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51.
52.
鞍山齐大山铁矿王家堡子采区产出鞍山式沉积变质型铁矿,铁矿石多以磁铁贫矿为主,局部产出富铁矿,目前钻探工程控制标高为-600 m,采区深部的资源潜力是急待解决的问题,为此对采区进行音频大地电磁测量和研究工作。齐大山铁矿的电性变化复杂,通过先期的实验剖面确定了矿区铁矿体的3种不同电阻率特征,然后对王家堡子采区的3760线、4050线、4500线进行音频大地电磁测量、数据处理和断面反演分析。推测3760线的低阻由磁铁贫矿引起,局部高阻为假象赤铁贫矿引起;推测4050线和4500线浅部的低阻由磁铁贫矿引起,深部的高阻为假象赤铁贫矿及磁铁贫矿引起。同时预测3760线、4050线和4500线西侧深部均有低电阻率显示,反映出隐伏铁矿床的存在特征,推测在-1 000 m标高以下仍存在有隐伏的富矿体或板状磁铁贫矿。经过钻探验证,获得了预期的找矿效果。 相似文献
53.
54.
Frédéric Moynier Toshiyuki Fujii Kun Wang Julien Foriel 《Comptes Rendus Geoscience》2013,345(5-6):230-240
Iron is one of the most abundant transition metal in higher plants and variations in its isotopic compositions can be used to trace its utilization. In order to better understand the effect of plant-induced isotopic fractionation on the global Fe cycling, we have estimated by quantum chemical calculations the magnitude of the isotopic fractionation between different Fe species relevant to the transport and storage of Fe in higher plants: Fe(II)-citrate, Fe(III)-citrate, Fe(II)-nicotianamine, and Fe(III)-phytosiderophore. The ab initio calculations show firstly, that Fe(II)-nicotianamine is ~3‰ (56Fe/54Fe) isotopically lighter than Fe(III)-phytosiderophore; secondly, even in the absence of redox changes of Fe, change in the speciation alone can create up to ~1.5‰ isotopic fractionation. For example, Fe(III)-phytosiderophore is up to 1.5‰ heavier than Fe(III)-citrate2 and Fe(II)-nicotianamine is up to 1‰ heavier than Fe(II)-citrate. In addition, in order to better understand the Fe isotopic fractionation between different plant components, we have analyzed the iron isotopic composition of different organs (roots, seeds, germinated seeds, leaves and stems) from six species of higher plants: the dicot lentil (Lens culinaris), and the graminaceous monocots Virginia wild rye (Elymus virginicus), Johnsongrass (Sorghum halepense), Kentucky bluegrass (Poa pratensis), river oat (Uniola latifolia), and Indian goosegrass (Eleusine indica). The calculations may explain that the roots of strategy-II plants (Fe(III)-phytosiderophore) are isotopically heavier (by about 1‰ for the δ56Fe) than the upper parts of the plants (Fe transported as Fe(III)-citrate in the xylem or Fe(II)-nicotianamine in the phloem). In addition, we suggest that the isotopic variations observed between younger and older leaves could be explained by mixing of Fe received from the xylem and the phloem. 相似文献
55.
碳酸盐岩的Fe/Mn元素比值,作为一项新的地球化学指标,可以用于恢复海洋的氧化还原状态.在氧化条件下,Fe3+和Mn4+均不可溶,因此氧化海水中的溶解Fe和Mn的含量均很低.Fe3+和Mn4+在还原条件下可以被细菌还原为可溶的Fe2+和Mn2+,而氧化还原电位的计算表明,Mn4+的还原要早于Fe3+的还原,因此细菌的Mn还原过程发生在沉积物的更浅层.可溶的Fe2+和Mn2+向上扩散到海水中,替代碳酸盐岩晶格里的Ca2+,因此碳酸盐岩晶格中的Fe2+和Mn2+的含量受控于来自沉积物孔隙水的扩散,而后者又与水岩界面的氧化还原状态相关.因此可以预测,随着海水变得逐渐缺氧,碳酸盐岩中的Fe/Mn比值会逐渐增高.为了验证这一假说,我们分析了中元古代高于庄组白云岩的Fe/Mn比值.研究发现,几乎所有的样品的Fe/Mn比值介于20~30之间,显著高于泥盆纪末期深水碳酸盐岩和浅水台地碳酸盐岩的Fe/Mn比值.高于庄组碳酸盐岩高的Fe/Mn比值一方面可能指示了中元古代低的大气氧气浓度和海洋的广泛缺氧,也可能反映了白云岩形成于缺氧的沉积物空隙水里. 相似文献
56.
