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DOI 10.1007/s11356-017-0006-2

Медицинская библиотека · Environmental science and pollution research international · 2017

Gamma irradiation-induced decomposition of sulfamethoxazole in aqueous solution: the influence of additives, biological inhibitory, and degradation mechanisms.

Wang Jinjin, Guo Ziyan, Shen Xiaoyu, Guo Qingjun, Zhao Yongfu, Zhu Shengnan, Guo Zhaobing

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Аннотация

Sulfamethoxazole (SMX) was decomposed by using gamma irradiation in the presence of different additives such as NO3-, NO2-, Cr(VI), 2-propanol, and tert-butanol. The results demonstrated that NO3-, NO2-, 2-propanol, and tert-butanol inhibited SMX radiolytic removal. However, there existed a synergetic effect for radiolytic removal of the mixture containing SMX and Cr(VI). At an absorbed dose of 150 Gy, the removal percentages of SMX and Cr(VI) in the mixture were 73.5 and 84.6%, respectively, which was higher than the removal percentages of 70.6 and 4.1% for the single component of SMX and Cr(VI). This provides us an insight into treating the combined pollution in micro-polluted water. The SMX radiolytic removal followed a pseudo first-order reaction kinetic model, and the rate constant ratios of ·OH, eaq-, and H· towards SMX radiolysis were 10.4:1:2.9. In addition, 24-h bio-inhibitory to the macroalgae of SMX solution during gamma irradiation reached the maximum of 0.85 at an adsorbed dose of 100 Gy, then gradually decreased with the increasing adsorbed dose. Based on LC-MS analysis and quantum chemical calculation, the degradation intermediates were determined and concluded that SMX radiolytic removal was mainly via ·OH radical attack and direct decomposition of SMX molecule by gamma ray.

Для цитирования: Wang Jinjin, Guo Ziyan, Shen Xiaoyu, Guo Qingjun, Zhao Yongfu, Zhu Shengnan, Guo Zhaobing. Gamma irradiation-induced decomposition of sulfamethoxazole in aqueous solution: the influence of additives, biological inhibitory, and degradation mechanisms.. Environmental science and pollution research international. 2017. DOI: 10.1007/s11356-017-0006-2.

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