4.7 Article

Effect of pH, ionic strength, and temperature on the phosphate adsorption onto lanthanum-doped activated carbon fiber

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 364, Issue 2, Pages 490-496

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2011.08.067

Keywords

Phosphate removal; Activated carbon fiber; Lanthanum; Adsorption; Kinetics

Funding

  1. Shanghai Promotion Association of Tech-transfer (SPAT) [LM201016, LM201017]
  2. Shanghai Education Development Foundation (SEDF)
  3. Shanghai Promotion of Tech-transfer Foundation (SPTF)
  4. Industry-University-Research Institute of Science and Technology Committee, Baoshan District, Shanghai [CXY-2009-06, CXY-2010-13]
  5. Shanghai Municipal Education Commission [S30109]

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Phosphate removal from polluted water is crucial to preventing eutrophication. Herein, we present the investigation on phosphate adsorption in aqueous solutions by using lanthanum-doped activated carbon fiber (ACF-La). Various batch sorption conditions, e.g., pH, ionic strength, and temperature were tested, and the adsorption mechanisms were discussed. The sorption capacity of ACF-La was higher in acidic solutions than that in basic ones, suggesting that the Lewis acid-base interaction gradually dominated the adsorption process with the increase in pH values. The degree of phosphate removal decreased with the enhancement of the ionic strength of the solution, meaning that the adsorption of phosphate on ACF-La was strongly dependent on ionic strength. Employing the pseudo first- and second-order, and intra-particle diffusion models to evaluate the adsorption kinetics of phosphate onto ACF-La indicated that the second-order model best fits the experimental data. The presence of chloride ion in solutions increased the effect of intra-particle diffusion on the adsorption of phosphate onto ACF-La but reduced the overall rate of the adsorption. The thermodynamic parameters were determined which revealed the feasibility, spontaneity, and endothermic nature of adsorption. (C) 2011 Elsevier Inc. All rights reserved.

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