Nakamura S, Takino M, Daishima S
Yokogawa Analytical Systems Inc., 2-11-13 Nakacho, Musashino-shi, Tokyo 180-0006, Japan.
Analyst. 2001 Jun;126(6):835-9. doi: 10.1039/b101194o.
A method for the trace level determination of 11 phenols as pentafluorobenzyl (PFB) derivatives by gas chromatography-mass spectrometry (GC-MS) with negative-ion chemical ionization (NICI) is described. First, the conditions for the PFB derivatisation of phenols were optimized and were found to be reaction temperature 80 degrees C and reaction time 5 h. Second, the detection limits using selected ion monitoring (SIM) were compared between trimethylsilylated (TMS) derivatives in the electron ionization (EI) mode and PFB derivatives in the NICI mode. The responses for the PFB derivatives in the NICI mode were 3.3-61 times higher than those of the TMS derivatives in the EI mode. The instrumental detection limits using NICI-SIM ranged from 2.6 to 290 fg. This method was applied to the analysis of phenols in river water using solid-phase extraction. The recoveries of the phenols from a river water sample spiked with standards at 100 ng l-1 with 2-chlorophenol, 4-chloro-3-methylphenol and pentachlorophenol and at 1000 ng l-1 with phenol, 2,4-dimethylphenol, 2,4-dichlorophenol, 2-nitrophenol, 2,4,6-trichlorophenol and 4-nitrophenol were 81.2-106.3% (RSD 5.1-8.0%), except for 2-methyl-4,6-dinitrophenol and 2,4-dinitrophenol, for which the recoveries were 5.8 and 4.2%, respectively, because water contained in the acetone eluate interfered with the derivatisation of these compounds with two electrophilic nitro groups.
描述了一种通过气相色谱 - 质谱联用(GC - MS)和负离子化学电离(NICI)测定11种酚类的五氟苄基(PFB)衍生物痕量水平的方法。首先,对酚类的PFB衍生化条件进行了优化,发现反应温度为80℃,反应时间为5小时。其次,比较了在电子电离(EI)模式下三甲基硅烷化(TMS)衍生物和在NICI模式下PFB衍生物使用选择离子监测(SIM)的检测限。NICI模式下PFB衍生物的响应比EI模式下TMS衍生物的响应高3.3 - 61倍。使用NICI - SIM的仪器检测限范围为2.6至290 fg。该方法应用于采用固相萃取分析河水中的酚类。从添加了100 ng l-1的2 - 氯酚、4 - 氯 - 3 - 甲基酚和五氯酚以及1000 ng l-1的苯酚、2,4 - 二甲基酚、2,4 - 二氯酚、2 - 硝基酚、2,4,6 - 三氯酚和4 - 硝基酚标准品的河水样品中回收酚类,回收率为81.2 - 106.3%(相对标准偏差5.1 - 8.0%),但2 - 甲基 - 4,6 - 二硝基酚和2,4 - 二硝基酚除外,其回收率分别为5.8%和4.2%,这是因为丙酮洗脱液中含有的水干扰了这些具有两个亲电硝基的化合物的衍生化。