Co/SBA-15催化剂上的费托合成:表征和寡聚化模拟

V. Menezes, G. M. Paula, L. A. Lima, M. Rodrigues, F. Fernandes
{"title":"Co/SBA-15催化剂上的费托合成:表征和寡聚化模拟","authors":"V. Menezes, G. M. Paula, L. A. Lima, M. Rodrigues, F. Fernandes","doi":"10.21926/cr.2203023","DOIUrl":null,"url":null,"abstract":"In this study, we investigated the oligomerization mechanism of the Fischer-Tropsch synthesis catalyzed by a cobalt-based catalyst supported by SBA-15. The Co/SBA-15 catalyst contained 20% w/w of cobalt. It was prepared by the wet impregnation method and characterized by X-ray diffraction (XRD), N2 adsorption-desorption, temperature-programmed reduction (TPR), and scanning electron microscopy coupled to X-ray energy dispersion spectroscopy (SEM-EDS). The FT synthesis was conducted in a slurry bed reactor operating at 240–270°C, 2.0–3.0 MPa, and 1:1–2:1 H2:CO ratio (mol:mol). An oligomerization model, based on alkyl and alkenyl mechanisms for hydrocarbon chain propagation, was used for product distribution. Impregnation with cobalt and calcination did not alter the structure of SBA-15. Cobalt oxides, including Co2O3 and Co3O4, were the active phases of the reaction. Adding cobalt to the support lowered the specific surface area and the pore volume of the support but did not change the structure of SBA-15. Fischer-Tropsch synthesis and C5+ hydrocarbon selectivity increased at a low H2:CO ratio (1.0) and low temperatures (240–255°C). The content of branched-chain paraffin and olefins increased with a decrease in the H2:CO ratio and temperature. The parameters of the model were estimated, and the assumption of a dual mechanism was satisfied.","PeriodicalId":178524,"journal":{"name":"Catalysis Research","volume":"195 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fischer-Tropsch Synthesis on Co/SBA-15 Catalyst: Characterization and Oligomerization Modeling\",\"authors\":\"V. Menezes, G. M. Paula, L. A. Lima, M. Rodrigues, F. Fernandes\",\"doi\":\"10.21926/cr.2203023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, we investigated the oligomerization mechanism of the Fischer-Tropsch synthesis catalyzed by a cobalt-based catalyst supported by SBA-15. The Co/SBA-15 catalyst contained 20% w/w of cobalt. It was prepared by the wet impregnation method and characterized by X-ray diffraction (XRD), N2 adsorption-desorption, temperature-programmed reduction (TPR), and scanning electron microscopy coupled to X-ray energy dispersion spectroscopy (SEM-EDS). The FT synthesis was conducted in a slurry bed reactor operating at 240–270°C, 2.0–3.0 MPa, and 1:1–2:1 H2:CO ratio (mol:mol). An oligomerization model, based on alkyl and alkenyl mechanisms for hydrocarbon chain propagation, was used for product distribution. Impregnation with cobalt and calcination did not alter the structure of SBA-15. Cobalt oxides, including Co2O3 and Co3O4, were the active phases of the reaction. Adding cobalt to the support lowered the specific surface area and the pore volume of the support but did not change the structure of SBA-15. Fischer-Tropsch synthesis and C5+ hydrocarbon selectivity increased at a low H2:CO ratio (1.0) and low temperatures (240–255°C). The content of branched-chain paraffin and olefins increased with a decrease in the H2:CO ratio and temperature. The parameters of the model were estimated, and the assumption of a dual mechanism was satisfied.\",\"PeriodicalId\":178524,\"journal\":{\"name\":\"Catalysis Research\",\"volume\":\"195 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-05-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21926/cr.2203023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21926/cr.2203023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在这项研究中,我们研究了SBA-15负载的钴基催化剂催化费托合成的寡聚化机理。Co/SBA-15催化剂的钴含量为20% w/w。采用湿浸渍法制备,通过x射线衍射(XRD)、N2吸附-解吸、程序升温还原(TPR)、扫描电镜- x射线能谱(SEM-EDS)等手段对其进行表征。在料浆床反应器中,在240 ~ 270℃,2.0 ~ 3.0 MPa, 1:1 ~ 2:1 H2:CO比(mol:mol)条件下合成FT。产品分布采用基于烷基和烯基机制的低聚化模型。钴浸渍和煅烧均未改变SBA-15的结构。Co2O3和Co3O4是反应的活性相。在支架中添加钴降低了支架的比表面积和孔隙体积,但没有改变SBA-15的结构。在较低的H2:CO比(1.0)和较低的温度(240 ~ 255℃)下,费托合成和C5+碳氢化合物选择性提高。支链烷烃和烯烃的含量随着H2:CO比和温度的降低而增加。对模型参数进行了估计,满足双机构的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Fischer-Tropsch Synthesis on Co/SBA-15 Catalyst: Characterization and Oligomerization Modeling
In this study, we investigated the oligomerization mechanism of the Fischer-Tropsch synthesis catalyzed by a cobalt-based catalyst supported by SBA-15. The Co/SBA-15 catalyst contained 20% w/w of cobalt. It was prepared by the wet impregnation method and characterized by X-ray diffraction (XRD), N2 adsorption-desorption, temperature-programmed reduction (TPR), and scanning electron microscopy coupled to X-ray energy dispersion spectroscopy (SEM-EDS). The FT synthesis was conducted in a slurry bed reactor operating at 240–270°C, 2.0–3.0 MPa, and 1:1–2:1 H2:CO ratio (mol:mol). An oligomerization model, based on alkyl and alkenyl mechanisms for hydrocarbon chain propagation, was used for product distribution. Impregnation with cobalt and calcination did not alter the structure of SBA-15. Cobalt oxides, including Co2O3 and Co3O4, were the active phases of the reaction. Adding cobalt to the support lowered the specific surface area and the pore volume of the support but did not change the structure of SBA-15. Fischer-Tropsch synthesis and C5+ hydrocarbon selectivity increased at a low H2:CO ratio (1.0) and low temperatures (240–255°C). The content of branched-chain paraffin and olefins increased with a decrease in the H2:CO ratio and temperature. The parameters of the model were estimated, and the assumption of a dual mechanism was satisfied.
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
自引率
0.00%
发文量
0
期刊最新文献
Effective Photogeneration of Singlet Oxygen and High Photocatalytic and Antibacterial Activities of Porous Mn-Doped ZnO-ZrO2 Nanocomposites Determination of Reflectance Spectra and Colorimetry of Titanium and Tungsten Oxides Obtained by Microwave-assisted Hydrothermal Synthesis A Remarkable Pt Doped CNT Catalyst as a Double Functional Material: Its Application for Hydrogen Production and Supercapacitor NaY Zeolite Synthesis from Vermiculite and Modification with Surfactant Synthesis of SAPO-34 Zeolite Membrane: Influence of Sources of Silica
×
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