中条山—塔儿山成矿区带铜铁金矿床成矿系列组合及成矿模式

中条山一塔儿山成矿区带位于华北与华南断块拼合带北侧之豫皖次级断块西部边缘。中条山区新太古代化到群,古元古代中条群和中元古代西阳河群等火山沉积变质岩系中,分别赋存着不同类型,不同规模的铜（钼,钴,金）矿床,塔儿山区和晋西南区又有与燕山期岩浆热液活动紧密相关的铁,铜,金矿床,古人曾将这个从北至南的成矿区带形象地比喻成一条“铁头,铜腰,金尾巴的巨龙”其中铜（钼,钴,金）矿床形成于华北断志形成阶段：铁（铜     

Study of laser heated iron using third generation synchrotron X-ray radiation facility with imaging plate at high pressures

Iron pressurized to 60 gigapascal (GPa) was heated with laser up to temperatures of over 2200 K. The structural changes were determined in-situ using third generation synchrotron X-ray source; the changes were recorded on an imaging plate with a monochromatic beam. The results strongly support the existence of a phase transformation of the hexagonal close-packed (hcp) structure to the new polymorph (β-phase of iron) at high pressure and temperature. We interpret the X-ray data as belonging to the double hexagonal close-packed (dhcp) structure distorted by stress due to laser heating. Received: 2 February 1998 / Accepted: 23 August 1998     

A comparative study of iron and manganese diagenesis in continental slope and deep sea basin sediments off Uruguay (SW Atlantic)

Pore water and solid phase from surface sediments of the continental slope off Uruguay and from the Argentine Basin (southwestern Atlantic) were investigated geochemically to ascribe characteristic early diagenetic reactions of iron and manganese. Solid-phase iron speciation was determined by extractions as well as by Mössbauer spectroscopy. Both methods showed good agreement ( <6% deviation) for total-Fe speciation. The proportion of easy reducible iron oxyhydroxide relative to total-Fe oxides decreased from the continental slope to the deep sea which is attributed to an increase in crystallinity during transport as well as to a general decrease of iron mobilization. The product of iron reoxidation is Fe oxyhydroxide which made up less than 5% of total Fe. In addition to this fraction, a proportion of smectite bound iron was found to be redox reactive. This fraction made up to 10% of total Fe in sediments of the Argentine Basin and was quantitatively extracted by 1?N HCl. The redox reactive Fe(+II) fraction of smectite was almost completely reoxidized within 24?h under air atmosphere and may therefore considerably contribute to iron redox cycling if bioturbation occurs. In the case of the slope sediments we found concurrent iron and manganese release to pore water. It is not clear whether this is caused by dissimilatory iron and manganese reduction at the same depth or dissimilatory iron reduction alone inducing Mn(+IV) reduction by (abiotic) reaction with released Fe²⁺. The Argentine Basin sediment showed a significant manganese solid-phase enrichment above the denitrification depth despite the absence of a distinct pore-water gradient of Mn. This implies a recent termination of manganese mobilization and thus a non-steady-state situation with respect to sedimentation or to organic carbon burial rate.     

Can fly-ash extend bentonite binder for iron ore agglomeration?

There is great incentive to reduce bentonite use in iron ore pelletization by improving its effectiveness. In order to make bentonite more effective, it is necessary to understand the actual binding mechanisms so that they can be properly taken advantage of. Bentonite use could also be reduced by replacing bentonite with even lower-cost binders, such as high-carbon fly-ash based binder (FBB). While FBBs can be used alone as binders, it was considered possible that mixtures of FBB and bentonite could exhibit superior binding properties. In this study, it was found that bentonite bonds by a physical mechanism, while FBB bonds by a chemical mechanism. These mechanisms were determined to be incompatible. Mixtures of the two binders resulted in reduced dry magnetite concentrate pellet compressive strengths below the industrially acceptable value of 22 N (5 lbf). Activators and accelerators, which were necessary components of the FBB, deactivated the bentonite. The compatibilities and mechanisms of the two binders are explained in this paper. The classical theory of the binding mechanism of bentonite binder is challenged by the bentonite fiber mechanism that was recently identified by the authors.     

