Effect of citric acid and hydrochloric acid on the polarographic behaviour of tin: Application to the determination of tin(II) in presence of tin(IV) in the activating solutions of the electroless plating of polymers

A new method for the determination of tin(II) in presence of tin(IV) is described. The method is based on differential pulse polarography on the hanging mercury drop electrode (HMDE). The effect of citric acid and hydrochloric acid concentrations on the polarographic peaks of tin(II) and tin(IV) has been studied. In 1 M HCl, the total quantity of tin can be determined, as under these conditions, in the absence of complexing agents, eventual variations in the oxidation states, in any concentration ratio, do not affect the peak height and the peak potential. In 0.2 M HCl and 0.2 M citric acid, tin(II) can be determined selectively in presence of tin(IV), as under these conditions, tin(IV) does not present polarographic response, while a well-defined peak is observed for tin(II). The method is applied to determine tin(II) and total tin in the activating solutions of the electroless plating of polymers.     

Coulometric determination of lead(II) and lead(IV) in high-T c superconductors containing copper and bismuth

The behavior of Pb(II) and Pb(IV) was studied by voltammetry in supporting electrolytes containing 0.1 M NaOH or 0.1 M NaOH + 0.1 M Na₃Cit at a graphite and a mercury thin-film electrodes. The best conditions were found for the coulometric determination of Pb by the oxidation of Pb(0) to Pb(II) in the presence of 5- to 20-fold amounts of Bi(III) and Cu(II) within the range 0.2–2 mg Pb(II) with an error and a relative standard deviation of less than 0.5%. Along with the procedure proposed previously for the determination of Pb(II) and Pb(IV) present simultaneously using a platinum gauze electrode, this procedure was applied to the determination of Pb(II) and Pb(IV) in samples of high-T_c. Cu-Bi superconductors. For samples of high-T_c. Bi-Pb-A-Cu-0 superconductors (A = Ba or Sr-Ca) containing from 2 to 12% Pb(II), the relative standard deviation was less than 0.5%; for 0.6–7% Pb(IV), it was 1-0.2%.     

Electrolytically generated silver(II) as a coulometric titrant

The use of electrolytically generated silver(II) as a coulometric titrant has been studied. Difficulties arising from the current efficiency for generation of silver (II) at a platinum or gold electrode and from the reduction of silver(II) by water, have been overcome. The precautions necessary for accurate titrations of oxalic acid, cerium(III), arsenic(III) and vanadium(IV) by amperometric or potentiometric methods are detailed. Manganese and chromium could not be determined directly. Substances which reduce nitric acid could be determined if care was taken.     

Electroreduction of uranium (VI) at a platinum electrode and its analytical applications

Under normal conditions, the reduction of uranium(VI) at a platinum electrode, in acid solutions, is masked by the reduction of the hydrogen ion. If the working electrode is subjected to hydrogen evolution (at a current density of about 7 A cm (2) for 90-120 min) the H(ads) on the platinum surface, acting as a bridge in the electron transfer, shifts the reduction wave of uranium(VI), in 1M sulphuric acid solutions, to potentials (E(1 2 ) congruent with - 0.03 V) less negative than that of the hydrogen discharge (about -0.25 V). The wave corresponding to the reduction of uranium(VI) to uranium(IV) is well shaped, diffusion-controlled, and can be used for the determination of uranium down to 2 x 10(-5)M or 3 x 10(-6)M if a rotating electrode is used. Interferences arise from those ions with similar E(1 2 ) [i.e., Cu(II) and Bi(III)], or from those such as permanganate and dichromate, which oxidize the H(ads) on the platinum electrode. Because of the time required for the electrode pretreatment, the determination is time-consuming but in some respects it appears a useful improvement over the DME.     

