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Evidence For Instantaneous Oxygen-limited Biodegradation Of Petroleum Hydrocarbon Vaporsin The Subsurface

机译:地下石油烃蒸气瞬时限氧生物降解的证据

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Petroleum hydrocarbon vapors biodegrade aerobically in the subsurface. Depth profiles of petroleum hydrocarbon vapor and oxygen concentrations from seven locations in sandy and clay soils across four states of Australia are summarized. The data are evaluated to support a simple model of biodegradation that can be used to assess hydrocarbon vapors migrating toward built environments. Multilevel samplers and probes that allow near-continuous monitoring of oxygen and total volatile organic compounds (VOCs) were used to determine concentration depth profiles and changes over time. Collation of all data across all sites showed distinct separation of oxygen from hydrocarbon vapors, and that most oxygen and hydrocarbon concentration profiles were linear or near linear with depth. The low detection limit on the oxygen probe data and because it is an in situ measurement strengthened the case that little or no overlapping of oxygen and hydrocarbon vapor concentration profiles occurred, and that indeed oxygen and hydrocarbon vapors were largely only coincident near the location where they both decreased to zero. First-order biodegradation rates determined from all depth profiles were generally lower than other published rates. With lower biodegradation rates, the overlapping of depth profiles might be expected, and yet such overlapping was not observed. A model of rapid (instantaneous) reaction of oxygen and hydrocarbon vapors compared to diffusive transport processes is shown to explain the important aspects of the 13 depth profiles. The model is simply based on the ratio of diffusion coefficients of oxygen and hydrocarbon vapors, the ratio of the maximum concentrations of oxygen and hydrocarbon vapors, the depth to the maximum hydrocarbon source concentration, and the stoichiometry coefficient. Whilst simple, the model offers the potential to incorporate aerobic biodegradation into an oxygen-limited flux-reduction approach for vapor intrusion assessments of petroleum hydrocarbon compounds.
机译:石油烃蒸气在地下被好氧生物降解。总结了澳大利亚四个州的七个地区的沙质和粘土土壤中石油烃蒸气和氧气浓度的深度分布。对数据进行评估以支持简单的生物降解模型,该模型可用于评估向建筑环境迁移的碳氢化合物蒸气。允许对氧气和总挥发性有机化合物(VOC)进行近乎连续监测的多级采样器和探针用于确定浓度深度曲线和随时间的变化。所有站点上所有数据的整理显示,氧气与碳氢化合物蒸气有明显的分离,并且大多数氧气和碳氢化合物的浓度曲线随深度呈线性或接近线性。氧气探针数据的低检测限以及由于它是原位测量,从而增强了氧气和碳氢化合物蒸气浓度分布很少或没有重叠发生的情况,并且实际上氧气和碳氢化合物蒸气仅在重合的位置附近重合的情况两者都降低到零。从所有深度剖面确定的一级生物降解率通常低于其他已公布的速率。随着较低的生物降解率,深度剖面可能会重叠,但是没有观察到这种重叠。与扩散传输过程相比,氧气和碳氢化合物蒸气的快速(瞬时)反应模型显示出可以解释13个深度剖面的重要方面。该模型仅基于氧气和碳氢化合物蒸气的扩散系数之比,氧气和碳氢化合物蒸气之最大浓度之比,深度与最大碳氢化合物源浓度之比以及化学计量系数。虽然简单,但该模型提供了将有氧生物降解方法纳入氧气受限的通量减少方法中的潜力,从而可用于评估石油烃化合物的蒸汽侵入。

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