简介：265m^2烧结机主传动装置的驱动电机与三环减速机集成为一套一次减速驱动装置部件,整体悬挂于二次减速机高速轴上,驱动电机通过三环减速机带动二次减速机实现对烧结机星轮主轴的回转驱动。从2012年至今,三环减速机出现不同程度的损坏。本文主要对三环减速机损坏的原因进行分析,利用修复工艺将其恢复到正常生产使用条件。

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简介：ThephaseandmorphologytransformationduringthehydrothermaltreatingprocessofY2O3wasevaluatedwithX-raydiffcrcnce(XRD),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),particlesizeandspecificsurfaceareadetermination.TheresultsshowedthatthecubicY2O3didnottransferintohexagonalY(OH)3inpurewater.Therefore,purehexagonalY(OH)3withnanotubeandmicrorodmorphologieswereobtainedbyhydrothermaltreatingY2O3at150℃for12hin15mlof2mol/LNaOHsolutionwithandwith-outPVAorPEGItwassuggestedthatthecharacteristicpreferentialgrowthofY(OH)3wasattributedtothestructureanisotropyofhexahedronY(OH)3.TheadditionofPVAorPEGcouldpromotetheformingprocessofnanotubesbyselectiveadsorptionondifferentcrystalplanes,whichalteredthegrowthratealongdifferentdirectionsandresultedinthediffusionlimitofconstructingionsinthecentertopofrods.Finally,Y(OH)3:EuandY2O3:Eunanotubeswerealsosynthesizedbyusingthismethod,andtheirphotoluminescencepropertieswereevaluated.

简介：MeltspinningtechnologywasusedtopreparetheMg2Ni-type(Mg24Ni10Cu2)100–xNdx(x=0,5,10,15,20)alloysinordertoobtainananocrystallineandamorphousstructure.TheeffectsofNdcontentandspinningrateonthestructuresandelectrochemicalhydrogenstorageperformancesofthealloyswereinvestigated.ThestructurecharacterizationsofX-raydiffraction(XRD),transmissionelectronmicroscopy(TEM)andscanningelectronmicroscopy(SEM)linkedwithenergydispersivespectroscopy(EDS)revealedthattheas-spunNd-freealloydisplayedanentirenanocrystallinestructure,whereastheas-spunNd-addedalloysheldananocrystallineandamorphousstructureandthedegreeofamorphizationvisiblyincreasedwiththerisingofNdcontentandspinningrate,suggestingthattheadditionofNdfacilitatedtheglassformingoftheMg2Ni-typealloy.TheelectrochemicalmeasurementsindicatedthattheadditionofNdandmeltspinningimprovedtheelectrochemicalhydrogenstorageperformancesofthealloyssignificantly.Thedischargecapacitiesoftheas-castandspunalloysexhibitedmaximumvalueswhenNdcontentwasx=10,whichwere86.4,200.5,266.3,402.5and452.8mAh/gcorrespondingtothespinningrateof0(As-castwasdefinedasthespinningrateof0m/s),10,20,30and40m/s,respectively.Thecyclestability(S20,thecapacitymaintainrateat20thcycle)oftheas-castalloyalwaysrosewiththeincreasingofNdcontent,andthoseoftheas-spunalloysexhibitedthemaximumvaluesforNdcontentx=10,whichwere77.9%,83.4%89.2%and89.7%,correspondingtothespinningrateof10,20,30and40m/s,respectively.

简介：用溶胶-凝胶法制备镍锌共掺杂Z型锶钴铁氧体Sr3（NiZn）xCo2（1-x）Fe24O41（x=0～0.5）粉末。用X射线衍射（XRD）和扫描电镜（SEM）表征该铁氧体粉末的晶体结构和表面形貌，并测试其室温磁滞回线和室温电阻率。用微波矢量网络分析仪测定该粉末在2～18GHz微波频率范围的复介电常数和复磁导率，根据测量数据计算电磁损耗角正切及微波反射率，分析该材料的微波吸收性能与电磁损耗机理。结果表明：Sr3（NiZn）xCo2（1-x）Fe24O41粉末呈六角片状形貌，晶体结构为Z型，具有良好的软磁特性；x=0.3时该材料的电阻率最低，微波吸收效果最好，在13.5GHz频率的吸收峰为25.1dB，10dB频带宽度为7.7GHz，兼具强的磁损耗和弱的介电损耗。

简介：采用浓HNO3/浓H2SO4混合酸在60℃超声环境下对T300碳纤维进行表面氧化处理，并以其为增强体制备碳纤维/环氧树脂复合材料。利用X射线光电子能谱仪、拉曼光谱仪、扫描电镜、原子力显微镜对表面氧化前后的碳纤维形态与表面化学性质进行表征，研究氧化时间对纤维的表面形貌与表面性质以及碳纤维/环氧树脂基复合材料力学性能的影响。结果表明，氧化初期，碳纤维表面生成S—、N—含氧基团，以及—OH和—C=O；后期形成—COOH，氧化时间为15min时，—COOH的浓度达到最大值。碳纤维/环氧树脂复合材料的强度随混合酸氧化时间延长而不断增强，氧化15min时强度达到峰值，相比于未氧化处理的样品，复合材料层剪切强度从16.3MPa提高到38.8MPa，抗弯强度从148.3MPa提高到379.7MPa。