Adsorptive stripping voltammetric measurements of trace amounts of platinum(II) and ruthenium(III) in the presence of 1-(2-pyridylazo)-2-naphthol

An extremely sensitive stripping voltammetric procedure for low level measurements of platinum (II, IV) or ruthenium (III, IV) is reported. The method is based on the interfacial accumulation of the platinum (II) or ruthenium (III)-1-(2-pyridylazo)-2-naphthol complex on the surface of a hanging mercury drop electrode, followed by the reduction of the adsorbed complex during the cathodic scan. The peak potential was found to be –0.8 V vs. Ag/AgCl electrode and the reduction current of the adsorbed complex ions of platinum (II) or ruthenium (III) was measured by differential pulse cathodic stripping voltammetry. The optimum experimental conditions were: 1.5×10^–7 mol/l of 1-(2-pyridylazo)-2-naphthol solution of pH 9.3, preconcentration potential of –0.2 V, accumulation time of 3 min and pulse amplitude of 50 mV with 4 mV s^–1 scan rate in the presence of ethanol-water (30% v/v) — sodium sulphate (0.5 mol/l). Linear response up to 6.4 × 10^–8 and 5.1 × 10^–8 mol/l and a relative standard deviation (at 1.2×10^–8 mol/l) of 2.4 and 1.6% (n=5) for platinum (II) and ruthenium (III) respectively were obtained. The detection limits of platinum and ruthenium were 3.2×10^–10 and 4.1×10^–10 mol/l, respectively. The electronic spectra of the Pt(II) — PAN and Ru(III) — PAN complexes were measured at pH 9.3 and the stoichiometric ratios of the complexes formed were obtained by the molar ratio method. The effects of some interfering ions on the proposed procedure were critically investigated. The method was found suitable for the sub-microdetermination of ruthenium (IV) and platinum (IV) after their reduction to ruthenium (III) and platinum (II) with sulphur dioxide in acid media. The applicability of the method for the analysis of binary mixtures of ruthenium (III) and (IV) or platinum (II) and (IV) has also been carried out successfully. The method is simple, rapid, precise, and promising for the determination of the tested metal ions at micro-molar concentration level.     

The coulometric generation of manganese(II) from a manganese electrode: : The Titration of EDTA

The anodic behavior of a manganese electrode is discussed. Manganese(II) can be generated with greater than 95% current efficiency over a limited current density range in neutral aqueous and methanolic chloride media. The current efficiency for the generation of manganese(II) as a function of current density, supporting electrolyte, solvent, pH, and generation time is given. Electrogenerated manganese(II) is useful in the coulometric titration of 4.460 × 10^-6–2.214 × 10^-5 mol of EDTA in 1.0 M sodium chloride buffered at pH 5.5. The end-point can be detected amperometrically by monitoring the anodic current from the oxidation of manganese(II) at platinum. The titration error is about 1% in replicate determinations. Permanganate can be generated in aqueous sodium hydroxide media but the current efficiencies are less than 20% and irreproducible.     

Voltammetric Determination of Tin(II) and Iron(II) on Mechanically Renewed Graphite Electrode in Tin-Plating Electrolyte

The analytical properties of the cathodic peak of tin(II) reduction and the anodic peak of iron(II) oxidation on a graphite electrode were studied with the electrode surface mechanically renewed directly in a solution before applying a potential in each measurement. The influence of the organic components of the phenolsulfonic tin-plating electrolyte on the cathodic current of tin(II) reduction and anodic current of iron(II) oxidation was studied. A dc voltammetric method was proposed for determining tin(II) directly in the phenolsulfonic tin-plating electrolyte, and iron(II) after the electrolyte is diluted tenfold with a 0.5M H₂SO₄ supporting solution.     

