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Polyacrylonitrile

From Wikipedia, the free encyclopedia
Polyacrylonitrile
Names
IUPAC name
poly(1-acrylonitrile)
Other names
Polyvinyl cyanide[1]
Creslan 61
Properties
(C3H3N)n
Molar mass 53.0626 ± 0.0028 g/mol
C 67.91%, H 5.7%, N 26.4%
Appearance White solid
Density 1.184 g/cm3
Melting point 300 °C (572 °F; 573 K)
Boiling point Degrades
Insoluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Polyacrylonitrile (PAN) is a synthetic, semicrystalline organic polymer resin, with the linear formula (CH2CHCN)n.[2] Almost all PAN resins are copolymers with acrylonitrile as the main monomer. PAN is used to produce large variety of products including ultra filtration membranes, hollow fibers for reverse osmosis, fibers for textiles, and oxidized PAN fibers. PAN fibers are the chemical precursor of very high-quality carbon fiber. PAN is first thermally oxidized in air at 230 °C to form an oxidized PAN fiber and then carbonized above 1000 °C in inert atmosphere to make carbon fibers found in a variety of both high-tech and common daily applications such as civil and military aircraft primary and secondary structures, missiles, solid propellant rocket motors, pressure vessels, fishing rods, tennis rackets and bicycle frames. It is a component repeat unit in several important copolymers, such as styrene-acrylonitrile (SAN) and acrylonitrile butadiene styrene (ABS) plastic.

History

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Polyacrylonitrile (PAN) was first synthesized in 1930 by Hans Fikentscher and Claus Heuck in the Ludwigshafen works of the German chemical conglomerate IG Farben.[3] However, as PAN is non-fusible, and did not dissolve in any of the industrial solvents being used at the time, further research into the material was halted.[4] In 1931, Herbert Rein, head of polymer fiber chemistry at the Bitterfeld plant of IG Farben, obtained a sample of PAN while visiting the Ludwigshafen works.[5] He found that pyridinium benzylchloride, an ionic liquid, would dissolve PAN.[6] He spun the first fibers based on PAN in 1938, using aqueous solutions of quaternary ammonium sodium thiocyanate and aluminum perchlorate for the production process and considered other solvents including DMF. However, commercial introduction was delayed due to the wartime stresses on infrastructure, inability to melt the polymer without degradation, and solvents to allow solution processing were not known yet.[7][8] The first mass production run of PAN fiber was in 1946 by American chemical conglomerate DuPont. The German intellectual property had been stolen in Operation Paperclip. The product, branded as Orlon, was based on a patent filed exactly seven days after a nearly identical German claim.[9] [failed verification] In the German Democratic Republic (GDR), industrial polyacrylonitrile fibre production was started in 1956 at the VEB Film- und Chemiefaserwerk Agfa Wolfen due to the preliminary work of the "Wolcrylon" collective (de:Max Duch, Herbert Lehnert et al.). Prior to this, the preconditions for the production of the raw materials had been created at the Buna Werke Schkopau (Polyacrylonitrile) and Leuna works (Dimethylformamide).[10] In the same year, the collective was awarded the GDR's National Prize II Class for Science and Technology for its achievements.[11]

Physical properties

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Although it is thermoplastic, polyacrylonitrile does not melt under normal conditions. It degrades before melting. It melts above 300 °C if the heating rates are 50 degrees per minute or above.[12]

Glass transition temperature is around 95 °C and fusion temperature is at 322 °C. PAN is soluble in polar solvents, such as dimethylformamide, dimethylacetamide, ethylene and propylene carbonates, and in aqueous solutions of sodium thiocyanate, zinc chloride or nitric acid.[13] Solubility parameters: 26.09 MPa1/2 (25 °C) are 25.6 to 31.5 J1/2 cm−3/2. Dielectric constants: 5.5 (1 kHz, 25 °C), 4.2 (1 MHz, 25 °C).Can behave as branched as well as linear polymer.

