首页> 外文期刊>Journal of Radioanalytical and Nuclear Chemistry: An International Journal Dealing with All Aspects and Applications of Nuclear Chemistry >Continuous separation of Sr, Y and some actinides by mixed solvent anion exchange and determination of ~(89,90)Sr, ~(238,239)Pu and ~(241)Am in soil and vegetation samples
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Continuous separation of Sr, Y and some actinides by mixed solvent anion exchange and determination of ~(89,90)Sr, ~(238,239)Pu and ~(241)Am in soil and vegetation samples

机译:通过混合溶剂阴离子交换法连续分离Sr,Y和某些act系元素,并测定土壤和植被样品中的〜(89,90)Sr,〜(238,239)Pu和〜(241)Am

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摘要

Methodology for the determination of ~(89,90)Sr, Am and Pu isotopes in complex samples is given. Methodology is based on simultaneous isolation of Sr, Y and actinides from samples by mixed solvent anion exchange chromatography, mutual separation of ~(89,90)Sr and ~(90)Y from actinides, mutual separation of Th, Pu and Am by extraction chromatography, quantitative determination of ~(89,90)Sr by Cherenkov counting and quantitative determination of Pu and Am isotopes in soil and vegetation samples by alpha spectrometry. It is shown that Y and Sr can be efficiently separated from alkaline, alkaline earth and transition elements as well as from lanthanides and actinides on the column filed by strong base anion exchanger in nitrate form and 0.25 M HNO_3 in mixture of ethanol and methanol as eluent. It is also shown that Pu, Am and Th strongly binds on the mentioned column, can be separated from number of elements and easily be eluted from column by water. After elution actinides were mutually separated on TRU column and electrodeposited on stainless steel disc. Examination of conditions of electrodeposition was shown that chloride-oxalate electrolyte with addition of DTPA in presence of sodium hydrogen sulphate in cell with cooling and rotating platinum anode enables deposition of actinides within 1 h by 0.8 A cm~(-2) current density. Obtained peaks FWHM for Pu, Am and Th isotopes are between 27 and 40 keV. Scanning electron microscopy picture and ED XRF analysis of electroplated discs showed that actinide deposition is followed by iron oxide formation on disc surface. The methodology was tested by determination of ~(89,90)Sr, Am and Pu isotopes in ERA proficiency testing samples (low level activity samples). Obtained results shows that ~(89,90)Sr, ~(241)Am and ~(238,239)Pu can be simultaneously separated on anion exchange column, ~(89,90)Sr can be determined by Cherenkov counting with a satisfactory accuracy and limit of determination within 1–3 days after separation. ~(241)Am and ~(238,239)Pu can easily be separated on TRU column and determined after electrodeposition with acceptable accuracy within 1 day.
机译:给出了测定复杂样品中〜(89,90)Sr,Am和Pu同位素的方法。方法学的基础是通过混合溶剂阴离子交换色谱法同时从样品中分离出Sr,Y和from系元素,从act系元素中互相分离〜(89,90)Sr和〜(90)Y,并通过萃取相互分离Th,Pu和Am色谱法,Cherenkov计数法定量测定〜(89,90)Sr以及通过α光谱法定量测定土壤和植被样品中的Pu和Am同位素。结果表明,在强碱阴离子交换剂以硝酸盐形式和0.25 M HNO_3在乙醇和甲醇的混合物中洗脱时,Y和Sr可以有效地与碱,碱土金属和过渡元素以及镧系元素和act系元素分离。还显示出Pu,Am和Th在上述色谱柱上牢固结合,可与多种元素分离,并容易被水洗脱。洗脱后,act系元素在TRU柱上相互分离,并电沉积在不锈钢圆盘上。电沉积条件的检查表明,在冷却和旋转铂阳极的情况下,在有硫酸氢钠存在的情况下,在电池中加入硫酸氢钠的氯化物草酸盐电解质和DTPA,能够在1 h内以0.8 A cm〜(-2)的电流密度沉积act系元素。 Pu,Am和Th同位素的峰FWHM在27至40 keV之间。电镀光盘的扫描电子显微镜照片和ED XRF分析表明,act化物沉积后在光盘表面形成氧化铁。通过确定ERA能力测试样品(低水平活性样品)中的〜(89,90)Sr,Am和Pu同位素来测试该方法。所得结果表明,〜(89,90)Sr,〜(241)Am和〜(238,239)Pu可以在阴离子交换柱上同时分离,〜(89,90)Sr可以通过Cherenkov计数法测定,具有令人满意的准确度和分离后1-3天内的测定极限。 〜(241)Am和〜(238,239)Pu可以很容易地在TRU色谱柱上分离,并在电沉积后1天内以可接受的精度进行测定。

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