Geochemistry of high-temperature coal ashes and the sedimentary environment of the New South Wales coals, Australia

Chemical analyses of high-temperature coal ashes were used to establish the distribution, association and relationship between major inorganic elements such as Si, Al, Ti, Fe, Mn, Mg, Ca, Na, K, P, S and CO₂ in a number of New South Wales economic coal seams and to study the composition and character of mineral matter in these coals. The methods used for the evaluation of the data were statistical analysis (univariate and bivariate), ratios, normative mineral composition and variation diagrams.The distribution of major and minor inorganic elements in coal appears to be related to the amount of mineral matter occurring in coal (determined as ash yield) and its mineralogical composition. The quantitative variations in levels of these elements can be classified as in-seam and inter-seam variations. In-seam variations are largely ash yield dependent, i.e. the levels of an element (wt.%) in coal increase along with the increase of its ash content (wt.%). The inter-seam variations are more complex and are related to both ash yield and to the mineralogical composition of mineral matter.The principal components of New South Wales coal ashes are silicon and aluminium. Silicon may be present as silica or combined with aluminium in different proportions to form clay minerals, such as kaolinite, illite, mixed-layer clay minerals, and smectite. Thus, the concentration levels of aluminium in relation to silicon in coal may give an indication about the character of clay minerals present in coal.Ratios and correlation coefficients of element pairs such as Al and Ti, Na and K, and Na and Al were used to determine differences in the chemical composition of high-temperature coal ashes of seams from various stratigraphic positions and provinces. In some seams the nature of associations of these elements is more significant than in others. This is interpreted as being a product of specific environmental conditions controlling the deposition of these seams.The nature of clay mineral content in coal is believed to be a major reason for chemical dissimilarities found between seams of various stratigraphic levels and geographic areas. For example, in some seams kaolinite, in others expandable clay minerals are dominant. The vertical distribution of these minerals has a stratigraphic significance. Within the Upper Permian Newcastle Coal Measures a trend from kaolinite-rich through to expandable minerals-rich and to kaolinite-rich assemblages can be observed from the bottom to the top. These changes are noticeably gradual.All significant variations in the clay mineral assemblages could relate to the long-term changes in the provenance of sedimentary material, weathering conditions in the source area and the rate of subsidence in the place of deposition. These changes are associated with major tectonic events controlling the history of sedimentation within the paralic Sydney and Gunnedah Basins during the Permian.     

风化型和含煤建沉积型高岭土的物质组成对比研究

我国高岭土资源丰富,矿床类型多,其中风化和含煤建造沉积型是两类比较重要的高岭土矿床,对这两类高岭土矿床化学组成,矿物组成及高岭石矿物学特征的异同点进行研究和探讨,其结果表明,风化高岭土的化学成分一般属硅高铝低型,钾含量偏高,钛含量低,铁含量则随成矿线岩和风化条件的不同波动范围大,矿物组成主要为结晶度较差的高岭石、水云线和石英,以及极少量的管状埃洛石,含煤建造沉积型高岭土一般属铝高硅低型,钾含量低,钛含量明显偏高,矿物组成简单,高岭石含量〉９５％,结晶度较好。     

Phase–mineral and chemical composition of composite samples from feed coals,bottom ashes and fly ashes at the Soma power station,Turkey

