Abstract
Photochemical degradation of 3,3′- and 4.4′-dimethylbiphenyls was studied in natural seawater, without photosensitizer and under artificial UV irradiation. The photooxidation process takes place mainly on benzene ring side chains. Photoproduct analysis, carried out by GC-MS, ETIR and GC-FTIR confirm three successive oxidation states of methyl suhstituents: alcohol, aldehyde and carboxylic acids.