Journal of Radioanalytical and Nuclear Chemistry, Articles ...
Journal of Radioanalytical and Nuclear Chemistry, Articles, Vol. 152, No. 1 (1991) 117-126
SEPERATION OF METALLIC IMPURITIES FROM URANIUM BY ANION EXCHANGE ON DOWEX 1 X 8 RESIN
R.J. ROSENBERG, A.-M. FORSBACKA, N.GRAS
(Received August 7, 1990)
The separation of metallic impurities from uranium by anion exchange with a Dowex 1 X 8 resin has been investigated. The following elements can be quantitatively separated from 400 mg uranium using a 1 cm diameter 15 or 30 cm long column. The elements Ag, Al, Ba, Ca, Cr, Cs, K, Mg, Mn, Na, Ni, Rb, REE, Sc, Th, Ti, and Y can be seperated by eluting the elements with conc. HCl. Uranium is retained by the resin. Al, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Na, REE and V can be seperated by eluting with 0.01 N H2SO4. Uranium is retained by the resin. Cd and Zn can be seperatedby first eluting uranium with 0.5 N HCl and then eluting Cd and Zn with 1 N NH3. Hf, Zr, and V can be separated by eluting with 5 N HCl but some uranium contamination is unavoidable.
Journal of Chromatography A. 874 (2000) 311-317
Short communication
SEPARATION AND DETERMINATION OF RARE EARTH ELEMENTS BY DOWEX 2-X8 RESIN USING SODIUM TRIMETAPHOSPHATE AS ELUTION AGENT
Sana Kutun Sungur, Aycicek Akseli
(Updated Jauary 26, 2000)
The distribution coefficients of rare earth elements amd thorium with Dowex 2-X8, 200-400 mesh, a strongly basic anion-exchange resin, have been determined regarding four different concentrations of sodium trimetaphosphate (3x10-3, 5x10-3, 7x10-3 and 0.01 M). The separation of the rare earths and thorium obtained from an Australian monazite has been investigated by anion-exchange chromatography with sodium trimetaphosphate concentration gradient on a Dowex 2-X8 Dowex 1 resin. The elution was investigated using 5 mg and 250 mg samples. In the separation of 5 mg samples, all elements were seperated in 29 min. It has been seen that the elution peaks are narrow, tailing effects are very small. Dy and Y are well separated. Qualitative and quantitative determinations were realized by spectrofluorometry. 2000 Published by Elsevier Science B.V. All rights reserved.
JOURNAL OF CHROMATOGRAPHY
ANION EXCHANGE CHROMATOGRAPHY OF TRANSITION METALS IN TARTRATE MEDIUM
GERALD P. MORIE AND THOMAS R. SWEET,
(Received January 27TH, 1964)
The tartrate complexes of chromium , molybdenum, nickel, silver, cadmium and mercury were studied by the batch equilibration method on Dowex 2x-8 anion exchange resin. From the distribution coefficients obtained for the above metals and for manganese, cobalt, zinc and iron, several column separations were developed. Radioisotopes were used in the batch equilibration studies and in the chromatographic separations.
ANALYST, FEBUARY 1989, VOL.114
DETERMINATION OF IRON SPECIES IN WINE BY ION-EXCHANGE CHROMATOGRAPHY – FLAME ATOMIC ABSORPTION SPECTROMETRY
Radmila Ajlec and Janez Stupar
The direct coupling of ion-exchange chromatography to flame atomic absorption spectrometry (AAS) has been achieved by employing a Babington type nebuliser. The system enables all the processes on the column to be followed directly at flow-rates of between 1 and 5ml min-1. The potential of the system was investigated for the determination of various iron species in synthetic samples containing iron(II) and iron(III) in ionic or chelated form by employing various ion-exchange (Dowex 50-X8, Dowex 1-X8) and sorptive (Amberlite XAD-2) resins, respectively. In some instances where direct coupling was impossible, owing to the physical properties of effluent or eluent, conventional analyses of chromatography separated iron species were preformed by flame AAS. The optimum concentration range, limit of detection and reproducibility of measurement were also determined for a particular column capacity. When direct coupling was employed, the detection limit for the separated iron species was 15 (g with a relative standard deviation (RSD) of -+3% and, using the conventional method of analysis, 2-5 (g with an RSD of -+1%. On the basis of these results the system was applied to the determination of the ratio of iron(II) to iron(III) in wines.
