Early diagenetic high-magnesium calcite and dolomite indicate that coal balls formed in marine or brackish water: Stratigraphic and paleoclimatic implications

Science.gov (United States)

Raymond, Anne

2016-04-01

Coal balls are carbonate and pyrite permineralizations of peat that contain three-dimensional plant fossils preserved at the cellular level. Coal balls, which occur in Pennsylvanian and earliest Permian equatorial coals, provide a detailed record of terrestrial ecology and tropical climate during the Late Paleozoic Ice Age; yet their depositional environment remains controversial. The exquisite preservation of some coal-ball fossils, e.g. pollen with pollen tubes and leaves with mesophyll, indicates rapid formation. The presence of abundant, cement-filled, void spaces within and between the plant debris in most coal balls indicates that they formed in uncompacted peat, near the surface of the mire. Botanical, taphonomic and isotopic evidence point to a freshwater origin for coal balls. The nearest living relatives of coal ball plants (modern lycopsids, sphenopsids, marratialean ferns and conifers) grow in fresh water. Coal-ball peat contains a high percentage of aerial debris, similar to modern freshwater peat. The stable oxygen isotopes of coal-ball carbonate (δ18O = 16 to 3 per mil) suggest a freshwater origin. However, the widespread occurrence of marine invertebrates and early diagenetic framboidal pyrite in coal balls suggests that many formed in close proximity to marine water. Indeed, carbonate petrology points to a marine or brackish water origin for the first-formed carbonate cements in coal balls. Petrographic and geochemical (microprobe) analysis of coal-ball carbonates in Pennsylvanian coals from the midcontinent of North America (Western Interior Basin, West Pangaea) and the Ruhr and Donets Basins (East Pangaea) indicate that the first formed carbonate is either radaxial, nonstochiometric dolomite or high magnesium calcite (9 - 17 mol % MgCO3, indicating precipitation in marine or brackish water. Although both primary dolomite and high magnesium calcite can form in lacustrine settings, the lakes in which these minerals form occur in carbonate terranes

Thermal decomposition of dolomite under CO2: insights from TGA and in situ XRD analysis.

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Valverde, Jose Manuel; Perejon, Antonio; Medina, Santiago; Perez-Maqueda, Luis A

2015-11-28

Thermal decomposition of dolomite in the presence of CO2 in a calcination environment is investigated by means of in situ X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The in situ XRD results suggest that dolomite decomposes directly at a temperature around 700 °C into MgO and CaO. Immediate carbonation of nascent CaO crystals leads to the formation of calcite as an intermediate product of decomposition. Subsequently, decarbonation of this poorly crystalline calcite occurs when the reaction is thermodynamically favorable and sufficiently fast at a temperature depending on the CO2 partial pressure in the calcination atmosphere. Decarbonation of this dolomitic calcite occurs at a lower temperature than limestone decarbonation due to the relatively low crystallinity of the former. Full decomposition of dolomite leads also to a relatively low crystalline CaO, which exhibits a high reactivity as compared to limestone derived CaO. Under CO2 capture conditions in the Calcium-Looping (CaL) process, MgO grains remain inert yet favor the carbonation reactivity of dolomitic CaO especially in the solid-state diffusion controlled phase. The fundamental mechanism that drives the crystallographic transformation of dolomite in the presence of CO2 is thus responsible for its fast calcination kinetics and the high carbonation reactivity of dolomitic CaO, which makes natural dolomite a potentially advantageous alternative to limestone for CO2 capture in the CaL technology as well as SO2in situ removal in oxy-combustion fluidized bed reactors.

First discovery of dolomite and magnesite in living coralline algae and its geobiological implications

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M. C. Nash

2011-11-01

Full Text Available Dolomite is a magnesium-rich carbonate mineral abundant in fossil carbonate reef platforms but surprisingly rare in modern sedimentary environments, a conundrum known as the "Dolomite Problem". Marine sedimentary dolomite has been interpreted to form by an unconfirmed, post-depositional diagenetic process, despite minimal experimental success at replicating this. Here we show that dolomite, accompanied by magnesite, forms within living crustose coralline alga, Hydrolithon onkodes, a prolific global tropical reef species. Chemical micro-analysis of the coralline skeleton reveals that not only are the cell walls calcitised, but that cell spaces are typically filled with magnesite, rimmed by dolomite, or both. Mineralogy was confirmed by X-ray Diffraction. Thus there are at least three mineral phases present (magnesium calcite, dolomite and magnesite rather than one or two (magnesium calcite and brucite as previously thought. Our results are consistent with dolomite occurrences in coralline algae rich environments in fossil reefs of the last 60 million years. We reveal that the standard method of removing organic material prior to Xray Diffraction analysis can result in a decrease in the most obvious dolomite and magnesite diffraction patterns and this may explain why the abundant protodolomite and magnesite discovered in this study has not previously been recognized. This discovery of dolomite in living coralline algae extends the range of palaeo-environments for which biologically initiated dolomite can be considered a possible source of primary dolomite.

Geochemistry and origin of regional dolomites

International Nuclear Information System (INIS)

Hanson, G.N.; Meyers, W.J.

1989-12-01

The major goal of the carbonate research program at Stony Brook is to better understand the conditions and processes leading to regional diagenesis of carbonate rocks. Our research focuses on studies of ancient, massive dolostones, but we are also studying limestone diagenesis for its own importance, and as it relates to dolomitization. Our approach has been to carry out a very detailed petrographic and geochemical case study to the Mississippian Burlington-Keokuk Fms. of Iowa, Illinois and Missouri, and to develop this as a testing ground for new geochemical and modelling techniques, and for testing various models for regional dolomitization in epicontinental carbonates. The ideas and techniques developed in our Burlington-Keokuk studies are being expanded and applied to carbonate sequences of other ages (Devonian to Neogene), and other tectono-sedimentary settings. The emphasis of this report will be on new developments and results on the Burlington-Keokuk studies and on our diagenetic studies of other strata. Recent research on Burlington-Keokuk rocks include development and application of boron isotopes and the U--Th--Pb system to dolomite studies, investigations of porosity and permeability in the dolostones. Projects on other strata include dolomitization and limestones diagenesis of Devonian carbonates of Alberta and Western Australia, Miocene reefal carbonates of Spain, Neogene carbonates of Curacao and Bonaire, Waulsortian limestones of Ireland, modelling of trace elements and stable isotopes, and experimental growth of calcites to investigate crystallographic controls of trace element incorporation. 118 refs., 46 figs

Differences in the rheological properties of calcitic and dolomitic lime slurries: influence of particle characteristics and practical implications in lime-based mortar manufacturing

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Arizzi, A.

2012-06-01

Full Text Available The study of the rheological properties of lime suspensions is a useful means to evaluate the workability of lime mortars. In this work, we studied the flow behaviour of two industrial hydrated limes, one of calcitic and the other of dolomitic composition, by means of two types of rheometer with different geometry and setup mode. The obtained results were interpreted taking into account the differences in microstructure and surface properties of the suspended particles. Calcitic lime dry particles are formed by angular and polydisperse clusters and, once dispersed in water, they behave like thixotropic materials. On the other hand, the dolomitic lime is formed by nanoparticles and small round cluster and it shows a pronounced plastic behaviour in suspension. This fundamental difference between the two materials explains the traditional preference for dolomitic lime mortars for plastering and rendering applications.

El estudio de las propiedades reológicas de suspensiones de cal es una herramienta muy útil para evaluar la trabajabilidad de morteros de cal. En este trabajo se ha estudiado el comportamiento en suspensión de dos cales hidratadas, de composición calcítica y dolomítica, mediante dos tipos de reómetros con geometría y modalidades distintas de medida. Los resultados obtenidos se han interpretado teniendo en cuenta las diferencias en la microestructura y las propiedades de superficie de las partículas en suspensión. Las partículas de cal calcítica están formadas por aglomerados angulares y polidispersos y, una vez dispersadas en agua, presentan un comportamiento tixotrópico. Por su parte, la cal dolomítica está formada por nanopartículas y pequeños agregados redondeados y muestra en suspensión un pronunciado comportamiento plástico. Esta importante diferencia entre las dos cales explica la preferencia tradicional de morteros de cal dolomítica para aplicaciones en revocos.

Dolomitization and sedimentary cyclicity of the Ordovician, Silurian, and Devonian rocks in South Estonia

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Kallaste, Toivo

2006-03-01

Full Text Available The distribution and composition of dolomitized rocks and stoichiometry of dolomite in southern Estonia in the Ordovician, Silurian, and Devonian were studied on the background of the facies, sedimentary cyclicity (nine shallowing-up cycles, and evolution of the palaeobasins. The composition of rocks and lattice parameters of dolomite were investigated using the X-ray diffraction, X-ray fluorescence, titration and gravimetric analyses, and porosity measurements. The formation of dolostones is directly determined by the cyclic evolution of palaeobasins. Dolomitized rocks belong to the shallow-water inner shelf or tidal/lagoonal facies belt of regressive phases of sedimentary cycles. Sediments of the deep shelf/transitional environment and transgressive phases are not dolomitized. The most stoichiometric is secondary replacive dolomite of Silurian and upper Ordovician dolostones, formed during the early diagenesis of normal-marine (saline shallow-shelf calcitic sediments. The content of insoluble residue does not affect the stoichiometry. The changes in lattice parameters are induced by the Ca/Mg ratio in the dolomite lattice. The dolomite of the dolostones contacting limestone or containing calcite has an expanded lattice. The primary (syngenetic dolostone of the lagoonal or tidal flat belt has also an expanded lattice. No dolomitizing effect of the waters of the Devonian palaeobasin on the underlying rocks was revealed. The whole data set of the studied dolostones is consistent with the marine water environment in the palaeobasin at the corresponding time and shows no sign of the inflow of external fluids. It suggests that the microbial model of dolomite formation may characterize the Ordovician, Silurian, and Devonian in southern Estonia. The occurrence of dolostones between undolomitized rocks limits the time of dolomitization to the early diagenetic stage.

Insights into the dolomitization process and porosity modification in sucrosic dolostones, Avon Park Formation (Middle Eocene), East-Central Florida, U.S.A.

KAUST Repository

Maliva,, Robert G.

2011-03-01

The Avon Park Formation (middle Eocene) in central Florida, U.S.A., contains shallow-water carbonates that have been replaced by dolomite to varying degrees, ranging from partially replaced limestones, to highly porous sucrosic dolostones, to, less commonly, low-porosity dense dolostones. The relationships between dolomitization and porosity and permeability were studied focusing on three 305-m-long cores taken in the City of Daytona Beach. Stable-isotope data from pure dolostones (mean δ 18O = +3.91% V-PDB) indicate dolomite precipitation in Eocene penesaline pore waters, which would be expected to have been at or above saturation with respect to calcite. Nuclear magnetic log-derived porosity and permeability data indicate that dolomitization did not materially change total porosity values at the bed and formation scale, but did result in a general increase in pore size and an associated substantial increase in permeability compared to limestone precursors. Dolomitization differentially affects the porosity and permeability of carbonate strata on the scale of individual crystals, beds, and formations. At the crystal scale, dolomitization occurs in a volume-for-volume manner in which the space occupied by the former porous calcium carbonate is replaced by a solid dolomite crystal with an associated reduction in porosity. Dolomite crystal precipitation was principally responsible for calcite dissolution both at the actual site of dolomite crystal growth and in the adjoining rock mass. Carbonate is passively scavenged from the formation, which results in no significant porosity change at the formation scale. Moldic pores after allochems formed mainly in beds that experienced high degrees of dolomitization, which demonstrates the intimate association of the dolomitization process with carbonate dissolution. The model of force of crystallization-controlled replacement provides a plausible explanation for key observations concerning the dolomitization process in the

Insights into the dolomitization process and porosity modification in sucrosic dolostones, Avon Park Formation (Middle Eocene), East-Central Florida, U.S.A.

KAUST Repository

Maliva,, Robert G.; Budd, David A.; Clayton, Edward A.; Missimer, Thomas M.; Dickson, John Anthony D

2011-01-01

The Avon Park Formation (middle Eocene) in central Florida, U.S.A., contains shallow-water carbonates that have been replaced by dolomite to varying degrees, ranging from partially replaced limestones, to highly porous sucrosic dolostones, to, less commonly, low-porosity dense dolostones. The relationships between dolomitization and porosity and permeability were studied focusing on three 305-m-long cores taken in the City of Daytona Beach. Stable-isotope data from pure dolostones (mean δ 18O = +3.91% V-PDB) indicate dolomite precipitation in Eocene penesaline pore waters, which would be expected to have been at or above saturation with respect to calcite. Nuclear magnetic log-derived porosity and permeability data indicate that dolomitization did not materially change total porosity values at the bed and formation scale, but did result in a general increase in pore size and an associated substantial increase in permeability compared to limestone precursors. Dolomitization differentially affects the porosity and permeability of carbonate strata on the scale of individual crystals, beds, and formations. At the crystal scale, dolomitization occurs in a volume-for-volume manner in which the space occupied by the former porous calcium carbonate is replaced by a solid dolomite crystal with an associated reduction in porosity. Dolomite crystal precipitation was principally responsible for calcite dissolution both at the actual site of dolomite crystal growth and in the adjoining rock mass. Carbonate is passively scavenged from the formation, which results in no significant porosity change at the formation scale. Moldic pores after allochems formed mainly in beds that experienced high degrees of dolomitization, which demonstrates the intimate association of the dolomitization process with carbonate dissolution. The model of force of crystallization-controlled replacement provides a plausible explanation for key observations concerning the dolomitization process in the

Late-stage anhydrite-gypsum-siderite-dolomite-calcite assemblages record the transition from a deep to a shallow hydrothermal system in the Schwarzwald mining district, SW Germany

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Burisch, Mathias; Walter, Benjamin F.; Gerdes, Axel; Lanz, Maximilian; Markl, Gregor

2018-02-01

The majority of hydrothermal vein systems of economic interest occur at relatively shallow crustal levels, although many of them formed at significantly greater depths. Their present position is a consequence of uplift and erosion. Although, many aspects of their formation are well constrained, the temporal chemical evolution of such systems during uplift and erosion is still poorly understood. These vein minerals comprise calcite, dolomite-ankerite, siderite-magnesite, anhydrite and gypsum forming the last gangue assemblages in Jurassic and Tertiary sulphide-fluorite-quartz-barite veins of the Schwarzwald mining district, SW Germany. Mineral textures of samples from nine localities reveal that in these sequences, mineral precipitation follows a recurring pattern: early calcite is followed by anhydrite or gypsum, siderite and/or dolomite. This succession may repeat up to three times. In-situ (LA-ICP-MS) U-Pb age dating of 15 carbonates from three subsequent generations of the late-stage vein assemblage yield robust ages between 20 and 0.6 Ma. Each mineral sequence forms in a distinctive period of about 2-5 Ma. These ages clearly relate these late-stage mineral phases to the youngest geological episode of the Schwarzwald, which is associated with the Cenozoic Rhine Graben rifting and basement uplift. Based on thermodynamic modelling, the formation of the observed mineral assemblages required an deeply sourced Mg-, Fe- and SO4-rich fluid (b), which was episodically mixed with a shallow crustal HCO3-rich fluid (a). As a consequence of fluid mixing, concentrations of Mg, Fe and SO4 temporarily increased and initiated the formation of the observed sulphate-carbonate mineral sequences. This discontinuous large-scale vertical fluid mixing was presumably directly related to episodes of active tectonics associated with the Cenozoic strike-slip regime of the Upper Rhine Graben. Analogously, episodic fluid mixing is a major key in the formation of older (Jurassic to early

Ocean acidification does not affect magnesium composition or dolomite formation in living crustose coralline algae, Porolithon onkodes in an experimental system

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Nash, M. C.; Uthicke, S.; Negri, A. P.; Cantin, N. E.

2015-09-01

There are concerns that Mg-calcite crustose coralline algae (CCA), which are key reef builders on coral reefs, will be most susceptible to increased rates of dissolution under higher pCO2 and ocean acidification. Due to the higher solubility of Mg-calcite, it has been hypothesised that magnesium concentrations in CCA Mg-calcite will decrease as the ocean acidifies, and that this decrease will make their skeletons more chemically stable. In addition to Mg-calcite, CCA Porolithon onkodes, the predominant encrusting species on tropical reefs, can have dolomite (Ca0.5Mg0.5CO3) infilling cell spaces which increases their stability. However, nothing is known about how bio-mineralised dolomite formation responds to higher pCO2. Using P. onkodes grown for 3 and 6 months in tank experiments, we aimed to determine (1) if mol % MgCO3 in new crust and new settlement was affected by increasing CO2 levels (365, 444, 676 and 904 μatm), (2) whether bio-mineralised dolomite formed within these time frames, and (3) if so, whether this was effected by CO2. Our results show that there was no significant effect of CO2 on mol % MgCO3 in any sample set, indicating an absence of a plastic response under a wide range of experimental conditions. Dolomite within the CCA cells formed within 3 months and dolomite abundance did not vary significantly with CO2 treatment. While evidence mounts that climate change will impact many sensitive coral and CCA species, the results from this study indicate that reef-building P. onkodes will continue to form stabilising dolomite infill under near-future acidification conditions, thereby retaining its higher resistance to dissolution.

Effects of the dolomite from Irati formation as additive in a refractory clay used as raw material in Santa Gertrudes ceramic cluster (SP)

International Nuclear Information System (INIS)

Souza, M.H.O.; Gaspar Junior, L.A.; Moreno, M.M.T.

2011-01-01

The effects of addition of carbonates in clays used as floor tiles have been intensively studied, but the focus usually is the pure calcite or calcitic limestone, which has nobler uses in industry, especially for cement production. However, in the important area known as Santa Gertrudes Ceramic Cluster, in Sao Paulo State, occurs mainly the dolomitic limestone, which is little studied as a potential additive which could be used in order to improve the properties of the floor tiles. This work aimed to check out the potentiality of dolomitic limestone as additive in ceramic products, especially floor tiles. Using as ingredients dolomitic limestones and refractory clay collected inside the area of the referred cluster, ceramic bodies were obtained with different dolomitic limestones contents incorporated to the refractory clay, and these ceramic bodies were mineralogically, chemically and physically analyzed. The conclusions are the dolomitic limestone can be particularly useful when incorporated to refractory clays, due to its fluxing properties. (author)

Hydrothermal dolomitization of the Bekhme formation (Upper Cretaceous), Zagros Basin, Kurdistan Region of Iraq: Record of oil migration and degradation

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Mansurbeg, Howri; Morad, Daniel; Othman, Rushdy; Morad, Sadoon; Ceriani, Andrea; Al-Aasm, Ihsan; Kolo, Kamal; Spirov, Pavel; Proust, Jean Noel; Preat, Alain; Koyi, Hemin

2016-07-01

The common presence of oil seepages in dolostones is widespread in Cretaceous carbonate successions of the Kurdistan Region of Iraq. This integrated field, petrographic, chemical, stable C, O and Sr isotopes, and fluid inclusion study aims to link dolomitization to the origin and geochemical evolution of fluids and oil migration in the Upper Cretaceous Bekhme carbonates. Flux of hot basinal (hydrothermal) brines, which is suggested to have occurred during the Zagros Orogeny, resulted in dolomitization and cementation of vugs and fractures by coarse-crystalline saddle dolomite, equant calcite and anhydrite. The saddle dolomite and host dolostones have similar stable isotopic composition and formed prior to oil migration from hot (81-115 °C) basinal NaCl-MgCl2-H2O brines with salinities of 18-22 wt.% NaCl eq. The equant calcite cement, which surrounds and hence postdates saddle dolomite, has precipitated during oil migration from cooler (60-110 °C) NaCl-CaCl2-H2O brines (14-18 wt.% NaCl eq). The yellowish fluorescence color of oil inclusions in the equant calcite indicates that the oil had API gravity of 15-25° composition, which is lighter than present-day oil in the reservoirs (API of 10-17°). This difference in oil composition is attributed to oil degradation by the flux of meteoric water, which is evidenced by the low δ13C values (- 8.5‰ to - 3.9‰ VPDB) as well as by nil salinity and low temperature in fluid inclusions of late columnar calcite cement. This study demonstrates that linking fluid flux history and related diagenesis to the tectonic evolution of the basin provides important clues to the timing of oil migration, degradation and reservoir evolution.

Hydrothermal replacement of calcite by Mg-carbonates

Science.gov (United States)

Jonas, Laura; Mueller, Thomas; Dohmen, Ralf

2014-05-01

The transport of heat and mass through the Earth's crust is coupled to mineral reactions and the exchange of isotopes and elements between different phases. Carbonate minerals are a major constituent of the Earth's crust and play an important role in different physical, chemical and even biological processes. In this experimental study, the element exchange reaction between calcite (CaCO3) and a Mg-rich fluid phase is investigated under hydrothermal conditions. Single crystals of calcite (2x2x2 mm) react with 1 ml of a 1 M MgCl2 solution at 200° C in a Teflon-lined steel autoclave for different times between one day and four weeks. The reaction leads to the formation of a porous reaction front and the pseudomorphic replacement of calcite by dolomite [CaMg(CO3)2] and magnesite (MgCO3). Scanning electron microscopy revealed that the reaction rim consists of small Mg-carbonate rhombs closely attached to each other, suggesting that the replacement reaction takes place by a dissolution-precipitation mechanism. Typically, the observed reaction front can be divided into two different domains. The outer part of the reaction rim, i.e. from the mineral surface in contact to the fluid inwards, consists of magnesite, whereas the inner part of the rim surrounding the unreacted calcite core consists of Ca-rich dolomite. The formation of a porous microstructure that varies in different parts of the reaction rim is a direct result of the large molar volume change induced by the replacement of calcite by magnesite and dolomite. The developing porosity therefore creates fluid pathways that promote the progress of the reaction front towards the unreacted core of the single crystal. Compositional profiles measured perpendicular to the mineral surface across the reactions rims using electron microprobe (EMPA) further revealed a compositional gradient within the reaction rim with regard to the structure-forming elements Mg and Ca. Here, the amount of Mg incorporated in both product

Dolomitization and over-dolomitization in the Vajont limestone (Dolomiti Bellunesi, Italy) controlled by Mesozoic normal faults: a microstructural and diagenesis study

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Cortinovis, Silvia; Swennen, Rudy; Bistacchi, Andrea

2015-04-01

The Vajont Gorge (Dolomiti Bellunesi, Italy) provides spectacular outcrops of Jurassic limestones (Vajont Limestone Formation) in which Mesozoic faults and fracture corridors are continuously exposed. Some of these faults acted as conduits for Mg-enriched hydrothermal fluids resulting in structurally-controlled dolomitization of the limestone. The dolomitization resulted in several dolomite bodies (100-200 m thick and several hundreds of meters along fault strike) that are particularly interesting as reservoir analogues for hydrocarbon, CO2, or water-bearing systems. The dolomitization process occurred after deposition and compaction of the oolitic limestone (dolomitization post-dates a dissolution event that affected the internal parts of the oolites), but before the Alpine contractional deformation. In fact, the meso-structural data collected in the Vajont Gorge allowed the reconstruction of a 3D model showing that the circulation of the dolomitizing fluids into the limestone host rock, but also the late stage of porosity reduction (strong pore filling due to over-dolomitization) were controlled by normal faults and fracture corridors interpreted as Pre-Alpine (Jurassic or Cretaceous). Later on, the influence of Alpine (Tertiary) deformation have been very limited in the studied volume. For instance dolomite veins are sometimes overprinted by bed-inclined stylolites consistent with Alpine shortening axes, but no large Alpine fault is present in the studied outcrops. Cathodoluminescence microscopy allowed recognizing different growth stages saddle dolomite crystals, which point to varying precipitation conditions during three main stages of dolomitization. Dolomite and calcite crystal twinning suggests deformation under increasing temperature conditions, consistent with intracrystalline plasticity deformation mechanisms. The presence of cataclasites composed of hydrothermal dolostone clasts, in turn cemented by dolomite, or of dolomite veins and compaction

Paleoenvironmental and paleohydrochemical conditions of dolomite formation within a saline wetland in arid northwest Australia

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Mather, Caroline C.; Skrzypek, Grzegorz; Dogramaci, Shawan; Grierson, Pauline F.

2018-04-01

Groundwater dolocrete occurring within the Fortescue Marsh, a large inland wetland in the Pilbara region of northwest Australia, has been investigated to provide paleoenvironmental and paleohydrological records and further the understanding of low temperature dolomite formation in terrestrial settings over the Quaternary Period. Two major phases of groundwater dolocrete formation are apparent from the presence of two distinct units of dolocrete, based on differences in depth, δ18O values and mineral composition. Group 1 (G1) occurs at depth 20-65 m b.g.l. (below ground level) and contains stoichiometric dolomite with δ18O values of -4.02-0.71‰. Group 2 (G2) is shallower (0-23 m b.g.l.), occurring close to the current groundwater level, and contains Ca-rich dolomite ± secondary calcite with a comparatively lower range of δ18O values (-7.74 and -6.03‰). Modelled δ18O values of paleogroundwater from which older G1 dolomite precipitated indicated highly saline source water, which had similar stable oxygen isotope compositions to relatively old brine groundwater within the Marsh, developed under a different hydroclimatic regime. The higher δ18O values suggest highly evaporitic conditions occurred at the Marsh, which may have been a playa lake to saline mud flat environment. In contrast, G2 dolomite precipitated from comparatively fresher water, and modelled δ18O values suggested formation from mixing between inflowing fresher groundwater with saline-brine groundwater within the Marsh. The δ18O values of the calcite indicates formation from brackish to saline groundwater, which suggests this process may be associated with coeval gypsum dissolution. In contrast to the modern hydrology of the Marsh, which is surface water dependent and driven by a flood and drought regime, past conditions conducive to dolomite precipitation suggest a groundwater dependent system, where shallow groundwaters were influenced by intensive evaporation.

Experimental observation and numerical simulation of permeability changes in dolomite at CO2 sequestration conditions

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Tutolo, B. M.; Luhmann, A. J.; Kong, X.; Saar, M. O.; Seyfried, W. E.

2013-12-01

mineral, fluid, and aqueous species equations of state into its structure. Phase equilibria calculations indicate that fluids traveling away from the depressed temperature zone near the injection well may exsolve and precipitate up to 200 cc CO2, 1.45 cc dolomite, and 2.3 cc calcite, per kg, but we use the reactive transport simulator to place more realistic limits on these calculations. The simulations show that thermally-induced CO2 exsolution creates velocity gradients within the modeled domain, leading to increased velocities at lower pressure due to the increasingly gas-like density of CO2. Because dolomite precipitation kinetics strongly depend on temperature, modeled dolomite precipitation effectively concentrates within high temperature regions, while calcite precipitation is predicted to occur over a broader range. Additionally, because the molar volume of dolomite is almost double that of calcite, transporting a low temperature, dolomite-saturated fluid across a thermal gradient can lead to more substantial pore space clogging. We conclude that injecting cool CO2 into geothermally warm reservoirs may substantially alter formation porosity, permeability, and injectivity, and can result in favorable conditions for permanent storage of CO2 as a solid carbonate phase.

DOLOMITE THERMAL-DECOMPOSITION MACROKINETIC MODELS FOR EVALUATION OF THE GASGENERATORS SORBENT SYSTEMS

Directory of Open Access Journals (Sweden)

K. V. Dobrego

2015-01-01

Full Text Available Employing dolomite in the capacity of a sorbent for generator gas purification is of considerable interest nowadays, as it is the impurity of generator gas that causes the major problem for creating cheep and effective co-generator plants. Designing gas purification systems employs simple but physically adequate macrokinetic models of dolomite thermal decomposition.  The  paper  analyzes  peculiarities  of  several  contemporaneous  models  of  dolomite and calcite thermal decomposition and infers on reasonable practicality for creating compact engineering dolomite-decomposition macrokinetic models and universal techniques of these models parameter reconstruction for specific dolomite samples. Such technics can be founded on thermogravimetric data and standard approximation error minimizing algorithms.The author assumes that CO2  evacuation from the reaction zone within the particle may proceed by diffusion mechanism and/or by the Darcy filtration and indicates that functional dependence of the thermal-decomposition rate from the particle sizes and the temperature differs for the specified mechanisms. The paper formulates four macrokinetic models whose correspondence verification is grounded on the experimental data. The author concludes that further work in this direction should proceed with the dolomite samples investigation and selecting the best approximation model describing experimental data in wide range of temperatures, warming up rates and the particle sizes.

Chabazite and dolomite formation in a dolocrete profile: An example of a complex alkaline paragenesis in Lanzarote, Canary Islands

Science.gov (United States)

Alonso-Zarza, Ana M.; Bustamante, Leticia; Huerta, Pedro; Rodríguez-Berriguete, Álvaro; Huertas, María José

2016-05-01

This paper studies the weathering and soil formation processes operating on detrital sediments containing alkaline volcanic rock fragments of the Mirador del Río dolocrete profile. The profile consists of a lower horizon of removilised weathered basalts, an intermediate red sandy mudstones horizon with irregular carbonate layers and a topmost horizon of amalgamated carbonate layers with root traces. Formation occurred in arid to semiarid climates, giving place to a complex mineralogical association, including Mg-carbonates and chabazite, rarely described in cal/dolocretes profiles. Initial vadose weathering processes occurred in the basalts and in directly overlying detrital sediments, producing (Stage 1) red-smectites and dolomicrite. Dominant phreatic (Stage 2) conditions allowed precipitation of coarse-zoned dolomite and chabazite filling porosities. In Stages 3 and 4, mostly pedogenic, biogenic processes played an important role in dolomite and calcite accumulation in the profile. Overall evolution of the profile and its mineralogical association involved initial processes dominated by alteration of host rock, to provide silica and Mg-rich alkaline waters, suitable for chabazite and dolomite formation, without a previous carbonate phase. Dolomite formed both abiogenically and biogenically, but without a previous carbonate precursor and in the absence of evaporites. Dominance of calcite towards the profile top is the result of Mg/Ca decrease in the interstitial meteoric waters due to decreased supply of Mg from weathering, and increased supply of Ca in aeolian dust. Meteoric origin of the water is confirmed by C and O isotope values, which also indicate lack of deep sourced CO2. The dolocrete studied and its complex mineral association reveal the complex interactions that occur at surface during weathering and pedogenesis of basalt-sourced rocks.

Geothermometry obtained from the calcite twin and fluid inclusions in barite (Irankuh Pb-Zn deposit, Southwest of Isfahan)

OpenAIRE

Alijan Aftabi; Hengameh Hosseini-Dinani

2017-01-01

The Irankuh mining district is located 20 km southwest of Isfahan and is geologically situated in Sanandaj - Sirjan zone and the lower Cretaceous sequence of Isfahan-Malayer ore mineralization area. The ore minerals are emplaced in the faulted contact of Jurassic shale and Cretaceous carbonates and include pyrite, galena, sphalerite, calcite, barite, dolomite, quartz as well as minor marcasite, smithsonite, cerussite, gypsum, malachite, hematite and goethite. The mineralization is mainly occu...

Subsurface example of a dolomitized middle Guadalupian (Permian) reef from west Texas

Energy Technology Data Exchange (ETDEWEB)

Longacre, S.A.

1983-01-01

A middle Guadalupian organic buildup was cored in the North McElroy Unit (NMU No. 3713 well) in Upton County, W. Texas. Fusulinid control indicates the buildup is equivalent to the Goat Seep reef that crops out in the Guadalupe Mt. The organic buildup at North McElroy consists of boundstones and associated flank grainstones. The reef biota is dominated by ramose and encrusting bryozoans, numerous types of calcareous sponges, the problematic encrusting organism Tubiphytes, encrusting algae, crinoids, brachiopods, and trilobites. Among the more significant aspects of diagenesis are mechanical degradation and biologic degradation, leaching, gypsum-anhydrite transformations, cementation, replacement of all calcite by dolomite, cementation and replacement by baroque dolomite, fracturing, and replacement of carbonate by anhydrite. 17 references.

Characteristics of a calcite "limestone"-marble from Macedonia, used as flux material

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Hristova E.

2003-01-01

Full Text Available The phase characteristics of calcite "limestone"-marble from Banjany area village (near Skopje, Macedonia were examined by means of XRD, SEM microscope in polarizing and reflected lights, chemical, DT/TG-analyses. It was concluded as follows: - calcite (CaCO3 is a major mineral component (cca 80-90 % prevailing in the marble over the other minerals - dolomite is generally of minor importance (cca 10-20 % in the rock - quartz, micas graphite, pyrite represent typical accessories. As result of the mentioned phase characteristics, this raw materials was for a long time (more than 30 years used as flux in the iron and steel metallurgy in Macedonia.

A urolith of biogenic dolomite - another clue in the dolomite mystery

Science.gov (United States)

Mansfield, Charles F.

1980-06-01

A male Dalmatian, Canis familiaris, produced uroliths of almost pure dolomite, 3-8 mm across, in his urinary bladder in less than 8 months at 38°C and about 1 atm. The X-ray diffractogram identified the predominant mineral as dolomite, and the sharp (01.5) peak showed it is ordered dolomite, not the disordered form, protodolomite. Geochemically and biologically plausible causes include (1) renal, respiratory, or metabolic alkalosis, (2) infection by urease-producing (urea-splitting) fungi or bacteria and (3) infection by uric acid-fermenting bacteria. Hematological, bacteriological, urological and geochemical considerations most strongly implicate infection by either anaerobic, urease-producing bacteria or anaerobic, uric acid-fermenting bacteria. The physical and chemical conditions of this urinary system more closely approximate modern and inferred ancient carbonate depositional settings than most previous laboratory experiments, especially in terms of temperature, pressure, total salinity and, possibly, biota. The presence of urease-producing and/or uric acid-fermenting bacteria in urea- and/or acid-containing sediment, such as fecal pellets and algal mats, could promote formation of authigenic dolomite or other carbonates.

Ferroan dolomites in Miocene sediments of the Xisha Islands and their genetic model

Science.gov (United States)

Xu, Hong; Zhang, Weiwei; Wei, Kai; He, Qingkun; Jiang, Yunshui; Xu, Tingting; Jiang, Xuejun; Yan, Guijing; Song, Hongying; Wang, Jianghai

2018-01-01

Carbonate rocks are important reservoirs for global petroleum exploration. The largest oilfield in the South China Sea, Liuhua 11-1, is distributed in the massive carbonate reef area of the Zhujiang (Pearl) River Mouth Basin. Previous studies showed that one 802.17-m-long core from well Xichen-1 in the South China Sea mainly consisted of white and light gray-white organic reefs. Recently, a Miocene whole core (161.9 m long) of well Xiyong-2, near well Xichen-1, was found to contain six layers of yellowish brown, light yellowish gray, iron black, or light yellowish gray-white organic reefs. Scanning electron microscope images of these layers reveal a typical ferroan dolomite rich in Fe (up to 29%), with the high concentrations of Mn, Cu, W, Zn, Cr, Ni, and Co. Systematic X-ray powder diffraction analysis yields a 1.9-6.1 match in phase ratio with ankerite, 5.4-26.9 with dolomite, and zero with calcite, which indicate that the samples can be classified as ferroan dolomite. The iron and heavy metals are inferred to be originated from multiple volcanic eruptions of Gaojianshi Island in the Dongdao Atoll during the middle-late Miocene. These elements were dissolved in seawater, likely as a sol, and carried to Yongxing Island in the Xuande Atoll by sea currents and tides enhanced by prevailing winds, and deposited as a part of the sedimentation process in the study area. The ferroan dolomite has Sr content of (125-285)×10-6, which is lower than the accepted Sr boundary value of dolomite. This finding suggests that dolomitization occurred during large-scale global glacial regression in the late Miocene. The isolated Xisha carbonate platform, exposed to air, underwent freshwater leaching and dolomitization induced by mixed water, and caused the extensive Fe-Mg exchange along the organic reef profile to form ankerite and ferroan dolomite. These results may help to understand paleoceanographic environmental changes in the South China Sea during the Miocene.

Fabric Preserving and Fabric Destroying Dolomitization: A case of Seawater Dolomitization

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Alham Jassim Al-Langawi

2006-06-01

Full Text Available This study is based on field, petrographic and geochemical investigations of Hajar Supergroup autochthonous rocks: Ruus Al Jibal Group- Musandam Peninsula, and Akhdar Group- Jebel Akhdar, Oman and U.A.E., and para-autochthonous Maqam Formation-Sumeini Group-Jebel Sumeini-U.A.E.  Petrographic evidence indicates that the rocks were deposited in a shallow marine shelf environment, particularly tidal flat, lagoon, reef, back-reef and shoal environments that were part of the Arabian Platform during Permian and Triassic times. However, they are almost entirely dolomitized and the rocks show different petrographic features ranging from perfect preservation of original texture by mimetic dolomitization to complete obliteration and destruction of the original limestones giving rise to inequicrystalline and equicrystalline fabrics.  Dolomites analyzed by geochemical methods were categorized on the basis of textural variations; crystal size, shape and impurity or inclusion distribution within crystals, and whether these crystals are found as rock forming (replacive or cements. The dolomites display variations in stoichiometry, ordering and trace element concentrations indicating differences in dolomitizing fluid chemistry and recrystallization stages that prevailed through time. It indicates also that although dolomitization is pervasive, dolomites are petrographically and chemically immature. All the petrographic and geochemical evidence strongly indicates seawater and/or mixing zone dolomitization which may have been initiated soon after deposition of the host sediments.  Rocks showing preservation of allochems as well as the marine cements by mimetic dolomite crystals, suggest that dolomitization was early (at shallow depths with very active marine-water circulation and occurred in a relatively short time.  Evidence from crystalline dolomites indicates several crystallization events at shallow burial depths, under marine waters modified by increased

Examining the interplay of climate and low amplitude sea-level change on the distribution and volume of massive dolomitization: Zebbag Formation, Cretaceous, Southern Tunisia

DEFF Research Database (Denmark)

Newport, Richard; Hollis, Cathy; Bodin, Stéphane

2017-01-01

During the Cretaceous, a humid global climate, calcitic seas, high relative sea-level and low amplitude changes in relative sea-level largely prevented large-scale dolomitization in many carbonate successions. However, the well-exposed shallow-water carbonate sediments of the Upper Albian–Lower T...

Review of Dolomite as Precursor of Geopolymer Materials

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Azimi E.A.

2016-01-01

Full Text Available Geopolymer is an environmentally friendly cementitious binder that does not require the existence of ordinary Portland cement (OPC. Geopolymer has many excellent advantages, including high early strength, low shrinkage, good thermal resistance and good chemical resistance. Previous commonly used materials include fly ash, clay and slag. The used of dolomite as precursor material in geopolymer field is still new and at the early stage of study. Only a few researchers have done studies on dolomite in geopolymer. Dolomite (CaMg(CO32 is abundant and generally inexpensive natural minerals. The possible use of these bulk calcium carbonate materials in improving the mechanical properties of geopolymers will therefore be of great interest. This paper summarizes some research outcomes on dolomite in geopolymer along with the potential of dolomite as geopolymer composites.

SEDIMENTOLOGY, MINERALOGY AND ORIGIN OF THE FIRST DISCOVER MAGNESITE-DOLOMITE BELT IN MA'RIB DISTRICT, SW ARABIAN PENINSULA

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Sa’ad Zeki A.kader AL-MASHAIKIE

2016-10-01

Full Text Available Magnesite mineralization of high purity was discovered and described herein for the first time from metamorphosed folded belt from Al-Thanyiah locality in Rub’Al-Khali sector, 360 km east of Sana’a City, northwest Yemen. The magnesite-metamorphic belt, belonging to the Precambrian/Neoproterozoic age? comprises thrust belt, which trends generally N-S direction.Magnesite mineralization was identified in an extended carbonate-metamorphic belt for several tens of kilometers cf. 31 km and occurred in association with 8 stratigraphic units. The thicknesses of pure magnesite bearing units are variable and ranges from 20 to 60 m. associated with dark green chlorite-schist with intersecting huge ultrabasic intrusions.Geochemical, mineralogical and petrographic analysis show that the magnesite concentrations in the stratigraphic units are ranging from 78% up to high purity of 99.6% cf. 35 to 48.9% MgO, with minor dolomite and calcite respectively. Little to rare content of talc and brucite were also recognized. Two thick, productive and high purity magnesite beds, the first is of 40 m thick and the second is 60 m in thickness, which reveals more than 95% MgCO3 and considered to be economic. The suggested origin of the magnesite mineralization is coming from high stress of regional metamorphism associated with ultramafic intrusions cf. amphibolite and harzburgite associated with diagenetic solutions rich in Mg2+, associated with the heat of magma. The alteration of dolomite to magnesite was formed by multiple phases to transform calcite and/or dolomite to magnesite.

Geothermometry obtained from the calcite twin and fluid inclusions in barite (Irankuh Pb-Zn deposit, Southwest of Isfahan

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Alijan Aftabi

2017-03-01

Full Text Available The Irankuh mining district is located 20 km southwest of Isfahan and is geologically situated in Sanandaj - Sirjan zone and the lower Cretaceous sequence of Isfahan-Malayer ore mineralization area. The ore minerals are emplaced in the faulted contact of Jurassic shale and Cretaceous carbonates and include pyrite, galena, sphalerite, calcite, barite, dolomite, quartz as well as minor marcasite, smithsonite, cerussite, gypsum, malachite, hematite and goethite. The mineralization is mainly occurred as hydrothermal veins and veinlets associated with fractures and faults, suggesting the deposit is likely to be of epigenetic type. A comparison between geothermometric results obtained from calcite twins and fluid inclusions showed a similar temperature range for the mineralization (less than 170ºc. Fluid inclusion studies indicate the temperature, salinity and density ranges of 80-166ºc, 5.39-20.94 wt.% NaCl and 0.95-1.12, respectively. The obtained data share many similarities with those of the MVT deposits

Strontium isotopic stratigraphy utilizing authigenic dolomites in hemipelagic sediments

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Baker, P.A. (Duke Univ., Durham, NC (USA)); Kastner, M. (Scripps Institute of Oceanography, La Jolla, CA (USA)); Elderfield, H. (Univ. of Cambridge (England))

1990-05-01

Authigenic dolomites commonly occur in organic-rich, continental margin marine sediments. These dolomites play a key role in the age dating of stratigraphic sections. The dolomites often are the only lithology amenable to paleomagnetic stratigraphy; they preserve siliceous microfossils against diagenetic; recrystallization, and provide useful strontium isotopic stratigraphic ages. Several potential sources of error frequently are unique to the use of authigenic dolomites in the strontium isotope methods. (1) The dolomites occur as cements of the host lithology, hence, they are not a pure phase. Potentially important contaminants during analysis include gypsum clay minerals, feldspars, and iron and manganese oxides. Strontium may occur as a structural substituent ion in these minerals or as a surface-adsorbed ion. Various leaching techniques have been tested to isolate dolomitic strontium. Purer dolomites and strontium-enriched dolomites often can be selected to ease these problems. (2) The dolomites form after the deposition of the host sediment, therefore, they record the diagenetic age not the depositional age. The stable isotopic composition of the dolomites can aid in selection of early formed samples. (3) The dolomites record pore-water strontium isotope compositions, not seawater isotopic compositions. This problem is also minimized by choosing dolomites formed near the sediment-water interface. (4) The dolomites formed near the sediment-water interface originated as rotodolomites and undergo subsequent burial diagenesis, creating a potential for later strontium isotope exchange. This problem is minimized by selecting fresh samples from the interior of nearly impermeable beds and nodules. Results from the Miocene Monterey Formation of California and from the Eocene through Pliocene Pisco basin of Peru show that authigenic dolomites can provide useful strontium isotopic age estimates.

The magnesium isotope (δ26Mg) signature of dolomites

Science.gov (United States)

Geske, A.; Goldstein, R. H.; Mavromatis, V.; Richter, D. K.; Buhl, D.; Kluge, T.; John, C. M.; Immenhauser, A.

2015-01-01

Dolomite precipitation models and kinetics are debated and complicated due to the complex and temporally fluctuating fluid chemistry and different diagenetic environments. Using well-established isotope systems (δ18O, δ13C, 87Sr/86Sr), fluid inclusions and elemental data, as well as a detailed sedimentological and petrographic data set, we established the precipitation environment and subsequent diagenetic pathways of a series of Proterozoic to Pleistocene syn-depositional marine evaporative (sabkha) dolomites, syn-depositional non-marine evaporative (lacustrine and palustrine) dolomites, altered marine ("mixing zone") dolomites and late diagenetic hydrothermal dolomites. These data form the prerequisite for a systematic investigation of dolomite magnesium isotope ratios (δ26Mgdol). Dolomite δ26Mg ratios documented here range, from -2.49‰ to -0.45‰ (δ26Mgmean = -1.75 ± 1.08‰, n = 42). The isotopically most depleted end member is represented by earliest diagenetic marine evaporative sabkha dolomites (-2.11 ± 0.54‰ 2σ, n = 14). In comparing ancient compositions to modern ones, some of the variation is probably due to alteration. Altered marine (-1.41 ± 0.64‰ 2σ, n = 4), and earliest diagenetic lacustrine and palustrine dolomites (-1.25 ± 0.86‰ 2σ, n = 14) are less negative than sabkha dolomites but not distinct in composition. Various hydrothermal dolomites are characterized by a comparatively wide range of δ26Mg ratios, with values of -1.44 ± 1.33‰ (2σ, n = 10). By using fluid inclusion data and clumped isotope thermometry (Δ47) to represent temperature of precipitation for hydrothermal dolomites, there is no correlation between fluid temperature (∼100 to 180 °C) and dolomite Mg isotope signature (R2 = 0.14); nor is there a correlation between δ26Mgdol and δ18Odol. Magnesium-isotope values of different dolomite types are affected by a complex array of different Mg sources and sinks, dissolution/precipitation and non

The Ranero Hydrothermal Dolomites (Albian, Karrantza Valley, Northwest Spain: Implications on Conceptual Dolomite Models Les dolomies hydrothermales de Ranero (Albien, vallée de la Karrantza, nord-ouest de l’Espagne : conséquences sur les modèles génétiques

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Nader F.H.

2012-02-01

Full Text Available Field characteristics, petrographic and geochemical signatures, as well as some petrophysical aspects of fault-related dolomite bodies in the Ranero area (Karrantza Valley, NW Spain are presented in this paper. These dolomite bodies are hosted by Albian slope to platform carbonates, which were deposited in the Basque-Cantabrian Basin. Replacive and void-filling dolomite phases – postdating palaeo- and hypogene karstification – are interpreted to have originated from hydrothermal fluid pulses, and are spatially related with faults and fractures. Hydrothermal calcite cements pre- and postdate dolomitization. Mineralogical and geochemical investigations (XRD, ICP-MS/OES, XRF, stable and Sr isotopes helped in distinguishing various dolomite and calcite phases. Dolomite phases can be grouped into ferroan (early and non-ferroan (late. Dolomites are generally stoichiometric and exhibit a broad range of depleted δ18O values (–18.7 to –10.5‰ V-PDB, which advocate for multiphase dolomitization and/or recrystallization at relatively high temperatures (150-200°C. The observation that bed-parallel stylolites pre- and post-date dolomites suggests that dolomitization occurred during the Late Albian regional tectonic activity and related fluid expulsions. Based on carbonate chemistry, authigenic silicate chemistry and replacement relationships, two contrasting types of dolomitizing fluids are inferred. Both arguably may have initiated as sulphatedominated brines and/or basin compactional fluids, but they seemingly undergo sulphate reduction in contact with host rocks of contrasting compositions (Fe-rich silicate vs Fe-poor carbonate thus evolving either to acidic and ferroan (limestone replacive or to neutral, Fe-poor and sulfidic (Fe-dolomite replacive. Fluid drives are not well constrained by our data, but both fluid types are focused along major faults that cross cut the platform edge and are associated with diapir tectonics. Les modalités de

Dolomitic lime containing hydraulic additive

International Nuclear Information System (INIS)

Lagzdina, S.; Sedmalis, U.; Bidermanis, L.; Liepins, J.; Grosvalds, I.

1997-01-01

To obtain qualitative dolomitic lime the optimum calcination temperature of dolomite containing about 9 % of clayey substances is 900 deg C. The mechanical strength of dolomitic lime containing 30 % of brick waste additive after 6-9 months of hardening is 1.4-1.5 times higher than that of samples without hydraulic additive, for calcium lime - 2.2-2.6 times higher. Generally the mechanical strength of dolomitic lime is higher than that one of calcium lime. It can be explained by the active role of MgO in the hydration and hardening processes of dolomitic lime. Xray diffraction phase analysis was performed by X-ray diffractometer DPON-3M with Cu-K α emission filter

Petrography and diagensis of Padeha Formation sandstones (Lower-Middle Devonian at Bujhan section, Binalud Basin, NE Iran

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Mehdi Reza Poursoltani

2016-12-01

Conclusion: Based on petrological and geochemical studies, minor diagenetic events in the eodiagenetic stage include cementation (calcite, dolomite and iron oxide and rarely fracturing. Mesodiagenetic events were dominated by cementation (silica, dolomite, calcite, iron oxide components, clay minerals, compaction, intra-grain microfractures, alteration of unstable clasts, dissolution and replacement, pressure solution, and rarely formation of apatite. Minor telodiagenetic events include dissolution and cementation (dolomite, ankerite, siderite, iron oxide and rarely kaolinite. The bulk of the porosity is secondary, with an average of 4.7%, which is the result of dissolution and fractures

Diagenetic conditions of fibrous calcite vein formation in black shales: Petrographic, chemical and isotopic evidence

Energy Technology Data Exchange (ETDEWEB)

Al-Aasm, I.S.; Muir, I. (Imperial Oil Resources, Calgary, AB (Canada)); Morad, S. (Windsor Univ., ON (Canada))

1992-03-01

Antiaxial fibrous calcite veins 2-6 cm thick outcrop parallel to bedding in the Bluefish Member of the Middle Devonian Hare Indian Formation in the Norman Wells area of the Northwest Territories. The Bluefish Member consists of dark brown to black laminated shales with total organic matter content in the 1.8-8.0 wt % range. The basal part of the Member, characterized by the presence of low diversity macrofossils, was deposited under anaerobic conditions on top of the drowned Hume carbonate platform. The pattern of incorporation of host-shale fragments and tiny inclusions into the fibrous calcite indicates repeated episodes of vein opening and sealing. The [delta][sup 13]C values and the low Mn and Fe contents indicate a dominantly marine source of carbonate ions was related to the dissolution of metastable skeletal carbonates in the host shales. The [delta][sup 18]O values suggest precipitation at 30-50[degree]C and burial depths of tens to hundreds of meters. The formation of finely crystalline non-stoichiometric Ca-rich dolomite disseminated in the shale inclusions occurred subsequent to the emplacement of fibrous calcite veins under elevated burial temperatures. 54 refs., 8 figs., 3 tabs.

Shock-induced devolatilization of calcite

Science.gov (United States)

Boslough, M. B.; Ahrens, T. J.; Vizgirda, J.; Becker, R. H.; Epstein, S.

1982-01-01

Experimental measurements of the release adiabats by Vizgirda (1981) indicate that substantial vaporization takes place upon release from shock pressures of 37 GPa for calcite and 14 GPa for aragonite. The present investigation includes the first controlled partial vaporization experiments on calcite. The experiments were conducted to test the predictions of the release adiabat experiments. The quantities of the gaseous species produced from shocked calcite and their carbon and oxygen isotopic compositions were determined, and the shock-induced effect on the Mn(2+) electron spin resonance spectrum in the shock-recovered calcite was observed. On the basis of the obtained results, it is concluded that shock stresses at the 17-18 GPa level give rise to volatilization of 0.03-0.3 (mole) percent of calcite to CO2 and CO. The devolatilization of calcite occurs at low pressure at significantly lower entropy densities than predicted on the basis of thermodynamic continuum models.

Dolomite decomposition under CO2

International Nuclear Information System (INIS)

Guerfa, F.; Bensouici, F.; Barama, S.E.; Harabi, A.; Achour, S.

2004-01-01

Full text.Dolomite (MgCa (CO 3 ) 2 is one of the most abundant mineral species on the surface of the planet, it occurs in sedimentary rocks. MgO, CaO and Doloma (Phase mixture of MgO and CaO, obtained from the mineral dolomite) based materials are attractive steel-making refractories because of their potential cost effectiveness and world wide abundance more recently, MgO is also used as protective layers in plasma screen manufacture ceel. The crystal structure of dolomite was determined as rhombohedral carbonates, they are layers of Mg +2 and layers of Ca +2 ions. It dissociates depending on the temperature variations according to the following reactions: MgCa (CO 3 ) 2 → MgO + CaO + 2CO 2 .....MgCa (CO 3 ) 2 → MgO + Ca + CaCO 3 + CO 2 .....This latter reaction may be considered as a first step for MgO production. Differential thermal analysis (DTA) are used to control dolomite decomposition and the X-Ray Diffraction (XRD) was used to elucidate thermal decomposition of dolomite according to the reaction. That required samples were heated to specific temperature and holding times. The average particle size of used dolomite powders is 0.3 mm, as where, the heating temperature was 700 degree celsius, using various holding times (90 and 120 minutes). Under CO 2 dolomite decomposed directly to CaCO 3 accompanied by the formation of MgO, no evidence was offered for the MgO formation of either CaO or MgCO 3 , under air, simultaneous formation of CaCO 3 , CaO and accompanied dolomite decomposition

Neutralization of sulfuric acid solutions by calcite dissolution and the application to anoxic limestone drain design

International Nuclear Information System (INIS)

Huminicki, Danielle M.C.; Rimstidt, J. Donald

2008-01-01

Batch reactor (BR) experiments were conducted to measure the effect of hydrodynamics and gypsum coatings on calcite neutralization rates. A factorial array of BR experiments measured the H + concentration change by calcite dissolution over a pH range of 1.5-3.5 and Na 2 SO 4 concentrations of 0-1 M. The rate of H + concentration change with time was determined by numerical differentiation of H + concentration versus time. Regression modeling showed that for uncoated calcite, rates are only significantly affected by pH, r=-10 -2.32 a H + 0.76 . Whereas, for calcite coated with gypsum only time had a significant effect on calcite dissolution rates, r = -10 -1.96 t -0.53 . Because transport-limited dissolution rates for uncoated calcite are a function of the pH and Reynolds number, a model was developed to express the effects of these two variables on the rate of H + consumption for a solution with a Darcy velocity, q, through a porous medium with a particle radius, r p , such that r ' =1.08x10 -3 q 0.31 r p -0.69 m H + 0.87 . This equation was integrated via a numerical model to simulate the performance of an idealized anoxic limestone drain (ALD). This model predicts the pH and alkalinity change along the length of an ALD. The model shows that the efficiency of an ALD is greater when the Darcy velocity is low and the particle radius is small. In addition, the growth of gypsum coatings causes the rate of H + neutralization to decline as the square root of time as they form and block the H + transport to the calcite surface. Supersaturation with respect to gypsum, leading to coating formation, can be avoided by diluting the ALD feed solution or by replacing limestone with dolomite

Hydrothermal Dolomites in the Early Albian (Cretaceous Platform Carbonates (NW Spain: Nature and Origin of Dolomites and Dolomitising Fluids Dolomies hydrothermales présentes dans les carbonates de la plate-forme albienne précoce (Crétacé; NO de l’Espagne : nature et origine des dolomies et des fluides dolomitisants

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Shah M.M.

2012-02-01

Full Text Available This study documents the temporal and lateral variation in petrographic and geochemical signatures of fault-related dolomite bodies in the Ranero and El-Moro areas (Karrantza valley, Cantabrian mountains; NW Spain. These dolomite bodies are hosted in Albian carbonates, which were deposited in the Basque-Cantabrian Basin as a result of an intense rift-related subsidence with associated faulting along various orientations. Fluid circulations generated replacive and cement dolomites, paragenetically followed by various calcite cements. Petrography, mineralogical and geochemical investigations (XRD, ICP, XRF, stable and Sr isotopes helped in distinguishing hydrothermal stages. Two major dolomite facies were observed according to their Fe-content. Early dolomites are ferroan and replace limestone more significantly than the later, non ferroan dolomites. Dolomites are generally stoichiometric (49.76 to 51.59 M% CaCO3 and exhibit a broad range of depleted δ18O values (–18.7 to –10.5‰ V-PDB, which may indicate multiphase dolomitisation and/or different degrees of recrystallisation. Decreasing δ18O values correlate with decreasing Fe content in dolomites. In the Ranero area, dolomites show less slightly depleted δ13C values (–0.15 to +2.13‰ V-PDB relative to the host limestone δ13C signature, while these values are substantially more depleted in El-Moro area (down to –2.18‰ V-PDB. Hydrothermal calcites predating dolomitisation show less depleted δ18O values (–14.15 to –12.1‰ V-PDB than postdolomitisation calcite (–18.1‰ V-PDB. Sr isotope data suggest that the fluids interacted with siliciclastic lithologies (sandstone, shale. The dolomite fabric is variably altered through dedolomitisation and cataclastic deformation. Dolomitisation occurred in at least two main episodes. A first episode of pervasive ferroan dolomitisation probably resulted from compactional dewatering of basinal fluids from the nearby Basque trough and

Meteoric calcite cementation: diagenetic response to relative fall in sea-level and effect on porosity and permeability, Las Negras area, southeastern Spain

Science.gov (United States)

Li, Zhaoqi; Goldstein, Robert H.; Franseen, Evan K.

2017-03-01

A dolomitized Upper Miocene carbonate system in southeast Spain contains extensive upper and lower zones of calcite cementation that cut across the stratigraphy. Cement textures including isopachous and circumgranular, which are consistent with phreatic-zone cementation. Cements in the upper cemented zone are non-luminescent, whereas those in the lower cemented zone exhibit multiple bands of luminescent and non-luminescent cements. In the upper cemented zone, isotopic data show two meteoric calcite lines (MCL) with mean δ18O at - 5.1‰ and - 5.8‰ VPDB, whereas no clear MCL is defined in the lower cemented zone where mean δ18O for calcite cement is at - 6.7‰ VPDB. δ13C values in both cement zones are predominantly negative, ranging from - 10 to + 2‰ VPDB, suggestive of carbon from soil gas or decayed organics. Measurements of Tm ice in primary fluid inclusions yield a mode of 0.0 °C in both zones, indicating calcite cementation from fresh water. These two zones define the positions of two different paleo-water tables that formed during a relative sea-level fall and erosional downcutting during the Plio-Pleistocene. The upper cemented zone pre-dated the lower cemented zone on the basis of known relative sea-level history. Meteoric calcite cementation reduced porosity and permeability, but measured values are inconsistent with simple filling of open pore space. Each texture, boundstone, grainstone, packstone, wackestone, produces a different relationship between percent calcite cement and porosity/permeability. Distribution of cements may be predictable on the basis of known sea-level history, and the effect of the cementation can be incorporated into subsurface geomodels by defining surfaces of rock boundaries that separate cemented zones from uncemented zones, and applying texture-specific relationships among cementation, porosity and permeability.

Authigenic carbonates in sediments from the Gulf of Mexico

International Nuclear Information System (INIS)

Botz, R.; Brooks, J.M.

1988-01-01

The carbon isotopic composition of diagenetic dolomite and calcite in some sediments of the Gulf of Mexico varies between 'normal-marine' (δ 13 C ca. 0per mille) and - 14.6per mille which suggests that biogenic CO 2 contributed to the carbonate formations. The δ 18 O values of dolomite and coexisting calcite are very similar but variable down-core. Dolomite and calcite precipitated early from pore water where SO 4 2- was not reduced. However, during (and after?) SO 4 2- reduction dolomite and calcite still formed and there are at least two generations of carbonate minerals present. (orig.)

An Exercise on Calibration: DRIFTS Study of Binary Mixtures of Calcite and Dolomite with Partially Overlapping Spectral Features

Science.gov (United States)

De Lorenzi Pezzolo, Alessandra

2013-01-01

Unlike most spectroscopic calibrations that are based on the study of well-separated features ascribable to the different components, this laboratory experience is especially designed to exploit spectral features that are nearly overlapping. The investigated system consists of a binary mixture of two commonly occurring minerals, calcite and…

Chemical composition and strength of dolomite geopolymer composites

Science.gov (United States)

Aizat, E. A.; Al Bakri, A. M. M.; Liew, Y. M.; Heah, C. Y.

2017-09-01

The chemical composition of dolomite and the compressive strength of dolomite geopolymer composites were studied. The both composites prepared with mechanical mixer manufactured by with rotor speed of 350 rpm and curing in the oven for 24 hours at 80˚C. XRF analysis showThe dolomite raw materials contain fewer amounts of Si and Al but high Ca in its composition. Dolomite geopolymer composites with 20M of NaOH shows greater and optimum compressive strength compared to dolomite geopolymer with other NaOH molarity. This indicated better interaction of dolomite raw material and alkaline activator need high molarity of NaOH in order to increase the reactivity of dolomite.

Analysis of the Erosion Law of Karst Groundwater Using Hydrogeochemical Theory in Liulin Spring Area, North China

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Xiuqing Zheng

2018-05-01

Full Text Available The comprehensive geological, hydrogeological and hydrogeochemical model of the Liulin karstic spring area in the eastern limb of the Ordos syncline was established by a combination of chemical thermodynamics, chemical kinetics and hydrogeology. The study area was divided into four zones based on the saturation indices of calcite, dolomite and gypsum, which were computed by the groundwater-chemical simulation software PHREEQC (a computer program for speciation, batch-reaction, one-dimensional transport, and inverse geochemical calculations, with consideration of the geological and hydrogeological conditions and hydro-geochemical reactions. The weight and volume modulus of carbonate rocks and sulphate rocks in each zone were calculated by the method of correlation analysis to evaluate the dissolution law of karst groundwater. The results showed that in the zone I (saturation index of calcite βc ≤ 1 the dissolution of calcite was the major geochemical reaction, the weight modulus of calcite was higher than that of dolomite and gypsum, and the pore space generated by the dissolution of calcite was one order of magnitude larger than that of dolomite and gypsum. In zone II (saturation index of calcite βc > 1 to saturation index of dolomite βd ≤ 1 the corrosion moduli were all smaller than that in zone I, the solubility of dolomite and gypsum increased, and calcite reached saturation. The space occupied by the calcite sediment was less than that dissolved by dolomite and gypsum. In zone III (saturation index of dolomite βd > 1 to saturation index of gypsum βg ≤ 1, calcite and dolomite had reached saturation, accompanied by dedolomitization, and the amount of gypsum dissolution increased obviously. The conclusions indicate that the hydrogeochemical environment plays an important role in mineral dissolution.

Weathering of dolomite in industrial environments

International Nuclear Information System (INIS)

Gauri, K.L.; Tambe, S.S.; Caner-Saltik, E.N.

1992-01-01

To the exclusion of other major atmospheric pollutants, sulfur dioxide is mainly responsible for attack upon dolomite. This article characterizes Laurel Dolomite on the basis of composition, texture, and porosity; describes the mechanism of the SO 2 reaction with dolomite; and develops two equations for the prediction of the rate of decay of dolomite. Over a period of 120 yr nearly 3.57 mm surface reduction at protected areas and 0.915 mm surface reduction at unprotected surfaces of a building in Louisville was calculated. However, these values could not be verified because measurement of these quantities in the field cannot be made

Wetting behavior of magnesite and dolomite surfaces

Science.gov (United States)

Gence, Nermin

2006-03-01

Magnesite and dolomite are salt-type minerals that show similar chemical composition and flotation behavior due to same crystal structure, and sparingly soluble nature. The surface properties of minerals play a major role in determining their separation from each other in processes such as flotation. During flotation process, selectivity problem arises between magnesite and associated gangue minerals such as dolomite. There is a close relationship between floatability of minerals and their contact angles. Therefore, surface hydrophobicity of magnesite and dolomite minerals was investigated by contact angle measurements in the absence and presence of flotation reagents. Magnesite and dolomite show hydrophilic properties and they have got a small contact angle (magnesite ˜10.4° and dolomite ˜6.6°) in distilled water in the absence of any surfactant. The contact angle values at the magnesite and dolomite surfaces remained at 9.7°-10.9° in the presence of petroleum sulphonates (R825 and R840) while sodium oleate affected hydrophobicity of magnesite, and the contact angle value increased up to 79°. The contact angle value of 39° at dolomite surface was obtained in the solution of sodium oleate, respectively.

Hydrothermal dolomite reservoir facies in the Sinian Dengying Fm, central Sichuan Basin

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Yuqiang Jiang

2017-07-01

Full Text Available The Upper Sinian Dengying Fm is the focus of natural gas exploration in the central part of the Sichuan Basin (central Sichuan Basin in recent years. Especially, epigenic karstification and its resulted reservoir-seepage spaces have always been the focal points in researches. Based on the petrographic characteristics of drilling cuttings and core samples, and through experimental analysis by using trace elements, isotopes, and cathodoluminescence, the Dengying Fm dolomite was demonstrated to have matrix recrystallized dolomite (MRD, filled saddle dolomite (FSD (the mean homogenization temperature of inclusion: 178.5 °C, high concentrations of Fe & Mn, slightly positive 87Sr/86Sr value and hydrothermal minerals combination (including sphalerite, galena, pyrite, and quartz, etc.. Thus, it was proposed that hydrothermal dolomite reservoir facies (HDRF exist in the Dengying Fm dolomite, in other words, the dolomite reservoir is composed of hydrothermal dissolved pores, intercrystalline pores of hydrothermal origin, hydrothermal caverns and expanded fractures, and was formed due to the reworking of hydrothermal fluid on tight matrix dolomite. Identification marks are presented in terms of petrography and geochemistry so that hydrothermal dolomite reservoir facies can be effectively recognized and identified. It is concluded that the development of hydrothermal dolomite reservoir facies in this area are preliminary controlled by deep and large basement faults and the strength of hydrothermal fluids.

Mechanism for calcite dissolution and its contribution to development of reservoir porosity and permeability in the Kela 2 gas field,Tarim Basin,China

Institute of Scientific and Technical Information of China (English)

2008-01-01

This study is undertaken to understand how calcite precipitation and dissolution contributes to depth-related changes in porosity and permeability of gas-bearing sandstone reservoirs in the Kela 2 gas field of the Tarim Basin, Northwestern China. Sandstone samples and pore water samples are col-lected from well KL201 in the Tarim Basin. Vertical profiles of porosity, permeability, pore water chem-istry, and the relative volume abundance of calcite/dolomite are constructed from 3600 to 4000 m below the ground surface within major oil and gas reservoir rocks. Porosity and permeability values are in-versely correlated with the calcite abundance, indicating that calcite dissolution and precipitation may be controlling porosity and permeability of the reservoir rocks. Pore water chemistry exhibits a sys-tematic variation from the Na2SO4 type at the shallow depth (3600-3630 m), to the NaHCO3 type at the intermediate depth (3630―3695 m),and to the CaCl2 type at the greater depth (3728―3938 m). The geochemical factors that control the calcite solubility include pH, temperature, pressure, Ca2+ concen-tration, the total inorganic carbon concentration (ΣCO2), and the type of pore water. Thermodynamic phase equilibrium and mass conservation laws are applied to calculate the calcite saturation state as a function of a few key parameters. The model calculation illustrates that the calcite solubility is strongly dependent on the chemical composition of pore water, mainly the concentration difference between the total dissolved inorganic carbon and dissolved calcium concentration (i.e., [ΣCO2] -[Ca2+]). In the Na2SO4 water at the shallow depth, this index is close to 0, pore water is near the calcite solubility. Calcite does not dissolve or precipitate in significant quantities. In the NaHCO3 water at the intermedi-ate depth, this index is greater than 0, and pore water is supersaturated with respect to calcite. Massive calcite precipitation was observed at this depth

Impact of diagenesis and low grade metamorphosis on Triassic sabkha dolomite δ26Mg

Science.gov (United States)

Immenhauser, A.; Geske, A.; Richter, D.; Buhl, D.; Niedermayr, A.

2012-12-01

Dolomite is a common rock forming mineral in the geological record but its value as archive of ancient seawater δ26Mg signatures and their variations in time are at present underexplored. Unknown factors include the sensitivity of δ26Mg ratio to processes in the diagenetic and low grade metamorphic domain. Here, we document and discusses the first detailed δ26Mg data set from early diagenetic and burial dolomites. Samples come from the Upper Triassic Hauptdolomit (Dolomia Principale; The Dolomites, Italy) and include coeval dolmicrites that underwent differential burial diagenesis in a temperature range between about 100 and more than 350°C. As indicated by dolmicrite 87/86Sr ratios, sabkha calcian D1 dolomites precipitated from evaporated seawater and stabilized at an early diagenetic stage to D2 dolomites analysed here. With increasing burial temperature, dolomite δ26Mg ratio scatter in the data set decreases with increasing Mg/Ca ratio and degree of order. Specifically, δ26Mg ratio variability is reduced from ~0.7‰ at burial temperatures beneath 100°C to about ~0.2‰ at temperatures in excess of 350°C, respectively, with mean δ26Mg values ranging constantly near -1.9‰. This suggests that, at least for the rock buffered system investigated here, dolmicrite δ26Mg proxy data are conservative and preserve near pristine values even at elevated burial temperatures. At present, the main element of uncertainty is the Mg-isotope fractionation factor between (evaporated) seawater and dolomite. A possible solution to this problem includes the compilation of a data from modern sabkha environments including pore water and calcian dolomite δ26Mg isotope signatures.

Multiple episodes of dolomitization and dolomite recrystallization during shallow burial in Upper Jurassic shelf carbonates: eastern Swabian Alb, southern Germany

Science.gov (United States)

Reinhold, C.

1998-10-01

The Upper Jurassic of the eastern Swabian Alb is composed of oolitic platform sands with associated microbe-siliceous sponge mounds at the platform margins. They are surrounded by argillaceous or calcareous mudstones and marl-limestone alternations, deposited in adjacent marl basins. Partial to complete dolomitization is predominantly confined to the mound facies. Six types of dolomite, as well as one type of ankerite, document a complex diagenetic history during shallow burial with multiple episodes of dolomite formation and recrystallization. The earliest massive matrix dolomitization is Ca-rich, has slightly depleted oxygen isotope values relative to Late Jurassic seawater, and carbon isotopic values in equilibrium with Late Jurassic seawater. This initial massive matrix dolomitization occurred during latest Jurassic to earliest Cretaceous and is related to pressure dissolution during very shallow burial at temperatures of at least 50°C. Hydrologic conditions and mass-balance calculations indicate that burial compaction provided sufficient fluids for dolomitization. Mg is derived from negligibly modified seawater, that was expelled from the adjacent off-reef strata into the mound facies. Position of the mounds along the platform margins controlled the distribution of the shallow-burial dolomite. Covariant trends between textural modification, increasing stoichiometry, partial changes in trace element content (Mn, Fe, Sr) and depletion in stable isotopes as well as distinctive CL pattern illustrate two recrystallization phases of the precursor matrix dolomite during further burial at elevated temperatures. Strong Sr enrichment of the second phase of recrystallized dolomite is ascribed to Sr-rich meteoric waters descending from overlying aragonite-bearing reef limestones or evaporite-bearing peritidal carbonates. Late-stage coarsely crystalline dolomite cements occur as vug and fracture fillings and formed during burial. Ankerite, associated with sulphide and

Cyclic, Early Diagenetic Dolomite Formation in Alkaline Lake Van

Science.gov (United States)

McCormack, J.; Bontognali, T. R. R.; Immenhauser, A.; Kwiecien, O.

