Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAIFe-LDHs with different intercalating anions

摘要

In this study, a series of MgAIFe-LDHs (Cl-, NO32-, intercalation, and calcined products of a CO32- interlayer) was synthesized and used for adsorption of arsenate and fluoride in individual contaminants and coexisting pollutant systems. Effects of various factors such as initial pH of solution, dosage of materials, coexisting ions, contact time, and initial pollutant concentrations were evaluated. Experimental results showed that different intercalating anions had a significant effect on adsorption performance of arsenate and fluoride in water. The adsorption of arsenate and fluoride on MgAIFe-CLDH, MgAIFe-Cl-LDH or MgAIFe-NO3-LDH can be described by different adsorption isotherm equations. During the simultaneous removal process, arsenate and fluoride competed for adsorption sites of the adsorbent materials, and the fluoride ions had advantages in the competitive adsorption on MgAIFe-Cl-LDH and MgAIFe-NO3-LDH. MgAIFe-NO3-LDH was used to adsorb arsenate and fluoride in coexisting pollution systems (the concentration of each pollutant was 2 mg L-1, the adsorbent dosage was 1.5 g L-1). The remaining arsenic concentration was reduced to less than 10 mu g L-1 and the remaining fluoride ion concentration to below 20 mu g L-1 which meets the World Health Organization's, EPA's and China's drinking water standards for arsenic and fluoride limits. A possible mechanism is discussed with support from further XRD, SEM, and XPS analysis of the materials after their adsorption.