Liquid-liquid extraction of metal ions by the 6-membered N-containing macrocycle hexacyclen

The nitrogen-containing analogue of 18-crown-6, 1,4,7,10,13,16-hexa-azaoctadecane (hexacyclen)] was studied as a reagent for complexation and extraction of some metal ions. It was found that with this reagent and methyl isobutyl ketone, metal ions such as silver(I), mercury(II), copper(II), platinum(II) and palladium(II) can be quantitatively extracted and separated from iron(III) and some other metal ions.     

Solid-phase extraction of some heavy metal ions on a double-walled carbon nanotube disk and determination by flame atomic absorption spectrometry

A new preconcentration method was developed for the determination of trace amounts of Cu(II), Fe(III), Pb(II), Ni(II), and Cd(II) on a double-walled carbon nanotube disk. 4-(2-Thiazolylazo) resorcinol was used as a complexing reagent. The effects of parameters, including pH of the solutions, amounts of complexing reagent, eluent type, sample volume, flow rates of solutions, and matrix ions were examined for quantitative recoveries of the studied analyte ions. The retained metal ions were eluted by 2 M HNO3. The LOD values for the analytes were in the range of 0.7-4.4 microg/mL. Natural water samples and standard reference materials were analyzed by the presented method.     

Extraction of copper(II) with 1,2-diacylhydrazines in the presence of associated metals

Conditions of Cu(II), Zn(II), Ni(II), Co(II), and Fe(III) ions extraction (pH values, effect of reagent amount) with symmetrical 1,2-diacylhydrazines derived from straight-chain aliphatic carboxylic acids and α-branched higher carboxylic acids Versatic-10 were studied. The separation coefficients of element pairs and pH of half extraction were calculated. The values of [Cu(II)]: [reagent] ratios in extracted complexes were determined. 1,2-Diacylhydrazines were shown to be more selective extractants toward nonferrous metal ions as compared with carboxylic acids, while the branching and elongation of alkyl chain in the reagents enhances their extraction properties and compatibility with hydrocarbon solvents.     

Thiothenoyltrifluoroacetone: a new chelon

The thioderivative of 2-thenoyltrifluoroacetone, 1,1,1-trifluoro-4-(2-thienyl) 4-mercaptobut-3-en-2-one (STTA) was prepared. NMR and infrared spectra confirmed the previously suggested structure². The sulfur is attached to the carbon adjacent to the thienyl group and exists almost entirely in the thio-enolic form. The chelates of STTA with Ni(II), Cu(II), Pb(II), Zn(II). Co(II), Cd(II). Pd(II) and Hg(II) were prepared in a neutral to slightly basic medium, and characterized by analysis. NMR, infrared, visible and ultraviolet spectra, DTA, TGA and fractional sublimation. The chelates are relatively stable, insoluble in water, soluble in non-polar and some polar organic solvents, sublimable, and intensely colored compared to their normal diketone analogs. The selectivity of the reagent has not been completely established but divalent ions chelate more readily than trivalent ions; Fe(III), Al(III), Cr(III) apparently do not chelate. The new chelon may be useful as a color-developing reagent for the colorimetric analysis of such ions as Zn(II), Cd(II), Hg(II) and Pb(II). The molar extinction coefficients are given for the chelon and the chelates investigated     

Steady-state and flow-injection response of a metallic silver electrode for potentiometric detection of metal cyanide complex formartion

A metallic silver electrode provides a potentiometric response to Ag(I), Hg(II), Fe(III), Cu(II), Zn(II), Co(II) and Ni(II) ions, and large changes in the electrode potential of up to 400 mV are observed when these ions are injected into a 0.29 mM soulution of cyanide ion. Injection 10-μl aliquots into a reagent stream with a cyanide concentration of 0.1 mM is shown to give the expected sigmoidal-shaped response curve for peak height as a function of metal ion concentration. Sub-nanomole quantities of metal ions are detectable with a peak height of ca. 20 mV, depending on the cyanide concentration.     

