Indirect determination of vanadium by atomic absorption spectrometry

An indirect method for the determination of vanadium as vanadate by atomic absorption spectrometry is described. In neutral medium, vanadate forms a stable ion-association complex with copper (II) and biguanide, which is extractable into butanol with an efficiency higher than 99%. The copper content in the extract (and hence indirectly VO^?₃) is determined by aspirating it directly into an acetylene flame. The calibration graph is linear up to 3.4 μg ml^?1 of VO^?₃. The limit of detection is 16 ng ml^?1. Only chromium interferes.     

A spot test for the detection of periodate

Perrhenate is quantitatively extracted into methyl isobutyl ketone from aqueous solutions containing copper(II), azide and an excess of 2,2'-bipyridine. Measurement of the extracted copper either by spectrophotometry or by atomic absorption spectrometry, allows the determination of perrhenate in the ranges 16–40 μg ml⁻¹ or 3–16 μg ml⁻¹ in the final dilution, respectively. The procedure is highly selective, being applicable in the presence of a large concentration of molybdate and a considerable number of foreign ions. The extracted species corresponds to the formula CuN₃(bipy)₂ ReO₄.     

Fluorescent Complexes of Nucleic Acids/8-Hydroxyquinoline/Lanthanum(III) and the Fluorometry of Nucleic Acids

Abstract

The ternary fluorescent complexes of nucleic acids/8-hydroxyquinoline/ lanthanum (III) were studied. Nucleic acids in the study involve natured and thermally denatured calf thymus DNA, fish sperm DNA and yeast RNA. In the range of pH 8.0–8.4 (controlled by NH₃-NH₄Cl buffer) ternary fluorescent complexes are formed which emit at 485.0 nm for calf thymus DNA and at 480.0 nm for yeast RNA (when excited at 267.0 nm) and emits at 483.0 nm for fish sperm DNA when excited at 265.0 nm. Based on the fluorescence reactions sensitive fluorometric methods for nucleic acids were proposed. Using optimal conditions, the calibration curves were linear in the range of 0.4–3.6 μg˙ml^?1 for calf thymus DNA, 0.4–4.0 μg-ml^?1 for fish sperm DNA and 0.4–4.0 μg˙ml^?1 for yeast RNA, respectively. The limits of determination (3σ) were 0.076 μg˙ml^?1 for calf thymus DNA, 0.068 μg˙ml^?1 for fish sperm DNA and 0.329 μg˙ml^?1 for yeast RNA, respectively. Five synthetic samples were determined with satisfaction.

     

“Stat” methods in continuous flow analysis : Determination of Copper,Iron, Iodide and Hydrochloric Acid

A continuous flow “stat” method is described in which a certain arbitrarily imposed state in the flowing stream is automatically maintained by regulating the rate of flow of one of the components. The electronic system is regulated by measuring a physical phenomenon in the flowing solution. The method is illustrated by the examples of a continuous flow absorptiostat [Fe(III)/S₂O₃^2-/Cu(II)]for determinations of copper(II) (1–10 μg ml^-1), iron(III) (25–250 or 12.5–125 μg ml^-1), as well as for determination of iodide (12.8–128 μg ml^-1). A continuous flow conductostat [HCl/NaOH] for determination of 1–2.5 × 10^-4 M HCl is also described. This analytical technique is intended for automatic continuous monitoring of sample streams.     

Spectrophotometric determination of iron(III) with EDTA tetrahydrazide

The tetrahydrazide of ethylenediamine tetraacetic acid (NH₂NH)₄-EDTA was synthesized from the EDTA ester and hydrazine hydrate in ethanolic solution, the resulting (NH₂NH)₄-EDTA being recrystallized in 60% ethanol. When the spectrophotometric study of the iron(III) (NH₂NH)₄-EDTA complex in aqueous solution was made two absorption maxima at 530 and 450 nm at pH 4.5 and 11.0, respectively, were found. Beer's law is obeyed in the range 1.0–20.0 μg Fe(III) ml^?1 at 530 nm and pH 4.5 and 0.5–12.0 μg Fe(III) ml^?1 at 450 nm and pH 11.0, the molar absorptivities being 1.95 × 10³ 1 mol^?1 cm^?1 at 530 nm and 3.35 × 10³ 1 mol^?1 cm^?1 at 450 nm, respectively. The Ringbom optimal interval falls between about 3 and 18 μg Fe(III) ml^?1 at 530 nm and about 2–14 μg Fe(III) ml^?1 at 450 nm. The reaction between the metal and the ligand was also investigated. The method has been successfully applied to the determination of iron in talcs.     

