共查询到19条相似文献,搜索用时 140 毫秒
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为拓展二氧化钛对可见光的响应,采用溶胶-凝胶法、水解法制备了碳掺杂二氧化钛粉末。用X射线衍射、比表面分析和紫外-可见光漫反射吸收光谱等方法对制备的样品进行了表征,对可见光照射下的光催化活性进行了测试,并考察了煅烧温度对光催化活性的影响。结果表明:碳掺杂致使二氧化钛在可见光区的光吸收增强,在降解甲基橙的实验中表现出良好的可见光催化活性;随煅烧温度的增加,晶粒增大,可见光催化活性减弱。 相似文献
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《化工中间体》2016,(6)
采用水热法制备出铁掺杂二氧化钛晶体粉末,以红外光谱仪和X射线衍射仪对其结构进行分析,研究光催化剂在可见光或者紫外光的照射下对有机物的催化降解行为,经过红外光谱仪的分析,以水热法制出备的二氧化钛结构中含有大量的羟基成分,具有良好的光催化活性,而经过X射结衍射仪的测试分析,制备出的二氧化钛晶体属于锐钛矿型,另外,在相同条件下,紫外光照射下的甲基紫降解效率要好于可见光,在优化条件下,掺杂2%的铁的二氧化钛晶粉末对甲基紫的最大降解率分别为59.44%和96.12%,不掺杂铁的二氧化钛晶体粉末的光催化降解率分别为26.53%和41.89%,而掺杂8%的铁的二氧化钛晶体粉末的光催化降解率分别为37.57%和48.61%。 相似文献
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通过简单、绿色的一锅法,在水热条件下合成了高活性纳米C@TiO2光催化剂。对样品进行了透射电镜(TEM)分析、X射线能量色散谱分析(EDS)、X射线衍射(XRD)分析、X射线光电子能谱分析(XPS)、紫外可见吸收光谱(UV-Vis)分析、BET分析及在可见光照射下光催化性能测试。结果表明,采用一锅法可以将碳均匀负载在二氧化钛纳米粒子表面;葡萄糖的存在可以抑制金红石矿和板钛矿晶型二氧化钛的产生,有利于形成锐钛矿晶型二氧化钛;XPS结果表明碳未掺杂到二氧化钛晶格中。C@TiO2复合材料可以吸收全光谱范围的可见光,并且在可见光照射下具有良好的光催化活性。分析表明碳与二氧化钛表面的化学作用有效促进了材料的可见光催化性能。此材料合成方法简单、绿色,可见光催化效果好,有较好的工业应用前景。 相似文献
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为了增强纳米二氧化钛薄膜在紫外光下光催化降解罗丹明B溶液的能力,分别采用磁控直流溅射与射频溅射的方法,使用二氧化钛靶材、镍靶材、碳靶材,分别制备了碳非金属掺杂、镍金属掺杂以及镍、碳共掺杂的纳米二氧化钛薄膜,并利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)和紫外可见分光光度计(UV-Vis)进行表征。SEM结果表明,与纯二氧化钛薄膜相比镍、碳共掺杂纳米二氧化钛薄膜晶粒细化,比表面积增大,薄膜表面聚集体为不规则的多边形颗粒状,有利于增大与污染物的接触面积;XRD结果表明该薄膜的晶粒减小,加快了光生电子空穴对的分离;薄膜的吸收极限红移,禁带宽度减小。在紫外光照射下,镍、碳共掺杂纳米二氧化钛薄膜的光催化性能最优,1 h降解了29.54%的罗丹明B溶液。 相似文献
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以ZIF-8为前驱体,采用热解法制备碳掺杂氧化锌。分别研究ZIF-8在350、400、450 ℃下煅烧以及陈化10 min、3 h、24 h对制备原位碳掺杂氧化锌的影响。通过热重(TG)、X射线衍射(XRD)和扫描电镜(SEM)研究样品的形貌和结构;紫外可见漫反射光谱(UV-vis)和光致发光光谱(PL)证明原位碳掺杂氧化锌具有可见光吸收能力和更低的光生载流子复合率;DFT模拟计算表明氧化锌晶格中掺入碳元素能有效减小带隙值。原位碳掺杂氧化锌较纯氧化锌在可见光和紫外光照射下的光催化性能分别提高1.5倍和3.0倍。空穴和羟基自由基是原位碳掺杂氧化锌光催化降解体系的主要活性基团,并由此提出了碳掺杂氧化锌的光催化机理。 相似文献
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掺铁二氧化钛纳米晶的制备及其光催化性能 总被引:4,自引:0,他引:4
通过溶胶-凝胶法室温制备了掺杂铁二氧化钛纳米晶光催化剂。采用透射电子显微镜、X射线衍射仪、能谱元素分析仪、紫外-可见分光光度计等对所得产物进行表征。以甲基橙为目标降解物,对未掺杂的二氧化钛纳米晶及掺杂铁的二氧化钛纳米晶进行了光催化降解性能研究,并对其降解机理进行了分析。结果表明:适量的铁掺杂有利于提高二氧化钛纳米晶的光催化性能和对甲基橙的降解率。铁的最佳掺杂量为25%[Fe占(Ti+Fe)的摩尔分数]。掺杂铁的二氧化钛纳米晶光催化性能优于纯二氧化钛纳米晶,在光照150min后,甲基橙的降解率达75%以上。 相似文献
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Suseung Lee Chang Yeon Yun Mi Sun Hahn Jeongjin Lee Jongheop Yi 《Korean Journal of Chemical Engineering》2008,25(4):892-896
The synthesis and use of carbon-doped TiO2 particles in photocatalysis under visible light are demonstrated. The carbon-doped titania with its mesoporous structure
was prepared by chemical modification and characterized by several techniques including X-ray diffraction, transmission electron
spectroscopy (TEM), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance spectra (EPR), and diffuse reflectance
UV-Vis. absorption spectra, with emphasis on the effect of carbon as a doping compound to the titania. Based on EPR data,
the photocatalytic activity by visible light can be ascribed to the trapping of electrons at interior sites of the carbon-doped
titania between the valence and conduction bands in the titania band structure, and is able to activated by visible light
of a wavelength of up to 550 nm. The photocatalytic activity of the carbon-doped TiO2 nanoparticles was evaluated by examining the decomposition of phenol by irradiation with artificial solar light (>420 nm)
and the results were compared with those using Degussa P25, a commercially available titania nanomaterial. 相似文献
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N,Ce-codoped titania hollow spheres were prepared using carbon spheres as template and using N,Ce-codoped titania nanoparticles as building blocks. The N,Ce-codoped titania nanoparticles were synthesized at low temperature. The prepared hollow spheres were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) and UV-Vis diffuse reflectance spectrum (DRS). The effect of N and Ce content on the physical structure and photocatalytic properties of the as-prepared hollow sphere samples was investigated. The mechanism of photocatalytic degradation of dyes under visible light irradiation was also discussed. 相似文献
