简介：Tomeettheincreasingdemandforadvancedmaterialscapableofoperationover2000℃forfuturethermalprotectionsystemsapplication,C/C—ZrC—SiCcompositeswerefabricatedbyreactivemeltinfiltration(RMI)withZr,Simixedpowdersasrawmaterials.ThestructuralevolutionandformationmechanismoftheC/C—ZrC-SiCcompositeswerediscussed,andthemechanicalpropertyoftheas-preparedmaterialwasinvestigatedbycompressiontest.TheresultsshowedthataftertheRMIprocess,aspecialstructurewithZrC-SiCmulti-coatingasouterlayerandZrC-SiC-PyCceramicsasinnermatrixwasformed.ZrCandSiCrichareaswereformedinthecompositesandonthecoatingsurfaceduetotheformationofZr-SiintermetalliccompoundsintheRMIprocess.MechanicaltestsshowedthattheaveragecompressionstrengthoftheC/C-ZrC-SiCcompositeswas133.86MPa,andthecarbonfibersinthecompositeswerenotseriouslydamagedaftertheRMIprocess.

简介：Thecomplexnatureoflaser-materialinteractioncausesnon-stoichiometricablationofalloysamples.Thisisattributedtomatrixeffect,whichreducesanalyzingcapability.Toaddressthisissue,theanalyticalperformanceofthreedifferentnormalizationmethods,namelynormalizationwithbackground,internalnormalizationandthreepointsmoothingtechniquesatdifferentparametersettingsisstudiedforquantificationofAgandZnbyLaserinducedbreakdownspectroscopy(LIBS).TheLIBSspectraoffiveknownconcentrationofsilverzincbinarycompositeshavebeeninvestigatedatvariouslaserirradiances(LIs).CalibrationcurvesforbothAg(I)line(4d^105s^2S1/2→4d^105p^2P1/2at338.28nm)andZn(I)line(4s5s^3S1→4s4p^3P2at481.053nm)havebeendeterminedatLIof5.86×10^10Wcm^-2.SlopesofthesecalibrationcurvesprovidethevaluationofmatrixeffectintheAg–Zncomposites.Withcarefulsamplepreparationandnormalizationaftersmoothingatoptimumparametersetting(OPS),theminimizationofsamplematrixeffecthasbeensuccessfullyachieved.AgoodlinearityhasbeenobtainedinAgandZncalibrationcurveatOPSwhennormalizedthewholeareaofspectrumaftersmoothingandtheobtainedcoefficientsofdeterminationvalueswereR^2=0.995and0.998closerto1.Theresultsofmatrixeffecthavebeenfurtherverifiedbyanalysisofplasmaparameters.BothplasmaparametersshowednochangewithvaryingconcentrationatOPS.However,athighconcentrationofAg,theobservedsignificantchangesinbothplasmaparametersatcommonparametersettingPS-1andPS-2werethegestureofmatrixeffect.Inourcase,thebetteranalyticalresultswereobtainedatsmoothingfunctionwithoptimizedparametersettingthatindicatesitismoreefficientthannormalizationwithbackgroundandinternalnormalizationmethod.

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简介：Semi-solidAl2Y/AZ91magnesiummatrixcompositesslurrywaspreparedbyultrasonicvibration,effectofultrasonicvibrationtemperatureandtimeonmicrostructureofsemi-solidslurrywasinvestigated.Theresultsshowedthatwiththeultrasonicvibrationtemperaturedecreasingthesolidvolumefractionofsemi-solidslurryincreased.Thebestultrasonicvibrationtemperaturewas600oC.Withtheincreaseofultrasonicvibrationtime,theaveragegraindiameterofprimaryа-Mgparticlesdecreasedfirstly,thenincreased,theaverageshapefactorincreasedgraduallyanddecreasedslightlyafter90s,andafewrosettedendriteswereobservedafter120s.Thebestsemi-solidslurrywithaveragegraindiameterof75μmandshapefactorof0.7weregainedafterthemeltwastreatedbyultrasonicvibrationforabout60satnearliquidustemperature(600oC).Atlast,themicrostructureevolutionmechanismofsemi-solidmagnesiummatrixcompositesslurrywasanalyzedbythetheoriesofthermodynamicsandkinetics.

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简介：Mgx(Ti0.9Zr0.2Mn1.5Cr0.3)(x=20%，30%，40%)(集体部分)合成粉末被反应的球milling与氢和他们的氢存储性质准备，微观结构被XRD，SEM和pressure-composition-temperature调查测量。结果证明composites在553K和好加氢动力学有3.83%-5.07%氢能力，甚至在房间温度。在他们之中，milledMg-30%(Ti0.9Zr0.2Mn1.5Cr0.3)合成当它能快速在373K吸收2.1%氢，有最高的加氢动力学，3.5%在在473K的2000s，在3MPa氢压力下面在553K在60s弄平3.26%。改进加氢性质来自粒子在Mg粒子的表面上一致地驱散的Ti0.9Zr0.2Mn1.5Cr0.3的催化效果。

简介：TheinteractionbetweenZn-AleutecticalloyandAl2O3p/6061Alcompositesinthevacuumfurnacewasinvestigated.Greatattentionhasbeenpaidtotheelementsdiffusion,themicrostructureandformationoftheinterfacebetweenZn-AIeutecticalloyandAl2O3p/6061Alcomposites.ExperimentalresultsshowthatZn-AleutecticalloyhasagoodwettingabilitytoAl2O3p/6061Alcompositesandthewettingangledecreaseswithincreasingthetemperatureinvacuum.Aftertheinteraction,aninteractionlayerformsbetweenZn-AIalloyandAl2O3p/6061Alcomposites.Thephasesintheinteractionlayermainlyconsistofα-Al(Zn),Al2O3andCuZn5resultedfromthediffusionofelementsfromtheZn-Alalloy.SeveralporositiesdistributeintheregionneartheinterfaceoftheZn-Alalloy/interactionlayer.TheamountofshrinkagevoidsintheinteractinglayerisrelevanttothepenetrationofZnelementintoAl2O3p/6061Alcompositeswhichisafunctionoftemperature.SoitisnecessarytolowerheatingtemperatureinordertolimittheZnpenetration.

