負(fù)載型納米Au催化劑上苯酐選擇性加氫制備苯酞的分析

負(fù)載型納米Au催化劑上苯酐選擇性加氫制備苯酞的分析

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時(shí)間:2019-06-25

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1、浙江工業(yè)大學(xué)碩士學(xué)位論文STUDYONSUPPORTEDGOLDNANOCATALYSTSFORSELECTIVEHYDROGENATIONOFPHTHALICANHYDIUDETOPHTHALIDEABSTRACTPhthalideisoneimportantintermediateoffmechemicals,whichisconventionallyusedinpharmaceuticals,pesticidesanddye.Selectivehydrogenationofphthalican

2、hydrideisagreenrouteforphthalidesynthesis.Duringhydrogenationofphthalicanhydride,severalbyproductswillbeobserved.Soit’Snecessarytoexplorecatalystswithhi曲activityandselectivity.Inthisthesis,aseriesofsupportedgoldcatalysts,preparedbydeposition—precipitat

3、ionmethod,werefirstlyusedforphthalicanhydridehydrogenation.Theinfluencesofsupporttype,Auloading,calcinationandreductiontemperatures,promotersandpHvalueonthecatalyticpropertiesofthegoldcatalystsweeinvestigated.Thestabilityandthedeactivationmechanismofth

4、egoldcatalystswerealsostudied.ThecatalystswerecharacterizedbymeansofX—raydiffraction(XRD),nitrogenadsorption—desorption(BET),inductivelycoupledplasma—atomicⅡI浙江工業(yè)大學(xué)碩士學(xué)位論文emissionspectrometry(ICP—AES),transmissionelectronmicroscopy(TE舊,andfouriertransfo

5、rminfraredspectroscopyfiT-m).TheresultsshowthatthegoldcatalystpreparedwithTi02assuppport,2.0wt%ofgoldcontent,and5.0wt%ofFe203promoterexhibitesexcellentcatalyticactivityandselectivityforthehydrogenationofphthalicanhydride.ThesizeofAuparticlesatthesurfac

6、eOverAufI'i02catalystpreparedundertheoptimalpreparationconditionsofpHvalueabout8.10,calcinationtemperture300oC,reductiontemperature200oCandcalcinationtime4h,theconversionofphthalicanhydrideandtheselectivitytophthalideis97.63%and95.24%,respectively,when

7、thereactiontimeiS9h.Fe3+CanexpandthecrystallatticeofTi02andformsitesofcrystaldefects,whichisinfavorofintegrationbetweengoldatomandsupport.Inaddition,existenceofFe3+Canenhancethermalstabilitymechanicalstrengthofporewall.Therefore,additionof5.0wt%promote

8、rironoxideobviouslyimprovestheselectivityandstabilityofAu/Ti02catalystinphthalicanhydridehydrogenationreaction.ThereactionconditionsofphthalicanhydridehydrogenationoverAu/Fe203-Ti02catalystwereoptimizedasfollows:reactiontemperature190oC

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