Nanosized polymeric fibres for solid-phase microextraction sorbents
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F46747885%3A24620%2F16%3A00000968" target="_blank" >RIV/46747885:24620/16:00000968 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.nanocon.eu/cz/" target="_blank" >http://www.nanocon.eu/cz/</a>
DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Nanosized polymeric fibres for solid-phase microextraction sorbents
Popis výsledku v původním jazyce
Solid phase microextraction (SPME) has been established as a modern, simple, sensitive, rapid and solvent free technique for sample preparation in organic analytical chemistry. Since SPME was first introduced by Pawliszyn in the early 1990s, several modifications of sorbent geometry were developed. The main goal of using electrospun fibres geometry is to enhance the sorbent sensitivity and capacity. In the present work, electrospun polyetherimide (PEI) nanofibres were prepared from 12.5 % solution (80/20 – DMF/THF) fixed on a steel wire solid phase microextraction (SPME) assembly. Analytical performance of prepared fibres was compared with common commercial available SPME fibres (100 µm polydimethylsiloxane (PDMS), 65 µm polydimethylsiloxane/divinylbenzene (PDMS/DVB) and 85 µm polyacrylate (PA)) in the headspace SPME (HS-SPME) mode of gas chromatograph coupled with mass spectrometer (GC/MS/MS). The chlorophenols were chosen as model water pollutants. To solve instability, tailing peaks, detectability and adsorption problems, chlorophenols were acetylated before GC step of the analysis. Lab-made PEI nanofibres assemblies appeared to have sensitivity comparable to commercial SPME fibres.
Název v anglickém jazyce
Nanosized polymeric fibres for solid-phase microextraction sorbents
Popis výsledku anglicky
Solid phase microextraction (SPME) has been established as a modern, simple, sensitive, rapid and solvent free technique for sample preparation in organic analytical chemistry. Since SPME was first introduced by Pawliszyn in the early 1990s, several modifications of sorbent geometry were developed. The main goal of using electrospun fibres geometry is to enhance the sorbent sensitivity and capacity. In the present work, electrospun polyetherimide (PEI) nanofibres were prepared from 12.5 % solution (80/20 – DMF/THF) fixed on a steel wire solid phase microextraction (SPME) assembly. Analytical performance of prepared fibres was compared with common commercial available SPME fibres (100 µm polydimethylsiloxane (PDMS), 65 µm polydimethylsiloxane/divinylbenzene (PDMS/DVB) and 85 µm polyacrylate (PA)) in the headspace SPME (HS-SPME) mode of gas chromatograph coupled with mass spectrometer (GC/MS/MS). The chlorophenols were chosen as model water pollutants. To solve instability, tailing peaks, detectability and adsorption problems, chlorophenols were acetylated before GC step of the analysis. Lab-made PEI nanofibres assemblies appeared to have sensitivity comparable to commercial SPME fibres.
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
CB - Analytická chemie, separace
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/LO1201" target="_blank" >LO1201: ROZVOJ ÚSTAVU PRO NANOMATERIÁLY, POKROČILÉ TECHNOLOGIE A INOVACE TECHNICKÉ UNIVERZITY V LIBERCI</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
NANOCON 2016 - Conference Proceedings, 8th International Conference on Nanomaterials - Research and Application
ISBN
978-80-87294-71-0
ISSN
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e-ISSN
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Počet stran výsledku
5
Strana od-do
314-318
Název nakladatele
Tanger, spol. s.r.o. 2016
Místo vydání
Ostrava
Místo konání akce
Brno
Datum konání akce
1. 1. 2016
Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
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