微生物作用下玄武岩的溶解: 粘附作用和温度的影响

使用透析的方法,设计实验探讨了多粘芽孢杆菌(Paenibacillus polymyxa)的粘附对玄武岩中矿物溶解的影响,同时通过改变实验温度,探讨了岩石的微生物溶解与温度的关系.10 d的实验结果表明,在30 ℃条件下,细菌P. polymyxa及其代谢产物对玄武岩的溶解有显著促进作用,加速了橄榄石中Mg、Fe、Mn的溶出及辉石和长石中Ca、Al的溶出,而在5℃条件下,这种促进作用不明显.细菌及其代谢物的粘附能加速Mg、Fe、Mn的溶出,抑制Ca的溶出,这种不同的影响与两组元素的溶出机制不同,且粘附对各溶出机制的影响也不同有关,Al的溶出受粘附作用的影响较小.低温条件下,粘附作用对玄武岩中各元素的溶出基本无影响.     

Importance of hydrogeological conditions during formation of the karstic bauxite deposits,Central Guizhou Province,Southwest China: A case study at Lindai deposit

Karstic bauxite deposits are widespread in Central Guizhou Province, SW China, and high-grade ores are frequently sandwiched with overlying coal and underlying iron-rich layers and form a special “coal–bauxite–iron” structure. The Lindai deposit, which is one of the most representative karstic bauxite deposits in Central Guizhou Province, was selected as a case study. Based on textural features and iron abundances, bauxite ores in the Lindai deposit are divided into three types of ores, i.e., clastic, compact, and high-iron. The bauxite ores primarily comprise diaspore, boehmite, kaolinite, illite, and hematite with minor quartz, smectite, pyrite, zircon, rutile, anatase, and feldspar. The Al₂O₃ (53–76.8 wt.%) is the main chemical contents of the bauxite ore samples in the Lindai district, followed by SiO₂, Fe₂O₃, TiO₂, CaO, MgO, S, and P etc. Our geological data on the Lindai deposit indicated that the ore-bearing rock series and its underlying stratum have similar rare earth elements distribution pattern and similar Y/Ho, Zr/Hf, and Eu/Eu¹ values; additionally, all ore-bearing rock samples are rich in MgO (range from 0.16 wt.% to 0.68 wt.%), and the plots of the dolomites and laterites lie almost on or close to the weathering line fit by the Al-bearing rocks in Zr vs. Hf and Nb vs. Ta diagrams; suggesting that the underlying Middle Cambrian Shilengshui Formation dolomite is the parent rock of bauxite resources in the Lindai district.Simulated weathering experiments on the modern laterite from the Shilengshui Formation dolomite in the Lindai bauxite deposit show that hydrogeological conditions are important for karstic bauxite formation: Si is most likely to migrate, its migration rate is several magnitudes higher than those of Al and Fe under natural conditions; the reducing inorganic acid condition is the most conducive to Al enrichment and Si removal; Fe does not migrate easily in groundwater, Al enrichment and Fe removal can occur only in acidic and reducing conditions with the presence of organic matter.The geological and experimental studies show that “coal–bauxite–iron” structure in Lindai deposit is formed under certain hydrogeological conditions, i.e., since lateritic bauxite or Al-rich laterite deposited upon the semi-closed karst depressions, Si can be continuously removed out under neutral/acidic groundwater conditions; the coal/carbonaceous rock overlying the bauxitic materials were easily oxidized to produce acidic (H₂S, H₂SO₄, etc.) and reductant groundwater with organic materials that percolated downward, resulting in enrichment of Al in underlying bauxite; it also reduced Fe³⁺ to its easily migrating form Fe²⁺, moving downward to near the basal carbonate culminated in precipitating of ferruginous (FeS₂, FeCO₃, etc.) strata of the “coal–bauxite–iron” structure. Thus, the bauxitic materials experienced Al enrichment and Si and Fe removal under above certain hydrogeological conditions forming the high-quality bauxite.     

