Title of article :
Metal speciation measurement by diffusive gradients in thin films technique with different binding phases Original Research Article
Author/Authors :
Weijia Li، نويسنده , , Huijun Zhao، نويسنده , , Peter R. Teasdale، نويسنده , , Richard John، نويسنده , , Feiyue Wang، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
10
From page :
193
To page :
202
Abstract :
Since its invention in the mid-1990s, the diffusive gradients in thin films (DGT) technique has rapidly become one of the most promising in situ sampling techniques for trace metal measurement in natural waters. We investigated here the possibility of using DGT devices with different binding phases to determine different DGT labile fractions of Cd and Cu in laboratory solutions and in natural waters. Several binding phases were studied, including conventional Chelex 100 resin imbedded polyacrylamide hydrogel (Chelex) and several recently developed binding phases, poly(acrylamide-co-acrylic acid) (PAM-PAA) gel, poly(acrylamidoglycolic acid-co-acrylamide) (PAAG-PAM) gel, Whatman P81 cellulose phosphate ion-exchange membrane (P81), and poly(4-styrenesulfonate) (PSS) aqueous solution. Laboratory testing in metal solutions spiked with EDTA or humic acid suggested that all the DGT devices measured only free metal ions and inorganic metal complexes. Upon field testing at both freshwater and seawater sites it was found that the DGT labile metal concentrations measured by different binding phases can be significantly different, suggesting that the DGT labile metal fractions were dependent on binding strength of the binding phase. By designing binding phases that can compete with different natural water complexing ligands to varying extents, it is possible to use these different DGT devices to measure metal speciation in natural waters.
Keywords :
DGT , Complexation , Waters , Metal speciation , In situ analysis
Journal title :
Analytica Chimica Acta
Serial Year :
2005
Journal title :
Analytica Chimica Acta
Record number :
1034609
Link To Document :
بازگشت