Studies on the synthesis of 5-(p-aminobenzylidene)-rhodanine and its properties

A new analytical reagent 5-(p-aminobenzylidene)-rhodanine (ABR) was synthesized. The acidic dissociation constant of ABR has been determined. The properties, the acid-base behavior of ABR and the reactions of ABR with metallic ions have been studied. The color reactions of the reagent with Pd(II), Au(III), Ag(I), Ru(III), Hg(II) and Cu(II) are studied in detail. The composition of Pd(II)-ABR, Au(III)-ABR and Ag(I)-ABR complexes were discussed.     

Flotation-separation and ICP-AES determination of ultra trace amounts of copper, cadmium, nickel and cobalt using 2-aminocyclopentene-1-dithiocarboxylic acid.

A rapid flotation method for separation and enrichment of ultra trace amounts of copper(II), cadmium(II), nickel(II) and cobalt(II) ions from water samples is established. At pH 6.5 and with sodium dodecylsulfate used as a foaming reagent, Cu2+, Cd2+, Ni2+ and Co2+ were separated simultaneously with 2-aminocyclopentene-1-dithiocarboxylic acid (ACDA) added to 1 l of aqueous solution. The proposed procedure of preconcentration is applied prior to the determination of these four analytes using inductivity coupled plasma-atomic emission spectrometry (ICP-AES). The effects of pH, concentration of ACDA, applicability of different surfactants and foreign ions on the separation efficiency were investigated. The preconcentration factor of the method is 1000 and the detection limits of copper(II), cadmium(II), nickel(II) and cobalt(II) ions are 0.078, 0.075, 0.072 and 0.080 ng ml(-1), respectively.     

Liquid-liquid extraction of palladium(II) with N-n-octylaniline from hydrochloric acid media

N-n-Octylaniline in xylene is used for the extractive separation of palladium(II) from hydrochloric acid medium. Palladium(II) was extracted quantitatively with 10 ml of 2% reagent in xylene from 0.5-2 M hydrochloric acid medium. It was stripped from the organic phase with 1:1 ammonia and estimated spectrophotometrically with pyrimidine-2-thiol at 420 nm. The effects of metal ion, acids, reagent concentration and of various foreign ions have been investigated. The method affords binary separation of palladium(II) from iron(III), cobalt(II), nickel(II) and copper(II) and is applicable to the analysis of synthetic mixtures and alloys. The method is fast, accurate and precise.     

Studies on coordination polymers : Part I. Coordination polymers of 8,8'-dihydroxy-5,5'-biquinolyl

Coordination polymers of 8,8'-dihydroxy-5,5'-biquinolyl(I) with Cu(II), Zn(II), Cd(II), Ni(II), Co(II) and Mn(II) were prepared and studied. The polymers were all powders, very insoluble in all the common organic solvents, apparently of low molecular weight and all began to decompose between 250–300°. The polymers of cobalt and nickel were amorphous, whereas the polymers of copper, zinc, cadmium and manganese were crystalline. Infrared studies confirmed the chelation reaction between metal and (I). As a spot test reagent, (I)gave instant color reactions with 14 common ions but the sensitivity of the reagent is not particularly impressive. The most interesting result is the detection of 2 μg of gallium.     

Extraction and separation studies of platinum(IV) with N-n-octylaniline

N-n-octylaniline in xylene is used for the extractive separation of platinum(IV) from acidic media. Platinum(IV) was extracted quantitatively with 10 ml of 3% reagent in xylene from 0.5 to 10 and 2.5 to 10 M hydrochloric and sulphuric acid, respectively. It was stripped from organic phase with water and estimated photometrically with stannous chloride. The effect of metal ion, acids, reagent concentration and of various foreign ions has been investigated. The method affords binary separation of platinum(IV) from iron(III), cobalt(II), nickel(II) and copper(II), and is applicable to the analysis of synthetic mixtures and alloys. The method is fast, accurate and precise.     

