Littérature scientifique sur le sujet « Biobarriera »
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Articles de revues sur le sujet "Biobarriera"
Harris, J. Roger, Alex X. Niemiera, Robert D. Wright et Charles H. Parkerson. « Chemically Controlling Root Escape in Pot-in-pot Production of River Birch and Yoshino Cherry ». HortTechnology 6, no 1 (janvier 1996) : 30–34. http://dx.doi.org/10.21273/horttech.6.1.30.
Texte intégralFuhrmann, Gregor, Brigitta Loretz, Nicole Schneider-Daum et Claus-Michael Lehr. « Biobarriers 2018 ». European Journal of Pharmaceutics and Biopharmaceutics 158 (janvier 2021) : 52. http://dx.doi.org/10.1016/j.ejpb.2020.10.014.
Texte intégralLennox, John, et Jeffrey Ashe. « Biofilms as Biobarriers ». American Biology Teacher 71, no 1 (1 janvier 2009) : 20–26. http://dx.doi.org/10.2307/27669358.
Texte intégralGilman, Edward. « Root Barriers affect Root Distribution ». Arboriculture & ; Urban Forestry 22, no 3 (1 mai 1996) : 151–54. http://dx.doi.org/10.48044/jauf.1996.022.
Texte intégralRuter, John M. « 354 REDUCING ROOTING-OUT PROBLEMS IN POT-IN-POT PRODUCTION SYSTEMS ». HortScience 29, no 5 (mai 1994) : 481d—481. http://dx.doi.org/10.21273/hortsci.29.5.481d.
Texte intégralJacobs, Karel, Bill Rao, Brian Jeffers et Donna Danielson. « The Effect of Biobarrier® on Mycorrhizae in Oak and Sweetgum ». Arboriculture & ; Urban Forestry 26, no 2 (1 mars 2000) : 92–96. http://dx.doi.org/10.48044/jauf.2000.011.
Texte intégralRuter, John M. « Evaluation of Control Strategies for Reducing Rooting-Out Problems in Pot-In-Pot Production Systems ». Journal of Environmental Horticulture 12, no 1 (1 mars 1994) : 51–54. http://dx.doi.org/10.24266/0738-2898-12.1.51.
Texte intégralCareghini, A., S. Saponaro et E. Sezenna. « Biobarriers for groundwater treatment : a review ». Water Science and Technology 67, no 3 (1 février 2013) : 453–68. http://dx.doi.org/10.2166/wst.2012.599.
Texte intégralWilson, R. D., W. C. Yip et C. N. Naas. « Assessing performance of a permeable biobarrier ». Proceedings of the Institution of Civil Engineers - Water Management 161, no 6 (décembre 2008) : 375–79. http://dx.doi.org/10.1680/wama.2008.161.6.375.
Texte intégralTiehm, A., A. Müller, S. Alt, H. Jacob, H. Schad et C. Weingran. « Development of a groundwater biobarrier for the removal of polycyclic aromatic hydrocarbons, BTEX, and heterocyclic hydrocarbons ». Water Science and Technology 58, no 7 (1 octobre 2008) : 1349–55. http://dx.doi.org/10.2166/wst.2008.730.
Texte intégralThèses sur le sujet "Biobarriera"
DAGHIO, MATTEO. « Degradazione degli idrocarburi con accettori solidi di elettroni. Caratterizzazione delle comunità microbiche e potenziali applicazioni ». Doctoral thesis, Università degli Studi di Milano-Bicocca, 2015. http://hdl.handle.net/10281/72473.
Texte intégralMORICI, Claudia. « Tecniche di biorisanamento delle acque di falda contaminate da nitrati ». Doctoral thesis, Università degli Studi di Palermo, 2014. http://hdl.handle.net/10447/91254.
Texte intégralSomayajula, Sreerama Murthy Kasi. « In Situ Groundwater Remediation using Enricher Reactor-Permeable Reactive Biobarrier ». Diss., North Dakota State University, 2012. https://hdl.handle.net/10365/26648.
Texte intégralMann, VANESSA. « LABORATORY STUDIES OF BIOBARRIER TECHNOLOGY IN FRACTURED ROCK ». Thesis, 2012. http://hdl.handle.net/1974/7649.
Texte intégralThesis (Ph.D, Civil Engineering) -- Queen's University, 2012-11-22 11:23:24.065
Liu, Chao-Wen, et 劉詔文. « Removal of TCE and VC in Groundwater by a Biobarrier ». Thesis, 2004. http://ndltd.ncl.edu.tw/handle/58874019967091606047.