2017-12-01

Modern dolomite-forming environments are commonly constrained to evaporitic marine or marginal marine settings such as lagoons and sabkhas. Beside microbial mediation, high temperatures and Mg2+ concentrations in solution are factors considered important in aiding dolomite formation. Accordingly, previous studies associate the presence of dolomite within deep sediments of alkaline Lake Van (Turkey) with periods of enhanced evaporation, low lake levels and high Mg/Ca ratio. We systematically studied dolomite within the sedimentary record of Lake Van by means of XRD, SEM and stable isotope (δ18O and δ13C) mass spectrometry. First, we considered the origin of the dolomite; next, we focused on the wider implication of its presence. SEM imaging documents large dolomite crystals interwoven with clay minerals and individual crystals with different crystallographic orientations grown together, indicating space-limited growth within the sediment. According to recent climatic reconstructions for the same sequence (ICDP PALEOVAN project), the water depth of the coring site - today at 350 m - unlikely fell below 200 m. Consequently, dolomite formed below a thick water column at constantly low temperatures (supported by heavy δ18O signature). Within this environment, variations in Mg/Ca ratio, pH and alkalinity, which are constantly high, have no effect on the episodic nature of dolomite precipitation. These observations call for a re-evaluation of the palaeoenvironments often invoked to interpret intervals rich in dolomite within ancient sedimentary sequences (e.g., periods of enhanced aridity and evaporation). Further, and in contrast to previous interpretations, our dolomite concentration data backed up by ICDP PALEOVAN reconstructions suggest that intervals rich in dolomite coincide with periods of high lake level and increased humidity. High dolomite concentrations (20 - 85 % relative carbonate content) occur cyclically within the last glacial period and coincide with

Mineralogical and chemical characteristics of marble of Bela Pola deposite

International Nuclear Information System (INIS)

Shijakova-Ivanova, Tena; Boev, Blazho; Panov, Zoran; Pavlov, Dejan

2009-01-01

This paper presents mineralogical characteristics of marbles from the Bela Pola deposit. We have made mineralogical-chemical analyses of marbles and associated minerals in them. The investigation was carried out at the Faculty of natural and technical sciences - Shtip. Marbles from Bela Pola are dolomite and dolomite-calcite types. Microscope investigations have shown that marbles from Bela Pola have granoblastic structure but at some places it can be found with porphyroblastic structures. Percentage on calcite and dolomite is: 94.08% dolomite, 6.25% is calcite in white marbles. On the other hand calcite is present with 93% in gray marbles. Except dolomite and calcite also appear the following accessoring minerals: quartz, fluorite, corundum and paragonite. In general, after summarizing all the facts, which have resulted from this research we could say that, the Bela Pola marbles are massive, compact and white with high quality. In accordance to all formerly mentioned features, this marbles can be classified in the commercial group of marbles suitable for external application or internal design

Neoproterozoic marine carbonates and their paleoceanographic significance

Science.gov (United States)

Hood, Ashleigh van Smeerdijk; Wallace, Malcolm William

2018-01-01

The primary mineralogy of marine carbonate precipitates has been a crucial factor in constraining the major element composition of ancient oceans. Secular changes in Phanerozoic marine chemistry, including Mg/Ca, have been well-documented using the original carbonate mineralogy of ooids, marine cements and biominerals. However, the history of Precambrian seawater chemistry is not as well constrained, partially due to the prevalence of dolomitisation in the Precambrian geological record. The Neoproterozoic ( 1000 Ma to 541 Ma) record of primary carbonate mineralogy is documented here using a combination of literature data and new analysis of marine carbonate precipitates from the Otavi Fold Belt, Namibia, the Death Valley succession, USA and the Adelaide Fold Belt, Australia. These data suggest that the last 460 million years of the Proterozoic were dominated by aragonite and high-Mg calcite precipitation in shallow marine settings. In contrast, low-Mg calcite has only been recognised in a small number of formations. In addition to aragonite and calcite precipitation, marine dolomite precipitation was widespread in Neoproterozoic oceans, including mimetic (syn-sedimentary) dolomitisation and primary dolomite marine cementation. The combination of marine aragonite, high Mg-calcite and dolomite precipitation during the Neoproterozoic suggests extremely high seawater Mg/Ca conditions relative to Phanerozoic oceans. Marine dolomite precipitation may also be linked to widespread marine anoxia during this time.

Can Mn–S redox cycling drive sedimentary dolomite formation? A hypothesis

Energy Technology Data Exchange (ETDEWEB)

Petrash, Daniel A.; Lalonde, Stefan V.; González-Arismendi, Gabriela; Gordon, Robert A.; Méndez, José A.; Gingras, Murray K.; Konhauser, Kurt O. (CLS); (UCV-Venezuela); (CNRS-UMR); (Alberta)

2016-06-10

The formation of dolomite in modern peritidal environments is linked to the degradation of buried microbial mats, with complexation of Ca and Mg by extracellular polymeric substances (EPSs) and alkalinity generation through organic carbon respiration facilitating the nucleation of dolomite precursors. In the past two decades, microbial sulfate reduction, methanogenesis, and methanotrophy have all been considered as potential drivers of the nucleation process, but it remains unclear why dolomite formation could not also occur in suboxic sediments where abundant alkalinity is produced by processes linked to Mn(IV) and/or Fe(III) reduction coupled with the diffusion and reoxidation of reduced sulfur species. Here we report the interstitial occurrence of spheroidal aggregates of nanometer-scale Ca-rich dolomite rhombohedra within suboxic sediments associated with remnant microbial mats that developed in the peritidal zone of the Archipelago Los Roques, Venezuela. Multiple analytical tools, including EPMA, ICP-MS, synchrotron-based XRF and XRD, and spatially resolved XANES microanalyses, show that the dolomite-cemented interval exhibits depleted bulk iron concentrations, but is interstitially enriched in Mn and elemental sulfur (S⁰). Manganese occurs in several oxidation states, indicating that the dolomite-cemented interval was the locus of complex biological redox transformations characterized by coupled Mn and S cycling. The tight correspondence between sedimentary Mn and MgCO₃ concentrations further hints at a direct role for Mn during dolomitization. While additional studies are required to confirm its relevance in natural settings, we propose a model by which coupled Mn–S redox cycling may promote alkalinity generation and thus dolomite formation in manner similar to, or even more efficiently, than bacterial sulfate reduction alone.

Use of multiple attributes decision-making Technique for Order Preference by Similarity to Ideal Solution (TOPSIS for Ghare-Gheshlagh calcite in determination of optimum geochemical sampling sites

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Mansour Rezaei Azizi

2015-04-01

Full Text Available Introduction Several valuable calcite deposits are located in Ghare-Gheshlagh, south basin of Urmia Lake, NW Iran. Ghare-Gheshlagh area is situated in the northern part of tectono-sedimentary unit, forming NW part of Tertiary Sanandaj-Sirjan geological belt (Stocklin and Nabavi, 1972. The predominant rock types of the area include light color limestones (Qom Formation and Quaternary alluviums and underlined dolomite in depth (Eftekharnejhad, 1973. The thickness of these units varies between 10 cm and 6 meters and up to some hundred meters in length. In the present study, the effect of geochemical parameters responsible for precipitating calcite from the carbonate aqueous fluids is interpreted by the TOPSIS method to find the most preferable sampling sites and geochemical data. Materials and Methods A total of 20 samples were taken from a NE-SW trending profile including 15 calcites of fresh surface outcrops (5 samples per each colored calcite units in order to determine the nature of the rocks. The mineral assemblages were analyzed by optical methods in combination with XRD powder diffraction analysis. Major elements were determined by X-Ray Fluorescence Spectrometry (XRF, trace and rare earth elements were determined by Inductively Coupled Plasma Mass Spectrometry (ICP-MS in Geological Survey of Iran. Results The abundances of trace elements were normalized to the continental crust values (Taylor and McLennan, 1981. The green calcite revealed enrichment in Rb and Sr, while green and white calcite were enriched in U. The U enrichment in the green calcite indicates the reduction condition of deposition. Incompatible elements such as Ba, Th, Nb and P depleted in all calcites. Varying the Sr/Ba value between 3.18 and 5.21% indicates the continental deposition environment and non-magmatic waters as well (Cheng et al., 2013. The Sr2+ content of calcites varies from 123 to 427 ppm, indicates suitable condition for calcite precipitation. Eu anomalies

Diagenetic evolution and stable isotopes of Lower Permian platform marginal carbonates (Trogkofel Limestone, Carnic Alps, Austria)

Science.gov (United States)

Schaffhauser, Maria; Krainer, Karl; Sanders, Diethard Gerald; Spötl, Christoph

2010-05-01

The Trogkofel massif in the Carnic Alps, Austria/Italy, consists of a succession up to 400 m thick of limestones deposited along a platform margin (Trogkofel Limestone; Artinskian). The top of the Trogkofel Limestone is erosively overlain by the Tarvis Breccia. Up-section, the Trogkofel Limestone consists of well-bedded shallow-water bioclastic limestones with intercalated mud mounds, overlain by thick-bedded to unbedded limestones (bioclastic grainstones, packstones, rudstones) and cementstone mounds rich in phylloid algae, Tubiphytes, bryozoans and Archaeolithoporella. In the cementstone mounds, bioclasts are coated by thick fringes and botryoids of fibrous calcite, and of calcite spar that probably represents calcitized aragonite. Primary and intrinsic pores are filled by microbialite, and/or by mudstone to bioclastic wackestone. Shallow-water bioclastic grainstones are cemented by isopachous fringes of fibrous calcite, or by sparry calcite. Throughout the succession, evidence for meteoric-vadose dissolution is present. The Trogkofel Limestone is riddled by palaeokarstic dykes and caverns filled by (a) isopachous cement fringes up to a few decimetres thick, and/or (b) by red, geopetally-laminated lime mudstone to bio-lithoclastic wackestone; geopetal laminasets locally display convolute bedding. Small dissolution cavities are filled by grey internal sediment, or by crystal silt. Brecciated internal sediments overlain by unbrecciated, geopetally-laminated infillings record deformation during or after deposition of the Trogkofel Limestone. Polyphase fractures cemented by calcite may cross-cut both internal sediments and host rock. In the Trogkofel Limestone, local dolomitization is common. Replacement dolomites show a wide range of shapes and fabrics, including: (a) fine-crystalline anhedral xenotopic fabric, (b) coarse-crystalline subhedral to euhedral, hypidiotopic to idiotopic fabric of turbid or optically zoned crystals, and (c) saddle dolomite as replacement

Intracrystalline deformation of calcite

NARCIS (Netherlands)

Bresser, J.H.P. de

1991-01-01

It is well established from observations on natural calcite tectonites that intracrystalline plastic mechanisms are important during the deformation of calcite rocks in nature. In this thesis, new data are presented on fundamental aspects of deformation behaviour of calcite under conditions where

Calcite growth-rate inhibition by fulvic acid and magnesium ion—Possible influence on biogenic calcite formation

Science.gov (United States)

Reddy, Michael M.

2012-01-01

Increases in ocean surface water dissolved carbon dioxide (CO2) concentrations retard biocalcification by reducing calcite supersaturation (Ωc). Reduced calcification rates may influence growth-rate dependent magnesium ion (Mg) incorporation into biogenic calcite modifying the use of calcifying organisms as paleoclimate proxies. Fulvic acid (FA) at biocalcification sites may further reduce calcification rates. Calcite growth-rate inhibition by FA and Mg, two common constituents of seawater and soil water involved in the formation of biogenic calcite, was measured separately and in combination under identical, highly reproducible experimental conditions. Calcite growth rates (pH=8.5 and Ωc=4.5) are reduced by FA (0.5 mg/L) to 47% and by Mg (10−4 M) to 38%, compared to control experiments containing no added growth-rate inhibitor. Humic acid (HA) is twice as effective a calcite growth-rate inhibitor as FA. Calcite growth rate in the presence of both FA (0.5 mg/L) and Mg (10−4 M) is reduced to 5% of the control rate. Mg inhibits calcite growth rates by substitution for calcium ion at the growth site. In contrast, FA inhibits calcite growth rates by binding multiple carboxylate groups on the calcite surface. FA and Mg together have an increased affinity for the calcite growth sites reducing calcite growth rates.

Nanometer-scale features in dolomite from Pennsylvanian rocks, Paradox Basin, Utah

Science.gov (United States)

Gournay, Jonas P.; Kirkland, Brenda L.; Folk, Robert L.; Lynch, F. Leo

1999-07-01

Scanning electron microscopy reveals an association between early dolomite in the Pennsylvanian Desert Creek (Paradox Fm.) and small (approximately 0.1 μm) nanometer-scale textures, termed `nannobacteria'. Three diagenetically distinct dolomites are present: early dolomite, limpid dolomite, and baroque dolomite. In this study, only the early dolomite contained nanometer-scale features. These textures occur as discrete balls and rods, clumps of balls, and chains of balls. Precipitation experiments demonstrate that these textures may be the result of precipitation in an organic-rich micro-environment. The presence of these nanometer-scale textures in Pennsylvanian rocks suggests that these early dolomites precipitated in organic-rich, bacterial environments.

Textural and isotopic evidence for Ca-Mg carbonate pedogenesis

Science.gov (United States)

Diaz-Hernandez, J. L.; Sánchez-Navas, A.; Delgado, A.; Yepes, J.; Garcia-Casco, A.

2018-02-01

Models for evaluating the terrestrial carbon cycle must take into account not only soil organic carbon, represented by a mixture of plant and animal remains, but also soil inorganic carbon, contained in minerals, mainly in calcite and dolomite. Thick soil caliches derived from weathering of mafic and ultramafic rocks must be considered as sinks for carbon storage in soils. The formation of calcite and dolomite from pedogenic alteration of volcanic tephras under an aridic moisture regime is studied in an unusually thick 3-m soil profile on Gran Canaria island (Canary Islands, Spain). The biological activity of the pedogenic environment (soil respiration) releases CO2 incorporated as dissolved inorganic carbon (DIC) in waters. It drives the formation of low-magnesian calcite and calcian dolomite over basaltic substrates, with a δ13C negative signature (-8 to -6‰ vs. V-PDB). Precipitation of authigenic carbonates in the soil is accompanied by the formation of Mg-rich clay minerals and quartz after the weathering of basalts. Mineralogical, textural, compositional, and isotopic variations throughout the soil profile studied indicate that dolomite formed at greater depths and earlier than the calcite. The isotopic signatures of the surficial calcite and deeper dolomite crusts are primary and resulted from the dissolution-precipitation cycles that led to the formation of both types of caliches under different physicochemical conditions. Dolomite formed within a clay-rich matrix through diffusive transport of reactants. It is precipitated from water with more negative δ18O values (-1.5 to -3.5‰ vs. V-SMOW) in the subsoil compared to those of water in equilibrium with surficial calcite. Thus, calcite precipitated after dolomite, and directly from percolating solutions in equilibrium with vadose water enriched in δ18O (-0.5 to +1.5‰) due to the evaporation processes. The accumulation of inorganic carbon reaches 586.1 kg m-2 in the soil studied, which means that the

Ferroan Dolomitization by Seawater Interaction with Mafic Igneous Dikes and Carbonate Host Rock at the Latemar Platform, Dolomites, Italy: Numerical Modeling of Spatial, Temporal, and Temperature Data

Directory of Open Access Journals (Sweden)

K. Blomme

2017-01-01

Full Text Available Numerous publications address the petrogenesis of the partially dolomitized Latemar carbonate platform, Italy. A common factor is interpretation of geochemical data in terms of heating via regional igneous activity that provided kinetically favorable conditions for replacement dolomitization. New field, petrographic, XRD, and geochemical data demonstrate a spatial, temporal, and geochemical link between replacement dolomite and local mafic igneous dikes that pervasively intrude the platform. Dikes are dominated by strongly altered plagioclase and clinopyroxene. Significantly, where ferroan dolomite is present, it borders dikes. We hypothesize that seawater interacted with mafic minerals, causing Fe enrichment in the fluid that subsequently participated in dolomitization. This hypothesis was tested numerically through thermodynamic (MELTS, Arxim-GEM and reactive flow (Arxim-LMA simulations. Results confirm that seawater becomes Fe-enriched during interaction with clinopyroxene (diopside-hedenbergite and plagioclase (anorthite-albite-orthoclase solid solutions. Reaction of modified seawater with limestone causes ferroan and nonferroan replacement dolomitization. Dolomite quantities are strongly influenced by temperature. At 40 to 80°C, ferroan dolomite proportions decrease with increasing temperature, indicating that Latemar dolomitization likely occurred at lower temperatures. This relationship between igneous dikes and dolomitization may have general significance due to the widespread association of carbonates with rifting-related igneous environments.

Evolution and the Calcite Eye Lens

OpenAIRE

Williams, Vernon L.

2013-01-01

Calcite is a uniaxial, birefringent crystal, which in its optically transparent form, has been used for animal eye lenses, the trilobite being one such animal. Because of the calcite birefringence there is a difficulty in using calcite as a lens. When the propagation direction of incoming light is not exactly on the c-axis, the mages blur. In this paper, calcite blurring is evaluated, and the non-blurring by a crystallin eye lens is compared to a calcite one.

Nickel adsorption on chalk and calcite

DEFF Research Database (Denmark)

Belova, Dina Alexandrovna; Lakshtanov, Leonid; Carneiro, J.F.

2014-01-01

Nickel uptake from solution by two types of chalk and calcite was investigated in batch sorption studies. The goal was to understand the difference in sorption behavior between synthetic and biogenic calcite. Experiments at atmospheric partial pressure of CO2, in solutions equilibrated with calcite...... = - 1.12 on calcite and log KNi = - 0.43 and - 0.50 on the two chalk samples. The study confirms that synthetic calcite and chalk both take up nickel, but Ni binds more strongly on the biogenic calcite than on inorganically precipitated, synthetic powder, because of the presence of trace amounts...... of polysaccharides and clay nanoparticles on the chalk surface....

Identification of Oxide Compound in Dolomite Mineral from Aceh Tamiang Region

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Nirmala Sari

2013-08-01

Full Text Available Indonesia has abundant mineral especially carbonate-based mineral, ike dolomite. Particularly in Aceh province's, the largest dolomite deposits is available in Aceh Tamiang district around 1.9 billion tons. Unfortunately, current use of dolomite in the industry and other applications is still limited. In this work we report the advanced preparation of dolomite using calcinations method. Whereas, with this method, the dolomite mineral can be processed into calcium and magnesium oxide which has a very wide field of application and higher values. To obtain optimal results, we also identify the effect of temperature on the formation of oxide compounds. Preliminary study using XRF founded that dolomite in village Selamat is known as the highest concentration of CaO (61.20% followed by MgO (25.28%. It is also showed that the main phase obtained by XRD is dolomite (CaMg(CO32. Furthermore, after the calcinations process at 700 °C, it was founded that the formation of dolomite were CaCO3 and MgO, whereas at temperatures of 900 °C mostly the CaCO3 has decomposed into CaO. SEM observations showed that dolomite has the composition of particles distributed homogeneously along the particle agglomerate when it calcinations.

Aerobic microbial dolomite at the nanometer scale : Implications for the geologic record

NARCIS (Netherlands)

Sánchez-Román, Mónica; Vasconcelos, Crisógono; Schmid, Thomas; Dittrich, Maria; McKenzie, Judith A.; Zenobi, Renato; Rivadeneyra, Maria A.

2008-01-01

Microbial experiments are the only proven approach to produce experimental dolomite under Earth's surface conditions. Although microbial metabolisms are known to induce dolomite precipitation by favoring dolomite growth kinetics, the involvement of microbes in the dolomite nucleation process is

Controls on Cyclic Formation of Quaternary Early Diagenetic Dolomite

Science.gov (United States)

McCormack, J.; Bontognali, T. R. R.; Immenhauser, A.; Kwiecien, O.

2018-04-01

The origin of sedimentary dolomite and the factors that control its formation within the geological record remain speculative. In most models, dolomite formation is linked to evaporative conditions, high water temperature, increasing Mg/Ca ratio, increasing alkalinity, and high amounts of biomass. Here we challenge these archetypal views, by documenting a case example of Quaternary dolomite which formed in Lake Van at constantly low temperature (stress, resulting from reventilation of the water-sediment interface. Independently from the validity of this hypothesis, our results call for a reevaluation of the paleoenvironmental conditions often invoked for early diagenetic dolomite-rich intervals within sedimentary sequences and for caution when interpreting time series of subrecent lacustrine carbonates.

High salinity facilitates dolomite precipitation mediated by Haloferax volcanii DS52

Science.gov (United States)

Qiu, Xuan; Wang, Hongmei; Yao, Yanchen; Duan, Yong

2017-08-01

Although most modern dolomites occur in hypersaline environments, the effects of elevated salinity on the microbial mediation of dolomite precipitation have not been fully evaluated. Here we report results of dolomite precipitation in association with a batch culture of Haloferax volcanii DS52, a halophilic archaeon, under various salinities (from 120‰ to 360‰) and the impact of salinity on microbe-mediated dolomite formation. The mineral phases, morphology and atomic arrangement of the precipitates were analyzed by XRD, SEM and TEM, respectively. The amount of amino acids on the archaeal cell surface was quantified by HPLC/MS. The XRD analysis indicated that disordered dolomite formed successfully with the facilitation of cells harvested from cultures with relatively high salinities (200‰ and 280‰) but was not observed in association with cells harvested from cultures with lower salinity (120‰) or the lysates of cells harvested from extremely high salinity (360‰). The TEM analysis demonstrated that the crystals from cultures with a salinity of 200‰ closely matched that of dolomite. Importantly, we found that more carboxyl groups were presented on the cell surface under high salinity conditions to resist the high osmotic pressure, which may result in the subsequent promotion of dolomite formation. Our finding suggests a link between variations in the hydro-chemical conditions and the formation of dolomite via microbial metabolic activity and enhances our understanding about the mechanism of microbially mediated dolomite formation under high salinity conditions.

Arsenic uptake in bacterial calcite

Science.gov (United States)

Catelani, Tiziano; Perito, Brunella; Bellucci, Francesco; Lee, Sang Soo; Fenter, Paul; Newville, Matthew; Rimondi, Valentina; Pratesi, Giovanni; Costagliola, Pilario

2018-02-01

Bio-mediated processes for arsenic (As) uptake in calcite were investigated by means of X-ray Diffraction (XRD) and X-ray Absorption Spectroscopy (XAS) coupled with X-ray Fluorescence measurements. The environmental bacterial strain Bacillus licheniformis BD5, sampled at the Bullicame Hot Springs (Viterbo, Central Italy), was used to synthesize calcite from As-enriched growth media. Both liquid and solid cultures were applied to simulate planktonic and biofilm community environments, respectively. Bacterial calcite samples cultured in liquid media had an As enrichment factor (Kd) 50 times higher than that from solid media. The XRD analysis revealed an elongation of the crystal lattice along the c axis (by 0.03 Å) for biogenic calcite, which likely resulted from the substitution of larger arsenate for carbonate in the crystal. The XAS data also showed a clear difference in the oxidation state of sorbed As between bacterial and abiotic calcite. Abiotic chemical processes yielded predominantly As(V) uptake whereas bacterial precipitation processes led to the uptake of both As(III) and As(V). The presence of As(III) in bacterial calcite is proposed to result from subsequent reduction of arsenate to arsenite by bacterial activities. To the best of our knowledge, this is the first experimental observation of the incorporation of As(III) in the calcite crystal lattice, revealing a critical role of biochemical processes for the As cycling in nature.

Arsenic uptake in bacterial calcite

Energy Technology Data Exchange (ETDEWEB)

Catelani, Tiziano; Perito, Brunella; Bellucci, Francesco; Lee, Sang Soo; Fenter, Paul; Newville, Matthew G.; Rimondi, Valentina; Pratesi, Giovanni; Costagliola, Pilario

2018-02-01

Bio-mediated processes for arsenic (As) uptake in calcite were investigated by means of X-ray Diffraction (XRD) and Xray Absorption Spectroscopy (XAS) coupled with X-ray Fluorescence measurements. The environmental bacterial strain Bacillus licheniformis BD5, sampled at the Bullicame Hot Springs (Viterbo, Central Italy), was used to synthesize calcite from As-enriched growth media. Both liquid and solid cultures were applied to simulate planktonic and biofilm community environments, respectively. Bacterial calcite samples cultured in liquid media had an As enrichment factor (Kd) 50 times higher than that from solid media. The XRD analysis revealed an elongation of the crystal lattice along the c axis (by 0.03Å) for biogenic calcite, which likely resulted from the substitution of larger arsenate for carbonate in the crystal. The XAS data also showed a clear difference in the oxidation state of sorbed As between bacterial and abiotic calcite. Abiotic chemical processes yielded predominantly As(V) uptake whereas bacterial precipitation processes led to the uptake of both As(III) and As(V). The presence of As(III) in bacterial calcite is proposed to result from subsequent reduction of arsenate to arsenite by bacterial activities. To the best of our knowledge, this is the first experimental observation of the incorporation of As(III) in the calcite crystal lattice, revealing a critical role of biochemical processes for the As cycling in nature.

Diagenetic modification of Knox evaporative-dolomite geochemistry by middle Ordovician paleoaquifer/burial fluids

Energy Technology Data Exchange (ETDEWEB)

Montanez, I.P.; Read, J.F.

1986-05-01

Early Ordovician upper Knox cyclic carbonates (100,000-year periods) were deposited on a ramp in a semiarid setting. Inner ramp facies are completely dolomitized, whereas only cycle caps on the outer ramp are dolomite. Laminite caps on leading edges of prograding flats were dolomitized by evaporative, storm-recharged marine waters that precipitated CoCO/sub 3/ and minor amounts of CaSO/sub 4/. Subtidal facies beneath interiors of supratidal flats (up to 200 km wide)were dolomitized by shallow subsurface brines as the flats prograded. Inner ramp areas existed as supretidal flats for as long as 100,000 years, hence only there are sequences completely dolomitized. Tidal-flat dolomites consist of euhedral to subhedral fabric preservation mosaics (crystals 5-50 ..mu..m, and up to 300 ..mu..m in replaced pelletal layers). Dolomitized subtidal sediments are composed of 20-200 ..mu..m dolomite crystals. Most of the early dolomites are fabric retentive initially, becoming more fabric destructive with increasing exposure to dolomitizing fluids. Fe values are up to 2000 ppm, and Mn values are up to 500 ppm. delta/sup 18/O values show strong geographic control, with samples depleted (up to - 7 per thousand) relative to pristine evaporative dolomites derived from concentrated Ordovician seawater. Burial dolomites are enriched in Fe (up to 14,000 ppm) and depleted in delta/sup 18/O, suggesting precipitation from basinal brines at elevated temperatures. Geochemical data suggest that evaporative dolomites have undergone modification by isotopically lighter fluids. Alteration most likely occurred within a Middle Ordovician meteoric aquifer system or less likely by later Paleozoic basinal brines. Regional geologic data for Knox Group carbonates throughout the eastern US are vital in constraining dolomitization models.

Messinian Salinity Crisis' Primary Evaporites: the shallow gypsum vs. deep dolomite formation paradox solved

Science.gov (United States)

De Lange, G. J.; Krijgsman, W.

2015-12-01

The Messinian Salinity Crisis (MSC) is a dramatic event that took place ~ 5.9 Ma ago, resulting in deposition of 1-3 km thick evaporites at the Mediterranean seafloor. A considerable, long-lasting controversy existed on the modes of their formation, including the observed shallow gypsum versus deep dolostone deposits for the early phase of MSC. The onset of MSC is marked by deposition of gypsum/sapropel-like alternations, thought to relate to arid/humid climate conditions at a precessional rhythm. Gypsum precipitation only occurred at marginal- and dolomite formation at deeper settings. A range of potential explanations was given, most of which cannot satisfactorily explain all observations. Biogeochemical processes during MSC are commonly neglected but may explain that different deposits formed in shallow vs deep environments without exceptional physical boundary conditions for each. A unifying mechanism is presented in which gypsum formation occurs at all shallow water depths but its preservation is limited to shallow sedimentary settings. In contrast, ongoing deep-basin anoxic organic matter (OM) degradation processes result in dolomite formation. Gypsum precipitation in evaporating seawater takes place at 3-7 times concentrated seawater; seawater is always oversaturated relative to dolomite but its formation is inhibited by the presence of dissolved sulphate. Thus conditions for formation of gypsum exclude those for formation of dolomite and vice versa. Another process linking the saturation states of gypsum and dolomite is that of OM degradation by sulphate reduction. In stagnant deep water, ongoing OM-degradation may result in reducing the sulphate and enhancing the dissolved carbonate content. Such low-sulphate / high carbonate conditions in MSC deepwater are. unfavorable for gypsum preservation and favorable for dolomite formation, and always coincide with anoxic, i.e. oxygen-free conditions. Including dynamic biogeochemical processes in the thusfar static

Metal Sorption to Dolomite Surfaces

International Nuclear Information System (INIS)

Brady, P.V.; Papenguth, H.W.; Kelly, J.W.

1999-01-01

Potential human intrusion into the Waste Isolation Pilot Plant (WIPP) might release actinides into the Culebra Dolomite where sorption reactions will affect of radiotoxicity from the repository. Using a limited residence time reactor the authors have measured Ca, Mg, Nd adsorption/exchange as a function of ionic strength, P CO2 , and pH at 25 C. By the same approach, but using as input radioactive tracers, adsorption/exchange of Am, Pu, U, and Np on dolomite were measured as a function of ionic strength, P CO2 , and pH at 25 C. Metal adsorption is typically favored at high pH. Calcium and Mg adsorb in near-stoichiometric proportions except at high pH. Adsorption of Ca and Mg is diminished at high ionic strengths (e.g., 0.5M NaCl) pointing to association of Na + with the dolomite surface, and the possibility that Ca and Mg sorb as hydrated, outer-sphere complexes. Sulfate amplifies sorption of Ca and Mg, and possibly Nd as well. Exchange of Nd for surface Ca is favored at high pH, and when Ca levels are low. Exchange for Ca appears to control attachment of actinides to dolomite as well, and high levels of Ca 2+ in solution will decrease Kds. At the same time, to the extent that high P CO2 increase Ca 2+ levels, JK d s will decrease with CO 2 levels as well, but only if sorbing actinide-carbonate complexes are not observed to form (Am-carbonate complexes appear to sorb; Pu-complexes might sorb as well; U-carbonate complexation leads to desorption). This indirect CO 2 effect is observed primarily at, and above, neutral pH. High NaCl levels do not appear to affect to actinide K d s

Coprecipitation of cadmium with calcite

International Nuclear Information System (INIS)

Fujino, Osamu; Kumagai, Tetsu; Shigematsu, Tsunenobu; Matsui, Masakazu

1976-01-01

The distribution of cadmium between precipitates of calcite and saturated aqueous solution was measured at 25 0 C to understand the distribution of cadmium in the bivalves. Calcite was precipitated from calcium bicarbonate solution by the gradual release of carbon dioxide. The cadmium ions were coprecipitated in calcite, obeying the logarithmic distribution law. The apparent distribution coefficient was decreased as α, α'-dipyridyl increased, but the true distribution coefficient was found to be an almost constant value, 560. This value is fairly close to the ratio of solubility product constants K sub(calcite)/K sub(CdCO 3 ), 890. This suggests that the deviation of the present solid solution from ideality is not very large. (auth.)

Sealing process with calcite in the Nojima active fault zone revealed from isotope analysis of calcite

International Nuclear Information System (INIS)

Arai, Takashi; Tsukahara, Hiroaki; Morikiyo, Toshiro

2003-01-01

The Nojima fault appeared on the surface in the northern part of Awaji Island, central Japan as a result of the Hyogo-ken Nanbu earthquake (1995, M=7.2). Active fault drilling was performed by the Disaster Prevention Research Institute (DPRI), Kyoto University, and core samples were retrieved from 1410 to 1710 m, which were composed of intact and fractured granodiorites. We obtained calcite samples and gas samples from the vein in marginal fracture and non-fracture zones. We analyzed the carbon and oxygen isotope ratios of calcite and carbon dioxide to investigate the characteristic isotope ratios of fluids in the active fault zone, to estimate the origins of fluids, and to determine the sealing process of fractures. The analyzed values of carbon and oxygen isotope ratios of calcite were -10.3 to -7.2 per mille, 18 to 23 per mille, respectively, and carbon isotope ratios of CO 2 were -21 to -17 per mille. If carbon isotope ratios of calcite were at equilibrium with those of CO 2 , the precipitation temperature of calcite is calculated to be 30 to 50 deg C. This temperature is consistent with the present temperature of the depth where drilling cores were retrieved. Oxygen isotope ratios of H 2 O that, precipitated calcite were calculated to be -1.8 to -5.5 per mille. These values indicate calcite were precipitated from mixed fluids of sea water and meteoric water. Therefore, the marginal fracture zone of the Nojima fault was sealed with calcite, which was generated from mixing of sea water and meteoric water in situ. (author)

Nanotoxicity of dolomite mineral of commercial importance in India.

Science.gov (United States)

Patil, Govil; Khan, Mohd Imran; Akhtar, Mohd Javed; Ashquin, Mohd; Sultana, Sarwat; Ahmad, Iqbal

2011-02-01

The risk of occupational exposure to dolomite, an important mineral exists both in organized as well as unorganized sectors. Toxicological profiles of bulk dolomite are meagerly known in general and its nanotoxicity in particular. Effects of micro- and nano particles on cell viability, LDH leakage and markers of oxidative stress were observed. The study indicated that cytotoxicity of dolomite nanoparticles is significantly higher than the microparticles. The study thus suggests for the prescription of exposure limit for nanodolomite in the best interest of health of workers at risk of exposure under mining, milling and industrial environment.

Origins and Geochemistry of Oolitic Dolomite of the Feixianguan Formation from the Yudongzi Outcrop, Northwest Sichuan Basin, China

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Liya Zhang

2017-07-01

Full Text Available The topic of dolomite formation has long presented a challenge to researchers. In this study, the origin of widely occurring oolitic dolomites from the Yudongzi outcrop in the lower Triassic Feixianguan formation in northwest Sichuan, China, was investigated through petrographic observations, and mineralogical and geochemical analysis. Analytical methods used include cathodoluminescence, X-ray diffraction, stable isotopes, and electronic microprobe characterization. The dolomites were categorized into three major genetic types according to their textural and structural characteristics, which reflect their various origins. The first genetic type of these dolomites, seepage reflux dolomitization, occurs in marly to microcrystalline dolomite during the penecontemporaneous stage, and displays negatively skewed δ18Ο (−2.83‰ Pee Dee Belemnite (PDB, positively skewed δ13C (2.71‰ PDB, a low degree of order (0.48, and 87Sr/86Sr ratios of 0.707509–0.707634, indicating involvement of a Mg-rich brine fluid in an open evaporative environment. The second type, shallow burial dolomitization, is the most significant genetic type of dolomite reservoir in this area. This process produced dominantly silty to fine crystalline dolomite in a platform-margin oolitic beach facies with negatively skewed δ18Ο (−3.26‰ PDB, positively skewed δ13C (1.88‰ PDB, a high degree of order (0.70, and 87Sr/86Sr ratios of 0.707318–0.707661, which are related to seawater-derived fluids in a shallow burial environment. The third type is moderate to deep burial dolomitization, and is the main process responsible for zoned dolomite and dolomite with cloudy cores and clear rims (CCCR dolomite, which have the most strongly negatively skewed δ18Ο (−7.32‰ PDB, positively skewed δ13C (3.02‰ PDB, and 87Sr/86Sr ratios of 0.707217–0.707855, representing diagenetic alteration and fluid flow in a closed environment. These findings indicate that dolomite was likely

Origin of calcite in the glacigenic Virttaankangas complex

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Nina M. Kortelainen

2007-01-01

Full Text Available Groundwaters of the glacigenic Virttaankangas complex in southern Finland are characterized by high pH values ranging up to 9.5. These values are significantly higher than those observed in silicate-rich shallow groundwater formations in crystalline bedrock areas. TheVirttaankangas sediments were discovered to contain small amounts of fine grained, dispersed calcite, which has a high tendency to increase the pH of local groundwaters. The primary goal of this study was to determine the mode of occurrence of calcite and to identifyits sources. The mineralogy of the glacigenic Virttaankangas complex was studied using material from 21 sediment drill cores. Fine-grained calcite is present in trace amounts (<< 1.4 % in the glaciofluvial and glaciolacustrine depositional units of the Virttaankangas complex. The topmost littoral sands were practically devoid of calcite. The isotope records of carbon and oxygen, the angular morphology of the grains and the uniform dispersion of calcite in the complex suggest a clastic origin for calcite, with no evidence for in-situ precipitation. In order to constrain the source of calcite, the isotopic composition of carbon and oxygen in five calcite samples was compared to the isotopic data from five carbonate rock erratics and eight crystalline bedrock samples from the region. Based on carbon and oxygen isotope ratios and chemical compositions, the dispersed calcite grains of the Virttaankangas complex appear to have been derived from the Mesoproterozoic Satakunta Formation, some 30 km NW from the Virttaankangas area. In sandstone, calcite is predominantly present as diagenetic cement in grain interspaces, concretions and interlayers. The source of detrital calcite was unexpected, as prior to this study the Satakunta sandstone hasnot been known to contain calcite.

Microbial dolomite crusts from the carbonate platform off western India

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P.; Kessarkar, P.M.; Krumbein, W.E.; Krajewski, K.P.; Schneider, R.J.

Association of Sedimentologists, Sedimentology, 50, 819-830 Microbial dolomite crusts off western India 821 dolomite crusts [2 x 2·5 em to 3 x 0'5 em) and pebbles occur within these sediments. METHODS Thin sections of the crusts were studied petro graphically....E. (19S7) Holocene dolomitization Df supr

Production of biodiesel from palm oil using modified Malaysian natural dolomites

International Nuclear Information System (INIS)

Shajaratun Nur, Z.A.; Taufiq-Yap, Y.H.; Rabiah Nizah, M.F.; Teo, Siow Hwa; Syazwani, O.N.; Islam, Aminul

2014-01-01

Highlights: • Transesterification was carried out using modified Malaysian natural dolomite catalyst. • Characterizations of the catalyst were performed by using XRD, TPD-CO 2 , BET and SEM. • Maximum biodiesel conversion of 100% was achieved from SnO 2 /dolomite catalyst. • The yield was affected by the surface are as well as the basicity of catalyst. • The transesterification reaction gave significant conversion with relatively lower amount of catalyst. - Abstract: Calcined dolomite (AD), produced by calcination of Malaysian dolomite (UD) promotes a potential natural catalyst for biodiesel production from palm oil with the conversion of 99.98%. The catalysts were characterized by using X-ray Diffractometer (XRD), Brunauer–Emmet–Teller (BET) surface area, Scanning Electron Microscopy (SEM) and Temperature Programmed Desorption (TPD) of CO 2 . All catalysts were then employed for transesterification reaction under different conditions (time, methanol to oil molar ratio and amount of catalyst). SnO 2 doped on activated dolomite (SD) shows an optimum conversion (99.98%) at conditions, i.e. 15:1 methanol to oil molar ratio in 4 h compared to ZnO doped on activated dolomite (ZD) and AD. The catalytic activities of these catalysts were found to be depending on the basicity as well as the surface area of the catalyst used

Carbonate Minerals with Magnesium in Triassic Terebratula Limestone in the Term of Limestone with Magnesium Application as a Sorbent in Desulfurization of Flue Gases

Science.gov (United States)

Stanienda-Pilecki, Katarzyna

2017-09-01

This article presents the results of studies of Triassic (Muschelkalk) carbonate rock samples of the Terebratula Beds taken from the area of the Polish part of the Germanic Basin. It is the area of Opole Silesia. The rocks were studied in the term of possibility of limestone with magnesium application in desulfurization of flue gases executed in power plants. Characteristic features of especially carbonate phases including magnesium-low-Mg calcite, high-Mg calcite, dolomite and huntite were presented in the article. They were studied to show that the presence of carbonate phases with magnesium, especially high-Mg calcite makes the desulfurization process more effective. Selected rock samples were examined using a microscope with polarized, transmitted light, X-ray diffraction, microprobe measurements and FTIR spectroscopy. The results of studies show a domination of low magnesium calcite in the limestones of the Terebratula Beds. In some samples dolomite and lower amounts of high-Mg calcite occurred. Moreover, huntite was identified. The studies were very important, because carbonate phases like high-Mg calcite and huntite which occurred in rocks of the Triassic Terebratula Beds were not investigated in details by other scientists but they presence in limestone sorbent could influence the effectiveness of desulfurization process.

Structure and Stability of High-Pressure Dolomite with Implications for the Earth's Deep Carbon Cycle

Science.gov (United States)

Solomatova, N. V.; Asimow, P. D.

2014-12-01

Carbon is subducted into the mantle primarily in the form of metasomatically calcium-enriched basaltic rock, calcified serpentinites and carbonaceous ooze. The fate of these carbonates in subduction zones is not well understood. End-member CaMg(CO3)2 dolomite typically breaks down into two carbonates at 2-7 GPa, which may further decompose to oxides and CO2-bearing fluid. However, high-pressure X-ray diffraction experiments have recently shown that the presence of iron may be sufficient to stabilize dolomite I to high pressures, allowing the transformation to dolomite II at 17 GPa and subsequently to dolomite III at 35 GPa [1][2]. Such phases may be a principal host for deeply subducted carbon. The structure and equation of state of these high-pressure phases is debated and the effect of varying concentrations of iron is unknown, creating a need for theoretical calculations. Here we compare calculated dolomite structures to experimentally observed phases. Using the Vienna ab-initio simulation package (VASP) interfaced with a genetic algorithm that predicts crystal structures (USPEX), a monoclinic phase with space group 5 ("dolomite sg5") was found for pure end-member dolomite. Dolomite sg5 has a lower energy than reported dolomite structures and an equation of state that resembles that of dolomite III. It is possible that dolomite sg5 is not achieved experimentally due to a large energy barrier and a correspondingly large required volume drop, resulting in the transformation to metastable dolomite II. Due to the complex energy landscape for candidate high-pressure dolomite structures, it is likely that several competing polymorphs exist. Determining the behavior of high-pressure Ca-Mg-Fe(-Mn) dolomite phases in subduction environments is critical for our understanding of the Earth's deep carbon cycle and supercell calculations with Fe substitution are in progress. [1] Mao, Z., Armentrout, M., Rainey, E., Manning, C. E., Dera, P., Prakapenka, V. B., and Kavner, A

Interaction mechanisms of europium and nickel with calcite

International Nuclear Information System (INIS)

Sabau, Andrea

2015-01-01

In the context of the safety assessment of an underground repository for nuclear waste, sorption reactions are one of the main processes to take into account to predict the migration of the radionuclides which might be transferred from the waste canisters to underground waters over geological time scales. Sorption of aqueous species on minerals can include adsorption processes, surface (co)-precipitation, and even incorporation in the bulk of the material, which can lead to the irreversibility of some sorption reactions. This work is focused on two elements: Eu(III) as an analogue of trivalent actinides and Ni(II) as activation product. Calcite was chosen as adsorbent due to its presence in Callovian-Oxfordian clay rocks. Our study combines batch experiments with spectroscopic techniques (TRLFS, RBS and SEM-EDXS) to elucidate the mechanisms occurring at Eu(III)/Ni(II) calcite interface. To obtain a better understanding on the systems, before starting sorption experiments, aqueous chemistry of Eu(III) and Ni(II) was carefully investigated. Macroscopic results showed a strong retention of Eu(III) on calcite, no matter the initial concentration, contact time and CO 2 partial pressure. Ni(II) was also readily sorbed by calcite, but the retention was influenced by contact time and concentration. Time-dependent sorption experiments showed a marked and slow increase of retention upon a long time range (up to 4 months).Desorption results indicated a partly reversible sorption for Ni(II). TRLFS highlighted the influence of initial concentration and contact time on the interaction of Eu(III) with calcite. With the help of RBS and SEM-EDXS, it enabled to discriminate between different mechanisms like surface precipitation, inner-sphere complexation and incorporation. RBS showed incorporation of Eu(III) into calcite up to 250 nm, contrary to Ni(II) which was located at the surface. (author) [fr

Geochemical and isotope aspects of calcite deposits and calcitic marbles hosts mineralizations, Serra do Carumbe, Vale do Ribeira, Parana state, Brazil

International Nuclear Information System (INIS)

Venusso, Gerson Caetano; Andrade e Silva, Antonio C. Gondim de

2011-01-01

The calcite deposits and the calcitic marbles hosts occur in Serra do Carumbe, in the Vale do Ribeira region, Parana State, were studied in their geochemical and isotopic aspects viewing the gathering of information about their genesis and economical use. The calcite deposits are constituted by veins and lenses, being three of them concordant and one discordant in relation to the S_0 from the hosting marbles. In these deposits four main types of calcite were recognized: rombohedrical, fibrous, banded and microcrystalline. The calcite reveal themselves having high purity, with CaO concentration above 55.30% and MgO below 0.42%. The lithogeochemical study of the marbles sequence was conducted in various suites revealing an uniformity in their composition, with high values of CaO (above 46.92%) in relation to the MgO values (below 3,37%), what favors their use for cement manufacture, except in sectors that suffered fault influences, where the marbles are impure (siliceous, magnesian, ferruginous and aluminous). Regarding their trace elements content, the hosting calcitic marbles have higher concentrations than the calcite, in the elements Sr, B, Ba and Mg, what makes evident their different formation environments. The δ"1"3C values from calcite range from –9,02 to –12,24 ‰ , referring to PDB, while the values δ"1"8O range from 24,48 to 25,23 ‰, referring to SMOW; meanwhile, for the calcitic marbles, the δ"1"3C values range from –4,03 to 1,42‰ and of δ"1"8O range from 20,71 to 23,00 ‰. The high δ"1"8O values would indicate enrichment referring to the interaction of the calcite's generator fluid with the carbonatic host rock. The δ"1"3C values indicate origin from hydrothermal solution for the calcite, although they would not allow to conclude if their sources would be superficial or profound. As for the hosting calcitic marbles, the isotopic values indicate genesis from pre-cambrian marine limestone. (author)

Mechanisms of metasomatism in the calcite-pitchblende system: 2. Replacement of pitchblende by calcite

International Nuclear Information System (INIS)

Dymkov, Yu.M.

1996-01-01

The principal mechanisms of the nasturan replacement by calcite -intrametasomatism, frontal metasomatism, dispersive metasomatism, and transformative metasomatism - are discussed in terms of G.L. Pospelov's (1973) concept. The main chemical condition required by the process is an oxidized environment, in which the tetravalent uranium of pitchblende or transitional reduced phases (coffinite) oxidizes to yield readily soluble uranyl compounds. The latter are replaced by calcite

Preparation and Characterization of Malaysian Dolomites as a Tar Cracking Catalyst in Biomass Gasification Process

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M. A. A. Mohammed

2013-01-01

Full Text Available Three types of local Malaysian dolomites were characterized to investigate their suitability for use as tar-cracking catalysts in the biomass gasification process. The dolomites were calcined to examine the effect of the calcination process on dolomite’s catalytic activity and properties. The modifications undergone by dolomites consequent to thermal treatment were investigated using various analytical methods. Thermogravimetric and differential thermal analyses indicated that the dolomites underwent two stages of decomposition during the calcination process. The X-ray diffraction and Fourier-transform infrared spectra analyses showed that thermal treatment of dolomite played a significant role in the disappearance of the CaMg(CO32 phase, producing the MgO-CaO form of dolomite. The scanning electron microscopy microphotographs of dolomite indicated that the morphological properties were profoundly affected by the calcination process, which led to the formation of a highly porous surface with small spherical particles. In addition, the calcination of dolomite led to the elimination of carbon dioxide and increases in the values of the specific surface area and average pore diameter, as indicated by surface area analysis. The results showed that calcined Malaysian dolomites have great potential to be applied as tar-cracking catalysts in the biomass gasification process based on their favorable physical properties.

High-Magnesian Calcite Mesocrystals : A Coordination Chemistry Approach

NARCIS (Netherlands)

Lenders, Jos J. M.; Dey, Archan; Bomans, Paul H. H.; Spielmann, Jan; Hendrix, Marco M. R. M.; de With, Gijsbertus; Meldrum, Fiona C.; Harder, Sjoerd; Sommerdijk, Nico A. J. M.

2012-01-01

While biogenic calcites frequently contain appreciable levels of magnesium, the pathways leading to such high concentrations remain unclear. The production of high-magnesian calcites in vitro is highly challenging, because Mg-free aragonite, rather than calcite, is the favored product in the

Ab Initio Study of the Structure and Stability of High-Pressure Iron-Bearing Dolomite

Science.gov (United States)

Solomatova, N. V.; Asimow, P. D.

2016-12-01

Carbon is subducted into the mantle primarily in the form of metasomatically calcium-enriched basaltic rock, calcified serpentinites and carbonaceous ooze, all of which often contain dolomite. End-member CaMg(CO3)2 dolomite typically breaks down upon compression into two carbonates at 5-6 GPa in the temperature range of 800-1200 K [1]. However, high-pressure X-ray diffraction experiments have recently shown that the presence of iron may be sufficient to stabilize high-pressure dolomite over single-cation carbonates above 35 GPa [2,3]. The structure and equation of state of high-pressure dolomite phases have been debated, creating a need for theoretical calculations. Using density functional theory interfaced with a genetic algorithm that predicts crystal structures (USPEX), we have found a monoclinic phase with space group C2/c. The C2/c structure has a lower energy than previously reported dolomite structures at relevant pressures. It is possible that this phase is not achieved experimentally due to a large energy barrier and a correspondingly large required volume drop, resulting in the transformation to metastable dolomite II. We calculate the equation of state of trigonal dolomite, dolomite III and monoclinic C2/c dolomite to 80 GPa with 0 and 50 mol% CaFe(CO3)2 and compare their enthalpies to single-carbonate assemblages. Although end-member C2/c CaMg(CO3)2 dolomite is not stable relative to single-cation carbonates, C2/c CaMg0.5Fe0.5(CO3)2 is preferred over single-cation carbonates at high pressures. Thus, iron-bearing C2/c dolomite may be an important host phase for carbon in slabs subducted into the lower mantle. [1] Shirasaka, M., et al. (2002) American Mineralogist, 87, 922-930. [2] Mao, Z. et al. (2011) Geophysical Research Letters, 38. [3] Merlini, M. et al. (2012) Proceedings of the National Academy of Sciences, 109, 13509-13514.

Uranium and diagenesis in evaporitic lacustrine mudstone of the Oligocene White River Group, Dawes County, Nebraska. Bulletin

International Nuclear Information System (INIS)

Dickinson, K.A.

1991-01-01

The Oligocene White River Group consists of the Chadron and the overlying Brule Formations in northwestern Nebraska. The Chadron Formation consists of alluvial and colluvial vitric mudstone beds, but in addition contains white persistent layers (purplish-white layers) that probably resulted from soil formation on vitric parent material. West of the current study area a basal sandstone facies of the Chadron is host rock for the Crow Butte uranium deposit. The Brule, which consists mostly of pedogenically altered alluvial and fluvial vitric mudstone deposits, contains a uraniferous lacustrine facies northwest of Chadron, Nebraska. Detrital minerals in rocks of the White River Group include quartz, feldspar, volcanic glass, smectite, and illite. Chemical precipitate minerals in the lacustrine facies are calcite, dolomite, and gypsum. Authigenic minerals include calcite, dolomite, gypsum, smectite, opal, chalcedony, together with oxidized uranium minerals

X-ray scattering of calcite thin films deposited by atomic layer deposition: Studies in air and in calcite saturated water solution

Energy Technology Data Exchange (ETDEWEB)

Wang, Peng [Lujan Neutron Scattering Center, Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, NM 87545 (United States); Hudak, Michael R.; Lerner, Allan [Earth and Environmental Sciences Division, Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, NM 87545 (United States); Grubbs, Robert K. [Sandia National Laboratories, P.O. Box 5800, Albuquerque, NM 87185 (United States); Wang, Shanmin [Lujan Neutron Scattering Center, Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, NM 87545 (United States); Zhang, Zhan; Karapetrova, Evguenia [Advance Photon Source, Argonne National Laboratory, 9700S Cass Ave, Argonne, IL 60439 (United States); Hickmott, Donald [Earth and Environmental Sciences Division, Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, NM 87545 (United States); Majewski, Jaroslaw, E-mail: jarek@lanl.gov [Lujan Neutron Scattering Center, Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, NM 87545 (United States)

2014-08-28

Carbonates are one of the most abundant groups of minerals in earth systems and are important in many geological settings and industrial processes. Calcite (CaCO{sub 3}) thin films produced by atomic layer deposition offer a method to evaluate the surficial properties of carbonates as well as interactions at the carbonate–fluid interface. Using synchrotron X-ray reflectivity and X-ray diffraction, these films are observed to be porous, polycrystalline, and have crystallites oriented with the major (104) calcite cleavage plane parallel to the surface of the z-cut single crystal quartz substrate. An Al{sub 2}O{sub 3} buffer layer, present between quartz and the calcite film, does not affect the as-deposited film, but does influence how the films reorganize in contact with fluid. Without a buffer layer, calcite reorients its crystallites to have populations of (006) and (030) parallel to the substrate, while those with an Al{sub 2}O{sub 3} buffer layer become more amorphous. Amorphous films may represent an analog to amorphous calcium carbonate and provide insights into that material's thermophysical behavior. Due to a higher percentage of pore spaces available for fluid infiltration, films deposited at higher temperature make the calcite thin films more susceptible to amorphization. These films are chemically similar, but structurally dissimilar to bulk natural calcite. Nevertheless, they can be a complementary system to traditional single crystal X-ray surface scattering studies on carbonates, particularly for important but less common minerals, to evaluate mineral–fluid interfacial interactions. - Highlights: • Atomic layer deposition (ALD) used to produce calcite films. • Calcite film orientation and crystallinity depend on ALD parameters. • ALD calcite films can be both crystalline and amorphous. • Interaction of water with films can re-orient or amorphize the films. • ALD calcite films may be useful to study carbonate–fluid interfacial

X-ray scattering of calcite thin films deposited by atomic layer deposition: Studies in air and in calcite saturated water solution

International Nuclear Information System (INIS)

Wang, Peng; Hudak, Michael R.; Lerner, Allan; Grubbs, Robert K.; Wang, Shanmin; Zhang, Zhan; Karapetrova, Evguenia; Hickmott, Donald; Majewski, Jaroslaw

2014-01-01

Carbonates are one of the most abundant groups of minerals in earth systems and are important in many geological settings and industrial processes. Calcite (CaCO 3 ) thin films produced by atomic layer deposition offer a method to evaluate the surficial properties of carbonates as well as interactions at the carbonate–fluid interface. Using synchrotron X-ray reflectivity and X-ray diffraction, these films are observed to be porous, polycrystalline, and have crystallites oriented with the major (104) calcite cleavage plane parallel to the surface of the z-cut single crystal quartz substrate. An Al 2 O 3 buffer layer, present between quartz and the calcite film, does not affect the as-deposited film, but does influence how the films reorganize in contact with fluid. Without a buffer layer, calcite reorients its crystallites to have populations of (006) and (030) parallel to the substrate, while those with an Al 2 O 3 buffer layer become more amorphous. Amorphous films may represent an analog to amorphous calcium carbonate and provide insights into that material's thermophysical behavior. Due to a higher percentage of pore spaces available for fluid infiltration, films deposited at higher temperature make the calcite thin films more susceptible to amorphization. These films are chemically similar, but structurally dissimilar to bulk natural calcite. Nevertheless, they can be a complementary system to traditional single crystal X-ray surface scattering studies on carbonates, particularly for important but less common minerals, to evaluate mineral–fluid interfacial interactions. - Highlights: • Atomic layer deposition (ALD) used to produce calcite films. • Calcite film orientation and crystallinity depend on ALD parameters. • ALD calcite films can be both crystalline and amorphous. • Interaction of water with films can re-orient or amorphize the films. • ALD calcite films may be useful to study carbonate–fluid interfacial interactions

Tectonics of the crystalline Basement of the Dolomites in North Italy

NARCIS (Netherlands)

Agterberg, F.P.

1961-01-01

The present thesis deals with a number of crystalline regions around the Dolomites in North Italy. The geographic position is shown on sheet I, which is depicted in fig. 105. The Dolomites proper consist mainly of Permotriassic, overlying a transgression plane, which cuts off the

Extraction of magnesium from calcined dolomite ore using hydrochloric acid leaching

Science.gov (United States)

Royani, Ahmad; Sulistiyono, Eko; Prasetiyo, Agus Budi; Subagja, Rudi

2018-05-01

Magnesium is widely used in varieties industrial sector. Dolomite is one source of magnesium besides seawater. The extraction of magnesium from dolomite ores can be done by leaching process. In this work, the dolomite leaching to extract magnesium by hydrochloric acid was investigated. The leaching experiments were performed in a spherical glass batch reactor having a capacity of 1000 ml. The effects of the stirring speed, acid concentration, reaction temperature and liquid-solid ratio for each reaction time of 1; 2; and 3 h on the Mg leaching have been evaluated. 5 ml of solution sample were collected from the leached solutions, then it was filtered prior to analysis by ICP OES. The experimental results show that the magnesium extraction increases along with the increase of acid concentration, liquid-solid ratio and temperature. The optimum conditions for magnesium extraction were achieved at temperature 75 °C, extraction time 3 h, the HCl concentration of 2 M, the liquid-solid ratio 20 ml/g and stirring speed of 400 rpm. At this condition 98, 82 % of magnesium were extracted from dolomite. The conclusion obtained from this leaching process is that the magnesium can be extracted from dolomite by using hydrochloric acid solutions.

Is bicarbonate stable in and on the calcite surface?

Science.gov (United States)

Andersson, M. P.; Rodriguez-Blanco, J. D.; Stipp, S. L. S.

2016-03-01

We have used density functional theory with the COSMO-RS implicit solvent model to predict the pKa for the deprotonation of bicarbonate to carbonate, i.e. HCO3- CO32- + H+, when HCO3- is included in, and adsorbed on, a calcite surface. We have used cluster models (80-100 atoms) to represent the flat {10.4} surface, acute steps, obtuse steps, two types of kinks on the acute step and two types of kinks on the obtuse steps. Based on the predicted pKa values, which range from -6.0 to 2.4 depending on the surface site, we conclude that bicarbonate deprotonates to carbonate when it is in calcite even when pH in solution is very low. This is true for all surface sites, even for solutions where 2.4 < pH < 6.35, where H2CO30 is the dominant dissolved species. When bicarbonate is adsorbed on calcite, the predicted pKa for deprotonation is 7.5, which is ∼3 pH units lower than in aqueous solution, 10.35. This means that adsorbed carbonate is stable even when the concentration of dissolved CO32- is several orders of magnitude lower. This has a significant effect on surface charge and thus the behaviour of the calcite surface. Our results help explain the potential determining behaviour of the carbonate species in calcite-water systems, particularly in the pH range where the bicarbonate species dominates in water and where the carbonate species dominates at the surface, i.e. when 7.5 < pH < 10.35. Our atomic scale data for the various calcite surface sites provide the needed input to improve and constrain surface complexation modelling and are especially useful for predicting behaviour in systems where experiments are difficult or impossible, such as at high temperature and pressure.

Calcite surface structure and reactivity: molecular dynamics simulations and macroscopic surface modelling of the calcite-water interface

NARCIS (Netherlands)

Wolthers, M.; Di Tommaso, D.; Du, Z.; de Leeuw, N.H.

2012-01-01

Calcite–water interactions are important not only in carbon sequestration and the global carbon cycle, but also in contaminant behaviour in calcite-bearing host rock and in many industrial applications. Here we quantify the effect of variations in surface structure on calcite surface reactivity.

Tectonics of the crystalline Basement of the Dolomites in North Italy

NARCIS (Netherlands)

Agterberg, F.P.

1961-01-01

The present thesis deals with a number of crystalline regions around the Dolomites in North Italy. The geographic position is shown on sheet I, which is depicted in fig. 105. The Dolomites proper consist mainly of Permotriassic, overlying a transgression plane, which cuts off the studied crystalline

Important geosites and parks in the UNESCO World Heritage Site of the Dolomites

International Nuclear Information System (INIS)

Nossing, L.; Forti, S.

2016-01-01

In the geological complexity of the south Tyrol, the Dolomites play a fundamental role, as they are now included in the UNESCO World Heritage (2009) because of their exceptional beauty and unique landscape, together with numerous scientific discoveries. The name of Dolomite comes from the famous mineral dolomite (double calcium magnesium carbonate) discovered by Déodat De Dolomieu in 1789. The dolomitic rocks constitute a large area of the Triassic mountains and many studies have contributed to the discovery of the fundamental stratotypes for the signature of the Permian/Triassic boundary. The steep walls of the Permian volcanic formations and the Sciliar Mountain have always been a great attraction for scientists from all over the world to study the open book of nature in the Dolomites. We will illustrate three sites: 1. The Bula Geotrail. A geological trail through one of the best-preserved sedimentary series in which we can observe one of the most important stratotypes to touch the Permian/Triassic boundary. 2. The Siusi-Alpe di Siusi Geological Trail. This trail starts just above the Permian/Triassic boundary and is characterized by some unique basaltic columnar formations and other significant outcrops of Lower and Medium Triassic. 3. The Bletterbach Geopark. In this sequence the stratotype, which represents the boundary, is a dark coloured continuous layer (organic matter) 5cm thick, and contains some paleobotanical evidence which is unique in the world. The preservation and added value of the natural and geological patrimony of a region through guided and documented trails are at the origin of a new kind of tourism: geotourism. The modern tourist is more and more interested and stimulated by getting to knowing nature in depth. The trails are the best instruments for scientific divulgation and education, allowing a better understanding of the landscape and stimulating new discoveries. (Author)

Important geosites and parks in the UNESCO World Heritage Site of the Dolomites

Energy Technology Data Exchange (ETDEWEB)

Nossing, L.; Forti, S.

2016-10-01

In the geological complexity of the south Tyrol, the Dolomites play a fundamental role, as they are now included in the UNESCO World Heritage (2009) because of their exceptional beauty and unique landscape, together with numerous scientific discoveries. The name of Dolomite comes from the famous mineral dolomite (double calcium magnesium carbonate) discovered by Déodat De Dolomieu in 1789. The dolomitic rocks constitute a large area of the Triassic mountains and many studies have contributed to the discovery of the fundamental stratotypes for the signature of the Permian/Triassic boundary. The steep walls of the Permian volcanic formations and the Sciliar Mountain have always been a great attraction for scientists from all over the world to study the open book of nature in the Dolomites. We will illustrate three sites: 1. The Bula Geotrail. A geological trail through one of the best-preserved sedimentary series in which we can observe one of the most important stratotypes to touch the Permian/Triassic boundary. 2. The Siusi-Alpe di Siusi Geological Trail. This trail starts just above the Permian/Triassic boundary and is characterized by some unique basaltic columnar formations and other significant outcrops of Lower and Medium Triassic. 3. The Bletterbach Geopark. In this sequence the stratotype, which represents the boundary, is a dark coloured continuous layer (organic matter) 5cm thick, and contains some paleobotanical evidence which is unique in the world. The preservation and added value of the natural and geological patrimony of a region through guided and documented trails are at the origin of a new kind of tourism: geotourism. The modern tourist is more and more interested and stimulated by getting to knowing nature in depth. The trails are the best instruments for scientific divulgation and education, allowing a better understanding of the landscape and stimulating new discoveries. (Author)

Strontium Incorporation into Calcite Generated by Bacterial Ureolysis

International Nuclear Information System (INIS)

Yoshiko Fujita; George D. Redden; Jani C. Ingram; Marnie M. Cortez; Robert W. Smith

2004-01-01

Strontium incorporation into calcite generated by bacterial ureolysis was investigated as part of an assessment of a proposed remediation approach for 90Sr contamination in groundwater. Urea hydrolysis produces ammonium and carbonate and elevates pH, resulting in the promotion of calcium carbonate precipitation. Urea hydrolysis by the bacterium Bacillus pasteurii in a medium designed to mimic the chemistry of the Snake River Plain Aquifer in Idaho resulted in a pH rise from 7.5 to 9.1. Measured average distribution coefficients (DEX) for Sr in the calcite produced by ureolysis (0.5) were up to an order of magnitude higher than values reported in the literature for natural and synthetic calcites (0.02-0.4). They were also higher than values for calcite produced abiotically by ammonium carbonate addition (0.3). The precipitation of calcite in these experiments was verified by X-ray diffraction. Time-of-flight secondary ion mass spectrometry (ToF SIMS) depth profiling (up to 350 nm) suggested that the Sr was not merely sorbed on the surface, but was present at depth within the particles. X-ray absorption near edge spectra showed that Sr was present in the calcite samples as a solid solution. The extent of Sr incorporation appeared to be driven primarily by the overall rate of calcite precipitation, where faster precipitation was associated with greater Sr uptake into the solid. The presence of bacterial surfaces as potential nucleation sites in the ammonium carbonate precipitation treatment did not enhance overall precipitation or the Sr distribution coefficient. Because bacterial ureolysis can generate high rates of calcite precipitation, the application of this approach is promising for remediation of 90Sr contamination in environments where calcite is stable over the long term

Fracture calcites at Olkiluoto. Evidence from quaternary infills for palaeohydrogeology

International Nuclear Information System (INIS)

Gehoer, S.; Kaerki, A.; Taikina-aho, O.; Karhu, J.; Loefman, J.; Pitkaenen, P.; Ruotsalainen, P.

2002-02-01

Recently formed secondary minerals, predominantly calcite, occur in varying amounts as fracture infills, and the calcite types, their chemical compositions and isotope ratios reflect the compositions and physicochemical factors of the groundwater system in which they were formed. Fluid inclusions trapped in calcites give direct evidence of trapping temperatures and past salinities and of the chemical compositions of the palaeo fluids. A wide range of mineralogical and geochemical examinations were carried out within the EQUIP project to examine features of this kind. The fracture calcites at the Olkiluoto site are of various origins and represent several textural types. The exact number of calcite-producing events is unknown, but the duration of the period that was appropriate for the precipitation of low temperature calcite is estimated to have exceeded 1000 Ma. Thus the number of genetically related calcite units is assumed to be considerable. This study was focused on the petrogenesis of calcites crystallized in fractures of high water conductivity during the latest stages of geological evolution. The majority of these late stage calcites form physically homogeneous, scaly layers, and in a few cases thin layers composed of idiomorphic crystals. Chemically these are almost stoichiometric calcites (CaCO 3 ). The MnO content may exceed 1%, while the amounts of other elements present are minor, although the trace element concentrations, particularly those of large ionic trace elements, can be used as distinguishing features for the recognition of individual precipitates representing different calcite generations. Evidence from fluid inclusions, or more correctly from the absence of these in the late stage calcites, can be interpreted as an indication of slow rates of crystallization under cool conditions. Many chemical variables, e.g. oxygen isotope ratios, demonstrate an equilibrium between the latest calcites and water similar to the present groundwater. Older

Fracture calcites at Olkiluoto. Evidence from quaternary infills for palaeohydrogeology

Energy Technology Data Exchange (ETDEWEB)

Gehoer, S.; Kaerki, A.; Taikina-aho, O. [Kivitieto Oy (Finland); Karhu, J. [Helsinki Univ. (Finland); Loefman, J. [VTT Processes, Espoo (Finland); Pitkaenen, P. [VTT Building and Transport, Espoo (Finland); Ruotsalainen, P. [TUKES, Helsinki (Finland)

2002-02-01

Recently formed secondary minerals, predominantly calcite, occur in varying amounts as fracture infills, and the calcite types, their chemical compositions and isotope ratios reflect the compositions and physicochemical factors of the groundwater system in which they were formed. Fluid inclusions trapped in calcites give direct evidence of trapping temperatures and past salinities and of the chemical compositions of the palaeo fluids. A wide range of mineralogical and geochemical examinations were carried out within the EQUIP project to examine features of this kind. The fracture calcites at the Olkiluoto site are of various origins and represent several textural types. The exact number of calcite-producing events is unknown, but the duration of the period that was appropriate for the precipitation of low temperature calcite is estimated to have exceeded 1000 Ma. Thus the number of genetically related calcite units is assumed to be considerable. This study was focused on the petrogenesis of calcites crystallized in fractures of high water conductivity during the latest stages of geological evolution. The majority of these late stage calcites form physically homogeneous, scaly layers, and in a few cases thin layers composed of idiomorphic crystals. Chemically these are almost stoichiometric calcites (CaCO{sub 3}). The MnO content may exceed 1%, while the amounts of other elements present are minor, although the trace element concentrations, particularly those of large ionic trace elements, can be used as distinguishing features for the recognition of individual precipitates representing different calcite generations. Evidence from fluid inclusions, or more correctly from the absence of these in the late stage calcites, can be interpreted as an indication of slow rates of crystallization under cool conditions. Many chemical variables, e.g. oxygen isotope ratios, demonstrate an equilibrium between the latest calcites and water similar to the present groundwater. Older

An investigation of the heterogeneous nucleation of calcite

International Nuclear Information System (INIS)

House, W.A.; Tutton, J.A.

1982-01-01

The heterogeneous precipitation kinetics of calcite from dilute calcium bicarbonate solutions onto pyrex glass seeds is investigated by using a modified form of the Davies and Jones equation. The rate constant is evaluated from experiments using calcite seeds and it is demonstrated that the growth rate does not increase in proportion to the increase in surface area accompanying precipitation. The number of heteronucleated particles is estimated by assuming a constant density of growth sites on the different calcite surfaces. A comparison is made between the specific surface areas of calcite obtained by the calcium-45 isotopic exchange method and other values. (orig.)

Dissolution of coccolithophorid calcite by microzooplankton and copepod grazing

Science.gov (United States)

Antia, A. N.; Suffrian, K.; Holste, L.; Müller, M. N.; Nejstgaard, J. C.; Simonelli, P.; Carotenuto, Y.; Putzeys, S.

2008-01-01

Independent of the ongoing acidification of surface seawater, the majority of the calcium carbonate produced in the pelagial is dissolved by natural processes above the lysocline. We investigate to what extent grazing and passage of coccolithophorids through the guts of copepods and the food vacuoles of microzooplankton contribute to calcite dissolution. In laboratory experiments where the coccolithophorid Emiliania huxleyi was fed to the rotifer Brachionus plicatilis, the heterotrophic flagellate Oxyrrhis marina and the copepod Acartia tonsa, calcite dissolution rates of 45-55%, 37-53% and 5-22% of ingested calcite were found. We ascribe higher loss rates in microzooplankton food vacuoles as compared to copepod guts to the strongly acidic digestion and the individual packaging of algal cells. In further experiments, specific rates of calcification and calcite dissolution were also measured in natural populations during the PeECE III mesocosm study under differing ambient pCO2 concentrations. Microzooplankton grazing accounted for between 27 and 70% of the dynamic calcite stock being lost per day, with no measurable effect of CO2 treatment. These measured calcite dissolution rates indicate that dissolution of calcite in the guts of microzooplankton and copepods can account for the calcite losses calculated for the global ocean using budget and model estimates.

Thermoluminescence from natural calcites

International Nuclear Information System (INIS)

Calderon, T.; Jaque, F.; Coy-yll, R.

