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1.
作为光催化技术的核心, 提高TiO2的光催化活性和对可见光的利用率是当前光催化研究中最重要的研究课题. 为了提高TiO2纳米管的可见光催化活性, 采用化学气相沉积法对TiO2纳米管进行了氟掺杂. 扫描电子显微镜(SEM)结果表明退火温度对于TiO2纳米管的形貌完整性有较大影响, 当样品在550和700 °C下退火, 氟掺杂TiO2纳米管结构受损; X射线衍射(XRD)分析表明氟掺杂对TiO2由锐钛矿相转化为金红石相有阻碍作用; X射线光电子能谱(XPS)测试表明化学气相沉积能有效地对TiO2纳米管进行非金属掺杂, 且该方法安全、操作简单. 氟掺杂TiO2纳米管对甲基橙有较高的可见光催化降解活性. 第一性原理计算结果表明氟掺杂对TiO2带隙无显著影响, 费米能级附近的F 2p轨道电子位于价带底部, 与O 2p交联作用较小, 因此对TiO2光吸收带边影响不大. 氟掺杂能促进表面氧空穴的产生, 增加表面酸度与Ti3+, 有利于减少电子-空穴复合率, 从而提高其光催化活性.  相似文献   

2.
以钛酸丁酯为前驱体, 碘溶胶为碘源, 在室温下采用水解沉淀法制备了单质碘和纳米TiO2复合的双介孔结构光催化剂(M-I2-TiO2). 采用X射线衍射(XRD)、透射电子显微镜(TEM)、比表面分析(BET)、紫外-可见(UV-Vis)漫反射光谱和傅里叶变换-红外光谱(FT-IR)对M-I2-TiO2进行了表征. 以次甲基蓝(MB)溶液为模拟废水, 对M-I2-TiO2的光催化性能进行了评价, 研究了不同热处理温度对光催化活性的影响. 结果表明, M-I2-TiO2在可见光区有显著的吸收, 300 ℃热处理得到的样品比表面积高达227.6 m2/g, 600 ℃热处理所得样品的比表面积仍高达111.8 m2/g, 而400 ℃热处理所得样品具有最好的光催化降解性能. 双介孔结构纳米TiO2/I2复合材料的光催化降解性能显著高于相同方法制备的纯TiO2和Degussa P-25商业产品. 催化剂经6次重复使用其光催化活性基本保持不变.  相似文献   

3.
以四氯化钛为钛源,针铁矿(α-FeOOH)为载体,采用水解沉淀法制备了金红石相二氧化钛(Ti2O)与α-FeOOH的复合光催化材料,并采用X射线衍射、扫描电子显微镜、透射电子显微镜、X射线能量散射谱和X射线光电子能谱对样品进行了表征.结果表明,低温下,金红石相Ti2O包覆于α-FeOOH表面,并形成复合结构;较高温下,铁离子进入金红石相Ti2O晶格,并形成铁掺杂金红石相Ti2O纳米管;中温下,样品兼有复合和掺杂两者特征.在室温下以甲基橙为降解对象,采用钨灯+氘灯(波长200~800nm)为光源,对样品的光催化活性进行了测试.结果表明,样品对甲基橙的光催化降解效果良好;与纯α-FeOOH和金红石相Ti2O相比,不同结构样品的光催化活性均有所提高,其中,复合兼掺杂型样品的光催化活性最高.由此可见,与α-FeOOH复合和铁掺杂是提高Ti2O光催化活性的有效途径.  相似文献   

4.
以超强耐酸碱的表面活性剂-丁基封端脂肪醇聚氧乙烯醚作为晶型调节剂,利用钛酸丁酯和氢氧化钠的水热反应制备了单斜相与锐钛矿相双晶相TiO2/多壁碳纳米管(简称MWNTs)复合材料,并考察了复合材料的可见光光催化活性。结果显示:MWNTs的加入可调控TiO2的晶相组成,增强TiO2的光催化活性,其中含5%MWNTs的样品具有较高的催化降解效率;随煅烧温度的升高,样品的光催化活性大幅提升。其机理归因于(1)促进单斜相和锐钛矿相双晶相结构的形成;(2)碳纳米管优良的导电作用及碳纳米管/TiO2间的异质结效应;(3)高温下碳纳米管分解产生的碳元素掺杂作用。  相似文献   

