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 15,165 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The analysis of trace elements in biological samples will extend our understanding of the impact that environmental exposure to these elements has on human health. Measuring arsenic content in nails has proven useful in studies evaluating the chronic body burden of arsenic. In this study, we developed methodology with inductively coupled plasma-mass spectrometry (ICP-MS) for the determination of total arsenic in nails. We assessed the utility of the washing procedures for removing surface contamination. Four types of preanalysis treatments (water bath, sonication, water bath plus sonication, and control) after sample decomposition by nitric acid were compared to evaluate the digestion efficiencies. In addition, we studied the stability of the solution over 1 wk and the effect of acidity on the arsenic signal. Arsenic content in the digested solution was analyzed by using Ar-N2 plasma with Te as the internal standard. The results suggest that washing once with 1% Triton X-100 for 20 min for cleaning nail samples prior to ICP-MS analysis is satisfactory. Repeated measurement analysis of variance revealed that there was no significant difference among the various sample preparation techniques. Moreover, the measurements were reproducible within 1 wk, and acidity seemed to have no substantial influence on the arsenic signal. A limit of detection (on the basis of three times the standard deviation of the blank measurement) of 7 ng As/g toenail was achieved with this system, and arsenic recoveries from reference materials (human hair and nails) were in good agreement (95-106% recovery) with the certified/reference values of the standard reference materials. ICP-MS offers high accuracy and precision, as well as high-throughput capacity in the analysis of total arsenic in nail samples.
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PMID:Determination of total arsenic concentrations in nails by inductively coupled plasma mass spectrometry. 1007 18

Micro-electrodes were applied to anaerobic granular sludge, which was developed in a UASB reactor, to examine intra-granule profiles with respect to pH, glucose and sulfide. When glucose was employed as a bulk liquid substrate, the micro-electrodes study demonstrated the pH behavior along granule depth: pH decrement at the granule exterior portion due to acid formation (buildup of acidity), and subsequent pH increment at the granule inner portion due to the consumption of acid (buildup of alkalinity). Sulfide micro-electrode proved sulfate reduction that mostly occurred at the granule exterior portion. Chemical equilibrium consideration evidently explained the occurrence of ferric sulfide predominantly in the interior portion, which accounts well for the morphology of a representative double-layered structure of granules grown on a low level of sulfite. Inorganic elements distribution within anaerobic granule was examined by electron probe X-ray micro analysis (EPMA) and ICP methods. The presence of crystalline calcium carbonate (calcite) was identified by X-ray diffraction analysis.
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PMID:Microbial-ecological significance of sulfide precipitation within anaerobic granular sludge revealed by micro-electrodes study. 1154 62

An investigation on the complex formation equilibria between divalent metal ions Me (with Me=Mn, Co, Ni, Cu, Cd, and Pb) and phytic acid (H(12)L) is presented. Experiments were performed through a potentiometric methodology by measuring, at 25 degrees C, the proton and, in some cases (Cu(2+), Cd(2+), and Pb(2+)), also the metal ion activity at equilibrium in solutions containing, besides the metal and the ligand, 3 M NaClO(4) as the ionic medium. Unhydrolyzed solutions of the metal ion at millimolar concentration levels were titrated with solutions of about 10 mM sodium phytate, until the formation of a solid phase took place (always at pH approximately 2.5, except in the case of Cu(2+), which formed soluble complexes up to pH approximately 3.3). Coulometry was employed to produce very dilute solutions of either Cu(2+), Cd(2+), or Pb(2+) of accurately known composition. The emf data were explained by assuming, in the acidity interval explored, the formation of the complexes of general stoichiometry MeH(5)L(5-) and Me(2)H(3)L(5-). Coordination compounds in the solid state were also synthesized and characterized by elemental analysis, thermal analysis, and ICP spectroscopy. The solids had a general stoichiometry Me(6)H (t)LCl (t). x H(2)O, with the following t and x values for each metal investigated: Me ( t; x) = Mn (4; 2); Co (4; 2); Ni (4; 2); Cu (2; 2.5); Zn (2; 1); Sn (6; 6).
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PMID:Complex formation between phytic acid and divalent metal ions: a solution equilibria and solid state investigation. 1220 61