8-Quinolinol-5-sulfonic acid-loaded resin as a preconcentrating agent in the neutron activation analysis of the chalcophile elements (author's transl)]

A chelating agent-loaded resin consisting of 8-quinolinol-5-sulfonic acid and an anion-exchange resin (HOx-resin) was prepared in order to concentrate trace chalcophile elements in natural water samples selectively before neutron activation analysis. The exchange capacity of the Diaion SA No. 100 for the reagent (1.8 meq . g-1 resin) corresponds approximately to that for chloride ion (1.83 meq . g-1 resin), indicating that 8-quinolinol-5-sulfonic acid is adsorbed quantitatively on the exchange site of the resin through the sulfonate anion in the reagent. The basic conditions for the adsorption of the metal ions on the resin were investigated by employing the column method. The nitrate concentration and the pH of the sample solution affect the adsorption behavior of metal ions. Several solutions containing metal ions with varying pH or varying nitrate concentration were applied to the resin column (35 mm x 7 mm phi) with a flow rate of 2.0 cm3 . min-1. As a result, the optimum conditions for the quantitative adsorption of copper(II), zinc(II), cadmium(II), cobalt(II), nickel(II) and manganese(II) were as follows: NO3- less than 0.01 mol . dm-3 pH greater than 4.6. Furthermore, the feasibility of the above conditions as well as quantitative adsorption of the chalcophile elements was confirmed through the neutron activation analysis of the synthesized metal solutions.     

Use of tetracyanoplatinate (ii) for the luminescent detection of metalions

The tetracyanoplatinate(II) (TCP) ion forms insoluble fluorescent compounds with many metal ions. This property has not hitherto been exploited for analytical use. The soluble sodium TCP salt has been applied as a reagent for metal ion detection. Fluorescent precipitates useful for detection of the metal ions were obtained with Y(III), Zr(IV), Ag(I), Zn(II), Cd(II), Hg(I), Hg(II), A1(III), Pb(II), La(III) and Th(IV). Limits of detection ranged from 5 to 200 ppm. With ammonium acetate as a masking agent, selective detection of 10 ppm of silver was achieved in the presence of the other metal ions. As little as 20 ppm of zirconium can be detected in the presence of hafnium, which yields a non-fluorescent precipitate.     

Palladium(II) Extraction from Hydrochloric Acid Solutions with 4-[(Hexylsulfanyl)methyl]-3,5-Dimethyl-1H-Pyrazole

Palladium(II) extraction from hydrochloric acid solutions with a novel weakly basic complexing reagent, 4-[(hexylsulfanyl)methyl]-3,5-dimethyl-1H-pyrazole, dissolved in chloroform was studied. Palladium(II) was found to be highly efficiently extracted from 0.1–3 mol/L HCl solutions. A coordination mechanism of palladium(II) extraction with a protonated form of the reagent via fast interphase transfer of ion associates was proposed. The composition of the extracted compound, [PdCl₂μ-L]_n (n > 2), was found, and the way of coordination of the reagent to metal ions through N(2) nitrogen atom and thioether sulfur atom was determined. The reagent can be recommended for concentrating palladium(II) and selectively separating it from platinum(IV), copper(II), nickel(II), and iron(III).     

Analytical possibilities of pyridine-2-acetaldehyde benzoylhydrazone as a chromogenic reagent

With a view to the use of pyridine-2-acetaldehyde benzoylhydrazone is an analytical reagent, a study of the physical properties and fundamental solution chemistry of the complexes formed by PABH with Fe(II), Fe(III), Ni(II), Pd(II), V(V), Ti(IV), Hg(II), Mn(II), Zn(II), Bi(III), Co(II), Cu(II), Pb(II), and Ga(III) metal ions has been carried out. A critical comparison of pyridine-2-carbaldehyde and pyridine-2-acetaldehyde salicyloylhydrazones and pyridine-2-acetaldehyde benzoylhydrazone as analytical reagents is given.     

Negative ion chemical ionization mass spectrometric studies of tetradentate schiff base coordination compounds. Fluorinecontaining reagent gases

Negative ion mass spectra using chemical ionization conditions have been measured for a series of tetradentate Schiff base corrdination compounds of Co(II), Ni(II) and Cu(II). Fluorine-containing reagent gases CF₄, SO₂F₂ and SF₆ have been used. The formation of molecular negative ions for the complexes is dependent on the reagent gas used. The secondary ions detected are produced by incorporation of CF₃, F and F₂ species into the coordination compounds.     

