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排序方式: 共有104条查询结果,搜索用时 205 毫秒
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海洋天然气水合物发育顶界的模拟计算 总被引:1,自引:1,他引:0
天然气水合物顶界的确定对于其资源评价十分重要,但目前还没有很好的方法来确定.本文利用在甲烷-硫酸根(SMI)界面硫酸根与甲烷所消耗的量相等和水-天然气水合物二相体系甲烷溶解度模型,建立了水合物顶界埋深计算的数学模型,并考虑硫酸根氧化有机质和微生物原位甲烷生成的影响.计算的ODP1245和IODP1327站位水合物顶界埋深分别为53 mbsf和83 mbsf,与钻探获得的水合物顶界埋深相吻合. 相似文献
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Precise hydrogeochemical modeling of early diagenesis is a key in the reconstruction of sedimentary basin models. This determines the mineralogical evolution of the sediment and consequently the porosity of the rock. During early diagenesis also part of the initial organic matter is converted into biogenic gas: CH4 CO2, and H2S. These processes are part of complex reaction chains during sedimentation, and biogeochemical reactions leave different signals that can be observed today. In this work, we reproduce the early diagenetic processes as integrated signals over geological times in sediments of the Demerara Rise by applying chemical thermodynamics using the PHREEQC (version 2) computer code. The investigated sediments are characterized by the presence of black shales in 410–490 mbsf and by a diagenetic barite layer above in 300–350 mbsf at depth of sulfate-methane transition (SMT). We determine the parameters that influence the location of diagenetic barite peaks in sediments overlying black shales by means of a novel modeling approach. Crucial parameters are the amount of bacterial organic matter mineralization, sedimentation rates and bottom water sulfate concentrations. All parameters are intertwining and influence the sulfate-methane cycle. They affect the location of the SMT visualized by diagenetic barite peaks. However, our model approach opens a wide field in exploring early diagenetic reactions, processes and products (such as biogenic methane) over geological times mirrored by diagenetic minerals and pore water concentration profiles that can be detected in present-day sediments. 相似文献
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Sulfide and iron control on mercury speciation in anoxic estuarine sediment slurries 总被引:2,自引:0,他引:2
Seunghee Han Anna Obraztsova Patrizia Pretto Dimitri D. Deheyn Joris Gieskes Bradley M. Tebo 《Marine Chemistry》2008,111(3-4):214-220
In order to understand the role of sulfate and Fe(III) reduction processes in the net production of monomethylmercury (MMHg), we amended anoxic sediment slurries collected from the Venice Lagoon, Italy, with inorganic Hg and either potential electron acceptors or metabolic byproducts of sulfate and Fe(III) reduction processes, gradually changing their concentrations. Addition of sulfide (final concentration: 0.2–6.3 mM) resulted in an exponential decrease in the sulfate reduction rate and MMHg concentration with increasing concentrations of sulfide. Based on this result, we argue that the concentration of dissolved sulfide is a critical factor controlling the sulfate reduction rate, and in turn, the net MMHg production at steady state. Addition of either Fe(II) (added concentration: 0–6.1 mM) or Fe(III) (added concentration: 0–3.5 mM) resulted in similar trends in the MMHg concentration, an increase with low levels of Fe additions and a subsequent decrease with high levels of Fe additions. The limited availability of dissolved Hg, associated with sulfide removal by precipitation