Destruction of PCDDs and PCDFs was investigated by using a dehalogenation reagent including a complex of polyethlene glycol, potassium hydroxide and dimethyl sulfoxide.
When reacted at 70°C, 2, 3, 7, 8-T
4CDD, the most highly toxic among PCDD and PCDF isomers, was very effectively decomposed, resulting into the degradation efficiency to be more than 99.9% for 1hour of the reaction time. A similar result was observed under the coexistence of fat impurities, exemplified by butter. In addition, when the dehalogenation method was adapted to O
8CDD or a purified fraction from waste incinerator fly ash including most of PCDD and PCDF isomers, similar degradation efficiency was also recognized.
In the case of O
8CDD degradation, 1, 2, 3, 4, 6, 7, 8-H
7CDD formed with a maximum yield of 0.28%. However, no other toxic tetra- through hexachlorinated isomers with chlorine atoms in 2, 3, 7 and 8 positions of their molecules generated.
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