贵州新民铝土矿矿床Li的地球化学特征与富集机制探究

新民铝土矿床位于黔北务川-正安-道真地区(简称务正道地区)大塘向斜东翼,铝土矿(岩)型Li资源丰富.含矿岩系大竹园组(P1d)不同岩性的w(Li)有差别:土状-半土状铝土矿平均w(Li)为16.34×10-6,致密块状铝土矿平均w(Li)是803.84×10-6,铝土岩平均w(Li)是1436.22×10-6,黏土岩的平均w(Li)是786.62×10-6,梁山组泥岩的平均w(Li)是51.82×10-,韩家店群泥岩(页岩)的平均w(Li)是48.52×10-6,黄龙组灰岩的平均w(Li)是 11.99×10-6.由此可知,研究区铝土矿(岩)型Li资源主要富集在含矿岩系中上部的致密块状铝土矿、铝土岩和黏土岩中,顶板、底板以及土状-半土状铝土矿w(Li)较低.Li主要赋存于高岭石中,伊利石(水云母)和残存的三水铝石、勃姆石也可富集少量Li,当样品中赋锂矿物(高岭石、伊利石(水云母)、三水铝石和勃姆石)都存在时,高w(Li),主量元素w(Al3O2)、w(SiO2)、w(MgO)、w(K2O)、w(TiO2)和w(TFe2O3)与w(Li)的相关性也证实了上述结果.研究区的地球化学比值 CIA、w(Sr)/w(Cu)、u(CaO)/w(MgO)、w(Sr)/w(Ba)、w(V)/w(V+Ni)和 w(La)/w(Y)综合显示,炎热潮湿的古气候下,有机质腐烂形成酸性环境,半封闭海湾环境下,黏土化阶段中等强烈的化学风化程度和适宜的风化暴露剥蚀时间利于铝硅酸盐矿物和硅酸盐矿物化学键断裂,富集Al3+形成高岭石;风化程度过于强烈和长时间的风化剥蚀,继续脱Si富Al形成以硬水铝石为主的铝土矿;弱酸性-弱碱性以及氧化-还原过渡条件下,使得高岭石能最大程度的吸附Li元素.     

桂西平果教美矿区堆积型铝土矿形成过程中矿物转化与元素迁移

桂西地区铝土矿为典型喀斯特型,包括二叠系沉积型和第四系堆积型两亚类。堆积型铝土矿是沉积型铝土矿经抬升、破碎、风化,最后堆积于喀斯特洼地中形成。以平果教美铝土矿为研究对象,探索堆积型铝土矿形成过程中矿物的变化与元素迁移。沉积型矿石的矿物组成包括硬水铝石、鲕绿泥石、锐钛矿及少量针铁矿、金红石和高岭石;堆积型矿石的矿物组成主要为硬水铝石、锐钛矿、高岭石及少量三水铝石和鲕绿泥石。转化过程中堆积型矿石中的硬水铝石含量明显增加,鲕绿泥石含量明显减少。沉积型铝土矿的主要化学组成为Al₂O₃、SiO₂、FeO和TiO₂;堆积型为Al₂O₃、SiO₂、TiO₂和Fe₂O₃。两类矿石中元素Zr 、Ba、Nb、V含量均较高,稀土总量变化大,富集轻稀土。质量平衡计算表明堆积型铝土矿形成过程中Al、Ba、Sr、Y等元素增加,而Si、Fe、Ti、Nb、V、Ce等元素减少,其余元素变化不明显。     

The effect of Fe on Si adsorption by Bacillus subtilis cell walls: insights into non-metabolic bacterial precipitation of silicate minerals

Si adsorption onto Bacillus subtilis and Fe and Al oxide coated cells of B. subtilis was measured both as a function of pH and of bacterial concentration in suspension in order to gain insight into the mechanism of association between silica and silicate precipitates and bacterial cell walls. All experiments were conducted in undersaturated solutions with respect to silicate mineral phases in order to isolate the important adsorption reactions from precipitation kinetics effects of bacterial surfaces. The experimental results indicate that there is little association between aqueous Si and the bacterial surface, even under low pH conditions where most of the organic acid functional groups that are present on the bacterial surface are fully protonated and neutrally charged. Conversely, Fe and Al oxide coated bacteria, and Fe oxide precipitates only, all bind significant concentrations of aqueous Si over a wide range of pH conditions. Our results are consistent with those of Konhauser et al. [Geology 21 (1993) 1103; Environ. Microbiol. 60 (1994) 49] and Konhauser and Urrutia [Chem. Geol. 161 (1999) 399] in that they suggest that the association between silicate minerals and bacterial surfaces is not caused by direct Si–bacteria interactions. Rather, the association is most likely caused by the adsorption of Si onto Fe and Al oxides which are electrostatically bound to the bacterial surface. Therefore, the role of bacteria in silica and silicate mineralization is to concentrate Fe and Al through adsorption and/or precipitation reactions. Bacteria serve as bases, or perhaps templates, for Fe and Al oxide precipitation, and it is these oxide mineral surfaces (and perhaps other metal oxide surfaces as well) that are reactive with aqueous Si, forming surface complexes that are the precursors to the formation of silica and silicate minerals.     

