简介:基于刚性配体2-(4-噻唑基)苯并咪唑和二价金属铜离子在水热条件下成功地合成了2个Keggin型多酸化合物[CuⅡ(L1)2(H2O)]2[SiW12O40](1)和[(L1)4(L2)2(H3PMo12O40)2]·5H2O(2)(L1=2-(4-噻唑基)苯并咪唑,L2=苯并咪唑).通过单晶X-射线、红外光谱和元素分析对化合物1和2进行了表征.在化合物1中,存在2个独立的结构单元:Keggin型多酸和蝴蝶状的络合物阳离子[Cu(L1)2(H2O)]2+.化合物2为含有混合配体的超分子结构,由Keggin型多酸、4个游离的L1和2个L2配体组成.此外,研究了化合物1和2的电化学和光催化性能.
简介:采用溶液法合成了一个新颖的离子对化合物[4-BrBz-1-APy]2[Cu(mnt)2](1)(4-BrBz-1-APy=4-Br-(benzylideneamino)pyridinium,mnt2-=马来二氰基二硫烯),单晶衍射结果表明化合物1属于单斜晶系,空间群为P2,/n,晶体不对称单元含1个[Cu(mnt)2]2-阴离子以及2个[4-BrBz-1-APy]]’阳离子.在[Cu(mnt)2]2-阴离子中,Cu离子呈现平面正方形配位几何构型,两个晶体学不等价的4-BrBz-1·Apy+阳离子呈近似平面结构.沿晶体b-轴方向,[Cu(rant)2]2-阴离子(A)与4-BrBz-1-Apy+阳离子(C)以ACCACC的方式交替排列形成混合堆积柱.在化舍物1晶体中,阳离子苯环与阴离子mnt2-配体-CN之间形成了三中心型的非典型氢键.
简介:采用固载化的方法,以环氧氯丙烷做为连接剂,在碱性介质中将β-环糊精接枝到木质素上,制备了木质素基β-环糊精醚(简称L-β-CD)新型吸附剂。采用红外光谱对其结构进行定性分析,通过单因素实验,考察了β-环糊精用量、氛氧化钠用量、反应温度和反应时间对β-环糊精含量的影响,研究了L-β-CD对Cu^2+的吸附性能。结果表明,L-β-CD的较佳合成条件为:β-环糊精与木质素的质量比为3:1,氧氧化钠(质量分数16.7%)用量25mL/g木质素,反应温度55℃,反应时间3h,此时木质素基β-环糊精醚中β-环糊精的含量最大,为30.88μmol/g。20℃时,L-β-CD对Cu^2+吸附容量为16.54mg/g。
简介:TostudytheadsorptionbehaviorofCu+inaqueoussolutiononsemiconductorsurface,theinteractionsofCu+andhydratedCu+cationswiththecleanSi(111)surfacewereinvestigatedviahybriddensityfunctionaltheory(B3LYP)andMller-Plessetsecond-orderperturbation(MP2)method.ThecleanSi(111)surfacewasdescribedwithclustermodels(Si14H17,Si16H20andSi22H21)andafour-siliconlayerslabunderperiodicboundaryconditions.CalculationresultsindicatethatthebondingnatureofadsorptionofCu+onSisurfacecanbeviewedaspartialcova-lentaswellasionicbonding.ThebindingenergiesbetweenhydratedCu+cationsandSi(111)surfacearelarge,suggestingastronginteractionbetweenthem.ThecoordinationnumberofCu+(H2O)nonSi(111)surfacewasfoundtobe4.Asthenumberofwatermoleculesislargerthan5,watermoleculesformahydrogenbondnetwork.Inaqueoussolution,Cu+cationswillsafelyattachtothecleanSi(111)surface.
简介:ThemorphologyandcrystallographyofphasesintheCu-0.12%Zralloywereinvestigatedbyscanningelectronmicroscope(SEM),transmissionelectronmicroscope(TEM),andhigh-resolutiontransmissionelectronmicroscope(HRTEM).Theresultsshowthattheas-castmicrostructureofCu–ZralloyismainlyCumatrixandeutecticstructurewhichconsistofCuandCu5Zrphaseswithafinelamellarstructure.Thedisk-shapedandplatelikedCu5Zrphaseswithfccstructurearefoundinthematrix,inwhichhabitplaneisparallelto{111}aplaneofthematrix.BetweenthecoppermatrixandCu5Zrphase,thereexistsanorientationrelationshipof[112]a||[011]Cu5Zr;(111)a||(111)Cu5Zr.ThespacestructuremodelofCu5Zrphasecanbeestablished.
