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Query: UMLS:C0016382 (flushing)
 6,387 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The efficacy of a new rhamnolipid biosurfactants mixture to enhance the removal of pyrene from a soil artificially contaminated was investigated. The molar solubilization ratio (MSR) and the partition coefficient between the micelles and water (log K(m)) were found to be 7.5 x 10(-3) and 5.7, respectively. From soil column studies, the pyrene removal increased linearly with the concentration of the injected biosurfactants solution above the effective critical micellar concentration (0.4 g L(-1)). Flushing with a 5.0 g L(-1) biosurfactants solution increased the pyrene concentration in the effluent by 178 times. At high biosurfactants' concentrations (2.5 and 5.0 g L(-1)), the cumulative pyrene recovery reached 70%. This pyrene remobilization takes place independently of the soil organic carbon solubilization. This study provides a combination of batch and column experiments in order to find the conditions for effective soil remediation using a new rhamnolipids mixture.
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PMID:Conditions for effective removal of pyrene from an artificially contaminated soil using Pseudomonas aeruginosa 57SJ rhamnolipids. 1590 7

This paper presents a hybrid technology of soil remediation based on the integration of biodegradation and electroosmosis. We employed soils with different texture (clay soil and loamy sand) containing a mixture of polycyclic aromatic hydrocarbons (PAH) present in creosote, and inoculation with a representative soil bacterium able to degrade fluorene, phenanthrene, fluoranthene, pyrene, anthracene, and benzo[a]pyrene. Two different modes of treatment were prospected: (i) inducing in soil the simultaneous occurrence of biodegradation and electroosmosis in the presence of a biodegradable surfactant, and (ii) treating the soils sequentially with electrokinetics and bioremediation. Losses of PAH due to simultaneous biodegradation and electroosmosis (induced by a continuous electric field) were significantly higher than in control cells that contained the surfactant but no biological activity or no current. The method was especially successful with loamy sand. For example, benzo[a]pyrene decreased its concentration by 50% after 7 d, whereas 22 and 17% of the compound had disappeared as a result of electrokinetic flushing and bioremediation alone, respectively. The use of periodical changes in polarity and current pulses increased by 16% in the removal of total PAH and in up to 30% of specific compounds, including benzo[a]pyrene. With the aim of reaching lower residual levels through bioremediation, an electrokinetic pretreatment was also evaluated as a way to mobilize the less bioaccessible fraction of PAH. Residual concentrations of total biodegradable PAH, remaining after bioremediation in soil slurries, were twofold lower in electrokinetically pretreated soils than in untreated soils. The results indicate that biodegradation and electroosmosis can be successfully integrated to promote the removal of PAH from soil.
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PMID:Integrating biodegradation and electroosmosis for the enhanced removal of polycyclic aromatic hydrocarbons from creosote-polluted soils. 1776 23

We investigated desorption of native pyrene from field-aged sediments using time-gated, laser-induced fluorescence (LIF) spectroscopy. LIF is superior to conventional analytical methods for the measurement of quickly changing dissolved pyrene because it allows observations at minute-scale resolution, has a low detection limit (approximately 1 ng/L), and minimizes sample loss and disturbance since it requires no system subsampling and chemical analysis. The efficacy of LIF was demonstrated in studies of pyrene desorption from Boston Harbor sediment segregated into different size-fractions (38-75, 75-106, and 180-250 microm diameter) and used in varying solid-to-water ratios (20, 70, and 280 mg(solid)/L). The effects of particle size and solid loading on desorption were consistent with diffusion physics. For suspension conditions between 20 and 280 mg(solids)/L, we observed desorption continuing toward an apparent plateau level over the course of weeks to months. This implies that the characteristic desorption time of pyrene from fine sediments and, by inference, other sediment-bound hydrophobic organic compounds (HOCs) of similar hydrophobicity, exceeds the typical characteristic times for pore water flushing and resuspension events. Consequently, the assumption of local sorption equilibrium in modeling efforts would be inappropriate.
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PMID:Investigating desorption of native pyrene from sediment on minute- to month-timescales by time-gated fluorescence spectroscopy. 1807 84

