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@@ -500,7 +500,7 @@ E &= \frac \sigma \epsilon = 2513836.686 = 2.5\times10^6 \text{ Pa}
## Poisson's Ratio
For most materiajs, their cross sectionts change when they are stretched or compressed.
For most materials, their cross sectionts change when they are stretched or compressed.
This is to keep their volume constant.
$$ \epsilon_x = \frac {\Delta L}{L_0} $$

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@@ -631,3 +631,274 @@ bonds between the surface of the fibre and matrix.
Kevlar/Epoxy | 1200 | 20
(All units in MPa)
# Thermal Properties of Materials
## Specific Heat Capacity
How much heat energy is required to raise the temperature of a body by one unit:
$$ C_p = \frac{\Delta E}{m\Delta T} $$
where $c$ is specific heat capacity.
It is measured at a constant pressure, usually $1.013\times 10^5$ Pa.
## Molar Heat Capacity
$$C_pm = \frac{\Delta E}{n\Delta T}$$
<details>
<summary>
#### What is a mole?
</summary>
> The mole (symbol: mol) is the base unit of amount of substance in the International System of
> Units (SI).
> It is defined as exactly $6.02214076\times 10^{23}$ elementary entities ("particles")
~ [Wikipedia: Mole (unit)](https://en.wikipedia.org/wiki/Mole_(unit))
<details>
<details>
<summary>
#### How Much Does a mol of Something weigh?
</summary>
A mol of an element weighs its relative atomic mass ($A_r$) but in grams.
For example, Carbon-12 has an $A_r$ of 12 (as it's made of 6 neutrons, 6 protons, and 6 electrons
which have negligible mass) so a mol of Carbon-12 has a mass of 12 g.
</details>
## Thermal Expansion
<details>
<summary>
### Origin of Thermal Expansion
</summary>
All atomic bonds vibrate, on the magnitude of gigahertz.
The bonds vibrate about a mean positoin and the vibration is a simple harmonic motion.
From the graph below you can see that as energy (in the form of heat) is supplied to the bonds,
the amplitude of the vibrations get larger and larger.
You can also see the mean position of the bond gets further and further away, meaning the volume
of the material also is increasing.
The mean position of the bond is what dictates the volume, as this means the inter-atomic
separation increases.
![Morse Potential Graph](./images/vimscrot-2021-12-21T19:51:58,667328620+00:00.png)
Morse potential is the energy well between 2 bonded atoms.
The graph is asymmetric due to the repulsion experienced by atoms as they apporach.
</details>
### Linear Coefficient of Thermal Expansion
$$\alpha_L = \frac{\Delta L}{L_0 \Delta T}$$
where $L$ is the sample length.
<details>
<summary>
#### Example 1
A 1 m long bar of aluminium metal cools in the solid state from 660 \textdegree{}C to
25 \textdegree{}C.
Calculate the length of the bar after it cools down, given $\alpha_L = 25\times10^{-6}$ K$^{-1}$.
</summary>
\begin{align*}
l_0 &= 1 \\
\Delta T &= T_f - T_0 = 25 - 660 = -635 \\
\\
\alpha_L &= \frac{l_f - l_0}{l_0 \Delta T} \\
\alpha_L l_0 \Delta T &= l_f - l_0 \\
l_f &= \alpha_L l_0 \Delta T + l_0 = 0.984
\end{align*}
</details>
### Linear Thermal Expansion and Isotropism
Since isotropic solids have the same properties in all directions, you can say that for an
isotropic solid:
$$\alpha_V = 3\alpha_L = \frac{\Delta V}{V_0 \Delta T}$$
### Reasons to Care About Thermal Expansion
- A coating on a material may fail if the thermal expansion coefficients do not match
- A brittle material may thermally shock and fracture due to thermal expansion mismatch between
the ouside and inside, especially if the material is not very thermally conductive
## Thermal Conductivity
Thermal conductivity is the rate at which heat power is transferred through a material.
$$\frac{Q}{A} = k \frac{\Delta T}{\Delta x}$$
where $Q$ is heat power, $A$ is area of the surface, $\frac{\Delta T}{\Delta x}$ is the
temperature gradient, and $k$ is the thermal conductivity constant.
<details>
<summary>
### Origin of Thermal Conductivity
</summary>
Heat is transferred through materials by electrons (and partially by atomic vibrations)
Metals have high thermal conductivity as their delocalised 'sea' electrons are about to move about
easily.
This makes them excellent conductors of heat and electricity.
Ceramics, glasses, and polymers do not have delocalised electrons and are therefore poor conductors
of heat and electricity (they are insulators).
Polymer foams are even better insulators because they have holes which lowers their density.
</details>
# Chemical Bonding of Materials
Chemical bonds are what holds a material together in solid state.
There are 5 main types of bonds:
Type | Dissociation energy
-------- | -------------------
Ionic | 600 to 1500
Covalent | 300 to 1200
Metallic | 100 to 800
Hydrogen | 4 to 23
vdw | 0.4 to 4
The dissociation energy is the energy required to break the bond, or the strength of the bond.
