简介：在n+~(10)B反应，~5He簇排放与更新的水平计划和新光模型被讨论了参数。在这篇论文，与~5He排放有关的反应隧道详细被列出。由为轻原子核使用新反应模型，为n+~(10)的全部的出去的中子的thedouble微分的生气的节在E_n=14.2兆电子伏的B反应被计算了，并且结果与大小相当同意很好。特别地，在精力尖的系列，对全部的出去的中子双differential十字节的从~5He排放的贡献也被分析了，并且在14.2兆电子伏被给了的E_n=的60°的partialenergy尖的系列。一旦~5He排放被考虑，计算结果显示那，有在低精力区域的全部的出去的中子的double-differentialmeasurements的试穿能被改进。因此，在轻原子核的反应过程适当地认为~是5He排放是必要的。

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简介：Inthispaperwepresentanoverviewoftheongoingstudiestobuildupaframeworkthatsupportstheanalysisafterthereprocessingphase.ThisframeworkaimstodevelopastandarddataquerylanguagefortheHEPcommunity,Therelatedstudieshavebeenconsideringtherelationaldatabasemodelaspossibleapproachopposedtotheobjectmodel.SeveraloptimizingandtunningtechniquesarebeingusedintechnologieslikeDB2[3],Oracle[5]andRoot[2],thataresimultaneouslybeingevaluated.TheexperienceobtainedcanbeseenasavaluabletestbedforthefutureLHCandsimultaneouslyasinterestinginputforthedevelopmentoftheGRID.

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简介：采用燃烧法合成了La1.6（MoO_4）_3：Eu_0.4^3＋纳米晶末，研究了其声子一掺杂-晶格相互作用和发光性质。x射线粉末衍射（XRD）分析表明，在500～900℃退火后，La1.6（MoO_4）_3：Eu_0.4^3＋样品为单一晶相。对样品进行了光致发光（PL）测量，激发Mo^6＋-O^2-电荷迁移带，观察到Eu^3＋的系列发光，表明Mo^6＋-O^2-带和Eu^3＋间存在能量传递，中心波长分别在λ1=469nm和λ2=426nm处的两个one-phonon边带，相应的声子能量分别为767和1202cm^-1，分别对应于Mo=0和Mo-0-Mo伸缩振动。同时，计算了两个局域模电子一声子耦合强度的黄昆因子分别为S1=0．055和S2=0．037，为揭示其三价离子高传导特性及其负热膨胀物理特性提供了实验基础。

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简介：ThecorrelationbetweenphasestructuresandsurfaceacidityofAl2O3supportscalcinedatdifferenttemperaturesandthecatalyticperformanceofNi/Al2O3catalystsintheproductionofsyntheticnaturalgas(SNG)viaCOmethanationwassystematicallyinvestigated.Aseriesof10wt%NiO/Al2O3catalystswerepreparedbytheconventionalimpregnationmethod,andthephasestructuresandsurfaceacidityofAl2O3supportswereadjustedbycalciningthecommercialγ-Al2O3atdifferenttemperatures(600–1200C).COmethanationreactionwascarriedoutinthetemperaturerangeof300–600Catdifferentweighthourlyspacevelocities(WHSV=30000and120000mL·g-1h-1)andpressures(0.1and3.0MPa).ItwasfoundthathighcalcinationtemperaturenotonlyledtothegrowthinNiparticlesize,butalsoweakenedtheinteractionbetweenNinanoparticlesandAl2O3supportsduetotherapiddecreaseofthespecificsurfaceareaandacidityofAl2O3supports.Interestingly,NicatalystssupportedonAl2O3calcinedat1200C(Ni/Al2O3-1200)exhibitedthebestcatalyticactivityforCOmethanationunderdifferentreactionconditions.LifetimereactiontestsalsoindicatedthatNi/Al2O3-1200wasthemostactiveandstablecatalystcomparedwiththeotherthreecatalysts,whosesupportswerecalcinedatlowertemperatures(600,800and1000C).ThesefindingswouldthereforebehelpfultodevelopNi/Al2O3methanationcatalystforSNGproduction.

