In situ Biorestoration of an Oil Contaminated Subsoil

1988 ◽  
Vol 20 (3) ◽  
pp. 255-256 ◽  
Author(s):  
R. van den Berg ◽  
J H. A. M. Verheul ◽  
D. H. Eikelboom

The feasibility of in-situ biorestoration of contaminated subsoils is being investigated by RIVM in co-operation with TNO. This project is aimed at optimizing the treatment of deeper layers of contaminated soil by enhancing microbial activity. The project consists of a literature study, research at laboratory-scale, detailed research of the selected experimental site and the actual clean-up of the contaminated site. In the literature study it was concluded that in-situ biological treatment offers reasonable prospects, concerning the technical aspects and the final results, but there were still questions about the efficiency of the clean-up of the soil itself. The selected site is a gasoline station, where the soil has been contaminated with gasoline, caused by a leaking tank. At least 30 m of normal gasoline have leaked and about 600 m3 of soil have been contaminated. Several monitoring wells have been placed to get an impression of the quantity and composition of the contamination. The soil consists of medium fine sand, without organic material and contains some clay-loam layers. The groundwater level is at about 2.5 m below the surface. Concentrations of the oil components in the soil(mainly between 1,000 and 5,000 mg/kg) as well as in the groundwater exceed the Dutch reference values which demand treatment of the site. In leaching experiments it was found that only very small quantities of the gasoline can be leached from the soil. Clean-up by percolation only would take at least 4 years. The leached quantity increased with the percolation rate, but was nearly independent of the gasoline concentration. The mobility could not be promoted by the addition of detergents. Numerous laboratory biodegradation experiments have been carried out in order to determine the degradation capacity of the contaminated soil, and to determine to what extent this biodegradation could be stimulated. The conlusions of these experiments are:In the soil there is low microbial activity and also the rate of degradation of the oil is low and constant in time. From mass balance studies it was determined that the degradation rate is determined by the availability of the oil components, which is a function of the dissoiution rate into the water and the volatilization. Availability turns out to be one of the determining aspects for this type of restoration technique.The degradation activity is most enhanced by the addition of seeding material from a landfarm, but is practically not feasible because of the limited mobility of microorganisms in soil.The presence of water and buffering at a neutral pH contribute to an optimal biodegradation rate.Some N and P additions are necessary. However, the C-N-P ratio had a very small influence on the degradation. A C-N-P ratio of 100-10-10 is recommended.As alternative oxygen source, hydrogen peroxide seems suitable, but the use of high concentrations of nitrate led to a decreased degradation.Detergents applied to increase the availability of the oil components did not stimulate the degradation. The degradation rate under stimulated conditions varied between 5 and 40 (mean 10) mg C/kg/day in comparison with an autonomous degradation rate of 3-4 mg C/kg/day. A stimulated clean-up duration of 1.5 years is expected. Column experiments are in progress now and are used to confirm the findings of the laboratory tests. They should also give answers about oxygen limitation and alternative oxygen sources. First examples of the hydrological set-up (infiltration by drains and withdrawal by wells, dimensioned by the desired degradation rate) confirm the feasibility of this project. It is expected that the actual clean-up operation will start in the fall of this year. In-situ treatment offers a very good alternative with advantages over excavation combined with various treatment techniques.

Water ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 2364
Author(s):  
Martin V. Maier ◽  
Yvonne Wolter ◽  
Daniel Zentler ◽  
Christian Scholz ◽  
Charlotte N. Stirn ◽  
...  

