For enhanced or Engineered Geothermal Systems (EGS) geothermal brine is pumped to the surface via the production wells, the heat extracted to turn a turbine to generate electricity, and the spent brine re-injected via injection wells back underground. If designed properly, the subsurface rock formations will lead this water back to the extraction well as heated brine. Proper monitoring of these geothermal reservoirs is essential for developing and maintaining the necessary level of productivity of the field. Chemical tracers are commonly used to characterize the fracture network and determine the connectivity between the injection and production wells. Currently, most tracer experiments involve injecting the tracer at the injection well, manually collecting liquid samples at the wellhead of the production well, and sending the samples off for laboratory analysis. While this method provides accurate tracer concentration data at very low levels of detection, it does not provide information regarding the location of the fractures which were conducting the tracer between wellbores. Sandia is developing a high-temperature electrochemical sensor capable of measuring tracer concentrations and pH downhole on a wireline tool. The goal of this effort is to collect real-time pH and ionic tracer concentration data at temperatures up to 225 °C and pressures up to 3000 psi. In this paper, a prototype electrochemical sensor and the initial data obtained will be presented detailing the measurement of iodide tracer concentrations at high temperature and pressure in a newly developed laboratory scale autoclave.
Growth and electrochemical and optical properties of single crystalline vanadium pentoxide (V2O5) nanorod arrays were investigated. Vanadium pentoxide nanorod arrays were grown by electrochemical deposition, surface condensation induced by a pH change and sol electrophoretic deposition. Uniformly sized vanadium oxide nanorods with a length of about 10μm and diameters of 100 or 200nm were grown over a large area with near unidirectional alignment. TEM micrographs and electron diffraction patterns of V2O5 nanorods clearly show the single-crystalline nature of nanorods from all three growth routes with a growth direction of [010]. The growth mechanisms of single crystal vanadium pentoxide nanorods have been discussed. The transmittance of nanorod arrays decrease more quickly under applied electric field than sol-gel derived film, which suggests nanorod array electrodes possess significantly improved charge/discharge rate. Electrochemical analysis is proves that nanorod arrays have higher efficiency than sol-gel derived film. The relationships between electrochemical and optical properties, nano and microstructures, and growth mechanisms have been discussed.
Nanomaterials are advantageous for photoelectrochemical solar cell devices for high efficient conversion of light to electrical power due to its large surface area at which photoelectrochemical processes take place. One of the current solar cell systems utilizes dye-functionalized mesoporous titania films that consist of an interconnected network of nanometer-sized crystals. This type of structure imparts a large surface area for efficient dye adsorption and, thus, efficient electron-hole formation. This structure formed with connected nanoparticles possesses mesoscopic pores with an irregular and non-uniform pore structure. Such a structure imparts two problems: the transport of electrons through such a random structure, particularly through the necks between two particles, may become a limiting step, and the irregular mesoporous structure may not be ideal for dye assembly. In addition, a liquid electrolyte has to be used to accommodate such irregular mesoporous structures. In this paper, we propose to explore and present some preliminary results of ordered dye-functionalized titania nanostructures for potential enhancement of electron percolation pathways and light conversion. Such dye-sensitized, uniformly-sized, and unidirectionally-aligned titania nanorods and indium-tin-oxide nanorods coated with a titania layer have been synthesized and characterized for discussion.
Template-based growth of single crystal V2O5 nanorods by either electrochemical or electrophoretic deposition was studied. Specifically, standard electrochemical deposition from VOSO4 solution, electrochemically induced deposition by local pH change of VO2+ solution, and electrophoretic deposition of nanoclusters in V2O5 sol were investigated. From each route, uniformly sized V2O5 nanorods about 10 μm in length were grown over large area with nearly unidirectional alignment, but with various extent of lateral shrinkage when fired at 500°C. These grown V2O5 nanorods all have the same single-crystal structure, regardless of deposition method and initial solutions or sol used.