Analytica Chimica Acta, 138 (1982) 285-294
ACCURATE DETERMINATION OF TRACE AMOUNTS OF THORIUM IN SILICATE ROCKS BY CATION-EXCHANGE CHROMATOGRAPHY AND SPECTROPHOTOMETRY
A.H. VICTOR and F.W.E. STRELOW
October 30, 1981
Thorium in four of the South African NIMROC standards and in four secondary standards is determined accurately by means of spectrophotometry with arsenazo-III after a selective cation-exchange seperation on an AG50W-X4 resin column. All other elements are eluted with 6 M hydrobromic acid before the final elution of thorium woth 5M nitric acid. Small amounts of zirconium which may be presant in the thorium eluate, are effectively complexed with oxalic acid which eliminates the spectrophotometric interferences caused by organic material leached from the resin column. The accuracy and precision of the method are demonstrated by the analysis of synthetic mixtures containing various amounts of thorium. Amounts of 10 and 100 (g of thorium can finally be determined with coefficients of variation of 1% and 0.2%, respectively.
Analytica Chimica Acta, 215 (1988) 317-323
DETERMINATION OF TRACE ELEMENTS IN MANGANESE METAL AND COMPOUNDS BY ION-EXCHANGE CHROMATOGRAPHY AND ATOMIC ABSORPTION SPECTROMETRY
A.M.M.M. FAISCA and A.H. VICTOR
July 28th, 1987
Traces of the specified elements are separated from 1g of manganese(II), using a 30-g column of AG50W-X8 cation-exchange resin and mixtures of hydrochloric acid and acetone as eluents. The trace elements are separated into three groups and are determined by atomic absorption spectrometry, except uranium for which spectrophotometry is used. Recoveries for 10 (g amounts (20 (g for gallium) vary between 94% (for gallium) and 103% (for uranium). A combined elution curve, results for the analysis of synthetic mixtures and for the determination of ten trace elements in samples of manganese metal, chloride and dioxide are presented.
Analytica Chimica Acta 290 (1994) 371-377
PRECONCENTRATION OF TRACE ELEMENTS FROM HIGH-PURITY THORIUM AND URANIUM ON CHELEX-100 AND DETERMINATION BY GRAPHITE FURNACE ATOMIC ABSORPTION SPECTROMETRY WITH ZEEMAN-EFFECT BACKGROUND CORRECTION
Naina Raje, Satish Kayasth, T.P.S. Asari, S. Gangadharan
November 30th, 1993
Preconcentration of trace impurities from large-sized samples of uranium metal and thorium oxide using a small column of Chelex-100 followed by their determination using graphite furnace atomic absorption spectrometry (GFAAS) is reported. A 0.5-10-g amount of the sample (uranium metal of thorium oxide) was dissolved, complexed with ammonium carbonate and subjected to the ion-exchange procedure. The retained analytes were eluted with 2-4 M nitric acid and brought to a small volume for a final dilution to 10-25 ml for their determination using GFASS. The validity of the separation procedure and recoveries at (g kg-1 levels was checked by standard addition; the recoveries were > 95%.
Analyst, January 1990, VOL.115
DETERMINATION OF TRACE AMOUNTS OF CADMIUM, LEAD, COPPER AND ZINC IN NATURAL WATERS BY INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION SPECTROMETRY WITH THERMOSPRAY NEBULISATON, AFTER ENRICHMENT ON CHELEX-100
Koen Vermeiren, Carlo Vandecasteele and Richard Dams
Enrichment on Chelex-100, followed by evaporation when necessary, was used for the pre-concentration of Cd, Pb, Cu, and Zn from natural waters. The measurements were carried out with inductively coupled plasma atomic emission spectrometry using a thermospray nebulisation system to reach the required sensitivity. The detection limits corresponding to three times the standard deviation of the blank (in 1% v/v HNO3) after a 30-fold enrichment are 0.02 (g 1-1 for Cd, 0.33 (g 1-1 for Cu and Zn. Matrix effects, which are fairly serious with thermospray nebulisation, were taken into account by using the standard additions method. Results obtained for several river water samples were compared with those found by analysis of thenon-enriched sample with inductively coupled plasma mass spectrometry or graphite furnace atomic absorption spectrometry. In all instances the agreement was satisfactory.
