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Conversion of Isopropanol to Diisopropyl Ether over Cobalt Phosphate Modified Natural Zeolite Catalyst Hasanudin, Hasanudin; Asri, Wan Ryan; Rahmawati, Rahmawati; Riyanti, Fahma; Maryana, Roni; Al Muttaqii, Muhammad; Rinaldi, Nino; Hadiah, Fitri; Novia, Novia
Bulletin of Chemical Reaction Engineering & Catalysis 2024: BCREC Volume 19 Issue 2 Year 2024 (August 2024)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20144

Abstract

This study aims to produce diisopropyl ether (DIPE) via isopropanol dehydration using cobalt-phosphate-supported natural zeolite catalysts. The catalytic activities of the zeolite/CoO and zeolite/Co(H2PO4)2 were compared. The as-prepared catalysts were assessed using X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared (FTIR) spectroscopy, and N2 adsorption-desorption. Surface acidity was determined using the gravimetric method with pyridine as the probe. The results of this study showed that natural zeolite was favorably impregnated by CoO and Co(H2PO4)2 species. The impregnation process affected the textural and acidic features of the catalysts. The zeolite/Co(H2PO4)2 catalyst with a loading of 8 mEq.g-1 exhibited the highest surface acidity of 1.827 mmol.g-1. This catalyst also promoted the highest catalytic activity towards isopropanol dehydration, with an isopropanol conversion of 66.19%, DIPE selectivity, and yield of 46.72% and 34.99%, respectively. The cobalt phosphate species promoted higher catalytic activity for isopropanol dehydration than the CoO species. This study demonstrated the potential of cobalt phosphate-supported natural zeolite catalysts for DIPE production with adequate performance. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
Pyrolysis of Puspa Wood Sawdust and Sugarcane Bagasse into Biochar Asri, Wan Ryan; Mara, Ady; Desnelli, Desnelli; Hasanudin*, Hasanudin
Aceh International Journal of Science and Technology Vol 11, No 1 (2022): April 2022
Publisher : Graduate School of Syiah Kuala University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13170/aijst.11.1.25066

Abstract

Puspa wood sawdust and sugarcane bagasse are abundantly available but have low carbon content and nutrients. The carbon content and nutrients could be increased by converting biomass into biochar through pyrolysis. The independent variables of pyrolysis were essential to investigate because those inherently influence biochar quality. In this study, the effect of pyrolysis temperature (300, 350, 400, 450, and 500 C) and time (30, 60, 90 mins) on the biochar characteristic such as pH, yield, and proximate compositions were determined. The total nitrogen, P2O5, and K2O content at optimum condition biochar were also investigated. The data analysis showed that the pyrolysis temperature and time increment positively correlated to the pH, ash content, and carbon content. At the same time, the yield and volatile matter were vice versa. Both biochar's optimum pyrolysis temperature and time were achieved at 500 and 90 minutes. The carbon content and nutrient of biochar were also increased compared to the biomass. The pyrolysis method has enhanced biomass quality, and the biochar may be used as a growing media and soil amendment. It can be concluded that the sugarcane bagasse biochar was more likely favorable than puspa wood sawdust biochar due to its higher fixed carbon and nutrient content
Effect of Aluminium Loading on SiO2/Al2O3-NiMo Catalysts Synthesized via KHP-template for Crude Palm Oil Hydrocracking Hasanudin, Hasanudin; Nakashima, Mhika; Asri, Wan Ryan; Novia, Novia; Hadiah, Fitri; Maryana, Roni; Al Muttaqii, Muhammad; Rinaldi, Nino
Bulletin of Chemical Reaction Engineering & Catalysis 2025: BCREC Volume 20 Issue 4 Year 2025 (December 2025) (In Progress Issue)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20483

Abstract

The present study evaluates the catalytic activity of SiO2/Al2O3‒x and SiO2/Al2O3‒x‒NiMo (where x = 5, 10, 25 g of aluminium weight) synthesized using a potassium hydrogen phthalate (KHP) template-assisted route for the hydrocracking of crude palm oil (CPO) into biofuels. Increasing Al weight modified acidity, porosity, and NiMo dispersion, leading to distinct catalytic behavior. The optimal SiO2/Al2O3‒x‒NiMo catalyst (10 g Al) achieved ~94% conversion, dominated by jet fuel-range hydrocarbons (C10-C14) through synergistic hydrodeoxygenation and acid-catalyzed cracking-isomerization pathway. The enhanced performance originates from the balance between acidity and metal dispersion, highlighting that both template selection and Al loading govern the design of efficient SiO2/Al2O3‒NiMo catalysts for biofuel production. Copyright © 2025 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).