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1

Actinides produced by /sup 12/C + /sup 242/Pu and /sup 16/O + /sup 238/U reactions  

Energy Technology Data Exchange (ETDEWEB)

The cross sections for /sup 250/Fm, /sup 244-246/Cf, /sup 242-244/Cm, and /sup 242/Am/sup g-italic/ produced by the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions leading to the same compound nucleus of /sup 254/Fm have been measured by using radiochemical methods. The excitation functions show that the difference between the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions can be attributed mainly to the Coulomb barriers. Our results were compared with others reported previously for /sup 22/Ne+ /sup 232/Th, /sup 12/C+ /sup 238/U, /sup 12/C+ /sup 240,241/Pu, /sup 13/C+ /sup 241/Pu, /sup 16/O+ /sup 233/U, and /sup 16/O+ /sup 242/Pu reaction systems, and support a mechanism involving transfer of ..cap alpha..-particle clusters (C,Be,He) from projectile to target for the production of Cf and Cm isotopes.

1986-09-01

2

Actinides produced by /sup 12/C + /sup 242/Pu and /sup 16/O + /sup 238/U reactions  

International Nuclear Information System (INIS)

The cross sections for /sup 250/Fm, /sup 244-246/Cf, /sup 242-244/Cm, and /sup 242/Am/sup g/ produced by the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions leading to the same compound nucleus of /sup 254/Fm have been measured by using radiochemical methods. The excitation functions show that the difference between the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions can be attributed mainly to the Coulomb barriers. Our results were compared with others reported previously for /sup 22/Ne+ /sup 232/Th, /sup 12/C+ /sup 238/U, /sup 12/C+ /sup 240,241/Pu, /sup 13/C+ /sup 241/Pu, /sup 16/O+ /sup 233/U, and /sup 16/O+ /sup 242/Pu reaction systems, and support a mechanism involving transfer of #alpha#-particle clusters (C,Be,He) from projectile to target for the production of Cf and Cm isotopes.

3

Determination of americium and plutonium in autopsy tissue: methods and problems  

International Nuclear Information System (INIS)

The current methods used by the tissue analysis program at LASL for the determination of americium and plutonium in autopsy tissue are described. Problems affecting radiochemical yield are discussed. Included are problems associated with sample preparation, separation of plutonium from large amounts of bone ash, and reagent contamination. The average "2"4"2Pu tracer yield for 1800 Pu determinations is 78 +- 12%. The average "2"4"2Am tracer yield is 85 +- 7% for 40 determinations.

4

Determination of americium and plutonium in autopsy tissue: methods and problems  

Science.gov (United States)

The current methods used by the tissue analysis program at LASL for the determination of americium and plutonium in autopsy tissue are described. Problems affecting radiochemical yield are discussed. Included are problems associated with sample preparation, separation of plutonium from large amounts of bone ash, and reagent contamination. The average /sup 242/Pu tracer yield for 1800 Pu determinations is 78 +- 12%. The average /sup 242/Am tracer yield is 85 +- 7% for 40 determinations.

1979-01-01

5

Resonance ionization spectroscopy at {sup 240f,242f}Am fission isomers  

Energy Technology Data Exchange (ETDEWEB)

Optical Isotope shift measurements have been performed for the {sup 240f,242f}Am fission isomers to test the stability of nuclear deformation as function of the neutron number. The method is based on resonance ionization spectroscopy (RIS) in a buffer gas cell with fission detection of the ionization process. The {sup 240f,242f}Am fission isomers have been produced by {sup 242}Pu(p, 3n), {sup 242}Pu(d, 2n) reactions, respectively. Relative isotope shift ratios X{sub exp}{sup 242f}(500 nm)=IS{sup 242f,241}/IS{sup 243,241}=41.4(8) and X{sub exp}{sup 240f}(500 nm)=IS{sup 240f,241}/IS{sup 243,241}=39.2(8) were measured. From these ratios a small difference {delta}{beta}{sub 2}{sup 242f,240f}=0.0076(14) of the deformation parameter {beta}{sub 2} can be deduced assuming that the isotope shift between the reference isotopes {sup 241,243}Am is caused by a pure volume change. (orig.)

