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1.
采用水热合成-浸渍法制备锌掺杂TiO2纳米管(Zn-TiO2纳米管),透射电镜照片显示Zn-TiO2纳米管为两端开口形貌均一的中空管状结构,管径约6~8 nm,壁厚约1 nm,长度约50~200 nm。研究了Zn-TiO2纳米管对甲基橙的光催化性能,结果表明:掺杂适量锌提高了TiO2纳米管对甲基橙的光催化降解性能,0.4%Zn-TiO2纳米管的光催化性能最佳。同时还探讨了Zn-TiO2纳米管用量和初始pH值等因素对光催化降解甲基橙的影响,结果显示Zn-TiO2纳米管能有效地降解甲基橙。随着光催化反应进行,CODCr去除率和脱色率变化规律不完全相同,可能是由于芳基和烷基降解速率不同所致。  相似文献   

2.
采用溶胶凝胶烧结工艺在玻璃表面制备铅离子多层掺杂的光催化复合TiO2薄膜,用XRD技术表征了该薄膜的晶型,并用电化学方法测定了该薄膜电极的伏安特性及交流阻抗性能.以光催化降解甲基橙溶液为模型反应,采用两种不同方式制备的铅离子多层掺杂TiO2薄膜具有很好的光催化活性,最佳掺杂浓度均为0.5%(Pb/Ti原子百分比),PbD0.5掺铅薄膜的最佳光催化降解甲基橙表观速率常数约是纯TiO2的2.52倍.铅离子掺杂TiO2薄膜表现出近表面处捕获光生电子或空穴,随后被捕获的电子或空穴迁移到TiO2薄膜表向参与光催化反应。  相似文献   

3.
以绢云母为载体,采用水解-沉淀法制备出了绢云母负载纳米TiO2粉体(TiO2/M),以尿素为氮源,采用后掺杂法制得具有可见光响应的N掺杂TiO2/M.采用XRD,XPS,SEM,DUV等手段对样品进行了性能表征;并以日光色镝灯为光源,甲基橙为模拟污染物检测其光催化活性.研究了N的掺杂对粉体中TiO2晶相结构,粒度和光催化性能的影响.结果表明,绢云母与TiO2通过桥氧相连形成包覆层,N的掺杂抑制了TiO2晶粒的长大,减缓锐钛矿向金红石相的转变,同时N的掺杂形成Ti—O—N键,形成新的能级结构,使样品对光的吸收边红移至440—550 nm,具有明显的可见光响应,对甲基橙的光催化降解率与没有掺N的样品相比,最高可达1.6倍.  相似文献   

4.
以P掺杂的TiO2纳米颗粒为前驱体,采用水热合成法制备了系列P掺杂的TiO2纳米管.用N2吸附-脱附、透射电子显微镜(TEM)、X射线衍射(XRD)、激光拉曼光谱(Raman)、紫外可见漫反射(UV-Vis DRS)等方法对光催化材料的表面形貌、颗粒尺寸、孔结构、表面构造、吸光性能进行了分析.研究结果表明,所制备的各样品均为两端开口的纳米管形貌,管长为几十纳米到几百纳米,管外径约10 nm,内径约4 nm,管壁为多层;P掺杂后的系列TiO2纳米管仍保持锐钛矿晶型;掺杂的P可以进入到TiO2的骨架中,并形成P—O—Ti键,在TiO2禁带内引入杂质能级,降低了禁带能量,提高了TiO2的吸光性能及光生电子和空穴的分离性能.光催化甘油水溶液制氢活性评价表明,P掺杂的TiO2纳米管表现出了远高于纯TiO2管以及相同掺杂量的纳米颗粒的光催化制氢性能,2%P掺杂的样品在紫外灯和氙灯辐射下,其最高产氢速率可分别达1850μmol·(h·g)-1和335μmol·(h·g)-1.P掺杂TiO2样品光催化活性的提高与其禁带能量降低以及光生电子和空穴的分离性能增加有关.  相似文献   

