Modeling coupled thermal, flow, transport and geochemical processes controlling near field long-term evolution

International Nuclear Information System (INIS)

Zhou, W.; Arthur, R.; Xu, T.; Pruess, K.

2005-01-01

Full text of publication follows: Bentonite is planned for use as a buffer material in the Swedish nuclear waste disposal concept (KBS-3). Upon emplacement, the buffer is expected to experience a complex set of coupled processes involving heating, re-saturation, reaction and transport of groundwater imbibed from the host rock. The effect of these processes may eventually lead to changes in desirable physical and rheological properties of the buffer, but these processes are not well understood. In this paper, a new quantitative model is evaluated to help improve our understanding of the long-term performance of buffer materials. This is an extension of a previous study [1] that involved simple thermal and chemical models applied to a fully saturated buffer. The thermal model in the present study uses heating histories for spent fuel in a single waste package [2]. The model uses repository dimensions, such as borehole and tunnel spacings [2], which affect the temperature distribution around the waste package. At the time of emplacement, bentonite is partially saturated with water having a different composition than the host-rock groundwater. The present model simulates water imbibition from the host rock into the bentonite under capillary and hydraulic pressure gradients. The associated chemical reactions and solute transport are simulated using Aespoe water composition [3]. The initial mineralogy of bentonite is assumed to be dominated by Na-smectite with much smaller amounts of anhydrite and calcite. Na-smectite dissolution is assumed to be kinetically-controlled while all other reactions are assumed to be at equilibrium controlled. All equilibrium and kinetic constants are temperature dependent. The modeling tool used is TOUGHREACT, developed by Lawrence Berkeley National Laboratory [4]. TOUGHREACT is a numerical model that is well suited for near-field simulations because it accounts for feedback between porosity and permeability changes from mineral

Significance of geochemical characterization to performance at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Simmons, A.M.

1993-01-01

The U.S. concept for permanent disposal of high-level radioactive waste resembles those of other countries in that it relies upon burial in a deep geologic medium. This concept relies upon multiple barriers to retard transport of radionuclides to the accessible environment; those barriers consist of the waste form, waste container, engineered barrier system (including possible backfill) and retardant properties of the host rock. Because mobilization of radionuclides is fundamentally a geochemical problem, an understanding of past, present, and future geochemical processes is a requisite part of site characterization studies conducted by the U.S. Department of Energy at Yucca Mountain, Nevada. Geochemical information is needed for evaluating three favorable conditions (the rates of geochemical processes, conditions that promote precipitation or sorption of radionuclides or prohibit formation of colloids, and stable mineral assemblages) and four potentially adverse conditions of the site (groundwater conditions that could increase the chemical reactivity of the engineered barried system or reduce sorption, potential for gaseous radionuclide movement, and oxidizing groundwaters) for key issues of radionuclide release, groundwater quality, and stability of the geochemical environment. Preliminary results of long-term heating experiments indicate that although zeolites can be modified by long-term, low temperature reactions, their beneficial sorptive properties will not be adversely affected. Mineral reactions will be controlled by the aqueous activity of silica in groundwater with which the minerals are in contact. Geochemical barriers alone may satisfy release requirements to the accessible environment for many radionuclides; however, additional site specific geochemical and mineralogical data are needed to test existing and future radionuclide transport models

Arsenic in groundwater of the Red River floodplain, Vietnam: Controlling geochemical processes and reactive transport modeling

DEFF Research Database (Denmark)

Postma, Diederik Jan; Larsen, Flemming; Hue, N.T.M.

2007-01-01

The mobilization of arsenic (As) to the groundwater was studied in a shallow Holocene aquifer on the Red River flood plain near Hanoi, Vietnam. The groundwater chemistry was investigated in a transect of 100 piezometers. Results show an anoxic aquifer featuring organic carbon decomposition......(III) but some As(V) is always found. Arsenic correlates well with NH4, relating its release to organic matter decomposition and the source of As appears to be the Fe-oxides being reduced. Part of the produced Fe(II) is apparently reprecipitated as siderite containing less As. Results from sediment extraction...... chemistry over depth is homogeneous and a reactive transport model was constructed to quantify the geochemical processes along the vertical groundwater flow component. A redox zonation model was constructed using the partial equilibrium approach with organic carbon degradation in the sediment as the only...

Geochemical and hydrodynamic phosphorus retention mechanisms in lowland catchments

NARCIS (Netherlands)

van der Grift, B.

2017-01-01

The release of phosphorus (P) to surface water from heavily fertilised agricultural fields is of major importance for surface water quality. The research reported in this thesis examined the role of geochemical and hydrodynamic processes controlling P speciation and transport in lowland catchments

Geochemical processes at a fresh/seawater interface in a shallow sandy aquifer

DEFF Research Database (Denmark)

Andersen, Martin Søgaard; Iversen, Vibeke Margrethe Nyvang; Postma, Diederik Jan

2001-01-01

Chemical processes in a natural fresh-/seawater mixing zone were studied in a shallow sandy aquifer. The dominant redox-processes are sulfate reduction and methanogenesis. Methanogenesis produces CO2, which causes calcite dissolution. The produced calcium induces ion exchange with sodium. The fin...... result of these interactions between different types of geochemical processes is an anoxic groundwater enriched in bicarbonate and sodium.......Chemical processes in a natural fresh-/seawater mixing zone were studied in a shallow sandy aquifer. The dominant redox-processes are sulfate reduction and methanogenesis. Methanogenesis produces CO2, which causes calcite dissolution. The produced calcium induces ion exchange with sodium. The final...

GEOCHEMICAL CONTROLS ON NUCLEAR MAGNETIC RESONANCE MEASUREMENTS

International Nuclear Information System (INIS)

Knight, Rosemary

2008-01-01

Proton nuclear magnetic resonance (NMR) is used in the Earth Sciences as a means of obtaining information about the molecular-scale environment of fluids in porous geological materials. Laboratory experiments were conducted to advance our fundamental understanding of the link between the NMR response and the geochemical properties of geological materials. In the first part of this research project, we studied the impact of both the surface-area-to-volume ratio (S/V) of the pore space and the surface relaxivity on the NMR response of fluids in sand-clay mixtures. This study highlighted the way in which these two parameters control our ability to use NMR measurements to detect and quantify fluid saturation in multiphase saturated systems. The second part of the project was designed to explore the way in which the mineralogic form of iron, as opposed to simply the concentration of iron, affects the surface relaxation rate and, more generally, the NMR response of porous materials. We found that the magnitude of the surface relaxation rate was different for the various iron-oxide minerals because of changes in both the surface-area-to-volume ratio of the pore space, and the surface relaxivity. Of particular significance from this study was the finding of an anomalously large surface relaxivity of magnetite compared to that of the other iron minerals. Differences in the NMR response of iron minerals were seen in column experiments during the reaction of ferrihydrite-coated quartz sand with aqueous Fe(II) solutions to form goethite, lepidocrocite and magnetite; indicating the potential use of NMR as a means of monitoring geochemical reactions. The final part of the research project investigated the impact of heterogeneity, at the pore-scale, on the NMR response. This work highlighted the way in which the geochemistry, by controlling the surface relaxivity, has a significant impact on the link between NMR data and the microgeometry of the pore space.

Geochemical Processes During Managed Aquifer Recharge With Desalinated Seawater

Science.gov (United States)

Ganot, Y.; Holtzman, R.; Weisbrod, N.; Russak, A.; Katz, Y.; Kurtzman, D.

2018-02-01

We study geochemical processes along the variably-saturated zone during managed aquifer recharge (MAR) with reverse-osmosis desalinated seawater (DSW). The DSW, post-treated at the desalination plant by calcite dissolution (remineralization) to meet the Israeli water quality standards, is recharged into the Israeli Coastal Aquifer through an infiltration pond. Water quality monitoring during two MAR events using suction cups and wells inside the pond indicates that cation exchange is the dominant subsurface reaction, driven by the high Ca2+ concentration in the post-treated DSW. Stable isotope analysis shows that the shallow groundwater composition is similar to the recharged DSW, except for enrichment of Mg2+, Na+, Ca2+, and HCO3-. A calibrated variably-saturated reactive transport model is used to predict the geochemical evolution during 50 years of MAR for two water quality scenarios: (i) post-treated DSW (current practice) and (ii) soft DSW (lacking the remineralization post-treatment process). The latter scenario was aimed to test soil-aquifer-treatment (SAT) as an alternative post-treatment technique. Both scenarios provide an enrichment of ˜2.5 mg L-1 in Mg2+ due to cation exchange, compared to practically zero Mg2+ currently found in the Israeli DSW. Simulations of the alternative SAT scenario provide Ca2+ and HCO3- remineralization due to calcite dissolution at levels that meet the Israeli standard for DSW. The simulated calcite content reduction in the sediments below the infiltration pond after 50 years of MAR was low (<1%). Our findings suggest that remineralization using SAT for DSW is a potentially sustainable practice at MAR sites overlying calcareous sandy aquifers.

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)

Identification of the Hydrogeochemical Processes in Groundwater Using Classic Integrated Geochemical Methods and Geostatistical Techniques, in Amol-Babol Plain, Iran

Science.gov (United States)

Sheikhy Narany, Tahoora; Ramli, Mohammad Firuz; Aris, Ahmad Zaharin; Sulaiman, Wan Nor Azmin; Juahir, Hafizan; Fakharian, Kazem

2014-01-01

Hydrogeochemical investigations had been carried out at the Amol-Babol Plain in the north of Iran. Geochemical processes and factors controlling the groundwater chemistry are identified based on the combination of classic geochemical methods with geographic information system (GIS) and geostatistical techniques. The results of the ionic ratios and Gibbs plots show that water rock interaction mechanisms, followed by cation exchange, and dissolution of carbonate and silicate minerals have influenced the groundwater chemistry in the study area. The hydrogeochemical characteristics of groundwater show a shift from low mineralized Ca-HCO3, Ca-Na-HCO3, and Ca-Cl water types to high mineralized Na-Cl water type. Three classes, namely, C1, C2, and C3, have been classified using cluster analysis. The spatial distribution maps of Na+/Cl−, Mg2+/Ca2+, and Cl−/HCO3 − ratios and electrical conductivity values indicate that the carbonate and weathering of silicate minerals played a significant role in the groundwater chemistry on the southern and western sides of the plain. However, salinization process had increased due to the influence of the evaporation-precipitation process towards the north-eastern side of the study area. PMID:24523640

Actual stage of organic geochemical knowledge from Campos and Espirito Santo basins, Brazil

International Nuclear Information System (INIS)

Gaglianone, P.C.; Trindade, L.A.F.

1987-01-01

Campos and Espirito Santo basins display several similar geochemical aspects. The microbial and other degradation processes caused changes in the composition of the oils in the reservoir rocks. The oils are biodegraded in different degrees, with the reservoir temperature developing an important role in the control of the biodegradation process. The migration pathway model is similar for Campos and Espirito Santo basins, involving the upward secondary migration through a window in the evaporitic seals. The oils passed to the marine sequence where migration and accumulation were controlled by faults, regional unconformities and by reservoirs. The geochemical correlation of oils are realized by gaseous and liquid chromatography analysis, carbon isotopes and biolabelled compounds. (author)

Geochemical modelling baseline compositions of groundwater

DEFF Research Database (Denmark)

Postma, Diederik Jan; Kjøller, Claus; Andersen, Martin Søgaard

2008-01-01

and variations in water chemistry that are caused by large scale geochemical processes taking place at the timescale of thousands of years. The most important geochemical processes are ion exchange (Valreas and Aveiro) where freshwater solutes are displacing marine ions from the sediment surface, and carbonate......Reactive transport models, were developed to explore the evolution in groundwater chemistry along the flow path in three aquifers; the Triassic East Midland aquifer (UK), the Miocene aquifer at Valreas (F) and the Cretaceous aquifer near Aveiro (P). All three aquifers contain very old groundwaters...... dissolution (East Midlands, Valreas and Aveiro). Reactive transport models, employing the code PHREEQC, which included these geochemical processes and one-dimensional solute transport were able to duplicate the observed patterns in water quality. These models may provide a quantitative understanding...

Geochemical evolution of groundwater in the Mud Lake area, eastern Idaho, USA

Science.gov (United States)

Rattray, Gordon W.

2015-01-01

Groundwater with elevated dissolved-solids concentrations—containing large concentrations of chloride, sodium, sulfate, and calcium—is present in the Mud Lake area of Eastern Idaho. The source of these solutes is unknown; however, an understanding of the geochemical sources and processes controlling their presence in groundwater in the Mud Lake area is needed to better understand the geochemical sources and processes controlling the water quality of groundwater at the Idaho National Laboratory. The geochemical sources and processes controlling the water quality of groundwater in the Mud Lake area were determined by investigating the geology, hydrology, land use, and groundwater geochemistry in the Mud Lake area, proposing sources for solutes, and testing the proposed sources through geochemical modeling with PHREEQC. Modeling indicated that sources of water to the eastern Snake River Plain aquifer were groundwater from the Beaverhead Mountains and the Camas Creek drainage basin; surface water from Medicine Lodge and Camas Creeks, Mud Lake, and irrigation water; and upward flow of geothermal water from beneath the aquifer. Mixing of groundwater with surface water or other groundwater occurred throughout the aquifer. Carbonate reactions, silicate weathering, and dissolution of evaporite minerals and fertilizer explain most of the changes in chemistry in the aquifer. Redox reactions, cation exchange, and evaporation were locally important. The source of large concentrations of chloride, sodium, sulfate, and calcium was evaporite deposits in the unsaturated zone associated with Pleistocene Lake Terreton. Large amounts of chloride, sodium, sulfate, and calcium are added to groundwater from irrigation water infiltrating through lake bed sediments containing evaporite deposits and the resultant dissolution of gypsum, halite, sylvite, and bischofite.

Rock–water interactions and pollution processes in the volcanic aquifer system of Guadalajara, Mexico, using inverse geochemical modeling

International Nuclear Information System (INIS)

Morán-Ramírez, J.; Ledesma-Ruiz, R.; Mahlknecht, J.; Ramos-Leal, J.A.

2016-01-01

In order to understand and mitigate the deterioration of water quality in the aquifer system underlying Guadalajara metropolitan area, an investigation was performed developing geochemical evolution models for assessment of groundwater chemical processes. The models helped not only to conceptualize the groundwater geochemistry, but also to evaluate the relative influence of anthropogenic inputs and natural sources of salinity to the groundwater. Mixing processes, ion exchange, water–rock–water interactions and nitrate pollution and denitrification were identified and confirmed using mass-balance models constraint by information on hydrogeology, groundwater chemistry, lithology and stability of geochemical phases. The water–rock interactions in the volcanic setting produced a dominant Na−HCO_3 water type, followed by Na−Mg−Ca−HCO_3 and Na−Ca−HCO_3. For geochemical evolution modeling, flow sections were selected representing recharge and non-recharge processes and a variety of mixing conditions. Recharge processes are dominated by dissolution of soil CO_2 gas, calcite, gypsum, albite and biotite, and Ca/Na exchange. Non-recharge processes show that the production of carbonic acid and Ca/Na exchange are decreasing, while other minerals such as halite and amorphous SiO_2 are precipitated. The origin of nitrate pollution in groundwater are fertilizers in rural plots and wastewater and waste disposal in the urban area. This investigation may help water authorities to adequately address and manage groundwater contamination. - Highlights: • The Inverse geochemical modeling was used to study to processes occurring in a volcanic aquifer. • Three flow sections were selected to apply inverse hydrogeochemical modeling. • Three main groundwater flows were identified: a local, intermediate and regional flow. • The models show that in the study area that groundwater is mixed with local recharge. • In the south, the aquifer has thermal influence.

Geochemical Constraints for Mercury's PCA-Derived Geochemical Terranes

Science.gov (United States)

Stockstill-Cahill, K. R.; Peplowski, P. N.

2018-05-01

PCA-derived geochemical terranes provide a robust, analytical means of defining these terranes using strictly geochemical inputs. Using the end members derived in this way, we are able to assess the geochemical implications for Mercury.

The effects of sorting by aeolian processes on the geochemical characteristics of surface materials: a wind tunnel experiment

Science.gov (United States)

Wang, Xunming; Lang, Lili; Hua, Ting; Zhang, Caixia; Li, Hui

2018-03-01

The geochemical characteristics of aeolian and surface materials in potential source areas of dust are frequently employed in environmental reconstructions as proxies of past climate and as source tracers of aeolian sediments deposited in downwind areas. However, variations in the geochemical characteristics of these aeolian deposits that result from near-surface winds are currently poorly understood. In this study, we collected surface samples from the Ala Shan Plateau (a major potential dust source area in Central Asia) to determine the influence of aeolian processes on the geochemical characteristics of aeolian transported materials. Correlation analyses show that compared with surface materials, the elements in transported materials (e.g., Cu, As, Pb, Mn, Zn, Al, Ca, Fe, Ga, K, Mg, P, Rb, Co, Cr, Na, Nb, Si, and Zr) were subjected to significant sorting by aeolian processes, and the sorting also varied among different particle size fractions and elements. Variations in wind velocity were significantly correlated with the contents of Cr, Ga, Sr, Ca, Y, Nd, Zr, Nb, Ba, and Al, and with the Zr/Al, Zr/Rb, K/Ca, Sr/Ca, Rb/Sr, and Ca/Al ratios. Given the great variation in the geochemical characteristics of materials transported under different aeolian processes relative to those of the source materials, these results indicate that considerable uncertainty may be introduced to analyses by using surface materials to trace the potential source areas of aeolian deposits that accumulate in downwind areas.

Geochemical differentiation processes for arc magma of the Sengan volcanic cluster, Northeastern Japan, constrained from principal component analysis

Science.gov (United States)

Ueki, Kenta; Iwamori, Hikaru

2017-10-01

In this study, with a view of understanding the structure of high-dimensional geochemical data and discussing the chemical processes at work in the evolution of arc magmas, we employed principal component analysis (PCA) to evaluate the compositional variations of volcanic rocks from the Sengan volcanic cluster of the Northeastern Japan Arc. We analyzed the trace element compositions of various arc volcanic rocks, sampled from 17 different volcanoes in a volcanic cluster. The PCA results demonstrated that the first three principal components accounted for 86% of the geochemical variation in the magma of the Sengan region. Based on the relationships between the principal components and the major elements, the mass-balance relationships with respect to the contributions of minerals, the composition of plagioclase phenocrysts, geothermal gradient, and seismic velocity structure in the crust, the first, the second, and the third principal components appear to represent magma mixing, crystallizations of olivine/pyroxene, and crystallizations of plagioclase, respectively. These represented 59%, 20%, and 6%, respectively, of the variance in the entire compositional range, indicating that magma mixing accounted for the largest variance in the geochemical variation of the arc magma. Our result indicated that crustal processes dominate the geochemical variation of magma in the Sengan volcanic cluster.

Geochemical and isotopic study to determine sources and processes affecting nitrate and sulphate in groundwater influenced by intensive human activity - carbonate aquifer Gliwice (southern Poland)

International Nuclear Information System (INIS)

Jakóbczyk-Karpierz, Sabina; Sitek, Sławomir; Jakobsen, Rasmus; Kowalczyk, Andrzej

2017-01-01

A multi-species, multi-stable-isotope approach (δ"1"5N_N_O_3, δ"1"8O_N_O_3_, δ"3"4S_S_O_4, δ"1"8O_S_O_4, δ"1"8O_H_2_O and δ"2H_H_2_O) was used together with environmental tracers (Ar, Ne, CFC-11 and CFC-12) and geochemical modelling to characterize sources and processes controlling concentrations of NO_3"− and SO_4"2"- in groundwater of the carbonate aquifer Gliwice (southern Poland). The study area represents a strongly transformed environment with a range of human activities i.a. Agriculture, urbanization and industry. The δ"1"5N_N_O_3 and δ"1"8O_N_O_3 indicated that most samples contained NO_3"− of mixed sources: artificial fertilizers, municipal and industrial sewage, while very good correlation between NO_3"− and CFC-12 suggested that nitrate originated primarily from residential and industrial sewage. Conversely, isotopic composition of sulphate in groundwater suggested agriculture as well as oxidation of sulphides as dominant. The conclusion was supported by the comparison of CFCs and sulphate concentrations which revealed no relevant correlation. Geochemical modelling confirmed the presence of sulphate reduction in areas where isotopic analyses were not possible due to undetectable sulphate. Thus, the integrated application of stable isotopes, environmental tracers, groundwater chemistry and geochemical modelling shows a complex origin of groundwater pollution in the study area as well as variety of geochemical processes controlling chemistry of groundwater in a triple-porosity aquifer influenced by different types of human activity. - Highlights: • CFCs helped to identify municipal and industrial sources of NO_3"− in groundwater. • δ"1"8O and δ"3"4S suggested domination of SO_4"2"- from agriculture and sulphide oxidation. • Sulphate reduction was confirmed using geochemical modelling for SO_4"2"-free water.

Coastal Aquifer Contamination and Geochemical Processes Evaluation in Tugela Catchment, South Africa—Geochemical and Statistical Approaches

Directory of Open Access Journals (Sweden)

Badana Ntanganedzeni

2018-05-01

Full Text Available Assessment of groundwater quality, contamination sources and geochemical processes in the coastal aquifer of Tugela Catchment, South Africa were carried out by the geochemical and statistical approach using major ion chemistry of 36 groundwater samples. Results suggest that the spatial distribution pattern of EC, TDS, Na, Mg, Cl and SO4 are homogenous and elevated concentrations are observed in the wells in the coastal region and few wells near the Tugela River. Wells located far from the coast are enriched by Ca, HCO3 and CO3. Durov diagrams, Gibbs plots, ionic ratios, chloro alkaline indices (CAI1 and CAI2 and correlation analysis imply that groundwater chemistry in the coastal aquifer of Tugela Catchment is regulated by the ion exchange, mineral dissolution, saline sources, and wastewater infiltration from domestic sewage; septic tank leakage and irrigation return flow. Principle component analysis also ensured the role of saline and anthropogenic sources and carbonates dissolution on water chemistry. Spatial distributions of factor score also justify the above predictions. Groundwater suitability assessment indicates that around 80% and 90% of wells exceeded the drinking water standards recommended by the WHO and South African drinking water standards (SAWQG, respectively. Based on SAR, RSC, PI, and MH classifications, most of the wells are suitable for irrigation in the study region. USSL classification suggests that groundwater is suitable for coarse-textured soils and salt-tolerant crops. The study recommends that a proper management plan is required to protect this coastal aquifer efficiently.

Modeling of geochemical processes in the submarine discharge zone of hydrothermal solutions

Directory of Open Access Journals (Sweden)

С. М. Судариков

2017-06-01

Full Text Available The paper reviews the main methods and analyzes modeling results for geochemical processes in the submarine discharge zone of hydrothermal solutions of mid-ocean ridges. Initial data for modeling have been obtained during several marine expeditions, including Russian-French expedition SERPENTINE on the research vessel «Pourquoi Рas?» (2007. Results of field observations, laboratory experiments and theoretical developments are supported by the analysis of regression model of mixing between hydrothermal solutions and sea water. Verification of the model has been carried out and the quality of chemical analysis has been assessed; degree and character of participation of solution components in the hydrothermal process have been defined; the content of end members has been calculated basing on reverse forecasting of element concentration, depending on regression character; data for thermodynamic modeling have been prepared. Regression model of acid-base properties and chloridity of mineralizing thermal springs confirms adequacy of the model of double-diffusive convection for forming the composition of hydrothermal solutions.  Differentiation of solutions according to concentrations of chloride-ion, depending on temperature and pH indicator within this model, is associated with phase conversions and mixing of fluids from two convection cells, one of which is a zone of brine circulation. In order to carry out computer thermodynamic modeling, hydro-geochemical and physicochemical models of hydrothermal discharge zone have been created. Verification of the model has been carried out basing on changes of Mn concentration in the hydrothermal plume. Prevailing forms of Mn migration in the plume are Mn2+, MnCl+, MnCl2. Two zones have been identified in the geochemical structure of the plume: 1 high-temperature zone (350-100 °С with prevalence of chloride complexes – ascending plume; 2 low-temperature zone (100-2 °С, where predominant form of

Linking geochemical processes in mud volcanoes with arsenic mobilization driven by organic matter.

Science.gov (United States)

Liu, Chia-Chuan; Kar, Sandeep; Jean, Jiin-Shuh; Wang, Chung-Ho; Lee, Yao-Chang; Sracek, Ondra; Li, Zhaohui; Bundschuh, Jochen; Yang, Huai-Jen; Chen, Chien-Yen

2013-11-15

The present study deals with geochemical characterization of mud fluids and sediments collected from Kunshuiping (KSP), Liyushan (LYS), Wushanting (WST), Sinyangnyuhu (SYNH), Hsiaokunshui (HKS) and Yenshuikeng (YSK) mud volcanoes in southwestern Taiwan. Chemical constituents (cations, anions, trace elements, organic carbon, humic acid, and stable isotopes) in both fluids and mud were analyzed to investigate the geochemical processes and spatial variability among the mud volcanoes under consideration. Analytical results suggested that the anoxic mud volcanic fluids are highly saline, implying connate water as the probable source. The isotopic signature indicated that δ(18)O-rich fluids may be associated with silicate and carbonate mineral released through water-rock interaction, along with dehydration of clay minerals. Considerable amounts of arsenic in mud irrespective of fluid composition suggested possible release through biogeochemical processes in the subsurface environment. Sequential extraction of As from the mud indicated that As was mostly present in organic and sulphidic phases, and adsorbed on amorphous Mn oxyhydroxides. Volcanic mud and fluids are rich in organic matter (in terms of organic carbon), and the presence of humic acid in mud has implications for the binding of arsenic. Functional groups of humic acid also showed variable sources of organic matter among the mud volcanoes being examined. Because arsenate concentration in the mud fluids was found to be independent from geochemical factors, it was considered that organic matter may induce arsenic mobilization through an adsorption/desorption mechanism with humic substances under reducing conditions. Organic matter therefore plays a significant role in the mobility of arsenic in mud volcanoes. Copyright © 2012 Elsevier B.V. All rights reserved.

Appliance of geochemical engineering in radioactive waste disposal

International Nuclear Information System (INIS)

Li Shuang; Zhang Chengjiang; Ni Shijun; Li Kuanliang

2008-01-01

The basic foundation of applying geochemical engineering to control environment, common engineering models of disposal radioactive waste and the functions of the engineering barriers are introduced in this paper. The authors take the geochemical engineering barrier materiel research of a radioactive waste repository as an example to explain the appliance of geochemical engineering in the disposal of radioactive waste. And the results show that it can enhance the security of the nuclear waste repository if we use geochemical engineering barrier. (authors)

Linking geochemical processes in mud volcanoes with arsenic mobilization driven by organic matter

Energy Technology Data Exchange (ETDEWEB)

Liu, Chia-Chuan; Kar, Sandeep [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Jean, Jiin-Shuh, E-mail: jiinshuh@mail.ncku.edu.tw [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Wang, Chung-Ho [Institute of Earth Sciences, Academia Sinica, Taipei, Taiwan (China); Lee, Yao-Chang [National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan (China); Sracek, Ondra [OPV s.r.o. (Groundwater Protection Ltd.), Bělohorská 31, 169 00 Praha 6 (Czech Republic); Department of Geology, Faculty of Science, Palacký University, 17. listopadu 12, 771 46 Olomouc (Czech Republic); Li, Zhaohui [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Department of Geosciences, University of Wisconsin – Parkside, Kenosha, WI 53144 (United States); Bundschuh, Jochen [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Faculty of Engineering and Surveying and National Centre for Engineering in Agriculture, The University of Southern Queensland, Toowoomba (Australia); Yang, Huai-Jen [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Chen, Chien-Yen [Department of Earth and Environmental Sciences, National Chung Cheng University, Chiayi 621, Taiwan (China)

2013-11-15

Highlights: ► Study represents geochemical characteristics and their spatial variability among six mud volcanoes of southern Taiwan. ► Anoxic mud volcanic fluids containing high NaCl imply connate water as the possible source. ► δ{sup 18}O-rich fluids is associated with silicate and carbonate mineral released through water–rock interaction. ► High As content in mud and its sequential extraction showed mostly adsorbed As on organic and sulphidic phases. ► Organic matter specially humic acid showed redox dependence and it may play an important role in binding and mobility of arsenic. -- Abstract: The present study deals with geochemical characterization of mud fluids and sediments collected from Kunshuiping (KSP), Liyushan (LYS), Wushanting (WST), Sinyangnyuhu (SYNH), Hsiaokunshui (HKS) and Yenshuikeng (YSK) mud volcanoes in southwestern Taiwan. Chemical constituents (cations, anions, trace elements, organic carbon, humic acid, and stable isotopes) in both fluids and mud were analyzed to investigate the geochemical processes and spatial variability among the mud volcanoes under consideration. Analytical results suggested that the anoxic mud volcanic fluids are highly saline, implying connate water as the probable source. The isotopic signature indicated that δ{sup 18}O-rich fluids may be associated with silicate and carbonate mineral released through water–rock interaction, along with dehydration of clay minerals. Considerable amounts of arsenic in mud irrespective of fluid composition suggested possible release through biogeochemical processes in the subsurface environment. Sequential extraction of As from the mud indicated that As was mostly present in organic and sulphidic phases, and adsorbed on amorphous Mn oxyhydroxides. Volcanic mud and fluids are rich in organic matter (in terms of organic carbon), and the presence of humic acid in mud has implications for the binding of arsenic. Functional groups of humic acid also showed variable sources of

Geochemical processes controlling minewater pollution

International Nuclear Information System (INIS)

Banks, D.

2004-01-01

Minewater is a subset of groundwater, subject to broadly similar hydrochemical processes. In 'normal' groundwaters, access to oxidizing species is poor and acid-base reactions tend to dominate over oxidation reactions. Acid-base reactions such as carbonate dissolution and silicate hydrolysis consume protons and carbon dioxide, and release alkalinity and base cations. In mines, the atmospheric environment is rapidly introduced to the deep reducing geosphere (or vice versa in the case of mine waste deposits). This carries the possibility of intense and rapid oxidation of sulphide minerals such as pyrite, to such an extent that these acid-generating redox reactions may dominate over acid-base 'neutralization' reactions and result in the phenomenon of 'acid rock drainage' (ARD). In ARD, a negative correlation is typically observed between pH and concentrations of many metals and metalloids, base cations and sulphate. This correlation is due to genetic co-variation - generation of protons, sulphate and metals in sulphide weathering reactions, pH-dependent solubility of many ARD-related metals and low pH intensifying carbonate dissolution and silicate hydrolysis to release aluminium, silica and base cations. This paper examines the reactions involved in ARD generation and neutralization, and attempts to clarify key concepts such as pH, Eh, alkalinity, acidity and equilibrium constants. Refs. 42 (author)

TAPIR--Finnish national geochemical baseline database.

Science.gov (United States)

Jarva, Jaana; Tarvainen, Timo; Reinikainen, Jussi; Eklund, Mikael

2010-09-15

In Finland, a Government Decree on the Assessment of Soil Contamination and Remediation Needs has generated a need for reliable and readily accessible data on geochemical baseline concentrations in Finnish soils. According to the Decree, baseline concentrations, referring both to the natural geological background concentrations and the diffuse anthropogenic input of substances, shall be taken into account in the soil contamination assessment process. This baseline information is provided in a national geochemical baseline database, TAPIR, that is publicly available via the Internet. Geochemical provinces with elevated baseline concentrations were delineated to provide regional geochemical baseline values. The nationwide geochemical datasets were used to divide Finland into geochemical provinces. Several metals (Co, Cr, Cu, Ni, V, and Zn) showed anomalous concentrations in seven regions that were defined as metal provinces. Arsenic did not follow a similar distribution to any other elements, and four arsenic provinces were separately determined. Nationwide geochemical datasets were not available for some other important elements such as Cd and Pb. Although these elements are included in the TAPIR system, their distribution does not necessarily follow the ones pre-defined for metal and arsenic provinces. Regional geochemical baseline values, presented as upper limit of geochemical variation within the region, can be used as trigger values to assess potential soil contamination. Baseline values have also been used to determine upper and lower guideline values that must be taken into account as a tool in basic risk assessment. If regional geochemical baseline values are available, the national guideline values prescribed in the Decree based on ecological risks can be modified accordingly. The national geochemical baseline database provides scientifically sound, easily accessible and generally accepted information on the baseline values, and it can be used in various

Alaska Geochemical Database (AGDB)-Geochemical data for rock, sediment, soil, mineral, and concentrate sample media

Science.gov (United States)

Granitto, Matthew; Bailey, Elizabeth A.; Schmidt, Jeanine M.; Shew, Nora B.; Gamble, Bruce M.; Labay, Keith A.

2011-01-01

The Alaska Geochemical Database (AGDB) was created and designed to compile and integrate geochemical data from Alaska in order to facilitate geologic mapping, petrologic studies, mineral resource assessments, definition of geochemical baseline values and statistics, environmental impact assessments, and studies in medical geology. This Microsoft Access database serves as a data archive in support of present and future Alaskan geologic and geochemical projects, and contains data tables describing historical and new quantitative and qualitative geochemical analyses. The analytical results were determined by 85 laboratory and field analytical methods on 264,095 rock, sediment, soil, mineral and heavy-mineral concentrate samples. Most samples were collected by U.S. Geological Survey (USGS) personnel and analyzed in USGS laboratories or, under contracts, in commercial analytical laboratories. These data represent analyses of samples collected as part of various USGS programs and projects from 1962 to 2009. In addition, mineralogical data from 18,138 nonmagnetic heavy mineral concentrate samples are included in this database. The AGDB includes historical geochemical data originally archived in the USGS Rock Analysis Storage System (RASS) database, used from the mid-1960s through the late 1980s and the USGS PLUTO database used from the mid-1970s through the mid-1990s. All of these data are currently maintained in the Oracle-based National Geochemical Database (NGDB). Retrievals from the NGDB were used to generate most of the AGDB data set. These data were checked for accuracy regarding sample location, sample media type, and analytical methods used. This arduous process of reviewing, verifying and, where necessary, editing all USGS geochemical data resulted in a significantly improved Alaska geochemical dataset. USGS data that were not previously in the NGDB because the data predate the earliest USGS geochemical databases, or were once excluded for programmatic reasons

Geochemical processes during managed aquifer recharge with desalinated seawater

Science.gov (United States)

Ganot, Y.; Holtzman, R.; Weisbrod, N.; Russak, A.; Katz, Y.; Kurtzman, D.

2017-12-01

In this work we study the geochemical processes along the variably-saturated zone during managed aquifer recharge (MAR) with reverse-osmosis desalinated seawater (DSW) to an infiltration pond at the Menashe site, located above the Israeli coastal aquifer. The DSW is post-treated by calcite dissolution (remineralization) in order to meet the Israeli desalinated water quality criteria. Suction cups and monitoring wells inside the pond were used to monitor water quality during two MAR events on 2015 and 2016. Results show that cation exchange is dominant, driven by the high Ca2+ concentration in the post-treated DSW. Stable isotope analysis shows that the composition of the shallow groundwater is similar to the recharged DSW, but with enrichment of Mg2+, Na+, Ca2+ and HCO3-. A calibrated variably-saturated reactive transport model was used to predict the geochemical evolution during 50 years of MAR with two water quality scenarios: post-treated DSW and soft DSW (without post-treatment). The latter scenario was aimed to test soil-aquifer-treatment as an alternative post-treatment technique. In terms of water quality, the results of the two scenarios were found within the range of the desalinated water criteria. Mg2+ enrichment was stable ( 2.5 mg L-1), higher than the zero concentration found in the Israeli DSW. Calcite content reduction was low (<1%) along the variably-saturated profile, after 50 years of MAR. This suggests that using soil-aquifer-treatment as a remineralization technique for DSW is potentially a sustainable practice, which is limited only by the current hydraulic capacity of the Menashe MAR site.

Methodological approaches in estimating anomalous geochemical field structure

International Nuclear Information System (INIS)

Gavrilov, R; Rudmin, M

2015-01-01

Mathematical statistic methods were applied to analyze the core samples from vertical expendable wells in Chertovo Koryto gold ore field. The following methods were used to analyse gold in samples: assay tests and atomic absorption method (AAS), while emission spectrum semiquantative method was applied to identify traces. The analysis of geochemical association distribution in one central profile demonstrated that bulk metasomatic aureoles are characteristic of concentric zonal structure. The distribution of geochemical associations is correlated to the hydrothermal stages of mineral formation identified in this deposit. It was proved that the processed geochemical data by factor and cluster analyses provided additional information on the anomalous geochemical field structure in gold- bearing black-shale strata. Such methods are effective tools in interpretating specific features of geochemical field structures in analogous potential ore-bearing areas

Alligator Rivers Analogue project. Geochemical Data Bases

International Nuclear Information System (INIS)

Bennett, D.G.; Read, D.

1992-01-01

The Koongarra uranium deposit in the Northern Territory of Australia is being studied to evaluate the processes involved in the geochemical alteration of the ore body and the formation of the uranium dispersion fan. A broad range of research is being undertaken into the geochemistry and hydrology of the site with the aim of understanding the transport of radionuclides through the system. During the project a range of geochemical and hydrogeochemical models have been developed to account for measured data from the site and with which to predict site evolution. The majority of these models are based on the premise of thermodynamic chemical equilibrium and employ fundamental thermodynamic data to characterise the chemistry of the system. From the differences which exist between the thermodynamic data bases (Appendices I and II) it is possible to gain a view of the level of uncertainty associated with thermodynamic data in each set of calculations. This report gives a brief introduction to the geochemical processes underlying the models, and details the equations used to quantify the more common of these processes (e.g. aqueous speciation and mineral solubility). A description is given of the computer codes (EQ3/6, PHREEQE, MINTEQ) most commonly used during the project for geochemical modelling. Their key features are highlighted and comparisons made. It is concluded that the degree of uncertainty in geochemical modelling studies arising as a result of using one code rather than another is relatively insignificant when compared to that related to differences in the underlying data bases. 73 refs., 3 figs

Geochemical study of water-rock interaction processes on geothermal systems of alkaline water in granitic massif

International Nuclear Information System (INIS)

Buil gutierrez, B.; Garcia Sanz, S.; Lago San Jose, M.; Arranz Yague, E.; Auque Sanz, L.

2002-01-01

The study of geothermal systems developed within granitic massifs (with alkaline waters and reducing ORP values) is a topic of increasing scientific interest. These systems are a perfect natural laboratory for studying the water-rock interaction processes as they are defined by three main features: 1) long residence time of water within the system, 2) temperature in the reservoir high enough to favour reaction kinetics and finally, 3) the comparison of the chemistry of the incoming and outgoing waters of the system allows for the evaluation of the processes that have modified the water chemistry and its signature, The four geothermal systems considered in this paper are developed within granitic massifs of the Spanish Central Pyrenes; these systems were studied from a geochemical point of view, defining the major, trace and REE chemistry of both waters and host rocks and then characterizing the composition and geochemical evolution of the different waters. Bicarbonate-chloride-sodic and bicarbonate-sodic compositions are the most representative of the water chemistry in the deep geothermal system, as they are not affected by secondary processes (mixing, conductive cooling, etc). (Author)

The identification of provenance-controlled facies by geochemical methods on a portion of the Vaal Reef, Klerksdorp Goldfield

International Nuclear Information System (INIS)

Henckel, J.; Schweitzer, J.K.; Horsch, H.

1990-01-01

The use of geochemical methods for identifying provenance controlled facies in Witwatersrand reefs is considered. Three methods - whole rock geochemistry, zircon analysis, and chromite analysis - have been evaluated in order to establish the feasibility of using these geochemical techniques. An area of Vaal Reef where two sedimentological facies with distinct gold distributions had previously been identified was investigated. The studies reported here gave evidence of differences in the source areas for these two facies. Accordingly, it is concluded that the application of geochemistry to identify provenance-controlled facies is a useful technique which can help geologists arrive at a better interpretation of depositional systems within Witwatersrand reefs and thereby assist in the understanding of gold distribution patterns. 26 refs., 11 figs., 4 tabs

Sharp fronts within geochemical transport problems

International Nuclear Information System (INIS)

Grindrod, P.

1995-01-01

The authors consider some reactive geochemical transport problems in groundwater systems. When incoming fluid is in disequilibrium with the mineralogy sharp transition fronts may develop. They show that this is a generic property for a class of systems where the timescales associated with reaction and diffusion phenomena are much shorter than those associated with advective transport. Such multiple timescale problems are relevant to a variety of processes in natural systems: mathematically methods of singular perturbation theory reduce the dimension of the problems to be solved locally. Furthermore, they consider how spatial heterogeneous mineralogy can impact upon the propagation of sharp geochemical fronts. The authors developed an asymptotic approach in which they solve equations for the evolving geometry of the front and indicate how the non-smooth perturbations due to natural heterogeneity of the mineralogy on underlying ground water flow field are balanced against the smoothing effect of diffusion/dispersive processes. Fronts are curvature damped, and the results here indicate the generic nature of separate front propagation within both model (idealized) and natural (heterogeneous) geochemical systems

Hydrochemical evaluation and identification of geochemical processes in the shallow and deep wells in the Ramganga Sub-Basin, India.

Science.gov (United States)

Rajmohan, Natarajan; Patel, Neelam; Singh, Gaurav; Amarasinghe, Upali A

2017-09-01

Groundwater samples were collected from 44 wells in the Ramganga Sub-Basin (RSB), India, and analysed for major ions, nutrients and trace metals. The primary goal of this study is to evaluate the hydrochemistry and to identify the geochemical processes that govern the water chemistry in the shallow and deep tube wells in the study area using geochemical methods. The knowledge of changes in hydrochemistry of the aquifers is important for both groundwater recharge and use in the region. This study found that there are substantial differences of water chemistry between shallow and deep wells. In the shallow wells, the average concentrations of total dissolved solid (TDS), Na, K, Ca, Mg, HCO 3 , Cl, SO 4 , NO 3 , PO 4 , F, Cu, Mn, Fe and Cr are twofold higher than the deep wells. The concentrations of dissolved silica in the groundwater do not vary with the depth, which implies that the variation in the water chemistry is not due to mineral dissolution alone. Major ion ratios and saturation indices suggest that the water chemistry is predominantly controlled by dissolution of carbonate minerals, silicate weathering and ion exchange reactions. Thermodynamic evaluation (ion activity ratios and stability filed diagrams) indicates that the kaolinite and gibbsite controlled the water chemistry in the both shallow and deep wells. In addition, the groundwater chemistry in the shallow wells is affected by the vertical infiltration of contaminated water from surface contamination sources and nitrification process. In the deep wells, absence of NO 3 and low concentrations of Cl, SO 4 , PO 4 and F imply the role of regional flow and denitrification in the groundwater. Results concluded that proper management plan is necessary to protect the shallow aquifer in the RSB since shallow aquifer pumping is less expensive than the deeper one.

Petrological mineralogical and geochemical characterization of the granitoids and fracture fillings developed in Ratones Mines (Spain)

International Nuclear Information System (INIS)

Buil Gutierrez, B.

2002-01-01

The petrological, mineralogical and geochemical characterisation of the granitoids and fracture fillings developed in the Ratones Mine (Caceres, Spain) has been done in order to understand rock-water interaction processes which control water geochemical parameters. Special interest has been devoted to the analysis and interpretation of REE patterns in the solid phase (granitoids and fracture fillings) because they constitute geochemical tracers in water-rock interaction process. Moreover, REE are considered as actinide analogues. In order to characterise the solid phase (granitoids and fracture fillings) several investigation scales (system, outcrop, whole rock, mineral and geochemical components) have been considered and different types of samples have been analysed. These factors control the methodological approach used in this investigation. The analytical methods we have used in this investigation are microscope, qualitative and semi-quantitative methods (XRD, SEM,EDAX) and quantitative methods (ICP-MS, XRF, EM, LAM-IC-MS). The bulk of the granitoids located around the Ratones Mine Belongs to the alkaline feldspar granite-sienogranite lihotype and they show a peraluminous and subalkaline pattern. From the mineralogical point of view, they are composed by quartz, K-feldspar (Or>90%), showing sericitation, moscovitization and turmolinization altherations, alkaline plagioclase (An-=-3%), usually altered to sericite, saussirite and less frequently affected by moscovitization processes, Fe-Al biotite, frequently affected by chloritization processes and sometimes replaced by muscovite, and finally muscovite (>2% celadonite and <4% paragonite) both of primary and secondary origin. The differences observed between the different lithotypes are related with the modal proportion of the principal minerals,with the presence or absence of certain accessory minerals ( turmaline, cordierite), with specific textural patterns, grain size and also with the richness in specific

Geochemical processes in marine salt deposits: Their significance and their implications in connection with disposal of radioactive waste within salt domes

Energy Technology Data Exchange (ETDEWEB)

Herrmann, A G [Goettingen Univ. (Germany, F.R.). Geochemisches Inst.

1980-01-01

Attempts to effect permanent disposal of radioactive wastes in marine evaporites should do nothing to disturb, either in the short or the long term, the present relative stability of such bodies of rock. It is necessary to take account of all of the geochemical and physico-chemical reactions known to have been involved in the processes which formed the evaporites before proceeding to an acceptable strategy for disposal of radionucleides. These processes can be represented as three kinds of metamorphism: 1. solution metamorphism, 2. thermal metamorphism, 3. dynamic metamorphism. In all of the evaporite occurrences in Germany such processes have been influential in altering, on occasion significantly, the primary mineralogical composition and have also promoted a considerable degree of transposition of material. Given similar geochemical and physico-chemical premises, these metamorphic processes could become effective now or in the future. It is therefore necessary to discuss the following criteria when examining salt domes as permanent repositories of highly radioactive substances: (1) Temperatures <= 90/sup 0/ +- 10/sup 0/C at the contact between waste containers and rock salt; (2) Temperatures <= 75/sup 0/C within zones of carnallite rocks; (3) Immobilisation of high-level waste in crystalline forms whenever possible; (4) Systems of additional safety barriers around the waste containers or the unreprocessed spent fuel elements. The geochemical and physical effectiveness of the barriers within an evaporite environment must be guaranteed. For example: Ni-Ti-alloys, corundum, ceramic, anhydrite.

Geochemical modeling of leaching from MSVI air-pollution-control residues

DEFF Research Database (Denmark)

Astrup, Thomas; Dijkstra, J.J.; Comans, R.N.J.

2006-01-01

This paper provides an improved understanding of the leaching behavior of waste incineration air-pollution-control (APC) residues in a long-term perspective. Leaching was investigated by a series of batch experiments reflecting leaching conditions after initial washout of highly soluble salts from...... residues. Leaching experiments were performed at a range of pH-values using carbonated and noncarbonated versions of two APC residues. The leaching data were evaluated by geochemical speciation modeling and discussed with respect to possible solubility control. The leaching of major elements as well...... of Al, Ba, Ca, Cr, Pb, S, Si, V, and Zn was found influenced by solubility control from Al2O3, Al(OH)3, Ba(S,Cr)O4 solid solutions, BaSO4, Ca6Al2(SO4)3(OH)12â26H2O, CaAl2Si4O12â2H2O, Ca-(OH)2, CaSiO3, CaSO4â2H2O, CaZn2(OH)6â2H2O, KAlSi2O6, PbCO3, PbCrO4, Pb2O3, Pb2V2O7, Pb3(VO4)2, ZnO, Zn2SiO4, and Zn...

Geochemical exploration for uranium

International Nuclear Information System (INIS)

1988-01-01

This Technical Report is designed mainly to introduce the methods and techniques of uranium geochemical exploration to exploration geologists who may not have had experience with geochemical exploration methods in their uranium programmes. The methods presented have been widely used in the uranium exploration industry for more than two decades. The intention has not been to produce an exhaustive, detailed manual, although detailed instructions are given for a field and laboratory data recording scheme and a satisfactory analytical method for the geochemical determination of uranium. Rather, the intention has been to introduce the concepts and methods of uranium exploration geochemistry in sufficient detail to guide the user in their effective use. Readers are advised to consult general references on geochemical exploration to increase their understanding of geochemical techniques for uranium

Monitoring active volcanoes: The geochemical approach

Directory of Open Access Journals (Sweden)

Takeshi Ohba

2011-06-01

Full Text Available

The geochemical surveillance of an active volcano aims to recognize possible signals that are related to changes in volcanic activity. Indeed, as a consequence of the magma rising inside the volcanic "plumbing system" and/or the refilling with new batches of magma, the dissolved volatiles in the magma are progressively released as a function of their relative solubilities. When approaching the surface, these fluids that are discharged during magma degassing can interact with shallow aquifers and/or can be released along the main volcano-tectonic structures. Under these conditions, the following main degassing processes represent strategic sites to be monitored.

The main purpose of this special volume is to collect papers that cover a wide range of topics in volcanic fluid geochemistry, which include geochemical characterization and geochemical monitoring of active volcanoes using different techniques and at different sites. Moreover, part of this volume has been dedicated to the new geochemistry tools.

Geochemical site-selection criteria for HLW repositories in Europe and North America

International Nuclear Information System (INIS)

Savage, David; Arthur, Randolph C.; Sasamoto, Hiroshi; Shibata, Masahiro; Yui, Mikazu

2000-01-01

Geochemical as well as socio-economic issues associated with the selection of potential sites to host a high-level nuclear waste repository have received considerable attention in repository programs in Europe (Belgium, Finland, France, Germany, Spain, Sweden, Switzerland and the U.K.) and North America (Canada and the United States). The objective of the present study is to summarize this international experience with particular emphasis on geochemical properties that factor into the adopted site-selection strategies. Results indicate that the geochemical properties of a site play a subordinate role, at best, to other geotechnical properties in the international site-selection approaches. In countries where geochemical properties are acknowledged in the site-selection approach, requirements are stated qualitatively and tend to focus on associated impacts on the stability of the engineered barrier system and on radionuclide transport. Site geochemical properties that are likely to control the long-term stability of geochemical conditions and radionuclide migration behavior are unspecified, however. This non-prescriptive approach may be reasonable for purposes of screening among potential sites, but a better understanding of site properties that are most important in controlling the long-term geochemical evolution of the site over a range of possible scenarios would enable the potential sites to be ranked in terms of their suitability to host a repository. (author)

Geochemical modelling: what phenomena are missing

International Nuclear Information System (INIS)

Jacquier, P.

1989-12-01

In the framework of safety assessment of radioactive waste disposal, retention phenomena are usually taken into account by the Kd concept. It is well recognized that this concept is not enough for safety assessment models, because of the several and strong assumptions which are involved in this kind of representation. One way to have a better representation of the retention phenomena, is to substitute for this Kd concept an explicit description of geochemical phenomena and then couple transport codes with geochemical codes in a fully or a two-step procedure. We use currently such codes, but the scope of this paper is to display the limits today of the geochemical modelling in connection with sites analysis for deep disposal. In this paper, we intend to give an overview of phenomena which are missing in the geochemical models, or which are not completely introduced in the models. We can distinguish, on one hand phenomena for which modelling concepts exist such as adsorption/desorption and, on the other hand, phenomena for which modelling concepts do not exist for the moment such as colloids, and complexation by polyelectrolyte solutions (organics). Moreover we have to take care of very low concentrations of radionuclides, which can be expected from the leaching processes in the repository. Under those conditions, some reactions may not occur. After a critical review of the involved phenomena, we intend to stress the main directions of the wishful evolution of the geochemical modelling. This evolution should improve substantially the quality of the above-mentioned site assessments

Behaviour of nature and technogenic radioisotopes in buried geochemical barriers

International Nuclear Information System (INIS)

Kuznetsov, V.A.; Onoshko, M.P.; Generalova, V.A.

1998-01-01

Behaviour of potassium 40, radium 226, thorium 232, strontium 90 and cesium 137 on geochemical barriers connected with buried soils and cut-off meander sediments of the Holocene age of the Sozh river valley are examined. Some sides of the barrier geochemical structure caused by syngeneic and epigenetic processes have been taken into consideration

Adjustment of geochemical background by robust multivariate statistics

Science.gov (United States)

Zhou, D.

1985-01-01

Conventional analyses of exploration geochemical data assume that the background is a constant or slowly changing value, equivalent to a plane or a smoothly curved surface. However, it is better to regard the geochemical background as a rugged surface, varying with changes in geology and environment. This rugged surface can be estimated from observed geological, geochemical and environmental properties by using multivariate statistics. A method of background adjustment was developed and applied to groundwater and stream sediment reconnaissance data collected from the Hot Springs Quadrangle, South Dakota, as part of the National Uranium Resource Evaluation (NURE) program. Source-rock lithology appears to be a dominant factor controlling the chemical composition of groundwater or stream sediments. The most efficacious adjustment procedure is to regress uranium concentration on selected geochemical and environmental variables for each lithologic unit, and then to delineate anomalies by a common threshold set as a multiple of the standard deviation of the combined residuals. Robust versions of regression and RQ-mode principal components analysis techniques were used rather than ordinary techniques to guard against distortion caused by outliers Anomalies delineated by this background adjustment procedure correspond with uranium prospects much better than do anomalies delineated by conventional procedures. The procedure should be applicable to geochemical exploration at different scales for other metals. ?? 1985.

Geochemical Modeling of Trivalent Chromium Migration in Saline-Sodic Soil during Lasagna Process: Impact on Soil Physicochemical Properties

Science.gov (United States)

Bukhari, Alaadin; Al-Malack, Muhammad H.; Mu'azu, Nuhu D.; Essa, Mohammed H.

2014-01-01

Trivalent Cr is one of the heavy metals that are difficult to be removed from soil using electrokinetic study because of its geochemical properties. High buffering capacity soil is expected to reduce the mobility of the trivalent Cr and subsequently reduce the remedial efficiency thereby complicating the remediation process. In this study, geochemical modeling and migration of trivalent Cr in saline-sodic soil (high buffering capacity and alkaline) during integrated electrokinetics-adsorption remediation, called the Lasagna process, were investigated. The remedial efficiency of trivalent Cr in addition to the impacts of the Lasagna process on the physicochemical properties of the soil was studied. Box-Behnken design was used to study the interaction effects of voltage gradient, initial contaminant concentration, and polarity reversal rate on the soil pH, electroosmotic volume, soil electrical conductivity, current, and remedial efficiency of trivalent Cr in saline-sodic soil that was artificially spiked with Cr, Cu, Cd, Pb, Hg, phenol, and kerosene. Overall desirability of 0.715 was attained at the following optimal conditions: voltage gradient 0.36 V/cm; polarity reversal rate 17.63 hr; soil pH 10.0. Under these conditions, the expected trivalent Cr remedial efficiency is 64.75 %. PMID:25152905

The outlier sample effects on multivariate statistical data processing geochemical stream sediment survey (Moghangegh region, North West of Iran)

International Nuclear Information System (INIS)

Ghanbari, Y.; Habibnia, A.; Memar, A.

2009-01-01

In geochemical stream sediment surveys in Moghangegh Region in north west of Iran, sheet 1:50,000, 152 samples were collected and after the analyze and processing of data, it revealed that Yb, Sc, Ni, Li, Eu, Cd, Co, as contents in one sample is far higher than other samples. After detecting this sample as an outlier sample, the effect of this sample on multivariate statistical data processing for destructive effects of outlier sample in geochemical exploration was investigated. Pearson and Spear man correlation coefficient methods and cluster analysis were used for multivariate studies and the scatter plot of some elements together the regression profiles are given in case of 152 and 151 samples and the results are compared. After investigation of multivariate statistical data processing results, it was realized that results of existence of outlier samples may appear as the following relations between elements: - true relation between two elements, which have no outlier frequency in the outlier sample. - false relation between two elements which one of them has outlier frequency in the outlier sample. - complete false relation between two elements which both have outlier frequency in the outlier sample

Thermal-hydraulic-geochemical coupled processes around disposed high level nuclear waste in deep granite hosted geological repositories: frontier areas of advanced groundwater research in India

International Nuclear Information System (INIS)

Bajpai, R.K.

2012-01-01

Indian policy for permanent disposal of high level nuclear wastes with radionuclide having very long half lives include their immobilization in a stable matrix i.e. glasses of suitable composition, its storage in high integrity steel canisters and subsequent disposal in suitable host rock like granites at a depth of 400-500m in stable geological set up. The site for such disposal facilities are selected after vigorous assessment of their stability implying an exhaustive site selection methodology based on a large number of criteria and attributes. In India, an area of about 70000 square kilometers occupied by granites has been subjected to such evaluation for generating comprehensive database on host rock parameters. The sites selected after such intensive analysis are expected to remain immune to processes like seismicity, volcanism, faulting, uplift, erosion, flooding etc. even in distant future spanning over tens of thousands of years. Nevertheless, groundwater has emerged as the only credible pathway through which disposed waste can eventually find its way to accessible biosphere. Hence groundwater research constitutes one of the most important aspects in demonstration of safety of such disposal. The disposed waste due to continuous emission of decay heat creates high temperature field around them with resultant increase in groundwater temperature in the vicinity. Hot groundwater on reacting with steel canisters, backfill clays and cement used around the disposed canister, produces geochemical environment characterized by altered Ph, Eh and groundwater compositions. Acceleration in geochemical interaction among waste-groundwater-clay-cement-granite often results in dissolution or precipitation reactions along the groundwater flow paths i.e. fractures with resultant increase or decrease in their permeability. Thus thermal, hydraulic and geochemical processes work interdependently around the disposed waste. These coupled processes also control the release and

Geochemical mapping study of Panjang island

International Nuclear Information System (INIS)

Sutisna; Sumardjo

2010-01-01

Impact of industrial and regional development are not only related to an improvement of socio-economic, but also to an environmental conservation and sustainable. This impact could be observed on a change of geochemical mapping before and after an operational of the industry. In the relation with a regional development and resources utilization, the geochemical mapping have been done in the aim to know a resources and an elemental distribution at Panjang island. In this research, ko-Instrumental Neutron Activation Analysis (k_0-INAA) have been applied in an elemental quantification on the geochemical mapping. Pencuplikan of geochemical sample have been carried out by using a grid systematic method with a sample density of about 10 sample per square kilometre involved 85 pencuplikan point. The geochemical sample of sediment and soil have been provided as a dry weight of 100 mesh. Internal quality control have done by using a number of Standard Reference Materials obtained from US. Geological Survey. Fifteen elements of Sc, Co, In, Rb, Mo, Ba, Ce, Nd, Eu, La, Yb, Th, U, lr and Hf contained in standard materials have been evaluated. The analysis result show that a relative standard deviation less than 11 %, except for Mo (13 %) and lr (26 %). Fourteen elements of Al, Br, Ca, Co, Eu, Fe, La, U, Na, Ce, Mn, As, Sc and Th have been mapped and presented in this paper. The major elements of Ca, Al and Fe, and minor elements of Mn, U and Sc are distributed at all region. The lanthanide elements of La, Ce and Eu have vary concentration and could be found at the middle to the north of the island. (author)

An integrated geophysical and geochemical exploration of critical zone weathering on opposing montane hillslope

Science.gov (United States)

Singha, K.; Navarre-Sitchler, A.; Bandler, A.; Pommer, R. E.; Novitsky, C. G.; Holbrook, S.; Moore, J.

2017-12-01

Quantifying coupled geochemical and hydrological properties and processes that operate in the critical zone is key to predicting rock weathering and subsequent transmission and storage of water in the shallow subsurface. Geophysical data have the potential to elucidate geochemical and hydrologic processes across landscapes over large spatial scales that are difficult to achieve with point measurements alone. Here, we explore the connections between weathering and fracturing, as measured from integrated geochemical and geophysical borehole data and seismic velocities on north- and south-facing aspects within one watershed in the Boulder Creek Critical Zone Observatory. We drilled eight boreholes up to 13 m deep on north- and south-facing aspects within Upper Gordon Gulch, and surface seismic refraction data were collected near these wells to explore depths of regolith and bedrock, as well as anisotropic characteristics of the subsurface material due to fracturing. Optical televiewer data were collected in these wells to infer the dominant direction of fracturing and fracture density in the near surface to corroborate with the seismic data. Geochemical samples were collected from four of these wells and a series of shallow soil pits for bulk chemistry, clay fraction, and exchangeable cation concentrations to identify depths of chemically altered saprolite. Seismic data show that depth to unweathered bedrock, as defined by p-wave seismic velocity, is slightly thicker on the north-facing slopes. Geochemical data suggest that the depth to the base of saprolite ranges from 3-5 m, consistent with a p-wave velocity value of 1200 m/s. Based on magnitude and anisotropy of p-wave velocities together with optical televiewer data, regolith on north-facing slopes is thought to be more fractured than south-facing slopes, while geochemical data indicate that position on the landscape is another important characteristic in determining depths of weathering. We explore the importance

Status report on geochemical modelling

International Nuclear Information System (INIS)

Read, D.