1997-10-01

6

Fragment angular momenta in low and medium energy fission of /sup 242/Pu  

Energy Technology Data Exchange (ETDEWEB)

Independent isomeric yield ratios of /sup 128/Sb were determined radiochemically in the thermal neutron induced fission of /sup 241/Pu and 34 MeV alpha particle induced fission of /sup 238/U, both involving the same compound nucleus (/sup 242/Pu). Fragment angular momenta estimated from the measured isomer ratios using the statistical model analysis showed significantly larger fragment angular momenta in the medium energy fissioning system compared to the low energy fissioning system. This has been attributed to the effect of higher excitation energy and angular momentum in the entrance channel leading to increased fragment temperature, moments of inertia and angular velocity. An attempt was made to calculate the fragment angular momentum in the medium energy fission using the Fermi gas model for the fissioning nucleus, taking into account the multichance fission, saddle shapes of the fissioning nuclei and the angular velocity components of the ...

1987-06-01

7

American National Standard: for nuclear criticality control of special actinide elements  

Energy Technology Data Exchange (ETDEWEB)

This standard is applicable to operations with the following: /sup 237/Np, /sup 238/Pu, /sup 240/Pu, /sup 241/Pu, /sup 242/Pu, /sup 241/Am, /sup 242m/Am, /sup 243/Am, /sup 243/Cm, /sup 244/Cm, /sup 245/Cm, /sup 247/Cm, /sup 249/Cf and /sup 251/Cf. Subcritical mass limits are presented for isolated fissionable units. The limits are not applicable to interacting units.

1981-01-01

8

Delayed neutron yields: Time dependent measurements and a predictive model  

Energy Technology Data Exchange (ETDEWEB)

The delayed neutrons from neutron-induced fission in /sup 232/U, /sup 237/Np, /sup 238/Pu, /sup 241/Am, /sup 242/Am/sup m/, /sup 245/Cm, and /sup 249/Cf were studied for the first time; those from /sup 232/Th, /sup 233/U, /sup 235/U, /sup 238/U, /sup 239/Pu, /sup 241/Pu, and /sup 242/Pu were measured again. The data were used to develop an expression for the prediction of the absolute delayed neutron yield, and the prediction of delayed neutron emission with time. This approach accurately predicts observed delayed neutron yields and decay characteristics. A fission product yield model was used in conjunction with delayed neutron emission probability to analytically predict delayed neutron characteristics. The results of this analysis are in excellent agreement with experimental values.

1981-03-01

9

Transmutation of minor actinides in high and representative neutron fluxes: the mini-INCA and MEGAPIE projects  

Energy Technology Data Exchange (ETDEWEB)

In the framework of nuclear waste transmutation studies, the Mini-INCA project has been initiated at CEA/DSM with objectives to determine optimal conditions for transmutation and incineration of minor actinides (MA) in high intensity neutron fluxes. Our experimental tools based on alpha- and gamma-spectroscopy of the samples and the development of micro fission chambers could gather either microscopic information on nuclear reactions (total or partial cross sections for neutron capture and/or fission reactions) or macroscopic information on transmutation and incineration potentials. Neutron capture cross sections of selected actinides ({sup 241}Am, {sup 242}Am, {sup 242}Pu, {sup 237}Np) have already been measured at ILL, showing some discrepancies when compared to evaluated data libraries but in overall good agreement with recent data. The studies and possibilities offer by the MEGAPIE project to assess neutronic performances of a 1 MW ...

