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Determination Of The Degradation Mechanism For Polychlorinated Biphenyl Congeners Using Mechanically Alloyed Magnesium/palladium

Polychlorinated biphenyls are a ubiquitous environmental contaminant that can be found today throughout the world in soils and sediments, lakes and rivers, and flora and fauna. PCBs have percolated throughout the food chain, so that almost every human being has a detectable amount of the contaminant within their blood stream. Existing remediation methods include incineration, dredging and landfilling, and microbial degradation, but all of these methods have drawbacks that limit their effectiveness as treatment options. Recently, the use of zero-valent metals as a means of reductive dechlorination has been explored. Using a combination of zero-valent magnesium and catalytic palladium, a successful bimetallic system capable of degrading PCBs has been created and optimized. Determining the mechanism for the reductive dechlorination has proven to be an arduous task, but experimental evidence has suggested three possible radical-type mechanisms for the use Mg/Pd specifically in methanol (as compared to aqueous systems). These possible mechanisms differ in the type of hydrogen species that replaces the chlorine atom on the PCB. Thermodynamic information has also aided in narrowing down which of the suggested pathways is most likely. It appears likely that the hydrogen involved in the dechlorination has the form of a "hydride-like" radical, which is a form of electron-rich atomic hydrogen. According to the literature, Pd catalysts create this species within the first few subsurface layers of the palladium in the presence of molecular hydrogen. Further work will be necessary to confirm that the "hydride-like" radical is actually the species involved in the dechlorination.

Identiferoai:union.ndltd.org:ucf.edu/oai:stars.library.ucf.edu:etd-4471
Date01 January 2008
CreatorsDeVor, Robert
PublisherSTARS
Source SetsUniversity of Central Florida
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
SourceElectronic Theses and Dissertations

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