1991-12-01

This report describes the findings of a review undertaken on behalf of the project management group of the programme 'Endlagersicherheit in der Nachbetriebsphase' based at GSF-IfT (Forschungszentrum fuer Umwelt und Gesundheit - Institut fuer Tieflagerung) to establish the current status of research into the simulation of geochemical processes relevant to radiological assessment. The review is intended to contribute to Stage 1 of a strategy formulated to enhance the use of geochemical models in Germany. Emphasis has been placed on processes deemed to be of greatest relevance to performance assessment for a HLW-repository in a salt dome principally, speciation-solubility in high salinity solutions, complexation by natural organics and generation-transport of colloids. For each of these and other topics covered, a summary is given of fundamental concepts, theoretical representations and their limitations, highlighting, where appropriate, the advantages and disadvantages of alternative approaches. The availability of data to quantify any given representation is addressed, taking into account the need for information at elevated temperatures and pressures. Mass transfer is considered in terms of aqueous, particulate and gas-mediated transport, respectively. (orig.) [de

Quality assurance and quality control of geochemical data—A primer for the research scientist

Science.gov (United States)

Geboy, Nicholas J.; Engle, Mark A.

2011-01-01

Geochemistry is a constantly expanding science. More and more, scientists are employing geochemical tools to help answer questions about the Earth and earth system processes. Scientists may assume that the responsibility of examining and assessing the quality of the geochemical data they generate is not theirs but rather that of the analytical laboratories to which their samples have been submitted. This assumption may be partially based on knowledge about internal and external quality assurance and quality control (QA/QC) programs in which analytical laboratories typically participate. Or there may be a perceived lack of time or resources to adequately examine data quality. Regardless of the reason, the lack of QA/QC protocols can lead to the generation and publication of erroneous data. Because the interpretations drawn from the data are primary products to U.S. Geological Survey (USGS) stakeholders, the consequences of publishing erroneous results can be significant. The principal investigator of a scientific study ultimately is responsible for the quality and interpretation of the project's findings, and thus must also play a role in the understanding, implementation, and presentation of QA/QC information about the data. Although occasionally ignored, QA/QC protocols apply not only to procedures in the laboratory but also in the initial planning of a research study and throughout the life of the project. Many of the tenets of developing a sound QA/QC program or protocols also parallel the core concepts of developing a good study: What is the main objective of the study? Will the methods selected provide data of enough resolution to answer the hypothesis? How should samples be collected? Are there known or unknown artifacts or contamination sources in the sampling and analysis methods? Assessing data quality requires communication between the scientists responsible for designing the study and those collecting samples, analyzing samples, treating data, and

Methods for geochemical analysis

Science.gov (United States)

Baedecker, Philip A.

1987-01-01

The laboratories for analytical chemistry within the Geologic Division of the U.S. Geological Survey are administered by the Office of Mineral Resources. The laboratory analysts provide analytical support to those programs of the Geologic Division that require chemical information and conduct basic research in analytical and geochemical areas vital to the furtherance of Division program goals. Laboratories for research and geochemical analysis are maintained at the three major centers in Reston, Virginia, Denver, Colorado, and Menlo Park, California. The Division has an expertise in a broad spectrum of analytical techniques, and the analytical research is designed to advance the state of the art of existing techniques and to develop new methods of analysis in response to special problems in geochemical analysis. The geochemical research and analytical results are applied to the solution of fundamental geochemical problems relating to the origin of mineral deposits and fossil fuels, as well as to studies relating to the distribution of elements in varied geologic systems, the mechanisms by which they are transported, and their impact on the environment.

Geochemical processes of mercury in Wujiangdu and Dongfeng reservoirs, Guizhou, China

International Nuclear Information System (INIS)

Feng Xinbin; Jiang Hongmei; Qiu Guangle; Yan Haiyu; Li Guanghui; Li Zhonggen

2009-01-01

The geochemical processes of mercury in Dongfeng (DF) and Wujiangdu (WJD) reservoirs, which were constructed in 1992 and 1979, respectively in Wujiang River, which is the upper branch of Yangtze River were investigated. One sampling site was chosen upriver of 1 km from the dam for each reservoir. Three sampling campaigns were conducted at these sampling sites in December 2003, April 2004 and July 2004, respectively. The distributions of different mercury species in the water column, sediment, and sediment pore water were studied. We found that the sediment is the net source of both inorganic and MeHg to the water column for both reservoirs. The MeHg diffusion fluxes in WJD reservoir at all sampling campaigns were significantly higher than those in DF reservoir. Our study demonstrated that the high primary productivity in the reservoir produced elevated organic matter content that would favor the methylmercury production in sediment. - Surface sediment in the reservoirs is the active mercury methylating sites in the systems.

Chlorine isotopes potential as geo-chemical tracers

Digital Repository Service at National Institute of Oceanography (India)

Shirodkar, P.V.; Pradhan, U.K.; Banerjee, R.

The potential of chlorine isotopes as tracers of geo-chemical processes of earth and the oceans is highlighted based on systematic studies carried out in understanding the chlorine isotope fractionation mechanism, its constancy in seawater and its...

Heavy metal transport processes in surface water and groundwater. Geochemical and isotopic aspects

International Nuclear Information System (INIS)

Tricca, A.

1997-01-01

This work deals with the transport mechanisms of trace elements in natural aquatic systems. The experimental field is situated in the Upper Rhine Rift Valley because of the density and variety of its hydrological net. This study focused on three aspects: the isotopic tracing with Sr, Nd and O allowed to characterize the hydro-system. The 87 Sr/ 86 Sr and 143 Nd/ 144 Nd ratios show that the system is controlled by two natural end members a carbonate and a silicate one and a third end member of anthropogenic origin. The isotopic data allowed also to investigate the exchange processes between the dissolved and the particulate phases of the water samples. Because of their use in the industry and their very low concentrations in natural media, the Rare Earth Elements (REE) are very good tracers of anthropogenic contamination. Furthermore, due to their similar chemical properties with the actinides,they constitute excellent analogues to investigate the behaviour of fission products in the nature. In this study we determined the distribution of the REE within a river between the dissolved, the colloidal and the particulate phases. Among the REE of the suspended load, we distinguished between the exchangeable and the residual REE by means OF IN HCl leading experiments. The third topic is the investigation of uranium series disequilibrium using α-Spectrometry. The determination of ratios 234 U/ 238 U as well as of the activities short-lived radionuclides like 222 Rn, 224 Ra, 226 Ra, 228 Ra, 210 Po and 210 Pb have been performed. Their activities are controlled by chemical and physical parameters and depend also on the lithology of the source area. The combination of the three aspects provided relevant informations about the exchanges between the different water masses, about the transport mechanisms of the REE. Furthermore, the uranium series disequilibrium provided informations about the geochemical processes at a micro-scale. (author)

Effect of source integration on the geochemical fluxes from springs

International Nuclear Information System (INIS)

Frisbee, Marty D.; Phillips, Fred M.; White, Art F.; Campbell, Andrew R.; Liu, Fengjing

2013-01-01

Geochemical fluxes from watersheds are typically defined using mass-balance methods that essentially lump all weathering processes operative in a watershed into a single flux of solute mass measured in streamflow at the watershed outlet. However, it is important that we understand how weathering processes in different hydrological zones of a watershed (i.e., surface, unsaturated, and saturated zones) contribute to the total geochemical flux from the watershed. This capability will improve understanding of how geochemical fluxes from these different zones may change in response to climate change. Here, the geochemical flux from weathering processes occurring solely in the saturated zone is investigated. This task, however, remains exceedingly difficult due to the sparsity of subsurface sampling points, especially in large, remote, and/or undeveloped watersheds. In such cases, springflow is often assumed to be a proxy for groundwater (defined as water residing in fully saturated geologic formations). However, springflow generation may integrate different sources of water including, but not limited to, groundwater. The authors’ hypothesis is that long-term estimates of geochemical fluxes from groundwater using springflow proxies will be too large due to the integrative nature of springflow generation. Two conceptual models of springflow generation are tested using endmember mixing analyses (EMMA) on observations of spring chemistries and stable isotopic compositions in a large alpine watershed in the San Juan Mountains of southwestern Colorado. In the “total springflow” conceptual model, springflow is assumed to be 100% groundwater. In the “fractional springflow” conceptual model, springflow is assumed to be an integration of different sources of water (e.g., groundwater, unsaturated flow, preferential flow in the soil, etc.) and groundwater is only a fractional component. The results indicate that groundwater contributions in springflow range from 2% to 100

METHYL MERCURY PRODUCTION IN NATURAL-COLLECTED SEDIMENT WITH DIFFERENT GEOCHEMICAL PARAMETERS

Directory of Open Access Journals (Sweden)

Markus T. Lasut

2010-06-01

Full Text Available Production of methyl mercury (MeHg has been shown in laboratory experiments using mercuric chloride (HgCl2 compound released into natural-collected sediments with different geochemical conditions. While the HgCl2 concentration was 30 µl of 113 ppm of HgCl2, the geochemical conditions [pH, salinity, total organic content (TOC, sulfur] of sampled sediments were A: 8.20, 0.00 ppt, 1.97%, and 0.92 ppt, respectively; B: 7.90, 2.00 ppt, 4.69%, and 1.98 ppt, respectively; and C: 8.20, 24.00 ppt, 1.32 %, and 90.90 ppt, respectively. A control was set with no HgCl2. Samples and control were incubated in room temperature of 27 ± 1 °C. Observations were done along 9 days with interval of 3 days. While total Hg was measured using mercury analyzer with Cold Vapor-Atomic Absorbtion Spectrophometer (CV-AAS system, MeHg was measured by using a gas chromatograph with ECD detector after extracted by dithizone-sodium sulfide extraction method. The result shows that MeHg was found in both treatment and control experiments. The concentrations of the MeHg varied according to the geochemical condition of the sampled sediments. Peak production of MeHg occurred on the third day; however, the production was not significantly affected by the incubation time. Optimum production was found inversely related to the pH, in which highest and lowest the pH formed an ineffectively methylated mercury species. The TOC was significantly correlated to the optimum production. Salinity and sulfate contents were found not correlated to the optimum of MeHg production.   Keywords: Methyl mercury; methylation process; sediment; biogeochemistry

Geochemical and hydrologic controls on the mobilization of arsenic derived from herbicide application

International Nuclear Information System (INIS)

Fitzmaurice, Arthur G.; Bilgin, A. Azra; O'Day, Peggy A.; Illera, Virginia; Burris, David R.; Reisinger, H. James; Hering, Janet G.

2009-01-01

to JBF sediments may contribute to As sequestration, but As enrichment in JBF sediments within the plume (i.e., as compared with JBF sediments upgradient) was not observed. These results indicate that neither the persistence of As in the source area soils or the apparent stability of the plume of As-contaminated groundwater at this site can be explained by geochemical controls on As mobility. The absence of demonstrable geochemical bases for such observations suggests that possible hydrologic controls should be further investigated at this site.

Adaptive Multiscale Modeling of Geochemical Impacts on Fracture Evolution

Science.gov (United States)

Molins, S.; Trebotich, D.; Steefel, C. I.; Deng, H.

2016-12-01

Understanding fracture evolution is essential for many subsurface energy applications, including subsurface storage, shale gas production, fracking, CO2 sequestration, and geothermal energy extraction. Geochemical processes in particular play a significant role in the evolution of fractures through dissolution-driven widening, fines migration, and/or fracture sealing due to precipitation. One obstacle to understanding and exploiting geochemical fracture evolution is that it is a multiscale process. However, current geochemical modeling of fractures cannot capture this multi-scale nature of geochemical and mechanical impacts on fracture evolution, and is limited to either a continuum or pore-scale representation. Conventional continuum-scale models treat fractures as preferential flow paths, with their permeability evolving as a function (often, a cubic law) of the fracture aperture. This approach has the limitation that it oversimplifies flow within the fracture in its omission of pore scale effects while also assuming well-mixed conditions. More recently, pore-scale models along with advanced characterization techniques have allowed for accurate simulations of flow and reactive transport within the pore space (Molins et al., 2014, 2015). However, these models, even with high performance computing, are currently limited in their ability to treat tractable domain sizes (Steefel et al., 2013). Thus, there is a critical need to develop an adaptive modeling capability that can account for separate properties and processes, emergent and otherwise, in the fracture and the rock matrix at different spatial scales. Here we present an adaptive modeling capability that treats geochemical impacts on fracture evolution within a single multiscale framework. Model development makes use of the high performance simulation capability, Chombo-Crunch, leveraged by high resolution characterization and experiments. The modeling framework is based on the adaptive capability in Chombo

Geochemical evolution processes and water-quality observations based on results of the National Water-Quality Assessment Program in the San Antonio segment of the Edwards aquifer, 1996-2006

Science.gov (United States)

Musgrove, MaryLynn; Fahlquist, Lynne; Houston, Natalie A.; Lindgren, Richard J.; Ging, Patricia B.

2010-01-01

As part of the National Water-Quality Assessment Program, the U.S. Geological Survey collected and analyzed groundwater samples during 1996-2006 from the San Antonio segment of the Edwards aquifer of central Texas, a productive karst aquifer developed in Cretaceous-age carbonate rocks. These National Water-Quality Assessment Program studies provide an extensive dataset of groundwater geochemistry and water quality, consisting of 249 groundwater samples collected from 136 sites (wells and springs), including (1) wells completed in the shallow, unconfined, and urbanized part of the aquifer in the vicinity of San Antonio (shallow/urban unconfined category), (2) wells completed in the unconfined (outcrop area) part of the regional aquifer (unconfined category), and (3) wells completed in and springs discharging from the confined part of the regional aquifer (confined category). This report evaluates these data to assess geochemical evolution processes, including local- and regional-scale processes controlling groundwater geochemistry, and to make water-quality observations pertaining to sources and distribution of natural constituents and anthropogenic contaminants, the relation between geochemistry and hydrologic conditions, and groundwater age tracers and travel time. Implications for monitoring water-quality trends in karst are also discussed. Geochemical and isotopic data are useful tracers of recharge, groundwater flow, fluid mixing, and water-rock interaction processes that affect water quality. Sources of dissolved constituents to Edwards aquifer groundwater include dissolution of and geochemical interaction with overlying soils and calcite and dolomite minerals that compose the aquifer. Geochemical tracers such as magnesium to calcium and strontium to calcium ratios and strontium isotope compositions are used to evaluate and constrain progressive fluid-evolution processes. Molar ratios of magnesium to calcium and strontium to calcium in groundwater typically

Validation of the WATEQ4 geochemical model for uranium

International Nuclear Information System (INIS)

Krupka, K.M.; Jenne, E.A.; Deutsch, W.J.

1983-09-01

As part of the Geochemical Modeling and Nuclide/Rock/Groundwater Interactions Studies Program, a study was conducted to partially validate the WATEQ4 aqueous speciation-solubility geochemical model for uranium. The solubility controls determined with the WATEQ4 geochemical model were in excellent agreement with those laboratory studies in which the solids schoepite [UO 2 (OH) 2 . H 2 O], UO 2 (OH) 2 , and rutherfordine ((UO 2 CO 3 ) were identified as actual solubility controls for uranium. The results of modeling solution analyses from laboratory studies of uranyl phosphate solids, however, identified possible errors in the characterization of solids in the original solubility experiments. As part of this study, significant deficiencies in the WATEQ4 thermodynamic data base for uranium solutes and solids were corrected. Revisions included recalculation of selected uranium reactions. Additionally, thermodynamic data for the hydroxyl complexes of U(VI), including anionic (VI) species, were evaluated (to the extent permitted by the available data). Vanadium reactions were also added to the thermodynamic data base because uranium-vanadium solids can exist in natural ground-water systems. This study is only a partial validation of the WATEQ4 geochemical model because the available laboratory solubility studies do not cover the range of solid phases, alkaline pH values, and concentrations of inorganic complexing ligands needed to evaluate the potential solubility of uranium in ground waters associated with various proposed nuclear waste repositories. Further validation of this or other geochemical models for uranium will require careful determinations of uraninite solubility over the pH range of 7 to 10 under highly reducing conditions and of uranyl hydroxide and phosphate solubilities over the pH range of 7 to 10 under oxygenated conditions

Geochemical mapping using stream sediments in west-central Nigeria: Implications for environmental studies and mineral exploration in West Africa

International Nuclear Information System (INIS)

Lapworth, Dan J.; Knights, Katherine V.; Key, Roger M.; Johnson, Christopher C.; Ayoade, Emmanuel; Adekanmi, Michael A.; Arisekola, Tunde M.; Okunlola, Olugbenga A.; Backman, Birgitta; Eklund, Mikael; Everett, Paul A.; Lister, Robert T.; Ridgway, John; Watts, Michael J.; Kemp, Simon J.; Pitfield, Peter E.J.

2012-01-01

This paper provides an overview of regional geochemical mapping using stream sediments from central and south-western Nigeria. A total of 1569 stream sediment samples were collected and 54 major and trace elements determined by ICP-MS and Au, Pd and Pt by fire assay. Multivariate statistical techniques (e.g., correlation analysis and principal factor analysis) were used to explore the data, following appropriate data transformation, to understand the data structure, investigate underlying processes controlling spatial geochemical variability and identify element associations. Major geochemical variations are controlled by source geology and provenance, as well as chemical weathering and winnowing processes, more subtle variations are a result of land use and contamination from anthropogenic activity. This work has identified placer deposits of potential economic importance for Au, REE, Ta, Nb, U and Pt, as well as other primary metal deposits. Areas of higher As and Cr (>2 mg/kg and >70 mg/kg respectively) are associated with Mesozoic and younger coastal sediments in SW Nigeria. High stream sediment Zr concentrations (mean >0.2%), from proximal zircons derived from weathering of basement rocks, have important implications for sample preparation and subsequent analysis due to interferences. Associated heavy minerals enriched in high field strength elements, and notably rare earths, may also have important implications for understanding magmatic processes within the basement terrain of West Africa. This study provides important new background/baseline geochemical values for common geological domains in Nigeria (which extend across other parts of West Africa) for assessment of contamination from urban/industrial land use changes and mining activities. Regional stream sediment mapping is also able to provide important new information with applications across a number of sectors including agriculture, health, land use and planning.

Energy-constrained open-system magmatic processes IV: Geochemical, thermal and mass consequences of energy-constrained recharge, assimilation and fractional crystallization (EC-RAFC)

International Nuclear Information System (INIS)

Wendy A. Bohrson Department of Geological Sciences, Central Washington University, Ellensburg, Washington, 98926, USA; Frank J. Spera Institute for Crustal Studies and Department of Geological Sciences, University of California, Santa Barbara, California, 93106, USA

2003-01-01

A wealth of geochemical and petrological data provide evidence that the processes of fractional crystallization, assimilation, and magma recharge (replenishment) dominate the chemical signatures of many terrestrial igneous rocks. Previous work [Spera and Bohrson, 2001 ; Bohrson and Spera, 2001] has established the importance of integrating energy, species and mass conservation into simulations of complex magma chamber processes. An extended version of the energy-constrained formulation, Energy-Constrained Recharge, Assimilation, Fractional Crystallization (EC-RAFC), tracks mass and compositional variations of melt, cumulates, and enclaves in a magma body undergoing simultaneous recharge, assimilation, and fractional crystallization [Spera and Bohrson, 2002]. Because many EC-RAFC results are distinct from those predicted by extant RAFC formulations, the primary goal of this paper is to present a range of geochemical and mass relationships for selected cases that highlight issues relevant to modern petrology. Among the plethora of petrologic problems that have important, well-documented analogues in nature are the geochemical distinctions that arise when a magma body undergoes continuous versus episodic recharge, the connection between erupted magmas and associated cumulate bodies, the behavior of recharge-fractionation dominated systems (RFC), thermodynamic conditions that promote the formation of enclaves versus cumulates, and the conditions under which magma bodies may be described as chemically homogeneous. Investigation of the effects of continuous versus episodic recharge for mafic magma undergoing RAFC in the lower crust indicates that the resulting geochemical trends for melt and solids are sensitive to the intensity and composition of recharge, suggesting that EC-RAFC may be used as a tool to distinguish the nature of the recharge events. Compared to the record preserved in melts, the geochemical and mass characteristics of solids associated with particular

Role of soil geochemical and microbiological components on selenium behaviour in oxic and anoxic conditions

International Nuclear Information System (INIS)

Darcheville, O.

2008-09-01

Selenium (Se) is naturally present in the environment. Se is essential for living organisms at trace concentrations, but it becomes rapidly toxic with their increases. The 79 Se radioactive isotopes of Se, is found in nuclear wastes that may be buried in deep geological formations. In soil, Se exists in many forms and its mobility is affected by the redox potential and microbial activity. Very few studies have focused on Se behaviour at trace concentration. We have tried to distinguish the major abiotic geochemical and microbiological processes involved in the fate of trace selenite (Se(IV)) in a soil. The study was based on batch incubation in oxic or anoxic conditions of slurry suspension artificially contaminated with Se (IV) to 0.4 mg Se.kg -1 dry soil. The incubation involved sterilized and non-sterile soil samples with or without organic amendment to stimulate microbial activities. For each incubation, we followed the distribution of Se between solid, liquid and gaseous phases as well as the geochemical evolution of the solution, the composition of the atmosphere gas bottles and the soil microflora. The results showed that Se was relatively few mobile in the soil studied. Geochemical processes played a major role in controlling the Se mobility. Over time, some abiotic transformations in the solid phase contributed to increase the Se immobilisation. The microbiological processes contributed to this increase in the solid phase. Moreover, in oxic as in anoxic conditions, some microbial processes were responsible, to a lesser extent, for a dispersion of Se in the atmosphere by the production of volatile compounds. (author)

Application of cluster analysis to geochemical compositional data for identifying ore-related geochemical anomalies

Science.gov (United States)

Zhou, Shuguang; Zhou, Kefa; Wang, Jinlin; Yang, Genfang; Wang, Shanshan

2017-12-01

Cluster analysis is a well-known technique that is used to analyze various types of data. In this study, cluster analysis is applied to geochemical data that describe 1444 stream sediment samples collected in northwestern Xinjiang with a sample spacing of approximately 2 km. Three algorithms (the hierarchical, k-means, and fuzzy c-means algorithms) and six data transformation methods (the z-score standardization, ZST; the logarithmic transformation, LT; the additive log-ratio transformation, ALT; the centered log-ratio transformation, CLT; the isometric log-ratio transformation, ILT; and no transformation, NT) are compared in terms of their effects on the cluster analysis of the geochemical compositional data. The study shows that, on the one hand, the ZST does not affect the results of column- or variable-based (R-type) cluster analysis, whereas the other methods, including the LT, the ALT, and the CLT, have substantial effects on the results. On the other hand, the results of the row- or observation-based (Q-type) cluster analysis obtained from the geochemical data after applying NT and the ZST are relatively poor. However, we derive some improved results from the geochemical data after applying the CLT, the ILT, the LT, and the ALT. Moreover, the k-means and fuzzy c-means clustering algorithms are more reliable than the hierarchical algorithm when they are used to cluster the geochemical data. We apply cluster analysis to the geochemical data to explore for Au deposits within the study area, and we obtain a good correlation between the results retrieved by combining the CLT or the ILT with the k-means or fuzzy c-means algorithms and the potential zones of Au mineralization. Therefore, we suggest that the combination of the CLT or the ILT with the k-means or fuzzy c-means algorithms is an effective tool to identify potential zones of mineralization from geochemical data.

Geochemical characterization of Parana Basin volcanic rocks: petrogenetic implications

International Nuclear Information System (INIS)

Marques, L.S.

1988-01-01

A detailed study of the geochemical characteristics of Parana Basin volcanic rocks is presented. The results are based on the analyses of major and trace elements of 158 samples. Ninety three of these volcanic samples belong to 8 flow sequences from Rio Grande do Sul and Santa Catarina States. The remaining sixty five samples are distributed over the entire basin. In order to study the influence of crustal contamination processes in changing chemical characteristics of the volcanic rocks, 47 samples representative of the crystalline basement of the southern and southeastern Parana Basin were also analysed. Several petrogenetic models were tested to explain the compocional variability of the volcanic rocks, in particular those of southern region. The results obtained sugest an assimilation-fractional crystallization process as viable to explain the differences of both the chemical characteristics and Sr isotope initial ratios observed in basic and intermediate rocks. A model involving melting processes of basic material, trapped at the base of the crust, with composition similar to low and high TiO 2 basalts appears to be a possibility to originate the Palmas and Chapeco acid melts, respectively. The study of ''uncontaminated'' or poorly contaminated low TiO 2 basic rocks from the southern, central and northern regions shows the existence of significant differences in the geochemical charactetistics according to their geographical occurrence. A similar geochemical diversity is also observed in high TiO 2 basalts and Chapeco volcanics. Differences in incompatible element ratios between low and high TiO 2 ''uncontaminated'' or poorly contaminated basalts suggest that they could have been produced by different degrees of melting in a garnet peridotite source. Geochemical and isotopic (Sr and Nd) data also support the view that basalts from northern and southern regions of Parana Basin originated from mantle source with different composition. (author) [pt

Geochemical patterns and microbial contribution to iron plaque formation in the rice plant rhizosphere

Science.gov (United States)

Maisch, Markus; Murata, Chihiro; Unger, Julia; Kappler, Andreas; Schmidt, Caroline

2015-04-01

Rice is the major food source for more than half of the world population and 80 percent of the worldwide rice cultivation is performed on water logged paddy soils. The establishment of reducing conditions in the soil and across the soil-water interface not only stimulates the microbial production and release of the greenhouse gas methane. These settings also create optimal conditions for microbial iron(III) reduction and therefore saturate the system with reduced ferrous iron. Through the reduction and dissolution of ferric minerals that are characterized by their high surface activity, sorbed nutrients and contaminants (e.g. arsenic) will be mobilized and are thus available for uptake by plants. Rice plants have evolved a strategy to release oxygen from their roots in order to prevent iron toxification in highly ferrous environments. The release of oxygen to the reduced paddy soil causes ferric iron plaque formation on the rice roots and finally increases the sorption capacity for toxic metals. To this date the geochemical and microbiological processes that control the formation of iron plaque are not deciphered. It has been hypothesized that iron(II)-oxidizing bacteria play a potential role in the iron(III) mineral formation along the roots. However, not much is known about the actual processes, mineral products, and geochemical gradients that establish within the rhizosphere. In the present study we have developed a growth set-up that allows the co-cultivation of rice plants and iron(II)-oxidizing bacteria, as well as the visual observation and in situ measurement of geochemical parameters. Oxygen and dissolved iron(II) gradients have been measured using microelectrodes and show geochemical hot spots that offer optimal growth conditions for microaerophilic iron(II) oxidizers. First mineral identification attempts of iron plaque have been performed using Mössbauer spectroscopy and microscopy. The obtained results on mineraology and crystallinity have been

Lessons learned from the Febex in situ test: geochemical processes associated to the microbial degradation and gas generation

International Nuclear Information System (INIS)

Fernandez, A. M.; Sanchez, D.M.; Melon, A.; Mingarro, M.; Wieczorek, K.

2012-01-01

Document available in extended abstract form only. Compacted bentonites are considered as backfill and sealing material in most high-level radioactive waste disposal (HLW) concepts because of their physico-chemical properties. Although they are very stable in their original natural ambient, any change in the physico-chemical, geochemical and mineralogical conditions may influence in their functions. Therefore, numerous studies have been performed during years in order to evaluate the bentonite barrier behaviour affected by thermo-hydro-mechanical and geochemical processes in tests at different scales. One of the key parameters in the safety assessment of a nuclear waste repository is the redox conditions of the bentonite pore water in the near field, due to their effect on the mobility and sorption of a lot of radionuclides. Among the factors that influence the Eh of the pore water are: a) the amount of oxygen in the barrier and in the clay-rocks, b) the type of existing minerals sensible to the redox potential, c) the production of radiolytic oxidants and reductants, d) the type and rate of the metal corrosion, f) the existence of organic matter, and e) the presence and viability of micro-organisms. However, the microbiological processes have not been taken into account during a lot of years because it is was thought that the microbial growth and activity at repository conditions are improbable due to: the low water activity as a consequence of the heat and the pore water salinity, the reduced space for their growth due to the compaction degree and swelling of the bentonite, etc. Different studies have shown that the microorganisms stop their activity at a w 2 MPa, low availability of water, small pore size 3 or a pore water salinity > 100 g NaCl/L. Nevertheless, during the transitory phase of the bentonite saturation, some modifications occur in the salinity of the pore water, the initial dry densities due to the hydration process, the swelling pressures, and the

Geology of pre-Dakota uranium geochemical cell, sec. 13, T. 16 N., R. 17 W., Church Rock area, McKinley County

International Nuclear Information System (INIS)

Peterson, R.J.

1980-01-01

Exploration drilling on sec. 13, T. 16 N., R. 17 W., McKinley County, New Mexico, has defined uranium deposits within the Westwater Canyon Member of the Morrison Formation (Jurassic). Elongate, tabular, redistributed deposits were formed peripherally along the zones of highest transmissivity of the northeast-trending Westwater Canyon fluvial system by a Jurassic-Cretaceous geochemical cell. Strongly reducing conditions, which existed locally in the channel-margin areas owing to the presence of organic materials, were the primary ore control. Evidence that this major redistribution process took place in pre-Dakota time is the bleaching of the Westwater Canyon Sandstone by Dakota swamps is superimposed on older oxidation, and the primary mineralization above the Jurassic-Cretaceous water table was not affected by the geochemical-cell redistribution process

Geochemical porosity values obtained in core samples from different clay-rocks

International Nuclear Information System (INIS)

Fernandez, A.M.

2010-01-01

Document available in extended abstract form only. Argillaceous formations of low permeability are considered in many countries as potential host rocks for the disposal of high level radioactive wastes (HLRW). In order to determine their suitability for waste disposal, evaluations of the hydro-geochemistry and transport mechanisms from such geologic formations to the biosphere must be undertaken. One of the key questions about radionuclide diffusion and retention is to know the chemistry and chemical reactions and sorption processes that will occur in the rock and their effects on radionuclide mobility. In this context, the knowledge of the pore water chemistry is essential for performance assessment purposes. This information allows to establish a reliable model for the main water-rock interactions, which control the physico-chemical parameters and the chemistry of the major elements of the system. An important issue in order to model the pore water chemistry in clayey media is to determine the respective volume accessible to cations and anions, i.e, the amount of water actually available for chemical reactions/solute transport. This amount is usually referred as accessible porosity or geochemical porosity. By using the anion inventories, i.e. the anion content obtained from aqueous leaching, and assuming that all Cl - , Br - and SO4 2- leached in the aqueous extracts originates from pore water, the concentration of a conservative ion can be converted into the real pore water concentration if the accessible porosity is known. In this work, the accessible porosity or geochemical porosity has been determined in core samples belonging to four different formations: Boom Clay from Hades URL (Belgium, BE), Opalinus Clay from Mont Terri (Switzerland, CH), and Callovo-Oxfordian argillite from Bure URL (France, FR). The geochemical or chloride porosity was defined as the ratio between the pore water volume containing Cl-bearing pore water and the total volume of a sample

Proceedings of the workshop on geochemical modeling

International Nuclear Information System (INIS)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices

Proceedings of the workshop on geochemical modeling

Energy Technology Data Exchange (ETDEWEB)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices.

Development of a Model of Geophysical and Geochemical Controls on Abiotic Carbon Cycling on Earth-Like Planets

Science.gov (United States)

Neveu, M.; Felton, R.; Domagal-Goldman, S. D.; Desch, S. J.; Arney, G. N.

2017-12-01

About 20 Earth-sized planets (0.6-1.6 Earth masses and radii) have now been discovered beyond our solar system [1]. Although such planets are prime targets in the upcoming search for atmospheric biosignatures, their composition, geology, and climate are essentially unconstrained. Yet, developing an understanding of how these factors influence planetary evolution through time and space is essential to establishing abiotic backgrounds against which any deviations can provide evidence for biological activity. To this end, we are building coupled geophysical-geochemical models of abiotic carbon cycling on such planets. Our models are controlled by atmospheric factors such as temperature and composition, and compute interior inputs to atmospheric species. They account for crustal weathering, ocean-atmosphere equilibria, and exchange with the deep interior as a function of planet composition and size (and, eventually, age).Planets in other solar systems differ from the Earth not only in their bulk physical properties, but also likely in their bulk chemical composition [2], which influences key parameters such as the vigor of mantle convection and the near-surface redox state. Therefore, simulating how variations in such parameters affect carbon cycling requires us to simulate the above processes from first principles, rather than by using arbitrary parameterizations derived from observations as is often done with models of carbon cycling on Earth [3] or extrapolations thereof [4]. As a first step, we have developed a kinetic model of crustal weathering using the PHREEQC code [5] and kinetic data from [6]. We will present the ability of such a model to replicate Earth's carbon cycle using, for the time being, parameterizations for surface-interior-atmosphere exchange processes such as volcanism (e.g., [7]).[1] exoplanet.eu, 7/28/2017.[2] Young et al. (2014) Astrobiology 14, 603-626.[3] Lerman & Wu (2008) Kinetics of Global Geochemical Cycles. In Kinetics of Water

Experimental insights into geochemical changes in hydraulically fractured Marcellus Shale

International Nuclear Information System (INIS)

Marcon, Virginia; Joseph, Craig; Carter, Kimberly E.; Hedges, Sheila W.; Lopano, Christina L.; Guthrie, George D.; Hakala, J. Alexandra

2017-01-01

Hydraulic fracturing applied to organic-rich shales has significantly increased the recoverable volume of methane available for U.S. energy consumption. Fluid-shale reactions in the reservoir may affect long-term reservoir productivity and waste management needs through changes to fracture mineral composition and produced fluid chemical composition. We performed laboratory experiments with Marcellus Shale and lab-generated hydraulic fracturing fluid at elevated pressures and temperatures to evaluate mineral reactions and the release of trace elements into solution. Results from the experiment containing fracturing chemicals show evidence for clay and carbonate dissolution, secondary clay and anhydrite precipitation, and early-stage (24–48 h) fluid enrichment of certain elements followed by depletion in later stages (i.e. Al, Cd, Co, Cr, Cu, Ni, Sc, Zn). Other elements such as As, Fe, Mn, Sr, and Y increased in concentration and remained elevated throughout the duration of the experiment with fracturing fluid. Geochemical modeling of experimental fluid data indicates primary clay dissolution, and secondary formation of smectites and barite, after reaction with fracturing fluid. Changes in aqueous organic composition were observed, indicating organic additives may be chemically transformed or sequestered by the formation after hydraulic fracturing. The NaCl concentrations in our fluids are similar to measured concentrations in Marcellus Shale produced waters, showing that these experiments are representative of reservoir fluid chemistries and can provide insight on geochemical reactions that occur in the field. These results can be applied towards evaluating the evolution of hydraulically-fractured reservoirs, and towards understanding geochemical processes that control the composition of produced water from unconventional shales. - Highlights: • Metal concentrations could be at their peak in produced waters recovered 24–48 after fracturing. • Carbonate

Geochemical computer codes. A review

International Nuclear Information System (INIS)

Andersson, K.

1987-01-01

In this report a review of available codes is performed and some code intercomparisons are also discussed. The number of codes treating natural waters (groundwater, lake water, sea water) is large. Most geochemical computer codes treat equilibrium conditions, although some codes with kinetic capability are available. A geochemical equilibrium model consists of a computer code, solving a set of equations by some numerical method and a data base, consisting of thermodynamic data required for the calculations. There are some codes which treat coupled geochemical and transport modeling. Some of these codes solve the equilibrium and transport equations simultaneously while other solve the equations separately from each other. The coupled codes require a large computer capacity and have thus as yet limited use. Three code intercomparisons have been found in literature. It may be concluded that there are many codes available for geochemical calculations but most of them require a user that us quite familiar with the code. The user also has to know the geochemical system in order to judge the reliability of the results. A high quality data base is necessary to obtain a reliable result. The best results may be expected for the major species of natural waters. For more complicated problems, including trace elements, precipitation/dissolution, adsorption, etc., the results seem to be less reliable. (With 44 refs.) (author)

Manual hierarchical clustering of regional geochemical data using a Bayesian finite mixture model

International Nuclear Information System (INIS)

Ellefsen, Karl J.; Smith, David B.

2016-01-01

Interpretation of regional scale, multivariate geochemical data is aided by a statistical technique called “clustering.” We investigate a particular clustering procedure by applying it to geochemical data collected in the State of Colorado, United States of America. The clustering procedure partitions the field samples for the entire survey area into two clusters. The field samples in each cluster are partitioned again to create two subclusters, and so on. This manual procedure generates a hierarchy of clusters, and the different levels of the hierarchy show geochemical and geological processes occurring at different spatial scales. Although there are many different clustering methods, we use Bayesian finite mixture modeling with two probability distributions, which yields two clusters. The model parameters are estimated with Hamiltonian Monte Carlo sampling of the posterior probability density function, which usually has multiple modes. Each mode has its own set of model parameters; each set is checked to ensure that it is consistent both with the data and with independent geologic knowledge. The set of model parameters that is most consistent with the independent geologic knowledge is selected for detailed interpretation and partitioning of the field samples. - Highlights: • We evaluate a clustering procedure by applying it to geochemical data. • The procedure generates a hierarchy of clusters. • Different levels of the hierarchy show geochemical processes at different spatial scales. • The clustering method is Bayesian finite mixture modeling. • Model parameters are estimated with Hamiltonian Monte Carlo sampling.

Geochemical prospecting for uranium and thorium deposits

International Nuclear Information System (INIS)

Boyle, R.W.

1980-01-01

A brief review of analytical geochemical prospecting methods for uranium and thorium is given excluding radiometric techniques, except those utilized in the determination of radon. The indicator (pathfinder) elements useful in geochemical surveys are listed for each of the types of known uranium and thorium deposits; this is followed by sections on analytical geochemical surveys based on rocks (lithochemical surveys), unconsolidated materials (pedochemical surveys), natural waters and sediments (hydrochemical surveys), biological materials (biogeochemical surveys) and gases (atmochemical surveys). All of the analytical geochemical methods are applicable in prospecting for thorium and uranium, particularly where radiometric methods fail due to attenuation by overburden, water, deep leaching and so on. Efficiency in the discovery of uranium and/or thorium orebodies is promoted by an integrated methods approach employing geological pattern recognition in the localization of deposits, analytical geochemical surveys, and radiometric surveys. (author)

A Geochemical Reaction Model for Titration of Contaminated Soil and Groundwater at the Oak Ridge Reservation

Science.gov (United States)

Zhang, F.; Parker, J. C.; Gu, B.; Luo, W.; Brooks, S. C.; Spalding, B. P.; Jardine, P. M.; Watson, D. B.

2007-12-01

This study investigates geochemical reactions during titration of contaminated soil and groundwater at the Oak Ridge Reservation in eastern Tennessee. The soils and groundwater exhibits low pH and high concentrations of aluminum, calcium, magnesium, manganese, various trace metals such as nickel and cobalt, and radionuclides such as uranium and technetium. The mobility of many of the contaminant species diminishes with increasing pH. However, base additions to increase pH are strongly buffered by various precipitation/dissolution and adsorption/desorption reactions. The ability to predict acid-base behavior and associated geochemical effects is thus critical to evaluate remediation performance of pH manipulation strategies. This study was undertaken to develop a practical but generally applicable geochemical model to predict aqueous and solid-phase speciation during soil and groundwater titration. To model titration in the presence of aquifer solids, an approach proposed by Spalding and Spalding (2001) was utilized, which treats aquifer solids as a polyprotic acid. Previous studies have shown that Fe and Al-oxyhydroxides strongly sorb dissolved Ni, U and Tc species. In this study, since the total Fe concentration is much smaller than that of Al, only ion exchange reactions associated with Al hydroxides are considered. An equilibrium reaction model that includes aqueous complexation, precipitation, ion exchange, and soil buffering reactions was developed and implemented in the code HydroGeoChem 5.0 (HGC5). Comparison of model results with experimental titration curves for contaminated groundwater alone and for soil- water systems indicated close agreement. This study is expected to facilitate field-scale modeling of geochemical processes under conditions with highly variable pH to develop practical methods to control contaminant mobility at geochemically complex sites.

SYNROC process. A geochemical approach to nuclear waste immobilization

Energy Technology Data Exchange (ETDEWEB)

Ringwood, A E; Kesson, S E; Ware, N G; Hibberson, W O; Major, A [Australian National Univ., Canberra. Research School of Earth Sciences

1979-08-01

The SYNROC process is proposed to immobilize high-level wastes as dilute solid solutions in the constituent minerals of a synthetic rock formed from a mixture of oxides. New modification of the SYNROC was developed. Experiments showed that the entire spectra of high-level waste elements can be incorporated in the crystal lattices of Ba-hollandite, perovskite and zirconolite. This titanate assemblage has been proved to be exceptionally resistant to hydrothermal leaching, and in this respect, amongst others, it is demonstrably superior to alternative ceramic waste forms and to borosilicate glasses. The relative stability of various waste forms was compared in hydrothermal leaching experiments using both pure water and 10 w/o NaCl solution. Borosilicate glasses were almost completely decomposed and disintegrated after only 24 hours at 350 deg C and 1000 bars, and the extensive loss of hazardous high-level waste elements occurred. The phase pollucite in ceramic waste forms began to decompose at 400 deg C. The hollandite-perovskite-zirconolite SYNROC assemblage was proved to be exceptionally resistant to leaching, surviving invariably the extreme conditions up to 900 deg C and 5000 bars. Geochemical studies of the naturally-occurring minerals containing radwaste elements are relevant to the problem of radiation damage to SYNROC phases. These imply that the 2-particle flux in SYNROC is unlikely to be enough to impair the ability to immobilize radwaste for the required period. The production of SYNROC is explained in detail. The SYNROC phases have the structures analogous to the natural minerals which have survived a variety of geological conditions for millions of years while retaining certain high-level waste elements in their crystal lattices.

Geochemical, hydrological and biological cycling of energy residuals. Research plan: subsurface transport program

International Nuclear Information System (INIS)

Wobber, F.J.

1985-09-01

Because natural processes associated with the release and the transport of organic compounds, trace metals, and radionuclides are incompletely understood, research in this area is critical if the long term scientific uncertainties about contaminant transport are to be resolved. The processes that control mobilization and attenuation of energy residuals in soils and geological strata, their hydrological transport to and within ground water regimes, and their accumulation in biological systems require research attention. A summary of DOE's core research program is described. It is designed to provide a base of fundamental scientific information so that the geochemical hydrological, and biophysical mechanics that contribute to the transport and long term fate of energy related contaminants in natural systems can be understood

Role of geochemical background at evaluation of investment attractiveness of recreational territories

Directory of Open Access Journals (Sweden)

Vdovina Ol'ga Konstantinovna

2014-09-01

Full Text Available The article shows the role of natural geochemical background when estimating investment attractiveness of recreational areas. It is noted, that geochemical background influence on people's sickness rate isn't considered now. Though it's understood, that even insignificant increase of geochemical background in relation to percentage abundance of Earth crest may lead to endemic diseases of people, animals and plants. An indicator of geochemical endemicity areas was proposed for assessing the impact of storage elements and of a lack of geological environment on human health. Thanks to this measure, and taking into account landscape features of the area, the authors allocated lands, dangerous and potentially dangerous in terms of endemicity. The importance of ratings was achieved by the use of those factors that could have a great influence on the cost of land development. This includes, first of all, the factors that affect population health, and economic and geographic factors that minimize the cost of the territory development and the factors that give rise to financial risks and risks of human losses. The main risk factors include: potential ecological and geochemical risk; high absolute heights, development and activity of dangerous geological processes and phenomena. Systemacity of researches was reached by using factors, that characterize the object from different aspects; readiness of area infrastructure to its exploration and possible risks. Objectivity was achieved by the use of figures obtained from the results of geochemical and engineering surveys with their metrological support.

Isotopic and geochemical tracers for fingerprinting process-affected waters in the oil sands industry: a pilot study

Energy Technology Data Exchange (ETDEWEB)

Gibson, J.J.; Birks, S.J.; Moncur, M.; Yi, Y.; Tattrie, K.; Jasechko, S.; Richardson, K.; Eby, P. [Alberta Innovates - Technology Futures (Canada)

2011-04-15

During 2009 and 2010, Alberta Innovates - Technology Futures carried out a pilot study for Alberta Environment to examine the possibility of labeling process affected water from oil sands operations with isotropic and geochemical tracers. For the study, 3 oil sands operators furnished logistical support and personnel, 39 samples were gathered and several isotope tracers were measured. In addition, geotechnical analyses were performed and the presence of organic compounds in the samples was scanned using Fourier transform ion cyclotron resonance mass spectrometry. Results showed that the selected tracers were able to label water sources in some locations, however they cannot be used as a universal method and a case by case approach needs to be adopted. This study pointed out that Fourier transform ion cyclotron resonance mass spectrometry is the best way to construct a dataset for use in identification of process affected waters.

Geochemical correlations between uranium and other components in U-bearing formations of Ogcheon belt

International Nuclear Information System (INIS)

Lee, M.S.; Chon, H.T.

1980-01-01

Some components in uranium-bearing formations which consist mainly of black shale, slate and low grade coal-bearing formation of Ogcheon Belt were processed statistically in order to find out the geochemical correlations with uranium. Geochemical enrichment of uranium, vanadium and molybdenum in low grade coal-bearing formations and surrounding rocks is remarkable in the studied area. Geochemical correlation coefficient of uranium and molybdenum in the rocks displays about 0.6 and that of uranium and fixed carbon about 0.4. Uranium and vanadium in uranium-bearing low grade coals denote very high correlation with fixed carbon, which is considered to be responsible for enrichment of metallic elements, especially molybdenum. Close geochemical correlation of uranium-molybdenum couple in the rocks can be applied as a competent exploration guide to low grade uranium deposits of this area. (author)

Geophysical Monitoring of Coupled Microbial and Geochemical Processes During Stimulated Subsurface Bioremediation

International Nuclear Information System (INIS)

Williams, Kenneth H.; Kemna, Andreas; Wilkins, Michael J.; Druhan, Jennifer L.; Arntzen, Evan V.; N'Guessan, A. Lucie; Long, Philip E.; Hubbard, Susan S.; Banfield, Jillian F.

2009-01-01

Understanding how microorganisms alter their physical and chemical environment during bioremediation is hindered by our inability to resolve subsurface microbial activity with high spatial resolution. Here we demonstrate the use of a minimally invasive geophysical technique to monitor stimulated microbial activity during acetate amendment in an aquifer near Rifle, Colorado. During electrical induced polarization (IP) measurements, spatiotemporal variations in the phase response between imposed electric current and the resultant electric field correlated with changes in groundwater geochemistry accompanying stimulated iron and sulfate reduction and sulfide mineral precipitation. The magnitude of the phase response varied with measurement frequency (0.125 and 1 Hz) and was dependent upon the dominant metabolic process. The spectral effect was corroborated using a biostimulated column experiment containing Rifle sediments and groundwater. Fluids and sediments recovered from regions exhibiting an anomalous phase response were enriched in Fe(II), dissolved sulfide, and cell-associated FeS nanoparticles. The accumulation of mineral precipitates and electroactive ions altered the ability of pore fluids to conduct electrical charge, accounting for the anomalous IP response and revealing the usefulness of multifrequency IP measurements for monitoring mineralogical and geochemical changes accompanying stimulated subsurface bioremediation

Geochemical Parameters Required from the SKB Site Characterisation Programme

International Nuclear Information System (INIS)

Bath, Adrian

2002-01-01

SKB has described its approach to site characterisation in a number of Technical Reports. One of the scientific topics in which specific information requirements and priorities are set out is geochemistry. This report for SKI examines critically whether the geochemical parameters identified in the SKB programme documents will be adequate for safety and regulatory requirements. It also examines some of the details of parameter requirements and interpretation tools that will be necessary to convert site investigation data into knowledge about chemical conditions and groundwater movements. The SKB strategy for geochemical data focuses on a small number of 'suitability indicators', primarily dissolved oxygen, pH and salinity. Their parameter requirements aim to assess those primary characteristics, as well as to acquire a wider range of data that will support those assessments and provide a broader understanding of candidate areas. An initial observation in this review that, though it is a primary suitability indicator, dissolved oxygen apparently will not be measured and instead will be inferred from other redox indicators. This raises a number of issues about sampling and monitoring measures, analytical data reliability and sensitivity, and the degree of confidence in geochemical understanding. A geochemical programme involves reconnaissance by desk study and acquisition of new data at levels of details that are appropriate to the stage of site investigations. As early as possible, a conceptual model of a candidate area should help to define the objectives of geochemical measurements on both rock and groundwater samples. It is recommended that parameters requirements should be defined and considered not only in terms of isolated measurements but more in terms of addressing broader objectives that relate to safety and also to geoscientific understanding. The safety priorities remain (e.g. dissolved oxygen) but will then be supported by an understanding of processes

Geochemical Parameters Required from the SKB Site Characterisation Programme

Energy Technology Data Exchange (ETDEWEB)

Bath, Adrian [Intellisci Ltd., Loughborough (United Kingdom)

2002-01-01

processes. This approach will also help to clarify the rationale for taking samples and making particular measurements and will indicate the tolerances in terms of data error and interpretative uncertainty. Geochemical parameters that are required from rock, mineral, water and dissolved gas samples are listed and discussed along with the reasons for requiring the data. Measures that need to be taken to optimise the quality and representativeness of samples are also discussed because these are paramount in determining the ultimate reliability of data. Finally, interpretative tools that are used to convert raw data into knowledge and confidence in understanding of processes have been briefly considered. These may have additional 'supporting' data requirements and also need to be critically reviewed for their applicability and for the robustness of the conceptual models on which they are based.

GEOBASI: The geochemical Database of Tuscany Region (Italy

Directory of Open Access Journals (Sweden)

Brunella Raco

2015-03-01

statistical and geostatistical methods, using open source software (QGIS and R to support the process of evaluation of the geochemical baseline.

Geochemical Anomalies in the Sediments of Lake Druksiai

International Nuclear Information System (INIS)

Kleinas, A.

1999-01-01

In order to evaluate the impact of Ignalina Nuclear Power Plant (NPP) on natural processes in Lake Druksiai and accumulation of pollutants, in 19931997, carrying on the state scientific program, the Marine Geochemistry Division of the Institute of Geography performed lithological geochemical mapping of lake bottom sediments on a scale of 1 .50 000. The results obtained enabled to distinguish zones of higher anthropogenous geochemical load, where geochemical anomalies of pollutants, including oil hydrocarbons and heavy metals, had been taken into account. Applying concentration coefficients for oil hydrocarbons and heavy metals (Cr, Cu, Ni, Pb, and Zn) and their natural background, the attempt was made to differentiate natural and technogenous components in the geochemical anomalies As expected, the finer sediments -aleurite-pelite mud - showed amounts of oil hydrocarbons and heavy metals being 12.1 times higher than in fine sand - the most coarse of the sediments studied Sediments with organic mater exceeding 20% contained 11.7 times more pollutants than those with organic matter below 1 .5%. Calculations of concentration coefficients (CC) showed no elements in no stations exceeded 10 - the sediments did not reach the category of high pollution However, in many sites, the coefficients exceeded values of 1-2, thus, showing sediments attributable to the categories of weakly polluted or just polluted. Mapping model done by GIS methods (by superimposing schemes of pollutant CCs distribution in the lake and summing them) for geochemical anomalies two derivative map-schemes were obtained for oil hydrocarbons and heavy metals. They showed that clean sediments cover just 24.75% (according to the pollutant background for soil types) and 12.35% (according to the organic matter background for its amount intervals) lake bottom area. Zones slightly polluted by an element at least cover 69.7 and 80.29% of lake area, correspondingly; whereas zones slightly polluted by all

Geochemical analysis of the sealing system. Technical Report to work package 9.1.2. Preliminary safety case of the Gorleben site (VSG)

Energy Technology Data Exchange (ETDEWEB)

Xie, Mingliang; Herbert, Horst-Juergen

2012-02-15

The geochemical reaction simulation of ground water and brines with sealing materials for a proposed repository at the Gorleben site is a task under the framework of the VSG project. The calculations presented in this report are aimed to provide a preliminary evaluation of the geochemical stability of three potential engineering barrier materials foreseen in the shaft sealing system in case of groundwater and brine intrusion. The long-term stability of these materials is a key issue for the sealing function of the shaft seals. This is governed by many factors such as geotechnical, hydraulic and geochemical processes. In order to better understand the potential effect of geochemical processes on the long-term properties of these sealing materials, geochemical simulations of the potential interactions between groundwater and brine and shaft sealing materials were performed.

Geochemical modeling: a review

International Nuclear Information System (INIS)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted

Geochemical modeling: a review

Energy Technology Data Exchange (ETDEWEB)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted.

NOAA and MMS Marine Minerals Geochemical Database

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The Marine Minerals Geochemical Database was created by NGDC as a part of a project to construct a comprehensive computerized bibliography and geochemical database...

Novel geochemical techniques integrated in exploration for uranium deposits at depth

International Nuclear Information System (INIS)

Kyser, K.

2014-01-01

unique to uranium-rich sources. Isotopic compositions of C and N indicate microbial interactions with the uranium deposits, which is the likely process by which elements are mobilized out of the deposits and into the surrounding environment for us to use as vectors to ore. Correlations among pathfinder elements occur in fractures in core, but also in various surface media. Multi-element analyses including Pb isotopes of the clay-sized fractions of all soil horizons and vegetation provide compelling evidence that a robust geochemical signature exists. All of the processes that operate to produce geochemical anomalies at the surface above unconformity-related deposits are applicable to all other types of uranium deposits and should be integrated into learning curves for effective exploration of uranium. (author)

Use of partial dissolution techniques in geochemical exploration

Science.gov (United States)

Chao, T.T.

1984-01-01

Application of partial dissolution techniques to geochemical exploration has advanced from an early empirical approach to an approach based on sound geochemical principles. This advance assures a prominent future position for the use of these techniques in geochemical exploration for concealed mineral deposits. Partial dissolution techniques are classified as single dissolution or sequential multiple dissolution depending on the number of steps taken in the procedure, or as "nonselective" extraction and as "selective" extraction in terms of the relative specificity of the extraction. The choice of dissolution techniques for use in geochemical exploration is dictated by the geology of the area, the type and degree of weathering, and the expected chemical forms of the ore and of the pathfinding elements. Case histories have illustrated many instances where partial dissolution techniques exhibit advantages over conventional methods of chemical analysis used in geochemical exploration. ?? 1984.

Geochemical Data Package for Performance Assessment Calculations Related to the Savannah River Site

Energy Technology Data Exchange (ETDEWEB)

Kaplan, Daniel I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-07-22

The Savannah River Site (SRS) disposes of low-level radioactive waste (LLW) and stabilizes high-level radioactive waste (HLW) tanks in the subsurface environment. Calculations used to establish the radiological limits of these facilities are referred to as Performance Assessments (PA), Special Analyses (SA), and Composite Analyses (CA). The objective of this document is to revise existing geochemical input values used for these calculations. This work builds on earlier compilations of geochemical data (2007, 2010), referred to a geochemical data packages. This work is being conducted as part of the on-going maintenance program of the SRS PA programs that periodically updates calculations and data packages when new information becomes available. Because application of values without full understanding of their original purpose may lead to misuse, this document also provides the geochemical conceptual model, the approach used for selecting the values, the justification for selecting data, and the assumptions made to assure that the conceptual and numerical geochemical models are reasonably conservative (i.e., bias the recommended input values to reflect conditions that will tend to predict the maximum risk to the hypothetical recipient). This document provides 1088 input parameters for geochemical parameters describing transport processes for 64 elements (>740 radioisotopes) potentially occurring within eight subsurface disposal or tank closure areas: Slit Trenches (ST), Engineered Trenches (ET), Low Activity Waste Vault (LAWV), Intermediate Level (ILV) Vaults, Naval Reactor Component Disposal Areas (NRCDA), Components-in-Grout (CIG) Trenches, Saltstone Facility, and Closed Liquid Waste Tanks. The geochemical parameters described here are the distribution coefficient, Kd value, apparent solubility concentration, k_s value, and the cementitious leachate impact factor.

Evaluation of disposal site geochemical performance using a containment factor

International Nuclear Information System (INIS)

Lerman, A.; Domenico, P.A.; Bartlett, J.W.

1988-01-01

The containment factor is a measure of retention by geologic setting of wastes released from a repository. The factor is alternatively defined either in terms of several measurable hydrological and geochemical parameters, or in terms of amounts of waste components that may be released to the geologic setting and, subsequently, to the environment. Containment factors for individual waste components in a given geologic setting are functions of groundwater to rock volume ratios, sorption or exchange characteristics of the rocks, and containment time to groundwater travel time ratios. For high-level radioactive wastes, containment factors based on the NRC and EPA limit values for cumulative releases from waste and to the environment provide a measure of the geochemical performance of the geologic setting in tuff, basalt, and salt. The containment factor values for individual nuclides from high-level wastes indicate that for some of the nuclides containment may be achieved by groundwater travel time along. For other nuclides, additional performance functions need to be allocated to geochemical retention by such processes as sorption, ion-exchange or precipitation

Geochemical and mineralogical characteristics of Lithomargic clay

African Journals Online (AJOL)

Administrator

Geochemical and mineralogical characteristics of Lithomargic clay. GEOCHEMICAL AND .... tries, as filling material in the pulp and paper, toothpaste and paint industries as well ..... tions very vital to human health and other ac- tivities of man.

Geochemical evaluation of the near-field for future HLW repository at Olkiluoto

International Nuclear Information System (INIS)

Idiart, A.; Maia, F.; Arcos, D.

2013-10-01

The concept for the final disposal of spent nuclear fuel in Finland considers an engineered and natural (crystalline rock) multi-barrier system surrounding the spent fuel. This work aims at predicting and making a quantitative assessment of the geochemical evolution of the near-field (canister, buffer, backfill and adjacent fractured bedrock) during the unsaturated thermal period and in the long-term, after saturation has been completed. The groundwater/bentonite buffer interaction during the unsaturated thermal period is tackled through a two-dimensional (2D) axisymmetric scheme using the thermo-hydro-geochemical code TOUGHREACT. In turn, the long-term interaction of the fully water-saturated buffer and backfill with groundwater is assessed through 3D numerical models using the reactive transport code PHAST under isothermal conditions. A set of base cases have been set up based on the most plausible set of input data. In addition, a limited number of sensitivity cases have been conducted to analyse the influence of key parameters controlling the system and reduce uncertainty. Predicted mineralogical changes of accessory minerals in the bentonite for the thermal period are controlled by the dependence of mineral solubilities on temperature and on the solute transport by advection during the saturation process, and diffusion during the whole period. The results of the thermal period indicate that a small amount of the primary amorphous silica is redistributed in the buffer: dissolution close to the canister and precipitation close to the buffer - rock interface. Primary calcite dissolution/precipitation is minimal, remaining stable throughout the simulation time in all cases. Anhydrite precipitates near the canister due to the elevated temperature, while it dissolves from the outside of the buffer. The results indicate that there is no significant evaporation of water near the copper canister and thus no chloride salt reaches saturation. The geochemical changes of

Geochemical factors affecting radionuclide transport through near and far fields at a Low-Level Waste Disposal Site

International Nuclear Information System (INIS)

Kaplan, D.I.; Seme, R.J.; Piepkho, M.G.

1995-03-01

The concentration of low-level waste (LLW) contaminants in groundwater is determined by the amount of contaminant present in the solid waste, rate of release from the waste and surrounding barriers, and a number of geochemical processes including adsorption, desorption, diffusion, precipitation, and dissolution. To accurately predict radionuclide transport through the subsurface, it is essential that the important geochemical processes affecting radionuclide transport be identified and, perhaps more importantly, accurately quantified and described in a mathematically defensible manner

Geochemical Processes Data Package for the Vadose Zone in the Single-Shell Tank Waste Management Areas at the Hanford Site

Energy Technology Data Exchange (ETDEWEB)

Cantrell, Kirk J.; Zachara, John M.; Dresel, P. Evan; Krupka, Kenneth M.; Serne, R. Jeffrey

2007-09-28

This data package discusses the geochemistry of vadose zone sediments beneath the single-shell tank farms at the U.S. Department of Energy’s (DOE’s) Hanford Site. The purpose of the report is to provide a review of the most recent and relevant geochemical process information available for the vadose zone beneath the single-shell tank farms and the Integrated Disposal Facility. Two companion reports to this one were recently published which discuss the geology of the farms (Reidel and Chamness 2007) and groundwater flow and contamination beneath the farms (Horton 2007).

Proceedings of 13. International Geochemical Exploration Symposium. 2. Brazilian Geochemical Congress

International Nuclear Information System (INIS)

1989-01-01

Some works about geochemistry are presented, including themes about geochemical exploration, lithogeochemistry and isotope geochemistry, environmental geochemistry, analyical geochemistry, geochemistry of carbonatites and rare earth elements and organic geochemistry. (C.G.C.) [pt

The geochemical atlas of Alaska, 2016

Science.gov (United States)

Lee, Gregory K.; Yager, Douglas B.; Mauk, Jeffrey L.; Granitto, Matthew; Denning, Paul; Wang, Bronwen; Werdon, Melanie B.

