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1,4-丁二醇脱氢制γ-丁内酯的研究 Title:StudyontheDehydrogenationof1,4-ButanediolfortheProductionofγ-Butyrolactone Abstract: Thedehydrogenationof1,4-butanediolisapromisingroutefortheproductionofγ-butyrolactone,whichisanimportantchemicalintermediatewidelyusedinthemanufacturingofsolvents,pharmaceuticals,andpolymers.Thisstudyaimstoinvestigatethedehydrogenationprocess,catalysts,reactionconditions,andpotentialapplicationsofγ-butyrolactone.Theresearchfindingsprovidevaluableinsightsintothedevelopmentofanefficientandsustainableprocessforγ-butyrolactoneproduction. Introduction: 1,4-butanediol(BDO)isawidelyavailablecompound,commonlyusedinepoxyresin,polyurethane,andpolyesterproduction.ThedehydrogenationofBDOforthesynthesisofγ-butyrolactone(GBL)offerssignificantadvantagescomparedtotraditionalchemicalroutesduetoitsinherentsimplicityandlowenvironmentalimpact.TheobjectiveofthisstudyistoexplorethevariousaspectsofBDOdehydrogenationforGBLsynthesis. Catalysts: SeveraltypesofcatalystshavebeeninvestigatedforBDOdehydrogenation,includingmetaloxides,supportedcatalysts,andvariousmetalcatalysts.Metaloxides,suchascopperoxide,arecommonlyusedduetotheirhighactivityandselectivitytowardsGBLformation.Supportedcatalysts,suchasplatinumoncarbon,offerimprovedstabilityandselectivity.Othermetals,includingnickel,palladium,andruthenium,havealsoshownpromisingcatalyticactivityinBDOdehydrogenation. ReactionConditions: SeveralreactionvariablesinfluencetheefficiencyandselectivityofBDOdehydrogenation.Thereactiontemperature,catalystloading,reactantconcentration,andgasflowrateplaycriticalrolesindeterminingtheconversionofBDOandtheselectivitytowardsGBL.Higherreactiontemperatures(>300°C)tendtofavorGBLformationbutcanalsoleadtoundesirablesidereactions.OptimalreactionconditionsshouldbedeterminedbasedonthedesiredGBLyieldandselectivity. ReactionMechanisms: ThedehydrogenationofBDOtoGBLinvolvestheremovaloftwohydrogenatoms.Theprimarymechanismproposedisatwo-stepprocess:first,BDOundergoesdehydrogenationtoformbutyraldehyde,followedbyaCannizza

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