Geochemical assessment of Paleocene limestones of Sinn El-Kaddab Plateau,South Western Desert of Egypt,for industrial uses

The present work assesses the potential industrial uses of Paleocene limestone deposits, Garra Formation in Sinn El-Kaddab Plateau, South Western Desert of Egypt, based on their mineralogy and geochemical characteristics. Eighty-six limestone samples collected from ten stratigraphic columnar sections were analyzed using X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques. Petrographically, Garra limestone deposits consist dominantly of benthic foraminiferal wackestone and packstone microfacies. The XRD data revealed dominance of low-Mg calcite as essential carbonate mineral in the studied limestone. The bulk rock XRF results revealed CaO (29.28–55.75%) with an average of 52.74%. The CaO exhibits a strong negative correlation with MgO, SiO₂, TiO₂, Al₂O₃, and moderate negative correlation with Fe₂O₃ which indicates that the contribution of these elements is mainly due to detrital input. On the other hand, Al₂O₃ and Na₂O contents exhibit significant negative correlation with loss of ignition (LOI) wt% indicating their incorporation within terrigenous matrix. The average Sr content attains 1297 ppm indicating deposition in temperate marine environment. The average molar CaCO₃% values of bulk samples have been computed for individual columnar sections to determine the purity status of Garra limestone deposits. They range from impure (CaCO₃%?=?79.92%) to high-pure (CaCO₃%?=?97.76%) limestone. Therefore, Garra limestone deposits have extremely valuable uses in a wide spectrum of industrial applications including Portland cement, steel, ceramics, whiting, chemical uses, paper, and feed stuff.     

Re‐creation of the 1744 Heylyn and Frye ceramic patent wares using Cherokee clay: Implications for raw materials,kiln conditions,and the earliest English porcelain production

Porcelain wares have been produced following the directions contained in the Heylyn and Frye patent of 1744, using Cherokee clay and a lime‐alkali glass frit. The wares were fired to the bisque (˜ 950°C), glazed using a clay‐glass mixture, and then fired to a “heat‐work” level of Orton cone 9–90° deflection at 150°C per hour (1279°C). Modal mineralogy comprises Caplagioclase and two glass phases, one relict frit and the other a melt phase. The bulk chemistry of the body comprises 64.3 wt % SiO₂, 21.7 wt % Al₂O₃, and 5.6 wt % CaO. Molecular ratios are SiO₂:Al₂O₃ 5.0 and SiO₂:CaO 10.7. It is concluded that the patent, whose significance has been questioned over many years, was a practical working recipe, that close comparison may be made with porcelains of the “A”‐marked group, and that the patent represents a remarkable landmark in English ceramic history. © 2004 Wiley Periodicals, Inc.     

Mineralogy, geochemistry, and reserve estimation of the Euphrates limestone for Portland cement industry at Al-Najaf area, South Iraq

This study deals with the mineralogical and geochemistry of the Euphrates Formation (Lower Miocene) in Bahr Al-Najaf area in order to assess the lithofacies of the Euphrates Formation for Portland cement manufacturing. Petrographic and mineralogical studies were carried out on 210 core samples, collected from 21 boreholes, and showed that calcite is the dominant mineral with few amounts of quartz, gypsum, feldspar, and a rare amount of dolomite. Clay mineral suites (palygorskite, kaolinite, montmorillonite, and illite) formed about 5% from the total mineral composition. Palygorskite precipitated directly in alkali shallow water rich with Si and Mg ions. Chemical weathering of feldspar under acidic conditions participated in formation of Kaolinite. Geochemistry showed that there is no high variation in chemical constituents with depth, and the average of CaO (51.5), MgO (0.83), SO₃ (0.54), SiO₂ (4.3), Fe₂O₃ (0.45), Al₂O₃ (0.93), L.O.I (40.7), Na₂O₃ (0.08), K₂O (0.14), and Cl^- (0.1) qualified the lithofacies of Euphrates Formation to be raw materials suitable for manufacturing the Portland cement. Triangle Block method is applied to estimate the reserve on square area (2?×?2 km²) which is computed to be 63 million tons of medium-tough limestone as potential probable reserve.     

