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UNIT 4

PHYSICAL METALLURGY

OP Jindal Institute of Technology

Babbitt metal Babbitt, also called Babbitt metal or bearing metal, is an alloy used for the bearing surface in a plain bearing. Babbitt metal is most commonly used in as a thin surface layer in a complex, multi-metal structure, but its original use was as a cast-in-place bulk bearing material. Babbitt metal is characterized by its resistance to galling. Babbitt metal is soft and easily damaged, which suggests that it might be unsuitable for a bearing surface. However, its structure is made up of small hard crystals dispersed in a softer metal, which makes it a metal matrix composite. As the bearing wears, the softer metal erodes somewhat, which creates paths for lubricant between the hard high spots that provide the actual bearing surface.
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

When tin is used as the softer metal, friction causes the tin to melt and function as a lubricant, which protects the bearing from wear when other lubricants are absent. There are many Babbitt alloys in addition to Babbitt's original. Some common compositions are: 90% tin, 10% copper 89% tin, 7% antimony, 4% copper 80% lead, 15% antimony, 5% tin 75% lead, 10% tin 76% copper, 24% lead 67% copper, 28% tin, 5% lead
Galling usually refers to adhesive wear and transfer of material between metallic surfaces during sheet metal forming and other industrial applications where relative motion are involved
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Phase Transformations in Metals

Goal: obtain specific microstructures to improve mechanical properties of a metal.


Heat Treatment (time and temperature) Microstructure Mechanical Properties Kinetics of phase transformations Multiphase Transformations Phase transformations in Fe-C alloys Isothermal Transformation Diagrams Mechanical Behavior Tempered Martensite
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Phase transformations: Kinetics

(Kinetics time dependence) Transformations do not occur instantaneously

Three categories
Diffusion-dependent with no change in composition or number of phases present (melting/solidification of pure metal, allotropic transformations, recrystallization) Diffusion-dependent but changes in composition or number of phase (eutectoid transformations) Diffusionless metastable phase by small displacements of atoms in structure
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Superheating / supercooling Crossing phase boundary new equilibrium state Takes time transformation is delayed During cooling, transformations occur at temperatures less than predicted by phase diagram: supercooling. During heating, transformations occur at temperatures greater than predicted by phase diagram: superheating. Degree of supercooling/superheating increases with rate of cooling/heating. Microstructure is strongly affected by the rate of cooling.
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Isothermal Transformation (or TTT) Diagrams (Temperature, Time, and % Transformation)

Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

TTT Diagrams

Thickness of ferrite and cementite layers in pearlite is ~ 8:1. Absolute layer thickness depends on temperature of transformation.
Higher temperature thicker layers.
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Family of S-shaped curves at different T Isothermal (constant T) transformation material is cooled quickly to T THEN transformation occurs) Low T Transformation occurs sooner (controlled by rate of nucleation). Grain growth reduced (controlled by diffusion)

Slow diffusion leads to fine grains + thin - layers (fine pearlite)


High T diffusion rates allow for larger grain growth + formation of thick layers (coarse pearlite) Compositions other than eutectoid, proeutectoid phase (ferrite or cementite) coexists with pearlite.
Dr. Ashok Kumar Srivastava

Formation of Bainite Microstructure (I)


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Transformation T enough (540C)

low

Bainite rather than fine pearlite forms

Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Formation of Bainite Microstructure (II)


T ~ 300-540C, upper bainite consists of needles of ferrite separated by long cementite particles T ~ 200-300C, lower bainite has thin plates of ferrite and fine rods or blades of cementite Bainite: transformation rate controlled by microstructure growth (diffusion) rather than nucleation. Diffusion is slow at low T, It has a very fine (microscopic) microstructure. Pearlite and bainite transformations are competitive.
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Upper bainite

Lower bainite

Dr. Ashok Kumar Srivastava

Spheroidite
OP Jindal Institute of Technology

Annealing of pearlitic or bainitic at T just below eutectoid (e.g. 24h at 700C) forms spheroidite - Spheres of cementite in a ferrite matrix. Relative amounts of ferrite and cementite do not change, only shape of cementite inclusions changes Transformation proceeds by C diffusion needs high T. Driving force reduction in total ferrite - cementite boundary area

Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Martensite (I) Martensite:austenite quenched to room T Nearly instantaneous at required T Austenite martensite does not involve diffusion no activation: athermal transformation Each atom displaces small (sub-atomic) distance to transform FCC -Fe (austenite) to martensite, a Body Centered Tetragonal (BCT) unit cell (like BCC, but one unit cell axis longer than other two) Martensite is metastable - persists indefinitely at room T: transforms to equilibrium phases on at elevated temperature Martensite can coexist with other phases and microstructures Since martensite is a metastable phase, it does not appear in phase Fe-C phase diagram.
Dr. Ashok Kumar Srivastava

TTT Diagram including Martensite


OP Jindal Institute of Technology

Austenite-to-martensite is diffusionless and fast. Amount of martensite depends on T only.

Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Time-temperature path microstructure

Dr. Ashok Kumar Srivastava

Mechanical Behavior of Fe-C Alloys (I)


OP Jindal Institute of Technology

Cementite is harder and more brittle than ferrite increasing cementite fraction makes harder, less ductile material.

Dr. Ashok Kumar Srivastava

Mechanical Behavior of Fe-C Alloys (II)


OP Jindal Institute of Technology

Strength and hardness inversely related to the size of microstructures (fine structures have more phase boundaries inhibiting dislocation motion).

Bainite, pearlite, spheroidite


Considering microstructure we can predict that Spheroidite is softest Fine pearlite harder + stronger than coarse pearlite Bainite is harder and stronger than pearlite

Martensite
Of the various microstructures in steel alloys Martensite is the hardest, strongest BUT most brittle
Dr. Ashok Kumar Srivastava

Mechanical Behavior of Fe-C Alloys (III)

OP Jindal Institute of Technology

Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Tempered Martensite (I) Martensite is so brittle it needs to be modified for practical applications. Done by heating to 250-650oC for some time: (tempering)

tempered martensite, extremely fine-grained, well dispersed cementite grains in a ferrite matrix.
Tempered martensite is more ductile Mechanical properties depend upon cementite particle size: fewer, larger particles means less boundary area and softer, more ductile material - eventual limit is spheroidite. Particle size increases with higher tempering temperature and/or longer time (more C diffusion).
Dr. Ashok Kumar Srivastava

OP Jindal Institute of Technology

Tempered Martensite (II)


Higher temperature & time: spheroidite (soft)

Electron micrograph of tempered martensite


Dr. Ashok Kumar Srivastava

Summary of austenite transformations


Austenite

OP Jindal Institute of Technology

Slow cooling

Rapid quench

Moderate cooling

Solid lines are diffusional transformations, dashed is diffusionless martensitic transformation

Pearlite ( + Fe3C) + a proeutectoid phase

Bainite ( + Fe3C)
Reheat

Tempered martensite ( + Fe3C)


Dr. Ashok Kumar Srivastava

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