Chemically activated biochar layered double hydroxide composites for multifunctional water remediation: Coupled adsorption, ion exchange, and catalytic degradation mechanisms

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Abstract

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.

Original languageEnglish
Article number115977
JournalInorganic Chemistry Communications
Volume184
DOIs
StatePublished - Feb 2026

Keywords

  • Adsorption oxidation synergy
  • Arsenate removal
  • Environmental remediation
  • Layered double hydroxide
  • Peroxymonosulfate activation
  • Reactive oxygen species (ROS)
  • Tetracycline degradation
  • Wastewater treatment

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