Polyvinylidene fluoride

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Polyvinylidene fluoride
Polyvinylidenfluorid.svg
Names
IUPAC name
Poly(1,1-difluoroethylene) [1]
Other names
Polyvinylidene difluoride; poly(vinylene fluoride); Kynar; Hylar; Solef; Sygef; poly(1,1-difluoroethane)
Identifiers
ChEBI
ChemSpider
  • None
ECHA InfoCard 100.133.181 OOjs UI icon edit-ltr-progressive.svg
MeSH polyvinylidene+fluoride
PubChem CID
Properties
−(C2H2F2)n−
AppearanceWhitish or translucent solid
Melting point 177 °C (351 °F)
Insoluble
Structure
2.1 D [2]
Related compounds
Related compounds
 PVF, PVC, PTFE
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Polyvinylidene fluoride or polyvinylidene difluoride (PVDF) is a highly non-reactive thermoplastic fluoropolymer produced by the polymerization of vinylidene difluoride. Its chemical formula is (C2H2F2)n.

PVDF is a specialty plastic used in applications requiring the highest purity, as well as resistance to solvents, acids and hydrocarbons. PVDF has low density 1.78 g/cm3 in comparison to other fluoropolymers, like polytetrafluoroethylene.

It is available in the form of piping products, sheet, tubing, films, plate and an insulator for premium wire. It can be injected, molded or welded and is commonly used in the chemical, semiconductor, medical and defense industries, as well as in lithium-ion batteries. It is also available as a cross-linked closed-cell foam, used increasingly in aviation and aerospace applications, and as an exotic 3D printer filament. It can also be used in repeated contact with food products, as it is FDA-compliant and non-toxic below its degradation temperature. [3]

As a fine powder grade, it is an ingredient in high-end paints for metals. These PVDF paints have extremely good gloss and color retention. They are in use on many prominent buildings around the world, such as the Petronas Towers in Malaysia and Taipei 101 in Taiwan, as well as on commercial and residential metal roofing.

PVDF membranes are used in western blots for the immobilization of proteins, due to its non-specific affinity for amino acids.

PVDF is also used as a binder component for the carbon electrode in supercapacitors and for other electrochemical applications.

Names

PVDF is sold under a variety of brand names including KF (Kureha), Hylar (Solvay), Kynar (Arkema) and Solef (Solvay).

Synthesis

The easiest way of synthesizing PVDF is the radical polymerization of vinylidene fluoride (VF2), however, the polymerization is not completely regiospecific. The asymmetric structure of VF2 leads to the orientation isomers during the polymerization. The configuration of the monomer in the chain can be either "head to head" or "head to tail".

Figure 4: Three orientation isomers of polyvinylidene fluoride Ferroelectric-wiki-w1.png
Figure 4: Three orientation isomers of polyvinylidene fluoride

To get more control on the regiospecific polymer synthesis, copolymerization was proposed. One of these methods is introducing the precursor polymer made from copolymerization of VF2 with either 1-chloro-2,2-difluoroethylene (CVF2) or 1-bromo-2,2-difluoroethylene( BVF2). The chlorinated or brominated monomers are attacked at their CF2 carbon by growing –CH2CF2∙ radical. After reductive dechlorination or debromination with tri-n-butyltin hydride they become a reversed VF2 unit in the final polymer. Therefore, a regioisomer of PVDF is formed. [4]

Figure 5: Scheme of regiospecific polymer synthesis Ferroelectric-wiki-w2.png
Figure 5: Scheme of regiospecific polymer synthesis
Figure 6: Schematic description of two most common conformations of PVDF, the left one is tg tg and the right one is all trans, the yellow sphere represents fluorine atom, the white sphere represents hydrogen atom and the grey sphere represents the carbon atom. Ferroelectric-wiki-w3.png
Figure 6: Schematic description of two most common conformations of PVDF, the left one is tg tg and the right one is all trans, the yellow sphere represents fluorine atom, the white sphere represents hydrogen atom and the grey sphere represents the carbon atom.

