骨灰－伊利石－高岭石体系假相图的研究

采用骨灰、伊利石粘土和高岭石粘土作为端元组分，并根据ＤＴＡ、热台显微镜、互ＲＤ方法测定的数据，组成了这个三元体系的假相图。依据假相图讨论了该体系的热相变特征以及有关骨灰瓷工艺学问题。     

高岭石-伊利石-透辉石体系假相图

采用较纯透辉石岩、高岭石粘土和伊利石粘土作为端元组分,并根据用 DTA、热台显微镜、XRD 方法测定的数据组成了三元体系的假相图。根据假相图说明了有关陶瓷工艺学和变质岩岩石学的一些问题。     

硅灰石、透辉石在陶瓷中的基本反应和作用

本文以硅灰石和高岭石、透辉石和高岭石为端元组分,推导了二元假相图。根据这两个假相图,提出了四个基本固相反应。用这些基本反应以及硅灰石、透辉石的矿物学性质,说明了它们对陶瓷坯体工艺性能的作用。     

凹凸棒土抗高温钻井液的配方实验研究

针对现下钻探深井对抗高温钻井液的要求,在实验室内对聚合物增粘降滤失剂以及钻井液用粘土进行优选,建立抗高温钻井液的配方体系。该体系在经历200 ℃、16 h的热滚实验之后,依然保持良好的体系稳定性以及较低的滤失量。     

金属离子对粘土土工性状影响的实验

在正交实验设计的基础上,通过大量的室内实验,对粘土吸附性的影响因素加以分析,为金属离子影响下的粘土土工性状研究奠定基础。在粘土吸附性的基础上,对粘土吸附离子后的基本土工特性进行实验研究,得出了粘土土工特性的变化趋势。结果表明:在单离子体系中粘土对离子的吸附量明显大于混合离子体系中对该离子的吸附量;在多离子体系中,则表现为高价离子具有更强的竞争力;粘土的塑性指数基本是随离子含量的增加而增大;粘土强度随着离子总含量的增高而逐渐降低。      

红粘土在岩土工程应用中的若干问题

本文探讨红粘土在岩土工程应用中的一些代表性问题,如塑性图、红粘土分类、膨胀势与试验研究处理以及一些工程隐患的发生、发展。     

地洼盆地砂岩铜矿床的 构造－流体－成矿体系及演化

我国南方地洼盆地构造演化、流体演化和砂岩铜矿成矿作用三者之间具有密切的关系,处于一个统一的系统之中。盆地早中期的裂陷、坳陷作用及热构造活动导致了富铜矿源层的形成、大气降水的深循环和水/岩相互作用、并形成中高温、压、高盐度的热卤水含铜流体。在构造－流体－砂岩铜矿成矿体系的演化中,构造演化制约了含铜流体的演化和砂岩铜矿的成矿作用,而主要发生于盆地演化的晚期。     

CSR钻探方法简介(下)

二、钻具组合CSR钻进根据地层条件可采用三种钻具组合，结合图8分述如下：1．取心钻具，如图8是在双壁钻杆下端直接连接一开式镶嵌钻头14（OPEN FACE INSERTBIT）适用于流砂，粘土及第四系覆盖层钻进。使用这种钻具钻进粘土层时，常可取出一段一段的粘土塞即柱状粘土心，这时，该方法便可称之为“中心取心”（CENTRUL CORE RECOVERY）。     

认广西红粘土的胀缩性能

文章从由碳酸盐岩深余堆积形成的红粘土引起产生的地裂、房裂等不良工程地质现象入手,以大量的实验资料为基础,指出广西红粘土的胶粒含量,可塑性指标高,具有较强的吸附能力和较强的亲水性,自由膨胀率接近或等于２７％。论述了红粘土液限和逆限值在塑性图上的分布规律与一般膨胀土的分布规律相吻合,这种粘土应属于弱至中等级膨胀性粘土,并以收缩变表为其主要特征。     

浅析福建省天湖山煤矿区上姚井田主要含煤段 (P1t1)沉积体系、聚煤环境及其含煤性

从砂岩体的微观特征及粘土岩的染色特征(如碎屑沉积岩、粘土岩等特征)切入,分析了童子岩组一段的岩性相、沉积组合以及相的空间配置.提出了滨海碎屑沉积体系、潮坪沉积体系、障壁岛-泻湖沉积体系和浅海沉积体系为天湖山煤矿区上姚井田主要含煤段(P1t1)的沉积环境,并探讨了其聚煤规律.     

