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Transformation of Chlorinated Hydrocarbons Using Aquocobalamin or Coenzyme F430 in Combination with Zero‐Valent Iron
Author(s) -
Morra Matthew J.,
Borek Vladimir,
Koolpe Jonathan
Publication year - 2000
Publication title -
journal of environmental quality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.888
H-Index - 171
eISSN - 1537-2537
pISSN - 0047-2425
DOI - 10.2134/jeq2000.00472425002900030004x
Subject(s) - halogenation , chemistry , reductive dechlorination , substrate (aquarium) , tetrapyrrole , zerovalent iron , chloroform , chloride , inorganic chemistry , organic chemistry , environmental chemistry , nuclear chemistry , biodegradation , adsorption , oceanography , enzyme , geology
More effective methods are necessary for the remediation of soils, sediments, and ground waters contaminated with halogenated organic compounds. Our objective was to determine the feasibility and utility of using a tetrapyrrole‐Fe(0) mixture for reductive dehalogenation of synthetic organic contaminants. Aquocobaiamin or coenzyme F 430 was combined with Fe(0) in aqueous systems containing either a single chlorinated compound or mixtures of chlorinated compounds, and substrate disappearance was monitored using gas chromatography‐mass spectrometry (GC‐MS). Zero‐valent iron effectively dehalogenated CCl 4 at low to neutral pH values, while increases in CCl 4 dehalogenation resulting from inclusion of tetrapyrrole catalysts along with Fe(0) occurred only at basic pH values. Rates of CCl 4 disappearance increased with additional aquocobalamin, but reached a maximum and decreased at higher aquocobalamin concentrations. Overall dehalogenation rates may thus be a function of Fe(0)'s limited reactive surface area. There was a trend for both tetrapyrrole catalysts to promote the disappearance of halogenated compounds in a mixed substrate containing 20 compounds. Studies with five individual substrates likewise showed trends for increased substrate removal with F 430 beyond that for Fe(0) alone. This increase is most important for compounds such as 1,2‐dichloroethane and 1,4‐dichlorobenzene that are not readily dehalogenated by Fe(0). Chloride concentrations in the reaction mixtures indicated that reductive dehalogenation was the dominant process responsible for substrate disappearance. Use of a combination of aquocobalamin or coenzyme F 430 and Fe(0) may effectively promote dehalogenation, thus producing fewer products and more complete dehalogenation of the target substrates than can be achieved using only one of the abiotic reductants alone.