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研究北极沉积物中挥发性甲基硅氧烷的存在和持久性。

Investigating the presence and persistence of volatile methylsiloxanes in Arctic sediments.

机构信息

Department of Environmental Science and Analytical Chemistry, ACES, Stockholm University, Svante Arrhenius väg 8, SE-114 18 Stockholm, Sweden.

出版信息

Environ Sci Process Impacts. 2020 Apr 29;22(4):908-917. doi: 10.1039/c9em00455f.

Abstract

Volatile methylsiloxanes (VMS) have been identified as contaminants of emerging concern in aquatic systems. Here, we report on the presence of VMS in sediment and wastewater from Arctic regions in 2014 to 2016 and model their persistence in Adventfjorden in Longyearbyen, Svalbard. Total concentrations of VMS in sediment were dominated by D4 and D5 and ranged from 0.0024 to 1.7 ng g-1 at Svalbard (Longyearbyen), from 4.0 to 43 ng g-1 in Greenland (Nuuk) and from 0.19 to 21 ng g-1 in the Canadian Archipelago. Concentrations in wastewater samples from Svalbard ranged from 12 to 156 ng L-1. Large variability in reported values of the partition ratio between organic carbon and water (KOC) and enthalpy of sorption (ΔHOC; often estimated from enthalpy of phase change between octanol and water, ΔHOW) of VMS has resulted in high uncertainty in evaluating persistence in aquatic systems. We evaluated previously reported KOC and ΔHOC values from the literature in predicting measured VMS concentrations in sediment and wastewater in scenarios using a fugacity-based multimedia model for VMS concentrations in Svalbard. We tested two different model scenarios: (1) KOC and ΔHOW measurements for three cyclic VMS previously reported by Kozerski et al. (Environ. Toxicol. Chem., 2014, 33, 1937-1945) and Xu and Kropscott (Environ. Chem., 2014, 33, 2702-2710) and (2) the KOC and ΔHOC measurements from Panagopoulos et al. (Environ. Sci. Technol., 2015, 49, 12161-12168 and Environ. Sci. Technol. Lett., 2017, 4(6), 240-245). Concentrations of VMS in sediment predicted from concentrations in wastewater in scenario 2 were in good agreement with measured concentrations, whereas in scenario 1, predicted concentrations were 2 to 4 orders of magnitude lower. Such large discrepancies indicate that the differences in the predicted concentrations are more likely to be attributed to KOC and ΔHOC than to uncertainty in environmental parameters or emission rates.

摘要

挥发性甲基硅氧烷 (VMS) 已被确定为水生系统中新兴关注的污染物。在这里,我们报告了 2014 年至 2016 年北极地区沉积物和废水中 VMS 的存在情况,并对斯瓦尔巴群岛朗伊尔城的 Adventfjorden 中 VMS 的持久性进行了建模。沉积物中 VMS 的总浓度主要由 D4 和 D5 主导,在斯瓦尔巴群岛(朗伊尔城)的浓度范围为 0.0024 至 1.7ng/g,在格陵兰岛(努克)的浓度范围为 4.0 至 43ng/g,在加拿大群岛的浓度范围为 0.19 至 21ng/g。斯瓦尔巴群岛废水样品中的浓度范围为 12 至 156ng/L。VMS 的有机碳与水之间的分配系数 (KOC) 和吸附焓 (ΔHOC;通常从辛醇与水之间的相变焓,ΔHOW 估算) 的报告值存在很大差异,导致在评估水生系统中的持久性方面存在很高的不确定性。我们评估了文献中以前报告的 KOC 和 ΔHOC 值,以预测使用基于逸度的 VMS 浓度多介质模型在斯瓦尔巴群岛中测量的沉积物和废水中 VMS 浓度。我们测试了两种不同的模型情景:(1)Kozerski 等人以前报道的三种环状 VMS 的 KOC 和 ΔHOW 测量值(Environ. Toxicol. Chem.,2014,33,1937-1945)和 Xu 和 Kropscott(Environ. Chem.,2014,33,2702-2710),以及 (2)Panagopoulos 等人的 KOC 和 ΔHOC 测量值(Environ. Sci. Technol.,2015,49,12161-12168 和 Environ. Sci. Technol. Lett.,2017,4(6),240-245)。情景 2 中从废水中预测的沉积物中 VMS 浓度与实测浓度吻合较好,而情景 1 中预测的浓度低 2 至 4 个数量级。如此大的差异表明,预测浓度的差异更可能归因于 KOC 和 ΔHOC,而不是环境参数或排放率的不确定性。

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