Geochemical Characteristics of Wuyang Siliceous Rocks in the Southern Margin of North China Craton and its Constraint on the Formation Environment of BIF of Tieshanmiao Formation

Precambrian banded iron formation(BIF) is one of the most important mineral resources in China, mostly abundant in the North China Craton(NCC) with relatively less common in South China. Since the BIF and siliceous rocks both originated from chemical deposition, the syngenetic BIF and Siliceous rocks can help evaluate their environment of formation. We examine here the mineralogy and geochemistry of siliceous rocks associated with the Tieshanmiao Formation BIF, aiming to decipher the conditions of formation of both BIF and Siliceous rocks in the Wuyang area in the NCC. Analysis of the geochemical characteristics of whole rock shows that the Si O2 content of the siliceous rock ranges from 90.11% to 94.85% and is relatively high overall. Trace element contents of Ba and U are also high, the Ba/Sr ratio ranges from 3.89 to 25.28 and the U/Th ratio ranges from 0.09 to 0.20. Finally, the ΣREE value of rare earth elements ranges from 57.03 ppm to 152.59 ppm, and these indexes all indicate that siliceous rock resulted from hydrothermal deposition. Plots of Al2 O3-Si O2, Si O2/(K2 O+Na2 O)-Mn O2/Ti O2 and Mn-10×(Cu+Co+Ni)-Fe in discrimination diagrams also verify this interpretation. However, both the Mg O content, ranging from 0.16 to 0.32, and the Fe/Ti ratio, ranging from 2.50 to 9.72, suggest that terrigenous material was added during the depositional process. Major and trace element parameters of siliceous rock, such as the Al/(A1+Fe+Mn) ratio(from 0.81 to 0.93), Mn O/Ti O2(from 0.00 to 0.17), Al/(Al+Fe)(from 0.82 to 0.93), Sc/Th ratio(from 0.21 to 0.50), U/Th(from 0.09 to 0.20),(La/Yb)N(from 0.83 to 3.04), and the(La/Ce)N(from 0.01 to 0.02) all imply that the siliceous rock formed in a continental margin. In addition, the Sr/Ba ratio from 0.08 to 0.26, the δCe value from 0.31 to 0.90, and the δEu value from 0.14 to 0.58, all indicate that the siliceous rock was formed at a relatively deeper water depth and under weak hydrodynamic conditions. Siliceous rock and BIF formed in the same geological setting, with the Si O2/(K2 O+Na2 O) ratio of siliceous rock ranging from 28.61 to 47.43, the Si O2/Al2 O3 ratio from 16.53 to 32.37, and the Si O2/Mg O ratio from 287.28 to 592.81, which are all in agreement with chemical deposition associated with volcanic eruptions. The Al2 O3/Ti O2 ratio from 37.82 to 50.30 indicates that the magma source of siliceous rock was of slightly intermediate composition. During the Late Archean in the Wuyang area, the high concentration and high purity Si O2 quickly precipitated from hydrothermal fluids to finally result in the accumulation of siliceous rock in a marginal sea, while the input corresponding to iron formation components was deposited to form iron formation layers, and limestone was only the product formed during the deposition intervals of siliceous rock and iron formations. In this study, the synsedimentary siliceous rocks of BIF act as a new way to provide direct evidence to understand the formation environment of BIF due to its high geochemical stability.     

Assimilation of the mafic‐ultramafic magma: a case study of diabase dyke at the Beidaihe,North China Craton

