简介:Aseriesofthecoconutactivatedcarbons(CAC)basedabsorbentsmodifiedwithCuandCe(Cu/CAC,Cu/Ce/CAC)werepreparedbyimpregnationtechnologyforcarbondioxidecapture.TheadsocrptionequilibriumsofCO2onCu/CACandCu/Ce/CACweremeasured.TheresultsshowedthattheadsorptioncapacityofCO2ontotheactivatedcarbonmodifiedwithCu/Ceincreasedwiththedecreasingtemperatureinthesamepressure.TheadsorptioncapacityofCO2onCu/CACwashigherthanthatoftheblankCAC,andcomparedwiththeCu/CAC,theadsorptioncapacityofCO2ofCu/Ce/CACwiththemassratioofCu/Ce=30wasimprovedat298and303K.Inaddition,theadsorptionequilibriumdataforCO2atvarioustemperatureswasfittedtoLangmuir,FreundlichandD-Risothermmodels.ItwasfoundthattheD-RequationwasthebestmodelforfittingtheadsorptiondataonCu/Ce/CACatdifferenttemperatures.
简介:VariousopticalluminescencespectroscopictechniqueswereusedtocharacterizethehighTcsuperconductorYBa2Cu3Ox.TheemissionbandsrevealthatCu3+coexistwithCu2+andCu+inthismaterial.
简介:Fe/Cu/Cemodifiedcoal-basedactivatedcarbon(AC)waspreparedbythesol-gelmethod,andtheeffectofFe/Cu/CeoncatalyticpropertiesofFe/AC,Fe-Cu/ACandFe-Cu-Ce/ACwasinvestigatedinthehydrolysisofcarbonylsulfide(COS)at50°C.Theirsurfacepropertieswereevaluatedbymeansofnitrogenadsorptionandwerecharacterizedbyusingscanningelectronmicroscopy(SEM),X-raydiffracto-metry(XRD)andX-rayphotoelectronspectroscopy(XPS).ThecatalyticactivitiesresultsshowedthatadditionofCuandCe...
简介:Aseriesofcoal-basedactivecarbon(AC)catalystsloadedbyFe-Cu,Fe-Cu-CeandFe-Cu-Lawerepreparedbythesol-gelmethodforcarbondisulfide(CS2)hydrolysisandtheirperformancesforCS2hydrolysisinafixed-bedreactorwereinvestigatedinthiswork.TheresultsshowedthatthekindofrareearthoxideanditscontenthadobviouseffectonhydrolysisremovalofCS2.Theeffectsoftemperature,spacevelocity,CS2concentrationandO2concentrationwerealsodiscussedrespectively.Furthermore,thesuitableoperatingconditionswereobtained.Itwasfoundthatthepoisoningofhydrolysisactivesitescouldresultintheformationofsulfuricacidonthecatalystsurface.
简介:Theaimofthisresearchistopulseco-depositnano-CeO2particlesintoNi-W-Balloycoatingsinordertoimprovethesurfaceproperties.Theinfluenceofpulsefrequencyanddutycircleondepositionrate,microhardnessandmicrostructures,andtheinfluenceofheattreatmenttemperatureonphasestructures,microhardnessandabrasivityofNi-W-B-CeO2compositecoatingswereinvestigated.Theresultsindicatedthatthepulseco-depositionofnickel,tungsten,boronandnano-CeO2particlefromthebathwhichnano-CeO2particlewassuspendedbyhighspeedmechanicalstirringledtotheNi-W-B-CeO2compositecoatings,possessingbettermicrohardnessandabrasionresistancewhenheat-treatedat400℃for1h.Themicrohardnessas-depositedwith636Hzandthedepositionratewith0.0281mm·h-1wasthehighestatpulsefrequencywith1000Hzandpulsedutycirclewith10%.Microstructuresanalysisdisplaysthatdecreasingpulsedutycycleleadstorefinementingrainstructuresandtheimprovementofmicrostructures.X-raydiffractionshowsthatthecompositecoatingas-depositedwasmainlyintheamorphousstateandpartiallycrystallized,butwhenheattreatedat400℃,thecrystallizationtrendwasstrengthenedfurther.
