Abstract

Visible light photoreduction of toxic Cr(VI) over TiO2 was achieved through surface modification with small molecular weight organic acids (SOAs) as sacrificial organics. Because neat anatase TiO2 is active only under UV light irradiation (λ<387nm), no photoreduction of Cr(VI) was observed in TiO2 dispersions being irradiated with visible light (λ>420nm). However, when a small amount of colorless SOAs was added into the TiO2 dispersion, a charge-transfer-complex (CTC) was formed between TiO2 and SOA, which was sensitive to visible light irradiation and induced the photo-oxidation of SOA and photoreduction of Cr(VI). It was observed that about 95% of added Cr(VI) (0.2mmolL−1) was removed in the visible light-illuminated TiO2 (1.0gL−1) dispersions at pH 3.0 within 2h by adding 0.2mmolL−1 tartaric acid as a SOA. The SOA-induced photoreduction of Cr(VI) proceeded via a CTC-mediated path, being governed by chemical structures of sacrificial SOAs. A higher energy of the highest occupied molecular orbital or lower ionization potential of SOAs is favorable to electron transfer within TiO2-SOA complex, thereby accelerating the photoreduction of Cr(VI). The Cr(VI) removal was further enhanced by increasing SOA concentration and/or decreasing solution pH.

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