柴东欧南凹陷石炭系烃源岩有机质富集的影响因素

柴达木盆地东部地区欧南凹陷是石炭系油气运聚成藏的有利构造单元,具有一定勘探潜力,但对有机质富集机理认识不清导致对优质烃源岩分布的预测缺乏有效指导,制约了油气勘探进程.基于地球化学分析、XRD、SEM等分析测试,对石炭系烃源岩矿物组分、 有机质丰度、 干酪根类型、 热演化程度、 形成环境、TOC与主要矿物关系等进行了综合...     

毛细管合成包裹体在激光拉曼探针测定包裹体盐度中的应用

盐度是流体包裹体重要的参数之一,利用激光拉曼探针可以快速、准确地测定包裹体盐度,而标准样品的制备是保证该方法准确性的关键。毛细管合成包裹体技术是一种新型的标准样品制备方法,本文利用该方法,制备了不同组成的H₂O-NaCl样品,并以此建立了测定包裹体盐度的标准曲线。显微测温结果表明,毛细管合成包裹体标准样品盐度的准确性可以达到±0.5%,利用石英和石盐中的合成包裹体对标准曲线进行了检验,结果表明利用标准曲线测定包裹体盐度,测量值与理论值的误差在1%以内。应用该方法制备的标准样品具有操作简便、快捷、样品尺寸与地质样品相类似等特点,兼具了矿物中合成包裹体以及石英试管或玻璃瓶制备标准样品的优势。     

重量法测定岩石矿物中二氧化硅的几种凝聚剂

文章对十六烷基三甲基溴化铵、聚环氧乙烷、聚乙二醇（４００和６０００）、甲基纤维素和聚乙烯醇等６种凝聚剂在重量法测ＳｉＯ２过程中凝聚硅酸的效果进行了试验，这些操作较动物胶法方便、省时，测定标准样品结果与推荐值相符。     

测定硅灰石制得多孔SiO2粉体粒径的分散剂选择研究

考察了几种不同类型表面活性剂对一种气相白炭黑的分散效果。经比较研究发现：吐湿－80和六偏磷酸钠的分散效果较类似且较好，对此进行了讨论并选择六偏磷酸钠作为分散剂测试了由硅灰石制制得的多孔SiO2粉体的颗粒粒径。初步确定，该多孔SiO2粉体作为填料可用于反光塑料制品中。     

硅的生物地球化学循环研究进展

生命元素硅在陆地生态系统和水生生态系统中都扮演着重要的角色。它的生物地球化学循环与全球碳循环和全球气候交化密切相关。因此,近年来逐渐成为研究的热点。本文概述了近年来国内外有关硅的生物地球化学循环的研究进展,包括陆地和海洋中硅的生物地球化学循环过程及人类活动对硅循环的影响等方面,指出日前研究中存在的问题,展望了研究的重点。     

Surface Charge Concentrations on Silica in Different 1.0 M Metal-Chloride Background Electrolytes and Implications for Dissolution Rates

The empirical rate laws formulated to describe the dissolution rates of oxide minerals include the surface charge concentration that results from the protonation and deprotonation of surface functional groups. Previous experiments on quartz and silica have shown that dissolution rates vary as a function of different background electrolyte solutions, however, such experiments are often conducted at elevated temperatures where it is difficult to estimate surface charge along with the dissolution rates. In the present study we measuresurface charge concentrations for silica in different electrolyte solutions at 298 K in order to quantify the extent to which the different counterions could affect the dissolution rates through their influence on the surface charge concentrations. The experimental solutions in the electrolyte series: LiCl, NaCl, KCl, RbCl, CaCl₂, SrCl₂ and BaCl₂ were prepared to maintain a constant metal concentration of 1.0 M. For the alkali-metal chlorides, the surface charge concentrations correlate with the size of the hydrated alkali metal, consistent with the idea that these counterions affect charge via outer-sphere coordination that shield proton surface complexes from one another. The reactivity trend for alkaline-earth cations is less clear, but the data demonstrate distinct differences in the acid-base propertiesof the silica surface in these different electrolytes. We then discuss how these trends are manifested in the rate equations used to interpret dissolution experiments.     