2003-07-01

10

Transmutation of minor actinides in high and representative neutron fluxes: the mini-INCA and MEGAPIE projects  

International Nuclear Information System (INIS)

In the framework of nuclear waste transmutation studies, the Mini-INCA project has been initiated at CEA/DSM with objectives to determine optimal conditions for transmutation and incineration of minor actinides (MA) in high intensity neutron fluxes. Our experimental tools based on alpha- and gamma-spectroscopy of the samples and the development of micro fission chambers could gather either microscopic information on nuclear reactions (total or partial cross sections for neutron capture and/or fission reactions) or macroscopic information on transmutation and incineration potentials. Neutron capture cross sections of selected actinides ("2"4"1Am, "2"4"2Am, "2"4"2Pu, "2"3"7Np) have already been measured at ILL, showing some discrepancies when compared to evaluated data libraries but in overall good agreement with recent data. The studies and possibilities offer by the MEGAPIE project to assess neutronic performances of a 1 MW spallation target and the incineration of MA in a ...

2003-09-01

11

Review of integral data on higher transactinides  

International Nuclear Information System (INIS)

A review of the status of integral measurements is presented for "2"4"0Pu, "2"4"1Pu, "2"4"2Pu, "2"4"1Am and "2"4"3Am. This review includes integral measurements pertinent to thermal reactor systems, i.e., thermal cross sections and resonance integrals, as well as measurements for fast reactor systems. It appears that for these nuclides the data for thermal reactors are in good shape; however, more work is recommended in defining the branching ratio of the capture cross section of "2"4"1Am to the isomeric and ground states of "2"4"2Am. Also, benchmark irradiation data are needed for cross section data testing using depletion/production codes. For fast reactors, experiments are in progress, in the UK, in France, and also in the US, with partial results available at this time. Fast integral data obtained from these measurements will be very beneficial. The recommendation pertaining to "2"4"1Am and proper benchmarks for thermal reactor applications also applies to fast reactor ...

1979-05-01

12

DETERMINATION OF 237NP AND PU ISOTOPES IN LARGE SOIL SAMPLES BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY  

Energy Technology Data Exchange (ETDEWEB)

A new method for the determination of {sup 237}Np and Pu isotopes in large soil samples has been developed that provides enhanced uranium removal to facilitate assay by inductively coupled plasma mass spectrometry (ICP-MS). This method allows rapid preconcentration and separation of plutonium and neptunium in large soil samples for the measurement of {sup 237}Np and Pu isotopes by ICP-MS. {sup 238}U can interfere with {sup 239}Pu measurement by ICP-MS as {sup 238}UH{sup +} mass overlap and {sup 237}Np via {sup 238}U peak tailing. The method provides enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then transferring Pu to DGA resin for additional purification. The decontamination factor for removal of uranium from plutonium for this method is greater than 1 x 10{sup 6}. Alpha spectrometry can also be applied so that the shorter-lived {sup 238}Pu isotope can be measured successfully. {sup 239}Pu, {sup 242}Pu and {sup ...

2010-07-26

13

Alpha-spectrometric determination of uranium, plutonium, americium and curium isotope content in 'hot' particles and irradiated nuclear fuel  

International Nuclear Information System (INIS)

A method for express determination of "2"3"4"-"2"3"8U, "2"3"8"-"2"4"2Pu, "2"4"1"-"2"4"3Am and "2"4"2"-"2"4"4Cm content in fuel 'hot' particles and spent nuclear fuel is offered. The method is based on precision measurement of a sample #alpha# activity followed by estimate of relative contributions of individual nuclides, or groups of radionuclides, to total activity. Segregation in separate fractions of uranium, plutonium, americium and curium was made with the help of ion-exchange chromatography. Results are presented of "2"3"4"U, "2"3"8U, "2"3"8"Pu,"2"3"9"+"2"4"0Pu, "2"4"1Pu, "2"4"2Pu, "2"4"1"Am, "2"4"2"mAm, "2"4"3Am "2"4"2"Cm and "2"4"4Cm definition in 'hot' particles sampled in Chernobyl NPP surroundings, Opportunities to apply this method for identifying radionuclide content of spent nuclear fuel are discussed.