2016-06-21

A rich legacy of geochemical data produced since the early 1960s covers the great expanse of Alaska; careful treatment of such data may provide significant and revealing geochemical maps that may be used for landscape geochemistry, mineral resource exploration, and geoenvironmental investigations over large areas. To maximize the spatial density and extent of data coverage for statewide mapping of element distributions, we compiled and integrated analyses of more than 175,000 sediment and soil samples from three major, separate sources: the U.S. Geological Survey, the National Uranium Resource Evaluation program, and the Alaska Division of Geological & Geophysical Surveys geochemical databases. Various types of heterogeneity and deficiencies in these data presented major challenges to our development of coherently integrated datasets for modeling and mapping of element distributions. Researchers from many different organizations and disparate scientific studies collected samples that were analyzed using highly variable methods throughout a time period of more than 50 years, during which many changes in analytical techniques were developed and applied. Despite these challenges, the U.S. Geological Survey has produced a new systematically integrated compilation of sediment and soil geochemical data with an average sample site density of approximately 1 locality per 10 square kilometers (km2) for the entire State of Alaska, although density varies considerably among different areas. From that compilation, we have modeled and mapped the distributions of 68 elements, thus creating an updated geochemical atlas for the State.

Geochemical tracing and hydrogeochemical modelling of water-rock interactions during salinization of alluvial groundwater (Upper Rhine Valley, France)

Energy Technology Data Exchange (ETDEWEB)

Lucas, Y., E-mail: yann.lucas@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Schmitt, A.D., E-mail: anne-desiree.schmitt@univ-fcomte.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)] [Universite de Franche-Comte et CNRS-UMR 6249, Chrono-Environnement, 16, Route de Gray, 25030 Besancon Cedex (France); Chabaux, F., E-mail: francois.chabaux@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Clement, A.; Fritz, B. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Elsass, Ph. [BRGM, GEODERIS, 1, rue Claude Chappe, 57070 Metz (France); Durand, S. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)

2010-11-15

Research highlights: {yields} Major and trace elements along with strontium and uranium isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect a conservative mixing. {yields} A coupled hydrogeochemical model demonstrates that cationic exchange between alkalis from polluted waters and alkaline-earth elements from montmorillonite present in the host rock of the aquifer is the primary process. {yields} The model requires only a small amount of montmorillonite. {yields} It is necessary to consider the pollution history to explain the important chloride, sodium and calcium concentration modifications. {yields} The model shows that the rapidity of the cationic exchange reactions insures a reversibility of the cation fixation on clays in the aquifer. - Abstract: In the southern Upper Rhine Valley, groundwater has undergone intensive saline pollution caused by the infiltration of mining brines, a consequence of potash extraction carried out during the 20th century. Major and trace elements along with Sr and U isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect conservative mixing between saline waters resulting from the dissolution of waste heaps and one or more unpolluted end-members. The results imply the occurrence of interactions between host rocks and polluted waters, and they suggest that cationic exchange mechanisms are the primary controlling process. A coupled hydrogeochemical model has been developed with the numerical code KIRMAT, which demonstrates that cationic exchange between alkalis from polluted waters and alkaline-earth elements from montmorillonite present in the host rock of the aquifer is the primary process controlling the geochemical evolution of the groundwater. The model requires only a small amount of montmorillonite (between 0.75% and 2.25%), which is in agreement with the observed mineralogical composition of the aquifer. The model also proves

Geochemical controls on the composition of soil pore waters beneath a mixed waste disposal site in the unsaturated zone

International Nuclear Information System (INIS)

Rawson, S.A.; Hubbell, J.M.

1989-01-01

Soil pore waters are collected routinely to monitor a thick unsaturated zone that separates a mixed waste disposal site containing transuranic and low-level radioactive wastes from the Snake River Plain aquifer. The chemistry of the soil pore waters has been studied to evaluate the possible control on the water composition by mineral equilibria and determine the extent, if any, of migration of radionuclides from the disposal site. Geochemical codes were used to perform speciation calculations for the waters. The results of speciation calculations suggest that the installation of the lysimeters affects the observed silica contents of the soil pore waters. The results also establish those chemical parameters that are controlled by secondary mineral precipitation. 15 refs., 6 figs., 1 tab

Geochemical approach to evaluate deforest of mangroves

OpenAIRE

Ishiga, Hiroaki; Diallo, Ibrahima M'bemba; Bah Mamadou Lamine Malick,; Ngulimi. Faustine Miguta,; Magai. Paschal Justin,; Shati Samwel Stanley,

2016-01-01

Processes of mangrove deforest related human activities were examined. To evaluate changes of soil feature, multielements geochemical compositions of mangrove muds and soils of deforest were analyzed. To describe present situation of the mangrove, Conakry in Guinea, Dar es Salaam in Tanzania, Sundarbans of Bangladesh and Nago in Okinawa of Japan were selected. Soil samples of the forests were evaluated enrichment of biologically concentrated heavy metals such as Zn, Cu and Fe, and TS (total s...

Geochemical signature of radioactive waste: oil NORM

International Nuclear Information System (INIS)

Costa, Gilberto T. de Paula; Costa-de-Moura, Jorge; Gomes, Carlos de Almeida; Sampaio, Emidio A. Lopes

2017-01-01

The Brazilian Nuclear Agency (CNEN) rules all nuclear activity in Brazil as demanded by the Federal Constitution, articles 21, XXIII, and 177, V, and by the Federal Acts 4.118/62 and 10.308/2001. Therefore, the CNEN is responsible for any radioactive waste disposal in the country. Oil Naturally Occurring Radioactive Materials (Oil NORM) in this paper refers to waste coming from oil exploration. Oil NORM has called much attention during the last decades, mostly because it is not possible to determine its primary source due to the actual absence of regulatory control mechanism. There is no efficient regulatory tool which allows determining the origin of such NORM wastes even among those facilities under regulatory control. This fact may encourage non-authorized radioactive material transportation, smuggling and terrorism. The aim of this project is to provide a geochemical signature for each oil NORM waste using its naturally occurring isotopic composition to identify its origin. The here proposed method is a specific geochemical modeling of oil sludge NORM samples which are analyzed for radioisotopes normally present in oil pipes, such as 228 Ac, 214 Bi and 214 Pb. The activity ratios are plotted in scatter diagrams. This method was successfully tested with data of different sources obtained from analysis reports from the Campos Basin/Brazil and from literature. (author)

Geochemical signature of radioactive waste: oil NORM

Energy Technology Data Exchange (ETDEWEB)

Costa, Gilberto T. de Paula; Costa-de-Moura, Jorge; Gomes, Carlos de Almeida; Sampaio, Emidio A. Lopes, E-mail: gilberto.costa@cnen.gov.br, E-mail: jcmoura@cnen.gov.br, E-mail: cgomes@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN), Rio de Janeiro, RJ (Brazil). Div. de Controle de Rejeitos e Transporte de Materiais Radioativos

2017-07-01

The Brazilian Nuclear Agency (CNEN) rules all nuclear activity in Brazil as demanded by the Federal Constitution, articles 21, XXIII, and 177, V, and by the Federal Acts 4.118/62 and 10.308/2001. Therefore, the CNEN is responsible for any radioactive waste disposal in the country. Oil Naturally Occurring Radioactive Materials (Oil NORM) in this paper refers to waste coming from oil exploration. Oil NORM has called much attention during the last decades, mostly because it is not possible to determine its primary source due to the actual absence of regulatory control mechanism. There is no efficient regulatory tool which allows determining the origin of such NORM wastes even among those facilities under regulatory control. This fact may encourage non-authorized radioactive material transportation, smuggling and terrorism. The aim of this project is to provide a geochemical signature for each oil NORM waste using its naturally occurring isotopic composition to identify its origin. The here proposed method is a specific geochemical modeling of oil sludge NORM samples which are analyzed for radioisotopes normally present in oil pipes, such as {sup 228}Ac, {sup 214}Bi and {sup 214}Pb. The activity ratios are plotted in scatter diagrams. This method was successfully tested with data of different sources obtained from analysis reports from the Campos Basin/Brazil and from literature. (author)

The IUGS/IAGC Task Group on Global Geochemical Baselines

Science.gov (United States)

Smith, David B.; Wang, Xueqiu; Reeder, Shaun; Demetriades, Alecos

2012-01-01

The Task Group on Global Geochemical Baselines, operating under the auspices of both the International Union of Geological Sciences (IUGS) and the International Association of Geochemistry (IAGC), has the long-term goal of establishing a global geochemical database to document the concentration and distribution of chemical elements in the Earth’s surface or near-surface environment. The database and accompanying element distribution maps represent a geochemical baseline against which future human-induced or natural changes to the chemistry of the land surface may be recognized and quantified. In order to accomplish this long-term goal, the activities of the Task Group include: (1) developing partnerships with countries conducting broad-scale geochemical mapping studies; (2) providing consultation and training in the form of workshops and short courses; (3) organizing periodic international symposia to foster communication among the geochemical mapping community; (4) developing criteria for certifying those projects whose data are acceptable in a global geochemical database; (5) acting as a repository for data collected by those projects meeting the criteria for standardization; (6) preparing complete metadata for the certified projects; and (7) preparing, ultimately, a global geochemical database. This paper summarizes the history and accomplishments of the Task Group since its first predecessor project was established in 1988.

A Spatially Constrained Multi-autoencoder Approach for Multivariate Geochemical Anomaly Recognition

Science.gov (United States)

Lirong, C.; Qingfeng, G.; Renguang, Z.; Yihui, X.

2017-12-01

Separating and recognizing geochemical anomalies from the geochemical background is one of the key tasks in geochemical exploration. Many methods have been developed, such as calculating the mean ±2 standard deviation, and fractal/multifractal models. In recent years, deep autoencoder, a deep learning approach, have been used for multivariate geochemical anomaly recognition. While being able to deal with the non-normal distributions of geochemical concentrations and the non-linear relationships among them, this self-supervised learning method does not take into account the spatial heterogeneity of geochemical background and the uncertainty induced by the randomly initialized weights of neurons, leading to ineffective recognition of weak anomalies. In this paper, we introduce a spatially constrained multi-autoencoder (SCMA) approach for multivariate geochemical anomaly recognition, which includes two steps: spatial partitioning and anomaly score computation. The first step divides the study area into multiple sub-regions to segregate the geochemical background, by grouping the geochemical samples through K-means clustering, spatial filtering, and spatial constraining rules. In the second step, for each sub-region, a group of autoencoder neural networks are constructed with an identical structure but different initial weights on neurons. Each autoencoder is trained using the geochemical samples within the corresponding sub-region to learn the sub-regional geochemical background. The best autoencoder of a group is chosen as the final model for the corresponding sub-region. The anomaly score at each location can then be calculated as the euclidean distance between the observed concentrations and reconstructed concentrations of geochemical elements.The experiments using the geochemical data and Fe deposits in the southwestern Fujian province of China showed that our SCMA approach greatly improved the recognition of weak anomalies, achieving the AUC of 0.89, compared

Reconnaissance Geochemical Study

African Journals Online (AJOL)

distribution patterns. The geochemical distribution maps of the elements reveal that Cu, Pb, Zn, Co, Sc, Ni, Cr, .... After filtration, the leached solutions were diluted with ultra ...... some other rare earth elements in the study area. The occurrence ...

Geochemical evolution of highly alkaline and saline tank waste plumes during seepage through vadose zone sediments

International Nuclear Information System (INIS)

Wan, Jiamin; Tokunaga, Tetsu K.; Larsen, Joern T.; Serne, R. JEFFREY

2004-01-01

Leakage of highly saline and alkaline radioactive waste from storage tanks into underlying sediments is a serious environmental problem at the Hanford Site in Washington State. This study focuses on geochemical evolution of tank waste plumes resulting from interactions between the waste solution and sediment. A synthetic tank waste solution was infused into unsaturated Hanford sediment columns (0.2, 0.6, and 2 m) maintained at 70C to simulate the field contamination process. Spatially and temporally resolved geochemical profiles of the waste plume were obtained. Thorough OH neutralization (from an initial pH 14 down to 6.3) was observed. Three broad zones of pore solutions were identified to categorize the dominant geochemical reactions: the silicate dissolution zone (pH > 10), pH-neutralized zone (pH 10 to 6.5), and displaced native sediment pore water (pH 6.5 to 8). Elevated concentrations of Si, Fe, and K in plume fluids and their depleted concentrations in plume sediments reflected dissolution of primary minerals within the silicate dissolution zone. The very high Na concentrations in the waste solution resulted in rapid and complete cation exchange, reflected in high concentrations of Ca and Mg at the plume front. The plume-sediment profiles also showed deposition of hydrated solids and carbonates. Fair correspondence was obtained between these results and analyses of field borehole samples from a waste plume at the Hanford Site. Results of this study provide a well-defined framework for understanding waste plumes in the more complex field setting and for understanding geochemical factors controlling transport of contaminant species carried in waste solutions that leaked from single-shell storage tanks in the past

Development of thermodynamic databases and geochemical/transport models for prediction of long-term radionuclide migration (Germany)

International Nuclear Information System (INIS)

Kienzler, B.

2000-01-01

The isolation capacity of a repository system for radionuclides is described by geochemical modeling. The models for interpretation of experimental findings and for long-term extrapolation of experimental results are based on thermodynamic approaches. The geochemical models include dissolution reactions of waste forms, the evolution of the geochemical milieu, interactions of radionuclides with constituents of the groundwater (brines) and the precipitation of new solid phases. Reliable thermodynamic data, understanding of radionuclide complexation in aqueous multi-electrolyte solutions at the relevant ionic strength and knowledge on the formation of pure and mixed solids and on sorption processes are urgently needed for such model calculations. (author)

Geochemical processes in acidic water caused by the weathering of metal sulphides; Procesos geoquimicos en aguas acidas por meteorizacion de sulfuros

Energy Technology Data Exchange (ETDEWEB)

Asta Andres, M. P.; Acero Salazar, P.; Auque Sanz, L. F.; Gimeno Serrano, M. J.; Gomez Jimenez, J. B.

2011-07-01

Acid generated by the oxidative dissolution of metal sulphides is one of the main sources of pollution in runoff water, groundwater, soils and sediments throughout the world. These types of water are very acidic and contain high concentrations of sulphate and other potentially contaminating elements such Fe, As, Cd, Sb, Zn and Cu. The acidity generated by sulphide oxidation processes is mainly controlled by the type, quantity and distribution of the sulphide-rich rocks, by the physical characteristics of the rocks (since they determine the accessibility of aqueous solutions and gases to the sulphides), by the presence of microorganisms able to catalyze the main chemical reactions involved in the formation of acid drainage, and by the existence of minerals capable of neutralizing acidity. As a result, the generation of acidic water is a very complex problem, the study of which must be undertaken via a multidisciplinary approach, taking into account geological, geochemical, mineralogical and microbiological aspects among others. The aim of our work is to provide a general overview of these processes and other factors that influence the generation and evolution of these systems, together with information concerning current scientific knowledge about each of these approaches. Thus we hope to provide a basic background to the understanding and study of acid-water systems associated with the weathering of metal sulphides and the processes involved in the generation, migration, evolution and natural attenuation of acidic waters in these environments. (Author) 65 refs.

The chemical evolution of a travertine-depositing stream: Geochemical processes and mass transfer reactions

Science.gov (United States)

Lorah, Michelle M.; Herman, Janet S.

1988-01-01

This field study focuses on quantitatively defining the chemical changes occurring in Falling Spring Creek, a travertine-depositing stream located in Alleghany County, Virginia. The processes of CO2outgassing and calcite precipitation or dissolution control the chemical evolution of the stream. The observed chemical composition of the water was used with the computerized geochemical model WATEQF to calculate aqueous speciation, saturation indices, and CO2 partial pressure values. Mass balance calculations were performed to obtain mass transfers of CO2 and calcite. Reaction times, estimated from stream discharge, were used with the mass transfer results to calculate rates of CO2, outgassing and calcite precipitation between consecutive sampling points. The stream, which is fed by a carbonate spring, is supersaturated with respect to CO2 along the entire 5.2-km flow path. Outgassing of CO2 drives the solution to high degrees of supersaturation with respect to calcite. Metabolic uptake of CO2 by photosynthetic plants is insignificant, because the high supply rate of dissolved carbon dioxide and the extreme agitation of the stream at waterfalls and rapids causes a much greater amount of inorganic CO2 outgassing to occur. Calcite precipitation is kinetically inhibited until near the crest of a 20-m vertical waterfall. Calcite precipitation rates then reach a maximum at the waterfall where greater water turbulence allows the most rapid escape of CO2. Physical evidence for calcite precipitation exists in the travertine deposits which are first observed immediately above the waterfall and extend for at least 1.0 km below the falls. Net calcite precipitation occurs at all times of the year but is greatest during low-flow conditions in the summer and early fall.

Coupling of transport and geochemical models

International Nuclear Information System (INIS)

Noy, D.J.

1986-01-01

This report considers mass transport in the far-field of a radioactive waste repository, and detailed geochemical modelling of the ground-water in the near-field. A parallel approach to this problem of coupling transport and geochemical codes is the subject of another CEC report (ref. EUR 10226). Both studies were carried out in the framework of the CEC project MIRAGE. (Migration of radionuclides in the geosphere)

Biological and geochemical processes involved during denitrification in Callovo-Oxfordian clay

International Nuclear Information System (INIS)

Ollivier, P.; Parmentier, M.; Joulian, C.; Pauwels, H.; Albrecht, A.

2012-01-01

Document available in extended abstract form only. The clay-rich Callovo-Oxfordian (COx) formation has been selected for the disposal of medium and high level, long-lived radioactive waste. After waste cell closure and degradation of package some intermediate-level waste will release nitrate. The latter is likely to diffuse into the surrounding environment (engineered barriers and geological host formation) and interact with a variety compounds present in the barrier components and the rocks. These interactions may result in modification of chemical conditions and impact storage conditions and radionuclide retention. Our work is focused on the understanding of the fate of nitrates released during and after degradation of waste package. We developed a coupled approach considering both geochemical and biological processes of nitrate reduction to simulate reactions occurring at the interface of the engineered barrier and the clay-rich COx formation. Laboratory experiments have been carried out in order to acquire data on kinetics of denitrification coupled with a molecular approach using enzymatic and metabolic activities as a tool for an accurate estimation of biomass. Denitrification has been monitored in a synthetic solution comparable to COx pore water supplemented with acetate and nitrate and amended with a heterotrophic denitrifying strain, Pseudomonas mandelii. Several conditions are applied considering different acetate/nitrate ratios in the presence or absence of COx clay. Before the beginning of experiments, the headspace is flushed with N 2 gas to remove oxygen from flasks. Acetylene is used to stop denitrification reaction after the production of N 2 O gas and thus avoid the formation of N 2 gas. Two successive redox reactions are thus expected to occur in experiments. Samples are regularly collected to analyze physical and chemical parameters as well as biological parameters. Biomass is estimated and monitored using both optical microscopy and

Concerning evaluation of eco-geochemical background in remediation strategy

Science.gov (United States)

Korobova, Elena; Romanov, Sergey

2015-04-01

The geochemical concept of biosphere developed by V.I. Vernadsky states the geological role of the living organisms in the course of their active chemical interaction with the inert matter (Vernadsky, 1926, 1960). Basing on this theory it is reasonable to suggest that coevolution of living organisms and their environment led to development of the dynamically stable biogeocenoses precisely adequate to their geochemical environment. Soil cover was treated by V.I. Vernadsky as a balanced bio-inert matter resulting from this interaction. Appearance of human mind and then a civilization led to global expansion of human beings, first able to survive in unfavorable geochemical conditions and then starting chemical transformation of the environment to satisfy the growing demands of mankind in food and energy. The residence in unfavorable environment and local contamination was followed by appearance of endemic diseases of plants, animals and man. Therefore zonal, regional and local chemical composition of the soil cover formed in natural conditions may be used for estimation of the optimum geochemical background, most adequate for the corresponding zonal biogeocenoses and species. Moreover, the natural geochemical background and technogenic fields have unequal spatial structure and this facilitates their identification that may be relatively easy realized in remediation strategy. On the assumption of the foregoing, the adequate methodical approach to remediation of technogenically affected areas should account of the interaction of the existing natural and the newly formed technogenic geochemical fields and include the following steps: 1) the study and mapping of geochemical structure of the natural geochemical background basing on soil maps; 2) the study of contaminants and mapping spatial distribution of technogenic releases; 3) construction of risk maps for the target risk groups with due regard to natural ecological threshold concentration in context of risk degree for

Geochemical modelling of groundwater evolution and residence time at the Haestholmen site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy, Helsinki (Finland); Leino- Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

2001-01-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the geological final disposal of radioactive waste. The performance of technical barriers and migration of possibly released radionuclides depend on the geochemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions that control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors that control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the crystalline bedrock at Haestholmen has been created and the significance of geochemical reactions and groundwater mixing along different flow paths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on water samples (64 altogether) obtained from precipitation, the Baltic Sea, the soil layer, shallow wells in the bedrock, and 14 deep boreholes in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and their isotopic measurements were also utilised. The data covers the bedrock at Haestholmen to a depth of 1000 m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used to evaluate evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution ({delta}{sup 13}C and {delta}{sup 34}S) and mixing of palaeo-water types were approached by mass-balance calculations (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The interpretation and calculation of hydrochemical data from Haestholmen suggest that changes in external conditions, such as glaciation

Geochemical mass balance for sulfur- and nitrogen-bearing acid components: Eastern United States

International Nuclear Information System (INIS)

Bischoff, W.D.; Mackenzie, F.T.; Paterson, V.L.

1984-01-01

The impact on a geographical region of SO 2 and nitrogen oxides (NO /SUB x/ ) emissions to the atmosphere because of man's activities (e.g., burning of fossil fuels and smelting of sulfide ores) usually has not been considered in terms of a regional geochemical mass balance model. Mass balance models, however, have been employed extensively on a global scale. The models evaluate reservoir sizes, processes and fluxes associated with the transfer of a substance within a system of interest. The models may be steady- or transient-state, and include assessment of historical (geologic), present and future data and processes. In this chapter a geochemical mass balance model is applied to constituents of acid precipitation (H + , NO - 3 and SO 2- ) to evaluate the impact of acid precipitation on the eastern United States

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy, Helsinki (Finland); Leino-Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

1998-12-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the bedrock at Kivetty has been created and the significance of chemical reactions along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on groundwater samples (38 altogether) obtained from the soil layer, shallow wells in the bedrock, and five deep multi-packered boreholes (KRI-KR5) in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and their isotopic measurements were also utilised. The data covers the bedrock at Kivetty to a depth of 850m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and C-14 age calculations of groundwater was given a mass-balance approach (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The hydrogeochemistry of Kivetty is characterised by evolution from low-saline-carbonate-rich recharge water towards Na-Ca-Cl-type water. The salinity remains low. The most important changes in the chemistry of the

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

International Nuclear Information System (INIS)

Pitkaenen, P.; Luukkonen, A.; Ruotsalainen, P.; Leino-Forsman, H.; Vuorinen, U.

1998-12-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the bedrock at Kivetty has been created and the significance of chemical reactions along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on groundwater samples (38 altogether) obtained from the soil layer, shallow wells in the bedrock, and five deep multi-packered boreholes (KRI-KR5) in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and their isotopic measurements were also utilised. The data covers the bedrock at Kivetty to a depth of 850m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and C-14 age calculations of groundwater was given a mass-balance approach (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The hydrogeochemistry of Kivetty is characterised by evolution from low-saline-carbonate-rich recharge water towards Na-Ca-Cl-type water. The salinity remains low. The most important changes in the chemistry of the

Modelling of leaching and geochemical processes in an aged MSWIBA subbase layer

Energy Technology Data Exchange (ETDEWEB)

Bendz, David; Suer, Pascal; Sloot, Hans van der; Kosson, David; Flyhammar, Peter

2009-07-15

In a previous project, the accumulated effects of leaching and aging in a subbase layer of bottom ash in a test road were investigated. The test road were constructed in 1987 in Linkoeping, Sweden, and was in use until the start of the Vaendoera Q4-241 study in September 2003. The overall objective of the present study is to bring the evaluation of the previous project (Q4-241) further by taking advantage of the existing data, perform complementary laboratory experiments on four composite samples reflecting different degree of exposure to atmosphere and leaching. The specific objectives were to investigate: (i) what processes and mineral phases that govern leaching of macro- and trace elements and DOC in the bottom ash after 16 years (1987- 2003) of aging under field conditions. (ii) how the hydrologic conditions, infiltration of water and leachate production has evolved with time. The following tests were performed on the composite samples: pH-stat test, column test, Fe/Al oxide extraction and TOC fractioning. Geochemical and hydrological modelling where performed with LeachXS/Orchestra and Hydrus 2-D. Daily precipitation data from the Swedish Meteorological and Hydrological Institute (SMHI) from the Malmslaett (Linkoeping) measurement station was used in the hydrological modelling of January 1988 to the 1st of september 2003. The hydraulic modeling results show that the bottom ash subbase layer endure seasonal wet and dry cycles. The results confirm that, depending on the boundary conditions along the shoulders the capillary potential may drive moisture either in or out of the road body. The water retention parameters for bottom ash were crucial in the hydraulic modeling and the capillary forces in bottom ash were found to be significant with a water retention curve close to silt. This explains the observed depletion of easily soluble salts in the test road. The results showed that the accumulated LS ratio for the bottom ash subbase layer reached about LS:10 in

Geochemical factors in borehole-shaft plug longevity

International Nuclear Information System (INIS)

Roy, D.M.

1981-01-01

Geochemical investigations that address factors controlling the longevity of repository sealing materials in a geochemical environment are discussed. Studies are being made of cement-based materials as major candidates for seals for borehole plugging, and shaft and tunnel sealing in certain potential repository environments. Factors controlling the extent of attainment of equilibrium of the plug components with time and the rate of approach to a state of stable equilibrium of the plug component chemical subsystem within the total system are discussed. The effect of these factors on changes in physical, mechanical and thermal properties of a seal system, and the consequent effectiveness of the seal in preventing transport of radioactive waste species are the dominant features to be determined. Laboratory experiments on the effects of anticipated temperature, pressure, and environmental factors (including chemical composition and specific rock type) are described. Thermodynamic studies are used to determine the potentially stable reaction products under conditions similar to those anticipated for the repository boreholes, shafts, and tunnels during and after the operating stage. Multitemperature reaction series are studied, and reaction kinetics are investigated for the purpose of predicting the course of likely reactions. Detailed studies of permeability, diffusion, and interfacial properties and chemical and microphase characterization of the products of experiments are carried out. Characterization studies of old and ancient cements, mortars, and concretes and prototype man-made seal materials are performed to further assess the factors associated with longevity

Geochemical Investigations of Groundwater Stability

International Nuclear Information System (INIS)

Bath, Adrian

2006-05-01

The report describes geochemical parameters and methods that provide information about the hydrodynamic stability of groundwaters in low permeability fractured rocks that are potential hosts for radioactive waste repositories. Hydrodynamic stability describes the propensity for changes in groundwater flows over long timescales, in terms of flow rates and flow directions. Hydrodynamic changes may also cause changes in water compositions, but the related issue of geochemical stability of a potential repository host rock system is outside the scope of this report. The main approaches to assessing groundwater stability are numerical modelling, measurement and interpretation of geochemical indicators in groundwater compositions, and analyses and interpretations of secondary minerals and fluid inclusions in these minerals. This report covers the latter two topics, with emphasis on geochemical indicators. The extent to which palaeohydrogeology and geochemical stability indicators have been used in past safety cases is reviewed. It has been very variable, both in terms of the scenarios considered, the stability indicators considered and the extent to which the information was explicitly or implicitly used in assessing FEPs and scenarios in the safety cases. Geochemical indicators of hydrodynamic stability provide various categories of information that are of hydrogeological relevance. Information about groundwater mixing, flows and water sources is potentially provided by the total salinity of groundwaters, their contents of specific non-reactive solutes (principally chloride) and possibly of other solutes, the stable isotopic ratio of water, and certain characteristics of secondary minerals and fluid inclusions. Information pertaining directly to groundwater ages and the timing of water and solute movements is provided by isotopic systems including tritium, carbon-14, chlorine-36, stable oxygen and hydrogen isotopes, uranium isotopes and dissolved mobile gases in

Quantitative study of Portland cement hydration by X-Ray diffraction/Rietveld analysis and geochemical modeling

Science.gov (United States)

Coutelot, F.; Seaman, J. C.; Simner, S.

2017-12-01

In this study the hydration of Portland cements containing blast-furnace slag and type V fly ash were investigated during cement curing using X-ray diffraction, with geochemical modeling used to calculate the total volume of hydrates. The goal was to evaluate the relationship between the starting component levels and the hydrate assemblages that develop during the curing process. Blast furnace-slag levels of 60, 45 and 30 wt.% were studied in blends containing fly ash and Portland cement. Geochemical modelling described the dissolution of the clinker, and predicted quantitatively the amount of hydrates. In all cases the experiments showed the presence of C-S-H, portlandite and ettringite. The quantities of ettringite, portlandite and the amorphous phases as determined by XRD agreed well with the calculated amounts of these phases after different periods of time. These findings show that changes in the bulk composition of hydrating cements can be described by geochemical models. Such a comparison between experimental and modelled data helps to understand in more detail the active processes occurring during cement hydration.

In situ geochemical properties of clays subject to thermal loading

International Nuclear Information System (INIS)

Chapman, N.A.

1980-01-01

Compositional variation and geochemical environment in an argillaceous unit are a function of age, depth of burial and mode of origin. This paper considers the variation limits likely to be encountered in potential repository host rocks and examines the significance of factors such as porosity, pore-fluid pressure, total fluid content, and major and accessory mineral component behaviors in controlling the geochemical environment in the neighbourhood of a thermally active waste canister. Particular attention is paid to the use of Eh-pH diagrams in assessing corrosion environments and nuclide speciation. The paper outlines the variables which must be considered when endeavouring to interpret such plots (e.g. temperature, concentration, concurrent reactions and probabilities) and uses the behavior of various iron minerals found in clay deposits under specific conditions to illustrate the complexities. The overall thermal stability of various clay and accessory minerals is discussed and extended to attempt to predict behavior under deep repository conditions, using available data on the diagenetic characteristics of clay-rich sediments. The physical behavior of fluids in plastic clays is considered and methods evaluated for deriving induced geochemical conditions in a thermally active repository. The latter section is particularly related to canister corrosion studies, in situ experiments, and waste dissolution parameters

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Tonsina area, Valdez Quadrangle, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 128 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Tonsina area in the Chugach Mountains, Valdez quadrangle, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated into the statewide geochemical databases of both agencies

Application of Neutron Activation Analysis to Geochemical Studies of Mineral Resources

Energy Technology Data Exchange (ETDEWEB)

Winchester, J. W. [Department Of Meteorology and Oceanography, University of Michigan, Ann Arbor, MI (United States); Catoggio, J. A. [Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata (Argentina)

1969-03-15

Sensitive and accurate measurement of closely related trace element concentrations in naturally occurring materials leads to the most useful geochemical information in the study of crystallizing systems. Studies of the rare earth elements have shown regularities that can be related to geological crystallization processes in igneous and sedimentary materials, and it is likely that similar studies of economic mineral deposits will lead to similar information. An analytical method should be chosen with great care to assure adequate sensitivity for the trace elements under investigation. Neutron activation analysis and spark source mass spectrometry both have high sensitivity adequate for many geochemical applications. However, simpler methods, such as atomic absorption, absorption spectrophotometry and electrochemical methods have adequate sensitivity for many elements and are preferred when suitable. (author)

Geochemical and geologic factors effecting the formulation of gas hydrate: Task No. 5, Final report

Energy Technology Data Exchange (ETDEWEB)

Kvenvolden, K.A.; Claypool, G.E.

1988-01-01

The main objective of our work has been to determine the primary geochemical and geological factors controlling gas hydrate information and occurrence and particularly in the factors responsible for the generation and accumulation of methane in oceanic gas hydrates. In order to understand the interrelation of geochemical/geological factors controlling gas hydrate occurrence, we have undertaken a multicomponent program which has included (1) comparison of available information at sites where gas hydrates have been observed through drilling by the Deep Sea Drilling Project (DSDP) on the Blake Outer Ridge and Middle America Trench; (2) regional synthesis of information related to gas hydrate occurrences of the Middle America Trench; (3) development of a model for the occurrence of a massive gas hydrate as DSDP Site 570; (4) a global synthesis of gas hydrate occurrences; and (5) development of a predictive model for gas hydrate occurrence in oceanic sediment. The first three components of this program were treated as part of a 1985 Department of Energy Peer Review. The present report considers the last two components and presents information on the worldwide occurrence of gas hydrates with particular emphasis on the Circum-Pacific and Arctic basins. A model is developed to account for the occurrence of oceanic gas hydrates in which the source of the methane is from microbial processes. 101 refs., 17 figs., 6 tabs.

Coupling between a geochemical model and a transport model of dissolved elements

International Nuclear Information System (INIS)

Jacquier, P.

1988-10-01

In order to assess the safety analysis of an underground repository, the transport of radioelements in groundwater and their interactions with the geological medium are modelled. The objective of this work is the setting up and experimental validation of the coupling of a geochemical model with a transport model of dissolved elements. A laboratory experiment was developed at the CEA center of Cadarache. Flow-through experiments were carried out on columns filled with crushed limestone, where several inflow conditions were taken into account as the temperature, the presence of a pollutant (strontium chloride) at different concentrations. The results consist of the evolution of the chemical composition of the water at the outlet of the column. The final aim of the study is to explain these results with a coupled model where geochemical and transport phenomena are modelled in a two-step procedure. This code, called STELE, was built by introducing a geochemical code, CHIMERE, into an existing transport code, METIS. At this stage, the code CHIMERE can take into account: any chemical reaction in aqueous phase (complexation, acid-base reaction, redox equilibrium), dissolution-precipitation of minerals and solid phases, dissolution-degassing of gas. The paper intends to describe the whole process leading to the coupling which can be forecasted over the next years between geochemical and transport models

Anthropogenic Increase Of Soil Erosion In The Gangetic Plain Revealed By Geochemical Budget Of Erosion

Science.gov (United States)

Galy, V.; France-Lanord, C.; Galy, A.; Gaillardet, J.

2007-12-01

Tectonic and climatic factors are the key natural variables controlling the erosion through complex interactions. Nonetheless, over the last few hundred years, human activity also exerts a dominant control in response to extensive land use. The geochemical budget of erosion allows the balance between the different erosion processes to be quantified. The chemical composition of river sediment results from the chemical composition of the source rock modified by (1) weathering reactions occurring during erosion and (2) physical segregation during transport. If erosion is at steady state, the difference between the chemical composition of source rocks and that of river sediments must therefore be counterbalanced by the dissolved flux. However, climatic variations or anthropic impact can induce changes in the erosion distribution in a given basin resulting in non steady state erosion. Using a mass balance approach, the comparison of detailed geochemical data on river sediments with the current flux of dissolved elements allows the steady state hypothesis to be tested. In this study, we present a geochemical budget of weathering for the Ganga basin, one of the most densely populated basin in the world, based on detailed sampling of Himalayan rivers and of the Ganga in the delta. Sampling includes depth profile in the river, to assess the variability generated by transport processes. Himalayan river sediments are described by the dilution of an aluminous component (micas + clays + feldspars) by quartz. Ganga sediments on the other hand correspond to the mixing of bedload, similar to coarse Himalayan sediments, with an aluminous component highly depleted in alkaline elements. Compared with the dissolved flux, the depletion of alkaline elements in Ganga sediments shows that the alkaline weathering budget is imbalanced. This imbalance results from an overabundance of fine soil material in the Ganga sediment relative to other less weathered material directly derived from

Report on the geological-geochemical research carried out within the area of geochemical anomaly P7, Vathyrema, Drama Department

International Nuclear Information System (INIS)

Stavropoulos, Athanasios.

1982-08-01

The investigated area covering about 30 km 2 is situated in the crystalline massive of Rhodope (north of Drama deparment, E. Macedonia) where granitoids constitute its main petrological type. The geological-geochemical and radiometric investigations carried out so far in the area have localized a large number of places with high values of γ-radiation (1.000 - 15.000 c/s), as well as high concentrations of uranium (50-500 ppm). The uranium mineralization within the zone of oxidation is expressed by the uranium mineral autunite, accompanied by intensive hematitization-limonitization and chloritization-kaolinization, and additionally by small spots and veinlets of pyrite and galena. It seems that tectonic control exists on the uranium mineralization, since most of the anomalous concentrations of uranium are sitting along mylonite zones rich in chlorite and kaolin. There have been discerned seven more anomalous part areas which will have to be covered by geochemical stream sediment sampling (phase 3), as well as geological mapping (scale 1:5.000). The results from the research conducted within the concerned anomaly lead us to the conclusion that this area is very promising and possibilities of localization of uranium payable concentrations are very high. (N.Ch.)

Geochemical monitoring using noble gases and carbon isotopes: study of a natural reservoir

International Nuclear Information System (INIS)

Jeandel, E.

2008-12-01

To limit emissions of greenhouse gases in the atmosphere, CO 2 geological sequestration appears as a solution in the fight against climate change. The development of reliable monitoring tools to ensure the sustainability and the safety of geological storage is a prerequisite for the implementation of such sites. In this framework, a geochemical method using noble gas and carbon isotopes geochemistry has been tested on natural and industrial analogues. The study of natural analogues from different geological settings showed systematic behaviours of the geochemical parameters, depending on the containment sites, and proving the effectiveness of these tools in terms of leak detection and as tracers of the behaviour of CO 2 . Moreover, an experience of geochemical tracing on a natural gas storage has demonstrated that it is possible to identify the physical-chemical processes taking place in the reservoir to a human time scale, increasing interest in the proposed tool and providing general information on its use. (author)

Simulation of radionuclide retardation at Yucca Mountain using a stochastic mineralogical/geochemical model

International Nuclear Information System (INIS)

Birdsell, K.H.; Campbell, K.; Eggert, K.; Travis, B.J.

1990-01-01

This paper presents preliminary transport calculations for radionuclide movement at Yucca Mountain. Several different realizations of spatially distributed sorption coefficients are used to study the sensitivity of radionuclide migration. These sorption coefficients are assumed to be functions of the mineralogic assemblages of the underlying rock. The simulations were run with TRACRN 1 , a finite-difference porous flow and radionuclide transport code developed for the Yucca Mountain Project. Approximately 30,000 nodes are used to represent the unsaturated and saturated zones underlying the repository in three dimensions. Transport calculations for a representative radionuclide cation, 135 Cs, and anion, 99 Tc, are presented. Calculations such as these will be used to study the effectiveness of the site's geochemical barriers at a mechanistic level and to help guide the geochemical site characterization program. The preliminary calculations should be viewed as a demonstration of the modeling methodology rather than as a study of the effectiveness of the geochemical barriers. The model provides a method for examining the integration of flow scenarios with transport and retardation processes as currently understood for the site. The effects on transport of many of the processes thought to be active at Yucca Mountain may be examined using this approach. 11 refs., 14 figs., 1 tab

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

Evaluation of CO2-Fluid-Rock Interaction in Enhanced Geothermal Systems: Field-Scale Geochemical Simulations

Directory of Open Access Journals (Sweden)

Feng Pan

2017-01-01

Full Text Available Recent studies suggest that using supercritical CO2 (scCO2 instead of water as a heat transmission fluid in Enhanced Geothermal Systems (EGS may improve energy extraction. While CO2-fluid-rock interactions at “typical” temperatures and pressures of subsurface reservoirs are fairly well known, such understanding for the elevated conditions of EGS is relatively unresolved. Geochemical impacts of CO2 as a working fluid (“CO2-EGS” compared to those for water as a working fluid (H2O-EGS are needed. The primary objectives of this study are (1 constraining geochemical processes associated with CO2-fluid-rock interactions under the high pressures and temperatures of a typical CO2-EGS site and (2 comparing geochemical impacts of CO2-EGS to geochemical impacts of H2O-EGS. The St. John’s Dome CO2-EGS research site in Arizona was adopted as a case study. A 3D model of the site was developed. Net heat extraction and mass flow production rates for CO2-EGS were larger compared to H2O-EGS, suggesting that using scCO2 as a working fluid may enhance EGS heat extraction. More aqueous CO2 accumulates within upper- and lower-lying layers than in the injection/production layers, reducing pH values and leading to increased dissolution and precipitation of minerals in those upper and lower layers. Dissolution of oligoclase for water as a working fluid shows smaller magnitude in rates and different distributions in profile than those for scCO2 as a working fluid. It indicates that geochemical processes of scCO2-rock interaction have significant effects on mineral dissolution and precipitation in magnitudes and distributions.

Geochemical baseline studies of soil in Finland

Science.gov (United States)

Pihlaja, Jouni

2017-04-01

The soil element concentrations regionally vary a lot in Finland. Mostly this is caused by the different bedrock types, which are reflected in the soil qualities. Geological Survey of Finland (GTK) is carrying out geochemical baseline studies in Finland. In the previous phase, the research is focusing on urban areas and mine environments. The information can, for example, be used to determine the need for soil remediation, to assess environmental impacts or to measure the natural state of soil in industrial areas or mine districts. The field work is done by taking soil samples, typically at depth between 0-10 cm. Sampling sites are chosen to represent the most vulnerable areas when thinking of human impacts by possible toxic soil element contents: playgrounds, day-care centers, schools, parks and residential areas. In the mine districts the samples are taken from the areas locating outside the airborne dust effected areas. Element contents of the soil samples are then analyzed with ICP-AES and ICP-MS, Hg with CV-AAS. The results of the geochemical baseline studies are published in the Finnish national geochemical baseline database (TAPIR). The geochemical baseline map service is free for all users via internet browser. Through this map service it is possible to calculate regional soil baseline values using geochemical data stored in the map service database. Baseline data for 17 elements in total is provided in the map service and it can be viewed on the GTK's web pages (http://gtkdata.gtk.fi/Tapir/indexEN.html).

Geochemical Investigations of Groundwater Stability

Energy Technology Data Exchange (ETDEWEB)

Bath, Adrian [Intellisci Ltd., Loughborough (United Kingdom)

2006-05-15

The report describes geochemical parameters and methods that provide information about the hydrodynamic stability of groundwaters in low permeability fractured rocks that are potential hosts for radioactive waste repositories. Hydrodynamic stability describes the propensity for changes in groundwater flows over long timescales, in terms of flow rates and flow directions. Hydrodynamic changes may also cause changes in water compositions, but the related issue of geochemical stability of a potential repository host rock system is outside the scope of this report. The main approaches to assessing groundwater stability are numerical modelling, measurement and interpretation of geochemical indicators in groundwater compositions, and analyses and interpretations of secondary minerals and fluid inclusions in these minerals. This report covers the latter two topics, with emphasis on geochemical indicators. The extent to which palaeohydrogeology and geochemical stability indicators have been used in past safety cases is reviewed. It has been very variable, both in terms of the scenarios considered, the stability indicators considered and the extent to which the information was explicitly or implicitly used in assessing FEPs and scenarios in the safety cases. Geochemical indicators of hydrodynamic stability provide various categories of information that are of hydrogeological relevance. Information about groundwater mixing, flows and water sources is potentially provided by the total salinity of groundwaters, their contents of specific non-reactive solutes (principally chloride) and possibly of other solutes, the stable isotopic ratio of water, and certain characteristics of secondary minerals and fluid inclusions. Information pertaining directly to groundwater ages and the timing of water and solute movements is provided by isotopic systems including tritium, carbon-14, chlorine-36, stable oxygen and hydrogen isotopes, uranium isotopes and dissolved mobile gases in

Principles of the landscape-geochemical and radio-ecological mapping of the territory polluted by technogenic radionuclides

International Nuclear Information System (INIS)

Sobotovich, Eh.V.; Shestopalov, V.M.; Pushkarev, A.V.; Mezhdunardonyj Nauchnyj Tsentr' Institut Chernobylya' Ukrainskogo Otdeleniya Vsemirnoj Laboratorii, Kiev; Institut Sel'skokhozyajstvennoj Radiologii, Akademii Agrarnykh Nauk Ukrainy, Kiev; Gosudarstvennoe Geologicheskoe Predpriyatie 'Geoprogn oz' Goskomiteta Geologii i Ispol'zovaniya Nedr Ukrainy, Kiev; AN Ukrainskoj SSR, Kiev

1993-01-01

The conceptual and methodical principles of radio-ecological mapping of the territory polluted by radionuclides as a result of catastrophe at the Chernobyl Nuclear Power Plant are reported. The radio-ecological mapping is based on the landscape-geochemical mapping of the polluted territory which is regarded as a unique natural-technogenic geochemical province. The ecological risk for the inhabitants residing here depends both on the degree and nature of pollution by radionuclides and on the landscape-geochemical factors influencing the radionuclide redistribution and secondary accumulation in different biosphere elements. It is substantiated as necessary to compile three types of radio-ecological maps which are of different purpose: control over the economic activities, protection of the population viability, the prediction of radio-ecological situation and the informing of population

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

Directory of Open Access Journals (Sweden)

Giuseppe Sappa

2013-03-01

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

Concerning initial and secondary character of radionuclide distribution in elementary landscape geochemical systems

Science.gov (United States)

Korobova, Elena; Romanov, Sergey

2017-04-01

Specificity of radionuclide distribution in elementary landscape geochemical systems (ELGS) treated as local system of geochemically linked elementary terrestrial units (in toposequence: watershed-slope-closing depression), belongs to one of the less investigated but practically significant problems of current geochemistry. First measurements after the Chernobyl accident showed a considerable variation of Cs-137 distribution in all examined ELGS (Shcheglov et al, 2001; Romanov, 1989; Korobova, Korovaykov, 1990; Linnik, 2008). The results may be interpreted in frames of two alternative hypotheses: 1) irregularity of the initial contamination; 2) secondary redistribution of the initially regular level of fallout. But herewith only a disproof of the first hypothesis automatically justifies the second one. Factors responsible for initial irregularity of surface contamination included: 1) the presence of the so-called "hot" particles in the initial fallout; 2) interception of radionuclides by forest canopy; 3) irregular aerial particles deposition; 4) uneven initial precipitation. Basing on monitoring Cs-137 spatial distribution that has been performed since 2005, we demonstrate that the observed spatial irregularity in distribution of Cs-137 in ELGS reflects a purely secondary distribution of initial reserves of radionuclides in fallout matter due to its migration with water in local geochemical systems. This statement has some significant consequences. 1. Mechanism of migration of matter in ELGS is complicated and could not be reduced solely to a primitive moving from watershed to closing depression. 2. The control of migration of "labeled atoms" (Cs-137) permits to understand common mechanism of migration of water in all systems on the level of ELGS. 3. Understanding formation of the structure of contamination zones in ELGS permits to use mathematical model to solve the inverse problem of restoration of the initially equable level of their contamination. Performed

Operative and informative nuclear-physical methods for analysis of mineral raw materials and control of technological process

International Nuclear Information System (INIS)

Sattarov, G.S.; Muzafarov, A.M.; Komilov, J.M.; Kadirov, F.; Kist, A.A.

2006-01-01

Full text: In the Navoi region uranium and gold are mined for more than 35 and 30 years, respectively. Various nuclear-chemical and nuclear-physical analysis methods are applied for elemental analysis of gold and uranium bearing ores and technological elements. The nuclear-physical analysis methods have a number of advantages: high sensitivity, capabilities for simultaneous determination of a number of elements, capabilities for automation of analysis process and their expressness at determination of short-living radionuclides. In the given work the comparative characteristics of nuclear-physical methods are shown applied for operative control of gold, uranium and some other rare elements at technological separation processes by sampling and at continuous flow of crushed ore and solution. They are: control of gold sorption leaching; quality control of ore, gravio- and flotation concentrate; x-ray spectral analysis; x-ray energy disperse analysis; radio-indicator and gamma-absorption analysis methods; neutron-activation analysis with using the ampoule neutron sources; elemental analysis at continuous flow of crushed ore and solution; and others. The analytical capabilities of some developed nuclear-physical research methods, which provide information on for geochemical and technological behaviour of gold, uranium and accompanying elements. Like photo-registration of radioluminescence; neutron-activation autoradiography and radio scanning; natural radiation radiometry; alpha, beta and gamma spectrometry of naturally active samples; determination of form in which the elements are present in sewage and underground waters; study of leachability of elements in dynamical and static conditions; determination of time of products being in technological apparatus. Practical examples are presented showing application of the developed methods for the study of geochemical behaviour of main and accompanying elements; for control of the gold, uranium, and some other rare and

Geochemical Processes Controlling Migration of High Level Wastes in Hanford's Vadose Zone

International Nuclear Information System (INIS)

Zachara, John M.; Serne, R. Jeffrey; Freshley, Mark D.; Mann, Frederick M.; Anderson, Frank J.; Wood, Marcus I.; Jones, Thomas E.; Myers, David A.

2007-01-01

High level nuclear wastes (HLW) from Hanford's plutonium reprocessing are stored in massive, buried, single-shell tanks in eighteen tank farms. The wastes were initially hot because of radioactive decay, and many exhibited extreme chemical character in terms of pH, salinity, and radionuclide concentration. At present, 67 of the 149 single shell tanks are suspected to have released over 1.9 million L of tank waste to the vadose zone, with most leak events occurring between 1950 and 1975. Boreholes have been placed through the largest vadose zone plumes to define the extent of contaminant migration, and to develop conceptual models of processes governing the transformation, retardation, and overall transport of tank waste residuals. Laboratory studies with sediments so collected have shown that ion exchange, precipitation and dissolution, and surface complexation reactions have occurred between the HLW and subsurface sediments moderating their chemical character, and retarding the migration of select contaminants. Processes suspected to facilitate the far-field migration of immobile radionuclides including stable aqueous complex formation and mobile colloids were found to be potentially operative, but unlikely to occur in the field, with the exception of cyanide-facilitated migration of 60Co. Fission product oxyanions are the most mobile of tank waste constituents because their adsorption is suppressed by large concentrations of waste anions; the vadose zone clay fraction is negative in surface charge; and, unlike Cr, their reduced forms are unstable in oxidizing environments. Reaction/process-based transport modeling is beginning to be used for predictions of future contaminant mobility and plume evolution

Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona

Science.gov (United States)

Wenrich, K.J.; Aumente-Modreski, R. M.

1994-01-01

Thousands of solution-collapse breccia pipes crop out in the canyons and on the plateaus of northwestern Arizona; some host high-grade uranium deposits. The mineralized pipes are enriched in Ag, As, Ba, Co, Cu, Mo, Ni, Pb, Sb, Se, V and Zn. These breccia pipes formed as sedimentary strata collapsed into solution caverns within the underlying Mississippian Redwall Limestone. A typical pipe is approximately 100 m (300 ft) in diameter and extends upward from the Redwall Limestone as much as 1000 m (3000 ft). Unmineralized gypsum and limestone collapses rooted in the Lower Permian Kaibab Limestone or Toroweap Formation also occur throughout this area. Hence, development of geochemical tools that can distinguish these unmineralized collapse structures, as well as unmineralized breccia pipes, from mineralized breccia pipes could significantly reduce drilling costs for these orebodies commonly buried 300-360 m (1000-1200 ft) below the plateau surface. Design and interpretation of soil sampling surveys over breccia pipes are plagued with several complications. (1) The plateau-capping Kaibab Limestone and Moenkopi Formation are made up of diverse lithologies. Thus, because different breccia pipes are capped by different lithologies, each pipe needs to be treated as a separate geochemical survey with its own background samples. (2) Ascertaining true background is difficult because of uncertainties in locations of poorly-exposed collapse cones and ring fracture zones that surround the pipes. Soil geochemical surveys were completed on 50 collapse structures, three of which are known mineralized breccia pipes. Each collapse structure was treated as an independent geochemical survey. Geochemical data from each collapse feature were plotted on single-element geochemical maps and processed by multivariate factor analysis. To contrast the results between geochemical surveys (collapse structures), a means of quantifying the anomalousness of elements at each site was developed. This

Orientation geochemical survey for uranium exploration using 230Th

International Nuclear Information System (INIS)

Xia Dingliang.

1985-01-01

The distribution of 230 Th in soils, rocks and ores and its relationship with respect to uranium ore formation are discussed for its possible use in geochemical exploration for U. 230 Th, U and Ra, being members of the same decay series, are different in their geochemical behavior upon which the study is orientated. Twenty uranium deposits and occurrences located in western and southern Hunan province are tested. Geochemical data obtained are comprehensively correlated. It is suggested that 230 Th is useful not only in U-Ra disequilibrium study but also in understanding the geochemical evolution of U ores. The data aid to interpret the genesis of uranium deposits and to assess the radioactive anomalies and uranium-bearing zones. Therefore, it can be adopted as a tool for searching in deep-buried uranium ores. The field procedure is rather simple and flexible to meet any geological environment. It is easy to read out and is less influnced by any kind of interference. In case of disequilibrium caused by oxidation and reduction during the period of ore formation it still gives good indication compared with that of radiometry, radonmetry and geochemical sampling for U

Quantification of source-term profiles from near-field geochemical models

International Nuclear Information System (INIS)

McKinley, I.G.

1985-01-01

A geochemical model of the near-field is described which quantitatively treats the processes of engineered barrier degradation, buffering of aqueous chemistry by solid phases, nuclide solubilization and transport through the near-field and release to the far-field. The radionuclide source-terms derived from this model are compared with those from a simpler model used for repository safety analysis. 10 refs., 2 figs., 2 tabs

Control of As and Ni releases from a uranium mill tailings neutralization circuit: Solution chemistry, mineralogy and geochemical modeling of laboratory study results

Energy Technology Data Exchange (ETDEWEB)

Mahoney, John [MWH Americas, Inc., 1801 California Street, Denver, CO 80202 (United States)], E-mail: john.j.mahoney@mwhglobal.com; Slaughter, Maynard [Earth Science, University of Northern Colorado, Greeley, CO 80639 (United States); Langmuir, Donald [Hydrochem Systems Corp., P.O. Box 23257, Silverthorne, CO 80498 (United States); Rowson, John [AREVA Resources Canada Inc., P.O. Box 9204, Saskatoon, SK, S7K 3X5 (Canada)

2007-12-15

Processing U ores in the JEB Mill of the McClean Lake Operation in northern Saskatchewan produces spent leaching solutions (raffinates) with pH {<=} 1.5, and As and Ni concentrations up to 6800 and 5200 mg L{sup -1}, respectively. Bench-scale neutralization experiments (pH 2-8) were performed to help optimize the design of mill processes for reducing As and Ni concentrations in tailings and raffinates to {<=}1 mg L{sup -1} prior to their disposal. Precipitate mineralogy determined by chemical analysis, XRD, SEM, EM, XM and EXAFS methods, included gypsum (the dominant precipitate), poorly crystalline scorodite (precipitated esp. from pH 2-4), annabergite, hydrobasaluminite, ferrihydrite, green rust II and theophrastite. The As was mostly in scorodite with smaller amounts in annabergite and trace As adsorbed and/or co-precipitated, probably by ferrihydrite. Geochemical modeling indicated that above pH 2, the ion activity product (IAP) of scorodite lies between the solubility products of amorphous and crystalline phases (log K{sub sp} = -23.0 and -25.83, respectively). The IAP decreases with increasing pH, suggesting that the crystallinity of the scorodite increases with pH. Forward geochemical models support the assumption that during neutralization, particles of added base produce sharp local pH gradients and disequilibrium with bulk solutions, facilitating annabergite and theophrastite precipitation.

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Zane Hills, Hughes and Shungnak quadrangles, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential.The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska.For this report, DGGS funded reanalysis of 105 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Zane Hills area in the Hughes and Shungnak quadrangles, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated into the statewide geochemical databases of both agencies.

Brent coal typing by combined optical and geochemical studies

Energy Technology Data Exchange (ETDEWEB)

Ducazeaux, J.; Le Tran, K.; Nicolas, G. (Societe Nationale des Petroles d' Aquitaine (SNPA), 64 - Pau (France))

1991-12-01

Palynological,petrographical and organic geochemical studies show that various kinds of coal occur throughout the Middle Jurassic Brent Group in the Viking Graben. Two types of coal with strong contrast in terms of source rock potential are thoroughly investigated in this study. It is found that they are relevant to two distinct organic facies. Though having the same organic carbon content, they are very different with respect to the petroleum generating potential, one being a conventional gas-prone coal of type III kerogen and the other one of type II-(III) kerogen which should be considered as an oil-generating coal. Explanations are sought for the difference observed, both geochemically and optically. Palynological study shows the occurrence of two distinct communities of land plants in relation with the depositional environment and climatic changes, whilst coal petrographical study shows that the macerals are unevenly and differently distributed in these two coal types. The original organic material and the depositional environment appear to be the main controlling factors. 13 Refs.; 8 Figs.

Robust statistics and geochemical data analysis

International Nuclear Information System (INIS)

Di, Z.

1987-01-01

Advantages of robust procedures over ordinary least-squares procedures in geochemical data analysis is demonstrated using NURE data from the Hot Springs Quadrangle, South Dakota, USA. Robust principal components analysis with 5% multivariate trimming successfully guarded the analysis against perturbations by outliers and increased the number of interpretable factors. Regression with SINE estimates significantly increased the goodness-of-fit of the regression and improved the correspondence of delineated anomalies with known uranium prospects. Because of the ubiquitous existence of outliers in geochemical data, robust statistical procedures are suggested as routine procedures to replace ordinary least-squares procedures

Coupling of transport and geochemical models

International Nuclear Information System (INIS)

Noy, D.J.

1985-01-01

This contract stipulated separate pieces of work to consider mass transport in the far-field of a repository, and more detailed geochemical modelling of the groundwater in the near-field. It was envisaged that the far-field problem would be tackled by numerical solutions to the classical advection-diffusion equation obtained by the finite element method. For the near-field problem the feasibility of coupling existing geochemical equilibrium codes to the three dimensional groundwater flow codes was to be investigated. This report is divided into two sections with one part devoted to each aspect of this contract. (author)

Integrated geophysical-geochemical methods for archaeological prospecting

OpenAIRE

Persson, Kjell

2005-01-01

A great number of field measurements with different methods and instruments were conducted in attempts to develop a method for an optimal combination of various geochemical and geophysical methods in archaeological prospecting. The research presented in this thesis focuses on a study of how different anthropogenic changes in the ground can be detected by geochemical and geophysical mapping and how the results can be presented. A six-year pilot project, Svealand in Vendel and Viking periods (S...

Retention/sorption and geochemical modelling

Energy Technology Data Exchange (ETDEWEB)

Arcos, D.; Grandia, F.; Domenech, C. [Enviros Spain, S.L., Barcelona (Spain); SCK-CEN, Mol (Belgium); Sellin, P. [SKB - Swedish Nuclear Fuel and Waste Management, SE, Stockholm (Sweden); Hunter, F.M.I.; Bate, F.; Heath, T.G.; Hoch, A. [Serco Assurance, Oxfordshire (United Kingdom); Werme, L.O. [SKB - Svensk Karnbranslehantering AB, Stockholm (Sweden); Bruggeman, C.; Maes, I.A.; Breynaert, E.; Vancluysen, J. [Leuven Katholieke Univ., Lab. for Colloid Chemistry (Belgium); Montavon, G.; Guo, Z. [Ecole des Mines, 44 - Nantes (France); Riebe, B.; Bunnenberg, C.; Meleshyn, A. [Leibniz Univ. Hannover, Zentrum fur Strahlenschutz und Radiookologie, Hannover (Germany); Dultz, S. [Leibniz Univ. Hannover, Institut fur Bodenkunde, Hannover (Germany)

2007-07-01

This session gathers 4 articles dealing with: the long-term geochemical evolution of the near field of a KBS-3 HLNW repository: insights from reactive transport modelling (D. Arcos, F. Grandia, C. Domenech, P. Sellin); the investigation of iron transport into bentonite from anaerobically corroding steel: a geochemical modelling study (F.M.I. Hunter, F. Bate, T.G. Heath, A. Hoch, L.O. Werme); SeO{sub 3}{sup 2-} adsorption on conditioned Na-illite: XAS spectroscopy, kinetics, surface complexation model and influence of compaction (C. Bruggeman, A. Maes, G. Montavon, E. Breynaert, Z. Guo, J. Vancluysen); the influence of temperature and gamma-irradiation on the anion sorption capacity of modified bentonites (B. Riebe, C. Bunnenberg, A. Meleshyn, S. Dultz)

Geochemical prospect ion results of Treinta y Tres aerial photo

International Nuclear Information System (INIS)

Zeegers, H.; Bonnefoy, D.; Garau, M.; Spangenberg, J.

1981-01-01

This report shows the geochemical prospect ion results carried out within the framework of the multielemental geochemical strategy. The samples were studied by e spectrometry in the laboratories of Orleans.