Rapid spectrophotometric determination of ruthenium(III) with prochlorperazine maleate

A rapid, simple spectrophotometric method for the determination of μg amounts of ruthenium, based on the formation of a pink complex between the metal and prochlorperazine maleate (PCPM) in sulphuric or hydrochloric acid solution, is described. The complex has an absorption maximum at 530 nm and its molar absorptivity is 6.733·10³ l mol^?1 cm^?1. The sensitivity is 0.0151 μg Ru cm^?2 for log I_o/I = 0.001. Beer's law is valid over the range 0.2–10 μg Ru ml^?1 ; the optimal range for spectrophotometric determination is 0.8–8.0 μg Ru ml^?1. Job's method of continuous variation, the mole ratio method and the slope ratio method indicate a 1:1 composition for the complex. The effects of acidity, time, temperature, order of addition of reagents, reagent concentration, and the interferences from various ions are reported.     

Sequential spectrophotometric determination of rhodium and iridium with 1,5-diphenylcarbazide

Rhodium and iridium in mixtures are determined sequentially with 1,5-diphenylcarbazide at pH 5.0. The rhodium complex is formed at 70°C and is extracted into isobutanol for measurement. The iridium complex is then formed by heating for 45 min and measured in aqueous solution. Beer's law is obeyed over the ranges 0.56–2.8 μg ml^?1 for rhodium and 0.53–3 μg ml^?1 for iridium. Pt, Pd, Sn, Co, Ni and Cr can be tolerated in small amounts.     

Controlled anodic generation of the catalyst in kinetic continuous flow analysis

Controlled anodic dissolution of copper in a separate generator cell yields well-defined concentrations of catalyst, depending on the voltage applied. This adjustable generation of copper catalyst makes it possible to determine iron over a wide range of concentration (10–1500 μg Fe³⁺ ml^-1) via the iron(III)—thiosulphate reaction. By the copper(II)-catalyzed hydrogen peroxide—hydroquinone reaction, EDTA can be determined as an inhibitor (0.5–5 μg ml^-1) and cadmium(II) as a reactivator (1–10 μg ml^-1). As zinc(II) forms complexes with 2,2'-bipyridine, which activates copper in this reaction, it can be determined (5–50 μg Zn²⁺ ml^-1) by measuring the decrease in activation. The electrogeneration of silver ion as a catalyst is also described. The sulphanilic acid—peroxodisulphate reaction is catalyzed by silver(I), which is again activated by 2,2'-bipyridine. Zinc(II) can be determined (0.29–2.9 mg Zn²⁺ ml^-1) by the same principle as in the copper(II)-catalyzed reaction.     

Spectrophotometric determination of osmium with phthalimide dithiosemicarbazone by means of complex formation and catalytic reactions

Phthalimide dithiosemicarbazone forms a 1:1 complex with osmium at pH 3.3–4.5 (?₄₅₀ = 1.3 · 10⁴ l mol^?1 cm^?1 ) which is applied to the photometric determination of osmium; Beer's law is obeyed for the range 1–12 μg Os ml^?1. The oxidation of the reagent with cerium(IV) is catalyzed by osmium(VIII), and this reaction allows a more sensitive procedure for the determination of osmium; the calibration curve is linear over the range 0.05–0.4 μg Os ml^?1. The interferences in both procedures are described.     

