Washing technologies are currently applied for the remediation of contaminated soils. The efficiency of biosurfactants produced by Pseudomonas aeruginosa strains to mobilize some hydrocarbons sorbed on soils has already been demonstrated. However, few studies have been made to define optimal procedures for the injection of these rhamnolipids in soil. This study examines (1) the efficiency of the biosurfactants produced by P. aeruginosa UG2 to mobilize pyrene from a contaminated sandy loam as compared to that of sodium dodecyl sulfate (SDS); (2) the injection procedures (surfactant concentration, pore water velocity, continuous or interrupted flow) that might affect the efficiency of pyrene mobilization using UG2 biosurfactants; and (3) the co-transport of UG2 biosurfactants and pyrene. The UG2 biosurfactants were more efficient for pyrene mobilization than SDS and had much less impact on soil. The mobilization of pyrene was approximately proportional to the mass of UG2 biosurfactants injected for both the 0.25% and the 0.50% (w/v) concentrations used. Pyrene mobilization was not greatly dependent on either the pore water velocity—about 5.9 and 10.2 inch/h (15 and 26 cm/h)—or the duration of flow interruption (5 or 15 h), suggesting that mobilization was not rate limited under these conditions. The rhamnolipids appeared to be weakly retained in the soil. Based on the experimental results, it would be advantageous to use a high UG2 biosurfactant concentration, a high pore water velocity, and possibly a flow interruption of more than 15 h in order to reduce the injected volume and the duration of the treatment required. The 0.25% UG2 biosurfactant concentration greatly enhanced pyrene transport and could facilitate contaminant recovery. 相似文献
The aim of this review is to examine the present knowledge about water structure close to an interface or confined in porous spaces. First, the structure of liquid water is briefly described. Though its understanding remains incomplete, it appears that it is largely dominated by the hydrogen bond network and its dynamical evolution. The presence of any ‘foreign’ substance in water perturbs such a structure by changing at least locally the hydrogen bond network. For this reason, the presence of a solid interface significantly modifies the structure of the first adsorbed layers. Whatever the support, it is now clearly evidenced that structural perturbations are limited to distances lower than 10–15 Å from the interface. The nature, energetic heterogeneity and hydrophilicility/hydrophobicity of the solid surface influence the arrangement of water molecules. This surface organisation must definitely be considered when studying adsorption phenomena at the solid–aqueous solution interface. The relevance of such problems to geosciences is illustrated by a few situations in which water structure plays a prominent role. To cite this article: L.J. Michot et al., C. R. Geoscience 334 (2002) 611–631.相似文献
This article demonstrates the operation of a simple optimal location‐allocation technique for solving the problem of locating one or several community recycling center(s) within a residential area. The article attempts to measure both transportation and externality costs in comparable units, and to incorporate them into the model. A sensitivity analysis of the results at the level of the nuisance provides further insight into the operation of the model and the relative importance of the quantification of pollution in applied location‐allocation problems. 相似文献
Ocean Dynamics - A dense network of instruments has been deployed within harbors along the Mediterranean coast, in the Toulon Metropole area, between the Hyères islands and the Sanary Bay in... 相似文献
The composition of crude oil in a surficial aquifer was determined in two locations at the Bemidji, MN, spill site. The abundances of 71 individual hydrocarbons varied within 16 locations sampled. Little depletion of these hydrocarbons (relative to the pipeline oil) occurred in the first 10 years after the spill, whereas losses of 25% to 85% of the total measured hydrocarbons occurred after 30 years. The C6‐30n‐alkanes, toluene, and o‐xylene were the most depleted hydrocarbons. Some hydrocarbons, such as the n‐C10–24 cyclohexanes, tri‐ and tetra‐ methylbenzenes, acyclic isoprenoids, and naphthalenes were the least depleted. Benzene was detected at every sampling location 30 years after the spill. Degradation of the oil led to increases in the percent organic carbon and in the δ13C of the oil. Another method of determining hydrocarbon loss was by normalizing the total measured hydrocarbon concentrations to that of the most conservative analytes. This method indicated that the total measured hydrocarbons were depleted by 47% to 77% and loss of the oil mass over 30 years was 18% to 31%. Differences in hydrocarbon depletion were related to the depth of the oil in the aquifer, local topography, amount of recharge reaching the oil, availability of electron acceptors, and the presence of less permeable soils above the oil. The results from this study indicate that once crude oil has been in the subsurface for a number of years there is no longer a “starting oil concentration” that can be used to understand processes that affect its fate and the transport of hydrocarbons in groundwater. 相似文献
