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8/8/2019 Nmc Exam Brush-up
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NMC EXAM BRUSH-UPNOVEMBER 2009
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Overview
1.Crystal Structures
2.Solidification and Crystal Defectsin Solids
3.Heat Treatments
4.Electrical Properties of Materials
5.Magnetic Properties of Materials
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CRYSTAL STRUCTURESChapter 3
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Crystal Structures
What do I need to know?Main Metallic Crystal
StructuresFCC, BCC, HCP, BCT
Polymorphism
Unit Lattices and BravaisLattices
Density Tool Box
Close-packed CrystalStructures
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Main Metallic Crystal Structures
BCC (-Fe , Na, Li and K)Coordination Number = 8
Effec tive numbe r o f ato ms = 2
Lattic e Parame ter a = 4R/3
Frac tio n o f Unit Ce ll that is o c c upie dby atoms by Volume
APF = Volume of Atoms/Volume of UnitCell
APF = 0.68
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Main Metallic Crystal Structures
FCC (-Fe, Au, Ag, Pt)Coordination Number = 12
Effec tive numbe r o f ato ms = 4
Lattic e Parame ter a = 4R/2
Frac tio n o f Unit Ce ll that is o c c upie dby atoms by Volume
APF = Volume of Atoms/Volume of UnitCell
APF = 0.74
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Main Metallic Crystal Structures
HCP ( , , ,C Cd Co Zn)Coordination Number = 12
Effec tive numbe r o f ato ms = 6
Lattic e Parame ter a = 2R & c =1.633a
Frac tio n o f Unit Ce ll that is o c c upie d
by atoms by VolumeAPF = Volume of Atoms/Volume of Unit
Cell
APF = 0.74
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Main Metallic Crystal Structures
Examples1.Calculate the radius of an iridium atom. Ir has
an FCC crystal structure and a density of22.4g/cm3 and an atomic weight of192.2g/mol (R = 0.136nm)
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Polymorphism
Crystal structure transformation inmaterials due to temperature orpressure change Fe
@ Room Temperature - BCC
Above 727C FCC
Above 1394C BCC
C @ Room Temperature HCP @ Very high pressures and temperatures
Diamond Cubic
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Unit and Bravais Lattices
14 Bravais lattices (RELAX you dont have toknow them all!)These include the geometrical shape of lattice
and atom placement
Cubic, Tetragonal, Hexagonal, Orthorhombic,Monoclinic, Rhombohedral and Triclinic
4 Types of unit lattices Only concerned with placement of atoms in lattice
Simple
Body-centred Face centered
End-centred
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Density Tool Box
Volumetric Density of Materials
v= (NR)(MR)/ [(Vcell )(NA)] ( /cm3) Planar Atomic Density
p= (N ( )R intersected atoms )/A plane( /toms mm2)Linear Atomic Density
l= (N ( )R atom diameters on line )/L line( / )toms mm
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Density Tool Box
Examples1.Consider the FCC crystal structure of Al.
Determine the planar atomic density of the(111) plane. (0.91)
2.Cobalt has an HCP crystal structure withan atomic radius of 0.1253nm and ac/a ratio of 1.623.
a)Compute the volume of the unit cell
for Co V = 0.0664nm3b)Explain in your own words why the
c/a ratio in question a is not equalto the theoretical value of 1.633.
3.
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Close-Packed Crystal Structures
FCC and HCP are both close-packed(APF 0.74)
Closely packed plane has the highest
planar densityPacking sequence differs
ABC ABC ABC FCC and AB AB AB HCP
FCC has more closely packed planes
than HCP and BCC does not have aclose packed plane
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Summary: Tips and Further Examples
Exam questions will most likely be morefocused on calculations than the theory ofthis chapter
Familiarise yourself with the sketches of FCC,
BCC, HCP and BCT If you can sketch it, CN, Atoms per unit
cell and APF can be UNDERSTOOD
Principle for Ionic crystals are similar just note
that the cation and anion valences HAVE TOBALANCE
Prove to yourself that the c/a ratio = 1.633 foran ideal HCP crystal
ALWAYS DRAW A PICTURE!!!
