TY - JOUR ID - 37259 TI - The Effects of pH and Chelating Agent on Synthesis and Characterization of Ni Mo/γ- Alumina Nanocatalyst for Heavy Oil Hydrodesulfurization JO - Iranian Journal of Chemistry and Chemical Engineering JA - IJCCE LA - en SN - 1021-9986 AU - Sheibani, Soheila AU - Zare, Karim AU - Mousavi Safavi, Seyed Mahmoud AD - Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran, I.R. IRAN AD - Department of Chemistry and Chemical Engineering, Buin Zahra Branch, Islamic Azad University, Buin Zahra, I.R. IRAN Y1 - 2021 PY - 2021 VL - 40 IS - 1 SP - 21 EP - 34 KW - molybdenum oxide KW - Nickel oxide KW - Nanostructures KW - Hydrodesulfurization KW - Chelating agent KW - Heavy oil DO - 10.30492/ijcce.2019.37259 N2 - In this research, various organic additives (as a chelating agent) were used to prepare NiMo/ 𝛾-Al2O3 bimetallic catalysts. Then effects of additives and pH variation were studied on textural properties, morphology, and size of nanocatalyst particles, interaction, and loading of active metals on a support.  Additionally, this research evaluated the activity of catalysts and compared them with commercial and catalysts in the absence of additives. The metal oxide nanoparticles were prepared and impregnated on 𝛾-Al2O3 in-situ by using the wetness impregnation method, under conditions 60°C and calcination temperature 520°C. The supported nanocatalyst was calcined to remove the volatile materials and gases. The catalysts were characterized by TPR, BET, BJH, AAS, FT-IR, SEM, and XRD. The prepared nanocatalyst displayed the enhanced catalytic activity for the heavy oil hydrodesulfurization (HDS) containing 21 g/L sulfur. At the acidic pH, the activity of the catalyst was promoted by using EDTA compound as a chelating agent. The sulfur content of the feed was decreased up to 2 g/L at 380°C, 60 bar, and LHSV 1.5h-1 showing an efficient catalyst with the conversion of 90.47%. UR - https://ijcce.ac.ir/article_37259.html L1 - https://ijcce.ac.ir/article_37259_68d13d6d15b2d48c2ef3d3927033c321.pdf ER -