TY - JOUR
T1 - Enhanced carbon dioxide mineralization of industrial alkaline wastes through date palm waste-derived activated biochar
AU - El Gamal, Maisa
AU - Mohammad, Ameera F.
AU - Abu-Jdayil, Basim
AU - Hameedi, Suhaib
AU - Ben Salem, Imen
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/11
Y1 - 2025/11
N2 - This study presents a sustainable approach for synthesizing activated biochar (BC) from date palm waste and enhancing its carbon dioxide (CO2) capture capacity through integration with industrial alkaline waste, particularly ladle furnace slag (AW-LF). BC was produced via pyrolysis at 450 °C, 600 °C, and 750 °C and chemically activated using potassium carbonate (K2CO3) and hydrogen peroxide (H2O2). The materials were tested under CO2 gas flow (10 % CO2, 0.6 L/min, 1–2 bar, 22–25 °C) using a fluidized bed reactor. The highest CO2 capture capacity reached 0.94 mmol/g with H2O2-modified BC at a 10 % BC-to-AW-LF ratio. The cumulative CO2 uptake reached a maximum of 13.4 mol/L with K2CO3-activated BC, demonstrating approximately a 380 % increase compared to the performance of unmodified AW-LF slag. Kinetic analysis confirmed the modified Avrami model as the best fit (R2 > 0.99), with the highest rate constant (Kma = 0.0118) observed for H2O2-treated samples. The findings were validated through X-ray Diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Thermogravimetric Analysis (TGA), confirming stable CaCO3 formation and enhanced porosity. Preliminary TGA results suggest up to 8 % weight loss due to CO2 binding, confirming carbonation. The developed adsorbent is cost-effective, scalable, and derived from abundant agricultural and industrial wastes, supporting the circular economy and low-carbon technologies. A preliminary economic assessment estimated the cost of producing 100 g of hydrogen peroxide-modified BC at 6.6 AED (∼1.80 USD), highlighting its feasibility for large-scale applications.
AB - This study presents a sustainable approach for synthesizing activated biochar (BC) from date palm waste and enhancing its carbon dioxide (CO2) capture capacity through integration with industrial alkaline waste, particularly ladle furnace slag (AW-LF). BC was produced via pyrolysis at 450 °C, 600 °C, and 750 °C and chemically activated using potassium carbonate (K2CO3) and hydrogen peroxide (H2O2). The materials were tested under CO2 gas flow (10 % CO2, 0.6 L/min, 1–2 bar, 22–25 °C) using a fluidized bed reactor. The highest CO2 capture capacity reached 0.94 mmol/g with H2O2-modified BC at a 10 % BC-to-AW-LF ratio. The cumulative CO2 uptake reached a maximum of 13.4 mol/L with K2CO3-activated BC, demonstrating approximately a 380 % increase compared to the performance of unmodified AW-LF slag. Kinetic analysis confirmed the modified Avrami model as the best fit (R2 > 0.99), with the highest rate constant (Kma = 0.0118) observed for H2O2-treated samples. The findings were validated through X-ray Diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Thermogravimetric Analysis (TGA), confirming stable CaCO3 formation and enhanced porosity. Preliminary TGA results suggest up to 8 % weight loss due to CO2 binding, confirming carbonation. The developed adsorbent is cost-effective, scalable, and derived from abundant agricultural and industrial wastes, supporting the circular economy and low-carbon technologies. A preliminary economic assessment estimated the cost of producing 100 g of hydrogen peroxide-modified BC at 6.6 AED (∼1.80 USD), highlighting its feasibility for large-scale applications.
KW - Activated biochar
KW - Carbon dioxide capture
KW - Carbonation kinetics
KW - Chemical activation
KW - Date palm waste
KW - Industrial alkaline waste
UR - https://www.scopus.com/pages/publications/105015959640
UR - https://www.scopus.com/pages/publications/105015959640#tab=citedBy
U2 - 10.1016/j.jenvman.2025.127268
DO - 10.1016/j.jenvman.2025.127268
M3 - Article
C2 - 40966874
AN - SCOPUS:105015959640
SN - 0301-4797
VL - 394
JO - Journal of Environmental Management
JF - Journal of Environmental Management
M1 - 127268
ER -