Essential serum trace metals: II. Determination of copper and zinc

Several complexing ligands for copper and zinc were tested for their feasibility as analytical reagents. Of these, tetraethylthiuram disulfide and its analog, bis (1-piperi-dylthiocarbonyl) disulfide were selected for copper with some advantages determined to accrue to each. Two others, 1-(2-pyridylazo)-2-naphthol and 1-[(5-chloro-2-pyridyl) azo]-2-naphthol were selected for zinc with the preference given to the former for stability of color formed and accessibility of the reagent although the chloro analog is inherently the more sensitive of the two reagents. For those who do not have atomic absorption spectrophotometry at their disposal, the molecular absorption approach still appears to be an excellent one with good selectivity for the two metals described.     

Determination of trace metals by capillary electrophoresis

A new analytical procedure is developed using a strong complexing agent, 1,10-phenanthroline (Phen), for direct UV detection of Zn, Mn, Cu, Co, Cd, and Fe at microg/L concentrations in environmental water samples. The metal chelates formed showed different electrophoretic mobilities and solved the comigration problem for capillary electrophoresis (CE) separation of free metal ions. To obtain stable metal-Phen chelates during the capillary zone electrophoresis (CZE) run, both pre-column and on-column complexation are required and threefold excess of Phen over metal ions should be added to the sample. The optimized background electrolyte (BGE) consists of 30 mM hydroxylamine hydrochloride and 0.1% methanol at pH 3.6. Under hydrodynamic sampling, CE run at + 20 kV in 65 cm x 0.05 mm ID fused-silica column with detection at 265 nm, baseline separation, satisfactory working ranges (10 microg/L to 5.5 mg/L), sensitive detection limits (1-3 microg/L), good repeatability for migration times (relative standard deviation, RSD 0.36-0.81%, n = 5), peak area (RSD 3.2-4.2%, n = 5) and peak height (RSD 3.2-4.5%, n = 5) were obtained for the metal cations investigated. The reliability of the method was established by parallel determination using the inductively coupled plasma-atomic emission spectrometry (ICP-AES) method giving results within statistical variation. The procedure developed is shown to provide a quick, sensitive, precise, and economic method for simultaneous determination of metal cations that can form stable chelates with Phen.     

Determination of trace metals in high purity gold

The possibility of using ETAAS or ICP-AES for the determination of trace amounts of Ag, Bi, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Pd, Pt and Sb in pure gold is investigated. The influence of the matrix element on the atomization of the trace analytes is studied and optimal instrumental parameters are defined. An analytical method based on matrix element reductive separation followed by spectrometric determination of trace analytes is proposed as an alternative for the analysis of high purity gold. Advantages and disadvantages of proposed analytical procedures from the viewpoint of achieved repeatability, reproducibility and detection limits and of the duration of analysis are discussed. Received: 16 August 1999 / Revised: 23 November 1999 / Accepted: 27 November 1999     

Determination of trace metals in high purity gold

The possibility of using ETAAS or ICP-AES for the determination of trace amounts of Ag, Bi, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Pd, Pt and Sb in pure gold is investigated. The influence of the matrix element on the atomization of the trace analytes is studied and optimal instrumental parameters are defined. An analytical method based on matrix element reductive separation followed by spectrometric determination of trace analytes is proposed as an alternative for the analysis of high purity gold. Advantages and disadvantages of proposed analytical procedures from the viewpoint of achieved repeatability, reproducibility and detection limits and of the duration of analysis are discussed.     

Determination of trace metals in hydrothermal calcites by ICP-methods

Lanthanum, cerium, and europium in calcites from carbonate-sulfide banded ores were determined by standard addition using inductively coupled plasma mass spectrometry (ICP-MS). The concentration ranges in solution were for La 700-36 ng/g, Ce 2000-149 ng/g, and for Eu 140-2.4 ng/g. Only Ce was determined by both ICP methods, and the results agree within 3 to 4%. In a second step, a scan over the mass range of the rare earth elements (REE) was performed. The solutions were analyzed directly without applying preconcentration or separation procedures. ICP atomic emission spectrometry (AES) was used to determine Ca, Mn, and Fe. The matrix Ca is present in a concentration range from 1600 to 1300 g/g and the major impurities Mn and Fe are 152-32 and 100-28 g/g, respectively. The detection limits of ICP-MS for REE are found to be better by two orders of magnitude than for ICP-AES. A commercially available SCIEX Elan ICP-MS with additional software was used to make mathematical corrections for isobaric interferences and molecular ions.Presented in part at the 1989 European Winter Conference on Plasma Spectrochemistry, Reutte, Austria     

