다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

II. Structure of Perovskites 1982 A. Crystal Structure 1982 B. Nonstoichiometry in Perovskites 1983 1. Oxygen Nonstoichiometry 1983 2. Cation Nonstoichiometry 1984 C. Physical Properties 1985 D. Adsorption Properties 1986 1. CO and NO Adsorption 1986 2. Oxygen Adsorption 1987 E. Specific Surface and Porosity 1987 F. Thermal Stability in a Reducing Atmosphere 1989 III. Acid−Base and Redox Properties 1990 A. Acidity and Basicity 1990 B. Redox Processes 1991 1. Kinetics and Mechanisms 1992 2. Reduction−Oxidation Cycles 1993 C. Ion Mobility 1993 1. Oxygen Transport 1993 2. Cation Transport 1994 IV. Heterogeneous Catalysis 1995 A. Oxidation Reactions 1995 1. CO Oxidation 1995 2. Oxidation of Hydrocarbons 1996 B. Pollution Abatement 2001 1. NOx Decomposition 2001 2. Exhaust Treatment 2002 3. Stability 2004 C. Hydrogenation and Hydrogenolysis Reactions 2004 1. Hydrogenation of Carbon Oxides 2004 2. Hydrogenation and Hydrogenolysis Reactions 2006

Chemical structures and performance of perovskite oxides.

Recent worldwide interest in building a decentralized, hydrogen-based energy economy has refocused attention on the solid oxide fuel cell (SOFC) as a potential source of efficient, environmentally friendly, fuel-versatile electric power. Due to its high operating temperature, the SOFC offers several potential advantages over polymer-based fuel cells, including reversible electrode reactions, low internal resistance, high tolerance to typical catalyst poisons, production of high-quality waste heat for (among other uses) reformation of hydrocarbon fuels, as well as the possibility of burning hydrocarbon fuels directly. Today, SOFCs are much closer to commercial reality than they were 20 years ago, due largely to technological advances in electrode material composition, microstructure control, thin-film ceramic fabrication, and stack and system design. These advances have led to dozens of active SOFC development programs in both stationary and mobile power and contributed to commercialization or development in a number of related technologies, including gas sensors,1 solid-state electrolysis devices,2 and iontransport membranes for gas separation and partial oxidation.3 Many reviews are available which summarize the technological advances made in SOFCs over the last 15-35 yearssreaders who are primarily interested in knowing the state-of-the art in materials, design, and fabrication (including the electrodes) are encouraged to consult these reviews.4-12 This review focuses on the factors governing SOFC cathode performancesadvances we have made over † Dedicated to Brian Steele, 1929-2003. Researcher, Entrepreneur, Consensus Seeker. 4791 Chem. Rev. 2004, 104, 4791−4843

Factors Governing Oxygen Reduction in Solid Oxide Fuel Cell Cathodes

Solid oxide fuel cells (SOFCs) have the promise to improve energy efficiency and to provide society with a clean energy producing technology. The high temperature of operation (500−1000 °C) enables the solid oxide fuel cell to operate with existing fossil fuels and to be efficiently coupled with turbines to give very high efficiency conversion of fuels to electricity. Solid oxide fuel cells are complex electrochemical devices that contain three basic components, a porous anode, an electrolyte membrane, and a porous cathode. In this short review, a survey of the types and properties of materials that have been considered for each of these components is presented with an emphasis on the requirements for operation at intermediate temperature (500−800 °C). Some directions for future research are discussed.

Materials for Solid Oxide Fuel Cells

Progress in material selection for solid oxide fuel cell technology: A review

https://ris.utwente.nl/ws/files/6511980/Bouwmeester94importance.pdf

Importance of the surface exchange kinetics as rate limiting step in oxygen permeation through mixed-conducting oxides

The structure, oxygen stoichiometry, and chemical and thermal expansion of Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) between 873 and 1173 K and oxygen partial pressures of 1 × 10-3 to 1 atm were determined by in situ neutron diffraction. BSCF has a cubic perovskite structure, space group Pm3m, across the whole T−pO2 region investigated. The material is highly oxygen deficient with a maximum oxygen stoichiometry (3 − δ) of 2.339(12) at 873 K and a pO2 of 1 atm and a minimum of 2.192(15) at 1173 K and a pO2 of 10-3 atm. Good agreement is obtained between oxygen stoichiometry data determined by neutron diffraction and thermogravimetry. In the range covered by the experiments, the thermal and chemical expansion coefficients are 19.0(5)−20.8(6) × 10-6 K-1 and 0.016(2)−0.026(4), respectively.

