高电荷态离子Ar~(q+)与不同金属靶作用产生的X射线

研究了高电荷态离子Arq+(q=16,17,18)入射金属Be,Al,Ni,Mo,Au靶表面产生的X射线谱.实验结果表明,Ar的Kα-X射线是离子在与固体表面相互作用过程中固体表面之下形成空心原子发射的.电子组态1s2的高电荷态Ar16+离子在金属表面中性化过程中,存在的多电子激发过程使Ar16+的K壳层电子激发产生空穴,级联退激发射Ar的Kα特征X射线.Ar17+离子在金属表面作用过程中产生的X射线谱形与靶材料没有明显的关联,入射离子的Kα-X射线产额与其最初的电子组态有关,靶原子的X射线产额与入射离子的动能有关.

高电荷态离子~(40)Ar~(q+)与Au表面作用产生的X射线谱

利用光谱技术研究了高电荷态离子40Arq+(q=16,17,18)离子入射金属Au表面产生的X射线谱.分析结果表明,Ar的Kα-X射线是离子在与固体表面相互作用过程中在固体表面之下形成的空心原子发射的.当电子组态为1s2的高电荷态Ar16+离子在金属表面中性化过程中,存在着多电子激发过程使Ar16+的K壳层电子激发产生空穴,进而级联退激发射Ar的Kα特征X射线.入射离子的Kα-X射线产额与其最初的电子组态有关,靶原子的X射线产额与入射离子的动能有关.

X-ray spectra induced by slow highly charged Arq+ ions in collision with Nb surface

The X-ray spectra of Nb surface induced by Arq+ (q = 16,17) ions with the energy range from 10 to 20 keV/q were studied by the optical spectrum technology. The experimental results indicate that the multi-electron excitation occurred as a highly charged Ar16+ ion was neutralized below the metal surface. The K shell electron of Ar16+ was excited and then de-excited cascadly to emit K X-ray. The intensity of the X-ray emitted from K shell of the hollow Ar atom decreased with the increase of projectile kinetic energy. The intensity of the X-ray emitted from L shell of the target atom Nb increased with the increase of projectile kinetic energy. The X-ray yield of Ar17+ is three magnitude orders larger than that of Ar16+.

X-ray emission produced by interaction of highly ionized Arq+ ions with metallic targets

This paper studies the X-ray spectra produced by the interaction of highly charged ions of Arq+ (q = 16, 17, 18) with metallic surface of Be, Al, Ni, Mo and Au respectively. The experimental results show that the K alpha X-ray emerges from under the surface of solid in the interaction of ions with targets. The multi-electron excitation occurred in the process neutralization of the Ar16+ in electronic configuration of 1s(2) in metallic surfaces, which produces vacancy in the K shell. Electron from high n state transition to K vacancy gives off X-ray. We find that there is no obvious relation between the shape of X-ray spectra and the different targets. The X-ray yield of incident ions are associated with initial electronic configuration. The X-ray yield of target is related to the kinetic energy of the incident ions.

长江中游防护林工程区不同植被类型水土流失研究

对长江中游防护林体系灌沟集水区内的栓皮栎林、板栗林、灌木丛和坡地农田等４种植被类型的水土流失进行了研究．结果表明，４种植被类型土壤的总孔隙度变化范围为 ４０．９６％～４８．２０％，渗透速度变化为 ７．４４～１０．５８ｍｍ·ｍｉｎ~(－１)；地表径流、土壤以及Ｋ，Ｎ，Ｐ的流失量均为坡地农田＞栓皮栎林＞灌木丛＞板栗林．

聚丙烯酰胺对砂土保水性的影响

试验结果表明 ,施用聚丙烯酰胺可以加速土壤水分入渗 ,减少渗出量 ,抑制土壤水分蒸发 ,从而增强土壤的持水能力 .6kg土壤施用 0 2～ 0 .5g聚丙烯酰胺 ,土壤水分入渗时间为对照的 2 1%～ 6 .1% ,土壤水分渗出量为对照的 3 2 %～48.5 % ;土壤水分含量比对照高 2 % ,并可以降低土壤容重 ,形成良好的疏松结构

辽西低山丘陵荒坡营造水保林工程整地措施试验研究

为提高辽西半干旱地区营造水土保持林的成活率与质量，进行了工程整地措施试验。认为，造林前一年采取工程整地措施．能拦截坡面径充、拦蓄泥土、积存枯草（枝）落叶。较荒坡土壤含水量提高，土层厚０～１５ｃｍ为４．２％～７．５％，１５～３０ｃｍ为４．６％～８．５％；土壤有机质含量增加０．０３％～１．３７％；全氮增加　０．０１６％～０．０３１％，全磷提高０．００６％～０．０１４％；阳离子代换量高５．３０～　８．２４ｍｇ／１００ｇ土。土壤机械组成较荒坡粗沙比例降低，粘粒比例增高，物理性沙粒比例减少，物理性粘粒比例升高。给树木生长提供了良好的生态环境条件。造林成活率提高１０％～２５％，树木径粗增加０．１０～０．２８ｃｍ，树高增加１５．３％～９２．１％，树木长势显著好于荒坡造林。

黄土丘陵沟壑区山坡道路防蚀措施初步研究

山坡道路连接农田、果园 ,对山区经济发展有重要作用。黄土高原山坡道路存在严重的水土流失 ,侵蚀方式主要有沟蚀、泻溜、崩塌、陷穴、悬沟侵蚀与滑坡等。山坡道路网应按照小流域综合治理规划合理布置 ,其主要防护措施 :①修筑梯田 ,防止坡面径流冲刷道路 ;②将路面整修成拱形以分散径流 ;③在道路内侧修蓄水窑窖 ,拦蓄径流 ;④路面及边坡栽植草灌 ,防止雨水冲刷

