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Transcript of Rubber technology A
SUMMRUBBER
TECHNOLOGYWritten & Edited by Subrata Das (M.Tech,Polymer)
In this paper I have tried a very brief knowledge sharing about the Rubber
Technology. One thing we have to remember that the Rubber Technology is
vast subject.
SUMMARY ON RUBBER
TECHNOLOGYWritten & Edited by Subrata Das (M.Tech,Polymer)
Subrata Das
4/10/2014
In this paper I have tried a very brief knowledge sharing about the Rubber
Technology. One thing we have to remember that the Rubber Technology is
RY ON
TECHNOLOGY Written & Edited by Subrata Das (M.Tech,Polymer)
In this paper I have tried a very brief knowledge sharing about the Rubber
Technology. One thing we have to remember that the Rubber Technology is a very
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CONTENT
Introduction ................................................................................................................................... 2
Rubber materials ........................................................................................................................... 3Ethylene Propylene Rubber (EPDM/EPM) .................................................................................... 3Nitrile rubber (NBR) .................................................................................................................... 3Natural Rubber (NR) ................................................................................................................... 3Styrene - Butadien Rubber (SBR) ................................................................................................ 3Chloroprene rubber (CR)............................................................................................................. 3Silicone (VMQ/MVQ/HTV) ........................................................................................................... 3Acrylic rubber (ACM)................................................................................................................... 4Hydrogenated Nitrile Butadiene Rubber (HNBR) ........................................................................... 4Fluoro rubber (FKM) ................................................................................................................... 4Rubber properties .......................................................................................................................... 6Specific gravity ........................................................................................................................... 6Hardness ................................................................................................................................... 6Tensile strength, elongation......................................................................................................... 7Compression set......................................................................................................................... 7Resistance to heat aging............................................................................................................. 7Rubber ingredients......................................................................................................................... 9Fillers ......................................................................................................................................... 9Plasticizers................................................................................................................................. 9Vulcanization chemicals .............................................................................................................. 9Accelerators ............................................................................................................................... 9Activators ................................................................................................................................... 9Anti degrading agents ................................................................................................................. 9Process aids............................................................................................................................... 9Pigments.................................................................................................................................... 9Rubber compounding................................................................................................................... 10Open mill.................................................................................................................................. 10Internal mixer ........................................................................................................................... 10Compound control .................................................................................................................... 11Rubber moulding ......................................................................................................................... 12Compression moulding.............................................................................................................. 12Injection moulding..................................................................................................................... 13Transfer moulding..................................................................................................................... 14Secondary finishing................................................................................................................... 17Rubber extrusion ......................................................................................................................... 18Dimensional tolerances .../Rubber cable Technology(20/36)/Properties of different Rubbers/Elastomers(28/36).............................................................................................................
19
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INTRODUCTION
Rubbers are described as materials which show “elastic” properties. Such materials are
generally long chain molecules known as “polymers” and the combination of elastic and
polymers has led to the alternative name of “elastomers”. Rubbers and elastomers will be
considered to be synonymous in this work.
Products made from rubber have a flexible and stable 3–dimensional chemical structure and
are able to withstand under force large deformations. For example the material can be
stretched repeatedly to at least twice its original length and, upon immediate release of the
stress, will return with force to approximately its original length.
Under load the product should not show creep or relaxation. Besides these properties the
modulus of rubber is from hundred to ten thousand times lower compared to other solid
materials like steel, plastics and ceramics. This combination of unique properties gives rubber
its specific applications like seals, shock absorbers, cables and tyres.
Rubber is used as a name for 3 categories:
Raw or base polymers These determine the main characteristics of the final product.
Semi-manufactured The addition to raw rubber of various chemicals, to impart desirable product properties, is termed compounding. This semi-finished material is getting its rubber properties after vulcanization. Final product After moulding the rubber compounds gets its elastic properties after a vulcanisation process.
Modern rubber materials consist of approximately 60 percent of synthetic polymers. The
other part consists of vulcanisation agents, softeners, accelerators, anti aging agents and other
chemicals. These additions are necessary to achieve the desired properties of the final
product.
Bonded flexible chains
Polymers have a backbone of hydrocarbons. The hydrogen atom is often replaced by other
atoms or molecules (like CH3, Cl or F) and thus create another type of elastomer. These
chains are chemically bonded together by sulphur, peroxides or bisphenol. An exception is
silicone. Silicone contain very flexible siloxane backbones (Si-O) and can be cured with
peroxide or platinum-catalyst curing.
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RUBBER MATERIALS
The most common elastomers are:
Ethylene Propylene Rubber (EPDM/EPM)
EPM is a copolymer of ethylene and propylene. This type can only be crosslinked with peroxides. If
during the copolymerization of ethylene and propylene, a third monomer, a diene, is added the
resulting rubber will have unsaturation and it can then be vulcanized with sulphur. These rubbers are
the so-called EPDM’s.
The main properties of EPDM are its outstanding heat, ozone and weather resistance. The resistance
to polar substances and steam are also good. It has excellent electrical insulating properties. The
EPDM copolymer can be filled with more than 200 percent of its own weight with non re-inforcing
fillers, resulting in reduction of costprice but also in physical properties. For these reasons this rubber
is widely applied in many applications.
Nitrile rubber (NBR)
NBR is a family of unsaturated copolymers of acrylonnitrile (CAN) and butadiene monomers.
Although its physical and chemical properties vary depending on the polymer’s composition of nitrile
(the more nitrile within the polymer, the higher the resistance to oils but the lower the flexibility of the
material), this form of synthetic rubber is generally resistant to oil, fuel, and other chemicals. It is used
in the automotive industry to make fuel and oil handling hoses, seals, and grommets.
NBR’s ability to withstand a range of temperatures from -25 °C to +108 °C makes it an ideal material
for automotive applications. Nitrile rubber is more resistant than natural rubber to oils and acids, but
has less strength and flexibility. Nitrile rubber is generally resistant to aliphatic hydrocarbons. Nitrile,
like natural rubber, can be attacked by ozone, aromatic hydrocarbons, ketones, esters and aldehydes.
Natural Rubber (NR)
Natural rubber has a very high elasticity, high tensile strength and a very good abrasion resistance.
The material is obtained by coagulation of latex derived from the rubber tree. The rubber is not
resistant to aging and oil. For these reasons NR is rarely used as a seal for technical applications, but
is mixed with other elastomere compounds like EPDM to improve rubber properties.
Styrene - Butadien Rubber (SBR)
SBR is a synthetic rubber copolymer consisting of styrene and butadiene. It has good abrasion
resistance and good aging stability when protected by additives, and is widely used in car tyres, where
it is blended with natural rubber.
Chloroprene rubber (CR)
Commonly known under the trade name Neoprene® of Dupont. CR is not characterised by one
outstanding property, but its balance of properties is unique among the synthetic elastomers. It has
good mechanical strength, high ozone and weather resistance, good aging resistance, low
flammability, good resistance toward chemicals and moderate oil and fuel resistance.
Silicone (VMQ/MVQ/HTV)
Silicones differ from other polymers in that their backbones consist of Si-O-Si units unlike many
other polymers that contain carbon backbones.
Silicone rubber offers good resistance to extreme temperatures, being able to operate
normally from -70 °C to +230 °C. At the extreme temperatures, the tensile strength,
elongation, tear strength and compression set can be far superior to conventional rubbers
although still low relative to other
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materials. Organic rubber has a carbon to carbon backbone which can leave them susceptible to ozone, UV, heat
and other ageing factors that silicone rubber can withstand well. This makes it one of the elastomers of choice in
many extreme environments.
Compared to organic rubbers, however, the tensile strength of standard silicone rubber is lower. For this reason,
care is needed in designing products to withstand low imposed loads. Nowadays also silicone compounds with
improved tensile strength are available.
