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  • 5-chlorosalicylidene-o-aminophenol  (1)
  • pesticides residues  (1)
  • solid-phase spectrofluorimetry  (1)
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  • 1
    ISSN: 1436-5073
    Schlagwort(e): 5-chlorosalicylidene-o-aminophenol ; indium determination ; spectro-fluorimetry
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A Spectrofluorimetric method for microdetermination of indium, based on the formation of a fluorescent 2∶1 (ligand:metal) complex between In (III) and 5-chlorosalicylidene-o-aminophenol at an apparent pH of 4.70 in an aqueous-ethanol medium (50% v/v ethanol) is proposed. The calibration graph is linear over the range 10.0–80.0 μg/l, the relative standard deviation 2.7% and the detection limit 1.5 μg/l. The method has been applied to the determination of indium in synthetic samples and natural waters.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1573-4994
    Schlagwort(e): Benomyl and morestan determination ; solid-phase spectrofluorimetry ; pesticides residues ; water analysis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract In this paper a new, sensitive, and simple method for simultaneous determination of pesticides morestan and benomyl at trace levels in waters is reported. Both chemicals, showing native fluorescence in solution at neutral medium, were fixed on C-18 silica gel at pH 1, giving a fluorescent system. The benomyl-morestan-silica gel system, after dry, was packed in a 1-mm silica cell and its synchronous fluorescence spectra were recorded at δλ=80 nm for determination of benomyl and δλ=25 nm for determination of morestan. Measurements of fluorescence were performed at λ1=289 nm and λ2=367 nm for benomyl and morestan analysis, respectively. The applicable concentration ranges were from 0.5 to 15.0 ng·ml−1 for benomyl and from 0.6 to 15.0 ng·ml−1 for morestan, with relative standard deviations of 1.2 and 1.5% for benomyl and morestan, respectively, being 0.15 and 0.18 ng·ml−1 its respective detection limits. The method was applied to the simultaneous determination of residues of both pesticides in water of different provenances.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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