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Evaluated spectroscopic data and level schemes from radioactive decay and nuclear reaction studies are presented for {sup 22}C, {sup 22}N, {sup 22}O, {sup 22}F, {sup 22}Ne, {sup 22}Na, {sup 22}Mg, {sup 22}Al, and {sup 22}Si. This evaluation for A = 22 supersedes the earlier one by R. B. Firestone (2005Fi16)
Experimental nuclear structure data from various reactions and decays have been evaluated for all known nuclides of mass 39 (Mg, Al, Si, P, S, Cl, Ar, K, Ca, Sc, Ti). Detailed evaluated nuclear structure information is presented for each reaction and decay and the best values combining all available data are recommended for level energies, half-lives, γ-ray energies and intensities, decay properties (energies, intensities and placement of radiations), and other spectroscopic data. The {sup 39}K, {sup 39}Ca and {sup 39}Ar are the most extensively studied nuclides; no excited states are known in {sup 39}Mg and {sup 39}Ti. This work supersedes the earlier full evaluation of A=39 by B. Singh and J. Cameron (2006Si02).
Experimental nuclear structure data from various reactions and decays are compiled and evaluated for all known nuclides with mass number A=138 (Sn,Sb,Te,I,Xe,Cs,Ba,La,Ce,Pr,Nd,Pm,Sm,Eu,Gd,Tb). Detailed evaluated nuclear structure information is presented for each reaction and decay and the best values combining all available data are recommended for level energies, half-lives, γ-ray energies and intensities, decay properties (energies, intensities and placement of radiations), and other spectroscopic properties. This work supersedes the previous full evaluation of A=138 by A.A. Sonzogni (2003So13).
The Chlorine Worth Study (CWS) was a critical experiment to address an urgent need for thermal chlorine nuclear data validation in plutonium systems. This urgent need is tied directly to plutonium recycle and recovery operations in the plutonium facility at Los Alamos National Laboratory, where exceptionally conservative criticality safety limits are used because no credit is taken for the neutron capture by chlorine. The experiment used weapons-grade plutonium metal plates clad in stainless steel, known as the PANN (plutonium aluminum no nickel) ZPPR (zero power physics reactor) plates. The plutonium was reflected and moderated by high-density polyethylene and included combinations of polyvinyl chloride (PVC) and chlorinated polyvinyl chloride (CPVC) as absorbers. The experiment and benchmark included three configurations mimicking 30 g 239 Pu/L plutonium, 300 g 239 Pu/L plutonium, and 600 g 239 Pu/L plutonium in an aqueous chloride solution. Uncertainties in the benchmark included five broad categories: (1) criticality measurement, (2) mass and density, (3) dimensions, (4) material compositions, and (5) positioning. The largest contribution to the overall uncertainties for all three cases came from the material compositions, in particular the PVC and CPVC absorber compositions. A detailed model was created to be a near match (that is within expectations of transport code users) and a simplified model was created to minimize offset dimensions and expedite modeling for code validation. Sample calculations were completed in MCNP6.3 with ENDF/B-VIII.0 and ENDF/B-VII.1 nuclear data. For the detailed and simplified models, the average difference between the computed and experimental k eff was 951 pcm. CWS will serve as the key validation experiment for nuclear criticality safety in support of aqueous chloride operations. The sensitivity to the chlorine capture cross section is orders of magnitude greater than other existing benchmarks. The current limits, as defined by nuclear criticality safety, are 520 g Pu per batch, i.e. the minimum critical mass of the Pu solution infinitely reflected by water [Criticality Handbook: Volume II, (1969)]. This extremely conservative critical mass limit does not credit any neutron capture by chlorine (in particular neutron capture by 35 Cl) and greatly impedes the throughput required for current and future operations.
Compilation of information about the structure of A = 3 systems. This review mainly summarizes the work presented in (2010Pu04) and has updates of mass, lifetime and nuclear moment data as noted in the text.
