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  • 2000-2004  (2)
  • 1975-1979  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 366 (2000), S. 48-53 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract When mercury is quantified by ICP-MS under routine conditions (external calibration) in reference materials, which require mineralization with nitric acid, the experimental concentrations are almost always unacceptably low in comparison to certified values. Sorption of mercury on the Teflon surfaces of the digestion vessels, changes in the viscosity of the aspirated solutions, in the efficiency of the nebulization, in the aerosol transport, and memory effects cannot be responsible for the low results. The intensity of a mercury signal is strongly dependent on the concentration of nitric acid (and other mineral acids) in the measured solutions. Correct results for mercury in the SRM GBW-90101 (Chinese human hair; 2.16 ± 0.21 mg Hg/kg certified) can only be obtained, when the solutions, with which the external calibration curves were established, have exactly the same nitric acid concentration as the aspirated digests (2.03 ± 0.01 mg Hg/kg; n = 5), when mercury is determined by the standard addition method (2.10 ± 0.01 mg Hg/kg; n = 5), or when the experimental mercury concentration obtained at a nitric acid concentration in the digest, different from the concentration in the external calibration solutions, is corrected mathematically based on a pre-established function [Hg2+] = f [HNO3]. The concentrations found by this mathematically based correction 2.04 ± 0.01 mg Hg/kg (n = 5) is in good agreement with the values obtained by acid matched calibration or by the standard addition method. For practical work with large numbers of samples the mathematical correction appears to be the method of choice. For occasional mercury determinations, the standard addition method seems to be the most practicable.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A microwave procedure for the digestion of the NIST 1634b reference material “residual fuel oil” in closed pressurized vessels was developed in an attempt to facilitate routine analysis and obtain reproducible conditions or comparable results. The influence of sample size, reagent composition and volume, microwave power, and duration of heating on the digestion procedure was studied. Pressure and temperature inside the reaction vessels were monitored to determine the progression of the reaction and to develop optimal conditions. A nine-step heating program requiring 36.5 min with microwave power not exceeding 450 W in the pulsed mode was found suitable for the digestion of ∼ 250 mg fuel oil with a mixture of nitric acid (5.0 mL) and hydrogen peroxide (2.0 mL). The reproducibility of microwave power was determined in terms of the relative standard deviations (n = 3) for temperature (2.7%) and pressure (4.9%) data. The vapor pressures obtained with 5.0 mL Milli-Q water (heated) in an 80-mL digestion vessel showed good agreement with literature data. The excess acid in the resulting digests was removed by evaporation and the concentrations of 24 elements (Ag, Al, As, Ba, Bi, Ca, Cd, Co, Cr, Cu, Fe, Hg, Mg, Mo, Ni, Pb, Sb, Sn, Sr, Ti, Tl, V, U, and Zn) were determined in the diluted digests by inductively coupled plasma mass spectrometry (ICP-MS). The experimental results were in good agreement with the certified and recommended concentrations for eight elements (Al, As, Co, Cr, Ni, Pb, V, Zn) in solutions obtained after one digestion step. An additional digestion step, consisting of intermediate cooling and venting stages, was required for the accurate determination of Fe. No agreement was reached for Ca and Ba even after two-step digestion. The proposed method of digestion provided precise results with relative standard deviations generally less than 5% for most of the elements determined.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 640-643 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of several alkyl phenyl tellurides, C6H5TeR (R = CH3, CD3, C2H5, n-C3H7, i-C3H7 and n-C4H9) have been studied with special emphasis on the fragmentation patterns involving cleavage of the alkyl and aryl tellurium-carbon bonds. Each compound exhibited intense parent ions. The rearrangement ions [C6H6Te]+⋅ and [C6H6]+⋅ were found in the spectra of phenyl ethyl and higher tellurides. Two other rearrangement ions [HTe]+ and [C7H7]+ were observed in the spectrum of each compound. Examination of the mass spectrum of phenyl methyl-d3 telluride demonstrated that the [HTe]+ ions derive hydrogen from the phenyl group.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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