Difference between revisions of "Elastomer" - New World Encyclopedia

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[[Image:Nascarphx16.jpg|thumb|right|250px|Rubber, an elastomer, is widely used for the manufacture of tires.]]
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[[Image:Chips TPU con eurocent.jpg|thumb|200px|Chips of thermoplastic polyurethane.]]
  
An '''elastomer''' is a [[polymer]] with the property of [[elasticity]]. The term, which is derived from ''elastic polymer'', is often used interchangeably with the term [[rubber]], and is preferred when referring to [[vulcanization|vulcanisates]]. Each of the [[monomer]]s that links to form the polymer is usually made of carbon, hydrogen, oxygen, and/or silicon. Elastomers are [[amorphous polymer]]s existing above their [[glass transition temperature]], so that considerable segmental motion is possible. At [[ambient temperature]]s, rubbers are thus relatively soft ([[Young's modulus|E]]~3MPa) and deformable. Their primary uses are for [[Seal (mechanical)|seal]]s, [[adhesive]]s, and molded flexible parts.
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An '''elastomer''' is a [[polymer]] with the property of [[elasticity]]. In other words, it is a polymer that deforms under stress and returns to its original shape when the stress is removed. The term is a contraction of the words "elastic polymer." There are many types of elastomers, most of which are [[rubber]]s. The term ''elastomer'' is therefore often used interchangeably with the term ''rubber.'' Other elastomers, which melt when heated, are classified as [[thermoplastic]].
  
==Background==
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Rubbers (both natural and [[synthetic]]) are widely used for the manufacture of tires, tubes, hoses, belts, matting, [[glove]]s, toy balloons, [[rubber band]]s, pencil [[eraser]]s, and [[adhesive]]s. Thermoplastic elastomers are used in manufacturing processes, such as by injection molding. Thermoplastic polyurethanes are used for various applications, including the production of foam seating, [[seal (device)|seal]]s, [[gasket]]s, and [[carpet]] underlay.
[[Image:Polymer picture.PNG|frame|A is a schematic drawing of an unstressed polymer. B is the same polymer under stress. When the stress is removed, it will return to the A configuration. (The dots represent cross-links.)]]
 
  
Elastomers are usually [[thermoset]]s (requiring [[vulcanization]]) but may also be [[thermoplastic]] (see [[thermoplastic elastomer]]).  The long polymer chains [[cross-link]] during curing. The molecular structure of elastomers can be imagined as a 'spaghetti and meatball' structure, with the meatballs signifying cross-links. The elasticity is derived from the ability of the long chains to reconfigure themselves to distribute an applied stress. The covalent cross-linkages ensure that the elastomer will return to its original configuration when the stress is removed. As a result of this extreme flexibility, elastomers can reversibly extend from 5-700%, depending on the specific material. Without the cross-linkages or with short, uneasily reconfigured chains, the applied stress would result in a permanent deformation.
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== Properties ==
  
Temperature effects are also present in the demonstrated elasticity of a polymer. Elastomers that have cooled to a glassy or crystalline phase will have less mobile chains, and consequentially less elasticity, than those manipulated at temperatures higher than the glass transition temperature of the polymer.
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Elastomers are [[amorphous polymer]]s with considerable segmental motion. Their general molecular form has been likened to a "spaghetti and meatball" structure, where the meatballs signify [[cross-link]]s between the flexible [[polymer]] chains, which are like spaghetti strands. Each polymer chain is made up of many [[monomer]] subunits, and each monomer is usually made of carbon, hydrogen, and oxygen atoms, and occasionally silicon atoms.
  
It is also possible for a polymer to exhibit elasticity that is not due to covalent cross-links, but instead for  [[Thermodynamic theory of polymer elasticity|thermodynamic reasons]].
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Most elastomers are [[thermoset]]s—that is, they require curing (by [[heat]], [[chemical reaction]], or [[irradiation]]). In the curing process, the long polymer chains become [[cross-link]]ed by [[covalent bond]]s, the material becomes stronger, and it cannot be remelted and remolded. Some elastomers are thermoplastic, melting to a liquid state when heated and turning brittle when cooled sufficiently. In thermoplastic elastomers, the polymer chains are cross-linked by weaker bonds, such as [[hydrogen bond]]s or [[Intermolecular force|dipole-dipole]] interactions.
  