The experimental nuclear structure and decay data are evaluated for all the known nuclides of mass 50 (Cl, Ar, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni). Here, detailed evaluated nuclear structure information are presented in individual decay and reaction datasets and the best values are recommended in the Adopted dataset for level properties, γ and β radiations, and other spectroscopic information. No excited states are known in 50Cl and 50Ni, and limited information is available for 50 Ar, 50 K, 50 Fe and 50 Co. This work supersedes earlier evaluations of A=50 by 2011El01, 1995Bu09, 1990Bu18, 1984Al29, and 1976Au07.
Available nuclear structure information for the known A=256 nuclei (Cf, Es, Fm, Md, No, Lr, Rf and Db) is presented together with Adopted properties of levels and gamma rays. This evaluation supersedes data in the previous evaluations of A=256 nuclides by 1999Ak02, 1989Sc26, 1981Sc06 and 1976Sc02.
The experimental nuclear spectroscopic data for known nuclides of mass number 139 (Sn, Sb, Te, I, Xe, Cs, Ba, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy) have been evaluated and presented together with adopted properties for levels and gamma rays. This evaluation represents a revision of previous one (2001Bu16) by T.W. Burrows. Since then extensive new data have become available for many A=139 nuclides although, no excited state data are yet available for {sup 139}Sn, {sup 139}Sb, {sup 139}Tb, and {sup 139}Dy. The decay schemes of {sup 139}Sn, {sup 139}Sb, {sup 139}I, {sup 139}Tb and {sup 139}Dy nuclei are not known, and those for {sup 139}Gd and {sup 139}Eu are poorly known. Particle-transfer data are available for {sup 139}Ba, {sup 139}La, {sup 139}Ce and {sup 139}Pr. Limited high-spin data are available for {sup 139}Te, {sup 139}I, {sup 139}Cs, {sup 139}Ba, {sup 139}La and {sup 139}Ce, while such data are extensive for {sup 139}Pr, {sup 139}Nd, {sup 139}Pm, {sup 139}Sm, {sup 139}Eu and {sup 139}Gd. Recent {sup 139}Pm high-spin data from two independent studies using the same reaction and similar beam energy are in conflict and could be improved using state-of-the-art large gamma-detector arrays in contrast to the smaller arrays currently used. Cases for which no new experimental information are available since the last update have undergone checking resulting in some changes in the current work, but for the most part these are taken from the previous evaluations. Thus, the present work has greatly benefited from all prior NDS evaluations (2001Bu16, 1989Bu12, 1981Pe04, 1974Gr46), but at the same time data presented herein supersede those in the earlier evaluations.
Available information pertaining to the nuclear structure of all nuclei with mass numbers A=247 is presented. Various decay and reaction data are evaluated and compared. Adopted data, levels, spin, parity and configuration assignments are given. When there are insufficient data, expected values from systematics of nuclear properties or/and theoretical calculations are quoted. Unexpected or discrepant experimental results are also noted. A summary and compilation of the discovery of various isotopes in this mass region is given in 2013Fr02 ({sup 247}Pu, {sup 247}Am, {sup 247}Cm, {sup 243}Bk, {sup 247}Cf), 2011Me01 ({sup 247}Es), and 2013Th02 ({sup 247}Fm, {sup 247}Md)
The evaluated spectroscopic data are presented for known nuclides of mass 61 (Sc,Ti,V,Cr,Mn,Fe,Co,Ni, Cu,Zn,Ga,Ge). Excited-state data are nonexistent for {sup 61}Sc, {sup 61}Ti, {sup 61}V, and {sup 61}Ge. Significant amounts of new data have been added since the previous NDS evaluation of A=61 nuclides (1999Bh04). {sup 61}Sc nuclide is now experimentally known, but without any knowledge of its half-life. The ground state half-lives of {sup 61}Ti and {sup 61}V are now determined. Excited-state data have become available for {sup 61}Cr, {sup 61}Mn and {sup 61}Ga, while for {sup 61}Ge, five excited states were erroneously assigned in the previous evaluation, these have been omitted here. Improved and extensive high-spin excitations are available for {sup 61}Fe, {sup 61}Cu and {sup 61}Zn, including several new superdeformed structures in {sup 61}Cu and {sup 61}Zn. Thermal neutron capture γ-ray data are available in detail from 2004Ra23. The radioactive decay schemes of {sup 61}Sc and {sup 61}Ti are not known, while those for {sup 61}V, {sup 61}Fe and {sup 61}Ge are poorly known. This work benefited from the earlier full evaluations of A=61 published by 1999Bh04, 1983Ek01 and 1975Au05 and the one published in an ‘update’ mode by 1992Zh31. The data and conclusions presented in the current work supersede those in all the previous evaluations.
