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Nd比值测定中的Sm、Nd分离——HDEHP分离法 总被引:3,自引:0,他引:3
利用一种涂结型阳离子分离交换树脂分离测定Sm-Nd年龄中的Sm、Nd二元素。本文详细介绍了这种方法的基本原理和树脂制备、装柱条件及化学分离过程。并且与测定Sm-Nd同位素年龄中的另一种Sm、Nd元素分离方法(α-羟基异丁酸HBAR分离法)进行了比较。 相似文献
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钇、钕和钐负载的MCM-41介孔材料的合成和表征 总被引:2,自引:0,他引:2
以十六烷基三甲基溴化铵(CTMAB)为模板剂,以正硅酸乙酯(TEOS)为硅源,采用水热晶化法成功合成了Y,Nd,Sm骨架负载的MCM-41介孔材料,通过XRD,N2吸附脱附、SEM,IR,TG-DTA等测试手段对其孔结构、微形貌和Y,Nd,Sm的存在状态进行了表征。XRD结果表明,合成样品具有典型的六方有序排列的MCM-41结构,Y,Nd,Sm离子可以进入介孔材料骨架。N2吸附脱附等温线表明样品具有明显的介孔特征。SEM图片表明各负载样品呈较规则的球形颗粒分布,直径约在0.10~0.15μm。样品的IR图谱在960~985cm-1区间分别出现了Si-O-Ln(Ln=Y,Sm,Nd)的特征吸收峰,证明Y,Nd,Sm存在于介孔材料的骨架中。TG-DTA结果表明,YMCM-41,NdMCM-41和SmMCM-41介孔材料中存在着两种不同的模板剂键合位,进一步证明了Y,Nd,Sm进入了介孔材料骨架。 相似文献
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利用光声振幅谱和位相谱对稀土配合物(Nd(DBM)3、 Sm(DBM)3和Gd(DBM)3分子内弛豫过程进行了研究。Sm(DBM)3、 Gd(DBM)3和Nd(DBM)3的配体π-π*跃迁的光声振幅强度依次增强,而Gd、 Sm和Nd的配合物在配体吸收波段内位相依次减小,反映分子内的弛豫过程。对于Gd(DBM)3,配体最低三重态能量不能传递到中心离子4f激发态能级上而直接弛豫回基态;对于Sm(DBM)3和Nd(DBM)3,配体三重态能量有效地传递到中心离子上, Nd3+各能级间隔小且相互重叠,激发态能量几乎全部以无辐射跃迁回基态; Sm3+为荧光离子,激发态上的部分能量以荧光形式发射。由此并结合荧光光谱的结果建立了分子内能量弛豫模型。 相似文献
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采用溶胶 -凝胶法合成了YAG∶Nd ,Re(Re =Pr,Sm ,Dy)系列化合物 ,研究了它们的光谱性质 .结果表明 :Pr3 + ,Sm3 + ,Dy3 + 对YAG基质中Nd3 + 的发光具有猝灭作用 ,属于有害杂质 ,在激光晶体原料中必须除去 相似文献
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用数学模拟法研究了 NdCl_3-SmCl_3-HCl-H_2O-1.5M 氨化 P507-煤油体系的萃取平衡。提出了采用不氨化和氨化萃取剂的萃取平衡模型。利用这些模型初步进行了分馏萃取模拟,并研究了各种平衡数据之间的相互关系,利用其内在联系提出了较简单的模拟方法,以方便模拟工艺要求的任何氨化率的萃取体系。模拟结果与 Nd-Sm 分离试验结果符合得很好,Nd 和 Sm 产品纯度误差分别为0.13%和1.3%。文中还提出了保证不乳化、进料级位置合理、符合萃取要求的不同 Nd、Sm 组分的优化分离工艺。只用6~7级就可使 Nd、Sm 两种产品纯度达到99%以上。 相似文献
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《Analytical letters》2012,45(1):142-150
We present a precise and accurate method for the determination of 143Nd/144Nd isotope ratio without Nd and Sm separation by multiple collector inductively coupled plasma mass spectrometry. We corrected instrumental mass discrimination by applying the natural constant 146Nd/144Nd ratio as an internal standard after isobaric interference correction of 144Sm on 144Nd using interference-free 147Sm/149Sm ratio for Sm mass fractionation. The present method was validated by duplicate analyses of several certified reference materials after dissolution and cation-exchange resin purification. The precision (2σ) of the 143Nd/144Nd ratio is less than 10 ppm (internal) and 20 ppm (external), respectively. 相似文献
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A pre-irradiation group separation procedure for the quantification of 11 to 13 rare earth elements (REE) in geological materials by neutron activation analysis, with yield determination by mass spectrometry isotope dilution analysis of Sm and Nd, is described. Utilization of the shorterlived isotopes of the REE allow sufficient data for most geochemical studies to be obtained within one day of irradiation, although where necessary additional information may be obtained following a decay period of three to four weeks. Analysis of selected USGS rock standards shows the method to be both accurate and precise. 相似文献
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Anion-exchange chromatography of the rare earth (Sm, Nd, Pr, Ce) ions in methanol-nitric acid-water media is performed using
high-pressure liquid chromatography. The separation method is especially designed for determination of148Nd in the nuclear fuel cycle in order to find precise burn-up values. The high-pressure liquid chromatography method presented
here is very fast, gives high resolutions, and enables collection of selected fractions containing nmoles of rare earth by
UV monitoring at 280 nm of the eluate. 相似文献
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Summary An isotope dilution method for the determination of rare earth impurities in uranium has been developed and Ce, Nd, Sm, Eu and Gd have been determined in uranium oxide samples. The method involves isotopic dilution with enriched isotopes of the rare earths being measured, followed by the separation of rare earths from uranium. A mass spectrometer with thermionic source was used to determine the relative isotopic abundances in each of these rare earths. All these five elements were analysed selectively by preferential evaporation technique. Trace concentrations down to parts per billion range can be measured with good sensitivity and accuracy.
