Long-term amorphisation of C+ and N2+ implanted layers on a uranium surface

被引:15
作者
Arkush, R
Mintz, MH
Kimmel, G
Shamir, N
机构
[1] Nucl Res Ctr Negev, IL-84190 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, IL-84105 Beer Sheva, Israel
关键词
actinide alloys; amorphization; X-ray diffraction;
D O I
10.1016/S0925-8388(02)00017-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ion implantation of C+ or N-2(+) on uranium surfaces produces crystalline compounds (uranium carbides or nitrides, respectively), which have been shown to provide excellent protection against ambient corrosion. Some long-term changes of these implanted layers were detected that even though not affecting the protection ability, still are of fundamental interest. The most prominent change is the amorphisation of the carbide or nitride layers, which takes place after a few years of air exposure. This amorphisation did not result from the oxidation of the layer (the formed oxides are much thinner than the thickness of the implanted layers), but is still assisted by air exposure (i.e., the amorphisation rates of samples kept under vacuum are much lower than those exposed to the ambient atmosphere). Some additional long-term changes in the layer compositions (transitions of UN2 to U2N3) and distributions (inward diffusion of the implanted ions) were also apparent. It is suggested that the presence of hydrogen in the implanted layer, originating from the dissociation of water molecules on the surface, may accelerate the amorphisation and the UN2 to U2N3 transition due to the possible increase in the diffusion constant. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:122 / 126
页数:5
相关论文
共 7 条
[1]   Passivation of uranium towards air corrosion by N2+ and C+ ion implantation [J].
Arkush, R ;
Mintz, MH ;
Shamir, N .
JOURNAL OF NUCLEAR MATERIALS, 2000, 281 (2-3) :182-190
[2]   URANIUM + WATER REACTION .2. EFFECT OF OXYGEN AND OTHER GASES [J].
BAKER, MM ;
LESS, LN ;
ORMAN, S .
TRANSACTIONS OF THE FARADAY SOCIETY, 1966, 62 (525P) :2525-&
[3]   HYDROGEN-INDUCED METAL ATOM REARRANGEMENTS IN PD3+XMN1-X ALLOYS WITH X-GREATER-THAN-OR-EQUAL-TO-0 USING TRANSMISSION ELECTRON-MICROSCOPY, ELECTRICAL RESISTIVITIES AND H-2 SOLUBILITIES [J].
FLANAGAN, TB ;
CRAFT, AP ;
NIKI, Y ;
BABA, K ;
SAKAMOTO, Y .
JOURNAL OF ALLOYS AND COMPOUNDS, 1992, 184 (01) :69-85
[4]   EVIDENCE OF COPIOUS VACANCY FORMATION IN NI AND PD UNDER A HIGH HYDROGEN PRESSURE [J].
FUKAI, Y ;
OKUMA, N .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 2-LETTERS & EXPRESS LETTERS, 1993, 32 (9A) :L1256-L1259
[5]   FORMATION OF SUPERABUNDANT VACANCIES IN PD HYDRIDE UNDER HIGH HYDROGEN PRESSURES [J].
FUKAI, Y ;
OKUMA, N .
PHYSICAL REVIEW LETTERS, 1994, 73 (12) :1640-1643
[6]   H-induced plastic deformation of Gd thin films studied by STM [J].
Pundt, A ;
Getzlaff, M ;
Bode, M ;
Kirchheim, R ;
Wiesendanger, R .
PHYSICAL REVIEW B, 2000, 61 (15) :9964-9967
[7]   The adsorption of H2O vs O-2 on beryllium [J].
Zalkind, S ;
Polak, M ;
Shamir, N .
SURFACE SCIENCE, 1997, 385 (2-3) :318-327