Assimilation serves as a significant part in magma's evolution. Because of rapid cooling of ultramafic‐mafic magma, assimilation between mantle‐derived magma and crustal rocks (wall‐rocks) is often neglected. The Beidaihe diabase dikes in North China Craton suggest that assimilation of the rapidly cooled mantle‐derived magma can not be ignored. The diabase dikes are very thin (0.5 to 2 m in width) and discordantly intrude into Ordovician limestone. Center of dyke is porphyritic texture while chilled margin of it is aphanitic texture, suggesting a rapid crystallization process. Moreover, limestone close to the dyke was transformed into marble because of contact‐thermal metamorphism. From the center to margin of the dykes, contents of SiO₂ (48.9→ 41.6 wt.%) and MgO (8.3 → 4.0 wt.%) are obviously decreased, but contents of CaO (6.4→8.3 wt.%) and CO₂ (0.8 → 5.2 wt.%) are distinctly increased. Meanwhile, calcites in the wall rocks adjacent to and far from the dykes are also greatly different. The calcites close to the dykes have high MgO and FeO contents but low CaO and CO₂ contents. All these suggest an assimilation process of the mantle‐derived magma with wall‐rock limestone. Calculating CO₂ contents in the dyke and wall rock suggest that the extent of assimilation is thought to reach up to 8 ‐ 12 %. Therefore, when the wall rocks of the mantle‐derived magma are carbonate rocks, its components are obviously influenced by assimilation, although it often rapidly chilled. Simultaneously, this study provides possible explanation for some mantle‐derived rocks in carbonate areas with high LOI.     

Mineralogical and geochemical investigation of clay-rich mine tailings from a closed phosphate mine, Bartow Florida, USA

Clay-rich mine tailings from phosphate mine operations in Florida are a major environmental and economic problem. Options for reclamation and restoration for these tailings are very limited and are fundamentally restricted by poor physical properties such as low mechanical strength, low hydraulic conductivity, and heavy metal content. The major control on these bulk physical properties is the mineralogy of the materials. Eight continuous push borings were obtained to investigate stratigraphy, mineralogy, aspects of geochemistry, and bulk properties of a deposit of clay-rich mine tailings from a phosphate mine near Bartow, Florida that ceased operations in the early 1970s. Stratigraphy is dominated by laminated clay-rich sediment with minor units of silt and sand. An intact kaolinite liner occurs near the impoundment walls and the impoundment floor has approximately 4 m of relief. Moisture content varies from 4.35 to 57.40 wt% and organic content varies from 0.41 to 9.53 wt%. Bulk XRF investigation indicates that the P₂O₅ concentrations vary from approximately 4 to 21 wt%. A very strong correlation (r ² = 0.92) between CaO and P₂O₅ indicates that apatite is a major control on the phosphate. The strong correlation (r ² = 0.77) of Al₂O₃ and TiO₂ suggests that the source materials for this deposit are comparatively uniform. A number of heavy metal elements and trace elements occur. Cr, V, Ni, Cu are interpreted to be in phosphate minerals, largely apatite. Sr and Pb are interpreted to be in both phyllosilicates and phosphate minerals. Two populations of apatite were observed in the clay-sized fraction, one that was Fe and Si- bearing and another that was only Si-bearing. Fe-bearing apatite had Fe₂O₃ contents that varied from 0.38 to 5.32 wt% and SiO₂ contents that varied from 0.90 to 3.32 wt%. The other apatite population had a wider range of SiO₂ contents that varied from 0.77 to 8.80 wt%. TEM imaging shows that apatite grains are dominantly single crystals with lesser amounts of aggregates. Wavellite commonly occurs as individual or clusters of lath-like crystals and the chemical composition differs from the pure aluminium phosphate end member with average concentrations of components being that of CaO (1.57 wt%), Fe₂O₃ (1.98 wt%), SiO₂ (5.94 wt%). In the clay-sized phosphate minerals investigated no fluorine was found above detection limit (approximately 0.15 wt%), nor was any uranium, radium, heavy metal, or REE element detected. The phyllosilicate mineralogy of the deposit is dominated by smectite (montmorillonite with lesser amounts of nontronite), palygorskite, illite and kaolinite. No systematic variation in the relative proportions of phyllosilicates was observed in the clay deposit. Energy dispersive spectroscopy EDS analysis indicates that chemical compositions of phyllosilicates are somewhat typical but overall are enriched with respect to Fe compared to theoretical end members. The relative enrichment of Fe is interpreted to be a primary sedimentary feature. Ca content in smectite minerals is high and may inhibit stabilization using lime or similar methods. The high percentages of montmorillonite and palygorskite explain the high bulk water contents observed. This investigation provides fundamentally new details regarding clay tailing deposits from closed phosphate mines in central Florida which can be used in restoration and reclamation efforts.     

