催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2011年
7期
1191-1198
,共8页
杂多酸%环戊烯%戊二醛%选择性氧化%SBA-15
雜多痠%環戊烯%戊二醛%選擇性氧化%SBA-15
잡다산%배무희%무이철%선택성양화%SBA-15
heteropolyacid%cyelopentene%glutaraldehyde%selective oxidation%SBA-15
采用离子交换法将Keggin型12-磷钨杂多酸负载到表面胺基化的介孔SBA-15分子筛上,并利用X射线衍射、N2吸附-脱附、傅里叶变换红外光谱、X射线光电子能谱和热重分析等手段对催化剂进行了表征.结果表明,所制备催化剂具有SBA-15分子筛的有序六方孔道结构,负载后的磷钨杂多酸的Keggin结构未遭到破坏,所制备催化剂对以过氧化氢为氧化剂的环戊烯氧化反应具有很高的催化活性,环戊烯转化率可达100%,戊二醛选择性可达81%.催化剂具有较高的稳定性,重复使用5次后,其催化活性没有明显下降.
採用離子交換法將Keggin型12-燐鎢雜多痠負載到錶麵胺基化的介孔SBA-15分子篩上,併利用X射線衍射、N2吸附-脫附、傅裏葉變換紅外光譜、X射線光電子能譜和熱重分析等手段對催化劑進行瞭錶徵.結果錶明,所製備催化劑具有SBA-15分子篩的有序六方孔道結構,負載後的燐鎢雜多痠的Keggin結構未遭到破壞,所製備催化劑對以過氧化氫為氧化劑的環戊烯氧化反應具有很高的催化活性,環戊烯轉化率可達100%,戊二醛選擇性可達81%.催化劑具有較高的穩定性,重複使用5次後,其催化活性沒有明顯下降.
채용리자교환법장Keggin형12-린오잡다산부재도표면알기화적개공SBA-15분자사상,병이용X사선연사、N2흡부-탈부、부리협변환홍외광보、X사선광전자능보화열중분석등수단대최화제진행료표정.결과표명,소제비최화제구유SBA-15분자사적유서륙방공도결구,부재후적린오잡다산적Keggin결구미조도파배,소제비최화제대이과양화경위양화제적배무희양화반응구유흔고적최화활성,배무희전화솔가체100%,무이철선택성가체81%.최화제구유교고적은정성,중복사용5차후,기최화활성몰유명현하강.
Keggin-structtured 12-tungstophosphoric acids were immobilized onto the surface of amine-modified mesoporous sieve SBA-15as onium salts.All the catalyst materials were characterized by X-ray diffraction,N2 physisorption,Fourier transform infrared spectroscopy,thermal gravimetric analysis,and X-ray photoelectron spectroscopy for their structural integrity and physieoehemieal properties.Characterization of the catalysts confirmed an ordered hexagonal mesostrueture for SBA-15 and that the Keggin structure of the heteropolyanions on the amine-modified SBA-15 was preserved.The catalytic activities of the catalysts were evaluated for the liquid-phase oxidation of eyclopentene with 50% hydrogen peroxide as the oxidant in tert-butanol.A 100% conversion of cyclopentene and an 81% selectivity for glutaraldehyde were obtained and these were higher than that for the catalysts prepared by direct impregnation.The stability and reusability of the catalysts were studied and the catalysts could be reused at least five times,which indicates their excellent reusability.The influence of reaction temperature and reaction time was also investigated.In addition,a reaction mechanism was proposed.