简介:通过溶胶-凝胶法结合光催化还原法制备掺Mo^6+附Ag的TiO2纳米颗粒,并在可见光下对酸性大红3R进行降解实验,研究其在可见光下的催化活性,并与纯TiO2、仅掺Mo^6+或仅附Ag的TiO2进行对比。进一步讨论在可见光照射下掺杂量、焙烧温度等因素对掺Mo^6+附Ag纳米TiO2降解性能的影响。结果表明:可见光下Ag/Mo6+/TiO2比纯TiO2、仅掺Mo6+或仅附Ag的TiO2显示出更高的活性,这是因为金属Mo6+的掺杂和贵金属银的沉积使二氧化钛的吸收带边发生红移,拓宽了可见光的响应范围;Ag/Mo^6+/TiO2催化剂的催化活性最高时的Mo^6+掺杂量为4.5%,银的附着量为2%。焙烧温度为500℃,这种掺Mo6+附Ag纳米TiO2对酸性大红3R的降解率可达87.6%.
简介:ThephaseandmorphologytransformationduringthehydrothermaltreatingprocessofY2O3wasevaluatedwithX-raydiffcrcnce(XRD),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),particlesizeandspecificsurfaceareadetermination.TheresultsshowedthatthecubicY2O3didnottransferintohexagonalY(OH)3inpurewater.Therefore,purehexagonalY(OH)3withnanotubeandmicrorodmorphologieswereobtainedbyhydrothermaltreatingY2O3at150℃for12hin15mlof2mol/LNaOHsolutionwithandwith-outPVAorPEGItwassuggestedthatthecharacteristicpreferentialgrowthofY(OH)3wasattributedtothestructureanisotropyofhexahedronY(OH)3.TheadditionofPVAorPEGcouldpromotetheformingprocessofnanotubesbyselectiveadsorptionondifferentcrystalplanes,whichalteredthegrowthratealongdifferentdirectionsandresultedinthediffusionlimitofconstructingionsinthecentertopofrods.Finally,Y(OH)3:EuandY2O3:Eunanotubeswerealsosynthesizedbyusingthismethod,andtheirphotoluminescencepropertieswereevaluated.
简介:Thesolutionreactionmechanisms,composition,donoratoms,propertiesofcoordinatelinkandstabilityofthecomplexesonthesystemsofadrenalinewithNa3+,Gd3+andTm3+havebeenstudiedbypH-potentiometrictitrationandelectronicspectroscopy.Adrenalineperturbsthef-felectronictransitionofNd3+andTm3+sothattheabsorptionspectraoftheircomplexesareshiftedtowardlongerwavelengths.Theabsorptionspectraofthecomplexesformedbythethreef-blockelementionswithadrenalineareshiftedtowardshorterwavelengthswiththeincreaseofPHinΔγ=350~650nm
简介:Traditionally,austeniticstainlesssteels304and316havebeenemployedincoastalregionsasroofingmaterialsunfortunately,theyareexpensiveandnotfullyresistanttopittingcorrosionunderseverecoastalcorrosiveenvironment.AferriticstainlesssteelB445Rwasdeveloped.Comparedwithaustenitic316L,B445Ris①lesscostly;②uperiorcorrosionresistantwithminormaintenanceforlong-termservice;③insusceptibletothermaldistortionintheweldingseam.B445Rsheetshowsahigheryieldstrengthandlowertensilestrength,lowerelongationandlowerwork-hardeningthanaustenitic316L.Itcanbeeasilyfabricatedanddeformedjustlikeplaincarbonsteel.Afterbending180o,thereisnooccurrenceof'cracking'ornoticeable'orangepeel'.Theformabilityoftheweldingseamisalsosatisfactory.ThepittingpotentialofB445Ris650mV,largerthanthatof304and316L,asshowninFig.1.ThecorrosionrateofB445Rsubmergedin6%FeCl,solutionis0.3-0.56g/(m2?h-1),muchlowerthanthatof316L,asshowninFig.2.ThesuperiorpittingcorrosionresistanceofB445RcanbeascribedtosynergeticeffectofhigherCrandMo.Dull-finishedB445RsheetshavebeenemployedastheroofingmaterialsforGuangzhouAsianGamesArena,asshowninFig.3.About380tof1.0mmB445Rwithdullfinishwasusedforroofingpanels.About100tof0.8mmB445Rwithhairlineorfluororesinpaintfinishwasusedforsidewallpanels.Thecompositeroofbuild-up(fromuptobottom)includes:①shinglesofferriticstainlesssteelB445R;②Kalzip-typestandingseamofaustenitic304;③water-proofDFM;④structuralsteel;⑤75mmthickinsulation;⑥secondarypurlinof150mm×100mm×4.5mmofgalvaniziedQ235;⑦0.8mmthickprofiledeckofgalvaniziedQ235;⑧acousticinsulation.Theroofingshinglesorpanelswiththesamewidthbutdifferentlengthwereformedbybendingfoursidesandfixedtoa'L'shapereinforcingframesofstainlesssteelbyfasteners.The'L'frameswasconnectedtoribsofthestandingseambyacl
