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PHOTODEGRADATION OF METHYLENE BLUE ON VISIBLE LIGHT IRRADIATED TIO_2 IN THE PRESENCE OF NITROGEN MODIFIED ORGANIC MATERIALS

机译:在氮气改性有机材料存在下可见光照射TiO_2的亚甲蓝的光降解

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Introduction Titanium dioxide, particularly in anatase phase has great potential for many applications such as photocatalysis, solar energy conversion, gas sensor and photolysis of water. It is well known that TiO_2 is the best photocatalysts; however, several attends have been used to increase its photoefficiency and among them adding an inert co-adsorbent such as activated carbon (AC). A synergy effect between both solids has been observed in the photocatalytic degradation of model pollutants [1,2]. Our group performed the work on degradation of aromatic molecules such as phenol and 4-chlorophenol on UV-irradiated TiO_2-AC binary materials showing that functionalization of activated carbon's surface plays an important role upon the photoactivity of TiO_2 [3,4]. It was also shown that the both texture and surface pH of activated carbons are responsible to induce remarkable changes in the product distributions during the photooxidation of 4-chlorophenol [5]. Moreover, Lettmann and coworkers suggested that the specific functional groups on the carbon surface can photo-assist the oxidation process occurring at the TiO_2 surface [6]. It has been demonstrated that doping TiO_2 with nitrogen was one of the most effective approaches to improve photocatalytic activity, of TiO_2 on the visible region [7]. Continuing on that, Asahi et al. prepared nitrogen doped TiO_2 films by sputtering TiO_2 in a N_2/Ar gas mixture, and concluded that the doped Ν atoms narrowed the band gap of TiO_2 by mixing Ν 2p and O 2p states, therefore showed photocatalytic activity for the decomposition of organic compound such as acetone and methylene blue in wavelengths up to 550nm [8]. Particularly, it was indicated that MB degradation model experiments showed that the N-doped TiO_2 nanotube arrays presented a significantly enhancement of the photocatalytic activity comparing with the pure TiO_2 nanotube arrays under the visible light irradiation.
机译:引入二氧化钛,特别是在锐钛矿相中具有很大的潜力,许多应用如光催化,太阳能转换,气体传感器和水的光解。众所周知,TiO_2是最好的光催化剂;然而,已经使用了几次出席以增加其光效率,以及它们中加入惰性共吸附剂如活性炭(AC)。在模型污染物的光催化降解中观察到两种固体之间的协同效应[1,2]。我们的小组在紫外线照射的TiO_2-AC二元材料上进行了芳族分子降解的工作,如苯酚和4-氯苯酚,显示活性炭表面的官能化在TiO_2 [3,4]的光照上起重要作用。还表明,活性炭的纹理和表面pH负责在4-氯苯酚的光氧化期间诱导产品分布的显着变化[5]。此外,Lettmann和Codorkers建议碳表面上的特定官能团可以在TiO_2表面进行光辅助氧化过程[6]。已经证明,用氮气掺杂TiO_2是改善可见区域上的TiO_2的最有效方法之一[7]。继续这一点,Asahi等人。通过在N_2 / Ar气体混合物中溅射TiO_2制备氮掺杂的TiO_2膜,并得出结论,掺杂ζ原子通过混合≥2P和O 2P态变窄TiO_2的带隙,因此显示了用于分解有机化合物的光催化活性丙酮和亚甲蓝的波长高达550nm [8]。特别地,表明MB降解模型实验表明,N掺杂的TiO_2纳米管阵列呈现出与可见光照射下的纯TiO_2纳米管阵列相比的光催化活性的显着提高。

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