5.
采用水热法合成钛酸钾(K2Ti8O17)纳米棒,并将它作为前驱体水热转晶合成TiO2纳米晶,同时通过在水热体系中引入稀土元素La3+实现对TiO2的La掺杂.考察了不同条件下钛酸盐向TiO2的转晶过程,发现水热溶液的pH值、温度以及预处理步骤对转晶过程有很大的影响.利用X射线衍射以及透射电子显微镜对样品的晶相和形貌进行了表征.利用电感耦合等离子体原子发射光谱测量了所合成的La掺杂TiO2样品中的La含量.通过在紫外光下降解甲基橙(MO,10mg/L)测试了La掺杂TiO2样品的光催化性能.结果表明La掺杂后TiO2的光催化活性大大提高.在0.15mol/LLa3+浓度下180oC水热合成的La掺杂TiO2样品显示了最佳的光催化活性.其对MO的光催化降解反应常数高达0.11min-1,大约是空白TiO2样品的9.20倍,P25TiO2的3.69倍.  相似文献   

6.
阳极氧化法制备TiO2纳米管及其光催化性能   总被引:1,自引:0,他引:1  
纳米TiO2对诸多环境污染物有显著的光催化降解作用,光催化已发展成为新型环境污染治理技术。本文采用阳极氧化法制备出TiO2纳米管,对比了四种电解液组成(A氟化铵+硫酸铵+水;B氟化铵+硫酸铵+乙酸+水;C氟化铵+硫酸铵+甘油+水;D氢氟酸+二甲基亚砜(DMOS)+乙醇)对催化剂表面形貌及光催化性能的影响。结果表明,电解液A和C都制备出了形貌清晰的TiO2纳米管,管径约为60~74 nm。样品经400 ℃煅烧,TiO2晶型主要为锐钛矿相;经500 ℃煅烧,出现少量金红石相;经700 ℃煅烧,晶型全部为金红石相。具有良好形貌的TiO2纳米管同时具有良好的紫外光吸收能力。当亚甲基蓝初始浓度为10 mg·L-1,经500 ℃煅烧的TiO2纳米管光催化活性最佳,光照30 min亚甲基蓝的降解率达89.98%。亚甲基蓝光催化降解反应符合一级反应动力学,反应速率常数为0.079 30。  相似文献   

7.
SnCl4对纳米二氧化钛晶相结构的低温转变控制研究   总被引:3,自引:0,他引:3  
采用二种方法制备了低温下晶相结构可控制转变的纳米二氧化钛。一种方法是采用乙醇作溶剂的溶胶-凝胶法,通过控制SnCl4的添加量,便可在450℃热处理下实现纳米TiO2从纯锐钛矿到不同比例的复合相直至纯金红石相的转变。另一种方法是采用钛酸丁酯为原料直接低温水解,通过加入不同量的SnCl4,制备了具有晶态结构的二氧化钛复合溶胶,在120℃下干燥处理便可实现TiO2从锐钛矿到不同比例的复合相(金红石型、锐钛矿型和板钛矿型)直至纯金红石相的转变,制备所需晶态结构的纳米TiO2。所有样品进行了透射电镜与XRD表征,制备的纳米TiO2及其TiO2-SnO2纳米复合材料颗粒小、分布均匀、分散性好,没有检测到SnO2晶体的X-衍射特征峰。  相似文献   

8.
以钛酸四丁酯为钛源,通过盐酸调制的水热法制备出了具有棒状结构的金红石相纳米TiO2,并进一步进行高温氢化处理. 采用X射线衍射(XRD),透射电镜(TEM),紫外-可见-近红外漫反射(UV-Vis-NIR DRS),电子顺磁共振(EPR)和表面光伏(SPS)等测试手段对样品进行表征,以气相乙醛和液相苯酚为目标污染物考察催化剂的光催化活性. 结果表明:随着高温氢化处理时间的延长,TiO2样品的可见光吸收逐渐增强,其颜色逐渐由白色转变成灰色,这主要与引入的Ti3+/氧空位缺陷有关. 表面光电压谱和羟基自由基测试表明,适当时间的氢化处理有利于光生电荷的分离. 在光催化氧化降解气相乙醛和液相苯酚过程中,经适当时间氢化处理的样品表现出高的可见光催化活性. 并且可见光催化活性的规律与紫外光下的是一致的. 这是因为氢化处理后在导带底下方引入了缺陷能级,拓展了可见光响应. 过度的氢化处理会在TiO2导带下方引入较低的缺陷能级,使光生电荷的复合加剧,导致光催化活性降低.  相似文献   