Geochemical processes controlling groundwater quality under semi arid environment: A case study in central Morocco.

Science.gov (United States)

Karroum, Morad; Elgettafi, Mohammed; Elmandour, Abdenabi; Wilske, Cornelia; Himi, Mahjoub; Casas, Albert

2017-12-31

Bahira plain is an important area for Morocco due to its agriculture and mining activities. Situated in a sub-arid to arid climate, this plain hosts an aquifer system that represents sequences of carbonates, phosphates, evaporates and alluvial deposits. Groundwater flows from Ganntour plateau (recharge area) to the basin-fill deposits and Zima Lake and Sed Elmejnoun where water evaporates. The objective of this study was to characterize the chemical properties of the groundwater and to assess the processes controlling the groundwater's chemistry. We can divide water samples into three hydrochemical water groups: recharge waters (Ca/Mg-HCO 3 ), transition zone waters (Ca-HCO 3 -SO 4 /Cl) and discharge waters (Na-Cl/SO 4 ). Accordingly, compositions of waters are determined by the availability of easily soluble minerals like calcite (Ca-HCO 3 dominant), halite (Na-Cl dominant) and gypsum (Ca-SO 4 dominant). Cl/Br ratios show that Cl concentration increases from dissolution of natural halite. When groundwater is affected by extreme evaporation Cl/Br ratios may increase up to 1900. High fluoride concentrations are associated with low Ca 2+ concentrations (<100mg/L). That means when recharge waters enter the aquifer, it starts dissolving fluorite since the Ca 2+ concentration is low. Once groundwater becomes saturated with Ca 2+ , the immobilization of fluoride is occurring by precipitation of fluoride-rich minerals like fluoro-apatite. According to the environmental isotope ( 18 O and 2 H) analyses, they are three potential processes affecting groundwater: 1. Evaporation as verified by low slope value, 2. Water-rock interaction, 3. admixture of waters showed different stable isotope compositions and salinities. Copyright © 2017 Elsevier B.V. All rights reserved.

Geochemical behaviour of uranium in the cycle of alteration

International Nuclear Information System (INIS)

Chervet, J.; Coulomb, R.

1958-01-01

The investigation of the genesis of secondary mineralized accumulations, and the prospecting of deposits from microchemical anomalies in the surface material, is requiring a well-developed knowledge of the geochemical properties of the uranium during the alteration phase. In the present work, the authors tried to track the uranium history during a part of his natural creeping. a) They describe some most typical mineralogical observations of alteration phenomena and material migration, picked up in place on the deposits. b) They give experimental results concerning the solubilities of the uranium minerals and the factors affecting this solubility. c) They study the water circulation in granitic batholites, and the influence of the occurrence of the uranium deposits on their composition. d) They observe the amplitude of phenomena restricting the dispersions: fixations, precipitations, etc., and the behaviour of growth in uraniferous areas. e) Finally, the opposition chemical alteration-radioactive equilibrium results in an important imbalance in altered materials. The authors tried to use the measurement of this imbalance to explain geochemical processes. (author) [fr

Geochemical normalization of magnetic susceptibility for investigation of floodplain sediments

Czech Academy of Sciences Publication Activity Database

Faměra, Martin; Matys Grygar, Tomáš; Elznicová, J.; Grison, Hana

2018-01-01

Roč. 77, č. 5 (2018), č. článku 189. ISSN 1866-6280 R&D Projects: GA ČR(CZ) GA15-00340S Institutional support: RVO:61388980 ; RVO:67985530 Keywords : Background functions * Geochemical normalization * Mass-specific magnetic susceptibility * Post-depositional processes * Provenance Subject RIV: DD - Geochemistry OBOR OECD: Environmental sciences (social aspects to be 5.7); Geology (GFU-E) Impact factor: 1.569, year: 2016

Geochemical Exploration Techniques Applicable in the Search for Copper Deposits

Science.gov (United States)

Chaffee, Maurice A.

1975-01-01

Geochemical exploration is an important part of copper-resource evaluation. A large number of geochemical exploration techniques, both proved and untried, are available to the geochemist to use in the search for new copper deposits. Analyses of whole-rock samples have been used in both regional and local geochemical exploration surveys in the search for copper. Analyses of mineral separates, such as biotite, magnetite, and sulfides, have also been used. Analyses of soil samples are widely used in geochemical exploration, especially for localized surveys. It is important to distinguish between residual and transported soil types. Orientation studies should always be conducted prior to a geochemical investigation in a given area in order to determine the best soil horizon and the best size of soil material for sampling in that area. Silty frost boils, caliche, and desert varnish are specialized types of soil samples that might be useful sampling media. Soil gas is a new and potentially valuable geochemical sampling medium, especially in exploring for buried mineral deposits in arid regions. Gaseous products in samples of soil may be related to base-metal deposits and include mercury vapor, sulfur dioxide, hydrogen sulfide, carbon oxysulfide, carbon dioxide, hydrogen, oxygen, nitrogen, the noble gases, the halogens, and many hydrocarbon compounds. Transported materials that have been used in geochemical sampling programs include glacial float boulders, glacial till, esker gravels, stream sediments, stream-sediment concentrates, and lake sediments. Stream-sediment sampling is probably the most widely used and most successful geochemical exploration technique. Hydrogeochemical exploration programs have utilized hot- and cold-spring waters and their precipitates as well as waters from lakes, streams, and wells. Organic gel found in lakes and at stream mouths is an unproved sampling medium. Suspended material and dissolved gases in any type of water may also be useful

Geochemical behaviour of natural uranium-series nuclides in geological formation

International Nuclear Information System (INIS)

Yamakawa, Minoru

1991-01-01

Recent research and investigation show that the Tono uranium deposit and its natural uranium-series nuclides have been preserved, without any significant changes like re-migration or reconcentration, throughout geological events such as upheaval-submergence, marine transgression-regression, and faulting which can readily change geological, hydrogeological, and geochemical conditions. This situation might have come about as a result of being kept in a geometrical closure system, with reducing and milk alkalic geochemical conditions, from the hydrogeological and geochemical point of view. (author)

Process control device

International Nuclear Information System (INIS)

Hayashi, Toshifumi; Kobayashi, Hiroshi.

1994-01-01

A process control device comprises a memory device for memorizing a plant operation target, a plant state or a state of equipments related with each other as control data, a read-only memory device for storing programs, a plant instrumentation control device or other process control devices, an input/output device for performing input/output with an operator, and a processing device which conducts processing in accordance with the program and sends a control demand or a display demand to the input/output device. The program reads out control data relative to a predetermined operation target, compares and verify them with actual values to read out control data to be a practice premise condition which is further to be a practice premise condition if necessary, thereby automatically controlling the plant or requiring or displaying input. Practice presuming conditions for the operation target can be examined succesively in accordance with the program without constituting complicated logical figures and AND/OR graphs. (N.H.)

Geochemical prospecting for thorium and uranium deposits

International Nuclear Information System (INIS)

Boyle, R.W.

1982-01-01

The basic purpose of this book is to present an analysis of the various geochemical methods applicable in the search for all types of thorium and uranium deposits. The general chemistry and geochemistry of thorium and uranium are briefly described in the opening chapter, and this is followed by a chapter on the deposits of the two elements with emphasis on their indicator (pathfinder) elements and on the primary and secondary dispersion characteristics of thorium and uranium in the vicinity of their deposits. The next seven chapters form the main part of the book and describe geochemical prospecting for thorium and uranium, stressing selection of areas in which to prospect, radiometric surveys, analytical geochemical surveys based on rocks (lithochemical surveys), unconsolidated materials (pedochemical surveys), natural waters and sediments (hydrochemical surveys), biological materials (biogeochemical surveys), gases (atmochemical surveys), and miscellaneous methods. A final brief chapter reviews radiometric and analytical methods for the detection and estimation of thorium and uranium. (Auth.)

Alligator Rivers Analogue project. Geochemical modelling of present-day groundwaters. Final Report - Volume 12

Energy Technology Data Exchange (ETDEWEB)

Sverjensky, D A [The John Hopkins Univ, Dept of Earth and Planetary Sciences, Baltimore (United States)

1993-12-31

The main purpose of this report is to summarize geochemical modeling studies of the present-day Koongarra groundwaters. Information on the present-day geochemistry and geochemical processes at Koongarra forms a basis for a present-day analogue for nuclear waste migration. The present-day analogue is built on studies of the mineralogy and petrology of the Koongarra deposit, and chemical analyses of present-day groundwaters from the deposit. The overall approach taken in the present study has been to carry out a series of aqueous speciation and state of saturation calculations, including chemical mass transfer calculations, to address the possible control over the chemistry of the present-day for the groundwaters at Koongarra. The most important implication of the present study for the migration of radionuclides is the strong role played by the water-rock interactions, both above and below the water table, influencing the overall chemical evolution of the groundwaters. Thus, the results show that the chemical evolution of waters is strongly controlled by the initial availability of CO{sub 2} and the mineral assemblage encountered, which together determine the major element evolution of the waters by controlling the pH. The relative rates of evolution of the pH and the oxidation state of the groundwaters are also critical to the mobility of uranium. The shallow Koongarra waters are sufficiently oxidising that they can dissolve and transport uranium even under acidic conditions. Under the more reducing condition of the deep groundwaters, is the pH level that permits uranium transport as carbonate complexes. However, if the oxidation state decreases to much lower levels, it would be expected that uranium become immobile. All the speciation and state of saturation calculations carried out in the present study are available from the author, on request 22 refs., 7 tabs., 18 figs.

Alligator Rivers Analogue project. Geochemical modelling of present-day groundwaters. Final Report - Volume 12

Energy Technology Data Exchange (ETDEWEB)

Sverjensky, D. A. [The John Hopkins Univ, Dept of Earth and Planetary Sciences, Baltimore (United States)

1992-12-31

The main purpose of this report is to summarize geochemical modeling studies of the present-day Koongarra groundwaters. Information on the present-day geochemistry and geochemical processes at Koongarra forms a basis for a present-day analogue for nuclear waste migration. The present-day analogue is built on studies of the mineralogy and petrology of the Koongarra deposit, and chemical analyses of present-day groundwaters from the deposit. The overall approach taken in the present study has been to carry out a series of aqueous speciation and state of saturation calculations, including chemical mass transfer calculations, to address the possible control over the chemistry of the present-day for the groundwaters at Koongarra. The most important implication of the present study for the migration of radionuclides is the strong role played by the water-rock interactions, both above and below the water table, influencing the overall chemical evolution of the groundwaters. Thus, the results show that the chemical evolution of waters is strongly controlled by the initial availability of CO{sub 2} and the mineral assemblage encountered, which together determine the major element evolution of the waters by controlling the pH. The relative rates of evolution of the pH and the oxidation state of the groundwaters are also critical to the mobility of uranium. The shallow Koongarra waters are sufficiently oxidising that they can dissolve and transport uranium even under acidic conditions. Under the more reducing condition of the deep groundwaters, is the pH level that permits uranium transport as carbonate complexes. However, if the oxidation state decreases to much lower levels, it would be expected that uranium become immobile. All the speciation and state of saturation calculations carried out in the present study are available from the author, on request 22 refs., 7 tabs., 18 figs.

Geochemical and hydrodynamic controls on arsenic and trace metal cycling in a seasonally stratified US sub-tropical reservoir

International Nuclear Information System (INIS)

Brandenberger, Jill M.; Louchouarn, Patrick; Herbert, Bruce; Tissot, Philippe

2004-01-01

The phase distribution of trace metals and oxyanions was investigated within a South Texas watershed hosting a high density of surface uranium mine pits and tailings. The objectives of the study were to evaluate the potential impact of these old uranium mining sites on the watershed with particular emphasis on spatial and temporal changes in water quality of a reservoir that serves as the major source of freshwater to a population of ∼ 350,000 people in the region. A livestock pond, bordered by uranium mine tailings, was used as a model case-study site to evaluate the cycling of uranium mine-derived oxyanions under changing redox conditions. Although the pond showed seasonal thermal and chemical stratification, geochemical cycling of metals was limited to Co and Pb, which seemed to be mostly associated with redox cycling of Mn mineral phases, and U, which suggested reductive precipitation in the ponds hypolimnion. Uranium levels, however, were too low to support strong inputs from th e tailings into the water column of the pond. The strong relations observed between particulate Cr, Cs, V and Fe suggest that these metals are associated with a stable particulate phase (probably allochthonous aluminosilicates) enriched in unreactive iron. This observation is supported by a parallel relationship in sediments collected across a broad range of sediment depositional processed (and histories) in the basin. Arsenic, though selectively enriched in the ponds water column, remained stable and mostly in solution throughout the depth of the profile and showed no sign of geochemical cycling or interaction with Fe-rich particles. We found no evidence of anthropogenic impacts of U mines beyond the purely local scale. Arsenic does decrease in concentration downstream of uranium mining sites but its presence within the Nueces drainage basin is related to interactions between surface and ground waters with uranium-rich geological formations rather than long-scale transport of

Geochemical and hydrodynamic controls on arsenic and trace metal cycling in a seasonally stratified US sub-tropical reservoir

International Nuclear Information System (INIS)

Brandenberger, J.; Louchouarn, P.; Herbert, B.; Tissot, P.

2004-01-01

The phase distribution of trace metals and oxyanions, including U and As, in 2 surface water bodies was investigated within a South Texas watershed hosting a high density of surface U mine pits and tailings. The objectives of the study were to evaluate the environmental legacy of U mining, with particular emphasis on the spatial and temporal variability of water quality in Lake Corpus Christi, a downstream reservoir that serves as the major water resource to a population of ∼350,000 people in the region. Lyssy Pond, a livestock pond bordered by U mine tailings, was used as a model case-study site to evaluate the cycling of U mine-derived oxyanions under changing redox conditions. Although the pond showed seasonal thermal and chemical stratification, geochemical cycling of metals was limited to Co and Pb, which was correlated with redox cycling of Mn mineral phases, and U, which suggested reductive precipitation in the pond's hypolimnion. Uranium levels, however, were too low to support strong inputs from the tailings into the water column of the pond. The strong relationships observed between particulate Cr, Cs, V, and Fe suggest that these metals are associated with a stable particulate phase (probably allochthonous alumino-silicates) enriched in unreactive Fe. This observation is supported by a parallel relationship in sediments collected across a broad range of sediment depositional processes (and histories) in the basin. Arsenic, though selectively enriched in the pond's water column, was dominated by dissolved species throughout the depth of the profile and showed no sign of geochemical cycling or interaction with Fe-rich particles. Arsenic (and other oxyanions) in the water columns of Lake Corpus Christi and Lyssy pond were not affected by the abundant presence of Fe-rich particles but instead behaved conservatively. No evidence was found of anthropogenic impacts of U mines beyond the purely local scale. Arsenic's presence within the Nueces drainage basin

Applications of prospecting geochemical techniques to the search for and to the study of uranium deposits in metropolitan France

International Nuclear Information System (INIS)

Grimbert, Arnold

1957-01-01

After having recalled facts which leaded the CEA to use new geochemical techniques for the prospecting of uranium deposits through sampling and analysis of soils and waters, the author describes the organisation and methods implemented for this prospecting activity: team composition for sampling and analysis, role of each engineer and technician in the prospecting stages (preliminary study, routine prospecting, result interpretation), sampling and analysis processes. He also reports campaigns of geochemical prospecting: study of the La Chapelle Largeau deposit (objectives, geological context, preliminary study, routine prospecting, study of geochemical anomalies), tactical research on Verneix indices (study of radioactivity anomaly discovered by radio-prospecting), strategical searches in a non prospected area in the South of Avallon. The author discusses the issues of efficiency and cost price of this geochemical prospecting technique in soils and in waters. Appendices present the equipment and operation modality for soil sampling, and for soil sample preparation, and principles, equipment and products for soil analysis and for water analysis [fr

Experimental study and numerical modelling of geochemical reactions occurring during uranium in situ recovery (ISR) mining

International Nuclear Information System (INIS)

Ben Simon, R.

2011-09-01

The in situ Recovery (ISR) method consists of ore mining by in situ chemical leaching with acid or alkaline solutions. ISR takes place underground and is therefore limited to the analysis of the pumped solutions, hence ISR mine management is still empirical. Numerical modelling has been considered to achieve more efficient management of this process. Three different phenomena have to be taken into account for numerical simulations of uranium ISR mining: (1) geochemical reactions; (2) the kinetics of these reactions, and (3) hydrodynamic transport with respect to the reaction kinetics. Leaching tests have been conducted on ore samples from an uranium mine in Tortkuduk (Kazakhstan) where ISR is conducted by acid leaching. Two types of leaching experiments were performed: (1) tests in batch reactors; and (2) extraction in flow through columns. The assumptions deduced from the leaching tests were tested and validated by modelling the laboratory experiments with the numerical codes CHESS and HYTEC, both developed at the Geosciences research center of Mines ParisTech. A well-constrained 1D hydrogeochemical transport model of the ISR process at laboratory-scale was proposed. It enables to translate the chemical release sequence that is observed during experiments into a geochemical reaction sequence. It was possible to highlight the controlling factors of uranium dissolution, and the precipitation of secondary mineral phase in the deposit, as well as the determination of the relative importance of these factors. (author)

A Low-Li Geochemical Province in the NE Atlantic

DEFF Research Database (Denmark)

Bailey, J. C.; Gwozdz, R.

1978-01-01

Lithium was analysed in 392 basalts and related igneous rocks from the North Atlantic Tertiary-Recent province using activation analysis and Čerenkov counting. Monotonous Li values of 5.5±2 ppm in NE Atlantic basalts define a low-Li geochemical province which has persisted for 60 million years...... basalt series. No whole-rock coherence is observed between Li and Mg, K, Rb or Ca. Mantle phlogopite is considered to play an insignificant rôle in controlling the Li levels of NE Atlantic basalts....

Analysis of the geochemical gradient created by surface-groundwater interactions within riverbanks of the East River in Crested Butte, Colorado

Science.gov (United States)

Lunzer, J.; Williams, K. H.; Malenda, H. F.; Nararne-Sitchler, A.

2016-12-01

An improved understanding of the geochemical gradient created by the mixing of surface and groundwater of a river system will have considerable impact on our understanding of microorganisms, organic cycling and biogeochemical processes within these zones. In this study, the geochemical gradient in the hyporheic zone is described using a variety of geochemical properties. A system of shallow groundwater wells were installed in a series of transects along a stream bank. Each transect consists of several wells that progress away from the river bank in a perpendicular fashion. From these wells, temperature, conductivity and pH of water samples were obtained via hand pumping or bailing. These data show a clear geochemical gradient that displays a distinct zone in the subsurface where the geochemical conditions change from surface water dominated to groundwater dominated. For this study, the East River near Crested Butte, Colorado has been selected as the river of interest due the river being a relatively undisturbed floodplain. Additionally, the specific section chosen on the East River displays relatively high sinuosity meaning that these meandering sections will produce hyporheic zones that are more laterally expansive than what would be expected on a river of lower sinuosity. This increase in lateral extension of the hyporheic zone will make depicting the subtle changes in the geochemical gradient much easier than that of a river system in which the hyporheic zone is not as laterally extensive. Data has been and will be continued to be collected at different river discharges to evaluate the geochemical gradient at differing rates. Overall, this characterization of the geochemical gradient along stream banks will produce results that will aid in the further use of geochemical methods to classify and understand hyporheic exchange zones and the potential expansion of these techniques to river systems of differing geologic and geographic conditions.

Geochemical behavior of disposed radioactive waste

International Nuclear Information System (INIS)

Barney, G.S.; Navratil, J.D.; Schulz, W.W.

1984-01-01

The papers in this book are organized to cover the chemical aspects that are important to understanding the behavior of disposed radioactive wastes. These aspects include radionuclide sorption and desorption, solubility of radionuclide compounds, chemical species of radionuclides in natural waters, hydrothermal geochemical reactions, measurements of radionuclide migration, solid state chemistry of wastes, and waste-form leaching behavior. The information in each of the papers is necessary to predict the transport of radionuclides from wastes via natural waters and thus to predict the safety of the disposed waste. Radionuclide transport in natural waters is strongly dependent on sorption, desorption, dissolution, and precipitation processes. The first two papers discuss laboratory investigations of these processes. Descriptions of sorption and desorption behavior of important radionuclides under a wide range of environmental conditions are presented in the first section. Among the sorbents studied are basalt interbed solids, granites, clays, sediments, hydrous oxides, and pure minerals. Effects of redox conditions, groundwater composition and pH on sorption reactions are described

Environmental Transport of Plutonium: Biogeochemical Processes at Femtomolar Concentrations and Nanometer Scales

Energy Technology Data Exchange (ETDEWEB)

Kersting, Annie B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2010-10-05

The major challenge in predicting the mobility and transport of plutonium (Pu) is determining the dominant geochemical processes that control its behavior in the subsurface. The reaction chemistry of Pu (i.e., aqueous speciation, solubility, sorptivity, redox chemistry, and affinity for colloidal particles, both abiotic and microbially mediated) is particularly complicated. It is generally thought that due to its low solubility and high sorptivity, Pu migration in the environment occurs only when facilitated by transport on particulate matter (i.e., colloidal particles). Despite the recognized importance of colloid-facilitated transport of Pu, very little is known about the geochemical and biochemical mechanisms controlling Pu-colloid formation and association, particularly at femtomolar Pu concentrations observed at DOE sites.

Controls on the geochemical evolution of Prairie Pothole Region lakes and wetlands over decadal time scales

Science.gov (United States)

Goldhaber, Martin B.; Mills, Christopher T.; Mushet, David M.; McCleskey, R. Blaine; Rover, Jennifer

2016-01-01

One hundred sixty-seven Prairie Pothole lakes, ponds and wetlands (largely lakes) previously analyzed chemically during the late 1960’s and early to mid-1970’s were resampled and reanalyzed in 2011–2012. The two sampling periods differed climatically. The earlier sampling took place during normal to slightly dry conditions, whereas the latter occurred during and immediately following exceptionally wet conditions. As reported previously in Mushet et al. (2015), the dominant effect was expansion of the area of these lakes and dilution of their major ions. However, within that context, there were significant differences in the evolutionary pathways of major ions. To establish these pathways, we employed the inverse modeling computer code NetpathXL. This code takes the initial and final lake composition and, using mass balance constrained by the composition of diluting waters, and input and output of phases, calculates plausible geochemical evolution pathways. Despite the fact that in most cases major ions decreased, a subset of the lakes had an increase in SO42−. This distinction is significant because SO42− is the dominant anion in a majority of Prairie Pothole Region wetlands and lakes. For lakes with decreasing SO42−, the proportion of original lake water required for mass balance was subordinate to rainwater and/or overland flow. In contrast, lakes with increasing SO42− between the two sampling episodes tended to be dominated by original lake water. This suite of lakes tended to be smaller and have lower initial SO42−concentrations such that inputs of sulfur from dissolution of the minerals gypsum or pyrite had a significant impact on the final sulfur concentration given the lower dilution factors. Thus, our study provides context for how Prairie Pothole Region water bodies evolve geochemically as climate changes. Because wetland geochemistry in turn controls the ecology of these water bodies, this research contributes to the prediction of the

Geochemical effects on the behavior of LLW radionuclides in soil/groundwater environments

Energy Technology Data Exchange (ETDEWEB)

Krupka, K.M.; Sterne, R.J. [Pacific Northwest Lab., Richland, WA (United States)

1995-12-31

Assessing the migration potential of radionuclides leached from low-level radioactive waste (LLW) and decommissioning sites necessitates information on the effects of sorption and precipitation on the concentrations of dissolved radionuclides. Such an assessment requires that the geochemical processes of aqueous speciation, complexation, oxidation/reduction, and ion exchange be taken into account. The Pacific Northwest National Laboratory (PNNL) is providing technical support to the U.S. Nuclear Regulatory Commission (NRC) for defining the solubility and sorption behavior of radionuclides in soil/ground-water environments associated with engineered cementitious LLW disposal systems and decommissioning sites. Geochemical modeling is being used to predict solubility limits for radionuclides under geochemical conditions associated with these environments. The solubility limits are being used as maximum concentration limits in performance assessment calculations describing the release of contaminants from waste sources. Available data were compiled regarding the sorption potential of radionuclides onto {open_quotes}fresh{close_quotes} cement/concrete where the expected pH of the cement pore waters will equal to or exceed 10. Based on information gleaned from the literature, a list of preferred minimum distribution coefficients (Kd`s) was developed for these radionuclides. The K{sub d} values are specific to the chemical environments associated with the evolution of the compositions of cement/concrete pore waters.

Statistical interpretation of geochemical data

International Nuclear Information System (INIS)

Carambula, M.

1990-01-01

Statistical results have been obtained from a geochemical research from the following four aerial photographies Zapican, Carape, Las Canias, Alferez. They have been studied 3020 samples in total, to 22 chemical elements using plasma emission spectrometry methods.

Investigation of the geochemical evolution of groundwater under agricultural land: A case study in northeastern Mexico

Science.gov (United States)

Ledesma-Ruiz, Rogelio; Pastén-Zapata, Ernesto; Parra, Roberto; Harter, Thomas; Mahlknecht, Jürgen

2015-02-01

Zona Citrícola is an important area for Mexico due to its citriculture activity. Situated in a sub-humid to humid climate adjacent to the Sierra Madre Oriental, this valley hosts an aquifer system that represents sequences of shales, marls, conglomerates, and alluvial deposits. Groundwater flows from mountainous recharge areas to the basin-fill deposits and provides base flows to supply drinking water to the adjacent metropolitan area of Monterrey. Recent studies examining the groundwater quality of the study area urge the mitigation of groundwater pollution. The objective of this study was to characterize the physical and chemical properties of the groundwater and to assess the processes controlling the groundwater's chemistry. Correlation was used to identify associations among various geochemical constituents. Factor analysis was applied to identify the water's chemical characteristics that were responsible for generating most of the variability within the dataset. Hierarchical cluster analysis was employed in combination with a post-hoc analysis of variance to partition the water samples into hydrochemical water groups: recharge waters (Ca-HCO3), transition zone waters (Ca-HCO3-SO4 to Ca-SO4-HCO3) and discharge waters (Ca-SO4). Inverse geochemical models of these groups were developed and constrained using PHREEQC to elucidate the chemical reactions controlling the water's chemistry between an initial (recharge) and final water. The primary reactions contributing to salinity were the following: (1) water-rock interactions, including the weathering of evaporitic rocks and dedolomitization; (2) dissolution of soil gas carbon dioxide; and (3) input from animal/human wastewater and manure in combination with by denitrification processes. Contributions from silicate weathering to salinity ranged from less important to insignificant. The findings suggest that it may not be cost-effective to regulate manure application to mitigate groundwater pollution.

Baseline and premining geochemical characterization of mined sites

Science.gov (United States)

Nordstrom, D. Kirk

2015-01-01

A rational goal for environmental restoration of new, active, or inactive mine sites would be ‘natural background’ or the environmental conditions that existed before any mining activities or other related anthropogenic activities. In a strictly technical sense, there is no such thing as natural background (or entirely non-anthropogenic) existing today because there is no part of the planet earth that has not had at least some chemical disturbance from anthropogenic activities. Hence, the terms ‘baseline’ and ‘pre-mining’ are preferred to describe these conditions. Baseline conditions are those that existed at the time of the characterization which could be pre-mining, during mining, or post-mining. Protocols for geochemically characterizing pre-mining conditions are not well-documented for sites already mined but there are two approaches that seem most direct and least ambiguous. One is characterization of analog sites along with judicious application of geochemical modeling. The other is reactive-transport modeling (based on careful synoptic sampling with tracer-injection) and subtracting inputs from known mining and mineral processing. Several examples of acidic drainage are described from around the world documenting the range of water compositions produced from pyrite oxidation in the absence of mining. These analog sites provide insight to the processes forming mineralized waters in areas untouched by mining. Natural analog water-chemistry data is compared with the higher metal concentrations, metal fluxes, and weathering rates found in mined areas in the few places where comparisons are possible. The differences are generally 1–3 orders of magnitude higher for acid mine drainage.

Geochemical fingerprints and controls in the sediments of an urban river: River Manzanares, Madrid (Spain)

International Nuclear Information System (INIS)

Miguel, Eduardo de; Charlesworth, Susanne; Ordonez, Almudena; Seijas, Eduardo

2005-01-01

The geochemical fingerprint of sediment retrieved from the banks of the River Manzanares as it passes through the City of Madrid is presented here. The river collects the effluent water from several Waste Water Treatment (WWT) plants in and around the city, such that, at low flows, up to 60% of the flow has been treated. A total of 18 bank-sediment cores were collected along the course of the river, down to its confluence with the Jarama river, to the south-east of Madrid. Trace and major elements in each sample were extracted following a double protocol: (a) 'Total' digestion with HNO 3 , HClO 4 and HF; (b) 'Weak' digestion with sodium acetate buffered to pH=5 with acetic acid, under constant stirring. The digests thus obtained were subsequently analysed by ICP-AES, except for Hg which was extracted with aqua regia and sodium chloride-hydroxylamine sulfate, and analysed by Cold Vapour-AAS. X-ray diffraction was additionally employed to determine the mineralogical composition of the samples. Uni- and multivariate analyses of the chemical data reveal the influence of Madrid on the geochemistry of Manzanares' sediments, clearly manifested by a marked increase in the concentration of typically 'urban' elements Ag, Cr, Cu, Pb and Zn, downstream of the intersection of the river with the city's perimeter. The highest concentrations of these elements appear to be associated with illegal or accidental dumping of waste materials, and with the uncontrolled incorporation of untreated urban runoff to the river. The natural matrix of the sediment is characterised by fairly constant concentrations of Ce, La and Y, whereas changes in the lithology intersected by the river cause corresponding variations in Ca-Mg and Al-Na contents. In the final stretch of the river, the presence of carbonate materials seems to exert a strong geochemical control on the amount of Zn and, to a lesser extent, Cu immobilised in the sediments. This fact suggests that a variable but significant

Geochemical investigation of UMTRAP designated site at Durango, Colorado

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report is the result of a geochemical investigation of the former uranium mill and tailings site at Durango, Colorado. This is one in a series of site specific geochemical investigations performed on the inactive uranium mill tailings included in the UMTRA Project. The objectives of the investigation are to characterize the geochemistry, to determine the contaminant distribution resulting from the former milling activities and tailings, and to infer chemical pathways and transport mechanisms from the contaminant distribution. The results will be used to model contaminant migration and to develop criteria for long-term containment media such as a cover system which is impermeable to contaminant migration. This report assumes a familiarity with the hydrologic conditions of the site and the geochemical concepts underlying the investigation. The results reported are based on a one-time sampling of waters and solid material from the background, the area adjacent to the site, and the site. The solid samples are water extracted remove easily soluble salts and acids extracted to remove cabonates and hydroxides. The water extracts and solid samples were analyzed for the major and trace elements. A limited number of samples were analyzed for radiological components. The report includes the methods of sampling, sample processing, analysis, and data interpretation. Three major conclusions are: (1) carbonate salts and low TDS characterize the tailings; (2) the adjacent area and raffinate ponds contain contaminants deposited by a single event of fluid permeation of the soils; and (3) the Animas River adjacent to the site has elevated gross alpha activity attributed to 226 Ra in the sediments derived from the tailings or milling activities

Regional geochemical maps of uranium in Northern Scotland. Environmental and economic considerations

International Nuclear Information System (INIS)

Plant, J.

1978-01-01

The Institute of Geological Studies geochemical mapping programme is outlined. The natural levels of uranium in rocks, soils and waters are discussed. Some practical details of geochemical mapping are given. Applications of geochemical maps of uranium in Scotland are considered: economic applications and medical geography and agriculture. A list of 38 references is appended. (U.K.)

Uranium geochemical exploration in northwestern Luzon

International Nuclear Information System (INIS)

Santos, G. Jr.; Fernandez, L.; Ogena, M.; Tauli, G.

1980-01-01

A reconnaissance geochemical stream water and sediment survey which was conducted in northwestern Luzon was able to detect ten (10) uranium anomalous areas. These anomalous areas are located along a north-south trending zone of Miocene marine clastics and sedimentary rocks with tuffaceous sediment intercalations. In general, northwest Luzon has low radioactivity except for two anomalous areas which have 3 to 6 times background radioactivity. Radon anomalies occur in sparsely scattered locations. The anomalous zones appear to be related to major north-south faults and secondary northeast-southwest trending structures. Geochemical correlations between uranium and other elements such as copper, lead, zinc, manganese, silver, cobalt and nickel are generally very poor. (author)

A geochemical approach to distinguishing competing tectono-magmatic processes preserved in small eruptive centres

Science.gov (United States)

McGee, Lucy E.; Brahm, Raimundo; Rowe, Michael C.; Handley, Heather K.; Morgado, Eduardo; Lara, Luis E.; Turner, Michael B.; Vinet, Nicolas; Parada, Miguel-Ángel; Valdivia, Pedro

2017-06-01

Small eruptive centres (SECs) representing short-lived, isolated eruptions are effective samples of mantle heterogeneity over a given area, as they are generally of basaltic composition and show evidence of little magmatic processing. This is particularly powerful in volcanic arcs where the original melting process generating stratovolcanoes is often obscured by additions from the down-going slab (fluids and sediments) and the overlying crust. The Pucón area of southern Chile contains active and dormant stratovolcanoes, Holocene, basaltic SECs and an arc-scale strike-slip fault (the Liquiñe Ofqui Fault System: LOFS). The SECs show unexpected compositional heterogeneity considering their spatial proximity. We present a detailed study of these SECs combining whole rock major and trace element concentrations, U-Th isotopes and olivine-hosted melt inclusion major element and volatile contents to highlight the complex inter-relations in this small but active area. We show that heterogeneity preserved at individual SECs relates to different processes: some start in the melting region with the input of slab-derived fluids, whilst others occur later in a centre's magmatic history with the influence of crustal contamination prior to olivine crystallisation. These signals are deduced through the combination of the different geochemical tools used in this study. We show that there is no correlation between composition and distance from the arc front, whilst the local tectonic regime has an effect on melt composition: SECs aligned along the LOFS have either equilibrium U-Th ratios or small Th-excesses instead of the large—fluid influenced—U-excesses displayed by SECs situated away from this feature. One of the SECs is modelled as being generated from fluid-enriched depleted mantle, a source which it may share with the stratovolcano Villarrica, whilst another SEC with abundant evidence of crustal contamination may share its plumbing system with its neighbouring

Evolution of geochemical conditions in SFL 3-5

International Nuclear Information System (INIS)

Karlsson, Fred; Lindgren, M.; Skagius, K.; Wiborgh, M.; Engkvist, I.

1999-12-01

The evolution of geochemical conditions in the repository for long-lived low- and intermediate-level waste, SFL 3-5, and in the vicinity of the repository are important when predicting the retention of radionuclides and the long-term stability of engineered barriers. In this study the initial conditions at different repository sites at 300 - 400 m depth, the influence of repository construction and operation, the expected conditions after repository closure and saturation, and the evolution in a long-term perspective are discussed. Groundwaters that are found at these depths have near-neutral pH and are reducing in character, but the composition can vary from saline to non-saline water. The water chemistry in the near-field will mainly be influenced by the composition of the groundwater and by the large amounts of cementitious material that can be found in the repository. Disturbances caused during construction and operation are not expected to be permanent. Studies of old concrete indicate that leaching of concrete is a slow process. The geochemical conditions in the repository are therefore expected to be stable and prevail for hundreds of thousand years. However, the evolution of the surrounding environment may influence the conditions in long-term perspective

Evolution of geochemical conditions in SFL 3-5

Energy Technology Data Exchange (ETDEWEB)

Karlsson, Fred [Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden); Lindgren, M.; Skagius, K.; Wiborgh, M. [Kemakta Konsult AB, Stockholm (Sweden); Engkvist, I. [Barsebaeck Kraft AB (Sweden)

1999-12-01

The evolution of geochemical conditions in the repository for long-lived low- and intermediate-level waste, SFL 3-5, and in the vicinity of the repository are important when predicting the retention of radionuclides and the long-term stability of engineered barriers. In this study the initial conditions at different repository sites at 300 - 400 m depth, the influence of repository construction and operation, the expected conditions after repository closure and saturation, and the evolution in a long-term perspective are discussed. Groundwaters that are found at these depths have near-neutral pH and are reducing in character, but the composition can vary from saline to non-saline water. The water chemistry in the near-field will mainly be influenced by the composition of the groundwater and by the large amounts of cementitious material that can be found in the repository. Disturbances caused during construction and operation are not expected to be permanent. Studies of old concrete indicate that leaching of concrete is a slow process. The geochemical conditions in the repository are therefore expected to be stable and prevail for hundreds of thousand years. However, the evolution of the surrounding environment may influence the conditions in long-term perspective.

Metal pollution in a contaminated bay: Relationship between metal geochemical fractionation in sediments and accumulation in a polychaete

International Nuclear Information System (INIS)

Fan, Wenhong; Xu, Zhizhen; Wang, Wen-Xiong

2014-01-01

Jinzhou Bay in Northern China has been seriously contaminated with metals due to the impacts of smelting activities. In this study, we investigated the relationship between metal accumulation in a deposit-feeding polychaete Neanthes japonica and metal concentration and geochemical fractionation (Cd, Cu, Pb, Zn and Ni) in sediments of Jinzhou Bay. Compared with the historical data, metals in the more mobile geochemical fraction (exchangeable and carbonate fractions) were gradually partitioned into the more stable fraction (Fe–Mn oxides) over time. Metal concentration and geochemical fractionation in sediment significantly affected metal bioavailability and accumulation in polychaetes, except for Ni. Metal accumulation in polychaetes was significantly influenced by Fe or Mn content, and to a lesser degree by organic matter. Prediction of metal bioaccumulation in polychaetes was greatly improved by normalizing metal concentrations to Mn content in sediment. The geochemical fractionation of metals in sediments including the exchangeable, organic matter and Fe–Mn oxides were important in controlling the sediment metal bioavailability to polychaetes. - Highlights: • Metals in contaminated sediments gradually partitioned into the more stable phase over time. • Metal accumulation in polychaetes was more significantly influenced by Fe/Mn content than by organic matter. • Prediction of metal bioaccumulation greatly improved by normalizing metals to Mn content in sediment. • Metals in exchangeable, organic matter and Fe–Mn oxides were important in controlling their bioavailability. - Prediction of metal bioaccumulation in polychaetes was significantly improved by normalizing metal concentrations to Mn content in sediment

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Kougarok area, Bendeleben and Teller quadrangles, Seward Peninsula, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 302 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Kougarok River drainage as well as smaller adjacent drainages in the Bendeleben and Teller quadrangles, Seward Peninsula, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated

Geochemical modelling of bentonite porewater in high-level waste repositories

Science.gov (United States)

Wersin, Paul

2003-03-01

The description of the geochemical properties of the bentonite backfill that serves as engineered barrier for nuclear repositories is a central issue for perfomance assessment since these play a large role in determining the fate of contaminants released from the waste. In this study the porewater chemistry of bentonite was assessed with a thermodynamic modelling approach that includes ion exchange, surface complexation and mineral equilibrium reactions. The focus was to identify the geochemical reactions controlling the major ion chemistry and acid-base properties and to explore parameter uncertainties specifically at high compaction degrees. First, the adequacy of the approach was tested with two distinct surface complexation models by describing recent experimental data performed at highly varying solid/liquid ratios and ionic strengths. The results indicate adequate prediction of the entire experimental data set. Second, the modelling was extended to repository conditions, taking as an example the current Swiss concept for high-level waste where the compacted bentonite backfill is surrounded by argillaceous rock. The main reactions controlling major ion chemistry were found to be calcite equilibrium and concurrent Na-Ca exchange reactions and de-protonation of functional surface groups. Third, a sensitivity analysis of the main model parameters was performed. The results thereof indicate a remarkable robustness of the model with regard to parameter uncertainties. The bentonite system is characterised by a large acid-base buffering capacity which leads to stable pH-conditions. The uncertainty in pH was found to be mainly induced by the pCO 2 of the surrounding host rock. The results of a simple diffusion-reaction model indicate only minor changes of porewater composition with time, which is primarily due to the geochemical similarities of the bentonite and the argillaceous host rock. Overall, the results show the usefulness of simple thermodynamic models to

Geochemical processes in a calcareous sandstone aquifer during managed aquifer recharge with desalinated seawater

Science.gov (United States)

Ganot, Yonatan; Russak, Amos; Siebner, Hagar; Bernstein, Anat; Katz, Yoram; Guttman, Jospeh; Kurtzman, Daniel

2017-04-01

In the last three years we monitor Managed Aquifer Recharge (MAR) of post-treated desalinated seawater (PTDES) in an infiltration pond, at the Menashe site that overlies the northern part of the Israeli Coastal Aquifer. The PTDES are stabilized with CaCO3 during post-treatment in the desalination plant and their chemical composition differs from those of any other water recharged to the aquifer and of the natural groundwater. We use suction cups in the unsaturated zone, shallow observation wells within the pond and production wells that encircles the MAR Menashe site, to study the geochemical processes during MAR with PTDES. Ion-enrichment (remineralization) of the recharged water was observed in both unsaturated zone and shallow observation wells samples. Enrichment occurs mainly in the first few meters below the pond surface by ion-exchange processes. Mg2+ enrichment is most prominent due to its deficiency in the PTDES. It is explained by ion-exchange with Ca2+, as the PTDES (enriched with Ca2+) infiltrates through a calcareous-sandstone aquifer with various amount of adsorbed Mg2+ (3-27 meq/kg). Hence, the higher concentration of Ca+2 in the PTDES together with its higher affinity to the sediments promotes the release of Mg2+ ions to the recharged water. Water isotopes analysis of the production wells were used to estimate residence time and mixing with local groundwater. At the end of 2016, it was found that the percentage of PTDES in adjacent down-gradient production wells was around 10%, while more distant or up-gradient wells show no mixing with PTDES. The distinct isotope contrast between the recharged desalinated seawater (δ2H=+11.2±0.2‰) and the local groundwater (δ2H ranged from -22.7 to -16.7‰) is a promising tool to evaluate future mixing processes at the Menshae MAR site. Using the Menashe MAR system for remineralization could be beneficial as a primary or complementary post-treatment technique. However, the sustainability of this process is

Cross-correlation analysis of 2012-2014 seismic events in Central-Northern Italy: insights from the geochemical monitoring network of Tuscany

Science.gov (United States)

Pierotti, Lisa; Facca, Gianluca; Gherardi, Fabrizio

2015-04-01

Since late 2002, a geochemical monitoring network is operating in Tuscany, Central Italy, to collect data and possibly identify geochemical anomalies that characteristically occur before regionally significant (i.e. with magnitude > 3) seismic events. The network currently consists of 6 stations located in areas already investigated in detail for their geological setting, hydrogeological and geochemical background and boundary conditions. All these stations are equipped for remote, continuous monitoring of selected physicochemical parameters (temperature, pH, redox potential, electrical conductivity), and dissolved concentrations of CO2 and CH4. Additional information are obtained through in situ discrete monitoring. Field surveys are periodically performed to guarantee maintenance and performance control of the sensors of the automatic stations, and to collect water samples for the determination of the chemical and stable isotope composition of all the springs investigated for seismic precursors. Geochemical continuous signals are numerically processed to remove outliers, monitoring errors and aseismic effects from seasonal and climatic fluctuations. The elaboration of smoothed, long-term time series (more than 200000 data available today for each station) allows for a relatively accurate definition of geochemical background values. Geochemical values out of the two-sigma relative standard deviation domain are inspected as possible indicators of physicochemical changes related to regional seismic activity. Starting on November 2011, four stations of the Tuscany network located in two separate mountainous areas of Northern Apennines separating Tuscany from Emilia-Romagna region (Equi Terme and Gallicano), and Tuscany from Emilia-Romagna and Umbria regions (Vicchio and Caprese Michelangelo), started to register anomalous values in pH and CO2 partial pressure (PCO2). Cross-correlation analysis indicates an apparent relationship between the most important seismic

Factors of the accumulation of heavy metals and metalloids at geochemical barriers in urban soils

Science.gov (United States)

Kosheleva, N. E.; Kasimov, N. S.; Vlasov, D. V.

2015-05-01

The bulk contents and concentrations of mobile (extracted by an ammonium acetate buffer with EDTA) Cd, Pb, Sb, As, Bi, Zn, and Cu were determined in the surface horizons of urban soils in the Eastern administrative okrug of Moscow. The regression analysis showed that the accumulation of these metals and metalloids in the soils is controlled by the physicochemical soil properties and by number of anthropogenic factors and landscape conditions (geochemical position, type of loose deposits, character of land use, dust load, vehicle emissions, building pattern, percent of green areas, and the extent of sealed soils). The precipitation of studied elements on the geochemical barriers had the following regularities: Cd, Cu, and Zn accumulated on the alkaline barriers; Bi, Sb, As, Cu, Pb, and Zn, on chemisorption barriers; Sb, As, and Pb, on organomineral barriers; and Cd and Cu, on the sorption-sedimentation barriers. Technogenic transformation of the physicochemical properties of urban soils resulted in the increase of the mean bulk contents of heavy metals and metalloids by 33-99%; the portion of elements fixed on the geochemical barriers increased by 26-50%.

Lead Isotopes in Olivine-Phyric Shergottite Tissint: Implications for the Geochemical Evolution of the Shergottite Source Mantle

Science.gov (United States)

Moriwaki, R.; Usui, T.; Simon, J. I.; Jones, J. H.; Yokoyama, T.

2015-01-01

Geochemically-depleted shergottites are basaltic rocks derived from a martian mantle source reservoir. Geochemical evolution of the martian mantle has been investigated mainly based on the Rb-Sr, Sm-Nd, and Lu-Hf isotope systematics of the shergottites [1]. Although potentially informative, U-Th- Pb isotope systematics have been limited because of difficulties in interpreting the analyses of depleted meteorite samples that are more susceptible to the effects of near-surface processes and terrestrial contamination. This study conducts a 5-step sequential acid leaching experiment of the first witnessed fall of the geochemically-depleted olivinephyric shergottite Tissint to minimize the effect of low temperature distrubence. Trace element analyses of the Tissint acid residue (mostly pyroxene) indicate that Pb isotope compositions of the residue do not contain either a martian surface or terrestrial component, but represent the Tissint magma source [2]. The residue has relatively unradiogenic initial Pb isotopic compositions (e.g., 206Pb/204Pb = 10.8136) that fall within the Pb isotope space of other geochemically-depleted shergottites. An initial µ-value (238U/204Pb = 1.5) of Tissint at the time of crystallization (472 Ma [3]) is similar to a time-integrated mu- value (1.72 at 472 Ma) of the Tissint source mantle calculated based on the two-stage mantle evolution model [1]. On the other hand, the other geochemically-depleted shergottites (e.g., QUE 94201 [4]) have initial µ-values of their parental magmas distinctly lower than those of their modeled source mantle. These results suggest that only Tissint potentially reflects the geochemical signature of the shergottite mantle source that originated from cumulates of the martian magma ocean

A hydro-geochemical study of Nahr-Ibrahim catchment area: Fluvial metal transport

International Nuclear Information System (INIS)

Korfali, Samira

2004-01-01

Author.Metals enter water bodies geological weathering, soil erosion, industrial and domestic waste discharges, as well as atmospheric deposition. The metal content in sediments is a reflection of the nature of their background whether of geologic and/or anthropogenic origin. The depositional process of metals in sediment are controlled by river discharge, turbulence of river, morphology and river geometry, as well as the geochemical phases of sediment and soils. Thus a study of metal content in river and /or metal transport with a water body should include a hydrological study of the river, types of minerals in sediment and soil, sediment and soil textures, and metal speciation in the different geochemical phases of sediment, bank and soils. A contaminated flood plain is a temporary storage system for pollutants and an understanding of soil-sediment-interactions is important prerequisite for modeling fluvial pollutant transport. The determination of metal speciation in sediment and soil chemical fraction can provide information on the way in which these metals are bound to sediment and soil, their mobilization potential, bioavailability and possible mechanism of fluvial pollutant transport. Sequential extraction techniques yielding operationally defined chemical pools have been used by many workers to examine the partitioning of metals among the various geochemical phases of sediment or soil. The sequential extraction method specifies metals in sediment fractions as: exchangeable, specifically sorbed, easily reducible, moderately reducible, organic, residual. Previously, I have conducted a study on speciation of metals (Fe, Mn, Zn, Cu, Pb and Cd) in the dry season bed-load sediments only at five sites 13 km stretch upstream from the mouth of Nahr Ibrahim. The reported data revealed that the specifically sorbed sediment fraction was the prime fraction for deposition of Mn, Z, CU, Pb and Cd metals in sediments. X-ray diffraction analysis of bed sediments showed

Granite-repository - geochemical environment

International Nuclear Information System (INIS)

1979-04-01

Some geochemical data of importance for a radioactive waste repository in hard rock are reviewed. The ground water composition at depth is assessed. The ground water chemistry in the vicinity of uranium ores is discussed. The redox system in Swedish bedrock is described. Influences of extreme climatic changes and of repository mining and construction are also evaluated

Geochemical behavior of uranium mill tailings leachate in the subsurface

International Nuclear Information System (INIS)

Brookins, D.G.

1993-01-01

Leachate generated from surface disposal of acidic uranium mill tailings at Maybell, CO has impacted groundwater quality within the underlying mineralized Browns Park Formation. The extent of groundwater contamination, however, is located directly beneath the tailings impoundment. The milling process consisted of sulfuric acid extraction of uranium from the feed ore by a complex chemical leaching and precipitation process. Tailings leachate at the site contains elevated concentrations of Al, As, Cd, Mo, Ni, NO 3 , Se, U, and other solutes. From column leach tests, the concentrations of contaminants within tailings pore fluid are SO 4 >NH 4 >NO 3 >U>Se>Ni>As>Cd at pH 4.0. The carbonate buffering capacity of the tailings subsoil has decreased because of calcite dissolution in the presence of acidic leachate. Groundwater quality data, mineralogical and microbiological studies, and geochemical modeling suggest that As, NO 3 , Se, U and other solutes are being removed from solution through precipitation, adsorption, and denitrification processes under reducing conditions. Presence of hydrogen sulfide, liquid and gaseous hydrocarbons, dissolved organic, and abundant pyrite within the Browns Park Formations have maintained reducing conditions subjacent to the tailings impoundment. Groundwater is in close equilibrium with coffinite and uraninite, the primary U(IV) minerals extracted from the Browns Parks Formation. Denitrifying bacteria identified in this study catalyze redox reactions involving NO 3 . Subsequently, contaminant distributions of NO 3 decrease 1000 times beneath the tailings impoundment. Applying geochemical and biochemical processes occurring at Maybell provides an excellent model for in situ aquifer restoration programs considered at other uranium tailings and heavy-metal-mixed waste contaminated sites. (author) 4 figs., 4 tabs., 27 refs

Biological reduction of chlorinated solvents: Batch-scale geochemical modeling

Science.gov (United States)

Kouznetsova, Irina; Mao, Xiaomin; Robinson, Clare; Barry, D. A.; Gerhard, Jason I.; McCarty, Perry L.

2010-09-01

Simulation of biodegradation of chlorinated solvents in dense non-aqueous phase liquid (DNAPL) source zones requires a model that accounts for the complexity of processes involved and that is consistent with available laboratory studies. This paper describes such a comprehensive modeling framework that includes microbially mediated degradation processes, microbial population growth and decay, geochemical reactions, as well as interphase mass transfer processes such as DNAPL dissolution, gas formation and mineral precipitation/dissolution. All these processes can be in equilibrium or kinetically controlled. A batch modeling example was presented where the degradation of trichloroethene (TCE) and its byproducts and concomitant reactions (e.g., electron donor fermentation, sulfate reduction, pH buffering by calcite dissolution) were simulated. Local and global sensitivity analysis techniques were applied to delineate the dominant model parameters and processes. Sensitivity analysis indicated that accurate values for parameters related to dichloroethene (DCE) and vinyl chloride (VC) degradation (i.e., DCE and VC maximum utilization rates, yield due to DCE utilization, decay rate for DCE/VC dechlorinators) are important for prediction of the overall dechlorination time. These parameters influence the maximum growth rate of the DCE and VC dechlorinating microorganisms and, thus, the time required for a small initial population to reach a sufficient concentration to significantly affect the overall rate of dechlorination. Self-inhibition of chlorinated ethenes at high concentrations and natural buffering provided by the sediment were also shown to significantly influence the dechlorination time. Furthermore, the analysis indicated that the rates of the competing, nonchlorinated electron-accepting processes relative to the dechlorination kinetics also affect the overall dechlorination time. Results demonstrated that the model developed is a flexible research tool that is

Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration

Energy Technology Data Exchange (ETDEWEB)

Teng, H. Henry [PI, The George Washington University; Xu, Huifang [Co-PI, University of Wisconsin-Madison

2013-07-17

We have approached the long-standing geochemical question why anhydrous high-Mg carbonate minerals (i.e., magnesite and dolomite) cannot be formed at ambient conditions from a new perspective by exploring the formation of MgCO{sub 3} and Mg{sub x}Ca{sub (1-x)}CO{sub 3} in non-aqueous solutions. Data collected from our experiments in this funding period suggest that a fundamental barrier, other than cation hydration, exists that prevents Mg{sup 2+} and CO{sub 3}{sup 2-} ions from forming long-range ordered structures. We propose that this barrier mainly stems from the lattice limitation on the spatial configuration of CO{sub 3} groups in magnesite crystals. On the other hand, the measured higher distribution coefficients of Mg between magnesian calcites formed in the absence and presence of water give us a first direct proof to support and quantify the cation hydration effect.

Predictive Analysis of Geochemical Controls in an Alpine Stream

Science.gov (United States)

Jochems, A. P.; Sherson, L. R.; Crossey, L. J.; Karlstrom, K. E.

2010-12-01

Alpine watersheds are increasingly relied upon for use in the American West, necessitating a more complete understanding of annual hydrologic patterns and geologic influences on water chemistry. The Jemez River is a fifth order stream in central New Mexico that flows from its source in the Jemez Mountains to its confluence with the Rio Grande north of the town of Bernalillo. Designated uses of the Jemez River include domestic water supply, recreation, and agriculture. Geothermal uses are currently being considered as well. The river recharges shallow aquifer waters used by several communities, including tribal lands of the Jemez Pueblo. The hydrogeology of the Jemez system is characterized by geothermal inputs from the Baca hydrothermal system associated with the 1.2Ma Valles caldera, as well as groundwater and surface water interactions. Freshwater input from the Rio Guadalupe and several ephemeral tributaries also influences the water chemistry of the Jemez system. Fifteen sites along a 35 km reach of the river were sampled between 2006 and 2010. Discharge of the Jemez River ranged from 10-876 cfs over the study period. The annual hydrograph is affected by annual snowmelt in the Jemez Mountains as well as surges due to monsoonal rains in July and August. Geochemical data collected over this period include temperature, conductivity, pH, dissolved oxygen (D.O.), major ions, trace elements, and stable isotopes. Continuous records of temperature, conductivity, pH, D.O. and turbidity data were collected from a water quality sonde installed in March 2010. Geochemical modeling and time series analysis were performed using PHREEQC, Geochemist’s Workbench, and MATLAB. Empirical data collected during this study gave rise to several models describing the hydrology and geochemistry of the Jemez system. Our data suggest that springs are the primary contributors to dissolved load, and that solute loading from geothermal inputs is intensified by low flows observed on

Geochemical Characterization of the Upper and Middle Floridan Aquifer System, South Florida

Science.gov (United States)

Mirecki, J.; Richardson, E.; Bennett, M.; Hendel, J.

2008-05-01

Our study focus is to characterize the water quality and geochemical environment of the Floridan Aquifer System (FAS) throughout the regional flowpath. A synoptic survey of 21 wells (n=15, upper FAS; n=6 middle FAS) was supplemented by additional samples (n=11) obtained during exploratory well development at 4 aquifer storage recovery (ASR) pilot sites. Synoptic survey samples were analyzed intensively, yielding a dataset that consists of major and trace dissolved constituents (including metals), stable isotopes (δ18O, δ13C, δD, δ34S in sulfate and sulfide), carbon species (carbonate alkalinity and organic carbon), uranium-series radionuclides, nutrients, and selected microbes and pathogens. The objectives of this study are three-fold: 1) to provide baseline water-quality and geochemical information prior to initiation of ASR activities that are part of the Comprehensive Everglades Restoration Plan; 2) to quantify the major controls on geochemical evolution along upper and middle FAS flowpaths using geochemical modeling methods; and 3) to identify areas where water- quality may limit the feasibility of ASR methods in the FAS. Preliminary interpretations water quality changes along the regional FAS flowpath can be summarized as follows. Concentrations of dissolved constituents increase from north to south along the flow path; generally, the upper FAS has lower total dissolved solids than the middle FAS at locations where well pairs were analyzed. The redox environment changes from oxic to strongly anoxic, very close to the recharge area. Redox measurements, dissolved iron, sulfide, and sulfur isotope data are consistent with sulfate-reducing conditions. Uranium-series isotope concentrations and activities generally are below regulatory criteria, with few exceptions in both the upper and middle FAS. Areas with greater radionuclide activity occur primarily at distal flowpath locations or at the coast.

Petrological mineralogical and geochemical characterization of the granitoids and fracture fillings developed in Ratones Mines (Spain); Caracterizacion petrologica, mineralogica, geoquimica y evaluacion del comportamiento geoquimico de las REE en la fase solida (granitoides y rellenos fisurales) del sistema de interaccion agua-roca delentorno de la Mina Ratones

Energy Technology Data Exchange (ETDEWEB)

Buil Gutierrez, B [Ciemat. Madrid (Spain)

2002-07-01

The petrological, mineralogical and geochemical characterisation of the granitoids and fracture fillings developed in the Ratones Mine (Caceres, Spain) has been done in order to understand rock-water interaction processes which control water geochemical parameters. Special interest has been devoted to the analysis and interpretation of REE patterns in the solid phase (granitoids and fracture fillings) because they constitute geochemical tracers in water-rock interaction process. Moreover, REE are considered as actinide analogues. In order to characterise the solid phase (granitoids and fracture fillings) several investigation scales (system, outcrop, whole rock, mineral and geochemical components) have been considered and different types of samples have been analysed. These factors control the methodological approach used in this investigation. The analytical methods we have used in this investigation are microscope, qualitative and semi-quantitative methods (XRD, SEM,EDAX) and quantitative methods (ICP-MS, XRF, EM, LAM-IC-MS). The bulk of the granitoids located around the Ratones Mine Belongs to the alkaline feldspar granite-sienogranite lihotype and they show a peraluminous and subalkaline pattern. From the mineralogical point of view, they are composed by quartz, K-feldspar (Or>90%), showing sericitation, moscovitization and turmolinization altherations, alkaline plagioclase (An-=-3%), usually altered to sericite, saussirite and less frequently affected by moscovitization processes, Fe-Al biotite, frequently affected by chloritization processes and sometimes replaced by muscovite, and finally muscovite (>2% celadonite and <4% paragonite) both of primary and secondary origin. The differences observed between the different lithotypes are related with the modal proportion of the principal minerals,with the presence or absence of certain accessory minerals ( turmaline, cordierite), with specific textural patterns, grain size and also with the richness in specific

Geochemical Distribution of Lead and Chromium in River Getsi-Kano

African Journals Online (AJOL)

Geochemical forms of lead (Pb) and Chromium (Cr) from the sediment of River Getsi Kano-Nigeria were determined using Atomic Absorption spectrometer for eighteen months. Apart from determination of the metals in water, geochemical forms of the metals were also evaluated into five fractions. Exchangeable, bound to ...

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Haines area, Juneau and Skagway quadrangles, southeast Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 212 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Chilkat, Klehini, Tsirku, and Takhin river drainages, as well as smaller drainages flowing into Chilkat and Chilkoot Inlets near Haines, Skagway Quadrangle, Southeast Alaska. Additionally some samples were also chosen from the Juneau gold belt, Juneau Quadrangle, Southeast Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical

Izu-Bonin rear-arc magmatism: Geochemical investigation of volcanoclastic material

OpenAIRE

Sæbø, Andreas

2017-01-01

Studied samples from the Izu Bonin rear arc show a distinct geochemical pattern that resemble the modern continental crust. In contrast to the volcanic front, samples from the Izu Bonin rear arc show enrichment of LREE (La, Ce, Pr, Nd) and higher K2O at a given SiO2. This suggest that processes leading up to the geochemistry observed in the rear arc is fundamental in creating the modern continental crust. Additional isotopic and trace element analysis from volcanic material rec...

Geochemical prospecting in Guiana

International Nuclear Information System (INIS)

Coulomb, R.

