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Amorphous silica alumina supported nickel sulfide catalysts for tunable hydrocracking of crude palm oil to biofuel

  • Hasanudin Hasanudin*
  • , Wiwik Siscia Asany
  • , Akhmad Syoufian
  • , Karna Wijaya
  • , Ahmad Mudzakir
  • , Ahmad Suseno
  • , Nino Rinaldi
  • , Erwan Hermawan
  • , Wan Ryan Asri
  • , Mohammad N. Siddiqui
  • , Tawfik A. Saleh
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

The development of efficient catalysts for hydrocracking of crude palm oil (CPO) remains important for improving the production of renewable hydrocarbon fuels. This study investigates the hydrocracking of CPO over amorphous potassium hydrogen phthalate (KHP)‒templated Si/Al catalysts modified with NiO and NiS, and proposes structure‒activity relationships supported by detailed physicochemical characterization and response surface methodology (RSM). Nickel impregnation and sulfidation form well dispersed NiO and NiS domains without disrupting the mesoporous Si/Al framework. Acidity analysis reveals that all catalysts lacked medium-strength acid sites, and sulfidation generates a surface dominated by weak acid sites while retaining a small fraction of strong acid sites. Catalytic screening indicates that KHP‒Si/Al‒NiS exhibits the highest conversion (78.58 %) and the most favorable biofuel distribution, producing 44.14 % C5‒C9, 30.44 % C10‒C14, and the lowest C22+ fraction (9.26 %), demonstrating the potential of the KHP‒Si/Al‒NiS catalyst as an alternative sulfided catalyst system for hydrocracking by combining the catalytic functionality of NiS with the structural stability of the amorphous mesoporous Si/Al support. RSM‒CCD was then applied to optimize reaction conditions over KHP‒Si/Al‒NiS, revealing temperature and feed flow rate as the dominant variables controlling both conversion and biogasoline fraction. The optimized reaction conditions (677 °C, 11.12 g/min feed flow rate, and 4 g of catalyst) afford 84.30 % conversion and 44.55 % biogasoline fraction. The observed acidity distribution suggests that the predominance of weak acid sites after sulfidation, together with the remaining strong acid sites, contributes to the formation of C5‒C14 hydrocarbons while limiting excessive over-cracking, demonstrating the potential of the catalyst system for tunable biofuel production through process optimization of the hydrocracking operating conditions.

Original languageEnglish
Article number100939
JournalSouth African Journal of Chemical Engineering
Volume57
DOIs
StatePublished - Jul 2026

Bibliographical note

Publisher Copyright:
© 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Amorphous silica-alumina
  • Biofuels
  • Hydrocracking
  • Mesoporous catalyst
  • Nickel sulfide

ASJC Scopus subject areas

  • Catalysis
  • Education
  • Energy (miscellaneous)
  • Process Chemistry and Technology
  • Fluid Flow and Transfer Processes
  • Filtration and Separation

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