Authigenic albites in carbonate rocks typically grow in a high-grade diagenetic to low-grade metamorphic environment and often show Roc-Tourné-twinning sensu Füchtbauer. Based on an investigation of four Middle to South European occurrences, they show Mn2+- and Fe3+-activated cathodoluminescence (CL), as revealed by combined high resolution spectroscopy of cathodoluminescence emission (HRS-CL), electron paramagnetic resonance (EPR), and proton-induced X-ray emission (μPIXE). 相似文献
57.
Abstract: A strange, unidentified, Cu-Fe bearing zinc sulfide occurs in the Laloki massive sulfide deposit, Papua New Guinea. The mineral is optically uniform in texture but is chemically variable and zoned even within a single grain. Copper contents vary from 0.1 up to 8.85 wt%. Iron reaches 18.31 wt% at maximum and decreases as Cu increases. It is remarkable, however, that the total Fe+Cu remains essentially unchanged between roughly 18 and 20 wt%. Zn and S are least variable, giving 45.85–47.84 wt% and 33.48–34.58 wt%, respectively. Other trace elements such as Cd and Mn are in general less than 0.2 wt%. It is strongly suggested that the mineral in question constitutes a unique Fe-Cu substitutional solid solution series belonging essentially to the Zn–Fe–Cu–S system.
The ideal chemical formula of the solid solution series can well be presented as Zn10 (Fe, Cu)5 S15 or Zn2 (Fe, Cu)S3 , where Fe is always greater than Cu. It is intriguing that chalcopyrite blebs are recognizable restrictively only in nearby portions of the Cu-rich end member with the ideal composition close to Zn10 Fe3 Cu2 S15. It has been confirmed by vacuum-sealed heating experiments that this mineral is decomposed to produce chalcopyrite and Fe-bearing normal sphalerite at temperatures below 200C. This would provide another evidence for the existence of such distinct phase as suggested here. 相似文献
The ideal chemical formula of the solid solution series can well be presented as Zn
58.
安徽姑山矿浆型铁矿床Fe同位素初步研究 总被引:2,自引:0,他引:2
文章报道了宁芜矿集区内姑山矿浆型铁矿床中的铁氧化物、辉石闪长玢岩和赋矿围岩的Fe同位素组成,其δ57Fe的总体分布范围为-0.05‰~0.79‰。结果显示,姑山铁矿床的铁氧化物赤铁矿和镜铁矿均比硅酸盐岩浆结晶产物(辉石闪长岩)富集重的Fe同位素,并且硅酸盐岩浆的Fe同位素组成比已报道的火山岩的平均Fe同位素组成更富集轻的Fe同位素,表明在岩浆不混溶的过程中Fe同位素发生了分馏,富铁熔体相对富集重的Fe同位素,而硅酸盐熔体相对富集轻的Fe同位素;相对于赋矿地层(黄马青组石英砂岩)和辉石闪长玢岩,赤铁矿和镜铁矿更富集重的Fe同位素,围岩地层和闪长岩岩体则富集轻的Fe同位素。因此,姑山铁矿床的铁质不大可能来自于地层或闪长玢岩岩体,而主要来源于深部岩浆房。 相似文献
59.
