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{"title":"The Production of Green Diesel Rich Pentadecane (C15) from Catalytic Hydrodeoxygenation of Waste Cooking Oil using Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2","authors":"Momodou Salieu Sowe, Arda Rista Lestari, Eka Novitasari, M. Masruri, S. M. Ulfa","doi":"10.9767/bcrec.17.1.12700.135-145","DOIUrl":null,"url":null,"abstract":"Hydrodeoxygenation (HDO) is applied in fuel processing technology to convert bio-oils to green diesel with metal-based catalysts. The major challenges to this process are feedstock, catalyst preparation, and the production of oxygen-free diesel fuel. In this study, we aimed to synthesize Ni catalysts supported on silica-zirconia and alumina-zirconia binary oxides and evaluated their catalytic activity for waste cooking oil (WCO) hydrodeoxygenation to green diesel. Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2 were synthesized by wet-impregnation and hydrodeoxygenation of WCO was done using a modified batch reactor. The catalysts were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy - energy dispersive X-ray spectroscopy (SEM-EDS), and N2 isotherm adsorption-desorption analysis. Gas chromatography - mass spectrometry (GC-MS) analysis showed the formation of hydrocarbon framework n-C15 generated from the use of Ni/Al2O3-ZrO2 with the selectivity of 68.97% after a 2 h reaction. Prolonged reaction into 4 h, decreased the selectivity to 58.69%. Ni/SiO2-ZrO2 catalyst at 2 h showed selectivity of 55.39% to n-C15. Conversely, it was observed that the reaction for 4 h increased selectivity to 65.13%. Overall, Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2 catalysts produced oxygen-free green diesel range (n-C14-C18) enriched with n-C15 hydrocarbon. Reaction time influenced the selectivity to n-C15 hydrocarbon. Both catalysts showed promising hydrodeoxygenation activity via the hydrodecarboxylation pathway. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). ","PeriodicalId":46276,"journal":{"name":"Bulletin of Chemical Reaction Engineering and Catalysis","volume":" ","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2021-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Chemical Reaction Engineering and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9767/bcrec.17.1.12700.135-145","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
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Ni/Al2O3-ZrO2和Ni/SiO2-ZrO2催化废食用油加氢脱氧制备富绿色柴油十五烷(C15
氢脱氧(HDO)是一种利用金属基催化剂将生物油转化为绿色柴油的燃料加工技术。该工艺面临的主要挑战是原料、催化剂制备和无氧柴油的生产。本研究旨在合成二氧化硅-二氧化锆和氧化铝-二氧化锆二元氧化物负载的Ni催化剂,并评价其对废食用油加氢脱氧制绿色柴油的催化活性。采用湿浸渍法合成了Ni/Al2O3-ZrO2和Ni/SiO2-ZrO2,并利用改进的间歇式反应器对WCO进行了加氢脱氧。采用x射线衍射(XRD)、x射线荧光(XRF)、扫描电镜- x射线能谱(SEM-EDS)和N2等温吸附-脱附分析对催化剂进行了表征。气相色谱-质谱(GC-MS)分析表明,Ni/Al2O3-ZrO2反应2h后生成的碳氢化合物骨架n-C15的选择性为68.97%。反应时间延长至4 h,选择性降至58.69%。Ni/SiO2-ZrO2催化剂在2 h时对n-C15的选择性为55.39%。相反,反应4 h后,选择性提高到65.13%。总体而言,Ni/Al2O3-ZrO2和Ni/SiO2-ZrO2催化剂产生了富含n-C15烃的无氧绿色柴油(n-C14-C18)。反应时间影响了对n-C15烃的选择性。两种催化剂均通过加氢脱羧途径表现出良好的加氢脱氧活性。版权所有©2021作者,BCREC集团出版。这是一篇基于CC BY-SA许可(https://creativecommons.org/licenses/by-sa/4.0)的开放获取文章。
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