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Steel
is basically iron alloyed to carbon with certain additional elements
to give the required properties to the finished melt. Listed below is
a summary of the effects of alloying various elements in steel. |
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Niobium
(Colombium) (Nb) |
Niobium
is added to steel in order to stabilize carbon, and as such, performs
in the same way as described for titanium. Niobium also has the effect
of strengthening steels and alloys for high temperature service. | |
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Nitrogen
(N) |
Nitrogen
has the effect of increasing the austenitic stability of stainless steels
and is, as in the case of nickel, an austenitic forming element. Yield
strength is greatly improved when nitrogen is added to stainless steels. | |
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Silicon
(Si) |
Silicon
is used as a deoxidizing (killing) agent in the melting of steel, and
as a result, most steels contain a small percentage of silicon. Silicon
contributes to hardening of the ferritic phase in steels and for this
reason silicon killed steels are somewhat harder and stiffer than aluminum
killed steels. | |
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Cobalt
(Cu) |
Cobalt
becomes highly radioactive when exposed to the intense radiation of
nuclear reactors, and as a result, any stainless steel that is in nuclear
service will have a cobalt restriction, usually approximately 0.2% maximum.
This problem is emphasized because there is normally a residual cobalt
content in the nickel used in producing these steels. | |
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Copper
(Cu) |
Copper
is normally present in stainless steel as a residual element. However,
it is added to a few alloys to produce precipitation hardening properties
or to enhance corrosion resistance particularly in sea water environments. | |
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Sulphur
(S) |
When
added in small amounts sulphur improves machinability but does cause
hot shortness. Hot shortness is reduced by the addition of manganese
sulphide. Manganese sulphide has a higher melting point than iron sulphide,
which would form if manganese were not present. The weak spots at the
grain boudaries are greatly reduced during hot working. | |
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Selenium
(Se) |
Selenium is added to improve machinability. | |
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Carbon
(C) |
The
basic metal, iron, is alloyed with carbon to make steel and has the
effect of increasing the hardness and strength of iron. Pure iron cannot
be hardened or strengthened by heat treatment but the addition of carbon
enables a wide range of hardness and strength. | |
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Manganese
(Mn) |
Manganese
is added to steel to improve hot working properties and increase strength,
toughness and hardenability. Manganese, like nickel, is an austenite
forming element and has been used as a substitute for nickel in the
AISI 200 Series of Austenitic Stainless Steels e.g. AISI 202 as a substitute
for AISI 304. | |
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Chromium
(Cr) |
Chromium
is added to steel to increase resistance to oxidation. This resistance
increases as more chromium is added. 'Stainless Steels' have approximately
11% chromium and a very marked degree of general corrosion resistance
when compared to steels with a lower percentage of chromium. When added
to low alloy steels, chromium can increase the response to heat treatment
thus improving hardenability and strength. | |
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Nickel
(Ni) |
Nickel
is added in large amounts, over about 8%, to high chromium stainless
steels to form the most important class of corrosion and heat resisting
steels. These are the austenitic stainless steels, typified by 18-8,
where the tendency of nickel to form Austenite is responsible for great
toughness and high strength at both high and low temperatures. Nickel
also improves resistance to oxidation and corrosion. It increases toughness
at low temperatures when added in smaller amounts to alloy steels. | |
|
Molybdenum
(Mo) |
Molybdenum
when added to chromium-nickel austenitic steels, improves resistance
to pitting corrosion by chlorides and sulphur chemicals. When added
to low alloy steels, Molybdenum improves high temperature strength and
hot hardness. When added to chromium steels, it greatly diminishes the
tendency of steels to embrittle in service or in heat treatment. | |
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Titanium
(Ti) |
The
main use of titanium as an alloying element in steel is for carbide
stabilization. It combines with carbon to form titanium carbides, which
are quite stable and hard to dissolve in steel. This tends to minimize
the occurrence of inter-granular corrosion as with AISI 321, when adding
approximately .25/.60 % titanium, the carbon combines with titanium
in preference to chromium, preventing a tie-up of corrosion resisting
chromium as inter-granular carbides and the accompanying loss of corrosion
resistance at the grain boundaries. | |
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Phosporous
(P) |
Phosphorus
is usually added with sulphur, to improve machinability. In low alloy
steels, phosphorus, in small amounts, aids strength and corrosion resistance.
Experimental work indicates that phosphorus present in austenitic stainless
steels increases strength. Phosphorus additions are known to increase
the tendency to cracking during welding. |
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Corrosion
can be defined as the attack of a metallic material by its environment.