Evidences of felsic volcanism and hydrothermal activities from clays associated with the Palaeoproterozoic Porcellanite Formation of the Vindhyan Supergroup,Central India

Chemico-mineralogical attributes of authigenic clays associated with the altered volcanic tuffs that occur in the Palaeoproterozoic Porcellanite Formation contain evidences of hydrothermal alteration and diagenetic processes in a marine environment. Previous sedimentological and geochemical studies on Porcellanite Formation were restricted to the Chopan area, but, the details related to provenance, nature and source of volcanism archived in these clays have not been ascertained. In order to understand these aspects, present study on these authigenic clays were carried out. Clay minerals represent dominance of illite with subordinate amount of montmorillonite. Moreover, low abundance of kaolinite is also noticed. The illite fibers and plates associated with the kaolinite indicate illitization. The kaolinite to illite transformation is favoured by incorporation of K⁺ ions, derived from the K-feldspar dissolution and its overgrowth. Major oxide contents of these clays and their ratios when plotted over diagrams marked with standard illite, kaolinite, smectite and chlorite compositional fields show clustering within or close to the illite field. Thermodynamic components calculated for these clays when plotted over AR₂³⁺AlSi₃O₁₀(OH)₂ − R₂³⁺Si₄O₁₀(OH)₂ − AR²⁺R³⁺Si₄O₁₀(OH)₂ ternary diagram, data plots lie within the illite, mixed layer I/S and smectite fields. Binary major oxide data plots between bulk rock and authigenic clay compositions showed felsic affinity. Montmorillonite and illite predominated in the eastern and western marginal areas of the Vindhyan Basin, respectively. However, former resulted from the hydrothermal alteration of volcanic glass associated with the ferruginous breccia and altered tuffs and remnants of the volcanic vents, whereas, later is associated with the tuffaceous beds. Owing to the adsorption, Ba, Rb and Sr is enriched in clays comparing to the bulk rock composition. Low (< 15 ppm) Sc values suggested major contribution from the felsic component. Also, low Rb/Sr and Th/U values revealed moderate insitu weathering. The dominance of K-feldspar alteration and insitu weathering is also evident from clustering of clay data plots in the A-CN-K ternary diagram. Pronounced negative Eu anomaly together with higher LREE/HREE values associated with these clay minerals implied proximity to source and their possible derivation from the silicified felsic tuffs available in the provenance.     

Enrichment of U-Re-V-Cr-Se and rare earth elements in the Late Permian coals of the Moxinpo Coalfield,Chongqing, China: Genetic implications from geochemical and mineralogical data