A back-flushing procedure using porous graphitic carbon (PGC) HPLC columns has been used successfully for the cleanup of soil samples for the determination of benzo[a]pyrene in ppb levels by an ODS-fluorescence HPLC column. The procedure was tested on nine random soil samples taken from an industrial area of the Kingdom of Bahrain. The mean percent recovery from the PGC column was 96% and the average coefficient of variation for the whole method was 5.2%.
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PMID:A selective method for the determination of benzo[a]pyrene in soil using porous graphitic carbon liquid chromatography columns. 1896 72

An innovative process that combines soil electrokinetic remediation and liquid electrochemical oxidation for the degradation of organic compounds present in a polluted soil was developed and evaluated by using benzo[a]pyrene spiked kaolin. In order to increase benzo[a]pyrene solubility during electrokinetic treatment, the addition of a co-solvent or surfactant, such as ethanol or Brij 35, as flushing solution was tested. The research carried out demonstrated the influence of the desorption agent employed on benzo[a]pyrene remediation from the kaolin matrix. Thus, if the flushing solution was ethanol at 40%, there was no presence of contaminant in either chamber. On the contrary, when a solution of surfactant Brij 35 was used, benzo[a]pyrene was transported towards the cathode chamber, where it was collected. Moreover, the extent of this recovery depends on the pH profile on the soil. When no pH control was used, around 17% of initial contaminant was detected in the cathode chamber; however, when pH control was applied, the recovery of benzo[a]pyrene could be higher than 76%, when the pH control in the anode chamber was set at 7.0. In order to obtain the total degradation of mobilised benzo[a]pyrene from the contaminated soil, the liquid collected by electrokinetic remediation was oxidised by electrochemical treatment. This oxidation was accomplished via an electrochemical cell with a working volume of 0.4 L, and graphite as electrode material. The benzo[a]pyrene was almost totally degraded in 1d, reaching a degradation of about 73% in 16 h.
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PMID:A two-stage process using electrokinetic remediation and electrochemical degradation for treating benzo[a]pyrene spiked kaolin. 1909 82

Bioturbation by the burrowing crab Helice tiensinensis was investigated to determine its impact on polycyclic aromatic hydrocarbon (PAH)-contaminated estuarine sediments. The concentrations of 16 U.S. Environmental Protection Agency (U.S. EPA) priority PAHs in sediment and pore water from a crab bed (including surface and burrow samples) and a control area, as well as in crabs, were measured. The total concentration of the 16 U.S. EPA priority PAHs in surface sediment of the crab bed (average 2,772 ng/g dry weight) was significantly higher than in the control area (1,173 ng/g dry weight). In the crab bed, the total concentration of PAHs in burrow sediment (1,239 ng/g dry weight) was lower than in surface sediment, and a similar trend was found for most of the individual PAHs, except for indeno[1,2,3-cd]pyrene, and benzo[ghi]perylene. The enhanced PAH desorption in the burrow, which could be attributed to the increase in dissolved organic matter in pore water as well as the mechanical mixing by the crab, is expected to increase PAH flux to the sea. In addition to increased flushing to the sea, incorporation of PAHs in crab biomass and metabolism of PAHs by the crab, stimulated microbial degradation, was proposed as an ignorable factor that lowered the PAH concentration in burrow sediment, because crab bioturbation increases the abundance and activity of microorganisms through several means. Log K(OW) and log K(OC) correlated well for individual PAHs in sediment in the control area, although this correlation was poor for sediments in the crab bed. The log biota-sediment accumulation factor (BSAF) of PAHs exhibited a negative relationship with log K(OW), suggesting that the bioaccumulation of sorbed PAHs was controlled primarily by their bioavailability.
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PMID:Impacts of crab bioturbation on the fate of polycyclic aromatic hydrocarbons in sediment from the Beitang estuary of Tianjin, China. 2082 66

