||Catalytic Hydrodechlorination of Polychlorinated Pesticides and Related Substances: An Executive Summary.
||Ebon Research Systems, Silver Spring, Md.;Municipal Environmental Research Lab., Cincinnati, Ohio.
Chlorine organic compounds ;
Chemical reactors ;
Laboratory equipment ;
Chemical reactions ;
Reaction kinetics ;
Mass spectroscopy ;
Environmental chemical substitutes ;
Aroclor 1248 ;
DDE insecticide ;
||Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy.
A study was undertaken of the catalytic conversion of chlorinated pesticides and other undesirable chlorinated compounds to acceptable compounds. This study shows that chlorine can be catalytically removed and replaced by hydrogen to produce relatively non-toxic hydrocarbons. The batch process involves use of a supported nickel catalyst, ethanol as solvent, and sodium hydroxide as an acid-acceptor of the hydrogen chloride by-product. A reactivity sequence is established based on carbon-chlorine bonding wherein olefinic chlorine is the least reactive. Reaction models are determined for Aroclor 1248 and DDE. Removal of ortho-substituted chlorine is the limiting reaction in hydrodechlorination of Aroclor. Aldrin and dieldrin are the most difficult compounds to hydrodechlorinate because of steric hindrance. Removal of aromatic chlorine is the limiting reaction in the hydrodechlorination of DDT and DDE.