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May 9, 2026Catalysts3 citationsOpen Access

Simultaneous Adsorptive Removal of Arsenic(V) and Congo Red by a MgZnFe LDH/Triazole Composite with Electrocatalytic Urea Oxidation Application

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SMSamar M. MahgoubAAAbdelghafar M. Abu-ElsaoudSHSeham M. Hamed

Key Points

  • This study aims to develop a novel adsorbent for simultaneously removing arsenic(V) and Congo red from water while allowing for the material's reuse.
  • Synthesis of MgZnFe-LDH/1,2,4-triazole composite via co-precipitation and surface grafting.
  • Batch adsorption experiments assessed the removal efficiency at varying pH and temperature conditions.
  • Characterization techniques included FTIR, XRD, BET, TGA, FESEM, and HRTEM.
  • Maximum Langmuir adsorption capacity reached 204.75 mg g−1 for As(V) and 499.72 mg g−1 for CR at pH 5 and 25 °C.
  • Achieved a UOR peak current density of 184.67 mA cm−2, nearly double that of fresh material, with a charge-transfer resistance of 1.19 Ω.
  • Removal efficiency remained above 85% over three regeneration cycles.

Abstract

Water contamination by arsenic(V) As(V) and Congo red (CR) dye poses concurrent threats to public health and aquatic ecosystems, particularly in regions where metallurgical and textile industries coexist. Developing a single adsorbent capable of simultaneously addressing these chemically distinct pollutants, while recovering value from the spent material remains an open challenge in sustainable water treatment. This study reports the synthesis and evaluation of a novel ternary MgZnFe-LDH/1,2,4-triazole composite (TM-LDH/TZ), engineered for the concurrent adsorptive removal of As(V) and CR, and the subsequent repurposing of the pollutant-loaded material as an electrocatalyst for the urea oxidation reaction (UOR). The composite was prepared via co-precipitation and triazole surface grafting, then characterized by FTIR, XRD, BET, TGA, FESEM, and HRTEM. Batch adsorption experiments examined the influence of pH, adsorbent dose, initial concentration, and temperature, with equilibrium data modeled through Langmuir, Freundlich, Temkin, and the statistically grounded Advanced Monolayer Model (AMM); kinetics were assessed using pseudo-first/second-order and Elovich models. Maximum Langmuir adsorption capacities reached 204.75 mg g−1 for As(V) and 499.72 mg g−1 for CR simultaneously at pH 5 and 25 °C, surpassing the majority of previously reported single-pollutant adsorbents. Elovich and pseudo-second-order kinetics confirmed chemisorption as the governing pathway for As(V) and CR, respectively, while AMM thermodynamic analysis verified spontaneous adsorption across all experimental conditions. The spent composite delivered a UOR peak current density of 184.67 mA cm−2 that is nearly twice that of the fresh material, with a reduced charge-transfer resistance of 1.19 Ω, and removal efficiency remained above 85% through three successive regeneration cycles. The bifunctional design, coupling high-capacity dual-pollutant removal with catalytic valorization of waste, positions TM-LDH/TZ as a circular-economy-aligned platform for advanced water remediation.

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Cite This Study

Mahgoub et al. (2026) studied this question.

synapsesocial.com/papers/69fecfe9b9154b0b82876ed5https://doi.org/10.3390/catal16050434
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