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采用毛细管电泳-质谱联用技术分析采出水样中的环烷酸。

Analysis of naphthenic acids in produced water samples by capillary electrophoresis-mass spectrometry.

作者信息

Pinheiro Kemilly M P, Sako Alysson V F, Rodrigues Marcella F, Vaz Boniek G, Medeiros Junior Iris, Carvalho Rogerio M, Coltro Wendell K T

机构信息

Instituto de Química, Universidade Federal de Goiás, Goiânia, Brazil.

Instituto de Química, Universidade Federal da Santa Catarina, Florianópolis, Brazil.

出版信息

J Sep Sci. 2023 Oct;46(19):e2300442. doi: 10.1002/jssc.202300442. Epub 2023 Aug 15.

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.

摘要

采用毛细管电泳-质谱法分析采出水中的环烷酸。使用由40 mmol/L氢氧化铵、32 mmol/L乙酸和20%(v/v)异丙醇组成的pH 8.6缓冲液,在约13分钟内可检测到环戊烷羧酸、苯甲酸、环己烷丁酸、1-萘甲酸、癸酸、3,5-二甲基金刚烷-1-羧酸、9-蒽羧酸和十五烷酸。所提出的方法具有良好的重复性,峰面积总和的相对标准偏差(RSD)值为6.6%,分析时间的RSD值小于2%。在日间分析中,峰面积总和和迁移时间的RSD值分别为10.3%和10%。所开发的方法在苯甲酸、癸酸、3,5-二甲基金刚烷-1-羧酸和9-蒽羧酸浓度范围为5至50 mg/L,以及环戊烷羧酸、环己烷丁酸、1-萘甲酸和十五烷酸浓度范围为10至50 mg/L时呈现线性行为。检测限范围为0.31至1.64 mg/L。对六个采出水样品进行了分析,能够鉴定和定量环戊烷羧酸、苯甲酸、环己烷丁酸和癸酸。浓度在4.8至98.9 mg/L之间变化,证明该方法在复杂样品的应用中有效。

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