Structure and Mössbauer spectroscopy of barbosalite Fe2+Fe3+ 2 (PO4)2(OH)2 between 80 K and 300 K

Natural barbosalite Fe²⁺Fe³⁺ ₂ (PO₄)₂(OH)₂ from Bull Moose Mine, South Dakota, U.S.A., having ideal composition, was investigated with single crystal X-ray diffraction techniques, Mössbauer spectroscopy and SQUID magnetometry to redetermine crystal structure, valence state of iron and evolution of ⁵⁷Fe Mössbauer parameter and to propose the magnetic structure at low temperatures. At 298?K the title compound is monoclinic, space group P2₁/n, a _o ?= 7.3294(16)?Å, b _o ?=?7.4921(17)?Å, c _o ?=?7.4148 (18)?Å, β?=?118.43(3)°, Z?=?2. No crystallographic phase transition was observed between 298?K and 110?K. Slight discontinuities in the temperature dependence of lattice parameters and bond angles in the range between 150?K and 180?K are ascribed to the magnetic phase transition of the title compound. At 298?K the Mössbauer spectrum of the barbosalite shows two paramagnetic components, typical for Fe²⁺ and Fe³⁺ in octahedral coordination; the area ratio Fe³⁺/Fe²⁺ is exactly two, corresponding to the ideal value. Both the Fe²⁺ and the Fe³⁺ sublattice order magnetically below 173?K and exhibit a fully developed magnetic pattern at 160?K. The electric field gradient at the Fe²⁺ site is distorted from axial symmetry with the direction of the magnetic field nearly perpendicular to V_zz, the main component of the electric field gradient. The temperature dependent magnetic susceptibility exhibits strong antiferromagnetic ordering within the corner-sharing Fe³⁺-chains parallel to [101], whereas ferromagnetic coupling is assumed within the face-sharing [1?1?0] and [?1?1?0] Fe³⁺-Fe²⁺-Fe³⁺ trimer, connecting the Fe³⁺-chains to each other.     

Mössbauer and molecular orbital study of chlorites

The different Fe²⁺ lattice sites in iron-rich chlorites have been characterized by Mössbauer spectroscopy and molecular orbital calculations in local density approximation. The Mössbauer measurements were recorded at 77?K within a small velocity range (±3.5?mm?s^?1) to provide high energy resolution. Additionally, measurements were recorded in a wider velocity range (±10.5?mm?s^?1) at temperatures of 140, 200, and 250?K in an applied field (7?T) parallel to the γ-beam. The zero-field spectra were analyzed with discrete Lorentzian-shaped quadrupole doublets to account for the Fe²⁺ sites M1, M2, and M3 and with a quadrupole distribution for Fe³⁺ sites. Such a procedure is justified by the results obtained from MO calculations, which reveal that different anion (OH^?) distributions in the first coordination sphere of M1, M2, and M3 positions have more influence on the Fe²⁺ quadrupole splitting than cationic disorder. The spectra recorded in applied field were analyzed in the spin-Hamiltonian approximation, yielding a negative sign for the electric field gradient (efg) of Fe²⁺ in the M1, M2, and M3 positions. The results of the MO calculations are in quantitative agreement with experiment and reveal that differences in the quadrupole splittings (ΔE _Q ), their temperature dependence and in the isomer shifts (δ) of Fe²⁺ in M1, M2, and M3 positions can theoretically by justified. Therefore, the combined Mössbauer and MO investigation shows that the three Fe²⁺ lattice sites in the chlorites investigated here can be discriminated according to their ΔE _Q -δ parameter pairs. With the calculated average iron-oxygen bond strength, the MO study provides an explanation for the observed trend that the population of the three lattice sites by Fe²⁺ increases according to the relation M1?相似文献   

铁对三角褐指藻生长、光合作用及生化组成的影响

近来许多研究表明,不论是在无机氮丰富还是贫乏的水域,铁元素的供应对于浮游植物的生物量、生长率、种类组成及初级生产力均会产生影响。通过室内培养,研究了铁对三角褐指藻生长、光合作用以及细胞生化组成的影响。实验结果表明,在其他营养盐充足的条件下,海水中铁浓度的变化对三角褐指藻的生长及光合作用均有显着影响。在5×10-7mol/dm3铁浓度时,三角褐指藻可达到其最大光合作用速率。在添加铁的条件下,三角褐指藻细胞多种生化组成受到不同程度的影响,其中叶绿素a含量变化幅度最大,增加了25%～35%,叶绿素c、类胡萝卜素含量也有一定程度的增加,但增长幅度要小于叶绿素a;碳水化合物的含量增加了5%～10%,蛋白质含量的增加幅度在5%～15%之间;超氧化物歧化酶(SOD)的活性及DCMU荧光增强比(F_d/F)也呈明显的增加趋势。铁是海洋初级生产过程中的一种限制因子。     

