Abstract
We examined the removal and degradation efficiencies of regenerated amorphous iron oxide on tributyltin (TBT) and triphenyltin (TPT) in seawater. It was confirmed that following contact with iron oxide at 20 and 60 °C, the half-lives of TBT and TPT were shortened. These half-lives were from one-thousandth to one-tenth for natural environment conditions. Dibutyltin and benzene were identified as the reaction products from TBT and TPT, respectively, indicating that the degradation pathways were mainly dealkylation and dephenylation. These results indicate that the treatment method by natural energy will enable the economical and rapid reduction of organotin compounds (OTCs). For OTCs in seawater will be adsorbed on the iron oxide by the ebb and flow of the tide and solar energy will be heat source for degradation when iron oxide is prepared in coastal locations.
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