TY - JOUR
T1 - Preparation of Cu-Al layered double hydroxide intercalated with ethylenediaminetetraacetate by coprecipitation and its uptake of rare earth ions from aqueous solution
AU - Kameda, Tomohito
AU - Hoshi, Kazuaki
AU - Yoshioka, Toshiaki
N1 - Funding Information:
This research was partially supported by the Ministry of Education, Science, Sports, and Culture , Grand-in-Aid for Young Scientists (A), 21681007 , 2009-2012.
PY - 2013
Y1 - 2013
N2 - A Cu-Al layered double hydroxide intercalated with ethylenediaminetetraacetate (edta•Cu-Al LDH) was prepared by the dropwise addition of a Cu-Al nitrate solution to an edta solution at constant pH values of 8.0, 9.0, and 10.0. The edta•Cu-Al LDH had Hedta3- in the interlayer. Furthermore, the preparation at pH 8.0 resulted in the intercalation of Cu(edta)2-. The edta•Cu-Al LDH was found to take up rare earth ions from aqueous solution. The uptake of Sc3+ and Y 3+ by edta•Cu-Al LDH was attributed to both the chelating functions of the edta ion in the interlayer and the chemical properties of Cu-Al LDH itself. The uptake of La3+ by edta•Cu-Al LDH was primarily caused by the chelating function of edta ions in the interlayer. The edta ions in the edta•Cu-Al LDH interlayer formed chelate complexes in the order Sc3+ > Y3+ > La3+ due to their relative stabilities, Sc(edta)- > Y(edta)- > La(edta) -. Thus, edta ions retain their chelating function even when intercalated in a Cu-Al LDH interlayer.
AB - A Cu-Al layered double hydroxide intercalated with ethylenediaminetetraacetate (edta•Cu-Al LDH) was prepared by the dropwise addition of a Cu-Al nitrate solution to an edta solution at constant pH values of 8.0, 9.0, and 10.0. The edta•Cu-Al LDH had Hedta3- in the interlayer. Furthermore, the preparation at pH 8.0 resulted in the intercalation of Cu(edta)2-. The edta•Cu-Al LDH was found to take up rare earth ions from aqueous solution. The uptake of Sc3+ and Y 3+ by edta•Cu-Al LDH was attributed to both the chelating functions of the edta ion in the interlayer and the chemical properties of Cu-Al LDH itself. The uptake of La3+ by edta•Cu-Al LDH was primarily caused by the chelating function of edta ions in the interlayer. The edta ions in the edta•Cu-Al LDH interlayer formed chelate complexes in the order Sc3+ > Y3+ > La3+ due to their relative stabilities, Sc(edta)- > Y(edta)- > La(edta) -. Thus, edta ions retain their chelating function even when intercalated in a Cu-Al LDH interlayer.
KW - Coprecipitation
KW - Cu-Al layered double hydroxide
KW - Ethylenediaminetetraacetate
KW - Rare earth
KW - Uptake
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U2 - 10.1016/j.solidstatesciences.2012.12.010
DO - 10.1016/j.solidstatesciences.2012.12.010
M3 - Article
AN - SCOPUS:84872721497
SN - 1293-2558
VL - 17
SP - 28
EP - 34
JO - Solid State Sciences
JF - Solid State Sciences
ER -