Journal of Radioanalytical and Nuclear Chemistry, Articles, Vol. 172, no. 1 (1993) 43-48
SORPTION OF SILVER IONS BY CHELEX 100 CHELATING RESIN
R.N.Ceo, M.R. Kazerouni, K. Rengan
June 3, 1992
Cationic species
At pH 3, however, carboxyl groups begin to deprotonate and complete sorption occurs. The silver is gradually eluted at pH 7 and above. The elution may be due to competion between the resin’s functional groups and ammonia molecules in solution. The effect is more pronounced at pH 9, since the increase in [OH-] causes an equillibrium shift favoring formation of molecular ammonia. The results are consistent with the change of distribution coefficients with pH reported by YOSHIZUKA et al.7 Their results predict strong sorption from ammoniacal solutions around pH 5 and weak sorption at pH8, as observed in our experiments.
Anionic species
At low chloride concentration, Chelex 100 sorbs silver efficiently. Silver exists in these solutions as an anionic complex, sorption is efficient even up to pH 7. Presumably the exchange occurs at the NH+ site. The results reported here are consistent with the values reported by KHUN and HERING3 and by RILEY and TAYLOR.4 GOYA and LAI6 reported 43.3% sorption of silver. However they used a batch process with 0.25g of resin for 20 ml of seawater. The small amount of resin used (approximately 3% of those used in other investigations) may account for the low sorption. The low sorption reported by DAVEY et al.5 is not consistent with other results of the presant work, perhaps due to the high flow rate.
At higher [CL-], sorption is poor. This may be because the resin beads shrink, rendering the interior functional groups inaccessible and reducing ion exchange capacity. Since the amount of dissolved silver is small compared to the resin’s capacity, this effect is not significant. It is likely that chloride ions occupy all the available anion exchange sites and the excess chloride ions occupy all the available anion exchange sites and the excess chloride shifts the solution/resin equilibrium so that the silver ions stay in solution.
Thiocyanate ions form strong bonds to silver ions, and their sorption to Chelex 100 is quite different from that of the chloro complexes. Sorption of silver from thiocyanate solutions decreases with increasing pH and with increasing ligand concentration. The concentration dependence has been determined in the pH range where the resin functions as both cation and anion exchanger. Two factors may be responsible: anion sorption decreases at higher pH, and any cations which sorb to the resin are rapidly eluted by complexation with the thiocyanate ions.
Journal of Radioanalytical and Nuclear Chemistry, Articles, Vol. 209, No.1 (1996)
157-159
ION EXCHANGE STUDIES OF U(VI) FROM AQUEOUS ARSENAZO-III SOLUTIONS USING AG-2X8, DOWEX-50WX8 AND CHELEX-100 RESINS
F.H.EL-SWEIFY, N.A.TADROS
(April 16, 1996)
The distribution of U(VI) between the anion exchanger Dowex-50WX8 and the chelating resin Chelex-100 and aqueous solutions of Arsenazo-III at different pH values was studied. The concentration of the Arsenazo-III was in the range of 1.53 x 10-4-1.23 x 10-3M. Equilibrium pH was varied from 1.0 to 8.78 while U(VI) original concentration was held at a constant at 3.39 x 10-4M. The effect of Arsenazo-III concentration and the variation of hydrogen ion concentration on U(VI) species formed in a solution as well as the sorbed species was discussed. Use was made of IR spectroscopy to investigate the sorption behavior. The sorption of some interfering ions such as Th(IV), Zr(IV), and Ce(III) on the resins used at optimum conditions for the sorption of U(VI) was also investigated.
Analytica Chimica Acta 375 (1998) 293-298
DETERMINATION OF METALS IN HIGHLY SALINE MATRICES BY SOLID-PHASE EXTRACTION AND SLURRY-SAMPLING INDUCTIVELY COUPLED PLASMA-ATOMIC EMISSION SPECTROMETRY
O. ABOLLINO, M. ACETO, M.C. BRUZZONITI, E. MENTASTI, C. SARAZANINI
April 28, 1998
Matrix removal and preconcentration of metals from liguid samples were obtained with a solid-phase extraction/slurry-sampling procedure applied to inductively coupled plasma-atomic emission spectrometry (ICS-AES) detection. A polymeric, adsorbing resin (Amberlite XAD-2), dispersed in the sample, was used for total sorption of analytes previously complexed with a dithiocarbamate ligand. After filtration, the resin was recovered and re-dispersed by means of a non-ionic surfactant: metals retained were determined with the slurry-sampling technique. All parameters were optimised to yield a solution-like signal from the final dispersion. © 1998 Elsevier Science B.V. All rights reserved.
Talanta, 1961, Vol.8, pp. 143 to 162. Pergamon Press Ltd.
