简介:Thesinglecrystalofthecomplex[Sc(NO3)3(H2O)2]·(15C5)hasbeenpreparedinacetonitrile.Thenewcomplexhasbeencharacterizedbyelementalanalysis,IRspectra,solubilityandmolarconductancemeasurements.ThestructureofthecomplexisdeterminedbysinglecrystalX-raydiffractionanalysis.
简介:Whitelight-emittingYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswithordermorphologyandwellcrystallizationwerehydrothermallysynthesizedat180°C.Themicrostructure,white-lightemission,andlight-emittingmechanismofthepowderswerecarefullystudiedusingX-raydiffractometry,scanningelectronmicroscopyandphotoluminescencespectra.TheexcitationandemissionspectraofthephosphorpowdersindicatedthecoexistenceofefficientenergytransferfromEu~(3+)toDy~(3+)andinefficientenergytransferfromDy~(3+)toEu~(3+)besidestheenergytransferfromVO_4~(3–)toEu~(3+).IncreasingtheEu~(~(3+))concentrationinitiallyenhancedandthenweakenedtheluminescentintensityofDy~(3+).Thewhite-lightemissionsofYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswerebothrelatedtotheenergytransferbetweenVO_4~(3–)andDy~(3+)/Eu~(3+),aswellasbetweenEu~(3+)andDy~(3+).TheinefficientenergytransferfromDy~(3+)toEu~(3+)wasfirstfound.
简介:采用5水平Box-Behnken设计的反应表面方法论(RSM)被用来优化铈(III)的biosorption到动物和植物起源viz的biowaste材料上。对虾甲壳(PC)和玉米风格(CS)。各种各样的过程参数viz。pH(一:3.0–9.0),生物资源剂量(B:0.05–0.35g/L),起始的金属集中(C:50–350mg/L),接触时间(D:2–6h)并且温度(E:20–60°C)为优化被选择。木头转变被盒子艇长阴谋在现在的盒子中建议。低p值<0.0001验证了模型的意义。为PC的218.3mg/g和为CS的180.2mg/g的最大的Ce(III)举起在最佳条件下面被注意。在平衡等温线之中,Freundlich模型被发现是而兰米尔模型证明最好适合在CS上建议铈biosorption的同类的模式,在PC上建议biosorption的一个异构的模式的最好适合的那个。这被扫描电子显微镜学(SEM)进一步证实。运动研究显示出作为位于这个过程下面的现象建议physisorption的伪first顺序模型的更好的适用性。电影散开被博伊德阴谋的非线性建议。热力学的研究证明这个过程吸热、自发。FTIR分析在Ce(III)biosorption期间证实了酰胺,胺,酉同类和主要白酒组的参予的主要参与。EDAX分析在Ce(III)biosorption期间证实了碳组的主要参予。这是Ce(III)biosorption的参数优化上的第一份报告到用可能从水的环境对Ce(III)的恢复有用的5水平Box-Behnken试验性的设计的biowaste材料上。
简介:Reactionof(MeC5H4)3LnwithHOCH2CH2NMe2intetrahydrofuran(THF)givesthenewcomplexes[(MeC5H4)2Ln(μ-OCH2CH2NMe2)]2(Ln=Sm,Y,Nd)withnitrogenfunctionalizedμ-alkoxideligand.ThecomplexeswerecharacterizedbyelementalanalysisandIR,and[(MeC5H4)2Sm(μ-OCH2CH2NMe2)]2wasstructurallycharacterizedbytheX-raydiffractiontobeadimerformedbytwounsymmetricoxygenbridges.ThecomplexhasatricyclicskeletonwiththeadditionaltwoSm-NbondsviaintramolecularcoordinationofOCH2CH2NMe2.ThecoordinationnumberofthecentralmetalSmisnine.Thetitlecomplexesshowgoodcatalyticactivityforring-openingpolymerizationofε-caprolactone.