Four quasi-particle level at 2256 keV in182Re

In-beam nuclear spectroscopic studies of¹⁸²Re, following the reaction¹⁸¹Ta(α, 3n)¹⁸²Re have been made using gamma-ray and internal conversion electron techniques.K-conversion coefficients for several transitions have been measured and the multi-polarities of the various transitions assigned. In particular, the spin and parity of the four-quasi-particle isomeric level at 2256 keV were determined to be 16⁻. Theg-factor of this level has been measured to beg = 0·32 ± 0·05. On the basis of theg-factor and the decay pattern of this level, a configuration {v9/2⁺ [624↑]v7/2⁻ [514↓]v7/2⁻ [503↑]π9/2⁻ [514↑]} _k ^x = 16⁻ has been assigned to this level. The nature of the retardation of the gamma transitions deexciting this level is discussed. It is argued that the measured retardation factors can be explained if the nucleus has a triaxial shape.     

Restoration of rotational symmetry in deformed relativistic mean-field theory

We report on a very recently developed three-dimensional angular momentum projected relativistic mean-field theory with point-coupling interaction (3DAMP+RMF-PC). Using this approach the same effective nucleon-nucleon interaction is adopted to describe both the single-particle and collective motions in nuclei. Collective states with good quantum angular momentum are built projecting out the intrinsic deformed mean-field states. Results for ²⁴Mg are shown as an illustrative application.     

制样方法对初始各向异性砂土三轴剪切力学特性 的影响研究 1)

基于砂土颗粒的毛细效应特性和冻融试验原理,提出一种砂土试样制备方法,能够在0°~90°范围内任意选取沉积方向,且适用于不同颗粒级配的试样。在中围压条件下进行三轴固结排水剪切试验,研究结果表明,毛细效应、冻融相结合的制样方法能够减缓压缩剪切试验的应力-应变关系增长速度,降低试样的抗剪峰值强度,对残余强度的影响相对较弱。在其他应力路径条件下,例如拉伸、减压压缩、等应力压缩等试验中,可以不考虑装样方法的影响。建议的制样方法能够合理应用到砂土初始各向异性的研究工作中。     

邯郸与太原两地粉土动力特性的试验研究

对邯郸5个工程场区和太原1个工程场区的粉土进行了循环荷载幅值为不规则变化的动模量试验。试验研究发现,粉土的动模量衰减的比砂土慢;其动模量衰减到最大动模量的85%时,开始表现出塑性特征,因此,在动模量衰减到最大动模量的85%之前降低循环动荷载的幅值,动模量仍能大部分回到初始值。粘粒含量的变化使粘粒在粉土中表现出不同的作用,当粘粒含量小于10%时,动强度随粘粒含量的增加而降低;当粘粒含量大于10%后,动强度随粘粒含量的增加而增加。     

嵌入薄膜传感器悬臂梁三向力测量技术研究

以薄膜传感器悬臂梁作为等效模型,通过传感器的应变效应对三向力测量技术进行了研究。为提高薄膜传感器的应变输出响应,对悬臂梁上布放薄膜传感器的位置加设弹性结构,研究了三向力测力模型输出电压与传感器所在位置应变的关系;分析了受力位置对测力模型输出响应的影响关系,结合实验验证了其工作原理、测力模型应变输出响应与可控尺寸参数的关系。研究表明:该测力模型可实现三向力测量,各个方向最大测量误差均在9%以内,悬臂梁宽度方向x和高度方向z的交叉干涉误差分别为2.84%和3.37%;当悬臂梁自由端受力位置发生变化时,测力模型输出响应只在梁长度方向y上发生变化。     

Chiral geometry in multiple chiral doublet bands

The chiral geometry of multiple chiral doublet bands with identical configuration is discussed for different triaxial deformation parameters γ in the particle rotor model with πh_(11)/2γh_(11/2)~(-1).The energy spectra,electromagnetic transition probabilities B(M1) and B(E2),angular momenta,and K-distributions are studied.It is demonstrated that the chirality still remains not only in the yrast and yrare bands,but also in the two higher excited bands whenγ deviates from 30°.The chiral geometry relies significantly on γ,and the chiral geometry of the two higher excited partner bands is not as good as that of the yrast and yrare doublet bands.     

