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富钴结壳生长过程中铁锰氧化物 总被引：11，自引：0，他引：11
富钴结壳的矿物学研究是一个难点.本文运用电子探针微区分析结合X射线衍射和矿相显微镜观察的综合方法对富钴结壳中的铁锰氧化物矿物组合及其组分变化进行了研究.研究发现,富钴结壳是从与胶状粘土类混合共沉积开始生长的,结壳内部的韵律层和柱状构造也是始于粘土层终于粘土层的;铁锰团粒的核心一般是较纯的水羟锰矿小核心,可能是在生物媒介作用下在水体中形成后沉降叠积的.FM、FPE海山结壳的中层存在一较纯水羟锰矿层,但该层中Co含量FM15比FPE06低得多,可能反映了FM15在该层形成时Co通量较低.而该层在FN12中不存在,反映了区域环境的较大差异.在FN12火焰状构造亚带存在Mn氧化物和Fe氧化物的极度分异现象,可能反映了结壳形成环境的重大变化. 相似文献
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富钴结壳是继多金属结核资源之后被发现的又一深海沉积固体矿产资源,在太平洋、大西洋和印度洋的海底均有分布。据估算,全球三大洋海山富钴结壳干结壳资源量为(1081.1661~2162.3322)×108t。世界各国对富钴结壳的调查始于20世纪80年代初,截至目前,已有日本、中国、俄罗斯和巴西等4个国家与国际海底管理局签订了富钴结壳勘探合同,而韩国的矿区申请也于2016年获得核准。富钴结壳按形态可分为板状结壳,砾状结壳和钴结核3种类型。富钴结壳内部结构构造在宏观上通常表现为三层构造,即底部亮煤层、中部疏松层和顶部较致密层;在微观下主要表现为柱状构造、叠层构造、斑块状构造、纹层状构造等多种类型。富钴结壳的矿物成分主要为自生的铁锰矿物,包括水羟锰矿、钡镁锰矿、羟铁矿、四方纤铁矿、六方纤铁矿、针铁矿等。富钴结壳富含Mn、Fe、Co、Ni、Cu、Pb、Zn等金属元素以及稀土元素和铂族元素,其中Co含量尤为显著。三大洋中,以太平洋富钴结壳的Co平均含量最高。富钴结壳的生长过程极其缓慢,平均仅几毫米每百万年。研究表明,西太平洋富钴结壳最早于始新世-早中新世开始生长。目前通常认为富钴结壳为水成成因,即Co、Fe、Mn等金属元素来源于海水。此外,有研究表明微生物在富钴结壳的形成过程中也起着非常重要的作用。富钴结壳的分布及特征受地形、水深、基岩类型、海水水文化学特征、经纬度等多种因素的影响,其主要分布于碳酸盐补偿深度以上、最低含氧带以下、水深800~2500 m的海山、岛屿斜坡和海底高地上,西、中太平洋海山区被认为是全球富钴结壳的最主要产出区。 相似文献
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富钴铁锰结壳(简称富钴结壳)是产出在海山、岛屿斜坡及海底高地上的一种潜在新型矿产资源,由铁锰氧化物和氢氧化物组成,富含Co、Ni、Zn、Pb、Ce、Pt、REE等金属元素,其中Co的平均含量较陆地原生钴矿高几十倍. 相似文献
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富钴结壳是一种重要的海底矿产资源,具有独特的经济价值和科学意义,其不仅富含Mn、Co、Ni、Cu、PGE和REY等金属,而且在反演新生代以来古海洋环境记录等方面扮演着独特的角色。锰氧化物(MnO2·xH2O)和铁羟基氧化物(FeOOH)是构成富钴结壳的主要矿物,矿物颗粒十分微小(纳米级)。水羟锰矿和水钠锰矿具有层状结构且层电荷为负,通过吸附阳离子来补偿。前人通过连续浸出实验、元素相关性统计分析、吸附实验和拓展X射线吸收精细结构(EXAFS)光谱广泛研究了微量元素在矿物中的赋存状态,确定了微量元素在锰氧化物矿物中主要存在三种类型络合物:共六边(edge-sharing)、共双角(double-corner sharing)和共三角(triple-corner sharing)。综合研究表明,在最低含氧带之下铁锰氧化物(氢氧化物)从海水沉淀到周围海山坚硬基岩上形成富钴结壳的机制主要是无机胶体化学反应和矿物表面反应。最后针对已有的相关研究现状以及富钴结壳研究面临的挑战,富钴结壳的成矿物质来源及演化、微量元素富集机制、蕴含的古海洋信息等问题仍需要进一... 相似文献
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通过针对系统取自中太平洋富钴结壳WXD27的顶部至其底部(1 mm～2 mm为间隔取样)样品进行的Co含量(中子活化方法)测试,拟合出不同深度壳层的富钴结壳生长速率曲线,以此推导富钴结壳Co含量的定年积分公式,并利用10Be定年方法,对Co含量定年的准确性进行检验.时超微量Sr同位素测试得到的富钴结壳磷酸盐年龄进行分析认为:(1)上部富钴结壳与上层白色磷酸盐化层接触部位的年龄为14.9 Ma;(2)自14.9 Ma以来,结壳的生长是连续的,沉积间断发生的可能性非常小,该样品可以用来进行14.9 Ma年以来古海洋、全球变化的重建工作;(3)上层白色磷酸盐化层与其上部的富钴结壳之间存在4 Ma的沉积间断;(4)19 Ma～22.7 Ma左右在该区发生过大规模的磷酸盐化作用,磷酸盐化作用可能造成磷酸盐化时期(19 Ma～22.7 Ma)和之后4 Ma(19 Ma～14.9 Ma)富钴结壳的沉积间断;(5)结壳的初始生长年龄在75 Ma左右;(6)老结壳的生长速度要远低于新结壳的生长速度. 相似文献
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富钴铁锰结壳(简称富钴结壳或海山结壳)是生长在大洋洋底地势较高处(如海山)硬质基岩上的富含铁、锰、钴、铂、稀土等金属元素的"壳状"沉积矿产.与其它深海铁锰沉积相比较,海山结壳的的最主要特征是富Co,其Co含量是大洋铁锰沉积中最高的.但是,同一富钴结壳样品的不同层位Co含量的差异是比较大的,到目前为止,人们并没有充分认识富钴结壳为什么"富钴",即Co发生富集/亏损的原因.本文通过对莱恩海山链MP2海山的一块典型富钴结壳样品电子探针原位化学成分数据的系统分析,对富钴结壳形成过程中Co富集/亏损的原因进行了系统研究,以揭示富钴结壳中的Co富集机制以及富钴结壳成矿作用是否具有时代的特殊性. 相似文献
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采自中太平洋海山富钴结壳主要由水羟锰矿组成,在XRD衍射图谱上,该矿物缺少(001)和(002)底面衍射,其原因是水羟锰矿包含了两种对称型的八面体层,即三斜对称和六方对称的八面体层,它们沿c轴方向无序排列。部分样品中的水羟锰矿在低角度区具有d>2.0nm的超结构衍射峰,它在实质上反映了矿物结构层的长程有序性,即两种层片的排列具有某种周期性或规律性。部分样品原先没有,但在加热后出现超结构衍射峰,可能是因为样品在空气中加热,使三斜层片中的Mn(III)被氧化成Mn(IV),从而转变为六方层片,继而改变了水羟锰矿的有序性。富钴结壳中水羟锰矿的超结构,在一定程度上反映了矿物形成环境的变化。 相似文献
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试谈富钴结壳的成矿机制 总被引：2，自引：0，他引：2
