Difference between revisions of "Twinning"
From Online Dictionary of Crystallography
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<Font color="blue"> Macles </Font>(''Fr''). <Font color="black"> Geminati </Font>(''It'') | <Font color="blue"> Macles </Font>(''Fr''). <Font color="black"> Geminati </Font>(''It'') | ||
− | = Oriented association = | + | = Oriented association and twinning = |
− | Crystals (also called individuals) belonging to the same phase form an oriented association if they can be brought to the same crystallographic orientation by translation, rotation or reflection. Individuals related by a translation form a parallel association. Individuals related either by a | + | Crystals (also called individuals) belonging to the same phase form an oriented association if they can be brought to the same crystallographic orientation by translation, rotation or reflection. Individuals related by a translation form a ''parallel association''; strictly speaking these individuals have the same orientation even without applying a translation. Individuals related either by a reflection (mirror plane or centre of symmetry) or a rotation form a ''twin''. |
+ | |||
+ | An element of symmetry crystallographically relating differently oriented crystals cannot belong to the individual. The element of symmetry that relates the indivduals of a twin is called ''twinning element of symmetry'' and the connected operation is a ''twinning operation of symmetry''. | ||
* '''isotropic media''' | * '''isotropic media''' |
Revision as of 12:44, 18 April 2006
Contents
Twins
Other languages
Macles (Fr). Geminati (It)
Oriented association and twinning
Crystals (also called individuals) belonging to the same phase form an oriented association if they can be brought to the same crystallographic orientation by translation, rotation or reflection. Individuals related by a translation form a parallel association; strictly speaking these individuals have the same orientation even without applying a translation. Individuals related either by a reflection (mirror plane or centre of symmetry) or a rotation form a twin.
An element of symmetry crystallographically relating differently oriented crystals cannot belong to the individual. The element of symmetry that relates the indivduals of a twin is called twinning element of symmetry and the connected operation is a twinning operation of symmetry.
- isotropic media
the linear coefficient of thermal expansion, α, relates the relative variation (Δℓ/ℓ) of the length ℓ of a bar to the temperature variation ΔT. In the first order approximation it is given by:
α = (Δ ℓ/ℓ) /Δ T
- anisotropic media
the deformation is described by the strain tensor uij and the coefficient of thermal expansion is represented by a rank 2 tensor, αij, given by:
αij = uij / Δ T.
Volume thermal expansion
The volume thermal expansion, β, relates the relative variation of volume Δ V/V to Δ T:
- isotropic media
β = Δ V/V Δ T = 3 α,
- anisotropic media
it is given by the trace of α ij:
β = Δ V/V Δ T = α 11 + α 22 + α 33.
Grüneisen relation
The thermal expansion of a solid is a consequence of the anharmonicity of interatomic forces. The anharmonicity is most conveniently accounted for by means of the so-called `quasiharmonic approximation', assuming the lattice vibration frequencies to be independent of temperature but dependent on volume. This approach leads to the Grüneisen relation that relates the thermal expansion coefficients and the elastic constants:
- isotropic media
β = γ κ cV/V
where γ is the average Grüneisen parameter, κ the isothermal compressibility, cV the specific heat at constant volume.
- anisotropic media
γij = cijklT αkl V/cV
where the Grüneisen parameter is now represented by a second rank tensor, κij, and cijklT is the elastic stiffness tensor at constant temperature.
For details see Sections 1.4.2 and 2.1.2.8 of International Tables Volume D.
Measurement
The coefficient of thermal expansion can be measured using diffraction methods (for powder diffraction methods, see Section 2.3 of International Tables Volume C, for single crystal methods, see Section 5.3 of International Tables Volume C), optical methods (interferometry) or electrical methods (pushrod dilatometry methods or capacitance methods). For details see Section 1.4.3 of International Tables Volume D.
See also
Chapters 2.3 and 5.3, International Tables Volume C
Chapters 1.4 and 2.1, International Tables of Crystallography, Volume D