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:ThermodynamicmodelsofcalculatingmassactionconcentrationsforstructuralunitsorioncouplesinRbCl-H2ObinaryandRbCl-RbNO3-H2Oternarystrongelectrolyteaqueoussolutionsweredevelopedbasedontheionandmoleculecoexistencetheoryat298.15K.Atransformationcoefficientisneededtocomparethecalculatedmassactionconcentrationandthereportedactivitybecausetheyareobtainedatdifferentstandardstatesandconcentrationunits.TheresultsshowthatthetransformationcoefficientsbetweenthecalculatedmassactionconcentrationsandthereportedactivitiesofthesamestructuralunitsorioncouplesinRbCl-H2ObinaryandRbCl-RbNO3-H2Oternarystrongelectrolyteaqueoussolutionschangeinaverynarrowrange.ThetransformedmassactionconcentrationsofstructuralunitsorioncouplesinRbCl-H2Obinarysystemareingoodagreementwiththereportedactivities.ThetransformedmassactionconcentrationsofRbClandRbNO3inRbCl-RbNO3-H2Oternarysolutionarealsoingoodagreementwiththereportedactivities,aRbCland3RbNOa,withdifferenttotalionicstrengthsas0.01,0.05,0.1,0.5,1.0,1.5,2.0,3.0and3.5mol/kg,respectively.AllthoseresultsmeanthedevelopedthermodynamicmodelofstrongelectrolyteaqueoussolutionscanreflectstructuralcharacteristicsofRbCl-H2ObinaryandRbCl-RbNO3-H2Oternarystrongelectrolyteaqueoussolutionsandthemassactionconcentrationalsostrictlyfollowsthemassactionlaw.
简介:采用化学平衡模拟软件GEMS预测了锌湿法冶金过程中涉及的锌在Zn(Ⅱ)-NH3-H2O和Zn(Ⅱ)-NH3-Cl--H2O体系中的溶解度,并构建了其含锌物种分布图和优势区图。采用平衡实验方法测定了相同条件下锌的溶解度,其结果与预测结果相吻合。含锌物种的分布图和优势区图表明,在弱碱性条件下,2个体系均为以锌氨和羟基锌氨配合物为溶液的主要物种,其中Zn(NH3)24-为主要优势物种;在Zn(Ⅱ)-NH3-Cl--H2O体系中,锌氨氯三元配合物的形成能有效增大锌在中性条件下的溶解度,在该体系中存在Zn(OH)2、Zn(OH)1.6Cl0.4和Zn(NH3)2Cl23种固相,固相产物的形成取决于体系中总锌、总氨和总氯浓度。这些热力学平衡图表明了体系中各种物种之间的相互影响作用,并预测了总氨和总氯浓度的变化对锌溶解度的影响,为锌湿法冶金提供了热力学数据。
简介:Anewenvironmentalfriendlycatalyst,H4SiW12O40/PAnwaspreparedandidentifiedbymeansofFT-IR,XRDandTG/DTA.Cyclohexanone1,2-propanediolketalwassynthesizedfromcyclohexanoneand1,2-propanediolinthepresenceofH4SiW12O40/PAn.Thefactorsinfluencingthesynthesiswerediscussedandthebestconditionswerefoundout.Theoptimumconditionsare:molarratioofcyclohexanoneto1,2-propanediolis1:1.4,thequantityofcatalystisequalto1.0%offeedstocks,andthereactiontimeis40min.H4SiW12O40/PAnisanexcellentcatalystforsynthesizingcyclohexanone1,2-propanediolketalanditsyieldcanreachover96.5%.
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:1IntroductionTherareearthcobaltalloyshavethepotentialformakingthemagneticandmagnetoopticalmaterials.Sofar,therareearthcobaltalloyfilmsaresubstantiallyproducedbysputteringorvacuumplating.Ifsuchfilmsarepreparedbyelectrodepositioninstead,productionefficiencywouldbeimprovedandthecompositionofthealloycouldbecontrolled.Becausetheoxidationreductionpotentialsofrareearthelementsareverynegative,organicsolventsmaybeusedaselectrolyticmedia.ElectrodepositionofGdCoandSmCoinorganicsolutionshasbeenreporte...
简介:TiO2nanoparticleswithdifferentphasesarepreparedbyhydrolysisoftitaniumtetrabutoxideinthepresenceofHCl.ThecompositionandmicrostructureoftheresultingsamplesarestudiedbyXRDandTEM.TheseresultsshowthattherangeofparticlesizeofTiO2isfrom20to30nm.ThemechanismofTiO2photocatalysisreactionhasbeendiscussedextensively.PhotocatalyticactivitiesofnanometerTiO2arealsoevaluatedbydegradationofthecrystalvioletsolution.ExperimentalresultsindicatethatthesynergisticactionofH2O2andultrasonicwavegreatlyenhancesphoto-catalyticreactionofTiO2.
