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.     

Spectrophotometric determination of nickel(II), palladium(II) and copper(II) in presence of each other and other ions with 1-(o-carboxyphenyl)-3-hydroxy-3-phenyltriazene

Summary 1-(o-Carboxyphenyl)-3-hydroxy-3-phenyltriazene was found to be an excellent spectrophotometric reagent for the determination of nickel(II), palladium(II) and copper(II). At pH 6.8–8.3, 2.4–3.5 and 2.2–3.8, nickel, palladium and copper form greenish yellow, yellowish orange and light green complexes with maximum absorption at 410, 410, 400 nm, respectively. The systems obey Beer's law with optimum ranges from 0.25 to 2.0 ppm for Ni(II), 0.5–4.0 for Pd(II) and 0.5–4.0 for Cu(II); the elements form 11 complexes with the instability constants 2.1×10^–5, 1.5×10^–5 and 2.0×10^–5, resepctively. Effects of other anions and cations on the colour systems have been studied and procedures for the determination of Ni(II), Pd(II) and Cu(II) in presence of each other are described.

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Spektrophotometrische Bestimmung von Nickel(II), Palladium(II) und Kupfer(II) nebeneinander und in Gegenwart anderer Ionen mit Hilfe von 1-(o-Carboxyphenyl)-3-hydroxy-3-phenyltriazen

Zusammenfassung Ni, Pd und Cu bilden mit dem Reagens bei pH 6,8–8,3, 2,4–3,5 bzw. 2,2–3,8 grünlich-gelbe, gelblich-orange bzw. hellgrüne Komplexe mit Absorptionsmaxima bei 410, 410 bzw. 400 nm. Das Beersche Gesetz wird in den Bereichen 0,25–2,0, 0,5–4,0 bzw. 0,5–4,0 ppm befolgt. Die Elemente bilden 11-Komplexe mit den Instabilitätskonstanten 2,1 · 10^–5, 1,5 · 10^–5 bzw. 2,0 · 10^–5. Der Einfluß anderer Kationen und Anionen wurde untersucht und Arbeitsvorschriften werden angegeben.

     

Use of Silica Gel Chemically Modified with Mercapto Groups for the Extraction, Preconcentration, and Spectroscopic Determination of Palladium

Silica gel chemically modified with mercaptopropyl groups is proposed for the extraction and preconcentration of palladium. This silica gel extracts palladium(II) at an acidity from 6M HCl to pH 4 with distribution ratios at a level of n× 10⁴ g/cm³. Hyphenated procedures for the adsorption–photometric determination of palladium with detection limits of 0.1 g/0.1 g of the adsorbent have been developed. The procedure includes the adsorption preconcentration of palladium, elution by hot (50 ± 5°C) 8% thiourea in 1M HCl, and atomic absorption determination of palladium in the eluate (detection limit is 0.05 g/mL). The procedures were applied to the determination of palladium in standard reference samples of copper–nickel ore and copper concentrate.     

Extractive photometric determination of palladium with o-mercaptobenzoic acid

A procedure is described for the extractive photometric determination of palladium(II) with o-mercaptobenzoic acid. The reagent forms a yellow complex having maximum absorption at 365–370 mμ. The complex is quantitatively extractable with chloroform in the presence of pyridine at pH 5.2–7.2. The color develops immediately at room temperature and is very stable. Beer's law conforms over the range of 0.37–5.86 ppm of palladium. Most of the cations do not interfere in the presence of ascorbic acid and EDTA. Gold and silver are effectively masked with excess of thiocyanate prior to the addition of ascorbic acid and EDTA. Many common anions do not interfere. The molar absorptivity and Sandell sensitivity are 16.7 × 10³ and 0.0065 μg/cm². The reagent forms a 2:1 complex with palladium. The proposed method is simple, rapid, and selective for the determination of palladium(II).     

