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A ionic liquid for dispersive liquid-liquid microextraction of phenols
Abstract
In the present study, a new solvent-free mode of liquid phase microextraction termed ionic liquid dispersive liquid-liquid microextraction ( IL-DLLME ) was developed. Four phenols were used as model compounds in the development and evaluation of the procedure. In this method, 50 µL of ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([Bmim][PF 6 ]) and 1.5 mL of sample aqueous solution were placed in a 2.2-mL glass test tube and mixed by aspirating and rapidly injecting by a syringe. This procedure produced a cloudy solution. In this process, phenols in the water sample were extracted into the IL phase. After centrifuging, the fine droplets of IL sedimented to the bottom of the glass test tube. The settled phase was injected into the high performance liquid chromatograph (HPLC) for separation and detection of phenols. Some parameters that might affect the extraction efficiency were optimized. The main advantages of the proposed method are high speed, high recovery, good repeatability and environmental friendliness.
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Dispersion in DLLME can be achieved by ultrasound or by repeatedly aspiring and injecting the sample with the disperser solvent.
“In other cases, dispersion is by ultrasound [17] or repeatedly aspiring and injecting the sample with the disperser solvent [18,19].”
From Dispersive liquid-liquid microextraction for determination of organic analytes (2010) · cites this paper as [18]
IL-DLLME has a drawback of a wide peak at the beginning of the chromatogram corresponding to the IL.
“As can be seen, at the beginning of the chromatogram, there appeared a wide peak, corresponding to the IL - one of the main drawbacks of using IL-DLLME, as already reported [14-19,32,38,47,50,65-67] -although, in this case, it did not interfere at all in the separation.”
From Dispersive liquid-liquid microextraction for determination of organic analytes (2010) · cites this paper as [18]
Chlorinated solvents (chlorobenzene, carbon tetrachloride and chloroform) have been used as extractant solvents for endocrine disrupters, except in two works where IL [BMIm][PF6] and 1-decanol were used.
“Chlorinated solvents have been used as extractant solvents (chlorobenzene, carbon tetrachloride and chloroform), except in two works where IL [BMIm][PF6] [18] and 1-decanol [10] were used.”
From Dispersive liquid-liquid microextraction for determination of organic analytes (2010) · cites this paper as [18]
Endocrine disrupters, antioxidants, PAHs and other organic compounds of different natures have been analyzed by DLLME, IL-DLLME and DLLME-SFO.
“Endocrine disrupters [10,18,57,59,80-83], antioxidants [62,84], PAHs [9,11,66,67,85,86] and other organic compounds of different natures [7,8,63, 87-104] have been analyzed by DLLME, IL-DLLME and DLLME-SFO.”
From Dispersive liquid-liquid microextraction for determination of organic analytes (2010) · cites this paper as [18]
Citations
Cites
Determination of organic compounds in water using dispersive liquid–liquid microextraction
Rezaee, M., Assadi, Y., Milani Hosseini, M.-R., Aghaee, E., Ahmadi, F., & Berijani, S. (2006) · Journal of Chromatography A · doi:10.1016/j.chroma.2006.03.007 · Cited by 3,402
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Research works printed but not linked: 21
- Hou, L. and Lee, H.K., Anal. Chem., 2003, vol. 75, no. 11, p. 2784. · DOI
- Psillakis, E. and Kalogerakis, N., Trends Anal. Chem., 2002, vol. 21, no. 1, p. 54. · DOI · Paper page
- Liu, J.F., Jiang, G.B., Chi, Y.G., Cai, Y.Q., Zhou, Q.X. and Hu, J.T., Anal. Chem., 2003, vol. 75, no. 21, p. 5870. · DOI
- Peng, J.F., Liu, J.F., Hu, X.L. and Jiang G.B., J. Chromatogr. A, 2007, vol. 1139, no. 2, p. 165. · DOI · Paper page
- Fattahi, N., Assadi, Y., Hosseini, M.R.M. and Jahromi, E. Z., J. Chromatogr. A, 2007, vol. 1157, nos. 1–2, p. 23. · DOI · Paper page
