首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
The crystal form of TiO_2 is a crucial focus of research on the photocatalytic degradation of gaseous pollutants by TiO_2-based composite photocatalysts. To explore the synergistic effect of mixed crystalline TiO_2 on gaseous organic-pollutant photocatalytic degradation, we synthesized a series of TiO_2 nanoparticles with controllable phase ratios. We explored the role of the TiO_2 phase ratio on the photocatalytic activity and degradation pathway in the photodegradation of 2-propanol(IPA). We estimated the crystallite size and crystal proportions of anatase and rutile by X-ray diffraction. We used the Brunauer-Emmett-Teller method to calculate the specific surface area and Fourier transform infrared spectroscopy to characterize the surface chemistry of the samples. Our results show the photocatalytic activities of pure anatase and the sample with 8.6% rutile to be much better than those of the samples with a phase junction and pure rutile. As such, anatase is the better option for the study of photodegradation design and preparation of gas-phase organic pollutants.  相似文献   

2.
TiO2 nanoparticles(NPs)were prepared via the hydrothermal route of TiO2 xerogel in nitric acid, hydrochloric acid and acetic acid. The physico-chemical properties of the powders were characterized by X-ray diffraction(XRD)and N2 adsorption desorption techniques. The effects of the different acids on the structure(crystal phase)and texture(primary particle size and porosity)of the TiO2 powders were explored. Results indicated that acetic acid facilitated the formation and stability of pure anatase phase. On the other hand, nitric acid and hydrochloric acid led to the transformation from anatase to rutile. The catalyst synthesized via the hydrothermal route of TiO2 xerogel in the low concentration hydrochloric acid solution(Ti-HCl-0.15)had the highest photocatalytic activity than the catalysts obtained in the other two acid solutions. The effects of the different acids were discussed in terms of acid strength, chelating effect and the thermal stability of the adsorbed acidic anions.  相似文献   

3.
An efficient visible-light-responsive BiOBr/TiO2 heterojunction nanocomposite was fabricated successfully using in-situ depositing technique at room temperature by introducing BiOBr onto the surface of TiO2 nanobelts pre-prepared by hydrothermal reaction and etched with H2SO4. The obtained particles were characterized by XRD, SEM, TEM, XPS, UV-Vis DRS and PL techniques. BiOBr/TiO2 heterojunction nanocomposites with different mass ratios of m(BiOBr)/m(TiO2) were discussed in order to get the best photocatalytic activity, and BiOBr/TiO2-1.0 was proved to be the optimal mass ratio. BiOBr/TiO2-1.0 exhibited excellent photocatalytic activity in the degradation of RhB compared with TiO2 nanobelts, pure BiOBr and the mechanical mixture of TiO2 nanobelts and BiOBr. At last, a possible mechanism of photocatalytic enhancement was proposed.  相似文献   

4.
A novel metallo-organic chemical vapor deposition (MOCVD) technique has been applied to the preparation of the photocatalytic titanium dioxide supported on activated carbon. The effects of various condition parameters such as carrier gas flow rate, source temperature and deposition temperature on the deposition rate were investigated. The maximum deposition rate of 8.2 mg/(g·h) was obtained under conditions of carrier gas flow rate of 400 ml/min, source temperature of 423 K and deposition temperature of 913 K. The deposition rate followed Arrhenius behavior at temperature of 753 K to 913 K, corresponding to activation energy E a of 51.09 kJ/mol. TiO2 existed only in anatase phase when the deposition temperature was 773 K to 973 K. With increase of deposition temperature from 1073 K to 1273 K, the rutile content sharply increased from 7% to 70%. It was found that a deposition temperature of 773 K and a higher source temperature of 448 K resulted in finely dispersed TiO2 particles, which were mainly in the range of 10–20 nm. Project (No. 90206007) supported by the National Natural Science Foundation of China  相似文献   

5.
In this study, supported nonmetal (boron) doping TiO2 coating photocatalysts were prepared by chemical vapor deposition (CVD) to enhance the activity under visible light irradiation and avoid the recovering of TiO2. Boron atoms were successfully doped into the lattice of TiO2 through CVD, as evidenced from XPS analysis. B-doped TiO2 coating catalysts showed drastic and strong absorption in the visible light range with a red shift in the band gap transition. This novel B-TiO2 coating photocatalyst showed higher photocatalytic activity in methyl orange degradation under visible light irradiation than that of the pure TiO2 photocatalyst.  相似文献   