Transformation from Permian to Quaternary bauxite in southwestern South China Block driven by superimposed orogeny: A case study from Sanhe ore deposit

Permian karstic bauxite and its Quaternary derivative, in western Guangxi, southwestern, South China Block, possess a total tonnage greater than 0.5 billion tons. The primary late Permian karstic bauxite formed in reduced environment in the background of Tethyan accretionary orogenesis. And as one consequence of Cenozoic convergence of the Indian and Eurasia continents, the primary orebody was uplifted, eroded and re-sedimented within Quaternary laterite. The geochemical variation and its controls during the ore transformation from Permian to Quaternary remain poorly understood. Quaternary ore blocks comprise an inner zone of fresh ore, and then it gradually transited through a middle zone to a margin with extensive weathering. One such bauxite block was selected and further subdivided into twenty-three samples for geochemical and mineralogical analysis. The inner and middle zones contain similar mineralogical compositions, dominated by diaspore and amesite, with minor illite, anatase, goethite, pyrite, zircon, and rutile. The margin is composed of diaspore, with small amounts of amesite, boehmite, illite, goethite, anatase, kaolinite, zircon, rutile, and barite. Bauxite in all three zones is composed of mainly Al, Si, Fe, and Ti, and high contents of Zr, Cr, Li, F, S, Zn, V, Sr, Nb, Ba, and REE. Variations in Fe²⁺ and Fe³⁺ between the three zones were observed. The elements Si, Al, Fe²⁺, Mg, Ba, Cr, F, Li, Ni, Zn, and REE decrease from the core of the ore block outwards, corresponding to an increase in S and Fe³⁺. Depletions in Si, Al, Fe²⁺, Mg, Ba, and Cr were caused by the dissolution of amesite. Most of the Al and Si in amesite were lost during the weathering, and minor retained to form kaolinite. Depletions in Li, Ni, and Zn resulted from changes in the depositional environment between the late Permian and Quaternary. Dissolution of REE-bearing fluorocarbonates resulted in depletions of REE and F. The enrichment of Fe³⁺ and S was related to the precipitation of goethite, hematite, and barite in an oxidizing environment, while local enrichment of Ce resulted from the redox change of Ce³⁺ → Ce⁴⁺ under the same condition. This shows that the chemical composition of laterite enwrapping the bauxite also took part in Quaternary bauxite transformation. This study shows that the elements migrations during bauxite transformation were influenced by multiple independent factors except for the elemental attributes.     

Minéralogie et bilan de matière de l''altération supergène d''un basalte alcalin du Moyen Atlas Marocain

In the Middle Atlas of Morocco, alkali basaltic flows record successive weathering phases during the Quaternary. In fresh basalt interior and intermediate external zones, the first weathering stage is characterised by glass dissolution and the formation of a Si-Al poorly-crystallised product. Advanced weathering phases are characterised by 10 Å halloysite, kaolinite and goethite, located within the primary minerals or as secondary products in fissures. Olivine and iddingsite are transformed into Si-rich goethite, plagioclase into halloysite and pyroxene into a mixture of halloysite + geothite. Dissolution of Ti-magnetite and ilmenite yielded Ti-rich products. In these conditions, the weathering of basalts and development of a soil matrix are accompanied by the elimination of certain chemical elements, such as Si, Ca, Na and K, and the concentration of Fe and Al. In the soil, clay minerals such as illite and vermiculite, do not have any genetic relationship with weathered basalt and were probably introduced externally.     

