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MATERIAL SCIENCE LAB IIIRD
SEM, B.TECH
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DEPARTMENT OF MECHANICAL ENGINEERING
EXPERIMENTNO:
OBJECT: To study of hardening of steel and effect of quenching medium on hardness.
THEORY: Hardening of steel
Hardening of steel is obtained by a suitable quench within or above the critical range. The
temperatures are the same as those given for full annealing. The soaking time in air furnaces
should be 1,2 min for each mm of cross-section or 0,6 min in salt or lead baths. Unevenheating, overheating and excessive scaling should be avoided. The quenching is necessary to
suppress the normal breakdown of austenite into ferrite and cementite, and to cause a partial
decomposition at such a low temperature to produce martensite.to obtain this, steel requires
a critical cooling velocity, which is greatly reduced by the presence of alloying elements,
which therefore cause hardening with mild quenching. The quenching is necessary to supress
the normal breakdown of austenite into ferrite and cementite, and to cause a partial
decomposition at such a low temperature to produce martensite. To obtain this ,steel requires
a critical cooling velocity ,which is greatly reduced by the presence of alloying elements,
which therefore cause hardening with mild quenching(e.g. oil and hardening steels). Steels
wit less than o,3% carbon cannot be hardened effectively,while the maximum effect is
obtained at about 0,7% due to an increased tendency to retain austenite in high carbon steels.
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Fig.1. Variation of hardness of martensite and bainite with carbon content
Water is one of the most efficient quenching media where maximum hardness is
required,but it is liable to cause distortion and cracking of the article.Where hardness can be
sacrificed,whale,cotton seed and mineral are used.These tend to oxidise and form sludge
with consequent lowering of efficiency.The quenching velocity of oil is much less than
water.Ferrite and troostite are formed even in small sections.Intermidiate rates between
water and oil can be obtained with water containing 10-30% Ucon,a substance with an
inverse solubility which therefore deposits on the object to slow the rate of cooling.to
minimise distortion,long cylindrical object should be quenched vertically,flat sections
edgesways and thick sections should enter the bath first.To prevent steam bubbles forming
soft spots ,a water quenching bath should be agitated.
Full hardened and tempered steels develop the best combinations of strength and non-
ductility.
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Tampering & toughening
The martensite of quenched tool steel is exceedingly brittle and highly stressed.Consequently
cracking and distortion of the object are liable to occur after quenching.Retained ausentite is
unstable and as it changes dimensions may after,e.g.dies may alter0,012 mm. It is
necessary,therefore,to warm the steel below the critical range in order to relieve stresses and
to allow the arrested reaction of cementite precipitaions to take place.This is known as
tempering.
150-250C.The object is heated in an oil bath, immediately after quenching, to preventrelative cracking, to relieve internal stress and to decompose austentite without muchsoftening.
200-450C. Used to toughen the steel at the expense of hardness. Brinell hardnessnumber is 350-450.
450-700C. The precipitated cementite coalesces into larger masses and the steelbecomes softer. The structure is known as sorbote, which at the higher temperatures
becomes coarsely spheroidised. It itches more slowly than troostite and has a brinell
hardness number 220-350. Sorbite is generally found in heat-treated constructional steels,
such as axels, shafts, crankshafts subjected to dynamic stresses. A treatment of quenching
and tempering in this temperature range is frequently referred to as toughening, and it
produces an increase in ratio of the elastic limit to the ultimate tensile strength.
The reactions in tempering occur slowly. Reaction time as well as temperature of heating
is important. Tempering is carried to an extend under pyrometric control in oil, salt (e.g
equal parts of sodium and potassium nitrates for 200C-600C) or lead baths and also in
furnaces in which the air is circulated by fans. After the tempering, the objects may be
cooled either rapidly or slowly, except for steels susceptible to temper britellness.
Temper colours formed on a cleaned surface still used occasionally as a guide totemperature. They exists due to the interference effects of thin films of oxides formed
during tempering , and they act similarly to oil films on water.
Alloys such as stainless steel forms thinner films than do carbon steels for a given
temperature and hence produce a colour lower in the series. For example, pale straw
corresponds to 300C, instead of 230C(table 1)
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Temper colour Temperature C Objects
Pale straw 230 Planning and slotting tools
Dark straw 240 Milling cutters and drills
Brown 250 Taps, shear blades for metals
Brownish-purple 260 Punches, cups, snaps, twist drills,reamers
Purple 270 Press tools, axes
Dark purple 280 Cold chisels, sets for steel
Blue 300 Saws for wood, springs
Blue 450-650 Toughening for constructional steels
For turning , planning , shaping tools and chisels , only the cutting parts need hardening. This is
frequently carried out in engineering works by heating the tool to 730C, followed by quenching
and cutting end vertically. When the cutting end gets cold, it is cleaned with stone and the heat
from the shank of the tool is allowed to temper the cutting edge to the correct colour . Then the
whole tool is quenched. Oxidation can be reduced by coating the tool with charcoal and oil.
Changes during tempering
the principles underlying the tempering of quenched steels have a close similarity to those of
precipitation hardening. The overlapping changes, which occur when high carbon martenstite is
tempered , are shown in fig.2 and as follows:-
Stage 1: 50-200C. martenstie breaks down to a transition precipitate known as c-carbide(Fe2,4C) across twins and a low cabon martenstie which results in slight dispersion
hardening , decrease in volume and electrical resistance.
