Mechanism of pyroxene and amphibole weathering—I. Experimental studies of iron-free minerals

The short term (2–40 days) dissolution of enstatite, diopside, and tremolite in aqueous solution at low temperatures (20–60°C) and pH 1–6 has been studied in the laboratory by means of chemical analyses of reacting solutions for Ca²⁺, Mg²⁺, and Si(OH)₄ and by the use of X-ray photoelectron spectroscopy (XPS) for detecting changes in surface chemistry of the minerals. All three minerals were found to release silica at a constant rate (linear kinetics) providing that ultrafine particles, produced by grinding, were removed initially by HF treatment. All three also underwent incongruent dissolution with preferential release of Ca and/or Mg relative to Si from their outermost surfaces. The preferential release of Ca, but not Mg for diopside at pH 6 was found by both XPS and solution chemistry verifying the theoretical prediction of greater mobility of cations located in M₂ structural sites. Loss mainly from M₂ sites also explains the degree of preferential loss of Mg from enstatite at pH 6; similar structural arguments apply to the loss of Ca and Mg from the surface of tremolite. In the case of diopside and tremolite initial incongruency was followed by essentially congruent cation-plus-silica dissolution indicating rapid formation of a constant-thickness, cation-depleted surface layer. Cation depletion at elevated temperature and low pH (~ 1) for enstatite and diopside was much greater than at low temperature and neutral pH, and continued reaction resulted in the formation of a surface precipitate of pure silica as indicated by solubility calculations, XPS analyses, and scanning electron microscopy.From XPS results at pH 6, model calculations indicate a cation-depleted altered surface layer of only a few atoms thickness in all three minerals. Also, lack of shifts in XPS peak energies for Si, Ca, and Mg, along with undersaturation of solutions with respect to all known Mg and Ca silicate minerals, suggest that cation depletion results from the substitution of hydrogen ion for Ca²⁺ and/or Mg²⁺ in a modified silicate structure and not from the precipitation of a new, radically different surface phase. These results, combined with findings of high activation energies for dissolution, a non-linear dependence on a_H⁺ for silica release from enstatite and diopside, and the occurrence of etch pitting, all point to surface chemical reaction and not bulk diffusion (either in solution or through altered surface layers) as the rate controlling mechanism of iron-free pyroxene and amphibole dissolution at earth surface temperatures.     

Heavy Mineral Placer Sand Deposits of Kontiagarh Area,Ganjam District,Orissa, India

The Kontiagarh placer deposit in the Ganjam district, Orissa, India extends in northeast direction having a width of 700–1000 m. A total of 187 samples were collected meterwise from 55 bore holes in a grid pattern from beach, frontal, intermediate and back dunes covering an area of approximately 1 km². Light minerals decrease in size from the beach to the back dunes, whereas the size distribution of heavy minerals in the beach and dunes is more or less uniform. The average heavy mineral content in the beach and dunes vary from 9.38% to 24.20%. The heavy minerals are ilmenite, garnet, sillimanite, rutile, monazite, and zircon with trace amounts of magnetite, hornblende, diopside, sphene, tourmaline, and epidote. Heavy minerals are mostly less than 350 µm in size, with a peak distribution in the range between 180 and 125 µm. Ilmenite shows exsolution intergrowth with hematite. Mineral chemistry of ilmenite, hematite, leucoxene, magnetite, monazite and sillimanite are examined by EPMA. Leucoxene is lower in Fe and higher in Ti, Al, Cr and V than ilmenite. The litho‐units of the Precambrian Eastern Ghats Mobile Belt, comprising primarily khondalite, charnockite, calc‐silicate granulite and gneiss, are the source of heavy minerals for this deposit. The bulk sample has 7.30% ilmenite, 5.24% sillimanite, 9.16% garnet, 0.18% rutile, 0.14% monazite, 0.06% zircon and 0.52% other heavy minerals. The deposit has good potential for economic exploitation of ilmenite, rutile, sillimanite, monazite, zircon and garnet.     

