简介：Ca-dopedBaMgAl10O17:Eu2+,Mn2+(BAM)bluephosphorsweresynthesizedbyfluxassistedsolid-statereactionmethodusingCaF2andBaF2asco-flux.GooddispersityandparticlesizehomogenizationofhexagonalpurephaseBAMwereobtainedbysinteringat1400℃.TheeffectsoftheCa2+ionscontentonthestructure,morphologyandphotoluminescencepropertiesofthephosphorswerestudied.TheresultsindicatedthattheincorporationofCacoulddecreasethelatticeconstant,improvethehomogeneityanddispersityandenhancethephotoluminescence(PL)intensityofthephosphoreffectively.TheoptimumBa0.86Ca0.04Mg0.97Al10O17:0.1Eu2+,0.03Mn2+PLintensitywasenhancedforabout30%andrelativebrightnesswasimprovedabout4%.Furthermore,thesynthesizedBAMandcommercialBAMphosphorswereannealedfor30minat600oCinair.TheCa-dopedphosphorshadstrongeremissionintensity,higherbrightnessandbetterchromaticitystabilitythanthatofthecommercialphosphor.TheseresultsindicatedthatCa-dopedbluephosphorshadgoodpotentialapplicationsinthecommercialtricolorfluorescentlampsaswellasinotherdisplayandlamps.
简介：SinglephaseofBa1-xMgAl10O17:xEu2+(0.02≤x≤0.14)phosphorswasfirstsuccessfullypreparedbyco-precipitationinaqueousmediumwitha'reversestrike'method,usingoxalicacidandammoniatogetherasprecipitants.Completelycrystallizedphosphorswereobtainedat1300℃,whichis300℃lowerthanthetemperatureofsolid-statereaction.TheirphotoluminescencewasinvestigatedunderUVandVUVregion,respectively.TheemissionspectraofBa1-xMgAl10O17:xEu2+samplesexcitedby254or147nmshowedacharacteristicwidebandwiththepeakcentredatabout450～454nm.Optimumemissionintensityreachedatx=0.1andthenconcentrationquenchingoccurred.Thesynthesizedphosphorshows10%higheremissionintensitythanthatpreparedbysolid-statereaction.
简介：TheeffectsofUVAphotoirradiatedCe(Ⅳ)dopedTiO2nanoparticle(CDTP)onratcoloncarcinomacellline(C26)growth,cellcycledistribution,andmorphologywerestudiedbyMTTassay,FlowCytometry,andfluorescentstaining.Theresultsindicatethatabout64.6%cellsarekilledafter24hby180μg·ml-1CDTPwhen8minexposedtoUVA,over90%deadfor30mingroup,relativeto18.7%,41.5%ofTiO2atthesameconditionrespectively.Hoe33258stainingofthefixedcellsrevealstypicalapoptoticstructures(apoptoticbodies),andcellsarearrestedinG0/G1phase.
简介：ThereactionofNdCl3withlithiummethylnaphthalenein1:2moleratioinTHFgeneratesblackpowder.Thepowderreactswithcyclooctatetraene（COT）inTHFtoformthetitlecomplex.[Li（THF）4Nd（C8H8）2]·2THFcrystallizesinthemonoclinicspacegroupP2/cwithunit-celldimensionsa=1.7858（7）nm,h=1.3243（4）nm,c=1.8086（6）nm.β=106.52（4）°,V=4.10nm3andDc=1.268g/cm3forZ=4.F（000）=1660,R=0.0774,Rn=0.0733.Thecomplexconsistsofdiscreteion-pairandtwoTHFmoleculesadduct.Intheanion,theneodymiumatomiscoordinatedbytwoCOTrings.ThestructureofthecationshowsthatthelithiumatomisattachedwithTHFmoleculesonly.
简介：Heterogeneousprecipitationmethodwasusedtopreparedsurfacecoatingonself-madeBaMgAl10O17:Euphosphor.Resultsillustratethatthecoatingfilmcanbesilicondioxideinamorphousstatewith50nminthickness.Photoluminescenceresultsindicatethatthecoatinglayerpresentsanobservableimprovedeffectontheenhancementofthermalstability.Whenbakedat600℃for1h,theluminanceofcoatedBAMkeepsat92%higherthanthatofuncoatedBAMby23%.ThisprotectiveeffectcanbeattributedtothehighcompactdegreeanduniformityofthisamorphousSiO2coatingfilmwhichisservedasadiffusionblocklayertoinbreakoxygenatom,thusreleasestheoxidationextentofEu2+effectively.
简介：Loadedonthecordierite,therareearthdopedcompositecatalystwaspreparedbysol-gelmethodcombinedwithdippingtechnique.TakingOrthodichlorobenzeneasmodel,thecatalystwasusedtoremovethedioxinsofthewastegas.Theresultsshowedthatat280℃andgasspacevelocitybeing8000h-1,theorthodichlorobenzenecouldberemovedeffectivilybythepreparedCeO2-TiO2-V2O5compositecatalystwhoseactivitywasremarkablyenhancedbythedopingofCe,whiletheindustrialside-streamtestofdioxinsfromrefuseincinerationsmokeindicatedthatthedecompositionratecouldreachabove93%underthesameconditions.
