Complexation of Cobalt by Natural Ligands in Freshwater
Ligand exchange with dimethylglyoxime (DMG) and dif ferential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic concentrations [Co2+] and Co(II) complexation by natural organic ligands in freshwater. [Co2+] and the complexing parameters were calculated on the ba...
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Published in | Environmental science & technology Vol. 32; no. 14; pp. 2043 - 2050 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Chemical Society
15.07.1998
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Abstract | Ligand exchange with dimethylglyoxime (DMG) and dif ferential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic concentrations [Co2+] and Co(II) complexation by natural organic ligands in freshwater. [Co2+] and the complexing parameters were calculated on the basis of the thermodynamic equilibria between added and natural ligands. The optimal working conditions were carefully evaluated in synthetic solutions and in natural freshwater samples. The results from samples collected at various sites from the Aare and Rhine Rivers and the Biel and Lucerne Lakes, Switzerland, are presented. The total dissolved Co concentrations are in the range of 0.5−6.5 nM, and [Co2+] is in the range of 0.05−0.5 nM. Organic complexes of Co are predominant in most samples with 80−96% of total dissolved Co. A one-ligand model could well fit the titrations of freshwater samples with Co(II) (using the FITEQL program). The conditional stability constants of the natural ligands were computed to be log K = 9.5−11.6 (pH 8.0 ± 0.1), and the ligand concentrations were [L] = 1.4−7.6 nM. The reliability and applicability of the technique and the implications of the results are discussed. |
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AbstractList | ACo2+B and Co(II) complexation determined by ligand exchange and DPCSV show 80-96% in the form of natural organic complexes in Swiss rivers and lakes. Ligand exchange with dimethylglyoxime (DMG) and dif ferential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic concentrations [Co2+] and Co(II) complexation by natural organic ligands in freshwater. [Co2+] and the complexing parameters were calculated on the basis of the thermodynamic equilibria between added and natural ligands. The optimal working conditions were carefully evaluated in synthetic solutions and in natural freshwater samples. The results from samples collected at various sites from the Aare and Rhine Rivers and the Biel and Lucerne Lakes, Switzerland, are presented. The total dissolved Co concentrations are in the range of 0.5−6.5 nM, and [Co2+] is in the range of 0.05−0.5 nM. Organic complexes of Co are predominant in most samples with 80−96% of total dissolved Co. A one-ligand model could well fit the titrations of freshwater samples with Co(II) (using the FITEQL program). The conditional stability constants of the natural ligands were computed to be log K = 9.5−11.6 (pH 8.0 ± 0.1), and the ligand concentrations were [L] = 1.4−7.6 nM. The reliability and applicability of the technique and the implications of the results are discussed. Ligand exchange with dimethylglyoxime (DMG) and differential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic concentrations [Co super(2+)] and Co(II) complexation by natural organic ligands in freshwater. [Co super(2+)] and the complexing parameters were calculated on the basis of the thermodynamic equilibria between added and natural ligands. The optimal working conditions were carefully evaluated in synthetic solutions and in natural freshwater samples. The results from samples collected at various sites from the Aare and Rhine Rivers and the Biel and Lucerne Lakes, Switzerland, are presented. The total dissolved Co concentrations are in the range of 0.5-6.5 nM, and [Co super(2+)] is in the range of 0.05-0.5 nM. Organic complexes of Co are predominant in most samples with 80-96% of total dissolved Co. A one-ligand model could well fit the titrations of freshwater samples with Co(II) (using the FITEQL program). The conditional stability constants of the natural ligands were computed to be log K = 9.5-11.6 (pH 8.0 plus or minus 0.1), and the ligand concentrations were [L] = 1.4-7.6 nM. The reliability and applicability of the technique and the implications of the results are discussed. |
Author | Albrecht, Achim Qian, Jin Sigg, Laura Xue, Han Bin |
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Keywords | Freshwater environment Complexation Nuclear industry Radioactive pollution Ligand Surface water Water pollution Natural compound Radioisotope Cobalt Organic compounds |
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Snippet | Ligand exchange with dimethylglyoxime (DMG) and dif ferential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic... ACo2+B and Co(II) complexation determined by ligand exchange and DPCSV show 80-96% in the form of natural organic complexes in Swiss rivers and lakes. Ligand exchange with dimethylglyoxime (DMG) and differential pulse cathodic stripping voltammetry (DPCSV) was applied to determine free Co(II) ionic... |
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SubjectTerms | Animal, plant and microbial ecology Applied ecology Applied sciences Biological and medical sciences Biological and physicochemical phenomena Chemical bonds Chemistry Cobalt Earth sciences Earth, ocean, space Ecotoxicology, biological effects of pollution Engineering and environment geology. Geothermics Exact sciences and technology Fresh water environment Fundamental and applied biological sciences. Psychology Natural water pollution Pollution Pollution, environment geology Thermodynamics Water Water treatment and pollution |
Title | Complexation of Cobalt by Natural Ligands in Freshwater |
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