1984-01-01

Thermoluminescence (TL) as well as absorption and EPR spectra of x-irradiated natural calcites have been obtained. Irradiation produces UV absorption bands and a decrease of the Mn 2+ EPR spectrum. A correlation of each TL peak with the bleaching steps of UV absorption bands and the recovering in intensity of the Mn 2+ EPR spectrum has been found. These experimental results support a new model for the radiation damage and thermoluminescence process in calcites. The main point in this model is that holes become trapped at impurities, and the electrons are trapped at dislocations in the form of CO 3 3- . (author)

The role of silicate surfaces on calcite precipitation kinetics

DEFF Research Database (Denmark)

Stockmann, Gabrielle J.; Wolff-Boenisch, Domenik; Bovet, Nicolas Emile

2014-01-01

The aim of this study is to illuminate how calcite precipitation depends on the identity and structure of the growth substrate. Calcite was precipitated at 25°C from supersaturated aqueous solutions in the presence of seeds of either calcite or one of six silicate materials: augite, enstatite......, labradorite, olivine, basaltic glass and peridotite rock. Calcite saturation was achieved by mixing a CaCl2-rich aqueous solution with a NaHCO3-Na2CO3 aqueous buffer in mixed-flow reactors containing 0.5-2g of mineral, rock, or glass seeds. This led to an inlet fluid calcite saturation index of 0.6 and a p...

Is bicarbonate stable in and on the calcite surface?

DEFF Research Database (Denmark)

Andersson, Martin Peter; Rodriguez Blanco, Juan Diego; Stipp, Susan Louise Svane

2016-01-01

We have used density functional theory with the COSMO-RS implicit solvent model to predict the pKa for the deprotonation of bicarbonate to carbonate, i.e. HCO3− CO32− + H+, when HCO3− is included in, and adsorbed on, a calcite surface. We have used cluster models (80–100 atoms) to represent...... the flat {10.4} surface, acute steps, obtuse steps, two types of kinks on the acute step and two types of kinks on the obtuse steps. Based on the predicted pKa values, which range from −6.0 to 2.4 depending on the surface site, we conclude that bicarbonate deprotonates to carbonate when it is in calcite...... even when pH in solution is very low. This is true for all surface sites, even for solutions where 2.4 bicarbonate is adsorbed on calcite, the predicted pKa for deprotonation is 7.5, which is ∼3 pH units lower than in aqueous solution...

Mineralogical-Chemical Characteristics of Calcite from Zletovo, Sasa and Buchim Deposits

International Nuclear Information System (INIS)

Shijakova-lvanova, Tena; Paneva-Zajkova, Vesna; Donova, Ilinka

2006-01-01

The paper presents mineralogical-chemical characteristics, dependence between some elements and concentration of some calcite elements of Zletovo, Sasa and Buchim deposits. Calcite from Sasa, Zletovo and Buchim occurs in rhombohedral crystals of different size. The colour is white, but in Buchim it is white, pink, and yellow. Their twinning is very common. Chemical composition of calcite was determined by AES-ICP. Results show that in calcite from Buchim the concentration of Ba is much higher in pink calcite from than in white or yellow. The concentration of Zn and Ph is the lowest in white calcite. The calcite from Zletovo contains much higher concentrations of Pb, Zn, Sr, but calcite of Buchim which is pink contains higher amounts of Ba and Co. The concentrations of CaO, MgO, and MnO in all calcite simples are approximately equal. Concentration of all other elements in calcite of Sasa, Zletovo and Buchim is approximately equal. TG and DTA curves out on all simples were recorded.The decompositions of the samples of calcite starts at different temperature and it is not finish until 1000 o C. (Author)

Calcite growth kinetics: Modeling the effect of solution stoichiometry

NARCIS (Netherlands)

Wolthers, M.; Nehrke, G.; Gustafsson, J.P.; Van Cappellen, P.

2012-01-01

Until recently the influence of solution stoichiometry on calcite crystal growth kinetics has attracted little attention, despite the fact that in most aqueous environments calcite precipitates from non-stoichiometric solution. In order to account for the dependence of the calcite crystal growth

Biolaminoid facies in a peritidal sabkha: Permian Platy Dolomite of northern Poland

Science.gov (United States)

Brehm, Ulrike; Gasiewicz, Andreij; Gerdes, Giesela; Krumbein, Wolfgang

The Platy Dolomite, a carbonate unit in the Zechstein Formation (Upper Permian) of the Leba Elevation, Poland, was deposited in a semi-closed or completely separated back-barrier sabkha environment. This arid, hypersaline zone is comparable to the recent Gavish Sabkha, Sinai. The processes which formed the modern Gavish Sabkha are similar to those responsible for the biolaminoid formation in the Platy Dolomite series. The deposition of this Platy Dolomite was mainly the result of microbial activity building extensive microbial mats. The Platy Dolomite is characterized by loosely packed microbial biolaminoids (a less significantly laminated build-up of biogenetic sediments) with horizontally or obliquely to vertically orientated filaments. Intermediary coated grains occur. Densely packed, flat laminated stromatolitic rocks, pure oolites, and bioclastic sedimentary strata are rarely intercalated with the biolaminoid beds. Laboratory and field investigations indicate that carbonate formation was induced by the chemoorganotrophic bacterial decay of cyanobacterial mats. Magnesium was bound and absorbed by organic matter and later liberated by anaerobic decay. Early diagenetic processes formed Mg2+- and Ca2+-enriched solutions in which carbonates precipitated biologically and chemically. A system of biogenic carbonate formation of the Platy Dolomite microbiolite series is proposed and supported by the results of microbiological laboratory studies.

The influence of petrography, mineralogy and chemistry on burnability and reactivity of quicklime produced in Twin Shaft Regenerative (TSR) kilns from Neoarchean limestone (Transvaal Supergroup, South Africa)

Science.gov (United States)

Vola, Gabriele; Sarandrea, Luca; Della Porta, Giovanna; Cavallo, Alessandro; Jadoul, Flavio; Cruciani, Giuseppe

2017-12-01

This study evaluates the influence of chemical, mineralogical and petrographic features of the Neoarchean limestone from the Ouplaas Mine (Griqualand West, South Africa) on its burnability and quicklime reactivity, considering the main use as raw material for high-grade lime production in twin shaft regenerative (TSR) kilns. This limestone consists of laminated clotted peloidal micrite and fenestrate microbial boundstone with herringbone calcite and organic carbon (kerogen) within stylolites. Diagenetic modifications include hypidiotopic dolomite, micrite to microsparite recrystallization, stylolites, poikilotopic calcite, chert and saddle dolomite replacements. Burning and technical tests widely attest that the Neoarchean limestone is sensitive to high temperature, showing an unusual and drastically pronounced sintering or overburning tendency. The slaking reactivity, according to EN 459-2 is high for lime burnt at 1050 °C, but rapidly decreases for lime burnt at 1150 °C. The predominant micritic microbial textures, coupled with the organic carbon, are key-factors influencing the low burnability and the high sintering tendency. The presence of burial cementation, especially poikilotopic calcite, seems to promote higher burnability, either in terms of starting calcination temperature, or in terms of higher carbonate dissociation rate. In fact, the highest calcination velocity determined by thermal analysis is consistent with the highest slaking reactivity of the lower stratum of the quarry, enriched in poikilotopic calcite. Secondly, locally concentered dolomitic marly limestones, and sporadic back shales negatively affects the quicklime reactivity, as well. This study confirms that a multidisciplinary analytical approach is essential for selecting the best raw mix for achieving the highest lime reactivity in TSR kilns.

Atom-resolved AFM imaging of calcite nanoparticles in water

Energy Technology Data Exchange (ETDEWEB)

Imada, Hirotake; Kimura, Kenjiro [Department of Chemistry, School of Science, Kobe University, Rokko-dai, Nada, Kobe 657-8501 (Japan); Onishi, Hiroshi, E-mail: oni@kobe-u.ac.jp [Department of Chemistry, School of Science, Kobe University, Rokko-dai, Nada, Kobe 657-8501 (Japan)

2013-06-20

Highlights: ► An advanced frequency-modulation AFM (FM-AFM) was applied for imaging particles. ► Atom-resolved topography of nano-sized particles of calcite was observed in water. ► Locally ordered structures were found and assigned to a (104) facet of calcite. ► A promising ability of FM-AFM was demonstrated in imaging nano-sized particles. - Abstract: The atom-resolved topography of calcite nanoparticles was observed in water using a frequency-modulation atomic force microscope. Locally ordered structures were found and assigned to a (104) facet of crystalline calcite.

Atom-resolved AFM imaging of calcite nanoparticles in water

International Nuclear Information System (INIS)

Imada, Hirotake; Kimura, Kenjiro; Onishi, Hiroshi

2013-01-01

Highlights: ► An advanced frequency-modulation AFM (FM-AFM) was applied for imaging particles. ► Atom-resolved topography of nano-sized particles of calcite was observed in water. ► Locally ordered structures were found and assigned to a (104) facet of calcite. ► A promising ability of FM-AFM was demonstrated in imaging nano-sized particles. - Abstract: The atom-resolved topography of calcite nanoparticles was observed in water using a frequency-modulation atomic force microscope. Locally ordered structures were found and assigned to a (104) facet of crystalline calcite

Empirical Calibration for Dolomite Stoichiometry Calculation: Application on Triassic Muschelkalk- Lettenkohle Carbonates (French Jura Calibration empirique pour le calcul de la stoechiométrie de la dolomite : application aux carbonates triasiques du Muschelkalk-Lettenkohle (Jura français

Directory of Open Access Journals (Sweden)

Turpin M.

2012-02-01

Full Text Available This study concerns an approach for dolomite quantification and stoichiometry calculation by using X-ray diffractometry coupled with cell and Rietveld refinements and equipped with a newly substantial database of dolomite composition. A greater accuracy and precision are obtained for quantifying dolomite as well as other mineral phases and calculating dolomite stoichiometry compared to the classical “Lumsden line” and previous methods. The applicability of this approach is verified on dolomite reference material (Eugui and on Triassic (Upper Muschelkalk-Lettenkohle carbonates from the French Jura. The approach shown here is applicable to bulk dolostones as well as to specific dolomite cements and was combined with petrographical and isotopic analyses. Upper Muschelkalk dolomites were formed during burial dolomitization under fluids characterized by increased temperature and variable isotopic composition through burial. This is clear from their Ca content in dolomites which gradually approaches an ideal stoichiometry (from 53.16% to 51.19% through increasing dolomitization. Lettenkohle dolostones consist of near-ideal stoichiometric (51.06%Ca and well-ordered dolomites associated with anhydrite relicts. They originated through both sabkha and burial dolomitization. This contribution gives an improved method for the characterization of different dolomite types and their distinct traits in sedimentary rocks, which allows a better evaluation of their reservoir potential. Cette étude propose une approche pour la quantification de la dolomite et le calcul de sa stoechiométrie grâce à l’utilisation de la diffraction des rayons X couplée aux affinements de maille et de Rietveld et complétée par de nombreuses données issues de la littérature. Elle permet d’obtenir une meilleure justesse et précision pour la quantification de la dolomite (et des autres phases minérales ainsi que pour le calcul de sa stoechiométrie par rapport à l�

Downflow limestone beds for treatment of net-acidic, oxic, iron-laden drainage from a flooded anthracite mine, Pennsylvania, USA: 2. Laboratory evaluation

Science.gov (United States)

Cravotta, C.A.; Ward, S.J.; Hammarstrom, J.M.

2008-01-01

Acidic mine drainage (AMD) containing elevated concentrations of dissolved iron and other metals can be neutralized to varying degrees by reactions with limestone in passive treatment systems. We evaluated the chemical and mineralogical characteristics and the effectiveness of calcitic and dolomitic limestone for the neutralization of net-acidic, oxic, iron-laden AMD from a flooded anthracite mine. The calcitic limestone, with CaCO3 and MgCO3 contents of 99.8 and treatment system in 2003 at the Bell Mine, a large source of AMD and baseflow to the Schuylkill River in the Southern Anthracite Coalfield, in east-central Pennsylvania. In the winter of 2002-2003, laboratory neutralization-rate experiments evaluated the evolution of effluent quality during 2 weeks of continuous contact between AMD from the Bell Mine and the crushed calcitic or dolomitic limestone in closed, collapsible containers (cubitainers). The cubitainer tests showed that: (1) net-alkaline effluent could be achieved with detention times greater than 3 h, (2) effluent alkalinities and associated dissolution rates were equivalent for uncoated and Fe(OH)3-coated calcitic limestone, and (3) effluent alkalinities and associated dissolution rates for dolomitic limestone were about half those for calcitic limestone. The dissolution rate data for the cubitainer tests were used with data on the volume of effuent and surface area of limestone in the treatment system at the Bell Mine to evaluate the water-quality data for the first 1.5 years of operation of the treatment system. These rate models supported the interpretation of field results and indicated that treatment benefits were derived mainly from the dissolution of calcitic limestone, despite a greater quantity of dolomitic limestone within the treatment system. The dissolution-rate models were extrapolated on a decadal scale to indicate the expected decreases in the mass of limestone and associated alkalinities resulting from the long-term reaction of

Telescoped porphyry-style and epithermal veins and alteration at the central Maratoto valley prospect, Hauraki Goldfield, New Zealand

International Nuclear Information System (INIS)

Simpson, M.P.; Mauk, J.L.; Kendrick, R.G.

2004-01-01

At the central Maratoto valley prospect, southern Coromandel Peninsula, New Zealand, andesite flows and dacite breccias host rare porphyry-style quartz veins that are telescoped by widespread epithermal veins and alteration. Early porphyry-style quartz veins, which lack selvages of porphyry-style alteration, host hypersaline fluid inclusions that contain several translucent daughter crystals, including halite and sylvite. Overprinting epithermal veins and alteration are divided into two stages. Main-stage epithermal alteration and veins are characterised by the successive deposition of pyrite, quartz, and ankerite-dolomite veinlets coupled with intense alteration of the wall rock to quartz, illite, interlayer illite-smectite (≤ 10% smectite), chlorite, pyrite, ankerite, and dolomite. Late-stage epithermal veins and alteration are characterised by the formation of calcite and siderite veinlets, coupled with overprinting of the wall rocks by both these minerals. Multiphase fluid inclusions in a porphyry-style quartz vein formed at temperatures >400 degrees C and trapped hypersaline magmatic fluid. Lower temperature secondary liquid-rich inclusions in the porphyry-style quartz vein homogenise between 283 and 329 degrees C and trapped a dilute fluid with 18 O (VSMOW) values of 13.5-18.1 permille, whereas late-stage epithermal calcite has δ 18 O (VSMOW) values of 3.1-5.1 permille. Calculated isotopic compositions for the fluid in equilibrium with ankerite-dolomite and calcite at 260 degrees C, averages 6 and -3 permille, respectively. The enriched value for main-stage ankerite-dolomite suggests formation from waters that underwent significant water-rock exchange, whereas isotopically lighter water that formed late-stage calcite underwent little water-rock interaction. We propose a three-stage model to explain telescoped veins and alteration styles at the central Maratoto valley prospect area. Porphyry-style quartz veins were the first to form from hot hypersaline

NMR characterization of hydrocarbon adsorption on calcite surfaces: A first principles study

Energy Technology Data Exchange (ETDEWEB)

Bevilaqua, Rochele C. A.; Miranda, Caetano R. [Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, UFABC, Santo André, SP (Brazil); Rigo, Vagner A. [Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, UFABC, Santo André, SP (Brazil); Universidade Tecnológica Federal do Paraná, UTFPR, Cornélio Procópio, PR (Brazil); Veríssimo-Alves, Marcos [Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, UFABC, Santo André, SP (Brazil); Departamento de Física, ICEx, Universidade Federal Fluminense, UFF, Volta Redonda, RJ (Brazil)

2014-11-28

The electronic and coordination environment of minerals surfaces, as calcite, are very difficult to characterize experimentally. This is mainly due to the fact that there are relatively few spectroscopic techniques able to detect Ca{sup 2+}. Since calcite is a major constituent of sedimentary rocks in oil reservoir, a more detailed characterization of the interaction between hydrocarbon molecules and mineral surfaces is highly desirable. Here we perform a first principles study on the adsorption of hydrocarbon molecules on calcite surface (CaCO{sub 3} (101{sup ¯}4)). The simulations were based on Density Functional Theory with Solid State Nuclear Magnetic Resonance (SS-NMR) calculations. The Gauge-Including Projector Augmented Wave method was used to compute mainly SS-NMR parameters for {sup 43}Ca, {sup 13}C, and {sup 17}O in calcite surface. It was possible to assign the peaks in the theoretical NMR spectra for all structures studied. Besides showing different chemical shifts for atoms located on different environments (bulk and surface) for calcite, the results also display changes on the chemical shift, mainly for Ca sites, when the hydrocarbon molecules are present. Even though the interaction of the benzene molecule with the calcite surface is weak, there is a clearly distinguishable displacement of the signal of the Ca sites over which the hydrocarbon molecule is located. A similar effect is also observed for hexane adsorption. Through NMR spectroscopy, we show that aromatic and alkane hydrocarbon molecules adsorbed on carbonate surfaces can be differentiated.

Optimasi Dosis Pupuk Dolomit pada Tanaman Kelapa Sawit (Elaeis Guineensis Jacq. Belum Menghasilkan Umur Satu Tahun

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- Sudradjat

2015-09-01

Full Text Available Kelapa sawit merupakan komoditi perkebunan utama karena sebagai sumber devisa negara dan menyediakan lapangan kerja. Indonesia adalah negara produsen terbesar kelapa sawit di dunia dengan luas areal mencapai 10.1 juta hektar. Peningkatan produktivitas dicapai dengan intensifikasi antara lain dengan melakukan rasionalisasi pemupkan. Penelitian ini bertujuan untuk menentukan dosis optimum pupuk dolomit pada tanaman kelapa sawit belum menghasilkan umur satu tahun. Penelitian ini dilaksanakan di Kebun Pendidikan dan Penelitian Kelapa Sawit IPB-Cargill, Jonggol, Bogor dari bulan Maret 2013 sampai Maret 2014. Rancangan yang digunakan adalah Faktorial Tunggal,  dosis pupuk dolomit,  yang disusun dalam lingkungan Acak Kelompok dengan tiga ulangan. Dosis pupuk dolomit yang diuji  terdiri atas 0, 200, 400, dan 600 g tanaman-1 tahun-1. Hasil penelitian menunjukkan bahwa pupuk dolomit meningkatkan secara nyata terhadap peubah tinggi tanaman, diameter batang, jumlah daun, dan kandungan khlorofil daun, namun tidak berpengaruh terhadap kandungan Mg dalam jaringan daun. Berdasarkan tanggap peubah tinggi tanaman, dosis optimum pupuk dolomit untuk tanaman kelapa sawit pada umur satu tahun adalah 306.4 g dolomit tanaman-1tahun -1. Kata kunci: dolomit, dosis optimum, kelapa sawit, respons fisiologi, respons morfologi.

Rate of radiocarbon retention onto calcite by isotope exchange

Energy Technology Data Exchange (ETDEWEB)

Lempinen, Janne; Lehto, Jukka [Helsinki Univ. (Finland). Lab. of Radiochemistry

2016-11-01

Radiocarbon ({sup 14}C) is a top priority class radionuclide associated with the long-term safety of spent nuclear fuel disposal. Dissolved inorganic radiocarbon can be retained in bedrock via isotope exchange with calcite (CaCO{sub 3}) at solubility equilibrium with groundwater. In the present study, the rate of the isotope exchange process was investigated on synthetic calcite using batch experiments. Experiments were performed in solutions with a calcium concentration of 0.0002-0.1 M, including two synthetic reference groundwaters. The radiocarbon activity in the solutions decreased exponentially as a function of time, thus following first-order kinetics. The rate of isotope exchange was quantified from an exponential fit to the activity data over time. The rate of radiocarbon retention increased as a function of the calcium activity. The isotope exchange half-life was only 4.3 days at calcium ion activities over 0.01. This half-life is very much shorter than the half-life of {sup 14}C or the time scale of groundwater movements; consequently calcite can effectively retain radiocarbon from brackish and saline groundwaters.

Rate of radiocarbon retention onto calcite by isotope exchange

International Nuclear Information System (INIS)

Lempinen, Janne; Lehto, Jukka

2016-01-01

Radiocarbon ( 14 C) is a top priority class radionuclide associated with the long-term safety of spent nuclear fuel disposal. Dissolved inorganic radiocarbon can be retained in bedrock via isotope exchange with calcite (CaCO 3 ) at solubility equilibrium with groundwater. In the present study, the rate of the isotope exchange process was investigated on synthetic calcite using batch experiments. Experiments were performed in solutions with a calcium concentration of 0.0002-0.1 M, including two synthetic reference groundwaters. The radiocarbon activity in the solutions decreased exponentially as a function of time, thus following first-order kinetics. The rate of isotope exchange was quantified from an exponential fit to the activity data over time. The rate of radiocarbon retention increased as a function of the calcium activity. The isotope exchange half-life was only 4.3 days at calcium ion activities over 0.01. This half-life is very much shorter than the half-life of 14 C or the time scale of groundwater movements; consequently calcite can effectively retain radiocarbon from brackish and saline groundwaters.

Study of reverse flotation of calcite from scheelite in acidic media

Science.gov (United States)

Deng, Rongdong; Huang, Yuqing; Hu, Yuan; Ku, Jiangang; Zuo, Weiran; Yin, Wanzhong

2018-05-01

A new coated-reactive reverse flotation method based on the generation of CO2 bubbles at a calcite surface in acidic solution was used to separate calcite from scheelite. The dissolution kinetics of coated and uncoated calcite were studied in sulfuric acid. The CO2 bubbles generated on the uncoated calcite particle surface are enough to float the particle. However, most of these bubbles left the surface quickly, preventing calcite from floating. Here, a mixture of polyvinyl alcohol polymer and sodium dodecyl sulfonate was used to coat the mineral particles and form a stable membrane, resulting in the formation of a stable foam layer on the calcite surface. After the calcite is coated, the generated bubbles could be successfully captured on the calcite surface, and calcite particles could float to the air-water interface and remain there for more than one hour. Flotation tests indicated that a high-quality tungsten concentrate with a grade of more than 75% and a recovery of more than 99% could be achieved when the particle size was between 0.3 and 1.5 mm. The present results provide theoretical support for the development of a highly efficient flotation separation for carbonate minerals.

Effect of Mica and Hematite (001 Surfaces on the Precipitation of Calcite

Directory of Open Access Journals (Sweden)

Huifang Xu

2018-01-01

Full Text Available The substrate effect of mica and hematite on the nucleation and crystallization of calcite was investigated using scanning electron microscope (SEM, X-ray diffraction (XRD, and electron backscatter diffraction (EBSD methods. On mica, we found, in the absence of Mg2+, the substrates’ (001 surfaces with hexagonal and pseudo-hexagonal two-dimensional (2-D structure can affect the orientation of calcite nucleation with calcite (001 ~// mica (001 and calcite (010 ~// mica (010 to be the major interfacial relationship. On hematite, we did not observe frequent twinning relationship between adjacent calcite gains, but often saw preferentially nucleation of calcite at surface steps on hematite substrate. We suggest that calcite crystals initially nucleate from the Ca2+ layers adsorbed on the surfaces. The pseudo-hexagonal symmetry on mica (001 surface also leads to the observed calcite (001 twinning. A second and less common orientation between calcite {104} and mica (001 was detected but could be due to local structure damage of the mica surface. Results in the presence of Mg2+ show that the substrate surfaces can weaken Mg toxicity to calcite nucleation and lead to a higher level of Mg incorporation into calcite lattice.

Petrophysics of shale intervals in the Skjold Field, Danish North Sea

DEFF Research Database (Denmark)

Mbia, Ernest Ncha; Fabricius, Ida Lykke; Oji, C. O.

2011-01-01

interval 6 is mainly shale. X-ray diffraction analysis reveals the dominance of inter-layered smectite/illite in interval 1–3 and upper part of interval 4, whereas illite dominates interval 5 and 6. Other minerals include kaolinite, chlorite, quartz, calcite, Opal-CT, dolomite and plagioclase...

On the complex conductivity signatures of calcite precipitation

Energy Technology Data Exchange (ETDEWEB)

Wu, Yuxin; Hubbard, Susan; Williams, Kenneth Hurst; Ajo-Franklin, Jonathan

2009-11-01

Calcite is a mineral phase that frequently precipitates during subsurface remediation or geotechnical engineering processes. This precipitation can lead to changes in the overall behavior of the system, such as flow alternation and soil strengthening. Because induced calcite precipitation is typically quite variable in space and time, monitoring its distribution in the subsurface is a challenge. In this research, we conducted a laboratory column experiment to investigate the potential of complex conductivity as a mean to remotely monitor calcite precipitation. Calcite precipitation was induced in a glass bead (3 mm) packed column through abiotic mixing of CaCl{sub 2} and Na{sub 2}CO{sub 3} solutions. The experiment continued for 12 days with a constant precipitation rate of {approx}0.6 milimole/d. Visual observations and scanning electron microscopy imaging revealed two distinct phases of precipitation: an earlier phase dominated by well distributed, discrete precipitates and a later phase characterized by localized precipitate aggregation and associated pore clogging. Complex conductivity measurements exhibited polarization signals that were characteristic of both phases of calcite precipitation, with the precipitation volume and crystal size controlling the overall polarization magnitude and relaxation time constant. We attribute the observed responses to polarization at the electrical double layer surrounding calcite crystals. Our experiment illustrates the potential of electrical methods for characterizing the distribution and aggregation state of nonconductive minerals like calcite. Advancing our ability to quantify geochemical transformations using such noninvasive methods is expected to facilitate our understanding of complex processes associated with natural subsurface systems as well as processes induced through engineered treatments (such as environmental remediation and carbon sequestration).

Controls of Ca/Mg/Fe activity ratios in pore water chemistry models of the Callovian-Oxfordian clay formation

International Nuclear Information System (INIS)

Lerouge, C.; Grangeon, S.; Wille, G.; Flehoc, C.; Gailhanou, H.; Gaucher, E.C.; Tournassat, C.; Vinsot, A.; Made, B.; Altmann, S.

2013-01-01

In the pore water chemistry model of the Callovian-Oxfordian clay formation, the divalent cations Ca, Mg, and Fe are controlled by equilibrium reactions with pure carbonates: calcite for Ca, dolomite for Mg, and siderite for Fe. Results of a petrological study and computing of the Ca/Mg and Ca/Fe activity ratios based on natural pore water chemistry provide evidence that equilibrium with pure calcite and pure dolomite is a reasonable assumption for undisturbed pore waters; on the other hand, siderite cannot be considered at equilibrium with pore waters at the formation scale. (authors)

Controls of Ca/Mg/Fe activity ratios in pore water chemistry models of the Callovian-Oxfordian clay formation

Energy Technology Data Exchange (ETDEWEB)

Lerouge, C.; Grangeon, S.; Wille, G.; Flehoc, C.; Gailhanou, H.; Gaucher, E.C.; Tournassat, C. [BRGM av. Claude Guillemin BP6009 45060 Orleans cedex 2 (France); Vinsot, A. [ANDRA Meuse/Haute-Marne Underground research Laboratory (URL), RD 960, 55290 Bure (France); Made, B.; Altmann, S. [ANDRA - Parc de la Croix Blanche, 1-7 rue Jean Monnet, 92298 Chatenay-Malabry Cedex (France)

2013-07-01

In the pore water chemistry model of the Callovian-Oxfordian clay formation, the divalent cations Ca, Mg, and Fe are controlled by equilibrium reactions with pure carbonates: calcite for Ca, dolomite for Mg, and siderite for Fe. Results of a petrological study and computing of the Ca/Mg and Ca/Fe activity ratios based on natural pore water chemistry provide evidence that equilibrium with pure calcite and pure dolomite is a reasonable assumption for undisturbed pore waters; on the other hand, siderite cannot be considered at equilibrium with pore waters at the formation scale. (authors)

PVC mixtures’ mechanical properties with the addition of modified calcite as filler

Directory of Open Access Journals (Sweden)

Vučinić Dušica R.

2012-01-01

Full Text Available In this study mechanical properties of PVC mixtures (PVC, stabilizer, lubricant, filler such as tensile strength, tensile elongation, breaking strength, and breaking elongation were investigated. Unmodified calcite, as well as calcite modified by stearic acid, were used as fillers in wet and dry processes. The PVC mixtures containing the calcite modified by wet procedure have better mechanical properties compared to those with the calcite modified by the dry process. Tensile and breaking strength of the PVC mixture containing the calcite modified with 1.5% stearic acid using wet process, are higher for 2.8% and 5.2%, respectively, compared to the PVC mixture containing the calcite modified with the same amount of acid used in the dry process. The tensile strength difference between the mixtures increases with the increase of the concentration of used stearic acid up to 3%. The strength of PVC mixture with the calcite modified by wet process is 3.1% higher compared to the mixture containing calcite modified by dry process. The results showed that the bonding strength between calcite and the adsorbed organic component affected tensile strength, tensile elongation and breaking strength of the PVC mixtures. The best filler was obtained by wet modification using 1.5% stearic acid solution that provided the formation of a stearate monolayer chemisorbed on calcite. The PVC mixtures containing the calcite modified by wet process using 1.5% stearic acid solution exhibited the best mechanical properties. This calcite was completely hydrophobic with dominant chemically adsorbed surfactant, which means that stearate chemisorbed on calcite provided stronger interaction in the calcite-stearic acid-PVC system.

Geology of dolomite-hosted uranium deposits at the Pitch Mine, Saguache County, Colorado

International Nuclear Information System (INIS)

Nash, J.T.

1981-01-01

Newly documented uranium ore in the Pitch mine occurs chiefly in brecciated Mississippian Leadville Dolomite along the Chester upthrust zone, and to a lesser extent in sandstone, siltstone, and carbonaceous shale of the Pennsylvanian Belden Formation and in Precambrian granitic rocks and schist. Uranium-mineralized zones are generally thicker, more consistent, and of higher grade in dolomite than in other hosts, and roughly 50 percent of the new reserves are in dolomite. Strong physical control by dolomite is evident, as this is the only rock type that is pervasively brecciated within the fault slices that make up the footwall of the reverse-fault zone. Other rocks tended to either remain unbroken or undergo ductile deformation. Chemical controls on uranium deposition are subtle and appear chiefly to involve coprecipitation of FeS 2 as pyrite and marcasite, suggesting that sulfide ion may be the reductant

Calcite precipitates in Slovenian bottled waters.

Science.gov (United States)

Stanič, Tamara Ferjan; Miler, Miloš; Brenčič, Mihael; Gosar, Mateja

2017-06-01

Storage of bottled waters in varying ambient conditions affects its characteristics. Different storage conditions cause changes in the initial chemical composition of bottled water which lead to the occurrence of precipitates with various morphologies. In order to assess the relationship between water composition, storage conditions and precipitate morphology, a study of four brands of Slovenian bottled water stored in PET bottles was carried out. Chemical analyses of the main ions and measurements of the physical properties of water samples were performed before and after storage of water samples at different ambient conditions. SEM/EDS analysis of precipitates was performed after elapsed storage time. The results show that the presence of Mg 2+ , SO 4 2- , SiO 2 , Al, Mn and other impurities such as K + , Na + , Ba and Sr in the water controlled precipitate morphology by inhibiting crystal growth and leading to elongated rhombohedral calcite crystal forms which exhibit furrowed surfaces and calcite rosettes. Different storage conditions, however, affected the number of crystallization nuclei and size of calcite crystals. Hollow calcite spheres composed of cleavage rhombohedrons formed in the water with variable storage conditions by a combination of evaporation and precipitation of water droplets during high temperatures or by the bubble templating method.

Early diagenesis driven by widespread meteoric infiltration of a Central European carbonate ramp: A reinterpretation of the Upper Muschelkalk

Science.gov (United States)

Adams, Arthur; Diamond, Larryn W.

2017-12-01

Meteoric diagenesis of carbonate ramps is often difficult to interpret and can commonly be confused with other coinciding diagenetic processes. The Middle Triassic Upper Muschelkalk of Switzerland provides an insightful case in which the effects of several overprinting diagenetic environments, including matrix dolomitization, can be clearly unravelled. Previous studies suggested that diagenesis took place in connate marine waters, with later meteoric waters being invoked to explain recrystallization of dolomite. In this study, diagenetic analyses (C-O stable isotope ratios, thin-section point counting, cathodoluminescence and UV-fluorescence microscopy) of calcitic bioclastic samples have revealed that early diagenesis (pre-stylolitization) and the accompanying porosity evolution did not occur exclusively in the presence of marine fluids. Five sequential stages of diagenesis have been identified: marine, shallow burial, mixing-zone, meteoric and dolomitization. Marine diagenesis induced precipitation of bladed and inclusion-rich syntaxial cements that fluoresce strongly under UV-light. Both cements account for a mean 7.5 vol% reduction in the porosity of bioclastic beds. Shallow burial diagenesis likely induced mouldic porosity and associated fluorescent dog-tooth cementation. Based on light oxygen isotope and elevated strontium isotope ratios, matrix aragonite-calcite neomorphism is interpreted to have occurred in a mixture of marine and meteoric fluids. The combination of shallow burial and mixing-zone processes reduced porosity on average by 4.8 vol%. Evidence for subsequent meteoric diagenesis is found in abundant dog-tooth and blocky calcite cements that have mean δ18OVPDB of - 9.36‰ and no signs of recrystallization. These meteoric cements reduced porosity by a further 13.4 vol%. Percolation of meteoric water through the ramp was driven by hydraulic gradients on an adjacent basement high, which was exposed by a cycle of early Ladinian regressions

Role of Fungi in the Biomineralization of Calcite

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Saskia Bindschedler

2016-05-01

Full Text Available In the field of microbial biomineralization, much of the scientific attention is focused on processes carried out by prokaryotes, in particular bacteria, even though fungi are also known to be involved in biogeochemical cycles in numerous ways. They are traditionally recognized as key players in organic matter recycling, as nutrient suppliers via mineral weathering, as well as large producers of organic acids such as oxalic acid for instance, an activity leading to the genesis of various metal complexes such as metal-oxalate. Their implications in the transformation of various mineral and metallic compounds has been widely acknowledged during the last decade, however, currently, their contribution to the genesis of a common biomineral, calcite, needs to be more thoroughly documented. Calcite is observed in many ecosystems and plays an essential role in the biogeochemical cycles of both carbon (C and calcium (Ca. It may be physicochemical or biogenic in origin and numerous organisms have been recognized to control or induce its biomineralization. While fungi have often been suspected of being involved in this process in terrestrial environments, only scarce information supports this hypothesis in natural settings. As a result, calcite biomineralization by microbes is still largely attributed to bacteria at present. However, in some terrestrial environments there are particular calcitic habits that have been described as being fungal in origin. In addition to this, several studies dealing with axenic cultures of fungi have demonstrated the ability of fungi to produce calcite. Examples of fungal biomineralization range from induced to organomineralization processes. More examples of calcite biomineralization related to direct fungal activity, or at least to their presence, have been described within the last decade. However, the peculiar mechanisms leading to calcite biomineralization by fungi remain incompletely understood and more research is

Surface Forces Apparatus measurements of interactions between rough and reactive calcite surfaces.

Science.gov (United States)

Dziadkowiec, Joanna; Javadi, Shaghayegh; Bratvold, Jon Einar; Nilsen, Ola; Røyne, Anja

2018-05-28

Nm-range forces acting between calcite surfaces in water affect macroscopic properties of carbonate rocks and calcite-based granular materials, and are significantly influenced by calcite surface recrystallization. We suggest that the repulsive mechanical effects related to nm-scale surface recrystallization of calcite in water could be partially responsible for the observed decrease of cohesion in calcitic rocks saturated with water. Using the Surface Forces Apparatus (SFA), we simultaneously followed the calcite reactivity and measured the forces in water in two surface configurations: between two rough calcite surfaces (CC), or between rough calcite and a smooth mica surface (CM). We used nm-scale rough, polycrystalline calcite films prepared by Atomic Layer Deposition (ALD). We measured only repulsive forces in CC in CaCO 3 -saturated water, which was related to roughness and possibly to repulsive hydration effects. Adhesive or repulsive forces were measured in CM in CaCO 3 -saturated water depending on calcite roughness, and the adhesion was likely enhanced by electrostatic effects. The pull-off adhesive force in CM became stronger with time and this increase was correlated with a decrease of roughness at contacts, which parameter could be estimated from the measured force-distance curves. That suggested a progressive increase of real contact areas between the surfaces, caused by gradual pressure-driven deformation of calcite surface asperities during repeated loading-unloading cycles. Reactivity of calcite was affected by mass transport across nm to µm-thick gaps between the surfaces. Major roughening was observed only for the smoothest calcite films, where gaps between two opposing surfaces were nm-thick over µm-sized areas, and led to force of crystallization that could overcome confining pressures of the order of MPa. Any substantial roughening of calcite caused a significant increase of the repulsive mechanical force contribution.

Molecular ordering of ethanol at the calcite surface

DEFF Research Database (Denmark)

Pasarín, I. S.; Yang, M.; Bovet, Nicolas Emile

2012-01-01

To produce biominerals, such as shells, bones, and teeth, living beings create organic compounds that control the growth of the solid phase. Investigating the atomic scale behavior of individual functional groups at the mineral-fluid interface provides fundamental information that is useful...... for constructing accurate predictive models for natural systems. Previous investigations of the activity of coccolith-associated polysaccharides (CAP) on calcite, using atomic force microscopy (AFM) [ Henriksen, K., Young, J. R., Bown, P. R., and Stipp, S. L. S.Palentology 2004, 43 (Part 3), 725...... dynamics (MD) simulations, the structuring on calcite of a layer of the simplest carbon chain molecule that contains an OH group, ethanol (CH 3-CH2-OH). We found evidence that EtOH forms a highly ordered structure at the calcite surface, where the first layer molecules bond with calcite. The ethanol...

Paleotransport of lanthanides and strontium recorded in calcite compositions from tuffs at Yucca Mountain, Nevada, USA

International Nuclear Information System (INIS)

Vaniman, D.T.; Chipera, S.J.

1996-01-01

Secondary calcite occurs in both saturated and unsaturated hydrologic zones (SZ and UZ, respectively) in the tuffs at Yucca Mountain, Nevada, USA. In the upper UZ, the major constituents of the calcite crystal structure (C, O) have surface origins. At greater depth there is a open-quotes barren zone,close quotes straddling the water table, where calcite is rare and mixing of surface and subsurface sources may occur. Deep in the SZ, distinctive Mn calcites reflect deep sources, including Ca released as analcime or albite formed and carbonates derived from underlying Paleozoic rocks. In the UZ and in the barren zone, above the deep Mn calcites, variations in calcite lanthanide chemistry can be used to distinguish rhyolitic from quartz-latitic sources. Lanthanide ratios and Sr contents of calcites record the chemical evolution of waters flowing through the UZ and upper SZ. Variations in calcite chemistry in the UZ and in the barren zone show that (1) Sr, which is readily exchanged with clays or zeolites, is essentially removed from some flowpaths that are in contact with these minerals and (2) traces of Mn oxides found in the tuffs have a significant effect of groundwater chemistry in the UZ and in the barren zone by removing almost all Ce from solution (evidenced by characteristic Ce depletions in calcite throughout this zone). Extreme Ce removal may be a result of Ce oxidation (Ce 3+ → Ce 4+ ) at the surfaces of some Mn oxides, particularly rancieite. Higher Sr contents and lack of Ce depletions in the deeper Mn calcites reflect different ages, origins, and transport systems. The calcite record of lanthanide and Sr transport in the UZ shows that minor minerals (clays and zeolites) and even trace minerals (Mn oxides) will affect the compositions of groundwaters that flow over distances greater than a few tens of meters. 43 refs., 8 figs., 4 tabs

Geobacillus thermoglucosidasius Endospores Function as Nuclei for the Formation of Single Calcite Crystals

Science.gov (United States)

Murai, Rie

2013-01-01

Geobacillus thermoglucosidasius colonies were placed on an agar hydrogel containing acetate, calcium ions, and magnesium ions, resulting in the formation of single calcite crystals (calcites) within and peripheral to the plating area or parent colony. Microscopic observation of purified calcites placed on the surface of soybean casein digest (SCD) nutrient medium revealed interior crevices from which bacterial colonies originated. Calcites formed on the gel contained [1-13C]- and [2-13C]acetate, demonstrating that G. thermoglucosidasius utilizes carbon derived from acetate for calcite formation. During calcite formation, vegetative cells swam away from the parent colony in the hydrogel. Hard-agar hydrogel inhibited the formation of calcites peripheral to the parent colony. The calcite dissolved completely in 1 M HCl, with production of bubbles, and the remaining endospore-like particles were easily stained with Brilliant green dye. The presence of DNA and protein in calcites was demonstrated by electrophoresis. We propose that endospores initiate the nucleation of calcites. Endospores of G. thermoglucosidasius remain alive and encapsulated in calcites. PMID:23455343

Acidization of shales with calcite cemented fractures

Science.gov (United States)

Kwiatkowski, Kamil; Szymczak, Piotr; Jarosiński, Marek

2017-04-01

Investigation of cores drilled from shale formations reveals a relatively large number of calcite-cemented fractures. Usually such fractures are reactivated during fracking and can contribute considerably to the permeability of the resulting fracture network. However, calcite coating on their surfaces effectively excludes them from production. Dissolution of the calcite cement by acidic fluids is investigated numerically with focus on the evolution of fracture morphology. Available surface area, breakthrough time, and reactant penetration length are calculated. Natural fractures in cores from Pomeranian shale formation (northern Poland) were analyzed and classified. Representative fractures are relatively thin (0.1 mm), flat and completely sealed with calcite. Next, the morphology evolution of reactivated natural fractures treated with low-pH fluids has been simulated numerically under various operating conditions. Depth-averaged equations for fracture flow and reactant transport has been solved by finite-difference method coupled with sparse-matrix solver. Transport-limited dissolution has been considered, which corresponds to the treatment with strong acids, such as HCl. Calcite coating in reactivated natural fractures dissolves in a highly non-homogeneous manner - a positive feedback between fluid transport and calcite dissolution leads to the spontaneous formation of wormhole-like patterns, in which most of the flow is focused. The wormholes carry reactive fluids deeper inside the system, which dramatically increases the range of the treatment. Non-uniformity of the dissolution patterns provides a way of retaining the fracture permeability even in the absence of the proppant, since the less dissolved regions will act as supports to keep more dissolved regions open. Evolution of fracture morphology is shown to depend strongly on the thickness of calcite layer - the thicker the coating the more pronounced wormholes are observed. However the interaction between

EPR and X-ray diffraction investigation of some Greek marbles and limestones

International Nuclear Information System (INIS)

Duliu, Octavian; Grecu, Maria Nicoleta; Cristea, Corina

2009-01-01

Twelve different marble and limestone samples collected from well-known Greek quarries have been investigated by X-ray diffraction and electron paramagnetic resonance (EPR). X-ray diffraction spectra permitted to determine both major (calcite and dolomite) and minor (quartz or magnesite) mineralogical components. EPR has been used to investigate the same samples unirradiated and after 10 kGy gamma-ray irradiation. The unirradiated samples display typical EPR spectra of Mn 2+ in calcite and dolomite as well as a superposition of these while some samples displayed EPR free radicals signals of centers (low field signal) and centers (high field signal). From X-ray diffraction and EPR spectra it was possible to extract numerical values of several numerical parameters such as dolomite to calcite ratio, EPR intensity parameter, and low field to high field EPR signals intensity ratio. These values as well as the correlation coefficients between the digital functions that described the low field Mn 2+ ions EPR line have been used as entry data for cluster analysis to quantify the resemblance and differences between analyzed samples. (authors)

Biocementation of Concrete Pavements Using Microbially Induced Calcite Precipitation.

Science.gov (United States)

Jeong, Jin-Hoon; Jo, Yoon-Soo; Park, Chang-Seon; Kang, Chang-Ho; So, Jae-Seong

2017-07-28

In this study, the feasibility of introducing calcite-forming bacteria into concrete pavements to improve their mechanical performance was investigated. Lysinibacillus sphaericus WJ-8, which was isolated in a previous study and is capable of exhibiting high urease activity and calcite production, was used. When analyzed via scanning electron microscopy (SEM) and X-ray diffraction, WJ-8 showed a significant amount of calcite precipitation. The compressive strength of cement mortar mixed with WJ-8 cells and nutrient medium (urea with calcium lactate) increased by 10% compared with that of the controls. Energy dispersive x-ray spectroscopy analyses confirmed that the increase in strength was due to the calcite formed by the WJ-8 cells.

Uranyl incorporation into calcite and aragonite: XAFS and luminescence studies

International Nuclear Information System (INIS)

Reeder, R.J.; Nugent, M.; Lamble, G.M.; Tait, C.D.; Morris, D.E.

2000-01-01

X-ray absorption, luminescence, and Raman spectroscopic studies of U(VI)-containing calcite and aragonite show that the UO 2 2+ ion, the dominant and mobile form of dissolved uranium in near-surface waters, has a disordered and apparently less stable coordination environment when incorporated into calcite in comparison to aragonite, both common polymorphs of CaCO 3 . Their findings suggest that calcite, a widely distributed authigenic mineral in soils and near-surface sediments and a principal weathering product of concrete-based containment structures, is not likely to be a suitable host for the long-term sequestration of U(VI). The more stable coordination provided by aragonite suggests that its long-term retention should be favored in this phase, until it inverts to calcite. Consequently, future remobilization of U(VI) coprecipitated with calcium carbonate minerals should not be ruled out in assessments of contaminated sites. Their observation of a similar equatorial coordination of UO 2 2+ in aragonite and the dominant aqueous species [UO 2 (CO 3 ) 3 4- ] but a different coordination in calcite indicates that a change in UO 2 2+ coordination is required for its incorporation into calcite. This may explain the observed preferential uptake of U(VI) by aragonite relative to calcite

Ecological indices of manufacture of Portland cement clinker and production of the dolomite clinker

Directory of Open Access Journals (Sweden)

Vinnichenko Varvara

2017-01-01

Full Text Available It is shown that the production of dolomite clinker in comparison with that of Portland cement is environmentally appropriate. When calcining dolomite for cementitious binder, the pollution of the atmosphere by carbon dioxide is reduced due to its isolation during decarbonization reactions of calcium carbonates. Reducing fuel consumption for clinker burning provides less carbon dioxide emissions from combustion products. Reducing the firing temperature creates obstacles to the formation of nitrogen oxides. The production of binders from dolomite in comparison with the production of Portland cement helps to protect the environment from contamination

Characterization of Qatar's surface carbonates for CO2 capture and thermochemical energy storage

Science.gov (United States)

Kakosimos, Konstantinos E.; Al-Haddad, Ghadeer; Sakellariou, Kyriaki G.; Pagkoura, Chrysa; Konstandopoulos, Athanasios G.

2017-06-01

Samples of surface carbonates were collected from three different areas of the Qatar peninsula. We employed material characterization techniques to examine the morphology and composition of the samples, while their CO2 capture capacity was assessed via multiple successive calcination-carbonation cycles. Our samples were mainly calcite and dolomite based. Calcite samples showed higher initial capacity of around 11 mmol CO2 g-1 which decayed rapidly to less than 2 mmol CO2 g-1. On the other hand, dolomite samples showed an excellent stability (˜15 cycles) with a capacity of 6 mmol CO2 g-1. The performance of the dolomite samples is better compared to other similar natural samples, from literature. A promising result for future studies towards improving their performance by physical and chemical modification.

Structural incorporation of Neptunyl(V) into Calcite: Interfacial Reactions and Kinetics

OpenAIRE

Heberling, Frank

2010-01-01

In this experimental work the calcite-water interface is characterized by means of zetapotential and surface diffraction measurements. Based on the experimental results a new Basic Stern Surface Complexation model for calcite is developed. Neptunyl(V) adsorption at the calcite surface and incorporation into the calcite structure is studied by batch type adsorption- and mixed flow reactor experiments. Adsorption and incorporation species of Neptunyl are investigated by EXAFS spectroscopy.

Modelization of reactive transport: application to the dedolomitization (Institut del Ciencies de la Tierr, CSIC, Barcelona (ES))

International Nuclear Information System (INIS)

Ayora, C.; Taberner, C.; Samper, J.

1994-01-01

The replacement of dolomite with calcite (dedolomization) has been analyzed by means of two numerical models of reactive transport. The results of successive calculations under different scenarios have been compared with the observations made on the dedolomites developed on the Triassic strata from Prades (Tarragona, Spain). The model based on the local equilibrium assumption for water-rock interaction does not predict the development of the porosity associated to the replacement. The model based on kinetic laws for mineral dissolution and precipitation does predict the observed proportions of calcite, dolomite and porosity. The result of modeling under kinetic laws is sensitive to parameters such as the flow velocity, the chemical composition of the recharge water and the reactive surface of the minerals. The replacement and associated porosity is only formed for infiltration flows higher than 100 mm/year. The water has a neutral to slightly alkaline pH, far from equilibrium with carbonates and the atmosphere. The calcium concentrations must be one order of magnitude higher the average of surficial waters, probably due to sulfate dissolution. The reactive surface of dolomite has been estimated from a simple geometric model of fractures, whereas that of calcite has been inferred from calculations based on nucleation and crystal growth theory. The reactive surface of calcite appears to be several orders of magnitude lower than that of dolomite, in agreement with what is required for reactive transport calculations to generate porosity. The dedolomization and associated porosity takes place in the first meter of aquifers, whereas downstream the replacement vanishes and does not create porosity

High resolution cathodoluminescence spectroscopy of carbonate cementation in Khurmala Formation (Paleocene-L. Eocene) from Iraqi Kurdistan Region, Northern Iraq

Science.gov (United States)

Omer, Muhamed F.; Omer, Dilshad; Zebari, Bahroz Gh.

2014-12-01

A combination of high resolution cathodoluminsecnce-spectroscopy (HRS-CL) with spatial electron microprobe analysis and optical microscopy is used to determine paragenesis and history of cementation in the limestones and dolostones of Khurmala Formation which is exposed in many parts of Northern Iraq. Khurmala Formation was subjected to different diagenetic processes such as micritization, compaction, dissolution, neomorphism, pyritization and cementation that occurred during marine to shallow burial stages and culminated during intermediate to deep burial later stages. Five dolomite textures are recognized and classified according to crystal size distribution and crystal-boundary shape. Dolomitization is closely associated with the development of secondary porosity that pre-and postdates dissolution and corrosion; meanwhile such porosity was not noticed in the associated limestones. Microprobe analysis revealed three types of cement, calcite, dolomite and ankerite which range in their luminescence from dull to bright. Cathodoluminescence study indicated four main texture generations. These are (1) unzoned microdolomite of planar and subhedral shape, with syntaxial rim cement of echinoderm that show dull to red luminescence, (2) equant calcite cements filling interparticle pores which shows dull luminescence and weak zonal growth, (3.1) homogenous intrinsic blue stoichiometric calcite with dull luminescence and without activators, (3.2) coarse blocky calcite cement with strong oscillatory zoning and bright orange luminescence which postdates other calcite cements, (4) ankerite cement with red to orange, non-luminescence growth zonation which is the last formed cement.

The coordination of sulfur in synthetic and biogenic Mg calcites: The red coral case

Science.gov (United States)

Perrin, J.; Rivard, C.; Vielzeuf, D.; Laporte, D.; Fonquernie, C.; Ricolleau, A.; Cotte, M.; Floquet, N.

2017-01-01

Sulfur has been recognized in biogenic calcites for a long time. However, its structural position is matter of debate. For some authors, sulfur is a marker of the organic matrix while it is part of the calcite structure itself for others. To better understand the place of sulfur in calcite, sulfated magnesian calcites (S-MgCalcite) have been synthetized at high pressure and temperature and studied by μ-XANES spectroscopy. S-MgCalcite XANES spectra show two different types of sulfur: sulfate (SO42-) as a predominant species and a small contribution of sulfite (SO32-), both substituting for carbonate ions in the calcite structure. To address the question of the position of sulfur in biogenic calcites, the oxidation states of sulfur in the skeleton and organic tissues of Corallium rubrum have been investigated by micro X-ray fluorescence (μ-XRF) and sulfur K-edge micro X-ray absorption near edge structure (μ-XANES) spectroscopy at the European Synchrotron Radiation Facility (ESRF, Grenoble, France) on beamline ID21. In the skeleton, sulfur is mainly present as oxidized sulfur SO42- (+VI), plus a weak sulfite contribution. XANES spectra indicate that sulfur is inorganically incorporated as sulfur structurally substituted to carbonate ions (SSS). Although an organic matrix is present in the red coral skeleton, reduced organic sulfur could not be detected by μ-XANES spectroscopy in the skeleton probably due to low organic/inorganic sulfur ratio. In the organic tissues surrounding the skeleton, several sulfur oxidation states have been detected including disulfide (S-S), thioether (R-S-CH3), sulfoxide (SO2), sulfonate (SO2O-) and sulfate (SO42-). The unexpected occurrence of inorganic sulfate within the organic tissues suggests the presence of pre-organized organic/inorganic complexes in the circulatory system of the red coral, precursors to biomineralization ahead of the growth front.

Cretaceous joints in southeastern Canada: dating calcite-filled fractures

Science.gov (United States)

Schneider, David; Spalding, Jennifer; Gautheron, Cécile; Sarda, Philippe; Davis, Donald; Petts, Duane

2017-04-01

To resolve the timing of brittle tectonism is a challenge since the classical chronometers required for analyses are not often in equilibrium with the surrounding material or simply absent. In this study, we propose to couple LA-ICP-MS U-Pb and (U-Th)/He dating with geochemical proxies in vein calcite to tackle this dilemma. We examined intracratonic Middle Ordovician limestone bedrock that overlies Mesoproterozoic crystalline basement, which are cut by NE-trending fault zones that have historic M4-5 earthquakes along their trace. E-W to NE-SW vertical joint sets, the relatively youngest stress recorded in the bedrock, possess 1-7 mm thick calcite veins that seal fractures or coat fracture surfaces. The veins possess intragranular calcite that are lined with fine-grained calcite along the vein margin and can exhibit µm- to mm-scale offset (e.g. displaced fossil fragments in host rock). Calcite d18O and d13C values are analogous to the bulk composition of Middle to Late Ordovician limestones, and suggest vein formation from a source dominated by connate fluids. The calcite contain trails of fluid inclusions commonly along fractures, and 3He/4He analyses indicate a primitive, deep fluid signature (R/Ra: 0.5-2.7). Trace element geochemistry of the calcite is highly variable, generally following the elevated HREE and lower LREE of continental crust trends but individual crystals from a single vein may vary by three orders of magnitude. LA-ICP-MS geochemical traverse across veins show elevated concentrations along (sub)grain boundaries and the vein-host rock contact. Despite abundant helium concentrations, (U-Th)/He dating was unsuccessful yielding highly dispersed dates likely from excess helium derived from the fluid inclusions. However, LA-ICP-MS U-Pb dating on calcite separated from the veins yielded model ages of 110.7 ± 6.8 Ma (MSWD: 0.53; n: 16) to 81.4 ± 8.3 Ma (MSWD: 2.6; n: 17). Since all veins are from the same ENE-trend, we regressed all the calcite dates

Effects of dicyandiamide and dolomite application on N2O emission from an acidic soil.

Science.gov (United States)

Shaaban, Muhammad; Wu, Yupeng; Peng, Qi-an; Lin, Shan; Mo, Yongliang; Wu, Lei; Hu, Ronggui; Zhou, Wei

2016-04-01

Soil acidification is a major problem for sustainable agriculture since it limits productivity of several crops. Liming is usually adopted to ameliorate soil acidity that can trigger soil processes such as nitrification, denitrification, and loss of nitrogen (N) as nitrous oxide (N2O) emissions. The loss of N following liming of acidic soils can be controlled by nitrification inhibitors (such as dicyandiamide). However, effects of nitrification inhibitors following liming of acidic soils are not well understood so far. Here, we conducted a laboratory study using an acidic soil to examine the effects of dolomite and dicyandiamide (DCD) application on N2O emissions. Three levels of DCD (0, 10, and 20 mg kg(-1); DCD0, DCD10, and DCD20, respectively) were applied to the acidic soil under two levels of dolomite (0 and 1 g kg(-1)) which were further treated with two levels of N fertilizer (0 and 200 mg N kg(-1)). Results showed that N2O emissions were highest at low soil pH levels in fertilizer-treated soil without application of DCD and dolomite. Application of DCD and dolomite significantly (P ≤ 0.001) reduced N2O emissions through decreasing rates of NH4 (+)-N oxidation and increasing soil pH, respectively. Total N2O emissions were reduced by 44 and 13% in DCD20 and dolomite alone treatments, respectively, while DCD20 + dolomite reduced N2O emissions by 54% when compared with DCD0 treatment. The present study suggests that application of DCD and dolomite to acidic soils can mitigate N2O emissions.

Influence of ameliorating soil acidity with dolomite on the priming of soil C content and CO2 emission.

Science.gov (United States)

Shaaban, Muhammad; Wu, Lei; Peng, Qi-An; van Zwieten, Lukas; Chhajro, Muhammad Afzal; Wu, Yupeng; Lin, Shan; Ahmed, Muhammad Mahmood; Khalid, Muhammad Salman; Abid, Muhammad; Hu, Ronggui

2017-04-01

Lime or dolomite is commonly implemented to ameliorate soil acidity. However, the impact of dolomite on CO 2 emissions from acidic soils is largely unknown. A 53-day laboratory study was carried out to investigate CO 2 emissions by applying dolomite to an acidic Acrisol (rice-rapeseed rotation [RR soil]) and a Ferralsol (rice-fallow/flooded rotation [RF soil]). Dolomite was dosed at 0, 0.5, and 1.5 g 100 g -1 soil, herein referred to as CK, L, and H, respectively. The soil pH (H2O) increased from 5.25 to 7.03 and 7.62 in L and H treatments of the RR soil and from 5.52 to 7.27 and 7.77 in L and H treatments of the RF soil, respectively. Dolomite application significantly (p ≤ 0.001) increased CO 2 emissions in both RR and RF soils, with higher emissions in H as compared to L dose of dolomite. The cumulative CO 2 emissions with H dose of dolomite were greater 136% in the RR soil and 149% in the RF soil as compared to CK, respectively. Dissolved organic carbon (DOC) and microbial biomass carbon (MBC) increased and reached at 193 and 431 mg kg -1 in the RR soil and 244 and 481 mg kg -1 in the RF soil by H treatments. The NH 4 - -N and NO 3 - -N were also increased by dolomite application. The increase in C and N contents stimulated microbial activities and therefore higher respiration in dolomite-treated soil as compared to untreated. The results suggest that CO 2 release in dolomite-treated soils was due to the priming of soil C content rather than chemical reactions.

Examination of TL and optical absorption in calcite's mineral

International Nuclear Information System (INIS)

Sabikoglu, I.; Can, N.

2009-01-01

Calcite which is a form of crystalline of the calcium carbonate composes parent material of chalk stone (limestone) and marble. Calcite which presents in various colors also in our country consists of yellow, blue, transparent and green colors. In this study, green calcite mineral which is taken from the region of Ayvalik, was examined of its thermoluminescence (TL) and optical absorption features in different doses. It has been obtained a large TL peak in 179 degree C and absorption peak in 550 mm.

Calcite Wettability in the Presence of Dissolved Mg2+ and SO42-

DEFF Research Database (Denmark)

Generosi, Johanna; Ceccato, Marcel; Andersson, Martin Peter

2017-01-01

that potential determining ions in seawater, Mg2+, Ca2+, and SO42–, are responsible for altering the wettability of calcite surfaces. In favorable conditions, e.g., elevated temperature, calcium at the calcite surface can be replaced by magnesium, making organic molecules bind more weakly and water molecules...... bind more strongly, rendering the surface more hydrophilic. We used atomic force microscopy in chemical force mapping mode to probe the adhesion forces between a hydrophobic CH3-terminated AFM tip and a freshly cleaved calcite {10.4} surface to investigate wettability change in the presence of Mg2...... with calcite even after rinsing with CaCO3-saturated deionized water, suggesting sorption on or in calcite. When the calcite-saturated solution of MgSO4 was replaced by calcite-saturated NaCl at the same ionic strength, adhesion force increased again, indicating that the effect is reversible and suggesting Mg...

Calcite biomineralization in coccoliths: Evidence from atomic force microscopy (AFM)

DEFF Research Database (Denmark)

Henriksen, Karen; Stipp, S.L.S.

2002-01-01

geochemistry, crystal orientation, coccolith function, biomineralization, biological calcite, atomic force microscopy......geochemistry, crystal orientation, coccolith function, biomineralization, biological calcite, atomic force microscopy...

Substrate pH and butterfly bush response to dolomitic lime or steel slag amendment

Science.gov (United States)

Steel slag is a fertilizer amendment with a high concentration of calcium oxide, and thus capable of raising substrate pH similar to dolomitic lime. Steel slag, however, contains higher concentrations of some nutrients, such as iron, manganese, and silicon, compared to dolomitic lime. The objectiv...

Review of aragonite and calcite crystal morphogenesis in thermal spring systems

Science.gov (United States)

Jones, Brian

2017-06-01

Aragonite and calcite crystals are the fundamental building blocks of calcareous thermal spring deposits. The diverse array of crystal morphologies found in these deposits, which includes monocrystals, mesocrystals, skeletal crystals, dendrites, and spherulites, are commonly precipitated under far-from-equilibrium conditions. Such crystals form through both abiotic and biotic processes. Many crystals develop through non-classical crystal growth models that involve the arrangement of nanocrystals in a precisely controlled crystallographic register. Calcite crystal morphogenesis has commonly been linked to a ;driving force;, which is a conceptual measure of the distance of the growth conditions from equilibrium conditions. Essentially, this scheme indicates that increasing levels of supersaturation and various other parameters that produce a progressive change from monocrystals and mesocrystals to skeletal crystals to crystallographic and non-crystallographic dendrites, to dumbbells, to spherulites. Despite the vast amount of information available from laboratory experiments and natural spring systems, the precise factors that control the driving force are open to debate. The fact that calcite crystal morphogenesis is still poorly understood is largely a reflection of the complexity of the factors that influence aragonite and calcite precipitation. Available information indicates that variations in calcite crystal morphogenesis can be attributed to physical and chemical parameters of the parent water, the presence of impurities, the addition of organic or inorganic additives to the water, the rate of crystal growth, and/or the presence of microbes and their associated biofilms. The problems in trying to relate crystal morphogenesis to specific environmental parameters arise because it is generally impossible to disentangle the controlling factor(s) from the vast array of potential parameters that may act alone or in unison with each other.

Biotic control of skeletal growth by scleractinian corals in aragonite-calcite seas.

Directory of Open Access Journals (Sweden)

Tomihiko Higuchi

Full Text Available Modern scleractinian coral skeletons are commonly composed of aragonite, the orthorhombic form of CaCO3. Under certain conditions, modern corals produce calcite as a secondary precipitate to fill pore space. However, coral construction of primary skeletons from calcite has yet to be demonstrated. We report a calcitic primary skeleton produced by the modern scleractinian coral Acropora tenuis. When uncalcified juveniles were incubated from the larval stage in seawater with low mMg/Ca levels, the juveniles constructed calcitic crystals in parts of the primary skeleton such as the septa; the deposits were observable under Raman microscopy. Using scanning electron microscopy, we observed different crystal morphologies of aragonite and calcite in a single juvenile skeleton. Quantitative analysis using X-ray diffraction showed that the majority of the skeleton was composed of aragonite even though we had exposed the juveniles to manipulated seawater before their initial crystal nucleation and growth processes. Our results indicate that the modern scleractinian coral Acropora mainly produces aragonite skeletons in both aragonite and calcite seas, but also has the ability to use calcite for part of its skeletal growth when incubated in calcite seas.

Thermal decomposition of natural dolomite

Indian Academy of Sciences (India)

TECS

calcite reported by Garcia Calvo et al (1990) indicates that the presence of impurities is a cause of variation of kinetic parameters obtained. The impurities could func- tion as catalysts owing to their influence in the crystalline structure. 3.3 X-ray diffraction analysis. Figure 2 depicts the powder X-ray diffraction pattern of.

Dissolution Kinetics of Icel-Aydincik Dolomite in Hydrochloric Acid

African Journals Online (AJOL)

NJD

Department of Mining Engineering, Faculty of Engineering and Architecture, Cukurova University, Balcali, ... 65 °C. It was observed that heterogeneous chemical reactions ..... Dolomite, Ph.D. thesis, Cukurova University, Adana, Turkey, 2004.

A new microenvironment for the formation of clay minerals: the example of authigenic halloysite-7Å and gibbsite in a stalactite from Agios Georgios Cave, Kilkis, north Greece

Directory of Open Access Journals (Sweden)

Elena Ifandi, University of Patras

2015-09-01

Full Text Available An unusual authigenic origin for halloysite and gibbsite is reported in a stalactite from Agios Georgios Cave, Kilkis. This speleothem includes mostly pure calcite whereas minor areas of Mg-rich calcite and scarce dolomite are present in four growth phases. Abundant pores are created due to imperfect coalescence of the calcite crystals. Several of them contain detrital muscovite, which was presumably transferred from the dripping water, during the formation of speleothem and has been variably altered to halloysite. Several pores in the stalactite contain different mineral assemblages that we interpret as in situ: halloysite-7Å, halloysite + silica, gibbsite + silica and gibbsite. The breakdown of the muscovite and the formation of halloysite require acidic conditions, which we suggest to have been established by potassium solubilising microorganisms. The silica minerals include spheroidal assemblages or needle-like and blade-like quartz and can be explained by further dissolution of halloysite, under the same acidic conditions in the presence of microorganisms. In our model, the precipitation of gibbsite is the result of direct formation from muscovite, promoted from abundant and undisturbed water percolation, at moderately low pH, also induced by the presence of bacteria. Given that microbial activities promote: (1 breakdown of muscovite and formation of halloysite, silica, and gibbsite, and (2 formation of Mg-calcite and dolomite after calcite, then it is likely that two or more different microbial communities may exist in the same speleothem. The first creates mild acidic conditions, aiming at the decomposition of muscovite in the microenvironment of the pores antagonising the second that produces alkaline microregimes and the local precipitation of Mg-rich carbonate minerals.

Influence of surface conductivity on the apparent zeta potential of calcite.

Science.gov (United States)

Li, Shuai; Leroy, Philippe; Heberling, Frank; Devau, Nicolas; Jougnot, Damien; Chiaberge, Christophe

2016-04-15

Zeta potential is a physicochemical parameter of particular importance in describing the surface electrical properties of charged porous media. However, the zeta potential of calcite is still poorly known because of the difficulty to interpret streaming potential experiments. The Helmholtz-Smoluchowski (HS) equation is widely used to estimate the apparent zeta potential from these experiments. However, this equation neglects the influence of surface conductivity on streaming potential. We present streaming potential and electrical conductivity measurements on a calcite powder in contact with an aqueous NaCl electrolyte. Our streaming potential model corrects the apparent zeta potential of calcite by accounting for the influence of surface conductivity and flow regime. We show that the HS equation seriously underestimates the zeta potential of calcite, particularly when the electrolyte is diluted (ionic strength ⩽ 0.01 M) because of calcite surface conductivity. The basic Stern model successfully predicted the corrected zeta potential by assuming that the zeta potential is located at the outer Helmholtz plane, i.e. without considering a stagnant diffuse layer at the calcite-water interface. The surface conductivity of calcite crystals was inferred from electrical conductivity measurements and computed using our basic Stern model. Surface conductivity was also successfully predicted by our surface complexation model. Copyright © 2016 Elsevier Inc. All rights reserved.

Transport of barium through dolomite rocks under the presence of guar gum and brine salinities of hydraulic fracturing wastewater

Science.gov (United States)

Ebrahimi, P.; Vilcaez, J.

2017-12-01

Hydraulic fracturing wastewater (HFW) containing high concentrations of Ba, is commonly disposed into the deep saline aquifers. We investigate the effect of brine salinity, competing cations (Ca and Mg), and guar gum (most common fracturing viscosifier) on the sorption and transport of Ba through dolomite rocks. To this aim, we have conducted batch sorption and core-flooding experiments at both ambient (22°C) and deep subsurface (60°C) temperature conditions. The effect of mineral composition is assessed by comparing batch and core-flooding experimental results obtained with sandstone and dolomite rocks. Batch sorption experiments conducted using powdered dolomite rocks (500-600 µm particle size) revealed that Ba sorption on dolomite greatly decreases with increasing brine salinity (0 - 180,000 mg-NaCl/L), and that at brine salinities of HFW, chloro-complexation reactions between Ba and Cl ions and changes in pH (that results from dolomite dissolution) are the controlling factors of Ba sorption on dolomite. Organo-complexation reactions between Ba and guar gum, and competition of Ba with common cations (Ca and Mg) for hydration sites of dolomite, play a secondary role. This finding is in accordance with core-flooding experimental results, showing that the transport of Ba through synthetic dolomite rocks of high flow properties (25-29.6% porosity, 9.6-13.7 mD permeability), increases with increasing brine salinity (0-180,000 mg-NaCl/L), while the presence of guar gum (50-500 mg/L) does not affect the transport of Ba. On the other hand, core-flooding experiments conducted using natural dolomite core plugs (6.5-8.6% porosity, 0.06-0.3 mD permeability), indicates that guar gum can clog the pore throats of tight dolomite rocks retarding the transport of Ba. Results of our numerical simulation studies indicate that the mechanism of Ba sorption on dolomite can be represented by a sorption model that accounts for both surface complexation reactions on three distinct

Magnesium production from Asian Abe-Gram dolomite in pidgeon-type reactor

International Nuclear Information System (INIS)

Mehrabi, B.; Abdellatifi, M.; Masoudi, F.

2011-01-01

Ore mineral characterization and various experimental test work were carried out on Asian Abe-Garm dolomite, Qazvin province, Iran. The test work consisted of calcining, chemical characterization, LOI determination, and reduction tests on the calcined dolomite (doloma), using Semnan ferrosilicon. Calcining of dolomite sample was carried out at about 1400 d egree C in order to remove the contained CO 2 , moisture, and other easily volatilised impurities. The doloma was milled, thoroughly mixed with 21 p ercent S emnan ferrosilicon and briquetted in hand press applying 30 MPa pressure. The briquettes were heated at 1125-1150 d egree C and 500 Pa in a Pidgeon-type tube reactor for 10-12 hours to extract the magnesium. Ferrosilicon addition, relative to doloma, was determined based on the chemical analysis of the two reactants using Mintek's Pyrosim software package. Magnesium extraction calculated as 77.97 p ercent a nd Mg purity of 96.35 p ercent . The level of major impurities in the produced magnesium crown is similar to those in the crude metal production.

Sorption and desorption of arsenate and arsenite on calcite

DEFF Research Database (Denmark)

Sø, Helle Ugilt; Postma, Diederik Jan; Jakobsen, Rasmus

2008-01-01

The adsorption and desorption of arsenate (As(V)) and arsenite (As(111)) oil calcite was investigated in a series of batch experiments in calcite-equilibrated solutions. The solutions covered a broad range of pH, alkalinity, calcium concentration and ionic strength. The initial arsenic...