The phase–mineral and chemical composition of feed coals (FCs) and their bottom ashes (BAs) and fly ashes (FAs) produced in the Soma thermo-electric power station (TPS), Turkey, was characterized. FCs are high-ash Soma subbituminous coals abundant in moisture and Ca, and depleted in S. The inorganic composition (in decreasing order of significance) of FCs includes calcite, quartz, kaolinite, illite+muscovite, chlorite, plagioclase, gypsum, pyrite, montmorillonite, K-feldspar, dolomite, siderite, ankerite, opal, and volcanic glass. The results for 57 elements studied show that Ca>Nb>Cs>(V, Li) have significantly higher contents in FC ashes than the respective Clarke values for coal ashes. The water-soluble residues isolated from FCs include gypsum, calcite, inorganic amorphous matter, Ca–Mg–Na–K phase, and opal. These residues are enriched in Na>Se>S>B>Mg>Mo>Sr>Ca>K. The phase–mineral composition of BAs and FAs includes mainly glass, quartz, char, mullite, plagioclase, calcite, and portlandite; and, to a lesser extent, illite+muscovite, melilite, hematite, anhydrite, lime, cristobalite, kaolinite, and magnetite. Minor amounts of K-feldspar, dolomite, ankerite, Fe-spinel, gypsum, and Ca–K–Na phase also occur in BAs and FAs. FAs are enriched in inorganic matter, glass, cristobalite, mullite, Fe oxides, lime, and anhydrite, and depleted in mineral matter, char, quartz, clay minerals, melilite, portlandite, and carbonates in comparison with BAs. Only Se is significantly enriched in BAs and FAs compared to FC ashes. Most of the trace elements (in particular As, Bi, Cd, Ge, Pb, Sn, Tl, and W) are more abundant in FAs, while BAs are more enriched in Ca, Cs, Fe, Ho, Mn, P, Sc, Se and Tb. Significant percentages (11–59%) of elements initially present in FCs, namely S>Sb>Sn>Ta>Mo>Bi>Zn>Ni>Na>(Lu, Tm)>B, were emitted by stack emissions and not captured by the cleaning equipment in the Soma TPS. Some genetic features, properties, possible environmental concerns, and potential utilization directions related to FCs, BAs, and FAs are also discussed.     

华北地区京西煤田侏罗纪煤层中伊利石矿物学特征及成因

为了探讨伊利石对煤化作用和沉积环境的指示作用，以华北地区京西煤田侏罗纪煤层夹矸为研究对象，采用X射线衍射方法（XRD）和X射线荧光方法（XRF）分别测定煤层夹矸的矿物组成和化学组成，研究夹矸中伊利石矿物学特征及成因。结果表明，京西煤田侏罗纪煤层夹矸主要由伊利石、绿泥石和石英组成，其中，伊利石质量分数平均为62.92%。将XRD数据和XRF数据进行对比分析，计算得到伊利石平均化学式为（K_0.37（NH₄）_0.03）Al₂（Si_3.60Al_0.40O₁₀）（OH）₂。京西煤田煤层夹矸中伊利石主要由高岭石转化而来，伊利石的NH₄+占层间阳离子的比例具有随沉积古盐度升高而逐渐升高的趋势，n（Si）/n（Al）Ⅳ具有随煤化程度升高而逐渐降低的趋势，这表明京西煤田侏罗纪煤层夹矸中的伊利石矿物学特征对沉积环境和煤化作用具有一定的指示作用。      

The role of sulphide and carbonate minerals in the concentration of chalcophile elements in the bituminous coal seams of a paralic series (Upper Carboniferous) in the Upper Silesian Coal Basin (USCB), Poland

Sulphide and carbonate minerals from nine bituminous coal seams of a Paralic Series were investigated by means of polished-section microscopy, scanning electron microscopy and absorption spectral analyses. In addition to syngenetic accumulations of kaolinite, illite and quartz, diagenetic veinlets of subhedral pyrite and marcasite most often occur in vitrinite clast fissures and in post-tectonic fissures, nests and lenses with fusinite. Epigenetic anhedral and subhedral grains of ankerite, dolomite, siderite and calcite are also frequently found in post-tectonic veins. Pyrite replaced some of the marcasite grains and it dominates in older coal seams in the Flora Beds as compared with the Grodziec Beds. Occasionally there are anhedral and subhedral galena, sphalerite and chalcopyrite grains among coal macerals as well as cerussite among post-tectonic carbonate veins. They all represent the only minerals that are abundant in definite chalcophile elements (Cd, Co, Cu, Ni, Pb, Zn). In addition to the minerals just mentioned, the elements occurred in pyrite and ankerite grains, which contained inclusions of fusinite and other minerals (among others, clay and carbonate minerals in pyrite, pyrite in carbonates). Although there is a low content of minerals accumulating Cd, Co, Cu, Ni, Pb and Zn, the minerals significantly influence the average concentration of elements in the coal seams. In the Grodziec Beds, mineral matter, especially carbonates and sulphides, determines (>50%) the concentration of Cd, Cu, Pb and Zn in coal. The basic part of Cd, Co and Ni in the coal seams of the Grodziec Beds and of Co, Cu, Ni, Pb and Zn in coal seams of the Flora Beds originates from organic matter. These regularities can be important, from an ecological perspective, in stating whether the coals investigated are useful for combustion and in chemical processing.     

