2016
DOI: 10.1016/j.jece.2015.12.022
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Removal As(V) by sulfated mesoporous Fe–Al bimetallic adsorbent: Adsorption performance and uptake mechanism

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Cited by 14 publications
(7 citation statements)
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“…These results indicated that the ion‐exchange between H 2 AsO 4 − and SO 4 2− was the dominant adsorption mechanism. The result is consistent with other sulphated‐contained arsenate adsorbents . Moreover, it was observed from the regenerated MSZ that the band attributed to As‐O vibration (∼845 cm −1 ) disappeared, and the band ascribed to S‐O (∼1219 cm −1 ) appeared.…”
Section: Resultssupporting
confidence: 89%
“…These results indicated that the ion‐exchange between H 2 AsO 4 − and SO 4 2− was the dominant adsorption mechanism. The result is consistent with other sulphated‐contained arsenate adsorbents . Moreover, it was observed from the regenerated MSZ that the band attributed to As‐O vibration (∼845 cm −1 ) disappeared, and the band ascribed to S‐O (∼1219 cm −1 ) appeared.…”
Section: Resultssupporting
confidence: 89%
“…Further H 2 AsO 4 − species replaced the sulfate groups through the electrostatic attraction mechanism along with the competitive interaction towards OH − groups. 44 The stability of Fe–Al bimetallic particles is found be high in the pH range of 5.0–9.0 signifying the negligible leaching of both Fe and Al species under neutral and weak acidic and alkaline conditions. 45 In the pH range of 4–8, Fe–Cu bimetallic particles exhibited better removal of As( v ) since the pHpzc of Fe–Cu particles is between 8 and 9.…”
Section: Effect Of Solution Ph On Oxidative Sorption Of Arsenitementioning
confidence: 94%
“…92) and is enhanced by sulfate modification. 44 Exchange of sulfate ions with H 2 AsO 4 − is the main sorption mechanism at pH higher than 4, while sorption of H 2 AsO 4 − by protonated hydroxyl groups of Fe and Al and hydrogen bonding of H 3 AsO 4 with unprotonated hydroxyl groups are the arsenate removal mechanisms at pH less than 4. 44…”
Section: Oxidative Sorption By Ironmentioning
confidence: 98%
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