Preconcentration of copper with the ion-pair of 1,10- phenanthroline and tetraphenylborate on naphthalene

A solid ion-pair material produced from 1,10-phenanthroline and tetraphenylborate on naphthalene provides a simple, rapid and fairly selective means of preconcentrating copper from up to 1000 ml of aqueous samples (about 200-fold concentration is possible). Copper is quantitatively adsorbed in the pH range 1.6–10.4 at a flow rate of 3 ml min^?1. The solid mass (0.2 g) is dissolved from the column with 5 ml of dimethylformamide (DMF) and copper is measured by atomic absorption spectrometry at 324.7 nm. Linear calibration is obtained for 2–28 μg of copper in 5 ml of DMF solution. Replicate determination of 14 μg of copper gave a mean absorbance of 0.220 (n = 7) with a relative standard deviation of 1.5%. The sensitivity for 1% absorption was 0.093 μg ml^?1. After optimization, the method was applied to determine trace copper in standard reference materials, natural waters, beverages and hair.     

The application of the ph-stat method to metal ion-catalyzed reactions

The pH-stat method, which is well known in organic chemistry and biochemistry, is used for the kinetic determination of metal ion catalysts. Indicator reactions that involve protons can be followed by controlled addition of standard base or acid. This is illustrated by the following examples: determination of copper(II) (0.03–0.3 μg ml^-1) with the indicator reaction ascorbic acid—peroxydisulphate; determination of molybdenum(VI) (0.2–2.5 μg ml^-1) with the indicator reaction thiosulphate—hydrogen peroxide; determination of zirconium(IV) (0.2–2 μg ml^-1) with the indicator reaction iodide—hydrogen peroxide; and determination of vanadium(V) (0.2–2 μg ml^-1) with the indicator reaction iodide—bromate. For one example, the copper—ascorbic acid—peroxydisulphate reaction, it is shown that the pH-stat method has distinct advantages over closed systems, giving considerably better sensitivity for the determination of copper (0.5–5 ng ml^-1 ).     

On-line preconcentration of trace copper for flame atomic absorption spectrometry using a spherical cellulose sorbent with chemically bound quinolin-8-ol

Preconcentration was effected using a 50 mm × 2 mm i.d. minicolumn packed with a spherical cellulose sorbent with chemically bound quinolin-8-ol function groups (Ostorb Oxin). The column was connected to the nebulizer of the atomic absorption spectrometer and the sample solution and eluent (2 M hydrochloric acid) were sucked through it at a flow-rate of 2–3 ml min^?1 by utilizing the negative pressure of the nebulizer. The experimental design was tested with the determination of traces of copper. Peak-area and peak-height measurements were compared. Owing to the simple calibration, the former method was used for quantification. The dynamic range was from 0.3 ng ml^?1 (detection limit) to 5 μg ml^?1 (breakthrough). The reproducibility in the concentration range 25 ng ml^?1-5 μg ml^?1 was better than 5%. Water-soluble inorganic salts, ammonia and sodium hydroxide were analysed. The accuracy of the results was checked by anodic-stripping voltammetry and by electrothermal AAS.     

Fluorimetric determination of oleandomycins with nicotinamide and 3-acetylpyridine

The method is based on a fluorescence reaction of the epoxy group with nicotinamide and 3-acetylpyridine. Oleandomycin phosphate and triacetyloleandomycin can be determined in the ranges 1–80 μg ml^?1and 5–80 μg ml^?1, respectively, with relative standard deviations of 3–5%. The method can be applied to pharmaceutical preparations. Results obtained by this method and by bioassay in an examination of residual potency agreed well when degradation was done under neutral or alkaline conditions.     

Fluorimetric determination of mebendazole and flubendazole in pharmaceutical dosage forms after alkaline hydrolysis

The selective and very sensitive fluorimetric determination of mebendazole and flubendazole is based on alkaline hydrolysis and adsorption on Whatman 42 filter paper. Limits of detection are 0.1 μg ml^?1 and 0.5 μg ml^?1, respectively, with linear response sponse up to 10 μg ml^?1 and 50 μg ml^t?1. The fluorescence produced is very stable (λ_em = 460 nm) and the method is applicable to anthelmintic pharmaceutical preparations.     

Spectrophotometric determination of copper with α, β, γ, δ-tetraphenylporphine trisulfonate

Water-soluble porphyrin, α, β, γ, δ-tetraphenylphorphine trisulfonate (TPPS, H₂R), was found to be a very useful agent for both the direct spectrophotometric determination and the photometric titration of copper(II). The molar absorptivity of H₄R²⁺ at 434 nm is 5.0·10⁵ and the spectrophotometric sensitivity is 0.00013 μg Cu cm^?2 for A=0.001. Beer's law is followed in the range 0.006 μg–0.06 μg Cu ml^?1. Among twenty-two elements examined, only zinc(II) seriously interfered. Acid dissociation constants and salt effects on the spectra of TPPS were evaluated.     

