简介:ThehydrolysisofcephanoneinTritonX-100micelleandTritonX-100/n-C5H11OH/H2O(O/W)microemulsionwerestudiedbymeansofUV-Visabsorptionspectroscopy.Theresultsshowthatcomparedwithwater,TritonX-100micelleandTritonX-100/n-C5H11OH/H2O(O/W)microemulsioncaninhibitthehydrolysisofcephanone.TheinhibitioneffectsofTritonX-100micelleandTritonX-100/n-C5H11OH/H2O(O/W)microemulsiononthehydrolysisofcephanonearerelatedtothelocationofcephanoneintheinterphasesofTritonX-100micellesandTritonX-100/n-C5H11OH/H2O(O/W)microemulsiondroplets.
简介:针对多种类不锈钢多元素成分解析问题,应用X射线荧光光谱分析软件UniQuant,采用扩展基本参数法对多元不锈钢、双相不锈钢进行光谱干扰校正和基体校正,重新设定和优化多元不锈钢基体元素的测试条件,计算背景因子、杂质因子、谱线灵敏度系数和光谱重叠系数,测定Si、Mn、S、P、Ni、Cr、Cu、Mo、V、Al、Ti、Nb、Co、Ta、Fe的相对标准偏差在0.04%-3.8%,Ca、Zr、W、As、Sb、Sn的相对标准偏差在5.4%-20.3%,未知样品检测值与认定值比对结果相当理想,Ni、Cr的平均偏差小于0.05%,可以用很少标准样品实现各类型不锈钢多元素成分准确检测,检测范围宽,适用性好。
简介:在MP2/6-311++G**水平上优化乙烯酮自由基与LiX(X=F,Cl,Br)形成锂键复合物.当卤素的电负性很强(如F元素),使得Li原子处于缺电子状态,此时,电子给体会把电子偏移向锂,形成共价性较强的锂键.而当卤素的电负性减弱时,锂键中主要成分逐渐变为离子键,并且此时锂键性质还要受电子给体影响.另外,由于HCCO为缺电子结构,电负性较弱且体积较大的卤素中的孤对电子会与HCCO之间通过静电相互作用,使得HCCO…Li—X键夹角变小,接近120°.锂键性质对HCCO…LiX(X=F,Cl,Br)复合物中Li—X的伸缩振动频率有直接影响.当锂键表现为共价性时,该频率红移,而当锂键表现为离子性时,该频率蓝移.但是,由于Cl的电负性与O的接近,C的电负性与Br接近所以,在O…Li…Cl和C…Li…Br中容易形成共振结构,导致远大于在其他复合物中的红移.
简介:Wereportthatβ’-Gd2(MoO4)3crystalshavebeengrownbytheCzochralski(CZ)method.Westudiedthegrowthconditionsfoβ’-Gd2(MoO4)3crystal.Acompatisonbetweentheresistance-heatedmethodandradiofrequencyinduction-heatedmethodisdescribed.Also,theinsituobservationofthedomainstructurebythemicroscopeandbysynchrotronradiationX-raytopographyundertheconditionsofDCpolarizationvoltageandtempertaturechangewerecarriedout.Experimentsshowedthatmultidomainstructureincludingferroelectricandferroelasticdomainsoccurredinβ’-Gd2(MoO4)3cystal.Usuallyferroeletiricdomainsappearedintheas-growncrystalandferroelasticdomainsappearedinthepolishedthinnerpiece.BothferroelectricandferroelasticdomainsdisappearedwhenthetemperatureofthecrystalpiecewashigherthantheCurietempperatureTcandtheycouldbereproducedwhenthetemperatureofthecrystalpiecewasloweredbelowTC.WhenaDCpolarizationvoltagerangingfrom150to500Vwasappliedonac-axisβ’-Gd2(MoO4)3piecehavingathicknessof0.5mm,themultidomainwouldgraduallytransformtoasingledomain.Thisresualmeansthatitispossibletomakeaperiodicallypoledβ’-Gd2(MoO4)3crystal.2001ElsevierScienceB.V.Allrightsreserved.
