简介：

简介：3-degree-of-freedom(3-DOF)的一个新分析模型旋转罗盘加速表系统由一个1-DOF驱动器和2-DOF感觉模式组成被介绍。模型构造微分方程由向量分析与系统的每DOF联系了的lumped。因此建立的联合微分方程是为他们在时间和频率领域的回答的解决的经分解。就这些频率反应方程而言，新奇设备设计概念被强迫感觉阶段到零导出，它导致在结构的频率之间的某个关系，从而在系统的表演上引起抑制效果的最小化。而且，现在的旋转罗盘加速表结构的可行性在他们的事件为旋转罗盘行动和线性加速的察觉用一个唯一的差别对待的计划被学习。这个计划把旋转罗盘加速表的提出的解决的短暂解决方案与同步解调和过滤的进程相结合，它导致同相并且系统输出的照部件发信号。这二个部件能在尖运动和线性加速的察觉被利用。获得的分析结果被模拟在MATLAB/Simulink环境验证，并且结果在对对方的优秀同意，这被发现。

简介：传统地形辅助导航适配区选择主要根据某一个地形特征参数的大小决定,因此不可避免地存在对地形适配性评判的不全面性。为了克服传统方法的缺点,提出了一种基于熵值法赋权灰色关联决策的地形辅助导航适配区选择方法,该方法综合考虑了地形标准差、粗糙度、地形高度熵及相关系数对适配区选择的影响。首先,利用计算得到的各特征参数值构建灰色决策矩阵;其次,对决策矩阵进行极差变换以及归一化处理得到灰色关联判断矩阵;最后,采用熵值赋权法客观计算各决策属性的权重,得到地形适配性综合评价指标。仿真结果表明,在评价值高的区域进行地形辅助导航,其匹配误差将更小。

简介：Perovskite-typeLa1-xCexMnO3（x=0-10%）catalystswerepreparedbyflamespraypyrolysisandtheiractivitiesduringthecatalyticoxidationofbenzenewereexaminedoverthetemperaturerangeof100-450℃.ThestructuralpropertiesandreducibilityofthesematerialswerealsocharacterizedbyX-raydiffraction（XRD）,N2adsorption/desorption,H2temperature-programmedreduction（H2-TPR）andX-rayphotoelectronspectroscopy（XPS）.TheincorporationofCewasfoundtoimprovethebenzeneoxidationactivity,andtheperovskiteinwhichxwas0.1exhibitedthehighestactivity.Phasecompositionandsurfaceelementalanalysesindicatedthatnon-stoichiometriccompoundswerepresent.TheincorporationofCehadanegligibleeffectonthespecificsurfaceareaoftheperovskitesandhencethisfactorhaslittleimpactonthecatalyticactivity.IntroductionofCe44+resultedinmodificationofthechemicalstatesofbothB-siteionsandoxygenspeciesandfacilitatedthereducibilityoftheperovskite.ThesurfaceMn4+/Mn3+ratiowasincreasedasaresultofCe4+substitution,whileadecreaseinthesurface-adsorbedO/latticeO(Oads/Olatt)ratiowasobserved.Therelationshipbetweenthesurfaceelementalratiosandcatalyticactivitywasestablishedtoallowabetterunderstandingoftheprocessbywhichbenzeneisoxidizedoverperovskites.

简介：Nanostructuredtransitionmetaloxidesarepromisingalternativeanodesforlithiumionbatteries.Li-ionstorageperformanceisexpectedtoimproveifhighpackingdensityenergyparticlesareavailable.Herein,Mn2O3microsphereswithaca.18μmdiameterandatappeddensityof1.33g/cm3weresynthesizedbyafacilesolvothermal-thermalcoversionroute.SphericalMnCO3precursorswereobtainedthroughsolvothermaltreatmentandtheydecomposedandconvertedintoMn2O3microspheresatanannealingtemperatureof700C.TheMn2O3microspheresconsistedofMn2O3nanoparticleswithanaverage40nmdiameter.TheseporousMn2O3microspheresallowgoodelectrolytepenetrationandprovideanionbufferreservoirtoensureaconstantelectrolytesupply.TheMn2O3microsphereshavereversiblecapacitiesof590and320mAh/gat50and400mA/g,respectively.Wethusreportanefficientrouteforthefabricationofenergyparticlesforadvancedenergystorage.

简介：PureAl2O3-2SiO2powderswerepreparedbysol-gelandcoprecipitationmethods,andtheiralkaliactivationreactivitieswerecompared.Thealkali-activationreactivityofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbythecoprecipitationmethod.Thepowderswereinvestigatedby27AIand29Simagic-anglespinningnuclearmagneticresonancespectroscopy（MASNMR）tounderstandtherelationshipbetweentheirstructureandalkali-activationreactivity.The27AlMASNMRdatashowedthatthefive-coordinateAIcontentofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbycoprecipitation.Thehighercontentoffive-coordinateAlcorrespondedtohigheralkali-activationreactivity.The29SiMASNMRdatashowedthatforthepowderpreparedbythesol-gelmethod,siliconwasreplacedbyaluminumatsecondarycoordinationsitesofthecentralSiatomsduringcalcination.However,forthepowderpreparedbysingle-batchcoprecipitation,themainchangewasfromalowdegreeofpolycondensationtoahighdegreeofpolycondensation.