Abstract

Photolysis of aqueous solutions of chlorophenols (4-chlorophenol, 2,4-dichlorophenol, 2,4,5-trichlorophenol and pentachlorophenol) in the presence of immobilized non-transition metal phthalocyanine photosensitizers onto Amberlite ® is presented. The photosensitizers studied are: Al (AlOCPc) and Zn (ZnOCPc) octacarboxyphthalocyanines; Al (AlPcS 4) and Zn (ZnPcS 4) tetrasulfophthalocyanines; sulfonated phthalocyanine complexes (containing mixtures of differently substituted derivatives) of Al (AlPcS mix), Zn (ZnPcS mix), Ge (GePcS mix), Si (SiPcS mix) and Sn (SnPcS mix). Photolysis of the chlorophenols resulted mainly in the formation of chlorobenzoquinone derivatives. The complexes showed order of activity towards the transformation of pentachlorophenol as follows: ZnOCPc > SiPcS mix > SnPcS mix > ZnPcS mix > GePcS mix > ZnPcS 4 > AlPcS mix > AlOCPc > AlPcS 4. The generation of singlet oxygen ( 1O 2) by these immobilized MPc photosensitizers was found to play a major role in their photoactivities towards the transformation of these chlorophenols. Langmuir–Hinshelwood (L–H) kinetic model studies showed that the ZnOCPc, GePcS mix and ZnPcS mix photocatalysis occurred on the catalysts surface.

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