% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@PHDTHESIS{Michalik:58936,
author = {Michalik, Marek and Hänsel, Michael and Quadakkers, Willem
J.},
title = {{E}ffect of water vapour on growth and adherence of chromia
scales on pure chromium},
volume = {67},
school = {RWTH Aachen},
type = {Dr. (Univ.)},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {PreJuSER-58936},
isbn = {978-3-89336-486-2},
series = {Schriften des Forschungszentrums Jülich. Reihe
Energietechnik / Energy Technology},
year = {2007},
note = {Record converted from VDB: 12.11.2012; RWTH Aachen, Diss.,
2007},
abstract = {The oxidation behaviour of chromium was studied in the
temperature range 950 to 1050$^{\circ}$C. A number of
atmospheres such as Ar-O$_{2}$, Ar-H$_{2}$-H$_{2}$O, and
more complex N$_{2}$-O$_{2}$-H$_{2}$O and
N$_{2}$-H$_{2}$-H$_{2}$O were used, to allow the effects of
oxygen and water vapour partial pressures to be determined.
It was shown that the oxide scale formed in Ar-O$_{2}$
environments was dependent on the oxygen partial pressure.
Decreasing the pO$_{2}$ in such gas mixtures lowered the
oxidation rate and improved scale adherence. Different
behaviour was found in Ar-H$_{2}$-H$_{2}$O. Scale adherence
remained good in all low pO$_{2}$ gases and decreasing the
pO$_{2}$ in the gas (this was done by using gases of higher
H$_{2}$/H$_{2}$O ratio) led to an increase in the oxidation
rate. The main finding of the work was that the oxide scale
formed on chromium in Ar-H$_{2}$O and Ar-H$_{2}$- H$_{2}$O
gases significantly differs from that formed in Ar-O$_{2}$.
It appeared that oxide grains were much smaller in low
pO$_{2}$ gases containing water vapour than in dry high
pO$_{2}$ gases. It is believed that this effect of water
vapour on the oxide morphology development is due to the
faster adsorption and dissociation of H$_{2}$O at the outer
surface compared with O$_{2}$, which enhance the inward
transport of oxygen ions to the metal/oxide interface. It is
proposed that increased oxygen grain boundary diffusion is
the dominant process but molecular transport of H$_{2}$ and
H$_{2}$O through the scale could also operate and contribute
to the inner scale growth. The tracer study combined with
SNMS techniques showed that in low pO$_{2}$ gases a
significant amount of the scale was formed at the
metal/oxide interface and this supports the observations
that smaller oxide grains promote inward oxygen transport.
It was also found that the extent of inward growth was
higher in Ar-H$_{2}$-H$_{2}$O than in Ar-H$_{2}$O gas. This
may indicate that the oxygen partial pressure of the gas or
the hydrogen partial pressure were also factors determining
the oxidation behaviour in low pO$_{2}$ gases. [...]},
cin = {IEF-2},
ddc = {620},
cid = {I:(DE-Juel1)VDB810},
pnm = {Rationelle Energieumwandlung},
pid = {G:(DE-Juel1)FUEK402},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://juser.fz-juelich.de/record/58936},
}