Steps and kinks on {211} iron surfaces and the kinetics of the iron electrode

1979 ◽  
Vol 9 (2) ◽  
pp. 155-160 ◽  
Author(s):  
W. Allgaier ◽  
K. E. Heusler
Keyword(s):  
Iron Electrode ◽  
Kinetics Of

Kinetics of electrode processes on the iron electrode

1947 ◽  
Vol 1 ◽  
pp. 259 ◽  
Author(s):  
B. Kabanov ◽  
R. Burstein ◽  
A. Frumkin
Keyword(s):  
Iron Electrode ◽  
Electrode Processes ◽  
Kinetics Of

Kinetics of Carbon Tetrachloride Reduction at an Oxide-Free Iron Electrode

1997 ◽  
Vol 31 (8) ◽  
pp. 2385-2391 ◽  
Author(s):  
Michelle M. Scherer ◽  
John C. Westall ◽  
Margaret Ziomek-Moroz ◽  
Paul G. Tratnyek
Keyword(s):  
Carbon Tetrachloride ◽  
Iron Electrode ◽  
Free Iron ◽  
Kinetics Of

Studies of the kinetics of aluminium incorporation into an iron electrode in molten salts by linear sweep voltammetry

1989 ◽  
Vol 19 (2) ◽  
pp. 271-274 ◽  
Author(s):  
F. Lantelme ◽  
E. Cherrat ◽  
Y. Chryssoulakis ◽  
S. Kalogeropoulou
Keyword(s):  
Molten Salts ◽  
Linear Sweep Voltammetry ◽  
Iron Electrode ◽  
Linear Sweep ◽  
Kinetics Of

The Hydrogen Evolution Reaction on Fe Electrode Material in 1 M NaOH Solution

2015 ◽  
Vol 228 ◽  
pp. 252-257 ◽  
Author(s):  
Magdalena Popczyk ◽  
B. Łosiewicz
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Electrode Material ◽  
Electrochemical Impedance ◽  
Porous Electrodes ◽  
Iron Electrode ◽  
Iron Corrosion ◽  
Naoh Solution ◽  
Eis Measurements ◽  
Kinetics Of

Kinetics of hydrogen evolution reaction (HER) was investigated in 1 M NaOH solution at room temperature on a polycrystalline Fe electrode material which was electrochemically activated and unactivated. Studies of the HER were carried out using steady-state polarization and electrochemical impedance spectroscopy (EIS) measurements. It was found that for the Fe electrode material after activation atj= -320 mA cm-2for 24 h, the increase in the catalytic activity towards the HER was observed in comparison with that on the unactivated iron electrode material.Acimpedance behavior of the Fe electrode changed from a typical for smooth electrodes before activation (one time constant in the circuit) to that being characteristic for porous electrodes after activation (two time constants in the circuit). The reason for that is formation of solid products of the iron corrosion in alkaline solution which can cause passivation of the electrode surface and catalyse the HER.

Direct observations of radiation-enhanced transformations in glass

1983 ◽  
Vol 41 ◽  
pp. 354-355
Author(s):  
J. F. DeNatale ◽  
D. G. Howitt
Keyword(s):  
Glass Matrix ◽  
Diffusion Mechanism ◽  
Bubble Formation ◽  
Silicate Glasses ◽  
Phase Decomposition ◽  
Direct Observations ◽  
Thin Foils ◽  
Oxygen Bubble ◽  
Electron Energy Loss ◽  
Kinetics Of

The electron irradiation of silicate glasses containing metal cations produces various types of phase separation and decomposition which includes oxygen bubble formation at intermediate temperatures figure I. The kinetics of bubble formation are too rapid to be accounted for by oxygen diffusion but the behavior is consistent with a cation diffusion mechanism if the amount of oxygen in the bubble is not significantly different from that in the same volume of silicate glass. The formation of oxygen bubbles is often accompanied by precipitation of crystalline phases and/or amorphous phase decomposition in the regions between the bubbles and the detection of differences in oxygen concentration between the bubble and matrix by electron energy loss spectroscopy cannot be discerned (figure 2) even when the bubble occupies the majority of the foil depth.The oxygen bubbles are stable, even in the thin foils, months after irradiation and if van der Waals behavior of the interior gas is assumed an oxygen pressure of about 4000 atmospheres must be sustained for a 100 bubble if the surface tension with the glass matrix is to balance against it at intermediate temperatures.

Irradiation behavior of pyrolytic silicon carbide

1983 ◽  
Vol 41 ◽  
pp. 72-73
Author(s):  
R. J. Lauf
Keyword(s):  
Silicon Carbide ◽  
Fission Products ◽  
Thermodynamics And Kinetics ◽  
Neutron Fluences ◽  
Fuel Particles ◽  
Sic Coatings ◽  
Irradiation Behavior ◽  
Kinetics Of ◽  
Htgr Fuel

Fuel particles for the High-Temperature Gas-Cooled Reactor (HTGR) contain a layer of pyrolytic silicon carbide to act as a miniature pressure vessel and primary fission product barrier. Optimization of the SiC with respect to fuel performance involves four areas of study: (a) characterization of as-deposited SiC coatings; (b) thermodynamics and kinetics of chemical reactions between SiC and fission products; (c) irradiation behavior of SiC in the absence of fission products; and (d) combined effects of irradiation and fission products. This paper reports the behavior of SiC deposited on inert microspheres and irradiated to fast neutron fluences typical of HTGR fuel at end-of-life.

The Ordered Phase Formation in Ti-Al-Ga Alloys

1970 ◽  
Vol 28 ◽  
pp. 440-441
Author(s):  
Shiro Fujishiro ◽  
Harold L. Gegel
Keyword(s):  
Thermal Stability ◽  
High Temperature ◽  
Titanium Alloys ◽  
Growth Kinetics ◽  
Stoichiometric Composition ◽  
Good Potential ◽  
Alpha Titanium ◽  
Cold Rolled ◽  
Kinetics Of ◽  
Thermal Stability Of

Ordered-alpha titanium alloys having a DO19 type structure have good potential for high temperature (600°C) applications, due to the thermal stability of the ordered phase and the inherent resistance to recrystallization of these alloys. Five different Ti-Al-Ga alloys consisting of equal atomic percents of aluminum and gallium solute additions up to the stoichiometric composition, Ti3(Al, Ga), were used to study the growth kinetics of the ordered phase and the nature of its interface.The alloys were homogenized in the beta region in a vacuum of about 5×10-7 torr, furnace cooled; reheated in air to 50°C below the alpha transus for hot working. The alloys were subsequently acid cleaned, annealed in vacuo, and cold rolled to about. 050 inch prior to additional homogenization

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