1957-01-01

During the last few years geochemical prospecting techniques have become common usage in the field of mineral deposit prospecting. The real scope of these methods lies in their use in the prospecting of large areas. The most promising use of the geochemistry and hydro-geochemistry of uranium is in heavily forested tropical territories, with few outcrops, where radiometry is strongly handicapped. (author) [fr

GEOTECHNICAL/GEOCHEMICAL CHARACTERIZATION OF ADVANCED COAL PROCESS WASTE STREAMS

Energy Technology Data Exchange (ETDEWEB)

Edwin S. Olson; Charles J. Moretti

1999-11-01

Thirteen solid wastes, six coals and one unreacted sorbent produced from seven advanced coal utilization processes were characterized for task three of this project. The advanced processes from which samples were obtained included a gas-reburning sorbent injection process, a pressurized fluidized-bed coal combustion process, a coal-reburning process, a SO{sub x}, NO{sub x}, RO{sub x}, BOX process, an advanced flue desulfurization process, and an advanced coal cleaning process. The waste samples ranged from coarse materials, such as bottom ashes and spent bed materials, to fine materials such as fly ashes and cyclone ashes. Based on the results of the waste characterizations, an analysis of appropriate waste management practices for the advanced process wastes was done. The analysis indicated that using conventional waste management technology should be possible for disposal of all the advanced process wastes studied for task three. However, some wastes did possess properties that could present special problems for conventional waste management systems. Several task three wastes were self-hardening materials and one was self-heating. Self-hardening is caused by cementitious and pozzolanic reactions that occur when water is added to the waste. All of the self-hardening wastes setup slowly (in a matter of hours or days rather than minutes). Thus these wastes can still be handled with conventional management systems if care is taken not to allow them to setup in storage bins or transport vehicles. Waste self-heating is caused by the exothermic hydration of lime when the waste is mixed with conditioning water. If enough lime is present, the temperature of the waste will rise until steam is produced. It is recommended that self-heating wastes be conditioned in a controlled manner so that the heat will be safely dissipated before the material is transported to an ultimate disposal site. Waste utilization is important because an advanced process waste will not require

Geochemical study of water-rock interaction processes on geothermal systems of alkaline water in granitic massif; Estudio geoquimico de los procesos de interaccion agua-roca sobre sistemas goetermales de aguas alcalinas en granitoides

Energy Technology Data Exchange (ETDEWEB)

Buil gutierrez, B; Garcia Sanz, S; Lago San Jose, M; Arranz Uague, E; Auque Sanz, L [Universidad de Zaragoza (Spain)

2002-07-01

The study of geothermal systems developed within granitic massifs (with alkaline waters and reducing ORP values) is a topic of increasing scientific interest. These systems are a perfect natural laboratory for studying the water-rock interaction processes as they are defined by three main features: 1) long residence time of water within the system, 2) temperature in the reservoir high enough to favour reaction kinetics and finally, 3) the comparison of the chemistry of the incoming and outgoing waters of the system allows for the evaluation of the processes that have modified the water chemistry and its signature, The four geothermal systems considered in this paper are developed within granitic massifs of the Spanish Central Pyrenes; these systems were studied from a geochemical point of view, defining the major, trace and REE chemistry of both waters and host rocks and then characterizing the composition and geochemical evolution of the different waters. Bicarbonate-chloride-sodic and bicarbonate-sodic compositions are the most representative of the water chemistry in the deep geothermal system, as they are not affected by secondary processes (mixing, conductive cooling, etc). (Author)

Summary report on geochemical barrier special study

International Nuclear Information System (INIS)

1988-12-01

Long-term management of uranium mill tailings must provide assurance that soluble contaminants will not migrate beyond the Point of Compliance. Conventional management alternatives provide containment through the use of physical barriers which are designed to prevent migration of water through the tailings pile. An alternative is to geochemically modify the tailings to immobilize the contaminants. This investigation examined three potential geochemical modifiers to determine their ability to immobilize inorganic groundwater contaminants found in uranium mill tailings. These modifiers were hydrated lime (Ca(OH) 2 ), limestone (CaCO 3 ), and a sphaegnum peat moss. This investigation focused on both the geochemical interactions between the tailings and the modifiers, and the effects the modifiers had on the physical strength of the tailings. The geochemical investigations began with characterization of the tailings by X-ray diffraction and scanning electron microscopy. This was followed by batch leaching experiments in which various concentrations of each modifier were added to tailings in shaker flasks and allowed to come to equilibrium. Finally, column experiments were conducted to simulate flow through a tailings pile. The results show that all of the modifiers were at least moderately effective at immobilizing most of the groundwater contaminants of concern at uranium mill tailings sites. Hydrated lime was able to achieve 90 percent concentration reduction of arsenic, cadmium, selenium, uranium, and sulfate when added at a two percent concentration. Limestone was somewhat less effective and peat removed greater than 90 percent of arsenic, lead, uranium, and sulfate at a one percent concentration. The column tests showed that kinetic and/or mass transfer limitations are important and that sufficient time must be allowed for the immobilization reactions to occur

Proceedings of 2. Brazilian Geochemical Congress

International Nuclear Information System (INIS)

1989-01-01

Some works about geochemistry are presented, including themes about geochemical exploration, lithogeochemistry and isotope geochemistry, environmental geochemistry, analytical geochemistry, geochemistry of carbonatites and rare earth elements and organic geochemistry. (C.G.C.) [pt

Scientific fundamentals of the exploration and calculability of a waste repository. Project part III, sub-project 2: Validity and applicability of geochemical models

International Nuclear Information System (INIS)

Baumann, J.

1991-04-01

The thermodynamic computer models WATEQF, PHREEQE, EQ3NR/EQ6, and SOLMINEQ 88 have been verified for their applicability to describe geochemical processes in the system salt stock/cap rock/ground water, i.e. processes such as dissolution, sedimentation, exchange and redox reactions. To begin with, the hydrochemical data obtained by the hydrogeological survey at the Gorleben site have been evaluated to thus form a reference data base. Then, these data have been used to derive the essential conditions and benchmark data to establish a geochemical model. (HP) [de

Chemical elements in the environment: multi-element geochemical datasets from continental to national scale surveys on four continents

Science.gov (United States)

Caritat, Patrice de; Reimann, Clemens; Smith, David; Wang, Xueqiu

2017-01-01

During the last 10-20 years, Geological Surveys around the world have undertaken a major effort towards delivering fully harmonized and tightly quality-controlled low-density multi-element soil geochemical maps and datasets of vast regions including up to whole continents. Concentrations of between 45 and 60 elements commonly have been determined in a variety of different regolith types (e.g., sediment, soil). The multi-element datasets are published as complete geochemical atlases and made available to the general public. Several other geochemical datasets covering smaller areas but generally at a higher spatial density are also available. These datasets may, however, not be found by superficial internet-based searches because the elements are not mentioned individually either in the title or in the keyword lists of the original references. This publication attempts to increase the visibility and discoverability of these fundamental background datasets covering large areas up to whole continents.

Geochemical processes controlling the groundwater quality in lower ...

Indian Academy of Sciences (India)

of the study area is suitable for drinking and irrigation purposes except for few locations. 1. Introduction. Groundwater is ... agricultural purposes in most parts of the world. It ..... and Wastewater; 19th edn, APHA Washington DC. Arumugam K ...

Geochemical modelling. Pt.1, Pt.2

International Nuclear Information System (INIS)

Skytte Jensen, B.; Jensen, H.; Pearson, F.J.

1992-01-01

This work is carried out under cost-sharing contract with the European Atomic Energy Community in the framework of its fourth research programme on radioactive waste management and radioactive waste storage. This final report is subdivided into two parts. In the first part, JENSEN, a computer code for the computation of chemical equilibria in aqueous systems, describes the structure, function and use of a new geochemical computer program intended for PC's. The program, which is written in Turbo Pascal, version 4, is fundamentally similar to most other geochemical programs, but combines in one program several of the merits these programs have. The intention has been to make an advanced program, which also should be user friendly and fast, and to attain this several new algorithms have been developed and implemented. The program has a built-in database mainly based on the CHEMVAL compilation containing data for 395 soluble species and 149 minerals. The program can find equilibria in the presence of all or some of these soluble species, under conditions or fixed or floating pH and / or Redox potential. The program by itself eliminates a bad guess of a candidate for precipitation. In the present version, the program can identify which minerals and how much of them there will be formed when equilibrium is established. In the second part, LITTLE JOE, an expert system to support geochemical modelling, describes the construction of a minor expert system for use in the evaluation of analytical data for the composition of ground waters from limestone formation. Although the example given is rather limited in scope, the application of the expert system for the evaluation of the analytical data clearly demonstrates the mature expert knowledge imbedded in the system which is contrasted with the uncritical acceptance of analytical or theoretical data. With the overall neglect of ion-exchange and the formation of solid solutions in geochemical calculations, geochemistry is

Geochemical modelling of groundwater evolution using chemical equilibrium codes

International Nuclear Information System (INIS)

Pitkaenen, P.; Pirhonen, V.

1991-01-01

Geochemical equilibrium codes are a modern tool in studying interaction between groundwater and solid phases. The most common used programs and application subjects are shortly presented in this article. The main emphasis is laid on the approach method of using calculated results in evaluating groundwater evolution in hydrogeological system. At present in geochemical equilibrium modelling also kinetic as well as hydrologic constrains along a flow path are taken into consideration

Review of geochemical measurement techniques for a nuclear waste repository in bedded salt

International Nuclear Information System (INIS)

Knauss, K.G.; Steinborn, T.L.

1980-01-01

A broad, general review is presented of geochemical measurement techniques that can provide data necessary for site selection and repository effectiveness assessment for a radioactive waste repository in bedded salt. The available measurement techniques are organized according to the parameter measured. The list of geochemical parameters include all those measurable geochemical properties of a sample whole values determine the geochemical characteristics or behavior of the system. For each technique, remarks are made pertaining to the operating principles of the measurement instrument and the purpose for which the technique is used. Attention is drawn to areas where further research and development are needed

Hydrogeological and geochemical monitoring system for deep disposal in rock mass

International Nuclear Information System (INIS)

Itoh, K.; Otsuka, Y.; Ohi, Y.

1996-01-01

For investigation and construction of deep underground disposal site, it is very important to monitor three dimensional hydrogeological and geochemical condition for long term in all stages of investigation, construction and management. In deep geological disposal site, permeability of rock mass should be extremely lower than conventional civil engineering field, and natural piezometric pressure should be much higher than conventional groundwater monitoring in civil engineering. So, pressure measuring device should have wide measuring range and high precision especially for interference hydraulic test in investigation stage. And, simultaneous pressure measurement in plural points would be required for cost minimization. Recently, some kinds of multi-point pressure monitoring system has been presented. However, most of all system requires borehole with large diameter, and for utilization in plural boreholes, centralized sensor control is very difficult. And, in groundwater sampling for geochemical investigation, it is important to keep original chemical condition through sampling and transportation from sampling depth to surface. For these purposes, the authors have developed multi well multi point piezometric pressure measuring device, and groundwater sampling system for 1,000m depth. (author)

Geochemical Interactions and Viral-Prokaryote Relationships in Freshwater Environments

Science.gov (United States)

Kyle, J. E.; Ferris, G.

2009-05-01

Viral and prokaryotic abundances were surveyed throughout southern Ontario aquatic habitats to determine relationships with geochemical parameters in the natural environment. Surface water samples were collected from acid mine drainage in summer of 2007 and 2008 and from circum-neutral pH environments in October to November 2008. Site determination was based on collecting samples from various aquatic habitats (acid mine drainage, lakes, rivers, tributaries, wetlands) with differing bedrock geology (limestone and shale dominated vs granitic Canadian Shield) to obtain a range of geochemical conditions. At each site, measurements of temperature, pH, and Eh were conducted. Samples collected for microbial counts and electron imaging were preserved to a final concentration of 2.5 % (v/v) glutaraldehyde. Additional sample were filtered into 60 mL nalgene bottles and amber EPA certified 40 mL glass vials to determine chemical constituents and dissolved organic carbon (DOC), respectively. Water was also collected to determine additional physiochemical parameters (dissolved total iron, ferric iron, nitrate, sulfate, phosphate, alkalinity, and turbidity). All samples were stored at 4 °C until analysis. Viral and prokaryotic abundance was determined by staining samples with SYBR Green I and examining with a epifluorescence microscope under blue excitation. Multiple regression analysis using stepwise backwards regression and general linear models revealed that viral abundance was the most influential predictor of prokaryotic abundance. Additional predictors include pH, sulfate, phosphate, and magnesium. The strength of the model was very strong with 90 % of the variability explained (R2 = 0.90, p < 0.007). This is the first report, to our knowledge, of viruses exhibiting such strong controls over prokaryotic abundance in the natural environment. All relationships are positively correlated with the exception of Mg, which is negatively correlated. Iron was also noted as a

Uranium(VI) transport modeling: geochemical data and submodels

International Nuclear Information System (INIS)

Tripathi, V.S.

1984-01-01

Understanding the geochemical mobility of U(VI) and modeling its transport is important in several contexts including ore genesis, uranium exploration, nuclear and mill-tailings waste management, and solution mining of uranium ores. Adsorption is a major control on partitioning of solutes at the mineral/solution interface. The effect of carbonate, fluoride, and phosphate complexing on adsorption of uranium was investigated. A critical compilation of stability constants of inorganic complexes and solid compounds of U(VI) necessary for proper design of experiment and for modeling transport of uranium was prepared. The general features of U(VI) adsorption in ligand-free systems are similar to those characteristic of other hydrolyzable metal ions. The adsorption processes studied were found to be reversible. The adsorption model developed in ligand-free systems, when solution complexing is taken into account, proved remarkably successful in describing adsorption of uranium in the presence of carbonate and fluoride. The presence of phosphate caused a much smaller decrease in the extent of adsorption than expected; however, a critical reassessment of the stability of UO 2 2+ .HPO 4 2- complexes, showed that phosphato complexes, if any, are extremely weak under experimental conditions. Removal of uranium may have occurred due to precipitation of sodium uranyl phosphates in addition to adsorption

The evolution of the magmatic arc of Southern Peru (200-60 Ma), Arequipa area: insight from geochemical modeling

Science.gov (United States)

Demouy, S.; Benoit, M.; De Saint Blanquat, M.; Brunet, P.

2012-12-01

Cordilleran-type batholiths are built by prolonged arc activity along continental margins and may provide detailed magmatic records of the subduction system evolution. The magmas produced in subduction context involve both mantellic and crustal end members and are subject to various petrological processes. The MASH zones (Hildreth and Moorbath, 1988), at the basis of the continental crust, are the best places for the genesis of such hybrid magmas. The various geochemical signatures observed in the plutonic rocks, may also be attributed to source heterogeneities or generated by subsequent petrological processes. This study has focused in the Arequipa section of the Coastal Batholith of Southern Peru (200-60 Ma), in an area extending over 80x40 km. Major and trace elements as well as Sr and Nd isotopic analyses were performed in a set of 100 samples ranging from gabbro to granite. The obtained data highlight the wide heterogeneity of the geochemical signatures that is not related to the classification of the rocks. In first step, Rb/Sr systematic was used to isolate a set of samples plotting along a Paleocene isochron and defining a cogenetic suite. This suite appears to have evolved by simple fractional crystallization. By using reverse modeling, the parameters controlling the fractional crystallization process were defined, as partition coefficients, initial concentrations and amount of fractional crystallization. The other magmatic suites display a wide range of isotopic and geochemical signatures. To explain this heterogeneity, a model involving competition between fractional crystallization and magma mixing into MASH zones was proposed. A large range of hybrid magma types is potentially generated during the maturation of the system, but this range tends to disappear as fractionation and mixing occurs. Finally the model predicts the genesis of a homogeneous reservoir created at depth, from which magmas may evolve only by fractional crystallization. Therefore

Bayesian calibration of thermodynamic parameters for geochemical speciation modeling of cementitious materials

International Nuclear Information System (INIS)

Sarkar, S.; Kosson, D.S.; Mahadevan, S.; Meeussen, J.C.L.; Sloot, H. van der; Arnold, J.R.; Brown, K.G.

2012-01-01

Chemical equilibrium modeling of cementitious materials requires aqueous–solid equilibrium constants of the controlling mineral phases (K sp ) and the available concentrations of primary components. Inherent randomness of the input and model parameters, experimental measurement error, the assumptions and approximations required for numerical simulation, and inadequate knowledge of the chemical process contribute to uncertainty in model prediction. A numerical simulation framework is developed in this paper to assess uncertainty in K sp values used in geochemical speciation models. A Bayesian statistical method is used in combination with an efficient, adaptive Metropolis sampling technique to develop probability density functions for K sp values. One set of leaching experimental observations is used for calibration and another set is used for comparison to evaluate the applicability of the approach. The estimated probability distributions of K sp values can be used in Monte Carlo simulation to assess uncertainty in the behavior of aqueous–solid partitioning of constituents in cement-based materials.

Geochemical and modal data for igneous rocks associated with epithermal mineral deposits

Science.gov (United States)

du Bray, Edward A.

2014-01-01

The purposes of this report are to (1) present available geochemical and modal data for igneous rocks associated with epithermal mineral deposits and (2) to make those data widely and readily available for subsequent, more in-depth consideration and interpretation. Epithermal precious and base-metal deposits are commonly associated with subduction-related calc-alkaline to alkaline arc magmatism as well as back-arc continental rift magmatism. These deposits form in association with compositionally diverse extrusive and intrusive igneous rocks. Temperature and depth regimes prevailing during deposit formation are highly variable. The deposits form from hydrothermal fluids that range from acidic to near-neutral pH, and they occur in a variety of structural settings. The disparate temperature, pressure, fluid chemistry, and structural controls have resulted in deposits with wide ranging characteristics. Economic geologists have employed these characteristics to develop classification schemes for epithermal deposits and to constrain the important genetic processes responsible for their formation.

Geochemical controls on fluoriferous groundwaters of the Pliocene and the more recent aquifers: The case of Aigion region, Greece

Science.gov (United States)

Katsanou, K.; Siavalas, G.; Lambrakis, N.

2013-12-01

High fluoride concentrations (> 8 mg/L) in the groundwater of the Plio-Pleistocene sediments are rare; however, this is the case around Aigion town, where teeth fluorosis has been detected since the 80s. Aiming to investigate the origin and the mobility mechanism of fluorine in groundwater and sediments a hydrogeological and geochemical research has been conducted. The hydrogeological research revealed that the Na-HCO3 water type of boreholes aligned along a fault and hosted in the confined aquifers display the higher fluoride content. The unconfined aquifer is mostly dominated by Na-Ca-Mg-HCO3-SO4 water, which displays much lower fluoride concentrations. The most permeable sectors of this aquifer host fresh water of Ca-HCO3 type. The geochemical research revealed significant amount of fluorine in the base of a lignite sequence hosted in the Plio-Pleistocene sediments.

Processes of water rock interaction in the Turonian aquifer of Oum Er-Rabia Basin, Morocco

Science.gov (United States)

Ettazarini, Said

2005-12-01

Possible water rock interaction processes, in the Moroccan basin of Oum Er-Rabia, were discussed by a geochemical study of groundwater from the Turonian limestone aquifer, the most important water resource in the region. Different types of water according to the classification of Piper were defined. Waters have shown an evolution from dominant CHO3 Ca Mg type through mixed to SO4 Cl Ca Mg type. The use of geochemical diagrams and chemical speciation modeling method has shown that water rock interaction is mainly controlled by carbonate and anhydrite dissolution, ion exchange and reverse ion exchange processes. Water rock equilibrium conditions are favorable for the precipitation of calcite, dolomite, kaolinite and magnesian smectite.

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the northeastern Alaska Range, Healy, Mount Hayes, Nabesna, and Tanacross quadrangles, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 670 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the northeastern Alaska Range, in the Healy, Mount Hayes, Nabesna, and Tanacross quadrangles, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated into the statewide geochemical

Drowning in Geochemical Data: The Good, the bad, and the Ugly

Science.gov (United States)

Hofmann, A. W.; Goldstein, S. L.

2008-12-01

Geochemical databases are placing unprecedented amounts of geochemical data at the fingertips of professionals and students. How these data are being used is taking an increasingly important role in shaping our thinking about the Earth. Databases have helped to expose (and eventually kill?) some long- cherished myths, such as the idea of the well-homogenized upper-mantle reservoir, and and they have made geochemical data accessible to geophysicists and enabled them to look at geochemistry with fresh eyes, leading to genuinely new insights. Yet, their very accessibility also makes them "dangerous tools" in the hands of the inexperienced. Statistical treatment of masses of geochemical data without, or with excessive, filtering can yield all sorts of "answers" we would probably be better off without. Data that are severely flawed (due to alteration or poor analytical quality, errors in published data, or errors during data entry) might not be easily identified by, say, a geodynamicist. Other dangers stem from overrepresentation of over-sampled locations and the general, but faulty, assumption of random sampling of the Earth. We will show examples where raw downloads of data from databases without extensive screening can yield data collections where the garbage swamps the useful information. We will also show impressive but meaningless correlations, e.g. upper-mantle temperature versus atmospheric temperature. The lesson is that screening is necessary. On the other hand, sound database compilations now demonstrate that average incompatible-element concentrations in global MORB are two to five times higher than published estimates. This fundamentally changes 30-year-old geochemical mass balance estimates of the mantle. OIBs are fundamentally similar to MORBs but are isotopically shifted, on average, to more "enriched" values. Mantle geochemistry is now fully consistent with dynamic models of "whole-mantle" circulation, with the likely exception of a relatively small

Geomechanical/Geochemical Modeling Studies Conducted within the International DECOVALEX Project

International Nuclear Information System (INIS)

Birkholzer, J.T.; Rutqvist, J.; Sonnenthal, E.L.; Barr, D.; Chijimatsu, M.; Kolditz, O.; Liu, Q.; Oda, Y.; Wang, W.; Xie, M.; Zhang, C.

2005-01-01

The DECOVALEX project is an international cooperative project initiated by SKI, the Swedish Nuclear Power Inspectorate, with participation of about 10 international organizations. The general goal of this project is to encourage multidisciplinary interactive and cooperative research on modeling coupled thermo-hydro-mechanical-chemical (THMC) processes in geologic formations in support of the performance assessment for underground storage of radioactive waste. One of the research tasks, initiated in 2004 by the U.S. Department of Energy (DOE), addresses the long-term impact of geomechanical and geochemical processes on the flow conditions near waste emplacement tunnels. Within this task, four international research teams conduct predictive analysis of the coupled processes in two generic repositories, using multiple approaches and different computer codes. Below, we give an overview of the research task and report its current status

Geomechanical/Geochemical Modeling Studies Conducted Within the International DECOVALEX Project

International Nuclear Information System (INIS)

J.T. Birkholzer; J. Rutqvist; E.L. Sonnenthal; D. Barr; M.Chijimatsu; O. Kolditz; Q. Liu; Y. Oda; W. Wang; M. Xie; C. Zhang

2006-01-01

The DECOVALEX project is an international cooperative project initiated by SKI, the Swedish Nuclear Power Inspectorate, with participation of about 10 international organizations. The general goal of this project is to encourage multidisciplinary interactive and cooperative research on modeling coupled thermo-hydro-mechanical-chemical (THMC) processes in geologic formations in support of the performance assessment for underground storage of radioactive waste. One of the research tasks, initiated in 2004 by the U.S. Department of Energy (DOE), addresses the long-term impact of geomechanical and geochemical processes on the flow conditions near waste emplacement tunnels. Within this task, four international research teams conduct predictive analysis of the coupled processes in two generic repositories, using multiple approaches and different computer codes. Below, we give an overview of the research task and report its current status

Robot welding process control

Science.gov (United States)

Romine, Peter L.

1991-01-01

This final report documents the development and installation of software and hardware for Robotic Welding Process Control. Primary emphasis is on serial communications between the CYRO 750 robotic welder, Heurikon minicomputer running Hunter & Ready VRTX, and an IBM PC/AT, for offline programming and control and closed-loop welding control. The requirements for completion of the implementation of the Rocketdyne weld tracking control are discussed. The procedure for downloading programs from the Intergraph, over the network, is discussed. Conclusions are made on the results of this task, and recommendations are made for efficient implementation of communications, weld process control development, and advanced process control procedures using the Heurikon.

Time dynamics of background noise in geoelectrical and geochemical signals: An application in a seismic area of Southern Italy

International Nuclear Information System (INIS)

Di Bello, G.; Ragosta, M.; Heinicke, J.

1998-01-01

The paper analyses geoelectrical and geochemical time series jointly measured by means of a multi parametric automatic station close to an anomalous fluid emission in Val d'Agri (Basilicata, Italy). The investigated area is located on Southern Apennine chain that in past and recent years was interested by destructive earthquakes. After a complete pre-processing of time series, it analyses the fluctuations triggered by the seasonal cycles and focus the attention on the possible link between geo electrical and geochemical signals. In order to extract quantitative dynamical information from experimental time series, are detected scaling laws in power spectra that are typical fingerprints of fractional Brownian processes. After this analysis, the problem of the identification of extreme events in the time series has been approached. The paper considers significant anomalous patterns only when more consecutive values are above/below a fixed threshold in almost two of the time series jointly measured. The authors give the first preliminary results about the comparison between anomalous patterns detected in geo electrical and geochemical parameters and the local seismic activity and, finally, analyse the implications with the earthquake prediction problem

Thermo-hydro-geochemical modelling of the bentonite buffer. LOT A2 experiment

Energy Technology Data Exchange (ETDEWEB)

Sena, Clara; Salas, Joaquin; Arcos, David (Amphos 21 Consulting S.L., Barcelona (Spain))

2010-12-15

The Swedish Nuclear Fuel and waste management company (SKB) is conducting a series of long term buffer material (LOT) tests at the Aespoe Hard Rock Laboratory (HRL) to test the behaviour of the bentonite buffer under conditions similar to those expected in a KBS-3 deep geological repository for high level nuclear waste (HLNW). In the present work a numerical model is developed to simulate (i) the thermo-hydraulic, (ii) transport and (iii) geochemical processes that have been observed in the LOT A2 test parcel. The LOT A2 test lasted approximately 6 years, and consists of a 4 m long vertical borehole drilled in diorite rock, from the ground of the Aespoe HRL tunnel. The borehole is composed of a central heater, maintained at 130 deg C in the lower 2 m of the borehole, a copper tube surrounding the heater and a 100 mm thick ring of pre-compacted Wyoming MX-80 bentonite around the copper tube /Karnland et al. 2009/. The numerical model developed here is a 1D axis-symmetric model that simulates the water saturation of the bentonite under a constant thermal gradient; the transport of solutes; and, the geochemical reactions observed in the bentonite blocks. Two cases have been modelled, one considering the highest temperature reached by the bentonite (at 3 m depth in the borehole, where temperatures of 130 and 85 deg C have been recorded near the copper tube and near the granitic host rock, respectively) and the other case assuming a constant temperature of 25 deg C, representing the upper part of borehole, where the bentonite has not been heated. In the LOT A2 test, the initial partially saturated bentonite becomes progressively water saturated, due to the injection of Aespoe granitic groundwater at granite - bentonite interface. The transport of solutes during the bentonite water saturation stage is believed to be controlled by water uptake from the surrounding groundwater to the wetting front and, additionally, in the case of heated bentonite, by a cyclic evaporation

Thermo-hydro-geochemical modelling of the bentonite buffer. LOT A2 experiment

International Nuclear Information System (INIS)

Sena, Clara; Salas, Joaquin; Arcos, David

2010-12-01

The Swedish Nuclear Fuel and waste management company (SKB) is conducting a series of long term buffer material (LOT) tests at the Aespoe Hard Rock Laboratory (HRL) to test the behaviour of the bentonite buffer under conditions similar to those expected in a KBS-3 deep geological repository for high level nuclear waste (HLNW). In the present work a numerical model is developed to simulate (i) the thermo-hydraulic, (ii) transport and (iii) geochemical processes that have been observed in the LOT A2 test parcel. The LOT A2 test lasted approximately 6 years, and consists of a 4 m long vertical borehole drilled in diorite rock, from the ground of the Aespoe HRL tunnel. The borehole is composed of a central heater, maintained at 130 deg C in the lower 2 m of the borehole, a copper tube surrounding the heater and a 100 mm thick ring of pre-compacted Wyoming MX-80 bentonite around the copper tube /Karnland et al. 2009/. The numerical model developed here is a 1D axis-symmetric model that simulates the water saturation of the bentonite under a constant thermal gradient; the transport of solutes; and, the geochemical reactions observed in the bentonite blocks. Two cases have been modelled, one considering the highest temperature reached by the bentonite (at 3 m depth in the borehole, where temperatures of 130 and 85 deg C have been recorded near the copper tube and near the granitic host rock, respectively) and the other case assuming a constant temperature of 25 deg C, representing the upper part of borehole, where the bentonite has not been heated. In the LOT A2 test, the initial partially saturated bentonite becomes progressively water saturated, due to the injection of Aespoe granitic groundwater at granite - bentonite interface. The transport of solutes during the bentonite water saturation stage is believed to be controlled by water uptake from the surrounding groundwater to the wetting front and, additionally, in the case of heated bentonite, by a cyclic evaporation

Coupled Geochemical and Hydrological Processes Governing the Fate and Transport of Radionuclides and Toxic Metals Beneath the Hanford Tank Farms

International Nuclear Information System (INIS)

Scott Fendorf; Phil Jardine

2006-01-01

The goal of this research was to provide an improved understanding and predictive capability of coupled hydrological and geochemical mechanisms that are responsible for the accelerated migration and immobilization of radionuclides and toxic metals in the vadose zone beneath the Hanford Tank Farms

Factors controlling the geochemical evolution of fumarolic encrustations, Valley of Ten Thousand Smokes, Alaska

Science.gov (United States)

Kodosky, L.G.; Keith, T.E.C.

1993-01-01

Factor and canonical correlation analysis of geochemical data from eight fossil fumaroles suggest that six major factors controlled the formation and evolution of fumarolic encrustations on the 1912 ash-flow sheet in the Valley of Ten Thousand Smokes (VTTS). The six-factor solution model explains a large proportion (low of 74% for Ni to high of 99% for Si) of the individual element data variance. Although the primary fumarolic deposits have been degraded by secondary alteration reactions and up to 75 years of weathering, the relict encrustations still preserve a signature of vapor-phase element transport. This vapor-phase transport probably occurred as halide or oxyhalide species and was significant for As, Sb and Br. At least three, and possibly four, varied temperature leaching events affected the fumarolic deposits. High-temperature gases/liquids heavily altered the ejecta glass and mineral phases adjacent to the fumarolic conduit. As the fumaroles cooled. Fe-rich acidic condensate leached the ejecta and primary fumarolic deposits and resulted in the subsequent precipitation of Fe-hydroxides and/or Fe-oxides. Low- to ambient-temperature leaching and hydration reactions generated abundant hydrated amorphous phases. Up to 87% of the individual element data variance is apparently controlled by the chemistry of the ejecta on which the relict encrustations are found. This matrix chemistry factor illustrates that the primary fumarolic minerals surrounding the active VTTS vents observed by earlier workers have been effectively removed by the dissolution reactions. Element enrichment factors calculated for the VTTS relict encrustations support the statistical factor interpretations. On the average, the relict encrustations are enriched, relative to visibly unaltered matrix protolith, in As, Br, Cr, Sb, Cu, Ni, Pb, Fe, and LOI (an indirect measure of sample H2O content). ?? 1993.

The geochemical environment of nuclear fuel waste disposal

International Nuclear Information System (INIS)

Gascoyne, M.

1995-01-01

The concept for disposal of Canada's nuclear fuel waste in a geologic environment on the Canadian Shield has recently been presented by Atomic Energy of Canada Limited (AECL) to governments, scientists, and the public, for review. An important part of this concept concerns the geochemical environment of a disposal vault and includes consideration of rock and groundwater compositions, geochemical interactions between rocks, groundwaters, and emplaced vault materials, and the influences and significance of anthropogenic and microbiological effects following closure of the vault. This paper summarizes the disposal concept and examines aspects of the geochemical environment. The presence of saline groundwaters and reducing conditions at proposed vault depths (500-1000 m) in the Canadian Shield has an important bearing on the stability of the used nuclear fuel, its container, and buffer and backfill materials. The potential for introduction of anthropogenic contaminants and microbes during site investigations and vault excavation, operation, and sealing is described with examples from AECL's research areas on the Shield and in their underground research laboratory in southeastern Manitoba. (author)

Well sediments: a medium for geochemical prospecting, an example from the Nisa region, Portugal

NARCIS (Netherlands)

Vriend, S.P.; Dekkers, M.J.; Janssen, M.A.; Commandeur, J.

1991-01-01

Vriend, S.P., Dekkers, M.J.. Janssen, M.A. and Commandeur, J., 1991. Well sediments: a medium for geochemical prospecting, an example from the Nisa region. Portugal. In: A.W. Rose and P.M. Taufen I Editors). Geochemical Exploration ! 989. J. Geochem. Expior., 4 ! : ! 5 I- 167. Tile potential of

Geochemical and hydrologic factors controlling subsurface transport of poly- and perfluoroalkyl substances, Cape Cod, Massachusetts

Science.gov (United States)

Weber, Andrea K.; Barber, Larry B.; LeBlanc, Denis R.; Sunderland, Elsie M.; Vecitis, Chad D.

2017-01-01

Growing evidence that certain poly- and perfluoroalkyl substances (PFASs) are associated with negative human health effects prompted the U.S. Environmental Protection Agency to issue lifetime drinking water health advisories for perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) in 2016. Given that groundwater is a major source of drinking water, the main objective of this work was to investigate geochemical and hydrological processes governing the subsurface transport of PFASs at a former fire training area (FTA) on Cape Cod, Massachusetts, where PFAS-containing aqueous film-forming foams were used historically. A total of 148 groundwater samples and 4 sediment cores were collected along a 1200-m-long downgradient transect originating near the FTA and analyzed for PFAS content. The results indicate that unsaturated zones at the FTA and at hydraulically downgradient former domestic wastewater effluent infiltration beds both act as continuous PFAS sources to the groundwater despite 18 and 20 years of inactivity, respectively. Historically different PFAS sources are evident from contrasting PFAS composition near the water table below the FTA and wastewater-infiltration beds. Results from total oxidizable precursor assays conducted using groundwater samples collected throughout the plume suggest that some perfluoroalkyl acid precursors at this site are transporting with perfluoroalkyl acids.

Geochemical and physical drivers of microbial community structure in hot spring ecosystems

Science.gov (United States)

Havig, J. R.; Hamilton, T. L.; Boyd, E. S.; Meyer-Dombard, D. R.; Shock, E.

2012-12-01

Microbial communities in natural systems are typically characterized using samples collected from a single time point, thereby neglecting the temporal dynamics that characterize natural systems. The composition of these communities obtained from single point samples is then related to the geochemistry and physical parameters of the environment. Since most microbial life is adapted to a relatively narrow ecological niche (multiplicity of physical and chemical parameters that characterize a local habitat), these assessments provide only modest insight into the controls on community composition. Temporal variation in temperature or geochemical composition would be expected to add another dimension to the complexity of niche space available to support microbial diversity, with systems that experience greater variation supporting a greater biodiversity until a point where the variability is too extreme. . Hot springs often exhibit significant temporal variation, both in physical as well as chemical characteristics. This is a result of subsurface processes including boiling, phase separation, and differential mixing of liquid and vapor phase constituents. These characteristics of geothermal systems, which vary significantly over short periods of time, provide ideal natural laboratories for investigating how i) the extent of microbial community biodiversity and ii) the composition of those communities are shaped by temporal fluctuations in geochemistry. Geochemical and molecular samples were collected from 17 temporally variable hot springs across Yellowstone National Park, Wyoming. Temperature measurements using data-logging thermocouples, allowing accurate determination of temperature maximums, minimums, and ranges for each collection site, were collected in parallel, along with multiple geochemical characterizations as conditions varied. There were significant variations in temperature maxima (54.5 to 90.5°C), minima (12.5 to 82.5°C), and range (3.5 to 77.5°C) for

Constraining Lateral Evolution of Magmatic Behavior in North Tanzania from Geophysical and Geochemical Analyses

Science.gov (United States)

Gautier, S.; Tiberi, C.; Parat, F.; Baudouin, C.

2016-12-01

In the framework of CRAFTI and CoLiBrEA experiments in 2013, we proceeded to both seismic and geochemical studies along an EW profile through the North Tanzania Divergence. The data were collected along a line starting at the Ngorongoro volcanic area, ending at Kitumbeine edifice and crossing the rift valley. Recent seismological studies show lateral and depth variations for both velocity and Vp/Vs ratio within this area, particularly a change of Moho depth between the western and central parts of the rift. These two zones also exhibit diverse geochemical signatures that involve different magma storage (depth of reservoir, magma volume) and ascent as well as higher partial melts content for the western part. We take advantage of the recent and precise 3D lithospheric velocity models and receiver functions in this area to compare the structure and nature of Ngorongoro area and rift valley. We first compute ray path and establish regional coherency maps between piercing points, Vp/Vs ratio and tomographic images. Second, those results are compared with the composition of magma at depth obtained from a petrophysical and geochemical analysis of lava samples. We will discuss those results in terms of magmatic processes, and how they interact with the rifting in a cratonic lithosphere.

Instrumenting caves to collect hydrologic and geochemical data: case study from James Cave, Virginia

Science.gov (United States)

Schreiber, Madeline E.; Schwartz, Benjamin F.; Orndorff, William; Doctor, Daniel H.; Eagle, Sarah D.; Gerst, Jonathan D.

2015-01-01

Karst aquifers are productive groundwater systems, supplying approximately 25 % of the world’s drinking water. Sustainable use of this critical water supply requires information about rates of recharge to karst aquifers. The overall goal of this project is to collect long-term, high-resolution hydrologic and geochemical datasets at James Cave, Virginia, to evaluate the quantity and quality of recharge to the karst system. To achieve this goal, the cave has been instrumented for continuous (10-min interval) measurement of the (1) temperature and rate of precipitation; (2) temperature, specific conductance, and rate of epikarst dripwater; (3) temperature of the cave air; and (4) temperature, conductivity, and discharge of the cave stream. Instrumentation has also been installed to collect both composite and grab samples of precipitation, soil water, the cave stream, and dripwater for geochemical analysis. This chapter provides detailed information about the instrumentation, data processing, and data management; shows examples of collected datasets; and discusses recommendations for other researchers interested in hydrologic and geochemical monitoring of cave systems. Results from the research, briefly described here and discussed in more detail in other publications, document a strong seasonality of the start of the recharge season, the extent of the recharge season, and the geochemistry of recharge.

Interaction between shallow and deep aquifers in the Tivoli Plain (Central Italy) enhanced by groundwater extraction: A multi-isotope approach and geochemical modeling

International Nuclear Information System (INIS)

Carucci, Valentina; Petitta, Marco; Aravena, Ramon

2012-01-01

In the Tivoli Plain (Rome, Central Italy) the interaction between shallow and deep groundwater flow systems enhanced by groundwater extraction has been investigated using isotopic and chemical tracers. A conceptual model of the groundwater flowpaths has been developed and verified by geochemical modeling. A combined hydrogeochemical and isotopic investigation using ion relationships such as DIC/Cl − , Ca/(Ca + Mg)/SO 4 /(SO 4 + HCO 3 ), and environmental isotopes (δ 18 O, δ 2 H, 87 Sr/ 86 Sr, δ 34 S and δ 13 C) was carried out in order to determine the sources of recharge of the aquifer, the origin of solutes and the mixing processes in groundwater of Tivoli Plain. Multivariate statistical methods such as principal component analysis and Cluster analyses have confirmed the existence of different geochemical facies and the role of mixing in the chemical composition of the groundwater. Results indicate that the hydrochemistry of groundwater is characterized by mixing between end-members coming directly from carbonate recharge areas and to groundwater circulating in a deeply buried Meso-Cenozoic carbonate sequence. The travertine aquifer is fed by both flow systems, but a local contribution by direct input in the Plain has also been recognized. The stable isotope data ( 18 O, 2 H, 13 C and 34 S) supports the flow system conceptual model inferred from the geochemical data and represents key data to quantify the geochemical mixing in the different groundwaters of the Plain. The results of numerical modeling (PHREEQC) are consistent with the flowpaths derived from the hydrogeochemical conceptual model. The inverse models performed generated the main geochemical processes occurring in the groundwater flow system, which also included mixing. Geochemical and isotope modeling demonstrate an increasing influence of groundwater from the deeply buried aquifer in the travertine aquifer, enhanced by lowering of the travertine aquifer water table due to quarry pumping.

Kriging - a challenge in geochemical mapping

Czech Academy of Sciences Publication Activity Database

Štojdl, J.; Matys Grygar, Tomáš; Elznicová, J.; Popelka, J.; Váchová, T.; Hošek, Michal

2017-01-01

Roč. 19, APR (2017) ISSN 1607-7962. [EGU General Assembly 2017. 23.04.2017-28.04.2017, Vienna] Institutional support: RVO:61388980 Keywords : kriging * geochemical mapping Subject RIV: DD - Geochemistry http://meetingorganizer.copernicus.org/EGU2017/EGU2017-3615.pdf

Fracture Sealing in Shales: Geological and Geochemical Factors

International Nuclear Information System (INIS)

Cathelineau, Michel

2001-01-01

The so-called self-sealing processes can be re-examined at the light of geological and geochemical consideration about the past history of the rocks. The concept of 'self sealing' needs to consider the formation and the sealing of fractures, especially three main stages: (i) the initiation of the fracture (development of micro-cracks initiated from previous heterogeneities up to fracturing), ii) the fracturing processes which occur generally at depth in presence of a fluid phase, iii) the healing or sealing of the fractures which corresponds basically to two main processes: a restoration of the initial permeability of the rock block by reducing the transmissivity of the discontinuity down to values equivalent to that of the homogeneous medium before fracturing, or the sealing of the open discontinuity by precipitation of newly formed minerals. In the latter case, the evolution of the open fracture is driven by re-arrangement of particles or precipitation of newly formed material, either by dissolution/crystallisation processes or by crystallisation from the percolating fluids (advective processes). Such processes are governed by chemical processes, especially the rate of precipitation of minerals which depends of the degree of saturation with respect to the mineral, and the kinetics of precipitation. (author)

Opportunities and challenges for process control in process intensification

NARCIS (Netherlands)

Nikacevic, N.M.; Huesman, A.E.M.; Hof, Van den P.M.J.; Stankiewicz, A.

2012-01-01

This is a review and position article discussing the role and prospective for process control in process intensification. Firstly, the article outlines the classical role of control in process systems, presenting an overview of control systems’ development, from basic PID control to the advanced

Geochemical evidence for waning magmatism and polycyclic volcanism at Crater Flat, Nevada

International Nuclear Information System (INIS)

Perry, F.V.; Crowe, B.M.

1992-01-01

This paper reports that petrologic and geochemical studies of basaltic rocks in the Yucca Mountain region are currently focused on understanding the evolution of volcanism in the Crater Flat volcanic field and the mechanisms of polycyclic volcanic field and the mechanisms of polycyclic volcanism at the Lathrop Wells volcanic center, the youngest center in the Crater Flat volcanic field. Geochemical and petrologic data indicate that the magma chambers which supplied the volcanic centers at Crater Flat became situated at greater crustal depths as the field evolved. Deep magma chambers may be related to a waning magma flux that was unable to sustain upper crustal magma conduits and chambers. Geochemical data from the Lathrop Wells volcanic center indicate that eruptive units identified from field and geomorphic relationships are geochemically distinct. The geochemical variations cannot be explained by fractional crystallization of a single magma batch, indicating that several magma batches were involved in the formation of the Lathrop Wells center. Considering the low magma flux in the Yucca Mountain region in the Quaternary, the probability of several magma batches erupting essentially simultaneously at Lathrop Wells is considered remote

Process control using modern systems of information processing

International Nuclear Information System (INIS)

Baldeweg, F.

1984-01-01

Modern digital automation techniques allow the application of demanding types of process control. These types of process control are characterized by their belonging to higher levels in a multilevel model. Functional and technical aspects of the performance of digital automation plants are presented and explained. A modern automation system is described considering special procedures of process control (e.g. real time diagnosis)

Geochemical processes assessed by Rare Earth Elements fractionation at “Laguna Verde” acidic-sulphate crater lake (Azufral volcano, Colombia)

International Nuclear Information System (INIS)

Inguaggiato, Claudio; Burbano, Viviana; Rouwet, Dmitri; Garzón, Gustavo

2017-01-01

The geochemical behaviour of major elements, Fe, Al, Mn, and Rare Earth Elements (REE) was investigated in the “Laguna Verde” acidic crater lake of Azufral volcano (Colombia). The cold lake water (T close to 10 °C) is sulphate-dominated, due to absorption and oxidation of H_2S (pH 2.1–2.7, Eh 196–260 mV), and Na-enriched (Total Dissolved Solids 0.79 g L"−"1). The total amount of REE dissolved in the lake ranges from 3.3 to 9.1 ppb. The REE patterns normalized to the local rocks show a Light Rare Earth Elements (LREE) depletion quite constant in the 15 samples. Similar patterns were already found in the acidic sulphate springs of Nevado del Ruiz volcano-hydrothermal system, caused by the precipitation of alunite and jarosite, absorbing LREE and hence removing them from solution. Alunite and jarosite minerals are not oversaturated at chemical-physical conditions within the lake itself, but alunite becomes oversaturated for temperatures above ≈100 °C, reigning in the underlying hydrothermal system. Water temperatures close to 75 °C were found in the northern part of the lake. Coupling the distribution of REE in lake water (LREE depleted) and the saturation indexes, we suggest that the distribution of REE in the lake water is the result of the alunite precipitation in the northern part of the lake and/or in the deeper hydrothermal system. The acidic hydrothermal fluids mobilize the REE with contents up to ≈5 orders of magnitude higher than seawater; acidic-hydrothermal systems, such as acidic crater lakes, can hence be considered potential REE “reservoirs”. - Highlights: • Acidic crater lakes can be considered potential Rare Earth Elements reservoirs. • Alunite precipitation removes Light Rare Earth Elements. • Rare Earth Elements identify geochemical processes in volcano-hydrothermal systems.

Improved Geothermometry Through Multivariate Reaction-path Modeling and Evaluation of Geomicrobiological Influences on Geochemical Temperature Indicators: Final Report

Energy Technology Data Exchange (ETDEWEB)

Mattson, Earl [Idaho National Lab. (INL), Idaho Falls, ID (United States); Smith, Robert [Idaho National Lab. (INL), Idaho Falls, ID (United States); Fujita, Yoshiko [Idaho National Lab. (INL), Idaho Falls, ID (United States); McLing, Travis [Idaho National Lab. (INL), Idaho Falls, ID (United States); Neupane, Ghanashyam [Idaho National Lab. (INL), Idaho Falls, ID (United States); Palmer, Carl [Idaho National Lab. (INL), Idaho Falls, ID (United States); Reed, David [Idaho National Lab. (INL), Idaho Falls, ID (United States); Thompson, Vicki [Idaho National Lab. (INL), Idaho Falls, ID (United States)

2015-03-01

The project was aimed at demonstrating that the geothermometric predictions can be improved through the application of multi-element reaction path modeling that accounts for lithologic and tectonic settings, while also accounting for biological influences on geochemical temperature indicators. The limited utilization of chemical signatures by individual traditional geothermometer in the development of reservoir temperature estimates may have been constraining their reliability for evaluation of potential geothermal resources. This project, however, was intended to build a geothermometry tool which can integrate multi-component reaction path modeling with process-optimization capability that can be applied to dilute, low-temperature water samples to consistently predict reservoir temperature within ±30 °C. The project was also intended to evaluate the extent to which microbiological processes can modulate the geochemical signals in some thermal waters and influence the geothermometric predictions.

Overview of geochemical modeling needs for nuclear waste management

International Nuclear Information System (INIS)

Isherwood, D.; Wolery, T.

1984-01-01

Research needs include, but are not limited to: measurement of basic thermodynamic data at elevated temperatures for species identified by modelers as potentially important; evaluation of substances which control or limit precipitation and/or nucleation kinetics; sorption studies specifically designed to provide data needed for modeling. This includes the rate of sorption, desorption, and the characterization of the solid and aqueous phases; site-mixing models and thermodynamic data for secondary minerals that form solid solutions; the development of standard techniques for measuring rate laws for precipitation and dissolution kinetics; and measurement of rate laws describing redox kinetics, dissolution, and precipitation involving aqueous species and solid phases of interest to geochemical modelers

Geochemical behaviour of rare earths in Vitis vinifera grafted onto different rootstocks and growing on several soils

International Nuclear Information System (INIS)

Censi, P.; Saiano, F.; Pisciotta, A.; Tuzzolino, N.

2014-01-01

The geochemical behaviour of lanthanides and yttrium (Rare Earth Elements, REEs) has been investigated mainly in geological systems where these elements represent the best proxies of processes involving the occurrence of an interface between different media. This behaviour is assessed according to features recorded in sequences of REE concentrations along the REE series normalised with respect to a reference material. In this study, the geochemical behaviour of REE was investigated in different parts of Vitis vinifera specimens grown off-soil, on soils of different nature and grafted onto several rootstocks in order to evaluate effects induced by these changes. The results indicated that roots are the plant organs where REEs are preferentially concentrated, in particular elements from Sm to Ho (middle REE, MREE) whereas Eu enrichments occur in aerial parts. The geochemical behaviour of REE suggests that MREE enrichments in roots are due to preferential MREE interactions with biological membranes or to surface complexation with newly formed phosphates. Eu-positive anomalies suggest that Eu 3+ can form stable organic complexes in place of Ca 2+ in several biological processes in xylem fluids. The possibility that Eu mobility in these fluids can be enhanced by its reductive speciation as Eu 2+ cannot be ruled out. The assessment of the geochemical behaviour of REE according to the theory of the Tetrad Effect carried out confirms that REEs coming from soil are scavenged onto root tissues or mineral surfaces whereas their behaviour in aerial parts of V. vinifera is driven by dissolved complexation. - Highlights: • REE behaviour is driven by scavenging onto authigenic solids or membranes in roots. • REE behaviour is driven by dissolved complexation in aerial plant parts. • Positive Eu anomalies are a consequence of the REE translocation by xylem fluids. • Significant REE tetrad effects are observed in Vitis vinifera plants

Results of geochemical and mineralogical studies on uranium in Zechstein copper-bearing strata from Lubin-Polkowice area

International Nuclear Information System (INIS)

Bareja, E.

1977-01-01

The paper presents the results of geochemical and mineralogical studies on uranium in Zechstein copper-bearing strata from the Lubin-Polkowice area. It was found that particular lithofacial varietes of Zechstein copper-bearing strata are characterized by different concentration of uranium. The mineralogical studies made possible determination of the nature of uranium mineralization and the interdependence between uranium and lithology of copper-bearing strata. An interesting uranium mineralization was found in tectonic breccias which yield black blende and schroeckingerite as well as calcite, gypsum, pyrite, hematite and geothite. Secondary minerals such as schroeckingerite and geothite evidence intense weathering processes acting in the copper deposit. The highest value of geochemical background of uranium in the copper-bearing series is displayed by basel copper-bearing shales (so called pitch-black shales) - 68.10 x 10 -40 /0 U. Statistical distribution of that element is unimodal. Distribution of uranium is polymodal in basal sandstones of the copper-bearing series. The geochemical background of red-coloured sandstones (Rotliegendes) is low, equalling 0.39 x 10 40 /0 U, whilst that of gray-coloured sandstones (Zechstein) - 2.32 x 10 -40 /0 U. An anomallous population (344.0 x 10 -40 /0 U) found in the case of gray sandstones of the Lubin-Polkowice area evidences the effects of secondary processes on concentration of uranium. In sandstones occur black blende, carburanes as well as calcite, hematite and goethite. A bimodal distribution of uranium was found in carbonate series. Limestones are characterized by low value of geochemical background (Dsub(x1) = 0.78 x 10 -40 /0 U) whilst dolomites by markedly higher values of the background (Dsub(x2) = 2.73 x 10 -40 /0 U). (author)

Variations of Pb in a mine-impacted tropical river, Taxco, Mexico: Use of geochemical, isotopic and statistical tools

Energy Technology Data Exchange (ETDEWEB)

Arcega-Cabrera, F. [Unidad de Quimica en Sisal, Facultad de Quimica, UNAM, Sisal 97355 (Mexico)], E-mail: arcega@icmyl.unam.mx; Armienta, M.A. [Instituto de Geofisica, UNAM, Mexico 04510 (Mexico); Daessle, L.W. [Instituto de Investigaciones Oceanologicas, UABC, Ensenada 22870 (Mexico); Castillo-Blum, S.E. [Facultad de Quimica, UNAM, Mexico 04510 (Mexico); Talavera, O. [Escuela de Ciencias de la Tierra, UAG, Taxco Viejo 40201 (Mexico); Dotor, A. [Instituto de Geofisica, UNAM, Mexico 04510 (Mexico)

2009-01-15

The potential environmental threat from Pb in Mexican rivers impacted by historic mining activities was studied using geochemical, isotopic and statistical methods. Lead geochemical fractionation and factor analysis of fractionated and total Pb indicate that anthropogenic sources have contributed significantly to Pb concentrations, while natural sources have contributed only small amounts. The analyses also indicate that two main processes are controlling the total Pb variation throughout the year in both rivers: erosion with discharge processes, and proportional dilution related to differences in grain-size distribution processes. Bio-available Pb in riverbed sediments was greater than 50% in 80% of the sampling stations indicating a high potential environmental risk, according to the risk assessment criteria (RAC). Nevertheless, based on the environmental chemistry of Pb and on multivariate statistical analysis, these criteria did not apply in this particular case. Significant differences (p < 0.05) in total Pb concentrations (from 50 to 5820 mg kg{sup -1}) and in the geochemical fractionation were observed as a function of seasonality and location along the river flow path. In the Cacalotenango and Taxco rivers, the highest concentrations of total Pb were found at stations close to tailings during the rainy and post-rainy seasons. The geochemistry of Pb was mainly controlled, during the dry and post-rainy seasons by the organic matter and carbonate content, and in the rainy season by hydrological conditions (e.g., the increase in river flux), hydrological basin erosion, and the suspended solids concentration. Isotopic analyses of the {sup 210}Pb/{sup 214}Pb ratio showed three processes in the Cacalotenango and Taxco rivers. First, the accumulation of atmospheric excess {sup 210}Pb, favoured during calmer hydrodynamic conditions in the river basin commonly during dry periods, is recorded by a {sup 210}Pb/{sup 214}Pb ratio of >1. In the case of the Cacalotenango

Oak Ridge Geochemical Reconnaissance Program

International Nuclear Information System (INIS)

Arendt, J.W.

1977-03-01

The Oak Ridge reconnaissance program is responsible for the geochemical survey in a 12-state area covering Texas, Oklahoma, Kansas, Nebraska, South Dakota, North Dakota, Minnesota, Wisconsin, Michigan, Iowa, Indiana, and Illinois as part of the National Uranium Resource Evaluation Program. The program concept is outlined and the planning and organization of the program is discussed

Process control program development

International Nuclear Information System (INIS)

Dameron, H.J.

1985-01-01

This paper details the development and implementation of a ''Process Control Program'' at Duke Power's three nuclear stations - Oconee, McGuire, and Catawba. Each station is required by Technical Specification to have a ''Process Control Program'' (PCP) to control all dewatering and/or solidification activities for radioactive wastes

Chemical process control using Mat lab

International Nuclear Information System (INIS)

Kang, Sin Chun; Kim, Raeh Yeon; Kim, Yang Su; Oh, Min; Yeo, Yeong Gu; Jung, Yeon Su

2001-07-01

This book is about chemical process control, which includes the basis of process control with conception, function, composition of system and summary, change of laplace and linearization, modeling of chemical process, transfer function and block diagram, the first dynamic property of process, the second dynamic property of process, the dynamic property of combined process, control structure of feedback on component of control system, the dynamic property of feedback control loop, stability of closed loop control structure, expression of process, modification and composition of controller, analysis of vibration response and adjustment controller using vibration response.

Initial geochemical characteristics of fluid fine tailings in an oil sands end pit lake

Energy Technology Data Exchange (ETDEWEB)

Dompierre, Kathryn A. [Department of Civil and Geological Engineering, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5A9 (Canada); Lindsay, Matthew B.J., E-mail: matt.lindsay@usask.ca [Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5E2 (Canada); Cruz-Hernández, Pablo [Department of Geology, University of Huelva, Campus ‘El Carmen’, E-21071 Huelva (Spain); Halferdahl, Geoffrey M. [Environmental Research and Development, Syncrude Canada Limited, Edmonton, Alberta T6N 1H4 (Canada)

2016-06-15

Geochemical characteristics of fluid fine tailings (FFT) were examined in Base Mine Lake (BML), which is the first full-scale demonstration oil sands end pit lake (EPL) in northern Alberta, Canada. Approximately 186 Mm{sup 3} of FFT was deposited between 1994 and 2012, before BML was established on December 31, 2012. Bulk FFT samples (n = 588) were collected in July and August 2013 at various depths at 15 sampling sites. Temperature, solid content, electrical conductivity (EC), pH, Eh and alkalinity were measured for all samples. Detailed geochemical analyses were performed on a subset of samples (n = 284). Pore-water pH decreased with depth by approximately 0.5 within the upper 10 m of the FFT. Major pore-water constituents included Na (880 ± 96 mg L{sup −1}) and Cl (560 ± 95 mg L{sup −1}); Ca (19 ± 4.1 mg L{sup −1}), Mg (11 ± 2.0 mg L{sup −1}), K (16 ± 2.3 mg L{sup −1}) and NH{sub 3} (9.9 ± 4.7 mg L{sup −1}) were consistently observed. Iron and Mn concentrations were low within FFT pore water, whereas SO{sub 4} concentrations decreased sharply across the FFT–water interface. Geochemical modeling indicated that FeS{sub (s)} precipitation was favoured under SO{sub 4}-reducing conditions. Pore water was also under-saturated with respect to gypsum [CaSO{sub 4}·2H{sub 2}O], and near saturation with respect to calcite [CaCO{sub 3}], dolomite [CaMg(CO{sub 3}){sub 2}] and siderite [FeCO{sub 3}]. X-ray diffraction (XRD) suggested that carbonate-mineral dissolution largely depleted calcite and dolomite. X-ray absorption near edge structure (XANES) spectroscopy revealed the presence of FeS{sub (s)}, pyrite [FeS{sub 2}], and siderite. Carbonate-mineral dissolution and secondary mineral precipitation have likely contributed to FFT dewatering and settlement. However, the long-term importance of these processes within EPLs remains unknown. These results provide a reference for assessing the long-term geochemical evolution of oil sands EPLs, and offer

DUAL-PROCESS, a highly reliable process control system

International Nuclear Information System (INIS)

Buerger, L.; Gossanyi, A.; Parkanyi, T.; Szabo, G.; Vegh, E.

1983-02-01

A multiprocessor process control system is described. During its development the reliability was the most important aspect because it is used in the computerized control of a 5 MW research reactor. DUAL-PROCESS is fully compatible with the earlier single processor control system PROCESS-24K. The paper deals in detail with the communication, synchronization, error detection and error recovery problems of the operating system. (author)

Geochemical signature of columbite-tantalite and radiometric survey of radioactive pegmatites in the region of Parelhas, Rio Grande do Norte, Brazil

International Nuclear Information System (INIS)

Moura, Jorge Costa de

2013-01-01

This thesis is the result of geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area, located in the surroundings of the city of Parelhas in the region of the Serra da Borborema, is well known for its thousands of pegmatitic bodies exploited in primitive mines called 'garimpos'. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of the ratio U/Th versus Nb 2 O 5 /Ta 2 O 5 provides geochemical signatures (analytical fingerprints) for the source location of such ore. A test of the new method with coltan samples of commercial batches from the Brazilian states Amapa and Rondonia also generated distinct geochemical signatures. A radiometric survey (CPS) was carried out in several mines and pegmatites to study the environmental impact of gamma radiation. It included in situ measurements of pegmatite walls, host rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and environmental gamma radiation therefore generally is not enhanced to a dangerous level. (author)

A stream sediment geochemical survey of the Ganga River headwaters in the Garhwal Himalaya

Science.gov (United States)

Mukherjee, P.K.; Purohit, K.K.; Saini, N.K.; Khanna, P.P.; Rathi, M.S.; Grosz, A.E.