9.
以纳米TiO2作光催化剂,制备出环境友好的可光催化降解的纳米复合塑料是解决“白色污染”行之有效的方法之一。本文综述了近年来纳米TiO2固相光催化降解固体废弃塑料的研究进展,探讨了TiO2-聚合物复合膜的固相光催化反应机理及光催化降解情况,从对纳米TiO2表面改性以改善其在聚合物中的分散性,对纳米TiO2进行修饰处理以提高其对可见光的吸收,从而提高其光催化效率等方面探讨了可光降解塑料研究存在的问题及应用前景。  相似文献   

10.
以鳞片石墨为原料, 用改进的Hummers法制备氧化石墨烯(GO), 以异丙醇钛为钛源经一步水热法制备得到金红石相TiO2-石墨烯复合材料(rGO-TiO2), 考察了氧化石墨烯用量对复合材料光催化性能的影响. 采用X射线衍射(XRD), 比表面积(BET), 透射电镜(TEM), 扫描电镜(SEM), 拉曼光谱, 紫外-可见(UV-Vis)吸收光谱和荧光光谱(PL)等测试手段对复合材料进行表征. 结果表明: 复合材料中TiO2为针簇状结构的金红石相, 与石墨烯能够均匀复合; 与纯金红石相TiO2相比, 复合材料具有较大的比表面积. 研究了该复合材料在紫外光下对罗丹明B 以及可见光下对甲基橙光降解效果. 当氧化石墨烯浓度为0.5 mg·mL-1时, 制备得到的复合材料rGO-TiO2具有较好的光催化效果.  相似文献   

11.
Nanostructured TiO2 crystals were synthesized by gel to crystalline conversion. The crystals obtained were anatase form of titania averaging in 30 nm particles with an intrinsic band gap of 3.1 eV. The photocatalytic behavior was evaluated for the bactericidal effect in water, contaminated with the indicator organism Escherichia coli. The 100% photoinactivation of E. coli was achieved within 60 min with suspended nano-TiO2. The catalytic activity of synthesized nanosample was observed to be 2.6 times more than that of commercial TiO2 sample referred to as Degussa P-25. The photoinactivation of E. coli was tested with irradiation source of different wavelengths to substantiate the influence of particle size and nano crystallinity on electronic band structure. The photoactivity of nano titania enhanced to 1.625 times when the source of irradiation shifted from 360 to 400 nm while Degussa P-25 showed no change.  相似文献   

12.
Titanium dioxide (TiO2) nanoparticles of both anatase and rutile phases were synthesized by hydrothermal treatment of microemulsions, and their photocatalytic activity for the degradation of X-GL dye was investigated. The only difference between the two methods used was that different acids were added to the microemulsions to make a direct comparison of the photocatalytic activity of the polymorphs possible. UV — Vis reflectance and XRD spectroscopic investigations of these titanium dioxides indicated that a rutile structure could be formed (PR) when hydrochloric acid was used, and anatase formed (PA) when nitric acid was used. The activity of the two polymorphs and P-25 for the photocatalytic degradation of dye in water was also examined. It was found that P-25 consisting of anatase and rutile has the highest activity, and PR consisting of rutile has the lowest. Photodegradation of X-GL in the presence of these different TiO2 particles under air-equilibrated controlled conditions led to the formation of hydrogen peroxide. The formation rate of H2O2 depended on the difference in crystalloid phase. These results indicate that the observed differences in the photocatalytic activity for the three TiO2 photocatalysts are directly related to the formation rate of H2O2.  相似文献   

