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1.
Daniel J. Casagrande Kristine Siefert Charles Berschinski Nell Sutton 《Geochimica et cosmochimica acta》1977,41(1):161-167
Six sulfur forms were investigated in profiles of freshwater- and marine-derived peat-forming systems of the Okefenokee Swamp, Georgia and Everglades Swamp, Florida. Total sulfur levels of 0.1–10% were found, thus indicating a major incorporation of sulfur in the very early stages of coal formation. The quantities of hydrogen sulfide and elemental sulfur observed appeared to be indicative of whether marine or freshwater conditions prevailed at the site of deposition. Carbon-bonded sulfur accounted for 70% of the total sulfur in the freshwater peat and 50% of the total sulfur in the marine peat. Over 15% of the total sulfur was in pyritic combination in the marine environment, while levels of pyrite in the freshwater peats were an order of magnitude lower. An ester-sulfate fraction represented 25% of the total sulfur in both freshwater and marine peats. The levels of sulfur forms in the peat profiles are compared to those observed in living plants and to various coals; levels of pyrite and organic sulfur in the peat are similar to those found by other investigators in freshwater-derived and marine-derived coals. 相似文献
2.
Hassan Baioumy 《Chemie der Erde / Geochemistry》2010,70(1):61-67
Jurassic high-sulfur coals from the Maghara area in Egypt were analyzed for the abundance and isotopic composition of different forms of sulfur. Analyses indicated that the sulfur occurs in the form of organic, pyrite, and sulfate forms. Pyrite sulfur represents the major fraction, while sulfate sulfur is minor and could be formed during sample preparation for the analyses.The δ34S CDT values of the organic sulfur are positive ranging between 1.0‰ and 13.5‰ with an average of 9.1‰. Pyrite δ34S values are also positive ranging between 1.5‰ and 15.4‰ with an average of 6.6‰. The high δ34S values of the organic sulfur in the Maghara coals suggest a freshwater origin of the organic components of these coals. The lack of correlation between pyrite and organic sulfur isotopes implies different incorporation mechanisms of sulfur. The high-sulfur contents along with the positive and high δ34S values suggest a marine origin of pyrite sulfur and support the geological interpretation of marine invasion after the peat formation that was responsible for the incorporation of the pyrite sulfur.The occurrence of pyrite as euhedral crystals as well as the high and positive δ34S values of the pyrite sulfur indicates the formation of pyrite during diagenesis as a result of marine water invasion of the preexisting peat in a brackish coastal plain environment. 相似文献
3.
沁水盆地晚古生代煤中硫的地球化学特征及其对有害微量元素富集的影响 总被引：1，自引：0，他引：1
煤中硫是多种有害微量元素的重要载体。基于形态硫分析、电感耦合等离子质谱及X射线衍射等方法分析沁水盆地晚古生代煤中硫和有害微量元素的分布规律,探讨了煤中硫对有害微量元素富集的影响,运用带能谱的扫描电镜和光学显微镜划分煤中硫化物的微观赋存特征。结果表明,沁水盆地煤中硫整体上以有机硫为主,平均占全硫的78%,只有在太原组个别高硫煤中以黄铁矿硫为占优势。显微镜和扫描电镜下可识别出煤中黄铁矿的微观赋存状态包括莓球状、薄膜状、晶粒状、结核状、团窝状黄铁矿和细粒黄铁矿集合体,白铁矿的微观赋存特征包括聚片状、板状和矛头状白铁矿,部分白铁矿与黄铁矿共生。沁水盆地煤中有害微量元素含量整体较低,黄铁矿是有害微量元素As、Se和Hg的重要载体,而有机硫决定了煤中U的富集。研究认为,成煤时期海水对泥炭沼泽的影响导致太原组煤中全硫和黄铁矿硫较高,太原组煤中硫的来源具有多样性,煤中黄铁矿具有多阶段演化的特点。 相似文献
4.