2007-01-01

This study models geochemical and adjunct geologic data to define provinces that are favorable for radioactive-mineral exploration. A multi-element bed-sediment geochemical survey of streams was carried out in the headwaters region of the Ganga River in northern India. Overall median values for uranium and thorium (3.6 and 13.8 ppm; maxima of 4.8 and 19.0 ppm and minima of 3.1 and 12.3 ppm respectively) exceed average upper crustal abundances (2.8 and 10.7 ppm) for these radioactive elements. Anomalously high values reach up to 8.3 and 30.1 ppm in thrust zone rocks, and 11.4 and 22.5 ppm in porphyroids. At their maxima, these abundances are nearly four- and three-fold (respectively) enriched in comparison to average crustal abundances for these rock types. Deformed, metamorphosed and sheared rocks are characteristic of the main central thrust zone (MCTZ). These intensively mylonitized rocks override and juxtapose porphyritic (PH) and proterozoic metasedimentary rock sequences (PMS) to the south. Granitoid rocks, the major protoliths for mylonites, as well as metamorphosed rocks in the MCT zone are naturally enriched in radioelements; high values associated with sheared and mylonitized zones are coincident with reports of radioelement mineralization and with anomalous radon concentrations in soils. The radioelement abundance as well as REE abundance shows a northward enrichment trend consistent with increasing grade of metamorphism indicating deformation-induced remobilization of these elements. U and Th illustrate good correlation with REEs but not with Zr. This implies that zircon is not a principal carrier of U and Th within the granitoid-dominant thrust zone and that other radioelement-rich secondary minerals are present in considerable amounts. Thus, the relatively flat, less fractionated, HREE trend is also not entirely controlled by zircon. The spatial correlation of geologic boundary zones (faults, sheared zones) with geochemical and with geophysical (Rn

Process control for sheet-metal stamping process modeling, controller design and shop-floor implementation

CERN Document Server

Lim, Yongseob; Ulsoy, A Galip

2014-01-01

Process Control for Sheet-Metal Stamping presents a comprehensive and structured approach to the design and implementation of controllers for the sheet metal stamping process. The use of process control for sheet-metal stamping greatly reduces defects in deep-drawn parts and can also yield large material savings from reduced scrap. Sheet-metal forming is a complex process and most often characterized by partial differential equations that are numerically solved using finite-element techniques. In this book, twenty years of academic research are reviewed and the resulting technology transitioned to the industrial environment. The sheet-metal stamping process is modeled in a manner suitable for multiple-input multiple-output control system design, with commercially available sensors and actuators. These models are then used to design adaptive controllers and real-time controller implementation is discussed. Finally, experimental results from actual shopfloor deployment are presented along with ideas for further...

Evaluation of geochemical properties used in area-to-location screening for a nuclear waste repository at the Nevada Test Site

International Nuclear Information System (INIS)

Purson, J.D.

1983-03-01

The area-to-location screening of a potential site for a nuclear waste repository is dependent on geologic compatibility. Specifically, the geochemical properties of candidate locations are significant in the overall site evaluation. This report describes three geochemical factors or attributes and their application to an area-to-location screening of the southwestern quadrant of the Nevada Test Site and contiguous areas. These are only 3 of 31 attributes examined in the screening process. Geochemical and rock media considerations relevant to site screening include: (1) retardation by hydraulics - a study of ground-water movement through fractures vs a permeable matrix; (2) thermal stability of minerals - a measurement of undesirable mineral assemblages in the rock; and (3) retardation by sorption - an evaluation of the total sorptive capacity at a location, based on stratigraphy and lithology. Twelve potential host rocks situated in 20 locations are examined; 2 of these have consistently fewer favorable characteristics, and 6 others have generally fewer favorable characteristics than the 4 remaining rock units. The four units that appear most favorable by geochemical measures are the tuffaceous beds of Calico Hills, granite intrusives, the densely welded Topopah Spring tuff, and the Crater Flat Tuff at Yucca Mountain

Geochemical orientation for mineral exploration in the Hashemite Kingdom of Jordan

Science.gov (United States)

Overstreet, W.C.; Grimes, D.J.; Seitz, J.F.

1982-01-01

This report is a supplement to previous accounts of geochemical exploration conducted in the Hashemite Kingdom of Jordan by the Natural Resources Authority of the Royal Government of Jordan and the U.S. Geological Survey. The field work on which this report is based was sponsored by the U.S. Agency for International Development, U.S. Department of State. Procedures used in collecting various kinds of rocks, ores, slags, eluvial and alluvial sediments, heavy-mineral concentrates, and organic materials for use as geochemical sample media are summarized, as are the laboratory procedures followed for the analysis of these sample materials by semiquantitative spectrographic, atomic absorption, fluorometric, and X-ray diffraction methods. Geochemical evaluations of the possibilities for economic mineral deposits in certain areas are presented. The results of these preliminary investigations open concepts for further use in geochemical exploration in the search for metallic mineral deposits in Jordan. Perhaps the most desirable new activity would be hydrogeochemical exploration for uranium and base metals, accompanied by interpretation of such remote-sensing data as results of airborne radiometric surveys and computer-enhanced LANDSAT imagery. For more conventional approaches to geochemical exploration, however, several fundamental problems regarding proper choice of geochemical sample media for different geologic and geographic parts of the Country must be solved before effective surveys can be made. The present results also show that such common geochemical exploration techniques as the determination of the trace-element contents of soils, plant ash, and slags have direct application also toward the resolution of several archaeological problems in Jordan. These include the relation of trace-elements chemistry of local soils to the composition of botanic remains, the trace-elements composition of slags to the technological development of the extractive metallurgy of

Geochemical methods for identification of formations being prospective for uranium

International Nuclear Information System (INIS)

Zhukova, A.M.; Komarova, N.I.; Spiridonov, A.A.; Shor, G.M.

1985-01-01

Geochemical methods of uranium content evaluation in metamorphic, ultrametamorphic and sedimentary formations are considered. At that, the following four factors are of the highest importance: 1) average uranium content-geochemical background; 2) character of uranium distribution; 3) forms of uranium presence; 4) the value of thorium-uranium ratio. A complex of radiogeochemical criteria, favourable for uranium presence is formulated: high average background content of total and '' mobile''uranium and high value of variation coefficient (80-100% and above); low (approximately one or lower) thorium-uranium ratio; sharp increase in uranium concentration in accessory minerals. Radiogeochemical peculiarities of metamorphic and ultrametamorphic formations prospective for uranium are enumerated. The peculiarities condition specificity of geochemical prospecting methods. Prospecting methods first of all must be directed at the evaluation of radioelement distribution parameters and specification of the forms of their presence

Geochemical Implications of CO2 Leakage Associated with Geologic Storage: A Review

Energy Technology Data Exchange (ETDEWEB)

Harvey, Omar R.; Qafoku, Nikolla; Cantrell, Kirk J.; Brown, Christopher F.

2012-07-09

Leakage from deep storage reservoirs is a major risk factor associated with geologic sequestration of carbon dioxide (CO2). Different scientific theories exist concerning the potential implications of such leakage for near-surface environments. The authors of this report reviewed the current literature on how CO2 leakage (from storage reservoirs) would likely impact the geochemistry of near surface environments such as potable water aquifers and the vadose zone. Experimental and modeling studies highlighted the potential for both beneficial (e.g., CO2 re sequestration or contaminant immobilization) and deleterious (e.g., contaminant mobilization) consequences of CO2 intrusion in these systems. Current knowledge gaps, including the role of CO2-induced changes in redox conditions, the influence of CO2 influx rate, gas composition, organic matter content and microorganisms are discussed in terms of their potential influence on pertinent geochemical processes and the potential for beneficial or deleterious outcomes. Geochemical modeling was used to systematically highlight why closing these knowledge gaps are pivotal. A framework for studying and assessing consequences associated with each factor is also presented in Section 5.6.

Semi-detailed uranium geochemical survey in Northwestern Samar (27 March 1979 - 4 July 1979)

International Nuclear Information System (INIS)

Santos, G. Jr.; Ogena, M.; Tauli, G.

1980-04-01

A uranium geochemical survey was conducted to delineate in detail the uranium prospective area(s) in northwestern Samar. A total of 805 stream sediments and 1.115 water samples were obtained from the target areas from uranium analysis. Geochemical anomalies were indicated in San Isidro and Mauo. Geochemical correlations between uranium and trace elements (Pb, Ag, Ni, Cu, Co, Zn and Mn) were generally poor. (ELC)

Synthesizing Earth's geochemical data for hydrogeochemical analysis

Science.gov (United States)

Brantley, S. L.; Kubicki, J.; Miller, D.; Richter, D.; Giles, L.; Mitra, P.

2007-12-01

For over 200 years, geochemical, microbiological, and chemical data have been collected to describe the evolution of the surface earth. Many of these measurements are data showing variations in time or in space. To forward predict hydrologic response to changing tectonic, climatic, or anthropogenic forcings requires synthesis of these data and utilization in hydrogeochemical models. Increasingly, scientists are attempting to synthesize such data in order to make predictions for new regions or for future time periods. However, to make such complex geochemical data accessible requires development of sophisticated cyberinfrastructures that both invite uploading as well as usage of data. Two such cyberinfrastructure (CI) initiatives are currently developing, one to invite and promote the use of environmental kinetics data (laboratory time course data) through ChemxSeer, and the other to invite and promote the use of spatially indexed geochemical data for the Earth's Critical Zone through CZEN.org. The vision of these CI initiatives is to provide cyber-enhanced portals that encourage domain scientists to upload their data before publication (in private cyberspace), and to make these data eventually publicly accessible (after an embargo period). If the CI can be made to provide services to the domain specialist - e.g. to provide data analysis services or data comparison services - we envision that scientists will upload data. In addition, the CI can promote the use and comparison of datasets across disciplines. For example, the CI can facilitate the use of spatially indexed geochemical data by scientists more accustomed to dealing with time-course data for hydrologic flow, and can provide user-friendly interfaces with CI established to facilitate the use of hydrologic data. Examples of the usage of synthesized data to predict soil development over the last 13ky and its effects on active hydrological flow boundaries in surficial systems will be discussed for i) a N

Geochemical fingerprints and pebbles zircon geochronology

Indian Academy of Sciences (India)

Home; Journals; Journal of Earth System Science; Volume 125; Issue 7. Geochemical fingerprints and pebbles zircon geochronology: Implications for the provenance and tectonic setting of Lower Cretaceous sediments in the Zhucheng Basin (Jiaodong peninsula, North China). Jin-Long Ni Jun-Lai Liu Xiao-Ling Tang ...

Geochemical, hydrological, and biological cycling of energy residual. Research plan

International Nuclear Information System (INIS)

Wobber, F.J.

1983-03-01

Proposed research goals and specific research areas designed to provide a base of fundamental scientific information so that the geochemical, hydrological, and biophysical mechanisms that contribute to the transport and long term fate of energy residuals in natural systems can be understood are described. Energy development and production have resulted in a need for advanced scientific information on the geochemical transformations, transport rates, and potential for bioaccumulation of contaminants in subsurface environments

Geology, alteration, mineralization and geochemical study in Kalateh Taimour area, NE Iran

Directory of Open Access Journals (Sweden)

Zahra Alaminia

2010-11-01

Full Text Available The area is located 20 km northwest of Kashmar and about 4 km of Kalateh Taimour in Khorasan Razavi province. The study area is part of Tertiary volcanic-plutonic belt north of Daruneh fault and its situation in tectonic inliers between two important active faults, Doruneh and Taknar. Volcanic rocks are mainly intermediate to acid pyroclastic type. They formed during early Tertiary. The volcanic rocks of the Kalateh Taimour area are predominantly andesitic basalt, andesite, latite, trachyte, dacite and rhyodacite and are observed as lava, tuff, lapilli tuff and agglomerate. Field evidences and study show several subvolcanic bodies including quartz hornblende biotite monzodiorite porphyry, quartz biotite monzodiorite porphyry, quartz diorite porphyry and microdiorite which are intruded sometime in mid-Tertiary. In this belt, new methods of image processing were used for enhancing the alteration zones to help near infra red and short wavelength infrared and bands example band ratios and principle component method. Propylitic, sericitic and argillic are the main alteration types. Minor silicification is found in some areas. Alteration is extent but mineralization is limited. Mineralization is mainly controlled by fault system. Several mineralized faults are being discovered. Open space filling features are abundant. In the study area, disseminate and stock work mineralization are abundant. The amount of sulfide minerals is very small. Ancient mining is present in the area. Stream sediment geochemical study shows a very broad and high level of gold anomaly. Rock geochemical study show very high levels of Au, Ag, Cu, Pb, Zn and Au value is correlative to Cu, Pb, Zn and Ag values. Due to alteration modeling, non uniformity in mineralization and low abundance of sulfide mineralization suggest study in low sulphidation Au-Cu deposit.

Factors controlling the regional distribution of vanadium in ground water

Science.gov (United States)

Wright, Michael T.; Belitz, Kenneth

2010-01-01

Although the ingestion of vanadium (V) in drinking water may have possible adverse health effects, there have been relatively few studies of V in groundwater. Given the importance of groundwater as a source of drinking water in many areas of the world, this study examines the potential sources and geochemical processes that control the distribution of V in groundwater on a regional scale. Potential sources of V to groundwater include dissolution of V rich rocks, and waste streams from industrial processes. Geochemical processes such as adsorption/desorption, precipitation/dissolution, and chemical transformations control V concentrations in groundwater. Based on thermodynamic data and laboratory studies, V concentrations are expected to be highest in samples collected from oxic and alkaline groundwater. However, the extent to which thermodynamic data and laboratory results apply to the actual distribution of V in groundwater is not well understood. More than 8400 groundwater samples collected in California were used in this study. Of these samples, high (> or = 50 μg/L) and moderate (25 to 49 μg/L) V concentrations were most frequently detected in regions where both source rock and favorable geochemical conditions occurred. The distribution of V concentrations in groundwater samples suggests that significant sources of V are mafic and andesitic rock. Anthropogenic activities do not appear to be a significant contributor of V to groundwater in this study. High V concentrations in groundwater samples analyzed in this study were almost always associated with oxic and alkaline groundwater conditions, which is consistent with predictions based on thermodynamic data.

Research on the hydrogeological and geochemical conditions at the coastal area and submarine formations

International Nuclear Information System (INIS)

Tokunaga, Tomochika; Taniguchi, Makoto; Goto, Junji

2003-05-01

One of the major concerns for the high-level radioactive waste disposal is the possibility of the radionuclides to reach biosphere by groundwater flow. Recent research results have shown that the fresh groundwater discharge from subsea formations are widespread phenomena, thus, it is necessary to evaluate the submarine groundwater discharge as possible pathways of contaminant discharge towards the biosphere. It is also important to unravel the groundwater flow and associated material transport at the coastal area and subsea formations. To better understand the groundwater flow processes and the submarine groundwater discharge, we have conducted the hydrological, hydrogeological, geochemical, and numerical modeling studies at the Kurobe alluvial fan and its offshore, Toyama Prefecture, Japan. In this report, the results of the following research activities are presented: 1) Development and application of a method to detect the locations of the submarine groundwater discharge. 2) Development and application of a method to collect uncontaminated groundwater samples from subsea formations. 3) Measurements of submarine groundwater discharge fluxes by automated seepage meter. 4) Hydrological and geochemical studies for groundwater flow at the coastal area. 5) Geochemical studies to understand sources of fresh submarine groundwater discharge. 6) Examination of groundwater flow and submarine groundwater discharge using methane concentration and carbon isotope ratio. 7) Numerical modeling studies for coastal groundwater flow system. (author)

Geochemical modelling of CO2-water-rock interactions for carbon storage : data requirements and outputs

International Nuclear Information System (INIS)

Kirste, D.

2008-01-01

A geochemical model was used to predict the short-term and long-term behaviour of carbon dioxide (CO 2 ), formation water, and reservoir mineralogy at a carbon sequestration site. Data requirements for the geochemical model included detailed mineral petrography; formation water chemistry; thermodynamic and kinetic data for mineral phases; and rock and reservoir physical characteristics. The model was used to determine the types of outputs expected for potential CO 2 storage sites and natural analogues. Reaction path modelling was conducted to determine the total reactivity or CO 2 storage capability of the rock by applying static equilibrium and kinetic simulations. Potential product phases were identified using the modelling technique, which also enabled the identification of the chemical evolution of the system. Results of the modelling study demonstrated that changes in porosity and permeability over time should be considered during the site selection process.

Archean crust-mantle geochemical differentiation

Science.gov (United States)

Tilton, G. R.

Isotope measurements on carbonatite complexes and komatiites can provide information on the geochemical character and geochemical evolution of the mantle, including the sub-continental mantle. Measurements on young samples establish the validity of the method. These are based on Sr, Nd and Pb data from the Tertiary-Mesozoic Gorgona komatiite and Sr and Pb data from the Cretaceous Oka carbonatite complex. In both cases the data describe a LIL element-depleted source similar to that observed presently in MORB. Carbonatite data have been used to study the mantle beneath the Superior Province of the Canadian Shield one billion years (1 AE) ago. The framework for this investigation was established by Bell et al., who showed that large areas of the province appear to be underlain by LIL element-depleted mantle (Sr-85/Sr-86=0.7028) at 1 AE ago. Additionally Bell et al. found four complexes to have higher initial Sr ratios (Sr-87/Sr-86=0.7038), which they correlated with less depleted (bulk earth?) mantle sources, or possibly crustal contamination. Pb isotope relationships in four of the complexes have been studied by Bell et al.

Archean crust-mantle geochemical differentiation

Science.gov (United States)

Tilton, G. R.

1983-01-01

Isotope measurements on carbonatite complexes and komatiites can provide information on the geochemical character and geochemical evolution of the mantle, including the sub-continental mantle. Measurements on young samples establish the validity of the method. These are based on Sr, Nd and Pb data from the Tertiary-Mesozoic Gorgona komatiite and Sr and Pb data from the Cretaceous Oka carbonatite complex. In both cases the data describe a LIL element-depleted source similar to that observed presently in MORB. Carbonatite data have been used to study the mantle beneath the Superior Province of the Canadian Shield one billion years (1 AE) ago. The framework for this investigation was established by Bell et al., who showed that large areas of the province appear to be underlain by LIL element-depleted mantle (Sr-85/Sr-86=0.7028) at 1 AE ago. Additionally Bell et al. found four complexes to have higher initial Sr ratios (Sr-87/Sr-86=0.7038), which they correlated with less depleted (bulk earth?) mantle sources, or possibly crustal contamination. Pb isotope relationships in four of the complexes have been studied by Bell et al.

Geochemical signature of columbite-tantalite and environmental impact of radioactive pegmatite mining in the Parelhas region, Rio Grande do Norte, Northeast Brazil

International Nuclear Information System (INIS)

Moura, Jorge Costa de; Cruz, Paulo R.; Pereira, Valmir; Ludka, Isabel P.; Mendes, Julio C.

2013-01-01

This article comprises geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area is located in the surroundings of the city of Parelhas, in the geotectonic Province of Borborema. It is well known for its thousands of pegmatitic bodies exploited in primitive mines called garimpos. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of U/Th vs. Nb 2 O 5 /Ta 2 O 5 provides geochemical signatures (analytical fingerprints) for the source location of such ore. The new method was tested with coltan samples of commercial batches from the Brazilian states of Amapa and Rondonia and also generated distinct geochemical signatures. A radiometric survey (CPS) to study the environmental impact of gamma radiation was also carried out in several mines and pegmatites. It included in situ measurements of pegmatite walls, enclosing rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and therefore environmental gamma radiation generally is not enhanced to a dangerous level. (author)

Chemical and geochemical studies off the coast of Washington. Progress report, September 1980-July 1981

International Nuclear Information System (INIS)

Carpenter, R.

1981-07-01

This report summarizes progress from September 1980 through July 1981 on a series of marine chemical and geochemical investigations involving both laboratory studies and field studies off the coast of Washington. Most of the field work has been on the Washington continental shelf, slope, and the submarine canyons indenting the shelf north of the Columbia River. The aim is to provide basic data required to characterize underlying chemical and physical processes and their rates which control the distributions, concentrations, and ultimate fate of some of the potentially hazardous agents associated with fossil fuel and/or nuclear power production or transportation. We are concentrating on several processes which we feel are of special importance in the sea, and developing methodologies and expertise to study them. Laboratory and field experiments and theories derived from them are being used iteratively to investigate: (1) vertical transfer of trace chemicals from surface seawaters to underlying waters and sediments; (2) processes which may transfer certain chemicals from sediments back into the overlying water column; (3) redox processes which besides changing valence states of certain chemicals may alter their precipitation/dissolution tendencies, their biological availability and/or toxicity; and (4) accumulation histories of potentially hazardous chemicals in sediments during the past 100 years

Acceptance of the 2014 Geochemical Society Distinguished Service Award by Carla Koretsky

Science.gov (United States)

Koretsky, Carla

2015-06-01

I am deeply touched to have received the Geochemical Society Distinguished Service Award. It was a great surprise when I received the notice that I had been chosen for the award. It has been a tremendous pleasure to work on behalf of student members of the Geochemical Society, Japanese Geochemical Society and the European Association of Geochemists to organize the student travel grants over the past few years. Certainly, this is not an effort that I undertook on my own. Many, many members of the GS, the JGS and the EAG generously donated their time and expertise to serve as reviewers for the many travel grant applicants we receive each year. Seth Davis, the GS Chief Operating Officer, spent countless hours helping to organize applications, the website, distribution of funds and many other aspects of the competition. Without Seth and the many expert reviewers, we could not run the travel grant program each year and provide this important financial support to allow more students to experience the Goldschmidt Conference. I also enjoyed my time as Geochemical News co-editor, and I should point out that GN during those years was ably co-edited by Johnson Haas. It has been a pleasure to see Elements take off, and GN evolve into a timely source of important announcements and information about cutting-edge science since I stepped down as co-editor. I feel very fortunate to work with so many outstanding colleagues in the global geochemical community, and I am a little embarrassed, and also very grateful, to have been selected for the Geochemical Society Distinguished Service Award. Thank you!

Paleoclimates and geomorphological evolution of the Carajas region: geochemical and geochronological evidence

International Nuclear Information System (INIS)

Vasconcelos, P.M.

1996-01-01

Based on the geochronological results, on the petrographical and geochemical observations and considering the experimental evidences that suggests a great influence of the organic processes in the Manganese geochemistry it's possible to conclude that the dissolution and reprecipitation events of the Manganese oxides in the Carajas region, Para State, Brazil, represents humid and hot periods in the geological history of the region. The weathering dating furnishes information about the continental evolution in the Mesozoic/Cenozoic, difficult or impossible to determine by another methods

An organic geochemical correlation study of some Drmno depresssion crude oils (southern part of the Pannonian Basin, Yugoslavia

Directory of Open Access Journals (Sweden)

D. VITOROVIC

2001-05-01

Full Text Available The results of an investigation of crude oils originating from the Sirakovo and Bradarac-Maljurevac localities (southern part of the Pannonian Basin are reported in this paper. The aim was to estimate the organic geochemical similarity of the crude oils from the Drmno (Kostolac depression oil fields. The nine selected samples originated from reservoir rocks of various depths. Reliable source and organic geochemical maturation parameters served as the basis for the correlation studies. The similar origin of the investigated Drmno depression crude oils was corroborated, characterized by a significant participation of terrestrial precursor biomass. They were shown to be of relatively low maturity and to have been formed during the earlier stages of the diagenet- ic-catagenetic sequence of processes leading to the formation of crude oils, most probably in source rocks ofTertiary age, corresponding to vitrinite reflectances between Ro = 0.70 % and Ro = 0.80 %. The crude oils from Bradarac-Maljurevac seemed to be somewhat less homogeneous with respect to organic geochemical parameters compared to Sirakovo crude oils.

Uranium exploration data and global geochemical baselines: The need for co-ordinated action

International Nuclear Information System (INIS)

Darnley, A.G.

1997-01-01

Public concern about environmental problems continues. In order to assess the magnitude of potential problems it is necessary to have comprehensive information. The absence of quantitative geochemical data to map the surface composition of the earth is one of the major information gaps in present day environmental science. An IAEA Technical Committee meeting held in November 1993 reviewed the uses of uranium exploration data for environmental purposes. Most attention was focussed on data involving radiation measurements. Uranium exploration programmes conducted since 1970 in many countries collected a considerable amount of geochemical survey data, providing information about the distribution of non-radioactive elements in the natural environment. Canada is one of several countries where such data provided the foundation for national geochemical mapping; other countries could benefit from similar actions. Increasing importance is being attached by governments to the need to enact effective environmental legislation concerning ''safe levels'' of many chemical substances. Such legislation requires geochemical variations in the natural environment. It is becoming necessary to make quantitative comparisons of element abundances across national boundaries, and from continent to continent. In 1995 the IAEA, with other organizations, supported UNESCO to publish a report concerned with the establishment of a Global Geochemical Reference Network. This is designed to provide a framework to connect all types of geochemical survey, to move towards international compatibility of data. The report contains recommendations relating to the standardization of field and laboratory methods; the use of the most sensitive analytical techniques; and standardization of data management. Ground and airborne gamma ray spectrometry, and nuclear laboratory techniques are all discussed. Following the publication of the report, the International Union of Geological Sciences has now established a

Statistical treatment of geochemical data and its application in the geologic mapping and in the definition of the geochemical anomalies in the Alvo 2-Corpo 4 -Provincia Mineral de Carajas

International Nuclear Information System (INIS)

Moura, C.A.V.

1982-01-01

It was given a statistical treatment for the geochemical data about soil in the are named Alvo2 - Corpo4- in the Provincia Mineral de Carajas, Para, Brazil, for application of the geological mapping and definition of geochemical anomalies. (A.B.) [pt

Gamma Spectrometric Determination of U, Th, K and Some Geochemical Applications

International Nuclear Information System (INIS)

Dodona, A.; Tashko, A.

2001-01-01

The application of 'in situ' gamma-spectrometric method (''infinite'' environment), made possible the simultanious determination of U, Th and K. 4 channel gamma-spectrometric analyser with NaI(TI) scintilation counter crystal detector (103 cm 3 φ=50x50mm) was used to determin U, Th(more than 1-2 ppm) and K (more than 1%) in laboratory conditions. The detector was inserted into a lead camera and calibrated for measurement geometry with vessel of ''Marineli'' type of a 17o cm 3 volume. The study of main factors, which influence in the gamma spectrometric measurements, (the technical, physical, geometrical and time parameters) has been carried out. International standards of U, Th, K and internal monitoring standard samples are used for the calibration. External analytical control has been realized by other radiometric and chemical methods. The detection limits ( 1 ppm Th, 2ppm U and 1% K) and the relative errors (17-20% for 1-10 ppm U, Th and 10-15% for more than 10 ppm U, Th and more than 1% K) guarantee a quantitative analysis that may be used successfully in the geochemical studies. Some geochemical applications, based on the content of Th, U and Th/U ratio in rocks samples that we have we have analyzed with this method, are shown in this paper. U, Th and their ratio are used as trace elements to indicate the differences between the acidic magmatic rocks of Albania (Th/U ratio=2-6 and>10). The bimodal character of Th/U scattering in ignimbrides and monzonites (Korabi zone) shows that in addition to the ''normal'' rocks, there are also some ones enriched with Th, So, the differential analysis of Th, U, and K may be used as geochemical exploration criteria for the radioactive and non-radioactive mineralization, such as REE (Rare Earth Elements), phospghorites, bauxites, placers etc. (authors)

Geochemical typification of kimberlite and related rocks of the North Anabar region, Yakutia

Science.gov (United States)

Kargin, A. V.; Golubeva, Yu. Yu.

2017-11-01

The results of geochemical typification of kimberlites and related rocks (alneites and carbonatites) of the North Anabar region are presented with consideration of the geochemical specification of their source and estimation of their potential for diamonds. The content of representative trace elements indicates the predominant contribution of an asthenospheric component (kimberlites and carbonatites) in their source, with a subordinate contribution of vein metasomatic formations containing Cr-diopside and ilmenite. A significant contribution of water-bearing potassium metasomatic parageneses is not recognized. According to the complex of geochemical data, the studied rocks are not industrially diamondiferous.

NEW GEOCHEMICAL DATA OF BASALTS IN THE TSOROIDOG AREA, CENTRAL MONGOLIA

Directory of Open Access Journals (Sweden)

T. Oyunchimeg

2017-01-01

Full Text Available At present, geochemical data are widely used for reconstructing geodynamic settings, especially, volcanic rocks of mafic composition, i.e., basalts, because they are widespread in many orogenic belts and are indicative of different geodynamic environments. In general, we propose the reconstruction of the tectonic settings of basalts according to their relationships with associated ocean plate stratigraphy (OPS sediments, their petrogenesis and their geochemical features.

Application of radio-geochemical exploration to investigation on geo-ecological environment

International Nuclear Information System (INIS)

Ye Qingsen

2000-01-01

Taking investigation on radon hazards and natural radioactivity as examples, the author expounds the prospects of the application of radio-geochemical exploration to the investigation on geo-ecological environment. It is especially emphasized that the methods of radio-geochemical exploration can not be only widely applied in the field of traditional radio-geological prospecting but also play an important role in the investigation on geo-ecological environment

Geochemical evolution of groundwater in the Western Delta region of River Godavari, Andhra Pradesh, India

Science.gov (United States)

Nageswara Rao, P. V.; Appa Rao, S.; Subba Rao, N.

2017-05-01

The present study on geochemical evolution of groundwater is taken up to assess the controlling processes of water chemistry in the Western Delta region of the River Godavari (Andhra Pradesh), which is one of the major rice-producing centers in India. The study region is underlain by coarse sand with black clay (buried channels), black silty clay of recent origin (floodplain) and gray/white fine sand of modern beach sediment of marine source (coastal zone), including brown silty clay with fine sand (paleo-beach ridges). Groundwater is mostly brackish and very hard. It is characterized by Na+ > Mg2+ > Ca2+:HCO3 - > Cl- > SO4 2- > NO3 -, Na+ > Mg2+ > Ca2+:Cl- > HCO3 - > SO4 2-, and Mg2+ > Na+ > Ca2+ > or Cl- > or > SO4 2- facies. The ionic relations (Ca2+ + Mg2+:HCO3 -, Ca2+ + Mg2+:SO4 2- + HCO3 -, Na+ + K+:TC, Na+ + K+:Cl- + SO4 2-, HCO3 -:TC, HCO3 -:Ca2+ + Mg2+, Na+:Cl- and Na+:Ca2+) indicate that the rock weathering, mineral dissolution, evaporation and ion exchange are the processes to control the aquifer chemistry. Anthropogenic and marine sources are also the supplementary factors for brackish water quality. These observations are further supported by Gibbs mechanisms that control the water chemistry. Thus, the study suggests that the initial quality of groundwater of geogenic origin has been subsequently modified by the influences of anthropogenic and marine sources.

Geochemical investigation of UMTRAP designated site at Salt Lake City, Utah

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report is the result of a geochemical investigation of the former uranium mill and tailings site at Salt Lake City, Utah. This is one in a series of site specific geochemical investigations performed on the inactive uranium mill tailings included in the Uranium Mill Tailings Remedial Action Project. The objectives of the investigation are to characterize the geochemistry, to determine the contaminant distribution resulting from the former milling activities and tailings, and to infer chemical pathways and transport mechanisms from the contaminant distribution. The results will be used to model contaminant migration and to develop criteria for long-term containment media such as a cover system which is impermeable to contaminant migration. This report assumes a familiarity with the hydrologic conditions of the site and the geochemical concepts underlying the investigation. The results reported are based on a one-time sampling of waters and solid material from the background, the area adjacent to the site, and the site. The solid samples were water extracted to remove easily soluble salts and acid extracted to remove carbonates and hydroxides. The water extracts and solid samples were anlyzed for the major and trace elements. The report includes the methods of sampling, sample processing, analysis, and data interpretation. Four major conclusions are: (1) sediments in the ditches and creeks adjacent to the site contain tailings, however, the waters were generally not contaminated; (2) tailings are mixed with the soils within a meter below the tailings in some locations, however, water-soluble contaminants decrease to below background levels within 30 cm below the tailings; (3) there has not been significant acid seepage into the soils below the tailings; and (4) salt crusts on the tailings contain trace elements, with the elements that form chloride complexes having the greatest accumulation

Application of subinterval area median contrast filtering method in the recognizing of geochemical anomalies

International Nuclear Information System (INIS)

Zhao Ningbo; Fu Jin; Zhang Chuan; Liu Huan

2012-01-01

Traditional geochemical processing method sometimes maybe loses some weak anomalies related to mineralization, the authors can avoid the influence of geology background and can solve the problem of recognizing weak anomalies in the low-background and high-background area with the subinterval area median contrast filtering method. In an area of Jiangxi Province, several new anomalies are identified by this method and uranium mineralized prospects are found among them. (authors)

A national-scale geochemical and mineralogical survey of soils of the conterminous United States

International Nuclear Information System (INIS)

Smith, David B.; Cannon, William F.; Woodruff, Laurel G.

2011-01-01

Highlights: → Sampling for national-scale soil geochemical and mineralogical survey completed for conterminous USA. → Natural variation for most elements is approximately three orders of magnitude. → Composition of soil parent material is the major controlling factor. → Climate (average annual precipitation) is also an important controlling factor for some elements. → Sample archive (4800 sites) available for future investigations. - Abstract: In 2007, the US Geological Survey initiated a low-density (1 site per 1600 km 2 , c. 4800 sites) geochemical and mineralogical survey of soils of the conterminous USA. The ideal sampling protocol at each site includes a sample from 0-5 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The 3 , HClO 4 and HF. Separate methods are used for As, Hg, Se and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling was completed in 2010 with chemical and mineralogical analysis currently underway. Preliminary results for a swath from the central USA to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.

Soil pH controls the environmental availability of phosphorus: Experimental and mechanistic modelling approaches

International Nuclear Information System (INIS)

Devau, Nicolas; Cadre, Edith Le; Hinsinger, Philippe; Jaillard, Benoit; Gerard, Frederic

2009-01-01

Inorganic P is the least mobile major nutrient in most soils and is frequently the prime limiting factor for plant growth in terrestrial ecosystems. In this study, the extraction of soil inorganic P with CaCl 2 (P-CaCl 2 ) and geochemical modelling were combined in order to unravel the processes controlling the environmentally available P (EAP) of a soil over a range of pH values (pH ∼ 4-10). Mechanistic descriptions of the adsorption of cations and anions by the soil constituents were used (1-pK Triple Plane, ion-exchange and NICA-Donnan models). These models are implemented into the geochemical code Visual MINTEQ. An additive approach was used for their application to the surface horizon of a Cambisol. The geochemical code accurately reproduced the concentration of extracted P at the different soil pH values (R 2 = 0.9, RMSE = 0.03 mg kg -1 ). Model parameters were either directly found in the literature or estimated by fitting published experimental results in single mineral systems. The strong agreement between measurements and modelling results demonstrated that adsorption processes exerted a major control on the EAP of the soil over a large range of pH values. An influence of the precipitation of P-containing mineral is discounted based on thermodynamic calculations. Modelling results indicated that the variations in P-CaCl 2 with soil pH were controlled by the deprotonation/protonation of the surface hydroxyl groups, the distribution of P surface complexes, and the adsorption of Ca and Cl from the electrolyte background. Iron-oxides and gibbsite were found to be the major P-adsorbing soil constituents at acidic and alkaline pHs, whereas P was mainly adsorbed by clay minerals at intermediate pH values. This study demonstrates the efficacy of geochemical modelling to understand soil processes, and the applicability of mechanistic adsorption models to a 'real' soil, with its mineralogical complexity and the additional contribution of soil organic matter.

Soil pH controls the environmental availability of phosphorus: Experimental and mechanistic modelling approaches

Energy Technology Data Exchange (ETDEWEB)

Devau, Nicolas [INRA, UMR 1222 Eco and Sols - Ecologie Fonctionnelle et Biogeochimie des Sols (INRA-IRD-SupAgro), Place Viala, F-34060 Montpellier (France); Cadre, Edith Le [Supagro, UMR 1222 Eco and Sols - Ecologie Fonctionnelle et Biogeochimie des Sols (INRA-IRD-SupAgro), Place Viala, F-34060 Montpellier (France); Hinsinger, Philippe; Jaillard, Benoit [INRA, UMR 1222 Eco and Sols - Ecologie Fonctionnelle et Biogeochimie des Sols (INRA-IRD-SupAgro), Place Viala, F-34060 Montpellier (France); Gerard, Frederic, E-mail: gerard@supagro.inra.fr [INRA, UMR 1222 Eco and Sols - Ecologie Fonctionnelle et Biogeochimie des Sols (INRA-IRD-SupAgro), Place Viala, F-34060 Montpellier (France)

2009-11-15

Inorganic P is the least mobile major nutrient in most soils and is frequently the prime limiting factor for plant growth in terrestrial ecosystems. In this study, the extraction of soil inorganic P with CaCl{sub 2} (P-CaCl{sub 2}) and geochemical modelling were combined in order to unravel the processes controlling the environmentally available P (EAP) of a soil over a range of pH values (pH {approx} 4-10). Mechanistic descriptions of the adsorption of cations and anions by the soil constituents were used (1-pK Triple Plane, ion-exchange and NICA-Donnan models). These models are implemented into the geochemical code Visual MINTEQ. An additive approach was used for their application to the surface horizon of a Cambisol. The geochemical code accurately reproduced the concentration of extracted P at the different soil pH values (R{sup 2} = 0.9, RMSE = 0.03 mg kg{sup -1}). Model parameters were either directly found in the literature or estimated by fitting published experimental results in single mineral systems. The strong agreement between measurements and modelling results demonstrated that adsorption processes exerted a major control on the EAP of the soil over a large range of pH values. An influence of the precipitation of P-containing mineral is discounted based on thermodynamic calculations. Modelling results indicated that the variations in P-CaCl{sub 2} with soil pH were controlled by the deprotonation/protonation of the surface hydroxyl groups, the distribution of P surface complexes, and the adsorption of Ca and Cl from the electrolyte background. Iron-oxides and gibbsite were found to be the major P-adsorbing soil constituents at acidic and alkaline pHs, whereas P was mainly adsorbed by clay minerals at intermediate pH values. This study demonstrates the efficacy of geochemical modelling to understand soil processes, and the applicability of mechanistic adsorption models to a 'real' soil, with its mineralogical complexity and the additional

Geophysical and geochemical techniques for exploration of hydrocarbons and minerals

International Nuclear Information System (INIS)

Sittig, M.

1980-01-01

The detailed descriptive information in this book is based on 389 US patents that deal with geophysical and geochemical techniques useful for the exploration of hydrocarbons and minerals. Where it was necessary to round out the complete technological picture, a few paragraphs from cited government reports have been included. These techniques are used in prospecting for oil, coal, oil shale, tar sand and minerals. The patents are grouped under the following chapters: geochemical prospecting; geobiological prospecting; geophysical exploration; magnetic geophysical prospecting; gravitational geophysical prospecting; electrical geophysical prospecting; nuclear geophysical prospecting; seismic geophysical prospecting; and exploratory well drilling. This book serves a double purpose in that it supplies detailed technical information and can be used as a guide to the US patent literature in this field. By indicating all the information that is significant, and eliminating legal jargon and juristic phraseology, this book presents an advanced, industrially oriented review of modern methods of geophysical and geochemical exploration techniques

The geochemical profile of Mn, Co, Cu and Fe in Kerteh Mangrove Forest, Terengganu

International Nuclear Information System (INIS)

Kamaruzzaman, B.Y.; Antotina, A.; Airiza, Z.; Syalindran, S.; Ong, M.C.

2007-01-01

The geochemical profile of Kerteh mangrove sediments was analyzed for the vertical and horizontal distribution. The 100 cm core sediment sample and 15 surface sediments samples were taken from the field. The geochemical elements of Mn, Co, Cu and Fe of the sediments were analyzed. Geochemical proxy of Mn, Co, Cu and Fe were analyzed by using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). The mean concentrations of Mn, Co, Cu and Fe for the vertical distribution were 210.18 μg/ g, 15.55 μg/ g, 43.65 μg/ g and 1.88 μg/ g respectively. on the other hand, the mean concentrations of the geochemical elements for horizontal distributions were 230.50 μg/ g for Mn, 17.57 μg/ g for Co, 43.381 μg/ g for Cu and 2.93 μg/ g for Fe. Enrichment factor and normalization was used to point out the level of pollution. The EF and the normalization indicated that all the geochemical elements were from the natural sources. (author)

A geochemical atlas of North Carolina, USA

Science.gov (United States)

Reid, J.C.

1993-01-01

A geochemical atlas of North Carolina, U.S.A., was prepared using National Uranium Resource Evaluation (NURE) stream-sediment data. Before termination of the NURE program, sampling of nearly the entire state (48,666 square miles of land area) was completed and geochemical analyses were obtained. The NURE data are applicable to mineral exploration, agriculture, waste disposal siting issues, health, and environmental studies. Applications in state government include resource surveys to assist mineral exploration by identifying geochemical anomalies and areas of mineralization. Agriculture seeks to identify areas with favorable (or unfavorable) conditions for plant growth, disease, and crop productivity. Trace elements such as cobalt, copper, chromium, iron, manganese, zinc, and molybdenum must be present within narrow ranges in soils for optimum growth and productivity. Trace elements as a contributing factor to disease are of concern to health professionals. Industry can use pH and conductivity data for water samples to site facilities which require specific water quality. The North Carolina NURE database consists of stream-sediment samples, groundwater samples, and stream-water analyses. The statewide database consists of 6,744 stream-sediment sites, 5,778 groundwater sample sites, and 295 stream-water sites. Neutron activation analyses were provided for U, Br, Cl, F, Mn, Na, Al, V, Dy in groundwater and stream water, and for U, Th, Hf, Ce, Fe, Mn, Na, Sc, Ti, V, Al, Dy, Eu, La, Sm, Yb, and Lu in stream sediments. Supplemental analyses by other techniques were reported on U (extractable), Ag, As, Ba, Be, Ca, Co, Cr, Cu, K, Li, Mg, Mo, Nb, Ni, P, Pb, Se, Sn, Sr, W, Y, and Zn for 4,619 stream-sediment samples. A small subset of 334 stream samples was analyzed for gold. The goal of the atlas was to make available the statewide NURE data with minimal interpretation to enable prospective users to modify and manipulate the data for their end use. The atlas provides only

Central Colorado Assessment Project (CCAP)-Geochemical data for rock, sediment, soil, and concentrate sample media

Science.gov (United States)

Granitto, Matthew; DeWitt, Ed H.; Klein, Terry L.

2010-01-01

This database was initiated, designed, and populated to collect and integrate geochemical data from central Colorado in order to facilitate geologic mapping, petrologic studies, mineral resource assessment, definition of geochemical baseline values and statistics, environmental impact assessment, and medical geology. The Microsoft Access database serves as a geochemical data warehouse in support of the Central Colorado Assessment Project (CCAP) and contains data tables describing historical and new quantitative and qualitative geochemical analyses determined by 70 analytical laboratory and field methods for 47,478 rock, sediment, soil, and heavy-mineral concentrate samples. Most samples were collected by U.S. Geological Survey (USGS) personnel and analyzed either in the analytical laboratories of the USGS or by contract with commercial analytical laboratories. These data represent analyses of samples collected as part of various USGS programs and projects. In addition, geochemical data from 7,470 sediment and soil samples collected and analyzed under the Atomic Energy Commission National Uranium Resource Evaluation (NURE) Hydrogeochemical and Stream Sediment Reconnaissance (HSSR) program (henceforth called NURE) have been included in this database. In addition to data from 2,377 samples collected and analyzed under CCAP, this dataset includes archived geochemical data originally entered into the in-house Rock Analysis Storage System (RASS) database (used by the USGS from the mid-1960s through the late 1980s) and the in-house PLUTO database (used by the USGS from the mid-1970s through the mid-1990s). All of these data are maintained in the Oracle-based National Geochemical Database (NGDB). Retrievals from the NGDB and from the NURE database were used to generate most of this dataset. In addition, USGS data that have been excluded previously from the NGDB because the data predate earliest USGS geochemical databases, or were once excluded for programmatic reasons

Geochemical investigation of groundwater in the Tono area, Japan. Chemical characteristics and groundwater evolution

International Nuclear Information System (INIS)

Iwatsuki, Teruki; Hama, Katsuhiro; Yoshida, Hidekazu

1997-01-01

Geochemical investigations form an important part of the R and D program at the Tono study site, central Japan. Detailed geological structure and groundwater chemistry have been studied to understand the geochemical environment in the sedimentary and crystalline rocks distributed in this area. The chemical evolution of the groundwater in the sedimentary rocks is characterized with the variation in Na + , Ca 2+ and HCO 3 - concentrations, and ion exchange and dissolution of calcite are dominant reactions in the evolution of groundwater. Geological investigation shows that a fracture system of crystalline rock can be classified into:intact zone, moderately fractured zone and intensely fractured zone, according to the frequency and the width of fractures and fractured zones. The groundwater in the intact and fractured zones of crystalline rock are characterized by Na + -Ca 2+ -HCO 3 - or Na + -HCO 3 - dominated water, and Na + -Ca 2+ -Fe 2+ -HCO 3 - dominated water. The chemical evolution of groundwater is, generally, controlled by water-rock interaction between plagioclase, iron minerals and groundwater. The groundwater at depth of G.L.-186m in the crystalline rock at the Tono area is characterized by the mixture between the oxidized surface water and the reduced groundwater. The investigation based on correlation between geological structures and groundwater chemistry can be applied to understand the geochemical environment in deep crystalline rock, and will support the development of a realistic hydrogeochemical model. (author)

Landscape and bio- geochemical strategy for monitoring transformation and reclamation of the soil mining sites

Science.gov (United States)

Korobova, Elena

2010-05-01

Sites of active or abandoned mining represent areas of considerable technogenic impact and need scientifically ground organization of their monitoring and reclamation. The strategy of monitoring and reclamation depends on the scale and character of the physical, chemical and biological consequences of the disturbances. The geochemical studies for monitoring and rehabilitation of the career-dump complexes should methodically account of formation of the particular new landforms and the changes in circulation of the remobilized elements of the soil cover. However, the general strategy should account of both the initial and transformed landscape geochemical structure of the area with due regard to the natural and new content of chemical elements in the environmental components. For example the tailings and waste rocks present new geochemical fields with specifically different concentration of chemical elements that cause formation of new geochemical barriers and landscapes. The way of colonization of the newly formed landscapes depends upon the new geochemical features of the technogenic environment and the adaptive ability of local and intrusive flora. The newly formed biogeochemical anomalies need organization of permanent monitoring not only within the anomaly itself but also of its impact zones. Spatial landscape geochemical monitoring combined with bio-geochemical criteria of threshold concentrations seems to be a helpful tool for decision making on reclamation and operation of the soil mining sites to provide a long-term ecologically sustainable development of the impact zone as a whole.

Version 4. 00 of the MINTEQ geochemical code

Energy Technology Data Exchange (ETDEWEB)

Eary, L.E.; Jenne, E.A.

1992-09-01

The MINTEQ code is a thermodynamic model that can be used to calculate solution equilibria for geochemical applications. Included in the MINTEQ code are formulations for ionic speciation, ion exchange, adsorption, solubility, redox, gas-phase equilibria, and the dissolution of finite amounts of specified solids. Since the initial development of the MINTEQ geochemical code, a number of undocumented versions of the source code and data files have come into use at the Pacific Northwest Laboratory (PNL). This report documents these changes, describes source code modifications made for the Aquifer Thermal Energy Storage (ATES) program, and provides comprehensive listings of the data files. A version number of 4.00 has been assigned to the MINTEQ source code and the individual data files described in this report.

Version 4.00 of the MINTEQ geochemical code

Energy Technology Data Exchange (ETDEWEB)

Eary, L.E.; Jenne, E.A.

1992-09-01

The MINTEQ code is a thermodynamic model that can be used to calculate solution equilibria for geochemical applications. Included in the MINTEQ code are formulations for ionic speciation, ion exchange, adsorption, solubility, redox, gas-phase equilibria, and the dissolution of finite amounts of specified solids. Since the initial development of the MINTEQ geochemical code, a number of undocumented versions of the source code and data files have come into use at the Pacific Northwest Laboratory (PNL). This report documents these changes, describes source code modifications made for the Aquifer Thermal Energy Storage (ATES) program, and provides comprehensive listings of the data files. A version number of 4.00 has been assigned to the MINTEQ source code and the individual data files described in this report.

Magnetic and Geochemical Properties of Andic Soils from the Massif Central, France

Science.gov (United States)

Grison, H.; Petrovsky, E.; Dlouha, S.; Kapicka, A.

2014-12-01

Ferrimagnetic iron oxides are the key magnetic minerals responsible for enhancement of the magnetic susceptibility in soils. Soils with andic properties contain high amount of Fe-oxides, but only few attempts were made to characterize these soils using magnetic methods. Magnetic susceptibility is in particular suitable for its sensitivity and fast measurement; the presence of Fe-oxides can be easily identified directly in the field. The aim of our study is to describe main magnetic and geochemical properties of soils rich in Fe oxides derived from strongly magnetic volcanic basement. The studied sites are located at the basalt parent rock formed during Pleistocene, Pliocene and Miocene. Investigated soils are exposed to the mountainous climate with the perudic soil moisture regime and cryic temperature soil regime. Seven basalt soil profiles with typical andic properties were analyzed down to parent rock by a set of magnetic and geochemical methods. The magnetic susceptibility was measured in situ and in laboratory using the Bartington MS2D and AGICO MFK1. Its temperature dependence was measured in order to assess phase transformations of magnetic minerals using the KLY4. Magnetic data were completed by the hysteresis, IRM and DCD measurements using ADE EV9 VSM. Geochemical data include soil reaction (pH), organic carbon, cations exchange capacity, and extractable iron and aluminium in the soil extracted by a dithionite-citrate, acid-ammonium oxalate and a pyrophosphate solution. Scanning electron microscopy was done for top/sub-soil and rock samples. Geochemical soil properties reflecting iron oxide stability correlate well with mass-specific magnetic susceptibility. Well pronounced relationship was observed between magnetic grain size, precipitation and soil pH, second group is reflecting concentration of feri-magnetic particles and age of parent rock, and the third group reflects degree of weathering and the thermomagnetic indices expressing changes in magneto

National Geochemical Survey Locations and Results for Iowa

Data.gov (United States)

Iowa State University GIS Support and Research Facility — The United States Geological Survey (USGS), in collaboration with other state and federal agencies, industry, and academia, is conducting a National Geochemical...

Modeled near-field environment porosity modifications due to coupled thermohydrologic and geochemical processes

International Nuclear Information System (INIS)

Glassley, W. E.; Nitao, J. J.

1998-01-01

Heat deposited by waste packages in nuclear waste repositories can modify rock properties by instigating mineral dissolution and precipitation along hydrothermal flow pathways. Modeling this reactive transport requires coupling fluid flow to permeability changes resulting from dissolution and precipitation. Modification of the NUFT thermohydrologic (TH) code package to account for this coupling in a simplified geochemical system has been used to model the time- dependent change in porosity, permeability, matrix and fracture saturation, and temperature in the vicinity of waste-emplacement drifts, using conditions anticipated for the potential Yucca Mountain repository. The results show, within a few hundred years, dramatic porosity reduction approximately 10 m above emplacement drifts. Most of this reduction is attributed to deposition of solute load at the boiling front, although some of it also results from decreasing temperature along the flow path. The actual distribution of the nearly sealed region is sensitive to the time- dependent characteristics of the thermal load imposed on the environment and suggests that the geometry of the sealed region can be engineered by managing the waste-emplacement strategy

Geochemical controls on shale groundwaters: Results of reaction path modeling

International Nuclear Information System (INIS)

Von Damm, K.L.; VandenBrook, A.J.

1989-03-01

The EQ3NR/EQ6 geochemical modeling code was used to simulate the reaction of several shale mineralogies with different groundwater compositions in order to elucidate changes that may occur in both the groundwater compositions, and rock mineralogies and compositions under conditions which may be encountered in a high-level radioactive waste repository. Shales with primarily illitic or smectitic compositions were the focus of this study. The reactions were run at the ambient temperatures of the groundwaters and to temperatures as high as 250/degree/C, the approximate temperature maximum expected in a repository. All modeling assumed that equilibrium was achieved and treated the rock and water assemblage as a closed system. Graphite was used as a proxy mineral for organic matter in the shales. The results show that the presence of even a very small amount of reducing mineral has a large influence on the redox state of the groundwaters, and that either pyrite or graphite provides essentially the same results, with slight differences in dissolved C, Fe and S concentrations. The thermodynamic data base is inadequate at the present time to fully evaluate the speciation of dissolved carbon, due to the paucity of thermodynamic data for organic compounds. In the illitic cases the groundwaters resulting from interaction at elevated temperatures are acid, while the smectitic cases remain alkaline, although the final equilibrium mineral assemblages are quite similar. 10 refs., 8 figs., 15 tabs

Determination of geochemical and natural radioactivity characteristics in Bilecik Marble, Turkey

Science.gov (United States)

Yerel Kandemir, Suheyla; Ozbay, Nurgul

2014-05-01

Natural stones are one of the oldest known building materials. There are more than 400 natural stone in Turkey. Recently, the demand for the natural stone types in markets has been increasing rapidly. For this reason, the geochemical and natural radioactivity characteristics of natural stone are very important. Bilecik province is located at the northwest part of Turkey and it is surrounded by Sakarya, Bursa, Eskisehir and Kutahya city. Bilecik is one of the important marble industry regions of Turkey. Thus, the geochemical and natural radioactivity characteristics of Bilecik marble are very important. In this study, Bilecik marble was collected to determine the geochemistry and natural radioactivity. Then, analyses of geochemical and natural radioactivity in the marble samples are interpreted. ACKNOWLEDGMENT This study is supported by Bilecik Seyh Edebali University scientific project (Project Number =2011-02-BIL.03-04).

Process control in biogas plants

DEFF Research Database (Denmark)

Holm-Nielsen, Jens Bo; Oleskowicz-Popiel, Piotr

2013-01-01

Efficient monitoring and control of anaerobic digestion (AD) processes are necessary in order to enhance biogas plant performance. The aim of monitoring and controlling the biological processes is to stabilise and optimise the production of biogas. The principles of process analytical technology...

The role of atomic absorption spectrometry in geochemical exploration

Science.gov (United States)

Viets, J.G.; O'Leary, R. M.

1992-01-01

In this paper we briefly describe the principles of atomic absorption spectrometry (AAS) and the basic hardware components necessary to make measurements of analyte concentrations. Then we discuss a variety of methods that have been developed for the introduction of analyte atoms into the light path of the spectrophotometer. This section deals with sample digestion, elimination of interferences, and optimum production of ground-state atoms, all critical considerations when choosing an AAS method. Other critical considerations are cost, speed, simplicity, precision, and applicability of the method to the wide range of materials sampled in geochemical exploration. We cannot attempt to review all of the AAS methods developed for geological materials but instead will restrict our discussion to some of those appropriate for geochemical exploration. Our background and familiarity are reflected in the methods we discuss, and we have no doubt overlooked many good methods. Our discussion should therefore be considered a starting point in finding the right method for the problem, rather than the end of the search. Finally, we discuss the future of AAS relative to other instrumental techniques and the promising new directions for AAS in geochemical exploration. ?? 1992.

Geochemical signature of columbite-tantalite and environmental impact of radioactive pegmatite mining in the Parelhas region, Rio Grande do Norte, Northeast Brazil

Energy Technology Data Exchange (ETDEWEB)

Moura, Jorge Costa de; Cruz, Paulo R.; Pereira, Valmir, E-mail: jcmoura@cnen.gov.br, E-mail: pcruz@cnen.gov.br, E-mail: vpereira@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN-RJ), Rio de Janeiro, RJ (Brazil); Ludka, Isabel P.; Mendes, Julio C., E-mail: ludka@geologia.ufrj.br, E-mail: julio@geologia.ufrj.br [Universidade Federal de Rio do Janeiro (CCMN/UFRJ), Rio de Janeiro, RJ (Brazil). Centro de Ciencias Matematicas e da Natureza. Dept. de Geologia

2013-07-01

This article comprises geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area is located in the surroundings of the city of Parelhas, in the geotectonic Province of Borborema. It is well known for its thousands of pegmatitic bodies exploited in primitive mines called garimpos. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of U/Th vs. Nb{sub 2}O{sub 5}/Ta{sub 2}O{sub 5} provides geochemical signatures (analytical fingerprints) for the source location of such ore. The new method was tested with coltan samples of commercial batches from the Brazilian states of Amapa and Rondonia and also generated distinct geochemical signatures. A radiometric survey (CPS) to study the environmental impact of gamma radiation was also carried out in several mines and pegmatites. It included in situ measurements of pegmatite walls, enclosing rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and therefore environmental gamma radiation generally is not enhanced to a dangerous level. (author)

Thermodynamic Data for Geochemical Modeling of Carbonate Reactions Associated with CO2 Sequestration - Literature Review

International Nuclear Information System (INIS)

Krupka, Kenneth M.; Cantrell, Kirk J.; McGrail, B. Peter

2010-01-01

Permanent storage of anthropogenic CO 2 in deep geologic formations is being considered as a means to reduce the concentration of atmospheric CO 2 and thus its contribution to global climate change. To ensure safe and effective geologic sequestration, numerous studies have been completed of the extent to which the CO 2 migrates within geologic formations and what physical and geochemical changes occur in these formations when CO 2 is injected. Sophisticated, computerized reservoir simulations are used as part of field site and laboratory CO 2 sequestration studies. These simulations use coupled multiphase flow-reactive chemical transport models and/or standalone (i.e., no coupled fluid transport) geochemical models to calculate gas solubility, aqueous complexation, reduction/oxidation (redox), and/or mineral solubility reactions related to CO 2 injection and sequestration. Thermodynamic data are critical inputs to modeling geochemical processes. The adequacy of thermodynamic data for carbonate compounds has been identified as an important data requirement for the successful application of these geochemical reaction models to CO 2 sequestration. A review of thermodynamic data for CO 2 gas and carbonate aqueous species and minerals present in published data compilations and databases used in geochemical reaction models was therefore completed. Published studies that describe mineralogical analyses from CO 2 sequestration field and natural analogue sites and laboratory studies were also reviewed to identify specific carbonate minerals that are important to CO 2 sequestration reactions and therefore require thermodynamic data. The results of the literature review indicated that an extensive thermodynamic database exists for CO 2 and CH 4 gases, carbonate aqueous species, and carbonate minerals. Values of Δ f G 298 o and/or log K r,298 o are available for essentially all of these compounds. However, log K r,T o or heat capacity values at temperatures above 298 K exist

Probabilistic, sediment-geochemical parameterisation of the groundwater compartment of the Netherlands for spatially distributed, reactive transport modelling

Science.gov (United States)

Janssen, Gijs; Gunnink, Jan; van Vliet, Marielle; Goldberg, Tanya; Griffioen, Jasper

2017-04-01

Pollution of groundwater aquifers with contaminants as nitrate is a common problem. Reactive transport models are useful to predict the fate of such contaminants and to characterise the efficiency of mitigating or preventive measures. Parameterisation of a groundwater transport model on reaction capacity is a necessary step during building the model. Two Dutch, national programs are combined to establish a methodology for building a probabilistic model on reaction capacity of the groundwater compartment at the national scale: the Geological Survey program and the NHI Netherlands Hydrological Instrument program. Reaction capacity is considered as a series of geochemical characteristics that control acid/base condition, redox condition and sorption capacity. Five primary reaction capacity variables are characterised: 1. pyrite, 2. non-pyrite, reactive iron (oxides, siderite and glauconite), 3. clay fraction, 4. organic matter and 5. Ca-carbonate. Important reaction capacity variables that are determined by more than one solid compound are also deduced: 1. potential reduction capacity (PRC) by pyrite and organic matter, 2. cation-exchange capacity (CEC) by organic matter and clay content, 3. carbonate buffering upon pyrite oxidation (CPBO) by carbonate and pyrite. Statistical properties of these variables are established based on c. 16,000 sediment geochemical analyses. The first tens of meters are characterised based on 25 regions using combinations of lithological class and geological formation as strata. Because of both less data and more geochemical uniformity, the deeper subsurface is characterised in a similar way based on 3 regions. The statistical data is used as input in an algoritm that probabilistically calculates the reaction capacity per grid cell. First, the cumulative frequency distribution (cfd) functions are calculated from the statistical data for the geochemical strata. Second, all voxel cells are classified into the geochemical strata. Third, the

Geochemical prospect ion results of Mariscala aerial photo

International Nuclear Information System (INIS)

Filippini, J.

1989-01-01

This report shows the geochemical prospect ion results carried out within the framework of the metalical mining prospect ion in Mariscala aerial photo. Lavalleja district belong to the Mining inventory programme of Uruguay.

Geochemical methodology for gold prospect ion in Uruguay

International Nuclear Information System (INIS)

Spangenber, J.

1987-01-01

This work is about the history of gold prospection in Uruguay. In this study there are considered the geochemical aspects, the gold performance, the applicability to mining prospection and the gold prospection aluvionar

Geochemical Triggers of Arsenic Mobilization during Managed Aquifer Recharge.