## Materials and their Properties and Bonding
### Ceramics and Glasses
Ceramics and glasses are composed of mixed ionic and covalent bonding.
Their strong and rigid bonds have no ability to slide past each other.
This makes the materials brittle.
### Metals
Metals are based on metallic bonding (woah).
This type of bonding *does* allow for ions to slide past each other, making metals ductile.
### Polymers
Polymer chains made of C-C covalent bonds are strong, like those found in ceramics.
However, in thermoplastics polymers, the materials can yield by having the chains untangle and
then align, as the chains slide past each other.
This means that **stronger bonds between polymer chains means a higher yield stress in thermoplastic
polymers**.
# Crystallisation of Materials
## Atomic Arrangement
- No order
- Short range order
Silica glasses have short range order on the atomic scale.
They are composed of regular SiO$_4$ units which all have the same bond length and bond angles.
However, these units bond together irregularly, which results in different length chemical bonds
and angles between the units, meaning they do not have any long range order.
- Long range order
## Cubic Unit Cells
- Lattice Parameter --- One side of a unit cell
The lattice parameter can be different for each side of a cell.
- Simple cubic unit (SC):
![](./images/vimscrot-2021-12-21T21:28:34,863875469+00:00.png)
Lattice Parameter = 2r
- Face centred cubic (FCC)
![](./images/vimscrot-2021-12-21T21:44:21,618384089+00:00.png)
- Body centred cubic (BCC)
![](./images/vimscrot-2021-12-21T21:44:40,816535537+00:00.png)
### Packing Factor
$$\text{packing factor} = \frac{\text{ions per unit cell} \times V_{ion}}{V_{cell}}$$
### Theoretical Density
$$\text{theoretical density} = \frac{\text{ions per unit cell} \times m_{ion}}{V_{cell}}$$
### Polymorphism
Example of a polymorphic solid-state phase transfomration of iron at 1185 K and 1 atm:
$$\text{Fe}_{\text{BCC}} \longleftrightarrow \text{Fe}_{\text{FCC}}$$
Below 1185 K and at 1 atm, only BCC exists. Above 1185 K and at 1 atm, only FCC exists.
### Points, Directions, Planes in a Cubic Unit Cell
![](./images/vimscrot-2021-12-21T22:33:35,491930818+00:00.png)
### Slip Systems in Metals
Metal ions lying in close-packed planes and directions move more easily, increasing ductility.
The combination of a close packed plane and direction is called a *slip system*.
A close packed direction is where ions touch all the way along the direction.
A close packed plane is where ions touch all the way on a plane.
FCC metal ductility is mainly controlled by the *(111) slip plane*
![](./images/vimscrot-2021-12-21T22:40:37,978916142+00:00.png)
## X-Ray Diffraction (Bragg's Law)
The wavelength of x-rays, $\lambda$, is roughly equal to the distance, $d$, between atom/ion layers.
This allows x-rays to probe for $d$ via Bragg's Equation:
![](./images/vimscrot-2021-12-21T22:44:15,147729727+00:00.png)
Requirements for the x-rays:
- Monochromatic
- Coherent (phase difference of $2\pi n$ where n is any integer)
- Parallel with each other
The incoming x-rays 1 and 2 strike the rows of ions in the crystal and are diffracted, which can be
considered reflection at the atomic level.
The angle of incidence equals the angle of reflection.
The outgoing x-rays 1 and 2 are coherent only if the extra path travelled by ray 2, $2d\sin\theta$
is any multiple, $n$, of $\lambda$. Or:
$$n\lambda = 2d\sin\theta$$
This is Bragg's Law.

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@@ -466,3 +466,41 @@ M_{OO} &= F_py_p = \int_{area}\! \rho gh^2 \,\mathrm{d}A \\
\\
y_p = \frac{M_{OO}}{F_p}
\end{align*}
## Buoyancy
### Archimedes Principle
> The resultant upwards force (buoyancy force) on a body wholly or partially immersed in a fluid is
> equal to the weight of the displaced fluid.
When an object is in equilibrium the forces acting on it balance.
For a floating object, the upwards force equals the weight:
$$mg = \rho Vg$$
Where $\rho$ is the density of the fluid, and $V$ is the volume of displaced fluid.
### Immersed Bodies
As pressure increases with depth, the fluid exerts a resultant upward force on a body.
There is no horizontal component of the buoyancy force because the vertiscal projection of the body
is the same in both directions.
### Rise, Sink, or Float?
- $F_B = W$ \rightarrow equilirbrium (floating)
- $F_B > W$ \rightarrow body rises
- $F_B < W$ \rightarrow body sinks
### Centre of Buoyancy
Buoyancy force acts through the centre of gravity of the volume of fluid displaced.
This is known as the centre of buoyancy.
The centre of buoyancy does not in general correspond to the centre of gravity of the body.
If the fluid density is constant the centre of gravity of the displaced fluid is at the centroid of
the immersed volume.
![](./images/vimscrot-2021-12-21T15:08:22,285753421+00:00.png)