用于~(18)N在~9Be、~(197)Au靶上破裂反应研究的探测器系统

描述了用于放射性核束 18N在 9Be、197Au靶上破裂反应研究的探测器系统构成、性能、特点及在线实验的初步结果。

28.7MeV/u的~(14,16,18)O+~(7,9)Be反应中的同位素分布研究

用同位旋相关的Boltzmann Langevin方程研究了在入射能量为2 8 7MeV/u下 ,不同弹核 14O ,16 O和 18O轰击不同靶核 7Be和 9Be的反应 ,计算了生成碎片的产生截面 ,发现用丰中子 (缺中子 )炮弹或丰中子 (缺中子 )靶进行反应 ,所得到的产物均有丰中子 (缺中子 )的碎片出现 .同位素分布宽度和峰位与入射体系密切相关 ,产生碎片的电荷数越接近入射弹核的电荷数 ,则同位素分布的宽度越大 ,峰位偏离β稳定线值越远 ,其同位旋效应越明显 .

60MeV/u~(18)O离子同天然铀反应钍的放化分离

用１－苯基－３－甲基－４－苯甲酰基吡唑啉酮－５（ＰＭＢＰ）作萃取剂，２３４Ｔｈ为示踪剂，对在ＨＮＯ３介质中用ＰＭＢＰ－苯萃取钍的条件实验进行了研究。在条件实验的基础上提出了一个从中能１８Ｏ离子照过的天然铀样品中简便、快速地分离钍的化学流程。钍样品的Ｙ射线谱显示该流程能去除绝大多数产物元素，特别是Ｕ、Ｃｅ和Ｉ的沾污。

~(18)O离子轰击厚靶的中子剂量学参数

用阈探测器活化法测量了每个核子动能（简称单核能）为５０ＭｅＶ１８Ｏ离子轰击厚靶（Ｂｅ、Ｃｕ、 Ａｕ）时出射中子的能量分布、注量率分布和中子角分布，得到了１８Ｏ离子的中子产额、前向中子发射率和中子剂量当量率分布的数据。并与国外报道的单核能在２０ＭｅＶ 以下的低能重离子轰击厚靶研究中得到的中子剂量学参数进行了比较和分析。

Single-electron capture in keV Ar15+...18++He collisions

Single-electron capture in 14 keV q(-1) Ar15+...18++He collisions is investigated both experimentally and theoretically. Partial cross sections and projectile scattering angle dependencies have been deduced from the target ion recoil momenta measured by the COLTRIMS technique. The comparison with close-coupling results obtained from a two-centre extension of the basis generator method yields good overall agreement, demonstrating the applicability of close-coupling calculations to collision systems involving highly charged ions in charge states up to 18+.

Production cross-section of Ra-230 in the reaction of 60 MeV/u O-18 ions with U-238

A thick natural uranium target was bombarded with a 60 MeV/u O-18 beam. The neutron-rich isotope Ra-230 as the target residue was produced through the multinucleon transfer reaction (U-238-4p-4n). The barium and radium fraction as BaCl2 precipitate were radiochemically separated first from the mixture of uranium and reaction products. Then, the radium fraction was separated from BaCl2 precipitate by using cation exchange technique. The gamma-ray spectra of the Ra fraction were measured using an HPGe detector. The production cross sections of Ra-230 were obtained by a combination of the radiochemical separation technique and off-line gamma-ray spectroscopy. The cross section of Ra-230 has been determined to be 66 +/- 20 mu b.

Production cross section of Th-236 in the interaction of U-238 with 60 MeV/u O-18 ions

The neutron-rich target-like isotope Th-236 has been produced in the U-238-2p multinucleon transfer reaction between a 60 MeV/u O-18 beam and natural U-238 targets. The activities of thorium were determined after radiochemical separation of Th from the mixture of uranium and reaction products. The Th-236 isotope was identified by the characteristic gamma-rays of 642.2, 687.6 and 229.6 keV. The production cross section of Th-236 was determined to be 250 +/- 50 mu b.

Production cross-section of Th-236 in the interaction of U-238 with 60MeV/u O-18 Ions

The neutron-rich target-like isotope Th-236 was produced in U-238-2p multinucleon transfer reaction between a 60MeV/u O-18 beam and nature U-238 targets. The thorium activities were radiochemically separated from the mixture of uranium and reaction products. The isotope Th-236 was identified by 642.2keV, 687.6keV and 229.6keV characteristic gamma-rays. The production cross section of Th-236 has been determined to be 250 +/- 50 mu b.

Experimental study of the two-proton correlated emission from the excited states of Ne-17,Ne-18 and S-28,S-29

A series of experiments have been performed by complete kinematics measurements to study two-proton (2p) correlated emission from the excited states of Ne-17,Ne-18 and S-28,S-29 via the Coulomb excitation by bombarding on Au-197 target. 2p and residua coincident events were picked Out under strict conditions. Visible p-p correlations were observed. It is shown that 2p can be emitted from the high-lying excited states. 2p halo may lead to 2p emission with large spectroscopy factor for the states close to or beyond the threshold.

Two-electron-one-photon M1 and E2 transitions between the states of the 2p(3) and 2s(2)2p odd configurations for B-like ions with 18 <= Z <= 92

Two-electron-one-photon (TEOP) M1 and E2 transition energies, line strengths and transition probabilities between the states of the 2p(3) and 2s(2)2p odd configurations for B-like ions with 18 <= Z <= 92 have been calculated using the GRASP2K package based on the multiconfiguration Dirac-Hartree-Fock (MCDHF) method. Employing active-space techniques to expand the configuration list, we have systematically considered the valence, core-valence and core-core electron correlation effects. Breit interaction and quantum electrodynamical (QED) effects were also included to correct atomic state wavefunctions and the corresponding energies. Influences of electron correlation, Breit interaction and QED effects on transition energies and line strengths of the TEOP M1 and E2 transitions were analysed in detail. The present results were also compared with other theoretical and experimental values.

The Synthesis and Characterization of a Novel (E,E)-Dioxime and its Mono- and Heterotrinuclear Complexes Containing an 18-Membered Dioxadithiadiazamacrocycle

The novel (E,E)-dioxime, 5,6:17,18-dibenzo-11,12-(4-nitrobenzo)-2,3-bis(hydroxyimino)-7,16-dithia-10,13-dioxa-1,4-diazacyclooctadecane) (H2L), has been synthesized from reaction of (E,E)-dichloroglyoxime (1) with 2,3:14,15-dibenzo 8,9-(4-nitrobenzo)-4,13-dithia-7,10-dioxa-1,16-diazahegzadecane (2). The mononuclear Co(III) complex (4) of this dioxime was prepared by oxidation of the cobalt (II) complex. The -capped Co(III) complex (5) was synthesized by using a precursor Co(III) complex and boron trifluoride dietherate. The heterotrinuclear complexes (6) and (7) were prepared by reaction of (5) with NiCl2·6H2O and CdCl2·H2O, respectively. In addition, the homotrinuclear Cu(II) complex (8), has also been prepared by the reaction of this dioxime with CuCl2·H2O. The structures of the dioxime and its complexes were identified by using elemental analysis, 1H- and 13C-NMR, IR, and mass spectral data.