Publications

Krumhansl, James L.; Garino, Terry J.; Rademacher, David R.

Abstract not provided.

Garino, Terry J.; Krumhansl, James L.

Abstract not provided.

Tuttle, Bruce T.; Sipola, Diana L.; Garino, Terry J.; Mahoney, Patrick M.; Rodriguez, Marko A.; Voigt, James A.

Fine powders of calcium zirconate (CaZrO{sub 3}, CZ) and calcium titanate (CaTiO{sub 3}, CT) were synthesized using a nonaqueous oxalate co-precipitation route from Ca(NO{sub 3}){sub 2}{center_dot}4 H{sub 2}O and group(IV) n-butoxides (Ti(OBu{sup n}){sub 4} or Zr(OBu{sup n}){sub 4}). Several reaction conditions and batch sizes (2-35 g) were explored to determine their influence on final particle size, morphology, and phase. Characterization of the as-prepared oxalate precursors, oven dried oxalate precursors (60-90 C), and calcined powders (635-900 C) were analyzed with TGA/DTA, XRD, TEM, and SEM. Densification and sintering studies on pressed CZ pellets at 1375 and 1400 C were also performed. Through the developed oxalate co-precipitation route, densification temperatures for CZ were lowered by 125 C from the 1500 C firing temperature required for conventional mixed oxide powders. Low field electrical tests of the CZ pellets indicated excellent dielectric properties with dielectric constants of {approx}30 and a dissipation factor of 0.0004 were measured at 1 kHz.

Garino, Terry J.; Tandon, Rajan T.

Glasses filled with ceramic or metallic powders have been developed for use as seals for solid oxide fuel cells (SOFC's) as part of the U.S. Department of Energy's Solid State Energy Conversion Alliance (SECA) Program. The composites of glass (alkaline earth-alumina-borate) and powders ({approx}20 vol% of yttria-stabilized zirconia or silver) were shown to form seals with SOFC materials at or below 900 C. The type and amount of powder were adjusted to optimize thermal expansion to match the SOFC materials and viscosity. Wetting studies indicated good wetting was achieved on the micro-scale and reaction studies indicated that the degree of reaction between the filled glasses and SOFC materials, including spinel-coated 441 stainless steel, at 750 C is acceptable. A test rig was developed for measuring strengths of seals cycled between room temperature and typical SOFC operating temperatures. Our measurements showed that many of the 410 SS to 410 SS seals, made using silver-filled glass composites, were hermetic at 0.2 MPa (2 atm.) of pressure and that seals that leaked could be resealed by briefly heating them to 900 C. Seal strength measurements at elevated temperature (up to 950 C), measured using a second apparatus that we developed, indicated that seals maintained 0.02 MPa (0.2 atm.) overpressures for 30 min at 750 C with no leakage. Finally, the volatility of the borate component of sealing glasses under SOFC operational conditions was studied using weight loss measurements and found by extrapolation to be less than 5% for the projected SOFC lifetime.

Garino, Terry J.; Nenoff, T.M.; Krumhansl, James L.; Ockwig, Nathan O.

Abstract not provided.

Garino, Terry J.; Siegel, Nathan P.

Abstract not provided.

Garino, Terry J.; Siegel, Nathan P.

Abstract not provided.

Garino, Terry J.; Voigt, James A.; Spoerke, Erik D.; Sipola, Diana L.; Lockwood, Steven J.; Yang, Pin Y.; Gibson, Julie T.

Abstract not provided.

Garino, Terry J.; Rodriguez, Marko A.

Abstract not provided.

Garino, Terry J.; Rodriguez, Marko A.

The sintering behavior of Sandia chem-prep high field varistor materials was studied using techniques including in situ shrinkage measurements, optical and scanning electron microscopy and x-ray diffraction. A thorough literature review of phase behavior, sintering and microstructure in Bi{sub 2}O{sub 3}-ZnO varistor systems is included. The effects of Bi{sub 2}O{sub 3} content (from 0.25 to 0.56 mol%) and of sodium doping level (0 to 600 ppm) on the isothermal densification kinetics was determined between 650 and 825 C. At {ge} 750 C samples with {ge}0.41 mol% Bi{sub 2}O{sub 3} have very similar densification kinetics, whereas samples with {le}0.33 mol% begin to densify only after a period of hours at low temperatures. The effect of the sodium content was greatest at {approx}700 C for standard 0.56 mol% Bi{sub 2}O{sub 3} and was greater in samples with 0.30 mol% Bi{sub 2}O{sub 3} than for those with 0.56 mol%. Sintering experiments on samples of differing size and shape found that densification decreases and mass loss increases with increasing surface area to volume ratio. However, these two effects have different causes: the enhancement in densification as samples increase in size appears to be caused by a low oxygen internal atmosphere that develops whereas the mass loss is due to the evaporation of bismuth oxide. In situ XRD experiments showed that the bismuth is initially present as an oxycarbonate that transforms to metastable {beta}-Bi{sub 2}O{sub 3} by 400 C. At {approx}650 C, coincident with the onset of densification, the cubic binary phase, Bi{sub 38}ZnO{sub 58} forms and remains stable to >800 C, indicating that a eutectic liquid does not form during normal varistor sintering ({approx}730 C). Finally, the formation and morphology of bismuth oxide phase regions that form on the varistors surfaces during slow cooling were studied.