Distribution of forms of sulfur in peats from saline environments in the Florida Everglades 总被引：1，自引：0，他引：1
Although there is published information on the mechanism of sedimentary pyrite formation resulting from bacterial reduction of sulfate, little is known about the distribution of forms of sulfur, including organic, in peats. In order to increase understanding of the geochemistry of sulfur in coals, we have determined distributions of forms of sulfur in five cores of saline peat and one of brackish peat, all from areas near the Shark River and Whitewater Bay in the coastal swamps of south Florida. All concentrations vary widely with depth. Total sulfur concentrations range up to 6% of dry solids. Minor amounts of sulfur are present as H2S, S0, SO42−, and acid-soluble sulfide, but the principal forms are usually pyritic and organic. The ratio, organic/pyritic, is highly variable, but at a majority of levels in a profile is considerably greater than unity. It is inferred that topochemical factors are important in determining the distribution of sulfur forms in any element of volume. 相似文献
5.
J. Schieber 《Mineralium Deposita》1990,25(1):7-14
Extensive horizons of pyritic shale occur in Mid-Proterozoic sediments of the eastern Belt basin, Montana, U.S.A. These pyritic shales are of striped appearance. Laminated pyrite beds alternate with nonpyritic shale beds. Laminated pyrite beds have wavycrinkly internal laminae and are interpreted as mineralized microbial mats. Pyrite is essentially the only sulfide mineral in these shales. Pyritic shale horizons occur along the basin margins, and it is feasible that colloidal iron was introduced by rivers into basin marginal lagoons and then incorporated into microbial mats and reduced to pyrite. The pyritic shales in the Newland Formation show great similarity to those that host the Pb-Zn deposits of Mt. Isa and McArthur River. It is suggested that pyritic shales of this kind are relatively common in Mid-Proterozoic shales, and that the processes that led to the occasional formation of Pb-Zn ore bodies in these shales are not related to those that formed the pyritic shales themselves. 相似文献
6.
Pyrite is easily oxidized, and therefore unambiguous evidence of detrital pyrite grains in metasediments is a significant constraint on when an oxygenated atmosphere developed. Compact rounded pyrite in
7.
K. G. McQueen 《Mineralium Deposita》1989,24(2):100-110
Geochemically anomalous, pyritic sediments occur directly above a Mid Silurian unconformity in the Quidong area of southeastern New South Wales. The composition of these sediments reflects derivation from a mixture of: (a) feldspar- and mica-depleted detritus reworked from underlying quartz-rich flysch; (b) Mg-rich clay or chlorite precipitated from hydrothermal exhalations; and (c) pyrite formed by reaction of iron in clays or oxides with reduced sulphur derived largely from sea-water sulphate and possibly a magmatic source. Three types of base metal sulphide mineralisation occur at Quidong including: (a) weak syngenetic concentrations in the pyritic sediments; (b) stratabound and fault-controlled bodies of massive sulphides hosted by the pyritic sediments and containing higher grade Pb, Zn and Cu; and (c) small vein and cavity fillings of galena, barite and other minor sulphides in overlying limestones. All types of mineralisation are related to hydrothermal activity which occurred during and after deposition of the pyritic facies. The geochemistry of the immediately underlying basement rocks and Pb isotope data indicate that the source of the metal-bearing fluids was deeper in the crust and probably related to widespread partial melting and magmatic processes. The sulphidic sediments and stratabound sulphide deposits represent syngenetic-epigenetic, sediment hosted mineralisation developed in a shallow marine environment, distal from major volcanic centers. This style of mineralisation has not previously been described from the region. It has some similarities to the Irish-Alpine type spectrum of deposits best known in Europe. 相似文献
8.
Pyrite textures in five stratiform lead-zinc deposits from lower to upper greenschist facies environment of the Canadian Cordillera
are described and discussed in terms of deposition/early diagenesis, deformation, metamorphism and hydrothermal alteration
processes. Overgrowth is an important process during both diagenesis and deformation. Diagenetic and deformational overgrowths
can be distinguished. Diffusive mass transfer, involving pressure solution and oriented overgrowth of pyrite is the main deformation
mechanism in pyrite deposits at low metamorphic grades. Although diffusive mass transfer favours fine-grained mineral aggregates,
its effect on coarse pyrite grains has also been identified. Ore minerals dissolved by pressure solution may be transported,
with the assistance of pore fluids within fractures and grain boundaries, over distances significantly greater than the scale
of individual grains to give a range of pressure solution/overgrowth textures. The textural modification of pyritic ores from
the early stages of diagnesis, through metamorphism and deformation, to post deformation thermal annealing, has important
implications for the distribution of trace elements and isotopic compositions in pyritic ores. 相似文献
9.