Acrylic rubber (ACM)
Acrylic rubber, known by the chemical name alkyl acrylate copolymer (ACM), is a type of rubber that has
outstanding resistance to hot oil and oxidation. It has a continuous working temperature of 150 °C and an
intermittent limit of 180 °C. Disadvantages are its low resistance to moisture, acids, and bases. It should not be
used in temperatures below -10 °C. It is commonly used in automotive transmissions and hoses.
Hydrogenated Nitrile Butadiene Rubber (HNBR)
The properties of hydrogenated nitrile rubber depend on the acrylonitrile (ACN) content, and on the degree of
hydrogenation. They can be ‘tailored’ to particular applications, but have the general advantage over standard
nitrile rubber of having higher temperature resistance and higher strength.
HNBR’s also have good high temperature oil and chemical resistance and are resistant to amines. They are
suitable for use in methanol and methanol/hydrocarbon mixtures if the correct ACN level is selected. They have
good resistance to hot water and steam. They can have excellent mechanical properties including strength,
elongation, tear resistance, abrasion resistance and compression set. For the best properties peroxide curing is
used, unless low hysteresis is required. They are reported to be satisfactory up to temperatures around 180 °C in
oil. Fully saturated grades have excellent ozone resistance. They have poor resistance to some oxygenated
solvents and aromatic hydrocarbons.
Fluoro rubber (FKM)
Fluoroelastomers are a class of synthetic rubber which provide extraordinary levels of resistance to chemicals,
oil and heat, while providing useful service life above 204°C. The outstanding heat stability and excellent oil
resistance of these materials are due to the high ratio of fluorine to hydrogen, the strength of the carbon-fluorine
bond, and the absence of unsaturation.
The original fluoroelastomer was a copolymer of hexafluoropropylene (HFP) and vinylidene fluoride (VF2). It
was developed by the DuPont Company in 1957 in response to high performance sealing needs in the aerospace
industry. To provide even greater thermal stability and solvent resistance, tetrafluoroethylene (TFE) containing
fluoroelastomer terpolymers were introduced in 1959 and in the mid to late 1960’s lower viscosity versions of
FKMs were introduced A breakthrough in cross linking occurred with the introduction of the bisphenol cure
system in the 1970’s. This bisphenol cure system offered much improved heat and compression set resistance
with better scorch safety and faster cure speed. In the late 70’s and early 80’s fluoroelastomers with improved
low temperature flexibility were introduced by using perfluoromethylvinyl ether (PMVE) in place of HFP.
Fluoroelastomers are a family of fluoropolymer rubbers, not a single entity. Fluoroelastomers can be classified
by their fluorine content, 66%, 68% and 70% respectively. Fluoroelastomers having higher fluorine content
have increasing fluids resistance derived from increasing fluorine levels. Peroxide cured fluoroelastomers have
inherently better water, steam, and acid resistance.
Fluoroelastomers are used in a wide variety of high-performance applications. FKM provides premium, long-
term reliability even in harsh environments. A partial listing of current end use applications (industries like
aerospace and automotive) include: O-ring seals in fuels, lubricants and hydraulic systems, shaft seals, valve
stem seals, fuel injector O-rings, diaphragms, lathe cut gaskets and cut gaskets.
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Common name CHLORINATED POLYETHYLENE
Chemical name
Abbreviation CPE
Good chemical resistance to hydrocarbon fluids and elevated temperatures. Used for hose linings. Poor mechanical strength. Mechanical properties may deteriorate above 100C.
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Common name CHLOROSULPHONATED POLYETHYLENE
Chemical name
Abbreviation CSM
Trade names Hypalon®
This is a material with Neoprene polychloroprene 'plus' qualities. It is suitable for continuous use up to about 130C and intermittent use up to some 30C above this. It has excellent resistance to oxygen, ozone and most chemicals, including water, but has poor fuel resistance. It has low gas permeability. It has poor compression set resistance which limits its usefulness in dynamic sealing applications.
The following table provides a summary of the various elastomer groups and their names
according the ISO 1629 standard.
Designation Trade name Abbreviation
ISO 1629 Acrylonitrile Butadiene rubber JSR-230S NBR NIPOL Hydrogenated Acrylonitrile Butadiene rubber Therban® HNBR Zetpol® Butyl rubber Esso Butyl® IIR Chloroprene rubber Neoprene® CR ChloroSulphonatedPolyethylene Hypalon CSP Ethylene Propylene Diene Rubber Royalene EPDM Keltan® Fluorocarbon rubber Viton® FKM Fluorel® Chlorinated Polyethylene Tyrene CPE Silicone rubber Elastosil® MVQ Rhodorsil® Silopren® Fluorosilicone rubber Silastic® FMVQ Perfluoro rubber Kalrez® FFKM Chemraz® Tetrafluorethylene-Propylene Copolymeer Aflas® FEPM Polyester Urethane Adiprene® AU Polyether Urethane Pellethan® EU
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RUBBER PROPERTIES
Elastomers and rubber materials provide a variety of properties. Important specifications for elastomers and
rubber materials include mechanical, thermal, electrical, optical, processing, and physical properties.
Mechanical properties include tear strength (TS), ultimate tensile strength (UTS), tensile modulus or modulus of
elasticity, elongation, and impact toughness as measured with an Izod test and a notched sample.
Thermal properties include maximum use temperature, glass transition temperature, thermal conductivity, and
coefficient of thermal expansion (CTE).
Electrical and optical properties include electrical resistivity, dielectric strength, dielectric constant or relative
permittivity, index of refraction, and light transmission. Processing and physical properties include bulk or
apparent density, water absorption, vi scosity, process temperature, and melt flow index (MFI).
To make it possible to compare the different material characteristics several tests have been standardized. The
material datasheets provide the results of these tests. Below the most important properties are explained in more
detail.
Specific gravity
This property is fully defined by the composition of the material. Any other value will indicate another material
or composition is on hand. The specific gravity is the mass per unit volume and is measured by weighing the
sample in air and in water.
Specific gravity = weight in air / (weight in air – weight in water)
Standards: ISO 2871, ASTM D 1817
Hardness
Hardness represents the elasticity of the material. The lower the hardness the more elastic the material is. Two
scales are normally used: Shore-A and micro-IRHD. They are roughly the same. The instruments used for the
measurement are:
Durometer: a pointed conical indentor when pressed against a sample, is pushed back into the case of the tester
against a spring and this motion is translated into movement of the pointer on the dial. The harder the sample the
farther it will push back the indentor point and the higher will be the numerical reading on the scale. The unit is
Shore-A.
IRHD tester: a dead-load is applied to the indentor for a specific time and the hardness is obtained from the
depth of the indentation.
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Standards: ISO 48, ISO 1400, ISO 1818, ASTM D 2240, ASTM D 1415
Tensile strength, elongation
Tensile strength is the maximum tensile stress reached in stretching a test piece, usually a flat
dumb- bell shape, to its breaking point. By convention, the force required is expressed as
force per unit area of the original cross section of the test length.
Elongation, or strain, is the extension between bench marks produced by a tensile force
applied to the test piece and is expressed as a percentage of the original distance between the
marks. Elongation at break, or ultimate elongation, is the elongation at the moment of
rupture.
Standards: ISO 37, ASTM D 412
Compression set
Rubbers deform under load and rarely return completely to their original dimensions when
the load is removed. The difference between the original and final dimensions is known as
compression set. Small cylindrical disks of 13 mm diameter and a thickness of 6 mm or 29
mm diameter and a thickness of 12.5 mm are being used to perform the tests.
The disks are compressed in such a way that the compression is 25 percent of the original
height. This at a known temperature, often at 23°C (or between 70 and 250°C) with a
duration of 24 or 72 hours.
At the end of the specified time, the test pieces are removed from the test jig and allowed to
recover at 23°C for 30 minutes before the thickness is re-measured. The compression set is
the difference between the original thickness of the test piece and that after recovery,
expressed as a percentage of the initially applied compression.
