Si掺杂TiO2纳米管阵列制备、表征及其光催化氧化降解室内典型VOCs

以Na2SiF6/HF为电解液,采用阳极氧化法一步制备了Si掺杂的TiO2纳米管阵列光催化剂,通过SEM、XRD、DRS和EDX等表征手段对制备的催化剂进行了表征,并以甲苯为降解目标物,考察了Si掺杂的TiO2纳米管阵列光催化剂的活性以及各种反应参数对活性的影响.结果表明,TiO2纳米管阵列以锐钛矿和金红石2种晶形存在,Si高分散于TiO2纳米管的管壁上.Si的掺杂提高了TiO2对紫外光的吸收,其禁带宽度与TiO2相比发生了蓝移.Si掺杂的TiO2纳米管阵列具有较大比表面积.当以电解液中Na2SiF6浓度为0.03 mol·L-1,在400℃焙烧1 h制备的Si掺杂的TiO2纳米管阵列为光催化剂时,甲苯的降解率最高,降解率达到60%,与纯TiO2纳米管阵列相比,催化活性提了1倍.     

空间粒子辐射环境下石墨膜力学性能的演变规律

目的将石墨膜置于9×10^5~9×10^7 rad(Si)总剂量下获得辐射改性石墨膜材料,探讨空间粒子辐射作用下石墨膜拉伸强度的演变规律。方法采用SEM、XRD、煅烧分析及XPS等手段分析石墨膜的结构及成分。结果石墨膜为有序堆积的层状结构,层间距为0.3355 nm,碳的质量分数高达99.75%,挥发分的质量分数为0.04%,灰分的质量分数为0.21%,XPS只检测到C1s及O1s峰。石墨膜的平均热膨胀系数为负值,且其峰值仅为-1.33×10^-6/℃,具备出色的结构稳定性。空间粒子辐射环境模拟试验表明,随着辐射剂量的升高,石墨膜的拉伸强度逐渐衰减,在更高剂量辐射下,石墨膜的拉伸强度趋向稳定。通过Raman光谱仪对辐射石墨膜结构的分析,揭示了力学性能的演变机理。结论辐射石墨膜的拉伸强度与其缺陷含量有很大的相关性,未经过辐射的原始石墨膜的缺陷含量最低,其拉伸强度最大,随着石墨膜的缺陷含量逐渐增多,其拉伸强度逐渐降低。     

Rubber sheet strewn with TiO2 particles:Photocatalytic activity and recyclability

A new method for the preparation of rubber sheet strewn with titanium dioxide particles (TiO₂-strewn sheet) is presented. This simple and low cost method is based on the use of TiO₂ powder (Degussa P25) being strewn onto the sheet made from rubber latex (60% HA) through a steel sieve. The characteristic of the TiO₂-strewn sheet was studied by using scanning electron microscopy/energy dispersive X-ray spectrometer (SEM/EDS) and X-ray diffractometer (XRD) techniques. The photocatalytic activity of TiO₂-strewn rubber sheet was evaluated using Indigo Carmine (IC) dye as a model for organic dye pollutant in water. The results showed that the TiO₂-strewn sheet could degrade IC dye solution under UV light irradiation. The effects of pH, initial concentration, and the intensity of UV light on the photodegradation were also investigated. Kinetics of the photocatalytic degradation was of the first-order reaction. The used TiO₂-strewn sheet can be recovered and reused. The recycling uses did not require any cleaning between successive uses and no decline in the photodegradation efficiency was observed compared with freshly prepared TiO₂-strewn sheet.     

Photocatalytic degradation of perfluorooctanoic acid with β-Ga2O3 in anoxic aqueous solution

