Determination of Cd and Pb in fuel ethanol by filter furnace electrothermal atomic absorption spectrometry

A method was developed for quantification of Cd and Pb in ethanol fuel by filter furnace atomic absorption spectrometry. Filter furnace was used to eliminate the need for chemical modification, to stabilize volatile analytes and to allow the application of short pyrolysis step. The determinations in samples were carried out against calibration solutions prepared in ethanol. Recovery tests were made in seven commercial ethanol fuel samples with values between 90 and 120%. Limits of detection were 0.1 µg L-1 for Cd and 0.3 µg L-1 for Pb. Certified water samples (APS 1071, APS 1033, NIST 1643d, NIST 1640) were also used to evaluate accuracy and recoveries from 86.8% to115% were obtained

The use of electrothermal vaporizer coupled to the inductively coupled plasma mass spectrometry for the determination of arsenic, selenium and transition metals in biological samples treated with formic acid

A fast method for the determination of As, Co, Cu, Fe, Mn, Ni, Se and V in biological samples by ETV-ICP-MS, after a simple sample treatment with formic acid, is proposed. Approximately 75mg of each sample is mixed with 5mL of formic acid, kept at 90°C for 1h and then diluted with nitric acid aqueous solution to a 5% (v/v) formic acid and 1% (v/v) nitric acid final concentrations. A palladium solution was used as a chemical modifier. The instrumental conditions, such as carrier gas flow rate, RF power, pyrolysis and vaporization temperatures and argon internal flow rate during vaporization were optimized. The formic acid causes a slight decrease of the analytes signal intensities, but does not increase the signal of the mainly polyatomic ions ( 14N 35Cl +, 14N 12C +, 40Ar 12C +, 13C 37Cl +, 40Ar 36Ar +, 40Ar 35Cl +, 35Cl 16O +, 40Ar 18O +) that affect the analytes signals. The effect of charge transfer reactions, that could increase the ionization efficiency of some elements with high ionization potentials was not observed due to the elimination of most of the organic compounds during the pyrolysis step. External calibration with aqueous standard solutions containing 5% (v/v) formic acid allows the simultaneous determination of all analytes with high accuracy. The detection limits in the samples were between 0.01 (Co) and 850μgkg -1 (Fe and Se) and the precision expressed by the relative standard deviations (RSD) were between 0.1% (Mn) and 10% (Ni). Accuracy was validated by the analysis of four certified reference biological materials of animal tissues (lobster hepatopancreas, dogfish muscle, oyster tissue and bovine liver). The recommended procedure avoids plasma instability, carbon deposit on the cones and does not require sample digestion. © 2011 Elsevier B.V..Fil: Tormen, Luciano. Universidade Federal Da Fronteira Sul; Brasil. Universidade Federal de Santa Catarina; BrasilFil: Gil, Raul Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Frescura, Vera L. A.. Universidade Federal de Santa Catarina; BrasilFil: Martinez, Luis Dante. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Curtius, Adilson J.. Universidade Federal de Santa Catarina; Brasi

Total Mercury Determination in Petroleum Green Coke and Oily Sludge Samples by Cold Vapor Atomic Fluorescence Spectrometry

A fast, simple and reliable method for Hg determination in green coke and oily sludge samples by atomic fluorescence spectrometry is described. Microwave digestion and extraction procedures were evaluated for highly complex samples of coke and oily sludge. The concentrations of SnCl2 and HCl to promote Hg vapor, were optimized, as well as the concentration of KMnO4, to stabilize the Hg2+ before the atomic vapor formation. Accuracy of the method was evaluated through certified reference material, for green coke, and comparison with cold vapor atomic absorption spectrometry (CV AAS), for oily sludge. Recovery tests were also performed. Limits of detection and quantification were 0.8 and 2.6 µg kg−1, respectively. Ten green coke and nine sludge samples were analysed and Hg concentrations in coke are very low, between 0.005 and 0.065 mg kg−1, but oily sludge samples have high concentrations, ranging from 42.5 to 376.6 mg kg−1, requiring careful management

Determination of Rare Earth Elements in Spent Catalyst Samples from Oil Refinery by Dynamic Reaction Cell Inductively Coupled Plasma Mass Spectrometry

The determination of rare earth elements (REE) in spent catalyst samples from oil refinery is proposed. Three sample treatment procedures were tested, one without HF and two using different amounts of HF and boric acid. A microwave evaporation step to promote the dissolution of the REE fluorides was carried out. The medium containing 1.0 mL of HF and 8.0 mL of boric acid promoted the complete digestion. Studies were carried out using a reaction cell to overcome polyatomic interferences on four elements by inductively coupled plasma mass spectrometry (ICP-MS). Certified reference material, TDB-1, was used to evaluate the method accuracy applied to ten spent catalysts. The sample treatment is fast and promotes the complete digestion of the samples and the developed procedure led to proper accuracy for 14 of the 16 determined analytes. Recovery tests presented values between 87% and 101%

A novel approach to cold vapor generation for the determination of mercury in biological samples

A novel approach to the generation of mercury vapor at high pH by the simple addition of NaOH or other base to a solution containing mercury ions is described. Subsequent addition of another reducing agent, such as NaBH4 or SnCl2, is unnecessary. Following total dissolution of sample using HNO3 and H2O2 in a closed microwave vessel, the pH of the sample solution is increased to 13 by the addition of NaOH. After standing for 90 min in a closed vessel, the Hg0 is directed to the plasma by a flow of argon. Emission from mercury is measured at 253.652 nm by an axial view inductively coupled plasma optical emission spectrometer (ICP OES). The procedure was applied to five certified biological samples, yielding a detection limit (3s, n = 10) of 0.04 \ub5g g-1 based on a nominal sample mass of 0.5 g in a final volume of 50 mL. Calibration was achieved using simple aqueous standard solutions containing 0.1 mol L-1 NaOH. The procedure was efficient, with determined values lying in the range of 85-113 % of the certified values, showing good agreement at the 95% confidence level (t-test). The precision was fit for purpose, with relative standard deviations ranging from 7 to 9%. Organomercury species in solution were not detected; only Hg2+ in solution produces a signal. This new procedure provides for a simple approach to quantitation (and potentially speciation).Peer reviewed: YesNRC publication: Ye

EXTRAÇÃO ASSISTIDA POR ULTRASSOM PARA DETERMINAÇÃO COLORIMÉTRICA DE FERRO EM SOLO: UMA COMPARAÇÃO COM ESPECTROMETRIA DE MASSA COM PLASMA INDUTIVAMENTE ACOPLADO

A simple procedure for ultrasound-assisted extraction and colorimetric determination of iron in soil samples was developed. The iron concentration in the analyzed samples was determined by the colorimetric method and the results compared with inductively coupled plasma mass spectrometry (ICP-MS). Fifteen soil samples were analyzed and the iron concentration results compared with those obtained by ICP-MS using microwave-assisted sample digestion. The proposed procedure showed good efficiency for iron extraction and the results obtained by colorimetric determination exhibited good agreement with ICP-MS. Moreover, ultrasound-assisted extraction and colorimetric determination is a simple, fast and low-cost procedure for application in routine analysis