Spelling suggestions: "subject:"bioremediation"" "subject:"biorremediation""
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Alkaline hydrolysis of explosivesVanEngelen, Catherine Elizabeth. January 1900 (has links) (PDF)
Thesis (PhD)--Montana State University--Bozeman, 2009. / Typescript. Chairperson, Graduate Committee: Brent M. Peyton. Includes bibliographical references.
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Measurements and mechanisms of microbial PAH bioremediation in undisturbed marine sediments /Tang, Yinjie, January 2004 (has links)
Thesis (Ph. D.)--University of Washington, 2004. / Vita. Includes bibliographical references (leaves 249-266).
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Bioreduction of hexavalent chromium flow-through column experiments and reactive transport modeling /Alam, Md Mahbub, January 2004 (has links) (PDF)
Thesis (Ph. D. in Civil Engineering)--Washington State University. / Includes bibliographical references.
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2-Chloroacetophenone as a probe compound for studying reduction reactions in anaerobic sediments /Reilkoff, Thea E., January 2000 (has links)
Thesis, (M.S.)--Oregon Graduate Institute, 2000.
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Plant-assisted bioremediation of perchlorate and the effect of plants on redox conditions and biodiversity in low and high organic carbon soilStruckhoff, Garrett Cletus. Parkin, Gene F. January 2009 (has links)
Thesis supervisor: Gene F. Parkin. Includes bibliographic references (p. 117-125).
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Response to osmotic stress by the haloalkaliphilic bacterium Halomonas campisalisAston, John, January 2006 (has links) (PDF)
Thesis (M.S. in chemical engineering)--Washington State University, May 2006. / Includes bibliographical references (p. 66-74).
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Continuous bioremediation of electroplating effluentSantos, Bruno Alexandre Quistorp January 2013 (has links)
Thesis submitted in fulfilment of the requirements for the degree
Magister Technologiae: Chemical Engineering
in the Faculty of
Engineering
at the
Cape Peninsula University of Technology
2013 / There are significant quantities of free cyanide (F-CN) and heavy metal contaminated effluent being discharged from electroplating operations globally. However, there is an overwhelming tendency in the industry to use physical and/or chemical treatment methods for cyanides (CNs) and heavy metals in effluent. Although these methods may be effective for certain CNs and heavy metals, they produce toxic by-products and also involve high operational and capital investment costs when compared to bioremediation methods. In this study, the design of a two-stage membrane bioreactor (MBR) system was conceptualised for the bioremediation of CNs and heavy metals in the effluent which was collected from an electroplating facility located in the Western Cape, South Africa. The design included a primary inactive bioremediation stage, to reduce the impact of contaminate concentration fluctuations, and a secondary active bioremediation stage, to remove the residual contaminants, in the effluent under alkaline pH conditions which typify most industrial effluent containing these contaminants. An analysis of the electroplating effluent revealed that the effluent contained an average of 149.11 (± 9.31) mg/L, 5.25 (± 0.64) mg/L, 8.12 (± 4.78) mg/L, 9.05 (± 5.26) mg/L and 45.19 (± 25.89) mg/L of total cyanide (T-CN), F-CN, weak acid dissociable cyanides (WAD-CNs), nickel (Ni), zinc (Zn) and copper (Cu), respectively.
An Aspergillus sp., which displayed the characteristic black conidiophores of the Aspergillus section Nigri, was isolated from the electroplating facilities’ effluent discharge using a selective pectin agar (PA) and subcultured on 2% (v/v) antibiotic (10,000 units/L penicillin and 10 mg streptomycin/mL) potato dextrose agar (PDA). The isolate was tolerant to F-CN up to 430 mg F-CN/L on F-CN PDA plates which were incubated at 37 ˚C for 5 days. However, a significant decline in microbial growth was observed after 200 mg F-CN/L, thus indicating that the isolate was suitable for the bioremediation of the electroplating effluent. The identification of the isolate as Aspergillus awamori (A. awamori) was definitively determined using a multi-gene phylogenetic analysis, utilising ITS (internal transcribed spacer), -tubulin and calmodulin gene regions. Although an anomaly in the morphology of the conidia of the isolate was observed during the morphological analysis, indicating a possible morphological mutation in the isolate. A comparative study between “sweet orange” (Citrus sinensis (C. sinensis)) pomace, “apple” (Malus domestica (M. domestica)) pomace, “sweetcorn” (Zea mays (Z. mays)) cob and “potato” (Solanum tuberosum (S. tuberosum)) peel, i.e. waste materials considered to be agricultural residues, was conducted in order to assess their potential and as a sole carbon source supplement for A. awamori biomass development for the bioremediation of CNs and heavy metals.
