简介:TheeffectofrapidsolidificationonstructureandelectrochemicalperformanceoftheLaNi4.5Co0.25Al0.25hydrogenstoragealloywasinvestigatedbyX-raypowderdiffractionandasimulatedbatterytest,includingmaximumcapacity,cyclingstability,self-discharge,andhigh-ratedischargeability(HRD).Allthemelt-spunalloysweresingle-phasewiththeCaCu5-typestructure(spacegroupP6/mmm).Incomparisontotheas-castalloy,therapidlyquenchedalloysmanifestedanimprovedhomogeneityofcompositionandexpandedlatticeparameters.Theelectrochemicalmeasurementsshowedthattheactivationproperty,cyclingstabilityandself-dischargeofthealloyelectrodeswerealsoimprovedfortherapidsolidifiedalloys.TheHRDoftheas-castalloywasbetterthanthoseofalltherapidlysolidifiedalloys.Asthequenchingrateincreased,theHRDandexchangecurrentdensityfirstdecreasedandthenincreased.
简介:ApplicationoftheEu3+IonforSiteSymmetryDeterminationBinnemansK,Gorller-WalrandC(UniversityofLeuven,DepartmentofChemistry,Co?..
简介:TheLa3+-loadedadsorbentwaspreparedbythereactionbetweenLa3+andethanolamine-modifiedvegetabletannicextract,totreatF--containingwastewater.TheproblemsofheavycolorcausedbyvegetabletannicextractandofturbiditycausedbyreactionbetweenLa3+andF-weresolved.Whenotherconditionswerenotchanged,pH,temperature,stirringtime,anddosewerechangedrespectivelyandtheadsorbancewastestedrespectively.Theresultsshowthatthisadsorbentpossesseshighsaturatedadsorptivecapacity(18.86mg·g-1)whenpHis5~6,T≤80℃,0.2gdosage,and180minagitatingtime,andtheadsorbancereachesthehighest(98.5%).Theadsorbentcanbeeasilyregeneratedwith0.5mol·L-1NaOHatpH12.
简介:Praseodymium(Pr)wasimpregnatedtoCeO2-ZrO2solidsolutionbyanimpregnationmethod.Theas-obtainedPrmodifiedCeO2-ZrO2wasimpregnatedwith1wt.%Pdtopreparethecatalysts.ThestructureandreducibilityofthefreshandhydrothermallyagedcatalystswerecharacterizedbyX-raydiffraction(XRD),Raman,X-rayphotoelectronspectroscopy(XPS),COchemisorptionandH2temperature-programmedreduction(H2-TPR).Theoxygenstoragecapacity(OSC)wasevaluatedwithCOservingasprobegas.EffectsofimpregnatedPronthestructureandoxygenstoragecapacityofcatalystswereinvestigated.TheresultsshowedthattheagedPr-impregnatedsampleshadmuchhigherOSCandbetterreducibilitythantheunmodifiedones.TheschemeofstructuralevolutionsofthecatalystswithandwithoutPrwasalsoestablished.PartialoftheimpregnatedPrdiffusedintothebulkofCeO2-ZrO2duringageing,whichinhibitedthesintering,andincreasedtheamountofoxygenvacanciesinCeO2-ZrO2support.Furthermore,thoseimpregnatedPrspecieswhichcoveredonthesurfaceofthesupportobstructedthestrongmetal-supportinteractionbetweenPdandCesoastoreducetheencapsulationofPdaswellasthebackspill-overoftheoxygenduringthecatalyticprocess.
简介:采用浓HNO3/浓H2SO4混合酸在60℃超声环境下对T300碳纤维进行表面氧化处理,并以其为增强体制备碳纤维/环氧树脂复合材料。利用X射线光电子能谱仪、拉曼光谱仪、扫描电镜、原子力显微镜对表面氧化前后的碳纤维形态与表面化学性质进行表征,研究氧化时间对纤维的表面形貌与表面性质以及碳纤维/环氧树脂基复合材料力学性能的影响。结果表明,氧化初期,碳纤维表面生成S—、N—含氧基团,以及—OH和—C=O;后期形成—COOH,氧化时间为15min时,—COOH的浓度达到最大值。碳纤维/环氧树脂复合材料的强度随混合酸氧化时间延长而不断增强,氧化15min时强度达到峰值,相比于未氧化处理的样品,复合材料层剪切强度从16.3MPa提高到38.8MPa,抗弯强度从148.3MPa提高到379.7MPa。
简介:Theslidinggateusedtostopslagduringconvertertappingissimilartothecontrolofslidegateinladle,withtheslidinggatedeviceinstalledoutsidetheBOFtappingholetip.Owingtothequickopeningandclosing(in0.5s)oftheslidinggate,itcannotonlyeffectivelystopthepre-slagandpost-slagduringconvertertappingbutalsoautomaticallyjudgeandstopslagwiththehelpofAMEPAslagdetectingandPLCcontroltechnology.Currentlyitisregardedasthebestprocesstostopslagduringconvertertapping.