中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2014年
1期
211-220
,共10页
占昌朝%钟明强%陈枫%杨晋涛%曹小华%张旭%刘涛
佔昌朝%鐘明彊%陳楓%楊晉濤%曹小華%張旭%劉濤
점창조%종명강%진풍%양진도%조소화%장욱%류도
溶胶-凝胶法%SO42-/W-TiO2SiO2%介孔%可见光催化
溶膠-凝膠法%SO42-/W-TiO2SiO2%介孔%可見光催化
용효-응효법%SO42-/W-TiO2SiO2%개공%가견광최화
sol-gel method%SO42-/W-TiO2SiO2%mesoporous%visible light photocatalysis
以P123作为模板剂,采用溶胶-凝胶法合成介孔SO42-/W-TiO2@SiO2(WSTS)可见光响应光催化剂。以甲基橙为模型物,考察其在可见光及紫外光区的光催化活性。采用X射线衍射(XRD)、环境扫描电子显微镜(SEM)、高分辨透射电子显微镜(HRTEM)、X 射线光电子能谱(XPS)、低温氮物理吸附(BET)、紫外-可见漫反射光谱(UV-Vis)、傅里叶变换红外光谱(FTIR)、热重分析(TG)和荧光光谱(PL)对样品的结构及性能进行表征。结果表明:W掺杂不但可以提高样品的比表面积、孔容,而且可以抑制晶型从锐钛矿向金红石转变。与光催化剂P25及未掺杂的样品相比,光催化活性明显提高。且W的最佳掺杂量为n(W)/n(Ti)=0.0025,其在可见光(λ>400 nm)和紫外光区辐照40 h和60 min后,甲基橙的脱色率分别是91.7%和98.9%。
以P123作為模闆劑,採用溶膠-凝膠法閤成介孔SO42-/W-TiO2@SiO2(WSTS)可見光響應光催化劑。以甲基橙為模型物,攷察其在可見光及紫外光區的光催化活性。採用X射線衍射(XRD)、環境掃描電子顯微鏡(SEM)、高分辨透射電子顯微鏡(HRTEM)、X 射線光電子能譜(XPS)、低溫氮物理吸附(BET)、紫外-可見漫反射光譜(UV-Vis)、傅裏葉變換紅外光譜(FTIR)、熱重分析(TG)和熒光光譜(PL)對樣品的結構及性能進行錶徵。結果錶明:W摻雜不但可以提高樣品的比錶麵積、孔容,而且可以抑製晶型從銳鈦礦嚮金紅石轉變。與光催化劑P25及未摻雜的樣品相比,光催化活性明顯提高。且W的最佳摻雜量為n(W)/n(Ti)=0.0025,其在可見光(λ>400 nm)和紫外光區輻照40 h和60 min後,甲基橙的脫色率分彆是91.7%和98.9%。
이P123작위모판제,채용용효-응효법합성개공SO42-/W-TiO2@SiO2(WSTS)가견광향응광최화제。이갑기등위모형물,고찰기재가견광급자외광구적광최화활성。채용X사선연사(XRD)、배경소묘전자현미경(SEM)、고분변투사전자현미경(HRTEM)、X 사선광전자능보(XPS)、저온담물리흡부(BET)、자외-가견만반사광보(UV-Vis)、부리협변환홍외광보(FTIR)、열중분석(TG)화형광광보(PL)대양품적결구급성능진행표정。결과표명:W참잡불단가이제고양품적비표면적、공용,이차가이억제정형종예태광향금홍석전변。여광최화제P25급미참잡적양품상비,광최화활성명현제고。차W적최가참잡량위n(W)/n(Ti)=0.0025,기재가견광(λ>400 nm)화자외광구복조40 h화60 min후,갑기등적탈색솔분별시91.7%화98.9%。
The mesoporous SO42-/W-TiO2@SiO2 visible light photocatalysts were synthesized by sol-gel method using P123 as template. The photocatalytic activity of the prepared mesoporous SO42-/W-TiO2@SiO2(WSTS) for methyl orange was investigated under visible and UV light irradiation, respectively. The textural properties and structure of samples were characterized by X-ray diffraction (XRD), environmental scanning electron microscope (SEM), high-resolution transmission electron micro-scope (HRTEM), X-ray photoelectron spectroscopy (XPS), N2 adsorption-desorption measurements (BET), Fourier transform infrared spectroscopy (FTIR), UV-Vis diffuse reflectance spectroscopy, thermogravimetric analysis (TGA) and photoluminescence spectra (PL). The results show that the W doping not only increases the surface area and pore volume of sulfated mesoporous TiO2@SiO2, but also inhibits the phase transition from anatase to rutile. The photo-degradation results reveal that W doping can greatly improve the photocatalytic activity of sulfated TiO2@SiO2 with mesostructure, which is higher than that of undoped samples and the commercially available Degussa P25 titanium dioxide by degradation of methyl orange (MO) aqueous solutions. The optimal W doping is n(W)/n(Ti)=0.002 5 (mole fraction), the alloy expresses higher photocatalytic activity, the discoloration rates are 91.7%and 98.9%under visible light (λ>400 nm) for 40 h and UV light for 60 min, respectively.