The suitability of these agricultural residues for these activities were as follows: C. sinensis pomace ˃ M. domestica pomace ˃ Z. mays cob ˃ S. tuberosum peel. For purpose of the sensitivity analysis, a temperature range of 20 to 50 ˚C and an alkaline pH range of 7 to 12 showed that: (1) optimal conditions for the uptake of Ni, Zn and Cu occurred at pH 12 and a temperature of 37.91 and 39.78 ˚C using active and inactive A. awamori biomass and unhydrolysed and hydrolysed C. sinensis pomace, respectively; (2) F-CN conversion increased linearly with an increase in pH and temperature using unhydrolysed and hydrolysed C. sinensis pomace; and (3) optimal conditions for the F-CN conversion and the respective by-products and sugar metabolism using active A. awamori biomass occurred at 37.02 ˚C and pH 8.75 and at conditions inversely proportional to F-CN conversion, respectively. The heavy metal affinity was Ni > Zn > Cu for all the biomaterials used and with the heavy metal uptake capacity being inactive A. awamori biomass > active A. awamori biomass > hydrolysed C. sinensis pomace > unhydrolysed C. sinensis pomace, respectively. Hydrolysed C. sinensis pomace had a 3.86 fold higher conversion of F-CN compared to the unhydrolysed C. sinensis pomace. The use of C. sinensis pomace extract as a nutrient media, derived from the acid hydrolysis of C. sinensis pomace, showed potential as a rich carbon-based supplement and also that low concentrations, < 0.1% (v/v), were required for the bioremediation of CNs and heavy metals.
The two-stage MBR system was operated at 40 ˚C since this temperature was conducive to the bioremediation of CN and heavy metals. The primary bioremediation stage contained hydrolysed C. sinensis pomace while the secondary bioremediation stage contained active A. awamori biomass, supplemented by the C. sinensis pomace extract. After the primary and secondary bioremediation stages, 76.37%, 95.37%, 93.26% and 94.76% (primary bioremediation stage) and 99.55%, 99.91%, 99.92% and 99.92% (secondary bioremediation stage) average bioremediation efficiencies for T-CN, Ni, Zn and Cu were achieved. Furthermore, the secondary bioremediation stage metabolised the CN conversion by-products with an efficiency of 99.81% and 99.75% for formate (CHOO-) and ammonium (NH4+), respectively. After the first, second and third acid regeneration cycles of the hydrolysed C. sinensis pomace, 99.13%, 99.12% and 99.04% (first regeneration cycle), 98.94%, 98.92% and 98.41% (second regeneration cycle) and 98.46%, 98.44% and 97.91% (third regeneration cycle) recovery efficiencies for Ni, Zn and Cu were achieved. However, the design only managed to treat the effluent for safe discharge and the use of a post-treatment stage, such as reverse osmosis, is recommended to remove the remainder of the trace contaminants and colour from the effluent to ensure that the effluent met the potable water standards for reuse. There was a relatively insignificant standard deviation (≤ 3.22%) detected in all the parameters measured in the continuous operation and this indicates the reproducibility of the bioremediation efficiency in this continuous system.
