Analysis of naphthenic acids in produced water samples by capillary electrophoresis‐mass spectrometry
A capillary electrophoresis‐mass spectrometry method was used to analyze naphthenic acids in produced water samples. It was possible to detect cyclopentanecarboxylic, benzoic, cyclohexanebutyric, 1‐naphthoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic, 9‐anthracenecarboxylic, and pentadecanoic ac...
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Veröffentlicht in: | Journal of separation science 2023-10, Vol.46 (19), p.e2300442-e2300442 |
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container_title | Journal of separation science |
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creator | Pinheiro, Kemilly M. P. Sako, Alysson V. F. Rodrigues, Marcella F. Vaz, Boniek G. Medeiros Junior, Iris Carvalho, Rogerio M. Coltro, Wendell K. T. |
description | A capillary electrophoresis‐mass spectrometry method was used to analyze naphthenic acids in produced water samples. It was possible to detect cyclopentanecarboxylic, benzoic, cyclohexanebutyric, 1‐naphthoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic, 9‐anthracenecarboxylic, and pentadecanoic acids within ca. 13 min using a buffer composed of 40 mmol/L ammonium hydroxide, 32 mmol/L acetic acid and 20% v/v isopropyl alcohol, pH 8.6. The proposed method showed good repeatability, with relative standard deviation (RSD) values of 6.6% for the sum of the peak areas and less than 2% for the analysis time. In the interday analysis, the RSD values for the sum of the peak areas and migration time were 10.3% and 10%, respectively. The developed method demonstrated linear behavior in the concentration range between 5 and 50 mg/L for benzoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic and 9‐anthracenecarboxylic acids, and between 10 and 50 mg/L for cyclopentanecarboxylic, cyclohexanebutyric, 1‐ naphthoic, and pentadecanoic acids. The detection limits values ranged from 0.31 to 1.64 mg/L. Six produced water samples were analyzed and it was possible to identify and quantify cyclopentanecarboxylic, benzoic, cyclohexanebutyric, and decanoic acids. The concentrations varied between 4.8 and 98.9 mg/L, proving effective in the application of complex samples. |
doi_str_mv | 10.1002/jssc.202300442 |
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P. ; Sako, Alysson V. F. ; Rodrigues, Marcella F. ; Vaz, Boniek G. ; Medeiros Junior, Iris ; Carvalho, Rogerio M. ; Coltro, Wendell K. T.</creator><creatorcontrib>Pinheiro, Kemilly M. P. ; Sako, Alysson V. F. ; Rodrigues, Marcella F. ; Vaz, Boniek G. ; Medeiros Junior, Iris ; Carvalho, Rogerio M. ; Coltro, Wendell K. T.</creatorcontrib><description>A capillary electrophoresis‐mass spectrometry method was used to analyze naphthenic acids in produced water samples. It was possible to detect cyclopentanecarboxylic, benzoic, cyclohexanebutyric, 1‐naphthoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic, 9‐anthracenecarboxylic, and pentadecanoic acids within ca. 13 min using a buffer composed of 40 mmol/L ammonium hydroxide, 32 mmol/L acetic acid and 20% v/v isopropyl alcohol, pH 8.6. The proposed method showed good repeatability, with relative standard deviation (RSD) values of 6.6% for the sum of the peak areas and less than 2% for the analysis time. In the interday analysis, the RSD values for the sum of the peak areas and migration time were 10.3% and 10%, respectively. The developed method demonstrated linear behavior in the concentration range between 5 and 50 mg/L for benzoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic and 9‐anthracenecarboxylic acids, and between 10 and 50 mg/L for cyclopentanecarboxylic, cyclohexanebutyric, 1‐ naphthoic, and pentadecanoic acids. The detection limits values ranged from 0.31 to 1.64 mg/L. Six produced water samples were analyzed and it was possible to identify and quantify cyclopentanecarboxylic, benzoic, cyclohexanebutyric, and decanoic acids. The concentrations varied between 4.8 and 98.9 mg/L, proving effective in the application of complex samples.