像素重要性测量特征下的侧扫声呐目标检测

研究了在较低信噪比下,在保证检测概率的前提下尽量降低虚警概率的目标检测,提出了一种针对特定目标的两阶段筛选算法.第一阶段中,首先使用阈值分割出有效点,并定义了一种新的像素重要性测量特征用于初步筛选目标。即通过有效像素点之间的距离来赋以高斯分布的权值,当前像素重要性的值定义为剩余有效点的距离加权和,具有较高的像素重要性值的聚集性强的区域内像素点会被定位出来。第二阶段,使用卷积神经网络分类器排除虚假目标.在实验中,使用近期无人潜器获得的海底数据,召回率与虚警概率分别达到90.39%与2.39%,证明了其相比声呐目标检测主流算法有更好的检测能力。     

模耦合理论计算纳米粒子在聚合物熔体中的含时扩散系数与常规扩散常数 (cited: 2)

分析和计算了纳米粒子在聚合物熔体中的含时扩散系数与常规扩散常数. 采用广义朗之万方程描述扩散动力学,并通过模耦合理论计算摩擦记忆内核.为简单起见,只考虑了来自两体碰撞和溶剂密度涨落耦合作用两类微观因素对摩擦记忆内核的贡献. 采用聚合物参考作用点模型以及Percus-Yevick闭合条件计算了聚合物-纳米粒子复合溶液的平衡态结构信息函数;详尽分析了纳米粒子的尺寸与聚合物链的尺寸对扩散动力学的影响. 揭示了结构函数、摩擦记忆内核以及扩散系数等随着纳米粒子半径和聚合物链长的变化关系. 结果表明,对于小尺寸的纳米粒子或者短链的聚合物,短时间的非马尔可夫扩散 动力学特征比较显著,含时扩散系数需要更长的时间弛豫到常规扩散常数. 微观因素对扩散常数的贡献随着纳米粒子尺寸的增加而减小,却随着聚合物链长的增加而增大. 此外,模耦合理论得到的扩散常数与Stokes-Einstein关系的预测值进行比较,发现对于小尺寸的纳米粒子或者长链的聚合物,微观因素对扩散常数的的贡献占主导地位. 相反,当纳米粒子较大或者聚合物链长较短时,流体力学的贡献会发挥重要作用.     

Comparisons of disposable and conventional silver working electrode for the determination of iodide using high-performance anion-exchange chromatography with pulsed amperometric detection

The paper compared the performance of two kinds of silver working electrode in electrochemical detector-the disposable and conventional electrode for the determination of iodide using high-performance anion-exchange chromatography (HPAEC) hyphenated with pulsed amperometric detection (PAD). The comparisons were carried out on the time of equilibration, long and short-term reproducibility, limits of detection and linearity of calibration. Results showed that disposable working electrode manifested equal or better results than conventional working electrode and could be used for iodide analysis. Besides, the disposable electrode could work for consecutive 2660 min (about 44 h, 10 min needed for each run) with no degradation. Due to its "disposable" property, disposable working electrode could be discarded if the detection sensitivity decreased to 80% so the time for polishing and reconditioning was spared and good reproducible results could be obtained. At last, the disposable electrode was applied for the determination of iodide in soil and sea water samples with the spiked recovery ranging from 96-104% and the detection limit of 0.5 microg/L (10 microL injection, three times of the baseline noise).     

Cholesterol complexes with tri-n-butylphosphate, tri-n-octylamine and cyclohexanone in chlorinated hydrocarbon solvents

The hydrogen bonding interactions of moderately associated cholesterol with tri-n-butylphosphate, tri-n-octylamine and cyclohexanone in dilute solutions of tetrachloromethane, 1,2-dichloroethane and trichloromethane were studied by conventional IR spectroscopy. Information on the stoichiometry of the complexes formed was derived from least squares plots of the linearized expressions of Bjerrum's degree of system formation. The formation constants of the complexes were also determined in this way. The spectra recorded in the OH region from 3100 to 3700 cm-1 were resolved in to the bands of the cholesterol species and the complexes formed. The complexes responsible for the observed bands were recognized from the dependence of their intensity on cholesterol monomer and free base concentration and from their frequency locations. The presence of the complexes B...HO(R) and B...HO(R)...HO(R) with tri-n-butylphosphate and tri-n-octylamine was established in all of the solutions and also for the system cholesterol+cyclohexanone in 1,2-dichloroethane. On the other hand, for cholesterol bonding to cyclohexanone in tetrachloromethane, the model considering complexes with 3:1 and 1:1 stoichiometry seemed the most appropriate.