Wei Chong, Bandowe Benjamin A Musa, Han Yongming, Cao Junji, Zhan Changlin, Wilcke Wolfgang
Key Laboratory of Aerosol Chemistry & Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi'an 710061, China; Geographic Institute, University of Berne, Hallerstrasse 12, 3012 Berne, Switzerland; State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi'an 710061, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Geographic Institute, University of Berne, Hallerstrasse 12, 3012 Berne, Switzerland.
Chemosphere. 2015 Sep;134:512-20. doi: 10.1016/j.chemosphere.2014.11.052. Epub 2014 Dec 24.
Urban road dusts are carriers of polycyclic aromatic compounds (PACs) and are therefore considered to be a major source of contamination of other environmental compartments and a source of exposure to PACs for urban populations. We determined the occurrence, composition pattern and sources of several PACs (29 alkyl- and parent-PAHs, 15 oxygenated-PAHs (OPAHs), 4 azaarenes (AZAs), and 11 nitrated-PAHs (NPAHs)) in twenty urban road dusts and six suburban surface soils (0-5cm) from Xi'an, central China. The average concentrations of ∑29PAHs, ∑4AZAs, ∑15OPAHs, and ∑11NPAHs were 15767, 673, 4754, and 885 n gg(-1) in road dusts and 2067, 784, 854, and 118 ng g(-1) in surface soils, respectively. The concentrations of most individual PACs were higher in street dusts than suburban soils, particularly for PACs with molecular weight>192 g mol(-1). The enrichment factors of individual PACs were significantly positively correlated with log KOA and log KOW, indicating an increasing deposition and co-sorption of the PACs in urban dusts with decreasing volatility and increasing hydrophobicity. Significant correlations between the concentrations of individual and sum of PACs, carbon fractions (soot and char), and source-characteristic PACs (combustion-derived PAHs and retene, etc.), indicated that PAHs, OPAHs and AZAs were mostly directly emitted from combustion activities and had similar post-emission fates, but NPAHs were possibly more intensely photolyzed after deposition as well as being emitted from vehicle exhaust sources. The incremental lifetime cancer risk (ILCR) resulting from exposure to urban dust bound-PACs was higher than 10(-6), indicating a non-negligible cancer risk to residents of Xi'an.
城市道路灰尘是多环芳烃化合物(PACs)的载体,因此被认为是其他环境介质污染的主要来源以及城市居民接触PACs的来源。我们测定了中国中部西安的20份城市道路灰尘和6份郊区表层土壤(0-5厘米)中几种PACs(29种烷基和母体多环芳烃、15种含氧多环芳烃(OPAHs)、4种氮杂芳烃(AZAs)和11种硝化多环芳烃(NPAHs))的存在情况、组成模式和来源。道路灰尘中∑29PAHs、∑4AZAs、∑15OPAHs和∑11NPAHs的平均浓度分别为15767、673、4754和885 ng g(-1),表层土壤中分别为2067、784、854和118 ng g(-1)。大多数单个PACs在街道灰尘中的浓度高于郊区土壤,特别是分子量>192 g mol(-1)的PACs。单个PACs的富集因子与log KOA和log KOW显著正相关,表明随着挥发性降低和疏水性增加,PACs在城市灰尘中的沉积和共吸附增加。单个PACs浓度与PACs总和、碳组分(烟灰和焦炭)以及源特征PACs(燃烧衍生的多环芳烃和惹烯等)之间存在显著相关性,表明多环芳烃、OPAHs和AZAs大多直接来自燃烧活动且具有相似的排放后归宿,但NPAHs可能在沉积后更强烈地发生光解,并且也来自车辆尾气排放源。接触城市灰尘结合的PACs导致的增量终生癌症风险(ILCR)高于10(-6),表明对西安居民的癌症风险不可忽视。