Synthesis

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Most commercial methods for the synthesis of PAN are based on free radical polymerization of acrylonitrile.[14] In most of the cases, 10% amounts of other vinyl comonomers are also used (1–10%) along with AN depending on the final application. Comonomers include acrylic acid, acrylamide, allyl compounds, and sulfonated styrene.[2] Anionic polymerization also can be used for synthesizing PAN. For textile applications, molecular weight in the range of 40,000 to 70,000 is used.[citation needed] For producing carbon fiber higher molecular weight is desired.[15]

In the production of carbon fibers containing 600 tex (6k) PAN tow, the linear density of filaments is 0.12 tex and the filament diameter is 11.6 μm which produces a carbon fiber that has the filament strength of 417 kgf/mm2 and binder content of 38.6%. This data is demonstrated in the Indexes for Experimental Batches of PAN Precursor and Carbon Fibers Made from It table.[16]

Applications

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Homopolymers of polyacrylonitrile have been used as fibers in hot gas filtration systems, outdoor awnings, sails for yachts, and fiber-reinforced concrete. Copolymers containing polyacrylonitrile are often used as fibers to make knitted clothing like socks and sweaters, as well as outdoor products like tents and similar items. If the label of a piece of clothing says "acrylic", then it is made out of some copolymer of polyacrylonitrile. It was made into the spun fiber at DuPont in 1942 and marketed under the name of Orlon. Acrylonitrile is commonly employed as a comonomer with styrene, e.g. acrylonitrile, styrene and acrylate plastics. Labelling of items of clothing with acrylic (see acrylic fiber) means the polymer consists of at least 85% acrylonitrile as the monomer. A typical comonomer is vinyl acetate, which can be solution-spun readily to obtain fibers that soften enough to allow penetration by dyes. The advantages of the use of these acrylics are that they are low-cost compared to natural fiber, they offer better sunlight resistance and have superior resistance to attack by moths. Acrylics modified with halogen-containing comonomers are classified as modacrylics, which by definition contain more than PAN percentages between 35-85%. Incorporation of halogen groups increases the flame resistance of the fiber, which makes modacrylics suitable for the use in sleepwear, tents and blankets. Some mattresses also use them to meet the flame resistance requirements in North America.[17] However, the disadvantage of these products is that they are costly and can shrink after drying.

PAN absorbs many metal ions and aids the application of absorption materials. Polymers containing amidoxime groups can be used for the treatment of metals because of the polymers’ complex-forming capabilities with metal ions.[18]

PAN has properties involving low density, thermal stability, high strength and modulus of elasticity. These unique properties have made PAN an essential polymer in high tech.

Its high tensile strength and tensile modulus are established by fiber sizing, coatings, production processes, and PAN's fiber chemistry. Its mechanical properties derived are important in composite structures for military and commercial aircraft.[19]

Carbon fiber

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Polyacrylonitrile is used as the precursor for 90% of carbon fiber production.[20] Approximately 20–25% of Boeing and Airbus wide-body airframes are carbon fibers. However, applications are limited by PAN's high price of around $15/lb.[21]

Glassy carbon

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Glassy carbon, a common electrode material in electrochemistry, is created by heat-treating blocks of polyacrylonitrile under pressure at 1000 to 3000 °C over a period of several days. The process removes non-carbon atoms and creates a conjugated double bond structure with excellent conductivity.[22]

Support polymer

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Divinylbenzene-crosslinked polyacrylonitrile is a precursor to ion exchange resins. Hydrolysis converts the nitrile groups to carboxylic acids. Amberlite IRC86 is one commercial product. These weakly acidic resins have high affinities for divalent metal ions like Ca2+ and Mg2+.[23]

