简介:通过化学沉积法制备Ni-P、Ni-Mo-P单镀层以及与其成分相同的Ni-P/Ni-Mo-P双镀层。采用纳米压痕法和AFM分析测量镀层表面和截面的残余应力,并用电化学法评估镀层在10%HCl溶液中的腐蚀行为,以获得镀层残余应力与腐蚀行为之间的关系。结果表明:Ni-P单镀层和Ni-P/Ni-Mo-P双镀层表现为残余压应力,分别为241和206MPa;Ni-Mo-P单镀层呈现出257MPa的残余拉应力。残余压应力阻止镀层中孔洞的生长,保护镀层的完整性。Ni-P/Ni-Mo-P双镀层比它们的单镀层具有更好的耐蚀性。此外,镀层的应力状态影响其腐蚀形式。
简介:Cr2O3-formingferriticstainlesssteelshavebeenwidelyexploredasintermediatetemperaturesolidoxidefuelcells(SOFCs)interconnects.However,theevaporationofchromiascalemightmigratetoandpoisonthecathode,leadingtodegradationofthecellperformance.Inthisstudy,Ni-Co-Fe-Pcoatingsweredepositedontheferriticstainlesssteelbymeansofacost-effectivetechniqueofelectrolessmethod.Theyareexpectedtobeconvertedinto(Ni,Co,Fe)3O4spinelwithahighelectricalconductivityandCTEmatchwithstainlesssteel,whichcanblocktheevaporationofchromiaformedonsteelsubstrateexposedtothecathodeenvironmentoftheSOFC.TheeffectsofpH,massratioofFeSO4/(FeSO4+NiSO4+CoSO4)andtemperatureofsolutiononthedepositionrate,compositions,surfacemorphologiesandstructuresoftheNi-Co-Fe-Pcoatingswereinvestigated.TheresultsindicatedthatthedepositionrateincreasedwithincreasingpHwhenpHwaslowerthan9andthenreducedwhenpHwashigherthan9.Thedepositionrateincreasedwithincreasingtemperaturewhentemperaturewaslowerthan80℃andthendecreasedwhentemperaturewashigherthan80℃.ThedepositionratedecreasedwiththeincreaseinmassratioofFeSO4/(NiSO4+CoSO4+FeSO4).ThecoatingsconsistedofNi,Co,FeandP.Thephasestructureofthecoatingwasamorphous.
简介:以占空比、脉冲频率、电流密度、镀液温度为优化工艺参数,以镀层表面硬度、结合强度、磨损量、腐蚀速率为综合优化工艺目标,运用改进的TOPSIS法对脉冲电沉积Ni-P-W合金工艺参数进行优化。优化结果为:占空比30%、脉冲频率250Hz、电流密8A/dm2、镀液温度60℃。采用优化工艺参数进行脉冲电沉积Ni-P-W合金与最优试验设计组相比,表面硬度提高了8.14%,结合强度提高了5.32%,磨损量减小了4.26%,腐蚀速率减小了6.25%。
简介:Threetypesofcarbonnano-onions(CNOs)includingNi@CNOs.Fe3C@CNOsandFe0.64Ni0.36@CNOsnanoparticleshavebeensynthesizedbycatalyticdecompositionofmethaneat850℃usingnickel,ironandiron-nickelalloycatalysts.Comparativeandsystematicstudieshavebeencarriedoutonthemorphology,structuralcharacteristicsandgraphiticcrystallinityoftheseCNOsproducts.Furthermore,theelectrochemicalhydrogenstoragepropertiesofthreetypesofCNOshavebeeninvestigated.MeasurementsshowthattheNi@CNOshavethehighestdischargecapacityof387.2mAh/g,coiTespondingtoahydrogenstorageof1.42%.ThiscomparisonstudyshowstheadvantagesofeachcatalystinthegrowthofCNOs.enablingthecontrollablesynthesisandtuningthepropertiesofCNOsbymediatingdifferentmetalsandtheiralloyforusinginthefuelcellsystem.