Analytica Chimica Acta 375 (1998) 299-306
SPECIATION OF COPPER AND MANGANESE IN MILK BY SOLID-PHASE EXTRACTION/ INDUCTIVELY COUPLED PLASMA-ATOMIC EMISSION SPECTROMETRY
O. ABOLLINO, M. ACETO, M.C. BRUZZONITI, E. MENTASTI, C. SARZANINI
April 28, 1998
A speciation method was developed to study distribution of copper and manganese species in cow milk. The method is based upon solid-phase extraction of selective fractions of the analytes, followed by elution and determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES), using it as a flow-injection detector. Fractions detected were cationic, anionic, neutral and casein-bound. A different behavior is observed for the two metals. © 1998 Elsevier Science B.V. All rights reserved.
Analytica Chimica Acta, 83 (1976) 111-118
ATOMIC-ABSORPTION DETERMINATION OF VANADIUM AND MOLYBDENUM IN TAP WATER AND MINERAL WATERS AFTER ANION-EXCHANGE SEPERATION
J. KORKISCH & H. KRIVANEC
November 10, 1975
A method is described for the determination of vanadium and molybdenum in samples of tap and bottled mineral water. After acidification with citric acid the water sample is heated to about 80*C to remove CO2; sodium citrate and ascorbic acid are added and the resulting solution of pH 3 is passed through a column of the strongly basic anion-exchange resin Dowex 1-X8 (cirate form) on which both vanadium and molybdnum are adsorbed as anionic citrate complexes. Vanadium is eluted with 6M hydrochloric acid; molybdenum is recovered with 2M perchloric acid—1 M hydrochloric acid. Vanadium and molybdenum are determined in the eluates by atomic-absorption spectrometry. The samples analysed contained 0.1—0.9 (g 1-1 molybdenum.
Talanta, 1961, Vol.8, pp. 143 to 162
NON-AQUEOUS SOLVENTS IN ANION-EXCHANGE SEPERATIONS
JAMES S. FRITZ AND DONALD J. PIETRZYK
October 13, 1960
Distribution coeffcients are measured for the partition of metal ions between anion-exchange resin and organic solvent-water mixtures containing hydrochloric acid. The presence of an organic solvent causes metal ions to be taken up at lower hydrochloric acid concentrations. In many cases, distribution coefficients are significantly higher than in water-hydrochloric acid systems. If other conditions are comparable, the order of distribution coefficients in alcohol-water-hydrochloric acid is: isopropyl > ethyl > methyl alcohol. Column seperations of metal ion mixtures can be carried out by eluting with alcohol-water-hydrochloric acid mixtures of different compositions. Successful seperations of a number of mixtures are reported.
Analyst, January 1997, Vol. 122 (19-26)
ASSESSMENT OF DOWEX 1-X8-BASED ANION-EXCHANGE PROCEDURES FOR THE SEPERATION AND DETERMINATION OF RUTHENIUM, RHODIUM, PALLADIUM, AND GOLD IN GEOLOGICAL SAMPLES BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY
IAN JARVIS, MARINA M. TOTLAND AND KYM E. JARVIS
Synthetic multielement solutions of the plainum group metals (PGE: Ru; Rh; Pd; Ir; Pt;) and gold, with analysis by ICP-AES and ICP-MS, have been used to study the behavior of the precious metals on Dowex 1-X8 resin. Simple solutions of precious-metal chlorocomplexes showed near-complete adsorption (>99%) of most ((5%). Solutions pre-treated with acid mixtures typically used to decompose geological samples, demonstrated that perchloric acid adversely affects the adsorption of the PGEs on the resin. Solutions treated with HF-HNO3-HCl maintained good retention of Ir, Pt, Au (>99%), Pd (>94%) and Ru (>90%), but displayed significant loss (up to 40%) of Rh. A two-step procedure was necessary to elute the precious metals from the resin: 0.3 mol 1- thiourea prepared in 0.1 mol-1 HCl removed Ru, Pd, Pt, Au, and some Rh: 12 mol 1-1 HCl eluted remaining Rh and all Ir. Recoveries ranged from 50 to 100%. At low levels, the determination of PGE and Au in the thiourea fraction by ICP-MS was compromised by high levels of total dissolved solids (TDS), which necessitated dilution of the eluate prior to analysis. The TDS was reduced by decomposing thiourea with HNO3 and removing SO42- by precipitation of BaSO4, but this led to lower and more erratic results, and increased contamination. An assessment of the optimised procedure employing geological reference materials PTM-1, PTC-1 and SARM7, indicated that acceptable results should be attainable for ICP-MS determination of most elements in geological samples containing high concentrations (>1 (g g –1) of the PGE, for which decomposition of thiourea is unnecessary. The addition of a decomposition step led to low recovery of all elements except Ir, which was presant entirely in the HCl eluate. The method is viable for the determination of Ir in a range of geological materials, but modifications will be required if it is to be extended to the other precious metals.
