简介:Ni-Ti形状记忆合金由于有特殊的形状记忆效应和良好的机械性能成为受到很大关注的功能材料。尽管Ti-Ni合金已经被研究了很多年,至今,仍然有很多有趣的现象并没有得到很好的认识,尤其Ni-Ti合金在不同温度下的应力应变曲线的因素的研究上还有很多没有解释清楚的问题。为此笔者在文中详细介绍了Ni-Ti形状记忆合金的应力与应变关系实验的准备,实验过程,以及实验结果的获取。并对实验结果进行了分析总结,得出Ni-Ti形状记忆合金在不同应力及应变速度下的特性数据,为形状记忆合金的应用提供了必要的参考。
简介:ThetransportpropertieswerestudiedforrareearthmanganeseoxideLa0.67Cao.33Mn1-xFexO3(x=0-O.3)systems.ItisfoundthatwithincreasingFe^3+-dopingcontentx,theresistanceincreasesandtheinsulator-metaltransitiontemperature(T1M)shiftstolowertemperature.Ifthedopingcontentissmall,thetransportpropertiesmanifestmetalliccharacteristicsinthetemperaturerangeofT<T1M,whiletheywillobeyathermalactivationmodelinthetemperaturerangeofT>T1M.SuchabehaviormaybeattributedtotheFe^3+-dopingandpossibleMnionsscatteringtoelectrons.TheFe^3+dopingmayleadtotheformationofFe^3+-O^2--Mn^4+channels,whichcouldterminatethedoubleexchangeMn^3+-O^2--Mn^4+channels.TheantiferromagneticclustersofFeionsmayinducetheMnionstoscettertotheelectrons.
简介:Thephasesandmagnetocaloriceffectinthealloys(Gd1-xErx)5Si1.8Ge2.2withx=0,0.1,0.2and0.3wereinvestigatedbyX-raydiffractionanalysisandmagnetizationmeasurement.ThesamplesweresinglephasewiththemonoclinicGd5Si2Ge2-typestructure.WiththeincreaseofErcontent,theCurietemperature(Tc)decreasedobviouslyfrom253Kofthealloywithx=0to114Kwithx=0.3.Themaximummagneticentropychangedinthesamplesof(Gd1-xErx)5Si1.8Ge2.2withx=0.0,0.1,0.2and0.3were6.88,8.32,9.59and10.24J·kg-1·K-1respectivelyintheappliedfieldchangeof0~2.0T.
简介:ToimprovethemechanicalpropertiesofWC-Al2O3composites,theeffectsoftraceamountofCeO2additivesonthemicrostructureandmechanicalpropertiesoftheWC-Al2O3compositespreparedbyhotpressingwereinvestigated.TheresultsrevealedthattheWC-Al2O3compositesdopedwith0.1%CeO2possessedrefinedmicrostructureandenhancedmechanicalpropertiescomparedwiththatoftheundopedWC-Al2O3composites.TraceCeO2suppressedthedecarburizationofWC,promotedthemicrostructuralrefinement,andimprovedtheinterfacecoherenceoftheWCmatrixandAl2O3.When0.1%CeO2wasaddedtotheWC-Al2O3composites,theeffectofCeO2resultedintheachievementofarelativedensityof98.82%withanexcellentVickershardnessof16.89GPa,combiningafracturetoughnessof9.85MPa·m1/2withanacceptableflexuralstrengthof1024.05MPa.
简介:ThemorphologyandcorrosionbehaviorofNi/Al2O3compositecoatingspreparedusingdouble-pulsedelectrodepositingtechniqueafteroxidizedunder800℃NaCldepositinairenvironmentwereanalyzedbyscanningelectricalmicroscope(SEM),X-raydiffraction(XRD)andenergydispersivespectrum(EDS).TheresultsshowedthatthecorrosionofallcompositecoatingswasacceleratedunderNaCldeposits,andthecorrosionproductswereratherporouswithpooradherencetothematrix.Al2O3particlesinthecoatingscanrefinethegrainsizeandimprovethehightemperaturecorrosionresistanceofthecoatings.Withinthetestscope,themoreAl2O3particlesinthecoatings,thelowercorrosionratescouldbeobtained,andthecorrosionmechanismwasalsodiscussed.
简介:研究不同碳源下Al2O3-SiC-C铁钩料的性能。分别以球沥青、焦炭和炭黑为碳源,比较了常温下三者的显气孔率、抗折和抗压强度。结果表明,不同种类碳源将对试样的气孔率和抗折强度产生不同程度的影响。
简介:AseriesofCe-Fe-Zr-O(x)/MgO(xdenotesthemassfractionofCe-Fe-Zr-O,x=10%,15%,20%,25%,30%)complexoxideoxygencarriersforselectiveoxidationofmethanetosynthesisgaswerepreparedbytheco-precipitationmethod.ThecatalystswerecharacterizedbymeansofX-raydiffractionandH2-TPR.TheXRDmeasurementsshowedthatMgFeO4particleswereformedandFe2O3particleswelldispersedontheoxygencarriers.Thereactionsbetweenmethanedilutedbyargon(10%CH4)andoxygencarrierswereinvestigated.SuitablecontentofCeO2/Fe2O3/ZrO2mixedoxidescouldpromotethereactionbetweenmethaneandoxygencarriers.Therearemainlytwokindsofoxygenofcarriers:surfacelatticeoxygenwhichhadhigheractivitybutlowerselectivity,andbulklatticeoxygenwhichhadloweractivitybuthigherselectivity.Amongallthecatalysts,Ce-Fe-Zr-O(20%)/MgOexhibitedthebestcatalyticperformance.Theconversionofthemethanewasabove56%,andtheselectivityoftheH2andCOwerebothabove93%,theratioofH2/COwasstableandapproachedto2foralongtime.
