Point Defect Absorption and Dislocation Loop Formation at Grain Boundaries in Hvem-Irradiated Zr and Its Alloys:1. Influence of Solute Addition

Author(s):  
R.A. Herring ◽  
M. Griffiths ◽  
M.H Loretto ◽  
R.E. Smallman

Because Zr is used in the nuclear industry to sheath fuel and as structural component material within the reactor core, it is important to understand Zr's point defect properties. In the present work point defect-impurity interaction has been assessed by measuring the influence of grain boundaries on the width of the zone denuded of dislocation loops in a series of irradiated Zr alloys. Electropolished Zr and its alloys have been irradiated using an AEI EM7 HVEM at 1 MeV, ∼675 K and ∼10-6 torr vacuum pressure. During some HVEM irradiations it has been seen that there is a difference in the loop nucleation and growth behaviour adjacent to the grain boundary as compared with the mid-grain region. The width of the region influenced by the presence of the grain boundary should be a function of the irradiation temperature, dose rate, solute concentration and crystallographic orientation.

2014 ◽  
Vol 70 (a1) ◽  
pp. C32-C32
Author(s):  
Peter Rudolph

The quality of single crystals, epitaxial layers and devices made there from are very sensitively influenced by structural and atomistic deficiencies generated during the crystal growth. Crystalline imperfections comprise point defects, dislocations, grain boundaries, second-phase particles. Over more than a half-century of the development of crystal growth, most of the important defect-forming mechanisms have become well understood [1-2]. As a result, the present state of technology makes it possible to produce crystals of remarkably high quality. However, that is not to say that all problems are already solved. For instance, in comparison with silicon the point defect dynamics in semiconductor and oxide compounds is not nearly as well understood. The density of equivalent defect types and antisites in each sub-lattice is determined by deviation from stoichiometry. Their charge state depends on the Fermi level position leading via interaction with dopants to certain compensation level and complex formation. One measure proves to be the in situ control of stoichiometry. Due to high-temperature dislocation dynamics heterogeneous dislocation substructures are formed. Both, acting thermo-mechanical stress and given point defect situation force the dislocation to glide and climb. In the course of enthalpy minimization the long-range character of dislocation interaction produces agglomerates and patterns with polygonized cell walls, i.e. small angle grain boundaries [3]. Thanks to the rules of correspondence of Taylor and Kuhlmann-Wilsdorf one is able to estimate the interaction between shear stress, dislocation density and cell diameter (Fig.). In epitaxy the Nye tensor, describing dislocation distribution inhomogeneity, affects the layer stress considerably. The growth under minimum stress, solution hardening and in situ stoichiometry control are effective counteracting methods. One of the most serious consequences during cooling down of as-grown crystals is the point defect condensation in precipitates and micro-voids decorating dislocation patterns or inducing high mechanical misfit stress that generates dislocation loops. It proves to be favourable to anneal the crystal a few degrees below the melting point in order to dissolve the particles and re-diffuse their into the crystal matrix.


Author(s):  
J. Briceno-Valero ◽  
R. Gronsky

Studies of grain boundary segregation in metallurgical systems are traditionally based upon the premise that grain boundaries are more likely sites for solute atoms than their surrounding grains. This idea is manifested in experimnental studies which distinguish the solute concentration at boundaries from that of grain interiors using various spectroscopic techniques, including more recently, energy dispersive X-ray analysis in TEM/STEM instruments. A typical study therefore usually consists of spot or line scans across a grain boundary plane in order to detect concentration gradients at the boundary region. It has also been pointed out that there are rather severe problems in quantitatively determining the absolute solute concentration within the grain boundary, and data correction schemes for this situation have been proposed.


Author(s):  
E. L. Hall

The resistance of stainless steel to sensitization can be increased by reducing the carbon content, since sensitization is caused by the formation of chromium-rich carbides at grain boundaries which depletes the boundary region of chromium. The reduction in carbon content also lowers the strength of the steel, but this can be counteracted by adding nitrogen, leading to a series of low-carbon high-nitrogen alloys which are promising candidates for applications in the nuclear industry. However, the effect of nitrogen on the phase relationships in stainless steel are complex, and the purpose of this study is to examine these effects.Samples of 316 stainless steel with 16 w/o Cr, 9.8 w/o Ni, 2.5 w/o Mo, 0.03 w/o C, and 0.06-0.16 w/o N which had been solutionized and then aged at 600-700°C for 3-300 hours were used. Grain boundary phases were identified using electron diffraction, and grain boundary chemistry was measured using X-ray spectroscopy with a 10nm probe, either positioned directly on the boundary or stepped across the boundary with a spatial resolution of 50nm. The Cliff-Lorimer method was used to quantify the x-ray results.


1991 ◽  
Vol 229 ◽  
Author(s):  
A. H. King

AbstractWe present a review of systematic studies of diffusion induced grain boundary migration (DIGM). The results are compared with structural models for the grain boundaries in order to assess the effects of structure upon DIGM. The nucleation of DIGM is also assessed in the light of grain boundary structure and it is demonstrated that changes of grain boundary solute concentration can induce large enough energy changes to drive novel grain boundary dissociation reactions.