==Mathematic justifications==
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The elasticity is derived from the ability of the long chains to reconfigure themselves to distribute an applied stress. Covalent cross-linkages, in particular, ensure that the elastomer will return to its original configuration when the stress is removed. As a result of this extreme flexibility, elastomers can reversibly extend from 5 to 700 percent, depending on the specific material. Without the cross-linkages or with short, uneasily reconfigured chains, the applied stress would result in permanent deformation.
  
Using the laws of thermodynamics, stress definitions and polymer characteristics (complete derivation in [1], pages103-105), we find ideal stress behavior:
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The temperature of the polymer also affects its elasticity. Elastomers that have been cooled to a glassy or crystalline phase will have less mobile chains, and consequently less elasticity, than those manipulated at temperatures higher than the glass transition temperature of the polymer. At [[ambient temperature]]s, rubbers are thus relatively soft ([[Young's modulus]] of about 3 MPa) and deformable.
 
 
<math> \sigma\ = n k T [ \lambda\ _ 1 ^ 2 + \lambda\ _ 1 ^ {-1} ] </math>
 
 
 
where <math>n</math> is the number of chain segments per unit volume, <math>k</math> is [[Boltzmann's Constant]], <math>T</math> is temperature, and <math> \lambda\ _ 1 </math> is distortion in the 1 direction.
 
 
 
These findings are accurate for values of up to approximately 400% strain. At this point, alignment between stretched chains begins to result in crystallization from [[noncovalent bonding]].
 
 
 
While [[Young's Modulus]] does not exist for elastomers due to the nonlinear nature of the stress-strain relationship, a "secant modulus" can be found at a particular strain.
 
  
 
==Examples of elastomers==
 
==Examples of elastomers==
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Saturated Rubbers that cannot be cured by sulfur vulcanization:
 
Saturated Rubbers that cannot be cured by sulfur vulcanization:
*EPM ('''[[ethylene propylene rubber]]''', a copolymer of [[ethylene]] and [[propylene]]) and [[EPDM rubber]] ('''ethylene propylene diene rubber''', a terpolymer of ethylene, propylene and a [[diene]]-component)
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*EPM ('''[[ethylene propylene rubber]],''' a copolymer of [[ethylene]] and [[propylene]]) and [[EPDM rubber]] ('''ethylene propylene diene rubber''' a terpolymer of ethylene, propylene and a [[diene]]-component)
 
*[[Epichlorohydrin]] rubber (ECO)
 
*[[Epichlorohydrin]] rubber (ECO)
 
*Polyacrylic rubber (ACM, ABR)
 
*Polyacrylic rubber (ACM, ABR)
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*The [[protein]]s [[resilin]] and [[elastin]]
 
*The [[protein]]s [[resilin]] and [[elastin]]
 
*[[Polysulfide]] Rubber
 
*[[Polysulfide]] Rubber
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== Uses ==
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Most elastomers are rubbers, including both natural and synthetic varieties. They are used mainly for the manufacture of tires and tubes. They are also used to produce goods such as hoses, belts, matting, [[glove]]s, toy balloons, [[rubber band]]s, [[pencil]] [[eraser]]s, and [[adhesive]]s. As a fiber, rubber (called "elastic") is valuable for the textile industry. Ethylene propylene rubber (EPR) is useful as [[electrical insulation|insulation]] for [[high voltage]] [[power cable|cables]]. Thermoplastic elastomers are relatively easy to use in manufacturing processes, such as by injection molding.
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Polyurethanes are widely used in high-resiliency, flexible foam seating, [[seal (device)|seal]]s, [[gasket]]s, [[carpet]] underlay, [[Spandex]] [[Synthetic fibre|fibers]], and electrical potting compounds.
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==Mathematical background==
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Using the laws of thermodynamics, stress definitions, and polymer characteristics,<ref>Treloar 2005.</ref> ideal stress behavior may be calculated using the following equation:
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<math> \sigma\ = n k T [ \lambda\ _ 1 ^ 2 + \lambda\ _ 1 ^ {-1} ] </math>
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 +
where <math>n</math> is the number of chain segments per unit volume, <math>k</math> is [[Boltzmann's Constant]], <math>T</math> is temperature, and <math> \lambda\ _ 1 </math> is distortion in the 1 direction.
 +
 +
These findings are accurate for values up to approximately 400 percent strain. At that point, alignment between stretched chains begins to result in crystallization from [[noncovalent bonding]].
 +
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Although [[Young's Modulus]] does not exist for elastomers because of the nonlinear nature of the stress-strain relationship, a "secant modulus" can be found at a particular strain.
  