简介:有5-8nm的尺寸的做Eu的GaOOHnanoparticles被热水的方法作为表面活化剂用钠dodecylbenzenesulfonate(SDBS)准备。做Eu的-Ga2O3和-Ga2O3被退火进一步制作GaOOH:Eu然后由X光检查衍射(XRD)描绘了,传播电子显微镜学(TEM)和光致发光(PL)。TEM结果显示出那monodisperse做Eu3+的GaOOHnanoparticles形式然后变换进通过退火的做Eu3+的-Ga2O3和-Ga2O3GaOOH:在600和900点的Eunanoparticles?????????????????@
简介:为了分析含钒钛转炉渣氧压酸浸过程的热力学特点,根据高温水溶液中计算标准摩尔吉布斯自由能和活度系数的经验公式,通过计算得到了氧分压0.5MPa、对应离子的质量浓度0.1mol/kg、温度60~200℃条件下V-Ti-H2O系的电位-pH图。在pH〈2的酸性条件下,可溶性V3+,VO2+,VO2+的稳定区几乎全部包含在TiO2的稳定区范围内,随着温度由60℃升高到200℃,钒、钛稳定共存区对应的氧化还原电位逐渐增大,pH逐渐降低。钒、钛稳定区的共存特点从热力学角度为转炉渣采用氧压酸浸工艺通过一步酸浸将钒浸出的同时使钛富集在渣中提供了理论依据。含钒钛转炉渣的氧压酸浸实验结果表明,在浸出温度140℃、氧分压0.5MPa、粒度0.055~0.075mm、液固比15:1、浸出时间120min、搅拌速度500r/min、初酸浓度200g/L的条件下,钒的浸出率为96.87%,钛的浸出率为8.76%。钒与钛通过氧压酸浸工艺能够得到有效分离,实验结果与热力学计算结果一致。
简介:Themicrostructuresofas-castandas-solutionMg–12Gd–2Er–1Zn–0.6Zralloyswereinvestigatedbyopticalmicroscopy(OM),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),highresolutiontransmissionelectronmicroscopy(HRTEM)X-raydiffraction(XRD)andselected-areaelectrondiffraction(SAED)inthepresentinvestigation.TheresultsshowthattheprimaryeutecticphaseMg5(Gd,Er,Zn)andsomeflocculentfeaturesarefoundintheas-castalloy;theSAEDpatternindicatesthattheseflocculentfeaturesarethedenseareasofstackingfaults.The14H-LPSOstructureprecipitatesinthetemperaturerangeof673–793K,andthevolumefractionof14H-LPSOstructureincreaseswiththeextensionofheatingtime;however,thereisnoprecipitationof14H-LPSOstructurewhenthetemperaturereachesupto803K.Inaddition,theMg5(Gd,Er,Zn)phasedissolvesgraduallyalongwiththeprecipitationof14H-LPSOstructure.
简介:在H2SO4-Fe2(SO4)3体系中研究载金黄铁矿的浸出动力学,探讨反应温度、Fe3+浓度、硫酸浓度、搅拌速度等对黄铁矿浸出的影响规律。结果表明:在H2SO4-Fe2(SO4)3体系中,在30~75°C下黄铁矿浸出过程主要受化学反应控制Fe3+浓度与黄铁矿的浸出呈正相关,通过Arrhenius经验公式求得浸出表观活化能为51.39kJ/mol。EDS与XPS分析结果表明:黄铁矿氧化过程中硫的氧化经一系列中间形态,最终被氧化成硫酸根,并伴有部分元素硫生成,符合硫代硫酸根氧化路径机理。
简介:提出一种从黑泥中回收利用钛的新工艺,该工艺包括NaOH水热转化、水洗和H2SO4浸出制备TiO2。在优化的反应条件下,即NaOH溶液浓度为50%(质量分数)、NaOH/黑泥质量比为4:1、反应温度为240°C、反应时间为1h和氧气分压为0.25MPa,钛转化率可达97.2%,主要含钛产物是Na2TiO3。非目标产物Na2TiSiO5在水洗中保持稳定,在水热反应中提高NaOH浓度可以抑制Na2TiSiO5的生成。水热产物经过水洗后,97.6%的Na^+可以回收。含有NaOH的溶液经过浓缩之后可以回用。在较低温度下,水洗物料中96.7%的钛能被较低浓度的硫酸浸出得到钛液。利用所得钛液进一步制备合格TiO2产品。