首页> 外文期刊>Journal of Environmental Science and Health, Part B: Pesticides, Food Contaminants, and Agricultural Wastes >Determination of octanol-air partition coefficients and supercooled liquid vapor pressures of organochlorine pesticides
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Determination of octanol-air partition coefficients and supercooled liquid vapor pressures of organochlorine pesticides

机译:有机氯农药辛醇-空气分配系数和过冷液体蒸气压的测定

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Octanol-air partition coefficients (KOA) and supercooled liquid vapor pressures (PL) of nine organochlorine pesticides (OCPs) including p,p′-DDE, p,p′-DDD, o,p′-DDT, o,p′-DDE, o,p′-DDD, α-HCH, β-HCH, γ-HCH, δ-HCH were determined as functions of temperature using a gas chromatographic retention time method. Among them, the KOA of o,p′-DDE and o,p′-DDD and the PL of o,p′-DDE, o,p′-DDD, β-HCH and δ-HCH were determined for the first time. The determined KOA and PL values of investigated compounds at 25°C ranged from 3.14 × 107 (α-HCH) to 3.76×109 (p,p′-DDD), and 8.95×10− 4 Pa (p,p′-DDD) to 1.08×10− 1 Pa (α-HCH), respectively. The KOA and PL data were compared with published data. The KOA values of o,p′-DDT at 25°C were 3.23×109, higher than o,p′-DDE (1.02×109) and o,p′-DDD (2.01×109), indicating o,p′-DDT were more preferred to partition in soil compared with the metabolites. The KOA values were lower and PL values were higher for o,p′-DDE and o,p′-DDD, compared with their p,p′-isomeric counterparts, leading to a potential difference in behavior and fate of these isomers. The discrepancies among chemicals are obvious, which reflected in the increasing KOA and decreasing PL values in order of α-HCH, γ-HCH, β-HCH, δ-HCH, o,p′-DDE, p,p′-DDE, o,p′-DDD, o,p′-DDT, p,p′-DDD. For each compound, the LogKOA decreased linearly with reciprocal absolute temperature, while LogPL had a significant positive correlation with the inverse absolute temperature. The present study suggested that the method of gas chromatographic retention time was appropriate to measure the KOA and PL of a number of OCPs.
机译:九种有机氯农药(OCP)的辛醇-空气分配系数(K OA )和过冷液体蒸气压(P L ),包括p,p€-DDE,p,确定为pâ-DDD,o,pâ-DDT,o,pâ-DDE,o,pâ-DDD,α-HCH,β-HCH,γ-HCH,β-HCH使用气相色谱保留时间方法确定温度的函数。其中,o,pâ-DDE和o,pâ-DDD的K OA 和o,pâ-DDE,o的P L ,p-DDD,β-六氯环己烷和β-六氯环己烷被首次确定。确定的K OA 和P L 值在25°C的调查的化合物范围从3.14×10 7 (α-HCH) 3.76×10 9 (p,pâ€-DDD)和8.95×10 ∠4 Pa(p,p€-DDD)至1.08 Pa 10 â1 Pa(α-HCH)。将K OA 和P L 数据与已发布数据进行比较。 o,p€-DDT在25°C时的K OA 值为3.23×10 9 ,高于o,p€-DDE(1.02× 10 9 )和o,pâ-DDD(2.01×10 9 ),表明与土壤相比,o,pâ-DDT更适合在土壤中分配代谢产物。与它们的p,p相比,o,p€-DDE和o,p€-DDD的K OA 值较低,而P L 值较高。 ²异构体,导致这些异构体的行为和命运存在潜在差异。化学品之间的差异是显而易见的,这反映在K OA 的增加和P L 的值按α-HCH,γ-HCH,β-HCH,α的顺序减少‘-HCH,o,p” -DDE,p,p” -DDE,o,p” -DDD,o,p” -DDT,p,p” -DDD。对于每种化合物,LogK OA 随绝对绝对温度线性下降,而LogP L 与绝对绝对温度呈显着正相关。本研究表明,气相色谱保留时间的方法适用于测量多种OCP的K OA 和P L

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