Radiation-induced catalysis of fatty acids adsorbed onto clay minerals

International Nuclear Information System (INIS)

Negron-Mendoza, A.; Ramos-Bernal, S.; Colin-Garcia, M.; Mosqueira, F.G.

2015-01-01

We studied the behavior of small fatty (acetic acid) and dicarboxylic acids (succinic and malonic acids) adsorbed onto Na + -montmorillonite (a clay mineral) and exposed to gamma radiation. A decarboxylation reaction was found to predominate when the clay was present. This preferential synthesis promoted the formation of a compound with one less carbon atom than its target compound. In the system without clay, dimerization was the predominate outcome following radiolysis. (author)

Multifaceted role of clay minerals in pharmaceuticals

OpenAIRE

Khurana, Inderpreet Singh; Kaur, Satvinder; Kaur, Harpreet; Khurana, Rajneet Kaur

2015-01-01

The desirable physical and physiochemical properties of clay minerals have led them to play a substantial role in pharmaceutical formulations. Clay minerals like kaolin, smectite and palygorskite-sepiolite are among the world's most valuable industrial minerals and of considerable importance. The elemental features of clay minerals which caused them to be used in pharmaceutical formulations are high specific area, sorption capacity, favorable rheological properties, chemical inertness, swelli...

Ground Truthing Orbital Clay Mineral Observations with the APXS Onboard Mars Exploration Rover Opportunity

Science.gov (United States)

Schroeder, C.; Gellert, R.; VanBommel, S.; Clark, B. C.; Ming, D. W.; Mittlefehldt, D. S.; Yen, A. S.

2016-01-01

NASA's Mars Exploration Rover Opportunity has been exploring approximately 22 km diameter Endeavour crater since 2011. Its rim segments predate the Hesperian-age Burns formation and expose Noachian-age material, which is associated with orbital Fe3+-Mg-rich clay mineral observations [1,2]. Moving to an orders of magnitude smaller instrumental field of view on the ground, the clay minerals were challenging to pinpoint on the basis of geochemical data because they appear to be the result of near-isochemical weathering of the local bedrock [3,4]. However, the APXS revealed a more complex mineral story as fracture fills and so-called red zones appear to contain more Al-rich clay minerals [5,6], which had not been observed from orbit. These observations are important to constrain clay mineral formation processes. More detail will be added as Opportunity is heading into her 10th extended mission, during which she will investigate Noachian bedrock that predates Endeavour crater, study sedimentary rocks inside Endeavour crater, and explore a fluid-carved gully. ESA's ExoMars rover will land on Noachian-age Oxia Planum where abundant Fe3+-Mg-rich clay minerals have been observed from orbit, but the story will undoubtedly become more complex once seen from the ground.

Feasibility of classification of clay minerals by using PAS

International Nuclear Information System (INIS)

Honda, Y; Yoshida, Y; Akiyama, Y; Nishijima, S

2015-01-01

After the nuclear power plant disaster, the evaluation of radioactive Cs kept in soil, especially in clay minerals and the elucidation of its movement are urgent subjects to promote decontamination. It is known that the extractable level of Cs depends on the sort of clay minerals. We tried to find the characteristics of clay minerals belonging to phillosilicate group using positron annihilation spectroscopy (PAS) and the relationship between the results of PAS and the amounts of substantially extracted Cs from the clay minerals. The results showed that each clay mineral was found to be distinguishable from other clay minerals by PAS and the extraction rate of Cs was different among those clay minerals, however the direct correlation between the results of PAS and the extraction rates of Cs was not found. (paper)

Adsorption of Dissolved Gases (CH4, CO2, H2, Noble Gases) by Water-Saturated Smectite Clay Minerals

Science.gov (United States)

Bourg, I. C.; Gadikota, G.; Dazas, B.

2016-12-01

Adsorption of dissolved gases by water-saturated clay minerals plays important roles in a range of fields. For example, gas adsorption in on clay minerals may significantly impact the formation of CH4 hydrates in fine-grained sediments, the behavior of CH4 in shale, CO2 leakage across caprocks of geologic CO2 sequestration sites, H2 leakage across engineered clay barriers of high-level radioactive waste repositories, and noble gas geochemistry reconstructions of hydrocarbon migration in the subsurface. Despite its importance, the adsorption of gases on clay minerals remains poorly understood. For example, some studies have suggested that clay surfaces promote the formation of CH4 hydrates, whereas others indicate that clay surfaces inhibit the formation of CH4 hydrates. Here, we present molecular dynamics (MD) simulations of the adsorption of a range of gases (CH4, CO2, H2, noble gases) on clay mineral surfaces. Our results indicate that the affinity of dissolved gases for clay mineral surfaces has a non-monotone dependence on the hydrated radius of the gas molecules. This non-monotone dependence arises from a combination of two effects: the polar nature of certain gas molecules (in particular, CO2) and the templating of interfacial water structure by the clay basal surface, which results in the presence of interfacial water "cages" of optimal size for intermediate-size gas molecules (such as Ne or Ar).

Exploring biotic vs. abiotic controls on syngenetic carbonate and clay mineral precipitation

Science.gov (United States)

Nascimento, Gabriela S.; McKenzie, Judith A.; Martinez Ruiz, Francisca; Bontognali, Tomaso R. R.; Vasconcelos, Crisogono

2016-04-01

A possible syngenetic relationship between carbonate and clay mineral precipitation has been reported for sedimentary rocks deposited in both lacustrine and marine sedimentary environments throughout the geological record. In particular, the mineral dolomite is often found associated with Mg-rich clays, such as stevensite. It is notable that this carbonate/clay association has been recorded in numerous samples taken from modern dolomite precipitating environments; for example, the Coorong lakes, South Australia, coastal sabkhas, Abu Dhabi, UAE and coastal hypersaline lagoons (Lagoa Vermelha and Brejo do Espinho) east of Rio de Janeiro, Brazil. An HRTEM study of samples from these three locations indicates a possible physical/chemical association between the Ca-dolomite and Mg-rich clays, demonstrating a probable co-precipitation. To test this hypothesis, we have conducted a series of biotic and abiotic laboratory experiments. If this syngenesis actually occurs in nature, what, if any, are the biogeochemical processes controlling these precipitation reactions? Our experiments were designed to determine the extent of the biotic versus abiotic component influencing the mineral precipitation and, in the case of a biotic influence, to understand the mechanism through which microorganisms might mediate the formation of clay minerals. The experiments were carried out in the Geomicrobiology Laboratory of ETH Zürich using cultures of living microbes and artificial organic compounds that simulate functional groups present in natural biofilms formed under both aerobic and anaerobic conditions. In addition, pure inorganic experiments were designed to understand possible physico-chemical conditions for diagenetic processes that could induce dissolution of Mg-carbonates and precipitation of Mg-rich clays. Our results show a remarkable biotic influence during the formation of clay minerals. Specifically, extracellular polymeric substances (EPS), released by microbes in their

Rates and time scales of clay-mineral formation by weathering in saprolitic regoliths of the southern Appalachians from geochemical mass balance

Science.gov (United States)

Jason R. Price; Michael A. Velbel; Lina C. Patino

2005-01-01

Rates of clay formation in three watersheds located at the Coweeta Hydrologic Laboratory, western North Carolina, have been determined from solute flux-based mass balance methods. A system of mass balance equations with enough equations and unknowns to allow calculation of secondary mineral formation rates as well as the more commonly determined primary-...

Hyperspectral analysis of clay minerals

Science.gov (United States)

Janaki Rama Suresh, G.; Sreenivas, K.; Sivasamy, R.

2014-11-01

A study was carried out by collecting soil samples from parts of Gwalior and Shivpuri district, Madhya Pradesh in order to assess the dominant clay mineral of these soils using hyperspectral data, as 0.4 to 2.5 μm spectral range provides abundant and unique information about many important earth-surface minerals. Understanding the spectral response along with the soil chemical properties can provide important clues for retrieval of mineralogical soil properties. The soil samples were collected based on stratified random sampling approach and dominant clay minerals were identified through XRD analysis. The absorption feature parameters like depth, width, area and asymmetry of the absorption peaks were derived from spectral profile of soil samples through DISPEC tool. The derived absorption feature parameters were used as inputs for modelling the dominant soil clay mineral present in the unknown samples using Random forest approach which resulted in kappa accuracy of 0.795. Besides, an attempt was made to classify the Hyperion data using Spectral Angle Mapper (SAM) algorithm with an overall accuracy of 68.43 %. Results showed that kaolinite was the dominant mineral present in the soils followed by montmorillonite in the study area.

In-situ nanoscale imaging of clay minerals with atomic force microscopy

International Nuclear Information System (INIS)

Bosbach, D.

2010-01-01

Document available in extended abstract form only. Clay minerals play a key role in many concepts for high-level nuclear waste repository systems in deep geological formations. Various aspects related to the long-term safety of nuclear disposal are linked to their fundamental physical-chemical properties, in particular with respect to their reactivity in aqueous environments. Atomic Force Microscopy (AFM) allows high resolution imaging of clay minerals in-situ while they are exposed to an aqueous solution. The presentation is intended to provide an overview of examples of AFM studies on clay minerals: 1. AFM is an ideal tool to visualize the shape of individual clay particles down to molecular scales including a quantitative description of for example their aspect ratio. Furthermore, the particle size can be easily extracted from AFM data for individual particles as well as particle size distribution. 2. Surface area of clay minerals is a key issue when discussing heterogeneous reactions such as dissolution, adsorption or (surface) precipitation - total surface area, BET surface area, reactive surface area need to be distinguished. In particular reactive surface area is linked to specific reactive surface sites. AFM is of course able to identify such sites and consequently AFM data allow to characterize and to quantify reactive surface area. 3. The reactivity of clay mineral surfaces in aqueous environments controls the behaviour of clay minerals under repository conditions and also affects the migration/retention of radionuclides. It could be shown that the dissolution of smectite particles under acidic conditions at room temperature primarily occurs at (hk0) particle edges, whereas the reactivity of the (001) basal surfaces is very limited. The heterogeneous (surface) precipitation of secondary iron (hydr)oxides phase could be unraveled by AFM observations. Surface precipitation occurs preferentially at (hk0) edges surfaces. Ignoring the surface site specific

Evaluation of the bleaching flux in clays containing hematite and different clay minerals

International Nuclear Information System (INIS)

Silva Junior, E.M.; Lusa, T.; Silva, T.M.; Medeiros, B.B.; Santos, G.R. dos; Morelli, M.R.

2016-01-01

Previous studies have shown that the addition of a synthetic flux in a clay mineral constituted by illite phase in the presence of iron oxide with the hematite, promotes color change of the firing products, making the reddish color firing into whiteness. This flow is constituted of a vitreous phase of the silicates family obtained by fusion/solidification of oxides and carbonates. Thus, the objective of this work was that of studying the interaction of the iron element in the final color mechanism of the different types of mineral crystal phase of the clays. In order to study the phenomenon, we obtained different compositions between the select clays and the synthetic flow, and characterization using X-ray diffraction (XRD) and visual analysis. The results showed that the action of the synthetic flow as a modifying agent for color depends on the mineral crystal phase of the clays. The color firing modification does not occur in the clays content high levels of kaolinite mineral phase. (author)

Clay mineral type effect on bacterial enteropathogen survival in soil.

Science.gov (United States)

Brennan, Fiona P; Moynihan, Emma; Griffiths, Bryan S; Hillier, Stephen; Owen, Jason; Pendlowski, Helen; Avery, Lisa M

2014-01-15

Enteropathogens released into the environment can represent a serious risk to public health. Soil clay content has long been known to have an important effect on enteropathogen survival in soil, generally enhancing survival. However, clay mineral composition in soils varies, and different clay minerals have specific physiochemical properties that would be expected to impact differentially on survival. This work investigated the effect of clay materials, with a predominance of a particular mineral type (montmorillonite, kaolinite, or illite), on the survival in soil microcosms over 96 days of Listeria monocytogenes, Salmonella Dublin, and Escherichia coli O157. Clay mineral addition was found to alter a number of physicochemical parameters in soil, including cation exchange capacity and surface area, and this was specific to the mineral type. Clay mineral addition enhanced enteropathogen survival in soil. The type of clay mineral was found to differentially affect enteropathogen survival and the effect was enteropathogen-specific. © 2013.

[Mechanism of tritium persistence in porous media like clay minerals].

Science.gov (United States)

Wu, Dong-Jie; Wang, Jin-Sheng; Teng, Yan-Guo; Zhang, Ke-Ni

2011-03-01

To investigate the mechanisms of tritium persistence in clay minerals, three types of clay soils (montmorillonite, kaolinite and illite) and tritiated water were used in this study to conduct the tritium sorption tests and the other related tests. Firstly, the ingredients, metal elements and heat properties of clay minerals were studied with some instrumental analysis methods, such as ICP and TG. Secondly, with a specially designed fractionation and condensation experiment, the adsorbed water, the interlayer water and the structural water in the clay minerals separated from the tritium sorption tests were fractionated for investigating the tritium distributions in the different types of adsorptive waters. Thirdly, the location and configuration of tritium adsorbed into the structure of clay minerals were studied with infrared spectrometry (IR) tests. And finally, the forces and mechanisms for driving tritium into the clay minerals were analyzed on the basis of the isotope effect of tritium and the above tests. Following conclusions have been reached: (1) The main reason for tritium persistence in clay minerals is the entrance of tritium into the adsorbed water, the interlayer water and the structural water in clay minerals. The percentage of tritium distributed in these three types of adsorptive water are in the range of 13.65% - 38.71%, 0.32% - 5.96%, 1.28% - 4.37% of the total tritium used in the corresponding test, respectively. The percentages are different for different types of clay minerals. (2) Tritium adsorbed onto clay minerals are existed in the forms of the tritiated hydroxyl radical (OT) and the tritiated water molecule (HTO). Tritium mainly exists in tritiated water molecule for adsorbed water and interlayer water, and in tritiated hydroxyl radical for structural water. (3) The forces and effects driving tritium into the clay minerals may include molecular dispersion, electric charge sorption, isotope exchange and tritium isotope effect.

Influence of composition of the raw materials on phase formation in solid compounds based on slag and clay minerals

International Nuclear Information System (INIS)

Galkin, A.V.; Tolebaev, T.; Omarova, V.I.; Burkitbaev, M.; Blynskiy, A.P.; Bachilova, N.V.; Matsynina, V.I.

2003-01-01

Full text: Activation of solidification processes in a compound formed on the basis of slag and clay minerals using sodium hydroxide - the output product from processing the BN-350 sodium coolant it is expedient to form the final product with a phase composition representing (in terms of long term storage) hydro-alumino-silicates incorporating Na-22 and Cs-137 radionuclides, which isomorphly replace other atoms in the crystal lattice sites. Combination of mineral phases, such as alkaline and alkaline-earth hydro-alumino-silicates with zeolite-like structure, providing sorptive properties, and the tobermorite like low-base hydro silicates of calcium defining the physico-mechanical properties of compound is the necessary condition for the compound stability. Investigations of phase formation in the mixtures of Kazakhstan clay, slag materials and alkali have been conducted targeted to control the physico-chemical properties of solid compound. The mixtures of alkali, thermal power plant ashes and clays of various mineralogical genesis (kaolinite, bentonite, Ca-Na-smectite montmorillonite) have been studied. The ashes and phosphorous slag while interacting with alkali are determined to form the non-alkaline hydro-silicates of stavrolite and indianite (anortite) type with free alkali being found in an unbound state. Both alkaline and alkaline-alkaline-earth hydro-silicates of Na 2 Ca 2 Si 2 O 7 H 2 O type are only formed in a compounds containing metallurgical slag. Formation of alkaline hydro-alumino-silicates of NaAlSiO 4 H 2 0 type as well as tomsonite (Na 4 Ca 8 [Al 20S i 20 O 80 ] 24H 2 O) - the zeolite like mineral have been detected in a two-component alkali-clay mixtures. Besides the quantity of tomsonite was determined to be not only dependent on Al 2 O 3 content in clay component but is also defined by stoichiometric composition of the mixture, because zeolite synthesis takes place under conditions of gels co-deposition and high pH value. Maximum quantity of

The influence of shale depositional fabric on the kinetics of hydrocarbon generation through control of mineral surface contact area on clay catalysis

Science.gov (United States)

Rahman, Habibur M.; Kennedy, Martin; Löhr, Stefan; Dewhurst, David N.; Sherwood, Neil; Yang, Shengyu; Horsfield, Brian

2018-01-01

Accurately assessing the temperature and hence the depth and timing of hydrocarbon generation is a critical step in the characterization of a petroleum system. Clay catalysis is a potentially significant modifier of hydrocarbon generation temperature, but experimental studies of clay catalysis show inconsistent or contradictory results. This study tests the hypothesis that source rock fabric itself is an influence on clay mineral catalysis as it controls the extent to which organic matter and clay minerals are physically associated. Two endmember clay-organic fabrics distinguish the source rocks studied: (1) a particulate fabric where organic matter is present as discrete, >5 μm particles and (2) a nanocomposite fabric in which amorphous organic matter is associated with clay mineral surfaces at sub-micron scale. High-resolution electron imaging and bulk geochemical characterisation confirm that samples of the Miocene Monterey Formation (California) are representative of the nanocomposite source rock endmember, whereas samples from the Permian Stuart Range Formation (South Australia) represent the particulate source rock endmember. Kinetic experiments are performed on paired whole rock and kerogen isolate samples from these two formations using open system, non-isothermal pyrolysis at three different heating rates (0.7, 2 and 5 K/min) to determine the effects of the different shale fabrics on hydrocarbon generation kinetics. Extrapolation to a modelled geological heating rate shows a 20 °C reduction in the onset temperature of hydrocarbon generation in Monterey Formation whole rock samples relative to paired kerogen isolates. This result is consistent with the Monterey Formations's nanocomposite fabric where clay catalysis can proceed because reactive clay minerals are intimately associated with organic matter. By contrast, there is no significant difference in the modelled hydrocarbon generation temperature of paired whole rock and kerogen isolates from the

Mineral acquisition from clay by budongo forest chimpanzees

NARCIS (Netherlands)

Reynolds, Vernon; Lloyd, Andrew W.; English, Christopher J.; Lyons, Peter; Dodd, Howard; Hobaiter, Catherine; Newton-Fisher, Nicholas; Mullins, Caroline; Lamon, Noemie; Schel, Anne Marijke; Fallon, Brittany

2015-01-01

Chimpanzees of the Sonso community, Budongo Forest, Uganda were observed eating clay and drinking clay-water from waterholes. We show that clay, clay-rich water, and clay obtained with leaf sponges, provide a range of minerals in different concentrations. The presence of aluminium in the clay

Characterization of clay minerals; Caracterizacion de minerales arcillosos

Energy Technology Data Exchange (ETDEWEB)

Diaz N, C.; Olguin, M.T.; Solache R, M.; Alarcon H, T.; Aguilar E, A. [Gerencia de Ciencias Basicas, Direccion de Investigacion Cientifica, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

2002-07-01

The natural clays are the more abundant minerals on the crust. They are used for making diverse industrial products. Due to the adsorption and ion exchange properties of these, a great interest for developing research directed toward the use of natural clays for the waste water treatment has been aroused. As part of such researches it is very important to carry out previously the characterization of the interest materials. In this work the results of the mineral and elemental chemical composition are presented as well as the morphological characteristics of clay minerals from different regions of the Mexican Republic. (Author)

Control of clay minerals effect in flotation. A review

Directory of Open Access Journals (Sweden)

Taner Hasan Ali

2016-01-01

Full Text Available The increased exposure to low grade ores highlights the importance of understanding phyllosilicate gangue mineralogy which consists of common gangue minerals. To improve the flotation performance and ore quality the negative effect of the clay minerals on flotation should be identified. The presence of clay minerals leads to problems, such as changing the froth stability, which are related to swelling behaviour, increase in pulp viscosity, overconsumption of reagents, slime coating and mechanical entrainment. The clay content in the ore is changing from time to time and it is necessary to provide quick solutions to the issues caused by the new ore composition. The objective of this paper is to give an overview how to control the colloidal properties of clay minerals on flotation.

Simulation of the long term alteration of clay minerals in engineered bentonite barriers: nucleation and growth of secondary clay particles

International Nuclear Information System (INIS)

Fritz, B.; Clement, A.; Zwingmann, H.; Noguera, C.

2010-01-01

Document available in extended abstract form only. The long term stability of clay rich rocks used as barriers to the migration of radionuclides in the environment of nuclear wastes has been intensively studied, looking at the geochemical interactions between clay minerals and aqueous solutions. These studies combine experimental approaches for the short term and numerical modellings for the long term extrapolations, in the frame of the research supported by ANDRA in the French design for High Level Waste (HLW) repository. The main objective of the geochemical numerical tools devoted to clay-solutions interaction processes was to predict the feed-back effects of mineralogical and chemical transformations of clay mineral, in repository conditions as defined by Andra, on their physical and transport properties (porosity, molecular diffusion, permeability). The 1D transport-reaction coupled simulation was done using the code KIRMAT, at 100 deg. C for 100000 years. The fluid considered is that of the Callovo-Oxfordian geological formation (COX) and assumed to diffuse into the clay barrier from one side. On the other side, ferrous iron, is provided by the steel overpack corrosion. Under these conditions, montmorillonite of the clay barrier is only partially transformed into illite, chlorite, and saponite. The simulation shows that only outer parts of the clay barrier is significantly modified, mainly at the interface with the geological environment. These modifications correspond to a closure of the porosity, followed by a decrease of mass transport by molecular diffusion. Near the COX, the swelling pressure of the clays from the barrier is predicted to decrease, but in its major part, the engineered barrier seems to keep its initial physical properties (porosity, molecular diffusion, permeability, swelling pressure). In this modelling approach, the very important role of secondary clay minerals has to be taken into account with relevant kinetic rate laws; particularly

Depth distribution of 137Cs adsorption property of clay minerals influenced by mineral weathering

International Nuclear Information System (INIS)

Nakao, Atsushi; Funakawa, Shinya; Kosaki, Takashi

2007-01-01

Radiocesium adsorption potential of mica clay mineral can increase as it is weathered, because K depletion in mica interlayer sites generates new Cs selective sites. However, in soils weathered under field conditions, the increase in 137 Cs adsorption potential associated with mineral weathering has not been observed extensively. We investigated four soil profiles from Japan and Thailand with different soil pH ranges (3.3-4.0, 4.2-4.3, 5.0-5.7, and 5.5-7.3). The solid/liquid distribution coefficients of Cs ( Cs Kd) in clay ( 137 Cs adsorption potential of mica clay minerals. In three soil profiles, Cs Kd value in clay was the largest at a surface horizon and was decreased with depth, whereas in the most acidic of Podzolic soil profile, it was the largest at B horizon. The large Cs Kd value in surface clays relative to deeper horizons were well associated with that of 2.0-1.0 μm clay fraction. We assumed that the 137 Cs adsorption potential increased at surface horizons mainly because coarser clay micas were weathered and generated Cs selective sites. The exceptional result obtained in Podzolic soil profile suggests that too intensive weathering destruct mica structure and may decrease in Cs adsorption potential of mica clay minerals. (author)

Paleoenvironmental Implications of Clay Minerals at Yellowknife Bay, Gale Crater, Mars

Science.gov (United States)

Bristow, Thomas F.; Blake, David F.

2014-01-01

The Mars Science Laboratory (MSL) Rover, Curiosity spent approx 150 sols at Yellowknife Bay (YKB) studying a section of fluvio-lacustrine sedimentary rocks (with potential indications of volcanic influence), informally known as the Yellowknife Bay formation. YKB lies in a distal region of the Peace Vallis alluvial fan, which extends from the northern rim of Gale Crater toward the dune field at the base of Mt Sharp. Sedimentological and stratigraphic observations are consistent with the Yellowknife Bay formation being part of a distal fan deposit, which could be as young as middle Hesperian to even early Amazonian in age (approx. 3.5 to 2.5 Ga). The Yellowknife Bay formation hosts a unit of mudstone called the Sheepbed member. Curiosity obtained powdered rock samples from two drill holes in the Sheepbed Member, named John Klein and Cumberland, and delivered them to instruments in Curiosity. Data from CheMin, a combined X-ray diffraction (XRD)/X-ray fluorescence instrument (XRF), has allowed detailed mineralogical analysis of mudstone powders revealing a clay mineral component of approx. 20 wt.% in each sample. The clay minerals are important indicators of paleoenvironmental conditions and sensitive recorders of post-depositional alteration processes. The XRD pattern of John Klein reveals a 02l band consistent with a trioctahedral phyllosilicate. A broad peak at approx. 10A with a slight inflexion at approx. 12A indicates the presence of 2:1 type clay minerals in the John Klein sample. The trioctahedral nature of the clay minerals, breadth of the basal reflection, and presence of a minor component with larger basal spacing suggests that John Klein contains a trioctahedral smectite (probably saponite), whose interlayer is largely collapsed because of the low-humidity conditions. The XRD patterns show no evidence of corrensite (mixed-layer chlorite/smectite) or chlorite, which are typical diagenetic products of trioctahedral smectites when subjected to burial and

Clay-mineral assemblages from some levels of K-118 drill core of Maha Sarakham evaporites, northeastern Thailand

Science.gov (United States)

Suwanich, Parkorn

Clay-mineral assemblages in Middle Clastic, Middle Salt, Lower Clastic, Potash Zone, and Lower Salt, totalling 13 samples from K-118 drill core, in the Maha Sarakham Formation, Khorat Basin, northeastern Thailand were studied. The clay-size particles were separated from the water-soluble salt by water leaching. Then the samples were leached again in the EDTA solution and separated into clay-size particles by using the timing sedimentation. The EDTA-clay residues were divided and analyzed by using the XRD and XRF method. The XRD peaks show that the major-clay minerals are chlorite, illite, and mixed-layer corrensite including traces of rectorite? and paragonite? The other clay-size particles are quartz and potassium feldspar. The XRF results indicate Mg-rich values and moderate MgAl atom ratio values in those clay minerals. The variable Fe, Na, and K contents in the clay-mineral assemblages can explain the environment of deposition compared to the positions of the samples from the core. Hypothetically, mineralogy and the chemistry of the residual assemblages strongly indicate that severe alteration and Mg-enrichment of normal clay detritus occurred in the evaporite environment through brine-sediment interaction. The various Mg-enrichment varies along the various members reflecting whether sedimentation is near or far from the hypersaline brine.

Geochemical study of evaporite and clay mineral-oxyhydroxide samples from the Waste Isolation Pilot Plant site

International Nuclear Information System (INIS)

Brookins, D.G.

1993-06-01

Samples of clay minerals, insoluble oxyhydroxides, and their host evaporites from the WIPP site have been studied for their major and minor elements abundances, x-ray diffraction characteristics, K-Ar ages, and Rb-Sr ages. This study was undertaken to determine their overall geochemical characteristics and to investigate possible interactions between evaporates and insoluble constituents. The evaporite host material is water-soluble, having Cl/Br ratios typical of marine evaporites, although the Br content is low. Insoluble material (usually a mixture of clay minerals and oxyhydroxide phases) yields very high Cl/Br ratios, possibly because of Cl from admixed halide minerals. This same material yields K/Rb and Th/U ratios in the normal range for shales; suggesting little, if any, effect of evaporite-induced remobilization of U, K, or Rb in the insoluble material. The rare-earth element (REE) data also show normal REE/chondrite (REE/CHON) distribution patterns, supporting the K/Rb and Th/U data. Clay minerals yield K-Ar dates in the range 365 to 390 Ma and a Rb-Sr isochron age of 428 ± 7 Ma. These ages are well in excess of the 220- to 230-Ma formational age of the evaporites, and confirm the detrital origin of the clays. The ages also show that any evaporite or clay mineral reactions that might have occurred at or near the time of sedimentation and diagenesis were not sufficient to reset the K-Ar and Rb-Sr systematics of the clay minerals. Further, x-ray data indicate a normal evaporitic assemblage of clay minerals and Fe-rich oxyhydroxide phases. The clay minerals and other insoluble material appear to be resistant to the destructive effects of their entrapment in the evaporites, which suggests that these insoluble materials would be good getters for any radionuclides (hypothetically) released from the storage of radioactive wastes in the area

Study of Adsorption of Phenanthrene on Different Types of Clay Minerals

International Nuclear Information System (INIS)

Contreras, M. L.; Escolano, O.; Rodriguez, V.; Diaz, F. J.; Perez, R.; Garcia, S.; Garcia Frutos, F. J.

2003-01-01

The fate and behaviour of non-ionic hydrophobic organic compounds in deep soil is mainly controlled by the mineral fraction present in the soil due to the very low organic carbon content of the deep soil. The mineral fraction that may greatly influence the fate and transport of these compounds due to its presence and properties are the clay minerals. Clay minerals also become increasingly important in low organic matter content soils. There tree, studies of non-ionic hydrophobic organic compounds adsorption on clay minerals without organic matter are necessary lo better understand the fate and transport of these compounds. In this work we used phenanthrene as model compound of non-ionic hydrophobic organic compound and four pure clay minerals: kaolinite, illite, montmorillonite, and vermiculite including muscovite mica. These clays minerals are selected due to its abundance in represents ve Spanish soils and different properties as its structural layers and expanding capacity. Batch experiments were performed using phenanthrene aqueous solutions and the clays selected. Phenanthrene sorption isotherms for all clays, except muscovite mica, were best described by the Freundlich model. Physical sorption on the external surfaces is the most probable adsorption mechanisms. In this sense, the presence of non-polar nano-sites on clay surfaces could determine the adsorption of phenanthrene by hydrophobic interaction on these sites. (Author) 22 refs

Hydrogen isotope ratios of clay minerals constituting clay veins found in granitic rocks in Hiroshima Prefecture

International Nuclear Information System (INIS)

Kitagawa, Ryuji; Kakitani, Satoru; Kuroda, Yoshimatsu; Matsuo, Sadao; Suzuoki, Tetsuro.

1980-01-01

The deuterium content of the constitutional and interlayer water extracted from the clay minerals (illite, montmorillonite, interstratified illite-montmorillonite mineral, kaolinite, halloysite) constituting the clay veins found in the granitic rocks in Hiroshima Prefecture was measured. The clay minerals were heated at 270 deg C to extract the interlayer water, then heated to 1,400 or 1,500 deg C to extract the constitutional water. The deuterium content of the local surface water collected from sampling points was measured. In the clay veins formed along perpendicular joints, the constituent clay minerals change from lower to upper part: illite → montmorillonite → kaolinite → halloysite. The deuterium content values of the constitutional water for illite and montmorillonite were estimated to be -67 to -69% and -86 to -89%, respectively. The deuterium content values of the constitutional water for halloysite range from -68 to -80% and for kaolinite from -63 to -67%. (J.P.N.)

Toxicological evaluation of clay minerals and derived nanocomposites: a review.

Science.gov (United States)

Maisanaba, Sara; Pichardo, Silvia; Puerto, María; Gutiérrez-Praena, Daniel; Cameán, Ana M; Jos, Angeles

2015-04-01

Clays and clay minerals are widely used in many facets of our society. This review addresses the main clays of each phyllosilicate groups, namely, kaolinite, montmorillonite (Mt) and sepiolite, placing special emphasis on Mt and kaolinite, which are the clays that are more frequently used in food packaging, one of the applications that are currently exhibiting higher development. The improvements in the composite materials obtained from clays and polymeric matrices are remarkable and well known, but the potential toxicological effects of unmodified or modified clay minerals and derived nanocomposites are currently being investigated with increased interest. In this sense, this work focused on a review of the published reports related to the analysis of the toxicological profile of commercial and novel modified clays and derived nanocomposites. An exhaustive review of the main in vitro and in vivo toxicological studies, antimicrobial activity assessments, and the human and environmental impacts of clays and derived nanocomposites was performed. From the analysis of the scientific literature different conclusions can be derived. Thus, in vitro studies suggest that clays in general induce cytotoxicity (with dependence on the clay, concentration, experimental system, etc.) with different underlying mechanisms such as necrosis/apoptosis, oxidative stress or genotoxicity. However, most of in vivo experiments performed in rodents showed no clear evidences of systemic toxicity even at doses of 5000mg/kg. Regarding to humans, pulmonary exposure is the most frequent, and although clays are usually mixed with other minerals, they have been reported to induce pneumoconiosis per se. Oral exposure is also common both intentionally and unintentionally. Although they do not show a high toxicity through this pathway, toxic effects could be induced due to the increased or reduced exposure to mineral elements. Finally, there are few studies about the effects of clay minerals on

Crude oil polycyclic aromatic hydrocarbons removal via clay-microbe-oil interactions: Effect of acid activated clay minerals.

Science.gov (United States)

Ugochukwu, Uzochukwu C; Fialips, Claire I

2017-07-01

Acid treatment of clay minerals is known to modify their properties such as increase their surface area and surface acidity, making them suitable as catalysts in many chemical processes. However, the role of these surface properties during biodegradation processes of polycyclic aromatic hydrocarbons (PAHs) is only known for mild acid (0.5 M Hydrochloric acid) treated clays. Four different clay minerals were used for this study: a montmorillonite, a saponite, a palygorskite and a kaolinite. They were treated with 3 M hydrochloric acid to produce acid activated clay minerals. The role of the acid activated montmorillonite, saponite, palygorskite and kaolinite in comparison with the unmodified clay minerals in the removal of PAHs during biodegradation was investigated in microcosm experiments. The microcosm experiments contained micro-organisms, oil, and clays in aqueous medium with a hydrocarbon degrading microorganism community predominantly composed of Alcanivorax spp. Obtained results indicated that acid activated clays and unmodified kaolinite did not enhance the biodegradation of the PAHs whereas unmodified montmorillonite, palygorskite and saponite enhanced their biodegradation. In addition, unmodified palygorskite adsorbed the PAHs significantly due to its unique channel structure. Copyright © 2017 Elsevier Ltd. All rights reserved.

The First X-ray Diffraction Patterns of Clay Minerals from Gale Crater

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Bristow, Thomas; Blake, David; Bish, David L.; Vaniman, David; Ming, Douglas W.; Morris, Richard V.; Chipera, Steve; Rampe, Elizabeth B.; Farmer, Jack, D.; Treiman, Allan H;

Distribution of Clay Minerals in Light Coal Fractions and the Thermal Reaction Products of These Clay Minerals during Combustion in a Drop Tube Furnace

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Sida Tian

2016-06-01

Full Text Available To estimate the contribution of clay minerals in light coal fractions to ash deposition in furnaces, we investigated their distribution and thermal reaction products. The light fractions of two Chinese coals were prepared using a 1.5 g·cm−3 ZnCl2 solution as a density separation medium and were burned in a drop-tube furnace (DTF. The mineral matter in each of the light coal fractions was compared to that of the relevant raw coal. The DTF ash from light coal fractions was analysed using hydrochloric acid separation. The acid-soluble aluminium fractions of DTF ash samples were used to determine changes in the amorphous aluminosilicate products with increasing combustion temperature. The results show that the clay mineral contents in the mineral matter of both light coal fractions were higher than those in the respective raw coals. For the coal with a high ash melting point, clay minerals in the light coal fraction thermally transformed more dehydroxylation products compared with those in the raw coal, possibly contributing to solid-state reactions of ash particles. For the coal with a low ash melting point, clay minerals in the light coal fraction produced more easily-slagging material compared with those in the raw coal, playing an important role in the occurrence of slagging. Additionally, ferrous oxide often produces low-melting substances in coal ash. Due to the similarities of zinc oxide and ferrous oxide in silicate reactions, we also investigated the interactions of clay minerals in light coal fractions with zinc oxide introduced by a zinc chloride solution. The extraneous zinc oxide could react, to a small extent, with clay minerals in the coal during DTF combustion.

The systems containing clays and clay minerals from modified drug release: a review.

Science.gov (United States)

Rodrigues, Luís Alberto de Sousa; Figueiras, Ana; Veiga, Francisco; de Freitas, Rivelilson Mendes; Nunes, Lívio César Cunha; da Silva Filho, Edson Cavalcanti; da Silva Leite, Cleide Maria

2013-03-01

Clays are materials commonly used in the pharmaceutical industry, either as ingredients or as active ingredients. It was observed that when they are administered concurrently, they may interact with drugs reducing their absorption. Therefore, such interactions can be used to achieve technological and biopharmaceutical advantages, regarding the control of release. This review summarizes bibliographic (articles) and technological (patents) information on the use of systems containing clays and clay minerals in modified drug delivery. In this area, formulations such natural clay, commercial clay, synthetic clay, composites clay-polymers, nanocomposites clay-polymers, films and hidrogels composites clay-polymers are used to slow/extend or vectorize the release of drugs and consequently they increase their bioavailability. Finally, this review summarizes the fields of technology and biopharmaceutical applications, where clays are applied. Copyright © 2012 Elsevier B.V. All rights reserved.

Soft X-ray spectromicroscopy study of mineral-organic matter associations in pasture soil clay fractions.

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Chen, Chunmei; Dynes, James J; Wang, Jian; Karunakaran, Chithra; Sparks, Donald L

2014-06-17

There is a growing acceptance that associations with soil minerals may be the most important overarching stabilization mechanism for soil organic matter. However, direct investigation of organo-mineral associations has been hampered by a lack of methods that can simultaneously characterize organic matter (OM) and soil minerals. In this study, STXM-NEXAFS spectroscopy at the C 1s, Ca 2p, Fe 2p, Al 1s, and Si 1s edges was used to investigate C associations with Ca, Fe, Al, and Si species in soil clay fractions from an upland pasture hillslope. Bulk techniques including C and N NEXAFS, Fe K-edge EXAFS spectroscopy, and XRD were applied to provide additional information. Results demonstrated that C was associated with Ca, Fe, Al, and Si with no separate phase in soil clay particles. In soil clay particles, the pervasive C forms were aromatic C, carboxyl C, and polysaccharides with the relative abundance of carboxyl C and polysaccharides varying spatially at the submicrometer scale. Only limited regions in the soil clay particles had aliphatic C. Good C-Ca spatial correlations were found for soil clay particles with no CaCO3, suggesting a strong role of Ca in organo-mineral assemblage formation. Fe EXAFS showed that about 50% of the total Fe in soils was contained in Fe oxides, whereas Fe-bearing aluminosilicates (vermiculite and Illite) accounted for another 50%. Fe oxides in the soil were mainly crystalline goethite and hematite, with lesser amounts of poorly crystalline ferrihydrite. XRD revealed that soil clay aluminosilicates were hydroxy-interlayered vermiculite, Illite, and kaolinite. C showed similar correlation with Fe to Al and Si, implying a similar association of Fe oxides and aluminosilicates with organic matter in organo-mineral associations. These direct microscopic determinations can help improve understanding of organo-mineral interactions in soils.

Reconstruction of a digital core containing clay minerals based on a clustering algorithm.

Science.gov (United States)

He, Yanlong; Pu, Chunsheng; Jing, Cheng; Gu, Xiaoyu; Chen, Qingdong; Liu, Hongzhi; Khan, Nasir; Dong, Qiaoling

2017-10-01

It is difficult to obtain a core sample and information for digital core reconstruction of mature sandstone reservoirs around the world, especially for an unconsolidated sandstone reservoir. Meanwhile, reconstruction and division of clay minerals play a vital role in the reconstruction of the digital cores, although the two-dimensional data-based reconstruction methods are specifically applicable as the microstructure reservoir simulation methods for the sandstone reservoir. However, reconstruction of clay minerals is still challenging from a research viewpoint for the better reconstruction of various clay minerals in the digital cores. In the present work, the content of clay minerals was considered on the basis of two-dimensional information about the reservoir. After application of the hybrid method, and compared with the model reconstructed by the process-based method, the digital core containing clay clusters without the labels of the clusters' number, size, and texture were the output. The statistics and geometry of the reconstruction model were similar to the reference model. In addition, the Hoshen-Kopelman algorithm was used to label various connected unclassified clay clusters in the initial model and then the number and size of clay clusters were recorded. At the same time, the K-means clustering algorithm was applied to divide the labeled, large connecting clusters into smaller clusters on the basis of difference in the clusters' characteristics. According to the clay minerals' characteristics, such as types, textures, and distributions, the digital core containing clay minerals was reconstructed by means of the clustering algorithm and the clay clusters' structure judgment. The distributions and textures of the clay minerals of the digital core were reasonable. The clustering algorithm improved the digital core reconstruction and provided an alternative method for the simulation of different clay minerals in the digital cores.

Reconstruction of a digital core containing clay minerals based on a clustering algorithm

Science.gov (United States)

He, Yanlong; Pu, Chunsheng; Jing, Cheng; Gu, Xiaoyu; Chen, Qingdong; Liu, Hongzhi; Khan, Nasir; Dong, Qiaoling

2017-10-01

It is difficult to obtain a core sample and information for digital core reconstruction of mature sandstone reservoirs around the world, especially for an unconsolidated sandstone reservoir. Meanwhile, reconstruction and division of clay minerals play a vital role in the reconstruction of the digital cores, although the two-dimensional data-based reconstruction methods are specifically applicable as the microstructure reservoir simulation methods for the sandstone reservoir. However, reconstruction of clay minerals is still challenging from a research viewpoint for the better reconstruction of various clay minerals in the digital cores. In the present work, the content of clay minerals was considered on the basis of two-dimensional information about the reservoir. After application of the hybrid method, and compared with the model reconstructed by the process-based method, the digital core containing clay clusters without the labels of the clusters' number, size, and texture were the output. The statistics and geometry of the reconstruction model were similar to the reference model. In addition, the Hoshen-Kopelman algorithm was used to label various connected unclassified clay clusters in the initial model and then the number and size of clay clusters were recorded. At the same time, the K -means clustering algorithm was applied to divide the labeled, large connecting clusters into smaller clusters on the basis of difference in the clusters' characteristics. According to the clay minerals' characteristics, such as types, textures, and distributions, the digital core containing clay minerals was reconstructed by means of the clustering algorithm and the clay clusters' structure judgment. The distributions and textures of the clay minerals of the digital core were reasonable. The clustering algorithm improved the digital core reconstruction and provided an alternative method for the simulation of different clay minerals in the digital cores.

Crystallite size distribution of clay minerals from selected Serbian clay deposits

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Simić Vladimir

2006-01-01

Full Text Available The BWA (Bertaut-Warren-Averbach technique for the measurement of the mean crystallite thickness and thickness distributions of phyllosilicates was applied to a set of kaolin and bentonite minerals. Six samples of kaolinitic clays, one sample of halloysite, and five bentonite samples from selected Serbian deposits were analyzed. These clays are of sedimentary volcano-sedimentary (diagenetic, and hydrothermal origin. Two different types of shape of thickness distribution were found - lognormal, typical for bentonite and halloysite, and polymodal, typical for kaolinite. The mean crystallite thickness (T BWA seams to be influenced by the genetic type of the clay sample.

Biogeochemical processes in a clay formation in situ experiment: Part F - Reactive transport modelling

Energy Technology Data Exchange (ETDEWEB)

Tournassat, Christophe, E-mail: c.tournassat@brgm.fr [BRGM, French Geological Survey, Orleans (France); Alt-Epping, Peter [Rock-Water Interaction Group, Institute of Geological Sciences, University of Bern (Switzerland); Gaucher, Eric C. [BRGM, French Geological Survey, Orleans (France); Gimmi, Thomas [Rock-Water Interaction Group, Institute of Geological Sciences, University of Bern (Switzerland)] [Laboratory for Waste Management, Paul Scherrer Institut, Villigen (Switzerland); Leupin, Olivier X. [NAGRA, CH-5430 Wettingen (Switzerland); Wersin, Paul [Gruner Ltd., CH-4020 Basel (Switzerland)

2011-06-15

Highlights: > Reactive transport modelling was used to simulate simultaneously solute transport, thermodynamic reactions, ion exchange and biodegradation during an in-situ experiment in a clay-rock formation. > Opalinus clay formation has a high buffering capacity in terms of chemical perturbations caused by bacterial activity. > Buffering capacity is mainly attributed to the carbonate system and to the reactivity of clay surfaces (cation exchange, pH buffering). - Abstract: Reactive transport modelling was used to simulate solute transport, thermodynamic reactions, ion exchange and biodegradation in the Porewater Chemistry (PC) experiment at the Mont Terri Rock Laboratory. Simulations show that the most important chemical processes controlling the fluid composition within the borehole and the surrounding formation during the experiment are ion exchange, biodegradation and dissolution/precipitation reactions involving pyrite and carbonate minerals. In contrast, thermodynamic mineral dissolution/precipitation reactions involving alumo-silicate minerals have little impact on the fluid composition on the time-scale of the experiment. With the accurate description of the initial chemical condition in the formation in combination with kinetic formulations describing the different stages of bacterial activities, it has been possible to reproduce the evolution of important system parameters, such as the pH, redox potential, total organic C, dissolved inorganic C and SO{sub 4} concentration. Leaching of glycerol from the pH-electrode may be the primary source of organic material that initiated bacterial growth, which caused the chemical perturbation in the borehole. Results from these simulations are consistent with data from the over-coring and demonstrate that the Opalinus Clay has a high buffering capacity in terms of chemical perturbations caused by bacterial activity. This buffering capacity can be attributed to the carbonate system as well as to the reactivity of

Uranyl adsorption at clay mineral surfaces

Energy Technology Data Exchange (ETDEWEB)

Roesch, N. [Technische Univ. Muenchen (Germany). Fachgebiet Theoretische Chemie

2016-11-01

This first systematic survey of actinide adsorption at complex clay mineral surfaces, which provided new insights at the atomic level, is currently being extended to neptunyl NpO{sub 2}{sup +} and more complex minerals, like iron-substituted phyllosilicates. In this way we examine if the concepts developed so far can be applied more generally to support the interpretation of pertinent experiments. A further facet of these studies is to account also for the dynamic nature of the mineral/water interface by means of exemplary dynamic simulations.

The influence of clay minerals on acoustic properties of sandstones

Energy Technology Data Exchange (ETDEWEB)

Hansen, Olav

1997-12-31

This thesis aims to provide better understanding of the relationship between the acoustic properties and the petrophysical/mineralogical properties in sand-prone rock. It emphasizes the influence of clay minerals. The author develops a method to deposit clay minerals/mineral aggregates in pore space of a rigid rock framework. Kaolinite aggregates were flushed into porous permeable Bentheimer sandstone to evaluate the effect of pore filling minerals on porosity, permeability and acoustic properties. The compressional velocity was hardly affected by the clay content and it was found that the effect of minor quantities of pore filling minerals may be acoustically modelled as an ideal suspension, where the pore fluid bulk modulus is modified by the bulk modulus of the clay minerals. The influence of clays on acoustic velocities in petroleum reservoir rocks was investigated through ultrasonic measurements of compressional- and shear-waves on core material from reservoir and non-reservoir units on the Norwegian Continental Shelf. The measured velocities decrease as the porosity increases, but are not strongly dependent on the clay content. The measured velocities are less dependent on the petrophysical and lithological properties than indicated by previous authors and published mathematical models, and stiffness reduction factors are introduced in two of the models to better match the data. Velocities are estimated along the wellbores based on non-sonic well logs and reflect well the actual sonic log well measurements. In some wells the compressional velocity cannot be modelled correctly by the models suggested. Very high compressional wave anisotropy was measured in the dry samples at atmospheric conditions. As the samples were saturated, the anisotropy was reduced to a maximum of about 30% and decreases further upon pressurization. Reservoir rocks retrieved from 2500 m are more stress dependent than those retrieved from less than 200 m depth. 168 refs., 117 figs., 24

Influence of clay minerals on curcumin properties: Stability and singlet oxygen generation

Science.gov (United States)

Gonçalves, Joyce L. S.; Valandro, Silvano R.; Poli, Alessandra L.; Schmitt, Carla C.

2017-09-01

Curcumin (CUR) has showed promising photophysical properties regarding to biological and chemical sciences. However, the main barrier for those applications are their low solubility and stability in aqueous solution. The effects of two different clay minerals, the montmorillonite (SWy-2) and the Laponite RD (Lap) nanoclay, on the stabilization of Curcumin were investigated. Their effects were compared with two well-established environments (acidic and neutral aqueous media). CUR/clay hybrids were prepared using a simple and fast method, where CUR solution was added into clay suspensions, to obtain well dispersed hybrids in water. The degradation process of CUR and CUR/clays hybrids was investigated using UV-Vis spectroscopic. For both studied hybrids, the CUR degradation process was suppressed by the presence of the clay particles. Furthermore, the Lap showed a great stabilization effect than SWy-2. This behavior was due to the smaller particle size and higher exfoliation ability of Lap, providing a large surface for CUR adsorption compared to SWy-2. The degradation process of CUR solutions and CUR/clay hybrids was also studied in the presence of light. CUR photodegradation process was faster not only in the aqueous solution but also in the clay suspension compared to those studied in the dark. The presence of clay particles accelerated the photodegradation of CUR due to the products formation in the reactions between CUR and oxygen radicals. Our results showed that the singlet oxygen quantum yield (ΦΔ) of CUR were about 59% higher in the clay suspensions than CUR in aqueous solution. Therefore, the formation of CUR/clay hybrids, in particularly with Lap, suppressed the degradation in absence light of CUR and increased the singlet oxygen generation, which makes this hybrids of CUR/clay a promising material to enlarge the application of CUR in the biological sciences.

Contrast in clay mineralogy and their effect on reservoir properties in ...

African Journals Online (AJOL)

Adigrat sandstone formation in the Blue Nile Basin is dominated by quartz arenite and subarkosic arenite, and cemented by carbonate, clay minerals and quartz overgrowths. Clay minerals in the Adigrat sandstone formation are dominated by kaolinite, illite and chlorite. Illite is the common grain-coating clay mineral.

Geochemical of clay formations : study of Spanish clay REFERENCE

International Nuclear Information System (INIS)

Turrero, M. J.; Pena, J.

2003-01-01

Clay rocks are investigated in different international research programs in order to assess its feasibility for the disposal of high level radioactive wastes. This is because different sepcific aspects: they have low hydraulic conductivity (10''-11-10''-15 m/s), a high sorption capacity, self-sealing capacity of facults and discontinuities and mechanical resistance. Several research programs on clay formations are aimed to study the chemistry of the groundwater and the water-rock reactions that control it: e. g. Boom Clay (Mol, Belgium), Oxford Clay /Harwell, United Kingdom), Toarcian Clay (Tournemire, France), Palfris formation (Wellenberg, Switzerland), Opalinus Clay (Bure, France). Based on these studies, considerable progress in the development of techniques for hydrologic, geochemical and hydrogeochemical characterization of mudstones has been accomplished (e. g. Beaufais et al. 1994, De Windt el al. 1998. Thury and Bossart 1999, Sacchi and Michelot 2000) with important advances in the knowledge of geochemical process in these materials (e. g. Reeder et al. 1993, Baeyens and Brandbury 1994, Beaucaire et al. 2000, Pearson et al., 2003).Furtermore, geochemical modeling is commonly used to simulate the evolution of water chemistry and to understand quantitatively the processes controlling the groundwater chemistry (e. g. Pearson et al. 1998, Tempel and Harrison 2000, Arcos et al., 2001). The work presented here is part of a research program funded by Enresa in the context of its R and D program. It is focused on the characterization of a clay formation (reference Argillaceous Formation, RAF) located within the Duero Basin (north-centralSpain). The characterisation of th ephysical properties,, fluid composition, mineralogy, water-rock reaction processes, geochemical modelling and sorption properties of the clays from the mentioned wells is the main purpose of this work. (Author)

Methylene blue adsorption in clay mineral dealt with organic cation

International Nuclear Information System (INIS)

Silva, T.L.; Lemos, V.P.

2011-01-01

The interaction among organic cations, as the methylene blue (AM) and benzyltrimethylammonium (BTMA), and clay minerals of the group of the smectite they result in the formation of applied materials in the adsorption of organic pollutant presents in waters, soils and you cultivate. In this work they were prepared the adsorbents (organic-clays) smectite - AM and smectite-BTMA. The precursory sample of smectite was collected in Rio Branco-Acre. We were also used an smectite sample collected in Sena Madureira (SM)-Acre already characterized in previous work and a sample of standard smectite Swy-2-Na-Montmorillonite (SWy-2) of Wymong - USA. The organic agents selected for this study they were: Blue of Methylene, denominated AM and Benzyltrimethylammonium, denominated BTMA. They were appraised the capacities adsorptive of the treated samples with BTMA being used AM as adsorbate. The results of these evaluations detected that ran total adsorption of AM (concentrations varying from 1 to 10 ppm) for the treated samples with BTMA. The organic cation, BTMA, interacting with the surfaces of the natural clay was more efficient in the adsorption of AM than the clay without the previous treatment with this salt. (author)

Influence of non-clay minerals on the interaction between metallic iron and Callovo-Oxfordian clay fraction

International Nuclear Information System (INIS)

Rivard, C.; Pelletier, M.; Villieras, F.; Michau, N.

2012-01-01

Document available in extended abstract form only. In the context of the geological disposal of high-level radioactive waste, it is of prime importance to understand the interaction mechanisms between the geological matrix, Callovo-Oxfordian clay rock (COx) and metallic iron, from the package overpack. In order to evidence the individual role of each clay component entering in the mineralogy of the COx, interactions between metallic iron and pure clays (smectites, illite and kaolinite) were first conducted. To investigate the role of the other minerals, the reactivity of COx, COx clay fraction (COxCF) and mixtures between COxCF and quartz, calcite or pyrite, was studied. Clays and additional minerals were put in contact with powder metallic iron with a weight ratio iron:clay fixed at 1:3 and a clay:solution ratio of 1:20. Proportions of non-clay minerals were deduced from the average COx composition: 50% clays, 24.5% quartz, 24.5% calcite and 1% pyrite. Batch experiments were carried out in anoxic conditions at 90 deg. C in the presence of background electrolyte (NaCl 0.02 M.L -1 , CaCl 2 0.04 M.L -1 ) in Parr reactors for durations of one, three or nine months. After reaction, solid and liquid phases were separated by centrifugation and characterized by classical techniques combining chemical analyses (liquid analyses, transmission electron microscopy combined with Energy Dispersive of X-rays spectroscopy TEM-EDS), mineralogical (X-ray diffraction), spectroscopic ( 57 Fe Moessbauer) and morphometric techniques (TEM, scanning electron microscopy and N 2 adsorption). For COx, COxCF and all the pure clay phases, major evolutions were observed during the first month, which shows that the oxidation of metallic iron is rapid in our experimental conditions. Release of iron cations in solution, pH increase (8-10) and Eh decrease (reductive conditions) are responsible for the partial dissolution of initial clay phases. Released iron is involved in the crystallization of Fe

Studies in Finishing Effects of Clay Mineral in Polymers and Synthetic Fibers

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Faheem Uddin

2013-01-01

Full Text Available The use of clay mineral in modifying the properties of polymeric material is improved in application. The current interest in modifying the polymeric materials, particularly polyethylene, polypropylene, polystyrene, and nylon using clay mineral for improved flame retardancy, thermal stability, peak heat release rate, fracture, and strength properties generated significant research literature. This paper aims to review some of the important recent modification achieved in the performance of polymeric materials using organoclay mineral. Degradation of clay mineral-polymer (nm composite is discussed with appropriate known examples. Clay mineral (nm loading of 5 wt.% to 7 wt.% that was significantly smaller than the percent loading of conventional fillers in polymeric materials introduced significant improvement in terms of thermal and physical stability. An attempt is made to emphasize flammability and thermal stability and to indicate the areas that are relatively little explored in modification of fiber-forming polymers to enhance further research interest.

