Hydro chlorofluorocarbons HCFCs

The impact of deposition on global distribution has been noted for the CFC replacements hydro-chlorofluorocarbons (HCFCs), the chlorinated solvents tetrachloroethene (PCE), and trichloro-ethene (TCE), as these compounds undergo gas phase oxidation and photochemical degradation, resulting in the formation of carbonyl halides (e.g., CCI2O) and haloacetyl halides (e.g., bromo-, chloro-, and fluoroacetates). As these compounds are polar and water soluble, they are transported via aerosols, rain, and fog, which impacts their tropospheric lifetime and depositional fluxes (Rompp et al., 2001 de Bmyn et al., 1995). It is not clear whether and to what extent there is evidence of latitudinal fractionation of these compounds. 

While less harmful to the environment than CFCs, hydro-chlorofluorocarbons (HCFCs) are stiU ozone-depleting (they are classified as Class II ozone-depleters) and will be phased out by 2020. Hydrofluorocarbons appear to have little or no ozone-depleting effect and are replacing CFCs and HCFCs in refrigerants and aerosol propellants. 

Scheme 2.14 Lewis acid-assisted halogen exchange of chloroalkanes to (hydro)chlorofluorocarbons (CFC and HCFC).

States would spend 160 billion per year on pollution control. In 1996 Ben Lieberman, an environmental research associate with the Competitive Enterprise Institute, estimated that in the United States the cost of the phaseout of chlorofluorocarbons (CFCs) in accordance with the 1987 Montreal Protocol on Substances That Deplete the Ozone Layer could reach 100 billion over the next ten years. Indeed chemical manufacturers had to develop eco-friendly substitutes such as hydrochlorofluorocarbon (HCFC) and hydro-fluorocarbon (HFC), which are more costly to make, and hundreds of millions of pieces of air-conditioning and refrigeration equipment using CFCs had to be discarded. 

Solvents, like contaminants, may be polar or nonpolar. As a general rule, polar solvents dissolve polar residues while nonpolar solvents dissolve nonpolar residues. Thus, ionic residues such as chlorides, salts, acids, acid fluxes, and alkalis are best dissolved and removed with polar solvents such as water, isopropyl alcohol, ethanol, or methylethyl ketone. Greases, oils, silicones, rosin flux, and low-molecular-weight monomers are best dissolved and removed with solvents such as hydrocarbons, Freons , hydrochloro-fluorocarbons, xylene, terpenes, and naphtha. To remove both polar and nonpolar residues, a two-step process using both types of solvents may be used or, more conveniently, an azeotrope mixture of the two solvents can be used in a one-step process. Most of the chlorofluorocarbon solvents (Freons ) and their azeotropes with alcohols, methylene chloride, or ketones are being phased out due to their high ozone-depletion potentials. Solvent blends and azeotropes of hydro-fluoroethers and hydrochlorofluorocarbons (HCFC) are now replacing these solvents. 

---