Geology and characterisation of the Pecket coal deposit, Magellan Region, Chile

The geology, petrography and chemical variation of the Pecket coal sequence, Magellan Region (52°57′S, 71°10′W), the only Chilean coal used for electricity generation on a large scale, has been studied in order to predict their combustion behaviour, especially in coal blends. The depositional environment of formation of the coal seams was a swamp rarely exposed to subaerial conditions and was associated with the development of the folded foreland of the Magellan basin during the Tertiary (Oligo–Miocene). The general tectonic regime of the collision of the Antarctic and South American plates is reflected by a system of joints with 40°N–50°W strike. The maceral composition of all six seams studied indicates high contents of vitrinite (>90%), minor content of liptinite (4.7%) and inertinite (<2%). Occurrence of tonstein horizons altered to kaolinite indicates a distal volcanism during peat accumulation. Coal rank varies between lignite and subbituminous (Ro=0.28–0.42%) with an average dry basis calorific value of 5450 kcal/kg, 17 wt.% moisture, 41 wt.% volatile matter, and sulphur content below 0.5 wt.%. The mineral matter (LTA) associated with the coal shows a dominance of kaolinite with quartz, smectite, and minor basanite. SiO₂/Al₂O₃ and Fe₂O₃/CaO ratios of the ashes diminish towards the lower seams. With respect to the utilisation of Pecket coals in combustion, base/acid ratios (B/A) and silica ratios (SR) indicate potential fouling for seams 1, 2, 5, and 6i, with high fouling indexes (Rf) for seams 2 and 5. Pecket coal is excellent for blend combustion due to its low sulphur content.     

西南喀斯特地区不同石漠化阶段土壤黏土矿物组成及其含量变异研究

为了探索西南喀斯特地区土壤中黏土矿物组成及其含量的变异规律,以贵州省普定县和荔波县不同石漠化阶段典型土壤的黏土矿物为例,采用x-射线衍射仪图谱分析方法,计算得到黏土矿物组成及其含量,探讨不同石漠化阶段黏土矿物组成变化规律及其含量之间的线性关系。结果表明：不同石漠化阶段黏土矿物的组成是相同的,均为高岭石、蒙脱石和伊利石;在未石漠化、轻度石漠化、中度石漠化阶段,蒙脱石在剖面表层的质量分数分别为27．82％、29．34％、58．32％,高岭石分别为21．39％、31．81％、36．93％,伊利石分别为50．79％、38．85％、4．75％;在西南喀斯特地区,各石漠化阶段伊利石与蒙脱石的含量之间以及伊利石和高岭石的含量之间都呈显著的线性相关,相关系数分别为-0．9703、-0．9456;西南喀斯特地区土壤相似的成土作用和成土环境造成了黏土矿物相同的组成,而黏土矿物含量的差异说明各成土作用的程度或阶段是不同的;粉粒中的黏土矿物主要为石英和白云母,而砂砾中的黏土矿物主要为石英。     

滇东黔西晚二叠世含煤沉积中火山灰蚀变形成的伊利石粘土岩夹矸

本文对广泛分布于滇东-黔西晚二叠世含煤沉积中粘土岩夹矸的岩石学、矿物学、化学组成和微量元素进行了研究。发现粘土岩夹矸的变种伊利石粘土岩夹矸(Illite-tonstein)在沉积盆地空间上成片分布,且与晚期成岩作用有明显的成因联系。粘土岩夹矸中粘土矿物构成与煤阶大体对应的关系,揭示了同沉积火山凝灰蚀变产物的后期变化趋势和规律。     

