Surreal and Thermoplastic: Difference between pages

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{{otheruses2|Plastic}}
A '''thermoplastic''' is a [[plastic]] that [[melt]]s to a liquid when heated and freezes to a [[brittle]], very [[glass]]y state when cooled sufficiently. Most thermoplastics are high-[[molecular mass|molecular-weight]] [[polymer]]s whose [[Chain (sequence)|chain]]s associate through weak [[Van der Waals force]]s ([[polyethylene]]); stronger [[dipole|dipole-dipole]] interactions and [[hydrogen bond]]ing ([[nylon]]); or even stacking of [[aromatic]] rings ([[polystyrene]]). Thermoplastic polymers differ from [[thermosetting plastic|thermosetting]] polymers ([[Bakelite]]; [[vulcanization|vulcanized]] [[rubber]]) as they can, unlike thermosetting polymers, be remelted and remoulded. Many thermoplastic materials are [[addition polymer]]s; e.g., [[vinyl]] chain-growth polymers such as polyethylene and [[polypropylene]].

The difference between thermoplastics and [[thermosetting]] plastics is that thermoplastics become soft, remoldable and weldable when heat is added. Thermosetting plastics however, when heated will chemically decompose, so they can not be welded or remolded. On the other hand, once a thermosetting is cured it tends to be stronger than a thermoplastic.

==Temperature dependence==
[[Image:Tempdependence.jpg|thumb|Stress strain graph of thermoplastic material.]]
Thermoplastics are elastic and flexible above a [[glass transition temperature]] ''T''<sub>g</sub>, specific for each one — the midpoint of a [[temperature]] range in contrast to the sharp [[melting point]]
and [[freezing point]] of a pure [[crystal]]line substance like [[water]]. Below a second, higher melting temperature, ''T''<sub>m</sub>, also the midpoint of a range, most thermoplastics have crystalline regions alternating with [[amorphous solid|amorphous]] regions in which the chains approximate [[random coil]]s. The amorphous regions contribute [[Hooke's law|elasticity]] and the crystalline regions contribute strength and rigidity, as is also the case for non-thermoplastic [[fibrous protein]]s such as [[silk]]. (Elasticity does not mean they are particularly stretchy; e.g., nylon [[rope]] and [[fishing line]].) Above ''T''<sub>m</sub> all crystalline structure disappears and the chains become randomly inter dispersed. As the temperature increases above ''T''<sub>m</sub>, [[viscosity]] gradually decreases without any distinct [[phase (matter)|phase]] change.

Thermoplastics can go through melting/freezing cycles repeatedly and the fact that they can be reshaped upon reheating gives them their name. This quality makes thermoplastics recyclable. The processes required for recycling vary with the thermoplastic. The plastics used for pop bottles are a common example of thermoplastics that can be and are widely recycled. [[Horn (anatomy)|Animal horn]], made of the [[protein]] [[keratin|α-keratin]], softens on heating, is somewhat reshapable, and may be regarded as a natural, quasi-thermoplastic material.

