Essence of hydroxyapatite in defluoridation of drinking water: A review

Hydroxyapatite (HAp) is the major mineral constituent of vertebrate bones and teeth. It has been well documented that HAp nanoparticles can significantly increase the biocompatibility and bioactivity of man-made biomaterials. Over the past decade, HAp nanoparticles have therefore increasingly been in demand, and extensive efforts have been devoted to develop many synthetic routes, involving both scientifically and economically new features. Several investigations have also been made to determine how critical properties of HAp can be effectively controlled by varying the processing parameters. With such a wide variety of methods for the preparation of HAp nanoparticles, choosing a specific procedure to synthesize a well-defined powder can be laborious; accordingly, in the present review, we have summarized all the available information on the preparation methodologies of HAp, and highlighted the inherent advantages and disadvantages involved in each method. This article is focused on nanosized HAp, although recent articles on microsized particles, especially those assembled from nanoparticles and/or nanocrystals, have also been reviewed for comparison. We have also provided several scientific figures and discussed a number of critical issues and challenges which require further research and development.

A novel magnetic nano-adsorbent (MNP-NH(2)) has been developed by the covalent binding of 1,6-hexadiamine on the surface of Fe(3)O(4) nanoparticles for removal of Cu(2+) ions from aqueous solution. Various factors affecting the uptake behavior such as contact time, temperature, pH, salinity, amount of MNP-NH(2) and initial concentration of Cu(2+) were investigated. The kinetics was evaluated utilizing the Lagergren pseudo-first-order, pseudo-second-order, Elovich and intra-particle diffusion models. The equilibrium data were analyzed using Langmuir, Freundlich, and Dubinin-Radushkevich isotherms. The adsorption was relatively fast and the equilibrium was established within 5 min, and its kinetics followed the pseudo-second-order mechanism, evidencing chemical sorption as the rate-limiting step of sorption mechanism. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities was 25.77 mg g(-1) at pH 6, and 298 K. Thermodynamic parameters showed that the adsorption process was spontaneous, endothermic and chemical in nature. The successive adsorption-desorption studies indicated that the MNP-NH(2) sorbent kept its adsorption and desorption efficiencies constant over 15 cycles. Importantly, MNP-NH(2) was able to remove 98% of Cu(2+) from polluted river and tap water. Copyright © 2010 Elsevier B.V. All rights reserved.