Properties

In 1969, strong piezoelectricity was observed in PVDF, with the piezoelectric coefficient of poled (placed under a strong electric field to induce a net dipole moment) thin films as large as 6–7 pC/N: 10 times larger than that observed in any other polymer. [5]

PVDF has a glass transition temperature (Tg) of about −35 °C and is typically 50–60% crystalline. To give the material its piezoelectric properties, it is mechanically stretched to orient the molecular chains and then poled under tension. PVDF exists in several phases depending on the chain conformations as trans (T) or gauche (G) linkages: TGTG' for α and δ phase, TTTT for β phases, and TTTGTTTG' for γ and ε phases. The α and ε conformations lack piezoelectric properties because of the antiparallel alignment of dipoles within its unit cell. The β, γ, and δ phases feature a parallel arrangement of dipoles, rendering them polar crystals with a non-zero dipole moment. Among these phases, the β phase stands out due to its remarkable remnant polarization and the highest dipolar moment per unit cell, garnering more interest compared to the others. [6] When poled, PVDF is a ferroelectric polymer, exhibiting efficient piezoelectric and pyroelectric properties. [7] These characteristics make it useful in sensor and battery applications. Thin films of PVDF are used in some newer thermal camera sensors.

Unlike other popular piezoelectric materials, such as lead zirconate titanate (PZT), PVDF has a negative d33 value. Physically, this means that PVDF will compress instead of expand or vice versa when exposed to the same electric field. [8]

Thermal

PVDF resin has been subjected to high-heat experiments to test its thermal stability. PVDF was held for 10 years at 302 °F (150 °C), and following measurements indicated no thermal or oxidative breakdown occurred [ citation needed ]. PVDF resin has been recorded stable up to 707 °F (375 °C). [9]

Chemical compatibility

PVDF exhibits an increased chemical resistance and compatibility among thermoplastic materials. PVDF is considered to have excellent / inert resistance to:[ citation needed ]

Chemical sensitivity

PVDF, similar to other fluoropolymers, exhibits chemical sensitivity, in general, with the following chemical families:

Intrinsic properties and resistance

Polyvinylidene fluoride expresses inherent resistance characteristics in certain high-focus applications. Namely these are: ozone oxidation reactions, nuclear radiation, UV damage, and microbiological, fungus growth.[ citation needed ] PVDF's resistance to these conditions is fairly distinctive among thermoplastic materials. PVDF's carbon and fluoride elemental stability contributes to this resistance, as well as the polymeric integration of PVDF during its processing.[ citation needed ]

Processing

PVDF may be synthesized from the gaseous vinylidene fluoride (VDF) monomer by a free-radical (or controlled-radical) polymerization process. This may be followed by processes such as melt casting, or processing from a solution (e.g. solution casting, spin coating, and film casting). Langmuir–Blodgett films have also been made. In the case of solution-based processing, typical solvents used include dimethylformamide and the more volatile butanone. In aqueous emulsion polymerization, the fluorosurfactant perfluorononanoic acid is used in anion form as a processing aid by solubilizing monomers. [11] Compared to other fluoropolymers, it has an easier melt process because of its relatively low melting point of around 177 °C.

Processed materials are typically in the non-piezoelectric alpha phase. The material must either be stretched or annealed to obtain the piezoelectric beta phase. The exception to this is for PVDF thin films (thickness in the order of micrometres). Residual stresses between thin films and the substrates on which they are processed are great enough to cause the beta phase to form.

In order to obtain a piezoelectric response, the material must first be poled in a large electric field. Poling of the material typically requires an external field of above 30 megavolts per metre (MV/m). Thick films (typically >100  μm) must be heated during the poling process in order to achieve a large piezoelectric response. Thick films are usually heated to 70–100 °C during the poling process.

A quantitative defluorination process was described by mechanochemistry, [12] for safe eco-friendly PVDF waste processing.

