Almendral María-Jesús, Alonso Angel, Fuentes María-Socorro
Departamento de Química Analítica, Nutrición y Bromatología, Faculty of Chemistry, University of Salamanca, Plaza de la Merced s/n, E-37008, Salamanca, Spain.
J Environ Monit. 2009 Jul;11(7):1381-8. doi: 10.1039/b900773c. Epub 2009 May 26.
The bromate ion has been identified as an inorganic disinfection by-product (DPB) in water subjected to purification treatment. Its presence arises from the application of oxidation processes to water containing bromide through the action of oxidant agents such as the ozone used in ozonation processes. This ion has been identified as a possible carcinogen by the U.S. Environmental Protection Agency, which recommends a maximum concentration of 10 microgL(-1). The literature reports a broad range of methods for the analysis of bromate in water, among which ion chromatography is the one most widely used, with different detection systems. However, most of the methods described to date require state-of-the-art technology and costly instrumentation, such that they are not readily adaptable to routine analyses. The present work reports a procedure for the spectrophotometric determination of bromate based on the bromination reaction of 3-3' dimethoxybenzidine, o-dianisidine (ODA). The reaction is based on the formation of Br2 in the presence of excess bromide and the later bromination of ODA, generating a product that absorbs at 450 nm. The procedure was set up with Flow Injection Analysis and allows the determination of the analyte in the 8 microg L(-1)-3.3 mg L(-1) range, with a detection limit of 6.0 microg L(-1) and relative standard deviations (n=12, [BrO3-]=8.0 and 30.0 microg L(-1)) of 4.8% and 2.9%, respectively. The determination rate was 10-11 samples/hour.
溴酸根离子已被确认为经过净化处理的水中的一种无机消毒副产物(DPB)。其存在源于通过氧化剂(如臭氧化过程中使用的臭氧)对含溴水进行氧化处理。该离子已被美国环境保护局确定为可能的致癌物,其建议的最大浓度为10微克/升。文献报道了多种分析水中溴酸根的方法,其中离子色谱法是使用最广泛的,具有不同的检测系统。然而,迄今为止所描述的大多数方法都需要先进的技术和昂贵的仪器,因此它们不易适用于常规分析。本工作报道了一种基于3,3'-二甲氧基联苯胺(邻联茴香胺,ODA)溴化反应的分光光度法测定溴酸根的方法。该反应基于在过量溴化物存在下生成Br2,随后ODA被溴化,生成一种在450nm处有吸收的产物。该方法采用流动注射分析建立,可测定8微克/升 - 3.3毫克/升范围内的分析物,检测限为6.0微克/升,相对标准偏差(n = 12,[BrO3-]=8.0和30.0微克/升)分别为4.8%和2.9%。测定速率为每小时10 - 11个样品。