富钴结壳的形成是“物理化学成矿”的结果。在海水中存在一个最低含氧带（OMZ），在此带内，来自内源、外源和水成等多种来源的Fe、Mn等成矿元素含量丰富。在OMZ下方，由于氧化作用，Fe、Mn首先形成水合氧化物胶体，同时Pt也可能在此时从海水中分离出来；在Fe-Mn氧化物沉淀过程中，由于表面吸附作用，具有合适表面电荷的Co^2 、Ni^2 等离子，被吸附到胶体颗粒表面，逐步富集成矿；在微生物和上升海流的作用下，磷酸盐组分加入到结壳中，形成夹层。因此,富钴结壳是多组分分阶段物理化学成矿的产物。 相似文献
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铁锰氧化物矿物胶膜是我国黄棕壤中重要的铁锰元素富集载体,选取我国华中地区典型的铁锰氧化物矿物胶膜样品,采用电感耦合等离子体原子发射光谱(ICP-AES)、偏光显微镜(POM)、环境扫描电子显微镜(ESEM)、能谱仪(EDX)、高分辨透射电子显微镜(HRTEM)、高能量X射线粉末衍射(XRD)等研究方法,对原位和分离处理后的黄棕壤铁锰胶膜进行了详细的矿物学表征.结果表明,黄棕壤铁锰氧化物矿物胶膜由表及里,由外到内依次呈现富锰条带、富铁锰条带、富铁条带、富锰铁条带、富铁条带,并且锰铁元素含量之比不规则降低,其所含铁锰氧化物矿物主要为锰钡矿、针铁矿、水钠锰矿、六方水锰矿、水羟锰矿,粒度为纳米级,形貌多样. 相似文献
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Chemical and structural control of the partitioning of Co, Ce, and Pb in marine ferromanganese oxides 总被引：3，自引：0，他引：3
Yoshio Takahashi Alain Manceau Matthew A. Marcus 《Geochimica et cosmochimica acta》2007,71(4):984-1008
The oxidation state and mineral phase association of Co, Ce, and Pb in hydrogenetic, diagenetic, and hydrothermal marine ferromanganese oxides were characterized by X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy and chemical extraction. Cobalt is trivalent and associated exclusively with the Mn oxide component (vernadite). Cerium is tetravalent in all genetic-type oxides (detection limit for Ce(III) ∼ 5 at. %), including Fe-rich areas (ferrihydrite) of hydrogenetic oxides, and is associated primarily with vernadite. Thus, the extent of a Ce anomaly does not result from variations in redox conditions, but appears to be kinetically controlled, decreasing when the growth rate increases from hydrogenetic to diagenetic to hydrothermal oxides. Lead is divalent and associated with Mn and Fe oxides in variable proportions. According to EXAFS data, Pb is mostly sorbed on edge sites at chain terminations in Fe oxide and at layer edges in Mn oxide (ES complex), and also on interlayer vacancy sites in Mn oxide (TCS complex). Sequential leaching experiments, spectroscopic data, and electrochemical considerations suggest that the geochemical partitioning in favor of the Mn oxide component decreases from Co to Ce to Pb, and depends on their oxidative scavenging by Mn and Fe oxides. 相似文献
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中太平洋YJA海山富钴结壳矿物组成与元素地球化学 总被引：4，自引：3，他引：1
研究样品采自马尔库斯（MARCUS）海脊YJA海山。利用等离子光谱、等离子质谱、X-射线衍射、红外光谱、场发射电镜等分析测试方法,对富钴结壳中不同构造层的矿物组成和元素地球化学进行了研究。该结壳为一大型板状新结壳,矿石矿物是水羟锰矿,脉石矿物是石英、斜长石、磷灰石等,微量矿物有蒙脱石、高岭石、钠沸石、水黑云母、片沸石等。从结壳的底部构造层到顶部构造层,TMn,Ni,Cu, Ba,Zn等元素的质量分数逐渐减少,TFe逐渐增加,Co变化不大;在相对疏松的构造层中,Si,Al,K,Na,Ca,Mg,Ti,P,Li,Rb等元素相对富集;结壳的稀土元素总量是1 982.27×10-6,Ce具明显的正异常。不同构造层稀土元素的演化趋势是：Ce与Mn等元素相同,其他稀土元素（Y除外）与Fe等相似。 相似文献
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Layered ferromanganese crusts collected by dredge from a water depth range of 2770 to 2200 m on Mendeleev Ridge, Arctic Ocean, were analyzed for mineralogical and chemical compositions and dated using the excess 230Th technique. Comparison with crusts from other oceans reveals that Fe-Mn deposits of Mendeleev Ridge have the highest Fe/Mn ratios, are depleted in Mn, Co, and Ni, and enriched in Si and Al as well as some minor elements, Li, Th, Sc, As and V. However, the upper layer of the crusts shows Mn, Co, and Ni contents