简介:提出了以自制的标准样品,采用单点法绘制校准曲线,利用X射线荧光光谱仪测定FeSiB非晶薄带样品中硅、硼和铁的含量。对于4个FeSiB非晶合金薄带样品中硅、硼和铁进行了10次测定,其分析结果的相对标准偏差分别为0.4%~0.5%、1.3%~4.2%和0.2%~0.4%。方法的分析结果与火花源原子发射光谱法、化学重量法和电感耦合等离子体原子发射光谱(ICP-AES)法的测定值吻合较好。方法快速、简便,薄带样品无需制样,适用于FeSiB非晶合金薄带的快速成分分析。
简介:Si-richsiliconnitridefilmsarepreparedbyplasma-enhancedchemicalvapordepositionmethod,followedbythermalannealingtoformtheSinanocrystals(Si-NCs)embeddedinSiNxfloatinggateMOSstructures.Thecapacitance–voltage(C–V),current–voltage(I–V),andadmittance–voltage(G–V)measurementsareusedtoinvestigatethechargingcharacteristics.Itisfoundthatthemaximumflatbandvoltageshift(△VFB)duetofullchargedholes(~6.2V)ismuchlargerthanthatduetofullchargedelectrons(~1V).ThechargingdisplacementcurrentpeaksofelectronsandholescanbealsoobservedbytheI–Vmeasurements,respectively.FromtheG–VmeasurementswefindthattheholeinjectionisinfluencedbytheoxideholetrapswhicharelocatedneartheSiO2/Si-substrateinterface.CombiningtheresultsofC–VandG–Vmeasurements,wefindthattheholechargingoftheSi-NCsoccursviaatwo-steptunnelingmechanism.TheevolutionofG–VpeakoriginatedfromoxidetrapsexhibitstheprocessofholeinjectionintothesedefectsandtransferringtotheSi-NCs.
简介:Ceriumoxidenanoparticlescoatedbysodiumbis(2-ethylexyl)sulphosuccinate(AOT)werepreparedbyusingamicroemulsionmethod.Transmissionelectronmicroscopyrevealedanaverageparticlesiaeof2-3nm.X-raydiffractionshowedthattheceriumoxidenanoparticlesretaintheCeF2-typecubicstructureslikethebulkcrystal.Theintermediatevalenceofformallytetravalentcompoundshadbeendetectedbyx-ray-absorptionnear-edgestructetravalentcompoundshadbeendetectedbyx-ray-absorptionnear-degestructure(XANES)spectraofCeLIIIabsorptioninbulkCeO2andtheceriumoxidenanoparticles.Twowellresovedwhitelinescanbeassignedtotheelectronconfigurationsof4f^0Land4f^1L,respectively,whereLdenotesaligandhole.Atthesametime,theceriumoxidenanoparticlesalsoshowedthestructuralfeatresoftrivalentcompounds,incomparisontothetrivalentCe(NO3)3·6H2O.FuorLorentzianfunctionsandtwoarctanfunctionswereusedtofitthenormalizedXANESspectra.Theextendedx-ray-absorptionfine-structure(EXAFS)techniquewasusedtoprobethelocalatomicstructuresaroundtheabsorberCe.ThemultielectrornexcitationeffectontheEXAFSspectrawaseliminated.Acor-shellmodelwasusedtodeducethenear-neighbourstructuralparametersaroundcerium.BulkCeO2witheightoxygenatomslocatedat2.343AwasusedasthereferencesampletoextractthebackscatteringamplitudeandphaseshiftoftheCe-Obond.OnehalfoftheatomelocateatthecorepartwiththeCeF2-typecubicstructures(eightoxyensat2.343AaroundCe),theotherhalfoftheatomsareamorphousphaselocatedintheshellpart(surfaceofthenanoparticles)withapproximatelyCe2O3structuralfeatures(averageedsevenoxygensat2.50AaroundCe).
简介:theAlternatingSegmentCrank-Nicolsonschemeforone-dimensionaldiffusionequationhasbeendevelopedin[1],andtheAlternatingBlockCrank-Nicolsonmethodfortwo-dimensionalproblemin[2].Themethodshavetheadvantagesofparallelcomputing,stabilityandgoodaccuracy.Inthispaperforthetwo-dimensionaldiffusionequation,thenetregionisdividedintobands,aspecialkindofblock.ThismethodiscalledthealternatingBandCrank-Nicolsonmethod.
