简介:Inthisstudy,theweldingthermalcyclecurveexhibitedtwotemperaturepeaksinhighheat-inputtwin-wireseparate-poolsubmerged-arcweldingandcoarse-grainedheataffectedzoneexistedintheweldedjoint.Theinclusionsofprimaryweldmetalandcoarse-grainedheataffectedzoneofCe-addedSAWshouldbeAl203,MnO,Si02,TiO,Ce2S3,CeS,Ce202SandCe203.Undertheeffectofweldingthermalcycle,oxy-sulfidesinclusionsofCe,thediameterofwhichwaslessthan2.0|Jim,slightlygrewlarger,butthecompositionandtypeoftheinclusionsdidn,tchange.ThemicrostructureofthelargeheatinputweldmetalhadacicularferritethatCeoxidesulphideparticlesinducednucleationandproeutectoidferrite.Inthecoarse-grainedheataffectedzoneofweldmetal,home-positionprecipitationofacicularferriteandsympatheticacicularferritewerebothobserved.Itwassupposedthatpreviouscrystalcellsofacicularferriteinaustenitegrainpromotedhome-positionprecipitationofacicularferrite.Meanwhile,sympatheticacicularferritetendedtonucleateattheprimaryacicularferritegrainboundaries,wherehighdislocationdensitywaslocated,andgrewinsidetheneighboringcarbon-depletedausteniticregions.Thegranularbainitenucleatedintheausteniticzonewithhighcarboncontentclosetoacicularferriteandsympatheticacicularferrite.
简介:Nb-24Ti-18Si-2Al-2Hf-4CrandNb-24Ti-18Si-2Al-2Hf-8Cralloyswerepreparedbyarcmeltinginawater-cooledcrucibleunderargonatmosphere.Microstructuralcharacteristicsandoxidationresistanceofthealloysat1250℃wereinvestigated.Theresultsshowthat,whentheCrcontentis4at%,themicrostructuresconsistof(Nb,Ti)_(ss)andNb_5Si_3;asCrcontentincreasesto8at%,C14LavesphaseCr_2Nbisformed.Theisothermaloxidationtestsshowthattheoxidationkineticsofthetwoalloysfollowsimilarfeatures.Theweightgainsofthetwoalloysafteroxidationat1250℃for100hare235.61and198.50mg·cm~(-2),respectively.Duringoxidation,SiO_2,TiO_2,Nb_2O_5andCrNbO_4areformedatfirst.Then,Ti_2Nb_(10)O_(29)isformedafteroxidationfor20minandbeginstochangeintoTiNb_2O_7astheoxidationproceeds.SiO_2isformedassolidstateatfirstbutlaterevolvesintoglassystatetoimprovethecohesionofthescale.Afteroxidationfor100h,oxidationproductsconsistofSiO_2,TiNb_2O_7,Nb_2O_5andCrNbO_4.
简介:ThedosimetricphosphorsLi_3PO_4:M(M=Tb,Cu)wereproducedbymodifiedsolid-statemethod.ThestructuralandmorphologicalcharacterizationwascarriedoutthroughX-raydiffraction(XRD)andscanningelectronmicroscope(SEM).Additionally,thephotoluminescence(PL),thermoluminescence(TL)andopticallystimulatedluminescence(OSL)propertiesofpowderLi_3PO_4dopedwithTbandCuwerestudied.ItisadvocatedthatLi_3PO_4:CuphosphornotonlyshowshigherOSLsensitivity(25timesormore)butalsogivesfasterdecayinOSLsignalsthanthatofLi_3PO_4:Tb~(3+)phosphor.Theminimumdetectabledose(MDD)ofLi_3PO_4:M(M=Tb,Cu)phosphorsisfoundtobe21.69×10~(-3)and3.33×10~(-6)J·kg~(-1),respectively.InOSLmode,phosphorshowslineardoseresponseintherangeof0.02-20.00J·kg~(-1).InTLmode,sensitivityofLi_3PO_4:CuphosphorismorethanthatofLi_3PO_4:Tbphosphor.Thekineticsparameterssuchasactivationenergyandfrequencyfactorsweredeterminedbypeakshapemethod,andphotoionizationcrosssectionsofpreparedphosphorwerecalculated.
简介:ThehotdeformationbehaviorofextrudedAZ80magnesiumalloywasinvestigatedusingcompressiontestsinthetemperaturerangeof250-400℃andstrainraterangeof0.001-1.000s^-1.The3Dpowerdissipationmapwasdevelopedtoevaluatethehotdeformationmechanismsanddeterminetheoptimalprocessingparameters.Twodomainsofdynamicrecrystallizationwereidentifiedfromthe3Dpowerdissipationmap,
简介:TheHAZmicrostructureandperformanceofQuenchingandTemperingmodetemperbeadweldingandgeneralweldedjointswhichweremadeonSA508-3steelof60mmthicknesswerecomparedinthisarticle.Theresultshowsthattemperingsorbitewhichhasexcellentoverallperformancewasobtainedinbothmodes.ThemicrostructureofQuenchingandTemperingmodeweldedjointsgotmorefinegrain.Eventhoughthehardnessoftemperingbeadweldedjointsishigherthanthegeneralone,itstillmeetsthestandardswhichislowerthan350HV.TheimpactabsorbingenergyofeachdistrictoftemperingbeadweldedjointsHAZreached170J,whichisequaltogeneralone.