Effects of magnesium minerals representative of the Callovian-Oxfordian clay-stone on borosilicate glass alteration

International Nuclear Information System (INIS)

Debure, M.

2012-01-01

Borosilicate glasses dissolution has been studied in presence of magnesium minerals. Those minerals (dolomite, illite, smectite...) belong to the Callovo-Oxfordian (COx) clay-stone layer, studied in France as a potential site for nuclear waste disposal. Such minerals contain magnesium, an element able to sustain glass alteration when it is available in solution. In the confined media of the wastes disposal, the solids reactivity controls the solution composition and can be the driving force of nuclear glass alteration. Experiments show that magnesium carbonates (hydro-magnesite and dolomite) increase in the glass alteration: the precipitation of magnesium silicates consumes silicon which slows down the formation of the glass passivating layer. The lower the magnesium mineral solubility, the lower the glass alteration. The purified clay phases (illite, smectite...) from the COx layer increase the glass alteration. Half the magnesium was replaced by sodium during the purification process. In such conditions, the effect of clay phases on glass alteration is in part due to the acidic pH-buffering effect of the clay fraction. The GRAAL model implemented in the geochemical transport code HYTEC has confirmed and quantified the mechanisms put in evidence in the experiments. Cells diffusion experiments where the two solids were separated by an inert diffusion barrier allow to valid reactive transport modelling. Such experiments are more representative of the glass package which will be separated from the COx by corrosion products. They show that glass alteration rate is reduced when solids are not close. (author) [fr

Bioremediation of PAHs and VOCs: Advances in clay mineral-microbial interaction.

Science.gov (United States)

Biswas, Bhabananda; Sarkar, Binoy; Rusmin, Ruhaida; Naidu, Ravi

2015-12-01

Bioremediation is an effective strategy for cleaning up organic contaminants, such as polycyclic aromatic hydrocarbons (PAHs) and volatile organic compounds (VOCs). Advanced bioremediation implies that biotic agents are more efficient in degrading the contaminants completely. Bioremediation by microbial degradation is often employed and to make this process efficient, natural and cost-effective materials can serve as supportive matrices. Clay/modified clay minerals are effective adsorbents of PAHs/VOCs, and readily available substrate and habitat for microorganisms in the natural soil and sediment. However, the mechanism underpinning clay-mediated biodegradation of organic compounds is often unclear, and this requires critical investigation. This review describes the role of clay/modified clay minerals in hydrocarbon bioremediation through interaction with microbial agents in specific scenarios. The vision is on a faster, more efficient and cost-effective bioremediation technique using clay-based products. This review also proposes future research directions in the field of clay modulated microbial degradation of hydrocarbons. Copyright © 2015 Elsevier Ltd. All rights reserved.

Investigating Interactions between the Silica and Carbon Cycles during Precipitation and Early Diagenesis of Authigenic Clay/Carbonate-Mineral Associations in the Carbonate Rock Record

Science.gov (United States)

McKenzie, J. A.; Francisca Martinez Ruiz, F.; Sanchez-Roman, M.; Anjos, S.; Bontognali, T. R. R.; Nascimento, G. S.; Vasconcelos, C.

2017-12-01

The study of authigenic clay/carbonate-mineral associations within carbonate sequences has important implications for the interpretation of scientific problems related with rock reservoir properties, such as alteration of potential porosity and permeability. More specifically, when clay minerals are randomly distributed within the carbonate matrix, it becomes difficult to predict reservoir characteristics. In order to understand this mineral association in the geological record, we have undertaken a comparative study of specially designed laboratory experiments with modern environments, where clay minerals have been shown to precipitate together with a range of carbonate minerals, including calcite, Mg-calcite and dolomite. Two modern dolomite-forming environments, the Coorong lakes, South Australia and Brejo do Espinho Rio de Janeiro, Brazil, were selected for this investigation. For comparative evaluation, enrichment microbial culture experiments, using natural pore water from Brejo do Espinho as the growth medium to promote mineral precipitation, were performed under both aerobic and anaerobic conditions. To establish the environmental parameters and biological processes facilitating the dual mineral association, the experimental samples have been compared with the natural minerals using HRTEM measurements. The results demonstrate that the clay and carbonate minerals apparently do not co-precipitate, but the precipitation of the different minerals in the same sample has probably occurred under different environmental conditions with variable chemistries, e.g., hypersalinity versus normal salinity resulting from the changing ratio of evaporation versus precipitation. Thus, the investigated mineral association is not a product of diagenetic processes but of sequential in situ precipitation processes related to changes in the silica and carbon availability. Implications for ancient carbonate formations will be presented and discussed in the context of a specific

Dynamic mechanical properties and anisotropy of synthetic shales with different clay minerals under confining pressure

Science.gov (United States)

Gong, Fei; Di, Bangrang; Wei, Jianxin; Ding, Pinbo; Shuai, Da

2018-03-01

The presence of clay minerals can alter the elastic behaviour of reservoir rocks significantly as the type of clay minerals, their volume and distribution, and their orientation control the shale's intrinsic anisotropic behaviours. Clay minerals are the most abundant materials in shale, and it has been proven extremely difficult to measure the elastic properties of natural shale by means of a single variable (in this case, the type of clay minerals), due to the influences of multiple factors, including water, TOC content and complex mineral compositions. We used quartz, clay (kaolinite, illite and smectite), carbonate and kerogen extract as the primary materials to construct synthetic shale with different clay minerals. Ultrasonic experiments were conducted to investigate the anisotropy of velocity and mechanical properties in dry synthetic and natural shale as a function of confining pressure. Velocities in synthetic shale are sensitive to the type of clay minerals, possibly due to the different structures of the clay minerals. The velocities increase with confining pressure and show higher rate of velocity increase at low pressures, and P-wave velocity is usually more sensitive than S-wave velocity to confining pressure according to our results. Similarly, the dynamic Young's modulus and Poisson's ratio increase with applied pressure, and the results also reveal that E11 is always larger than E33 and ν31 is smaller than ν12. Velocity and mechanical anisotropy decrease with increasing stress, and are sensitive to stress and the type of clay minerals. However, the changes of mechanical anisotropy with applied stress are larger compared with the velocity anisotropy, indicating that mechanical properties are more sensitive to the change of rock properties.

Influence of the mineral composition of clay rocks on the stability of oil wells

International Nuclear Information System (INIS)

Amorocho, P. R; Badillo, Juan

2012-01-01

In the oil companies, the operation of drilling well bore could be more expensive if the composition of the rocks is clay, the cost could increase between 10 and 15% from the starting budget. In order to decrease this problem, the oil industry has spent too much money for developing mechanisms that can provide better control and stability in clay formations during the drilling. The Society Petroleum Engineers (SPE) in some researches have published that the main chemical effects that are involved in the interaction of perforation fluids and the clay formation are: 1) chemical osmosis; and 2) hydration stresses, although, there are others like: Capillary effects, dehydration, differences in pressure and cationic exchange. These factors are not present generally in independent form. At Piedemonte Llanero the problem of the well bore stability represents a high spending of money for oil companies, caused in this region by chemical factors between fluid/rock and mechanical factors as resulted of the stresses in the area. Metil Blue Testing (MBT) and X-ray Diffraction (DR-X) were made in samples of clay; these were taken from cuts extracted of boreholes drilled in some places of the Colombian Llanos. It was found that these samples had a moderate content of reactive and low content of swell minerals.The samples main component was kaolinite, this mineral does not let the rock get swell, but it produces caving in the hole. However, it is necessary to do other tests to quantify the damages and evaluate the influence of there gime of the stress during the perforation of well bore.

Clay minerals in the sediments around the Andaman Islands

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P

on the Island proper and the slope samples show contribution from the Ganges. Distribution of detrital minerals such as quartz and feldspar support the above conclusions. The 2 distinct clay mineral provenances result because the Andaman Islands appear to be a...

Enchanted Clays: 44th Annual Meeting of the Clay Minerals Society (June 2007)

Energy Technology Data Exchange (ETDEWEB)

Randall T. Cygan

2007-06-01

“Enchanted Clays: 44th Annual Meeting of the Clay Minerals Society” was held in early June 2007 in beautiful and historic Santa Fe, New Mexico, USA. Santa Fe provided an idyllic location in the southwestern United States for the attendees to enjoy technical and social sessions while soaking up the diverse culture and wonderful climate of New Mexico—The Land of Enchantment. The meeting included a large and varied group of scientists, sharing knowledge and ideas, benefitting from technical interactions, and enjoying the wonderful historic and enchanted environs of Santa Fe. Including significant number of international scientists, the meeting was attended by approximately two hundred participants. The meeting included three days of technical sessions (oral and poster presentations), three days of field trips to clay and geological sites of northern New Mexico, and a full day workshop on the stabilization of carbon by clays. Details can be found at the meeting web site: www.sandia.gov/clay.

Clay mineral distribution on the Kerala continental shelf and slope

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P.; Nair, R.R.; Hashimi, N.H.

Seventy-five sediment samples collected from the Kerala continental shelf and slope during the 17th and 71st Cruises of @iRV gaveshani@@ were analysed by X-ray diffraction for clay mineral cntent. The distribution of total clay (< 4~k fraction...

Molecular dynamics of interfacial water and cations associated with clay minerals

International Nuclear Information System (INIS)

Cygan, Randall T.; Greathouse, Jeffery A.; Teich-McGoldrick, Stephanie L.; Nenoff, Tina M.; Daemen, Luke L.

2012-01-01

Document available in extended abstract form only. Clay mineral interfaces, including interlayer and external surfaces, play an essential role in many geochemical processes. Adsorption, dissolution, precipitation, nucleation, and growth mechanisms, in particular, are controlled by the interplay of structure, thermodynamics, kinetics, and transport at clay mineral-water interfaces. Molecular details of these geochemical processes are especially important in evaluating the fate of radionuclide waste in the environment. Such details are typically beyond the sensitivity of experimental and analytical methods and therefore require accurate models and simulations. Also, the basal surfaces and interlayers of clay minerals offer structurally constrained interfacial environments to better evaluate the local molecular chemistry. We have developed and used classical and quantum methods to examine the complex behavior of clay mineral-water interfaces and dynamics of interlayer species. Bulk structures, swelling behavior, diffusion, and adsorption processes are evaluated and compared to experimental and spectroscopic findings. In particular, inelastic neutron scattering methods provide a successful probe of vibrational behavior of interlayer species to help guide the simulations. Librations involving rock, wag, and twist motions of water molecules are particularly sensitive to the interlayer environment of smectite minerals such as montmorillonite and beidellite. Trends in librational modes for interlayer water as a function of clay structure and cation hydration energy are readily explained using structural and vibrational analysis derived from molecular simulation. Molecular dynamics simulations of virtual phases, including hydrated pyrophyllite, help to explain the behavior of interlayer water that is not associated with cation species. Additionally, we use large-scale molecular dynamics simulations of other layered minerals, such as muscovite, to evaluate adsorption

Clays and Clay Minerals and their environmental application in Food Technology

Science.gov (United States)

del Hoyo Martínez, Carmen; Cuéllar Antequera, Jorge; Sánchez Escribano, Vicente; Solange Lozano García, Marina; Cutillas Díez, Raul

2013-04-01

The clay materials have led to numerous applications in the field of public health (del Hoyo, 2007; Volzone, 2007) having been demonstrated its effectiveness as adsorbents of all contaminants. Some biodegradable materials are used for for adsorption of chemical contaminants: lignins (Valderrabano et al., 2008) and also clays and clay minerals, whose colloidal properties, ease of generating structural changes, abundance in nature, and low cost make them very suitable for this kind of applications. Among the strategies used at present to preserve the quality of the water and this way to diminish the environmental risk that supposes the chemical pollution, stands out the use of adsorbents of under cost, already they are natural or modified, to immobilize these compounds and to avoid the pollution of the water with the consequent reduction of environmental and economic costs Thanks to the development of the science and the technology of the nourishment in the last 50 years, there have revealed itself several new substances that can fulfill beneficial functions in the food, and these substances, named food additives, are today within reach of all. The food additives recover a very important role in the complex nourishing supply. The additives fulfill several useful functions in the food, which often we give for sat. Nevertheless the widespread use of food additives in the food production also influences the public health. The food industries, which are very important for the economy, spill residues proved from its activity that they have to be controlled to evaluate the environmental impact and to offer the necessary information about the quantitative evaluation of the chemical risk of the use of food additives for the public health. We have studied the adsorption of several contaminants by natural or modified clays, searching their interaction mechanisms and the possible recycling of these materials for environmental purposes and prevention of the health. References

Mineral potential of clays that cover the gypsum deposits in Araripina-PE region

International Nuclear Information System (INIS)

Lira, B.B.; Anjos, I.F. dos; Rego, S.A.B.C.

2011-01-01

In the present work the applicability of the clays that cover the deposits of Gypsum Plaster in the region of Araripina - PE for use as the ceramic pigments and for bricks production in the red ceramic industry was analyzed. The clay minerals contained the illite, kaolinite and smectite, with high proportion of the last one. The possibility of industrial application of this mineral clay is considerable; however, the mining industries that mine and process the gypsum in the region do not take the clays into account as the potential mineral. In general, industries use the clay minerals in manufacturing processes or as key raw materials, or as the alternatives for some kinds of the chemical processing industries. This paper aims to highlight the potential of materials that cover the deposits of gypsum in reference. The material sampled from different deposit layers was characterized and the physical treatment of ore was applied. The results showed that the material analyzed can be used in various kinds of industry, such as the production of natural ceramic pigments. (author)

Atom exchange between aqueous Fe(II) and structural Fe in clay minerals.

Science.gov (United States)

Neumann, Anke; Wu, Lingling; Li, Weiqiang; Beard, Brian L; Johnson, Clark M; Rosso, Kevin M; Frierdich, Andrew J; Scherer, Michelle M

2015-03-03

Due to their stability toward reductive dissolution, Fe-bearing clay minerals are viewed as a renewable source of Fe redox activity in diverse environments. Recent findings of interfacial electron transfer between aqueous Fe(II) and structural Fe in clay minerals and electron conduction in octahedral sheets of nontronite, however, raise the question whether Fe interaction with clay minerals is more dynamic than previously thought. Here, we use an enriched isotope tracer approach to simultaneously trace Fe atom movement from the aqueous phase to the solid ((57)Fe) and from the solid into the aqueous phase ((56)Fe). Over 6 months, we observed a significant decrease in aqueous (57)Fe isotope fraction, with a fast initial decrease which slowed after 3 days and stabilized after about 50 days. For the aqueous (56)Fe isotope fraction, we observed a similar but opposite trend, indicating that Fe atom movement had occurred in both directions: from the aqueous phase into the solid and from the solid into aqueous phase. We calculated that 5-20% of structural Fe in clay minerals NAu-1, NAu-2, and SWa-1 exchanged with aqueous Fe(II), which significantly exceeds the Fe atom layer exposed directly to solution. Calculations based on electron-hopping rates in nontronite suggest that the bulk conduction mechanism previously demonstrated for hematite1 and suggested as an explanation for the significant Fe atom exchange observed in goethite2 may be a plausible mechanism for Fe atom exchange in Fe-bearing clay minerals. Our finding of 5-20% Fe atom exchange in clay minerals indicates that we need to rethink how Fe mobility affects the macroscopic properties of Fe-bearing phyllosilicates and its role in Fe biogeochemical cycling, as well as its use in a variety of engineered applications, such as landfill liners and nuclear repositories.

Molecular Basis of Clay Mineral Structure and Dynamics in Subsurface Engineering Applications

Science.gov (United States)

Cygan, R. T.

2015-12-01

Clay minerals and their interfaces play an essential role in many geochemical, environmental, and subsurface engineering applications. Adsorption, dissolution, precipitation, nucleation, and growth mechanisms, in particular, are controlled by the interplay of structure, thermodynamics, kinetics, and transport at clay mineral-water interfaces. Molecular details of these processes are typically beyond the sensitivity of experimental and analytical methods, and therefore require accurate models and simulations. Also, basal surfaces and interlayers of clay minerals provide constrained interfacial environments to facilitate the evaluation of these complex processes. We have developed and used classical molecular and quantum methods to examine the complex behavior of clay mineral-water interfaces and dynamics of interlayer species. Bulk structures, swelling behavior, diffusion, and adsorption processes are evaluated and compared to experimental and spectroscopic findings. Analysis of adsorption mechanisms of radionuclides on clay minerals provides a scientific basis for predicting the suitability of engineered barriers associated with nuclear waste repositories and the fate of contaminants in the environment. Similarly, the injection of supercritical carbon dioxide into geological reservoirs—to mitigate the impact of climate change—is evaluated by molecular models of multi-fluid interactions with clay minerals. Molecular dynamics simulations provide insights into the wettability of different fluids—water, electrolyte solutions, and supercritical carbon dioxide—on clay surfaces, and which ultimately affects capillary fluid flow and the integrity of shale caprocks. This work is supported as part of Center for Frontiers of Subsurface Energy Security, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science and by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Geosciences Research Program

Determination of geochemical characters of insterstitial waters of pleistocene Italian clay formations

International Nuclear Information System (INIS)

Fontanive, A.; Gragnani, R.; Mignuzzi, C.; Spat, G.

1985-01-01

The geochemical characters of clay formations and of their pore water are fundamental with regards to the mobility of the radionuclides as well as to the corrosion processes on enginered barriers. Experimental researches have been carried out in different types of clay, which represent Italian formations, for the characterization of pore water. A squeezer system, which reaches 1500 Kg/cm 2 in pressure, and an analytical micro-scale methodology, for the determination of dissolved constituents in pore water, were set up. The extracted pore water ranges from 60% to 85% in relation to consolidation state of clay. The chemical composition of the extracted fluid has been checked during the squeezing. During this step the observed variations were smaller than those between the different specimens of the same sample. The comparison between the results obtained by squeezing and by a multiple washing technique, using increasing water/sediment ratios, shows that the last one does not give reliable results on the chemical composition of pore water. This is due to the presence of easily weatherable minerals and to the exchange processes between the clayey minerals and the solution. Nevertheless both these techniques have supplied complementary information about geochemical processes in water-rock interaction. The salinity of pore water ranges from 0.45 g/l to 24.5 g/l and the chemism always shows a high content of calcium-magnesium sulfate, or sodium chloride or calcium-magnesium-sulfate with sodium chloride. The correlation between geochemical composition of pore water and mineralogical composition of clay is not significant

Clay minerals behaviour in thin sandy clay-rich lacustrine turbidites (Lake Hazar, Turkey)

Science.gov (United States)

El Ouahabi, Meriam; Hubert-Ferrari, Aurelia; Lamair, Laura; Hage, Sophie

2017-04-01

Turbidites have been extensively studied in many different areas using cores or outcrop, which represent only an integrated snapshot of a dynamic evolving flow. Laboratory experiments provide the missing relationships between the flow characteristics and their deposits. In particular, flume experiments emphasize that the presence of clay plays a key role in turbidity current dynamics. Clay fraction, in small amount, provides cohesive strength to sediment mixtures and can damp turbulence. However, the degree of flocculation is dependent on factors such as the amount and size of clay particles, the surface of clay particles, chemistry and pH conditions in which the clay particles are dispersed. The present study focuses on thin clayey sand turbidites found in Lake Hazar (Turkey) occurring in stacked thin beds. Depositional processes and sources have been previously studied and three types were deciphered, including laminar flows dominated by cohesion, transitional, and turbulence flow regimes (Hage et al., in revision). For the purpose of determine the clay behavior in the three flow regimes, clay mineralogical, geochemical measurements on the cores allow characterising the turbidites. SEM observations provide further information regarding the morphology of clay minerals and other clasts. The study is particularly relevant given the highly alkaline and saline water of the Hazar Lake. Clay minerals in Hazar Lake sediments include kaolinite (1:1-type), illite and chlorite (2:1-type). Hazar lake water is alkaline having pH around 9.3, in such alkaline environment, a cation-exchange reaction takes place. Furthermore, in saline water (16‰), salts can act as a shield and decrease the repulsive forces between clay particle surfaces. So, pH and salt content jointly impact the behaviour of clays differently. Since the Al-faces of clay structures have a negative charge in basic solutions. At high pH, all kaolinite surfaces become negative-charged, and then kaolinite

Performance Study of the Natural Rubber Composite with Clay Minerals

International Nuclear Information System (INIS)

Nyo Nyo Myint; Tin Tin Aye; Kyaw Myo Naing; Nyunt Wynn

2008-03-01

The preparation, characterization and some applications of natural rubber clay composite have been studied. This study investigated the possibility of natural rubber latex to replace some part of natural clays. In formulation of rubber clay composite from natural rubber latex and various clay minerals, three main steps were involved (i) preparation of latex cream (ii) prevulcanization of latex cream (iii) mixing vulcanized latex compound, with other ingredients. In each step, several parameters have been carefully investigated to optimize the performance of natural rubber clay composite production. The composite products were of better quality and can be considered to be more cost effective.

Terrestrial Analogs for Clay Minerals at Yellowknife Bay, Gale Crater, Mars

Science.gov (United States)

Treiman, Allan H; Morris, Richard V.; Bristow, Thomas; Ming, Douglas W.; Achillies, Cherie; Bish, David L.; Blake, David; Vaniman, David; Chipera, Steve

2013-01-01

the last three varieties may be contemporaneous. One sample shows agate (alpha- quartz) that was precipitated between the episodes of deposition of the fine-grained and coarse-grained 'griffithite.' 'Griffithite' is not unique as a possible terrestrial analog - some clay minerals from the Doushantou formation, China, have similar 02L diffraction bands, and many basalts contain smectites in vesicles and as replacements after olivine. Similar trioctahedral smectites occur also in the nakhlite martian meteorites - as veinlets and replacements of olivine. By understanding the formation of these terrestrial clays, we hope to constrain the nature and mechanism of formation of the Sheepbed clay mineral.

Lability of soil organic carbon in tropical soils with different clay minerals

DEFF Research Database (Denmark)

Bruun, Thilde Bech; Elberling, Bo; Christensen, Bent Tolstrup

2010-01-01

Soil organic carbon (SOC) storage and turnover is influenced by interactions between organic matter and the mineral soil fraction. However, the influence of clay content and type on SOC turnover rates remains unclear, particularly in tropical soils under natural vegetation. We examined the lability...... of SOC in tropical soils with contrasting clay mineralogy (kaolinite, smectite, allophane and Al-rich chlorite). Soil was sampled from A horizons at six sites in humid tropical areas of Ghana, Malaysian Borneo and the Solomon Islands and separated into fractions above and below 250 µm by wet sieving....... Basal soil respiration rates were determined from bulk soils and soil fractions. Substrate induced respiration rates were determined from soil fractions. SOC lability was significantly influenced by clay mineralogy, but not by clay content when compared across contrasting clay minerals. The lability...

[Analysis of XRD spectral characteristics of soil clay mineral in two typical cultivated soils].

Science.gov (United States)

Zhang, Zhi-Dan; Luo, Xiang-Li; Jiang, Hai-Chao; Li, Qiao; Shen, Cong-Ying; Liu, Hang; Zhou, Ya-Juan; Zhao, Lan-Po; Wang, Ji-Hong

2014-07-01

The present paper took black soil and chernozem, the typical cultivated soil in major grain producing area of Northeast, as the study object, and determinated the soil particle composition characteristics of two cultivated soils under the same climate and location. Then XRD was used to study the composition and difference of clay mineral in two kinds of soil and the evolutionary mechanism was explored. The results showed that the two kinds of soil particles were composed mainly of the sand, followed by clay and silt. When the particle accumulation rate reached 50%, the central particle size was in the 15-130 microm interval. Except for black soil profile of Shengli Xiang, the content of clay showed converse sequence to the central particle in two soils. Clay accumulated under upper layer (18.82%) in black soil profile while under caliche layer (17.41%) in chernozem profile. Clay content was the least in parent material horizon except in black profile of Quanyanling. Analysis of clay XRD atlas showed that the difference lied in not only the strength of diffraction peak, but also in the mineral composition. The main contents of black soil and chernozem were both 2 : 1 clay, the composition of black soil was smectite/illite mixed layer-illite-vermiculite and that of chernozem was S/I mixture-illite-montmorillonite, and both of them contained little kaolinite, chlorite, quartz and other primary mineral. This paper used XRD to determine the characteristics of clay minerals comprehensively, and analyzed two kinds of typical cultivated soil comparatively, and it was a new perspective of soil minerals study.

Degradative crystal–chemical transformations of clay minerals under the influence of cyanobacterium-actinomycetal symbiotic associations

Directory of Open Access Journals (Sweden)

Ekaterina Ivanova

2014-04-01

Full Text Available Cyanobacteria and actinomycetes are essential components of soil microbial community and play an active role in ash elements leaching from minerals of the parent rock. Content and composition of clay minerals in soil determine the sorption properties of the soil horizons, water-holding capacity of the soil, stickiness, plasticity, etc. The transformative effect of cyanobacterial–actinomycetes associations on the structure of clay minerals – kaolinite, vermiculite, montmorillonite, biotite and muscovite – was observed, with the greatest structural lattice transformation revealed under the influence of association in comparison with monocultures of cyanobacterium and actinomycete. The range of the transformative effect depended both on the type of biota (component composition of association and on the crystal–chemical parameters of the mineral itself (trioctahedral mica – biotite, was more prone to microbial degradation than the dioctahedral – muscovite. The formation of the swelling phase – the product of biotite transformation into the mica–vermicullite mixed-layered formation was revealed as a result of association cultivation. Crystal chemical transformation of vermiculite was accompanied by the removal of potassium (К, magnesium (Mg and aluminum (Al from the crystal lattice. The study of such prokaryotic communities existed even in the early stages of the Earth's history helps to understand the causes and nature of the transformations undergone by the atmosphere, hydrosphere and lithosphere of the planet.contribution of treatments on structure induces and model parameters are discussed in the paper.

Clay minerals as palaeoenvironment indicators exemplified on a Karoo sequence from the Bothaville area, South Africa

International Nuclear Information System (INIS)

Buehmann, C.; Buehmann, D.

1990-01-01

The whole-rock and clay mineral composition of 74 samples from a 184 m borehole core from the Ecca Group and Dwyka Formation from the vicinity of Bothaville, 100 km southwest of Johannesburg, South Africa, has been determined by means of X-ray diffractometry. The objective was to establish the salinity and pH of the water of the original environments of deposition. The sediment investigated was subjected to a low degree of diagenesis. Clay mineral associations display characteristic variations while distinctive vertical trends in kaolinite occurrence have been established. Mineralogical trends are ascribed to fundamental changes, which must have existed in the pore fluid composition during deposition (palaeoenvironment setting) which have been maintained through the early stages of diagenesis. Conditions were alkaline-marine during the Dwyka and in the lower section of the Vryheid Formation, as indicated by the dominance of 2:1 layer silicates. From the middle section of the Vryheid Formation the entire brackish water mixing range is recorded mineralogically by kaolinite contents which increase progressively at the cost of 2:1 layer silicates. Acid-freshwater conditions, characterised by the dominance of kaolinite are interpreted for the upper section of the Vryheid Formation. 26 refs., 6 figs., 2 tabs

Significance of saturation index of certain clay minerals in shallow ...

Indian Academy of Sciences (India)

Significance of saturation index of certain clay minerals in shallow ... The value of ionic activity product (IAP) for a mineral ... where γi is the activity coefficient of ionic species ...... Domenico P A and Schwartz W 1990 Physical and Chemical.

Electron paramagnetic resonance studies on silver atoms and clusters in regularly interstratified clay minerals

International Nuclear Information System (INIS)

Yamada, H.; Tamura, K.; Shimomura, S.; Sadlo, J.; Turek, J.; Michalik, J.

2004-01-01

The formation and stabilization of reduced silver species in the regularly interstratified clay minerals, trioctahedral smectite/chlorite (tri-Sm/Ch) and dioctahedral smectite/mica (di-Sm/M), have been studied by electron paramagnetic resonance (EPR) spectroscopy. Both minerals loaded with Ag + cations after degassing and dehydration were γ-irradiated at 77 K and monitored by EPR as the temperature increased. Some samples were exposed to water or methanol vapor after dehydration. In both hydrated and dehydrated samples only the doublets to Ag 0 atoms were observed with no evidence of the formation of Ag clusters. However, the EPR parameter of silver atoms in both matrices are different. In tri-Sm/Ch the narrow anisotropic EPR lines overlap with the broader isotropic lines, whereas in di-Sm/M only broad lines are recorded. The hyperfine splitting - A iso (Ag 0 ) is larger in tri-Sm/Ch than in di-Sm/M. Also the stability of Ag 0 in both clay minerals is distinctly different. Ag 0 doublet in di-Sm/M disappears completely above 230 K, Whereas in tri-Sm/Ch it is still recorded at 310 K. It is proposed, basing on the EPR results that Ag 0 atoms appear at different sites in both matrices: - in tri-Sm/Ch in the middle of smectite interlayer and in hexagonal cavities in the silicate sheets of tetrahedron layer and in di-Sm.M in hexagonal cavities only. When samples had been exposed to methanol before irradiation, the silver clusters become stabilized in the interlayer sites. In tri-Sm/M matrix the silver dimer Ag 2 + formed by gamma-irradiation at 77 K is transformed to tetrameric cluster, Ag 4 + at 150 K. In di-Sm/M the radiation-induced silver agglomeration proceeds in a similar way, but with a slower rate and Ag tetramer is formed only above 190 K. In both clay minerals, Ag 4 + clusters decay above 250 K. (author)

Heteroaggregation of Silver Nanoparticles with Clay Minerals in Aqueous System

Science.gov (United States)

Liu, J.; Burrow, E.; Hwang, Y.; Lenhart, J.

2013-12-01

Nanoparticles are increasingly being used in industrial processes and consumer products that exploit their beneficial properties and improve our daily lives. Nevertheless, they also attract attention when released into natural environment due to their potential for causing adverse effects. The fate and transport of nanoparticles in aqueous systems have been the focus of intense study. However, their interactions with other natural particles have received only limited attention. Clay minerals are ubiquitous in most aquatic systems and their variably charged surfaces can act as deposition sites that can alter the fate and transport of nanoparticles in natural aqueous environments. In this study, we investigated the homoaggregation of silver nanoparticles with different coating layers and their heteroaggregation behavior with clay minerals (illite, kaolinite, montmorillonite) in neutral pH solutions. Silver nanoparticles with a nominal diameter of 80 nm were synthesized with three different surface coating layers: uncoated, citrate-coated and Tween-coated. Illite (IMt-2), kaolinite (KGa-2), and montmorillonite (SWy-2) were purchased from the Clay Mineral Society (Indiana) and pretreated to obtain monocationic (Na-clay) and dicationic (Ca-clay) suspensions before the experiments. The change in hydrodynamic diameter as a function of time was monitored using dynamic light scattering (DLS) measurements in order to evaluate early stage aggregation as a function of electrolyte concentration in both the homo- and heteroaggregation scenarios. A shift in the critical coagulation concentration (CCC) values to lower electrolyte concentrations was observed in binary systems, compared to single silver nanoparticle and clay systems. The results also suggest more rapid aggregation in binary system during the early aggregation stage when compared to the single-particle systems. The behavior of citrate-coated silver nanoparticles was similar to that of the bare particles, while the

Bacillus subtilis biofilm development in the presence of soil clay minerals and iron oxides.

Science.gov (United States)

Ma, Wenting; Peng, Donghai; Walker, Sharon L; Cao, Bin; Gao, Chun-Hui; Huang, Qiaoyun; Cai, Peng

2017-01-01

Clay minerals and metal oxides, as important parts of the soil matrix, play crucial roles in the development of microbial communities. However, the mechanism underlying such a process, particularly on the formation of soil biofilm, remains poorly understood. Here, we investigated the effects of montmorillonite, kaolinite, and goethite on the biofilm formation of the representative soil bacteria Bacillus subtilis . The bacterial biofilm formation in goethite was found to be impaired in the initial 24 h but burst at 48 h in the liquid-air interface. Confocal laser scanning microscopy showed that the biofilm biomass in goethite was 3-16 times that of the control, montmorillonite, and kaolinite at 48 h. Live/Dead staining showed that cells had the highest death rate of 60% after 4 h of contact with goethite, followed by kaolinite and montmorillonite. Atomic force microscopy showed that the interaction between goethite and bacteria may injure bacterial cells by puncturing cell wall, leading to the swarming of bacteria toward the liquid-air interface. Additionally, the expressions of abrB and sinR , key players in regulating the biofilm formation, were upregulated at 24 h and downregulated at 48 h in goethite, indicating the initial adaptation of the cells to minerals. A model was proposed to describe the effects of goethite on the biofilm formation. Our findings may facilitate a better understanding of the roles of soil clays in biofilm development and the manipulation of bacterial compositions through controlling the biofilm in soils.

Kinetics and Products of Chromium(VI) Reduction by Iron(II/III)-Bearing Clay Minerals.

Science.gov (United States)

Joe-Wong, Claresta; Brown, Gordon E; Maher, Kate

2017-09-05

Hexavalent chromium is a water-soluble pollutant, the mobility of which can be controlled by reduction of Cr(VI) to less soluble, environmentally benign Cr(III). Iron(II/III)-bearing clay minerals are widespread potential reductants of Cr(VI), but the kinetics and pathways of Cr(VI) reduction by such clay minerals are poorly understood. We reacted aqueous Cr(VI) with two abiotically reduced clay minerals: an Fe-poor montmorillonite and an Fe-rich nontronite. The effects of ionic strength, pH, total Fe content, and the fraction of reduced structural Fe(II) [Fe(II)/Fe(total)] were examined. The last variable had the largest effect on Cr(VI) reduction kinetics: for both clay minerals, the rate constant of Cr(VI) reduction varies by more than 3 orders of magnitude with Fe(II)/Fe(total) and is described by a linear free energy relationship. Under all conditions examined, Cr and Fe K-edge X-ray absorption near-edge structure spectra show that the main Cr-bearing product is a Cr(III)-hydroxide and that Fe remains in the clay structure after reacting with Cr(VI). This study helps to quantify our understanding of the kinetics of Cr(VI) reduction by Fe(II/III)-bearing clay minerals and may improve predictions of Cr(VI) behavior in subsurface environments.

Clay-Enriched Silk Biomaterials for Bone Formation

Science.gov (United States)

Mieszawska, Aneta J.; Llamas, Jabier Gallego; Vaiana, Christopher A.; Kadakia, Madhavi P.; Naik, Rajesh R.; Kaplan, David L.

2011-01-01

The formation of silk protein/clay composite biomaterials for bone tissue formation is described. Silk fibroin serves as an organic scaffolding material offering mechanical stability suitable for bone specific uses. Clay montmorillonite (Cloisite ® Na+) and sodium silicate are sources of osteoinductive silica-rich inorganic species, analogous to bioactive bioglass-like bone repair biomaterial systems. Different clay particle-silk composite biomaterial films were compared to silk films doped with sodium silicate as controls for support of human bone marrow derived mesenchymal stem cells (hMSCs) in osteogenic culture. The cells adhered and proliferated on the silk/clay composites over two weeks. Quantitative real-time RT-PCR analysis revealed increased transcript levels for alkaline phosphatase (ALP), bone sialoprotein (BSP), and collagen type 1 (Col I) osteogenic markers in the cells cultured on the silk/clay films in comparison to the controls. Early evidence for bone formation based on collagen deposition at the cell-biomaterial interface was also found, with more collagen observed for the silk films with higher contents of clay particles. The data suggest that the silk/clay composite systems may be useful for further study toward bone regenerative needs. PMID:21549864

Characterization of Heat-treated Clay Minerals in the Context of Nuclear Waste Disposal

Science.gov (United States)

Matteo, E. N.; Wang, Y.; Kruichak, J. N.; Mills, M. M.

2015-12-01

Clay minerals are likely candidates to aid in nuclear waste isolation due to their low permeability, favorable swelling properties, and high cation sorption capacities. Establishing the thermal limit for clay minerals in a nuclear waste repository is a potentially important component of repository design, as flexibility of the heat load within the repository can have a major impact on the selection of repository design. For example, the thermal limit plays a critical role in the time that waste packages would need to cool before being transferred to the repository. Understanding the chemical and physical changes, if any, that occur in clay minerals at various temperatures above the current thermal limit (of 100 °C) can enable decision-makers with information critical to evaluating the potential trade-offs of increasing the thermal limit within the repository. Most critical is gaining understanding of how varying thermal conditions in the repository will impact radionuclide sorption and transport in clay materials either as engineered barriers or as disposal media. A variety of repository-relevant clay minerals (illite, mixed layer illite/smectite, and montmorillonite), were heated for a range of temperatures between 100-1000 °C. These samples were characterized to determine surface area, mineralogical alteration, and cation exchange capacity (CEC). Our results show that for conditions up to 500 °C, no significant change occurs, so long as the clay mineral remains mineralogically intact. At temperatures above 500 °C, transformation of the layered silicates into silica phases leads to alteration that impacts important clay characteristics. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's Nation Nuclear Security Administration under contract DE-AC04-94AL85000. SAND Number: SAND2015-6524 A

Evaluation of the bleaching flux in clays containing hematite and different clay minerals; Avaliacao do fundente descolorante em argilas contendo hematita e diferentes argilominerais

Energy Technology Data Exchange (ETDEWEB)

Silva Junior, E.M.; Lusa, T.; Silva, T.M.; Medeiros, B.B.; Santos, G.R. dos [Universidade Tecnologica Federal do Parana (DAMEC/UFTPR), Pato Branco, PR (Brazil); Morelli, M.R., E-mail: geocrisr@utfpr.edu.com, E-mail: morelli@power.ufscar.br [Universidade Federal de Sao Carlos (DEMa/PPGCEM/UFSCar), SP (Brazil)

2016-07-01

Previous studies have shown that the addition of a synthetic flux in a clay mineral constituted by illite phase in the presence of iron oxide with the hematite, promotes color change of the firing products, making the reddish color firing into whiteness. This flow is constituted of a vitreous phase of the silicates family obtained by fusion/solidification of oxides and carbonates. Thus, the objective of this work was that of studying the interaction of the iron element in the final color mechanism of the different types of mineral crystal phase of the clays. In order to study the phenomenon, we obtained different compositions between the select clays and the synthetic flow, and characterization using X-ray diffraction (XRD) and visual analysis. The results showed that the action of the synthetic flow as a modifying agent for color depends on the mineral crystal phase of the clays. The color firing modification does not occur in the clays content high levels of kaolinite mineral phase. (author)

Preparation of Synthetic Zeolites from Myanmar Clay Mineral

International Nuclear Information System (INIS)

Phyu Phyu Win

2004-04-01

Faujasite type zeolite X was successfully synthesized from Myanmar clay mineral kaolinite, by treating with sodium hydroxide at 820 C followed by dissolution in water and hydrothermal treatment. It was found that the solution of fused clay powder can be crystallized at 90C under ambient pressure to synthesize faujasite type zeolite X. The effects of aging time and the amount of water on the formation of the product phase and Si/ Al ratios of the resulting products were investigated. Most of the Si and Al components in kaolinite might be dissolved into an alkaline solution and reacted to form ring-like structures. Then it was effectively transformed into zeolite materials. The maximum relative crystallinity of faujasite zeolite obtained was found to be 100%. Zeolite P was found to be a competitive phase present in some resulting products during hydrothermal treatment. The cation exchange capacity of kaolinite is very low, but increased after a proper treatment. It was found that the prepared faujasite type zeolite X, zeolite P and hydrogen zeolite (HZ) can reduce the hardness, the alkalinity, the total dissolved solid and the dissolved iron of raw water in the batch wise operation of water treatment. Therefore, it can be used as the cation exchanged resin for water treatment

Evaluation of the lithology contents and types of clay minerals using downhole spectral analyzer of natural gamma radiation

International Nuclear Information System (INIS)

Zivanov, M.; Savicic, M.; Grbovic, G.

1992-01-01

The microprocessor downhole spectrum analyzer of natural gamma radiation is an important part of the new generation of geophysical well logging systems. This instrument produces complete energy spectra of the penetrated formations. here physical principles of logging are shown. based on the logging results from one of the wells complex lithology was identified, together with shale contents in the formation and types of clay and minerals. (author)

Biogeochemical processes in a clay formation in situ experiment: Part E - Equilibrium controls on chemistry of pore water from the Opalinus Clay, Mont Terri Underground Research Laboratory, Switzerland

Energy Technology Data Exchange (ETDEWEB)

Pearson, F.J., E-mail: fjpearson@gmail.com [Ground-Water Geochemistry, 5108 Trent Woods Dr., New Bern, NC 28562 (United States); Tournassat, Christophe; Gaucher, Eric C. [BRGM, B.P. 36009, 45060 Orleans Cedex 2 (France)

2011-06-15

-examination of the measured Ca/Mg activity ratios and consideration of the mineralogical composition of the Opalinus Clay suggested that Ca/Mg cation exchange rather than dolomite saturation may control the ratio of these ions in solution. This re-examination also suggests that the Ca/Mg ratio decreases with increasing pore-water salinity. Several possible reasons for this are proposed. Moreover, it is demonstrated that feldspar equilibria must not be included in Opalinus Clay modelling because feldspars are present only in very small quantities in the formation and because Na/K ratios measured in pore water samples are inconsistent with feldspar saturation. The principal need to improve future modelling is additional or better data on rock properties, in particular: (i) a more detailed identification of phases in the Opalinus Clay that include redox-sensitive elements together with evaluation of their thermodynamic properties; (ii) an improved understanding of the distribution of celestite throughout the Opalinus Clay for Sr/SO{sub 4} concentrations control; (iii) improvements in analytic and thermodynamic data for Ca-Mg rock cation exchange and mineral chemical properties and (iv) the measurement of composition and stability constants of clay minerals actually present in the formation.

Adsorption and Desorption of Cesium in Clay Minerals: Effects of Natural Organic Matter and pH

Science.gov (United States)

Yoon, Hongkyu; Ilgen, Anastasia; Mills, Melissa; Lee, Moo; Seol, Jeung Gun; Cho, Nam Chan; Kang, Hyungyu

2017-04-01

Cesium (Cs) released into the environment (e.g., Fukushima accident) poses significant environmental concerns and remediation challenges. A majority of Cs in the environment have remained within the surface soils due to the strong adsorption affinity of Cs towards clay minerals. Different clay minerals have different bonding sites, resulting in various adsorption mechanisms at nanometer scale. For example, the illite commonly has a basal spacing of 1.0 nm, but becomes wider to 1.4 nm once other cations exchange with K in the interlayer site. Cs adsorbs into these expanded wedged zone strongly, which can control its mobility in the environment. In addition, natural organic matter (NOM) in the surface soils can interact with clay minerals, which can modify the mechanisms of Cs adsorption on the clay minerals by blocking specific adsorption sites and/or providing Cs adsorption sites on NOM surface. In this work, three representative clay minerals (illite, vermiculite, montmorillonite) and humic acid (HA) are used to systematically investigate the adsorption and desorption behavior of Cs. We performed batch adsorption experiments over a range of Cs concentrations on three clay minerals with and without HA, followed by sequential desorption batch testing. We tested desorption efficiency as a function of initial adsorbed Cs concentration, HA content, sodium concentration, and pH. The sequential extraction results are compared to the structural changes in clay minerals, measured using extended X-ray absorption fine structure spectroscopy (EXAFS) and aberration-corrected (scanning) transmission electron microscopy (TEM) - energy dispersive X-ray spectroscopy (EDX). Hence, this work aims to identify the mechanisms of Cs fixation at the nanometer (or atomic-) scale as a function of the clay mineral properties (e.g. expandability, permanent surface charge) and varying organic matter content at different pH values and to enhance our atomic-scale mechanistic understanding of

Isotopic exchange of 65Zn with stable Zn adsorbed on reference clay minerals

International Nuclear Information System (INIS)

Bourg, A.C.M.; Filby, R.H.

1976-01-01

For reference clays of low organic content, Zn adsorbed on the clay minerals is in kinetic equilibrium with 65 Zn in solution. Thus the specific activity approach applied to the transport of 65 Zn(II) at the water-reference clay interface is intrinsically valid. (author)

Modeling of Cation Binding in Hydrated 2:1 Clay Minerals - Final Report

International Nuclear Information System (INIS)

Smith, David E.

2000-01-01

Hydrated 2:1 clay minerals are high surface area, layered silicates that play a unique role in determining the fate of radionuclides in the environment. This project consisted of developing and implementing computer simulation methods for molecular characterization of the swelling and ion exchange properties of Hydrated 2:1 clay minerals, and the subsequent analysis and theoretical modeling with a view toward improving contaminant transport modeling as well as soil remediation and radionuclide containment strategies. Project results included the (a) development of simulation methods to treat clays under environmentally relevant conditions of variable water vapor pressure; (b) calculation of clay swelling thermodynamics as a function of interlayer ion size and charge (calculated quantities include immersion energies, free energies, and entropies of swelling); and (c) calculation of ion exchange free energies, including contributions from changing interlayer water contents and layer spacing

Thermal Behaviour of clay formations

International Nuclear Information System (INIS)

Tassoni, E.

1985-01-01

The programme carried out by ENEA to model the thermal-hydraulic-mechanical behaviour of the clay formations and to measure, in situ and in laboratory, the thermal properties of these rocks, is presented. An in situ heating experiment has been carried out in an open clay quarry in the area of Monterotondo, near Rome. The main goal of the experiment was to know the temperature field and the thermal effects caused by the high level radioactive waste disposed of in a clayey geological formation. The conclusions are as follows: - the thermal conduction codes are sufficiently accurate to forecast the temperature increases caused in the clay by the dissipation of the heat generated by high level radioactive waste; - the thermal conductivity deduced by means of the ''curve fitting'' method ranges from 0.015 to 0.017 W.cm -1 . 0 C -1 - the temperature variation associated with the transport of clay interstitial water caused by temperature gradient is negligible. A laboratory automated method has been designed to measure the thermal conductivity and diffusivity in clay samples. A review of experimental data concerning thermomechanical effects in rocks as well as results of thermal experiments performed at ISMES on clays are presented. Negative thermal dilation has been found both in the elastic and plastic range under constant stress. Thermoplastic deformation appears ten times greater than the thermoelastic one. A mathematical model is proposed in order to simulate the above and other effects that encompass thermal-elastic-plastic-pore water pressure response of clays at high temperature and effective pressure with undrained and transient drainage conditions. Implementation of the two versions into a finite element computer code is described

Clay minerals trap hydrogen in the Earth's crust: Evidence from the Cigar Lake uranium deposit, Athabasca

Science.gov (United States)

Truche, Laurent; Joubert, Gilles; Dargent, Maxime; Martz, Pierre; Cathelineau, Michel; Rigaudier, Thomas; Quirt, David

2018-07-01

Hydrogen (H2)-rich fluids are observed in a wide variety of geologic settings including gas seeps in serpentinized ultramafic rocks, sub-seafloor hydrothermal vents, fracture networks in crystalline rocks from continental and oceanic crust, and volcanic gases. Natural hydrogen sources can sustain deep microbial ecosystems, induce abiotic hydrocarbons synthesis and trigger the formation of prebiotic organic compounds. However, due to its extreme mobility and small size, hydrogen is not easily trapped in the crust. If not rapidly consumed by redox reactions mediated by bacteria or suitable mineral catalysts it diffuses through the rocks and migrates toward the surface. Therefore, H2 is not supposed to accumulate in the crust. We challenge this view by demonstrating that significant amount of H2 may be adsorbed by clay minerals and remain trapped beneath the surface. Here, we report for the first time H2 content in clay-rich rocks, mainly composed of illite, chlorite, and kaolinite from the Cigar Lake uranium ore deposit (northern Saskatchewan, Canada). Thermal desorption measurements reveal that H2 is enriched up to 500 ppm (i.e. 0.25 mol kg-1 of rock) in these water-saturated rocks having a very low total organic content (reported elsewhere for pure clay minerals or shales. Sudoite (Al-Mg di-trioctahedral chlorite) is probably the main mineral responsible for H2 adsorption in the present case. The presence of multiple binding sites in interlinked nanopores between crystal layers of illite-chlorite particles offers the ideal conditions for hydrogen sorption. We demonstrate that 4 to 17% of H2 produced by water radiolysis over the 1.4-Ga-lifetime of the Cigar Lake uranium ore deposit has been trapped in the surrounding clay alteration haloes. As a result, sorption processes on layered silicates must not be overlooked as they may exert an important control on the fate and mobility of H2 in the crust. Furthermore, the high capacity of clay minerals to sorb molecular

Development of the methodology of sample preparation to X-ray diffractometry of clay minerals at Petrobras Research Center

International Nuclear Information System (INIS)

Alves, D.B.

1987-01-01

Various procedures can be used in the analysis of the clay mineral content of rocks by X-ray diffraction. This article describes the principal ones and discusses those adopted in the X-ray clay mineral laboratory of the PETROBRAS Research Center (CENPES) in Rio de Janeiro. This article presents the methodology used and provides users with information about its application and limitations. The methodology has been developed to study polymineral samples. The aim to identify clay mineral groups and to estimate their relative proportions. Of the four main steps of this analysis - separation and concentration of clay minerals, preparation of oriented specimens, X-ray irradiation under standard conditions and interpretation of X-ray diffraction patterns - only the first three are discussed here. Clay minerals occur mainly in the [pt

Atomic force microscopy measurements of bacterial adhesion and biofilm formation onto clay-sized particles

Science.gov (United States)

Huang, Qiaoyun; Wu, Huayong; Cai, Peng; Fein, Jeremy B.; Chen, Wenli

2015-01-01

Bacterial adhesion onto mineral surfaces and subsequent biofilm formation play key roles in aggregate stability, mineral weathering, and the fate of contaminants in soils. However, the mechanisms of bacteria-mineral interactions are not fully understood. Atomic force microscopy (AFM) was used to determine the adhesion forces between bacteria and goethite in water and to gain insight into the nanoscale surface morphology of the bacteria-mineral aggregates and biofilms formed on clay-sized minerals. This study yields direct evidence of a range of different association mechanisms between bacteria and minerals. All strains studied adhered predominantly to the edge surfaces of kaolinite rather than to the basal surfaces. Bacteria rarely formed aggregates with montmorillonite, but were more tightly adsorbed onto goethite surfaces. This study reports the first measured interaction force between bacteria and a clay surface, and the approach curves exhibited jump-in events with attractive forces of 97 ± 34 pN between E. coli and goethite. Bond strengthening between them occurred within 4 s to the maximum adhesion forces and energies of −3.0 ± 0.4 nN and −330 ± 43 aJ (10−18 J), respectively. Under the conditions studied, bacteria tended to form more extensive biofilms on minerals under low rather than high nutrient conditions. PMID:26585552

Investigation of mineral composition of differently treated devonian, quaternary and triassic clays of Latvia

International Nuclear Information System (INIS)

Kosorukovs, A.; Viss, R.

1999-01-01

Clayey fractions (particle size less than 5 μm )of the Latvian Devonian (Kuprava and Liepa deposits), Quaternary (Laza and Ugale deposits) and Triassic (Akmene deposit, Republic of Lithuania) clays have been obtained. The clayey fractions were converted in the form in which all the cations were exchanged for magnesium ions. After the ion exchange the fractions were treated with dimethyl sulfoxide or glycerol in the course for two days, one sample being subjected to thermal treatment at 550±110 C for two hours. Diffractograms for the treated samples have been obtained using a DRON-2,0 diffractometer (Co-radiation). Analysis of the obtained diffractograms show that: 1) the main clayey minerals of the Devonian clays occur to be hydromicas (mainly hydromuscovite) containing admixtures of kaolinite and quartz; 2) the main clayey minerals of the Quarternary clays also occur to be hydromicas - mixtures of hydrobiotite and hydromuscovite containing admixtures of kaolinite and iron-containing chlorite; 3) smectite occurs to be the main mineral of the Triassic clay; it contains admixtures of hydromica and chlorite; 4) the Triassic and Quaternary clays contain fine- and coarse-grained carbonates, mainly calcite, in quantities of 10-16%; 5) iron and titanium are included in fine grained minerals. (author)

[Research on characteristics of soil clay mineral evolution in paddy field and dry land by XRD spectrum].

Science.gov (United States)

Zhang, Zhi-dan; Li, Qiao; Luo, Xiang-li; Jiang, Hai-chao; Zheng, Qing-fu; Zhao, Lan-po; Wang, Ji-hong

2014-08-01

The present paper took the typical saline-alkali soil in Jilin province as study object, and determinated the soil clay mineral composition characteristics of soil in paddy field and dry land. Then XRD spectrum was used to analyze the evolutionary mechanism of clay mineral in the two kinds of soil. The results showed that the physical and chemical properties of soil in paddy field were better than those in dry land, and paddy field would promote the weathering of mineral particles in saline-alkali soil and enhance the silt content. Paddy field soil showed a strong potassium-removal process, with a higher degree of clay mineral hydration and lower degree of illite crystallinity. Analysis of XRD spectrum showed that the clay mineral composition was similar in two kinds of soil, while the intensity and position of diffraction peak showed difference. The evolution process of clay mineral in dry land was S/I mixture-->vermiculite, while in paddy field it was S/I mixture-->vermiculite-->kaolinite. One kind of hydroxylated 'chlorite' mineral would appear in saline-alkali soil in long-term cultivated paddy field. Taking into account that the physical and chemical properties of soil in paddy field were better then those in dry land, we could know that paddy field could help much improve soil structure, cultivate high-fertility soil and improve saline-alkali soil. This paper used XRD spectrum to determine the characteristics of clay minerals comprehensively, and analyzed two'kinds of land use comparatively, and was a new perspective of soil minerals study.

Iodide uptake by negatively charged clay interlayers?

