 7.9 mmol·gcat−1·h−1.

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
CiteScore
7.60
自引率
6.70%
发文量
868
审稿时长
1 months
期刊介绍: Frontiers of Chemical Science and Engineering presents the latest developments in chemical science and engineering, emphasizing emerging and multidisciplinary fields and international trends in research and development. The journal promotes communication and exchange between scientists all over the world. The contents include original reviews, research papers and short communications. Coverage includes catalysis and reaction engineering, clean energy, functional material, nanotechnology and nanoscience, biomaterials and biotechnology, particle technology and multiphase processing, separation science and technology, sustainable technologies and green processing.
×
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