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Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions
In this study, a series of MgAlFe-LDHs (Cl(−), NO(3)(−), intercalation, and calcined products of a CO(3)(2−) 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 solu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086567/ https://www.ncbi.nlm.nih.gov/pubmed/35548142 http://dx.doi.org/10.1039/c8ra05968c |
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author | Hongtao, Lu Shuxia, Liu Hua, Zhang Yanling, Qiu Daqiang, Yin Jianfu, Zhao Zhiliang, Zhu |
author_facet | Hongtao, Lu Shuxia, Liu Hua, Zhang Yanling, Qiu Daqiang, Yin Jianfu, Zhao Zhiliang, Zhu |
author_sort | Hongtao, Lu |
collection | PubMed |
description | In this study, a series of MgAlFe-LDHs (Cl(−), NO(3)(−), intercalation, and calcined products of a CO(3)(2−) 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(3)-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(3)-LDH. MgAlFe–NO(3)-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 μg L(−1) and the remaining fluoride ion concentration to below 20 μg 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. |
format | Online Article Text |
id | pubmed-9086567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90865672022-05-10 Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions Hongtao, Lu Shuxia, Liu Hua, Zhang Yanling, Qiu Daqiang, Yin Jianfu, Zhao Zhiliang, Zhu RSC Adv Chemistry In this study, a series of MgAlFe-LDHs (Cl(−), NO(3)(−), intercalation, and calcined products of a CO(3)(2−) 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(3)-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(3)-LDH. MgAlFe–NO(3)-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 μg L(−1) and the remaining fluoride ion concentration to below 20 μg 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. The Royal Society of Chemistry 2018-09-27 /pmc/articles/PMC9086567/ /pubmed/35548142 http://dx.doi.org/10.1039/c8ra05968c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Hongtao, Lu Shuxia, Liu Hua, Zhang Yanling, Qiu Daqiang, Yin Jianfu, Zhao Zhiliang, Zhu Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title | Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title_full | Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title_fullStr | Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title_full_unstemmed | Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title_short | Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions |
title_sort | comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto mgalfe-ldhs with different intercalating anions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086567/ https://www.ncbi.nlm.nih.gov/pubmed/35548142 http://dx.doi.org/10.1039/c8ra05968c |
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