简介:InthedischargeofEASTtokamak,itisobservedthat(2,1)neoclassicaltearingmode(NTM)istriggeredbymodecouplingwitha(1,1)internalmode.Usingsingularvaluedecomposition(SVD)methodforsoftX-rayemissionandforelectroncyclotronemission(ECE),thecouplingspatialstructuresandcouplingprocessbetweenthesetwomodesareanalyzedindetail.TheresultsofSVDforECErevealthatthephasedifferencebetweenthesetwomodesequalstozero.Thisisconsistentwiththeperfectcouplingcondition.Finally,performingstatisticalanalysisofγ1/1,ζ1/1andω2/1,wefindthatγ1/1moreaccuratelyrepresentsthecouplingstrengththanζ1/1,andγ1/1isalsostronglyrelatedtothe(2,1)NTMtriggering,whereγ1/1isthewidthof(1,1)internalmode,ζ1/1istheperturbedamplitudeof(1,1)internalmode,andω2/1denotesthemagneticislandwidthof(2,1)NTM.
简介:
简介:StableoperatingregionintheHL-1Mtokamakhasbeenextendedbymeansofwallconditioning,corefuellingandcurrentcontroltechniques.Themechanismsoftheextensionareanalyzedinthispaper.Lithiumizationdiminishestheimpuritiesandhydrogenrecyclingtothelowestlevel.Afterlithiumizationahighdensityupto7×1019m-3wasobtainedeasilybystronggaspuffingwithordinaryohmicdischargealone.MoreattractivelywefoundthatmetalLi-coatingexhibitedtheeffectsofwallstabilization.Thelowqalimitwithhigherdensitywasextendedbyafactorof1.5~2incomparisonwiththatforboronization,and1.2forsiliconization.Siliconizationnotonlyextendedstableoperatingregionsignificantlybyitself,butalsoprovidedagoodtargetplasmaforotherexperimentsofraisingdensitylimit.Corefuellingschemesarefavourableespeciallyforsiliconizedwallwithahigherlevelofmedium-Zimpurity(Z=14).Aftersiliconizationthemaximumdensitynearto1020m-3wasachievedbyacombinationofsupersonicmoleculebeaminjectionandmultipelletinjection.ThenewdefinedslopeofHugilllimitillustratingmoreclearlythesituationunderlowqaandhighnedischargeswascreatedtoindicatethenewregionextendedbycombiningIpramp-upwithcorefuelling.TheslopewithalargeMurakamicoefficientincreasedbyafactorof50~60%.
简介:
简介:本文对合成制备的LiNiO2、LiCo2和LiNixCo1-xO2正极材料以及稀土金属Ce元素添加改性的正极材料进行了XRD和EXAFS表征。结果表明,随着焙烧温度的升高,物相组成趋于单一,晶格趋向完整,800℃时完全形成LiNiO2、LiCoO2晶相结合。LiNiCoO2样品中Ni/Co比不影响LiNiO2晶相的形成,而只影响其晶相组成;掺杂的稀土金属Ce元素以CeO2状态存在于产物中,CeO2对LiNiO2晶相形成有一定的影响;LiCoO2的焙烧温度不能大于900℃,否则Co被氧化为Co3O4;样品中Ni与Co原子的局域结构,除Ni与Co原子相互影响外,掺杂Ce后对它们的局域结构也有较大影响。
简介:利用角分辨紫外光电子谱对乙烯和乙炔气体在Ru(1010)表面的吸附及与K的共吸附的研究结果表明:当衬底温度超过200K,乙烯即发生脱氢反应,σCH和σCC能级均向高结合能方向移动。在室温下,σCH和σCC能级位置与乙炔在Ru(1010)表面的吸附时的分子能级完全一致。乙烯发生脱氢反应后的主要产物为乙炔。衬底温度从120K到室温,Ru(1010)表面上乙炔的σCH和σCC能级均未发现变化。室温下乙炔仍然可以在Ru(1010)表面以分子状态稳定吸附。在有K的Ru(1010)表面上,室温时σCC谱峰几乎。碱金属K的存在促进了乙炔的分解。