As formula:
Compression set = ( Original thickness – Thickness of the piece after recovery ) / ( Original
thickness
– Height of the compression )
Standards: ISO 815, ASTM D 395
Resistance to heat aging
The properties of an elastomer will generally change after prolonged exposure to high
temperatures. Tests for heat aging are carried out for two reasons. Firstly, there are tests to
establish the changes in physical properties at elevated service temperatures. Secondly, there
are accelerated tests at high
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temperatures which attempt to predict the long-term life at lower temperatures. Tests are carried out in
an air oven or an oxygen pressure chamber.
Standards: ISO 188, ASTM D 573
Resistance to weathering
Deterioration in physical properties can occur when elastomers are exposed to the weather. This
deterioration can be observed as cracking, peeling, chalking, colour changes and other surface defects.
By far the most important cause of deterioration by weathering is the presence of ozone. Less than
one pphm of ozone in the atmosphere can severely attack non-resistant rubbers if they are in a slightly
strained condition. The result are cracks sheer on the direction of the strain. Sunlight (UV), oxygen,
moisture and temperature also affect elastomers.
Standards: 1431/1, ASTM D 1149
Resistance to low temperatures
All elastomers undergo several kinds of change when they are exposed to low temperatures. Some of
the changes occur immediately, others after prolonged exposure. All are reversible; the elastomer
regaining its original properties when it is returned to room temperature. At low temperatures the
material will become brittle and shatter on sudden bending or impact.
The temperature at which this occurs, when determined under certain prescribed testing conditions, is
called the brittle point. Another test, to measure the modulus of the material, is the material retraction
test. Generally known as the TR test.
Standards: ISO R 812, ISO 2921, ASTM D 2137, ADTM D 1053, ASTM D 1329
Abrasion resistance
A test piece is pressed against a rotating drum covered with an abrasive cloth. The loss in weight
(volume) is measured after a certain number of revolutions and gives an indication of the abrasion
resistance.
Standards: ISO 4649, ASTM D 394
Resistance to liquids
The action of liquids on elastomers may result in the absorption of liquid by the elastomer, extraction
of soluble constituents from the elastomer or chemical reaction with the elastomer. Absorption is
usually greater than extraction and there is a net increase in volume, generally known as swelling. For
some products a decrease in volume or dimensions could be more serious than swelling and if there is
a significant chemical reaction a low swelling may hide a large deterioration in physical properties.
Consequently, although degree of swelling provides a good general indication of resistance it is also
important to measure the change in other properties. In general the following guide lines can be used:
0-5% swell; recommended, no or minor effect
5-10% swell; seal can be used in most cases, less to moderate effect.
10-20% swell; Seals only in static applications to be used, moderate to severe effect > 20% swell; not
recommended
Standards: ISO 1817, ASTM D 1817
Of course, many more properties can be tested. Depending on the application the most appropriate
tests can be selected and carried out to give the best results to predict the life time of a product.
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RUBBER INGREDIENTSRUBBER INGREDIENTSRUBBER INGREDIENTSRUBBER INGREDIENTS
A rubber compound is obtained by mixing a base polymer or crude mixture with a series of additives.
The choice of the base polymer and the additives is closely linked to the type of properties to be achieved.
The resulting product is a non vulcanized compound. The quantity of additives used varies for 20 to 130
percent as a percentage on the weight. The most common additives are:
Fillers
There are two types of fillers, reinforcing and non reinforcing fillers. Reinforcing fillers are also of two
types, black and non black. Carbon black is commonly used as black reinforcing filler. Silica is the
perfect example of nonblack reinforcing filler. Calcium carbonate, china clay are the example of a non
reinforcing filler. These are called as cost reducing filler.
Plasticizers
Besides fillers, plasticizers play the biggest quantitative role in building a rubber compound. The reasons
for the use of plasticizers are: improvement of flow of the rubber during processing, improved filler
dispersion, influence on the physical properties of the vulcanizate at low temperatures. Mineral oils and
paraffins are widely used as a plasticizer.
Vulcanization chemicals
Vulcanization is the conversion of rubber molecules into a network by formation of crosslinks.
Vulcanizing agents are necessary for the crosslink formation. These vulcanizing agents are mostly
sulphur or peroxide and sometimes other special vulcanizing agents or high energy radiation. Since
vulcanization is the process of converting the gum-elastic raw material into the rubber-elastic end
product, the ultimate properties like hardness and elasticity depend on the course of the vulcanization.
Accelerators
Accelerating agents increase the rate of the cross linking reaction and lower the sulphur content
necessary to achieve optimum vulcanizate properties.
Activators
Like zinc-oxide and stearic acid. They activate the vulcanisation process and help the accelerators to
achieve their full potential.
Anti degrading agents
These agents increase the resistance to attacks of ozone, UV light and oxygen.
Process aids
Chemicals that improve the processability.
Pigments
Organic and inorganic pigments are used to colour rubber compounds. The colour pigments are also
considered inactive fillers. Only silica’s have a reinforcing effect. Silicone can be coloured easily without
loss of properties.
RUBBER COMPOUNDING 9/36
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Compounding is the operation of bringing together all the ingredients required to mix a batch of rubber
compound. Each component has a different mix of ingredients according to the
that component. Rubber compounding is generally carried out on open mills or internal mixers.
Open mill
An open mill consists of twin counter
working to the rubber. The rolls can be heated or cooled as necessary. The rubber is placed on the rolls
and mixing is achieved by the shearing action induced at the “nip” between the rolls. Additives are added
in carefully weighed quantities during the mixing process. After the m
compound is removed from the mill in the form of sheet.
Internal mixer
Internal mixers are often equipped with two counter
rubber charge along with the additives. The
ingredients in the desired order. The shearing action generates considerable heat, so both rotors and
housing are water-cooled to maintain a temperature low enough to assure that vulcanization d
begin.
Compounding is the operation of bringing together all the ingredients required to mix a batch of rubber
compound. Each component has a different mix of ingredients according to the properties required for
that component. Rubber compounding is generally carried out on open mills or internal mixers.
An open mill consists of twin counter-rotating rolls, one serrated, that provide additional mechanical
e rolls can be heated or cooled as necessary. The rubber is placed on the rolls
and mixing is achieved by the shearing action induced at the “nip” between the rolls. Additives are added
in carefully weighed quantities during the mixing process. After the mixing operation is complete, the
compound is removed from the mill in the form of sheet.
Internal mixers are often equipped with two counter-rotating rotors in a large housing that shear the
rubber charge along with the additives. The mixing can be done in three or four stages to incorporate the
ingredients in the desired order. The shearing action generates considerable heat, so both rotors and
cooled to maintain a temperature low enough to assure that vulcanization d
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Compounding is the operation of bringing together all the ingredients required to mix a batch of rubber
properties required for
that component. Rubber compounding is generally carried out on open mills or internal mixers.
rotating rolls, one serrated, that provide additional mechanical
e rolls can be heated or cooled as necessary. The rubber is placed on the rolls
and mixing is achieved by the shearing action induced at the “nip” between the rolls. Additives are added
ixing operation is complete, the
rotating rotors in a large housing that shear the
mixing can be done in three or four stages to incorporate the
ingredients in the desired order. The shearing action generates considerable heat, so both rotors and
cooled to maintain a temperature low enough to assure that vulcanization does not
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Compound control
The properties of the final product are mainly determined by the properties of the compound.
Before starting the production of the final products the compound is tested to guarantee the
correct properties. This is a common applied and standard procedure in rubber compounding.
A rheometer test is carried out on every single batch of compound.
The rheometer describes precisely and quickly curing and processing characteristics of
vulcanizable rubber compounds. It works on a very simple principle. A test piece of rubber
compound is contained in a sealed test cavity under positive pressure and maintained at a
specified elevated temperature. A rotor is embedded in the test piece and is oscillated through a
small specified rotary amplitude. This action exerts a shear strain on the test piece and the
torque (force) required to oscillate the disc depends upon the stiffness of the rubber compound.
The stiffness of the specimen compound increases when cross links are formed during cure. A
plot of this torque (force) value against time gives a typical graph called rheometer curve.
The cure curve obtained with rheometer is a finger print of compound's vulcanization and
processing character.