Applications

PVDF piping used to carry ultrapure water A UPW Installation using PVDF Piping.png
PVDF piping used to carry ultrapure water

PVDF is a thermoplastic that expresses versatility for applications similar to other thermoplastics, particularly fluoropolymers. PVDF resin is heated and handled for use in extrusion and injection molding to produce PVDF pipes, sheets, coatings, films, and molded PVDF products, such as bulk containers. Common industry applications for PVDF thermoplastics include: [10]

In electronics / electricity

PVDF is commonly used as insulation on electrical wires, because of its combination of flexibility, low weight, low thermal conductivity, high chemical corrosion resistance, and heat resistance. Most of the narrow 30-gauge wire used in wire wrap circuit assembly and printed circuit board rework is PVDF-insulated. In this use the wire is generally referred to as "Kynar wire", from the trade name.

The piezoelectric properties of PVDF are exploited in the manufacture of tactile sensor arrays, inexpensive strain gauges, and lightweight audio transducers. Piezoelectric panels made of PVDF are used on the Venetia Burney Student Dust Counter, a scientific instrument of the New Horizons space probe that measures dust density in the outer Solar System. [13]

PVDF is the standard binder material used in the production of composite electrodes for lithium-ion batteries. [14] Solution of PVDF 1−2% by mass in N-methyl-2-pyrrolidone (NMP) is mixed with an active lithium storage material such as graphite, silicon, tin, LiCoO2, LiMn2O4, or LiFePO4 and a conductive additive such as carbon black or carbon nanofibers. This slurry is cast onto a metallic current collector, and the NMP is evaporated to form a composite or paste electrode. PVDF is used because it is chemically inert over the potential range used and does not react with the electrolyte or lithium.

In biomedical science

In the biomedical sciences, PVDF is used in immunoblotting as an artificial membrane (usually with 0.22 or 0.45-micrometre pore sizes), on which proteins are transferred using electricity (see western blotting). PVDF is resistant to solvents and, therefore, these membranes can be easily stripped and reused to look at other proteins. PVDF membranes may be used in other biomedical applications as part of a membrane filtration device, often in the form of a syringe filter or wheel filter. The various properties of this material, such as heat resistance, resistance to chemical corrosion, and low protein binding properties, make this material valuable in the biomedical sciences for preparation of medications as a sterilizing filter, and as a filter to prepare samples for analytical techniques such as high-performance liquid chromatography (HPLC), where small amounts of particulate matter can damage sensitive and expensive equipment.

PVDF transducers have the advantage of being dynamically more suitable for modal testing than semiconductor piezoresistive transducers and more compliant for structural integration than piezoceramic transducers. For those reasons, the use of PVDF active sensors is a keystone for the development of future structural-health monitoring methods, due to their low cost and compliance. [15]

In high-temperature processes

PVDF is used as piping, sheet, and internal coatings in high-temperature, hot acid, radiation environment applications due to PVDF's resistance characteristics and upper temperature thresholds. As piping, PVDF is rated up to 248 °F (120 °C). Examples of PVDF uses include nuclear reactor waste handling, chemical synthesis and production, (sulfuric acid, common), air plenums, and boiler service pipe.

Other uses

PVDF is used for specialty monofilament fishing lines, sold as fluorocarbon replacements for nylon monofilament. The surface is harder, so it is more resistant to abrasion and sharp fish teeth. Its refractive index is lower than nylon, which makes the line less discernible to sharp fish eyes. It is also denser than nylon, making it sink faster towards fish. [16]

Other forms

Copolymers

The copolymer Poly(vinylidene fluoride-co-hexafluoropropylene) or PVDF-HFP is used as a co-polymer in the blades of artificial turf. [17]

Copolymers of PVDF are also used in piezoelectric and electrostrictive applications. One of the most commonly used copolymers is P(VDF-trifluoroethylene), usually available in ratios of about 50:50 and 65:35 by mass (equivalent to about 56:44 and 70:30 molar fractions). Another one is P(VDF-tetrafluoroethylene). They improve the piezoelectric response by improving the crystallinity of the material.