简介:SpectroscopicmethodsareusedtoinvestigatecoordinationstructureofN-picolylpolyurethanetransitionmetalcomplexes(PUPYM,M=Co^2+andNi^2+).Geometricalarrangementofligandsinfirst-shellcoordinationsphereofmetalionsispostulatedtobetetrahedralCoL2Cl2andoctahedralNiL2-Cl2Z2.whereListhepicolylgroupandZisahydrate.FromextendedX-rayabsorptionfinestructure(EXAFS)analysis,bondlengthsformetal-chlorineandmetal-ligandofPUPYMaresimilartothoseofsmallmolecularweighttransitionmetalcomplexes.Atwo-phasemodelofPUPYMwhichbestdescribestheexperimentaldataofDMTAandSAXS.isproposed.Onemicrophaseistheharddomainofselfsegregatedhaedsegmentsbroughtaboutbymetal-ligandinteraction.andtheotherphaseisthematrixofsoftsegments.Transitionmetalion-ligandmoietiesandtheirinteractionsdominatethemacroscopicthermalbehaviorofPUPYM.Theligandfieldstabilizationenergydifference(ΔLFSE)betweenmteald-electronsincomplexeswithtwopicolylligandsinthecoordinationsphereofmetalionsandcomplexesmaintainingonepicolylligandascoordinationpendentgroupiscalculatedonthebasisofobservedcoordinationstructure,anditrepresentstheenergysuppliedtosplitcoordinationcross-links.ΔLFSEofpolyurethanenickel(II)complexislargerthanthatofthecobalt(II)complex,Sincethemobilityofhardsegmentsisininverseproportiontothestrengthofcoordinationcross-links.ahigherα-transitiontemperatureofPUPYNi^2+withrespecttoPUPYCo^2+isfoundasexpected.
简介:Surfacemodificationofpolypropylenemicroporousmembrane(PPMM)wasperformedbyatmosphericpressuredielectricbarrierdischargeplasmaimmobilizationofN,Ndimethylaminoethylmethacrylate(DMAEMA).Structuralandmorphologicalchangesonthemembranesurfacewerecharacterizedbyattenuatedtotalreflection-Fouriertransforminfraredspectroscopy(FT-IR/ATR),X-rayphotoelectronspectroscope(XPS)andfieldemissionscanningelectronmicroscopy(FE-SEM).Watercontactanglesofthemembranesurfaceswerealsomeasuredbythesessiledropmethod.Resultsrevealthatboththeplasma-treatingconditionsandtheadsorbedDMAEMAamounthaveremarkableeffectsontheimmobilizationdegreeofDMAEMA.Peroxidedeterminationby1,1-diphenyl-2-picrvlhydrazyl(DPPH)methodverifiestheexsistenceofradicalsinducedbyplasma,whichactivizetheimmobilizationreaction.PurewatercontactangleonthemembranesurfacedecreasedwiththeincreaseofDMAEMAimmobilizationdegree,whichindicatesanenhancedhydrophilicityforthemodifiedmembranes.Theeffectsofimmobilizationdegreesonpurewaterfluxeswerealsomeasured.Itisshownthatpurewaterfluxesfirstincreasedwithimmobilizationdegreeandthendecreased.Finally,permeationofbovineserumalbumin(BSA)andlysozymesolutionweremeasuredtoevaluatetheantifoulingpropertyoftheDMAEMA-modifiedmembranes,fromwhichitisshownthatbothhydrophilicityandelectrostaticrepulsionarebeneficialformembraneantifouling.
简介:Zn_(1-x)Cu_xOthinfilmsweresynthesizedbytheradiofrequency(RF)magnetronsputteringtechniqueusingaZnOtargetcontainingdifferentpiecesofsmallCu-chips.X-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)wereemployedtoanalyzethecrystallineandmicrostructureofthefihn,andX-rayphotoelectronspectroscopy(XPS)wasusedtoestablishthebondingcharacteristicsandoxidationstatesofcopperinsidetheZnOhost.Roomtemperature(RT)ferromagnetismwasobservedintheZn_(1-x)Cu_xOfilmsbyaQuantumDesignsuperconductingquantmninterferencedevice(SQUID)andthesaturationmagneticmomentofthefilmswasfoundtodecreasewiththeincreaseinCucontent.