{"title":"Investigation of the effect of catalyst support on oleic acid catalytic deoxygenation for green diesel production","authors":"Mohammed Siraj, Selim Ceylan","doi":"10.1007/s10934-024-01725-2","DOIUrl":null,"url":null,"abstract":"<div><p>The presence of certain oxygenated species has led to the development of green diesel produced using deoxygenation (DO) technology to replace conventional biodiesel. The study focused on the effects of the supports on the deoxygenation of oleic acid using the CoMo catalyst. The results of this study revealed that the Molybdenum and Cobalt species have a significant influence on the reactivity and distribution of the product. The CoMo-based catalyst supported on Cerium oxide (CeO<sub>2</sub>), Titanium dioxide (TiO<sub>2</sub>), activated carbon (AC), and Aluminum oxide (Al<sub>2</sub>O<sub>3</sub>) were prepared by wet impregnation method and then calcinated under 20 mL min<sup>−1</sup> N<sub>2</sub> flow for 4 h at a temperature of 550 °C. The prepared catalysts were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), Thermo-Gravimetric Analysis (TGA), and Scanning Electron Microscopy (SEM) analysis. The influence of support type (activated carbon, Al<sub>2</sub>O<sub>2</sub>, CeO<sub>2</sub>, and TiO<sub>2</sub>) on the removal of various oxygenated functional groups was examined during the deoxygenation of oleic acid using supported CoMo catalysts at 350 °C and atmospheric pressure. The deoxygenated liquid products were characterized by Fourier-transform infrared spectroscopy (FTIR), Gas Chromatography–Mass Spectrometry (GC–MS), Higher heating value (HHV), and CHNOS analysis. The yield of hydrocarbons increased in the order Blank < CoMo/TiO<sub>2</sub> < CoMo/CeO<sub>2</sub> < CoMo/Al<sub>2</sub>O<sub>3</sub> < CoMo/AC. Based on the study results, CoMo/AC is the most active catalyst with 93.20% hydrocarbon yield for 2 h. at 350 °C and 300 rpm in the absence of hydrogen. However, a significant deoxygenation reaction was still observed for the catalysts having CoMo supported on Al<sub>2</sub>O<sub>3</sub>, CeO<sub>2</sub>, and TiO<sub>2</sub>. In summary, CoMo/AC demonstrates better catalytic performance, attributed to its favorable physicochemical properties.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"32 3","pages":"941 - 952"},"PeriodicalIF":3.2000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10934-024-01725-2.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Porous Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10934-024-01725-2","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
The presence of certain oxygenated species has led to the development of green diesel produced using deoxygenation (DO) technology to replace conventional biodiesel. The study focused on the effects of the supports on the deoxygenation of oleic acid using the CoMo catalyst. The results of this study revealed that the Molybdenum and Cobalt species have a significant influence on the reactivity and distribution of the product. The CoMo-based catalyst supported on Cerium oxide (CeO2), Titanium dioxide (TiO2), activated carbon (AC), and Aluminum oxide (Al2O3) were prepared by wet impregnation method and then calcinated under 20 mL min−1 N2 flow for 4 h at a temperature of 550 °C. The prepared catalysts were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), Thermo-Gravimetric Analysis (TGA), and Scanning Electron Microscopy (SEM) analysis. The influence of support type (activated carbon, Al2O2, CeO2, and TiO2) on the removal of various oxygenated functional groups was examined during the deoxygenation of oleic acid using supported CoMo catalysts at 350 °C and atmospheric pressure. The deoxygenated liquid products were characterized by Fourier-transform infrared spectroscopy (FTIR), Gas Chromatography–Mass Spectrometry (GC–MS), Higher heating value (HHV), and CHNOS analysis. The yield of hydrocarbons increased in the order Blank < CoMo/TiO2 < CoMo/CeO2 < CoMo/Al2O3 < CoMo/AC. Based on the study results, CoMo/AC is the most active catalyst with 93.20% hydrocarbon yield for 2 h. at 350 °C and 300 rpm in the absence of hydrogen. However, a significant deoxygenation reaction was still observed for the catalysts having CoMo supported on Al2O3, CeO2, and TiO2. In summary, CoMo/AC demonstrates better catalytic performance, attributed to its favorable physicochemical properties.
期刊介绍:
The Journal of Porous Materials is an interdisciplinary and international periodical devoted to all types of porous materials. Its aim is the rapid publication
of high quality, peer-reviewed papers focused on the synthesis, processing, characterization and property evaluation of all porous materials. The objective is to
establish a unique journal that will serve as a principal means of communication for the growing interdisciplinary field of porous materials.
Porous materials include microporous materials with 50 nm pores.
Examples of microporous materials are natural and synthetic molecular sieves, cationic and anionic clays, pillared clays, tobermorites, pillared Zr and Ti
phosphates, spherosilicates, carbons, porous polymers, xerogels, etc. Mesoporous materials include synthetic molecular sieves, xerogels, aerogels, glasses, glass
ceramics, porous polymers, etc.; while macroporous materials include ceramics, glass ceramics, porous polymers, aerogels, cement, etc. The porous materials
can be crystalline, semicrystalline or noncrystalline, or combinations thereof. They can also be either organic, inorganic, or their composites. The overall
objective of the journal is the establishment of one main forum covering the basic and applied aspects of all porous materials.