241Am (n,gamma) isomer ratio measurement

Conference · Wed Jan 05 00:00:00 EST 2011

OSTI ID:1045420

Bond, Evelyn M ^[1]; Vieira, David J ^[1]; Moody, Walter A ^[1]; Slemmons, Alice K ^[1]

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1. Los Alamos National Laboratory

The objective of this project is to improve the accuracy of the {sup 242}Cm/{sup 241}Am radiochemistry ratio. We have performed an activation experiment to measure the {sup 241}Am(n,{gamma}) cross section leading to either the ground state of {sup 242g}Am (t{sub 1/2} = 16 hr) which decays to {sup 242}Cm (t{sub 1/2} = 163 d) or the long-lived isomer {sup 242m}Am (t{sub 1/2} = 141 yr). This experiment will develop a new set of americium cross section evaluations that can be used with a measured {sup 242}Cm/{sup 241}Am radiochemical measurement for nuclear forensic purposes. This measurement is necessary to interpret the {sup 242}Cm/{sup 241}Am ratio because a good measurement of this neutron capture isomer ratio for {sup 241}Am does not exist. The targets were prepared in 2007 from {sup 241}Am purified from LANL stocks. Gold was added to the purified {sup 241}Am as an internal neutron fluence monitor. These targets were placed into a holder, packaged, and shipped to Forschungszentrum Karlsruhe, where they were irradiated at their Van de Graff facility in February 2008. One target was irradiated with {approx}25 keV quasimonoenergetic neutrons produced by the {sup 7}Li(p,n) reaction for 3 days and a second target was also irradiated for 3 days with {approx}500 keV neutrons. Because it will be necessary to separate the {sup 242}Cm from the {sup 241}Am in order to measure the amount of {sup 242}Cm by alpha spectrometry, research into methods for americium/curium separations were conducted concurrently. We found that anion exchange chromatography in methanol/nitric acid solutions produced good separations that could be completed in one day resulting in a sample with no residue. The samples were returned from Germany in July 2009 and were counted by gamma spectrometry. Chemical separations have commenced on the blank sample. Each sample will be spiked with {sup 244}Cm, dissolved and digested in nitric acid solutions. One third of each sample will be processed at a time. First, the gold will be removed by anion exchange chromatography. Then the {sup 242}Cm will be separated from the {sup 241}Am using the methanol/nitric acid anion exchange method. When a sufficient separation has been achieved, a deposit will be prepared and the {sup 242}Cm will be counted by alpha spectrometry. The purified {sup 241}Am fraction containing the long lived {sup 242m}Am will be allowed to decay into {sup 242}Cm for a period of {approx}6 months. After this time, the americium/curium separations will be repeated and the {sup 242}Cm that has grown in will be counted by alpha spectrometry. At the conclusion of the experiment, we will have cross section measurements for {sup 241}Am (n,{gamma}) {sup 242g}Am and {sup 241}Am (n,V) {sup 242m}Am at two energies.

• Research Organization: Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC52-06NA25396
• OSTI ID: 1045420
• Report Number(s): LA-UR-11-00067; LA-UR-11-67; TRN: US1203618
• Resource Relation: Conference: Nuclear Detonation Detection Forensics Program Review NA-22 ; January 11, 2011 ; Cocao Beach, Fl
• Country of Publication: United States
• Language: English

Related Subjects

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS
73 NUCLEAR PHYSICS AND RADIATION PHYSICS
ALPHA SPECTROSCOPY
AMERICIUM
ANIONS
CAPTURE
CHROMATOGRAPHY
CROSS SECTIONS
DETECTION
EXPLOSIONS
FORSCHUNGSZENTRUM KARLSRUHE
GAMMA SPECTROSCOPY
GROUND STATES
ISOMER RATIO
ISOMERS
NEUTRON FLUENCE
NEUTRON REACTIONS
NEUTRONS
NITRIC ACID
RADIOCHEMISTRY
TARGETS