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Anodic polarography of sugars at a platinized platinum electrode /Levitsky, Michael January 1952 (has links)
No description available.
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Polarographic study of hydroperoxides and hydrogen peroxide in hydrocarbon combustion products /Urone, Paul January 1954 (has links)
No description available.
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Amperometric nonaqueous titrations of the thenoyltrifluoroacetonates of some metals with sodium diethyldithiocarbamate as titrantFung, Dorcas May-Ling. January 1978 (has links)
No description available.
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Square-wave voltammetric stripping detection for flow injection analysis and chromatographyZhang, Li Qun 05 1900 (has links)
No description available.
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A study of ion pairing in the cadmium (II) - ethylene bis(oxyethylenenitrilo) N,N,N',N' tetraacetic acid - potassium nitrate systemShackelford, Walter McDonald 12 1900 (has links)
No description available.
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Amperometric nonaqueous titrations of the thenoyltrifluoroacetonates of some metals with sodium diethyldithiocarbamate as titrantFung, Dorcas May-Ling. January 1978 (has links)
No description available.
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Validation of chemical speciation modelsJarratt, Jason Aldrin January 1998 (has links)
No description available.
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Study of the chemical reaction preceding reduction of CdNTA complexes using stationary electrode polarographyShuman, Mark S. January 1966 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1966. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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Properties of polarographic electrodes with renewed surface. Pt. 1. Mercury thread electrodes. Pt. 2. Pulsed mercury electrodesRosenberg, Norman January 1956 (has links)
Thesis (Ph.D.)--Boston University / The most common polagraphic electrode in use at the present time is the dropping mercury electrode (DME). There are, however, certain well-recognized disadvantages attendant on the use of the DME: (1) oxidation analysis is limited to 0.4 v.; (2) there are rather large charging currents associated with the growing drop; (3) the area of the drops, and hence the sensitivity can not be appreciably increased; (4) because of drop growth, a a spiky sort of current is obtained which introduces a reading error into the results obtained, especially at low concentrations. It can be seen that these disadvantages are largely a function either of the electrode shape and size, or of the method of electrode propagation. [TRUNCATED]
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A critical study of the determination of molybdenum in plant materialGore, William Tompson January 1961 (has links)
1. Polarographic and spectrophotometric methods for the determination of molybdenum were reviewed. 2. The inclusion of salicylaldoxine in several supporting electrolytes was examined with a view to developing a polarographic procedure, suitable for routine analyses, which did not necessitate a preliminary time-consuming separation stage. A stable molybdenum wave was obtained from an electrolyte having a composition similar to the test solution obtained after the wet digestion of plant material. The height of the wave was found to be, over an optimum range, independent of the reagent concentrations. The wave was however distorted by a maximum, which rendered it unsuitable for quantitative analytical application. 3. The spectrophotometric procedure for molybdenum using thiocyanate is virtually specific and was examined critically. Modifications were found to improve the sensitivity of the procedure, and the stability of the chromatic compound. 4. The modified spectrophotometric procedure is recommended for the routine determination of molybdenum in plant material.
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