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Nitrogen and/or carbon doped titania photocatalysts were prepared by a novel mechanochemical method. The prepared powders possessed two absorption edges around 400 and 540 nm wavelengths and showed excellent photocatalytic ability for nitrogen monoxide oxidation under visible light irradiation. Under the irradiation of visible light of wavelength >510 nm, 37% of nitrogen monoxide could be continuously removed by the carbon and nitrogen co-doped titania prepared by planetary ball milling of P-25 titania-10% hexamethylenetetramine mixture followed by calcination in air at 400?C. 相似文献
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Shun-Huei Wang Ta-Kun Chen K. Koteswara Rao Ming-Show Wong 《Applied catalysis. B, Environmental》2007,76(3-4):328-334
Carbon-doped or carbon-covered titania can enhance photocatalytic performance under visible light. Here we report the first instance of synergistic effect of the carbon incorporation in anatase titania (TiO2−xCx:C) films with both substitutional doping and surface covered characteristics, by reactively co-sputtering Ti metal and graphite targets. The nature of incorporated carbon is characterized by Raman spectroscopy, X-ray photoelectron spectroscopy and transmission electron microscopy. The absorption edge of the carbon incorporated titania thin films shifted from ultraviolet to visible region and directly depended on the carbon content. The photocatalytic performance, e.g., photodegradation of methylene blue (MB), photo-reduction of silver-ions and super hydrophilicity, was greatly enhanced with increasing carbon content. The best photocatalytic activity is obtained in the TiO2−xCx:C film of the most carbon concentration about 9.3 at.% with a degradation rate-constant of 0.108 h−1 for MB under visible-light illumination. 相似文献
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Vendula Houkov Vclav tengl Snejana Bakardjieva Nataliya Murafa Vclav Tyrpekl 《Applied catalysis. B, Environmental》2009,89(3-4):613-619
Nanocrystalline titania particles doped with ruthenium oxide have been prepared by homogenous hydrolysis of TiOSO4 in aqueous solutions in the presence of urea. The synthesized particles were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM), Selected Area Electron Diffraction (SAED) and surface area (BET) and porosity determination (BJH). The photocatalytic activity of Ru-doped titania samples was determined in the gas phase by decomposition of acetone during irradiation at 365 nm and 400 nm. The Ru-doped titania samples demonstrated enhanced photocatalytic activity under visible light. Ruthenium oxide causes the anatase to rutile transformation to occur at lower temperatures and decreasing of band-gap energy of Ru-doped samples. 相似文献
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Fe~(3+)掺杂提高二氧化钛的光催化活性 总被引:1,自引:0,他引:1
采用沉淀-水热的方法制备了Fe3+掺杂的TiO2光催化剂,通过XRD、Raman、XPS、UV-DRS等对催化剂的结构、光学吸收性质等进行了表征,并以罗丹明B为目标污染物对可见光催化活性进行了测试。实验结果表明:所制备的TiO2光催化剂为锐钛矿相结构;Fe3+的掺杂使得TiO2的初始吸收边明显向可见光区域拓宽,并且增强了TiO2在可见光区域的吸收;Fe3+掺杂后TiO2的可见光催化活性显著提高,以掺杂浓度为0.5%的TiO2光催化效果最好,在可见光下6h内可将罗丹明B溶液完全降解,降解率是未掺杂TiO2的4倍。 相似文献
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用水量对溶胶-凝胶法制备氮掺杂纳米二氧化钛的影响 总被引:2,自引:0,他引:2
采用两种用水量的溶胶-凝胶工艺制备了氮掺杂二氧化钛(N-TiO2)纳米颗粒粉末,对样品进行了X射线衍射、透射电子显微镜、X射线光电子能谱及紫外-可见漫反射谱分析,并以甲基橙的光催化降解实验研究了样品的可见光催化性能。结果表明:采用用水多的溶胶-凝胶工艺可获得可见光催化活性高的N-TiO2,且N-TiO2的颗粒粒径较小;由于溶胶中过量的N掺杂剂可在N-TiO2前驱体凝胶离心分离时被去除,可进行较低温度的煅烧,易于获得N掺杂浓度较高的N-TiO2。另外,采用用水多的工艺时,氮掺杂剂对TiO2颗粒的氮化及凝胶化过程也有很大的影响,有些含氮化合物作为掺杂剂可能会明显降低N-TiO2的可见光催化活性。 相似文献