Application of Thermal-Lens Spectrometry to a Study of the Interaction of Trace Nickel(II) with Dimethylglyoxime

Thermal-lens spectrometry was applied to a study of the properties of a nickel(II) complex with dimethylglyoxime at a concentration level of n × 10^–8–n × 10^–6 mol/L. The possibility of determining the solubility of the complex and the characteristics of its adsorption on the glass surface of laboratory ware was demonstrated. The stability constants of the complex in water–ethanol mixtures (9 : 1) were determined. The found data made it possible to optimize the conditions for the photometric determination of nanomolar concentrations of nickel. The optimized procedure was used for a thermal-lens determination of nickel(II) traces in heteropoly compounds and high-purity water.     

Flow Analysis of Transition Metals by Thermal Lensing

The conditions for the flow determination of Al(III), Bi(III), Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Mn(II), Nd(III), Ni(II), Pb(II), Pr(III), and Zn(II) by reaction with Xylenol Orange in aqueous solutions at pH 4.5 and the determination of Cd(II), Co(II), Cu(II), Fe(II), Ni(II), Pb(II), and Zn(II) by reaction with 4-(2-thiazolylazo)resorcinol in water–ethanol mixtures (5 : 1) at pH 5.0 using an injected sample volume of 80 L were proposed. The limits of detection were n × 10^–8–n × 10^–7 mol/L; the linearity ranges in the calibration graphs were of about three orders of magnitude; the relative standard deviation was of 3–7%.     

Oscillopolarography of Palladium(II)–Tropeolin 0 Complexes

The electrochemical behavior of palladium(II) complexes of Tropeolin 0 (Tr0) was studied by linear-potential-sweep voltammetry in acetate–ammonia buffer solutions. The optimum conditions for determining palladium(II) with Tr0 were found. The composition of the complex was found to be Pd : Tr0 = 1 : 2. A procedure was proposed for determining palladium(II) with a detection limit of 2.54 × 10^–7M. The procedure was used for determining palladium(II) in capacitors.     

2-(5-Nitro-2-Pyridylazo)-5-(N-Propyl-N-Sulfopropylamino)Phenol as a new analytical reagent for flow-injection spectrophotometric determination of trace vanadium(V)

A flow injection method using 2-(5-nitro-2-pyridylazo)-5-(N-propyl-N-sulfopropylamino)phenol-(Nitro-PAPS) as a new chromogenic reagent is presented for sensitive and rapid determination of vanadium. Nitro-PAPS reacts with vanadium(V) in weakly acidic medium to form a water soluble complex of molar absorptivity of 8.0 × 10⁴L mol^–1 cm^–1 at 592 nm (maximum absorption wavelength), which permits the straightforward application of a flow injection system to the sensitive determination of vanadium. Under the optimum conditions established, a linear calibration graph was obtained in the range 1–120 ng mL^–1. The relative standard deviation for 60 ng mL^–1 vanadium was 2.2% (n = 5) and the limit of detection was 1 ng mL^–1. The sample throughput is about 40 h^–1. Most inorganic and organic anions examined did not interfere even at concentrations of 3000–6000 times of vanadium. Interference from cobalt(II), copper(II) and nickel(II) at 200ng mL^–1 levels can be overcome by the addition of N-(dithio-carboxy)sarcosine. The recoveries for each 20 and 10 ng mL^–1 vanadium added to the river water were 98 and 97%, respectively.The authors express their thanks to Miss Miho Suzuki and Miss Hiroyo Yamada for their experimental assistance in part.     

Selective Extraction–Spectrophotometric Determination of Traces of Palladium in Catalysts

The simple, sensitive, and highly selective determination of palladium is based on the reaction between Pd(II) and 1,2-bis[methyl(2-aminocyclopentene carbodithioate)] ethane and extraction of the complex into dichloromethane. Beer's law is obeyed in the concentration range 0.19–10 μg ml⁻¹Pd. Relative standard deviations were 0.7–1.1%. The procedure has been successfully applied to the determination of palladium in different samples of catalysts.     

