Open AccessThermodynamic behavior of dissolved oxygen and hydrogen in pure vanadium
Author(s) -
Dapeng Zhong,
Guishang Pei,
Junyi Xiang,
Chuyu Pan,
Wenling Gu,
Xuewei Lv
Publication year - 2021
Publication title -
journal of mining and metallurgy. section b, metallurgy/journal of mining and metallurgy. section b, metallurgy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.42
H-Index - 20
eISSN - 2217-7175
pISSN - 1450-5339
DOI - 10.2298/jmmb210108037z
Subject(s) - vanadium , deoxygenation , gibbs free energy , oxygen , metal , chemistry , hydrogen , reducing agent , thermodynamic equilibrium , inorganic chemistry , thermodynamics , catalysis , organic chemistry , physics
The mechanism governing the deoxidation of vanadium metal is regarded as fundamental knowledge; however, it has not been elucidated in existing literature. In this paper, the thermodynamic data of V-H-O systems were summarized, and the Gibbs free energies of the main compounds were calculated. Consequently, the deoxidation limits of different reductants in a V-O system were evaluated, namely: Si, Al, and Mg. It was observed that Si cannot remove an O content of less than 7.27 wt% from V. However, Al was the stronger reducing agent; it could remove O contents of up to 0.01 and 0.1 wt% at 800 and 1050 ?C, respectively. Nevertheless, Mg exhibited the best reducing properties as it could remove less than 0.01 wt% of O at 1100 ?C. The addition of H2 renders the V-O solid solution unstable to a certain extent, thereby indicating that H2 facilitates deoxygenation. Furthermore, the results obtained by analyzing the equilibrium conditions were in accordance with the results of the deoxidation limit in the V-O system. In other words, this study demonstrates that the oxygen in vanadium can be effectively controlled by changing the reductant dosage and temperature.