焦家金矿选厂旋流器溢流产品工艺矿物学分析

焦家金矿选矿厂目前的日处理量达12000吨/天,金回收率92%。选矿厂已将破碎段产品用双螺旋分级机洗矿,洗矿的矿泥产率为7%,矿泥单独浮选,整体工艺初步实现了泥砂分选。为进一步提高选金回收率,流程改造拟将磨矿-浮选系统的旋流器溢流产品二次分级,分级的次生矿泥与洗矿矿泥进入矿泥浮选系统一并浮选,为了掌握旋流器溢流产品的性质,本文采用偏光反光两用显微镜、扫描电镜、X射线衍射仪、红外光谱和差热分析等手段进行研究。研究结果表明矿物种类主要是金属硫化物和脉石矿物,金属硫化物约占4%,脉石约占96%,金属硫化物主要是黄铁矿(70.17%)和黄铜矿(16.27%),脉石主要是石英(47.12%)和长石(15.90%)。黄铁矿和石英是重要的载金矿物,黄铁矿含金65%,石英含金20%。颗粒越细,单体颗粒含量越高,连生体颗粒含量越少;颗粒越细,黄铁矿含量越高,Au、Ag分布率越高,-0.037 mm粒级中黄铁矿含量达到73.58%,Au、Ag占到47.99%和56.60%,金分配率与黄铁矿含量成正相关;粗粒级中未发现金颗粒,中等粒级中次显微金约占30%,细粒级中次显微金约40%,金粒径在2~10μm范围内;金形状有三角形、棱角状、小粒状、不规则状等。红外光谱与差热曲线研究发现颗粒越细矿物成分趋于复杂。研究结论为磨矿分级产生的次生矿泥浮选调控提供了依据,对矿泥浮选的药剂制度调控、浮选流程确定等具有重要实际意义。     

铜铅锌混合精矿的矿物学特征分析及分离效率探究

中国云南省有大量的铜铅锌多金属硫化矿资源,该类矿产资源的高效选矿分离是影响企业经济效益的主要问题之一.针对云南迪庆地区的硫化混合精矿,该混合精矿铜、铅、锌三种有价金属共存,分离难度较大,导致其产品难以销售或冶炼.本文采用化学分析、X射线衍射法和矿物解离度分析(MLA)等多种检测方法,对该混合精矿的主要元素含量、矿物组成...     

FEG-EPMA mapping and Fe-Ti oxide mineral chemistry of Brahmaputra River sediments in Bangladesh: provenance and petrogenetic implications

The present research deals with the FEG-EPMA mapping and Fe-Ti oxide mineral chemistry of Brahmaputra River sediments in Bangladesh. Major heavy minerals in the sediments consist of garnet (8.5–21.3%), kyanite (5.35–11.9%), monazite (2.3–5.3%), sillimanite (1.8–4.7%), zircon (3.6–9.1%), and a considerable amount of opaques mainly Fe-Ti oxide minerals (23.1–35.4%). The detrital Fe-Ti oxide minerals carry significant clues to the parent rocks or sources. In these contexts, detrital opaques (Fe-Ti oxides) have been analyzed with an electron probe microanalyzer (EPMA). These opaques (Fe-Ti oxide) display six types of textural patterns, dominantly seriate with granular, emulsion, and acicular sandwich structures and trellis type of textural patterns. These textural patterns belong to five intergrowths of Fe-Ti oxide minerals such as (1) ilmenite-hematite, (2) magnetite-ilmenite, (3) hematite-rutile, (4) ilmenite-hematite-rutile, and (5) ilmenite-rutile, where ilmenite-hematite intergrowth is common. Alteration is seen in both exsolved and unexsolved ilmenites. Textural patterns and mineral chemistry of the studied ilmenite minerals provide lines of evidence of low-temperature magmatic inheritance, later modified by diffusional processes. The estimated temperature and oxygen fugacity from the magnetite-ilmenite exsolution range from 547.6 to 558.2 °C and from 10^?21.4 to 10^?21.7, respectively. The data are also consistent with hematite-ilmenite temperature (between 537 and 540 °C) and oxygen fugacity (10^?21.7 to 10^?21.9) measurements in Cox’s Bazar beach placers. These temperatures and oxygen fugacities specify Fe-Ti oxide assemblages equilibrated in a T-fO₂ field very near to the FMQ buffer curve suggesting a crustal source (magmatic and/or metamorphic), which is modified significantly by metamorphic processes.     