Of course hardness and tensile strength are also checked for every batch. When all values are
within allowed parameters the compound is released for production.
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RUBBER MOULDING
Moulded rubber parts can be produced by different manufacturing methods. Major
techniques are:
Compression moulding
Compression moulding is a process in which a compound is squeezed into a preheated
mould taking a shape of the mould cavity and performing curing due to heat and
pressure applied to the material. The method uses a split mould mounted in a hydraulic
press
Compression moulding process involves the following steps:
1.A pre-weighed amount of the compound is placed into the lower half of the mould. The
compound may be in form of putty-like masses or pre-formed blanks.
2.The upper half of the mould moves downwards, pressing on the compound and forcing it to fill the mould cavity. The
mould, equipped with a heating system, provides curing (cross-linking) of the compound
3.The mould is opened and the part is removed for necessary secondary operations
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Injection moulding
Injection moulding is a process in which the compound is forced under high pressure
into a mould cavity through an opening (sprue).
The rubber material in form of strips is fed into an injection moulding machine. The
material is then conveyed forward by a feeding screw and forced into a split mould,
filling its cavity through a feeding system with sprue gate and runners.
An injection moulding machine is similar to an extruder. The main difference between
the two machines is in screw operation. In the extruder type the screw rotates
continuously providing output of continuous long product (pipe, rod, sheet).The screw
of the injection moulding machine is called a reciprocating screw since it not only
rotates but also moves forward and backward according to the steps of the moulding
cycle.
It acts as a ram in the filling step when the compound is injected into the mould and
then it retracts backward in the moulding step. The mould is equipped with a heating
system providing controlled heating and vulcanization of the material.
The compound is held in the mould until the vulcanization has completed and then the
mould opens and the part is removed from the mould.
Injection moulding is a highly productive method providing high accuracy and control
of shape of the manufactured parts. The method is profitable in mass production of
large number of identical parts. A principal scheme of an injection moulding machine is
shown here.
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Transfer moulding Transfer moulding is a process in which a pre-weighed amount of a compound is preheated in
a separate chamber (transfer pot) and then forced into a preheated mould through a sprue,
taking a shape of the mould cavity and performing curing due to heat and pressure applied to
the material. The picture below illustrates the transfer moulding process.
The method uses a split mould and a third plate equipped with a plunger mounted in a
hydraulic press. The method combines features of both compression moulding (hydraulic
pressing) and injection moulding (ram-plunger and filling the mould through a sprue).
The transfer moulding process involves the following steps:
1.A pre-weighed amount of a compound is placed into the transfer pot. The compound form
putty-like masses or pre-formed blanks. The compound is heated in the pot where the
material softens.
2.The plunger, mounted on the top plate, moves downwards, pressing on the material and forcing it to fill the mould cavity through
the sprue. The mould, equipped with a heating system, provides curing (cross-linking) of the compound.
3.The mould is opened and the parts are removed for necessary secondary operations
The scrap left on the pot bottom (cull), in the sprue and in the channels is removed. Scrap of
vulcanized rubber is not recyclable.
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The transfer moulding cycle time is shorter than compression moulding
cycle but longer than the injection moulding cycle. The method is capable
to produce more complicated shapes than compression moulding but not as
complicated as injection moulding.
Transfer moulding is suitable for moulding with ceramic or metallic inserts
which are placed in the mould cavity. When the heated compound fills the
mould it forms bonding with the insert surface.
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Secondary finishing
Depending on the requirements and production process, some secondary finishing steps
might be necessary or required:
Aftervulcanisation
Some rubber types require a process of aftervulcanisation (heating) for some hours.
HNBR and FKM rubber is aftervulcanised to give the rubber its optimal mechanical
properties after moulding.
Postcuring
Silicones parts applied in food or medical applications are mostly post cured after
moulding. Post- curing is one of the principal tools to mitigate outgassing. Post-cure is a
process that removes the volatiles from the cross-linked silicone rubber by diffusion and
evaporation and is carried out at a temperature greater than the service temperature
for the part. Post-curing also helps to improve the compression set.
Cryogene finishing
Cryogene deflashing and deburring is a step that is meant to remove excess
imperfections on moulded parts such as fleece or flash lines. The process uses liquid
nitrogen, high speed rotation and media (shot blast) in varying combinations to remove
the flash in a highly precise and expedient manner.
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RUBBER EXTRUSION
In the extrusion process of rubber, the compound including polymers, various types of additives
and fills like curing agents, antioxidants, pigments are fed into the extruder. The extruder
typically consists of a rotating screw inside a cl
of the extruder is to do three things, a) soften, b) mix, c) pressurize the rubber as it is fed
continuously to the die at the extruder exit.
The die is a sort of metal disk that has a machined opening in the desired shape of the
needs to be extruded. The rubber already softened by heating is then forced by the rotating
screw through the die opening into the shape of the profile cut in the die. A typical phenomenon
called die swell takes place as the rubber shape leaves t
section becomes larger than the die cross
material may rise up to several folds over the die.
Subsequently the processes of vulcanization or curing takes place as the l
extrusion process. This aids the rubber extruded profiles to maintain its shape and acquire
necessary physical properties. Typical examples of extruded rubber parts are profiles, hosesstrips and cords and cables.
Generally the extruded cable
(for smaller length). For that
cotton tape over sheath during extrusion
may be swelled or blisters ma
tape rolls are changed when it exhausted, at that time few wrinkles are observed
due to looseness of the tape at that particular portion, it is a mare impression of that
loose tape, nothing else. Aft
surface manually. During removal of the tape, some residual thread from the edge
of the tape remains on the surface. To remove that residual thread
rubbed by emery (sand) paper on the surfa
surface. During rubbing sometime very fine scratch mark comes on the surface, but
magnitude is negligible and for that no physical properties are changed. After
removal of tape, printing is done followed by powder
the cable sheath is extruded and vulcanised online by means of
vulcanizing (CV) process. In this case the surface of the cable shall be smooth finish. 18/36
extrusion process of rubber, the compound including polymers, various types of additives
and fills like curing agents, antioxidants, pigments are fed into the extruder. The extruder
typically consists of a rotating screw inside a closely fitted heated barrel. The
of the extruder is to do three things, a) soften, b) mix, c) pressurize the rubber as it is fed
continuously to the die at the extruder exit.
The die is a sort of metal disk that has a machined opening in the desired shape of the
needs to be extruded. The rubber already softened by heating is then forced by the rotating
screw through the die opening into the shape of the profile cut in the die. A typical phenomenon
called die swell takes place as the rubber shape leaves the die. Because of this the part cross
section becomes larger than the die cross-section. The part cross-section depending on the
material may rise up to several folds over the die.
Subsequently the processes of vulcanization or curing takes place as the last step in the
extrusion process. This aids the rubber extruded profiles to maintain its shape and acquire
necessary physical properties. Typical examples of extruded rubber parts are profiles, hoses
extruded cables are vulcanized in autoclave, called batch process
length). For that somebody have to apply powder and rubberised
e over sheath during extrusion , it acts as a binder tape, otherwise cable
may be swelled or blisters may form during vulcanization. During online taping, the
tape rolls are changed when it exhausted, at that time few wrinkles are observed
tape at that particular portion, it is a mare impression of that
loose tape, nothing else. After curing, the tape has to be removed
surface manually. During removal of the tape, some residual thread from the edge
of the tape remains on the surface. To remove that residual thread the sheath is
emery (sand) paper on the surface, the thread is removed easily from the
surface. During rubbing sometime very fine scratch mark comes on the surface, but
magnitude is negligible and for that no physical properties are changed. After
removal of tape, printing is done followed by powder removing. For longer length
the cable sheath is extruded and vulcanised online by means of continuous
In this case the surface of the cable shall be smooth finish.
extrusion process of rubber, the compound including polymers, various types of additives
and fills like curing agents, antioxidants, pigments are fed into the extruder. The extruder
rel. The primary purpose
of the extruder is to do three things, a) soften, b) mix, c) pressurize the rubber as it is fed
The die is a sort of metal disk that has a machined opening in the desired shape of the part that
needs to be extruded. The rubber already softened by heating is then forced by the rotating
screw through the die opening into the shape of the profile cut in the die. A typical phenomenon
he die. Because of this the part cross-
section depending on the
ast step in the
extrusion process. This aids the rubber extruded profiles to maintain its shape and acquire
necessary physical properties. Typical examples of extruded rubber parts are profiles, hoses,
batch process
have to apply powder and rubberised
, it acts as a binder tape, otherwise cable
y form during vulcanization. During online taping, the
tape rolls are changed when it exhausted, at that time few wrinkles are observed
tape at that particular portion, it is a mare impression of that
has to be removed from the cable
surface manually. During removal of the tape, some residual thread from the edge
the sheath is
ce, the thread is removed easily from the
surface. During rubbing sometime very fine scratch mark comes on the surface, but
magnitude is negligible and for that no physical properties are changed. After
For longer length,
continuous
In this case the surface of the cable shall be smooth finish.
