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Decarb Is.6396.2000 - 0 PDF
Decarb Is.6396.2000 - 0 PDF
Indian Standard
METHODS OF MEASURING DECARBUNZED
DEPTH OF STEEL
(Second Revision )
ICS 77.080
C) BIS 2000
Price Group 2
/;/j.:t[.s/ 2000
Metallography and Heat Treatment Sectional Committee, MTD 22
FOREWORD
This Indian Standard (Second Revision) was adopted by the Bureau of Indian Standards, after the draft finalized
by the Metallography and Heat Treatment Sectional Committee had been approved by the Metallurgical Division
coLlncil,
This standard was first published in 1971 and was revised in 1983. On the basis of experience gained and recent
cievelopments, the committee decided to revise this standard. In the present revision the following modifications
have been made :
c) ASTM and JIS standards have also been considered while considering this revision.
d) A new clause has been added giving details of various IS standards to be referred to in utilizing this
standard.
This standard outlines the methods for measuring and designating decarburized depth of steel.
In the preparation of this standard, assistance has been derived from the following standards:
GOST 1763-42 Method for microscopic determination of decarburized depth in semi-finished and
finished steel products committee of the Russian Federation for Standardization,
Metrology and Certification.
ASTM-E 1077-85 The Society of Automotive Engineers, ‘U.S.A and The American Society of Testing
Mate~ial.
For the purpose of deciding whether a particular requirement of this standard is complied with the final value
observed or calculated, expressing the result of test or analysis, shall be rounded off in accordance with
IS 2: 1960 ‘Rules for rounding off numerical values (revised)’. The number of significant places retained in
the roLmding off value should be the same as that of specified value in this standa:d.
IS 6396:2000
Indian Standard
METHODS OF MEASURING DECARBURIZED
DEPTH OF STEEL
(Second evision )
1 SCOPE homogeneous microstructure.
This standard specifies the following methods of The chemical analysis method is limited to simple
measuring decarburized depth of steel and also lays shapes and is generally used only for research
down the code for designating decarburized depth: investigations.
IS No. Title
228:1959 Methods of chemical analysis of
steels
1501 Method for Vickers hardness test for
metallic materials
5072: 988 Method for Rockwell superficial
6885: 973
hardness test (N&T scales) for steel
Method for knoop hardness testing
L COMPLETE--+PARTIAL
DECARBURIZATION 4
of metals FIG. 1 PARTIAL AND COMPLETE DECARBURIZATION
4.2 Depth of Complete Decarburization
3 SELECTION OF METHOD
The depth below the SLUlace of steel to the zone where
These methods are intended to measure decarburized phases other than ferrite begin to appear. The complete
depth of steel due to heating at elevated temperatures decarburized layer is the layer where only ferrite is
during hot working or by detecting changes in the present.
microstructure, hardness or carbon content at the
surface. The decarburized depth is taken as the depth 4.3 Zone of Partial Decarburization
where a uniform microstructure, hardness or carbon
Itis characterized by partial reduction of carbon
content of the base material is observed.
concentration in the surface layer. In the presence of
3.1 The method to be used is dependent on accuracy a completely decarburized zone, the zone of partial
desired, the degree of decarburization, microstructure decarburization is a transition zone in which the ferrite
and base carbon content of the steel. structure blends into the base structure of the metal.
The microscopic method is sufficiently accurate for — 4.3.1 In the absence of a zone of complete decarbu-
as hc:-rolled, as forged, as annealed and as normalized rization, the zone of partial decarburization shall be
sample’ 5ut not for small amount of decarburization measured from the edge of a micro section to the base
in steels having high carbon (above 0.70 percent), high structure of the metal, whereas in the presence of a
alloy content or high hardness. completely decarburized zone, it shall be measured
Microhardness method is suitable for accurate mea- from the first bands of pearlite or other stmctural
surement of hardened structures with relatively constituent to the base structure of the metal.