International Nuclear Information System (INIS)

Miller, Andrew; Kruichak, Jessica; Mills, Melissa; Wang, Yifeng

2015-01-01

Understanding iodide interactions with clay minerals is critical to quantifying risk associated with nuclear waste disposal. Current thought assumes that iodide does not interact directly with clay minerals due to electrical repulsion between the iodide and the negatively charged clay layers. However, a growing body of work indicates a weak interaction between iodide and clays. The goal of this contribution is to report a conceptual model for iodide interaction with clays by considering clay mineral structures and emergent behaviors of chemical species in confined spaces. To approach the problem, a suite of clay minerals was used with varying degrees of isomorphic substitution, chemical composition, and mineral structure. Iodide uptake experiments were completed with each of these minerals in a range of swamping electrolyte identities (NaCl, NaBr, KCl) and concentrations. Iodide uptake behaviors form distinct trends with cation exchange capacity and mineral structure. These trends change substantially with electrolyte composition and concentration, but do not appear to be affected by solution pH. The experimental results suggest that iodide may directly interact with clays by forming ion-pairs (e.g., NaI (aq) ) which may concentrate within the interlayer space as well as the thin areas surrounding the clay particle where water behavior is more structured relative to bulk water. Ion pairing and iodide concentration in these zones is probably driven by the reduced dielectric constant of water in confined space and by the relatively high polarizability of the iodide species. - Highlights: • Iodide sorption experiments were completed with a diverse array of clay minerals. • Iodide uptake trended with CEC and swamping electrolyte identity and concentration. • Results can be explained by considering the formation of ion pairs in clay interlayers

Ice nucleation efficiency of clay minerals in the immersion mode

Directory of Open Access Journals (Sweden)

V. Pinti

2012-07-01

Full Text Available Emulsion and bulk freezing experiments were performed to investigate immersion ice nucleation on clay minerals in pure water, using various kaolinites, montmorillonites, illites as well as natural dust from the Hoggar Mountains in the Saharan region. Differential scanning calorimeter measurements were performed on three different kaolinites (KGa-1b, KGa-2 and K-SA, two illites (Illite NX and Illite SE and four natural and acid-treated montmorillonites (SWy-2, STx-1b, KSF and K-10. The emulsion experiments provide information on the average freezing behaviour characterized by the average nucleation sites. These experiments revealed one to sometimes two distinct heterogeneous freezing peaks, which suggest the presence of a low number of qualitatively distinct average nucleation site classes. We refer to the peak at the lowest temperature as "standard peak" and to the one occurring in only some clay mineral types at higher temperatures as "special peak". Conversely, freezing in bulk samples is not initiated by the average nucleation sites, but by a very low number of "best sites". The kaolinites and montmorillonites showed quite narrow standard peaks with onset temperatures 238 K<T_on^std<242 K and best sites with averaged median freezing temperature T_med^best=257 K, but only some featuring a special peak (i.e. KSF, K-10, K-SA and SWy-2 with freezing onsets in the range 240–248 K. The illites showed broad standard peaks with freezing onsets at 244 K T_on^std<246 K and best sites with averaged median freezing temperature T_med^best=262 K. The large difference between freezing temperatures of standard and best sites shows that characterizing ice nucleation efficiencies of dust particles on the basis of freezing onset temperatures from bulk experiments, as has been done in some atmospheric studies, is not appropriate. Our investigations

Sorption Energy Maps of Clay Mineral Surfaces

International Nuclear Information System (INIS)

Cygan, Randall T.; Kirkpatrick, R. James

1999-01-01

A molecular-level understanding of mineral-water interactions is critical for the evaluation and prediction of the sorption properties of clay minerals that may be used in various chemical and radioactive waste disposal methods. Molecular models of metal sorption incorporate empirical energy force fields, based on molecular orbital calculations and spectroscopic data, that account for Coulombic, van der Waals attractive, and short-range repulsive energies. The summation of the non-bonded energy terms at equally-spaced grid points surrounding a mineral substrate provides a three dimensional potential energy grid. The energy map can be used to determine the optimal sorption sites of metal ions on the exposed surfaces of the mineral. By using this approach, we have evaluated the crystallographic and compositional control of metal sorption on the surfaces of kaolinite and illite. Estimates of the relative sorption energy and most stable sorption sites are derived based on a rigid ion approximation

Molecular Structural Transformation of 2:1 Clay Minerals by a Constant-Pressure Molecular Dynamics Simulation Method

International Nuclear Information System (INIS)

Wang, J.; Gutierre, M.S.

2010-01-01

This paper presents results of a molecular dynamics simulation study of dehydrated 2:1 clay minerals using the Parrinello-Rahman constant-pressure molecular dynamics method. The method is capable of simulating a system under the most general applied stress conditions by considering the changes of MD cell size and shape. Given the advantage of the method, it is the major goal of the paper to investigate the influence of imposed cell boundary conditions on the molecular structural transformation of 2:1 clay minerals under different normal pressures. Simulation results show that the degrees of freedom of the simulation cell (i.e., whether the cell size or shape change is allowed) determines the final equilibrated crystal structure of clay minerals. Both the MD method and the static method have successfully revealed unforeseen structural transformations of clay minerals upon relaxation under different normal pressures. It is found that large shear distortions of clay minerals occur when full allowance is given to the cell size and shape change. A complete elimination of the interlayer spacing is observed in a static simulation. However, when only the cell size change is allowed, interlayer spacing is retained, but large internal shear stresses also exist.

Impact of clay mineral on air oxidation of PAH-contaminated soils.

Science.gov (United States)

Biache, Coralie; Kouadio, Olivier; Lorgeoux, Catherine; Faure, Pierre

2014-09-01

This work investigated the impact of a clay mineral (bentonite) on the air oxidation of the solvent extractable organic matters (EOMs) and the PAHs from contaminated soils. EOMs were isolated from two coking plant soils and mixed with silica sand or bentonite. These samples, as well as raw soils and bentonite/soil mixtures, were oxidized in air at 60 and 100 °C for 160 days. Mineralization was followed by measuring the CO2 produced over the experiments. EOM, polycyclic aromatic compound (PAC), including PAH, contents were also determined. Oxidation led to a decrease in EOM contents and PAH concentrations, these diminutions were enhanced by the presence of bentonite. Transfer of carbon from EOM to insoluble organic matter pointed out a condensation phenomenon leading to a stabilization of the contamination. Higher mineralization rates, observed during the oxidation of the soil/bentonite mixtures, seem to indicate that this clay mineral had a positive influence on the transformation of PAC into CO2.

Clay minerals assemblage in the Neogene fluvial succession of the Pishin Belt, Pakistan

DEFF Research Database (Denmark)

Kasi, Aimal Khan; Kassi, Akhtar Muhammad; Friis, Henrik

2014-01-01

indicate derivation of material from the Pre-Miocene sedimentary and meta-sedimentary terrains of the Pishin Belt. X-ray diffraction (XRD) analyses indicate that clay minerals in various mudstones and sandstone samples are identical and detrital in nature and include smectite, chlorite, illite, serpentine...... and kaolinite. Smectite and chlorite are most probably derived from the metavolcanic and mafic volcanic rocks, respectively. Presence of serpentine in samples of the Bostan Formation indicates altered ultramafic rocks as one of the source terrains. Illite is probably recycled from the older sedimentary...

Characterization of sands and mineral clays in channel and floodplain deposits of Portuguesa river, Venezuela

Directory of Open Access Journals (Sweden)

Orlando José González Clemente

2013-11-01

Full Text Available In the main channel and floodplain of Portuguesa River were studied the mineralogical characteristics of sand and clay minerals respectively. The methodology consisted of X-ray diffraction (XRD analysis, for both mineral fractions. The results indicated the presence of mainly of quartz sands with minor amounts of chlorite, muscovite, calcite and feldspar which are considered quartz sand mature. Its origin is related to the source area and rework of soils and sediments of the floodplain. The clay fraction is characterized by the presence of 13 mineral crystalline phases consisting mainly of quartz, muscovite and chlorite, and clay minerals such as kaolinite, vermiculite, montmorillonite and nontronita. Its detrital origin may be due to mineral neoformation and inheritance. Therefore both mineral fractions consist mainly of quartz and kaolinite, which are essential components of the source area as well as the Quaternary alluvial deposits and the soils that make up the region.

Clay minerals: Properties and applications to dermocosmetic products and perspectives of natural raw materials for therapeutic purposes-A review.

Science.gov (United States)

Moraes, Jemima Daniela Dias; Bertolino, Silvana Raquel Alina; Cuffini, Silvia Lucia; Ducart, Diego Fernando; Bretzke, Pedro Eriberto; Leonardi, Gislaine Ricci

2017-12-20

Clay minerals are layered materials with a number of peculiar properties, which find many relevant applications in various industries. Since they are easily found everywhere, they are particularly attractive due to their economic viability. In the cosmetic industry, clay minerals are often used as excipients to stabilize emulsions or suspensions and to modify the rheological behavior of these systems. They also play an important role as adsorbents or absorbents, not only in cosmetics but also in other industries, such as pharmaceuticals. This reviewer believes that since this manuscript is presented as covering topical applications that include pharmaceuticals, some types of clay minerals should be considered as a potential material to be used as drug delivery systems. We review several applications of clay minerals to dermocosmetic products, relating them to the underlying properties of these materials and exemplifying with a number of clay minerals available in the market. We also discuss the use of clay minerals in topically-applied products for therapeutic purposes, specially for skin treatment and protection. Copyright © 2017 Elsevier B.V. All rights reserved.

Effects of clay mineral type and organic matter on the uptake of radiocesium by pasture plants

International Nuclear Information System (INIS)

D'Souza, T.J.

1980-10-01

Studies were undertaken to examine the influence of interaction of clay minerals and organic matter on the uptake of radiocesium by two pasture plants, namely, ryegrass (Lolium italicum L) and red clover (Trifolium pratense L). The clay minerals used were bentonite (2.1 layer type) and kaolinite (1/1 layer type). Mixtures of clay and sand were prepared with 0.5, 10, 20 and 40 per cent clay and treated with organic matter (forest turf) at 0,5 and 10 per cent of the clay-sand mixtures. Results indicated that 134 Cs uptake by plants grown on the kaolinite-clay medium was greater than that on the bentonite-clay medium at a given organic matter level. Increasing the clay content of mixtures resulted in reduction in 134 Cs uptake by both plant species. The plant uptake of 134 Cs increased with additions of organic matter at a given clay content. (author)

Fixation of Selenium by Clay Minerals and Iron Oxides

DEFF Research Database (Denmark)

Hamdy, A. A.; Nielsen, Gunnar Gissel

1977-01-01

In studying Se fixation, soil components capable of retaining Se were investigated. The importance of Fe hydrous oxides in the fixation of Se was established. The clay minerals common to soils, such as kaolinite, montmorillonite and vermiculite, all exhibited Se fixation, but greater fixation occ...

Distribution of clay minerals in the process streams produced by the extraction of bitumen from Athabasca oil sands

Energy Technology Data Exchange (ETDEWEB)

Kaminsky, H.A.W.; Etsell, T.H.; Ivey, D.G. [Alberta Univ., Edmonton, AB (Canada). Dept. of Chemical and Materials Engineering; Omotoso, O. [Natural Resources Canada, Devon, AB (Canada). CETC

2009-02-15

The clay minerals present in the oil sands were studied with particular reference to how they are partitioned in bitumen ore during the extraction process. Bitumen production from surface-mined oil sands accounts for nearly two-thirds of the total bitumen production in Alberta. Every cubic meter of mined ore results in 1.3 cubic meters of mature fine tailings (MFT). The characteristic differences between the clay minerals that report to the froth versus the tailings streams were also examined to determine which minerals could impact different unit operations in the bitumen extraction process. X-ray diffraction and random powder samples were used to quantify the clay minerals. Particle size distribution and clay activity balances were also conducted. The degree of partitioning during the conditioning and flotation stages in a batch extractor was determined by the surface properties of the clay minerals. The water-continuous tailings stream was separated into fine and coarse tailings fractions through sedimentation. The study showed that bitumen-clay interactions may be dominated by kaolinite or iron oxides. Clays are responsible for the poor settling behaviour of MFTs. The clay minerals present in the oil sands include illite, illite-smectite, kaolinite, kaolinite-smectite, and chlorite. The close proximity of the tailings ponds to the Athabasca River and volatile organic compounds (VOCs) emission require that the ponds be reclaimed to a natural landscape before mine closure. In addition to its impact on fine tailings reclamation, clay mineralogy plays a role in extraction froth flotation and emulsion stability during froth treatment. The mineralogy of the froth solids was found to be different from the mineralogy of the middlings and tailings solids. 39 refs., 6 tabs., 6 figs.

Expectations, open questions to be addressed in the workshop within the context of a deep geological repository in clay formations

International Nuclear Information System (INIS)

Landais, Patrick

2013-01-01

Precise knowledge of the clay properties in the various domains concerned by the construction feasibility, the exploitation phase of repository facilities, as well as the long term evolution of the waste and of its environment is of crucial importance in assessing the performance and the safety of the various radioactive waste disposal concepts. The knowledge to be acquired on clays as such goes well beyond solely the field of disposal of radioactive waste. For both, clay formations or bentonites in engineered barriers, the characterization in a continuous way from the nanometer to the micrometer, of their internal structure and the study of the associated physico-chemical phenomena is a fundamental issue. It aims for explaining: The 'Initial state' of the clays, in particular for the clay formations: the nature of the mechanical, hydraulic and geochemical processes, in a broad sense, and the way these processes were involved during the geological history of these formations, The fundamental processes involved by physico-chemical or hydraulic stresses, related to the evolution of the repository at the macroscopic scale. The choice of the characterization scale and relevant modeling is of first importance in the approaches leading to the establishment of the models of representation. Various research works pointed to experimental difficulties in quantifying the microstructure of the clay rocks at scales smaller than a micrometer, because of technical/instrumental limitations. This lack of knowledge at small scales does not allow to fully connect all the Thermal-hydrological-mechanical-chemical (THMC) mechanisms and to integrate them into an up-scaling approach. There already exist conceptual models and experimental approaches to describe the microstructure of argillaceous formations in terms of porosity and texture. Examples on the undisturbed Callovo-Oxfordian (COx) argillite are given in this paper. Questions and objectives to be addressed during the

Evaluation of mineral kaolinite present in portuguese clays for use in porcelain stoneware; Avaliacao do mineral caulinita presente em argilas portuguesas para uso em gres porcelanato

Energy Technology Data Exchange (ETDEWEB)

Luna da Silveira, G.C. [Instituto Federal do Rio Grande do Norte (IFRN), RN (Brazil); Acchar, W.; Gomes, U.U.; Luna da Silveira, R.V. [Universidade Federal do Rio Grnde do Norte (UFRN), RN (Brazil); Labrincha, A.; Miranda, C.M.P., E-mail: glebacoelli@hotmail.com [Universidade de Aveiro (Portugal)

2016-07-01

Kaolinite is a mineral from the kaolin, product resulting from transformation in depth of alumino silicate mineral type, such as feldspars, plagioclase and feldspars contained in the rocks. Clays are raw materials that have as main characteristic the plasticity property, which gives the product, after applying a certain pressure, a defined shape and an increase in the mechanical resistance when they become from green to dry and then to sintered. Given these characteristics, this paper analyzes the presence of the existing mineral kaolinite in two portuguese clays who are used in the preparation of formulations of porcelain stoneware tiles. The analyzes of the two clays were made by fluorescence x-ray diffraction of x-rays, thermal analysis, particle size and scanning electron microscopy, to better use of this mineral in the formulations. In both clays were found aluminum oxide, as well as mineral quartz, kaolinite and illite. (author)

Clay mineral distribution and provenance in the Heuksan mud belt, Yellow Sea

Science.gov (United States)

Cho, Hyen Goo; Kim, Soon-Oh; Kwak, Kyeong Yoon; Choi, Hunsoo; Khim, Boo-Keun

2015-12-01

The Heuksan mud belt (HMB), located in the southeastern Yellow Sea, runs parallel to the southwest coast of Korea. In this study, the distribution and relative contribution of four major clay minerals are investigated using 101 surface sediment samples collected in the course of KIOST (2001, 2010, 2011) and KIGAM (2012) cruises, as well as 33 river sediment samples (four from the Huanghe River, three from the Changjiang River, and 26 from Korean rivers) in order to clarify the provenance of fine-grained sediments in the HMB. Based on this currently largest and most robust dataset available for interpretation, the clay mineral assemblages of the fine-grained sediments in the HMB are found to be on average composed of 64.7% illite, 17.9% chlorite, 11.4% kaolinite, and 5.9% smectite. Overall, the clay mineral assemblages are similar in both the northern and the southern parts of the HMB, although smectite seems to be relatively enriched in the southern part, whereas kaolinite is slightly more dominant in the northern part. This clearly indicates that the clays are mostly derived from Korean rivers and, in the southern part of the HMB, partly also from the Huanghe River in China. The new data thus confirm and strengthen the tentative interpretation of some earlier work based on a more limited dataset.

Quality-assured evaluation of effective porosity using fit-for-purpose estimates of clay-mineral volume fraction

Science.gov (United States)

Worthington, Paul F.

2010-05-01

Reservoirs that contain dispersed clay minerals traditionally have been evaluated petrophysically using either the effective or the total porosity system. The major weakness of the former is its reliance on "shale" volume fraction ( Vsh) as a clay-mineral indicator in the determination of effective porosity from well logs. Downhole clay-mineral indicators have usually delivered overestimates of fractional clay-mineral volume ( Vcm) because they use as a reference nearby shale beds that are often assumed to comprise clay minerals exclusively, whereas those beds also include quartzitic silts and other detritus. For this reason, effective porosity is often underestimated significantly, and this shortfall transmits to computed hydrocarbons in place and thence to estimates of ultimate recovery. The problem is overcome here by using, as proxy groundtruths, core porosities that have been upscaled to match the spatial resolutions of porosity logs. Matrix and fluid properties are established over clean intervals in the usual way. Log-derived values of Vsh are tuned so that, on average, the resulting log-derived porosities match the corresponding core porosities over an evaluation interval. In this way, Vsh is rendered fit for purpose as an indicator of clay-mineral content Vcm for purposes of evaluating effective porosity. The method is conditioned to deliver a value of effective porosity that shows overall agreement with core porosity to within the limits of uncertainty of the laboratory measurements. This is achieved through function-, reservoir- and tool-specific Vsh reduction factors that can be applied to downhole estimates of clay-mineral content over uncored intervals of similar reservoir character. As expected, the reduction factors can also vary for different measurement conditions. The reduction factors lie in the range of 0.29-0.80, which means that in its raw form, log-derived Vsh can overestimate the clay-mineral content by more than a factor of three. This

Adsorption of Sr(II) on clay minerals: effects of salt concentration, loading and pH

International Nuclear Information System (INIS)

Rafferty, P.; Shiao, S.Y.; Binz, C.M.; Meyer, R.E.

1981-01-01

The adsorption of Sr(II) on a number of clay minerals has been investigated by means of a batch technique in solutions of sodium salts. Generally the results can be approximated by ideal ion exchange equations. Distribution coefficients at trace loading follow the linear relation log D = s log [Na(I)sub(aq)] + b where b is a constant and s had values of from about - 1.5 to - 2.0, which are fairly close to the ideal valve of - 2. Adsorption isotherms at constant pH and salt concentration are linear in the low loading region. Distribution coefficients for montmorillonite are almost independent of pH in the intermediate pH region 5 to 7 but for illite and kaolinite, increases in the distribution coefficient with pH are observed. Comparison of these results with literature values, insofar as it is possible, shows that distribution coefficients are usually within a factor of two or three for the same mineral with similar capacities under the same conditions even if techniques of preparation and measurement are different, but values may vary considerably more if the capacities of the different mineral samples are greatly different. Values of the distribution coefficient at very high salt concentration are very low, considerably less than unity at 4 M NaCl. Thus migration rates of Sr(II), relative to water flow, through geologic formations whose adsorption behavior is dominated by these clay minerals are likely to be high at high salt concentrations. (author)

Picloram and Aminopyralid Sorption to Soil and Clay Minerals

Science.gov (United States)

Aminopyralid sorption data are lacking, and these data are needed to predict off-target transport and plant available herbicide in soil solution. The objective of this research was to determine the sorption of picloram and aminopyralid to five soils and three clay minerals and determine if the pote...

Clay minerals and metal oxides strongly influence the structure of alkane-degrading microbial communities during soil maturation.

Science.gov (United States)

Steinbach, Annelie; Schulz, Stefanie; Giebler, Julia; Schulz, Stephan; Pronk, Geertje J; Kögel-Knabner, Ingrid; Harms, Hauke; Wick, Lukas Y; Schloter, Michael

2015-07-01

Clay minerals, charcoal and metal oxides are essential parts of the soil matrix and strongly influence the formation of biogeochemical interfaces in soil. We investigated the role of these parental materials for the development of functional microbial guilds using the example of alkane-degrading bacteria harbouring the alkane monooxygenase gene (alkB) in artificial mixtures composed of different minerals and charcoal, sterile manure and a microbial inoculum extracted from an agricultural soil. We followed changes in abundance and community structure of alkane-degrading microbial communities after 3 and 12 months of soil maturation and in response to a subsequent 2-week plant litter addition. During maturation we observed an overall increasing divergence in community composition. The impact of metal oxides on alkane-degrading community structure increased during soil maturation, whereas the charcoal impact decreased from 3 to 12 months. Among the clay minerals illite influenced the community structure of alkB-harbouring bacteria significantly, but not montmorillonite. The litter application induced strong community shifts in soils, maturated for 12 months, towards functional guilds typical for younger maturation stages pointing to a resilience of the alkane-degradation function potentially fostered by an extant 'seed bank'.

Moessbauer spectroscopy of iron in clay minerals

International Nuclear Information System (INIS)

Raclavsky, K.; Sitek, J.; Lipka, J.

1975-01-01

Selected pure clay minerals predominantly of Czechoslovak origin were studied, such as montmorillonite, nontronite, beidellite, glauconite, seladonite, illite, vermiculite, saponite, palygorskite, goethite. Moessbauer measurements were performed at room temperature with a 57 Co in Pd source. The spectra were fitted by the least square method. The parameters of the measured Moessbauer spectra are given. The values of isomer shifts, quadrupole splittings and line widths were obtained with an error of +- 0.03 mm/sec. (Z.S.)

Kinetic Study of Denatonium Sorption to Smectite Clay Minerals.

Science.gov (United States)

Crosson, Garry S; Sandmann, Emily

2013-06-01

The denatonium cation, as a benzoate salt, is the most bitter cation known to modern society and is frequently added to consumer products to reduce accidental and intentional consumption by humans and animals. Denatonium can enter the environment by accidental discharges, potentially rendering water supplies undrinkable. Interactions of denatonium with soil components ( i.e. , smectite minerals) ultimately control the environmental fate of denatonium, but the current literature is devoid of studies that evaluate denatonium sorption to smectite minerals. This study investigated the mechanism and kinetics of denatonium sorption to smectite clay minerals as a function of smectite type, temperature, pH and ionic strength. Uptake by synthetic mica montmorillonite (Syn-1), Wyoming montmorillonite (SWy-2), and Texas montmorillonite (STx-1b) at 305K was rapid, with equilibrium being reached within 2 min for all clays. Complete removal of denatonium was observed for STx-1b at pH 6.9, while partial removal was observed for Syn-1 and SWy-2. Kinetic behavior of SWy-2 and Syn-1 is consistent with a pseudo-second-order model at 305K. An activation energy of +25.9 kJ/mol was obtained for sorption to Syn-1 and was independent of temperature between 286K and 338K. Activation-free energy (Δ G *), activation enthalpy (Δ H *), and activation entropy (Δ S *) for Syn-1 were found to be +62.91 kJ/mol, +23.36 kJ/mol, and -0.130 kJ/(K·mol), respectively. Sorption capacities at pH 3.6, 6.9, and 8.2 were constant at 1.3×10 -2 g denatonium/g clay; however, the kinetic rate constant increased by 56%, going from acidic to basic solution conditions. Distribution coefficients were negatively correlated with ionic strength, suggesting cation exchange. Collectively, results suggested that smectite minerals can serve as efficient sinks for denatonium cations. This is much-needed information for agencies developing regulations regarding denatonium usage and for water treatment professionals

The redox properties of the natural iron-bearing clay mineral ferruginous smectite SWA-1: a combined electrochemical and spectroscopic study

International Nuclear Information System (INIS)

Gorski, Christopher A.; Voegelin, Andreas; Sander, Michael; Hofstetter, Thomas B.

2012-01-01

Document available in extended abstract form only. Iron-bearing clay minerals are ubiquitous in the environment and clay-mineral-based materials have been proposed to be part of backfill material in nuclear waste repositories. Laboratory and field studies have confirmed that structural iron (Fe) in clay minerals participates in redox reactions with organic pollutants, metals, and radionuclides, thus influencing their transport and reactivity. Knowledge of the redox properties of Fe-bearing clay minerals is therefore essential for understanding and predicting the fate, mobility, and bioavailability subsurface contaminants. A quantitative understanding of clay mineral redox behavior remains lacking, however, due to constraints in previous experimental approaches and the complex structural changes that accompany changes in the Fe oxidation state. This work provides a quantitative means for measuring the redox properties of Fe-bearing clay minerals, which can be applied to both field and laboratory studies tracking radionuclide-clay mineral redox reactions. Here we use mediated electrochemical reduction and oxidation to determine the electron accepting and donating capacities of several natural Fe-bearing clay minerals with different structural Fe content (2.3 to 21 wt-%) and varied redox histories. Results indicate that the fraction of redox-active Fe in clay minerals is mineral-dependent, and is linked to the thermodynamics of reduction and oxidation as well as to the ability of clay minerals to conduct electrons and facilitate structural re-arrangements required to maintain charge balance. The reduction potential (E H ) characteristics of a natural ferruginous smectite (SWa-1) were further characterized as a function of solution conditions and repeated Fe reduction and oxidation cycles. SWa-1 samples were analyzed with Moessbauer spectroscopy (MS) and X-ray absorption spectroscopy (XAS) to link observed redox potential behavior to structural properties and changes

Method and apparatus for determining characteristics of clay-bearing formations

International Nuclear Information System (INIS)

Fertl, W.H.; Ruhovets, N.

1986-01-01

This invention relates to methods and apparatus for determining characteristics of clay-bearing geological formations by radioactivity well logging. In its broadest aspect, the invention comprises the steps of determining the volume of clay contained in the earth formations; determining a first property of the formations functionally related to the volume of clay; and determining a second property functionally related to the first property, the second property indicating potential clay swelling. In particular, the volume of clay is determined using electrical signals generated in response to the energy and frequency of detected radiations. The method is carried out with a well logging instrument that includes a high-resolution gamma ray spectrometer that traverses a borehole, whereby natural radiation strikes a scintillation crystal contained therein

Study of adsorption of Phenanthrene on Different Types of Clay Minerals; Estudio de Adsorcion de Fenentreno en Diferentes Tipos de Arcillas

Energy Technology Data Exchange (ETDEWEB)

Contreras, M L; Escolano, O; Rodriguez, V; Diaz, F J; Perez, R; Garcia, S; Garcia Frutos, F J

2003-07-01

The fate and behaviour of non-ionic hydrophobic organic compounds in deep soil is mainly controlled by the mineral fraction present in the soil due to the very low organic carbon content of the deep soil. The mineral fraction that may greatly influence the fate and transport of these compounds due to its presence and properties are the clay minerals. Clay mineral also become increasingly important in low organic matter content soils. There tree, studies of non-ionic hydrophobic organic compounds adsorption on clay minerals without organic matter are necessary lo better understand the fate and transport of these compounds. In this work we used phenanthrene as model compound of non-ionic hydrophobic organic compound and four pure clay minerals: kaolinite, illite, montmorillonite, and vermiculite including muscovite mica. These clays minerals are selected due to its abundance in represent ve Spanish soils and different properties as its structural layers and expanding capacity. Batch experiments were performed using phenanthrene aqueous solutions and the clays selected. Phenanthrene sorption isotherms for all clays, except muscovite mica, were best described by the Freundlich model. Physical sorption on the external surfaces is the most probable adsorption mechanisms. In this sense, the presence of non-polar nano-sites on clay surfaces could determine the adsorption of phenanthrene by hydrophobic interaction on these sites. (Author) 22 refs.

Clay mineral distribution on tropical shelf: an example from the western shelf of India

Digital Repository Service at National Institute of Oceanography (India)

Hashimi, N.H.; Nair, R.R.

Seventy-five sediment samples collected from the Kerala continental shelf and slope during the 17th and 71st Cruises of RV Gaveshani were analysed by X-ray diffraction for clay mineral content. The distribution of total clay ( 4 mu fraction...

Soil Microbes and soil microbial proteins: interactions with clay minerals

International Nuclear Information System (INIS)

Spence, A.; Kelleher, B. P.

2009-01-01

Bacterial enumeration in soil environments estimates that the population may reach approximately 10 1 0 g - 1 of soil and comprise up to 90% of the total soil microbial biomass. Bacteria are present in soils as single cells or multicell colonies and often strongly adsorb onto mineral surfaces such as sand and clay. The interactions of microbes and microbial biomolecules with these minerals have profound impacts on the physical, chemical and biological properties of soils. (Author)

Fluorescence X-ray microscopy on hydrated tributyltin-clay mineral suspensions

Science.gov (United States)

Neuhäusler, U.; Schmidt, C.; Hoch, M.; Susini, J.

2003-03-01

Using the scanning transmission X-ray microscope at ID21 beamline of the ESRF in fluorescence mode, we mapped tin at a bulk concentration of 1000 μg(Sn)/ml within hydrated tributyltin (TBT)-clay mineral (Kaolinite) dispersion with sub-300 nm spatial resolution. Using the L absorption edges of tin at 3929, 4156 and 4465 eV fluorescence radiation was excited in tin atoms with incident photon energies of 4 and 4.5 keV. When using 4 keV radiation, only tin fluorescence is excited. For 4.5 keV X rays, both the fluorescence of tin and calcium (which is present in the solid phase) can be measured. Methodologically, we were interested in assessing and proving the possibilities and limitations of fluorescence mapping using the L absorption edges of tin, where the fluorescence yield is significantly lower compared to other elements with their K edges in the same energy range. Scientifically, organotin-clay mineral interactions are of environmental concern because this factor influences significantly the distribution of toxic TBT in the aquatic System. On one hand, the half-life of TBT deposited to the sediment phase increases, and consequently the time of its bioavailability. On the other hand, the adsorption process is reversible, which means that contaminated sediments can act as a source of pollution. The adsorption and desorption effects can be studied directly with high spatial resolution and brought into connection to the surface properties of the clay mineral under study as well as to other experimental parameters, like pH or salinity.

Phase transformations of pyrophyllite clay mineral after heat treatment

International Nuclear Information System (INIS)

Salvadori, M.C.

1988-01-01

The termal transformation of the Pyrophyllite clay mineral, given by the equations: AL sub(2) O sub(3).4SiO sub(2).H sub(2) O → Al sub(2) O sub(3).4SiO sub(2) + H sub(2) O Pyrophyllite Anhydride Water vapour. 3 (Al sub(2) O sub(3).4SiO sub(2)) → 3 Al sub(2) O sub(3). 2SiO sub(2) + 10 (SiO sub(2)) Pyrophyllite Anhydride Mullite Cristobalite, were studied by Transmission Electron Microscopy (TEM) associated to Selected Area Electron Diffraction (SAD), applied to a very pure sample, colected at Diamantina, M.G. Some other tgechniques were also used, as X-ray Diffraction (XRD), Differential Thermal Analysis (DTA) and Thermogravimetric Analysis (TGA), applied to other different Pyrophyllite samples. A thermodynamical theoretical study was undertaken to estimate the values for the entropyu of formation, enthalpy and molar thermal capacity for the Pyrophyllite Anhydride. (author)

Stochastic Approach to Determine CO2 Hydrate Induction Time in Clay Mineral Suspensions

Science.gov (United States)

Lee, K.; Lee, S.; Lee, W.

2008-12-01

A large number of induction time data for carbon dioxide hydrate formation were obtained from a batch reactor consisting of four independent reaction cells. Using resistance temperature detector(RTD)s and a digital microscope, we successfully monitored the whole process of hydrate formation (i.e., nucleation and crystal growth) and detected the induction time. The experiments were carried out in kaolinite and montmorillonite suspensions at temperatures between 274 and 277 K and pressures ranging from 3.0 to 4.0 MPa. Each set of data was analyzed beforehand whether to be treated by stochastic manner or not. Geochemical factors potentially influencing the hydrate induction time under different experimental conditions were investigated by stochastic analyses. We observed that clay mineral type, pressure, and temperature significantly affect the stochastic behavior of the induction times for CO2 hydrate formation in this study. The hydrate formation kinetics along with stochastic analyses can provide basic understanding for CO2 hydrate storage in deep-sea sediment and geologic formation, securing its stability under the environments.

Adsorption Properties of Hydrocarbons (n-Decane, Methyl Cyclohexane and Toluene on Clay Minerals: An Experimental Study

Directory of Open Access Journals (Sweden)

Jie Zhang

2017-10-01

Full Text Available Adsorption of hydrocarbons may significantly affect hydrocarbon migration in unconventional reservoirs. Clay minerals form the primary adsorbent surfaces for hydrocarbons adsorbed in mudstone/shale. To study the adsorption properties of hydrocarbons (n-decane (C10H22, methyl cyclohexane (C7H14 and toluene (C7H8 on clay minerals (i.e., cookeite, ripidolite, kaolinite, illite, illite/smectite mixed-layer, Na-montmorillonite and Ca-montmorillonite, hydrocarbon vapor adsorption (HVA tests were conducted at 298.15 K. The results showed that (i the adsorption amounts of C10H22, C7H14 and C7H8 ranged from 0.45–1.03 mg/m2, 0.28–0.90 mg/m2 and 0.16–0.53 mg/m2, respectively; (ii for cookeite, ripidolite and kaolinite, the adsorption capacity of C10H22 was less than C7H14, which was less than C7H8; (iii for illite, Na-montmorillonite and Ca-montmorillonite, the adsorption capacity of C10H22 was greater than that of C7H8, and the adsorption capacity of C7H14 was the lowest; (iv for an illite/smectite mixed-layer, C7H14 had the highest adsorption capacity, followed by C10H22, and C7H8 had the lowest capacity. Adsorption properties were correlated with the microscopic parameters of pores in clay minerals and with experimental pressure. Finally, the weighted average method was applied to evaluate the adsorption properties of C10H22, C7H14 and C7H8 on clay minerals in oil-bearing shale from the Shahejie Formation of Dongying Sag in the Bohai Bay Basin, China. For these samples, the adsorbed amounts of C7H14 ranged from 18.03–28.02 mg/g (mean 23.33 mg/g, which is larger than that of C10H22, which ranges from 15.40–21.72 mg/g (mean 18.82 mg/g. The adsorption capacity of C7H8 was slightly low, ranging from 10.51–14.60 mg/g (mean 12.78 mg/g.

Fe(0)-clays interactions at 90°C under anoxic conditions: a comparative study between clay fraction of Callovo-Oxfordian and other purified clays

International Nuclear Information System (INIS)

Rivard, C.; Pelletier, M.; Villieras, F.; Barres, O.; Galmiche, M.; Ghanbaja, J.; Kohler, A.; Michau, N.

2010-01-01

Document available in extended abstract form only. In the context of the geological disposal of high-level radioactive waste it is of prime importance to understand the interactions between the saturated clay formation and steel containers. This can be achieved through an in-depth analysis of iron-clay interactions. Previous studies on the subject investigated the influence of solid/liquid ratio, iron/clay ratio, temperature and reaction time. The aim of the present study is to explain Callovo-Oxfordian-Fe(0) interactions by determining the role of each mineral phases present in the Callovo-Oxfordian (clay minerals, quartz, carbonates and pyrite) on the mechanisms of interaction between metal iron and clay particles. In that context, it is especially important to understand in detail the influence of clay nature and to obtain some insight about the relationships between interaction mechanisms at the molecular scale and crystallographic properties (particle size, TO or TOT layers, amount of edge faces...). The influence of the combination of different clays and the addition of other minerals must also be studied. In a first step, the Callovo-Oxfordian argillite from the Andra's underground research laboratory was purified to extract the clay fraction (illite, illite-smectite, kaolinite and chlorite). Batch experiments were carried out in anoxic conditions at 90 deg. C in the presence of background electrolyte (NaCl 0.02 M.L -1 , CaCl 2 0.04 M.L -1 ) for durations of one, three or nine months in the presence of metallic iron powder. Experiments without iron were used as control. The iron/clay ratio was fixed at 1/3 with a solid/liquid ratio of 1/20. The above mentioned experiments were also carried out in parallel on other purified clays: two smectites (Georgia bentonite and SWy2 from the Clay Minerals Society), one illite (illite du Puy) and one kaolinite (KGa2, from the Clay Minerals society). At the end of the experiments, solid and liquid phases were

Study of radionuclide migration in clay formations

International Nuclear Information System (INIS)

Antonioli, F.; Bocola, W.

1985-01-01

This paper reports the studies on the migration of Cs, Sr and I in clay formations, which are presently considered for the geological disposal of radioactive wastes. The distribution and diffusion coefficients were evaluated by means of experimental techniques and computer procedures, which are presented in this report. The natural clays tested in the laboratory experiments were sampled from the most representative italian basins and from the zone of Mol (Belgium). In addition tests were performed on monomineral clays artificially remade in edometer. The experimental results are in accordance with data found in the literature and show the existence of a good correlation between the observed migration properties and the granulometric and mineralogic characteristics of the natural clays

Clay mineral facies and lateritization in basalts of the southeastern Parana Basin, Brazil

International Nuclear Information System (INIS)

Oliveira, M.T.G. de; Formoso, M.L.L.; Trescases, J.J.; Meunier, A.

1998-01-01

Seventeen samples from two lateritic profiles, each with five facies, were studied. These profiles occur on the old planation surface of the plateau basalts of the southern part of ParanáBasin, Brazil. Optical microscopy, X-ray diffraction, electron microprobe, Mössbauer spectroscopy and Fourier Transform Infrared Spectra were used to obtain information about the nature and chemical composition of each weathering facies. In addition, scanning electron microscopy and analyses of clay minerals were performed to detect microcrystalline environmental changes. Both profiles have two major parts: a loose red-clay latosol separated from an underlying mottled clay and an alterite facies; a stone line may or may not be present between the latosol and the underlying units. In both profiles the latosol consists principally of kaolinite, hematite and goethite. Two alterite facies, shaped by differential weathering, are also present in the lower profile: a halloysite–nontronite clayey matrix with a well developed fissure system occurs in the argillaceous alterite and a network of Al–goethite aggregates is typical of the highly porous cortex of the boulder alterite that is found in the stone line and below it. Gibbsite has crystallized in the large pores of porphyritic boulder alterite but is absent in the small pores of the subaphyric boulder alterite. Clay minerals observed in fissures include halloysite associated with goethite and manganese oxides. The basalt has hydrothermal green-clays (mixed layers and trioctahedral smectites) that formed between primary plagioclase, pyroxene and Ti–magnetite crystals while fresh corestones of the boulder alterite have cryptocrystalline iron-rich material. The study of these profiles shows one principal evolutionary trend for clay minerals. This trend is from smectite and mixed layers that form green clays in altered bedrock at the base of the profile to an intermediate association of nontronite and halloysite in the argillaceous

Clay mineral distribution from Bhimunipatnam to Pudimadaka along cental eastern continental shelf of India

Digital Repository Service at National Institute of Oceanography (India)

Reddy, N.P.C.; Rao, K.M.

Forty eight sediment samples, collected from 50-100m depth, have been analysed for their clay mineral composition and distribution. Kaolinite with chlorite (K + C) is the predominant mineral followed by illite and montmorillonite. K + C and illite...

Use of thermogravimetry on rational analysis of clay minerals from state of Mato Grosso do Sul

International Nuclear Information System (INIS)

Salvetti, Alfredo Roque; Rodrigues, Henrique Mauro

1997-01-01

The rational analysis on clay minerals, normally uses as structural water, the mass loss by firing. The presence of organic materials, sulphur or others minerals, can cause an error on quantification of structural water. With the use of thermal gravimetric analysis, we can calculate, in a more precise way, the quantity of mass loss by dehydroxylation, without take into account the loss of mass from others process. We compared the rational chemical analysis on some clay minerals from state of Mato Grosso do Sul using burning loss and thermal gravimetric analysis. (author)

Origin of opal-ct in lower eocene tallahatta formation, mississippi, usa and pleistocene barind clay formation in bangladesh: A comparative study

International Nuclear Information System (INIS)

Kabir, S.

2008-01-01

Opal-CT mineral in the lower Eocene Tallahatta formation in Mississippi. USA and the Pleistocene Barind clay formation in Bangladesh is of volcanogenic origin. X-ray diffraction patterns of claystones in the former indicated more ordered condition on the older sediments than those of the latter, which may be due to higher burial temperatures and longer time interval for transformation from volcanic ash to opal-CT of the former. Glass shards, present in the latter sediments, were not identified in the former, which may be due to transformation of glass shards of volcanic ash to opal-Cr over the time. (author)

Effect of organic matter properties, clay mineral type and thermal maturity on gas adsorption in organic-rich shale systems

Science.gov (United States)

Zhang, Tongwei; Ellis, Geoffrey S.; Ruppel, Stephen C.; Milliken, Kitty; Lewan, Mike; Sun, Xun; Baez, Luis; Beeney, Ken; Sonnenberg, Steve

2013-01-01

A series of CH4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH4 molecules for sorption on organic matter

Comparative evaluation of clays from Abakaliki Formation with ...

African Journals Online (AJOL)

The characteristics of clays from Abakaliki Formation, Southeastern Nigeria was evaluated to establish its suitability as drilling mud when compared with commercial bentonite such as Wyoming bentonite. The chemical, mineralogical and geotechnical properties were employed in assessing the suitability of Abakaliki clay as ...

Effects of natural heating on a clay formation

International Nuclear Information System (INIS)

Polizzano, C.; Sensi, L.; Leoni, L.; Sartori, F.

1985-01-01

As a contribution to the characterization of clay deposits as possible sites for nuclear waste disposal, the metamorphic effects induced on Pliocene argillaceous sediments by the small subvolcanic body of Orciatico (Tuscany, Italy) were investigated. In areas close to marginal facies of the magmatic body, where temperatures were presumably ranging from 100 to 500 0 C, the thermo-metamorphic aureole thickness doesn't exceed 2 meters. In this zone the clay fraction (45-69% of the bulk rock) changes from an illite+illite/smectite interstratified+vermiculite+chloritic intergrades assemblage to a paragenesis characterized only by illite+smectite, the later being the most stable phase among the clay minerals. Within such zone alkalis (Na,K, and Rb) and alkaline-earths (Ca and Sr) result to be the most highly mobilized elements

The effect of high pH alkaline solutions on the mineral stability of the Boom Clay - Batch experiments at 60 deg. C

International Nuclear Information System (INIS)

Honty, M.; De Craen, M.; Wang, L.; Madejova, J.; Czimerova, A.; Pentrak, M.; Stricek, I.; Van Geet, M.

2010-01-01

Boom Clay is currently viewed as a reference host formation for studies on deep geological disposal of radioactive waste in Belgium. The interactions between bulk rock Boom Clay and 0.1 M KOH, 0.1 M NaOH, 0.1 M Ca(OH) 2 , young cement water and evolved cement water solutions, ranging in pH from 12.5 to 13.2, were examined as static batch experiments at 60 deg. C to simulate alkaline plume perturbations, which are expected to occur in the repository due to the presence of concrete. Both liquids and solids were investigated at specific times between 90 and 510 days in order to control the elemental budget and to search for potential mineralogical alterations. Also, the clay fraction was separated from the whole-rock Boom Clay at the end of each run and characterized for its mineralogical composition. Thereby, the importance of the mineral matrix to buffer the alkaline attack and the role of organic matter to protect clay minerals were also addressed. The results indicate that the degree of geochemical perturbation in Boom Clay is dependent on the initial pH of the applied solution together with the nature of the major cation in the reactant fluids. The higher the initial pH of the media, the stronger its interaction with Boom Clay. No major non-clay mineralogical alteration of the Boom Clay was detected, but dissolution of kaolinite, smectite and illite occurred within the studied experimental conditions. The dissolution of clays is accompanied by the decrease in the layer charge, followed by a decrease in the cation-exchange capacity. The highest TOC values coincide with the highest total elemental concentrations in the leachates, and correspondingly, the highest dissolution degree. However, no quantitative link could be established between the degree of organic matter decomposition and clay dissolution.

Repository tunnel construction in deep clay formations

International Nuclear Information System (INIS)

Clarke, B.G.; Mair, R.J.; Taylor, R.N.

1992-01-01

One of the objects of the Hades project at Mol, Belgium has been to evaluate the feasibility of construction of a deep repository in the Boom clay formation at depth of approximately 225 metres. The main objective of the present project was to analyse and interpret the detailed geotechnical measurements made around the Hades trial shaft and tunnel excavations and evaluate the safety of radioactive waste disposal in a repository facility in deep clay formations. Plasticity calculations and finite element analyses were used which gave results consistent with the in-situ measurements. It was shown that effective stress analysis could successfully predict the observed field behaviour. Correct modelling of the small-strain stiffness of the Boom clay was essential if reasonable predictions of the pore pressure response due to construction are to be made. The calculations undertaken indicated that, even in the long term, the pressures on the test drift tunnel lining are likely to be significantly lower than the overburden pressure. Larger long-term tunnel lining pressures are predicted for impermeable linings. A series of laboratory stress path tests was undertaken to determine the strength and stiffness characteristics of the Boom clay. The tests were conducted at appropriate effective stress levels on high-quality samples retrieved during construction of the test drift. The apparatus developed for the testing is described and the results discussed. The development of a self boring retracting pressure-meter is described. This novel in-situ testing device was specifically designed to determine from direct measurements the convergence/confinement curve relevant to tunnelling in clay formations. 44 refs., 60 figs., 3 tabs

Treatment and conditioning of radioactive waste solution by natural clay minerals

International Nuclear Information System (INIS)

El-Dessouky, M.I.; El-Massry, E.H.; Khalifa, S.M.; Aly, H.F.

1999-01-01

Natural inorganic exchangers. Was used to remove caesium, cobalt and europium using zinc sulfate as coagulant also different clay minerals. These calys include, feldrspare, aswanly, bentionite, hematite, mud, calcite, basalt, magnetite, kaoline sand stone, limonite and sand. The factros affecting the removal process namely PH, particle size, temperature and weight of the clay have been studied. Highest removal for Cs-137, Co-60 and Eu-152 and 154 was achived by asswanly and bentonite. Sand stone is more effective than the other clays. Removal of Cs-137 from low level waste solution is in the order the sequence, aswanly (85.5%)> bentonite (82.2%)> sandstone (65.4%). Solidified cement products have been evaluated to determine optimum conditions of mixing most sludges contained clays by testing mechanical strength and leaching rates of the waste products. The solidified waste forms were found more acceptable for handing, storage and ultimate disposal

Relationship between Mineral and Organic Matter in Shales: The Case of Shahejie Formation, Dongying Sag, China

Directory of Open Access Journals (Sweden)

Xiang Zeng

2018-05-01

Full Text Available Types of organic matter and mineral associations and microstructures of shales can reflect the depositional mechanism and sedimentary environment. Therefore, analysis of organic matter and mineral associations is a prerequisite for research on fine-grained sedimentary rocks. Shales from the Eocene Shahejie Formation in the Dongying Sag of China were selected to classify their lithofacies and to investigate the characteristics of their organic matter and mineral associations. This analysis identified six lithofacies (e.g., laminated shales and massive mudstones; in all the lithofacies, clay minerals exhibit a positive correlation with detrital minerals, thus indicating that they were derived from the same source. The comprehensive analysis of mineral and organic matter associations reveals that detrital minerals were deposited with low-hydrogen index (HI OM. The deposition of detrital minerals was mainly a physical process. Clay minerals can undergo deposition in one of two ways due to their surface charge: they can either aggregate with high-HI OM via chemical deposition, thus forming organic-rich laminae, or they can be deposited together with low-HI OM via physical deposition, thus forming clay-rich laminae or a massive matrix. Carbonate minerals, which often coexist with high-HI OM, are biological sediments. The analysis of the sedimentary characteristics of these organic matter and mineral associations indicates that the sedimentary processes differ between various lithofacies: e.g., the discontinuous laminated shale represents the product of biophysical processes. Differences in depositional mechanisms are also present in each sub-member. Therefore, it is important to analyze the properties of minerals and organic matter, as well as their associations, to more deeply understand the classification of lithofacies and the depositional processes of shales and mudstones.

Provenance and distribution of clay minerals in the sediments of the western continental shelf and slope of India

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P.; Rao, B.R.

-Goa (93 samples) For the convenience of description, the Saurashtra-Goa region has been divided into the Saurashtra, Gulf of Cambay-Ratnagiri and Ratnagiri-Goa sectors based on variations in clay mineral abundances. The boundaries between these sectors... are approximate and variations in the mineral abundances tend to grade one to the other. Smectite is the most abundant mineral in the inner shelf sediments of all the sectors [Fig. 3(Ba), 3(Ca) and Provenance and distribution of clay minerals 1763 0 Sm*ctlt* m...

Optimization method for quantitative calculation of clay minerals in soil

Indian Academy of Sciences (India)

However, no reliable method for quantitative analysis of clay minerals has been established so far. In this study, an attempt was made to propose an optimization method for the quantitative ... 2. Basic principles. The mineralogical constitution of soil is rather complex. ... K2O, MgO, and TFe as variables for the calculation.

Water-mineral interaction in hygromechanics of clays exposed to environmental loads

International Nuclear Information System (INIS)

Hueckel, T.A.

1992-01-01

Water-mineral interaction in narrow interstices (<3 nm) in dense, saturated clays is discussed in view of recent experimental findings and molecular dynamics simulations. Consequences to the macroscopic behavior are considered. A mixture theory for two interacting constituents is developed. Effects of temperature and chemicals are discussed. A postulate of mass transfer of absorbed water from solid to fluid fraction caused by thermal or chemical load is then discussed. Theory of plasticity of clays affected by heat or chemicals is developed to deal with the effects of thermal and chemical consolidation

Understanding the role of clay minerals in the chromium(VI) bioremoval by Pseudomonas aeruginosa CCTCC AB93066 under growth condition: microscopic, spectroscopic and kinetic analysis.

Science.gov (United States)

Kang, Chunxi; Wu, Pingxiao; Li, Yuewu; Ruan, Bo; Li, Liping; Tran, Lytuong; Zhu, Nengwu; Dang, Zhi

2015-11-01

Laboratory batch experiments were conducted to investigate the role of clay minerals, e.g., kaolinite and vermiculite, in microbial Cr(VI) reduction by Pseudomonas aeruginosa under growth condition in glucose-amended mediums as a method for treating Cr(VI)-contaminated subsurface environment such as soil. Our results indicated that glucose could acted as an essential electron donor, and clay minerals significantly enhanced microbial Cr(VI) reduction rates by improving the consumption rate of glucose and stimulating the growth and propagation of P. aeruginosa. Cr(VI) bioreduction by both free cells and clay minerals-amended cells followed the pseudo-first-order kinetic model, with the latter one fitting better. The mass balance analyses and X-ray photoelectron spectroscopy analysis found that Cr(VI) was reduced to Cr(III) and the adsorption of total chromium on clay minerals-bacteria complex was small, implying that Cr(VI) bioremoval was not mainly due to the adsorption of Cr(VI) onto cells or clay minerals or clay minerals-cells complex but mainly due to the Cr(VI) reduction capacity of P. aeruginosa under the experimental conditions studied (e.g., pH 7). Atomic force microscopy revealed that the addition of clay minerals (e.g. vermiculite) decreased the surface roughness of Cr(VI)-laden cells and changed the cell morphology and dimension. Fourier transform infrared spectroscopy revealed that organic matters such as aliphatic species and/or proteins played an important role in the combination of cells and clay minerals. Scanning electron microscopy confirmed the attachment of cells on the surface of clay minerals, indicating that clay minerals could provide a microenvironment to protect cells from Cr(VI) toxicity and serve as growth-supporting materials. These findings manifested the underlying influence of clay minerals on microbial reduction of Cr(VI) and gave an understanding of the interaction between pollutants, the environment and the biota.

Cathodoluminescence (CL) and electron paramagnetic resonance (EPR) studies of clay minerals

International Nuclear Information System (INIS)

Goetze, J.; Ploetze, M.; Goette, T.; Neuser, R.D.; Richter, D.K.

2002-01-01

Sheet silicates of the serpentine-kaolin-group (serpentine, kaolinite, dickite, nacrite, halloysite), the talc-pyrophyllite-group (talc, pyrophyllite), the smectite-group (montmorillonite), and illite (as a mineral of the mica-group) were investigated to obtain information concerning their cathodoluminescence behavior. The study included analyses by cathodoluminescence (CL microscopy and spectroscopy), electron paramagnetic resonance (EPR), x-ray diffraction (XRD), scanning electron microscopy (SEM) and trace element analysis. In general, all dioctahedral clay minerals exhibit a visible CL. Kaolinite, dickite, nacrite and pyrophyllite have a characteristic deep blue CL, whereas halloysite emission is in the greenish-blue region. On the contrary, the trioctahedral minerals (serpentine, talc) and illite do not show visible CL. The characteristic blue CL is caused by an intense emission band around 400 nm (double peak with two maxima at 375 and 410 nm). EPR measurements indicate that his blue emission can be related to radiation induced defect centers (RID), which occur as electron holes trapped on apical oxygen (Si-O center) or located at the Al-O-Al group (Al substituting Si in the tetrahedron). Additional CL emission bands were detected at 580 nm in halloysite and kaolinite, and between 700 and 800 nm in kaolinite, dickite, nacrite and pyrophyllite. Time-resolved spectral CL measurements show typical luminescence kinetics for the different clay minerals, which enable differentiation between the various dioctahedral minerals (e.g. kaolinite and dickite), even in thin section. (author)

Modified clay minerals efficiency against chemical and biological warfare agents for civil human protection.

Science.gov (United States)

Plachá, Daniela; Rosenbergová, Kateřina; Slabotínský, Jiří; Kutláková, Kateřina Mamulová; Studentová, Soňa; Martynková, Gražyna Simha

2014-04-30

Sorption efficiencies of modified montmorillonite and vermiculite of their mono ionic Na and organic HDTMA and HDP forms were studied against chemical and biological warfare agents such as yperite and selected bacterial strains. Yperite interactions with modified clay minerals were observed through its capture in low-density polyethylene foil-modified clay composites by measuring yperite gas permeation with using chemical indication and gas chromatography methods. The antibacterial activities of synthetized organoclays were tested against selected Gram-positive and Gram-negative bacterial species in minimum inhibitory concentration tests. The obtained results showed a positive influence of modified clay minerals on the significant yperite breakthrough-time increase. The most effective material was the polyethylene-Na form montmorillonite, while the polyethylene-Na form vermiculite showed the lowest efficiency. With increasing organic cations loading in the interlayer space the montmorillonite efficiency decreased, and in the case of vermiculite an opposite effect was observed. Generally the modified montmorillonites were more effective than modified vermiculites. The HDP cations seem to be more effective compare to the HDTMA. The antibacterial activity tests confirmed efficiency of all organically modified clay minerals against Gram-positive bacteria. The confirmation of antibacterial activity against Y. pestis, plague bacteria, is the most interesting result of this part of the study. Copyright © 2014 Elsevier B.V. All rights reserved.

