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.

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简介：TheCurietemperatureof(Nd1-xPrx)2Fe14CoyBcompounds（x=0,0.2,…,1.0andy=O,2,4,6,14）hasbeendeterminedwithACinitialsusceptibilitymeasurement.ItwasfoundthatthevariationsofCurietempera-turewithxisnotlinearfory=0and14,whereasitislinearforothervaluesofy.Thelatticeconstantsof(Nd1-xPrx)2Fet14BweredeterminedbyusingX-raydiffraction.Thelatticeexpansionwasmostlyalongthecaxis,whereasthatalongthea-axisremainedpracticallyzeroforthewholeseries.ItissuggestedthatPratomsmayshowsitepreferenceinR2M14Bcompounds（M=FeorCo）.DuetothesubstitutionofCoforFe.thetendencyofsitepreferenceofPrbecomeslesspronounced,whichmaybeattributedtothedecreaseofdiffer-enceofcrystalelectricfield（CEF）actingonthetworareearthsiteswiththeintroductionofCoorFe.Incon-trasttothatofthePratoms,thesitepreferenceofCoiu（Nd（1-x）Prx）2Fe（14-y）CoyBcompoundsdoesnotdependonthecompositionoftherareearthsublattice（R=NdorPr）.

简介：Anewhardfacingprocess,reactivebrazecoatingprocess(RBCC)wasstudied,and(TiC+Cr3C2)/FecompositecoatingswerepreparedbyRBCCusingcarbon,Cr3C2,iron,ferrochromiumandtitaniumpowderastherawmaterialsinvacuumbrazefurnace.TheresultsshowthatTiCisin-situsynthesizedinthecoatings.ThemethodsofintroducingCr3C2havegreateffectsonthedistributionofTiC.AddingCr3C2directlytotherawmaterialsforcoatings,fineTiCparticlesaggregateintodiscoidsparalleltothecoatingsurface,whereas,in-situsynthesizingCr3C2incoatings,theaggregationsofTiCarelumpish.Duringbrazecoating,Cr3C2particlesdirectlyaddeddissolveandprecipitatetobecomeneedle-shaped.Thecoatingshaveanevenandsmoothsurfaceandarecombinedwiththeirmildsteelsubstratesbyametallurgicalbonding.

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简介：AZr-1.15wt%Cr-0.10wt%Fealloywasbeta-quenchedfrom1050℃toproduceasupersaturatedα′-phase,andthenheatedforvaryingtimesattemperaturesfrom650℃to760℃toprecipitateZr（CrFe）2.Athermoelectricpower（TEP）techniqueandtransmissionelectronmicroscopy（TEM）wereusedtomonitorthisprecipitationprocess.UsingtheJohnson-Mehl-Avramiequation,theTEPresultsandalineregressionmethod,theactivationenergyfordiffusionandthediffusioncoefficientofchromium（andFe）inα-Zrhavebeencalculatedover650℃～760℃.Thetemperaturedependenceofthediffusioncoefficient,DCr/α（cm2/s）isdescribedat650℃～760℃bytherelationshipformula.ThecoarseningoftheZr（CrFe）2particlesshowsat1/2dependenceofmeanparticlesizeonagingtime,t.Suchatimedependenceistypicalofcoarseningwhereatomtransferacrosstheinterfaceisrate-controlling.

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简介：Basedonclustervariationmethod(CVM)andnaturaliterationmethod(NIM),order-disorderphasetransitionintheintercalationcompoundsM1/2TiS2issimulatedbycomputer.Thefavorableconditions,underwhich3a0×a0superstructureisformed,aregiven,andtheresultsareingoodagreementwiththeexperimentsandtheoreticalcalculations.TherelationshipbetweencriticaltemperatureandM-ion-vacancyinteractionparameterislinear.

