简介:采用程序升温氮化的方法制备了钼氮化物催化剂,并用EXAFS方法研究了氮化前后Mo原子的局域配位情况。负载MoO3样品的径向结构函数中有三个峰其中前两个峰对应着最近的Mo-O配位壳层,但是第一个峰与第二个峰的比例比晶体MoO3中的比例大很多,表明分子筛负载的MoO3具有更紧密的结构。氮化以后,Mo2N样品的径向结构函数中有三个峰,对应于一个Mo-N和两个Mo-Mo配位壳层,与面心立方模型符合的很好。根据X射线衍射和EXAFS谱的计算表明,Mo2N中的N原子使Mo-Mo键拉长并削弱。分子筛负载的Mo2N样品具有与非负载Mo2N样品相似的径向结构函数,只是对应于Mo-N壳层的峰较弱,表明负载的MoO3更难氮化。
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.
简介:Ni/Mo2NasaHighlyActiveHydrodenitrogenationCatalystNi/Mo2NasaHighlyActiveHydrodenitrogenationCatalyst¥WenYuZHANG;XinPingWANG;...
简介:Inthiswork,boththethermalexpansionandelectricalconductivityofnanocrystallineLa2Mo2O9werestudied.ThenanocrystallinepowderofLa2Mo2O9wasobtainedbysol-gelmethod,andwiththehelpofSHP(superhighpressure)upto4.5×104atmat700℃forashorttime,andthenanocrystallinepowderwasdensifiedwithoutobviousparticlesizegrowth.TheelectricalconductivityofnanocrystallineLa2Mo2O9wasoneorderofmagnitudelowerthanthatofthemicrocrystallinesampleatthesametemperature.Owingtothephasetransition,themicrocrystallineLa2Mo2O9hasanabruptincreaseofthermalexpansionwithapeakvalueof48×10-6K-1at556℃.Forthenanocrystallinematerial,thepeakvalueincreasesto112×10-6K-1at520℃.Ontheotherhand,above600℃thesignificantgrowthofparticlesizeofthenanocrystallineLa2Mo2O9wasobserved,accompanyingbyatremendousincreaseofthermalexpansionwithapeakvalueofthirdhigherthanthatofLa2Mo2O9.
简介:合成了一种未见报道的标题化合物((C5N2H6)3(C5N2H7)3[(PO4)Mo12O36]·2H2O,Mr=2403.00)并得到单晶,晶体衍射实验发现其属于单斜晶系,P2(1)/n空间群,晶体学参数:a=13.316(3),b=22.414(5),c=20.063(4),α=90.00(4)°,β=100.743(3)°,γ=90.00°,V=5883(2)3,Z=4,Dc=2.713Mg/m3,μ(MoKα)=2.608mm-1,F000=4604,最终R=0.0596,wR=0.1345,GoF=1.042.配体由由簇阴离子[(PO4)Mo12O36]3-之间通过端基氧与2-氨基吡啶形成氢键而相互连接,中间填充了一些水分子及2-氨基吡啶.
简介:ReactionsofCuSCNwithtetramethylthiuramdisulfideinCH3CNinthepresenceofstyreneandN,N,N',N',N'-pentamethyldiethylenetriaminegaverisetoanewcopper(Ⅰ)complexofN,N'-dimethyldithio-cabamate{[Cu(S2CNMe2)]2}n.ThetitlecompoundcrystallizedinthetriclinicP-1spacegroupwithlatticeparametersα=0.7610(4)nm,b=0.8911(4)nm,c=0.9268(5)nm,α=68.66(1)°,β=83.88(2)°,γ=79.31(2)°,V=0.5748(5)nm^3,Z=2.Thecompoundhasaunique1DchainstructurecomposedofCuSCSCuSCSeight-memberedringsandapairofCu-Sbonds,thestructureofwhichhasbeendeterminedbysingle-crystalX-raycrystallography.Theisolationofthiscompoundmayprovidesomehelpfulinformationforthecauseoftheinductionperiodsofthereverseatomtransferradicalpolymerization.
简介:Linearcomplexityandk-errorlinearcomplexityofthestreamcipheraretwoimportantstandardstoscaletherandomicityofkeystreams.Forthe2n-periodicperiodicbinarysequencewithlinearcomplexity2n1andk=2,3,thenumberofsequenceswithgivenk-errorlinearcomplexityandtheexpectedk-errorlinearcomplexityareprovided.Moreover,theproportionofthesequenceswhosek-errorlinearcomplexityisbiggerthantheexpectedvalueisanalyzed.
简介:Twonewdicyanamidecoordinationpolymers,{Mn(dmpz)[N(CN)2]2}2(1)and{Cu(dmpz)[N(CN)2]2}2(2)(dmpz=3,5-dimethylpyrazole),weresynthesizedandcharacterizedbysinglecrystalX-raydiffractionanalysisandIRspectroscopy.In1and2themetalionshavetwodifferentcoordinationmodes,whereoneiscoordinatedtofourdicyanamideanionsandtwomonodentatedmpzmoleculestoformaslightlydistortedoctahedralgeometry,whiletheotheradoptsoctahedralgeometry,surroundedbyfournitrileNatomsandtwoamideNatomsofthedicyanamideanions.Bothcomplexescontaintwoalternatingchainsthatareparalleltoeachother.