Marine Chemistry, 29 (1990) 295-306
A LOW CONTAMINATION CHELEX-100 TECHNIQUE FOR SHIPBOARD PRE-CONCENTRATION OF HEAVY METALS IN SEAWATER
SU-CHENG PAI, TIEN-HIS FANG; CHENG-TUNG A. CHEN & KWUNG-LUNG JENG
January 16, 1990
An easy to handle, on-board procedure is proposed which uses a Chelex-100 ion-exchange column to pre-concentrate Cd, Co, Cu, Fe, Mn, Ni, Pb, and Zn from seawater with minimal risk of contamination. Immediately after collection, the seawater sample is poured into a polyethylene terephthalate (PET) bottle containing ammonium maleate buffer at pH 6.5. The bottle is then connected to a pre-packed Chelex-100 column set, and hung upside-down to allow the sample to flow through the column in dust-free conditions. Finally, the whole batch of columns is brought back to the land-based laboratory for further elution and analysis. A concentration factor of 250 is achieved.
Journal or Analytical Atomic Spectrometry, April 1993, Vol.8
DETERMINATION OF LEAD ISOTOPE RATIOS AND CONCENTRATIONS IN SEA-WATER BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY AFTER PRECONCENTRATION USING CHELEX-100
AKIRA MIYAZAKI AND RAUL A. REMIER
The determination of lead isotope ratiosand concentrations in open and coastal sea-water by a combination of chelating resin (Chelex-100) preconcentration and inductively coupled plasma mass spectrometry is described. The 206Pb: 204Pb, 208Pb:204, 207Pb:208Pb and 206Pb:207Pb isotope ratios were measured with relative standard deviations of 1.2, 0.9, 0.1 and 0.3%, respectively. The accuracy of the isotope data was checked with reference materials, National Research Council Canada NASS-3 Open Ocean Sea-water and National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) 981 Lead, Common Isotope, and compared with those in other work. The results revealed that the proposed method was applicable to the measurement of lead isotope ratios in sea-water with precision adequate to be able to discuss the origin of lead.
Analytical Chemistry, Vol. 50, NO. 9, August 1978
DISTRIBUTION COEFFICIENTS AND ANION EXCHANGE BEHAVIOR OF SOME ELEMENTS IN HYDROBROMIC-NITRIC ACID MIXTURES
F.W.E. STRELOW
Anion exchange distribution coefficients with Bio-Rad AG1-X8, a quaternary amine resin on polystyrene basis, are presented for the elements Bi(III), Cd, Pb(II), Zn, and In(III) In hydrobromic-nitric acid mixtures ranging from 0.03 to 1M hydrobromic and nil to 2M nitric acid. The results are discussed and some possible separations are pointed out. The versatility of these eluting mixtures is demonstrated by sequential elution of Zn, Pb(II), Cd, and Bl(III) from a 11.5-mL resin column using appropriate eluting agent concentrations.
Analytica Chimica Acta, Vol. 20 (1959) 271-274
THE DETERMINATION OF NICKEL, COBALT, IRON AND ZINC IN FERRITES
DONALD H. WILKINS
An anion exchange technique has been developed for the determination of iron, nickel, cobalt and zinc in a ferrite type material. The constituents are seperated by utilizing the differences in the adsorption of their chloride complexes on a strongly basic anion exchange resin. Each constitent is determined by the back titration of an excess of EDTA with a standard copper solution, using PAN as an indicator.
Analytical Chemistry, Vol. 39, NO.6, May 1967 (595-599)
ANION EXCHANGE AND A SELECTIIVITY SCALE FOR ELEMENTS IN SULFURIC ACID MEDIA WITH A STRONGLY BASIC RESIN
F.W.E. STRELOW AND C.J.C. BOTHMA
Anion exchange equilibrium distribution coefficients with Bio-Rad AG1-X8, 100- to 200-mesh, a quaternary ammonium resin in the sulfate form, are presented for 52 elements in sulfuric acid media. The acid concentration range from 0.01N to 4.0N is covered. Coefficients for elements with strong hydrolytic tendencies like Ta(V), Nb(V), and W(Vl) are determined in the presence of H2O2. The elements are arranged arbitrarily into a selectivity scale according to distribution coefficients in 1.0N acid, or according to the coefficients are ................
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