Tuttle, Bruce T.; Williams, David P.; Garino, Terry J.; Sipola, Diana L.; Voigt, James A.

Abstract not provided.

Garino, Terry J.; Yang, Pin Y.; Voigt, James A.; Lockwood, Steven J.; Sipola, Diana L.

Abstract not provided.

Ambrosini, Andrea A.; Nenoff, T.M.; Garino, Terry J.

Abstract not provided.

Ambrosini, Andrea A.; Gelbard, Fred G.; Garino, Terry J.; Leung, Kevin L.

In an effort to produce hydrogen without the unwanted greenhouse gas byproducts, high-temperature thermochemical cycles driven by heat from solar energy or next-generation nuclear power plants are being explored. The process being developed is the thermochemical production of Hydrogen. The Sulfur-Iodide (SI) cycle was deemed to be one of the most promising cycles to explore. The first step of the SI cycle involves the decomposition of H{sub 2}SO{sub 4} into O{sub 2}, SO{sub 2}, and H{sub 2}O at temperatures around 850 C. In-situ removal of O{sub 2} from this reaction pushes the equilibrium towards dissociation, thus increasing the overall efficiency of the decomposition reaction. A membrane is required for this oxygen separation step that is capable of withstanding the high temperatures and corrosive conditions inherent in this process. Mixed ionic-electronic perovskites and perovskite-related structures are potential materials for oxygen separation membranes owing to their robustness, ability to form dense ceramics, capacity to stabilize oxygen nonstoichiometry, and mixed ionic/electronic conductivity. Two oxide families with promising results were studied: the double-substituted perovskite A{sub x}Sr{sub 1-x}Co{sub 1-y}B{sub y}O{sub 3-{delta}} (A=La, Y; B=Cr-Ni), in particular the family La{sub x}Sr{sub 1-x}Co{sub 1-y}Mn{sub y}O{sub 3-{delta}} (LSCM), and doped La{sub 2}Ni{sub 1-x}M{sub x}O{sub 4} (M = Cu, Zn). Materials and membranes were synthesized by solid state methods and characterized by X-ray and neutron diffraction, SEM, thermal analyses, calorimetry and conductivity. Furthermore, we were able to leverage our program with a DOE/NE sponsored H{sub 2}SO{sub 4} decomposition reactor study (at Sandia), in which our membranes were tested in the actual H{sub 2}SO{sub 4} decomposition step.

Garino, Terry J.

This proposal focuses on the synthesis and characterization of ''tunable'' perovskite ceramics with resulting controlled strength and temperature of dielectric constants and/or with ionic conductivity. Traditional methods of synthesis involve high temperature oxide mixing and baking. We developed a new methodology of synthesis involving the (1) low temperature hydrothermal synthesis of metastable porous phases with ''tuned'' stoichiometry, and element types, and then (2) low temperature heat treatment to build exact stoichiometry perovskites, with the desired vacancy concentrations. This flexible pathway can lead to compositions and structures not attainable by conventional methods. During the course of this program, a series of Na-Nb perovskites were synthesized by calcining and collapsing microporous Sandia Octahedral Molecular Sieve (SOMS) phases. These materials were studied by various characterization techniques and conductivity measurements to better delineate stability and stoichiometry/bulk conductivity relationships. The conductivity can be altered by changing the concentration and type of the substituting framework cation(s) or by ion exchange of sodium. To date, the Na{sub 0.9}Mg{sub 0.1}Nb{sub 0.8}Ti{sub 0.2}O{sub 3-{delta}} shows the best conductivity.

Garino, Terry J.; Phifer, Carol P.; Voigt, James A.; Sipola, Diana L.

Abstract not provided.

Williams, David P.; Tuttle, Bruce T.; Voigt, James A.; Sipola, Diana L.; Niehaus, Michael K.; Cesarano, Joseph C.; Garino, Terry J.

Abstract not provided.

Ewsuk, Kevin G.; Arguello, Jose G.; Garino, Terry J.

Abstract not provided.

Garino, Terry J.; Phifer, Carol P.; Voigt, James A.; Sipola, Diana L.

Abstract not provided.

Ewsuk, Kevin G.; Arguello, Jose G.; Garino, Terry J.

Abstract not provided.

Garino, Terry J.; Arguello, Jose G.

Abstract not provided.

Nenoff, T.M.; Garino, Terry J.

Materials in the La{sub 0.1}Sr{sub 0.9}Co{sub 1-y}MnyO{sub 3-{delta}} (LSCM) family are potentially useful as ceramic membranes for high-temperature oxygen separations. A series of LSCM samples was synthesized by solid state methods and characterized by powder X-ray diffraction, thermogravimetric analysis, and four-probe conductivity. The materials were indexed in the cubic Pm-3m space group. TGA data implied that LSCM can reversibly absorb and desorb oxygen versus temperature and partial oxygen pressure, while powder diffraction data showed that the material maintained the cubic perovskite structure. Preliminary four-probe conductivity measurements signify p-type semiconducting behavior.

Morales, Alfredo M.; Garino, Terry J.

Abstract not provided.

Glass, Sarah J.; Ewsuk, Kevin G.; Garino, Terry J.; Arguello, Jose G.; Reiterer, Markus W.

Abstract not provided.

Reiterer, Markus W.; Garino, Terry J.; Uribe, Fernando U.

Abstract not provided.