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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 58 (1986), S. 1498-1501 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1436-5073
    Keywords: chemically modified electrode ; electrochemical sensor ; flow injection analysis ; nitrite ; heptacyanonitrosylferrate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The electrocatalysis of nitrite in solutions at an inorganic film modified glassy carbon electrode was studied. The modifier was an electrodeposited thin inorganic film of the copper-heptacyanonitrosylferrate (CuHNF). Cyclic voltammetry of the modified electrode in a nitrite solution revealed that both oxidation and reduction of nitrite were catalyzed and the electrocatalytic currents were controlled by the diffusion of nitrite. Voltammetric and amperometric responses were investigated. When applied as an amperometric sensor in a flow injection system, the modified electrode permitted detection at — 0.55 V, over 500 mV lower than at the naked electrode surface. A linear response range extending from 1 × 10−6 to 1 × 10−3 M nitrite was obtained, with a detection limit of 3 × 10−7 M. The relative standard deviation for 50 repetitive injections with a 5 × 10−5 M nitrite solution was less than 4%. The procedure was applied to the determination of nitrite in saliva and nitrate.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 339 (1991), S. 137-141 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new preconcentration and voltammetric determination method for cobalt(II) in aqueous solution with a chemically modified electrode is proposed. The accumulation behaviour and voltammetry of cobalt(II) has been investigated with a carbon paste electrode modified with cationexchanger and 1,10-phenanthroline. The electrochemical response is characterized with respect to carbon paste composition, pH, preconcentration time, cobalt(II) concentration and other variables. For a 3-min preconcentration time, the electrode gives good linearity for 1×10−7 to 4×10−6 mol/l Co(II), a detection limit of 8×10−8 mol/l. The response can be reproduced with a 4.0% relative standard deviation. The method is fairly free from many coexisting ions interferences. A rapid and convenient renewal procedure allows the use of a single electrode in multiple analytical determinations over several days. Satisfactory results are obtained for the determination of cobalt in a variety of certified standard reference materials.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 139-146 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polarographic procedure is described for the determination of ammonia at concentration levels below 10-4 M that is based on its reaction with 1-naphthol and hypochlorite in a strongly alkaline medium whose (1,4-indonapthol) product is polarographically active. The polarographic behavior of the compound and the electrode process has been studied by several electrochemical methods. The experimental results showed that it is an EC process involving the formation of a radical as the electrode product that is followed by a disproportionation reaction of the radical. The rate constant (kf) of the coupled following chemical reaction was found to be 0.228 s-1. The wave height at -0.47 V [versus the standard calomel electrode (SCE)] on the dropping mercury electrode (DME) is directly proportional to the concentration of ammonia from 1 × 10-7 to 5 ×-5 M, and the detection limit is 5 × 10-8 M. A mercury film electrode can also be used for the determination of ammonia. The method has been applied to the analysis of water and serum samples.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 51-56 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using linear sweep polarography (LSP) in an acidic solution (pH 2.8) containing Au(III) ions and N-allyl-N′-(sodium-p-phenylsufonate)thiourea (NTu), the product of the reaction between Au(III) and NTu (NDF) is reducible at the mercury electrode with two waves at about -0.40 and -0.95 V [versus the saturated calomel electrode (SCE)]. In the presence of excess chloride, the potential of the first wave shifts positively to -0.35 V. This forms the basis of a highly selective and sensitive method for gold. The linear range for gold is from 1 × 10-7 to 3 × 10-M, and the detection limit is 5 × 10-8 M (9 ppb). This method has been used for the determination of gold in ore samples, and the results agree well with values obtained by accepted procedures. Various electrochemical techniques were used to study the mechanism of the redox process. The reaction mainly involves the formation of C,C′-di-N-allyl-N′- (sodium-p-phenysulfonate)dithiodiformamidine (NDF). Unlike some explanations reported in the literature about the reduction of formamidine derivatives (containing an —S—S— bond) on an Hg electuode, the electrode process for the first wave (-0.40 V) is ascribed to the reduction of the HgS film, which is caused by the reaction of Hg with adsorbed NDF. In the presence of excess Cl- ions, the mixed precipitation film of HgS·xHg2Cl2 may be formed on the electrode surface and make the first wave shift to -0.35 V. The second wave (-0.95 V) is caused by the irreversible reduction of NDF.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 1 (1989), S. 371-374 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A rapid, sensitive, selective single-sweep polarographic method for the determination of palladium based on the reduction of palladium(II) in the Pd(II)-dimethylglyoxime (DMG) complex is described. In weakly acidic media, Pd(II) reacts with DMG and forms a yellow precipitate. After adding a low concentration of the anionic surfactant SDBS (sodium dodecylbenzenesulfonate), the solubility of the complex increases remarkably, and the sensitivity of the determination increases more than fivefold. The solution is stable for at least 3 hours. The complex is strongly adsorbed on the surface of the mercury electrode. The enhancement effect of the surfactant is ascribed to the “synergistic adsorption” of the complex and the surfactant. The current is caused by the reduction of palladium in the complex at -0.45 V (versus SCE). The method can be used to determine trace amounts of palladium over the range of 4 × 10-8 to 4 × 10-6. Assays of palladium catalysts and waste water samples are illustrated.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1040-0397
    Keywords: Cobalt ; ultratrace measurements ; catalytic polarography ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In an acetate acid buffer solution (pH = 4.5) containing 2-(3,5-dibromo-2-pridyl)azo-5-diethylaminophenol or 3,5-2Br-PADAP and nitrite, there is a catalytic single-sweep polarographic peak that is very sensitive and selective to cobalt(II). The linear range is from 1 × 10-10 M to 1 × 10-6 M, with a detection limit of 5 × 10-11 M. Most common cations and anions do not interfere with the determination. The method has been used or the determination of trace cobalt in human hair and pure nickel nitrate samples. The mechanism involved has been investigated by various electrochemical methods, and the catalytic process is .
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 4 (1992), S. 199-206 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In 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 × 10-7 M (single sweep polarography), 1 × 10-7 -4 × 10-5 M (differential pulse polarography). or 1.5 × 10-6 -2 × 10-4 M (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 nitrite in various real samples.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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