广西合浦新屋面高岭石矿物学特征及其形成途径

在野外实地考察的基础上,结合X射线衍射、扫描电镜(SEM)、化学成分分析等测试技术,对广西合浦新屋面高岭土矿床的风化物进行了研究。X射线衍射分析表明,黏土矿物主要为高岭石、伊利石、石英、正长石及斜长石。高岭石结晶度在0.489～1.210之间,随着深度的逐渐减小,高岭石逐渐增多,长石逐渐减少,高岭石的结晶程度则呈现变好的趋势,反映出花岗岩中原生矿物高岭土化程度逐渐加强。SEM结果表明,随着风化程度的加强,高岭石发育越来越好,晶形越来越完整。化学成分分析显示w(Al2O3)和w(K2O)互为消长关系,且随着深度的增大,Al2O3逐渐减少,K2O逐渐增多。该区长石蚀变为高岭土,可以经由绢云母中间阶段再转变形成高岭石和直接转变形成高岭石这两个途径。     

Metamorphism of mineral matter in coal from the Bukit Asam deposit, south Sumatra, Indonesia

The coal of the Miocene Bukit Asam deposit in south Sumatra is mostly sub-bituminous in rank, consistent with regional trends due to burial processes. However, effects associated with Plio–Pleistocene igneous intrusions have produced coal with vitrinite reflectance up to at least 4.17% (anthracite) in different parts of the deposit. The un-metamorphosed to slightly metamorphosed coals, with Rv_max values of 0.45–0.65%, contain a mineral assemblage made up almost entirely of well-ordered kaolinite and quartz. The more strongly heat-affected coals, with Rv_max values of more than 1.0%, are dominated by irregularly and regularly interstratified illite/smectite, poorly crystallized kaolinite and paragonite (Na mica), with chlorite in some of the anthracite materials. Kaolinite is abundant in the partings of the lower-rank coals, but is absent from the partings in the higher-rank areas, even at similar horizons in the same coal seam. Regularly interstratified illite/smectite, which is totally absent from the partings in the lower-rank coals, dominates the mineralogy in the partings associated with the higher-rank coal beds. A number of reactions involving the alteration of silicate minerals appear to have occurred in both the coal and the associated non-coal lithologies during the thermal metamorphism generated by the intrusions. The most prominent involve the disappearance of kaolinite, the appearance of irregularly interstratified illite/smectite, and the formation of regular I/S, paragonite and chlorite. Although regular I/S is identified in all of the non-coal partings associated with the higher-rank coals, illite/smectite with an ordered structure is only recognised in the coal samples collected from near the bases of the seams. The I/S in the coal samples adjacent to the floor of the highest rank seam also appears to have a greater proportion of illitic components. The availability of sodium and other non-mineral inorganic elements in the original coal to interact with the kaolinite, under different thermal and geochemical conditions, appears to be the significant factor in the formation of these new minerals, and distinguishes the mineralogical changes at Bukit Asam from those developed more generally with rank increases due to burial, and from the effects of intrusions into coals that were already at higher rank levels.     

Mineralogy and chemical composition of the clay fraction of Neogene shales from the Surma Group in the Bengal basin,Bangladesh

Mineralogical and chemical investigations (<2μm clay separates) of shale samples from the Neogene-age Surma Group obtained from four wells (Habiganj-11, Shahbazpur-1, Titas-11, Titas-15) in the Bengal basin, Bangladesh, were carried out in order to reveal the clay mineral composition as reservoir exploration and exploitation requires a good understanding of the clay minerals. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-Ray fluorescence spectrometry (XRF). Mineralogically, the sub-surface Surma Group shales comprise predominantly quartz, plagioclase, illite, chlorite, kaolinite, with lesser amounts of K-feldspar, dolomite and smectite, and minor to trace amounts of calcite, siderite and pyrite. The chemical composition of the <2 μm clay separates also suggests an illite and chlorite-rich composition. With increasing burial depth, the Surma Group shales are enriched in illite. The gradual decreasing of the smectite clays with depth and ultimate disappearance at greater depths (≥ 3000 m) may have been responsible for the presence of the diagenetic illite. Based on the mineralogical composition it is most likely that the illite-chlorite associations together with quartz and feldspar were predominantly detrital in origin and thus reflect the presence of a rapidly-rising source terrain not subjected to intense weathering.     

