简介：采用溶胶-凝胶法制备纳米级SiO2粉，分别用X射线衍射仪、透射电子显微镜、红外光谱仪和差热扫描量热分析仪对其进行了分析测试。结果表明于凝胶在1200℃热处理1小时仍是无定型的SiO2粉，其平均粒度大小为40nm。

简介：TheapproachofutilizingcombustionsynthesistomakefineparticlesofSiO2,Al2O3andTiO2isaquitemoderntechnology.Throughthechemicalreactioninpost-flameregion,fineSiO2particlescanbeformedwithhighpurityonplatesurface.Therefore,thecombustionsynthesisofSiO2powdersisanimportantareaforfurtherresearchanddevelopment,especiallyfortheapplicationofSiO2inthesemiconductorindustry.Thisinvestigationproposesanexperimentalapproach(i.e.,agas-phasecombustionsynthesis)usingtwodifferentkindsoforganiccompounds,Hexamethyldisilazane(HMDSA)andHexamethyldisioxane(HMDSO),asthesiliconprecursors.ApremixedgasburnerischosenwithC3H8asfuel,airasoxidantandpartoftheairwasusedasthecarryinggastoentrainHMDSA/HMDSOvaporintothecombustiblemixture.ObservationsshowthattheC3H8/airflamechangedcolorfromapale-blueflametolightyellowandthenorangewhendifferentamountsofprecursorswereintroduced.Throughthechemicalreactioninthepost-flameregion,fineSiO2particleswereformedinthegasphaseandthenquenchedandcollectedonanaluminumflatplate.TheobjectiveofthispaperistostudytheeffectsofHMDSOandHMDSAconcentrationsandflametemperaturesonthesynthesisofSiO2particles.

简介：Thioglycolicacid(TGA)-stabilizedCdTenanocrystals(NCs)werepreparedwithsodiumtelluriteastelluriumsource,whichavoidsthecumbersomeprocessesassociatedwithH2TeorNaHTesources.FluorescentCdTe/SiO2compositesweresynthesizedbyasol-gelmethodwithouttheexchangeofsurfaceligands.ThephasestructureofCdTeNCswasinvestigatedbyX-raydiffractometry.Forcomparison,somecharacterizationsweredoneforboththeCdTeNCsandthecomposites.CdTeNCsandCdTe/SiO2compositeswerecharacterizedwithTEM,digitalcameraandfluorescencespectrophotometer.ThestabilityofCdTeNCsandthecompositeswereinvestigatedinphosphate-bufferedsaline(PBS)bufferandthefluorescentpropertiesofthecompositeswerediscussedindetail.

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简介：在通常用于合成中孔ＭＣＭ－４１分子筛的反应体系中，用氨水、ＮａＯＨ或四乙基氢氧化胺作催化剂，在较低的ｐＨ值下合成出具有独特Ｎ２吸附等温线和狭窄双峰中孔分布的双中孔ＳｉＯ２材料。实验表明，在所使用的反应体系中，双中孔ＳｉＯ２结构是一种必然的物相，且反应体系的ｐＨ值调节在合成中起决定性作用。当反应体系的ｐＨ值从约９．５增加到１１时，相应产物的孔径分布由双中孔转变为单中孔分布。这些结果为进一步深入理解中孔材料的形成机理提供了新的视野。合成样品用ＸＲＤ和Ｎ２吸附等温线进行了表征。更多还原

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简介：Anewmethodforfabricatingorderedporoussiliconisreported.Atwo-dimensionalsilicananospherearrayisusedasatemplatewithahydrofluoricacid-hydrogenperoxidesolutionforetchingthenanospheres.Theinitialdiameteranddistributionoftheholesintheresultingporoussiliconlayeraredeterminedbythesizeanddistributionofthesilicananospheres.Thecorrosiontimecanbeusedtocontrolthedepthsoftheholes.ItisfoundthatthepresenceofaSiO_2layer,formedbytheoxidationoftheroughinternalsurfaceofthehole,istheprimaryreasonallowingthecorrosiontoproceed.Ultravioletreflectionandthermalconductivitymeasurementsshowthatthediameteranddistributionoftheholeshaveagreatinfluenceonpropertiesoftheporoussilicon.