Some thermoplastics normally do not crystallize: they are termed "amorphous" plastics and are useful at temperatures below the ''T''<sub>g</sub>. They are frequently used in applications where clarity is important. Some typical examples of amorphous thermoplastics are [[PMMA]], [[Polystyrene|PS]] and [[Polycarbonate|PC]]. Generally, amorphous thermoplastics are less chemically resistant and can be subject to [[stress cracking]]. Thermoplastics will crystallize to a certain extent and are called "semi-crystalline" for this reason. Typical semi-crystalline thermoplastics are PE, PP, PBT and PET. The speed and extent to which crystallization can occur depends in part on the flexibility of the polymer chain. Semi-crystalline thermoplastics are more resistant to solvents and other chemicals. If the crystallites are larger than the wavelength of light, the thermoplastic is hazy or opaque.
Semi-crystalline thermoplastics become less brittle above ''T''<sub>g</sub>. If a plastic with otherwise desirable properties has too high a ''T''<sub>g</sub>, it can often be lowered by adding a low-molecular-weight [[plasticizer]] to the melt before forming ([[Plastics extrusion]]; [[molding (process)|molding]]) and cooling. A similar result can sometimes be achieved by adding non-reactive [[side chain]]s to the [[monomer]]s before [[polymerization]]. Both methods make the polymer chains stand off a bit from one another. Before the introduction of plasticizers, [[plastic]] [[automobile]] parts often cracked in cold [[winter]] [[weather]]. Another method of lowering ''T''<sub>g</sub> (or raising ''T''<sub>m</sub>) is to incorporate the original plastic into a [[copolymer]], as with [[graft copolymer]]s of polystyrene, or into a [[composite material]]. Lowering ''T''<sub>g</sub> is not the only way to reduce brittleness. [[Drawing (manufacturing)|Drawing]] (and similar processes that stretch or orient the molecules) or increasing the length of the polymer chains also decrease brittleness.

Although modestly vulcanized natural and synthetic rubbers are stretchy, they are [[elastomer]]ic thermosets, not thermoplastics. Each has its own ''T''<sub>g</sub>, and will crack and shatter when cold enough so that the [[cross-link|crosslinked]] polymer chains can no longer move relative to one another. But they have no ''T''<sub>m</sub> and will decompose at high temperatures rather than melt. Recently, [[thermoplastic elastomer]]s have become available!

==Terminology==
The literature on thermoplastics is huge, and can be quite confusing, as the same chemical can be available in many different forms (for example, at different molecular weights), which might have quite different physical properties. The same chemical can be referred to by many different tradenames, by different abbreviations; two chemical compounds can share the same name; a good example of the latter is the word "Teflon" which is used to refer to a specific polymer (PTFE); to related polymers such as PFA, and generically to [[fluoropolymer]]s.

Furthermore, over the last 30 years, there has been tremendous change in the plastics industry, with many companies going out of business or merging into other companies. Many production plants frequently changed hands or have been relocated to emerging countries in Eastern Europe or Asia, with different trademarks. <!-- Hidden, because too much detailed and inappropriate for the contents of an encyclopedia: e.g., the plastics business of GE, located in central Massachusetts, was acquired by SABIC, Saudi Basic Industries. -->

==Testing==
Testing of thermoplastics can take various forms.

'''Tensile tests''' — ISO 527 -1/-2 and ASTM D 638 set out the standardized test methods. These standards are technically equivalent. However they are not fully comparable because of the difference in testing speeds. The modulus determination requires a high accuracy of ± 1 micrometer for the [[dilatometer]].

'''Flexural tests''' — 3-points flexural tests are among the most common and classic methods for semi rigid and rigid plastics.

'''Pendulum impact tests''' — impact tests are used to measure the behavior of materials at higher deformation speeds. Pendulum impact testers are used to determine the energy required to break a standardized specimen by measuring the height to which the pendulum hammer rises after impacting the test piece.

