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时间:2020-05-20
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1、ChineseJournalofCatalysis36(2015)721-727催化学报2015年第36卷g5期Ivcw~v.chxb.cnavallableatwww.sclencedlrect.com’scienceDirectjourrlaIhorrlepage:www.eIsevier.com/Iocate/chrljcArticleOxidationofsWrenetobenzaldehydebyp-toluenesulfonicacidusinghydrogenperoxideinthepresenceofactivatedca
2、rbonNianzheLi,YuanGao,XinxinZhang,ZhanjunYu,LeiShi,QiSunInstituteofChem&tryforFunctionalizedMaterials,FacultyofChem&tryandChemicalEngineering,LiaoningNormalUniversity,Dalian116029,Liaoninfl,ChinaARTlCLElNF0ABSTRACTArticleh&tory:Theselectiveoxidationofst),renetobenzaldehyde
3、catalyzedbyP—toluenesulfonicacid一TsOH)inReceived25December2014thepresenceofactivatedcarbonfAC)wasinvestigatedwithH202astheoxidant.Thereactionpa·Accepted30January2015rametersofreactiontime,temperature,catalystmass,andstyrene/H202molarratioswereevalu—Published20May2015ated.A
4、strongpromotingeffectofAContheP-TsOH/H202systemwasobserved.TheappropriateratioandamountsofACandP—TsOHwereanimportantfactor.TheaciditvofP-TsOHdoesnotplayasignificantrole.P-TsOHreactedwithH202byanon.radicalprocesstooxidizestyrene.Thefunc.Keywords:StyrenetionoftheACwastoactiv
5、ateH202andtohelptheP-TsOH/H202systeminst),reneoxidation.TheHydrogenperoxidereductionofoxygencontaininggroups(一OH,一COOH)onACbyahightemperaturetreatmentorintroductionof—S03HgroupsontoACaffectedthestvreneconversion.The—S03HgroupswereP—Toluenesulf0nicacidmoreeffectivethantheox
6、ygen—containinggroupsontheACinpromotingstyreneoxidation.A~ivatedcarbon⑥2015.DalianInstituteofChemicalPhysics,ChineseAcademyofSciences.OxidationPublishedbyElsevierB.V.Al1rightsreserved.1.1ntroductionmetal-freeheterogeneouscatalystfortheoxidationofhydro.quinonestothec0rresp0
7、ndjng1,4_benzOquin0neswithH202.TheselectiveoxidationofsrenetobenzaldehydecanbeYangetal-【16】investigatedsulfonatedcarbonasacatalystforcarriedoutbyusingatmosphericoxygen[1,2】,alkylhydroper—theoxidationofaldehydestothecorrespondingacidsbyH202.oxides[3,4】,orH202【5-9】intheprese
8、nceofanappropriateSatoetal_【17】reportedaprocedureforthesynthesisofmetal—basedcatalysttoac
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