简介：用常规的浸渍-还原法制备Pt／C催化剂，如果条件控制不好，制备出的Pt粒子大小和分散度不均，且易出现团聚。文中的主要目的是用微波密闭加热的方法，研究制备条件对Pt粒子大小的影响，制备高分散度且Pt粒径大小在一定范围内可控的Pt／C催化剂。

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简介：TheeffectofacidcomponentincludingvariousconventionalacidsandtungsticcompoundsonglucosehydrogenationoveraseriesofbinarycatalystsystemcontainingRu/Ccatalystwasinvestigated.TheresultsshowedthatHCl,H2SO4,H3BO3,H3PO4,andHNO3hadnegligibleeffect,whileallthetungsticcompoundsimposedinhibitingeffectsonthehydrogenationofglucoseoverRu/Ccatalyst,andthesuppressingeffectfollowedtheorderofH2WO4>HPW>WO3>AMT>HSiW.Thisorderisthesameastheorderofethyleneglycol(EG)yieldsintheone-potconversionofglucosetoEG,suggestingtheimportantroleofcompetitionbetweenglucosehydrogenationandretro-aldolcondensationincontrollingtheselectivityofEG.

简介：Thedevelopmentofthehydrogenelectrodeisvitalfortheapplicationofalkalinepolymerelectrolytefuelcells(APEFCs).Inthisstudy,aseriesofNi(OH)2decoratedNi/Ccatalysts(Ni(OH)2-Ni/C)werepreparedbyathree-stepelectrochemicaltreatmentofNi/C.TheexistenceofNi(OH)2wasdemonstratedbyX-rayphotoelectronspectroscopy(XPS),andthesurfacemolarratioofNi(OH)2/Niofthesampleswasestimatedviaanelectrochemicalmethod.TheHORcatalyticactivityofthecatalystswasevaluatedbyarotationdiskelectrode(RDE)method,anda'volcanoplot'wasestablishedbetweentheHORexchangecurrent(j0)andthesurfacemolarratioofNi(OH)2/Ni.Ontopofthe'volcano',thesurfacemolarratioofNi(OH)2/Niis1.1:1,thej0ofwhichwas6.8timesofthatofNi/C.ThestabilityofthesamplestowardHORwasevaluatedtobegood.OurstudyaddedasystematicexperimentalevidencetotheHORresearch,showingthattheHORcatalyticactivityofNicanbedeliberatelycontrolledviadecorationofNi(OH)2,whichmayhelpunderstandingtheHORmechanismonNi.

简介：Twocompactandintense2.45GHzpermanentprotonsourcesandtheircorrespondinglowenergybeamtransport(LEBT)systemsweredevelopedsuccessfullyforChinaAcceleratorDrivenSub-criticalsystem(C-ADS)in2014,oneofwhichwasbuiltatIMP,LanzhouandtheotheratIHEP,Beijing.Bothprotonsourcescandeliverstable10mA/35keVprotonbeamsatCWmodetotheentrancesofthedownstreamRFQs.AsshowninFig.1,thebeamsextractedbya3-electrodeextractionsystemaretransportedbytheLEBTsystem,whichiscomposedof2identicalsolenoids,andintothe3.2or2.1MeVradio-frequencyquadrupole(RFQ).Inordertoensuresuperconductingcavitiescommissioningandprotection,anelectrostatic-chopperhasbeendesignedandinstalledintheLEBTlinethatcanchopthecwbeamFig.2Totalhydrogenionbeamcurrentversusinputpower.intoapulsedone.Theachievedfall/risetimeofthechopperislessthan20ns.

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简介：Catalyticcombustionofpropane-airmixturewasinvestigated.Platinumcatalystsoveraflatstainlesssteelwithγ-aluminawashcoatwereemployed.Theemployedburnerhasthreecatalystssetparalleltothemixtureflow,spacedatanintervalof5,10and15mm.Bothexperimentandnumericalsimulationweremadeatinlettemperatureof553K,inletvelocityof3to7m/sandequivalenceratioof0.3to0.5.Inthenumericalsimulation,two-dimensional,steadystatemodelwasdevelopedtocalculatethetemperatureandspeciesconcentrationingas-phase.Inthismodel.chemicalreactiononthecatalystsurfaceandthatinthegasphasewereassumedtooccurinthree-steps.Thenumericalresultsshowgoodagreementwithexperimentalresults.Itwasfoundthatthepropertiesofthecatalyststronglyaffectthecatalystsurfacetemperature.Especially,thethermalconductivityofcatalysthasagreateffect,whiletheemissivityofcatalysthaslesseffect.

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简介：APt-MoO3/Ccatalyst,aimedtoeliminatetheharmfuleffectofsulfurdioxide（SCb）ontheperformanceofPtnanoparticles（NPs）forcatalysisofoxygenreductionreaction（ORR）inprotonexchangemembranefuelcells（PEMFC）,isdevelopedandcharacterizedbyTEM,XRDandXPS.TheresultsrevealthatPt-MoO3/Ccatalystexhibitsnotonlyahighercatalyticactivity,butalsoabetterSO2poisoningresistanceandabetterrecoveryperformancethanthecommercialPt/Ccatalystdoes.

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简介：现有的C语言教学虽注重了实际能力的培养,但未能注意到学科间的差异。结合电子信息类课程的特点,本文探索了面向专业能力培养的C语言层次化教学改革方向,提出了教学改革的四个重点：教学内容层次化,教学方法层次化,教学评价体系层次化和教学过程层次化,深化学生对C语言课程与专业能力培养之间的认识,提高C语言的教学质量。

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简介：PtRu/SnO2/Ccatalystwaspreparedinapolyolprocess,followedbyreductiontreatmentandalkalineetching.X-raydiffraction,transmissionelectronmicroscopewithenergydispersivespectrometerandXrayphotoelectronspectroscopywereusedtocharacterizethemorphology,structureandcompositionofthecatalysts.COandmethanolelectro-oxidationactivitiesofthecatalystswereevaluatedbyCOstrippingvoltammetry,cyclicvoltammetryandchronoamperometrymeasurements.ReductiontreatmentofthepreparedPtRuSnO2/CcatalystinapolyolprocessinducedtheenrichmentofSnonthesurface,inhibitingmethanoldissolutionandCOadsorptiononPt.AlkalineetchingremovedSnorSnOxandthusexposedPtRuonthesurface,resultinginenhancedactivitiesforCOandmethanolelectro-oxidationduetothesynergyeffectsofPtRuonthesurfaceandSnspeciesbeneath.