Texte intégral國立中央大學
環境工程研究所
92
The biodegradation and removal of trichloroethylene (TCE) and vinyl chloride (VC) in groundwater under aerobic condition by indigenous soil cells and toluene-degrading cell (Pseudomonas putida F1) were investigated in this study. A series of batch experiments using toluene as co-substrate to induce toluene dioxygenase (TDO) for co-metabolizing of TCE and VC were carried out. In addition, bioremediation of TCE and VC in contaminated saturated aquifer were studied by laboratory scale column tests, which were designed to simulate the bio-barriers under the conditions of enhancing activity of in-situ soil cells by bio-stimulation. Batch experimental results showed that the indigenous soil cells and P. putida F1 could effectively co-metabolize TCE with 100 mg/L toluene added and the removal efficiency of TCE was 87% and 94%, respectively. However, when P. putida F1 seeded to soil, the TCE removal efficiency decreased from 94% to 89% due to the competition for toluene between P. putida F1 and indigenous soil cells. Additionally, indigenous soil cells could utilize VC as a sole carbon source and the removal efficiency of VC was around 60%. It also found that the supplement of exogenous primary substrate, e.g. toluene, did not increase the degradation of VC in this study. Thus, further studies are needed to figure out if any other compatible co-substrate could enhance the co-metabolize degradation of VC by indigenous cells. Soil column tests included (1) indigenous soil column for aerobic oxidation of VC, (2) indigenous soil column for aerobic co-metabolism of TCE and (3) indigenous soil column with adding P. putida F1 for TCE co-metabolism. The test results indicated that TCE and VC would breakthrough along the columns during the initial start up period due to the lack of induced toluene dioxygenase or the low activity of microorganisms. Moreover, the dominant biodegradation occurred in the front end of the column after 20 days of operation. It observed that the concentrations of TCE and VC in the column effluent decreased with the increase of the operation time. The removal efficiencies of TCE and VC were greater than 99% after 30 days of operation. As a result, the soil columns could effectively biodegrade the contaminants when the growth of microorganisms approached to steady phase. In addition, no other chlorinated byproducts were detected while TCE and VC were biodegraded.
Chen, Yan-Min, et 陳彥旻. « Cometabolic Treatment of Trichloroethylene in Groundwater by Permeable Reactive Biobarrier ». Thesis, 2008. http://ndltd.ncl.edu.tw/handle/14185240343431472494.
Texte intégral國立成功大學
環境工程學系碩博士班
96
In this study, treatment of trichloroethylene (TCE) in contaminated groundwater was investigated using biological permeable reactive barriers (PRBs). A bacterium using phenol as the carbon and energy source, Pseudomonas putida, was employed for the cometabolic degradation of TCE. The bacterium was first investigation for its degradation kinetics of both phenol and TCE. Then, the bacterium was immobilized in chitosan beads for testing its feasibility as a PRB reactive media. Finally, an oxygen releasing material, chitosan immobilized magnesium peroxide was investigated for its applicability in PRB systems as an oxygen supplier. In the kinetic study for the cometabolic degradation of phenol and TCE, a new model was developed to simulate the experimental data. The model incorporated cell growth and decay, loss of transformation activity, competitive inhibition between growth substrate and non-growth substrate and self-inhibition of non-growth substrate was proposed to simulate the degradation kinetics of phenol and TCE by Pseudomonas putida. All the intrinsic parameters employed in this study were measured independently, and were then used for predicting the batch experimental data. The model predictions conformed well to the observed data at different phenol and TCE concentrations. At low TCE concentrations (< 2 mg/L), the models with or without self-inhibition of non-growth substrate both simulated the experimental data well. However, at higher TCE concentrations (> 6 mg/L), only the model considering self-inhibition can describe the experimental data, suggesting that a self-inhibition of TCE was present in the system. The proposed model was also employed in predicting the experimental data conducted in a repeated batch reactor, and good agreements were observed between model predictions and experimental data. The results also indicated that the biomass loss in the degradation of TCE below 2 mg/L can be totally recovered in the absence of TCE for the next cycle, and it could be used for the next batch