Polytetrafluoroethylene Compounds

Filled PTFE—production techniques. Granular polytetrafluoroethylene compounds containing fillers are converted into parts by the same molding techniques as those used for neat resin. The compounding techniques aim at producing uniform blends of PTFE with fillers that can be processed in the same molding equipment. The rest of this section describes methods by which compounds can be made. 

Deformation under load of all filled polytetrafluoroethylene compounds decreases in comparison to unfilled resin, as seen in Table 3.13. Combinations of carbon and graphite reduce deformation the most at room and at elevated temperatures. The next effective filler in reducing deformation under load is bronze at 60% by weight. Hardness is increased by the addition of additives, particularly bronze, carbon, and graphite (Table 3.14). 

Electrical properties. Fillers and additives significantly increase the porosity of polytetrafluoroethylene compounds. Electrical properties are affected by the void content as well as the filler characteristics. Dielectric strength drops while dielectric constant and dissipation factor rise. Metals, carbon, and graphite increase the thermal conductivity of PTFE compounds. Tables 3.19 and 3.20 present electrical properties of a few common compounds. 

Polytetrafluoroethylene has a somewhat higher coefficient of expansion than other plastics. This differential expansion can result in leaking of joints when PTFE is combined with other materials. Addition of fillers such as glass, fiber, graphite, bronze, and molybdenum disulfide alters the coefficient of expansion of polytetrafluoroethylene compounds (Table 3.36). A compound containing 25% filler has a coefficient of expansion about half that of the unmodified resin. 

Polytetrafluoroethylene Compounds - Material obtained by intimate mixing of fillers (metallic and nonmetallic) with polytetrafluoroethylene. One or more of polymer properties sueh as eold flow, wear, and surfaee hardness are altered by the addition of fillers. 

Blends of the polysulfone tesia have been made with ABS, poly(ethylene terephthalate), polytetrafluoroethylene (PTFE), and polycarbonate. These ate sold by Amoco under the Miadel trademark. Additional materials ate compounded with mineral filler, glass, or carbon fiber to improve properties and lower price. 

Some authors have suggested the use of fluorene polymers for this kind of chromatography. Fluorinated polymers have attracted attention due to their unique adsorption properties. Polytetrafluoroethylene (PTFE) is antiadhesive, thus adsorption of hydrophobic as well as hydrophilic molecules is low. Such adsorbents possess extremely low adsorption activity and nonspecific sorption towards many compounds [109 111]. Fluorene polymers as sorbents were first suggested by Hjerten [112] in 1978 and were tested by desalting and concentration of tRN A [113]. Recently Williams et al. [114] presented a new fluorocarbon sorbent (Poly F Column, Du Pont, USA) for reversed-phase HPLC of peptides and proteins. The sorbent has 20 pm in diameter particles (pore size 30 nm, specific surface area 5 m2/g) and withstands pressure of eluent up to 135 bar. There is no limitation of pH range, however, low specific area and capacity (1.1 mg tRNA/g) and relatively low limits of working pressure do not allow the use of this sorbent for preparative chromatography. 

Ultraviolet-visible (UV-vis) diffuse reflectance spectra of supported WOx samples and standard W compounds were obtained with a Varian (Cary 5E) spectrophotometer using polytetrafluoroethylene as a reference. The Kubelka-Munk function was used to convert reflectance measurements into equivalent absorption spectra [12]. Spectral features of surface WOx species were isolated by subtracting from the W0x-Zr02 spectra that of pure Z1O2 with equivalent tetragonal content. All samples were equilibrated with atmospheric humidity before UV-vis measurements. 

Many rubber compounds have a tendency to stick in the mould cavity after vulcanisation and require some type of mould release agent. The substances used are surface-active materials such as detergents, soaps, wetting agents, silicone emulsions, aqueous dispersions of talc, mica and fatty acids, applied by spray or brush. Alternatively, dry types based on polytetrafluoroethylene or polyethylene, usually carried in a solvent, can be aerosol applied. An alternative is the addition of an incompatible material to the rubber compound which will bleed to the rubber surface during vulcanisation. 

The first report of the cyclodimerization of fluorinated olefins was provided by Lewis and Naylor,3 working at E.I. DuPont de Nemours Co., in 1947. While studying the pyrolysis of polytetrafluoroethylene (PTFE), the compound octa-fluorocyclobutane was isolated from the pyrolysis off-gas stream. The researchers identified the product and speculated that it was formed by the cyclodimerization... 

While on the subject of fluoroorganic compounds, one cannot overstate the importance of fluoropolymers in modem industry and science. There is hardly anyone around today who has never heard of polytetrafluoroethylene (PTFE) [CF2—CF2] . Housewives who know nothing about fluorine use PTFE-coated frying pans or pots, and know that PTFE makes washing up easier, because virtually nothing sticks to a PTFE-coated utensil. 

Polytetrafluoroethylene (Tf) is a polymeric fluorine compound that consists of a -C2F4- molecular structure,ini which contains a mass fraction of fluorine of 0.75. Tf is insoluble in water and its specific mass is in the range 3550-4200 kg nr in peUe-... 

The most relevant property of stereoregular polymers is their ability to crystallize. This fact became evident through the work of Natta and his school, as the result of the simultaneous development of new synthetic methods and of extensive stractural investigations. Previously, the presence of crystalline order had been ascertained only in a few natural polymers (cellulose, natural rubber, bal-ata, etc.) and in synthetic polymers devoid of stereogenic centers (polyethylene, polytetrafluoroethylene, polyamids, polyesters, etc.). After the pioneering work of Meyer and Mark (70), important theoretical and experimental contributions to the study of crystalline polymers were made by Bunn (159-161), who predicted the most probable chain conformation of linear polymers and determined the crystalline structure of several macromolecular compounds. 

A variety of natural and synthetic materials are used throughout fuel and lubricant systems. Examples include transfer lines, hoses, fan blades, impellers, small gears, housings, and a host of supporting framework. Some plastics can be degraded by fuels, lubricants, additives, and various petroleum-based compounds. The most resistant material is polytetrafluoroethylene (PTFE). Ryton and Viton are less resistant, but are still quite stable in fuel and lubricant systems. Characteristics of PTFE and Ryton are shown below ... 

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