Role of humic substances in the photodegradation of naproxen under simulated sunlight

- HA inhibited the photodegradation of naproxen thoroughly.
- FA acted as dual roles in the photodegradation of naproxen (NP).
- 3NP∗ and 1O2 account for direct photodegradation of naproxen.
- FA-mediated photodegradation was attributed to 1O2 in aerated solution.

Humic substances (HS) including humic acid (HA) and fulvic acid (FA) are ubiquitous in the natural waters. Although numerous studies documented their role in photodegradation of organic pollutants, the competitive effects of photosensitization and light-screening of HS on the photodegradation of pollutants are not yet clear. In this work, the role of HS in the photodegradation of the pharmaceutical naproxen (NP) was studied under simulated sunlight. The direct photodegradation quantum yield of NP in deionized water was 2.1 × 10−2, and the apparent quantum yields for photosensitized degradation of NP in the presence of FA and HA were 2.3 × 10−4 and 2.6 × 10−5, respectively. Both direct and photosensitized photodegradation decreased with increasing pH, consistent with the trend of singlet oxygen (1O2) reaction rate constants of NP. HA inhibited the photodegradation of naproxen thoroughly. In contrast, FA accelerated the photodegradation of NP at lower substrate concentration and light intensity, and vice versa. Direct photodegradation of NP declined sharply with spectral radiation attenuation of UV region, when HS-mediated photosensitization predominantly accounted for the photodegradation. The direct photodegradation was ascribed to decomposition of excited triplet state of naproxen (3NP∗) and self-sensitization effect involving 1O2. The FA-mediated photodegradation was mainly attributed to 1O2 oxidation in aerated solution. These findings are important for assessing the competitive effects of humic substances on the photodegradation of pollutants under various conditions in natural waters.

84