The rate of hydrogen evolution on Beta III titanium alloy in 1.0, 2.5, 5.0, 7.5, and 10.0 N sulfuric acid at 23, 45, 60, and 75 C (73, 113, 140, and 167 F) has been investigated. The cathodic Tafel slopes were 60, 64, 67, and 70 mV, respectively, at each temperature. The reaction order was first order with respect to the concentration of hydrogen ions. The chemical recombination mechanism for the hydrogen evolution reaction using the Temkin adsorption isotherm with activated heat of adsorption is consistent with the experimental data. The corrosion rate increased with increase in both acid concentration and temperature. The activation energies for corrosion were 22.1, 20.8, and 19.3 kcal/mole for corrosion in 1.0, 2.5, and 5.0 N H2SO4, respectively, and 15.9 kcal/mole in 7.5 and 10.0 N H2SO4.
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1 August 1974
Research Article|
August 01 1974
Hydrogen Evolution on Beta III Titanium Alloy Available to Purchase
Dennis L. Dull;
Dennis L. Dull
*Aerospace Corporation, El Segundo, California.
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Ken Nobe
Ken Nobe
**School of Engineering and Applied Science, University of California, Los Angeles, CA 90024.
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Received:
September 01 1973
Online ISSN: 1938-159X
Print ISSN: 0010-9312
© 1974 National Association of Corrosion Engineers
1974
CORROSION (1974) 30 (8): 291–295.
Article history
Received:
September 01 1973
Citation
Dennis L. Dull, Ken Nobe; Hydrogen Evolution on Beta III Titanium Alloy. CORROSION 1 August 1974; 30 (8): 291–295. https://doi.org/10.5006/0010-9312-30.8.291
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