10.
The sulfur isotopic composition of the Herrin (No. 6) Coal from several localities in the Illinois Basin was measured. The sediments immediately overlying these coal beds range from marine shales and limestones to non-marine shales. Organic sulfur, disseminated pyrite, and massive pyrite were extracted from hand samples taken in vertical sections.The values from low-sulfur coals (< 0.8% organic sulfur) underlying nonmarine shale were +3.4 to +7.3%0 for organic sulfur, +1.8 to +16.8%0 for massive pyrite, and +3.9 to +23.8%0 for disseminated pyrite. In contrast, the (> 0.8% organic sulfur) underlying marine sediments were more variable: organic sulfur, ?7.7 to +0.5%0, pyrites, ?17.8 to +28.5%0. In both types of coal, organic sulfur is typically enriched in 34S relative to pyritic sulfur.In general, δ 34S values increased from the top to the base of the bed. Vertical and lateral variations in δ 34S are small for organic sulfur but are large for pyritic sulfur. The sulfur content is relatively constant throughout the bed, with organic sulfur content greater than disseminated pyrite content. The results indicate that most of the organic sulfur in high-sulfur coals is derived from post-depositional reactions with a 34S-depleted source. This source is probably related to bacterial reduction of dissolved sulfate in Carboniferous seawater during a marine transgression after peat deposition. The data suggest that sulfate reduction occurred in an open system initially, and then continued in a closed system as sea water penetrated the bed.Organic sulfur in the low-sulfur coals appears to reflect the original plant sulfur, although diagenetic changes in content and isotopic composition of this fraction cannot be ruled out. The wide variability of the δ 34S in pyrite fractions suggests a complex origin involving varying extents of microbial H2S production from sulfate reservoirs of different isotopic compositions. The precipitation of pyrite may have begun soon after deposition and continued throughout the coalification process. 相似文献
11.
The stable enrichment of pyrite from magnesite ores in δ34S isotope (from 5.4 to 6.9‰) compared with pyrite from the host (sedimentary and igneous) rocks was established in the classical Satka sparry magnesite ore field. Concretionary segregations of fine-grained pyrite in dolomite are depleted in the heavy sulfur isotope (δ34S, from–9.1 to–5.8‰). Pyrite from dolerite is characterized by δ34S values (–1.1 and 1.7‰) close to the meteorite sulfur. The δ34S values in barite from the underlying dolomite horizon vary in the range of 32.3–41.4‰. The high degree of homogeneity of the sulfur isotope composition in pyrite from magnesite is a result of thermochemical sulfate reduction during the syngenetic crystallization of pyrite and magnesite from epigenetic brines, formed during dissolution of evaporite sulfate minerals at the stage of early catagenesis of the Riphean deposits.
相似文献12.
Pyrite: physical and chemical textures 总被引：9，自引：0，他引：9
Pyrite may crystallize initially in forms as diverse as framboids or cubes depending upon the temperatures and pressures.
Fluid-rich diagenesis or low-grade metamorphism clearly results in thorough recrystallization and the common formation of
cubes. Once these have formed, the pyrite becomes much more refractory and retains many characteristics even in deposits which
have undergone penetrative deformation. This is in strong contrast to the behavior of most of the accompanying sulfides, which
often undergo ductile deformation, solid state or chemical remobilization, and annealing. Pyrite deforms sparingly until there
is brittle failure; however, there may be significant pyrite corrosion and regrowth during metamorphism as the result of sulfur
exchange with other minerals, especially pyrrhotite. Pyrite fabrics may also be significantly modified by pressure solution
or Coble creep. Optical microscopic examination and electron microprobe chemical mapping of pyrites from a variety of mineral
deposits, including several high-grade metamorphic ones, reveals that the pyrites frequently contain both physical and chemical
textures that may be interpreted in terms of the depositional and the post-depositional history of the deposits. Inclusions
of sulfides or other minerals reveal information on the timing of the crystallization or recrystallization of the pyrite;
chemical mapping of elements such as Ni, Co, and As reveals information on the relative time of transport of these elements
in the ore fluids.