Geochemical characteristics of the coal gangues from the Du’erping coal mine,Xishan coalfield,North China

Inductively coupled plasma mass spectrometry, inductively coupled plasma optical emission spectroscopy, hydride generation-atomic fluorescence spectrometry, emission spectrometry, X fluorescence spectrometry, and X-ray diffraction were employed to study the geochemistry and mineralogy of coal gangues from Nos. 2, 3, and 8 coal seams of the Du’erping coal mine, Xishan coalfield, Taiyuan, Shanxi Province. The study revealed that compared with the sedimentary cover, upper continent crust, Carboniferous-Permian coal from North China, as well as most coal in China, coal gangues from Nos. 2 and 3 coal seams are rich in Li, Be, Sc, Cr, Cu, Ga, Ba, Th, Nb, Cd, Pb, Ta and rare-earth elements, and coal gangues from No. 8 coal seam are rich in Li, Sc, V, Cr, Ga, U, and rare-earth elements. Compared with the Carboniferous-Permian coal from North China and most coal in China, coal gangues from Nos. 2, 3 and 8 seams are rich in Rb, V, Cs and Sr. Therefore, The Du’erping coal gangues in the Xishan coalfield are rich in most hazardous trace elements and rare-earth elements, wherein the contents of Ga and Li reach the industrial grade and have significance for industrial utilization. On the whole, coal gangues of the Shanxi Formation from the Permian are rich in more trace elements than those of the Carboniferous Taiyuan Formation. The distributions of REE show obviously dipping rightwards with negative Eu anomalies. The contents of rare-earth elements in the three seams are quite different. All of the above indicate that the source of the rare-earth elements is terrigenous debris. Minerals in No. 2 seam identified by X-ray diffraction mainly include quartz, kaolinite, in addition to calcite, pyrite, apatite, epidote, and epsomite. No. 3 seam mainly contains quartz, kaolinite, in addition to a small amount of sodium feldspar, calcium nitrate, iron ore, gypsum, and vivianite. No. 8 seam mainly contains kaolinite, dickite, quartz, illite, and a small amount of hematite and U. The correlations between major elements and trace elements in coal gangues of the Du’erping coal mine analyzed by using SPSS (Statistical Product and Service Solutions) indicate that the trace alkali elements and rare-earth elements occur mainly in such clay minerals as kaolinite.     

Depositional conditions of the coal-bearing Hirka Formation beneath Late Miocene explosive volcanic products in NW central Anatolia,Turkey

This work focuses on the relationship between the coal deposition and explosive volcanism of the Miocene basin, NW central Anatolia, Turkey. The coal-bearing Hirka Formation was deposited over the Galatian Andesitic Complex and/or massive lagoonal environments during the Miocene. The investigated lignite is a high ash (from 32 to 58%) and sulphur (from 1.43 to 3.03%) lignite which is petrographically characterised by a high humunite content. The mineral matter of the studied lignite samples is made up of mainly clay minerals (illite-smectite and kaolinite), plagioclase and quartz in Bolu coal field, clay minerals (illite-smectite, smectite and illite), quartz, calcite, plagioclase and gypsum in Seben coal field, quartz, K-feldspar, plagioclase and clay minerals (kaolinite and illite) in K?br?sc?k, and dolomite, quartz, clinoptilolite, opal CT and gypsum in Çaml?dere coal field. The differences in these four types of lignite with specific mineralogical patterns may be due to the explosive volcanic events and depositional conditions which changed from one coal field to the others. There is a zonation from SW to SE in the studied area for zeolites such as Opal CT+smectite-clinoptilolite-analcime-K-feldspar. Carbonate minerals are commonly calcite in Seben and K?br?sc?k coal fields. In Bolu, coal samples are devoid of calcite and dolomite. These analyses show that there is an increase in the amount of Mg and a decrease in the amount of Na from the northwestern part to the southern part in the study area.     

