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Fluoropolymer, PVF

Tedlar Polyvinyl Fluoride, Chemical Properties, Optical Properties, and Weatherability Performance, Jechn ca Bulletin No. 234444B, DuPont Company, October 1995. [Pg.233]

Exposure medium Temp. (°C) Time (days) PDL Resistance note  [Pg.233]

Giaciai Acetic Acid 75 31 10 Room Temperature One Year 10  [Pg.233]

Woishnis and Ebnesajjad. Chemical Resistance of Specialty Thermoplastics. DOI http //dx.doi.Org/10.1016/B978-l-4557-3110-7.00007-5 [Pg.233]


With the exception of two fluoropolymers, PVF and PTFE, the rest of the resins described in this entry can be processed by standard melt-processing techniques, such as injection, transfer and blow molding, extrusion, and rotational molding. Process equipment for fluoropolymers must be made from corrosion resistant alloys because of the corrosive compound that may be produced when fluoropolymers are heated above their melting points. Higher melt viscosity of these resins may require more powder and higher pressure rating equipment. [Pg.1039]

The fluoropolymer family consists of polymers produced from alkenes in which one or more hydrogens have been replaced by fluorine. The most important members of this family are polytetrafluoroethylene (PTFE) (XLVII), polychlorotrifluoroethylene (PCTFE) (XLVIII), poly(vinyl fluoride) (PVF) (XLIX), poly(vinylidene fluoride) (PVDF) (L) copolymers of... [Pg.309]

PVC, another widely used polymer for wire and cable insulation, crosslinks under irradiation in an inert atmosphere. When irradiated in air, scission predominates.To make cross-linking dominant, multifunctional monomers, such as trifunctional acrylates and methacrylates, must be added. Fluoropolymers, such as copol5miers of ethylene and tetrafluoroethylene (ETFE), or polyvinylidene fluoride (PVDF) and polyvinyl fluoride (PVF), are widely used in wire and cable insulations. They are relatively easy to process and have excellent chemical and thermal resistance, but tend to creep, crack, and possess low mechanical stress at temperatures near their melting points. Radiation has been found to improve their mechanical properties and crack resistance. Ethylene propylene rubber (EPR) has also been used for wire and cable insulation. When blended with thermoplastic polyefins, such as low density polyethylene (LDPE), its processibility improves significantly. The typical addition of LDPE is 10%. Ethylene propylene copolymers and terpolymers with high PE content can be cross-linked by irradiation. ... [Pg.185]

Fluoropolymers, such as copolymer of ethylene and tetrafluoroethylene (ETFE), polyvinylidene fluoride (PVDF) and polyvinyl fluoride (PVF), are widely used in wire and cable insulations. They are relatively easy to process and have excellent chemical and thermal resistance, but tend to creep, crack and possess low mechanical stress at temperatures near their melting points. Radiation has been found to improve their mechanical properties and crack resistance.36... [Pg.157]

Fluoro-substituted Polymers. The fluoropolymers were between the first to be studied by the XPS technique because the substitution of F atom(s) in the -CH.-CH - unit induced very large modifications in the XPS core level spectra (shifts up to 8eV) that were easy to detect and interpret. The XPS valence band spectra of similar compounds, namely poly(vinyl fluoride) (PVF), poly(vinylidene fluoride) (PVF2), poly(trifluoroethylene) (PVF3), and poly(tetrafluoroethylene) (PTFE) (26, 27, 28) are also expected to reflect the induction of such strong electronic effects at the valence molecular level. [Pg.182]

Figure 7. XPS valence band spectra of the fluoropolymers PE, PVF, PVF2, PVF3, and PTFE (11)... Figure 7. XPS valence band spectra of the fluoropolymers PE, PVF, PVF2, PVF3, and PTFE (11)...
Fluoropolymers discussed include polytetrafluoro-ethylene (PTFE), perfluoroalkoxy polymer (PFA), fluorinated ethylene-propylene polymer (FEP), ethylene-tetrafluoroethylene copolymer (ETFE), ethylene-chlorotrifluoroethylene copolymer (ECTFE), polychlorotrifluoroethylene (PCTFE), polyvinylidene fluoride (PVDF), and polyvinyl fluoride (PVF). [Pg.1031]

Partially fluorinated fluoropolymers confain hydrogen (H) or other atoms such as chlorine, in addition to fluorine and carbon. The mosf significanf are homopolymers and copolymers of vinylidene fluoride (VDF). There are also copolymers and homopolymers of CTFE, alfhough some have elastomeric properties. Other significant fluoroplastics include ETFE and PVF. [Pg.1031]

This family of plastics has low toxicity and almost no toxicological activity. No fluoropolymers have been known to cause skin sensitivity and irritation in humans. It has been shown that PVF does not cause any skin reaction in human beings. Excessive human exposure to fluoropolymer dust resulted in no toxic effects, although urinary fluoride content increased. ... [Pg.1040]

Polytetrafluoroethylene (PTFE Teflon) was discovered accidently by PlunkettCZ nd commercialized by DuPont in the 1940 s. This polymer has a solubility parameter of about 6H and a high melting point of 327°C and is not readily moldable. Poly-chlorotrifluoroethylene (CTFE, Kel-F), the copolymer of tetrafluoroethylene and hexafluoropropylene (FEP), polyvinylidene fluoride (PVDF, Kynar), the copolymer of tetrafluoroethylene and ethylene (ETFE), the copolymer of vinylidene fluoride and hexafluoroisobutylene (CM-1), perfluoroalkoxyethylene (PFA) and polyvinyl fluoride (PVF, Tedlar) are all more readily processed than PTFE. However, the lubricity and chemical resistance of these fluoropolymers is less than that of PTFE. [Pg.92]

