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Featured researches published by P.R. Fields.


Physics Letters B | 1967

Nuclear properties of 242Cf, 243Cf, 244Cf and 245Cf☆

P.R. Fields; R.F. Barnes; R.K. Sjoblom; J. Milsted

Abstract Irradiation of 242 Cm and 244 Cm by 3 He ions produced two new isotopes of californium; 242 Cf emits a 7.35 ± 0.01 MeV α-particle group and has a half-life of 3.2 ± 0.5 min, 243 Cf emits 7.06 ± 0.01 and 7.17 ± 0.01 MeV α-particle groups and decays with a half-life of 12.5 ± 1.0 min. New values for the α-particle energies and half-lives were obtained for 244 Cf and 245 Cf.


Nuclear Physics | 1970

Nuclear decay properties of light einsteinium isotopes

I. Ahmad; R.K. Sjoblom; R.F. Barnes; E.P. Horwitz; P.R. Fields

Abstract The light einsteinium isotopes 248 Es, 249 Es, 250 Es and 251 Es were synthesized by irradiating a 249 Bk target with 3 He and 4 He ions. Because of the short half-life of 248 Es, it was necessary to characterize this isotope by using the recoil technique, whereas the other isotopes were chemically purified before their properties were determined. The half-lives of the above nucleides were found to be 28 ± 5 min, 1.7 ± 0.1 h, 8.3 ± 0.2 h and 33 ± 1 h, respectively. A new isomer of 250 Es was discovered and its half-life was determined to be 2.1 ± 0.2 h. The energies of the main α groups for 248 Es, 249 Es and 251 Es were observed to be 6.87 ± 0.01, 6.770 ± 0.005 and 6.488 ± 0.005 MeV, respectively. The α/K X-rays ratio for 249 Es was found to be 0.007 ± 0.001 and the value for 251 Es was 0.008±0.002. Several gamma rays associated with the electron-capture decay of the einsteinium isotopes were observed. On the basis of the present investigation the ground states of 249 Es and 251 Es have been assigned to the Nilsson states 7 2 + (633↑) and 3 2 − (521↑) , respectively.


Science | 1966

Copper Artifacts: Correlation with Source Types of Copper Ores

Alan M. Friedman; M. Conway; M. Kastner; J. Milsted; Donald N. Metta; P.R. Fields; E. Olsen

Six out of eight minor chemical elements, determined by spectroscopic and neutron-activation techniques, were found to be critical in computing a probability that a given copper artifact was derived from one of three types of copper ore: native metal, oxidized ore, reduced ore. Two elements, gold and tin, were apparently alloyed deliberately in many artifacts from both the Old World and the New World.


Nuclear Physics | 1970

Nuclear properties of 254Md, 255Md, 256Md, 257Md and 258Md

P.R. Fields; I. Ahmad; R.F. Barnes; R.K. Sjoblom; E.P. Horwitz

Abstract The isotopes 254–258Md were produced by irradiating an Es target with 4He ions and their nuclear properties were investigated. A chromatographic separation procedure was utilized to obtain pure Md samples. The half-lives of 255Md, 256Md, 257Md and 258Md were found to be 27 ± 2 min, 75 ± 4 min, 5.4 ± 0.5 h and 56 ± 7 d, respectively, and are in agreement with previously reported values. The α/(α+EC) ratios for 255Md, 256Md and 257Md were measured to be 7 ± 1 %, 8.5 ± 0.8 % and 10 ± 3 %, respectively. The main a groups of 255Md, 256Md, 257Md and 258Md were found to have energies of 7.322 ± 0.005, 7.202 ± 0.005, 7.064 ± 0.005 and 6.716 ± 0.005 MeV, respectively. The nucleide 254Md was observed for the first time and was found to decay by EC with a half-life of 10 ± 3 min. Successive chemical separations of Fm indicate the existence of another 254Md isomer having a half-life of 28 ± 8 min.


Journal of Inorganic and Nuclear Chemistry | 1968

Fission cross-sections for 243Pu, 250Bk, 247Cm, 245Cm, 254mEs and 254Es, and odd-odd systematics☆

H. Diamond; J.J. Hines; R.K. Sjoblom; R.F. Barnes; Donald N. Metta; J. Lerner; P.R. Fields

Abstract Fission cross-sections measured in back-to-back ion chambers in a graphite thermal column of a reactor are: 243 Pu, 196±16 barns; 250 Bk, 960±150 barns; 247 Cm, 108±5 barns; 245 Cm, 2040±80 barns; 254m Es, 1840±80 barns; 254 Es, 3060±180 barns. A more accurate beta decay half-life of 4·955±0·003 hours was found for 243 Pu. Of the 12 known thermal neutron fission cross-sections for odd-neutron and odd-proton target nuclei, only one cross-section is more than a factor of 2·3 from 1350 barns. A more striking uniformity is observed in the ratio of thermal neutron fission cross-section to target spin: eight of the ten known ratios are grouped at 600±320 barns per spin unit. The dependency of fission cross-section upon target spin is also shown by the three sets of isomers ( 254 Es, 242 Am, 244 Am) in which the higher fission cross-section of each pair is associated with the higher spin isomer. No simple correlation between fission cross-section and calculated compound nucleus level-density was found.