Tin is considered to be a priority contaminant by the Codex Alimentarius Commission. Tin can enter foods either from natural sources, environmental pollution, packaging material or pesticides. Higher concentrations are found in processed food and canned foods. Dissolution of the tinplate depends on the of food matrix, acidity, presence of oxidising reagents (anthocyanin, nitrate, iron and copper) presence of air (oxygen) in the headspace, time and storage temperature. To reduce corrosion and dissolution of tin, nowadays cans are usually lacquered, which gives a marked reduction of tin migration into the food product. Due to the lack of modern validated published methods for food products, an ICP-AES (Inductively coupled plasma-atomic emission spectroscopy) method has been developed and evaluated. This technique is available in many laboratories in the food industry and is more sensitive than atomic absorption. Conditions of sample preparation and spectroscopic parameters for tin measurement by axial ICP-AES were investigated for their ruggedness. Two methods of preparation involving high-pressure ashing or microwave digestion in volumetric flasks were evaluated. They gave complete recovery of tin with similar accuracy and precision. Recoveries of tin from spiked products with two levels of tin were in the range 99+/-5%. Robust relative repeatabilities and intermediate reproducibilities were <5% for different food matrices containing >30 mg/kg of tin. Internal standard correction (indium or strontium) did not improve the method performance. Three emission lines for tin were tested (189.927, 283.998 and 235.485 nm) but only 189.927 nm was found to be robust enough with respect to interferences, especially at low tin concentrations. The LOQ (limit of quantification) was around 0.8 mg/kg at 189.927 nm. A survey of tin content in a range of canned foods is given.
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PMID:Determination of total tin in canned food using inductively coupled plasma atomic emission spectroscopy. 1232 43

Trace metal composition of winter snowpack, snow-melt filter residues and top-soil samples were determined along three transects through industrial towns in the Usa basin, North-East Russia: Inta, Usinsk and Vorkuta. Snow was analysed for Ag, Al, As, Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr and Zn using ICP-MS (Ca and K by F-AAS for Vorkuta only), pH and acidity/alkalinity. Filter residues were analysed for: Al, Ba, Ca, Cd, Cu, K, Mg, Mn, Ni, Pb, Sr and Zn using F-AAS and GF-AAS; top-soil samples were analysed for Ba, Cu, Mg, Mn, Na, Ni, Pb, Sr, Zn using F-AAS. Results indicate elevated concentrations of elements associated with alkaline combustion ash around the coal mining towns of Vorkuta and Inta. There is little evidence of deposition around the gas and oil town of Usinsk. Atmospheric deposition in the vicinity of Vorkuta, and to a lesser extent Inta, added significantly to the soil contaminant loading as a result of ash fallout. Acid deposition was associated with pristine areas whereas alkaline combustion ash near to emission sources more than compensated for the acidity caused by SO2.
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PMID:Anthropogenic metal enrichment of snow and soil in north-eastern European Russia. 1247 56

A new method for determining iodine had been developed in ICP-AES. An oxidant, NaNO2 and a sample containing iodine ion were mixed in the PHD hydroid generation device, the producing iodine molecules were nebulized in nebulizer and then the iodine gas came into troch directly. The problem that the intensity of iodine decreases with the increase of time was solved. It was found that NaNO2 decreased the effect of Cl- in the low acidity. A detection limit of 14 ng.mL-1 was obtained and the RSD of the measurement for 2 micrograms.mL-1 of iodine was 1.2% (n = 10). The average recoveries of iodine were 99.44%. The method was applied to the determination of salt and seawater.
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PMID:[Study on the determination of iodine by inductively coupled plasma atomic emission spectrometry]. 1294 71

The content of K, Na, Ca, Mg, Fe in electrolytic manganese are determined by FAAS, and content of Cu, Cr, Co, Ni determined by GFAAS after sample is dissolved by HCl (aq). The best condition for determination is investigated, including method of dissolving and acidity, and influence of coexist elements and exclusion of these influences. The methods prove to be rapid, accurate and convenient. The recoveries of method are 88.9%-108.7%, the relative standard deviations are 0.6%-6.7%. The results obtained by calibration curve method are in good conformity with the standard addition method and results measured by ICP. The method can be utilized in analysis of impurities in electrolytic manganese.
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PMID:[Determination of impurities in electrolytic manganese by atomic absorption spectrometry]. 1295 17

