苯催化加氢制备环己烷工艺及催化剂改性分析-preparation of cyclohexane by catalytic hydrogenation of benzene and analysis of catalyst modification.docxVIP
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苯催化加氢制备环己烷工艺及催化剂改性分析-preparation of cyclohexane by catalytic hydrogenation of benzene and analysis of catalyst modification
?勺/Ill一--一一←一一一一一一一本原旦!牛运区I_:J贞g尘豆l监立一-一一一一一一一一一一-催化苯转化率为57.17%,P-Ni/Ti02催化剂为25.10%,Ni在载体表面均匀分散,可显著提高催化剂活性;但过量的磷酸改性,因在载体上生成了NiO结晶体,反而会造成活性的降低。(5)选取P-l%、Ni-lO%的p-Ni/y-^1203催化剂,考察了其制备过程中焰烧温度对活性的影响。实验结果表明:在熔烧温度350-600.C范罔内,450C时的催化苯转化率最佳,可达57.17%。关键词:环己炕,苯,气相催化,磷酸改性,助剂太原理工大学硕士研究生常付论文STUDYONTECHNOLOGYOFBEN乙ENEHYDROGENATIONTOCYCLOHEXANEANDCATALYSTMODIFIEDABSTRACTAsanorganicsolvent,organicrawmaterialandacompositionofthesynthesisprocessofpolyamidefiberproducts,CyclohexanecanbegainedbyBcnzenchydrogenationandoiIfractionsrecovery.WiththerequicmentsofCyclohexaneincreasingrapidly,oilfractionsrecoverycannotafforditinquantityandquality,soBenzenebydrogenationhasbeenthemainmethodtoCyclohexane.Inpacewiththeprogressofrefiningcoalcok.ingproducts,ithasbeenanimportantstudyfìeldforBenzenerefinedformcokingcrudeBenzenetoCyclohexane.Currently,theactivecomponenlinBenzenehydrogenalion.::atalystsismainlynoblemetal.Thecommonmethodofimprovingcatalyticactivityis10increasetheloading,whichleadstoincreaselheconsurnplionofnoblemctalandreducccconomicbenefit.Inorder10rcduceprocesscost,slrengthenproductioncapacityandthereasonableapplicationofnaturalre$ourcesintheficldofcoaJ-cokingrefinedprocess,itisimperativetodcvelopakindofeconomicalandpracticalbenzenehydrogenationcatalystwithlowerloading.-lurV太原理l人学硕士明究生学位i文1nthispaper,thecatalystswerepreparedusingvolumetricimmersionmethodwhichwasusedinbenzenehydrogenationbyintegralcyclohexanereactor.ThepropertieswerecharacterizedbyXRD,TPRandIRetc.TakentheconversionrateandselectivityofCyclohexaneastheevaluationstandardofcatalysts,thebenzenehydrogenationcatalyticprocessandcataly创sofpr巳paratingCyclohexanewerestudi巳dinlh巳?Sp巳ctsofr巳:.1ctlonop巳ratingconditiol1soptimization,supportselectionandadditives,supportandpreparationprocessconditions.Themainconclusionswere:(1)WithNi(N03)2precursor,Ni/y-AI20}(loadingmasspercentis:10%,Ni-30%)catalystwassynthesized.Theeffectofreactiontemperature(T),Hydrogen-?enzenemoleratio(H2/C6H6),Benzeneliquidspacevelocity(VLsp)andreactionpresslIr巳(
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