Electroreduction of molybdenum(VI) at a prehydrogenated platinum electrode

The use of hydrogenated platinum electrodes allows observation of the electroreduction of some oxygenated ions, which is otherwise masked by the reduction of the hydrogen ion. The present paper deals with the reduction of molybdenum(VI) at a prehydrogenated platinum electrode in acid solutions. The experimental conditions for the electrode hydrogenation process are the following: 90 min at a cathodic current density of about 7 A/cm(2) for microelectrodes with an area of 0.02-0.03 cm(2); about 120 min at a current density of 1.5-2 A/cm(2) for microelectrodes with an area of 0.25-0.35 cm(2). The reduction of molybdenum(VI) in 0.8-1.6M H(2)SO(4) occurs in two consecutive steps: the more cathodic wave [Mo(V) to Mo(III)] is for the most part masked by the reduction of the solvent; the less cathodic wave [Mo(VI) to Mo(V)] takes place at E(1 2 ) values of about +0.07 V, is well shaped, diffusion-controlled and usable for the determination of molybdenum down to 4 x 10(-5)M or 6 x 10(-5)M if a rotating disk electrode is used. Interferences from diverse ions have been studied. A generalization of the effect of electrode hydrogenation on the reduction of those oxygenated ions so far studied [i.e., vanadium(IV), uranium(VI) and molybdenum(VI)] is presented.     

Electrogeneration of gold(III) in halide media

Gold(III) was electrogenerated with high efficiency at constant current in halide media by oxidation of freshly electrodeposited gold on a platinum electrode. The electrolytes tested were 0.0005–1 M HCl, NaCl HBr, and NaBr. Potentiometric studies indicated that the tetrahaloaurate(III) complex was generated in each case with oxidation potentials ranging from 0.83 to 1.15 V. Arsenic(III) (20 μeq) was titrated potentiometrically in 0.1 M NaBr by using a gold indicating electrode; the efficiency was 99.90 ± 0.05%. Iron(II) was titrated in 0.01 M HCl to a biamperometric end-point with gold-plated platinum wire indicating electrodes polarized at 100 mV. Recoveries were 100.7± 1.8% (0.7 mg) and 100.4 ± 2.3% (0.4 mg). This new system allows titrations over a wide range of acidities and oxidation potentials.     

Simultaneous Potentiostatic Coulometric Determination of Platinum and Palladium

Based on a voltammetric study of the electrochemical behavior of Pt(IV) and Pd(II) in a 1 M HCl + 0.1 M ethylenediamine hydrochloride solution at a carbon–graphite electrode, we have found the optimum conditions for the simultaneous determination of 0.2 to 3 mg of platinum and palladium with a relative standard deviation of less than 0.5%.The oxidation reactions were Pd(0) Pd(II) and Pt(II) Pt(IV). Mass excesses of analytes of 3.5- to 4.5-fold with respect to each other did not interfere with the determination of individual elements. With alternate cathodic and anodic polarization of the electrode, these elements can be multiply determined in a single portion of solution. The procedure was used for the simultaneous determination of platinum and palladium in process solutions of KP-1 platinum concentrate after the separation of gold and silver and also in platinum- and palladium-based alloys.     

Solvent extraction separation of tin (IV) with 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (PC-88A)

Solvent extraction of tin(IV) from hydrochloric acid media was carried out with 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (PC-88A) in toluene. Tin(IV) was quantitatively extracted with 2.5x10(-2) M PC-88A in toluene from 0.1-0.3 M HCl when equilibrated for 5 min. Tin(IV) from the organic phase was stripped with 4 M HCl and determined spectrophotometrically by both the morin and pyrocatechol violet method. The nature of the extracted species was determined from the log-log plots. Various other diluents such as xylene, hexane and cyclohexane also gave quantitative extraction of tin. The metal loading capacity of the reagent was found to be 0-15 ppm of tin(IV). The extraction of tin(IV) was carried out in the presence of various ions to ascertain the tolerance limit of individual ions. Tin(IV) was successfully separated from commonly associated metal ions such as antimony(III), bismuth(III), lead(II), thallium(I), copper(II), nickel(II), etc. The method was extended for determination of tin in real samples.     

Investigation of redox properties of different PtSn/Al2O3 catalysts.