5.
以钛酸丁酯为原料,以粉煤灰微珠为载体,采用溶胶-凝胶法制备了TiO2/粉煤灰光催化剂.负载于粉煤灰表面的TiO2平均粒径约为7nm,晶型为锐钛矿型,该催化剂在太阳光下降解初始浓度为10mg·l-1的甲基橙,经6h,甲基橙的降解率可达98.9%,将其应用于实际样品的测定,经3h降解率可达96.1%,显示出优越的光催化降解性能.  相似文献   

6.
张伟  施周  张茜  张骅  徐舜开 《环境化学》2011,30(2):549-554
采用溶胶-凝胶法在不同条件下制备了多壁碳纳米管(MwCNTs)负载纳米TiO2的复合光催化剂(TiO2/MWCNTs).以偶氮类染料甲基橙为模拟污染物,研究不同制备工艺参数的复合光催化剂对甲基橙的光催化降解动力学的影响.对TiO2/MWCNTs的表征结果表明,纳米TiO2较好地分散在多壁碳纳米管表面;随着温度的升高,复...  相似文献   

7.
常温下以TIO2为载体,使用沉积-沉淀法合成了具有不同AgI负载量的AgI/TiO2合光催化剂,并研究了焙烧处理对AgI/TiO2在可见光下(λ>420nm)催化降解甲基橙(MO)的影响.结果表明,焙烧处理有效提高了AgI/TiO2的光催化性能,当焙烧温度高于200℃时,AgI/TiO2的光催化活性接近并达到最大值.当负载的AgI与TiO2的物质的量之比为0.15时,AgI%TiO2光催化降解MO的效率最高.XRD和UV-Vis测试表明焙烧处理提高了光敏组分AgI混晶中的γ相含量,拓宽了AgI/TiO2在可见光区的吸收范围,提高了光催化活性.  相似文献   

8.
叶钊  邱挺  潘海波 《环境化学》2003,22(6):578-581
用超临界二氧化碳萃取TiO2醇凝胶制备纳米二氧化钛粉体,对萃取工艺条件进行了讨论,并用XRD,FT-IR,BET和DRS对上述粉体进行表征.以光催化降解甲基橙为模型反应,结果表明,与超临界二氧化碳干燥所得的粒子比较,该工艺干燥的TiO2粉体粒径小,比表面积大,光催化活性较高。  相似文献   

9.
掺Fe^3+A-TiO2粉末的水热法制备及其光催化降解甲基橙   总被引:1,自引:0,他引:1  
张一兵  郑敏  蒋荣彬  江雷 《生态环境》2010,19(7):1700-1703
以硫酸钛为原料用水热法制备了掺Fe^3+TiO2粉末,用SEM和XRD测定了样品的形貌和晶型,研究了以自制的掺Fe^3+A-TiO2对甲基橙溶液的光催化降解作用。结果表明:所制备的TiO2为锐钛矿型TiO2即A-TiO2。365nm紫外光照射下,用自制的掺Fe^3+A-TiO2降解甲基橙溶液的最佳条件是:10mg·L^-1的甲基橙溶液中加入0.050g掺5%Fe^3+(物质的量比)A-TiO2粉末,用HNO3调节溶液成酸性后,18℃恒温反应4h,降解率达到57.8%。  相似文献   

10.
吴剑涛  柳松 《生态环境》2010,19(5):1054-1058
采用溶胶-凝胶法,将经过油酸铵改性的掺钒二氧化钛粉末投入到纯TiO2溶胶中,烘干、煅烧,制得带有n-n异质结半导体结构的复合型高活性掺钒二氧化钛光催化剂,并通过XRD、TEM、XPS等技术对样品进行了表征。通过对甲基橙溶液的光催化降解实验来考察TiO2/V-TiO2催化剂的光催化活性。结果表明:TiO2/V-TiO2复合催化剂拥有比纯TiO2更高的光催化活性。其中,V的掺杂摩尔分数为0.5%、TiO2:V-TiO2的质量比为10∶1的最佳复合催化剂,其光催化活性是纯TiO2的5.1倍。  相似文献   

