The degradation of tributyltin chloride (TBT) photoinduced by iron(III) was
investigated. Upon irradiation at lambda(excitation) >300 nm a photoredox
process was observed, yielding iron(II) and (OH)-O-. radicals. The disappea
rance of TBT was proved to involve only an attack by (OH)-O-. radicals: the
quantum yield of TBT disappearance was determined. A wavelength effect was
observed; the shorter the excitation wavelength, the higher the rate of TB
T disappearance. Most of the photoproducts were identified and the mechanis
m of degradation was elucidated. The main route to degradation is a stepwis
e debutylation of TBT to di- and mono-butyltin with final formation of inor
ganic tin. The complete mineralization of TBT was achieved with long irradi
ation times, leading to innocuous inorganic tin. Copyright (C) 1999 John Wi
ley & Sons, Ltd.