6.
A Pr-doped TiO2-NTs/SnO2-Sb electrode was prepared by a simple method, cyclic voltammetry(CV). The methyl orange(MO)aqueous solution was selected as a simulated wastewater. The ordered microstructural TiO2-NTs substrate was synthesized by an electrochemical method to obtain large specific surface area and high space utilization. The phase structure, electrode surface morphology and electrochemical properties of electrodes were characterized by XRD, SEM and electrochemical technology, respectively. The results showed that praseodymium oxide was successfully doped into the SnO2-Sb film by CV method. Due to the doped Pr, the oxygen evolution potential increased from 2.25 V to 2.40 V. The degradation of MO was investigated by UV-vis. The C t /C 0 (φ) was studied as a function to obtain the optimal parameters, such as the amount of doped Pr, current density and initial dye concentration. In addition, the degradation process followed pseudo-first-order reaction kinetics and the rate constant was 0.099 3 min-1. The result indicated that the introduction of Pr reduced the formation of oxygen vacancies or enhanced the formation of adsorbed hydroxyl radical groups on the surface, thus leading to better activity and stability.  相似文献   

7.
采用溶胶-凝胶法,以硝酸铜、二氯化锡和钛酸四丁酯为原料,加入十六烷基三甲基溴化铵(CTAB)作软模板,制备CuO/SnO2/TiO2纳米复合物。分别用SEM、XRD、IR、UV-vis等对产物进行表征分析,CuO/SnO2/TiO2晶粒由锐钛矿相的TiO2、金红石相的SnO2和单斜晶系的CuO组成。以甲基橙为模拟污染物,研究其催化活性,结果表明CuO/SnO2/TiO2纳米复合物具有较好的光催化活性。  相似文献   

8.
The influence of calcination temperature on TiO2 nanotubes' catalysis for TiO2/UV/03 was investigated. TiO2 nanotubes (TNTs) were prepared via the sol-gel method and calcined at 300--700 ℃, which were labeled as TNTs-300, TNTs-400, TNTs-500, TNTs-600 and TNTs-700, respectively. TNTs were characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). It is found that TNTs calcined at 400 ℃ showed the best thermal stability. When the calcination temperature increased from 400 ℃ to 700 ℃, the special structure of tubes was destroyed and gradually converted into nanorods and/or particles. The transformation from anatase to rutile occurred at 600 ℃, and the rutile phase was enhanced when the calcination temperature was increased to over 600 ℃. The calcina- tion temperature's influence on TNTs' adsorption activity for for TiO2/UV/O3 was investigated in landfill leachate solution chemical oxygen demand (COD) and catalytic activity In landfill leachate solution, the adsorption activity of COD decreased in the reduced order of TNTs-300, TNTs-400, TNTs-500, TNTs-600 and TNTs-700. In photocatalytic ozonation, TNTs-400 showed the best catalytic activity while TNTs-700 exhibited the worst. In other three processes, the COD removal of TNTs-300/UV/O3 was higher than those of TNTs-500/UV/O3 and TNTs-600/UV/O3 in the first 20 rain, and then became close to those of the latter two in the following 40 rain. Compared with TNTs-300 and TNTs- 400, TNTs-600 had the best anti-fouling activity, while TNTs-500 and TNTs-700 had lower anti-fouling activity than the former three. In photocatalytic ozonation, the calcination temperature of 400 ℃ was appropriate when TNTs were obtained at the synthesis temperature of 105 ℃.  相似文献   

9.
1Introduction Oxide dilutedmagneticsemiconductors(O DMS)havedrawnmuchattentioninthelastdecadebecause thesematerialsappeartohavegreatpotentialforuse inspin dependentelectronicdevices[1].Recently,iron cobalt dopedtitaniumdioxideswithroomtemperature ferromagnetismhavebeenreported[2].Specially,the resultsofmagneticpropertiesofFexTi1-xO2(x=0.065and0.250)indicatethatferromagnetismwitha Femagneticmomentislargerthantheonereported forCo[3].ThefabricationmethodsofFe Co doped TiO2includepulsedlaser…  相似文献   

