Bui Vu K H, Park Duckshin, Tran Vinh V, Lee Go-Woon, Oh Seo Yeong, Huh Yun Suk, Lee Young-Chul
Department of BioNano Technology, Gachon University, 1342 Seongnamdaero, Sujeong-gu, Seongnam-si 13120, Gyeonggi-do, Republic of Korea.
Korea Railroad Research Institute (KRRI), 176 Cheoldobakmulkwan-ro, Uiwang-si 16105, Gyeonggi-do, Republic of Korea.
J Nanosci Nanotechnol. 2018 Sep 1;18(9):6070-6074. doi: 10.1166/jnn.2018.15606.
TiO2 nanoparticles (NPs) with their excellent photocatalytic performance are among the hottest research subjects for environmental-cleanup applications. In the present work, we developed a method of one-pot synthesis of magnesium aminoclay-titanium dioxide [MgAC-TiO2] nanocomposites in ethanol solution and then treated the obtained nanocomposites in a 350 °C muffle furnace for 3 hours. The obtained X-ray diffraction (XRD) patterns confirmed the growth of the anatase TiO2 NPs in the amorphous MgAC phase. In the scanning electron microscopy (SEM) morphological observation, the MgAC-TiO2 nanocomposites exhibited an aggregate form of 246.59 ± 54.20 nm diameter. The synthesis condition entailing loading of 0.3 g MgAC and 5 mL titanium butoxide (TB) (denoted as MgAC [0.3 g]-TiO2 in 40 mL ethanol solution displayed the largest BET surface area, 234.91 m2/g, as well as the largest pore size and pore volume, 6.7131 nm and 0.3942 cm3/g, respectively. Also, MgAC [0.3 g]-TiO2 showed the best photocatalytic performance for methylene blue (MB) on the batch scale under 365 nm wavelength irradiation: a degradation constant rate of 0.0293 min-1, which was ~20-times-better photocatalytic activity than commercial P25. On the pilot scale (100 L), the MgAC [0.3 g]-TiO2 nanocomposite took only ~12 hours to degrade almost MB at 10 ppm concentration. The mechanism of this high photocatalytic activity was determined to be the high rate of adsorption of both MgAC and oxygen vacancies in the anatase phase coupled with the retardation of the rate of recombination of electrons and holes in the TiO2 NPs, the latter proved by photoluminescent quenching tests.
具有优异光催化性能的二氧化钛纳米颗粒(NPs)是环境净化应用领域最热门的研究课题之一。在本工作中,我们开发了一种在乙醇溶液中一锅合成氨基镁粘土 - 二氧化钛[MgAC - TiO2]纳米复合材料的方法,然后将所得纳米复合材料在350°C马弗炉中处理3小时。所得的X射线衍射(XRD)图谱证实了锐钛矿型TiO2 NPs在非晶态MgAC相中的生长。在扫描电子显微镜(SEM)形态观察中,MgAC - TiO2纳米复合材料呈现出直径为246.59±54.20 nm的聚集体形式。合成条件为在40 mL乙醇溶液中负载0.3 g MgAC和5 mL丁醇钛(TB)(表示为MgAC [0.3 g] - TiO2)时,表现出最大的比表面积,为234.91 m2/g,以及最大的孔径和孔体积,分别为6.7131 nm和0.3942 cm3/g。此外,MgAC [0.3 g] - TiO2在365 nm波长照射下对亚甲基蓝(MB)的批量光催化性能最佳:降解常数速率为0.0293 min-1,其光催化活性比商业P25高约20倍。在中试规模(100 L)下,MgAC [0.3 g] - TiO2纳米复合材料仅需约12小时就能降解10 ppm浓度的几乎所有MB。这种高光催化活性的机制被确定为MgAC和锐钛矿相中氧空位的高吸附速率,以及TiO2 NPs中电子和空穴复合速率的减缓,后者通过光致发光猝灭试验得到证明。