Effects of Metal Ions on the Flotation of Apatite, Dolomite and Quartz

Directory of Open Access Journals (Sweden)

Yaoyang Ruan

2018-04-01

Full Text Available The effects of Ca2+, Mg2+, Al3+, and Fe3+ on the flotation behaviors of apatite, dolomite and quartz were investigated through a micro-flotation test, and the influence of calcium ions on the flotation of these minerals was further elucidated by solution chemistry study, zeta potential measurement, and X-ray photoelectron spectroscopy (XPS analyses. The results indicate that an appropriate amount of Ca2+ and Mg2+ can improve the floatability of apatite but had a negligible effect on the flotation performance of dolomite, whereas Al3+, Fe3+, and excessive amounts of Ca2+ decreased the recovery of apatite and dolomite. The studied metal cations can activate quartz at a particular pH. It can be inferred from solution chemistry and zeta potential measurement that the influence of metal ions on the flotation of different minerals should be attributed to the adsorption of various hydrolysis species on the mineral surfaces. XPS analyses reveal that calcium ions can enhance the adsorption of anionic collector on apatite and quartz surfaces, and there are no apparent changes to be observed on the surface of dolomite in the absence and presence of calcium ions at a concentration of 2.5 × 10−3 M, which was in good agreement with the micro-flotation results.

Using enteric pathogens to assess sources of fecal contamination in the Silurian Dolomite Aquifer: Preliminary results

Science.gov (United States)

Muldoon, Maureen A; Borchardt, Mark A.; Spencer, Susan K.; Hunt, Randall J.; Owens, David

2018-01-01

The fractured Silurian dolomite aquifer is an important, but vulnerable, source of drinking water in northeast Wisconsin (Sherrill in Geology and ground water in Door County, Wisconsin, with emphasis on contamination potential in the Silurian dolomite, 1978; Bradbury and Muldoon in Hydrogeology and groundwater monitoring of fractured dolomite in the Upper Door Priority Watershed, Door County, Wisconsin, 1992; Muldoon and Bradbury in Assessing seasonal variations in recharge and water quality in the Silurian aquifer in areas with thicker soil cover. p 45, 2010). Areas underlain by the Silurian dolomite aquifer are extremely vulnerable to groundwater contamination from various land-use activities, especially the disposal of human wastewater and dairy manure. Currently there is no consensus as to which source of wastewater generates the greater impact to the aquifer.

Effect of Mica and Hematite (001) Surfaces on the Precipitation of Calcite

OpenAIRE

Huifang Xu; Mo Zhou; Yihang Fang; H. Henry Teng

2018-01-01

The substrate effect of mica and hematite on the nucleation and crystallization of calcite was investigated using scanning electron microscope (SEM), X-ray diffraction (XRD), and electron backscatter diffraction (EBSD) methods. On mica, we found, in the absence of Mg2+, the substrates’ (001) surfaces with hexagonal and pseudo-hexagonal two-dimensional (2-D) structure can affect the orientation of calcite nucleation with calcite (001) ~// mica (001) and calcite (010) ~// mica (010) to be the m...

Selective Flotation of Calcite from Fluorite: A Novel Reagent Schedule

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Zhiyong Gao

2016-10-01

Full Text Available Fluorite is an important strategic mineral. In general, fluorite ores will contain a certain amount of calcite gangue mineral. Thus, they need to be separated from each other. For an economic separation, a reverse flotation process is used to float calcite gangue from fluorite. However, little information on the separation is available. In this study, a novel reagent schedule using citric acid (CA as the depressant, sodium fluoride (NaF as the regulator and sulfoleic acid (SOA as the collector, was developed to separate calcite from fluorite. The results demonstrated a high selectivity for the flotation of calcite from fluorite using this new reagent schedule. The best selective separation for a single mineral and mixed binary minerals was obtained when 200 mg/L of NaF, 50 mg/L of CA, and 6 mg/L of SOA were used at pH 9. In addition, a batch flotation experiment was carried out using a run-of-mine feed material. Selective separation was achieved with 85.18% calcite removal while only 11.2% of fluorite was lost. An attempt was made to understand the effect of the new reagent schedule on the flotation of calcite. The results from both microflotation and bench scale flotation demonstrated a great potential for industrial application using this novel reagent schedule to upgrade fluorite ore.

Evaluation of Various Synthesis Methods for Calcite-Precipitated Calcium Carbonate (PCC) Formation

International Nuclear Information System (INIS)

Ramakrishna, Chilakala; Thenepalli, Thriveni; Ahn, Ji Whan

2017-01-01

This review paper evaluates different kinds of synthesis methods for calcite precipitated calcium carbonates by using different materials. The various processing routes of calcite with different compositions are reported and the possible optimum conditions required to synthesize a desired particle sizes of calcite are predicted. This paper mainly focuses on that the calcite morphology and size of the particles by carbonation process using loop reactors. In this regard, we have investigated various parameters such as CO 2 flow rate, Ca (OH) 2 concentration, temperature, pH effect, reaction time and loop reactor mechanism with orifice diameter. The research results illustrate the formation of well-defined and pure calcite crystals with controlled crystal growth and particle size, without additives or organic solvents. The crystal growth and particle size can be controlled, and smaller sizes are obtained by decreasing the Ca (OH) 2 concentration and increasing the CO 2 flow rate at lower temperatures with suitable pH. The crystal structure of obtained calcite was characterized by using X-ray diffraction method and the morphology by scanning electron microscope (SEM). The result of x-ray diffraction recognized that the calcite phase of calcium carbonate was the dominating crystalline structure.

Surface Complexation Modeling of Calcite Zeta Potential Measurement in Mixed Brines for Carbonate Wettability Characterization

Science.gov (United States)

Song, J.; Zeng, Y.; Biswal, S. L.; Hirasaki, G. J.

2017-12-01

We presents zeta potential measurements and surface complexation modeling (SCM) of synthetic calcite in various conditions. The systematic zeta potential measurement and the proposed SCM provide insight into the role of four potential determining cations (Mg2+, SO42- , Ca2+ and CO32-) and CO2 partial pressure in calcite surface charge formation and facilitate the revealing of calcite wettability alteration induced by brines with designed ionic composition ("smart water"). Brines with varying potential determining ions (PDI) concentration in two different CO2 partial pressure (PCO2) are investigated in experiments. Then, a double layer SCM is developed to model the zeta potential measurements. Moreover, we propose a definition for contribution of charged surface species and quantitatively analyze the variation of charged species contribution when changing brine composition. After showing our model can accurately predict calcite zeta potential in brines containing mixed PDIs, we apply it to predict zeta potential in ultra-low and pressurized CO2 environments for potential applications in carbonate enhanced oil recovery including miscible CO2 flooding and CO2 sequestration in carbonate reservoirs. Model prediction reveals that pure calcite surface will be positively charged in all investigated brines in pressurized CO2 environment (>1atm). Moreover, the sensitivity of calcite zeta potential to CO2 partial pressure in the various brine is found to be in the sequence of Na2CO3 > Na2SO4 > NaCl > MgCl2 > CaCl2 (Ionic strength=0.1M).

Effect of dissolution kinetics on flotation response of calcite with oleate

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D. G. Horta

Full Text Available Abstract Phosphate flotation performance can be influenced by the dissolution kinetics of the minerals that compose the ore. The purpose of this work was to investigate the effect of dissolution kinetics on flotation response with oleate (collector of calcites from different origins and genesis. The calcite samples were first purified and characterized by x-ray Fluorescence (XRF and the Rietveld method applied to x-ray Diffractometry data (RXD. Experiments of calcite dissolution and microflotationwere performed at pH 8 and pH 10.The pH effect on the calcite dissolution and flotation indicates the possible influence of the carbonate/bicarbonate ions provided by the CO2 present in the air. In addition, the flotation response is greater as the dissolution increases, making more Ca2+ ions available to interact with collector molecules. This result corroborates the surface precipitation mechanism proposed foroleate adsorption on the calcite surface.

Interactions of U(VI), Nd, and Th(IV) at the Calcite-solution interface

International Nuclear Information System (INIS)

Carroll, S.A.; Dran, J.C.

1992-01-01

The interactions of U(VI), Nd, and Th(IV) at the calcite-solution interface at controlled pCO 2 (g) have been investigated by Rutherford backscattering (RBS), scanning electron microscopy (SEM) and energy dispersive (EDS) analyses of reacted calcite. Uranium precipitation at the calcite-solution interface was observed only for those experiments in which the initial [U(VI)] was greater than the solubility of rutherfordine, UO 2 CO 3 (s). At pH 8.0, flat radial uranium and calcium zoned precipitates form at the mineral-solution interface. At pH 4.3, uranium forms an anastomosing precipitate throughout the calcite surface. RBS analyses confirmed the SEM analyses showing that uranium forms a solid phase within the calcite surface, but formation of an uranium-calcium solid solution at depth is limited. In sharp contrast to U(VI), Nd is concentrated in the solid phase as individual neodymium-calcium carbonate crystals. Calcite and pure orthorhombic neodymium carbonate crystals dissolve at the expense of the formation of a more stable neodymium-calcium solid solution. In the presence of calcite, a thorium-calcium solid solution forms by exchanging Th for Ca in the calcite structure. Thorium precipitates in two linear trends which intersect each other at approximately 105deg C and 75deg C, parallel to calcite rhombohedral cleavage faces. (orig.)

Influence of water on clumped-isotope bond reordering kinetics in calcite

Science.gov (United States)

Brenner, Dana C.; Passey, Benjamin H.; Stolper, Daniel A.

2018-03-01

Oxygen self-diffusion in calcite and many other minerals is considerably faster under wet conditions relative to dry conditions. Here we investigate whether this "water effect" also holds true for solid-state isotope exchange reactions that alter the abundance of carbonate groups with multiple rare isotopes ('clumped' isotope groups) via the process of solid-state bond reordering. We present clumped-isotope reordering rates for optical calcite heated under wet, high-pressure (100 MPa) conditions. We observe only modest increases in reordering rates under such conditions compared with rates for the same material reacted in dry CO2 under low-pressure conditions. Activation energies under wet, high-pressure conditions are indistinguishable from those for dry, low-pressure conditions, while rate constants are resolvably higher (up to ∼3 times) for wet, high-pressure relative to dry, low-pressure conditions in most of our interpretations of experimental results. This contrasts with the water effect for oxygen self-diffusion in calcite, which is associated with lower activation energies, and diffusion coefficients that are ≥103 times higher compared with dry (pure CO2) conditions in the temperature range of this study (385-450 °C). The water effect for clumped-isotopes leads to calculated apparent equilibrium temperatures ("blocking temperatures") for typical geological cooling rates that are only a few degrees higher than those for dry conditions, while O self-diffusion blocking temperatures in calcite grains are ∼150-200 °C lower in wet conditions compared with dry conditions. Since clumped-isotope reordering is a distributed process that occurs throughout the mineral volume, our clumped-isotope results support the suggestion of Labotka et al. (2011) that the water effect in calcite does not involve major changes in bulk (volume) diffusivity, but rather is primarily a surface phenomenon that facilitates oxygen exchange between the calcite surface and external

Sorption and catalytic oxidation of Fe(II) at the surface of calcite

NARCIS (Netherlands)

Mettler, S.; Wolthers, M.; Charlet, L.; Von Gunten, U.

The effect of sorption and coprecipitation of Fe(II) with calcite on the kinetics of Fe(II) oxidation was investigated. The interaction of Fe(II) with calcite was studied experimentally in the absence and presence of oxygen. The sorption of Fe(II) on calcite occurred in two distinguishable steps:

The stratigraphy of the Malmani dolomite subgroup in the Carletonville area, Transvaal: genetic implications for lead-zinc mineralization

International Nuclear Information System (INIS)

Clay, A.N.

1986-01-01

The geological setting of a borehole intersection of lead-zinc mineralization in the Malmani Dolomite Subgroup in the Carletonville area is discussed. It is suggested that the lead and zinc ions were derived from the overlying shales, transported as bisulphide complexes in silica-enriched, alkaline solutions, and deposited during silicification in the upper part of the dolomite succession which contains relic evaporites. Lead isotope data suggests that the known lead-zinc deposits in the Transvaal sequence are not of major importance. However, the dolomites are regarded as very probable hosts for Mississippi Valley type base metal deposits and offer important exploration targets. This study includes lead isotopic data. Lead isotope compositions and model lead ages for galenas in the zinc deposits are shown. It is concluded that the leads have undergone either a two-stage evolution process, or have mixed with 206 Pb-enriched ores. Model ages suggest that the lead was derived from an approximate 2,7 Ga source and that mineralization took place at 1,7 Ga

Incorporation of Mg and Sr in calcite of cultured benthic foraminifera: impact of calcium concentration and associated calcite saturation state

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M. Raitzsch

2010-03-01

Full Text Available We investigated the effect of the calcium concentration in seawater and thereby the calcite saturation state (Ω on the magnesium and strontium incorporation into benthic foraminiferal calcite under laboratory conditions. For this purpose individuals of the shallow-water species Heterostegina depressa (precipitating high-Mg calcite, symbiont-bearing and Ammonia tepida (low-Mg calcite, symbiont-barren were cultured in media under a range of [Ca²⁺], but similar Mg/Ca ratios. Trace element/Ca ratios of newly formed calcite were analysed with Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS and normalized to the seawater elemental composition using the equation D_TE=(TE/Ca_calcite/(TE/Ca_seawater. The culturing study shows that D_Mg of A. tepida significantly decreases with increasing Ω at a gradient of −4.3×10⁻⁵ per Ω unit. The D_Sr value of A. tepida does not change with Ω, suggesting that fossil Sr/Ca in this species may be a potential tool to reconstruct past variations in seawater Sr/Ca. Conversely, D_Mg of H. depressa shows only a minor decrease with increasing Ω, while D_Sr increases considerably with Ω at a gradient of 0.009 per Ω unit. The different responses to seawater chemistry of the two species may be explained by a difference in the calcification pathway that is, at the same time, responsible for the variation in the total Mg incorporation between the two species. Since the Mg/Ca ratio in H. depressa is 50–100 times higher than that of A. tepida, it is suggested that the latter exhibits a mechanism that decreases the Mg/Ca ratio of the calcification fluid, while the high-Mg calcite forming species may not have this physiological tool. If the dependency of Mg incorporation on seawater [Ca²⁺] is also valid for deep

Hydrochemical controls on aragonite versus calcite precipitation in cave dripwaters

Science.gov (United States)

Rossi, Carlos; Lozano, Rafael P.

2016-11-01

Despite the paleoclimatic relevance of primary calcite to aragonite transitions in stalagmites, the relative role of fluid Mg/Ca ratio, supersaturation and CO32- concentration in controlling such transitions is still incompletely understood. Accordingly, we have monitored the hydrochemistry of 50 drips and 8 pools that are currently precipitating calcite and/or aragonite in El Soplao and Torca Ancha Caves (N. Spain), investigating the mineralogy and geochemistry of the CaCO3 precipitates on the corresponding natural speleothem surfaces. The data reveal that, apart from possible substrate effects, dripwater Mg/Ca is the only obvious control on CaCO3 polymorphism in the studied stalagmites and pools, where calcite- and aragonite-precipitating dripwaters are separated by an initial (i.e. at stalactite tips) Mg/Ca threshold at ≈1.1 mol/mol. Within the analyzed ranges of pH (8.2-8.6), CO32- concentration (1-6 mg/L), supersaturation (SIaragonite: 0.08-1.08; SIcalcite: 0.23-1.24), drip rate (0.2-81 drops/min) and dissolved Zn (6-90 μg/L), we observe no unequivocal influence of these parameters on CaCO3 mineralogy. Despite the almost complete overlapping supersaturations of calcite- and aragonite-precipitating waters, the latter are on average less supersaturated because the waters having Mg/Ca above ∼1.1 have mostly achieved such high ratios by previously precipitating calcite. Both calcite and aragonite precipitated at or near oxygen isotopic equilibrium, and Mg incorporation into calcite was consistent with literature-based predictions, indicating that in the studied cases CaCO3 precipitation was not significantly influenced by strong kinetic effects. In the studied cases, the calcites that precipitate at ∼11 °C from dripwaters with initial Mg/Ca approaching ∼1.1 incorporate ∼5 mol% MgCO3, close to the published value above which calcite solubility exceeds aragonite solubility, suggesting that aragonite precipitation in high-relative-humidity caves is

Evaluation of Various Synthesis Methods for Calcite-Precipitated Calcium Carbonate (PCC) Formation

Energy Technology Data Exchange (ETDEWEB)

Ramakrishna, Chilakala [Hanil Cement Corporation, Danyang (Korea, Republic of); Thenepalli, Thriveni; Ahn, Ji Whan [Korea Institute of Geoscience and Mineral Resources, Daejeon (Korea, Republic of)

2017-06-15

This review paper evaluates different kinds of synthesis methods for calcite precipitated calcium carbonates by using different materials. The various processing routes of calcite with different compositions are reported and the possible optimum conditions required to synthesize a desired particle sizes of calcite are predicted. This paper mainly focuses on that the calcite morphology and size of the particles by carbonation process using loop reactors. In this regard, we have investigated various parameters such as CO{sub 2} flow rate, Ca (OH){sub 2} concentration, temperature, pH effect, reaction time and loop reactor mechanism with orifice diameter. The research results illustrate the formation of well-defined and pure calcite crystals with controlled crystal growth and particle size, without additives or organic solvents. The crystal growth and particle size can be controlled, and smaller sizes are obtained by decreasing the Ca (OH){sub 2} concentration and increasing the CO{sub 2} flow rate at lower temperatures with suitable pH. The crystal structure of obtained calcite was characterized by using X-ray diffraction method and the morphology by scanning electron microscope (SEM). The result of x-ray diffraction recognized that the calcite phase of calcium carbonate was the dominating crystalline structure.

EPR, UV-Visible, and Near-Infrared Spectroscopic Characterization of Dolomite

Directory of Open Access Journals (Sweden)

S. Lakshmi Reddy

2008-01-01

Full Text Available Dolomite mineral samples having white and light green colors of Indian origin have been characterized by EPR, optical, and NIR spectroscopy. The optical spectrum exhibits a number of electronic bands due to presence of Fe(III ions in the mineral. From EPR studies, the parameters of g for Fe(III and g,A, and D for Mn(II are evaluated and the data confirm that the ions are in distorted octahedron. Optical absorption studies reveal that Fe(III is in distorted octahedron. The bands in NIR spectra are due to the overtones and combinations of water molecules. Thus EPR and optical absorption spectral studies have proven useful for the study of the solid state chemistry of dolomite.

Dolomitization in the diagenetic history of the Štramberg limestones

Czech Academy of Sciences Publication Activity Database

Lintnerová, O.; Knietl, M.; Reháková, D.; Skupien, P.; Vašíček, Zdeněk

2008-01-01

Roč. 34, 3/1 (2008), s. 191-192 ISSN 0138-0974 Institutional research plan: CEZ:AV0Z30860518 Keywords : Štramberk Limestone * dolomitization * dedolomitization Subject RIV: DB - Geology ; Mineralogy

Early diagenetic dolomitization and dedolomitization of Late Jurassic and earliest Cretaceous platform carbonates: A case study from the Jura Mountains (NW Switzerland, E France)

Science.gov (United States)

Rameil, Niels

2008-12-01

Early diagenetic dolomitization is a common feature in cyclic shallow-water carbonates throughout the geologic record. After their generation, dolomites may be subject to dedolomitization (re-calcification of dolomites), e.g. by contact with meteoric water during emersion. These patterns of dolomitization and subsequent dedolomitization frequently play a key role in unravelling the development and history of a carbonate platform. On the basis of excellent outcrops, detailed logging and sampling and integrating sedimentological work, high-resolution sequence stratigraphic interpretations, and isotope analyses (O, C), conceptual models on early diagenetic dolomitization and dedolomitization and their underlying mechanisms were developed for the Upper Jurassic / Lower Cretaceous Jura platform in north-western Switzerland and eastern France. Three different types of early diagenetic dolomites and two types of dedolomites were observed. Each is defined by a distinct petrographic/isotopic signature and a distinct spatial distribution pattern. Different types of dolomites are interpreted to have been formed by different mechanisms, such as shallow seepage reflux, evaporation on tidal flats, and microbially mediated selective dolomitization of burrows. Depending on the type of dolomite, sea water with normal marine to slightly enhanced salinities is proposed as dolomitizing fluid. Based on the data obtained, the main volume of dolomite was precipitated by a reflux mechanism that was switched on and off by high-frequency sea-level changes. It appears, however, that more than one dolomitization mechanism was active (pene)contemporaneously or several processes alternated in time. During early diagenesis, percolating meteoric waters obviously played an important role in the dedolomitization of carbonate rocks that underlie exposure surfaces. Cyclostratigraphic interpretation of the sedimentary succession allows for estimates on the timing of early diagenetic (de)dolomitization

Conditions of uranium-bearing calcite formation in ore-enclosing sediments of the Semizbaj deposit (Kazakhstan)

International Nuclear Information System (INIS)

Kondrat'eva, I.A.; Maksimova, I.G.; Dojnikova, O.I.

1995-01-01

Consideration is given to results of investigation into uranium-bearing calcite, forming the cement of gravelly-sandy rocks of the Semizbaj uranium deposit. Core sampling in prospecting boreholes were used to establish geological conditions, place and time of uranium-bearing calcite formation. Calcite was investigated by optical, electron-microscope and radiographic methods. It is shown that uranium in calcite doesn't form its own mineral phase and exists in scattered state. Uranium in calcite-bearing minerals is present in isomorphic form. Uranium content in calcite was equal to 0.009-0.15 %. It is proposed that mineralization, formed in sedimentary rocks by processes of ground-stratum oxidation, is the source of uranium, enriching calcite. refs., 5 figs., 2 tabs

Monitoring of Calcite Precipitation in Hardwater Lakes with Multi-Spectral Remote Sensing Archives

Directory of Open Access Journals (Sweden)

Iris Heine

2017-01-01

Full Text Available Calcite precipitation is a common phenomenon in calcium-rich hardwater lakes during spring and summer, but the number and spatial distribution of lakes with calcite precipitation is unknown. This paper presents a remote sensing based method to observe calcite precipitation over large areas, which are an important prerequisite for a systematic monitoring and evaluation of restoration measurements. We use globally archived satellite remote sensing data for a retrospective systematic assessment of past multi-temporal calcite precipitation events. The database of this study consists of 205 data sets that comprise freely available Landsat and Sentinel 2 data acquired between 1998 and 2015 covering the Northeast German Plain. Calcite precipitation is automatically identified using the green spectra and the metric BGR area, the triangular area between the blue, green and red reflectance value. The validation is based on field measurements of CaCO3 concentrations at three selected lakes, Feldberger Haussee, Breiter Luzin and Schmaler Luzin. The classification accuracy (0.88 is highest for calcite concentrations ≥0.7 mg/L. False negative results are caused by the choice of a conservative classification threshold. False positive results can be explained by already increased calcite concentrations. We successfully transferred the developed method to 21 other hardwater lakes in Northeast Germany. The average duration of lakes with regular calcite precipitation is 37 days. The frequency of calcite precipitation reaches from single time detections up to detections nearly every year. False negative classification results and gaps in Landsat time series reduce the accuracy of frequency and duration monitoring, but in future the image density will increase by acquisitions of Sentinel-2a (and 2b. Our study tested successfully the transfer of the classification approach to Sentinel-2 images. Our study shows that 15 of the 24 lakes have at least one phase of

Transformation of Mg-bearing amorphous calcium carbonate to Mg-calcite - In situ monitoring

Science.gov (United States)

Purgstaller, Bettina; Mavromatis, Vasileios; Immenhauser, Adrian; Dietzel, Martin

2016-02-01

The formation of Mg-bearing calcite via an amorphous precursor is a poorly understood process that is of relevance for biogenic and abiogenic carbonate precipitation. In order to gain an improved insight on the controls of Mg incorporation in calcite formed via an Mg-rich amorphous calcium carbonate (Mg-ACC) precursor, the precipitation of Mg-ACC and its transformation to Mg-calcite was monitored by in situ Raman spectroscopy. The experiments were performed at 25.0 ± 0.03 °C and pH 8.3 ± 0.1 and revealed two distinct pathways of Mg-calcite formation: (i) At initial aqueous Mg/Ca molar ratios ⩽ 1:6, Mg-calcite formation occurs via direct precipitation from solution. (ii) Conversely, at higher initial Mg/Ca molar ratios, Mg-calcite forms via an intermediate Mg-rich ACC phase. In the latter case, the final product is a calcite with up to 20 mol% Mg. This Mg content is significant higher than that of the Mg-rich ACC precursor phase. Thus, a strong net uptake of Mg ions from the solution into the crystalline precipitate throughout and also subsequent to ACC transformation is postulated. Moreover, the temporal evolution of the geochemical composition of the reactive solution and the Mg-ACC has no significant effect on the obtained ;solubility product; of Mg-ACC. The enrichment of Mg in calcite throughout and subsequent to Mg-ACC transformation is likely affected by the high aqueous Mg/Ca ratio and carbonate alkalinity concentrations in the reactive solution. The experimental results have a bearing on the formation mechanism of Mg-rich calcites in marine early diagenetic environments, where high carbonate alkalinity concentrations are the rule rather than the exception, and on the insufficiently investigated inorganic component of biomineralisation pathways in many calcite secreting organisms.

Investigating calcite growth rates using a quartz crystal microbalance with dissipation (QCM-D)

Science.gov (United States)

Cao, Bo; Stack, Andrew G.; Steefel, Carl I.; DePaolo, Donald J.; Lammers, Laura N.; Hu, Yandi

2018-02-01

Calcite precipitation plays a significant role in processes such as geological carbon sequestration and toxic metal sequestration and, yet, the rates and mechanisms of calcite growth under close to equilibrium conditions are far from well understood. In this study, a quartz crystal microbalance with dissipation (QCM-D) was used for the first time to measure macroscopic calcite growth rates. Calcite seed crystals were first nucleated and grown on sensors, then growth rates of calcite seed crystals were measured in real-time under close to equilibrium conditions (saturation index, SI = log ({Ca2+}/{CO32-}/Ksp) = 0.01-0.7, where {i} represent ion activities and Ksp = 10-8.48 is the calcite thermodynamic solubility constant). At the end of the experiments, total masses of calcite crystals on sensors measured by QCM-D and inductively coupled plasma mass spectrometry (ICP-MS) were consistent, validating the QCM-D measurements. Calcite growth rates measured by QCM-D were compared with reported macroscopic growth rates measured with auto-titration, ICP-MS, and microbalance. Calcite growth rates measured by QCM-D were also compared with microscopic growth rates measured by atomic force microscopy (AFM) and with rates predicted by two process-based crystal growth models. The discrepancies in growth rates among AFM measurements and model predictions appear to mainly arise from differences in step densities, and the step velocities were consistent among the AFM measurements as well as with both model predictions. Using the predicted steady-state step velocity and the measured step densities, both models predict well the growth rates measured using QCM-D and AFM. This study provides valuable insights into the effects of reactive site densities on calcite growth rate, which may help design future growth models to predict transient-state step densities.

Lithostratigraphy of Upper Ordovician strata exposed in Kentucky

Science.gov (United States)

Weir, Gordon Whitney; Peterson, Warren Lee; Swadley, W.C.

1984-01-01

Creek Limestone in the western and central parts. In east-central Kentucky, the Grant Lake is classified as a member of the Ashlock Formation, an assemblage of lithologically distinct units that were combined to facilitate mapping in the southeastern and southern part of the region. The Ashlock consists of the following members, in ascending order: The Tate (calcitic and dolomitic mudstone), the Grant Lake, the Gilbert (micrograined limestone and shale), the Stingy Creek (nodular-bedded mudstone and limestone), the Terrill (dolomitic and calcitic mudstone), the Sunset (micrograined limestone), and the Reba (nodular-bedded limestone and shale). The Bull Fork Formation, which overlies the Grant Lake Limestone, is made up of subequal amounts of thin-bedded highly fossiliferous limestone and shale; limestone makes up about 80 percent of the basal part of the formation and decreases in abundance irregularly upward to only 20 percent of the top part. On the east side of the Blue Grass region, the Bull Fork grades into the Reba Member of the Ashlock Formation; on the west side, it grades into the Grant Lake. The uppermost formation in the region is the Drakes Formation, which in east-central Kentucky consists of the Rowland Member (calcitic to dolomitic mudstone) overlain by the Preachersville Member (dolomitic to calcitic mudstone and dolomite and dolomitic siltstone). In northeast Kentucky, the Drakes is represented by only the Preachersville Member. In most of central and north-central Kentucky, the formation consists of three members: the Rowland at the base (dolomitic mudstone to muddy limestone), the Bardstown (fossiliferous limestone and shale), and the Saluda Dolomite (dolomite, in part calcitic and muddy). In northern north-central Kentucky, the Drakes is represented by only the Saluda Dolomite Member. The top of the Ordovician sequence in the Blue Grass region is generally formed by members of the Drakes Formation, which are overlain by str

The coprecipitation of Sr2+ with calcite at 250C and 1 atm

International Nuclear Information System (INIS)

Pingitore, N.E. Jr.; Eastman, M.P.

1986-01-01

The incorporation of Sr 2+ into calcite at earth surface aqueous conditions is affected by the absolute concentration of Sr 2+ , the presence of Ba 2+ and NaCl in the solution and the rate of precipitation. At solution ratios (molar) of Sr 2+ to Ca 2+ in the low 10 -3 range, which yield calcites with several hundred ppm Sr 2+ , kappasub(calcite) sup(Sr) typically assumes a value between 0.10 and 0.20. Above these concentrations the value of kappasub(calcite) sup(Sr) drops to approximately 0.06. Furthermore, if minor amounts of Ba 2+ or large amounts of Na + (0.48 M) are added to a dilute Sr 2+ solution, a value around 0.06 for kappasub(calcite)sup(Sr) is found. This 'strontium concentration effect' and the associated 'competitive cation effect' suggest that small amounts of Sr 2+ may be incorporated into a limited number of nonlattice sites in calcite. Incorporation of Sr 2+ into these sites, presumably defects, noticeably affects kappasub(calcite)sup(Sr) only at low Sr 2+ concentrations and in the absence of competition from other large cations. An increase in kappasub(calcite)sup(Sr) with rate of precipitation, qualitatively similar to that found in other studies, was observed only when precipitation times were decreased from days to hours. For many geologic settings a partition coefficient for Sr 2+ into calcite of 0.06 appears appropriate, but there are situations - very low Sr 2+ concentrations, the presence of Mg 2+ , and fast precipitation rates - in which a larger value might better approximate natural partitioning. (author)

Prediction of calcite Cement Distribution in Shallow Marine Sandstone Reservoirs using Seismic Data

Energy Technology Data Exchange (ETDEWEB)

Bakke, N.E.

1996-12-31

This doctoral thesis investigates how calcite cemented layers can be detected by reflection seismic data and how seismic data combined with other methods can be used to predict lateral variation in calcite cementation in shallow marine sandstone reservoirs. Focus is on the geophysical aspects. Sequence stratigraphy and stochastic modelling aspects are only covered superficially. Possible sources of calcite in shallow marine sandstone are grouped into internal and external sources depending on their location relative to the presently cemented rock. Well data and seismic data from the Troll Field in the Norwegian North Sea have been analysed. Tuning amplitudes from stacks of thin calcite cemented layers are analysed. Tuning effects are constructive or destructive interference of pulses resulting from two or more closely spaced reflectors. The zero-offset tuning amplitude is shown to depend on calcite content in the stack and vertical stack size. The relationship is found by regression analysis based on extensive seismic modelling. The results are used to predict calcite distribution in a synthetic and a real data example. It is found that describing calcite cemented beds in shallow marine sandstone reservoirs is not a deterministic problem. Hence seismic inversion and sequence stratigraphy interpretation of well data have been combined in a probabilistic approach to produce models of calcite cemented barriers constrained by a maximum amount of information. It is concluded that seismic data can provide valuable information on distribution of calcite cemented beds in reservoirs where the background sandstones are relatively homogeneous. 63 refs., 78 figs., 10 tabs.

Magnetite-apatite-dolomitic rocks of Ust-Chulman (Aldan shield, Russia): Seligdar-type carbonatites?

Science.gov (United States)

Prokopyev, Ilya R.; Doroshkevich, Anna G.; Redina, Anna A.; Obukhov, Andrey V.

2018-04-01

The Ust-Chulman apatite ore body is situated within the Nimnyrskaya apatite zone at the Aldan shield in Russia. The latest data confirm the carbonatitic origin of the Seligdar apatite deposit (Prokopyev et al. in Ore Geol Rev 81:296-308, 2017). The results of our investigations demonstrate that the magnetite-apatite-dolomitic rocks of the Ust-Chulman are highly similar to Seligdar-type dolomitic carbonatites in terms of the mineralogy and the fluid regime of formation. The ilmenite and spinel mineral phases occur as solid solutions with magnetite, and support the magmatic origin of the Ust-Chulman ores. The chemical composition of REE- and SO3-bearing apatite crystals and, specifically, monazite-(Ce) mineralisation and the formation of Nb-rutile, late hydrothermal sulphate minerals (barite, anhydrite) and haematite are typical for carbonatite complexes. The fluid inclusions study revealed similarities to the evolutionary trend of the Seligdar carbonatites that included changes of the hydrothermal solutions from highly concentrated chloride to medium-low concentrated chloride-sulphate and oxidized carbonate-ferrous.

Muddy and dolomitic rip-up clasts in Triassic fluvial sandstones: Origin and impact on potential reservoir properties (Argana Basin, Morocco)

Science.gov (United States)

Henares, Saturnina; Arribas, Jose; Cultrone, Giuseppe; Viseras, Cesar

2016-06-01

The significance of rip-up clasts as sandstone framework grains is frequently neglected in the literature being considered as accessory components in bulk sandstone composition. However, this study highlights the great value of muddy and dolomitic rip-up clast occurrence as: (a) information source about low preservation potential from floodplain deposits and (b) key element controlling host sandstone diagenetic evolution and thus ultimate reservoir quality. High-resolution petrographic analysis on Triassic fluvial sandstones from Argana Basin (T6 and T7/T8 units) highlights the significance of different types of rip-up clasts as intrabasinal framework components of continental sediments from arid climates. On the basis of their composition and ductility, three main types are distinguished: (a) muddy rip-up clasts, (b) dolomitic muddy rip-up clasts and (c) dolomite crystalline rip-up clasts. Spatial distribution of different types is strongly facies-related according to grain size. Origin of rip-up clasts is related to erosion of coeval phreatic dolocretes, in different development stages, and associated muddy floodplain sediments. Cloudy cores with abundant inclusions and clear outer rims of dolomite crystals suggest a first replacive and a subsequent displacive growth, respectively. Dolomite crystals are almost stoichiometric. This composition is very similar to that of early sandstone dolomite cement, supporting phreatic dolocretes as dolomite origin in both situations. Sandstone diagenesis is dominated by mechanical compaction and dolomite cementation. A direct correlation exists between: (1) muddy rip-up clast abundance and early reduction of primary porosity by compaction with irreversible loss of intergranular volume (IGV); and (2) occurrence of dolomitic rip-up clasts and dolomite cement nucleation in host sandstone, occluding adjacent pores but preserving IGV. Both processes affect reservoir quality by generation of vertical and 3D fluid flow baffles and

Molecular ordering of ethanol at the calcite surface.

Science.gov (United States)

Pasarín, I S; Yang, M; Bovet, N; Glyvradal, M; Nielsen, M M; Bohr, J; Feidenhans'l, R; Stipp, S L S

2012-02-07

To produce biominerals, such as shells, bones, and teeth, living beings create organic compounds that control the growth of the solid phase. Investigating the atomic scale behavior of individual functional groups at the mineral-fluid interface provides fundamental information that is useful for constructing accurate predictive models for natural systems. Previous investigations of the activity of coccolith-associated polysaccharides (CAP) on calcite, using atomic force microscopy (AFM) [Henriksen, K., Young, J. R., Bown, P. R., and Stipp, S. L. S. Palentology 2004, 43 (Part 3), 725-743] and molecular dynamics (MD) modeling [Yang, M., Stipp, S. L. S., and Harding, J. H. Cryst. Growth Des. 2008, 8 (11), 4066-4074], have suggested that OH functional groups control polysaccharide attachment. The purpose of this work was to characterize, using X-ray reflectivity (XR) combined with molecular dynamics (MD) simulations, the structuring on calcite of a layer of the simplest carbon chain molecule that contains an OH group, ethanol (CH(3)-CH(2)-OH). We found evidence that EtOH forms a highly ordered structure at the calcite surface, where the first layer molecules bond with calcite. The ethanol molecules stand up perpendicularly at the interface or nearly so. As a consequence, the fatty, CH(3) ends form a new surface, about 6 Å from the termination of the bulk calcite, and beyond that, there is a thin gap where ethanol density is low. Following is a more disordered layer that is two to three ethanol molecules thick, about 14 Å, where density more resembles that of bulk liquid ethanol. The good agreement between theory and experiment gives confidence that a theoretical approach can offer information about behavior in more complex systems.

The potential for phosphorus pollution remediation by calcite precipitation in UK freshwaters

Directory of Open Access Journals (Sweden)

C. Neal

2001-01-01

Full Text Available This paper examines the potential for calcium carbonate to reduce phosphate pollution in freshwaters by co-precipitation, a process known as a "self cleansing mechanism". Calcium carbonate saturation levels and phosphate concentrations (SRP - soluble reactive phosphate across the major eastern UK river basins are examined to test for solubility controls. The study shows that calcite saturation varies for each catchment as a function of flow and biological activity rather than by direct regulation by SRP. Indeed, there is no evidence, for any of the rivers studied, that calcite solubility controls hold. However, for groundwater and groundwater-fed springs in the Chalk of the Thames basin, calcite saturation is observed with associated low SRP levels. A self-cleansing mechanism may well be operative within the Chalk due to two factors. Firstly, there is a high potential for nucleation on the calcite micro-crystals in the aquifer. Secondly, there are within aquifer reactions that remove the calcite nucleating inhibitors (SRP and dissolved organic carbon, DOC to levels lower than those occurring within the rivers do. These inhibitors enter the catchment at very high concentrations in association with agricultural pollution (fertilizer application and animal slurry and household contamination (e.g. sewage sources from septic tanks. Under low flow conditions, when the saturation index for calcite is at its highest, so too is the concentration of the nucleation inhibitor SRP. Companion work shows that calcite precipitation can occur at the water-sediment interface of the river and this may involve SRP removal. The data, as a whole, define an apparent bound for calcite solubility control where in the presence of nucleating centres, SRP must be less than 4 mM-P l-1 and DOC must be less than 150 mM-C l-1: a condition that does not seem to pertain within most UK rivers. Keywords: calcite, calcium carbonate, phosphate, soluble reactive phosphate, dissolved

Speciation of As in calcite by micro-XAFS: Implications for remediation of As contamination in groundwater

International Nuclear Information System (INIS)

Yokoyama, Y; Takahashi, Y; Iwatsuki, T; Terada, Y

2013-01-01

To evaluate the role of calcite as a host phase of arsenic (As) in As-contaminated groundwater, distribution behavior of Asbetween natural calcite and groundwater in deep underground was investigated based on As oxidation state. Speciation analyses of As in natural calcite by μ-XRF-XAFS analyses showed (i) preferentialarsenate uptake by calcite, and (ii) promptness of arsenate uptake by minor iron (Fe) carbonate minerals coprecipitated with calcite. These findings suggest that the effect of calcite on As remediation of the As-contamination systems stronglydepends on arsenite to arsenate ratio (i.e., redox condition) in groundwater, and maybe governed bythe amount of Fe coprecipitated with calcite.

Organic geochemistry and stable isotope composition of New Zealand carbonate concretions and calcite fracture fills

International Nuclear Information System (INIS)

Pearson, M.J.; Nelson, C.S.

2005-01-01

Carbonate concretion bodies, representing a number of morphological types, and associated calcite fracture fills, mainly from New Zealand, have been studied both organically and inorganically. Extracted organic material is dominated by a complex polymeric dark brown highly polar fraction with a subordinate less polar and lighter coloured lipid fraction. The relative proportion of the two fractions is the principal control on the colour of fracture fill calcites. Concretions are classified mainly by reference to their carbonate stable carbon and oxygen isotope and cation composition. Typical subspherical calcitic septarian concretions, such as those in the Paleocene Moeraki and the Eocene Rotowaro Siltstones, contain carbon derived mainly by bacterial sulfate reduction in marine strata during early diagenesis. Other concretions, including a septarian calcitic type from the Northland Allochthon, have a later diagenetic origin. Siderite concretions, abundant in the nonmarine Waikato Coal Measures, are typically dominated by methanogenic carbon, whereas paramoudra-like structures from the Taranaki Miocene have the most extreme carbon isotope compositions, probably resulting from methane formation or oxidation in fluid escape conduits. Lipids from concretion bodies and most fracture fill calcites contain significant concentrations of fatty acids. Concretion bodies dominated by bimodally distributed n-fatty acids with strong even-over-odd preference, in which long chain n-acids are of terrestrial origin, have very low hydrocarbon biomarker maturities. Concretion bodies that lack long chain n-acids often have higher apparent biomarker maturity and prominent alpha-omega diacids. Such diacids are abundant in fracture fill calcites at Rotowaro, especially where calcite infills the septaria of a siderite concretion in the non-marine Waikato Coal Measures, and support the view that fluid transport resulted in carbonate entrapment of the fracture-hosted acids. Diacids also

An XRPD and EPR spectroscopy study of microcrystalline calcite bioprecipitated by Bacillus subtilis

Science.gov (United States)

Perito, B.; Romanelli, M.; Buccianti, A.; Passaponti, M.; Montegrossi, G.; Di Benedetto, F.

2018-05-01

We report in this study the first XRPD and EPR spectroscopy characterisation of a biogenic calcite, obtained from the activity of the bacterium Bacillus subtilis. Microcrystalline calcite powders obtained from bacterial culture in a suitable precipitation liquid medium were analysed without further manipulation. Both techniques reveal unusual parameters, closely related to the biological source of the mineral, i.e., to the bioprecipitation process and in particular to the organic matrix observed inside calcite. In detail, XRPD analysis revealed that bacterial calcite has slightly higher c/a lattice parameters ratio than abiotic calcite. This correlation was already noticed in microcrystalline calcite samples grown by bio-mineralisation processes, but it had never been previously verified for bacterial biocalcites. EPR spectroscopy evidenced an anomalously large value of W 6, a parameter that can be linked to occupation by different chemical species in the next nearest neighbouring sites. This parameter allows to clearly distinguish bacterial and abiotic calcite. This latter achievement was obtained after having reduced the parameters space into an unbiased Euclidean one, through an isometric log-ratio transformation. We conclude that this approach enables the coupled use of XRPD and EPR for identifying the traces of bacterial activity in fossil carbonate deposits.

Mechanism of Calcite Co-Orientation in the Sea Urchin Tooth

Energy Technology Data Exchange (ETDEWEB)

Killian, Christopher; Metzler, Rebecca; Gong, Y. U. T.; Olson, Ian; Aizenberg, Joanna; Politi, Yael; Wilt, Fred; Scholl, Andreas; Young, Anthony; Doran, Andrew; Kunz, Martin; Tamura, Nobumichi; Coppersmith, Susan; Gilbert, P. U. P. A.

2009-12-01

Sea urchin teeth are remarkable and complex calcite structures, continuously growing at the forming end and self-sharpening at the mature grinding tip. The calcite (CaCO{sub 3}) crystals of tooth components, plates, fibers, and a high-Mg polycrystalline matrix, have highly co-oriented crystallographic axes. This ability to co-orient calcite in a mineralized structure is shared by all echinoderms. However, the physico-chemical mechanism by which calcite crystals become co-oriented in echinoderms remains enigmatic. Here, we show differences in calcite c-axis orientations in the tooth of the purple sea urchin (Strongylocentrotus purpuratus), using high-resolution X-ray photoelectron emission spectromicroscopy (X-PEEM) and microbeam X-ray diffraction ({mu}XRD). All plates share one crystal orientation, propagated through pillar bridges, while fibers and polycrystalline matrix share another orientation. Furthermore, in the forming end of the tooth, we observe that CaCO{sub 3} is present as amorphous calcium carbonate (ACC). We demonstrate that co-orientation of the nanoparticles in the polycrystalline matrix occurs via solid-state secondary nucleation, propagating out from the previously formed fibers and plates, into the amorphous precursor nanoparticles. Because amorphous precursors were observed in diverse biominerals, solid-state secondary nucleation is likely to be a general mechanism for the co-orientation of biomineral components in organisms from different phyla.

Sea urchin tooth mineralization: Calcite present early in the aboral plumula

Science.gov (United States)

Stock, Stuart R.; Veis, Arthur; Xiao, Xianghui; Almer, Jonathan D.; Dorvee, Jason R.

2012-01-01

In both vertebrate bone, containing carbonated hydroxyapatite as the mineral phase, and in invertebrate hard tissue comprised of calcium carbonate, a popular view is that the mineral phase develops from a long-lived amorphous precursor which later transforms into crystal form. Important questions linked to this popular view are: When and where is the crystallized material formed, and is amorphous solid added subsequently to the crystalline substrate? Sea urchin teeth, in which the earliest mineral forms within isolated compartments, in a time and position dependent manner, allow direct investigation of the timing of crystallization of the calcite primary plates. Living teeth of the sea urchin Lytechinus variegatus, in their native coelomic fluid, were examined by high-energy synchrotron x-ray diffraction. The diffraction data show that calcite is present in the most aboral portions of the plumula, representing the very earliest stages of mineralization, and that this calcite has the same crystal orientation as in the more mature adoral portions of the same tooth. Raman spectroscopy of the aboral plumula confirms the initial primary plate mineral material is calcite and does not detect amorphous calcium carbonate; in the more mature adoral incisal flange, it does detect a broader calcite peak, consistent with two or more magnesium compositions. We hypothesize that some portion of each syncytial membrane in the plumula provides the information for nucleation of identically oriented calcite crystals that subsequently develop to form the complex geometry of the single crystal sea urchin tooth. PMID:22940703

A study on the coprecipitation of arsenite and arsenate into calcite coupled with the determination of oxidation states of arsenic both in calcite and water

International Nuclear Information System (INIS)

Yokoyama, Yuka; Takahashi, Yoshio; Mitsunobu, Satoshi; Tanaka, Kazuya; Itai, Takaaki

2009-01-01

It was found that the amount of arsenite incorporated into calcite is much less than that of arsenate. The result suggests that the sequestration of arsenic by coprecipitation with calcite cannot be an important chemical process under reducing conditions such as in groundwater where arsenite is the dominant arsenic species. (author)

Raman spectroscopic study of calcite III to aragonite transformation under high pressure and high temperature

Science.gov (United States)

Liu, Chuanjiang; Zheng, Haifei; Wang, Duojun

2017-10-01

In our study, a series of Raman experiments on the phase transition of calcite at high pressure and high temperature were investigated using a hydrothermal diamond anvil cell and Raman spectroscopy technique. It was found that calcite I transformed to calcite II and calcite III at pressures of 1.62 and 2.12 GPa and room temperature. With increasing temperature, the phase transition of calcite III to aragonite occurred. Aragonite was retained upon slowly cooling of the system, indicating that the transition of calcite III to aragonite was irreversible. Based on the available data, the phase boundary between calcite III and aragonite was determined by the following relation: P(GPa) = 0.013 × T(°C) + 1.22 (100°C ≤ T ≤ 170°C). It showed that the transition pressure linearly rose with increasing temperature. A better understanding of the stability of calcite III and aragonite is of great importance to further explore the thermodynamic behavior of carbonates and carbon cycling in the mantle.

FORMATION OF CALCITE AND SILICA FROM PERCOLATION IN A HYDROLOGICALLY UNSATURATED SETTING, YUCCA MOUNTAIN, NEVADA

International Nuclear Information System (INIS)

Paces, J.B.; Whelan, J.F.; Peterman, Z.E.; Marshall, B.D.

2000-01-01

Geological, mineralogical, chemical, and isotopic evidence from coatings of calcite and silica on open fractures and lithophysal cavities within welded tuffs at Yucca Mountain indicate an origin from meteoric water percolating through a thick (500 to 700 m) unsaturated zone (UZ) rather than from pulses of ascending ground water. Geologic evidence for a UZ setting includes the presence of coatings in only a small percentage of cavities, the restriction of coatings to fracture footwalls and cavity floors, and an absence of mineral high-water marks indicative of water ponding. Systematic mineral sequences (early calcite, followed by chalcedony with minor quartz and fluorite, and finally calcite with intercalated opal forming the bulk of the coatings) indicate progressive changes in UZ conditions through time, rather than repeated saturation by flooding. Percolation under the influence of gravity also results in mineral textures that vary between steeply dipping sites (thinner coatings of blocky calcite) and shallowly dipping sites (thicker coatings of coarse, commonly bladed calcite, with globules and sheets of opal). Micrometer-scale growth banding in both calcite and opal reflects slow average growth rates (scale of mm/m.y.) over millions of years rather than only a few rapidly deposited growth episodes. Isotopic compositions of C, O, Sr, and U from calcite and opal indicate a percolation-modified meteoric water source, and collectively refute a deeper ground-water source. Chemical and isotopic variations in coatings also indicate long-term evolution of water compositions. Although some compositional changes are related to shifts in climate, growth rates in the deeper UZ are buffered from large changes in meteoric input. Coatings most likely formed from films of water flowing down connected fracture pathways. Mineral precipitation is consistent with water vapor and carbon dioxide loss from films at very slow rates. Data collectively indicate that mineral coatings

Presence of sulfate does not inhibit low-temperature dolomite precipitation

NARCIS (Netherlands)

Sánchez-Román, Mónica; McKenzie, Judith A.; de Luca Rebello Wagener, Angela; Rivadeneyra, Maria A.; Vasconcelos, Crisógono

2009-01-01

The hypothesis that sulfate inhibits dolomite formation evolved from geochemical studies of porewaters from deep-sea sedimentary sequences and has been tested with hydrothermal experiments. We examined the sulfate inhibition factor using aerobic culture experiments with Virgibacillus marismortui and

Synthesis of sub-millimeter calcite from aqueous solution

Science.gov (United States)

Reimi, M. A.; Morrison, J. M.; Burns, P. C.

2011-12-01

A novel aqueous synthesis that leads to the formation of calcite (CaCO3) crystals, up to 500μm in diameter, will be used to facilitate the study of contaminant transport in aqueous environmental systems. Existing processes tend to be complicated and often yield nanometer-sized or amorphous CaCO3. The synthesis method presented here, which involves slow mixing of concentrated solutions of CaCl2 ¬and (NH4)2CO3, produces single crystals of rhombohedral calcite in 2 to 4 days. Variations on the experimental method, including changes in pH and solution concentration, were explored to optimize the synthesis. Scanning Electron Microscope images show the differences in size and purity observed when the crystals are grown at pH values ranging from 2 to 6. The crystals grown from solutions of pH 2 were large (up to 500 micrometers in diameter) with minimal polycrystalline calcium carbonate, while crystals grown from solutions with pH values beyond 4 were smaller (up to 100 micrometers in diameter) with significant polycrystalline calcium carbonate. The synthesis method, materials characterization, and use in future actinide contaminant studies will be discussed.

Diagenetic alteration in low-Mg calcite from macrofossils

DEFF Research Database (Denmark)

Ullmann, Clemens Vinzenz; Korte, Christoph

2015-01-01

microscopy) and chemical (trace element abundances, isotopic ratios) screening techniques used to assess the alteration degree of low-Mg calcite macrofossils and summarize the findings on diagenetic trends observed for elemental and isotopic systems in such materials. For a robust evaluation...... of the preservation state of biogenic calcite, it is advisable to combine a set of complementary techniques. Absolute limiting values of element and isotope ratios for discarding diagenetically altered materials cannot be universally applied, but should rather be evaluated on a case to case basis. The evaluation can...

Space-time evolution of cataclasis in carbonate fault zones

Science.gov (United States)

Ferraro, Francesco; Grieco, Donato Stefano; Agosta, Fabrizio; Prosser, Giacomo

2018-05-01

The present contribution focuses on the micro-mechanisms associated to cataclasis of both calcite- and dolomite-rich fault rocks. This work combines field and laboratory data of carbonate fault cores currently exposed in central and southern Italy. By first deciphering the main fault rock textures, their spatial distribution, crosscutting relationships and multi-scale dimensional properties, the relative timing of Intragranular Extensional Fracturing (IEF), chipping, and localized shear is inferred. IEF was predominant within already fractured carbonates, forming coarse and angular rock fragments, and likely lasted for a longer period within the dolomitic fault rocks. Chipping occurred in both lithologies, and was activated by grain rolling forming minute, sub-rounded survivor grains embedded in a powder-like carbonate matrix. The largest fault zones, which crosscut either limestones or dolostones, were subjected to localized shear and, eventually, to flash temperature increase which caused thermal decomposition of calcite within narrow (cm-thick) slip zones. Results are organized in a synoptic panel including the main dimensional properties of survivor grains. Finally, a conceptual model of the time-dependent evolution of cataclastic deformation in carbonate rocks is proposed.

Interactions between cadmium and calcite

NARCIS (Netherlands)

van der Weijden, R.D.

1995-01-01

The thesis is composed of five chapters, some of which have been published or have been accepted for publication. The contents in some of the chapters may therefore slightly overlap, also because the subjects are closely related. The first two chapters focus mostly on the sorption of Cd on calcite,

Morphological changes of calcite single crystals induced by graphene-biomolecule adducts

Science.gov (United States)

Calvaresi, Matteo; Di Giosia, Matteo; Ianiro, Alessandro; Valle, Francesco; Fermani, Simona; Polishchuk, Iryna; Pokroy, Boaz; Falini, Giuseppe

2017-01-01

Calcite has the capability to interact with a wide variety of molecules. This usually induces changes in shape and morphology of crystals. Here, this process was investigated using sheets of graphene-biomolecule adducts. They were prepared and made dispersible in water through the exfoliation of graphite by tip sonication in the presence tryptophan or N-acetyl-D-glucosamine. The crystallization of calcium carbonate in the presence of these additives was obtained by the vapor diffusion method and only calcite formed. The analysis of the microscopic observations showed that the graphene-biomolecule adducts affected shape and morphology of rhombohedral {10.4} faced calcite crystals, due to their stabilization of additional {hk.0} faces. The only presence of the biomolecule affected minimally shape and morphology of calcite crystals, highlighting the key role of the graphene sheets as 2D support for the adsorption of the biomolecules.

Calcite Fluid Inclusion, Paragenetic, and Oxygen Isotopic Records of Thermal Event(s) at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Peterman, B.; Moscati, R.

2000-01-01

Yucca Mountain, Nevada, is under consideration as a potential high-level radioactive waste repository situated above the water table in 12.7 Ma tuffs. A wealth of textural and geochemical evidence from low-temperature deposits of calcite and silica, indicates that their genesis is related to unsaturated zone (UZ) percolation and that the level of the potential repository has never been saturated. Nonetheless, some scientists contend that thermal waters have periodically risen to the surface depositing calcite and opal in the tuffs and at the surface. This hypothesis received some support in 1996 when two-phase fluid inclusions (FIs) with homogenization temperatures (Th) between 35 and 75 C were reported from UZ calcite. Calcite deposition likely followed closely on the cooling of the tuffs and continues into the present. The paragenetic sequence of calcite and silica in the UZ is early stage calcite followed by chalcedony and quartz, then calcite with local opal during middle and late stages. Four types of FIs are found in calcite assemblages: (1) all-liquid (L); (2) all-vapor (V); (3) 2-phase with large and variable V:L ratios; and (4) a few 2-phase with small and consistent V:L ratios. Late calcite contains no FI assemblages indicating elevated depositional temperatures. In early calcite, the Th of type 4 FIs ranges from ∼ 40 to ∼ 85 C. Such temperatures (sub-boiling) and the assemblage of FIs are consistent with deposition in the UZ. Some delta 18O values < 10 permil in early calcite support such temperatures. Type 4 FIs, however, seem to be restricted to the early calcite stage, during which either cooling of the tuffs or regional volcanism were possible heat sources. Nonetheless, at present there is no compelling evidence of upwelling water as a source for the calcite/opal deposits

Sea urchin tooth mineralization: calcite present early in the aboral plumula.

Science.gov (United States)

Stock, Stuart R; Veis, Arthur; Xiao, Xianghui; Almer, Jonathan D; Dorvee, Jason R

2012-11-01

In both vertebrate bone, containing carbonated hydroxyapatite as the mineral phase, and in invertebrate hard tissue comprised of calcium carbonate, a popular view is that the mineral phase develops from a long-lived amorphous precursor which later transforms into crystal form. Important questions linked to this popular view are: when and where is the crystallized material formed, and is amorphous solid added subsequently to the crystalline substrate? Sea urchin teeth, in which the earliest mineral forms within isolated compartments, in a time and position dependent manner, allow direct investigation of the timing of crystallization of the calcite primary plates. Living teeth of the sea urchin Lytechinus variegatus, in their native coelomic fluid, were examined by high-energy synchrotron X-ray diffraction. The diffraction data show that calcite is present in the most aboral portions of the plumula, representing the very earliest stages of mineralization, and that this calcite has the same crystal orientation as in the more mature adoral portions of the same tooth. Raman spectroscopy of the aboral plumula confirms the initial primary plate mineral material is calcite and does not detect amorphous calcium carbonate; in the more mature adoral incisal flange, it does detect a broader calcite peak, consistent with two or more magnesium compositions. We hypothesize that some portion of each syncytial membrane in the plumula provides the information for nucleation of identically oriented calcite crystals that subsequently develop to form the complex geometry of the single crystal sea urchin tooth. Copyright © 2012 Elsevier Inc. All rights reserved.

Sequestration of Antimony on Calcite Observed by Time-Resolved Nanoscale Imaging.

Science.gov (United States)

Renard, François; Putnis, Christine V; Montes-Hernandez, German; King, Helen E; Breedveld, Gijs D; Okkenhaug, Gudny

2018-01-02

Antimony, which has damaging effects on the human body and the ecosystem, can be released into soils, ground-, and surface waters either from ore minerals that weather in near surface environments, or due to anthropogenic releases from waste rich in antimony, a component used in batteries, electronics, ammunitions, plastics, and many other industrial applications. Here, we show that dissolved Sb can interact with calcite, a widespread carbonate mineral, through a coupled dissolution-precipitation mechanism. The process is imaged in situ, at room temperature, at the nanometer scale by using an atomic force microscope equipped with a flow-through cell. Time-resolved imaging allowed following the coupled process of calcite dissolution, nucleation of precipitates at the calcite surface and growth of these precipitates. Sb(V) forms a precipitate, whereas Sb(III) needs to be oxidized to Sb(V) before being incorporated in the new phase. Scanning-electron microscopy and Raman spectroscopy allowed identification of the precipitates as two different calcium-antimony phases (Ca 2 Sb 2 O 7 ). This coupled dissolution-precipitation process that occurs in a boundary layer at the calcite surface can sequester Sb as a solid phase on calcite, which has environmental implications as it may reduce the mobility of this hazardous compound in soils and groundwaters.

Interaction of alcohols with the calcite surface

DEFF Research Database (Denmark)

Bovet, Nicolas Emile; Yang, Mingjun; Javadi, Meshkat Sadat

2015-01-01

. Controlling their growth requires complex polysaccharides. Polysaccharide activity depends on the functionality of OH groups, so to simplify the system in order to get closer to a molecular level understanding, we investigated the interaction of OH from a suite of alcohols with clean, freshly cleaved calcite...... surfaces. X-ray photoelectron spectroscopy (XPS) provided binding energies and revealed the extent of surface coverage. Molecular dynamics (MD) simulations supplemented with information about molecule ordering, orientation and packing density. The results show that all alcohols studied bond...... with the calcite surface through the OH group, with their carbon chains sticking away in a standing-up orientation. Alcohol molecules are closely packed and form a well-ordered monolayer on the surface....

Integrated Approach for Understanding Impurity Adsorption on Calcite: Mechanisms for Micro-scale Surface Phenomena

Science.gov (United States)

Vinson, M. D.; Arvidson, R. S.; Luttge, A.

2004-12-01

A longstanding goal within the field of environmental geochemistry has been the development of a fundamental understanding of the kinetics that governs the interactions of solution-borne impurities with the calcite mineral surface. Recent dissolution experiments using Mg2+, Mn2+, and Sr2+ have shown distinct differences in the interaction of these three impurity ions with the calcite crystal surface. Because the dissolution of carbonate minerals in soils and sediments influences the uptake and migration of groundwater contaminants, a rigorous understanding of the basic processes that occur at the mineral-fluid interface is necessary. We have used vertical scanning interferometry (VSI) coupled with scanning probe microscopy (SPM) to examine calcite crystal dissolution in the presence of Mg2+, Mn2+, and Sr2+, all known dissolution inhibitors and possible groundwater contaminants. We have studied the kinetics of impurity-crystal interactions at a pH 8.8, and in the presence or absence of dissolved inorganic carbon. Our data show that, when individually introduced into undersaturated solutions, Mg2+ and Mn2+ are shown to activate the calcite crystal surface, resulting in enhanced etch pit nucleation rates and step density. Conversely, Sr2+ is shown to cause passivation of the calcite surface. The effect is intensified when solutions are saturated with respect to atmospheric CO2. Results indicate that aqueous CO32- (or HCO3-) may influence how aqueous metal ionic complexes interact with the crystal surface. Furthermore, the influence is differently exhibited, and passivation or activation ultimately depends on the properties of the diffusing metal ion or metal-hydroxide complex. These properties include for example, differences in hydration enthalpy, the effective ionic radius, and electron shell configuration.

Distribution of Minor Elements in Calcite From the Unsaturated Zone at Yucca Mountain, Nevada

Science.gov (United States)

Marshall, B. D.; Whelan, J. F.

2001-12-01

Calcite is sporadically distributed in fractures and cavities in the volcanic rocks that form the 500- to 700-m-thick unsaturated zone at Yucca Mountain. Previous work has shown that the calcite precipitated from water moving downward through the unsaturated zone since the volcanic rocks were emplaced approximately 13 Ma. Calcite thus serves as a proxy for the chemistry and amounts of past percolation, two parameters that are important in predictions of the future behavior of the potential radioactive waste repository at Yucca Mountain. Latest calcite, which began forming between approximately 5 and 2 Ma, typically displays fine-scale growth zoning defined by distributions of Mn (inferred from cathodoluminescence), Mg, and Sr. Electron microprobe (EPMA) mapping of outermost calcite reveals Mg growth zoning1 and higher overall concentrations of Mg in late calcite than in older calcite. Micro X-ray fluorescence (micro-XRF) maps were obtained by slow rastering of the samples over a 100-watt X-ray source collimated through a final aperture of 100 μ m. Although the spatial resolution of the micro-XRF mapping is much less than that of EPMA, this technique reveals distributions of some elements to which EPMA is less sensitive. Micro-XRF maps show that Sr is spatially correlated with Mg; Sr concentrations range to 500 μ g/g at the resolution of the 100-μ m collimator. Because both Mg and Sr have similar calcite-water distribution coefficients much less than one, the Mg/Sr in calcite reflects the Mg/Sr of the water that precipitated the calcite. The distribution coefficient for Mn is greater than one and variations in Mn are not correlated with Mg and Sr. Covariation of Mg and Sr in the percolating water may be explained by reactions that affect the rate of uptake of chemical constituents from the overlying rock and soil, and/or evaporation. Late calcite has lower δ 13C values, probably due to a regional change from wetter to drier climate conditions. The higher Mg and

Mineralogical, crystallographic, and isotopic constraints on the precipitation of aragonite and calcite at Shiqiang and other hot springs in Yunnan Province, China

Science.gov (United States)

Jones, Brian; Peng, Xiaotong

2016-11-01

Two active spring vent pools at Shiqiang (Yunnan Province, China) are characterized by a complex array of precipitates that coat the wall around the pool and the narrow ledges that surround the vent pool. These precipitates include arrays of aragonite crystals, calcite cone-dendrites, red spar calcite, unattached dodecahedral and rhombohedral calcite crystals, and late stage calcite that commonly coats and disguises the earlier formed precipitates. Some of the microbial mats that grow on the ledges around the pools have been partly mineralized by microspheres that are formed of Si and minor amounts of Fe. The calcite and aragonite that are interspersed with each other at all scales are both primary precipitates. Some laminae, for example, change laterally from aragonite to calcite over distances of only a few millimetres. The precipitates at Shiqiang are similar to precipitates found in and around the vent pools of other springs found in Yunnan Province, including those at Gongxiaoshe, Zhuyuan, Eryuan, and Jifei. In all cases, the δDwater and δ18Owater indicate that the spring water is of meteoric origin. These are thermogene springs with the carrier CO2 being derived largely from the mantle and reaction of the waters with bedrock. Variations in the δ13Ctravertine values indicate that the waters in these springs were mixed, to varying degrees, with cold groundwater and its soil-derived CO2. Calcite and aragonite precipitation took place once the spring waters had become supersaturated with respect to CaCO3, probably as a result of rapid CO2 degassing. These precipitates, which were not in isotopic equilibrium with the spring water, are characterized by their unusual crystal morphologies. The precipitation of calcite and aragonite, seemingly together, can probably be attributed to microscale variations in the saturation levels that are, in turn, attributable to microscale variations in the rate of CO2 degassing.

Evaluation of dolomitic resources of Uruguay (Minas - Pan de Azucar Region)

International Nuclear Information System (INIS)

Arrighetti, R; Pirelli, H.; Gianotti, V.; humberto.pirelli@dinamige.miem.gub.uy

2007-01-01

This investigation tries - through Phase I and Phase II stages - to get and estimation of the volume of dolomite resources by means of prospecting the region between the city of Minas and the Pan de Azucar hill, Uruguay; with the objective of achieve a reactivation of this area, increasing job offer, commerce, industrial production and construction activities. Phase I is intended to add valuable information about the precise location of calcareous bodies, their basic features, its geochemical characterization and definition of bodies to be studied with higher detail in Phase II. This second stage points to get an evaluation of the Inferred Resources using 1:10 000 maps and lithological sampling networks to obtain a geochemical characterization of the rocky bodies and the core samples extracted by drilling.Keywords: dolomite, exploration, evaluation, Uruguay. (author)

Gallium isotope fractionation during Ga adsorption on calcite and goethite

Science.gov (United States)

Yuan, Wei; Saldi, Giuseppe D.; Chen, JiuBin; Vetuschi Zuccolini, Marino; Birck, Jean-Louis; Liu, Yujie; Schott, Jacques

2018-02-01

Gallium (Ga) isotopic fractionation during its adsorption on calcite and goethite was investigated at 20 °C as a function of the solution pH, Ga aqueous concentration and speciation, and the solid to solution ratio. In all experiments Ga was found to be enriched in light isotopes at the solid surface with isotope fractionation △71Gasolid-solution up to -1.27‰ and -0.89‰ for calcite and goethite, respectively. Comparison of Ga isotopic data of this study with predictions for 'closed system' equilibrium and 'Rayleigh fractionation' models indicates that the experimental data are consistent with a 'closed system' equilibrium exchange between the fluid and the solid. The results of this study can be interpreted based on Ga aqueous speciation and the structure of Ga complexes formed at the solid surfaces. For calcite, Ga isotope fractionation is mainly triggered by increased Ga coordination and Ga-O bond length, which vary respectively from 4 and 1.84 Å in Ga(OH)4- to 6 and 1.94 Å in the >Ca-O-GaOH(OH2)4+ surface complex. For goethite, despite the formation of Ga hexa-coordinated >FeOGa(OH)20 surface complexes (Ga-O distances of 1.96-1.98 Å) both at acid and alkaline pH, a similar extent of isotope fractionation was found at acid and alkaline pH, suggesting that Ga(OH)4- is preferentially adsorbed on goethite for all investigated pH conditions. In addition, the observed decrease of Ga isotope fractionation magnitude observed with increasing Ga surface coverage for both calcite and goethite is likely related to the formation of Ga surface polymers and/or hydroxides with reduced Ga-O distances. This first study of Ga isotope fractionation during solid-fluid interactions suggests that the adsorption of Ga by oxides, carbonates or clay minerals could yield significant Ga isotope fractionation between secondary minerals and surficial fluids including seawater. Ga isotopes thus should help to better characterize the surficial biogeochemical cycles of gallium and its

Reconstruction of the pre-compactional thickness of the Zechstein Main Dolomite in northwest Poland

Directory of Open Access Journals (Sweden)

Semyrka Grażyna

2015-12-01

Full Text Available Our reconstruction of the pre-compactional thickness of the Main Dolomite strata from the so-called Grotów Peninsula (northwest Poland was based on macroscopic observations of drill cores from three wells: Mokrzec-1, Sieraków-4 and Międzychód-5. These wells are located in various palaeogeographical zones of the Main Dolomite and cored rocks represent a range of microfacies. The amount of compactional reduction in thickness of the Main Dolomite was estimated by summing the total heights (Wst of all stylolites encountered in logs of these wells. For calculations, a generalised model of a drill core was developed, which embraced all types of stylolite seams present in the Main Dolomite succession studied. Also the method of stylolite dimensioning was demonstrated. The number of stylolites in the drill cores studied varied from 511 in the Sieraków-4 well to 1,534 in the Międzychód-5 well. In all cores studied low-amplitude macrostylolites predominated, but the reduction of thickness was controlled mostly by the low- and medium-amplitude macrostylolites. The largest number of stylolites was found in the grainstone/packstone microfacies. The turnout of stylolites depends of microfacies. The highest density of stylolites was documented in mudstones/wackestones (24 stylolites per metre of rock thickness and the lowest in boundstones (14 stylolites per metre of rock thickness. The low-amplitude stylolites appear most frequently in the mudstone/wackestone microfacies (15 stylolites per metre of rock thickness; in grainstones/packstones, rudstones/floatstones and boundstones middle-amplitude stylolites are rare (3 stylolites per metre of rock thickness. The degree of compaction of the Main Dolomite succession studied varied from 6 to 10%; hence, its calculated initial thickness also varied in the wells studied: from 41.3 m in the Sieraków-4 well to 56.9 m in the Mokrzec-1 well and to 97.1 m in the Międzychód-5 well. The volumes of reservoir

Calcite Formation in Soft Coral Sclerites Is Determined by a Single Reactive Extracellular Protein*

Science.gov (United States)

Rahman, M. Azizur; Oomori, Tamotsu; Wörheide, Gert

2011-01-01

Calcium carbonate exists in two main forms, calcite and aragonite, in the skeletons of marine organisms. The primary mineralogy of marine carbonates has changed over the history of the earth depending on the magnesium/calcium ratio in seawater during the periods of the so-called “calcite and aragonite seas.” Organisms that prefer certain mineralogy appear to flourish when their preferred mineralogy is favored by seawater chemistry. However, this rule is not without exceptions. For example, some octocorals produce calcite despite living in an aragonite sea. Here, we address the unresolved question of how organisms such as soft corals are able to form calcitic skeletal elements in an aragonite sea. We show that an extracellular protein called ECMP-67 isolated from soft coral sclerites induces calcite formation in vitro even when the composition of the calcifying solution favors aragonite precipitation. Structural details of both the surface and the interior of single crystals generated upon interaction with ECMP-67 were analyzed with an apertureless-type near-field IR microscope with high spatial resolution. The results show that this protein is the main determining factor for driving the production of calcite instead of aragonite in the biocalcification process and that –OH, secondary structures (e.g. α-helices and amides), and other necessary chemical groups are distributed over the center of the calcite crystals. Using an atomic force microscope, we also explored how this extracellular protein significantly affects the molecular-scale kinetics of crystal formation. We anticipate that a more thorough investigation of the proteinaceous skeleton content of different calcite-producing marine organisms will reveal similar components that determine the mineralogy of the organisms. These findings have significant implications for future models of the crystal structure of calcite in nature. PMID:21768106

Role of Mg{sub x}Ca{sub 1−x}CO{sub 3} on the physical–chemical properties and cyclic CO{sub 2} capture performance of dolomite by two-step calcination

Energy Technology Data Exchange (ETDEWEB)

Wang, Ke; Han, Dongtai, E-mail: handongtai@cumt.edu.cn; Zhao, Pengfei, E-mail: zhaopfcumt@163.com; Hu, Xiumeng; Yin, Zeguang; Wu, Di

2015-08-20

Highlights: • Two-step calcination treated dolomite sorbent was prepared and characterized. • An intermediate phase (Mg{sub x}Ca{sub 1−x}CO{sub 3}) was observed by TG and XRD results. • Mg-calcite hindered the de-mixing of Ca and Mg. • Smaller grains, larger specific surface area and pore volume were obtained. • This favorable structure resulted in a high and stable CO{sub 2} capture performance. - Abstract: Two-step calcination (CO{sub 2} and N{sub 2} atmospheres) was used to modify the microstructure of natural dolomite for high-temperature CO{sub 2} capture. Two other one-step calcinations (CO{sub 2} or N{sub 2} atmosphere) were provided for comparison. Different morphological characterizations (thermal decomposition, phase composition, morphology, and nitrogen adsorption) were performed, followed by an analysis of 30 carbonation/calcination cycles in a fixed bed reactor. During primary calcination in a CO{sub 2} atmosphere, an intermediate phase (Mg{sub x}Ca{sub 1−x}CO{sub 3}) was observed by TG and XRD results, which hindered the de-mixing of CaO and MgO in the secondary calcination in a N{sub 2} atmosphere. Therefore, two-step calcination produced smaller grains (CaO: 45.2 nm; MgO: 32.6 nm), larger specific surface area (21.08 m{sup 2}/g) and pore volume (0.082 cm{sup 3}/g) and uniform distribution of CaO and MgO, which resulted in a higher and more stable uptake of CO{sub 2} compared to the results from one-step calcinations.