简介：我们的以前的研究建议氧化还原作用反应独立继续了TiO的特定的暴露的水晶脸<潜水艇class=“a-plus-plus”>2nanoparticles。TiO上的金属或金属氧化物的地点选择的免职<潜水艇class=“a-plus-plus”>特定的暴露的水晶成功地面对的2用唯一的反应性质继续了TiO的表面<潜水艇class=“a-plus-plus”>在photoexcitation下面的2nanoparticles。控制形状的brookite和金红石TiO的photocatalytic活动的显著改进<潜水艇class=“a-plus-plus”>有Fe的修正的2nanorods<啜class=“a-plus-plus”>3+混合物在可见的光下面被观察。TiO的暴露的水晶脸上的水晶脸选择的金属混合物修正<潜水艇class=“a-plus-plus”>有brookite和金红石阶段的2nanorods成功地被准备。Brookite和金红石TiO地点选择的修正与金属混合物准备的2nanorods应该是理想的可见光的应答的TiO因为背电子的显著抑制，2光催化剂从TiO转2到TiO的表面上的氧化金属混合物有brookite或金红石阶段的2nanorod。在这份报纸，暴露的水晶的发展控制脸的TiO<潜水艇class=“a-plus-plus”>有金红石和brookite阶段的2nanorods被描述。获得的金红石和brookiteTiO<潜水艇class=“a-plus-plus”>2nanorod，与锐钛矿罚款粒子(ST-01)的photocatalytic活动相比为有机化合物的降级显示出显著地高的活动，是为在日本的环境清除的最活跃的商业地可得到的光催化剂之一。为控制形态学的金红石和brookiteTiO的可见光的应答的处理的技术<潜水艇class=“a-plus-plus”>由水晶的2nanorodsFe的脸选择的修正<啜class=“a-plus-plus”>3+

简介：polyacrylonitrile(平底锅)上的electrodepositingFe-Cr2O3合成涂层的过程基于碳纤维，它的催化graphitization被学习。有或没有electrodepositedFe-Cr2O3合成涂层的碳纤维是在不同温度对待的热，结构的变化被XRD，拉曼光谱学和SEM描绘。结果显示那Fe-Cr2O3合成涂层在低温度在碳纤维的graphitization上展出重要催化效果。当Fe-Cr2O3-coated碳纤维是时，热对待在1300?慢敳?慣'R湯映扩牥映汥?獡琠敨瀠敲畣獲牯映汯潬敷?祢椠灭敲湧瑡潩?楷桴爠獥湩?潭摬湩?湡?敨瑡琭敲瑡敭瑮楴?楴吗？？

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：基于炉渣结构分子和离子共存理论,建立1273-1733K下的PbO-CaO-SiO2-FeO-Fe2O3渣系氧化铅活度热力学模型,计算PbO活度并绘制等活度曲线,考察炉渣碱度Q、氧化铁比率R和温度T对活度NPbO和活度系数γPbO的影响。结果表明,活度系数γPbO的模型计算值与文献测定值吻合程度高,说明该模型能较好地反映该渣系结构本质;NPbO呈拉乌尔正偏差,且随渣中PbO含量的升高而增大,但受温度的影响不明显;γPbO随Q的升高而增大;对于Q〉0.3的碱性渣,γPbO随R的升高而出现极大值。该研究结果可用于现代炼铅工艺的热力学研究和操作优化。

简介：ＣｕｒｉｅＴｅｍｐｅｒａｔｕｒｅｏｆＡｍｏｒｐｈｏｕｓＦｅＳｉＢａｎｄＦｅＷＳｉＢＡｌｏｙｓＷａｎｇＬｉｎｇｌｉｎｇ，ＺｈａｏＬｉｈｕａ，ＨｕＷａｎｇｙｕ（王玲玲）（赵立华）（胡望宇））ＤｅｐａｒｔｍｅｎｔｏｆＰｈｙｓｉｃｓ，ＨｕｎａｎＵｎ...

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：本文根据相关研究结果和应用情况，评述铁基结合剂的功罪。指出完善铁基结合剂的可行切入点。

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简介：Sinceamorphousalloyshavewiderapplication,theycannotbefabricatedusingtheconventionalcoolingvelocity.ThebarmaterialplasmasprayingisadoptedtofabricateFebaseamorphousalloyinthisinvestigation.Thecrystallizationdegree,microstructure,micro-hardness,composition,crystallizationtemperatureoftheamorphousalloyandtheflyingrulesoftheatomizedparticlesintheprocessoftheplasmasprayaretested.Theresultsshowthatthealloypreparedhasthehighamorphousdegreeandhomogeneousmicrostructure,micro-hardnessandthecrystallizationtemperaturecanreach1187HVand531℃respectively.Theatomizationisverywellduringtheprocessofplasmaspraying;andthereishighthermalgradient,thecoolingvelocityreaches6.07×107K/s.