Stainless steels all possess a high resistance to corrosion. This resistance
is conferred by the naturally occuring chromium-rich oxide film which
is always present on the surface of stainless steel. Although less than
130 angstrom thick (1 anstrom unit =108cm) this invisible film is extremely
protective as it is inert and adheres tightly to the metal. |
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The
oxide film has the unique property of self-repair which is unattainable
in applied films. This means that if the film is removed or damaged
or a new metal surface is created by cutting then in the atmosphere
or other source of oxygen the protection will be instantaneously re-established. |
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The
more highly alloyed grades of stainless steel possess the best corrosion
resistance and are able to withstand more aggressive environments. Selection
of the correct grade of stainless steel is the key to the avoidance
of corrosion problems. |
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and Company Incorporated
326/334 Mile Long Building, Amorsolo St., Makati City, Philippines
Telephone: 892-6535, 892-6536, 817-4168; Telefax: 817-1005
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Corrosion
Resistance |
Corrosion
takes many different forms. Its initiation and subsequent rate of progress
is affected in varying degrees by numerous material and environmental
factors. A comprehensive assessment of the exact corrosion resistance
of a material is therefore difficult. However, corrosion tables covering
a vast range of stainless steels and environments are available. | |
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Design
Criteria |
To
achieve optimum corrosion performance care must be taken at the design
stage. In particular design should employ smooth contours and radiused
corners whilst avoiding sharp edges and crevices. Design should also
promote material flow and mixing to avoid localized concentrations and/or
stagnant conditions. Other considerations are ease of cleaning and maintenance
as well as avoidance of dissimilar metal contact. | |
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Acid
Corrosion |
Occurs
due to aggressive attack by acids which may be accelerated by the presence
of other chemicals. A large number of acid environments are resisted
by stainless steels whose resistance to oxidising solutions is particularly
good provided the correct grade is used. | |
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Atmospheric
Corrosion |
Occurs
due to the attack from oxygen, water and the pollutants therein such
as chlorides, sulphur compounds and solids. The problem is particularly
prevalent in coastal and industrial areas which necessitates the use
of type 316 for outdoor applications in such environments. | |
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Bacterial
Corrosion |
Occurs
due to the presence and activity of certain types of bacteria and tends
to be localized, for example in crevices. It is overcome by good design,
continuous flow and regular cleaning. | |
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Crevice
Corrosion |
Is
a form of galvanic corrosion which occurs in crevices such as joints,
cavities, holes, corners, and gaps between components. Good design should
eliminate such crevices. | |
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Fretting
Corrosion |
Which could also be called corrosion-abrasion is caused by continuous removal of corrosion product due to surfaces rubbing together which leads to progressive wasting of material. Stainless steels do not suffer from this form of attack. | |
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Galvanic
Corrosion |
Covers
situations where attack is caused by a potential difference. This potential
difference can be set up in a number of ways including contact between
dissimilar metals in an aqueous or conducting solution, differential
aeration (variation in oxygen concentration) and local variations in
concentration of the solution. Correct material selection and good design
eliminate this activity. | |
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General
Corrosion |
Is
the uniform overall attack of a component across its whole surface.
It is avoided by correct grade selection. | |
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Inter-Granular
Corrosion |
Is
the uniform overall attack of a component across its whole surface.
It is avoided by correct grade selection. | |
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Oxidation |
Oxidation
is the combination of a metal with oxygen to form the metal oxide which
occurs in dry conditions. When this process is ongoing the whole of
the metal may be converted. Stainless steels are oxidation resistant,
even at elevated temperatures. Special grades, such as type 310, are
operated at temperatures of up to 1100 degrees centigrade. The surface
of all stainless steels is oxidized to form a chromium rich oxide film
which is inert, self-repairing and forms a proctective barrier keeping
oxygen away from the metal surface. | |
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Pitting
Corrosion |
Is
the highly localized attack seen as small spots across a surface occuring
mainly at sites of metallurgical heterogeneity. It is particulary prevalent
in chloride environments especially if oxygen is in plentiful supply.
Higher chromium, nickel and molybdenum contents improve pitting resistance
with type 316 being used extensively in such situations. | |
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Stress
Corrosion |
Cracking
can occur in austenitic stainless steels when they are operated under
tensional stress in chloride environments at temperatures in excess
of about 60 degrees centigrade. The stress could arise through in-service
loading, pressurization of pipework and vessels or as residual stress
from cold working. Ferritic stainless steels are immune to this form
attack. | |
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Waterline
Corrosion |
Is a form of Galvanic corrosion taking place at the liquid surface. | |
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Weld
Decay Corrosion |
Is a form of inter-granular corrosion occuring in the heat-affected zone of the parent metal parallel to the weld. Susceptibility to this attack is assessed using one of these standard tests: | |
| 1.)Test as given in BS 1449/BS 1501 using boiling copper sulphate/sulphuric acid. | ||
| 2.)Test as given in ASTM A262-75 Practice C using boiling nitric acid. | ||
| Low carbon grades perform better in the more severe (latter) test. |