ICP-AES was used for the direct determination of 15 rare earth elements in synthetic solutions and real sample. Spectral interferences between REEs in the mixtures of rare earth were investigated with a high-resolution echelle spectrometer and suitable analytical lines of 15 rare earth elements were selected. The Multicomponent Spectral Fitting(MSF) models were made. The method was used to remove spectral interferences and background. The factors influence the modes were discussed. The influences of acidity and ICP parameters were investigated. The compromise condition of simultaneous determination of 15 REEs was selected. Axially viewed ICP torch was used to determine 15 REEs, The detection limits are Y 0.21 microgram.L-1, La 9.1 micrograms.L-1, Ce 14.1 micrograms.L-1, Pr 1.9 micrograms.L-1, Nd 7.8 micrograms.L-1, Tm 0.37 microgram.L-1, Yb 0.12, Lu microgram.L-1, Ho 0.06 microgram.L-1, Er 0.06 microgram.L-1, Tb 0.53 microgram.L-1, Sm 1.14 micrograms.L-1, Eu 0.09 microgram.L-1, Dy 0.08 microgram.L-1, Gd 0.30 microgram.L-1. The recoveries of this procedure are between 98.4% and 101.7%. The RSD is within 2%. The method is rapid and accuracy.
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PMID:[Direct determination of rare earth elements in rare earth chloride and light rare earth oxide by ICP-AES]. 1295 56

A method for the determination of Au, Pt, Pd and Rh by ICP-AES after preconcentration on a column containing diphenylthiourea immobilized on aluminum oxide was developed. The optimum acidity of solution, amount of adsorbent, elution solution, flow rate and volume of the samples were obtained for the elements studied. The effect of interfering ions on the recovery of the analytes was also investigated. Under the optimum measuring conditions, the recoveries were found to be between 95%-105%. The detection limits of Au, Pd, Pt and Rh was 0.0085, 0.022, 0.015 and 0.022 microgram.g-1, respectively, and the relative standard deviation was lower than 5%. This procedure was applied to the determination of Au, Pd, Pt and Rh in geological samples.
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PMID:[Determination of trace platinum, palladium, gold and rhodium in geological samples by ICP-AES after preconcentration by diphenlthiourea immobilized on aluminum oxide]. 1296 97

Analysis of Acer pseudoplatanus L. (sycamore) tree rings using ICP-MS was used to assess the impact of metal deposition on trees growing in the vicinity of a metal refinery at Prescot, north-west England compared to a reference site at Croxteth 6 km distant receiving minimal deposition. No difference in tree growth between sites was recorded. Large reductions in Cu and Cd deposition since the late 1970s was accompanied by a steep decline in Cd concentrations in the outer rings in trees close to the refinery. A similar reduction in Cu concentrations was less apparent due to a tendency for Cu to increase in the outer rings. Zinc and Ni were higher in xylem at Prescot compared to Croxteth. There was no trend in Zn concentrations at either site although Ni concentrations increased in trees close to the refinery after 1982. Manganese concentrations in xylem were much higher at Prescot; Mn levels declined until the late 1970s and then increased slightly in later years interspersed by large concentration peaks within individual years during the 1980s. There was little change in Mn concentrations in trees at Croxteth during this period. Calcium, Mg and Sr concentrations remained steady or declined slightly in rings formed since 1965 in trees at Croxteth. Concentrations of Ca, Mg and Sr were higher in rings formed prior to the mid 1970s in trees at Prescot, but declined steadily after this period, although peaks in concentrations of each element were recorded in individual years during the 1980s. Phosphorous concentrations in rings increased towards the cambium at Croxteth, although P levels decreased in rings formed after 1982 at Prescot. No difference in K concentrations between sites was recorded. Lead concentrations in xylem at both sites declined steadily in rings formed after 1970, although concentrations were higher at the reference site. Analysis of individual sycamore tree rings appears to record short-term changes in pollution episodes, with little lateral movement of elements occurring. It is suggested that changes in element concentrations in trees close to the refinery are a result of reduced metal deposition combined with increased soil acidity due to reduced buffering capacity of metal ions in rainfall.
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PMID:Analysis of tree rings using inductively coupled plasma mass spectrometry to record fluctuations in a metal pollution episode. 1509 73


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