experiment for the degradation of phenol and TCE. However, for higher concentration of TCE (> 6 mg/L), the recovery of biomass may not be as good as that at lower TCE concentrations. The degradability of phenol and TCE by Pseudomonas putida BCRC 14349 in both suspended culture and immobilized culture (the chitosan beads) systems are investigated in this study. Based on the SEM microphotos, the P. putida cells grew well on both the surface and interior of the immobilized media, and the cells were uniformly distributed in the whole bead. The degradation experiments showed that both the primary substrate, phenol, and cometabolic non-growth substrate, TCE, were able to degrade at the tested concentrations, phenol = 100 mg/L, and TCE = 0.2 - 20 mg/L. The effect of pH, between 6.7 and 10, on the degradation of both phenol and TCE may be neglected for the suspended culture system. However, for the immobilized culture system, phenol and TCE degradation were only observed at pH > 8. The different effect of pH on the degradation may be linked to the surface properties of the chitosan beads and its interaction on the activity of the bacteria. Bacteria immobilized in chitosan beads were also investigated for the effect of functional groups of the beads on the degradation of phenol in this study. The functional groups of chitosan beads forming in four different washing solutions were characterized with Fourier transform infrared (FTIR) transmission spectra. The FTIR spectra showed that the beads possess much OH groups and amine groups, and the abundance of these functional groups was affected by the washing solution used. Since the amine groups may change charge property at different pHs, the washing solutions are expected to have strong impact on the bacteria degradability. Experimental results indicated that the degradation kinetics of phenol strongly depends on the washing solution used, following the same order as the abundance of amine groups. It is expected that more abundance of amine groups at the pH tested would lead to more positively charges on the chitosan bead surface, causing inhibition of bacteria activity. In the degradation experiment, the degradation of TCE began only after the exhaustion of phenol, indicating that the competitiveness of phenol is larger than TCE. The maximum transfer yield of TCE was almost the same for the suspended and immobilized cultures (0.032 mg TCE/ mg phenol). However, the maximum transfer yields for suspended and immobilized systems occurred at different TCE concentrations. The transfer yield at higher TCE concentrations for the immobilized system may suggest that the cells immobilized in carriers were provided protection from harsh environmental conditions, and had a better tolerance to the toxicity of TCE. Oxygen released from magnesium peroxide and chitosan-immobilized oxygen release compound was studied for the dynamic at different solutions. It is observed that using MgO2 as the oxygen source will increase pH value, and the final equilibrium pH in the aquatic system depends on the buffer capacity of aquatic system. The dissolution of MgO2 and decomposition of H2O2 are both related to equilibrium pH in aquatic system and then affected the oxygen release kinetics in aquatic system. The oxygen release rates as well as the pH in the aqueous systems for the chitosan immobilized magnesium peroxide could be controlled through different manufacturing processes. Chitosan immobilized magnesium peroxide could reduce initial rate to ranges from 1/4 to 1/2 under different experimental conditions. The micro-morphology of the chitosan immobilized MgO2, using a scanning electron microscope, showed that the material is very porous. In addition, the surface area as well as diffusion resistance for oxygen transport through the chitosan beads was relevant to the manufacturing processes. This may be employed as a tool to control the release rate of oxygen. The chitsan-MgO2 beads were further studied in column experiments for testing the supply of oxygen in the degradation of phenol using the P. putida bacterium. The experiment was operated for 400 h. The data indicated a sustain degradability of phenol through the experiment. The degradation rate of column experiment was calculated as about 17 mg phenol/L/h, much larger than the control column experiment at only 2.9 mg phenol/L/h. This degradation rate is in equivalent to the data obtained from the column filled with sand and ORC® at about 17 mg phenol/L/h as well.
Kuo, Yu-chia, et 郭育嘉. « Application of in situ emulsified biobarrier to remediate chlorinated-solvent contaminated groundwater ». Thesis, 2013. http://ndltd.ncl.edu.tw/handle/5qnqqy.
