简介：CdSthinfilmsweredepositedbytheionlayergasreaction(ILGAR)method.Structural,chemical,topographicaldevelopmentaswellasopticalandelectricalpropertiesofas-depositedandannealedthinfilmswereinvestigatedbyXRD,SEM,XPS,AFMandUV-VIS.Theresultsshowedthatthethinfilmsareuniform,compactandgoodinadhesiontothesubstrates,andthegrowthofthefilmsis2.8nm/cycle.Theevolutionofstructureundergoesfromthecubicstructuretothehexagonalonewithapreferredorientationalongthe(002)planeafterannealingat673K.AnamountofC,OandClimpuririescanbereducedbyincreasingthedryingtemperatureorbyannealinginN2atmosphere.ItwasfoundthatthebandgapoftheCdSfilmsshiftstohigherwavelengthafterannealingorincreasingfilmthickness.Theelectricalresistivitydecreaseswithincreasingannealingtemperatureandfilmthickness.

简介：重金属包含pickling污泥(PS)是纯洁链钢的工业的副产品之一，它由于包含的铬和镍被认为危险。处理的PS的传统的方法是垃圾堆和水泥团结。这研究针对由团结/稳定处理PS并且作为glassceramics的一个成核代理人再使用它。结晶化行为和在CaOMgOSiO2艾尔2O3系统被把PS看作成核代理人学习。试验性的结果证实那介绍14?glassceramics的成核代理人能减少的wt%PS在110.8的结晶化温度?渠扯摯?猤映潯吗？

简介：Recoveryprocessesofsecondaryresourcesusuallyencounterproblemsbecauseofthediversecompositionsofwastes.Toenhancetheapplicabilityoftraditionalhydrometallurgicalprocesstowardsecondaryresources,theadjustmentofcomponentsisnecessary.Intraditionalhydrometallurgicalseparation,precipitationandcomplexationareextensivelyused.However,theircombinationasaspecificmetalseparationmethodhasnotyetbeenstudiedindetail.Thisapproachisverypromisingforsolvingproblemscausedbychangeablecomponentsduringrecyclingprocessesofsecondaryresources.Thispaperreviewstheeffectsofprecipitationandcomplexationinmetalseparationprocesses,andametalseparationmethodsystemof‘‘complexation–precipitation’’developedtoadjustthecomponentsofsecondaryresourcesisintroduced.

简介：Vanadiumnitridewassynthesizedbyone-stepmethodusingV2O5andcarbonblackasrawmaterialsinnitrogenatmosphere.ThephasesofdifferentreactionproductspreparedindifferentreactiontemperatureswereanalyzedbyX-raydiffraction(XRD),andthedynamicbehavioroftheprocessofsynthesizingvanadiumnitride(VN)byone-stepmethodwasstudiedwithnon-isothermalthermogravimetry.Themechanismfunctionandkineticparametersofreactionprocesswerecalculatedbythermalgravimetricanalyses(TGA),andthereactionrateequationwasestablished.TheXRDresultsshowthatforthesamplestestedwithminimalVNafterholdingfor4hat1273K,themainphaseofproductsisVNat1476K,whilesomevanadiumnitridestransformintovanadiumcarbidesagainover1573K.ItisfoundthatN2isbeneficialtostimulatereductionandproceedcarbonizationreaction,andthereductionandnitridationreactioncanoccursimultaneously.TheactivationenergyofpreparingVNbyone-stepmethodis104.005kJ·mol-1,andthefrequencyfactoris470.52at1280–1358K,and150.052kJ·mol-1and2.359104at1358–1426K,respectively.

简介：为提高对时变信号的分析处理能力，设计了一组同时满足抗混淆、完全重构和正交化的Q—shift滤波器。与传统Q—shift滤波器相比，其权系数可以根据输入信号特性进行自适应调整。将基于自适应Q—shift滤波的双树复小波变换用于对超声缺陷信号进行阈值降噪，实验结果表明，与Q—shift10／10和DWT两种传统方法相比，去噪后信号的信噪比可以分别提高1．03dB和1．97dB。

简介：有bimodal粒子尺寸的钻石/铜composites的热传导性被学习。composites与40和100颗m尺寸钻石的混合物通过液体铜的压力渗入被准备进钻石预先形成。有钻石的不同coarse-to-fine体积比率的预先形成的渗透被调查。有bimodal尺寸分发的钻石/铜composites的热传导性与从Chu开发的一个分析模型导出的理论价值相比。钻石/铜composites能到达更高热的传导性，他们的表面粗糙能被使用bimodal钻石粒子尺寸改进，这被预言。

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：nano石墨表/氧化铝composites被一个灵巧的受精减小过程在situ准备。composites的微观结构被X光检查衍射(XRD)分析，并且在减小以后的最后的阶段作文是艾尔2O3,金属Fe和石墨水晶。扫描电子显微镜学(SEM)图象证明Fe的粒子尺寸是大约20?nm，和石墨的lamellae厚度是大约30?nm。然后，绝缘的性质和composites的传导性的机制在0.01-1.00的频率范围试验性地被调查?由阻抗分析器的GHz。composites的介电常数的真实部分与Fe3+集中增加的结果表演，由于在Fe和艾尔23和薄片状的石墨形成的三维的网络。因此，悦耳的microtopography和nano石墨表/氧化铝composites的电的参数能被改变Fe3+集中认识到。

