Aliphatic halogen compounds vinyl chloride

The technology is applicable to chlorinated and nonchlorinated VOCs methyl tertiary butyl ether (MTBE) dichloroethylene (DCE), trichloroethylene (TCE), and tetrachloroethylene (per-chloroethylene, PCE) dichloroethane (DCA) vinyl chloride alcohols ethers ketones and halogenated and nonhalogenated paraffinic, olefinic, aliphatic, and aromatic hydrocarbons. It is very effective at treating benzene, toluene, ethylbenzene, and xylene (BTEX) compounds and any oxygenate, such as acetone or isopropanol. 

NH, NH-, -CN), silicon and olefinic double bonds are more polymerizable while those containing oxygen (e.g. -C=0,-0-,-0H), chlorine, aliphatic hydrocarbon and cyclic hydrocarbons tend to decompose. Brown (13) reported in his studies of a series of vinyl halides that the dihaloethylenes polymerize more rapidly than the corresponding monohalides and that chlorides and bromides polymerize more rapidly than the fluorides. Kobayashi, et. al. (IJ) found that the additons of certain halo-genated compounds to hydrocarbon monomer streams often dramatically increases the polymerization rate. Thus, these halogenated compounds may be considered to act as gas phase catalysts for the plasma polymerization of hydrocarbons. 

---