Passive polyethylene (PE) samplers were deployed at six locations within Narragansett Bay (RI, USA) to determine sources and trends of freely dissolved and gas-phase polycyclic aromatic hydrocarbons (PAHs) from May to November 2006. Freely dissolved aqueous concentrations of PAHs were dominated by fluoranthene, pyrene, and phenanthrene, at concentrations ranging from tens to thousands of pg/L. These were also the dominant PAHs in the gas phase, at hundreds to thousands of pg/m3. All stations mostly followed the same temporal trends, with highest concentrations (up to 7300 pg/L for sum PAHs) during the second of 11 deployments, coinciding with a major rainstorm. Strong correlations of sum PAHs with river flows and wastewater treatment plant discharges highlighted the importance of rainfall in mobilizing PAHs from a combination of runoff and atmospheric washout. PAH concentrations declined through consecutive deployments III to V, which could be explained by an exponential decay due to flushing with cleaner ocean water during tides. The estimated residence time (tres) of the PAH pulse was 24 days, close to an earlier estimate of tres of 26 days for freshwater in the Bay. Air-water exchange gradients indicated net volatilization of most PAHs closest to Providence. Further south in the Bay, gradients had changed to mostly net uptake of the more volatile PAHs, but net volatilization for the less volatile PAHs. Based on characteristic PAH ratios, freely dissolved PAHs at most sites originated from the combustion of fossil fuels; only two sites were at times affected by fuel spill-derived PAHs.
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PMID:Determining air-water exchange, spatial and temporal trends of freely dissolved PAHs in an urban estuary using passive polyethylene samplers. 2135 93

Precolumn back-flushing is a matrix minimization technique in GC in which the carrier gas flow of the precolumn is reversed after the transfer of the highest boiling analyte to the analytical column. Practical details concerning this technology have rarely been published although it is widely used. This paper now focuses on the practical implementation of precolumn back-flushing for pesticide residue analysis of complex food matrices. Fitting the analytical column into the precolumn was found to be essential for comparable analyte responses with and without back-flushing. The effectiveness of the reverse column flow technique is mainly affected by the transfer time after which back-flushing starts. The transfer time was found to depend on which kind of injected matrix is used and the state of the precolumn. For the regular adaptation of the transfer time in routine analysis, a simple test was introduced in which 13-C-labeled deltamethrin and indeno[1,2,3-c,d]pyrene were added to the prepared extract. Chromatograms, LOQ and RSD of up to 99 pesticides in citrus oil and liver extracts proved a clearer identification and enhanced quantification using precolumn back-flushing compared to measurements without this technology. Furthermore, reduced system maintenance could be achieved through back-flushing.
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PMID:Application of the precolumn back-flush technology in pesticide residue analysis: a practical view. 2360 74

Although surfactant foams enhanced-remediation for PAHs-contaminated soil has been proved to be an effective method, lack of simple/economic surfactant recovery methods from the eluent solutions limit its further remediation application for organic contaminated soil. Here, we prepared a electrochemically reversible ferrocene surfactant FcCH2N+(CH3)C12H25 (Fc12), then investigated the foaming ability and foam stability of Fc12 under its reduced (active state) and oxidation (inactive state) states and explored the flushing efficiency of reduced Fc12 foam for PAHs-contaminated soil and the recovery efficiency of collected eluent solution. The results showed that the foaming ability and foam stability of reduced Fc12 are greatly higher than those of oxidized Fc12, which is indicative of a well reversibly switchable characteristic of Fc12. The contaminated soil flushing efficiencies of reduced Fc12 for phenanthrene and pyrene were 65.28% and 46.45%. The respective desorption efficiency of phenanthrene and pyrene from collected eluent solutions were calculated to be 74.94% and 72.75% by electrochemical oxidation control, which indicates that Fc12 can be well recovered by simple electrochemical control. This study provides a feasible method for the recovery of surfactants from surfactant-enhanced remediation processes by simply electrochemical control.
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PMID:Electrochemically reversible foam enhanced flushing for PAHs-contaminated soil: Stability of surfactant foam, effects of soil factors, and surfactant reversible recovery. 3269 62