Rock weathering by indigenous heterotrophic bacteria of Bacillus spp. at different temperature: a laboratory experiment

The bio-weathering of basalt, granite and gneiss was experimentally investigated in this study. These rock-forming minerals weathered more rapidly via the ubiquitous psychrotrophic heterotrophic bacteria. With indigenous bacteria of Bacillus spp. from sediments of Lake Baikal, we traced the degradation process of silicate minerals to understand the weathering processes occurring at the change temperature in the subsurface environment with organic input. The bacteria mediated dissolution of minerals was monitored with solution and solid chemistry, X-ray analyses as well as microscopic techniques. We determined the impact of the bacteria on the mineral surface and leaching of K, Ca, Mg, Si, Fe, and Al from silicate minerals. In the samples the release of major structural elements of silicates was used as an overall indicator of silicate mineral degradation at 4°C and 18°C from five medium exchanges over 255?days of rock bioleaching. The increase of temperature importantly affected the efficiency of Fe extraction from granite and basalt as well as Si extraction from granite and gneiss. In comparison with elemental extraction order at 4°C, Ca was substituted first by Fe or Si. It is evident that temperature influences rock microbial weathering and results in a change of elements extraction.     

贵州省凯里市大田铝土矿矿床地质特征及成矿规律分析

凯里市大田铝土矿是贵州省重要铝土矿成矿带凯里─黄平矿集区(带)内的重要矿床。通过工作发现:①二叠系梁山组是其含矿层位,矿体呈似层状、透镜状/漏斗状产出,总体走向NE,平均厚2.59 m,w(Al₂O₃)平均值为64.25%,铝硅比平均为5.25,铝土矿(332+333)矿石资源量978.38×10⁴ t;②矿石矿物以一水硬铝石为主,矿石结构一般为自形、半自形或它形粒状结构,构造主要为块状构造、孔隙状构造、层纹状构造,矿石类型以低硫低铁铝土矿为主;③矿床受断裂构造影响较大,在该区西北部的泥质岩相带中铝土矿成矿较好,矿体厚度与含矿岩系厚度成正比,矿石的w(Al₂O₃)值与w(SiO₂)值成反比;④高坡场组古岩溶洼地、槽沟是该区铝土矿找矿的有利部位。     

Comparison of Fused Glass Beads and Pressed Powder Pellets for the Quantitative Measurement of Al,Fe, Si and Ti in Bauxite by Laser‐Induced Breakdown Spectroscopy

Due to matrix interference and sample particle size effects, some of the most important and difficult issues in laser‐induced breakdown spectroscopy (LIBS) analysis are the calibration and quantitative measurement of a complex matrix. This study proposes the use of borate fusion as an alternative sample preparation procedure for the quantitative measurement of Al, Fe, Si and Ti in bauxite by LIBS. Analytical calibration curves were made using bauxite certified reference materials (CRM), and the precision and accuracy of the methods were evaluated by analysing an additional bauxite CRM, using two different approaches: pressed powder pellets and fused glass beads. The borate fusion method was the most suitable sample preparation technique, since particle size effects and matrix interference could be minimised, obtaining better linearity on the analytical calibration curves (r²), and more accurate and more precise results for bauxite analysis.     

Investigation of bauxites with the help of electron-probe

Summary 25 representative karstic and lateritic bauxite samples from Europe, Asia and Africa were studied by a JEOL-JXA-5 electron-probe X-ray microanalyser. The main directions of the investigation were: determination of the microtextures and the distribution of the main elements in bauxite (Al, Fe, Ti, Si). Conclusions on the genesis of the textural constitution and on bauxitization are given. Further possibilities of using the electron-probe in solving different problems connected with bauxites are enumerated.

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Bauxit-Untersuchungen mit der Elektronstrahl-Mikrosonde

Zusammenfassung Es wurden 25 typische Karst- und Lateritbauxite aus Europa, Asien und Afrika mit Hilfe einer JEOL-JXA-5 Elektronstrahl-Mikrosonde untersucht. Die Hauptrichtungen der Untersuchung waren die Bestimmung der Mikrostruktur und die Verteilung der Hauptelemente in den Bauxiten (Al, Fe, Ti, Si). Es wurden mehrere Schlüsse bezüglich der Entwicklung der Strukturelemente und der Bauxitbildung gezogen. Weitere Anwendungs-möglichkeiten zur Lösung verschiedener Bauxit-Probleme werden angegeben.

