Erustes J A, Andrade-Eiroa A, Cladera A, Forteza R, Cerdà V
Department of Chemistry, University of Balearic Islands, E-07071 Palma de Mallorca, Spain.
Analyst. 2001 Apr;126(4):451-6. doi: 10.1039/b010129j.
A methodology for the analysis of drinking water for one of the most potent carcinogenic agents known; benzo[a]pyrene (BaP), in the presence of other interfering PAHs is presented. The methodology described is based on the sequential injection analysis of the sample on to a microcolumn (containing 5 mg of C18) where extraction and preconcentration of BaP takes place, followed by elution of BaP with 1 ml of 1,4-dioxane and subsequent detection by using variable angle fluorescence. The advantages of the method include the small amount of stationary phase employed together with the possibility of re-using the phase in order to carry out a large number of injections without the need for column re-packing. Also noteworthy is the small volume of 1,4-dioxane used to elute the BaP retained on the column and the small sample volumes required (9-10 ml) for achieving detection limits at the ng l-1 level. Thus, a methodology for BaP determination is obtained which complies with the requirements of the 98/83/EC Directive which fixes a maximum admissible concentration for this pollutant in waters for public consumption of 10 ng l-1. The variable angle spectra obtained are further processed by means of the multiple linear regression technique. The detection limit for BaP is 2.5 ng l-1, and the linear range is between 7.5 and 280 ng l-1.
本文介绍了一种用于分析饮用水中已知最强致癌物质之一苯并[a]芘(BaP)的方法,该方法适用于存在其他干扰性多环芳烃的情况。所描述的方法基于将样品顺序注入微柱(含有5毫克C18),在该微柱中进行BaP的萃取和预浓缩,然后用1毫升1,4 - 二氧六环洗脱BaP,随后使用可变角度荧光进行检测。该方法的优点包括使用的固定相量少,并且有可能重复使用该固定相以进行大量进样而无需重新填充色谱柱。同样值得注意的是,用于洗脱保留在柱上的BaP的1,4 - 二氧六环体积小,以及达到纳克/升水平的检测限所需的样品体积小(9 - 10毫升)。因此,获得了一种用于BaP测定的方法,该方法符合98/83/EC指令的要求,该指令规定了供公众消费的水中该污染物的最大允许浓度为10纳克/升。通过多元线性回归技术对获得的可变角度光谱进行进一步处理。BaP的检测限为2.5纳克/升,线性范围在7.5至280纳克/升之间。