14

ZZ UKFY2, Fission Yields of Th, U, Np, Pu, Am, Cm, Cf Isotopes  

International Nuclear Information System (INIS)

Description of program or function: Format: ENDFB-6 format; Nuclides: Th-232, U-233, U-234, U-235, U-236, U-238, Np-237, Np-238, Pu-238, Pu-239, Pu-240, Pu-241, Pu-242, Am-241, Am-242, Am-243, Cm-243, Cm-244, Cm-245, and from the spontaneous fission of Cm-242, Cm-244, and Cf-252. Origin: New evaluation (Crouch 1, 2, 3, 4; UKFY1; JEF-1). A new evaluation of fission product yields from the thermal, fast, and 14 MeV neutron-induced fission of the following nuclides has been prepared in ENDFB-VI format: "2"3"2Th, "2"3"3U, "2"3"4U, "2"3"5U, "2"3"6U, "2"3"8U, "2"3"7Np, "2"3"8Np, "2"3"8Pu, "2"3"9Pu, "2"4"0Pu, "2"4"1Pu, "2"4"2Pu, "2"4"1Am, "2"4"2"mAm, "2"4"3Am, "2"4"3Cm, "2"4"4Cm, "2"4"5Cm; and from the spontaneous fission of "2"4"2Cm, "2"4"4Cm, and "2"5"2Cf

15

Spatial distributions of {sup 137}Cs and {sup 239+240}Pu in surface seawater within the Exclusive Economic Zone of East Coast Peninsular Malaysia  

Energy Technology Data Exchange (ETDEWEB)

The studies of {sup 137}Cs and {sup 239+240}Pu distributions in surface seawater at South China Sea within the Exclusive Economic Zone (EEZ) of Peninsular Malaysia were carried out in June 2008. The analysis results will serve as additional information to the expanded baseline data for Malaysia's marine environment. Thirty locations from extended study area were identified in the EEZ from which large volumes of surface seawater samples were collected. Different co-precipitation techniques were employed to concentrate cesium and plutonium separately. A known amount of {sup 134}Cs and {sup 242}Pu tracers were used as yield determinant. The precipitate slurry was collected and oven dried at 60 {sup o}C for 1-2 days. Cesium precipitate was fine-ground and counted using gamma-ray spectrometry system at 661.62 keV, while plutonium was separated from other radionuclides using anion exchange, electrodeposited and counted using alpha ...

2010-09-15

16

Rapid determination of "2"3"7Np and Pu isotopes in water by inductively-coupled plasma mass spectrometry and alpha spectrometry  

International Nuclear Information System (INIS)

A new method that allows rapid preconcentration and separation of plutonium and neptunium in water samples was developed for the measurement of "2"3"7Np and Pu isotopes by inductively-coupled plasma mass spectrometry (ICP-MS) and alpha spectrometry. "2"3"8U can interfere with "2"3"9Pu measurement by ICP-MS as "2"3"8UH"+ mass overlap and "2"3"7Np via peak tailing. The method provide enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then moving Pu to DGA resin for additional removal of uranium. The decontamination factor for uranium from Pu is almost 100,000 and the decontamination factor for U from Np is greater than 10,000. This method uses stacked extraction chromatography cartridges and vacuum box technology to facilitate rapid separations. Preconcentration is performed using a streamlined calcium phosphate precipitation method. Purified solutions are split between ICP-MS and alpha spectrometry so that long and short-lived Pu isotopes can be measured ...