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简介：Ahighlyeffcientandgeneralmethodforthesynthesisofpolyfunctionalized4H-pyransisestablishedthroughaone-potmulticomponentcyclocondensationofaromaticaldehydeswithCHacids,malononitrileandethylacetoacetateusingnanosilicasupportedtin(II)chlorideasacatalyst.InthismethodSnCl2/nanoSiO2wasusedasgreenandreusablecatalyst.Excellentyields,shortreactiontimes,simpleworkup,andinexpensivenessandcommerciallyavailabilityofthecatalystaretheadvantagesofthismethod.

简介：HighlyactiveandselectiveCu/SiO2catalystsforhydrogenationofdimethyloxalate(DMO)toethyleneglycol(EG)weresuccessfullypreparedbymeansofaconvenientone-potsyntheticmethodwithtetraethoxysilane(TEOS)asthesourceofsilica.XRD,H2-TPR,SEM,TEM,XRFandN2physisorptionmeasurementswereperformedtocharacterizethetextureandstructureofCu/SiO2catalystswithdifferentcopperloadings.TheactivecomponentswerehighlydispersedonSiO2supports.Furthermore,thecoexistenceofCu0andCu+contributedalottotheexcellentperformanceofCu-TEOScatalysts.TheDMOconversionreached100%andtheEGselectivityreached95%at498Kand2MPawithahighliquidhourlyspacevelocityoverthe27-Cu-TEOScatalystwithanactualcopperloadingof19.0%(massfraction).

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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.

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简介：在相同的反应体系中当ｐｈ值从约９．５调变至１１时分别合成出双中孔ＳｉＯ２和六方中孔ＳｉＯ２材料，并用ＸＲＤ、Ｎ２吸附、ＴＥＭ、ＴＧ／ＤＴＡ和ＦＴＩＲ等测试手段对合成产物进行了表征。实验结果表明，双中孔ＳｉＯ和六方中孔ＳｉＯ２是合成中必然出现的两种不同的中孔物相。与六方中孔ＳｉＯ２相比，双中孔ＳｉＯ２也具有典型中孔材料的特征ＸＲＤ谱图，虽然仅呈现一个易让人产生不完全晶化误解的相对较宽的单ＸＲＤ衍射峰（ｄ＝５．２ｎｍ），但它却给出一种独特的Ｎ２吸附等温线和窄的双峰中孔孔径分布曲线。由于孔壁的无定形及表面活性剂分子与ＳｉＯ２骨架间相似的相互作用，两类材料给出类似的ＦＴＩＲ谱图和ＴＧ／ＤＴＡ曲线。然而，在双中孔ＳｉＯ２的ＦＴＩＲ谱图中９６０ｃｍ处峰强度的微小变化可能意味着在锻烧脱除模板剂后双中孔ＳｉＯ２较六方中孔ＳｉＯ２具有更高的骨架聚合度。更多还原

简介：AseriesofTiO2-XSiO2[Xdenotesthemolarfraction(%)ofsilicainthemixedoxides]withdifferentn(Ti)/n(Si)ratioswaspreparedwithammoniawaterasahydrolysiscatalyst.ThephotocatalystspreparedwerecharacterizedbyXRD,thermalanalysis,FTIR,UV-VisandSPS.ThecharacterizationresultsofFTIRandUV-VisspectrashowthatTiatomsweregraduallychangedfromoctahedralcoordinationtotetrahedralcoordinationwiththeadditionofsilica,whichisnotbeneficialforobtainingstrongBrnstedacidityandhigherphotocatalyticactivity.Thephotocatalyticactivityexperiments,whichwereconductedbyusingheptane(orSO2)asthemodelreactant,showedthatTiO2-SiO2containingasuitableamountofsilicacanexhibitmuchhigherphotocatalyticactivitythanpureTiO2.Theenhancedphotocatalyticactivitycanbeattributedtothreefollowingfactors:(1)smallercrystallinesize;(2)higherthermalstability;(3)thenewstrongBrnstedacidity.

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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.