<p>The sustainable management and conservation of water treatment residuals (WTRs) are crucial for advancing resource-efficient and environmentally friendly practices. This study investigates the performance of WTRs loaded hydroxyapatite (HAP) in the remediation of aqueous lead (Pb<sup>2+</sup>) and cadmium (Cd<sup>2+</sup>). By integrating HAP into the WTRs, the resultant HAP-WTRs exhibit significantly enhanced capacities for removing Pb<sup>2+</sup> and Cd<sup>2+</sup>, with an optimal HAP to WTRs ratio of 3:2. In monometallic systems, the HAP-WTRs demonstrated adsorption capacities of 84.85&#xa0;mg/g for Pb<sup>2+</sup> and 34.25&#xa0;mg/g for Cd<sup>2+</sup>. However, in bimetallic systems, competitive adsorption was observed, with a higher affinity for Pb<sup>2+</sup> over Cd<sup>2+</sup>. The adsorption kinetics and isotherms align with the pseudo-second-order kinetic model and the Langmuir isotherm model, suggesting that the process is predominantly driven by monolayer chemical adsorption. Microscopic analyses reveal that the adsorption mechanisms of HAP-WTRs involve ion exchange with Al<sup>2+</sup>, Fe<sup>2+</sup>, and Ca<sup>2+</sup>, electrostatic interactions, surface complexation with functional groups such as -OH and -COOH, and co-precipitation with phosphates and carbonates.</p> Graphical Abstract <p></p>

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Recycling Water Treatment Residuals and Hydroxyapatite to Remove Aqueous Lead and Cadmium

  • Meiyang Jiang,
  • Dingwen Zhang,
  • Haonan Cong,
  • Fei Wang,
  • Benyi Cao,
  • Jian Xu

摘要

The sustainable management and conservation of water treatment residuals (WTRs) are crucial for advancing resource-efficient and environmentally friendly practices. This study investigates the performance of WTRs loaded hydroxyapatite (HAP) in the remediation of aqueous lead (Pb2+) and cadmium (Cd2+). By integrating HAP into the WTRs, the resultant HAP-WTRs exhibit significantly enhanced capacities for removing Pb2+ and Cd2+, with an optimal HAP to WTRs ratio of 3:2. In monometallic systems, the HAP-WTRs demonstrated adsorption capacities of 84.85 mg/g for Pb2+ and 34.25 mg/g for Cd2+. However, in bimetallic systems, competitive adsorption was observed, with a higher affinity for Pb2+ over Cd2+. The adsorption kinetics and isotherms align with the pseudo-second-order kinetic model and the Langmuir isotherm model, suggesting that the process is predominantly driven by monolayer chemical adsorption. Microscopic analyses reveal that the adsorption mechanisms of HAP-WTRs involve ion exchange with Al2+, Fe2+, and Ca2+, electrostatic interactions, surface complexation with functional groups such as -OH and -COOH, and co-precipitation with phosphates and carbonates.

Graphical Abstract