简介:对于有机卤代物的电化学还原,银基纳米催化剂显示出优异的催化活性。采用简单的化学还原法制备Ag-Ni纳米颗粒(NPs),并采用X射线衍射、紫外-可见光谱、透射电镜以及能量散射谱等方法对制备的纳米催化剂进行表征。采用循环伏安法、计时电流法以及电化学阻抗谱在有机介质中研究Ag-Ni纳米颗粒对苄氯还原的电催化活性。结果表明:Ni元素的加入可明显减小Ag-Ni纳米颗粒的尺寸,使苄氯的还原峰电位φp正移且增加Ag-Ni纳米颗粒的催化活性。然而,当Ni的含量大于一定值后,Ag-Ni纳米颗粒的催化活性反而降低。同时,对Ag-Ni纳米颗粒的协同催化效应进行探讨。
简介:Thecombinationofdeepwetetchingandamagneto-rheologicalfinishing(MRF)processisinvestigatedtosimultaneouslyimprovelaserdamageresistanceofafused-silicasurfaceat355nm.ThesubsequentlydepositedSiO2coatingsareresearchedtoclarifytheimpactofsubstratefinishingtechnologyonthecoatings.Itisrevealedthatadeepremovalproceedingfromthesinglesideordoublesidehadasignificantimpactonthelaser-induceddamagethreshold(LIDT)ofthefusedsilica,especiallyfortherearsurface.Afterthedeepetching,theMRFprocessthatfolloweddoesnotactuallyincreasetheLIDT,butitdoesamelioratethesurfacequalitieswithoutadditionalLIDTdegradation.Thecombinationguaranteeboththeintegrityofthesurface’sfinishandthelaserdamageresistanceofthefusedsilicaandsubsequentSiO2coatings.
简介:在1,6-己二醇溶剂中,以Ru3(CO)12和Fe3(CO)12为原料,采用低温回流方法合成了Ru-Fe纳米粒子催化剂。利用扫描电镜(SEM)、X射线衍射仪(XRD)和电化学技术表征了催化剂的物理特征和电催化性能.催化剂粉末以六方结构的Rux簇为主相,呈现出高度均匀而聚集的纳米颗粒特征.在0.5mol/LH2SO4溶液中,Ru-Fe催化剂对氧还原反应(ORR)的电催化活性高于Rux,主要归因于d电子从Ru原子到Fe原子的转移过程.
简介:Inthepresentwork,core-shellNi@SiO2catalystswereinvestigatedinordertoevaluatetherelevanceofcatalyticactivityandsurfacestatesofNicoreaswellasNinanoparticlessizetocatalyticpartialoxidationofmethane(POM).ThecatalystswerecharacterizedbyN2adsorption,H2-TPR,XRD,TEMandXPStechniques.Thecatalyticperformanceofthecore-shellcatalystswasfoundtobedependentonthesurfacestatesofcatalyst,whichinfluencedtheformationofproducts.Itwasconsideredthatcarbondioxideformedontheoxidizednickelsites(NiO)andcarbonmonoxideproducedonthereducedsites(Ni).ThesurfacestatesofactivemetalinthedynamicwereinfluencedbothbythesizeofNicoreandtheporosityofsilicashell.However,thecatalyticactivitywouldbedebasedwhenthesizeofNicorewasunderacertainextent,whichcanbeascribedtothefactthecarbondepositionincreasedwiththeincreasingcontentofNiO.TheeffectsofsurfacestatesofNi@SiO2catalystonthecatalyticperformancewerediscussedandthereactionpathwayoverNicoreencapsulatedinsidesilicashellwasproposed.
