Nuclear relaxation at high temperature in the one-dimensional Heisenberg system CuNSal

1977 ◽  
Vol 23 (9) ◽  
pp. 673-677 ◽  
Author(s):  
C. Jeandey ◽  
J.P. Boucher ◽  
F. Ferrieu ◽  
M. Nechtschein
1974 ◽  
Vol 15 (1) ◽  
pp. 25-28 ◽  
Author(s):  
M. Ahmed-Bakheit ◽  
Y. Barjhoux ◽  
F. Ferrieu ◽  
M. Nechtschein ◽  
J-P. Boucher

Author(s):  
M. G. McKellar ◽  
J. E. O’Brien ◽  
C. M. Stoots ◽  
G. L. Hawkes

A process model has been developed to evaluate the potential performance of a large-scale high-temperature co-electrolysis plant for the production of syngas from steam and carbon dioxide. The co-electrolysis process allows for direct electrochemical reduction of the steam-carbon dioxide gas mixture, yielding hydrogen and carbon monoxide, or syngas. The process model has been developed using the Honeywell UniSim systems analysis code. Using this code, a detailed process flow sheet has been defined that includes all the components that would be present in an actual plant such as pumps, compressors, heat exchangers, turbines, and the electrolyzer. Since the electrolyzer is not a standard UniSim component, a custom one-dimensional co-electrolysis model was developed for incorporation into the overall UniSim process flow sheet. The one dimensional co-electrolysis model assumes local chemical equilibrium among the four process-gas species via the gas shift reaction. The electrolyzer model allows for the determination of co-electrolysis outlet temperature, composition (anode and cathode sides); mean Nernst potential, operating voltage and electrolyzer power based on specified inlet gas flow rates, heat loss or gain, current density, and cell area-specific resistance. The one-dimensional electrolyzer model was validated by comparison with results obtained from a fully three dimensional computational fluid dynamics model developed using FLUENT, and by comparison to experimental data. This paper provides representative results obtained from the UniSim flow sheet model for a 300 MW co-electrolysis plant, coupled to a high-temperature gas-cooled nuclear reactor. The co-electrolysis process, coupled to a nuclear reactor, provides a means of recycling carbon dioxide back into a useful liquid fuel. If the carbon dioxide source is based on biomass, the entire process would be climate neutral.


2001 ◽  
Vol 64 (19) ◽  
Author(s):  
I. C. Charret ◽  
E. V. Corrêa Silva ◽  
S. M. de Souza ◽  
O. Rojas Santos ◽  
M. T. Thomaz ◽  
...  

Author(s):  
J. E. O’Brien ◽  
C. M. Stoots ◽  
J. Stephen Herring ◽  
G. L. Hawkes

A one-dimensional model has been developed to predict the thermal and electrochemical behavior of a high-temperature steam electrolysis stack. This electrolyzer model allows for the determination of the average Nernst potential, cell operating voltage, gas outlet temperatures, and electrolyzer efficiency for any specified inlet gas flow rates, current density, cell active area, and external heat loss or gain. The model includes a temperature-dependent area-specific resistance (ASR) that accounts for the significant increase in electrolyte ionic conductivity that occurs with increasing temperature. Model predictions are shown to compare favorably with results obtained from a fully 3-D computational fluid dynamics model. The one-dimensional model was also employed to demonstrate the expected trends in electrolyzer performance over a range of operating conditions including isothermal, adiabatic, constant steam utilization, constant flow rate, and the effects of operating temperature.


1976 ◽  
Vol 13 (9) ◽  
pp. 4098-4118 ◽  
Author(s):  
J. P. Boucher ◽  
M. Ahmed Bakheit ◽  
M. Nechtschein ◽  
M. Villa ◽  
G. Bonera ◽  
...  

2010 ◽  
Vol 43 (5) ◽  
pp. 1062-1067 ◽  
Author(s):  
Rupesh S. Devan ◽  
Jin-Han Lin ◽  
Wei-Der Ho ◽  
Sheng Yun Wu ◽  
Yung Liou ◽  
...  

The thermochromic phase transformations that occur in one-dimensional Ta2O5nanorods were analysed at elevated temperatures ranging from 300 to 750 K. X-ray photoemission spectroscopy data revealed not only the electronic structures and chemical properties of the one-dimensional Ta2O5nanorods, but also their stoichiometric Ta and O compositions. High-temperature X-ray diffraction data revealed complex and polymorphic thermochromic phase transformations of the α(1 0 11), α(200), α(2 0 10), β(3 11 1) and β(2 21 1) lattice planes in the one-dimensional Ta2O5nanorods, which incorporate β to α (β–α), β to β (β–β), α to α (α–α) and α to β (α–β) phase transitions. The thermochromic phase transformations between α- and β-phase crystals can be explained by a shift in 2θ and expansion of thedspacing of the lattice planes.


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