19/36
DIMENSIONAL TOLERANCES
Rubber products are subject to changes in their dimensions after processing and
vulcanisation. This may due to a variety of factors, such as mould shrinkage or relaxation of
die swell. These changes should be determined and allowed for when designing such items as
moulds and dies used in the manufacture of a given product.
All rubbers show some shrinkage when cooled after moulding, and allowance for this is made
in the mould design. The amount of shrinkage is dependent on the rubber compound and the
mix used, but also varies from batch to batch of the same compound. Also moulds are made
in various ways depending on the type of product and accuracy demanded.
In general, the product can be no more accurate than the mould, and the greater the degree of
accuracy demanded, the more expensive become the moulds and their maintenance.
A commonly applied standard for dimensional tolerances for rubber mouldings is described
in ISO 3302-1. In these standard two sets of tolerances, F and C, are given and defined. F
(fixed) dimensions are dimensions which are not affected by deforming influences like flash
thickness or lateral displacement of different mould parts (see l1, l2 and l3).
C (closure) dimensions are dimensions which can be altered by variation in the flash
thickness or lateral displacement of different mould parts (see d1, d2, d3 and h).
The standard established four classes of tolerances for fixed and closure dimensions, varying
from M1 (high precision mouldings) to M4 (non-critical dimensional control). The tolerances
to be applied shall be chosen, by agreement between interested parties from the classes F and
C.
19/36
20/36
RUBBER CABLE TECHNOLOGY
GOVERNING SPECIFICATIONS OF RUBBER CABLES
PURPOSE: TO IDENTIFY CABLE AGAINST SPECN.
S.No. ITEM GOVERNING SPEC.
1. FLEXIBLE TRAILING CABLE IS-9968 Part-1/ PART-II / IEC-60245/ NEMA-WC-8/ MODIFIED
SHDGC/ BS-616
2. HIGH TENSION RUBBER CABLE IS-9968 Part-II / IS-14494
3. FLEXIBLE TRAILING CABLE FOR COAL
MINES
IS-14494
4. FLEXIBLE TRAILING CABLE FOR
QUARRIES & METALLIFEROUS MINES
IS-14494
5. FLEXIBLE CABLE FOR LIFT & OTHER
FLEXIBLE CONNECTIONS
IS-4289/84 PART-I/BS-6977/OTIS-03
6. ARC WELDING CABLE IS-9857/81/BS-638
7. FLEXIBLE CABLE FOR MINERS’ CAP LAMP IS-2593/84
8. RAILWAY CABLES E14/01 (PART-I)/E14/01 (PART-II)
9. SHIP WIRING CABLES DEF STAN 525, 526, 527 SERIES
10. FS CABLE BS-7846/NEK-606
11 OFF SHORE CABLES BS-6883/BS-7917
PURPOSE : TO IDENTIFY THE CABLES AGAINST SPECIFICATION.
20/36
21/36
PURPOSE :TO IDENTIFY THE COMPOUNDS AGAINST SPECIFICATIONS
GOVERNING SPECIFICATIONS OF RUBBER COMPOUNDS
RUBBER COMPOUND GOVERNING SPECIFICATIONS
1. EPR (INSULATION) : IS-6380,IE-2,IE-3,BS-6899,GP-7,DIN-VDE-0207 PT-21,3G13(E11)EI-4
2. CSP (INSULATION) : E-14/01 PT-I,CLW-ES/C-41,41A,IS-6380,IE-4,BS-6899.
3. SILICONE (INSULATION) : IS-6380,IE-5,SE-5,BS-6899,DIN-VDE-0207 PT-20,2G11(E12)
4.PCP (INSULATION) : IE-4,EM-2
5. EPR (SPECIAL GRADE) :RLY.SPECN. FOR INSULATED CATENARY,EM-2,HEPR
3
6. SEMICON COMPD. :VOLUME RESISTIVITY 1.0X10 OHM-CM MAX. AT 27±±±±2 DEG.C
7. CONDUCTING COMPD. : VOLUME RESISTIVITY 300 OHM CM MAX.AT 27±±±±2 DEG.C
8. PCP (SHEATHING) :IS-6380,SE-3,SE-4,BS-6899,RS-3,RS-4,VDE-0207 PT-21,5GM3
9. CSP (SHEATHING) : ----------------------- DO -----------------------------------------
10.NBR-PVC (SHEATHING) :------------------------ DO -----------------------------------------
11.EVA (SHEATHING ) :SHF-2,ZHFR,L F H,ZHLS,SW-4, (LFH=LIMITED FIRE HAZARD)
ACCORDING TO REQMNT. OF SPEC.DIFFERENT INHOUSE
DEVELOPED FORMULAE ARE AVAILABLE .
21/36
22/36
Raw material for
rubber compounding
Inspection
Storage
Compounding
FAILPASS
REJECTION
Conductor wire rod
INSPECTION
PASS
FAIL
Rejection
Storage
Wire drawing,
Annealing & tinning
Bunching&stranding/Melinex Taping
Insulation on CV
Line
Core Laying
Inner sheathing
Outer sheathing, RPC taping &
curing
Printing & final testing
Packing Despatch
N.C
. Handling S
ystem
Non conform
ity handling system
NO
YES
YES
YES
RUBBER CABLES FLOW CHART
SUMMERY INSTRUMRNTATION CABLE MANUFACTURING
22/36
23/36
METHOD OF MANUFACTURING OF RUBBER POWER CABLE
1)CODUCTOR MAKING = 1ST. STEP= WIRE DRAWING / 2ND.STEP = TINNIG / 3RD. STEP= BUNCHING /4TH.STEP =
STRANDING=MELINEX TAPING = READY FOR CORE MAKING
**2)COMPOUND MAKING =1ST. STEP = WEIGHING OF INGREDIENTS / 2ND. STEP =INTERNAL MIXING /3RD. STEP
=ACCELERATOR MIXING= READY FOR EXTRUSION
3)CONDUCTOR INSULATION = DONE IN EXTRUDER = SPARK TESTING (3 TO 9 KV VOLTAGE) = CORE IS READY FOR
LAYING
4)CORE LAYING = DONE IN LAYING MACHINE WITH COTTON TAPE OVER LAID UP CORE =HIGH VOLTAGE TESTING
= LAID UP CORE IS READY FOR SHEATHING
5)INNERSHEATHING (WHERE REQUIRED) = DONE IN EXTRUDER = READY FOR COTTON/ NYLON THREAD OPEN
BRAIDING = READY FOR OUTERSHEATH
6)OUTERSHEATH =DONE IN EXTRUDER = TAKEN IN TRAY / CYLINDER APPLYING POWDER ON SURFACE OF THE
SHEATH
7)COTTON TAPING = A BINDER OF COTTON TAPE IS APPLIED OVER EXTRUDED CABLE FOR STEAM
CURING/VULCANIZING BY LAPPING PROCESS = READY FOR VULCANIZING
**9)VULCANIZING = DONE IN STEAM CHAMBER AT A CERTAIN STEAM PRESSURE & SPECIFIED HOLDING TIME =
STEAM RELEASED = CABLE CYLINDER IS REMOVED FROM THE CHAMBER
10)DETAPING = THE COTTON IS REMOVED FROM THE CABLE SURFACE BY DETAPING MACHINE. = READY FOR
PRINTING
11)PRINTING = CABLE IS PRINTED BY INKJET PRINTER (NONCONTACT PRINTING) & TAKEN IN A PACKING DRUM
(IT MAY BE WOODEN OR METALLIC) = READY FOR PACKING
DIFFERENT RUBBER/ELASTOMERIC CABLES
23/36
24/36
METHOD OF MANUFACTURING OF RUBBER
INSTRUMENTATION CABLE
CONDUCTOR = GLASS MICA TAPING = INSULATION = SPARK TESTING =
TWISTING = HIGH VOLTAGE TESTING = INDIVIDUAL SHEILDING
(MELINEX/AL./MILAR WITH DRAIN WIRE/NO. PRINTEDMELINEX TAPE) =SPARK
TESTING = OVERALL SHEILDING (MELINEX / AL-MILAR WITH DRAIN WIRE /
MELINEX TAPE ) = HIGH VOLTAGE TESTING/IR VALUE CHECKING/ CR VALUE
CHECKING = INNERSHEATH = MELINEX TAPING = BRIDING ( GI WIRE ) =
MELINEX TAPING =DRAIN WIRE TO BRAID &DRAIN TO DRAIN IR VALUE
CHECKING = SHEATHING = PRINTING = TESTING = PACKING
COMPOUNDING PROCESS :-
1) BATCH PREPARATION
2) INTERNAL MIXING
3) ACCELERATOR MIXING/CURATIVES MIXING
1) BATCH PREPARATION : RAW RUBBER &DIFFERENT CHEMICALS ARE WEIGHED ACCORDING TO
FORMULATION (WHICH IS STANDARDISED INHOUSE ).