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The biogeochemical behaviour of plutonium and americium in contaminated soilsKimber, Richard January 2012 (has links)
The biogeochemical behaviour of plutonium and americium was investigated in contaminated soils from the UK to help determine possible remediation and management options. Stimulating anoxic sediments from Aldermaston, through the addition of a carbon substrate (glucose), induced reducing conditions resulting in a negligible change in Pu mobility. This was despite a substantial shift in the bacterial profile from a diverse community to one dominated by fermentative Beta proteobacteria and Clostridia. The latter group also includes organisms associated with metal reduction, such as close relatives to Clostridium species, reported previously to facilitate the reduction of Pu(IV) to Pu(III). A sequential extraction was performed on soils from Aldermaston and the Esk Estuary to identify which selected fractions the Pu and Am are most strongly associated with. The majority of Pu was associated with the 'residual fraction': 63.8 – 85.5 % and 91.9 – 94.5 % in the Aldermaston and Esk Estuary soils respectively. Metals associated with this fraction are highly recalcitrant and are unlikely to be released into solution over a significant time span under most geological conditions. The Am was more evenly distributed with the 'organic fraction' being the most dominant. Degradation of organic matter under oxidising conditions may result in mobilization of metals associated with this fraction. The Aldermaston soil was also subjected to bioleaching using a sulfuric acid producing microbial community, which resulted in a maximum 0.18 % of Pu released into solution. However, up to 12.5% of Am was found in solution suggesting Am is more susceptible to mobilization than Pu. The potential for Pu mobilization through abiotic oxidative leaching was investigated using permanganate. Even when carbonate was added to act as a potential complexant for the Pu, less than 1% of the Pu was leached. Greater success was observed when leaching was attempted using citric acid; an estimated 25 – 30% of Pu was released into solution offering a potential route for remediation of Pu-contaminated soils. These data would suggest that the Pu is highly recalcitrant, and may exist in a small particulate form in the Aldermaston soils, possibly in the oxide form, and is unlikely to mobilize under natural biogeochemical conditions.
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Dissipation and Leachability of Formulated Chlorpyrifos and Atrazine in Organically-amended SoilsXiao, Yunxiang III 10 December 1997 (has links)
Bioremediation was studied in soils containing high concentrations of formulated chlorpyrifos (5 mg kg-1 Dursban® 4E) and atrazine (5 mg kg-1 AAtrex® 4L) using amendments including lignocellulosic sorbents, microbial nutrients (vegetable oil, corn meal and fertilizers), and microbial extracts from organic media previously exposed to these pesticides (chlorpyrifos and atrazine, respectively). Radiolabeled atrazine was used to examine the various dissipation routes in contaminated soil, also amended with lignocellulosic sorbents and microbial nutrients.
Both chlorpyrifos and atrazine dissipation from contaminated soils was enhanced by organic-based material amendments. The half-lives of chlorpyrifos based on extractability for soils unamended and amended with vegetable oil and peat moss were 87 and 52 days, respectively. The half-lives of atrazine in unamended and amended soil (vegetable oil, peat moss and fertilizers) were 175 and 40 days, respectively. The leachability of chlorpyrifos from contaminated soil was dramatically reduced by 82% during the first 30 days of incubation in treatments amended with vegetable oil and peat moss while only a 28% of reduction in leachability occurred in the corresponding unamended controls. Only a slight reduction of atrazine leachability was detected in amended treatments after 120 days of incubation.
Differences were found in the leachability of chlorpyrifos and atrazine when they were applied to soil either as technical grade or formulated material. The presence of surfactants and other adjuvants in formulated chlorpyrifos (Dursban® 4E) reduced chlorpyrifos leachability in contaminated soil. Chlorpyrifos leachability was reduced by 43% in the formulated chlorpyrifos treatments, whereas there was a negligible decrease in technical chlorpyrifos treated soil during the first 3 days after contamination. Atrazine extractability and leachability was not affected by its formulation (AAtrex® 4L).
Amendments with lignocellulosic sorbents and nutrients decreased atrazine®s volatility from contaminated soils. After 16 weeks of incubation, less than 1% of 14C-atrazine was volatilized from incubated soils. Overall, after 16 weeks of incubation less than 4% of 14C-atrazine was mineralized and more radioactivity was recovered from amended treatments than unamended treatments as 14CO2. The major portion of radioactivity (62%) was associated with physisorbed atrazine represented by the ethylacetate extract I from unamended treatments while only 28% of initial applied radioactivity was recovered in the corresponding amended treatments. Based on the sum of radioactivity in humic and fulvic acids, approximately 14% of radioactivity was incorporated or chemisorbed atrazine and its metabolites in both unamended and amended treatments. Forty-five percent of the initially applied radioactivity was associated with alkali insoluble fraction in amended treatments but only 17% of the initially applied radioactivity was detected in the corresponding unamended treatments. Less than 2 % of initial activity associated with physisorbed portions of fulvic acids and alkaline insoluble fraction indicated as the radioactivity in methylene chloride and ethylacetate extract II . Over time, more radioactivity was associated with polar atrazine hydroxylated degradation products. / Ph. D.
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Assessment of bacterial communities and an iron-reducing bacterium in relation to an engineered bioremediation system designed for the treatment of uranium-nitric acid contaminated groundwaterHwang, Chiachi 01 May 2009 (has links)
No description available.
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