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Solid-Phase-Microextraction Measurement of 62 Polychlorinated Biphenyl Congeners in Milliliter Sediment Pore Water Samples and Determination of K_(DOC) Values

机译:毫升沉积物孔隙水样品中62种多氯联苯同源物的固相微萃取测定和K_(DOC)值的确定

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Determining dissolved concentrations of polychlorinated biphenyls (PCBs) in sediment pore (interstitial) water with conventional solvent extraction methods is problematic because obtaining large (liter) quantities of pore water, separating it from the sediment, and removing the influence of colloids can be very difficult. However, solid-phase-microextraction (SPME) can achieve similar detection limits using milliliter water samples as achieved with organic solvent extraction requiring a liter of pore water. Five different SPME sorbents were evaluated for their ability to yield the best detection limits for di- to octachlorobiphenyl congeners, both with GC/ECD and with GC/MS (both positive ion EI and negative ion CI). SPME using the 7 (mu)m PDMS fiber with GC/MS (positive ion EI) yielded the best combination of signal-to-noise and selectivity using a 30 min extraction, although ECD was also suitable. Pore water was obtained by centrifuging wet sediment followed by flocculation to remove colloids. Quantitative calibration was simplified by adding dichloro-to hexachlorobiphenyl internal standards chosen to be compatible with either ECD or MS detection. Calibration curves and relative response factors (including the SPME and GC steps) were determined for all 62 PCB congeners that are present in above-trace quantities in commercial Aroclors. Calibrations were linear (r~(2) typically > 0.995) from low pg/mL to ng/mL concentrations, with near zero intercepts. Detection limits for all individual PCB congeners ranged from <1 to 3 pg/mL using 1.5 mL water samples. Dissolved organic matter (DOM) had no measurable effect on dichloro- and trichlorobiphenyls, but did contain about 10 to 25percent of the tetrachlorobiphenyls and up to 60percent of the hexachlorobiphenyl congeners. Log DOC/water partitioning coefficients (log K_(DOC)) ranged from 3.6 to 4.6 for 2,3,5,6-tetra-chlorobiphenyl and from 4.2 to 5.5 for 3,3',4,4',5,5'-hexachlorobiphenyl.
机译:用传统的溶剂萃取方法确定沉积物孔隙(间隙)水中多氯联苯(PCBs)的溶解浓度是有问题的,因为要获得大量(升)孔隙水,将其与沉积物分离,并消除胶体的影响可能非常困难。 。但是,固相微萃取(SPME)可以使用毫升水样品达到与需要一升孔隙水的有机溶剂萃取所达到的相似检测限。使用GC / ECD和GC / MS(正离子EI和负离子CI)对五种不同的SPME吸附剂对二至八氯联苯同类物的最佳检测限进行了评估。使用7 µm PDMS纤维和GC / MS(正离子EI)的SPME使用30分钟萃取可以得到信噪比和选择性的最佳组合,尽管ECD也适用。通过离心湿的沉淀物,然后絮凝去除胶体,获得孔隙水。通过将二氯-六氯联苯内标添加为与ECD或MS检测兼容的方法,简化了定量校准。确定了所有62种PCB同类品的校准曲线和相对响应因子(包括SPME和GC步骤),这些商品均以商品名Aroclors中的痕量以上存在。从低pg / mL到ng / mL的浓度,校准是线性的(r〜(2)通常> 0.995),截距接近零。使用1.5 mL水样品,所有单个PCB同系物的检出限范围为<1 pg / mL至3 pg / mL。溶解的有机物(DOM)对二氯联苯和三氯联苯没有可测量的影响,但确实含有约10%至25%的四氯联苯和高达60%的六氯联苯同类物。 Log DOC /水分配系数(log K_(DOC))对于2,3,5,6-四氯联苯为3.6至4.6,对于3,3',4,4',5,5'为4.2至5.5 -六氯联苯。

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