首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献,搜索用时 784 毫秒
1.
以1-苯基-3-甲基-4-苯甲酰基吡唑啉酮-5(HPMBP)为第一配体,茚三酮(Nin)为第二配体,合成了三种未见文献报道具有组成为Ln(PMBP)_3·Nin·3H_2O(Ln=La、Nd、Gd)的稀土配合物。用元素分析、摩尔电导、紫外可见光谱、红外光谱、差热-热重谱、 ̄1H核磁共振谱和x-射线粉末衍射对配合物进行了表征。  相似文献   

2.
利用循环伏安和极谱研究了Keggin结构钼钨硅杂多酸H4SiMo12-nWnO40(记为SiMo12-nWn,n=2,4,6,8,10)及其稀土衍生物K10H3〔Ln(SiMo6W5O39)2〕(记为Ln(SiMo6W5)2,Ln=La3+,Ce3+,Pr3+,Nd3+,Sm3+,Eu3+,Gd3+,Dy3+,Yb3+)在水溶液中的氧化还原性质,讨论了取代原子和酸度对杂多阴离子氧化还原性质的影响,探讨了极谱半波电位与pH的关系,并根据静电模型对杂多配合物的氧化还原规律性给予了合理的说明。  相似文献   

3.
古国榜  杜冰 《化工冶金》1997,18(2):115-118
对MNA-TBP从盐酸介质中萃取Ir(Ⅳ)作了研究。结果表明:MNA-TBP对Ir(Ⅳ)萃取有协同效应。当MNA和TBP在正辛烷中的浓度各为0.45mol/L,待萃液中HCl总浓度为4mol/L,铱浓度为173.13μg/ml,相比为1时,协萃系数R为2.33,协萃合物的组成为(MNAH)^+.IrCl6^2-.(HTBP)^+。  相似文献   

4.
本文采用HNO3和H2O2溶解试样,在8mol/LHNO3介质中,以溴酸钾将Ce(Ⅱ)氧化成Ce(Ⅳ)继以P204/CCl4萃取Ce(Ⅳ),将三价稀土元素与四个铈分离,用ICP-AES法测定CeO2标准物质中La,Pr,Nd,Sm,Gd和Y,分析结果均落在标准值的置信区间内RSD〈6%。  相似文献   

5.
研究了微量碱土金属镁、钙、锶、钡与PMBP-TBP形成萃合物,其摩尔比为Sr:PMBP:TBb=1:2:2。在pH8.O时用PMBP-TBP协同萃取Sr(Ⅱ),用盐酸反萃后由ICP-AES法测定。该方法使锶的检出限达到10 ̄(-4)μg/ml,应用于样品分析中,得到了满意的结果。  相似文献   

6.
本文采用HNO3和H2O2溶解试样,在8mol/LHNO3介质中,以溴酸钾将Ce(Ⅲ)氧化成Ce(Ⅳ),继以P204/CCl4萃取Ce(Ⅳ),将三价稀土元素与四价铈分离,用ICP-AES法测定CeO2标准物质中La、Pr、Nd、Sm、Gd和Y,分析结果均落在标准值的置信区间内,RSD<6%。  相似文献   

7.
镧系元素高氯酸盐苯丁基亚砜配合物的合成与表征   总被引:7,自引:0,他引:7  
本文以稀土高氯酸盐RE(ClO_4)_3nH_2O(RE=La~(3+)、Ce~(3+)、Pr~(3+)、Nd~(3-)、Sm~(3-)、Eu(3+),n=6~7)与苯丁基亚砜PBSO(C_6H_5C_4H_9)在无水乙醇体系中合成出六个新配合物,并对配合物进行了元素分析,稀土离子含量测定,配体PBSO含量测定ClO_4~-含量测定、IR谱、导电、TG-DTA分析及X-射线粉末衍射。确定了配合物的组成为[RE(BPSO)_7(ClO_4)](ClO_4)_2,配位数为8,电解质类型为1:2。  相似文献   

8.
对稀土气态配合物LnAl3Cl12的稳定性进行线性分析,发现其稳定常数的对数值,与镧系离子势(Z+/r)之间存在线性关系,将镧系稀土分为两组,La-Gd和Tb-Lu;与镧系离子基态角量子数存在斜W效应,将镧系稀土分为四组,La-Nd,Pm-Gd,Tb-Ho,Er-Lu。在每一组内,LnAl3Cl12的稳定常数呈线性变化  相似文献   

9.
t-BAMBP萃取铷、铯反应机理及热力学函数研究   总被引:5,自引:1,他引:4  
研究了t-BAMBP(简称ROH)从碱性水相中萃取铷、铯的机理。以斜率法、饱和法测定萃合物组成为MOR·3ROH(M表示Rb ̄+、Cs ̄+)。ROH萃取铷、铯为阳离子交换机理,萃取方程式为+2(ROH)_2(MOR·3ROH)。由温度效应按lgD-T ̄(-1)的直线斜率,求得萃取热焓△H,由△H和表观萃取平衡常数K便可计算自由能△G和熵变△S。萃取铷、铯的过程是一个放热反应  相似文献   