Geochemical Investigation of Clay Minerals in Marte, Borno State, Nigeria

Directory of Open Access Journals (Sweden)

F. D. Adams

2017-10-01

Full Text Available Clay deposit collected from various locations in Marte (Northern Borno, were studied to determine their physical and chemical characteristics in order to evaluate their suitability for industrial uses. Major and trace element analyses were carried out on clay samples using Inductively Couple Plasma-Optical Emission Spectrometry (ICP-OES and X- Ray Fluorescence (XRF. The result of the chemical analysis of the ten (10 samples collected showed significant amounts of SiO2 and Al2O3. Silica content ranges from 51.48 to 62.44 % while alumina varies from 12.49 to 19.00 %. The calcium oxide ranges from 1.17 to 3.39 %, Na2O ranges from 1.1 to 8.61 %, K2O from 1.54 to 3.66 %, MgO varies from 0.04 to0.14 %, Fe2O3 varies from 0.3 to 2.7 % and MnO ranges from 0.01 to 1.03 %. The result showed that the clays are mainly smectite with quartz and felspar as the main non-clay minerals. Generally, the geochemical results of the samples do not meet the standard for industrial utilization when compared to the Industrial specifications. However, for industrial utilization, some of the clay samples may be used after necessary beneficiations.

THE STUDYING OF COLLOIDAL-CHEMICAL PROPERTIES OF CLAY MINERALS DISPERSIONS

Directory of Open Access Journals (Sweden)

A. F. Tymchuk

2015-02-01

Full Text Available The element structure is studied, the microscopic analysis of fine-dispersed min­eral systems (ground sediments of a mouth of the river Danube is carried out. The sedimentation process of clay minerals dispersions in solutions of surfactants and macromolecular substances is studied. Concentration intervals of stabilization of investigating dispersions were defined.

Assessment of Some Clay Deposits from Fatha Formation (M. Miocene for Brick Manufacturing in Koya Area, NE Iraq

Directory of Open Access Journals (Sweden)

Nawzat R. Ismail

2014-06-01

Full Text Available This paper deals with the evaluation of physical, chemical and mineralogical properties of claystone sediments of Miocene age (Fatha Formation and their suitability to use them as raw materials in manufacturing of building clay brick in Kurdistan (Koya city. The study based on the field reconnaissance for three sites of claystones which were selected from three different locations within Fatha Formation in Koya city, includes Haibat-Sultan area, Koya-Sulaimania road and central of Koya city. The clay samples were subjected to particle size distribution, chemical composition, mineralogical analysis, plasticity index and XRD tests. Clay tiles were produced by using Semi-dry method under load 78 kN/mm² and fired at 950 C°. The produced clay tiles were subjected to water absorption, efflorescence, shrinkage and compressive strength tests. The research has shown that the plasticity index depends on the mineral composition of the raw materials. The grain size analysis of raw materials, physical properties and mechanical properties of the produced tiles has shown the suitability of the used raw materials in producing class bricks of class A (first class according to the requirements of specification of the Iraqi Standard (1993.

Decontamination of radioactive liquid systems by modified clay minerals

OpenAIRE

Petrushka, Ihor; Moroz, Olexandr

2016-01-01

The process mechanism for sorption of strontium and cesium from liquid radioactive waste using modified bentonites from Yaziv sulfur deposit was investigated. The technique for predicting the intensity of the sorption process based on the comparison of experimental and calculated values of mass transfer coefficients was proposed. It was detected that the process of sorption extraction of strontium and cesium from liquid medium using modified clay minerals may be bes...

Stochastic Dynamics of Clay Translocation and Formation of Argillic Horizons

Science.gov (United States)

Calabrese, S.; Richter, D. D., Jr.; Porporato, A. M.

2017-12-01

The formation of argillic horizons in vertical soil profiles is mainly attributed to lessivage, namely the transport of clay from an upper E horizon to a deeper illuviated horizon. Because of the long timescales involved in this phenomenon, quantitative modeling is useful to explore the role of clay lessivage on soil formation and sub-surface clay accumulation. The limitations of detailed models of colloidal transport to short timescales make it necessary to resort to simple models. Here, we present a parsimonious model of clay transport in which lessivage is interpreted stochastically. Clay particles approach the soil surface at a speed equal to the erosion rate and are intermittently transported to deeper soil layers when percolation events occur or removed by erosion. Along with the evolution of clay particles trajectories, the model predicts the vertical clay profile, the depth of the B horizon, and the mean time to erosion. Dimensional analysis reveals the two dimensionless parameters governing the dynamics, leading to a new classification of soil types based on erosion rates and intensity of lessivage.

Radiostratigraphy and heavy mineral content of the Weches Formation (Eocene), Nacogdoches County, Texas

International Nuclear Information System (INIS)

Jobe, K.; Ledger, E.B.; Sharp, P.; Crocker, M.C.

1993-01-01

The Weches Formation of eastern Texas is a mudstone containing green sand-size clay aggregates. A vertical sequence of 43 samples was analyzed along an excavated cliff to determine radionuclide content. Samples average 5 ppm uranium and range from 2 to about 7 ppm. Thorium averages 20 ppm and ranges from 13 to almost 36 ppm. the gamma-ray spectrometer employed exhibits a certainty of about ±10% (one standard deviation) at the levels measured. Heavy mineral studies of mudstones are few, so one sample of the Weches mudstone was selected for heavy mineral separation and point counting of grain mounts. A total of 2606 grains were counted giving mineral percentages of zircon (28.8%), garnet (17.9%), tourmaline (10.5%), titanite (8.7%), apatite (7.6%), staurolite (6.4%), green hornblende (5.2%), epidote (5.1%), sillimanite (2.8%), monatite (2.2%), kyanite (1.9%), basaltic hornblende (1.5%), and biotite (1.3%). In addition, actinolite, spinel, rutile, and collophane were observed but not counted. Previous studies found a similar heavy mineral suite in the underlying Queen City Formation, but in different proportions. Differences in heavy mineral percentages probably reflect different water-flow regimes at the time of deposition. Heavy minerals in the Weches and Queen City formations are from the same general source area Measured radionuclide ratios are similar to granitic ratios and suggest that detrital heavy minerals, particularly zircon and monazite, are the main site of uranium and thorium and their decay products in the Weches Formation

Selenium containing clays minerals as additive for the discoloration of glass

NARCIS (Netherlands)

Timmer, K.; Limpt, J.A.C. van; Fischer, H.R.

2010-01-01

While selenium is applied as decolorizing agent for flint container glass or tableware glass, the retention of selenium in glass however is very low. Generally more than 75% of the total selenium input sublimes from the glass melt and leaves the clay minerals due to the high volatility of

Surface clay formation during short-term warmer and wetter conditions on a largely cold ancient Mars

Science.gov (United States)

Bishop, Janice L.; Fairén, Alberto G.; Michalski, Joseph R.; Gago-Duport, Luis; Baker, Leslie L.; Velbel, Michael A.; Gross, Christoph; Rampe, Elizabeth B.

2018-03-01

The ancient rock record for Mars has long been at odds with climate modelling. The presence of valley networks, dendritic channels and deltas on ancient terrains points towards running water and fluvial erosion on early Mars1, but climate modelling indicates that long-term warm conditions were not sustainable2. Widespread phyllosilicates and other aqueous minerals on the Martian surface3-6 provide additional evidence that an early wet Martian climate resulted in surface weathering. Some of these phyllosilicates formed in subsurface crustal environments5, with no association with the Martian climate, while other phyllosilicate-rich outcrops exhibit layered morphologies and broad stratigraphies7 consistent with surface formation. Here, we develop a new geochemical model for early Mars to explain the formation of these clay-bearing rocks in warm and wet surface locations. We propose that sporadic, short-term warm and wet environments during a generally cold early Mars enabled phyllosilicate formation without requiring long-term warm and wet conditions. We conclude that Mg-rich clay-bearing rocks with lateral variations in mixed Fe/Mg smectite, chlorite, talc, serpentine and zeolite occurrences formed in subsurface hydrothermal environments, whereas dioctahedral (Al/Fe3+-rich) smectite and widespread vertical horizonation of Fe/Mg smectites, clay assemblages and sulphates formed in variable aqueous environments on the surface of Mars. Our model for aluminosilicate formation on Mars is consistent with the observed geological features, diversity of aqueous mineralogies in ancient surface rocks and state-of-the-art palaeoclimate scenarios.

Sedimentological and clay mineral studies in Kakinada Bay, east coast of India

Digital Repository Service at National Institute of Oceanography (India)

Reddy, N.P.C.; Rao, K.M.

are of sandy sediments (2.9 to 3.05 phi). Interrelationships of size statistical parameters and the CM diagram of the bay sediments suggest a mechanism of slow deposition from quiet water. Montmorillonite is the predominant clay mineral followed by kaolinite...

Radiolysis of alanine adsorbed in a clay mineral

Energy Technology Data Exchange (ETDEWEB)

Aguilar-Ovando, Ellen Y.; Negron-Mendoza, Alicia [Instituto de Ciencias Nucleares, Universidad Nacional Autonoma de Mexico (UNAM), Circuito Exterior s/n, Ciudad Universitaria, Apartado Postal 70-543, Deleg. Coyoacan, C.P. 04510 (Mexico)

2013-07-03

Optical activity in molecules is a chemical characteristic of living beings. In this work, we examine the hypothesis of the influence of different mineral surfaces on the development of a specific chirality in organic molecules when subjected to conditions simulating the primitive Earth during the period of chemical evolution. By using X-ray diffraction techniques and HPLC/ELSD to analyze aqueous suspensions of amino acids adsorbed on minerals irradiated in different doses with a cobalt-60 gamma source, the experiments attempt to prove the hypothesis that some solid surfaces (like clays and meteorite rocks) may have a concentration capacity and protective role against external sources of ionizing radiation (specifically {gamma}-ray) for some organic compounds (like some amino acids) adsorbed on them. Preliminary results show a slight difference in the adsorption and radiolysis of the D-and L-alanine.

Radiolysis of alanine adsorbed in a clay mineral

International Nuclear Information System (INIS)

Aguilar-Ovando, Ellen Y.; Negrón-Mendoza, Alicia

2013-01-01

Optical activity in molecules is a chemical characteristic of living beings. In this work, we examine the hypothesis of the influence of different mineral surfaces on the development of a specific chirality in organic molecules when subjected to conditions simulating the primitive Earth during the period of chemical evolution. By using X-ray diffraction techniques and HPLC/ELSD to analyze aqueous suspensions of amino acids adsorbed on minerals irradiated in different doses with a cobalt-60 gamma source, the experiments attempt to prove the hypothesis that some solid surfaces (like clays and meteorite rocks) may have a concentration capacity and protective role against external sources of ionizing radiation (specifically γ-ray) for some organic compounds (like some amino acids) adsorbed on them. Preliminary results show a slight difference in the adsorption and radiolysis of the D-and L-alanine

Burial history of two potential clay host formations in Belgium

International Nuclear Information System (INIS)

Mertens, J.; Wouters, L.; Van Marcke, Ph.

2004-01-01

When dealing with long term stability of repository host rocks, it is important to consider and learn from all past geological events since the deposition of the formations. The burial history of the Boom Clay and Ypresian Clays, both considered as potential host rocks in Belgium, illustrates that the North Belgian region was tectonically relatively stable since deposition. In Northern Belgium, where both formations are located at a few hundreds meters of depth, tectonic movements were relatively small and no significant uplifts took place. The burial history of the Boom Clay in Mol, where the HADES underground research facility is located illustrates this. On the poster, the burial history for both formations is presented at two locations each: one location in the outcrop region and one research site location, where the formation is currently buried under a few 100 metres of sediment. (authors)

Sodium-calcium ion exchange on clay minerals at moderate to high ionic strengths

International Nuclear Information System (INIS)

Rogers, W.J.

1979-12-01

Sodium-calcium ion exchange on several clay minerals was studied at ionic strengths ranging from 0.01 to above 1.0. The minerals studied included attapulgite, illite, kaolin, and several montmorillonites. Distribution coefficients of calcium and sodium were obtained for the minerals over a wide range of solution conditions at pH five and equilibrium constants were calculated. The distribution coefficient of calcium, D/sub Ca/, was studied as a function of time, solution pH, loading, sodium concentration, and ionic strength fraction of sodium in constant ionic strength solutions. The distribution coefficient of sodium, D/sub Na/, was also studied as a function of time, loading, and sodium ionic strength fraction in constant total ionic strength solutions. Values of equilibrium constants calculated from distribution coefficients for solutions of constant ionic strength scattered bwteen 2 and 10 kg/kg for the montmorillonites and attapulgite while equilibrium constants for illite ranged from 5 to 10 kg/kg. No equilibrium constants for kaolin were calculated since distribution coefficients of sodium on this clay were too small to be measured. It was found that equilibrium constants at trace sodium loading were generally lower than those for higher sodium loadings by an order of magnitude or more due to the sensitivity of sodium distribution coefficients to the concentration of sodium in the clay at low loadings. Theoretical and experimental treatments of ion exclusion were included

Geothermal alteration of clay minerals and shales: diagenesis

Energy Technology Data Exchange (ETDEWEB)

Weaver, C.E.

1979-07-01

The objective of this report is to perform a critical review of the data on the mineral and chemical alterations that occur during diagenesis and low-grade metamorphism of shale and other clay-rich rocks - conditions similar to those expected from emplacement of heat-producing radioactive waste in a geologic repository. The conclusions drawn in this document are that the following type of alterations could occur: smectite alteration, ion mobilization, illitic shales, kaolinite reactions, chlorite reactions, organic reactions, paleotemperatures, low temperature shales, high temperature shales, and phase equilibrium changes.

Geothermal alteration of clay minerals and shales: diagenesis

International Nuclear Information System (INIS)

Weaver, C.E.

1979-07-01

The objective of this report is to perform a critical review of the data on the mineral and chemical alterations that occur during diagenesis and low-grade metamorphism of shale and other clay-rich rocks - conditions similar to those expected from emplacement of heat-producing radioactive waste in a geologic repository. The conclusions drawn in this document are that the following type of alterations could occur: smectite alteration, ion mobilization, illitic shales, kaolinite reactions, chlorite reactions, organic reactions, paleotemperatures, low temperature shales, high temperature shales, and phase equilibrium changes

Application of short-wave infrared (SWIR) spectroscopy in quantitative estimation of clay mineral contents

International Nuclear Information System (INIS)

You, Jinfeng; Xing, Lixin; Pan, Jun; Meng, Tao; Liang, Liheng

2014-01-01

Clay minerals are significant constituents of soil which are necessary for life. This paper studied three types of clay minerals, kaolinite, illite, and montmorillonite, for they are not only the most common soil forming materials, but also important indicators of soil expansion and shrinkage potential. These clay minerals showed diagnostic absorption bands resulting from vibrations of hydroxyl groups and structural water molecules in the SWIR wavelength region. The short-wave infrared reflectance spectra of the soil was obtained from a Portable Near Infrared Spectrometer (PNIS, spectrum range: 1300∼2500 nm, interval: 2 nm). Due to the simplicity, quickness, and the non-destructiveness analysis, SWIR spectroscopy has been widely used in geological prospecting, chemical engineering and many other fields. The aim of this study was to use multiple linear regression (MLR) and partial least squares (PLS) regression to establish the optimizing quantitative estimation models of the kaolinite, illite and montmorillonite contents from soil reflectance spectra. Here, the soil reflectance spectra mainly refers to the spectral reflectivity of soil (SRS) corresponding to the absorption-band position (AP) of kaolinite, illite, and montmorillonite representative spectra from USGS spectral library, the SRS corresponding to the AP of soil spectral and soil overall spectrum reflectance values. The optimal estimation models of three kinds of clay mineral contents showed that the retrieval accuracy was satisfactory (Kaolinite content: a Root Mean Square Error of Calibration (RMSEC) of 1.671 with a coefficient of determination (R 2 ) of 0.791; Illite content: a RMSEC of 1.126 with a R 2 of 0.616; Montmorillonite content: a RMSEC of 1.814 with a R 2 of 0.707). Thus, the reflectance spectra of soil obtained form PNIS could be used for quantitative estimation of kaolinite, illite and montmorillonite contents in soil

Climatic control on clay mineral formation: Evidence from ...

Indian Academy of Sciences (India)

are the most important factors that determine kinetics of chemical weathering. Mineral alteration ... perature, pressure and microbial activity. Among various factors ... physical factor) and rainfall (a chemical factor). (Velde 1992, p. 118).

X-ray diffraction identification of clay minerals by microcomputer

International Nuclear Information System (INIS)

Rodrigues, S.; Imasava, F.J.

1988-01-01

The identification of clay minerals by X-ray powder diffraction are done by searching an unknown pattern with a file of standard X-ray diffraction patterns. For this searching done by hand is necessary a long time. This paper shows a program in ''Basic'' language to be utilized in microcomputers for the math of the unknown pattern, using the high velocity of comparison of the microcomputer. A few minutes are used for the match. (author) [pt

The role of clay minerals in the preservation of organic matter in sediments of Qinghai Lake, NW China

Science.gov (United States)

Yu, Bingsong; Dong, Hailiang; Jiang, Hongchen; Lv, Guo; Eberl, Dennis D.; Li, Shanying; Kim, Jinwook

2009-01-01

The role of saline lake sediments in preserving organic matter has long been recognized. In order to further understand the preservation mechanisms, the role of clay minerals was studied. Three sediment cores, 25, 57, and 500 cm long, were collected from Qinghai Lake, NW China, and dissected into multiple subsamples. Multiple techniques were employed, including density fractionation, X-ray diffraction, scanning and transmission electron microscopy (SEM and TEM), total organic carbon (TOC) and carbon compound analyses, and surface area determination. The sediments were oxic near the water-sediment interface, but became anoxic at depth. The clay mineral content was as much as 36.8%, consisting mostly of illite, chlorite, and halloysite. The TEM observations revealed that organic matter occurred primarily as organic matter-clay mineral aggregates. The TOC and clay mineral abundances are greatest in the mid-density fraction, with a positive correlation between the TOC and mineral surface area. The TOC of the bulk sediments ranges from 1 to 3% with the non-hydrocarbon fraction being predominant, followed by bitumen, saturated hydrocarbon, aromatic hydrocarbons, and chloroform-soluble bitumen. The bimodal distribution of carbon compounds of the saturated hydrocarbon fraction suggests that organic matter in the sediments was derived from two sources: terrestrial plants and microorganisms/algae. Depthrelated systematic changes in the distribution patterns of the carbon compounds suggest that the oxidizing conditions and microbial abundance near the water-sediment interface promote degradation of labile organic matter, probably in adsorbed form. The reducing conditions and small microbial biomass deeper in the sediments favor preservation of organic matter, because of the less labile nature of organic matter, probably occurring within clay mineral-organic matter aggregates that are inaccessible to microorganisms. These results have important implications for our

Possibilities for the storage of radioactive waste in deep clay formations

International Nuclear Information System (INIS)

Le Pochat, G.; Lienhardt, M.J.; Peaudecerf, P.; Platel, J.P.; Simon, J.M.; Berest, P.; Charpentier, J.P.; Andre-Jehan, R.

1984-02-01

The possible storage sites in deep clay formations have been studied in parts of large French sedimentary basins which prima facie seem to have suitable characteristics. The most suitable areas were chosen on the basis of earlier oil prospecting data consisting of information on seismic movements, diagraphic well-logging data and old samples that happened to have been preserved. At the same time, the lithology of the clay formations can be determined from mineralogical studies on samples taken from boreholes or from outcrops. Before carrying out in situ experiments concerned with the geotechnical characterization of the deep clays, measurements were made in the laboratory on samples obtained in two ways: from tertiary clay outcrops and from cores taken at 950 m in the clay layers during oil well logging. The results of studies carried out on tertiary clays in Les Landes illustrate this procedure

Formation mechanism of uranium minerals at sandstone-type uranium deposits

International Nuclear Information System (INIS)

Li Shengfu; Zhang Yun

2004-01-01

By analyzing the behavior and existence form of uranium in different geochemical environments, existence form of uranium and uranium minerals species, this paper expounds the formation mechanism of main commercial uranium mineral--pitchblende: (1) uranium is a valence-changeable element. It is reactivated and migrates in oxidized environment, and is reduced and precipitated in reducing environment; (2) [UO 2 (CO 3 ) 3 ] 4- , [UO 2 (CO 3 ) 2 ] 2- coming from oxidized environment react with reductants such as organic matter, sulfide and low-valence iron at the redox front to form simple uranium oxide--pitchblende; (3)the adsorption of uranium by organic matter and clay minerals accelerates the reduction and the concentration of uranium. Therefore, it is considered, that the reduction of SO 4 2- by organic matter to form H 2 S, and the reduction of UO 2 2+ by H 2 S are the main reasons for the formation of pitchblende. This reaction is extensively and universally available in neutral and weakly alkaline carbonate solution. The existense of reductants such as H 2 S is the basic factor leading to the decrease of Eh in environments and the oversaturation of UO 2 2+ at the redox front in groundwater, thus accelerating the adsorption and the precipitation of uranium

Multi-scale experimental and numerical study of the structure and the dynamics of water confined in clay minerals

International Nuclear Information System (INIS)

Guillaud, Emmanuel Bertrand

2017-01-01

Clay are complex minerals with a multi-scale porosity and a remarkable ability to swell under humid atmosphere. These materials have many applications in catalysis, waste management, construction industry... However, the properties of confined water are still not fully understood, due in particular to the complexity of water itself. The aim of this work is, using mainly molecular simulations and vibrational spectroscopy, to understand the structure and the dynamics of water confined in clay minerals. To evaluate the accuracy of numerical models to describe water confined in clay minerals, and to understand the origin of its structural and dynamical properties, a large part of the work was devoted to the building blocks of clays: pure bulk water, water at the surface of a solid, and salt water. To this extent, the viscoelastic properties of water from the deeply supercooled regime to the boiling temperature were investigated using classical molecular dynamics. The evolution of the friction properties of water on a prototypical solid surface was also analyzed, and the accuracy of ab initio approaches and empirical salt models was studied. In a second part, those results were confronted to the properties of water confined in clay minerals at low and room temperature, studied both experimentally and numerically. Experimental work consisted mostly in extensive far- and -mid infrared absorption spectrometry measurements, whereas numerical work mainly consisted in empirical molecular dynamics simulations. Especially, the existence of confinement- or temperature-induced phase transitions of confined water was investigated. (author)

Pure and impure clays and their firing products

International Nuclear Information System (INIS)

Murad, E.; Wagner, U.

1989-01-01

Moessbauer spectroscopy is highly suited for the study of clays whose industrial uses depend on the iron content. Reactions that take place during clay firing can be readily monitored by Moessbauer spectroscopy. Following dehydroxylation of clay minerals, the quadrupole splitting of octahedrally coordinated iron (III) increases abruptly, but reverts to lower values upon the formation of new, better ordered phases at higher temperatures. It is also shown that iron oxides may account for a considerably higher proportion of the total iron content of many clays than is commonly recognized, and their existence must be taken into consideration for a correct interpretation of the Moessbauer spectra of clays. (orig.)

Redox properties of clay-rich sediments as assessed by mediated electrochemical analysis : Separating pyrite, siderite and structural Fe in clay minerals

NARCIS (Netherlands)

Hoving, Alwina L.; Sander, Michael; Bruggeman, Christophe; Behrends, Thilo

2017-01-01

Redox reactions with Fe-containing minerals in clay-rich sediments largely affect the speciation, mobility, and (bio-) availability of redox-sensitive contaminants. Here, we use mediated electrochemical oxidation (MEO) and reduction (MER), to quantify the electron accepting and donating capacities

Spatial distribution and longitudinal variation of clay minerals in the Central Indian Basin

Digital Repository Service at National Institute of Oceanography (India)

Valsangkar, A.

in the Central Indian Basin (CIB). The average sand content in the basin is 3.8%, which decreases systematically and longitudinally to 0.3% towards south. The average illite and chlorite major clay mineral abundance also decrease southwards along the four...

Heterogeneous uptake of the C1 to C4 organic acids on a swelling clay mineral

Directory of Open Access Journals (Sweden)

M. A. Tolbert

2007-08-01

Full Text Available Mineral aerosol is of interest due to its physiochemical impacts on the Earth's atmosphere. However, adsorbed organics could influence the chemical and physical properties of atmospheric mineral particles and alter their impact on the biosphere and climate. In this work, the heterogeneous uptake of a series of small organic acids on the swelling clay, Na-montmorillonite, was studied at 212 K as a function of relative humidity (RH, organic acid pressure and clay mass. A high vacuum chamber equipped with a quadrupole mass spectrometer and a transmission Fourier transform infrared spectrometer was used to detect the gas and condensed phases, respectively. Our results show that while the initial uptake efficiency was found to be independent of organic acid pressure, it increased linearly with increasing clay mass. Thus, the small masses studied allow access to the entire surface area of the clay sample with minimal effects due to surface saturation. Additionally, results from this study show that the initial uptake efficiency for butanoic (butyric acid on the clay increases by an order of magnitude as the RH is raised from 0% to 45% RH at 212 K while the initial uptake efficiency of formic, acetic and propanoic (propionic acids increases only slightly at higher humidities. However, the initial uptake efficiency decreases significantly in a short amount of time due to surface saturation effects. Thus, although the initial uptake efficiencies are appropriate for initial times, the fact that the uptake efficiency will decrease over time as the surface saturates should be considered in atmospheric models. Surface saturation results in sub-monolayer coverage of organic acid on montmorillonite under dry conditions and relevant organic acid pressures that increases with increasing humidity for all organic acids studied. Additionally, the presence of large organic acids may slightly enhance the water content of the clay above 45% RH. Our results indicate

Physical Properties of Latvian Clays

OpenAIRE

Jurgelāne, I; Stepanova, V; Ločs, J; Mālers, J; Bērziņa-Cimdiņa, L

2012-01-01

Physical and chemical properties of clays mostly depends on its mineral and chemical composition, particle size and pH value. The mutual influence of these parameters is complex. Illite is the most abundant clay mineral in Latvia and usually used in building materials and pottery. The viscosity and plasticity of Latvian clays from several deposits were investigated and correlated with mineral composition, particle size and pH value. Fractionated and crude clay samples were used. The p...

Studies on Tagged Clay Migration Due to Water Movement

International Nuclear Information System (INIS)

Scharpenseel, H.W.; Kerpen, W.

1967-01-01

55 Fe-tagged clay minerals, produced by hydrothermal synthesis, serve to clarify the question whether clay migration or clay formation in situ is the predominating mechanism in the B t -development of Parabraunerde (sol brun lessive, grey brown podsolic, hapludalf, dernopodsol). They further indicate the possibilities of clay transportation caused by water percolation. Suitable experimental approaches, such as thin-layer chromatography and autoradiography, translocation tests in columns filled with monotypical textural fractions or with undisturbed soil profiles, and synchronous hydrothermal treatment of 55 Fe-con raining material from different horizons of Parabraunerde, to reveal the specific readiness of the different profile zones for 55 Fe-clay production, are described. The possibilities of clay percolation are discussed. (author)

Sorption kinetics and chemical forms of Cd(II) sorbed by thiol-functionalized 2:1 clay minerals

International Nuclear Information System (INIS)

Malferrari, D.; Brigatti, M.F.; Laurora, A.; Pini, S.; Medici, L.

2007-01-01

The interaction between Cd(II) in aqueous solution and two 2:1 expandable clay minerals (i.e., montmorillonite and vermiculite), showing different layer charge, was addressed via batch sorption experiments on powdered clay minerals both untreated and amino acid (cysteine) treated. Reaction products were characterized via X-ray powder diffraction (XRDP), chemical analysis (elemental analysis and atomic absorption spectrophotometry), thermal analysis combined with evolved gasses mass spectrometry (TGA-MSEGA) and synchrotron-based X-ray absorption spectroscopy via extended X-ray absorption fine structure (EXAFS) characterization. Sorption isotherms for Cd(II) in presence of different substrates, shows that Cd(II) uptake depends both on Cd(II) starting concentration and the nature of the substrate. Thermal decomposition of Cd-cysteine treated clay minerals evidences the evolution of H 2 O, H 2 S, NO 2 , SO 2 , and N 2 O 3 . These results are well consistent with XRDP data collected both at room and at increasing temperature and further stress the influence of the substrate, in particular cysteine, on the interlayer. EXAFS studies suggest that Cd(II) coordinates with oxygen atoms, to give monomer complexes or CdO molecules, either on the mineral surface and/or in the interlayer. For Cd-cysteine complexes EXAFS data agree with the existence of Cd-S clusters, thus suggesting a predominant role of the thiol group in the bonding of Cd with the amino acid

Viscosity and Plasticity of Latvian Illite Clays

OpenAIRE

Jurgelāne, I; Vecstaudža, J; Stepanova, V; Mālers, J; Bērziņa-Cimdiņa, L

2012-01-01

Due to viscosity and plasticity, clays and clay minerals are used in civil engineering, pottery and also in cosmetics and medicine as thickening agents and emulsion and suspension stabilizers. The rheological properties of clay suspensions are complex. Mostly it is an interaction between mineral composition, clay particle size and pH value and also depends on clay minerals. Clay-water suspension is non-Newtonian fluid showing thixotropic and pseudoplastic properties. Results showed that plast...

Clay minerals in uraniferous deposit of Imouraren (Tim Mersoi basin, Niger): implications on genesis of deposit and on ore treatment process

International Nuclear Information System (INIS)

Billon, Sophie

2014-01-01

Nigerian uraniferous deposits are located in carboniferous and Jurassic formations of Tim Mersoi basin. AREVA is shareholder of 3 mine sites in this area: SOMAIR and COMINAK, both in exploitation since 1960's and IMOURAREN, 80 km further South, whose exploitation is planned for 2015. Mineralization of Imouraren deposit is included in the fluvial formation of Tchirezrine 2 (Jurassic), composed of channels and flood plains. Facies of channel in-fillings range from coarse sandstones to siltstones, while overflow facies are composed of analcimolites. Secondary mineralogy was acquired during 2 stages: 1- diagenesis, with formation of clay minerals, analcime, secondary quartz and albites, and 2- stage of fluids circulations, which induced alteration of detrital and diagenetic minerals, formation of new phases and uranium deposition. A mineralogical zoning, at the scale of deposit resulted from this alteration. The heterogeneity of Tchirezrine 2, at the level of both facies and mineralogy, is also evidenced during ore treatment, as ore reacts differently depending on its source, with sometimes problems of U recovery. Ore treatment tests showed that analcimes and chlorites were both penalizing minerals, because of 1- the sequestration of U-bearing minerals into analcimes, 2- their dissolution which trends to move away from U solubilization conditions (pH and Eh) and to form numerous sulfates, and 3- problems of percolation. A detection method of analcime-rich ores, based on infrared spectroscopy, was developed in order to optimize ore blending and so to reduce negative effects during ore treatment process. (author)

Early-middle Eocene birds from the Lillebaelt Clay Formation of Denmark

DEFF Research Database (Denmark)

Lindow, Bent Erik Kramer

2009-01-01

The marine Lillebaelt Clay Formation of central Denmark is of early-middle Eocene age (late Ypresian - middle Lutetian; microfossil zones NP 13-NP 15). Over 20 bird fossils collected by amateur palaeontologists have been acquired through the Danish national ‘Danekrae' fossil treasure trove...... Clay Formation deposits derive from just after the Early Eocene Climate Optimum, a period of global elevated temperatures resulting from rapid greenhouse warming. Comparison between this bird assemblage and the recently revised assemblage from the older (earliest Ypresian) Fur Formation of Denmark...

Treatment and Conditioning of Radioactive Waste Solution by Natural Clay Minerals

International Nuclear Information System (INIS)

El-Dessouky, M.I.; Abdel-Raouf, M.W.; El-Massry, E.H.; Khalifa, S.M.; Aly, H.F.

1999-01-01

Chemical precipitation processes have been used for the treatment of radioactive elements from aqueous solution. The volume reduction is not very great and storage facilities are expensive. There are some radionuclides which are so difficult to be precipitated by this common method, so they may be precipitated by adding solid materials such as natural inorganic exchangers. In this woek, improvement the removal of caesium, cobalt and europium with zinc sulfate as coagulant and different clay minerals have been investigated. These include, Feldespare, Aswanly, Bentionite, Hematite, Mud, Calcite, Basalt, Magnetite, Kaoline, Sand stone, Limonite and Sand. The parameters affecting the precipitation process such as pH, particle size, temperature and weight of the clay have been studied. The results indicate that, the highest removal for Cs-137, Co-60 and Eu-152 and154 by Asswanly, Bentonite and Sand stone is more than the other clays. Removal of Cs-137 from low level waste solution with these three natural clays took the sequence, Aswanly (85.5%) > Bentonite (82.2%) > Sandstone (65.4%). Solidified cement products have been evaluated to determine mechanical strength and leaching rates of the waste products. The solidified waste forms were found more acceptable for handling ,storage and ultimate disposal

Competitive sorption between glyphosphate and inorganic phosphate on clay minerals and low organic matter soils

International Nuclear Information System (INIS)

Dion, H.M.; Hill, H.H.Jr.; Washington State Univ., Pullmann, WA; Harsh, J.B.; Washington State Univ., Pullmann, WA

2001-01-01

Inorganic phosphate may influence the adsorption of glyphosate to soil surface sites. It has been postulated that glyphosphate sorption is dominated by the phosphoric acid moiety, therefore, inorganic phosphate could compete with glyphosate for surface sorption sites. Sorption of glyphosate is examined in low organic carbon systems where clay minerals dominate the available adsorption sites using 32 P-labeled phosphate and 14 C-labeled glyphosate to track sorption. Glyphosate sorption was found to be strongly dependent on phosphate additions. Isotherms were generally of the L type, which is consistent with a limited number of surface sites. Most sorption on whole soils could be accounted for by sorption observed on model clays of the same mineral type as found in the soils. (author)

Synthesis and characterization of carbon nanotubes on clay minerals and its application to a hydrogen peroxide biosensor

International Nuclear Information System (INIS)

Hsu, H.-L.; Jehng, J.-M.

2009-01-01

In this study, we demonstrate the synthesis of carbon nanotubes (CNTs) on clay minerals, and the development of biosensors based on Nafion-CNT/Clay-Au and Nafion-CNT/Clay-Au-Glucose oxidase (GOD) composite films for the detection of hydrogen peroxide (H 2 O 2 ) and glucose, respectively. The CNTs are synthesized on nickel cation exchanged clay mineral platelets. From field-emission scanning electron microscope images, X-ray diffraction, Fourier transfer infrared and thermogravimetric analysis results, the clay layers are exfoliated and delaminated after the growth of CNTs on them. The mixed hybrid film of Nafion, CNT/Clay, Au particles and GOD is coated on the glassy carbon (GC) electrode to detect H 2 O 2 or glucose. This film exhibits a detection limit of 5.0 x 10 -5 M for H 2 O 2 with a sensitivity of 280 nA mM -1 . In addition, the amperometric response for glucose containing 2.0 mg mL -1 GOD in the Nafion-CNT/Clay-Au-GOD modified GC electrode exhibits a sensitivity of 620 nA mM -1 with a linear range up to 1850 μM. A higher sensitivity and shorter response time are observed with increasing GOD content in the composite matrix film. Besides, the highest sensitivity of 2032 nA mM -1 is obtained with the addition of the 10.0 mg mL -1 GOD in the composite film. Consequently, the CNT/Clay/Nafion medium can probably be a useful electrode for the development of sensors due to its high sensitivity and applicability

Preferred Orientation and Anisotropy of Clay minerals and Pores in Posidonia Shales

Science.gov (United States)

Kanitpanyacharoen, W.; Chen, K.; Wenk, H.

2010-12-01

Shales compose a large part of sedimentary basins and form the seal and source rocks for hydrocarbon reservoirs. They are also of great interest in context of repositories for nuclear waste and carbon sequestration. A comprehensive study of shale properties is thus crucial for seismic prospecting, particularly due to high elastic anisotropy that is contributed by the alignment of constituent clay minerals during compaction and diagenesis. In this study, we quantitatively analyze composition, crystal preferred orientation (or texture), and the 3D porosity structure in four Posidonia shales from Germany using high energy synchrotron x-rays. We can infer texture information from x-ray diffraction images relying on the Rietveld method, as well as determine the 3D porosity structure from tomography images. We observed that quartz and calcite are dominating phases while illite-smectite, illite-mica and kaolinite are the major clay minerals. The texture strength of clays range from 4.22 to 6.12 m.r.d. A comparison of shallow Posidonia shales with deep shales from the North Sea, Saudi Arabia, and the Gulf of Mexico documents that P-wave anisotropy increases with increasing phyllosilicate content (mainly illite-smectite and kaolinite) and increasing burial. Low absorption features in microtomography images indicate porosity (including kerogen and fractures), which is estimated at 1 vol% and observed to be anisotropic, mainly organized parallel to bedding with little connectivity of flat pores in direction perpendicular to the bedding plane.

Rare earth elements distribution in clay zones of sedimentary formation, Pondicherry, south India

International Nuclear Information System (INIS)

Tirumalesh, K.; Gursharan Singh

2012-01-01

Concentrations of five rare earth elements (REE) were measured in clay samples of a deep bore hole comprising major aquifers of Pondicherry region, south India in order to investigate the geochemical variations among various litho-units. Clay samples from Cretaceous formation show distinct gray to black color whereas Tertiary deposits have clays with color varying from pale yellow to brown to gray. All measured REEs exhibit lower concentrations than Upper Continental Crust (UCC) average values. Large variations in REEs contents were observed in different sedimentary formations (Tertiary and Cretaceous). Chondrite normalized ratio of La/Lu and Eu/Eu* indicate that the clays are derived from weathering of felsic rock and possibly under humid climate. All the samples showed positive Eu anomaly in North American Shale Composite (NASC) normalized plot which shows plagioclase feldspar as the major contributor to these clays. Positive Eu anomaly is also an indication of reduced condition of the formation. (author)

R and D programme on radioactive waste disposal into geological formations (study of a clay formation)

International Nuclear Information System (INIS)

Centre d'Etude de l'Energie Nucleaire, Mol

1987-01-01

This report deals with the R and D activities performed by the Belgian Nuclear Research Establishment (SCK/CEN) and its subcontractors concerning the disposal of high-level and long-life conditioned wastes in a deep clay formation, the Boom clay. The studies reported concern equally experimental as theoretical work spread over the following research issues: geochemical characterization of the Boom clay, modelling of radionuclide migration in the clay environment, irradiation effects and corrosion behaviour of candidate canister materials in the Boom clay, geomechanical, construction, backfilling and sealing studies related to underground facilities, regional hydrological investigations of the Mol site and safety and risk analysis. The geomechanical and construction-related studies are to a large extent focused on in situ research, performed along the construction of the underground Hades laboratory. The corrosion studies are also dealing with the preparation of in situ experiments in the same underground laboratory. These various research issues are meant to contribute to the assessment of the technical feasibility and safety of the geological disposal in an argillaceous host formation

Ball clay

Science.gov (United States)

Virta, R.L.

2001-01-01

Part of the 2000 annual review of the industrial minerals sector. A general overview of the ball clay industry is provided. In 2000, sales of ball clay reached record levels, with sanitary ware and tile applications accounting for the largest sales. Ball clay production, consumption, prices, foreign trade, and industry news are summarized. The outlook for the ball clay industry is also outlined.

Studies on Tagged Clay Migration Due to Water Movement

Energy Technology Data Exchange (ETDEWEB)

Scharpenseel, H. W. [Institut fuer Bodenkunde der Universitaet Bonn, Federal Republic of Germany (Germany); Kerpen, W. [Arbeitsgruppe, Institut fuer Landwirtschaft der KFA Juelich, Bonn, Federal Republic of Germany (Germany)

1967-11-15

{sup 55}Fe-tagged clay minerals, produced by hydrothermal synthesis, serve to clarify the question whether clay migration or clay formation in situ is the predominating mechanism in the B{sub t}-development of Parabraunerde (sol brun lessive, grey brown podsolic, hapludalf, dernopodsol). They further indicate the possibilities of clay transportation caused by water percolation. Suitable experimental approaches, such as thin-layer chromatography and autoradiography, translocation tests in columns filled with monotypical textural fractions or with undisturbed soil profiles, and synchronous hydrothermal treatment of {sup 55}Fe-con raining material from different horizons of Parabraunerde, to reveal the specific readiness of the different profile zones for {sup 55}Fe-clay production, are described. The possibilities of clay percolation are discussed. (author)

Comparison studies adsorption of thorium and uranium on pure clay minerals and local Malaysian soil sediments

International Nuclear Information System (INIS)

Syed, H.S.

1999-01-01

Adsorption studies of thorium and uranium radionuclides on 9 different pure clay minerals and 4 local Malaysian soil sediments were conducted. Solution containing dissolved thorium and uranium at pH 4.90 was prepared from concentrate sludges from a long term storage facility at a local mineral processing plant. The sludges are considered as low level radioactive wastes. The results indicated that the 9 clay minerals adsorbed more uranium than thorium at pH ranges from 3.74 to 5.74. Two local Malaysian soils were observed to adsorb relatively high concentration of both radionuclides at pH 3.79 to 3.91. The adsorption value 23.27 to 27.04 ppm for uranium and 33.1 to 50.18 ppm for thorium indicated that both soil sediments can be considered as potential enhanced barrier material for sites disposing conditioned wastes containing uranium and thorium. (author)

Proceedings of the NEA Clay Club Workshop on Clay characterisation from nanoscopic to microscopic resolution

International Nuclear Information System (INIS)

2013-01-01

A wide spectrum of argillaceous media are being considered in Nuclear Energy Agency (NEA) member countries as potential host rocks for the final, safe disposal of radioactive waste, and/or as major constituent of repository systems in which wastes will be emplaced. In this context, the NEA established the Working Group on the 'Characterisation, the Understanding and the Performance of Argillaceous Rocks as Repository Host Formations' in 1990, informally known as the 'Clay Club'. The Clay Club examines various argillaceous rocks that are being considered for the underground disposal of radioactive waste, ranging from soft clays to indurated shales. Very generally speaking, these clay rocks are composed of fine-grained minerals showing pore sizes from < 2 nm (micropores) up to > 50 nm (macro-pores). The water flow, solute transport and mechanical properties are largely determined by this microstructure, the spatial arrangement of the minerals and the chemical pore water composition. Examples include anion accessible ('geochemical') porosity and macroscopic membrane effects (chemical osmosis, hyper-filtration), geomechanical properties and the characteristics of two-phase flow properties (relevant for gas transport). At the current level of knowledge, there is a strong need to improve the nanoscale description of the phenomena observed at a more macroscopic scale. However, based on the scale of individual clay-minerals and pore sizes, for most of the imaging techniques this resolution is a clear challenge. The workshop, hosted by the Institute for Nuclear Waste Disposal (INE), Karlsruhe Institute of Technology (KIT) in the Akademiehotel Karlsruhe (Germany) from 6 to 8 September 2011, was intended to give, inter alia, a discussion platform on: - The current state-of-the-art of different spectro-microscopic methods - New developments addressing the above mentioned knowledge gaps in clays. - The perception of the interplay between geometry

Aqueous suspensions of natural swelling clay minerals. 2. Rheological characterization.

Science.gov (United States)

Paineau, Erwan; Michot, Laurent J; Bihannic, Isabelle; Baravian, Christophe

2011-06-21

We report in this article a comprehensive investigation of the viscoelastic behavior of different natural colloidal clay minerals in aqueous solution. Rheological experiments were carried out under both dynamic and steady-state conditions, allowing us to derive the elasticity and yield stress. Both parameters can be renormalized for all sizes, ionic strength, and type of clay using in a first approach only the volume of the particles. However, applying such a treatment to various clays of similar shapes and sizes yields differences that can be linked to the repulsion strength and charge location in the swelling clays. The stronger the repulsive interactions, the better the orientation of clay particles in flows. In addition, a master linear relationship between the elasticity and yield stress whose value corresponds to a critical deformation of 0.1 was evidenced. Such a relationship may be general for any colloidal suspension of anisometric particles as revealed by the analysis of various experimental data obtained on either disk-shaped or lath- and rod-shaped particles. The particle size dependence of the sol-gel transition was also investigated in detail. To understand why suspensions of larger particles gel at a higher volume fraction, we propose a very simplified view based on the statistical hydrodynamic trapping of a particle by an another one in its neighborhood upon translation and during a short period of time. We show that the key parameter describing this hydrodynamic trapping varies as the cube of the average diameter and captures most features of the sol-gel transition. Finally, we pointed out that in the high shear limit the suspension viscosity is still closely related to electrostatic interactions and follows the same trends as the viscoelastic properties. © 2011 American Chemical Society

Mineral carbonation of gaseous carbon dioxide using a clay-hosted cation exchange reaction.

Science.gov (United States)

Kang, Il-Mo; Roh, Ki-Min

2013-01-01

The mineral carbonation method is still a challenge in practical application owing to: (1) slow reaction kinetics, (2) high reaction temperature, and (3) continuous mineral consumption. These constraints stem from the mode of supplying alkaline earth metals through mineral acidification and dissolution. Here, we attempt to mineralize gaseous carbon dioxide into calcium carbonate, using a cation exchange reaction of vermiculite (a species of expandable clay minerals). The mineralization is operated by draining NaCI solution through vermiculite powders and continuously dropping into the pool of NaOH solution with CO2 gas injected. The mineralization temperature is regulated here at 293 and 333 K for 15 min. As a result of characterization, using an X-ray powder diffractometer and a scanning electron microscopy, two types of pure CaCO3 polymorphs (vaterite and calcite) are identified as main reaction products. Their abundance and morphology are heavily dependent on the mineralization temperature. Noticeably, spindle-shaped vaterite, which is quite different from a typical vaterite morphology (polycrystalline spherulite), forms predominantly at 333 K (approximately 98 wt%).

A new and improved methodology for qualitative and quantitative mineralogical analysis of Boom Clay

International Nuclear Information System (INIS)

Zeelmaekers, E.; Vandenberghe, N.; Honty, M.; De Craen, M.; Derkowski, A.; Van Geet, M.

2010-01-01

Document available in extended abstract form only. A good knowledge of the mineralogy of any host formation studied for geological disposal of high-level radioactive waste, is a prerequisite for understanding the geochemical environment which will determine the migration and retention behaviour of radionuclides. In this respect, the Boom Clay mineralogical composition has been extensively studied last decades as reference host formation (e.g. ARCHIMEDEARGILE project, OECD-NEA clay catalogue report) with the aim to provide reliable data for a safety assessment. However, a comparison of the available literature data clearly showed a serious discrepancy among studies, not only in the quantitative, but also in the qualitative mineralogical composition of the Boom Clay (SAFIR II). The reason for such a huge disagreement could be related, among others, to variable grain size distributions of the studied samples (sample heterogeneity) and differences in the methodological approaches. In particular, the unambiguous characterisation of clay minerals and the quantification of mixed-layer phases appeared as an everlasting problem. This study is aimed at achieving a consensus on the qualitative and quantitative mineralogical data of the Boom Clay using the most advanced techniques currently available in the clay science. A new sampling campaign was performed in such a way that samples are (20 in total) more or less regularly distributed over Boom Clay Formation, ensuring that variations in the grain size distributions due to silty clay-clayey silt layers alternations are accounted for. The novel concept based on an analysis at two levels was applied: (1) bulk rock and (2) clay fraction analysis. (1) A bulk rock analysis consists of conventional XRD analysis with the identification of the principal mineral phases. As a next step, the bulk rock was mixed with a ZnO internal standard and experimental diffraction patterns of randomly oriented powders were analyzed using &apos

Characterization of clay deposits from Egypt and assessment of their potential application for waste water treatment: How dissolved organic matter determines the interaction of heavy metals and clay minerals

NARCIS (Netherlands)

Refaey Mohammed, Y.B.

2016-01-01

The main aim of this study was to investigate the potential of using clay minerals abundant in local soils in Egypt as low cost materials to reduce Cu, Ni and Zn pollution of soil and groundwater originating from polluted wastewater; specifically focusing on the influence of the interaction of clay

Mineral formation on metallic copper in a `Future repository site environment`: Textural considerations based on natural analogs

Energy Technology Data Exchange (ETDEWEB)

Amcoff, Oe. [Uppsala Univ. (Sweden). Inst. of Earth Sciences

1998-01-01

Copper mineral formation in the Swedish `repository site environment` is discussed. Special attention is given to ore mineral textures (=the spatial relation among minerals), with examples given from nature. It is concluded: By analogy with observations from natural occurrences, an initial coating of Cu-oxide on the canister surface (because of entrapped air during construction) will probably not hinder a later sulphidation process. Early formation of Cu-sulphides on the canister surface may be accompanied by formation of CuFe-sulphides. The latter phase(s) may form through replacement of the Cu-sulphides or, alternatively, by means of reaction between dissolved copper and fine-grained iron sulphide (pyrite) in the surrounding bentonite. Should for some reason the bentonite barrier fail and the conditions become strongly oxidizing, we can expect crustifications and rhythmic growths of Cu(II)-phases, like malachite (Cu{sub 2}(OH){sub 2}CO{sub 3}). A presence of Fe{sup 2} in the clay minerals making up the bentonite might prove to have an adverse effect on the canister stability, since, in this case, the bentonite might be expected to act as a sink for dissolved copper. The mode of mineral growth along the copper - bentonite interface remains an open question.

Mineral formation on metallic copper in a 'Future repository site environment': Textural considerations based on natural analogs

International Nuclear Information System (INIS)

Amcoff, Oe.

1998-01-01

Copper mineral formation in the Swedish 'repository site environment' is discussed. Special attention is given to ore mineral textures (=the spatial relation among minerals), with examples given from nature. It is concluded: By analogy with observations from natural occurrences, an initial coating of Cu-oxide on the canister surface (because of entrapped air during construction) will probably not hinder a later sulphidation process. Early formation of Cu-sulphides on the canister surface may be accompanied by formation of CuFe-sulphides. The latter phase(s) may form through replacement of the Cu-sulphides or, alternatively, by means of reaction between dissolved copper and fine-grained iron sulphide (pyrite) in the surrounding bentonite. Should for some reason the bentonite barrier fail and the conditions become strongly oxidizing, we can expect crustifications and rhythmic growths of Cu(II)-phases, like malachite (Cu 2 (OH) 2 CO 3 ). A presence of Fe 2 in the clay minerals making up the bentonite might prove to have an adverse effect on the canister stability, since, in this case, the bentonite might be expected to act as a sink for dissolved copper. The mode of mineral growth along the copper - bentonite interface remains an open question

Modeling Coupled Processes in Clay Formations for Radioactive Waste Disposal

Energy Technology Data Exchange (ETDEWEB)

Liu, Hui-Hai; Rutqvist, Jonny; Zheng, Liange; Sonnenthal, Eric; Houseworth, Jim; Birkholzer, Jens

2010-08-31

As a result of the termination of the Yucca Mountain Project, the United States Department of Energy (DOE) has started to explore various alternative avenues for the disposition of used nuclear fuel and nuclear waste. The overall scope of the investigation includes temporary storage, transportation issues, permanent disposal, various nuclear fuel types, processing alternatives, and resulting waste streams. Although geologic disposal is not the only alternative, it is still the leading candidate for permanent disposal. The realm of geologic disposal also offers a range of geologic environments that may be considered, among those clay shale formations. Figure 1-1 presents the distribution of clay/shale formations within the USA. Clay rock/shale has been considered as potential host rock for geological disposal of high-level nuclear waste throughout the world, because of its low permeability, low diffusion coefficient, high retention capacity for radionuclides, and capability to self-seal fractures induced by tunnel excavation. For example, Callovo-Oxfordian argillites at the Bure site, France (Fouche et al., 2004), Toarcian argillites at the Tournemire site, France (Patriarche et al., 2004), Opalinus clay at the Mont Terri site, Switzerland (Meier et al., 2000), and Boom clay at Mol site, Belgium (Barnichon et al., 2005) have all been under intensive scientific investigations (at both field and laboratory scales) for understanding a variety of rock properties and their relations with flow and transport processes associated with geological disposal of nuclear waste. Clay/shale formations may be generally classified as indurated and plastic clays (Tsang et al., 2005). The latter (including Boom clay) is a softer material without high cohesion; its deformation is dominantly plastic. For both clay rocks, coupled thermal, hydrological, mechanical and chemical (THMC) processes are expected to have a significant impact on the long-term safety of a clay repository. For

Modeling Coupled Processes in Clay Formations for Radioactive Waste Disposal

International Nuclear Information System (INIS)

Liu, Hui-Hai; Rutqvist, Jonny; Zheng, Liange; Sonnenthal, Eric; Houseworth, Jim; Birkholzer, Jens

2010-01-01

As a result of the termination of the Yucca Mountain Project, the United States Department of Energy (DOE) has started to explore various alternative avenues for the disposition of used nuclear fuel and nuclear waste. The overall scope of the investigation includes temporary storage, transportation issues, permanent disposal, various nuclear fuel types, processing alternatives, and resulting waste streams. Although geologic disposal is not the only alternative, it is still the leading candidate for permanent disposal. The realm of geologic disposal also offers a range of geologic environments that may be considered, among those clay shale formations. Figure 1-1 presents the distribution of clay/shale formations within the USA. Clay rock/shale has been considered as potential host rock for geological disposal of high-level nuclear waste throughout the world, because of its low permeability, low diffusion coefficient, high retention capacity for radionuclides, and capability to self-seal fractures induced by tunnel excavation. For example, Callovo-Oxfordian argillites at the Bure site, France (Fouche et al., 2004), Toarcian argillites at the Tournemire site, France (Patriarche et al., 2004), Opalinus clay at the Mont Terri site, Switzerland (Meier et al., 2000), and Boom clay at Mol site, Belgium (Barnichon et al., 2005) have all been under intensive scientific investigations (at both field and laboratory scales) for understanding a variety of rock properties and their relations with flow and transport processes associated with geological disposal of nuclear waste. Clay/shale formations may be generally classified as indurated and plastic clays (Tsang et al., 2005). The latter (including Boom clay) is a softer material without high cohesion; its deformation is dominantly plastic. For both clay rocks, coupled thermal, hydrological, mechanical and chemical (THMC) processes are expected to have a significant impact on the long-term safety of a clay repository. For

Distribution of clay minerals in marine sediments off Chennai, Bay of Bengal, India: Indicators of sediment sources and transport processes .

Digital Repository Service at National Institute of Oceanography (India)

Veerasingam, S.; Venkatachalapathy, R.; Ramkumar, T.

Clay mineralogy, texture size and statistical analyses were carried out on surface sediments from the continental shelf of Chennai, Bay of Bengal, India. The purpose of this study is to characterize the clay mineral distribution and its relation...

The Imprint of Atmospheric Evolution in the D/H of Hesperian Clay Minerals on Mars

Science.gov (United States)

Mahaffy, P. R.; Webster, C. R.; Stern, J. C.; Brunner, A. E.; Atreya, S. K.; Conrad, P. G.; Domagal-Goldman, S.; Eigenbrode, J. L.; Flesch, G. J.; Christensen, L. E.;

Reconstruction of late Quaternary monsoon oscillations based on clay mineral proxies using sediment cores from the western margin of India

Digital Repository Service at National Institute of Oceanography (India)

Thamban, M.; Rao, V.P.; Schneider, R.R.

sites were from the hinterland rocks and soils. Careful evaluations of several factors that could complicate the clay distribution in marine environment indicate that the clay mineral parameters can be used as proxies for the intensity of summer monsoon...