A new procedure for the spectrophotometric determination of nitrogen(II) oxide in solutions

A new simple and reliable procedure was developed for the spectrophotometric determination of nitrogen(II) oxide. The procedure is based on the determination of excess oxygen after its reaction with NO. Alkaline solutions of thiourea dioxide were used for the determination of oxygen. It was found that the decomposition of an alkaline solution of thiourea dioxide under aerobic conditions is accompanied by the formation of dithionite, and its concentration is proportional to the concentration of oxygen in the solution. The absorbance of the resulting dithionite was measured at 315 nm. The solutions obeyed Beers law at oxygen concentrations of 1 × 10^–5–1.5 × 10^–3 M. The analytical range for NO was 1 × 10^–5–1.5 × 10^–3 M. The proposed procedure was also used for the determination of nitrogen(II) oxide in aqueous-ethanolic solutions.Translated from Zhurnal Analiticheskoi Khimii, Vol. 60, No. 1, 2005, pp. 27–29.Original Russian Text Copyright © 2005 by Pukhovskaya, Guseva, Makarov, Naidenko.     

A sensitive and highly selective extractive spectrophotometric method for the determination of palladium

Summary A Sensitive and Highly Selective Extractive Spectrophotometric Method for the Determination of Palladium Palladium forms an anionic chelate with 4-(2-pyridylazo)resorcinol (PAR, H₂R) which is extractable with xylometazolonium cation (XMH) into chloroform in the pH range 7.2–7.8 giving an intensely pinkish red coloured solution. The coloured species exhibits maximum absorbance at 520 nm with molar absorptivity 3.34×10⁴1·mole^–1·cm^–1 and obeys Beer's law in the range 0.8–5.30g/ml of palladium. The composition of the extracting species is found to be 111 for Pd(II)PARXMH. Large concentrations of EDTA and oxalate have no interference in the spectrophotometric determination of palladium by this procedure. Based on this a highly selective and sensitive method for the determination of palladium in the presence of Zn(II), Cd(II), Hg(II), Fe(III), Mn(II), Co(III), Mo(VI), Ru(IV), Sb(III), Al(III) is described. The application of this method for the determination of palladium in synthetic mixtures corresponding to the composition of jewel alloy and stibiopalladinite mineral is also demonstrated.     

Spectrophotometric determination of iron after separation of its 9,10-phenanthrenequinone monoximate on microcrystalline naphthalene

A sensitive and selective spectrophotometric method has been developed for the determination of iron as Fe(II) or Fe(III) using 9,10-phenanthrenequinone monoxime (PQM) as the complexing agent. Fe(II) and Fe(III) react with PQM to form coloured water insoluble complexes which can be adsorbed on microcrystalline naphthalene in the pH ranges 3.7–6.2 and 2.0–8.4, respectively. The solid mass consisting of the metal complex and naphthalene is dissolved in DMF and the metal determined spectrophotometrically by measuring the absorbances Fe(II) at 745 nm and Fe(III) at 425 nm. Beer's law is obeyed over the concentration range 0.5–20.0 g of iron(II) and 20–170.0 g of Fe(III) in 10 ml of DMF solution. The molar absorptivities are 1.333 × 10⁴ 1 · mole^–1 · cm^–1 for Fe(II) and 2.428 × 10³1· mole^–1 · cm^–1 for Fe(III). The precision of determination is better than 1%. The interference of various ions has been studied and the method has been employed for the determination of iron in various standard reference alloys, bears, wines, ferrous gluconate, human hair and environmental samples.     