简介:试图为高温度的熔融的盐反应堆的安装和电极的建设开发材料,在750和950湩爠晥湩浥湥?瑳敲杮桴湥湩?猠汯摩猠汯瑵潩?瑳敲杮桴湥湩?眠牯?慨摲湥湩?愠摮瀠敲楣楰慴楴湯猠牴湥瑧敨楮杮的Ni-11Fe-10Cu的高温度的氧化行为上的艾尔和Y的效果
简介:Phosphine(PH3)isahighlytoxicairpollutant,commonlyproducedinphosphorouschemicalindustry.Butithasreceivedlessresearchattentionduetoitshandlingdifficultly.COisthemaincontentofthephosphorouschemicalindustrytailgas,theconcentrationofwhichisalwaysmorethan80vol.%,anditcanbethefeedgastoproducevariousvaluableproductssuchasformate,oxalate,andmethanolandsoon.But,PH3isoneoftheimportantbarriers,whichisharmfultothefollowingchemicalprocess.Inordertomakeuseofthetailgas,PH3shouldberemovedfirstly,andCOshouldbecoveredinthewholepurifiedprocedureatthesametime.Inthiswork,themodifiedactivatedcarbon(MAC)wasusedastheadsorbenttoseparatePH3fromthemixturetailgas.SeriesofMACadsorbentswerepreparedfortheadsorptionofPH3,whichloadedCu-FeandCe(La),orseparately.ThePH3adsorptioncapacities,chemicalandphysicalpropertiesofMACwereallinvestigated.Theresultsshowedthatover99%PH3adsorptionefficiencywasachievedwhenusedMACadsorbents.TheremovalefficiencyandPH3adsorptioncapacityoftheCu-Fe-Ce/AC(20:1:0.4)werebothmuchhigherthanthosemodifiedactivatedcarbons.ThemaximumPH3adsorptioncapacitywas71mgofPH3/gofMAContheCu-Fe-Ce/AC,whichweremuchhigherthanliteraturedatausingCuOonlyforadsorbinghydridegases.
简介:采用化学共沉淀法来制备ITO纳米粉末,探讨了反应终点pH值(分别为7,8及9)和煅烧温度(分别为350℃,650℃,750cc及850℃)对ITO粉体性能的影响,借助TG—DSC、XRD、SEM、HRTEM、FT-IR等分析手段对粉体进行了表征。得到如下结论:在液相中加入硅酸钠,反应温度为60℃,反应终点pH值为8,老化制度为60min,煅烧制度为750℃/2h的工艺条件下,所制得的ITO纳米粉不含SnO2相,呈显著的单相结构,是一种立方结构的In2O3固溶体;粉体粒径在30—60nm之间,比表面积为34.26m^3/g,形貌为近球形,颗粒均匀,且分散性能良好,在波数840—3164cm。范围内对红外光的反射率高达66%~94%。
简介:Ni-W-P-CeO2-SiO2nano-compositecoatingswerepreparedonthecarbonsteelsurfacebypulseco-depositionofnickel,tungsten,phosphorus,nano-CeO2andnano-SiO2particles.Theinfluenceofnano-SiO2particlesconcentrationsinelectrolyteonmicrostructuresandpropertiesofthenano-compositecoatingswereresearched,andthecharacteristicswereassessedbychemicalcompositions,elementdistribution,depositionrate,microhardnessandmicrostructures.Theresultsindicatethatwhennano-SiO2particlesconcentrationsinelectrolytearecontrolledat20g·L-1,thedepositionratewith27.07μm·h-1andthemicrohardnesswith666Hvofthenano-compositecoatingsarehighest,elementlinescanningandareascanninganalysesshowthattheaveragecontentsofelementsW,P,SiandCeinthenano-compositecoatingsareclose,displayingthatthedistributionofeveryelementwithinthenano-compositecoatingsiseven.Anincreaseinnano-SiO2particlesconcentrationsinelectrolyte(whenlowerthan20g·L-1)leadstorefinementingrainstructureofnano-compositecoatings,butwhenitimprovedto30g·L-1,thecrystallitesizesincreaseagainandinthemeantimetherearealotofsmallbosswithnodulationshapeappearingonthesurfaceofnano-compositecoatings.
简介:(Cu60Zr30Ti10)98Y2bulkmetallicglass(Φ4mm×70mm)wasobtainedsuccessfullybycoppermouldcoolingandspraying-casting,andsomesampleswereisothermallyannealedattemperaturesof473and623K,whichwaslowerthantheglasstransitiontemperature(Tg)for1h.Microstructureandpropertiesofas-castandannealedsampleswerestudied.Crystallizationphases(Cu10Zr7andCuZr)wereobservedinannealedsamples,andthespeciesandfractionofthesephasesincreasedwithincreasingannealingtemperature.Mic...