- Grain boundary
A grain boundary is the interface between two grains in a polycrystalline material. Grain boundaries disrupt the motion of dislocations through a material, so reducing crystallite size is a common way to improve strength, as described by the
Hall-Petchrelationship. Since grain boundaries are defects in the crystalstructure they tend to decrease the electrical and thermal conductivityof the material. The high interfacial energy and relatively weak bonding in most grain boundaries often makes them preferred sites for the onset of corrosion and for the precipitation of new phases from the solid. They are also important to many of the mechanisms of creep.
High and low angle boundaries
It is convenient to separate grain boundaries by the extent of the mis-orientation between the two grains. "Low angle grain boundaries" (LAGBs) are those with a misorientation less than about 11 degrees. Generally speaking they are composed of an array of
dislocations and their properties and structure are a function of the misorientation. In contrast the properties of "high angle grain boundaries" (HAGBs) whose misorientation is greater than about 11 degrees (the transition angle varies from 10-15 degrees depending on the material) are normally found to be independent of the misorientation. However there are 'special boundaries' at particular orientations whose interfacial energies are notably lower than those of general HAGBs.
The most simple boundary is that of a tilt boundary where the rotation axis is parallel to the boundary plane. This boundary can be conceived as forming from a single, contiguous
crystalliteor grain which is gradually bent by some external force. The energy associated with the elastic bending of the lattice can be reduced by inserting a dislocation, which is essentially a half-plane of atoms that act like a wedge, that creates a permanent misorientation between the two sides. As the grain is bent further, more and more dislocations must be introduced to accommodate the deformation resulting in a growing wall of dislocations - a low-angle boundary. The grain can now be considered to have split into two sub-grains of related crystallography but notably different orientations.
An alternative is a twist boundary where the misorientation occurs around an axis that is perpendicular to the boundary plane. This type of boundary incorporates two sets of screw dislocations. If the
Burgers vectors of the dislocations are orthogonal then the dislocations do not strongly interact and form a square network. In other cases the dislocations may interact to form a more complex hexagonal structure.
These concepts of tilt and twist boundaries represent somewhat idealised cases. The majority of boundaries are of a mixed-type, containing dislocations of different types and burgers vector, in order to create the best fit between the neighbouring grains.
While the dislocations in the boundary remain isolated and distinct the boundary can be considered to be low-angle. If deformation continues the density of dislocations will increase and so reduce the spacing between neighbouring dislocations. Eventually, the cores of the dislocations will begin to overlap and the ordered nature of the boundary will begin to break down. At this point the boundary can be considered to be high-angle and the original grain to have separated into two entirely separate grains.
In comparison to LAGBs, high-angle boundaries are considerably more disordered with large areas of poor fit and a comparatively open structure. Indeed, they were originally thought to be some form of amorphous or even liquid layer between the grain. However, this model could not explain the observed strength of grain boundaries and, after the invention of
electron microscopy, direct evidence of the grain structure meant the hypothesis had to be discarded. It is now accepted that a boundary consists of structural units which depend on both the misorientation of the two grains and the plane of the interface. The types of structural unit that exist can be related to the concept of the "coincidence site lattice" where regions of poor fit occur between points where the two lattices happen to fit together.
Enter the concept of coincident site lattice (CSL). The degree of fit (Σ) between the structures of the two grains is described by the
reciprocalof the ratio of coincidence sites to the total number of sites. Thus a boundary with high Σ might be expected to have a higher energy than one with low Σ. Low-angle boundaries, where the distortion is entirely accommodated by dislocations, are Σ1. Some other low Σ boundaries have special properties especially when the boundary plane is one that contains a high density of coincident sites.Examples include coherent twin boundaries (Σ3) and high-mobility boundaries in FCC materials (Σ7). Deviations from the ideal CSL orientation may be accommodated by local atomic relaxation or the inclusion of dislocations into the boundary.
Describing a boundary
A boundary can be described by the orientation of the boundary to the two grains and the 3-D rotation required to bring the grains into coincidence. Thus a boundary has 5 macroscopic
degrees of freedom. However, it is common to describe a boundary only as the orientation relationship of the neighbouring grains. Generally, the convenience of ignoring the boundary plane orientation, which is very difficult to determine, outweighs the reduced information.The relative orientation of the two grains is described using the rotation matrix:
Using this system the rotation angle θ is:
while the direction [uvw] of the rotation axis is:
The nature of the
crystallographyinvolved limits the misorientation of the boundary. A completely random polycrystal, with no texture, thus has a characteristic distribution of boundary misorientations (see figure). However, such cases are rare and most materials will deviate from this ideal to a greater or lesser degree.
