Furfural production from the lignocellulosic agro-forestry waste by solvolysis method – A technical review

IF 7.2 2区 工程技术 Q1 CHEMISTRY, APPLIED
Qiaoqiao Zhou , Ajing Ding , Lei Zhang , Jingwei Wang , Jinxing Gu , Ta Yeong Wu , Xuehong Gu , Lian Zhang
{"title":"Furfural production from the lignocellulosic agro-forestry waste by solvolysis method – A technical review","authors":"Qiaoqiao Zhou ,&nbsp;Ajing Ding ,&nbsp;Lei Zhang ,&nbsp;Jingwei Wang ,&nbsp;Jinxing Gu ,&nbsp;Ta Yeong Wu ,&nbsp;Xuehong Gu ,&nbsp;Lian Zhang","doi":"10.1016/j.fuproc.2024.108063","DOIUrl":null,"url":null,"abstract":"<div><p>Furfural is one of the most prospective platform chemicals derived from biomass. This review summarises the principal factors governing the yield/selectivity of furfural by solvolysis technique, with a particular attention to the conversion of C6 cellulose feedstock. So far, most studies focused on the C5 sugar-rich feedstock, which requires solely dehydration to convert into furfural. In contrast, the conversion of C6 sugars to furfural is more challenging, requiring dehydration and C<img>C bond breakage. Depending on the type of biomass and catalyst, the reaction temperature and residence time have an optimum value of ∼160–180 °C and ∼ 30–120 min respectively in traditional heating mode. The low optimum temperature (∼140 °C) for the microwave-assisted technique and that C5 polymers do not necessarily require longer reaction time than their monomers indicate that microwave irradiation is more efficient in depolymerisation reaction of polymers. Additionally, the organic solvent systems containing &lt;10 wt% water were the most promising. For catalysts, sulphates/sulphonated catalysts showed the highest potential for furfural production, and Zn<sup>2+</sup>, Cu<sup>2+</sup> and Fe<sup>3+</sup> are the most promising cationic candidates. Finally, the future perspectives were proposed, including development of novel heterogeneous catalysts and microwave-assisted technique, kinetic study and mechanistic study for the conversion of C6 sugars.</p></div>","PeriodicalId":326,"journal":{"name":"Fuel Processing Technology","volume":"255 ","pages":"Article 108063"},"PeriodicalIF":7.2000,"publicationDate":"2024-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S037838202400033X/pdfft?md5=8903d4c4532866ea2d624da16f2951a5&pid=1-s2.0-S037838202400033X-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Processing Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S037838202400033X","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Furfural is one of the most prospective platform chemicals derived from biomass. This review summarises the principal factors governing the yield/selectivity of furfural by solvolysis technique, with a particular attention to the conversion of C6 cellulose feedstock. So far, most studies focused on the C5 sugar-rich feedstock, which requires solely dehydration to convert into furfural. In contrast, the conversion of C6 sugars to furfural is more challenging, requiring dehydration and CC bond breakage. Depending on the type of biomass and catalyst, the reaction temperature and residence time have an optimum value of ∼160–180 °C and ∼ 30–120 min respectively in traditional heating mode. The low optimum temperature (∼140 °C) for the microwave-assisted technique and that C5 polymers do not necessarily require longer reaction time than their monomers indicate that microwave irradiation is more efficient in depolymerisation reaction of polymers. Additionally, the organic solvent systems containing <10 wt% water were the most promising. For catalysts, sulphates/sulphonated catalysts showed the highest potential for furfural production, and Zn2+, Cu2+ and Fe3+ are the most promising cationic candidates. Finally, the future perspectives were proposed, including development of novel heterogeneous catalysts and microwave-assisted technique, kinetic study and mechanistic study for the conversion of C6 sugars.

Abstract Image

利用溶解法从木质纤维素农林废弃物中生产糠醛 - 技术综述
糠醛是从生物质中提取的最具前景的平台化学品之一。本综述总结了利用溶解技术生产糠醛的产量/选择性的主要影响因素,并特别关注了 C6 纤维素原料的转化问题。迄今为止,大多数研究都集中在富含 C5 糖的原料上,这种原料只需脱水即可转化为糠醛。相比之下,C6 糖转化为糠醛更具挑战性,需要脱水和 CC 键断裂。根据生物质和催化剂的类型,在传统加热模式下,反应温度和停留时间的最佳值分别为 ∼ 160-180 °C 和 ∼ 30-120 分钟。微波辅助技术的最佳温度较低(140 °C),而且 C5 聚合物并不一定需要比其单体更长的反应时间,这表明微波辐照在聚合物的解聚反应中更为有效。此外,含水 10 wt%的有机溶剂体系最有前景。催化剂方面,硫酸盐/磺化催化剂显示出生产糠醛的最大潜力,而 Zn2+、Cu2+ 和 Fe3+ 是最有前途的阳离子候选催化剂。最后,提出了未来的展望,包括开发新型异相催化剂和微波辅助技术、动力学研究和 C6 糖转化的机理研究。
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
Fuel Processing Technology
Fuel Processing Technology 工程技术-工程:化工
CiteScore
13.20
自引率
9.30%
发文量
398
审稿时长
26 days
期刊介绍: Fuel Processing Technology (FPT) deals with the scientific and technological aspects of converting fossil and renewable resources to clean fuels, value-added chemicals, fuel-related advanced carbon materials and by-products. In addition to the traditional non-nuclear fossil fuels, biomass and wastes, papers on the integration of renewables such as solar and wind energy and energy storage into the fuel processing processes, as well as papers on the production and conversion of non-carbon-containing fuels such as hydrogen and ammonia, are also welcome. While chemical conversion is emphasized, papers on advanced physical conversion processes are also considered for publication in FPT. Papers on the fundamental aspects of fuel structure and properties will also be considered.
×
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