While the copolymers' unit structures are less polar than that of pure PVDF, the copolymers typically have a much higher crystallinity. This results in a larger piezoelectric response: d33 values for P(VDF-TFE) have been recorded to be as high as −38 p C/N [18] compared to −33 pC/N in pure PVDF. [19]

Terpolymers

Terpolymers of PVDF are the most promising one in terms of electromechanically induced strain. The most commonly used PVDF-based terpolymers are P(VDF-TrFE-CTFE) and P(VDF-TrFE-CFE). [20] [21] This relaxor-based ferroelectric terpolymer is produced by random incorporation of the bulky third monomer (chlorotrifluoroethylene, CTFE) into the polymer chain of P(VDF-TrFE) copolymer (which is ferroelectric in nature). This random incorporation of CTFE in P(VDF-TrFE) copolymer disrupts the long-range ordering of the ferroelectric polar phase, resulting in the formation of nano-polar domains. When an electric field is applied, the disordered nano-polar domains change their conformation to all-trans conformation, which leads to large electrostrictive strain and a high room-temperature dielectric constant of ~50. [22]

See also

Related Research Articles

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<span class="mw-page-title-main">Thermoplastic</span> Plastic that softens with heat and hardens on cooling

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References

  1. ↑ "poly(vinylene fluoride) (CHEBI:53250)" . Retrieved 14 July 2012.
  2. ↑ Zhang, Q. M., Bharti, V., Kavarnos, G., Schwartz, M. (Ed.), (2002). "Poly (Vinylidene Fluoride) (PVDF) and its Copolymers", Encyclopedia of Smart Materials, Volumes 1–2, John Wiley & Sons, 807–825.
  3. ↑ "PVDF (Polyvinylidene fluoride, Tecaflon ®, Solef®, Kynar®) | Plastics International".
  4. ↑ Cais, R.E.; Kometani, J.M. (1985). "Synthesis and two-dimensional NMR of highly aregic poly(vinylidene fluoride)". Macromolecules. 18 (6): 1354–1357. Bibcode:1985MaMol..18.1354C. doi:10.1021/ma00148a057.
  5. ↑ Kawai, Heiji (1969). "The Piezoelectricity of Poly (vinylidene Fluoride)". Japanese Journal of Applied Physics. 8 (7): 975–976. Bibcode:1969JaJAP...8..975K. doi:10.1143/JJAP.8.975. S2CID   122316276.
  6. ↑ Martins, P.; Lopes, A.C.; Lanceros-Mendez, S. (April 2014). "Electroactive phases of poly(vinylidene fluoride): Determination, processing and applications". Progress in Polymer Science. 39 (4): 683–706. doi:10.1016/j.progpolymsci.2013.07.006. ISSN   0079-6700.
  7. ↑ Lolla, Dinesh; Gorse, Joseph; Kisielowski, Christian; Miao, Jiayuan; Taylor, Philip L.; Chase, George G.; Reneker, Darrell H. (17 December 2015). "Polyvinylidene fluoride molecules in nanofibers, imaged at atomic scale by aberration corrected electron microscopy". Nanoscale. 8 (1): 120–128. Bibcode:2015Nanos...8..120L. doi:10.1039/c5nr01619c. ISSN   2040-3372. PMID   26369731. S2CID   205976678.
  8. ↑ Lolla, Dinesh; Lolla, Manideep; Abutaleb, Ahmed; Shin, Hyeon U.; Reneker, Darrell H.; Chase, George G. (9 August 2016). "Fabrication, Polarization of Electrospun Polyvinylidene Fluoride Electret Fibers and Effect on Capturing Nanoscale Solid Aerosols". Materials. 9 (8): 671. Bibcode:2016Mate....9..671L. doi: 10.3390/ma9080671 . PMC   5510728 . PMID   28773798.
  9. ↑ "Physical and Mechanical Properties". Arkema, Inc. Innovative Chemistry.
  10. 1 2 "PVDF Performance & Characteristics Data" (PDF). Plastic Pipe Solutions.