简介：Inthiswork,boththethermalexpansionandelectricalconductivityofnanocrystallineLa2Mo2O9werestudied.ThenanocrystallinepowderofLa2Mo2O9wasobtainedbysol-gelmethod,andwiththehelpofSHP(superhighpressure)upto4.5×104atmat700℃forashorttime,andthenanocrystallinepowderwasdensifiedwithoutobviousparticlesizegrowth.TheelectricalconductivityofnanocrystallineLa2Mo2O9wasoneorderofmagnitudelowerthanthatofthemicrocrystallinesampleatthesametemperature.Owingtothephasetransition,themicrocrystallineLa2Mo2O9hasanabruptincreaseofthermalexpansionwithapeakvalueof48×10-6K-1at556℃.Forthenanocrystallinematerial,thepeakvalueincreasesto112×10-6K-1at520℃.Ontheotherhand,above600℃thesignificantgrowthofparticlesizeofthenanocrystallineLa2Mo2O9wasobserved,accompanyingbyatremendousincreaseofthermalexpansionwithapeakvalueofthirdhigherthanthatofLa2Mo2O9.
简介：Basedonthethermodynamicallyself-consistentanalysisandoptimizationofthreesub-binarysystemsoftheternarysystemPrCl3-CaCl2-MgCl2,thethermodynamicsofthisternarysystemhasbeenstudied.UsingHillertmodelandtakingMgCl2asanasymmetriccomponent,thePrCl3-CaCl2-MgCl2phasediagramhasbeencalculated.Theagreementbetweencalculatedandmeasuredcompositionsandtemperaturesatdeflectingpointsonliquidusisgood.Thesystemisasimpleeutecticonewithaeutecticpointat26.0mol%PrCl3,41.5mol%CaCl2,32.5mol%MgCl2;560℃（calculated）and26.0mol%PrCl3,39.4mol%CaCl2,34.6mol%MgCl2;546℃（measured）,respectively.
简介：TheZrO2-Al2O3ceramiccompositeswerepreparedbyappropriatetechniqueswithcommercialZrO2andAl2O3powdersasrawmaterialsandY2O3asstabilizer.TheresultsindicatethatwiththeintroductionofAl2O3intotheZrO2matrixwherethequantityofadditiveY2O3is3.5%(molefraction),thegrowthofZrO2grainsisefficientlyinhibited,whichhelpstheZrO2grainsexistinametastabletetragonalmanner;thushigherstrengthandtoughnessareacquired.Whenthecontentofaluminais20%(massfraction),thebendingstrengthandfracturetoughnessofthecompositesare676.7MPaand10MPa·m1/2respectively,themechanicalbehaviorsareclosetothosepreparedwithZrO2andAl2O3powderssynthesizedthroughwetchemicalapproach.Themechanicalbehaviorsofthecompositesarewellimprovedowingtothedispersiontougheningofaluminagrainsandphasetransformationtougheningofzirconiagrains.
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：FluorescencespectraofSm2+andEu2+→Sm2+energytransferwerestudiedinSrB4O7.Thereappearsonlyfluorescencefrom5D0transitionofSm2+at77K.Thevibroniclinesassociatedwith5D0→7F0transitionwereobserved.Thethermalpopulationtoupperstatesof5D1and4f5dlevelsfrom5D0givesriseto5D1→7FJand5d→4fradiativetransitionsofSin2+athighertemperature.
简介：Reactionof(MeC5H4)3LnwithHOCH2CH2NMe2intetrahydrofuran(THF)givesthenewcomplexes[(MeC5H4)2Ln(μ-OCH2CH2NMe2)]2(Ln=Sm,Y,Nd)withnitrogenfunctionalizedμ-alkoxideligand.ThecomplexeswerecharacterizedbyelementalanalysisandIR,and[(MeC5H4)2Sm(μ-OCH2CH2NMe2)]2wasstructurallycharacterizedbytheX-raydiffractiontobeadimerformedbytwounsymmetricoxygenbridges.ThecomplexhasatricyclicskeletonwiththeadditionaltwoSm-NbondsviaintramolecularcoordinationofOCH2CH2NMe2.ThecoordinationnumberofthecentralmetalSmisnine.Thetitlecomplexesshowgoodcatalyticactivityforring-openingpolymerizationofε-caprolactone.
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![Synthesis and Crystal Structure of a Novel Ion-pair Complex of [Li（THF）4Nd（<b style='color:red'>C</b>8H8）<b style='color:red'>2</b>]·<b style='color:red'>2</b>THF](/image/thesis5 "Synthesis and Crystal Structure of a Novel Ion-pair Complex of [Li（THF）4Nd（<b style='color:red'>C</b>8H8）<b style='color:red'>2</b>]·<b style='color:red'>2</b>THF")
![Synthesis, Crystal Structure of [ （MeC5H4）<b style='color:red'>2</b>Ln（μ-OCH<b style='color:red'>2</b> CH<b style='color:red'>2</b>NMe<b style='color:red'>2</b> ） ]<b style='color:red'>2</b> （Ln = Sm, Y, Nd） and Their Catalytic Activity for Ring-Opening Polymerization of ε-Caprolactone](/image/thesis18 "Synthesis, Crystal Structure of [ （MeC5H4）<b style='color:red'>2</b>Ln（μ-OCH<b style='color:red'>2</b> CH<b style='color:red'>2</b>NMe<b style='color:red'>2</b> ） ]<b style='color:red'>2</b> （Ln = Sm, Y, Nd） and Their Catalytic Activity for Ring-Opening Polymerization of ε-Caprolactone")
