Solvent extraction of Ru(III) with 2-mercaptobenzimidazole into n-butanol

A new and rapid method has been developed for the quantitative extraction of Ru(III) with 2-mercaptobenzimidazole into n-butanol. The extraction coefficient of Ru(III) between n-butanol and an ethanolic solution of 1% 2-mercaptobenzimidazole showed a maximum value ofE=161 at a pH of 2.0. The effect of various other parameters on the extraction coefficient value of Ru(III) such as solvent effect, anions, cations, etc. have also been studied. The stoichiometry of metal to reagent has also been determined by the method of substoichiometric extraction and by the slope ratio method and was found to be 1∶3. Decontamination factor for various elements in the substoichiometric extraction of Ru(III) were also evaluated.     

Solvent extraction of Au(III) using 2-mercaptobenzimidazole into n-butanol

A method has been developed for the extraction of Au(III) with 2-mercaptobenzimidazole into n-butanol.¹⁹⁹Au has been used as a tracer for establishing the ideal extraction parameters such as effect of pH, time of equilibration, solvents and anions. Separation factor and decontamination factor have also been evaluated to determine the selectivity of the method with respect to various elements. The interfering elements were suppressed by the use of suitable masking agents which increased the selectivity. The stoichiometry of metal to reagent was determined by the method of substoichiometric extraction and slope ratio method.     

A new and rapid method for the solvent extraction of Ru/III/ with 1,2,3-benzotriazole into 1-pentanol

A new and rapid method has been developed for the quantitative extraction of Ru/III/ with 1,2,3-benzotriazole /1,2,3-BT/ into 1-pentanol. The extraction coefficient value of Ru/III/ between 1-pentanol and an aqueous 5% solution of 1,2,3-BT in 2M sodium acetate-acetic acid buffer showed a maximum value of E=46 at pH 4.5. The effect of various other parameters on the extraction coefficient of Ru/III/ such as solvents, anions, cations, etc. have also been studied. The stoichiometry of metal:reagent determined by the method of substoichiometric extraction and slope ratio method was found to be 13. Decontamination factors for many elements in the substoichiometric extraction of Ru/III/ were also evaluated.     

Using NAA to the Determination of Antimony in Trichlorosilane with Substoichiometric Extraction

Neutron activation analysis has been applied to the determination of trace of antimony based on the substoichiometric extraction of Sb(III) with BPHA (N-benzoyl-N-phenyl hydroxylamine). The antimony contens in trichlorosilane or high purity silicon can be determined by the proposed method down to ppb range. The effect of acid concentration, shaking time, the amount of carrier and the decontamination factors were studied.     

Solvent extraction of Zn(II), Cu(II) and Sb(III) with N-m-tolyl-p-methoxybenzohydroxamic acid (TMBHA) into chloroform

Rapid methods have been described for the quantitative extraction of milligram amounts of Zn(II), Cu(II) and Sb(III) with TMBHA into chloroform. The separation factor for many elements was found to be at least greater than 10⁴. The metal: reagent stoichiometry determined by methods like slope ratio, mole ratio and substoichiometric extraction were found to be 12 for Zn(II) and Cu(II), and 23 for Sb(III).     

Substoichiometric Isotope Dilution Analysis for the Determination of Iron in Biological Materials and Comparison with Substoichiometric Isotope Dilution Mass Spectrometry

Substoichiometric isotope dilution analysis for the determination of trace iron has been studied by using synergistic extraction of iron(III) with a substoichiometric amount of 4-isopropyltropolone (Hipt) in the presence of an excess of 3,5-dichlorophenol (DCP) in heptane. Optimum conditions for the substoichiometric extraction of iron(III) in g to sub-g levels were examined and the high selectivity for iron(III) toward various metal ions encountered in the analysis of biological materials was confirmed. The present method was applied to a biological reference material (NIES, CRM No.9, sargasso) without any pre-separation and was successfully evaluated. Furthermore, substoichiometric stable isotope dilution mass spectrometry using the present extraction method was also used with the above sample. Applicability and practicability was compared for both substoichiometric methods.     

