SOA Key Laboratory for Polar Science, Polar Research Institute of China, Shanghai 200136, China.
J Hazard Mater. 2012 Mar 30;209-210:335-42. doi: 10.1016/j.jhazmat.2012.01.030. Epub 2012 Jan 16.
The multi-matrices samples from snow (n=4), lake water (n=4), surface runoff water (SRW) (n=1) and coastal seawater (n=10) were collected to investigate the spatial distribution and the composition profiles of per- and polyfluoroalkyl substances (PFASs) in Fildes Peninsula, King George Island, Antarctica in 2011. All samples were prepared by solid-phase extraction and analyzed by using high performance liquid chromatography/negative electrospray ionization-tandem mass spectrometry (HPLC/(-)ESI-MS/MS). 14 PFASs in snow, 12 PFASs in lake water, 9 PFASs in SRW and 13 PFASs in coastal seawater were quantified, including C(4), C(7), C(8), C(10) PFSAs, C(4)-C(9), C(11)-C(14), C(16) PFCAs, and FOSA. PFOA was detected in all samples with the highest concentration (15,096 pg/L) in coastal seawater indicating a possible influence of local sewage effluent. High concentration and mostly frequency of PFBA occurred in snow (up to 1112 pg/L), lake water (up to 2670 pg/L) and SRW (1431 pg/L) while detected in the range of method detection limited (MDL) in the coastal seawaters indicate that PFBA is mainly originated from atmospheric dust contamination and also affected by the degradation of their precursors. No geographical differences in PFOS concentrations (n=8, 18 ± 3 pg/L) were measured in all snow and lake water samples also suggests that PFOS could be originated from the degradation of their precursors which can transported by long-range atmospheric route, but in a very low level.
于 2011 年在南极洲乔治王岛菲尔德斯半岛采集了来自雪(n=4)、湖水(n=4)、地表径流水(SRW)(n=1)和近岸海水(n=10)的多矩阵样本,以调查全氟和多氟烷基物质(PFASs)在这些地区的空间分布和组成分布。所有样本均通过固相萃取法制备,并通过高效液相色谱/负离子电喷雾串联质谱法(HPLC/(-)ESI-MS/MS)进行分析。在雪样中定量了 14 种 PFASs、湖水中 12 种、SRW 中 9 种和近岸海水中 13 种,包括 C(4)、C(7)、C(8)、C(10)PFASs、C(4)-C(9)、C(11)-C(14)、C(16)PFCAs 和 FOSA。所有样本中均检测到 PFOA,其浓度最高(15096 pg/L)的样本来自近岸海水,这表明当地污水排放可能对其有影响。在雪(高达 1112 pg/L)、湖水(高达 2670 pg/L)和 SRW(1431 pg/L)中,PFBA 的浓度和出现频率均较高,而在近岸海水中的检测浓度均处于方法检测限(MDL)范围内,这表明 PFBA 主要来源于大气灰尘污染,也受其前体降解的影响。所有雪和湖水样本中 PFOS 浓度(n=8,18 ± 3 pg/L)均无明显地域差异,这也表明 PFOS 可能来源于其前体的降解,这些前体可以通过长距离大气途径传输,但浓度非常低。