Perfluorooctanoic acid (PFOA) is a new-found hazardous persistent organic pollutant, and it is resistant to decomposition by hydroxyl radical (HO·) due to its stable chemical structure and the high electronegativity of fluorine. Photocatalytic reduction of PFOA with β-Ga₂O₃ in anoxic aqueous solution was investigated for the first time, and the results showed that the photoinduced electron (e_cb^-) coming from the β-Ga₂O₃ conduction band was the major degradation substance for PFOA, and shorter-chain perfluorinated carboxylic acids (PFCAs, C_nF_2n+1COOH, 1 ≤ n ≤ 6) were the dominant products. Furthermore, the concentration of F^- was measured by the IC technique and defluorination efficiency was calculated. After 3 hr, the photocatalytic degradation efficiency was 98.8% and defluorination efficiency was 31.6% in the presence of thiosulfate and bubbling N₂. The degradation reaction followed first-order kinetics (k = 0.0239 min^-1, t_1/2 = 0.48 hr). PFCAs (C_nF_2n+1COOH, 1 ≤ n ≤ 7) were detected and measured by LC-MS and LC-MS/MS methods. It was deduced that the probable photocatalytic degradation mechanism involves e_cb^- attacking the carboxyl of C_nF_2n+1COOH, resulting in decarboxylation and the generation of C_nF_2n+1·. The produced C_nF_2n+1· reacted with H2O, forming C_nF_2n+1OH, then C_nF_2n+1OH underwent HF loss and hydrolysis to form C_nF_2n+1COOH.     

Photocatalytic degradation of phenanthrene on soil surfaces in the presence of nanometer anatase TiO2 under UV-light

The effect of nanometer anatase TiO₂ was investigated on the photocatalytic degradation of phenanthrene on soil surfaces under a variety of conditions. After being spiked with phenanthrene, soil samples loaded with different amounts of TiO₂ (0 wt.%, 1 wt.%, 2 wt.%, 3 wt.%, and 4 wt.%) were exposed to UV-light irradiation for 25 hr. The results indicated that the photocatalytic degradation of phenanthrene followed the pseudo first-order kinetics. TiO₂ significantly accelerated the degradation of phenanthrene with the half-life reduced from 45.90 to 31.36 hr for TiO₂ loading of 0 wt.% and 4 wt.%, respectively. In addition, the effects of H₂O₂, light intensity and humic acid on the degradation of phenanthrene were investigated. The degradation of phenanthrene increased with the concentration of H₂O₂, light intensity and the concentration of humic acids. It has been demonstrated that the photocatalytic method in the presence of nanometer anatase TiO₂ was a very promising technology for the treatments of soil polluted with organic substances in the future.     

TiO_2光催化氧化处理废水存在的问题和改进方案

结合TiO2光催化氧化技术的基本原理,讨论了该技术在废水处理过程中存在的主要问题以及改进的方案。可以预见TiO2光催化氧化将是一种非常有效的处理技术,为彻底解决废水处理问题提供了新的手段,在环境污染治理方面具有广阔的应用前景。     

TiO2光催化氧化苯酚动力学研究

以中压汞灯为光源,研究了苯酚在ＴｉＯ２水悬浮液中降解动力学,考察了苯酚在起始浓度,气相氧浓度,催化剂投加量（ＴｉＯ２）光强度以及催化剂煅烧温度对苯酚光解速率的影响,揭示了苯酚多相光催化氧化反应的特点,反应过程符合表现一级动力学规律,气相氧的影响为一级,苯酚初始浓度的影响为负一级,在一定光强度下,催化剂的投加量存在一最值值,说明有效光强度,气相氧以及催化剂投加量是光催化氧化反应的关键因素,适当地热处     

Photocatalytic degradation of methyl orange using ZnO/TiO composites

ZnO/TiO₂ composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange (MO) in aqueous suspension under UV irradiation. The composition and surface structure of the catalyst were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscopy (TEM). The degradation efficiencies of MO at various pH values were obtained. The highest degradation efficiencies were obtained before 30min and after 60min at pH 11.0 and pH 2.0, respectively. A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry. Six intermediates were found during the photocatalytic degradation process of quinonoid MO. The degradation pathway of quinonoid MO was also proposed.     

TiO2光催化氧化法处理有机废水实验分析与改进

介绍光催化氧化的基本原理及其对有机物的光催化氧化过程,对二氧化钛光催化氧化法处理有机废水的实验实例进行了分析,提出了提高二氧化钛光催化氧化活性的方法和研究趋势。     

多相光催化反应器中紫外光辐射能分布的研究

研究了多相光催化反应器中紫外光辐射能量的分布 ,其测试系统主要为光导纤维 光栅光谱仪 .结果表明 ,紫外光辐射相对能量在多相光催化反应器中轴向和径向的分布是不均匀的 ,轴向的能量分布是中轴处能量最大 ,远离中轴能量逐渐减弱 ;径向的能量分布是随着径向远离光源而逐渐减弱 .光催化剂对紫外光辐射能的吸收和阻挡作用较大 ,微孔曝气对光辐射能量的衰减影响较小 .光辐射相对能量衰减可用一指数方程表示