Wang Ping, Wang Zhong-Min, Wagner Jeff, Kumagai Kazukiyo
Environmental Health Laboratory Branch, Center for Laboratory Sciences, California Department of Public Health, Richmond, CA 94804, USA.
Environmental Health Laboratory Branch, Center for Laboratory Sciences, California Department of Public Health, Richmond, CA 94804, USA.
J Chromatogr A. 2025 Mar 15;1744:465689. doi: 10.1016/j.chroma.2025.465689. Epub 2025 Jan 16.
A solvent-free, thermal extraction method for analysis of polycyclic aromatic hydrocarbons (PAHs) in gas phase airborne samples was developed. A fully automated thermal desorber (TD) coupled with highly selective and sensitive gas chromatography-tandem mass spectrometry (GC-MS/MS) was used to determine the concentration of trace level PAHs. Air sampling was conducted to tune the sampling and analytical conditions. Various instrument operating parameters such as sorbent tube desorption temperature/time, cold trap desorption temperature/time, outlet split ratio, tube storage stability, as well as air sampling flow rate and time were tested to optimize the analytical conditions. Method performance showed linearity in broad range (0.01 to 10 ng) with regression coefficients of external calibration curves (R) >0.998 for all targeted PAHs. Method detection limit (MDL) was between 0.01-0.05 ng per tube. The method precision (<20 %) and accuracy were also satisfactory, obtaining quantitative recoveries (mean values between 80 and 120 %). The method has been applied for both outdoor and indoor air analysis. Small volume of air sample (<144 L) was sufficient for the PAH analysis. Naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, anthracene, fluoranthene, acenaphthene, fluorene, pyrene, and acenaphthylene are the primary PAHs in the gas phase for both indoor and outdoor air. Naphthalene and its two methylated compounds: 1-methylnaphthalene and 2-methylnaphthalene accounted for 47.7 % and 81.7 % of the total gas phase PAHs for outdoor and indoor, respectively. Using thermal extraction instead of organic solvent extraction for sample pretreatment makes the method sustainable and in consonance with the principles of green chemistry. No solvent and time-consuming extract step are needed. The method greatly improved the analytical process with a fully automated TD-GC-MS/MS instrument.
开发了一种用于分析气相空气传播样品中多环芳烃(PAHs)的无溶剂热萃取方法。使用全自动热解吸仪(TD)与高选择性和高灵敏度的气相色谱-串联质谱(GC-MS/MS)联用,以测定痕量水平PAHs的浓度。进行空气采样以调整采样和分析条件。测试了各种仪器操作参数,如吸附剂管解吸温度/时间、冷阱解吸温度/时间、出口分流比、管储存稳定性以及空气采样流速和时间,以优化分析条件。方法性能在宽范围(0.01至10 ng)内呈线性,所有目标PAHs的外标校准曲线回归系数(R)>0.998。方法检测限(MDL)为每管0.01 - 0.05 ng。方法精密度(<20%)和准确度也令人满意,获得定量回收率(平均值在80%至120%之间)。该方法已应用于室外和室内空气分析。小体积空气样品(<144 L)足以进行PAH分析。萘、1-甲基萘、2-甲基萘、蒽、荧蒽、苊、芴、芘和苊烯是室内和室外空气中气相中的主要PAHs。萘及其两种甲基化化合物1-甲基萘和2-甲基萘分别占室外和室内气相PAHs总量的47.7%和81.7%。使用热萃取代替有机溶剂萃取进行样品预处理,使该方法具有可持续性,符合绿色化学原则。无需溶剂和耗时的萃取步骤。该方法通过全自动TD-GC-MS/MS仪器极大地改进了分析过程。