基于PVM的并行调试环境

并行软件开发环境的研究已日益成为并行计算和并行处理的重点。本文简介了可移植的消息传递环境ＰＶＭ，讨论了以此为目标的图形监视环境ＸＰＶＭ，阐明ＸＰＶＭ环境与实际需要的ＰＶＭ并行调试环境之间的差距，并在此基础上探讨了并行调试环境开发中的技术难点及其设计要求。     

The distribution of nutrient elements in cell wall and other fractions of the herbage of some grasses and legumes

The distribution of 10 nutrient elements was assessed in three fractions of herbage samples of perennial ryegrass, tall fescue, white clover and lucerne. The cell wall fraction, prepared by mechanical disintegration of undried material, contained the following proportions of the total herbage content of the major elements: N, 2.9–16.4%; P, 3.0–6.9%; S, 3.6–17.2%; Ca, 11.3–51.8%; Mg. 6.4–27.6% and K, 0.1–1.7%. Substantial though more variable proportions of the trace element cations, Fe, Mn, Zn and Cu were also present in the cell wall fraction. The extent to which the elements were soluble in water was assessed by analysis of the water-insoluble fraction prepared from freeze-dried samples of each herbage. The proportions of the total herbage content of the major elements soluble in water were: N, 30–57%; P, 80–92%; S, 35–71%; Ca, 48–69%; Mg. 65–83% and K, 90–96%. With the trace element cations the proportions soluble in water were more variable, though they were generally less than 70% of the total. The extent to which the various elements were soluble in 80% aqueous ethanol was assessed by analysis of the insoluble fraction prepared from freeze-dried materials. With each of the major elements, smaller proportions of the total herbage content were soluble in 80% ethanol than in water, which may reflect in part the lower solubility of proteins and pectin. With the trace element cations, the differences in solubility between 80% ethanol and water were generally small and inconsistent.     

微量Si在W—7Ni—3Fe重合金中的行为

研究了掺到原料Ｗ粉中微量Ｓｉ（４００ｐｐｍ）在Ｗ－７Ｎｉ－３Ｆｅ重合金中的分布及在液相烧结过程中的行为。结果表明，Ｓｉ主要以固溶形式分布在Ｗ晶粒中。Ｘ射线光电子能谱（ＸＰＳ）分析发现，在掺杂Ｓｉ的Ｗ－Ｗ及Ｗ－基体相界面富集ＳｉＯ２和Ｎａ２ＳｉＯ３在未掺杂试样的断口表面发现了较弱的ＷＯ２的ＸＰＳ谱，而在掺杂合金中未发现ＷＯ２。     

深海声速剖面对吊放声纳探测距离的影响研究

关于深海环境下声纳目标探测优化问题,针对传统吊放声纳的下放深度比较粗略,一般是在声道轴处上下一定的范围,并考虑目标可能的深度。简单地确定声纳探测深度,会严重减小声纳的有效搜索距离和搜索范围。利用射线模型仿真研究了深海中不同的声速剖面对吊放声纳探测距离的影响。通过分析深海不同声速剖面中的声传播特性,并对声纳、水声环境以及目标的模型化计算,利用射线模型仿真了几种不同声速剖面情况下吊放声纳的主动作用距离,最后分析了吊放声纳入水深度对深海目标主动作用距离的影响。仿真结果表明,改进方法可找到最佳的探测深度,并能够发挥声纳对目标探测性能,得到对不同环境下目标的最好探测。     