Extraction and spectrophotometric determination of niobium by tetraphenylarsonium and phosphonium chloride from a hydrochloric acid solution

The extraction of niobium(V) in the form of a chloro complex has been studied. Radiometrical and spectrophotometrical studies show that niobium(V) is extracted practically completely from a solution containing more than 9 mol dm^?3 chloride in the range of 2–5 M hydrogen ion concentration by chloroform solutions of tetraphenylarsonium (TPA) and tetraphenylphosphonium (TPP) chloride and that niobium is not extracted at chloride concentrations less than 6 mol dm^?3. The mechanism of extraction is based on the formation of the ion-associated compounds that form between the onium cation and the oxotetra-chloroniobate(V) anion. The extracted complexes in chloroform have a maximum absorbance at 282 nm (TPA) and 285 nm (TPP); they obey Beer's law in the range of 1–10 μg Nb ml^?1, and are stable for at least 24 hr. The molar absorptivity of the method is 1.33 × 10⁴ dm³ mol^?1cm^?1. The composition of the extracted species [(C₆H₅)₄X] [NbOCl₄] where X = As or P was determined spectrophotometrically, radiometrically, and by characterization of the crystalline compounds isolated.     

Application of a wave-guide capillary cell in the determination of copper by flow injection analysis

A wave-guide capillary cell is applied as a spectrophotometric detector in the flow-injection determination of copper(II). The copper solution is injected and sandwiched between zones of diethyldithiocarbamate (DDTC) solution in the carrier flow line. The Cu-DDTC complex formed is then extracted into carbon disulfide by means of an extraction coil followed by a teflon-membrane phase separator. Because carbon disulfide has a refractive index which is sufficiently higher than that of the fused silica from which the capillary cell is made, the light from the source propagates inside the capillary via total reflection at the inner cell wall as in an optical fiber. The detection limit for copper in the proposed system is 20 ng ml^?1 with linear response up to 1 μg ml^?1.     

Indirect atomic absorption spectrometric determination of perchlorate by liquid-liquid extraction in a flow-injection system

The determination is based on the continuous liquid-liquid extraction of the copper(I)/6-methylpicolinealdehyde azine/perchlorate ion-pair into 4-methyl-2-pentanone in a flow-injection manifold. The organic fills a loop of an injector situated in an integrated feed system of an atomic absorption spectrometer. Measurement of the copper atomic absorption signal from the organic phase allows the indirect determination of 0.5–5 μg ml^?1 perchlorate, giving a 3-fold increase in sensitivity over the conventional spectrophotometric method. The detection limit is 70 ng ml^?1. The sampling frequency is 45 ± 5 h^?1. The method is highly selective, and has been used for the determination of perchlorate added to serum and urine samples.     

Determination of technetium based on quenching of the fluorescence of some organic compounds,with application to vegetation

Technetium is an effective quencher of the fluorescence produced by 2,5-diphenyloxazole (PPO), 1,4-bis(4-methyl-5-phenyl-2-oxazolyl)benzene (POPOP) and 2,2′-pyridil [1,2-dioxo-1,2-bis(2-pyridyl)ethane]. Spectrofluorimetric procedures for 0.01–12 μg Tc ml^?1 with PPO and 0.1–12 μg ml^?1 with 2,2′-pyridil, and a spectrophotometric method for 1–15 μg ml^?1 are described. The distribution of technetium in vegetation is measured by applying the PPO method.     

Flow-injection chemiluminometric analysis of some steroids by their sensitizing effect on the bromate-sulphite reaction

The chemiluminescent oxidation of sulphite by bromate was investigated and compared with that by cerium(IV). The reaction is sensitized by various steroid hormones which can thus be determined in the ranges 0.50–20.0μg ml ¹ for cortisone; 0.50–5.00 μg ml^?1 for hydrocortisone and progesterone and 0.50–6.00 μg ml^?1 for testosterone and corticosterone.