Experimental modeling of the immobilization of heavy metals at the carbonate adsorption–precipitation geochemical barrier

Experimental data obtained on the adsorption–precipitation immobilization of heavy metals (Cu, Zn, Pb, Cd, Co, and Ni) from acidic and neutral solutions by calcite and dolomite demonstrate that interaction of solutions of heavy metals with these minerals at pH > 7.8–8.1 leads to a significant decrease in the concentrations of the metals because of the crystallization of carbonates of these metals. Except Pb, which is equally removed from solutions by both minerals, the immobilization efficiency of the metals on dolomite is greater than on calculate at the same pH. Residual Zn, Cd, Co, and Ni concentrations are immobilized by chemosorption, which is the most efficient for Cd and less significant for Co, Ni, and Zn. It is proved that artificial geochemical barriers on the basis of carbonate rocks can be efficiently applied to protect environment from contamination with heavy metals.     

Uranium-rich opal from the Nopal I uranium deposit, Peña Blanca, Mexico: Evidence for the uptake and retardation of radionuclides

The Nopal I uranium deposit of the Sierra Peña Blanca, Mexico, has been the focus of numerous studies because of its economic importance and its use as a natural analog for nuclear-waste disposal in volcanic tuff. Secondary uranyl minerals such as uranophane, Ca[(UO₂)(SiO₃OH)]₂(H₂O)₅, and weeksite, (K,Na)₂[(UO₂)₂(Si₅O₁₃)](H₂O)₃, occur in the vadose zone of the deposit and are overgrown by silica glaze. These glazes consist mainly of opal A, which contains small particles of uraninite, UO₂, and weeksite. Close to a fault between brecciated volcanic rocks and welded tuff, a greenish silica glaze coats the altered breccia. Yellow silica glazes from the center of the breccia pipe and from the high-grade pile coat uranyl-silicates, predominantly uranophane and weeksite. All silica glazes are strongly zoned with respect to U and Ca, and the distribution of these elements indicates curved features and spherical particles inside the coatings. The concentrations of U and Ca correlate in the different zones and both elements inversely correlate with the concentration of Si. Zones within the silica glazes contain U and Ca in a 1:1 ratio with maximum concentrations of 0.08 and 0.15 at.% for the greenish and yellow glazes, respectively, suggesting trapping of either Ca₁U₁-aqueous species or -particles in the colloidal silica. X-ray photoelectron spectroscopy (XPS), Fourier-transform infra-red spectroscopy (FTIR), and oxygen-isotope ratios measured by secondary-ion mass spectrometry (SIMS) indicate higher U⁶⁺/U⁴⁺ ratios, higher proportions of Si-OH groups and lower δ¹⁸O values for the greenish silica glaze than for the yellow silica glaze. These differences in composition reflect increasing brecciation, porosity, and permeability from the center of the breccia pipe (yellow silica glaze) toward the fault (green silica glaze), where the seepage of meteoric water and Eh are higher.     

Heavy metal adsorption by sulphide mineral surfaces

The adsorption of aqueous Hg²⁺, Pb²⁺, Zn²⁺ and Cd²⁺ complexes on a variety of sulphide minerals has been studied as a function of the solution pH and also as a function of the nature of the ligands in solution. Sulphide minerals are excellent scavengers for these heavy metals. The adsorption is strongly pH dependent, i.e. there is a critical pH at which the adsorption increases dramatically. The pH dependence is related to the hydrolysis of the metal ions. Indirect evidence suggests that the hydrolyzed species are adsorbed directly on the sulphide groups, probably as a monolayer. The results also suggest the presence of MCI_n²⁻ⁿ species physisorbed on the adsorbed monolayer. A positive identification of the adsorbed species was not possible using ESCA/XPS.     

