简介:Sodiumparanitrophenolatedihydrate(NPNa·2H2O)isanexcellentsemiorganicnonlinearoptical(NLO)material,crystallizesbothinwaterandmethanolwithhighdegreeoftransparency.Goodopticalqualitysinglecrystalsofdimensionupto18mmx6mmx3mmareobtainedbyisothermalsolventevaporationtechnique.Thesolubilityofthecrystalindifferentsolventswasmeasuredgravimetrically.ThesinglecrystalsofNPNa·2H2Oshowvariationinphysicalpropertiesandgrowthrateindifferentsolvents.Methanolorethanolsolutionyieldscrystalsofbipyramidalshapewithclearmorphology.However,methanolgrowncrystalisexhibitingimprovedhardnessparametersandpossessesexcellentthermalstabilityascomparedtowatergrowncrystals.TheeffectsofsolventonhardnessparameteralongwiththermalandopticalpropertiesofNPNa·2H2Owasrevealedinthispaper.
简介:Throughmeasuringthecoefficientoflinearexpansion,thestructureandpropertiesoftheLi2O-Al2O3-SiO2lowexpansionglassceramicscontainingB2O3arestudiedbyJRandXRD.ItisshoutnthattheIRmethodisefficientinthestudyoftheglass-ceramicsstructure.Thereisa"Boronabnormality"inthesystemwhichhasanimportantinfluenceonthepropertiesoftheglass-ceramics.
简介:TheantibacterialeffectofcarryingsilverB2O3-SiO2-Na2Oglassmaterialwasstudiedbymeansofantibacterialring,nephelometery,MICvalue,thinfilmattachmentandmicrocalorimetry,respectively.TheexperimentalresultsoffivekindsofantibacterialtestmethodsarealmostidenticalandcanverifythatcarryingsilverB2O3-SiO2-Na2Oglassmaterialexertsanexcellentantibacterialperformance.Antibacterialringandnephelometeryaresimple,quick,buttheprecisionisrestrictive.MICvalue,thinfilmattachmentmethodandmicrocalorimetrycanquantitativelycomparetheantibacterialeffectsoftheantibacterialglassmaterial.Comparedwiththetraditionalmicrobetestmethods,themicrocalorimetrycananalyzetheinhibitingeffectofthecell'sgrowthandmetabolismontheantibacterialglassmaterialbymonitoringthethermaleffectcontinuouslyandautomatically.
简介:SiO2-B2O3-Al2O3-CaO在低sintering温度使契约成玻璃,高力量被讨论。FTIR和XRD分析被用来与铝的不同内容描绘基本使成玻璃的契约的结构。弯曲力量和热扩大系数也被测试。同时,在660光线衍射(XRD)的sintering温度的合成标本的微观结构,扫描电子显微镜(SEM)分析和其它工具。结果证明分别地,钾和磷的溶解率在95.64wt%lessthan的一种谷物尺寸的条件下面是70wt%和93.7wt%0.074公里,9.78gg-1硫磺的酸,0.5gg-1铵氟化物,160桴???瑳畲瑣牵獥椠?慭湩慴湩摥映吗??
简介:hydroxyapatite(哈)涂层在对待H2O2的碳/碳(C/C)上被完成通过热水地对待和在超声的水下面在一个氨答案加热扔的CaHPO4涂层的正式就职合成洗澡。然后,这哈涂层被放在一个NH4F答案并且热水地再对待制作氟化的hydroxyapatite(联邦住房管理局)为在353,373,393和413K的24h的涂层分别地。结构,形态学和HA和联邦住房管理局涂层的化学作文被SEM,XRD,版本和FTIR描绘,并且粘着性和这些联邦住房管理局涂层的化学稳定性被擦伤测试和沉浸测试分别地检验。结果证明同样准备的联邦住房管理局涂层包含了像针或像条纹的晶体,与那些不同HA涂层。作为加氟作用温度玫瑰,FHA涂层的粘着性首先在在353和393K之间的温度从34.8~40.9N增加了,然后在413K减少了到24.2N,当FHA涂层的溶解率稳定地减少了时。为FHA涂层的性质变化的原因被分析涂层的形态学,作文和结构建议。
简介:以便得到TiB2-Al2O3的同质的混合物和协议,一个表面修正方法被用来准备nano规模的杂交Al2O3涂的TiB2粒子。PE蜡粒子是第一到由杂交,然后nano规模Al2O3粒子的TiB2粒子上涂又是涂的到由PE蜡粒子涂的TiB2的表面上。SEM,TEM和版本被用来描绘同样收到的核心/壳粒子和它的协议的微观结构。试验性的结果显示出那粒子规模TiB2和Al2O3的同质的分散能不仅在混合粉末而且在使脱蜡的协议被形成。协议当时是由煤气压的sintering(GPS)的sintered。物件顶端的装饰物产品显示出与参考样品由正常方法制作了作比较的改进技工性质。
