首页> 外文期刊>Analytical chemistry >QUANTITATIVE DETERMINATION OF TOTAL MOLAR CONCENTRATIONS OF BIOACCUMULATABLE ORGANIC MICROPOLLUTANTS IN WATER USING C-18 EMPORE DISK AND MOLAR DETECTION TECHNIQUES
【24h】

QUANTITATIVE DETERMINATION OF TOTAL MOLAR CONCENTRATIONS OF BIOACCUMULATABLE ORGANIC MICROPOLLUTANTS IN WATER USING C-18 EMPORE DISK AND MOLAR DETECTION TECHNIQUES

机译:使用C-18样品碟和摩尔检测技术定量测定水中可生物吸收的有机微污染物的总摩尔浓度。

获取原文
获取原文并翻译 | 示例
       

摘要

A highly sensitive and quantitative group parameter to determine total molar concentrations of organic micropollutants that can bioaccumulate in the lipid phase of aquatic organisms from effluents, surface mater, and drinking water has been developed. C-18 empore disk was used as a surrogate lipid phase, The partition process between water and C-18 empore disk was employed to simulate the bioaccumulation process, After partition extraction of the water sample, the empore disk was extracted with cyclohexane, and total molar concentrations were determined in these extracts using vapor pressure osmometry (VPO) and gas chromatography/mass spectrometry (GC/MS), respectively. Total molar concentrations bioaccumulated in aquatic biota were estimated from the cyclohexane concentrations. Good accuracy for the total molar determination was obtained using VPO, due to the practically constant molar response factors (43.1 +/- 1.7 V/M) for a wide compound range and to excellent additivity of individual compound responses, Satisfying reproducibility (0-8.3%) of VPO was obtained for sample extracts, The detection limit. of VPO in cyclohexane extracts corresponded to 0.60 mM in the lipid phase of aquatic biota, A minimal separation GC/MS system was developed, which enabled highly sensitive and sufficiently accurate total molar determinations. The reproducibility of the GC/MS determination for samples ranged from 0.7 to 22%. The detection limit of GC/MS in cyclohexane extracts corresponded to 0.044 mM in the lipid phase, The determined total molar concentrations in the lipid phase of aquatic biota were in the range of 0.139-168 mM for effluents, 0.26-1.34 mM for surface water systems, and < 0.044 mM for drinking water.
机译:已经开发出一种高度灵敏和定量的组参数,用于确定可以从废水,表面物质和饮用水中在水生生物的脂质相中生物蓄积的有机微量污染物的总摩尔浓度。以C-18孢子盘作为替代脂质相,采用水与C-18孢子盘之间的分配过程模拟生物富集过程,对水样进行分配萃取后,用环己烷萃取该孢子盘,总分别使用蒸气压渗透法(VPO)和气相色谱/质谱(GC / MS)测定这些提取物中的摩尔浓度。根据环己烷浓度估算水生生物区中生物累积的总摩尔浓度。使用VPO可获得良好的总摩尔测定精度,这是因为在宽范围的化合物范围内,摩尔响应因子(43.1 +/- 1.7 V / M)实际上是恒定的,并且各个化​​合物的响应具有出色的可加性,可再现性(0-8.3)对于样品提取物,获得了VPO%)的检测限。环己烷提取物中VPO的含量对应于水生生物脂质相中的0.60 mM,开发了最小分离GC / MS系统,可实现高度灵敏且足够准确的总摩尔测定。 GC / MS测定样品的重现性为0.7%至22%。环己烷萃取物中GC / MS的检出限为脂质相中的0.044 mM,确定的水生生物类群中脂质相的总摩尔浓度在0.139-168 mM的范围内,在地表水为0.26-1.34 mM的范围内系统,且饮用水<0.044 mM。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号