Substoichiometric and non-destructive determination of trace impurities in high-purity optical glasses by neutron activation analysis

A method of radioactivation analysis has been developed for the determination of 17 elements as impurities in high-purity optical glasses. The substoichiometric extraction of platinum with dithizone was studied and a simple procedure was proposed for the determination of platinum. Copper and manganese were also determined substoichiometrically by the extractions with dithizone and with thenoyltrifluoracetone, respectively. The non-destructive γ-ray spectrometry using a Ge(Li) detector has been applied for the determination of the other 14 elements (Ag, Co, Cr, Eu, Fe, Ir, Sc, Zn, Cs, Hf, Rb, Sb, Ta and Tb). Impurity elements at the ppb level were analysed by the proposed method and it is shown that the method is reliable for the determination of trace impurities in high-purity optical glasses.     

Solvent extraction of Os(IV) with 2-mercaptobenzothiazole into chloroform

2-mercaptobenzothiazole has been used for the solvent extraction of Os(IV) in acidic medium. The extraction of Os(IV) was found to be better than 90% over the pH range of 3.0 to 5.0 with an equilibration time of 5.0 minutes. The stoichiometry of metal:reagent determined by substoichiometric extraction and slope ratio method was found to be 1∶4. Decontamination factor for various elements in the substoichiometric extraction of Os(IV) were also evaluated.     

Radiochemical separation of Ru/III/ with 2-mercaptobenzothiazole into chloroform employing solvent extraction technique

The reagent 2-mercaptobenzothiazole /2-HMBT/ has been used for the solvent extraction of Ru/III/. The extraction coefficient value of Ru/III/ has been evaluated, based on various parameters such as, effect of molarity of the acid, time of equilibration, time of heating, effect of various solvents and effect of various salts. The stoichiometry of the metal to reagent was determined by the method of substoichiometric extraction of slope-ratio method and was found to be 13. Separation factor and decontamination factor for various elements have also been studied.     

Solvent extraction of cadmium/II/ with 2-mercaptobenzothiazole into methyl iso-butyl ketone

The extraction of cadmium/II/ with 2-mercaptobenzothiazole /2HMBT/ into methyl iso-butyl ketone has been studied. The effect of various parameters on the extraction coefficient value such as effect of pH, time of equilibration, effect of anions and cations have been evaluated. The stiochiometry of the extracted species obtained by the method of substoichiometric extraction and mole ratio method was found to be 1:2. Decontamination factors for a number of elements in the substoichiometric extraction of Cd/II/ were also obtained.     

A study on the solvent extraction of Se/IV/ with 2-mercaptobenzothiazole into chloroform

The extraction of Se/IV/ from hydrochloric acid medium with 2-mercaptobenzothiazole/2-HMBT/into chloroform has been studied. The effect of various parameters on the extraction coefficient value such as molarity of hydrochloric acid, time of equilibration, effect of cations and anions etc., has been evaluated. The stoichiometry of the extracted species was determined by the method of substoichiometric extraction and slope ratio method and was found to be 1∶4. Decontamination factors for many elements in the substoichiometric extraction of Se/IV/ was also obtained.     

Hollow fiber supported liquid membrane extraction coupled with thermospray flame furnace atomic absorption spectrometry for the speciation of Sb(III) and Sb(V) in environmental and biological samples