Quantifying Rock Weakening Due to Decreasing Calcite Mineral Content by Numerical Simulations.

Science.gov (United States)

Wetzel, Maria; Kempka, Thomas; Kühn, Michael

2018-04-01

The quantification of changes in geomechanical properties due to chemical reactions is of paramount importance for geological subsurface utilisation, since mineral dissolution generally reduces rock stiffness. In the present study, the effective elastic moduli of two digital rock samples, the Fontainebleau and Bentheim sandstones, are numerically determined based on micro-CT images. Reduction in rock stiffness due to the dissolution of 10% calcite cement by volume out of the pore network is quantified for three synthetic spatial calcite distributions (coating, partial filling and random) using representative sub-cubes derived from the digital rock samples. Due to the reduced calcite content, bulk and shear moduli decrease by 34% and 38% in maximum, respectively. Total porosity is clearly the dominant parameter, while spatial calcite distribution has a minor impact, except for a randomly chosen cement distribution within the pore network. Moreover, applying an initial stiffness reduced by 47% for the calcite cement results only in a slightly weaker mechanical behaviour. Using the quantitative approach introduced here substantially improves the accuracy of predictions in elastic rock properties compared to general analytical methods, and further enables quantification of uncertainties related to spatial variations in porosity and mineral distribution.

The Mississippian Leadville Limestone Exploration Play, Utah and Colorado-Exploration Techniques and Studies for Independents

Energy Technology Data Exchange (ETDEWEB)

Thomas Chidsey

2008-09-30

-marine facies constitute a significant reservoir potential, having both effective porosity and permeability when dissolution of skeletal grains, followed by dolomitization, has occurred. Two major types of diagenetic dolomite are observed in the Leadville Limestone at Lisbon field: (1) tight 'early' dolomite consisting of very fine grained (<5 {micro}m), interlocking crystals that faithfully preserve depositional fabrics; and (2) porous, coarser (>100-250 {micro}m), rhombic and saddle crystals that discordantly replace limestone and earlier very fine grained dolomite. Predating or concomitant with late dolomite formation are pervasive leaching episodes that produced vugs and extensive microporosity. Most reservoir rocks within Lisbon field appear to be associated with the second, late type of dolomitization and associated leaching events. Other diagenetic products include pyrobitumen, syntaxial cement, sulfide minerals, anhydrite cement and replacement, and late macrocalcite. Fracturing (solution enlarged) and brecciation (autobrecciation) caused by hydrofracturing are widespread within Lisbon field. Sediment-filled cavities, related to karstification of the exposed Leadville, are present in the upper third of the formation. Pyrobitumen and sulfide minerals appear to coat most crystal faces of the rhombic and saddle dolomites. The fluid inclusion and mineral relationships suggest the following sequence of events: (1) dolomite precipitation, (2) anhydrite deposition, (3) anhydrite dissolution and quartz precipitation, (4) dolomite dissolution and late calcite precipitation, (5) trapping of a mobile oil phase, and (6) formation of bitumen. Fluid inclusions in calcite and dolomite display variable liquid to vapor ratios suggesting reequilibration at elevated temperatures (50 C). Fluid salinities exceed 10 weight percent NaCl equivalent. Low ice melting temperatures of quartz- and calcite-hosted inclusions suggest chemically complex Ca-Mg-bearing brines associated with

The Mississippian Leadville Limestone Exploration Play, Utah and Colorado-Exploration Techniques and Studies for Independents

International Nuclear Information System (INIS)

Thomas Chidsey

2008-01-01

-marine facies constitute a significant reservoir potential, having both effective porosity and permeability when dissolution of skeletal grains, followed by dolomitization, has occurred. Two major types of diagenetic dolomite are observed in the Leadville Limestone at Lisbon field: (1) tight 'early' dolomite consisting of very fine grained ( 100-250 (micro)m), rhombic and saddle crystals that discordantly replace limestone and earlier very fine grained dolomite. Predating or concomitant with late dolomite formation are pervasive leaching episodes that produced vugs and extensive microporosity. Most reservoir rocks within Lisbon field appear to be associated with the second, late type of dolomitization and associated leaching events. Other diagenetic products include pyrobitumen, syntaxial cement, sulfide minerals, anhydrite cement and replacement, and late macrocalcite. Fracturing (solution enlarged) and brecciation (autobrecciation) caused by hydrofracturing are widespread within Lisbon field. Sediment-filled cavities, related to karstification of the exposed Leadville, are present in the upper third of the formation. Pyrobitumen and sulfide minerals appear to coat most crystal faces of the rhombic and saddle dolomites. The fluid inclusion and mineral relationships suggest the following sequence of events: (1) dolomite precipitation, (2) anhydrite deposition, (3) anhydrite dissolution and quartz precipitation, (4) dolomite dissolution and late calcite precipitation, (5) trapping of a mobile oil phase, and (6) formation of bitumen. Fluid inclusions in calcite and dolomite display variable liquid to vapor ratios suggesting reequilibration at elevated temperatures (50 C). Fluid salinities exceed 10 weight percent NaCl equivalent. Low ice melting temperatures of quartz- and calcite-hosted inclusions suggest chemically complex Ca-Mg-bearing brines associated with evaporite deposits were responsible for mineral deposition. The overall conclusion from these analyses indicates late

Paleohydrogeological implications from fracture calcites and sulfides in a major hydrogeological zone HZ19 at Olkiluoto

International Nuclear Information System (INIS)

Sahlstedt, E.; Karhu, J.; Rinne, K.

2009-08-01

30 samples of fracture mineral fillings in or near water conducting fractures at Olkiluoto were collected from 10 drill cores for fracture mineral studies. The aim of the study was to obtain information about past hydrogeochemical conditions at Olkiluoto using the calcite morphology, the chemical characteristics and the isotopic composition of carbon and oxygen in calcite. The chemical composition of fracture calcites at Olkiluoto is nearly stoichiometric CaCO 3 . Most variation in the composition of calcite is due to differences in the Mn content, which could indicate variations in groundwater redox conditions. Meaningful REE patterns were obtained for the calcites. REE patterns showed generally negative Eu anomalies, but one fracture calcite specimen had a distinct positive Eu anomaly. This positive anomaly could be related to ancient hydrothermal conditions, although derivation of the anomaly from the host rock cannot be excluded. Preliminary results for calcite U-Th dating of fracture calcites are reported. The isotopic composition of U and Th were analysed by a new multiple collector LA-ICPMS instrument. U and Th concentrations in fracture calcites are generally 18 O values of calcite range from -17 to -7 per mille. Most of the calcites may have been precipitated in the presence of waters with oxygen isotope ratios similar to those in the present-day groundwaters at Olkiluoto. Two samples with an oxygen isotopic composition highly depleted in 18 O were interpreted to have been precipitated at elevated temperatures. The δ 13 C values of calcite showed a wide range of values from -26 to +35 per mille. Multiple sources for carbon are implied. The highest δ 13 C values indicate methanic conditions in the fracture at the time of calcite precipitation. It appears that the methanic environment has earlier extended to shallower depths compared to the location of the methanic environment in the present-day fracture system (> 300 m). Ten pyrite samples were analysed

Isolation and identification of Pseudomonas azotoformans for induced calcite precipitation.

Science.gov (United States)

Heidari Nonakaran, Siamak; Pazhouhandeh, Maghsoud; Keyvani, Abdullah; Abdollahipour, Fatemeh Zahra; Shirzad, Akbar

2015-12-01

Biomineralization is a process by which living organisms produce minerals. The extracellular production of these biominerals by microbes has potential for various bioengineering applications. For example, crack remediation and improvement of durability of concrete is an important goal for engineers and biomineral-producing microbes could be a useful tool in achieving this goal. Here we report the isolation, biochemical characterization and molecular identification of Pseudomonas azotoformans, a microbe that produces calcite and which potentially be used to repair cracks in concrete structures. Initially, 38 bacterial isolates were isolated from soil and cements. As a first test, the isolates were screened using a urease assay followed by biochemical tests for the rate of urea hydrolysis, calcite production and the insolubility of calcite. Molecular amplification and sequencing of a 16S rRNA fragment of selected isolates permitted us to identify P. azotoformans as a good candidate for preparation of biotechnological concrete. This species was isolated from soil and the results show that among the tested isolates it had the highest rate of urea hydrolysis, produced the highest amount of calcite, which, furthermore was the most adhesive and insoluble. This species is thus of interest as an agent with the potential ability to repair cracks in concrete.

Interactions of Ni and Ca at the calcite-solution interface

International Nuclear Information System (INIS)

Carlsson, T.; Aalto, H.

1996-10-01

The performance assessment of repositories for spent nuclear fuel need, among other things, data describing the solubilities of radionuclides in the near field and far field. The solubility limits are often used in order to estimate the maximum concentrations of radionuclides during their possible transport to the biosphere. The solubilities used are mostly the individual solubilities for pure solids of the actual radionuclides. This way of using solubility limits represents a conservative performance assessment where the estimated nuclide concentrations are unrealistically high. This is acceptable from a performance assessment point of view but very unsatisfactory for an optimal design of the repository. In order to make the assessment more realistic, coprecipitation and solid solution formation should be taken into account. Only solids which are, in geological terms, formed in fast reactions need to be considered, which in practice restricts the number of radionuclide scavengers to calcite and iron(III)oxihydroxide. This work focuses on the Ni coprecipitation with calcite. The systems were studied under anoxic conditions and consisted of calcite-saturated 0.05 M NaCl solutions in equilibrium with synthetic calcite. The solutions were initially spiked with 63 Ni and 45 Ca and the concentrations of these elements were determined using liquid scintillation counting. (18 refs.)

Study of marbles from Middle Atlas (Morocco): elemental, mineralogical and structural analysis

Science.gov (United States)

Khrissi, S.; Bejjit, L.; Haddad, M.; Falguères, C.; Ait Lyazidi, S.; El Amraoui, M.

2018-05-01

A series of marbles sampled from the region of Middle Atlas (Morocco), are characterized by different complementary spectroscopic techniques. X-Ray fluorescence is used to determine elemental composition of rock while X-Ray diffraction and the Raman spectroscopy are used to determine major crystalline phases (calcite and dolomite) and minor ones (quartz).The samples display typical EPR spectra of Mn2+ in calcite and reveal the presence of Fe3+ ions.

Controlling the size and morphology of precipitated calcite particles by the selection of solvent composition

Science.gov (United States)

Konopacka-Łyskawa, Donata; Kościelska, Barbara; Karczewski, Jakub

2017-11-01

Precipitated calcium carbonate is used as an additive in the manufacture of many products. Particles with specific characteristics can be obtained by the selection of precipitation conditions, including temperature and the composition of solvent. In this work, calcium carbonate particles were obtained in the reaction of calcium hydroxide with carbon dioxide at 65 °C. Initial Ca(OH)2 suspensions were prepared in pure water and aqueous solutions of ethylene glycol or glycerol of the concentration range up to 20% (vol.). The course of reaction was monitored by conductivity measurements. Precipitated solids were analyzed by FTIR, XRD, SEM and the particles size distribution was determined by a laser diffraction method. The adsorption of ethylene glycol or glycerol on the surface of scalenohedral and rhombohedral calcite was testes by a normal-phase high-performance liquid chromatography. The addition of organic solvents changed the viscosity of reaction mixtures, the rate of carbon dioxide absorption and the solubility of inorganic components and therefore influence calcium carbonate precipitation conditions. All synthesized calcium carbonate products were in a calcite form. Scalenohedral calcite crystals were produced when water was a liquid phase, whereas addition of organic solvents resulted in the formation of rhombo-scalenohedral particles. The increase in organic compounds concentration resulted in the decrease of mean particles size from 2.4 μm to 1.7 μm in ethylene glycol solutions and to 1.4 μm in glycerol solutions. On the basis of adsorption tests, it was confirm that calcite surface interact stronger with glycerol than ethylene glycol. The interaction between scalenohedral calcite and used organic additives was higher in comparison to the pure rhombohedral form applied as a stationary phase.

Surface tension alteration on calcite, induced by ion substitution

DEFF Research Database (Denmark)

Sakuma, Hiroshi; Andersson, Martin Peter; Bechgaard, Klaus

2014-01-01

The interaction of water and organic molecules with mineral surfaces controls many processes in nature and industry. The thermodynamic property, surface tension, is usually determined from the contact angle between phases, but how does one understand the concept of surface tension at the nanoscale...... preferentially as ion pairs at solution-calcite interfaces. Mg2+ incorporation weakens organic molecule adhesion while strengthening water adsorption so Mg2+ substitution renders calcite more water wet. When Mg2+ replaces 10% of surface Ca2+, the contact angle changes dramatically, by 40 to 70, converting...

Experimental observation of permeability changes in dolomite at CO2 sequestration conditions.

Science.gov (United States)

Tutolo, Benjamin M; Luhmann, Andrew J; Kong, Xiang-Zhao; Saar, Martin O; Seyfried, William E

2014-02-18

Injection of cool CO2 into geothermally warm carbonate reservoirs for storage or geothermal energy production may lower near-well temperature and lead to mass transfer along flow paths leading away from the well. To investigate this process, a dolomite core was subjected to a 650 h, high pressure, CO2 saturated, flow-through experiment. Permeability increased from 10(-15.9) to 10(-15.2) m(2) over the initial 216 h at 21 °C, decreased to 10(-16.2) m(2) over 289 h at 50 °C, largely due to thermally driven CO2 exsolution, and reached a final value of 10(-16.4) m(2) after 145 h at 100 °C due to continued exsolution and the onset of dolomite precipitation. Theoretical calculations show that CO2 exsolution results in a maximum pore space CO2 saturation of 0.5, and steady state relative permeabilities of CO2 and water on the order of 0.0065 and 0.1, respectively. Post-experiment imagery reveals matrix dissolution at low temperatures, and subsequent filling-in of flow passages at elevated temperature. Geochemical calculations indicate that reservoir fluids subjected to a thermal gradient may exsolve and precipitate up to 200 cm(3) CO2 and 1.5 cm(3) dolomite per kg of water, respectively, resulting in substantial porosity and permeability redistribution.

Early Silurian (Llandoverian) Leask Point and Charlton Bay bioherms, Manitoulin Island, Ontario, Canada

Energy Technology Data Exchange (ETDEWEB)

Mielczarek, W.; Copper, P.

1986-08-01

About 300 bioherms are known in the Llandoverian Manitoulin Formation of eastern Manitoulin Island. In the South Bay area, the large Leask Piont bioherm and Charlton Bay patch-reef complex lack a distinct skeletal growth framework. Bioherms consist of mudstone and wackestone, with isolated lenses of bafflestone, boundstone, floatstone. Fossils are scarce, but crinozoans and bryozoans comprise about 90% of the bioclasts. Other fauna include stromatoporoids, corals, brachiopods, gastropods, trilobites, and probable algae (algae are difficult to identify and may have played a significant role). Faunal ratios remained relatively constant during mound growth. Soft substrates with sedimentation rates of a few millimeters per year are suggested by bedding type and morphologic dominance of lamellar and tabular corals and stromatoporoids. An increased sedimentation rate, resulting from shoaling, is indicated by more overturned, broadly conical corals in the upper parts of the mounds. Shoaling may be responsible for cessation of mound growth. Lithoclasts are more common in the upper parts of the mounds. They formed when semiconsolidated muds were disturbed and redeposited during storms. Megarippled interreef surface areas, largely devoid of coral growth, indicate mud instability at Charlton Bay. Lack of suitable stable substrates may have hampered coral development. Dolomitization was postdepositional. The diagenetic sequence occurred in three stages: 1)selective pyritization and silicification, formation of an early muddy dolomite replacing the mud fraction of the dolostone, lithification and formation of rare calcite cement and neomorphic syntaxial rims; 2)clear, coarse dolomite replacing pore-filling calcite cement, syntaxial rims, and unaltered macrofossils, stylolitization, grain-to-grain dissolution; and 3)a late dolomite found mainly as fine rhombs in stylolites, solution seams, and intraskeletal pore space.

Low-temperature aqueous alteration on the CR chondrite parent body: Implications from in situ oxygen-isotope analyses

Science.gov (United States)

Jilly-Rehak, Christine E.; Huss, Gary R.; Nagashima, Kazu; Schrader, Devin L.

2018-02-01

The presence of hydrated minerals in chondrites indicates that water played an important role in the geologic evolution of the early Solar System; however, the process of aqueous alteration is still poorly understood. Renazzo-like carbonaceous (CR) chondrites are particularly well-suited for the study of aqueous alteration. Samples range from being nearly anhydrous to fully altered, essentially representing snapshots of the alteration process through time. We studied oxygen isotopes in secondary-minerals from six CR chondrites of varying hydration states to determine how aqueous fluid conditions (including composition and temperature) evolved on the parent body. Secondary minerals analyzed included calcite, dolomite, and magnetite. The O-isotope composition of calcites ranged from δ18O ≈ 9 to 35‰, dolomites from δ18O ≈ 23 to 27‰, and magnetites from δ18O ≈ -18 to 5‰. Calcite in less-altered samples showed more evidence of fluid evolution compared to heavily altered samples, likely reflecting lower water/rock ratios. Most magnetite plotted on a single trend, with the exception of grains from the extensively hydrated chondrite MIL 090292. The MIL 090292 magnetite diverges from this trend, possibly indicating an anomalous origin for the meteorite. If magnetite and calcite formed in equilibrium, then the relative 18O fractionation between them can be used to extract the temperature of co-precipitation. Isotopic fractionation in Al Rais carbonate-magnetite assemblages revealed low precipitation temperatures (∼60 °C). Assuming that the CR parent body experienced closed-system alteration, a similar exercise for parallel calcite and magnetite O-isotope arrays yields "global" alteration temperatures of ∼55 to 88 °C. These secondary mineral arrays indicate that the O-isotopic composition of the altering fluid evolved upon progressive alteration, beginning near the Al Rais water composition of Δ17O ∼ 1‰ and δ18O ∼ 10‰, and becoming increasingly

Constraints on the depositional age and tectonometamorphic evolution of marbles from the Biharia Nappe System (Apuseni Mountains, Romania

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Reiser Martin Kaspar

2017-04-01

Full Text Available Basement rocks from the Biharia Nappe System in the Apuseni Mountains comprise several dolomite and calcite marble sequences or lenses which experienced deformation and metamorphic overprint during the Alpine orogeny. New Sr, O and C-isotope data in combination with considerations from the lithological sequences indicate Middle to Late Triassic deposition of calcite marbles from the Vulturese-Belioara Series (Biharia Nappe s.str.. Ductile deformation and large-scale folding of the siliciclastic and carbonatic lithologies is attributed to NW-directed nappe stacking during late Early Cretaceous times (D2. The studied marble sequences experienced a metamorphic overprint under lower greenschist- facies conditions (316-370 °C based on calcite - dolomite geothermometry during this tectonic event. Other marble sequences from the Biharia Nappe System (i.e. Vidolm and Baia de Arieș nappes show similarities in the stratigraphic sequence and their isotope signature, together with a comparable structural position close to nappe contact. However, the dataset is not concise enough to allow for a definitive attribution of a Mesozoic origin to other marble sequences than the Vulturese-Belioara Series.

Differential early diagenetic low-Mg calcite cementation and rhythmic hardground development in Campanian-Maastrichtian chalk

DEFF Research Database (Denmark)

Molenaar, Nicolaas; J.J.P., Zijlstra

1997-01-01

and differences in the degree of early diagenesis. Cemented layers and hardgrounds are the result of differential early marine calcite cementation. In these limestones early calcite cementation cannot be explained by the supply of cementing materials from saturated seawater, An alternative model for early marine......The Campanian-Maastrichtian limestones in the south of the Netherlands are well-sorted fine-grained mudstones and silt- to fine sand-sized bioclastic grainstones. These limestones show a distinct lithological cyclicity manifested by fining-upward grain-size cycles with calcite-cemented layers...... calcite cementation is proposed, in which early calcite cementation occurred within the sediment at some distance below the seafloor as a result of organic matter degradation and internal redistribution of bioclastic carbonate. Bacterial organic matter degradation caused dissolution of relatively unstable...

Index of refraction enhancement of calcite particles coated with zinc carbonate

Science.gov (United States)

Lattaud, Kathleen; Vilminot, Serge; Hirlimann, Charles; Parant, Hubert; Schoelkopf, Joachim; Gane, Patrick

2006-10-01

ZnCO 3 coating on calcite particles has been developed in order to enhance the index of refraction of this mineral that is used as a charge in paper, paint and polymer industries. Chemical reaction between calcite particles in an aqueous suspension with zinc chloride promotes the formation of a ZnCO 3 coating consisting of two layers with different interactions with the calcite particle. The refraction index of the resulting composite particles increases with the Zn/Ca ratio. A model allows to evaluate the coating thickness. The value of the scattering S and diffusion K coefficients of sheets coated with the ZnCO 3 coated particles reveal a dependence on the preparation conditions with a 15% increase for the best samples.

The kinetics and mechanisms of amorphous calcium carbonate (ACC) crystallization to calcite, via vaterite.

Science.gov (United States)

Rodriguez-Blanco, Juan Diego; Shaw, Samuel; Benning, Liane G

2011-01-01

The kinetics and mechanisms of nanoparticulate amorphous calcium carbonate (ACC) crystallization to calcite, via vaterite, were studied at a range of environmentally relevant temperatures (7.5-25 °C) using synchrotron-based in situ time-resolved Energy Dispersive X-ray Diffraction (ED-XRD) in conjunction with high-resolution electron microscopy, ex situ X-ray diffraction and infrared spectroscopy. The crystallization process occurs in two stages; firstly, the particles of ACC rapidly dehydrate and crystallize to form individual particles of vaterite; secondly, the vaterite transforms to calcite via a dissolution and reprecipitation mechanism with the reaction rate controlled by the surface area of calcite. The second stage of the reaction is approximately 10 times slower than the first. Activation energies of calcite nucleation and crystallization are 73±10 and 66±2 kJ mol(-1), respectively. A model to calculate the degree of calcite crystallization from ACC at environmentally relevant temperatures (7.5-40 °C) is also presented.

Ikaite pseudomorphs in the Zaire deep-sea fan: An intermediate between calcite and porous calcite

Science.gov (United States)

Jansen, J. H. F.; Woensdregt, C. F.; Kooistra, M. J.; van der Gaast, S. J.

1987-03-01

Translucent brown aggregates of calcium-carbonate crystals have been found in cores from the Zaire deep-sea fan (west equatorial Africa). The aggregates are well preserved but very friable. Upon storage they become yellowish white and cloudy and release water. Chemical, mineralogical (XRD), petrographical, crystal-morphological, and stable-isotope data demonstrate that the crystals have passed through three phases: (1) an authigenic carbonate phase, probably calcium carbonate, which is represented by the external habit of the present crystals; (2) a translucent brown ikaite phase (CaCO3·6H2O), unstable at temperatures above 5 °C; and (3) a phase consisting of calcite microcrystals that are poorly cemented and form a porous mass within the crystal form of the morphologically unchanged first phase. The transformation from the first phase into ikaite was probably a kinetic replacement. The transformation from ikaite into the third phase occurred because of storage at room temperature. The presence of ikaite is indicative of a low-temperature, anaerobic, organic-carbon-rich marine environment. Ikaite is probably the precursor of a great number of porous calcite pseudomorphs, and possibly also of many marine authigenic microcrystalline carbonate nodules.

Biogenic processes in crystalline bedrock fractures indicated by carbon isotope signatures of secondary calcite

International Nuclear Information System (INIS)

Sahlstedt, Elina; Karhu, Juha A.; Pitkänen, Petteri; Whitehouse, Martin

2016-01-01

Variation in 13 C/ 12 C-isotope ratios of fracture filling calcite was analyzed in situ to investigate carbon sources and cycling in fractured bedrock. The study was conducted by separating sections of fracture fillings, and analyzing the 13 C/ 12 C-ratios with secondary ion mass spectrometry (SIMS). Specifically, the study was aimed at fillings where previously published sulfur isotope data indicated the occurrence of bacterial sulfate reduction. The results showed that the δ 13 C values of calcite were highly variable, ranging from −53.8‰ to +31.6‰ (VPDB). The analysis also showed high variations within single fillings of up to 39‰. The analyzed calcite fillings were mostly associated with two calcite groups, of which Group 3 represents possible Paleozoic fluid circulation, based on comparison with similar dated coatings within the Baltic Shield and the succeeding Group 1–2 fillings represent late-stage, low temperature mineralization and are possibly late Paleozoic to Quaternary in age. Both generations were associated with pyrite with δ 34 S values indicative of bacterial sulfate reduction. The δ 13 C values of calcite, however, were indicative of geochemical environments which were distinct for these generations. The δ 13 C values of Group 3 calcite varied from −22.1‰ to +11‰, with a distinct peak at −16‰ to −12‰. Furthermore, there were no observable depth dependent trends in the δ 13 C values of Group 3 calcite. The δ 13 C values of Group 3 calcite were indicative of organic matter degradation and methanogenesis. In contrast to the Group 3 fillings, the δ 13 C values of Group 1–2 calcite were highly variable, ranging from −53.8‰ to +31.6‰ and they showed systematic variation with depth. The near surface environment of <30 m (bsl) was characterized by δ 13 C values indicative of degradation of surface derived organic matter, with δ 13 C values ranging from −30.3‰ to −5.5‰. The intermediate depth of

Microbially induced separation of quartz from calcite using Saccharomyces cerevisiae.

Science.gov (United States)

Padukone, S Usha; Natarajan, K A

2011-11-01

Cells of Saccharomyces cerevisiae and their metabolites were successfully utilized to achieve selective separation of quartz and calcite through microbially induced flotation and flocculation. S. cerevisiae was adapted to calcite and quartz minerals. Adsorption studies and electrokinetic investigations were carried out to understand the changes in the surface chemistry of yeast cells and the minerals after mutual interaction. Possible mechanisms in microbially induced flotation and flocculation are outlined. Copyright © 2011 Elsevier B.V. All rights reserved.

Thermal and Evolved Gas Behavior of Calcite Under Mars Phoenix TEGA Operating Conditions

Science.gov (United States)

Ming, D.W.; Niles, P.B.; Morris, R.V.; Boynton, W.V.; Golden, D.C.; Lauer, H.V.; Sutter, B.

2009-01-01

The Mars Phoenix Scout Mission with its diverse instrument suite successfully examined several soils on the Northern plains of Mars. The Thermal and Evolved Gas Analyzer (TEGA) was employed to detect organic and inorganic materials by coupling a differential scanning calorimeter (DSC) with a magnetic-sector mass spectrometer (MS). Martian soil was heated up to 1000 C in the DSC ovens and evolved gases from mineral decomposition products were examined with the MS. TEGA s DSC has the capability to detect endothermic and exothermic reactions during heating that are characteristic of minerals present in the Martian soil. Initial TEGA results indicated the presence of endothermic peaks with onset temperatures that ranged from 675 C to 750 C with corresponding CO2 release. This result suggests the presence of calcite (CaCO3. CaO + CO2). Organic combustion to CO2 is not likely since this mostly occurs at temperatures below 550 C. Fe-carbonate and Mg-carbonate are not likely because their decomposition temperatures are less than 600 C. TEGA enthalpy determinations suggest that calcite, may occur in the Martian soil in concentrations of approx.1 to 5 wt. %. The detection of calcite could be questioned based on previous results that suggest Mars soils are mostly acidic. However, the Phoenix landing site soil pH was measured at pH 8.3 0.5, which is typical of terrestrial soils where pH is controlled by calcite solubility. The range of onset temperatures and calcite concentration as calculated by TEGA is poorly con-strained in part because of limited thermal data of cal-cite at reduced pressures. TEGA operates at calcite literature thermal data was obtained at 1000 mbar or higher pressures.

Sorption of phosphate onto calcite; results from batch experiments and surface complexation modeling

DEFF Research Database (Denmark)

Sø, Helle Ugilt; Postma, Dieke; Jakobsen, Rasmus

2011-01-01

The adsorption of phosphate onto calcite was studied in a series of batch experiments. To avoid the precipitation of phosphate-containing minerals the experiments were conducted using a short reaction time (3h) and low concentrations of phosphate (⩽50μM). Sorption of phosphate on calcite was stud......The adsorption of phosphate onto calcite was studied in a series of batch experiments. To avoid the precipitation of phosphate-containing minerals the experiments were conducted using a short reaction time (3h) and low concentrations of phosphate (⩽50μM). Sorption of phosphate on calcite...... of a high degree of super-saturation with respect to hydroxyapatite (SIHAP⩽7.83). The amount of phosphate adsorbed varied with the solution composition, in particular, adsorption increases as the CO32- activity decreases (at constant pH) and as pH increases (at constant CO32- activity). The primary effect...... of ionic strength on phosphate sorption onto calcite is its influence on the activity of the different aqueous phosphate species. The experimental results were modeled satisfactorily using the constant capacitance model with >CaPO4Ca0 and either >CaHPO4Ca+ or >CaHPO4- as the adsorbed surface species...

Selective adsorption of benzhydroxamic acid on fluorite rendering selective separation of fluorite/calcite

Science.gov (United States)

Jiang, Wei; Gao, Zhiyong; Khoso, Sultan Ahmed; Gao, Jiande; Sun, Wei; Pu, Wei; Hu, Yuehua

2018-03-01

Fluorite, a chief source of fluorine in the nature, usually coexists with calcite mineral in ore deposits. Worldwide, flotation techniques with a selective collector and/or a selective depressant are commonly preferred for the separation of fluorite from calcite. In the present study, an attempt was made to use benzhydroxamic acid (BHA) as a collector for the selective separation of fluorite from calcite without using any depressant. Results obtained from the flotation experiments for single mineral and mixed binary minerals revealed that the BHA has a good selective collecting ability for the fluorite when 50 mg/L of BHA was used at pH of 9. The results from the zeta potential and X-ray photoelectron spectroscopy (XPS) indicated that the BHA easily chemisorbs onto the fluorite as compared to calcite. Crystal chemistry calculations showed the larger Ca density and the higher Ca activity on fluorite surface mainly account for the selective adsorption of BHA on fluorite, leading to the selective separation of fluorite from calcite. Moreover, a stronger hydrogen bonding with BHA and the weaker electrostatic repulsion with BHA- also contribute to the stronger interaction of BHA species with fluorite surface.

Environmental controls for the precipitation of different fibrous calcite cement fabrics

Science.gov (United States)

Ritter, Ann-Christine; Wiethoff, Felix; Neuser, Rolf D.; Richter, Detlev K.; Immenhauser, Adrian

2016-04-01

Abiogenic calcite cements are widely used as climate archives. They can yield information on environmental change and climate dynamics at the time when the sediment was lithified in a (marine) diagenetic environment. Radiaxial-fibrous (RFC) and fascicular-optic fibrous (FOFC) calcite cements are two very common and similar pore-filling cement fabrics in Palaeozoic and Mesozoic carbonate rocks (Richter et al., 2011) and in Holocene Mg-calcitic speleothems (Richter et al., 2015). Both fabrics are characterised by distinct crystallographic properties. Current research has shown that these fabrics are often underexplored and that a careful combination of conservative and innovative proxies allows for a better applicability of these carbonate archives to paleoenvironmental reconstructions (Ritter et al., 2015). A main uncertainty in this context is that it is still poorly understood which parameters lead to the formation of either RFC or FOFC and if differential crystallographic parameters affect proxy data from these fabrics. This study aims at a better understanding of the environmental factors that may control either RFC or FOFC precipitation. Therefore, suitable samples (a stalagmite and a Triassic marine cement succession), each with clearly differentiable layers of RFC and FOFC, were identified and analysed in high detail using a multi-proxy approach. Detailed thin section and cathodoluminescence analysis of the samples allowed for a precise identification of layers consisting solely of either RFC or FOFC. Isotopic (δ13C, δ18O) as well as trace elemental compositions have been determined and the comparison of data obtained from these different carbonate archives sheds light on changes in environmental parameters during RFC or FOFC precipitation. References: Richter, D.K., et al., 2011. Radiaxial-fibrous calcites: A new look at an old problem. Sedimentary Geology, 239, 26-36 Richter, D.K., et al., 2015. Radiaxial-fibrous and fascicular-optic Mg-calcitic cave

Origin of dolomites in a downslope biostrome, Jefferson Formation (Frasnian), central Idaho: evidence from REE patterns, stable isotopes, and petrography

Energy Technology Data Exchange (ETDEWEB)

Dorobek, S.L.

1987-08-01

A completely dolomitized coral-stromatoporoid biostrome occurs at the top of the Dark Dolomite member of the Jefferson Formation (Frasnian) at Grandview Canyon, Lost River Range, central Idaho. The biostrome overlies a thick sequence of dolostones that were deposited in slope to deep ramp settings. The biostrome, therefore, formed in an open marine setting after shallowing of deep water environments. Zoned dolospar cement fills dissolution vugs and tectonic fractures. Stable isotopes for zoned dolospar are -13.1 to -6.5 per thousand delta/sup 18/O (average - 11.5) and -1.5 to -0.1 per thousand delta/sup 13/C (average -0.4). REE patterns for zoned dolospar have positive Ce anomalies, but total REE abundance is similar to REE abundance for replacive dolomites. Stratigraphic occurrence in an open marine setting, stable isotopes, and REE patterns suggest replacive dolomite phases formed during shallow burial diagenesis with significant involvement of nonevaporated sea water. More negative Ce anomalies near the top of the biostrome suggest a diagenetic overprint by oxidizing meteoric waters. Zoned dolospar probably formed from warmer, reducing burial fluids. Carbon for zoned dolospar probably was recycled from preexisting dolomite. These data may be useful for interpreting the origin of other anomalous platform dolostones.

The effects of dolomitization on petrophysical properties and fracture distribution within rift-related carbonates (Hammam Faraun Fault Block, Suez Rift, Egypt)

Science.gov (United States)

Korneva, I.; Bastesen, E.; Corlett, H.; Eker, A.; Hirani, J.; Hollis, C.; Gawthorpe, R. L.; Rotevatn, A.; Taylor, R.

2018-03-01

Petrographic and petrophysical data from different limestone lithofacies (skeletal packstones, matrix-supported conglomerates and foraminiferal grainstones) and their dolomitized equivalents within a slope carbonate succession (Eocene Thebes Formation) of Hammam Faraun Fault Block (Suez Rift, Egypt) have been analyzed in order to link fracture distribution with mechanical and textural properties of these rocks. Two phases of dolomitization resulted in facies-selective stratabound dolostones extending up to two and a half kilometers from the Hammam Faraun Fault, and massive dolostones in the vicinity of the fault (100 metres). Stratabound dolostones are characterized by up to 8 times lower porosity and 6 times higher frequency of fractures compared to the host limestones. Precursor lithofacies type has no significant effect on fracture frequency in the stratabound dolostones. At a distance of 100 metres from the fault, massive dolostones are present which have 0.5 times porosity of precursor limestones, and lithofacies type exerts a stronger control on fracture frequency than the presence of dolomitization (undolomitized vs. dolomitized). Massive dolomitization corresponds to increased fracture intensity in conglomerates and grainstones but decreased fracture intensity in packstones. This corresponds to a decrease of grain/crystal size in conglomerates and grainstones and its increase in packstones after massive dolomitization. Since fractures may contribute significantly to the flow properties of a carbonate rock, the work presented herein has significant applicability to hydrocarbon exploration and production from limestone and dolostone reservoirs, particularly where matrix porosities are low.

Petrographic and isotopic evidence for late-stage processes in sulfuric acid caves of the Guadalupe Mountains, New Mexico, USA

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Palmer Arthur N.

2012-07-01

Full Text Available Caves of the Guadalupe Mountains have experienced many modifications since their final phase of sulfuric acid speleogenesis several million years ago. Petrographic and geochemical data reveal details of the change from H2SO4 to CO2-dominated reactions. The H2SO4 dissolution front acquired a coating of replacement gypsum with local pockets of anhydrite and by-products of altered clay, including Fe-Mn oxides. Alteration of bedrock beneath the gypsum produced a white micritized rind with small negative shifts in δ13C and δ18O. Solution basins contain records of the earliest post-speleogenetic processes: corroded bedrock, residual anhydrite, Fe-Mn oxides from fluctuating pH and Eh, mammillary calcite, and dolomitization. Later meteoric water removed or recrystallized much of the gypsum and early micrite, and replaced some gypsum with calcite. Mammillary crusts demonstrate fluctuating groundwater, with calcite layers interrupted by films of Fe-Mn oxides precipitated during periodic inflow of anoxic water. Condensation moisture (from local evaporation absorbs CO2 from cave air, corroding earlier features and lowering their δ13C and δ18O. Drips of condensation water deposit minerals mainly by evaporation, which increases δ18O in the speleothems while δ13C remains nearly constant. By forcing calcite precipitation, evaporation raises the Mg content of remaining water and subsequent precipitates. Dolomite (both primary and replacive is abundant. In areas of low air circulation, water on and within carbonate speleothems equilibrates with cave-air CO2, causing minerals to recrystallize with glassy textures. Fluorite on young evaporative speleothems suggests a recent release of deep-source HF gas and absorption by droplets of condensation water.

Primary Evaporites for the Messinian Salinity Crisis: the shallow gypsum vs. deep dolomite formation paradox solved

Science.gov (United States)

De Lange, Gert J.; Krijgsman, Wout

2014-05-01

mineralization, thus reducing the deep-water sulphate content. In addition, considerable amounts of dissolved carbonate are formed. This means that low-sulphate conditions as for MSC deepwater, i.e. unfavorable conditions for gypsum formation, always coincide with anoxic, i.e. oxygen-free conditions. Thus one would expect a bath-tub rim of gypsum at all shallow depths, but gypsum appears mainly at silled marginal basins. However, a thick package of heavy gypsum on top of more liquid mud in a marginal/slope setting is highly unstable, thus any physical disturbance such as tectonic activity or sea-level change, would easily lead to downslope transport of such marginal gypsum deposits. The absence of gypsum and the presence of erosional unconformities at the sill-less Mediterranean passive margins concord to such removal mechanism. In addition, large-scale re-sedimentation of gypsum has also been found for deep Messinian settings in the Northern Apennines and Sicily. Only at those marginal settings that were silled, the marginal gypsum deposits have been preserved. Including the dynamic biogeochemical processes in the thusfar static interpretations of evaporite formation mechanisms can thus account for the paradoxal, isochronous formation of shallow gypsum and deep-dolomite during the early MSC (1). (1) De Lange G.J. and Krijgsman W. (2010) Mar. Geol. 275, 273-277.

Paleohydrogeological implications from fracture calcites in fissures of low transmissivity. A report of investigations in 2011

International Nuclear Information System (INIS)

Sahlstedt, E.; Karhu, J.

2014-07-01

Samples of fracture fillings were collected from 26 bedrock fractures at Olkiluoto. Special attention was paid to fractures having low transmissivities of <1E-8 m 2 /s. The chemical composition and the C and O isotopic composition of the fracture filling calcite were analysed. In addition, fluid inclusions were studied and microthermometric measurements conducted on fracture filling calcite. The most common minor element in calcite fillings was Mn, having concentrations up to 3.4 wt-%. The δ13C values had a wide range, from -13.0 to 14.5 per mille, and the δ18O values a narrower range, from -13.4 to -7.3 per mille. The δ18O values of late-stage calcite appear to be independent of the transmissivity of the fractures, ranging from -11.2 to -7.3 per mille over a T range from 3E -6 to 1.6E -1 1 m 2 /s. The δ13C values of late-stage calcite appear to have more variation at high transmissivities of >1E-8 m 2 /s. Unusually low and high δ13C values in late-stage calcite fillings occur in the upper ∼ 400 m of the bedrock and are probably related to microbial reduction processes, at near surface (<60 m) conditions to oxidation of organic matter resulting in low δ13C values and at ∼ 55-400 m to methanogenesis, causing high δ 13C values. A relatively low spread in the δ 13C values of late-stage calcite precipitates in low transmissivity (<1E-8 m 2 /s) fractures is most likely caused by stable conditions in the areas of low conductivity in the bedrock, reflecting slow dissolution/reprecipitation of older carbonate fillings. Fluid inclusion data indicate variation in fracture water types from high temperature, ∼ 200 deg C, low salinity fluid with < 4 wt-% of NaCl eq to low temperature, <100 deg C, high salinity fluid with 17-29 wt-% of NaCl eq . The high temperature fluid is associated with Group 5 calcite fillings and the low temperature fluid with Group 3 calcite. The composition of fluids related to Group 4 calcite falls roughly between the compositions

Speleothems from Mawsmai and Krem Phyllut caves, Meghalaya, India: some evidences on biogenic activities

Science.gov (United States)

Baskar, Sushmitha; Baskar, R.; Lee, Natuschka; Theophilus, P. K.

2009-05-01

The Mawsmai cave and Krem Phyllut caves, East Khasi hills, Meghalaya, India has so far not yet attracted the attention of geomicrobiologists. Observations and hypotheses on the possible influence of identified microorganisms for speleothem formations in Meghalaya are reported for the first time. XRD studies identified calcite in speleothems and gypsum in cave wall deposits as the dominant minerals. SEM-EDAX showed interesting microfabric features showing strong resemblance with fossilised bacteria, calcified filaments, needle calcite and numerous nano scale calcite crystals, highly weathered and disintegrated crystals of calcite, that point towards a significant microbial influence in its genesis. Thin section petrography showed laminated stromatolitic features. The microorganisms identified by conventional isolation and further evaluation of isolates by molecular techniques include Bacillus cereus, Bacillus mycoides, Bacillus licheniformis, Micrococcus luteus, and Actinomycetes. Microscopic observations also showed unidentifiable cocci and four unidentifiable strains of CaSO4 (gypsum) precipitating bacteria. Experimental studies confirmed that these bacteria are able to precipitate calcium minerals (calcite, gypsum, minor amounts of dolomite) in the laboratory. These results allow us to postulate that species like these may contribute to active biogenic influence in the cave formations at Meghalaya.

What concentration of actinides can be packed into calcite? Hints from rare earth element (REE) composition

International Nuclear Information System (INIS)

Christiansen, J.; Stipp, S.L.S.; Waight, T.; Baker, J.A.

2005-01-01

Full text of publication follows: For reliable modelling of actinide mobility in the event of spent fuel repository failure, we need data describing the uptake capacity of the minerals likely to find themselves in the transport path. Calcite (CaCO 3 ) is a common secondary mineral in fractures and pore fillings, especially downstream from degrading concrete facilities, so it is a likely candidate for incorporation. Investigations made under ACTAF, a 5. Framework EURATOM integrated project, as well as some other research studies, have shown that actinides are successfully incorporated as substituting ions within the calcite mineral structure. The question remaining, is how much can calcite take up. Geologists routinely use relative concentrations of rare Earth elements (REE's), the lanthanides, for interpreting rock genesis and history. One can also adopt them as analogues for the radioactive elements because their f-orbital electron configuration makes them behave very much like actinides. We collected and analysed a suite of 70 calcite samples from a great number of possible formation environments, geological ages and geographical locations, for the purpose of finding the range and maximum of total f-orbital substitution possible in calcite, under natural conditions. We analysed them using Multi-Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP-MS). The maximum concentration found was about 5 x 10 -3 mole/kg total REE in a sample that had a geological history of formation where REE fluids played a role. Over the whole suite, total REE ranged from less than 10 -4 moles/kg for limestone samples formed from biogenic calcite where REE-enriched fluids would have played a negligible role. Thus, in natural calcite, REE's are present and all evidence points to a structural incorporation within the mineral rather than as a separate REE-rich phase. These data compare favourably with mole fractions from calcite grown synthetically, where as much as 6 x 10 -3

Characterization of marble waste for manufacture of artificial stone; Caracterizacao de residuo de marmore para fabricacao de rocha artificial

Energy Technology Data Exchange (ETDEWEB)

Aguiar, M.C.; Silva, A.G.P., E-mail: maricostalonga2@gmail.com [Universidade Estadual do Norte Fluminense (UENF/LAMAV), Campos dos Goytacazes, RJ (Brazil). Laboratorio de Materiais Avancados; Gadioli, M.C.B. [Centro de Tecnologia Mineral (CETEM/NR-ES), Cachoeiro de Itapemirim, ES (Brazil)

2016-07-01

This work aims to study the characterization of marble waste for the manufacture of artificial stone. The characterization of the waste was performed through X-ray fluorescence, X-ray diffraction, particle size distribution, scanning electron microscopy and confocal microscopy. The results indicated that the marble waste presents typical composition of a dolomite, calcite marble, and their minerals are: Calcite (CaCO{sub 3}) and dolomite (MgCa (CO{sub 3}){sub 2}. The waste presented predominance of particles below 200 mesh screen. This may be interesting for the production of artificial stone better visual appearance, such as marmoglass, for example. The results indicate that the use of marble waste for production of artificial stone is feasible and environmentally friendly alternative to give a destination for this waste generated in the order of millions of tons representing serious environmental problem. (author)

Characterization of marble waste for manufacture of artificial stone

International Nuclear Information System (INIS)

Aguiar, M.C.; Silva, A.G.P.

2016-01-01

This work aims to study the characterization of marble waste for the manufacture of artificial stone. The characterization of the waste was performed through X-ray fluorescence, X-ray diffraction, particle size distribution, scanning electron microscopy and confocal microscopy. The results indicated that the marble waste presents typical composition of a dolomite, calcite marble, and their minerals are: Calcite (CaCO_3) and dolomite (MgCa (CO_3)_2. The waste presented predominance of particles below 200 mesh screen. This may be interesting for the production of artificial stone better visual appearance, such as marmoglass, for example. The results indicate that the use of marble waste for production of artificial stone is feasible and environmentally friendly alternative to give a destination for this waste generated in the order of millions of tons representing serious environmental problem. (author)

Rearrangement of porous CaO aggregates during calcite decomposition in vacuum

International Nuclear Information System (INIS)

Beruto, D.; Barco, L.; Searcy, A.W.

1983-01-01

High-resolution SEM photographs, N 2 adsorption isotherms, Hg porosimetry, and micrometer measurements were used to characterize CaO particle shapes and pore-size distributions that result when calcite crystals are decomposed in vacuum at 686 0 C. The surface area of the CaO produced from large calcite crystals is constant at 116 + or - 4 m 2 /g independent of the extent of reaction. The volume occupied by a CaO aggregate is approx. = 98 + or - 2% that of the original calcite crystal. The approx. = 54% total porosity is comprised of 42% pores of approx. = 5 nm cross section and 12% pores of approx. = 10 μm cross section. The duplex pore structure is formed by a diffusionless repacking of CaO particles that initially form with a more uniform distribution of particles and pores

Removal of Phosphate from Synthetic Aqueous Solution by Adsorption with Dolomite from Padalarang

Directory of Open Access Journals (Sweden)

Fadjari Lucia Nugroho

2014-12-01

Full Text Available The presence of phosphate in wastewaters can cause eutrophication of surface water bodies leading to algal-blooming in the aquatic environment and degradation of water quality. Phosphate removal from wastewaters by conventional biological treatment removes only 10-30% of the phosphate, whilst chemical treatment using precipitants such as calcium or iron salts, although effective, is expensive and produces water-rich sludge which must be further treated. Hence, phosphate removal by adsorption in the form of Ca -phosphate has been proposed as an alternative to the more traditional methods. This study investigated the feasibility of using dolomite–a common sedimentary rock–from Padalarang, West Java, Indonesia as the adsorbent for the removal of phosphate from synthetic aqueous solution. Chemical analysis revealed that the Padalarang dolomite contains 33.6-36.2% CaO. Batch experiments at room temperature indicated that optimum removal of phosphate was achieved at pH 9. At 25°C , where increasing concentrations of phosphate (10–100 mg/L increased phosphate adsorption (2.15-31.3 mg/g by the dolomite. The adsorption of phosphate could be described by the Langmuir isotherm model, with constants Qm= 476.19 mg/g, K L= 0,00106 L/mg and equilibrium parameter (R L: 0.904 – 0.989. Phosphate adsorption by dolomite not only permits its removal but also its potential recovery for reuse.

A time-resolved laser fluorescence spectroscopy (TRLFS) study of the interaction of trivalent actinides (curium(III)) with calcite

International Nuclear Information System (INIS)

Stumpf, Th.; Fanghaenel, Th.

2002-01-01

Cm(III) interaction with calcite was investigated in the trace concentration range. Two different Cm(III)/calcite sorption species were found. The first Cm(III) sorption species consists of a curium ion that is bonded onto the calcite surface. The second Cm(III) sorption species has lost its complete hydration sphere and is incorporated into the calcite bulk structure /1/. (orig.)

Depositional environments and porosity distribution in regressive limestone reservoirs of the Mishrif Formation, Southern Iraq

International Nuclear Information System (INIS)

AlDabbas, Moutaz; AlJassim Jassim; AlJumaily Saad

2010-01-01

Eight subsurface sections and a large number of thin sections of the Mishrif Limestone were studied to unravel the depositional facies and environments. The allochems in the Mishrif Formation are dominated by bioclasts, whereas peloids, ooids, and intraclasts are less abundant. The sedimentary microfacies of the Mishrif Formation includes mudstone, wackestone, packstone, grainstone, floatstone, and rudstone, which have been deposited in basinal, outer shelf, slop followed by shoal reef and lagoonal environments. The formation displays various extents of dolomitization and is cemented by calcite and dolomite. The formation has gradational contact with the underlying Rumaila Formation but is unconformably overlain by the Khasib Formation. The unconformity is recognized because the skeletal grains are dominated by Chaophyta (algae), which denotes the change of environment from fully marine to lacustrine environment. Thus, the vertical bioclast analysis indicates that the Mishrif Formation is characterized by two regressive cycles, which control the distribution of reservoir quality as well as the patterns of calcite and dolomite cement distribution. Mishrif Formation gradationally overlies Rumaila Formation. This was indicated by the presence of the green parts of Chaophyta (algae) as main skeletal grains at the uppermost part of well Zb-47, which refer to lacustrine or fresh water environment. Petrographical study shows that the fossils, peloids, oolitis, and intraclasts represent the main allochem. Calcite and dolomite (as diagenetic products) are the predominant mineral components of Mishrif Formation. Fossils were studied as an environmental age and facial boundaries indicators, which are located in a chart using personal computer programs depending on their distributions on the first appearance of species. Fifteen principal sedimentary microfacies have been identified in the Mishrif Formation, which includes lime mudstone, mudstone-wackestone, wackestone

CaCO3-III and CaCO3-VI, high-pressure polymorphs of calcite: Possible host structures for carbon in the Earth's mantle

Science.gov (United States)

Merlini, M.; Hanfland, M.; Crichton, W. A.

2012-06-01

time, Mg and Fe solubility in aragonite is hindered energetically in the 9-fold coordination site. Above 15 GPa, and up to the maximum pressure investigated (40 GPa), we observe the high-pressure polymorph CaCO3-VI, triclinic [a=3.3187(12) Å, b=4.8828(14) Å, c=5.5904(14) Å, α=103.30(2)°, β=94.73(2)°, γ=89.21(2)°, V=87.86(20) Å3 at 30.4 GPa] with 10 atoms in the unit cell. It is characterised by coplanar CO3 groups but the structure is no longer layered, as in the lower pressure polymorphs. The density of the CaCO3-VI structure (3.78 g/cm3 at 30.4 GPa) is higher than aragonite. For this reason it could be supposed that a region may exist where this polymorph replaces aragonite in the Earth's intermediate mantle. The lower coordination number for the Ca site [7+2] instead of [9] in aragonite suggests that this structure could be easily adopted by an extended solid-solution range from calcite towards the dolomite [CaMg(CO3)2]-ankerite [CaFe(CO3)2] compositional join. The transitions from calcite to CaCO3-III, CaCO3-IIIb and CaCO3-VI are perfectly reversible and after pressure release we always observe the calcite structure, with the sample recovered as a single-crystal. Indeed, it is highly unlikely that these structures can be observed in samples recovered from high-pressure environments.

Thermal and catalytic cracking of ethylene in presence of CaO, MgO, zeolite and calcined dolomite

Energy Technology Data Exchange (ETDEWEB)

Taralas, G; Sjoestroem, K; Jaeraas, S; Bjoernbom, E [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Chemical Technology

1994-12-31

The subject of the present work is to study the effect of catalysts such as calcined dolomite (CaO.MgO), CaO (quicklime), MgO and Zeolite (EKZ-4) on the cracking of ethylene in the presence and absence of steam. N-heptane, toluene, naphthalene, thiophene have been some suitable model compounds for studies of the thermal and catalytic decomposition of tar. Previous results showed that the reaction scheme of the thermal decomposition of n-heptane was consistent with the high yield of ethylene observed in thermal decomposition of n-heptane. The effect of the reactor wall and the ferric impurities in the dolomite are also subjects of the research in this study. The results may also throw some additional light on the nature of the gas-phase thermal and catalytic reactions occurring in the use of dolomite as tar cracking catalysts. 28 refs

Geochemical evolution of groundwater in carbonate aquifers of southern Latium region, central Italy

Directory of Open Access Journals (Sweden)

Giuseppe Sappa

2013-03-01

Full Text Available Spring and well water samples, from carbonate aquifers of Latium region, have been characterized to determine the hydrochemical processes governing the evolution of the groundwater. Most of the spring samples, issuing from Lepini, Ausoni and Aurunci Mts., are characterized as alkaline earth HCO3 waters, however, some samples show a composition of Cl--SO4 -- alkaline earth waters. Groundwater samples from Pontina Plain shows three different hydrochemical facies: alkaline earth HCO3 type, Cl-- SO4 -- alkaline earth type and Cl--SO4 -- alkaline type waters. Geochemical modeling and saturation index computation of the sampled waters show an interaction with calcareous and calcareous-dolomitic lithologies. Most of the springs and wells was kinetically saturated with respect to calcite and dolomite, and all the samples were below the equilibrium state with gypsum. This indicates that the groundwater has capacity to dissolve the gypsum along the flow paths. The electrical conductivity and Cl- concentrations of the sampled waters show a positive trend with the decrease in the distance from the coast, highlighting seawater intrusion in the coastal area. According to hydrochemistry results and geochemical modeling, the dominant factors in controlling the hydrochemical characteristics of groundwater are: (i water rock interaction with calcareous and calcareous-dolomitic lithologies; (ii seawater intrusion in the coastal area; (iii dissolution and/or precipitation of carbonate and (i.e. dolomite and calcite evaporate minerals (gypsum determined by saturation indexes; (iv mineral weathering process; (the high Mg/Ca ratio due to the weathering of Mg-rich dolomite.

Ferroan dolomite cement in Cambrian sandstones: burial history and hydrocarbon generation of the Baltic sedimentary basin

DEFF Research Database (Denmark)

Sliaupa, S.; Cyziene, J.; Molenaar, Nicolaas

2008-01-01

The conditions and timing of carbonate cementation in Cambrian sandstones of the Baltic sedimentary basin were determined by oxygen and carbon stable isotope and chemical data in combination with optical and cathodoluminescence petrographic studies. Studied samples represent a range in present...... burial depth from 340 to 2150 m. The carbonate cement is dominantly ferroan dolomite that occurs as dispersed patches of poikilotopic crystals. Temperatures of dolomite precipitation, based on delta O-18 values, range from 27 degrees C in the shallow buried to 95 degrees C in the deep buried sandstones...

Investigation of the interaction of Greek dolomitic marble with metal aqueous solutions using Rutherford backscattering and X-ray photoelectron spectroscopy

International Nuclear Information System (INIS)

Godelitsas, A.; Kokkoris, M.; Misaelides, P.

2005-01-01

The interaction of dolomitic marble from Thassos Island (northern Aegean sea, Greece) with Co 2+ -, Cd 2+ -, Pb 2+ - and Cr 3+ - aqueous solutions (metal concentration: 1000 mgL -1 ) was investigated using Rutherford backscattering (RBS) and X-ray photoelectron spectroscopy (XPS). The initial material as well as the interaction products were also characterized by scanning electron microscopy (SEM/EDS), radioisotope induced X-ray fluorescence analysis (RI-XRFA), powder X-ray diffraction (Powder-XRD) and Fourier transform infra-red spectroscopy (FT-IR). The contact time of the samples with the aqueous solutions was one week and took place under ambient temperature. To our knowledge, the sorption of the above mentioned metals with dolomite (CaMg(CO 3 ) 2 ) has not yet been presented in the literature and the only data available concern the adsorption of Ca, Mg and Nd from NaCl solutions. The Thassos island dolomitic marble is a snow-white homogeneous carbonate metamorphic rock, with fine physicochemical and mechanical properties, currently used as natural building stone in many parts of the world (see http://www.thassosmarble.com), This dolomite-bearing material was also extensively used in the past as construction material of many .classical Greek and Roman sculptures and architectural elements; in 301 AD the Roman emperor Diocletian included 'Thassian marble' in the list of the 19 most expensive and important 'marbles' produced in the imperial quarries. Previous literature presented the isotopic analysis(δ 13 C, δ 18 O) and EPR studies (Mn 2+ and Fe 3+ ) of this stone. The obtained results indicated a limited Cd 2+ - and Co 2+ -sorption on the dissolved surface of the carbonate substrate, whereas, under the same experimental conditions, the Pb 2+ - and Cr 3+ -interaction is more intense leading to extended overgrowth of crystalline Pb-carbonates and surface precipitation of amorphous Cr-hydroxides/oxyhydroxides.

Cyclic Cratonic Carbonates and Phanerozoic Calcite Seas.

Science.gov (United States)

Wilkinson, Bruce H.

1982-01-01

Discusses causes of cyclicity in cratonic carbonate sequences and evidence for and potential significance of postulated primary calcite sediment components in past Paleozoic seas, outlining problems, focusing on models explaining existing data, and identifying background. Future sedimentary geologists will need to address these and related areas…

Diagenesis and reservoir quality evolution of palaeocene deep-water, marine sandstones, the Shetland-Faroes Basin, British continental shelf

Energy Technology Data Exchange (ETDEWEB)

Mansurbeg, H. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Morad, S. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Department of Petroleum Geosciences, The Petroleum Institute, P.O. Box 2533, Abu Dhabi (United Arab Emirates); Salem, A. [Faculty of Education at Kafr El-Sheikh, Tanta University, Kafr El-Sheikh (Egypt); Marfil, R.; Caja, M.A. [Departmento Petrologia y Geoquimica, Facultad de Geologia, UCM, 28040 Madrid (Spain); El-ghali, M.A.K. (Geology Department, Al-Fateh University, P.O. Box 13696, Libya); Nystuen, J.P. [Department of Geosciences, University of Oslo, P.O. Box 1047 Blindern, NO-0316 Oslo (Norway); Amorosi, A. [Department of Earth Sciences, University of Bologna, Via Zamboni 67, 40127 Bologna (Italy); Garcia, D. [Centre SPIN, Department GENERIC, Ecole Nationale Superieure des Mines de Saint Etienne 158, Cours Fauriel 42023, Saint-Etienne (France); La Iglesia, A. [Instituto de Geologia Economica (CSIC-UCM), Facultad de Geologia, UCM, 28040 Madrid (Spain)

2008-06-15

The Palaeocene, deep-water marine sandstones recovered from six wells in the Shetland-Faroes Basin represent lowstand, transgressive and highstand systems tract turbiditic sediments. Mineralogic, petrographic, and geochemical analyses of these siliciclastics are used to decipher and discuss the diagenetic alterations and subsequent reservoir quality evolution. The Middle-Upper Palaeocene sandstones (subarkoses to arkoses) from the Shetland-Faroes Basin, British continental shelf are submarine turbiditic deposits that are cemented predominantly by carbonates, quartz and clay minerals. Carbonate cements (intergranular and grain replacive calcite, siderite, ferroan dolomite and ankerite) are of eogenetic and mesogenetic origins. The eogenetic alterations have been mediated by marine, meteoric and mixed marine/meteoric porewaters and resulted mainly in the precipitation of calcite ({delta}{sup 18}O{sub V-PDB}=-10.9 permille and -3.8 permille), trace amounts of non-ferroan dolomite, siderite ({delta}{sup 18}O{sub V-PDB}=-14.4 permille to -0.6 permille), as well as smectite and kaolinite in the lowstand systems tract (LST) and highstand systems tract (HST) turbiditic sandstone below the sequence boundary. Minor eogenetic siderite has precipitated between expanded and kaolinitized micas, primarily biotite. The mesogenetic alterations are interpreted to have been mediated by evolved marine porewaters and resulted in the precipitation of calcite ({delta}{sup 18}O{sub V-PDB}=-12.9 permille to -7.8 permille) and Fe-dolomite/ankerite ({delta}{sup 18}O{sub V-PDB}=-12.1 permille to -6.3 permille) at temperatures of 50-140 and 60-140 C, respectively. Quartz overgrowths and outgrowth, which post- and pre-date the mesogenetic carbonate cements is more common in the LST and TST of distal turbiditic sandstone. Discrete quartz cement, which is closely associated with illite and chlorite, is the final diagenetic phase. The clay minerals include intergranular and grain replacive

Relative Abundances of Calcite and Silica in Fracture Coatings as a Possible Indicator of Evaporation in a Thick Unsaturated Zone, Yucca Mountain, Nevada

Science.gov (United States)

Marshall, B. D.; Moscati, R. J.

2005-12-01

Yucca Mountain, a ridge of shallowly dipping, Miocene-age volcanic rocks in southwest Nevada, is the proposed site for a nuclear waste repository to be constructed in the 500- to 700-m-thick unsaturated zone (UZ). At the proposed repository, the 300-m-thick Topopah Spring Tuff welded unit (TSw) is overlain by approximately 30 m of nonwelded tuffs (PTn); the Tiva Canyon Tuff welded unit (TCw) overlies the PTn with a range in thickness from 0 to approximately 130 m at the site. The amount of water percolation through the UZ is low and difficult to measure directly, but local seepage into mined tunnels has been observed in the TCw. Past water seepage in the welded tuffs is recorded by widespread, thin (0.3 cm) coatings of calcite and silica on fracture surfaces and within cavities. Abundances of calcite and silica in the coatings were determined by X-ray microfluorescence mapping and subsequent multispectral image analysis of over 200 samples. The images were classified into constituent phases including opal-chalcedony-quartz (secondary silica) and calcite. In the TCw samples, the median calcite/silica ratio is 8; in the TSw samples within 35 m below the PTn, median calcite/silica falls to 2, perhaps reflecting an increase in soluble silica from the presence of glass in the nonwelded tuffs. In the deeper parts of the TSw, median calcite/silica reaches 100 and many samples contain no detectable secondary silica phase. Evaporation and changing pCO2 control precipitation of calcite from water percolating downward in the UZ, but precipitation of opal requires only evaporation. Calcite/silica ratios, therefore, can constrain the relative importance of evaporation in the UZ. Although calcite/silica values scatter widely within the TSw, reflecting the spatial variability of gas and water flow, average calcite/silica ratios increase with stratigraphic depth, indicating less evaporation at the deeper levels of the UZ. Coupled with the much smaller calcite/silica ratios

Establishing the Relationship between Fracture-Related Dolomite and Primary Rock Fabric on the Distribution of Reservoirs in the Michigan Basin

Energy Technology Data Exchange (ETDEWEB)

G. Michael Grammer

2006-09-30

This topical report covers the year 2 of the subject 3-year grant, evaluating the relationship between fracture-related dolomite and dolomite constrained by primary rock fabric in the 3 most prolific reservoir intervals in the Michigan Basin (Ordovician Trenton-Black River Formations; Silurian Niagara Group; and the Devonian Dundee Formation). The characterization of select dolomite reservoirs has been the major focus of our efforts in Phase II/Year 2. Fields have been prioritized based upon the availability of rock data for interpretation of depositional environments, fracture density and distribution as well as thin section, geochemical, and petrophysical analyses. Structural mapping and log analysis in the Dundee (Devonian) and Trenton/Black River (Ordovician) suggest a close spatial relationship among gross dolomite distribution and regional-scale, wrench fault related NW-SE and NE-SW structural trends. A high temperature origin for much of the dolomite in the 3 studied intervals (based upon initial fluid inclusion homogenization temperatures and stable isotopic analyses,) coupled with persistent association of this dolomite in reservoirs coincident with wrench fault-related features, is strong evidence for these reservoirs being influenced by hydrothermal dolomitization. For the Niagaran (Silurian), a comprehensive high resolution sequence stratigraphic framework has been developed for a pinnacle reef in the northern reef trend where we had 100% core coverage throughout the reef section. Major findings to date are that facies types, when analyzed at a detailed level, have direct links to reservoir porosity and permeability in these dolomites. This pattern is consistent with our original hypothesis of primary facies control on dolomitization and resulting reservoir quality at some level. The identification of distinct and predictable vertical stacking patterns within a hierarchical sequence and cycle framework provides a high degree of confidence at this point

Selection strategy for the most Suitable CEC method for clay barrier characterisation

International Nuclear Information System (INIS)

Dohrmann, R.; Kaufhold, S.

2010-01-01

competition to barium ions in smectite interlayers. The present study aims at proposing a selection strategy for CEC methods including exchangeable cation determination of different clay materials typically used in radioactive waste disposal studies. 1) If the clay/bentonite contains calcium carbonates but no gypsum several methods are available, all of them are based on a saturation of the exchange solution with calcite before the exchange experiment starts: AgTU-calcite, CoHex-calcite, and Cu-trien5xcalcite. If dolomite is present the initial calcite saturation minimizes dolomite dissolution as well (proved for AgTU-calcite). 2) If a bentonite contains carbonates and gypsum the only known successful method for determination of all exchangeable cations (including calcium) and the CEC is a combination of two separate results: i) calcite saturation of exchange solution (e.g. Cu-trien5xcalcite) and ii) quantification of gypsum with suitable mineralogical methods. Result i) is free of error caused by calcite dissolution; however it is still wrong because it contains significant amounts of Ca 2+ from gypsum dissolution. After proving that gypsum was completely dissolved during the exchange experiment result ii) was used to subtract the theoretical Ca 2+ portion of gypsum from result i). Gypsum saturation of exchange solutions was tested as not suitable owing to the high solubility of gypsum which results in high initial Ca 2+ concentrations. 3) If no such soluble minerals are present and if the pore water contains no excess electrolyte then usually any accepted CEC method can be used, however, the results should always be checked for plausibility (e.g. using mineralogical composition of the sample). Any accepted method means that methods with known systematic errors (hydrophobic interaction, dependency on layer charge density) are excluded. (authors)

Experimental diagenesis: insights into aragonite to calcite transformation of Arctica islandica shells by hydrothermal treatment

Science.gov (United States)

Casella, Laura A.; Griesshaber, Erika; Yin, Xiaofei; Ziegler, Andreas; Mavromatis, Vasileios; Müller, Dirk; Ritter, Ann-Christine; Hippler, Dorothee; Harper, Elizabeth M.; Dietzel, Martin; Immenhauser, Adrian; Schöne, Bernd R.; Angiolini, Lucia; Schmahl, Wolfgang W.

2017-03-01

Biomineralised hard parts form the most important physical fossil record of past environmental conditions. However, living organisms are not in thermodynamic equilibrium with their environment and create local chemical compartments within their bodies where physiologic processes such as biomineralisation take place. In generating their mineralised hard parts, most marine invertebrates produce metastable aragonite rather than the stable polymorph of CaCO3, calcite. After death of the organism the physiological conditions, which were present during biomineralisation, are not sustained any further and the system moves toward inorganic equilibrium with the surrounding inorganic geological system. Thus, during diagenesis the original biogenic structure of aragonitic tissue disappears and is replaced by inorganic structural features. In order to understand the diagenetic replacement of biogenic aragonite to non-biogenic calcite, we subjected Arctica islandica mollusc shells to hydrothermal alteration experiments. Experimental conditions were between 100 and 175 °C, with the main focus on 100 and 175 °C, reaction durations between 1 and 84 days, and alteration fluids simulating meteoric and burial waters, respectively. Detailed microstructural and geochemical data were collected for samples altered at 100 °C (and at 0.1 MPa pressure) for 28 days and for samples altered at 175 °C (and at 0.9 MPa pressure) for 7 and 84 days. During hydrothermal alteration at 100 °C for 28 days most but not the entire biopolymer matrix was destroyed, while shell aragonite and its characteristic microstructure was largely preserved. In all experiments up to 174 °C, there are no signs of a replacement reaction of shell aragonite to calcite in X-ray diffraction bulk analysis. At 175 °C the replacement reaction started after a dormant time of 4 days, and the original shell microstructure was almost completely overprinted by the aragonite to calcite replacement reaction after 10 days

Nucleation, growth and evolution of calcium phosphate films on calcite.

Science.gov (United States)

Naidu, Sonia; Scherer, George W

2014-12-01

Marble, a stone composed of the mineral calcite, is subject to chemically induced weathering in nature due to its relatively high dissolution rate in acid rain. To protect monuments and sculpture from corrosion, we are investigating the application of thin layers of hydroxyapatite (HAP) onto marble. The motivation for using HAP is its low dissolution rate and crystal and lattice compatibility with calcite. A mild, wet chemical synthesis route, in which diammonium hydrogen phosphate salt was reacted with marble, alone and with cationic and anionic precursors under different reaction conditions, was used to produce inorganic HAP layers on marble. Nucleation and growth on the calcite substrate was studied, as well as metastable phase evolution, using scanning electron microscopy, grazing incidence X-ray diffraction, and atomic force microscopy. Film nucleation was enhanced by surface roughness. The rate of nucleation and the growth rate of the film increased with cationic (calcium) and anionic (carbonate) precursor additions. Calcium additions also influenced phase formation, introducing a metastable phase (octacalcium phosphate) and a different phase evolution sequence. Copyright © 2014 Elsevier Inc. All rights reserved.