2011-01-01

17

RAPID DETERMINATION OF 237 NP AND PU ISOTOPES IN WATER BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY AND ALPHA SPECTROMETRY  

Energy Technology Data Exchange (ETDEWEB)

A new method that allows rapid preconcentration and separation of plutonium and neptunium in water samples was developed for the measurement of {sup 237}Np and Pu isotopes by inductively-coupled plasma mass spectrometry (ICP-MS) and alpha spectrometry; a hybrid approach. {sup 238}U can interfere with {sup 239}Pu measurement by ICP-MS as {sup 238}UH{sup +} mass overlap and {sup 237}Np via peak tailing. The method provide enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then moving Pu to DGA resin for additional removal of uranium. The decontamination factor for uranium from Pu is almost 100,000 and the decontamination factor for U from Np is greater than 10,000. This method uses stacked extraction chromatography cartridges and vacuum box technology to facilitate rapid separations. Preconcentration is performed using a streamlined calcium phosphate precipitation method. Purified solutions are split between ICP-MS and alpha spectrometry so that long and ...

2010-06-23

18

PRELIMINARY CROSS SECTION AND NU-BAR COVARIANCES FOR WPEC SUBGROUP 26  

Energy Technology Data Exchange (ETDEWEB)

We report preliminary cross section covariances developed for the WPEC Subgroup 26 for 45 out of 52 requested materials. The covariances were produced in 15- and 187-group representations as follows: (1) 36 isotopes ({sup 16}O, {sup 19}F, {sup 23}Na, {sup 27}Al, {sup 28}Si, {sup 52}Cr, {sup 56,56}Fe, {sup 58}Ni, {sup 90,91,92,94}Zr, {sup 166,167,168,170}Er, {sup 206,207,208}Pb, {sup 209}Bi, {sup 233,234,236}U, {sup 237}Np, {sup 238,240,241,242}Pu, {sup 241,242m,243}Am, {sup 242,243,244,245}Cm) were evaluated using the BNL-LANL methodology. For the thermal region and the resolved and unresolved resonance regions, the methodology has been based on the Atlas-Kalman approach, in the fast neutron region the Empire-Kalman method has been used; (2) 6 isotopes ({sup 155,156,157,158,160}Gd and {sup 232}Th) were taken from ENDF/B-VII.0; and (3) 3 isotopes ({sup 1}H, {sup 238}U and {sup 239}Pu) were taken from JENDL-3.3. For 6 light nuclei ({sup 4}He, ...

2007-01-31

19

Highly enriched isotope samples of uranium and transuranium elements for scientific investigation  

International Nuclear Information System (INIS)

The paper describes the production of highly enriched isotopes of uranium, plutonium, americium and curium by electromagnetic separation for scientific and applied researches in physics, chemistry, geology, medicine, biology and other fields. Using the equipment described, the isotopes are produced in quantities sufficient to set up nuclear physical experiments, to produce nuclear reference materials and standard sources for calibration of radiometrical and mass spectrometrical equipment, in radionuclide metrology, etc. For the following isotopes the indicated degrees of isotopic enrichment were achieved: "2"3"3U-99.97%; "2"3"5U-99.97%; "2"3"6U-98.0%; "2"3"8U-99.997%; "2"3"8Pu-99.6%; "2"3"9Pu-99.9977%; "2"4"0Pu-99.9-100%; "2"4"1Pu-96.998%; "2"4"2Pu-97.8-99.96%; "2"4"4Pu-96.7%; "2"4"1Am-99.6%; "2"4"2"mAm-73.6%; "2"4"3Am-99.2-99.94%; "2"4"3Cm-99.99%; "2"4"5Cm-99.998%; "2"4"6Cm-99.8%; "2"4"7Cm-90%, "2"4"8Cm-97%. Methods for preparing layers of highly enriched isotopes on various ...

