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Schottky defects
When two oppositely charged ions are missing from an ionic crystal, action-anion divacancy is created which is
known as schottky imperfection.
Frenkel defects
If a positive cation moves into an interstitial site in an ionic crystal, a cation vacancy is created in the normal
ion site. This vacancy-interstitialcy pair is called the Frenkel imperfection.
Screw dislocation
A screw dislocation is much harder to visualize. Imagine cutting a crystal along a plane and slipping one half across
the other by a lattice vector, the halves will fit back together without leaving a defect. If the cut only goes part way
through the crystal, and then slipped, the boundary of the cut is a screw dislocation. Despite the difficulty in
visualization, the stresses caused by a screw dislocation are less complex than those of an edge dislocation. These
stresses need only one equation, as symmetry allows only one radial coordinate to be used: [1]
Where μ is the shear modulus of the material, b is the Burgers vector, and r is a radial coordinate. This equation
suggests a long cylinder of stress radiating outward from the cylinder and decreasing with distance. Please note, this
simple model results in an infinite value for the core of the dislocation at r=0 and so it is only valid for stresses
outside of the core of the dislocation.[1]
Edge dislocation
An edge dislocation is a defect where an extra half-plane of atoms is introduced mid way through the crystal,
distorting nearby planes of atoms. When enough force is applied from one side of the crystal structure, this extra
plane passes through planes of atoms breaking and joining bonds with them until it reaches the grain boundary. A
simple schematic diagram of such atomic planes can be used to illustrate lattice defects such as dislocations. (Figure
B represents the "extra half-plane" concept of an edge type dislocation).
The stresses caused by an edge dislocation are complex due to its inherent asymmetry. These stresses are described
by three equations: [1]
The Burgers vector, often denoted by b, is a vector that represents the magnitude and direction of the lattice
distortion of dislocation in a crystal lattice.[1]
The direction of the vector depends on the plane of dislocation, which is usually on the closest-packed plane of unit
cell. The magnitude is usually represented by equation:
Where a is the unit cell length of the crystal, ||b|| is the magnitude of Burgers vector and h, k, and l are the
components of Burgers vector, b = <h k l>. In most metallic materials, the magnitude of the Burgers vector for a
dislocation is of a magnitude equal to the interatomic spacing of the material, since a single dislocation will offset
the crystal lattice by one close-packed crystallographic spacing unit.
In edge dislocations, the Burgers vector and dislocation line are at right angles to one another. In screw
dislocations, they are parallel.
The Burgers Vector is significant in determining the strength of a material: it affects solute hardening, precipitation
hardening and work hardening, all of which affect yield strength.
Diffusion Mechanisms
Diffusion describes the spread of particles through random motion from regions of higher concentration to regions
of lower concentration.
Kirkendal effect
Ernest Kirkendall reported the results of experiments on the inter diffusion between copper and zinc in brass and
observed the movement of the interface between the different phases due to high-temperature inter diffusion, now
called the Kirkendall Effect.
Today, the effect has been taken into account in various fields in materials science and technology such as
structural materials welding, metals and ceramics powders sintering, thin films, and large-scale integration.
(OR)
In binary solution, two different elements, rate at which they diffuse are not necessarily equal. Usually, the lower
melting component diffuses much faster than the other. If an inert marker (say, thin rod of a high melting point
substance which is insoluble in the diffusion matrix) is placed at the weld joint of the couple, prior to the diffusion
anneal, the marker is found to shifting during annealing in the same direction as the slower moving species. This
phenomenon is termed as Kirkendall effect.
Invariant reaction
In a binary (component, C=2) phase diagram, If three phases (P=3) coexist then the degree of freedom (F) at
the point is zero (F=C-P+1 => F=2-3+1 => F=0). The degree of freedom zero means this can occur only at a
particular temperature and particular composition and the point in the phase diagram is known as the
invariant point. Any reaction or transaction occurred at that point is termed as invariant reaction.
Phase
A phase in a material in terms of its micro-structure is a region that differs in structure and or composition
from another region.
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In thermodynamics a chemically and physically uniform quantity of matter that can be separated mechanically from
a non homogeneous mixture. It may consist of a single substance or of a mixture of substances. The three basic
phases of matter are solid, liquid, and gas; other phases that are considered to exist include crystalline (see crystal),
colloidal (see colloid), glass, amorphous, and plasma. The different phases of a pure substance are related to each
other in terms of temperature and pressure. For example, if the temperature of a solid is raised enough, or the
pressure is reduced enough, it will become a liquid.
Phase diagram
A phase diagram in physical chemistry, engineering, mineralogy, and materials science is a type of chart used to
show conditions at which thermodynamically-distinct phases can occur at equilibrium. In mathematics and physics,
"phase diagram" is used with a different meaning: a synonym for a phase space.
Overview
Common components of a phase diagram are lines of equilibrium or phase boundaries, which refer to lines that
mark conditions under which multiple phases can coexist at equilibrium. Phase transitions occur along lines of
equilibrium.
1. 2D phase diagrams
2. 3D phase diagrams :
Other much more complex types of phase diagrams can be constructed, particularly when more than one pure
component is present. In that case concentration becomes an important variable. Phase diagrams with more than
two dimensions can be constructed that show the effect of more than two variables on the phase of a substance.
Polymorphic and polyamorphic substances have multiple crystal or amorphous phases, which can be graphed in
a similar fashion to solid, liquid, and gas phases.
