413 Choppin Hall, Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70820, USA.
Environ Sci Technol. 2010 Mar 15;44(6):1933-9. doi: 10.1021/es902648t.
Environmentally persistent free radicals (EPFRs) have been shown to form on the surfaces of various types of transition metal-containing particulate matter (PM), and it has been demonstrated they are capable of initiating adverse health impacts. Following sonification and solvent extraction for chemical analysis, they are partially converted to molecular species. Alcoholic solvents extracted the EPFRs with near 100% efficiency, while nonpolar hydrocarbon solvents exhibited <20% efficiency and dichloromethane exhibited 20-55% efficiency. The extracted radicals reacted in solution to form multiple molecular reaction products including catechol, hydroquinone, phenol, chlorinated phenols, dibenzo-p-dioxin, and dibenzofuran. This suggests that EPFRs in environmental samples are indistinguishable from molecular pollutants and are subject to misidentification as molecular adsorbates when traditional extraction and chemical analysis methods are employed. On the basis of these findings, the origin of the toxicity of particulate matter contaminated with toxic organic compounds should be considered for re-evaluation to include the possibility that EPFRs may be a significant contributor, and the impact of some molecular pollutants may have been overestimated.
环境持久性自由基 (EPFRs) 已被证明会在各种类型的含过渡金属的颗粒物 (PM) 表面形成,并且已经证明它们能够引发不良的健康影响。经过超声处理和溶剂萃取进行化学分析后,它们会部分转化为分子物种。醇类溶剂对 EPFRs 的提取效率接近 100%,而非极性碳氢化合物溶剂的提取效率<20%,二氯甲烷的提取效率为 20-55%。提取出的自由基在溶液中反应,形成多种分子反应产物,包括儿茶酚、对苯二酚、苯酚、氯代苯酚、二噁英和呋喃。这表明环境样品中的 EPFRs 与分子污染物无法区分,并且当采用传统的提取和化学分析方法时,它们可能会被错误地识别为分子吸附物。基于这些发现,应重新考虑污染有毒有机化合物的颗粒物的毒性来源,包括 EPFRs 可能是一个重要贡献者的可能性,以及一些分子污染物的影响可能被高估的可能性。