Received: 19 March 1997 / Accepted: 14 May 1998 相似文献
13.
Macroscopic pyrite crystals originating from a variety of geologic settings were made into thick sections. Electrical properties were measured with a Hall system, and minor element composition was analyzed with laser ablation inductively coupled plasma mass spectroscopy (LA-ICPMS). Selected thick sections were oxidized in a moist air environment inside a glove chamber. The relative metal content of surface products formed during oxidation was analyzed by LA-ICP-MS. Natural pyrite exhibits a range of electrical properties corresponding to the content of the common minor elements Co, As and Ni. These properties are similar to those of synthetic pyrite doped with single elements. Pyrite enriched in Co is an n-type semiconductor with low resistivity and high carrier mobility, while arsenian pyrite tends to be p-type and have higher resistivity. The effect of Ni is weaker and tends to be obscured by Co and As in samples of mixed composition. Cobalt demonstrates the strongest effect on electrical properties. Enrichment of Co at oxidized pyrite surfaces is inversely correlated with its concentration in the underlying pyrite. Cobalt enrichment in oxidation products is also more pronounced along crystal defects such as fractures, and in crystals with heterogeneous distribution of trace elements. These observations might be explained by differences in the electronic structure of pyrite arising from the presence of impurities, and by the distribution of domains with different impurity compositions, facilitating electron transfer. 相似文献
14.
硫是化学工业最重要的基本原料之一,主要用于生产化肥。我国硫矿资源工业开发利用的主要为硫铁矿和伴生硫。2007-2013年,中国地质调查局实施了全国化工矿产资源潜力评价项目,完成了全国硫矿成矿规律及预测研究,编制了相关图件,建设了数据库,取得了阶段性的成果。文章在以往研究和省级硫矿资源潜力评价成果的基础上,总结了全国硫矿时空分布特征,划分了成矿区带和成矿类型,建立了典型矿床和预测工作区的预测模型,最后对全国硫矿资源潜力进行了分类评价汇总。结果表明,全国共有硫矿床、矿点、矿化点共1 437处,其中硫铁矿1 418处,自然硫矿19处。成矿时代跨度为太古宙晚期-新生代,以元古宙硫矿储量最大。全国共划分为46个Ⅲ级硫矿成矿区带和17个矿集区;划分了沉积变质型、沉积型（海相、煤系）、岩浆热液型、海相火山岩型、陆相火山岩型、自然硫型6种预测类型和17个矿床式;梳理了6种预测类型典型硫矿床的预测要素和预测模型。全国共划分沉积变质型硫铁矿预测工作区20个,沉积型硫铁矿58个,岩浆热液型68个,海相火山岩型12个,陆相火山岩型9个,自然硫矿5个。全国共圈定硫矿3级预测区274个,其中硫铁矿268个,自然硫矿6个。全国硫铁矿硫铁矿和自然硫资源总量分别为241.35亿t和5.67亿t,其中预测资源量分别为184.57亿t和2.32亿t。根据成矿地质条件、矿床地质特征、矿石选冶性能、资源量可靠程度,文中遴选出21个硫矿优先勘查区,预测自然硫资源量2 229.3万t(S),硫铁矿50.58亿t(矿石)。该区成矿地质条件好,找矿潜力大,有一定的工作基础,已知矿床深边部等近期可优先安排勘查工作的预测区,远景好时可作为整装勘查基地。 相似文献
15.
