催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2013年
12期
2263-2270
,共8页
何霏%马芳%李涛%李光兴
何霏%馬芳%李濤%李光興
하비%마방%리도%리광흥
氮掺杂二氧化钛%溶剂热合成%光催化降解%气相苯%光催化机理
氮摻雜二氧化鈦%溶劑熱閤成%光催化降解%氣相苯%光催化機理
담참잡이양화태%용제열합성%광최화강해%기상분%광최화궤리
N-doped TiO2%Solvothermal synthesis%Photocatalytic degradation%Gaseous benzene%Photocatalytic mechanism
采用三种不同的氮源溶剂热合成了锐钛矿-板钛矿混晶的N-TiO2催化剂。采用X射线衍射、N2吸附-脱附、X射线光电子能谱和透射电子显微镜等手段对催化剂进行了表征。重点研究了不同氮源对催化剂的相组成、晶粒尺寸、微观结构以及比表面积的影响。采用紫外光降解气相苯测试了合成材料的催化活性。结果表明,以水合肼为氮源合成的N-TiO2表现出最优的光催化活性,其活性明显高于P25,且能够循环使用15次以上。采用气相色谱-质谱技术分析了光降解过程的中间产物,基于此提出了相应的降解机理。
採用三種不同的氮源溶劑熱閤成瞭銳鈦礦-闆鈦礦混晶的N-TiO2催化劑。採用X射線衍射、N2吸附-脫附、X射線光電子能譜和透射電子顯微鏡等手段對催化劑進行瞭錶徵。重點研究瞭不同氮源對催化劑的相組成、晶粒呎吋、微觀結構以及比錶麵積的影響。採用紫外光降解氣相苯測試瞭閤成材料的催化活性。結果錶明,以水閤肼為氮源閤成的N-TiO2錶現齣最優的光催化活性,其活性明顯高于P25,且能夠循環使用15次以上。採用氣相色譜-質譜技術分析瞭光降解過程的中間產物,基于此提齣瞭相應的降解機理。
채용삼충불동적담원용제열합성료예태광-판태광혼정적N-TiO2최화제。채용X사선연사、N2흡부-탈부、X사선광전자능보화투사전자현미경등수단대최화제진행료표정。중점연구료불동담원대최화제적상조성、정립척촌、미관결구이급비표면적적영향。채용자외광강해기상분측시료합성재료적최화활성。결과표명,이수합정위담원합성적N-TiO2표현출최우적광최화활성,기활성명현고우P25,차능구순배사용15차이상。채용기상색보-질보기술분석료광강해과정적중간산물,기우차제출료상응적강해궤리。
Anatase-brookite mixed-phase N-doped TiO2 (N-TiO2) nanoparticles were synthesized through a solvothermal method using different nitrogen sources. The resulting samples were characterized by X-ray diffraction, specific surface area measurement, X-ray photoelectron spectroscopy, and stand-ard and high-resolution transmission electron microscopy. The effects of the different nitrogen sources on phase composition, particle size, microstructure, and specific surface area are investi-gated. The photocatalytic activity of the TiO2 samples was evaluated through photocatalytic degra-dation of gaseous benzene under UV-light irradiation. N-TiO2 prepared using hydrazine hydrate achieved the highest photocatalytic performance in all the samples studied (including the commer-cial P25). Different intermediates during the photocatalytic degradation of benzene over HNT were identified by GC-MS analysis. A detailed reaction mechanism was proposed to explain their for-mation as intermediates in the reaction. Moreover, the photocatalytic activity of the nanoparticles remained almost unchanged after 15 gaseous-benzene degradation test cycles.