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With 30 Figures     

Metallogenic Model of Bauxite in Central Guizhou Province: an Example of Lindai Deposit

The bauxites in central Guizhou are hosted by the Lower Carboniferous Jiujialu Formation.Geochemistrial characteristics of the Lindai bauxite deposit indicate that the underlying Shilengshui Formation dolomite is the precursor rock of mineral resources.Weathering simulation experiments show that Si is most likely to migrate with groundwater,the migration rate of which is several magnitude higher than Al and Fe under nature conditions （pH=3-9）.The neutral and acid nonreducing condition is the most conducive to the Al rich and Si removal,while the acid reducing conditions is the most conducive to the Al rich and Fe removal.In the process of bauxite formation,coal beds overlying the Al-bearing rock series or other rock formation rich in organic materials can produce acid reducing groundwater,which are important for the bauxite formation.Finally,propose the metallogenic model of the bauxite in central Guizhou Province and put forward three new words which are ＂original bauxite material＂,＂bauxite material＂ and ＂original bauxite＂.     

Dissolution of well and poorly ordered kaolinites by an aerobic bacterium

Previous research by our group (e.g., [Chem. Geol. 132 (1996) 25; Geochim. Cosmochim. Acta 64 (2000) 1363]) has shown that an aerobic Pseudomonas mendocina bacterium enhances Fe(hydr)oxide dissolution in order to obtain Fe under Fe-limited conditions. The P. mendocina is incapable of utilizing Fe as a terminal electron acceptor and requires several orders of magnitude lower Fe concentrations than do dissimilatory Fe reducing bacteria. The research reported here compared the effects of the P. mendocina on dissolution of well and poorly ordered Clay Minerals Society Source Clay kaolinites KGa-1b and KGa-2, respectively, under Fe-limited conditions. KGa-1b and KGa-2 contain 0.04 and 0.94 bulk wt.% Fe, respectively, and their surface Fe/Si atomic RATIOS=0.008 and 0.012. Following strong cleaning of the kaolinites in 5.8 M HCl at 85 °C, the surface Fe/Si atomic ratios decreased to 0.004 and 0.008, respectively. Both kaolinites also developed a Si-enriched surface precipitate upon strong cleaning.

Because the P. mendocina take up Fe, we could not measure Fe release from the kaolinite directly, but rather had to monitor it indirectly by comparing microbial populations sizes under Fe-limited growth conditions. We found that microbial growth on uncleaned, weakly cleaned, and strongly cleaned kaolinites increased with the amount of Fe readily available to organic ligands as estimated by dissolution in 0.001 M oxalate (pH 3). This suggests that it is the amount of readily accessible Fe that controls Fe acquisition and hence microbial growth. The trend is based on only a relatively small range of kaolinite Fe contents, and the research thus needs to be expanded to include kaolinites with a broader range of bulk and surface Fe concentrations.

Significant enhancement of Al release was observed in the presence of the bacteria, along with generally some enhancement of Si release. This enhancement of kaolinite dissolution could be related to an observed pH increase from 7–8 to 9 in the presence of the bacteria and/or to production of Al chelating agents. The P. mendocina produce a variety of organic exudates, including siderophores [Chem. Geol. 132 (1996) 25; Geomicrobiology (2001b)], and further studies into the effects of the siderophores on Al complexation and on kaolinite dissolution are ongoing.     

Geochemistry, mineralogy and genesis of pyrophyllite deposits in the Pötürge Region (Malatya, Eastern Turkey)