简介:Metalgrainsinstonymeteoritesarerelativelymovableduringthermalnetamorphism(Wood,1967;XieandWang,1979;Xie,1986).InviewofthefactthattheJilinmeteoriteisthelargestintheworldknownuptonow,itsmainbodyweighing1770kganditstotalvolumeamountingto117×93×84cm^3,ade-tailedinvestigationintosuchahugemeteoritebodywouldundoubtedlyprovideuswithalotofcluesandinformationvaluableinthestudyofthebehaviorofFe-Nimetalduringthermalmetamorphismofmeteorites.OurrecentinvestigationhasrevealedthatduringthermalmetamorphismoftheJilinchondirtefineFe-Nimetalparticlesmigratedeasilybydiffusioninsolidstate,andsubsequentlyaggregatedintometalnodulesabout5-10mminlength,andthelargestnodulewefoundis30mminsize(Photo1).Inthispaperwepresentsomenewresultsofourstudyconcerningthemigra-tionandconcentrationofFe-NimetalintheJilinchondriteonthebasisofop-tical,SEMobservationsandhigh-temperature-highpressureaswellasshockloadingexperiments.
简介:ThepartialoxidationofethanoltohydrogenwasinvestigatedoverNi/Fe/Lacatalystspreparedbytheco-precipitationmethod.TheeffectsofintroductionofLapromoterandthereactiontemperatureonthecatalyticperformancewerestudied.ItwasfoundthattheintroductionofLaintoNi/Fecatalystsishelpfultoincreasetheselectivitytohydrogenandthestabilityofthecatalysts.TheresultsofXRDandXPScharacterizationshowthatthestructureofthecatalystwaschangedduringthereaction.TheexistenceofLaFeO3speciesispossiblythemainreasonoftheincreaseofthecatalyststability.
简介:磁性的元素Fe,公司和Ni的线性热扩大(CLE)的系数用与MATLAB计算相结合的理论模型从试验性的信息被估计。模型参数能精确地被决定,并且估计的数据在对试验性的结果的好同意。便于评价,热扩大的理论被使用把CLE分开成它的无磁性、磁性的部件。对CLE的无磁性的贡献的计算基于MnBi/NdFeB混血儿的修改Grc性质结合的磁铁都逐渐地减少,当混合磁铁的密度几乎线性地改善时。在293-398的一个温度范围?K,混合磁铁的coercivity温度系数从0.59逐渐地改善?%比较。建模和频率与二低角落频率认为压力消除阀门是一个秒顺序系统是合理的试验性的结果表演。PID控制,死了的乐队赔偿控制和鷸?鷸??
简介:ThesolidsolubilityofCe、La、SmandNdinFeorNiatvarioustemperaturewasdeterminedbymeansofadiffusion-couplemethodwiththeaidofanelectronprobemicroanalyzer.Twomethods,namelyareamethodandwholerangemethod,wereproposedfordataprocessinginthepresentpaper.Theprincipleandre-latedproblemsintheexperimentaldeterminationofthesolidsolubilityofrare-earthelementsinFeorNibyuseoftheabovementionedmethodswerealsodiscussed.
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简介:InordertocontrolthesizeanddistributionofthehighconductiveFe2PinLiFePO4/Fe2Pcomposite,twodifferentcoolingrates(Fast:15℃·min-1,Slow:2℃·min-1)wereemployedaftermechanicalalloying.Thedischargecapacityofthefastcooledwas83mAh·g-1andtheslowcooled121mAh·g-1.TheparticlesizeofthesynthesizedpowderwasexaminedbytransmissionelectronmicroscopyanddistributionofFe2Pwascharacterizedusingscanningelectronmicroscopy(SEM).Inaddition,two-stepheattreatmentwascarriedoutforbetterdistributionofFe2P.X-raydiffraction(XRD)andRietveldrefinementrevealthatLiFePO4/Fe2Pcompositeconsistsof95.77%LiFePO4and4.33%ofFe2P.
简介:基于化学镀Ni工艺,研究Sn-3.5Ag-0.5Cu合金在Ni-P(-SiC)镀层/SiCp/Al基体上的润湿行为,分析镀层的显微结构和Sn-3.5Ag-0.5Cu/Ni-P(-SiC)镀层/SiCp/Al体系的润湿和界面行为。结果表明,SiC颗粒均匀地分布在镀层中,且Ni-P(-SiC)镀层与SiCp/Al复合材料之间没有界面反应。Sn-3.5Ag-0.5Cu对Ni-P、Ni-P-3SiC、Ni-P-6SiC和Ni-P-9SiC镀层/SiCp/Al基体对应的最终接触角分别为~19°、29°、43°和113°。在Sn-3.5Ag-0.5Cu/Ni-P-(0,3,6)SiC镀层/SiCp/Al界面处形成含有Cu、Ni、Sn和P的反应层,其主要包含Cu-Ni-Sn和Ni-Sn-P相。此外,熔融的Sn-Ag-Cu合金可以通过Ni-P/SiC界面渗入Ni-P(-SiC)复合镀层与SiCp/Al基体接触。