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Polarography cadmium

To overcome some of the problems associated with aqueous media, non-aqueous systems with cadmium salt and elemental sulfur dissolved in solvents such as DMSO, DMF, and ethylene glycol have been used, following the method of Baranski and Fawcett [48-50], The study of CdS electrodeposition on Hg and Pt electrodes in DMSO solutions using cyclic voltammetry (at stationary electrodes) and pulse polarography (at dropping Hg electrodes) provided evidence that during deposition sulfur is chemisorbed at these electrodes and that formation of at least a monolayer of metal sulfide is probable. Formation of the initial layer of CdS involved reaction of Cd(II) ions with the chemisorbed sulfur or with a pre-existing layer of metal sulfide. [Pg.93]

Savvaidis I, Hughes M, Poole R (1992) Differential pulse polarography a method of directly measuring uptake of metal ions by live bacteria without separation of biomass and medium. FEMS Microbiol Lett 92 181-186 Savvaidis I, Hughes MN, Poole RK (2003) Copper biosorption by Pseudomonas cepacia and other strains. World J Microbiol Biotechnol 19 117-121 Scott JA, Palmer SJ (1988) Cadmium biosorption by bacterial exopolysaccharide. Biotechnol Lett 10 21-24... [Pg.96]

Day 2 for lead, cadmium, copper, cobalt, and nickel by Chelex extraction and differential pulse polarography, as well as manganese by Chelex and flameless atomic absorptiometry. [Pg.33]

Mercury was determined after suitable digestion by the cold vapour atomic absorption method [40]. Lead was determined after digestion by a stable isotope dilution technique [41-43]. Copper, lead, cadmium, nickel, and cobalt were determined by differential pulse polarography following concentration by Chelex 100 ion-exchange resin [44,45], and also by the Freon TF extraction technique [46]. Manganese was determined by flameless atomic absorption spectrometry (FAA). [Pg.34]

Stolzberg [143] has reviewed the potential inaccuracies of anodic stripping voltammetry and differential pulse polarography in determining trace metal speciation, and thereby bio-availability and transport properties of trace metals in natural waters. In particular it is stressed that nonuniform distribution of metal-ligand species within the polarographic cell represents another limitation inherent in electrochemical measurement of speciation. Examples relate to the differential pulse polarographic behaviour of cadmium complexes of NTA and EDTA in seawater. [Pg.151]

In a method described by Yoshimura and Uzawa [ 144], cadmium in seawater is coprecipitated with zirconium hydroxide (Zr(OH)4) prior to determination by square-wave polarography. The precipitate is dissolved in hydrochloric acid, and cadmium concentration is determined from the peak height of the... [Pg.151]

Kounaves and Zirino [ 145] studied cadmium-EDTA complex formation in seawater using computer-assisted stripping polarography. They showed that the method is capable of determining the chemical speciation of cadmium in seawater at concentrations down to 10 8 M. [Pg.152]

Stolzberg [143] has discussed potential inaccuracies in trace metal speciation measurement in the determination of copper and cadmium by differential pulse polarography and ASV. [Pg.290]

Cadmium Co-precipitation with zirconium hydroxide, dissolution of Square wave polarography at precipitate in hydrochloric acid -0.6 V [144]... [Pg.291]

It has been established by polarography that cadmium(n) and mercury)n) form 1 1 and 2 1 complexes with vitamin B6.266 Activation parameters are reported. [Pg.467]

Determination of Zinc in Cadmium by Square-Wave Polarography. [Pg.151]

Calcium Chloride Solution. III. The Polarography of Copper Cadmium, Iron and Manganese. Anal. Chim. Acta 9, 91 (1953). [Pg.157]

Cadmium was determined by polarography at the dropping mercury electrode in solutions that were 1 ... [Pg.705]

Polarography can be used for the determination of cadmium with other metals (Cu, Ni, Zn) at concentrations of tenth and even hundredths mg 1. ... [Pg.311]

Chemical analysis provides much more precise data about the sample, particularly the determination of metallic elements, mainly lead, cadmium, iron, calcium, sodium as well a.s anions, chlorides, fluorides, nitrates, carbonates and sulphates. The analyses are performed most frequently by spectrophotometry, atomic absorption spectrometry, or polarography in recent years radionuclide X-ray fluorescence and activation analysis have been used. [Pg.596]

Baric, A. and Branica, M., 1967. Polarography of sea water I, ionic state of cadmium and... [Pg.213]

Some of the earliest work utilizing polarography for water analysis was done by Heller and co-workers in 1935 (J9). They determined as little as 0.01 mg./liter of copper, bismuth, lead cadmium, and zinc polarographically after extraction with dithizone and carbon tetrachloride. This work also described conditions of extraction for minimizing interferences in certain cases. [Pg.173]

Brass contains about 657o copper and 307o zinc. Would you suggest polarography as a method for determining the main components When and why The alloy contains also 1 % or less of lead and cadmium. Is polarography useful for those metals Explain why or why not. [Pg.90]

Recently, stationary electrode polarography has been used to study the electrode kinetics of several metal-ion systems on mercury in DMSO solutions. In cadmium discharge, the rate-determining step was believed to be a chemical reaction, the loss of molecules of solvation from the reactant ion, preceding a reversible charge transfer. The sensitivity of the rate towards the electrolyte cation suggests that the slow step is essentially confined to the double layer. [Pg.775]

Other techniques that have been used for the examination of organometallic stabilisers extracted from PVC include column chromatography (barium, cadmium and zinc salts of fatty acids [125]), paper chromatography (cadmium, lead and salts of fatty acids [126]), polarography (cadmium, lead and zinc salts [127]), spectroscopy (cadmium, lead and zinc salts [128]) chemoluminescence techniques and flame photometry (sodium, potassium, barium, cadmium and lead salts [129]). [Pg.127]

Like zinc ions, cadmium ions can be titrated in buffered solutions with EDTA but the end-point is more easily located by high frequency titration than by an indicator. Among the instrumental methods suitable for the determination of cadmium in dilute solutions, atomic absorption is ideal and polarography is also suitable. Gravimetrically, cadmium can be precipitated as the oxinate similar to zinc. In addition, it can be precipitated as molybdate. [Pg.233]


See other pages where Polarography cadmium is mentioned: [Pg.422]    [Pg.422]    [Pg.858]    [Pg.671]    [Pg.672]    [Pg.415]    [Pg.438]    [Pg.572]    [Pg.534]    [Pg.42]    [Pg.47]    [Pg.209]    [Pg.1055]    [Pg.89]    [Pg.534]    [Pg.294]    [Pg.585]    [Pg.207]    [Pg.135]    [Pg.176]    [Pg.176]    [Pg.272]    [Pg.174]    [Pg.5045]    [Pg.4013]    [Pg.344]    [Pg.520]    [Pg.788]   
See also in sourсe #XX -- [ Pg.378 , Pg.380 ]




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