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   <subfield code="a">Influence of Hydrogen and Water Vapour on the Kinetics of Chromium Oxide Growth at High Temperature</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[S. Guillou, C. Cabet, C. Desgranges, L. Marchetti, Y. Wouters]</subfield>
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   <subfield code="a">In support of the selection of structural materials for heat exchangers in helium-cooled high temperature reactors, the oxidation behaviour of the Ni-base chromia-former alloy 230 was investigated at 850°C in diluted helium atmosphere with a low water vapour content. In such a media, the equivalent partial pressure of oxygen (imposed by the $$ P_{{{\text{H}}_{2} {\text{O}}}} $$/$$ P_{{{\text{H}}_{2}}} $$ ratio) is very low ($$ P_{{{\text{O}}_{ 2} }}^{\text{eq}} $$ around 10−16Pa). The equivalent partial pressure of oxygen has no straight influence on the parabolic rate constant (k p); on the other hand, $$ P_{{{\text{H}}_{2} }} $$ and $$ P_{{{\text{H}}_{2} {\text{O}}}} $$ demonstrate a complex influence on k p. Photoelectrochemistry analyses revealed that this oxide could simultaneously contain two types of cationic defects. Specific oxidation tests with D2O showed that the oxide scale also contains hydrogen. A mechanist model is proposed in order to describe the scale growth using both cationic defects. Those theoretical results show, at least qualitatively, how $$ P_{{{\text{H}}_{2} }} $$ and $$ P_{{{\text{H}}_{2} {\text{O}}}} $$ may concurrently influence the oxidation rate.</subfield>
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