Arsenic (As) contamination of groundwater is commonly remediated by pump and treat. However, this technique is difficult to apply or maintain efficiently because the mobility of arsenic varies depending on the geochemical aquifer conditions. Arsenic interacting with the sediment can cause strong retardation, which is counteracted by ions competing for sedimentary sorption sites like silica, bicarbonate and phosphate. Phosphate competes most effectively with arsenic for sorption sites due to its chemical similarity. To accelerate an ongoing but ineffective pump and treat remediation, we examined the competitive effect of increasing phosphate doses on contaminated aquifer material of different depths and thus under distinct geochemical conditions. In the columns with phosphate addition, significant amounts of arsenic were released rapidly under oxic and anoxic conditions. In all tests, the grade of leaching was higher under anoxic conditions than under oxic conditions. As(III) was the dominant species, in particular during the first release peaks and the anoxic tests. Higher amounts of phosphate did not trigger the arsenic release further and led to a shift of arsenic species. We suggest that the competitive surface complexation is the major process of arsenic release especially when higher amounts of phosphate are used. Commonly arsenic release is described at iron reducing conditions. In contrast, we observed that a change in prevailing redox potential towards manganese reducing conditions in the oxic tests and iron reducing conditions in the anoxic column took place later and thus independently of arsenic release. The reduction of As(V) to As(III) under both redox conditions is presumed to be an effect of microbial detoxification. A loss of sulphate in all columns with phosphate indicates an increased microbial activity, which might play a significant role in the process of arsenic release. Preliminary tests with sediment material from a contaminated site showed that phosphate additions did not change the pH value significantly. Therefore, a release of other metals is not likely. Our results indicate that in-situ application of phosphate amendments to arsenic-contaminated sites could accelerate and enhance arsenic mobility to improve the efficiency of pump and treat remediation without negative side effects. The novelty of this approach is the use of only small amounts of phosphate in order to stimulate microbial activity in addition to surface complexation. Therefore, this method might become an innovative and cost-effective remediation for arsenic contaminated sites.


2017 ◽  
pp. 1001-1008
Author(s):  
Ana Paola Vilches ◽  
Dan Bylund ◽  
Anders Jonsson

The contamination of soils by petroleum hydrocarbons, such as diesel fuel, has since many years been a serious environmental problem. Treatment of contaminated areas is a concern for governments and environmental authorities in several countries and efforts have been done with the purpose to eliminate this problem. Different methods have been tested and today the most common technique involves the excavation and transportation of contaminated soil to special treatment facilities. In earlier studies we have demonstrated the effect of adding organic amendments, such as fermented whey, on the biodegradation of n-alkanes in diesel contaminated soil. Non-fermented sweet whey also proved significantly to enhance the biodegradation of an aromatic substance (phenanthrene) in contaminated soil. The current paper presents the results of an in-situ field test at a former gas station in the north of Sweden. In parallel to the field study, biodegradation profiles were monitored under controlled laboratory conditions by taking soil samples from the contaminated site and spike them with diesel fuel. The experiments were carried out by adding whey and mineral nutrients (NPK) to the test area and to the laboratory samples, and monitor the degradation of hydrocarbons by gas chromatographic analysis of extracted soil samples. Significant effects on the degradation rates were achieved in the laboratory tests. For the in-situ test, however, no such positive effects could be registered.


Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 228
Author(s):  
Rute Cesário ◽  
Nelson J. O’Driscoll ◽  
Sara Justino ◽  
Claire E. Wilson ◽  
Carlos E. Monteiro ◽  
...  

In situ air concentrations of gaseous elemental mercury (Hg(0)) and vegetation–atmosphere fluxes were quantified in both high (Cala Norte, CN) and low-to-moderate (Alcochete, ALC) Hg-contaminated saltmarsh areas of the Tagus estuary colonized by plant species Halimione portulacoides (Hp) and Sarcocornia fruticosa (Sf). Atmospheric Hg(0) ranged between 1.08–18.15 ng m−3 in CN and 1.18–3.53 ng m−3 in ALC. In CN, most of the high Hg(0) levels occurred during nighttime, while the opposite was observed at ALC, suggesting that photoreduction was not driving the air Hg(0) concentrations at the contaminated site. Vegetation–air Hg(0) fluxes were low in ALC and ranged from −0.76 to 1.52 ng m−2 (leaf area) h−1 for Hp and from −0.40 to 1.28 ng m−2 (leaf area) h−1 for Sf. In CN, higher Hg fluxes were observed for both plants, ranging from −9.90 to 15.45 ng m−2 (leaf area) h−1 for Hp and from −8.93 to 12.58 ng m−2 (leaf area) h−1 for Sf. Mercury flux results at CN were considered less reliable due to large and fast variations in the ambient air concentrations of Hg(0), which may have been influenced by emissions from the nearby chlor-alkali plant, or historical contamination. Improved experimental setup, the influence of high local Hg concentrations and the seasonal activity of the plants must be considered when assessing vegetation–air Hg(0) fluxes in Hg-contaminated areas.


