Coke evolution study in a liquid atomization into gas-solid fluidized bed to convert fructose to value-added chemicals

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-08-10 DOI:10.1016/j.cattod.2024.114972
Zahra Khani , Marine Porte , Joshua Brinkerhoff , Gregory S. Patience
{"title":"Coke evolution study in a liquid atomization into gas-solid fluidized bed to convert fructose to value-added chemicals","authors":"Zahra Khani ,&nbsp;Marine Porte ,&nbsp;Joshua Brinkerhoff ,&nbsp;Gregory S. Patience","doi":"10.1016/j.cattod.2024.114972","DOIUrl":null,"url":null,"abstract":"<div><p>Glucose and fructose are valuable compounds, which have the potential to displace fossil fuels as a feedstock for highly valued products. One of the promising reactions is the oxi-dehydration of fructose to produce Hydroxymethylfurfural, 2,5-diformylfuran, and furfural. Current processes to produce platform chemicals like Hydroxymethylfurfural, furfural, and 2,5-diformylfuran operate in liquid phase with homogeneous heterogeneous catalyst, but commercialization is limited by scale and environmental impact of the large volume solvent required. Here we developed a gas-phase process to convert fructose in a fluidized bed reactor over Mo − V − WO<sub>3</sub>/TiO<sub>2</sub>. However, in the catalytic oxi-dehydration of fructose, coke forms on active sites and decreases conversion but increases selectivity. Coke and reactor performance depends on fructose concentration and O<sub>2</sub>/fructose ratio. In the first 2 h, acidic amorphous coke accumulates (based on TPO, FTIR, and UV–vis). Feeding excess O<sub>2</sub> maintains coke in an amorphous structure and liberates oxide sites. Whereas coke promotes, water block active site reducing yield. In this work, we optimized the operating parameters of fructose concentration (%) and O<sub>2</sub>/fructose ratio, while simultaneously mitigating the issues associated with coke formation and its detrimental effects.</p></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"444 ","pages":"Article 114972"},"PeriodicalIF":5.2000,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0920586124004668/pdfft?md5=baa42eaa8ff22b0ac142b7ce1b3d8a49&pid=1-s2.0-S0920586124004668-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586124004668","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Glucose and fructose are valuable compounds, which have the potential to displace fossil fuels as a feedstock for highly valued products. One of the promising reactions is the oxi-dehydration of fructose to produce Hydroxymethylfurfural, 2,5-diformylfuran, and furfural. Current processes to produce platform chemicals like Hydroxymethylfurfural, furfural, and 2,5-diformylfuran operate in liquid phase with homogeneous heterogeneous catalyst, but commercialization is limited by scale and environmental impact of the large volume solvent required. Here we developed a gas-phase process to convert fructose in a fluidized bed reactor over Mo − V − WO3/TiO2. However, in the catalytic oxi-dehydration of fructose, coke forms on active sites and decreases conversion but increases selectivity. Coke and reactor performance depends on fructose concentration and O2/fructose ratio. In the first 2 h, acidic amorphous coke accumulates (based on TPO, FTIR, and UV–vis). Feeding excess O2 maintains coke in an amorphous structure and liberates oxide sites. Whereas coke promotes, water block active site reducing yield. In this work, we optimized the operating parameters of fructose concentration (%) and O2/fructose ratio, while simultaneously mitigating the issues associated with coke formation and its detrimental effects.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
将果糖转化为增值化学品的液态雾化气固流化床中的焦炭演变研究
葡萄糖和果糖是有价值的化合物,有可能取代化石燃料,成为生产高价值产品的原料。其中一个很有前景的反应是通过果糖的氧脱水反应生产羟甲基糠醛、2,5-二甲酰呋喃和糠醛。目前生产羟甲基糠醛、糠醛和 2,5-二甲酰基呋喃等平台化学品的工艺是在液相中使用均相异相催化剂进行的,但商业化受到规模和所需大量溶剂对环境影响的限制。在此,我们开发了一种气相工艺,在流化床反应器中通过 Mo - V - WO3/TiO2 转化果糖。然而,在果糖的催化氧脱水过程中,焦炭会在活性位点上形成,从而降低转化率,但会提高选择性。焦炭和反应器性能取决于果糖浓度和氧气/果糖比率。在最初的 2 小时内,会积累酸性无定形焦炭(基于 TPO、傅立叶变换红外光谱和紫外可见光)。过量的氧气会使焦炭保持无定形结构,并释放出氧化物位点。焦炭会促进活性位点,而水则会阻塞活性位点,降低产率。在这项工作中,我们优化了果糖浓度(%)和氧气/果糖比率的操作参数,同时减轻了与焦炭形成及其不利影响相关的问题。
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 去求助
来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
期刊最新文献
The peculiar role of copper in the saccharides hydrogenation in aqueous phase Editorial Board Establishing the oxygen evolution reaction pathway on iron-oxy-hydroxide through electro-kinetic study Sulfur-doped carbon/TiO2 composites for ethylene photo-oxidation. Enhanced performance by doping TiO2 phases with sulfur by mobile species inserted on the carbon support Tetravalent metals modulated Zn-based layered double hydroxides and their mixed metal oxides for catalytic depolymerization of carbonyl-coordinating plastic waste
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1