The experimental data are evaluated for known nuclides of mass number A = 42 (Al, Si, P, S, Cl, Ar, K, Ca, Sc, Ti, V, Cr). Detailed evaluated level properties and related information are presented, including adopted values of level and γ–ray energies, decay data (energies, intensities and placement of radiations), and other spectroscopic data. This work supersedes earlier full evaluations of A = 42 published by B. Singh, J.A. Cameron – Nucl.Data Sheets 92, 1 (2001) and P.M. Endt – Nucl. Phys. A521, 1 (1990); Errata and Addenda Nucl. Phys. A529, 763 (1991); Errata Nucl. Phys. A564, 609 (1993) (also P.M. Endt – Nucl. Phys. A633, 1 (1998) update). No excited states are known in {sup 42}Al, {sup 42}P, {sup 42}V and {sup 42}Cr, and structure information for {sup 42}Si and {sup 42}S is quite limited. There are no decay schemes available for the decay of {sup 42}Al, {sup 42}Si, {sup 42}P, {sup 42}V and {sup 42}Cr, while the decay schemes of {sup 42}Cl and {sup 42}Ti are incomplete in view of scarcity of data, and large gap between their Q–values and the highest energy levels populated in corresponding daughter nuclei. Structures of {sup 42}Ca, {sup 42}K, {sup 42}Sc and {sup 42}Ar nuclides remain the most extensively studied via many different nuclear reactions and decays.
Nuclear spectroscopic information for known nuclides of mass number 182 (Yb,Lu,Hf,Ta,W,Re,Os,Ir,Pt,Au, Hg,Tl,Pb) with Z=70 to 82 and N=112 to 100 have been evaluated and presented together with adopted energies and Jπ of levels in these nuclei. No excited state data are yet available for {sup 182}Y and {sup 182}Lu, while only limited structure information is available for {sup 182}Pb and {sup 182}Tl. Rotational band structures are known for {sup 182}Hg and {sup 182}Au but spin–parity assignments remain largely tentative. The decays of {sup 182}Lu, {sup 182}Hg, {sup 182}Au and {sup 182}Tl are not well established. The {sup 182}Hf isotope is of geophysical and astrophysical interest. This evaluation supersedes previous full evaluations of A = 182 published by 2010Si13, 1988Fi05 and 1975Sc13, and a selected (mainly high–spin) update of A = 182 published by 1995Si04. Only the Adopted properties of levels and gamma rays are presented in NDS, consult the ENSDF database at (www.nndc.bnl.gov/ensdf/) for details of individual reaction and decay datasets.
Nuclear spectroscopic information for experimentally investigated nuclides of mass 141 (Te, I, Xe, Cs, Ba, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, and Ho) has been evaluated. A summary of information obtained in various reaction and decay experiments is presented, together with data tables and adopted level schemes.
Spectroscopic data for all nuclei with mass number A = 70 have been evaluated, and the corresponding level schemes from radioactive decay and reaction studies are presented. Since the previous evaluation, the half-life of {sup 70}Mn has been measured and excited states in {sup 70}Fe observed for the first time. Excited states in {sup 70}Ni have been more extensively studied while Coulomb excitation and collinear laser spectroscopy measurements in {sup 70}Cu have allowed for firm Jπ assignments. Despite new measurements, there remain some discrepancies in half-lives of low lying states in {sup 70}Zn. New measurements have extended the knowledge of high-spin band structures in {sup 70}Ge and {sup 70}As. This evaluation supersedes the prior A = 70 evaluation of 2004Tu09.