The Mg-carbonate-Fe interaction:Implication for the fate of subducted carbonates and formation of diamond in the lower mantle

The fate of subducted carbonates in the lower mantle and at the core-mantle boundary was modelled via experiments in the MgCO3-Fe^0 system at 70-150 GPa and 800-2600 Kin a laser-heated diamond anvil cell.Using in situ synchrotro n X-ray diffraction and ex situ transmission electron microscopy we show that the reduction of Mg-carbonate can be exemplified by:6 MgCO3+19 Fe=8 FeO+10(Mg0.6Fe^0.4)O+Fe7 C3+3 C.The presented results suggest that the interaction of carbonates with Fe^0 or Fe^0-bearing rocks can produce Fe-carbide and diamond,which can accumulate in the D"region,depending on its carbon to Fe ratio.Due to the sluggish kinetics of the transformation,diamond can remain metastable at the core-mantle boundary(CMB)unless it is in a direct contact with Fe-metal.In addition,it can be remobilized by redox melting accompanying the generation of mantle plumes.     

铁矿开采对地下水环境影响评价实证研究

铁矿开采与地下水紧密联系,不仅会影响地下水资源,而且还会破坏地下水的动态平衡和生态环境。结合某铁矿开采项目实际,依据地下水环境评价导则,在分析铁矿区地下水水质、水文地质条件等资料的基础上,预测评价铁矿开采对地下水水质、水量等方面的影响,提出地下水环境保护措施。     

Implications of Pb isotope signatures of rocks and iron oxide Cu-Au ores in the Candelaria-Punta del Cobre district,Chile

Lead isotope ratios of ores of the Candelaria-Punta del Cobre iron oxide Cu-Au deposits and associated Early Cretaceous volcanic and batholithic rocks have been determined. For the igneous rocks, a whole-rock acid attack technique based on the separate analyses of a leachate and the residual fraction of a sample was used. The lead isotope systematics of leachate–residue pairs are significantly different for unaltered and altered igneous rocks of the Candelaria-Punta del Cobre district. Residues of unaltered igneous rocks likely represent the common lead. In contrast, residues of all the altered igneous rocks except two samples have higher Pb isotope ratios than those of unaltered magmatic rocks and cannot represent common lead. We suggest that this is a result of the hydrothermal alteration suffered by these rocks and that the common lead composition of the altered igneous (volcanic and plutonic) rocks must have been similar to that of the unaltered batholith rocks. The conclusion that the altered volcanic rocks originally had a similar common lead isotope composition as the batholith is consistent with geological and geochemical arguments (e.g., setting, regional geologic evolution, ages and relative distribution of volcanic and intrusive rocks, magmatic affinities), which indicate that these rocks were derived from similar Early Cretaceous parent magmas. The modification of the leachate–residue pair lead isotope systematics of most altered igneous rocks is consistent with a selective removal of lead and uranium from these rocks by an oxidized hydrothermal fluid. The result of the hydrothermal leaching has been to alter magmatic rocks in a way that (1) their leachable fraction is presently a mix of common lead similar to that of the ore event and of radiogenic lead evolved from a source with a consistently high Th/U, and that (2) their residual fraction has less common lead than unaltered rocks. The outcrop area with altered volcanic rocks displaying anomalously high lead isotope ratios extends over 25 km along the eastern margin of the batholith. Since lead of the ores in the Candelaria-Punta del Cobre district has the same isotopic composition as the common lead of unaltered magmatic rocks of the area, the lead isotope data are consistent with a derivation of the ore lead (and by inference of other metals like Cu) both directly from a magmatic fluid exsolved during crystallization of the batholith and/or from hydrothermal leaching of the volcanic rocks originally having similar isotopic compositions as the batholith.Editorial handling: B. Lehmann