Copper Speciation in Glacial Stream Waters of Rutor Glacier (Aosta Valley, Italy)

2004 ◽  
Vol 57 (10) ◽  
pp. 945 ◽  
Author(s):  
Damiano Monticelli ◽  
Constant M. G. van den Berg ◽  
Andrea Pozzi ◽  
Carlo Dossi

The chemical speciation of copper in stream waters from Rutor Glacier was determined by cathodic stripping voltammetry with ligand competition against salicylaldoxime. The complexation of salicylaldoxime was calibrated at various calcium concentrations, the major competing cation in these waters. Copper concentrations (3–7 nM) were approximately ten-fold lower than typical for rain waters in this region, indicating that copper had been removed by adsorption onto rock and other particles. Strong copper binding ligands, with log K′CuL = 12.5–12.9, were detected in all samples, including waters emerging from beneath the glacier, with no detectable change in the ligand composition down stream. The results suggest that the ligands could originate from in situ production from algae in snow and ice, or directly from the precipitation.

2015 ◽  
Vol 49 (6) ◽  
pp. 613-620 ◽  
Author(s):  
Masahiro Yamamoto ◽  
Hitoshi Kodamatani ◽  
Yuriko Kono ◽  
Akinori Takeuchi ◽  
Ken Takai ◽  
...  

2009 ◽  
Vol 74 (4) ◽  
pp. 599-610 ◽  
Author(s):  
Mohammad Bagher Gholivand ◽  
Alireza Pourhossein ◽  
Mohsen Shahlaei

A sensitive and selective procedure is presented for the voltammetric determination of lead. The procedure involves an adsorptive accumulation of lead L-3-(3,4-dihydroxyphenyl)alanine (LDOPA) on a hanging mercury drop electrode, followed by a stripping voltammetric measurement of reduction current of an adsorbed complex at –0.15 V (vs Ag|AgCl). Optimum conditions for lead analysis include pH 8.5, 80 μM LDOPA and accumulation potential –0.15 V (vs Ag|AgCl). The peak currents are proportional to the lead concentration 1–300 nmol l–1 with a detection limit of 0.6 nmol l–1 and accumulation time 60 s. The method was used for the determination of lead in blood, dry tea and also in waters.


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