Geological analogue for circumneutral pH mine tailings: implications for long-term storage,Macraes Mine,Otago, New Zealand

Tailings from the Macraes Au mine cyanidation process are stored in an impoundment about 0.6 km² and 80 m deep whose pH is maintained near 8 by the neutralizing capacity of the gangue minerals. The tailings are sandy (>50 μm particles), have a hydraulic conductivity of about 10⁻² m/day, and contain 0.1–1.0 wt.% S and 0.1–1.5 wt.% graphitic C from the primary deposit. Concentrations of As in the pore water of the mixed tailings, which are a combination of various tailings types, range from 0.1 to 20 ppm, HCO₃^- is 100 to 200 ppm, and dissolved SO₄ is 100–1700 ppm. The mixed tailings will be stored in this impoundment in perpetuity after mining ceases. Confidence in the long-term pH stability of these tailings can be gained from examination of mineralogically and chemically similar geological analogues in the immediate vicinity. A sequence, typically about 5 m thick, of sands and gravels derived from the Macraes mineralized zone 12–28 ka ago contains rounded detrital sulfide mineral grains which are unoxidized despite their close proximity to the surface and the occasional incursion of oxygenated waters. These sediments have a hydraulic conductivity of about 10⁻⁴ m/day. Saturating water pH is currently 7–8. Sands with 0.2–0.8 wt.% organic C host SO₄-reducing bacteria (SRB), and local cementation by authigenic framboidal pyrite has occurred. SRB were found in water-saturated sediments with decreased hydraulic conductivity and alkaline and anoxic conditions. These bacteria are involved in the formation of authigenic framboidal pyrite, reducing the cycling of dissolved Fe in the sediments. Carbon is not a limiting factor in this process as organic matter is present in the sandstone and ground water contains up to 180 ppm HCO₃^-. Comparison of the 28 ka old sediments with the modern tailings suggests that the chemical behaviour of the two will be similar, possibly with the crystallization of authigenic pyrite in the tailings over the long term. As long as the present slightly anoxic and circumneutral pH environmental conditions are maintained in the mixed tailings impoundment, sulfide decomposition and acidification are unlikely.     

Joint clay–heavy–light mineral analysis: a tool to investigate the hydrographic–hydraulic regime of Late Cenozoic deltaic inland fans under changing climatic conditions (Cuvelai-Etosha Basin, Namibia)

An interdisciplinary study (major and minor elements, C and O isotopes, heavy and light minerals, phyllosilicates, wireline logs) in northern Namibia unraveled the hydrographic and hydraulic evolution of alluvial–fluvial sediments of the Kunene and Cubango megafans (Etosha-Cuvelai Basin). Three principal aquatic regimes were operative within the megafan complex: (1) the hydrographic regime, (2) the proximal hydraulic regime, (3) the distal hydraulic regime. The allogenic mineral assemblages mirror the hydrographic variation or drainage system and the lithological evolution of the fan sediments (alluvial–fluvial fan, lacustrine environment with evaporites, fan delta progradation). Authigenic heavy minerals are markers of the physical–chemical condition (Eh and pH values) of the hydraulic regime within the proximal fan at the basin margin. Authigenic heavy, light and clay minerals equally contribute to the determination of the fluid chemistry and temperature, as well as the source of chemical constituents of the former pore fluids percolating through the distal fan. Carbonatization was the most pronounced event in the distal hydraulic system and controlled by the presence of biogenic as well as atmospheric carbon. The isotope-based determination of the temperatures, albeit strongly fluctuating, do not exceed 40 °C. The overall pH values determined for the hydraulic regime within the distal fan range from slightly acidic to alkaline. The presence of zeolites attests to some short-lasting but strong deviations from the pH range, mainly towards more alkaline conditions. Heavy, light and clay mineral analyses proved to be a useful tool to determine the (paleo)hydrology of alluvial–fluvial fan systems in tropical arid to semiarid climates.     

