Analysis of phosphate removal from aqueous solutions by hydrocalumite
- Authors
- Son, Jeong-Woo; Kim, Jae-Hyun; Kang, Jin-Kyu; Kim, Song-Bae; Park, Jeong-Ann; Lee, Chang-Gu; Choi, Jae-Woo; Lee, Sang-Hyup
- Issue Date
- 2016
- Publisher
- DESALINATION PUBL
- Keywords
- Hydrocalumite; Hydroxyapatite; Layered double hydroxide; Phosphate removal; Precipitation
- Citation
- DESALINATION AND WATER TREATMENT, v.57, no.45, pp.21476 - 21486
- Indexed
- SCIE
SCOPUS
- Journal Title
- DESALINATION AND WATER TREATMENT
- Volume
- 57
- Number
- 45
- Start Page
- 21476
- End Page
- 21486
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/90180
- DOI
- 10.1080/19443994.2015.1119759
- ISSN
- 1944-3994
- 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).
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