Zencak Zdenek, Klanova Jana, Holoubek Ivan, Gustafsson Orjan
Department of Applied Environmental Science (ITM), Stockholm University, 10691 Stockholm, Sweden.
Environ Sci Technol. 2007 Jun 1;41(11):3850-5. doi: 10.1021/es0628957.
Progress in source apportionment of priority combustion-derived atmospheric pollutants can be made by an inverse approach to inventory emissions, namely, receptor-based compound class-specific radiocarbon analysis (CCSRA) of target pollutants. In the present study, CCSRA of the combustion-derived polycyclic aromatic hydrocarbons (PAHs) present in the atmosphere of the countries of the former republic of Yugoslavia was performed. The carbon stable isotope composition (delta13C) of PAHs varied between -27.68 and -27.19 per thousand, whereas delta14C values ranged from -568 per thousand for PAHs sampled in Kosovo to -288 per thousand for PAHs sampled in the Sarajevo area. The application of an isotopic mass balance model to these delta14C data revealed a significant contribution (35-65%) from the combustion of non-fossil material to the atmospheric PAH pollution, even in urban and industrialized areas. Furthermore, consistency was observed between the isotopic composition of PAHs obtained by high-volume sampling and those collected by passive sampling. This encourages the use of passive samplers for CCSRA applications. This marks the first time that a CCSRA investigation could be executed on a geographically wide scale, providing a quantitative field-based source apportionment, which points out that also non-fossil combustion processes should be targeted for remedial action.
通过对排放清单采用反向方法,即对目标污染物进行基于受体的特定化合物类别放射性碳分析(CCSRA),可以在优先燃烧源大气污染物的源解析方面取得进展。在本研究中,对前南斯拉夫各国大气中存在的燃烧源多环芳烃(PAHs)进行了CCSRA分析。PAHs的碳稳定同位素组成(δ13C)在千分之-27.68至-27.19之间变化,而δ14C值范围从科索沃采样的PAHs的千分之-568到萨拉热窝地区采样的PAHs的千分之-288。将同位素质量平衡模型应用于这些δ14C数据表明,即使在城市和工业化地区,非化石材料燃烧对大气PAH污染也有显著贡献(35-65%)。此外,在通过大容量采样获得的PAHs同位素组成与通过被动采样收集的PAHs同位素组成之间观察到一致性。这鼓励在CCSRA应用中使用被动采样器。这标志着首次能够在地理范围广泛的尺度上开展CCSRA调查,提供基于实地的定量源解析,指出非化石燃烧过程也应作为补救行动的目标。