简介:YbAl3(BO3)4crystalofgoodopticalqualitywasgrownbythefluxmethod.ThestructureofYbAl3(BO3)4crystalwasdeterminedbysingle-crystalX-raydiffraction.TheexperimentshowsthatYbAl3(BO3)4belongstothedoubleborateswithatrigonalstructure.ThespacegroupisR32anditsunitcellconstantsweremeasuredtobea=0.92965nm,c=0.72129nm,V=0.53673nm3,Z=3.Thetransmittancespectraweremeasured.Thecut-offofYbAl3(BO3)4crystalis216nm,andtherearetwoabsorptionpeakslocatedat940and975nmfrom190nmto2600nm.ThethermalpropertiesofYbAl3(BO3)4crystalwerestudiedforthefirsttime.Theaveragethermalexpansioncoefficientsweredeterminedtobe2×10-6/℃,9.5×10-6/℃alonga-andc-direction.ThespecificheatofYbAl3(BO3)4crystalwasmeasuredtobe0.6695J·(g·℃)-1atroomtemperature.AllresultsindicatethattheYbAl3(BO3)4crystalisanexcellentstoichioimetriclasermaterial.
简介:Er3+-Tm3+-Yb3+tri-dopedBaMoO4phosphorsweresynthesizedbyco-precipitationtechniqueandcharacterizedbyX-raydiffractionanalysis,absorptionstudyandfieldemissionscanningelectronmicroscopyanalysis.Upconversionaswellasdownconversionluminescencestudieswereperformedbyusingnearinfrared(980nm)andultraviolet(380nm)excitations.Energyleveldiagram,pumppowerdependenceandcolourcoordinatestudywereutilizedtodescribethemulticolorupconversionemissionproperties.Undersingle980nmdiodelaserexcitationthedualmodesensingbehaviourisrealizedviaStarksublevelsandthermallycoupledenergylevelsoftheTm3+andEr3+ionsinthepreparedtri-dopedphosphors.AcomparativefluorescenceintensityratioanalysisforintegratedemissionintensitiesarisingfromtheStarksublevels{1G4(a)and1G4(b)}andthermallycoupledenergylevels{2H11/2and4S3/2}oftheTm3+andEr3+ions,respectivelywascarriedoutinthepreparedtri-dopedBaMoO4phosphors.ThemaximumsensitivityforthermallycoupledenergylevelsoftheEr3+andStarksublevelsoftheTm3+ionwasreported.Thedevelopedphosphorscouldbeusefulinthedisplaydevicesandopticalthermometricapplications.
简介:本文采用高温团相反应合成TCaTiO3∶Pr3+红色发光材料、报道了Pr3+激活的CaTiO3的光谱特征及长余辉特性,并与CaS∶Eu的光谱特性及长余辉进行了比较。CaTiO3∶Pr3+将是一种具有广泛用途的新材料
简介:Eu3+activatedSr1–xEuxZrO3(x=0.01–0.04)phosphorwithperovskitestructurewassuccessfullysynthesizedbyusingcombustionmethod.Thestructure,morphologyandopticalpropertiesofthematerialwerecharacterizedbyX-raydiffraction,scanningelectronmicroscopyandfluorescencespectrometry.TheXRDresultsindicatedthatcrystalsofSrZrO3:Eu3+belongstotetragonalperovskitesystem.ThephosphorcouldbeeffectivelyexcitedbyUVlightandtheemissionspectraresultsindicatedthatreddish-orangeluminescenceofSrZrO3:Eu3+duetomagneticdipoletransition5D0→7F1at593nmwasdominant.Thus,thepreparedphosphorshowedremarkableluminescentpropertieswhichfindapplicationsinfieldemissiondisplay(FED)andplasmadisplaypanel(PDP)devices.