A new method of hollow fiber supported liquid membrane extraction (HF-SLME) coupled with thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) for the speciation of Sb(III) and Sb(V) in environmental and biological samples has been developed. The method is based on the complex of Sb(III) with sodium diethyldithiocarbamate (DDTC). The formed hydrophobic complex is subsequently extracted into the lumen of hollow fiber, whereas Sb(V) is remained in aqueous solutions. The extraction organic phase was injected into TS-FF-AAS for the determination of Sb(III). Total Sb concentration was determined after reduction of Sb(V) to Sb(III) in the presence of l-cysteine and the extraction procedure mentioned above. Sb(V) was calculated by subtracting of Sb(III) from the total Sb. DDTC was used as complexing reagent. 1-Octanol was immobilized in the pores of the polypropylene hollow fiber as liquid membrane and also used as the acceptor solution. Some parameters that influenced extraction and determination were evaluated in detail, such as concentration of sodium diethyldithiocarbamate (DDTC), type of organic solvent, pH of samples, stirring rates, extraction time, as well as interferences. Under optimized conditions, a detection limit of 0.8 ng mL⁻¹ and an enrichment factor of 160 were achieved. The relative standard deviation (RSD) was 6.2% for Sb(III) (50 ng mL⁻¹, n = 5). The proposed method was successfully applied to the speciation of Sb(III) and Sb(V) in environmental and biological samples with satisfactory results.     

Solvent extraction of Ni/II/ with isonitrosobenzoylacetone into chloroform

A method has been developed for the quantitative extraction of Ni/II/ with isonitrosobenzoylacetone /HINBA/ into chloroform. The effect of various parameters on the extraction coefficient value such as pH, time of equilibration, effect of solvents, anions, cations etc. have been studied. The stoichiometry of the metal: reagent determined by the method of substoichiometric extraction and slope ratio method was found to be 12. Decontamination factors for many elements in the substoichiometric extraction of Ni/II/ were also evaluated.     

A study on the solvent extraction of Cd/II/ with 1,2,3 benzotriazole into n-heptanol

The extraction of cadmium/II/ with 1,2,3 benzotriazole /2-BT/ into n-heptanol has been studied. The effect of various parameters such as effect of pH, time of equilibration, effect of anions on the extraction coefficient values have been evaluated. The stoichiometry of the extracted species by the method of substoichiometric extraction and slope ratio method was found to be 12. Decontamination factors for a number of elements in the substoichiometric extraction of Cd/II/ were also obtained.     

Determination of pentavalent antimony in antileishmaniotic drugs using an automated system for liquid-liquid extraction with on-line detection

An automated system for liquid–liquid extraction flow analysis (LLE-FA) for the determination of Sb(V) in antileishmanial drugs is presented. The method is based on extraction in a 5 mL glass extraction chamber of an ion pair formed between hexachloroantimoniate anion and rhodamine B cation into toluene. The detection system consists of a green light emitting diode (LED) and a photodiode. The system is controlled by a microcomputer using a program written in Visual Basic 3.0. The extraction process was optimized and the following experimental parameters were established: sample loop of 150 μL; reagent loop of 900 μL; stirring time of 100 s; phase separation time of 80 s; volumetric ratio of 1:1 (aqueous/organic). The method was in-house validated for the determination of Sb(V) in meglumine antimoniate. The following performance criteria were obtained: linearity of 0.9989, linear range of 7.0 × 10⁻⁵ to 7.2 × 10⁻⁴ mol Sb(V) L⁻¹, sensitivity of 1.61 × 10⁶ ± 2 arbitrary units L mol⁻¹ (P < 0.05), intra-assay precision of 3.5% (n = 5; 4.1 × 10⁻⁴ mol L⁻¹ Sb(V). Whereas the method is selective in the presence of Sb(III), As(III) and Pb(II) at concentrations up to one tenth of the concentration of Sb(V), As(V) interferes. The accuracy of the method was evaluated through comparison of results obtained from analyses of pharmaceutical formulations by the proposed LLE-FA method with those obtained by inductively coupled plasma optic emission spectrometry (ICP OES) and differential pulse polarography for total antimony and Sb(III), respectively. The proposed method presented an analytical frequency of eight analysis per hour and is suitable for Sb(V) determination in the quality control of drugs employed for the treatment of leishmaniasis.     

Solvent extraction of Tl/I/ with 2-mercaptobenzothiazole into chloroform

The extraction of Tl/I/ with 2-mercaptobenzothiazole into chloroform has been studied. The effect of various parameters on the extraction coefficient value has been evaluated. The stoichiometry of the extracted species obtained from the substoichiometric extraction was found to be 11. This war further supported by the slope ratio method. Decontamination factors of a number of elements in the substoichiometric extraction of Tl/I/ were also obtained.     