20

Calculated doses from inhaled transuranium radionuclides and potential risk equivalence to whole-body radiation  

International Nuclear Information System (INIS)

The distribution of radiation dose commitments within the body that can result from the lung deposition of a number of transuranic radionuclides ("2"3"7Pu, "2"3"8Pu, "2"3"9Pu, "2"4"0Pu, "2"4"1Pu, "2"4"2Pu, "2"4"3Pu, "2"4"4Pu, "2"4"1Am, "2"4"2Am, "2"4"3Am, "2"4"4Am, "2"4"2Cm, "2"4"3Cm, "2"4"4Cm, and "2"4"6Cm) was calculated. The variables that influence these organ dose commitments include the mobility of the particle or its dissolution products within the body, the radiation characteristics of the inhaled radionuclides and their progeny, and the size of the particles inhaled. In the calculation of organ dose commitments for whole-body, lungs, liver, bone tissues, kidneys, and gastrointestinal tract from the inhalation of transuranium radionuclides, physical characteristics of importance are the dimensions of the particle, its aerodynamic properties, and its density. For particles within the respirable size range, a useful description is provided by the activity median aerodynamic ...

1975-11-17

 
 
 
 
21

Application of a gamma spectroscopy system to the measurement of neutron cross sections necessary to the development of nuclear energy; Mise au point d'un systeme de spectroscopie pour mesurer des sections efficaces neutroniques applicables a un possible developpement du nucleaire comme source d'energie  

Energy Technology Data Exchange (ETDEWEB)

This work concerns the development of nuclear energy and nuclear waste management in particular. Two parts of this study can be distinguished. In the first part (theoretical), a thorium-plutonium fuel based on MOX and dedicated for PWR was investigated in order to transmute plutonium in a potentially low waste fuel cycle. It was shown that this type of fuel is not regenerative but could be used for a transition to the industrial thorium fuel cycle without building new reactors. Thanks to moderated neutron spectra and high loaded actinide mass in the core, U-233 is quickly created ({approx}300 kg/y) for a loss of about {approx}1200 kg of fissile plutonium. In the second part (experimental), we have developed and built a new reaction chamber to measure neutron cross sections of actinides by alpha-gamma spectroscopy. This experimental device (in principle transportable) was commissioned in the high flux reactor of ILL Grenoble. Neutron flux was measured by gamma spectroscopy of irradiated ...

2002-09-01

22

ZZ MCB-JEF2.2, MCB Continuous-Energy Neutron Cross Section Libraries for Temperatures from 300 to 1800 K  

International Nuclear Information System (INIS)

1 - Description of program or function: MCB-JEF2.2 is a continuous-energy cross section libraries in ACE Format suitable for the MCB-1C and MCNP codes. Libraries for various materials were generated at six different Temperatures, and cover the energy range up to 20 MeV. Format: ACE. Number of groups: Continuous energy. Nuclides: H-1, H-2, H-3, He-3, He-4, Li-6, Li-7, Be-9, B-10, B-11, C-nat., N-14, N-15, O-16, O-17, Na-23, F-19, Mg-nat., Al-27, Si-nat., P-31, S-32, S-33, S-34, S-36, Cl-nat, K-nat, Ca-nat., Ti-nat, V-nat, Cr-50, Cr-52, Cr-53, Cr-54, Mn-55, Fe-54, Fe-56, Fe-57, Fe-58, Co-59, Ni-58, Ni-59, Ni-60, Ni-61, Ni-62, Ni-64, Cu-nat, Ga-nat, Ge-72, Ge-73, Ge-74, Ge-76, As-75, Se-74, Se-76, Se-77, Se-78, Se-80, Se-82, Br-79, Br-81, Kr-78, Kr-80, Kr-82, Kr-83, Kr-84, Kr-85, Kr-86, Rb-85, Rb-86, Rb-87, Sr-84, Sr-86, Sr-87, Sr-88, Sr-89, Sr-90, Y-89, Y-90, Y-91, Zr-nat, Zr-90, Zr-91, Zr-92, Zr-93, Zr-94, Zr-95, Zr-96, Nb-93, Nb-94, Nb-95, Mo-nat, Mo-92, Mo-94, Mo-95, Mo-96, Mo-97, ...