Bestimmung von Verunreinigungen an Seltenen Erden in hochreinem Uran durch Isotopenverdünnungsanalyse
Zusammenfassung Eine Isotopenverdünnungsmethode wurde ausgearbeitet zur Bestimmung von Ce, Nd, Sm, Eu und Gd in Uranoxidproben. Das Verfahren umfaßt isotopische Verdünnung mit angereicherten Isotopen der zu bestimmenden Elemente und nachfolgende Abtrennung der Seltenen Erden von Uran. Die relativen Isotopenhäufigkeiten wurden mit Hilfe eines Massenspektrometers mit thermischer Ionenquelle bestimmt. Alle fünf Elemente wurden durch selektive Verdampfung analysiert. Spurenkonzentrationen bis herab zum ppb-Bereich konnten mit guter Empfindlichkeit und Genauigkeit erfaßt werden.相似文献
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A. I. Saleh J. R. W. Woittiez G. D. Wals H. A. Das 《Journal of Radioanalytical and Nuclear Chemistry》1990,144(3):165-172
The interferences by uranium fission on the determination by neutron activation analysis of Zr, Mo, Ru, La, Ce, Nd and Sm are investigated for the Argonaut-type Low Flux Reactor at ECN, Petten, The Netherlands. In addition, the spectral interference of the determination of Sm by239Np is considered. The experimental values for fission yields are found to be in good agreement with calculated values based on recent cross-section compilations. 相似文献
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The determination of individual light rare-earth metals in monazite sand is described, based on TLC with a mixture of di-isopropyl ether, diethyl ether, di(2-ethylhexyl)phosphate and nitric acid (8:8:0.4:0.07 v v ) as eluent. Linear densitometric calibration graphs are obtained for individual light rare-earths in the range 0.015-0.60 mug. The minimum detectable quantities of La. Ce, Pr, Nd and Sm are 9, 10, 20, 13 and 12 ng, respectively. The relative standard deviations for the determination of La, Ce, Pr, Nd and Sm in monazite sand were 1.8, 1.1, 5.9, 1.9 and 6.5%, respectively. Results were in good agreement with those obtained by spectrophotometry. 相似文献
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The simultaneous determination of lanthanide family elements is one of the greatest problems in analytical chemistry, due to the close similarity of their chemical properties. Spectrophotometric methods are generally of limited use, due to the various mutual spectral interferences involved. By using multivariate calibration methods (partial least-squares regression, PLSR), it was possible to obtain a model that adjusts itself perfectly to the values of the mixture concentrations used in the calibration. The model used absorption spectra in the 290-800 nm range for a set of 20 different mixtures of Ce, Pr, Nd and Sm, and made possible the determination of Ce, Pr and Nd concentrations of a commercial rare-earth product, with significantly greater precision than the conventional univariate calibration method. Determination of the Sm concentrations was not possible, since its concentration was below the concentrations used in the model definition. 相似文献
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本文提出了用电感耦合等离子体原子发射光谱(ICP—AES)法直接测定混合稀土铜合金中13个非稀土和稀土元素。选用了合适的分析线对及ICP光源的工作参数。探讨了观察高度、功率、酸度、载气和基体量的变化对被测元素谱线强度的影响。不用化学分离,可一次同时测定La、Ce、pr、Nd、Sm、Sn、Zn、Fe、Al、Ni、Pb,Mg和Mn。测定范围(%):La_2O_3:0.096~6.4;CeO_2:0.24~16;Pr_6O_(11):0.0384~2.56;Nd_2O_3:0.096~6.4;Sn:0.096~3.2;Mg、Mn、Fe,Sm_2O_3:0.024~1.6;Zn:0.396~6.7;Pb:0.092~6.4;Ni:0.096~3.2;Al:0.0384~1.28。相对标准偏差±3.0~9.1%;回收率85~116%满足冶炼上的要求,得到了满意的结果。 相似文献