简介:ThephotocatalystsK4Nb6017andK4Nb6017dopedwithFe^3+andCr^3+werepreparedbysolidstatereactionandwerecharacterizedbypowderx-raydiffraction,UV-visdiffusivereflectanceandscanningelectronmicroscopy.ThephotocatalyticactivityofK4Nb6O17andK4Nb6O17dopedwithFe^3+,Cr^3+wereinvestigatedwithmethanolaselectrondonorandPtaspromotercatalystunder+400nmUVirradiation.Thedifferenceofphotocatalyticactivitybetweenthemwasalsodiscussed.TheindividualrateofhydrogenevolutionfortheK4Nb6O17,Fe-K4Nb6O17andCr-K4Nb6O17asphotocatalystsare5.35,5.00,6.25mmol·L^-1.h^-1respectively.
简介:ThecompoundSm0.98Fe9.02–xGaxNδ(x=0,0.25,0.5,0.75,1)werepreparedbymelt-spunmethodandsubsequentannealingandnitriding.TheRietveldanalysisshowedthatthelatticeexpansionplayedanimportantroleinimprovingtheCurietemperature.AnobviousdevelopmentoftheCurietemperaturewasobtainedwiththeincreasedGacontentfromx=0–1(ΔTc=90oC).Theoptimumcoercivityofnitrideswasobtainedatx=0.25withthevalueHcj=652kA/m(8.15kOe)afterannealing,whichcorrespondedtoareasonabledistributionofgrainsizesofbothTbCu7-typeSmFe9Nδandα-Fe.However,anexcessofGadopingmightleadtoanabnormalgrowthofα-Fe,whichinturndeterioratedthemagneticproperties.ItwasconcludedthatamoderateGacontentwasveryeffectiveinraisingthecoercivityandCurietemperamentintheTbCu7-typeSm-Fe-N.
简介:试图为高温度的熔融的盐反应堆的安装和电极的建设开发材料,在750和950湩爠晥湩浥湥?瑳敲杮桴湥湩?猠汯摩猠汯瑵潩?瑳敲杮桴湥湩?眠牯?慨摲湥湩?愠摮瀠敲楣楰慴楴湯猠牴湥瑧敨楮杮的Ni-11Fe-10Cu的高温度的氧化行为上的艾尔和Y的效果
简介:Phosphine(PH3)isahighlytoxicairpollutant,commonlyproducedinphosphorouschemicalindustry.Butithasreceivedlessresearchattentionduetoitshandlingdifficultly.COisthemaincontentofthephosphorouschemicalindustrytailgas,theconcentrationofwhichisalwaysmorethan80vol.%,anditcanbethefeedgastoproducevariousvaluableproductssuchasformate,oxalate,andmethanolandsoon.But,PH3isoneoftheimportantbarriers,whichisharmfultothefollowingchemicalprocess.Inordertomakeuseofthetailgas,PH3shouldberemovedfirstly,andCOshouldbecoveredinthewholepurifiedprocedureatthesametime.Inthiswork,themodifiedactivatedcarbon(MAC)wasusedastheadsorbenttoseparatePH3fromthemixturetailgas.SeriesofMACadsorbentswerepreparedfortheadsorptionofPH3,whichloadedCu-FeandCe(La),orseparately.ThePH3adsorptioncapacities,chemicalandphysicalpropertiesofMACwereallinvestigated.Theresultsshowedthatover99%PH3adsorptionefficiencywasachievedwhenusedMACadsorbents.TheremovalefficiencyandPH3adsorptioncapacityoftheCu-Fe-Ce/AC(20:1:0.4)werebothmuchhigherthanthosemodifiedactivatedcarbons.ThemaximumPH3adsorptioncapacitywas71mgofPH3/gofMAContheCu-Fe-Ce/AC,whichweremuchhigherthanliteraturedatausingCuOonlyforadsorbinghydridegases.
简介:ThestructureandhydridingperformanceofLa0.6Nd0.4Ni4.8Mn0.2Cux(x=0~0.4)alloyswereinvestigatedinordertodevelopsuitablematerialsformetalhydrideairconditioner.TheeffectofCuadditiononthecrystalstructure,equilibriumpressure,hydrogencapacityandhysteresisaswellashydrogenabsorption/desorptionkineticsweresystematicallystudiedbyusingthemeasurementofP-Cisotherms,X-raydiffractionandscanningelectronmicroscopy.AstheamountofCuincreases,theplateaupressureincreasesandhydrogenabsorption/desorptionkineticsisimproved,buttheeffectivehydrogenstoragecapacitydecreases.Itisshownthatvariationsinthebasalplaneparameteracanbeusedasanindicationfortheplateaupressurechanges.Withtheincreaseofparametera,theplateaupressuredecreases.ForLa0.6Nd0.4Ni4.8Mn0.2Cux(x=0~0.4)alloysthereisarelationshipbetweentheeffectivehydrogenstoragecapacitiesandtheratiosoftheirunitcellparameterscanda.Theeffectivehydrogenstoragecapacitydecreaseswithincreaseofa/c.