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.