Calcic hydrosilicate metasomatic rocks at the Gumeshevsk skarn-porphyry copper deposit in the central Urals,Russia

The body of hydroxylellestadite metasomatic rock penetrated by a borehole drilled at the Gumeshevsk deposit at depths of 530–534 m includes a thin interval of younger lower temperature tobermorite-plombierite metasomatic rock with subordinate amounts of Ca-Si gel, tacherenite, cubic lime, and thaumasite. Hydroxylellestadite has never before been found in calc skarns. The hydroxylellestadite metasomatic rock is cut by gypsum and fukalite veinlets, and the tobermorite-plombierite metasomatic rock is intersected by thaumasite veinlets. The pristine rock of the metasomatics was marble, and the metasomatic rock replaced andradite-bearing wollastonite skarn (with wollastonite replaced by foshagite). The ore minerals (chalcopyrite, valleriite, sphalerite, and others) were formed after the hydroxylellestadite metasomatite but most probably before the tobermorite-plombierite metasomatic rock and the veinlets of calcic minerals. The metasomatic rock was produced at significant variations in the oxygen, sulfur, and carbon dioxide fugacities. The composition of the hydroxylellestadite is, according to its microprobe analysis, as follows (wt %): SiO₂ 17.10, TiO₂ 0.01, Al₂O₃ 0.02, FeO 0.20, MnO 0.00, MgO 0.04, CaO 55.40, Na₂O 0.14, K₂O 0.09, P₂O₅ 0.12, CO₂ 1.90 (chemical analysis), SO₃ 21.60, F 0.16, Cl 0.14, total 96.92. The plombierite (SiO₂ 43.8–44.1 wt %, CaO 30.5–31.1 wt %) in the metasomatic rock notably differs from rare plombierite (SiO₂ 48.18 wt %, CaO 39.19 wt %) contained in the veinlets of thaumasite (SiO₂ 12.70 wt %, CaO 30.69 wt %, SO₃ 17.78 wt %).     

Hydrothermal alteration of oceanic basalts by seawater

Hydrothermally altered pillow basalts dredged from the Mid-Atlantic Ridge, and belonging to the greenschist facies, have been studied in order to determine the mineralogical and corresponding chemical changes, that result from basalt-seawater interaction at elevated temperatures.The mineralogical transformations are predominantly to albite-actinolite-chlorite-epidote assemblages. Quartz and pyrite are common accessory minerals. On the basis of their mineralogy, the samples may be divided into chlorite-rich and epidote-rich assemblages. The chlorite-rich assemblages, which are the predominant variety, show the greatest chemical changes, while the epidote-rich samples show very little change in composition compared with their basaltic precursors.Mass balances across individual pillows in which the central portions are relatively unaltered allow the directions and ranges of elemental fluxes to be calculated. In general, SiO₂ and CaO are leached from the basalt, while MgO and H₂O are taken up. No consistent trends are observed for Na₂O and K₂O although they do show some variations in the core-and-rim analyses.Consideration of the elemental fluxes in terms of steady-state geochemical mass balances for oceanic inputs and outputs indicates that hydrothermal alteration provides a sink for Mg, which may be extremely important in solving the problem of apparent excess Mg input to the oceans. The amount of Ca that is leached from the rock may be of significance in the geochemical budget of that element. The amount of SiO₂ in the circulating fluid is controlled by the solubility of quartz or amorphous silica, depending on temperature, and considerable redistribution of silica takes place within the basaltic pile. The changes in redox conditions during hydrothermal alteration do not affect the present day oxidation state of the atmosphere and hydrosphere.     

Geochemistry of the Eocene limestones of the Jaisalmer basin,Rajasthan, India: Implications on depositional conditions and sources of rare earth elements

