The polarographic determination of isopropenyl esters in aqueous solution

Both mercuration and bromination have been used for the polarographic analysis of isopropenyl esters in aqueous solutions. For mercuration, no disadvantages were found in comparison with the established methods [4,5] for the estimation of vinyl esters in methanol, due to either the lower rate of mercuration [5,22] or the expected lower stability of the depolariser formed in aqueous solution, the hemiacetal mercuric acetate addition product. At concentrations below 10^?2 mol l^?1, acetone did not interfere [38] with the determinations.     

Differential pulse polarographic determination of orthophosphate in aqueous media

The determination of orthophosphate in aqueous media by differential pulse polarography is described. It is based on determination of the molybdenum in 12-phosphomolybdic acid. High sensitivity is achieved by measuring the polarographic wave due to the catalytic reduction of perchlorate or nitrate in the presence of molybdenum(VI). The method is suitable for samples as small as 3.5 ml which contain as little as 9 ng of phosphorus per ml. The average relative deviation is 3.0% at the 0.045 mg/l. phosphorus level and 1.6% at the 1.2 mg/l. level. Results for the analysis of EPA quality-control water and real surface-water samples are reported.     

Sine-wave polarographic determination of zirconium or niobium in aqueous media

The sine-wave polarographic determination of zirconium in aqueous media was investigated using solutions which were 0.55 – 5.5·10^-3M in zirconyl chloride and 1 M in potassium chloride and had been adjusted to pH 2.0 with hydrochloric acid. It was possible to determine zirconium in the concentration range of 0.05 to 0.4 mg per ml. The sine-wave polarographic behavior of zirconium in aqueous solutions in the pH range 2–3 is discussed. The sine-wave polarographic determination of niobium in aqueous media was investigated using concentrated sulfuric acid containing 5 to 0.1 mg of niobium per ml in a supporting electrolyte of citric acid; the determination of niobium was possible down to 0.1 mg of niobium per ml of concentrated sulfuric acid although the D.C. polarographic method was impractical for the determination of less than 0.5 mg of niobium per ml.     

Applications of gamma-spectrometry in determining chlorine in aqueous solutions

A method is described for the radioanalytical determination of traces of chlorine in aqueous solutions without radiochemical separation or purification. Using a gamma-spectrometer with monocrystal scintillator, the sensitivity of the analysis is about 1·10⁻⁸ g of chlorine/ml, the time of analysis being 15 minutes. For the selective determination of chlorine in aqueous solutions containing a large amount of impurities, a bicrystal scintillation sum-coincidence spectrometer was employed with 120×100 mm NaI(Tl) crystals and thus the³⁸Cl cascade radiation could be used. Application of the sum-coincidence spectrometer allowed a reliable determination of 1·10⁻⁷ g of Cl/ml against a background of 1·10⁻⁵ g of Na/ml.     

A new water-soluble chromogenic indicator: an application to the determination of chlorine in aqueous solutions.

A novel compound, N,N'-bis(2,4-di-sulfobenzyl)tolidine tetrasodium salt (SBT), was synthesized for use as a chromogenic indicator for oxidizing substances, and its applicability to the colorimetric determination of chlorine in water was examined.     

Voltammetric determination of the chlorine content of aqueous solutions, using a silicone-rubber based graphite electrode

A method for the determination of chlorine and hypochlorous acid in 0.1N sulphuric acid by voltammetry is described. The method may be applied to stirred and flowing solutions and has a possible use in the monitoring of sewage effluent systems.     

Electroinjection determination of aluminum in aqueous solutions

A procedure is proposed for determining aluminum(III) in water over a concentration range of 0.1–2.0 mg/L in the presence of commensurable amounts of iron(III) using electroinjection analysis. The following parameters were varied in the experiments: the composition and pH of a working buffer solution, the reagent-to-metal concentration ratio, the time of sample injection, the composition of a buffer solution in sample preparation for analysis, the concentration of the reagent (Xylenol Orange), and the reaction time. As a result of this, the sensitivity and selectivity of determining aluminum were improved as compared with the currently available procedures.     

The chemical passivation of copper in ammonia solutions containing chlorine ions

It was shown that the CuCl layers deposited on copper chemically and electrochemically from copper-ammonia solutions were different. The layer formed chemically was loose, and that formed on the anode, dense. During multilayer copper passivation, the chemically deposited CuCl layer interfered with the formation of electrochemical CuCl and Cu₂O layers.     