Rare metals in coal deposits have attracted much attention in recent years because of their potential economic significance. This paper reports the abundance and enrichment origin of rare metals in the Late Permian coals (K1 and K2 Coals) of the Moxinpo Coalfield, Chongqing, southwestern China. The K1 Coal is characterized by highly-elevated concentrations of U-Re-V-Cr-Se and Nb(Ta)-Zr(Hf)-REE assemblages; the latter assemblage is also enriched in the K2 Coal. The high temperature ash (815 °C) of the K1 Coal is enriched in V, Cr, Se, Re, U and REE; the ash of the K2 Coal, and also the floor strata of each seam, are enriched in REE, potentially making all of the units economically viable sources for these elements.The minerals in the K1 Coal are mainly represented by kaolinite, illite and mixed-layer illite/smectite, and pyrite, while the minerals in the K2 Coal consist mainly of kaolinite and tobelite [(NH₄,K)Al₂(AlSi₃O₁₀)(OH)₂]. Authigenic roscoelite [K(V^3 +,Al)₂(AlSi₃O₁₀)(OH)₂] is commonly observed in the K1 Coal under the SEM, and was probably formed by interaction of kaolinite with V derived from permeating U-Re-V-Cr-Se-rich solutions during early diagenesis. The tobelite enriched in the K2 Coal was formed by reaction between kaolinite already present in the coal and NH^4 + derived from decomposition of the organic matter during hydrothermal alteration at a relatively high temperature.The mafic tuffs directly underlying the K1 Coal and containing limestone residual breccias not only served as the substrate for coal accumulation but also as the source of sediment from the uplifted areas around the coal basin. The latter is indicated by low Al₂O₃/TiO₂ ratios (from 10.09 to 14.24), positive Eu anomalies enrichment of medium rare earths (relative to upper continental crust), and detrital calcite of terrigenous origin. The highly-elevated concentrations of U-Re-V-Cr-Se assemblages in the coal were derived from exfiltrational hydrothermal solutions and were then deposited in a euxinic environment. The terrigenous materials in the K2 Coal, however, were derived from felsic-intermediate rocks at the top of the Kangdian Upland, although the elevated concentrations of Nb(Ta)-Zr(Hf)-REE assemblages are attributed to the input of hydrothermal solutions.     

Influence of soil minerals on chromium(VI) reduction by sulfide under anoxic conditions

The effects of soil minerals on chromate (Cr^VIO₄ ^2-, noted as Cr(VI)) reduction by sulfide were investigated in the pH range of 7.67 to 9.07 under the anoxic condition. The examined minerals included montmorillonite (Swy-2), illite (IMt-2), kaolinite (KGa-2), aluminum oxide (γ-Al₂O₃), titanium oxide (TiO₂, P-25, primarily anatase), and silica (SiO₂). Based on their effects on Cr(VI) reduction, these minerals were categorized into three groups: (i) minerals catalyzing Cr(VI) reduction – illite; (ii) minerals with no effect – Al₂O₃; and (iii) minerals inhibiting Cr(VI) reduction- kaolinite, montmorillonite, SiO₂ and TiO₂ . The catalysis of illite was attributed primarily to the low concentration of iron solubilized from the mineral, which could accelerate Cr(VI) reduction by shuttling electrons from sulfide to Cr(VI). Additionally, elemental sulfur produced as the primary product of sulfide oxidation could further catalyze Cr(VI) reduction in the heterogeneous system. Previous studies have shown that adsorption of sulfide onto elemental sulfur nanoparticles could greatly increase sulfide reactivity towards Cr(VI) reduction. Consequently, the observed rate constant, k _obs, increased with increasing amounts of both iron solubilized from illite and elemental sulfur produced during the reaction. The catalysis of iron, however, was found to be blocked by phenanthroline, a strong complexing agent for ferrous iron. In this case, the overall reaction rate at the initial stage of reaction was pseudo first order with respect to Cr(VI), i.e., the reaction kinetics was similar to that in the homogeneous system, because elemental sulfur exerted no effect at the initial stage prior to accumulation of elemental sulfur nanoparticles. In the suspension of kaolinite, which belonged to group (iii), an inhibitive effect to Cr(VI) reduction was observed and subsequently examined in more details. The inhibition was due to the sorption of elemental sulfur onto kaolinite, which reduced or completely eliminated the catalytic effect of elemental sulfur, depending on kaolinite concentration. This was consistent with the observation that the catalysis of externally added elemental sulfur (50 μM) on Cr(VI) reduction would disappear with a kaolinite concentration of more than 5.0 g/L. In kaolinite suspension, the overall reaction rate law was:

Diagenesis and Very Low‐grade Metamorphism of the Upper Permian Yangjiagou Formation in Eastern Changchun,China: Evidence from Clay Mineral Geothermobarometers

