HIRFL-CSR实验环中束流损失机制及寿命研究

分析了在储存环中回旋的离子束与残余气体分子、内靶和冷却电子束相互作用时的损失机制及相应的束流寿命,针对兰州重离子加速器冷却储存环实验环内靶模式,计算了50—500MeV/u12C6+,36Ar18+,132Xe54+和238U92+等束流在各种损失机制影响下所对应的束流寿命和总的束流寿命。结果表明:影响束流寿命的主要因素是与内靶分子(原子)之间的电荷交换及与冷却电子束之间的辐射复合;对于重离子束132Xe54+和238U92+,与冷却电子束之间的辐射复合是影响其储存寿命的主要因素。

Size modification of Au nanoparticles induced by slow highly charged ions Ar-40(q+) irradiation

Size modification of Au nanoparticles (NPs), deposited on the Au-thick film surface and irradiated by slow highly charged ions (SHCI) 40Arq+ (3 6 q 6 12) with fixed low dose of 4.3 1011 ions/cm2 and various energy ranging from 74.64 to 290.64 keV at room temperature (293.15 K), was investigated by atomic force microscopy (AFM) and transmission electron microscopy (TEM). The effect of projectile kinetic energy on the modified size of NPs was explored by an appropriate choice of the fixed process parameters such as ion flux, irradiation temperature, incident angle, irradiation time, etc. The morphological changes of NPs were interpreted by models involving collisional mixing, Ostwald ripening (OR) and inverse Ostwald ripening (IOR) of spherical NPs on a substrate. A critical kinetic energy as well as a critical potential energy of the projectile in the Au NPs size modification process were observed.

激光离子源用于A>170重丰中子新核素的研究

本文概述了 A > 170 质量区重丰中子同位素研究的主要工作和意义；介绍了 A > 170 重丰中子同位素合成、分离和鉴别方法；详细论述了激光离子源的原理、设计及其同传统离子源相比所具有的优越性；在文章结尾，设计了一个物理实验，实验目的在于：1）寻找 ~(181)Yb新核素；2）揭示天体物理学中~(180m)Ta 的产生问题。我们对反应截面进行了分析，并对产额进行了估计，证明了此实验设计的合理性，进而说明了带激光离子源的同位素分离器适用于产生截面很低的新核素和衰变研究。本文重点讨论了激光离子源的各方面问题：介绍了激光多步共振电离原理和激光离子源原理；具体分析了热毛细管式激光离子源元素选择性的产生及其影响的因素；讨论了在设计、加工过程中的具体问题；描述了所使用的激光技术；通过在线实验验证了热毛细管式激光离子源的元素选择性和分离效率。

长白山北坡植物群落复杂性的海拔梯度变化(英文)

应用梯度格局法在长白山北坡海拔700m-2600m的坡面上每100 m海拔设置一样地,共计20块样地,通过对同一群落各样方间的相异性测定,对各海拔植物群落的复杂性进行了分析。结果表明,以主林层乔木种的二元数据计算的结果,除亚高山岳桦林外,其它各海拔群落的样方间均表现出较高的相异性,特别是低海拔的阔叶红松林平均相异系数达0.74,明显高于其它植被类型;暗针叶林各群落间差异不大,相对而言1400 m群落样方间的相异性略高于其它群落,表现出过渡性群落树种组成的复杂性;岳桦林树种组成简单,样[(\267\275\274\344\322\262\261\355\317\326\263\366\275\317\270\337\265\304\\317\340\313\306\320\324\241\243)-0.1(\322\324\271\340\304\276\326\326\265\304\266\376\324\252\312\375\276\335\\274\306\313\343\265\304\310\272)]落内的相异性,虽低海拔的阔叶红松林总体上高于其它群落,但差异趋势并不像乔木种那么明显。以各草本植物与所有植物种的二元数据计算的各海拔群落内样方间的相异性,表现出非常相近的趋势,群落内样方间草本植物及所有植物种均以阔叶红松林及高山冻原差异最大,暗针叶林基本稳定于比较相近的水平。图3表1参8。

Multiphoton ionization of pyrrole-water mixed clusters

Multiphoton ionization of the hydrogen,bonded pyrrole-water clusters (C4H5N)(n)(H2O)(m) is studied with a reflectron-time of flight mass spectrometer at 355 mn. With increasing partial concentration of pyrrole in a gas mixture source, a series of poly-pyrrole-water binary-mixed cluster ions can be observed, including unprotonated cluster ions [(C4H5N)(x)(H2O)(y)](+), protonated cluster ions [(C4H5N)(x)(H2O)(y)](+) and dehydrogenated cluster ions [(C4H4N)(C4H5N)(x)(H2O)(y)](+). Ab initio calculations of their structures, bond strengths, charge distributions and reaction energies are carried out. Stable structures of these clusters are obtained from the calculations. A probable formation mechanism of the cluster ions [(C4H5N)(x)(H2O)(y)](+), [(C4H5N)(x)(H2O)(y)]H+ and [(C4H4N)(C4H5N)(x) (H2O)(y)](+) is supposed to be the ionization of clusters followed by dissociation.

Multiphoton ionization and ab initio calculation studies of pyridine-water mixed clusters using time of flight mass spectrometer

Multiphoton ionization of binary mixed clusters (C5H5N)(x)-(H2O)(y) at 532, 355 and 266 nm laser wavelengths has been investigated using TOF mass spectrometer. The experiments showed that almost all the products were protonated ions, At 532 and 355 nm, the products were mainly protonated pyridine clusters (C5H5N)(n)-H+, while at 266 nm, mixed binary cluster ions (C5H5N)(m)- (H2O)(n)-H+ appeared. It was found that the abundance of the [(C5H5N)(3)-H2O-H](+) ions was abnormally high. The calculation indicated that the ion [(C5H5N)(3)-H2O-H](+) is Of a kind of magic number structures with C-3v symmetry. A stepwise reaction mechanism is suggested that photoionization is followed by dissociation. (C) 2001 Elsevier Science B.V. All rights reserved.

痕量砷流动注射在线还原氢化物发生原子吸收测定

方法采用流动注射停流技术使水及土壤浸出液中Ａｓ（Ⅴ）在线还原为Ａｓ（Ⅲ），不经手工还原，用氢化物发生原子吸收光谱法直接测定砷的含量。含４ｍｏｌ／ＬＨＣｌ的样品溶液与３０％碘化钾溶液在编结式反应器中混合，并在采样环中停流４０ｓ，达完全还原后注入到载流中与硼氢化钠反应，采样速度５５次／ｈ，检出限（３σ）０．１μｇ／Ｌ对自来水和土壤浸出液的加标回收结果满意。

Proton transfer reactions within the pyridazine-methanol cluster ion

The multiphoton ionization of the hydrogen-bonding cluster pyridazine-methanol (C4H4N2-CH3OH) was studied using a time-of-flight mass spectrometer at the wavelengths of 355 and 532 nm. At both wavelengths, a series of protonated C4H4N2-(CH3OH)(n)-H+ cluster ions were obtained. Relevant ab initio calculations were performed with HF and B3LYP methods. Equilibrium geometries of both neutral and ionic C4H4N2-CH3OH clusters, and dissociation channels and dissociation energies of ionic clusters, are presented. The results show that when C4H4N2-CH3OH is vertically ionized, C4H4N2H+ and CH3O are the dominant products via proton transfer reaction. A high energy barrier makes another channel corresponding to the production of C4H4N2H+ and CH2OH disfavored. (C) 2002 Elsevier Science B.V. All rights reserved.