简介:目的探讨超顺磁性氧化铁纳米颗粒(SPIO)标记滑膜间充质干细胞(SMSC)的可行性及标记前后细胞生物学特性的变化。方法将体外分离培养、纯化及鉴定后的兔膝关节SMSC加入不同浓度的SPIO标记液在37℃二氧化碳培养箱孵育,24h后普鲁士蓝染色和透射电镜下观察标记情况,并比较标记前后SMSC的细胞活性及细胞增殖能力情况。结果SPIO标记后SMSC经普鲁士蓝染色细胞质内可见蓝染颗粒,细胞标记率均达95%以上,且随着标记浓度的增高,细胞质蓝染铁颗粒增多,颜色加深。透射电镜下观察,细胞质及吞饮小泡内可见大量高电子致密度颗粒,呈阳性。在标记液浓度为(12.5~50)μg/ml时,标记后的细胞增殖能力与细胞活力与标记前比较无明显差别;当标记液浓度为100μg/ml以上时,细胞增殖能力与细胞活力受到抑制。结论根据初步研究,一定浓度范围的SPIO标记兔SMSC是安全可行的,为解决SMSC在关节内的示踪问题具有重要意义。
简介:Newvisibletransparent,UVabsorption,andhighinfraredreflectionpropertieshavebeenrealizedbydepositingmultilayerSiO2/ZnO:Al/CeO2-TiO2/SiO2filmsontoglasssubstratesatlowtemperaturebyradiofrequencymagnetronsputtering.OptimumthicknessofSiO2,ZnO:Al(ZAO)andCeO2-TiO2(CTO)filmsweredesignedwiththeaidofthinfilmdesignsoftware.Thedegreeofantireflectioncanbecontrolledbyadjustingthethicknessandrefractiveindex.TheouterSiO2filmcandiminishtheinterferencecoloringandincreasethetransparency;theinnerSiO2filmimprovestheadhesionofthecoatingontheglasssubstrateandpreventsCa2+,Na+intheglasssubstratefromenteringtheZAOfilm.Theaveragetransmittanceinthevisiblelightrangeincreasesbynearly18%-20%,ascomparedtodoublelayerZAO/CTOfilms.Andthefilmsdisplayhighinfraredreflectionrateofabove75%inthewavelengthrangeof10-25μmandgoodUVabsorption(〉98%)properties.Thesesystemsareeasytoproduceonalargescaleatlowcostandexhibithighmechanicalandchemicaldurability.ThetriplefunctionalfilmswithhighUVabsorption,antireflectiveandhighinfraredreflectionratewilladapttoapplicationinflatpaneldisplayandarchitecturalcoatingglass,automotiveglass,withdiminishinglightpollutionaswellasdecreasingeyefatigueandincreasingcomfort.
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:Afacilemethodforthesynthesisofsilver-silica(Ag-SiO2)Janusparticleswithfunctionalitiessuitablefortextileapplicationsisreported.SilicananoparticlespreparedbytheStobermethodwerefunctionalizedwithepoxy,amine,andthiolgroups,whichwereconfirmedbyFouriertransforminfraredanalysis.ThefunctionalizedsilicananoparticleswereusedtoproducePickeringemulsions,andtheexposedsurfacewasusedfortheattachmentofsilvernanoparticles(AgNPs)viathelow-temperaturechemicalreductionmethod.ThemorphologyandstructureoftheAg-SiO2Janusparticleswerecharacterizedbyscanningelectronmicroscopy,scanningtransmissionelectronmicroscopy,high-resolutiontransmissionelectronmicroscopy,energy-dispersiveX-rayanalysis,andUV-visspectroscopy.Becauseoftheirspecificfunctionalities,theseAg-SiO2Janusparticlesareproposedforapplicationsontextilesubstrates,astheycanovercomeseveraldrawbacksofdirectapplicationofAgNPsontextiles,suchasleaching,agglomeration,andinstabilityduringstorage.
简介:Inthiswork,theinfluenceofCO2onthestructuralvariationandcatalyticperformanceofNa2WO4/Mn/SiO2foroxidativecouplingofmethanetoethylenewasinvestigated.ThecatalystwaspreparedbyimpregnationmethodandcharacterizedbyXRD,RamanandXPStechniques.AppropriateamountofCO2inthereactantgasesenhancedtheformationofsurfacetetrahedralNa2WO4speciesandpromotedthemigrationofOinMOx,Na,Wfromthecatalystbulktosurface,whichwerefavorableforoxidativecouplingofmethane.WhenthemolarratioofCH4/O2/CO2was3/1/2,enrichedsurfacetetrahedralNa2WO4speciesandhighsurfaceconcentrationofOinMOx,Na,Wweredetected,andthenhighCH4conversionof33.1%andhighC2H4selectivityof56.2%wereobtained.WithfurtherincreaseofCO2inthereagentgases,thecontentofactivesurfacetetrahedralNa2WO4speciesandsurfaceconcentrationofOinMOx,Na,Wdecreased,whilethatofinactivespecies(MnWO4andMn2O3)increaseddramatically,leadingtolowCH4conversionandlowC2H4selectivity.ItcouldbespeculatedthatNa2WO4crystalwastransformedintoMnWO4crystalwithexcessiveCO2addedunderthereactionconditions.PretreatmentofNa2WO4/Mn/SiO2catalystbymoderateamountofCO2beforeOCMalsopromotedtheformationofNa2WO4species.