Mineralogical and Geochemical Characteristics of the Utanobori Gold Deposit in Northern Hokkaido,Japan

The Utanobori gold deposit is a low‐sulfidation, epithermal vein‐type deposit located in northern Hokkaido, Japan. The deposit is hosted by conglomerate, sandstone, and tuff of the Middle to Late Miocene Esashi Formation. These rocks were hydrothermally altered. Silica sinters and quartz‐adularia veins are common in the deposit. The quartz‐adularia veins either contain a ginguro band, which corresponds to the main gold‐bearing vein (Type 1 Veins), or do not contain a ginguro band but contain minor adularia (Type 2 Veins). Type 1 Veins are divided into three stages with 12–14 substages. Ore minerals identified include electrum, naumannite, chlorargyrite, bromargyrite, an unidentified Fe‐Sb mineral, and an Fe‐(Sb)‐As mineral. These ore minerals formed in the main mineralization stages I (bands I‐b and I‐d) and II (band II‐a). Scanning electron microscopy with cathodoluminescence images show that cathodoluminescence‐dark microcrystalline quartz exhibiting colloform (ghost‐sphere) texture is closely associated with ore minerals in the Type 1 Vein and Type 2 Vein, and the Al and K contents of such quartz are commonly >1000 ppm. This indicates that the ore minerals were crystallized from alkaline, silica‐saturated fluids at temperatures <200°C, which initially deposited amorphous silica that was recrystallized to microcrystalline quartz. The average Au content of electrum is 52.5 at% Au (n = 10), 65.7 at% Au (n = 20), and 55.5 at% Au (n = 5) in bands I‐b, I‐d, and II‐a, respectively, of Type 1 Veins. The δ³⁴S_CDT values of two fine‐grained disseminated pyrites in the altered conglomerate and bedded tuff in the argillic altered zone are ?4.3 and ?4.2‰. Ar‐Ar dating on adularia yielded 13.6 ± 0.06 Ma, 13.6 ± 0.07 Ma, and 13.6 ± 0.06 Ma for the stages I, II, and III of the Type 1 Vein, respectively. K‐Ar ages determined on adularia in the silica sinter and on whole‐rock of glassy rhyolite of the Esashi Formation are 15.0 ± 0.4 Ma and 14.6 ± 0.4 Ma, respectively. These radiometric ages indicate that silica sinter associated with the rhyolitic volcanic rocks formed prior to the main gold mineralization.     

Dolomite–silica stromatolites in Miocene lacustrine deposits from the Duero Basin, Spain: the role of organotemplates in the precipitation of dolomite

This research provides an ancient analogue for biologically mediated dolomite precipitation in microbial mats and biofilms, and describes the involvement of highly structured extracellular polymeric secretion (EPS) templates in dolomite nucleation. The structure of EPS is shown to match the hexagonal–trigonal lattice geometry of dolomite, which favoured the epitaxial crystallization of dolomite on the organic substrate. This structure of EPS also matches the arrangement of silica nanospheres in opal, which further accounts for the organically‐templated formation of opal enabling the non‐replacive co‐existence of dolomite and silica. The study is focused on a 50 m thick dolomite succession that is exposed in central areas of the Tertiary Duero Basin and was deposited in a mudflat‐saline lake sedimentary complex during the Middle to Late Miocene (9 to 15 Ma). In the intermediate intervals of the succession, poorly indurated dolomite beds pass gradually into silica beds. On the basis of sedimentological, compositional, geochemical and petrographic data, silica and dolomite beds have been interpreted as mineralized microbial mats. The silica beds formed in marginal areas of the lake in response to intense evaporative concentrations; this resulted in the rapid and early precipitation of opal. Silicification accounted for the exceptional preservation of the microbial mat structure, including biofilms, filamentous and coccoid microbes, and EPS. Extracellular polymeric secretions have a layered structure, each layer being composed of fibres which are arranged in accordance with a reticular pattern, with frequent intersection angles at 120° and 60°. Therefore, the structure of EPS matches the lattice geometry of dolomite and the arrangement of silica nanospheres in opal. Additionally, EPS binds different elements, with preference to Si and Mg. The concurrence of suitable composition and surface lattice morphologies in the EPS favoured the crystallization of dolomite on the substrate. In some cases, dolomite nucleation took place epicellularly on coccoid micro‐organisms, which gave way to spheroid crystals. Organic surfaces enable the inorganic mineral precipitation by lowering the free energy barrier to nucleation. Most of the microbial mats probably developed on the lake floor, under sub‐aqueous conditions, where the decomposition of organic matter took place. The subsequent formation of openly packed dolomite crystals, with inter‐related Si‐enriched fibrils throughout, is evidence for the pre‐existence of fibrillar structures in the mats. Miocene dolomite crystals are poorly ordered and non‐stoichiometric, with a slight Ca‐excess (up to 5%), which is indicative of the low diagenetic potential the microbial dolomite has towards a more ordered and stoichiometric structure; this confirms that microbial imprints can be preserved in the geological record, and validates their use as biosignatures.     