of FeS, appears to inhibit the net MMHg production in high levels of Fe additions. There was a noticeable reduction in the net MMHg production in Fe(III)-amended slurries as compared to Fe(II)-amended ones, which could be caused by a decrease in the sulfate reduction rate. This agrees with the results of Hg methylation assays using the enrichment cultures of anaerobic bacteria: whereas the enrichment cultures of sulfate reducers showed significant production of MMHg (4.6% of amended Hg), those of Fe(III), Mn(IV), and nitrate reducers showed no production of MMHg. It appears that enhanced Fe(III)-reduction activities suppress the formation of MMHg in high sulfate estuarine sediments. 相似文献
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锂云母、铯榴石等矿物的硫酸盐焙烧浸出,是从中提取锂铷铯钾等碱金属元素的重要步骤,所得硫酸盐浸出液可近似看作Li+,Na+,K+,Rb+,Cs+ // SO42--H2O六元水盐体系;其在浓缩过程呈现复杂的成盐特征,增加了各碱金属元素分离提取的难度,研究其相关水盐体系相图和相平衡性质对理解浸出液中碱金属的分离具有重要的理论指导意义。本文采用Pitzer-Simonson-Clegg超额Gibbs自由能方程和具有内在热力学一致性的CALPHAD方法,构建了Na+,K+,Rb+,Cs+//SO42--H2O五元体系的多温固液相平衡热力学模型。借助该模型:1)实现了对Na2SO4+Rb2SO4+H2O、Na2SO4+Cs2SO4+H2O和K2SO4+Cs2SO4+H2O三元体系的多温溶解度等温线的准确描述,并进一步构建了这些体系在240.15~380.15 K温度范围内的多温相图;2)实现了对K2SO4+Rb2SO4+H2O和Rb2SO4+Cs2SO4+H2O体系中存在的固溶体相—水溶液平衡关系的准确描述,确认了(K,Rb)2SO4连续固溶体、以及(Rb,Cs)2SO4(α)和(Rb,Cs)2SO4(β)间断固溶体存在的合理性;3)预测了上述五元体系中所包含的全部4个四元子体系(Na2SO4+ K2SO4+ Rb2SO4+H2O、Na2SO4 + K2SO4+Cs2SO4+ H2O、Na2SO4+ Rb2SO4+Cs2SO4 + H2O和K2SO4+Rb2SO4+Cs2SO4+ H2O)的相图,明确了四元相图中固溶体的类型及形成区域。然而,模型预测结果与现有四元体系实验数据间存在普遍的不一致性,尤其是固溶体形成区域,但模型预测结果从非实验角度给出了重要参考,对现有实验提出了挑战,未来对这些体系开展更为精细的实验研究非常必要。 相似文献
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安徽庐江泥河铁矿矿床地球化学特征及其对成因的制约 总被引:6,自引:2,他引:4
泥河铁矿位于长江中下游成矿带庐枞中生代火山岩盆地中,矿床具有典型玢岩型铁矿的地质特征,是研究玢岩型铁矿成因的良好对象。本次工作在详细的野外观察及室内研究的基础上,对泥河铁矿主成矿期矿石矿物的稀土元素、硫同位素及铅同位素进行了分析测试工作。主成矿期磁铁矿、黄铁矿稀土元素配分模式呈现LREE富集、HREE曲线平直、Eu轻微负异常的特征,与赋矿砖桥组熔岩、闪长玢岩的稀土元素配分模式较为一致,结合矿石矿物与围岩的铅同位素特征,推测成矿金属元素主要来源于赋矿的火山-次火山岩,可能有少量壳源物质的加入。黄铁矿与硬石膏的硫同位素表现出双峰式分布的特征,说明岩浆活动与三叠纪膏盐层均对硫有所贡献。三叠纪膏盐层在泥河铁矿的成矿过程中,不仅仅是重要的矿化剂,同样是铁质沉淀的氧化剂。综合矿床地质与地球化学特征,认为泥河铁矿是由次火山岩体演化产生的含矿高温热液在闪长玢岩穹窿顶部,通过交代充填作用形成的玢岩型铁硫矿床。 相似文献
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Microbial signatures in sabkha evaporite deposits of Chott el Gharsa (Tunisia) and their astrobiological implications 总被引:1,自引:0,他引:1
This study investigates the geomicrobiological potential of Upper Pleistocene evaporite deposits of the Chott el Gharsa, a wide continental sabkha in southern Tunisia. Organic and inorganic-derived biosignatures are mostly contained in microcrystalline, laminated gypsum lithofacies consisting of light/dark alternations of concordant laminae, which have precipitated from high salt concentrated waters. These biosignatures include mineralized microbial-interpreted morphologies, such as mucilage, rods, and microfibers, and dumbbell morphologies in the hollow cores of dolomite crystals that are associated with sulfates. Mineral products that are induced by microbial activity and their organic compounds lead to the formation of lenticular-shaped gypsum crystals, with a high length/width ratio, dolomite precipitation and formation of pyrite framboids. Morphological and structural aspects of these biosignatures, and their composition, in laminated, dolomite-rich sulfate deposits could be detected through microscopic investigations and micro-analyses performed by the instrumentation that is planned for ongoing Mars sample return missions. 相似文献
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