Experimental study of the selective adsorption of heavy metals onto clay minerals

The interaction between minerals and heavy metals has been a hot object of study in environmental science,mineralogy and soil science,Through the selective adsorption experiment of Ca-montomorillonite,illite and kaolinite to Cu2 ,Pb^2 ,Zn^2 ,Cd^2 ,and Cr^3 ions at certain conditions,it could be concluded that Cr^3 is most effectively sorbed by all the three minerals.Also,it can be found that Pb^2 shows a strong affinity for illite and kaolinite while cu^2 for montmorillonite .Based on the adsorption experiment at varying pH of solution,it can be found that the amount of heavy etals sorbed by minerals increases with increasing pH of the solution.     

Uranyl Retention on Quartz—New Experimental Data and Blind Prediction Using an Existing Surface Complexation Model

The adsorption behaviour of uranyl onto seven different samples of quartz was studied in batch experiments. Sea-sand (0.1–0.3 mm), Fil-Pro 12/20 (1–2 mm) and five Min-U-Sil samples with smaller particle sizes (5, 10, 15, 30 and 40 μm) were used. The uptake curves show “pH adsorption edges” in the range of pH 4–5. A good agreement of the new data with literature data was found when plotting surface-normalised distribution coefficients versus pH. Differences in the adsorption behaviour for pre-treated and untreated sea-sand samples were detectable resulting in a shift of the pH edge to higher pH values after treatment. A literature surface complexation model was applied for blind predictions of the experimental results. The simulations described the experimental observations quite well for the Min-U-Sil samples. For the two coarser quartz samples, the calculated over-predictions were explained by the larger-than-expected measured specific surface area and measurable amounts of associated minerals, for Fil-Pro 12/20 and sea-sand, respectively. Dissolution of the samples was studied as a function of pH. After 5 days, the measured Si concentrations were all higher than equilibrium quartz solubilities, but lower than those of amorphous silica. With increasing pH, dissolved silica increased. This strongly suggests that formation of dissolved uranyl–silicato complexes have to be considered based on measured silica concentrations.     

Effect of collector, pH and ionic strength on the cationic flotation of kaolinite

The effect of amine collector type, pH, and ionic strength on the flotation behaviour of kaolinite was investigated in a series of laboratory batch flotation tests. In distilled water, ether diamine, a strong collector for silica, does not induce any flotation or only very weak flotation of kaolinite over a wide pH range from pH 3 to pH 10.5. Ether monoamine causes strong flotation of kaolinite in distilled water, especially in acidic solutions, but high dosages of the collector are required. Such observations are in contrast to the flotation behaviour of oxide minerals such as silica for which ether diamine shows stronger collecting power than ether monoamine. The pH dependence of kaolinite flotation is also opposite to that of oxides, with lower flotation recovery obtained at higher pH. In contrast to oxides, the flotation recovery of kaolinite increases with ionic strength. It was demonstrated that the enhanced flotation of kaolinite in NaCl solutions cannot be attributed to the frothing ability of NaCl or the intercalation of kaolinite by alkylamines. It is proposed that the screened zeta potential of kaolinite particles in a high ionic strength environment causes random aggregation of kaolinite particles exposing hydrophobic (001) silica plane in the presence of ether amines.     