简介：Thewell-distributionspindleLiFePO4(LFP)nanoparticlesascathodeoflithiumsecondarybatteriesweresynthesizedbyasolvothermalreactionrouteatlowtemperature(180°C)inwhichtheascorbicacidwasusedasreducingagent.InordertoguaranteethatthepHvaluesofthermalsystemswerenotaffectedtoomuchandthereducibilityofthesystemwasenhancedatthesametime,glucosewaschosenasanauxiliaryreductantinthisreaction.TheobtainedpowderswerecharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM),andlaserparticleanalyzer.Theresultsshowthatthecarbon-coateduniformspindleolivineLiFePO4/C-glucoseparticles(glucoseasauxiliaryreductant,LFP/C-G)arepreparedwiththesize500–600nmandwithoutanyimpurityphases.Theirelectrochemicalpropertieswereevaluatedbyelectrochemicalimpedancespectroscopy,cyclicvoltammetry,andgalvanostaticcharge/dischargetests.LFP/C-Ghasahigherconductivityandbetterreversiblecapabilitythancarbon-coatedLFP(LFP/C).ThehighestdischargecapacityofLFP/C-Gis161.3mAh·g-1at0.1Cand108.6mAh·g-1at5.0C,respectively.TheresultsimplythattheneatcrystalnanostructureofLFP/C-Ghasexcellentcapacityretentionandcyclingstability.Theaddingofglucoseisthekeyfactorforthewelldistributionandneatcrystalstructureofnanoparticles,thustheelectrochemicalperformancesofmaterialsareimproved.

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简介：微米大小的Sr2(P2O7):Ce，Tb绿黄磷被与它的先锋在不同温度被退火准备综合了由一同沉淀(NH4)在周围的温度的2HPO4。黄磷的阶段结构，谷物尺寸，表面形态学，和光性质被X光检查衍射调查，扫描电子显微镜，传播电子显微镜，和荧光光谱。先锋的产品在1,100点退火了的结果表演??‰浮???匠??伲?????畅？？

简介：La-dopedSr-hexaferrite(Sr_(1-x)La_xFe_(12)O_(19))(x=0.05,0.10,0.15,0.20)nanopowderswithparticlesizerangingfrom80to110nmweresuccessfullysynthesizedbysol-gelauto-combustion.Thephaseformationtemperatureincreases,whiletheparticlesizedecreasesastheLadopingcontentgoesup.ThepartialsubstitutionofSr~(2+)byLa~(3+)resultsinthesuppressioneffectsonthegrowth-upofthecrystallitesandtheenhancementoftheelectronhoppingbetweenFe~(3+)withdifferentvalences,whichleadstotheimprovementinthedielectriclossandmagneticloss.Therefore,boththemicrowaveabsorbingabilitiesandabsorbingfrequencyrangesaretunedbyLa-doping.ThesynthesizedSr-hexaferritenanopowderswithdopingelementcontentof0.10demonstratethefinebroadmicrowaveabsorbingproperties.

简介：Auniformtransienttemperaturefieldmodelofelectricalcontactsoperationwasfoundbyanalyzingtheprocessofclosingarc→constrictionresistanceJouleheat→breakingarc.EssentialparametersofAg/La2NiO4electricalcontactmaterialfortransienttemperaturefieldcalculationwereobtainedthroughtestsofelectricalcontactexperimentalinstrumentunder18VDCindifferentcurrents,othercorrelationexperiments,andcalculationanalysis.Thefiniteelementmethodwasappliedtosolvethetransienttemperaturefield,andthefeaturesanddistributionofthetransienttemperaturefieldwereobtained.Theconditionofmaterialerosionandmasstransfercanbeforecastedbythosecalculationresults.ItisbeneficialtoresearchaboutthelifetimeofAg/La2NiO4electricalmaterial.

简介：EmployingLi2CO3,NiO,Co3O4,andMnCO3powdersasstartingmaterials,Li[Ni1/3Co1/3Mn1/3]O2wassynthesizedbysolid-statereactionmethod.Variousgrindingaidswereappliedduringmillinginordertooptimizethesynthesisprocess.Aftersuccessiveheattreatmentsat650and950℃,thepreparedpowderswerecharacterizedbyX-raydiffraction(XRD)analysis,scanningelectronmicroscopy,andtransmissionelectronmicroscopy.Thepowderspreparedbyaddingsalt(NaCl)asgrindingaidexhibitaclearR3mlayerstructure.ThepowdersbyothergrindingaidslikeheptaneshowsomeimpuritypeaksintheXRDpattern.Theformerpowdersshowauniformparticlesizedistributionoflessthan1μmaveragesizewhilethelattershowsawidedistributionrangingfrom1to10μm.EnergydispersiveX-ray(EDX)analysissshowthattheratioofNi,Co,andMncontentinthepowderisapproximately1/3,1/3,and1/3,respecively.TheEDXdataindicatenoincorporationofsodiumorchlorineintothepowders.Charge-dischargetestsgaveaninitialdischargecapacityof160mAh·g-1forthepowderswithNaCladditionwhile70mAh·g-1forthepowderswithheptane.