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iS 6396:2000
4.4 Total Depth of Decarburization epoxy materials generally give the best edge retention
of the commonly available plastics. An additional
The perpendicular distance from the surface of steel
method of protection is to electroplate a metallic
to the part where the carbon content of the base metal
coating of 0.025 to 0.075 mm on the specimen before
is found. Total depth of decarburization shall be equal
mounting.
to the depth o f complete decarburization pius the depth
of parlia! decarburization, 6.2.1 Polishing must be done in accordance with good
metallographic practice to produce a true represen-
4.5 Decarburized Depth of Specified Residual tation of the surface microstructure.
Carbon Percentage
6.2.2 Etching in 3 percent nital (cone. HNO~ in
The depth from the surface of the steel to the part alcohol) is usually suitable for showing changes in
having the specified residual carbon percentage. microstructure caused by decarburization. Special
etcha’nts may be used, if required, subject to an
4.6 Decarburized Depth of Specified Hardness
agreement between the manufacturer and the
The depth from the surface of the steel to the part purchaser.
where the specified hardness is obtained.
6.3 Measurement
5 SA,MPLING
Generally a magnification of 100 x is used. The
The samples shall be taken at locations that are magnification should be high enough to resolve the
representative of the bulk specimen. The number of structure and to achieve the desired accuracy. If the
test pieces to be used for testing and their selection microscope is of a type with a ground glass screen,
shall be as agreed to between the manufacturer and the extent of decarburization may be measured directly
the purchaser. with a scale. If an eye-piece is used for measurement,
it should have a cross hair or a scale.
6 MICROSCOPIC METHOD
6.3.1 For each sample, several measurements (five at
This method is based on evaluation of the variation in
the maximum) shall be carried out in the deepest
microstructure at the surface due to change in carbon
uniformly decarburized zone. The average of these
content. rneasurernents defines the maximum depths of total
decarburization (see 4.4). Points of extreme depth of
6.1 Specimen
decarburization shall be excluded except if agreed to
The somple to be examined shall be cut at right angles by the Contracting Parties concerned.
to the longih~dina] axis of the product so that mea-
smements are made on a transverse plane. The depth 7 MICROHARDNESS METHOD
of dccarburization shall be determined on semi-
It is suitable for measuring decarburization depth in
finished and finished products in the condition ‘as heat-treated samples. lt is not suitable if two
supp!iwi’. If the products to be evaluated have been
constituents of significantly different hardness are
subjected to hardening or cold-working, they may, present. It is based on the variation in microhardness
bcfol-e examination, be normalized or annealed in such with respect to “the depth below the surface due to
a way ihat they are protected against additional decar- depletion in carbon.
5urization or carburization. For sections up to 25 mm
diameter, the entire cross-section is polished and 7.1 Cross Section Microhardness Traverse
examined. For iar.ger sections, one or more samples
7. LI Specimen
shall be prepared to assess variation in surface
decarburization. Comers of straight sided sections The sample to be checked shall be cut at right angle
shou id not be inc Iuded, since they are not considered to the longitudinal axis of the product so that measure-
rqxwscmtative. ments are made on transverse plane. If cross-section
is too large, a portion of suitable size including surface
6.2 Preparation to be checked should be cut for examination.
.%mp!e polishing shall be done in such a way that 7.L2 Preparation
edge rounding is avoided. Samples, which are small
or of an inconvenient shape, should be mounted in a h case of hardened and tempered material, no further
~lan~p or in a p]astic mount. Compression mounting treatment is necessary. In case of non-hardened
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IS 6396:2000
materials, samples may be hardened by quenching at which no increase in hardness is found. After the
after heating under conditions which minimize hardness traverse, the hardness values need to be
further change in carbon distribution. The soaking plotted on graph paper. The decarburised depth can
period should be minimized to avoid excessive carbon then be determined accurately from the hardness
diffusion. profile.
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IS 6396:2000
BIS is a statutory institution established under the Bureau of Indian Standards Act, 1986 to promote
harmonious development of the activities of standardization, marking and quality certification of goods
and attending to connected matters in the country.
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without the prior permission in writing of BIS. This does not preclude the free use, in the course of
implementing the standard, of necessary details, such as symbols and sizes, type or grade designations.
Enquiries relating to copyright be addressed to the Director (Publications), BIS.
Amendments are issued to standards as the need arises on the basis of comments. Standards are also reviewed
periodically; a standard along with amendments is reaffirmed when such review indicates that no changes are
needed; if the review indicates that changes are needed, it is taken up for revision. Users of Indian Standards
should ascertain that they are in possession of the latest amendments or edition by referring to the latest issue of
‘BIS Catalogue’ and ‘Standards: Monthly Additions’.
This Indian Standard has been developed from Doc : No. MTD 22 (3825).
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