Alumina-supported Sn and PtSn particles are studied by 119Sn M?ssbauer spectroscopy after oxidation and reduction under various conditions. The observed species of Sn(IV), Sn(II) and Sn(0) are grouped in several categories, each being characterised by distinct structural properties. Tin phases in contact with the support or with platinum are identified. The results are used to establish a model describing the phase transformations occurring in PtSn particles under oxidising or reducing conditions. Particular attention is paid to the reduction/reoxidation mechanisms governing H2/O2 double titrations. An increased reactivity of tin towards oxygen, induced by the contact with platinum, is demonstrated. It is shown that tin contributes to the oxygen uptake VO1 of a first titration cycle by platinum-catalysed transformation of Sn(II) into an oxometallic phase Pt(x)Sn(O). The oxygen titre VO2 of a second cycle is due to O2 chemisorption on platinum only.     

Electrochemical investigations of cationictrans-haloarylisocyanidebis(tertiaryphosphino)platinum (II) complexes

Summary The electrochemical behaviour of a series of cationic platinum(II) isocyanide complexes has been studied in acetonitrile. All the tested compounds are oxidized at a platinum electrode via a two-electron process and reduced at a platinum or mercury electrode via two successive one-electron steps. The anodic step involves the formation of platinum(IV) complexes. The main reduction product formed in correspondence to the first cathodic process is a stable dimer platinum(I) containing bridging isocyanide ligands. Platinum(0) species are formed in the subsequent reduction step.     

Voltammetric behavior of the iron(II)-(III) and cerium(III)-(IV) couples in potentiometric titrations at constant current and amperometric titrations with two indicator electrodes

The voltammetric behavior at the rotated platinum electrode of the iron(II)-(lII) and cerium (III)-(IV) couples in sulfuric and hydrochloric acids has been investigated The iron and cerium couples are not reversible at a platinum electrode when current flows in the system, and the current-potential curves deviate considerably from those predicted on the basis of reversibility Titration curves for potentiometric titrations at constant current using one and two indicator electrodes are predicted from the current-potential curves and compared with the experimental curves.The degree of reversibility of the iron couple depends greatly on the pretreatment of the electrode The current-potential curves of the iron couple at a platinum electrode coated with a monomolecular film of platinum oxide approach reversibility while those at a clean electrode are highly irreversible Experimental and calculated titration lines for amperometric titrations using two indicator electrodes are compared, and the effects of medium and applied e.m.f. upon the characteristics of the titration curves are considered.     

Redox transformations of bis(2,2'-bipyridine)(1-methyl-1-pyridin-2-yl-ethylamine)ruthenium(II)

The amineruthenium(II) complex Ru(bpy)2(mpea)2+ has been prepared by the direct reaction of 1-methyl-1-pyridin-2-yl-ethylamine (mpea) with Ru(bpy)2Cl2 in ethanol/water and isolated as the hexafluorophosphate salt. Electrochemical analysis of this complex shows that it undergoes sequential one-electron oxidations to an amidoruthenium(III) intermediate (E degrees' = 1.086 V vs NHE) and then to an amidoruthenium(IV) (E degrees' = 0.928 V) or imidoruthenium(IV) (E degrees' = 1.083 V) complex, depending upon the solution pH (pKa = 2.62 for the amidoruthenium(IV) species). At higher potentials ( Epa = 1.5 V in 1.0 M H2SO4), the amido- or imidoruthenium(IV) species is irreversibly oxidized to the corresponding nitrosoruthenium(II) complex. The mechanism for this transformation appears, on the basis of b3lyp/cpcm/cep-31g(d) computations, to proceed through an imidoruthenium(V) intermediate, which is rapidly attacked by water to yield a Ru(II)-bound hydroxylamine radical, which is readily oxidized and deprotonated to produce the nitrosoruthenium(II) complex. The nitrosoruthenium(II) complex is quantitatively reduced to the original [Ru(bpy)2(mpea)]2+ complex at relatively negative potentials ( Epc = -0.2 V in 1.0 M H2SO4).     

