Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Adsorption of fenitrothion and 3-methyl-4-nitrophenol on soils and sediment (1983)
    Springer
    Bulletin of environmental contamination and toxicology 30 (1983), S. 621-627 
    Details
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Notes: Conclusions It was found that fenitrothion and its hydrolysis product 3-methyl-4-nitrophenol are adsorbed on sediment and soils in amounts that increase with increasing organic matter content of the adsorbate. Whereas the use of K-values derived from the Freundlich equation (Eq. 1) has limitations, the use of a modified Freundlich equation presents problems when the slope of the isotherm is appreciably larger than unity. Both compounds can be adsorbed on soils so as to reach concentrations that are fungitoxic on agar plates. Since compounds adsorbed on soil (and on the organic litter of the forest floor) would not be readily subject to photodegradation, the results of this study show that it is essential that attention be given to further studies on the microbial degradation of these compounds.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01610184
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    The mass spectra of 3-substituted furans (1972)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 367-372 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A fragmentation pattern characteristic of 3-substituted furans, in which the 3-substituent carries an oxygen function, is discussed. Examination of the spectra of some meliacins, as well as those of some synthetic model compounds, illustrates the diagnostic value of this particular fragmentation. In addition the spectrum of methyl limonilate (III, R = CH3) is discussed in some detail.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210060403
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...