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:BondingofAl2O3tocuisperformeddirectlyusingTifoilattemperatureof1273K.Themicrostructureofthejointinterfaceisinuestigatedthroughscanningelectronmicroscope(SEM),electron.probemicroanalysis(EPMA)andX-raydiffraction(XRD).theeffectoftheinitialtifoilthicknessonthereactionlayerthicknessandthejointStrengthareinvestigated.
简介:通过涂覆热分解法制备了Ti/RuO2-ZrO2-SnO2、Ti/RuO2电极材料,采用X射线衍射(XRD)、扫描电镜(SEM)和循环伏安(CV)对电极材料进行表征,考察了电流密度、NaCl质量浓度、pH值及电极间距对废水COD降解率的影响。结果表明,Ti/RuO2-ZrO2-SnO2电极对COD具有更高的降解率,对其进行工艺优化。电极材料对废水降解的最佳工艺条件为电流密度40mA/cm^2,NaCl质量浓度4g/L,pH=5.0,电极间距10mm,COD的降解率达到90.5%。Ti/RuO2-ZrO2-SnO2电极中SnO2与RuO2生成固溶体,有利于增强涂层与基体之间的结合力,提高电极的稳定性;ZrO2起到细化晶粒的作用,致使电极表面粗糙度增加,增强了电极的电催化性能,且降解过程符合一级动力学模型。
简介:Anovelhighgravitymulti-concentriccylinderelectrodes-rotatingbed(MCCE-RB)wasdevelopedfortheelectrocatalyticdegradationofphenolwastewaterinordertoenhancethemasstransferwiththeself-madeRuO2-IrO2-SnO2/Tianodes.Theinfluencesofelectriccurrentdensity,inletliquidcirculationflowrate,highgravityfactor,sodiumchlorideconcentration,andinitialpHvalueonphenoldegradationefficiencywereinvestigated,withtheoptimaloperatingconditionsdetermined.Theresultsshowedthatundertheoptimaloperatingconditionscoveringacurrentdensityof35mA/cm^2,aninletliquidcirculationflowrateof48L/h,ahighgravityfactorof20,asodiumchlorideconcentrationof8.5g/L,aninitialpHvalueof6.5,areactiontimeof100min,andaninitialphenolconcentrationof500mg/L,theefficiencyforremovalofphenolreached99.7%,whichwasimprovedby10.4%ascomparedtothatachievedinthenormalgravityfield.Thetendencyregardingthechangeinefficiencyforremovalofphenol,totalorganiccarbon(TOC),andchemicaloxygendemand(COD)overtimewasstudied.Theintermediatesanddegradationpathwayofphenolwerededucedbyhighperformanceliquidchromatography(HPLC).
简介:目的新型表面改性技术和改性材料的开发是当今生物医学材料研究的主要方向,羟基磷灰石(HA)是一种最重要的表面改性材料,但较高的脆性和较低的结合强度严重制约了它在临床中的应用.方法本研究首次选用K2Ti6O13作为生物医用Ti合金的表面改性材料,利用KDC法尝试制备了K2Ti6O13涂层,并对涂层的微结构、结合强度和生物活性进行了观察分析与评估.结果利用KDC方法可以成功地原位合成K2Ti6O13涂层,涂层与钛合金基体间结合牢固,结合强度可达24MPa,热膨胀系数的良好匹配是结合强度提高的主要原因.结论涂层粗糙的表面和气孔可为骨的向内生长提供有利位置.经模拟体液浸泡,涂层表面形成了钙磷比接近人体骨骼的钙磷层,表明涂层具有良好的生物活性.
简介:TheepoxidationofallylchloridewithH2O2onTi-ZSM-5preparedbyisomorphoussubstitutionofHZSM-5withTiCl4gaswasstudied.TheresultsshowthatTi-ZSM-5hasahighcatalyticefficiencyfortheepoxidationofallylchloride.TheH2O2utilizationreaches99.50%whentheallylchloride/H2O2molarratiois>1.Theeffectofsolventspecies,catalystconcentration,H2O2andallylchlorideconcentrationandreactiontemperatureontheepoxidationwasinvestigatedsimultaneously.Itisfoundthatmethanolisthebestsolventforthereaction.Thereactionrateequationwithv=k[Cat.][H2O2]1/2-[C3H5Cl]andtheapparentactivationenergywithEa=63.462kJ/molareobtainedaccordingtothekineticsstudy.