A thermoluminescence study of vempalle dolomites and its depositional environments

International Nuclear Information System (INIS)

Bhattacharya, A.K.; Rao, C.N.; Kaul, I.K.

1976-01-01

An attempt has been made to interpret the depositional environment of Vempalle dolomites (India) by thermoluminescence method. It has been demonstrated that glow curve patterns reflect the environmental condition of deposition for carbonate sediments. The glow curves were obtained for natural samples as well as samples irradiated by Co 60 and compared. A majority of the samples were concluded to be diagenetic. (A.K.)

Sealing of rock joints by induced calcite precipitation. A case study from Bergeforsen hydro power plant

International Nuclear Information System (INIS)

Hakami, E.; Qvarfort, U.; Ekstav, A.

1991-01-01

The possibilities of sealing rock fractures by injecting water saturated with calcite solution, and hereby inducing a calcite precipitation inside the fracture, is investigated. The way of reaction and the amount of calcite precipitation will depend on the saturation of calcium carbonate in the water, the temperature, the pH and the CO 2 -pressure. There is experience of lime-saturated water injection in the rock foundation below the dam at Bergeforsens power plant (1955-1968). It was observed that the consumption of injected lime water decreased with time. A possible reason to the decrease in lime water consumption is that calcite has precipitated such that the permeability of the rock in general is lowered. Another explanation to this could be that calcite precipitation is concentrated to the fractures surrounding the injection holes, thus preventing the lime water from penetrating further into the rock. It is recommended that further studies of the fracture fillings in drill cores from Bergeforsen is performed. The aim of such study should be to determine the extent of induced calcite precipitation and to investigate its chemical and physical properties. (authors)

Characterization of the main types of marble extracted in the area of Macael (Almeria, southeastern Spain) and its historical importance

International Nuclear Information System (INIS)

Navarro, R.; Cruz, A.S.; Arriaga, L.; Baltuille, J.M.

2017-01-01

The marble from Macael is one of the most important ornamental stones found in Spain. It has been used not only as a building material but also as a decorative element, especially the type nown as “White Macael “. There is evidence of its use dating back over 4000 years. One of the most prominent examples is the Courtyard of the Lions in the Alhambra (Granada), but it is also possible to see some eleme Its in the Roman amphitheatre of Mérida (Badajoz), in Italica (Sevilla), in the palace of Medina Azahara (Córdoba) and in the Royal Palace of Madrid, amongst dozens of palaces and churches throughout the country. In this study we describe the use that this material has had throughout history and the main features and properties of the different varieties of “White Macael”, “Grey Macael”, “Anasol” (calcite marbles) and “Yellow Macael” (dolomitic marbles). They all have mineralogical, physical and mechanical features that make them suitable for almost all uses. Calcite marbles have porosity, absorption and density values lower than dolomite marbles, whilst the latter have more resistance to compression, similar flexural strength under concentrated load, and lower resistance to breaking load at dowel hole than the calcitic marbles. The values of abrasion resistance are also better in the dolomite marbles, whilst the slip resistance is similar in all cases. As far as decay is concerned, the dolomitic marbles, with the exception of the variety Amarillo Triana, suffer more in the frost resistance test but less by the action of salts, with the exception of the White Macael Rio (calcitic) which is the variety that has less alteration. Regarding the status of the stone sector in the region, it is noteworthy that, despite a 60% drop in sales in the domestic market, exports in 2012 increased by 49 % compared to the previous year. The data we present provides increased knowledge of one of the most common building materials in our country with the aim of

Rare Earth element (REE) incorporation in natural calcite. Upper limits for actinide uptake in a secondary phase

International Nuclear Information System (INIS)

Stipp, S.L.S.; Christensen, J.T.; Waight, T.E.; Lakshtanov, L.Z.; Baker, J.A.

2006-01-01

Secondary minerals have the potential to sequester escaped actinides in the event of a radioactive waste repository failure, but currently, data to define their maximum uptake capacity are generally lacking. To estimate a maximum limit for solid solution in calcite, we took advantage of the behavioural similarities of the 4f-orbital lanthanides with some of the 5f-orbital actinides and used rare Earth element (REE) concentration as an analogue. A suite of 65 calcite samples, mostly pure single crystals, was assembled from a range of geological settings, ages and locations and analysed by isotope dilution MC-ICP-MS (multiple-collector inductively-coupled plasma mass spectroscopy). All samples were shown to contain significant lanthanide concentrations. The highest were in calcite formed from hydrothermal solutions and from carbonatite magma. Maximum total mole fraction of REE was 4.72 x 10 -4 , which represents one substituted atom for about 2000 Ca sites. In comparison, synthetic calcite, precipitated at growth rates slow enough to insure solid solution formation, incorporated 7.5 x 10 -4 mole fraction Eu(III). For performance assessment, we propose that 7.5 mmole substitution/kg calcite should be considered the upper limit for actinide incorporation in secondary calcite. The largest source of uncertainty in this estimate results from extrapolating lanthanide data to actinides. However, the data offer confidence that for waters in the hydrothermal temperature range, such as in the near-field, or at groundwater temperatures, such as in the far-field, if calcite formation is favoured and actinides are present, those with behaviour like the trivalent lanthanides, especially Am 3+ and Cm 3+ , will be incorporated. REE are abundant and widely distributed, and they have remained in calcite for millions of years. Thus, one can be certain that incorporated actinides will also remain immobilised in calcite formed in fractures and pore spaces, as long as solution conditions

The Elemental content of Niue Island soils as an indicator of their origin

International Nuclear Information System (INIS)

Whitehead, N.E.

1993-01-01

The major and trace element contents of 241 Niue Island lateritic soils were determined, mainly by X-ray fluorescence, to deduce soil origins. The analyses showed very low SiO 2 content, and a high content of Mg, P, V, Cr, Sr, Y, Hg, and α-counts, compared with other laterites worldwide. The distribution patterns are consistent with derivation by weathering from calcite and dolomite rather then from deposted volcanic ash. Weathering is a particularly novel explanation for the origin of the relatively high content of P in these soils. The soils contain a negative Ce anomly, consistent with an origin from seawater or coral, but not volcanic ash. If recent results showing in situ formation of magnetite in soils are applicable, the soil mineralogy is wholly from calcite is also consistent with the relative lack of volcanic ash on the seabed nearby, and very low deposition of aeolian dust. The radioactivity content is consistent neither with calcite/dolomite wathering, nor volcanic ash orgin, but may have originated, like a few of the stable elements, from rising hydrothermal solutions. (authors). 67 refs.; 8 figs.; 6 tabs

Attrition of Dolomitic Lime in a Fluidized-Bed at High Temperature

Czech Academy of Sciences Publication Activity Database

Hartman, Miloslav; Svoboda, Karel; Pohořelý, Michael; Šyc, Michal; Jeremiáš, Michal

2013-01-01

Roč. 67, č. 2 (2013), s. 164-172 ISSN 0366-6352 R&D Projects: GA AV ČR IAA400720701; GA MŠk(CZ) 7C11009 Grant - others:RFCS(XE) RFCR-CT-2010-00009 Institutional support: RVO:67985858 Keywords : attrition * catalytic gasification * dolomitic lime Subject RIV: CI - Industrial Chemistry, Chemical Engineering Impact factor: 1.193, year: 2013

Adsorption of pesticides onto quartz, calcite, kaolinite, and α-alumina

DEFF Research Database (Denmark)

Clausen, Liselotte; Fabricius, Ida Lykke; Madsen, L.

2001-01-01

adsorption characteristics of selected pesticides. Investigated mineral phases included quartz, calcite, kaolinite, and alpha -alumina. Selected pesticides comprised atrazine (6-chloro-N-2-ethyl-N-4-isopropyl-1,3,5-triazine-2,4-diamine isoproturon [3-(4-isopropyl-phenyl)-1,1-dimethylurea)], mecoprop [(RS)-2...... due to formation of Ca-pesticide-surface complexes. Adsorption of the uncharged pesticides (atrazine and isoproturon) was detected only on kaolinite. The lack of adsorption on alpha -alumina indicates that the uncharged pesticides have a greater affinity for the silanol surface sites (= SiOH) than...

Precipitation of Calcite during the Deposition of Paleogene Sangkarewang Oil Shale, Ombilin Basin, West Sumatra, Indonesia

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Agus Haris Widayat

2015-09-01

Full Text Available DOI: 10.17014/ijog.2.3.185-197Geochemical and petrographical analyses were carried out to investigate the occurrence of calcite in theformer Ombilin lacustrine lake. The study involves eight samples taken from a 56 m long drill core of Sangkarewangoil shale. Geochemical investigation showed that the samples consist of varied terrigenous input represented by Si, Al, K, and Ti, and autochthonous input represented by S, total organic carbon (TOC, and d13C of bulk organic matter. Along the drill core profile the abundance of autochthonous input decreases upwards, while that of terrigenous input oppositely increases upwards. Petrographical analysis revealed that calcite is a major mineral in the samples. In this study, the abundance of calcite could be represented by the abundance of Ca, as calcite is the only significant Ca containing mineral. Ca is abundant in the samples (8.4% in average and its concentration varies similarly with those of S, TOC, and d13C, suggesting that the element as well as calcite incorporates the autochthonous input. Thevariation of calcite abundance in the drill core profile is considered to be related with primary productivity changes during the development of the former lake. Higher primary productivity represented by more positive of d13C value(-24.8‰ during the deposition of the lower part of the drill core profile promoted the higher amount of deposited organic matter. In such environment, the supersaturation of carbonate ion in lake water was also reached and significant precipitation of authigenic calcite occurred. As the lake developed, the primary productivity decreased as indicated by more negative of d13C value (eventually -26.8‰. This condition led to the decreases of deposited organic matterand calcite in the lake sediments.

Molecular dynamics simulation of the rotational order-disorder phase transition in calcite

International Nuclear Information System (INIS)

Kawano, Jun; Miyake, Akira; Shimobayashi, Norimasa; Kitamura, Masao

2009-01-01

Molecular dynamics (MD) simulation of calcite was carried out with the interatomic potential model based on ab initio calculations to elucidate the phase relations for calcite polymorphs and the mechanism of the rotational order-disorder transition of calcite at high temperature at the atomic scale. From runs of MD calculations with increasing temperature within a pressure range of 1 atm and 2 GPa, the transition of calcite with R3-barc symmetry into a high-temperature phase with R3-barm symmetry was reproduced. In the high-temperature R3-barm phase, CO 3 groups vibrate with large amplitudes either around the original positions in the R3-barc structure or around other positions rotated ± 60 deg., and their positions change continuously with time. Moreover, contrary to the suggestion of previous investigators, the motion of CO 3 groups is not two-dimensional. At 1 atm, the transition between R3-barc and R3-barm is first order in character. Upon increasing temperature at high pressure, however, first a first-order isosymmetric phase transition between the R3-barc phases occurs, which corresponds to the start of ± 120 deg. flipping of CO 3 groups. Then, at higher temperatures, the transition of R3-barc to R3-barm phases happens, which can be considered second order. This set of two types of transitions at elevated pressure can be characterized by the appearance of an 'intermediate' R3-barc phase between the stable region of calcite and the high-temperature R3-barm phase, which may correspond to the CaCO 3 -IV phase.

Competitive adsorption of arsenate and phosphate onto calcite; experimental results and modeling with CCM and CD-MUSIC

DEFF Research Database (Denmark)

Sø, Helle Ugilt; Postma, Dieke; Jakobsen, Rasmus

2012-01-01

The competitive adsorption of arsenate and phosphate onto calcite was studied in batch experiments using calcite-equilibrated solutions. The solutions had circum-neutral pH (7–8.3) and covered a wide span in the activity of Ca2+ and View the MathML source. The results show that the adsorption...... that adsorption of arsenate onto calcite is of minor importance in most groundwater aquifers, as phosphate is often present at concentration levels sufficient to significantly reduce arsenate adsorption. The CD-MUSIC model for calcite was used successfully to model adsorption of arsenate and phosphate separately...

Simulated oxygen isotopes in cave drip water and speleothem calcite in European caves

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A. Wackerbarth

2012-11-01

Full Text Available Interpreting stable oxygen isotope (δ¹⁸O records from stalagmites is still one of the complex tasks in speleothem research. Here, we present a novel model-based approach, where we force a model describing the processes and modifications of δ¹⁸O from rain water to speleothem calcite (Oxygen isotope Drip water and Stalagmite Model – ODSM with the results of a state-of-the-art atmospheric general circulation model enhanced by explicit isotope diagnostics (ECHAM5-wiso. The approach is neither climate nor cave-specific and allows an integrated assessment of the influence of different varying climate variables, e.g. temperature and precipitation amount, on the isotopic composition of drip water and speleothem calcite.

First, we apply and evaluate this new approach under present-day climate conditions using observational data from seven caves from different geographical regions in Europe. Each of these caves provides measured δ¹⁸O values of drip water and speleothem calcite to which we compare our simulated isotope values. For six of the seven caves modeled δ¹⁸O values of drip water and speleothem calcite are in good agreement with observed values. The mismatch of the remaining caves might be caused by the complexity of the cave system, beyond the parameterizations included in our cave model.

We then examine the response of the cave system to mid-Holocene (6000 yr before present, 6 ka climate conditions by forcing the ODSM with ECHAM5-wiso results from 6 ka simulations. For a set of twelve European caves, we compare the modeled mid-Holocene-to-modern difference in speleothem calcite δ¹⁸O to available measurements. We show that the general European changes are simulated well. However, local discrepancies are found, and might be explained either by a too low model resolution, complex local soil-atmosphere interactions affecting evapotranspiration or by cave specific factors

The Role of Chromohalobacter on Transport of Lanthanides and Cesium in the Dolomite Mineral System

Energy Technology Data Exchange (ETDEWEB)

Zengotita, Frances [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Emerson, Hilary Palmer [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Dittrich, Timothy M. [Wayne State Univ., Detroit, MI (United States); Swanson, Juliet S. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Reed, Donald T. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2017-12-01

The chemical behavior of actinide series elements and fission products is a concern for the Waste Isolation Pilot Plant repository due to their uncertain mobility in the subsurface salt formation. In this work, we are observing the behavior of the halophilic bacterium, Chromohalobacter, and its effect on the mobility of lanthanides and cesium in the presence of dolomite. Batch and minicolumn experiments were conducted with Cs⁺ and lanthanides (Nd³⁺, Eu³⁺) to quantify potential transport with bacteria. Preliminary results show that Cs does not interact strongly with dolomite or Chromohalobacter, while the lanthanides can interact strongly with both minerals and bacteria depending on which the Ln contacts first.

Comparison of the diagenetic and reservoir quality evolution between the anticline crest and flank of an Upper Jurassic carbonate gas reservoir, Abu Dhabi, United Arab Emirates

Science.gov (United States)

Morad, Daniel; Nader, Fadi H.; Gasparrini, Marta; Morad, Sadoon; Rossi, Carlos; Marchionda, Elisabetta; Al Darmaki, Fatima; Martines, Marco; Hellevang, Helge

2018-05-01

This petrographic, stable isotopic and fluid inclusion microthermometric study of the Upper Jurassic limestones of an onshore field, Abu Dhabi, United Arab Emirates (UAE) compares diagenesis in flanks and crest of the anticline. The results revealed that the diagenetic and related reservoir quality evolution occurred during three phases, including: (i) eogenesis to mesogenesis 1, during which reservoir quality across the field was either deteriorated or preserved by calcite cementation presumably derived from marine or evolved marine pore waters. Improvement of reservoir quality was due to the formation of micropores by micritization of allochems and creation of moldic/intragranular pores by dissolution of peloids and skeletal fragments. (ii) Obduction of Oman ophiolites and formation of the anticline of the studied field was accompanied by cementation by saddle dolomite and blocky calcite. High homogenization temperatures (125-175 °C) and high salinity (19-26 wt% NaCl eq) of the fluid inclusions, negative δ18OVPDB values (-7.7 to -2.9‰), saddle shape of dolomite, and the presence of exotic cements (i.e. fluorite and sphalerite) suggest that these carbonates were formed by flux of hot basinal brines, probably related to this tectonic compression event. (iii) Mesogenesis 2 during subsidence subsequent to the obduction event, which resulted in extensive stylolitization and cementation by calcite. This calcite cement occluded most of the remaining moldic and inter-/intragranular pores of the flank limestones (water zone) whereas porosity was preserved in the crest. This study contributes to: (1) our understanding of differences in the impact of diagenesis on reservoir quality evolution in flanks and crests of anticlines, i.e. impact of hydrocarbon emplacement on diagenesis, and (2) relating various diagenetic processes to burial history and tectonic events of foreland basins in the Arabian Gulf area and elsewhere.

Reaction Sintering of Mexican Dolomite – Zircon Mixtures

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Rodríguez-Galicia, J. L.

2005-08-01

Full Text Available The present work has been conducted aiming to develop additional phase [Ca3SiO5, Ca2SiO4 and/or Ca3Mg(SiO42]-bonded magnesia refractory materials via reaction sintering of dolomite-zircon mixtures, employing a Mexican dolomite containing an excess of 3 wt% of CaCO3. The study was based on phase equilibrium data extracted from the quaternary system CaO – MgO – SiO2 – ZrO2, to put it more precisely, base on the projection from the MgO-apex of the liquidus surface of the primary crystallization volume of MgO onto the opposite face of the above mentioned quaternary system. The refractory materials designed within this system were obtained by attrition milling, followed by cold isostatic pressing and high temperature reaction sintering. All initial and produced materials were characterized by ICP-AES, XRF, XRD, SEM-EDX, DTA and TG analyses. The results obtained indicated that reaction sintering of dolomite-zircon mixtures is an interesting route to produce MgO-CaZrO3-additional phase refractory materials.

El propósito de este trabajo ha sido obtener materiales refractarios de magnesia, aglomerados con una fase adicional [Ca3SiO5, Ca2SiO4 y/o Ca3Mg(SiO42], mediante la sinterización reactiva de mezclas de dolomita-circón, empleando para ello una dolomita mexicana que contiene un exceso de 3% en peso de CaCO3. El estudio se basa en la información relativa al equilibrio de fases del sistema CaO – MgO – SiO2 – ZrO2. En concreto se usa la proyección, desde el vértice del MgO, de la superficie de liquidus del volumen de cristalización primaria de este, hacia la cara opuesta de sistema cuaternario. Los materiales refractarios diseñados se han obtenido por molienda de atrición, seguida de un prensado isostático en frío y sinterización reactiva a alta temperatura. Todos los materiales, iniciales y finales, han sido caracterizados mediante ICPAES, FRX, DRX, MEB-EDX, ATD y TG. Los resultados obtenidos indican que la sinterizaci

Identification of spectrally similar materials using the USGS Tetracorder algorithm: The calcite-epidote-chlorite problem

Science.gov (United States)

Dalton, J.B.; Bove, D.J.; Mladinich, C.S.; Rockwell, B.W.

2004-01-01

A scheme to discriminate and identify materials having overlapping spectral absorption features has been developed and tested based on the U.S. Geological Survey (USGS) Tetracorder system. The scheme has been applied to remotely sensed imaging spectroscopy data acquired by the Airborne Visible and Infrared Imaging Spectrometer (AVIRIS) instrument. This approach was used to identify the minerals calcite, epidote, and chlorite in the upper Animas River watershed, Colorado. The study was motivated by the need to characterize the distribution of calcite in the watershed and assess its acid-neutralizing potential with regard to acidic mine drainage. Identification of these three minerals is difficult because their diagnostic spectral features are all centered at 2.3 ??m, and have similar shapes and widths. Previous studies overestimated calcite abundance as a result of these spectral overlaps. The use of a reference library containing synthetic mixtures of the three minerals in varying proportions was found to simplify the task of identifying these minerals when used in conjunction with a rule-based expert system. Some inaccuracies in the mineral distribution maps remain, however, due to the influence of a fourth spectral component, sericite, which exhibits spectral absorption features at 2.2 and 2.4 ??m that overlap the 2.3-??m absorption features of the other three minerals. Whereas the endmember minerals calcite, epidote, chlorite, and sericite can be identified by the method presented here, discrepancies occur in areas where all four occur together as intimate mixtures. It is expected that future work will be able to reduce these discrepancies by including reference mixtures containing sericite. ?? 2004 Elsevier Inc. All rights reserved.

Low temperature geothermal systems in carbonate-evaporitic rocks: Mineral equilibria assumptions and geothermometrical calculations. Insights from the Arnedillo thermal waters (Spain).

Science.gov (United States)

Blasco, Mónica; Gimeno, María J; Auqué, Luis F

2018-02-15

Geothermometrical calculations in low-medium temperature geothermal systems hosted in carbonate-evaporitic rocks are complicated because 1) some of the classical chemical geothermometers are, usually, inadequate (since they were developed for higher temperature systems with different mineral-water equilibria at depth) and 2) the chemical geothermometers calibrated for these systems (based on the Ca and Mg or SO 4 and F contents) are not free of problems either. The case study of the Arnedillo thermal system, a carbonate-evaporitic system of low temperature, will be used to deal with these problems through the combination of several geothermometrical techniques (chemical and isotopic geothermometers and geochemical modelling). The reservoir temperature of the Arnedillo geothermal system has been established to be in the range of 87±13°C being the waters in equilibrium with respect to calcite, dolomite, anhydrite, quartz, albite, K-feldspar and other aluminosilicates. Anhydrite and quartz equilibria are highly reliable to stablish the reservoir temperature. Additionally, the anhydrite equilibrium explains the coherent results obtained with the δ 18 O anhydrite - water geothermometer. The equilibrium with respect to feldspars and other aluminosilicates is unusual in carbonate-evaporitic systems and it is probably related to the presence of detrital material in the aquifer. The identification of the expected equilibria with calcite and dolomite presents an interesting problem associated to dolomite. Variable order degrees of dolomite can be found in natural systems and this fact affects the associated equilibrium temperature in the geothermometrical modelling and also the results from the Ca-Mg geothermometer. To avoid this uncertainty, the order degree of the dolomite present in the Arnedillo reservoir has been determined and the results indicate 18.4% of ordered dolomite and 81.6% of disordered dolomite. Overall, the results suggest that this multi

Selective Separation of Fluorite, Barite and Calcite with Valonea Extract and Sodium Fluosilicate as Depressants

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Zijie Ren

2017-02-01

Full Text Available Fluorite, barite and calcite are important industry minerals. However, they often co-exist, presenting difficulty in selectively separating them due to their similar surface properties. In this study, valonea extract and sodium fluosilicate were used as depressants to selectively separate them by flotation, with sodium oleate as the collector. The single mineral flotation results showed that valonea extract displayed the strongest depression on calcite, while sodium fluosilicate displayed the strongest depression on barite. These two depressants allowed selective separation of the three minerals through sequential flotation. The flotation of mixed minerals showed that 94% of the calcite was successfully depressed by the valonea extract, and 95% recovery of the fluorite was achieved in the subsequent flotation with sodium fluosilicate depressing barite. The different depressant–mineral interactions were investigated via electro-kinetic studies and molecular dynamics (MD simulations using the Materials Studio 6.0 program. The valonea extract exhibited the strongest adsorption on the calcite surface, and sodium fluosilicate exhibited the strongest adsorption on the barite surface, which prevented oleate species from reacting with Ca2+ or Ba2+ surface sites. This study provides useful guidance for how to process fluorite, barite and calcite resources.

Immobilization of nanoparticles by occlusion into microbial calcite

DEFF Research Database (Denmark)

Skuce, Rebecca L.; Tobler, Dominique Jeanette; MacLaren, Ian

2017-01-01

systems. In this study, the ureolytic bacteria Sporosarcina pasteurii was used to induce calcium carbonate precipitation in the presence of organo-metallic manufactured nanoparticles. As calcite crystals grew the nanoparticles in the solution became trapped inside these crystals. Capture of NPs within...

The effect of dolomite type and Al2O3 content on the phase composition in aluminous cements containing spinel

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R. Naghizadeh

2011-06-01

Full Text Available In this paper, the effect of dolomite type and Al2O3 content on the phase composition in aluminous cements containing MA spinel is investigated. For this reason, the raw and calcined dolomites are used as raw materials along with calcined alumina in the preparation of the cement. Then, different compositions are prepared at 1350°C using the sintering method and their mineralogical compositions are investigated using the diffractometric technique. Also, their microstructures arre evaluated. The results indicate that raw materials used have great effect on the type and amount of formed phases in cement composition. Independently of the dolomite type used, a mixed phase product consisting of spinel accompanied by CA and CA2 is obtained. The content of CA phase in the cement composition is decreased with increasing of Al2O3 in the raw materials composition. On the other hand, the content of CA2 phase is increased with the addition of Al2O3. In addition, the results show that the formation of C12A7 is favored by use of calcined dolomite.

Lower Cretaceous Puez key-section in the Dolomites - towards the mid-Cretaceous super-greenhouse

Science.gov (United States)

Lukeneder, A.; Halásová, E.; Rehákova, D.; Józsa, Š.; Soták, J.; Kroh, A.; Jovane, L.; Florindo, F.; Sprovieri, M.; Giorgioni, M.; Lukeneder, S.

2012-04-01

Investigations on different fossil groups in addition to isotopic, paleomagnetic and geochemical analysis are combined to extract the Early Cretaceous history of environmental changes, as displayed by the sea level and climate changes. Results on biostratigraphy are integrated with other dating methods as magnetostraigraphy, correlation and cyclostratigraphy. The main investigation topics of the submitted project within the above-described framework are the biostratigraphic (Lukeneder and Aspmair, 2006, 2012), palaeoecological (Lukeneder, 2008, 2012), palaeobiogeographic, lithostratigraphic (Lukeneder, 2010, 2011), cyclostratigraphic and magnetostratigraphic development of the Early Cretaceous in the Puez area. The main sections occur in expanded outcrops located on the southern margin of the Puez Plateau, within the area of the Puez-Geisler Natural Park, in the northern part of the Dolomites (South Tyrol, North Italy). The cephalopod, microfossil and nannofossil faunas and floras from the marly limestones to marls here indicates Hauterivian to Albian/Cenomanian age. Oxygen isotope values from the Lower Cretaceous Puez Formation show a decreasing trend throughout the log, from -1.5‰ in the Hauterivian to -4.5‰ in the Albian/Cenomanian. The decreasing values mirror an increasing trend in palaeotemperatures from ~ 15-18°C in the Hauterivian up to ~25-30 °C in the Albian/Cenomanian. The trend probably indicates the positive shift in temperature induced by the well known Mid Cretaceous Ocean warming (e.g., Super-Greenhouse). The cooperative project (FWF project P20018-N10; 22 international scientists): An integrative high resolution project. Macro- and microfossils, isotopes, litho-, cyclo-, magneto-and biostratigraphy as tools for investigating the Lower Cretaceous within the Dolomites (Southern Alps, Northern Italy) -The Puez area as a new key region of the Tethyan Realm), is on the way since 2008 by the Natural History Museum in Vienna and the 'Naturmuseum S�

Development of Miocene-Pliocene reef trend, St. Croix, U. S. Virgin Islands

Energy Technology Data Exchange (ETDEWEB)

Gill, I.; Eby, D.E.; Hubbard, D.K.; Frost, S.H.

1988-01-01

The Miocene-Pliocene reef trend on St. Croix, U.S. Virgin Islands, rims the present southern western coasts of the island and includes accompanying lagoonal and forereef facies. The reef trend was established on a foram-algal bank facies that represents basinal shallowing from the deep-water pelagic and hemipelagic facies of the Miocene Kingshill Limestone. Information on facies distribution and thickness is derived from rock exposures and 22 test wells drilled to a maximum depth of 91 m. The greatest thickness of the reef facies exists in a subsidiary graben on the south coast of St. Croix. The thickness of the reef section in this locality is due to preservation of the section in a downdropped block. Reef faunas include extant corals, as well as several extinct genera. Extant corals (e.g. Montastrea annularis, Diploria sp., and Porites porites) and extinct corals (e.g., Stylophora affinis, Antillea bilobata, and Thysanus sp.) are the main reef frame-builders. Coralline algea and large benthic foraminifera are significant contributors to the sediments both prior to and during scleractinian reef growth. Dolomitization and calcite cementation occur prominantly in an area corresponding to a Holocene lagoon. The spatial distribution of the dolomite suggests that the lagoon is a Tertiary feature directly related to the dolomitization process. Stable isotopic values suggest dolomitization of fluids of elevated salinity.

THE ANISIAN MACROFLORA FROM THE NORTHERN DOLOMITES (KÜHWIESENKOPF/ MONTE PRÀ DELLA VACCA, BRAIES: A FIRST REPORT

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CARMEN BROGLIO LORIGA

2002-11-01

Full Text Available The knowledge of Triassic macroflora from the Dolomites mostly concerns the Ladinian, while literature data on Anisian plants are scarce. This gap is filled by the discovery, reported here, of a rich plant deposit from Kühwiesenkopf / Monte Prà della Vacca (Prags/Braies Dolomites. The fossils occur in a horizon, about 1 m thick, from the lower part of the Dont Formation, a basinal unit mostly constituted by hemipelagic, terrigenous-carbonatic sediments of Pelsonian - Illyrian age. The stratigrafic interval with the plant horizon is Pelsonian in age. A preliminary systematic analysis of the numerous and well preserved specimens has allowed the identification of at least 17 genera. The taxa belong primarily to the Pteridophyta (Anomopteris, Neuropteridium, Cladophlebis, Crematopteris, ?Marattiopsis, subordinately to the Cycadophyta (Bjuvia, Taeniopteris, Dioonitocarpidium, Pterophyllum / Nilssonia. Coniferophyta are represented by Voltzia, ?Voltzia and Albertia; the latter genus is recorded herein for the first time in the Middle Triassic of the Dolomites. Besides, two Lycophyta genera (?Isoetites, Lycophyta new taxon, three Pteridospermae genera (?Sagenopteris, Scytophyllum and Peltaspermum, and one Sphenophyta genus (Equisetites have also been recognized.   

Crystallization of ikaite and its pseudomorphic transformation into calcite: Raman spectroscopy evidence

Science.gov (United States)

Sánchez-Pastor, N.; Oehlerich, Markus; Astilleros, José Manuel; Kaliwoda, Melanie; Mayr, Christoph C.; Fernández-Díaz, Lurdes; Schmahl, Wolfgang W.

2016-02-01

Ikaite (CaCO3·6H2O) is a metastable phase that crystallizes in nature from alkaline waters with high phosphate concentrations at temperatures close to 0 °C. This mineral transforms into anhydrous calcium carbonate polymorphs when temperatures rise or when exposed to atmospheric conditions. During the transformation in some cases the shape of the original ikaite crystal is preserved as a pseudomorph. Pseudomorphs after ikaite are considered as a valuable paleoclimatic indicator. In this work we conducted ikaite crystal growth experiments at near-freezing temperatures using the single diffusion silica gel technique, prepared with a natural aqueous solution from the polymictic lake Laguna Potrok Aike (51°57‧S, 70°23‧W) in Patagonia, Argentina. The ikaite crystals were recovered from the gels and the transformation reactions were monitored by in situ Raman spectroscopy at two different temperatures. The first spectra collected showed the characteristic features of ikaite. In successive spectra new bands at 1072, 1081 and 1086 cm-1 and changes in the intensity of bands corresponding to the OH modes were observed. These changes in the Raman spectra were interpreted as corresponding to intermediate stages of the transformation of ikaite into calcite and/or vaterite. After a few hours, the characteristics of the Raman spectrum were consistent with those of calcite. While ikaite directly transforms into calcite at 10 °C in contact with air, at 20 °C this transformation involves the formation of intermediate, metastable vaterite. During the whole process the external shape of ikaite crystals was preserved. Therefore, this transformation showed the typical characteristics of a pseudomorphic mineral replacement, involving the generation of a large amount of porosity to account for the large difference in molar volumes between ikaite and calcite. A mechanism involving the coupled dissolution of ikaite and crystallization of calcite/vaterite is proposed for this

Tuning the wettability of calcite cubes by varying the sizes of the polystyrene nanoparticles attached to their surfaces

International Nuclear Information System (INIS)

He Yongjun; Li Tanliang; Yu Xiangyang; Zhao Shiyong; Lu Jianhua; He Jia

2007-01-01

The wettability of calcite cubes was tuned by varying the sizes of the polystyrene nanoparticles attached to their surfaces via a dispersion polymerization. The products were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersion spectrum (EDS) and Fourier transformation infrared spectrum (FTIR). The results showed that the hydrophobicity of the calcite cubes was enhanced with the increase of the size of the polystyrene nanoparticles attached. Using polystyrene nanoparticle-attached calcite cubes (PNACC) as emulsifiers, stable water-in-tricaprylin Pickering emulsions were produced. By gelling the water droplets of the Pickering emulsions, the hierarchical structures of polystyrene nanoparticle-attached calcite cube-armored microspheres were obtained. The polystyrene nanoparticle-attached calcite cubes were expected to have novel surface properties similar neither to traditional Pickering particles, nor to macroscopically asymmetrical Janus particles

Coccolith calcite time capsules preserve a molecule-specific record of pCO2

Science.gov (United States)

McClelland, H. L. O.; Pearson, A.; Hermoso, M.; Wilkes, E.; Lee, R. B. Y.; Rickaby, R. E. M.

2017-12-01

Coccolithophores are single-celled phytoplankton that have contributed organic matter and calcite to marine sediments since the Late Triassic. The carbon isotopic compositions of both the calcite, and the organic matter, constitute valuable archives of information about the interaction between these organisms and the environments in which they lived. The isotopic composition of alkenone lipids, a recalcitrant component of coccolithophore organic carbon produced by a single family of coccolithophores, has been widely used to reconstruct pCO2 in the geological past. However, the robustness of this approach has remained controversial, due in part to the difficulties associated with reproducing pCO2 changes across periods of known pCO2 change, and uncertainties in relevant physiological variables such as growth rate and cell size. Meanwhile the calcite, produced in the form of plates called coccoliths, and which has had limited utility in paleoclimate reconstructions due to its large and variable departures from the isotopic composition of abiogenic calcite, has garnered increasing attention in recent years for the environmental and physiological information it contains. Here we show that polysaccharides preserved within the calcite crystal lattice of near monospecific fractions of fossil coccoliths constitute an ancient pristine source of organic carbon that unlike alkenones is unambiguously associated with the coccolith1. The isotopic composition of these polysaccharides, in tandem with that of the host coccolith calcite, and morphometrics from the same coccoliths2, can be used simultaneously constrain a recently published cellular carbon isotope flux model3, embedded in a more complex nutrient limitation model, in a powerful new approach to simultaneously predict cellular parameters and pCO2. We demonstrate the validity of this approach across a glacial / interglacial cycle. Lee, R. B. Y., et al,, Nat. Commun. 7, 13144 (2016). McClelland, H. L. O. et al. Sci. Rep. 6

Light rare earth element systematics as a tool for investigating the petrogenesis of phoscorite-carbonatite associations, as exemplified by the Phalaborwa Complex, South Africa

Science.gov (United States)

Milani, Lorenzo; Bolhar, Robert; Frei, Dirk; Harlov, Daniel E.; Samuel, Vinod O.

2017-12-01

In-situ trace element analyses of fluorapatite, calcite, dolomite, olivine, and phlogopite have been undertaken on representative phoscorite and carbonatite rocks of the Palaeoproterozoic Phalaborwa Complex. Textural and compositional characterization reveals uniformity of fluorapatite and calcite among most of the intrusions, and seems to favor a common genetic origin for the phoscorite-carbonatite association. Representing major repositories for rare earth elements (REE), fluorapatite and calcite exhibit tightly correlated light REE (LREE) abundances, suggesting that partitioning of LREE into these rock forming minerals was principally controlled by simple igneous differentiation. However, light rare earth element distribution in apatite and calcite cannot be adequately explained by equilibrium and fractional crystallization and instead favors a complex crystallization history involving mixing of compositionally distinct magma batches, in agreement with previously reported mineral isotope variability that requires open-system behaviour.

On the origin of calcite-cemented sandstones in the clearwater formation oil-sands, Alberta

Energy Technology Data Exchange (ETDEWEB)

Colquhoun, I.M.

1999-01-01

This thesis examined the formation of calcite-cemented sandstones in the Clearwater Formation within the Cold Lake and southern Primrose areas of the Alberta oil sands. Three stages of diagenesis have been recognized, both in the calcite-cemented sandstones and reservoir sands. Diagenesis of the Clearwater Formation in the Cold Lake and southern Primrose areas ended once the reservoir filled with hydrocarbons, but in the Cold Lake area, diagenesis of water-saturated sands likely continued after hydrocarbon emplacement. The reservoir sands in the formation contain a diverse clay mineral assemblage. In general, 0.7 nm clays dominate the diagenetic clay mineralogy of the Clearwater sands. Reservoir sands that contain large amounts of detrital clays and early diagenetic, grain-coating chlorite/smectite have significantly reduced bitumen-saturation. The presence of detrital and diagenetic smectitic clays complicates the removal of bitumen from the Clearwater formation using cyclic steam stimulation techniques because they swell during steam stimulation and reduce porosity and permeability of reservoir sands. Reservoir sands that contain kaolinite, feldspar and calcite react to form smectitic clays, which swell upon cyclic steam stimulation and further reduce porosity and permeability of reservoir sands. However, in the Cold Lake and Primrose areas, the dominant clay mineral is berthierine, which is associated with high calcite, which help to preserve porosity, permeability and bitumen saturation. The porous nature of bitumen-saturated, calcite-cemented sandstones that are laterally extensive could possibly provide a preferential path for steam to initiate calcite dissolution and produce significant concentrations of dissolved carbon dioxide in injected fluids. It was noted that this may then precipitate as carbonate scale within the reservoir and could cause formation damage or affect production equipment. 207 refs., 9 tabs., 58 figs., 3 appendices.

Unravelling the enigmatic origin of calcitic nanofibres in soils and caves: purely physicochemical or biogenic processes?

Science.gov (United States)

Bindschedler, S.; Cailleau, G.; Braissant, O.; Millière, L.; Job, D.; Verrecchia, E. P.

2014-05-01

Calcitic nanofibres are ubiquitous habits of secondary calcium carbonate (CaCO3) accumulations observed in calcareous vadose environments. Despite their widespread occurrence, the origin of these nanofeatures remains enigmatic. Three possible mechanisms fuel the debate: (i) purely physicochemical processes, (ii) mineralization of rod-shaped bacteria, and (iii) crystal precipitation on organic templates. Nanofibres can be either mineral (calcitic) or organic in nature. They are very often observed in association with needle fibre calcite (NFC), another typical secondary CaCO3 habit in terrestrial environments. This association has contributed to some confusion between both habits, however they are truly two distinct calcitic features and their recurrent association is likely to be an important fact to help understanding the origin of nanofibres. In this paper the different hypotheses that currently exist to explain the origin of calcitic nanofibres are critically reviewed. In addition to this, a new hypothesis for the origin of nanofibres is proposed based on the fact that current knowledge attributes a fungal origin to NFC. As this feature and nanofibres are recurrently observed together, a possible fungal origin for nanofibres which are associated with NFC is investigated. Sequential enzymatic digestion of the fungal cell wall of selected fungal species demonstrates that the fungal cell wall can be a source of organic nanofibres. The obtained organic nanofibres show a striking morphological resemblance when compared to their natural counterparts, emphasizing a fungal origin for part of the organic nanofibres observed in association with NFC. It is further hypothesized that these organic nanofibres may act as templates for calcite nucleation in a biologically influenced mineralization process, generating calcitic nanofibres. This highlights the possible involvement of fungi in CaCO3 biomineralization processes, a role still poorly documented. Moreover, on a global

Time scales for dissolution of calcite fracture fillings and implications for saturated zone radionuclide transport at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Winterle, J.R.; Murphy, W.M.

1999-01-01

An analysis was performed to estimate time scales for dissolution of calcite fracture fillings in the fractured tuff aquifer that underlies Yucca Mountain (YM), Nevada, where groundwater is chemically undersaturated with respect to calcite. The impetus for this analysis originates from speculation that undissolved calcite in the saturated zone is evidence for limited diffusive exchange between fracture and matrix waters. Assuming that matrix diffusion is the rate-limiting process, the time scale for dissolution of calcite fracture fillings depends on the amount of calcite initially deposited, the distance between flowing fractures, the degree of chemical disequilibrium, and the rate of diffusion. Assuming geochemistry of J-13 well water in free-flowing fractures, estimated time scales for complete dissolution of matrix-entrapped calcite range from about 10 4 yr for a 2 mm-thick deposit located 1 m from a flowing fracture, to over 10 7 yr for a 2 cm-thick deposit located 100 m from a flowing fracture. The authors conclude that, given the geochemical and hydrologic characteristics observed at YM, the persistence of calcite minerals over geologic time scales in aquifers where flowing water is under-saturated with calcite does not necessarily preclude matrix diffusion as a dilution mechanism. However, the model suggests that the effective spacing between flowing fractures may be large enough to diminish the overall benefit of matrix diffusion to proposed high-level waste repository performance

The influence of mineralization on the phase composition and properties of low-burned clay-dolomited composition materials

International Nuclear Information System (INIS)

Shirin-zade, I.N.; Ganbarov, D.M.

2008-01-01

With aim of acceleration of dissociation of carbonates in clay-dolomited compositions Na 2 SiF 6 was added. Addition mineralization raise stability of composition reaches 20-30 MPa. Na 2 SiF 6 mineralization makes more active decomposition of dolomite and accelerate appearance of new creations. It was experimentally proved that adding of mineralization of Na 2 SiF 6 promote to appearance in mixture of intermediate double salts which are bring down temperature of dissociation of carbonates. Accelerated action of mineralization Na 2 SiF 6 accepted by x-ray, DTA and x-ray spectroscopy

Adsorption of polar aromatic hydrocarbons on synthetic calcite

DEFF Research Database (Denmark)

Madsen, Lene; Grahl-Madsen, Laila; Grøn, Christian

1996-01-01

The wettability of hydrocarbon reservoirs depends on how and to what extent the organic compounds are adsorbed onto the surfaces of calcite, quartz and clay. A model system of synthetic call cite, cyclohexane and the three probe molecules: benzoic acid, benzyl alcohol and benzylamine, have been...

Effect of dolomite and biochar addition on N2O and CO2 emissions from acidic tea field soil.

Science.gov (United States)

Oo, Aung Zaw; Sudo, Shigeto; Akiyama, Hiroko; Win, Khin Thuzar; Shibata, Akira; Yamamoto, Akinori; Sano, Tomohito; Hirono, Yuhei

2018-01-01

A laboratory study was conducted to study the effects of liming and different biochar amendments on N2O and CO2 emissions from acidic tea field soil. The first experiment was done with three different rates of N treatment; N 300 (300 kg N ha-1), N 600 (600 kg N ha-1) and N 900 (900 kg N ha-1) and four different rates of bamboo biochar amendment; 0%, 0.5%, 1% and 2% biochar. The second experiment was done with three different biochars at a rate of 2% (rice husk, sawdust, and bamboo) and a control and lime treatment (dolomite) and control at two moisture levels (50% and 90% water filled pore space (WFPS)). The results showed that dolomite and biochar amendment significantly increased soil pH. However, only biochar amendment showed a significant increase in total carbon (C), C/N (the ratio of total carbon and total nitrogen), and C/IN ratio (the ratio of total carbon and inorganic nitrogen) at the end of incubation. Reduction in soil NO3--N concentration was observed under different biochar amendments. Bamboo biochar with the rates of 0.5, 1 and 2% reduced cumulative N2O emission by 38%, 48% and 61%, respectively, compare to the control soil in experiment 1. Dolomite and biochar, either alone or combined significantly reduced cumulative N2O emission by 4.6% to 32.7% in experiment 2. Reduction in N2O production under biochar amendment was due to increases in soil pH and decreases in the magnitude of mineral-N in soil. Although, both dolomite and biochar increased cumulative CO2 emission, only biochar amendment had a significant effect. The present study suggests that application of dolomite and biochar to acidic tea field soil can mitigate N2O emissions.

New explanation for extreme u-234 u-238 disequilibria in a dolomitic aquifer

CSIR Research Space (South Africa)

Kronfeld, J

1994-05-01

Full Text Available High U-234/U-238 activity ratios are found in the shallow groundwater of the phreatic Transvaal Dolomite Aquifer. The aquifer is uranium poor, while the waters are oxygen rich and young. Tritium and C-14 are used to show that the disequilibrium...

Journal of Agriculture, Science and Technology - Vol 10, No 2 (2008)

African Journals Online (AJOL)

The effect of liming an acid nitisol with with either calcite of dolomite on two common bean ( Phaseolus vulgaris L.) varieties differing in aluminium tolerance · EMAIL FULL TEXT EMAIL FULL TEXT · DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT. EN Mugai, SG Agong, H Matsumoto ...

Interface waves propagating along tensile fractures in dolomite

International Nuclear Information System (INIS)

Roy, S.; Pyrak-Nolte, L.J.

1995-01-01

Elastic interface waves have been observed in induced tensile fractures in dolomite rock cores. Multiscaling wavelet analysis distinguishes the interface wave from bulk shear waves, quantifies the interface wave spectral content, and determines the arrival time of peak energy. The dominant seismic energy is concentrated in the slow interface wave, with little or no detectable energy in the fast wave. As stress across the fracture increases, the slow interface wave velocity increases, and the frequency of the spectral peak shifts to higher frequencies. The shear dynamic specific stiffness of the fracture was calculated from the peak energy arrival time as a function of stress. 13 refs., 5 figs., 1 tab

Petrophysical characterization of the Dolomitic Member of the Boñar Formation (Upper Cretaceous; Duero Basin, Spain) as a potential CO2 reservoir

Energy Technology Data Exchange (ETDEWEB)

Suarez-Gonzalez, A.; Kovacs, C.; Herrero-Hernandez, A.; Gomez-Fernandez, F.

2016-07-01

Boñar Formation (Upper Cretaceous) is a mainly carbonate succession, which outcrops in the North of Duero Basin (Spain). According to the existing data, the Dolomitic Member of this formation appears to be the most suitable for geological storage of CO2. The main objective of this study is to find evidence to support, clarify and specify –at an initial level– the potential of the Dolomitic Member of the Boñar Formation as a geological reservoir. The study covers density, porosity and permeability tests on samples obtained from the outcrop of the succession near the village of Boñar (León). According to the analysis and interpretation of the mentioned petrophysical properties, the porosity of the Dolomitic Member is within the acceptable range for CO2 geological storage, but the permeability values are far too low. This minimizes the possibilities of the Dolomitic Member –and probably of the whole Boñar Formation– to become an appropriate CO2 reservoir. (Author)

Viruses Occur Incorporated in Biogenic High-Mg Calcite from Hypersaline Microbial Mats

Science.gov (United States)

De Wit, Rutger; Gautret, Pascale; Bettarel, Yvan; Roques, Cécile; Marlière, Christian; Ramonda, Michel; Nguyen Thanh, Thuy; Tran Quang, Huy; Bouvier, Thierry

2015-01-01

Using three different microscopy techniques (epifluorescence, electronic and atomic force microscopy), we showed that high-Mg calcite grains in calcifying microbial mats from the hypersaline lake “La Salada de Chiprana”, Spain, contain viruses with a diameter of 50–80 nm. Energy-dispersive X-ray spectrometer analysis revealed that they contain nitrogen and phosphorus in a molar ratio of ~9, which is typical for viruses. Nucleic acid staining revealed that they contain DNA or RNA. As characteristic for hypersaline environments, the concentrations of free and attached viruses were high (>1010 viruses per g of mat). In addition, we showed that acid treatment (dissolution of calcite) resulted in release of viruses into suspension and estimated that there were ~15 × 109 viruses per g of calcite. We suggest that virus-mineral interactions are one of the possible ways for the formation of nano-sized structures often described as “nanobacteria” and that viruses may play a role in initiating calcification. PMID:26115121

Adsorption and migration of single metal atoms on the calcite (10.4) surface

International Nuclear Information System (INIS)

Pinto, H; Haapasilta, V; Lokhandwala, M; Foster, Adam S; Öberg, S

2017-01-01

Transition metal atoms are one of the key ingredients in the formation of functional 2D metal organic coordination networks. Additionally, the co-deposition of metal atoms can play an important role in anchoring the molecular structures to the surface at room temperature. To gain control of such processes requires the understanding of adsorption and diffusion properties of the different transition metals on the target surface. Here, we used density functional theory to investigate the adsorption of 3 d (Ti, Cr, Fe, Ni, Cu), 4 d (Zr, Nb, Mo, Pd, Ag) and 5 d (Hf, W, Ir, Pt, Au) transition metal adatoms on the insulating calcite (10.4) surface. We identified the most stable adsorption sites and calculated binding energies and corresponding ground state structures. We find that the preferential adsorption sites are the Ca–Ca bridge sites. Apart from the Cr, Mo, Cu, Ag and Au all the studied metals bind strongly to the calcite surface. The calculated migration barriers for the representative Ag and Fe atoms indicates that the metal adatoms are mobile on the calcite surface at room temperature. Bader analysis suggests that there is no significant charge transfer between the metal adatoms and the calcite surface. (paper)

Tuning hardness in calcite by incorporation of amino acids.

Science.gov (United States)

Kim, Yi-Yeoun; Carloni, Joseph D; Demarchi, Beatrice; Sparks, David; Reid, David G; Kunitake, Miki E; Tang, Chiu C; Duer, Melinda J; Freeman, Colin L; Pokroy, Boaz; Penkman, Kirsty; Harding, John H; Estroff, Lara A; Baker, Shefford P; Meldrum, Fiona C

2016-08-01

Structural biominerals are inorganic/organic composites that exhibit remarkable mechanical properties. However, the structure-property relationships of even the simplest building unit-mineral single crystals containing embedded macromolecules-remain poorly understood. Here, by means of a model biomineral made from calcite single crystals containing glycine (0-7 mol%) or aspartic acid (0-4 mol%), we elucidate the origin of the superior hardness of biogenic calcite. We analysed lattice distortions in these model crystals by using X-ray diffraction and molecular dynamics simulations, and by means of solid-state nuclear magnetic resonance show that the amino acids are incorporated as individual molecules. We also demonstrate that nanoindentation hardness increased with amino acid content, reaching values equivalent to their biogenic counterparts. A dislocation pinning model reveals that the enhanced hardness is determined by the force required to cut covalent bonds in the molecules.

Coccolithophore responses to environmental variability in the South China Sea: species composition and calcite content

Science.gov (United States)

Jin, Xiaobo; Liu, Chuanlian; Poulton, Alex J.; Dai, Minhan; Guo, Xianghui

2016-08-01

Coccolithophore contributions to the global marine carbon cycle are regulated by the calcite content of their scales (coccoliths) and the relative cellular levels of photosynthesis and calcification rates. All three of these factors vary between coccolithophore species and with response to the growth environment. Here, water samples were collected in the northern basin of the South China Sea (SCS) during summer 2014 in order to examine how environmental variability influenced species composition and cellular levels of calcite content. Average coccolithophore abundance and their calcite concentration in the water column were 11.82 cells mL-1 and 1508.3 pg C mL-1, respectively, during the cruise. Water samples can be divided into three floral groups according to their distinct coccolithophore communities. The vertical structure of the coccolithophore community in the water column was controlled by the trophic conditions, which were regulated by mesoscale eddies across the SCS basin. The evaluation of coccolithophore-based calcite in the surface ocean also showed that three key species in the SCS (Emiliania huxleyi, Gephyrocapsa oceanica, Florisphaera profunda) and other larger, numerically rare species made almost equal contributions to total coccolith-based calcite in the water column. For Emiliania huxleyi biometry measurements, coccolith size positively correlated with nutrients (nitrate, phosphate), and it is suggested that coccolith length is influenced by light and nutrients through the regulation of growth rates. Larger-sized coccoliths were also linked statistically to low pH and calcite saturation states; however, it is not a simple cause and effect relationship, as carbonate chemistry was strongly co-correlated with the other key environmental factors (nutrients, light).

Applying Transmission Kikuchi Diffraction (TKD) to Understand Nanogranular Fault Rock Materials

Science.gov (United States)

Smith, S. A. F.; Demurtas, M.; Prior, D. J.; Di Toro, G.

2017-12-01

Nanoparticles (transparent foils with resolutions that can be below 10 nm. Therefore, the potential of TKD to understand deformation processes in nanoparticles is very high. We present results of TKD analysis performed on mixed calcite-dolomite gouges deformed in a rotary-shear apparatus at slip rates ranging from sub-seismic to co-seismic (30 µm/s to 1 m/s). Samples for TKD were prepared by argon ion slicing, a method that yields relatively large (104 µm2) electron transparent areas, as well as standard argon ion milling. Coupled TKD-EDS analysis allows quantification of elemental contents at a scale of tens of nanometers. Preliminary results show that at a slip velocity of 1 m/s, the localized slip zone that forms in the gouges during shearing is composed of recrystallized grains of calcite and Mg-calcite (the latter being a decarbonation product of dolomite) with an average grain size of c. 300 nm. Individual grains are characterized by relatively straight boundaries, and many triple and quadruple grain junctions are present. The nanogranular aggregates show a polygonised texture with absence of clear porosity and shape preferred orientation. Orientation data show a random distribution of the calcite c-axes. Further investigation will help to obtain new insights into the deformation mechanisms active during seismic faulting in carbonate-bearing faults. The integration of grain size, grain shape and crystallographic information into flow laws will help to describe and predict the rheological behaviour of carbonate faults during seismic sliding.

Isostructural exclusion of elements between aragonite and calcite layers in the shell of the Pacific oyster Crassostrea gigas

International Nuclear Information System (INIS)

Markwitz, A.; Gauldie, R.W.; Trompetter, W.J.; Pithie, J.; Jamieson, D.N.; Sharma, S.K.

1999-01-01

Sections of the shell of the farmed Pacific oyster 'Crassostrea gigas' that are available commercially in Wellington, New Zealand, showed a distinct alternating pattern in the shell mineral when observed by reflected light. The layers were identified by Raman scattering as alternating bands of the calcite and aragonite mineral forms of calcium carbonate using the micro-Raman facility at the Hawaii Institute of Geophysics and Planetology. The differences in the unit cell structure of calcite and aragonite favour different trace elements in the two minerals. Aragonite is isostructural with Strontianite SrCO 3 , and calcite is isostructural with Smithsonite ZnCO 3 . As a result, Sr deposition should be favoured in the aragonite layer and is excluded from the calcite layer; and, conversely, Zn deposition should be favoured in the calcite layer and is excluded from the aragonite layer. However, up to today, significant differences in the pattern of Sr and Zn in microprobe scans are not discovered. By ion microprobe analysis, it was shown that differences in the unit cell structure of calcite and aragonite favor different trace elements in the two minerals

Microstratigraphic logging of calcite fabrics in speleothems as tool for palaeoclimate studies

Directory of Open Access Journals (Sweden)

Silvia Frisia

2015-01-01

Full Text Available The systematic documentation of calcite fabrics in stalagmites and flowstones provides robustness to palaeoclimate interpretation based on geochemical proxies, but it has been neglected because it is difficult to transform crystal morphologies into numerical values, and construct fabric time series. Here, general criteria that allow for coding fabrics of calcite composing stalagmites and flowstones is provided. Being based on known models of fabric development, the coding ascribes sequential numbers to each fabric, which reflect climate-related parameters, such as changes in drip rate variability, bio-mediation or diagenetic modifications. Acronyms are proposed for Columnar types, Dendritic, Micrite, Microsparite and Mosaic fabrics, whose use could then render possible comparison of calcite fabrics in stalagmites and flowstones from diverse latitudinal and altitudinal settings. The climatic and environmental significance of similarities in the geochemical signals and trends analysed in coeval stalagmites and flowstones (or differences in the signals and trends will be more robust when compared with fabric time series. This is particularly true where, such as in the Holocene, changes in geochemical values may be subtle, yet fabrics may show changes related to variations in supersaturation, drip rate or input of detrital particles or organic compounds. The proposed microstratigraphic logging allows recognition of changes in stable isotope ratio or trace element values that can be ascribed to hydrology and diagenesis, with considerable improvement of reconstructions based on the chemical proxies of stalagmites and flowstones composed of calcite.

Spectroscopic characterization of Greek dolomitic marble surface interacted with uranium and thorium in aqueous solutions

International Nuclear Information System (INIS)

Godelitsas, A.; Kokkoris, M.; Chatzitheodoridis, E.; Misaelides, P.

2008-01-01

The surface of a typical Greek (Thassian) dolomitic marble was studied after interaction with U- and Th-containing aqueous solutions (1000 mg/L, free-drift experiments for 1 week at atmospheric P CO 2 ), using 12 C-RBS and Laser μ-Raman spectroscopy. Powder-XRD and SEM-EDS were also applied to investigate the phases deposited on the surface of the interacted samples. The obtained results indicated a considerable removal of U from the aqueous medium mainly due to massive surface precipitation of amorphous UO 2 -hydroxide phases forming a relatively thick (μm-sized) coating on the carbonate substrate. The interaction of Th with dolomitic marble surface is also intense leading to a formation of an amorphous Th-hydroxide layer of similar thickness but of significantly lower elemental atomic proportion

Spectroscopic characterization of Greek dolomitic marble surface interacted with uranium and thorium in aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Godelitsas, A. [Faculty of Geology and Geoenvironment, University of Athens, 15784 Zographou, Athens (Greece)], E-mail: agodel@geol.uoa.gr; Kokkoris, M. [School of Applied Mathematics and Physics, National Technical University of Athens, 15780 Zographou, Athens (Greece); Chatzitheodoridis, E. [School of Mining and Metallurgical Engineering, National Technical University of Athens, 15780 Zographou, Athens (Greece); Misaelides, P. [Faculty of Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki (Greece)

2008-05-15

The surface of a typical Greek (Thassian) dolomitic marble was studied after interaction with U- and Th-containing aqueous solutions (1000 mg/L, free-drift experiments for 1 week at atmospheric P{sub CO{sub 2}}), using {sup 12}C-RBS and Laser {mu}-Raman spectroscopy. Powder-XRD and SEM-EDS were also applied to investigate the phases deposited on the surface of the interacted samples. The obtained results indicated a considerable removal of U from the aqueous medium mainly due to massive surface precipitation of amorphous UO{sub 2}-hydroxide phases forming a relatively thick ({mu}m-sized) coating on the carbonate substrate. The interaction of Th with dolomitic marble surface is also intense leading to a formation of an amorphous Th-hydroxide layer of similar thickness but of significantly lower elemental atomic proportion.

Spectroscopic characterization of Greek dolomitic marble surface interacted with uranium and thorium in aqueous solutions

Science.gov (United States)

Godelitsas, A.; Kokkoris, M.; Chatzitheodoridis, E.; Misaelides, P.

2008-05-01

The surface of a typical Greek (Thassian) dolomitic marble was studied after interaction with U- and Th-containing aqueous solutions (1000 mg/L, free-drift experiments for 1 week at atmospheric PCO2), using 12C-RBS and Laser μ-Raman spectroscopy. Powder-XRD and SEM-EDS were also applied to investigate the phases deposited on the surface of the interacted samples. The obtained results indicated a considerable removal of U from the aqueous medium mainly due to massive surface precipitation of amorphous UO2-hydroxide phases forming a relatively thick (μm-sized) coating on the carbonate substrate. The interaction of Th with dolomitic marble surface is also intense leading to a formation of an amorphous Th-hydroxide layer of similar thickness but of significantly lower elemental atomic proportion.

Phase I (Year 1) Summary of Research--Establishing the Relationship between Fracture-Related Dolomite and Primary Rock Fabric on the Distribution of Reservoirs in the Michigan Basin

Energy Technology Data Exchange (ETDEWEB)

G. Michael Grammer

2005-11-09

This topical report covers the first 12 months of the subject 3-year grant, evaluating the relationship between fracture-related dolomite and dolomite constrained by primary rock fabric in the 3 most prolific reservoir intervals in the Michigan Basin (Ordovician Trenton-Black River Formations; Silurian Niagara Group; and the Devonian Dundee Formation). Phase I tasks, including Developing a Reservoir Catalog for selected dolomite reservoirs in the Michigan Basin, Characterization of Dolomite Reservoirs in Representative Fields and Technology Transfer have all been initiated and progress is consistent with our original scheduling. The development of a reservoir catalog for the 3 subject formations in the Michigan Basin has been a primary focus of our efforts during Phase I. As part of this effort, we currently have scanned some 13,000 wireline logs, and compiled in excess of 940 key references and 275 reprints that cover reservoir aspects of the 3 intervals in the Michigan Basin. A summary evaluation of the data in these publications is currently ongoing, with the Silurian Niagara Group being handled as a first priority. In addition, full production and reservoir parameter data bases obtained from available data sources have been developed for the 3 intervals in Excel and Microsoft Access data bases. We currently have an excess of 25 million cells of data for wells in the Basin. All Task 2 objectives are on time and on target for Phase I per our original proposal. Our mapping efforts to date, which have focused in large part on the Devonian Dundee Formation, have important implications for both new exploration plays and improved enhanced recovery methods in the Dundee ''play'' in Michigan--i.e. the interpreted fracture-related dolomitization control on the distribution of hydrocarbon reservoirs. In an exploration context, high-resolution structure mapping using quality-controlled well data should provide leads to convergence zones of fault

U-Pb Dating of Calcite to Constrain Basinal Brine Flux Events: An Example from the Upper Midwest USA

Science.gov (United States)

Rasbury, T.; Luczaj, J.

2017-12-01

Calcite forms in a variety of settings and can be the product of surface to deep basinal fluids. As such, this mineral can uniquely record details of the fluids responsible for its formation. The forms of calcium carbonates and their stratigraphic relationships from the thin section to the regional scale give important insights on pulses of fluids. A fundamental question is the age of such fluid pulses. While calcite excludes uranium (U) from its crystal structure, some is incorporated and depending on the U/Pb ratio, this provides an opportunity for radiometric dating. Calcite crystals of various sizes and crystal habits are found in Paleozoic carbonate rocks throughout the region from the western Michigan basin to the upper Mississippi valley. These are typically associated with Mississippi Valley-type (MVT) mineralization, including galena, sphalerite, and iron sulfides, but typically post-date the main MVT event. We have analyzed a variety of these calcites and find multiple generations of calcite, separated by tens of millions of years. The initial Pb isotope ratios are similar to the isotope ratios of nearby galena, strongly suggesting a genetic relationship. Our oldest ages are 200 Ma, and we find ages ranging into the Cenozoic. Based on the Paleozoic-hosted galena Pb-isotope isoscapes from the region, the fluids may have been sourced from both the Michigan and Illinois basins. An important and unanswered question is what would cause significant fluid movement out of the basins substantially after Appalachian orogenesis. Noble gas data from brines in the Michigan Basin have a mantle component and have been suggested to be responsible for recognized elevated temperatures across the basin (Ma et al., 2009). Multiple thermal events during the Paleozoic and Mesozoic eras may have an internal heat source related to reactivation of faults of the Keweenawan Rift system below the Michigan Basin. Perhaps a mantle heat source from below episodically fluxes into the

Fourier Transform Infrared Spectroscopic Determination of Shale ...

African Journals Online (AJOL)

A Classical Least Square (CLS) model was developed from the attenuated spectra of mixtures of five mineral standards chosen to represent the most frequently encountered minerals in shale-type reservoir rocks namely: quartz, illite/smectite (30:70), kaolinite, calcite and dolomite. The CLS model developed was able to ...

Characterization of Shock Effects in Calcite by Raman Spectroscopy: Results of Experiments

Science.gov (United States)

Bell, M. S.

2016-01-01

Carbonates comprise approx. 20% by volume of present day Earth's sedimentary rocks and store most of the terrestrial CO2 inventory. Some of the oldest meta-sedimentary rocks found on Earth contain abundant carbonate from which impact-induced release of CO2 could have played a role in the formation and evolution of the atmosphere. Carbonates are also present in the target materials for approx. 30% of all terrestrial impact structures including large impacts such as Chicxulub which happened to occur at a location with extraordinarily thick platform carbonate 3-6 km deep. The impact release of CO2 from carbonates can cause global warming as a result of the well-known greenhouse effect and have subsequent effects on climate and biota. Therefore, the shock behavior of calcite is important in understanding the Cretaceous-Paleogene event and other impacts with carbonate-bearing sediments in their target(s) such as Mars and some asteroids. A comprehensive survey utilizing a variety of techniques to characterize the effects manifest in Calcite (Iceland Spar) experimentally shocked to 60.8 GPa has been completed. Results of analysis by Raman Spectroscopy are reported here.

Biomineralization processes of calcite induced by bacteria isolated from marine sediments.

Science.gov (United States)

Wei, Shiping; Cui, Hongpeng; Jiang, Zhenglong; Liu, Hao; He, Hao; Fang, Nianqiao

2015-06-01

Biomineralization is a known natural phenomenon associated with a wide range of bacterial species. Bacterial-induced calcium carbonate precipitation by marine isolates was investigated in this study. Three genera of ureolytic bacteria, Sporosarcina sp., Bacillus sp. and Brevundimonas sp. were observed to precipitate calcium carbonate minerals. Of these species, Sporosarcina sp. dominated the cultured isolates. B. lentus CP28 generated higher urease activity and facilitated more efficient precipitation of calcium carbonate at 3.24 ± 0.25 × 10(-4) mg/cell. X-ray diffraction indicated that the dominant calcium carbonate phase was calcite. Scanning electron microscopy showed that morphologies of the minerals were dominated by cubic, rhombic and polygonal plate-like crystals. The dynamic process of microbial calcium carbonate precipitation revealed that B. lentus CP28 precipitated calcite crystals through the enzymatic hydrolysis of urea, and that when ammonium ion concentrations reached 746 mM and the pH reached 9.6, that favored calcite precipitation at a higher level of 96 mg/L. The results of this research provide evidence that a variety of marine bacteria can induce calcium carbonate precipitation, and may influence the marine carbonate cycle in natural environments.

Dedolomitization Potential of Fluids from Gypsum-to-Anhydrite Conversion: Mass Balance Constraints from the Late Permian Zechstein-2-Carbonates in NW Germany

Directory of Open Access Journals (Sweden)

M. Hallenberger

2018-01-01

Full Text Available The Zechstein-2-Carbonates represent one of the most prolific hydrocarbon systems of Central Europe. Carbonate reservoir quality is primarily controlled by mineralogy, with dolomite representing moderate-to-good porosities and calcite commonly representing low porosities. Current models suggest that this calcite is the result of a basin-wide phase of dedolomitization. The calcium (Ca source for the dedolomites is thought to be derived from the fluids liberated during gypsum-to-anhydrite conversion. We present an easy-to-use and generally applicable template to estimate the dedolomitization potential of these fluids. Depending on reaction stoichiometry, salinity, and temperature, we estimate that between 2.8⁎10−3 m3 and 6.2⁎10−3 m3 of calcite may replace dolomite for each m3 of anhydrite created. Within the constraints dictated by the environment of the late Permian Zechstein basin, we estimate that about 5⁎10−3 m3 of dedolomite is created for each m3 of anhydrite. Mass balance constraints indicate that fluids derived from gypsum-to-anhydrite conversion account for less than 1% of the observed dedolomite in most of the studied industry wells from northern Germany.

Formation and mosaicity of coccolith segment calcite of the marine algae Emiliania huxleyi.

Science.gov (United States)

Yin, Xiaofei; Ziegler, Andreas; Kelm, Klemens; Hoffmann, Ramona; Watermeyer, Philipp; Alexa, Patrick; Villinger, Clarissa; Rupp, Ulrich; Schlüter, Lothar; Reusch, Thorsten B H; Griesshaber, Erika; Walther, Paul; Schmahl, Wolfgang W

2018-02-01

Coccolithophores belong to the most abundant calcium carbonate mineralizing organisms. Coccolithophore biomineralization is a complex and highly regulated process, resulting in a product that strongly differs in its intricate morphology from the abiogenically produced mineral equivalent. Moreover, unlike extracellularly formed biological carbonate hard tissues, coccolith calcite is neither a hybrid composite, nor is it distinguished by a hierarchical microstructure. This is remarkable as the key to optimizing crystalline biomaterials for mechanical strength and toughness lies in the composite nature of the biological hard tissue and the utilization of specific microstructures. To obtain insight into the pathway of biomineralization of Emiliania huxleyi coccoliths, we examine intracrystalline nanostructural features of the coccolith calcite in combination with cell ultrastructural observations related to the formation of the calcite in the coccolith vesicle within the cell. With TEM diffraction and annular dark-field imaging, we prove the presence of planar imperfections in the calcite crystals such as planar mosaic block boundaries. As only minor misorientations occur, we attribute them to dislocation networks creating small-angle boundaries. Intracrystalline occluded biopolymers are not observed. Hence, in E. huxleyi calcite mosaicity is not caused by occluded biopolymers, as it is the case in extracellularly formed hard tissues of marine invertebrates, but by planar defects and dislocations which are typical for crystals formed by classical ion-by-ion growth mechanisms. Using cryo-preparation techniques for SEM and TEM, we found that the membrane of the coccolith vesicle and the outer membrane of the nuclear envelope are in tight proximity, with a well-controlled constant gap of ~4 nm between them. We describe this conspicuous connection as a not yet described interorganelle junction, the "nuclear envelope junction". The narrow gap of this junction likely

Cyclic carbonation calcination studies of limestone and dolomite for CO{sub 2} separation from combustion flue gases - article no. 011801

Energy Technology Data Exchange (ETDEWEB)

Senthoorselvan, S.; Gleis, S.; Hartmut, S.; Yrjas, P.; Hupa, M. [TUM, Garching (Germany)

2009-01-15

Naturally occurring limestone and dolomite samples, originating from different geographical locations, were tested as potential sorbents for carbonation/calcination based CO{sub 2} capture from combustion flue gases. Samples have been studied in a thermogravimetric analyzer under simulated flue gas conditions at three calcination temperatures, viz., 750{sup o}C, 875{sup o}C, and 930{sup o}C for four carbonation calcination reaction (CCR) cycles. The dolomite sample exhibited the highest rate of carbonation than the tested limestones. At the third cycle, its CO{sub 2} capture capacity per kilogram of the sample was nearly equal to that of Gotland, the highest reacting limestone tested. At the fourth cycle it surpassed Gotland, despite the fact that the CaCO{sub 3} content of the Sibbo dolomite was only 2/3 of that of the Gotland. Decay coefficients were calculated by a curve fitting exercise and its value is lowest for the Sibbo dolomite. That means, most probably its capture capacity per kilogram of the sample would remain higher well beyond the fourth cycle. There was a strong correlation between the calcination temperature, the specific surface area of the calcined samples, and the degree of carbonation. It was observed that the higher the calcination temperature, the lower the sorbent reactivity. For a given limestone/dolomite sample, sorbents CO{sub 2} capture capacity depended on the number of CCR cycles and the calcination temperature. According to the equilibrium thermodynamics, the CO{sub 2} partial pressure in the calciner should be lowered to lower the calcination temperature. This can be achieved by additional steam supply into the calciner. Steam could then be condensed in an external condenser to single out the CO{sub 2} stream from the exit gas mixture of the calciner. A calciner design based on this concept is illustrated.