Breakdown of hydrous ringwoodite to pyroxene and spinelloid at high P and T and oxidizing conditions
To get deeper insight into the phase relations in the end-member system Fe2SiO4 and in the system (Fe, Mg)2SiO4 experiments were performed in a multi-anvil apparatus at 7 and 13 GPa and 1,000–1,200°C as a function of oxygen fugacity.
The oxygen fugacity was varied using the solid oxygen buffer systems Fe/FeO, quartz–fayalite–magnetite, MtW and Ni/NiO. The
run products were characterized by electron microprobe, Raman- and FTIR-spectroscopy, X-ray powder diffraction and transmission
electron microscopy. At fO2 corresponding to Ni/NiO Fe-ringwoodite transforms to ferrosilite and spinelloid according to the reaction: 9 Fe2SiO4 + O2 = 6 FeSiO3 + 5 Fe2.40Si0.60O4. Refinement of site occupancies in combination with stoichiometric Fe3+ calculations show that 32% of the total Fe is incorporated as Fe3+ according to From the Rietveld refinement we identified spl as spinelloid III (isostructural with wadsleyite) and/or spinelloid V. As
we used water in excess in the experiments the run products were also analyzed for structural water incorporation. Adding
Mg to the system increases the stability field of ringwoodite to higher oxygen fugacity and the spinel structure seems to
accept higher Fe3+ but also water concentrations that may be linked. At oxygen fugacity corresponding to MtW conditions similar phase relations
in respect to the breakdown reaction in the Fe-end-member system were observed but with a strong fractionation of Fe into
spl and Mg into coexisting cpx. Thus, through this strong fractionation it is possible to stabilize very Fe-rich wadsleyite
with considerable Fe3+ concentrations even at an intermediate Fe–Mg bulk composition: assuming constant K
D independent on composition and a bulk composition of x
Fe = 0.44 this fractionation would stabilize spl with x
Fe = 0.72. Thus, spl could be a potential Fe3+ bearing phase at P–T conditions of the transition zone but because of the oxidizing conditions and the Fe-rich bulk composition
needed one would expect it more in subduction zone environments than in the transition zone in senso stricto.
相似文献
M. Koch-MüllerEmail: |
60.
Jin Li Suo‐han Tang Xiang‐kun Zhu Zhi‐hong Li Shi‐Zhen Li Bin Yan Yue Wang Jian Sun Yao Shi Aiguo Dong Nick S. Belshaw Xingchao Zhang Sheng‐ao Liu Ji‐hua Liu Deli Wang Shao‐yong Jiang KeJun Hou Anthony S. Cohen 《Geostandards and Geoanalytical Research》2019,43(1):163-175
Iron, Cu and Zn stable isotope systems are applied in constraining a variety of geochemical and environmental processes. Secondary reference materials have been developed by the Institute of Geology, Chinese Academy of Geological Sciences (CAGS), in collaboration with other participating laboratories, comprising three solutions (CAGS‐Fe, CAGS‐Cu and CAGS‐Zn) and one basalt (CAGS‐Basalt). These materials exhibit sufficient homogeneity and stability for application in Fe, Cu and Zn isotopic ratio determinations. Reference values were determined by inter‐laboratory analytical comparisons involving up to eight participating laboratories employing MC‐ICP‐MS techniques, based on the unweighted means of submitted results. Isotopic compositions are reported in per mil notation, based on reference materials IRMM‐014 for Fe, NIST SRM 976 for Cu and IRMM‐3702 for Zn. Respective reference values of CAGS‐Fe, CAGS‐Cu and CAGS‐Zn solutions are as follows: δ56Fe = 0.83 ± 0.07 and δ57Fe = 1.20 ± 0.13, δ65Cu = 0.57 ± 0.06, and δ66Zn = ?0.79 ± 0.12 and δ68Zn = ?1.65 ± 0.24, respectively. Those of CAGS‐Basalt are δ56Fe = 0.15 ± 0.07, δ57Fe = 0.22 ± 0.10, δ65Cu = 0.12 ± 0.08, δ66Zn = 0.17 ± 0.13, and δ68Zn = 0.34 ± 0.26 (2s). 相似文献