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IMPERFECTIONS IN SOLIDSChapter 4
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Crystal Structures
What do I need to know?Process of Solidification
Polycrystalline Metals (Sketch ingot
solidification mechanism)Single Crystals (Chozkralski process)
Defects in SolidsInfluencing factors
Types of Defects
Calculating Grain Size
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Process of Solidification
Heat is extracted from mold walls (high cooling rate, small grains)
Towards centre of ingot molten metal starts to cool (columnar zone)
Centre of ingot, last
metal solidifies (large equiaxed grains)
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Defects in Solids
Influencing Factors Mechanical Properties
Ductility
Electrical Properties Conductivity Heat conductivity ability
Diffusion of atoms Corrosion resistance
Types of Defects
( ,Microdefects point defects line defects and
)surface defects ( , ,Macrodefects Cracks pores inclusions and blow
)holes
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Defects in Solids
Microdefects Point Defects Vacancies
Nc = Ne(-Qv/kT)
Self-interstitial Defects
Impurities Most materials are used in alloy form
Simplest alloy is that of solid solution
Substitutional (Alloying atoms replaces thatof paremt atoms)
Interstitial (Alloying atoms positions betweenparent atoms)
Excess alloying elements above saturation limit two-phase solid
Solid solution also depends on Hume-Rothery
criteria
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Defects in Solids
Microdefects Point Defects Hume-Rothery Criteria
Rparent and Ralloy difference < 15%
Parent and alloy crystal structure must be
similar Electron negativity of 2 elements must be about
equal
2 Elements must have the same number ofvalence electrons
Schottky Defects (Ceramics) Missing cation AND anion
Frenkel Defects (Ceramics) Cation vacancy
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Defects in Solids
Formation of Point Defects Vacancies
During solidification
Rapid cooling
Cold work Radioactive bombardment
Self-interstitial Atoms Radioactive bombardment
Impurities
Solid solutions Diffusion of rogue species
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Defects in Solids
Microdefects Line defectsTwo primary types
Screw defects (Forms through shear)
Edge dislocation
-Positive dislocation
- Negative dislocation (Formation of Edge dislocations Usually forms
)through tension Solidification (Cold work Enhances slip of dislocations on
- )close packed planes Vacancy condensation
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Defects in Solids
Microdefects Surface defects Grain boundaries
Due to neighboring grains with differentgeometrical orientation
Grain boundary is area of high energy capacity
Always present in polycrystalline materials/alloys
Twinning Plane that has a mirror image
Forms through cold work (mechanical twins) orduring annealing (annealed twins)
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Defects in Solids
Macrodefects Cracks
Due to rapid cooling during solidification
Due to mechanical deformation
Pores or blow holes Due to decrease in gaseous solubility in the
molten metal, gas escapes through partiallysolidified surface
Inclusions
Rogue particles that intrude material duringmanufacturing
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Calculating Grain Size
N = 2n-1
N = Average number of grains per square inch(@100x)
n = Grain size number
Examples1.For an ASTM grain size of 6, how many grains
would there be per square inch at
a)100X? (32)
b)Without any magnification? (320 000)
2.Determine the ASTM grain size number if 25grains per square inch are measured at amagnification of 75. (4.8)
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Another Example
3.Calculate the fraction of atom sites that arevacant for Pbat its melting temperature of327C. Assume an energy for vacancyformation of 0.55eV/atoms. (2.41x10-5)
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Summary: Tips
This chapter contains mainly theory but theconcepts are of utter importance
Expect a few graphs in the exam on thischapter
Number of calculations in this chapter willprobably be limited
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HEAT TREATMENTChapter 9
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Heat Treatment
What do I need to know? Fe-C phase system
Interpretation of binary phase diagram
Phases present at specific temperature and
composition Lever-rule for calculating percentage of different
phases at temperatures and compositions
Phase transformations (peritectic, eutectic,eutectoid and peritectoid reactions)
Equilibrium phases and reactions Non-equilibruim phases
Heat treatments and microstructures
