TY - JOUR
T1 - Heat treatment effects on the surface chemisorption behavior of strained uranium
T2 - The H2O/U reaction
AU - Tiferet, E.
AU - Mintz, M. H.
AU - Zalkind, S.
AU - Jacob, I.
AU - Shamir, N.
N1 - Funding Information:
This work was partially supported by grants from the Israel Council for Higher Education and the Israel Atomic Energy Commission and the Ministry of National Infrastructure, Division of R&D. The authors wish to thank G. Kimmel for a fruitful discussion.
PY - 2007/11/1
Y1 - 2007/11/1
N2 - The initial interaction of H2O vapor with polycrystalline uranium surfaces was studied with samples initially strained, then strain relieved by heat treatments, performed in the temperature range up to ∼650 K. The chemisorption characteristics of these surfaces were studied by a combination of direct recoils spectrometry and X-ray photoelectron spectroscopy. X-ray diffraction measurements were used to determine the level of strain relief induced by each of the heat treatments. For all the samples, full water dissociation on the metal surface is observed. The reactivity of the samples towards water is clearly strain dependent, with the sticking coefficient decreasing as strain is relieved. It also seems that for strained samples the initial growth of the oxide is mostly inwards, while for the more relaxed samples lateral growth is dominant. Two interesting phenomena were observed for specific samples. For the 420 K relieved sample, partial dissociation process is observed on top of the forming oxide, in contrast to the full dissociation observed for the other samples. For the ∼650 K relieved sample, clustering of the adsorbed hydrogen atoms (resulted by water dissociation) on the metal surface is observed, in contrast to the homogeneous dispersion of H, occurring on the surface of all other samples. These two phenomena will further be studied in conjunction with microscopic metallurgical observations.
AB - The initial interaction of H2O vapor with polycrystalline uranium surfaces was studied with samples initially strained, then strain relieved by heat treatments, performed in the temperature range up to ∼650 K. The chemisorption characteristics of these surfaces were studied by a combination of direct recoils spectrometry and X-ray photoelectron spectroscopy. X-ray diffraction measurements were used to determine the level of strain relief induced by each of the heat treatments. For all the samples, full water dissociation on the metal surface is observed. The reactivity of the samples towards water is clearly strain dependent, with the sticking coefficient decreasing as strain is relieved. It also seems that for strained samples the initial growth of the oxide is mostly inwards, while for the more relaxed samples lateral growth is dominant. Two interesting phenomena were observed for specific samples. For the 420 K relieved sample, partial dissociation process is observed on top of the forming oxide, in contrast to the full dissociation observed for the other samples. For the ∼650 K relieved sample, clustering of the adsorbed hydrogen atoms (resulted by water dissociation) on the metal surface is observed, in contrast to the homogeneous dispersion of H, occurring on the surface of all other samples. These two phenomena will further be studied in conjunction with microscopic metallurgical observations.
KW - Actinide alloys and compounds
KW - Gas-solid reactions
KW - Ion impact
KW - Oxidation
KW - Photoelectron spectroscopies
UR - http://www.scopus.com/inward/record.url?scp=34548137408&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2006.10.103
DO - 10.1016/j.jallcom.2006.10.103
M3 - Article
AN - SCOPUS:34548137408
SN - 0925-8388
VL - 444-445
SP - 177
EP - 183
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
IS - SPEC. ISS.
ER -