13.
TiO2 photocatalytic powders were synthesized by a sol–gel combustion synthesis method in which urea was used as the fuel and titanyl nitrate was used as the oxidizer. Various fuel-to-oxidizer ratios were studied for their effects on the combustion phenomena and the properties of the synthesized TiO2. The fuel-to-oxidizer ratio was found to determine the maximum combustion temperature, which in turn affects the specific surface area, crystallite size, and weight fraction of anatase phase of the synthesized TiO2. The synthesized TiO2 all contain carbonaceous species and are either pure anatase or anatase–rutile mixed phase in crystalline structure. The photocatalytic activity of the TiO2 was found to correlate to a certain degree with the specific surface area, crystallite size, weight fraction of anatase phase, and visible and IR absorbances. The mixed phase TiO2 shows a higher photocatalytic activity than the pure anatase phase TiO2 when containing a small fraction (<~25 wt%) of rutile phase but a lower phoyocatalytic activity when containing a large fraction (>~25 wt%) of rutile phase. The synthesized TiO2 all show higher photocatalytic activity than Degussa P25 TiO2. The enhanced photocatalytic activity was attributed mainly to sensitization by the carbonaceous species and larger amounts of hydroxyl group adsorbed on the TiO2 surface.  相似文献   

14.
Visible‐light‐driven plasmonic photocatalyst Ag‐TiO2 nanocomposite hollow spheres are prepared by a template‐free chemically‐induced self‐transformation strategy under microwave‐hydrothermal conditions, followed by a photochemical reduction process under xenon lamp irradiation. The prepared samples are characterized by using scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, N2 adsorption‐desorption isotherms, X‐ray photoelectron spectroscopy, UV/Vis and Raman spectroscopy. Production of ?OH radicals on the surface of visible‐light illuminated TiO2 was detected by using a photoluminescence method with terephthalic acid as the probe molecule. The photocatalytic activity of as‐prepared samples was evaluated by photocatalytic decolorization of Rhodamine B (RhB) aqueous solution at ambient temperature under visible‐light irradiation. The results show that the surface plasmon absorption band of the silver nanoparticles supported on the TiO2 hollow spheres was red shifted, and a strong surface enhanced Raman scattering effect for the Ag‐TiO2 nanocomposite sample was observed. The prepared nanocomposite hollow spheres exhibits a highly visible‐light photocatalytic activity for photocatalytic degradation of RhB in water, and their photocatalytic activity is higher than that of pure TiO2 and commercial Degussa P25 (P25) powders. Especially, the as‐prepared Ag‐TiO2 nanocomposite hollow spheres at the nominal atomic ratio of silver to titanium ( R ) of 2 showed the highest photocatalytic activity, which exceeds that of P25 by a factor of more than 2.  相似文献   

15.
Sulfur doped ZnO/TiO2 nanocomposite photocatalysts were synthesized by a facile sol‐gel method. The structure and properties of catalysts were characterized by X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS), UV‐vis diffusive reflectance spectroscopy (DRS) and N2 desorption‐adsorption isotherm. The XRD study showed that TiO2 was anatase phase and there was no obvious difference in crystal composition of various S‐ZnO/TiO2. The XPS study showed that the Zn element exists as ZnO and S atoms form SO2?4. The prepared samples had mesoporosity revealed by N2 desorption‐adsorption isotherm result. The degradation of Rhodamine B dye under visible light irradiation was chosen as probe reaction to evaluate the photocatalytic activity of the ZnO/TiO2 nanocomposite. The commercial TiO2 photocatalyst (Degussa P25) was taken as standard photocatalyst to contrast the prepared different photocatalyst in current work. The improvement of the photocatalytic activity of S‐ZnO/TiO2 composite photocatalyst can be attributed to the suitable energetic positions between ZnO and TiO2, the acidity site caused by sulfur doping and the enlargement of the specific area. S‐3.0ZnO/TiO2 exhibited the highest photocatalytic activity under visible light irradiation after Zn amount was optimized, which was 2.6 times higher than P25.  相似文献   