Major, trace and rare earth elements (REE) concentration of the Eocene limestones, Jaisalmer Basin, Rajasthan, India are analysed to reconstruct the depositional conditions and to identify sources of REEs. Among the major oxides, CaO is the dominant oxide followed by SiO₂ in the studied limestones. Trace element Ba dominates over the other trace elements and it shows negative correlation with CaO. The Sr, occurring in small concentration, shows positive correlation with CaO. Other trace elements such as V, Zr, Sc, Y, Rb, Ni, Pb Co, Cu, U occur in small concentrations. The studied limestones show a positive correlation of ΣREE with Fe₂O₃, Ni, Th, Sc, and Y. These limestones possess sea-water like shale-normalized REE + Y pattern with light REE depletion, slight Gd enrichment, slightly positive La anomaly, positive Y anomaly, positive Eu anomaly, negative Ce anomaly and superchondritic Y/Ho ratio from 23.12 to 28.57. The dominance of CaO and low percentage of MgO suggest that mineral phase is calcite and there is absence of dolomitization. The occurrence of SiO₂ and Al₂O₃ in appreciable percentages may be because of the siliciclastic input during the limestone precipiatetion. The low concentration of Uranium (0.4-3.7) and authigenic Uranium (Average Total U-Th/3 value = 0.74) indicate that the studied limestones were precipitated in oxic condition from seawater. The depletion of LREE suggests that the limestones were precipitated from the seawater. The positive correlation of ΣREE with Al₂O₃ Fe₂O₃, Ni, Th, Sc, and Y and negative correlation with CaO suggest an input of siliciclastic sediments from the land during limestone precipitation. The negative Ce anomaly, slightly positive La anomaly, slight Gd enrichment, positive Y anomaly, and positive Eu anomaly also suggest that the limestone was precipitated from the seawater with some siliciclastic input from continent. The low values of the Y/Ho ratio (23.12 to 28.57) in the studied limestones suggest some modification of the seawater by the input of freshwater in a coastal environment. The REEs of the studied limestones are correlable with the shallow sea water REEs with exception of a few elements. We envisage a coastal/shallow marine depositional environment where mixing of the continental material in sea water appears feasible.     

我国硅灰石矿床成因类型及地质特征

前言在我国,硅灰石是一种新兴的工业矿物原料。自1975年于湖北省大冶县小箕铺发现有一定规模的硅灰石矿床以来,我国硅灰石地质及其工业应用的研究发展很快。短时间内找到并探明了一批质量好、又有一定规模的硅灰石矿床;以硅灰石为主要原料的低温快烧釉面砖的研     

Are spatial distributions of major elements in soil influenced by human landscapes?

The present study attempted to evaluate the influence of human activity on major elements (Na₂O, MgO, Al₂O₃, SiO₂, K₂O, CaO, Fe₂O₃), and to find a method to explore correlations between major elements and human disturbances, according to geospatial theories and methods. The study results indicate that landscapes influence major elements in diverse ways: Al₂O₃ is closely related to road and mine landscapes; strong relationships exist between MgO, Fe₂O₃, CaO, and SiO₂ and roads; Na₂O, SiO₂, and Fe₂O₃ are unrelated to city landscapes; and Na₂O is unrelated to road and mine landscapes.     

Composition and genesis of inner-contact syenites of the Khasurta quartz syenite-monzonite massif,western Transbaikalia

The paper reports data on the geological structure, mineralogy, and geochemistry of inner-contact syenites of the Late Paleozoic Khasurta quartz syenite-monzonite massif in western Transbaikalia. The rocks of the massif intrude Cambrian terrigenous-carbonate deposits transformed (depending on their composition) into apodolomitic magnesian spinel-fassaite skarns or plagioclase-quartz-biotite-cordierite hornfels that replaced amphibole-biotite schists. The skarn zone does not exceed a few dozen centimeters in thicknes. The inner-contact zone of the intrusion a few dozen meters thick consists of leucocratic medium-grained pyroxene syenites, which consist of coarsely perthitic K-Na feldspar (90–95 vol %) with plagioclase (An _40–46) cores, zonal clinopyroxene (up to 5–7 vol %), and sphene (up to 3–4 vol %). The inner-contact syenites differ from all other rocks of this massif in having the highest alkalinity and elevated concentrations of SiO₂ and the lowest contents of CaO, MgO, and FeO. The mineralogical composition of the inner-contact syenites makes them similar to skarn-related metasomatic rocks (Korzhinskii, 1948), but the pyroxenes of these rocks contain melt inclusions homogenizing at 1100°C, a fact testifying to the magmatic genesis of the rocks. The results of our research indicate that the inner-contact syenites were formed with the assimilation of the host dolomites by the syenite melt. The enrichment of the inner-contact syenite melt in CaO and MgO and a significant increase in its liquidus temperature due to CO₂ dissolution (Jahannes and Holtz, 1996) facilitated the crystallization of calcic plagioclase, pyroxene, and magnetite. The fractionation of these minerals resulted in the enrichment of the residual melt in SiO₂ and alkalis, mostly K₂O, and this subalkaline residual melt produced that K-Na feldspar, which is the predominant mineral of these rocks, and sphene. Excess CO₂ drastically suppressed the H₂O activity in the melt and thus hampered the crystallization of amphibole and biotite in the inner-contact zone of the intrusion. Mass-balance calculations indicate that dolomite assimilation was not very extensive and did not exceed 1: 10.     

