Numerical models (GMS MODFLOW, SEAM3D, and SEAM3D Interface) were applied to simulate groundwater flow, petroleum hydrocarbon compound (PHC) transport and biodegradation, and the transport and biotransformation of chlorinated ethenes at Site FT-002 Plattsburgh Air Force Base (PAFB), NY. Site FT-002 was contaminated with waste jet fuel and chlorinated ethenes used as a fire source during fire fighting training. The results of groundwater analysis indicated that the aquifer exhibited aerobic, nitrate reducing, ferrogenic, sulfate reducing and methanogenic conditions due to the biodegradation of the PHCs. Additional groundwater analysis showed the biotransformation of TCE to DCE, VC, and ethene. A numerical model was developed to simulate and assess the extent to which reductive dechlorination and direct anaerobic oxidation were responsible for the biotransformation of the chlorinated ethenes. Reductive dechlorination accounted for the 100%, 98.3%, and 97.5% of the biotransformation of TCE, DCE, and VC respectively. Direct anaerobic oxidation accounted for 1.7% and 2.5% of the biotransformation of DCE and VC respectively. Though direct anaerobic oxidation only accounted for a small percentage of total biotransformation it was necessary to fully develop the biotransformation of the DCE and VC in the ferrogenic zone. This study focused on the mechanisms responsible for the biotransformation of chlorinated ethenes, specifically reductive dechlorination and direct anaerobic oxidation. By further defining the NAPL source and initial conditions it could be used as a tool to accurately predict the monitored natural attenuation (MNA) of the FT-002 contaminant plume. / Master of Science

The reduction of manufacturing costs and the facilitation of direct-oxidation of hydrocarbon fuels have been identified as means of promoting the commercialization of the solid oxide fuel cell, a technology that offers both environmental and fuel conservation benefits compared to conventional energy conversion technologies. This research was conducted with the aim of realizing the production of direct-oxidation anodes using atmospheric plasma spraying, which has been identified as a fabrication technique that has the potential to reduce the manufacturing costs of solid oxide fuel cells. This thesis details the rationale behind the selection of the anode compositions (BaO-Ni-YSZ, CeO2-Ni-YSZ, and Sn-Ni-YSZ) and the specifics of the specialized fabrication strategy (SPS-SPPS) that was devised with the aim of realizing microstructures similar to those where the secondary phases (BaO, CeO2, and Sn) coat the surfaces of the primary Ni and YSZ phases. Results of XRD, SEM and EDS analyses are presented.

The reduction of manufacturing costs and the facilitation of direct-oxidation of hydrocarbon fuels have been identified as means of promoting the commercialization of the solid oxide fuel cell, a technology that offers both environmental and fuel conservation benefits compared to conventional energy conversion technologies. This research was conducted with the aim of realizing the production of direct-oxidation anodes using atmospheric plasma spraying, which has been identified as a fabrication technique that has the potential to reduce the manufacturing costs of solid oxide fuel cells. This thesis details the rationale behind the selection of the anode compositions (BaO-Ni-YSZ, CeO2-Ni-YSZ, and Sn-Ni-YSZ) and the specifics of the specialized fabrication strategy (SPS-SPPS) that was devised with the aim of realizing microstructures similar to those where the secondary phases (BaO, CeO2, and Sn) coat the surfaces of the primary Ni and YSZ phases. Results of XRD, SEM and EDS analyses are presented.

Solid oxide fuel cells (SOFCs) that operate directly on hydrocarbon fuels eliminate the requirement for costly and complex external reforming systems. Atmospheric plasma spraying (APS) is an established manufacturing method that offers the potential to fabricate direct oxidation SOFC anodes in a single step, instead of the multiple steps currently required. Manufacturing by APS also allows the use of metal supports, which improve thermal shock resistance, allow rapid cell heat-up, and reduce total cost. In this study, direct oxidation SOFC anodes based on Cu and samaria-doped ceria (SDC) in combination with Co and/or Ni were investigated for their stability and performance in H2 and CH4 when plasma sprayed on ferritic stainless steel supports. Several different APS techniques were investigated. Two of these techniques were hybrid methods involving a combination of dry powder plasma spray and suspension plasma spray (SPS) processes. These techniques were proposed to help balance the degree of melting of the lower melting temperature oxides of the metals Cu, Co, and Ni with that of the higher melting temperature SDC. The use of a single suspension containing all of the anode component feedstocks was also investigated. Multi-component aqueous suspensions of CuO, Co3O4, and NiO were developed with or without the addition of carbon black and SDC. It was found that the use of a hybrid plasma spray technique can help to improve deposition efficiency (D.E.) and enhance partial melting of the low melting temperature feedstocks. However, plasma spraying all of the components in a single suspension can lead to more homogeneous mixing and greater resistance to metal coarsening at SOFC operating temperatures. In electrochemical tests of plasma-sprayed metal-supported cells containing these anodes, peak power densities as high as 0.6 W/cm2 were achieved at 750 deg C in humidified H2. In CH4, power density was limited by the activity of the anodes. Stability in CH4 was poor because of oxidation of the metal support and enhanced coking behaviour resulting from interactions between Fe in the support and Co and Ni in the anodes. When separated from the supports, the anodes demonstrated very low coking rates in thermogravimetric analysis experiments in CH4.

Solid oxide fuel cells (SOFCs) that operate directly on hydrocarbon fuels eliminate the requirement for costly and complex external reforming systems. Atmospheric plasma spraying (APS) is an established manufacturing method that offers the potential to fabricate direct oxidation SOFC anodes in a single step, instead of the multiple steps currently required. Manufacturing by APS also allows the use of metal supports, which improve thermal shock resistance, allow rapid cell heat-up, and reduce total cost. In this study, direct oxidation SOFC anodes based on Cu and samaria-doped ceria (SDC) in combination with Co and/or Ni were investigated for their stability and performance in H2 and CH4 when plasma sprayed on ferritic stainless steel supports. Several different APS techniques were investigated. Two of these techniques were hybrid methods involving a combination of dry powder plasma spray and suspension plasma spray (SPS) processes. These techniques were proposed to help balance the degree of melting of the lower melting temperature oxides of the metals Cu, Co, and Ni with that of the higher melting temperature SDC. The use of a single suspension containing all of the anode component feedstocks was also investigated. Multi-component aqueous suspensions of CuO, Co3O4, and NiO were developed with or without the addition of carbon black and SDC. It was found that the use of a hybrid plasma spray technique can help to improve deposition efficiency (D.E.) and enhance partial melting of the low melting temperature feedstocks. However, plasma spraying all of the components in a single suspension can lead to more homogeneous mixing and greater resistance to metal coarsening at SOFC operating temperatures. In electrochemical tests of plasma-sprayed metal-supported cells containing these anodes, peak power densities as high as 0.6 W/cm2 were achieved at 750 deg C in humidified H2. In CH4, power density was limited by the activity of the anodes. Stability in CH4 was poor because of oxidation of the metal support and enhanced coking behaviour resulting from interactions between Fe in the support and Co and Ni in the anodes. When separated from the supports, the anodes demonstrated very low coking rates in thermogravimetric analysis experiments in CH4.

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