Heat Treatment - James Madison University
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Transcript Heat Treatment - James Madison University
Heat Treatment
ISAT 430
Heat Treatment
Three reasons for heat treatment
To soften before shaping
To relieve the effects of strain hardening
To acquire the desired strength and toughness
in the finished product.
Spring 2001
Dr. Ken Lewis
ISAT 430
Module 6
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Heat Treatment
Principal heat treatments
Annealing
Martensite formation in steel
Precipitation hardening
Surface hardening
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ISAT 430
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Annealing
Process
Heat the metal to a temperature
Hold at that temperature
Slowly cool
Purpose
Reduce hardness and brittleness
Alter the microstructure for a special property
Soften the metal for better machinability
Recrystallize cold worked (strain hardened) metals
Relieve induced residual stresses
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ISAT 430
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The Iron Carbon System
Steels, ferrous alloys, cast irons, cast steels
Versatile and ductile
Cheap
Irons (< 0.008% C)
Steels (< 2.11% C)
Cast irons (<6.67% [mostly <4.5%]C)
The material properties are more than composition –
they are dependent on how the material has been
treated.
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The
Phase
Diagram
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Fe - C
Iron melts at 1538°C
As it cools, it forms in sequence
Delta ferrite
Austenite
Alpha ferrite
Alpha ferrite
Solid solution of BCC iron
Maximum C solubility of 0.022% at 727°C
Soft and ductile
Magnetic up to the Curie temperature of 768°C
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Fe - C
Delta ferrite
exists only at high temperatures and is of little
engineering consequence.
Note that little carbon can be actually interstitially
dissolved in BCC iron
Significant amounts of Chromium (Cr), Manganese
(Mn), Nickel (Ni), Molybdenum (Mb), Tungsten (W),
and Silicon (Si) can be contained in iron in solid
solution.
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ISAT 430
Module 6
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Fe - C
Austenite (gamma iron)
Between 1394 and 912°C iron transforms from
the BCC to the FCC crystal structure.
It can accept carbon in its interstices up to
2.11%
Denser than ferrite, and the FCC phase is much
more formable at high temperatures.
Large amounts of Ni and Mn can be dissolved
into this phase
The phase is non-magnetic.
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Fe - C
Cementite
100% iron carbide Fe3C
Very hard
Very brittle
Pearlite
Mixture of ferrite and cementite
Formed in thin parallel plates
Bainite
Alternate mixture of the same phases
Needle like cementite regions
Formed by quick cooling
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Martensite formation in Steel
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The diagram at left
assumes slow equilibrium
cooling.
Each phase is allowed to
form
Time is not a variable.
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Martensite formation in Steel
Spring 2001
Dr. Ken Lewis
However
If cooling is rapid
enough that the
equilibrium reactions
do not occur
Austenite transforms
into a non-equilibrium
phase
Called Martensite.
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Fe - C
Martensite
Hard brittle phase
Iron carbon solution whose composition is the
same as austenite from which it was derived
But the FCC structure has been transformed
into a body center tetragonal (BCT)
The extreme hardness comes from the lattice
strain created by carbon atoms trapped in the
BCT
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The Time – Temperature – Transformation
Curve (TTT)
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The Time – Temperature – Transformation
Curve (TTT)
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Composition Specific
Here 0.8% carbon
At different compositions,
shape is different
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0.8C
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The Time – Temperature – Transformation
Curve (TTT)
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At slow cooling rates the
trajectory can pass through the
Pearlite and Bainite regions
Pearlite is formed by slow
cooling
Trajectory passes
through Ps above the
nose of the TTT curve
Bainite
Produced by rapid
cooling to a temperature
above Ms
Nose of cooling curve
avoided.
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The Time – Temperature – Transformation
Curve (TTT)
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If cooling is rapid enough
austenite is transformed into
Martensite.
FCC > BCT
Time dependent diffusion
separation of ferrite and
iron carbide is not
necessary
Transformation begins at Ms
and ends at Mf.
If cooling stopped it will
transition into bainite and
Martensite.
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Martensite hardness
Spring 2001
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ISAT 430
The extreme hardness
comes from the lattice
strain created by
carbon atoms trapped
in the BCT
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Tempered Martensite
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Step 1 -- Quench in the
martensitic phase
Step 2 – soak
Fine carbide particles
precipitate from the iron –
carbon solution
Gradually the structure
goes BCT > BCC
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Quenching Media
The fluid used for quenching the heated alloy effects
the hardenability.
Each fluid has its own thermal properties
Thermal conductivity
Specific heat
Heat of vaporization
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These cause rate of cooling differences
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Quenching Media2
Cooling capacities of typical quench media are
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Agitated brine
Still water
Still oil
Cold gas
Still air
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5.
1.
0.3
0.1
0.02
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Other quenching concerns
Fluid agitation
Renews the fluid presented to the part
Surface area to volume ratio
Vapor blankets
insulation
Environmental concerns
Fumes
Part corrosion
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Surface Hardening
Refers to a “thermo chemical” treatment whereby
the surface is altered by the addition of carbon,
nitrogen, or other elements.
Sometimes called CASE HARDENING.
Commonly applied to low carbon steels
Get a hard wear resistant shell
Tough inner core
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Surface Hardening2
The common procedures are:
Carburizing
Nitriding
Carbonnitriding
Chromizing and boronizing
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Carburizing
Heating a low carbon steel in the presence of carbon rich
environment at temperature ~ 900°C
Carbon diffuses into the surface
End up with a high carbon steel surface.
Pack parts in a compartment with coke or charcoal
Gas carburizing
Uses propane (C3H8) in a sealed furnace
Liquid carburizing
Used NaCN, BaCl2
Thickness 0.005 in. to 0.030 in.
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Nitriding
Nitrogen is diffused in the surface of special alloy
steels at temperatures around ~510°C.
Steel must contain elements that will form nitride
compounds.
Aluminum
Chromium
Forms a thin hard case without quenching
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Thicknesses 0.001 in – 0.020 in.
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Chromizing
Diffuse chromium into the surface 0.001 – 0.002 in.
Pack the parts in Cr rich powders or dip in a molten
salt bath containing Cr salts.
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Boronizing
Performed on tool steels, nickel and cobalt based
alloy steels.
When used on low carbon steels, corrosion
resistance is improved.
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