TY - BOOK
T1 - Solid-phase microextraction.
T2 - Development and validation of new analytical methods.
AU - Nilsson, Torben
PY - 1997
Y1 - 1997
N2 - The objective of this study has been to develop new analytical
methods using the rapid, simple and solvent-free extraction
technique solid-phase microextraction (SPME) for the quantitative
analysis of organic pollutants at trace level in drinking water
and environmental samples. The dynamics of SPME were examined for
halogenated and non-halogenated volatile hydrocarbons, and a
standard method for their quantitative analysis in aqueous samples
was developed and validated in inter-laboratory studies on the
basis of reference material and in comparison with the traditional
methods. The influences of some possible interferences on the SPME
process were examined, and new SPME probes were tested for the in
situ monitoring of groundwater pollutants. Inter-laboratory
studies were carried out also for the validation of SPME for the
quantitative analysis of organochlorine, organonitrogen and
organophosphate pesticides and triazine herbicides together with
their metabolites in aqueous samples. SPME combined with gas
chromatography proved to be a precise, accurate and sensitive
technique for water analysis. Also SPME combined with high
performance liquid chromatography was tested, and a method for the
combined analysis of four classes of polar herbicides was
developed. Throughout the studies with aqueous samples the main
purpose has been to evaluate and optimise the quantitative aspects
of the SPME analysis. With calibration by standard addition also
the quantitative analysis of soil samples by SPME was feasible in
spite of the strong matrix effects. Finally, SPME was applied to
flavour analysis and two new methodologies were established for
the classification of microbiological fungi.
AB - The objective of this study has been to develop new analytical
methods using the rapid, simple and solvent-free extraction
technique solid-phase microextraction (SPME) for the quantitative
analysis of organic pollutants at trace level in drinking water
and environmental samples. The dynamics of SPME were examined for
halogenated and non-halogenated volatile hydrocarbons, and a
standard method for their quantitative analysis in aqueous samples
was developed and validated in inter-laboratory studies on the
basis of reference material and in comparison with the traditional
methods. The influences of some possible interferences on the SPME
process were examined, and new SPME probes were tested for the in
situ monitoring of groundwater pollutants. Inter-laboratory
studies were carried out also for the validation of SPME for the
quantitative analysis of organochlorine, organonitrogen and
organophosphate pesticides and triazine herbicides together with
their metabolites in aqueous samples. SPME combined with gas
chromatography proved to be a precise, accurate and sensitive
technique for water analysis. Also SPME combined with high
performance liquid chromatography was tested, and a method for the
combined analysis of four classes of polar herbicides was
developed. Throughout the studies with aqueous samples the main
purpose has been to evaluate and optimise the quantitative aspects
of the SPME analysis. With calibration by standard addition also
the quantitative analysis of soil samples by SPME was feasible in
spite of the strong matrix effects. Finally, SPME was applied to
flavour analysis and two new methodologies were established for
the classification of microbiological fungi.
M3 - Book
BT - Solid-phase microextraction.
PB - Technical University of Denmark
CY - Lyngby
ER -