简介:InordertosuppressthesurfacecrackinginducedbyCuduringreheatingandhotrollingprocess,Cuenrichmentanditsmigrationatthesteel-scaleinterfacewasinvestigatedduringheatingofsteelcastattemperaturesbetween1000℃and1200℃inN2-O2andN7-H2Oatmospheres.ForoxidationofCucontainingsteel,CuenrichedphasewasformedbythepreferentialoxidationofFeandtheenrichmentandmigrationbehaviorofCudependsontheoxidationtemperature,steelchemistryandatmospherecondition.NiinsteelinducedtheformationofsolidCuandNienrichedphaseatsteel/scaleinterfaceandinscalelayerandtheformationofunevensteel/scaleinterface,whichsuppressestheCuenrichmentbecauseofextrusionofCuenrichedregionbeforetheformationofliquidphase.Ontheotherhand,SnadditionpromotestheliquidCuformationatsteel/scaleinterfaceandpenetrationintograinboundaryofCuenrichedphasebydecreasingsolidustemperatureandsolubilitylimit.Inaddition,foroxidationat1200℃,thebehaviorofCuatandaroundthesteel-scaleinterfacewasfounddependenttoalargeextentonmorphologyoftheoxidescaleformedduringoxidation.Attheearlystageofoxidation,Cu-richphaseformedandaccumulatedatthesteelscaleinterfaceunderbothO2-N2andH2O-N2atmospheres.Astheoxidationproceeded,however,Cuenrichmentatanditsmigrationfromthesteel-scaleinterfacewerevastlydifferentfordifferentoxidizingatmospheres.InthecaseofO2-N2oxidation,anoxidelayerformedinitiallyatthesteelsurface,butsoonafteragapwasdevelopedatthesteel-scaleinterfaceandgrewinitssize,whichpracticallyseparatedthescalefromthesteelsubstrate.Thescalelayerformedunderthisconditionwasporous.TheCu-richphaseinitiallyformedattheinterfacewasfoundmigratingtothescalelayer,leavingnoCu-richphaseattheinterface.InthecaseofH2O-N2oxidation,however,thescalelayerformedwasdenseandtightlyattachedtothesteelsurface,andtheCurich-phasecontinuedto
简介:在传统的利用化爆和二级轻气炮作为驱动源的状态方程阻抗匹配实验中,为了考核不同标准材料的可信度,采用了标准材料交叉检验技术。即依次利用这些标准材料作为测量某个待测材料测量雨贡纽线的标准材料,通过比较待测材料雨贡纽线数据的一致性实现对这些标准材料的检验。2004年在神光-Ⅱ装置上完成的二倍频激光Al-Cu和Cu-A1阻抗匹配实验,是一种交叉实验。这两类实验不仅铝、铜二者互为标准材料和待测材料,而且实验包含了正反阻抗匹配两种类型:铝-铜正阻抗匹配实验中冲击波由低阻抗铝进入高阻抗待测材料铜,铜-铝反阻抗匹配实验中冲击波由高阻抗铜进入低阻抗待测材料铝中。
简介:TheroleoftemperatureontheoxidationdynamicsofCu2OonZnO(0001)wasinvestigatedduringtheoxidationofCu(111)/ZnO(0001)byusingoxygenplasmaastheoxidant.AtransitionfromsinglecrystallineCu2O(111)orientationtomicro-zonephaseseparationwithmultipleorientationswasrevealedwhentheoxidationtemperatureincreasedabove300°C.TheexperimentalresultsclearlyshowtheeffectoftheoxidationtemperaturewiththeassistanceofoxygenplasmaonchangingthemorphologyofCu(111)filmandenhancingthelateralnucleationandmigrationabilitiesofcuprousoxides.Averticaltop-downoxidationmodeandalateralmigrationmodelwereproposedtoexplainthedifferentnucleationandgrowthdynamicsofthetemperature-dependentoxidationprocessintheoxidationofCu(111)/ZnO(0001).