Lee Shiuan-Shinn, Lu Chi-Yuan, Wu Min-Chang
Department of Public Health, Chung Shan Medical University Taichung 40201 Taiwan Republic of China
Department of Family and Community Medicine, Chung Shan Medical University Hospital Taichung 40201 Taiwan Republic of China.
RSC Adv. 2018 Jun 18;8(39):22199-22215. doi: 10.1039/c8ra03557a. eCollection 2018 Jun 13.
This study differs from previous studies of TiO/SiO in that 0.5-10 μm microsized TiO-rutile based catalysts (TR catalysts) with varying proportions of titanium and silicon were synthesized using a one-step modified hydrothermal method. At Ti/Si = 1/9, a two-dimensional channel-structured catalyst with a morphology resembling that of SBA-15 was obtained. In contrast, at Ti/Si = 3/7 or 5/5, a three-dimensional porous structure was formed, and Ti-O-Si-C bonds appeared. The structure of the TR catalyst transformed due to the decrease in C-Si bond content and the increase in C-C bond content with increasing Ti/Si ratio. The results indicated that the rutile phase was the main crystal phase of the TR catalyst. The small crystal size and large rutile phase content of the mesoporous TR catalyst contributed to the low band gap energy below 3.0 eV. Under 2 × 10 W lamp irradiation with either UVA or visible light, the three TR catalysts showed better formaldehyde (HCHO) removal efficiency than P25. Furthermore, the Taguchi method was employed to evaluate the catalytic factors by analysis of variance (ANOVA) and S/N ratio. The results revealed the contributions of each of the three factors to HCHO removal efficiency over TR catalysts to be as follows: space velocity (62%), Ti ratio (32%), and time on stream (5%). The TR catalyst with Ti/Si = 1/9 showed good HCHO removal efficiency with a high (787.1 m g) and large pore volume (0.95 cm g) for a residence time of over 2.29 × 10 s under visible light irradiation. Microwave-assisted EG reduction was successfully applied to dope a TR catalyst with nanosized Pt particles in a short synthesis time. After Pt doping, the removal efficiency in the stream improved and stabilized. The Pt particles were Pt and proved effective for improving the photocatalytic removal of HCHO over the TR catalyst by prolonging the separation time of the electron-hole pairs. Overall, the Pt/TR catalyst is a potential material for pollutant removal and can be easily separated from the pollutant removal system since the catalysts are microsized.
本研究与先前关于TiO/SiO的研究不同之处在于,采用一步法改进水热法合成了钛硅比例不同的0.5 - 10μm微米级TiO - 金红石基催化剂(TR催化剂)。在Ti/Si = 1/9时,获得了一种二维通道结构催化剂,其形态类似于SBA - 15。相比之下,在Ti/Si = 3/7或5/5时,形成了三维多孔结构,并且出现了Ti - O - Si - C键。随着Ti/Si比的增加,由于C - Si键含量的减少和C - C键含量的增加,TR催化剂的结构发生了转变。结果表明,金红石相是TR催化剂的主要晶相。介孔TR催化剂的小晶体尺寸和高金红石相含量导致其带隙能量低于3.0 eV。在2×10 W的UVA或可见光照射下,三种TR催化剂对甲醛(HCHO)的去除效率均优于P25。此外,采用田口方法通过方差分析(ANOVA)和信噪比来评估催化因素。结果表明,三种因素对TR催化剂去除HCHO效率的贡献如下:空速(62%)、Ti比例(32%)和反应时间(5%)。Ti/Si = 1/9的TR催化剂在可见光照射下,停留时间超过2.29×10 s时,表现出良好的HCHO去除效率,具有高比表面积(787.1 m²/g)和大孔体积(0.95 cm³/g)。微波辅助乙二醇还原法成功应用于在短合成时间内用纳米级Pt颗粒掺杂TR催化剂。Pt掺杂后,气流中的去除效率提高并稳定。Pt颗粒为Pt,通过延长电子 - 空穴对的分离时间,证明对提高TR催化剂光催化去除HCHO有效。总体而言,Pt/TR催化剂是一种潜在的污染物去除材料,由于催化剂为微米级,可轻松从污染物去除系统中分离出来。