Selected elements in major minerals from bituminous coal as determined by INAA: implications for removing environmentally sensitive elements from coal

The four most abundant minerals generally found in Euramerican bituminous coals are quartz, kaolinite, illite and pyrite. These four minerals were isolated by density separation and handpicking from bituminous coal samples collected in the Ruhr Basin, Germany and the Appalachian basin, U.S.A. Trace-element concentrations of relatively pure ( 99⁺%) separates of major minerals from these coals were determined directly by using instrumental neutron activation analysis (INAA). As expected, quartz contributes little to the trace-element mass balance. Illite generally has higher trace-element concentrations than kaolinite, but, for the concentrates analyzed in this study, Hf, Ta, W, Th and U are in lower concentrations in illite than in kaolinite. Pyrite has higher concentrations of chalcophile elements (e.g., As and Se) and is considerably lower in lithophile elements as compared to kaolinite and illite. Our study provides a direct and sensitive method of determining trace-element relationships with minerals in coal.Mass-balance calculations suggest that the trace-element content of coal can be explained mainly by three major minerals: pyrite, kaolinite and illite. This conclusion indicates that the size and textural relationships of these major coal minerals may be a more important consideration as to whether coal cleaning can effectively remove the most environmentally sensitive trace elements in coal than what trace minerals are present.     

Enrichment of lithium in the claystone coal gangue from the Malan mine,Xishan Coalfield,Shanxi Province,Northern China

In China, the lack of Li resources is in stark contrast to a large amount of coal gangue produced by coal mining. To determine the distribution patterns and existing status of lithium (Li) elements in the coal gangue, the mineralogical and geochemical analysis were formed on samples of the roof, floor, and parting of No. 02, 2, 8, and 9 coal seams, being mined in Malan mine, Xishan coalfield, Shanxi Province. The results show that the lithium content in this study area is relatively enriched, the highest content is 499 μg/g in sample 02-G, and the average content is 109.8 μg/g, which is two times that of the world average value of claystone (45 μg/g). XRD analysis shows that the mineral composition of parting samples is mainly clay mineral kaolinite, while the coal seam roof and floor samples also include quartz and some iron-bearing minerals, such as pyrite and siderite. Likewise, possible lithium-rich mineral phases and possible lithium-rich factors were investigated in this paper. A comprehensive clay separation experiment and correlation analysis between lithium and major elements indicate that lithium is likely to exist in the clay mineral kaolinite in the study area. It is also found that the content of Li adsorbed by cryptocrystalline kaolinite is generally higher than that of crystalline kaolinite. According to the mechanism of Li⁺ adsorption in clay minerals, the higher lithium content of cryptocrystalline kaolinite is due to its larger specific surface area, which can adsorb more lithium on the surface.     

Mineral matter and trace elements in coals of the Gunnedah Basin, New South Wales, Australia

