Simple HPLC–UV Analysis of Phenol and Its Related Compounds in Tap Water after Pre-Column Derivatization with 4-Nitrobenzoyl Chloride

Y. Higashi
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引用次数: 8

Abstract

The purpose of this study is to develop an HPLC-UV (280 nm) method for simultaneous determination of phenol, five chlorophenols (2-chlorophenol, 4-chlorophenol, 2,4-dichlorophenol, 2,6-dichlorophenol, and 2,4,6-trichlorophenol), and three phenylphenols (2-phenylphenol, 3-phenylphenol, and 4-phenylphenol) in tap water after pre-column derivatization with 4-nitrobenzoyl chloride. Standard curves were obtained after derivatization with 4-nitrobenzoyl chloride in borate buffer (pH 8.5) at 50°C for 1 min. The nine 4-nitrobenzoyl derivatives were well separated in less than 15 min on a Cholester column. Calibration plots were linear in the range of 0.02 ~ 0.12 to 0.9 mg/L, with r2 values ≥0.9928, for all compounds. The lower limits of detection were 0.006 to 0.05 mg/L. The coefficients of variation were less than 12.0%. The recovery values from tap water spiked with a standard mixture of test compounds were satisfactory. While the levels of phenol, five chlorophenols, and three phenylphenols in tap water were below the lower limit of determination, our method is expected to be useful for monitoring and/or identifying environmental water samples that are contaminated with these compounds, i.e., for assessing compliance with the official guidelines of the World Health Organization.
4-硝基苯甲酰氯柱前衍生自来水中苯酚及其相关化合物的HPLC-UV分析
本研究建立了一种HPLC-UV (280 nm)同时测定自来水中酚、5种氯酚(2-氯酚、4-氯酚、2,4-二氯酚、2,4,6-三氯酚)和3种苯基酚(2-苯基酚、3-苯基酚和4-苯基酚)的柱前衍生法。在硼酸缓冲液(pH 8.5)中,用4-硝基苯甲酰氯在50℃下衍生1 min,得到标准曲线。在Cholester柱上,9个4-硝基苯甲酰衍生物在不到15 min的时间内得到了很好的分离。在0.02 ~ 0.12 ~ 0.9 mg/L范围内呈线性关系,r2值≥0.9928。检测下限为0.006 ~ 0.05 mg/L。变异系数均小于12.0%。从自来水中加入标准混合物的回收率是令人满意的。虽然自来水中苯酚、五种氯酚和三种苯基酚的含量低于测定下限,但我们的方法有望用于监测和/或确定受这些化合物污染的环境水样,即用于评估是否符合世界卫生组织的官方准则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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