AI Article Synopsis

  • The study explored the synthesis of various MgAlFe-layered double hydroxides (LDHs) for removing arsenate and fluoride from water, analyzing factors like pH, dosage, and coexisting ions.
  • Different intercalating anions significantly impacted the adsorption efficiency, and various isotherm equations were used to describe the adsorption data.
  • In competitive systems, fluoride ions were preferentially adsorbed over arsenate, but the MgAlFe-NO-LDH achieved low residual concentrations for both contaminants, complying with global drinking water standards.

Article Abstract

In this study, a series of MgAlFe-LDHs (Cl, NO , intercalation, and calcined products of a CO 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 MgAlFe-CLDH, MgAlFe-Cl-LDH or MgAlFe-NO-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 MgAlFe-Cl-LDH and MgAlFe-NO-LDH. MgAlFe-NO-LDH was used to adsorb arsenate and fluoride in coexisting pollution systems (the concentration of each pollutant was 2 mg L, the adsorbent dosage was 1.5 g L). The remaining arsenic concentration was reduced to less than 10 μg L and the remaining fluoride ion concentration to below 20 μg L 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086567PMC
http://dx.doi.org/10.1039/c8ra05968cDOI Listing

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