Oxygen stoichiometry and chemical expansion of Ba0.5Sr0.5Co0.8Fe0.2O3- δ measured by in situ neutron diffraction

https://ris.utwente.nl/ws/files/6795625/Kruidhof93influence.pdf

Influence of order-disorder transitions on oxygen permeability through selected nonstoichiometric perovskite-type oxides

Ionic-electronic mixed-conducting perovskite-type oxide La0.6Sr0.4Co0.8Fe0.2O3 was applied as a dense membrane for oxygen supply in a reactor for methane coupling. The oxygen permeation properties were studied in the pO2-range of 10?3?1 bar at 1073?1273 K, using helium as a sweeping gas at the permeate side of the membrane. The oxygen semi-permeability has a value close to 1 mmol m?2 s?1 at 1173 K with a corresponding activation energy of 130?140 kJ/mol. The oxygen flux is limited by a surface process at the permeate side of the membrane. It was found that the oxygen flux is only slightly enhanced if methane is admixed with helium. Methane is converted to ethane and ethene with selectivities up to 70%, albeit that conversions are low, typically 1?3% at 1073?1173 K. When oxygen was admixed with methane rather than supplied through the membrane, selectivities obtained were found to be in the range 30?35%. Segregation of strontium was found at both sides of the membrane, being seriously affected by the presence of an oxygen pressure gradient across it. The importance of a surface limited oxygen flux for application of perovskite membranes for methane coupling is emphasized.

/pdf/oxidative-coupling-of-methane-in-a-mixed-conducting-1t7q3yv2ak.pdf

Oxidative coupling of methane in a mixed-conducting perovskite membrane reactor

Electrical conductivity relaxation experiments were performed on thin specimens of La1–xSrxFeO3–delta (x = 0.1, 0.4) at oxygen partial pressures pO2 = 10–5 – 1 bar in the temperature range 923 to 1223 K. The transient response of the electrical conductivity after a sudden change of the ambient oxygen partial pressure was analyzed in the frequency domain. The latter procedure allowed diffusion-limited and surface exchange-limited kinetics of re-equilibration to be distinguished. The response of specimens with thicknesses of 350 to 460 µm indicated diffusion-controlled kinetics at pO2 > 0.03 bar. The chemical diffusion coefficients, D-tilde , were found invariant with oxygen pressure. At 1073 K the absolute values were D-tilde = 6.5 × 10–6 cm2 s–1 for x = 0.1 and D-tilde = 1.1 × 10–5 cm2 s–1 for x = 0.4, with activation energies of about 80 kJ/mol. The equilibration process was governed by surface exchange at pO2 O[sub 2] n , where n = 0.65 to 0.85. This pressure dependency was interpreted in terms of a slow surface process involving an oxygen molecule and a surface oxygen vacancy, and causes the observed sharp transition from diffusion- to exchange-controlled kinetics. The activation energy of kO was estimated at 110 to 135 kJ/mol.

/pdf/oxygen-exchange-and-diffusion-coefficients-of-strontium-2ctf90ujc6.pdf

Henny J.M. Bouwmeester

Papers

Importance of the surface exchange kinetics as rate limiting step in oxygen permeation through mixed-conducting oxides

Oxygen stoichiometry and chemical expansion of Ba0.5Sr0.5Co0.8Fe0.2O3- δ measured by in situ neutron diffraction

Influence of order-disorder transitions on oxygen permeability through selected nonstoichiometric perovskite-type oxides

Oxidative coupling of methane in a mixed-conducting perovskite membrane reactor

Oxygen Exchange and Diffusion Coefficients of Strontium‐Doped Lanthanum Ferrites by Electrical Conductivity Relaxation