Selective cellobiose photoreforming for simultaneous gluconic acid and syngas production in acidic conditions

IF 20.2 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jiu Wang , Heng Zhao , Lin Chen , Jonas Björk , Johanna Rosen , Pawan Kumar , Liquan Jing , Jun Chen , Md Golam Kibria , Jinguang Hu
{"title":"Selective cellobiose photoreforming for simultaneous gluconic acid and syngas production in acidic conditions","authors":"Jiu Wang ,&nbsp;Heng Zhao ,&nbsp;Lin Chen ,&nbsp;Jonas Björk ,&nbsp;Johanna Rosen ,&nbsp;Pawan Kumar ,&nbsp;Liquan Jing ,&nbsp;Jun Chen ,&nbsp;Md Golam Kibria ,&nbsp;Jinguang Hu","doi":"10.1016/j.apcatb.2023.123665","DOIUrl":null,"url":null,"abstract":"<div><p><span>Here, we demonstrate the selective cellobiose (building block of cellulose) photoreforming for gluconic acid and syngas co-production in acidic conditions by rationally designing a bifunctional polymeric carbon nitride<span> (CN) with potassium/sulfur co-dopant. This heteroatomic doped CN photocatalyst possesses enhanced visible light absorption, higher charge separation efficiency than pristine CN. Under acidic conditions, cellobiose is not only more efficiently hydrolyzed into glucose but also promotes the syngas and gluconic acid production. Density functional theory (DFT) calculations reveal the favorable generation of •O</span></span><sub>2</sub><sup>−</sup> during the photocatalytic reaction, which is essential for gluconic acid production. Consequently, the fine-designed photocatalyst presents excellent cellobiose conversion (&gt;80%) and gluconic acid selectivity (&gt;70%) together with the co-production of syngas (∼56 μmol g<sup>−1</sup> h<sup>−1</sup>) under light illumination. The current work demonstrates the feasibility of biomass photoreforming with value-added chemicals and syngas co-production under mild condition.</p></div>","PeriodicalId":244,"journal":{"name":"Applied Catalysis B: Environmental","volume":null,"pages":null},"PeriodicalIF":20.2000,"publicationDate":"2023-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environmental","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926337323013085","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Here, we demonstrate the selective cellobiose (building block of cellulose) photoreforming for gluconic acid and syngas co-production in acidic conditions by rationally designing a bifunctional polymeric carbon nitride (CN) with potassium/sulfur co-dopant. This heteroatomic doped CN photocatalyst possesses enhanced visible light absorption, higher charge separation efficiency than pristine CN. Under acidic conditions, cellobiose is not only more efficiently hydrolyzed into glucose but also promotes the syngas and gluconic acid production. Density functional theory (DFT) calculations reveal the favorable generation of •O2 during the photocatalytic reaction, which is essential for gluconic acid production. Consequently, the fine-designed photocatalyst presents excellent cellobiose conversion (>80%) and gluconic acid selectivity (>70%) together with the co-production of syngas (∼56 μmol g−1 h−1) under light illumination. The current work demonstrates the feasibility of biomass photoreforming with value-added chemicals and syngas co-production under mild condition.

Abstract Image

在酸性条件下同时生产葡萄糖酸和合成气的选择性纤维素生物糖光转化技术
在这里,我们通过合理设计一种带有钾/硫共掺杂剂的双功能聚合物氮化碳(CN),展示了在酸性条件下选择性纤维生物糖(纤维素的组成成分)光催化葡萄糖酸和合成气联产的方法。这种杂原子掺杂的 CN 光催化剂具有更强的可见光吸收能力,电荷分离效率高于原始 CN。在酸性条件下,纤维生物糖不仅能更有效地水解成葡萄糖,还能促进合成气和葡萄糖酸的产生。密度泛函理论(DFT)计算显示,光催化反应过程中有利于生成-O2-,而这对葡萄糖酸的生成至关重要。因此,精细设计的光催化剂具有出色的纤维生物糖转化率(80%)和葡萄糖酸选择性(70%),并能在光照下同时产生合成气(约 56 μmol g-1 h-1)。目前的工作证明了在温和条件下生物质光转化增值化学品和联产合成气的可行性。
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
Applied Catalysis B: Environmental
Applied Catalysis B: Environmental 环境科学-工程:化工
CiteScore
38.60
自引率
6.30%
发文量
1117
审稿时长
24 days
期刊介绍: Applied Catalysis B: Environment and Energy (formerly Applied Catalysis B: Environmental) is a journal that focuses on the transition towards cleaner and more sustainable energy sources. The journal's publications cover a wide range of topics, including: 1.Catalytic elimination of environmental pollutants such as nitrogen oxides, carbon monoxide, sulfur compounds, chlorinated and other organic compounds, and soot emitted from stationary or mobile sources. 2.Basic understanding of catalysts used in environmental pollution abatement, particularly in industrial processes. 3.All aspects of preparation, characterization, activation, deactivation, and regeneration of novel and commercially applicable environmental catalysts. 4.New catalytic routes and processes for the production of clean energy, such as hydrogen generation via catalytic fuel processing, and new catalysts and electrocatalysts for fuel cells. 5.Catalytic reactions that convert wastes into useful products. 6.Clean manufacturing techniques that replace toxic chemicals with environmentally friendly catalysts. 7.Scientific aspects of photocatalytic processes and a basic understanding of photocatalysts as applied to environmental problems. 8.New catalytic combustion technologies and catalysts. 9.New catalytic non-enzymatic transformations of biomass components. The journal is abstracted and indexed in API Abstracts, Research Alert, Chemical Abstracts, Web of Science, Theoretical Chemical Engineering Abstracts, Engineering, Technology & Applied Sciences, and others.
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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