Adsorptive cathodic stripping voltammetric determination of gold (III) in the presence of yeast mannan
- Lack, Barbara, Duncan, John R, Nyokong, Tebello
- Authors: Lack, Barbara , Duncan, John R , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293151 , vital:57060 , xlink:href="https://doi.org/10.1016/S0003-2670(98)00736-3"
- Description: Adsorptive cathodic stripping voltammetric (AdCSV) studies of gold(III) on a glassy carbon electrode and in the presence of yeast mannan are reported. These studies give evidence of the formation of a complex between gold(III) and mannan in acid media as judged by the enhancement in the AdCSV currents and shift in the reduction peak of gold(III) in the presence of mannan. The AdCSV currents were linearly dependent on gold(III) concentrations ranging from 7.0 × 10−7 to 3.0 × 10−4 mol dm−3. A detection limit of 6.0 × 10−8 mol dm−3 was obtained. Interferences of copper(II) were observed in the presence of mannan, but there was no significant interference of silver(I).
- Full Text:
- Authors: Lack, Barbara , Duncan, John R , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293151 , vital:57060 , xlink:href="https://doi.org/10.1016/S0003-2670(98)00736-3"
- Description: Adsorptive cathodic stripping voltammetric (AdCSV) studies of gold(III) on a glassy carbon electrode and in the presence of yeast mannan are reported. These studies give evidence of the formation of a complex between gold(III) and mannan in acid media as judged by the enhancement in the AdCSV currents and shift in the reduction peak of gold(III) in the presence of mannan. The AdCSV currents were linearly dependent on gold(III) concentrations ranging from 7.0 × 10−7 to 3.0 × 10−4 mol dm−3. A detection limit of 6.0 × 10−8 mol dm−3 was obtained. Interferences of copper(II) were observed in the presence of mannan, but there was no significant interference of silver(I).
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Cobalt (II) porphyrazine catalysed reduction of nitrite
- Thamae, Mamothibe, Nyokong, Tebello
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293162 , vital:57061 , xlink:href="https://doi.org/10.1016/S0022-0728(99)00224-7"
- Description: Studies on the catalytic reduction of nitrite on carbon electrodes modified with Co(II) tetra-2,3-pyridinoporphyrazine (CoTppa, 1), N,N′,N′′,N′′′-tetramethyltetra-2,3-pyridinoporphyrazine ([CoTm-2,3-tppa]4+, 2) and Co(II) N,N′,N′′,N′′′-tetramethyltetra-3,4-pyridinoporphyrazine ([CoTm-3,4-tppa]4+, 3) are reported. There is a close correspondence between the proximity of the methyl groups to the porphyrazine ring and the catalytic activity of the porphyrazine complexes. Bulk electrolysis gave ammonia and hydroxylamine as some of the products. The catalytic activity of the cationic complex, 3, towards the detection of low concentrations of nitrite (less than 10−9 M) in water containing sodium sulfate, was compared with the activities of the anionic cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−, 4) and the mixed [CoIITm-3,4-tppa]4+·[CoTSPc]4− (5) complexes. Complex 5 showed the best catalytic activity of the three in that large currents were obtained for very low concentrations of nitrite.
- Full Text:
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293162 , vital:57061 , xlink:href="https://doi.org/10.1016/S0022-0728(99)00224-7"
- Description: Studies on the catalytic reduction of nitrite on carbon electrodes modified with Co(II) tetra-2,3-pyridinoporphyrazine (CoTppa, 1), N,N′,N′′,N′′′-tetramethyltetra-2,3-pyridinoporphyrazine ([CoTm-2,3-tppa]4+, 2) and Co(II) N,N′,N′′,N′′′-tetramethyltetra-3,4-pyridinoporphyrazine ([CoTm-3,4-tppa]4+, 3) are reported. There is a close correspondence between the proximity of the methyl groups to the porphyrazine ring and the catalytic activity of the porphyrazine complexes. Bulk electrolysis gave ammonia and hydroxylamine as some of the products. The catalytic activity of the cationic complex, 3, towards the detection of low concentrations of nitrite (less than 10−9 M) in water containing sodium sulfate, was compared with the activities of the anionic cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−, 4) and the mixed [CoIITm-3,4-tppa]4+·[CoTSPc]4− (5) complexes. Complex 5 showed the best catalytic activity of the three in that large currents were obtained for very low concentrations of nitrite.
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Interactions of cobalt (II) tetrasulfophthalocyanine with nitrite in the presence of nitrate and perchlorate ions
- Chebotareva, Natalia, Nyokong, Tebello
- Authors: Chebotareva, Natalia , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293257 , vital:57069 , xlink:href="https://doi.org/10.1080/00958979908054907"
- Description: Spectroscopic changes observed on addition of nitrite to solutions of cobalt(II) tetra-sulfophthalocyanine ([Co(II)TSPc]4-) in the presence of N− 3 or ClO− 4 are reported. There is spectroscopic evidence for the oxidation of [Co(II)TSPc]4- to a [Co(III)TSPc]3- species in the presence of nitrite ions. Equilibrium and kinetic studies for the interaction between [Co(II)TSPc]4- and NO− 2 are reported. The rate was found to be first order in both [Co(II)TSPc]4- and NO− 2. The rate constant for the forward reaction, k f=1.6 × 10−4 dm3mol−1s−1 was determined at 20°C for the interaction between nitrite ions and [Co(II)TSPc]4- in the presence of NO3 − or ClO4 − ions.
- Full Text:
- Authors: Chebotareva, Natalia , Nyokong, Tebello
- Date: 1999
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293257 , vital:57069 , xlink:href="https://doi.org/10.1080/00958979908054907"
- Description: Spectroscopic changes observed on addition of nitrite to solutions of cobalt(II) tetra-sulfophthalocyanine ([Co(II)TSPc]4-) in the presence of N− 3 or ClO− 4 are reported. There is spectroscopic evidence for the oxidation of [Co(II)TSPc]4- to a [Co(III)TSPc]3- species in the presence of nitrite ions. Equilibrium and kinetic studies for the interaction between [Co(II)TSPc]4- and NO− 2 are reported. The rate was found to be first order in both [Co(II)TSPc]4- and NO− 2. The rate constant for the forward reaction, k f=1.6 × 10−4 dm3mol−1s−1 was determined at 20°C for the interaction between nitrite ions and [Co(II)TSPc]4- in the presence of NO3 − or ClO4 − ions.
- Full Text:
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