TY - JOUR
T1 - Enhanced syngas generation from CO2 and CH4
T2 - A sustainable approach using Zr-promoted Ni/POFA-SBA-15 for environmental benefit
AU - Hasnain, Syed Muhammad Wajahat ul
AU - Farooqi, Abid Salam
AU - Ahmed, Usama
AU - Farooqi, Ahmad Salam
AU - Ayodele, Bamidele Victor
AU - Ahmad, Farooq
AU - Abdullah, Bawadi
N1 - Publisher Copyright:
Copyright © 2025. Published by Elsevier B.V.
PY - 2025/12
Y1 - 2025/12
N2 - This study presents a sustainable strategy for enhancing syngas production through the catalytic conversion of CH4 and CO2 using a Zr-promoted Ni-based catalyst supported on SBA-15 synthesized from palm oil fuel ash (POFA), an abundant agro-industrial waste. POFA offers an eco-friendly and cost-effective alternative to conventional silica sources such as tetraethyl orthosilicate. The Ni-Zr/POFA-SBA-15 catalyst was prepared via incipient wetness impregnation method and characterized using XRD, FESEM, and N4 physisorption analyses. Zirconium incorporation improved Ni dispersion and reduced metal particle size, leading to enhanced catalytic activity. A two-step statistical design approach was applied to maximize methane dry reforming (MDR) performance. Initially, a 2-level factorial design was used to identify significant parameters, followed by a rotatable central composite design tool of response surface methodology (RSM) for optimization. The effects of CH4/CO2 ratio (0.5–1.5), reaction temperature (650–850 °C), and time on stream (TOS) (60–240 min) were examined. The screening results demonstrated that all 3 parameters impact MDR performance. The optimum conditions, as determined by RSM, were 811.86 °C, a CH4/CO2 ratio of 1.46, and a 90 min TOS, resulting in 80.41 % CH4 conversion, 97.37 % CO2 conversion, and an H2/CO ratio of 0.95. The experimental validation under these conditions closely matched RSM predictions, with negligible deviation. The catalyst demonstrated excellent thermal stability with only 10.08 % activity loss after 30-h of continuous operation. These findings highlight the potential of POFA-derived SBA-15-supported catalysts as a cost-effective and sustainable option for long-term syngas production.
AB - This study presents a sustainable strategy for enhancing syngas production through the catalytic conversion of CH4 and CO2 using a Zr-promoted Ni-based catalyst supported on SBA-15 synthesized from palm oil fuel ash (POFA), an abundant agro-industrial waste. POFA offers an eco-friendly and cost-effective alternative to conventional silica sources such as tetraethyl orthosilicate. The Ni-Zr/POFA-SBA-15 catalyst was prepared via incipient wetness impregnation method and characterized using XRD, FESEM, and N4 physisorption analyses. Zirconium incorporation improved Ni dispersion and reduced metal particle size, leading to enhanced catalytic activity. A two-step statistical design approach was applied to maximize methane dry reforming (MDR) performance. Initially, a 2-level factorial design was used to identify significant parameters, followed by a rotatable central composite design tool of response surface methodology (RSM) for optimization. The effects of CH4/CO2 ratio (0.5–1.5), reaction temperature (650–850 °C), and time on stream (TOS) (60–240 min) were examined. The screening results demonstrated that all 3 parameters impact MDR performance. The optimum conditions, as determined by RSM, were 811.86 °C, a CH4/CO2 ratio of 1.46, and a 90 min TOS, resulting in 80.41 % CH4 conversion, 97.37 % CO2 conversion, and an H2/CO ratio of 0.95. The experimental validation under these conditions closely matched RSM predictions, with negligible deviation. The catalyst demonstrated excellent thermal stability with only 10.08 % activity loss after 30-h of continuous operation. These findings highlight the potential of POFA-derived SBA-15-supported catalysts as a cost-effective and sustainable option for long-term syngas production.
KW - 2-level factorial design
KW - Heterogeneous catalyst
KW - Optimization
KW - Reforming
KW - Response surface methodology
UR - https://www.scopus.com/pages/publications/105022206642
U2 - 10.1016/j.rineng.2025.107920
DO - 10.1016/j.rineng.2025.107920
M3 - Article
AN - SCOPUS:105022206642
SN - 2590-1230
VL - 28
JO - Results in Engineering
JF - Results in Engineering
M1 - 107920
ER -