==List of thermoplastics==
* [[Acrylonitrile butadiene styrene]] (ABS)
* [[Polymethyl methacrylate|Acrylic]] (PMMA)
* [[Celluloid]]
* [[Cellulose acetate]]
* [[Ethylene-Vinyl Acetate]] (EVA)
* [[EVOH|Ethylene vinyl alcohol]] (EVOH)
* [[Fluoropolymer|Fluoroplastics]] (PTFE, alongside with FEP, PFA, CTFE, ECTFE, ETFE)
* [[Ionomer]]s
* [[Kydex]], a trademarked acrylic/PVC [[alloy]]
* [[Liquid Crystal Polymer]] (LCP)
* [[Polyacetal]] (POM or Acetal)
* [[Polymethyl methacrylate|Polyacrylates]] (Acrylic)
* [[Polyacrylonitrile]] (PAN or Acrylonitrile)
* [[Polyamide]] (PA or Nylon)
* [[Polyamide-imide]] (PAI)
* [[Polyaryletherketone]] (PAEK or Ketone)
* [[Polybutadiene]] (PBD)
* [[Polybutylene]] (PB)
* [[Polybutylene terephthalate]] (PBT)
* [[Polycaprolactone]] (PCL)
* [[Polychlorotrifluoroethylene]] (PCTFE)
* [[Polyethylene terephthalate]] (PET)
* [[Polycyclohexylene dimethylene terephthalate]] (PCT)
* [[Polycarbonate]] (PC)
* [[Polyhydroxyalkanoates]] (PHAs)
* [[Polyketone]] (PK)
* [[Polyester]]
* [[Polyethylene]] (PE)
* [[Polyetheretherketone]] (PEEK)
* [[Polyetherimide]] (PEI)
* [[Polyethersulfone]] (PES)- see [[Polysulfone]]
* [[Polyethylenechlorinates]] (PEC)
* [[Polyimide]] (PI)
* [[Polylactic acid]] (PLA)
* [[Polymethylpentene]] (PMP)
* [[Polyphenylene oxide]] (PPO)
* [[Polyphenylene sulfide]] (PPS)
* [[Polyphthalamide]] (PPA)
* [[Polypropylene]] (PP)
* [[Polystyrene]] (PS)
* [[Polysulfone]] (PSU)
* [[Polytrimethylene terephthalate]] (PTT)
* [[Polyurethane]] (PU)
* [[Polyvinyl acetate]] (PVA)
* [[Polyvinyl chloride]] (PVC)
* [[Polyvinylidene chloride]] (PVDC)
* [[Spectralon]]
* [[Styrene-acrylonitrile]] (SAN)

==See also==
*[[Thermosetting plastic]]
*[[Plastic]]
*[[Nurdle]]

==References==
{{Reflist}}

[[Category:Plastics]]
[[Category:Polymer physics]]
[[Category:Thermoplastics]]

[[ar:لدائن حرارية]]
[[ca:Termoplàstic]]
[[cs:Termoplast]]
[[de:Thermoplast]]
[[es:Termoplástico]]
[[fa:ترموپلاستیک]]
[[it:Polimeri termoplastici]]
[[nl:Thermoplast]]
[[pl:Tworzywa termoplastyczne]]
[[pt:Termoplástico]]
[[ru:Термопласты]]
[[simple:Thermoplastic]]
[[sk:Termoplast]]
[[fi:Termoplastinen]]
[[sv:Termoplast]]
[[tr:Termoplastik]]
[[zh:热塑性塑料]]

Revision as of 16:32, 12 October 2008

Template:Otheruses2 A thermoplastic is a plastic that melts to a liquid when heated and freezes to a brittle, very glassy state when cooled sufficiently. Most thermoplastics are high-molecular-weight polymers whose chains associate through weak Van der Waals forces (polyethylene); stronger dipole-dipole interactions and hydrogen bonding (nylon); or even stacking of aromatic rings (polystyrene). Thermoplastic polymers differ from thermosetting polymers (Bakelite; vulcanized rubber) as they can, unlike thermosetting polymers, be remelted and remoulded. Many thermoplastic materials are addition polymers; e.g., vinyl chain-growth polymers such as polyethylene and polypropylene.

The difference between thermoplastics and thermosetting plastics is that thermoplastics become soft, remoldable and weldable when heat is added. Thermosetting plastics however, when heated will chemically decompose, so they can not be welded or remolded. On the other hand, once a thermosetting is cured it tends to be stronger than a thermoplastic.

Temperature dependence

Stress strain graph of thermoplastic material.

Thermoplastics are elastic and flexible above a glass transition temperature Tg, specific for each one — the midpoint of a temperature range in contrast to the sharp melting point and freezing point of a pure crystalline substance like water. Below a second, higher melting temperature, Tm, also the midpoint of a range, most thermoplastics have crystalline regions alternating with amorphous regions in which the chains approximate random coils. The amorphous regions contribute elasticity and the crystalline regions contribute strength and rigidity, as is also the case for non-thermoplastic fibrous proteins such as silk. (Elasticity does not mean they are particularly stretchy; e.g., nylon rope and fishing line.) Above Tm all crystalline structure disappears and the chains become randomly inter dispersed. As the temperature increases above Tm, viscosity gradually decreases without any distinct phase change.