Texte intégral國立中山大學
環境工程研究所
101
Soil and groundwater at many existing and former industrial areas and disposal sites is contaminated by halogenated organic compounds that were released into the environment. Halogenated organic compounds are heavier than water. When they are released into the subsurface, they tend to adsorb onto the soils and cause the appearance of DNAPL (dense-non-aqueous phase liquid) pool. Among those halogenated organic compounds, trichloroethylene (TCE) and 1,2-dichloroethane (1,2-DCA), a human carcinogen, is one of the commonly observed contaminants in groundwater. In this study, aerobic and anaerobic microcosm batch experiments were performed to evaluate the feasibility of biodegradation of 1,2-DCA by adding different growth substrates. The objective of this study was to develop the emulsified oil and apply it as the filling material in the permeable reactive barrier to remediate TCE-contaminated groundwater. In this study, the developed emulsified oil contained soybean oil, lactate, biodegradable surfactant (Simple GreenTM and lecithin), and nutrients. The emulsified oil was able to provide carbon for the enhancement of in situ anaerobic biodegradation for a long period of time. A pilot-scale study was operated at a TCE-contaminated site located in southern Taiwan. The aerobic microcosm results show that approximately 90% of 1,2-DCA removal was observed in the natural degradation group (A1) and the aerobic sludge addition group (A3) after 7 days of incubation. Up to 95% of 1,2-DCA removal could be observed in the substrate supplement group in after 14 days of incubation. In the anaerobic microcosm studies, 50% of 1,2-DCA removal could be obtained in all groups after 10 days except for the natural degradation group (B1). Moreover, the degradation efficiency for the anaerobic sludge group (B3) reached 80% of 1,2-DCA removal in 5 days. The DGGE profiles show that the microbial diversity varied with time and the sugar supplement groups (A2, B2) exhibited the most microbial diversity. Bacterial clones results revealed that the 1,2-DCA biodegradable microbial strains were presented in the microcosms, such as Klebsiella, Pseudomonas, Rhodoferax and Xanthobactor. The real-time PCR results indicated that the Dehalococcoides spp. was the major bacterium that was responsible for the degradation of 1,2-DCA in the anaerobic substrate supplement group (B2). Desulfitobacterium spp. could be the dominant 1,2-DCA degrading bacterium for the aerobic substrate supplement group (A2) and all of the anaerobic groups (B1, B2, B3, B4). Emulsified oil emulsion was pressure-injected into the remediation wells. Based on the groundwater analytical results, dissolved oxygen, oxidation-reduction potential, and sulfate concentrations decreased after injection. However, the anaerobic degradation byproduct, acetic acid, increased after injection. Results also show that the total viable bacteria increased in the upgradient injection (remediation) well. Decrease in TCE concentration (dropped to below 0.01 mg/L) was also observed after substrate injection, and TCE degradation byproducts, cis-1,2-dichloroethene (cDCE) and vinyl chloride (VC) were also observed. Result of microbial analyses show that various TCE-degrading bacteria exist in the groundwater samples including Ralstonia sp., Clostridium sp., Uncultured Burkholderiales bacterium, Hydrogenophaga sp., Acidovorax sp., Zoogloea sp., Hydrocarboniphaga sp., Uncultured Curvibacter sp., Pseudomonas sp., Comamonas sp., Aquabacterium sp., and Variovorax strains. This reveals that the anaerobic dechlorination of TCE is a feasible technology at this site. Slug test result show that only a slight variation in soil permeability of the injection well was observed. This indicates that the developed system has the potential to be developed into an environmentally, economically, and naturally acceptable remedial technology. Knowledge obtained from this study will aid in designing a emulsified biobarrier system for site remediation.
Liang, Shu-hao, et 梁書豪. « Development of in situ oxidative-barrier and biobarrier to remediate organic solvents-contaminated groundwater ». Thesis, 2011. http://ndltd.ncl.edu.tw/handle/11498760542269300115.
