Evolution of Char Structure During In-Situ Biomass Tar Reforming: Importance of the Coupling Effect Among the Physical-Chemical Structure of Char-Based Catalysts

Yu Zhang, D. Feng, Yijun Zhao, Heming Dong, Guozhang Chang, C. Quan, Shaozeng Sun, Yukun Qin
{"title":"Evolution of Char Structure During In-Situ Biomass Tar Reforming: Importance of the Coupling Effect Among the Physical-Chemical Structure of Char-Based Catalysts","authors":"Yu Zhang, D. Feng, Yijun Zhao, Heming Dong, Guozhang Chang, C. Quan, Shaozeng Sun, Yukun Qin","doi":"10.3390/catal9090711","DOIUrl":null,"url":null,"abstract":"In order to illustrate the importance of a coupling effect in the physical-chemical structure of char-based catalysts on in-situ biomass tar reforming, three typical char-based catalysts (graphite, Zhundong coal char, and sawdust biochar) were studied in the fixed-bed/fluidized-bed reactor. The physical-chemical properties of carbon-based catalysts associated with their catalytic abilities were characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), Raman, X-ray photoelectron spectroscopy (XPS), scanning electron microscope–energy dispersive spectrometer (SEM-EDS) and N2 adsorption. The relationship between the specific reactivity and tar reforming ability of carbon-based catalysts was discussed through a micro fluidized bed reaction analyzer (MFBRA–MR). The results indicate that the char-based catalyst has a certain removal ability for in-situ biomass tar of corn straw in an inert atmosphere, which is as follows: sawdust biochar > Zhundong (ZD) coal char > graphite. During the in-situ tar reforming, the alkali and alkaline earth metal species (AAEMs) act as adsorption/reaction sites, affecting the evolution of the aromatic ring structure and oxygen-containing functional groups of the char-based catalyst, and also its pore structure. AAEM species on the surface of char-based catalysts are the active sites for tar reforming, which promotes the increase of active intermediates (C-O bond and C-O-AAEMs), and enhances the interactions between char-based catalysts and biomass tar. The abundant AAEMs may lead to the conversion of O=C–O and C=O to C–O. For tar reforming, the internal pore structure of char-based catalysts is little changed, mainly with the carbon deposit forming on the surface pore structure. The carbon deposit from the reformation of straw tar on the char surface has better reactivity than the inherent carbon structure of ZD coal char and sawdust biochar. There is a positive relationship between the MFBRA–MR specific reactivity and tar catalytic reforming ability of char-based catalysts (decided by the coupling effect in their physical-chemical structure), which can be used to determine the catalytic ability of char-based catalysts on tar reforming directly.","PeriodicalId":209884,"journal":{"name":"Prime Archives in Chemistry","volume":"13 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prime Archives in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/catal9090711","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19

Abstract

In order to illustrate the importance of a coupling effect in the physical-chemical structure of char-based catalysts on in-situ biomass tar reforming, three typical char-based catalysts (graphite, Zhundong coal char, and sawdust biochar) were studied in the fixed-bed/fluidized-bed reactor. The physical-chemical properties of carbon-based catalysts associated with their catalytic abilities were characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), Raman, X-ray photoelectron spectroscopy (XPS), scanning electron microscope–energy dispersive spectrometer (SEM-EDS) and N2 adsorption. The relationship between the specific reactivity and tar reforming ability of carbon-based catalysts was discussed through a micro fluidized bed reaction analyzer (MFBRA–MR). The results indicate that the char-based catalyst has a certain removal ability for in-situ biomass tar of corn straw in an inert atmosphere, which is as follows: sawdust biochar > Zhundong (ZD) coal char > graphite. During the in-situ tar reforming, the alkali and alkaline earth metal species (AAEMs) act as adsorption/reaction sites, affecting the evolution of the aromatic ring structure and oxygen-containing functional groups of the char-based catalyst, and also its pore structure. AAEM species on the surface of char-based catalysts are the active sites for tar reforming, which promotes the increase of active intermediates (C-O bond and C-O-AAEMs), and enhances the interactions between char-based catalysts and biomass tar. The abundant AAEMs may lead to the conversion of O=C–O and C=O to C–O. For tar reforming, the internal pore structure of char-based catalysts is little changed, mainly with the carbon deposit forming on the surface pore structure. The carbon deposit from the reformation of straw tar on the char surface has better reactivity than the inherent carbon structure of ZD coal char and sawdust biochar. There is a positive relationship between the MFBRA–MR specific reactivity and tar catalytic reforming ability of char-based catalysts (decided by the coupling effect in their physical-chemical structure), which can be used to determine the catalytic ability of char-based catalysts on tar reforming directly.
原位生物质焦油重整过程中炭结构的演化:炭基催化剂物理化学结构耦合效应的重要性
为了说明炭基催化剂的物理化学结构耦合效应对原位生物质焦油重整的重要性,在固定床/流化床反应器中对3种典型的炭基催化剂(石墨、准东煤焦和木屑生物炭)进行了研究。采用电感耦合等离子体原子发射光谱(ICP-AES)、拉曼光谱(Raman)、x射线光电子能谱(XPS)、扫描电镜-能谱仪(SEM-EDS)和N2吸附等方法对碳基催化剂的理化性质及其催化性能进行了表征。采用微流化床反应分析仪(MFBRA-MR)研究了碳基催化剂的比反应活性与焦油重整能力之间的关系。结果表明:在惰性气氛下,炭基催化剂对玉米秸秆原位生物质焦油具有一定的脱除能力,脱除效果为:木屑生物炭>准东(ZD)煤炭>石墨。在原位焦油重整过程中,碱和碱土金属(AAEMs)作为吸附/反应位点,影响了炭基催化剂芳香环结构和含氧官能团的演化,也影响了炭基催化剂的孔隙结构。炭基催化剂表面的AAEM物质是焦油重整的活性位点,促进了活性中间体(C-O键和C-O-AAEM)的增加,增强了炭基催化剂与生物质焦油之间的相互作用。大量的aaem可能导致O=C - O和C=O向C - O转化。对于焦油重整,炭基催化剂的内部孔隙结构变化不大,主要是在表面孔隙结构上形成积碳。秸秆焦油重整后炭表面沉积的碳比ZD煤焦和木屑生物炭的固有碳结构具有更好的反应性。炭基催化剂的MFBRA-MR比反应活性与焦油催化重整能力之间存在正相关关系(由其物理-化学结构的耦合效应决定),可直接确定炭基催化剂对焦油重整的催化能力。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信