Liquid-liquid extraction study of tellurium(IV) with N-n-octylaniline in halide medium and its separation from real samples

N-n-Octylaniline in xylene is used for extractive separation of tellurium(IV) from hydrochloric acid media. Tellurium(IV) is extracted quantitatively with the 3% reagent in xylene from 5.5 to 7.5 M hydrochloric acid. It is stripped from organic phase with 1:1 ammonia and estimated spectrophotometrically with pyrimidine-2-thiol (4'-bromoPTPT). The effects of metal ion, acids, reagent concentration, diluents and various foreign ions have been investigated. The log-log plots of distribution ratio (D(Te(IV))) versus N-n-octylaniline concentration indicate that the nature of extracted species is [(RR'NH(2)(+))(2) TeCl(6)(2-)](org). The method affords binary separation of tellurium(IV) from gold(III), selenium(IV), bismuth(III), copper(II), lead(II), antimony(III), germanium(IV) and is applicable to the analyses of synthetic mixture containing associated metal ions and alloy samples. The method is simple, selective, rapid and accurate.     

Studies on coordination polymers : Part II. Coordination polymers of 1,6-dihydroxyphenazine

Coordination polymers of 1, 6-dihydroxyphenazine (I) with Cu(II), Zn(II), Ni (II), Co(II) and Hg(II) were prepared and studied. All the polymers formed were dark blue to black powders, very insoluble in the common solvents, apparently of low molecular weight, and decomposed at temperatures ranging from 200 to 280°. The zinc polymer was the most stable, mercury the least. Infrared studies confirmed the proposed chelation reaction between the metal ion and (I). The polymers of Co and Hg were amorphous, whereas those of Cu, Zn, and Ni were crystalline. When used as a spot test reagent, (I) gave instant color reactions with 15 common ions but neither the sensitivity nor selectivity of the reagent is impressive.     

Metal complexes of 4-(2'-thiazolylazo)-resorcinol A comparative study with 4-(2'-pyridylazo)-resorcinol

The acid dissociation constants of 4-(2'-thiazolylazo)-resorcinol (TAR) and the formation constants of the metal complexes formed by this reagent with Cu(II), Ni(II), Co(II), Zn(II) and Mn(II) have been determined potentiometrically at 25° in 50% v/v mixtures of dioxane and water. The values obtained for TAR and the metal complexes are contrasted with similar values for the reagent 4-(2'-pyridylazo)-resorcinol (PAR). Differences and similarities between the co-ordinating tendencies of these two reagents are revealed in terms of the proton displacement constant and the acid dissociation constants of the metal complexes. Evidence is presented which suggests that both TAR and PAR may act as terdentate ligands toward some bivalent metal ions.     

2-Thion-5-mercapto-1,3,4-thiadiazolidin als Reagens für die photometrische Bestimmung von Platin(IV), Palladium(II) und Osmium(VIII)

A method for the photometric determination of platinum(IV), palladium(II) and osmium(VIII) with 5-mercapto-thiadiazolidine-thione-2 is described. The effects of an excess of reagent, of time, pH and of diverse ions were studied. The optimum concentration range for the method is 10 to 100 Μg of Pt(IV), Pd(II) and Os(VIII).     

Cation complexation with p-tert-butylcalix[5]arene pentacarboxylic acid derivative: an allosteric regulation of the first metal ion for stepwise extraction of the second ion

A calix[5]arene based solvent extraction reagent 3, appending carboxylic acid groups at the lower rim, has been developed and its complexation behavior towards some transition metal ions has been studied. The host 3 can selectively and quantitatively extract Pb(II) ions above pH 1.8 while other divalent ions such as Cu(II), Zn(II), Co(II), Ni(II) are extracted quantitatively only above pH 3.0. The outstanding Pb(II) selectivity of 3 comes from the size fit complementarity effect of the Pb(II) ion in the calix[5]arene cavity. One molecule of 3 extracts two Pb(II) ions in a stepwise manner. The first Pb(II) ion is extracted into the deep cavity of the calix[5]arene defined by phenoxy oxygen atoms. The first complexed Pb(II) ion acts as a template to bring the host into a cone conformation and induces a positive allosteric effect for the extraction of the second Pb(II) ion at an oxygen rich coordinating site composed of carboxyl groups. Both the Pb(II) ions are extracted through an ion exchange mechanism and the electroneutral complex in the organic phase is formed by the release of an equivalent number of hydrogen ions into aqueous solution. The loaded Pb(II) is easily back-extracted from Pb(II)-complexed 3 using dilute acid solution.