10.
ZiO2 was prepared by the hydrolyzation method in (NH4)2SO4-modified TiCl4 solution, and TiO2 photocatalysts were obtained by accelerating the precipitation of TiO2 powder in a high-temperature water bath. The photocatalysts were characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Raman spectrum and UV-Vis (Ultraviolet-Visible) spectrometry techniques, and the photocatalytic activity in phenol-contaminated water was investigated. The results showed that photocatalysts calcined at 400 ℃ had a specific surface area of 138.2 m^2/g and an average particle size of 9 nm, and a significant increase in thermal stability of anatase phase. At the calcination temperature of 700 ~C, the crystal form of TiO2 started to change into rutile (anatase: 97%, rutile: 3%). The activity of TiO2 photocatalysts prepared with (NH4)2SO4-modified TIC14 solution was markedly stronger than that without (NH4)2SOg-modified TIC14 solution. Maximal photocatalytic activity was observed at the mole ratio of Ti:(NH4)2SO4= 1:2, the water-bath temperature of 90℃ and the calcination temperature of 700 ℃.  相似文献   

11.
TiO_2 nanoparticles(NPs)were prepared via the hydrothermal route of TiO_2 xerogel in nitric acid, hydrochloric acid and acetic acid. The physico-chemical properties of the powders were characterized by X-ray diffraction(XRD)and N_2 adsorption desorption techniques. The effects of the different acids on the structure(crystal phase)and texture(primary particle size and porosity)of the TiO_2 powders were explored. Results indicated that acetic acid facilitated the formation and stability of pure anatase phase. On the other hand, nitric acid and hydrochloric acid led to the transformation from anatase to rutile. The catalyst synthesized via the hydrothermal route of TiO_2 xerogel in the low concentration hydrochloric acid solution(Ti-HCl-0.15)had the highest photocatalytic activity than the catalysts obtained in the other two acid solutions. The effects of the different acids were discussed in terms of acid strength, chelating effect and the thermal stability of the adsorbed acidic anions.  相似文献   

12.
The chemisorption properties of N18O adsorption on TiO2(110) surface were investigated by experimental and theoretical methods. The results of temperature programmed desorption (TPD) indicated that the temperatures of the three desorption peaks of the main N2 molecules were at (low) temperature of 230 K, 450 K and (high) temperature of 980 K. This meant that N18O decomposed and recombined during the process of N2 desorption after N18O was exposed. Analysis of the stable combination and orbital theory calculation of the surface reaction of NO adsorption on the TiO2(110) cluster model showed that there was clear preference for the Ti-NO orientation.  相似文献   

13.
Titanium silicalite (TS-1) without and with extra-framework titanium have been prepared and TiO_2 is also prepared under the same conditions.All the samples are characterized with XRD,FT-IR,and UV–Vis.The effects of extra-framework titanium in TS-1 on the ammoximation of cyclohexanone have been studied in a continuous slurry reactor.The characterization results reveal that the extra-framework titanium exists as anatase.The catalytic evaluation results show that the anatase has a positive effect on the ammoximation of cyclohexanone by extending the catalytic life because it also exhibits some activity,while the conversion of cyclohexanone and the selectivity to cyclohexanone oxime are not influenced.The anatase TiO_2 does not catalyze H_2O_2 decomposition appreciably compared with TS-1 without extra-framework titanium.The results are very useful in guiding the TS-1 production.  相似文献   

14.
We first report discovery of the spinel-garnet-orthopyroxene granulite with pure CO2 fluid inclusions from the Fuyun region of the late Paleozoic Altay orogenic belt in Central Asia, NW China. The rock is characterized by an assemblage of garnet, orthopyroxene spinel, cordierite, biotite, plagioclase and quartz. Symplectites of orthopyroxene and spinel, and orthopyroxene and cordierite indicate decompression under UHT conditions. Mineral chemistry shows that the orthopyroxenes have high XMg and Al2O3 contents (up to 9.23 wt%). Biotites are enriched in TiO2 and XMg and are stable under granulite facies conditions. The garnet and quartz from the rock carry monophase fluid inclusions which show peak melting temperatures of around-56.7°C, indicating a pure CO2 species being presented during the ultrahigh-T metamorphism in the Altay orogenic belt. The inclusions homogenize into a liquid phase at temperatures around 15.3–23.8°C translating into CO2 of the order of 0.86–0.88 g/cm3. Based on preliminary minerals paragenesis, reaction textures and petrogenetic grid considerations, we infer that the rock was subjected to UHT conditions. The CO2-rich fluids were trapped during exhumation along a clockwise P-T path following isothermal decompression under UHT conditions. Project supported by the National Basic Research Program (973) of China (No. 2001CB409801), the Exemplary Young Teacher Education and Scientific Research Award Plan of China University, and Postdoctoral Fund of China (No. 2003033033), Postdoctoral Fund of Zhejiang Province, and Starting Fund of Education Ministry, China  相似文献   