Texte intégral國立中山大學
環境工程研究所
100
Soil and groundwater at many existing and former industrial areas and disposal sites is contaminated by organic solvent compounds that were released into the environment. Organic solvent compounds are heavier than water. When they are released into the subsurface, they tend to adsorb onto the soils and cause the appearance of LNAPL (light nonaqueous phase liquid) and DNAPL (dense nonaqueous phase liquid) pool. The industrial petroleum hydrocarbons (e.g., methyl tertiary-butyl ether, MTBE and benzene) and chlorinated solvent (e.g., trichloroethylene, TCE) are among the most ubiquitous organic compounds found in subsurface contaminated environment. One cost-effective approach for the remediation of the chlorinated solvent and petroleum products contaminated aquifers is the installation of permeable reactive zones or barriers within aquifers. As contaminated groundwater moves through the emplaced reactive zones, the contaminants are removed, and uncontaminated groundwater emerges from the downgradient side of the reactive zones. The objectives of this study were developed to evaluate the feasibility of applying in-situ chemical oxidation (ISCO) barrier and in-situ slow polycolloid-releasing substrate (SPRS) biobarrier system on the control of petroleum hydrocarbons and chlorinated solvent plume in aquifer. In the ISCO barrier system, it contained oxidant-releasing materials, to release oxidants (e.g., persulfate) contacting with water for oxidating contaminants existed in groundwater. In this study, laboratory-scale fill-and-draw experiments were conducted to determine the compositions ratios of the oxidant-releasing materials and evaluate the persulfate release rates. Results indicate that the average persulfate-releasing rate of 7.26 mg S2O82-/d/g was obtained when the mass ratio of sodium persulfate/cement/sand/water was 1/1.4/0.24/0.7. The column study was conducted to evaluate the efficiency of in situ application of the developed ISCO barrier system on MTBE and benzene oxidation. Results from the column study indicate that approximately 86-92% of MTBE and 95-99% of benzene could be removed during the early persulfate-releasing stage (before 48 pore volumes of groundwater pumping). The removal efficiencies for MTBE and benzene dropped to approximately 40-56% and 85-93%, respectively, during the latter part of the releasing period due to the decreased persulfate-releasing rate. Results reveal that acetone, byproduct of MTBE, was observed and then further oxidized completely. Results suggest that the addition of ferrous ion would activate the persulfate oxidation. However, excess ferrous ion would compete with organic contaminants for persulfate, causing the decrease in contaminant oxidation rates. In the SPRS biobarrier system, the food preparation industry has tremendous experiences in producing stable oil-in-water (W/O, 50/50) emulsions with a uniformly small droplet size. Surfactant mixture (71 mg/L of SL and 72 /L of SG) blending with water could yield a stable and the optimal emulsion was considered the best. The small absolute value of the emulsion zeta potential reduces inter-particle repulsion, causing the emulsion droplets to stick to each other when they collided. Overtime, large masses of flocculated droplets can form which then clog the sediment pores. The results can be used to predict abiotic interactions and distribution of contaminant mass expected after SPRS injection, and thus provides a more accurate estimate of the mass of TCE removed due to enhanced biodegradation. The effect of TCE partitioning to the vegetable oil on contaminant migration rates can be approximated using a retardation factor approach, where 0.28 years through a 3 m barrier. In anaerobic microcosm experiments, result show that SPRS can be fermented to hydrogen and acetate could be used as a substrate to simulate reductive dehalorination. The apparent complete removal of nitrate and sulfate by SPRS addition was likely a major factor that promoted the complete reduction of TCE at later stages of this study. Results from the column experiment indicate that occurrence of anaerobic reductive dechlorination in the biobarrier system can be verified by: (1) the oil: water partition coefficients of dissolved TCE into vegetable oil were be used to predict abiotic interactions and distribution of contaminant mass expected after SPRS injection. (2) The SPRS can ferment to hydrogen and acetate could be used as a substrate to simulate reductive dechlorination. The proposed treatment scheme would be expected to provide a more cost-effective alternative to remediate other petroleum hydrocarbons and chlorinated solvents-contaminated aquifers. Experiments and operational parameters obtained from this study provide an example to design a passive barriers system for in-site remediation.
Livres sur le sujet "Biobarriera"
International In Situ and On-Site Bioremediation Symposium (6th 2001 San Diego, Calif.). Bioaugmentation, biobarriers, and biogeochemistry : The Sixth International In Situ and On-Site Bioremediation Symposium : San Diego, California, June 4-7, 2001. Sous la direction de Leeson Andrea 1962-. Columbus, Ohio : Battelle Press, 2001.
Trouver le texte intégralCalif.) International In Situ and On-Site Bioremediation Symposium (6th : 2001 : San Diego. Bioaugmentation, Biobarriers, and Biogeochemistry : The Sixth International in Situ and On-Site Bioremediation Symposium : San Diego, California, June 4-7, ... in Situ and On-Site Bioremediation Sympo). Battelle Press, 2001.
Trouver le texte intégralChapitres de livres sur le sujet "Biobarriera"
Conley, Catharine A. « Biobarrier ». Dans Encyclopedia of Astrobiology, 159. Berlin, Heidelberg : Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_164.
Texte intégralConley, Catharine A. « Biobarrier ». Dans Encyclopedia of Astrobiology, 261. Berlin, Heidelberg : Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_164.
Texte intégralConley, Catharine A. « Biobarrier ». Dans Encyclopedia of Astrobiology, 1. Berlin, Heidelberg : Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_164-2.