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Heat Treatment
Fe-C phase system
Only to be used forequilibrium coolingconditions
Phase diagram show
all of the reactions, compositions and
temperatures
Phases with
equilibrium cooling Ferrite, cementite
and pearlite
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Heat Treatment
Fe-C phase system Examples
1.By using the Fe-C phase diagram, answer thefollowing questions applicable to a 0.5%Chypoeutectoid steel that is cooled slowly
from 950C to just below 727C.a)Calculate the amount of proeutectoid ferrite in
the steel (38.71%)
b)Calculate the amounts of eutectoid ferrite andeutectoid cementite in the steel (54.17%and 7.1%)
c)
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Heat Treatment
Fe-C phase system Examples
2.Determine the chemical compositions of steelscontaining the following microstructuralcomponents after cooling
a)92% Ferrite and 8% Cementite (0.559%C)b)48.2% Proeutectoid ferrite (0.426% C)
c)4.7% Proeutectoid cementite (1.0773% C)
d)10.45% Eutectoid cementite (Hypereutectoid
composition) (1.388% C)e)
f)
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Heat Treatment
Non-equilibrium Phases Transformations Increase in cooling rate non-equilibrium
phases Bainite T from 250 550C
Fine dissemination of cementite in ferrite
matrix Good toughness, strength and hardness
properties Martensite Rapid cooling (quenching in water or
brine) C atoms dont have time to diffuse out of FCC
structure, are trapped in BCT cell Due to high amount of distortion associated
with phase transformation, hardness andstrength of martensite is very high
Temper treatment is often need to restoreductility of martensite
Tempering occurs below 650C and allows Cto precipitate out also known as
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Heat Treatment
Types of Treatments Annealing
Steel is austenitised, cooled at equilbriumcondictions
Large grains and coarse pearlite
Good ductility
Normarlising Air-quench
Finer grain size and pearlite
Harder component than annealed sample Hardening
Rapid queching in brine, oil, water or even liquidnitrogen
Martensite forms
Excessively high hardness
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Heat Treatment
Types of TreatmentsStress Relieftreatment
Cold worked, quenched, welded or machinedcomponents experience stress fluctuationsdue to internal stresses
Heat component below eutectoidtemperature to relieve internal stress
Spherodising Process at which componenet is heated to
allow the rediffusion of C atoms out of the
grains to form spheres) Good machinability and good ductility Spheres have the lowest surface to volume
energy therefore precipitates grow ingeometry to mimic this shape
a)
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Recap: Tips
You will most likely HAVE to use the lever ruleYou may expect some application type questions
If you have to design a heat treatment remember FITFOR PURPOSE
Cementite is highly brittle therefore any application
that requires good toughness, the amount in thematrix must be reduced propose spherodisingtreatment
With hypoeutectoid steels, pearlite can be a problemfor applications that require high strength CWcan resolve this to a degree
If a rapid quench (water, brine, oil or liquidnitrogen is proposed, you will propably endup with martensite tempering isessential)
Bainite can be produced by quenching in a molten Pbor salt bath and will give excellent mechanical
properties but time constraints have to be takeninto account
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ELECTRICAL PROPERTIES OF
MATERIALSChapter 14
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Electrical Properties of Materials
What do I need to know? Relationship between resistivity and
conductivity
3 Groups of electrical conductivity
Factors that influence resistivity andconductivity
Energy gap model for metals and isolators
Intrinsic semi-conductors
Extrinsic semi-conductors Dielectric character
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Electrical Properties of Materials
Resistivity and Conductivity Inversely proportional to each other
Resistance of material is dependent on the typeof material, length and cross-sectional area of
component Ohms law can be used to determine Resistance
and the micro-law can be used to determineconductivity or resistivity
3 Types of Conductors
Conductor (e.g. Metals with high conductivity) Semi-conductors (e.g. Si with moderate
conductivity)
Isolators (e.g. Ceramics with poor conductivity)
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Electrical Properties of Materials
Factors that influence resisitivityTemperature
Linear relationship between resistivity andtemperature
Purity of metal Alloying elements increase resistivity as electrons
have less mobility in the crystal structure