Thermoplastics can go through melting/freezing cycles repeatedly and the fact that they can be reshaped upon reheating gives them their name. This quality makes thermoplastics recyclable. The processes required for recycling vary with the thermoplastic. The plastics used for pop bottles are a common example of thermoplastics that can be and are widely recycled. Animal horn, made of the protein α-keratin, softens on heating, is somewhat reshapable, and may be regarded as a natural, quasi-thermoplastic material.

Some thermoplastics normally do not crystallize: they are termed "amorphous" plastics and are useful at temperatures below the Tg. They are frequently used in applications where clarity is important. Some typical examples of amorphous thermoplastics are PMMA, PS and PC. Generally, amorphous thermoplastics are less chemically resistant and can be subject to stress cracking. Thermoplastics will crystallize to a certain extent and are called "semi-crystalline" for this reason. Typical semi-crystalline thermoplastics are PE, PP, PBT and PET. The speed and extent to which crystallization can occur depends in part on the flexibility of the polymer chain. Semi-crystalline thermoplastics are more resistant to solvents and other chemicals. If the crystallites are larger than the wavelength of light, the thermoplastic is hazy or opaque. Semi-crystalline thermoplastics become less brittle above Tg. If a plastic with otherwise desirable properties has too high a Tg, it can often be lowered by adding a low-molecular-weight plasticizer to the melt before forming (Plastics extrusion; molding) and cooling. A similar result can sometimes be achieved by adding non-reactive side chains to the monomers before polymerization. Both methods make the polymer chains stand off a bit from one another. Before the introduction of plasticizers, plastic automobile parts often cracked in cold winter weather. Another method of lowering Tg (or raising Tm) is to incorporate the original plastic into a copolymer, as with graft copolymers of polystyrene, or into a composite material. Lowering Tg is not the only way to reduce brittleness. Drawing (and similar processes that stretch or orient the molecules) or increasing the length of the polymer chains also decrease brittleness.

Although modestly vulcanized natural and synthetic rubbers are stretchy, they are elastomeric thermosets, not thermoplastics. Each has its own Tg, and will crack and shatter when cold enough so that the crosslinked polymer chains can no longer move relative to one another. But they have no Tm and will decompose at high temperatures rather than melt. Recently, thermoplastic elastomers have become available!

Terminology

The literature on thermoplastics is huge, and can be quite confusing, as the same chemical can be available in many different forms (for example, at different molecular weights), which might have quite different physical properties. The same chemical can be referred to by many different tradenames, by different abbreviations; two chemical compounds can share the same name; a good example of the latter is the word "Teflon" which is used to refer to a specific polymer (PTFE); to related polymers such as PFA, and generically to fluoropolymers.

Furthermore, over the last 30 years, there has been tremendous change in the plastics industry, with many companies going out of business or merging into other companies. Many production plants frequently changed hands or have been relocated to emerging countries in Eastern Europe or Asia, with different trademarks.

Testing

Testing of thermoplastics can take various forms.

Tensile tests — ISO 527 -1/-2 and ASTM D 638 set out the standardized test methods. These standards are technically equivalent. However they are not fully comparable because of the difference in testing speeds. The modulus determination requires a high accuracy of ± 1 micrometer for the dilatometer.

Flexural tests — 3-points flexural tests are among the most common and classic methods for semi rigid and rigid plastics.

Pendulum impact tests — impact tests are used to measure the behavior of materials at higher deformation speeds. Pendulum impact testers are used to determine the energy required to break a standardized specimen by measuring the height to which the pendulum hammer rises after impacting the test piece.

List of thermoplastics

See also

References