Application of AMD to the Determination of Cropprotection Agents in Drinking Water. Part III: Solid Phase Extraction and Affecting Factors Anwendung der AMD-Technik zur Bestimmung von Pflanzenbehandlungsmittel-Wirkstoffen im Trinkwasser. Teil III: Festphasenextraktion und ihre Einflußfaktoren

The more sensitive an analysis method the more care must be given to sample preparation. Solid phase extraction (SPE) onto RP 18 phases has established itself as a general purification and enrichment technique for trace components in aqueous samples. Various factors may thereby influence the recovery rate. For example, the ratio amount of sorbent and sample volume should be taken into account to avoid breakthrough of the investigated substance. Extracting phenylurea herbicides from drinking water, the ratio should be 1 g RP 18 sorbent per 1 L water sample. Concerning the flow rate for the fungicides procymidone, vinclozolin, and iprodione, the recovery rate decreases using higher flow rates than 3 or 6 mL/min. In the case of phenylurea herbicides, a flow rate of 10 or 14 mL/min showed best results. Even the coefficient of variation is below ± 5% at these flow rates. Furthermore, the company dependence should be considered because the recovery rate might differ by up to 40% using the nominally identical material. The same applies to the batch dependence of quality from the same company. The concentration of the eluate must also be monitored and carried out with great care to avoid decreasing the recovery rate. Considering these factors of influence, SPE is a very useful tool in sample preparation, particularly if an automated system is used.     

利用一维时间序列重建动力系统的初步研究

通过对月平均气温一维时间序列作相空间拓展,和假定相空间状态变量随时间的演化方程含有线性和非线性二次项,再根据拓展后的资料进行拟合,利用最小二乘法求出各项系数,保留其方差贡献大的项,以重建动力系统.实际计算结果表明,重建的低阶动力系统有可能对月平均气温所表征的短期气候演化过程的非线性特性作出描写.     

地球内部物质组成及其性质的研究

地球内部物质组成的研究涉及对地表现象的深入解释,与地球动力学、地球热结构及宇宙演化有着密切的关系.本文综述了这方面的研究结果及近期的进展,指出两种地幔模型的主要分歧点,讨论了地幔中的主要相变及与间断面的关系,对今后研究提出四点意见.     

H~+,Li~+,Mg~(2+)∥Cl~-—H_2O四元水盐体系在-10℃时的平衡溶解度相图

本文利用等温溶解度法测定了H~+,Li~+,Mg~(2+)//Cl~-—H_2O四元水盐体系在—10℃±0.1℃时的溶解度并绘制了等温相图。相图由HCl·MgCl_2·7H_2O、MgCl_2·8H_2O、HCl·6H_2O和LiCl·2H_2O四个相区构成,只有一个零变量点I:LiCl·2H_2O+MgCl_2·6H_2O+HCl·MgCl_2·7H_2O+L_(?)利用坐标变换和直线外推法,对溶解度数据进行处理后,用湿渣结线法解决了低温平衡固相较难确定的问题。     

三元体系Li~+,Mg~(2+)∥SO_4~(2-)—H_2O 25℃相关系及溶液物化性质的研究

研究了三元体系Li~+,Mg~(2+)∥SO_4~(2-)—H_2O在25℃时的相关系和平衡液相的密度、粘度、折光率、电导等物化性质,该体系为简单共饱型,两段溶解度曲线对应于体系的两种原始组份Li_2SO_4·H_2O和MgSO_4·7H_2O的结晶区,无复盐和固溶体形成,亦无脱水作用发生,应用电解质溶液Pitzer模型检测该体系25C的溶解度,并用经验或半经验公式对平衡液相的密度和折光率进行了理论计算,计算值与实验值非常接近。     

全波震相分析的应用

全波震相分析法是以弹性波传播理论为基础,以现代数字技术为手段,对地震波进行全面综合分析的理论和方法.它既包括对单一分量震波观测记录中的各种震相的识别、确认和分析,又包括对多分量震波记录的合成、分析和图示.全波震相分析法涉及震源、射线路径、初动、走时、振幅、波形、时域和空域的瞬态谱、质点振动矢量等诸多方面,因而能更全面地揭示地震波场与地下介质之间的关系.本文以实例展示在不同领域的研究中全波震相分析的应用情况.全波震相分析法为实现多种波型的联合应用奠定了理论基础,并提供了新的方法.     

精密引潮位展开及某些诠释

作者再次改进了引潮位展开,潮波振幅给到小数后第六位,共3070个潮波.文中论述了引潮位展开的精度,同时给出为了保证潮汐计算的高精度而所需引入的各项改正及其说明.     

氧化镍、二氧化钛高压相变及电导率压力效应

采用金刚石对顶砧压腔静高压技术，对氧化镍、二氧化钛在０-３２ＧＰａ压力范围内的电导率进行了测量．结果表明，电导率－压力关系曲线上的一些特征点与同一物质的高压相交点具有一致性．     

东台吉乃尔盐湖卤水的相化学研究（Ⅱ）—冬夏季卤水蒸发实验

为了研究东台吉乃尔盐湖卤水蒸发时的相化学，确定钾、镁和锂盐的结晶特性，在实验室内２５℃等温蒸发实验基础上和自然条件下进行了冬夏季日晒蒸发试验．东台吉乃尔盐湖卤水是由氯化钠饱和的多组分复杂体系构成的．卤水中存在的离子是Ｎａ＋、Ｋ＋、Ｍｇ２＋、Ｌｉ＋、Ｃａ２＋、Ｂ３＋、ＳＯ４２－和Ｃｌ－．试验数据与Ｎａ＋、Ｋ＋、Ｍｇ２＋Ｃｌ－、ＳＯ４２－ＫＨ２Ｏ五元体系介稳平衡数据进行了讨论和比较．Ａｕｔｅｎｒｉｅｔｈ相图被用来表示各数据间的关系和证明冬夏季蒸发时结晶行为的差别．     

Nonequilibrium thermodynamics of pressure solution

This paper is concerned with the thermodynamic theory of solution and precipitation processes in wet crustal rocks and with the mechanism of steady pressure-solution slip in contact zones, such as grain-to-grain contacts, fracture surfaces, and permeable gouge layers, that are infiltrated by a mobile aqueous solution phase. A local dissipation jump condition at the phase boundary is fundamental to identifying the thermodynamic force driving the solution and precipitation process and is used here in setting up linear phenomenological relations to model near-equilibrium phase transformation kinetics. The local thermodynamic equilibrium of a stressed pure solid in contact with its melt or solution phase is governed by Gibbs's relation, which is rederived here, in a manner emphasizing its independence of constitutive assumptions for the solid while neglecting surface tension and diffusion in the solid. Fluid-infiltrated contact zones, such as those formed by rough surfaces, cannot generally be in thermodynamic equilibrium, especially during an ongoing process of pressure-solution slip, and the existing equilibrium formulations are incorrect in overlooking dissipative processes tending to eliminate fluctuations in superficial free energies due to stress concentrations near asperities, defects, or impurities. Steady pressure-solution slip is likely to exhibit a nonlinear dependence of slip rate on shear stress and effective normal stress, due to a dependence of the contact-zone state on the latter. Given that this dependence is negligible within some range, linear relations for pressure-solution slip can be derived for the limiting cases of diffusion-controlled and interface-reaction-controlled rates. A criterion for rate control by one of these mechanisms is set by the magnitude of the dimensionless quantityk/2C _pD, wherek is the interfacial transfer coefficient, is the mean diffusion path length,C _p is the solubility at pressurep, andD is the mass diffusivity.