Published January 1, 2022 | Version v1
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Interactions of Ni/ZnO with alumina support and their influence on deep reactive adsorption desulfurization

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Double hydrolysis mesoporous alumina (DHA) synthesized via hydrothermal technique and used as support for the loading of ZnO and Ni. The desulfurization activities and their interactions of Ni/ZnO/DHA adsorbents were compared with Ni/ZnO supported on commercially prepared alumina (Com). The higher breakthrough desulfurization activity and sulfur adsorption capability of these catalysts are influenced by the binding extant of Zn/Ni atoms with Al2O3 support, more free ZnO/Ni species and the formation of inactive ZnAl2O4 phases. The catalysts were characterized using nuclear magnetic resonance (NMR) spectroscopy, UV-vis diffuse reflectance spectroscopy (UV-vis DRS), Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Raman spectroscopy, H-2-temperature programmed reduction (H-2-TPR) and N-2 adsorption-desorption. Desulfurization activity shows that Ni/ZnO/DHA-80 degrees C catalyst achieved an excellent breakthrough sulfur removal (10 mg/L) up to 30.26 mL responsible for 110.4 mg S/g sulphur adsorption capability. This desulfurization performance is one fourth fold higher as compared to commercial Ni/ZnO/Com catalyst, achieving a compromised desulfurization activity of 1300 mg/L at set 30.26 mL model fuel flow with 38 mg S/g accumulative sulfur capacity. Detailed characterization results show that, the superior desulfurization activity shown by Ni/ZnO/DHA catalyst is due to the presence of meagre amount of unsaturated pentacoordinate Al3+ centers on Ni/ZnO/DHA surface which are responsible for lesser interaction of Ni/ZnO with Al2O4 and reduce the formation of inactive spinal ZnAl2O4 and NiAl2O4 phase even after many regeneration cycles which increases the active ZnO molar concentration as compared to Ni/ZnO/Com catalyst. (C) 2022 Elsevier B.V. All rights reserved.

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