2) INTERNAL MIXING : THE WHOLE BATCH IS MIXED IN A KNEADER ( INTERNAL MIXER )
ACCORDING TO THE SEQUENCE OF MIXING EXCEPT ACCELERATOR / CURATIVES.
3) ACCELERATOR MIXING : FOR THE SAFETY OF THE COMPOUND ACCELERATOR IS MIXED IN
OPEN MILL AT LOW TEMPERATURE TO AVOID SCORCHING OF THE COMPOUND.
NOTE : AFTER MAKING THE COMPOUND, CONFORMITY IS ASSURED BY CUROMETER TESTING.
SCORCHING : IMMATURE CURING
24/36
25/36
TYPICAL EXAMPLE OF EPR COMPOUND RAW MATERIALS
EPDM RUBBER = 16.000
MODIFIER = 1.800
HEAT STABILISER = 1.000
ANTIOXIDANT(I) = 0.240
ANTIOXIDANT(II) = 0.160
INTERNAL LUBRICANT = 1.000
FILLER = 18.800
PROCESS OIL = 2.600
PROCESS AID = 0.160
COUPLING AGENT = 0.600
ACCELERATOR = 0.600
ACC. ACTIVATOR = 0.300
ITEM DOSES
IN THE MATERIAL SPEC. WE HAVE SEEN DIFFERENT TYPES OF RUBBER COMPOUNDS. NOW WE WILL SEE THE TYPICAL CHEMICALS USED FOR THOSE COMPOUNDS.
MACHINE USED IN RUBBER COMPOUNDING
1) WEIGHING MACHINE:-RANGE :5Kg.-200Kg.
2) INTERNAL MIXER :- a) KNEADER (35 Lit.- 300 Lit.)
b) BANBURY INTERMIX (35 Lit.-300 Lit.)
3) TWO ROLL MILL:- SIZE :14”X42” TO 22”X60”.
25/36
26/36
WHAT IS CURING OR VULCANIZATION PROCESS ?
#CURING/VULCANIZATION IS A PROCESS BY WHICH RUBBER COMPOUNDS GET DIMENSIONAL STABILITY. FOR WHICH A CURING SYSTEM (CURATIVES) IS TO BE INCORPORATED IN THE COMPOUNDING STAGE. WITH THIS CURING SYSTEM THE EXTRUDED COMPOUND GOT CROSSLINKED IN THE MATRIX IN PRESENCE OF HEAT. AS A RESULT OF THAT IT GETS DIMENSIONAL STABILITY.
WHY IS VULCANIZATION REQUIRED ?
#RUBBER IS A VISCO-ELASTIC MATERIAL. IT HAS PROPERTIES OF BOTH VISCOSITY AND ELASTICITY (TO SOME EXTENT). BY VULCANIZATION RUBBER IS CHANGED TO ELASTIC MATERIAL DUE TO CROSS-LINKING.
WHAT IS CV /CCV CURING ?
#CV MEANS CONTINUOUS VULCANIZATION. IT IS A PROCESS BY WHICH EXTRUSION &VULCANIZATION IS DONE AT A TIME. THE WHOLE PROCESS IS CONTINUOUS. BY WHICH WE GET A SMOOTH FINISHED CABLE. HEAT TRANSFER MEDIA IS STEAM.
WHAT IS BATCH CURING ?
#IN THIS PROCESS CABLE IS EXTRUDED OFF LINE . THEN A LAYER OF COTTON TAPE IS APPLIED OVER THE SHEATH AS A BINDER TO PROTECT THE CABLE FROM BLISTERING DURING VULCANIZATION. AT A CERTAIN STEAM PRESSURE THE CABLE WHICH IS TAKEN IN CYLINDER OR TRAY IS HOLD FOR A CERTAIN TIME (e.g. at 3kg Steam Pressure & 45mins. Holding Time) IN A VULCANIZING CHAMBER. AFTER SPECIFIED HOLDING TIME THE STEAM IS RELEASED FROM THE CHAMBER. AFTER THAT THE CABLE IS REMOVED FROM THE CHAMBER. THEN THE COTTON TAPE IS REMOVED BY DETAPING MACHINE.
ABOUT VULCANIZATION PROCESS.FOR RUBBER CABLE VULCANIZATION PART IS VERY VERY IMPORTANT
BATCH CURING CV/CCV CURING
*FOR HIGHER DIA. OF CABLE *FOR LOWER DIA OF CABLE
a) INSULATED CORE = DIA OVER 30MM a) INSULATED CORE = DIA BELOW 30 MM
b) SHEATHED CABLE =DIA OVER 40 MM b) SHEATHED CABLE =DIA BELOW 40MM
UPTO 100 MM (IN CV LINE)
SHEATHED CABLE =DIA UPTO 40 MM.
(IN CCV LINE)
c) FOR PROCESSING OF SHORTER LENGTH C) FOR PROCESSING OF LONGER LENGTH IS
d) IN BATCH PROCESS EXTRUSION IS DONE d) IN CV / CCV LINE EXTRUSION & CURING
OFF LINE FOLLOWED BY TAPING. IS DONE AT A TIME USING STEAM .
e) TAPE IMPRESSION ON CABLE SURFACE e) SMOOTH FINISH ON CABLE SURFACE
MERITS & DEMERITS OVER BATCH CURING & CV CURING.
26/36
27/36
CROSSLINKING BY ELECTRON BEAM :-
THE CHEMICAL EFFECTS OF SUBJECTING A MATERIAL TO AN
ELECTRON BEAM CAN BE TRACED TO A PHENOMENON KNOWN AS IONIZATION.
IONIZATION OCCURS IN MOLECULES SUCH AS HYDROCARBONS. HIGH ENERGY ELECTRONS GIVE UP
THEIR ENERGY TO ATOMS IN THE MOLECULE, BREAKING THE CARBON-HYDROGEN LINKS.CROSSLINKING OCCURS
THEN BY C-C BONDING.