Polarographic and voltammetric determination of trace amounts of 2-nitronaphthalene

The polarographic behaviour of 2-nitronaphthalene was investigated by DC tast polarography (DCTP) and differential pulse polarography (DPP), both at a dropping mercury electrode, and differential pulse voltammetry and adsorptive stripping voltammetry, both at a hanging mercury drop electrode. Optimum conditions have been found for the determination of 2-nitronaphthalene by the given methods in the concentration ranges of 2×10^–6–1×10^–4, 2×10^–7–1×10^–4, 1×10^–8–1×10^–4 and 2×10^–9–1×10^–8 M, respectively. Practical applicability of these techniques was demonstrated by the determination of 2-nitronaphthalene in drinking and river water after its preliminary separation and preconcentration using liquid–liquid and solid-phase extraction with limits of determination of 3×10^–10 M (drinking water) and 3×10^–9 M (river water).     

A Chemometric Approach to the Indirect Potentiometric Determination of the Components of a Redox Couple

A chemometric approach to the determination of the components of a redox couple without their preseparation was proposed. The approach is based on the transformation of a potentiometric curve obtained by the multiple addition method to a direct regression line with a cotangent numerically equal to the analyte concentration. The approach was tested on simulated and experimental data for the reversible Fe(III)–Fe(II) system and applied to the determination of Cr(VI) in model solutions using excess solution of the Mohr's salt as an auxiliary reducing agent. In real determinations of Fe(III, II) and Cr(VI) in concentration ranges from 1 × 10^–3to n× 10^–5and from 2 × 10^–3to 5 × 10^–4M, RSD varied from 0.2 to 8% and from 3 to 12%, respectively.     

Solvent Extraction–Photometric Determination of Palladium Using Complexation with 1-(2-Pyridylazo)-2-Naphthol

Palladium(II) complexation with 1-(2-pyridylazo)-2-naphthol (PAN) in aqueous solutions followed by extraction with chloroform and photometric detection was studied. The best conditions were found for the formation of the complex in an aqueous solution and for its extraction with chloroform that provided a sufficient degree of binding palladium ions. The stability constant of the complex cation PdX⁺, which is extracted by chloroform as an ion pair [PdX]⁺[An^–] (An^–– CH₃COO^–), was calculated using the methods proposed by Rossotti (log K _stab= 18.73) and Komar' (log K _stab= 18.82). The equilibrium constant of the complexation reaction was also calculated (5.45 × 10⁴). It was shown that components of nonferrous alloys affect the determination of palladium by photometry as its complex or ion pair with PAN in chloroform.     

4(5)-D-Arabinotetrahydroxybutylimidazoline-2-thione (THBIT), a new reagent for the spectrophotometric determination of palladium

Summary 4(5)-D-Arabinotetrahydroxybutylimidazoline-2-thione, THBIT, is proposed as a new reagent for the spectrophotometric determination of Pd(II). Pd(II) forms 11, 12 and 14 complexes with THBIT. The system conforms to Beer's law up to 5g/ml palladium concentration in aqueous medium (molar absorptivity, 1.99×10⁴ l· mole^–1·cm^–1 at 338 nm). The most serious interference is from Hg(II), Os(VIII), Ru(IV), Cr(VI), V(V) and S₂O₃ ^2–. The method has been used successfully for the determination of palladium in catalysts and synthetic samples.     

Effect of using mixed ion-pairs on PVC-membrane electrodes for ephedrine

Mixed ion-pairs based on the use of ephedrinium (EPH)-TPB plus EPH-reineckate (II) and phenylephrine-TPB plus EPH-reineckate (III) were tried for use in plastic membranes. The results were compared to those of an EPH-reineckate (I) single ion-pair electrode. The Nernstian slopes were 50, 49 and 55 mV decade^–1 for membranes I, II and III, respectively. The linear concentration ranges were 10^–5–10^–1, 4.0 × 10^–5–10^–1 and 6.3 ×^–5–10^–1 M ephedrine. The detection limits were 4 ×^–6,10^–5 and 1.2 × 10^–5 M ephedrine for membranes I, II and III, respectively. The pH ranges were 4–9, 3–9 and 2–8 for I, II and III-membranes, respectively. Selectivity coefficient values for membrane II were better than those for membranes I and III. The effects of increasing KC1 concentration and temperature changes were explained for the three electrodes. The isothermal temperature coefficients were 0.00145, 0.0007 and 0.00055 V/ °C for electrodes I, II and III. Electrode III was applied for the determination of ephedrine in its pharmeaceutical preparations with an overall relative standard deviation range of 1.3–2.4% and an overall mean recovery value of 98.1%.     

