Polo Maria, Llompart Maria, Garcia-Jares Carmen, Gomez-Noya Guadalupe, Bollain Maria-Herminia, Cela Rafael
Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Química, Instituto de Investigación y Análisis Alimentario, Universidad de Santiago de Compostela, E-15782 Santiago de Compostela, Spain.
J Chromatogr A. 2006 Aug 18;1124(1-2):11-21. doi: 10.1016/j.chroma.2006.03.047. Epub 2006 Apr 5.
A solid-phase microextraction (SPME) method for the ultra-trace determination of brominated phenols in aqueous samples has been developed and is reported for the first time to the best of our knowledge. 3,5,3',5'-tetrabromobisphenol A (TBBPA), the most widely used brominated flame retardant, and other phenolic flame retardants in commercial use, such as 2,4-dibromophenol (2,4-DBP), 2,4,6-tribromophenol (TBP) and pentabromophenol (PBP) have been included as target analytes. The analytical procedure involves the in situ acetylation-SPME and gas chromatography-mass spectrometry (GC-MS) determination of the target analytes. A multi-factor categorical experimental design was created to study the main parameters affecting the extraction efficiency, allowing also the evaluation of interaction effects between factors. The factors studied were type of fiber, extraction mode, exposing the fiber directly into the sample (DSPME) or into the headspace over the sample (HSSPME), and extraction temperature. Carboxen-polydimethylsiloxane (CAR-PDMS) fiber appeared to be the most suitable of the five fibers tested for the extraction of most compounds, excluding PBP and TBBPA for which polydimethylsiloxane (PDMS) was the most efficient coating. The highest response was achieved for both fibers sampling in headspace mode at 100 degrees C. In order to test the linearity of the method, calibration studies were performed with both CAR-PDMS and PDMS coatings. For both fibers, the method was linear in a range of 2 orders of magnitude, giving relative standard deviation (RSD%) below 10% for most compounds and detection limits at the low pg/mL level. In addition, the feasibility of the method for simultaneous determination of chlorinated and brominated phenols was studied. Finally, the method was applied to several real samples including tap water and effluent and influent waste water samples from an urban treatment plant, in which several phenolic compounds, such as phenol, methylphenols and chlorophenols, could be detected and quantified.
据我们所知,首次开发并报道了一种用于超痕量测定水样中溴化酚的固相微萃取(SPME)方法。3,5,3',5'-四溴双酚A(TBBPA)是使用最广泛的溴化阻燃剂,以及其他商业用途的酚类阻燃剂,如2,4-二溴苯酚(2,4-DBP)、2,4,6-三溴苯酚(TBP)和五溴苯酚(PBP)已被列为目标分析物。分析程序包括目标分析物的原位乙酰化-SPME和气相色谱-质谱(GC-MS)测定。创建了多因素分类实验设计来研究影响萃取效率的主要参数,同时还能评估因素之间的相互作用效应。所研究的因素包括纤维类型、萃取模式,即将纤维直接暴露于样品中(直接浸入式固相微萃取,DSPME)或样品上方的顶空中(顶空固相微萃取,HSSPME),以及萃取温度。对于大多数化合物的萃取,在测试的五种纤维中,Carboxen-聚二甲基硅氧烷(CAR-PDMS)纤维似乎是最合适的,但PBP和TBBPA除外,对于它们,聚二甲基硅氧烷(PDMS)是最有效的涂层。两种纤维在100℃顶空模式下采样时均获得了最高响应。为了测试该方法的线性,使用CAR-PDMS和PDMS涂层进行了校准研究。对于两种纤维,该方法在2个数量级范围内呈线性,大多数化合物的相对标准偏差(RSD%)低于10%,检测限在低pg/mL水平。此外,研究了该方法同时测定氯代酚和溴代酚的可行性。最后,该方法应用于几个实际样品,包括自来水、城市污水处理厂的出水和进水废水样品,其中可以检测和定量多种酚类化合物,如苯酚、甲基苯酚和氯苯酚。