Affiliation:
1. Chemistry Department, University of Central Florida, Orlando, FL 32817, USA
2. Provectus Environmental Products, Inc., Freeport, IL 61032, USA
Abstract
Chlorinated alkanes were heavily used in a wide range of industrial applications including as degreasers, paint strippers, chemical intermediates, and soil fumigants. These compounds are an environmental concern due to the adverse health effects associated with them and have been detected in environmental matrices including soils and groundwater. Chlorinated alkanes are recalcitrant, and current remediation methods that employ zero-valent iron (ZVI) are unable to directly dehalogenate these compounds, limiting the available approaches for in situ remediation of these widely utilized chemicals. This study employed a novel approach for the remediation of 1,2,3-trichloropropane (TCP), 1,2-dichloropropane (1,2-DCP), 1,3-dichloropropane (1,3-DCP), 1-chloropropane (1-CP), and 1,2-dichloroethane (1,2-DCA) in the presence of ZVI and vitamin B12, a naturally occurring electron mediator. Batch reactions were performed in order to determine a kinetic model for the associated degradation mechanisms. Dechlorination byproducts were confirmed through gas chromatography-mass spectrometry (GC-MS) coupled to a purge and trap. Free chloride was quantified by ion chromatography (IC) utilizing suppressed conductivity detection. In the absence of vitamin B12, reductive dechlorination of chlorinated alkanes was observed to not occur when exposed to only reactive ZVI particles (<5 μm). However, in the presence of ZVI combined with vitamin B12, complete reductive dechlorination was observed and followed a pseudo-first-order reaction.
Funder
UCF Industrial Environmental Research Group