简介:Solventextractionofpalladium(Ⅱ)fromhydrochloricacidsolutionwith2-n-octyl-4-isothiazolin-3-one(OIT)/cyclohexanewasstudied.Effectsofdifferentparametersonextractionefficiencywereevaluated.99.96%and98.26%palladium(Ⅱ)couldbeeffectivelyextractedwith0.018mol·L-1OIT/cyclohexaneof0.1and4.0mol·L-1HClmedium,respectively.Nonpolarsolventandlowaciditycouldimprovetheextractingefficiency,andsuccessfullystrippalladium(Ⅱ)fromtheloadedorganicphasewasachievedwith0.5mol·L-1(NH2)2CSsolution.ItwasproposedthattheextractionofPdcomplexesfromHClmediumproceededthroughtheionassociationmechanismbyslopemethod,NMRandFT-IRspectra.
简介:AnewtypeofcomplexsolidsuperacidcatalystWO3-ZrO2-SO42-withanacidstrengthH0≤-16.04waspreparedbykneadingZr(OH)4oramorphousZrO2withtungsticacid(H2WO4)(W/Zr=0.15),followedbyexposingthiscomplexhydroxidesto0.5tool/LH2SO4,calcininginairat700~800℃for3h.ThiscatalystpossessesbothstrongBronstedacidityandstrongLewisacidityexperimentallyshowedbyIRobservationofpyridineabsorbedonit.XPSandAEStechniqueswereemployedtoexaminethevalencestatesoftungsten,zirconium,sulfurandtheirinteractions.Thestructureofsulfurspecieswasstudiedbyinfraredspectroscopyandastructuremodelofactivesitewasproposedupontheseresults.
简介:TheHAZmicrostructureandperformanceofQuenchingandTemperingmodetemperbeadweldingandgeneralweldedjointswhichweremadeonSA508-3steelof60mmthicknesswerecomparedinthisarticle.Theresultshowsthattemperingsorbitewhichhasexcellentoverallperformancewasobtainedinbothmodes.ThemicrostructureofQuenchingandTemperingmodeweldedjointsgotmorefinegrain.Eventhoughthehardnessoftemperingbeadweldedjointsishigherthanthegeneralone,itstillmeetsthestandardswhichislowerthan350HV.TheimpactabsorbingenergyofeachdistrictoftemperingbeadweldedjointsHAZreached170J,whichisequaltogeneralone.
简介:Fe(OH)3precursorsolwaspreparedbyasol-gelmethod.Theprecursorsolwasdippedontotheabsorbentcotton,andgelwasformedontheabsorbentcottontemplateafterthevolatilizationofmoisture.Fe2O3microtubulesweresynthesizedaftertheprocessofself-propagationorcalcination.Thephase,morphology,andparticlediameterofthesampleswereexaminedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM),andthemagneticpropertiesofthesamplesweremeasuredusingavibratingsamplemagnetometer(VSM).TheexternaldiametersofFe2O3microtubulesrangedbetween8and13μm,andthewallthicknessesrangedbetween0.5and2μm.ThetypeofthecalcinationmethodplaysasignificantroleindevelopingtheFe2O3phaseandthevariationinthemagneticpropertiesinthesol-geltemplatecomplexingmethod.γ-Fe2O3wassynthesizedbyaself-propagationmethod.However,α-Fe2O3wassynthesizedaftercalcinationat400°Cfor2h.Thecoercivityofthesamplessynthesizedbycalcinationat400°Cfor2hafterself-propagationwasfoundtoincreasesignificantly,therebypresentinghardmagneticproperties.
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:Pt(Ⅱ)andPd(Ⅱ)complexeswith2',3',4',5,7-pentahydroxy-flavoneweresynthesizedandcharacterizedbyelementalanalysis,molarconductance,IR,1HNMR,TG-DTA,UV-Visspectroscopictechniques,andfluorescenceanalysis.Thescavengingeffectonthesuperoxideradical(O-2)andtheinhibitoryeffectonlipidperoxideswerealsoinvestigated.Boththeligandandthecomplexesexhibitscavengingeffectonsuperoxideradicals,andtheeffectofthecomplexesisgreaterthanthatoftheligand.ThePt(Ⅱ)complexexhibitsthestrongestscavengingefficiency.BothPt(Ⅱ)andPd(Ⅱ)complexeshavetheinhibitoryeffectonlipidperoxides,andtheeffectofthecomplexesisgreaterthanthatoftheligand,butthePt(Ⅱ)complexhasahigheffectofpromotinglipidperoxides.
简介:Fe3AlandCr18-Ni8steelwerebondedinvacuumandaninterfacewasformedbetweenFe3AlandCr18-Ni8steel.Stressdistributionatthediffusion-bondedinterfacewasresearchedbynumericalsimulationandfiniteelementmethod(FEM).TheresultsindicatedthatthepeakstressappearedattheinterfacenearCr18-Ni8steelside.Thisisthekeyfactortoinducecrackatthisposition.Withtheenhancementofheatingtemperature,thepeakstressatthebondedinterfaceincreases.Whenthetemperatureis1100℃,thepeakstressisupto65.9MPa,whichisbiggerthanthatat1000℃by9.4%.Inaddition,thepeakstressbecomesbiggerwiththeincreaseofthethicknessofbasemetalfrom1mmto8mm.Whilethethicknessismorethan8mm,thepeakstressvariesslightlywiththechangeofthethickness.