Enhancement of heavy vacuum gas oil desulfurization via using developed catalyst based on Al2O3

Asmaa I. Zahran, A. Naggar, W. A. Aboutaleb, M. A. Sayed, Huda S. Ahmed, Mohamed I A. Mekew
{"title":"Enhancement of heavy vacuum gas oil desulfurization via using developed catalyst based on Al2O3","authors":"Asmaa I. Zahran, A. Naggar, W. A. Aboutaleb, M. A. Sayed, Huda S. Ahmed, Mohamed I A. Mekew","doi":"10.21608/ejchem.2020.24452.2457","DOIUrl":null,"url":null,"abstract":"In past few decades, a strong attention is paid to develop high-active catalysts for hydrotreating of the heavy vacuum gas oil (HVGO). In an agreement with that claim, this research work reports the synthesis of a developed catalyst for desulfurization of a petroleum HVGO fraction. Particularly, the catalytic performance of the catalyst, which was made via addition of CeO2 to ɣ alumina as supports for a trimetallic composite (CoNiMo-Al2O3), toward sulfur removal was investigated. For proper comparison, the activity of alumina individually-supported trimetallic catalyst CoNiMo-ɣAl2O3 at such application was also studied. The as-prepared catalysts were characterized by N2 physical adsorption/desorption (BET), transmission electron microscopy (TEM) and X-ray diffraction (XRD). Catalytic activity was conducted in continuous flow trickle-bed reactor at various operating condition of temperature (320-380 °C), pressure (20-60 bar) and liquid hour space velocity (1-2.5 h-1). It was found that CoNiMo/CeO2-ɣAl2O3 was of a higher catalytic efficiency to hydrotreating of HVGO than that of CoNiMo-Al2O3. Numerically, CoNiMo/CeO2-ɣAl2O3 could successfully remove 83.5 % of sulfur compounds while it was only 66.2% in case of CoNiMo-Al2O3. The increased catalytic performance of ceria containing composite may be due to its high specific surface area (∼198.4 m2·g−1) and small crystallite size (24.24 nm). Moreover, the incorporation of CeO2 to alumina could subsequently inhibit the interaction between Ni and alumina; hence the inactive NiAl2O4 phase had not been formed. Thus, an enhanced catalytic desulfurization process could be attained.","PeriodicalId":22429,"journal":{"name":"The Egyptian Journal of Chemistry","volume":"26 1","pages":"0-0"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Egyptian Journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/ejchem.2020.24452.2457","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

In past few decades, a strong attention is paid to develop high-active catalysts for hydrotreating of the heavy vacuum gas oil (HVGO). In an agreement with that claim, this research work reports the synthesis of a developed catalyst for desulfurization of a petroleum HVGO fraction. Particularly, the catalytic performance of the catalyst, which was made via addition of CeO2 to ɣ alumina as supports for a trimetallic composite (CoNiMo-Al2O3), toward sulfur removal was investigated. For proper comparison, the activity of alumina individually-supported trimetallic catalyst CoNiMo-ɣAl2O3 at such application was also studied. The as-prepared catalysts were characterized by N2 physical adsorption/desorption (BET), transmission electron microscopy (TEM) and X-ray diffraction (XRD). Catalytic activity was conducted in continuous flow trickle-bed reactor at various operating condition of temperature (320-380 °C), pressure (20-60 bar) and liquid hour space velocity (1-2.5 h-1). It was found that CoNiMo/CeO2-ɣAl2O3 was of a higher catalytic efficiency to hydrotreating of HVGO than that of CoNiMo-Al2O3. Numerically, CoNiMo/CeO2-ɣAl2O3 could successfully remove 83.5 % of sulfur compounds while it was only 66.2% in case of CoNiMo-Al2O3. The increased catalytic performance of ceria containing composite may be due to its high specific surface area (∼198.4 m2·g−1) and small crystallite size (24.24 nm). Moreover, the incorporation of CeO2 to alumina could subsequently inhibit the interaction between Ni and alumina; hence the inactive NiAl2O4 phase had not been formed. Thus, an enhanced catalytic desulfurization process could be attained.
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
研制的Al2O3催化剂强化重真空气油脱硫
在过去的几十年里,开发高活性催化剂用于重真空瓦斯油的加氢处理受到了广泛的关注。与该说法一致,本研究工作报告了一种用于石油HVGO馏分脱硫的开发催化剂的合成。特别地,通过在氧化铝上添加CeO2作为三金属复合材料(CoNiMo-Al2O3)的载体,研究了催化剂对硫的催化性能。为了进行适当的比较,还研究了氧化铝单负载三金属催化剂CoNiMo- α Al2O3在这种应用中的活性。采用N2物理吸附/脱附(BET)、透射电镜(TEM)和x射线衍射(XRD)对催化剂进行了表征。在连续流滴床反应器中,在温度(320 ~ 380℃)、压力(20 ~ 60 bar)、液时空速(1 ~ 2.5 h-1)等不同工况下进行催化活性研究。结果表明,CoNiMo/CeO2- Al2O3对HVGO加氢处理的催化效率高于CoNiMo-Al2O3。数值结果表明,CoNiMo/CeO2- Al2O3对硫化物的去除率为83.5%,CoNiMo-Al2O3对硫化物的去除率仅为66.2%。含铈复合材料催化性能的提高可能是由于其高比表面积(~ 198.4 m2·g−1)和小晶粒尺寸(24.24 nm)。此外,CeO2掺入到氧化铝中会抑制Ni与氧化铝之间的相互作用;因此未形成非活性NiAl2O4相。因此,可以获得一个增强的催化脱硫过程。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Synthesis, Characterization and Biological Evaluation of Benzimidazole and Benzindazole Derivatives as Anti-hypertensive Agents Seawater Reinforces Synthesis of Mesoporous and Microporous Zeolites from Egyptian Fly Ash for Removal Ions of Cadmium, Iron, Nickel, and Lead from Artificially Contaminated Water A minireview on Applications of the metal-organic framework and carbon dots in dye photodegradation to protect the aquatic environment from organic pollutants Optimized Synthesis of Biopolymer-Based Zinc Oxide Nanoparticles and Evaluation of Their Antibacterial Activity Metabolic syndrome and the risk of kidney diseases: the impact of life style modification
×
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