Flow-Injection Study and Analytical Applications of the Reactions of Palladium(II) and Platinum(IV) with Tin(II) Chloride in Hydrochloric Acid Solutions

The interaction of palladium(II) and platinum(II) with tin(II) chloride in hydrochloric acid solutions was studied by flow-injection (FI) spectrophotometry. It was found using kinetic measurements in the stopped flow mode that the composition of detected products and the rate of their formation depend on the concentrations of tin(II) and chloride ions in the reaction zone and on the acidity of the solution. Optimal FI conditions were found, and the selectivity of interaction of palladium(II) with tin(II) chloride was estimated for the detection of the signal at 407 nm (yellow form) and 646 nm (green form). It was demonstrated that the reaction of the formation of yellow platinum(IV) complexes is slower than that for palladium(II), especially at rather low concentrations of hydrochloric acid in the reaction flow. Based on the detection of green complexes of palladium(II) with tin(II) chloride, a flow injection method was proposed for the selective spectrophotometric determination of palladium(II) in the presence of other platinum-group metals. The height of the recorded peak is directly proportional to the concentration of palladium(II) in the injected solution in the range of 0.028–0.300 mM. The method was used for the analysis of pharmaceuticals and industrial catalysts.     

Determination of Selenium(IV) by Stripping Voltammetry at a Mercury-Film Electrode

A procedure was proposed for the determination of selenium(IV) by stripping voltammetry on a mercury-film electrode at an electrolysis potential of +0.4 V versus the saturated silver–silver chloride reference electrode in a 1 M H₂SO₄ solution. The current of the cathodic peak is a linear function of the selenium(IV) concentration in the range from 5 × 10^–3 to 3 × 10^–1 mg/L (6.3 × 10^–8 to 3.8 × 10^–6 M) at a time of electrolysis of 30 s (t _el). The detection limit for selenium is 1 × 10^–4 mg/L (1.3 × 10^–9 M) at t _el = 300 s. It was shown that selenium(IV) can be determined in the presence of 10 mg/L Zn(II), 1 mg/L Cd(II), 0.5 mg/L Pb(II), and 0.2 mg/L Cu(II). A procedure for the determination of selenium in natural, mineral, and potable water was proposed.     

Electron Transfer Studies of TIN(IV)/TIN(II) in Acid Media

Abstract

Cyclic voltammaetry of mixed tin(II)/tin(IV) solutions was investigated in 6M HCl on gold and mercury electrodes. It was found that the reduction of tin(II) to tin(iv) proceeded irreversibly while tin(II) to tin(IV) was reversible. Two forms of tin(IV) are postulated. The peak potential for the reduction of tin(IV) was a function of both tin(II) and tin(IV) while that for the oxidation of tin(II) was a function only of tin(II) concentration Potentials for all oxidations and reductions were a function of potential scan rate.     

The effect of tin(II) chloride on the liquid-liquid extraction of tetrachloroplatinate(II) ions by triphenylphosphine in dichloromethane

The effect of tin(II) chloride on the extraction of tetrachloroplatinate(II) in 1.0–1.5 M HCl into dichloromethane with triphenylphosphine (TPP) is described. Tin(II) chloride dramatically increases the rate and efficiency of platinum extraction. The percentage of platinum extracted depends in a complicated way on the time allowed for extraction, the Pt:Sn(II) ratio, the Pt:TPP ratio, and to a lesser extent to the hydrochloric acid concentration. Tin is initially extracted into the organic phase, probably as [Pt(SnCl₃)Cl(PPh₃)₂], but is subsequently back-extracted into the aqueous phase, as a result of the relatively slow disproportionation reaction: [Pt(SnCl₃)Cl(PPh₃)₂]_org + cl^? ? [Pt(PPh₃)₂Cl₂]_org + SnCl^?₃.     

V(IV)在不同电极上氧化还原动力学研究

分别以导电塑料集流板、石墨棒、铂片作工作电极,应用循环伏安法和稳态极化法研究V(IV)的阳极氧化动力学过程,计算V(IV)在不同材料电极上的反应动力学参数.结果表明,以导电塑料板作电极,硫酸氧钒有较宽的水稳定区,且析氧电位较高;在石墨电极上,V(V)/V(IV)的交换电流密度较大,表现出较好的可逆性;而在铂电极上,硫酸氧钒更易析氢.