mmme1029 Notes on the crystallisation of materials
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@ -771,3 +771,134 @@ of heat and electricity (they are insulators).
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Polymer foams are even better insulators because they have holes which lowers their density.
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</details>
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# Chemical Bonding of Materials
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Chemical bonds are what holds a material together in solid state.
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There are 5 main types of bonds:
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Type | Dissociation energy
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-------- | -------------------
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Ionic | 600 to 1500
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Covalent | 300 to 1200
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Metallic | 100 to 800
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Hydrogen | 4 to 23
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vdw | 0.4 to 4
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The dissociation energy is the energy required to break the bond, or the strength of the bond.
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## Materials and their Properties and Bonding
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### Ceramics and Glasses
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Ceramics and glasses are composed of mixed ionic and covalent bonding.
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Their strong and rigid bonds have no ability to slide past each other.
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This makes the materials brittle.
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### Metals
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Metals are based on metallic bonding (woah).
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This type of bonding *does* allow for ions to slide past each other, making metals ductile.
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### Polymers
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Polymer chains made of C-C covalent bonds are strong, like those found in ceramics.
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However, in thermoplastics polymers, the materials can yield by having the chains untangle and
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then align, as the chains slide past each other.
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This means that **stronger bonds between polymer chains means a higher yield stress in thermoplastic
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polymers**.
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# Crystallisation of Materials
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## Atomic Arrangement
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- No order
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- Short range order
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Silica glasses have short range order on the atomic scale.
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They are composed of regular SiO$_4$ units which all have the same bond length and bond angles.
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However, these units bond together irregularly, which results in different length chemical bonds
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and angles between the units, meaning they do not have any long range order.
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- Long range order
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## Cubic Unit Cells
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- Lattice Parameter --- One side of a unit cell
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The lattice parameter can be different for each side of a cell.
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- Simple cubic unit (SC):
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![](./images/vimscrot-2021-12-21T21:28:34,863875469+00:00.png)
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Lattice Parameter = 2r
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- Face centred cubic (FCC)
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![](./images/vimscrot-2021-12-21T21:44:21,618384089+00:00.png)
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- Body centred cubic (BCC)
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![](./images/vimscrot-2021-12-21T21:44:40,816535537+00:00.png)
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### Packing Factor
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$$\text{packing factor} = \frac{\text{ions per unit cell} \times V_{ion}}{V_{cell}}$$
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### Theoretical Density
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$$\text{theoretical density} = \frac{\text{ions per unit cell} \times m_{ion}}{V_{cell}}$$
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### Polymorphism
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Example of a polymorphic solid-state phase transfomration of iron at 1185 K and 1 atm:
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$$\text{Fe}_{\text{BCC}} \longleftrightarrow \text{Fe}_{\text{FCC}}$$
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Below 1185 K and at 1 atm, only BCC exists. Above 1185 K and at 1 atm, only FCC exists.
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### Points, Directions, Planes in a Cubic Unit Cell
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![](./images/vimscrot-2021-12-21T22:33:35,491930818+00:00.png)
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### Slip Systems in Metals
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Metal ions lying in close-packed planes and directions move more easily, increasing ductility.
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The combination of a close packed plane and direction is called a *slip system*.
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A close packed direction is where ions touch all the way along the direction.
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A close packed plane is where ions touch all the way on a plane.
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FCC metal ductility is mainly controlled by the *(111) slip plane*
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![](./images/vimscrot-2021-12-21T22:40:37,978916142+00:00.png)
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## X-Ray Diffraction (Bragg's Law)
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The wavelength of x-rays, $\lambda$, is roughly equal to the distance, $d$, between atom/ion layers.
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This allows x-rays to probe for $d$ via Bragg's Equation:
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![](./images/vimscrot-2021-12-21T22:44:15,147729727+00:00.png)
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Requirements for the x-rays:
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- Monochromatic
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- Coherent (phase difference of $2\pi n$ where n is any integer)
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- Parallel with each other
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The incoming x-rays 1 and 2 strike the rows of ions in the crystal and are diffracted, which can be
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considered reflection at the atomic level.
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The angle of incidence equals the angle of reflection.
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The outgoing x-rays 1 and 2 are coherent only if the extra path travelled by ray 2, $2d\sin\theta$
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is any multiple, $n$, of $\lambda$. Or:
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$$n\lambda = 2d\sin\theta$$
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This is Bragg's Law.
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