Electrochromic materials are of interest for a wide variety of applications, such as displays and smart windows. Many electrochromic oxide materials are synthesized through sol-gel processing. We have demonstrated a general technique for the synthesis of oxide nanorods using sol electrophoretic deposition with an appropriate template. This technique can be applied for the synthesis of nanorods of electrochromic materials, such as TiO2, V2O5 and Nb2O5, with diameters of ~100 nm and a length of ~10 μm. By attaching these nanorods to a conducting substrate (such as ITO coated glass), it is possible to characterize the electrochromic behavior of these materials via UV-Vis absorbance spectroscopy. A similar technique has been used to make nanorods of the transparent conducting oxide indium tin oxide (ITO), which is often used as a working electrode in electrochromic devices. Such ITO nanorods have diameters of ~75-140 nm and lengths up to 60 μm.
Optically transparent superhydrophobic silica-based coatings were obtained by means of sol-gel processing and self-assembling. Superhydrophobicity was achieved through a combination of enhanced surface roughness by incorporating nanoclusters and modification of surface chemistry by self-assembly. The self-assembly monolayer (SAM) was prepared using the chemical coupling reaction between chlorosilyl groups and hydroxylated coating surface. The optical transparence of such hydrophobic coatings was found to be higher than 95%, which is attributed to the fact that the roughness scale is too small to scatter the visible light. The water contact angle was of approximately 150°.
Metal-insulator core-shell structures have been demonstrated to have interesting and tunable optical properties. Systems previously investigated include silica-capped gold particles and gold shells surrounding silica particles. However, many of the systems studied so far have been spherical (or zero-dimensional). Thus, it would be of interest to look at the synthesis and optical properties of one-dimensional (i.e., rod-like) nanostructures. In this paper, the authors present and discuss the formation and properties of silica and titania nanorods encapsulated with a thin gold shell. Nanorods of silica and titania ~10 μm in length and with diameters ~ 90-200 nm are made by combining sol-gel electrophoresis with a suitable template. After removing the template at high temperature, the surface of the rods is re-hydrolyzed by heating in water. 3-Aminopropyltrimethoxysilane is reacted with the surface hydroxyl groups, self-assembling amine functionality on the surface of the rods. These groups act as anchoring sites for the gold, which forms a thin shell around the oxide nanorod. UV-vis absorbance spectra of these samples are analyzed to determine the relationships between shell thickness, core size, core material and properties.
Dye-functionalized mesoporous silica has gained considerable attention for use in optical applications. Much interest into the tunable functionality of these small-scale optical materials has been the focus for possible use in lasers, light filters, sensors, solar cells, and photocatalysis. Extensive exploration into functionalizing mesoporous silica has been made using sol-gel methods for incorporating polymeric dyes within the pore channels of the silica network to modify optical properties. However, research so far has been focused on functionalization of mesoporous silica powders or films on dense substrates, limiting applications in practice because of the difficult accessibility of mesopores. In this paper, we studied the development of hierarchically-structured mesoporous silica with chromophore dye molecules covalently linked within the channel walls of pores for the selective adsorption and detection of specific ions and chemical compounds. Hierarchically-structured, unidirectionally-aligned mesoporous silica was synthesized within the pores of polycarbonate membranes by surfactant-assisted sol electrophoretic deposition. After the removal of surfactants from the mesopores, the inner surface of the mesopores was functionalized with silane-containing chromophore molecules through self-assembly. Full coverage of these dye molecules on the surface of the mesopores was anticipated due to the fact that these reactant chromophore molecules, in solution, migrate through the pores. The organic chromophore dye molecules, assembled onto the surface of the mesopores, would have the amino groups exposed to the surface. These groups would have the capability to selectively interact with ions or chemical compounds in solution, for instance lead ions in water. Hence, the absorption spectrum of the chromophore dye molecules attached to the mesopores of silica was altered after exposure to lead ions in solution. In addition, the ion concentration in solution also differed. Such functionalized, hierarchically-structured mesoporous silica would have applications such as membranes for removal of, and sensors for, detecting trace amounts of ions and chemical compounds in water and air.
Cadmium Tungstate is a complex oxide which gains considerable attention as a scintillator material. The material has high radiation hardness and in crystalline form is highly efficient. It is also non-hydroscopic, unlike the more efficient thallium doped NaI crystal. A processing technique utilizing sol gel technology has been successfully applied to this system for the first time to allow for more precise stoichiometry control, as well as to produce thin films more easily and cheaply than other methods. The as-produced material consists of single phase, stoichiometric nano-crystallites of cadmium tungstate and shows photoluminescence at 480nm. The material was characterized by X-ray diffraction, SEM and PL analysis.
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