References

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  1. ^ J Gordon Cook (1984). Handbook of Textile Fibres: Man-Made Fibres. Woodhead Publishing. p. 393. ISBN 9781855734852.
  2. ^ a b Nogaj, Alfred; Süling, Carlhans; Schweizer, Michael (2011). "Fibers, 8. Polyacrylonitrile Fibers". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.o10_o04. ISBN 978-3527306732.
  3. ^ H. Finkentscher, C. Heuck, DE Patent 654989, Verfahren zur Herstellung von Polymerisationprodukten, Anmeldetag 18.2.1930 [1]
  4. ^ Walter Wetzel, Entdeckungsgeschichte der Polyfluorethylene - Zufall oder Ergebnis gezielter Forschung? N.T. M. 13 (2005) 79–91
  5. ^ "KUNSTFASERN / INDUSTRIE : Das Salz der Mode - DER SPIEGEL 20/1955". www.spiegel.de.
  6. ^ H. Rein, DE-Patent 631756, Verfahren zur Lösung von polymerem Acrylsäurenitril, Anmeldetag 8 August 1934 [2]
  7. ^ Rein, Herbert (1948). "Polyacrylnitril-Fasern Eine neue Gruppe von synthethischen Fasern". Angewandte Chemie. 60 (6): 159–161. Bibcode:1948AngCh..60..159R. doi:10.1002/ange.19480600607.
  8. ^ Bunsell, A.R. (18 January 2018). Handbook of properties of textile and technical fibres (2nd ed.). Woodhead Publishing. ISBN 9780081012727.
  9. ^ C. H. Ray US Patent 2 404 713, Method for Preparing Polymeric Solutions, Filing date: 17.06.1942 [3]
  10. ^ Herbert Bode Geschichte der Chemiefaser-industrie der Deutschen Demokratischen Republik. In: Mitteilungen, Gesellschaft Deutscher Chemiker / Fachgruppe Geschichte der Chemie (Frankfurt/Main), Bd. 14 (1998), S. 162. Retrieves 13 December 2021.
  11. ^ Lothar Rudolph: Eigenschaften, Verspinnung und Einsatzmöglichkeiten von Wolcrylon. Mitteilung aus dem Zellwolle-Technikum der VEB Filmfabrik Agfa Wolfen. Wolfen 1954.
  12. ^ Gupta, A. K.; Paliwal, D. K.; Bajaj, P. (1998). "Melting behavior of acrylonitrile polymers". Journal of Applied Polymer Science. 70 (13): 2703–2709. doi:10.1002/(sici)1097-4628(19981226)70:13<2703::aid-app15>3.3.co;2-u.
  13. ^ Internet, D4W Comunicação - Soluções em. "IGTPAN". www.igtpan.com. Retrieved 2018-05-10.{{cite web}}: CS1 maint: numeric names: authors list (link)
  14. ^ Guyot, Alain (1986). "16 - Precipitation Polymerization". Comprehensive Polymer Science and Supplements. Vol. 4. Pergamon. p. 261-273. doi:10.1016/B978-0-08-096701-1.00131-2. ISBN 978-0-08-096701-1.
  15. ^ Kaur, Jasjeet; Millington, Keith; Smith, Shaun (2016-10-10). "Producing high-quality precursor polymer and fibers to achieve theoretical strength in carbon fibers: A review: REVIEW". Journal of Applied Polymer Science. 133 (38). doi:10.1002/app.43963. hdl:10536/DRO/DU:30102165.
  16. ^ Serkov, A; Radishevskii, M (2008). "Status and Prospects For Production Of Carbon Fibres Based on Polyacrylonitrile". Fibre Chemistry. 40 (1): 24–31. doi:10.1007/s10692-008-9012-y. S2CID 137117495.
  17. ^ Szostech, Michael. "Fiberglass in Mattresses". Retrieved 11 August 2023.
  18. ^ Delong, Liu (2011). "Synthesis of Polyacrylonitrile by Single-electron Transfer-living Radical Polymerization Using Fe(0) as Catalyst and Its Absorption Properties After Modification". Journal of Polymer Science Part A: Polymer Chemistry. 49 (13): 2916–2923. Bibcode:2011JPoSA..49.2916L. doi:10.1002/pola.24727.
  19. ^ "Polyacrylonitrile (PAN) Carbon Fibers Industrial Capability Assessment" (PDF). United States of America Department of Defense. Archived from the original (PDF) on 4 March 2016. Retrieved 4 December 2013.
  20. ^ "Top 9 Things You Didn't Know about Carbon Fiber | Department of Energy". Energy.gov. 2013-03-29. Retrieved 2013-12-08.
  21. ^ John McElroy. "Manufacturing advances bring carbon fiber closer to mass production". Autoblog. Retrieved 2013-12-08.
  22. ^ Handbook of Electrochemistry. Elsevier. 2021-07-02.
  23. ^ De Dardel, François; Arden, Thomas V. (2008). "Ion Exchangers". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a14_393.pub2. ISBN 978-3527306732.
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