FKM is a family of fluorocarbon-based fluoroelastomer materials defined by ASTM International standard D1418 and ISO standard 1629. It is commonly called fluorine rubber or fluoro-rubber. FKM is an abbreviation of Fluorkautschukmaterial (i.e. fluorine rubber material). All FKMs contain vinylidene fluoride as the common monomer, to which different other monomers are added for specific types and functionalities, fitting the desired application. Originally developed by DuPont (under the brand name Viton, now owned by Chemours), FKMs are today also produced by many other companies, including Daikin (Dai-El), 3M (Dyneon), Solvay S.A. (Tecnoflon), HaloPolymer (Elaftor), Gujarat Fluorochemicals (Fluonox), and several Chinese manufacturers. Fluoroelastomers are more expensive than neoprene or nitrile rubber elastomers, and in comparison they provide additional resistance to heat and chemicals. There are three ways that the FKMs can be separated into classes: by their chemical composition, their fluorine content, or their cross-linking mechanism.
Types On the basis of their chemical composition FKMs can be divided into the following types:
Type-1 FKMs are composed of vinylidene fluoride (VDF) and hexafluoropropylene (HFP). Copolymers are the standard type of FKMs showing a good overall performance. Their fluorine content is approximately 66 weight percent. Type-2 FKMs are composed of VDF, HFP, and tetrafluoroethylene (TFE). Terpolymers have a higher fluorine content compared to copolymers (typically between 68 and 69 weight percent fluorine), which results in better chemical and heat resistance. Compression set and low temperature flexibility may be affected negatively. Type-3 FKMs are composed of VDF, TFE, and perfluoro(methyl vinyl ether) (PMVE). The addition of PMVE provides better low temperature flexibility compared to copolymers and terpolymers. Typically, the fluorine content of type-3 FKMs ranges from 62 to 68 weight percent. Type-4 FKMs are composed of propylene, TFE, and VDF. While base resistance is increased in type-4 FKMs, their swelling properties, especially in hydrocarbons, are worsened. Typically, they have a fluorine content of about 67 weight percent. Type-5 FKMs are composed of VDF, HFP, TFE, PMVE, and ethylene. Known for base resistance and high-temperature resistance to hydrogen sulfide.
Cross-linking mechanisms There are three established cross-linking mechanisms used in the curing process of FKMs.
Diamine cross-linking using a blocked diamine. In the presence of basic (alkaline) media, VDF is vulnerable to dehydrofluorination, which enables the addition of the diamine to the polymer chain. Typically, magnesium oxide is used to neutralize the resulting hydrofluoric acid and rearrange into magnesium fluoride and water. Although rarely used today, diamine curing provides superior rubber-to-metal bonding properties as compared with other cross-linking mechanisms. The diamine's capability to be hydrated makes the diamine cross-link vulnerable in aqueous media. Ionic cross-linking (dihydroxy cross-linking) was the next step in curing FKMs. This is today the most common cross-linking chemistry used for FKMs. It provides superior heat resistance, improved hydrolytic stability and better compression set than diamine curing. In contrast to diamine curing, the ionic mechanism is not an addition mechanism but an aromatic nucleophilic substitution. Dihydroxy aromatic compounds are used as the cross-linking agent, and quaternary phosphonium salts are typically used to accelerate the curing process. Peroxide cross-linking was originally developed for type 3 FKMs containing PMVE as diamine and bisphenolic cross-linking systems can lead to cleavage in a polymer backbone chain containing PMVE. While diamine and bisphenolic cross-linking are ionic reactions, peroxide cross-linking is a free-radical mechanism. Though peroxide cross-links are not as thermally stable as bisphenolic cross-links, they normally are the system of choice in aqueous media and nonaqueous electrolyte media.
Properties Fluoroelastomers provide excellent high temperature (up to 500 °F or 260 °C) and aggressive fluids resistance when compared with other elastomers, while combining the most effective stability to many sorts of chemicals and fluids such as oil, diesel, ethanol mix or body fluid. The performance of fluoroelastomers in aggressive chemicals depends on the nature of the base polymer and the compounding ingredients used for molding the final products (e.g. o-rings). Some formulations are generally compatible with hydrocarbons, but incompatible with ketones such as acetone and methyl ethyl ketone, ester solvents such as ethyl acetate, amines, and organic acids such as acetic acid. They can be easily distinguished from many other elastomers because of their high density of over 1800 kg/m3, significantly higher than most types of rubber.
Applications
Because of their outstanding performance they find use in a number of sectors, including the following:
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