简介：A60%Fe/Al2O3catalystwaspreparedbytheco-precipitationmethod.ItwasreducedbyH2toproducemetallicFe,whichwasthensulfidedbyCS2toFe0.96SandFe3S4orphosphidedbytriphenylphosphine(PPh3)inliquidphasestoFe2PandFeP.Itwasfoundthattheironsulfides(Fe0.96SandFe3S4)exhibitedthelowactivityforthehydrodesulfurization(HDS)reactions.TheHDSactivitywasalsolowontheFe(metal)/Al2O3andFe2P/Al2O3catalystssincetheywereconvertedintoFe0.96SandFe3S4duringtheHDSreactions.Incontrast,theFeP/Al2O3wasfoundtobestableandactivefortheHDSreactions.Inparticular,FeP/Al2O3possessedsignificantlysmallerFePparticlesthanFeP/C,leadingtothesignificanthigherHDSactivityofFeP/Al2O3thanFeP/C.

简介：用多光子光电效应理论简要分析了多光子光电效应实验,指出多光子光电效应满足nhν=12mv20+φ(hν0)且nν/ν0=4/3。同时用微扰法及单光子光电效应理论分析了H原子电离问题,结果表明也是当ω/ω0=4/3时电离几率最大

简介：Theshapeofnanostructurehasimportanteffectsontheirproperties,thereforeinthisstudy,wehavepreparedandcharacterizedthreedifferentmorphologiesofWO3nanostructuresi.e.nanorod,nanosphereandnanoplateforsurveyingshapeeffectontheirphotocatalyticpropertiestowarddegradationofRhodamineB(RhB)dye.ObtainedresultsshowthatnanoplateWO3incomparisonwithothershasthebestphotocatalyticactivity.AccordingtoSEM,andphotocatalyticdegradationresults,thereasonforthisbehavioristhesharpedgesandcornersofWO3nanoplates.Becauseoftheirlowcoordinationnumber,atomslocatedintheedgesandcornersoftheWO3nanoplateshavemoreactivity,adsorbmoreRhBandthereforegivemorephotocatalyticactivitytotheWO3nanoplates.UsingofdifferentscavengersshowedthathydroxylradicalsaremainlyresponsibleforphotocatalyticactivityofWO3nanoplatesandnanospheresbutforWO3nanorods,superoxideradicalsarethemainphotocatalyticdegradationagents.

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简介：Theeffectofpromotercobaltandthesequencesofaddingcobaltandmolybdenumprecursorsontheperformanceofsulfur-resistantmethanationwereinvestigated.AllthesesampleswerepreparedbyimpregnationmethodandcharacterizedbyN2-adsorption,X-raydiffraction(XRD),temperature-programmedreduction(TPR)andlaserRamanspectroscopy(LRS).TheconversionsofCOforMo-Co/Al,Co-Mo/AlandCoMo/Alcatalystswere59.7%,54.3%and53.9%,respectively.Amongthesecatalysts,theMo-Co/AlcatalystpreparedstepwiselybyimpregnatingMoprecursorfirstlyshowedthebestcatalyticperformance.Meanwhile,theconversionsofCOwere48.9%forMo/Alcatalystand10.5%forCo/Alcatalyst.TheadditionofcobaltspeciescouldimprovethecatalyticactivityofMo/Alcatalyst.TheN2-adsorptionresultsshowedthatCo-Mo/Alcatalysthadthesmallestspecificsurfaceareaamongthesecatalysts.CoMoO4speciesinCoMo/AlcatalystweredetectedwithXRD,TPRandLRS.Moreover,crystalMoS2whichwasreportedtobelessactivethanamorphousMoS2wasfoundinbothCo-Mo/AlandCoMo/Alcatalysts.Mo-Co/Alcatalystshowedthebestcatalyticperformanceasithadanappropriatesurfacestructure,i.e.,nocrystalMoS2andverylittleCoMoO4species.