Determination of trace elements in iron by neutron-activation techniques

A systematic analytical procedure for the determination of some trace impurities in iron matrices was developed by employing both direct and destructive neutron-activation techniques. Irradiations in fast neutron fluxes, selective activation by epithermal neutrons and coincidence γ-spectrometry measurements were used in some cases, in order to improve the sensitivity for non-destructive analysis; for destructive methods, radiochemical separations based on ion exchange and solvent extraction were applied. Procedures are described, and some results of the determination of low concentrations of Al, Mn, Ti, V (non-destructive), P, S, Zn (destructive) and As, Co, Cr, Cu, Mo, Ni, Sc, W (both methods) in iron are reported and discussed.     

石墨炉原子吸收法测定高纯硒中痕量铁

研究了石墨炉原子吸收直接进样法和石墨炉内富集法测定高纯硒中痕量铁的条件,建立了石墨炉原子吸收法直接测定高纯硒中痕量铁的分析方法.直接进样法的检出限为0.008 μg/g,石墨炉内富集法的检出限为0.004 μg/g,相对标准偏差分别为:5.2%和4.6%,两种方法检测样品结果基本一致.测定含铁0.3 μg/g的高纯硒,测定值的RSD为4.6～5.2%.     

Determination of trace metals in water using x-ray fluorescence spectrometry

A simple, rapid and accurate method for water analysis is proposed. The analytical procedure for the determination of Fe, Mn, Zn, Cu, Cd, As, Pb and Se in water in concentrations as low as a few ppM involves precipitation with a carrier of the metals by diethyldithiocarbamate (DDTC) or 1-(2-pyridylazo)-2-naphthol (PAN) and filitration through a Millipore filter. The precipitates collected on the filter disc are examined by X-ray fluorescence analysis. PAN is excellent for the determination of several metal ions at the ppM level, and DDTC can be used with tartrate as a masking agent if water samples contain large amounts of iron(III).     

Determination of particle-bound trace metals in high purity hydrogen chloride

Summary Two analytical procedures for the determination of particle-bound trace metals in high purity hydrogen chloride are described. Polycarbonate membrane filters with a pore diameter of 0.05 m were used for sampling. Membrane filtration with subsequent instrumental neutron activation analysis (using irradiation with a thermal neutron flux of 10¹³ n cm^–2 s^–1 and irradiation and measurement times of either 20 min) has made it possible to determine the elements Br, Mg, Mn, Na, Sb, Sn, Te, Ti and Zn. For a gas sample volume of 500 l the detection limits determined are in the range of 0.86 ng l^–1 for Zn to 0.30 pg l^–1 for Mn.The elements Cr, Cu, Fe, Mn and Ni were determined by membrane filtration with subsequent graphite tube furnace atomic absorption spectrometry. In this case the detection limits achieved are (for a gas sample volume of 500 l and 4 ml digestion solution) between 8.4 pg l^–1 for Fe and 2.1 pg l^–1 for Cu. The analytical procedures were applied for the characterisation of high purity hydrogen chloride, which is used in the manufacture of highly integrated semiconductor components, by trace analysis, both directly on the gas cylinder and at the 'point of use after passing through the supply system. A review of the status of element determination in high purity process gases is given.

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Bestimmung von partikelgebundenen Metallspuren in hochreinem Chlorwasserstoff

     

Determination of trace amounts of iron by catalytic-adsorptive stripping voltammetry

A highly sensitive and selective voltammetric procedure is described for the determination of trace amounts of iron. The procedure is based on the adsorptive collection of an iron-thiocyanate-nitric oxide complex on a hanging mercury drop electrode. The adsorbed complex catalyzes the reduction of nitrite in solution, which gives a detection limit of 40 ppt iron (30 s accumulation). The stripping current increases linearly with iron concentration up to 80 ppb. The relative standard deviations are 4.2% and 1.6% at 0.5 ppb and 40 ppb respectively. Most of the common ions, except cobalt, do not interfere with the determination of iron. The procedure is applied to determine iron in biological samples, natural waters and analytical-grade chemicals.     

Determination of trace metals in sodium by electro-thermal atomic absorption spectrometry

Graphite-furnace atomic absorption spectrometry is used to analyze sodium metal after conversion to sodium nitrate. Chromium, Ni, Co, Cd and Pb have detection limits in sodium of 0.18, 0.48, 0.11, 0.02 and 0.48 μg g^-1; these are similar to the concentrations in nuclear-grade sodium, except for lead, which is below the detection limit. The behaviour of sodium nitrate, chloride and sulphate as matrices is compared.     