- Nagaraju, D. and Huang, S.D., J. Chromatogr. A, 2007, vol. 1161, nos. 1–2, p. 89. · DOI · Paper page
- Pino, V., Anderson, J.L., Ayala, J.H., González, V. and Afonso, A.M., J. Chromatogr. A, 2008, vol. 1182, no. 2, p. 145. · DOI
- Zhou, Q.X., Bai, H.H., Xie, G.H. and Xiao, J.P., J. Chromatogr. A, 2008, vol. 1177, no. 1, p. 43. · DOI · Paper page
- Sharova, E.V., Artyushin, O.I., Shaplov, A.S., Myasoedova, G.V. and Odinets, I.L., Tetrahedron Lett., 2008, vol. 49, no. 10, p. 1641. · DOI
- Gong, K., Wang, H.L., Fang, D. and Liu, Z.L., Catal. Commun., 2008, vol. 9, no. 5, p. 650. · DOI
- Deng, M.J., Chen, P.Y., Leong, T.I., Sun, I.W., Chang, J.K. and Tsai, W.T., Electrochem. Commun., 2008, vol. 10, no. 2, p. 213. · DOI
- Xiang, C.L., Zou, Y.J., Sun, L.X. and Xu, F., Electrochem. Commun., 2008, vol. 10, no. 1, p. 38. · DOI
- Wang, J.J., Pei, Y.C., Zhao, Y. and Hu, Z.G., Green Chem., 2005, vol. 7, no. 4, p. 196. · DOI
- Huddleston, J.G., Visser, A.E., Reichert, W.M., Willauer, H.D., Broker, G.A. and Rogers, R.D., Green Chem., 2001, vol. 3, no. 4, p. 156. · DOI
- Shimojo, K. and Goto, M., Anal. Chem., 2004, vol. 76, no. 17, p. 5039. · DOI
- Zhao, L.M., Zhu, L.Y. and Lee, H.K., J. Chromatogr. A, 2002, vol. 963, nos. 1–2, p. 239. · DOI
- Peng, J.F., Liu, J.F., Jiang, G.B., Tai, C. and Huang, M.J., J. Chromatogr. A, 2005, vol. 1072, no. 1, p. 3. · DOI
- Dean, J.A., Lange’s Handbook of Chemistry, 14th edn. McGraw-Hill, New York, 1992.
- Peng, X.Z., Wang, Z.D., Yang, C., Chen, F.R. and Mai, B.X., J. Chromatogr. A, 2006, vol. 1116, nos. 1–2, p. 51. · DOI
- Ye, C.L., Zhou, Q.X., Wang, X.M. and Xiao, J.P., J. Sep. Sci., 2007, vol. 30, no. 1, p. 42. · DOI
- Simões, N.G., Cardoso, V.V., Ferreira, E., Benoliel, M.J. and Almeida, C.M.M., Chemosphere, 2007, vol. 68, no. 3, p. 501. · DOI
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Ionic liquids in dispersive liquid-liquid microextraction
Trujillo-Rodríguez, M. J., Rocío-Bautista, P., Pino, V., & Afonso, A. M. (2013) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2013.06.008 · Cited by 276
Dispersive liquid-liquid microextraction for determination of organic analytes
Herrera-Herrera, A. V., Asensio-Ramos, M., Hernández-Borges, J., & Rodríguez-Delgado, M. Á. (2010) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2010.03.016 · Cited by 267
The roles of ionic liquids in sorptive microextraction techniques
Aguilera-Herrador, E., Lucena, R., Cárdenas, S., & Valcárcel, M. (2010) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2009.11.009 · Cited by 171
Ten years of dispersive liquid–liquid microextraction and derived techniques
Campillo, N., Viñas, P., Šandrejová, J., & Andruch, V. (2017) · Applied Spectroscopy Reviews · doi:10.1080/05704928.2016.1224240 · Cited by 102
Metadata
- Authors
- Fan, Y. C., Chen, M. L., Shen-Tu, C., & Zhu, Y.
- Affiliations
- Henan Polytechnic University (CN)
- Zhejiang Shuren University (CN)
- Zhejiang University (CN)
- ORCID
- Venue
- Journal of Analytical Chemistry
- Publisher
- Pleiades Publishing Ltd
- Published
- 2009-10
- Volume
- 64
- Issue
- 10
- Pages
- 1017-1022
- ISSN
- 0021-8766 (ISSN-L)
- 1061-9348
- 1608-3199
- OpenAlex
- W2087804647
- Cited by
- 43
- References
- 1
- Citations by year
- 2024: 1 · 2022: 1 · 2020: 1 · 2019: 2 · 2018: 2 · 2016: 2 · 2015: 3 · 2014: 3 · 2013: 4 · 2012: 10
- FWCI
- 7.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Analytical Chemistry (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Analytical Chemistry › Analytical chemistry methods development
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Ionic liquids properties and applications
- Physical Sciences › Chemistry › Analytical Chemistry › Analytical Chemistry and Chromatography
- Keywords
- ionic liquid dispersive liquid-liquid microextraction, phenols, 1-butyl-3-methylimidazolium hexafluorophosphate, solvent-free extraction, water sample analysis, extraction efficiency optimization, HPLC determination
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