 
== See also ==
 
== See also ==
  
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* [[Ethylene]]
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* [[Isoprene]]
 
* [[Polymer]]
 
* [[Polymer]]
 
* [[Rubber]]
 
* [[Rubber]]
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== Notes ==
 +
<references/>
  
 
==References==
 
==References==
 
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*Budinski, Kenneth G., and Michael K. Budinski. ''Engineering Materials: Properties and Selection.''  Prentice Hall College Div. 7th ed. 2002.  ISBN 0130305332.
* Treloar, L.R.G. ''The Physics of Rubber Elasticity''. Oxford University Press, 1975. ISBN 019850279.
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* Mark, James E., Burak Erman, and Frederick R. Eirich (eds.). ''Science and Technology of Rubber,'' 3rd edition. Amsterdam: Elsevier Academic Press, 2005. ISBN 978-0124647862.
 
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* Meyers, Marc A., and Krishan Kumar Chawla. ''Mechanical Behavior of Materials.'' San Diego: M. Meyers, 2007. ISBN 978-1427614827.
*Meyers and Chawla. '''Mechanical Behaviors of Materials''', Prentice Hall, Inc. (Pearson Education) 1999.
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* Treloar, L.R.G. ''The Physics of Rubber Elasticity.'' Oxford: Clarendon Press. 3rd ed. 2005. ISBN 978-0198570271.
 
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* Ward, I.M., and J. Sweeney. ''An Introduction to the Mechanical Properties of Solid Polymers.'' Chichester, West Sussex, UK: Wiley, 2004. ISBN 978-0471496267.
*Budinski, Kenneth G., Budinski, Michael K., ''Engineering Materials: Properties and Selection'', 7th Ed, 2002. ISBN 0-13-030533-2.
 
  
 
[[Category:Physical sciences]]
 
[[Category:Physical sciences]]

Latest revision as of 07:38, 10 August 2023

Rubber, an elastomer, is widely used for the manufacture of tires.
Chips of thermoplastic polyurethane.

An elastomer is a polymer with the property of elasticity. In other words, it is a polymer that deforms under stress and returns to its original shape when the stress is removed. The term is a contraction of the words "elastic polymer." There are many types of elastomers, most of which are rubbers. The term elastomer is therefore often used interchangeably with the term rubber. Other elastomers, which melt when heated, are classified as thermoplastic.

Rubbers (both natural and synthetic) are widely used for the manufacture of tires, tubes, hoses, belts, matting, gloves, toy balloons, rubber bands, pencil erasers, and adhesives. Thermoplastic elastomers are used in manufacturing processes, such as by injection molding. Thermoplastic polyurethanes are used for various applications, including the production of foam seating, seals, gaskets, and carpet underlay.

Properties

Elastomers are amorphous polymers with considerable segmental motion. Their general molecular form has been likened to a "spaghetti and meatball" structure, where the meatballs signify cross-links between the flexible polymer chains, which are like spaghetti strands. Each polymer chain is made up of many monomer subunits, and each monomer is usually made of carbon, hydrogen, and oxygen atoms, and occasionally silicon atoms.

Most elastomers are thermosets—that is, they require curing (by heat, chemical reaction, or irradiation). In the curing process, the long polymer chains become cross-linked by covalent bonds, the material becomes stronger, and it cannot be remelted and remolded. Some elastomers are thermoplastic, melting to a liquid state when heated and turning brittle when cooled sufficiently. In thermoplastic elastomers, the polymer chains are cross-linked by weaker bonds, such as hydrogen bonds or dipole-dipole interactions.

The elasticity is derived from the ability of the long chains to reconfigure themselves to distribute an applied stress. Covalent cross-linkages, in particular, ensure that the elastomer will return to its original configuration when the stress is removed. As a result of this extreme flexibility, elastomers can reversibly extend from 5 to 700 percent, depending on the specific material. Without the cross-linkages or with short, uneasily reconfigured chains, the applied stress would result in permanent deformation.

The temperature of the polymer also affects its elasticity. Elastomers that have been cooled to a glassy or crystalline phase will have less mobile chains, and consequently less elasticity, than those manipulated at temperatures higher than the glass transition temperature of the polymer. At ambient temperatures, rubbers are thus relatively soft (Young's modulus of about 3 MPa) and deformable.

