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Carbon tetrafluoride

Representing a two electron covalent bond by a dash (—) the Lewis structures for hydrogen fluoride fluorine methane and carbon tetrafluoride become... [Pg.13]

Carbon and Graphite. Fluorine reacts with amorphous forms of carbon, such as wood charcoal, to form carbon tetrafluoride [75-73-0], CF, and small amounts of other perfluorocarbons. The reaction initiates at ambient conditions, but proceeds to elevated temperatures as the charcoal bums ia fluoriae. [Pg.124]

Specifications and Analytical Methods. Sulfur hexafluoride is made to rigid specifications. Per ASTM D2472-81 (reapproved 1985) (50), the only permissible impurities are traces of air, carbon tetrafluoride (0.05 wt % max), and water (9 ppm by wt max dew point —45° Cmax). [Pg.242]

Initial attempts at reactions between fluorine and hydrocarbons were described as similar to combustion and the reaction products contained mostly carbon tetrafluoride and hydrogen fluoride ... [Pg.273]

Uses. The chemical inertness, thermal stability, low toxicity, and nonflammability of PFCs coupled with their unusual physical properties suggest many useflil applications. However, the high cost of raw materials and manufacture has limited commercial production to a few, small-volume products. Carbon tetrafluoride and hexafluoroethane are used for plasma, ion-beam, or sputter etching of semiconductor devices (17) (see loN implantation). Hexafluoroethane and octafluoropropane have some applications as dielectric gases, and perfluorocyclobutane is used in minor amounts as a dielectric fluid. Perfluoro-1,3-dimethyl cyclohexane is used as an inert, immersion coolant for electronic equipment, and perfluoro-2-methyldecatin is used for... [Pg.283]

Tetrafluoroethylene undergoes addition reactions typical of an olefin. It bums in air to form carbon tetrafluoride, carbonyl fluoride, and carbon dioxide (24). Under controlled conditions, oxygenation produces an epoxide (25) or an explosive polymeric peroxide (24). Trifluorovinyl ethers,... [Pg.349]

In the absence of air, TEE disproportionates violently to give carbon and carbon tetrafluoride the same amount of energy is generated as in black powder explosions. This type of decomposition is initiated thermally and equipment hot spots must be avoided. The flammability limits of TEE are 14—43% it bums when mixed with air and forms explosive mixtures with air and oxygen. It can be stored in steel cylinders under controlled conditions inhibited with a suitable stabilizer. The oxygen content of the vapor phase should not exceed 10 ppm. Although TEE is nontoxic, it may be contaminated by highly toxic fluorocarbon compounds. [Pg.349]

Because PTFE resins decompose slowly, they may be heated to a high temperature. The toxicity of the pyrolysis products warrants care where exposure of personnel is likely to occur (120). Above 230°C decomposition rates become measurable (0.0001% per hour). Small amounts of toxic perfiuoroisobutylene have been isolated at 400°C and above free fluorine has never been found. Above 690°C the decomposition products bum but do not support combustion if the heat is removed. Combustion products consist primarily of carbon dioxide, carbon tetrafluoride, and small quantities of toxic and corrosive hydrogen fluoride. The PTFE resins are nonflammable and do not propagate flame. [Pg.355]

Carbon tetrafluoride [75-73-0] M 88.0, b -15 . Purified by repeated passage over activated charcoal at solid-C02 temperatures. Traces of air were removed by evacuating while alternately freezing and melting. Alternatively, liquefied by cooling in liquid air and then fractionally distilled under vacuum. (The chief impurity originally present was probably CF3CI). [Pg.157]

CARBON TETRAFLUORIDE CARBONYL FLUORIDE CARBONYL SULFIDE CARBOPHENOTHION CARVONE... [Pg.207]

Now let s apply the Lewis model to the organic compounds methane and carbon tetrafluoride. [Pg.13]

Caibon has eight electrons in its valence shell in both methane and carbon tetrafluoride. By forming covalent bonds to four other atoms, carbon achieves a stable electron configuration analogous to neon. Each covalent bond in methane and carbon tetrafluoride is quite strong—comparable to the bond between hydrogens in Fl2 in bond dissociation energy. [Pg.13]

Hydrogen fluoride Fluorine Methane Carbon tetrafluoride... [Pg.13]

Cyanogen gas, CjN has been found in foe gases of outer space. It can react with fluorine to form carbon tetrafluoride and nitrogen trifluoride. [Pg.70]

B.14 (a) Determine the total number of protons, neutrons, and electrons in one carbon tetrafluoride molecule, CF4, assuming that all atoms are the most common isotopes of that element, (b) What is the total mass of protons, of neutrons, and of electrons in one carbon tetrafluoride molecule Calculate three masses. [Pg.46]

Model A cannot be eliminated definitely by the photographs there are, however, some points which make this model improbable. From the curve for this model the first minimum would be expected to be at least as well pronounced as the second minimum, whereas on the photographs the first minimum is not very well defined. That the qualitative appearance of the photographs supports model C rather than model A is further shown by the fact that the photographs resemble those of methyl nitrate more closely than those of carbon tetrafluoride. Some evidence is also provided by the radial distribution curve (Fig. 1), the first peak being displaced by 0.15 A. from the position expected for it for model A. For these reasons and the additional reason that it is difficult to correlate the tetrahedral configuration with an electronic structure involving only completed octets, we consider model A not to be satisfactory.7... [Pg.639]


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CARBON TETRAFLUORIDE.12(Vol

CF4 Carbon tetrafluoride

Carbon tetrafluoride bonding

Carbon tetrafluoride disposal

Carbon tetrafluoride physical properties

Carbon tetrafluoride production

Carbon tetrafluoride, appearance

Carbon tetrafluoride, bond dissociation energy

Carbon tetrafluoride, from decomposition

Carbon tetrafluoride, reaction

Carbon tetrafluoride-hydrogen

Carbon tetrafluoride-methane

F4C Carbon tetrafluoride

Fluorine compounds carbon tetrafluoride

For carbon tetrafluoride

Oxygen-carbon tetrafluoride

Oxygen-carbon tetrafluoride reactions

PHYSICAL AND CHEMICAL DATA Tables 2-202 Saturated Carbon Tetrafluoride

Saturated Carbon Tetrafluoride

Tetrafluoride

Tetrafluorides

With carbon tetrafluoride

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