Methylene blue adsorption in clay mineral dealt with organic cation; Sorcao de azul de metileno em argila esmectitica tratada com cation organico

Energy Technology Data Exchange (ETDEWEB)

Silva, T.L. [Universidade Federal do Para (UFPA), Maraba, PA (Brazil). Faculdade de Engenharia de Materiais; Lemos, V.P., E-mail: tls1981@hotmail.com [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Centro de Geociencias

2011-07-01

The interaction among organic cations, as the methylene blue (AM) and benzyltrimethylammonium (BTMA), and clay minerals of the group of the smectite they result in the formation of applied materials in the adsorption of organic pollutant presents in waters, soils and you cultivate. In this work they were prepared the adsorbents (organic-clays) smectite - AM and smectite-BTMA. The precursory sample of smectite was collected in Rio Branco-Acre. We were also used an smectite sample collected in Sena Madureira (SM)-Acre already characterized in previous work and a sample of standard smectite Swy-2-Na-Montmorillonite (SWy-2) of Wymong - USA. The organic agents selected for this study they were: Blue of Methylene, denominated AM and Benzyltrimethylammonium, denominated BTMA. They were appraised the capacities adsorptive of the treated samples with BTMA being used AM as adsorbate. The results of these evaluations detected that ran total adsorption of AM (concentrations varying from 1 to 10 ppm) for the treated samples with BTMA. The organic cation, BTMA, interacting with the surfaces of the natural clay was more efficient in the adsorption of AM than the clay without the previous treatment with this salt. (author)

Hydrothermal Synthesis of Analcime from Kutingkeng Formation Mudstone

Science.gov (United States)

Hsiao, Yin-Hsiu; Chen, Kuan-Ting; Ray, Dah-Tong

2015-04-01

In southwest of Taiwan, the foothill located in Tainan-Kaohsiung city is the exposed area of Pliocene strata to early Pleistocene strata. The strata are about a depth of five thousand, named as Kutigkeng Formation. The outcrop of Kutigkeng Formation is typical badlands, specifically called 'Moon World.' It is commonly known as no important economic applications of agricultural land. The mineral compositions of Kutingkeng Formation are quartz, clay minerals and feldspar. The clay minerals consist of illite, clinochlore and swelling clays. To study how the phase and morphology of analcime formed by hydrothermal synthesis were affected, analcime was synthesized from the mudstone of Kutinkeng Formation with microwave hydrothermal reaction was investigated. The parameters of the experiment were the reaction temperature, the concentration of mineralizer, solids/liquid ratio and time. The sodium silicate (Na2SiO3) were used as mineralizer. The results showed that the analcime could be synthesized by hydrothermal reaction above 180° from Kutinkeng Formation mudstone samples. At the highest temperature (240°) of this study, the high purity analcime could be produced. When the concentration of Na2SiO3=3~6M, analcime could be synthesized at 240°. The best solids/liquid ratio was approximate 1 to 5. The hydrothermal reaction almost was completed after 4 hours.

Transmission X-ray Microscopy—A New Tool in Clay Mineral Floccules Characterization

Directory of Open Access Journals (Sweden)

Ray L. Frost

2012-10-01

Full Text Available Effective flocculation and dewatering of mineral processing streams containing clays are microstructure dependent in clay-water systems. Initial clay flocculation is crucial in the design and for the development of a new methodology of gas exploitation. Microstructural engineering of clay aggregates using covalent cations and Keggin macromolecules have been monitored using the new state of the art Transmission X-ray Microscope (TXM with 60 nm tomography resolution installed in a Taiwanese synchrotron. The 3-D reconstructions from TXM images show complex aggregation structures in montmorillonite aqueous suspensions after treatment with Na+, Ca2+ and Al13 Keggin macromolecules. Na-montmorillonite displays elongated, parallel, well-orientated and closed-void cellular networks, 0.5–3 µm in diameter. After treatment by covalent cations, the coagulated structure displays much smaller, randomly orientated and openly connected cells, 300–600 nm in diameter. The average distances measured between montmorillonite sheets was around 450 nm, which is less than half of the cell dimension measured in Na-montmorillonite. The most dramatic structural changes were observed after treatment by Al13 Keggin; aggregates then became arranged in compacted domains of a 300 nm average diameter composed of thick face-to-face oriented sheets, which forms porous aggregates with larger intra-aggregate open and connected voids.

Mineral formation and organo-mineral controls on the bioavailability of carbon at the terrestrial-aquatic interface

Science.gov (United States)

Rod, K. A.; Smith, A. P.; Renslow, R.

2016-12-01

Recent evidence highlights the importance of organo-mineral interactions in regulating the source or sink capacity of soil. High surface area soils, such as allophane-rich or clay-rich soils, retain organic matter (OM) via sorption to mineral surfaces which can also contribute physical isolation in interlayer spaces. Despite the direct correlation between mineral surfaces and OM accumulation, the pedogenic processes controlling the abundance of reactive surface areas and their distribution in the mineral matrix remains unclear. As global soil temperatures rise, the dissolution of primary minerals and formation of new secondary minerals may be thermodynamically favored as part of soil weathering process. Newly formed minerals can supply surfaces for organo-metallic bonding and may, therefore, stabilize OM by surface bonding and physical exclusion. This is especially relevant in environments that intersect terrestrial and aquatic systems, such as the capillary fringe zone in riparian ecosystems. To test the mechanisms of mineral surface area protection of OM, we facilitated secondary precipitation of alumino-silicates in the presence of OM held at two different temperatures in natural Nisqually River sediments (Mt Rainier, WA). This was a three month reaction intended to simulate early pedogenesis. To tease out the influence of mineral surface area increase during pedogenesis, we incubated the sediments at two different soil moisture contents to induce biodegradation. We measured OM desorption, biodegradation, and the molecular composition of mineral-associated OM both prior to and following the temperature manipulation. To simulate the saturation of capillary fringe sediment and associated transport and reaction of OM, column experiments were conducted using the reacted sediments. More co-precipitation was observed in the 20°C solution compared to the 4°C reacted solution suggesting that warming trends alter mineral development and may remove more OM from solution

Clay mineral distribution in the continental shelf and slope off Saurashtra, West coast of India

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P.

Clay mineral distribution in the sediments of the west coast of India indicates that the illite and chlorite-rich sediments, derived from the Indus, occupy the continental shelf of the northern part of the Gulf of Kutch. Montmorillonite derived from...

Iodide uptake by negatively charged clay interlayers?

Science.gov (United States)

Miller, Andrew; Kruichak, Jessica; Mills, Melissa; Wang, Yifeng

2015-09-01

Understanding iodide interactions with clay minerals is critical to quantifying risk associated with nuclear waste disposal. Current thought assumes that iodide does not interact directly with clay minerals due to electrical repulsion between the iodide and the negatively charged clay layers. However, a growing body of work indicates a weak interaction between iodide and clays. The goal of this contribution is to report a conceptual model for iodide interaction with clays by considering clay mineral structures and emergent behaviors of chemical species in confined spaces. To approach the problem, a suite of clay minerals was used with varying degrees of isomorphic substitution, chemical composition, and mineral structure. Iodide uptake experiments were completed with each of these minerals in a range of swamping electrolyte identities (NaCl, NaBr, KCl) and concentrations. Iodide uptake behaviors form distinct trends with cation exchange capacity and mineral structure. These trends change substantially with electrolyte composition and concentration, but do not appear to be affected by solution pH. The experimental results suggest that iodide may directly interact with clays by forming ion-pairs (e.g., NaI(aq)) which may concentrate within the interlayer space as well as the thin areas surrounding the clay particle where water behavior is more structured relative to bulk water. Ion pairing and iodide concentration in these zones is probably driven by the reduced dielectric constant of water in confined space and by the relatively high polarizability of the iodide species. Copyright © 2015 Elsevier Ltd. All rights reserved.

Effect of clay minerals on the stabilization of black cotton and lateritic soils

International Nuclear Information System (INIS)

Nyambok, I.O.

1986-01-01

The problem associated with black cotton and lateritic soils because of the swelling-shrinkage property of their constituent clay minerals were investigated. Samples of black cotton lateritic soils were collected from different parts of Kenya. The samples were analysed for their mineral compositions and later treated with hydrated lime in order to eliminate the swelling shrinkage behaviour. The samples were subsequently tested for their engineering properties in a soil mechanics laboratory using shear box and Casagrande apparatus. It was found that the chemical treatment of the soils with hydrated lime removes their plastic property and improves their shear strength. (author)

Modeling selenate adsorption behavior on oxides, clay minerals, and soils using the triple layer model

Science.gov (United States)

Selenate adsorption behavior was investigated on amorphous aluminum oxide, amorphous iron oxide, goethite, clay minerals: kaolinites, montmorillonites, illite, and 18 soil samples from Hawaii, and the Southwestern and the Midwestern regions of the US as a function of solution pH. Selenate adsorpti...

Correlation between thermal behavior of clays and their chemical and mineralogical composition: a review

Science.gov (United States)

Dwi Yanti, Evi; Pratiwi, I.

2018-02-01

Clay's abundance has been widely used as industrial raw materials, especially ceramic and tile industries. Utilization of these minerals needs a thermal process for producing ceramic products. Two studies conducted by Septawander et al. and Chin C et al., showed the relationship between thermal behavior of clays and their chemical and mineralogical composition. Clays are characterized by XRD analysis and thermal analysis, ranging from 1100°C to 1200°C room temperature. Specimen of raw materials of clay which is used for the thermal treatment is taken from different geological conditions and formation. In raw material, Quartz is almost present in all samples. Halloysite, montmorillonite, and feldspar are present in Tanjung Morawa raw clay. KC and MC similar kaolinite and illite are present in the samples. The research illustrates the interrelationships of clay minerals and chemical composition with their heat behavior. As the temperature of combustion increases, the sample reduces a significant weight. The minerals which have undergone a transformation phase became mullite, cristobalite or illite and quartz. Under SEM analysis, the microstructures of the samples showed irregularity in shape; changes occurred due the increase of heat.

Luminescent Oxygen Gas Sensors Based on Nanometer-Thick Hybrid Films of Iridium Complexes and Clay Minerals

Directory of Open Access Journals (Sweden)

Hisako Sato

2014-01-01

Full Text Available The use of Ir(III complexes in photo-responsive molecular devices for oxygen gas sensing is reviewed. Attention is focused on the immobilization of Ir(III complexes in organic or inorganic host materials such as polymers, silica and clays in order to enhance robustness and reliability. Our recent works on constructing nanometer-thick films comprised of cyclometalated cationic Ir(III complexes and clay minerals are described. The achievement of multi-emitting properties in response to oxygen pressure is demonstrated.

Study on rich alumina alkali-activated slag clay minerals cementitious materials for immobilization of radioactive waste

International Nuclear Information System (INIS)

Li Yuxiang; Qian Guangren; Yi Facheng; Shi Rongming; Fu Yibei; Li Lihua; Zhang Jun

1999-01-01

The composition and some properties of its pastes of rich alumina alkali-activated slag clay minerals (RAAASCM) cementitious materials for immobilization of radioactive waste are studied. Experimental results show that heat activated kaolinite, Xingjiang zeolite, modified attapulgite clay are better constituents of RAAASCM. RAAASCM cementitious materials pastes exhibit high strength, low porosity, fewer harmful pore, and high resistance to sulphate corrosion as well as gamma irradiation. The Sr 2+ , Cs + leaching portion of the simulated radioactive waste forms based on RAAASCM, is low

Polymer-clay nanocomposites obtained by solution polymerization ...

Indian Academy of Sciences (India)

Clay minerals can be found all over the world.1 Clay minerals have ... salts or covalent bonding with silanes at the OH edges of the clay. ..... Marras S I, Tsimpliaraki A, Zuburtikudis I and ... Mansoori Y, Roojaei K, Zamanloo M R and Imanzadeh.

Visible-near-infrared spectroscopy can predict the clay/organic carbon and mineral fines/organic carbon ratios

DEFF Research Database (Denmark)

Hermansen, Cecilie; Knadel, Maria; Møldrup, Per

2016-01-01

The ratios of mineral fines (carbon (OC), consisting of the n-ratio (i.e., the clay/OC ratio) and m-ratio (i.e., the fines/OC ratio) have recently been used to analyze and predict soil functional properties such as tilth conditions, clay dispersibility, degree...... from seven Danish and one Greenlandic fields, with a large textural range (clay: 0.027–0.355 kg kg−1; OC: 0.011–0.084 kg kg−1; n-ratio: 0.49–16.80; m-ratio: 1.46–32.14), were analyzed for texture and OC and subsequently scanned with a vis-NIR spectrometer from 400 to 2500 nm. The spectral data were...

Evidence of cyclic climatic changes recorded in clay mineral assemblages from a continental Paleocene-Eocene sequence, northwestern Argentina

Science.gov (United States)

Do Campo, Margarita; Bauluz, Blanca; del Papa, Cecilia; White, Timothy; Yuste, Alfonso; Mayayo, Maria Jose

2018-06-01

The continental Paleocene-Eocene sequence investigated in this study belongs to the Salta Group, deposited in an intracontinental rift, the Salta Basin (NW Argentina), that evolved from the lower Cretaceous to the middle Paleogene, and is subdivided into the Pirgua, the Balbuena and the Santa Barbara Subgroups. The Maíz Gordo Formation (200 m thick) is the middle unit of the Santa Bárbara Subgroup, deposited during late post-rift sedimentation. We studied the mineralogy of fine-grained horizons of this formation by X-ray diffraction and Scanning Electron Microscopy (SEM) in order to examine the connection between vertical changes in clay mineralogy in alluvial sediments and paleosols, and global paleoclimatic changes registered during the Paleogene. Paleosols vary from calcic vertisols in the lowermost levels, to inseptisols and gleysols in intermediate positions, to gleyed oxisols in the upper section, indicating increased chemical weathering through time. Clay mineral relative abundances vary with a general increase in kaolinite content from bottom to top. However, at one site there are significant variations in kaolinite/muscovite (Kln/Ms) that define five cycles of kaolinite abundance and Kln/Ms. that indicate cyclic patterns of paleoprecipitation and paleotemperature. These are interpreted as several short-lived hyperthermals during the Paleocene-early Eocene in the Southern Hemisphere, which correlate with well-established episodes of warmth documented from the Northern Hemisphere.

X-ray-phase and IR-spectral study of clay rocks mineral content of the Caspian Sea Gulf depression

International Nuclear Information System (INIS)

Zakonov, A.N.; Mukhanova, M.U.

2000-01-01

Samples of clays selected from different oil fields (Sazankurak, Kemerkol, Kozha and others) and deposition depths are examined on both the X-ray diffractometers (Dron-2 and Dron-4) and the infrared-spectrometers (IR-20). In this diagnostic the American file with different minerals X-ray systematized data is used. The X-ray reflections, which are in compliance with suitable inter-plane distances and clay impurities reflex intensities are determined. With confirmation purpose for mineral content correctness obtained according X-ray-phase analysis the infrared-spectrometric method is used, in which principal attention was paid to absorption field (3,400-3,700 cm -1 ) of H 2 O and OH valency frequency vibrations

Selection of a site adapted to the realization of an underground laboratory in clay formations

International Nuclear Information System (INIS)

Benvegnu, F.

1984-01-01

Research carried out in Italy by ENEA for site selection of an underground laboratory in a clay formation are presented. Mine roadways, abandoned tunnels, natural or artificial escarpments are prospected. The Pasquasia potash mine in Sicily was selected. The decline reach the lower pliocen starta from -110m to -200m below surface through a clay formation. The site selected for the laboratory is 160 m deep. A 50 meter-long horizontal tunnel will be dug. Experiments planned include thermal, hydrological, mechanical and thermomechanical behavior of clays. Data on temperature variations, interstitial fluid pressure, total pressure, deformations produced by a heater placed in clay will be obtained. Data related to mechanical behavior of formation will be recorded before, during and after the construction of the gallerie. Convergence of borehole will be also studied

Mars, clays and the origins of life

Science.gov (United States)

Hartman, Hyman

1989-01-01

To detect life in the Martian soil, tests were designed to look for respiration and photosynthesis. Both tests (labeled release, LR, and pyrolytic release, PR) for life in the Martian soils were positive. However, when the measurement for organic molecules in the soil of Mars was made, none were found. The interpretation given is that the inorganic constituents of the soil of Mars were responsible for these observations. The inorganic analysis of the soil was best fitted by a mixture of minerals: 60 to 80 percent clay, iron oxide, quartz, and soluble salts such as halite (NaCl). The minerals most successful in simulating the PR and LR experiments are iron-rich clays. There is a theory that considers clays as the first organisms capable of replication, mutation, and catalysis, and hence of evolving. Clays are formed when liquid water causes the weathering of rocks. The distribution of ions such as aluminum, magnesium, and iron play the role of bases in the DNA. The information was stored in the distribution of ions in the octahedral and tetrahedral molecules, but that they could, like RNA and DNA, replicate. When the clays replicated, each sheet of clay would be a template for a new sheet. The ion substitutions in one clay sheet would give rise to a complementary or similar pattern on the clay synthesized on its surface. It was theorized that it was on the surface of replicating iron-rich clays that carbon dioxide would be fixed in the light into organic acids such as formic or oxalic acid. If Mars had liquid water during a warm period in its past, clay formation would have been abundant. These clays would have replicated and evolved until the liquid water was removed due to cooling of Mars. It is entirely possible that the Viking mission detected life on Mars, but it was clay life that awaits the return of water to continue its evolution into life based on organic molecules.

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

Primordial clays on Mars formed beneath a steam or supercritical atmosphere.

Science.gov (United States)

Cannon, Kevin M; Parman, Stephen W; Mustard, John F

2017-12-06

On Mars, clay minerals are widespread in terrains that date back to the Noachian period (4.1 billion to 3.7 billion years ago). It is thought that the Martian basaltic crust reacted with liquid water during this time to form hydrated clay minerals. Here we propose, however, that a substantial proportion of these clays was formed when Mars' primary crust reacted with a dense steam or supercritical atmosphere of water and carbon dioxide that was outgassed during magma ocean cooling. We present experimental evidence that shows rapid clay formation under conditions that would have been present at the base of such an atmosphere and also deeper in the porous crust. Furthermore, we explore the fate of a primordial clay-rich layer with the help of a parameterized crustal evolution model; we find that the primordial clay is locally disrupted by impacts and buried by impact-ejected material and by erupted volcanic material, but that it survives as a mostly coherent layer at depth, with limited surface exposures. These exposures are similar to those observed in remotely sensed orbital data from Mars. Our results can explain the present distribution of many clays on Mars, and the anomalously low density of the Martian crust in comparison with expectations.

Sorption of radionuclides by tertiary clays

International Nuclear Information System (INIS)

Wagner, J.F.; Czurda, K.A.

1990-01-01

The sorption capacity of different clay types for some metals (Co, Cs, Sr and Zn), occurring as common radionuclides in radioactive waste deposits, had been analysed by a static (batch technique) and a dynamic method (percolation tests, in which the driving force is a hydraulic gradient). Sorption capacity generally increased with an increasing pH of solution. A decrease of sorption capacity had been observed in the order Zn > Cs ≥ Co > Sr for the batch and Cs > Zn > Sr > Co for the percolation tests. Clay marls showed a distinctly higher sorption respectively retention capacity as pure clays. Sorption capacity depends on solution parameters like type and concentration of radionuclide, pH, salt concentration, etc., and on rock parameters like mineral content (e.g. swelling clay minerals and carbonates), organic material, rock pH, micro fabric, etc. A third parameter of great influence is the contact time between clay and solution. The adsorption isotherms reflect two different adsorption mechanisms: a very rapid adsorption (a few minutes) on the external surfaces of clay minerals and a slow adsorption process (weeks and longer), due to the diffusion of metal ions into the interlayer space of clay minerals. 12 refs., 9 figs., 1 tab

Iron-clay interactions under a thermal gradient

International Nuclear Information System (INIS)

Jodin-Caumon, Marie-Camille; Mosser-Ruck, Regine; Randi, Aurelien; Cathelineau, Michel; Michau, Nicolas

2010-01-01

Document available in extended abstract form only. Repository in deep geological formations is considered as a possible solution for long-term high-level nuclear waste (HLW) management. The concept generally consists in a multiple barriers system including steel canister in a clay host rock. Heat and radiation emissions by HLW, corrosion of the canister and desaturation/re-saturation of the clay may affect the properties of the geological formation. In this context, the possible mineralogical evolutions of clays in contact with metal iron were studied in various conditions simulating those of HLW repository. Most of these studies were carried out at a constant temperature whereas the system will undergo a thermal gradient in time (progressive decrease of the temperature of the HLW with the decrease of its activity) and space (from the waste to the host rock). A thermal gradient may imply mass transport phenomena by convection and diffusion processes as a function of temperature, gradient intensity and the nature of the chemical elements. Here we show the effect of a thermal gradient in space on the interaction between the argillite from the ANDRA underground laboratory at Bure (Meuse/Haute-Marne) and metal iron. Tube-in-tube experiments were carried out. Argillite was put in two previously drilled platinum capsules (Diam. holes: 200 μm). Metal iron (powder and plate) was added in one of the Pt capsule. The Pt capsules were then loaded at the two ends of a gold tube. A fluid (H 2 O or a saline solution) was added and the gold tube was sealed and regularly pinched to form 5 precipitation niches. The iron/argillite mass ratio ranged between 0.3 and 0.5 and the fluid/argillite mass ratio was around 10. A thermal gradient 80 deg. C-150 deg. C or 150 deg. C-300 deg. C was applied to the tube during 3 and 6 months. The end of the gold tube with the Pt capsule containing iron was placed at the hot point (max. temperature 150 deg. C or 300 deg. C) or at the cold point (min

Petrography, Geochemistry and Proposed Genesis of Ordovician Oolitic Iron Formation Members of the Lashkarak Formation, Eastern Alborz

International Nuclear Information System (INIS)

Maghsoudloo Mahalli, M.; Shafiei Bafti, B.

2016-01-01

Mineralogical characteristics combined with geochemical data show that anomalous values of Fe in studied carbonate argillite formations with respect to common sedimentary rocks are related to the abundance of iron-bearing oolites as oxides such as hematite and goethite, and the clay mineral chamosite. Based on Fe, Mg and Ca concentrations, oolitic iron formations can be divided into low-grade and high-grade iron formations. The former is characterized by chamosite and calcite, whereas the latter consists ofhematite and calcite. This research, along with available paleo-geographic and sedimentological information suggests that the iron for the formation of iron oolites was available from normal sea water and Fe could be carried as clastic particles along with clays or coating of clay particles derived from weathering and erosion of shales from adjacent land. High contents of K and Si in oolitic iron horizons, the presence of detrital zircon, quartz and clay minerals within oolites and also in the matrix of these rocks confirm the proposed model and show the important role of Fe-bearing clay minerals in the genesis of the primary chamositic oolites in an environment with p H=5-9 and medium-weak redox conditions (Maynard, 1983; Maynard, 1986). The abundance of hematite relative to goethite in the Fe-oolites, dense and elliptical oolites as well as the frequent occurrence of calcite veinlets cutting oolite beds has been attributed to diagenetic processes and the modification of chamosite and goethite to hematite. Our findings indicate that the studied members can be classified as low-grade oolitic iron formation (average 21 wt.% Fe) which do not have economic importance at present.

Use of clay-mineral alteration patterns to define syntectonic permeability of joints (cleat) in Pennsylvania anthracite coal

Energy Technology Data Exchange (ETDEWEB)

Daniels, E.J.; Marshak, S.; Altaner, S.P. [Chevron Oil Field Research Company, La Habra, CA (United States)

1996-10-15

Joints (cleat) in Pennsylvania anthracite contain two distinct clay-mineral assemblages, both of which formed by alteration of preexisting kaolinite at peak metamorphic conditions during the Alleghanian orogeny. The first assemblage, NH{sub 4} - illite or pyrophyllite {+-} quartz, formed by reaction of kaolinite with methane-rich fluids derived from within the coal. The second assemblage, sudoite {+-} tosudite {+-} rectorite {+-} berthierine, formed by the reaction of kaolinite with ferromagnesian-bearing hydrothermal fluids which must have come from outside the coal. In an earlier paper, the authors suggested that the first assemblage indicated clay diagenesis in low-permeability environments, and that the second assemblage indicated clay diagenesis in high-permeability environments. If this premise is correct, then the distribution of clay-mineral alteration assemblages serves to define syntectonic permeability variations in coal cleat. The first assemblage dominates in the coal matrix itself, in isolated cleat, in cleat that parallel the regional trend of Alleghanian folds, and in the mirror portions of cleat oriented perpendicular to the fold trends, suggesting that these regions are low-permeability environments. The second assemblage dominates in the hackle fringe of interconnected cleat that trend perpendicular to the strike of the Appalachian orogen, suggesting that these regions are high-permeability environments. These results emphasize that syntectonic cleat permeability is a function of cleat orientation, macroscopic cleat interconnetivity and orientation, as well as microscopic cleat-surface morphology.

Technetium migration in Boom Clay - Assessing the role of colloid-facilitated transport in a deep clay formation

International Nuclear Information System (INIS)

Bruggeman, C.; Martens, E.; Maes, N.; Jacops, E.; Van Gompel, M.; Van Ravestyn, L.

2010-01-01

Document available in extended abstract form only. The role of colloids - mainly dissolved natural organic matter (NOM, 50-150 mg/l) - in the transport of radionuclides in the Boom Clay formation (Mol, Belgium), has long since been a matter of (heavy) debate. For more than 20 years, batch experiments with Boom Clay suspensions showed a pronounced influence of the dissolved organic carbon concentration on the aqueous concentrations of different radionuclides like Tc, Np, Am and U. Moreover, small fractions of these radionuclides were also observed to elute almost un-retarded out of confined clay cores in percolation experiments. In the past years, a new conceptual model for the speciation of the long-lived fission product Technetium- 99 ( 99 Tc) under Boom Clay conditions has been drafted. In brief, the stable oxidation state of 99 Tc in these conditions is +IV, and, therefore, Tc solution concentrations are limited by the solubility of TcO 2 .nH 2 O(s). However, during reduction of TcVII (in the TcO 4 - form) to TcIV, precursor TcO 2 .nH 2 O colloids are formed, which are stabilised by the dissolved organic matter present in Boom Clay interstitial pore water, and in supernatants of Boom Clay batch suspensions. Moreover, this stabilisation process occurs in such a systematic way, that (conditional) interaction constants could be established, and the behaviour was described as a 'hydrophobic sorption', or, more accurately, a 'colloid-colloid' interaction. This conceptual model was implemented into PHREEQC geochemical and Hydrus transport code to come to a reactive transport model that was used to simulate both the outflow and the tracer profile in several long-term running percolation experiments (both in lab and under in situ conditions). To account for slow dissociation kinetics of Tc from the NOM colloid, a first-order kinetic rate equation was also added to the model. In order to describe the migration of colloidal particles (NOM), an

Clay mineral distribution in the shelf sediments off the northern part of the east coast of india

Digital Repository Service at National Institute of Oceanography (India)

Rao, V.P.; Reddy, N.P.C.; Rao, Ch.M.

Forty-eight sediment samples from the continental shelf between Visakhapatnam and the Ganges were analysed by X-ray diffraction for the composition and distribution of clay minerals. Estuarine samples of the Hooghly are dominated by illite...

Redox properties of structural Fe in clay minerals: 3. Relationships between smectite redox and structural properties.

Science.gov (United States)

Gorski, Christopher A; Klüpfel, Laura E; Voegelin, Andreas; Sander, Michael; Hofstetter, Thomas B

2013-01-01

Structural Fe in clay minerals is an important redox-active species in many pristine and contaminated environments as well as in engineered systems. Understanding the extent and kinetics of redox reactions involving Fe-bearing clay minerals has been challenging due to the inability to relate structural Fe(2+)/Fe(total) fractions to fundamental redox properties, such as reduction potentials (EH). Here, we overcame this challenge by using mediated electrochemical reduction (MER) and oxidation (MEO) to characterize the fraction of redox-active structural Fe (Fe(2+)/Fe(total)) in smectites over a wide range of applied EH-values (-0.6 V to +0.6 V). We examined Fe(2+)/Fe(total )- EH relationships of four natural Fe-bearing smectites (SWy-2, SWa-1, NAu-1, NAu-2) in their native, reduced, and reoxidized states and compared our measurements with spectroscopic observations and a suite of mineralogical properties. All smectites exhibited unique Fe(2+)/Fe(total) - EH relationships, were redox active over wide EH ranges, and underwent irreversible electron transfer induced structural changes that were observable with X-ray absorption spectroscopy. Variations among the smectite Fe(2+)/Fe(total) - EH relationships correlated well with both bulk and molecular-scale properties, including Fe(total) content, layer charge, and quadrupole splitting values, suggesting that multiple structural parameters determined the redox properties of smectites. The Fe(2+)/Fe(total) - EH relationships developed for these four commonly studied clay minerals may be applied to future studies interested in relating the extent of structural Fe reduction or oxidation to EH-values.

Radiation-induced defects in clay minerals, markers of the mobility of the uranium in solution in the unconformity-type uranium deposits

International Nuclear Information System (INIS)

Morichon, E.

2008-10-01

This study presents the works driven on three groups of clay minerals (kaolins, illite, sudoite (di-tri-octahedral chlorites)) characteristics of the alteration halos surrounding unconformity-type uranium deposits, in order to reveal uranium paleo-circulations in the intra-cratonic meso-Proterozoic basins (1,2 - 1,6 Ga). Thanks to Electron Paramagnetic Resonance Spectroscopy (EPR), we were able to highlight the persistence of structural defects in kaolin-group minerals contemporaneous of the basin diagenesis, and demonstrate the existence of relatively stable defects in illites and sudoites contemporaneous of the uranium deposits setting. Thus, the main defect in illite (Ai centre) and the main defect in sudoite (As centre) are characterized by their g components such as, respectively, gt = 2,003 et g// = 2,051 for illite and gt = 2,008 et g// = 2,051 for sudoite. As the main defect in kaolins (kaolinite/dickite), the main defects in illite and sudoite are perpendicularly oriented according to the (ab) plane, on the tetrahedral Si-O bound. However, their thermal stabilities seem different. The observation of samples from different zones (background, anomal or mineralized) of the Athabasca basin (Canada) allowed to identify a parallel evolution between actual defects concentration measured in the different clay minerals and the proximity of the mineralisation zones. Consequently, clays minerals can be considered as potential plotters of zones where uranium-rich solutions have circulated. (author)

Mineralogical characterization of Greda clays and monitoring of their phase transformations on thermal treatment

International Nuclear Information System (INIS)

Chavez Panduro, E.; Bravo Cabrejos, J.

2010-01-01

The mineralogical characterization of two clay samples from the Central Andean Region of Peru, denominated White Greda and Red Greda, is reported. These clays contain the clay minerals mica and illite respectively. Both clays were treated thermally in an oxidising atmosphere under controlled conditions up to 1,100 deg. C with the purpose of obtaining information about structural changes that may be useful for pottery manufacture. X-ray fluorescence was used for the elemental characterization of the samples and X-ray diffractometry was used to determine the collapse and formation of the mineral phases present in the samples caused by thermal treatment. At temperatures above 1,000 deg. C it is observed the formation of spinel in the case of White Greda and of hematite, corundum and cristobalite in the case of Red Greda. Room temperature transmission Moessbauer spectroscopy allowed the monitoring of the variation of the hyperfine parameters with the thermal treatment temperature; In the case of the evolution of the quadruple splitting of the paramagnetic Fe 3+ sites with temperature, in both clays, the analyses reproduced results such as the 'camel back' curve shape, found by other workers (Wagner and Wagner, Hyperfine Interact 154:35-82, 2004; Wagner and Kyek, Hyperfine Interact 154:5-33, 2004).

Mineralogical characterization of Greda clays and monitoring of their phase transformations on thermal treatment

Science.gov (United States)

Panduro, E. Chavez; Cabrejos, J. Bravo

2010-01-01

The mineralogical characterization of two clay samples from the Central Andean Region of Peru, denominated White Greda and Red Greda, is reported. These clays contain the clay minerals mica and illite respectively. Both clays were treated thermally in an oxidising atmosphere under controlled conditions up to 1,100°C with the purpose of obtaining information about structural changes that may be useful for pottery manufacture. X-ray fluorescence was used for the elemental characterization of the samples and X-ray diffractometry was used to determine the collapse and formation of the mineral phases present in the samples caused by thermal treatment. At temperatures above 1,000°C it is observed the formation of spinel in the case of White Greda and of hematite, corundum and cristobalite in the case of Red Greda. Room temperature transmission Mössbauer spectroscopy allowed the monitoring of the variation of the hyperfine parameters with the thermal treatment temperature; In the case of the evolution of the quadruple splitting of the paramagnetic Fe3 + sites with temperature, in both clays, the analyses reproduced results such as the “camel back” curve shape, found by other workers (Wagner and Wagner, Hyperfine Interact 154:35-82, 2004; Wagner and Kyek, Hyperfine Interact 154:5-33, 2004).

Mineralogical characterization of Greda clays and monitoring of their phase transformations on thermal treatment

Energy Technology Data Exchange (ETDEWEB)

Chavez Panduro, E., E-mail: 04130127@unmsm.edu.pe; Bravo Cabrejos, J., E-mail: jbravoc@unmsm.edu.pe [Universidad Nacional Mayor de San Marcos, Facultad de Ciencias Fisicas (Peru)

2010-01-15

The mineralogical characterization of two clay samples from the Central Andean Region of Peru, denominated White Greda and Red Greda, is reported. These clays contain the clay minerals mica and illite respectively. Both clays were treated thermally in an oxidising atmosphere under controlled conditions up to 1,100 deg. C with the purpose of obtaining information about structural changes that may be useful for pottery manufacture. X-ray fluorescence was used for the elemental characterization of the samples and X-ray diffractometry was used to determine the collapse and formation of the mineral phases present in the samples caused by thermal treatment. At temperatures above 1,000 deg. C it is observed the formation of spinel in the case of White Greda and of hematite, corundum and cristobalite in the case of Red Greda. Room temperature transmission Moessbauer spectroscopy allowed the monitoring of the variation of the hyperfine parameters with the thermal treatment temperature; In the case of the evolution of the quadruple splitting of the paramagnetic Fe{sup 3+} sites with temperature, in both clays, the analyses reproduced results such as the 'camel back' curve shape, found by other workers (Wagner and Wagner, Hyperfine Interact 154:35-82, 2004; Wagner and Kyek, Hyperfine Interact 154:5-33, 2004).

Processes of cation migration in clay-rocks: Final Scientific Report of the CatClay European Project

International Nuclear Information System (INIS)

Altmann, S.; Aertsens, M.; Appelo, T.; Bruggeman, C.; Gaboreau, S.; Glaus, M.; Jacquier, P.; Kupcik, T.; Maes, N.; Montoya, V.; Rabung, T.; Robinet, J.-C.; Savoye, S.; Schaefer, T.; Tournassat, C.; Van Laer, L.; Van Loon, L.

2015-07-01

In the framework of the feasibility studies on the radioactive waste disposal in deep argillaceous formations, it is now well established that the transport properties of solutes in clay rocks, i.e. parameter values for Fick's law, are mainly governed by the negatively charged clay mineral surface. While a good understanding of the diffusive behaviour of non-reactive anionic and neutral species is now achieved, much effort has to be placed on improving understanding of coupled sorption/diffusion phenomena for sorbing cations. Indeed, several cations known to form highly stable surface complexes with sites on mineral surfaces migrate more deeply into clay rock than expected. Therefore, the overall objective of the EC CatClay project is to address this issue, using a 'bottom-up' approach, in which simpler, analogous systems (here a compacted clay, 'pure' illite) are experimentally studied and modelled, and then the transferability of these results to more complex materials, i.e. the clay rocks under consideration in France, Switzerland and Belgium for hosting radioactive waste disposal facilities, is verified. The cations of interest were chosen for covering a representative range of cations families: from a moderately sorbing cation, the strontium, to three strongly sorbing cations, Co(II), Zn(II) and Eu(III). For the 4 years of this project, much effort was devoted to developing and applying specific experimental methods needed for acquiring the high precision, reliable data needed to test the alternative hypotheses represented by different conceptual-numerical models. The enhanced diffusion of the sorbing cations of interest was confirmed both in the simpler analogous illite system for Sr 2+ , Co(II) and Zn(II), but also in the natural clay rocks, except for Eu(III). First modelling approach including diffusion in the diffuse double layer (DDL) promisingly succeeded in reproducing the experimental data under the various conditions both in

Comparing uranyl sorption complexes on soil and reference clays

International Nuclear Information System (INIS)

Chisholm-Brause, C.J.; Berg, J.M.; Conradson, S.D.; Morris, D.E.; McKinley, J.P.; Zachara, J.M.

1993-01-01

Clay minerals and other components in natural soils may play a key role in limiting the mobility of uranium in the environment through the formation of sorption complexes. Reference clays are frequently used as models to study sorption processes because they have well-known chemical and physical properties, but they may differ chemically and morphologically from clays derived from natural soils. Therefore, inferences based on reference clay data have been questioned. The authors have used luminescence and x-ray absorption spectroscopies to characterize the sorption complexes of aqueous uranyl (UO 2 2+ ) species on two soil smectites from the Kenoma and Ringold formations, and compared these results to those obtained on reference smectite clays. The pH dependence of uptake suggests that the ratio of sorption on amphoteric edge sites is greater for the soil smectites than for reference clays such as Wyoming montmorillonite (SWy-1). The luminescence spectra for uranyl sorbed to the soil clays are very similar to those for uranyl sorbed principally to the edge sites of SWy-1. This observation supports the solution data suggesting that adsorption to amphoteric sites is a more important mechanism for soil clays. However, the spectral data indicate that the sorption complexes on natural and reference clays are quite similar. Furthermore, as with the reference clays, the authors have found that the chemistry of the solution plays a greater role in defining the sorption complex than does the clay matrix. Thus, if differences in surface properties are adequately taken into account, the reference clays may serve as useful analogs for soil clays in investigations of metal-ion sorption

Numerical Analysis of Diaphragm Wall Model Executed in Poznań Clay Formation Applying Selected Fem Codes

Directory of Open Access Journals (Sweden)

Superczyńska M.

2016-09-01

Full Text Available The paper presents results of numerical calculations of a diaphragm wall model executed in Poznań clay formation. Two selected FEM codes were applied, Plaxis and Abaqus. Geological description of Poznań clay formation in Poland as well as geotechnical conditions on construction site in Warsaw city area were presented. The constitutive models of clay implemented both in Plaxis and Abaqus were discussed. The parameters of the Poznań clay constitutive models were assumed based on authors’ experimental tests. The results of numerical analysis were compared taking into account the measured values of horizontal displacements.

Clay-Alcohol-Water Dispersions: Anomalous Viscosity Changes Due to Network Formation of Clay Nanosheets Induced by Alcohol Clustering.

Science.gov (United States)

Kimura, Yuji; Haraguchi, Kazutoshi

2017-05-16

Clay-alcohol-water ternary dispersions were compared with alcohol-water binary mixtures in terms of viscosity and optical absorbance. Aqueous clay dispersions to which lower alcohols (ethanol, 1-propanol, 2-propanol, and tert-butanol) were added exhibited significant viscosity anomalies (maxima) when the alcohol content was 30-55 wt %, as well as optical absorbance anomalies (maxima). The maximum viscosity (η max ) depended strongly on the clay content and varied between 300 and 8000 mPa·s, making it remarkably high compared with the viscosity anomalies (2 mPa·s) observed in alcohol-water binary mixtures. The alcohol content at η max decreased as the hydrophobicity of the alcohol increased. The ternary dispersions with viscosity anomalies exhibited thixotropic behaviors. The effects of other hydrophilic solvents (glycols) and other kinds of clays were also clarified. Based on these findings and the average particle size changes, the viscosity anomalies in the ternary dispersions were explained by alcohol-clustering-induced network formation of the clay nanosheets. It was estimated that 0.9, 1.7, and 2.5 H 2 O molecules per alcohol molecule were required to stabilize the ethanol, 2-propanol, and tert-butanol, respectively, in the clay-alcohol-water dispersions.

Influence of clay mineralogy on clay based ceramic products

International Nuclear Information System (INIS)

Radzali Othman; Tuan Besar Tuan Sarif; Zainal Arifin Ahmad; Ahmad Fauzi Mohd Noor; Abu Bakar Aramjat

1996-01-01

Clay-based ceramic products can either be produced directly from a suitable clay source without the need further addition or such products can be produced from a ceramic body formulated by additions of other raw materials such as feldspar and silica sand. In either case, the mineralogical make-up of the clay component plays a dominating role in the fabrication and properties of the ceramic product. This study was sparked off by a peculiar result observed in one of five local ball clay samples that were used to reformulate a ceramic body. Initial characterisation tests conducted on the clays indicated that these clays can be classified as kaolinitic. However, one of these clays produced a ceramic body that is distinctively different in terms of whiteness, smoothness and density as compared to the other four clays. Careful re-examination of other characterisation data, such as particle size distribution and chemical analysis, failed to offer any plausible explanation. Consequently, the mineralogical analysis by x-ray diffraction was repeated by paying meticulous attention to specimen preparation. Diffraction data for the clay with anomalous behaviour indicated the presence of a ∼ 10A peak that diminished when the same specimen was re-tested after heating in an oven at 12O degree C whilst the other four clays only exhibit the characteristic kaolinite (Al sub 2 O sub 3. 2SiO sub 2. 2H sub 2 0) and muscovite peaks at ∼ 7A and ∼ 10A before and after heat treatment. This suggests the presence of the mineral halloysite (A1 sub 2 0 sub 3. 2SiO sub 2.4H sub 2 0) in that particular clay. This difference in mineralogy can be attributed to account for the variations in physical properties of the final product. Consequently, this paper reviews in general the precautionary measures that must be adhered to during any mineralogical investigation of clay minerals or clay-based materials. The common pitfalls during specimen preparation, machine settings and interpretation of

Clay mineral assemblages of terrestrial records (Xining Basin, China) during the Eocene-Oligocene climate Transition (EOT) and its environmental implications

Science.gov (United States)

Zhang, C.; Guo, Z.

2013-12-01

The Eocene-Oligocene Transition (EOT) between ~34.0 and 33.5 million years ago, where global climate cooled from 'greenhouse' to 'icehouse' at ~33.5 Ma ago, is one of the great events during Cenozoic climate deterioration. In contrast to the marine records of the EOT, significantly less research has focused on the continental climate change during this time, particularly in inner Asia. We present a comprehensive study of the upper Eocene to lower Oligocene succession with regular alternations of laterally continuous gypsum/gypsiferous layers and red mudstone beds in Tashan section of Xining Basin, which is located at the northeastern margin of the Tibetan Plateau. Clay minerals, which were extracted from this succession, were analyzed qualitatively and semi-quantitatively by using X-ray differaction (XRD). Base on detailed magnetostratigraphic time control, clay mineral compositions of this succession (33.1-35.5 Ma) are compared with open ocean marine records and Northern Hemisphere continental records to understand the process and characteristics of Asian climate change before, during and after EOT. Our results indicate that illite is the dominant clay mineral with less chlorite and variable smectite. Multi-parameter evidence suggests that the source areas of detrital inputs in Tashan have not changed and climate is the main control for the composition of the clay fraction. The characteristics of clay mineral concentrations suggest warm and humid fluctuations with cold and dry conditions and intense of seasonality during ~35.5-34.0 Ma in inner Asian. This changed to cold and dry condition at ~34 Ma and remained so from ~34-33.1 Ma. The comparisons between continental and marine records indicate that the climate changes experienced in the Xining basin region are more consistent with Northern Hemisphere rather than open oceans records. This indicates that paleoclimate changes for inner Asian before, during and after EOT was not controlled by Antarctic ice growth

Physicochemical Properties, Micromorphology and Clay Mineralogy of Soils Affected by Geological Formations, Geomorphology and Climate

Directory of Open Access Journals (Sweden)

A. Bayat

2017-01-01

Neogene conglomerates are among dominant geological formations of piedmont plain. Eleven pedons affected by young Quaternary sediments, Neogene and Cretaceous marls in aridic, aridic border to xeric, and xeric moisture regimes on above-mentioned geomorphic surfaces were described and sampled using Natural Resources Conservation Service (2012 guideline. Physicochemical properties, clay mineralogy, and micromorphology of soil samples investigated and soils were classified by Soil Taxonomy (2014 and WRB (2015 systems. Results and Discussion: Calcic, gypsic, argillic, and cambic diagnostic horizons investigated after field and laboratory studies. Typic Calcigypsids, Lithic Torriorthents, Typic Haplogypsids, Typic Haplocalcids, Typic Torrifluvents, Sodic Haplocambids, Typic Calciargids, and Xeric Haplocalcids subgroups were found using Soil Taxonomy (2014 system. Gypsisols, Calcisols, Luvisols, Cambisols, and Regosols reference soil groups identified by WRB (2015 classification system. Developed Alfisols, formed on piedmont plain geomorphic surface in xeric moisture regime. On the other hand, Entisols formed on rock pediments with aridic moisture regime. Soils in aridic moisture regimes were little developed with gypsic horizon, and where calcic horizon was formed, it was near the surface. Moving to the west with increasing humidity, gypsum was leached from the pedon and clay illuviation caused argillic horizon to be formed. Formation of Btk horizon in pedon 9 was attributed to a more paleoclimate. The maximum gypsum content of 44.7 % (gypsiferous soils was found in soils affected by Quaternary formations and Cretaceous marls, but the maximum calcium carbonate (44 %, calcareous soils was investigated in soils formed on Neogene conglomerate formations. Moreover, the maximum sodium adsorption ratio (SAR content (29.2 (mmol(± L-10.5 was determined for soils on unstable surface of alluvial plain. Smectite, vermiculite, illite, kaolinite, and chlorite clay minerals were

Microbial reduction of structural iron in interstratified illite-smectite minerals by a sulfate-reducing bacterium.

Science.gov (United States)

Liu, D; Dong, H; Bishop, M E; Zhang, J; Wang, H; Xie, S; Wang, S; Huang, L; Eberl, D D

2012-03-01

Clay minerals are ubiquitous in soils, sediments, and sedimentary rocks and could coexist with sulfate-reducing bacteria (SRB) in anoxic environments, however, the interactions of clay minerals and SRB are not well understood. The objective of this study was to understand the reduction rate and capacity of structural Fe(III) in dioctahedral clay minerals by a mesophilic SRB, Desulfovibrio vulgaris and the potential role in catalyzing smectite illitization. Bioreduction experiments were performed in batch systems, where four different clay minerals (nontronite NAu-2, mixed-layer illite-smectite RAr-1 and ISCz-1, and illite IMt-1) were exposed to D. vulgaris in a non-growth medium with and without anthraquinone-2,6-disulfonate (AQDS) and sulfate. Our results demonstrated that D. vulgaris was able to reduce structural Fe(III) in these clay minerals, and AQDS enhanced the reduction rate and extent. In the presence of AQDS, sulfate had little effect on Fe(III) bioreduction. In the absence of AQDS, sulfate increased the reduction rate and capacity, suggesting that sulfide produced during sulfate reduction reacted with the phyllosilicate Fe(III). The extent of bioreduction of structural Fe(III) in the clay minerals was positively correlated with the percentage of smectite and mineral surface area of these minerals. X-ray diffraction, and scanning and transmission electron microscopy results confirmed formation of illite after bioreduction. These data collectively showed that D. vulgaris could promote smectite illitization through reduction of structural Fe(III) in clay minerals. © 2011 Blackwell Publishing Ltd.

Effects of hydrogen peroxide pretreatment of clay minerals on the adsorption of Sr-85 and Tc-95m under anoxic conditions

International Nuclear Information System (INIS)

Relyea, J.F.; Washburne, C.D.

1979-01-01

Treatment of three clay minerals with hydrogen peroxide affects the observed adsorption behavior of technetium relative to untreated clay under anoxic conditions. A possible adsorption mechanism of Tc is the reduction of TcO - 4 to a more positively charged or better adsorbed species. Oxidation of the clay by H 2 O 2 would hinder the reduction of TcO - 4 by buffering the clay-water system at a higher Eh value, although a difference in measured Eh value may go undetected. Sorption of strontium by the clays under the same conditions is not affected by a pretreatment with H 2 O 2 . The behavior of strontium follows that expected from ion exchange theory. 13 tables

Clay minerals related to the circulation of geothermal fluids in boreholes at Rittershoffen (Alsace, France)

Science.gov (United States)

Vidal, Jeanne; Patrier, Patricia; Genter, Albert; Beaufort, Daniel; Dezayes, Chrystel; Glaas, Carole; Lerouge, Catherine; Sanjuan, Bernard

2018-01-01

Two geothermal wells, GRT-1 and GRT-2, were drilled into the granite at Rittershoffen (Alsace, France) in the Upper Rhine Graben to exploit geothermal resources at the sediment-basement interface. Brine circulation occurs in a permeable fracture network and leads to hydrothermal alteration of the host rocks. The goal of the study was to characterize the petrography and mineralogy of the altered rocks with respect to the permeable fracture zones in the granitic basement. As clay minerals are highly reactive to hydrothermal alteration, they can be used as indicators of present-day and paleo-circulation systems. Special attention has been paid to the textural, structural and chemical properties of these minerals. The fine-grained clay fraction (smectite ( 10% smectite) provide a promising guide for identifying the fracture zones that control the present-day circulation of geothermal fluids in the Rittershoffen wells. However, multistage paleo-circulation systems could lead to an abundance of heterogeneous and fine-grained illitic minerals that could plug the fracture system. The permeability of fracture zones in the GRT-1 well was likely reduced because of an intense illitization, and the well was stimulated. The occurrence of chlorite in the permeable fracture zones of GRT-2 is indicative of less intense illitization, and the natural permeability is much higher in GRT-2 than in GRT-1.

Hydro-mechanical properties of the red salt clay (T4) - Natural analogue of a clay barrier

International Nuclear Information System (INIS)

Minkley, W.; Popp, T.; Salzer, K.; Gruner, M.; Boettge, V.

2010-01-01

Document available in extended abstract form only. Long-term storage of high-level radioactive waste in deep geologic formations is worldwide the only accepted solution to warranty long term safety. Besides clay and crystalline rocks, salt is one of the potential host-rock candidates, mainly favored in Germany. As salts rocks are highly soluble their barrier integrity against water inflow from the cap rock is questionable. Argillaceous cap rocks or intercalated clay layers may act as protective shield in the hanging wall above a repository, thus providing a multi-barrier system. The aims of our study are twofold: 1) to characterize the mineralogical, hydraulic and rock-mechanical properties of the so-called Red Salt Clay (T4) as natural analogue of a clay barriers represented by different states of induration corresponding to various depth of burial diagenesis; 2) to demonstrate the favoured barrier properties of an argillaceous layer in the top of a salt formation undergoing dynamic processes such as rock bursts. The so-called Red Salt Clay (T4) is deposited as clay rich clastic sediment at the base of the Aller-series forming a persistent lateral layer above the lower Zechstein-series. The thickness of the clay-formation becomes smaller with decreasing distance from the border of the basin, i.e. from ∼15 m at Rossleben, over 7 m at Bernburg to 3.5 m at Zielitz, all in Saxony-Anhalt, D). The mineralogical composition of the Red Salt Clay varies, e.g. average composition for the Teutschenthal area: clay minerals 54% (Chlorite: 8%; Illite/Muscovite: 46%); quartz: 22%; anhydrite: 15%; accessory gypsum; Halite: 6%, Hematite: ∼ 2%). The geochemical and mineralogical composition of the Red Salt Clay represents a final state of natural salt-clay-systems, thus standing as a natural analogue for bentonite-based sealing systems in contact with high-saline solutions (e.g. saturated NaCl-solution, solutions with various Mg 2+ -, K + -, SO 4 2- - concentrations). The

Iodide Sorption to Clays and the Relationship to Surface Charge and Clay Texture - 12356

Energy Technology Data Exchange (ETDEWEB)

Miller, Andrew; Kruichiak, Jessica; Tellez, Hernesto; Wang, Yifeng [Sandia National Laboratories, Albuquerque, NM 87185 (United States)

2012-07-01

Iodine is assumed to behave conservatively in clay barriers around nuclear waste repositories and in natural sediments. Batch experiments tend to show little to no sorption, while in column experiments iodine is often retarded relative to tritiated water. Current surface complexation theory cannot account for negatively charged ion sorption to a negatively charged clay particle. Surface protonation and iodide sorption to clay minerals were examined using surface titrations and batch sorption experiments with a suite of clay minerals. Surface titrations were completed spanning a range of both pH values and ionic strengths. For reference, similar titrations were performed on pure forms of an Al-O powder. The titration curves were deconvoluted to attain the pKa distribution for each material at each ionic strength. The pKa distribution for the Al-O shows two distinct peaks at 4.8 and 7.5, which are invariant with ionic strength. The pKa distribution of clays was highly variable between the different minerals and as a function of ionic strength. Iodide sorption experiments were completed at high solid:solution ratios to exacerbate sorption properties. Palygorskite and kaolinite had the highest amount of iodide sorption and montmorillonite had the least. (authors)

Formation and Stabilization of Environmentally Persistent Free Radicals Induced by the Interaction of Anthracene with Fe(III)-Modified Clays.

Science.gov (United States)

Jia, Hanzhong; Nulaji, Gulimire; Gao, Hongwei; Wang, Fu; Zhu, Yunqing; Wang, Chuanyi

2016-06-21

Environmentally persistent free radicals (EPFRs) are occasionally detected in Superfund sites but the formation of EPFRs induced by polycyclic aromatic hydrocarbons (PAHs) is not well understood. In the present work, the formation of EPFRs on anthracene-contaminated clay minerals was quantitatively monitored via electron paramagnetic resonance (EPR) spectroscopy, and surface/interface-related environmental influential factors were systematically explored. The obtained results suggest that EPFRs are more readily formed on anthracene-contaminated Fe(III)-montmorillonite than in other tested systems. Depending on the reaction condition, more than one type of organic radicals including anthracene-based radical cations with g-factors of 2.0028-2.0030 and oxygenic carbon-centered radicals featured by g-factors of 2.0032-2.0038 were identified. The formed EPFRs are stabilized by their interaction with interlayer surfaces, and such surface-bound EPFRs exhibit slow decay with 1/e-lifetime of 38.46 days. Transformation pathway and possible mechanism are proposed on the basis of experimental results and quantum mechanical simulations. Overall, the formation of EPFRs involves single-electron-transfer from anthracene to Fe(III) initially, followed by H2O addition on formed aromatic radical cation. Because of their potential exposure in soil and atmosphere, such clay surface-associated EPFRs might induce more serious toxicity than PAHs and exerts significant impacts on human health.

Mineral-produced high-pressure striae and clay polish: Key evidence for nonballistic transport of ejecta from Ries crater

Science.gov (United States)

Chao, E.C.T.

