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Polytetrafluoroethylene chemical structure

The ignition temperature of a mixture of Ti and C is relatively high compared with those of other pyrolants. When a small amount of polytetrafluoroethylene (Tf) is added to a Ti-C pyrolant, the ignition temperature is significantly lowered due to the exothermic reaction between Ti and Tf Since Tf consists of a -C2F4- chemical structure, the oxidizer gas, F2, is formed by thermal decomposition of Tf according to ... [Pg.321]

Polytetrafluoroethylene (PTFE) has a chemical structure which can be designated by (CF2)k. From its resemblance to the chemical structure of polyethylene it might be thought that the spectra of these two polymers should be quite similar. They do in fact resemble each other, but there are also important differences. This is a consequence of the fact that the PTFE chain configuration is quite different from that of polyethylene, and also the intramolecular forces are undoubtedly significantly different in the two cases. As we shall see, the spectrum is moderately well understood, but not in quite as great detail as that of polyethylene. This is primarily a result of the lack of Raman data on the polymer and certain key polarization data in the infrared. [Pg.115]

Besides the classical polymer introduced by Merrifield (1%-crosslinked chloromethylated polystyrene), a broad variety of polymeric supports is available for SPPS and some of the most popular resins are summarized in Table 1. The chemical structures of some selected resins are presented in Figure 1 and electron micrographs of several examples are displayed in Figure 2. In addition to the solid supports listed in Table 1, there are several other carriers used in peptide synthesis such as the gel-type and macroporous poly(meth-acrylates), coated surfaces like polystyrene films on polyethylene (PEt) sheets, polystyrene-coated polyethylene or polytetrafluoroethylene, and modified glass surfaces. (For recent reviews on polymeric carriers see refs . )... [Pg.672]

Two common liquid membrane support materials, polytetrafluoroethylene and polypropylene, have critical surface tensions of 18 mN/m and 35 mN/m, respectively. Manufacturers often supply critical surface tensions for their porous films. Liquids with a surface tension, y, less than the critical surface tension will probably wet the surface. Therefore, hydrocarbons will wet polypropylene, but water (y = 72 mN/m) will not. Shafrin and Zisman (30) have summarized critical surface tension data for many materials and correlated the data such that critical surface tensions may be estimated from knowledge of the functional groups in the chemical structure of the surface. [Pg.123]

A simple way to frame the issues is to explore the differences between linear polyethylene (PE) and polytetrafluoroethylene— their chemical structures are similar except that in the latter, F has replaced H without destructive distortion of the geometry of the former ... [Pg.9]

Fibers from synthetic polymers make up approximately 80% of the total production of chemical fibers in Germany and about 90% worldwide (2000). The most important synthetic fibers are polyamide (Wulfhorst, 1997), polyester (Tetzlafi", 1997), and polyacrylonitrile (Wulfhorst, 1998). Because of their very specific properties, polyvinyl chloride (Koch, 1968), polytetrafluoroethylene, polyolefin fibers (such as polyethylene and polypropylene) (Wulfhorst, 1989b), and polyvinyl alcohol are used mostly for technical textiles. At the end of this section, an overview is given of synthetic polymers featuring the chemical structures, specific properties, and various applications (Table 2.7). The physical characteristics of chemical fibers from synthetic polymers are summarized later in Table 2.8. [Pg.66]

The general structure of this class of materials can, therefore, be summarized as a fine dispersion of metal oxide in a polymer matrix very similar to plasma polytetrafluoroethylene and in principle any metal should be able to be incorporated. Clearly, if the films are protected from the atmosphere, for metals which form involatile fluorides having a relatively weak metal-fluorine bond strength, it should be possible to produce films having metal atoms dispersed in the matrix. It is expected that these films will have many interesting chemical, optical, electrical and magnetic properties., ... [Pg.39]

Clark, E. S., and L. T. Muus Unusual features in the crystal structure of polytetrafluoroethylene. Meeting of the American Chemical Society, New York, September 1957. [Pg.491]

At the co-deposition of nanocomposite components formation of M/SC particles proceeds simultaneously with formation of a dielectric matrix, and the relationship between these processes determines the nanocomposite structure. This problem has been in detail investigated for the case of M/SC nanoparticles formation in polymer matrices. Synthesis of nanocomposite films by simultaneous PVD of polytetrafluoroethylene (PTFE) and Au has been carried out in works [62-64], Polymer and metal were sputtered under action of Ar ions and then the obtained vapors were deposited on substrates (quartz, glass, silica, mica, etc.) at various temperatures. Here, it is necessary to note that polymer sputtering cannot be considered as only physical process PFTE polymer chains destruct under action of high-energy ions, and formed chemically active low-molecular fragments are then deposited and polymerized on a substrate surface. [Pg.545]

Figure 5.1. Molecular structures of the chemical repeat units for common polymers. Shown are (a) polyethylene (PE), (b) poly(vinyl chloride) (PVC), (c) polytetrafluoroethylene (PTFE), (d) polypropylene (PP), (e) polyisobutylene (PIB), (f) polybutadiene (PBD), (g) c/5-polyisoprene (natural rubber), (h) traw5-polychloroprene (Neoprene rubber), (i) polystyrene (PS), (j) poly(vinyl acetate) (PVAc), (k) poly(methyl methacrylate) (PMMA), ( ) polycaprolactam (polyamide - nylon 6), (m) nylon 6,6, (n) poly(ethylene teraphthalate), (o) poly(dimethyl siloxane) (PDMS). Figure 5.1. Molecular structures of the chemical repeat units for common polymers. Shown are (a) polyethylene (PE), (b) poly(vinyl chloride) (PVC), (c) polytetrafluoroethylene (PTFE), (d) polypropylene (PP), (e) polyisobutylene (PIB), (f) polybutadiene (PBD), (g) c/5-polyisoprene (natural rubber), (h) traw5-polychloroprene (Neoprene rubber), (i) polystyrene (PS), (j) poly(vinyl acetate) (PVAc), (k) poly(methyl methacrylate) (PMMA), ( ) polycaprolactam (polyamide - nylon 6), (m) nylon 6,6, (n) poly(ethylene teraphthalate), (o) poly(dimethyl siloxane) (PDMS).
Polytetrafluoroethylene is a completely fluorinated polymer manufactured by free-radical polymerization of tetrafluoroethylene. With a linear molecular structure of repeating -CF2—CF2- units, PTFE is a crystalline polymer with a melting point of 326.7°C. Its specific gravity is 2.13—2.19. Polytetrafluoroethylene has exceptional resistance to chemicals. Its dielectric constant (2.1) and loss factor are low and stable across a wide range of temperature. It has useful mechanical properties from myogenic temperatures to 260°C. In the United States, PTFE is sold as Halon, Algoflon, Teflon, Fluon, Hostaflon, and Polyflon. ... [Pg.292]


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See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.292 ]




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