Use of cobalt (II) phthalocyanine to improve the sensitivity and stability of glassy carbon electrodes for the detection of cresols, chlorophenols and phenol
- Mafatle, Tsukutlane J, Nyokong, Tebello
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293335 , vital:57076 , xlink:href="https://doi.org/10.1016/S0003-2670(97)00464-9"
- Description: A cobalt(II) phthalocyanine-modified glassy carbon electrode (CoPc-GCE) was used for the detection of o-, m- and p-cresols, and of 2-chlorophenol, 4-chlorophenol and phenol. Modification of the glassy carbon electrode with CoPc increases the oxidation currents of these species and increases the stability of the electrode. CoPc-GCE showed less fouling by the oxidation products of these compounds than the unmodified GCE. Comparison of some first row transition metal phthalocyanines showed the following trend for the enhancement of the currents for the oxidation of cresols and phenols: Co(II)Pc > Mn(II)Pc > Fe(II)Pc > Ni(II)Pc > Cu(II)Pc > H2Pc > Zn(II)Pc > GCE. When [Co(II)TSPc]4− (TSPc=tetrasulfo Pc) was added to aqueous solutions containing the cresols and phenols, an enhancement of the oxidation currents was also observed.
- Full Text:
- Date Issued: 1997
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293335 , vital:57076 , xlink:href="https://doi.org/10.1016/S0003-2670(97)00464-9"
- Description: A cobalt(II) phthalocyanine-modified glassy carbon electrode (CoPc-GCE) was used for the detection of o-, m- and p-cresols, and of 2-chlorophenol, 4-chlorophenol and phenol. Modification of the glassy carbon electrode with CoPc increases the oxidation currents of these species and increases the stability of the electrode. CoPc-GCE showed less fouling by the oxidation products of these compounds than the unmodified GCE. Comparison of some first row transition metal phthalocyanines showed the following trend for the enhancement of the currents for the oxidation of cresols and phenols: Co(II)Pc > Mn(II)Pc > Fe(II)Pc > Ni(II)Pc > Cu(II)Pc > H2Pc > Zn(II)Pc > GCE. When [Co(II)TSPc]4− (TSPc=tetrasulfo Pc) was added to aqueous solutions containing the cresols and phenols, an enhancement of the oxidation currents was also observed.
- Full Text:
- Date Issued: 1997
Electrocatalytic oxidation of cysteine by molybdenum (V) phthalocyanine complexes
- Mafatle, Tsukutlane J, Nyokong, Tebello
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293369 , vital:57079 , xlink:href="https://doi.org/10.1016/0022-0728(95)04519-8"
- Description: Chemically modified electrodes, constructed by incorporating oxomolybdenum(V) phthalocyanine (OMo(V)(OH)Pc, Pc = phthalocyanine dianion) into graphite powder were used to catalyse the oxidation of cysteine. Solution catalysis of cysteine by oxomolybdenum(V) tetrasulfophthalocyanine, [OMo(V)(OH)TSPc]4−, was also investigated. A considerable reduction in overpotential for cysteine oxidation was observed. Cysteine oxidation occurred at 0.26 and 0.28 V vs. Ag/vbAgCl for catalysis by Omo(V)(OH)Pc and [OMo(V)(OH)TSPc]4− respectively as opposed to 0.77 V vs. Ag/vbAgCl observed on CoPc chemically modified electrodes. The anodic peak currents vary linearly with cysteine concentration in the range 0.02 to 0.08 mol dm−3 and 0.008 to 0.02 mol dm−3 for [OMo(V)(OH)TSPc]4− and OMo(V)Pc respectively.
- Full Text:
- Date Issued: 1996
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293369 , vital:57079 , xlink:href="https://doi.org/10.1016/0022-0728(95)04519-8"
- Description: Chemically modified electrodes, constructed by incorporating oxomolybdenum(V) phthalocyanine (OMo(V)(OH)Pc, Pc = phthalocyanine dianion) into graphite powder were used to catalyse the oxidation of cysteine. Solution catalysis of cysteine by oxomolybdenum(V) tetrasulfophthalocyanine, [OMo(V)(OH)TSPc]4−, was also investigated. A considerable reduction in overpotential for cysteine oxidation was observed. Cysteine oxidation occurred at 0.26 and 0.28 V vs. Ag/vbAgCl for catalysis by Omo(V)(OH)Pc and [OMo(V)(OH)TSPc]4− respectively as opposed to 0.77 V vs. Ag/vbAgCl observed on CoPc chemically modified electrodes. The anodic peak currents vary linearly with cysteine concentration in the range 0.02 to 0.08 mol dm−3 and 0.008 to 0.02 mol dm−3 for [OMo(V)(OH)TSPc]4− and OMo(V)Pc respectively.
- Full Text:
- Date Issued: 1996
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