Marchat David, Bernache-Assollant Didier, Champion Eric
Faculté des Sciences et Techniques, Science des Procédés Céramiques et de Traitements de Surfaces UMR CNRS 6638, 123 Avenue Albert Thomas, 87060 Limoges Cedex, France.
J Hazard Mater. 2007 Jan 31;139(3):453-60. doi: 10.1016/j.jhazmat.2006.02.040. Epub 2006 Apr 4.
This study deals with the mechanism of the cadmium uptake by synthetic hydroxyapatite (HA: Ca10(PO4)6(OH)2) in aqueous solution. The rate of cadmium fixation by hydroxyapatite was investigated at 10 and 50 degrees C using batch experiments. Inductively coupled plasma atomic emission spectrometry, X-ray diffraction, FT-IR spectroscopy and electron microscopy were used to characterize the starting HA and the samples. The thermal behaviour of the powders was determined with the help of three thermoanalytical techniques (TGA, DTA, and MS) and temperature programmed X-ray diffraction. Cadmium immobilization kinetics can be divided into two steps: substitution of Ca2+ ions by Cd2+ in the HA lattice at the particle's surface, followed by their incorporation into the hydroxyapatite bulk. This results in the formation of an apatite solid solution, which is very important because in this way decontamination and storage can be performed with the same material.
本研究探讨了合成羟基磷灰石(HA:Ca10(PO4)6(OH)2)在水溶液中吸收镉的机制。采用批量实验研究了在10℃和50℃下羟基磷灰石固定镉的速率。使用电感耦合等离子体原子发射光谱法、X射线衍射法、傅里叶变换红外光谱法和电子显微镜对起始HA和样品进行表征。借助三种热分析技术(热重分析、差热分析和质谱)以及程序升温X射线衍射确定了粉末的热行为。镉固定动力学可分为两个步骤:在颗粒表面,HA晶格中的Ca2+离子被Cd2+取代,随后Cd2+离子并入羟基磷灰石本体。这导致形成磷灰石固溶体,这非常重要,因为通过这种方式可以使用相同的材料进行去污和储存。