Shan Guoqiang, Yu Mengqi, Yu Shengsong, Zhu Lingyan
Se Pu. 2014 Sep;32(9):942-7. doi: 10.3724/sp.j.1123.2014.05028.
A simple derivatization method followed by high performance liquid chromatography (HPLC) for the analysis of perfluorooctanoic acid (PFOA) was developed. PFOA was firstly derivatized with 3,4-dichloroaniline (DCA) using carbodiimide method. The typical amidate product was characterized by mass spectrometry (MS). It can be detected by a UV detector at maximum absorption wavelength of 255 nm. It was isolated well by methanol/H2O (8/2, v/v) as mobile phase. The DCA derivatization of PFOA in organic or aqueous solutions was opti- mized. The following purification procedures with thin layer chromatography (TLC) and HPLC separations were established. Using external standard method with the authentic PFOA-DCA derivative as standard, the limit of instrumental quantification was found to be 0. 5 mg/L. Good linear correlation coefficients were observed in 0.5-50.0 mg/L. The accuracy of the method was evaluated by the recovery measurements on spiked samples. The recoveries for the spiked samples (1.0 mg/L) in organic phase and aqueous phase were 91.8%-108.7% and 42.1%-53.7%, respectively. Comparing to the reported pre-column derivatization methods followed by HPLC for the determination of PFOA, this method has the advantages of mild reaction conditions, very stable derivative, easy operation, low cost, etc. The method was successfully applied for the quantification of PFOA in photodegradation experiments, and the results were consistent with those determined by LC/MS. Considering the combination of the preconcentration step, it has a potential for the application of the analysis of samples containing relatively low concentrations, such as μg/L levels of PFOA obtained from environmental or scientific experiments.
开发了一种简单的衍生化方法,随后采用高效液相色谱法(HPLC)分析全氟辛酸(PFOA)。首先使用碳二亚胺法将PFOA与3,4-二氯苯胺(DCA)进行衍生化反应。通过质谱(MS)对典型的酰胺产物进行了表征。它可以在255nm的最大吸收波长下由紫外检测器检测到。以甲醇/H2O(8/2,v/v)作为流动相可实现良好的分离。对有机溶液或水溶液中PFOA的DCA衍生化反应进行了优化。建立了随后的薄层色谱(TLC)纯化程序和HPLC分离方法。以真实的PFOA-DCA衍生物为标准采用外标法,仪器定量限为0.5mg/L。在0.5 - 50.0mg/L范围内观察到良好的线性相关系数。通过对加标样品的回收率测定来评估该方法的准确性。有机相和水相中加标样品(1.0mg/L)的回收率分别为91.8% - 108.7%和42.1% - 53.7%。与报道的采用HPLC测定PFOA的柱前衍生化方法相比,该方法具有反应条件温和、衍生物非常稳定、操作简便、成本低等优点。该方法已成功应用于光降解实验中PFOA的定量分析,结果与LC/MS测定结果一致。考虑到预浓缩步骤的结合,它具有应用于分析相对低浓度样品的潜力,例如从环境或科学实验中获得的μg/L水平的PFOA。