Examples of elastomers

Unsaturated rubbers that can be cured by sulfur vulcanization:

  • Natural Rubber (NR)
  • Synthetic Polyisoprene (IR)
  • Butyl rubber (copolymer of isobutylene and isoprene, IIR)
    • Halogenated butyl rubbers (Chloro Butyl Rubber: CIIR; Bromo Butyl Rubber: BIIR)
  • Polybutadiene (BR)
  • Styrene-butadiene Rubber (copolymer of polystyrene and polybutadiene, SBR)
  • Nitrile Rubber (copolymer of polybutadiene and acrylonitrile, NBR), also called Buna N rubbers
    • Hydrogenated Nitrile Rubbers (HNBR) Therban and Zetpol
  • Chloroprene Rubber (CR), polychloroprene, Neoprene, Baypren etc.

(Note that unsaturated rubbers can also be cured by non-sulfur vulcanization if desired).

Saturated Rubbers that cannot be cured by sulfur vulcanization:

  • EPM (ethylene propylene rubber, a copolymer of ethylene and propylene) and EPDM rubber (ethylene propylene diene rubber a terpolymer of ethylene, propylene and a diene-component)
  • Epichlorohydrin rubber (ECO)
  • Polyacrylic rubber (ACM, ABR)
  • Silicone rubber (SI, Q, VMQ)
  • Fluorosilicone Rubber (FVMQ)
  • Fluoroelastomers (FKM, and FEPM) Viton, Tecnoflon, Fluorel, Aflas and Dai-El
  • Perfluoroelastomers (FFKM) Tecnoflon PFR, Kalrez, Chemraz, Perlast
  • Polyether Block Amides (PEBA)
  • Chlorosulfonated Polyethylene (CSM), (Hypalon)
  • Ethylene-vinyl acetate (EVA)

Various other types of elastomers:

  • Thermoplastic elastomers (TPE), for example Elastron, etc.
  • Thermoplastic Vulcanizates (TPV), for example Santoprene TPV
  • Thermoplastic Polyurethane (TPU)
  • Thermoplastic Olefins (TPO)
  • The proteins resilin and elastin
  • Polysulfide Rubber

Uses

Most elastomers are rubbers, including both natural and synthetic varieties. They are used mainly for the manufacture of tires and tubes. They are also used to produce goods such as hoses, belts, matting, gloves, toy balloons, rubber bands, pencil erasers, and adhesives. As a fiber, rubber (called "elastic") is valuable for the textile industry. Ethylene propylene rubber (EPR) is useful as insulation for high voltage cables. Thermoplastic elastomers are relatively easy to use in manufacturing processes, such as by injection molding.

Polyurethanes are widely used in high-resiliency, flexible foam seating, seals, gaskets, carpet underlay, Spandex fibers, and electrical potting compounds.

Mathematical background

Using the laws of thermodynamics, stress definitions, and polymer characteristics,[1] ideal stress behavior may be calculated using the following equation:

where is the number of chain segments per unit volume, is Boltzmann's Constant, is temperature, and is distortion in the 1 direction.

These findings are accurate for values up to approximately 400 percent strain. At that point, alignment between stretched chains begins to result in crystallization from noncovalent bonding.

Although Young's Modulus does not exist for elastomers because of the nonlinear nature of the stress-strain relationship, a "secant modulus" can be found at a particular strain.

See also

Notes

  1. Treloar 2005.

References
ISBN links support NWE through referral fees

  • Budinski, Kenneth G., and Michael K. Budinski. Engineering Materials: Properties and Selection. Prentice Hall College Div. 7th ed. 2002. ISBN 0130305332.
  • Mark, James E., Burak Erman, and Frederick R. Eirich (eds.). Science and Technology of Rubber, 3rd edition. Amsterdam: Elsevier Academic Press, 2005. ISBN 978-0124647862.
  • Meyers, Marc A., and Krishan Kumar Chawla. Mechanical Behavior of Materials. San Diego: M. Meyers, 2007. ISBN 978-1427614827.
  • Treloar, L.R.G. The Physics of Rubber Elasticity. Oxford: Clarendon Press. 3rd ed. 2005. ISBN 978-0198570271.
  • Ward, I.M., and J. Sweeney. An Introduction to the Mechanical Properties of Solid Polymers. Chichester, West Sussex, UK: Wiley, 2004. ISBN 978-0471496267.

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