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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