1976-01-01

Recently discovered mineral-produced, deeply incised striae and mirror-like polish on broken surfaces of limestone fragments from the sedimentary ejecta of the Ries impact crater of southern Germany are described. The striae and polish were produced under high confining pressures during high-velocity nonballistic transport of the ejecta mass within the time span of the cratering event (measured in terms of seconds). The striae on these fragments were produced by scouring by small mineral grains embedded in the surrounding clay matrix, and the polish was formed under the same condition, by movements of relatively fragment-free clay against the fragment surfaces. The occurrence of these striae and polish is key evidence for estimating the distribution and determining the relative importance of nonballistic and ballistic transport of ejecta from the shallow Ries stony meteorite impact crater.

Coupling diffusion and high-pH precipitation/dissolution in the near field of a HLW repository in clay by means of reactive solute transport models

Science.gov (United States)

Samper, J.; Font, I.; Yang, C.; Montenegro, L.

2004-12-01

The reference concept for a HLW repository in clay in Spain includes a 75 cm thick bentonite buffer which surrounds canisters. A concrete sustainment 20 cm thick is foreseen between the bentonite buffer and the clay formation. The long term geochemical evolution of the near field is affected by a high-pH hyperalkaline plume induced by concrete. Numerical models of multicomponent reactive transport have been developped in order to quantify the evolution of the system over 1 Ma. Water flow is negligible once the bentonite buffer is saturated after about 20 years. Therefore, solute transport occurs mainly by diffusion. Models account for aqueous complexation, acid-base and redox reactions, cation exchange, and mineral dissolution precipitation in the bentonite, the concrete and the clay formation. Numerical results obtained witth CORE2D indicate that the high-pH plume causes significant changes in porewater chemistry both in the bentonite buffer and the clay formation. Porosity changes caused by mineral dissolution/precipitation are extremely important. Therefore, coupled modes of diffusion and reactive transport accounting for changes in porosity caused by mineral precipitation are required in order to obtain realistic predictions.

Coupled transport phenomena in a clay from a Callovo-Oxfordian formation

International Nuclear Information System (INIS)

Paszkuta, M.

2005-06-01

Low permeability materials containing clay play an important role in practical life and natural environment. Indeed, the ability of clay soils to act as semi permeable membranes, that inhibit the passage of electrolytes, is of great interest. The major objective of this thesis is to evaluate the transport properties of natural clays and in particular coupled transports when a pressure gradient, an electrical field, a concentration gradient and a temperature gradient interact. The material is a compact argillite extracted in East France from a Callovo-Oxfordian formation which was supplied to us by ANDRA. NaCl was used as the main solute. Two series of experiments were performed to measure permeability, diffusion, conductivity, the electro-osmotic coefficient and the Soret coefficient. (author)

Stepwise effects of the BCR sequential chemical extraction procedure on dissolution and metal release from common ferromagnesian clay minerals: A combined solution chemistry and X-ray powder diffraction study

Energy Technology Data Exchange (ETDEWEB)

Ryan, P.C. [Geology Department, Middlebury College, Middlebury, Vermont 05753 (United States)], E-mail: pryan@middlebury.edu; Hillier, S. [Macaulay Institute, Aberdeen, AB15 8QH UK (United Kingdom); Wall, A.J. [Department of Geosciences, Penn State University, University Park, Pennsylvania, 16802 (United States)

2008-12-15

Sequential extraction procedures (SEPs) are commonly used to determine speciation of trace metals in soils and sediments. However, the non-selectivity of reagents for targeted phases has remained a lingering concern. Furthermore, potentially reactive phases such as phyllosilicate clay minerals often contain trace metals in structural sites, and their reactivity has not been quantified. Accordingly, the objective of this study is to analyze the behavior of trace metal-bearing clay minerals exposed to the revised BCR 3-step plus aqua regia SEP. Mineral quantification based on stoichiometric analysis and quantitative powder X-ray diffraction (XRD) documents progressive dissolution of chlorite (CCa-2 ripidolite) and two varieties of smectite (SapCa-2 saponite and SWa-1 nontronite) during steps 1-3 of the BCR procedure. In total, 8 ({+-} 1) % of ripidolite, 19 ({+-} 1) % of saponite, and 19 ({+-} 3) % of nontronite (% mineral mass) dissolved during extractions assumed by many researchers to release trace metals from exchange sites, carbonates, hydroxides, sulfides and organic matter. For all three reference clays, release of Ni into solution is correlated with clay dissolution. Hydrolysis of relatively weak Mg-O bonds (362 kJ/mol) during all stages, reduction of Fe(III) during hydroxylamine hydrochloride extraction and oxidation of Fe(II) during hydrogen peroxide extraction are the main reasons for clay mineral dissolution. These findings underscore the need for precise mineral quantification when using SEPs to understand the origin/partitioning of trace metals with solid phases.

Heteroagglomeration of zinc oxide nanoparticles with clay mineral modulates the bioavailability and toxicity of nanoparticle in Tetrahymena pyriformis.

Science.gov (United States)

Gupta, Govind Sharan; Senapati, Violet Aileen; Dhawan, Alok; Shanker, Rishi

2017-06-01

The extensive use of zinc oxide nanoparticles (ZnO NPs) in cosmetics, sunscreens and healthcare products increases their release in the aquatic environment. The present study explored the possible interaction of ZnO NPs with montmorillonite clay minerals in aqueous conditions. An addition of ZnO NPs on clay suspension significantly (pclay particles from 1652±90nm to 2158±13nm due to heteroagglomeration. The electrokinetic measurements showed a significant (pclay association (-1.37±0.03μmcm/Vs) that results to the electrostatic interaction between ZnO NPs and clay particles. The attenuated total reflectance Fourier transform infrared spectroscopy analysis of ZnO NPs-clay association demonstrated the binding of ZnO NPs with the Si-O-Al region on the edges of clay particles. The increase in size of ZnO NPs-clay heteroagglomerates further leads to their sedimentation at 24h. Although, the stability of ZnO NPs in the clay suspension was decreased due to heteroagglomeration, but the bioavailability and toxicity of ZnO NPs-clay heteroagglomerates in Tetrahymena pyriformis was enhanced. These observations provide an evidence on possible mechanisms available in natural environment that can facilitate nanoparticles entry into the organisms present in lower trophic levels of the food web. Copyright © 2017 Elsevier Inc. All rights reserved.

Mild acid and alkali treated clay minerals enhance bioremediation of polycyclic aromatic hydrocarbons in long-term contaminated soil: A 14C-tracer study.

Science.gov (United States)

Biswas, Bhabananda; Sarkar, Binoy; Rusmin, Ruhaida; Naidu, Ravi

2017-04-01

Bioremediation of polycyclic aromatic hydrocarbon (PAH)-contaminated soils requires a higher microbial viability and an increased PAH bioavailability. The clay/modified clay-modulated bacterial degradation could deliver a more efficient removal of PAHs in soils depending on the bioavailability of the compounds. In this study, we modified clay minerals (smectite and palygorskite) with mild acid (HCl) and alkali (NaOH) treatments (0.5-3 M), which increased the surface area and pore volume of the products, and removed the impurities without collapsing the crystalline structure of clay minerals. In soil incubation studies, supplements with the clay products increased bacterial growth in the order: 0.5 M HCl ≥ unmodified ≥ 0.5 M NaOH ≥ 3 M NaOH ≥ 3 M HCl for smectite, and 0.5 M HCl ≥ 3 M NaOH ≥ 0.5 M NaOH ≥ 3 M HCl ≥ unmodified for palygorskite. A 14 C-tracing study showed that the mild acid/alkali-treated clay products increased the PAH biodegradation (5-8%) in the order of 0.5 M HCl ≥ unmodified > 3 M NaOH ≥ 0.5 M NaOH for smectite, and 0.5 M HCl > 0.5 M NaOH ≥ unmodified ≥ 3 M NaOH for palygorskite. The biodegradation was correlated (r = 0.81) with the bioavailable fraction of PAHs and microbial growth as affected particularly by the 0.5 M HCl and 0.5 M NaOH-treated clay minerals. These results could be pivotal in developing a clay-modulated bioremediation technology for cleaning up PAH-contaminated soils and sediments in the field. Copyright © 2017 Elsevier Ltd. All rights reserved.

Self-sealing of fractures in argillaceous formations - Evidence, mechanisms and implications for performance assesment (an NEA Clay Club project)

International Nuclear Information System (INIS)

Bock, H.; Dehandschutter, B.; Martin, C.D.; Mazurek, M.; Haller, A. de; Skoczylas, F.; Davy, C.

2010-01-01

of veins and in the sealing of hard fissile clay-stones. Relating to a time scale of the order of 100 years, evidence for self-sealing of natural and induced fractures has been found in old traffic tunnels. Numerous laboratory and URL experiments have shown that, in soft and moderately indurated formations, self-sealing commonly occurs within a time span of months up to a few years. The project has advanced the knowledge on the general geo-conditions (G) (geologic, hydrogeological, geochemical, geotechnical) which must prevail in deep geological repositories that argillaceous formations become amenable to self-sealing. The following seven sealing mechanisms (M) were considered on their respective sealing potential of argillaceous formations in repository conditions: - M-1 Sealing of rock matrix by additional compaction (porosity reduction) - M-2 Closure of fractures by increased effective normal stress sn' - M-3 Contraction of fractures when subjected to shear - M-4 Creep of the fracture wall material towards the open fracture space - M-5 Swelling of the fracture wall material - M-6 Slaking of the fracture wall material (both body and surface slaking) - M-7 Mineral precipitation onto fracture walls. With regard to PA relevance, each self-sealing issue was finally classified in line with a scheme developed within the FEPCAT approach. It is concluded that the scientific knowledge on self-sealing has progressed to a level which, for soft and slight to moderately indurated argillaceous formations, could justify the inclusion of sealing processes in the performance assessment (PA) of deep geological repositories. (authors)

Adsorption of zinc and lead on clay minerals

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Katarína Jablonovská

2006-12-01

Full Text Available Clays (especially bentonite, zeolite and quartz sand are widely used as landfill barriers to prevent contamination of subsoil and groundwater by leachates containing heavy metals. The sorption of zinc and lead on these clays was studied as a function of time and it was found that the initial 1 h our was sufficient to exchange most of the metal ions. The retention efficiency of clay samples of Zn2+ and Pb2+ follows the order of bentonite > zeolite> quartz sand. Whatever the clay sample, lead is retained more than zinc. The concentration of elements in the solution was followed by atomic adsorption spectrofotometry. Bacillus cereus and Bacillus pumilus, previously isolated from the kaoline deposit Horna Prievrana was added into the clay samples to comparise the accumulation of Zn2+ and Pb2+ from the model solution. The study of heavy metal adsorption capacity of bacteria- enriched clay adsorbent showed a high retention efficiency for lead ions as comparised with zinc ions. Biosorption is considered a potential instrument for the removal of metals from waste solutions and for the precious metals recovery as an alternative to the conventional processes.

Mode of distribution of uranium mineralization and sequence of the formation of minerals in albitites

International Nuclear Information System (INIS)

Grechishnikov, N.P.; Kramar, O.A.; Rapovich, F.I.

1985-01-01

On the basis of analysis and generalization of factural material data on the distribution nature of accessory uranium mineralization in albitites permitting to judge of the role and textural-structural peculiarities of enclosing rocks in mineralization localization are given. It is shown that the uranium mineral formation is closely related with the albitite formation and proceeded during two stages. A main mass of primary uranium minerals (brannerites and uraninites) in the form of impregnated mineralization was formed during the first uraninite-brannerite-albitite stage. Uranium oxides, silicates and titanates in the shape of veines formed. During the second coffinite-pitchblende-chloritic stage the formation of uranium oxides, silicates and titanates occured. Uranium mineralization in albitites developes in zones of cataclasm, small jointing, mylonitization localizing in fine-grained aggregates. A main mass of primary uranium minerals in albitites (brannerite, uraninite relates to neogenic during metasomatosis dark-coloured minerals (riebenite, aegirine, chlorite)

Clay Mineralogy of Coal-Hosted Nb-Zr-REE-Ga Mineralized Beds from Late Permian Strata, Eastern Yunnan, SW China: Implications for Paleotemperature and Origin of the Micro-Quartz

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Lixin Zhao

2016-05-01

Full Text Available The clay mineralogy of pyroclastic Nb(Ta-Zr(Hf-REE-Ga mineralization in Late Permian coal-bearing strata from eastern Yunnan Province; southwest China was investigated in this study. Samples from XW and LK drill holes in this area were analyzed using XRD (X-ray diffraction and SEM (scanning electronic microscope. Results show that clay minerals in the Nb-Zr-REE-Ga mineralized samples are composed of mixed layer illite/smectite (I/S; kaolinite and berthierine. I/S is the major component among the clay assemblages. The source volcanic ashes controlled the modes of occurrence of the clay minerals. Volcanic ash-originated kaolinite and berthierine occur as vermicular and angular particles, respectively. I/S is confined to the matrix and is derived from illitization of smectite which was derived from the original volcanic ashes. Other types of clay minerals including I/S and berthierine precipitated from hydrothermal solutions were found within plant cells; and coexisting with angular berthierine and vermicular kaolinite. Inferred from the fact that most of the I/S is R1 ordered with one case of the R3 I/S; the paleo-diagenetic temperature could be up to 180 °C but mostly 100–160 °C. The micro-crystalline quartz grains (<10 µm closely associated with I/S were observed under SEM and were most likely the product of desiliconization during illitization of smectite.

Common clay and shale

Science.gov (United States)

Virta, R.L.

2000-01-01

Part of the 1999 Industrial Minerals Review. The clay and shale market in 1999 is reviewed. In the U.S., sales or use of clay and shale increased from 26.4 million st in 1998 to 27.3 million st in 1999, with an estimated 1999 value of production of $143 million. These materials were used to produce structural clay products, lightweight aggregates, cement, and ceramics and refractories. Production statistics for clays and shales and for their uses in 1999 are presented.

Laboratory experiments on ammoniated clay minerals with relevance for asteroid (1) Ceres

Science.gov (United States)

De Angelis, Simone; Stefani, Stefania; De Sanctis, Maria Cristina; Piccioni, Giuseppe; Ammannito, Eleonora

2017-04-01

Recent observations with VIR spectrometer onboard Dawn spacecraft [1] have suggested the presence of ammoniated phyllosilicates widespread on the surface of asteroid (1) Ceres [2,3]. The global surface composition of Ceres as suggested by VIR average infrared spectrum in the 1-4 micron range appears to be due to a mixture of NH4-bearing phyllosilicates, serpentine, carbonates and a dark absorbing phase (magnetite or amorphous carbon) [2]. An absorption feature occurring near 3.1 micron in the average spectrum is considered the main evidence for the presence of NH4-bearing phase; nevertheless in the past several authors tried to explain this feature, as observed with telescopic spectra, invoking the presence of brucite, cronstedtite, water ice or clays [4]. In this project we are carrying out laboratory experiments with the aim of studying ammoniated phyllosilicates in the visible-infrared range. A suite of 9 clay minerals has been used for this study, including illite, nontronite and montmorillonite. In order to produce the ammoniated species we followed a modified procedure based on the one described in Bishop et al. (2002) [5]. All minerals were reduced in fine grain size (features, appearing at different wavelengths near 2, 3, 6 and 7 micron. In some cases the spectral shape of already existent absorption bands resulted deeply modified. A few species did not show the appearance of new features. These results suggest that NH4+ ions fix in various ways in different minerals. Nontronite and montmorillonite appear to be the best candidates, among the studied suite, to be used in future laboratory reproduced analog mixtures. [1] Russell C.T. et al., 2004, Planetary and Space Science, 52, 465-489 [2] De Sanctis M.C. et al., 2015, Nature, 528, 241-244 [3] Ammannito E. et al., 2016, Science, vol.353, issue 6303 [4] Rivkin A.S. et al., 2011, Space Science Reviews, 163, 95-116 [5] Bishop J.L. et al., 2002, Planetary and Space Science, 50, 11-19

[Rapid determination of major and trace elements in the salt lake clay minerals by X-ray fluorescence spectrometry].

Science.gov (United States)

Wang, Xiao-Huan; Meng, Qing-Fen; Dong, Ya-Ping; Chen, Mei-Da; Li, Wu

2010-03-01

A rapid multi-element analysis method for clay mineral samples was described. This method utilized a polarized wave-length dispersive X-ray fluorescence spectrometer--Axios PW4400, which had a maximum tube power of 4 000 watts. The method was developed for the determination of As, Mn, Co, Cu, Cr, Dy, Ga, Mo, P, Pb, Rb, S, Sr, Ni, ,Cs, Ta, Th, Ti, U, V, Y, Zn, Zr, MgO, K2O, Na2O, CaO, Fe2O3, Al2O3, SiO2 and so on. Thirty elements in clay mineral species were measured by X-ray fluorescence spectrometry with pressed powder pellets. Spectral interferences, in particular the indirect interferences of each element, were studied. A method to distinguish the interference between each other periodic elements in element periodic table was put forward. The measuring conditions and existence were mainly investigated, and the selected background position as well as corrected spectral overlap for the trace elements were also discussed. It was found that the indirect spectral overlap line was the same important as direct spectral overlap line. Due to inducing the effect of indirect spectral overlap, some elements jlike Bi, Sn, W which do not need analysis were also added to the elements channel. The relative standard deviation (RSD) was in the range of 0.01% to 5.45% except three elements Mo, Cs and Ta. The detection limits, precisions and accuracies for most elements using this method can meet the requirements of sample analysis in clay mineral species.

Characterization and technological properties of mineral clays used in the Southwest of Parana and West of Santa Catarina states

International Nuclear Information System (INIS)

Valdameri, C.Z.; Ciesca, D.F.; Zatta, L.; Anaissi, F.J.

2014-01-01

This paper aims to characterize clay minerals used in the ceramic industry in southwestern region of Parana and west of Santa Catarina states. The precursors used were the same used by industries in these regions for the production of bricks. The precursors were characterized,preliminary results are shown with respect to structural, chemical and physical precursors (XRD, EDS and plasticity). The specimens were characterized for technological burning properties: linear shrinkage, water absorption, flexural tension and density. The results show that the clays present Typical chemical composition of raw clay, however, the evaluation of technological properties after burning indicate negative results to be applied to the manufacture of red ceramic because did not meet the regulatory requirements. (author)

The nanosphere iron mineral(s) in Mars soil

Science.gov (United States)

Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

1993-01-01

A series of surface-modified clays containing nanophase (np) iron/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these 'Mars-soil analogs' were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxyl mineral such as 'green rust', or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable meaghemite (gamma-Fe203) by mild heat treatment and then to nanophase hematite (aplha-Fe203) by extensive heat treatment. Their chemical reactivity offers a plausible mechanism for the somewhat puzzling observations of the Viking biology experiments. Their unique chemical reactivities are attributed to the combined catalytic effects of the iron oxide/oxyhydroxide and silicate phase surfaces. The mode of formation of these (nanophase) iron oxides on Mars is still unknown.

Pre-treatment of Used-Cooking Oil as Feed Stocks of Biodiesel Production by Using Activated Carbon and Clay Minerals

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Rudy Syah Putra

2014-02-01

Full Text Available Many low-cost feedstock i.e. used-cooking oil (UCO for the production of biodiesel fuel (BDF has contained a large amount of water and high proportion of free fatty acids (FFAs. Therefore, a pre-treatment process to reduce the water content (<0.1 wt.% and FFAs (<2.0 wt.% were necessary in order to avoid an undesirable side reactions, such as saponification, which could lead to serious problem of product separation and low fatty acid methyl ester (FAME yield. . In this study, a pre-treatment process of used cooking oil as a feedstock for the production of BDF by using various adsorbents such as Activated Carbon (AC and various clay minerals, for example Smectite (S, Bentonite (B, Kaolinite (K, and Powdered Earthenware (PE were evaluated. The oil obtained from pre-treatment was compared with oil without pre-treatment process. In this study, we reported a basic difference in material ability to the oil, depending on the adsorption condition with respect to the physico-chemical parameters, e.g. refractive index (R, density (ρ, FFAs, and water content (W. The results showed that the water content and FFAs in the oil has decreased when using AC as an adsorbent compared with clay minerals. However, the refractive index of oil has similar with the oil without pre-treatment process as well; meanwhile, the density of oil has increased after the pre-treatment process by using clay minerals.

Aspects of clay/concrete interactions

International Nuclear Information System (INIS)

Oscarson, D.W.; Dixon, D.A.; Onofrei, M.

1997-01-01

In the Canadian concept for nuclear fuel waste management, both clay-based materials and concrete are proposed for use as barriers, seals or supporting structures. The main concern when clays and concrete are in proximity is the generation of a high-pH environment by concrete since clay minerals are relatively unstable at high pH. Here we examine the OH - -generating capacity of two high-performance concretes when in contact with several solutions. We also investigate various aspects of claylconcrete interactions. They are: (1) the alkalimetric titration of clay suspensions, (2) the effect of Ca(OH) 2 (portlandite) on the swelling and hydraulic properties of compacted bentonite, and (3) the influence of cement grout on a backfill clay retrieved from the 900-d Buffer/Container Experiment at the Underground Research Laboratory of AECL. The results indicate that although high-performance concretes establish significantly lower poresolution pH (9 to 10) than does ordinary portland cement, the pH is still somewhat higher than that of clay/groundwater systems of about pH 8. Hence, even if high-performance concrete is used in a disposal vault, the potential still exists for clay minerals to alter over long periods of time if in contact with this concrete. The data show, however, that clays have a substantial buffering capacity, and clay-based barriers can thus neutralize much of the OH - potentially released from concrete in a vault. Moreover, even after reacting for 120 d at 85 o C with up to 5 wt.% Ca(OH) 2 , compacted bentonite (dry density = 1.2 Mg/m 3 ) retains much of its swelling capacity and has a permeability low enough (hydraulic conductivity ≤ 10 -11 m/s) to ensure that molecular diffusion will be the main transport mechanism through compacted clay-based barriers. Furthermore, according to X-ray diffractometry, the clay mineral component of backfill was not altered by contact with a cement grout for 900 d in the Buffer/Container Experiment

Geochemistry of rare earths in main media of clay formation and sedimentation

International Nuclear Information System (INIS)

Bonnot-Courtois, C.

1981-01-01

This work aims i) at a better knowledge of rare earth behavior in surface conditions and ii) possible use of rare earth as a marker for argilaceous mineral genesis. Chemical properties of rare earths and geochemistry of these elements in main rocks are recalled. Rare earth behaviour during continental alteration process, experimental hydrolysis of various magmatic materials and rare earth geochemistry in argilaceous minerals in continental shelf are examined. Then some aspects of rare earth behaviour in oceans are studied: alteration of sea bed and hydrothermalism rare earth distribution in pelagic sediments red clays of deep seas and manganese nodules. In conclusion rare earth behaviour in sedimentary processes of the exogenous cycle is summarized [fr

Mineralogy and geotechnical characteristics of some pottery clay

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Mujib Olamide ADEAGBO

2016-12-01

Full Text Available The physical properties of soils, which are tremendously influenced by the active clay minerals in soil, are of great importance in geotechnical engineering. This paper investigates the clay-sized particles of the Igbara-Odo pottery clay, and compares results obtained with available data on the bulk sample, to determine their correlation and underline the dependence of the geotechnical properties of the bulk clay material on the clay-sized particles. The bulk clay sample consists of 52% sand-size particles, 21% silt and 27% clay. Analysis of the clay-sized particles and the bulk materials shows: specific gravity of 2.07 and 2.66, liquid limit of 91.0% and 33.0%, plastic limit of 27.5% and 14.3%, plasticity index of 63.5% and 18.7% and a linear shrinkage of 7.9% and 5.4%, for both clay-sized particles and bulk clay respectively. The activity value of the clay material (0.64 suggests the presence of Kaolinite and Ilite; and these were confirmed with X-Ray diffraction on the bulk sample and clay-sized particles. X-Ray diffraction patterns shows distinctive peaks which highlight the dominance of Kaolinite (with 8 peaks in the pottery clay sample for both clay-sized particles and bulk material; while traces of other clay minerals like Illite and Halloysite and rock minerals like Mica, Feldspar and Chrysotile were also found. These results suggest that the clay possesses high viability in the manufacturing of ceramics, refractory bricks, paper, fertilizer and paint. The clay material can be used as a subgrade in road construction, since it possesses low swelling characteristics.

Methane Hydrate Formation and Dissociation in the Presence of Silica Sand and Bentonite Clay

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Kumar Saw V.

2015-11-01

Full Text Available The formation and dissociation of methane hydrates in a porous media containing silica sand of different sizes and bentonite clay were studied in the presence of synthetic seawater with 3.55 wt% salinity. The phase equilibrium of methane hydrate under different experimental conditions was investigated. The effects of the particle size of silica sand as well as a mixture of bentonite clay and silica sand on methane hydrate formation and its dissociation were studied. The kinetics of hydrate formation was studied under different subcooling conditions to observe its effects on the induction time of hydrate formation. The amount of methane gas encapsulated in hydrate was computed using a real gas equation. The Clausius-Clapeyron equation is used to estimate the enthalpy of hydrate dissociation with measured phase equilibrium data.

Biogeochemical processes in a clay formation in situ experiment: Part A - Overview, experimental design and water data of an experiment in the Opalinus Clay at the Mont Terri Underground Research Laboratory, Switzerland

International Nuclear Information System (INIS)

Wersin, P.; Leupin, O.X.; Mettler, S.; Gaucher, E.C.; Maeder, U.; De Canniere, P.; Vinsot, A.; Gaebler, H.E.; Kunimaro, T.; Kiho, K.; Eichinger, L.

2011-01-01

Highlights: → The composition was affected by the complex interplay of diffusion, mineral and surface reactions. → The 13 C signals for carbon species showed significant variations which could only be partly explained. → The main cations remained remarkably constant during the experiment. → This underlines the strong buffering via cation exchange and carbonate dissolution/precipitation. - Abstract: An in situ test in the Opalinus Clay formation, termed porewater chemistry (PC) experiment, was carried out for a period of 5 years. It was based on the concept of diffusive equilibration whereby a traced water with a composition close to that expected in the formation was continuously circulated and monitored in a packed-off borehole. The main original focus was to obtain reliable data on the pH/pCO 2 conditions of the porewater, but because of unexpected microbiologically-induced redox reactions, the objective was extended to elucidate the biogeochemical processes occurring in the borehole and to understand their impact on pH/pCO 2 and porewater chemistry in the low permeability clay formation. The behaviour of the conservative tracers 2 H and Br - could be explained by diffusive dilution in the clay and moreover the results showed that diffusive equilibration between the borehole water and the formation occurred within about 3 year's time. However, the composition and pH/pCO 2 conditions differed considerably from those of the in situ porewater. Thus, pH was lower and pCO 2 was higher than indicated by complementary laboratory investigations. The noted differences are explained by microbiologically-induced redox reactions occurring in the borehole and in the interfacial wall area which were caused by an organic source released from the equipment material. The degradation of this source was accompanied by sulfate reduction and - to a lesser extent - by methane generation, which induced a high rate of acetogenic reactions corresponding to very high acetate

Metal oxides, clay minerals and charcoal determine the composition of microbial communities in matured artificial soils and their response to phenanthrene.

Science.gov (United States)

Babin, Doreen; Ding, Guo-Chun; Pronk, Geertje Johanna; Heister, Katja; Kögel-Knabner, Ingrid; Smalla, Kornelia

2013-10-01

Microbial communities in soil reside in a highly heterogeneous habitat where diverse mineral surfaces, complex organic matter and microorganisms interact with each other. This study aimed to elucidate the long-term effect of the soil mineral composition and charcoal on the microbial community composition established in matured artificial soils and their response to phenanthrene. One year after adding sterile manure to different artificial soils and inoculating microorganisms from a Cambisol, the matured soils were spiked with phenanthrene or not and incubated for another 70 days. 16S rRNA gene and internal transcribed spacer fragments amplified from total community DNA were analyzed by denaturing gradient gel electrophoresis. Metal oxides and clay minerals and to a lesser extent charcoal influenced the microbial community composition. Changes in the bacterial community composition in response to phenanthrene differed depending on the mineral composition and presence of charcoal, while no shifts in the fungal community composition were observed. The abundance of ring-hydroxylating dioxygenase genes was increased in phenanthrene-spiked soils except for charcoal-containing soils. Here we show that the formation of biogeochemical interfaces in soil is an ongoing process and that different properties present in artificial soils influenced the bacterial response to the phenanthrene spike. © 2012 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.

Substantiation of the hydrodynamic disintegration of hydraulic fluid’s mineral component of high-clay sand in precious metals placers

Directory of Open Access Journals (Sweden)

N.P. Khrunina

2018-03-01

Full Text Available General regularities and theoretical approaches determining hydroimpulsive effects on the mineral component of the hydraulic fluid are analyzed, with reference to the disintegration of high-clay sands of gold-bearing placers. Theoretical conclusions on the hydrodynamic effect on the solid component of the hydraulic fluid give insight into emerging processes in multicomponent media under hydrodynamic influences initiated by various sources of physical and mechanical influence. It is noted that the theoretical justification of the structurally complex hydrodynamic effect on the hydraulic fluid with the formation of phenomena arising from the collision of solid components with each other and obstacles includes the consideration of changes in such force characteristics as speed, pressure, flow power, and also changes in design parameters and characteristics of the environment. A conceptual approach is given to the theoretical substantiation of the disintegration of the hydraulic fluid’s mineral component using the example of the proposed installation. Calculation of economic indicators for the use of a hydrodynamic generator in comparison with processes based on known technologies has shown significant advantages of using the proposed installation, which can increase productivity and quality production indicators.

Clay fraction mineralogy of a Cambisol in Brazil

International Nuclear Information System (INIS)

Anastacio, A. S.; Fabris, J. D.; Stucki, J. W.; Coelho, F. S.; Pinto, I. V.; Viana, J. H. M.

2005-01-01

Clay minerals having a 2:1 (tetrahedral:octahedral sheet) structure may be found in strongly weathering soils only if the local pedo-climatic environment prevents them from further weathering to other minerals such as iron oxides. The clay minerals impart important chemical properties to soils, in part by virtue of changes in the redox state of iron in their crystal structures. Knowing the chemical nature of soil clays is a first step in evaluating their potential reactivity with other soil constituents and processes, such as the chemical decomposition of organic substrates to be potentially used in environmental remediation. The purpose of this work was to characterize the iron oxides and iron-bearing clay minerals from a B horizon of a Cambisol developed on tuffite in the State of Minas Gerais, Brazil, using chemical analysis, powder X-ray diffraction, Moessbauer spectroscopy, and thermal analysis. The iron oxides of this NaOH-treated clay-fraction were found to contain mainly maghemite (γFe 2 O 3 ) and superparamagnetic goethite (αFeOOH). Kaolinite (Al 2 Si 2 O 5 (OH) 4 ), smectite, and minor portions of anatase (TiO 2 ) were identified in the CBD-treated sample.

Study of Different Argillaceous Formations Performed in the Context of the FUNMIG project

Energy Technology Data Exchange (ETDEWEB)

Fernandez, A. M.; Melon, A.; Sanchez, D. M.; Gaucher, E.; Tournassat, C.; Altmann, S.C.; Vinsot, A.; Maes, N.; Craen, M. de; Leupin, O.; Wersin, P.; Astudillo, J.

2010-07-01

Argillaceous Rock Formations of low permeability have been selected in several countries as potential geological host rock for the disposal of high level radioactive wastes (HLRW). The general barrier function of the host rock is to retard and attenuate the migration of radionuclides to the biosphere, and the properties of clay minerals sustain this barrier functions. Nowadays, a number of Underground Research Laboratories (URL) have been constructed for a more in depth investigation of the indurated as well as plastic clay rock formations indifferent countries. The HADES under ground research facility (URF) was constructed at Mol (Belgium), where the Boom Clay formation is being studied as a reference host rock formation. The Opalinus Clay formation has been studied in the Mont Terri Rock Laboratory (Switzerland). The Callovo- Oxfordian clayrock is being characterised in the Meuse/Haute-Marne Site at Bure (France). The Boda Claystone is being analysed at Mecsek in Hungary. The knowledge on biogeochemical processes which affect the transport of radionuclides through the geosphere is a key parameter for the safety case of a HLRW repository, which was the aim of the EC Project FUNMIG: Fundamental Processes of Radionuclide Migration. The main factors controlling the mobility of the radionuclides are the chemistry of the pore water, the chemical reactions involving the radionuclides and the sorption processes on clay minerals. There fore, the pore water chemistry plays an important role in determining radionuclide migration characteristics in clay-rock formations. (Author)

The use of clays as sorbents and catalysts

International Nuclear Information System (INIS)

McCabe, R.W.

1998-01-01

The paper attempts to show the structural, physical and chemical properties of clay minerals relate to their laboratory, industrial and environmental uses as sorbents and catalysts. A brief review of the formulae and structures of clays and their relationship to their chemical and physical properties follows. Clay minerals are also useful in environmental protection as they can adsorb crude oils from spills and they are used, sometimes mixed into concrete, as containment barriers for radionuclides caesium 137 and strontium 90. Clay soils can also act as natural barriers to the migration of radionuclides in the environment

Characterization of karak clay from pakistan for pharmaceutical and cosmetic applications

International Nuclear Information System (INIS)

Shah, L.A.; Silva-Valenzuela, M.G.; Valenzuela-Diaz, F.R.; Sayeg, I.J.; Carvalho, F.M.S.

2012-01-01

Full text: Clay, the most important, plentiful, and low cost naturally occurring mineral, is widely used in variety of industrial application including Pharmaceutical and cosmetic. Clay is the fine grained aluminosilicate mineral which shows the property of plasticity at appropriate water content, and becomes hard upon drying. In Pakistan there are different types of clay but till now neither of them properly identified nor characterize for specific industrial application. The objective of this work is to characterize Karak clay for pharmaceutical and cosmetic applications collected from deposit located at Shagai region, District Karak, Pakistan. The clay was characterized through Xray diffractometry (XRD), X-ray Fluorescence (XRF), trace elemental Analysis, Microbiological analysis, Cation exchange capacity (CEC), pH and swelling assays according to European, United States of America and Brazilian Pharmacopeias. Bulk Chemical analysis shows that the Aluminum oxide and silica oxide are present in large quantity which was confirmed by XRD that this sample has montmorillonite as a major while illite and kaolinite as minor clay minerals. Quartz of small quantity was also found as a non-clay mineral. After analyzing the results for sample it was concluded that the clay is a strong candidate for cosmetic purposes. (author)

Litho- and biostratigraphy of the Opalinus Clay and bounding formations in the Mont Terri rock laboratory (Switzerland)

International Nuclear Information System (INIS)

Hostettler, B.; Reisdorf, A. G.; Jaeggi, D.

2017-01-01

A 250 m-deep inclined well, the Mont Terri BDB-1, was drilled through the Jurassic Opalinus Clay and its bounding formations at the Mont Terri rock laboratory (NW Switzerland). For the first time, a continuous section from (oldest to youngest) the topmost members of the Staffelegg Formation to the basal layers of the Hauptrogenstein Formation is now available in the Mont Terri area. We extensively studied the drill core for lithostratigraphy and biostratigraphy, drawing upon three sections from the Mont Terri area. The macropaleontological, micropaleontological, and palynostratigraphical data are complementary, not only spatially but they also cover almost all biozones from the Late Toarcian to the Early Bajocian. We ran a suite of geophysical logs to determine formational and intraformational boundaries based on clay content in the BDB-1 well. In the framework of an interdisciplinary study, analysis of the above-mentioned formations permitted us to process and derive new and substantial data for the Mont Terri area in a straightforward way. Some parts of the lithologic inventory, stratigraphic architecture, thickness variations, and biostratigraphic classification of the studied formations deviate considerably from occurrences in northern Switzerland that crop out further to the east. For instance, with the exception of the Sissach Member, no further lithostratigraphic subdivision in members is proposed for the Passwang Formation. Also noteworthy is that the ca. 130 m-thick Opalinus Clay in the BDB-1 core is 20 m thinner than that equivalent section found in the Mont Terri tunnel. The lowermost 38 m of the Opalinus Clay can be attributed chronostratigraphically solely to the Aalensis Zone (Late Toarcian). Deposition of the Opalinus Clay began at the same time farther east in northern Switzerland (Aalensis Subzone, Aalensis Zone), but in the Mont Terri area the sedimentation rate was two or three orders of magnitude higher. (authors)

Litho- and biostratigraphy of the Opalinus Clay and bounding formations in the Mont Terri rock laboratory (Switzerland)

Energy Technology Data Exchange (ETDEWEB)

Hostettler, B. [Naturhistorisches Museum der Burgergemeinde Berne, Berne (Switzerland); Reisdorf, A. G. [Geologisch-Paläontologisches InstitutUniversität Basle, Basle (Switzerland); Jaeggi, D. [Swisstopo, Federal Office of Topography, Wabern (Switzerland); and others

2017-04-15

A 250 m-deep inclined well, the Mont Terri BDB-1, was drilled through the Jurassic Opalinus Clay and its bounding formations at the Mont Terri rock laboratory (NW Switzerland). For the first time, a continuous section from (oldest to youngest) the topmost members of the Staffelegg Formation to the basal layers of the Hauptrogenstein Formation is now available in the Mont Terri area. We extensively studied the drill core for lithostratigraphy and biostratigraphy, drawing upon three sections from the Mont Terri area. The macropaleontological, micropaleontological, and palynostratigraphical data are complementary, not only spatially but they also cover almost all biozones from the Late Toarcian to the Early Bajocian. We ran a suite of geophysical logs to determine formational and intraformational boundaries based on clay content in the BDB-1 well. In the framework of an interdisciplinary study, analysis of the above-mentioned formations permitted us to process and derive new and substantial data for the Mont Terri area in a straightforward way. Some parts of the lithologic inventory, stratigraphic architecture, thickness variations, and biostratigraphic classification of the studied formations deviate considerably from occurrences in northern Switzerland that crop out further to the east. For instance, with the exception of the Sissach Member, no further lithostratigraphic subdivision in members is proposed for the Passwang Formation. Also noteworthy is that the ca. 130 m-thick Opalinus Clay in the BDB-1 core is 20 m thinner than that equivalent section found in the Mont Terri tunnel. The lowermost 38 m of the Opalinus Clay can be attributed chronostratigraphically solely to the Aalensis Zone (Late Toarcian). Deposition of the Opalinus Clay began at the same time farther east in northern Switzerland (Aalensis Subzone, Aalensis Zone), but in the Mont Terri area the sedimentation rate was two or three orders of magnitude higher. (authors)

Effects of clay minerals, hydroxides, and timing of dissolved organic matter addition on the competitive sorption of copper, nickel, and zinc : a column experiment

NARCIS (Netherlands)

Refaey, Y.; Jansen, B.; Parsons, J.R.; de Voogt, P.; Bagnis, S.; Markus, A.; El-Shater, A.-H.; El-Haddad, A.-A.; Kalbitz, K.

2017-01-01

Infiltration of heavy metal (HM) polluted wastewater can seriously compromise soil and groundwater quality. Interactions between mineral soil components (e.g. clay minerals) and dissolved organic matter (DOM) play a crucial role in determining HM mobility in soils. In this study, the influence of

New aluminium-rich alkali slag matrix with clay minerals for immobilizing simulated radioactive Sr and Cs waste

International Nuclear Information System (INIS)

Qian Guangren; Sun, Darren Delai; Tay, Joo Hwa

2001-01-01

A new aluminium-rich alkali-activated slag matrix (M-AAS) with clay absorbents has been developed for immobilization of simulated radioactive Sr or Cs waste by introducing metakaolin, natural zeolite and NaOH-treated attapulgite clay minerals into alkali-activated slag matrix (AAS). The results revealed that the additions of metakaolin and clay absorbents into the cementitious matrixes would greatly enhance the distribution ratio, R d , of selective adsorption whether the matrix was OPC matrix or AAS matrix. The new immobilizing matrix M-AAS not only exhibited the strongest selective adsorption for both Sr and Cs ions, but also was characterized by lower porosity and small pore diameter so that it exhibited the lowest leaching rate. Hydration product analyses also demonstrated that (Na+Al)-substituted C-S-H(I) and self-generated zeolite were major hydration products in the M-AAS matrix, which provided this new immobilizing matrix with better selective adsorption on Sr and Cs and lower leaching rate

Removal of Phenol in Aqueous Solution Using Kaolin Mineral Clay

International Nuclear Information System (INIS)

Sayed, M.S.

2008-01-01

Kaolin clay were tested for phenol removal as toxic liquid waste from aqueous waste water. Several experimental conditions such as weight and particle size of clay were investigated to study batch kinetic techniques, also the ph and concentration of the phenol solution were carried out. The stability of the Langmuir adsorption model of the equilibrium data were studied for phenol sorbent clay system. Infrared spectra, thermogravimetric and differential thermal analysis techniques were used to characterize the behavior of kaolin clay and kaolin clay saturated with phenol. The results obtained showed that kaolin clay could be used successfully as an efficient sorbent material to remove phenol from aqueous solution

The growth of multi-walled carbon nanotubes on natural clay minerals (kaolinite, nontronite and sepiolite)

International Nuclear Information System (INIS)

Pastorková, K.; Jesenák, K.; Kadlečíková, M.; Breza, J.; Kolmačka, M.; Čaplovičová, M.; Lazišťan, F.; Michalka, M.

2012-01-01

The suitability of clay minerals - kaolinite, nontronite and sepiolite - is studied for synthesis of nanocomposites based on carbon nanotubes. Particles of iron were used as catalysts. Prior to synthesis, kaolinite and sepiolite were doped by the catalytically active metal, whereas in the case of nontronite the presence was used of this metal in the matrix of this mineral. Synthesis of CNTs was performed by hot filament chemical vapor deposition method. The produced nanocomposites were examined by transmission and scanning electron microscopies and energy dispersive X-ray spectroscopy. The experiment verified the potential of the three microcrystalline phyllosilicates for the growth of carbon nanotubes. Under the same technology conditions, the type of catalyst carrier affects the morphology and structure of the nanotube product markedly.

Multi-technical approach to characterize the dissolved organic matter from clay-stone

International Nuclear Information System (INIS)

Blanchart, Pascale; Michels, Raymond; Faure, Pierre; Parant, Stephane; Bruggeman, Christophe; De Craen, Mieke

2012-01-01

Document available in extended abstract form only. Currently, different clay formations (Boom Clay, Callovo-Oxfordian argilites, Opalinus Clay, Toarcian shales...) are studied as reference host rocks for methodological studies on the geological disposal of high-level and long-lived radioactive waste. While a significant effort is being done on the characterization of the mineral composition and the reactivity of the clays as barriers, the occurrence of organic matter, even in low proportion cannot be neglected. The organic matter appears as gas (C 1 -C 4 as identified in the Bure underground facilities), as solid (kerogen), as hydrocarbon liquids (free hydrocarbons within the kerogen or adsorbed on minerals) as well as in the aqueous phase (Dissolved Organic Matter - DOM). DOM raises specific interest, as it may have complexation properties towards metals and rare earth elements and is potentially mobile. Therefore, it is important to characterize the DOM as part of a study of feasibility of geological disposal. In this study, four host rocks were studied: - The Callovo-Oxfordian shales of Bure Underground Research Laboratory (Meuse, France); - The Opalinus Clay of Mont Terri Underground Research Laboratory (Switzerland); - The Toarcian shales of Tournemire (Aveyron, France); - The Boom Clay formation studied in The HADES Underground Research Laboratory (Mol, Belgium). Organic matter characteristics vary upon formation in terms of (i) origin (mainly marine type II; mixtures of marine type II and higher plants type III organic matter often poorly preserved), (ii) TOC contents, (iii) thermal maturity (for instance, Opalinus Clay and Toarcian shales are more mature and have poor oxygen content compare to Callovo-Oxfordian shales and Boom Clay). These differences in organic matter quality may have an influence on the quantity and the quality of DOM. The DOM of the rocks was isolated by Soxhlet extraction using pure water. A quantitative and qualitative multi

An update on synthetic dyes adsorption onto clay based minerals: A state-of-art review

CSIR Research Space (South Africa)

Ngulube, T

2017-04-01

Full Text Available of Environmental Management An update on synthetic dyes adsorption onto clay based minerals: A state- of-art review Tholiso Ngulube a,*, Jabulani Ray Gumbo b, Vhahangwele Masindi c,d, Arjun Maity e a Department of Ecology and Resources Management..., University of Venda, Private Bag X5050, Thohoyandou, 0950, Limpopo, South Africa b Department of Hydrology and Water Resources, School of Environmental Sciences, University of Venda, Private Bag X5050, Thohoyandou, 0950, Limpopo, South Africa c Council...

Application of solution-mineral equilibrium chemistry to solution mining of uranium ores

International Nuclear Information System (INIS)

Riese, A.C.; Propp, C.J.

1980-01-01

Modern methods of uranium solution mining are typically accompanied by gains and losses of mass through reagent consumption by rock-forming minerals, with subsequent formation of clay minerals, gypsum, carbonates, and iron oxyhydroxides. A systematic approach to alleviate such problems involves the application of leach solutions that are in equilibrium with the host-rock minerals but in disequilibrium with the ore-forming minerals. This partial equilibrium can be approximated by solution-composition adjustments within the systems K 2 O-Al 2 O 3 SiO 2 -H 2 O and Na 2 O 3 -Al 2 O 3 SiO 2 -H 2 O. Uranium ore containing 0.15 percent U 3 O 8 from the Gulf Mineral Resources Corporation's Mariano Lake mine, the Smith Lake district of the Grants mineral belt, was collected for investigation. Presented are a theoretical evaluation of leachate data and an experimental treatment of the ore, which contained mainly K-feldspar, plagioclase feldspar, and quartz (with lesser amounts of micas, clay minerals, and organic carbonaceous material). Small-scale (less than or equal to 1 kg) column-leaching experiments were conducted to model the results of conventional leaching operations and to provide leachate solutions that could be compared with solutions calculated to be in equilibrium with the matrix minerals. Leach solutions employed include: 1) sulfuric acid, 2) sodium bicarbonate, and 3) sulfuric acid with 1.0 molal potassium chloride. The uranium concentrations in the sodium-bicarbonate leach solution and the acid-leach solution were about a gram per liter at the termination of the tests. However, the permeability of the ore in the acid leach was greatly reduced, owing to the formation of clay minerals. Uranium solubility in the leach column stabilized with the potassium-chloride solution was calculated from leachate compositions to be limited by the solubility of carnotite

Geotechnical properties of Karwar marine clay

Digital Repository Service at National Institute of Oceanography (India)

Bhat, S.T.; Nayak, B.U.; Naik, R.L.

Karwar marine clay possesses high plasticity characteristics with natural water content higher than the liquid limit. Liquidity index was as high as 1.7. Predominant clay mineral was kaolinite. Undrained shear strength showed an increasing trend...

Geochemical simulation of the evolution of granitic rocks and clay minerals submitted to a temperature increase in the vicinity of a repository for spent nuclear fuel

International Nuclear Information System (INIS)

Fritz, B.; Kam, M.; Tardy, Y.

1984-07-01

The alteration of a granitic rock around a repository for spent nuclear fuel has been simulated considering the effect of an increase of temperature due to this kind of induced geothermal system. The results of the simulation have been interpreted in terms of mass transfer and volumic consequences. The alteration proceeds by dissolution of minerals (with an increase of the volumes of fissures and cracks) and precipitation of secondary miminerals as calcite and clay minerals particularly (with a decrease of the porosity). The increase of the temperature from 10 degrees C to about 100 degrees C will favour the alteration of the granitic rock around the repository by the solution filling the porosity. The rock is characterized by a very low fissure porosity and a consequent very low water velocity. This too, favours intense water rock interactions and production of secondary clays and the total possible mass transfer will decrease the porosity. A combination of these thermodynamic mass balance calculations with a kinetic approach of mineral dissolutions gives a first attempt to calibrate the modelling in the time scale: the decrease of porosity can be roughly estimated between 2 and 20% for 100,000 years. The particular problem of Na-bentonites behaviour in the proximate vicinity of the repository has been studied too. One must distinguish between two types of clay-water interactions: -within the rock around the repository, Na-bentonites should evolute with illitization in slighltly open system with low clay/water ratios, -within the repository itself, the clay reacts in a closed system for a long time with high clay/water ratios and a self-buffering effect should maintain the bentonite type. This chemical buffering effect is a positive point for the use of this clay as chemical barrier. (Author)

A granulometry and secondary mineral fingerprint of chemical weathering in periglacial landscapes and its application to blockfield origins

Science.gov (United States)

Goodfellow, Bradley W.

2012-12-01

A review of published literature was undertaken to determine if there was a fingerprint of chemical weathering in regoliths subjected to periglacial conditions during their formation. If present, this fingerprint would be applied to the question of when blockfields in periglacial landscapes were initiated. These blocky diamicts are usually considered to represent remnants of regoliths that were chemically weathered under a warm, Neogene climate and therefore indicate surfaces that have undergone only a few metres to a few 10s of metres of erosion during the Quaternary. Based on a comparison of clay and silt abundances and secondary mineral assemblages from blockfields, other regoliths in periglacial settings, and regoliths from non-periglacial settings, a fingerprint of chemical weathering in periglacial landscapes was identified. A mobile regolith origin under, at least seasonal, periglacial conditions is indicated where clay(%) ≤ 0.5*silt(%) + 8 across a sample batch. This contrasts with a mobile regolith origin under non-periglacial conditions, which is indicated where clay(%) ≥ 0.5*silt(%) - 6 across a sample batch with clay(%) ≥ 0.5*silt(%) + 8 in at least one sample. A range of secondary minerals, which frequently includes interstratified minerals and indicates high local variability in leaching conditions, is also commonly present in regoliths exposed to periglacial conditions during their formation. Clay/silt ratios display a threshold response to temperature, related to the freezing point of water, but there is little response to precipitation or regolith residence time. Lithology controls clay and silt abundances, which increase from felsic, through intermediate, to mafic compositions, but does not control clay/silt ratios. Use of a sedigraph or Coulter Counter to determine regolith granulometry systematically indicates lower clay abundances and intra-site variability than use of a pipette or hydrometer. In contrast to clay/silt ratios, secondary

Evolution of multi-mineral formation evaluation using LWD data in complex carbonates offshore Brazil

Energy Technology Data Exchange (ETDEWEB)

Ferraris, Paolo; Borovskaya, Irina [Schlumberger, Houston, TX (United States)

2012-07-01

Petrophysical Formation Evaluation using Logging While Drilling (LWD) measurements is a new requisite when drilling in carbonates reservoirs offshore Brazil. These reservoirs are difficult to characterize due to an unusual mixture of the minerals constituting the matrix and affecting rock texture. As wells are getting deeper and more expensive, an early identification of the drilled targets potential is necessary for valuable decisions. Brazil operators have been especially demanding towards service providers, pushing for development of suitable services able to positively identify and quantify not only the presence of hydrocarbons but also their flowing capability. In addition to the standard gamma ray / resistivity / porosity and density measurements, three new measurements have proven to be critical to evaluate complex carbonate formations: Nuclear Magnetic Resonance (NMR), Spectroscopy and Capture Cross-Section (sigma). Under appropriate logging conditions, NMR data provides lithology independent porosity, bound and free fluids fractions, reservoir texture and permeability. Capture Spectroscopy allows assessment of mineral composition in terms of calcite, dolomite, quartz and clay fractions, and in addition highlights presence of other heavier minerals. Finally, sigma allows performing a volumetric formation evaluation without requiring custom optimization of the classical exponents used in all forms of resistivity saturation equations. All these new measurements are inherently statistical and if provided by wireline after drilling the well they may result in significant usage of rig time. When acquired simultaneously while drilling they have three very clear advantages: 1) no extra rig time, 2) improved statistics due to long formation exposure (drilling these carbonates is a slow process and rate of penetration (ROP) rarely exceeds 10 m/hr), 3) less invasion effect and better hole condition. This paper describes the development of two LWD tools performing the

Sorption of Metal Ions on Clay Minerals.

Science.gov (United States)

Schlegel; Manceau; Chateigner; Charlet

1999-07-01

The local structural environment of Co sorbed on hectorite (a magnesian smectite) has been investigated by polarized EXAFS (P-EXAFS) spectroscopy on a self-supporting film of Co-sorbed hectorite. This sorption sample was prepared by contacting Co and hectorite at pH 6.5 and at high ionic strength (0.3 M NaNO3) to favor pH-dependent sorption reaction over cation exchange. A self-supporting film was elaborated after 120 h of reacting time, when apparent quasi-equilibrium conditions were attained. The half-width at half maximum of the orientation distribution of c* axis of individual clay platelets off the film normal was determined by quantitative texture analysis, and found to be equal to 18.9 degrees. Co K-edge P-EXAFS spectra were recorded at angles between the incident beam and the film normal equal to 0 degrees, 35 degrees, 50 degrees, and 60 degrees; the 90 degrees spectrum was obtained by extrapolation. Spectral analysis led to the identification of the two nearest cationic subshells containing 1.6 +/- 0.4 Mg at 3.03 Å and 2.2 +/- 0.5 Si at 3.27 Å. These distances are respectively characteristic of edge-sharing linkages between Mg and Co octahedra and of corner-sharing linkages between Co octahedra and Si tetrahedra, as in clay structures. The angular dependence of the Co-Mg and Co-Si contributions indicates that Co-Mg pairs are oriented parallel to the film plane, whereas Co-Si pairs are not. These results are interpreted by the formation of Co inner-sphere mononuclear surface complexes located at the edges of hectorite platelets, in the continuity of the (Mg, Li) octahedral sheet. Copyright 1999 Academic Press.

On the role of clay minerals in the disposal of radioactive waste in a clay geological formation; Les mineraux argileux. Leur role et importance dans un site de stockage de dechets radioactifs en couche argileuse profonde

Energy Technology Data Exchange (ETDEWEB)

Clauer, N. [Centre National de la Recherche Scientifique (CNRS), Centre de Geochimie de la Surface, 67 - Strasbourg (France)

2005-05-01

Clay minerals represent appropriate candidates in the search of geological sites and man-made barriers for potential underground storage of nuclear waste, because of their cation-exchange capabilities and swelling properties. However, this statement needs also to take into consideration other aspects such as physical parameters specific (imbrication of the mineral aggregates, occurrence of oxy-hydroxides and/or organic matter), or not of the rocks (temperature, compaction, etc), and the evolutionary history of the target units as they might indirectly modify the above potentials. Alternatively, original micro-discontinuities (micro-fractures) or those induced by the construction of the site do not appear to represent potential drains for fluid escapes, at least over long distances. The few examples presented here emphasize also that one should be careful about generalizing any conclusion, and that analytical data acquisition should be privileged in order to control better the reliability of the results and the potentials of the applied method. (author)

Effects of heat-flow and hydrothermal fluids from volcanic intrusions on authigenic mineralization in sandstone formations

Directory of Open Access Journals (Sweden)

Wolela Ahmed

2002-06-01

Full Text Available Volcanic intrusions and hydrothermal activity have modified the diagenetic minerals. In the Ulster Basin, UK, most of the authigenic mineralization in the Permo-Triassic sandstones pre-dated tertiary volcanic intrusions. The hydrothermal fluids and heat-flow from the volcanic intrusions did not affect quartz and feldspar overgrowths. However, clay mineral-transformation, illite-smectite to illite and chlorite was documented near the volcanic intrusions. Abundant actinolite, illite, chlorite, albite and laumontite cementation of the sand grains were also documented near the volcanic intrusions. The abundance of these cementing minerals decreases away from the volcanic intrusions.In the Hartford Basin, USA, the emplacement of the volcanic intrusions took place simultaneous with sedimentation. The heat-flow from the volcanic intrusions and hydrothermal activity related to the volcanics modified the texture of authigenic minerals. Microcrystalline mosaic albite and quartz developed rather than overgrowths and crystals near the intrusions. Chlorite clumps and masses were also documented with microcrystalline mosaic albite and quartz. These features are localized near the basaltic intrusions. Laumontite is also documented near the volcanic intrusions. The reservoir characteristics of the studied sandstone formations are highly affected by the volcanic and hydrothermal fluids in the Hartford and the Ulster Basin. The porosity dropped from 27.4 to zero percent and permeability from 1350 mD to 1 mD.

