简介:AComputationalStudyofGasPhaseChemistryinCarbonNanotubeSynthessbyPECVD;AfieldpointbasedapproachforsensorconditioninginMO-CVDreactors;AMethodforReal-TimeControlofThinFilmCompositionUsingOESandXPS;Amechanism-basedmodelofchemicalvapordepositionofepitaxialSi{sub}(1-x)Ge{sub}xflirts
简介:[篇名]1.55-umsilicon-basedreflection-typewaveguide-integratedthermo-opticswitch,[篇名]120×90ElementThermoelectricInfraredFocalPlaneArraywithPreciselyPatternedAu-blackAbsorber,[篇名]4H-SiCEpitaxialGrowthfcrHigh-PowerDevices,[篇名]A90nmgenerationcopperdualdamascenetechnologywithALDTaNbarrier,[篇名]Acomparativemicrotribologicalinvestigationofdiamond-likecarbonfilmsforapplicationsinmicrosystems,[篇名]Acomparisonofmicrocrystailinesiliconpreparedbyplasma-enhancedchemicalvapordepositionandhot-wirechemicalvapordeposition:electronicanddeviceproperties.
简介:本文在同一条件下分别测试了硫化态的催化剂CoMo/(TiO2-Al2O3)及氨化态的Mo2N催化剂的加氢脱硫和加氢脱氮性能,结果表明,对于噻吩的加氢脱硫反应,硫化态催化剂CoMo/(TiO2-Al2O3)在催化活性及稳定性方面都优于Mo2N,而Mo2N在吡啶的加氢脱氮反应中显示了较大优势.
简介:本文在同一条件下分别测试了硫化态的催化剂CoMo/(TiO2-Al2O3)及氨化态的Mo2N催化剂的加氢脱硫和加氢脱氮性能,结果表明,对于噻吩的加氢脱硫反应,硫化态催化剂CoMo/(TiO2-Al2O3)在催化活性及稳定性方面都优于Mo2N,而Mo2N在吡啶的加氢脱氮反应中显示了较大优势.