首页> 外文期刊>Journal of Colloid and Interface Science >Enhanced photocatalytic degradation of gaseous toluene and liquidus tetracycline by anatase/rutile titanium dioxide with heterophase junction derived from materials of Institut Lavoisier-125(Ti): Degradation pathway and mechanism studies
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Enhanced photocatalytic degradation of gaseous toluene and liquidus tetracycline by anatase/rutile titanium dioxide with heterophase junction derived from materials of Institut Lavoisier-125(Ti): Degradation pathway and mechanism studies

机译:通过氧化酶/金红石二氧化物与来自Institut Lavoisier-125(TI)的材料的氧化酶/金红石二氧化钛,增强了气态甲苯和液相色谱法的光催化降解了:降解途径和机制研究

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Anatase/rutile titanium dioxide (TiO2) with heterophase junction and large Brunauer-Emmett-Teller (BET) specific surface area (50.1 m(2) g(1)) is successfully synthesized by calcinating Materials of Institut Lavoisier-125(Ti) (MIL-125(Ti)) with 30% O-2/Ar at the temperature of 600 degrees C (M-O-600). Several techniques are used to examine the physicochemical, photoelectrochemical and optical properties of samples, and their photocatalytic performances are evaluated by photodegradation of gaseous toluene and liquidus tetracycline (TC) under visible light illumination. It is found that the calcination temperature has significant influence on the crystal structure and physicochemical parameters of TiO2. The weight fractions of rutile and anatase TiO2 of M-600 are approximately 0.7 and 0.3, which displays outstanding photocatalytic activity. Through the construction of heterophase junction, M-O-600 has better oxygen adsorption and higher density of localized states, which effectively promotes the generation of superoxide radical (center dot O-2(-)) and hydroxyl radical (center dot OH) species. In-situ infrared spectra indicate that toluene is oxidized to benzyl alcohol, benzaldehyde and benzoic acid in turn and then oxidized to formic acid and acetic acid before eventually degraded into H2O and CO2. Gas chromatography-mass spectrometry (GC-MS) is also used to further investigate the degradation pathway of toluene. Degradation pathway and mechanism of TC are studied by liquid chromatography-tandem mass spectrometry (LC-MS). Moreover, three-dimensional excitation-emission matrix fluorescence spectroscopy (3D EEMs) and total organic carbon (TOC) show that TC can be effectively mineralized through a series of reactions by M-O-600 during photocatalysis. (C) 2020 Elsevier Inc. All rights reserved.
机译:采用Lavoisier-125(Ti)(MIL-125(Ti))和30%O-2/Ar在600°C(m-O-600)的温度下煅烧材料,成功合成了具有异质结和大Brunauer-Emmett-Teller(BET)比表面积(50.1 m(2)g(1))的锐钛矿型/金红石型二氧化钛(TiO2)。采用多种技术检测样品的物理化学、光电化学和光学性质,并通过可见光照明下气态甲苯和液相线四环素(TC)的光降解来评估其光催化性能。研究发现,煅烧温度对TiO2的晶体结构和物理化学参数有显著影响。M-600的金红石型和锐钛矿型TiO2的重量分数约为0.7和0.3,显示出优异的光催化活性。通过异质结的构建,M-O-600具有更好的氧吸附和更高的局域态密度,有效地促进了超氧自由基(中心点O-2(-)和羟基自由基(中心点OH)物种的产生。原位红外光谱表明,甲苯依次氧化为苯甲醇、苯甲醛和苯甲酸,然后氧化为甲酸和乙酸,最终降解为H2O和CO2。气相色谱-质谱(GC-MS)也用于进一步研究甲苯的降解途径。采用液相色谱-串联质谱(LC-MS)研究了TC的降解途径和机理。此外,三维激发发射矩阵荧光光谱(3D EEMs)和总有机碳(TOC)表明,在光催化过程中,M-O-600通过一系列反应可以有效矿化TC。(C) 2020爱思唯尔公司版权所有。

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