Nanoscale ◽  
2017 ◽  
Vol 9 (44) ◽  
pp. 17293-17302 ◽  
Author(s):  
William J. Bowman ◽  
Madeleine N. Kelly ◽  
Gregory S. Rohrer ◽  
Cruz A. Hernandez ◽  
Peter A. Crozier

The enhancement of grain boundary oxygen ionic conductivity by four orders of magnitude in an electroceramic is explicitly shown to result from modulation of local grain boundary composition at the atomic level.


1991 ◽  
Vol 240 ◽  
Author(s):  
H. G. Robinson ◽  
M. D. Deal ◽  
D. A. Stevenson ◽  
K. S. Jones

ABSTRACTRecent experimental results indicate that diffusion of implanted p-type dopants in GaAs is time dependent under certain conditions. For Mg implanted at a dose of 1 × 1014 cm−2, the diffusion is constant for approximately an hour, then decreases by an order of magnitude or more. Be implanted at 1 × 1013 and 1 ×1014 cm−2 exhibits similar behavior, but with a shorter time before the diffusivity decreases. The diffusivity in 1 × 1013 Mg cm−2 implants, in contrast, remains constant for up to 16 hours. TEM micrographs of Be and Mg implants reveal dislocation loops in the higher dose samples, but not in the lower dose ones. During annealing, the loops grow and decrease in density, eventually disappearing completely from the crystal. This annealing of the loops appears to correlate to the time dependence of the diffusion. This behavior can be explained in terms of the substitutional-interstitial diffusion (SID) mechanism and point defect equilibria.


2004 ◽  
Vol 467-470 ◽  
pp. 1045-1050 ◽  
Author(s):  
Koenraad G.F. Janssens ◽  
Elizabeth A. Holm ◽  
Stephen M. Foiles

In this paper we discuss the principles of a combined approach to solve the problem of solute drag as it occurs in microstructure evolution processes such as grain growth, recrystallization and phase transformation. A recently developed irregular grid cellular automaton is used to simulate normal grain growth, in which the energy of the grain boundaries is the driving force. A new, discrete diffusion model is used to simulate solute segregation to the grain boundaries. The local concentration of the solute is then taken into account in the calculation of the local grain boundary mobility and/or grain boundary energy, thereby constituting a drag force. The relation between solute concentration and grain boundary mobility/energy is derived from molecular dynamics simulations.


Author(s):  
J. W. Matthews ◽  
W. M. Stobbs

Many high-angle grain boundaries in cubic crystals are thought to be either coincidence boundaries (1) or coincidence boundaries to which grain boundary dislocations have been added (1,2). Calculations of the arrangement of atoms inside coincidence boundaries suggest that the coincidence lattice will usually not be continuous across a coincidence boundary (3). There will usually be a rigid displacement of the lattice on one side of the boundary relative to that on the other. This displacement gives rise to a stacking fault in the coincidence lattice.Recently, Pond (4) and Smith (5) have measured the lattice displacement at coincidence boundaries in aluminum. We have developed (6) an alternative to the measuring technique used by them, and have used it to find two of the three components of the displacement at {112} lateral twin boundaries in gold. This paper describes our method and presents a brief account of the results we have obtained.


Author(s):  
C. W. Price

Little evidence exists on the interaction of individual dislocations with recrystallized grain boundaries, primarily because of the severely overlapping contrast of the high dislocation density usually present during recrystallization. Interesting evidence of such interaction, Fig. 1, was discovered during examination of some old work on the hot deformation of Al-4.64 Cu. The specimen was deformed in a programmable thermomechanical instrument at 527 C and a strain rate of 25 cm/cm/s to a strain of 0.7. Static recrystallization occurred during a post anneal of 23 s also at 527 C. The figure shows evidence of dissociation of a subboundary at an intersection with a recrystallized high-angle grain boundary. At least one set of dislocations appears to be out of contrast in Fig. 1, and a grainboundary precipitate also is visible. Unfortunately, only subgrain sizes were of interest at the time the micrograph was recorded, and no attempt was made to analyze the dislocation structure.


Author(s):  
D. B. Williams ◽  
A. D. Romig

The segregation of solute or imparity elements to grain boundaries can occur by three well-defined processes. The first is Gibbsian segregation in which an element of minimal matrix solubility confines itself to a monolayer at the grain boundary. Classical examples include Bi in Cu and S or P in Fe. The second process involves the depletion of excess matrix solute by volume diffusion to the boundary. In the boundary, the solute atoms diffuse rapidly to precipitates, causing them to grow by the ‘collector-plate mechanism.’ Such grain boundary diffusion is thought to initiate “Diffusion-Induced Grain Boundary Migration,” (DIGM). This process has been proposed as the origin of eutectoid transformations or discontinuous grain boundary reactions. The third segregation process is non-equilibrium segregation which result in a solute build-up around the boundary because of solute-vacancy interactions.All of these segregation phenomena usually occur on a sub-micron scale and are often affected by the nature of the grain boundary (misorientation, defect structure, boundary plane).


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