comparable to crusts from the Atlantic and Indian Oceans. Growth rates vary from 3.03 to 3.97 mm/Myr measured on the uppermost 2 mm. Mn and Fe oxyhydroxides (vernadite, ferroxyhyte, birnessite, todorokite and goethite) and nonmetalliferous detrital minerals characterize the Arctic crusts. Temporal changes in crust composition reflect changes in the depositional environment. Crust formation was dominated by three main processes: precipitation of Fe-Mn oxyhydroxides from ambient ocean water, sorption of metals by those Fe and Mn phases, and fluctuating but large inputs of terrigenous debris. 相似文献
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Cation exchange reactions with participation of heavy metals Mn, Co, Ni, Cu, Zn, Cd, Ba, and Pb were studed in oceanic low-temperature hydrothermal deposits of various mineral compositions and in hydrogenic Fe-Mn crusts. Individual minerals and their assemblages differ significantly in absorptive capacity, which increases in the following order: hematite ? Si-protoferrihydrite < protoferrihydrite < geothite < nontronite ? Fe-vernadite + Mn-feroxyhyte < Fe-free vernadite < bernessite + Fe-free vernadite < bernessite; i.e., it successively increases from the mineral with a coordination type of lattice to minerals with a layer-type structure. The exchange complex of all minerals includes Na+, K+, Ca2+, and Mg2+, i.e., the main cations of seawater. In Mn minerals, Mn2+ is the main exchange component. The contribution of all the mentioned cations to the exchange capacity of minerals is as high as 90–98%. The highest absorptive capacity among the examined low-temperature oceanic deposits is characteristic of hydrothermal Mn minerals. Their capacity exceeds substantially that of hydrothermal oxides, hydroxides, Fe-aluminosilicates, and hydrogenic Fe-Mn minerals. The absorptive capacity of all examined Mn minerals relative to heavy metals increases in the same order: Ni < Zn < Cd < Mn < Co < Pb < Cu. 相似文献
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太平洋北部铁锰结核富集区沉积物的元素地球化学特征 总被引：2，自引：1，他引：2
本文对太平洋北部铁锰结核富集区沉积物的元素地球化学作了较为详细的研究。因子分析提供的信息表明,元素的分布主要受三个因子控制:（1）粘土及Fe、Mn氧化物水化物胶体的吸附作用;（2）生物化学作用过程有关的自生沉积作用;（3）海底页岩风化及附近海区的火山喷发作用。元素的来源:（1）Fe、Mn、Cu、Co、Ni、Zn、Cr、Cr、Mg、Al、Ti、K共生,主要来自粘土吸附;（2）C有机、N、Sr、Na及Si、Ca、Sr主要来自生物化学过程沉积;（3）Pb主要来源于岩石碎屑（火山喷发碎屑）。 相似文献
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The mineralogy of natural ferromanganese coatings on quartz grains and the crystal chemistry of associated trace elements Ni, Zn, Ba, and As were characterized by X-ray microfluorescence, X-ray diffraction, and EXAFS spectroscopy. Fe is speciated as ferrihydrite and Mn as vernadite. The two oxides form alternating Fe- and Mn-rich layers that are irregularly distributed and not always continuous. Unlike naturally abundant Fe-vernadite, in which Fe and Mn are mixed at the nanoscale, the ferrihydrite and vernadite are physically segregated and the trace elements clearly partitioned at the microscopic scale. Vernadite consists of two populations of interstratified one-water layer (7 Å phyllomanganate) and two-water layer (10 Å phyllomanganate) crystallites. In one population, 7 Å layers dominate, and