Science.gov (United States)

Fakhreddine, Sarah; Dittmar, Jessica; Phipps, Don; Dadakis, Jason; Fendorf, Scott

2015-07-07

Mobilization of arsenic and other trace metal contaminants during managed aquifer recharge (MAR) poses a challenge to maintaining local groundwater quality and to ensuring the viability of aquifer storage and recovery techniques. Arsenic release from sediments into solution has occurred during purified recycled water recharge of shallow aquifers within Orange County, CA. Accordingly, we examine the geochemical processes controlling As desorption and mobilization from shallow, aerated sediments underlying MAR infiltration basins. Further, we conducted a series of batch and column experiments to evaluate recharge water chemistries that minimize the propensity of As desorption from the aquifer sediments. Within the shallow Orange County Groundwater Basin sediments, the divalent cations Ca(2+) and Mg(2+) are critical for limiting arsenic desorption; they promote As (as arsenate) adsorption to the phyllosilicate clay minerals of the aquifer. While native groundwater contains adequate concentrations of dissolved Ca(2+) and Mg(2+), these cations are not present at sufficient concentrations during recharge of highly purified recycled water. Subsequently, the absence of dissolved Ca(2+) and Mg(2+) displaces As from the sediments into solution. Increasing the dosages of common water treatment amendments including quicklime (Ca(OH)2) and dolomitic lime (CaO·MgO) provides recharge water with higher concentrations of Ca(2+) and Mg(2+) ions and subsequently decreases the release of As during infiltration.

Potential accumulation of contaminated sediments in a reservoir of a high-Andean watershed: Morphodynamic connections with geochemical processes

Science.gov (United States)

Contreras, María. Teresa; Müllendorff, Daniel; Pastén, Pablo; Pizarro, Gonzalo E.; Paola, Chris; Escauriaza, Cristián.

2015-05-01

Rapid changes due to anthropic interventions in high-altitude environments, such as the Altiplano region in South America, require new approaches to understand the connections between physical and geochemical processes. Alterations of the water quality linked to the river morphology can affect the ecosystems and human development in the long term. The future construction of a reservoir in the Lluta River, located in northern Chile, will change the spatial distribution of arsenic-rich sediments, which can have significant effects on the lower parts of the watershed. In this investigation, we develop a coupled numerical model to predict and evaluate the interactions between morphodynamic changes in the Lluta reservoir, and conditions that can potentially desorb arsenic from the sediments. Assuming that contaminants are mobilized under anaerobic conditions, we calculate the oxygen concentration within the sediments to study the interactions of the delta progradation with the potential arsenic release. This work provides a framework for future studies aimed to analyze the complex connections between morphodynamics and water quality, when contaminant-rich sediments accumulate in a reservoir. The tool can also help to design effective risk management and remediation strategies in these extreme environments. This article was corrected on 15 JUNE 2015. See the end of the full text for details.

Role of Dissolved Organic Matter and Geochemical Controls on Arsenic Cycling from Sediments to Groundwater along the Meghna River, Bangladesh: Tracking possible links to permeable natural reactive barrier

Science.gov (United States)

Datta, S.; Berube, M.; Knappett, P.; Kulkarni, H. V.; Vega, M.; Jewell, K.; Myers, K.

2017-12-01

Elevated levels of dissolved arsenic (As), iron (Fe) and manganese (Mn) are seen in the shallow groundwaters of southeast Bangladesh on the Ganges Brahmaputra Meghna River delta. This study takes a multi disciplinary approach to understand the extent of the natural reactive barrier (NRB) along the Meghna River and evaluate the role of the NRB in As sequestration and release in groundwater aquifers. Shallow sediment cores, and groundwater and river water samples were collected from the east and west banks of the Meghna. Groundwater and river water samples were tested for FeT, MnT, and AsT concentrations. Fluorescence spectroscopic characterization of groundwater dissolved organic matter (DOM) provided insight into the hydro geochemical reactions active in the groundwater and the hyporheic zones. Eight sediment cores of 1.5 m depth were collected 10 m away from the edge of the river. Vertical solid phase concentration profiles of Fe, Mn and As were measured via 1.2 M HCl digestion which revealed solid phase As accumulation along the riverbanks up to concentrations of 1500 mg/kg As. Microbial interactions with DOM prompts the reduction of Fe3+ to Fe2+, causing As to mobilize into groundwater and humic-like DOM present in the groundwater may catalyze this process. The extent to which microbially mediated release of As occurs is limited by labile dissolved organic carbon (DOC) availability. Aqueous geochemical results showed the highest dissolved As concentrations in shallow wells (groundwater was found to contain microbial and terrestrial derived DOC, and decomposed, humified and aromatic DOM. Deeper aquifers had a significantly larger microbial OM signature than the shallower aquifers and was less aromatic, decomposed and humified. The results from this study illustrate the potential for humic substances to contribute to As cycling and quantify the extent of As accumulation in the sediments and groundwater along a 1 km stretch of the Meghna. These findings contribute

Temporal variability of secondary processes in alkaline geothermal waters associated to granitic rocks: the Caldes de Boí geothermal system (Spain)

International Nuclear Information System (INIS)

Asta, M.; Gimeno, M.J.; Auqué, L.F.; Galve, J.P.; Gómez, J.; Acero, P.; Lapuente, P.

2017-01-01

The Caldes de Boí geothermal waters show important differences in pH (6.5–9.6) and temperature (15.9ºC–52ºC) despite they have a common origin and a very simple circuit at depth (4km below the recharge area level). Thes differences are the result of secondary processes such as conductive cooling, mixing with colder shallower waters, and input of external CO2, which affect each spring to a different extent in the terminal part of the thermal circuit. In this paper, the secondary processes that control the geochemical evolution of this system have been addressed using a geochemical dataset spanning over 20 years and combining different approaches: classical geochemical calculations and geochemical modelling. Mixing between a cold and a thermal end-member, cooling and CO2 exchange are the processes affecting the spring waters with different intensity over time. These differences in the intensity of the secondary processes could be controlled by the effect of climate and indirectly by the geomorphological and hydrogeological setting of the different springs. Infiltration recharging the shallow aquifer is dominant during the rainy seasons and the extent of the mixing process is greater, at least in some springs.Moreover, significant rainfall can produce a decrease in the ground temperature favouring the conductive cooling. Finally, the geomorphological settings of the springs determine the thickness and the hydraulic properties of the saturated layer below them and, therefore, they affect the extent of the mixing process between the deep thermal waters and the shallower cold waters. The understanding of the compositional changes in the thermal waters and the main factors that could affect them is a key issue to plan the future management of the geothermal resources of the Caldes de Boí system. Here, we propose to use a simple methodology to assess the effect of those factors, which could affect the quality of the thermal waters for balneotherapy at long

Temporal variability of secondary processes in alkaline geothermal waters associated to granitic rocks: the Caldes de Boí geothermal system (Spain)

Energy Technology Data Exchange (ETDEWEB)

Asta, M.; Gimeno, M.J.; Auqué, L.F.; Galve, J.P.; Gómez, J.; Acero, P.; Lapuente, P.

2017-11-01

The Caldes de Boí geothermal waters show important differences in pH (6.5–9.6) and temperature (15.9ºC–52ºC) despite they have a common origin and a very simple circuit at depth (4km below the recharge area level). Thes differences are the result of secondary processes such as conductive cooling, mixing with colder shallower waters, and input of external CO2, which affect each spring to a different extent in the terminal part of the thermal circuit. In this paper, the secondary processes that control the geochemical evolution of this system have been addressed using a geochemical dataset spanning over 20 years and combining different approaches: classical geochemical calculations and geochemical modelling. Mixing between a cold and a thermal end-member, cooling and CO2 exchange are the processes affecting the spring waters with different intensity over time. These differences in the intensity of the secondary processes could be controlled by the effect of climate and indirectly by the geomorphological and hydrogeological setting of the different springs. Infiltration recharging the shallow aquifer is dominant during the rainy seasons and the extent of the mixing process is greater, at least in some springs.Moreover, significant rainfall can produce a decrease in the ground temperature favouring the conductive cooling. Finally, the geomorphological settings of the springs determine the thickness and the hydraulic properties of the saturated layer below them and, therefore, they affect the extent of the mixing process between the deep thermal waters and the shallower cold waters. The understanding of the compositional changes in the thermal waters and the main factors that could affect them is a key issue to plan the future management of the geothermal resources of the Caldes de Boí system. Here, we propose to use a simple methodology to assess the effect of those factors, which could affect the quality of the thermal waters for balneotherapy at long

Geochemical modelling of groundwater evolution and residence time at the Olkiluoto site

International Nuclear Information System (INIS)

Pitkaenen, P.; Luukkonen, A.; Ruotsalainen, P.; Leino-Forsman, H.; Vuorinen, U.

1999-05-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the crystalline bedrock at Olkiluoto has been created and the significance of chemical reactions and groundwater mixing along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on water samples (63 altogether) obtained from precipitation, Baltic Sea, soil layer, shallow wells in the bedrock, and eight deep boreholes in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and fracture calcite and their isotopic measurements were also utilised. The data covers the bedrock at Olkiluoto to a depth of 1000 m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and mixing of palaeo water types were approached by mass-balance calculations (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The interpretation and calculation of hydrochemical data from Olkiluoto reveals the complex nature of hydrogeochemical evolution at the site. Changes in

Geochemical modelling of groundwater evolution and residence time at the Olkiluoto site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy (Finland); Leino-Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

1999-05-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the crystalline bedrock at Olkiluoto has been created and the significance of chemical reactions and groundwater mixing along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on water samples (63 altogether) obtained from precipitation, Baltic Sea, soil layer, shallow wells in the bedrock, and eight deep boreholes in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and fracture calcite and their isotopic measurements were also utilised. The data covers the bedrock at Olkiluoto to a depth of 1000 m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and mixing of palaeo water types were approached by mass-balance calculations (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The interpretation and calculation of hydrochemical data from Olkiluoto reveals the complex nature of hydrogeochemical evolution at the site. Changes in

Geochemical landscapes of the conterminous United States; new map presentations for 22 elements

Science.gov (United States)

Gustavsson, N.; Bolviken, B.; Smith, D.B.; Severson, R.C.

2001-01-01

Geochemical maps of the conterminous United States have been prepared for seven major elements (Al, Ca, Fe, K, Mg, Na, and Ti) and 15 trace elements (As, Ba, Cr, Cu, Hg, Li, Mn, Ni, Pb, Se, Sr, V, Y, Zn, and Zr). The maps are based on an ultra low-density geochemical survey consisting of 1,323 samples of soils and other surficial materials collected from approximately 1960-1975. The data were published by Boerngen and Shacklette (1981) and black-and-white point-symbol geochemical maps were published by Shacklette and Boerngen (1984). The data have been reprocessed using weighted-median and Bootstrap procedures for interpolation and smoothing.

Microcrystalline silicon deposition: Process stability and process control

International Nuclear Information System (INIS)

Donker, M.N. van den; Kilper, T.; Grunsky, D.; Rech, B.; Houben, L.; Kessels, W.M.M.; Sanden, M.C.M. van de

2007-01-01

Applying in situ process diagnostics, we identified several process drifts occurring in the parallel plate plasma deposition of microcrystalline silicon (μc-Si:H). These process drifts are powder formation (visible from diminishing dc-bias and changing spatial emission profile on a time scale of 10 0 s), transient SiH 4 depletion (visible from a decreasing SiH emission intensity on a time scale of 10 2 s), plasma heating (visible from an increasing substrate temperature on a time scale of 10 3 s) and a still puzzling long-term drift (visible from a decreasing SiH emission intensity on a time scale of 10 4 s). The effect of these drifts on the crystalline volume fraction in the deposited films is investigated by selected area electron diffraction and depth-profiled Raman spectroscopy. An example shows how the transient depletion and long-term drift can be prevented by suitable process control. Solar cells deposited using this process control show enhanced performance. Options for process control of plasma heating and powder formation are discussed

The geochemical behavior of protactinium 231 and its chosen geochemical analogue thorium in the biosphere

International Nuclear Information System (INIS)

Gillberg-Wickman, M.

1983-03-01

To be able to judge whether protactinium 231 might represent a major contribution to the human radiation risk from high level radioactive waste a literature study of the geochemical behavior of protactinium has been made. The interest in protactinium determinations has, as far, been in the field of marine geochemistry and geochronology. These investigations show that thorium may be used as a chemical analogue. The content of protactinium 231 is determined by the 235 U content and consequently the occurrence of protactinium in nature is directly associated to the geochemistry of uranium. The pronounced hydrolytic tendency of protactinium and its great sorption and coprecipitation capacity ought to prevent or at least appreciably delay its transport from a back-filled nuclear waste vault to the uppermost surface of the earth. It also has a tendency to form colloids or particulates which may be strongly fixed on a rock surface. In adsorption and desorption processes kinetics must play an important role. Our knowledge in this field is quite limited. Under the physico-chemical conditions in the sea, protactinium is rapidly scavenged from the water column by particulates. It accumulates in the sediments. (author)

Geochemical mapping in polluted floodplains using handheld XRF, geophysical imaging, and geostatistics

Science.gov (United States)

Hošek, Michal; Matys Grygar, Tomáš; Popelka, Jan; Kiss, Timea; Elznicová, Jitka; Faměra, Martin

2017-04-01

units. Those findings must, however, be checked by sediment examination and analysis in selected points. We processed the crucial characteristics obtained by geochemical mapping, namely depth of maximum pollution, amount of contamination, and lithology (Al/Si and Zr/Rb ratios), using geostatistics. Moreover, some parts of floodplain were dated by optically stimulated luminescence (OSL) which revealed, that recycling of top decimetres of floodplain fine fill (silts) in Boreček site has proceeded relatively recently (in decades and centuries) as compared to deeper lying coarser (sandy) strata (millennia). The results of geochemical mapping show complexity of pollution hotspots and need of their integrated interpretation. Key words: Dipole electromagneting profilling, electric resistivity tomography, floodplain contamination, geochemical mapping

An integrated approach to process control

NARCIS (Netherlands)

Schippers, W.A.J.

2001-01-01

The control of production processes is the subject of several disciplines, such as statistical process control (SPC), total productive maintenance (TPM), and automated process control (APC). Although these disciplines are traditionally separated (both in science and in business practice), their

Environmental and geochemical assessment of surface sediments on irshansk ilmenite deposit area

Directory of Open Access Journals (Sweden)

Наталия Олеговна Крюченко

2015-03-01

Full Text Available It is revealed the problem of pollution of surface sediments of Irshansk ilmenite deposit area of various chemical elements hazard class (Mn, V, Ba, Ni, Co, Cr, Mo, Cu, Pb, Zn. It is determined its average content in surface sediments of various functional areas (forest and agricultural land, flood deposits, reclaimed land, calculated geochemical criteria, so given ecological and geochemical assessment of area

Geochemical modeling of magmatic gas scrubbing

Directory of Open Access Journals (Sweden)

B. Gambardella

2005-06-01

Full Text Available The EQ3/6 software package, version 7.2 was successfully used to model scrubbing of magmatic gas by pure water at 0.1 MPa, in the liquid and liquid-plus-gas regions. Some post-calculations were necessary to account for gas separation effects. In these post-calculations, redox potential was considered to be fixed by precipitation of crystalline a-sulfur, a ubiquitous and precocious process. As geochemical modeling is constrained by conservation of enthalpy upon water-gas mixing, the enthalpies of the gas species of interest were reviewed, adopting as reference state the liquid phase at the triple point. Our results confirm that significant emissions of highly acidic gas species (SO2(g, HCl(g, and HF(g are prevented by scrubbing, until dry conditions are established, at least locally. Nevertheless important outgassing of HCl(g can take place from acid, HCl-rich brines. Moreover, these findings support the rule of thumb which is generally used to distinguish SO2-, HCl-, and HF-bearing magmatic gases from SO2-, HCl-, and HF-free hydrothermal gases.

Statistical process control in wine industry using control cards

OpenAIRE

Dimitrieva, Evica; Atanasova-Pacemska, Tatjana; Pacemska, Sanja

2013-01-01

This paper is based on the research of the technological process of automatic filling of bottles of wine in winery in Stip, Republic of Macedonia. The statistical process control using statistical control card is created. The results and recommendations for improving the process are discussed.

Geochemical modeling of the nuclear-waste repository system. A status report

International Nuclear Information System (INIS)

Deutsch, W.J.

1980-12-01

The primary objective of the geochemical modeling task is to develop an understanding of the waste-repository geochemical system and provide a valuable tool for estimating future states of that system. There currently exists a variety of computer codes which can be used in geochemical modeling studies. Some available codes contain the framework for simulating a natural chemical system and estimating, within limits, the response of that system to environmental changes. By data-base enhancement and code development, this modeling technique can be even more usefully applied to a nuclear-waste repository. In particular, thermodynamic data on elements not presently in the data base but identified as being of particular hazard in the waste-repository system, need to be incorporated into the code to estimate the near-field as well as the far-field reactions during a hypothetical breach. A reaction-path-simulation code, which estimates the products of specific rock/water reactions, has been tested using basalt and ground water. Results show that the mass-transfer capabilities of the code will be useful in chemical-evolution studies and scenario analyses. The purpose of this report is to explain the status of geochemical modeling as it currently applies to the chemical system of a hypothetical nuclear-waste repository in basalt and to present the plan proposed for further developmet and application

X-Ray and Radiometrics in Geo-Ecological and Geochemical Mapping

Energy Technology Data Exchange (ETDEWEB)

Fedyanin, S. N. [Navoi Mining and Metallurgical Combinat (Uzbekistan)

2014-05-15

Monitoring of tailing pits of uranium ore conversion products and reserve supplies of low-grade ores stored in dumps is traditionally based on radiation environment on these sites and adjacent territories. The results of gamma-ray spectrometry of solid fractions and radon concentration measurement in liquid and gas phases of technogenic formations are used in radiation hazard evaluation. Radiometric testing practice of low-activity field formations in loose and lump masses shows that due to high emanating ability it is necessary to use dual-channel radiometer for ionizing radiation background record and compensation. Thus gamma-radiometry is not the direct method of uranium content determination and alfa- and beta-radiometry can be correctly used only for sample analysis in laboratory environment. Consequently, distant express testing with the help of X-ray radiometric (XRM) instruments (on calcium, iron, manganese, titanium, copper, arsenic, lead, strontium, selenium, molybdenum, uranium, etc.) is recommended for additional introduction in field observations of radio-ecological environment in mining and processing production tailing and dumps of low-grade ore reserve supplies. Thanks to preliminary areal schemes of geochemical zonality as per XRM data XRM application allows to use the sample limit, given for a wide range of laboratory analyses rationally. Sampling places and their number as well as kinds of laboratory analyses are chosen based on XRM data.It is rather effective to use laboratory variant of atomic absorptive analysis on mercury and stibium in gases (GA), generated in the process of grated samples calcination in muffle furnaces. During the presentation of the report In order to prove the effectiveness of XRM and GA presentation graphics with the results of areal mapping using the above methods and geochemical testing on the territories of Tashkent (Uzbekistan) and Chimkent (Kazakhstan) regions within the framework of the geological and ecological

Geothermal investigations with isotope and geochemical techniques in Latin America

International Nuclear Information System (INIS)

1992-03-01

The IAEA Co-ordinated Research Programme (CRP) for Latin America on the Use of Isotope and Geochemical Techniques in Geothermal Exploration started in 1984. The first activity carried out was a Seminar on isotope and geochemical techniques in geothermal exploration, which took place in June 1984 in Morelia, Mexico. During the seminar, which was attended by representatives of the institutions which later took part in the programme, the objectives, main research lines, and geothermal fields to be studied during the CRP were discussed. The first research contracts were awarded towards the end of 1984. The field work started in 1985 and continued through 1990. During the implementation of the CRP a considerable number of geothermal fields were studied in the nine participating countries. The investigations carried out were geochemically quite comprehensive in most cases, but in some others they were still in a reconnaissance stage when the CRP ended: the latter studies are not reported in these proceedings, but the data obtained are in principle available from the relevant national institutions. While investigations with conventional geochemical techniques had already started in several fields before 1985, isotope methods were applied for the first time in all cases during this CRP. Due to the remoteness and high elevation of many of the fields studied and the adverse meteorological conditions during long periods of the year, the investigations could not proceed rapidly: this is the main reason for the unusually long duration of the CRP, which could be concluded only after more than five years after its inception

Use of natural geochemical tracers to improve reservoir simulation models

Energy Technology Data Exchange (ETDEWEB)

Huseby, O.; Chatzichristos, C.; Sagen, J.; Muller, J.; Kleven, R.; Bennett, B.; Larter, S.; Stubos, A.K.; Adler, P.M.

2005-01-01

This article introduces a methodology for integrating geochemical data in reservoir simulations to improve hydrocarbon reservoir models. The method exploits routine measurements of naturally existing inorganic ion concentration in hydrocarbon reservoir production wells, and uses the ions as non-partitioning water tracers. The methodology is demonstrated on a North Sea field case, using the field's reservoir model, together with geochemical information (SO{sub 4}{sup 2}, Mg{sup 2+} K{sup +}, Ba{sup 2+}, Sr{sup 2+}, Ca{sup 2+}, Cl{sup -} concentrations) from the field's producers. From the data-set we show that some of the ions behave almost as ideal sea-water tracers, i.e. without sorption to the matrix, ion-exchange with the matrix or scale-formation with other ions in the formation water. Moreover, the dataset shows that ion concentrations in pure formation-water vary according to formation. This information can be used to allocate produced water to specific water-producing zones in commingled production. Based on an evaluation of the applicability of the available data, one inorganic component, SO{sub 4}{sup 2}, is used as a natural seawater tracer. Introducing SO{sub 4}{sup 2} as a natural tracer in a tracer simulation has revealed a potential for improvements of the reservoir model. By tracking the injected seawater it was possible to identify underestimated fault lengths in the reservoir model. The demonstration confirms that geochemical data are valuable additional information for reservoir characterization, and shows that integration of geochemical data into reservoir simulation procedures can improve reservoir simulation models. (author)

Memory-type control charts in statistical process control

NARCIS (Netherlands)

Abbas, N.

2012-01-01

Control chart is the most important statistical tool to manage the business processes. It is a graph of measurements on a quality characteristic of the process on the vertical axis plotted against time on the horizontal axis. The graph is completed with control limits that cause variation mark. Once

Geochemical modelling of the weathering zone of the 'Mina Fe' U deposit (Spain): A natural analogue for nuclear spent fuel alteration and stability processes in radwaste disposal

International Nuclear Information System (INIS)

Arcos, D.; Perez del Villar, L.; Bruno, J.; Domenech, C.

2008-01-01

The 'Mina Fe' U deposit (Salamanca, Spain) has been studied in the context of Enresa's programme for U-mine sites restoration and also as a natural analogue for processes in high-level nuclear waste (HLNW) geological disposal. The investigations encompassed an array of geoscience disciplines, such as structural geology, mineralogy, hydrogeology and elemental and isotopic geochemistry and hydrogeochemistry of the site. Based on the obtained results, a conceptual mineralogical and geochemical model was performed integrating the main geochemical processes occurring at the site: the interaction between oxidised and slightly acidic water with pyrite, pitchblende, calcite and dolomite, as essential minerals of the U fracture-filling mineralisation, and hydroxyapatite from the host rock, as the main source of P. This conceptual model has been tested in a systematic numerical model, which includes the main kinetic (pyrite and pitchblende dissolution) and equilibrium processes (carbonate mineral dissolution, and goethite, schoepite and autunite secondary precipitation). The results obtained from the reactive-transport model satisfactorily agree with the conceptual model previously established. The assumption of the precipitation of coffinite as a secondary mineral in the system cannot be correctly evaluated due to the lack of hydrochemical data from the reducing zone of the site and valid thermodynamic and kinetic data for this hydrated U(IV)-silicate. This precipitation can also be hampered by the probable existence of dissolved U(IV)-organic matter and/or uranyl carbonate complexes, which are thermodynamically stable under the alkaline and reducing conditions that prevail in the reducing zone of the system. Finally, the intense downwards oxic and acidic alteration in the upper part of the system is of no relevance for the performance assessment of a HLNW disposal. However, the acidic and oxidised conditions are quickly buffered to neutral-alkaline and reducing at very

Geochemical characterisation of Elbe river high flood sediments

Energy Technology Data Exchange (ETDEWEB)

Krueger, F. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Falkenberg (Germany). Sektion Boden-/Gewaesserforschung]|[UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Magdeburg (Germany). Sektion Gewaesserforschung; Rupp, H.; Meissner, R. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Falkenberg (Germany). Sektion Boden-/Gewaesserforschung; Lohse, M.; Buettner, O.; Friese, K. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Magdeburg (Germany). Sektion Gewaesserforschung; Miehlich, G. [Hamburg Univ. (Germany). Inst. fuer Bodenkunde

2001-07-01

Quality aims for land usage in flood plains have to be worked out in the Russian-German research project 'Effects of floods on the pollution of agricultural used flood plain soils of the Oka River and the Elbe River'. It is financed by the Germany Ministry of Education and Research (FKZ 02 WT 9617/0). Beside the characterisation of the present pollution of soils for the middle Elbe, it is necessary to prognosticate the current pollutant input. At the examination site nearby Wittenberge, Elbe River kilometers 435 and 440, natural deposited flood sediments were sampled by artificial lawn mats. By the geochemical characterisation it is possible to record the metal input into the flood plain and to win knowledge about the sedimentation process. The results of sediment investigation of the high flood in spring 1997 are presented. (orig.)

Geochemical modelling of the sorption of tetravalent radioelements

International Nuclear Information System (INIS)

Bond, K.A.; Tweed, C.J.

1991-05-01

The results of an experimental study of the sorption of a range of tetravalent radioelements, plutonium (IV), tin (IV), thorium(IV) and uranium(IV), onto clay at pH8 and pH11 have been successfully simulated using a triple layer sorption model. The model has been incorporated into HARPHRQ, a geochemical program based on PHREEQE. The model has been parameterised using data for sorption onto ferric oxyhydroxide and goethite. The effects of hydroxycarboxylic acids on the sorption process have also been investigated experimentally. It was generally observed that in the presence of 2x10 -3 M gluconate, sorption was reduced by up two orders of magnitude. The model has satisfactorily simulated these lower sorptivities, through assuming competing sorption and complexation reactions. This work, therefore, further confirms the need to take account of such organic materials in safety assessment modelling. (author)

Estimation of Supraglacial Dust and Debris Geochemical Composition via Satellite Reflectance and Emissivity

Science.gov (United States)

Casey, Kimberly Ann; Kaab, Andreas

2012-01-01

We demonstrate spectral estimation of supraglacial dust, debris, ash and tephra geochemical composition from glaciers and ice fields in Iceland, Nepal, New Zealand and Switzerland. Surface glacier material was collected and analyzed via X-ray fluorescence spectroscopy (XRF) and X-ray diffraction (XRD) for geochemical composition and mineralogy. In situ data was used as ground truth for comparison with satellite derived geochemical results. Supraglacial debris spectral response patterns and emissivity-derived silica weight percent are presented. Qualitative spectral response patterns agreed well with XRF elemental abundances. Quantitative emissivity estimates of supraglacial SiO2 in continental areas were 67% (Switzerland) and 68% (Nepal), while volcanic supraglacial SiO2 averages were 58% (Iceland) and 56% (New Zealand), yielding general agreement. Ablation season supraglacial temperature variation due to differing dust and debris type and coverage was also investigated, with surface debris temperatures ranging from 5.9 to 26.6 C in the study regions. Applications of the supraglacial geochemical reflective and emissive characterization methods include glacier areal extent mapping, debris source identification, glacier kinematics and glacier energy balance considerations.

Estimation of Supraglacial Dust and Debris Geochemical Composition via Satellite Reflectance and Emissivity

Directory of Open Access Journals (Sweden)

Kimberly Casey

2012-09-01

Full Text Available We demonstrate spectral estimation of supraglacial dust, debris, ash and tephra geochemical composition from glaciers and ice fields in Iceland, Nepal, New Zealand and Switzerland. Surface glacier material was collected and analyzed via X-ray fluorescence spectroscopy (XRF and X-ray diffraction (XRD for geochemical composition and mineralogy. In situ data was used as ground truth for comparison with satellite derived geochemical results. Supraglacial debris spectral response patterns and emissivity-derived silica weight percent are presented. Qualitative spectral response patterns agreed well with XRF elemental abundances. Quantitative emissivity estimates of supraglacial SiO2 in continental areas were 67% (Switzerland and 68% (Nepal, while volcanic supraglacial SiO2 averages were 58% (Iceland and 56% (New Zealand, yielding general agreement. Ablation season supraglacial temperature variation due to differing dust and debris type and coverage was also investigated, with surface debris temperatures ranging from 5.9 to 26.6 C in the study regions. Applications of the supraglacial geochemical reflective and emissive characterization methods include glacier areal extent mapping, debris source identification, glacier kinematics and glacier energy balance considerations.

Kinetic and thermodynamic modelling of geochemical effects of a nuclear waste storage in granitic environment

International Nuclear Information System (INIS)

Made, B.; Fritz, B.

1993-01-01

In the world, various experimental sites are selected to study the behavior of different types of source rocks under nuclear waste storage influence. The surrounding rock tested to receive the waste storage must be a stable geological formation. In France, four geological formations are preselected for the feasibility study of repository for spent nuclear fuel at long term: shale, salt, clay and granite. At present time, numerous studies are carried out in Europe (Germany, Belgium, Sweden, Switzerland, United-Kingdom...), in North America (U.S.A. and Canada) and in Japan. Water-rock interactions control the most of rock transformations near the surface of the earth. The rock forming minerals react with the aqueous solutions, the primary minerals dissolution releases ionic species in solution and secondary minerals precipitate if equilibrium or oversaturation is reached. The weathering processes (hydrothermal or not) are always very complicated thus, geochemical codes has been developed to simulate the water-rock interactions. The first generation of codes is based on purely thermodynamic laws without reference to the time dependence of chemical reactions and then the dissolution path calculation refer to the irreversible dissolution of reactants and reversible precipitation of products ([1] to [4]). The system evolution is followed according to the reaction progress ξ which has been introduced in chemical system by Gibbs. Since few years, the experimental studies on the kinetics of minerals dissolution have allowed to take into account of dissolution rates data for the major minerals (silicates, carbonates...). More recently, a new geochemical codes generation appears based on thermodynamic potential and kinetic laws ([5] to [8]). The system evolution is followed according to the reaction time. (authors). 8 figs., 4 tabs., 24 refs

Geochemical characteristics of peat from two raised bogs of Germany

Science.gov (United States)

Mezhibor, A. M.

2016-11-01

Peat has a wide range of applications in different spheres of human activity, and this is a reason for a comprehensive study. This research represents the results of an ICP-MS study of moss and peat samples from two raised bogs of Germany. Because of the wide use of sphagnum moss and peat, determining their geochemical characteristics is an important issue. According to the results obtained, we can resume that the moss samples from Germany are rich in Cu, As, Y, Zr, Nb, and REE. The geochemical composition of the bogs reflects the regional environmental features and anthropogenic influence.

Defining and modeling the soil geochemical background of heavy metals from the Hengshi River watershed (southern China): Integrating EDA, stochastic simulation and magnetic parameters

International Nuclear Information System (INIS)

Zhou Xu; Xia Beicheng

2010-01-01

It is crucial to separate the soil geochemical background concentrations from anthropogenic anomalies and to provide a realistic environmental geochemical map honoring the fluctuations in original data. This study was carried out in the Hengshi River watershed, north of Guangdong, China and the method proposed combined exploratory data analysis (EDA), sequential indicator co-simulation (SIcS) and the ratio of isothermal remnant magnetization (S 100 = -IRM -100mT /SIRM). The results showed that this is robust procedure for defining and mapping soil geochemical background concentrations in mineralized regions. The rock magnetic parameter helps to improve the mapping process by distinguishing anthropogenic influences. In this study, the geochemical backgrounds for four potentially toxic heavy metals (copper 200 mg/kg; zinc 230 mg/kg; lead 190 mg/kg and cadmium 1.85 mg/kg) Cu, Zn and Cd exceeded the soil Grade II limits (for pH < 6.5) from the Chinese Environmental Quality Standard for Soils (GB 15618-1995) (EQSS) which are 100, 200, 250 and 0.3 mg/kg for Cu, Zn, Pb and Cd, respectively. In particular, the geochemical background level for Cd exceeds standard six times. Results suggest that local public health is at high-risk along the riparian region of the Hengshi River, although the watershed ecosystem has not been severely disturbed.

Leaching of APC residues from secondary Pb metallurgy using single extraction tests: the mineralogical and the geochemical approach.

Science.gov (United States)

Ettler, Vojtech; Mihaljevic, Martin; Sebek, Ondrej; Strnad, Ladislav

2005-05-20

Two air-pollution-control (APC) residues--one from flue gas cooling with alkaline water and one from deionized water cooling--from secondary lead metallurgy were submitted to two different standardized short-term leaching protocols: US EPA toxicity characteristic leaching procedure (TCLP) and static leaching according to Czech/European norm EN 12457-2. The experimental procedure was coupled with detailed mineralogical investigation of the solid material (SEM, XRPD) and speciation-solubility calculations using the PHREEQC-2 geochemical code. Both types of residues were considered as hazardous materials exhibiting substantial leaching of Pb (up to 7130 mg/l) and other inorganic contaminants. However, the APC residue produced by flue gas cooling with alkaline water (sample B) exhibits more favourable leaching and environmental characteristics than that produced by simple deionised water cooling (sample A). At pH 6, phosgenite (PbCl2.PbCO3) became the dominant secondary phase. The results are consistent with the mineralogical and geochemical studies focused on acidic forest soils highly polluted by smelter emissions, where anglesite, as a unique Pb-bearing phase, has been detected. From the technological point of view, the mixing of APC residue with alkaline water, followed by an increase in the suspension pH and equilibration with atmospheric CO2, may be used to ensure the precipitation of less soluble Pb carbonates, which are more easily recycled in the Pb recovery process in the metallurgical plant.

EQ3/6 geochemical modeling task plan for Nevada Nuclear Waste Storage Investigations (NNWSI)

Energy Technology Data Exchange (ETDEWEB)

Isherwood, D.; Wolery, T.

1984-04-10

This task plan outlines work needed to upgrade the EQ3/6 geochemical code and expand the supporting data bases to allow the Nevada Nuclear Waste Storage Investigations (NNWSI) to model chemical processes important to the storage of nuclear waste in a tuff repository in the unsaturated zone. The plan covers the fiscal years 1984 to 1988. The scope of work includes the development of sub-models in the EQ3/6 code package for studying the effects of sorption, precipitation kinetics, redox disequilibrium, and radiolysis on radionuclide speciation and solubility. The work also includes a glass/water interactions model and a geochemical flow model which will allow us to study waste form leaching and reactions involving the waste package. A special emphasis is placed on verification of new capabilities as they are developed and code documentation to meet NRC requirements. Data base expansion includes the addition of elements and associated aqueous species and solid phases that are specific to nuclear waste (e.g., actinides and fission products) and the upgrading and documentation of the thermodynamic data for other species of interest.

Application of integrated Landsat, geochemical and geophysical data in mineral exploration

International Nuclear Information System (INIS)

Conradsen, K.; Nilsson, G.; Thyrsted, T.; Gronlands Geologiske Undersogelse, Copenhagen, Denmark)

1985-01-01

In South Greenland (20000 sq. km) a remote sensing investigation is executed in connection with uranium exploration. The investigation includes analysis of Landsat data, conversion of geological, geochemical and geophysical data to image format compatible with Landsat images, and analysis of the total set of integrated data. The available geochemical data consisted of samples from 2000 sites, analyzed for U, K, Rb, Sr, Nb, Ga, Y, and Fe. The geophysical data comprised airborne gamma-spectrometric measurements and aeromagnetic data. The interpolation routines consisted of a kriging procedure for the geochemical data and a minimum curvature routine for the geophysical data. The analysis of the integrated data set is at a preliminary stage. As example a composite image showing Landsat channel 7, magnetic values, and Fe values as respectively intensity, hue and saturation is analyzed. It reveals alkaline intrusions and basaltic layers as anomalies while other anomalies cannot be accounted for on the basis of the present geological knowledge. 12 references

Coupled processes of fluid flow, solute transport, and geochemical reactions in reactive barriers

Energy Technology Data Exchange (ETDEWEB)

Kim, Jeongkon; Schwartz, Franklin W.; Xu, Tianfu; Choi, Heechul, and Kim, In S.

2004-01-02

A complex pattern of coupling between fluid flow and mass transport develops when heterogeneous reactions occur. For instance, dissolution and precipitation reactions can change a porous medium's physical properties, such as pore geometry and thus permeability. These changes influence fluid flow, which in turn impacts the composition of dissolved constituents and the solid phases, and the rate and direction of advective transport. Two-dimensional modeling studies using TOUGHREACT were conducted to investigate the coupling between flow and transport developed as a consequence of differences in density, dissolution precipitation, and medium heterogeneity. The model includes equilibrium reactions for aqueous species, kinetic reactions between the solid phases and aqueous constituents, and full coupling of porosity and permeability changes resulting from precipitation and dissolution reactions in porous media. In addition, a new permeability relationship is implemented in TOUGHREACT to examine the effects of geochemical reactions and density difference on plume migration in porous media. Generally, the evolutions in the concentrations of the aqueous phase are intimately related to the reaction-front dynamics. Plugging of the medium contributed to significant transients in patterns of flow and mass transport.

Fuzzy control of pressurizer dynamic process

International Nuclear Information System (INIS)

Ming Zhedong; Zhao Fuyu

2006-01-01

Considering the characteristics of pressurizer dynamic process, the fuzzy control system that takes the advantages of both fuzzy controller and PID controller is designed for the dynamic process in pressurizer. The simulation results illustrate this type of composite control system is with better qualities than those of single fuzzy controller and single PID controller. (authors)

Principal aquifers can contribute radium to sources of drinking water under certain geochemical conditions

Science.gov (United States)

Szabo, Zoltan; Fischer, Jeffrey M.; Hancock, Tracy Connell

2012-01-01

What are the most important factors affecting dissolved radium concentrations in principal aquifers used for drinking water in the United States? Study results reveal where radium was detected and how rock type and chemical processes control radium occurrence. Knowledge of the geochemical conditions may help water-resource managers anticipate where radium may be elevated in groundwater and minimize exposure to radium, which contributes to cancer risk. Summary of Major Findings: * Concentrations of radium in principal aquifers used for drinking water throughout the United States generally were below 5 picocuries per liter (pCi/L), the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) for combined radium - radium-226 (Ra-226) plus radium-228 (Ra-228) - in public water supplies. About 3 percent of sampled wells had combined radium concentrations greater than the MCL. * Elevated concentrations of combined radium were more common in groundwater in the eastern and central United States than in other regions of the Nation. About 98 percent of the wells that contained combined radium at concentrations greater than the MCL were east of the High Plains. * The highest concentrations of combined radium were in the Mid-Continent and Ozark Plateau Cambro-Ordovician aquifer system and the Northern Atlantic Coastal Plain aquifer system. More than 20 percent of sampled wells in these aquifers had combined radium concentrations that were greater than or equal to the MCL. * Concentrations of Ra-226 correlated with those of Ra-228. Radium-226 and Ra-228 occur most frequently together in unconsolidated sand aquifers, and their presence is strongly linked to groundwater chemistry. * Three common geochemical factors are associated with the highest radium concentrations in groundwater: (1) oxygen-poor water, (2) acidic conditions (low pH), and (3) high concentrations of dissolved solids.

Thermodynamic Data for Geochemical Modeling of Carbonate Reactions Associated with CO2 Sequestration – Literature Review

Energy Technology Data Exchange (ETDEWEB)

Krupka, Kenneth M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Cantrell, Kirk J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McGrail, B. Peter [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2010-09-01

Permanent storage of anthropogenic CO2 in deep geologic formations is being considered as a means to reduce the concentration of atmospheric CO2 and thus its contribution to global climate change. To ensure safe and effective geologic sequestration, numerous studies have been completed of the extent to which the CO2 migrates within geologic formations and what physical and geochemical changes occur in these formations when CO2 is injected. Sophisticated, computerized reservoir simulations are used as part of field site and laboratory CO2 sequestration studies. These simulations use coupled multiphase flow-reactive chemical transport models and/or standalone (i.e., no coupled fluid transport) geochemical models to calculate gas solubility, aqueous complexation, reduction/oxidation (redox), and/or mineral solubility reactions related to CO2 injection and sequestration. Thermodynamic data are critical inputs to modeling geochemical processes. The adequacy of thermodynamic data for carbonate compounds has been identified as an important data requirement for the successful application of these geochemical reaction models to CO2 sequestration. A review of thermodynamic data for CO2 gas and carbonate aqueous species and minerals present in published data compilations and databases used in geochemical reaction models was therefore completed. Published studies that describe mineralogical analyses from CO2 sequestration field and natural analogue sites and laboratory studies were also reviewed to identify specific carbonate minerals that are important to CO2 sequestration reactions and therefore require thermodynamic data. The results of the literature review indicated that an extensive thermodynamic database exists for CO2 and CH4 gases, carbonate aqueous species, and carbonate minerals. Values of ΔfG298° and/or log Kr,298° are available for essentially all of these compounds. However, log Kr,T° or heat capacity values at temperatures above 298 K exist for less than

Multielement geochemical reconnaissance for uranium in the Palmyrides region of central Syria

International Nuclear Information System (INIS)

Jubeli, Y.M.; Hale, M.

1988-01-01

Multielement reconnaissance geochemistry coupled with ground scintillation gamma ray measurements has been used to investigate the dispersion patterns of uranium and other major and trace elements in the arid Palmyrides region of central Syria. Over 500 geochemical samples of outcropping rock, wadi and playa sediments, overburden and groundwaters were taken over an area of approximately 9000 sq km. Most samples were analyzed for 25 major and trace elements by nebulization ICPAES; for As, Sb, Bi and Se by hydride generation and ICPAES; and for U, Th and La and other REE by neutron activation analysis. The resulting data were interpreted with the aid of univariate and multivariate statistical methods. The areal distributions of U, its associated elements, multivariate geochemical functions and factor scores were mapped using computer graphics. Results of the factor analysis indicate that the primary lithogeochemical dispersion patterns of uranium and associated elements are controlled by a combination of structural, lithological and environmental factors. Uranium and associated elements have subsequently been leached out of the phosphorite and other U enriched clayey limestones and carbonate rocks into the hydro- geologic regime. Redistribution of these elements is taking place along fracture zones and major faults. A degree of urnaium accumulation in a Neogene aquifer of the Ad-Daww basin is evident

Basic concepts and formulations for isotope geochemical modelling of groundwater systems

International Nuclear Information System (INIS)

Kalin, R.M.

1996-01-01

This chapter describes the basic chemical principles and methodologies for geochemical models and their use in the field of isotope hydrology. Examples of calculation procedures are given on actual field data. Summary information on available PC software for geochemical modeling is included. The specific software, NETPATH, which can be used for chemical speciation, mass balance and isotope balance along a flow path in groundwater systems, is discussed at some length with an illustrative example of its application to field data. (author). Refs, 14 figs, 15 tabs

Basic concepts and formulations for isotope geochemical modelling of groundwater systems

Energy Technology Data Exchange (ETDEWEB)

Kalin, R M [The Queen` s University, Belfast, Northern Ireland (United Kingdom). Dept. of Civil Engineering

1996-10-01

This chapter describes the basic chemical principles and methodologies for geochemical models and their use in the field of isotope hydrology. Examples of calculation procedures are given on actual field data. Summary information on available PC software for geochemical modeling is included. The specific software, NETPATH, which can be used for chemical speciation, mass balance and isotope balance along a flow path in groundwater systems, is discussed at some length with an illustrative example of its application to field data. (author). Refs, 14 figs, 15 tabs.

Statistical Process Control for KSC Processing

Science.gov (United States)

Ford, Roger G.; Delgado, Hector; Tilley, Randy

1996-01-01

The 1996 Summer Faculty Fellowship Program and Kennedy Space Center (KSC) served as the basis for a research effort into statistical process control for KSC processing. The effort entailed several tasks and goals. The first was to develop a customized statistical process control (SPC) course for the Safety and Mission Assurance Trends Analysis Group. The actual teaching of this course took place over several weeks. In addition, an Internet version of the same course complete with animation and video excerpts from the course when it was taught at KSC was developed. The application of SPC to shuttle processing took up the rest of the summer research project. This effort entailed the evaluation of SPC use at KSC, both present and potential, due to the change in roles for NASA and the Single Flight Operations Contractor (SFOC). Individual consulting on SPC use was accomplished as well as an evaluation of SPC software for KSC use in the future. A final accomplishment of the orientation of the author to NASA changes, terminology, data format, and new NASA task definitions will allow future consultation when the needs arise.

Some methodical questions of study of vertical geochemical zoning of ore deposits

International Nuclear Information System (INIS)

Sochevanov, N.N.; Gorelova, E.K.

1975-01-01

Taking a hydrothermal uranium deposit as an example, the advisability of dividing ore-localizing structures (for the purpose of making a calculation for a single geochemical zonality) into five zones, a supra-, an upper, a central, a lower and an infra-ore one, has been shown. It is recommended to determine the place of elements in the geochemical zonality sequence by taking into account the productivity of their aureoles and the location of the centre of gravity of their reserves in the ore, supra- and infra-ore horizons. When considering the peculiarities of a zonality, it is irrational to take account of elements determined with an insufficient sensitivity as well as of low-contrast or unstable ones. When calculating tracer ratios the most contrasting data can be obtained by using the most distant elements in the geochemical zonality sequence

Hydro-geochemical modeling of subalpine urbanized area: geochemical characterization of the shallow and deep aquifers of the urban district of Como (first results).

Science.gov (United States)

Terrana, Silvia; Brunamonte, Fabio; Frascoli, Francesca; Ferrario, Maria Francesca; Michetti, Alessandro Maria; Pozzi, Andrea; Gambillara, Roberto; Binda, Gilberto

2016-04-01

One of the greatest environmental and social-economics threats is climate change. This topic, in the next few years, will have a significant impact on the availability of water resources of many regions. This is compounded by the strong anthropization of water systems that shows an intensification of conflicts for water resource exploitation. Therefore, it is necessary a sustainable manage of natural resources thorough knowledge of the hosting territories. The development of investigation and data processing methods are essential to reduce costs for the suitable use and protection of resources. Identify a sample area for testing the best approach is crucial. This research aims to find a valid methodology for the characterization, modeling and management of subalpine urban aquifers, and the urban district of Como appears perfect. The city of Como is located at the southern end of the western sector of Lake Como (N Italy). It is a coastal town, placed on a small alluvial plain, therefore in close communication with the lake. The plain is drained by two streams, which are presently artificially buried, and have an underground flow path in the urban section till the mouth. This city area, so, is suitable for this project as it is intensely urbanized, its dimensions is not too extensive and it is characterized by two aquifers very important and little known. These are a shallow aquifer and a deep aquifer, which are important not only for any water supply, but also for the stability of the ground subsidence in the city. This research is also the opportunity to work in a particular well-known area with high scientific significance; however, there is complete absence of information regarding the deep aquifer. Great importance has also the chosen and used of the more powerful open source software for this type of area, such as PHREEQC, EnvironInsite, PHREEQE etc., used for geological and geochemical data processing. The main goal of this preliminary work is the

Control system for technological processes in tritium processing plants with process analysis

International Nuclear Information System (INIS)

Retevoi, Carmen Maria; Stefan, Iuliana; Balteanu, Ovidiu; Stefan, Liviu; Bucur, Ciprian

2005-01-01

Integration of a large variety of installations and equipment into a unitary system for controlling the technological process in tritium processing nuclear facilities appears to be a rather complex approach particularly when experimental or new technologies are developed. Ensuring a high degree of versatility allowing easy modifications in configurations and process parameters is a major requirement imposed on experimental installations. The large amount of data which must be processed, stored and easily accessed for subsequent analyses imposes development of a large information network based on a highly integrated system containing the acquisition, control and technological process analysis data as well as data base system. On such a basis integrated systems of computation and control able to conduct the technological process could be developed as well protection systems for cases of failures or break down. The integrated system responds to the control and security requirements in case of emergency and of the technological processes specific to the industry that processes radioactive or toxic substances with severe consequences in case of technological failure as in the case of tritium processing nuclear plant. In order to lower the risk technological failure of these processes an integrated software, data base and process analysis system are developed, which, based on identification algorithm of the important parameters for protection and security systems, will display the process evolution trend. The system was checked on a existing plant that includes a removal tritium unit, finally used in a nuclear power plant, by simulating the failure events as well as the process. The system will also include a complete data base monitoring all the parameters and a process analysis software for the main modules of the tritium processing plant, namely, isotope separation, catalytic purification and cryogenic distillation

Hydrocarbon degassing of the earth and origin of oil-gas fields (isotope-geochemical and geodynamic aspects)

Science.gov (United States)

Valyaev, Boris; Dremin, Ivan

2016-04-01

More than half a century ago, Academician PN Kropotkin substantiated the relationship of the formation and distribution of oil and gas fields with the processes of emanation hydrocarbon degassing of the Earth. Over the years, the concept of PN Kropotkin received further development and recognition of studies based on new factual material. Of particular importance are the following factors: a) the results of studies on global and regional uneven processes of traditional oil and gas and the role of deep faults in controlling the spread of oil and gas fields; b) the results of the research on gigantic volumes and localization of the discharges of hydrocarbon fluids (mud volcanoes, seeps) on land and into the atmosphere and through the bottom of the World ocean; c) the results of the studies on grand volumes of the spread of unconventional hydrocarbon resources in their non-traditional fields, especially on near-surface interval of unconventional oil and gas accumulation with gas hydrates, heavy oil and bitumen, as well as extraordinary resources of oil and gas in the shale and tight rocks. Deep mantle-crust nature of oil and gas in traditional and nontraditional deposits thus received further substantiation of geological and geophysical data and research results. However, isotopic and geochemical data are still interpreted in favor of the concept of the genesis of oil and gas in the processes of thermal catalytic conversion of organic matter of sedimentary rocks, at temperatures up to 200°C. In this report an alternative interpretation of the isotope carbon-hydrogen system (δ13C-δD) for gas and of oil deposits, isotope carbon system for methane and carbon dioxide (δ13C1-δ13C0) will be presented. An alternative interpretation will also be presented for the data on carbon-helium isotope geochemical system for oil and gas fields, volcanoes and mud volcanoes. These constructions agree with the geological data on the nature of deep hydrocarbon fluids involved in the

Major hydrogeochemical processes in an Acid Mine Drainage affected estuary

International Nuclear Information System (INIS)

Asta, Maria P.; Calleja, Maria Ll.; Pérez-López, Rafael; Auqué, Luis F.

2015-01-01

Highlights: • Mixing of acid riverine water with alkaline seawater was studied in an estuary. • Combination of data and geochemical tools allowed modeling the water mixing. • The main geochemical processes were identified and for the first time quantified. • Water chemistry is the result of mixing, dissolution-precipitation and sorption. • Main reactions: gypsum and calcite dissolution and Al and Fe solids precipitation. - Abstract: This study provides geochemical data with the aim of identifying and quantifying the main processes occurring in an Acid Mine Drainage (AMD) affected estuary. With that purpose, water samples of the Huelva estuary were collected during a tidal half-cycle and ion–ion plots and geochemical modeling were performed to obtain a general conceptual model. Modeling results indicated that the main processes responsible for the hydrochemical evolution of the waters are: (i) the mixing of acid fluvial water with alkaline ocean water; (ii) precipitation of Fe oxyhydroxysulfates (schwertmannite) and hydroxides (ferrihydrite); (iii) precipitation of Al hydroxysulfates (jurbanite) and hydroxides (amorphous Al(OH) 3 ); (iv) dissolution of calcite; and (v) dissolution of gypsum. All these processes, thermodynamically feasible in the light of their calculated saturation states, were quantified by mass-balance calculations and validated by reaction-path calculations. In addition, sorption processes were deduced by the non-conservative behavior of some elements (e.g., Cu and Zn)

Welding process modelling and control

Science.gov (United States)

Romine, Peter L.; Adenwala, Jinen A.

1993-01-01

The research and analysis performed, and software developed, and hardware/software recommendations made during 1992 in development of the PC-based data acquisition system for support of Welding Process Modeling and Control is reported. A need was identified by the Metals Processing Branch of NASA Marshall Space Flight Center, for a mobile data aquisition and analysis system, customized for welding measurement and calibration. Several hardware configurations were evaluated and a PC-based system was chosen. The Welding Measurement System (WMS) is a dedicated instrument, strictly for the use of data aquisition and analysis. Although the WMS supports many of the functions associated with the process control, it is not the intention for this system to be used for welding process control.

Genesis and evolution of the fumaroles of vulcano (Aeolian Islands, Italy): a geochemical model

Science.gov (United States)

Carapezza, M.; Nuccio, P. M.; Valenza, M.

1981-09-01

A geochemical model explaining the presence of fumaroles having different gas composition and temperature at the top of the crater and along the northeastern coast of Vulcano island is proposed. A pressurized biphase (liquid-vapor) reservoir at the depth of about 2 km is hypothesized. Energy and mass balance sheets control P-T conditions in the system. P-T must vary along a boiling curve of brine as liquid is present. The CO2 content in the steam is governed by the thermodynamic properties of the fluids in the H2-NaCl-CO2 system. On the assumption that oxygen fugacity in the system is between the HM-FMQ oxygen buffers, observed SO2/H2S, CO2/CO, CO/CH4 ratios in the fumarolic gases at the Fossa crater appear in equilibrium with a temperature higher than that observed, such as may exist at depth. The more reduced gas phases present on the sea-side may result from re-equilibrium processes in shallower aquifers. The suggested model would help in monitoring changes in volcanic activity by analyzing fumarolic gases.

Variation and Control of Process Behavior

International Nuclear Information System (INIS)

Pawlicki, Todd; Whitaker, Matthew

2008-01-01

The purpose of this work was to highlight the importance of controlling process variability for successful quality assurance (QA). We describe the method of statistical process control for characterizing and controlling a process. Traditionally, QA has been performed by comparing some important measurement (e.g., linear accelerator output) against a corresponding specification. Although useful in determining the fitness of a particular measurement, this approach does not provide information about the underlying process behavior over time. A modern view of QA is to consider the time-ordered behavior of a process. Every process displays characteristic behaviors that are independent of the specifications imposed on it. The goal of modern QA is, not only to ensure that a process is on-target, but that it is also operating with minimal variation. This is accomplished by way of a data-driven approach using process behavior charts. The development of process behavior charts, historically known as control charts, and process behavior (action) limits are described. The effect these concepts have on quality management is also discussed

Science-based information processing in the process control of power stations

International Nuclear Information System (INIS)

Weisang, C.

1992-01-01

Through the application of specialized systems, future-orientated information processing integrates the sciences of processes, control systems, process control strategies, user behaviour and ergonomics. Improvements in process control can be attained, inter alia, by the preparation of the information contained (e.g. by suppressing the flow of signals and replacing it with signals which are found on substance) and also by an ergonomic representation of the study of the process. (orig.) [de

Geochemical characterization of the siliciclastic rocks of Chitravati ...

Indian Academy of Sciences (India)

V Somasekhar

2018-05-23

May 23, 2018 ... Chitravati Group of Cuddapah Supergroup to decipher the provenance and depositional environment. Both the units ... Based on major element geochemical classification diagram, Pulivendla Quartzite .... The youngest age limit of the Nallamalai ...... eastern Oregon and western Idaho, USA: Implications for.

Uruguay Mining inventory. Florida fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Florida fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 752 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

Study of the coupling of geochemical models based on thermodynamic equilibrium with models of component transfer as solutions in porous media or fractures

International Nuclear Information System (INIS)

Coudrain-Ribstein, A.

1985-01-01

This study is a contribution of analyses possibilities of modelling the transfer of components in the underground taking into account complexes geochemical phenomena. In the first part, the aim and the methodology of existing codes are presented. The transfer codes describe with a great precision the physical phenomena of transport but they are based on a very simple conceptualisation of the geochemical phenomena of retention by the rock. The geochemical models are interested by a stable unity of volume. They allow to compute the equilibrium distribution of the components between the chemical species of the solution, and the solid and gaseous phases. They use important thermodynamic data bases corresponding to each possible reaction. To sum up the situation about the geochemical codes in Europe and United States, a list of about thirty codes describe their method and potentialities. The mathematical analysis of the different methods used in both types of codes is presented. Then, the principles of a modelisation associating the potentialities of the transport codes and the geochemical codes are discussed. It is not possible to think of a simple coupling. A general code must be established on the bases of the existing codes but also on new concepts and under new constraints. In such studies one must always deal with the problem of the reactions kinetics. When the velocity of the reactions is big enough versus the velocity of transport processes, the assumption of local geochemical equilibrium can be retained. A general code would be very cumbersome, expensive and difficult to use. The results would be difficult to analyse and exploit. On the other hand, for each case study, a detailed analysis can point out many computing simplifications without simplifying the concepts [fr

Performance of a Zerovalent Iron Reactive Barrier for the Treatment of Arsenic in Groundwater: Part 2. Geochemical Modeling and Solid Phase Studies

Science.gov (United States)

Arsenic uptake processes were evaluated in a zerovalent iron reactive barrier installed at a lead smelting facility using geochemical modeling, solid-phase analysis, and X-ray absorption spectroscopy techniques. Aqueous speciation of arsenic plays a key role in directing arsenic...

Uruguay mining Inventory: Geochemical prospecting results of Valentines mapping

International Nuclear Information System (INIS)

Spangenberg, J.; Filippini, J.

1985-01-01

This work is about geochemical prospecting carried out into the Uruguay mining inventory framework. In this case the survey was in Valentines mapping. Florida, Durazno and Treinta y Tres provinces of Uruguay .

Modern Processes of Hydrocarbon Migration and Re-Formation of Oil and Gas Fields (Based on the Results of Monitoring and Geochemical Studies)

Science.gov (United States)

Plotnikova, Irina; Salakhidinova, Gulmira; Nosova, Fidania; Pronin, Nikita; Ostroukhov, Sergey

2015-04-01

Special geochemical studies of oils allowed to allocate a movable migration component of oils in the industrial oil deposits. In the field the migration component of oils varies in different parts of the field. The largest percentage of the light migration component (gas condensate of the oil) was detected in the central part of the Kama-Kinel troughs system. Monitoring of the composition of water, oil and gas (condensate light oil component) in the sedimentary cover and ni crystalline basement led to the conclusion of modern migration of hydrocarbons in sedimentary cover. This proves the existence of the modern processes of formation and reformation of oil and gas fields. This presentation is dedicated to the problem of definition of geochemical criteria of selection of hydrocarbons deposit reformation zone in the sample wells of Minibaevskaya area of Romashkinskoye field. While carrying out this work we examined 11 samples of oil from the Upper Devonian Pashiysky horizon. Four oil samples were collected from wells reckoned among the "anomalous" zones that were marked out according to the results of geophysical, oil field and geological research. Geochemical studies of oils were conducted in the laboratory of geochemistry of the Kazan (Volga-region) Federal University. The wells where the signs of hydrocarbons influx from the deep zones of the crust were recorded are considered to be "anomalous". A number of scientists connect this fact to the hypothesis about periodic influx of deep hydrocarbons to the oil deposits of Romashkinskoye field. Other researchers believe that the source rocks of the adjacent valleys sedimentary cover generate gases when entering the main zone of gas formation, which then migrate up the section and passing through the previously formed deposits of oil, change and "lighten" their composition. Regardless of the point of view on the source of the hydrocarbons, the study of the process of deposits refilling with light hydrocarbons is an

Analysis on geochemical conditions of uranium mineralization in Bashibulake uranium deposit, Xinjiang

International Nuclear Information System (INIS)

Liu Zhangyue; Dong Wenming; Cai Genqing; Liu Hongxu; Deng Huabo

2011-01-01

By studying the palaeoclimate and metallogenesis related geochemical indexes, this paper proposes that the hosting rocks should form in geochemical oxidation setting under arid palaeoclimate. The study on element assemblage associated with uranium mineralization indicates that the target hosting rocks suffered from different degrees of reworking of reducing fluid at first and then being superimposed by supergene oxidative fluid at tectonic uplifting stage. The uranium mineralization is located in reworked and superimposed places of two types of fluid. (authors)

Geochemical conditions and the occurrence of selected trace elements in groundwater basins used for public drinking-water supply, Desert and Basin and Range hydrogeologic provinces, 2006-11: California GAMA Priority Basin Project

Science.gov (United States)

Wright, Michael T.; Fram, Miranda S.; Belitz, Kenneth

2015-01-01

The geochemical conditions, occurrence of selected trace elements, and processes controlling the occurrence of selected trace elements in groundwater were investigated in groundwater basins of the Desert and Basin and Range (DBR) hydrogeologic provinces in southeastern California as part of the Priority Basin Project (PBP) of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA PBP is designed to provide an assessment of the quality of untreated (raw) groundwater in the aquifer systems that are used for public drinking-water supply. The GAMA PBP is being conducted by the California State Water Resources Control Board in collaboration with the U.S. Geological Survey and the Lawrence Livermore National Laboratory.

