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1. |
An amperometric solid‐state sensor for Nitrogen dioxide based on a solid polymer electrolyte |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 133-138
František Opekar,
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摘要:
AbstractA new sensor is described consisting of a Nafion membrane to which a very fine gold square grid indicator electrode is mechanically pressed. A platinum counter and a Pt/air reference electrode are prepared on the membrane using a chemical plating method. Nitrogen dioxide was determined in air by reduction at −0.3V vs. Pt/air electrode (0.75 V vs. SHE). The response dependence on the NO2concentration was linear, with a sensitivity of 59 nA.ppm−1(42% rel. humidity). The time constant and the time required to attain 95% of the steady ‐state response were 2.2 and 10 s, respectively. The response was independent of the air flow rate, but increased linearly with increasing relative humidity. The sensor sensitivity decreased with time–the longer the sensor was in contact with NO2. The decrease amounted to ca. 5% per 24 hours during constant exposure to NO2. The indicator electrode can be reactivated by cyclic polarization. On the basis of the sensitivity attained, the indicator electrode can be considered as an array of microband ele
ISSN:1040-0397
DOI:10.1002/elan.1140040202
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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2. |
Photoelectrochemical detection and speciation of thallium (I) and thallium (III) |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 139-142
Joseph N. Barisci,
Gordon G. Wallace,
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摘要:
AbstractA method that allows speciation and electrochemical detection of thallium in flowing solutions has been developed. Thallous ions are determined using oxidative detection at a platinum electrode in a sulphuric acid‐formic acid solution. In the presence of thallic ions, iiradiation of the solution with UV light induces the reduction of Tl(III) to Tl(I) which is subsequently detected as described above. Under these conditions total thallium is determined. Irradiation of the flowing solution is carried out within the detector flow cel
ISSN:1040-0397
DOI:10.1002/elan.1140040203
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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3. |
Voltammetric investigations of copper processes in the presence of oxygen |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 143-150
Damir Krznarić,
Marta Plavšić,
Božena Ćosović,
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摘要:
AbstractThe redox processes of copper ions were studied by alternating current (ac) voltammetry and cyclic voltammetry in 0.5 M NaCl and NaClO4solutions. The studies were performed at different pH values in the presence of atmospheric oxygen or by the addition of H2O2to the process. In the case of copper ions in NaCl solution both in the presence of atmospheric oxygen and added H2O2, a catalytic current was observed. With cyclic voltammetry the current was in the cathodic direction in spite of having an anodic sweep. The key factor is the presence of chloride ions as in the NaClO4solution; the observed catalytic current peaks are much smaller. The mechanism for the observed redox processes of copper is proposed.
ISSN:1040-0397
DOI:10.1002/elan.1140040204
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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4. |
Characterization of uranyl‐monoperoxo species in 0.7 mol L−1LiCIO4 |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 151-159
Renata Djogic,
Marko Branica,
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摘要:
AbstractAccording to the calculations, in the presence of equimolar concentrations of uranyl‐ion and hydrogen peroxide at 5
ISSN:1040-0397
DOI:10.1002/elan.1140040205
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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5. |
Automated system for on‐line adsorptive stripping voltammetric monitoring of trace levels of uranium |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 161-165
Joseph Wang,
Rossi Setiadji,
Liang Chen,
Jianmin Lu,
Stephen G. Morton,
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摘要:
AbstractAn automated system for on‐line monitoring of trace uranium, based on a flow‐through adsorptive stripping operation, is described. The on‐line formation of the uranium‐oxine complex is followed by its adsorptive accumulation and voltammetric quantitation at the downstream working electrode. About 10–60 runs can be made every hour with high reproducibility (RSD of 3–5%) and a detection limit of 0.7 μg/L. The dependence of the peak current on different experimental variables is reported. The sequence of events involved in the adsorptive stripping voltammetric cycle is controlled by a computer. Analogous on‐line monitoring of chromium (VI) are also reported with 36 runs/h (2.1% RSD), and detection limit of 1.5 μg/L. The system holds great promise for field
ISSN:1040-0397
DOI:10.1002/elan.1140040206
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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6. |
Homogeneous catalysis of electrochemical reactions. Channel electrode voltammetry and the EC′ mechanism |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 167-182
Richard G. Compton,
Adrian C. Fisher,
R. Anthony Spackman,
