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      Recent Advances in Applications of Ionic Liquids in Miniaturized Microextraction Techniques

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          Abstract

          Green sample preparation is one of the most challenging aspects in green analytical chemistry. In this framework, miniaturized microextraction techniques have been developed and are widely performed due to their numerous positive features such as simplicity, limited need for organic solvents, instrumentation of low cost and short time of extraction. Also, ionic liquids (ILs) have unequivocally a “green” character, which they owe to their unique properties including the re-usage, the high reaction efficiency and selectivity in room temperature, the ability to dissolve both organic and inorganic compounds, and thermal stability. In the present review, the recent advances in the application of ionic liquids in miniaturized liquid and solid phase extraction techniques as extractants, intermediate solvents, mediators and desorption solvents are discussed, quoting the advantages and drawbacks of each individual technique. Some of the most important sample preparation techniques covered include solid-phase microextraction (SPME), dispersive liquid-liquid microextraction (DLLME), single-drop microextraction (SDME), stir bar sorptive extraction (SBSE), and stir cake sorptive extraction (SCSE).

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          Applications of ionic liquids in the chemical industry.

          In contrast to a recently expressed, and widely cited, view that "Ionic liquids are starting to leave academic labs and find their way into a wide variety of industrial applications", we demonstrate in this critical review that there have been parallel and collaborative exchanges between academic research and industrial developments since the materials were first reported in 1914 (148 references).
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            Determination of organic compounds in water using dispersive liquid-liquid microextraction.

            A new microextraction technique termed dispersive liquid-liquid microextraction (DLLME) was developed. DLLME is a very simple and rapid method for extraction and preconcentration of organic compounds from water samples. In this method, the appropriate mixture of extraction solvent (8.0 microL C2Cl4) and disperser solvent (1.00 mL acetone) are injected into the aqueous sample (5.00 mL) by syringe, rapidly. Therefore, cloudy solution is formed. In fact, it is consisted of fine particles of extraction solvent which is dispersed entirely into aqueous phase. After centrifuging, the fine particles of extraction solvent are sedimented in the bottom of the conical test tube (5.0 +/- 0.2 microL). The performance of DLLME is illustrated with the determination of polycyclic aromatic hydrocarbons (PAHs) in water samples by using gas chromatography-flame ionization detection (GC-FID). Some important parameters, such as kind of extraction and disperser solvent and volume of them, and extraction time were investigated. Under the optimum conditions the enrichment factor ranged from 603 to 1113 and the recovery ranged from 60.3 to 111.3%. The linear range was 0.02-200 microg/L (four orders of magnitude) and limit of detection was 0.007-0.030 microg/L for most of analytes. The relative standard deviations (RSDs) for 2 microg/L of PAHs in water by using internal standard were in the range 1.4-10.2% (n = 5). The recoveries of PAHs from surface water at spiking level of 5.0 microg/L were 82.0-111.0%. The ability of DLLME technique in the extraction of other organic compounds such as organochlorine pesticides, organophosphorus pesticides and substituted benzene compounds (benzene, toluene, ethyl benzene, and xylenes) from water samples were studied. The advantages of DLLME method are simplicity of operation, rapidity, low cost, high recovery, and enrichment factor.
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              Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
                MDPI
                1420-3049
                13 June 2018
                June 2018
                : 23
                : 6
                : 1437
                Affiliations
                Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece; marikiss@ 123456chem.auth.gr
                Author notes
                [* ]Correspondence: samanidu@ 123456chem.auth.gr ; Tel.: +30-231-099-7698
                Author information
                https://orcid.org/0000-0002-8493-1106
                Article
                molecules-23-01437
                10.3390/molecules23061437
                6099658
                29899277
                7316eedd-f07c-49a8-97db-696e1bc1d125
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 14 May 2018
                : 12 June 2018
                Categories
                Review

                ionic liquids,sample preparation,microextraction,solid-phase microextraction,dispersive liquid-liquid microextraction,single-drop microextraction,stir bar sorptive extraction,stir cake sorptive extraction

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