Stage 2. 205-305C. decomposition of retained austenite to bainite and decrease inhardness.
Stage 3.250-500C. conversion of aggregate of low carbon martensite and c-carbide intoferrite and cementite precipitated along twins, which gradually coarsens to give visible
particles and rapid softening ,Fig .3.
Stage 4.carbide changes in alloy steel at 400-700C. In steels containing one alloyingaddition, cementite forms first and the alloy diffuses to it. When sufficiently enriched the
Fe3C transforms to an alloy carbide. After further enrichment this carbide may be
superseded by another and this formation of transition carbides may be repeated several
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times before the equilibrium carbide forms. In the chromium steel, changes are :Fe3C
>Cr7C3>Cr23C6. In steels containing several carbide forming elements the reaction
are often more complex, and the carbides which decompose are not necessary followed
by carbides based on the same alloy elements. The transformation can also occur in
suitable gradual exchange of atoms without any appreciable hardening; or by resolution
of existing iron carbides and fresh nucleation of coherent carbide with considerable
hardening that counteracts the normal softening that occurs during tempering. In some
alloy steels, therefore, the hardness is maintained constant up to about 50000C or in some
cases it rises to a peak followed by a gradual drop due to breakdown of coherance of the
cabide particles. This agehardenning process is known as secondary hardening and it
enhances high temperature creep properties of steel ( e.g. steel E in fig.2). Chromium,for
a example, seems to stabalise the size of the cementite particles over a range 200-5000C.
vanadium and molybdenum form a fine dispersion of coherant precipitates (V4C3Mo2C)
in a ferrite matrix with conciderable hardening. When overr-ageing starts the V4C3 grows
in the grain boundaries and also forms a Widmansttten pattern of plates within the grain.
Figure 2. Tempering curves for 0.35% C steel and die steel
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a) As quenched. Laths with high density of dislocation.b) Tempered 300C. Widmanattten precipitation of carbides within laths.c) Tempered 500C. Recovery of dislocation structure into cells with laths.d) Tempered 600C. Recrystallisation cementite rebucleatedequioxed ferrite boundaries.e) High C twinned martensite.f) Tempered 100C. fine e-carbides across twins.g) Tempered 200C. coherant cementite along twins, c-carbides dissolve.h) Tempered 4000C. breakdown of twinned sstructure. Carbides grow and spheroidise.Figure 3. Low cardon lath martensites have a high Ms temperature and some tempering oftenoccurs on cooling, i.e. autotempering.
Quenching:-
The quenching and partitioning process has been developed to produce high strength steel.
After austenitisation and interrupted quinching and austanite transforms parrtly to martensite.
The remaining austantite is stablised by carbon partitioning from martensite. After final
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MATERIAL SCIENCE LAB IIIRD
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quench the tampered martasite gives a high strength level. The TRIP-assisted local strain
hardening assures satisfying dutility. The process desingh is limited by reactions competing
against the carbon partitioning, i.e. carbon precipitation and isothermal bainite transfomation.
For a given chemical composition a vast scope of adjustable mechanical properties are
investigated as a function of a process perameters. The corresponding micro structure is
characterised by light and electron microscopy and XRD measurements. Suplimentary
information on the process kinetics is obtained by dilatometry. Silicon shows more effective
in retarding cementite precipitation than aluminium. Retained austenite occurs in filmy
constitution between bcc laths as well as blocky grains.
Quenching:- It is the process of rapidly cooling the metal from the solution or austenitizing
treating temperature, typically from within the range of 815C 1100C (1500F to 2012F) for
steel. High-alloy and stainless steel may be quenched to minimise grain bour dary carbides or to
improve the ferrite distribution but most steel including carbon, low-alloy, and tool steel, are
quenched to produce controlled amounts of martensite in the micristructure. Successful
hardenind usually means achieving the required microstructure, hardness, or toughness while
minimizing residual stress, distortion, and the possibility of cracking.
The a quench medium is usually a liquid such as water and depends on the harden-ability of the
particular alloy, the section thickness and shape involved, and the cooling rates needed toachieve the desired microstructure. The most common quenchmedia are either liquid or gases.
The liquid quench commonly used include:
Oil that may contain a variety of additives Leceted liquid polymers Water that may contain salt or caustic additives
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DEPARTMENT OF MECHANICAL ENGINEERING
Gas type quench medians may also be used, such as inert gases including helium, argon, and
nitrogen. These quench gasses are somrtimes used after austenitizing in a vaccum.
The ability of a quenchto harden steel depends on the cooling characteristics of the quenching
medium valadity and quantity. Quenching effectiveness is dependent on the steel chemical
composition , type of quench or the quenchuse conditions. The design of the quenching systemand the thoroughness with which the system is maintained also contribute to the success of the
process.
The reson of the quenching system process is to cool steel from the austenitizingtemperature
quickly enough to form the desire microstructural phases, sometimes bainite but mero often
martensite. The basic quench function is to control the rate of heat transfer from the surface of
the part being quenched.
Quenching process
The rate of heat extraction by a quenching medium and the way it is used substantially affectsquench performance. Variations in quenching partices have resulted in the assignment of specific
names ti some quenching techniques-
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Direct quenching Time quenching Selective quenching Spray quenching Fog quenching Interrupted quenching
Result:-
The study of hardening of steel and effect of quenching medium on hardness has been done.