Instituto de Química, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil.
Instituto de Química, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil; Instituto de Química, Universidade Federal Fluminense, Niterói, RJ 24020-141, Brazil.
J Chromatogr A. 2022 Aug 16;1677:463307. doi: 10.1016/j.chroma.2022.463307. Epub 2022 Jul 5.
This study reports for the first time the use of a microchip electrophoresis (ME) device with integrated capacitively coupled contactless conductivity detection (CD) to analyze naphthenic acids in produced water. A mixture containing 9-anthracenecarboxylic, 1-naphthoic, and benzoic acids was separated and detected using a running buffer composed of 10 mmol L carbonate buffer (pH = 10.2). The separation was achieved within ca. 140 s with baseline resolution greater than 2 and efficiency values ranging from 1.9 × 10 to 2.4 × 10 plates m. The developed methodology provided linear correlation with determination coefficients greater than 0.992 for the concentration ranges between 50 and 250 µmol L for benzoic and 9-anthracenecarboxylic acids, and between 50 and 200 µmol L for 1-naphthoic acid. The achieved limit of detection values varied between 4.7 and 7.7 µmol L. The proposed methodology revealed satisfactory repeatability with RSD values for a sequence of eight injections between 5.5 and 7.7% for peak areas and lower than 1% for migration times. In addition, inter-day precision was evaluated for sixteen injections (a sequence of four injections performed during four days), and the RSD values were lower than 11.5 and 4.9% for peak areas and migration time, respectively. Five produced water samples were analyzed, and it was possible to detect and quantify 9-anthracenecarboxylic acid. The concentrations ranged from 1.05 to 2.24 mmol L with recovery values between 90.8 and 96.0%. ME-CD demonstrated satisfactory analytical performance for determining naphthenic acids in produced water for the first time, which is useful for petroleum or oil industry investigation.
本研究首次报告了使用带有集成电容耦合非接触式电导检测(CD)的微芯片电泳(ME)设备来分析采出水中的环烷酸。使用由 10 mmol L 碳酸盐缓冲液(pH = 10.2)组成的运行缓冲液分离和检测包含 9-蒽羧酸、1-萘酸和苯甲酸的混合物。在约 140 s 内实现了分离,基线分辨率大于 2,效率值范围为 1.9×10 至 2.4×10 板 m。开发的方法学提供了线性相关性,对于苯甲酸和 9-蒽羧酸的浓度范围在 50 至 250 µmol L 之间,以及 1-萘酸的浓度范围在 50 至 200 µmol L 之间,相关系数大于 0.992。实现的检测限值在 4.7 至 7.7 µmol L 之间变化。所提出的方法学具有令人满意的重复性,对于 8 次进样序列,峰面积的 RSD 值在 5.5 至 7.7%之间,而迁移时间的 RSD 值低于 1%。此外,在 16 次进样(在四天期间进行的四次进样序列)期间评估了日间精密度,并且 RSD 值分别低于峰面积和迁移时间的 11.5%和 4.9%。分析了五个采出水样品,能够检测和定量 9-蒽羧酸。浓度范围为 1.05 至 2.24 mmol L,回收率值在 90.8 至 96.0%之间。ME-CD 首次展示了用于测定采出水中环烷酸的令人满意的分析性能,这对石油或石油工业的调查很有用。