Spectrophotometric and derivative spectrophotometric determination of palladium(II) using pyridopyridazine dithione in the presence of non-ionic surfactant

Pyridopyridazine dithione (PPD) was synthesized as a new sensitive and selective reagent for spectrophotometric and derivative spectrophotometric determination of palladium(II). In aqueous and micellar medium, PPD forms 1:4 complexes having molar absorptivities of 4.68 × 10⁴ and 5.74 × 10⁴lmol^–1 cm^–1 at 570 and 615 nm, respectively. Beer's law was obeyed up to 2.2 and 2.5 g ml^–1 with detection limits of 0.2 and 0.1g ml^–1. The relative standard deviations for 1.23g ml^–1 were 2.6 and 1.3%, in the absence and presence of Triton X-100. In fourth-derivative mode, the regression equation, linear range, detection limit and RSD for 0.075 g ml^–1 wereD ₄ = 4.3C + 1.5 × 10^–3, 0.013 – 0.23 g ml^–1, 3.7 ng ml–1 and 0.78%, respectively. The ionization constants of the reagent and stability constants of the complexes were evaluated. The method is free from interference by most common metal ions and anions. The method was applied for determination of palladium in activated charcoal.     

A kinetic method for the determination of zinc(II) in presence of a large excess of cadmium(II) by the different dissociation rate of their complexes with 5,10,15,20-tetrakis(4-sulfonatophenyl)porphine

Summary Acid-dissociation reaction of the cadmium(II) complex of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphme (H₂tspp) proceeds about 10¹² times as fast as that of the zinc(II) complex. This provides the basis for a kinetic determination of zinc(II) in presence of a large excess of cadmium (II). The absorbance at soret-band (421 nm) of Zn(II)(tspp) was used to monitor the reaction. At 5.0×10^–2 M hydrogen ion concentration, Cd(II)(tspp) dissociates completely to Cd²⁺ in 1 s and only the reaction associated with Zn(II)(tspp) is observed during the reaction time from 30 s to 5 min. Zinc(II) concentration <10^–6 M is determined in the presence of 10^–2 M cadmium(II). The molar absorption coefficient is 2.7×10⁵ M ^–1 cm^–1. Iron(III), aluminum(III) and cobalt(II) being masked sodium tartrate, this method is highly selective and is free from interferences of most substances usually encountered. The method was applied to determine zinc(II) in tap water and in cadmium(II) sulfate.     

Investigations of Cobalt, Nickel, and Copper Diethyldithiocarbamates Using Thermal Lens Spectrometry

Thermal lens spectrometry was used to study the dissociation kinetics of diethyldithiocarbamate complexes of copper(II), cobalt(III), and nickel(II) as a function of pH in the presence of chloride and sulfate ions. It is shown that, as distinct from conventional spectrophotometric and potentiometric measurements, the reversible dissociation of the test complexes and the irreversible oxidation of the ligand can be studied separately (at a level of n × 10^–8–n × 10^–6 M) using thermal lens spectrometry. Because of work in more dilute solutions and due account of the kinetic features of the systems in question, thermal lens spectrometry provides a higher accuracy of the determination of stability constants for diethyldithiocarbamate complexes of copper(II), cobalt(III), and nickel(II). The adsorption of the diethyldithiocarbamate complexes in question from water–ethanol solutions (1 : 3) on Silasorb C₁₈ silica is studied, and the adsorption constants are determined. The limits of detection of copper(II), cobalt(III), and nickel(II) diethyldithiocarbamates obtained in extraction–thermal-lens determination are n × 10^–8 M.