用双孔热解石墨管原子吸收法测定微量金

石墨炉原子吸收法在对化探样品微量金的测试过程中存在因载气进入而使待测样品溅出的问题。利用自制的双孔热解石墨管代替普通石墨管可解决上述问题。通过大量的实验证明,仪器在最佳工作条件下,硫脲介质浓度10g·l-1、解脱时间40min时,获得检出限0 10×10-9、加标回收率为98 4%～103 7%的分析结果。     

抽放瓦斯定向钻孔施工技术的研究

介绍了抽放瓦斯定向钻孔施工技术的主要设备、钻具及仪器，组合钻具及钻进工艺参数，并通过几个工程实例，说明了该项技术的应用效果。     

大青山古元古代变质卯独庆金矿床地质特征

九八年以来,在内蒙大青山地区古元古界二道洼群地层中陆续发现了一批以卯独庆金矿为典型代表的层控特征十分明显的新类型金矿。二道洼群是一套大陆裂谷盆形碎屑岩建造,以杂砂岩、碳酸岩、砂质泥岩、粘土岩为主,上部夹中基性火山岩建造;变质从低绿片岩相到低角闪岩相,变形复杂。金矿体产于固定的层位二道洼群红山沟组的云母片岩和大理岩中,受顺层滑脱作用形成糜棱岩化带控制,矿化均匀,厚度大,平均品位可达6×10-6以上,最高达23×10-6。矿石矿物成分主要有银金矿、黄铁矿、黄铜矿、方铅矿等。成矿时代早于中元古代。而且该类金矿物化探异常显示良好,Au、Ag、Cu、Pb四种元素为矿体晕元素组合。这些特征都表明其成矿作用具特殊性,与产于内蒙新太古界乌拉山群及色尔腾山群中的金矿类型完全不同。因此,有必要对该类金矿的成矿机制及成矿时代进行重新认识。     

单道扫描电感耦合等离子体发射光谱法测定珊瑚礁中主量和微量元素

建立了用单道扫描电感耦合等离子体发射光谱法测定珊瑚礁中主量和微量元素的方法。珊瑚礁样品经酸溶解后,直接进行Ca、Mg、K、Na、V、Sr、Ba、Co、Ni、Pb、Li、Rb的测定,方法检出限为0.0004～0.1mg/L,精密度RSD<5%(n=6),样品的加标回收率为97%～105%。测定w(CaO)为50%的样品,结果与传统的EDTA容量法相符。方法经碳酸盐岩石国家一级标准物质验证可行,已用于大批量的珊瑚礁样品的测定。     

底质不连续面类型、成因及遗迹学特征

底质不连续面是沉积作用中断时所形成的一种地层界面。根据底质的粘结程度可将底质不连续面划分为两大类：固底不连续面和硬底不连续面。固底不连续面中的简单停积面依靠沉积序列的变化来识别，界面上、下的生物地层带是连续的；而复成停积面上、下的生物地层带不连续。在硬底不连续面中，硬底的上、下地层属于同一个沉积体系，而继承性岩底的上、下地层则属于不同的沉积体系，其间发生过重大的沉积间断。根据底质控制的Glossifungites遗迹相和Trypanites遗迹相可以有效地识别各类不连续面并解释其成因。三种类型的不连续面具有层序地层学意义：①侵蚀性不连续面，包括低水位侵蚀面（LSE）和海进侵蚀面（TSE）；②无沉积间断面；③沉积性不连续面（凝缩段）。     

Laser Ablation ICP-MS Analysis of Geological Materials Prepared as Lithium Borate Glasses