赣西浒坑钨矿床成矿岩体的磷灰石和锆石微量元素特征及其对成岩成矿的指示

赣西地区浒坑钨矿是我国华南钨、锡、铜多金属成矿区与中生代岩浆活动密切相关的典型矿床之一。对浒坑钨矿床中与成矿有关的白云母花岗岩开展了锆石U-Pb定年、磷灰石和锆石原位微量元素研究,结果表明：赋矿白云母花岗岩的成岩时代为（152.3±1.73）Ma;磷灰石具有特殊的“M”型REE球粒陨石标准化配分模式,富F和Mn,贫Cl和Mg;锆石具有高Th/U比值,REE球粒陨石标准化配分模式亏损LREE、富集HREE。锆石微量元素（Ce、U和Ti）温度计和氧逸度计结果表明,锆石形成于岩浆早期高温（800 ℃）和低氧逸度条件下。研究认为,浒坑赋矿花岗岩在演化初期经历了强烈的矿物结晶分异,矿床的形成可能与还原性高分异岩浆演化相关。     

Quantification of trace amounts of impurities in high purity cobalt by high resolution inductively coupled plasma mass spectrometry

An analytical method using high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) for rapid simultaneous determination of 24 elements (Be, Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn, Sb, Ba, Pt, Au, and Pb) in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCl. The matrix effects because of the presence of excess HCl and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the deter- mination were tested and discussed. The standard addition method was employed for quantitative analysis. The detection limits were 0.016-1.50 μg?g?1, the recovery ratios were 92.2%-111.2%, and the RSD was less than 3.6%. The method was accurate, quick, and convenient. It was applied to the determination of trace impurities in high purity cobalt with satisfactory results.     

金属材料中微量氢和氧的分析

叙述了惰性气氛熔化法测定金属材料中微量氢和氧的条件和方法。着重研究影响分析限的空白因素及降低空白的方法和分析限，制定出了Ｔｉ，Ｚｒ，Ｈｆ，Ｔａ，Ｎｂ，Ｗ，Ｍｏ，Ａｌ，Ｃｕ等及其合金中微量氢和氧的分析方法。     

催化动力学光度法测定痕量钒(Ⅴ)的研究

研究了在 p H=4及没食子酸存在下 ,微量钒 ( )催化溴酸钾氧化邻苯二胺的动力学条件 ,建立了催化动力学光度法测定痕量钒 ( )的新方法。方法的测定范围为 0～ 0 .0 2 5 μg· 2 5 m L- 1 ,检出限为 1.18× 10 - 6 g·L- 1 ,相对标准偏差为 4 .6 3% (n=10 ) ,线性回归方程为△ A=2 5 .6 6 c(μg· 2 5 m L- 1 ) - 0 .0 15 7(r=0 .9997) ,表观摩尔吸光系数ε4 6 0 nm=3.2 7× 10 7L· m ol- 1 · cm- 1 。该法灵敏度高 ,选择性好 ,直接应用于水样和食品样中痕量钒( )的测定 ,结果满意     

分光光度法测定微量表面活性剂在油/水体系中的分配系数

测定微量阴离子表面活性剂浓度的分光光度法被推广到测定油相中的微量阴离子表面活性剂浓度,进而用于表面活性剂在油/水体系中分配系数的测定.两种情形下氯仿层的吸光度只取决于测量体系中自由阳离子表面活性剂的浓度,因此可用单一阳离子的标准曲线作工作方程.用该法测定油相和水相中的阴离子表面活性剂浓度,工作方程斜率不同,测量下限分别可达2.5×10-5 mol·L-1和1×10-6mol·L-1.     

基于中红外QCL的痕量CO气体传感器

为了减少CO爆炸给国民经济造成的巨大损伤,提出了一种能够快速地监测环境空气中痕量CO的气体传感器。由于CO分子基频吸收谱带的吸收线强要比泛频带和组合频带的吸收线强高出2～3个数量级,选择激射中心波长为4.65μm中红外量子级联激光器（QCL）作为光源,同时再配合长光程Herriott气室提高了CO体积分数检测下限。同时,该传感器采用单光源双探测器差分光学结构,消除了电调制光源所带来的不稳定性。实验表明：该传感器CO体积分数检测下限为2×10-6,并且操作人员可以通过替换在不同波长下运行的中红外QCL来测量其它气体。