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M.T. Galceran

Researcher at University of Barcelona

Publications -  132
Citations -  5572

M.T. Galceran is an academic researcher from University of Barcelona. The author has contributed to research in topics: Mass spectrometry & Solid phase extraction. The author has an hindex of 45, co-authored 132 publications receiving 5299 citations.

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The application of gas chromatography to environmental analysis

TL;DR: The use of gas chromatography in the analysis of persistent organic contaminants in air, water, soils, sediments and biota is discussed in this paper, with a focus on sample-preparation techniques.
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Analysis of bisphenols in soft drinks by on-line solid phase extraction fast liquid chromatography–tandem mass spectrometry

TL;DR: An automated on-line solid-phase extraction coupled to fast liquid chromatography-tandem mass spectrometry (on-line SPE fast LC-MS/MS) method was developed for the simultaneous analysis of bisphenol A (BPA), bispenol F (BPF), bistonhenol E (BPE), bishenol B (BPB) and bisphensol S (BPS) in canned soft drinks without any previous sample treatment.
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Modern developments in gas chromatography-mass spectrometry-based environmental analysis.

TL;DR: An overview of recent developments and applications of the GC-MS technique in relation to the analysis in environmental samples of known persistent pollutants and some emerging contaminants is presented in this paper, where the use of different mass analysers such as linear quadrupole, quadrapole ion-trap, double-focusing sectors and time-of-flight analysers is examined.
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Determination, synthesis and survey of iodinated trihalomethanes in water treatment processes

TL;DR: In this article, six ITHMs (CHCl2I, CHClI2, CHBr2I and CHBrClI) have been synthesized in order to evaluate headspace (HS), purge and trap (PT), whereas P&T and CLSA with gas chromatography and mass spectrometry (GC/MS).
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Determination of chlorophenols by solid-phase microextraction and liquid chromatography with electrochemical detection

TL;DR: The precision of the SPME-LC-ED method was linear over three to four orders of magnitude and the detection limits were lower than the European Community legislation limits for drinking water and wood samples.