Title of article :
Investigation of Oxidative Desulfurization of Light Naphtha by NiMo/𝛾-Al2O3 Catalyst
Author/Authors :
Sheibani ، Soheila Department of Chemistry - Islamic Azad University, Science and Research Branch , Zare ، Karim Department of Chemistry - Islamic Azad University, Science and Research Branch , Mousavi-Safavi ، Mahmoud Islamic Azad University, Buin Zahra Branch
From page :
417
To page :
427
Abstract :
In this research, we investigated the effects of parameters, including reaction time, reaction temperature, the mass ratio (mcat./mfeed), and volume ratio (VH2O2/Vfeed) on sulfur removal conversion of light naphtha under oxidative desulfurization (ODS) reaction. So to achieve this goal, several active catalysts are prepared while molybdenum (Mo) was used as an active metal. Nickel (Ni) was the promoter. 𝛾-alumina (𝛾-Al2O3) was used as a support and modified by chelate agents such as citric acid (C6H8O7), ethylene diamine tetra acetic acid (EDTA), polyethylene glycol (PEG), Sorbitol, and urea ((NH4)2CO). These catalysts were synthesized by using the wetness impregnation in-situ method. Then they were applied to the ODS process for light naphtha. These catalysts were characterized by N2-adsorbtion desorption isotherms (BET, BJH), Scanning Electron Microscope (SEM), temperature-programmed desorption (NH3-TPD), and FT-IR analysis. The catalyst that synthesized in the presence of sorbitol, had the best performance. The optimization conditions for this catalyst were m (catalyst)/m (feed)= 0.013, reaction temperature of 35 °C, 50 mL of feed, 0.5 g of catalyst, 1 hour reaction time, and V (H2O2)/VFeed = 0.045. It revealed the maximum performance for ODS reaction of the real feed. Under these circumstances, the sulfur of light naphtha decreased from 160 ppm to 38 ppm during the reaction.
Keywords :
molybdenum oxide , Nickel oxide , Oxidative desulfurization catalyst , Chelating agent , light naphtha
Journal title :
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Journal title :
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Record number :
2676362
Link To Document :
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