2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Masahiko Katoh ◽  
Wataru Kitahara ◽  
Takeshi Sato

This study aimed to identify how the ratio of inorganic-to-organic components in animal manure compost (AMC) affected both lead immobilization and microbial activity in lead-contaminated soil. When AMC containing 50% or more inorganic fraction with high phosphorous content was applied to contaminated soil, the amounts of water-soluble lead in it were suppressed by over 88% from the values in the soil without compost. The residual fraction under sequential extraction increased with the inorganic fraction in the AMC; however, in those AMCs, the levels of microbial enzyme activity were the same or less than those in the control soil. The application of AMC containing 25% inorganic fraction could alter the lead phases to be more insoluble while improving microbial enzyme activities; however, no suppression of the level of water-soluble lead existed during the first 30 days. These results indicate that compost containing an inorganic component of 50% or more with high phosphorus content is suitable for immobilizing lead; however, in the case where low precipitation is expected for a month, AMC containing 25% inorganic component could be used to both immobilize lead and restore microbial activity.


2014 ◽  
Vol 14 (19) ◽  
pp. 10761-10772 ◽  
Author(s):  
S. S. Steimer ◽  
M. Lampimäki ◽  
E. Coz ◽  
G. Grzinic ◽  
M. Ammann

Abstract. Atmospheric soluble organic aerosol material can become solid or semi-solid. Due to increasing viscosity and decreasing diffusivity, this can impact important processes such as gas uptake and reactivity within aerosols containing such substances. This work explores the dependence of shikimic acid ozonolysis on humidity and thereby viscosity. Shikimic acid, a proxy for oxygenated reactive organic material, reacts with O3 in a Criegee-type reaction. We used an environmental microreactor embedded in a scanning transmission X-ray microscope (STXM) to probe this oxidation process. This technique facilitates in situ measurements with single micron-sized particles and allows to obtain near-edge X-ray absorption fine structure (NEXAFS) spectra with high spatial resolution. Thus, the chemical evolution of the interior of the particles can be followed under reaction conditions. The experiments show that the overall degradation rate of shikimic acid is depending on the relative humidity in a way that is controlled by the decreasing diffusivity of ozone with decreasing humidity. This decreasing diffusivity is most likely linked to the increasing viscosity of the shikimic acid–water mixture. The degradation rate was also depending on particle size, most congruent with a reacto-diffusion limited kinetic case where the reaction progresses only in a shallow layer within the bulk. No gradient in the shikimic acid concentration was observed within the bulk material at any humidity indicating that the diffusivity of shikimic acid is still high enough to allow its equilibration throughout the particles on the timescale of hours at higher humidity and that the thickness of the oxidized layer under dry conditions, where the particles are solid, is beyond the resolution of STXM.


2021 ◽  
Vol 22 ◽  
pp. 101388
Author(s):  
Shichao Liu ◽  
Zhonglei Xie ◽  
Yintao Zhu ◽  
Yanmiao Zhu ◽  
Yan Jiang ◽  
...  

Pedosphere ◽  
2007 ◽  
Vol 17 (3) ◽  
pp. 383-388 ◽  
Author(s):  
Ye YANG ◽  
Ying-Xu CHEN ◽  
Guang-Ming TIAN ◽  
Zi-Jian ZHANG

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