成都市浮尘物理与化学特征的初步研究

通过对成都市一环、二环路交叉处和纵贯市区人民路浮尘进行粒度、X射线衍射物相、元素组成等分析,研究了成都市浮尘的成分、元素含量、组合特征及其在空间的分布特征,对降低浮尘污染提出了初步建议.     

水化学指标表示裘布依公式的应用

从多矿物溶解化学动力学方程出发,推演并建立了由水化学指标表示的承压二维井流裘布依公式。结合水文地质、水文地球化学特征,列举了水文地质单元内不同区带、各种代表性矿物及相应组分化学指标的基本表达式。以山西省太原西峪煤矿所需解决的水文地质问题为例进行了定量研究与评价,其结果与已有的抽水试验资料接近,为矿井涌水量的评价开辟了一条新的道路。从事实上进一步论证了水化学指标表示裘布依公式的理论概括是正确的。     

电子探针化学测年方法

介绍含Th U Pb矿物电子探针化学测年方法的基本原理 ,并利用应用实例说明该方法在研究岩石形成年龄、构造热事件年代等方面的重要作用 ,最后简要评价该方法的优、缺点 ,并指出它的应用前景 ,认为电子探针化学测年方法将有可能在深源岩石包体年龄研究、含放射性元素矿床形成年代研究等方面大有作为 ,并使地质年代学研究更加精细化 ,有助于深入探讨复杂地质事件及其演化历程。     

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）。     

大兴安岭阿龙山地区流纹岩风化的地球化学特征

通过大兴安岭地区两个流纹岩风化剖面的研究发现，大兴安岭地区的岩石风化过程具有特殊性。风化过程分为两个阶段，即以化学风化为主导的基质风化阶段和以机械风化为主导的斑晶风化阶段，第二阶段显示出与正常风化剖面相反的风化趋势。低温和长冬使第二风化阶段延长，并呈现逆风化趋势。风化过程中Fe和Al始终处于流失状态。上述特征的产生是由原岩的结构及成分、气候因素和生态系统等多种因素作用的结果。     

煤岩显微组分热解气相色谱特征与化学结构剖析

煤结构是目前地球化学研究领域中的一个难点，但却具有极其重要的理论及实际意义，本文采用分步热解气相色谱技术将树皮体，镜质体和丝质体分解为分子量较小的可测定的有机化合物，在此基础上，据不同温度下热解产物的组成特征来还原显微组分的化学结构，实验结果表明，煤显微组分主要由四大类官能团组成，一是热稳定性较低的NOS杂原子官能团；二是脂族（脂链、脂环）结构；三是苯、烷基苯（甲苯、二甲苯）、萘等芳香族化合物，四是热稳定性很高的难以分解的稠环芳烃。上述四类化合物集中于显微组分的不同结构简单中，树皮体和镜质体结构单元外侧主要由热稳定性较低的杂原子化合物以及分子量较小的苯和烷基苯组成，而丝质体结构单元外侧则主要以短链脂族结构为主，三组分结构核部由热稳定性很高的难以分解的稠环芳烃组成。连结核部稠环芳烃与结构单元外侧杂原子等官能团的主要是热稳定性较高的脂链结构，煤显微组分热成烃主要按结构中各官能团键的强弱随热演化程度的加深依次脱除，生成油气，基本上属平行独立依次反应机制，亦“官能团脱除型”，此外，还包括少量的长链脂族结构裂解为短链脂肪烃的“解聚”过程。     

A Linear Programming Approach to Determine the Normative Composition of Sedimentary Rocks

The analysis of modal and normative composition of sedimentary rocks is widely used for studying their sources and tectonic settings. The normative calculation of the mineral composition of rocks in this study is formulated as a linear programming problem and is solved by means of the simplex method. This enables both simultaneous and successive subtraction of a set of basic minerals from a rock sample represented by its chemical composition {SiO₂...LOI}. Such an approach provides a more exact calculation of the contribution of basic minerals in the rock. This mathematical approach is used to study two representative sets of sandstones and fine-grained rocks from a Meso- to Neoproterozoic marginal basin of southeastern Siberia (Uchur–Maya region, Yakutia) and a Pennsylvanian-Lower Permian uplifted continental block in Colorado, USA. The calculated normative mineral compositions of the Siberian sandstones are consistent with the observed modal compositions. These sandstones vary from K- Feldspar rich arkoses at the base of the sequence (the Uchur Group, lower Riphean) to quartz arenites or lithic sandstones and wacke in transgressive successions of the middle-upper Riphean. Arkoses and quartz arenites are dominant in Meso- to Neoproterozoic Siberia. These samples represent craton interior uplifted basement and quartzose, recycled orogen provenance of a stable craton in Rodinia. There are higher but consistent discrepancies between the calculated and observed compositions for the Pennsylvanian to Lower-Permian arkoses and quartz arenites (Sangre de Cristo, Belden, and Maroon Formations). The differences between the predicted and observed mineralogy may be due to uncertainties in the modes in the matrix and cement of the sandstones. This normative program should supplement modal calculations and provide better genetic constructions, especially in case of matrix-rich sandstones.     

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).     

止水帷幕在高层建筑深基坑中的应用

某高层建筑基坑西侧紧邻一道河沟,水量较大,采取三重管高压摆喷帷幕止水[1～4],施工完成后通过监测,未发现渗漏、地下水位明显下降和周围建筑物沉降现象。