Calcite growth-rate inhibition by fulvic acids isolated from Big Soda Lake, Nevada, USA, The Suwannee River, Georgia, USA and by polycarboxylic acids

Science.gov (United States)

Reddy, Michael M.; Leenheer, Jerry

2011-01-01

Calcite crystallization rates are characterized using a constant solution composition at 25°C, pH=8.5, and calcite supersaturation (Ω) of 4.5 in the absence and presence of fulvic acids isolated from Big Soda Lake, Nevada (BSLFA), and a fulvic acid from the Suwannee River, Georgia (SRFA). Rates are also measured in the presence and absence of low-molar mass, aliphatic-alicyclic polycarboxylic acids (PCA). BSLFA inhibits calcite crystal-growth rates with increasing BSLFA concentration, suggesting that BSLFA adsorbs at growth sites on the calcite crystal surface. Calcite growth morphology in the presence of BSLFA differed from growth in its absence, supporting an adsorption mechanism of calcite-growth inhibition by BSLFA. Calcite growth-rate inhibition by BSLFA is consistent with a model indicating that polycarboxylic acid molecules present in BSLFA adsorb at growth sites on the calcite crystal surface. In contrast to published results for an unfractionated SRFA, there is dramatic calcite growth inhibition (at a concentration of 1 mg/L) by a SRFA fraction eluted by pH 5 solution from XAD-8 resin, indicating that calcite growth-rate inhibition is related to specific SRFA component fractions. A cyclic PCA, 1, 2, 3, 4, 5, 6-cyclohexane hexacarboxylic acid (CHXHCA) is a strong calcite growth-rate inhibitor at concentrations less than 0.1 mg/L. Two other cyclic PCAs, 1, 1 cyclopentanedicarboxylic acid (CPDCA) and 1, 1 cyclobutanedicarboxylic acid (CBDCA) with the carboxylic acid groups attached to the same ring carbon atom, have no effect on calcite growth rates up to concentrations of 10 mg/L. Organic matter ad-sorbed from the air onto the seed crystals has no effect on the measured calcite crystal-growth rates.

Fluid-chemical evidence for one billion years of fluid flow through Mesoproterozoic deep-water carbonate mounds (Nanisivik zinc district, Nunavut)

Science.gov (United States)

Hahn, K. E.; Turner, E. C.; Kontak, D. J.; Fayek, M.

2018-02-01

Ancient carbonate rocks commonly contain numerous post-depositional phases (carbonate minerals; quartz) recording successive diagenetic events that can be deciphered and tied to known or inferred geological events using a multi-pronged in situ analytical protocol. The framework voids of large, deep-water microbial carbonate seep-mounds in Arctic Canada (Mesoproterozoic Ikpiarjuk Formation) contain multiple generations of synsedimentary and late cement. An in situ analytical study of the post-seafloor cements used optical and cathodoluminescence petrography, SEM-EDS analysis, fluid inclusion (FI) microthermometry and evaporate mound analysis, LA-ICP-MS analysis, and SIMS δ18O to decipher the mounds' long-term diagenetic history. The six void-filling late cements include, in paragenetic order: inclusion-rich euhedral dolomite (ED), finely crystalline clear dolomite (FCD), hematite-bearing dolomite (HD), coarsely crystalline clear dolomite (CCD), quartz (Q), replacive calcite (RC) and late calcite (LC). Based on the combined analytical results, the following fluid-flow history is defined: (1) ED precipitation by autocementation during shallow burial (fluid 1; Mesoproterozoic); (2) progressive mixing of Ca-rich hydrothermal fluid with the connate fluid, resulting in precipitation of FCD followed by HD (fluid 2; also Mesoproterozoic); (3) precipitation of hydrothermal dolomite (CCD) from high-Ca and K-rich fluids (fluid 3; possibly Mesoproterozoic, but timing unclear); (4) hydrothermal Q precipitation (fluid 4; timing unclear), and (5) RC and LC precipitation from a meteoric-derived water (fluid 5) in or since the Mesozoic. Fluids associated with FCD, HD, and CCD may have been mobilised during deposition of the upper Bylot Supergroup; this time interval was the most tectonically active episode in the region's Mesoproterozoic to Recent history. The entire history of intermittent fluid migration and cement precipitation recorded in seemingly unimportant void

The Labrador Sea during the Last Glacial Maximum: Calcite dissolution or low biogenic carbonate fluxes?

Science.gov (United States)

Marshall, Nicole; de Vernal, Anne; Mucci, Alfonso; Filippova, Alexandra; Kienast, Markus

2017-04-01

Low concentrations of biogenic carbonate characterize the sediments deposited in the Labrador Sea during the last glaciation. This may reflect poor calcite preservation and/or low biogenic carbonate productivity and fluxes. Regional bottom water ventilation was reduced during the Last Glacial Maximum (LGM), so the calcite lysocline might have been shallower than at present in the deep Labrador Sea making dissolution of calcite shells in the deep Labrador Sea possible. To address the issue, a multi-proxy approach based on micropaleontological counts (coccoliths, foraminifers, palynomorphs) and biogeochemical analyses (alkenones) was applied in the investigation of core HU2008-029-004-PC recovered in the northwestern Labrador Sea. Calcite dissolution indices based on the relative abundance benthic foraminifera shells to their organic linings as well as on fragmentation of planktonic foraminifera shells were used to evaluate changes in calcite dissolution/ preservation since the LGM. In addition, the ratio of the concentrations of coccoliths, specifically of the alkenone-producer Emiliania huxleyi, and alkenones (Emiliania huxleyi: alkenones) was explored as a potential new proxy of calcite dissolution. A sharp increase in coccoliths, foraminifers and organic linings from nearly none to substantial concentrations at 12 ka, reflect a jump to significantly greater biogenic fluxes at the glacial-interglacial transition. Furthermore, conventional dissolution indices (shells/linings of benthic foraminifera and fragmentation of planktic foraminifers) reveal that dissolution is not likely responsible for the lower glacial abundances of coccoliths and foraminifers. Only the low Emiliania huxleyi: alkenones ratios in glacial sediments could be interpreted as evidence of increased dissolution during the LGM. Given the evidence of allochthonous alkenone input into the glacial Labrador Sea, the latter observations must be treated with caution. Overall, the records indicate that

Morphology and formation mechanism in precipitation of calcite induced by Curvibacter lanceolatus strain HJ-1

Science.gov (United States)

Zhang, Chonghong; Li, Fuchun; Lv, Jiejie

2017-11-01

Precipitation of calcium carbobate induced by microbial activities is common occurrence in controlled solution, but the formation mechanism and morphology in precipitation of calcite in solution systems is unclear, and the role of microbes is disputed. Here, culture experiment was performed for 50 days using the Curvibacter lanceolatus strain HJ-1 in a M2 culture medium, and the phase composition and morphology of the precipitates were characterized by the X-ray diffraction (XRD), Fourier transform infrared (FT-IR), and scanning electron microscopy (SEM) techniques. We show that the precipitation processes in our experiment lead to unusual morphologies of crystals corresponding to different growth stages, and the morphologies of the precipitated crystal aggregates ranging from the main rod-, cross-, star-, cauliflower-like morphologies to spherulitic structure. The complex and unusual morphologies of the precipitated calcite by strain HJ-1 may provide a reference point for better understanding the biomineralization mechanism of calcite, moreover, morphological transition of minerals revealed that the multi-ply crystals-aggregation mechanism for calcite growth in crystallisation media.

Thermoluminescence and cathodoluminescence studies of calcite and MgO: surface defects and heat treatment

International Nuclear Information System (INIS)

Goeksu, H.Y.; Brown, L.M.

1988-01-01

Some of the problems which preclude accurate thermoluminescence (TL) dating of geologically formed calcite stem from different sample pre-treatment procedures, such as grinding, drilling or pre-heating. It has long been known that grinding can introduce spurious TL in calcite, but there have been wide differences of opinion as to the magnitude of the influence and its importance. Therefore, various grinding and acid-washing procedures have been suggested to avoid spurious thermoluminescence. Various models have been developed to explain the mechanism. We have studied the changes in thermoluminescence (TL) and cathodoluminescence (CL) properties as well as in the spectral composition of the glow from calcite and MgO due to surface defects and heat treatment. It is found that both laboratory heat treatment and surface indents give rise to changes in TL efficiency. (author)

Neutron-activation determination of the rare earths in natural calcites using a semiconductor detector

International Nuclear Information System (INIS)

Vaganov, N.A.; Bulnaev, A.I.; Mejer, V.A.; Ponomarev, V.S.

1976-01-01

The application of germanium semiconducting detector is described. The detector has an energy resolution about 1 KeV and makes it possible to determine the content of Ce, Nd, Eu, Gd, Tb, and Yb in natural calcites with high sensitivity. The region of soft γ-radiation of activated calcites is more favourable for measurements to be performed than the region of hard γ-rays. Semiconducting detectors of radiation type are relatively cheap; they can be stored at room temperature. The limit of determining rare earth elements in calcites is (g): Eu-1.5.10 -9 ; Tb-4.0.10 -9 ; Yb-7.0.10 -9 ; Ce-1.0.10 -7 ; Nd-5.0.10 -7 ; Gd-1.0.10 -6 . A relative error of concentration determination is 10-20%

The effect of heat treatment on the thermoluminescence of naturally-occurring calcites and their use as a gamma-ray dosimeter

International Nuclear Information System (INIS)

Engin, Birol; Gueven, Olgun

2000-01-01

The feasibility of using naturally-occurring calcite for gamma-ray dosimetry was investigated. Anneal treatment above 350 deg. C increased the sensitivity of all radiation-induced TL peaks except the glow peaks above 300 deg. C. On the other hand, annealing in air, at a temperature of 700 deg. C caused a collapse in the TL sensitivity. The increase in TL efficiency was found to depend on the annealing temperature and time. Heating at 600 deg. C for 5 h and quenching in ambient air are the optimum conditions for TL sensitivity enhancement in the calcite materials investigated. These results are explained using the energy scheme of the pre-dose model of and in terms of the impurity rearrangements in the crystal lattice induced by heating. It was found that the values of the kinetic parameters E, s and b for TL glow peaks remained unchanged for annealed samples. The TL dose-response curves for stable dosimetric peaks of annealed and unannealed calcite samples could be fitted to the same linear mathematical function. This implies that the annealing process probably does not change the nature of the trapping centers except the low temperature TL peaks at 125 and 160 deg. C of flowstone. The TL dosimetric parameters of calcite samples annealed, including glow curves, fading characteristics, dose-responses, dose-rate responses and energy responses, have also been studied in detail. The response to gamma-rays of annealed calcite samples was found to be linear from 0.05 to 10 4 Gy. The lower limit of observable doses for each calcite sample was about 0.05 Gy. This offers the possibility of applying the investigated materials for gamma-ray dosimetry within this useful range. These dosimeters can be used in various applications, such as, in industries related to chemical technology (polymerization), food processing and in determining the dose received by the patient during medical examination and treatment

Molecular modeling studies of interactions between sodium polyacrylate polymer and calcite surface

Energy Technology Data Exchange (ETDEWEB)

Ylikantola, A. [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); Linnanto, J., E-mail: juha.m.linnanto@gmail.com [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); University of Tartu, Institute of Physics, Riia 142, EE-51014 Tartu (Estonia); Knuutinen, J.; Oravilahti, A. [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); Toivakka, M. [Åbo Akademi University, Laboratory of Paper Coating and Converting and Center for Functional Materials, FI-20500 Turku/Åbo (Finland)

2013-07-01

The interactions between calcite pigment and sodium polyacrylate dispersing agent, widely used in papermaking as paper coating components, were investigated using classical force field and quantum chemical approaches. The objective was to understand interactions between the calcite surface and sodium polyacrylate polymer at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the sodium polyacrylate polymer structure. The effect of water molecules (moisture) on the interactions was also examined. Calculations showed that molecular weight, branching and the orientation of sodium polyacrylate polymers influence the interactions between the calcite surface and the polymer. The force field applied, and also water molecules, were found to have an impact on all systems studied. Ab initio Hartree–Fock calculations indicated that there are two types of coordination between sodium atoms and carboxylate groups of the sodium polyacrylate polymer, inter- and intra-carboxylate group coordination. In addition, ab initio Hartree–Fock calculations of the structure of the sodium polyacrylate polymer produced important information regarding interactions between the polymers and carboxylated styrene-butadiene latex particles.

High School Forum: "Invitations to Enquiry": The Calcite/Acid Reaction.

Science.gov (United States)

Herron, J. Dudley, Ed.; Driscoll, D. R.

1979-01-01

Describes a high school chemistry experiment which involves the reaction between calcite and hydrochloric and sulfuric acids. This reaction can be carried out as a projected demonstration and on an individual basis. (HM)

Utilization of calcite produced in Turkey for paper coating

Directory of Open Access Journals (Sweden)

Hüdaverdi Eroğlu

2002-03-01

Full Text Available Calcium carbonate is one of the coating pigments widely used in paper industry. Especially, in recent years calcium carbonate filler has gained high importance in alkaline pulping. In Turkey industry actually imports calcium carbonate; whereas, there are rich calcite reservoirs in the country. In this study two different types of domestic ground (GCC calcite samples were used. Physical and chemical properties of calcite samples were tested firstly. CaCO3 percentages of both samples were 97.3 % and 97.6 % (min. 95 % CaCO3. MgCO3 and Fe2O3 percentages were within the desired limits. Brightness values were 95.5 % and 94.5 % and yellowness 1.1 % and 1.5 % elrepho. These values also were within the requested limits. Under 2 microns particle size and over 10 microns particle size fractions were 95 % and 89 % (min. 80 and 1 % and 2 % (max. 2 respectively. Dry matter rates were between 40 %-65 %, for the pilot plant-coating machine. During the preparation of coating color calcium carbonate has been used together with kaolin. The ratios of calcium carbonate to kaolin were 30/70, 40/60, 50/50, 60/40, 70/30, 100/0. In coating color preparation latex was used as a binder because of its wide applications. Latex percentages were 11, 12, and 13 %. Coated papers were glossed and physically tested. As a result, both calcium carbonate samples were found suitable for using in coating color preparation. By the utilization of domestic calcium carbonate in coated paper production, there will be foreign currencies saving.

Geology and permian paleomagnetism of the Val-di-Non area W. Dolomites, N. Italy

NARCIS (Netherlands)

van Hilten, D.

1960-01-01

During the summers of 1957 till 1959 geological investigations were carried out in the western part of the Dolomites (southern Alps), where these are separated from the central Alps by the Judicaria fault. A long time before the principal displacements occurred along this fault - late oligocene -

Geology and permian paleomagnetism of the Val-di-Non area W. Dolomites, N. Italy

NARCIS (Netherlands)

Hilten, D. van

1960-01-01

During the summers of 1957 till 1959 geological investigations were carried out in the western part of the Dolomites (southern Alps), where these are separated from the central Alps by the Judicaria fault. A long time before the principal displacements occurred along this fault - late oligocene

Microstructural Damage During High-Strain Torsion Experiments on Calcite-Anhydrite Aggregates

Science.gov (United States)

Cross, A. J.; Skemer, P. A.

2016-12-01

Ductile shear zones play a critical role in localising deformation in the Earth's crust and mantle. Severe grain size reduction - a ubiquitous feature of natural mylonites - is commonly thought to cause strain weakening via a transition to grain size sensitive deformation mechanisms. Although grain size reduction is modulated by grain growth in single-phase aggregates, grain boundary pinning in well-mixed poly-phase composites can inhibit grain growth, leading to microstructural `damage' which is likely a critical element of strain localization in the lithosphere. While dynamic recrystallization has been widely explored in rock mechanics and materials science, the mechanisms behind phase-mixing remain poorly understood. In this contribution we present results from high-strain, deformation experiments on calcite-anhydrite composites. Experiments were conducted in torsion at T = 500-700°C and P 1.5 GPa, using the new Large Volume Torsion (LVT) solid-medium apparatus, to shear strains of 0.5-30. As shear strain increases, progressive thinning and necking of initially large (≤ 1 mm) calcite domains is observed, resulting in an increase in the proportion of interphase boundaries. Grain-size is negatively correlated with the fraction of interphase boundaries, such that calcite grains in well-mixed regions are significantly smaller than those in single-phase domains. Crucially, progressive deformation leads to a reduction in grain-size beyond the lower limit established by the grain size piezometer for mono-phase calcite, implying microstructural damage. These data therefore demonstrate continued microstructural evolution in two-phase composites that is not possible in single-phase aggregates. These observations mark a new `geometric' mechanism for phase mixing, complementing previous models for phase mixing involving chemical reactions, material diffusion, and/or grain boundary sliding.

Radiation-induced paramagnetic species in natural calcite speleothems

International Nuclear Information System (INIS)

Rossi, A.M.; Poupeau, G.

1989-01-01

The ESR natural spectrum of humic-free speleothem calcite single crytals in the region of g = 2.0000 is a composite of lines from 4 radiogenic species, in addition to Mn ++ lines. Laboratory irradiation causes appearrance of three more species. Use of isotropic F species (g = 2.0003) for dating is possible if specific cautions are followed. (author) [pt

Calcite as a bone substitute. Comparison with hydroxyapatite and tricalcium phosphate with regard to the osteoblastic activity

Energy Technology Data Exchange (ETDEWEB)

Monchau, F., E-mail: Francine.monchau@univ-artois.fr [Laboratoire Genie Civil et geo-Environnement (EA 4515, Universite Lille Nord de France), Equipe Biomateriaux Artois (Universite d' Artois), IUT/GMP, 1230, rue de l' Universite, BP 819, 62408 Bethune cedex (France); Hivart, Ph.; Genestie, B. [Laboratoire Genie Civil et geo-Environnement (EA 4515, Universite Lille Nord de France), Equipe Biomateriaux Artois (Universite d' Artois), IUT/GMP, 1230, rue de l' Universite, BP 819, 62408 Bethune cedex (France); Chai, F. [Laboratoire Medicaments et Biomateriaux a Liberation Controlee (INSERM U 1008, Universite Lille Nord de France), Groupe de Recherche sur les Biomateriaux (Universite Lille-2), Faculte de Medecine, 1, place de Verdun, 59045 Lille cedex (France); and others

2013-01-01

Close to the bone mineral phase, the calcic bioceramics, such as hydroxyapatite (HA) and {beta}-tricalcium phosphate ({beta}-TCP), are commonly used as substitutes or filling materials in bone surgery. Besides, calcium carbonate (CaCO{sub 3}) is also used for their excellent biocompatibility and bioactivity. However, the problem with the animal-origin aragonite demands the new technique to synthesize pure calcite capable of forming 3D bone implant. This study aims to manufacture and evaluate a highly-pure synthetic crystalline calcite with good cytocompatibility regarding to the osteoblasts, comparing to that of HA and {beta}-TCP. After the manufacture of macroporous bioceramic scaffolds with the identical internal architecture, their cytocompatibility is studied through MC3T3-E1 osteoblasts with the tests of cell viability, proliferation, vitality, etc. The results confirmed that the studied process is able to form a macroporous material with a controlled internal architecture, and this synthesized calcite is non-cytotoxic and facilitate the cell proliferation. Indeed requiring further improvement, the studied calcite is definitely an interesting alternative not only to coralline aragonite but also to calcium phosphate ceramics, particularly in bone sites with the large bone remodelling. Highlights: Black-Right-Pointing-Pointer Macroporous calcite manufacturing with controlled architecture as bone substitute Black-Right-Pointing-Pointer Cytotoxicity: adaptation of the colony-forming method with the target cells: MC3T3-E1 osteoblasts Black-Right-Pointing-Pointer Study of osteoblast proliferation and activity on calcite, HA and TCP.

Olivine, dolomite and ceramic filters in one vessel to produce clean gas from biomass.

Science.gov (United States)

Rapagnà, Sergio; Gallucci, Katia; Foscolo, Pier Ugo

2018-01-01

Heavy organic compounds produced during almond shells gasification in a steam and/or air atmosphere, usually called tar, are drastically reduced in the product gas by using simultaneously in one vessel a ceramic filter placed in the freeboard and a mixture of olivine and dolomite particles in the fluidized bed of the gasifier. The content of tar in the product gas during a reference gasification test with air, in presence of fresh olivine particles only, was 8600mg/Nm 3 of dry gas. By gasifying biomass with steam at the same temperature level of 820°C in a bed of olivine and dolomite (20% by weight), and in the presence of a catalytic ceramic filter inserted in the freeboard of the fluidized bed gasifier, the level of tar was brought down to 57mg/Nm 3 of dry producct gas, with a decrease of more than two orders of magnitude. Copyright © 2017 Elsevier Ltd. All rights reserved.

Fluid inclusion studies of calcite veins from Yucca Mountain, Nevada, Tuffs: Environment of formation

International Nuclear Information System (INIS)

Roedder, E.; Whelan, J.F.; Vaniman, D.T.

1994-01-01

Calcite vein and vug fillings at fourth depths (130-314m), all above the present water table in USW G-1 bore hole at Yucca Mountain, Nevada, contain primary fluid inclusions with variable vapor/liquid ratios: most of these inclusions are either full of liquid or full of vapor. The liquid-filled inclusions show that most of the host calcite crystallized from fluids at 2 vapor phase at open-quotes 100 degrees Cclose quotes. Our new studies reveal the additional presence of major methane in the vapor-filled inclusion, indicating even lower temperatures of trapping, perhaps at near-surface temperatures. They also show that the host calcite crystals grew from a flowing film of water on the walls of fractures open to the atmosphere, the vapor-filled inclusions representing bubbles that exsolved from this film onto the crystal surface

Fluid inclusion studies of calcite veins from Yucca Mountain, Nevada, Tuffs: Environment of formation

International Nuclear Information System (INIS)

Roedder, E.; Whelan, J.F.; Vaniman, D.T.

1994-01-01

Calcite vein and vug fillings at four depths (130-314m), all above the present water table in USW G-1 bore hole at Yucca Mountain, Nevada, contain primary fluid inclusions with variable vapor/liquid raitos: Most of these inclusions are either full of liquid or full of vapor. The liquid-filled inclusions show that most of the host calcite crystallized from fluids at 2 vapor phase at ''<100 degrees C''. Our new studies reveal the additional presence of major methane in the vapor-filled inclusion, indicating even lower temperatures of trapping, perhaps at near-surface temperatures. They also show that the host calcite crystals grew from a flowing film of water on the walls of fractures open to the atmosphere, the vapor-filled inclusions representing bubbles that exsolved from this film onto the crystal surface

THE EFFECT OF FISSURES IN DOLOMITE ROCK MASS ON BLASTING PROJECTS

Directory of Open Access Journals (Sweden)

Branko Božić

1989-12-01

Full Text Available Rock fractures in the form of fissures are one of more important geological features of a tectonic system. They have an effect on mechanical behaviour of rook masses exposed to the actions of surface forces. For exploitation in dolomite quarries carried out by blasting of deep shot holes it is important to know the system of fissures within a rock mass for the rock brakes along already weakened planes (the paper is published in Croatian.

Diagenesis of silica-rich mounded chalk, the Coniacian Arnager Limestone, Denmark

DEFF Research Database (Denmark)

Buus Madsen, Heine; Stemmerik, Lars; Surlyk, Finn

2010-01-01

The Coniacian Arnager Limestone Formation is exposed on the Danish island of Bornholm in the Baltic Sea. It is composed of mound-bedded siliceous chalk, and X-ray diffraction and scanning electron microscopy indicate a content of 30-70% insoluble minerals, including authigenic opal-CT, quartz......, clinoptilolite, feldspars, calcite, dolomite, and barite. Opal-CT and clinoptilolite are the most common and constitute 16-53% and 2-9%, respectively. The content of insoluble minerals varies laterally bothwithinthemounds and inplanar beds, and the opal-CT content varies by up to 10% vertically. Themounds...... precipitation of opal-CT. The opal-CT formed at temperatures around 17°C, the precipitation lowered the silica activity and the Si/Al ratio of the pore water, resulting in precipitation of clinoptilolite, feldspar and smectite. Calcite formed synchronouslywith the latest clinoptilolite.Minoramounts of quartz...

Three-dimensional hydration layer mapping on the (10.4) surface of calcite using amplitude modulation atomic force microscopy.

Science.gov (United States)

Marutschke, Christoph; Walters, Deron; Walters, Deron; Hermes, Ilka; Bechstein, Ralf; Kühnle, Angelika

2014-08-22

Calcite, the most stable modification of calcium carbonate, is a major mineral in nature. It is, therefore, highly relevant in a broad range of fields such as biomineralization, sea water desalination and oil production. Knowledge of the surface structure and reactivity of the most stable cleavage plane, calcite (10.4), is pivotal for understanding the role of calcite in these diverse areas. Given the fact that most biological processes and technical applications take place in an aqueous environment, perhaps the most basic - yet decisive - question addresses the interaction of water molecules with the calcite (10.4) surface. In this work, amplitude modulation atomic force microscopy is used for three-dimensional (3D) mapping of the surface structure and the hydration layers above the surface. An easy-to-use scanning protocol is implemented for collecting reliable 3D data. We carefully discuss a comprehensible criterion for identifying the solid-liquid interface within our data. In our data three hydration layers form a characteristic pattern that is commensurate with the underlying calcite surface.

Three-dimensional hydration layer mapping on the (10.4) surface of calcite using amplitude modulation atomic force microscopy

International Nuclear Information System (INIS)

Marutschke, Christoph; Hermes, Ilka; Bechstein, Ralf; Kühnle, Angelika; Walters, Deron; Cleveland, Jason

2014-01-01

Calcite, the most stable modification of calcium carbonate, is a major mineral in nature. It is, therefore, highly relevant in a broad range of fields such as biomineralization, sea water desalination and oil production. Knowledge of the surface structure and reactivity of the most stable cleavage plane, calcite (10.4), is pivotal for understanding the role of calcite in these diverse areas. Given the fact that most biological processes and technical applications take place in an aqueous environment, perhaps the most basic—yet decisive—question addresses the interaction of water molecules with the calcite (10.4) surface. In this work, amplitude modulation atomic force microscopy is used for three-dimensional (3D) mapping of the surface structure and the hydration layers above the surface. An easy-to-use scanning protocol is implemented for collecting reliable 3D data. We carefully discuss a comprehensible criterion for identifying the solid–liquid interface within our data. In our data three hydration layers form a characteristic pattern that is commensurate with the underlying calcite surface. (paper)

Thickness and structure of the water film deposited from vapour on calcite surfaces

DEFF Research Database (Denmark)

Bohr, Jakob; Wogelius, Roy A.; Morris, Peter M.

2010-01-01

Synchrotron X-ray reflectivity (SXR) was used to measure the thickness of the water film that adsorbs on a {10¯14} cleavage surface of calcite (CaCO3) in a sample chamber where relative humidity could be controlled within the range from......Synchrotron X-ray reflectivity (SXR) was used to measure the thickness of the water film that adsorbs on a {10¯14} cleavage surface of calcite (CaCO3) in a sample chamber where relative humidity could be controlled within the range from...

Inhibiting Effect of Additives on Pressure Solution of Calcite

Science.gov (United States)

Traskine, V.; Skvortsova, Z.; Badun, G.; Chernysheva, M.; Simonov, Ya.; Gazizullin, I.

2018-05-01

The task of protection of cultural heritage requires a better understanding of combined effects of mechanical and chemical factors involved in environmental deterioration of monuments. The present paper deals with extending some known physicochemical methods proposed for inhibiting the decay of unstressed materials to their study during water-assisted deformation. The tests have been carried out on natural limestone samples and calcite powders in CaCO3 saturated aqueous solutions under static loads causing measurable pressure solution creep. In the solutions containing 1-hydroxyethylidene-1,1-diphosphonic acid, nitrilotriacetic acid, or ethylenediaminetetraacetic acid, the creep rate decreases considerably with increasing concentration of additives. The extent of creep deceleration has been found to be proportional to the independently estimated calcite surface area occupied by adsorbed species. This fact enables us to discriminate the adsorption-induced effect from other variables controlling the pressure solution rate and may be used in screening of compounds able to minimize the environmental impact on marble and limestone objects undergoing mechanical stresses.

Interaction of europium and nickel with calcite studied by Rutherford Backscattering Spectrometry and Time-Resolved Laser Fluorescence Spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Sabau, A. [Agence Nationale pour la gestion des Déchets RAdioactifs, 1-7 rue J. Monnet, Parc de la Croix Blanche, 92298 Châtenay-Malabry Cedex (France); Université de Nice Sophia Antipolis, Ecosystèmes Côtiers Marins et Réponses aux Stress (ECOMERS), 28 avenue Valrose, 06108 Nice Cedex 2 (France); Pipon, Y., E-mail: pipon@ipnl.in2p3.fr [Institut de Physique Nucléaire de Lyon (IPNL), Université Lyon 1, CNRS/IN2P3, 4 rue Enrico Fermi, 69 622 Villeurbanne Cedex (France); Institut Universitaire de Technologie (IUT) Lyon-1, Université Claude Bernard Lyon 1, 69 622 Villeurbanne Cedex (France); Toulhoat, N. [Institut de Physique Nucléaire de Lyon (IPNL), Université Lyon 1, CNRS/IN2P3, 4 rue Enrico Fermi, 69 622 Villeurbanne Cedex (France); CEA/DEN, Saclay, 91191 Gif sur Yvette (France); Lomenech, C. [Université de Nice Sophia Antipolis, Ecosystèmes Côtiers Marins et Réponses aux Stress (ECOMERS), 28 avenue Valrose, 06108 Nice Cedex 2 (France); Jordan, N. [Helmholtz Zentrum Dresden Rossendorf (HZDR), Institute of Resource Ecology (IRE) (Germany); Moncoffre, N. [Institut de Physique Nucléaire de Lyon (IPNL), Université Lyon 1, CNRS/IN2P3, 4 rue Enrico Fermi, 69 622 Villeurbanne Cedex (France); Barkleit, A. [Helmholtz Zentrum Dresden Rossendorf (HZDR), Institute of Resource Ecology (IRE) (Germany); and others

2014-08-01

This study aims at elucidating the mechanisms regulating the interaction of Eu and Ni with calcite (CaCO{sub 3}). Calcite powders or single crystals (some mm sized) were put into contact with Eu or Ni solutions at concentrations ranging from 10{sup −3} to 10{sup −5} mol L{sup −1} for Eu and 10{sup −3} mol L{sup −1} for Ni. The sorption durations ranged from 1 week to 1 month. Rutherford Backscattering Spectrometry (RBS) well adapted to discriminate incorporation processes such as: (i) adsorption or co precipitation at the mineral surfaces or, (ii) incorporation into the mineral structure (through diffusion for instance), has been carried out. Moreover, using the fluorescence properties of europium, the results have been compared to those obtained by Time-Resolved Laser Fluorescence Spectroscopy (TRLFS) on calcite powders. For the single crystals, complementary SEM observations of the mineral surfaces at low voltage were also performed. Results showed that Ni accumulates at the calcite surface whereas Eu is also incorporated at a greater depth. Eu seems therefore to be incorporated into two different states in calcite: (i) heterogeneous surface accumulation and (ii) incorporation at depth greater than 160 nm after 1 month of sorption. Ni was found to accumulate at the surface of calcite without incorporation.

Relative Shock Effects in Mixed Powders of Calcite, Gypsum, and Quartz: A Calibration Scheme from Shock Experiments

Science.gov (United States)

Bell, Mary S.

2009-01-01

The shock behavior of calcite and gypsum is important in understanding the Cretaceous/Tertiary event and other terrestrial impacts that contain evaporite sediments in their targets. Most interest focuses on issues of devolatilization to quantify the production of CO2 or SO2 to better understand their role in generating a temporary atmosphere and its effects on climate and biota [e.g., papers in 1,2,3,4]. Devolatilization of carbonate is also important because the dispersion and fragmentation of ejecta is strongly controlled by the expansion of large volumes of gas during the impact process as well [5,6]. Shock recovery experiments for calcite yield seemingly conflicting results: early experimental devolatilization studies [7,8,9] suggested that calcite was substantially outgassed at 30 GPa (> 50%). However, the recent petrographic work of [10,11,12] presented evidence that essentially intact calcite is recovered from 60 GPa experiments. [13] reported results of shock experiments on anhydrite, gypsum, and mixtures of those phases with silica. Their observations indicate little or no devolatilization of anhydrite shocked to 42 GPa and that the fraction of sulfur, by mass, that degassed is approx.10(exp -2) of theoretical prediction. In another (preliminary) report of shock experiments on calcite, anhydrite, and gypsum, [14] observe calcite recrystallization when shock loaded at 61 GPa, only intensive plastic deformation in anhydrite shock loaded at 63 GPa, and gypsum converted to anhydrite when shock loaded at 56 GPa. [15] shock loaded anhydrite and quartz to a peak pressure of 60 GPa. All of the quartz grains were trans-formed to glass and the platy anhydrite grains were completely pseudomorphed by small crystallized anhydrite grains. However, no evidence of interaction between the two phases could be observed and they suggest that recrystallization of anhydrite grains is the result of a solid state transformation. [16] reanalyzed the calcite and anhydrite shock

Order–disorder–reorder process in thermally treated dolomite samples

DEFF Research Database (Denmark)

Zucchini, Azzurra; Comodi, Paola; Katerinopoulou, Anna

2012-01-01

A combined powder and single-crystal X-ray diffraction analysis of dolomite [CaMg(CO3)2] heated to 1,200oC at 3 GPa was made to study the order–disorder–reorder process. The order/disorder transition is inferred to start below 1,100oC, and complete disorder is attained at approximately 1,200o......C. Twinned crystals characterized by high internal order were found in samples annealed over 1,100oC, and their fraction was found to increase with temperature. Evidences of twinning domains combined with probable remaining disordered portions of the structure imply that reordering processes occur during...

Inferences of paleoenvironment from petrographic, chemical and stable-isotope studies of calcretes and fracture calcites

International Nuclear Information System (INIS)

Vaniman, D.T.; Whelan, J.F.

1994-01-01

Past research has indicated a genetic connection between calcite formed in calcretes at the surface of Yucca Mountain, Nevada, and calcites deposited in underlying fractures of the unsaturated zone. This common genesis suggests that paleoenvironmental information, as well as the timing and pathways of past recharge episodes, might be obtained from studies of the deposits in both the calcretes and the unsaturated fractures. Chemical and isotopic modification of calcite-precipitating fluids appears to begin at the surface, largely under the influence of plant roots and their decay products. Chemical characteristics of the deeper calcites are either initiated or largely defined within the first few meters of fluid migration into the unsaturated tuffs beneath the calcretes. However, petrographic and isotopic data indicate a very unique low-δ 13 C microenvironment that is localized at the upper surfaces of the calcretes. These surfaces form an interface in the soil horizon where infiltration may pond above the underlying carbonate ''plug.'' In order to decipher the chemistry and petrology of past recharge events, it is important to first understand microenvironments such as this that contribute to mineral precipitation/dissolution events in the pedogenic environment

Influence of Calcite and Dissolved Calcium on Uranium(VI) Sorption to a Hanford Subsurface Sediment

International Nuclear Information System (INIS)

Dong, Wenming; Ball, William P.; Liu, Chongxuan; Wang, Zheming; Stone, Alan T.; Bai, Jing; Zachara, John M.

2005-01-01

The influence of calcite and dissolved calcium on U(VI) adsorption was investigated using a calcite-containing sandy silt/clay sediment from the U. S. Department of Energy Hanford site. U(VI) adsorption to sediment, treated sediment, and sediment size fractions was studied in solutions that both had and had not been preequilibrated with calcite, at initial [U(VI)] ) 10-7-10-5 mol/L and final pH ) 6.0- 10.0. Kinetic and reversibility studies (pH 8.4) showed rapid sorption (30 min), with reasonable reversibility in the 3-day reaction time. Sorption from solutions equilibrated with calcite showed maximum U(VI) adsorption at pH 8.4 (0.1. In contrast, calcium-free systems showed the greatest adsorption at pH 6.0-7.2. At pH > 8.4, U(VI) adsorption was identical from calcium-free and calcium-containing solutions. For calcite-presaturated systems, both speciation calculations and laser-induced fluorescence spectroscopic analyses indicated that aqueous U(VI) was increasingly dominated by Ca2UO2(CO3)3 0(aq) at pH<8.4 and that formation of Ca2UO2(CO3)3 0(aq) is what suppresses U(VI) adsorption. Above pH 8.4, aqueous U(VI) speciation was dominated by UO2(CO3)3 4- in all solutions. Finally, results also showed that U(VI) adsorption was additive in regard to size fraction but not in regard to mineral mass: Carbonate minerals may have blocked U(VI) access to surfaces of higher sorption affinity

Fabrication of calcite blocks from gypsum blocks by compositional transformation based on dissolution-precipitation reactions in sodium carbonate solution.

Science.gov (United States)

Ishikawa, Kunio; Kawachi, Giichiro; Tsuru, Kanji; Yoshimoto, Ayami

2017-03-01

Calcium carbonate (CaCO 3 ) has been used as a bone substitute, and is a precursor for carbonate apatite, which is also a promising bone substitute. However, limited studies have been reported on the fabrication of artificial calcite blocks. In the present study, cylindrical calcite blocks (ϕ6×3mm) were fabricated by compositional transformation based on dissolution-precipitation reactions using different calcium sulfate blocks as a precursor. In the dissolution-precipitation reactions, both CaSO 4 ·2H 2 O and CaSO 4 transformed into calcite, a polymorph of CaCO 3 , while maintaining their macroscopic structure when immersed in 1mol/L Na 2 CO 3 solution at 80°C for 1week. The diametral tensile strengths of the calcite blocks formed using CaSO 4 ·2H 2 O and CaSO 4 were 1.0±0.3 and 2.3±0.7MPa, respectively. The fabrication of calcite blocks using CaSO 4 ·2H 2 O and CaSO 4 proposed in this investigation may be a useful method to produce calcite blocks because of the self-setting ability and high temperature stability of gypsum precursors. Copyright © 2016 Elsevier B.V. All rights reserved.

Mixing of shallow and deep groundwater as indicated by the chemistry and age of karstic springs

Science.gov (United States)

Toth, David J.; Katz, Brian G.

2006-06-01

Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca-HCO3 (six), Na-Cl (four), and mixed (one). The evolution of water chemistry for Ca-HCO3 spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na-Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4-53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (3H), helium-3 (3Hetrit), sulfur hexafluoride (SF6)—for four Ca-HCO3 spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na-Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.

Erratum: Mixing of shallow and deep groundwater as indicated by the chemistry and age of karstic springs

Science.gov (United States)

Toth, David J.; Katz, Brian G.

2006-09-01

Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca-HCO3 (six), Na-Cl (four), and mixed (one). The evolution of water chemistry for Ca-HCO3 spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na-Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4-53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (3H), helium-3 (3Hetrit), sulfur hexafluoride (SF6)—for four Ca-HCO3 spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na-Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.

The Effects of Varying Crustal Carbonate Composition on Assimilation and CO2 Degassing at Arc Volcanoes

Science.gov (United States)

Carter, L. B.; Holmes, A. K.; Dasgupta, R.; Tumiati, S.

2015-12-01

Magma-crustal carbonate interaction and subsequent decarbonation can provide an additional source of CO2 release to the exogenic system superimposed on mantle-derived CO2. Carbonate assimilation at present day volcanoes is often modeled by limestone consumption experiments [1-4]. Eruptive products, however, do not clearly display the characteristic ultracalcic melt compositions produced during limestone-magma interaction [4]. Yet estimated CO2outflux [5] and composition of volcanics in many volcanic systems may allow ~3-17% limestone- or dolostone-assimilated melt contribution. Crystallization may retain ultracalcic melts in pyroxenite cumulates. To extend our completed study on limestone assimilation, here we explore the effect of varying composition from calcite to dolomite on chemical and thermal decarbonation efficiency of crustal carbonates. Piston cylinder experiments at 0.5 GPa and 900-1200 °C demonstrate that residual mineralogy during interaction with magma shifts from CaTs cpx and anorthite/scapolite in the presence of calcite to Di cpx and Fo-rich olivine with dolomite. Silica-undersaturated melts double in magnesium content, while maintaining high (>30 wt.%) CaO values. At high-T, partial thermal breakdown of dolomite into periclase and CO2 is minimal (<5%) suggesting that in the presence of magma, CO2 is primarily released due to assimilation. Assimilated melts at identical P-T conditions depict similarly high volatile contents (10-20 wt.% by EMPA deficit at 0.5 GPa, 1150 °C with hydrous basalt) with calcite or dolomite. Analysis of the coexisting fluid phase indicates the majority of water is dissolved in the melt, while CO2 released from the carbonate is preferentially partitioned into the vapor. This suggests that although assimilated melts have a higher CO2 solubility, most of the CO2can easily degas from the vapor phase at arc volcanoes, possibly more so at volcanic plumbing systems traversing dolomite [8]. [1]Conte et al 2009 EuJMin (21) 763

Dating of aragonite and dolomite from Devil's cave - SP, by dosimetric thermoluminescent method (DTL) and ESR

International Nuclear Information System (INIS)

Tatumi, S.H.

1987-01-01

We have investigated TL (Thermoluminescence) and ESR (electron spin resonance) properties of aragonite and dolomite found at ''Caverna do Diabo (Devil's cave)'' in the state of Sao Paulo to determine the ages of these geological materials. The aragonite, which is not a thermoluminescent material, shows one ESR signal whit g = 2.003. We obtained the age of 1.1 x 10 5 years and the growth rate of 1 μ m/year by the sample calibration with additional Y irradiation. The dolomite gives a TL glow curve with three distinct peaks at 261, 334 and 395 0 C. We found that the fit for the TL glow curve to second-order kinetics can be considerered as very acceptable. Using the second TL peak we obtained the age of 9.4 x 10 5 years and the compatible values of the activation energy (1.90 ± 0,07 eV) by the following methods: Hyperbolic heating, isothermal decay and fractional glow technique. We observed many ESR absorption signals in the dolomite. Three principal signal com g = 2.002, 2.003 and 2.005 were studied. We found that the first and second ESR signals were atributed to the CO 2 - and/or CO 3 3- centers and the last to the CO 3 - centers, and observed that the first ESR signal might related with the second TL peak and the TL sensitivity were associated with the concentration of Mn 2+ [pt

Infrared spectroscopy and density functional theory investigation of calcite, chalk, and coccoliths-do we observe the mineral surface?

DEFF Research Database (Denmark)

Andersson, Martin Peter; Hem, Caroline Piper; Schultz, Logan Nicholas

2014-01-01

broadening from macroscopic dielectric effects. We detect water adsorbed on the high surface area synthetic calcite, which permits observation of the chemistry of thin liquid films on calcite using transmission infrared spectroscopy. The combination of infrared spectroscopy and density functional theory also...... asymmetric for the coccoliths and the synthetic calcite prepared using the carbonation method. It can be very well fitted by two peaks: a narrow Lorenzian at lower frequency and a broader Gaussian at higher frequency. These two samples both have a high specific surface area. Density functional theory...

Journal of Earth System Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

The water quality parameters such as Ca, Mg and HCO3 in the river water suggest under saturation with respect to calcite and dolomite.The mineral stability diagrams indicate that kaolinite and Ca-smectite are stable in the river water environment,hence they occur in suspended sediments and soils.The dominant influence ...

Test of the carbonates structures

International Nuclear Information System (INIS)

Rodriguez, Lidia

1987-01-01

Several samples of carbonates were analyzed by X-ray techniques for determining the crystalline structure of the members of the isomorphes groups of calcite (CaCO 3 ) and dolomite (CaMg(CO 3 ) 2 ). Considering the single crystal, the monocrystal method was used, collecting oscillation and Weissenberg data by means of photographic films. (Author) [es

Reactivity of dolomite in water-saturated supercritical carbon dioxide: Significance for carbon capture and storage and for enhanced oil and gas recovery

International Nuclear Information System (INIS)

Wang Xiuyu; Alvarado, Vladimir; Swoboda-Colberg, Norbert; Kaszuba, John P.

2013-01-01

Highlights: ► Dolomite reactivity with wet and dry supercritical CO 2 were evaluated. ► Dolomite does not react with dry CO 2 . ► H 2 O-saturated supercritical CO 2 dissolves dolomite and precipitates carbonate mineral. ► Temperature/reaction time control morphology and extent of carbonate mineralization. ► Reaction with wet CO 2 may impact trapping, caprock integrity, and CCS/EOR injectivity. - Abstract: Carbon dioxide injection in porous reservoirs is the basis for carbon capture and storage, enhanced oil and gas recovery. Injected carbon dioxide is stored at multiple scales in porous media, from the pore-level as a residual phase to large scales as macroscopic accumulations by the injection site, under the caprock and at reservoir internal capillary pressure barriers. These carbon dioxide saturation zones create regions across which the full spectrum of mutual CO 2 –H 2 O solubility may occur. Most studies assume that geochemical reaction is restricted to rocks and carbon dioxide-saturated formation waters, but this paradigm ignores injection of anhydrous carbon dioxide against brine and water-alternating-gas flooding for enhanced oil recovery. A series of laboratory experiments was performed to evaluate the reactivity of the common reservoir mineral dolomite with water-saturated supercritical carbon dioxide. Experiments were conducted at reservoir conditions (55 and 110 °C, 25 MPa) and elevated temperature (220 °C, 25 MPa) for approximately 96 and 164 h (4 and 7 days). Dolomite dissolves and new carbonate mineral precipitates by reaction with water-saturated supercritical carbon dioxide. Dolomite does not react with anhydrous supercritical carbon dioxide. Temperature and reaction time control the composition, morphology, and extent of formation of new carbonate minerals. Mineral dissolution and re-precipitation due to reaction with water-saturated carbon dioxide may affect the contact line between phases, the carbon dioxide contact angle, and the

The determination of lead, zinc, and magnesium in dolomite and its benefication products by use of x-ray-fluorescence spectrometry

International Nuclear Information System (INIS)

Jacobs, J.J.

1985-01-01

An investigation was undertaken on the development of fast, simple, and accurate methods of analysis for lead and zinc in tailings and middlings from dolomite, and for lead, zinc, and magnesium in concentrates obtained from dolomite. A pressed-powder technique and X-ray-fluorescence spectrometry (XRFS) were used. Good agreement was found between the XRFS values for lead and zinc in low concentrations and the values obtained by other techniques of analysis when the calibration for the XRFS method was effected by the use of synthetic standards comprising lead and zinc oxides in a dolomite matrix. For high concentrations of the analytes, all the oxides and sulphides of lead and zinc in the samples had to be converted to the sulphate form, and a matrix correction had to be applied to the assigned values of the oxide calibration standards. The lower limits of detection for lead, zinc, and magnesium were 0,004, 0,003, and 0,18 per cent respectively. The recommended methods are detailed in two appendices

Geochemical Interaction of Middle Bakken Reservoir Rock and CO2 during CO2-Based Fracturing

Science.gov (United States)

Nicot, J. P.; Lu, J.; Mickler, P. J.; Ribeiro, L. H.; Darvari, R.

2015-12-01

This study was conducted to investigate the effects of geochemical interactions when CO2 is used to create the fractures necessary to produce hydrocarbons from low-permeability Middle Bakken sandstone. The primary objectives are to: (1) identify and understand the geochemical reactions related to CO2-based fracturing, and (2) assess potential changes of reservoir property. Three autoclave experiments were conducted at reservoir conditions exposing middle Bakken core fragments to supercritical CO2 (sc-CO2) only and to CO2-saturated synthetic brine. Ion-milled core samples were examined before and after the reaction experiments using scanning electron microscope, which enabled us to image the reaction surface in extreme details and unambiguously identify mineral dissolution and precipitation. The most significant changes in the reacted rock samples exposed to the CO2-saturated brine is dissolution of the carbonate minerals, particularly calcite which displays severely corrosion. Dolomite grains were corroded to a lesser degree. Quartz and feldspars remained intact and some pyrite framboids underwent slight dissolution. Additionally, small amount of calcite precipitation took place as indicated by numerous small calcite crystals formed at the reaction surface and in the pores. The aqueous solution composition changes confirm these petrographic observations with increase in Ca and Mg and associated minor elements and very slight increase in Fe and sulfate. When exposed to sc-CO2 only, changes observed include etching of calcite grain surface and precipitation of salt crystals (halite and anhydrite) due to evaporation of residual pore water into the sc-CO2 phase. Dolomite and feldspars remained intact and pyrite grains were slightly altered. Mercury intrusion capillary pressure tests on reacted and unreacted samples shows an increase in porosity when an aqueous phase is present but no overall porosity change caused by sc-CO2. It also suggests an increase in permeability

Crystal structure study of a cobaltoan dolomite from Kolwezi, Democratic Republic of Congo

Directory of Open Access Journals (Sweden)

Natale Perchiazzi

2015-03-01

Full Text Available A structural study has been undertaken on a cobaltoan dolomite, with chemical formula CaMg0.83Co0.17(CO32 (calcium magnesium cobalt dicarbonate, from Kolwezi, Democratic Republic of Congo. Pale-pink euhedral cobaltoan dolomite was associated with kolwezite [(Cu1.33Co0.67(CO3(OH2] and cobaltoan malachite [(Cu,Co2(CO3(OH2]. A crystal with a Co:Mg ratio of 1:5.6 (SEM/EDAX measurement, twinned on (11 -2 0 was used for crystal structural refinement. The refinement of the structural model of Reeder & Wenk [Am. Mineral. (1983, 68, 769–776; Ca at site 3a with site symmetry -3; Mg site at site 3b with site symmetry -3; C at site 6c with site symmetry 3; O at site 18f with site symmetry 1] showed that Co is totally incorporated in the Mg site, with refined occupancy Mg0.83Co0.17, which compares with Mg0.85Co0.15 from chemical data. The Co substitution reflects in the expansion of the cell volume, with a pronounced increasing of the c cell parameter.

Diagenesis of Permian alluvial fan deposits of Northern Switzerland

International Nuclear Information System (INIS)

Bluem, W.

1987-01-01

Fine-grained sandstones of Permian alluvial fan deposits from three Nagra boreholes (Weiach, Riniken, Kaisten) and an exploration well, drilled at Wintersingen are clast supported, moderately sorted arkosic greywackes containing typically 2-20 % clayey matrix. Petrographic studies indicate that the origin of this clayey matrix is postdepositional. Mechanical infiltration of fines and diagenetic reddening of detrital and authigenic iron oxides are the earliest recorded events. Additionally, nodular calcites of calcrete origin and fibrous illitic clays are also ascribed to the eogenetic environment. The present strong compaction fabric results from general lack of eogenetic framework supporting cements. During mesogenesis, secondary porosity was generated through partial removal of early calcite. At the same time, a first generation of syntaxial quartz cementation and a subsequent fibrous illite authigenesis took place. Leaching of detrital K-feldspars post-dating compaction is recorded throughout the studied boreholes. The following burial diagenetic events differ between the various boreholes: in Weiach and Wintersingen kaolinite, illite, prismatic quartz and ankerite/siderite are recorded; in Riniken K-feldspar, illite, prismatic quartz and dolomite developed; whilst in Kaisten K-feldspar and microcrystalline quartz-cement dominate. These differences reflect the chemistry, pH and ionic strength of the pore fluids. Filling of veins by dolomite/ankerite, iron-rich and subsequent iron-poor calcite is the latest recorded event. (author) 21 refs., 10 figs., 1 tab

The surface interactions of a near-neutral carbon nanoparticle tracer with calcite

KAUST Repository

Li, Yan Vivian

2016-03-02

A new class of nearly charge-neutral carbon-cored nanoparticle tracers are remarkably non-interactive with solid surfaces and could provide a valuable baseline for diverse hydrological and environmental studies of subsurface flow and particle transport. We investigate the causes of inertness by studying the interactions with calcite of a nanoparticle of this class synthesized from malic acid and ethanolamine (M-dots) dispersed in brine (NaCl, CaCl2, and MgCl2) solutions. None of the M-dots are retained in calcite sand-packed columns when dispersed in DI water. Dispersed in the NaCl and mixed brine solutions, 5.6 % of and 7.3 % of the M-dots are initially retained, but 65 and 13 % of these retained particles are subsequently released when the column is flushed with DI water. When dispersed in the CaCl2 and MgCl2 solutions, 65 and 54 % of the M-dots are initially retained, and 28 and 26 % subsequently released in the DI water flush. The M-dots have a small negative zeta potential in all solutions, but the calcite zeta potential changes from strongly negative to strongly positive across the solution series, and the particle retention tracks this change. Derjaguin–Landau–Verwey–Overbeek (DLVO) modeling of the force between a calcite probe and an M-dot coated surface shows that hydration forces repel the particles in the DI water, NaCl, and mixed solutions, but not in the CaCl2 and MgCl2 solutions. These results show that near-zero charge and strongly hydrophilic decoration are the causes of the remarkable inertness of carbon-cored nanoparticles, and also suggest that nanoparticles could be useful in solute-surface interaction studies.

The surface interactions of a near-neutral carbon nanoparticle tracer with calcite

Energy Technology Data Exchange (ETDEWEB)

Li, Yan Vivian, E-mail: yan.li@colostate.edu [Colorado State University, Department of Design and Merchandising (United States); Cathles, Lawrence M., E-mail: lmc19@cornell.edu [Cornell University, Earth and Atmospheric Sciences (United States)

2016-03-15

A new class of nearly charge-neutral carbon-cored nanoparticle tracers are remarkably non-interactive with solid surfaces and could provide a valuable baseline for diverse hydrological and environmental studies of subsurface flow and particle transport. We investigate the causes of inertness by studying the interactions with calcite of a nanoparticle of this class synthesized from malic acid and ethanolamine (M-dots) dispersed in brine (NaCl, CaCl{sub 2}, and MgCl{sub 2}) solutions. None of the M-dots are retained in calcite sand-packed columns when dispersed in DI water. Dispersed in the NaCl and mixed brine solutions, 5.6 % of and 7.3 % of the M-dots are initially retained, but 65 and 13 % of these retained particles are subsequently released when the column is flushed with DI water. When dispersed in the CaCl{sub 2} and MgCl{sub 2} solutions, 65 and 54 % of the M-dots are initially retained, and 28 and 26 % subsequently released in the DI water flush. The M-dots have a small negative zeta potential in all solutions, but the calcite zeta potential changes from strongly negative to strongly positive across the solution series, and the particle retention tracks this change. Derjaguin–Landau–Verwey–Overbeek (DLVO) modeling of the force between a calcite probe and an M-dot coated surface shows that hydration forces repel the particles in the DI water, NaCl, and mixed solutions, but not in the CaCl{sub 2} and MgCl{sub 2} solutions. These results show that near-zero charge and strongly hydrophilic decoration are the causes of the remarkable inertness of carbon-cored nanoparticles, and also suggest that nanoparticles could be useful in solute-surface interaction studies.Graphical Abstract.

The surface interactions of a near-neutral carbon nanoparticle tracer with calcite

International Nuclear Information System (INIS)

Li, Yan Vivian; Cathles, Lawrence M.

2016-01-01

A new class of nearly charge-neutral carbon-cored nanoparticle tracers are remarkably non-interactive with solid surfaces and could provide a valuable baseline for diverse hydrological and environmental studies of subsurface flow and particle transport. We investigate the causes of inertness by studying the interactions with calcite of a nanoparticle of this class synthesized from malic acid and ethanolamine (M-dots) dispersed in brine (NaCl, CaCl_2, and MgCl_2) solutions. None of the M-dots are retained in calcite sand-packed columns when dispersed in DI water. Dispersed in the NaCl and mixed brine solutions, 5.6 % of and 7.3 % of the M-dots are initially retained, but 65 and 13 % of these retained particles are subsequently released when the column is flushed with DI water. When dispersed in the CaCl_2 and MgCl_2 solutions, 65 and 54 % of the M-dots are initially retained, and 28 and 26 % subsequently released in the DI water flush. The M-dots have a small negative zeta potential in all solutions, but the calcite zeta potential changes from strongly negative to strongly positive across the solution series, and the particle retention tracks this change. Derjaguin–Landau–Verwey–Overbeek (DLVO) modeling of the force between a calcite probe and an M-dot coated surface shows that hydration forces repel the particles in the DI water, NaCl, and mixed solutions, but not in the CaCl_2 and MgCl_2 solutions. These results show that near-zero charge and strongly hydrophilic decoration are the causes of the remarkable inertness of carbon-cored nanoparticles, and also suggest that nanoparticles could be useful in solute-surface interaction studies.Graphical Abstract

Principles of calcite dissolution in human and artificial otoconia.

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Leif Erik Walther

Full Text Available Human otoconia provide mechanical stimuli to deflect hair cells of the vestibular sensory epithelium for purposes of detecting linear acceleration and head tilts. During lifetime, the volume and number of otoconia are gradually reduced. In a process of degeneration morphological changes occur. Structural changes in human otoconia are assumed to cause vertigo and balance disorders such as benign paroxysmal positional vertigo (BPPV. The aim of this study was to investigate the main principles of morphological changes in human otoconia in dissolution experiments by exposure to hydrochloric acid, EDTA, demineralized water and completely purified water respectively. For comparison reasons artificial (biomimetic otoconia (calcite gelatin nanocomposits and natural calcite were used. Morphological changes were detected in time steps by the use of environmental scanning electron microscopy (ESEM. Under in vitro conditions three main dissolution mechanisms were identified as causing characteristic morphological changes of the specimen under consideration: pH drops in the acidic range, complex formation with calcium ions and changes of ion concentrations in the vicinity of otoconia. Shifts in pH cause a more uniform reduction of otoconia size (isotropic dissolution whereas complexation reactions and changes of the ionic concentrations within the surrounding medium bring about preferred attacks at specific areas (anisotropic dissolution of human and artificial otoconia. Owing to successive reduction of material, all the dissolution mechanisms finally produce fragments and remnants of otoconia. It can be assumed that the organic component of otoconia is not significantly attacked under the given conditions. Artificial otoconia serve as a suitable model system mimicking chemical attacks on biogenic specimens. The underlying principles of calcite dissolution under in vitro conditions may play a role in otoconia degeneration processes such as BPPV.

Galacturonomannan and Golgi-derived membrane linked to growth and shaping of biogenic calcite

Science.gov (United States)

Marsh, M. E.; Ridall, A. L.; Azadi, P.; Duke, P. J.

2002-01-01

The coccolithophores are valuable models for the design and synthesis of composite materials, because the cellular machinery controlling the nucleation, growth, and patterning of their calcitic scales (coccoliths) can be examined genetically. The coccoliths are formed within the Golgi complex and are the major CaCO(3) component in limestone sediments-particularly those of the Cretaceous period. In this study, we describe mutants lacking a sulfated galacturonomannan and show that this polysaccharide in conjunction with the Golgi-derived membrane is directly linked to the growth and shaping of coccolith calcite but not to the initial orientated nucleation of the mineral phase.

Strontium, nickel, cadmium, and lead substitution into calcite, studied by density functional theory

DEFF Research Database (Denmark)

Andersson, Martin Peter; Sakuma, Hiroshi; Stipp, Susan Louise Svane

2014-01-01

We have used density functional theory to predict the ion exchange energies for divalent cations Ni(2+), Sr(2+), Cd(2+), and Pb(2+) into a calcite {10.4} surface in equilibrium with water. Exchange energies were calculated for substitution into the topmost surface layer, at the mineral-fluid inte......We have used density functional theory to predict the ion exchange energies for divalent cations Ni(2+), Sr(2+), Cd(2+), and Pb(2+) into a calcite {10.4} surface in equilibrium with water. Exchange energies were calculated for substitution into the topmost surface layer, at the mineral...

Strontium isotope evolution of pore water and calcite in the Topopah Spring Tuff, Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Marshall, Brian D.; Futa, Kiyoto

2001-01-01

Pore water in the Topopah Spring Tuff has a narrow range of (delta) 87 Sr values that can be calculated from the (delta) 87 Sr values of the rock considering advection through and reaction with the overlying nonwelded tuffs of the PTn. This model can be extended to estimate the variation of (delta) 87 Sr in the pore water through time; this approximates the variation of (delta) 87 Sr measured in calcite fracture coatings. In samples of calcite where no silica can be dated by other methods, strontium isotope data may be the only method to determine ages. In addition, other Sr-bearing minerals in the calcite and opal coatings, such as fluorite, may be dated using the same model

MicroCT vs. Hg porosimetry: microporosity in commercial stones

Science.gov (United States)

Fusi, N.; Martinez-Martinez, J.; Barberini, V.; Galimberti, L.

2009-04-01

Decay of rocks, due both to extrinsic and intrinsic factors, can show up in several different forms, such as neoformation of minerals, decohesion of grains and/or crystals, magnification of previous defects, new discontinuities, etc. Intrinsic factors include the type of material, its properties and microstructure, in particular porosity and microporosity. Extrinsic factors relate to atmosphere and usage of the material itself. Rock degradation has several heavy consequences for commercial stones, such as increase of permeability, loss of material, loss of mechanical strength; these consequences are of crucial importance for conservation of historical buildings. Aim of this study is to compare microporosity of some massive commercial stones by means of X ray microtomography, a non destructive technique, and Hg porosimetry. Nine of the most used Spanish limestones and dolostones have been analysed. The lithotypes have been chosen for their homogeneous mineralogical composition (calcitic or dolomitic) and for their low porosity; some of them have been widely used in Spain for historical buildings. Different lithotypes have been described in thin section: Ambarino (A) and Beige Serpiente (BS): brecciated dolostone, composed by microcrystalline dolomitic clasts, in a dolomitic and/or calcitic microcrystalline matrix. Amarillo Triana (AT): yellow dolomitic marble, with fissures filled up by calcite and Fe oxides. Blanco Alconera (BA): a white-pink homogeneous limestone, with veins. Blanco Tranco (BT): a homogeneous white calcitic marble, without any fissures and/or fractures. Crema Valencia (CV): a pinkish limestone, characterized by abundant stilolythes, filled mainly by quartz (80%) and kaolin (11%). Gris Macael (GM): a calcitic marble wiht darker and lighter beds, conferring a strong anisotropy. Rojo Cehegin (RC): a red fossiliferous limestone with white calcitic veins. Travertino Blanco (TB): a massive white calcitic travertine. Prismatic samples of about 2x1x1 cm

Full-scale laboratory drilling tests on sandstone and dolomite. Final report

Energy Technology Data Exchange (ETDEWEB)

Black, A. D.; Green, S. J.; Rogers, L. A.

1977-08-01

Full-scale laboratory drilling experiments were performed under simulated downhole conditions to determine what effect changing various drilling parameters has on penetration rate. The two rock types, typical of deep oil and gas reservoirs, used for the tests were Colton Sandstone and Bonne Terre Dolomite. Drilling was performed with standard 7/sup 7///sub 8/ inch rotary insert bits and water base mud. The results showed the penetration rate to be strongly dependent on bit weight, rotary speed and borehole mud pressure. There was only a small dependence on mud flow rate. The drilling rate decreased rapidly with increasing borehole mud pressure for borehole pressures up to about 2,000 psi. Above this pressure, the borehole pressure and rotary speeds had a smaller effect on penetration rate. The penetration rate was then dependent mostly on the bit weight. Penetration rate per horsepower input was also shown to decrease at higher mud pressures and bit weights. The ratio of horizontal confining stress to axial overburden stress was maintained at 0.7 for simulated overburden stresses between 0 and 12,800 psi. For this simulated downhole stress state, the undrilled rock sample was within the elastic response range and the confining pressures were found to have only a small or negligible effect on the penetration rate. Visual examination of the bottomhole pattern of the rocks after simulated downhole drilling, however, revealed ductile chipping of the Sandstone, but more brittle behavior in the Dolomite.

Rapid stepwise onset of Antarctic glaciation and deeper calcite compensation in the Pacific Ocean.

Science.gov (United States)

Coxall, Helen K; Wilson, Paul A; Pälike, Heiko; Lear, Caroline H; Backman, Jan

2005-01-06

The ocean depth at which the rate of calcium carbonate input from surface waters equals the rate of dissolution is termed the calcite compensation depth. At present, this depth is approximately 4,500 m, with some variation between and within ocean basins. The calcite compensation depth is linked to ocean acidity, which is in turn linked to atmospheric carbon dioxide concentrations and hence global climate. Geological records of changes in the calcite compensation depth show a prominent deepening of more than 1 km near the Eocene/Oligocene boundary (approximately 34 million years ago) when significant permanent ice sheets first appeared on Antarctica, but the relationship between these two events is poorly understood. Here we present ocean sediment records of calcium carbonate content as well as carbon and oxygen isotopic compositions from the tropical Pacific Ocean that cover the Eocene/Oligocene boundary. We find that the deepening of the calcite compensation depth was more rapid than previously documented and occurred in two jumps of about 40,000 years each, synchronous with the stepwise onset of Antarctic ice-sheet growth. The glaciation was initiated, after climatic preconditioning, by an interval when the Earth's orbit of the Sun favoured cool summers. The changes in oxygen-isotope composition across the Eocene/Oligocene boundary are too large to be explained by Antarctic ice-sheet growth alone and must therefore also indicate contemporaneous global cooling and/or Northern Hemisphere glaciation.

Diagenetic history of the Swan Hills Simonette Oil Reservoir (Givetian-Frasnian), deep basin of west-central Alberta, Canada

Energy Technology Data Exchange (ETDEWEB)

Duggan, J.P.; Mountjoy, E.W. [McGill Univ., Montreal, PQ (Canada). Dept. of Earth and Planetary Sciences

1997-05-01

The geology and diagenetic history of the Swan Hills Simonette oil field of west-central Alberta basin was described. Present-day burial depth is 3900 m; formation temperature is 93 degrees C. Highest porosites (20 per cent) occur in dolostones of the lagoon, ref, and fore-reef depositional environments but limestones still retain porosities up to five per cent. Hydrocarbons are present in saddle dolomite fluid inclusions. Oxygen isotopes for replacement dolomites and late calcite suggest that the carbonate-precipitating fluids were derived from the Precambrian basement or Paleozoic clastics sourced from the basement. Faults may have acted as vertical conduits for fluid migration.

Removal of trace elements from landfill leachate by calcite precipitation

Czech Academy of Sciences Publication Activity Database

Ettler, V.; Zelená, O.; Mihaljevič, M.; Šebek, O.; Strnad, L.; Coufal, P.; Bezdička, Petr

2006-01-01

Roč. 88, 1-3 (2006), s. 28-31 ISSN 0375-6742 R&D Projects: GA AV ČR(CZ) KJB3111402 Institutional research plan: CEZ:AV0Z40320502 Keywords : landfill leachate * calcite * scavenging Subject RIV: CA - Inorganic Chemistry Impact factor: 0.922, year: 2006

Calcite microcrystals in the pineal gland of the human brain: second harmonic generators and possible piezoelectric transducers

International Nuclear Information System (INIS)

Lang, S.B.

2004-01-01

Full text: A new form of biomineralization in the pineal gland of the human brain has been studied. It consists of small crystals that are less than 20 μm in length and that are completely distinct from the often-observed mulberry-type hydroxyapatite concretions. Cubic, hexagonal and cylindrical morphologies have been identified using scanning electron microscopy. Energy dispersive spectroscopy, selected-area electron diffraction and near infrared Raman spectroscopy established that the crystals were calcite. Experiments at the European Synchrotron Radiation Facility (ESRF) to study the biomineralization showed the presence of sulfur originating from both sugars and proteins. Other studies at the ESRF furnished information on the complex texture crystallization of the calcite. With the exception of the otoconia structure of the inner ear, this is the only known non-pathological occurrence of calcite in the human body. The calcite microcrystals are believed to be responsible for the previously observed second harmonic generation (SHG) in pineal tissue sections. There is a strong possibility that the complex twinned structure of the crystals may lower their symmetry and permit the existence of a piezoelectric effect

Amino Acid-Assisted Incorporation of Dye Molecules within Calcite Crystals.

Science.gov (United States)

Marzec, Bartosz; Green, David C; Holden, Mark A; Coté, Alexander S; Ihli, Johannes; Khalid, Saba; Kulak, Alexander; Walker, Daniel; Tang, Chiu; Duffy, Dorothy M; Kim, Yi-Yeoun; Meldrum, Fiona C

2018-05-23

Biomineralisation processes invariably occur in the presence of multiple organic additives, which act in combination to give exceptional control over structures and properties. However, few synthetic studies have investigated the cooperative effects of soluble additives. This work addresses this challenge and focuses on the combined effects of amino acids and coloured dye molecules. The experiments demonstrate that strongly coloured calcite crystals only form in the presence of Brilliant Blue R (BBR) and four of the seventeen soluble amino acids, as compared with almost colourless crystals using the dye alone. The active amino acids are identified as those which themselves effectively occlude in calcite, suggesting a mechanism where they can act as chaperones for individual molecules or even aggregates of dyes molecules. These results provide new insight into crystal-additive interactions and suggest a novel strategy for generating materials with target properties. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Krypton-81 in groundwater of the Culebra Dolomite near the Waste Isolation Pilot Plant, New Mexico.

Science.gov (United States)

Sturchio, Neil C; Kuhlman, Kristopher L; Yokochi, Reika; Probst, Peter C; Jiang, Wei; Lu, Zheng-Tian; Mueller, Peter; Yang, Guo-Min

2014-05-01

The Waste Isolation Pilot Plant (WIPP) in New Mexico is the first geologic repository for disposal of transuranic nuclear waste from defense-related programs of the US Department of Energy. It is constructed within halite beds of the Permian-age Salado Formation. The Culebra Dolomite, confined within Rustler Formation evaporites overlying the Salado Formation, is a potential pathway for radionuclide transport from the repository to the accessible environment in the human-disturbed repository scenario. Although extensive subsurface characterization and numerical flow modeling of groundwater has been done in the vicinity of the WIPP, few studies have used natural isotopic tracers to validate the flow models and to better understand solute transport at this site. The advent of Atom-Trap Trace Analysis (ATTA) has enabled routine measurement of cosmogenic (81)Kr (half-life 229,000 yr), a near-ideal tracer for long-term groundwater transport. We measured (81)Kr in saline groundwater sampled from two Culebra Dolomite monitoring wells near the WIPP site, and compared (81)Kr model ages with reverse particle-tracking results of well-calibrated flow models. The (81)Kr model ages are ~130,000 and ~330,000 yr for high-transmissivity and low-transmissivity portions of the formation, respectively. Compared with flow model results which indicate a relatively young mean hydraulic age (~32,000 yr), the (81)Kr model ages imply substantial physical attenuation of conservative solutes in the Culebra Dolomite and provide limits on the effective diffusivity of contaminants into the confining aquitards. Copyright © 2014 Elsevier B.V. All rights reserved.

