简介:摘要在固定床反应器上研究了经铈促进的(Ce-promoted)和未经铈促进的5Co-15Ni/Al2O3,催化剂在CH4干法转化反应中的性能。虽然添加铈(2.5wt%)能够明显减少积碳,降幅可达50%,但CH4的反应速度并没有出现明显的提高(增幅小于5%),活化能也没有出现明显的改变。经铈促进的催化剂抗碳(carbonresistance)能力提高,这要归因于反应过程中铈离子稳定的多次氧化态(multipleoxidationstates)。所采用的催化剂的TPR-TPO揭示了两种类型的碳成分(carbonspecies)。第一种是活性Cα,它易于被H2气化,而且还参与氧化铈的氧化还原反应;第二种是相对的非活性Cβ,它只能被O2移除,而且不参与氧化还原反应循环。文中还提出了这种反应的双中心(dual-site)兰格缪尔(Langmuir)-Hinshelwood机理。
简介:Inthiswork,theinfluenceofCO2onthestructuralvariationandcatalyticperformanceofNa2WO4/Mn/SiO2foroxidativecouplingofmethanetoethylenewasinvestigated.ThecatalystwaspreparedbyimpregnationmethodandcharacterizedbyXRD,RamanandXPStechniques.AppropriateamountofCO2inthereactantgasesenhancedtheformationofsurfacetetrahedralNa2WO4speciesandpromotedthemigrationofOinMOx,Na,Wfromthecatalystbulktosurface,whichwerefavorableforoxidativecouplingofmethane.WhenthemolarratioofCH4/O2/CO2was3/1/2,enrichedsurfacetetrahedralNa2WO4speciesandhighsurfaceconcentrationofOinMOx,Na,Wweredetected,andthenhighCH4conversionof33.1%andhighC2H4selectivityof56.2%wereobtained.WithfurtherincreaseofCO2inthereagentgases,thecontentofactivesurfacetetrahedralNa2WO4speciesandsurfaceconcentrationofOinMOx,Na,Wdecreased,whilethatofinactivespecies(MnWO4andMn2O3)increaseddramatically,leadingtolowCH4conversionandlowC2H4selectivity.ItcouldbespeculatedthatNa2WO4crystalwastransformedintoMnWO4crystalwithexcessiveCO2addedunderthereactionconditions.PretreatmentofNa2WO4/Mn/SiO2catalystbymoderateamountofCO2beforeOCMalsopromotedtheformationofNa2WO4species.
简介:本文阐述了Co-Mo系宽温耐硫变换催化剂升温硫化的机理、硫化剂的选取以及采用循环硫化法的具体升温硫化过程。指出该流程中存在的问题,并提出了改进建议。
简介:Newvisibletransparent,UVabsorption,andhighinfraredreflectionpropertieshavebeenrealizedbydepositingmultilayerSiO2/ZnO:Al/CeO2-TiO2/SiO2filmsontoglasssubstratesatlowtemperaturebyradiofrequencymagnetronsputtering.OptimumthicknessofSiO2,ZnO:Al(ZAO)andCeO2-TiO2(CTO)filmsweredesignedwiththeaidofthinfilmdesignsoftware.Thedegreeofantireflectioncanbecontrolledbyadjustingthethicknessandrefractiveindex.TheouterSiO2filmcandiminishtheinterferencecoloringandincreasethetransparency;theinnerSiO2filmimprovestheadhesionofthecoatingontheglasssubstrateandpreventsCa2+,Na+intheglasssubstratefromenteringtheZAOfilm.Theaveragetransmittanceinthevisiblelightrangeincreasesbynearly18%-20%,ascomparedtodoublelayerZAO/CTOfilms.Andthefilmsdisplayhighinfraredreflectionrateofabove75%inthewavelengthrangeof10-25μmandgoodUVabsorption(〉98%)properties.Thesesystemsareeasytoproduceonalargescaleatlowcostandexhibithighmechanicalandchemicaldurability.ThetriplefunctionalfilmswithhighUVabsorption,antireflectiveandhighinfraredreflectionratewilladapttoapplicationinflatpaneldisplayandarchitecturalcoatingglass,automotiveglass,withdiminishinglightpollutionaswellasdecreasingeyefatigueandincreasingcomfort.
简介:摘要采用溶胶-凝胶法制备了Al2O3-ZrO2复合溶胶膜,研究了化学组成和添加剂对复合溶胶的影响。结果表明,当Al2O3/ZrO2=1,DMF=40vol%时,可得到澄清透明,粘度适中,稳定性好,且凝胶干燥后几乎无开裂的溶胶膜
简介:Differentrareearth(RE)ionsdopantswereaddedintotheSrAl2SiO7:Eu2+phosphorsinordertoenhancethephosphorescenceproperties,andtheeffectoftheREionsincludingYb3+,Ce3+,Nd3+,Dy3+andTm3+,wascomparativelyinvestigated.ItwasfoundthatNd3+additionimprovedthephosphorescencepropertiesobviouslyamongallthestudiedREions.Therefore,Sr1.96–xAl2SiO7:xEu2+,yNd3+phosphorswerestudiedindetail,andtheoptimumEu2+andNd3+concentrationsweredeterminedwiththeafterglowtimeofabout20min.Thephasestructures,photoluminescence(PL)properties,long-lastingphosphorescence(LLP)properties,afterglowdecaycurvesandthermo-luminescence(TL)fortheselectedphosphorsduringthecorrespondingstudywereinvestigated.AllthephosphorsexhibitedgreenPLemissionandLLPemission.ThereweretwoTLbandslocatedatabout325and380Kforthestudiedsamples,andtherelationshipbetweenREadditionandphosphorescencepropertieswasdiscussed.
简介:Zirconiagraphiterefractoryisusedasacore-nozzleinthethin-stripcastingofsteel.Post-mortemanalysisofusedrefractorywasperformedinanefforttoestablishthefailuremechanism.CorrosionbehaviorwasstudiedagainstmoltensteelwithMnO-SiO2basedliquidinclusions.CorrosionofthesematerialsinvolvesdissolutionandoxidationofgraphiteinthematrixfollowedbypenetrationofliquidslagleadingtodegradationofZrO2particles.Thermodynamicequilibriumcalculationswereperformedtostudythiscorrosionmechanism.
简介:CO2methanationhasbeenahottopicbecauseofitsimportantapplicationinthespacecraftandpotentialutilizationofcarbondioxide.Nickelcatalystisactiveforthisreaction.However,itsactivitystillneedstobeimproved.Dielectricbarrierdischarge(DBD)plasma,initiatedatambientconditionandoperatedat~150°C,hasbeenemployedinthisworkfordecompositionofnickelprecursortoprepareNi/MgAl2O4.Theplasmadecompositionresultsinhighdispersion,uniquestructure,enhancedreducibilityofNiparticlesandpromotedcatalyst-supportinteraction.AnimprovedactivityofCO2methanationwithahigheryieldofmethanehasbeenachievedovertheplasmadecomposedcatalyst,comparedtothecatalystpreparedthermally.Forexample,themethaneyieldoftheplasmapreparedcatalystis71.8%at300°Cbutitis62.9%overthethermalpreparedcatalyst.ThecatalystcharacterizationconfirmedthatCO2methanationovertheDBDplasmapreparedcatalystfollowspathwayofCOmethanation.