Adsorptive removal of fluoride from water using nanoscale aluminium oxide hydroxide (AlOOH)

TLDR: In this article, a series of batch adsorption experiments were carried out to assess parameters that influence the fluoride removal process, such as contact time and adsorbent dose, initial fluoride concentration, and pH.

Abstract: In this study the fluoride removal potential of nanoscale aluminium oxide hydroxide (nano-AlOOH) has been investigated. The material was produced using aluminium nitrate (Al(NO 3 ) 3 . 9H 2 O, 95%), and ammonium bicarbonate (NH 4 HCO 3 , 98%) and its density and mineralogy were investigated. A series of batch adsorption experiments were carried out to assess parameters that influence the adsorption process. The parameters considered were contact time and adsorbent dose, initial fluoride concentration, and pH. Results showed that most of the adsorption took place during the first 30 min; and equilibrium was reached at one hour contact time with an optimum adsorbent dose of 1.6 g L -1 for initial fluorideconcentration of 20 mg L -1 . The removal efficiency of fluorideincreased with increase in adsorbent dosage. The fluoride removal efficiency was increased as the pH of the solution increases from pH 3 to 8, but any further increase in pH led to a decrease in fluoride removal efficiency. Maximum adsorption occurred at around pH 7 with initial fluoride concentration of 20 mg L -1 . The adsorption data were well fitted to the Langmuir isotherm model with a maximum adsorption capacity of 62.5 mg F - g -1 . The kinetic studies showed that the adsorption of fluoride by nano-AlOOH obeys a pseudo-second order rate equation. The intraparticle diffusion was not a rate-controlling step for the adsorption process. Thus, the overall study indicates that nano-AlOOH is an efficient defluoridating material. KEY WORDS : Nanoscale AlOOH, Defluoridation, Fluoride removal efficiency, Adsorption capacity, Adsorption kinetics, Adsorption mechanism Bull. Chem. Soc. Ethiop. 2014 , 28(2), 215-227. DOI: http://dx.doi.org/10.4314/bcse.v28i2.6