榴辉岩中铁铝榴石的测定方法研究   总被引：3，自引：1，他引：3  

黄宝贵  柳建春 《岩矿测试》1997,16(4):241-244254

对国内主要矿区铁铝石榴子石纯矿物中铁的价态规律进行了研究。证明其所含Ｆｅ均以Ｆｅ＾２＋为主，其质量分数在８３－９４，并将Ｆｅ＾２＋这特征性成分用于某地榴辉岩中铁铝榴石的间接测定，获得结果与焙烧磁化－磁选法一致且精度好，较磁化法简便，快速。  相似文献   

低温条件下有机酸对铁、铜的淋滤实验研究     

张海祥  王玉荣  梅厚钧 《矿床地质》1997,16(1):86-92

水／岩作用实验研究表明，在低温条件下柠檬酸、草酸和酒石酸对岩石中的铁、铜都有很高的淋滤率。这表明，在表生地质作用过程中有机酸对成矿元素有很强的活化能力。实验研究同时发现，有机酸对成矿元素的活化能力受其分解温度的限制，由于大部分有机酸的分解温度都在２５０℃以下，因而有机酸对成矿元素的活化仅限于低温条件。本次研究还显示，判断一种岩石能否成为矿源层，不能简单的以其中成矿元素的含量高低作为标准，其中更关键的因素是元素在岩石中的存在形式，如果成矿元素在岩石中难以活化的形式存在，那么含量再高也无法提供成矿物质  相似文献   

西昆仑山南侧甜水海湖岩芯铁变化的环境记录   总被引：11，自引：0，他引：11  

余素华  李世杰 《地球化学》1997,26(6):88-98

阐述了青藏高原西昆仑山南侧甜水海湖岩芯沉积物中氧化铁的丰度、频率分布和富集系数的变化规律。其丰度值范围FeO0．39％-3.95％，平均值为1．25％；Fe2O30．44％－8．09％，平均值为2．60％；Fe2O3／FeO0．21－3．60，平均比值1．12。说明该彻岩芯沉积物中铁平均丰度值较低，但其变化幅度较宽且清楚，在一定程度上反映了古气候环境具有较大幅度的波动。变异系数值表明，该湖岩芯沉积物中FeO的离散程度较Fe2O3大。大约距今23万年来氧化铁的沉积地球化学特征可划分出7个环境演化阶段，并基本上可与深海氧同位索阶段对比。揭示了甜水海湖演化与青藏高原强烈隆升引起的气候环境改变的密切关系。在距今23一15万年，沉积以河流相或冲积、洪积相为主，沉积环境以氧化环境为主导，气候以温干型波动；在距今15－7．4万年，沉积以湖相为主，沉积环境以还原环境为主导，气候以温湿型为主；在距今74万年以来，湖盆沉积环境多样化，沉积物以湖相和近源冲积、洪积相交替出现。气候出现冷湿、冷干、温湿和温干多种波动模式。这些资料分析初步认为甜水海古湖大约形成于距今15万年，即青藏高原第三成湖期，这也与青藏高原在距今15万年左右的再次构造隆升有关。  相似文献   

Yixunite and Damiaoite—A Twin of New Native Alloys of Indium and Platinum from the Yanshan Mountains     

Yu ZuxiangInstitute of Geology  Chinese Academy of Geological Sciences  Baiwanzhuan  Beijing 《《地质学报》英文版》1997,71(4):480-485

Yixunite and damiaoite Were found in a cobalt- and copper-bearing platinum ore vein of a contact metasomatic deposit. The chief ore minerals are bornite, chalcopyrite, magnetite and carrollite. The platinum minerals include moncheite, sperrylite, daomanite, cobalt malanite and cooperite. Yixunite and damiaoite occur as immiscible globules, 1.0 to 2.0 mm in diameter. Yixunite is always in the central part of a globule. It is opaque with metallic lustre, bright white colour and black streak. HM = 5.8; VHN50 = 634 kg/mm2 (573-681 kg/ mm2); insoluble in HCl, HNO3, HF or H3PO4; no cleavage; no magnetism. Density is hard to measure because of small grain size. Calculated density = 18.21 g/cm3. Reflective colour is bright white with a yellowish tint. Isotropic. The mean analytical results (ranges) (%) are: Pt 82.8 (81.8-83.6), In 16.4(15.6-17.1) and total 99.2. The empirical formula (based on 4 atoms) is Pt2.993 In1.007 . The five strongest lines of X-ray diffraction (hkl, d,I) are 111, 2.30 (100); 200, 1.99 (  相似文献   

Iron oxidation state in lower mantle mineral assemblages: II. Inclusions in diamonds from Kankan, Guinea     

C.A McCammon  T Stachel 《Earth and Planetary Science Letters》2004,222(2):423-434

Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O₃ perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe³⁺/ΣFe. Fe³⁺ concentration in the (Mg,Fe)(Si,Al)O₃ inclusion is consistent with empirical relations relating Fe³⁺/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na_0.5M_0.5³⁺O (M=Fe³⁺, Cr³⁺, Al³⁺). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO₂ equilibrium. Fe²⁺/Mg partition coefficients between (Mg,Fe)(Si,Al)O₃ and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe³⁺ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ¹³C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe³⁺ concentration in (Mg,Fe)(Si,Al)O₃ perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.  相似文献   

Occurrence of Halogen-rich Phlogopite in Late Cenozoic Volcanic Rocks in the Japanese Arcs     