Cross linking by Electron beam
The cross-linking of polymers through electron beam processing changes a thermoplastic
material into a thermo set. When polymers are cross linked, the molecular movement is
severely impeded, making the polymer stable against heat. This locking together of molecules
is the origin of all of the benefits of cross linking, including the improvement of the following
properties: [6]
• Thermal: resistance to temperature, aging, low temperature impact, etc.
• Mechanical: tensile strength, modulus, abrasion resistance, pressure rating, creep
resistance, etc.
• Chemical: stress crack resistance, etc.
• Other: heat shrink memory properties, positive temperature coefficient, etc.
Cross-Linking is the interconnection of adjacent long molecules with networks of bonds
induced by chemical treatment or Electron Beam treatment. Electron Beam processing of
thermoplastic material results in an array of enhancements, such as an increase in tensile
strength, and resistance to abrasions, stress cracking and solvents. Joint replacements such as
knees and hips are being manufactured from Cross-Linked Polyethylene because of the
excellent wear characteristics.
Polymers which are commonly cross linked using the electron beam irradiation process
include polyvinyl chloride (PVC), thermoplastic polyurethanes and elastomers (TPUs),
polybutylene terephthalate (PBT), polyamides / nylon (PA66, PA6, PA11, PA12),
polyvinylidene fluoride (PVDF), polymethylpentene (PMP), polyethylene’s (LLDPE, LDPE,
MDPE, HDPE, UHMWPE), and ethylene copolymers such as ethylene-vinyl acetate (EVA)
and ethylene tetrafluoroethylene (ETFE). Some of the polymers utilize additives to make the
polymer more readily irradiation crosslinkable.
Cross-linked polyethylene piping called PEX is commonly used as an alternative to copper
piping for water lines in newer home construction. PEX piping will outlast copper and has
performance characteristics that are superior to copper in many ways.
27/36
28/36
PROPERTIES OF DIFFERENT RUBBERS/ELASTOMERS 28/36
CHLOROSULPHONATED POLYETHYLENE:
Fast to light , colour fast , flame resistant , good dielectric strength ,particularly recommended for exposure to sunlight , ozone , weather and oxidizing , chemicals , however , it has a very low tensile strength.
INTERNATIONAL NAME: CSM Hardness available: 50-95 shore A RESISTANCE TO TEMPERATURES: -16 C up to +120c SHORT-TIME PEAK TEMPERATURE:- UP TO +175c TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 180(18) TENSILE ELONGATION IN %: 300 properties: ABRASION: Moderate RESISTANCE TO FLEX CRACKING: good TENSILE STRENGTH: good FLEXIBILITY: good STRENGTH OF STRUCTURE: excellent RESISTANCE TO LIGHT: good RESISTANCE TO OXIDIZING: excellent RESISTANCE TO OZONE: excellent RESISTANCE TO WEAR AND TEAR: good WEATHERING EFFECT: excellent RESISTANCE TO: LYES: very good PETROL: moderate BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: moderate SOLVENTS,AROMATIC: moderate SOLVENTS,HALOGENE: moderate OILS AND GREASES: good ACIDS: very good WATER: good
ACRYLONITRILE BUTADINE RUBBER:
Highly resistant to abrasion and tearing. , particularly resistant to ageing. Particularly recommended for crude oil .products, high temperatures, heating and lubricating oils, petrol and paraffin oil.
INTERNATIONAL NAME: NBR Hardness available: 25-95 shore A RESISTANCE TO TEMPERATURES: -10c to +140c SHORT-TIME PEAK TEMPERATURE:- UP TO +160C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 250(25) TENSILE ELONGATION IN %: 500 properties: ABRASION: very good
29/36
RESISTANCE TO FLEX CRACKING: moderate TENSILE STRENGTH: good FLEXIBILITY: good STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: bad RESISTANCE TO OXIDIZING: moderate RESISTANCE TO OZONE: moderate RESISTANCE TO WEAR AND TEAR: very good WEATHERING EFFECT: moderate RESISTANCE TO: LYES: good PETROL: excellent BENZOLE: bad FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: very good SOLVENTS,AROMATIC: conditional SOLVENTS,HALOGENE: bad OILS AND GREASES: excellent ACIDS: conditional WATER: good
CHLOROPRENE RUBBER:
All purpose synthetic rubber, flame resistant, resistant to abrasion, very robust, good dielectric strength, particularly recommended for exposure to ozone and weathering.
INTERNATIONAL NAME: CR Hardness available: 30-90 shore A RESISTANCE TO TEMPERATURES: -40c to +120c SHORT-TIME PEAK TEMPERATURE:- UP TO +150C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 50(25) TENSILE ELONGATION IN %: 450 properties: ABRASION: good RESISTANCE TO FLEX CRACKING: very good TENSILE STRENGTH: good FLEXIBILITY: good STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: very good RESISTANCE TO OXIDIZING: good RESISTANCE TO OZONE: very good RESISTANCE TO WEAR AND TEAR: very good WEATHERING EFFECT: very good RESISTANCE TO: LYES: very good PETROL: moderate BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: moderate SOLVENTS,AROMATIC: moderate SOLVENTS,HALOGENE: bad OILS AND GREASES: good ACIDS: good WATER: very good 29/36
30/36
30/36
STYRENE BUTADINE RUBBER:
Similar to natural rubber, resistant to abrasion, rubbing in good resistance to high temperatures and cracking, resistance to extreme low temperatures, not resistant to petrol, benzene, greases and oils...
INTERNATIONAL NAME: SBR Hardness available: 35-95 shore A RESISTANCE TO TEMPERATURES: -49c to +110c SHORT-TIME PEAK TEMPERATURE:- UP TO +150C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 250(25) TENSILE ELONGATION IN %: 450 properties: ABRASION: very good RESISTANCE TO FLEX CRACKING: good TENSILE STRENGTH: good FLEXIBILITY: good STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: moderate RESISTANCE TO OXIDIZING: moderate RESISTANCE TO OZONE: moderate RESISTANCE TO WEAR AND TEAR: very good WEATHERING EFFECT: good RESISTANCE TO: LYES: good PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: not suitable ACIDS: conditional WATER: very good
EPDM (ETHYLENE PROPYLENE DIENE-RUBBER)
Versatile in use , very good flexibility , resistant to abrasion , resistant to wear and tear ,ozone and weather , low temperatures , can be used to protect against, washing , spraying agents , excellent for profile cords not usable in conjunction with petrol , solvents and mineral oils.
INTERNATIONAL NAME: EPDM/EPM Hardness available: 30-90 shore A RESISTANCE TO TEMPERATURES: -55c up to +150c SHORT-TIME PEAK TEMPERATURE:- -UP TO +180c TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 200(20) TENSILE ELONGATION IN %: 450 properties: ABRASION: good
31/36
RESISTANCE TO FLEX CRACKING: very good TENSILE STRENGTH: good FLEXIBILITY: good STRENGTH OF STRUCTURE: moderate RESISTANCE TO LIGHT: excellent RESISTANCE TO OXIDIZING: excellent RESISTANCE TO OZONE: excellent RESISTANCE TO WEAR AND TEAR: good WEATHERING EFFECT: excellent RESISTANCE TO: LYES: excellent PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: bad SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: bad ACIDS: very good WATER: very good
SILICONE RUBBER: 31/36
Resistant to high temperature ,odourless and tasteless , nontoxic , can be sterilized in accordance with foodstuffs regulations ,, resistant to sea water and corrosive salt solutions , not to be used in conjunction with steam water concentrated acids and lies , swells. Strongly under the effect of aromatic solvents.