The present paper presents the results of a technique based on Vertical Seismic Profiling (VSP) to quantify the offset of a fault in a context where seismic reflection profiles do not image any reflectors. The case study is located in Greece, in the Aigion area, on the south border of the Corinth Gulf. The Aigion fault, oriented East–West, and dipping at 60°N, has been intersected by the scientific well Aig-10 at 760 m in depth, but some uncertainty remained concerning its exact offset since the depth of the pre-rift sequence is open to debate due to the lack of subsurface data. The pre-rift consists of a Mesozoic low-porosity series (carbonates and radiolarite), while the syn-rift consists of poorly compacted conglomerates and turbidites.
Seismic diffractions on fault edges are expected to be present along the fault surface. We find that a few diffracted events are effectively recorded in P and S wave mode by the 4 components of the VSP survey, and critically refracted arrivals along the Aigion fault plane. These singular events have been used in order to refine the fault geometry and to determine its throw. Additionally, results from a 2D finite difference elastic seismic model of a single fault step geometry have been closely examined in order to illustrate the generation of the singular seismic events observed on the field data, such as P-wave and S-wave refracted and diffracted events, and support their interpretation with higher confidence. As a result, the seismic arrival patterns from full waveform seismic modelling confirm the characterisation of the main fault geometry (mainly its throw: about 200 m) in the well vicinity derived from the actual analysis of the 4 Component Aigion VSP data. 相似文献
The Khushaym Matruk site in central Jordan may represent a natural analogue depicting the interaction of alkaline solutions with a clayey sedimentary formation or with clay-rich confining barriers at the interface with concrete structures in waste disposal sites. In this locality, past spontaneous combustion of organic matter in a clayey biomicritic formation produced a ca. 60 m-thick layer of cement-marble containing some of the high-temperature phases usually found in industrial cements (e.g., spurrite, brucite, and Ca-aluminate). A vertical cross-section of the underlying sediments was used in order to study the interaction between cement-marbles and neighbouring clayey limestones under weathering conditions. A thermodynamic approach of the alteration parageneses (calcite–jennite–afwillite–brucite and CSH phases) in the cement-marbles constrains the interacting solutions to have had pH-values between 10.5 and 12. Over 3 m, the sediments located beneath the metamorphic unit were compacted and underwent carbonation. They display large C and O isotopic variations with respect to “pristine” sediments from the bottom of the section. Low δ13C-values down to −31.4‰/PDB show the contribution of CO2 derived from the oxidization of organic matter and from the atmosphere to the intense carbonation process affecting that particular sedimentary level. The size of the C isotopic anomalies, their geometrical extent and their coincidence with the variations of other markers like the Zn content, the structure of organic matter, the mineralogical composition, all argue that the carbonation process was induced by the percolation of high pH solutions which derived from the alteration of cement-marbles. The temperature of the carbonation process remains conjectural and some post-formation O isotopic reequilibration likely affected the newly-formed carbonate. Carbonation induced a considerable porosity reduction, both in fractures and matrixes. The Khushaym Matruk site may have some bearing to the early life of a repository site, when water saturation of the geological formations hosting the concrete structures is incomplete, enabling simultaneous diffusion of alkaline waters and gaseous CO2 in the near field. 相似文献