10.
采用HNO_3和H_2O_2一溶解试样,在8mol/LHNO_3介质中,以溴酸钾将Ce(Ⅲ)氧化成Ce(Ⅳ),继以P204/CCl_4萃取Ce(Ⅳ),将三价稀土元素与四价体分离,用ICP—AES法测定CeO_2标准物质中La,Pr.Nd,Sm,Gd和Y,分析结果均落在标准值的置信区问内,RSD<6%.  相似文献   

11.
张安运 《稀土》2001,22(1):1-4
研究了1,2-双(1′-苯基-3′-甲基-5′-氧代吡唑-4′-基)乙二酮-[1,2](H  相似文献   

12.
Coordination chemistry of rare earth with Schiffbase has developed rapidly in the last fewyears ,butthe majority of the complexes studied are derivedfromaromatic Schiff base .So far less papers of rare earthcomplex with aliphatic Schiff base have been rep…  相似文献   

13.
The structures of crystalline (over a wide temperature range) and molten rare-earth metal-LnCl3 (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy) trichlorides are comprehensively studied by Raman spectroscopy.  相似文献   

14.
PreparationandCharacterizationofHeteropolytungstoarsenateComplexesContainingLanthanideElements¥WangWeiqing(DepartmentofChemic...  相似文献   

15.
Themetalcomplexesofhydrazideshaveattractedconsiderableinterestowingtotheirantifungalandantibacterialactivities[1 ,2 ] .Theycanalsobeusedasanalyticalreagents[3 ]andextractingagentsformetalsalts[4 ] .Manycomplexesofhydrazideshavebeensynthesizedandcharacterized[5]…  相似文献   

16.
《Hydrometallurgy》2007,89(1-4):210-215
In this paper, solvent extraction of Pr (III) and Nd (III) using 8-hydroxyquinoline in chloride-acetate medium has been systematically investigated. The effect of various parameters, such as equilibrium time, aqueous pH, extractant concentration, acetate ion concentration, chloride ion concentration, and organic solvent, on the extraction has been discussed. The synergistic effect in the mixtures of 8-hydroxyquinoline (HQ) and 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester (P507) has been explored, and the largest synergistic enhancement factor has been calculated. The separations of Pr (III), Nd (III) and La (III) by 8-hydroquiloline alone and by mixtures of HQ and P507 have been studied, and the results demonstrate that it is possible to separate Pr (III), Nd (III) and La (III) with the mixtures of HQ and P507. At last, the stripping of Pr, Nd and La (III) has been performed.  相似文献   

17.
双水杨醛1,6-己二胺希夫碱轻稀土配合物的合成和表征   总被引:4,自引:0,他引:4  
合成并表征了双水杨醛缩 1,6 己二胺希夫碱配体 (C2 0 H2 4 N2 O2 ,以L表示 )与轻稀土Ln3 的 7种新的固体配合物 [LnL2 ](NO3) 3(Ln =La、Ce、Pr、Nd、Sm、Eu、Gd)。利用元素分析、摩尔电导、红外光谱、电子光谱、X射线衍射物相分析、热分析方法进行表征。中心金属离子Ln3 与希夫碱配体中的亚胺氮和酚羟基中的氧发生配位 ,配位数为 8。  相似文献   

18.
A novel Schiff base N′-[1-(3-aminophenyl)ethylidine]isonicotinohydrazide was prepared and its complexation behavior towards some selected lanthanides had been studied employing pH-metric and calorimetric titration and spectral techniques. pH-metric studies were carried out for the trivalent La, Pr, Nd, Sm, Eu, and Gd complexes in 30% aqueous-dioxane medium at constant ionic strength of 0.05 mol/L NaClO4 and at different temperatures of 293, 303 and 313 K. The proton-ligand formation constants of the ligand indicated the presence of only one dissociable proton while the metal-ligand formation constants were compatible with the formation of 1:1 Ln(Ⅲ) complexes. The sta-bility of the complexes followed the order: La3+Gd3+, showing a break at gadolinium. The thermodynamic parame-ters, ΔG, ΔH and ΔS associated with protonation and complexation reactions were negative which suggested that all reactions were exother-mic and enthalpy-driven. Isothermal calorimetric studies of Gd3+-aeINH systems at 303 K also showed exothermic nature of the complexation reaction and formation of 1:1 complex in agreement with the pH-metric data. Formation of 1:1 complexes was confirmed by the characteriza-tion of Nd(Ⅲ) complex. A seven coordinated geometry was assigned for the complex based on its elemental and spectral data.  相似文献   

19.
Themagneticresonanceimaging (MRI)tech niqueforthemedicineisveryusefultodiagnosepre tumorandbloodvesseldiseaseinheartandbrainandothermalignantpre diseases .Therefore ,specialatten tionhasbeenalsopaidtoMRIcontrastagents ,whichareindispensablediagnosingdrugsforthemagneticresonanceimagingtechnique[1,2 ] .Gadolinium (Ⅲ)complexwithsomepolycarboxylicandpolyaminelig ands ,suchasGd(DTPA)·nH2 O ,waswidelyusedincliniclongago .OurpreviousworkshowsthatsomepolycarboxylicSchiffbasecomplexeswithrareea…  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号