The review of recent carbonate minerals processing technology

Science.gov (United States)

Solihin

2018-02-01

Carbonate is one of the groups of minerals that can be found in relatively large amount in the earth crust. The common carbonate minerals are calcium carbonate (calcite, aragonite, depending on its crystal structure), magnesium carbonate (magnesite), calcium-magnesium carbonate (dolomite), and barium carbonate (barite). A large amount of calcite can be found in many places in Indonesia such as Padalarang, Sukabumi, and Tasikmalaya (West Java Provence). Dolomite can be found in a large amount in Gresik, Lamongan, and Tuban (East Java Provence). Magnesite is quite rare in Indonesia, and up to the recent years it can only be found in Padamarang Island (South East Sulawesi Provence). The carbonate has been being exploited through open pit mining activity. Traditionally, calcite can be ground to produce material for brick production, be carved to produce craft product, or be roasted to produce lime for many applications such as raw materials for cement, flux for metal smelting, etc. Meanwhile, dolomite has traditionally been used as a raw material to make brick for local buildings and to make fertilizer for coconut oil plant. Carbonate minerals actually consist of important elements needed by modern application. Calcium is one of the elements needed in artificial bone formation, slow release fertilizer synthesis, dielectric material production, etc. Magnesium is an important material in automotive industry to produce the alloy for vehicle main parts. It is also used as alloying element in the production of special steel for special purpose. Magnesium oxide can be used to produce slow release fertilizer, catalyst and any other modern applications. The aim of this review article is to present in brief the recent technology in processing carbonate minerals. This review covers both the technology that has been industrially proven and the technology that is still in research and development stage. One of the industrially proven technologies to process carbonate mineral is

Porosity development in the Copper Ridge Dolomite and Maynardville Limestone, Bear Creek Valley and Chestnut Ridge, Tennessee

International Nuclear Information System (INIS)

Goldstrand, P.M.; Menefee, L.S.; Dreier, R.B.

1995-12-01

Matrix porosity data from deep core obtained in Bear Creek Valley indicate that porosities in the Maynardville Limestone are lithology and depth dependent. Matrix porosities are greater in the Cooper Ridge Dolomite than in the Maynardville Limestone, yet there is no apparent correlation with depth. Two interrelated diagenetic processes are the major controlling factors on porosity development in the Copper Ridge Dolomite and Maynardville Limestone; dissolution of evaporate minerals and dedolomitization. Both of these diagenetic processes produce matrix porosities between 2.1 and 1.3% in the Copper Ridge Dolomite and upper part of the Maynardville Limestone (Zone 6) to depths of approximately 600 ft bgs. Mean matrix porosities in Zones 5 through 2 of the Maynardville Limestone range from 0.8 to 0.5%. A large number of cavities have been intersected during drilling activities in nearly all zones of the Maynardville Limestone in Bear Creek Valley. Therefore, any maynardville Limestone zone within approximately 200 ft of the ground surface is likely to contain cavities that allow significant and rapid flow of groundwater. Zone 6 could be an important stratigraphic unit in the Maynardville Limestone for groundwater flow and contaminant transport because of the abundance of vuggy and moldic porosities. There are large variations in the thickness and lithology in the lower part of the Maynardville (Zones 2, 3, and 4 in the Burial Grounds region). The direction and velocity of strike-parallel groundwater flow may be altered in this area within the lower Maynardville Limestone

Facies-controlled reservoir properties in ramp-fan and slope-apron deposits, Miocene Puente Formation, Los Angeles basin

Energy Technology Data Exchange (ETDEWEB)

Lyons, K.T.; Geving, R.L.; Suchecki, R.K.

1989-03-01

The Miocene Puente Formation in outcrops of the eastern Los Angeles basin is interpreted as a succession of slope-apron and ramp-fan deposits that accumulated in a prism-rise wedge. The principal depositional components of this dominantly base-of-slope and ramp system are ramp-fan channels and lobes, and slope-channel and slope-apron channel/interchannel deposits. Facies-specific textural, compositional, and diagenetic attributes observed in thin section assist in the classification of depositional facies. Specifically, occurrence of carbonate cement, clay mineralogy, and abundance of organic material vary as a function of component facies architecture of the depositional system. Slope and ramp-fan channel-fill sandstones are characterized by pervasive carbonate cements, including poikilotopic and fine-grained calcite, fine-grained and baroque dolomite, and minor siderite. Diagenetic clays predate carbonate cements, and dolomite predates coarser, void-filling calcite. Ramp-fan lobe and interchannel deposits are carbonate free but are rich in detrital clay and organic matter. Diagenetic clays include mixed-layer illite/smectite and kaolinite. Sediments deposited in slope-apron channel fill are virtually cement free except for small amounts of authigenic illite/smectite. Slope-apron interchannel deposits are characterized by high content of organic matter and clay-rich matrix. Potential reservoir characteristics, such as grain size, sorting, and abundance of depositional clay matrix, are related to the primary sedimentary properties of depositional architectural components in the ramp-fan and slope-apron system. Additional diagenetic modifications, without consideration of compaction, were controlled by precipitation reactions associated with fluid flow along pathways related to the depositional architectural framework.

Effect of SO2 Dry Deposition on Porous Dolomitic Limestones

Directory of Open Access Journals (Sweden)

Florica Doroftei

2010-01-01

Full Text Available The present study is concerned with the assessment of the relative resistance of a monumental dolomitic limestone (Laspra – Spain used as building material in stone monuments and submitted to artificial ageing by SO2 dry deposition in the presence of humidity. To investigate the protection efficiency of different polymeric coatings, three commercially available siloxane-based oligomers (Lotexan-N, Silres BS 290 and Tegosivin HL 100 and a newly synthesized hybrid nanocomposite with silsesquioxane units (TMSPMA were used. A comparative assessment of the data obtained in this study underlines that a better limestone protection was obtained when treated with the hybrid nanocomposite with silsesquioxane units.

Fluid inclusion studies of calcite veins from Yucca Mountain, Nevada, Tuffs: Environment of formation

Energy Technology Data Exchange (ETDEWEB)

Roedder, E. [Harvard Univ., Cambridge, MA (United States); Whelan, J.F. [Geological Survey, Denver, CO (United States); Vaniman, D.T. [Los Alamos National Lab., NM (United States)

1994-12-31

Calcite vein and vug fillings at four depths (130-314m), all above the present water table in USW G-1 bore hole at Yucca Mountain, Nevada, contain primary fluid inclusions with variable vapor/liquid raitos: Most of these inclusions are either full of liquid or full of vapor. The liquid-filled inclusions show that most of the host calcite crystallized from fluids at <100{degrees}C. The vapor-filled inclusions provide evidence that a separate vapor phase was present in the fluid during crystallization. Studies of these vapor-filled inclusions on the microscope crushing stage were interpreted in an earlier paper as indicating trapping of an air-water-CO{sub 2} vapor phase at ``<100{degrees}C``. Our new studies reveal the additional presence of major methane in the vapor-filled inclusion, indicating even lower temperatures of trapping, perhaps at near-surface temperatures. They also show that the host calcite crystals grew from a flowing film of water on the walls of fractures open to the atmosphere, the vapor-filled inclusions representing bubbles that exsolved from this film onto the crystal surface.

Molecular dynamics simulations of the calcite/solution interface as a means to explore surface modifications induced by nitrate

Energy Technology Data Exchange (ETDEWEB)

Hofmann, Sascha; Schmidt, Moritz [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Div. Surface Processes; Spijker, P. [Aalto Univ., Helsinki (Finland). Dept. of Applied Physics; Voitchovsky, K. [Durham Univ. (United Kingdom). Physics Dept.

2016-07-01

The reactivity of calcite, one of the most abundant minerals in the earth's crust, is determined by the molecular details of its interface with the contacting solution. Recently, it has been found that trace concentrations of NaNO{sub 3} severely affect calcite's (104) surface and its reactivity. Molecular dynamics (MD) simulations reveal density profiles of different ions near calcite's surface, with NO{sub 3}{sup -} able to reach closer to the surface than CO{sub 3}{sup 2-} and in higher concentrations. Additionally, incorporation of NO{sub 3}{sup -} into the surface significantly disturbs the water structure at the interface.

The genesis of the ore hosting 'dolomitic marble' in the Bayan Obo deposit, Inner Mongolia, China: constrained by isotopic results

International Nuclear Information System (INIS)

Ding Tiping; Tian Shihong; Wang Defang; Jiang Shaoyong; Bai Ruimei

2003-01-01

The Bayan Obo Fe-REE-Nb ore deposit, Inner Mongolia, China is a super large REE deposit. This deposit attracts attentions of many geologists and geochemists for its unique geological characters and geotectonic background. However, there are quite a number of controversies on various aspects of its genesis, such as when the ore deposit was formed, where the ore forming materials came from and what conditions and geotectonic environment the deposit was formed. Among them, the genesis of ore bearing 'dolomitic marble' is a focus point of debating. isotopic methods are important tools for study on ore deposits. Therefore, supplemental stable isotope investigation was undertaken in this study to reach more information on the forming conditions of 'dolomitic marble'. The high contents of REE and Nb, the REE distribution pattern, the low initial 87 Sr/ 86 Sr ratio and low δ 30 Si values of trace silica in 'dolomitic marble' all indicate its magmatic origin. The high δ 18 O values of carbonate and silicate minerals, and the relatively high δ 34 S values indicate that this rock had experienced isotopic exchange with sea water, implying their submarine volcanic origin. The δ 13 C values observed in carbonate and silicate minerals can also be explained by carbonatite assimilated by oceanic carbonate. Therefore, based on its isotopic characters, the 'dolomitic marble' is more likely of volcanic carbonatite rock formed during middle Proterozoic era. (authors)

Petro-structural, geochemical and carbon and oxygen isotopic study on carbonates crosscuting the Oman Ophiolite peridotites: evidence of polygenic CO2 trapping

Science.gov (United States)

Noël, J.; Godard, M.; Martinez, I.; Oliot, E.; Williams, M. J.; Rodriguez, O.; Chaduteau, C.; Gouze, P.

2017-12-01

Carbon trapping in ophiolitic peridotites contributes to the global carbon cycle between solid Earth and its outer envelopes (through subduction and/or modern alteration). To investigate this process, we performed petro-structural (microtomography, EBSD, EPMA) and geochemical studies (LA-ICP-MS, carbon and oxygen isotopes on bulk and minerals using SHRIMP) of harzburgites cored in the Oman Ophiolite. Studied harzburgites are highly serpentinized (> 90 %) and crosscut by 3 generations of carbonates (> 20 Vol%) with compositions from calcite to dolomite (Mg/Ca = 0-0.85). Type 1 carbonates are fine penetrative veinlets and mesh core after olivine. They have low REE (e.g., Yb = 0.08-0.23 x CI-chondrite) and negative Ce anomalies. They have δ13CPDB = -15.2 to 1.10‰ and δ18OSMOW = 17.5 to 33.7‰, suggesting precipitation temperatures up to 110°C. Type 2 carbonates are pluri-mm veins bounded by cm-thick serpentinized vein selvages, oriented dominantly parallel to mantle foliation. Dynamic recrystallization is observed, indicating polygenetic formation: well crystallized calcite with REE abundances similar to Type 1 carbonates are locally replaced by small dolomite and calcite grains with higher REE (e.g., Yb = 0.35-1.0 x CI-chondrite) and positive Gd anomaly. Type 2 carbonates have δ13CPDB = -12.6 to -4.1‰ and δ18OSMOW = 25.0 to 32.7‰, suggesting precipitation temperatures from 10 to 60°C. Type 3 carbonates are late pluri-mm to cm veins reactivating Type 2 veins. They consist of small grains of dolomite and calcite with REE abundances similar to recrystallized Type 2 carbonates. Type 3 carbonates have δ13CPDB = -8.3 to -5.8‰ and δ18OSMOW = 28.8 to 32.7‰, suggesting precipitation temperatures 100°C). Formation of carbonate veins (Type 2) indicates localization of fluid flux, while serpentinization remains the dominant alteration process. Low T carbonate veins (Type 3) remain the main flow path through ophiolitic peridotites. Our study suggests that

Mineral contents and their solubility on calcium carbonat calcite nanocrystals from cockle shell powder (Anadara granosa Linn)

Science.gov (United States)

Widyastuti, S.; Pramushinta, I. A.

2018-03-01

Prepared and characterized calcium carbonat calcite nanocrystals improves solubility. Calcium carbonat calcite nanocrystals were synthesized using precipitation method from the waste of blood clam cockle shells (Anadara granosa Linn). This study was conducted to analyze mineral composition of nanocrystals calcium carbonat calcite cockle (Anadara granosa) shell for calcium fortification of food applications and to evaluate the solubilities of Calsium and Phospor. The sample of nanocrystals from cockle shells was evaluated to determine the content of 11 macro-and micro-elements. These elements are Calcium (Ca), Magnesium (Mg), Sodium (Na), Phosphorus (P), Potassium (K), Ferrum (Fe), Copper (Cu), Nickel (Ni), Zink (Zn), Boron (B) and Silica (Si)). Cockleshell powders were found to contain toxic elements below detectable levels. The solubilities of Calcium and Phospor were p<0.05.

POTENTIALLY UNSTABLE SLOPE ABOVE ORE PROCESSING PLANT IN THE "OČURA" DOLOMITE QUARRY (LEPOGLAVA, NORTH CROATIA

Directory of Open Access Journals (Sweden)

Karlo Braun

1993-12-01

Full Text Available The complex engineering investigation, in the nearest surroun-dig of the conditionally stable high slope, close to ore processing facilities in the dolomite quarry »Očura« near Lepoglava (North Croatia, was carried out. Studying the tectonic features of the rock mass, discontinuities referent to the slope stability, was found out. Rock fragment size was measured and data processed using statistical design. According to rock fragment mean values, velocity of the longitudinal seismic waves was predicted. This values was compared with velocities of the longitudinal seismic waves, determined using gcophisical refraction seismic method. Physical and mechanical properties of the dolomite rock mass, considering longitudinal and transversal seismic wave velocities, and »RMR«-classification was assesed. All the results indicate, that the slope above the ore processing facilities should be consider as conditionally stable, with real probability to get unstable under the vibrations caused by blasting, during the exploitation in the field, close behind the investigated slope (the paper is published in Croatian.

Molecular models of alginic acid: Interactions with calcium ions and calcite surfaces

Science.gov (United States)

Perry, Thomas D.; Cygan, Randall T.; Mitchell, Ralph

2006-07-01

Cation binding by polysaccharides is observed in many environments and is important for predictive environmental modeling, and numerous industrial and food technology applications. The complexities of these cation-organic interactions are well suited for predictive molecular modeling and the analysis of conformation and configuration of polysaccharides and their influence on cation binding. In this study, alginic acid was chosen as a model polymer system and representative disaccharide and polysaccharide subunits were developed. Molecular dynamics simulation of the torsion angles of the ether linkage between various monomeric subunits identified local and global energy minima for selected disaccharides. The simulations indicate stable disaccharide configurations and a common global energy minimum for all disaccharide models at Φ = 274 ± 7°, Ψ = 227 ± 5°, where Φ and Ψ are the torsion angles about the ether linkage. The ability of disaccharide subunits to bind calcium ions and to associate with the (101¯4) surface of calcite was also investigated. Molecular models of disaccharide interactions with calcite provide binding energy differences for conformations that are related to the proximity and residence densities of the electron-donating moieties with calcium ions on the calcite surface, which are controlled, in part, by the torsion of the ether linkage between monosaccharide units. Dynamically optimized configurations for polymer alginate models with calcium ions were also derived.

Polygenetic Karsted Hardground Omission Surfaces in Lower Silurian Neritic Limestones: a Signature of Early Paleozoic Calcite Seas

Science.gov (United States)

James, Noel P.; Desrochers, André; Kyser, Kurt T.

2015-04-01

Exquisitely preserved and well-exposed rocky paleoshoreline omission surfaces in Lower Silurian Chicotte Formation limestones on Anticosti Island, Quebec, are interpreted to be the product of combined marine and meteoric diagenesis. The different omission features include; 1) planar erosional bedding tops, 2) scalloped erosional surfaces, 3) knobs, ridges, and swales at bedding contacts, and 4) paleoscarps. An interpretation is proposed that relates specific omission surface styles to different diagenetic-depositional processes that took place in separate terrestrial-peritidal-shallow neritic zones. Such processes were linked to fluctuations in relative sea level with specific zones of diagenesis such as; 1) karst corrosion, 2) peritidal erosion, 3) subtidal seawater flushing and cementation, and 4) shallow subtidal deposition. Most surfaces are interpreted to have been the result of initial extensive shallow-water synsedimentary lithification that were, as sea level fell, altered by exposure and subaerial corrosion, only to be buried by sediments as sea level rose again. This succession was repeated several times resulting in a suite of recurring polyphase omission surfaces through many meters of stratigraphic section. Synsedimentary cloudy marine cements are well preserved and are thus interpreted to have been calcitic originally. Aragonite components are rare and thought to have to have been dissolved just below the Silurian seafloor. Large molluscs that survived such seafloor removal were nonetheless leached and the resultant megamoulds were filled with synsedimentary calcite cement. These Silurian inner neritic-strandline omission surfaces are temporally unique. They are part of a suite of marine omission surfaces that are mostly found in early Paleozoic neritic carbonate sedimentary rocks. These karsted hardgrounds formed during a calcite-sea time of elevated marine carbonate saturation and extensive marine cement precipitation. The contemporaneous greenhouse

Origin of calcite in the glacigenic Virttaankangas complex

OpenAIRE

Nina M. Kortelainen; Petri J. Korkeakoski; Juha A. Karhu

2007-01-01

Groundwaters of the glacigenic Virttaankangas complex in southern Finland are characterized by high pH values ranging up to 9.5. These values are significantly higher than those observed in silicate-rich shallow groundwater formations in crystalline bedrock areas. TheVirttaankangas sediments were discovered to contain small amounts of fine grained, dispersed calcite, which has a high tendency to increase the pH of local groundwaters. The primary goal of this study was to determine the mode of...

Smaller calcite lattice deformation caused by occluded organic material in coccoliths than in mollusk shell

DEFF Research Database (Denmark)

Frølich, Simon; Sørensen, Henning Osholm; Hakim, Sepideh Sadat

2015-01-01

The growth and nucleation of biominerals are directed and affected by associated biological molecules. In this paper, we investigate the influence of occluded biomolecules on biogenic calcite from the coccolithophorid Pleurochrysis carterae and from chalk, a rock composed predominantly of fossil....... Two heating cycles allow us to differentiate the effects of thermal agitation and organic molecules. Single peak analysis and Rietveld refinement were combined to show significant differences resulting from the occluded biomolecules on the mineral phase in biogenic calcite in the mollusk shell...

Effects of Citrate and Arginine on Sorption of Nickel to Yazd Sepiolite and Calcite

Directory of Open Access Journals (Sweden)

Ahmadreza Sheikhhosseini

2017-03-01

Full Text Available Introduction: Pollution of soil and water environment by release of heavy metals is of great concerns of the last decades. Sorption of heavy metals by low cost materials is considered as an inexpensive and efficient method used for removal of heavy metals from soil-water systems. The presence of different ligands with various complexing abilities can change the sorption properties of heavy metals and their fate in the environment as well. In order to assess the effect of citrate and arginine as natural organic ligands in soil environment, in a batch study we investigated the effects of these ligands on equilibrium sorption of nickel to sepiolite and calcite minerals and also kinetics of Ni sorption by these minerals. Materials and Methods: Minerals used in this study included sepiolite from Yazd (Iran and pure calcite (Analytical grade, Merck, Germany. Sepiolite was purified, saturated with Ca using 0.5 M CaCl2, powdered in a mortar and sieved by non-metal 230 mesh standard wire sieve. For equilibrium sorption study, in a 50-mL polyethylene centrifuge tube,0.3 g sample of each mineral was suspended in 30 mL of a 0.01 M CaCl2 solution containing 0, 5, 10, 20, 40, 60, 80 and 100 mg L-1 Ni (NiCl2 and containing zero (as control or 0.1mmol L-1 citrate or arginine ligands. The applied concentrationsfor each ligand can naturally occur in soils. Preparedtubes were shaken (180±2 rpm, 25±1oC for 24 h using an orbital shaker and centrifuged (4000×g for 10 min and the supernatants were analyzed for Ni concentration using an atomic absorption spectrophotometer (AAnalyst 200 Perkin-Elmer at a wavelength of 232 nm and a detection limit of 0.05 mg L-1. The quantity of Ni retained by each mineral at equilibrium was calculated using equation qe = (Ci - CeV/W where qe was the amount of nickel retained by mineral surface at equilibrium. Ci and Ce were the initial and the equilibrium concentrations (mg L-1 of Ni, respectively, V was the volume (L of the solution

Summary of Research through Phase II/Year 2 of Initially Approved 3 Phase/3 Year Project - Establishing the Relationship between Fracture-Related Dolomite and Primary Rock Fabric on the Distribution of Reservoirs in the Michigan Basin

Energy Technology Data Exchange (ETDEWEB)

G. Grammer

2007-09-30

This final scientific/technical report covers the first 2 years (Phases I and II of an originally planned 3 Year/3 Phase program). The project was focused on evaluating the relationship between fracture-related dolomite and dolomite constrained by primary rock fabric in the 3 most prolific reservoir intervals in the Michigan Basin. The characterization of select dolomite reservoirs was the major focus of our efforts in Phases I and II of the project. Structural mapping and log analysis in the Dundee (Devonian) and Trenton/Black River (Ordovician) suggest a close spatial relationship among gross dolomite distribution and regional-scale, wrench fault-related NW-SE and NE-SW structural trends. A high temperature origin for much of the dolomite in these 2 studied intervals (based upon fluid inclusion homogenization temperatures and stable isotopic analyses,) coupled with persistent association of this dolomite in reservoirs coincident with wrench fault-related features, is strong evidence for these reservoirs being influenced by hydrothermal dolomitization. In the Niagaran (Silurian), there is a general trend of increasing dolomitization shelfward, with limestone predominant in more basinward positions. A major finding is that facies types, when analyzed at a detailed level, are directly related to reservoir porosity and permeability in these dolomites which increases the predictability of reservoir quality in these units. This pattern is consistent with our original hypothesis of primary facies control on dolomitization and resulting reservoir quality at some level. The identification of distinct and predictable vertical stacking patterns within a hierarchical sequence and cycle framework provides a high degree of confidence at this point that the results should be exportable throughout the basin. Much of the data synthesis and modeling for the project was scheduled to be part of Year 3/Phase III, but the discontinuation of funding after Year 2 precluded those efforts

Interactions of the Calcite {10.4} Surface with Organic Compounds: Structure and Behaviour at Mineral – Organic Interfaces

DEFF Research Database (Denmark)

Hakim, S. S.; Olsson, M. H. M.; Sørensen, H. O.

2017-01-01

The structure and the strength of organic compound adsorption on mineral surfaces are of interest for a number of industrial and environmental applications, oil recovery, CO2 storage and contamination remediation. Biomineralised calcite plays an essential role in the function of many organisms...... that control crystal growth with organic macromolecules. Carbonate rocks, composed almost exclusively of calcite, host drinking water aquifers and oil reservoirs. In this study, we examined the ordering behaviour of several organic compounds and the thickness of the adsorbed layers formed on calcite {10...... monolayers. The results of this work indicate that adhered organic compounds from the surrounding environment can affect the surface behaviour, depending on properties of the organic compound....

Hydrogeochemical modelling of fluid–rock interactions triggered by seawater injection into oil reservoirs: Case study Miller field (UK North Sea)

International Nuclear Information System (INIS)

Fu, Yunjiao; Berk, Wolfgang van; Schulz, Hans-Martin

2012-01-01

A hydrogeochemical model is presented and applied to quantitatively elucidate interdependent reactions among minerals and formation water–seawater mixtures at elevated levels of CO 2 partial pressure. These hydrogeochemical reactions (including scale formation) occur within reservoir aquifers and wells and are driven by seawater injection. The model relies on chemical equilibrium thermodynamics and reproduces the compositional development of the produced water (formation water–seawater mixtures) of the Miller field, UK North Sea. This composition of the produced water deviates from its calculated composition, which could result solely from mixing of both the end members (formation water and seawater). This indicates the effect of hydrogeochemical reactions leading to the formation and/or the dissolution of mineral phases. A fairly good match between the modelled and measured chemical composition of produced water indicates that hydrogeochemical interactions achieve near-equilibrium conditions within the residence time of formation water–seawater mixtures at reservoir conditions. Hence the model enables identification of minerals (including scale minerals), to quantitatively reproduce and to predict their dissolution and/or formation. The modelling results indicate that admixing of seawater into formation water triggers the precipitation of Sr–Barite solid solution, CaSO 4 phases and dolomite. In contrast, calcite and microcrystalline quartz are dissolved along the seawater flow path from the injection well towards the production well. Depending on the fraction of seawater admixed, interdependent reactions induce profound modifications to the aquifer mineral phase assemblage. At low levels of seawater admixture, Ba–Sr sulfate solid solution is precipitated and coupled to concurrent dissolution of calcite and microcrystalline quartz. Massive dissolution of calcite and the formation of CaSO 4 phases and dolomite are triggered by intense seawater admixture

Adsorption of a novel reagent scheme on scheelite and calcite causing an effective flotation separation.

Science.gov (United States)

Gao, Yuesheng; Gao, Zhiyong; Sun, Wei; Yin, Zhigang; Wang, Jianjun; Hu, Yuehua

2018-02-15

The efficient separation of scheelite from calcium-bearing minerals, especially calcite, remains a challenge in practice. In this work, a novel reagent scheme incorporating a depressant of sodium hexametaphosphate (SHMP) and a collector mixture of octyl hydroxamic acid (HXMA-8) and sodium oleate (NaOl) was employed in both single and mixed binary mineral flotation, and it proved to be highly effective for the separation. Furthermore, the role of the pH value in the separation was evaluated. Additionally, the mechanism of the selective separation was investigated systemically via zeta potential measurements, fourier transform infrared (FTIR) spectroscopy analysis, X-ray photoelectron (XPS) spectroscopy analysis and crystal chemistry calculations. It turns out that the selective chemisorption of SHMP on calcite (in the form of complexation between H 2 PO 4 - /HPO 4 2- and Ca 2+ ) over scheelite is ascribed to the stronger reactivity and higher density of Ca ions on the commonly exposed surfaces of calcite minerals. The intense adsorption of HXMA-8 on scheelite over calcite due to the match of the OO distances in WO 4 2- of scheelite and CONHOH of HXMA-8 holds the key to the successful separation. We were also interested in warranting the previous claim that NaOl is readily adsorbed on both minerals via chemisorption. Our results provided valuable insights into the application of mixed collectors and an effective depressant for flotation separation. Copyright © 2017 Elsevier Inc. All rights reserved.

Optimal processing conditions for a dolomite cracker for cracking of tar from gasification of biomass fuels. Optimale procesbetingelser for en dolomitkrakker til krakning af tjaere fra forgasning af biobraendsler

Energy Technology Data Exchange (ETDEWEB)

Fjellerup, J.

1989-08-15

Gasification of fuels derived from biomass is of interest in connection with combined cycle systems. During gasification tar compounds can be produced, and these can block further stages of the process. As gas turbines are very sensitive to tar compounds it is necessary to remove the tar completely from the gas. The most effective method appears to be catalytic cracking and it is suggested that dolomite is an effective and cheap catalysator. Based on a survey of relevant literature, the aim was to discover optimal conditions for the process of dolomite cracking. It is concluded that it is important to decarbonate the dolomite before use, that dolomite is not suitable for use in fluidized beds as it can become eroded and is subsequently very quickly blown out, and that it is important to hold the temperature at a level of ca. 800 deg. C. Conditions for fixed bed cracking both with and without steam are also desderibed. (AB) 15 refs.

Stability of Basalt plus Anhydrite plus Calcite at HP-HT: Implications for Venus, the Earth and Mars

Science.gov (United States)

Martin, A. M.; Righter, K.; Treiman, A. H.

2010-01-01

"Canali" observed at Venus surface by Magellan are evidence for very long melt flows, but their composition and origin remain uncertain. The hypothesis of water-rich flow is not reasonable regarding the temperature at Venus surface. The length of these channels could not be explained by a silicate melt composition but more likely, by a carbonate-sulfate melt which has a much lower viscosity (Kargel et al 1994). One hypothesis is that calcite CaCO3 and anhydrite CaSO4 which are alteration products of basalts melted during meteorite impacts. A famous example recorded on the Earth (Chicxulub) produced melt and gas rich in carbon and sulfur. Calcite and sulfate evaporites are also present on Mars surface, associated with basalts. An impact on these materials might release C- and S-rich melt or fluid. Another type of planetary phenomenon (affecting only the Earth) might provoke a high pressure destabilization of basalt+anhydrite+calcite. Very high contents of C and S are measured in some Earth s magmas, either dissolved or in the form of crystals (Luhr 2008). As shown by the high H content and high fO2 of primary igneous anhydrite-bearing lavas, the high S content in their source may be explained by subduction of an anhydrite-bearing oceanic crust, either directly (by melting followed by eruption) or indirectly (by release of S-rich melt or fluid that metasomatize the mantle) . Calcite is a major product of oceanic sedimentation and alteration of the crust. Therefore, sulfate- and calcite-rich material may be subducted to high pressures and high temperatures (HP-HT) and release S- and C-rich melts or fluids which could influence the composition of subduction zone lavas or gases. Both phenomena - meteorite impact and subduction - imply HP-HT conditions - although the P-T-time paths are different. Some HP experimental/theoretical studies have been performed on basalt/eclogite, calcite and anhydrite separately or on a combination of two. In this study we performed piston

Effects of limestone petrography and calcite microstructure on OPC clinker raw meals burnability

Science.gov (United States)

Galimberti, Matteo; Marinoni, Nicoletta; Della Porta, Giovanna; Marchi, Maurizio; Dapiaggi, Monica

2017-10-01

Limestone represents the main raw material for ordinary Portland cement clinker production. In this study eight natural limestones from different geological environments were chosen to prepare raw meals for clinker manufacturing, aiming to define a parameter controlling the burnability. First, limestones were characterized by X-Ray Fluorescence, X-Ray Powder Diffraction and Optical Microscopy to assess their suitability for clinker production and their petrographic features. The average domains size and the microstrain of calcite were also determined by X-Ray Powder Diffraction line profile analysis. Then, each limestone was admixed with clay minerals to achieve the adequate chemical composition for clinker production. Raw meals were thermally threated at seven different temperatures, from 1000 to 1450 °C, to evaluate their behaviour on heating by ex situ X-Ray Powder Diffraction and to observe the final clinker morphology by Scanning Electron Microscopy. Results indicate the calcite microstrain is a reliable parameter to predict the burnability of the raw meals, in terms of calcium silicates growth and lime consumption. In particular, mixtures prepared starting from high-strained calcite exhibit a better burnability. Later, when the melt appears this correlation vanishes; however differences in the early burnability still reflect on the final clinker composition and texture.

Calcite/opal deposits at Yucca Mountain, Nevada: Pedogenic or hypogene?

International Nuclear Information System (INIS)

Hill, C.A.; Schluter, C.M.; Harmon, R.S.

1994-01-01

This study is part of the research program of the Yucca Mountain Project intended to provide the State of Nevada with a detailed assessment of the geology and geochemistry of Yucca Mountain and adjacent regions. The purpose of this paper is to consider all of the geological and geochemical data available for the calcite/opal deposits at Yucca Mountain and to ascertain whether this data favors a pedogenic or hyogene origin for these deposits. Far from being of esoteric concern, this subject is of paramount importance to the debate which rages around the suitability of Yucca Mountain as a high-level radioactive waste repository site. It is also the purpose of this paper to serve as a foundation for a lengthy feature article to be submitted for publication in 1994. In addition, a stand has been taken by the National Research Council of the National Academy of Sciences against the upwelling-water model (a vote of 17 to 0 against), and this same panel report has concluded that open-quotes there is no compelling evidence for the repetitive flooding of the environment by expulsion of groundwaterclose quotes and that open-quotes instead, the evidence strongly supports the idea that the near-surface mineral deposits resulted from percolating rainwater, which carried soil minerals down into rock fracturesclose quotes. Based on such information the Department of Energy has stated that it open-quotes finds no basis to continue to study the origin of these specific depositsclose quotes. This study, based upon many different independent lines of evidence, reaches the opposite conclusion and instead favors a hypogene spring-travertine origin for the controversial calcite/opal deposits at Yucca Mountain. This study recognizes a pedogenic carbonate component at Yucca Mountain, but argues that this component is distinct from, and sometimes intermixed with, the calcite/opal deposits

Calcite production by coccolithophores in the south east Pacific Ocean

Directory of Open Access Journals (Sweden)

L. Beaufort

2008-08-01

Full Text Available BIOSOPE cruise covered an oceanographic transect through the centre of the South Pacific Gyre (SPG from the Marquesas archipelago to the Peru-Chile upwelling (PCU. Water samples from 6 depths in the euphotic zone were collected at 20 stations. The concentrations of suspended calcite particles, coccolithophores cells and detached coccoliths were estimated together with size and weight using an automatic polarizing microscope, a digital camera, and a collection of softwares performing morphometry and pattern recognition. Some of these softwares are new and described here for the first time. The coccolithophores standing stocks were usually low and reached maxima west of the PCU. The coccoliths of Emiliania huxleyi, Gephyrocapsa spp. and Crenalithus spp. (Order Isochrysidales represented more than 30% of all the suspended calcite particles detected in the size range 0.1–46 μm (22% of PIC in term of calcite weight. These species grew preferentially in the Chlorophyll maximum zone. In the SPG their maximum cell concentrations were recorded between depth of 150 and 200 m, which is unusually deep for these taxa. The weight of coccoliths and coccospheres were correlated to their size. Large and heavy coccoliths and coccospheres were found in regions with relatively high fertility in the Marquises Island and in the PCU. Small and light coccoliths and coccospheres were found west of the PCU. This distribution is strongly related to ocean chemistry in particular to alkalinity and to carbonate ions concentration. The biotic (coccolithophores production influence on calcification is mainly driven at the local scale (depth whereas the abiotic (carbonate chemistry plays its most important role at the regional (horizontal level. Here 94% of the variability of coccolith and coccosphere weight can be explained by a change in 7 environmental variables.

Improvement Of The U-Th Method For Dating Of Impure Calcite Having A Large Amount Of Clay And Very Low Uranium Content

Directory of Open Access Journals (Sweden)

Samer Farkh

2015-01-01

Full Text Available Abstract The U-Th method also called series method of uranium is improved by a new experimental protocol and successfully applied to the impure calcite with uranium concentration 005 dpmg which was previously difficult to be dated accurately. Our experiments performed on 15 calcite samples taken from France and Morocco have highlighted the importance of this methodological improvement by enabling i the elimination of 100 of clay residues ii the reduction of calcite quantity necessary to the chemical manipulation from 20g to 5g iii the analysis of calcite samples poor in uranium and on the other hand rich with clay and iiii the reduction of the lower limit of the U-Th method from 10 Kyrs to 6 Kyrs. The optimization of U-Th method in this work provided a better dating of the accurate age of calcite. Thus this technique is important for the chemical analysis of stalagmite floors of different caves in the region of the Near East.

Nano-structured calcite produced by micro-organisms in ancient and modern loess in Chinese Loess Plateau

Science.gov (United States)

Xu, H.; Chen, T.; Lu, H.; Wang, X.

2005-12-01

The results from transmission electron microscopy (TEM) and field emission gun scanning microscopy (FEG-SEM) investigation show that there are calcite nano-fibers (CNFs) formed during pedogenic process. The CNFs are widely distributed in the loess and red clay samples of Caoxian, Luochuan, Lingtai, Lantian, and Xifeng profiles as well as the samples of modern surface loess soils in Chinese Loess Plateau. Diameters of all the NFCs are about 40 nm, the length of the CNFs ranges from tens nanometer to several micrometers. Elongation direction of NFCs is unusual near parallel (105)* or (115)*. Crystals of NFCs arrange as bird net like and lattice-like frameworks. X-ray EDS spectra show the weak peaks of magnesium, phosphorous, and sulfur. Our investigation indicates that CNFs are in pore space of loess and paleosol and made up most of carbonate except for caliche nodular layers. Concentration of NFCs in the loess layers are significantly higher than those of paleosol layers because of leaching of carbonate in the paleosol forming environment (warn and wet paleoclimate). The "nanobacteria-like CNFs are well crystalline calcite single crystals with smoothes surfaces. The morphologies of CNFs are very unusual and different from the calcite single crystals observed in most geological environments. The CNFs are directly related to microbial activities in both ancient and modern loess. It is proposed that the intervention of organic compounds derived from microbial activities control the formation of the calcite nano-fibers. Both morphology and bulk composition of CNFs indicate that the formation of the CNFs involves bio-organics derived from microorganisms in loess deposit environment. Formation conditions of the calcite nano-fibers may information about paleoclimate, paleo-environment and paleoecology. So, the discovery of CNFs in loess-paloesol sequences can provide a new route for reconstruct paleoclimate by oxygen and carbon isotope from the CNFs.

Acidizing of Zechstein Main Dolomite in the Polish lowlands

Energy Technology Data Exchange (ETDEWEB)

Bierdzychi, W

1966-07-01

The first acidizing of Zechstein Dolomite in the Polish Lowlands was carried out in 1961. In the initial stage, a tendency existed toward multistage acidizing, and preheated acidizing fluid was used. In a preliminary operation, an acid having the concentration 12-36% was used for washing out the borehole. No additives were utilized except formalin for corrosion inhibition. In order to increase the absorption capacity, hydraulic perforations were used. The composition of acidizing fluid was determined in a preliminary study for any individual reservoir. From laboratory study, it was concluded also that the required time of 3-4 hr was sufficient for the exhaustion of acid. The pre-heating of the acid at the bottom of the hole by exothermic reaction with metallic magnesium was abandoned in the later stage of operations.

Carbonate microbialites and hardgrounds from Manito Lake, an alkaline, hypersaline lake in the northern Great Plains of Canada

Science.gov (United States)

Last, Fawn M.; Last, William M.; Halden, Norman M.

2010-03-01

Manito Lake is a large, perennial, Na-SO 4 dominated saline to hypersaline lake located in the northern Great Plains of western Canada. Significant water level decrease over the past several decades has led to reduction in volume and surface area, as well as an increase in salinity. The salinity has increased from 10 ppt to about 50 ppt TDS. This decrease in water level has exposed large areas of nearshore microbialites. These organogenic structures range in size from several cm to over a meter and often form large bioherms several meters high. They have various external morphologies, vary in mineralogical composition, and show a variety of internal fabrics from finely laminated to massive. In addition to microbiolities and bioherms, the littoral zone of Manito Lake contains a variety of carbonate hardgrounds, pavements, and cemented clastic sediments. Dolomite and aragonite are the most common minerals found in these shoreline structures, however, calcite after ikaite, monohydrocalcite, magnesian calcite, and hydromagnesite are also present. The dolomite is nonstoichiometric and calcium-rich; the magnesian calcite has about 17 mol% MgCO 3. AMS radiocarbon dating of paired organic matter and endogenic carbonate material confirms little or no reservoir affect. Although there is abundant evidence for modern carbonate mineral precipitation and microbialite formation, most of the larger microbialites formed between about 2300 and 1000 cal BP, whereas the hardgrounds, cements, and laminated crusts formed about 1000-500 cal BP.

Ethanol adsorption on the {10(1)over-bar4} calcite surface

DEFF Research Database (Denmark)

Sand, Karina Krarup; Stipp, Susan Louise Svane; Hassenkam, Tue

2008-01-01

Preliminary atomic force microscopy investigations of the {10 (1) over bar4} calcite Surface cleaved in ethanol indicate a different surface behaviour than that of the {10 (1) over bar4} surface cleaved in air. The results are consistent with recent theoretical studies and suggest strong ordering...

Sturgeon and paddlefish (Acipenseridae) sagittal otoliths are composed of the calcium carbonate polymorphs vaterite and calcite.

Science.gov (United States)

Pracheil, B M; Chakoumakos, B C; Feygenson, M; Whitledge, G W; Koenigs, R P; Bruch, R M

2017-02-01

This study sought to resolve whether sturgeon (Acipenseridae) sagittae (otoliths) contain a non-vaterite fraction and to quantify how large a non-vaterite fraction is using neutron diffraction analysis. This study found that all otoliths examined had a calcite fraction that ranged from 18 ± 6 to 36 ± 3% by mass. This calcite fraction is most probably due to biological variation during otolith formation rather than an artefact of polymorph transformation during preparation. © 2016 The Fisheries Society of the British Isles.

Origin of ultramafic-hosted magnesite on Margarita Island, Venezuela

Science.gov (United States)

Abu-Jaber, N. S.; Kimberley, M. M.

1992-06-01

Ultramafic-hosted deposits of magnesite (MgCO3) have been studied on Margarita Island, Venezuela, to elucidate the source of carbon and conditions of formation for this type of ore. Petrographic, mineralogic, and δ18O data indicate that magnesite precipitated on Margarita in near-surface environments at low P and T. δ13C ranges from -9 to -16‰ PDB within the magnesite and -8 to -10‰ PDB within some calcite and dolomite elsewhere on the island. The isotopically light dolomite fills karst and the calcite occurs as stock-work veins which resemble the magnesite deposits. These carbon isotopic ratios are consistent with a deep-seated source rather than an overlying source from a zone of surficial weathering. However, there is not much enrichment of precious metals and no enrichment of heavy rare-earth elements, as would be expected if the carbon had migrated upward as aqueous carbonate ions. The carbon probably has risen as a gaseous mixture of CO2 and CH4 which partially dissolved in near-surface water before leaching cations and precipitating as magnesite and other carbonates. The process probably is ongoing, given regional exhalation of carbonaceous gases.

Interaction of ethanol and water with the {1014} surface of calcite

DEFF Research Database (Denmark)

Cooke, David; Gray, R J; Sand, K K

2010-01-01

Molecular dynamics simulations have been used to model the interaction between ethanol, water, and the {1014} surface of calcite. Our results demonstrate that a single ethanol molecule is able to form two interactions with the mineral surface (both Ca-O and O-H), resulting in a highly ordered, st...

Thermoluminescent of induced calcite by gamma and ultraviolet radiation

International Nuclear Information System (INIS)

Lima, J.F. de.

1987-01-01

Samples of brazilian calcite, exposed to gamma radiation in laboratory and heated at constant rate of 2.7 0 C/s, showed three glow peaks at 150, 250 and 350 0 C in their thermoluminescent emission curves. The analysis of these peaks, using different models, indicated that they follow a second order kinetics; it has been obtained, for the activation energy, 1.3, 1.5 and 1.7 eV, and, for the pre-exponential factors, 8.1 x 10 14 , 6.8 x10 13 and 2.4 x 10 12 s -1 . Although the total thermoluminescent emission has stayed constant, the relative height of glow peaks has changed with the temperature of annealing in the range of 400 to 700 0 C. Exposed samples were also illuminated with ultraviolet light and the resultant curves showed partial or total bleaching or some glow peaks and the growth of peaks at lower temperatures. Samples of virgin calcite, submited to increasing exposures of gamma rays, showed a corresponding enhancement of the optical absorption bands in the range of 25000 to 47000 cm -1 A subsequent illumination of these samples with ultraviolet light produced a decrease of the optical absorption bands at the same range. (author) [pt

Methodology for the study of the dolomite porosity in essay of interrupted sulfation

OpenAIRE

Ávila, Ivonete; Crnkovic, Paula M.; Milioli, Fernando E.

2010-01-01

The aim of this work is to propose a methodology to evaluate the evolution of the pore blockage of limestone during the sulfation reaction. The experiments were performed for a national limestone (dolomite) with average particle size of 545 μm in interrupted sulfation tests were conducted at seven different times and at three different temperatures of the process. The empirical data were obtained from porosimetry tests to establish BET surface area, volume and average size of pore and di...

Use of dolomite phosphate rock (DPR) fertilizers to reduce phosphorus leaching from sandy soil

International Nuclear Information System (INIS)

Chen, G.C.; He, Z.L.; Stoffella, P.J.; Yang, X.E.; Yu, S.; Calvert, D.

2006-01-01

There is increasing concern over P leaching from sandy soils applied with water-soluble P fertilizers. Laboratory column leaching experiments were conducted to evaluate P leaching from a typical acidic sandy soil in Florida amended with DPR fertilizers developed from dolomite phosphate rock (DPR) and N-Viro soil. Ten leaching events were carried out at an interval of 7 days, with a total leaching volume of 1183 mm equivalent to the mean annual rainfall of this region during the period of 2001-2003. Leachates were collected and analyzed for total P and inorganic P. Phosphorus in the leachate was dominantly reactive, accounting for 67.7-99.9% of total P leached. Phosphorus leaching loss mainly occurred in the first three leaching events, accounting for 62.0-98.8% of the total P leached over the whole period. The percentage of P leached (in the total P added) from the soil amended with water-soluble P fertilizer was higher than those receiving the DPR fertilizers. The former was up to 96.6%, whereas the latter ranged from 0.3% to 3.8%. These results indicate that the use of N-Viro-based DPR fertilizers can reduce P leaching from sandy soils. - Fertilizers developed from dolomite phosphate rock (DPR) reduce phosphorus leaching from sandy soil

Growth kinetics of racemic heptahelicene-2-carboxylic acid nanowires on calcite (104)

Czech Academy of Sciences Publication Activity Database

Einax, M.; Richter, T.; Nimmrich, M.; Rahe, P.; Stará, Irena G.; Starý, Ivo; Kühnle, A.; Maass, P.

2016-01-01

Roč. 145, č. 13 (2016), č. článku 134702. ISSN 0021-9606 Institutional support: RVO:61388963 Keywords : heptahelicene-2-carboxylic acid nanowires * nc-AFM * calcite * growth kinetics Subject RIV: CC - Organic Chemistry Impact factor: 2.965, year: 2016

Temporal occurrence and activity of landslides in the area of Cortina d'Ampezzo (Dolomites, Italy)

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Panizza, Mario; Pasuto, Alessandro; Silvano, Sandro; Soldati, Mauro

1996-04-01

This article shows the results of research on landslides carried out in the area of Cortina d'Ampezzo (Dolomites, Italy) within the framework of the EPOCH Project of the European Community. The investigated area, where tourism activities and infrastructures are highly developed, has been affected by several landslides since the retreat of the Würnian glaciers and is at present still affected by active slides and flows which endanger some villages. After a geological and geomorphological description, the distribution in space and time of landslides which occurred in the surroundings of Cortina d'Ampezzo is presented. The type, activity, frequency and, when possible, the age of mass movements have been outlined. Furthermore, special attention is focused on the landslides active at present which are reactivations of ancient movements. The results from the monitoring systems, which were installed in order to survey kinematic and hydrogeologic parameters and define the movement rate, are shown. The research enables the reconstruction of the post-Würmian geomorphological evolution of a site in the Dolomites that appears to be very peculiar both on account of the wide distribution of landslides and the intense human activity.

Intrinsic versus extrinsic controls on the development of calcite dendrite bushes, Shuzhishi Spring, Rehai geothermal area, Tengchong, Yunnan Province, China

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Jones, Brian; Peng, Xiaotong

2012-04-01

In the Rehai geothermal area, located near Tengchong, there is an old succession of crystalline calcite that formed from a spring that is no longer active. The thin-bedded succession, exposed on the south bank of Zaotang River, is formed of three-dimensional dendrite bushes that are up to 6 cm high and 3 cm in diameter with multiple levels of branching. Bedding is defined by color, which ranges from white to gray to almost black and locally accentuated by differential weathering that highlights the branching motif of the dendrites. The succession developed through repeated tripartite growth cycles that involved: Phase I that was characterized by rapid vertical growth of the dendrite bushes with ever-increasing branching; Phase II that developed once growth of the dendrites had almost or totally ceased, and involved an initial phase of etching that was followed by the precipitation of various secondary minerals (sheet calcite, trigonal calcite crystals, hexagonal calcite crystals, hexagonal plates formed of Ca and P, Mn precipitates, Si-Mg reticulate coatings, opal-CT lepispheres) on the branches of the calcite dendrites, and Phase III that involved deposition of detrital quartz, feldspar, clay, and calcite on top of the dendrite bushes. The tripartite growth cycle is attributed primarily to aperiodic cycles in the CO2 content of the spring water that was controlled by subsurface igneous activity rather than climatic controls. High CO2 coupled with rapid CO2 degassing triggered growth of the dendrite bushes. As CO2 levels waned, saturation levels in the spring water decreased and calcite dendrite growth ceased and precipitation of the secondary minerals took place, possibly in the microcosms of microbial mats. Deposition of the detrital sediment was probably related to surface runoff that was triggered by periods of high rainfall. Critically, this study shows that intrinsic factors rather than extrinsic factors (e.g., climate) were the prime control on the

Physicochemical Processes and the Evolution of Strength in Calcite Fault Gouge at Room Temperature

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Carpenter, B. M.; Viti, C.; Collettini, C.

2015-12-01

The presence of calcite in and near faults, as the dominant material, cement, or vein fill, indicates that the mechanical behavior of carbonate-dominated material likely plays an important role in shallow- and mid-crustal faulting. Furthermore, a variety of physical and chemical processes control the evolution of strength and style of slip along seismogenic faults and thus play a critical role in the seismic cycle. Determining the role and contributions of these types of mechanisms is essential to furthering our understanding of the processes and timescales that lead to the strengthening of faults during interseismic periods and their behavior during the earthquake nucleation process. To further our understanding of these processes, we performed laboratory-shearing experiments on calcite gouge at normal stresses from 1 to 100 MPa, under conditions of saturation and at room temperature. We performed velocity stepping (0.1-1000μm/s) and slide-hold-slide (1-3000s) tests, to measure the velocity dependence of friction and the amount of frictional strengthening respectively, under saturated conditions with pore fluid that was in equilibrium with CaCO3. At 5 MPa normal stress, we also varied the environmental conditions by performing experiments under conditions of 5% RH and 50 % RH, and saturation with: silicone oil, demineralized water, and the equilibrated solution combined with 0.5M NaCl. Finally, we collected post experimental samples for microscopic analysis. Our combined analyses of rate-dependence, strengthening behavior, and microstructures show that calcite fault gouge transitions from brittle to semi-brittle behavior at high normal stress and low sliding velocities. Furthermore, our results also highlight how changes in pore water chemistry can have significant influence on the mechanical behavior of calcite gouge in both the laboratory and in natural faults. Our observations have important implications for earthquake nucleation and propagation on faults in

Scrap tire pyrolysis using a new type two-stage pyrolyzer: Effects of dolomite and olivine on producing a low-sulfur pyrolysis oil

International Nuclear Information System (INIS)

Choi, Gyung-Goo; Oh, Seung-Jin; Kim, Joo-Sik

2016-01-01

Scrap tire pyrolysis was performed using a two-stage pyrolyzer consisting of an auger reactor and a fluidized bed reactor to produce a low-sulfur pyrolysis oil. In the experiments, the effect of the residence time of the feed material in the auger reactor was investigated at ∼300 (auger reactor) and 500 °C (fluidized bed reactor). In addition, natural dolomite and olivine and calcined dolomite and olivine were used as the fluidized bed materials to examine their effects on reducing the sulfur content of pyrolysis oil. In the experiments, the yields of the oil from the auger reactor were 1.4–3.7 wt%, and it was enriched with DL-limonene whose content in the oil was 40–50 wt%. The yields of the oil from the fluidized bed reactor were 42–46 wt%. The optimum residence time of the feed material in the auger reactor turned out to be 3.5 min. Calcined dolomite and olivine significantly decreased the sulfur content of pyrolysis oil. Metal oxides of the additives appeared to react with H_2S to form metal sulfides. The sulfur content of pyrolysis oil obtained with calcined olivine was 0.45 wt%. - Highlights: • Scrap tires were successfully pyrolyzed in a new type two-stage pyrolyzer. • The two-stage pyrolyzer is composed of an auger and fluidized bed reactors. • Calcination of olivine and dolomite led to a strong decrease in sulfur. • The lowest sulfur content of pyrolysis oil was 0.45 wt%. • Pyrolysis oil yields from the fluidized bed reactor were 43–46 wt%.

Dolomitic lime amendment affects pine bark substrate pH, nutrient availability, and plant growth: A review

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Dolomitic lime (DL) is one of the most commonly used fertilizer amendments in nursery container substrates. It is used to adjust pH of pine bark substrates from their native pH, 4.1 to 5.1, up to about pH 6. Additions of DL have been shown to be beneficial, inconsequential, or detrimental dependin...

Application of kinetic models to the design of a calcite permeable reactive barrier (PRB) for fluoride remediation.

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Cai, Qianqian; Turner, Brett D; Sheng, Daichao; Sloan, Scott

2018-03-01

The kinetics of fluoride sorption by calcite in the presence of metal ions (Co, Mn, Cd and Ba) have been investigated and modelled using the intra-particle diffusion (IPD), pseudo-second order (PSO), and the Hill 4 and Hill 5 kinetic models. Model comparison using the Akaike Information Criterion (AIC), the Schwarz Bayseian Information Criterion (BIC) and the Bayes Factor allows direct comparison of model results irrespective of the number of model parameters. Information Criterion results indicate "very strong" evidence that the Hill 5 model was the best fitting model for all observed data due to its ability to fit sigmoidal data, with confidence contour analysis showing the model parameters were well constrained by the data. Kinetic results were used to determine the thickness of a calcite permeable reactive barrier required to achieve up to 99.9% fluoride removal at a groundwater flow of 0.1 m.day -1 . Fluoride removal half-life (t 0.5 ) values were found to increase in the order Ba ≈ stonedust (a 99% pure natural calcite) barrier width of 0.97 ± 0.02 m was found to be required for the fluoride/calcite (stonedust) only system when using no factor of safety, whilst in the presence of Mn and Co, the width increased to 2.76 ± 0.28 and 19.83 ± 0.37 m respectively. In comparison, the PSO model predicted a required barrier thickness of ∼46.0, 62.6 & 50.3 m respectively for the fluoride/calcite, Mn and Co systems under the same conditions. Crown Copyright © 2017. Published by Elsevier Ltd. All rights reserved.

Calcite twinning strain variations across the Proterozoic Grenville orogen and Keweenaw-Kapuskasing inverted foreland, USA and Canada

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John P. Craddock

2017-11-01

Full Text Available We report the calcite twinning strain results of a traverse across the Grenville orogen from Parry Sound, Ontario (NW to Ft. Ann, New York (SE, including the younger, adjacent Ordovician Taconic allochthon. Fifty four carbonates (marbles, calcite veins, Ordovician limestone were collected resulting in 68 strain analyses on mechanically twinned calcite (n = 2337 grains across the Central Gneiss Belt (CGB; 3 samples, the Central Metasedimentary Belt (CMB; 27 samples, the Central Granulite Terrane (CGT; Adirondack's; 13 samples and the Ottawan Orogenic Lid (OOL; 11 samples. Twinning strains in the greenschist-grade OOL marbles preserve N–S shortening and U-Pb titanite ages (∼1150 Ma; n = 4 document these marbles formed during the Shawinigan (1190–1140 Ma part of the Grenville orogen. From northwest to southeast, the Ottawan (1095–1020 Ma twinning strain is dominantly a layer-parallel shortening fabric oriented N–S (Parry Sound, then becomes parallel to the Grenville thrust direction (NW–SE across the CMB to the Adirondack Highlands where the sub-horizontal shortening strain becomes margin-parallel (SW–NE. Within the regional sample suite there are two areas studied in detail, the Bancroft shear zone (n = 11 and a roadcut on the southeast side of the Adirondack Mountains (Ft. Ann, NY; n = 8. Marbles from the Bancroft shear zone contain calcite grains with 2 sets of twin lamellae (e1 and e2. The better-developed e1 sets (n = 406 record a horizontal fabric oriented NW–SE whereas the younger e2 lamellae (n = 146 preserve a margin-parallel (SW–NE horizontal fabric. Both the e1 and e2 strains record an overprint vertical shortening strain (NEV, perhaps related to extensional orogenic collapse. We also report an Ottawan orogen-aged granoblastic mylonite (1093 Ma, U-Pb zircon; 1102 Ma Ar-Ar biotite in the Keweenaw thrust hanging wall 500 km inboard of the Grenville front and interpret the relations of Grenville

Mechanical changes caused by CO2-driven cement dissolution in the Morrow B Sandstone at reservoir conditions: Experimental observations

Science.gov (United States)

Wu, Z.; Luhmann, A. J.; Rinehart, A. J.; Mozley, P.; Dewers, T. A.

2017-12-01

Carbon Capture, Utilization and Storage (CCUS) in transmissive reservoirs is a proposed mechanism in reducing CO2 emissions. Injection of CO2 perturbs reservoir chemistry, and can modify porosity and permeability and alter mineralogy. However, little work has been done on the coupling of rock alteration by CO2 injection and the mechanical integrity of the reservoir. In this study, we perform flow-through experiments on calcite- and dolomite-cemented Pennsylvanian Morrow B Sandstone (West Texas, USA) cores. We hypothesize that poikilotopic calcite cement has a larger impact on chemo-mechanical alteration than disseminated dolomite cement given similar CO2 exposure. With one control brine flow-through experiment and two CO2-plus-brine flow-through experiments for each cement composition, flow rates of 0.1 and 0.01 ml/min were applied under 4200 psi pore fluid pressure and 5000 psi confining pressure at 71 °C. Fluid chemistry and permeability data enable monitoring of mineral dissolution. Ultrasonic velocities were measured pre-test using 1.2 MHz source-receiver pairs at 0.5 MPa axial load and show calcite-cemented samples with higher dynamic elastic moduli than dolomite-cemented samples. Velocities measured post-experiment will identify changes from fluid-rock interaction. We plan to conduct cylinder-splitting destructive mechanical test (Brazil test) to measure the pristine and altered tensile strength of different cemented sandstones. The experiments will identify extents to which cement composition and texture control chemo-mechanical degradation of CCUS reservoirs. Funding for this project is provided by the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL) through the Southwest Regional Partnership on Carbon Sequestration (SWP) under Award No. DE-FC26-05NT42591. Sandia National Laboratories is a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia LLC, a wholly owned subsidiary of

Review: geological and experimental evidence for secular variation in seawater Mg/Ca (calcite-aragonite seas and its effects on marine biological calcification

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J. B. Ries

2010-09-01

Full Text Available Synchronized transitions in the polymorph mineralogy of the major reef-building and sediment-producing calcareous marine organisms and abiotic CaCO₃ precipitates (ooids, marine cements throughout Phanerozoic time are believed to have been caused by tectonically induced variations in the Mg/Ca ratio of seawater (molar Mg/Ca>2="aragonite seas", <2="calcite seas". Here, I assess the geological evidence in support of secular variation in seawater Mg/Ca and its effects on marine calcifiers, and review a series of recent experiments that investigate the effects of seawater Mg/Ca (1.0–5.2 on extant representatives of calcifying taxa that have experienced variations in this ionic ratio of seawater throughout the geologic past.

Secular variation in seawater Mg/Ca is supported by synchronized secular variations in (1 the ionic composition of fluid inclusions in primary marine halite, (2 the mineralogies of late stage marine evaporites, abiogenic carbonates, and reef- and sediment-forming marine calcifiers, (3 the Mg/Ca ratios of fossil echinoderms, molluscs, rugose corals, and abiogenic carbonates, (4 global rates of tectonism that drive the exchange of Mg²⁺ and Ca²⁺ along zones of ocean crust production, and (5 additional proxies of seawater Mg/Ca including Sr/Mg ratios of abiogenic carbonates, Sr/Ca ratios of biogenic carbonates, and Br concentrations in marine halite.

Laboratory experiments have revealed that aragonite-secreting bryopsidalean algae and scleractinian corals and calcite-secreting coccolithophores exhibit higher rates of calcification and growth in experimental seawaters formulated with seawater Mg/Ca ratios that favor their skeletal mineral. These results support the assertion that seawater Mg/Ca played an important role in determining which hypercalcifying marine organisms were the major reef-builders and sediment-producers throughout Earth history. The observation that primary

Effect of coccolith polysaccharides isolated from the coccolithophorid, Emiliania huxleyi, on calcite crystal formation in in vitro CaCO3 crystallization.

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Kayano, Keisuke; Saruwatari, Kazuko; Kogure, Toshihiro; Shiraiwa, Yoshihiro

2011-02-01

Marine coccolithophorids (Haptophyceae) produce calcified scales "coccoliths" which are composed of CaCO(3) and coccolith polysaccharides (CP) in the coccolith vesicles. CP was previously reported to be composed of uronic acids and sulfated residues, etc. attached to the polymannose main chain. Although anionic polymers are generally known to play key roles in biomineralization process, there is no experimental data how CP contributes to calcite crystal formation in the coccolithophorids. CP used was isolated from the most abundant coccolithophorid, Emiliania huxleyi. CaCO(3) crystallization experiment was performed on agar template layered onto a plastic plate that was dipped in the CaCO(3) crystallization solution. The typical rhombohedral calcite crystals were formed in the absence of CP. CaCO(3) crystals formed on the naked plastic plate were obviously changed to stick-like shapes when CP was present in the solution. EBSD analysis proved that the crystal is calcite of which c-axis was elongated. CP in the solution stimulated the formation of tabular crystals with flat edge in the agarose gel. SEM and FIB-TEM observations showed that the calcite crystals were formed in the gel. The formation of crystals without flat edge was stimulated when CP was preliminarily added in the gel. These observations suggest that CP has two functions: namely, one is to elongate the calcite crystal along c-axis and another is to induce tabular calcite crystal formation in the agarose gel. Thus, CP may function for the formation of highly elaborate species-specific structures of coccoliths in coccolithophorids.

Transformation of amorphous calcium carbonate to rod-like single crystal calcite via "copying" collagen template.

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Xue, Zhonghui; Hu, Binbin; Dai, Shuxi; Du, Zuliang

2015-10-01

Collagen Langmuir films were prepared by spreading the solution of collagen over deionized water, CaCl2 solution and Ca(HCO3)2 solution. Resultant collagen Langmuir monolayers were then compressed to a lateral pressure of 10 mN/m and held there for different duration, allowing the crystallization of CaCO3. The effect of crystallization time on the phase composition and microstructure of CaCO3 was investigated. It was found that amorphous calcium carbonate (ACC) was obtained at a crystallization time of 6 h. The amorphous CaCO3 was transformed to rod-like single crystal calcite crystals at an extended crystallization time of 12 h and 24 h, via "copying" the symmetry and dimensionalities of collagen fibers. Resultant calcite crystallites were well oriented along the longitudinal axis of collagen fibers. The ordered surface structure of collagen fibers and electrostatic interactions played key roles in tuning the oriented nucleation and growth of the calcite crystallites. The mineralized collagen possessing both desired mechanical properties of collagen fiber and good biocompatibility of calcium carbonate may be assembled into an ideal biomaterial for bone implants. Copyright © 2015. Published by Elsevier B.V.

Ab initio study of single-crystalline and polycrystalline elastic properties of Mg-substituted calcite crystals.

Science.gov (United States)

Zhu, L-F; Friák, M; Lymperakis, L; Titrian, H; Aydin, U; Janus, A M; Fabritius, H-O; Ziegler, A; Nikolov, S; Hemzalová, P; Raabe, D; Neugebauer, J

2013-04-01

We employ ab initio calculations and investigate the single-crystalline elastic properties of (Ca,Mg)CO3 crystals covering the whole range of concentrations from pure calcite CaCO3 to pure magnesite MgCO3. Studying different distributions of Ca and Mg atoms within 30-atom supercells, our theoretical results show that the energetically most favorable configurations are characterized by elastic constants that nearly monotonously increase with the Mg content. Based on the first principles-derived single-crystalline elastic anisotropy, the integral elastic response of (Ca,Mg)CO3 polycrystals is determined employing a mean-field self-consistent homogenization method. As in case of single-crystalline elastic properties, the computed polycrystalline elastic parameters sensitively depend on the chemical composition and show a significant stiffening impact of Mg atoms on calcite crystals in agreement with the experimental findings. Our analysis also shows that it is not advantageous to use a higher-scale two-phase mix of stoichiometric calcite and magnesite instead of substituting Ca atoms by Mg ones on the atomic scale. Such two-phase composites are not significantly thermodynamically favorable and do not provide any strong additional stiffening effect. Copyright © 2013 Elsevier Ltd. All rights reserved.

The effect of annealing atmosphere on the thermoluminescence of synthetic calcite

International Nuclear Information System (INIS)

Pagonis, Vasilis

1998-01-01

Samples of high purity calcite powder were annealed in air, nitrogen and carbon dioxide atmospheres in the temperature range 300-700 deg. C and in atmospheric pressure. The samples were subsequently irradiated and the effect of the annealing atmosphere and temperature on the thermoluminescence (TL) of the samples was studied. Our results show that both carbonate and oxygen ions play an important part in the TL of calcite annealed in this temperature range. The intensities of the TL signal in the nitrogen and carbon dioxide anneals rise continuously with the annealing temperature. For all annealing temperatures it was found that the carbon dioxide atmosphere caused an increase in the observed TL signal as compared with anneals in an inert nitrogen atmosphere, while the shape of the TL glow curves remained the same. This increase in the observed TL signal is explained via the surface adsorption of carbonate ions. The shape and location of the TL peaks suggest that samples annealed in air exhibit a different type of TL center than samples annealed in nitrogen and carbon dioxide atmospheres. A possible mechanism for the role of oxygen ions involves a surface adsorption process and a subsequent diffusion of oxygen ions in the bulk of the crystal. Annealing of the samples in air at temperatures T>600 deg. C causes a collapse of the TL signal, in agreement with previous studies of calcite powders. No such collapse of the TL signal is observed for the nitrogen and carbon dioxide anneals, suggesting that a different type of TL center and/or recombination center is involved in air anneals. Arrhenius plots for the air anneals yield an activation energy E=0.45±0.05 eV, while the carbon dioxide and nitrogen anneals yield a lower activation energy E=0.28±0.04 eV

Mineralogical, geochemical and hydrocarbon potential of subsurface Cretaceous shales, Northern Western Desert, Egypt

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D.A. Mousa

2014-03-01

Full Text Available Twenty four Cretaceous shale core samples of Gibb Afia-1, Betty-1, Salam-1X and Mersa Matruh-1 wells were mineralogically and geochemically studied using XRD, XRF and Rock Eval Pyrolysis. Kaolinite, smectite and illite are the main clay minerals in addition to rare chlorite, while the non-clay minerals include quartz, calcite, dolomite and rare siderite. The shales were derived through intensive chemical weathering of mafic basement and older sedimentary rocks. These sediments were deposited in a near-shore shallow marine environment with some terrestrial material input. The shales have poor to fair organic content. It is marginally to rarely mature.

Dolomitization of carbonated reservoirs of platforms. From geologic data to modeling. Example of the great Bahama bank; La dolomitisation des reservoirs carbonates de plate-forme. Des donnees geologiques a la modelisation. Exemple du Grand Banc des Bahamas

Energy Technology Data Exchange (ETDEWEB)

Caspard, E.

2002-09-01

Dolomitization has long been one of the most studied geological processes because of its economic interest (dolomitic rocks form a significant share of hydrocarbon reservoirs) as well as its academic interest, based on the fact that dolomite scarcely forms in current and recent marine environments whereas seawater is highly over-saturated; and that it is still not possible to synthesize it in laboratory under the same conditions. We used data collected by the University of Miami (Bahamas Drilling Project, ODP Leg 166) to understand the geological context of complete dolomitization of a Messinian 60 m thick reef unit. Classical methods of petrographic analysis of thin sections (optical microscopy, cathodoluminescence, scanning electron microscopy, in situ isotopic analyze using ionic microprobe) showed that the intensity of dolomitization is not controlled by the initial texture of the sediment, that the key parameter for dolomitization is the conservation of the initial mineralogy of magnesian bio-clasts, and that redox conditions, salinity and/or temperature of the precipitation fluid varied significantly during the process. Hydrodynamic modelling showed that during periods of high sea-level, Kohout thermal convection is a viable mechanism for driving marine fluids through the sediments. The key parameter for fluid circulations is the permeability anisotropy on the platform scale. Geochemical modelling showed that seawater is able to induce a complete dolomitization over durations of around one million years. Sensitivity tests showed that the critical parameter (as well as one of the less well-known) to describe diagenetic processes in carbonates is the water/rock reactions kinetics and in particular the precipitation kinetics of carbonate minerals. We finally propose that the dolomitization of the reef unit of the Unda well took place during the high sea-level period which extended over 1,1 My in the early Pliocene, according to the Kohout thermal convection

Carbonatitic liquids and COH fluids from epidote-dolomite eclogites at 3.7 - 4.6 GPa: new perspectives on carbon transfer at subduction zones

Science.gov (United States)

Poli, S.

2013-12-01

Current knowledge on the solidus temperature for carbonate-bearing rocks suggests that carbonatitic liquids should not form in a subducted oceanic lithosphere, unless anomalous thermal relaxation occurs. For a mildly warm subduction path, COH-bearing basaltic eclogites are expected to loose all H2O component at epidote breakdown, located at approx. 2.8-3.0 GPa. Above this pressure limit, the solidus is that of a carbonated basaltic eclogite which shows a minimum temperature of 1020 °C at 4.0-4.5 GPa (Dasgupta et al. 2004). However, the oceanic crust includes a range of gabbroic rocks, altered on rifts and transforms, with large amounts of An-rich plagioclase. It has been shown that epidote disappearance with pressure depend on the normative anorthite content of the bulk composition considered (Poli et al. 2009); we therefore expect that altered gabbros might display a much wider pressure range where epidote persists, potentially affecting the solidus relationships. Notably, this applies to epidosite rocks formed in hydrothermal environments at oceanic settings, then recovered in high-pressure and ultra-high pressure terrains. New experimental data from 3.7 to 4.6 GPa, 750°C to 1000 °C are intended to unravel the effect of variable bulk and volatile compositions in model eclogites, enriched in the normative anorthite component (An37 and An45). Experiments are performed in piston cylinder and multianvil machines apparatus, using both single and, buffered, double capsule techniques. Garnet, clinopyroxene and coesite form in all syntheses. Lawsonite was found to persist at 3.7 GPa, 750 °C, with both dolomite and magnesite; at 3.8 GPa, 775-800 °C, fluid saturated conditions, epidote coexists with kyanite, dolomite and magnesite. The anhydrous assemblage garnet, omphacite, aragonite, kyanite is found at 4.2 GPa, 850 °C. At 900 °C, fluid-rich conditions, a silicate fluid/melt of granitoid composition, a carbonatitic melt and Na-carbonate are observed. Close to

Biomimetic mineralization of CaCO3 on a phospholipid monolayer: from an amorphous calcium carbonate precursor to calcite via vaterite.

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Xiao, Junwu; Wang, Zhining; Tang, Yecang; Yang, Shihe

2010-04-06

A phospholipid monolayer, approximately half the bilayer structure of a biological membrane, can be regarded as an ideal model for investigating biomineralization on biological membranes. In this work on the biomimetic mineralization of CaCO(3) under a phospholipid monolayer, we show the initial heterogeneous nucleation of amorphous calcium carbonate precursor (ACC) nanoparticles at the air-water interface, their subsequent transformation into the metastable vaterite phase instead of the most thermodynamically stable calcite phase, and the ultimate phase transformation to calcite. Furthermore, the spontaneity of the transformation from vaterite to calcite was found to be closely related to the surface tension; high surface pressure could inhibit the process, highlighting the determinant of surface energy. To understand better the mechanisms for ACC formation and the transformation from ACC to vaterite and to calcite, in situ Brewster angle microscopy (BAM), ex situ scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and X-ray diffraction analysis were employed. This work has clarified the crystallization process of calcium carbonate under phospholipid monolayers and therefore may further our understanding of the biomineralization processes induced by cellular membranes.

Intensify dodecylamine adsorption on magnesite and dolomite surfaces by monohydric alcohols

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Zhang, Hao; Liu, Wengang; Han, Cong; Wei, Dezhou