Transformational changes of clay minerals, zeolites and silica minerals during diagenesis

Diagenetic transformation of clay minerals, zeolites and silica minerals in Cretaceous and Tertiary argillaceous rocks from deeply drilled wells in Japan were studied. Transformations of these minerals during diagenesis were as follows: in clay minerals, montmorillonite → montmorillonite-illite mixed-layer mineral → illite; in zeolites, volcanic glass → clinoptilolite → heulandite and/or analcite → laumontite and/or albite; in silica minerals, amorphous silica → low-cristobalite → low-quartz. Maximum overburden pressures and geothermal temperatures corresponding to these transformations in each well studied were calculated. For clay minerals, a pressure of approximately 900 kg cm^?2 and a temperature of about 100°C are necessary for the transformation from montmorillonite to mixed-layer mineral and 920 kg cm^?2 and 140°C for mixed-layer mineral to illite. Transformation from kaolinite to other minerals requires much higher pressures and temperatures than from montmorillonite to mixed-layer mineral. For zeolites, 330 kg cm^?2 and 60°C are required for the transformation from volcanic glass to clinoptilolite, 860 kg cm^?2 and 120°C for clinoptilolite to heulandite and/or analcite, and 930 kg cm^?2 and 140°C for heulandite and/or analcite to laumontite and/or albite. For silica minerals, 250 kg cm^?2 and 50°C are necessary for the transformation from amorphous silica to low-cristobalite and 660 kg cm^?2 and 70°C for low-cristobalite to low-quartz. Based on these diagenetic mineral transformations, seven mineral zones are recognized in argillaceous sediments. On the other hand, from the porosity studies of argillaceous sediments in Japan, the process of diagenesis is classified into the following three stages. The early compaction stage is marked by shallow burial and viscous rocks with more than 30% porosity. The late compaction stage is characterized by intermediate burial and plastic rocks with 30-10% porosities. The transformation stage is marked by deep burial and elastic rocks with less than 10% porosity.     

Genesis and evaluation of heavy minerals in black sands: A case study from the southern Eastern Desert of Egypt

Black sands in the southern Eastern Desert (SED) of Egypt contain substantial reserves of heavy minerals (up to 5 %), and are found mainly in three basins namely: Hodein, Ibib and Diit between Shalateen and Halayeeb cities. The heavy minerals in these black sands include ilmenite-leucoxene (31 %–44 %), magnetite (15–18 %), zircon (11–21 %), garnet and green silicates (11–15 %), rutile (6–12 %) and monazite (2–4 %). Cassiterite, thorite, uranothorite, gold, xenotime and chromian spinel are minor quantities (<1 %). Magnetite (FeO: 75–93.5 wt%) and ilmenite (TiO₂: 42.7–56.9 wt%), hosting high Mn, V, Zr, Zn, Cr, Nb and Co, were probably derived from gabbroic rocks. The detrital chromian spinel composition (Cr#, 0.51–0.61; Mg#, 0.5–0.63; TiO₂ < 1.0 wt%) and its morphology are similar to those of spinels in fore-arc peridotites from the SED of Egypt, suggesting dominance of fore-arc basins for peridotite emplacement. These basins were formed during arc-arc or arc-oceanic crust collision and encolsed ophiolites, gabbroic rocks and I-type granites as sources of the SED black sands. The studied garnets are mostly almandine in composition with few grossularite and spessartine; they might have been derived from I-type granites and gneisses sources. The rutile and monazite show enriched LREE relative to HREE, and display marked defeciency in Eu, suggesting highly fractionated granitic rocks as a main source. Two distinct types of zircon are recorded: radioactive (Hf: 1578–8770, Y: 319–1335, U: 36–114 and Th: 40–64 ppm) and non radioactive (Hf: 427, Y: 44, U: 2 and Th: 2 ppm); they were probably derived from different granitic sources. Compositions and P-T conditions (T: 655–970 °C, P: 1.18–9.53 kbar) of magmatic amphiboles are similar to those derived from I-type granitoids. Bulk analyses of the economic heavy mineral assemblages show significant concentrations of Fe (393 kg/ton)_, Zr (183 kg/ton) and Ti (129 kg/ton) with minor Cr (14 kg/ton), Ba (7 kg/ton), Hf (4.9 kg/ton), Th (up to 3.34 kg/ton) and U (0.29 kg/ton). The elevated contents of Th and U could be related to the occurrence of monazite and zircon with subordinate thorite, uranothorite and xenotime. The total REE contents of these bulk analyses range from 1 to 4 kg/ton, where LREEs form 80–90 % of total REEs. Monazite (ΣREEs: 443604 ppm on average), garnet, zicon (ΣREEs: 421 ppm) and rutile (ΣREEs: 309 ppm) are the main host of REEs in the investigated black sands. Tonnages of raw sands, to a depth of one meter, are estimated per 10 km² in each basin, giving 18 million tons for Ibib basin and 19 million tons for both Diit and Hodein basins. Economic heavy minerals constitute 6–26 % of the total heavy minerals and around 1.0 % of total raw sands. Calculated reserves of these economic minerals, per 10 km² of black sands, range from 0.1 million ton in Ibib and Hodein basins to 0.2 million ton in the Diit basin.     