The metamorphic conditions of the Upper Permian Yangjiagou Formation in eastern Changchun, China, were evaluated based on the mineral assemblage, illite crystallinity, illite polytypism,the b dimension of illite, and the chemical composition of chlorite. The pelitic rocks in the Yangjiagou Formation are characterized by illite + kaolinite + chlorite ± mixed-layer chlorite/smectite and detrital quartz + plagioclase. Illite in the formation has a crystallinity of 0.38-0.55 and comprises mixed 2 M_1 and1 M_d polytypes, indicating a metamorphic temperature of 200℃. Based on the chemical composition of chlorite and the chlorite geothermometer, we estimated diagenetic to very low-grade metamorphic conditions with temperatures of 185℃～204℃. The b dimension of illite varies from 8.992 A to 9.005 A.We used a mathematical algorithm to extend Guidotti and Sassi's(1986) diagram relating illite b dimension with temperature and pressure, and used this diagram, together with illite crystallinity and chlorite chemical composition, to semi-quantitatively estimate the formation pressure at1.2 kbar. These reveal that the Yangjiagou Formation has experienced very low-grade metamorphism.     

贵州新民铝土矿矿床Li的地球化学特征与富集机制探究

新民铝土矿床位于黔北务川-正安-道真地区(简称务正道地区)大塘向斜东翼,铝土矿(岩)型Li资源丰富.含矿岩系大竹园组(P1d)不同岩性的w(Li)有差别:土状-半土状铝土矿平均w(Li)为16.34×10-6,致密块状铝土矿平均w(Li)是803.84×10-6,铝土岩平均w(Li)是1436.22×10-6,黏土岩的平均w(Li)是786.62×10-6,梁山组泥岩的平均w(Li)是51.82×10-,韩家店群泥岩(页岩)的平均w(Li)是48.52×10-6,黄龙组灰岩的平均w(Li)是 11.99×10-6.由此可知,研究区铝土矿(岩)型Li资源主要富集在含矿岩系中上部的致密块状铝土矿、铝土岩和黏土岩中,顶板、底板以及土状-半土状铝土矿w(Li)较低.Li主要赋存于高岭石中,伊利石(水云母)和残存的三水铝石、勃姆石也可富集少量Li,当样品中赋锂矿物(高岭石、伊利石(水云母)、三水铝石和勃姆石)都存在时,高w(Li),主量元素w(Al3O2)、w(SiO2)、w(MgO)、w(K2O)、w(TiO2)和w(TFe2O3)与w(Li)的相关性也证实了上述结果.研究区的地球化学比值 CIA、w(Sr)/w(Cu)、u(CaO)/w(MgO)、w(Sr)/w(Ba)、w(V)/w(V+Ni)和 w(La)/w(Y)综合显示,炎热潮湿的古气候下,有机质腐烂形成酸性环境,半封闭海湾环境下,黏土化阶段中等强烈的化学风化程度和适宜的风化暴露剥蚀时间利于铝硅酸盐矿物和硅酸盐矿物化学键断裂,富集Al3+形成高岭石;风化程度过于强烈和长时间的风化剥蚀,继续脱Si富Al形成以硬水铝石为主的铝土矿;弱酸性-弱碱性以及氧化-还原过渡条件下,使得高岭石能最大程度的吸附Li元素.     

Occurrence of Li,B, Cu and Zn in some Egyptian Nile sediments

Lithium, boron, copper and zinc have been determined on cored and surface sediments from the delta and the drainage valley of the Nile River. The clay size fraction separated from the samples consists of montmorillonite and kaolinite as the predominant clay components, followed by illite and chlorite. Quartz and calcite are the non-clay admixtures.Lithium content varies between 7 and 48 ppm in the bulk sediments and between 28 and 61 ppm in the clay fractions, being clearly enriched in the clay material. In the clay fractions, concentration of lithium in kaolinite is indicated by a close relation between the lithium and kaolinite contents and is further supported by a close correlation with A1₂O₃.Boron in the clay fraction (62–112 ppm) appears to be concentrated in detrital illite.The concentrations of copper (26–900 ppm) and zinc (65–333 ppm) in the clay fractions correlate positively with the CO₂ percentage. Both elements tend to occur in or on the claysized grains of caleite.     

