简介:TiO2nanoparticleswithdifferentphasesarepreparedbyhydrolysisoftitaniumtetrabutoxideinthepresenceofHCl.ThecompositionandmicrostructureoftheresultingsamplesarestudiedbyXRDandTEM.TheseresultsshowthattherangeofparticlesizeofTiO2isfrom20to30nm.ThemechanismofTiO2photocatalysisreactionhasbeendiscussedextensively.PhotocatalyticactivitiesofnanometerTiO2arealsoevaluatedbydegradationofthecrystalvioletsolution.ExperimentalresultsindicatethatthesynergisticactionofH2O2andultrasonicwavegreatlyenhancesphoto-catalyticreactionofTiO2.
简介:Iron(Ⅲ)-dopednanostructureTiO2-coatedSiO2(TiO2/SiO2)particleswerepreparedusingthelayer-by-layeras-semblytechniqueandtheirphotocatalyticpropertywasstudied.TiO2colloidsweresynthesizedemployingthesol-gelmethodwithTiCl4asaprecursor.ThesampleswerecharacterizedbyFouriertransforminfraredspectroscopy(FTIR),SEM,EDS,XPS,andXRD.TheexperimentalresultsshowthatTiO2nanopowdersonthesurfaceofSiO2particlesarewelldistributed,theamountofTiO2isincreasedwiththeaddingofcoatinglayers,thepureanatase-TiO2coatinglayersaresynthesizedat500°C,andthephotocatalyticactivityofFe3+-dopedTiO2/SiO2ishigherthanthatofundopedTiO2/SiO2.
简介:Nb-24Ti-18Si-2Al-2Hf-4CrandNb-24Ti-18Si-2Al-2Hf-8Cralloyswerepreparedbyarcmeltinginawater-cooledcrucibleunderargonatmosphere.Microstructuralcharacteristicsandoxidationresistanceofthealloysat1250℃wereinvestigated.Theresultsshowthat,whentheCrcontentis4at%,themicrostructuresconsistof(Nb,Ti)_(ss)andNb_5Si_3;asCrcontentincreasesto8at%,C14LavesphaseCr_2Nbisformed.Theisothermaloxidationtestsshowthattheoxidationkineticsofthetwoalloysfollowsimilarfeatures.Theweightgainsofthetwoalloysafteroxidationat1250℃for100hare235.61and198.50mg·cm~(-2),respectively.Duringoxidation,SiO_2,TiO_2,Nb_2O_5andCrNbO_4areformedatfirst.Then,Ti_2Nb_(10)O_(29)isformedafteroxidationfor20minandbeginstochangeintoTiNb_2O_7astheoxidationproceeds.SiO_2isformedassolidstateatfirstbutlaterevolvesintoglassystatetoimprovethecohesionofthescale.Afteroxidationfor100h,oxidationproductsconsistofSiO_2,TiNb_2O_7,Nb_2O_5andCrNbO_4.
简介:ElectrocrystallizationMechanismofTungsteninMoltenKF-B_2O_3-K_2WO_4WenZhenhuanandLiGuoxun文振环,李国勋(GeneralResearchInstiiuteforNo...
简介:介绍一种金属/合金的生产方法,用于恒电流和恒电位条件下由混合硫化物(Cu2S,NiS)生产Cu-Ni合金,称为直接电化学还原(DER)。研究槽电压和槽电流等工艺参数对还原得到的化合物组成的影响,以生产工业所需的CuNi10,CuNi20和CuNi30等合金。在1200°C下采用循环伏安法(CV)考察Cu2S和NiS在CaCl2熔体中的电化学行为。根据CV研究结果,Cu2S的阴极还原是一步完成的,即Cu2S?Cu;NiS的阴极还原则分两步进行,即NiS?Ni3S2?Ni。恒电流研究表明,在10A电流下电解15min,可制备出最高硫含量为320×10-6的高纯CuNi10合金。扫描电子显微镜以及能量色散X射线能谱和光学发射光谱(OES)测试结果表明,在2.5V电压下直接电化学还原15min,可制备出杂质含量低(即硫含量小于60×10-6)的所选成分的Cu-Ni合金。
简介:本文采用磁粉、X射线、CT和超声等无损检测和金相分析等方法对40CrNi2Si2,MoVA钢制零件的磁痕显示进行了系统分析。研究认为,40CrNi2Si2MoVA钢制零件的磁痕显示为显微成分沿变形方向偏析导致的马氏体转变点Ms差异所致。显微成分偏析是钢锭结晶过程中不可避免的,但可通过优化熔炼工艺参数降低显微偏析的程度。本文还分析了四种磁痕显示的类型及其判别方法。
简介:Themetal-organicchemicalvapordeposition(MOCVD)techniqueisapromisingprocessforhigh-temperaturesuperconductorYBa2Cu3O7-δ(YBCO)preparation.Inthistechnique,itisachallengetoobtainbariumprecursorswithhighvolatility.Inaddition,thepurity,evaporationcharacteristics,andthermostabilityofadoptedprecursorsinwholeprocesswilldecidethequalityandreproducibleresultsofYBCOfilm.Inthepresentreport,bis(2,2,6,6-tetramethyl-3,5-heptanedionato)barium(Ⅱ)(Ba(TMHD)2)wassynthesized,anditsstructurewasidentifiedbyFTIR,1HNMR,13CNMR,andESI-MSspectroscopy.Subsequently,thethermalpropertiesandthekineticsofdecompositionweresystematicallyinvestigatedbynonisothermalthermogravimetricanalysismethods.BasedontheaverageapparentactivationenergyevaluatedbytheOzawa,Kissinger,andFriedmanmethods,thevolatilizationprocesswasdiscussed,andallresultsshowthatBa(TMHD)2isunstableandhighlysensitivetothechangeoftemperatureduringthewholeevaporationprocess.Therefore,itisveryimportanttochoosesuitablevolatilizationtechnologyandconditionsforavoidingBa(TMHD)2break-down(orthermalaging)duringMOCVDprocess.Subsequently,thepossibleconversionfunctionisestimatedthroughtheCoats-Redfernmethodtocharacterizetheevaporationpatternsandfollowsaphaseboundaryreactionmechanismbythecontractingsurfaceequationwithaverageactivationenergyof118.7kJ.mol-1.
