Fluorine chlorofluorocarbons

It appears that the ultimate replacements for the high volume chlorofluorocarbon products are to be more highly fluorinated organic chemicals, thus requiring significantly higher volumes of HF in thek manufacture. 

Properties. The physical properties of aHphatic fluorine compounds containing chlorine are similar to those of the PECs or HECs (3,5). They usually have high densities and low boiling points, viscosities, and surface tensions. The irregularity in the boiling points of the fluorinated methanes, however, does not appear in the chlorofluorocarbons. Their boiling points consistently increase with the number of chlorines present. The properties of some CECs and HCECs are shown in Tables 3 and 4. 

CFG = chlorofluorocarbon HCFC = hydrochlorofluorocarbon see Fluorine compounds,organic-aliphatic. 

Chemical removal of surface material is produced through standard bond-breaking reactions. Typically chlorofluorocarbons (CECs) have been used, eg, CECl, CE2CI2, CE Cl, CE4, CHE, C2C1E. Eor example, CE dissociates into E atoms and fluorinated fragments of CE in a plasma ... 

CHLOROFLUOROCARBONS (cFcs) Ofganie substanees eontaining ehlorine and fluorine whieh were... 

Chlorofluorocarbons (CFCs) Aliphatic carbon compounds containing both chlorine and fluorine atoms. 

Fluorinated compounds are frequently referred lo by code, such as F-l 15. To translate this code into a molecular formula, add 90 to 115. The firsl digit of the sum is the number of carbons the second, the number of hydrogens the third, the number ol fluorines chlorines complete the valences (i.e., C2F5CI is F-l 15 = 90 + 115 = 205. or C H Fj). A four-digit number is used for unsaturated molecules. See Tables 14.1-14.3 for the numbering system for chlorofluorocarbons. 

CHLOROFLUOROCARBONS (cFcs) Organic substances containing chlorine and fluorine which were... 

The first reactions of fluorinated olefins in C02 reported by DeSimone et al. involved the free-radical telomerization of 1,1 -difluoroethylene29 and tetrafluor-oethylene.30 This work demonstrated the feasibility of carrying out free-radical reactions of highly electrophilic species in solvents other than expensive fluorocarbons and environmentally detrimental chlorofluorocarbons. The work has since been more broadly applied to the synthesis of tetrafluoroethylene-based, nonaqueous grades of fluoropolymers,31,32 such as poly(tetrafluoroethylene-co-peduoropropylvinyl ether) (Scheme 2). These reactions were typically carried out at between 20 and 40% solids in C02 at initial pressures of between 100 and 150 bars, and 30-35°C (Table 10.1). 

Freon is a commercial trademark for a series of fluorocarbon products used in refrigeration and air-conditioning equipment, as aerosol propellants, blowing agents, fire extinguishing agents, and cleaning fluids and solvents. Many types contain chlorine as well as fluorine, and should be called chlorofluorocarbons (CFCs) [85,86]. 

The trimer of cyanogen chloride, (CNClls reacts with fluorine in the presence of arsenic pentafluoride in chlorofluorocarbon solvent forming the complex [C3N3Cl3F][AsF6]. 

---