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21-Mat-A5 Phase Transformations and Thermal Treatment · May 2018

Question 1 of 8: Slip Systems, Stereographic Texture Representation and Twinning

Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)

Notes on this paper

Paper format. National Exams, May 2018 — 10-Met-A5, Mechanical Behaviour and Fracture of Materials. Three hours, closed book, any non-communicating calculator permitted. Eight questions of 20 marks each; the rubric states that five questions constitute a complete paper and that only the first five appearing in the answer book are marked. All eight are answered here, because this set is a study resource rather than an exam script. Several sub-parts explicitly call for an essay-format answer, and the rubric rewards clarity and organisation, so those answers are written as structured prose rather than as note form.

Note on the exam title

Nothing on the paper is a phase-transformation or heat-treatment question in the TTT/CCT, hardenability or tempering sense; the syllabus actually examined is crystallography of slip and twinning, dislocation theory, creep, fatigue, toughness and fracture mechanics, and safe-life fatigue design.

Reference texts. The answers below are keyed to the works normally recommended for this syllabus code:


Question 1: Slip Systems, Stereographic Texture Representation and Twinning (20 marks)

Question text not reproduced: the examination questions are © Engineers and Geoscientists BC. Open the official past paper (linked at the top of this page) to read the question, then follow the worked solution below.

1.1 — (a) Slip systems, and how many are independent in FCC

A slip system is the combination of a specific crystallographic plane (the slip plane, the plane of highest atomic density) and a specific crystallographic direction lying in that plane (the slip direction, the direction of shortest atomic repeat distance) on which dislocation glide occurs. Both are set by the crystal structure: close-packed planes and close-packed directions minimise the Burgers vector and hence the energy of the glide dislocation.

In FCC the slip plane family is $\{111\}$ (four distinct planes) and the slip direction family is $\langle110\rangle$ (three independent directions lying in each plane), giving $4\times3=\mathbf{12}$ slip systems in total. Not all twelve are crystallographically independent, however: von Mises showed that an arbitrary shape change of a polycrystalline grain requires five independent slip systems, and of the twelve FCC systems only five are linearly independent (the other seven are expressible as combinations of those five, because the twelve systems are not all geometrically distinct strain contributors). FCC readily supplies the required five, which is the crystallographic reason FCC metals (Cu, Al, Ni, austenitic steel) are reliably ductile in polycrystalline form, in contrast to HCP metals (Question 4c).

1.2 — (b) Standard $(100)$ stereographic projection and texture

A stereographic projection maps the orientation of every plane in a crystal onto a single flat diagram by projecting the plane's pole (its unit normal) from the far pole of a reference sphere onto the equatorial plane. For a cubic crystal, the standard $(100)$ projection is centred on the $[100]$ pole, with the primitive great-circle net (a Wulff net) providing angular coordinates, and the low-index poles $\{100\}$, $\{110\}$ and $\{111\}$ plotted at their known angular separations.

[100] [010] [0-10] [001] [00-1] {111} {110} Rolling texture, e.g. {110}<112> clustered poles = preferred orientation; a random polycrystal gives a uniform scatter
Left: the standard $(100)$ stereographic projection of a cubic crystal, with the $\{100\}$, $\{110\}$ and $\{111\}$ pole positions plotted at their known angular separations from $[100]$. Right: crystallographic texture is represented on the same kind of net (a pole figure) by plotting the same pole, e.g. $\{110\}$, for every grain in a real polycrystal; a random polycrystal scatters uniformly (grey dots), while a textured one — here a rolling texture with $\{110\}\langle112\rangle$ character — clusters into a small number of intensity maxima (red).

The key distinction the sketch must communicate is between the single-crystal projection on the left, which plots every symmetry-equivalent pole of one crystal at its exact geometric position, and a pole figure on the right, which plots one specific pole (say $\{110\}$) repeatedly, once per grain, for a whole polycrystalline sample. A random polycrystal produces a uniform density of points over the net; a textured polycrystal — produced by rolling, drawing or recrystallisation — produces intensity maxima at the orientations preferentially selected by the deformation or annealing history, exactly as sketched for the $\{110\}\langle112\rangle$ rolling texture common in BCC sheet steel.

1.3 — (c) Twinning systems in FCC

A twinning system is, analogously to a slip system, a specific crystallographic plane (the twin/composition plane, across which the lattice is mirrored) together with a specific shear direction in that plane (the twinning shear direction) that together produce a homogeneous simple shear reorienting a thin lamella of the crystal into its mirror-twin orientation. Unlike slip, twinning shear is directional: shearing the correct sense produces the twin (a low-energy, mechanically favourable reorientation), while shearing the opposite sense along the same plane and direction does not reproduce a twin at all, so twin systems are not related by a simple $\pm$ sign the way slip systems are.

FCC twins on $\{111\}$ planes in the $\langle112\rangle$ shear direction. There are four distinct $\{111\}$ planes, and each contains three $\langle112\rangle$-type directions that lie in it, giving $4\times3=\mathbf{12}$ possible twinning systems — numerically the same count as the FCC slip systems, because the same $\{111\}\langle$in-plane$\rangle$ geometry underlies both, but twinning uses the $\langle112\rangle$ partial-dislocation shear direction rather than the $\langle110\rangle$ full-dislocation slip direction.

1.4 — (d) Maximum number of distinct twin traces, BCC vs. FCC

A twin trace is the line where a twin plane intersects a polished and etched surface; its orientation on the section depends only on the twin plane's orientation in space, not on the shear direction within it. The number of distinguishable trace orientations that can appear is therefore the number of crystallographically distinct planes in the twinning-plane family, counting a plane and its geometric opposite ($hkl$ and $\overline{hkl}$, which define the same infinite plane) only once.

  1. FCC: count the distinct $\{111\}$ planes. Indices $(1,1,1)$ with all sign combinations give $2^3=8$ directed normals; dividing by 2 for the $\pm$ plane equivalence gives $$8/2=\boxed{4\text{ distinct }\{111\}\text{ planes}}$$
  2. BCC: count the distinct $\{112\}$ planes. Indices $(1,1,2)$ in any of the 3 positional orderings, each with $2^3=8$ sign combinations, gives $3\times8=24$ directed normals; dividing by 2 gives $$24/2=\boxed{12\text{ distinct }\{112\}\text{ planes}}$$

So a heavily deformed FCC crystal can show at most 4 differently oriented twin traces on a given section, while a heavily deformed BCC crystal (which twins on $\{112\}\langle111\rangle$) can show at most 12. This higher multiplicity is consistent with BCC's greater propensity to twin under shock or low-temperature/high-rate loading, where more twin-plane variants compete to accommodate the imposed strain.

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