简介:利用线性伏安法和恒电流电解法研究了苯酚在Ti/PbO2电极上的电催化氧化反应,通过电氧化过程中反应物和中间物的高效液相色谱测定,研究了苯酚在Ti/PbO2电极上电催化氧化的反应机理.实验发现,Ti/PbO2电极对水溶液中苯酚的电氧化具有显著的催化作用,25℃时,对初始浓度为2mmol/L的苯酚水溶液,恒定电流密度为50mA/cm2,电解3h,苯酚转化率为98.02%,有机碳去除率为54.36%.苯酚在Ti/PbO2电极上电催化氧化要经过对苯二酚或邻苯二酚、对苯醌、反丁烯二酸和草酸,最终变成二氧化碳和水的历程.第一步反应苯酚转化的主产物是对苯二酚.对苯二酚转化为苯醌和苯醌转化为反丁烯二酸的反应为慢反应,反丁烯二酸转化为草酸的反应为快反应.
简介:PhotocatalyticH2productionhasemergedasoneofthemostcleanandpromisingrenewableenergysources.InspiteoftheeffortstoobtainefficientphotocatalystsabletoproduceH2fromSunlightandwater,thereisstilltheneedtopreparecheaperandenvironmentalfriendlierphotocatalysts.Phosphatebasedmaterialscouldbegoodcandidatestofulfilltheserequirements.InthismanuscriptwehavepreparedasetofmixedTi3+/Ti4+valence,open-frameworktitaniumphosphates(of-TiPO4)andmixedtitaniumoxide/phosphatederivatives(cr-TiP),correlatingtheirstructureandcompositionwiththephotocatalyticactivityforH2production.Wedeterminedthatmixedtitaniumoxide/phosphatecrystallinephasesproducedenhancedH2evolutionunderSunsimulatedlightirradiationthanmixedTi3+/Ti4+valence,open-frameworktitaniumphosphatesandtitaniumoxidephases.
简介:采用反应合成方法制备孔隙度为54.3%的高纯Ti3SiC2多孔材料,并研究其在400~1000°C下空气中的氧化行为。采用热重-差热分析法、扫描电镜、X射线衍射技术、能谱仪、拉曼光谱、BET比表面分析法和孔结构测试等研究Ti3SiC2多孔材料在氧化前后的氧化动力学、物相组成、微观形貌以及孔结构参数演变。结果表明:形成不同晶型TiO2氧化产物是影响Ti3SiC2多孔材料抗氧化性及孔结构稳定性的主要因素。由于氧化产物体积应力以及热应力的存在,因此,在400~1000°C试验过程中试样表面均出现开裂现象。其中,在400~600°C下形成的锐钛矿型TiO2会导致Ti3SiC2晶粒出现严重开裂,并引发快速氧化以及孔径和透气度的异常减小。600°C以上在氧化过程中主要形成金红石型TiO2,开裂现象得以缓解,但是氧化膜的外延生长大幅降低了Ti3SiC2多孔材料孔隙的连通性。
简介:TiO2nanoparticlesweresynthesizedbyahomogeneouscontrolledprecipitationmethodusingindustrialtitaniumsulfate(Ti(SO4)2).TheobtainedpowderswerecharacterizedbyX-raydiffraction(XRD),transmissionelectronmicroscope(TEM),Fouriertransforminfraredspectroscopy(FTIR)andICPplasmaspectrometer.EDTAwasusedascomplexingagenttoimprovethepurityandtheformationofTiO2nanoparticles.Experimentalresultsindicatedthatthehigh-purityTiO2nanoparticleswere20nminmeansizeandnearlymonodispersed.