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Removal of lead ions in aqueous solution by hydroxyapatite/polyurethane composite foams

Authors
Jang, Suk HyunMin, Byung GilJeong, Young GyuLyoo, Won SeokLee, Sang Cheol
Issue Date
15-Apr-2008
Publisher
ELSEVIER SCIENCE BV
Keywords
adsorbent; composite foam; heavy metals; hydroxyapatite; polyurethane
Citation
JOURNAL OF HAZARDOUS MATERIALS, v.152, no.3, pp.1285 - 1292
Journal Title
JOURNAL OF HAZARDOUS MATERIALS
Volume
152
Number
3
Start Page
1285
End Page
1292
URI
https://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/19244
DOI
10.1016/j.jhazmat.2007.08.003
ISSN
0304-3894
Abstract
We have prepared hydroxyapatite/polyurehthane (HAp/PU) composite foams with two different HAp contents of 20 and 50 wt.% and investigated their removal capability of Pb2+ ions from aqueous solutions with various initial Pb2+ ion concentrations and pH values of 2-6. HAp/PU composite foams synthesized exhibited well-developed open pore structures which provide paths for the aqueous solution and adsorption sites for Pb2+ ions. With increasing the HAp content in the composites, the removal capability of Pb2+ ions by the composite foams increases owing to the higher adsorption capacity, whereas the removal rate is slower due to the less uniform dispersity of HAp in composite foams. The removal rate of Pb2+ ions is also slower with increasing the initial Pb2+ ion concentration in aqueous solutions. The removal mechanism of Pb2+ ion by the composites is varied, depending on the pH value of aqueous solution: the dissolution of HAp and precipitation of hydroypyromorphite is dominant at lower pH 2-3, the adsorption of Pb2+ ions on the HAp/PU composite surface and ion exchange reaction between Ca2+ of HAp and Pb2+ in aqueous solution is dominant at higher pH 5-6, and two removal mechanisms compete at pH 4. The equilibrium removal process of Pb2+ ions by the HAp/PU composite foam at pH 5 was described well with the Langmuir isotherm model, resulting in the maximum adsorption capacity of 150 mg/g for the composite foam with 50 wt.% HAp content. (c) 2007 Elsevier B.V. All rights reserved.
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