简介:起落架40CrNi2Si2MoVA钢螺桩在安装一段时间后发生了断裂。为确定螺桩断裂的原因,对断裂螺桩断口宏微观形貌、断裂螺桩及对比件的氢含量、材料的性能以及表面损伤等因素进行了检查,并对电镀工艺进行了评定。结果表明,裂纹主要起源于第一螺纹根部的机械损伤部位,源区以沿晶断裂特征为主,断裂件含氢量较高。综合分析认为。螺桩断裂性质为氢致延迟断裂,表面机械损伤对氢吸收和扩散的促进作用和40CrNi2Si2MoVA钢材料高强度所致的高氢脆敏感性是导致断裂的主要原因。
简介:通过基于密度泛函理论的第一性原理计算方法,对MgCu2,Mg2Ca和MgZn2的力学性能和电子结构进行计算,计算所得晶格参数与实验值和文献值相吻合。合金形成热和结合能的计算结果表明,MgCu2具有最强的合金形成能力和结构稳定性。计算了MgCu2,Mg2Ca和MgZn2的弹性常数,推导了体模量、剪切模量、弹性模量和泊松比。结果表明,MgCu2、Mg2Ca和MgZn2均为延性相,MgCu2的刚度最大,MgZn2的塑性最好。通过对结合能和弹性常数的计算,预测了MgCu2、Mg2Ca和MgZn2的熔点。通过对态密度(DOS)、Mulliken布居数、电子占据数和差分电荷密度的计算,分析了MgCu2、Mg2Ca和MgZn2的结构稳定性和力学性能机制。最后,计算和讨论了3种金属间化合物的Debye温度。
简介:ItiswellknownthatthephotocatalyticactivityofTiO2thinfilmsstronglydependsonthepreparingmethodsandpost-treatmentconditions,sincetheyhaveadecisiveinfluenceonthechemicalandphysicalpropertiesofTiO2thinfilms.Therefore,itisnecessarytoelucidatetheinfluenceofthepreparationprocessandpost-treatmentconditionsonthephotocatalyticactivityandsurfacemicrostructuresofthefilms.ThisreviewdealswiththepreparationofTiO2thinfilmphotocatalystsbywet-chemicalmethods(suchassol-gel,reversemicellarandliquidphasedeposition)andthecomparisonofvariouspreparationmethodsaswellastheiradvantageanddisadvantage.Furthermore,itisdiscussedthattheadvancementofphotocatalyticactivity,super-hydrophilicityandbactericidalactivityofTiO2thinfilmphotocatalystinrecentyears.
简介:Thesegregationanddiffusionofboronduringheattreatmentswerestudied.Theinfluenceofboroncontents,agingtimeandappliedstressonFeMo2B2formationwasalsostudied.Finally,theeffectsofboroncontentsandFeMo2B2formationonthehightemperaturestrengthwerestudied.Boronatomsweresegregatedtoprioraustenitegrainboundaryduringnormalizingtreatment.Andtheseboronatomswereslowlydiffusedintothegraininteriorduringtemperingandagingat700℃.TheFeMo2B2phasewasonlyformedafter1,000hagingat700℃inalloycontaining196ppmboron.TheformationofFeMo2B2phaseisacceleratedbytheappliedstress.ItwasexpectedthattheformationofFeMo2B2iscloselyrelatedtotheredistributionofboronatoms.Thetensilestrengthsat700℃areincreasedwiththeincreaseofboroncontents.However,theformationofFeMo2B2phaseresultsinlowertensilestrength.