15.
Single phase Fe5C2 intermetallic compound was prepared by mechanical alloying method. The phase and crystal structure of sample were analyzed with X-ray differaction spectrum. The decomposing temperature of the Fe5C2 compound is 596.4℃ determined by the DSC curve. It is further shown that the size of nanometer crystal grain is an important condition for carrying out the solid state reaction at room temperature and normal pressure.  相似文献   

16.
The photocatalytic activity of the mixtures of TiO2 with the rare earth oxide La was investigated. The study on the effect of the rare earth oxide content, calcinating temperature and calcinating time on the performance of the mixture revealed that sample treated under higher temperature and longer time had higher photoactivity than pure TiO2. The experimental results of polycrystalline X-ray diffraction showed that the extent of the lattice expansion varied with the variation of calcinating temperature of time. It is suggested that this might be due to the variation of La content diffused into the TiO2 lattice. The La in the lattice may inhibit the recombination of photogenerated electron-hole pairs and thus enhance the photoactivity.  相似文献   

17.
Al-TiO_2介孔材料对溴甲酚绿可见光降解的动力学   总被引:1,自引:0,他引:1  
用固相反应法制得的铝掺杂二氧化钛(Al-TiO2)介孔材料研究了该材料在可见光下对溴甲酚绿的光降解性能及作用因素对降解动力学的影响,探讨了可见光催化的作用机制.结果表明,锐钛矿型的Al-TiO2介孔材料与P25-TiO2粉体对溴甲酚绿溶液的可见光降解行为均遵循准一级反应动力学规律.在298K,pH=6.4、催化剂的用量为1g/L、溴甲酚绿的初始浓度为0.03582mmol/L时,Al-TiO2介孔材料的反应速率常数是P25-TiO2粉体5.2倍;当催化剂的用量为4g/L时,能获得最大的反应速率常数0.09677min-1;溴甲酚绿的初始浓度越低,反应速率常数越大,降解越彻底;温度每升高3℃,Al-TiO2介孔材料的可见光降解反应速率常数依次提高1倍,高于P25-TiO2粉体的增大倍数;在298~304K范围内,Al-TiO2介孔材料对溴甲酚绿可见光降解以空穴氧化为主,其表观活化能比P25-TiO2粉体降低23.7%.  相似文献   

18.
凝胶法制备了Nd离子掺杂TiO2纳米颗粒,采用X射线衍射(XRD)表征了催化剂的晶体结构·以甲基橙为有机底物,测试了Nd掺杂TiO2纳米颗粒光催化活性·结果表明:二氧化钛的主要晶相为锐钛矿相,Nd掺杂可阻止晶相转移·Nd掺杂量为1·5%时,催化活性最高,达到90%以上·  相似文献   

19.
Using SnxTi1-xO2 as carriers, CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 catalysts with different loading amounts of copper oxide (CuO) were prepared by an impregnation method. The catalytic properties of CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 were examined using a microreactor-gas chromatography (GC) NO CO reaction system and the methods of BET (Brun- auer-Emmett-Teller), TG-DTA (themogravimetric and differential thermal analysis), X-ray diffraction (XRD) and H2-temperature programmed reduction (TPR). The results showed that NO conversions of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 were 47.2% and 43.6% respectively, which increased to 95.3% and 90.9% at 6 wt% CuO loading. However, further increase in CuO loading caused a decrease in the catalytic activity. The nitrogen adsorption-desorption isotherm and pore-size distribution curve of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 represented type IV of the BDDT (Brunauer, Deming, Deming and Teller) system and a typical mesoporous sample. There were two CuO diffraction peaks (2θ 35.5° and 38.7°), and the diffraction peak areas increased with increasing CuO loading. TPR analysis also detected three peaks (α, β and γ) from the CuO-loaded catalysts, suggesting that the α peak was the reduction of the highly dispersed copper oxide, the β peak was the reduction of the isolated copper oxide, and the γ peak was the reduction of crystal phase copper oxide. In addition, a fourth peak (δ) of the catalysts meant that the SnxTi1-xO2 mixed oxides could be reductive.  相似文献   

20.
采用溶胶-凝胶法在玻璃表面制得TiO2(锐钛型)薄膜,研究了以254nm的紫外线为光源,酸性品红(AF)在TiO2薄膜上的光催化降解初始速率与溶液初始浓度、初始pH值及外加氧化剂H2O2的关系。结果表明,AF的光催化降解行为采用Langmuir-Hinshelwood(L-H)模型来解释,利用TiO2薄膜作为光催化剂光降有机物AF具有较好的应用前景。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号