In the Pötürge (Malatya, Turkey) area pyrophyllite occurrences are common in the shear zones, mostly in the form of lenses along faults. Mineralogical investigations (XRD, FTIR and SEM) revealed that pyrophyllite, kaolinite (dickite) and quartz are present in the form of major phases and muscovite (sericite), kyanite, chlorite, and alunite are only present in the form of minor phases. This study revealed that the existence of the kyanite phase points out to high pressure and temperature conditions which the rocks were underwent. On the other hand, the minerals such as pyrophyllite, kaolinite, and alunite are products of a low degree metamorphism (retrograde). The mineral paragenesis in the pyrophyllite deposits suggests that the formation of minerals took place in two ways: (1) the transformation of kyanite into pyrophyllite and quartz through retrograde metamorphism by a high degree temperature, (2) then pyrophyllite and probably muscovite were transformed into kaolinite and alunite through reactions with relatively low temperature hydrothermal fluids. The geochemical data indicate that during the retrograde metamorphism the elements K, Rb, Sr, Ba, S, and Fe were mobile, the elements Si, Al, P moderately mobile to immobile and the HPS elements (Zr, Ti, and Nb) were immobile. It was shown that the formation of pyrophyllite, kaolinite and alunite was associated with depletion in alkalis, Mg, Fe and enrichment of elements including Sr, Ba, and S. Mineralogical and geochemical data suggest that parent rocks (pre-metamorphism) of the Pötürge pyrophyllite were probably kaolinite, Al-rich clays or bauxites.     

大庆油田三元复合驱液与储层矿物反应性研究

三元复合驱技术能够显著提高石油的采收率,但在生产过程中三元复合注入液易与储层矿物反应,破坏储层并结垢,造成井下堵塞、采收率降低等问题,因此研究三元复合驱液在储层中的溶、运、堵过程及反应机理成为当务之急。本文利用X射线衍射(XRD)、X射线光电子能谱(XPS)、场发射环境扫描电镜(ESEM)及X射线能谱仪(EDS)测试手段精细表征了大庆油田储层矿物钾长石、石英、高岭石与强碱三元复合驱液作用的反应过程及变化特征,并通过反应动力学计算得到了相应的Si、Al溶出动力学方程及矿物溶蚀再沉积规律,深入探讨了反应机理。结果显示,钾长石与强碱复合驱液作用60 d后Si溶出量约为Al的3倍,生成三水铝石和硅酸盐沉淀物;石英的Si溶出量呈线性增加,60 d后超过300×10-6,表面生成碳酸盐颗粒;高岭石60 d后Al溶出量约为Si的3倍,结晶度下降25.26%,生成水钙沸石;强碱对矿物的溶蚀破坏程度与其浓度呈正相关。     

Fe-solid phase transformations under highly basic conditions

Hyperalkaline and saline radioactive waste fluids with elevated temperatures from S-SX high-level waste tank farm at Hanford, WA, USA accidentally leaked into sediments beneath the tanks, initiating a series of geochemical processes and reactions whose significance and extent was unknown. Among the most important processes was the dissolution of soil minerals and precipitation of stable secondary phases. The objective of this investigation was to study the release of Fe into the aqueous phase upon dissolution of Fe-bearing soil minerals, and the subsequent formation of Fe-rich precipitates. Batch reactors were used to conduct experiments at 50 °C using solutions similar in composition to the waste fluids. Results clearly showed that, similarly to Si and Al, Fe was released from the dissolution of soil minerals (most likely phyllosilicates such as biotite, smectite and chlorite). The extent of Fe release increased with base concentration and decreased with Al concentration in the contacting solution. The maximum apparent rate of Fe release (0.566 × 10⁻¹³ mol m⁻² s⁻¹) was measured in the treatment with no Al and a concentration of 4.32 mol L⁻¹ NaOH in the contact solution. Results from electron microscopy indicated that while Si and Al precipitated together to form feldspathoids in the groups of cancrinite and/or sodalite, Fe precipitation followed a different pathway leading to the formation of hematite and goethite. The newly formed Fe oxy-hydroxides may increase the sorption capacity of the sediments, promote surface mediated reactions such as precipitation and heterogeneous redox reactions, and affect the phase distribution of contaminants and radionuclides.     