简介:TheeffectofyttriaonthesolidreactionmechanismofaCaHPO4·2H2O+CaCO3systematdifferenttemperatureswasexperimentallystud-ied.Thesampleswithandwithoutyttriaweresubjectedtothermogravimetric/differentialscanningcalorimetrymeasurement.ThesampleswereheattreatedatthetemperaturescorrespondingtothepeaksontheDSCspectra,andtheresultedphasecompositionswereidentifiedbyX-raydiffraction.Thetransformationmechanismwasdeducedbycomparingthephasesobtainedatdifferenttemperatures.Theresultsshowthatthetransformationsatbelow1073Karenotaffectedbyyttria,butallthoseatabove1073Karecompletelyaltered.Theformationtem-peratureofhydroxyapatitedecreasesby134K,andthedecompositiontemperatureincreasesby38K.ThepolymorphoustransformationofCa3(PO4)2fromβphasetoαphaseincreasesby47K.Thethermodynamicpropertiesofthetransformationsatabove1073Karealsomodi-fiedbytheadditionofyttria;thatis,theendothermalpeaksaresubstitutedbyexothermalpeaks.
简介:TiO2/Au/TiO2多层的薄电影用dc(直接水流)在房间温度在聚合物底层被扔磁控管劈啪作响方法。由改变每层的厚度,TiO2/Au/TiO2多层的电影的光、电的性质能被定制适合不同应用。厚度和Au层的光性质和Au绝缘的接口的质量为Au绝缘的多层的薄电影的电、光的表演是批评的。在8nm的厚度,Au层形成有最低抵抗力和它的连续结构一定为高发射度薄。多层的栈能被优化有6的一个表电阻?在在在波长的680nm的超过80%的发射度的/sq.。当时,山峰发射度向长波长区域变二TiO2的厚度(上面、更低)层增加。当二部TiO2电影的电影厚度是45nm时,高发射度价值为全部可见轻波长区域被获得。
简介:利用高频辅助激光熔覆技术在镍基合金上制备Al2O3-13%TiO2(质量分数)陶瓷涂层。采用SEM、XRD和EDS等方法分析陶瓷涂层的微观结构和陶瓷层与粘结层之间的结合界面。结果表明:陶瓷层出现了完全熔化区和液相烧结区双层结构,其中,完全熔化区颗粒充分烧结长大,而液相烧结区则出现了三维网状结构,该三维网状结构由熔化的TiO2相包裹Al2O3颗粒形成。通过激光熔覆作用下的粉末熔化和扁平化行为解释双层结构形成机理。同时,在陶瓷层与粘结层的结合界面上发现具有尖晶石结构的NiAl2O4和针状结构的Cr2O3,证明在激光熔覆过程中发生的化学反应可以有效增加陶瓷层与粘结层的结合强度。
简介:为提高硼的去除率,研究了电磁感应精炼过程中硼杂质在CaO-SiO2-BaO-CaF2四元渣和熔硅之间的分配系数LB,讨论了四元渣系中CaO/SiO2质量比、BaO和CaF2含量、熔炼时间对LB的影响规律。结果表明:随着CaO.SiO2渣中BaO和CaF2含量的增大,LB值增大。当CaO/SiO2质量比为1.1:1、BaO和CaF2含量分别为15%和20%时,CaO.SiO2.BaO.CaF2四元渣去除熔硅中硼杂质效果最好,LB达到最大值6.94,并且LB随着熔炼时间的延长而增大。经过两次造渣后,熔硅中硼含量由3.5×10.5降到3.7×10.6,硼的去除率达到89.4%。
简介:Inviewoftheimportanceofsolventextractionofrareearthmetalswiththeacidicorganophosphorousreagent,thedevelopmentofachemicallybasedmodelapplicabletohighconcentrationisdesired.Inthepresentstudy,theequilibriumdistributionofdysprosium(Ⅲ)betweenanaqueousnitricacidsolutionand2-ethylhexylphosphonicacidmono-2-ethylhexylester(PC88A)wasmeasuredintherangeofaninitialaqueousdysprosium(Ⅲ)concentrationfrom1.0×10-3to1.0×10-1kmol/m3andPC88Aconcentrationfrom0.16to0.65kmol/m3inShellsolD70asthediluent.Theobtaineddatawereanalyzedusingthechemicallybasedmodelinordertocorrelatetheequilibriumdistributionratios.Inthismodel,dysprosium(Ⅲ)wasassumedtobeextractedwiththePC88Adimerasa1:3complex,theactivitieswereconsideredfortheaqueousspecies,andtheeffectiveconcentrationofthePC88AdimerwascalculatedusingAlstad'sempiricalequation.Asaresult,theapparentextractionequilibriumconstantwasdeterminedtobe253(kmol·m-3)-2withanexcellentcorrelationbetweentheexperimentandcalculationresultsinthewiderangeofthelogarithmofthedistributionratiofrom-2to3.5.Inconclusion,themethodologyinthismodelwouldbeeffectiveforquantitativedescriptionofsolventextractionbehaviorofgeneralrareearthelementsaswellasdysprosium.