简介：Duetotheirsize-dependentpropertiesandflexibleprocessingchemistry(Alivisatos,1996),monodispersednanocrystalshaveattractedconsiderableattentionfortheirdistinguishedroleinfundamentalstudiesandtechnicalapplications.AlthoughmuchhasbeenreportedonfabricationofmonodispersedinorganicnanocrystalssuchasFe2O3,CdSe,PbSeandZrO2(Peng&Peng,2002;Zhuetal.,2002;Niederbergeretal.,2002;Pangetal.,2001),littlepublishedonthepreparationofBaSO4nanocrystalsandtheircrystalsizeandmorphologywhichaffecttheirperformanceinapplication.PolymeradditiveswithcomplexfunctionshavebeenusedastemplatestodirectorientednucleationandgrowthofBaSO4(Xiaoetal.,2001;Yuetal.,2002;Summersetal.,2002),asanewclassoffunctionalpolymers,theso-calleddouble-hydrophilicblockcopolymers,designedtocontrolthemorphologyofBaSO4(Colfenetal.,2002),includingtheirnanofiberssynthesizedinAOTmicroemulsion(Li&Mann,2000).ThoughsomuchresearchhasbeendevotedtocontrollingtheBaSO4morphologies,thepresentnotewillreportonthesynthesisofBaSO4nanocrystalswithsizecontrolling.

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简介：Well-dispersedBaSO4nanoparticlesweresynthesizedinthepresenceofsodiumpolyacrylate（PAAS）byasimpleprecipitationmethod,withBaCl2and（NH4）2SO4asreactants.ThedifferentrolesperformedbyPAASinthesynthesisofBaSO4nanoparticleswereinvestigatedusingX-raydiffractometry,Fouriertransforminfraredspectroscopy,andtransmissionelectronmicroscopy.TheresultsindicatethattheassynthesizedBaSO4nanoparticlesweresphereswithanaveragediameterof30nmandthattheirsurfaceswereaffectedbythePAAS.Underatypicalprocedureemployed,PAASreactedwithBaCl2toyieldanintermediate,servingasacontrolreleasingagentandseparatingthenucleationandcrystalgrowthprocessesoftheBaSO4nuclei.DuringformationoftheBaSO4nanospheres,theintermediateslowlydissolvedandreleasedbariumandpolyacrylateions,inhibitingthegrowthandaggregationofnewlyformedBaSO4seedsandresultinginparticlesofnarrowdiameterdistributionandimproveddispersibility.Moreover,thesepolyacrylateionsfurthermodifiedthesurfacesoftheBaSO4nanoparticles.

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简介：Fatiguepropertiesofage-hardenedAlalloy2017-T4underultrasonicloadingfrequency(20kHz)wereinvestigatedandcomparedwiththeresultsunderconventionalloadingofrotatingbending(50Hz).Thegrowthofacrackretardedatabout500μminsurfacelengthunderultrasonicloading,whileatabout20μmunderrotatingbending.Althoughstriationsbeingatypicalfracturemechanismwereobservedunderconventionalloading,mostoffracturesurfacewascoveredwithmanyfacetsunderultrasonicloading.Thesefacetswerealsoobservedunderrotatingbendinginnitrogengas.Thedifferenceingrowthmechanismdependingontheloadingfrequencyandtheretardationofacrackgrowthunderultrasonicloadingmaybecausedbytheenvironmentatthecracktipduetohighcrackgrowthrateunderultrasonicloading.

简介：TheinfluenceofNa2SO4ontheformationofZnOwhiskerswasinvestigatedinthispaper.ZnOwhiskerswithaspectratiosofupto50weresynthesizedbydissolvingε-Zn（OH）2precursorinNaOH/Na2SO4solutionatroomtemperature,followedbyagingoftheresultingsolutionat140℃for6h.Fouriertransforminfraredspectroscopy,Ramanspectroscopy,andX-rayphotoelectronspectroscopyanalysesrevealedthatSO42-ionswereprimarilyadsorbedonthe（100）planeoftheZnOwhiskersviaanouter-spherecomplexconfiguration（O-H…O）,therebypromotingtheone-dimensionalgrowthofZnOwhiskersalongthec-axis.

