- Polyvinylidene fluoride
Name = Polyvinylidene fluoride
ImageFile = PVDF.png
IUPACName = poly-1,1-difluoroethene
OtherNames = polyvinylidene difluoride
Name = References
Section1 = Chembox Identifiers
CASNo = 24937-79-9
Section2 = Chembox Properties
Formula = -(CH2CF2)n-
Appearance = whitish or translucent solid
Solubility = not soluble in water
Section3 = Chembox Structure
CrystalStruct = mm2(Kawai, 1969)
Dipole = 2.1 D(Zhang, 2002)
Section7 = Chembox Hazards
Section8 = Chembox Related
OtherCpds = PVC,
Polyvinylidene Fluoride, or PVDF is a highly non-reactive and pure
thermoplastic fluoropolymer. It is also known as KYNAR, HYLAR or SYGEF.
PVDF is a specialty plastic material in the fluoropolymer family; it is used generally in applications requiring the highest purity, strength, and resistance to solvents, acids, bases and heat and low smoke generation during a fire event. Compared to other fluoropolymers, it has an easier melt process because of its relatively low melting point.
It has a relatively low density (1.78) and low cost compared to the other fluoropolymers. It is available as 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.
A fine powder grade, KYNAR 500 PVDF or HYLAR 5000 PVDF, is also used as the principal ingredient of high-end paints for metals. These PVDF paints have extremely good gloss and color retention, and they are in use on many prominent buildings around the world, e.g. the Petronas Towers in Malaysia and Taipei 101 in Taiwan, as well as on commercial and residential metal roofing. PPG Industries, Inc. is a well-known supplier of such PVDF-containing coatings.
PVDF membranes are used for
western blots for immobilization of proteins, due to its non-specific affinity for amino acids.
In 1969, the strong
piezoelectricityof PVDF was observed by Kawai "et al." The piezoelectric coefficient of poled thin films of the material werereported to be as large as 6-7 pCN-1: 10 times larger than that observed in any other polymer.
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 forms: alpha (TGTG'), beta (TTTT), and gamma (TTTGTTTG') phases, depending on the chain conformations as trans (T) or gauche (G) linkages. When poled, PVDF is a ferroelectricpolymer, exhibiting efficient piezoelectricand pyroelectricproperties. These characteristics make it useful in sensorand battery applications. Thin films of PVDF are used in some newer thermal camerasensors.
Unlike other popular piezoelectric materials, such as
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.
PVDF may be synthesized from the gaseous
VDFmonomer via 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 (LB) films have also been made. In the case of solution-based processing, typical solvents used include DMF as well as the more volatile MEK. For characterization of the molecular weight via gel permeation chromatography(also called SEC), solvents such as DMSO or THF may be used.
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 >=30 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 (Zhang , 2001), for safe eco-friendly PVDF waste processing.
Copolymers of PVDF are also used in piezoelectric and electrostrictive applications. One of the most commonly-used copolymers is P(VDF-TrFE), usually available in ratios of about 50:50 wt% and 65:35 wt% (equivalent to about 56:44 mol% and 70:30 mol%). Another one is P(VDF-TFE). 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-TrFE) have been recorded to be as high as -38 pC/N7 versus -33 pC/N in pure PVDF5.
# Kawai, H., (1969). "Jpn. J. Appl. Phys", 8, p975.
# 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.
# Vinogradov, A., Schwartz, M. (Ed.), (2002). "Piezoelectricity in Polymers", "Encyclopedia of Smart Materials, Volumes 1-2", John Wiley & Sons, 780-792.
# Tasaka, S., Miyata, S., (1981). "Ferroelectrics", 32 (1), 17-23.
# E. L. Nix and I. M. Ward, (1986) Ferroelectrics 67, 137.
# K. Tashiro, M. Kobayashi, H. Tadokoro, and E. Fukada, (1980). Macromolecules 13, 691
# Kenji, O., Hiroji, O., Keiko, K., (1996). J. Appl. Phys. 81, 2760.
# Zhang, QW., Lu, J.F, Saito, F., Baron, M., (2001). J. Appl. Polym. Sci. 81 (9), 2249-2252.
* [http://peswiki.com/index.php?title=Power_Recovery_Systems Power Recovery Systems]
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