简介:用organo听Sn(OC4H9)4作为先锋,钠dodecylsulfonate(SDS)和SDS明胶(SDS-G)象模板复杂,二听二氧化物胶体的粒子被准备由一自己组装方法。两个SnO2产品分别地与SDS-G与SDS和SnO2-C粒子被标记SnO2-B粒子,它在制作相应于SnO2-B和SnO2-C传感器的SnO2煤气的传感器被使用。X光检查衍射(XRD),扫描电子显微镜学(SEM),传播电子显微镜学(TEM)和thermogravimetry和不同热分析(TG/DTA)被用于描述。试验性的结果证明SnO2-B胶体的粒子由mesoporous组成像片的粒子,当SnO2-C粒子主要由球形的粒子组成时。煤气的察觉到大小证明那个SnO2-B传感器执行察觉到反应到所有目标气体的最好,包括H2,C2H5OH和液体石油气体(LPG)。特别地,SnO2-B传感器的察觉到的反应在1000潩獮的集中在H2空气在32点被完成
简介:石墨和ZrB2–SiC的氧化行为修改了石墨合成在1×105Pa空气和0.2×105PaO2。氧化测试在一个感应的加热炉子被进行。这二材料的氧化跟随了线性率法律。在2100°C的石墨和C–ZrB2–SiC的坚定的半径损失率在1×105−2和1.05×10−2%/s>Pa空气,和3.23×10−2和2.21×10在0.2×105−2%/s>PaO2,分别地。ZrB2并且原文如此的加入显著地减少了石墨的氧化率因为在氧化期间在样品表面上形成的氧化物规模在减少暴露的表面区域帮助在下面底层。在有一样的氧的二不同气氛部分压力,石墨和C–ZrB2–SiC在0.2×105PaO2比在1×105Pa空气。氧化为石墨和C–ZrB2–SiC的控制率的步被建议分别地是通过边界层并且通过在氧化物规模的毛孔的氧的里面的散开。一个模型基于散开理论被建立在他们的氧化行为上讨论全部的煤气的压力的效果。
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简介:Theimplantedionrange,thedepthprofileandthefilmsttuctureoftheimplantedlayerwerestudied;thecarrierconcentrationandthemobilityweremeasured;theconductivitymechanismofthefilmimplantedFeintoAl2O3ceramicwasdiscussed.TheconclusionisthattheimplantedFe2+ionsmoveintoAl2O3latticeandreplaceAl3+toformsubs-titutionimpuritiessothattheionimplantedlat-tice,ascomparedwiththeoriginalone,presentsaneffectivenegativechargewhichformsanegativechargecenter.Avacancyisboundarroundit,andanacceptorisintroducedintheforbiddenband.
简介:TiB2ceramicspowderwassynthesizedfromB2O3-TiO2-Mgsystem.TheeffectsofTiB2additionasdiluentonthecombustionsynthesisprocesswereinvestigated.TheresultsofthermodynamiccalculationandexperimentsshowthattheincreaseofTiB2contentrangingfrom0to20wt%canreducetheadiabatictemperatureTadfrom3100Kto2896KandcombustiontemperatureTcfrom2139Kto1621Krespectively.TheparticlesizeandhalfwidthoftheparticledistributionarealsoincreasedwiththeadditionofTiB2increasingfrom0to20wt%.ThecombustionproductisamixtureofTiB2,MgO,andotherintermediatephases.TheleachedproductcontainsmainlyTiB2,TiO2andTiN,anditsoxygencontentis7.77wt%.
简介:TheRamanspectraof3%(molefraction)Y2O3-ZrO2(3Y)areobtainedatdifferenttemperaturefrom77Kto853K.Theresultsshowthat260cm-1Egand460cm-1Egmodesonthespectrashifttowardlowerwavenumberwiththeincreaseoftemperature;meanwhile,thecontinuityoftheHalfWidthatHalfMaximum(HWHM)andwavenumber(frequency)ofRamanbandsarebrokenandt-phaseonlypartiallytransformstom-phaseat523K.Basedontheexperimentalresults,thispaperdiscussesthet-phaselatticevibrationof3YandpresentstheimagesofvibrationdisplacementofsixRaman-activemodesfort-phaseofZrO2.TheanalysisindicatesthattherearediversitiesexistinginthedisplacementoftheatomicvibrationofRaman-activemodesbecauseoftheirdifferentsymmetriesatvarioustemperature,whichleadstothedifferentchangetendenciesofRamanbands.Furthermore,theabruptchangesofsomeRaman-activemodesindicatingtheatomicdisplacementareassumedtobethecondensationsofphononmodesinthet→mphasetransition.