简介：有从30～80nm的尺寸的Fe3O4nanoparticles被湿milling铁粉末在一家行星的球工厂综合。阶段作文和同样综合的产品的形态学被X光检查衍射(XRD)测量，扫描电子显微镜学(SEM)和传播电子显微镜学(TEM)。NanosizedFe3O4粒子被湿milling准备金属性的铁粉末(?200网孔，99%)在与不锈钢装备的一家行星的球工厂，使用的小瓶与50:1并且以300rpm的旋转速度的ball-to-powder团比率在提取的水下面熨球。在这个方法的铁球的使用在Fe3O4formation起了一个关键作用。现在的技术简单，这个过程是容易的执行。

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简介：Octahedron-likeBaMoO4microcrystalsweresynthesizedbytheco-precipitationmethodatroomtemperatureandprocessedinmicrowave-hydrothermalat413Kfordifferenttimes(from30minto5h).ThesemicrocrystalswereanalyzedbyX-raydiffraction(XRD),field-emissiongunscanningelectronmicroscopy(FEG-SEM)andtransmissionelectronmicroscopy(TEM).XRDpatternsshowedthatthismaterialpresentsatetragonalstructurewithoutthepresenceofdeleteriousphases.FEG-SEMandTEMmicrographsrevealedthattheBaMoO4microcrystalspresentanoctahedron-likemorphologywithagglomeratenatureandpoly-disperseparticlesizedistribution.Thesemicrographsalsoindicatedthatthemicrocrystalsgrowalongthe[001]direction.Theobservedcrystallographicplanesinthesestructuresweremodeledcomputationallyandacrystalgrowthmodelwasproposedinordertoexplainthemorphologicalchangesasafunctionofprocessingtime.

简介：TiO2nanoparticlesweresynthesizedbyahomogeneouscontrolledprecipitationmethodusingindustrialtitaniumsulfate(Ti(SO4)2).TheobtainedpowderswerecharacterizedbyX-raydiffraction(XRD),transmissionelectronmicroscope(TEM),Fouriertransforminfraredspectroscopy(FTIR)andICPplasmaspectrometer.EDTAwasusedascomplexingagenttoimprovethepurityandtheformationofTiO2nanoparticles.Experimentalresultsindicatedthatthehigh-purityTiO2nanoparticleswere20nminmeansizeandnearlymonodispersed.

简介：Liquid-solid(L-S)masstransfercoefficients(Ks)werecharacterizedinagas-liquid-solid(G-L-S)three-phasecountercurrentmagneticallystabilizedbed(MSB)usingamorphousalloySRNA-4asthesolidphase.Effectsofsuperficialliquidvelocity,superficialgasvelocity,magneticfieldstrength,liquidviscosityandsurfacetensionwereinvestigated.ExperimentalresultsindicatedthattheexternalmagneticfieldincreasedKsinthree-phaseMSB,ascomparedtothoseinconventionalG-L-Sfluidizedbeds;thatKsincreasedwithmagneticfieldstrength,superficialgasandliquidvelocitiesanddecreasedwithliquidviscosityandsurfacetension;andthatKsshoweduniformaxialandradialdistributionsexceptforsmallincreasesclosetothewall.DimensionlesscorrelationswereestablishedtoestimateKsoftheG-L-ScountercurrentMSBusingSRNA-4catalyst,withanaverageerrorof3.6%.

简介：Thispaperestablishesanon-linearfiniteelementmodel(NFEM)ofL4-L5lumbarspinalsegmentwithaccuratethree-dimensionalsolidligamentsandintervertebraldisc.Forthepurpose,theintervertebraldiscandsurroundingligamentsaremodeledwithfour-nodalthree-dimensionaltetrahedralelementswithhyper-elasticmaterialproperties.Puremomentof10N·mwithoutpreloadisappliedtotheuppervertebralbodyundertheloadingconditionsoflateralbending,backwardextension,torsion,andforwardfle...