Abstract

Mg–Al layered double hydroxide (Mg–Al LDH) was modified with organic acid anions using a coprecipitation technique, and the uptake of heavy metal ions from aqueous solution by the Mg–Al LDH was studied. Citrate·Mg–Al LDH, malate·Mg–Al LDH, or tartrate·Mg–Al LDH, which had citrate 3− (C 6H 5O 7 3−), malate 2− (C 4H 4O 5 2−), or tartrate 2− (C 4H 4O 6 2−) anions intercalated in the interlayer, was prepared by dropwise addition of a mixed aqueous solution of Mg(NO 3) 2 and Al(NO 3) 3 to a citrate, malate, or tartrate solution at a constant pH of 10.5. These Mg–Al LDHs were found to take up Cu 2+ and Cd 2+ rapidly from an aqueous solution at a constant pH of 5.0. This capacity was mainly attributable to the formation of the citrate–metal, malate–metal, and tartrate–metal complexes in the interlayers of the Mg–Al LDHs. The uptake of Cu 2+ increased in the order malate·Mg–Al LDH < tartrate·Mg–Al LDH < citrate·Mg–Al LDH. The uptake of Cd 2+ increased in the order malate·Mg–Al LDH < tartrate·Mg–Al LDH = citrate·Mg–Al LDH. These differences in Cu 2+ and Cd 2+ uptake were attributable to differences in the stabilities of the citrate–metal, malate–metal, and tartrate–metal complexes. These results indicate that citrate 3−, malate 2−, and tartrate 2− were adequately active as chelating agents in the interlayers of Mg–Al LDHs.

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