Purpose
In order to provide highly effective yet relatively inexpensive strategies for the remediation of recalcitrant organic contaminants, research has focused on in situ treatment technologies. Recent investigation has shown that coupling two common treatments—in situ chemical oxidation (ISCO) and in situ bioremediation—is not only feasible but in many cases provides more efficient and extensive cleanup of contaminated subsurfaces. However, the combination of aggressive chemical oxidants with delicate microbial activity requires a thorough understanding of the impact of each step on soil geochemistry, biota, and contaminant dynamics. In an attempt to optimize coupled chemical and biological remediation, investigations have focused on elucidating parameters that are necessary to successful treatment. In the case of ISCO, the impacts of chemical oxidant type and quantity on bacterial populations and contaminant biodegradability have been considered. Similarly, biostimulation, that is, the adjustment of redox conditions and amendment with electron donors, acceptors, and nutrients, and bioaugmentation have been used to expedite the regeneration of biodegradation following oxidation. The purpose of this review is to integrate recent results on coupled ISCO and bioremediation with the goal of identifying parameters necessary to an optimized biphasic treatment and areas that require additional focus. 相似文献Purpose
The consequences of permanent inundation and storage of flood plain soils and aquatic sediments on metal mobility were studied. The main goal was to quantify kinetic mobilisation processes in order to pinpoint the conditions that pose emission risks to groundwater and surface waters. 相似文献Purpose
Sediments can function as secondary source for water pollution of aerobically biodegradable non-halogenated organic compounds, which are persistent in anaerobic sediments. The mass transfer of compounds from sediment to bulk water depends on hydraulic conditions. In this study, desorption, mass transfer and biodegradation are investigated under settled and resuspended sediment conditions for branched nonylphenol (NP), which was used as model compound for aerobically biodegradable and anaerobic persistent compounds. 相似文献Stripping contaminants from sediments with granular activated carbon (GAC) is a promising remediation technique in which the effectiveness depends on the rate of contaminant extraction from the sediment by the GAC. The purpose of the present study was to investigate the effect of mixing intensity on the short-term extraction rate of polycyclic aromatic hydrocarbons (PAHs) from contaminated sediment.
Materials and methodsPAH desorption from sediment at a wide range of rotational speeds (min?1; rotations per minute (rpm)) was monitored by uptake in Tenax polymeric resins using a completely mixed batch reactor. Desorption data were interpreted using a radial diffusion model. Desorption parameters obtained with the radial diffusion model were correlated with particle size measurements and interpreted mechanistically.
Results and discussionFast desorption rate constants, D e /r 2, with D e the effective diffusion coefficient and r the particle radius, ranged from 3.7 × 10?3 to 1.1 × 10?1 day?1 (PHE) and 6 × 10?6 to 1.9 × 10?4 day?1 (CHR), respectively, and increased with the intensity of mixing. The D e /r 2 values would correspond to D e ranges of 1.8 × 10?14–1.2 × 10?16 m2 × day?1 and 1.8 × 10?12–3.7 × 10?15 m2 × day?1, assuming fast desorption from the measured smallest particle size (9 μm) classes at 200 and 600 rpm, respectively.
ConclusionsDesorption of PAHs was significantly accelerated by a reduction of particle aggregate size caused by shear forces that were induced by mixing. The effective intra-particle diffusion coefficients, D e , were larger at higher mixing rates.
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