Utilization of Nkpuma-Akpatakpa clay in ceramics: characterization ...

African Journals Online (AJOL)

Nkpuma – Akpatakpa clay was analysed for its ceramics suitability. Chemical, mechanical and spectral characterization of the clay was carried out to obtain more information from this clay found in commercial quantity at Ebonyi State Nigeria. The XRD analysis showed that the principal minerals in the clay are quartz, ...

Dynamics of water confined in clay minerals

International Nuclear Information System (INIS)

Le Caer, S.; Pommeret, S.; Renault, J.Ph.; Lima, M.; Righini, R.; Gosset, D.; Simeone, D.; Bergaya, F.

2012-01-01

Ultrafast infrared spectroscopy of the O-D stretching mode of dilute HOD in H 2 O probes the local environment and the hydrogen bond network of confined water. The dynamics of water molecules confined in the interlayer space of montmorillonites (Mt) and in interaction with two types of cations (Li + and Ca 2+ ) but also with the negatively charged siloxane surface are studied. The results evidence that the OD vibrational dynamics is significantly slowed down in confined media: it goes from 1.7 ps in neat water to 2.6 Ps in the case of Li + cations with two water pseudo-layers (2.2-2.3 ps in the case of Ca 2+ cations) and to 4.7 ps in the case of Li + cations with one water pseudo-layer. No significant difference between the two cations is noticed. In this 2D confined geometry (the interlayer space being about 0.6 nm for two water pseudo-layers), the relaxation time constants obtained are comparable to the ones measured in analogous concentrated salt solutions. Nevertheless, and in strong opposition to the observations performed in the liquid phase, anisotropy experiments evidence the absence of rotational motions on a 5 ps time scale, proving that the hydrogen bond network in the interlayer space of the clay mineral is locked at this time scale. (authors)

R and D programme on radioactive waste disposal into a clay formation

International Nuclear Information System (INIS)

Heremans, R.

1984-01-01

The present report presents the main results obtained during the period 1980-82 in the Belgian R and D work on geological disposal of conditioned radioactive waste in the boom clay beneath the Mol site. Multiple research projects have been continued: both experimental research in the field and in the laboratory and theoretical studies. A regional hydrological observation network has been set up which permitted an assessment of the hydrogeological system over- and underlying the Boom clay as well as the modelling of groundwater flow in the area. Clay samples collected during the drilling campaigns were submitted to a number of analyses with a view to chemical characterization and determination of geotechnical properties. Various studies were performed concerning the migration of radionuclides through the clay and an analytical computer model was developed. The corrosion behaviour of various candidate materials for HLW containers and repository linings were tested under different conditions possibly encountered in the clay formation. Furthermore, various backfill and sealing materials and mixtures have been selected and are being tested. Finally, the activities deployed for the safety analysis were continued, mainly concentrated upon two approaches: the probabilistic risk assessment and the performance assessment of a mined repository under normal evolution conditions

Clay fraction mineralogy of a Cambisol in Brazil

Energy Technology Data Exchange (ETDEWEB)

Anastacio, A. S.; Fabris, J. D., E-mail: jdfabris@ufmg.br [Federal University of Minas Gerais, Campus - Pampulha, Department of Chemistry (Brazil); Stucki, J. W. [Department of Natural Resources and Environmental Sciences (United States); Coelho, F. S.; Pinto, I. V. [Federal University of Minas Gerais, Campus - Pampulha, Department of Chemistry (Brazil); Viana, J. H. M. [Embrapa Milho e Sorgo (Brazil)

2005-11-15

Clay minerals having a 2:1 (tetrahedral:octahedral sheet) structure may be found in strongly weathering soils only if the local pedo-climatic environment prevents them from further weathering to other minerals such as iron oxides. The clay minerals impart important chemical properties to soils, in part by virtue of changes in the redox state of iron in their crystal structures. Knowing the chemical nature of soil clays is a first step in evaluating their potential reactivity with other soil constituents and processes, such as the chemical decomposition of organic substrates to be potentially used in environmental remediation. The purpose of this work was to characterize the iron oxides and iron-bearing clay minerals from a B horizon of a Cambisol developed on tuffite in the State of Minas Gerais, Brazil, using chemical analysis, powder X-ray diffraction, Moessbauer spectroscopy, and thermal analysis. The iron oxides of this NaOH-treated clay-fraction were found to contain mainly maghemite ({gamma}Fe{sub 2}O{sub 3}) and superparamagnetic goethite ({alpha}FeOOH). Kaolinite (Al{sub 2}Si{sub 2}O{sub 5}(OH){sub 4}), smectite, and minor portions of anatase (TiO{sub 2}) were identified in the CBD-treated sample.

Evaluation of used fuel disposition in clay-bearing rock

Energy Technology Data Exchange (ETDEWEB)

Jove-Colon, Carlos F. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Hammond, Glenn Edward [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Kuhlman, Kristopher L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Zheng, Liange [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Kim, Kunhwi [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Xu, Hao. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Rutqvist, Jonny [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Caporuscio, Florie Andre [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Norskog, Katherine E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Maner, James [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Palaich, Sarah [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Cheshire, Michael [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Wolery, Thomas J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Atkins-Duffin, Cindy [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Jerden, James L. [Argonne National Lab. (ANL), Argonne, IL (United States); Copple, Jacqueline M. [Argonne National Lab. (ANL), Argonne, IL (United States); Cruse, Terry [Argonne National Lab. (ANL), Argonne, IL (United States); Ebert, William L. [Argonne National Lab. (ANL), Argonne, IL (United States)

2016-09-01

The R&D program from the DOE Used Fuel Disposition Campaign (UFDC) has documented key advances in coupled Thermal-Hydrological-Mechanical-Chemical (THMC) modeling of clay to simulate its complex dynamic behavior in response to thermal and hydrochemical feedbacks. These efforts have been harnessed to assess the isolation performance of heat-generating nuclear waste in a deep geological repository in clay/shale/argillaceous rock formations. This report describes the ongoing disposal R&D efforts on the advancement and refinement of coupled THMC process models, hydrothermal experiments on barrier clay interactions, used fuel and canister material degradation, thermodynamic database development, and reactive transport modeling of the near-field under non-isothermal conditions. These play an important role to the evaluation of sacrificial zones as part of the EBS exposure to thermally-driven chemical and transport processes. Thermal inducement of chemical interactions at EBS domains enhances mineral dissolution/precipitation but also generates mineralogical changes that result in mineral H2O uptake/removal (hydration/dehydration reactions). These processes can result in volume changes that can affect the interface / bulk phase porosities and the mechanical (stress) state of the bentonite barrier. Characterization studies on bentonite barrier samples from the FEBEX-DP international activity have provided important insight on clay barrier microstructures (e.g., microcracks) and interactions at EBS interfaces. Enhancements to the used fuel degradation model outlines the need to include the effects of canister corrosion due the strong influence of H2 generation on the source term.

Transport of vanadium (V in saturated porous media: effects of pH, ionic-strength and clay mineral

Directory of Open Access Journals (Sweden)

Yulu Wang

2016-10-01

Full Text Available Vanadium, a hazardous pollutant, has been frequently detected in soil and groundwater, however, its transport behavior in porous media were not clearly understood. In this study, the effects of solution pH, ionic strength (IS and the effect of clay mineral on the transport of vanadium in saturated porous media were investigated. Laboratory experiments using a series of columns packed with quartz sand were carried out to explore the retention and transport of vanadium with a range of ionic-strength (0.001–0.1 M and pH (4–8 and two different types of clay minerals montmorillonite and kaolinite. Results of the breakthrough experiments showed that vanadium was highly mobile in the saturated porous media. The increase in pH rendered a higher transport of vanadium in saturated porous media. The study also indicated an easier transfer of vanadium with an increase in IS. Montmorillonite enhanced the mobility of vanadium in the column when compared to kaolinite. A mathematical model based on advection-dispersion equation coupled with equilibrium and kinetic reactions was used to describe the retention and transport of vanadium in the columns very well.

Biogeochemical processes in a clay formation in situ experiment: Part A - Overview, experimental design and water data of an experiment in the Opalinus Clay at the Mont Terri Underground Research Laboratory, Switzerland

Energy Technology Data Exchange (ETDEWEB)

Wersin, P., E-mail: paul.wersin@gruner.ch [NAGRA, Hardstrasse 73, 5430 Wettingen (Switzerland)] [Gruner Ltd., Gellertstrasse 55, 4020 Basel (Switzerland); Leupin, O.X. [NAGRA, Hardstrasse 73, 5430 Wettingen (Switzerland); Mettler, S. [NAGRA, Hardstrasse 73, 5430 Wettingen (Switzerland)] [Solexperts Ltd., Mettlenbachstrasse 25, 8617 Moenchaltorf (Switzerland); Gaucher, E.C. [BRGM, 3 avenue Claude Guillemin, B.P. 36009, 45060 Orleans Cedex 2 (France); Maeder, U. [University of Bern, Institute of Geological Sciences, Baltzerstrasse 3, CH-3012 Bern (Switzerland); De Canniere, P. [SCK.CEN, Waste and Disposal Project, Boeretang 200, 2400 Mol (Belgium); Vinsot, A. [ANDRA, Laboratoire de Recherche Souterrain de Meuse/Haute-Marne, RD960 BP9, 55290 Bure (France); Gaebler, H.E. [BGR, Stilleweg 2, 30655 Hannover (Germany); Kunimaro, T. [JAEA, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Kiho, K. [CRIEPI, 1646 Abiko, Abiko-city Chiba 270-1194 (Japan); Eichinger, L. [Hydroisotop, 85301 Schweitenkirchen (Germany)

2011-06-15

Highlights: > The composition was affected by the complex interplay of diffusion, mineral and surface reactions. > The {sup 13}C signals for carbon species showed significant variations which could only be partly explained. > The main cations remained remarkably constant during the experiment. > This underlines the strong buffering via cation exchange and carbonate dissolution/precipitation. - Abstract: An in situ test in the Opalinus Clay formation, termed porewater chemistry (PC) experiment, was carried out for a period of 5 years. It was based on the concept of diffusive equilibration whereby a traced water with a composition close to that expected in the formation was continuously circulated and monitored in a packed-off borehole. The main original focus was to obtain reliable data on the pH/pCO{sub 2} conditions of the porewater, but because of unexpected microbiologically-induced redox reactions, the objective was extended to elucidate the biogeochemical processes occurring in the borehole and to understand their impact on pH/pCO{sub 2} and porewater chemistry in the low permeability clay formation. The behaviour of the conservative tracers {sup 2}H and Br{sup -} could be explained by diffusive dilution in the clay and moreover the results showed that diffusive equilibration between the borehole water and the formation occurred within about 3 year's time. However, the composition and pH/pCO{sub 2} conditions differed considerably from those of the in situ porewater. Thus, pH was lower and pCO{sub 2} was higher than indicated by complementary laboratory investigations. The noted differences are explained by microbiologically-induced redox reactions occurring in the borehole and in the interfacial wall area which were caused by an organic source released from the equipment material. The degradation of this source was accompanied by sulfate reduction and - to a lesser extent - by methane generation, which induced a high rate of acetogenic reactions

Impact of Oriented Clay Particles on X-Ray Spectroscopy Analysis

Science.gov (United States)

Lim, A. J. M. S.; Syazwani, R. N.; Wijeyesekera, D. C.

2016-07-01

Understanding the engineering properties of the mineralogy and microfabic of clayey soils is very complex and thus very difficult for soil characterization. Micromechanics of soils recognize that the micro structure and mineralogy of clay have a significant influence on its engineering behaviour. To achieve a more reliable quantitative evaluation of clay mineralogy, a proper sample preparation technique for quantitative clay mineral analysis is necessary. This paper presents the quantitative evaluation of elemental analysis and chemical characterization of oriented and random oriented clay particles using X-ray spectroscopy. Three different types of clays namely marine clay, bentonite and kaolin clay were studied. The oriented samples were prepared by placing the dispersed clay in water and left to settle on porous ceramic tiles by applying a relatively weak suction through a vacuum pump. Images form a Scanning Electron Microscope (SEM) was also used to show the comparison between the orientation patterns of both the sample preparation techniques. From the quantitative analysis of the X-ray spectroscopy, oriented sampling method showed more accuracy in identifying mineral deposits, because it produced better peak intensity on the spectrum and more mineral content can be identified compared to randomly oriented samples.

The importance of mobile fission products for long-term safety in the case of disposal of vitrified high-level waste and spent fuel in a clay formation

International Nuclear Information System (INIS)

Marivoet, J.; Weetjens, E.

2009-01-01

In Belgium, the possibility to dispose of high-level radioactive waste in clay formations is studied since 1976. In the PAGIS report, which was the first performance assessment of the disposal of vitrified high-level waste in a clay formation and which was published in 1988, the most important contributors to the total dose via a water well pathway were 237 Np, 135 Cs and 99 Tc. Since 1988, several elements that strongly influence the calculated doses have evolved:?the inventory of long-lived mobile fission and activation products in vitrified high-level waste has been improved; the half-life of 79 Se has been re-estimated; substantial progress has been made in the determination of migration parameters of the main fission and activation products and actinides. In recent performance assessments, the actinides and 135 Cs do not significantly contribute to the total dose, as they remain confined in the host clay formation during several millions of years due to sorption on clay minerals. Consequently, the total dose resulting from the disposal of vitrified high-level waste or spent fuel is essentially due to releases of mobile fission and activation products. On the basis of recent waste inventory data and parameter values, the most important contributors to the total dose via a water well are: in the case of disposal of spent fuel: 79 Se, 129 I, 126 Sn, 36 Cl, and 99 Tc; in the case of disposal of vitrified HLW: 79 Se, 126 Sn, 36 Cl, 129 I, and 99 Tc. Important remaining uncertainties are the transfer factors of volatile fission and activation products into the vitrified waste during reprocessing and migration parameters of Se. (author)

Investigation of Phosphate Retention in some Allophanic and Non-Allophanic Nano-Clays from Karaj Formation

Directory of Open Access Journals (Sweden)

Mohammad Ali Monajjem

2017-02-01

Full Text Available Introduction: Nanoclays, due to their high specific surface area (SSA chemical and mechanical stabilities, and a variety of surface and structural properties are widely applied. Some of their applications are using them as nano composite polymers, heavy metal ions absorbents, catalysts, photochemical reaction fields, ceramics, paper fillings and coatings, sensors and biosensors. Nano clays and Clays are the most important components constructing soil ecosystems. The physical and chemical properties of soils are mainly depending on the type and amount their clay fraction pertaining to considerable nanoclays. Nano clays have been frequently used to eliminate environmental contaminants from soil and water. Nano clays have also an effective role in the phosphate sorption and desorption from soil solution. Phosphate retention is highly affected by the chemical bonds of the materials, cristalographic properties and pH. In clay size particles there are different structures of nano particles such as alominosilicates with nano ball and nano tube construction. Soils with andic properties have amorphous clay minerals such as allophone. Allophane has a diameter of 3 to 5 nano meter under a transmission electron microscope (TEM and its atomic Si/Al ratio ranges between 0.5 and 1. Allophane shows variable charge characteristics and high selectivity for divalent cations, and is highly reactive with phosphate. Materials and Methods: The objective of this research was to inspect the effect of soil components particularly clay and nanoclay on the sorption of phosphate. To achieve this goal, we studied the amount of phosphate sorption by the natural nanoclays. Samples with andic and vitric properties which were previously formed on volcanic ash in Karaj were chosen in 5 pedons as two Andic ( > 5 percent volcanic glass, > 25 percent P retention, pH NaF > 8.6 and Alo +½ Feo > 0.4 and non Andic soils.. After removal of organic materials, soluble salts, carbonates

Continental weathering as a driver of Late Cretaceous cooling: new insights from clay mineralogy of Campanian sediments from the southern Tethyan margin to the Boreal realm

Science.gov (United States)

Chenot, Elise; Deconinck, Jean-François; Pucéat, Emmanuelle; Pellenard, Pierre; Guiraud, Michel; Jaubert, Maxime; Jarvis, Ian; Thibault, Nicolas; Cocquerez, Théophile; Bruneau, Ludovic; Razmjooei, Mohammad J.; Boussaha, Myriam; Richard, James; Sizun, Jean-Pierre; Stemmerik, Lars

2018-03-01

New clay mineralogical analyses have been performed on Campanian sediments from the Tethyan and Boreal realms along a palaeolatitudinal transect from 45° to 20°N (Danish Basin, North Sea, Paris Basin, Mons Basin, Aquitaine Basin, Umbria-Marche Basin and Tunisian Atlas). Significant terrigenous inputs are evidenced by increasing proportions of detrital clay minerals such as illite, kaolinite and chlorite at various levels in the mid- to upper Campanian, while smectitic minerals predominate and represented the background of the Late Cretaceous clay sedimentation. Our new results highlight a distinct latitudinal distribution of clay minerals, with the occurrence of kaolinite in southern sections and an almost total absence of this mineral in northern areas. This latitudinal trend points to an at least partial climatic control on clay mineral sedimentation, with a humid zone developed between 20° and 35°N. The association and co-evolution of illite, chlorite and kaolinite in most sections suggest a reworking of these minerals from basement rocks weathered by hydrolysis, which we link to the formation of relief around the Tethys due to compression associated with incipient Tethyan closure. Diachronism in the occurrence of detrital minerals between sections, with detrital input starting earlier during the Santonian in the south than in the north, highlights the northward progression of the deformation related to the anticlockwise rotation of Africa. Increasing continental weathering and erosion, evidenced by our clay mineralogical data through the Campanian, may have resulted in enhanced CO2 consumption by silicate weathering, thereby contributing to Late Cretaceous climatic cooling.

Nanoporous polymer--clay hybrid membranes for gas separation.

Science.gov (United States)

Defontaine, Guillaume; Barichard, Anne; Letaief, Sadok; Feng, Chaoyang; Matsuura, Takeshi; Detellier, Christian

2010-03-15

Nanohybrid organo-inorgano clay mineral-polydimethylsiloxane (PDMS) membranes were prepared by the reaction of pure and/or modified natural clay minerals (Sepiolite and montmorillonite) with PDMS in hexane, followed by evaporation of the solvent at 70 degrees C. The membranes were characterized by means of XRD, SEM, ATD-TG and solid state (29)Si magic angle spinning (MAS) and cross-polarization (CP) CP/MAS NMR. The morphology of the membranes depends on the content loading of clay mineral. For low content, the membrane composition is homogeneous, with well dispersed nanoparticles of clay into the polymer matrix, whereas for higher clay content, the membranes are constituted also of a mixture of well dispersed nanoparticles into the polymer, but in the presence of agglomerations of small clay particles. Quantitative (29)Si MAS NMR demonstrated a strong correlation between the clay content of the membrane and the average length of the PDMS chain, indicating that the nanohybrid material is made of clay particles covalently linked to the PDMS structure. This is particularly the case for Sepiolite with has a high density of Q(2) silanol sites. The separation performances of the prepared membranes were tested for CO(2)/CH(4) and O(2)/N(2) mixtures. The observed separation factors showed an increase of the selectivity in the case of CO(2)/CH(4) in comparison with membranes made from PDMS alone under the same conditions. 2009 Elsevier Inc. All rights reserved.

Synthesis and Characterization of the Hybrid Clay- Based Material Montmorillonite-Melanoidin: A Potential Soil Model

Energy Technology Data Exchange (ETDEWEB)

V Vilas; B Matthiasch; J Huth; J Kratz; S Rubert de la Rosa; P Michel; T Schäfer

2011-12-31

The study of the interactions among metals, minerals, and humic substances is essential in understanding the migration of inorganic pollutants in the geosphere. A considerable amount of organic matter in the environment is associated with clay minerals. To understand the role of organic matter in the environment and its association with clay minerals, a hybrid clay-based material (HCM), montmorillonite (STx-1)-melanoidin, was prepared from L-tyrosine and L-glutamic acid by the Maillard reaction. The HCM was characterized by elemental analysis, nuclear magnetic resonance, x-ray photoelectron spectroscopy (XPS), scanning transmission x-ray microscopy (STXM), and thermal analysis. The presence of organic materials on the surface was confirmed by XPS and STXM. The STXM results showed the presence of organic spots on the surface of the STx-1 and the characterization of the functional groups present in those spots. Thermal analysis confirmed the existence of organic materials in the montmorillonite interlayer, indicating the formation of a composite of melanoidin and montmorillonite. The melanoidin appeared to be located partially between the layers of montmorillonite and partially at the surface, forming a structure that resembles the way a cork sits on the top of a champagne bottle.

First principles molecular dynamics insight into acid-base chemistry of clay minerals

International Nuclear Information System (INIS)

Liu, Xiandong; Lu, Xiancai; Wang, Rucheng; Meijer, Evert Jan

2012-01-01

Document available in extended abstract form only. Microscopic knowledge on the interfaces between clay minerals (2:1- and 1:1-type) and water is critical for both understanding natural processes and guiding development of advanced hybrid materials. Due to the unique layered structures of clay minerals, their surfaces are usually grouped into basal surfaces and edge surfaces (i.e. broken surfaces). Thanks to previous studies, structures and properties of basal surfaces have been well recognized: these surfaces are terminated with siloxanes and surface Si-O six-member rings normally act as the adsorbing sites of cations. In contrast, edge surfaces are more complicated structures and have more subtle chemical properties. On these surfaces, there are a lot of dangling bonds and under ambient conditions they are usually saturated by chemically adsorbed waters. These edge groups are usually amphoteric, which is responsible to the pH dependent behaviors of many interfacial processes, such as cations complexing. For example, adsorption of heavy metal cations (e.g. Ni 2+ , Co 2+ , Zn 2+ , Cd 2+ ) on clay basal surfaces is through cation exchange mechanism and that is hardly influenced by environmental pH. In contrast, it has been well accepted that the adsorption on edge surfaces is pH-dependent. The ubiquitous isomorphic substitutions further increase the complexity of their interfacial chemistry. Due to the high heterogeneity and rather small sizes, it is quite difficult to reveal the complex interfacial chemistry with experiments alone. FPMD method (first principles molecular dynamics), a combination of density functional theory and molecular dynamics, can provide valuable information. With FPMD [1, 2] and free-energy calculation techniques [3, 4], we investigated the microscopic structures and acid chemistry of these clay-water interfaces [5, 6]. According to systematic simulations, the following has been achieved. (1) Acidity of interlayer waters. The simulations show

Absorption characteristics of Kupravas deposit clays modified by phosphoric acid

International Nuclear Information System (INIS)

Ruplis, A.; Mezinskis, G.; Chaghuri, M.

1998-01-01

Literature data suggested that clays may be used as sorbents for waste water treatment. The surface and sorption properties of minerals changes due to the influence of acid rains. The process of recession of clay properties has been modeled in laboratory by treatment of clays with mineral acids at higher temperature that in natural conditions. The present paper is devoted to the study of influence of phosphoric acid on the sorption properties of Kupravas deposit clays. Natural clay samples and samples treated with phosphoric acid were characterized by means of x-ray diffraction an differential thermal analysis (DTA) methods These methods were used also to identify the sample of Lebanese clays. X-ray diffraction analysis data show that the samples of clays from the deposit of Kuprava contain illite and kaolinite while sample of Lebanese clay contains quartz, calcite, and montmorillonite. DTA results show characteristic features of Kuprava clays described in reference with DTA of Lebanese clay clearly demonstrate the presence of large quantity of calcite

Studies on thermal reactions and sintering behaviour of red clays by irreversible dilatometry

Science.gov (United States)

Anil, Asha; Misra, S. N.; Misra, N. M.

2018-05-01

Thermal behavior of clays strongly influences that of ceramic bodies made thereof and hence, its study is must for assessing its utility in ceramic products as well as to set the body composition. Irreversible dilatometry is an effective thermal analysis tool for evaluating thermal reactions as well as sintering behavior of clays or clay based ceramic bodies. In this study, irreversible dilatometry of four red clay samples (S, M, R and G) of Gujarat region, which vary in their chemical and mineralogical compositions was carried out using a Dilatometer and compared. Chemical analysis and XRD of red clays were carried out. XRD showed that major clay minerals in S, M and R clays are kaolinite. However, clay marked R and G showed presence of both kaolinite and illite and /muscovite. Presence of non-clay minerals such as hematite, quartz, anatase were also observed in all clays. XRD results were in agreement with chemical analyses results. Rational analyses showed variation in amount of clay and non-clay minerals in red clay samples. Evaluation of dilatometric curves showed that clay marked as S, M and R exhibit patterns typical for kaolinitic clays. Variation in linear expansion (up to 550°C) and shrinkage (above 550°C) between these three clays was found to be related to difference in amount of quartz and kaolinite respectively. However, dilatometric curve of G exhibit a pattern similar to that for an illitic clay. This study confirmed that sintering of investigated kaolinitic and illitic and / muscovitic red clays initiates at above 1060°C and 860°C respectively and this behaviour strongly depends upon type and amount of minerals and their chemical compositions.

Oxygen isotope fractionation effects in soil water via interaction with cations (Mg, Ca, K, Na) adsorbed to phyllosilicate clay minerals

Science.gov (United States)

Oerter, Erik; Finstad, Kari; Schaefer, Justin; Goldsmith, Gregory R.; Dawson, Todd; Amundson, Ronald

2014-07-01

In isotope-enabled hydrology, soil and vadose zone sediments have been generally considered to be isotopically inert with respect to the water they host. This is inconsistent with knowledge that clay particles possessing an electronegative surface charge and resulting cation exchange capacity (CEC) interact with a wide range of solutes which, in the absence of clays, have been shown to exhibit δ18O isotope effects that vary in relation to the ionic strength of the solutions. To investigate the isotope effects caused by high CEC clays in mineral-water systems, we created a series of monominerallic-water mixtures at gravimetric water contents ranging from 5% to 32%, consisting of pure deionized water of known isotopic composition with homoionic (Mg, Ca, Na, K) montmorillonite. Similar mixtures were also created with quartz to determine the isotope effect of non-, or very minimally-, charged mineral surfaces. The δ18O value of the water in these monominerallic soil analogs was then measured by isotope ratio mass spectrometry (IRMS) after direct headspace CO2 equilibration. Mg- and Ca-exchanged homoionic montmorillonite depleted measured δ18O values up to 1.55‰ relative to pure water at 5% water content, declining to 0.49‰ depletion at 30% water content. K-montmorillonite enriched measured δ18O values up to 0.86‰ at 5% water content, declining to 0.11‰ enrichment at 30% water. Na-montmorillonite produces no measureable isotope effect. The isotope effects observed in these experiments may be present in natural, high-clay soils and sediments. These findings have relevance to the interpretation of results of direct CO2-water equilibration approaches to the measurement of the δ18O value of soil water. The adsorbed cation isotope effect may bear consideration in studies of pedogenic carbonate, plant-soil water use and soil-atmosphere interaction. Finally, the observed isotope effects may prove useful as molecular scale probes of the nature of mineral

Possibility of disposing of conditioned nuclear waste in deep-lying clay formations

International Nuclear Information System (INIS)

Bonne, A.; Heremans, R.; Vandenberghe, N.

1980-01-01

Among the host rock types suitable for final disposal of nuclear waste, argillaceous formations display distinct advantages and disadvantages. In the present paper some of them will be examined. In order to render conceivable the possibilities for disposing of radwastes into a plastic clay formation, some main items of the Belgian R and D-programme in that matter will be discussed (site and rock investigation, conceptual design and feasibility, and risk analysis). (Auth.)

Flocculation - Formation and structure of aggregates composed of polyelectrolyte chains and clay colloidal particles

OpenAIRE

Sakhawoth , Yasine

2017-01-01

Flocculation is a key process in numerous environmental and industrial technologies such as purification of waste-water or paper making. It is necessary to understand the formation and structure of the aggregates to control and optimize such a process. Most of the studies on flocculation involve spherical particles, but there is a clear need to understand the flocculation of anisotropic particles such as clay colloids, which are platelets. I studied the flocculation of montmorillonite clay su...

Surface Assisted Formation of methane Hydrates on Ice and Na Montmorillonite Clay

Energy Technology Data Exchange (ETDEWEB)

Gordon, Margaret Ellen [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Teich-McGoldrick, Stephanie [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Cygan, Randall Timothy [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Meserole, Stephen P. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Rodriguez, Mark A. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

2015-07-01

Methane hydrates are extremely important naturally-occurring crystalline materials that impact climate change, energy resources, geological hazards, and other major environmental issues. Whereas significant experimental effort has been completed to understanding the bulk thermodynamics of methane hydrate assemblies, little is understood on heterogeneous nucleation and growth of methane hydrates in clay-rich environments. Controlled synthesis experiments were completed at 265-285 K and 6.89 MPa to examine the impact of montmorillonite surfaces in clay-ice mixtures to nucleate and form methane hydrate. The results suggest that the hydrophilic and methane adsorbing properties of Namontmorillonite reduce the nucleation period of methane hydrate formation in pure ice systems.

Studying the Effect of Crystal Size on Adsorption Properties of Clay

International Nuclear Information System (INIS)

Abdellatif, M.M.

2012-01-01

Sorption of radionuclides on mineral surfaces strongly affects their fate and mobility in the geosphere. Therefore using of clay minerals as a barrier In LLW repositories can delay the dispersion of radionuclides into environment. That is of fundamental importance for maintaining environmental quality and for the safety and long-term performance of waste repositories. In this study XRD analysis was applied to investigate three different types of clay minerals for quantitative analysis of each type and the Mud Master program for the measurement of the crystallite thickness distribution (CTD) according to of the BWA (Bertaut-Warren Averbach) technique. Six sample s of the three types of clay (Kaolin, Aswan clay and Ball clay) were studied. XRD and Mud Master were used to investigate the relation between CTD and Cs -137 uptake mechanism onto the clay. It was found that the best adsorption capacity related to the kaolinite content and the lowest CTD

Clay minerals, metallic oxides and oxy-hydroxides and soil organic carbon distribution within soil aggregates in temperate forest soils

Science.gov (United States)

Gartzia-Bengoetxea, Nahia; Fernández-Ugalde, Oihane; Virto, Iñigo; Arias-González, Ander

2017-04-01

Soil mineralogy is of primary importance for key environmental services provided by soils like carbon sequestration. However, current knowledge on the effects of clay mineralogy on soil organic carbon (SOC) stabilization is based on limited and conflicting data. In this study, we investigated the relationship between clay minerals, metallic oxides and oxy-hydroxides and SOC distribution within soil aggregates in mature Pinus radiata D.Don forest plantations. Nine forest stands located in the same geographical area of the Basque Country (North of Spain) were selected. These stands were planted on different parent material (3 on each of the following: sandstone, basalt and trachyte). There were no significant differences in climate and forest management among them. Moreover, soils under these plantations presented similar content of clay particles. We determined bulk SOC storage, clay mineralogy, the content of Fe-Si-Al-oxides and oxyhydroxides and the distribution of organic C in different soil aggregate sizes at different soil depths (0-5 cm and 5-20 cm). The relationship between SOC and abiotic factors was investigated using a factor analysis (PCA) followed by stepwise regression analysis. Soils developed on sandstone showed significantly lower concentration of SOC (29 g C kg-1) than soils developed on basalts (97 g C kg-1) and trachytes (119 g C kg-1). The soils on sandstone presented a mixed clay mineralogy dominated by illite, with lesser amounts of hydroxivermiculite, hydrobiotite and kaolinite, and a total absence of interstratified chlorite/vermiculite. In contrast, the major crystalline clay mineral identified in the soils developed on volcanic rocks was interstratified chlorite/vermiculite. Nevertheless, no major differences were observed between basaltic and trachytic soils in the clay mineralogy. The selective extraction of Fe showed that the oxalate extractable iron was significantly lower in soils on sandstone (3.7%) than on basalts (11.2%) and

Action of a clay suspension on an Fe(0) surface under anoxic conditions: Characterization of neoformed minerals at the Fe(0)/solution and Fe(0)/atmosphere interfaces

International Nuclear Information System (INIS)

Le Pape, Pierre; Rivard, Camille; Pelletier, Manuel; Bihannic, Isabelle; Gley, Renaud; Mathieu, Sandrine; Salsi, Lise; Migot, Sylvie; Barres, Odile; Villiéras, Frédéric; Michau, Nicolas

2015-01-01

Highlights: • Immersion of an Fe(0) foil in a clay suspension at 90 °C and in anoxic conditions. • Magnetite was observed on the atmospheric part. • Iron-rich 7 Å serpentines were observed on the clay suspension part. • A gradient in serpentine cristallochemistry was observed. • A pure Fe–Si phyllosilicate was identified at the Fe(0)/clay suspension contact. - Abstract: To better understand the reaction mechanisms involved at the Fe(0)/clay minerals interface, we investigate in the present study the reaction between an Fe(0) surface and a clay suspension extracted from the Callovo-Oxfordian claystone (COx). Batch experiments were carried out under anoxic conditions in sealed autoclave, at 90 °C to mimic predicted radioactive waste disposal conditions. An Fe(0) foil was introduced into the autoclave so that the lower part of the foil was immersed in the clay suspension while the upper part was contacted with the atmosphere of the experimental setup. After two months, the mineralogical deposits that precipitated at the surface of the Fe(0) foil were analyzed using multiple techniques, namely X-ray diffraction (XRD), scanning/transmission electron microscopy associated to microanalysis (SEM/TEM–EDXS), and micro-spectroscopic measurements (μ-FTIR and μ-Raman). Both parts of the Fe(0) foil were then shown to react: magnetite was the main resulting mineral formed at the Fe(0) surface in the atmospheric conditions whereas serpentine 1:1 phyllosilicates were the main end-products in the clay suspension. The analyses performed on the immersed part of the foil revealed a spatial heterogeneity in both serpentine cristallochemistry and morphology, with a gradient from the Fe(0) contact point toward the clay suspension. A pure Fe–Si phyllosilicate ring was observed at the direct contact point with the Fe(0) foil and a progressive incorporation of Al instead of Fe into the clay phases was identified as deposit thickness increased from the Fe(0) surface to

Characterization of clay used for red ceramic fabrication

International Nuclear Information System (INIS)

Pereira, P.S.; Morais, A.S.C.; Caldas, T.C.C.; Monteiro, S.N.; Vieira, C.M.F.

2011-01-01

The objective of this work is to characterize a clay used in the red ceramics fabrication, from Campos dos Goytacazes north of the State of Rio de Janeiro. The clay was submitted for physical, chemical and mineralogical tests. The results showed that the clay has a high content of clay minerals with kaolinitic predominance, high loss on ignition and low flux oxides. It is recommended that this clay is mixed with non-plastic materials. (author)

Pulse heating tests on two reference Belgian clay formations. Laboratory experiments and numerical study

International Nuclear Information System (INIS)

Lima, A.; Romero, E.; Vaunat, J.; Gens, A.; Li, X.L.

2012-01-01

Document available in extended abstract form only. Two deep clay formations are being investigated in Belgium in connection with the design of a repository for 'High-Level Radioactive Waste': Boom clay at Mol (located between 160 and 270 m depths), considered the reference host formation, and Ypresian clay at Kallo (located between 300 and 450 m depths) as an alternative one. Thermal impact may play an important role on the behaviour of these low-permeability clayey formations. In this context, heating pulse tests on intact borehole samples retrieved in vertical and horizontal directions were carried out on both clays using an axisymmetric heating cell. Heating tests under nearly constant volume conditions and different target temperatures (maximum 85 C) were performed under controlled hydraulic boundary conditions. Attention is focused on the time evolution of temperature and pore water pressure changes during heating and cooling paths -i.e., pore pressure build-up during quasi-undrained heating and later dissipation to the applied hydraulic boundary conditions-. The finite element program CODE-BRIGHT was used to determine thermal parameters by back-analysis and to simulate the experimental results. Table 1 summarises the main properties of these clays. The experimental programme was carried out on a fully-instrumented cell (sample 75 mm diameter and 100 mm high) with a controlled-power heater housed inside the cell. Two miniature pore water pressure transducers located at different heights of the lateral wall of the cell and three thermocouples were used to monitor the sample response. The cell has top and bottom valves to control hydraulic conditions. The protocol of the tests included three main phases: hydration, heating and cooling. Throughout the heating and cooling phases, the bottom drainage was maintained open at a constant water pressure using an automatic pressure/volume controller, while the upper valve was kept closed. Figures 1a and 1c show the time

A new avian fauna from the early-middle Eocene Lillebælt Clay Formation of Denmark

DEFF Research Database (Denmark)

Lindow, Bent Erik Kramer

A number of hitherto undescribed fossil bird remains have been recovered from the Lillebælt Clay Formation of central Denmark, which is early-middle Eocene in age (~50 to 43 mya). The core of the material consists of fossils acquired through the Danish ‘Danekræ' fossil treasure trove legislation......, a member of the extinct 'pseudo-toothed birds' and the first representative of this group known from Denmark. Other taxa present include remains of Lithornithidae and a new taxon possessing a massive, psittacid-like beak. The Lillebælt Clay Formation birds are temporally placed just after the Early Eocene...

Influence of organic matter and clay minerals in migration of derivative compounds of hydrocarbons; Influencia da materia organica e argilominerais na migracao de compostos derivados de hidrocarbonetos

Energy Technology Data Exchange (ETDEWEB)

Ramos, Denize Gloria Barcellos; Mendonca Filho, Joao Graciano de; Polivanov, Helena [Universidade Federal, Rio de Janeiro, RJ (Brazil). Inst. de Geociencias. Dept. de Geologia]. E-mail: denize@geologia.ufrj.br; graciano@geologia.ufrj.br; helena@acd.ufrj.br

2003-07-01

Soil samples from the Guanabara Bay in Duque de Caxias city (RJ) were submitted to mineralogical and organic geochemistry analyses. This proceeding was used mainly to determine a possible interaction of hydrocarbons contaminants with the organic matter and the clay minerals presents in this mangrove. The sampling was carried out using Direct Push techniques. Thus, the mainly clay minerals characterizes were: gibbsite, illite, caulinite and smectite. The compositional analysis of organic constituents showed a predominance of amorphous material (degraded cuticles), followed of wood material and sporomorphs constituents, suggesting that the biological degradation occurred in situ. (author)

Experience acquired with the realisation of a geotechnical measurement campaign in a deep clay formation

International Nuclear Information System (INIS)

Manfroy, P.; Neerdael, B.; Buyens, M.

1985-01-01

Belgium has selected clay as a possible disposal medium for conditioned radioactive waste. CEN/SCK has launched an important research and development programme to evaluate the disposal potential of the Boom clay formation present under the nuclear site Mol-Dessel. An underground facility has been built at 220 m. depth in order to proceed to geomechanical, corrosion, migration and heat transfer experiments. During its construction numerous geotechnical measuring instruments were emplaced on the lining and in the clay medium. Successful realization of such measurement campaigns was hampered by the very difficult underground working conditions. This paper describes what can be learned from the experience gained so far. 5 refs.; 5 figs

Vesicular delivery of crystalline calcium minerals to ECM in biomineralized nanoclay composites

International Nuclear Information System (INIS)

Katti, Kalpana S; Ambre, Avinash H; Payne, Scott; Katti, Dinesh R

2015-01-01

The mechanisms of mineralization and new bone formation were explored in newly formed extracellular matrix in a nanoclay based composite. Nanoclay films were prepared by intercalating the clays with amino acids and using the amino acids for mineralization of hydroxyapatite. The biomineralized hydroxyapatite (HAP) inside nanoclay galleries or in situ HAP/clay was further used to make films (substrates) using polycaprolactone (PCL) that were seeded with mesenchymal stem cells in a two-stage seeding process. SEM imaging experiments performed on PCL/in situ HAPclay composite films seeded with human MSCs indicated formation of matrix vesicles. The vesicles appear to emerge from the cells that are adhered to the nanoclay HAP films and also deposited in the extracellular space. Vesicles are also observed to be embedded in the cells or under the surface of cells. Crystalline structures with Ca and P were found inside vesicles. The Ca/P ratios obtained using energy dispersive spectroscopy indicate values ranging from below 0.7 to the stoichiometric HAP value of 1.67. The Ca/P ratios were obtained to be closer to the stoichiometric value for single seeding experiments as compared to the double seeding experiments indicating more new bone formation in double seeding experiments. New bone formation with bone mimetic mineralization is thus observed on the in situ HAP nanoclay PCL samples. Hence the PCL/in situ HAPclay composites besides being osteoinductive are also capable of providing a favorable micro-environment for cell dependent processes involved in bone mineral formation. (paper)

Change effects in the land use about the mineral clay

International Nuclear Information System (INIS)

Cespedes Payret, C.; Gutierrez, O; Panario, D.; Pineiro, G

2012-01-01

The Pampas land changes during the Quaternary, left their mark on the mineralogy of soil clays. This work is oriented to compare the mineralogical composition of the clays and the value of potassium in an eucalyptus forestation. These results show that the mineralogical illite alteration is the cause of its destruction. This clay is the main reservoir of potassium for the agricultural soils

Water-clay interactions. Experimental study

International Nuclear Information System (INIS)

Gaucher, Eric

1998-01-01

Clay minerals contribute to the chemical composition of soil and sediment groundwaters via surface and dissolution/precipitation reactions. The understanding of those processes is still today fragmentary. In this context, our experimental purpose is to identify the contribution of each reaction in the chemical composition of water in a water/clay System. Kaolinite, illite, montmorillonite are the reference clays. After a fine mineralogical study, the exchange equilibria between K + and H + are characterised. Different exchange sites are identified and the exchange capacities and selectivity coefficients are quantified. Then, mixtures of the three clays are equilibrated with acidic and basic (I≤10 -2 M) solutions at 25 deg. C, 60 deg. C, 80 deg. C, during 320 days. The System evolution is observed by chemical analysis of the solutions and mineralogical analysis by TEM. We show that montmorillonite is unstable compared to the kaolinite/amorphous silica assemblage for solutions of pH<7. Aqueous silica is probably controlled by the kinetics of dissolution of the montmorillonite in moderate pH media. In more acidic solutions, amorphous silica precipitates. Al is under control of 'kaolinite' neo-formations. The use of the selectivity coefficients in a numerical simulation shows that K + concentration depends on exchange reactions. The pH has a more complicated evolution, which is not completely understood. This evolution depends on both exchange equilibria and organic acid occurrence. In this type of experiments, we have demonstrated that the equilibrium equations between smectite and kaolinite are inexact. The problem of the thermodynamic nature of clays remains and is not resolved by these solubility experiments. (author) [fr

Experimental study and modelling of selenite sorption onto illite and smectite clays.

Science.gov (United States)

Missana, T; Alonso, U; García-Gutiérrez, M

2009-06-15

This study provides a large set of experimental selenite sorption data for pure smectite and illite. Similar sorption behavior existed in both clays: linear within a large range of the Se concentrations investigated (from 1x10(-10) to 1x10(-3) M); and independent of ionic strength. Selenite sorption was also analysed in the illite/smectite system with the clays mixed in two different proportions, as follows: (a) 30% illite-70% smectite and (b) 43% illite-57% smectite. The objective of the study was to provide the simplest model possible to fit the experimental data, a model also capable of describing selenite sorption in binary illite/smectite clay systems. Selenite sorption data, separately obtained in the single mineral systems, were modeled using both a one- and a two-site non-electrostatic model that took into account the formation of two complexes at the edge sites of the clay. Although the use of a two-site model slightly improved the fit of data at a pH below 4, the simpler one-site model reproduced satisfactorily all the sorption data from pH 3 to 8. The complexation constants obtained by fitting sorption data of the individual minerals were incorporated into a model to predict the adsorption of selenium in the illite/smectite mixtures; the model's predictions were consistent with the experimental adsorption data.

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.

Neoformation of clay in lateral root catchments of mallee eucalypts: a chemical perspective

Science.gov (United States)

Verboom, William H.; Pate, John S.; Aspandiar, Mehrooz

2010-01-01

Background and Aims A previous paper (Annals of Botany 103: 673–685) described formation of clayey pavements in lateral root catchments of eucalypts colonizing a recently formed sand dune in south-west Western Australia. Here chemical and morphological aspects of their formation at the site are studied. Methods Chemical and physical examinations of soil cores through pavements and sand under adjacent heath assessed build-up of salts, clay and pH changes in or below pavements. Relationships of root morphology to clay deposition were examined and deposits subjected to scanning electron microscopy and energy-dispersive X-ray analysis. Xylem transport of mineral elements in eucalypt and non-eucalypt species was studied by analysis of xylem (tracheal) sap from lateral roots. Key Results The columns of which pavements are composed develop exclusively on lower-tier lateral roots. Such sites show intimate associations of fine roots, fungal filaments, microbiota and clay deposits rich in Si, Al and Fe. Time scales for construction of pavements by eucalypts were assessed. Cores through columns of pavemented profiles showed gross elevations of bulk density, Al, Fe and Si in columns and related increases in pH, Mg and Ca status in lower profiles. A cutting through the dune exhibited pronounced alkalinity (pH 7–10) under mallee woodland versus acidity (pH 5–6·5) under proteaceous heath. Xylem sap analyses showed unusually high concentrations of Al, Fe, Mg and Si in dry-season samples from column-bearing roots. Conclusions Deposition of Al–Fe–Si-rich clay is pivotal to pavement construction by eucalypts and leads to profound chemical and physical changes in relevant soil profiles. Microbial associates of roots are likely to be involved in clay genesis, with parent eucalypts supplying the required key mineral elements and carbon sources. Acquisition of the Al and Fe incorporated into clay derives principally from hydraulic uplift from ground water via deeply

The nanophase iron mineral(s) in Mars soil

Science.gov (United States)

Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

1993-01-01

A series of surface-modified clays containing nanophase (np) iron oxide/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these "Mars-soil analogs" were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging, specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The clay acted as an effective matrix, both chemically and sterically, preventing the major part of the synthesized iron oxides from ripening, i.e., growing and developing larger crystals. The precipitated iron oxides appear as isodiametric or slightly elongated particles in the size range 1-10 nm, having large specific surface area. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxy mineral such as "green rust," or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable maghemite (gamma-Fe2O3) by mild heat treatment and then to nanophase hematite (alpha-Fe2O3) by extensive heat treatment. After mild heating, the iron-enriched clay became slightly magnetic, to the extent that it adheres to a hand-held magnet, as was observed with Mars soil. The chemical reactivity of the iron-enriched clays strongly resembles, and offers a plausible mechanism

Mineralogical and Micro-fabric investigation of the Sandy Facies of Opalinus Clay (Mont Terri)

International Nuclear Information System (INIS)

Kaufhold, Annette; Siegesmund, Siegfried; Dohrmann, Reiner; Graesle, Werner; Plischke, Ingo

2013-01-01

In the field of geological disposal of radioactive waste in many countries argillaceous formations are considered as potential host rock. For the understanding of the long-term behaviour of clay host rock, it is important to understand the interaction between mechanical behaviour, micro-fabric, and mineral composition. Previous publications showed that particularly the carbonate content and the arrangement of the carbonate grains (as cement in the matrix or as shells) determines the mechanical strength of Opalinus Clay and Callovo-Oxfordian Clay specimens, respectively. Klinkenberg et al. (2009) studied the shaly facies of Opalinus Clay, however, the actual deposit is planned to be built in the sandy facies of Opalinus Clay. The aim of the present study is to investigate the relation between micro-fabric, mineral composition, and mechanical properties of different samples derived from the sandy facies (BLT-A2). Image analysis showed that the carbonates in the sandy facies mainly occur as 1) matrix which in turn acts as cement. Carbonates also occur 2) in the fine sand fraction and 3) biogenic carbonates as traces. The carbonates of the sandy facies, therefore, appear to be similar to the carbonates of the Callovo-Oxfordian Clay with respect to their possible influence on failure strength. The mechanical testing showed that the shear strength increases with increasing carbonate content. This phenomenon was also observed for the samples of the Callovo-Oxfordian Clay, while the opposite relation was found for the shaly facies of the Opalinus Clay. Preliminary results presented here, indicate that the sandy facies (drilling BLT-A2) and Callovo-Oxfordian Clay show similar mechanical properties - in detail: 1) Micro-fabric: carbonates predominate in the matrix, 2) Mineralogy: high carbonate content and 3) Mechanical testing: shear strength increases with increasing carbonate content, where the type of carbonates which controls the increase of strength has to be

Focusing on clay formation as host media of HLW geological disposal in China

International Nuclear Information System (INIS)

Zheng Hualing; Chen Shi; Sun Donghui

2007-01-01

Host medium is vitally important for safety for HLW geological disposal. Chinese HLW disposal effort in the past decades were mainly focused on granite formation. However, the granite formation has fatal disadvantage for HLW geological disposal. This paper reviews experiences gained and lessons learned in the international community and analyzes key factors affecting the site selection. It is recommended that clay formation should be taken into consideration and additional effort should be made before decision making of host media of HLW disposal in China. (authors)

Application of clay minerals from Cayo Guan, Cuba, as sorbents of heavy metals and ceramic raw materials

International Nuclear Information System (INIS)

Fonseca, D.; Barba, F.; Callejas, P.; Recio, P.

2012-01-01

It has been studied by Analysis Heating Microscope Optical the behaviour of some kaolinitic clays from a reservoir of Cayo Guan rich in iron oxides and low silica content proving to be a refractory materials whose softening appears after 1500 degree centigrade. It has obtained the workability diagram of the different clay minerals calculating the plasticity by the method of Casagrande spoon; only one of the samples is in the area suitable for extrusion. Vitrification diagrams report that the capacity of water absorption is 2 +, Cr 3 +. The results of the immobilization of these elements have been compared with those obtained with thermally activated vermiculite at 800 degree centigrade, showing that the treated samples show sorption of both cadmium and chromium below the vermiculite, but the non-treated ones are suitable to remove chromium; this is because these clays do not contain in its composition exchangeable ions (Ca 2 +, Mg 2 +, Na + , K + ), and even if they are chemically activated only the presence of Fe ions is which produces form bindings (Cr x .Fe 1 -x) (OH) 3 which favor Cr sorption. (Author) 26 refs.

Quorum Sensing Disruption in Vibrio harveyi Bacteria by Clay Materials.

Science.gov (United States)

Naik, Sajo P; Scholin, Jonathon; Ching, San; Chi, Fang; Herpfer, Marc

2018-01-10

This work describes the use of clay minerals as catalysts for the degradation of quorum sensing molecule N-(3-oxooctanoyl)-dl-homoserine lactone. Certain clay minerals as a result of their surface properties and porosity can catalytically degrade the quorum sensing molecule into smaller fragments. The disruption of quorum sensing by clay in a growing Gram-negative Vibrio harveyi bacteria culture was also studied by monitoring luminescence and population density of the bacteria, wherein quenching of bacterial quorum sensing activity was observed by means of luminescence reduction. The results of this study show that food-grade clays can be used as biocatalysts in disrupting bacterial activity in various media.

COMPOSITION OF MINERAL PHASES OF THE GHIDIRIM DIATOMITE

Directory of Open Access Journals (Sweden)

Vasile Rusu

2007-06-01

Full Text Available Studies of the mineralogical composition of diatomite from the Ghidirim location of RM, as well as of the extracted clay phase are presented. The mineral phase of the diatomite contains a number of clay minerals, like montmorillonite (in a mixture with insignificant quantities of slightly chloritized montmorillonite, illite and kaolinite. Diatomite contains also non-clay components as fine-dispersed quartz and amorphous material, the more probable sources of which are opal, amorphous alumosilicates, aluminum and iron hydroxides. The applied procedure for separation of clay fractions by sizing settling in liquid media proves to be very useful, enabling possibilities for more accurate identification of the clay constituents of diatomic material. Procedure allows to separate very clean clay fraction especially rich in montmorillonite, which can be utilized itself as mineral adsorbent for practical purposes.

Adsorption capacity of methylene blue, an organic pollutant, by montmorillonite clay

KAUST Repository

Feddal, I.; Ramdani, Amina; Taleb, Safia; Gaigneaux, E. M.; Batis, Narjè s Harrouch; Ghaffour, NorEddine

2013-01-01

The isotherms and kinetics of the adsorption of a cationic dye in aqueous solution, methylene blue, on a local Algerian montmorillonite clay mineral (raw, sodium and thermally activated at 300 and 500°C) were determined experimentally. Various parameters influencing the adsorption were optimized, mainly solid-liquid contact time, mass of adsorbent, initial concentration of dye, pH of the solution and temperature. Results showed that the adsorption kinetics were fast: 30 min for the raw clay mineral, and 20 min for sodium clay mineral (SC) and thermally activated at 300°C, whereas with the clay mineral calcined at 500°C, the equilibrium was reached after 150 min only. The maximum adsorption capacity was reached at pH 6.6. Results deducted from the adsorption isotherms also showed that the retention follows the Langmuir model. In addition, it was found that the kinetics were in the order of 2 (K = 2.457 × 106 g/mg.h) for sodium clay and were limited by an intra-particle diffusion. SC was found to be a better adsorbent to remove methylene blue from industrial wastewater. © 2013 Balaban Desalination Publications. All rights reserved.

Adsorption capacity of methylene blue, an organic pollutant, by montmorillonite clay

KAUST Repository

Feddal, I.

2013-11-19

The isotherms and kinetics of the adsorption of a cationic dye in aqueous solution, methylene blue, on a local Algerian montmorillonite clay mineral (raw, sodium and thermally activated at 300 and 500°C) were determined experimentally. Various parameters influencing the adsorption were optimized, mainly solid-liquid contact time, mass of adsorbent, initial concentration of dye, pH of the solution and temperature. Results showed that the adsorption kinetics were fast: 30 min for the raw clay mineral, and 20 min for sodium clay mineral (SC) and thermally activated at 300°C, whereas with the clay mineral calcined at 500°C, the equilibrium was reached after 150 min only. The maximum adsorption capacity was reached at pH 6.6. Results deducted from the adsorption isotherms also showed that the retention follows the Langmuir model. In addition, it was found that the kinetics were in the order of 2 (K = 2.457 × 106 g/mg.h) for sodium clay and were limited by an intra-particle diffusion. SC was found to be a better adsorbent to remove methylene blue from industrial wastewater. © 2013 Balaban Desalination Publications. All rights reserved.

