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Mobilization of Soil-Bound Residue of Organochlorine Pesticides and Polycyclic Aromatic Hydrocaitons in an in vitro Gastrointestinal Model

机译:在体外胃肠道模型中动员土壤中有机氯农药和多环芳烃的残留

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摘要

A previous study on mobilization of organochlorine pesticides (OCPs) in contaminated soils from the field revealed that the total amount of OCPs measured in digestive fluid and chyme of an in vitro gastrointestinal model was higher than the quantity directly extracted using a solvent extraction without digestion, providing a clue that the bound residue of OCPs might be mobilized. This hypothesis was tested in this study for both OCPs and polycyclic aromatic hydrocarbons (PAHs). Three contaminated surface soil samples with different organic carbon (OC) contents were collected from the field, and extracted with a solvent with and without digestion in an in vitro gastrointestinal model. It was found that bound residues of OCPs and PAHs were mobilized to a certain extent during digestion. The ratios of the mobilized bound residues over the total quantities extracted after digestion (R_b) varied from 0 to 0.96 for individual compounds. The fit was positively correlated with OC content Among the five constitutes of digestive juice, bile salt was the only one that served to mobilize the bound residues and the extractability of bile salt was constant over a concentration range from 2 to 20 mg/mL The mobilization process followed typical first-order kinetics. The calculated rate constants suggest that mobilization was fast and 90% of extracted bound residues of OCPs and PAHs were mobilized within 2.4 and 4.8 h, respectively.
机译:先前关于在野外污染土壤中动员有机氯农药(OCP)的研究表明,体外胃肠道模型在消化液和食糜中测得的OCP总量要比不经消化的溶剂萃取直接提取的量高,提供了可能动员了OCP结合残基的线索。该假设在本研究中针对OCP和多环芳烃(PAH)进行了测试。从田间收集了三个具有不同有机碳(OC)含量的受污染的表层土壤样品,并在体外胃肠道模型中在有和没有消化的情况下用溶剂萃取。发现在消化过程中OCP和PAH的结合残基在一定程度上被动员。对于单个化合物,动员的结合残基在消化后提取的总量(R_b)中的比率在0到0.96之间变化。拟合度与OC含量呈正相关。在消化液的五种成分中,胆汁盐是唯一一种能动员结合的残留物的物质,胆汁盐的可萃取性在2至20 mg / mL的浓度范围内是恒定的。过程遵循典型的一阶动力学。计算出的速率常数表明,动员速度很快,OCP和PAH的90%提取的结合残基分别在2.4和4.8小时内动员。

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  • 来源
    《Environmental Science & Technology》 |2011年第3期|p.1127-1132|共6页
  • 作者单位

    Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

    rnLaboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, Oana;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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