简介:OnOctober18—19,2018,threeR&DachievementsforrealizingtheChinesecontentofcoalchemicalindustry,includingtheDCSsystemforSinopec’slargecoaldeepprocessingproject,themethanolsyngascompressortrain,andthelargewater-cooledandgas-cooledmethanolsynthesisreactors,hadpassedtheappraisalinOrdoscityofInnerMongolia.ItislearnedthatthesethreeprojectsarebeingappliedforthefirsttimeinChina’scoalchemicalindustrytosymbolizenewbreakthroughsintheChinesecontentofmajorequipmentownedbytheSinopecCorp.,whichboastsarangeofindependentintellectualpropertyrightstopushforwardthetechnicaladvancementofnationalindustry.
简介:Nitrobenzene-containingindustrialwastewaterwasdegradedinthepresenceofozonecoupledwithH2O2byhighgravitytechnology.Theeffectofhighgravityfactor,H2O2concentration,pHvalue,liquidflow-rate,andreactiontimeontheefficiencyforremovalofnitrobenzenewasinvestigated.TheexperimentalresultsshowthatthehighgravitytechnologyenhancestheozoneutilizationefficiencywithO3/H2O2showingsynergisticeffect.ThedegradationefficiencyintermsoftheCODremovalrateandnitrobenzeneremovalratereached45.8%and50.4%,respectively,underthefollowingreactionconditions,viz.:ahighgravityfactorof66.54,apHvalueof9,aH2O2/O3molarratioof1:1,aliquidflowrateof140L/h,anozoneconcentrationof40mg/L,aH2O2multipledosingmodeof6mL/h,andareactiontimeof4h.Comparedwiththeperformanceofconventionalstirredaerationmixers,thehighgravitytechnologycouldincreasetheCODandnitrobenzeneremovalraterelatedwiththenitrobenzene-containingwastewaterby22.9%and23.3%,respectively.
简介:Alkylationoftoluenewith2-chloro-2-methylpropane(t-Bu-Cl)tosynthesizepara-tert-butyltoluene(PTBT)wascarriedoutinthepresenceoftriethylaminehydrochloride-aluminumchlorideionicliquidsusedasthecatalyst.TheionicliquidswerepreparedwithdifferentmolarratiosofEt3NHCltoAlCl3,andtheeffectofthemolarratiobetweenAlCl3andEt3NHCl,thereactiontime,thereactiontemperature,theionicliquiddosage,aswellasthemolarratiooftoluenetochloro-2-methylpropaneonthealkylationreactionoftoluenewithchloro-2-methyl-propanewasinvestigated.ThetestresultsshowedthattheacidicionicliquidspreparedwithEt3NHClandAlCl3hadgoodactivityandselectivityforthealkylationreactionoftoluenewithalkylchloridetoproducePTBT.TheoptimalreactionconditionswerespecifiedatanAlCl3toEt3NHClratioof1.6,areactiontemperatureof20℃,amassfractionoftoluenetoionicliquidof10%,andachloro-2-methylpropanetotoluenemolarratioof0.5.Underthesuitablereactionconditions,a98%conversionofchloro-2-methylpropaneandan82.5%selectivityofPTBTwereobtained.Ionicliquidscouldbereused5timeswithitscatalyticactivityunchanged,andtheregeneratedionicliquidscanberecycled.
简介:TheesterificationoflauricacidwithmethanolcouldbeefficientlycatalyzedbyZrOCl2·8H2O,andthisreactionwasstudiedtodevelopagreenmethodforbiodieselproduction.Theinfluencingfactors,suchasamountofcatalyst,reactiontimeandmolarratioofacidtomethanol,wereinvestigated.TheresultsindicatedthattheZrOCl2·8H2Ocatalystshowedhighcatalyticactivity,andgavea97.0%methyllaurateconversionrateunderthefollowingoptimizedconditions,viz.:alauricacid/methanolmolarratioof1:10,acatalystdosageof4%,andareactiondurationof2hatmethanolrefluxingtemperature.Thecatalystcouldbeeasilyrecoveredwhileitsactivitycouldbewellretainedafterthreecycles.TheZrOCl2·8H2Ocatalystalsoexhibitedexcellentcatalyticactivityfortheesterificationofdifferentfreelong-chainfattyacids(includingnonedibleoilswithhighacidvalue)withdifferentshortcarbonchainalcohols.Therefore,theZrOCl2·8H2Ocatalysthasgoodpotentialforthesynthesisofbiodieselfromlow-costfeedstockssuchaswastevegetableoilsandnon-edibleoils.
简介:研究了Pd/Nb2O5—Al2O3催化剂的制备方法及用于丙酮加氢合成MIBK的催化性能。实验结果表明,在反应温度160℃,反应压力4MPa条件下,丙酮单程转化率为40%,MIBK选择性为92%。
简介:Inthisstudy,titaniumdioxidesupportedbymulti-walledcarbonnanotubes(MWCNTs/TiO2)andCr-dopedTiO2supportedbyMWCNTs(MWNTs/Cr-TiO2)weresynthesizedbythesol-gelmethod.Thepreparedsampleswerecharacterizedbytransmissionelectronmicroscopy,X-rayphotoelectronspectroscopy,X-raydiffraction,theBrunauerEmmett-Telleranalysis,andtheRamanspectroscopy.TheoxidationandefficiencyforremovalofSO2inasimulatedfluegaswereinvestigatedexperimentallyinafixed-bedreactor.The15%MWCNTs/Cr-Ti02sampledisplayedexcellentadsorptionproperties,andaSO2removalrateequatingto30.4151mg/gfromthesimulatedfluegascontaining2300μg/gofSO2,8%of02,and5%ofH20wasachievedunderoptimalconditionscoveringatemperatureof333.15K,andaspacevelocityof1275h^-1.TheadsorptionprocesswasenhancedbecauseCrdopingmodifiedtheporestructureandinhibitedthegraingrowthofTiO2.Inaddition,theFreundlichandLangmuirmodelsrevealedthatSO2wasmainlyadsorbedthroughchemicaladsorptiononthesamplesurfaces,andthethermodynamicmodelanalysisindicatedthattheadsorptionwasaspontaneous,exothermic,andentropy-reducingprocess.TheadsorptionkineticsofSO2canbedescribedbythepseudosecond-orderkineticandtheBanghamdynamicsmodels.Thepossiblereactionmechanisminvolvedindesulfurizationprocesswasalsoproposed.