Effects of natural increase in temperature on clay formations and determination of the course and the effects of geothermal fluids

International Nuclear Information System (INIS)

Polizzano, C.; Benvegnu, F.; Giannotti, G.; Brandimarte, U.

1986-01-01

The behaviour of clay cover towards the geothermal fluids rising up to the surface may represent an excellent natural analogue of the potential migration processes from deep waste repositories in clay formations. The ENEA is conducting research in an appropriate area near M. Amiata in southern Tuscany in order to contribute to solving the problem of the expected impermeability of clay formations. Geothermal fields may namely give an opportunity of studying a case of clay behaviour at a scale corresponding to size and time considered in waste disposal. In the considered area a relevant geothermal field is still active. A clay complex represents the impermeable cover of the local geothermal field. Several endogenous phenomena indicate the preferential ways of migrations of fluids from the basement throughout the cover. The data obtained by the present research prove that the upward flow of fluids, is possible only in the points of reduced thickness of the cover where very important faulting or granulometric discontinuity occur. This situation typically occurs at the border and not in the central part of the clay basins

The acid solubility test of clay mineral under microwave

International Nuclear Information System (INIS)

Zheng Ying; Niu Yuqing; Wu Peisheng; Niu Xuejun

2001-01-01

The acid solubility test of Al 3+ in clay from some uranium ores under microwave is introduced. The result shows that the concentration of Al 3+ in solution and the acid consumption increase rapidly under microwave comparing with normal leaching condition. It is infeasible to adopt microwave slacking method for intensively leaching uranium from uranium ore containing more clay

Evaluation of Used Fuel Disposition in Clay-Bearing Rock

Energy Technology Data Exchange (ETDEWEB)

Jove-Colon, Carlos F. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Weck, Philippe F. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Hammond, Glenn Edward [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Kuhlman, Kristopher L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Zheng, Liange [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Rutqvist, Jonny [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Kim, Kunhwi [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Houseworth, James [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Caporuscio, Florie Andre [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Cheshire, Michael [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Palaich, Sarah [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Norskog, Katherine E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Wolery, Thomas J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Jerden, James L. [Argonne National Lab. (ANL), Argonne, IL (United States); Copple, Jacqueline M. [Argonne National Lab. (ANL), Argonne, IL (United States); Cruse, Terry [Argonne National Lab. (ANL), Argonne, IL (United States); Ebert, William L. [Argonne National Lab. (ANL), Argonne, IL (United States)

2015-09-04

Deep geological disposal of nuclear waste in clay/shale/argillaceous rock formations has received much consideration given its desirable attributes such as isolation properties (low permeability), geochemically reduced conditions, slow diffusion, sorbtive mineralogy, and geologically widespread (Jové Colón et al., 2014). There is a wealth of gained scientific expertise on the behavior of clay/shale/ argillaceous rock given its focus in international nuclear waste repository programs that includes underground research laboratories (URLs) in Switzerland, France, Belgium, and Japan. Jové Colón et al. (2014) have described some of these investigative efforts in clay rock ranging from site characterization to research on the engineered barrier system (EBS). Evaluations of disposal options that include nuclear waste disposition in clay/shale/argillaceous rock have determined that this host media can accommodate a wide range of waste types. R&D work within the Used Fuel Disposition Campaign (UFDC) assessing thermal effects and fluid-mineral interactions for the disposition of heat-generating waste have so far demonstrated the feasibility for the EBS and clay host rock to withstand high thermal loads. This report represents the continuation of disposal R&D efforts on the advancement and refinement of coupled Thermal-Hydrological-Mechanical-Chemical (THMC), hydrothermal experiments on clay interactions, used fuel degradation (source term), and thermodynamic modeling and database development. The development and implementation of a clay/shale/argillite reference case described in Jové Colón et al. (2014) for FY15 will be documented in another report (Mariner et al. 2015) – only a brief description will be given here. This clay reference case implementation is the result of integration efforts between the GDSA PA and disposal in argillite work packages. The assessment of sacrificial zones in the EBS is being addressed through experimental work along with 1D reactive

Pentachlorophenol radical cations generated on Fe(III)-montmorillonite initiate octachlorodibenzo-p-dioxin formation in clays: DFT and FTIR studies

Science.gov (United States)

Gu, Cheng; Liu, Cun; Johnston, Cliff T.; Teppen, Brian J.; Li, Hui; Boyd, Stephen A.

2011-01-01

Octachlorodibenzodioxin (OCDD) forms spontaneously from pentachlorophenol (PCP) on the surfaces of Fe(III)-saturated smectite clay (1). Here, we used in situ FTIR methods and quantum mechanical calculations to determine the mechanism by which this reaction is initiated. As the clay was dehydrated, vibrational spectra showed new peaks that grew and then reversibly disappeared as the clay rehydrated. First principle DFT calculations of hydrated Fe-PCP clusters reproduced these transient FTIR peaks when inner-sphere complexation and concomitant electron transfer produced Fe(II) and PCP radical cations. Thus, our experimental (FTIR) and theoretical (quantum mechanical) results mutually support the hypothesis that OCDD formation on Fe-smectite surfaces is initiated by the reversible formation of metastable PCP radical cations via single electron transfer from PCP to Fe(III). The negatively charged clay surface apparently selects for this reaction mechanism by stabilizing PCP radical cations. PMID:21254769

Homogeneity vs. Heterogeneity of Porosity in Boom Clay

International Nuclear Information System (INIS)

Hemes, Susanne; Desbois, Guillaume; Urai, Janos L.; De Craen, Mieke; Honty, Miroslav

2013-01-01

Microstructural investigations on Boom Clay at nano- to micrometer scale, using BIB-SEM methods, result in porosity characterization for different mineral phases from direct observations on high resolution SE2-images of representative elementary areas (REAs). High quality, polished surfaces of cross-sections of ∼ 1 mm 2 size were produced on three different samples from the Mol-Dessel research site (Belgium). More than 33,000 pores were detected, manually segmented and analyzed with regard to their size, shape and orientation. Two main pore classes were defined: Small pores (< 500 nm (ED)) within the clay matrices of samples and =big' pores (> 500 nm (ED)) at the interfaces between clay and non-clay mineral (NCM) grains. Samples investigated show similar porosities regarding the first pore-class, but differences occur at the interfaces between clay matrix and NCM grains. These differences were interpreted to be due to differences in quantitative mineralogy (amount of non-clay mineral grains) and grain-size distributions between samples investigated. Visible porosities were measured as 15 to 17 % for samples investigated. Pore-size distributions of pores in clay are similar for all samples, showing log-normal distributions with peaks around 60 nm (ED) and more than 95 % of the pores being smaller than 500 nm (ED). Fitting pore-size distributions using power-laws with exponents between 1.56 and 1.7, assuming self-similarity of the pore space, thus pores smaller than the pore detection resolution following the same power-laws and using these power-laws for extrapolation of pore-size distributions below the limit of pore detection resolution, results in total estimated porosities between 20 and 30 %. These results are in good agreement with data known from Mercury Porosimetry investigations (35-40 % porosity) and water content porosity measurements (∼ 36 %) performed on Boom Clay. (authors)

The Composition and Physical Properties of Some Clays of Cross ...

African Journals Online (AJOL)

... and quartz as the main subsidiary non-clay mineral. The high plasticity index of the clays corresponds to the more transported clays of the tertiary- to –recent environment. The percentage of linear shrinkage varied from 11-16% with the lowest shrinkage (11%), having the coarsest features. Silica (SiO2) content of the clays ...

The geochemical behaviour of selenium in the Boom Clay system - a XANES and EXAFS study

International Nuclear Information System (INIS)

2S, KULeuven, B-3001Leuven (Belgium))" data-affiliation=" (Center for surface Chemistry and Catalysis - M2S, KULeuven, B-3001Leuven (Belgium))" >Breynaert, Eric; 2S, KULeuven, B-3001Leuven (Belgium))" data-affiliation=" (Center for surface Chemistry and Catalysis - M2S, KULeuven, B-3001Leuven (Belgium))" >Dom, Dirk; 2S, KULeuven, B-3001Leuven (Belgium))" data-affiliation=" (Center for surface Chemistry and Catalysis - M2S, KULeuven, B-3001Leuven (Belgium))" >Vancluysen, Jacqueline; 2S, KULeuven, B-3001Leuven (Belgium))" data-affiliation=" (Center for surface Chemistry and Catalysis - M2S, KULeuven, B-3001Leuven (Belgium))" >Kirschhock, Christine E.A.; 2S, KULeuven, B-3001Leuven (Belgium))" data-affiliation=" (Center for surface Chemistry and Catalysis - M2S, KULeuven, B-3001Leuven (Belgium))" >Maes, Andre; Scheinost, Andreas C.

2010-01-01

Document available in extended abstract form only. In Belgium, the Boom Clay formation is studied as a reference host formation for the geological disposal of high-level and long-lived radioactive waste for more than 30 years. This formation mainly consists of mixed clay minerals (illite, inter-stratified illite-smectite), pyrite and immobile and dissolved natural organic matter. Since it provides good sorption capacities, very low permeability, and chemically reducing conditions due to the presence of pyrite (FeS 2 ), the Boom clay formation itself is considered to be the main barrier preventing radionuclide migration from the geological repository. Within this concept for geological storage Se 79 has been identified as one of the critical elements contributing to the final dose to man. Although the sorption and migration behaviour of Se in the Boom Clay system has been thoroughly studied, the speciation of Se in the Boom Clay system has never been identified spectroscopically. In all previous studies, the interpretation of the behaviour of Se in Boom Clay conditions has always been based on circumstantial evidence such as solubility measurements or comparison with the spectroscopically identified speciation of Se in model systems. Based on the XANES analysis, selenite is transformed into Se 0 confirming the previously proposed reduction of selenite in the Boom Clay system. Combination of the mass-balance for Se with the results from linear combination analysis of the XANES spectra provided new evidence for the sorption-reduction mechanism proposed to explain the interaction between Se(IV) and the BC solid phase. In addition, evidence was found that that the fate of Se(IV) in the BC system is completely dominated by its interaction with pyrite present in the Boom Clay. The combined EXAFS analysis of Se in Se 0 reference phases (hexagonal, monoclinic, Se-loaded pyrite) allowed to elucidate further details on the short-range structure of the reaction products formed

On the origin of mixed-layered clay minerals from the San Andreas Fault at 2.5-3 km vertical depth (SAFOD drillhole at Parkfield, California)

Science.gov (United States)

Schleicher, A. M.; Warr, L. N.; van der Pluijm, B. A.

2009-02-01

A detailed mineralogical study is presented of the matrix of mudrocks sampled from spot coring at three key locations along the San Andreas Fault Observatory at depth (SAFOD) drill hole. The characteristics of authigenic illite-smectite (I-S) and chlorite-smectite (C-S) mixed-layer mineral clays indicate a deep diagenetic origin. A randomly ordered I-S mineral with ca. 20-25% smectite layers is one of the dominant authigenic clay species across the San Andreas Fault zone (sampled at 3,066 and 3,436 m measured depths/MD), whereas an authigenic illite with ca. 2-5% smectite layers is the dominant phase beneath the fault (sampled at 3,992 m MD). The most smectite-rich mixed-layered assemblage with the highest water content occurs in the actively deforming creep zone at ca. 3,300-3,353 m (true vertical depth of ca. 2.7 km), with I-S (70:30) and C-S (50:50). The matrix of all mudrock samples show extensive quartz and feldspar (both plagioclase and K-feldspar) dissolution associated with the crystallization of pore-filling clay minerals. However, the effect of rock deformation in the matrix appears only minor, with weak flattening fabrics defined largely by kinked and fractured mica grains. Adopting available kinetic models for the crystallization of I-S in burial sedimentary environments and the current borehole depths and thermal structure, the conditions and timing of I-S growth can be evaluated. Assuming a typical K+ concentration of 100-200 ppm for sedimentary brines, a present-day geothermal gradient of 35°C/km and a borehole temperature of ca. 112°C for the sampled depths, most of the I-S minerals can be predicted to have formed over the last 4-11 Ma and are probably still in equilibrium with circulating fluids. The exception to this simple burial pattern is the occurrence of the mixed layered phases with higher smectite content than predicted by the burial model. These minerals, which characterize the actively creeping section of the fault and local thin film

Clay vein and its implication for uranium exploration activity in the northern part of the Alligator Rivers Uranium Field, northern Australia

International Nuclear Information System (INIS)

Sasao, Eiji

2003-01-01

Clay veins have been found by uranium exploration drilling around the Black Rock uranium prospect in the northern part of the alligator Rivers Uranium Field (ARUF), northern Australia. The mineralogical and chemical features are described to clarify relations with uranium mineralization, because it is not accompanied by uranium mineralization. X-ray diffraction and chemical analysis for major elements indicate that the clay vein consists mainly of chlorite (clinochlore to ferroan clinochlore) and lesser mica clay mineral (t-1M dominant). The clay vein is compared with the clay alteration zone around the uranium deposits in ARUF in terms of mode of occurrence, mineral and chemical compositions. Mineral composition of the clay vein is only in accordance with that of the inner alteration halo of the clay alteration zone. It is, however, different from mineral composition of the outer alteration halo in terms of lack of Fe chlorite in the clay vein. Chemical composition of the clay vein is similar to that of the clay alteration zone, except for lack in the vein of high iron content which is observed in some samples of the alteration zone. As a whole, the feature of the clay vein corresponds to the inner alteration zone around the uranium deposit in ARUF. The mode of occurrence of the clay vein is very different from that of the clay alteration zone. Mode of occurrence, and mineral and chemical compositions of the clay vein resemble a chlorite vein in the Lower to Middle Proterozoic sandstone above the Jabiluka deposit, one of major uranium deposit in the ARUF. Because of the similarity between the clay and the chlorite veins, the clay vein is regarded as marginal facies of an alteration zone. The fluid that formed the clay vein is estimated to have been oxidized, because of the existence of hematite and ubiquitous Mg chlorite. This nature is in accordance with the mineralizing fluid that formed the inner alteration zone in the Nabarlek deposit. In conclusion, the vein

Performance assessment of an alpha waste deposit in a clay formation

International Nuclear Information System (INIS)

Quercia, F.; D'Alessandro, M.; Saltelli, A.

1987-01-01

The probabilistic code LISA (Long term Isolation Safety Assessment) has been used to assess the risk related to the disposal of alpha waste in a geological formation. The code has been modified to take into account waste form properties and leaching processes pertinent to alpha waste produced at fuel reprocessing plants. The exercise refers to a repository in a deep clay formation located at Harwell (U.K.) where some hydrogeological data were available. Radionuclide migration through repository and geological barriers has been simulated together with biosphere contamination. Results of the assessment are presented as dose rate (or risk) distributions; a sensitivity analysis on input parameters has been performed

Going through the wine fining: Intimate dialogue between organics and clays.

Science.gov (United States)

Trigueiro, Pollyana; Pedetti, Silvia; Rigaud, Baptiste; Balme, Sebastien; Janot, Jean-Marc; Dos Santos, Ieda M G; Gougeon, Régis; Fonseca, Maria G; Georgelin, Thomas; Jaber, Maguy

2018-06-01

Wine chemistry inspires and challenges with its complexity and intriguing composition. In this context, the composites based on the use of a model protein, a polyphenol of interest and montmorillonite in a model hydroalcoholic solution have been studied. A set of experimental characterization techniques highlighted the interactions between the organic and the inorganic parts in the composite. The amount of the organic part was determined by ultraviolet-visible (UV-VIS) and thermal analysis. X-ray diffraction (XRD) and transmission electronic microscopy (TEM) informed about the stacking/exfoliation of the layers in the composites. Vibrational and nuclear magnetic resonance spectroscopies methods stressed on the formation of a complex between the protein and the polyphenol before adsorption on the clay mineral. The mobility/rigidity of the organic parts were determined by fluorescence time resolved spectroscopy. Changes in the secondary structure of the protein occured upon complexation with polyphenol on clay mineral due to strong interactions. Although not representating faithfully enological conditions, these results highlight the range and nature of mechanisms possibly involved in wine fining. Copyright © 2018 Elsevier B.V. All rights reserved.

Clay formation and metal fixation during weathering of coal fly ash

International Nuclear Information System (INIS)

Zevenbergen, C.; Bradley, J.P.; Reeuwijk, L.P. Van; Shyam, A.K.; Hjelmar, O.; Comans, R.N.J.

1999-01-01

The enormous and worldwide production of coal fly ash cannot be durably isolated from the weathering cycle, and the weathering characteristics of fly ash must be known to understand the long-term environmental impact. The authors studied the weathering of two coal fly ashes and compared them with published data from weathered volcanic ash, it's closest natural analogue. Both types of ash contain abundant aluminosilicate glass, which alters to noncrystalline clay. However, this study reveals that the kinetics of coal fly ash weathering are more rapid than those of volcanic ash because the higher pH of fresh coal fly ash promotes rapid dissolution of the glass. After about 10 years of weathering, the noncrystalline clay content of coal fly ash is higher than that of 250-year-old volcanic ash. The observed rapid clay formation together with heavy metal fixation imply that the long-term environmental impact of coal fly ash disposal may be less severe and the benefits more pronounced than predicted from previous studies on unweathered ash. Their findings suggest that isolating coal fly ash from the weathering cycle may be counterproductive because, in the long-term under conditions of free drainage, fly ash is converted into fertile soil capable of supporting agriculture

Formation of secondary minerals in a lysimeter approach - A mineral-microbe interaction

Science.gov (United States)

Schäffner, F.; Merten, D.; De Giudici, G.; Beyer, A.; Akob, D. M.; Ricci, P. C.; Küsel, K.; Büchel, G.

2012-04-01

Heavy metal contamination of large areas due to uranium mining operations poses a serious long-term environmental problem. In the Ronneburg district (eastern Thuringia, Germany), leaching of low grade uranium bearing ores (uranium content metals, especially Cd, Ni, Co, Cu and Zn due to a residual contamination even after remediation efforts. To reveal the processes of secondary mineral precipitation in the field a laboratory lysimeter approach was set up under in situ-like conditions. Homogenized soil from the field site and pure quartz sand were used as substrates. In general, in situ measurements of redox potentials in the substrates showed highly oxidizing conditions (200-750 mV). Water was supplied to the lysimeter from below via a mariottés bottle containing contaminated groundwater from the field. Evaporation processes were allowed, providing a continuous flow of water. This led to precipitation of epsomite and probably aplowite on the top layer of substrate, similar to what is observed in field investigations. After 4 weeks, the first iron and manganese bearing secondary minerals became visible. Soil water samples were used to monitor the behaviour of metals within the lysimeter. Saturation indices (SI) for different secondary minerals were calculated with PHREEQC. The SI of goethite showed oversaturation with respect to the soil solution. SEM-EDX analyses and IR spectroscopy confirmed the formation of goethite. Geochemical data revealed that goethite formation was mainly dominated by Eh/pH processes and that heavy metals, e.g. Zn and U, could be enriched in this phase. Although Eh/pH data does not support formation of manganese minerals, Mn(II)-oxidizing bacteria (MOB) could be isolated from field soil samples, supporting the fact that microorganisms may influence this natural attenuation process. Laser ablation ICP-MS data reveal accumulation of manganese in MOB biomass on Mn(II)-containing agar plates. Furthermore, it was possible to show the importance

Immobilization of aqueous radioactive cesium wastes by conversion to aluminosilicate minerals

International Nuclear Information System (INIS)

Barney, G.S.

1975-05-01

Radioactive cesium (primarily 137 Cs) is a major toxic constituent of liquid wastes from nuclear fuel processing plants. Because of the long half-life, highly penetrating radiation, and mobility of 137 Cs, it is necessary to convert wastes containing this radioisotope into a solid form which will prevent movement to the biosphere during long-term storage. A method for converting cesium wastes to solid, highly insoluble, thermally stable aluminosilicate minerals is described. Aluminum silicate clays (bentonite, kaolin, or pyrophyllite) or hydrous aluminosilicate gels are reacted with basic waste solutions to form pollucite, cesium zeolite (Cs-D), Cs-F, cancrinite, or nepheline. Cesium is trapped in the aluminosilicate crystal lattice of the mineral and is permanently immobilized. The identity of the mineral product is dependent on the waste composition and the SiO 2 /Al 2 O 3 ratio of the clay or gel. The stoichiometry and kinetics of mineral formation reactions are described. The products are evaluated with respect to leachability, thermal stability, and crystal morphology. (U.S.)

Sorption and fixation of large cations by shale formations

International Nuclear Information System (INIS)

Brindley, G.W.

1977-01-01

Large cations such as Cs + are preferentially sorbed and partially fixed by fine-grained 2 : 1 type layer silicates such as micas, vermiculites, smectites and various mixed-layer minerals. Since these minerals are common constituents of many shale formations, these formations may provide suitable location for the burial of radioactive waste containers. However, the usual investigations of cation sorption and fixation must be extended to the conditions likely to develop in the vicinity of buried radioactive waste. Prior to possible leakage from buried containers, elevated temperatures around the burial site will develop leading to hydrothermal modification of the surrounding mineralogy. A range of temperature and of mineralogy must be envisaged. If and when leakage occurs, an outward diffusion of radioactive ions will occur by solvation in the fluids in the shale. The ratio of radioactive ions/normal ions will diminish outwards from the source. At near distances from the source high temperature modifications of the clay minerals and high concentrations of radioactive cations may lead to saturation of the fixation capacity. At greater distances, little or no thermal modification of the clay minerals and lower concentrations of ions will permit maximum sorption and fixation

Clay particles as binder for earth buildings materials: a fresh look into rheology of dense clay suspensions

Science.gov (United States)

Landrou, Gnanli; Brumaud, Coralie; Habert, Guillaume

2017-06-01

In the ceramic industry and in many sectors, clay minerals are widely used. In earthen construction technique, clay plays a crucial role in the processing. The purpose of this research is to understand and modify the clay properties in earth material to propose an innovative strategy to develop a castable earth-based material. To do so, we focused on the modification of clay properties at fresh state with inorganic additives. As the rheological behaviour of clays is controlled by their surface charge, the addition of phosphate anion allows discussing deep the rheology of concentrated clay suspensions. We highlighted the thixotropic and shear thickening behaviour of a dispersed kaolinite clay suspensions. Indeed, by adding sodium hexametaphosphate the workability of clay paste increases and the behaviour is stable during time after a certain shear is applied. Moreover, we stress that the aging and the shift in critical strain in clay system are due to the re-arrangement of clay suspension and a decrease of deformation during time. The understanding of both effect: thixotropy and aging are crucial for better processing of clay-based material and for self-compacting clay concrete. Yet, studies need to pursue to better understand the mechanism.

Clays causing adhesion with tool surfaces during mechanical tunnel driving

Science.gov (United States)

Spagnoli, G.; Fernández-Steeger, T.; Stanjek, H.; Feinendegen, M.; Post, C.; Azzam, R.

2009-04-01

During mechanical excavation with a tunnel boring machine (TBM) it is possible that clays stick to the cutting wheel and to other metal parts. The resulting delays in the progress of construction work, cause great economic damage and often disputes between the public awarding authorities and executing companies. One of the most important factors to reduce successfully the clay adhesion is the use of special polymers and foams. But why does the clay stick to the metal parts? A first step is to recognize which kind of clay mineralogy shows serious adhesion problems. The mechanical properties of clay and clay suspensions are primarily determined by surface chemistry and charge distribution at the interfaces, which in turn affect the arrangement of the clay structure. As we know, clay is a multi-phase material and its behaviour depends on numerous parameters such as: clay mineralogy, clay fraction, silt fraction, sand fraction, water content, water saturation, Atterberg limits, sticky limit, activity, cation exchange capacity, degree of consolidation and stress state. It is therefore likely that adhesion of clay on steel is also affected by these clay parameters. Samples of clay formations, which caused problems during tunnel driving, will be analyzed in laboratory. Mineralogical analyses (diffractometry, etc.) will be carried out to observe which minerals are responsible for adherence problems. To manipulate the physical properties, batch tests will be carried out in order to eliminate or reduce the adhesion on tool surfaces through variation of the zeta potential. Second step is the performance of vane shear tests on clay samples. Different pore fluid (distilled water, pure NaCl solution, ethanol and methanol) will be used to study the variation of the mechanical behaviour of clay depending on the dielectric constant of the fluids. This project is funded by the German Federal Ministry of Education and Research (BMBF) and the DFG (German Research Foundation) in the

Geotechnical aspects of tunnel construction in deep clay formations for radioactive waste disposal

International Nuclear Information System (INIS)

De Moor, E.K.

1987-01-01

The significant factors affecting the construction of tunnels in deep clay formations for radioactive waste disposal were outlined. Two aspects of tunneling were discussed; the feasibility of tunnel construction and changes in pore water pressure that might occur with time. Some results of model tunnel tests and analyses were presented. (U.K.)

Biogeochemical processes in a clay formation in situ experiment: Part B - Results from overcoring and evidence of strong buffering by the rock formation

Energy Technology Data Exchange (ETDEWEB)

Koroleva, M. [Institute of Geological Sciences, University of Bern, Baltzerstrasse 3, CH-3012 Bern (Switzerland); Lerouge, C. [BRGM, French Geological Survey, 3 Avenue Claude Guillemin, B.P. 36009, 45060 Orleans Cedex 2 (France); Maeder, U., E-mail: urs.maeder@geo.unibe.ch [Institute of Geological Sciences, University of Bern, Baltzerstrasse 3, CH-3012 Bern (Switzerland); Claret, F.; Gaucher, E. [BRGM, French Geological Survey, 3 Avenue Claude Guillemin, B.P. 36009, 45060 Orleans Cedex 2 (France)

2011-06-15

Highlights: > A 5-year in situ porewater chemistry experiment in Opalinus Clay was overcored and examined. > A microbial perturbation induced sulfate reduction, pH decrease and alkalinity / P{sub CO2} increase. > Changes to mineralogy, isotopic composition and bulk properties could not be detected. > Precipitation of Fe-sulfides and carbonate occurred at the interface of the test interval. > The chemical perturbation was effectively buffered by the claystone's large capacity. - Abstract: An in situ Porewater Chemistry (PC) experiment in the Opalinus Clay formation was carried out at the Mont Terri underground rock laboratory (Jura Mountains, Switzerland) for a period of 5 a. A traced water with a composition close to that expected in the formation was continuously circulated and monitored in a packed-off borehole to achieve diffusive equilibration. An unwanted microbial perturbation changed the water composition, characterized by reduction of SO{sub 4} combined with increasing sulfide, increasing alkalinity, decreasing pH and increasing P(CO{sub 2}). In contrast, the main cations (Na, Ca, Mg) remained remarkably constant during the experiment, thus indicating the strong buffering of the formation via cation and proton exchange as well as carbonate dissolution/precipitation reactions. After 5 a, the 4.5 m long vertical test interval was overcored and Opalinus Clay samples were analyzed along ca. 15 cm long radial profiles. The analytical investigations included mineralogy (XRD, SEM-EDX), bulk parameters (water content, density, C, S), cation exchange capacity and occupancy, aqueous leachates for Cl{sup -}, Br{sup -}, SO{sub 4}{sup 2-} and water and carbonate stable isotopes. Emphasis was put on best sample preparation and conservation techniques. Results show that the distribution of non-reactive tracers (Br{sup -} and {sup 2}H) follows the expected out/in-diffusion profiles compatible with the time-dependent boundary conditions in the test interval of the

Radiocesium sorption in relation to clay mineralogy of paddy soils in Fukushima, Japan

Energy Technology Data Exchange (ETDEWEB)

Nakao, Atsushi, E-mail: na_4_ka_triplochiton@kpu.ac.jp [Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Hangi-cho 1-5, Shimogamo, Sakyo-ku, Kyoto 606-8522 (Japan); Ogasawara, Sho [Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Hangi-cho 1-5, Shimogamo, Sakyo-ku, Kyoto 606-8522 (Japan); Sano, Oki; Ito, Toyoaki [Field Science Center, Graduate School of Agricultural Science, Tohoku University, Naruko-Onsen 232-3, Osaki, Miyagi 989-6711 (Japan); Yanai, Junta [Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Hangi-cho 1-5, Shimogamo, Sakyo-ku, Kyoto 606-8522 (Japan)

2014-01-01

Relationships between Radiocesium Interception Potential (RIP) and mineralogical characteristics of the clay fraction isolated from 97 paddy soils (Hama-dori, n = 25; Naka-dori, n = 36; Aizu, n = 36) in Fukushima Prefecture, Japan were investigated to clarify the mineralogical factors controlling the {sup 137}Cs retention ability of soils (half-life 30.1 y). Of all the fission products released by the Fukushima accident, {sup 137}Cs is the most important long-term contributor to the environmental contamination. The RIP, a quantitative index of the {sup 137}Cs retention ability, was determined for the soil clays. The composition of clay minerals in the soil clays was estimated from peak areas obtained using X-ray diffraction (XRD) analyses. The predominant clay mineral was smectite in soils from Hama-dori and Aizu, while this was variable for those from Naka-dori. Native K content of the soil clays was found to be an indicator of the amount of micaceous minerals. The average RIP for the 97 soil clays was 7.8 mol kg{sup −1}, and ranged from 2.4 mol kg{sup −1} to 19.4 mol kg{sup −1}. The RIP was significantly and positively correlated with native K content for each of the geographical regions, Hama-dori (r = 0.76, p < 0.001), Naka-dori (r = 0.43, p < 0.05), and Aizu (r = 0.76, P < 0.001), while it was not related to the relative abundance of smectite. The linear relationship between RIP and native K content not only indicate a large contribution of micaceous minerals to the {sup 137}Cs retention ability of the soil clays, but also could be used to predict the {sup 137}Cs retention ability of soil clays for other paddy fields in Fukushima and other areas. - Highlights: • RIP was measured for 97 paddy soils from Fukushima to assess {sup 137}Cs retention ability. • The dominant clay mineral was smectite, but this did not control RIP. • RIP was positively correlated with native K content. • Micaceous minerals were found to control the {sup 137}Cs retention

Clay minerals in sediments of Portuguese reservoirs and their significance as weathering products from over-eroded soils: a comparative study of the Maranhão, Monte Novo and Divor Reservoirs (South Portugal)

Science.gov (United States)

Fonseca, Rita M. F.; Barriga, Fernando J. A. S.; Conceição, Patrícia I. S. T.

2010-12-01

The Southern region of Portugal is subjected to several forms of over-erosion. Most leached products, mainly composed of fine particles containing nutrients, metals or pesticides, are easily transported by river flows. When these are hindered by a physical barrier such as a dam, the particulate load accumulates on the bottom of the reservoirs, often leading to a pronounced decrease of water quality. Bottom sediments from three reservoirs were subjected to grain-size analysis and a study of clay minerals by X-ray diffraction. Most sediments contain a diverse set of clay minerals, mostly illites, smectites, chlorites and kaolinites. The nature of the clay minerals reflects the nature of the parent rocks. During the cycles of transport and temporary deposition, they may undergo significant chemical and physical transformations, which lead to an increase of expandable properties and therefore, to a higher cationic exchange capacity, determining its important role as vehicles of environmental pollutants.

Measurement techniques for in situ stresses around underground constructions in a deep clay formation

Directory of Open Access Journals (Sweden)

Li X.L.

2010-06-01

Full Text Available Disposal in deep underground geological formations is internationally recognized as the most viable option for the long-term management of high-level radioactive waste. In Belgium, the Boom clay formation is extensively studied in this context, in particular at the 225 m deep HADES Underground Research Facility in Mol. A cost-effective design of deep underground structures requires an accurate assessment of the in situ stresses; a good estimation of these stresses is also essential when interpreting in situ experiments regarding the hydro-mechanical behaviour of the host formation. Different measurement techniques are available to provide data on the stress evolution and other mechanical properties of the geological formation. The measurement can be direct (measurement of total pressure, or it can be an indirect technique, deriving the stress from related quantities such as strain (changes in structural members. Most total stress measurements are performed through permanently installed sensors; also once-only measurements are performed through specific methods (e.g. pressuremeter. Direct measurement of the stress state is challenging due to the complex mechanical behaviour of the clay, and the fact that the sensor installation inevitably disturbs the original stress field. This paper describes ways to deal with these problems and presents the results obtained using different techniques at HADES.

Clays in natural and engineered barriers for radioactive waste confinement - 5. International meeting. Book of abstracts

International Nuclear Information System (INIS)

2012-10-01

The purpose of this fifth international meeting is to bring again together specialists in the different disciplines related to clays and clay minerals, with scientists from organizations engaged in disposal of radioactive waste in order to evaluate the progress of the research conducted in that field. Multidisciplinary approaches including geology, mineralogy, geochemistry, rheology, physics and chemistry of clay minerals and assemblages are required in order to provide a detailed characterization of the geological host formations considered for the disposal of radioactive waste and to assess the behaviour of engineered and natural barriers when submitted to various types of perturbations induced by such facilities. The evaluation of the performances of the natural barrier as well as of the impact of repository-induced disturbances upon the confinement properties of clay-rich geological formations constitute major objectives for the experimental programs being and/or to be conducted in underground research laboratories, for interpreting the subsequent scientific results, for modelling the long-term behaviour of radioactive waste repositories and carrying out safety assessment exercises. The meeting covers all the aspects of clay characterization and behaviour considered at various times and space scales relevant to confinement of radionuclides in clay from basic phenomenological processes description, to the global understanding of the performance and safety at repository and geological scales. Special emphasis will be put on the modelling of processes occurring at the mineralogical level within the clay barriers. The topics covered by the program of the meeting are also supposed to be coherent with the general objectives proposed within the Strategic Research Agenda elaborated through the Implementing Geological Disposal of Radioactive Waste Technology Platform (IGD-TP). In this context, the meeting will also offer a particular opportunity to present the more

CONTRAST IN CLAY MINERALOGY AND THEIR EFFECT ON ...

African Journals Online (AJOL)

a

Clay minerals reduced the porosity and permeability of the Permo-Triassic sandstones. .... Lower Triassic-Lias .... and show high birefringence around the grains. ..... It is a regime after effective burial depth in which the solubility of minerals.

Timing and conditions of clay fault gouge formation on the Naxos detachment (Cyclades, Greece)

Science.gov (United States)

Mancktelow, N.; Zwingmann, H.; Mulch, A.

2016-10-01

Clay fault gouge from the Naxos detachment (locally up to 1.0-1.5 m thick) is reported and dated for the first time. K-Ar ages on eight clay size fractions from the detachment and a minor fault in the immediate footwall have a narrow range, from 10.3 to 9.0 Ma, with an average of 9.7 ± 0.5 Ma (±1σ). These results are in excellent accord with regional and local age constraints, independently demonstrating the reliability of the method. Hydrogen δD values fall in the range -89 to -95‰, indicating interaction with infiltrating meteoric water during gouge formation, which is consistent with deposition of freshwater sediments in the hanging wall at the same time. Clay mineralogy in the detachment gouge is predominantly mixed layer illite-smectite with subordinate 1 M illite and kaolinite but without higher-temperature 2 M1 illite/mica. Clay fault gouge predominantly formed over a limited time and temperature range, potentially acting as a weak lubricant promoting movement on the Naxos detachment, with correspondingly rapid exhumation and cooling of the underlying footwall.

Interactions between fluids and natural clay rich sediments: experimental study in conditions simulating radioactive wastes underground storage

International Nuclear Information System (INIS)

Roubeuf, V.

2000-10-01

The behaviour of clay rich sediments, especially an argilite from Oxfordian of Haute-Marne, a siltite from Albian series of Marcoule (Gard) and a bentonite from Wyoming, were experimentally studied under physical-chemical conditions close of those of an underground radioactive waste storage. The several steps of the creation of the storage in deep formation were simulated experimentally, in particular: - the effect due to oxidation at ambient temperature and moisture degree related to the arrival of air in the gallery, was tested, especially the interaction between acid fluids generated at the micron-scale of the altered pyrite micro-site and the surrounding minerals of the sediment, - the alteration due to weathering (damping/drying cycles) to simulate the effect of a surface storage of the sediments, - and finally, water-rock interactions at 80 and 200 deg C, which reproduce the thermic stress induced by the deposit of type C radioactive containers (stage of re-hydration under thermic stress). The various simulations lead to rather similar behaviour of minerals in the sediment and solutions. Mineralogical, geochemical and crystallographic analyses show that most minerals in sediments are preserved with no evidence of mineral neo-formation. Nevertheless, the study by X-ray diffraction shows variations in the interlayer spacing in relation with modifications of the hydration states. Changes in the interlayer occupancy of the clays are due to cationic exchange of the sodium of the interlayer by the calcium issued from the dissolution of carbonate and gypsum dissolution. I/S like minerals crystal-chemistry generally display little changes in the tetrahedral and octahedral occupancy and a rather good stability of crystal structure. The cationic exchange capacity (CEC) of the clay sediment display un-significant variations: after the damping/drying cycles, the argilite of Haute-Marne has lost about 15 % of their bulk CEC and the effect of acid micro-environment at

Method for the determination of clay and mica concentrations in subsurface sandstone formations through radioactive logging

International Nuclear Information System (INIS)

Allen, L.S.

1984-01-01

A method is described for radioactivity well logging in a subsurface sandstone formation penetrated by a borehole. The invention relates particularly to clay and mica contents, which are determined from the natural gamma-ray activities. The natural sources of gamma radiation in the formation, are the trace elements thorium, uranium and potassium. (U.K.)

Understanding the acquisition and regulation mechanisms of the water chemistry in a clay formation: the CEC/ANDRA Archimede-argile project

International Nuclear Information System (INIS)

Merceron, T.; Mossmann, J.R.; Neerdael, B.; Canniere, P. de; Beaucaire, C.; Toulhoat, P.; Daumas, S.; Bianchi, A.; Christen, R.

1993-01-01

Clay formations are candidate host environments to high level radioactive waste repository. The radioelements could be partially released from the waste into the host geological formation after a very long time. Understanding behaviour of the natural chemical species is considered as a fundamental prerequisite before the disturbed system will be studied. Additional laboratory studies are also essential in order to forecast, by analogy, the behaviour of radioelements released from the radioactive waste repository. The ARCHIMEDE-ARGILE project has two main goals. The first is to gain an understanding of the mechanisms of acquisition and regulation of the water chemistry in a clay environment. This step is essential to predict both the behaviour and the migration in solution of artificial elements which are initially absent in the clay formation. The second is to test and validate in clay the measured physico chemical parameters which are the basis for the geochemical modelling of the behaviour of the natural and artificial radioelements. The paper presents the main results previously obtained on granitic waters and the research strategy established for the ARCHIMEDE project. (authors). 2 figs., 2 refs

Occurrence of tephra/volcanic tuff in the tertiary sediments of Himachal Himalaya from Tileli area, Mandi district, H.P.: implication for stratigraphy and uranium mineralization

International Nuclear Information System (INIS)

Pandey, Pradeep; Chabbra, Jyotsana; Joshi, G.B.; Parihar, P.S.

2014-01-01

Presence of Early Tertiary pyroclastic material (tephra) has been documented petrographically, for the first time, in the Mandi-Bilaspur Sector from Tileli area, Dharamsala basin of Himachal Pradesh. The tephra is reported from the red shale, identified as tuffaceous siltstone belonging to lower Dharamsala Formation that lies above the uraniferous sandstone body and occurs as thin layers of over 300m along the strike, close to the contact of lower and upper Dharamsala formations. The tuffaceous material shows crude but preferred orientation of minerals like biotite, muscovite, chlorite, clay, hematite and specularite. Various features indicating presence of tephra are, glass shards altered to clay but retaining 'U' shaped outline, spindle-shaped hematite with preferred orientation, spherical to sub-spherical clay and altered Fe oxide rich balls, clay groundmass with flow pattern, flaky minerals in association with clast depicting asymmetrical ramp structure. A zone of approximately 300 m length containing tuffaceous material has been established at Tileli overlying the uraniferous sandstone body. Identification of tephra at Tileli has significant implications as it enabled in demarcating the boundary between the upper and lower Dharamsala formations in central part of the basin in Bilaspur-Mandi Sector of HP Himalaya and also in guiding the uranium exploration programme in the lower Dharamsala Formation. (author)

Admissible thermal loading in geological formations. Consequences on radioactive waste disposal methods

International Nuclear Information System (INIS)

1982-01-01

For the final disposal of conditioned radioactive wastes clay formations have plasticity, low permeability and high sorption capacity in their favour. Their disadvantage lies in their thermal conductivity and moisture content. The aim of this document is to take stock of the state of the art pertaining to the thermal phenomena linked to the dispoasl of conditioned radioactive wastes. The study, limited to normal, non-accident operating conditions, considers vitrified wastes cast in metal containers and disposal of in an underground infrastructure built in clay. The composition and characteristics of clays can vary widely between formations and even between sites, since the nature and content of argillaceous and other minerals depend on age, sedimentation conditions, depth, origin of the sediments, etc. This study is therefore limited to a specific clay in a specific deposit, i.e., the Boom clay located at Mol beneath the CEN/SCK establishment

Inter-layered clay stacks in Jurassic shales

Science.gov (United States)

Pye, K.; Krinsley, D. H.

1983-01-01

Scanning electron microscopy in the backscattered electron mode is used together with energy-dispersive X-ray microanalysis to show that Lower Jurassic shales from the North Sea Basin contain large numbers of clay mineral stacks up to 150 microns in size. Polished shale sections are examined to determine the size, shape orientation, textural relationships, and internal compositional variations of the clays. Preliminary evidence that the clay stacks are authigenic, and may have formed at shallow burial depths during early diagenesis, is presented.

Online differentiation of mineral phase in aerosol particles by ion formation mechanism using a LAAP-TOF single-particle mass spectrometer

Science.gov (United States)

Marsden, Nicholas A.; Flynn, Michael J.; Allan, James D.; Coe, Hugh

2018-01-01

Mineralogy of silicate mineral dust has a strong influence on climate and ecosystems due to variation in physiochemical properties that result from differences in composition and crystal structure (mineral phase). Traditional offline methods of analysing mineral phase are labour intensive and the temporal resolution of the data is much longer than many atmospheric processes. Single-particle mass spectrometry (SPMS) is an established technique for the online size-resolved measurement of particle composition by laser desorption ionisation (LDI) followed by time-of-flight mass spectrometry (TOF-MS). Although non-quantitative, the technique is able to identify the presence of silicate minerals in airborne dust particles from markers of alkali metals and silicate molecular ions in the mass spectra. However, the differentiation of mineral phase in silicate particles by traditional mass spectral peak area measurements is not possible. This is because instrument function and matrix effects in the ionisation process result in variations in instrument response that are greater than the differences in composition between common mineral phases.In this study, we introduce a novel technique that enables the differentiation of mineral phase in silicate mineral particles by ion formation mechanism measured from subtle changes in ion arrival times at the TOF-MS detector. Using a combination of peak area and peak centroid measurements, we show that the arrangement of the interstitial alkali metals in the crystal structure, an important property in silicate mineralogy, influences the ion arrival times of elemental and molecular ion species in the negative ion mass spectra. A classification scheme is presented that allowed for the differentiation of illite-smectite, kaolinite and feldspar minerals on a single-particle basis. Online analysis of mineral dust aerosol generated from clay mineral standards produced mineral fractions that are in agreement with bulk measurements reported by

Clay particles as binder for earth buildings materials: a fresh look into rheology of dense clay suspensions

Directory of Open Access Journals (Sweden)

Landrou Gnanli

2017-01-01

Full Text Available In the ceramic industry and in many sectors, clay minerals are widely used. In earthen construction technique, clay plays a crucial role in the processing. The purpose of this research is to understand and modify the clay properties in earth material to propose an innovative strategy to develop a castable earth-based material. To do so, we focused on the modification of clay properties at fresh state with inorganic additives. As the rheological behaviour of clays is controlled by their surface charge, the addition of phosphate anion allows discussing deep the rheology of concentrated clay suspensions. We highlighted the thixotropic and shear thickening behaviour of a dispersed kaolinite clay suspensions. Indeed, by adding sodium hexametaphosphate the workability of clay paste increases and the behaviour is stable during time after a certain shear is applied. Moreover, we stress that the aging and the shift in critical strain in clay system are due to the re-arrangement of clay suspension and a decrease of deformation during time. The understanding of both effect: thixotropy and aging are crucial for better processing of clay-based material and for self-compacting clay concrete. Yet, studies need to pursue to better understand the mechanism.

Antimony(V) Adsorption by Variable-Charge Minerals

Science.gov (United States)

2013-10-01

6‒] and inner-sphere [≡SOSb(OH)5‒] adsorption mechanisms. In general, however, the models generated for single ligand systems required reoptimization...HCO3 and CO3 ) effectively desorbed Sb(V) from hydrous metal (Al and Fe) oxides, clay minerals, and Sb(V)-contaminated sediments, relative to the...temperatures (20- 22°C). 7 A well- crystallized Georgia kaolinite (KGa-1b) from the Source Clays Repository of The Clay Minerals Society (West Lafayette

Mud peeling and horizontal crack formation in drying clays

KAUST Repository

Style, Robert W.

2011-03-01

Mud peeling is a common phenomenon whereby horizontal cracks propagate parallel to the surface of a drying clay. Differential stresses then cause the layer of clay above the crack to curl up to form a mud peel. By treating the clay as a poroelastic solid, we analyze the peeling phenomenon and show that it is caused by the gradient in tensile stress at the surface of the clay, analogously to the spalling of thermoelastic materials. For a constant water evaporation rate at the clay surface we derive equations for the depth of peeling and the time of peeling as functions of the evaporation rate. Our model predicts a simple relationship between the radius of curvature of a mud peel and the depth of peeling. The model predictions are in agreement with the available experimental data. Copyright 2011 by the American Geophysical Union.

Geotechnical variability of permafrozen glaciomarine clays in Sdr. Strømfjord in Greenland

DEFF Research Database (Denmark)

Foged, Niels Nielsen; Ingeman-Nielsen, Thomas; Belmonte, Louise Josefine

2014-01-01

-going in the area at Strømfjordshavn. The C14 datings of marine shells collected on the marine clay terraces at level 300kPa. Clay minerals were weathered causing moderate to high activity and plasticity despite the formation age of only 7000 years. (b) The "River Bank Erosion Cut" 2 km east of the Airport Terminal...... level with Upper Marine Limit (UML) varying from +120 to +140m at the West Coast to +40 at Kangerlussuaq. This retreat is well documented through C14-dating in the local area near to Kangerlussuaq Airport related to Fjord Stages F2 (+60m/8300 y BC) and F3 (+40m/8100 y BC) and Mt. Keglen stage (+40m/7200....... We studied a frozen marine clay deposit at +35 m with stratified ice layers under sandy gravel top layer. During laboratory analysis using fall cone testing a thawed clay sample was found to be quick (St>700) due to dilution of pore water salts. Multidisciplinary approach was necessary for this study....

Electron transfer and atom exchange between aqueous Fe(II) and structural Fe(III) in clays. Role in U and Hg(II) transformations

Energy Technology Data Exchange (ETDEWEB)

Scherer, Michelle [Univ. of Iowa, Iowa City, IA (United States)

2016-08-31

During this project, we investigated Fe electron transfer and atom exchange between aqueous Fe(II) and structural Fe(III) in clay minerals. We used selective chemical extractions, enriched Fe isotope tracer experiments, computational molecular modeling, and Mössbauer spectroscopy. Our findings indicate that structural Fe(III) in clay minerals is reduced by aqueous Fe(II) and that electron transfer occurs when Fe(II) is sorbed to either basal planes and edge OH-groups of clay mineral. Findings from highly enriched isotope experiments suggest that up to 30 % of the Fe atoms in the structure of some clay minerals exhanges with aqueous Fe(II). First principles calculations using a small polaron hopping approach suggest surprisingly fast electron mobility at room temperature in a nontronite clay mineral and are consistent with temperature dependent Mössbauer data Fast electron mobility suggests that electrons may be able to conduct through the mineral fast enough to enable exchange of Fe between the aqueous phase and clay mineral structure. over the time periods we observed. Our findings suggest that Fe in clay minerals is not as stable as previously thought.

Contact angles at the water-air interface of hydrocarbon-contaminated soils and clay minerals

Science.gov (United States)

Sofinskaya, O. A.; Kosterin, A. V.; Kosterina, E. A.

2016-12-01

Contact angles at the water-air interface have been measured for triturated preparations of clays and soils in order to assess changes in their hydrophobic properties under the effect of oil hydrocarbons. Tasks have been to determine the dynamics of contact angle under soil wetting conditions and to reveal the effect of chemical removal of organic matter from soils on the hydrophilicity of preparations. The potentialities of static and dynamic drop tests for assessing the hydrophilic-hydrophobic properties of soils have been estimated. Clays (kaolinite, gumbrine, and argillite) have been investigated, as well as plow horizons of soils from the Republic of Tatarstan: heavy loamy leached chernozem, medium loamy dark gray forest soil, and light loamy soddy-calcareous soil. The soils have been contaminated with raw oil and kerosene at rates of 0.1-3 wt %. In the uncontaminated and contaminated chernozem, capillary water capacity has been maintained for 250 days. The contact angles have been found to depend on the degree of dispersion of powdered preparation, the main type of clay minerals in the soil, the presence and amount of oxidation-resistant soil organic matter, and the soil-water contact time. Characteristic parameters of mathematical models for drop behavior on triturated preparations have been calculated. Contamination with hydrocarbons has resulted in a reliable increase in the contact angles of soil preparations. The hydrophobization of soil surface in chernozem is more active than in soils poorer in organic matter. The complete restoration of the hydrophilic properties of soils after hydrocarbon contamination is due to the oxidation of easily oxidizable organic matter at the low content of humus, or to wetting during several months in the absence of the mazut fraction.

Electron Transfer Strategies Regulate Carbonate Mineral and Micropore Formation

Science.gov (United States)

Zeng, Zhirui; Tice, Michael M.

2018-01-01

Some microbial carbonates are robust biosignatures due to their distinct morphologies and compositions. However, whether carbonates induced by microbial iron reduction have such features is unknown. Iron-reducing bacteria use various strategies to transfer electrons to iron oxide minerals (e.g., membrane-bound enzymes, soluble electron shuttles, nanowires, as well as different mechanisms for moving over or attaching to mineral surfaces). This diversity has the potential to create mineral biosignatures through manipulating the microenvironments in which carbonate precipitation occurs. We used Shewanella oneidensis MR-1, Geothrix fermentans, and Geobacter metallireducens GS-15, representing three different strategies, to reduce solid ferric hydroxide in order to evaluate their influence on carbonate and micropore formation (micro-size porosity in mineral rocks). Our results indicate that electron transfer strategies determined the morphology (rhombohedral, spherical, or long-chained) of precipitated calcium-rich siderite by controlling the level of carbonate saturation and the location of carbonate formation. Remarkably, electron transfer strategies also produced distinctive cell-shaped micropores in both carbonate and hydroxide minerals, thus producing suites of features that could potentially serve as biosignatures recording information about the sizes, shapes, and physiologies of iron-reducing organisms.

222Rn and CO2 soil-gas geochemical characterization of thermally altered clays at Orciatico (Tuscany, Central Italy)

International Nuclear Information System (INIS)

Voltattorni, N.; Lombardi, S.; Rizzo, S.

2010-01-01

Research highlights: → Soil-gas technique is applied to study gas permeability of Orciatico clay units. → Clay permeability depends on thermal and mechanical alteration degree. → Soil-gas distributions are due to shallow fracturing of clays. → Rn and CO 2 soil-gas anomalies highlight secondary permeability in clay sequence. → Soil-gas results are supported by detailed geoelectrical surveys. - Abstract: The physical properties of clay allow argillaceous formations to be considered geological barriers to radionuclide migration in high-level radioactive-waste isolation systems. As laboratory simulations are short term and numerical models always involve assumptions and simplifications of the natural system, natural analogues are extremely attractive surrogates for the study of long-term isolation. The clays of the Orciatico area (Tuscany, Central Italy), which were thermally altered via the intrusion of an alkali-trachyte laccolith, represent an interesting natural model of a heat source which acted on argillaceous materials. The study of this natural analogue was performed through detailed geoelectrical and soil-gas surveys to define both the geometry of the intrusive body and the gas permeability of a clay unit characterized by different degrees of thermal alteration. The results of this study show that gas permeability is increased in the clay sequences subjected to greater heat input from the emplacement of the Orciatico intrusion, despite the lack of apparent mineral and geotechnical variations. These results, which take into consideration long time periods in a natural, large-scale geological system, may have important implications for the long-term safety of underground storage of nuclear waste in clay formations.

Use of bore logging for the determination of lithological characteristics of the Boom clay formation and interest for correlations in clay

International Nuclear Information System (INIS)

Neerdael, B.; Bonne, A.; Manfroy, P.; Vandenberghe, N.; Fierens, E.; Laga, P.

1981-01-01

It is first recalled that the purpose of the HADES project of the CEN/SCK at Mol (Belgium) is to study the possibility of geological disposal for radioactive wastes in the Boom clay formation at a depth between +-160 and 270 m. The different steps and aspects of the site investigation are exposed, and for each of them, the specific techniques used are reviewed. One of these steps is elaborated more in detail. It covers namely the lateral extrapolation of the lithological variations as established from a very detailed analysis of the initial cored boring. Among the usefull methods, the most practical and refined results were obtained from the resistivity logs in the reconnaissance holes. Finally, examples are shown of very detailed correlation on site scale, scale of the hydrogeological entity and regional scale (occurrence of Boom clay on the belgian territory)

Development of clay characterization methods for use in repository design with application to a natural Ca bentonite clay containing a redox front

International Nuclear Information System (INIS)

Karnland, O.; Pusch, R.

1990-12-01

Natural smectite clays in the form of 'true' bentonites formed from volcanic ash, or resulting from in-situ weathering of rock, are suitable for a number of sealing options in repositories, both as tightening component of sand/clay backfills and as highly efficient buffer for embedment of canisters, as well as for fracture sealing. The price and quality, in terms of smectite content and type of smectite, vary considerably and an optimum choice of clay for use in repositories has to be based on quantitative quality data. This requires characterization of the clay material for which a test scheme has been worked out. It comprises determination of the granulometrical, chemical, and mineralogical compositions, as well as of certain physical properties. Recent research shows the importance of the type of smectite for the longevity of buffers in repository environment, beidellite being less favourable and saponite superior to montmorillonite, which is the most common smectite species. The test scheme hence includes means of distinguishing between various smectite minerals. The influence of accessory minerals on the chemical integrity of both the smectite and the canister material requires identification also of such minerals, for which the scheme is useful as well. The report summarizes the various test procedures and gives data from application of the scheme to samples from a natural Ca bentonite containing a redox front. This study suggests that a significant part of the iron in the clay fraction is in the form of Fe 2+ in octahedral positions of the montmorillonite of unoxidized natural clay and that it is converted to Fe 3+ on oxidation. Part of the iron is probably in the form of the Fe 2+ Fe 3+ hydroxy compounds that give the unoxidized clay its bluish colour, while they can be assumed to be transformed to yellowish FeOOH forms on oxidation. (author)