Issue 7, 2019

The preparation of hydroxyapatite from unrefined calcite residues and its application for lead removal from aqueous solutions

Abstract

Calcite originating from waste treatment technologies was utilised for the chemical precipitation of hydroxyapatite (HAP). The physicochemical properties of the as-synthesised-HAP was fully characterised using FT-IR, BET, SEM and TEM, confirming its crystal structure and formation of high purity HAP by XRD. The product was employed for removal of lead from aqueous media at pH 5.0, achieving almost 80% of the adsorption in the first 5 min and a maximum adsorption capacity for Pb2+ of 224.4 mg g−1. A contact time of 40 min was required to achieve equilibrium with Pb2+ uptake of 98%. The kinetics of the cation exchange of HAP from calcite were predicted using integrated rate laws, revealing a pseudo-second order cation exchange process with a rate constant of 6.84 × 10−4 g (mg min)−1. All obtained results are benchmarked against a control HAP sample simultaneously derived from eggshells, which were demonstrated to offer slower kinetics of cation exchange (4.82 × 10−4 g (mg min)−1) and almost half the maximum adsorption capacity (129.1 mg g−1). The results showed that hydroxyapatite synthesised from calcite waste represents a low-cost material for the adsorption of hazardous Pb2+ in contaminated waters and a promising alternative for heavy metals remediation in aquatic environments.

Graphical abstract: The preparation of hydroxyapatite from unrefined calcite residues and its application for lead removal from aqueous solutions

Supplementary files

Article information

Article type
Paper
Submitted
01 Jun 2018
Accepted
23 Jan 2019
First published
30 Jan 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 4054-4062

The preparation of hydroxyapatite from unrefined calcite residues and its application for lead removal from aqueous solutions

E. Bernalte, J. Kamieniak, E. P. Randviir, Á. Bernalte-García and C. E. Banks, RSC Adv., 2019, 9, 4054 DOI: 10.1039/C8RA04701D

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