TY - JOUR
T1 - Chemically activated biochar layered double hydroxide composites for multifunctional water remediation
T2 - Coupled adsorption, ion exchange, and catalytic degradation mechanisms
AU - El-Sawaf, Ayman K.
AU - Abdelfattah Nassar, Amal
AU - Ebada, A.
AU - Mubarak, Mahmoud F.
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2026/2
Y1 - 2026/2
N2 - A multifunctional Mg–Al–LDH@BC–KOH composite was successfully synthesized via chemical activation of biochar followed by in situ co-precipitation of Mg-Al layered double hydroxide nano sheets for efficient removal of organic and inorganic pollutants from wastewater. The composite had high specific surface area of 712 m2 g−1, pore volume of 0.82 cm3 g−1, and average pore diameter of 4.6 nm, which is a 93.5 % and 78.3 % enhancement in surface area and pore volume compared to BC–KOH (540 m2 g−1, 0.64 cm3 g−1). XRD, FTIR, FESEM, TEM, and XPS characterization confirmed the successful formation of LDH nanosheets (∼25 nm) with uniform deposition onto the biochar surface and strong chemical interaction of Mg2+/Al3+ layers with oxygen containing functional groups of biochar. The composite exhibited higher adsorption capability with maximum adsorption capacities of 243.5 mg g−1 for tetracycline (TC) and 198.7 mg g−1 for arsenate [As(V)], obeying well the Langmuir model (R2 = 0.991 and 0.987) and pseudo-second-order kinetics (R2 > 0.98). The thermodynamic analysis indicated a spontaneous endothermic adsorption process with ΔG° = −9.71 to −11.92 kJ mol−1 and ΔH° = +16.4 kJ mol−1. Under peroxymonosulfate (PMS) activation, Mg–Al–LDH@BC–KOH composite exhibited 94.6 % tetracycline degradation in 25 min with 87 % TOC removal and rate constant (kobs) of 0.157 min−1, which is approximately five times higher than that of pure LDH. Radical scavenging experiments confirmed that SO₄•−, •OH, and 1O₂ species are all involved in the oxidation process, of which MeOH and L histidine inhibited the most (TC removal dropped to 47.2 % and 58.6 %, respectively). The composite was also ideal for recyclability, the adsorption and catalytic efficiency still exceeding 90 % and 87 % after five cycles, and exhibited excellent stability under the existence of coexisting ions and varying pH conditions. The synergistic composite of Mg–Al–LDH nanosheets and KOH activated biochar created a thermally stable (28 % total weight loss), highly reactive hierarchical material that would be capable of integrating ion exchange, catalytic oxidation, and adsorption. The system was operational with minimal energy inputs (0.18 kWh m−3) and acceptable reusability, which suggests its potential use as an ecofriendly high efficiency platform for the removal of antibiotics and heavy metal oxyanions in real wastewater treatment.
AB - A multifunctional Mg–Al–LDH@BC–KOH composite was successfully synthesized via chemical activation of biochar followed by in situ co-precipitation of Mg-Al layered double hydroxide nano sheets for efficient removal of organic and inorganic pollutants from wastewater. The composite had high specific surface area of 712 m2 g−1, pore volume of 0.82 cm3 g−1, and average pore diameter of 4.6 nm, which is a 93.5 % and 78.3 % enhancement in surface area and pore volume compared to BC–KOH (540 m2 g−1, 0.64 cm3 g−1). XRD, FTIR, FESEM, TEM, and XPS characterization confirmed the successful formation of LDH nanosheets (∼25 nm) with uniform deposition onto the biochar surface and strong chemical interaction of Mg2+/Al3+ layers with oxygen containing functional groups of biochar. The composite exhibited higher adsorption capability with maximum adsorption capacities of 243.5 mg g−1 for tetracycline (TC) and 198.7 mg g−1 for arsenate [As(V)], obeying well the Langmuir model (R2 = 0.991 and 0.987) and pseudo-second-order kinetics (R2 > 0.98). The thermodynamic analysis indicated a spontaneous endothermic adsorption process with ΔG° = −9.71 to −11.92 kJ mol−1 and ΔH° = +16.4 kJ mol−1. Under peroxymonosulfate (PMS) activation, Mg–Al–LDH@BC–KOH composite exhibited 94.6 % tetracycline degradation in 25 min with 87 % TOC removal and rate constant (kobs) of 0.157 min−1, which is approximately five times higher than that of pure LDH. Radical scavenging experiments confirmed that SO₄•−, •OH, and 1O₂ species are all involved in the oxidation process, of which MeOH and L histidine inhibited the most (TC removal dropped to 47.2 % and 58.6 %, respectively). The composite was also ideal for recyclability, the adsorption and catalytic efficiency still exceeding 90 % and 87 % after five cycles, and exhibited excellent stability under the existence of coexisting ions and varying pH conditions. The synergistic composite of Mg–Al–LDH nanosheets and KOH activated biochar created a thermally stable (28 % total weight loss), highly reactive hierarchical material that would be capable of integrating ion exchange, catalytic oxidation, and adsorption. The system was operational with minimal energy inputs (0.18 kWh m−3) and acceptable reusability, which suggests its potential use as an ecofriendly high efficiency platform for the removal of antibiotics and heavy metal oxyanions in real wastewater treatment.
KW - Adsorption oxidation synergy
KW - Arsenate removal
KW - Environmental remediation
KW - Layered double hydroxide
KW - Peroxymonosulfate activation
KW - Reactive oxygen species (ROS)
KW - Tetracycline degradation
KW - Wastewater treatment
UR - https://www.scopus.com/pages/publications/105024328538
U2 - 10.1016/j.inoche.2025.115977
DO - 10.1016/j.inoche.2025.115977
M3 - Article
AN - SCOPUS:105024328538
SN - 1387-7003
VL - 184
JO - Inorganic Chemistry Communications
JF - Inorganic Chemistry Communications
M1 - 115977
ER -