Spectroscopic data for all nuclei with mass number A=136 have been evaluated and the corresponding level schemes from radioactive decay and reaction studies are presented. No excited states are known in {sup 136}In, {sup 136}Eu, or {sup 136}Gd and {sup 136}Tb remains unidentified. Discrepancies between experiments on isomeric decays in {sup 136}Sb and {sup 136}La suggest the need for futher experimental investigation. The decay of {sup 136}Eu has only been observed in a mixed source. The energy of the 17.5 s isomer in {sup 136}Cs was determined since the last evaluation, however, the branching ratio remains unknown. This work supersedes the earlier full evaluation of A=136 by A.A. Sonzogni (2002So05), and benefited tremendously from all previous evaluations of A=136.
Evaluated spectroscopic data and level schemes from radioactive decay and nuclear reaction studies are presented for {sup 26}O, {sup 26}F, {sup 26}Ne, {sup 26}Na, {sup 26}Mg, {sup 26}Al, {sup 26}Si, {sup 26}P, and {sup 26}S. This evaluation for A = 26 supersedes the earlier one by P. M. Endt (1998En04) and updates for some nuclides in ENSDF. Highlights of this evaluation are the following: This evaluation includes search results for {sup 26}S nuclide and its proton–decay mode (2011Fo08). An isomeric state (2.2 ms) in {sup 26}F has been discovered by 2013Le03. The state is proposed at 643.4 keV 1 from γ–ray measurements. Internal-transition and beta-decay branches for the state are also determined. New excited levels in {sup 26}Ne have been identified from {sup 26}F β{sup −} decay (2.2 ms). For some {sup 26}Si resonance states conflicting spin-parity assignments exist in the literature. These are identified by footnotes. 2015Do07 ({sup 3}He,nγ) propose the first 0+ state above proton separation energy at an excitation energy of 5890 keV and suggested for additional independent measurements to confirm or refute the existence of 5946 keV 4. 2016Ch09 consider 5946 keV level as a distinct excited state in their reanalysis of the literature data with possible spin-parity assignment of 0+ or 4+ This evaluation also includes discovery of an isomeric state, at 164.1 keV 1, in {sup 26}P by 2014NiZZ.
Spectroscopic data and level schemes from radioactive decay and nuclear reaction studies are presented here for all nuclei with mass number A=239. In general, a relatively small amount of new data on this mass chain has been reported since the previous evaluation in 2003. However, special evaluations, such as ''Database of prompt gamma rays from slow neutron–capture from elemental analysis'' (2007ChZX), have provided additional precise data for levels in 29 U. Also, new Coulomb excitation measurements in 239 Pu have extended the knowledge of the 1/2[631] rotational band up to Jπ=(55/2+)Jπ=(55/2+), and that of the octupole vibrational band up to Jπ=(53/2-)Jπ=(53/2-). For historical knowledge it is worth mentioning the report on the “Discovery of isotopes of the transuranium elements with 93 <= Z <= 98'' (2013Fr02), where the information for elements Np, Pu, Am, and Cf with mass number A=239 is presented. The alpha hindrance factors (HF) presented in this evaluation were calculated using values of the radius parameter (r 0 ) interpolated from those for even–even adjacent nuclei given by 1998Ak04.
We present available information pertaining to the nuclear structure of all nuclei with mass numbers A=243. Various decay and reaction data are evaluated and compared. Adopted data, levels, spin, parity and configuration assignments are given. When there are insufficient data, expected values from systematics of nuclear properties or/and theoretical calculations are quoted. Unexpected or discrepant experimental results are also noted. A summary and compilation of the discovery of various isotopes in this mass region is given in 2013Fr02 ( 243 Np, 243 Pu, 243 Am, 243 Cm, 243 Bk, and 243 Cf), 2011Me01 ( 243 Es), and 2013Th02 ( 243 Fm).