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The Application of the Galvanic Cell Oxygen Analyzer to Waste Control Programs K. H. MANCY, Research Fellow W. C. WESTGARTH, Research FeUow and D. A. OKUN, Professor of Sanitary Engineering Department of Sanitary Engineering School of Public Health University of North Carolina Chapel Hill, North Carolina Investigations in the Department of Sanitary Engineering of the University of North Carolina School of Public Health at Chapel Hill have led to the development of a galvanic cell oxygen analyzer for indicating and monitoring dissolved oxygen in natural waters and wastes. The theory of operation of this instrument and consideration in its design have been presented elsewhere (1, 2, 3). Electroactive and surface active impurities in solutions interfere with the electrode reaction kinetics of exposed metal electrodes. Clark showed that this interference is eliminated by covering the sensing electrode with a plastic membrane permeable to oxygen (and other gases in general) but practically impermeable to ionic species in the test solution (4). Later, Carritt and Kanwisher devised a temperature-compensated electrode system composed of a membrane-covered platinum cathode and silver-silver oxide anode (5). Electrode systems based on the galvanic cell principle have been used in Europe by Todt (6) and Husmann and Stracke (7) for the determination of dissolved oxygen in rivers. In an attempt to minimize the poisoning effect of impurities in the test solution, mechanically-driven blades were used to scrape the electrode surface continuously. The galvanic cell oxygen analyzer consists of a silver-lead galvanic couple separated from the test sample by a plastic membrane. The generated current is directly proportional to the oxygen content in the sample. This paper describes its construction, characteristics, and some applications in the sanitary engineering field. PRINCIPLE OF THE GALVANIC CELL OXYGEN ANALYZER Oxygen-sensitive galvanic cells can be designed so that the generated current is proportional to the oxygen concentration in contact with the cathode. In such an electrode system an outer source of applied voltage is not needed. The basic design factors of an oxygen-sensitive galvanic cell are: 1) The anode material must consist of a relatively basic metal of reasonable stability, which has no tendency toward passivation (e. g., zinc, lead, cadmium; 2) The supporting electrolyte must consist of a well-conducting electrolyte solution which does not dissolve the anode metal at any significant - 508 -
Object Description
Purdue Identification Number | ETRIWC196242 |
Title | Application of the galvanic cell oxygen analyzer to waste control programs |
Author |
Mancy, K. H. Westgarth, W. C. Okun, Daniel Alexander |
Date of Original | 1962 |
Conference Title | Proceedings of the seventeenth Industrial Waste Conference |
Conference Front Matter (copy and paste) | http://earchives.lib.purdue.edu/cdm4/document.php?CISOROOT=/engext&CISOPTR=9369&REC=18 |
Extent of Original | p. 508-523 |
Collection Title | Engineering Technical Reports Collection, Purdue University |
Repository | Purdue University Libraries |
Rights Statement | Digital object copyright Purdue University. All rights reserved. |
Language | eng |
Type (DCMI) | text |
Format | JP2 |
Date Digitized | 2009-05-18 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Resolution | 300 ppi |
Color Depth | 8 bit |
Description
Title | page 508 |
Collection Title | Engineering Technical Reports Collection, Purdue University |
Repository | Purdue University Libraries |
Rights Statement | Digital object copyright Purdue University. All rights reserved. |
Language | eng |
Type (DCMI) | text |
Format | JP2 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Transcript | The Application of the Galvanic Cell Oxygen Analyzer to Waste Control Programs K. H. MANCY, Research Fellow W. C. WESTGARTH, Research FeUow and D. A. OKUN, Professor of Sanitary Engineering Department of Sanitary Engineering School of Public Health University of North Carolina Chapel Hill, North Carolina Investigations in the Department of Sanitary Engineering of the University of North Carolina School of Public Health at Chapel Hill have led to the development of a galvanic cell oxygen analyzer for indicating and monitoring dissolved oxygen in natural waters and wastes. The theory of operation of this instrument and consideration in its design have been presented elsewhere (1, 2, 3). Electroactive and surface active impurities in solutions interfere with the electrode reaction kinetics of exposed metal electrodes. Clark showed that this interference is eliminated by covering the sensing electrode with a plastic membrane permeable to oxygen (and other gases in general) but practically impermeable to ionic species in the test solution (4). Later, Carritt and Kanwisher devised a temperature-compensated electrode system composed of a membrane-covered platinum cathode and silver-silver oxide anode (5). Electrode systems based on the galvanic cell principle have been used in Europe by Todt (6) and Husmann and Stracke (7) for the determination of dissolved oxygen in rivers. In an attempt to minimize the poisoning effect of impurities in the test solution, mechanically-driven blades were used to scrape the electrode surface continuously. The galvanic cell oxygen analyzer consists of a silver-lead galvanic couple separated from the test sample by a plastic membrane. The generated current is directly proportional to the oxygen content in the sample. This paper describes its construction, characteristics, and some applications in the sanitary engineering field. PRINCIPLE OF THE GALVANIC CELL OXYGEN ANALYZER Oxygen-sensitive galvanic cells can be designed so that the generated current is proportional to the oxygen concentration in contact with the cathode. In such an electrode system an outer source of applied voltage is not needed. The basic design factors of an oxygen-sensitive galvanic cell are: 1) The anode material must consist of a relatively basic metal of reasonable stability, which has no tendency toward passivation (e. g., zinc, lead, cadmium; 2) The supporting electrolyte must consist of a well-conducting electrolyte solution which does not dissolve the anode metal at any significant - 508 - |
Resolution | 300 ppi |
Color Depth | 8 bit |
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