Calorimetric determination of activated carbons in aqueous solutions

The interactions among five samples of activated carbons, obtained from different lignocellulosic materials with different degrees of activation of approximately 20% and aqueous solutions of phenol and 4-nitro phenol are studied by means of the determination of immersion enthalpies. It is established that the obtained activated carbons are of a basic character and show values for the pH at the point of zero charge, pH_PZC, that range from 7.4 to 9.7 and, in all cases, higher total basicity contents than the values obtained for total acidity. The immersion heat of the activated carbons in CCl₄ and water is determined obtaining values which are higher for CCl₄ immersion and vary from 31.4 to 48.6 J g⁻¹. The hydrophobic factor, hf, it is calculated from the relation between of the immersion heat of the activated carbons in CCl₄ and the immersion heat in water, the obtained values were 2.98 and 6.75, which are greater than 1 due to the greater values obtained in CCl₄ when compared to the values obtained in water. Immersion enthalpies in phenol solution range from 7.6 to 13.9 J g⁻¹ and for the case of 4-nitro phenol such enthalpies range from 12.7 to 20.5 J g⁻¹; all the 5 samples studied showed a higher value for the heat of immersion in aqueous solutions of 4-nitro phenol.     

Photoelectrochemical determination of inorganic mercury in aqueous solutions

An analytical method using an optical probe in a photoelectrochemical cell for the sensitive and selective determination of aqueous Hg²⁺ is presented. A previously synthesized Hg²⁺ selective chemosensor, proven to be Hg²⁺ sensitive up to 2 μg L⁻¹, has been immobilized onto indium tin oxide (ITO) electrodes in a composite form with polyaniline. The coated ITO electrode was placed in a photoelectrochemical cell under closed circuit conditions in which the optical recognition of the chemosensor was converted to a measurable signal. A composite of the fluorescent chemosensor, Rhodamine 6G derivative (RS), and polyaniline (PANI) was immobilized on ITO glass plates and subjected to photovoltage measurements in the absence and presence of Hg²⁺. The optical responses of the coated electrode were used to determine the sensitivity and selectivity of the immobilized sensor to Hg²⁺ in the presence of background ions. The optical response of the PANI-dye coated electrode increased linearly with increasing Hg²⁺ concentration in the range 10-150 μg L⁻¹, with a detection limit of 6 μg L⁻¹.     

Photometric cyclic-injection determination of arsenic in aqueous solutions

A procedure for the photometric on-line determination of trace arsenic in aqueous solutions was developed. The procedure is based on the reaction gas extraction of arsenic as arsine followed by liquid-absorption separation from a gas phase into a solution of a photometric reagent (2-(p-nitrophenyl)-3,5-diphenyltetrazolium chloride). The determination limit was 10 μg/L at a sample volume of 50 mL.     

Micellization in aqueous solutions of mixed surfactants containing alkylpolyglucosides

Tensometry is used to find the dependences of critical micelle concentration in aqueous solutions on the composition of mixed systems comprising anionic surfactants (alkyl sulfates and individual sodium soaps) and alkylpolyglucosides. Mixed micellization is revealed and the compositions of micelles and the parameters of intermolecular interaction are calculated. The average hydrodynamic diameter of micelles is measured by dynamic light scattering.     

Radiochemical oxidation of hydrazine in aqueous solutions containing oxygen

The chain mechanism of oxidation of hydrazine in aqueous solutions saturated with oxygen at pH > 7.5 was established. The yields of radiochemical decomposition of hydrazine increase with a decrease in the absorbed dose rate, an increase in the concentration of hydrazine, and the pH of the solution and attains hundreds of molecules per 100 eV of absorbed energy. It is hypothesized that the chain process includes a stage of formation of the N₂H₃ radical, its reaction with O₂, and the formation of O₂ ^– or N₂H₃O₂. The chain propagation reaction is due to the reaction of molecules of N₂H₄ with N₂H₃O₂ or O₂ ^–.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2450–2453, November, 1989.     

Sulphur dioxide oxidation in aqueous solutions containing metal cations

Effect of vanadium cations as model inhibitors on SO₂ oxidation with air in iron sulfate solutions at 298–308 K has been studied and a mechanism of inhibition proposed.

---

V, , SO₂ 298–308 K. .

     

Extraction-chromatographic determination of sulfonated azo dyes in aqueous solutions

The extraction of sulfonated azo dyes E102, E110, E122, E124, and E129 from aqueous solutions using hydrophilic solvents and their mixtures in the presence of a salting-out agent (ammonium sulphate) has been studied. Some regularities of extraction have been revealed. The composition of the mobile phase has been optimized and a procedure has been proposed for the identification and determination of the dyes in aqueous solutions by thin-layer chromatography in concentrations of 0.1–0.01 μg/L. An office scanner and a personal computer have been used to process the results of the separate determination of the dyes.     

Radiation chemical oxidation of hydrazine in aqueous solutions containing oxygen

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, p. 1192, May, 1988.     

Indirect polarographic microdetermination of chlorine or bromine in organic compounds

A polarographic method for the microdetermination of chlorine or bromine in organic compounds is based on oxygen-flask combustion followed by an exchange reaction of chloride or bromide with excess of solid silver chromate, and polarographic determination of the chromate liberated. The method has been applied satisfactorily to a wide range of chlorine or bromine organic compounds with a coefficient of variation not exceeding 1%.