操作条件对铁催化CO2气化生物炭动力学的影响

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED
D. Chaos-Hernández, N. Latorre, P. Tarifa, E. Romeo, A. Monzón
{"title":"操作条件对铁催化CO2气化生物炭动力学的影响","authors":"D. Chaos-Hernández,&nbsp;N. Latorre,&nbsp;P. Tarifa,&nbsp;E. Romeo,&nbsp;A. Monzón","doi":"10.1016/j.cattod.2025.115289","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, we investigated the catalytic gasification of cellulose-derived biocarbons (CDC) with CO₂ using Fe as the catalyst. Fe(%wt)/CDC samples were synthesized through controlled pyrolysis of cellulose impregnated with iron precursors and evaluated under varying reaction temperatures and CO₂ concentrations. Characterization by XRD, TGA, Raman, TEM, and N₂ adsorption revealed that the initial Fe loading in cellulose not only determines the final carbon content in each Fe(%wt)/CDC sample but also plays a crucial role in regulating the textural and structural properties of the resulting carbonaceous materials, as well as the Fe nanoparticle size distribution. Specifically, higher Fe loading led to a decrease in surface area, reduction of microporosity, an increase of pore diameter, and to larger average Fe nanoparticle sizes. During gasification, Fe nanoparticles were oxidized by CO₂, resulting in a decline in catalytic activity and ultimately limiting the complete gasification of the carbonaceous material by the end of the reaction. These opposing effects explain the varying behaviour observed in the Fe(%wt)/CDC samples studied. Analysis of the initial gasification rates indicated that both, the apparent reaction order with respect to CO₂ and the activation energy, increased with reaction temperature and CO₂ partial pressure (p<sub>CO₂</sub>), respectively. These results were successfully interpreted using a Langmuir-Hinshelwood model, which accounts for the influence of CO₂ adsorption on the observed reaction rate. These findings underscore the potential of Fe(%wt)/CDC materials for CO₂ utilization and biomass valorisation, providing valuable insights for the development of efficient catalytic gasification processes.</div></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"454 ","pages":"Article 115289"},"PeriodicalIF":5.2000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Influence of operating conditions on the kinetics of Iron-catalysed gasification of biocarbons with CO2\",\"authors\":\"D. Chaos-Hernández,&nbsp;N. Latorre,&nbsp;P. Tarifa,&nbsp;E. Romeo,&nbsp;A. Monzón\",\"doi\":\"10.1016/j.cattod.2025.115289\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, we investigated the catalytic gasification of cellulose-derived biocarbons (CDC) with CO₂ using Fe as the catalyst. Fe(%wt)/CDC samples were synthesized through controlled pyrolysis of cellulose impregnated with iron precursors and evaluated under varying reaction temperatures and CO₂ concentrations. Characterization by XRD, TGA, Raman, TEM, and N₂ adsorption revealed that the initial Fe loading in cellulose not only determines the final carbon content in each Fe(%wt)/CDC sample but also plays a crucial role in regulating the textural and structural properties of the resulting carbonaceous materials, as well as the Fe nanoparticle size distribution. Specifically, higher Fe loading led to a decrease in surface area, reduction of microporosity, an increase of pore diameter, and to larger average Fe nanoparticle sizes. During gasification, Fe nanoparticles were oxidized by CO₂, resulting in a decline in catalytic activity and ultimately limiting the complete gasification of the carbonaceous material by the end of the reaction. These opposing effects explain the varying behaviour observed in the Fe(%wt)/CDC samples studied. Analysis of the initial gasification rates indicated that both, the apparent reaction order with respect to CO₂ and the activation energy, increased with reaction temperature and CO₂ partial pressure (p<sub>CO₂</sub>), respectively. These results were successfully interpreted using a Langmuir-Hinshelwood model, which accounts for the influence of CO₂ adsorption on the observed reaction rate. These findings underscore the potential of Fe(%wt)/CDC materials for CO₂ utilization and biomass valorisation, providing valuable insights for the development of efficient catalytic gasification processes.</div></div>\",\"PeriodicalId\":264,\"journal\":{\"name\":\"Catalysis Today\",\"volume\":\"454 \",\"pages\":\"Article 115289\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Today\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0920586125001075\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586125001075","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

摘要

在本研究中,我们研究了以铁为催化剂,用CO₂催化气化纤维素衍生生物碳(CDC)。通过对铁前驱体浸渍纤维素的控制热解合成Fe(%wt)/CDC样品,并在不同的反应温度和CO₂浓度下进行了评价。通过XRD, TGA, Raman, TEM和N₂吸附等表征表明,纤维素中初始铁负载不仅决定了每个Fe(%wt)/CDC样品的最终碳含量,而且对所得到的碳质材料的结构和结构性能以及铁纳米颗粒的分布起着至关重要的调节作用。具体而言,高铁负载导致比表面积减小,微孔隙度减小,孔径增大,平均铁纳米颗粒尺寸增大。在气化过程中,Fe纳米颗粒被CO₂氧化,导致催化活性下降,最终限制了反应结束时碳质材料的完全气化。这些相反的效应解释了在所研究的Fe(%wt)/CDC样品中观察到的不同行为。初始气化速率分析表明,随着反应温度和CO 2分压的升高,CO 2的表观反应阶数和活化能均增加。使用Langmuir-Hinshelwood模型成功地解释了这些结果,该模型解释了CO₂吸附对观察到的反应速率的影响。这些发现强调了Fe(%wt)/CDC材料在CO₂利用和生物质增值方面的潜力,为开发高效催化气化工艺提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of operating conditions on the kinetics of Iron-catalysed gasification of biocarbons with CO2
In this study, we investigated the catalytic gasification of cellulose-derived biocarbons (CDC) with CO₂ using Fe as the catalyst. Fe(%wt)/CDC samples were synthesized through controlled pyrolysis of cellulose impregnated with iron precursors and evaluated under varying reaction temperatures and CO₂ concentrations. Characterization by XRD, TGA, Raman, TEM, and N₂ adsorption revealed that the initial Fe loading in cellulose not only determines the final carbon content in each Fe(%wt)/CDC sample but also plays a crucial role in regulating the textural and structural properties of the resulting carbonaceous materials, as well as the Fe nanoparticle size distribution. Specifically, higher Fe loading led to a decrease in surface area, reduction of microporosity, an increase of pore diameter, and to larger average Fe nanoparticle sizes. During gasification, Fe nanoparticles were oxidized by CO₂, resulting in a decline in catalytic activity and ultimately limiting the complete gasification of the carbonaceous material by the end of the reaction. These opposing effects explain the varying behaviour observed in the Fe(%wt)/CDC samples studied. Analysis of the initial gasification rates indicated that both, the apparent reaction order with respect to CO₂ and the activation energy, increased with reaction temperature and CO₂ partial pressure (pCO₂), respectively. These results were successfully interpreted using a Langmuir-Hinshelwood model, which accounts for the influence of CO₂ adsorption on the observed reaction rate. These findings underscore the potential of Fe(%wt)/CDC materials for CO₂ utilization and biomass valorisation, providing valuable insights for the development of efficient catalytic gasification processes.
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
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.
×
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