简介:ThecatalyticactivitiesofMnOx-WO3/TiO2forselectivecatalyticreduction(SCR)ofNOwithNH3wereinvestigatedinawiderangeoftemperatureandreactioncondition.ItyieldedaNOxconversionof80.3%-99.6%andaN2productselectivityof100%-98.7%during100°Cto350°Catgashourlyspacevelocity(GHSV)=18900h-1.Inthepresenceof0.01%SO2and6%H2Oat120°C,theNOxconversioncanmaintain98.5%.At300°Candwith0.07%SO2inreactantstream,theNOxconversionstabilizedat99%ashighasthecommercialV-W/TiO2catalyst'slevel.Thesteady-statekineticsstudyshowsthatO2playedapromotingrole.Inthepresenceoflessthan1.5%O2,NOxconversioncanincreasesharplywiththeincreaseofO2concentration.ThereactionorderwaszerowithrespecttoNH3andfirstwithrespecttoNOwithexcessO2andH2O.Thekineticsactiveenergy(Ea)ofMn-W/TiO2wascalculatedtobe6.24kJ/molaccordingtothekineticexperimentatvarioustemperatures,muchlowerthanthoseofothercatalystsreportedintheliterature.Mn-W/TiO2isanexcellentcatalystforSCRofNOwithNH3bynow.
简介:Tonguesquamouscellcarcinoma(ToSCC)isthemostcommontypeofheadandnecksquamouscellcarcinomaandisthesixthleadingcauseofcancerdeathsworldwide[1].Inclinicaloncology,radiationtherapyisastandardtreatmentusedfortumors.Numerousstudieshaveshownthatconventionalradiotherapyusedincancertreatmentmayincreasetheriskofmetastasisofmalignanttumorcells[2–4].Toimprovepatientsurvival,thepotentialformetastasisoftumorsinresponsetoradiationneedstobeaddressed.
简介:二维拉氏自适应流体动力学软件LAD2D,是采用建立在拉氏自适应结构和非结构网格上的有限体积格式,可以计算平面二维和柱对称二维多物质大变形弹塑性流体动力学问题。LAD2D软件系统主要由5部分组成:主控程序、数据模块、前处理模块、主体计算模块、网格模块和后处理模块。其中主体计算采用了结构网格与非结构网格联合使用的拉氏网格体系,计算格式采用了有限体积格式。网格模块包括网格生成、自适应网格加密(AMR技术)和网格重分技术,以及网格改变后物理量守恒重映技术。LAD2D软件系统由主体程序、二维网格生成程序(GRID2D)、二维自适应网格加密程序(AMR2D)、二维自适应程序(ADAPT2D)f[I-维物理量重映程序(REMAP2D)组成。
简介:Self-emissionx-rayshadowgraphyprovidesamethodtomeasuretheablation-fronttrajectoryandlow-modenonuniformityofatargetimplodedbydirectlyilluminatingafusioncapsulewithlaserbeams.Thetechniqueusestime-resolvedimagesofsoftx-rays(>1keV)emittedfromthecoronalplasmaofthetargetimagedontoanx-rayframingcameratodeterminethepositionoftheablationfront.Methodsusedtoaccuratelymeasuretheablation-frontradius(δR=±1.15μm),image-to-imagetiming(δ(t)=±2.5ps)andabsolutetiming(δt=±10ps)arepresented.Angularaveragingoftheimagesprovidesanaverageradiusmeasurementofδ(Rav)=±0.15μmandanerrorinvelocityofδV/V=±3%.ThistechniquewasappliedontheOmegaLaserFacility[Boehlyetal.,Opt.Commun.133,495(1997)]andtheNationalIgnitionFacility[CampbellandHogan,PlasmaPhys.Control.Fusion41,B39(1999)].
简介:Twoseriesofmixedoxides,CoAlMandMgAlM(M=Cr,Mn,Fe,Co,Ni,Cu),werepreparedbycalciningtheircorrespondinghydrotalcite-likecompounds(HTLc).TheratioofMg:Al:M(orCo:Al:M)was3:1:1.ThecatalyticactivityofallsamplesforthereactionofNO+COwasinvestigated.TheresultsshowedthattheactivityofCoAlMwasmuchhigherthanthatofMgAlM.ThestructureandthepropertyofredoxwerecharacterizedbyXRDandH2-TPR.TheresultsindicatedthatonlyMgOphasewasobservedaftercalciningMgAlMhydrotalcites,andthetransitionmetalsbecamemorestable.Thespinel-likephaseappearedinallofCoAlMsamplesafterthecalcination,andthetransitionmetalswerechangedtobemoreactive,andeasilyreduced.TheactivitiesofthreeseriesofmixedoxidesCoAlCuobtainedfromdifferentpreparationmethods,differentratioofCo:Al:Cuandatdifferentcalcinationtemperatures,werestudiedindetailforproposingthemechanismofreaction.TheabilityofadsorptionofNOandCO