Texte intégralSpry, J. Andy. « Biobarrier ». Dans Encyclopedia of Astrobiology, 1. Berlin, Heidelberg : Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_5571-1.
Texte intégralSpinnler, Gerard E., Paul M. Maner, Jeffrey D. Stevenson, Joseph P. Salanitro, Jennifer Bothwell et John Hickey. « Application of an In Situ Bioremedy Biobarrier at a Retail Gas Station ». Dans MTBE Remediation Handbook, 517–27. Boston, MA : Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0021-6_28.
Texte intégralAshraf, M. A., S. Batool, M. Ahmad, M. Sarfraz et W. S. A. W. M. Noor. « Biopolymers as biofilters and biobarriers ». Dans Biopolymers and Biotech Admixtures for Eco-Efficient Construction Materials, 387–420. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-08-100214-8.00017-8.
Texte intégralKuippers, Gina, Naji M. Bassil et Jonathan R. Lloyd. « Microbial colonization of cementitious geodisposal facilities, and potential “biobarrier” formation ». Dans The Microbiology of Nuclear Waste Disposal, 157–92. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-818695-4.00008-3.
Texte intégralFrieboes, Hermann B., Paolo Decuzzi, John P. Sinek, Mauro Ferrari et Vittorio Cristini. « Computational Modeling of Tumor Biobarriers : Implications for Delivery of Nano-Based Therapeutics ». Dans Nanomedicine, 201–44. Jenny Stanford Publishing, 2019. http://dx.doi.org/10.1201/9780429065767-6.
Texte intégralActes de conférences sur le sujet "Biobarriera"
Soodmand, alireza, Seyed Ahmad Farzad Shariatpanahi, Hossein Emadi et Behrooz Roozbehani. « Ground Biobarrier Formation for Preventing Contamination Migration ». Dans Middle East Health, Safety, Security, and Environment Conference and Exhibition. Society of Petroleum Engineers, 2010. http://dx.doi.org/10.2118/136089-ms.
Texte intégralden Baars, P. Scott, John P. Kaszuba, Ted Cota, Jonathan Myers, Patrick Longmire, Betty A. Strietelmeier et Tammy P. Taylor. « Design and Construction of Multi-Layered Permeable Reactive Barrier for Removing Radionuclides, Nitrate, and Perchlorate at Los Alamos National Laboratory ». Dans ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-5002.
Texte intégralSaponaro, S., A. Careghini, L. Romele, E. Sezenna, A. Franzetti, I. Gandolfi, M. Daghio et G. Bestetti. « Remediation of groundwater polluted by gasoline-derived compounds with biobarriers ». Dans WATER POLLUTION 2012. Southampton, UK : WIT Press, 2012. http://dx.doi.org/10.2495/wp120381.
Texte intégralKatsenovich, Y., Z. Ozturk, M. Allen, B. Tansel et G. Wein. « Enhancing TCE Biodegradation by Using Agricultural Byproducts in Biobarrier System ». Dans World Environmental and Water Resources Congress 2007. Reston, VA : American Society of Civil Engineers, 2007. http://dx.doi.org/10.1061/40927(243)319.
Texte intégralBruce, C. L., et P. C. Johnson. « Application of a BioBarrier to a mixed MTBE/BTEX dissolved plume ». Dans Environmental Health Risk 2001. Southampton, UK : WIT Press, 2001. http://dx.doi.org/10.2495/ehr010171.
Texte intégralRapports d'organisations sur le sujet "Biobarriera"
Tollner, E. W., et C. E. Jr Murphy. Measuring the efficacy of a root biobarrier with x-ray computed tomography. Office of Scientific and Technical Information (OSTI), août 1990. http://dx.doi.org/10.2172/6174456.
Texte intégralJohnson, Paul C., Karen D. Miller et Cristin L. Bruce. A Practical Approach to the Design, Monitoring, and Optimization of the Situ MTBE Aerobic Biobarriers. Fort Belvoir, VA : Defense Technical Information Center, décembre 2004. http://dx.doi.org/10.21236/ada429040.
Texte intégralB.D. Wood. Influence of Reactive Transport on the Reduction of U(VI) in the Presence of Fe(III) and Nitrate : Implications for U(VI) Immobilization by Bioremediation / Biobarriers- Final Report. Office of Scientific and Technical Information (OSTI), janvier 2007. http://dx.doi.org/10.2172/902115.
Texte intégral