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  • 1975-1979  (3)
  • Analytical Chemistry and Spectroscopy  (2)
  • Best. von Quecksilber  (1)
  • Cell & Developmental Biology
  • 1
    ISSN: 1618-2650
    Keywords: Best. von Quecksilber ; Spektrometrie, Emission/Spektralphotometrie, MIP-Technik ; Atomabsorption, flammenlos ; Kalt-Dampf-Technik ; systematische Fehler
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Systematische Fehler, die bei der Bestimmung von Hg im ng/g und pg/g-Bereich vor allem bei der Probennahme, Probenvorbereitung und beim Probenaufschluß auftreten, wurden mit 203Hg Radiotracertechniken und mit zwei für den Spurenbereich entwickelten Verbundverfahren untersucht. Beim emissionsspektrometrischen Verfahren (OES-MIP) wird die Probe im mikrowelleninduzierten Sauerstoff Plasma (MIP) verascht und das Hg nach Abtrennung mit einem Au-Absorber in einem Argon-Plasma angeregt. Das emittierte Hg-Licht wird mit einer Photodiode registriert. Nachweisgrenze: 0,01 ng Hg; Variationskoeffizient: 5% für 1 ng Hg. Beim zweiten Verfahren wird Hg nach dem Probenaufschluß (HClO3/HNO3) mit einem mechanisierten Aufschlußsystem nach der Kalt-Dampf-Technik (Ascorbinsäure/SnCl2 bzw. NaBH4) freigesetzt, an einem Gold-Absorber gesammelt und anschließend durch flammenlose AAS bei 253,7 nm bestimmt. Nachweisgrenze: 0,5 ng Hg; Variationskoeffizient: 5% für 5 ng Hg.
    Notes: Summary In the determination of Hg at ng/g and pg/g levels systematic errors are due to faults in the analytical methods such as intake, preparation and decomposition of a sample. The sources of these errors have been studied both with 203Hg-radiotracer techniques and two multi-stage procedures developed for the determination of trace levels. The emission spectrometric (OES-MIP) procedure includes incineration of the sample in a microwave induced oxygen plasma (MIP), the isolation and enrichment on a gold absorbent and its excitation in an argon plasma (MIP). The emitted Hg-radiation (253,7 nm) is evaluated photometrically with a semiconductor element. The detection limit of the OES-MIP procedure was found to be 0,01 ng, the coefficient of variation 5% for 1 ng Hg. The second procedure combines a semi-automated wet digestion method (HClO3/HNO3) with a reduction-aeration (ascorbic acid/SnCl2), and the flameless atomic absorption technique (253,7 nm). The detection limit of this procedure was found to be 0,5 ng, the coefficient of variation 5% for 5 ng Hg.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1979), S. 414-414 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 70 eV mass spectrum of phenyl ω-dimethoxyethyl telluride [C6H5—Te—CH2CH(OR)2, R=CH3]contains an intense peak at m/z 238 which corresponds to a rearrangement ion [C6H5—Te—OR]+. The formation of this species is further illustrated by the presence of a peak at m/z 241 in the spectrum of the hexadeuterated analog (R=CD3) and a peak at m/z 252 in the spectrum of the ethyl analog (R=CH2CH3). These combined results illustrate the presence of only one of the alkoxyl groups in the rearrangement ion. Several other abundant ions that contain oxygen but not tellurium are present in the spectra of these compounds. High resolution analyses have aided in the determination of the origin and composition of several of the characteristic ions formed upon electron impact fragmentation of phenyl ω-dimethoxyethyl telluride.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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