<p>This study investigates the catalytic specificity of sulfonated palm kernel shell (PKS)-derived biochar for the esterification of free fatty acids (FFA) in high-acid crude palm oil (HACPO). Biochar was prepared by pyrolysis (500&#xa0;°C, 5&#xa0;h, N<sub>2</sub>), activated with KOH (2&#xa0;M, 1:4 w/v, 90&#xa0;°C, 5&#xa0;h) and HCl (1&#xa0;M, 1:4 w/v), and sulfonated with concentrated H<sub>2</sub>SO<sub>4</sub> (1:4 mass ratio, 100&#xa0;°C, 5&#xa0;h). Comprehensive characterization using FTIR, XPS, XRD, and N<sub>2</sub> physisorption revealed that KOH activation generated substantial microporosity (BET surface area 251.85&#xa0;m<sup>2</sup>/g), which was subsequently blocked by the grafted –SO<sub>3</sub>H groups after sulfonation, causing the surface area to collapse to 4.95&#xa0;m<sup>2</sup>/g. XPS confirmed the exclusive presence of covalently bound aromatic –SO<sub>3</sub>H groups (S 2p at 168.7&#xa0;eV) with no residual sulfate impurities. The resulting catalyst exhibited a competitive acid site density of 2.80&#xa0;mmol&#xa0;g⁻<sup>1</sup> and achieved an 84.44% FFA conversion at a 4 wt % catalyst loading. Notably, the near-complete loss of internal porosity confined the active acid sites predominantly to the external particle surface, creating a catalyst that is highly specific toward FFA esterification while showing negligible activity for triglyceride transesterification. This pore-blocking-driven substrate selectivity establishes a clear structure–activity relationship and highlights the potential of PKS-derived sulfonated biochar as a selective solid-acid catalyst for high-FFA feedstock pretreatment.</p>

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Sulfonated palm kernel shell biochar as a pore-blocking-driven selective solid acid catalyst for free fatty acid esterification in high-acid crude palm oil

  • Ahmad Nasir Pulungan,
  • Junifa Layla Sihombing,
  • Agus Kembaren,
  • Dian Wardana,
  • Annisya Dwi Putri Zulmi,
  • Dika Fahreza,
  • Immanuel Veron Silitonga,
  • Rahayu Rahayu

摘要

This study investigates the catalytic specificity of sulfonated palm kernel shell (PKS)-derived biochar for the esterification of free fatty acids (FFA) in high-acid crude palm oil (HACPO). Biochar was prepared by pyrolysis (500 °C, 5 h, N2), activated with KOH (2 M, 1:4 w/v, 90 °C, 5 h) and HCl (1 M, 1:4 w/v), and sulfonated with concentrated H2SO4 (1:4 mass ratio, 100 °C, 5 h). Comprehensive characterization using FTIR, XPS, XRD, and N2 physisorption revealed that KOH activation generated substantial microporosity (BET surface area 251.85 m2/g), which was subsequently blocked by the grafted –SO3H groups after sulfonation, causing the surface area to collapse to 4.95 m2/g. XPS confirmed the exclusive presence of covalently bound aromatic –SO3H groups (S 2p at 168.7 eV) with no residual sulfate impurities. The resulting catalyst exhibited a competitive acid site density of 2.80 mmol g⁻1 and achieved an 84.44% FFA conversion at a 4 wt % catalyst loading. Notably, the near-complete loss of internal porosity confined the active acid sites predominantly to the external particle surface, creating a catalyst that is highly specific toward FFA esterification while showing negligible activity for triglyceride transesterification. This pore-blocking-driven substrate selectivity establishes a clear structure–activity relationship and highlights the potential of PKS-derived sulfonated biochar as a selective solid-acid catalyst for high-FFA feedstock pretreatment.