in the other 10 Å layers dominate. The three trace metals Ni, Zn, and Ba are associated with vernadite and the metalloid As with ferrihydrite. In vernadite, nickel is both substituted isomorphically for Mn in the manganese layer and sorbed at vacant Mn layer sites in the interlayer. The partitioning of Ni is pH-dependent, with a strong preference for the first site at circumneutral pH and for the second at acidic pH. Thus, the site occupancy of Ni in vernadite may be an indicator of marine vs. continental origin, and in the latter, of the acidity of streams, lakes, or soil pore waters in which the vernadite formed. Zinc is sorbed only in the interlayer at vacant Mn layer sites. It is fully tetrahedral at a Zn/Mn molar ratio of 0.0138, and partly octahedral at a Zn/Mn ratio of 0.1036 consistent with experimental studies showing that the VIZn/IVZn ratio increases with Zn loading. Barium is sorbed in a slightly offset position above empty tetrahedral cavities in the interlayer. Arsenic tetrahedra are retained at the ferrihydrite surface by a bidentate-binuclear attachment to two adjacent iron octahedra, as commonly observed. Trace elements in ferromanganese precipitates are partitioned at a few, well-defined, crystallographic sites that have some elemental specificity, and thus selectivity. The relative diversity of sorption sites contrasts with the simplicity of the layer structure of vernadite, in which charge deficit arises only from Mn4+ vacancies (i.e., no Mn3+ for Mn4+ substitution). Therefore, sorption mechanisms primarily depend on physical and chemical properties of the sorbate and competition with other ions in solution, such as protons at low pH for Ni sorption. 相似文献
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H. Anawar K. Komaki J. Akai J. Takada T. Ishizuka T. Takahashi T. Yoshioka K. Kato 《Environmental Geology》2002,41(7):816-825
A stratigraphic profile of solid phase As was measured to investigate the diagenetic cycling of arsenic and related elements in fluvial sediments of the Meghna River delta plain. The distributions of Fe, Mn, and Al are typically characterized by surficial solid phase enrichment, and As is distributed down to 36.6 m showing similar alternate layers of maxima and minima with Fe, Mn and TOC, which reflects the diagenetic remobilization and periodical differences in source materials of As. Lithological characteristics and geochemical data suggest that elevated levels of As are found in organic-matter-rich clay and silty sand rather than sand samples, with occasionally enriched As content in iron-oxyhydroxide-coated sand grains. Arsenic demonstrates a positive and significant co-variation with total organic carbon in sediments, which suggests the important role of particulate and colloidal organic matter and biological activity in controlling the distribution of arsenic in the Bengal delta. However, the concentrations of Fe and Mn weakly correlate with As contents, whereas Al contents show no relationship with As. The results of this study suggest that reactive oxides or hydroxides of Fe and Mn, rather than Fe and Mn with other minerals, might control arsenic distribution. 相似文献