Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid–liquid microextraction and electrothermal atomic absorption spectrometry. Issue 2 (25th November 2014)
- Record Type:
- Journal Article
- Title:
- Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid–liquid microextraction and electrothermal atomic absorption spectrometry. Issue 2 (25th November 2014)
- Main Title:
- Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid–liquid microextraction and electrothermal atomic absorption spectrometry
- Authors:
- Grijalba, Alexander Castro
Escudero, Leticia B.
Wuilloud, Rodolfo G. - Abstract:
- Abstract : Different phosphonium ionic liquids have been assayed for liquid–liquid microextraction of As species. Abstract : The capabilities of several phosphonium-ionic liquids (PILs) to form ion-pairs with a complex obtained by reaction of arsenate species with molybdate were evaluated. Phosphonium-ILs containing the tetradecyl(trihexyl)phosphonium cation but different anions (dicyanamide and decanoate) and tributyl(methyl)phosphonium methylsulphate IL were studied. The size, polarity and localization of charges in PIL cations were shown to influence their capability to form ion-pairs with the arsenomolybdate (AsMo12 O40 3− ) complex and to extract As(v ). The performance of PILs was compared with that of a widely used ion-pairing reagent, cetyltrimethylammonium bromide (CTAB). Finally, the IL tetradecyl(trihexyl)phosphonium dicyanamide was chosen to develop a liquid–liquid microextraction (LLME) procedure using only 80 μL of tetrachloroethylene as the extractant. The organic phase was directly injected into the graphite furnace of an electrothermal atomic absorption spectrometer (ETAAS) for As determination. An extraction efficiency of 100% and a sensitivity enhancement factor of 130 were obtained with 5 mL of sample. The detection limit was 1.9 ng L −1 and the relative standard deviation for six replicate measurements of 1.0 μg L −1 for As was 4.9%, 5.0% and 5.1% for As(v ), As(iii ) and organic As species, respectively.
- Is Part Of:
- Analytical methods. Volume 7:Issue 2(2015)
- Journal:
- Analytical methods
- Issue:
- Volume 7:Issue 2(2015)
- Issue Display:
- Volume 7, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2015-0007-0002-0000
- Page Start:
- 490
- Page End:
- 499
- Publication Date:
- 2014-11-25
- Subjects:
- Chemistry, Analytic -- Periodicals
Analytical biochemistry -- Periodicals
Chemical laboratories -- Standards -- Periodicals
543.1905 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/AY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c4ay02324b ↗
- Languages:
- English
- ISSNs:
- 1759-9660
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0897.103700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10125.xml