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61.
62.
Chih Ming M Ya Wen Lee Gui Bing Hong Te Li Su Je Lueng Shie Chang Tang Chang 《环境科学学报(英文版)》2011,23(4):687-692
TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2,
H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption
and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates
from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET
surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%,
and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%,
79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we
found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that
the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of
e ciently decomposing gaseous DCM in air. 相似文献
63.
Visible light responsive N-F-codoped TiO2 photocatalysts exhibit a higher catalytic activity than N-doped TiO2 for the degradation of 4-chlorophenol due to the synergistic effect of nonmetal elements. 相似文献
64.
考察了高温条件下(70℃)牛粪堆肥、土壤、厌氧污泥、腐烂秸秆种接种物利用玉米秸秆水解液的产氢行为。结果表明:牛粪堆肥接种时达到最大的产气量(1355.7mL/L)和氢气产量(608.4mL/L),随后依次为腐烂秸秆、厌氧污泥和土壤。修改的Gompertz方程可以较好描述产氢量随时间变化趋势(R2>0.99)。牛粪堆肥接种时达到最大的产氢潜力(676.0mL/L),而土壤接种时的迟滞时间最小(9.8h)。DGGE图谱显示:不同接种物对应不同的微生物群落结构。Bacillus thermozeamaize,Enterobacter sp.JDM-19和Thermoanaerobacterium polysaccharolyticum strain,KMTHCJT和可能分别是牛粪堆肥,厌氧污泥和腐烂秸秆接种条件下的关键产氢微生物。 相似文献
65.
66.
Photocatalytic ozonation of phenol and oxalic acid (OA) was conducted with a Ag^+/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag^+ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger. It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag+ was easily reduced and deposited on the surface of Tit2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag^+ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants. 相似文献
67.
The photocatalytic degradation of methylene blue(MB) over Fe-doped CaTiO3 under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction(XRD), scanning electron microscope(SEM) equipped with an energy dispersive spectrometer(EDS) system, Fourier transform infrared spectra(FT-IR), and UV-visible diffuse reflectance spectroscopy(DRS). The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO3 in the visible light region. The Fe-doped CaTiO3 exhibited higher photocatalytic activity than CaTiO3 for the degradation of MB.However, the photocatalytic activity of the Fe-doped CaTiO3 was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO3 prepared at500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB(10 ppm)under UV-visible light for 180 min. 相似文献
68.
TiO2/粉煤灰光催化降解双氯芬酸钠研究 总被引:1,自引:0,他引:1
以燃煤电厂外排的废弃物粉煤灰(CFA)为载体,采用混合泥浆法将TiO2负载在CFA的表面,得到一种新型的复合光催化剂TiO2/CFA.对TiO2/CFA进行了扫描电镜分析、X射线衍射分析和氮吸附测试,并以双氯芬酸钠的光催化降解为评价手段,研究了TiO2负载量对TiO2/CFA光催化性能及重复使用性能的影响.结果表明,TiO2负载量的增加有助于提高TiO2/CFA的光催化性能,但当TiO2负载量过高时,CFA上的TiO2在水处理过程中容易脱落,对TiO2/CFA光催化剂的重复使用性能不利.本研究中,最佳的TiO2负载量约为50%,循环使用6次,其光催化降解效率没有明显降低,双氯芬酸钠的降解率均可达70%以上. 相似文献
69.
本文就各种制氢方式中铝-水反应制氢发展进行了浅析,主要分析了铝-水制氢各方法的优劣、发展过程及发展前景,讨论了铝-水反应制氢的可行性。 相似文献
70.
ZnO-PMMA复合材料光催化去除水中低浓度氨氮 总被引:1,自引:0,他引:1
通过水热法制备纳米ZnO,采用热粘固法成功地将其负载于聚甲基丙烯酸甲酯(PMMA)微球表面,并对ZnO-PMMA复合材料光催化去除水中低浓度氨氮的能力进行了考察.同时,探究了负载比例、初始氨氮浓度、催化剂浓度和pH对低浓度氨氮去除效率的影响.实验结果显示,PMMA改善了纳米ZnO的分散性和光催化能力,ZnO-PMMA能够有效地催化去除氨氮废水.在汞灯照射下,当pH=12、温度为30℃时,1 g·L~(-1)的催化剂(ZnO-PMMA)对50 mg·L~(-1)的氨氮废水去除率达到66%,且反应产物硝氮和亚硝氮含量较低,体现了该催化剂具有将氨氮转化为N2的良好的光催化降解能力.同时,纳米材料可以简单方便地回收,减轻了对环境的潜在影响,符合绿色化学的原则. 相似文献