Akira Imai 《Resource Geology》2004,54(2):153-166

Abstract. Halogen-rich phlogopite occurs in the groundmass of andesite and dacite lavas from Late Tertiary to Quaternary volcanoes associated with native sulfur and limonite deposits (Shiretoko-Iwozan, Hachimantai, Adatara, Omeshidake, Masaki) and hydrothermal ore deposits (Harukayama, Muineyama, Hishikari) in Japan. The F contents of the halogen-rich phlogopite range from 3.6 to 5.7 wt%, corresponding to atomic F/(F+C1+OH) ratios ranging from 0.45 to 0.69. On the other hand, the Cl contents of the halogen-rich phlogopite are around 0.2 wt%. The atomic Mg/(Mg+Fe) ratios range from 0.69 to 0.83.
The fluorine intercept value [IV(F)] defined by Munoz (1984) of the phlogopites ranges from 0.79 to 3.17, and the chlorine intercept value [IV(Cl)] ranges from -7.11 to -7.77. The observed IV(F) of the phlogopites broadly overlap the range of the IV(F) for biotites from porphyry copper deposits. On the other hand, the observed IV(Cl) are significantly lower than the IV(Cl) for biotites from porphyry copper deposits. Whereas the F contents of the phlogopite appear more prominent compared to the Cl contents, the calculation of halogen intercept values revealed that the phlogopites are enriched in Cl with respect to the element distribution effect of Mg-Fe substitution. Since the degree of Cl enrichment of the phlogopite is more significant compared to that of biotite in porphyry copper deposits, the phlogopites are considered to have formed under the condition of significantly high activity of halogens. Hydrothermal ore deposits may be formed in magmatic hydrothermal system associated with volcanoes where halogen-rich phlogopite is formed by hypersaline fluid.  相似文献   

Effet de la teneur en eau d'un sol sur la réduction bactérienne d'oxydes de fer     

Sébastien J. Stemmler  Stéphanie Loyaux-Lawniczak  Jacques Berthelin 《Comptes Rendus Geoscience》2004,336(13):1171-1179

Iron-reducing activity of autochthonous bacteria from two temporary hydromorphic soils is evaluated by the study of iron reductive dissolution, as a function of water content. The release of ferrous iron in solution is coupled to the mineralization of soil organic carbon. Water soil saturation is not necessary for iron reductive dissolution, since the highest dissolution is obtained for a wet, but not water-saturated soil (100% of water holding capacity WHC), and dissolution is also very high in a soil at 75% WHC. To cite this article: S.J. Stemmler et al., C. R. Geoscience 336 (2004).  相似文献   

Dust production and the release of iron oxides resulting from the aeolian abrasion of natural dune sands     

Joanna E. Bullard  Kevin White 《地球表面变化过程与地形》2005,30(1):95-106

Global dust trajectories indicate that signi?cant quantities of aeolian‐transported iron oxides originate in contemporary dryland areas. One potential source is the iron‐rich clay coatings that characterize many sand‐sized particles in desert dune?elds. This paper uses laboratory experiments to determine the rate at which these coatings can be removed from dune sands by aeolian abrasion. The coatings impart a red colour to the grains to which previous researchers have assigned variable geomorphological signi?cance. The quantities of iron removed during a 120 hour abrasion experiment are small (99 mg kg^?1) and dif?cult to detect by eye; however, high resolution spectroscopy clearly indicates that ferric oxides are released during abrasion and the re?ectance of the particles alters. One of the products of aeolian abrasion is ?ne particles (<10 µm diameter) with the potential for long distance transport. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

Local provenance in rehabilitation of degraded landscapes: a case study from the Hawkesbury–Nepean catchment, Australia     

Shelley Burgin  J Carson  B Maheshwari 《Area》2005,37(3):324-331

Throughout Australia thousands of volunteers are engaged in Landcare projects that should help rehabilitate degraded landscapes. Many of these projects involve tree planting, but their seed is not necessarily of local provenance. Based on a survey of 85 Landcare groups working in the Hawkesbury–Nepean catchment, data were collected about Landcare groups' knowledge of their seed source, understanding of local provenance and the ecosystem in which they were planting trees and the source of funding for their projects. The findings from the study indicate that about one in five (21%) of the groups surveyed that introduced plant material were not aware of local provenance issues. Indirect indications were that a large number of Landcare groups state-wide may be doing more harm than good to the landscape while trying to rehabilitate it. The data also showed that one in seven (13%) of the groups funded by the Australian Government through the Natural Heritage Trust (NHT) had limited awareness of local provenance issues. With millions of dollars being spent on 'works on the ground', it would be prudent to allocate some funds to document and monitor current Landcare activities, so that the environmental outcomes can be quantified and more effective Landcare policies can be developed in the future.  相似文献   

Development of a reactive zone technology for simultaneous in situ immobilisation of radium and uranium     

D. Burghardt  A. Kassahun 《Environmental Geology》2005,49(2):314-320

Simultaneous in situ immobilisation of uranium (U) and radium (²²⁶Ra) by injectible amounts of grey cast iron (gcFe), nano-scale iron (naFe) and a gcFe/MnO₂ mixture (1:1) was studied in batch and column tests. Both 0.5 g/L naFe and gcFe are effective in ²²⁶Ra and U removal from mine water, whereas MnO₂ addition clearly increased the efficiency of gcFe for ²²⁶Ra and U immobilisation. In a column test with 0.6 wt% gcFe/MnO₂ mixture (1:1), neither ²²⁶Ra nor U was detected in the effluent after replacement of 45 pore volumes. A sequential extraction under flow condition revealed ²²⁶Ra to be mostly occluded in manganese oxides. Uranium was mostly sorbed onto poorly crystalline iron hydroxides, but a significant part was found to be occluded in manganese oxides also. The results of this study suggest that MnO₂ promotes iron hydroxide formation under slightly reducing environmental conditions resulting in an increased pollutant retention capacity.  相似文献