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Organic Phosphorus Compounds in Aquatic Sediments : Towards Molecular Identification with Mass Spectrometry

De Brabandere, Heidi, 1980- (författare)
Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
Waldebäck, Monica, Ph.D. (preses)
Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
Rydin, Emil, Ph.D. (preses)
Uppsala universitet,Institutionen för ekologi och evolution
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Sjöberg, Per J. R., Ph.D. (preses)
Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
Danielsson, Rolf, Associate Professor (preses)
Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
Cooper, William T., Professor (opponent)
Analytical and Environmental Chemistry, Dept. of Chemistry and Biochemistry, Florida State University
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 (creator_code:org_t)
ISBN 9789155473068
Uppsala : Universitetsbiblioteket, 2008
Engelska 58 s.
Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1651-6214 ; 560
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • Phosphorus (P) regulates trophic status in most aquatic systems. However, only bioavailable P contributes to primary production. In most lakes and shallow seas, mineralisation of sediment P into its bioavailable form and its release to the water column is important for maintaining primary production. Sediment organic P forms a substantial proportion of this P to be mineralised and can originate from different sources on land (farmland, forests, etc.) or from primary production in the lake. These organic P forms can thus be expected to have differing composition, degradability and recyclable P content. Knowledge of the chemical structure of sediment organic P compounds is scarce, mainly due to lack of appropriate analytical techniques. The commonly used 31P-nuclear magnetic resonance (31P-NMR) technique, only identifies P binding groups, so a mass spectrometric (MS) analysis method was developed that allows individual sediment organic P compounds to be identified. EDTA as pre-extractant resulted in the highest P yield in subsequent NaOH extraction. Extracted organic P compound groups were identified using 31P-NMR. For identification of specific P compounds with MS, a sample preparation method prior to electrospray tandem mass spectrometry (ESI-MS/MS) analysis was developed. Liquid chromatography (LC) with porous graphitic carbon prior to ESI-MS/MS enhanced sensitivity and selectivity, enabling several of the ions detected to be identified as nucleotides. 31P-NMR analysis showed P monoesters to be the most stabile P compounds throughout a lake sediment profile. The developed LC-ESI-MS/MS analysis method revealed that some monoester-P (nucleotides) were labile, while other P compounds increased in concentration with Baltic Sea sediment depth and were therefore considered stabile. Differences in patterns of P compounds detected were also shown depending on catchment characteristics in relation to Baltic Sea sediment age. For cost-effective management of eutrophication, knowledge of the sources of degradable organic P forms, contributing to internal loading, is needed. This thesis showed the developed LC-ESI-MS/MS analysis method to be a powerful analytical tool for this purpose.

Ämnesord

NATURVETENSKAP  -- Kemi -- Analytisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Analytical Chemistry (hsv//eng)

Nyckelord

electrospray ionisation
mass spectrometry
liquid chromatography
organic phosphorus
aquatic sediment
eutrophication
sample preparation
extraction
Analytical chemistry
Analytisk kemi

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