Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate
A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which inc...
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description | A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. Intra‐ and interday precisions of the present method were satisfactory with relative standard deviations of 1.7 and 2.1%, respectively. |
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In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. Intra‐ and interday precisions of the present method were satisfactory with relative standard deviations of 1.7 and 2.1%, respectively.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.201700205</identifier><identifier>PMID: 28748649</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>crown ethers ; Extraction processes ; Hydrophobicity ; ion chromatography ; Linearity ; Liquid-liquid extraction ; Nitric acid ; Octanol ; Strontium ; vortex‐assisted liquid–liquid microextraction ; Vortices</subject><ispartof>Journal of separation science, 2017-10, Vol.40 (19), p.3866-3872</ispartof><rights>2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4055-e085581b2f2331650c23aca697d40cd42b7eb0c77e04b8cda34bf3c081c17c623</citedby><cites>FETCH-LOGICAL-c4055-e085581b2f2331650c23aca697d40cd42b7eb0c77e04b8cda34bf3c081c17c623</cites><orcidid>0000-0001-5243-2700</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjssc.201700205$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjssc.201700205$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28748649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Chin‐Yi</creatorcontrib><creatorcontrib>Chang, Da‐An</creatorcontrib><creatorcontrib>Shen, Yuzhou</creatorcontrib><creatorcontrib>Sun, Yuh‐Chang</creatorcontrib><creatorcontrib>Wu, Chien‐Hou</creatorcontrib><title>Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate</title><title>Journal of separation science</title><addtitle>J Sep Sci</addtitle><description>A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. Intra‐ and interday precisions of the present method were satisfactory with relative standard deviations of 1.7 and 2.1%, respectively.</description><subject>crown ethers</subject><subject>Extraction processes</subject><subject>Hydrophobicity</subject><subject>ion chromatography</subject><subject>Linearity</subject><subject>Liquid-liquid extraction</subject><subject>Nitric acid</subject><subject>Octanol</subject><subject>Strontium</subject><subject>vortex‐assisted liquid–liquid microextraction</subject><subject>Vortices</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkc2O0zAUhS0EYn5gyxJZYtORaLEdO7GXqOJXI7EYYBs5jsO4cuKO7ajNro-AxIMgwRv1SbhVhy7YsDnnWvp8j62D0DNKFpQQ9mqVklkwQis4EPEAndOSirkqKH94mkl5hi5SWhHApCKP0RmTFZclV-fo59cQs93ud991Si5l22Lv7kbX7nc_jgPunYnBbnPUJrsw4NDhlGMYsht73MXQ443ONuKk-7W3CY_JDd8w3-9-vQT5PRMgVxDQOpAZkBm8GfPkzWR8uLVbPYQDQCUIZG0G8BLrocXZQuz61g6Tb0KEmCfoUad9sk_v_RJ9efvm8_L9_PrTuw_L19dzw4kQc0ukEJI2rGNFQUtBDCu00aWqWk5My1lT2YaYqrKEN9K0uuBNVxgiqaGVKVlxiWbHvesY7kabct27ZKz3erBhTDVVjAupVCkAffEPugpjHOB1QHFZMCWZAmpxpOCDKUXb1evoeh2nmpL6UGV9qLI-VQkXnt-vHZvetif8b3cA8COwcd5O_1lXf7y5WQqhRPEHMl24Bw</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Wang, Chin‐Yi</creator><creator>Chang, Da‐An</creator><creator>Shen, Yuzhou</creator><creator>Sun, Yuh‐Chang</creator><creator>Wu, Chien‐Hou</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5243-2700</orcidid></search><sort><creationdate>201710</creationdate><title>Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate</title><author>Wang, Chin‐Yi ; Chang, Da‐An ; Shen, Yuzhou ; Sun, Yuh‐Chang ; Wu, Chien‐Hou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4055-e085581b2f2331650c23aca697d40cd42b7eb0c77e04b8cda34bf3c081c17c623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>crown ethers</topic><topic>Extraction processes</topic><topic>Hydrophobicity</topic><topic>ion chromatography</topic><topic>Linearity</topic><topic>Liquid-liquid extraction</topic><topic>Nitric acid</topic><topic>Octanol</topic><topic>Strontium</topic><topic>vortex‐assisted liquid–liquid microextraction</topic><topic>Vortices</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Chin‐Yi</creatorcontrib><creatorcontrib>Chang, Da‐An</creatorcontrib><creatorcontrib>Shen, Yuzhou</creatorcontrib><creatorcontrib>Sun, Yuh‐Chang</creatorcontrib><creatorcontrib>Wu, Chien‐Hou</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Chin‐Yi</au><au>Chang, Da‐An</au><au>Shen, Yuzhou</au><au>Sun, Yuh‐Chang</au><au>Wu, Chien‐Hou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2017-10</date><risdate>2017</risdate><volume>40</volume><issue>19</issue><spage>3866</spage><epage>3872</epage><pages>3866-3872</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. Intra‐ and interday precisions of the present method were satisfactory with relative standard deviations of 1.7 and 2.1%, respectively.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28748649</pmid><doi>10.1002/jssc.201700205</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-5243-2700</orcidid></addata></record> |
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subjects | crown ethers Extraction processes Hydrophobicity ion chromatography Linearity Liquid-liquid extraction Nitric acid Octanol Strontium vortex‐assisted liquid–liquid microextraction Vortices |
title | Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate |
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