An integrated thermal and isotopic study of the diagenesis of the Brent group,Alwyn South,U.K. North Sea

The petrography, fluid inclusion thermometry and isotope geochemistry of diagenetic cements are used to reconstruct the pore-fluid history of the Middle Jurassic Brent Group reservoir sandstones in the Alwyn South area of the U.K. North Sea. The study focuses on a relatively limited area of three adjacent reservoir compartments at successively higher structural levels. The cement assemblage of kaolinite, quartz and illite has resulted in severe deterioration of otherwise good reservoir quality. Early precipitation of vermiform and late blocky kaolinite was succeeded by a period of relatively intense illite precipitation. Temperature estimates for kaolinite precipitation of 80°C andδ¹⁸O of ≈ + 15‰ (±3‰) suggest co-existing fluids ofδ¹⁸O ≈ −3‰. Quartz cementation overlapped both kaolinite and illite formation. Fluid inclusion data indicate that quartz cementation took place at temperatures of 109±7°C. Pore fluid salinities were ≈4 wt% NaCl with a H₂OO isotopic composition of ≈ -1 %o ± 0.5‰ SMOW. The fluids which precipitated coexisting illite were compositionally homogeneous with equilibriumδ¹⁸O water compositions of +0.5‰ SMOW. Illite SD values range from −33 to −50‰ SMOW. These fluid inclusion and isotopic data suggest that both quartz and illite were precipitated from pore waters with a uniform, marine signature. This is consistent with the predominantly marine to paralic depositional context of the Brent Group in Alywn South. Illite precipitation was followed by hydrocarbon emplacement between the Middle Eocene and Lower Oligocene.     

山西晋城和阳泉地区石炭系太原组铵伊利石矿物特征及成因

铵伊利石是伊利石层间域的K+被NH+4替代而形成的类质同象.文中运用X射线衍射分析、傅里叶红外光谱分析以及热重—热流—红外光谱同步分析等手段,对山西晋城及阳泉地区的15号煤层夹矸及煤中矿物进行了研究,发现15号煤层夹矸和煤低温灰中黏土矿物以铵伊利石和高岭石为主,铵伊利石含量为21％～74％;X射线衍射图谱上d(001)...     

Geochemical and mineralogical impacts of H2SO4 on clays between pH 5.0 and −3.0

Natural and constructed clay liners are routinely used to contain waste and wastewater. The impact of acidic solutions on the geochemistry and mineralogy of clays has been widely investigated in relation to acid mine drainage systems at pH > 1.0. The impact of H₂SO₄ leachate characterized by pH < 1.0 and potentially negative pH values on the geochemistry and mineralogy of clays is, however, not clear. Thus, laboratory batch experiments were conducted on three natural clay samples with different mass ratios of smectite, illite and kaolinite to investigate the impact of H₂SO₄ on the geochemistry and mineralogy of aluminosilicates from pH 5.0 to −3.0. Batch testing was conducted at seven pH treatments (5.0, 3.0, 1.0, 0.0, −1.0, −2.0 and −3.0) using standardized H₂SO₄ solutions for four exposure periods (14, 90, 180, and 365 d). Aqueous geochemical and XRD analyses showed: increased dissolution of aluminosilicates with decreasing pH and increasing exposure period, that smectite was more susceptible to dissolution than illite and kaolinite, precipitation of an amorphous silica phase occurred at pH ? 0.0, and anhydrite precipitated in Ca-rich clays at pH ? −1.0. In addition, global dissolution rates were calculated for the clays and showed good agreement to literature smectite, illite and kaolinite dissolution rates, which suggests global dissolution rates for complex clays could be determined from monomineralic studies. A stepwise conceptual model of the impact of H₂SO₄ on aluminosilicate geochemistry and mineralogy between pH 5.0 and −3.0 is proposed.