V. L. Tauson R. G. Kravtsova V. I. Grebenshchikova E. E. Lustenberg S. V. Lipko 《Geochemistry International》2009,47(3):231-243
Pyrite crystals from gold deposits of various genetic types (mesothermal and epithermal) were examined by techniques of x-ray photoelectron and Auger electron microscopy and by scanning probe microscopy. The results confirm a conclusion made in earlier hydrothermal experiments that nonautonomous phases (NP) of variable composition occur on the surface of pyrite crystals. These phases are localized within a layer of submicrometer (nanometer) thickness (up to ～0.5 μm) within which the typochemistry of pyrite surface is pronounced. The development of sulfate on the surface of pyrite crystals from epithermal Au-Ag deposits is a typochemical feature of the origin of their ore mineralization at low temperatures and shallow depths. Supergene conditions are characterized by the presence of an oxi-hydroxide or oxide film of FeIII, which morphologically differs from the layer of a pyrite-like NP. The composition and properties of the NPs are different for pyrite from mesothermal and epithermal deposits: they are close to those of a pyrrhotite-like NP discovered on synthetic hydrothermal pyrite and contain an additional sulfite anion for pyrite from the former type of deposits and are close to sulfide-disulfide ensembles with trivalent Fe for pyrite from the latter type of deposits. Trace elements, including precious metals, can be accommodated in such a phase via the stabilization of clusters with Fe3+ and SO 4 2? in its structure. The instability of the crystallization process in epithermal environments may bring about the development of double-level nanostructure because of the structural transformation of vicinal surfaces into a set of ordered domains and the synthesis of nonautonomous “precursor” phases. Such systems can be stabilized via the excess dissolution of admixtures or the transition of the surface layer into another phase state. 相似文献
16.
On the Recent lobe of the Fraser River delta peat accumulation has actively occurred on the distal lower dilta plain, the transition between upper and lower delta plains, and the alluvial plain.Distal lower delta plain peats developed from widespread salt and brackish marshes and were not influenced appreciably by fluvial activity. Lateral development of the marsh facies were controlled by compaction and eustatic sea level rise. The resulting thin, discontinuous peat network contains numerous silty clay partings and high concentrations of sulphur. Freshwater marsh facies formed but were later in part eroded and altered by transgressing marine waters. The peats overlie a thin, fluvial, fining-upward sequence which in turn overlies a thick, coarsening-upward, prodelta—delta front succession.Lower delta plain—upper delta plain peats initially developed from interdistributary brackish marshes and were later fluvially influenced as the delta prograded. The thickest peats occur in areas where distributary channels were abandoned earliest. Sphagnum biofacies replace sedge-grass-dominated communities except along active channel margins, where the sedge-grass facies is intercalated with overbank and splay deposits. The peats are underlain by a relatively thin sequence of fluvial deposits which in turn is underlain by a major coarsening-upward delta front and pro-delta sequence.Alluvial plain peats accumulated in back swamp environments of the flood plain. Earliest sedge-clay and gyttjae peats developed over thin fining-upward fluvial cycles or are interlaminated with fine-grained flood deposits. Thickest accumulations occur where peat fills small avulsed flood channels. Overlying sedge-grass and Sphagnum biofacies are horizontally stratified and commonly have sharp boundaries with fine-grained flood sediments. At active channel margins however, sedge-grass peats are intercalated with natural levee deposits consisting of silty clay. These levees reduce both the number and size of crevasse splay deposits.Coal originating from peats of the different environments of the Fraser delta would vary markedly in character. Peats of the lower delta plain will form thin lenticular coal seams with numerous splits and have a high ash and sulphur content. Peats from the lower to upper delta plain will be laterally extensive and of variable thickness and quality. Basal portions of the seams will contain numerous splits and have a high sulphur content whereas upper portions will be of higher quality. Peats from the upper delta plain—alluvial plain will form thick, isolated and laterally restricted coal seams characterized by low ash and sulphur contents. 相似文献
17.
V. L. Tauson R. G. Kravtsova V. V. Akimov S. V. Lipko A. M. Spiridonov A. E. Budyak I. Yu. Voronova O. Yu. Belozerova K. Yu. Arsentev 《Doklady Earth Sciences》2018,478(1):92-99
Pyrite crystals and ore-bearing shales of the Degdekan deposit were studied by means of XPS, SEM–EDX, EPMA, and AAS. Five peaks of carbon organic forms were identified, conforming to polymer compounds containing either double bonds of carbon or alkyne groups and compounds containing C–OH and C=O bonds, as well as, probably, small amounts of S-containing compounds and those with functional groups of carboxylic acids. Sulfate prevails over sulfite in pyrites; among the surface sulfide forms, disulfide prevails over monosulfide; the presence of polysulfide is registered. The occurrence of various chemical forms of sulfur on the surface might provide for concentrating of microelements including the noble metals (NMs) in their surface-bound forms. The regular behavior of NMs (Au, Pt, Pd, and Ru) depending on the grain sizes (specific surfaces) of pyrite crystals along with the narrow range of the ratios of structural and surface components of the concentrations of different NMs points to NM coprecipitation with pyrite during the same productive stage. No capture of NM-containing carbonaceous phases took place, which should violate the regularity of Au distribution in pyrites of the Sukhoi Log deposit. 相似文献
18.