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.202300442</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Acetic acid ; Acids ; Ammonium hydroxide ; Analytical chemistry ; Capillary electrophoresis ; Chemical compounds ; Electrophoresis ; Isopropanol ; Mass spectrometry ; Naphthenic acids ; Predictions ; Scientific imaging ; Water sampling</subject><ispartof>Journal of separation science, 2023-10, Vol.46 (19), p.e2300442-e2300442</ispartof><rights>2023 Wiley‐VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c255t-497c09196de8241c3c0caa85ec765ccc0757293e76fca3b554f1eb43434a02103</cites><orcidid>0000-0002-4009-2291</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Pinheiro, Kemilly M. P.</creatorcontrib><creatorcontrib>Sako, Alysson V. F.</creatorcontrib><creatorcontrib>Rodrigues, Marcella F.</creatorcontrib><creatorcontrib>Vaz, Boniek G.</creatorcontrib><creatorcontrib>Medeiros Junior, Iris</creatorcontrib><creatorcontrib>Carvalho, Rogerio M.</creatorcontrib><creatorcontrib>Coltro, Wendell K. T.</creatorcontrib><title>Analysis of naphthenic acids in produced water samples by capillary electrophoresis‐mass spectrometry</title><title>Journal of separation science</title><description>A capillary electrophoresis‐mass spectrometry method was used to analyze naphthenic acids in produced water samples. It was possible to detect cyclopentanecarboxylic, benzoic, cyclohexanebutyric, 1‐naphthoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic, 9‐anthracenecarboxylic, and pentadecanoic acids within ca. 13 min using a buffer composed of 40 mmol/L ammonium hydroxide, 32 mmol/L acetic acid and 20% v/v isopropyl alcohol, pH 8.6. The proposed method showed good repeatability, with relative standard deviation (RSD) values of 6.6% for the sum of the peak areas and less than 2% for the analysis time. In the interday analysis, the RSD values for the sum of the peak areas and migration time were 10.3% and 10%, respectively. The developed method demonstrated linear behavior in the concentration range between 5 and 50 mg/L for benzoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic and 9‐anthracenecarboxylic acids, and between 10 and 50 mg/L for cyclopentanecarboxylic, cyclohexanebutyric, 1‐ naphthoic, and pentadecanoic acids. The detection limits values ranged from 0.31 to 1.64 mg/L. Six produced water samples were analyzed and it was possible to identify and quantify cyclopentanecarboxylic, benzoic, cyclohexanebutyric, and decanoic acids. The concentrations varied between 4.8 and 98.9 mg/L, proving effective in the application of complex samples.</description><subject>Acetic acid</subject><subject>Acids</subject><subject>Ammonium hydroxide</subject><subject>Analytical chemistry</subject><subject>Capillary electrophoresis</subject><subject>Chemical compounds</subject><subject>Electrophoresis</subject><subject>Isopropanol</subject><subject>Mass spectrometry</subject><subject>Naphthenic acids</subject><subject>Predictions</subject><subject>Scientific imaging</subject><subject>Water sampling</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkE1Lw0AQhhdRsFavnhe8eEmd3c3m41iKX1DwouewnU5sSr7cSZDc_An-Rn-JiUoPMocZhoeXmUeISwULBaBv9sy40KANQBjqIzFTkbJBalR4fJghOhVnzHsAFScpzMTrsnblwAXLJpe1a3fdjuoCpcNiy7KoZeubbY-0le-uIy_ZVW1JLDeDRNcWZen8IKkk7HzT7hpPY9TXx2flmCW3P-uKOj-ci5PclUwXf30uXu5un1cPwfrp_nG1XAeore2CMI0RUpVGW0p0qNAgoHOJJYwji4gQ21inhuIoR2c21oa5ok1oxnKgFZi5uP7NHe9-64m7rCoYabyzpqbnTCdWJVESpRN69Q_dN70fdUxUbCKjwaqRWvxS6BtmT3nW-qIav84UZJP3bPKeHbybb6F9eG8</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Pinheiro, Kemilly M. P.</creator><creator>Sako, Alysson V. F.</creator><creator>Rodrigues, Marcella F.</creator><creator>Vaz, Boniek G.</creator><creator>Medeiros Junior, Iris</creator><creator>Carvalho, Rogerio M.</creator><creator>Coltro, Wendell K. T.