The energy of a low-angle boundary is dependent on the degree of misorientation between the neighbouring grains up to the transition to high-angle status. In the case of simple "tilt boundaries" the energy of a boundary made up of dislocations with Burgers vector "b" and spacing "h" is predicted by the Read-Shockley equation:
where θ = b/h, γ0 = Gb/4 π(1-ν), A = 1 + ln(b/2 πr0), G is the
shear modulus, ν is poisson's ratio, and r0 is the radius of the dislocation core. It can be seen that as the energy of the boundary increases the energy per dislocation decreases. Thus there is a driving force to produce fewer, more misoriented boundaries (i.e grain growth).
The situation in high-angle boundaries is more complex. Although theory predicts that the energy will be a minimum for ideal CSL configurations, with deviations requiring dislocations and other energetic features, empirical measurements suggest the relationship is more complicated. Some predicted troughs in energy are found as expected while others missing or substantially reduced. Surveys of the available experimental data have indicated that simple relationships such as low Σ are misleading:
It is concluded that no general and useful criterion for low energy can be enshrined in a simple geometric framework. Any understanding of the variations of interfacial energy must take account of the atomic structure and the details of the bonding at the interface. [Stutton.]
The movement of grain boundaries (HAGB) has implications for
recrystallizationand grain growthwhile subgrain boundary (LAGB) movement strongly influences recoveryand the nucleation of recrystallization.
A boundary moves due to a pressure acting on it. It is generally assumed that the velocity is directly proportional to the pressure with the constant of proportionality being the mobility of the boundary. The mobility is strongly temperature dependent and often follows an Arrhenius type relationship:
The apparent activation energy (Q) may be related to the thermally activated atomistic processes that occur during boundary movement. However, there are several proposed mechanisms where the mobility will depend on the driving pressure and the assumed proportionality may break down.
It is generally accepted that the mobility of low-angle boundaries is much lower than that of high-angle boundaries. The following observations appear to hold true over a range of conditions:
* The mobility of low-angle boundaries is proportional to the pressure acting on it.
ratecontrolling process is that of bulk diffusion
* The boundary mobility increases with misorientation.
Since low-angle boundaries are composed of arrays of dislocations and their movement may be related to dislocation theory. The most likely mechanism, given the experimental data, is that of dislocation climb, rate limited by the diffusion of solute in the bulk. [Humphreys.]
The movement of high-angle boundaries occurs by the transfer of atoms between the neighbouring grains. The ease with which this can occur will depend on the structure of the boundary, itself dependent on the crystallography of the grains involved, impurity atoms and the temperature. It is possible that some form of diffusionless mechanism (akin to diffusionless phase transformations such as
martensite) may operate in certain conditions. Some defects in the boundary, such as steps and ledges, may also offer alternative mechanisms for atomic transfer.
Since a high-angle boundary is imperfectly packed compared to the normal lattice it has some amount of "free space" or "free volume" where solute atoms may possess a lower energy. As a result a boundary may be associated with a "solute atmosphere" that will retard its movement. Only at higher velocities will the boundary be able to break free of its atmosphere and resume normal motion.
Both low- and high-angle boundaries are retarded by the presence of particles via the so-called
zener pinningeffect. This effect is often exploited in commercial alloys to minimise or prevent recrystallizationor grain growthduring heat-treatment.
Segregation in materials
*cite journal | author=AP Sutton, RW Balluffi | title=Overview no. 61: On geometric criteria for low interfacial energy | journal=Acta Metallurgica | year=1987| volume=35 | issue=9 | pages= 2177–2201 | doi=10.1016/0001-6160(87)90067-8
*cite book | author=FJ Humphreys, M Hatherly | year=2004 | title=Recrystallisation and related anealing phenomena | publisher=Elsevier
*cite journal | author=RD Doherty; DA Hughes; FJ Humphreys; JJ Jonas; D Juul Jenson; ME Kassner; WE King; TR McNelley; HJ McQueen; AD Rollett | title=Current Issues In Recrystallisation: A Review | journal=Materials Science and Engineering | year=1997| volume=A238 | pages= 219–274
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