Development of a non-chromatographic method for the speciation analysis of inorganic antimony in mushroom samples by hydride generation atomic fluorescence spectrometry

A simple and sensitive method has been developed for the direct determination of toxic species of antimony in mushroom samples by hydride generation atomic fluorescence spectrometry (HG AFS). The determination of Sb(III) and Sb(V) was based on the efficiency of hydride generation employing NaBH₄, with and without a previous KI reduction, using proportional equations corresponding to the two different measurement conditions. The extraction efficiency of total antimony and the stability of Sb(III) and Sb(V) in different extraction media (nitric, sulfuric, hydrochloric, acetic acid, methanol and ethanol) were evaluated. Results demonstrated that, based on the extraction yield and the stability of extracts, 0.5 mol L^− 1 H₂SO₄ proved to be the best extracting solution for the speciation analysis of antimony in mushroom samples. The limits of detection of the developed methodology were 0.6 and 1.1 ng g^− 1 for Sb(III) and Sb(V), respectively. The relative standard derivation was 3.8% (14.7 ng g^− 1) for Sb(V) and 5.1% (4.6 ng g^− 1) for Sb(III). The recovery values obtained for Sb(III) and Sb(V) varied from 94 to 106% and from 98 to 105%, respectively. The method has been applied to determine Sb(III), Sb(V) and total Sb in five different mushroom samples; the Sb(III) content varied from 4.6 to 11.4 ng g^− 1 and Sb(V) from 14.7 to 21.2 ng g^− 1. The accuracy of the method was confirmed by the analysis of a certified reference material of tomato leaves.     

Substoichiometric isotope dilution analysis of arsenic in biological and environmental standard reference materials by solvent extraction using toluene-3,4-dithiol in benzene

A radiochemical solvent extraction procedure has been developed for the determination of As(III) using⁷⁶As tracer. It is based on the complexation of As(III) with toluene-3,4-dithiol (TDT) at pH 2 and subsequent extraction in benzene. The effect of various parameters such as pH, time of equilibration, nature of solvent, quantitative character and interferences have been studied. The method has been further developed into substoichiometric isotope dilution analysis for the determination of As at < 1 g level and employed for the analysis of several environmental and biological standard Reference Materials from NIST (USA), IAEA (Vienna) and NIES (Japan).     

Substoichiometric radioactivation analysis for ytterbium

The substoichiometric separation of Yb(III) can be achieved by the extraction of a substoichiometric amount of thenoyltrifluoroacetone and an excess amount of phenanthroline in benzene. The appropriate pH range for the substoichiometric extraction is 6–8. The reproducibility of the substoichiometric extraction of Yb(III) is very good as RSD 1%. As an example, Yb in a manganese nodule is determined by the substoichiometry combined with the radioactivation analysis. The content of Yb is 17.63±0.23 g/g. The present procedure can be applied to the determination of other rare earth elements.     

Substoichiometric separation and determination of trace metals

Substoichiometric methods are eminently suitable for the determination of many elements. As a new application of substoichiometry, a substoichiometric speciation of the element in different chemical states is proposed. Substoichiometric speciation of As(III) and As(V) is demonstrated as an example. This is based on a highly selective substoichiometric extraction of As(III) with thionalide and As(V) with tetraphenylarsonium chloride in the presence of an excess amount of pyrogallol. Coexistence of other diverse arsenic species including methylarsenic compounds does not give any interference to the selective determination of As(III) and As(V). For substoichiometric radioactivation, a novel application of the synergistic extraction system in a combination of a substoichiometric amount of thenoyltrifluoroacetone with an excess amount of phenanthroline is demonstrated for Yb as an example. Substoichiometric speciation based on the selective speration and an application of synergistic extraction to substoichiometric separation have additional possibilities in substoichiometry.