16.
Although tremendous effort has been directed to synthesizing advanced TiO2, it remains difficult to obtain TiO2 exhibiting a photocatalytic efficiency higher than that of P25, a benchmark photocatalyst. P25 is composed of anatase, rutile, and amorphous TiO2 particles, and photoexcited electron transfer and subsequent charge separation at the anatase–rutile particle interfaces explain its high photocatalytic efficiency. Herein, we report on a facile and rational hydrothermal treatment of P25 to selectively convert the amorphous component into crystalline TiO2, which is deposited between the original anatase and rutile particles to increase the particle interfaces and thus enhance charge separation. This process produces a new TiO2 exhibiting a considerably enhanced photocatalytic efficiency. This method of synthesizing this TiO2, inspired by a recently burgeoning zeolite design, promises to make TiO2 applications more feasible and effective.  相似文献   

17.
CeO2/TiO2 nanocomposite was synthesized by particulate sol–gel method. The X-ray diffractogram shows the presence of cubic CeO2 and anatase TiO2 in the composite. The high resolution scanning electron micrographs reveal the nanoparticulate nature of the prepared composite. The composite absorbs UV light and exhibits near-band gap emission corresponding to TiO2 and deep level emission due to crystal defects. The Nyquist plot displays two semicircular arcs indicating the material heterogeneity. The physicochemical characteristics of the synthesized nanocomposite are in favour of its application as an ingredient of sunscreen formulations; under UV light the photocatalytic activity of CeO2/TiO2 composite, tested through the degradation of rhodamine B, is very much less than that by pristine anatase TiO2. Reduced adsorption of moisture by the nanocomposite is a possible reason for the observed very low photocatalytic activity.  相似文献   

18.
陈其凤  徐耀  孙予罕 《化学学报》2010,68(4):301-308
为了更好地利用太阳光和提高二氧化钛的光催化性能,以钛酸四正丁酯、正硅酸乙酯、六水合硝酸镍为原料,在高压釜中140℃非水溶剂热反应,所得材料经400℃焙烧制得镍硅共掺杂的二氧化钛光催化剂.所得材料用X射线衍射、氮吸附、透射电镜、X射线光电子能谱、傅里叶变换红外光谱、紫外漫反射等测试手段分析,结果显示所有样品均为锐钛矿型二氧化钛,Si和Ni均掺杂到TiO2体相中,样品具有较大的比表面积,其最大达303.3m2·g-1.在可见光照射下,以降解罗丹明-B为探针反应研究其可见光催化性能,与未掺杂和镍掺杂的二氧化钛相比较,共掺杂的二氧化钛具有更高的可见光催化性能,当Ni/Ti和Si/Ti的物质的量的比分别为0.01和0.20时,可见光催化性能最好.可见光催化性能的提高归因于镍和硅的协同作用.  相似文献   

19.
To address the challenge of treating complex pollutants containing heavy metals and organic compounds,a phenanthroline/TiO2 nanocomposite with rich oxygen vacancy defects was synthesized to integrate the functions of pollutant detection, adsorption, and photocatalytic degradation. The results showed that the nanocomposite could adsorb Cr3+and the process could be transduced into a colorimetric signal for qualitative and quantitative detection. The adsorbed heavy metal also ...  相似文献   

20.
The photocatalytic characteristics of nanostructured TiO2 ultrafine powder with rutile phase produced using the homogeneous precipitation process at low temperatures (HPPLT) were compared with those of commercial P-25 TiO2 powder by flame hydrolysis. The TiO2 powder by the HPPLT showed much higher photoactivity in the removal rate, showing lower pH values in the solution than the P-25 powder when eliminating metal ions such as Pb and Cu from the aqueous metal-EDTA solutions. This can be inferred as the more rapid photo-oxidation or -reduction of metal ions from the aqueous solution, together with relatively higher efficiencies in the use of an electron-hole pair formed on the surface of the TiO2 particles under UV light irradiation. Also, in the view of the TiO2 particle morphology, compared to the well-dispersed spherical P-25 particles, the agglomerated TiO2 secondary particles by the HPPLT consist of acicular typed primary particles with a thickness in the range of 3–7 nm and the primary particles radialize in all directions, which would be more effective to photocatalytic reactions without the large electron-hole recombination on the surface of the TiO2 particle under UV light irradiation. It can be, therefore, thought that the higher photoactivity of the rutile TiO2 powder by the HPPLT in the aqueous solutions results mainly from having a larger surface area by the acicular shaped primary particles with very thin thickness and radialization in all directions.  相似文献   

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