Geochemical dissociation of major and trace elements in bed and suspended sediment phases of the phosphate mines effluent water, Jordan

The bed and suspended (slime) sediment phases associated with effluent water that are produced from phosphate-ore-upgrading process at Al-Abyad mine in the southern part of Jordan were analyzed chemically and mineralogically. The results show that the effluent water is highly oxic and mildly alkaline in nature. The geochemical behavior of each phase was controlled by the effluent water physicochemical parameters, sediment particle size, mineralogical constituents of the studied phases, and the prevailing climatic nature of the area. Bed sediments have higher concentrations of many elements than slime. Accordingly, the bed sediments can be considered as a sink rather than a pool for many elements. The geochemical dissociation of major oxides and trace elements between bed and slime sediments was evident using t test, particularly between P₂O₅, SiO₂, CaO, K₂O, Mn, Sr, Y, and Co, and to lesser extent, V, U, Zn, and Cr. This might be attributed to effluent water characteristics, mineralogy, and the presence of fine-grained materials. The spatial distribution of major oxide and trace element concentrations along the stream drainage exhibited a slight increase with distance either in bed or slime sediment phases. However, they increased suddenly at the last three sampling sites, which might be due to the abundance of fine-grained materials that are mainly composed of clay minerals (montmorillonite) that would enhance the adsorption process. Moreover, the XRD results confirmed the existence of elemental geochemical dissociation as a function of mineral control.     

Geochemical and palynological analyses of the Serikagni Formation, Sinjar, Iraq

Serikagni Formation (lower–middle Miocene) was studied at four outcrop sections within Sinjar Anticline, Para (the western plunge), Jaddala, Sinjar, (Southern limb), and Noaniaa (Northern limb) of Sinjar Mountain, which is part of foothill zone in northwest Iraq. This formation is composed of Globigerina limestone, marly limestone intercalated with marl, deposited in quiet, deep marine environment. Palynological analyses and the percentages of palynological matter were determined. Palynofacies analysis was recorded for paleoenvironmental interpretation. Mineralogical investigations and petrographical analyses were done. Geochemical analyses for the determination of the major constituents (CaO, MgO, and I.R.),the secondary constituents (SiO₂, Al₂O₃, Fe₂O₃, Na₂O, K₂O, and trace elements (Sr, Mn, Cu, Zn, Co, Cr, Pb) in the rock samples were accomplished. The calcite is the predominant mineral which is mostly of micrite types as well as spary calcite. The insoluble residue (I.R.) has negative correlation with the carbonate percentages in the rock formation as observed by the XRD analyses. Clay minerals show low occurrence represented by palygorskite, montmorillonite, and sepiolite. Geochemical differences can be noticed between the limy and marly facies constituting the same formation. Differences are also observed between the geochemistry and mineralogy of the four studied localities such as the relatively more pure limestone in Jaddala and Para sections than Sinjar and Noaniaa sections which indicate the higher percentages of marly limestone. This is believed to be due to the geographic location of these sections within the main depositional environment, as well as the consequences of sea level fluctuation. Two palynofacies (PF-1) and (PF-2) were identified. Palynomorphs are more numerous with high percentages (>80%) of amorphous organic matter (AOM) is present in the PF-1. The lithological association of this palynofacies is limestone and marly limestone. This palynofacies 1, indicate the deep marine depositional environment. The second palynofacies (PF-2) reflect low quantities (less than 40%) of AOM, with increase of phytoclasts (translucent-type) to more than 30% and the miospores (small spores and pollen grains) to more than 20%. The lithological association of this palynofacies is marl and marly limestone. This palynofacies 2, indicate the nearshore and shallow marine depositional environment.     