In liquid crystal physics, phase diagrams are used in the case of mixing of nematogenic compounds to
distinguish between the isotropic liquid phase, the nematic liquid phase.
Lever rule
Using the lever rule one can determine quantitatively the relative composition of a mixture in a two-phase region in
a phase diagram. The distances l from the mixture point along a horizontal tie line to both phase boundaries give the
composition: [1]
Where:
• represents the amount of phase α
• Represents the amount of phase β.
• It can be conveniently expressed as: [2]
%α = (x * L) / (α * L) * 100
%L = (α * x) / (α * L) * 100
Tensile strength
Ultimate tensile strength (UTS), often shortened to tensile strength (TS) or ultimate strength,[1][2] is the maximum
stress that a material withstand before necking. The UTS is usually found by performing a tensile test and recording
the stress versus strain; the highest point of the stress-strain curve is the UTS. It is an intensive property, therefore
its value does not depend on the size of the test specimen. However, it is dependent on other factors, such as the
preparation of the specimen and the temperature of the test environment and material.
(Or simply)
The strength of material expressed as the greatest longitudinal stress it can bear without tearing apart,
Engineering stress
The stress , or intensity of internal forces, can be obtained by dividing the total normal force , determined from
the equilibrium of forces, by the cross-sectional area of the prism it is acting upon. The normal force can be a
tensile force if acting outward from the plane, or compressive force if acting inward to the plane. In the case of a
prismatic bar axially loaded, the stress is represented by a scalar called engineering stress or nominal stress that
represents an average stress ( ) over the area, meaning that the stress in the cross section is uniformly
distributed. Thus, we have
Engineering strain
The (Cauchy strain or) engineering strain is expressed as the ratio of total deformation to the initial dimension of
the material body in which the forces are being applied. The engineering normal strain or engineering extensional
strain e of a material line element or fiber axially loaded is expressed as the change in length ΔL per unit of the
original length L of the line element or fibers. The normal strain is positive if the material fibers are stretched or
negative if they are compressed. Thus, we have
Where is the engineering normal strain, L is the original length of the fiber and is the final length of the fiber.
The engineering shear strain is defined as the change in the angle between two material line elements initially
perpendicular to each other in the no deformed or initial configuration.
True stress
Engineering stress is Force / prime (early) Area = F/A0
True stress is Force / Area in any time = F/A
engineering strain is (Lf-L0)/L0 while Lf is length of sample after deformation and L0 is early length of sample
(before deformation)
True stress is defined is d (Epsilon) = dL/L therefore
Epsilon = ln (Lf/L0).
Therefore: True Stress = Eng. Stress X (1+Eng. Strain)
and True Strain = ln(1+Eng. Strain)
True strain
The logarithmic strain ε, also called natural strain, true strain or Hencky strain. Considering an incremental strain
(Ludwik)
Where e is the engineering strain. The logarithmic strain provides the correct measure of the final strain when
deformation takes place in a series of increments, taking into account the influence of the strain path.[2]
Shear strain
The engineering shear strain is defined as the change in angle between two originally orthogonal material lines. In
the figure above, the engineering shear strain (γxy) is the change in angle between lines and . Therefore,
The tonsorial shear strain components of the infinitesimal strain tensor can then be expressed using the engineering
strain definition, , as
Shear strain
Expressed in (SI unit): 1, or radian
Commonly used symbols: γ or ϵ
Expressed in other quantities: γ=τ/G
Modulus elasticity
Modulus of elasticity, also known as elastic modulus or Young’s Modulus, is a measure of how a material or
structure will deform and strain when placed under stress. Materials deform differently when loads and stresses are
applied, and the relationship between stress and strain typically varies. The ability of matter to resist or transmit
stress is important, and this property is often used to determine if a particular material is suitable for a specific
purpose.
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When a material is subjected to an external load it becomes distorted or strained. With metals, provided the
loading is not too great, they return to their original dimensions when the load is removed, i.e. they are
elastic. Within the limits of elasticity, the ratio of the linear stress to the linear strain is termed the modulus of
elasticity or more commonly known as Young's Modulus.
Yield strength
The yield strength or yield point of a material is defined in engineering and materials science as the stress at which
a material begins to deform plastically. Prior to the yield point the material will deform elastically and will return to
its original shape when the applied stress is removed. Once the yield point is passed some fraction of the
deformation will be permanent and non-reversible.
In the three-dimensional space of the principal stresses (σ1,σ2,σ3), an infinite number of yield points form together a
yield surface.
Knowledge of the yield point is vital when designing a component since it generally represents an upper limit to the
load that can be applied. It is also important for the control of many materials production techniques such as
forging, rolling, or pressing. In structural engineering, this is a soft failure mode which does not normally cause
catastrophic failure or ultimate failure unless it accelerates buckling.
Resilience
Resilience is the property of a material to absorb energy when it is deformed elastically and then, upon unloading to
have this energy recovered. In other words, it is the maximum energy per unit volume that can be elastically stored.
It is represented by the area under the curve in the elastic region in the Stress-Strain diagram.
Modulus of Resilience, Ur, can be calculated using the following formula: ,
where σ is yield stress, E is Young's modulus, and ε is strain.
Elastic behavior
C. Hookian behavior:
σ d = Eε
E = σ d /ε
3. Large E = stiff rocks, requires large amounts of stress to obtain a certain amount of strain
Group B