Heavy metal anomalies in the Tinto and Odiel River and estuary system,Spain

The Tinto and Odiel rivers drain 100 km from the Rio Tinto sulphide mining district, and join at a 20-km long estuary entering the Atlantic Ocean. A reconnaissance study of heavy metal anomalies in channel sand and overbank mud of the river and estuary by semi-quantitative emission dc-arc spectrographic analysis shows the following upstream to downstream ranges in ppm (μg g^?1): As 3,000 to <200, Cd 30 to <0.1, Cu 1,500 to 10, Pb 2,000 to <10, Sb 3000 to <150, and Zn 3,000 to <200. Organic-rich (1.3–2.6% total organic carbon, TOC), sandysilty overbank clay has been analyzed to represent suspended load materials. The high content of heavy metals in the overbank clay throughout the river and estuary systems indicates the importance of suspended sediment transport for dispersing heavy metals from natural erosion and anthropogenic mining activities of the sulfide deposit. The organic-poor (0.21–0.37% TOC) river bed sand has been analyzed to represent bedload transport of naturally-occurring sulfide minerals. The sand has high concentrations of metals upstream but these decrease an order of magnitude in the lower estuary. Although heavy metal contamination of estuary mouth beach sand has been diluted to background levels estuary mud exhibits increased contamination apparently related to finer grain size, higher organic carbon content, precipitation of river-borne dissolved solids, and input of anthropogenic heavy metals from industrial sources. The contaminated estuary mud disperses to the inner shelf mud belt and offshore suspended sediment, which exhibit metal anomalies from natural erosion and mining of upstream Rio Tinto sulphide lode sources (Pb, Cu, Zn) and industrial activities within the estuary (Fe, Cr, Ti). Because heavy metal contamination of Tinto-Odiel river sediment reaches or exceeds the highest levels encountered in other river sediments of Spain and Europe, a detailed analysis of metals in water and suspended sediment throughout the system, and epidemiological analysis of heavy metal effects in humans is appropriate.     

Characterization of the chemical structures of natural and synthetic aluminosilicate gels and sols by infrared spectroscopy

Infrared spectra in the 300–1400 cm^?1 region indicate that the non-crystalline products of interaction between hydroxyaluminium species and orthosilicic acid in dilute aqueous solutions of pH < 5 differ markedly in structure from those formed in near-neutral and alkaline solutions of pH > 6. The compound formed in acid solution has an infrared spectrum similar to imogolite, and is termed proto-imogolite; like imogolite, it contains orthosilicate groups and 6-coordinated aluminium, and has an ideal Si:Al ratio of around 0.5, but it can incorporate some excess alumina or silica and it does not have the regular tubular structure of imogolite. Compounds formed in alkaline solutions that are not too dilute have infrared spectra resembling the feldspathoid group of minerals and are termed hydrous feldspathoids. They incorporate a condensed tetrahedral framework with an Si:Al ratio greater than one, but can also contain 6-coordinated aluminium.Natural allophanes of the proto-imogolite and hydrous feldspathoid types exist. The allophane of weathered pumice, however, contains a condensed silicate anion that incorporates little tetrahedral aluminium. Proto-imogolite forms stable sols at pH < 5 and must play an important role in the transport of aluminium in acidic natural waters containing dissolved silica.     

