2014
DOI: 10.1016/j.aca.2014.04.044
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Americium and plutonium separation by extraction chromatography for determination by accelerator mass spectrometry

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Cited by 32 publications
(21 citation statements)
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“…The second strategy relies on the complete removal of the 241 Am in the 241 Pu material and setting the "clock" to zero (time zero). The amount of produced 241 Am by beta decay of 241 Pu (half-life 14.325 (24) years, k = 2 [18]) can be calculated at a given time using the appropriate Bateman equation [10]. The concentration of 241 Pu in the purified solution is determined by reverse IDMS using a certified plutonium spike CRM.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The second strategy relies on the complete removal of the 241 Am in the 241 Pu material and setting the "clock" to zero (time zero). The amount of produced 241 Am by beta decay of 241 Pu (half-life 14.325 (24) years, k = 2 [18]) can be calculated at a given time using the appropriate Bateman equation [10]. The concentration of 241 Pu in the purified solution is determined by reverse IDMS using a certified plutonium spike CRM.…”
Section: Methodsmentioning
confidence: 99%
“…Prior to the isotope ratio measurements, two purification steps were carried out to remove the 241 Pu from the in-grown 241 Am in the blends by means of UTEVA-spec [23] and DGA extraction resins [24] (both of Triskem International, Bruz, France). The time of the Am elution (i.e.…”
Section: Americium Purificationmentioning
confidence: 99%
“…AMS was also used recently to determine the ultra‐trace amounts of 241 Am in sediment and soil samples (Kazi et al, ). A single‐step DGA resin (normal: N,N,N′,N′‐tetra‐n‐octyldiglycolamide) extraction chromatography column was used to separate Pu and 241 Am from the sediment samples.…”
Section: Different Mass Spectrometric Techniques Used For Am and Its mentioning
confidence: 99%
“…Also, the presence of high salt content would create a deposit that would lead to loss of the energy of some alpha particles leading to a low energy tailing of the characteristic alpha energy peaks in the spectrum. Another method for alpha source preparation is microcoprecipitation of actinides with rare-earth fluoride like NdF 3 , and filtration deposition on smooth surface membrane having 0.1-0.2 mm pore size [1,11,12]. However, the most common method used for alpha spectrometry is the electrodeposition of actinides onto a polished metal (stainless-steel, silver, copper, nickel or platinum) cathode planchette/disc [13].…”
Section: Introductionmentioning
confidence: 99%