Crystal Defects An increase in the crystal defects will facilitate an
increase in the resistivity as they will form
barriers against the movement of electrons Resistivity can be reduced by heat treatments
(HX)
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Electrical Properties of Materials
Energy gap model Metals
Small amount of energy needed to fill energy gapwith metals
Therefore most metals have good conductivity
Isolators Energy gap is separated from a filled band and an
empty band
Electrons need a lot more energy to cross energygap therefore conductivity is lower
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Electrical Properties of Materials
Intrinsic Semi-Conductors (A-B-C) Pure, semi-conductors (Si and Ge)
Negative and positive electrons contribute to theconductivity of semi-conductors
With an increase in temperature , the
CONDUCTIVITY of the material increases forsemi-conductors since certain valence electronsare excited and their mobility increases
Extrinsic Semi-Conductors Differentiate between p- and n-type
Positive (Group 3 and 4 elements) and negativesemi-conductors (Group 4 and 5 elements)
By doping, impurities decrease the energy gapand through that, conductivity increases
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Electrical Properties of Materials
Extrinsic Semi-Conductors n-Type
Group 5 substitutes one of Group 4 atoms
Majority of conductors are electrons minority arevacancies
p-Type Group 3 replaces one of Group 4 atoms
Majority of conductors are vacancies minority areelectrons
Dielectric Character
Ceramics, ionics and some polymers mostlyisolators but in some cases also semi-conductors
Capacitor chambers
Pizo-electric ceramics Ceramics that can convert electrical pulses to
mechanical vibrations or vice versa
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MAGNETIC PROPERTIES OF
MATERIALSChapter 20
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Magnetic Properties of Materials
What do I need to know? Basic Principles (Theory)
Magnetic field strength and magnetic density
Relative permeabilities
Types of magnetism Diamagnetic, paramagnetic, ferromagnetic,
antiferromagnetic and ferrimagnetic
Influence of Temperature on Ferromagnetics
Hysteresis Magnetisation and demagnetisation and hysteris
loops
Differentitate between hard and soft magnetics
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Magnetic Properties of Materials
Types of MagnetismTypes of magnetism
Diamagnetic - r < 1
Paramagnetic particles move toward external
magnetic field but loses their magnetism whenfield is removed
Ferromagnetic Magnetisationcan be permanentdue to the half-filled orbital of elements. It isessential that electrons in the 3d orbital areunpaired
Antiferromagnetic Elements have a magneticmoment but the a/d ratio is does not rangebetween 1.4 and 2.7 no magnetism
Ferrimagnetism Traces magnetic moments usually ionic bonds- spine of electrons are anti-
parrallel but not magnetic
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Magnetic Properties of Materials
Influence of Temperature onFerromagnetics At the Curie temperature, the 3d-electrons
orientations changes and the parallel spin ofthe electrons decrease
At this temperature the ferromagnetic nature ofthe material is destroyed
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Magnetic Properties of Materials
Hysteresis Domains on atomic level can be altered via a
solenoid causes parallel movement of 3d-electrons
Magnetisation occurs with ferromagnetic andferrimagnetic materials due
Domains (which have the correct orientation) startto grow at the expense of incorrect orientateddomains
Incorrect orientated domains can be rotated if theapplied field strength is strong enough
Demagnetisation will occur if the material isheated above its Curie temperature, byapplying an opposite directed field strength
or increasing the dislocation density of thematerial
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Magnetic Properties of Materials
HysteresisSo-called hysteresis loop
shows the life-cycle of a
ferromagnetic materialThe larger the area of the
curve, the easier
magnetisation is possible
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Magnetic Properties of Materials
Hard VS Soft magnetics
HARD SOFT
High Hc and Br values Easy to magnetise anddemagnetise
Large negative magnetic fieldneed to demagnetise
Needs high Bs value and highpearmeability
Small magnetic field tomagnetise
Induced current due to themagnetic field
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Recap
The theory of this chapter is themost important since there arevery few types of calculations
that can be asked of youTypes of magnets is quite
important also the mechanism
that allows ferromagnetismB-H curve is very easy to
understand just follow yournotes