Understanding heavy mineral enrichment using a three‐dimensional numerical model

Layered deposits of relatively light and heavy minerals can be found in many aquatic environments. Quantification of the physical processes which lead to the fine‐scale layering of these deposits is often limited with flumes or in situ field experiments. Therefore, the following research questions were addressed: (i) how can selective grain entrainment be numerically simulated and quantified; (ii) how does a mixed bed turn into a fully layered bed; and (iii) is there any relation between heavy mineral content and bed stability? Herein, a three‐dimensional numerical model was used as an alternative measure to study the fine‐scale process of density segregation during transport. The three‐dimensional model simulates particle transport in water by combining a turbulence‐resolving large eddy simulation with a discrete element model prescribing the motion of individual grains. The granular bed of 0·004 m in height consisted of 200 000 spherical particles (D50 = 500 μ m). Five suites of experiments were designed in which the concentration ratio of heavy (5000 kg m⁻³) to light particles (i.e. 2560 kg m⁻³) was increased from 6%, 15%, 35%, 60% to 80%. All beds were tested for 10 sec at a predefined flow speed of 0·3 m sec⁻¹. Analysis of the particle behaviour in the interior of the beds showed that the lighter particles segregated from the heavy particles with increasing time. The latter accumulated at the bottom of the domain, forming a layer, whereas the lighter particles were transported over the layer forming sweeps. Particles below the heavy particle layer indicated that the layer was able to armour the particles below. Consequentially, enrichment of heavy minerals in a layer is controlled by the segregation of a heavy mineral fraction from the light counterpart, which enhances current understanding of heavy mineral placer formation.     

Native gold in complex Ti–Zr placers of the southern West Siberian Plain

Typomorphic features of native gold and its contents in complex Ti–Zr placers in the southern West Siberian Plain are reported. Three of the placers are of littoral-marine genesis, and two formed under conditions of an alluvial piedmont plain. Native gold from the studied Ti–Zr placers occurs mainly as flattened thin (?0.1 mm) particles which underwent mechanical action. It is marked by wide fineness variation and the abundance of a very fine (990–1000‰) variety. Most likely, this is chemically transformed clastogenic metal. The gold content of the productive bed (5–30 mg/m³ native gold and 8–140 ppb bulk gold) is consistent with the dispersion of heavy ore and accessory minerals during mechanical migration in water flows simultaneously with their concentration on geochemical barriers. The native-gold content of complex Ti–Zr placers shows a higher negative correlation with the primary source–placer distance than those of Ti and Zr minerals and a positive correlation with the degree of hydrodynamic reworking (gravity concentration) of transit terrigenous material. On the southern framing of the West Siberian Plain, some regions of northern Kazakhstan are promising for gold of complex Ti–Zr placers as well as fine- and thin-gold placers, gold-bearing weathering crusts, and primary gold deposits.     

Electrokinetic properties and flotation behaviour of apatite and calcite in the presence of sodium oleate and sodium metasilicate

Calcite is generally associated with apatite minerals in phosphate deposits. To explore the possibility of separating these minerals by a soap flotation technique, their electrokinetic properties and flotation behaviour were studied in the presence of sodium oleate.Microelectrophoresis data indicate oleate adsorption on these minerals, and from Hallimond-tube flotation tests it has been noted that in a controlled pH environment and for a certain sodium oleate concentration range, separation of these minerals is possible.The study of apatite/calcite-sodium metasilicate-sodium oleate systems indicates the preferential adsorption of silicate at the calcite surface. This suggests the potential use of sodium metasilicate as the modifying agent for the separation of apatite from calcite by depressing calcite when using sodium oleate as collector.