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Microextraction for usage in environmental monitoring and modelling of nitroaromatic compounds and haloanisoles
Örebro universitet, Institutionen för naturvetenskap.
2008 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Processes in the environment are often complex and the description and prediction of the behaviour of environmental pollutants requires sophisticated methodology including multidimensional technology. Multivariate statistical methods including principal component analysis (PCA) and partial least squares projection to latent structures (PLS) were used to characterise several nitroaromatic compounds according to a large number of chemical and physical properties. These descriptors were derived from databases and semi-empirical, empirical and quantum-chemical calculations. A model was calculated and used for prediction of experimentally determined relevant environmental parameters, including volatility through gas chromatographic retention times and the distribution between air and water phase using solid-phase microextraction measurements. Analytical microextraction techniques are very well suited for both monitoring and measuring relevant environmental properties. Two such methods, solid-phase microextraction (SPME) and microextraction by packed syringe (MEPS), which are both faster and less resource demanding than traditional methodology, were used to improve the analysis of nitroaromatic compound and haloanisoles. Both techniques showed few interfering compounds and good reproducibility in combination with GC-MS detection. The reproducibility for SPME and MEPS was further enhanced by the usage of isotopically labelled internal standards (nitroaromatic compounds) or internal standards with similar chemical properties as the analytes (haloanisoles).

The SPME method for nitroaromatic compounds was tested using industrial wastewater from a wastewater treatment facility receiving input from several nitrogen based industries. Using gas chromatography-negative chemical ionisation-mass spectrometry(GC-NCI-MS) as the final detection, limits of detection (LODs) in the range 0.02–38 ng L−1 were achieved. Results for the 2,4,6-TCA (TCA) and 2,4,6-TBA (TBA) using high resolution GC-MS were even more impressive obtaining LODs in the range 0.02-0.03 ng L-1, which are currently the lowest reported in the international literature. Although the newly developed MEPS technology is generally faster than SPME, similar LODs as for SPME could not yet be achieved. Both methods were found to be so sensitive that TCA and TBA could be detected in wine before it could be sensorically noticed as cork tainted.

sted, utgiver, år, opplag, sider
Örebro: Örebro universitet , 2008. , s. 58
Serie
Örebro Studies in Chemistry, ISSN 1651-4270 ; 9
Emneord [en]
PCA, PLS, QSPR, SPME, MEPS, nitroaromatic compounds, TCA, TBA
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
URN: urn:nbn:se:oru:diva-1786ISBN: 978-91-7668-582-2 (tryckt)OAI: oai:DiVA.org:oru-1786DiVA, id: diva2:135475
Disputas
2008-03-07, Bion, Forumhuset, Örebro universitet, Örebro, 10:00
Opponent
Veileder
Tilgjengelig fra: 2008-02-15 Laget: 2008-02-15 Sist oppdatert: 2017-10-18bibliografisk kontrollert
Delarbeid
1. Multivariate characterisation of nitroaromatic compounds
Åpne denne publikasjonen i ny fane eller vindu >>Multivariate characterisation of nitroaromatic compounds
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
urn:nbn:se:oru:diva-15586 (URN)
Tilgjengelig fra: 2011-05-16 Laget: 2011-05-16 Sist oppdatert: 2017-10-17bibliografisk kontrollert
2. Analysis of nitroaromatic compounds in complex samples using solid-phase microextraction and isotope dilution quantification gas chromatography-electron-capture negative ionisation mass spectrometry
Åpne denne publikasjonen i ny fane eller vindu >>Analysis of nitroaromatic compounds in complex samples using solid-phase microextraction and isotope dilution quantification gas chromatography-electron-capture negative ionisation mass spectrometry
2007 (engelsk)Inngår i: Journal of Chromatography A, ISSN 0021-9673, E-ISSN 1873-3778, Vol. 1164, nr 1-2, s. 65-73Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A solid-phase microextraction (SPME) method using gas chromatography–electron-capture negative ionisation mass spectrometry (GC–ECNI-MS) and isotope dilution quantification for the analysis of nitroaromatic compounds in complex, water based samples has been optimised. For ionisation, ECNI was the most sensitive and selective method. SPME was compared to solid-phase extraction (SPE) and found to be more sensitive for these small volume samples. LODs were in the range 0.02–38 ng L−1 for SPME and 6–184 ng L−1 for SPE, respectively. The SPME method was applied on samples in the ng L−1 level from artificial reed beds treated with sludge containing residues from explosives and pharmaceuticals.

sted, utgiver, år, opplag, sider
Amsterdam: Elsevier, 2007
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
urn:nbn:se:oru:diva-2905 (URN)10.1016/j.chroma.2007.07.023 (DOI)
Tilgjengelig fra: 2008-02-15 Laget: 2008-02-15 Sist oppdatert: 2017-12-14bibliografisk kontrollert
3. Determination of 2,4,6-trichloroanisole and 2,4,6-tribromoanisole on ng L-1 to pg L-1 levels in wine by soild-phase microextraction and gas chromatography-high-resolution mass spectrometry
Åpne denne publikasjonen i ny fane eller vindu >>Determination of 2,4,6-trichloroanisole and 2,4,6-tribromoanisole on ng L-1 to pg L-1 levels in wine by soild-phase microextraction and gas chromatography-high-resolution mass spectrometry
Vise andre…
2006 (engelsk)Inngår i: Journal of Chromatography A, ISSN 0021-9673, E-ISSN 1873-3778, Vol. 1111, nr 1, s. 71-75Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A gas chromatography-high-resolution mass spectrometry (GC-HRMS) method using solid-phase microextraction (SPME) for the determination of 2,4,6-trichloroanisole (TCA) and 2,4,6-tribromoanisole (TBA) in wine at low ng L−1 levels was developed. A robust SPME method was developed by optimizing several different parameters, including type of fiber, salt addition, sample volume, extraction and desorption time. The quantification limit for TCA and TBA in wine was lowered substantially using GC-HRMS in combination with the optimized SPME method and allowed the detection of low analyte concentrations (ng L−1) with good accuracy. Limits of quantification for red wine of 0.3 ng L−1 for TCA and 0.2 ng L−1 for TBA with gas chromatography-negative chemical ionization mass spectrometry and 0.03 ng L−1 for TCA and TBA were achieved using GC-HRMS. The method was applied to 30 wines of which 4 wines were sensorically qualified as cork defected. TCA was found in three of these wines with concentrations in the range 2–25 ng L−1. TBA was not detected in any of the samples.

HSV kategori
Forskningsprogram
Kemi
Identifikatorer
urn:nbn:se:oru:diva-2906 (URN)10.1016/j.chroma.2006.01.096 (DOI)
Tilgjengelig fra: 2008-02-15 Laget: 2008-02-15 Sist oppdatert: 2017-12-14bibliografisk kontrollert
4. Determination of 2,4,6-trichloroanisole and 2,4,6-tribromoanisole in wine using microextraction in packed syringe and gas chromatography mass spectrometry
Åpne denne publikasjonen i ny fane eller vindu >>Determination of 2,4,6-trichloroanisole and 2,4,6-tribromoanisole in wine using microextraction in packed syringe and gas chromatography mass spectrometry
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
urn:nbn:se:oru:diva-2907 (URN)
Tilgjengelig fra: 2008-02-15 Laget: 2008-02-15 Sist oppdatert: 2017-10-18bibliografisk kontrollert

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