Analysis of phosphate removal from aqueous solutions by hydrocalumite

Authors
Son, Jeong-WooKim, Jae-HyunKang, Jin-KyuKim, Song-BaePark, Jeong-AnnLee, Chang-GuChoi, Jae-WooLee, Sang-Hyup
Issue Date
2016-08
Publisher
DESALINATION PUBL
Citation
DESALINATION AND WATER TREATMENT, v.57, no.45, pp.21476 - 21486
Abstract
In this study, phosphate (P) removal from aqueous solutions by hydrocalumite was investigated using batch experiments and model analyses. The maximum phosphate removal capacity was determined to be 127.53mgP/g under the given experimental conditions (hydrocalumite dose=0.05g/L, initial P concentration=2-20mgP/L, reaction time=24h). Model analyses showed that the Elovich model was most suitable for describing the kinetic data, whereas the Redlich-Peterson model provided the best fits to the equilibrium data. Furthermore, phosphate removal by hydrocalumite was not sensitive to pH changes between 4.0 and 11.0. A thermodynamic analysis indicated that phosphate removal by hydrocalumite increased with a rise in temperature from 15 to 45 degrees C, suggesting that the removal process was spontaneous and endothermic (H degrees=32.05kJ/mol, S degrees=112.86J/K/mol, G degrees=-0.47 to -3.86kJ/mol). The phosphate removal capacity in stream water (5.40-17.25mgP/g) was also lower than that in a synthetic P solution (6.86-27.51mgP/g) under the given experimental conditions (initial P concentration=2mgP/L, hydrocalumite dose=0.05-0.3g/L, reaction time=24h). Such a result could possibly be ascribed to the presence of carbonate ions (CO32-) in the stream water, which could interfere with phosphate removal by hydrocalumite through the precipitation of calcium carbonate (CaCO3).
Keywords
LAYERED DOUBLE HYDROXIDES; REGRESSION-ANALYSIS; WASTE-WATER; SORPTION; KINETICS; MG; PHOSPHORUS; EQUILIBRIUM; ADSORPTION; DESORPTION; Hydrocalumite; Hydroxyapatite; Layered double hydroxide; Phosphate removal; Precipitation
ISSN
1944-3994
URI
https://pubs.kist.re.kr/handle/201004/123855
DOI
10.1080/19443994.2015.1119759
Appears in Collections:
KIST Article > 2016
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