HIRFL新的束流分配系统

随着CSR的建成和兰州重粒子加速系统(HIRFL)实现质子加速,HIRFL现有的束流传输系统已不能满足越来越多的物理实验对供束时间的要求,为此,对原有的HIRFL的束流输运系统进行了分时供束改造,新的束流分配系统可以在给CSR供束和不供束两种情况下,同时使用SFC和SSC的束流在多个实验终端进行物理实验,介绍了新设计的HIRFL束流分配系统的布局和束流光学计算结果.     

Optimization of separations of alkyl-substituted phenolate anions by capillary zone electrophoresis

Anions of alkylphenols have very similar electrophoretic mobilities in CZE owing to their very small differences in size and the narrow range of their pK_a values. By studying electrophoretic mobility as a function both of pH and of the amount of acetonitrile in the electrolyte solution, optimum separation conditions were determined. It was possible to separate a group of methyl-substituted phenols, including several positional isomers. Mixtures containing n-propyl and isopropyl phenols and 1°, 2°, and 3° butylphenols could be resolved.     

Direct Sensitization Up-conversion Mechanism in Er3+∶Yb3+ Co-doped Fluoride Materials

Up-conversion luminescence have been studied on Yb3+-Er3+ co-doped fluoride samples. Two infrared lasers with wavelength of 930 nm and 858 nm are carefully chosen as excitation sources. The experimental results suggest direct cooperation sensitization up-conversion rather than two-step sensitization up-conversion is responsible for the increased population of 2H11/2 (Er3+) and thus the increased green emission in the region 514～574 nm in Yb3+-Er3+ co-doped system.     

铈对纳米铁氧体粉末电磁学性质影响的研究

采用固相反应制备的Ce0 .2 5FeNiO3,FeNiO5,Fe3O4 ,Fe2 O34种纳米粉体 ,在 1～ 2 0 0 0MHz范围内进行了电磁学性质 (μ′,μ″ ,ε′,ε″)及吸波特性的比较研究。发现 4种纳米粉体的 μ′数据大小顺序为Ce0 .2 5FeNiO3>FeNiO5>Fe3O4 >Fe2 O3,μ″的变化幅度为Ce0 .2 5FeNiO3>Fe3O4 >FeNiO5>Fe2 O3。Ce0 .2 5FeNiO3的ε′和ε″的变化幅度大于其他几种纳米粉体。结果表明 ,加入稀土铈的铁氧体纳米粉体性能优于其他几种材料     

高纯氧化镨样品ICP摄谱分析时光谱干扰校正方法的研究

本文提出了Pr_6O_(11)样品ICP摄谱分析时干扰系数法校正光谱干扰的方法和相应的计算机软件系统。建立了Pr基体对14种稀土杂质元素24条灵敏分析线的干扰系数表(KCT),利用所提出的方法分析了Pr_6O_(11)合成样品,由91个实验点所得回收结果可知,回收率在90～110%之间的占93.4%。可见校正是相当有效和十分必要的。     

Zinc silicate-bonded diethyldithiocarbamate — a selective adsorbent for separating transition metal ions and preconcentration of palladium(II)

Summary A new chelating adsorbent, zinc silicate-bonded diethyldithiocarbamate (DTC) has been prepared for the separation and preconcentration of some transition metal ions. The distribution coefficients (Kd values) of 15 metal ions have been estimated in solution at various pH's and some quantitative separations have been achieved. The high selectivity for Pd(II) has been utilized for its preconcentration from dilute aqueous solutions; quantitative elution is effected with acidic 4% thiourea solution.     

Synthesis, structural characterization and properties of a 3D infinitely extended structural rare earth coordination compound of K3{[Sm(H2O)7]2Na[α-SiW11O39Sm(H2O)4]2}·14 H2O

A 3D infinitely extended structural rare earth coordination compound with a formula of K3{[Sm(H2O)7]2Na[α-SiW11O39Sm(H2O)4]2}·14H2O has been synthesized by reaction of Sm2O3, HClO4, NaOH with α-K8SiW11O39·nH2O, and characterized by IR,UV spectra, ICP, TG-DTA, cyclic voltammetry, variable-temperature magnetic susceptibility and X-ray single-crystal diffraction.X-ray single-crystal diffraction indicates that the title compound crystallizes in a triclinic lattice, Pī space group, with a=1.2462(3) nm, b=1.2652(3) nm,c=1.8420(4) nm,α=87.45(3)°,β=79.91(3)°,γ=82.57(3)°,Z=1, R1=0.0778,wR2=0.1610.Structural analysis reveals that Sm3+(1) coordination cation has incorporated into the vacant site of [α-SiW11O39]8- entity,forming the [α-SiW11O39Sm(H2O)4]5- subunit.The two adjacent [α-SiW11O39Sm(H2O)4]5- subunits are combined with each other through two Sm(1)-O-W bridges accompanying the formation of dimmer structural unit [α-SiW11O39Sm(H2O)4]210- of the title compound.The neighboring dimmer structural units [α-SiW11O39Sm(H2O)4]210- are linked to form the 1D chainlike structure by means of two Sm3+(2) and a Na+(1) coordination cations.The K+(1) cations connect the 1D packing chains constructing the 2D netlike structure, and adjacent netlike layers are also grafted by K+(2) cations to build the novel 3D infinitely extended structure.The result of TG-DTA curves manifests that the decomposition temperature of the title polyanionic framework is 554℃.The cyclic voltammetry measurements show that the title polyanion has the two-step redox processes in aqueous solution with pH=3.1.Variable temperature magnetic susceptibility indicates the title compound obeys the Cruie-Weiss Law in the higher temperature range from 110 to 300 K, while in the lower temperature range from 2 to 110 K the comparatively strong antiferromagnetism interactions can be observed.     

A Compact System of Capacitivity Coupled Contactless Conductivity Detection Based on the Square Wave Excitation Signal for Capillary Electrophoresis

This paper reported a compact system of capacitively coupled contactless conductivity detection （C4D） based on the square wave excitation voltage for capillary electrophoresis, and it exhibited excellent sensitivity at the optimal frequency of 198 kHz. The feasibility and sensitivity of this detector was demonstrated by simultaneous detection of thirteen ions including alkali, alkaline earth and heavy metal ions. And the detection limits （S/N 3） were in the range of 0.2-1μmol/L for Mn^2＋, K^＋, Na^＋, Mg^2＋, Ca^2＋, Li^＋, Ba^2＋, and 7-25 μmol/L for Ni^2＋, Cu^2＋, Cd^2＋, Pb^2＋, Co^2＋, Zn^2＋.     

Ir~( 49)M壳层共振自电离速率

研究了对电子碰撞激发速率共振自电离速率的影响，并且计算了类镍铱离子３ｄ到４ｌ共振激发速率，其作用对研究Ｘ射线激光设计、高温等离子体等诸多应用都有很重要的影响。