简介:InordertoimprovethehydrogenstoragepropertiesofLiBH_4-MgH_2composite,twodifferentkindsofNb-basedcatalysts,NbCandNbF_5,wereaddedtoLiBH_4-MgH_2compositebyballmilling,andtheeffectofcatalystsonhydrogenstoragepropertiesofthemodifiedLiBH_4-MgH_2systemwasinvestigated.TheexperimentalresultsshowthatLiBH_4-MgH_2compositeisatwo-stepdehydrogenationprocess,andNb-basedcompoundscanremarkablyenhanceitsdehydrogenationkinetics.Forthecompositewithoutadditionofcatalysts,thestartingdecompositiontemperatureforthefirstdehydrogenationstepisaround320℃,andthereisalongperiodofincubationtime(around220min)fortheoccurrenceoftheseconddecompositionstepevenathightemperatureof450℃.Itneedsmorethan10htocompletethedecompositionprocessandreleasearound9wt%H_2.Afteradditionof5mol%NbF_5,thestartingdecompositiontemperatureforthefirstdehydrogenationstepisaround150℃,thereisnoincubationtimefortheseconddecompositionstep,andittakesaround40mintocompletethesecondstepandreachesatotaldehydrogenationcapacityof9.5wt%.NbF_5hasbettercatalyticeffectthanNbC.Basedonthehydrogenation/dehydrogenationbehaviorsandstructuralvariation,themechanismofcatalyticeffectwasdiscussed.
简介:GrainboundarydiffusiontechniquewithTbH_3nanoparticleswasappliedtofabricateTb-lesssinteredNdFe-Bpermanentmagnetswithhighcoercivity.Themagneticpropertiesandmicrostructureofmagnetsweresystematicallystudied.Thecoercivityandremanenceofgrainboundarydiffusionmagnetareimprovedby112%andreducedby26%comparedwiththoseoftheoriginalmagnet,respectively.Meanwhile,boththeremanencetemperaturecoefficient(α)andthecoercivitytemperaturecoefficient(β)ofthemagnetsareimprovedafterdiffusiontreatment.MicrostructureshowsthatTbelementenrichesinthesurfaceregionofNd_2Fe_(14)Bgrainsandisexpectedtoexistas(Nd,Tb)_2Fe_(14)Bphase.Thus,themagneto-crystallineanisotropyfieldofthemagnetimprovesremarkably.Asaresult,thesinteredNd-FeBmagnetsbygrainboundarydiffusionwithTbH_3nanoparticlesexhibitenhancedcoercivity.
简介:Reducingthemanufacturingcostofsolarcellsisnecessarytotheirindustrialproduction.Electrodepositingisaneffective,non-vacuummethodwhichisverysuitableforcuttingthemanufacturingcostofthinfilmsaswellasdevelopingitslarge-scaleindustrialproduction.Inthisstudy,about1-μm-thickCu(In,Ga)Se_2(CIGS)precursorswereelectrodepositedonMo/glasssubstratesinaqueoussolutionutilizingathree-electrodepotentiostaticsystem.Triethanolaminewasusedascomplexingagent,andallparametersofelectrodepositionwerepreciselycontrolled.Afterthat,theelectrodepositedprecursorswereselenizedinaSeatmospherewithdifferentheatingramprates(60and600℃·min~(-1)).High-qualityCIGSfilmswereobtained,andtheircharacteristicswereinvestigatedbyX-rayfluorescence,scanningelectronmicroscopy,energydispersivespectroscopy,X-raydiffraction,Ramanspectraandnear-infrared-visible(NIR-Vis)spectra.Theresultsrevealthattherearemanydifferencesbetweenthepropertiesofthefilmsunderdifferentheatingrates.Finally,CIGSsolarcellswerefabricatedusingafastandaslowheatingrate.Themaximumefficienciesachievedforthefilmsselenizedat60and600℃-min~(-1)are3.15%and0.71%,respectively.
简介:TheeffectofAl-3Ti-0.2C-5Sr(wt%)grainrefinerontherefiningperformanceandmodificationofA356alloywasinvestigatedusingopticalmicroscope(OM).ThemorphologyandcrystalstructureofternaryAl-Ti-SrphasesinAl-3Ti-0.2C-5Srrefinerwereanalyzedbyscanningelectronmicroscopy(SEM)andtransmissionelectronmicroscopy(TEM).TheresultsshowthattheternaryAl-TiSrphasesinAl-3Ti-0.2C-5SrrefinercanpromotethegrainrefiningefficiencyofA356alloy.TheternaryAl-Ti-Srphasesco-existintwomorphologies,i.e.,blocky-likephaseandsurround-likephase,besides,whichbothhavethesamechemicalcompositionofAl_(34)Ti_3Sr.ThecrystalstructureofAl_(34)Ti_3Srisface-centeredcubic,andthelatticeparameterisdeterminedtobeabout1.52nm.