On Hydrogen Fugacity in Metals Under Electrolytic Charging

Author(s):  
Yu. S. Nechaev
Keyword(s):  
2008 ◽  
Author(s):  
A. C. Simon ◽  
Kazuyuki Tohji ◽  
Noriyoshi Tsuchiya ◽  
Balachandran Jeyadevan

1986 ◽  
Vol 20 (5) ◽  
pp. 653-658 ◽  
Author(s):  
G.M Bond ◽  
I.M Robertson ◽  
H.K Birnbaum

CORROSION ◽  
1980 ◽  
Vol 36 (10) ◽  
pp. 544-549 ◽  
Author(s):  
D. F. TAYLOR ◽  
M. SILVERMAN

Abstract Crevice experiments with 1 mm ID Alloy 600, 304L stainless steel, and platinum tubing have shown that to a large extent, equilibrium thermodynamics controls the mode and degree of crevice corrosion in aqueous systems at 288 C. When crevices enter a potential/pH region of thermodynamic instability for the crevice solution, direct reduction of water or hydrogen ions by the metal competes with macrocell acidification and the hydrogen fugacity strongly influences the degree of acidity which can be attained or maintained. The platinum system undergoes no such thermodynamic transition and acidification ceases only as the corrosion macrocell approaches equilibrium. Platinum crevice behavior indicates an upper limit of 0.60 V (SHE) for the Pt(II) oxide/Pt standard potential at 288 C.


Author(s):  
H. Z. Xiao ◽  
I. M. Robertson ◽  
H. K. Birnbaum

The intermetallic compound Ti3Al (DO19’, an ordered hexagonal structure) has, because of its high strength to weight ratio, stimulated extensive studies. As a consequence of the improved ductility through the addition of niobium, Ti3Al can be considered for use at both high and low temperatures. Since many applications for this material also involve high hydrogen fugacity environment, the mechanism of hydrogen embrittlement (related to the hydride formation) must be understood. In the present study of the interaction of Ti3Al with gaseous hydrogen we have applied the methods of TEM, electron diffraction, X-ray scattering and gas chromatographic H analysis. Specimens of Ti3Al were equilibrated with gaseous H2 at a pressure of 700 torr at temperatures of 373 K and 323 K for two and seven days, respectively. This resulted in H/metal values of 0.59 and 1.67, respectively. The specimens fractured severely during the gaseous charging and were subsequently ground into fine powders under pure ethyl alcohol. These powders were used for the TEM studies. TEM examinations were performed at 120 kV using a Philips 420 electron microscope.


2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Shunsuke Hashimoto ◽  
Takaaki Tsuda ◽  
Kyohei Ogata ◽  
Takeshi Sugahara ◽  
Yoshiro Inoue ◽  
...  

Thermodynamic stability and hydrogen occupancy on the hydrogen + tetra-n-butyl ammonium bromide semi-clathrate hydrate were investigated by means of Raman spectroscopic and phase equilibrium measurements under the three-phase equilibrium condition. The structure of mixed gas hydrates changes from tetragonal to another structure around 95 MPa and 292 K depending on surrounding hydrogen fugacity. The occupied amount of hydrogen in the semi-clathrate hydrate increases significantly associated with the structural transition. Tetra-n-butyl ammonium bromide semi-clathrate hydrates can absorb hydrogen molecules by a pressure-swing without destroying the hydrogen bonds of hydrate cages at 15 MPa or over.


2017 ◽  
Vol 127 ◽  
pp. 45-58 ◽  
Author(s):  
Jeffrey Venezuela ◽  
Evan Gray ◽  
Qinglong Liu ◽  
Qingjun Zhou ◽  
Clotario Tapia-Bastidas ◽  
...  

Minerals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 712
Author(s):  
Sokol ◽  
Sokol ◽  
Bul’bak ◽  
Nefyodov ◽  
Zaikin ◽  
...  

C- and N-bearing species in reduced fluids weree studied experimentally in C–O–H–N and muscovite–C–O–H–N systems and in natural carbonate-bearing samples at mantle P–T parameters. The experiments reproduced three types of reactions leading to formation of hydrocarbons (HCs) at 3.8–7.8 GPa and 800–1400 C and at hydrogen fugacity (fH2) buffered by the Fe–FeO (IW) + H2O or Mo–MoO2 (MMO) + H2O equilibria: (i) Thermal destruction of organic matter during its subduction into the mantle (with an example of docosane), (ii) hydrogenation of graphite upon interaction with H2‑enriched fluids, and (iii) hydrogenation of carbonates and products of their reduction in metamorphic clayey rocks. The obtained quenched fluids analyzed after the runs by gas chromatography-mass spectrometry (GC–MS) and electronic ionization mass-spectrometry (HR–MS) contain CH4 and C2H6 as main carbon species. The concentrations of C2-C4 alkanes in the fluids increase as the pressure and temperature increase from 3.8 to 7.8 GPa and from 800 to 1400 C, respectively. The fluid equilibrated with the muscovite–garnet–omphacite–kyanite–rutile ± coesite assemblage consists of 50–80 rel.% H2O and 15–40 rel.% alkanes (C1 > C2 > C3 > C4). Main N-bearing species are ammonia (NH3) in the C–O–H–N and muscovite–C–O–H–N systems or methanimine (CH3N) in the fluid derived from the samples of natural pelitic rocks. Nitrogen comes either from air or melamine (C3H6N6) in model systems or from NH4+ in the runs with natural samples. The formula CH3N in the quenched fluid of the C–O–H–N system is confirmed by HR–MS. The impossibility of CH3N incorporation into K-bearing silicates because of a big CH3NH+ cation may limit the solubility of N in silicates at low fO2 and hence may substantially influence the mantle cycle of nitrogen. Thus, subduction of slabs containing carbonates, organic matter, and N-bearing minerals into strongly reduced mantle may induce the formation of fluids enriched in H2O, light alkanes, NH3, and CH3N. The presence of these species must be critical for the deep cycles of carbon, nitrogen, and hydrogen.


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