Geochemistry of Proterozoic Radioactive Arkoses in Khammam District,Andhra Pradesh,India: Evidence for K-rich Evolved Granitoid Upper Crust in the Late Archaean

Geochemical studies on radioactive arkoses (43–153 ppm U and 387–862 ppm Th) of the Proterozoic Pakhal Supergroup from Bangaruchilka, Khammam district, Andhra Pradesh, India, indicate that their gross major and trace element chemistry reflect their mineral composition. Chemically, arkoses are rich in silica (83% to 88% SiO₂) and potassium (3% to 5% K₂O), with consistently high Al₂O₃/Na₂O (36 to 50) and K₂O/Na₂O (18 to 25) ratios, which indicate that they are chemically mature sediments. The arkoses also show higher concentrations of Ti, V, Cr, Ni, Cu, Y, Zr, Nb, La and Pb.The values (60% to 68%) of chemical alteration index (CIA) of studied arkoses are moderate, and indicate that the source rocks have undergone lesser degree of chemical weathering. Tectonic setting discriminate plots of Fe₂O₃ (total)/MgO vs. TiO₂ and Al₂O₃/SiO₂, and K₂O/Na₂O vs. SiO₂ and SiO₂/Al₂O₃ indicate that the Bangaruchilka arkoses represent the sediments that were deposited in passive continental margin (PM), which is further supported by association of platformal type of sediments (quartzites and phyllites) with them. Unlike middle Archaean sedimentary rocks, the studied arkoses are depleted in Na₂O, MgO and CaO, and distinctly enriched in SiO₂ and K₂O. These geochemical features match with post-Archaean clastic sediments, which argues for the involvement of late Archaean granitic crust in supply of detritus of studied arkoses. Enrichment of potassium alongwith abundant microcline and elevated concentrations of Y, Zr, Nb, U, Th, La, etc. in arkoses indicate K-rich evolved granitoid upper crust in the provenance during the late Archaean-early Proterozoic period.Dominance of mechanical weathering over chemical weathering favoured arkose formation, and also transfer of radio-elements with clastic sediments into the Pakhal basin. After sedimentation, uranium seems to have been remobilised from the rocks of Archaean-Pakhal system, consequent to post-sedimentation structural disruptions, and concentrated along suitable structural loci. Therefore, it is likely to encounter significant concentration of uranium in close proximity of unconformable Archaean and Pakhal contacts and tectonic zones, thereby making Pakhal basin and its environs a suitable terrain to search for concealed uranium mineralisation.     

Production of Bauxite Certified Reference Material (BARC-B1201) for Nine Property Values (Al2O3, Fe2O3, SiO2, TiO2, V2O5, MnO,Cr2O3, MgO and LOI) Traceable to SI Units

The National Centre for Compositional Characterisation of Materials (NCCCM) / Bhabha Atomic Research Centre (BARC) and National Aluminium Company Limited (NALCO), India have produced an Indian origin bauxite certified reference material (CRM), referred to as BARC-B1201, certified for major (Al₂O₃, Fe₂O₃, SiO₂, TiO₂, loss on ignition - LOI) and trace contents (V₂O₅, MnO, Cr₂O₃, MgO). Characterisation was undertaken by strict adherence to ISO Guides. A method previously developed and validated in our laboratory, using single step bauxite dissolution and subsequent quantitation (of Al₂O₃, Fe₂O₃, SiO₂, TiO₂, V₂O_5, MnO, Cr₂O₃ and MgO) by ICP-AES (SSBD ICP-AES) was used for homogeneity studies and an inter-laboratory comparison exercise (ILCE) of the candidate CRM. LOI was determined by thermo-gravimetric analysis. Property values were assigned after an ILCE with participation from seventeen reputed government and private sector laboratories in India. The CRM was certified for nine property values: Al₂O₃, Fe₂O₃, SiO₂, TiO₂, V₂O_5, MnO, Cr₂O₃, MgO and LOI, which are traceable to SI units.     

