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New data on arsenic sorption properties of Zn–Al sulphate layered double hydroxides: Influence of competition with other anions
Abstract The adequacy of synthetic Zn–Al-sulphate LDHs to remove arsenic from aqueous systems was tested through sorption experiments, using a series of aqueous solutions with dissolved HAsO4 2− together with other anions (Cl−, SO4 2−, MoO4 2−, HCO3 −, CO3 2−) to assess their competition influence on the As removing process. The competitors were added into the solution both simultaneously and afterwards with respect to HAsO4 2− in order to verify the effectiveness and the possible reversibility of the As sorption process. The results showed that only carbonates species, in particular in the fully deprotonated form CO3 2−, affect significantly the otherwise high efficacy of the sorption process. In fact, up to ~90% of HAsO4 2− can be removed from the solution, decreasing to ~60% in the presence of CO3 2−, whilst up to ~30% of HAsO4 2− can be desorbed when CO3 2− is added afterwards into the solution. Considering the very restricted range of pH where HAsO4 2− and CO3 2− are simultaneously the predominant species in the solution (~10<pH<~11.5), Zn–Al-sulphate LDHs could be successfully used for the treatment of As contaminated waters with pH ranging from circum-neutral to moderately alkaline.
Highlights Zn-Al sulphate LDHs as removers of arsenic from aqueous solution. Up to 90% of initial dissolved arsenic is removed from solution by these LDHs. Competition with other anions may influence arsenic uptake by Zn-Al sulphate LDHs. Anion speciation in solution influences arsenic uptake by Zn-Al sulphate LDHs. Only at pH>10 the As uptake efficiency is significantly affected by carbonate species.
New data on arsenic sorption properties of Zn–Al sulphate layered double hydroxides: Influence of competition with other anions
Abstract The adequacy of synthetic Zn–Al-sulphate LDHs to remove arsenic from aqueous systems was tested through sorption experiments, using a series of aqueous solutions with dissolved HAsO4 2− together with other anions (Cl−, SO4 2−, MoO4 2−, HCO3 −, CO3 2−) to assess their competition influence on the As removing process. The competitors were added into the solution both simultaneously and afterwards with respect to HAsO4 2− in order to verify the effectiveness and the possible reversibility of the As sorption process. The results showed that only carbonates species, in particular in the fully deprotonated form CO3 2−, affect significantly the otherwise high efficacy of the sorption process. In fact, up to ~90% of HAsO4 2− can be removed from the solution, decreasing to ~60% in the presence of CO3 2−, whilst up to ~30% of HAsO4 2− can be desorbed when CO3 2− is added afterwards into the solution. Considering the very restricted range of pH where HAsO4 2− and CO3 2− are simultaneously the predominant species in the solution (~10<pH<~11.5), Zn–Al-sulphate LDHs could be successfully used for the treatment of As contaminated waters with pH ranging from circum-neutral to moderately alkaline.
Highlights Zn-Al sulphate LDHs as removers of arsenic from aqueous solution. Up to 90% of initial dissolved arsenic is removed from solution by these LDHs. Competition with other anions may influence arsenic uptake by Zn-Al sulphate LDHs. Anion speciation in solution influences arsenic uptake by Zn-Al sulphate LDHs. Only at pH>10 the As uptake efficiency is significantly affected by carbonate species.
New data on arsenic sorption properties of Zn–Al sulphate layered double hydroxides: Influence of competition with other anions
Ardau, C. (Autor:in) / Frau, F. (Autor:in) / Lattanzi, P. (Autor:in)
Applied Clay Science ; 80-81 ; 1-9
15.05.2013
9 pages
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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