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摘要:
AbstractThe shape of the current–voltage curves at a channel electrode have been calculated for the various situations of the catalytic (EC′) mechanism. In particular the halfwave potential and limiting current are found to be highly sensitive to the solution‐flow rate and to the concentrations of the mediator and substrate employed. These observations provide a ready method of unambiguously characterizing the different pat
ISSN:1040-0397
DOI:10.1002/elan.1140040207
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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7. |
Liquid chromatography amperometric detection of catechol, resorcinol, and hydroquinone with a copper‐based chemically modified electrode |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 183-189
Jianxun Zhou,
Erkang Wang,
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摘要:
AbstractA copper‐based chemically modified electrode (CME) has been constructed and characterized for flow‐through amperometric detection of catechol, resorcinol, and hydroquinone. Novel potential dependence of the detector response was first obtained for these analytes at the Cu CME, where negative peaks together with positive ones were observed in one definite chromatogram using amperometric detection. Its advantages in chromatographic applications were demonstrated. From these observations it is proposed that the detector response was governed by formation of copper complexes with the solutes. A dynamic linear range over two orders of magnitude was obtained, when operating the detector at +0.10 V vs. SCE, from which ng detection limits were achie
ISSN:1040-0397
DOI:10.1002/elan.1140040208
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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8. |
Electrochemical oxidation ofL‐ascorbic acid at the graphite electrode and its monitoring by a thick‐film graphite sensor assembly |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 191-197
Xuekun Xing,
Thiam‐Chye Tan,
Meijun Shao,
Chung‐Chiun Liu,
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摘要:
AbstractThe experimental results obtained in this study show that a thick‐film graphite sensor assembly (with a Pt counter and an Ag/AgCl reference electrode) can be conveniently fabricated by the photolithographic and screen‐print metallization techniques. This sensor has been successfully employed for quantitatively determiningL‐ascorbic acid concentration in aqueous solutions with reasonably good reproducibility. This sensor provides the possibility of developing a miniature size practical device for detecting ascorbic acid in biochemical processing, such as in food and drug production. The mechanistic aspects of the oxidation ofL‐ascorbic acid on optical pyrolytic graphite electrodes were further studied with a rotating OPG disk electrode in two different electrolyte solutions. It was found that the oxidation ofL‐ascorbic acid is more favored in pH = 7 solutions than in pH = 1 solutions although a common 2‐electron transfer pathway is applied in
ISSN:1040-0397
DOI:10.1002/elan.1140040209
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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9. |
Polarographic studies and measurements of nitrite in cobalt(II)—thiocyanate—ascorbic acid solution |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 199-206
Peibiao Li,
Zaofan Zhao,
Zhiqiang Gao,
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摘要:
AbstractIn the cobalt(II)—thiocyanate—ascorbic acid solution (pH = 2.0), nitrite can form a ternary complex (CoSCNNO)+, which can be reduced at mercury electrode to −0.59 V (vs. SCE). The wave can be used for the polarographic determination of traces of nitrite in the concentration range of 1 × 10−8−8 × 10−7M (single sweep polarography), 1 × 10−7−4 × 10−5M (differential pulse polarography). or 1.5 × 10−6−2 × 10−4M (direct current polarography). The mechanism of the electrode process is studied by linear sweep voltammetry, DC polarography, cyclic voltammetry, double‐step chronocoulometry, and controlled potential coulometry. The polarographic wave is ascribed to the reduction of nitrogen monoxide in the complex to hydroxyamine. The procedure is used for the direct determination of
ISSN:1040-0397
DOI:10.1002/elan.1140040210
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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10. |
Electrochemical investigations of 3‐(p‐sulfamoylphenylhydrazono)‐2,4‐pentanedione at pyrolytic graphite electrode |
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Electroanalysis,
Volume 4,
Issue 2,
1992,
Page 207-216
R. N. Goyal,
Anoop Kumar,
Sandhya Bhargava,
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摘要:
AbstractThe electrochemical behavior of 3‐(p‐sulfamoylphenylhydrazono)‐2, 4‐pentanedione has been studied in the pH range 2.2–10.2. It was observed that sulfamoylphenylhydrazone undergoes electrooxidation as well as electroreduction at the surface of a pyrolytic graphite electrode (PGE). The oxidation or reduction peaks observed can be used for the detection of this compound. The products corresponding to both processes have been separated and characterized using IR, NMR, and mass spectra. The reaction pathways have been proposed to account for the voltammetric, coulometric and spectral
ISSN:1040-0397
DOI:10.1002/elan.1140040211
出版商:VCH Verlagsgesellschaft mbH
年代:1992
数据来源: WILEY
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