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Teflon Fluorocarbon Resin


Table 1

*Typical values are unsuitable for specifications. Properties were measured at 23 degreesC (73 degreesF), unless otherwise noted.

**Statements regarding behavior in a flame situation are not intended to reflect hazards presented by this or any other material when under actual fire conditions. The following characteristics contribute to the unique properties of Teflon fluorocarbon resins:

Tefzel Fluoropolymer Resin
Replacement of fluorine in fluorocarbon polymers is only commercially successful when the fluorine is replaced by hydrogen or hydrogen and chlorine. However, the resulting polymers have significantly different properties from those of fully fluorinated resins. When this substitution occurs by regular alternation, polarity and mechanical properties are maximized. The polymer's polarity increases because the substituting elements:hydrogen and chlorine:have different electronegativities relative to fluorine. Also, the length of their bonds to carbon of the polymer backbone differ. Thus, the centers of electronegativity and electropositivity are not balanced between chains. The increased interpolymer chain attraction results in higher mechanical properties. In addition, the increased polarity/interpolymer attraction influences penetrants' permeation of the resin's amorphous component.

However, the presence of hydrogen or of hydrogen and chlorine sacrifices chemical and thermal stability. For example, in simple molecules, the C-H bond is ~5 percent weaker than the C-F bond, and the C-C1 bond is 25 percent weaker.

In addition to weak chemical bonds, the arrangement of the substituting elements along the polymer chain has a marked effect on the resin's chemical stability. In this regard, solubility can be a leading indicator. Tefzel, with a regularly alternating structure of the monomers tetrafluoroethylene and ethylene, has no known solvent in ordinary conditions. In contrast, polyvinylidene fluoride, the chemical isomer of Tefzel, is soluble in common industrial ketones (e.g., methyl ethyl ketone). Ethylene/trifluoroethylene is soluble in some fluorinated solvents. The substituted polymers are also adversely affected by strong acids and alkalies. Of the three mentioned, Tefzel is compatible with the broadest range of chemicals under a wide range of conditions.

Equal proportions of the comonomers react to produce a polymer where individual monomers alternate regularly along its chain.

Typical properties of Tefzel appear in Table 2. Data in Table 2 and Table 1 show that the polarity and accompanying interpolymer chain attraction enhance the physical properties of the substituted polymer over those of the unsubstituted, fully fluorinated polymer. Note, for example, that Tefzel has about 1.5 times greater strength than Teflon and 2 times greater stiffness.

Tefzel Fluoropolymer Resin
Table 2

Summary and Conclusion
The chemistry and physicochemistry inherent in the fully fluorinated polymer structures allow Teflon FEP and Teflon PFA fluorocarbon resins to provide unique resin component benefits for chemical corrosion resistance. Tefzel fluoropolymer resin comes closer to Teflon than any other partially fluorinated resin, in chemical and electrical properties, while providing enhanced mechanical ruggedness and economical processing.


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