Library

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
Filter
  • 1990-1994  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Water and environment journal 5 (1991), S. 0 
    ISSN: 1747-6593
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Previous attempts to utilize ion chromatography for the analysis of sea water samples have failed through chronic interference by the major ions (na, Mg, Ca) during the preconcentration stage. As part of ongoing research into ion chromatography, a technique has been developed to overcome these interferences, using a two-stage preconcentration step, prior to separation on a cation-exchange column. This has made it possible to detect μg/l quantities of trace metals in samples containing g/l concentrations of sodium, magnesium and calcium. A modified commercially-available ion chromatographic system was used to analyse copper, nickel, zinc, cobalt and manganese in saline waters. Detection limits were typically less than 1 μg/l, with relative standard deviation of less than 10%. Hence this new method has the potential to provide an inexpensive multi-elemental sea water analysis with the minimum of handling. In addition, the simplicity and sensitivity of the technique may make it suitable for unattended use as a remote monitor of metals.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 109 (1992), S. 27-33 
    ISSN: 1436-5073
    Keywords: arsenic speciation ; water analysis ; hydride ; storage ; hidden arsenic ; photolysis ; interstitial waters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The determination of arsenic species by the trapping of volatile hydrides prior to atomization in the light path of an atomic absorption spectrometer is described and its operation in the measurement of arsenic species in the marine environment are discussed. Examples are drawn from the analysis of Tamar estuary water and sediment interstitial (pore) waters and from studies of the temporal variation of dimethylarsenic in coastal waters. Improvements in both the design and operation of the technique have resulted in enhanced performance. Baseline resolution of inorganic arsenic, monomethylarsenic and dimethylarsenic is now possible and trimethylarsine is resolved. Ultraviolet photolysis of arsenobetaine and arsenocholine gives partial conversion to trimethylarsine oxide. This can be employed in the qualitative appraisal of the presence of trimethylarsenic species. Current detection limits (3 sigma) for inorganic, mono- and di-methylarsenic lie in the range 19 to 61 pg absolute, giving 19–61 ng/1 concentration detection limits for 1 ml samples. This can be improved even further by using larger sample volumes. The properties of the analysis system when presented with various arsenic species are described. A ca. 10% loss of arsenite occurs in samples stored at —20 °C and immediate freezing of samples in liquid nitrogen is recommended.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...