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@@ -500,7 +500,7 @@ E &= \frac \sigma \epsilon = 2513836.686 = 2.5\times10^6 \text{ Pa}
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## Poisson's Ratio
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For most materiajs, their cross sectionts change when they are stretched or compressed.
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For most materials, their cross sectionts change when they are stretched or compressed.
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This is to keep their volume constant.
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$$ \epsilon_x = \frac {\Delta L}{L_0} $$
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@@ -631,3 +631,274 @@ bonds between the surface of the fibre and matrix.
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Kevlar/Epoxy | 1200 | 20
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(All units in MPa)
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# Thermal Properties of Materials
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## Specific Heat Capacity
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How much heat energy is required to raise the temperature of a body by one unit:
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$$ C_p = \frac{\Delta E}{m\Delta T} $$
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where $c$ is specific heat capacity.
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It is measured at a constant pressure, usually $1.013\times 10^5$ Pa.
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## Molar Heat Capacity
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$$C_pm = \frac{\Delta E}{n\Delta T}$$
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<details>
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<summary>
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#### What is a mole?
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</summary>
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> The mole (symbol: mol) is the base unit of amount of substance in the International System of
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> Units (SI).
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> It is defined as exactly $6.02214076\times 10^{23}$ elementary entities ("particles")
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~ [Wikipedia: Mole (unit)](https://en.wikipedia.org/wiki/Mole_(unit))
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<details>
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<details>
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<summary>
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#### How Much Does a mol of Something weigh?
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</summary>
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A mol of an element weighs its relative atomic mass ($A_r$) but in grams.
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For example, Carbon-12 has an $A_r$ of 12 (as it's made of 6 neutrons, 6 protons, and 6 electrons
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which have negligible mass) so a mol of Carbon-12 has a mass of 12 g.
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</details>
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## Thermal Expansion
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<details>
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<summary>
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### Origin of Thermal Expansion
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</summary>
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All atomic bonds vibrate, on the magnitude of gigahertz.
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The bonds vibrate about a mean positoin and the vibration is a simple harmonic motion.
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From the graph below you can see that as energy (in the form of heat) is supplied to the bonds,
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the amplitude of the vibrations get larger and larger.
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You can also see the mean position of the bond gets further and further away, meaning the volume
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of the material also is increasing.
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The mean position of the bond is what dictates the volume, as this means the inter-atomic
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separation increases.
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Morse potential is the energy well between 2 bonded atoms.
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The graph is asymmetric due to the repulsion experienced by atoms as they apporach.
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</details>
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### Linear Coefficient of Thermal Expansion
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$$\alpha_L = \frac{\Delta L}{L_0 \Delta T}$$
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where $L$ is the sample length.
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<details>
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<summary>
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#### Example 1
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A 1 m long bar of aluminium metal cools in the solid state from 660 \textdegree{}C to
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25 \textdegree{}C.
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Calculate the length of the bar after it cools down, given $\alpha_L = 25\times10^{-6}$ K$^{-1}$.
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</summary>
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\begin{align*}
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l_0 &= 1 \\
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\Delta T &= T_f - T_0 = 25 - 660 = -635 \\
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\\
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\alpha_L &= \frac{l_f - l_0}{l_0 \Delta T} \\
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\alpha_L l_0 \Delta T &= l_f - l_0 \\
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l_f &= \alpha_L l_0 \Delta T + l_0 = 0.984
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\end{align*}
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</details>
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### Linear Thermal Expansion and Isotropism
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Since isotropic solids have the same properties in all directions, you can say that for an
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isotropic solid:
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$$\alpha_V = 3\alpha_L = \frac{\Delta V}{V_0 \Delta T}$$
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### Reasons to Care About Thermal Expansion
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- A coating on a material may fail if the thermal expansion coefficients do not match
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- A brittle material may thermally shock and fracture due to thermal expansion mismatch between
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the ouside and inside, especially if the material is not very thermally conductive
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## Thermal Conductivity
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Thermal conductivity is the rate at which heat power is transferred through a material.
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$$\frac{Q}{A} = k \frac{\Delta T}{\Delta x}$$
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where $Q$ is heat power, $A$ is area of the surface, $\frac{\Delta T}{\Delta x}$ is the
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temperature gradient, and $k$ is the thermal conductivity constant.
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<details>
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<summary>
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### Origin of Thermal Conductivity
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</summary>
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Heat is transferred through materials by electrons (and partially by atomic vibrations)
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Metals have high thermal conductivity as their delocalised 'sea' electrons are about to move about
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easily.
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This makes them excellent conductors of heat and electricity.
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Ceramics, glasses, and polymers do not have delocalised electrons and are therefore poor conductors
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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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Lattice Parameter = 2r
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- Face centred cubic (FCC)
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- Body centred cubic (BCC)
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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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### 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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## 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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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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@@ -466,3 +466,41 @@ M_{OO} &= F_py_p = \int_{area}\! \rho gh^2 \,\mathrm{d}A \\
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\\
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y_p = \frac{M_{OO}}{F_p}
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\end{align*}
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## Buoyancy
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### Archimedes Principle
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> The resultant upwards force (buoyancy force) on a body wholly or partially immersed in a fluid is
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> equal to the weight of the displaced fluid.
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When an object is in equilibrium the forces acting on it balance.
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For a floating object, the upwards force equals the weight:
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$$mg = \rho Vg$$
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Where $\rho$ is the density of the fluid, and $V$ is the volume of displaced fluid.
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### Immersed Bodies
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As pressure increases with depth, the fluid exerts a resultant upward force on a body.
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There is no horizontal component of the buoyancy force because the vertiscal projection of the body
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is the same in both directions.
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### Rise, Sink, or Float?
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- $F_B = W$ \rightarrow equilirbrium (floating)
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- $F_B > W$ \rightarrow body rises
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- $F_B < W$ \rightarrow body sinks
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### Centre of Buoyancy
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Buoyancy force acts through the centre of gravity of the volume of fluid displaced.
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This is known as the centre of buoyancy.
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The centre of buoyancy does not in general correspond to the centre of gravity of the body.
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If the fluid density is constant the centre of gravity of the displaced fluid is at the centroid of
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the immersed volume.
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Reference in New Issue
Block a user