Polidori Andrea, Arhami Mohammad, Sioutas Constantinos, Delfino Ralph J, Allen Ryan
Department of Civil and Environmental Engineering, University of Southern California, Los Angeles, CA 90089, USA.
J Air Waste Manag Assoc. 2007 Mar;57(3):366-79. doi: 10.1080/10473289.2007.10465339.
Hourly indoor and outdoor fine particulate matter (PM2.5), organic and elemental carbon (OC and EC, respectively), particle number (PN), ozone (O3), carbon monoxide (CO), and nitrogen oxide (NOx) concentrations were measured at two different retirement communities in the Los Angeles, CA, area as part of the Cardiovascular Health and Air Pollution Study. Site A (group 1 [G1]) was operated from July 6 to August 20, 2005 (phase 1 [P1]) and from October 19 to December 10, 2005 (P2), whereas site B (group 2 [G2]) was operated from August 24 to October 15, 2005 (P1), and from January 4 to February 18, 2006 (P2). Overall, the magnitude of indoor and outdoor measurements was similar, probably because of the major influence of outdoor sources on indoor particle and gas levels. However, G2 showed a substantial increase in indoor OC, PN, and PM2.5 between 6:00 and 9:00 a.m., probably from cooking. The contributions of primary and secondary OC (SOA) to measured outdoor OC were estimated from collected OC and EC concentrations using EC as a tracer of primary combustion-generated OC (i.e., "EC tracer method"). The study average outdoor SOA accounted for 40% of outdoor particulate OC (40-45% in the summer and 32-40% in the winter). Air exchange rates (hr(-1)) and infiltration factors (Finf; dimensionless) at each site were also determined. Estimated Finf and measured particle concentrations were then used in a single compartment mass balance model to assess the contributions of indoor and/or outdoor sources to measured indoor OC, EC, PM2.5, and PN. The average percentage contributions of indoor SOA of outdoor origin to measured indoor OC were approximately 35% (during G1P1 and G1P2) and approximately 45% (for G2P1 and G2P2). On average, 36% (G2P1) to 44% (G1P1) of measured indoor OC was composed of outdoor-generated primary OC.
作为心血管健康与空气污染研究的一部分,在加利福尼亚州洛杉矶地区的两个不同退休社区,对每小时的室内和室外细颗粒物(PM2.5)、有机碳和元素碳(分别为OC和EC)、颗粒物数量(PN)、臭氧(O3)、一氧化碳(CO)以及氮氧化物(NOx)浓度进行了测量。A站点(第1组[G1])在2005年7月6日至8月20日(第1阶段[P1])以及2005年10月19日至12月10日(P2)期间运行,而B站点(第2组[G2])在2005年8月24日至10月15日(P1)以及2006年1月4日至2月18日(P2)期间运行。总体而言,室内和室外测量值的大小相似,这可能是由于室外源对室内颗粒物和气体水平的主要影响。然而,G2组在上午6:00至9:00之间室内OC、PN和PM2.5大幅增加,可能是由于烹饪所致。利用收集到的OC和EC浓度,以EC作为一次燃烧产生的OC的示踪剂(即“EC示踪法”),估算了一次OC和二次OC(SOA)对测量的室外OC的贡献。该研究中室外SOA的平均值占室外颗粒物OC的40%(夏季为40 - 45%,冬季为32 - 40%)。还确定了每个站点的空气交换率(小时^(-1))和渗透因子(Finf;无量纲)。然后,将估算的Finf和测量的颗粒物浓度用于单室质量平衡模型,以评估室内和/或室外源对测量的室内OC、EC、PM².⁵和PN的贡献。室外来源的室内SOA对测量的室内OC的平均贡献百分比约为35%(在G1P1和G1P2期间)和约45%(对于G2P1和G2P2)。测量的室内OC平均有36%(G2P1)至44%(G1P1)由室外产生的一次OC组成。