Table 7.2 shows the effect of sodium etching on several fluoropolymers by Tetra-Etch on the surface composition and lap shear bond strength. In general, the data for various fluoropolymers indicate an increase in the adhesive bond strength with increasing fluorine and chlorine content. Kinetics of treatment is more favorable to perfluorinated PTFE than PVF that contains one fluorine per monomer unit according to the data in Table 7.2. [Pg.256]

The most common POM blends are homologous mixtures of POMs having different molecular structures (linear, branched, cross-linked) (Matsuzaki 1991), different molecular weights (Ishida and Sato 1970), or with different end groups (Nagasaki et al. 1991 Hanezawa and Ono 1991). On the secmid place are blends of POM with TPU, preferably polyester type. POMs are also blended with core-shell acrylic elastomers, MBS or MBA. Commercial blends of POM with PEST are available. To improve weatherability of POM, the resin was blended with PMMA and a fluoropolymer (viz. PTFE, PVF, PVDF) (Katsumata 1991). [Pg.102]

For practical purposes there are eight types of fluoropolymers, as summarized in Table F.7. Included in this family of plastics are polytetrafluoroethylene (FIFE), polychlorotrifluoroethylene (PCTFE), polyvinyl fluoride (PVF), fluorinated ethylene propylene (FEP), and others. Depending on which of the fluoropolymers are used, they can be produced as molding materials, extrusion materials, dispersion, film, or tape. Processing of fluoropolymers requires adequate ventilation for the toxic gases (HF) that may be produced. [Pg.211]

Other commercial fluoropolymers (all made by free-radical mechanisms) include polychlorotrifluoroethylene (Kel-F), which is similar to PTFE but which can be moulded at temperatures 300 °C. Polyvinylidene difluoride (PVDF) is a thermoplastic (T 160°C) and films of this material show piezoelectric behaviour. When copolymerized with hexafluropropene a very chemically resistant elastomer is obtained (Viton). Polyvinylfluoride (PVF) is another highly crystalline polymer (T 197°C) which is used for high-performance protective coatings. [Pg.52]

Where unfavorable combinations of chemical, mechanical, and physical environments may preclude the use of other materials, PVF has been successfully used, as for valve and pump parts, heavy wall pipe fittings, gears, cams, bearings, coatings, and electrical insulation. Its limitations include lower service temperatures than the highly fluorinated fluoropolymers, not having antistick qualities, and the fact that it produces toxic products upon thermal decomposition. [Pg.455]

Figure 3.1 Evolution of fluoropolymer development over time. PCTFE, Polychlorotrifluoroethylene PVDF, poly-vinylidene fluoride PVF, polyvinyl fluoride FEP, fluorinated ethylene propylene copolymer ECTFE, ethylene-chlorotrifluoroethylene copolymer ETFE, ethylene-tetrafluoroethylene copolymer PFA, perfluoroalkoxy copolymer AF, amorphous fluoropolymer. Figure 3.1 Evolution of fluoropolymer development over time. PCTFE, Polychlorotrifluoroethylene PVDF, poly-vinylidene fluoride PVF, polyvinyl fluoride FEP, fluorinated ethylene propylene copolymer ECTFE, ethylene-chlorotrifluoroethylene copolymer ETFE, ethylene-tetrafluoroethylene copolymer PFA, perfluoroalkoxy copolymer AF, amorphous fluoropolymer.
A number of properties have to be measured to characterize and identify each fluoropolymer resin. The basic properties of fiuoropoiymers are characterized by standard test methods (Table 5.68) published by the American Society for Testing Materials (ASTM). Five major methods specify types and define properties of fluoropolymer products there is no standard specification method for polyvinyl fluoride (PVF). This section describes each method and the associated tests. Similar documents are published by the International Standards Organization (ISO). [Pg.109]

The commercially important fluorocarbon polymers are poly(tetrafluoroethylene) (PTFE), poly(tetrafluoroethylene-co-hexafluoropropylene) (FEP), poly[tetrafluoroethylene-co-(perfluoroaJkylvinyl ether)] (PFA), and amorphous fluoropolymer (AF), typically copolymers of tetrafluoro-ethylene and fluorinated dioxole. The second group of fluoropolymers includes modified poly(tetrafluoroethylene-co-ethylene) (ETFE), poly(vinylidene fluoride) (PVDF) (sometimes referred to as PVF2), and copolymers of vinylidene fluoride, poly(chlorotrifluoroethylene) (PCTFE), poly(chlorotrifluorethylene-co-ethylene) (E/CTFE) and poly(vinyl fluoride) PVF. [Pg.735]


See other pages where Fluoropolymer, PVF is mentioned: [Pg.66]    [Pg.233]    [Pg.233]    [Pg.1635]    [Pg.1661]    [Pg.1671]    [Pg.66]    [Pg.233]    [Pg.233]    [Pg.1635]    [Pg.1661]    [Pg.1671]    [Pg.13]    [Pg.53]    [Pg.1]    [Pg.18]    [Pg.53]    [Pg.330]    [Pg.96]    [Pg.198]    [Pg.767]    [Pg.39]    [Pg.875]    [Pg.149]    [Pg.833]    [Pg.77]    [Pg.39]    [Pg.882]    [Pg.351]    [Pg.420]    [Pg.360]   


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