Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, P/Bag 3, WITS, Johannesburg, 2050, South Africa.
Environ Monit Assess. 2014 Sep;186(9):5639-53. doi: 10.1007/s10661-014-3809-3. Epub 2014 May 29.
In this study, the semipermeable membrane device (SPMD) passive samplers were used to determine freely dissolved concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in selected water bodies situated in and around Johannesburg City, South Africa. The devices were deployed for 14 days at each sampling site in spring and summer of 2011. Time weighted average (TWA) concentrations of the water-borne contaminants were calculated from the amounts of analytes accumulated in the passive samplers. In the area of interest, concentrations of analytes in water ranged from 33.5 to 126.8 ng l(-1) for PAHs, from 20.9 to 120.9 pg l(-1) for PCBs and from 0.2 to 36.9 ng l(-1) for OCPs. Chlorinated pesticides were mainly composed of hexachlorocyclohexanes (HCHs) (0.15-36.9 ng l(-1)) and dichlorodiphenyltrichloromethane (DDT) with its metabolites (0.03-0.55 ng l(-1)). By applying diagnostic ratios of certain PAHs, identification of possible sources of the contaminants in the various sampling sites was performed. These ratios were generally inclined towards pyrogenic sources of pollution by PAHs in all study sites except in the Centurion River (CR), Centurion Lake (CL) and Airport River (AUP) that indicated petrogenic origins. This study highlights further need to map up the temporal and spatial variations of these POPs using passive samplers.
本研究采用半渗透膜装置(SPMD)被动采样器,测定了南非约翰内斯堡市及其周边地区选定水体中多环芳烃(PAHs)、多氯联苯(PCBs)和有机氯农药(OCPs)的自由溶解浓度。2011 年春、夏季,每个采样点的装置部署时间为 14 天。从被动采样器中累积的分析物的量计算出水中污染物的时间加权平均(TWA)浓度。在所研究的区域,水中分析物的浓度范围为:PAHs 为 33.5 至 126.8ng/L,PCBs 为 20.9 至 120.9pg/L,OCPs 为 0.2 至 36.9ng/L。氯化农药主要由六氯环己烷(HCHs)(0.15-36.9ng/L)和滴滴涕(DDT)及其代谢物(0.03-0.55ng/L)组成。通过应用某些 PAHs 的诊断比值,可以确定各采样点中污染物的可能来源。除 Centurion 河(CR)、Centurion 湖(CL)和机场河(AUP)外,所有研究地点的这些比值普遍倾向于 PAHs 的热成因污染源,表明其来源于石油。本研究进一步强调需要利用被动采样器来绘制这些持久性有机污染物的时空变化图。