沉积过程对自生黄铁矿硫同位素的约束 总被引：6，自引：3，他引：3
自生黄铁矿是海洋沉积物中还原态硫的主要赋存形式,其形成过程与有机质矿化相关,影响全球的C-S-Fe生物地球化学循环。自生黄铁矿硫同位素分馏主要受微生物硫酸盐还原的控制,但近期的研究成果表明局部沉积环境的改变也可以影响黄铁矿硫同位素的组成,特别是在浅海环境。在浅海非稳态沉积环境内,物理再改造和生物扰动作用,导致硫酸盐还原带内生成的硫化物被再氧化,进而影响黄铁矿的硫同位素值。浅海沉积过程容易受到古气候和海平面变化的影响,引起沉积速率的剧烈波动,导致有机质和活性铁输入的不稳定,进而影响成岩系统的开放性和硫酸盐还原速率,最终影响黄铁矿的硫同位素值。另外,沉积速率的改变还影响硫酸盐—甲烷转换带的迁移,造成有机质和甲烷厌氧氧化硫酸盐还原的相互转化,产生不同的硫同位素信号。东海内陆架泥质区为研究沉积过程对自生黄铁矿的形成及其硫同位素组成的约束机制提供了很好的研究材料。该区域有很好的沉积学研究基础,自生黄铁矿丰富、并且个别层位有生物气（甲烷为主）存在,是研究边缘海C-S-Fe循环的理想场所。 相似文献
19.
广西宁明组植物化石中黄铁矿及其沉积意义 总被引：1，自引：1，他引：0
对化石中的黄铁矿进行研究,有助于明确生物的化石化过程以及期间的沉积微环境。利用光学显微镜和扫描电镜,对广西宁明组植物化石中保存的黄铁矿进行了分析,发现离散型单晶和成群的莓状体共同保存。单晶绝大多数为无规则至球状体,晶棱不明显,表面可见凹点;少数为八面体,晶棱明显,表面光滑;单晶直径为0.79~1.58 μm;莓状体为圆球状,粒径为7.23~14.95 μm,S/Fe原子个数比的均值为1.54。莓状体的粒径大小和变化幅度均处于低值段,其S/Fe原子个数比值小于2,结果均说明当时植物体上、下表皮间为一种贫氧的水体环境,并在短时间内形成了莓状体。植物化石上、下表皮间由于未保存组织结构,而被大量的、近似层状分布的黄铁矿单晶和莓状体充填,结果支持了化石内莓状体形成与有机质降解之间存在着必然联系。 相似文献
20.
《International Journal of Coal Geology》1988,9(4):371-383
This paper presents a statistical relationship between the pyrite particle size distribution and the potential amount of pyritic sulfur reduction achieved by specific-gravity-based separation. This relationship is obtained from data on 26 Ohio coal samples crushed to 14 × 28 mesh. In this paper a prediction equation is developed that considers the complete statistical distribution of all the pyrite particle sizes in the coal sample.Assuming that pyrite particles occurring in coal have a lognormal distribution, the information about the particle size distribution can be encapsulated in terms of two parameters only, the mean and the standard deviation of the logarithms of the grain diameters. When the pyritic sulfur reductions of the 26 coal samples are related to these two parameters, a very satisfactory regression equation (R2 = 0.91) results. This equation shows that information on both these parameters is needed for an accurate prediction of potential sulfur reduction, and that the mean and the standard deviation interact negatively insofar as their influence on pyritic sulfur reduction is concerned. 相似文献