简介：Reactionsintereddensezirconia-mullitecompositeswerepreparedbyisostaticallypressingfromzirconflourandreactivealuminawithdifferentproportionsofTiO2andCr2O3additives.Thepressedcompactsweresinteredatdifferentelevatedtemperatureswithvariablesoakingtimes.Microstructuresandphasedevelopmentinthesinteredcompactswereanalysedtoassesstheinfluenceoftheadditivesonthepropertiesofthezirconiamullitecomposite.

简介：Inthisstudy,C_f/AlcompositesandTiAlalloyswerejoinedbyanewmethodnamedlaser-ignitedselfpropagatingsynthesis(SHS).Mixedpowdersof63.0Ni-31.9Al-5.1Ti(wt%)wereusedasjoininginterlayer.Perfectjointwasgot.ThemicrostructureevolutionandformationmechanismoftheSHSjointwereinvestigatedbyscanningelectronmicroscopy(SEM),energy-dispersivespectroscopy(EDS)andX-raydiffraction(XRD).Resultsshowthatlocalizedmeltingoccursonbothsides.Oneγ-Ni_(0.35)Al_(0.30)Ti_(0.35)andtwoNi-Alreactionlayersform,respectively,intheTiAl/interlayerandC_f/Al/interlayerinterfaces.ThecombustionofNi-Al-TiinterlayerbeginswiththesharpreactionofNiandAl.TheinterlayerproductisaeutecticorganizationofNiAlandAl-richγ.

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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：Si_3N_4-Si_2N_2Ocomposites被液相sintering(LPS)与非结晶的缩放nano的氮化矽粉末制作。Si_2N_2O阶段被in-situreaction2Si_3N_4(s)+1.5O_2(g)=3Si_2N_2O+N_2(g)产生直到在体积的60percent的Si_2N_2O阶段的内容在1650t的sintering温度被获得并且当sintering温度增加了或减少时，减少了，显示反应是可逆的。集体损失，相对密度和平均谷物尺寸与增加sintering温度增加了。当sintering温度在1700degC下面时，Theaverage谷物尺寸是不到500nm。Thesintering过程包含复杂结晶化和阶段转变：非结晶的氮化矽->equiaxialalpha-Si_3N_4->equiaxial->Si_3N_4->杆--相似Si_2N_2O->像针的beta-Si_3N_4。小回合--塑造的beta-Si_3N_4粒子在Si_2N_2O谷物被骗诱，界定差错的高密度位于在1650degC的sintering温度的Si_2N_2O谷物的中间。坚韧在1600degCto7.2MPa从3.5Mpa中心点m~(1/2)增加了在1800degC的中心点m~(1/2)。坚硬在1600degC象21.5GPa(Vickers)一样高。

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简介：Inpursuingexcellentsupercapacitorelectrodes,wedesignedaseriesofM0S2/C0S2compositesconsistingofflower-likedMoS2andoctahedron-shapedCoS2throughafacileone-stephydrothermalmethodandinvestigatedtheelectrochemicalperformanceofthesampleswithvarioushydrothermaltime.Duetothecouplingoftwometalspeciesandabigamountofwell-developedCoS2andMoS2,theresultsindicatedthattheMoS2/CoS2compositeselectrodesexhibitedthebestelectrochemicalperfor-mancewithalargespecificcapacitanceof490F/gat2mV/sor400F/gat10A/gamongallsamplesasthehydrothermaltimereached48h(MCS48).Furthermore,theretentionofMCS48is93.1%after10000cyclesat10A/g,whichmanifeststheexcellentcyclingstability.TheoutstandingelectrochemicalperformanceofMCS48indicatesthatitcouldbeaverypromisingandnovelenergystoragematerialforsupercapacitorsinthefuture.

简介：超离频分子的重量聚乙烯(UHMWPE)纤维/环氧基树脂composites被真空制作处理技术的灌输的帮助树脂(VARI)。composites的治好的条件在80的痊愈温度

简介：AseriesofCd1-xZnxS/K2La2Ti3O10compositesweresynthesizedviaasimpleco-precipitationmethod.ThepreparedsampleswerecharacterizedbyX-raydiffraction（XRD）,scanningelectronmicroscopy（SEM）,X-rayenergydispersivespectroscopy（EDX）,ultraviolet-visiblediffusereflection（UV-Vis）,X-rayphotoelectronspectroscopy（XPS）andphotoluminescence（PL）measurements.ThecompositestructuresconsistedofCd1-xZnxSnanoparticlesevenlydistributedonthesurfaceofK2La2Ti3O10.TheabsorptionedgeofK2La2Ti3O10shiftedtothevisiblelightregionuponintroductionoftheCd1-xZnxSnanoparticles.Thephotocatalyticactivitiesofthecatalystswereevaluatedbyhydrogenproductionundervisiblelightirradiation.ThepreparedCd0.8Zn0.2S（30wt%）/K2La2Ti3O10exhibitedhigherphotocatalyticactivity,evolving6.92mmol/gH2undervisiblelightirradiationfor3h.ThepromotedphotocatalyticactivityofthecompositeswasattributedtothesynergisticeffectbetweenCd1-xZnxSandK2La2Ti3O10,whichresultedinenhancedseparationofphotogeneratedelectronsandholes.