A simple, rapid and precise method is described for determining trace elements by laser ablation (LA)-ICP-MS analysis in bulk geological materials that have been prepared as lithium borate glasses following standard procedures for XRF analysis. This approach reliably achieves complete sample digestion and provides for complementary XRF and LA-ICP-MS analysis of a full suite of major and trace elements from a single sample preparation. Highly precise analysis is enabled by rastering an ArF excimer laser (λ= 193nm) across fused samples to deliver a constant sample yield to the mass spectrometer without inter-element fractionation effects during each analysis. Capabilities of the method are demonstrated by determination of twenty five trace elements (Sc, Ti, V, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Hf, Ta, Pb, Th and U) in a diverse range of geological reference materials that includes peridotites, basalts, granites, metamorphic rocks and sediments. More than 90% of determinations are indistinguishable from published reference values at the 95% confidence level. Systematic bias greater than 5% is observed for only a handful of elements (Zr, Nb and U) and may be attributed in part to inaccurate calibration values used for the NIST SRM 612 glass in the case of Zr and Nb. Detection limits for several elements, most notably La, are compromised at ultra-trace levels by impurities in the lithium borate flux but can be corrected for by subtracting appropriate procedural blanks. Reliable Pb analysis has proved problematic due to variable degrees of contamination introduced during sample polishing prior to analysis and from Pt-crucibles previously used to fuse Pb-rich samples. Scope exists for extending the method to include internal standard element/isotope spiking, particularly where integrated XRF analysis is not available to characterise major and trace elements in the fused lithium borate glasses prior to LA-ICP-MS analysis.     

A Reappraisal of Rb, Y, Zr, Pb and Th Values in Geochemical Reference Material BHVO-1

The geochemical reference material BHVO-1 was analysed by a variety of techniques over a six year period. These techniques included inductively coupled plasma-mass spectrometry and atomic emission spectroscopy (ICP-MS and ICP-AES, respectively), laser ablation ICP-MS and spark source mass spectroscopy. Inconsistencies between the published consensus values reported by Gladney and Roelandts (1988, Geostandards Newsletter) and the results of our study are noted for Rb, Y, Zr, Pb and Th. The values reported here for Rb, Y, Zr and Pb are generally lower, while Th is higher than the consensus value. This is not an analytical artefact unique to the University of Notre Dame ICP-MS facility, as most of the BHVO-1 analyses reported over the last ten to twenty years are in agreement with our results. We propose new consensus values for each of these elements as follows: Rb = 9.3 ± 0.2 μg g-1 (compared to 11 ± 2 μg g-1), Y = 24.4 ± 1.3 μg g-1 (compared to 27.6 ± 1.7 μg g-1), Zr = 172 ± 10 μg g-1 (compared to 179 ± 21 μg g-1), Pb = 2.2 ± 0.2 μg g-1 (compared to 2.6 ± 0.9 μg g-1) and Th = 1.22 ± 0.02 μg g-1 (compared to 1.08 ± 0.15 μg g-1).     

对目前岩石“全曲线”测试的若干看法

从电液伺服岩石压力试验机工作机理的角度,对目前岩石应力-应变全过程曲线(以下简称“全曲线”)测试中的一些问题进行了分析,提出了自己的看法,目的是为了解决“全曲线”测试的2个问题,即如何测出“全曲线”;如何使测出的“全曲线”真实反映岩石的力学特性,并将其用到工程中。     

河北省黄壁庄水库坝基渗漏单井示踪试验研究

以河北省黄壁庄水库副坝坝基的渗漏塌坑为例，利用“九五”国家重点科技成果推广项目“智能化地下水动态参数测量仪”在天然流场下，测量出水库自然渗漏量地下水的渗透流速流向、垂直向流速流向，每米含水层的渗透系数等工程必须的水文地质参数。确定性地诊断和检测出黄壁水库坝基渗漏隐患出现的具体位置和高程，从而为大坝的渗漏处理和安全处理提供详细的现场测量数据。     

Column Amounts of ClONO2, HCl, HNO3, and HF from Ground-Based FTIR Measurements Made Near Kiruna, Sweden, in Late Winter 1994

During SESAME phase I ground-based FTIR measurements were performed atEsrange near Kiruna, Sweden, from 28 January to 26 March 1994. Zenith columnamounts of ClONO₂, HCl, HF, HNO₃,O₃, N₂O, CH₄, and CFC-12 werederived from solar absorption spectra. Time series of ClONO₂and HCl indicate a chlorine activation at the end of January and around 1March. On 1 March a very low amount of HCl of 2.09times; 10¹⁵molec. cm^-2 was detected, probably caused by a second chlorineactivation phase starting from an already decreased amount of HCl. The ratioof column amounts of HCl to ClONO₂ decreased inside the vortexfrom about 1 in January to 0.4 in late March compared to values of about 2outside the vortex. Although the Arctic stratosphere was rather warm in winter1993/94 and PSCs occurred seldom, chlorine partitioning into its reservoirspecies HCl and ClONO₂ changed during that winter andClONO₂ is the major chlorine reservoir at the end of thewinter as in cold winters like 1991/92 and 1994/95.