云计算安全技术研究与趋势

云计算是计算机技术和互联网发展融合的又一里程碑,它将引领IT和信息领域的技术变革。随着云计算的发展和升温,有关云计算的思考和讨论呈现了更深入化和更实用化两个方向的发展。本文首先概述了云计算的起因和形成背景,介绍了云计算的发展历程及其发展现状,分析了云计算给IT及云安全带来的影响,结合当前的现状讨论了云计算与云安全的发展方向和应用前景。

二维分子形状和定量手性程度的研究

以二进制编码描述苯环型化合物分子在二维空间的形状,所得到的编码能够区分二维平面上一对苯环型化合物对映体。由于对映体的二进制编码不同,基于化合物和其镜像的编码计算得到了海明距离,并以其表征1对对映体的定量手性程度。以28对周长为22的手性苯环型化合物对映体为实例,计算苯环型化合物的定量手性程度,其结果仅仅有2个数值,分别为海明距离4和6。具有不同形状的该类化合物很多,为了提高分辨率,分别计算了窗口宽度从1～16时的海明距离,并分别以其来代表定量手性程度。结果显示全部16个窗口的海明距离的加和具有最大的区分能力,共得到17种海明距离。如果将每一窗口的细节引入到计算中,并采用类似的方法计算,则实例中所有的28个苯环型化合物实现了完全的区分,所得到的定量手性程度的区分能力是令人满意的。本研究证明如果用适当的编码来描述二维空间中分子的边界,能够解决分子形状的定量表征。尽管本文的二进制编码衍生于平...

Simultaneous determination of dopamine and ascorbic acid at an in-site functionalized self-assembled monolayer on gold electrode

The in-site functionalization of 4-aminothiophenol (4-ATP) self-assembled monolayer on gold electrode at physiological pH yields a redox active monolayer of 4'-mercapto-N-phenylquinone diimine (MNPD). The functionalized electrode exhibits excellent electrocatalytic responses towards dopamine (DA) and ascorbic acid (AA), reducing the overpotentials by about 0.22 V and 0.34 V, respectively, with greatly enhanced current responses. Due to its different catalytic activities toward DA and AA, the modified electrode resolves the overlapping voltammetric responses of DA and AA into two well-defined voltammetric peaks by differential pulse voltammetry (DPV), which can be used for the simultaneous determination of these species in a mixture. The catalytic peak current obtained from DPV was linearly related to DA and AA concentration in the ranges of 5.0 x 10-6 - 1.25 x 10-4 M and 8.0 x 10-6 - 1.3 x 10-4 M with correlation coefficient of 0.999 and 0.998, respectively. The detective limits (3sigma) for DA and AA were found to be 1.2 x 10-6 M and 2.4 x 10-6 M, respectively.

Electrocatalytic reduction of oxygen at multi-walled carbon nanotubes and cobalt porphyrin modified glassy carbon electrode

The multi-walled carbon nanotubes (MWNTs) modified glassy carbon electrode exhibited electrocatalytic activity to the reduction of oxygen in 0.1 M HAc-NaAc (pH 3.8) buffer solution. Further modification with cobalt porphyrin film on the MWNTs by adsorption, the resulted modified electrode showed more efficient catalytic activity to O-2 reduction. The reduction peak potential of O-2 is shifted much more positively to 0.12 V (vs. Ag/AgCl), and the peak current is increased greatly. Cyclic voltammetry (CV), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM), were used to characterize the material and the modified film on electrode surface. Electrochemical experiments gave the total number of electron transfer for oxygen reduction as about 3, which indicated a co-exist process of 2 electrons and 4 electrons for reduction of oxygen at this modified electrode. Meanwhile, the catalytic activities of the multilayer film (MVVNTs/CoTMPyP)(n) prepared by layer-by-layer method were investigated, and the results showed that the peak current of O-2 reduction increased and the peak potential shifted to a positive direction with the increase of layer numbers.

聚电解质溶液浓度区域的划分

按照DeGennes[1] 提出的标度概念 ,柔性高分子溶液可以划分为稀溶液 ,亚浓溶液和浓溶液 3个区域 ,它们之间分别以接触浓度c 和交叠浓度c 为分界线 .钱人元等[2 ] 根据聚苯乙烯溶液激基荧光强度浓度依赖性的实验结果 ,提出稀溶液区还应细分为极稀溶液和稀溶液两个区域 ,它的分界浓度称为动态接触浓度cs.中性高分子溶液存在这一分界浓度 ,已经得到体积排除色谱[3 ] 、高分子溶液的物理凝胶化[4] 、以及动态光散射[5] 等研究结果的证实 .本文作者之一 (程 )从中性高分子在溶液中由于范德华分子间吸引力的存在容易自缔合而形成团族的概念出发 ,导出了溶液粘度与cs 之间的理论关系[6,7] .聚电解质由于在溶液中可以离解为聚离子和对离子的特性 ,关于它的溶液浓度区域的划分问题 ,已经引发了一些理论的[8～ 11] 和许多实验的研究 ,其中包括光散射[12～ 14 ] 、小角X射线散射[15] 、小角中子散射[16] 、准弹性中子散射[17] 、溶液电导[18] 和溶液粘度[19]等 .这些研究中的绝大多数 ,仍然将溶液划分为稀溶液 ,亚浓溶液和浓溶液 3个区域.