Mobilization of aluminium and magnesium by roots of banana (Musa spp.) from kaolinite and smectite clay minerals

Banana plants (Musa spp.) are very sensitive to Al, which is mobilized in acid soil conditions. These plants may, however, contribute to their own intoxication because their roots can excrete protons in large quantities. The authors studied the mobilization of Al by banana roots from clay minerals in experimental designs exacerbating the root–mineral contact. The plants were grown on agarose-gel or sand substrates previously mixed with smectite (montmorillonite) and kaolinite as sole source of Al. The pH and the ion concentrations in the aqueous and exchangeable phases of the substrates were determined as concentrations of Al, Ca, Mg and K in plants. In both agarose and sand substrates, pH significantly decreased in the close vicinity of roots, relative to the bulk substrate. This root-induced acidification involved a preferential mobilization of Al in kaolinite substrates and of Mg in smectite substrates, and thereby a significant plant uptake of Al and Mg from these respective substrates. Root-induced weathering of kaolinite and montmorillonite thus suggests that the mobilization of, respectively, Al and Mg are the limiting steps in the dissolution of these respective minerals, just as demonstrated in previous chemical weathering studies.     

Combination of multi-scale and multi-edge X-ray spectroscopy for investigating the products obtained from the interaction between kaolinite and metallic iron in anoxic conditions at 90 °C

In the context of radioactive waste repository in geological formation, kaolinite-metallic iron interaction in chlorine solution was conducted in batch experiments, under anoxic conditions at 90 °C during 9 months. After a mineralogical characterization at a global scale, products were analyzed at the micrometer and nanometer scales by X-ray absorption spectroscopic techniques (XAS and STXM). Absorption at Al, Si and Fe edges was investigated to have a complete overview of the distribution and status of constituting elements. Whereas Si K-edge results do not evidence significant evolution of silicon status, investigations at Al K-edge and Fe L-edges demonstrate variations at aggregate and particle scales of ^IVAl:^VIAl and Fe²⁺:Fe³⁺ ratios. Spectroscopic data evidence the systematic crystallization of Fe-serpentines onto the remaining particles of kaolinite and the absence of pure species (kaolinite or Fe-serpentines). Combination of spatially resolved spectroscopic analyses and TEM-EDXS elemental distribution aims to calculate unit cell formulae of Fe-serpentines layers and abundance of each species in mixed particles. For most of the investigated particles, results reveal that the variations of particles composition are directly linked to the relative contributions of kaolinite and Fe-berthierine in mixed particles. However, for some particles, microscale investigations evidence crystallization of two other Fe-serpentines species, devoid of aluminum, cronstedtite and greenalite.     

河南省偃龙煤田深部铝土矿床地质特征

偃龙煤田深部铝土矿矿床是豫西典型的隐伏铝土矿床,赋存于中奥陶统侵蚀面之上的石炭系本溪组中.含矿岩系的厚度及矿体形态受古岩溶面控制,构造对矿体影响较大.矿石主要矿物成分为一水硬铝石、高岭石、伊利石等含铝矿物.上部铝质泥岩以高岭石为主,下部铝质泥岩以伊利石为主.铝土矿共生矿产综合开发价值大,伴生矿产有待进一步研究.     

Weathering of the zinc-lead lode, Dugald River, northwest Queensland: I. the gossan profile

Oxidation of the relatively iron sulfide-poor Dugald River zinc-lead lode in northwest Queensland and reaction of the acid solutions with carbonate has resulted in an undifferentiated gossan profile. The gossan is composed predominantly of quartz, goethite, hematite, barite, adularia, plumbian jarosite, plumbogummite and minor mica, chlorite, kaolinite and montmorillonite. Barite and adularia are formed by the breakdown of the barium feldspar hyalophane (K, Na, Ba)[(Al, Si)₄O₈] which occurs in the lode.Lead in the gossan is contained within the secondary minerals plumbogummite and plumbian jarosite, and in traces of anglesite and cerussite, whereas Zn occurs in the barite, secondary lead minerals and coronadite structures, and is adsorbed by iron oxides, phyllosilicates and carbonaceous matter. Only traces of zinc minerals smithsonite, goslarite and hemimorphite were detected.Use of Gresens' general metasomatic equation has enabled quantitative determination of compositional changes resulting from the oxidation of the ore. Silicon, Al, Ti and Ba are essentially immobile under the mildly acidic oxidizing conditions. In decreasing order of mobility Cd, Ca, S, Na, K, Mn, Mg, Zn, Ni and Cu, together with CO₂ and Tl, have been leached from the gossan profile, while Ag, Sb, Se, As, Fe and Pb appear to have been added to the gossan, notably in a zone of solution-deposited secondary minerals where they have been concentrated, possibly as a result of leaching from the surface gossan.