Zhang Xiongfei, Qi Anan, Wang Pengcheng, Huang Qi, Zhao Tong, Yan Caiqing, Yang Lingxiao, Wang Wenxing
Environment Research Institute, Shandong University, Qingdao 266237, China.
Jiangsu Collaborative Innovation Center for Climate Change, Nanjing 210093, China.
Toxics. 2023 Jun 17;11(6):540. doi: 10.3390/toxics11060540.
The knowledge of the spatial distribution, sources, and air-soil exchange of polycyclic aromatic compounds (PACs) in an oilfield area is essential to the development of effective control practices of PAC pollution. In this study, 48 passive air samples and 24 soil samples were collected during 2018-2019 in seven functional areas (e.g., urban, oil field, suburban, industrial, agricultural, near pump units, and background) in the Yellow River Delta (YRD) where the Shengli Oilfield is located, and 18 parent polycyclic aromatic hydrocarbons (PAHs) and five alkylated-PAHs (APAHs) were analyzed from all the air and soil samples. The ΣPAHs in the air and soil ranged from 2.26 to 135.83 ng/m and 33.96 to 408.94 ng/g, while the ΣAPAHs in the atmosphere and soil ranged from 0.04 to 16.31 ng/m and 6.39 to 211.86 ng/g, respectively. There was a downward trend of atmospheric ΣPAH concentrations with increasing the distance from the urban area, while both ΣPAH and ΣAPAH concentrations in the soil decreased with distance from the oilfield area. PMF analyses show that for atmospheric PACs, coal/biomass combustion was the main contributor in urban, suburban, and agricultural areas, while crude production and processing source contributes more in the industrial and oilfield area. For PACs in soil, densely populated areas (industrial, urban, and suburban) are more affected by traffic sources, while oilfield and near-pump unit areas are under the impact of oil spills. The fugacity fraction (ff) results indicated that the soil generally emitted low-molecular-weight PAHs and APAHs and act as a sink for high-molecular-weight PAHs. The incremental lifetime cancer risk (ILCR) of Σ(PAH+APAH) in both the air and soil, were below the threshold (≤10) set by the US EPA.
了解油田区域中多环芳烃化合物(PACs)的空间分布、来源及气-土交换情况,对于制定有效的PAC污染控制措施至关重要。本研究于2018 - 2019年期间,在胜利油田所在的黄河三角洲(YRD)的七个功能区(如城区、油田、郊区、工业区、农业区、抽油机附近区域和背景区域)采集了48个被动空气样本和24个土壤样本,并对所有空气和土壤样本中的18种母体多环芳烃(PAHs)和5种烷基化多环芳烃(APAHs)进行了分析。空气和土壤中的ΣPAHs含量范围分别为2.26至135.83 ng/m³和33.96至408.94 ng/g,而大气和土壤中的ΣAPAHs含量范围分别为0.04至16.31 ng/m³和6.39至211.86 ng/g。大气中ΣPAH浓度随距城区距离增加呈下降趋势,而土壤中ΣPAH和ΣAPAH浓度均随距油田区域距离增加而降低。PMF分析表明,对于大气中的PACs,煤炭/生物质燃烧是城区、郊区和农业区的主要贡献源,而原油生产和加工源在工业区和油田区域的贡献更大。对于土壤中的PACs,人口密集区域(工业区、城区和郊区)受交通源影响更大,而油田和抽油机附近区域则受到石油泄漏的影响。逸度分数(ff)结果表明,土壤通常排放低分子量的PAHs和APAHs,并作为高分子量PAHs的汇。空气和土壤中Σ(PAH + APAH)的增量终生癌症风险(ILCR)均低于美国环保署设定的阈值(≤10)。