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Structures and Properties of Metallic Materials Ceramics Polymers Composites Encompasses - Electronic, Magnetic, Optical, Mechanical, and Chemical Properties FE/EIT Exam - Two Major Areas - Fundamentals of
1. Strength, Deformation, Plasticity of Crystalline Solids 1 2. Phase Equilibrium in Metallic Systems
Tension Testing
Two distinct stages of deformation Elastic Deformation (Reversible Change in Volume) Plastic Deformation (Irreversible Constant Volume) Elastic Deformation
Hookes Law s = Ee
s = Stress
e = Strain
Figure 3.1
Fracture Stress = sf
Ductility Figure 3.2
Plastic deformation involves sliding of atomic planes called slip deformation, analogous to shear.
Slip System - Combination of a close-packed plane and a close-packed direction. Slip occurs along planes and are restricted in crystallographic directions that are the most densely packed. The greater the planes and directions, the easier it is to produce plastic slip without brittle fracture.
Slip Deformation -
continued
Dislocation Edges (tRcrit < 1/5 Theoretical) Figure 3.7-8 Dislocation Lines & Frank-Reed Source
Figure 3.9
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Compressive Strength
Compressive Stress similar to Tensile Stress (except no necking in pure compression) quite useful for materials which are brittle in tension, but have significant compressive load bearing capabilities (concrete, cast iron, etc).
Hardness Test
Determines resistance to penetration of a stylus. Useful for qualitative estimate of service wear, strength, and toughness. Brinell, Rockwell, Vickers, MicroHardness Table 3.1
Fatigue Test
Cyclic Load - Fatigue Life Number of Cycles (N) to Failure with Cyclic Stress Amplitude (S)
Fatigue Testing -
continued
Fatigue fractures are progressive. Fatigue Strength Maximum Cyclic Stress Amplitude for a specified number of cycles until failure. Fatigue is a surface active failure. Surface defect (notch) can initiate crack. Rough surface reduces fatigue strength by 25%. Cold rolling/shot peening increases by 25%. Corrosive Fatigue important cause of service failure.
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Fatigue Testing -
continued
Fatigue Life / Fatigue Strength improved by Highly Polished Surface Surface Hardening Carburizing, Nitriding, etc. Surface Compression Stresses Shot Peening, Cold Rolling, etc.
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e = e0(1 + bt 1/3)e kt
t = Time
Figure 3.13
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e = Strain
Metallurgical Variables
Microstructural Conditions Effects of Heat Treatment Effects of Processing Variables Effects of Service Conditions
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Microstructural Conditions
Grain Size Effect Ordinary temperature - fine grain, more strength High temperature - larger grain, greater strength Single Phase vs Multiphase Alloys Second phases many add profound differences Porosity & Inclusions - Poor mechanical properties Directionality Rolling direction vs transverse direction affect mechanical properties, introduce anisotropy
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Flame Cutting - Drastic changes of microstructure near the flame-cut surface, affects properties.
Machining and Grinding - Cold working results in stain hardening, may produce surface cracks.
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Equilibrium
Equilibrium between Phases Gibbs Phase Rule P + F = C + 2 P = number of phases, C = number of elements F = degrees of freedom, 2 = external variables (temperature and pressure).
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Eutectics
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Ionic Bonding
Electropositive and Electronegative Elements Example: Due to exchanged electrons Sodium (Na+) and Chlorine (Cl-) Opposite charges attract Figure 3.26 Electron clouds repel Potential energy minimum at balance distance Potential Well = Preferred Site Figure 3.27
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Covalent Bonding
Homopolar (Covalent) Bonding = Electron Sharing Bonding Pairs = Number of Shared Electrons = 8 - N ( N=Valence) Carbon (Atomic Number 6) Electron Configuration 1(s)22(s)22(p)2 Valence Electrons = 2 (from 2s) + 2 (from 2p) = 4 Bonding Pairs = 8 - 4 = 4
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Metallic Bonding
Metallic Elements (Valence = 1 or 2) Valence Electrons free to migrate and are not localized to individual atoms in as in the case of ionic or covalent bonding. The sea of migrating electrons and the attraction between positively charged atoms producing threedimensional periodic lattices.
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Electrical Properties
Ionic and Covalent Bonding Localized Electrons = Insulators Conductivity increases with temperature
Metallic Bonding Free Migrating Electrons Collide with Oscillating Lattices Higher Mean Free Path = Higher Conductivity Conductivity decreases with temperature
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Energy Bands
Paulis Exclusion Principle (2 per state) Energy bands have quasi-continuous levels Fill from lowest to highest energy levels Additional energy (thermal or electric field) Kinetic energy increases Electrons move up an energy level Figure 3.28 but only at the highest level Conduction Band - Valence Band - Energy Gap Semiconductors 31 Energy Gap
Figure 3.37
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Miller Indices
System of notation used for denoting planes and directions in crystalline structures (hkl). Note: All integers, without common factors.
Figure 3.38
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Primitive Cells
Only Corner Atoms Cubic Lattice, Hexagonal Lattice BCC, FCC, HCP are not primitive cells. Number of Atoms per Cell Simple Cubic (1/8 * 8) = 1 per cell FCC (1/8 * 8 + 1/2 * 6) = 4 per cell BCC (1/* * * + 1) = 2 per cell
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Interplaner Spacing
Interplaner Distance (dhkl) Figure 3.39 Perpendicular distance between equivalent planes Measured in Angstrom Units A = 10-8 cm Atomic Packing Factor = Volume of Atoms Volume of Space FCC APF = 0.74V Figure 3.40 BCC APF = 0.68 Figure 3.41 X-Ray Crystallography Braggs Law 2dhkl = sin q = h g 36 g is X-Ray Wavelength and h is Reflection Number