11.
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.  相似文献   

12.
Nanosized ZnO rods were synthesized using a microwave-assisted aqueous method. High molecular weight polyvinyl alcohol was used as a stabilizing agent. Size, surface morphology, and structure were investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). SEM and TEM images show that ZnO nanorods have diameters of about 50?nm and lengths of a few micrometers. The XRD pattern reveals that ZnO nanorods are of hexagonal wurtzite structure. The average crystallite size calculated from Scherrer's relation was found to be 40?nm. The effects of catalyst loading, pH value, and initial concentration of methyl orange on the photocatalytic degradation efficiency using ZnO nanorods as photocatalyst were discussed. The results revealed that ZnO nanorods with a diameter of 50?nm showed the highest photocatalytic activity at a surface density of 0.2?g?dm?3.  相似文献   

13.
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.  相似文献   

14.
Nanocrystalline TiO2 films were prepared by magnetron sputtering technique on stainless-steel substrates. The as-deposited TiO2 thin films were in anatase structure with smooth surface morphology. Decomposition of methyl orange was used to measure the photoelectrocatalytic activity. The degradation rate of methyl orange increased with externally applied potential. To further accelerate the photocatalytic reaction, a novel method was employed by applying an external electric field in the mid-frequency domain. The fastest photocatalytic degradation rate of methyl orange was obtained when the frequency was maintained at 20 kHz with an external anodic bias at 3.0 V.  相似文献   

15.
• UV-LED with shorter wavelength was beneficial for photocatalytic degradation. • SRNOM dramatically inhibit the degradation. • ·OH acts as the active radical in photocatalytic degradation. • Degradation mainly undergoes oxidation, hydrolysis and chain growth reactions. In this work, LED-based photocatalysis using mixed rutile and anatase phase TiO2 (P25) as the photocatalyst could effectively remove 5-chloro-2-methyl-4-isothiazolin-3-one (CMIT) and methylisothiazolone (MIT) simultaneously, with removal efficiencies above 80% within 20 min. The photocatalytic degradation of both CMIT and MIT could be modeled using a pseudo-first-order rate equation. The photocatalytic degradation rates of CMIT and MIT under LED280 illumination were higher than under LED310 or LED360 illumination. At concentrations below 100 mg/L, the degradation rate of CMIT and MIT under LED illumination significantly increased with increasing catalyst dosage. Additionally, the effects of the chloride ion concentration, alkalinity and dissolved organic matter on the photocatalytic degradation reaction were also investigated. The ·OH free radicals were determined to play the primary role in the photocatalytic degradation reaction, with a degradation contribution of >95%. The photocatalytic degradation of CMIT and MIT mainly occurred via oxidation, hydrolysis, and chain growth reactions. Finally, the possible photocatalytic degradation pathways of CMIT and MIT over LED/P25 are proposed.  相似文献   

16.
Although nanoscale zero-valent iron (nano-Fe0) is used to remediate pollutants, this reagent still presents stability and reactivity issues. To solve those issues, we synthesized bentonite-supported nanoscale iron bimetals B-Fe/Ni and B-Fe/Pd. We then used those reagents to degrade the methyl orange dye in water. Results of scanning electron microscopy and X-ray diffraction showed that the presence of bentonite and bimetal decreased nanoscale iron aggregation and increased methyl orange removal efficiency. More than 90 % of methyl orange at 100 mg/L was degraded by B-Fe/Ni (0.15 g/L) in 10 min. By comparison, only 62 % of methyl orange was degraded by B-Fe, and 35 % of methyl orange was degraded by nano-Fe0. The degradation rate decreased with the increase of the initial concentration of methyl orange. Lower pH allowed fast removal of methyl orange. Overall our findings show that a nanoscale Fe/Ni on bentonite-supported material is more efficient than nano-Fe0. One-step synthesis is more convenient than current two-step-synthesized nanoscale bimetals. Bentonite-supported nanoscale bimetals could therefore be an economic competitive candidate for contaminated water remediation.  相似文献   

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