Chemical study of limestone and clay for cement manufacturing in Darukhula,Nizampur District,Nowshera, North West Frontier Province （N.W.F.P.）, Pakistan

Limestone and clay samples were collected from Darukhula and adjoining areas of the Nizampur District Nowshera, N.W.EE, Pakistan, and analyzed for different parameters in order to search for new reserves of suitable material for the manufacture of different types of cements in N.W.F.P. It was found that the area under study contains three types of limestones, including high grade limestone, Darukhula limestone and siliceous limestone, which contain 53%, 49.03% and 45.19% CaO, respectively, and three types of clay, including maroon color, yellow to yel- lowish-green color and green color clay containing 57.76%, 65.47% and 61.24% SiO2, respectively. Chemical analysis of the limestone and clay samples collected from the deposits in the area under study showed that all the elements found in these samples are within the range of permissible limits for the production of high-strength Portland cement, sulphate resisting cement and white cement. This paper covers the detailed version of the potential raw material deposits at Darukhula and adjoining areas of the Nizampur District.     

昆阳磷矿磷块岩的矿物组成

昆阳磷矿是我国下寒武统最大的磷块岩矿床之一,矿层赋存于下寒武统渔户村组的中谊村段地层中(罗惠麟等,1982),矿层有上、下两层,分别称之为“上磷层”和“下磷层”,中间为一“白泥层”(含磷粘土页岩)分隔(Yeh Lien-tsun et al.,)。含磷岩系的岩性序列特征见图5。罗惠麟等认为,本段地层均为台凹相沉积,其中“下磷层”的形成环境为潮下低能及间歇性高能带,“白泥层”为潮下低能带,“上磷层”为潮下高能带,再往上则向潮间坪过渡。本文研究磷块岩的矿物组成,主要是矿石矿物磷灰石和粘土矿物的特点,并讨论磷灰石成份同矿石类型和形成环境等问题。     

Effectiveness of rice husk ash in stabilizing Kenyan red coffee soil for road subgrades construction

The high cost of traditional stabilizing agents such as lime and cement has led to the research on industrial and agricultural wastes as suitable alternatives. Rice growing areas of Kenya accumulate large quantities of rice husk which pose serious disposal problems. When burnt as a means of disposal, the rice husk ash formed is difficult to coagulate and thus contribute to air and water pollution, require a large space for disposal, and cause respiratory health problems when inhaled. Red coffee soil poses serious engineering problems such as swelling due to wetting, shrinkage due to drying, low bearing capacity, and differential settlement leading to cracks and needs improvement for strength and stability in service. Red coffee soil and rice husks samples were obtained from Gatundu and Mwea, respectively. The rice husk was burnt at temperatures between 500 and 700 °C to ensure maximal formation of siliceous component. Chemical analysis on the rice husk ash gave the sum of SiO₂, Fe₂O₃, and Al₂O₃ as 85.5 % indicating that it has pozzolanic activity. Rice husk ash was applied at 4, 6, 8, and 10 % by weight of dry soil. Plasticity index, liquid limit, and linear shrinkage decreased from 26.1, 67.1, and 13.0 % for lean sample to 18.5, 63.6, and 9.2 %, for 10 % rice husk ash stabilized samples, whereas plastic limit increased from 41.0 to 45.15 %. The soaked California bearing ratio value for rice husk ash stabilized samples increased from 5 to 22 % corresponding to soil subgrade class S4. However, lime-stabilized samples gave higher values.     

Chemistry and origin of chloritoid rocks from eastern Taiwan

Chloritoid-rich rocks occur as thin pods or lenses in the well-foliated marble and greenschist of the pre-Tertiary metamorphic complex of eastern central Taiwan. They contain unusually abundant chloritoid: 60–90% in the massive rocks and 30–50% in the schistose rocks. Compared to the adjacent basaltic greenschist, the chloritoid rocks contain extremely low SiO₂, CaO and Na₂O and very high Al₂O₃, total Fe as Fe₂O₃, and TiO₂. Both monoclinic and triclinic chloritoids were identified. These rocks may have been derived originally from fossil lateritic soils formed from a basaltic layer in a limestone terrain. These soils and the bedded rocks were then metamorphosed in the chlorite-biotite zone of the greenschist facies.