Journal of Inorganic and Nuclear Chemistry | 1961

Solvent extraction of actinides and lanthanides from molten salts

N.M. Isaac; P.R. Fields; Dieter M. Gruen

Abstract For the first time, quantitative measurements have been made of distribution coefficients of metal ions between a fused salt phase and an organic phase. The measurements were made at a temperature of 150°C using a LiNO 3 KNO 3 eutectic (m.p. 120°C) and tributyl phosphate (TBP) as the active extractant with a mixture of polyphenyls as the inert diluent. Distribution coefficients were determined for Co(II), Eu(III), Nd(III), Am(III), Cm(III), Np(V), Np(VI) and U(VI), and found to be higher by a factor of ∼10 2 –10 3 as compared with concentrated aqueous nitrate solutions. The number of TBP molecules associated with the complexes M(NO 3 ) p . (TBP) q in the organic phase were found to be the same [except for Co(II)] as those reported for aqueous nitrate system. The effect of Cl − addition to the nitrate melt was to lower the distribution coefficients. The separation factor 3·2 for Am(III)/Cm(III) suggests a possible application to the separation of these two elements.


Journal of Inorganic and Nuclear Chemistry | 1972

Electron capture decay of 240Am

I. Ahmad; R.F. Barnes; R.K. Sjoblom; P.R. Fields

Abstract The γ-ray and conversion electron spectra of mass-separated 240Am samples were measured with high-resolution Ge(Li) and Si(Li) spectrometers. The conversion coefficients of the 42·9, 99·0, 888·7 and 987·7 keV transitions were measured and their multipolarities were established as E2. A ce−-γ-ray coincidence experiment showed that the 888·7 and 987·7 keV transitions originate from a 1030·6 keV level. On the basis of the measured log ft value the ground state of 240Am has been given a spin-parity assignment of 3- with the configuration {n[631] 1 2 +; p[523] 5 2 −} . The 1030·6 keV level of 240Pu has been given a spin-parity assignment of 3+ with the two-quasi-particle configuration {n[631] 1 2 +; n[622] 5 2 +} . Several other low intensity γ-rays were observed. The half-life of 240Am was measured to be 50·8 ± 0·3 hr which is in agreement with previously reported values.


Nuclear Physics | 1967

Some new properties of 254Es and 255Es

P.R. Fields; H. Diamond; A.M. Friedman; J. Milsted; J. Lerner; R.F. Barnes; R.K. Sjoblom; Donald N. Metta; E.P. Horwitz

Abstract Alpha decay of the 39.3 h 254m Es isomer was observed and further studies showed that this decay populates a 2 − excited state in 250 Bk, but decay to the 2 − ground state is highly hindered. The partial alpha half-life of 254m Es is 1.52±0.1 y. A lower limit to the spontaneous fission half-life of 254 Es was set at 2.5 × 10 7 y. The total decay and partial spontaneous fission half-lives of 254 Fm were redetermined as 194.4±0.1 min and 228±1 d, respectively. The pile neutron cross sections of 253 Es to produce the two isomers of 254 Es were measured as σ c = 13 b ( 254 Es ), σ c = 338 b ( 254 m Es ) . The partial alpha half-life of 255 Es has been measured as 1.38±0.08 y and the partial spontaneous fission half-life as 2440±140 y. The rotational band structure observed in the alpha decay of 255 Es is consistent with a 7 2 + spin.


Journal of Inorganic and Nuclear Chemistry | 1958

The absorption spectrum of aqueous curium (III)

W.T. Carnall; P.R. Fields; D.C. Stewart; T.K. Keenan

The absorption spectrum of aqueous curium (III) has been studied in 0·04 N HClO4, using the isotope 244Cm. Three prominent absorption peaks have been discovered at 3754 A, 3812 A and 3965 A, in addition to absorption in the far ultra-violet. These same peaks are found in HCl, HNO3 and H2SO4 solutions. The general characteristics of the spectra in these three acids and some general observations on the radiation decomposition of aqueous curium solutions are reported.


Nuclear Physics | 1972

Electron capture decay of 238Am and electric monopole transitions in 238Pu

I. Ahmad; R.K. Sjoblom; R.F. Barnes; F. Wagner; P.R. Fields

Abstract Mass-separated samples of 238 Am (T 1 2 = 98 min ) have been used to investigate the EC decay scheme of 238 Am. The γ-ray and conversion electron spectra were measured with high-resolution Ge(Li) and Si(Li) spectrometers. Several electric monopole transitions were identified. The K/L ratios of the EO transitions are in agreement with the theoretical values of Church and Weneser. A γ-ray spectrum was measured in coincidence with the electron lines of the 44.1 keV transition in order to distinguish transitions going to the ground state from those terminating at the 2 + or 4 + member of the ground state band. From these data a decay scheme has been constructed. Assignments of levels already known from the β − decay of 2338 Np and α-decay of 242 Cm have been confirmed. Several other low-spin states have been postulated to account for the observed γ-rays and conversion electrons. From log ft value considerations the ground state of 238 Am has been given an assignment of { n [743] 7 2 − ; p [523] 5 2 − }1 + and the 962.8 keV level of 238 Pu has been assigned to { n [743] 7 2 − ; n [622] 5 2 + }1 − . The half-life of 238 Am has been measured to be 98±3 min. A 5.94 MeV α-group has been assigned to 238 Am decay. The α-branching has been measured to be (1.0±0.4)×10 −4 %.

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A.M. Friedman

Argonne National Laboratory

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H. Diamond

Argonne National Laboratory

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R.F. Barnes

Argonne National Laboratory

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M.H. Studier

Argonne National Laboratory

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R.K. Sjoblom

Argonne National Laboratory

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I. Ahmad

Argonne National Laboratory

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J. Milsted

Argonne National Laboratory

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J. Lerner

Argonne National Laboratory

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Donald N. Metta

Argonne National Laboratory

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