Determination of trace metals in rain water by differential-pulse stripping voltammetry

Differential-pulse stripping voltammetry is applied to measure zinc, cadmium, lead and copper by anodic stripping and selenium(IV) by cathodic stripping in rain water at pH 2; subsequently, at pH 9,1, manganese is measured by anodic stripping on the same portion, and cobalt and nickel are measured in the adsorptive mode after formation of their dimethylglyoximates. The instrumental parameters are optimized. The linear ranges, mutual interferences and detection limits are studied. Excellent accuracy is demonstrated; the standard deviation is around 15% at 2.5–50 μg l^?1 levels. The method is shown to be applicable for rain water.     

Chemical speciation of trace metals in seawater: a review.

The recent development of the chemical speciation of trace metals in seawater is described. The speciation studies reveal that metal ion complexation is one of the most important processes in seawater; especially, most bioactive trace metals, such as Fe(III) and Cu, exist as complexes with ligands in dissolved organic matter. The organic ligands in seawater are characterized with metal ions selected by the HSAB concept. A strong organic ligand, which originates from marine microorganisms, is classified as a hard base including carboxylates. The free organic ligand concentrations in seawater are buffered by complexation with excess amounts of Ca and Mg in seawater. The chemical equilibrium model suggested that the concentrations of bioactive free metal ions are at an optimal level to activities of marine microorganisms. For chemical speciation, it is important to have a better understanding of the ecological roles of trace metals in seawater.     

双波长双指示剂催化动力学光度法测定痕量铁

铁是人体健康所必须的微量元素,它对人体的生理功能有一定影响.如果体内可利用的铁不能满足血红蛋白正常合成的需要,致使红细胞增殖能力下降,就会造成缺铁性贫血.相反,体内铁含量过高,又易产生癌症~([1]).     

Determination of trace metals by neutron activation after coprecipitation with lead phosphate

Lead phosphate quantitatively coprecipitates trace amounts of Ag(I), Cd(II), Cr(III), Cu(II), Mn(II), Th(IV), U(VI) and Zr(IV). The trace elements are determined in the precipitate by instrumental neutron activation analysis (INAA); detection limits are given. The practical application to the determination of U and Th is described.     

Determination of trace metals in estuarine sediments by graphite-furnace atomic absorption spectrometry

A simple and rapid acid digestion method for the decomposition of estuarine sediments is described. Quantitative recovery of Cd, Pb, Cu, Ni, Co, Be and Co is demonstrated. Sensitive, precise and accurate determination of these trace metals by graphite-furnace atomic absorption spectrometry in combination with the L'vov Platform provides an interference-free technique that permits calibration with simple aqueous solutions of metal standards. The accuracy of the method has been confirmed by analysis of two marine sediment reference materials, MESS-1 and BCSS-1.     

Determination of trace impurities in high-purity iron using salting-out of polyoxyethylene-type surfactants

To an iron sample solution was added polyoxyethylene-4-isononylphenoxy ether (PONPE, nonionic surfactant, average number of ethylene oxides 7.5) and the surfactant was aggregated by the addition of lithium chloride. The iron(III) matrix was collected into the condensed surfactant phase in >99.9% yields, leaving trace metals [e.g., Ti(IV), Cr(III), Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Pb(II), and Bi(III)] in the aqueous phase. After removing the surfactant phase by centrifugation, the remaining trace metals were concentrated onto an iminodiacetic acid-type chelating resin. The trace metals were desorbed with dilute nitric acid for the determination by inductively coupled plasma-mass spectrometry or graphite-furnace atomic absorption spectrometry. The proposed separation method allowed the analysis of high-purity iron metals for trace impurities at low μg g⁻¹ to ng g⁻¹ levels.     

Analytical fractionation of trace metals in human serum by means of a chelating ion-exchanger

Conclusions Both, in labile form bound trace metals as well as ionic ones in human serum can selectively be separated on the heavy-metal chelating cellulose HYPHAN under physiological conditions. From the separation kinetics, detailed informations on the binding stability of metal-proteins [e.g., Cu(II), Fe(III), Zn(II)] result. Owing to low blanks, the separation procedure can also be applied to the fractionation of nanogram amounts of other metals [e.g., Al(III), Be(II), Mn(II), Ni(II), Pb(II)] in serum. Furthermore, the coupling with a protein fractionation method (e.g., gelchromatography, isotachophoresis) allows to investigate the binding stability of isolated metal-proteins.

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Analytische Fraktionierung von Schwermetallspuren in Blutserum mittels Chelat-Ionenaustauscher