Solubility of silica polymorphs in electrolyte solutions, II. Activity of aqueous silica and solid silica polymorphs in deep solutions from the sedimentary Paris Basin

Activity coefficient for aqueous silica in saline waters and brines from the Paris Basin was calculated using Pitzer's specific interaction model. Quartz and chalcedony are the only reported authigenic silica minerals in the Dogger aquifer of the Paris Basin (France). However, the measured silica concentrations fall between those of these two phases. The silica concentrations measured in Dogger fluids seem to be controlled by a microcrystalline quartz phase with a grain size computed to be about 20 nm. Studies have shown that pressure can preserve small grain size for a long time at the geological scale. The effective mechanism of pressure action is probably linked to the fact that pressure simultaneously favours dissolution at the grain-contact inducing a quartz supersaturation and prohibits the increase in size of reprecipitated microcrystalline quartz grains. This hypothesis is supported by other studies reported in the literature. The proposed model, which incorporates silica mineralogy and a precise calculation of aqueous silica activity, allows us to explain measured silica concentrations in the deep sedimentary solutions of the Dogger aquifers. In the Keuper brines, silica solubility can in most cases be explained by an equilibrium with either chalcedony or quartz. Another application of the present work is shown by an example, where we examined the importance of precisely evaluating the activity coefficient in basin characterisation, as the goal of reservoir characterisation is to describe the spatial distribution of petrophysical parameters such as porosity, permeability, and saturations.     

纳克级铅同位素分析中硅胶-高铼酸发射剂体系的建立

核取证分析中需要实施纳克级（ng）铅的同位素全谱分析,质谱测量中要求铅的电离效率较高（大于10^-3）。传统硅胶-磷酸技术多用于微克级（μg）铅分析,电离效率一般为10^-4~10^-3;尽管后来发展的硅胶-硼酸技术可以得到10^-3以上的发射效率,但是由于铅在电离过程中存在离子流反复升高-衰减的过程,导致离子流发射不稳定,质谱测量条件难以掌握。本文改进了传统的硅胶发射剂,建立了一种新型硅胶加载体系——硅胶-高铼酸体系。与硅胶-硼酸技术相比,采用硅胶-高铼酸体系可显著提高铅的发射效率并获得稳定的离子流。对于1 ng铅的同位素质谱全谱测量,²⁰⁴Pb/²⁰⁶Pb、²⁰⁷Pb/²⁰⁶Pb、²⁰⁸Pb/²⁰⁶Pb的相对标准偏差分别为0.4%、0.2%和0.1%,测试精度优于采用其他硅胶技术。通过实验比较了硅胶-高铼酸体系与多种传统硅胶发射剂体系对铅离子流的发射效果,优化了硅胶试剂用量为0.5~3.0 μL,采用“夹心饼干”的涂样顺序,对1~100 ng铅样品的发射效率达到6.0×10^-3~4.6×10^-2,比传统硅胶-磷酸体系的发射效率（10^-4~10^-3）高了近10倍,与硅胶-硼酸技术的发射效率相当（10^-3~10^-2）,但铅离子发射更为稳定。本文建立的硅胶-高铼酸体系在测量精度上可满足核取证研究中铅作为地域指示剂的需求。