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纳米TiO₂催化剂存在下酸性红B的声催化降解研究及锐钛矿型和金红石型TiO₂粉末催化活性比较

Investigation on the sonocatalytic degradation of acid red B in the presence of nanometer TiO2 catalysts and comparison of catalytic activities of anatase and rutile TiO2 powders.

作者信息

Wang Jun, Jiang Yuefeng, Zhang Zhaohong, Zhang Xiangdong, Ma Teng, Zhang Guan, Zhao Gang, Zhang Peng, Li Ying

机构信息

Department of Chemistry, Liaoning University, Shenyang 110036, PR China.

Department of Chemistry, Liaoning University, Shenyang 110036, PR China.

出版信息

Ultrason Sonochem. 2007 Jul;14(5):545-551. doi: 10.1016/j.ultsonch.2006.09.004. Epub 2006 Oct 30.

Abstract

Here, the nanometer anatase and rutile titanium dioxide (TiO(2)) powders were introduced to act as the sonocatalysts during the ultrasonic degradation of azo dye-acid red B which was chosen as model compound. The ultrasound of low power was used as an irradiation source to induce TiO(2) particles performing catalytic activity. It was found that the processes of sonocatalytic degradation were different between nanometer anatase TiO(2) and nanometer rutile TiO(2). For nanometer anatase TiO(2) catalyst, the acid red B was mainly oxidated by the holes on the surface of nanometer anatase TiO(2) particles, so that the decolorization and degradation happened at the same time. For the nanometer rutile TiO(2) catalyst, the acid red B was mainly oxidated by the *OH radicals from the ultrasonic cavitation, so that the decolorization of azo bond takes place primarily, and then the degradation of naphthyl ring does. The intermediates of acid red B in the presence of nanometer anatase and rutile TiO(2) powders have been monitored by UV-vis spectra and high performance liquid chromatography (HPLC), respectively. All experiments indicated that the degradation effect of acid red B in the presence of nanometer anatase TiO(2) powder was obviously better than that in the presence of nanometer rutile TiO(2) powder. Hence, the method of sonocatalytic degradation for organic pollutants in the presence of nanometer anatase TiO(2) powder is expected to be promising as an advisable choice for the treatment of organic wastewaters in future.

摘要

在此,引入纳米锐钛矿型和金红石型二氧化钛(TiO₂)粉末,在超声降解作为模型化合物的偶氮染料酸性红B的过程中充当声催化剂。使用低功率超声作为辐照源,以诱导TiO₂颗粒发挥催化活性。发现纳米锐钛矿型TiO₂和纳米金红石型TiO₂的声催化降解过程有所不同。对于纳米锐钛矿型TiO₂催化剂,酸性红B主要被纳米锐钛矿型TiO₂颗粒表面的空穴氧化,从而使脱色和降解同时发生。对于纳米金红石型TiO₂催化剂,酸性红B主要被超声空化产生的·OH自由基氧化,从而首先发生偶氮键的脱色,然后是萘环的降解。分别通过紫外可见光谱和高效液相色谱(HPLC)监测了纳米锐钛矿型和金红石型TiO₂粉末存在下酸性红B的中间体。所有实验表明,纳米锐钛矿型TiO₂粉末存在下酸性红B的降解效果明显优于纳米金红石型TiO₂粉末存在下的降解效果。因此,纳米锐钛矿型TiO₂粉末存在下有机污染物的声催化降解方法有望成为未来处理有机废水的明智选择。

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