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4009-2291</orcidid></search><sort><creationdate>20231001</creationdate><title>Analysis of naphthenic acids in produced water samples by capillary electrophoresis‐mass spectrometry</title><author>Pinheiro, Kemilly M. P. ; Sako, Alysson V. F. ; Rodrigues, Marcella F. ; Vaz, Boniek G. ; Medeiros Junior, Iris ; Carvalho, Rogerio M. ; Coltro, Wendell K. T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c255t-497c09196de8241c3c0caa85ec765ccc0757293e76fca3b554f1eb43434a02103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetic acid</topic><topic>Acids</topic><topic>Ammonium hydroxide</topic><topic>Analytical chemistry</topic><topic>Capillary electrophoresis</topic><topic>Chemical compounds</topic><topic>Electrophoresis</topic><topic>Isopropanol</topic><topic>Mass spectrometry</topic><topic>Naphthenic acids</topic><topic>Predictions</topic><topic>Scientific imaging</topic><topic>Water sampling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pinheiro, Kemilly M. P.</creatorcontrib><creatorcontrib>Sako, Alysson V. F.</creatorcontrib><creatorcontrib>Rodrigues, Marcella F.</creatorcontrib><creatorcontrib>Vaz, Boniek G.</creatorcontrib><creatorcontrib>Medeiros Junior, Iris</creatorcontrib><creatorcontrib>Carvalho, Rogerio M.</creatorcontrib><creatorcontrib>Coltro, Wendell K. T.</creatorcontrib><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>Pinheiro, Kemilly M. P.</au><au>Sako, Alysson V. F.</au><au>Rodrigues, Marcella F.</au><au>Vaz, Boniek G.</au><au>Medeiros Junior, Iris</au><au>Carvalho, Rogerio M.</au><au>Coltro, Wendell K. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of naphthenic acids in produced water samples by capillary electrophoresis‐mass spectrometry</atitle><jtitle>Journal of separation science</jtitle><date>2023-10-01</date><risdate>2023</risdate><volume>46</volume><issue>19</issue><spage>e2300442</spage><epage>e2300442</epage><pages>e2300442-e2300442</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>A capillary electrophoresis‐mass spectrometry method was used to analyze naphthenic acids in produced water samples. It was possible to detect cyclopentanecarboxylic, benzoic, cyclohexanebutyric, 1‐naphthoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic, 9‐anthracenecarboxylic, and pentadecanoic acids within ca. 13 min using a buffer composed of 40 mmol/L ammonium hydroxide, 32 mmol/L acetic acid and 20% v/v isopropyl alcohol, pH 8.6. The proposed method showed good repeatability, with relative standard deviation (RSD) values of 6.6% for the sum of the peak areas and less than 2% for the analysis time. In the interday analysis, the RSD values for the sum of the peak areas and migration time were 10.3% and 10%, respectively. The developed method demonstrated linear behavior in the concentration range between 5 and 50 mg/L for benzoic, decanoic, 3,5‐dimethyladamantane‐1‐carboxylic and 9‐anthracenecarboxylic acids, and between 10 and 50 mg/L for cyclopentanecarboxylic, cyclohexanebutyric, 1‐ naphthoic, and pentadecanoic acids. The detection limits values ranged from 0.31 to 1.64 mg/L. Six produced water samples were analyzed and it was possible to identify and quantify cyclopentanecarboxylic, benzoic, cyclohexanebutyric, and decanoic acids. The concentrations varied between 4.8 and 98.9 mg/L, proving effective in the application of complex samples.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jssc.202300442</doi><orcidid>https://orcid.org/0000-0002-4009-2291</orcidid></addata></record> |
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subjects | Acetic acid Acids Ammonium hydroxide Analytical chemistry Capillary electrophoresis Chemical compounds Electrophoresis Isopropanol Mass spectrometry Naphthenic acids Predictions Scientific imaging Water sampling |
title | Analysis of naphthenic acids in produced water samples by capillary electrophoresis‐mass spectrometry |
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