  11. ↑ Prevedouros K.; Cousins I. T.; Buck R. C.; Korzeniowski S. H. (January 2006). "Sources, fate and transport of perfluorocarboxylates". Environ. Sci. Technol. 40 (1): 32–44. Bibcode:2006EnST...40...32P. doi:10.1021/es0512475. PMID   16433330.
  12. ↑ Zhang, Qiwu; Lu, Jinfeng; Saito, Fumio; Baron, Michel (2001). "Mechanochemical solid-phase reaction between polyvinylidene fluoride and sodium hydroxide" (PDF). Journal of Applied Polymer Science. 81 (9): 2249. doi:10.1002/app.1663.
  13. ↑ Horanyi, Mihaly (2010). "First results from the Venetia Burney Student Dust Counter on the New Horizons mission". Geophysical Research Letters. 37 (11). doi: 10.1029/2010GL043300 . S2CID   129795884 . Retrieved 17 August 2023.
  14. ↑ Ordoñez, J.; Gago, E. J.; Girard, A. (1 July 2016). "Processes and technologies for the recycling and recovery of spent lithium-ion batteries" (PDF). Renewable and Sustainable Energy Reviews. 60: 195–205. doi:10.1016/j.rser.2015.12.363. ISSN   1364-0321.
  15. ↑ Guzman, E.; Cugnoni, J.; Gmür, T. (2013). "Survivability of integrated PVDF film sensors to accelerated ageing conditions in aeronautical/aerospace structures". Smart Mater. Struct. 22 (6): 065020. Bibcode:2013SMaS...22f5020G. doi:10.1088/0964-1726/22/6/065020. S2CID   136758382.
  16. ↑ Seaguar history  — Kureha America, Inc. manufacturer's site. Archived 20 June 2010 at the Wayback Machine
  17. ↑ McMenemy, Jeff (10 December 2021). "Portsmouth to test for PFAS in new turf field. Is it dangerous? City says no. Others disagree". Portsmouth Herald. Retrieved 30 December 2021.
  18. ↑ Omote, Kenji; Ohigashi, Hiroji; Koga, Keiko (1997). "Temperature dependence of elastic, dielectric, and piezoelectric properties of "single crystalline" films of vinylidene fluoride trifluoroethylene copolymer". Journal of Applied Physics. 81 (6): 2760. Bibcode:1997JAP....81.2760O. doi:10.1063/1.364300.
  19. ↑ Nix, E. L.; Ward, I. M. (1986). "The measurement of the shear piezoelectric coefficients of polyvinylidene fluoride". Ferroelectrics. 67 (1): 137–141. Bibcode:1986Fer....67..137N. doi:10.1080/00150198608245016.
  20. ↑ Xu, Haisheng; Cheng, Z.-Y.; Olson, Dana; Mai, T.; Zhang, Q. M.; Kavarnos, G. (16 April 2001). "Ferroelectric and electromechanical properties of poly(vinylidene-fluoride–trifluoroethylene–chlorotrifluoroethylene) terpolymer". Applied Physics Letters. 78 (16). AIP Publishing LLC, American Institute of Physics: 2360–2362. Bibcode:2001ApPhL..78.2360X. doi:10.1063/1.1358847.
  21. ↑ Bao, Hui-Min; Song, Jiao-Fan; Zhang, Juan; Shen, Qun-Dong; Yang, Chang-Zheng; Zhang, Q. M. (3 April 2007). "Phase Transitions and Ferroelectric Relaxor Behavior in P(VDF−TrFE−CFE) Terpolymers". Macromolecules. 40 (7). ACS Publications: 2371–2379. Bibcode:2007MaMol..40.2371B. doi:10.1021/ma062800l.
  22. ↑ Ahmed, Saad; Arrojado, Erika; Sigamani, Nirmal; Ounaies, Zoubeida (14 May 2015). "Electric field responsive origami structures using electrostriction-based active materials". In Goulbourne, Nakhiah C. (ed.). Behavior and Mechanics of Multifunctional Materials and Composites 2015. Vol. 9432. Society of Photographic Instrumentation Engineers (SPIE). p. 943206. Bibcode:2015SPIE.9432E..06A. doi:10.1117/12.2084785. ISBN   978-1-62841-535-3. S2CID   120322803.
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