The concentrations of major and trace inorganic elements in a succession of Permian coals from the Gunnedah Basin, New South Wales, have been determined by X-ray fluorescence techniques applied to both whole-coal and high-temperature ash samples. The results have been evaluated in the light of quantitative data on the minerals in the same coals, determined from X-ray diffraction study of whole-coal samples using a Rietveld-based interpretation program ( ™), to determine relationships of the trace elements in the coals to the mineral species present. Comparison of the chemical composition of the coal ash interpreted from the quantitative mineralogical study to the actual ash composition determined by XRF analysis shows a high degree of consistency, confirming the validity of the XRD interpretations for the Gunnedah Basin materials. Quartz, illite and other minerals of detrital origin dominate the coals in the upper part of the sequence, whereas authigenic kaolinite is abundant in coals from the lower part of the Permian succession. These minerals are all reduced in abundance, however, and pyrite is a dominant constituent, in coals formed under marine influence at several stratigraphic levels. Calcite and dolomite occur as cleat and fracture infillings, mostly in seams near the top and bottom of the sequence. The potassium-bearing minerals in the detrital fraction are associated with significant concentrations of rubidium, and the authigenic kaolinite with relatively high proportions of titanium. Zirconium is also abundant, with associated P and Hf, in the Gunnedah Basin coal seams. Relationships exhibited by Ti, Zr, Nd and Y are consistent with derivation of the original sediment admixed with the seams from an acid volcanic source. Pyrite in the coals is associated with high concentrations of arsenic and minor proportions of thallium; no other element commonly associated with sulphides in coals, however, appears to occur in significant proportions with the pyrite in the sample suite. Small concentrations of Cl present in the coal are inversely related to the pyrite content, and appear to represent ion-exchange components associated with the organic matter. Strontium and barium are strongly associated with the cleat-filling carbonate minerals. Ge and Ga appear to be related to each other and to the coal's organic matter. Cr and V are also related to each other, as are Ce, La, Nd and Pr, but none of these show any relationship to the organic matter or a particular mineral component.     

Geochemical and Mineralogical Characteristics of Pleistocene Lignites and Associated Sediments of Marathousa Coal Field,Central Peloponnese,Greece

The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.     

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.     

乌兰图嘎超大型锗矿床含锗煤的矿物学

内蒙古乌兰图嘎锗矿是我国近年来发现的产在煤层中的超大型锗矿床,锗金属储量达1600 t。以乌兰图嘎超大型锗矿床的含锗煤为研究对象,利用X射线衍射(XRD)、带能谱的扫描电镜(SEM-EDX)和电子探针(EPMA)详细研究了乌兰图嘎含锗煤及其同时代的红旗煤矿无矿煤的矿物学特征。分析结果表明,乌兰图嘎含锗煤中的主要矿物包括石英、蒙脱石;次要矿物包括长石、高岭石、伊利石;另含少量三水铝石、角闪石、叶蜡石、石膏、绿泥石、锐钛矿、黄铁矿、方解石、白云石和草酸钙石;微量的锆石、闪锌矿、白钨矿、重晶石、黄铜矿、卤化物、磷酸盐以及含Pb、Bi、Cr、As和Sb矿物。未发现含锗矿物。推测含锗煤中的锗可能主要呈有机结合,而Ba、Zn、Ti、W、Pb、Bi、Cr、Fe、As、Zr、Sb、Cu和REE可能主要与矿物相结合。此外,首次在乌兰图嘎含锗煤及红旗煤矿无矿煤中发现含银颗粒或自然银,推测胜利煤田的褐煤可能有相当规模的Ag矿化。     

钱塘江下切河谷SE2孔全新世沉积物黏土矿物特征及其意义*

通过X射线衍射系统分析了杭州湾地区SE2孔全新世沉积物的黏土矿物组成,结果显示研究层段黏土矿物主要由伊利石、绿泥石、高岭石和蒙脱石组成;伊利石结晶度较好,化学风化指数普遍大于0.5,表明以化学风化为主,且风化趋势自下而上呈递减趋势。通过对比中国东南部主要河流沉积物的黏土矿物组成,认为钱塘江下切河谷全新世沉积物的黏土矿物组成具有较好的物源指示意义: 全新世 Ⅰ 段(即古河口湾和河漫滩)沉积物主要来自钱塘江上游,特征黏土矿物为高岭石,河口外物质贡献不大;Ⅱ 段(即现代河口湾和近岸浅海)沉积物包含较多蒙脱石,表明不仅包括钱塘江上游物质,河口外长江物质也开始进入钱塘江河口。黏土矿物中,高岭石对气候有较好的指示作用:中全新世高岭石含量达到最高值,反映气候最为湿热,化学风化程度最高;晚全新世含量逐渐降低,反映气候逐渐回冷,化学风化强度降低。