简介:Sr1.995–1.5xGdxSiO4:0.005Eu2+phosphorserieswithx=0–0.08molfornear-ultravioletwhitelight-emittingdiodes(NUVw-LEDs)weresynthesizedviasolid-statereactionmethod.XRDprofilepatternandrefinementresultsdemonstratedthatdopingGd3+ionsresultedinthephasetransformation(β-Sr2SiO4→α’-Sr2SiO4).Thephotoluminescencespectrumofthesamplewithx=0moldisplayedtwoemissionpeakscenteredat470and525nm.Thetwo-peakspectrabecameone-peakspectrawiththeGd3+concentrationincreasing.Actually,thefittingresultsdemonstratedthattheone-peakspectrawerestillcomposedoftwosingleemissionspectra.ThephotoluminescenceintensitywasimprovedandtheCIEchromaticitycoordinateswereadjustedviadopingGd3+.
简介:基于炉渣结构分子和离子共存理论,建立1273-1733K下的PbO-CaO-SiO2-FeO-Fe2O3渣系氧化铅活度热力学模型,计算PbO活度并绘制等活度曲线,考察炉渣碱度Q、氧化铁比率R和温度T对活度NPbO和活度系数γPbO的影响。结果表明,活度系数γPbO的模型计算值与文献测定值吻合程度高,说明该模型能较好地反映该渣系结构本质;NPbO呈拉乌尔正偏差,且随渣中PbO含量的升高而增大,但受温度的影响不明显;γPbO随Q的升高而增大;对于Q〉0.3的碱性渣,γPbO随R的升高而出现极大值。该研究结果可用于现代炼铅工艺的热力学研究和操作优化。
简介:以四氯化锡和氨水作为原料,采用水热合成法制备SnO2纳米粉体。探讨反应溶液浓度、水热合成温度、水热合成时间和初始溶液pH值对纳米SnO2粉体性能及形貌的影响规律,并确定最佳工艺参数,同时对水热合成过程中出现的SnO2纳米棒异常现象进行初步分析。结果表明:采用水热合成法制备的SnO2纳米粉体均为四方晶系金红石型结构,粉末粒径为5~12nm,呈近球形。在反应溶液浓度0.5~2.0mol/L条件下,随反应溶液浓度升高,制备的粉体晶粒平均粒径呈线性增长;在水热合成温度160~220℃范围内,随温度升高,SnO2粉体的平均粒径从5.1nm增大到9.8nm,在200℃时会出现降低;在水热合成时间6~30h条件下,随反应时间延长,SnO2粉体的平均粒径增大,在20h时降低;随溶液pH值升高,制备的粉体晶粒平均粒径减小。在1.0mol/L、pH值10的反应溶液中,在200℃保温20h的工艺条件下进行水热合成反应,所制备的粉体平均粒径为5.5~8.5nm,粉体均匀性和分散性良好。
简介:PureAl2O3-2SiO2powderswerepreparedbysol-gelandcoprecipitationmethods,andtheiralkaliactivationreactivitieswerecompared.Thealkali-activationreactivityofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbythecoprecipitationmethod.Thepowderswereinvestigatedby27AIand29Simagic-anglespinningnuclearmagneticresonancespectroscopy(MASNMR)tounderstandtherelationshipbetweentheirstructureandalkali-activationreactivity.The27AlMASNMRdatashowedthatthefive-coordinateAIcontentofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbycoprecipitation.Thehighercontentoffive-coordinateAlcorrespondedtohigheralkali-activationreactivity.The29SiMASNMRdatashowedthatforthepowderpreparedbythesol-gelmethod,siliconwasreplacedbyaluminumatsecondarycoordinationsitesofthecentralSiatomsduringcalcination.However,forthepowderpreparedbysingle-batchcoprecipitation,themainchangewasfromalowdegreeofpolycondensationtoahighdegreeofpolycondensation.