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An effective method for the preparation of high temperature stable anatase TiO2 photocatalysts

机译:一种制备高温稳定的锐钛矿型TiO2光催化剂的有效方法

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摘要

An efficient, rapid and straightforward method for the preparation of nitrogen and fluorine (N, F) codoped high temperature stable anatase using a microwave pre-treatment is reported. Using a single source, ammonium fluoride (NH4F) for both nitrogen and fluorine, effective doping of the precursor titanium isopropoxide (TTIP) was possible. These samples were characterised for their structural and optical properties using X-ray diffraction (XRD), Fourier transform IR (FTIR), Raman spectroscopy and UV-vis spectroscopy. In terms of the anatase to rutile transition enhancement using a novel microwave assisted technique, the sample prepared in a composition of 1:8 TiO2: NH4F at 1200 °C was seen to be most effective, having stable anatase present at 57.1 % compared to undoped TiO2 being 100 % rutile from 900 °C. This method involves the production of ammonium oxofluorotitanates (NH4TiOF3) at low temperatures. The inclusion of these intermediates greatly reduces the particle size growth and delays the anatase to rutile transition. The photocatalytic activity of these materials was studied by analysing the degradation of an organic dye, rhodamine 6G as a model system and the rate constant was calculated by pseudo-first-order kinetics. These results showed that the doped sample (0.0225 min-1) was three times more active than the undoped sample (0.0076 min-1) and over seven times faster than the commercial TiO2 photocatalyst standard Degussa P-25 calcined at 1200 °C (0.0030 min-1). The formation of intermediate compounds, oxofluorotitanates, was identified as the major reason for a delay in the anatase to rutile transition.
机译:报道了一种使用微波预处理制备氮和氟(N,F)共掺杂的高温稳定锐钛矿的有效,快速和直接的方法。使用用于氮和氟的单一来源氟化铵(NH4F),可以有效掺杂前驱体异丙氧基钛(TTIP)。使用X射线衍射(XRD),傅里叶变换红外(FTIR),拉曼光谱和紫外可见光谱对这些样品的结构和光学性质进行表征。在使用新型微波辅助技术的锐钛矿到金红石转变的增强方面,以1200:C的1:8 TiO2:NH4F组成制备的样品被认为是最有效的,与未掺杂相比,其锐钛矿的稳定含量为57.1% TiO2在900°C时为100%金红石。该方法涉及在低温下生产氧氟钛酸铵(NH4TiOF3)。这些中间体的加入极大地降低了粒径的增长并延迟了锐钛矿向金红石的转变。通过分析有机染料罗丹明6G作为模型系统的降解,研究了这些材料的光催化活性,并通过拟一级动力学计算了速率常数。这些结果表明,掺杂样品(0.0225 min-1)的活性是未掺杂样品(0.0076 min-1)的三倍,并且比在1200°C(0.0030)下煅烧的商用TiO2光催化剂标准Degussa P-25快七倍以上。 min-1)。中间体化合物氧代氟钛酸盐的形成被认为是从锐钛型到金红石型转变延迟的主要原因。

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