Improved Palm Oil Mill Effluent Degradation by Fe²⁺/Fe³⁺ Ion Exchanger Mediator

Authors

  • Mohd Hafiz Md Ali Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
  • Mohd Afiq Mohd Fauzi Civil Engineering Studies, College of Engineering, Universiti Teknologi MARA, 94300 Kota Samarahan, Sarawak, Malaysia
  • Mohammad Noor Jalil Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia; Electrochemical Material and Sensor (EMaS) Research Group, Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
  • Zainiharyati Mohd Zain Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia; Electrochemical Material and Sensor (EMaS) Research Group, Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
  • Chia Chay Tay Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
  • Hamizah Mohd Zaki Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia

DOI:

https://doi.org/10.24191/jsst.v5i1.90

Keywords:

POME, Fe2 /Fe3 Ion Exchangers, Redox Processes, Degradation

Abstract

This present study investigates the efficiency of using ion exchanger Fe2+/Fe3+ mediator for the degradation of Palm Oil Mill Effluent (POME). The ion exchanger of Fe2+/Fe3+ mediator enhanced the redox reaction in liquid POME degradation. Comprehensive analysis on POME before and after degradation by 0.005 M FeCl3 was conducted by several characterisation techniques, including cyclic voltammetry (CV), Ultraviolet-visible (UV-Vis) spectroscopy, Attenuated Total Reflectance-Fourier Transform Infrared spectroscopy (ATR-FTIR) Analysis, X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET) analysis. The CV analysis provided a better understanding on the oxidation and reduction reaction during the degradation of liquid POME. The identification of chemical bonds and functional groups was carried out by using the ATR-FTIR analysis. The type of crystal or amorphous patterns identified by XRD and surface area measurements were done by using the BET analysis. The findings revealed that the existence of ion exchanger Fe2+/Fe3+ mediator performed redox reaction by CV and the peak current density of oxidation (Ipa) showed similar results for fresh liquid POME and liquid POME+0.005 M FeCl3, that is 1.34 ´ 10-1µA cm-2. Meanwhile, the peak current density of reduction (Ipc) for both samples were -1.33 ´ 10µA cm-2 and -5.89 ´ 101 µA cm-2, respectively. The specific capacitance, C are 125.08 C and 157.71 C for both samples. Spectrometry analysis by UV-Vis spectrometry showed a significant absorbance reduction and chemical shifting when 0.005 M FeCl3 was added to liquid POME. By using the ATR-FTIR analysis, it was revealed that the chemical bonds changed on dried solid POME after degradation with the addition of 0.005 M FeCl3. Amorphous diffractogram patterns were identified for both samples by XRD analysis. An increase in surface area from 0.94 m2 g-1 to 18.55 mg-1 was also revealed from the BET analysis. This research contributes to the knowledge on the role of ion exchangers Fe2+/Fe3+ mediator, providing a foundation for effective liquid POME treatment.

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Published

2025-03-31