INTERNATIONAL NAME: MVQ/SI Hardness available: 40-80 shore A RESISTANCE TO TEMPERATURES: -70c up to +180c SHORT-TIME PEAK TEMPERATURE:- UP TO +225c TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 80(8) TENSILE ELONGATION IN %: 250 properties: ABRASION: Moderate RESISTANCE TO FLEX CRACKING: bad TENSILE STRENGTH: bad FLEXIBILITY: good STRENGTH OF STRUCTURE: moderate RESISTANCE TO LIGHT: excellent RESISTANCE TO OXIDIZING: very good RESISTANCE TO OZONE: excellent RESISTANCE TO WEAR AND TEAR: bad WEATHERING EFFECT: excellent RESISTANCE TO: LYES: not suitable PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: excellently suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: good ACIDS: not suitable WATER: good
32/36
32/36
NATURAL RUBBER:
Characterized by flexibility strength and low temperature resistance as well as excellent physical properties ideal for bonded rubber/metal elements. Not suitable for petreol, grease, oils and ozone.
INTERNATIONAL NAME: NR Hardness available: 25-95 shore A RESISTANCE TO TEMPERATURES: -40c to +80c SHORT-TIME PEAK TEMPERATURE:- +100C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 250(25) TENSILE ELONGATION IN %: 800 properties: ABRASION: good RESISTANCE TO FLEX CRACKING: good TENSILE STRENGTH: excellent FLEXIBILITY: excellent STRENGTH OF STRUCTURE: excellent RESISTANCE TO LIGHT: bad RESISTANCE TO OXIDIZING: moderate RESISTANCE TO OZONE: moderate RESISTANCE TO WEAR AND TEAR: very good WEATHERING EFFECT: good RESISTANCE TO: LYES: good PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: not suitable ACIDS: conditional WATER: good
ACRYLIC RUBBER:
Good resistance to high temperature and mineraloils, high resistance to oxygen low -temperature properties.
INTERNATIONAL NAME: ACM Hardness available: 50-80 shore A RESISTANCE TO TEMPERATURES: - 35c to +175c SHORT-TIME PEAK TEMPERATURE:- +200C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 160(16) TENSILE ELONGATION IN %: up to 350 properties:
33/36
ABRASION: Moderate RESISTANCE TO FLEX CRACKING: Moderate TENSILE STRENGTH: good FLEXIBILITY: OF low STRENGTH OF STRUCTURE: - RESISTANCE TO LIGHT: good RESISTANCE TO OXIDIZING: very good RESISTANCE TO OZONE: very good RESISTANCE TO WEAR AND TEAR: good WEATHERING EFFECT: very good RESISTANCE TO: LYES: not suitable PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: not suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: bad SOLVENTS,HALOGENE: bad OILS AND GREASES: very good ACIDS: not suitable WATER:
FLUORINATED RUBBER (VITON):
Hexafluoroprppylene . Vinylidene fluoride. Copolymer.Resistant to extreme temperature even over 200c .Very good mechanical properties and high resistance to tearing even at high temperatures .Excellent for exposure to sunlight, ozone and weather .Not recommended for use in conjunction with esters and ketones.
INTERNATIONAL NAME: FPM Hardness available: 60-90 shore A RESISTANCE TO TEMPERATURES: -30c up to +225c SHORT-TIME PEAK TEMPERATURE:- UP TO +350c TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 200(20) TENSILE ELONGATION IN %: 400 properties: ABRASION: Moderate RESISTANCE TO FLEX CRACKING: good TENSILE STRENGTH: good FLEXIBILITY: moderate STRENGTH OF STRUCTURE: almost good RESISTANCE TO LIGHT: excellent RESISTANCE TO OXIDIZING: excellent RESISTANCE TO OZONE: excellent RESISTANCE TO WEAR AND TEAR: almost good WEATHERING EFFECT: excellent RESISTANCE TO: LYES: very good PETROL: excellent BENZOLE: good FOOD STUFFS: not suitable SOLVENTS,ALIPHATIC: very good SOLVENTS,AROMATIC: good SOLVENTS,HALOGENE: good OILS AND GREASES: good ACIDS: very good WATER:
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POLYBORON RUBBER 34/36
High mechanical strength, good resistance to ozone medium resistance to oil flexibility\damping property can be varied as required. Excellent resistance to water\, slight permanent set.
INTERNATIONAL NAME: PNR Hardness available: 10-80 shore A RESISTANCE TO TEMPERATURES: -30c to +80c SHORT-TIME PEAK TEMPERATURE:- +100C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 170(17) TENSILE ELONGATION IN %: 300 TO 700 properties: ABRASION: good RESISTANCE TO FLEX CRACKING: moderate TENSILE STRENGTH: good FLEXIBILITY: as required STRENGTH OF STRUCTURE: moderate RESISTANCE TO LIGHT: good RESISTANCE TO OXIDIZING: good RESISTANCE TO OZONE: good RESISTANCE TO WEAR AND TEAR: good WEATHERING EFFECT: good RESISTANCE TO: LYES: moderate PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: not suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: conditional ACIDS: moderate WATER: excellent
EPICHLOROHYDRIN RUBBER:
Low gas permeability, very good low temperature properties, good resistance to mineral oils ozone and high temperature
INTERNATIONAL NAME: eco Hardness available: 50-90 shore A RESISTANCE TO TEMPERATURES: -40c to +130c SHORT-TIME PEAK TEMPERATURE:- +150C TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 170(17)
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TENSILE ELONGATION IN %: 150 TO 500 properties: ABRASION: moderate RESISTANCE TO FLEX CRACKING: good TENSILE STRENGTH: good FLEXIBILITY: moderate STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: good RESISTANCE TO OXIDIZING: good RESISTANCE TO OZONE: very good RESISTANCE TO WEAR AND TEAR: - WEATHERING EFFECT: good RESISTANCE TO: LYES: bad PETROL: good BENZOLE: good FOOD STUFFS: not suitable SOLVENTS,ALIPHATIC: good SOLVENTS,AROMATIC: good SOLVENTS,HALOGENE: not suitable OILS AND GREASES: very good ACIDS: moderate WATER: m
BUTYL RUBBER: 35/36
Very slightly permeable to air, steam and other gases ,good resistance to heat, oxygen, ozone and many chemicals and solvents, good electrical properties(isolating),good resistance to abrasion and tear propagation.
INTERNATIONAL NAME: IIR Hardness available: 45-85 shore A RESISTANCE TO TEMPERATURES: -40c to +130c SHORT-TIME PEAK TEMPERATURE:- +150 TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 170(17) TENSILE ELONGATION IN %: 400 to 800 properties: ABRASION: good RESISTANCE TO FLEX CRACKING: moderate TENSILE STRENGTH: good FLEXIBILITY: slight STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: very good RESISTANCE TO OXIDIZING: very good RESISTANCE TO OZONE: very good RESISTANCE TO WEAR AND TEAR: - WEATHERING EFFECT: very good RESISTANCE TO: LYES: very good PETROL: not suitable BENZOLE: not suitable FOOD STUFFS: suitable SOLVENTS,ALIPHATIC: not suitable SOLVENTS,AROMATIC: not suitable SOLVENTS,HALOGENE: not suitable OILS AND GREASES: not suitable ACIDS: very good WATER:
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HYDROGENATED NBR:
High resistance to heat, ozone and oil, good mechanical properties also at high temperatures, excellent resistance to wear and tear...
INTERNATIONAL NAME: HNBR Hardness available: 40-90 shore A RESISTANCE TO TEMPERATURES: -25c to +175c SHORT-TIME PEAK TEMPERATURE:- +200c TENSILE STRENGTHIN KP\SQ.CM(N\SQ.MM): 300(30) TENSILE ELONGATION IN %: 150 to 600 properties: ABRASION: very good RESISTANCE TO FLEX CRACKING: very good TENSILE STRENGTH: very good FLEXIBILITY: good STRENGTH OF STRUCTURE: good RESISTANCE TO LIGHT: good RESISTANCE TO OXIDIZING: good RESISTANCE TO OZONE: good RESISTANCE TO WEAR AND TEAR: good WEATHERING EFFECT: good RESISTANCE TO: LYES: good PETROL: good BENZOLE: moderate FOOD STUFFS: not suitable SOLVENTS,ALIPHATIC: very good SOLVENTS,AROMATIC: conditional SOLVENTS,HALOGENE: conditional OILS AND GREASES: very good ACIDS: moderate(conditional) WATER:
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