Balducci Catia, Cecinato Angelo, Paolini Valerio, Guerriero Ettore, Perilli Mattia, Romagnoli Paola, Tortorella Carmela, Nacci Renato Michele, Giove Aldo, Febo Antonio
National Research Council of Italy, Institute of Atmospheric Pollution Research (CNR-IIA), Monterotondo, RM, Italy.
National Research Council of Italy, Institute of Atmospheric Pollution Research (CNR-IIA), Monterotondo, RM, Italy.
Chemosphere. 2017 Dec;189:330-339. doi: 10.1016/j.chemosphere.2017.09.062. Epub 2017 Sep 15.
The artifacts induced by oxidative degradation and volatilization were assessed with regards to determination of particulate atmospheric PAHs collected at low volume conditions (2.3 m h) according to the EU Reference Method EN 12341:2014. In order to evaluate the oxidative degradation, PAH measures carried out through collecting airborne particulate with and without ozone denuders were examined. Simultaneously, the influence of volatilization was investigated by comparing concentrations of PAHs in particulate samples collected over 24-h and 12-h using conventional instruments. Summer and winter/spring campaigns were carried out in order to assess the influence of environmental contour on the artifact processes. Oxidative degradation led to a general decrease of PAH concentrations in both periods; in particular, the highest losses were observed for benzo[a]pyrene and perylene reaching, in average, ca. 20%. In the summer, the effect of volatilization exceeded that of oxidative degradation for light PAHs up to benzo[e]pyrene. In the winter/spring time, the influence of both artifact typologies could be mitigated by splitting the normal 24-h collection interval starting at midnight into two 12-h intervals. A mitigation of the losses could even be obtained by fixing the start time sampling fixed at noon or in the first hours of the day. Finally, the feasibility of collecting PAHs through prolonged sampling (>1 month) at the flow rate of 1.1 L min was preliminarily investigated. Results indicated that this approach is unsuitable for minimizing the oxidative artifacts.
根据欧盟参考方法EN 12341:2014,针对在低流量条件(2.3米/小时)下采集的大气颗粒物多环芳烃的测定,对氧化降解和挥发所导致的假象进行了评估。为了评估氧化降解情况,对通过使用和不使用臭氧捕集器采集空气颗粒物所进行的多环芳烃测量进行了检查。同时,通过比较使用传统仪器在24小时和12小时内采集的颗粒物样品中多环芳烃的浓度,研究了挥发的影响。开展了夏季以及冬季/春季的采样活动,以评估环境条件对假象形成过程的影响。氧化降解在两个时期均导致多环芳烃浓度普遍下降;特别是,苯并[a]芘和苝的损失最为严重,平均达到约20%。在夏季,对于直至苯并[e]芘的轻质多环芳烃,挥发的影响超过了氧化降解。在冬季/春季,通过将从午夜开始的正常24小时采集间隔分为两个12小时间隔,可以减轻这两种假象类型的影响。甚至通过将采样开始时间固定在中午或一天的最初几个小时,可以进一步减轻损失。最后,初步研究了以1.1升/分钟的流速进行长时间采样(>1个月)来采集多环芳烃的可行性。结果表明,这种方法不适用于最小化氧化假象。