Investigation of Geochemical Characteristics and Controlling Processes of Groundwater in a Typical Long-Term Reclaimed Water Use Area

Directory of Open Access Journals (Sweden)

Yong Xiao

2017-10-01

Full Text Available The usage of reclaimed water can efficiently mitigate water crises, but it may cause groundwater pollution. To clearly understand the potential influences of long-term reclaimed water usage, a total of 91 samples of shallow and deep groundwater were collected from a typical reclaimed water use area during the dry and rainy seasons. The results suggest both shallow and deep groundwater are mainly naturally alkaline freshwater, which are composed mainly of Ca-HCO3, followed by mixed types such as Ca-Na-HCO3 and Ca-Mg-HCO3. A seasonal desalination trend was observed in both shallow and deep aquifers due to dilution effects in the rainy season. Groundwater chemical compositions in both shallow and deep aquifers are still dominantly controlled by natural processes such as silicate weathering, minerals dissolution and cation exchange. Human activities are also the factors influencing groundwater chemistry. Urbanization has been found responsible for the deterioration of groundwater quality, especially in shallow aquifers, because of the relative thin aquitard. Reclaimed water usage for agricultural irrigation and landscape purposes has nearly no influences on groundwater quality in rural areas due to thick aquitards. Therefore, reclaimed water usage should be encouraged in arid and semiarid areas with proper hydrogeological condition.

The geochemical chararateristics of the marble deposits east of ...

African Journals Online (AJOL)

), marbles were investigated with the view to establishing marble occurrences and their geochemical characteristics. Crystalline rocks of the Nigerian Basement Complex (migmatite – gneiss complex) underlie the area. Ten marble bodies were ...

Supporting Cross-Organizational Process Control

Science.gov (United States)

Angelov, Samuil; Vonk, Jochem; Vidyasankar, Krishnamurthy; Grefen, Paul

E-contracts express the rights and obligations of parties through a formal, digital representation of the contract provisions. In process intensive relationships, e-contracts contain business processes that a party promises to perform for the counter party, optionally allowing monitoring of the execution of the promised processes. In this paper, we describe an approach in which the counter party is allowed to control the process execution. This approach will lead to more flexible and efficient business relations which are essential in the context of modern, highly dynamic and complex collaborations among companies. We present a specification of the process controls available to the consumer and their support in the private process specification of the provider.

Processes subject to integrated pollution control. Petroleum processes: oil refining and associated processes

International Nuclear Information System (INIS)

1995-01-01

This document, part of a series offering guidance on pollution control regulations issued by Her Majesty's Inspectorate of Pollution, (HMIP) focuses on petroleum processes such as oil refining and other associated processes. The various industrial processes used, their associated pollution release routes into the environment and techniques for controlling these releases are all discussed. Environmental quality standards are related to national and international agreements on pollution control and abatement. HMIP's work on air, water and land pollution monitoring is also reported. (UK)

Comparison of thermodynamic databases used in geochemical modelling

International Nuclear Information System (INIS)

Chandratillake, M.R.; Newton, G.W.A.; Robinson, V.J.

1988-05-01

Four thermodynamic databases used by European groups for geochemical modelling have been compared. Thermodynamic data for both aqueous species and solid species have been listed. When the values are directly comparable any differences between them have been highlighted at two levels of significance. (author)

Uruguay Mining inventory. Minas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Minas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 380 km2 obtaining with 433 samples for study which were analized by Plasma Emission Spectrometry in Orleans BRGM laboratories

Applicability of statistical process control techniques

NARCIS (Netherlands)

Schippers, W.A.J.

1998-01-01

This paper concerns the application of Process Control Techniques (PCTs) for the improvement of the technical performance of discrete production processes. Successful applications of these techniques, such as Statistical Process Control Techniques (SPC), can be found in the literature. However, some

Neutron activation analysis of geochemical samples

International Nuclear Information System (INIS)

Rosenberg, R.; Zilliacus, R.; Kaistila, M.

1983-06-01

The present paper will describe the work done at the Technical Research Centre of Finland in developing methods for the large-scale activation analysis of samples for the geochemical prospecting of metals. The geochemical prospecting for uranium started in Finland in 1974 and consequently a manually operated device for the delayed neutron activation analysis of uranium was taken into use. During 1974 9000 samples were analyzed. The small capacity of the analyzer made it necessary to develop a completely automated analyzer which was taken into use in August 1975. Since then 20000-30000 samples have been analyzed annually the annual capacity being about 60000 samples when running seven hours per day. Multielemental instrumental neutron activation analysis is used for the analysis of more than 40 elements. Using instrumental epithermal neutron activation analysis 25-27 elements can be analyzed using one irradiation and 20 min measurement. During 1982 12000 samples were analyzed for mining companies and Geological Survey of Finland. The capacity is 600 samples per week. Besides these two analytical methods the analysis of lanthanoids is an important part of the work. 11 lanthanoids have been analyzed using instrumental neutron activation analysis. Radiochemical separation methods have been developed for several elements to improve the sensitivity of the analysis

Soil Iodine Determination in Deccan Syneclise, India: Implications for Near Surface Geochemical Hydrocarbon Prospecting

International Nuclear Information System (INIS)

Mani, Devleena; Kumar, T. Satish; Rasheed, M. A.; Patil, D. J.; Dayal, A. M.; Rao, T. Gnaneshwar; Balaram, V.

2011-01-01

The association of iodine with organic matter in sedimentary basins is well documented. High iodine concentration in soils overlying oil and gas fields and areas with hydrocarbon microseepage has been observed and used as a geochemical exploratory tool for hydrocarbons in a few studies. In this study, we measure iodine concentration in soil samples collected from parts of Deccan Syneclise in the west central India to investigate its potential application as a geochemical indicator for hydrocarbons. The Deccan Syneclise consists of rifted depositional sites with Gondwana–Mesozoic sediments up to 3.5 km concealed under the Deccan Traps and is considered prospective for hydrocarbons. The concentration of iodine in soil samples is determined using ICP-MS and the values range between 1.1 and 19.3 ppm. High iodine values are characteristic of the northern part of the sampled region. The total organic carbon (TOC) content of the soil samples range between 0.1 and 1.3%. The TOC correlates poorly with the soil iodine (r 2 < 1), indicating a lack of association of iodine with the surficial organic matter and the possibility of interaction between the seeping hydrocarbons and soil iodine. Further, the distribution pattern of iodine compares well with two surface geochemical indicators: the adsorbed light gaseous hydrocarbons (methane through butane) and the propane-oxidizing bacterial populations in the soil. The integration of geochemical observations show the occurrence of elevated values in the northern part of the study area, which is also coincident with the presence of exposed dyke swarms that probably serve as conduits for hydrocarbon microseepage. The corroboration of iodine with existing geological, geophysical, and geochemical data suggests its efficacy as one of the potential tool in surface geochemical exploration of hydrocarbons. Our study supports Deccan Syneclise to be promising in terms of its hydrocarbon prospects.

Establishing geochemical background levels of selected trace elements in areas having geochemical anomalies: The case study of the Orbetello lagoon (Tuscany, Italy)

International Nuclear Information System (INIS)

Romano, Elena; Bergamin, Luisa; Croudace, Ian W.; Ausili, Antonella; Maggi, Chiara; Gabellini, Massimo

2015-01-01

The determination of background concentration values (BGVs) in areas, characterised by the presence of natural geochemical anomalies and anthropogenic impact, appears essential for a correct pollution assessment. For this purpose, it is necessary to establish a reliable method for determination of local BGVs. The case of the Orbetello lagoon, a geologically complex area characterized by Tertiary volcanism, is illustrated. The vertical concentration profiles of As, Cd, Cr, Cu, Hg, Ni, Pb and Zn were studied in four sediment cores. Local BGVs were determined considering exclusively samples not affected by anthropogenic influence, recognized by means of multivariate statistics and radiochronological dating ( 137 Cs and 210 Pb). Results showed BGVs well-comparable with mean crustal or shale values for most of the considered elements except for Hg (0.87 mg/kg d.w.) and As (16.87 mg/kg d.w.), due to mineralization present in the catchment basin draining into the lagoon. - Highlights: • Pollution assessment in areas with geochemical anomalies needs local reference values. • A new method for the determination of background values (BGV) was established. • Geochemical data from unpolluted samples of sediment cores were used. • Statistics and geochronology were applied to recognize unpolluted sediments. • Anthropogenically influenced samples were not considered for BGV determination. - A method including multivariate statistics and radiochronological dating is proposed for determining local background values for trace elements using analytical data form sediment cores

Microprocessors control of fermentation process

Energy Technology Data Exchange (ETDEWEB)

Fawzy, A S; Hinton, O R

1980-01-01

This paper presents three schemes for the solution of the optimal control of fermentation process. It also shows the advantages of using microprocessors in controlling and monitoring this process. A linear model of the system is considered. An optimal feedback controller is determined which maintains the states (substrate and organisms concentration) at desired values when the system is subjected to disturbances in the influent substrate and organisms concentration. Simulation results are presented for the three cases.

Reactivity of the calcite–water-interface, from molecular scale processes to geochemical engineering

International Nuclear Information System (INIS)

Heberling, Frank; Bosbach, Dirk; Eckhardt, Jörg-Detlef; Fischer, Uwe; Glowacky, Jens; Haist, Michael; Kramar, Utz; Loos, Steffen; Müller, Harald S.; Neumann, Thomas; Pust, Christopher; Schäfer, Thorsten; Stelling, Jan

2014-01-01

Highlights: • The current state of some aspects of calcite–water-interface chemistry is reviewed. • The interface structure is characterized at a molecular scale. • Experimental and theoretical studies on contaminant sorption at calcite are presented. • The influence of phosphonates on calcite growth is investigated. • The effect of limestone on the workability of cement suspensions is addressed. - Abstract: Surface reactions on calcite play an important role in geochemical and environmental systems, as well as many areas of industry. In this review, we present investigations of calcite that were performed in the frame of the joint research project “RECAWA” (reactivity of calcite–water-interfaces: molecular process understanding for technical applications). As indicated by the project title, work within the project comprised a large range of length scales. The molecular scale structure of the calcite (1 0 4)–water-interface is refined based on surface diffraction data. Structural details are related to surface charging phenomena, and a simplified basic stern surface complexation model is proposed. As an example for trace metal interactions with calcite surfaces we review and present new spectroscopic and macroscopic experimental results on Selenium interactions with calcite. Results demonstrate that selenate (SeO 4 2− ) shows no significant interaction with calcite at our experimental conditions, while selenite (SeO 3 2− ) adsorbs at the calcite surface and can be incorporated into the calcite structure. Atomistic calculations are used to assess the thermodynamics of sulfate (SO 4 2− ), selenate (SeO 4 2− ), and selenite (SeO 3 2− ) partitioning in calcite and aragonite. The results show that incorporation of these oxo-anions into the calcite structure is so highly endothermic that incorporation is practically impossible at bulk equilibrium and standard conditions. This indicates that entrapment processes are involved when

Association between product quality control and process quality control of bulk milk

NARCIS (Netherlands)

Velthuis, A.; Asseldonk, van M.A.P.M.

2010-01-01

Assessment of dairy-milk quality is based on product quality control (testing bulk-milk samples) and process quality control (auditing dairy farms). It is unknown whether process control improves product quality. To quantify possible association between product control and process control a

Process and apparatus for controlling control rods

International Nuclear Information System (INIS)

Gebelin, B.; Couture, R.

1987-01-01

This process and apparatus is characterized by 2 methods, for examination of cluster of nuclear control rods. Foucault current analyzer which examines fraction by fraction all the control rods. This examination is made by rotation of the cluster. Doubtful rods are then analysed by ultrasonic probe [fr

Geochemical prospecting for rare earth elements using termite mound materials

Science.gov (United States)

Horiuchi, Yu; Ohno, Tetsuji; Hoshino, Mihoko; Shin, Ki-Cheol; Murakami, Hiroyasu; Tsunematsu, Maiko; Watanabe, Yasushi

2014-12-01

The Blockspruit fluorite prospect, located in North West State of the Republic of South Africa, occurs within an actinolite rock zone that was emplaced into the Kenkelbos-type granite of Proterozoic age. There are a large number of termite mounds in the prospect. For geochemical prospecting for rare earth elements (REEs), in total, 200 samples of termite mound material were collected from actinolite rock and granite zones in the prospect. Geochemical analyses of these termite mound materials were conducted by two methods: portable X-ray fluorescence (XRF) spectrometry and inductively coupled plasma-mass spectrometry (ICP-MS). Comparison of the two methods broadly indicates positive correlations of REEs (La, Ce, Pr, Nd, and Y), in particular Y and La having a strong correlation. As the result of modal abundance analyses, the actinolite rock at surface mainly consists of ferro-actinolite (89.89 wt%) and includes xenotime (0.26 wt%) and monazite (0.21 wt%) grains as REE minerals. Termite mound materials from actinolite rock also contain xenotime (0.27 wt%) and monazite (0.41 wt%) grains. In addition, termite mound materials from the actinolite rock zone have high hematite and Fe silicate contents compared to those from granite zone. These relationships suggest that REE minerals in termite mound materials originate form actinolite rock. Geochemical anomaly maps of Y, La, and Fe concentrations drawn based on the result of the portable XRF analyses show that high concentrations of these elements trend from SW to NE which broadly correspond to occurrences of actinolite body. These results indicate that termite mounds are an effective tool for REE geochemical prospection in the study area for both light REEs and Y, but a more detailed survey is required to establish the distribution of the actinolite rock body.

Petrological and geochemical Highlights in the floating fragments of the October 2011 submarine eruption offshore El Hierro (Canary Islands): Relevance of submarine hydrothermal processes

Science.gov (United States)

Rodriguez-Losada, Jose A.; Eff-Darwich, Antonio; Hernandez, Luis E.; Viñas, Ronaldo; Pérez, Nemesio; Hernandez, Pedro; Melián, Gladys; Martinez-Frías, Jesús; Romero-Ruiz, M. Carmen; Coello-Bravo, Juan Jesús

2015-02-01

This paper describes the main physical, petrological and geochemical features of the floating fragments that were emitted in the initial stages of the 2011-2012 submarine eruption off the coast of the Canarian island of El Hierro, located 380 km from the Northwest African Coast. It attempts to assess the potential of radiometric analyses to discern the intriguing origin of the floating fragments and the differences between their constituent parts. In this regard, the material that conforms the core of the fragments contains the largest concentration of uranium (U) ever found in volcanic rocks of the Canary Islands. This enrichment in U is not found in the content of thorium (Th), hence the floating fragments have an unusual U/Th ratio, namely equal to or larger than 3. Although the origin of this material is under discussion, it is proposed that the enrichment in U is the result of hydrothermal processes.

An integrated geological, geochemical, and geophysical investigation of uranium metallogenesis in selected granitic plutons of the Miramichi Anticlinorium, New Brunswick

International Nuclear Information System (INIS)

Hassan, H.H.; McAllister, A.L.

1992-01-01

Integrated geological, geochemical, and geophysical data for the post-tectonic granitic rocks of the North Pole, Burnthill, Dungarvon, Trout Brook, and Rocky Brook plutons and surrounding areas were examined to assess their potential for uranium mineralization. Geological, geochemical, and geophysical criteria that are thought to be useful guides for uranium exploration were also established for the host granites. The granitic plutons were emplaced discordantly, late in the tectonomagmatic sequence and at shallow depths within the metasedimentary rocks of the Miramichi Anticlinorium. Geochemically, the host granites are highly evolved (Si0 2 > 75 wt. %), peraluminous and have strong similarities with ilmenite-series 'S-type' and 'A-type' granitoids. Uranium occurrences are spatially and perhaps temporally associated with late-phase differentiates of the plutons where elevated levels of other lithophile elements such as Sn, W, Mo, and F were also detected. Geophysically, the granitic plutons are associated with distinctively high aeroradiometric eU, eTh, and K anomalies that coincide with strong negative Bouguer anomalies and low magnetic values. Conceptual models involving magmatic and hydrothermal processes have been adopted to explain the concentration of uranium and associated metals in the granitic plutons

Third Dutch Process Security Control Event

NARCIS (Netherlands)

Luiijf, H.A.M.

2009-01-01

On June 4th, 2009, the third Dutch Process Control Security Event took place in Amsterdam. The event, organised by the Dutch National Infrastructure against Cybercrime (NICC), attracted both Dutch process control experts and members of the European SCADA and Control Systems Information Exchange

Mineralogical and geochemical studies of phosphorite nodules in ...

African Journals Online (AJOL)

Mineralogical and geochemical studies of phosphorite nodules in the Dange Formation Sokoto Basin, Northwestern Niveria. OA Adekeye, SO Akande. Abstract. No Abstract Available Journal of Mining and Geology Vol.40(2) 2004: 101-106. Full Text: EMAIL FULL TEXT EMAIL FULL TEXT · DOWNLOAD FULL TEXT ...

Geochemical assessment of light gaseous hydrocarbons in near ...

Indian Academy of Sciences (India)

Light hydrocarbons in soil have been used as direct indicators in geochemical hydrocarbon exploration, which remains an unconventional path in the petroleum industry. The occurrence of adsorbed soil ... Kalpana1 D J Patil1 A M Dayal1. National Geophysical Research Institute, Uppal Road, Hyderabad 500606, India.

Control measurement system in purex process

International Nuclear Information System (INIS)

Mani, V.V.S.

1985-01-01

The dependence of a bulk facility handling Purex Process on the control measurement system for evaluating the process performance needs hardly be emphasized. process control, Plant control, inventory control and quality control are the four components of the control measurement system. The scope and requirements of each component are different and the measurement methods are selected accordingly. However, each measurement system has six important elements. These are described in detail. The quality assurance programme carried out by the laboratory as a mechanism through which the quality of measurements is regularly tested and stated in quantitative terms is also explained in terms of internal and external quality assurance, with examples. Suggestions for making the control measurement system more responsive to the operational needs in future are also briefly discussed. (author)

Application of the PHREEQC geochemical computer model during the design and operation of UK mine water treatment schemes

Energy Technology Data Exchange (ETDEWEB)

Croxford, S.J.; England, A.; Jarvis, A.P. [IMC White Young Green Engineering and Environment, Sutton-in-Ashfield (United Kingdom)

2004-07-01

The UK Coal Authority operates more than 20 full-scale mine water treatment schemes. The PHREEQC geochemical model has been used during the design and operation of two of the UK Coal Authority's treatment systems to assess whether it is possible to more accurately predict the fate and behaviour of contaminants through the treatment process. These systems are at Frances Colliery, Fife, Scotland, and at Horden Colliery, County Durham, England. The characteristics of the mine water at these sites, and the treatment systems installed to remediate them, are described. At Frances Colliery the following issues have been investigated using the PHREEQC model: determination of optimum alkali dose rate; and investment of secondary mineralization that causes pipe fouling. At Horden Colliery areas investigated using the PHREEQC model are: prediction of sludge volume production for various alkali reagents; predication of the influence of elevated carbon dioxide partial pressures on alkali requirements; and influence of elevated chloride concentration on sludge characteristics and production. The results of the investigation are presented and discussed. The study suggests that geochemical modelling may be a useful tool in determining both the geochemical processes occurring within a mine water treatment system and ultimately the likely costs involved during the operation of a particular scheme. Plans for future work include further validation of the PHREEQC model predictions by careful sampling and analysis of water chemistry and secondary mineral phases through the treatment systems. In the future it is hoped that the PHREEQC model may become a useful tool in the design phase of mine water treatment systems. 7 refs., 8 tabs.

Geological and Geochemical Criteria for the Estimation of the Area of The Lesser Hinggan for the Endogenous Gold Mineralization (The Far East, Russia)

Science.gov (United States)

Yurchenko, Yuriy

2015-04-01

The Area of the Lesser Hinggan in the middle of the XIX century has been known as one of the Gold areas of the Far East. Exploration of gold in different years were engaged by P.K. Yavorovskiy (1904), E.E. Anert (1928), G.V. Itsikson (1961), V.A. Buryak (1999, 2002, 2003), A.M. Zhirnov (1998, 2000, 2008), L.V. Eyrish (1960, 1964, 1995, 1999, 2002, 2008) and many others. But despite the abundance of factual materials in the problem of the gold metallogeny of the Lesser Hinggan are more aspects that still have not received a answer. Among them is the key issue about indigenous sources of the gold. First for the Lesser Hinggan area, structural-geochemical zoning at 1:200 000 scale was carried out based on the results of the precise analyses of over 2,600 soil and sediment stream samples. Three anomalous geochemical zones and nine anomalous geochemical clusters in their contours specialized for gold mineralization were revealed. Regional clarkes (fersms) for 19 chemical elements were calculated. Geological formations geochemically specialized for gold and their role in endogenous ore-forming processes were defined. Geochemical criteria for endogenous gold mineralization and its ore-formational affiliation were defined as well. Thus, from the geological and geochemical data, are the following signs of the gold mineralization of the Lesser Hinggan: 1. Some geological formations are geochemical specialized by the gold (carbon ("black") schists and ferruginous quartzite Vendian-Cambrian Hinggan series). They're considered as a source of the gold, involved in younger epigenetic processes of mobilization and redistribution of this element; 2. Contrasting geochemical anomalies of the gold and elements satellites in the secondary halos and stream sediments displayed in the contours of the geological formations of a wide age range - terrigenous-carbonate rocks of the Hinggan series, the Paleozoic granitoid massives, the Cretaceous volcanic fields ; 3. Samples of the native gold

An appraisal of the hydrogeological processes involved in shallow subsurface radioactive waste management in Canadian terrain

International Nuclear Information System (INIS)

Grisak, G.E.; Jackson, R.E.

1978-01-01

The hydrogeological aspects of the problem of low-level radioactive waste management are introduced with a discussion of the Canadian nuclear power program; the nature of radioactive wastes and their rates of production; and the half-lives and health effects of ''waste'' radionuclides. As well, a general account is given of the present Canadian policy and procedures for licensing radioactive waste management sites. Following this introductory material, a detailed account is presented of the geohydrologic processes controlling the transport of radionuclides in groundwater flow systems and the attendant geochemical processes causing the retardation of the radionuclides. These geohydrologic and geochemical processes (i.e., hydrogeological processes) can be evaluated by the measurement of certain variables such as aquifer dispersivity, groundwater velocity, hydraulic conductivity, cation-exchange capacity, and total competing cations. To assess the possible importance of each variable in Canadian terrain, a comprehensive discussion of presently available (Canadian) data that have been compiled pertaining to each variable is presented. A description is then given of the hydrogeology of and the waste management experiences at radioactive waste management sites at Chalk River, Ontario; Bruce, Ontario; Whiteshell, Manitoba; and Suffield, Alberta. Along with this description there is a brief evaluation of those geohydrologic and geochemical processes that may be of importance at these sites. As a consequence of the above, site criteria outlining the nature of desirable hydrogeological environments for radioactive waste management areas are presented for those situations where the groundwater flow system acts as (a) a barrier to the migration of escaped radioactivity and (b) a joint dispersion-retardation system for liquid wastes. (author)

Geochemical consequences of the Chernobyl accident.; Geokhimicheskie posledstviya Chernobyl`skoj katastrofy.

Energy Technology Data Exchange (ETDEWEB)

Kopejkin, V A [VNIIGEOLNERUD, Kazan` (Russian Federation)

1994-12-31

Geochemical features of Cs, Sr, U, Pu behaviour in the zone of their hypergenesis are presented in the article. Necessary conditions for these elements filtration on the natural geochemical barriers are shown. Data of radionuclide composition of water for five years of observation in << Ryzhiy Les >> and dissolved forms of radionuclides are described. Geologic and hydrogeologic conditions of the Chernobyl NPP site are shortly characterized. Radionuclide composition in the ground water of contaminated water pools is analyzed. It is proposed to cover by the law all {alpha}-elements (Pu, Am, Np) and not only plutonium as it currently takes place.

PHREEQCI; a graphical user interface for the geochemical computer program PHREEQC

Science.gov (United States)

Charlton, Scott R.; Macklin, Clifford L.; Parkhurst, David L.

1997-01-01

PhreeqcI is a Windows-based graphical user interface for the geochemical computer program PHREEQC. PhreeqcI provides the capability to generate and edit input data files, run simulations, and view text files containing simulation results, all within the framework of a single interface. PHREEQC is a multipurpose geochemical program that can perform speciation, inverse, reaction-path, and 1D advective reaction-transport modeling. Interactive access to all of the capabilities of PHREEQC is available with PhreeqcI. The interface is written in Visual Basic and will run on personal computers under the Windows(3.1), Windows95, and WindowsNT operating systems.

Hydrologic-geochemical modeling needs for nuclear waste disposal systems performance assessments from the NEA perspective

International Nuclear Information System (INIS)

Muller, A.B.

1986-01-01

Credible scenarios for releases from high level nuclear waste repositories require radionuclides to be mobilized and transported by ground water. The capability to predict ground water flow velocities and directions as well as radionuclide concentrations in the flow system as a function of time are essential for assessing the performance of disposal systems. The first of these parameters can be estimated by hydrologic modeling while the concentrations can be predicted by geochemical modeling. The complementary use of empirical and phenomenological approaches to the geochemical modeling, when effectively coupled with hydrologic models can provide the tools needed for realistic performance assessment. An overview of the activities of the NEA in this area, with emphasis on the geochemical data bases (ISIRS for Ksub(d) data and the thermochemical data base critical review), rock/water interaction modeling (code development and short-courses), and hydrologic-geochemical code coupling (workshop and in-house activities) is presented in this paper from the perspective of probabilistic risk assessment needs. (author)

The EQ3/6 software package for geochemical modeling: Current status

International Nuclear Information System (INIS)

Worlery, T.J.; Jackson, K.J.; Bourcier, W.L.; Bruton, C.J.; Viani, B.E.; Knauss, K.G.; Delany, J.M.

1988-07-01

EQ3/6 is a software package for modeling chemical and mineralogic interactions in aqueous geochemical systems. The major components of the package are EQ3NR (a speciation-solubility code), EQ6 (a reaction path code), EQLIB (a supporting library), and a supporting thermodynamic data base. EQ3NR calculates aqueous speciation and saturation indices from analytical data. It can also be used to calculate compositions of buffer solutions for use in laboratory experiments. EQ6 computes reaction path models of both equilibrium step processes and kinetic reaction processes. These models can be computed for closed systems and relatively simple open systems. EQ3/6 is useful in making purely theoretical calculations, in designing, interpreting, and extrapolating laboratory experiments, and in testing and developing submodels and supporting data used in these codes. The thermodynamic data base supports calculations over the range 0-300 degree C. 60 refs., 2 figs

The EQ3/6 software package for geochemical modeling: Current status

Energy Technology Data Exchange (ETDEWEB)

Wolery, T.J.; Jackson, K.J.; Bourcier, W.L.; Bruton, C.J.; Viani, B.E.; Knauss, K.G.; Delany, J.M.

1988-07-01

EQ3/6 is a software package for modeling chemical and mineralogic interactions in aqueous geochemical systems. The major components of the package are EQ3NR (a speciation-solubility code), EQ6 (a reaction path code), EQLIB (a supporting library), and a supporting thermodynamic data base. EQ3NR calculates aqueous speciation and saturation indices from analytical data. It can also be used to calculate compositions of buffer solutions for use in laboratory experiments. EQ6 computes reaction path models of both equilibrium step processes and kinetic reaction processes. These models can be computed for closed systems and relatively simple open systems. EQ3/6 is useful in making purely theoretical calculations, in designing, interpreting, and extrapolating laboratory experiments, and in testing and developing submodels and supporting data used in these codes. The thermodynamic data base supports calculations over the range 0-300{degree}C. 60 refs., 2 figs.

[Geochemical characteristics of radon and mercury in soil gas in Lhasa, Tibet, China].

Science.gov (United States)

Zhou, Xiao-Cheng; Du, Jian-Guo; Wang, Chuan-Yuan; Cao, Zhong-Quan; Yi, Li; Liu, Lei

2007-03-01

The geochemical characteristics of radon and mercury in soil gas in Lhasa and vicinity are investigated based on the measurements of Rn and Hg concentrations, and environmental quality for Rn and Hg in soil gas was evaluated by means of the index of geoaccumulation. The data of Rn and Hg of 1 579 sampling site indicate that the values of environmental-geochemical background of Rn and Hg are 7 634.9 Bq/m3, 41.5 ng/m3 with standard deviations of 2.7 Bq/m3, 2.2 ng/m3, respectively. The environmental quality for Rn in soil gas is better in the west and east parts of studied area, but becomes moderate pollution (level III) in the north part of the central area. Rn is derived from radioactive elements in granitic sediments in the intermountain basin and granite base, which are the major sources of pollution. The environmental quality for Hg in soil gas becomes gradually polluted from the suburban to the center of urban, and the highest pollution reaches level IV. The background of Hg in soil gas is mainly controlled by compositions of sediments, but the Hg pollution caused by human waste and religionary use of mercury.

Microstructural Control on Perlite Expansibility and Geochemical Balance with a Novel Application of Isocon Analysis: An Example from Milos Island Perlite (Greece

Directory of Open Access Journals (Sweden)

Basilios Tsikouras

2016-08-01

Full Text Available Representative perlite bulk rock samples from two areas of Milos Island, Greece were collected and the expansion properties of their industrial product were investigated. Coarse crude perlite from Tsigrado exhibits better expansibility, which is assigned to the presence of coarser crystallites in its bulk parent rock. During thermal treatment, the finer crystallites of the coarse crude perlite from Trachilas are entrapped in the groundmass and lead to overheating, which inhibits expansion and eventually results in shrinkage. Geochemical modification of the expanded perlites relative to their crude precursors were investigated, using the isocon method. Volatilisation of crystalline water is the main factor controlling mass reduction of the expanded perlites. Other elements, during the adequate expansion of the Tsigrado perlite, can be classified into three categories. The elements that participate preferentially in crystals decrease in the expanded material at amounts higher than the total mass loss of the rock, due to their escape controlled mainly by the removal of the crystalline phases. The elements equally participating in crystals and the groundmass show losses equivalent to the total mass loss of the rocks, as they escaped in the crystalline phases and airborne particles from the groundmass during thermal treatment. Decrease of highly incompatible elements, which mostly participate in the groundmass, in the expanded products is less than the total mass loss, as they escaped mainly in the airborne particles. The inadequate expansion and burst of the Trachilas perlite did not allow for a similar categorisation, due to random and unpredictable escape of the elements. We propose the application of this method to an artificial system to predict unexpandable mineral phases in bulk perlite, as well as elements that are most likely to participate in the amorphous perlite phase, which cannot be determined from a regular industrial production line

Robust control charts in statistical process control

NARCIS (Netherlands)

Nazir, H.Z.

2014-01-01

The presence of outliers and contaminations in the output of the process highly affects the performance of the design structures of commonly used control charts and hence makes them of less practical use. One of the solutions to deal with this problem is to use control charts which are robust

Geochemical and Isotopic Interpretations of Groundwater Flow in the Oasis Valley Flow System, Southern Nevada

International Nuclear Information System (INIS)

Thomas, J.M.; Benedict, F.C. Jr.; Rose, T.P.; Hershey, R.L.; Paces, J.B.; Peterman, Z.E.; Farnham, I.M.; Johannesson, K.H.; Singh, A.K.; Stetzenbach, K.J.; Hudson, G.B.; Kenneally, J.M.; Eaton, G.F.; Smith, D.K.

2003-01-01

This report summarizes the findings of a geochemical investigation of the Pahute Mesa-Oasis Valley groundwater flow system in southwestern Nevada. It is intended to provide geochemical data and interpretations in support of flow and contaminant transport modeling for the Western and Central Pahute Mesa Corrective Action Units

Geochemical reactivity of rocks of the Czech Republic

Czech Academy of Sciences Publication Activity Database

Chuman, T.; Gürtlerová, P.; Hruška, Jakub; Adamová, M.

2014-01-01

Roč. 10, č. 2 (2014), s. 341-349 ISSN 1744-5647 R&D Projects: GA MŠk(CZ) ED1.1.00/02.0073 Institutional support: RVO:67179843 Keywords : geochemical reactivity * Czech Republic * susceptibility to weathering Subject RIV: EH - Ecology, Behaviour Impact factor: 1.193, year: 2014

Process recognition in multi-element soil and stream-sediment geochemical data

Science.gov (United States)

Grunsky, E.C.; Drew, L.J.; Sutphin, D.M.

2009-01-01

Stream-sediment and soil geochemical data from the Upper and Lower Coastal Plains of South Carolina (USA) were studied to determine relationships between soils and stream sediments. From multi-element associations, characteristic compositions were determined for both media. Primary associations of elements reflect mineralogy, including heavy minerals, carbonates and clays, and the effects of groundwater. The effects of groundwater on element concentrations are more evident in soils than stream sediments. A "winnowing index" was created using ratios of Th to Al that revealed differing erosional and depositional environments. Both soils and stream sediments from the Upper and Lower Coastal Plains show derivation from similar materials and subsequent similar multi-element relationships, but have some distinct differences. In the Lower Coastal Plain, soils have high values of elements concentrated in heavy minerals (Ce, Y, Th) that grade into high values of elements concentrated into finer-grain-size, lower-density materials, primarily comprised of carbonates and feldspar minerals (Mg, Ca, Na, K, Al). These gradational trends in mineralogy and geochemistry are inferred to reflect reworking of materials during marine transgressions and regressions. Upper Coastal Plain stream-sediment geochemistry shows a higher winnowing index relative to soil geochemistry. A comparison of the 4 media (Upper Coastal Plain soils and stream sediments and Lower Coastal Plain soils and stream sediments) shows that Upper Coastal Plain stream sediments have a higher winnowing index and a higher concentration of elements contained within heavy minerals, whereas Lower Coastal Plain stream sediments show a strong correlation between elements typically contained within clays. It is not possible to calculate a functional relationship between stream sediment-soil compositions for all elements due to the complex history of weathering, deposition, reworking and re-deposition. However, depending on

Geochemical evidence for seasonal controls on the transportation of Holocene loess, Matanuska Valley, southern Alaska, USA

Science.gov (United States)

Muhs, Daniel; Budahn, James R.; Skipp, Gary L.; McGeehin, John

2016-01-01

Loess is a widespread Quaternary deposit in Alaska and loess accretion occurs today in some regions, such as the Matanuska Valley. The source of loess in the Matanuska Valley has been debated for more than seven decades, with the Knik River and the Matanuska River, both to the east, being the leading candidates and the Susitna River, to the west, as a less favorable source. We report here new stratigraphic, mineralogic, and geochemical data that test the competing hypotheses of these river sources. Loess thickness data are consistent with previous studies that show that a source or sources lay to the east, which rules out the Susitna River as a source. Knik and Matanuska River silts can be distinguished using Sc–Th–La, LaN/YbN vs. Eu/Eu∗, Cr/Sc, and As/Sb. Matanuska Valley loess falls clearly within the range of values for these ratios found in Matanuska River silt. Dust storms from the Matanuska River are most common in autumn, when river discharge is at a minimum and silt-rich point bars are exposed, wind speed from the north is beginning to increase after a low-velocity period in summer, snow depth is still minimal, and soil temperatures are still above freezing. Thus, seasonal changes in climate and hydrology emerge as critical factors in the timing of aeolian silt transport in southern Alaska. These findings could be applicable to understanding seasonal controls on Pleistocene loess accretion in Europe, New Zealand, South America, and elsewhere in North America.

Geochemical maps of stream sediments in central Colorado, from New Mexico to Wyoming

Science.gov (United States)

Eppinger, Robert G.; Giles, Stuart A.; Klein, Terry L.

2015-01-01

The U.S. Geological Survey has completed a series of geologic, mineral resource, and environmental assessment studies in the Rocky Mountains of central Colorado, from Leadville eastward to the range front and from New Mexico to the Wyoming border. Regional stream-sediment geochemical maps, useful for assessing mineral resources and environmental effects of historical mining activities, were produced as part of the study. The data portrayed in this 56-parameter portfolio of landscape geochemical maps serve as a geochemical baseline for the region, indicate element abundances characteristic of various lithologic terranes, and identify gross anthropogenic effects of historical mining. However, although reanalyzed in this study by modern, sensitive methods, the majority of the stream-sediment samples were collected in the 1970s. Thus, metal concentrations portrayed in these maps represent stream-sediment geochemistry at the time of collection.

Patterns and variability in geochemical signatures and microbial activity within and between diverse cold seep habitats along the lower continental slope, Northern Gulf of Mexico

Science.gov (United States)

Bowles, Marshall; Hunter, Kimberley S.; Samarkin, Vladimir; Joye, Samantha

2016-07-01

We collected 69 sediment cores from distinct ecological and geological settings along the deep slope in the Northern Gulf of Mexico to evaluate whether specific geochemical- or habitat-related factors correlated with rates of microbial processes and geochemical signatures. By collecting replicate cores from distinct habitats across multiple sites, we illustrate and quantify the heterogeneity of cold seep geochemistry and microbial activity. These data also document the factors driving unique aspects of the geochemistry of deep slope gas, oil and brine seeps. Surprisingly little variation was observed between replicate (n=2-5) cores within sites for most analytes (except methane), implying that the common practice of collecting one core for geochemical analysis can capture the signature of a habitat in most cases. Depth-integrated concentrations of methane, dissolved inorganic carbon (DIC), and calcium were the predominant geochemical factors that correlated with a site's ecological or geological settings. Pore fluid methane concentration was related to the phosphate and DIC concentration, as well as to rates of sulfate reduction. While distinctions between seep habitats were identified from geochemical signatures, habitat specific geochemistry varied little across sites. The relative concentration of dissolved inorganic nitrogen versus phosphorus suggests that phosphorus availability limits biomass production at cold seeps. Correlations between calcium, chloride, and phosphate concentrations were indicative of brine-associated phosphate transport, suggesting that in addition to the co-migration of methane, dissolved organic carbon, and ammonium with brine, phosphate delivery is also associated with brine advection.

Geochemical modelling of the weathering zone of the 'Mina Fe' U deposit (Spain): A natural analogue for nuclear spent fuel alteration and stability processes in radwaste disposal

Energy Technology Data Exchange (ETDEWEB)

Arcos, D. [AMPHOS XXI Consulting S.L., Passeig de Rubi, 29-31, 08197 Valldoreix, Barcelona (Spain)], E-mail: david.arcos@amphos21.com; Perez del Villar, L. [CIEMAT, Dpto.de Medio Ambiente, Avda, Complutense 22, 28040 Madrid (Spain); Bruno, J.; Domenech, C. [AMPHOS XXI Consulting S.L., Passeig de Rubi, 29-31, 08197 Valldoreix, Barcelona (Spain)

2008-04-15

The 'Mina Fe' U deposit (Salamanca, Spain) has been studied in the context of Enresa's programme for U-mine sites restoration and also as a natural analogue for processes in high-level nuclear waste (HLNW) geological disposal. The investigations encompassed an array of geoscience disciplines, such as structural geology, mineralogy, hydrogeology and elemental and isotopic geochemistry and hydrogeochemistry of the site. Based on the obtained results, a conceptual mineralogical and geochemical model was performed integrating the main geochemical processes occurring at the site: the interaction between oxidised and slightly acidic water with pyrite, pitchblende, calcite and dolomite, as essential minerals of the U fracture-filling mineralisation, and hydroxyapatite from the host rock, as the main source of P. This conceptual model has been tested in a systematic numerical model, which includes the main kinetic (pyrite and pitchblende dissolution) and equilibrium processes (carbonate mineral dissolution, and goethite, schoepite and autunite secondary precipitation). The results obtained from the reactive-transport model satisfactorily agree with the conceptual model previously established. The assumption of the precipitation of coffinite as a secondary mineral in the system cannot be correctly evaluated due to the lack of hydrochemical data from the reducing zone of the site and valid thermodynamic and kinetic data for this hydrated U(IV)-silicate. This precipitation can also be hampered by the probable existence of dissolved U(IV)-organic matter and/or uranyl carbonate complexes, which are thermodynamically stable under the alkaline and reducing conditions that prevail in the reducing zone of the system. Finally, the intense downwards oxic and acidic alteration in the upper part of the system is of no relevance for the performance assessment of a HLNW disposal. However, the acidic and oxidised conditions are quickly buffered to neutral-alkaline and

Scaling Effects of Cr(VI) Reduction Kinetics. The Role of Geochemical Heterogeneity

Energy Technology Data Exchange (ETDEWEB)

Wang, Li [Pennsylvania State Univ., State College, PA (United States); Li, Li [Pennsylvania State Univ., State College, PA (United States)

2015-10-22

The natural subsurface is highly heterogeneous with minerals distributed in different spatial patterns. Fundamental understanding of how mineral spatial distribution patterns regulate sorption process is important for predicting the transport and fate of chemicals. Existing studies about the sorption was carried out in well-mixed batch reactors or uniformly packed columns, with few data available on the effects of spatial heterogeneities. As a result, there is a lack of data and understanding on how spatial heterogeneities control sorption processes. In this project, we aim to understand and develop modeling capabilities to predict the sorption of Cr(VI), an omnipresent contaminant in natural systems due to its natural occurrence and industrial utilization. We systematically examine the role of spatial patterns of illite, a common clay, in determining the extent of transport limitation and scaling effects associated with Cr(VI) sorption capacity and kinetics using column experiments and reactive transport modeling. Our results showed that the sorbed mass and rates can differ by an order of magnitude due to of the illite spatial heterogeneities and transport limitation. With constraints from data, we also developed the capabilities of modeling Cr(VI) in heterogeneous media. The developed model is then utilized to understand the general principles that govern the relationship between sorption and connectivity, a key measure of the spatial pattern characteristics. This correlation can be used to estimate Cr(VI) sorption characteristics in heterogeneous porous media. Insights gained here bridge gaps between laboratory and field application in hydrogeology and geochemical field, and advance predictive understanding of reactive transport processes in the natural heterogeneous subsurface. We believe that these findings will be of interest to a large number of environmental geochemists and engineers, hydrogeologists, and those interested in contaminant fate and transport

Geochemical indicators of gold ore fields

International Nuclear Information System (INIS)

Shcherbakov, Yu.G.

1995-01-01

The principles of selection of indicators for genetic reconstructions and prognostic valuations of gold mineralization of diverse morphological and geochemical types have been substantiated. The neutron-activation analysis with radiochemical separation and detection limit of 1-10 -8 %, instrumental neutron-activation analysis and atomic-absorption analysis are the main methods of determination of gold low contents in the rocks, as well as diverse elements, including transition, rare earth elements and tellurium, in gold. 50 refs.; 1 fig.; 3 tabs

GEOCHEMICAL AND ISOTOPIC CONSTRAINTS ON GROUND-WATER FLOW DIRECTIONS, MIXING AND RECHARGE AT YUCCA MOUNTAIN, NEVADA

International Nuclear Information System (INIS)

A. Meijer; E. Kwicklis

2000-01-01

conservative tracers such as chloride and/or groundwater age and unsaturated-zone thickness; (4) Correct 14 C ages for possible dilution of radiocarbon by calcite fracture coatings using geochemical reaction models; and (5) Establish mixing relations between waters from different source areas using relatively conservative species such as 2 H and 18 O or chloride and sulfate, and evaluate if inferred flow paths and mixing relations are reasonable based on chemical reactions required to reproduce the observed water chemistry. The analysis presented in this report is appropriate for the intended use described above. This analysis is not directly related to the principal factors, or other factors, for the post-closure safety case, nor is it used directly in calculations or analyses that provide estimates of the effects of potentially disruptive processes and events, as described in AP-3.15Q, Managing Technical Product Inputs

The aqueous solubility and speciation analysis for uranium, neptunium and selenium by the geochemical code(EQ3/6)

International Nuclear Information System (INIS)

Takeda, Seiji; Shima, Shigeki; Kimura, Hideo; Matsuzuru, Hideo

1995-11-01

The geochemical condition of a geologic disposal system of HLW controls the solubility and physicochemical forms of dominant aqueous species for elements, which are one of essential information required for safety assessment. Based on the measured compositions of groundwater, the compositions of groundwater in the disposal system were calculated. The solubility and speciation analyses for the polyvalent elements, uranium, neptunium, and selenium, were performed by the geochemical code EQ3/6. The results obtained were compared with the data appeared in the literatures on the solubilities and speciations. The geochemical behaviors of the elements with respect to the solubility and speciation could quantitatively be elucidated for the compositions of the interstitial waters in an engineered barrier and ground water in a natural barrier. In the pH range of neutral to alkali, the solubilities of U and Np tend to increase with an increase of the carbonate concentration in groundwater. This carbonate concentration dependence of the solubility was also estimated. In the engineered barrier the predominant aqueous species were specified, and in the natural barrier the change of aqueous species was also predicted while the chemical compositions changed from the reducing to oxidizing conditions. The dominant aqueous species for the elements, which migrate in and through the disposal system, were determined by the speciation analysis. (author)

Neural PID Control Strategy for Networked Process Control

Directory of Open Access Journals (Sweden)

Jianhua Zhang

2013-01-01

Full Text Available A new method with a two-layer hierarchy is presented based on a neural proportional-integral-derivative (PID iterative learning method over the communication network for the closed-loop automatic tuning of a PID controller. It can enhance the performance of the well-known simple PID feedback control loop in the local field when real networked process control applied to systems with uncertain factors, such as external disturbance or randomly delayed measurements. The proposed PID iterative learning method is implemented by backpropagation neural networks whose weights are updated via minimizing tracking error entropy of closed-loop systems. The convergence in the mean square sense is analysed for closed-loop networked control systems. To demonstrate the potential applications of the proposed strategies, a pressure-tank experiment is provided to show the usefulness and effectiveness of the proposed design method in network process control systems.

Lead transport in intra-oceanic subduction zones: 2D geochemical-thermo-mechanical modeling of isotopic signatures

NARCIS (Netherlands)

Baitsch-Ghirardello, B.; Stracke, A.; Connolly, J.A.D.; Nikolaeva, K.M.; Gerya, T.V.

2014-01-01

Understanding the physical-chemical mechanisms and pathways of geochemical transport in subduction zones remains a long-standing goal of subduction-related research. In this study, we perform fully coupled geochemical-thermo-mechanical (GcTM) numerical simulations to investigate Pb isotopic

Microbial iron cycling in acidic geothermal springs of Yellowstone National Park: Integrating molecular surveys, geochemical processes and isolation of novel Fe-active microorganisms

Directory of Open Access Journals (Sweden)

Mark A Kozubal

2012-03-01

Full Text Available Geochemical, molecular, and physiological analyses of microbial isolates were combined to study the geomicrobiology of acidic iron oxide mats in Yellowstone National Park (YNP. Nineteen sampling locations from 11 geothermal springs were studied ranging in temperature from 53 to 84 °C and pH 2.4 to 3.6. All iron-oxide mats exhibited high diversity of crenarchaeal sequences from the Sulfolobales, Thermoproteales, and Desulfurococcales. The predominant Sulfolobales sequences were highly similar to Metallosphaera yellowstonensis str. MK1, previously isolated from one of these sites. Other groups of archaea were consistently associated with different types of iron oxide mats, including undescribed members of the phyla Thaumarchaeota and Euryarchaeota. Bacterial sequences were dominated by relatives of Hydrogenobaculum spp. above 65-70 °C, but increased in diversity below 60 °C. Cultivation of relevant iron-oxidizing and iron-reducing microbial isolates included Sulfolobus str. MK3, Sulfobacillus str. MK2, Acidicaldus str. MK6, and a new candidate genus in the Sulfolobales referred to as Sulfolobales str. MK5. Strains MK3 and MK5 are capable of oxidizing ferrous iron autotrophically, while strain MK2 oxidizes iron mixotrophically. Similar rates of iron oxidation were observed for M. yellowstonensis str. MK1 and Sulfolobales str. MK5 cultures, and these rates are close to those measured in situ. Biomineralized phases of ferric iron varied among cultures and field sites, and included ferric oxyhydroxides, K-jarosite, goethite, hematite, and scorodite depending on geochemical conditions. Strains MK5 and MK6 are capable of reducing ferric iron under anaerobic conditions with complex carbon sources. The combination of geochemical and molecular data as well as physiological observations of isolates suggests that the community structure of acidic Fe mats is linked with Fe cycling across temperatures ranging from 53 to 88 oC.

Geochemical databases. Part 1. Pmatch: a program to manage thermochemical data. Part 2. The experimental validation of geochemical computer models

International Nuclear Information System (INIS)

Pearson, F.J. Jr.; Avis, J.D.; Nilsson, K.; Skytte Jensen, B.

1993-01-01

This work is carried out under cost-sharing contract with European Atomic Energy Community in the framework of its programme on Management and Storage of Radioactive Wastes. Part 1: PMATCH, A Program to Manage Thermochemical Data, describes the development and use of a computer program, by means of which new thermodynamic data from literature may be referenced to a common frame and thereby become internally consistent with an existing database. The report presents the relevant thermodynamic expressions and their use in the program is discussed. When there is not sufficient thermodynamic data available to describe a species behaviour under all conceivable conditions, the problems arising are thoroughly discussed and the available data is handled by approximating expressions. Part II: The Experimental Validation of Geochemical Computer models are the results of experimental investigations of the equilibria established in aqueous suspensions of mixtures of carbonate minerals (Calcium, magnesium, manganese and europium carbonates) compared with theoretical calculations made by means of the geochemical JENSEN program. The study revealed that the geochemical computer program worked well, and that its database was of sufficient validity. However, it was observed that experimental difficulties could hardly be avoided, when as here a gaseous component took part in the equilibria. Whereas the magnesium and calcium carbonates did not demonstrate mutual solid solubility, this produced abnormal effects when manganese and calcium carbonates were mixed resulting in a diminished solubility of both manganese and calcium. With tracer amounts of europium added to a suspension of calcite in sodium carbonate solutions long term experiments revealed a transition after 1-2 months, whereby the tracer became more strongly adsorbed onto calcite. The transition is interpreted as the nucleation and formation of a surface phase incorporating the 'species' NaEu(Co 3 ) 2

The relation between geochemical characteristics and landslide in Hungtsaiping area, Nantou, Taiwan

Science.gov (United States)

Lin, P.; Tsai, L.

2009-12-01

Hungtsaiping is located at the south bank of the Yonglu stream, Chungliao Village of Nantou County, central Taiwan. Hungtsaiping landslide was triggered by the Chi-Chi earthquake (Mw=7.6) occurring on September 20, 1999 UTC near the town of Chi-Chi in Nantou County, central Taiwan. Coping with the geological and geomorphologic investigations, this study makes an attempt to find the relation between geochemical characteristics and landslide in Hungtsaiping area. Water samples were collected from spring waters, creeks, ponds, groundwater and the Yonglu stream once every month from May 2008 to May 2009. Oxygen and hydrogen stable isotopic, ionic concentrations, as well as electrical conductivity and pH value were analyzed. The results indicate that calcium and magnesium bicarbonate-rich water was found on the top and the middle part of the slope. On the other hand, sodium bicarbonate-rich water as well as exceptionally high sulfate concentration was found on the foot of the slope, the sulfate content decreased with increasing elevations until the middle part of slope. A conceptual model of flow process and water origin in Hungtsaiping landslide was established by summarizing the features of hydrogeochemical analyses and the profiles in this study. Keywords: landslide, geochemical characteristics, isotope, hydrochemistry. Fig. 1 The sampling locations of Hungtsaiping landslide. Fig. 2 Isogram: the concentration of sulfate in May 2008 in Hungtsaiping area.

Similarity in Evolutionary Histories of Eocene Sediments from Subathu and Cambay Basins: Geochemical and Palaeontological Studies

Science.gov (United States)

Chaudhuri, S.; Halder, K.; Sarkar, S.

2017-12-01

A systematic comparative study of microfaunal assemblage and representative geochemical elements from two Cenozoic basins of India, Mangrol-Valia Lignite Mine section (21°30'52''N:73°12'20.5''E) of Cambay Shale Formation, western India and Jigni section (33°14'45"N:74°22'0"E) from Subathu Formation in northern India was undertaken to infer the paleoenvironment, palaeobathymetry and paleoclimate of these successions. Despite a gamut of work already carried out in these two basins, the sedimentary successions still await a correlative-detailed process-based facies, geochemical characterization and paleoenvironmental analysis. With a view to fulfill this gap, the present work was carried out by studying bulk rock XRD, XRF, clay mineralogy and analyzing calcareous microfossil foraminifera from samples at equivalent depth of these two basins which are situated thousands of kilometers apart and in different tectonic settings. The faunal assemblage of Eocene sediments of Mangrol-Valia section is indicative of shallow marine and inner shelf deposition with medium oxygen supply, while that of the Jigni section suggests primarily a shallow marine condition, which gradually changes to open marine condition with time. It is pertinent to note that the two basins of Cenozoic India started their lithosuccession with coal bearing strata. Well preserved pectin aragonite shells also indicate that primarily these two basins experienced low energy lagoonal environment. The fossil assemblage in both basins also suggests a tropical moist to terrestrial lowland environment. Geochemical analysis shows that the Mangrol-Valia section mineralogically comprises of kaolinite, siderite, quartz, smectite and kaolinite with higher abundance throughout the succession indicating chemical weathering of Deccan basement and high erosional environment. Calcite is the main constituent of Jigni section that indicates intracratonic rift settings. Medium to high quartz content and other detrital

Research on geochemical exploration in geotherm development

International Nuclear Information System (INIS)

Hirowatari, Kazuo; Imaizumi, Yukio; Koga, Akito; Iwanaga, Tatsuto.

1987-01-01

The decisive factor of geotherm development is to improve the exploration techniques. By effectively carrying out the selection of promising development spots and the decision of well drilling positions, the geotherm development exceeding existing energy sources becomes feasible. There have been many problems in conventional geotherm exploration such as the high cost and long work period, therefore, it was decided to advance the research on geochemical exploration techniques which are relatively simple and can be carried out with low cost. When the techniques of geochemistry are used, for example, in the case that there are hot springs or fumaroles, the temperature, origin, properties and so on of underground hot water reservoirs can be estimated from their chemical composition. The method of examining the mercury concentration in soil and soil air has been in practical use in the geothermal districts where the ground surface symptom lacks. This time, the method of investigation using radon, thoron and gamma ray as the exploration indices was newly studied. The index compositions for geochemical exploration, new exploration index compositions, the method of measurement, the basic investigation and on-the-spot investigation are reported. (Kako, I.)

Mineralogical, micromorphological and geochemical transformations in the initial steps of the weathering process of charnockite from the Caparaó Range, southeastern Brazil

Science.gov (United States)

Soares, Caroline Cibele Vieira; Varajão, Angélica Fortes Drummond Chicarino; Varajão, César Augusto Chicarino; Boulangé, Bruno

2014-12-01

X-ray diffraction (XRD), X-ray Fluorescence (XRF), optical microscopy, Scanning Electron Microscopy coupled with Energy Dispersive Spectrometry (SEM-EDS) and Electron Probe micro-analyser (EPMA) and Wavelength-Dispersive Spectroscopy (WDS) were conducted on charnockite from the Caparaó Suite and its alteration cortex to determine the mineralogical, micromorphological and geochemical transformations resulting from the weathering process. The hydrolysis of the charnockite occurred in different stages, in accordance with the order of stability of the minerals with respect to weathering: andesine/orthopyroxene, pargasite and alkali feldspar. The rock modifications had begun with the formation of a layer of incipient alteration due to the percolation of weathering solutions first in the pressure relief fractures and then in cleavage and mineral edges. The iron exuded from ferromagnesian minerals precipitated in the intermineral and intramineral discontinuities. The layer of incipient alteration evolves into an inner cortex where the plagioclase changes into gibbsite by direct alitisation, the ferromagnesian minerals initiate the formation of goethitic boxworks with kaolinitic cores, and the alkali feldspar initiates indirect transformation into gibbsite, forming an intermediate phase of illite and kaolinite. In the outer cortex, mostly traces of alkali feldspar remain, and they are surrounded by goethite and gibbsite as alteromorphics, characterising the formation of the isalteritic horizon that occurs along the slope and explains the bauxitization process at the Caparaó Range, SE Brazil.

A >100 Ma Mantle Geochemical Record: Retiring Mantle Plumes may be Premature

Science.gov (United States)

Konter, J. G.; Hanan, B. B.; Blichert-Toft, J.; Koppers, A. A.; Plank, T.; Staudigel, H.

2006-12-01

Hotspot volcanism has long been attributed to mantle plumes, but in recent years suggestions have been made that plate tectonic processes, such as extension, can account for all hotspot tracks. This explanation involves a profoundly less dynamic lower mantle, which justifies a critical evaluation before the plume model is dismissed. Such an evaluation has to involve a wide range of geochemical, geological, and geophysical techniques, broadly investigating the products of volcanism as well as the underlying lithosphere and mantle. We argue here that the combined geological record and geochemistry of intraplate volcanoes holds some important clues that help us decide between models of plume-like upwelling versus passive upwelling with lithospheric extension. The best of these integrated datasets can be obtained from the long seamount chains in the Pacific Ocean. A new combined dataset of trace element and isotopic compositions, along with modern 40Ar/39Ar ages from seamounts in the Gilbert Ridge, Tokelau chain, and West Pacific Seamount Province (WPSP) provides a record of current to Cretaceous volcanism in the South Pacific. We have reconstructed the eruptive locations of the seamounts using a range of absolute plate motion models, including some models with hotspot motion and others that use the Indo-Atlantic hotspot reference frame. Our results show that the backtracked locations consistently form clusters (300km radius) around the active ends of the Macdonald, Rurutu and Rarotonga hotspot chains, while closely matching their distinct C-HIMU and C-EM1 signatures. The oldest WPSP seamounts (older than 100 Ma) form the only exception and backtrack, with larger uncertainty, to north of Rarotonga. Therefore, the mantle currently underlying the Cook-Austral islands has produced volcanoes in three geochemically distinct areas for at least 100 m.y. Furthermore, we find the shortest mantle residence time, 0.6 Ga, for a source of mixed recycled DMM and an EM1-like

A NEW BENCHMARK FOR PLANTWIDE PROCESS CONTROL

Directory of Open Access Journals (Sweden)

N. Klafke

Full Text Available Abstract The hydrodealkylation process of toluene (HDA has been used as a case study in a large number of control studies. However, in terms of industrial application, this process has become obsolete and is nowadays superseded by new technologies capable of processing heavy aromatic compounds, which increase the added value of the raw materials, such as the process of transalkylation and disproportionation of toluene (TADP. TADP also presents more complex feed and product streams and challenging operational characteristics both in the reactor and separator sections than in HDA. This work is aimed at proposing the TADP process as a new benchmark for plantwide control studies in lieu of the HAD process. For this purpose, a nonlinear dynamic rigorous model for the TADP process was developed using Aspen Plus™ and Aspen Dynamics™ and industrial conditions. Plantwide control structures (oriented to control and to the process were adapted and applied for the first time for this process. The results show that, even though both strategies are similar in terms of control performance, the optimization of economic factors must still be sought.

Geochemical processes and compacted bentonite FEBEX with a thermohydraulic gradient with a thermohydraulic gradient

International Nuclear Information System (INIS)

Leguey Jimenez, S.; Cuevas Rodriguez, J.; Martin Barca, M.; Vigil de la Villa Mencia, R.; Ramirez Martin, S.; Garcia Gimenez, R.

2002-01-01

At present, the main source of High Level radioactive Waste (HLW) is the electrical energy production during all sep of developing. In almost all the countries with nuclear programs, the option for the final management of HLW is the Deep Geological Repository (DGR), based on the concept of multi barrier. According to this concept, the wastes is isolated from biosphere by the interposition of confinement barrier. In the context of an investigation of the near field for a repository of HLW, the FEBEX Project, a set of laboratory test has been designed to give a better understanding of the thermo-hydro-mechanical and geochemical behaviour of the compacted bentonite as a confinement barrier. The object of these work is to analyse the properties of the bentonite and its behaviour under conditions that will be found in a repository. The precipitation of mineral phases, due to local changes in the chemical equilibrium and the hydration itself, can produce changes in the salinity of the interstitial water and in the microstructural organisation of the clay particles. the hydraulic and mechanical properties of the bentonite can be modified by the special conditions of the barrier. (Author)

Geochemical studies of potential source minerals of radon: case studies in Hungary

Energy Technology Data Exchange (ETDEWEB)

Rajnai, G.; Nagy-Balogh, J.; Gal-Solymos, K.; Konc, Z.; Breitner, D.; Barabas, A.; Szabo, C. [Eotvos Univ., Lithosphere Fluid Research Lab, Dept. of Petrology and Geochemistry, Budapest (Hungary); Barabas, A. [Eotvos Univ., Dept. of Geophysics, Budapest (Hungary)

2006-07-01

In Hungary, during the past decade five distinct regions have been chosen to find possible explanations of the uncommonly high radon background radiation values. The main aim of the research is to study U- and Th-bearing minerals in petrographic and geochemical characters. Besides the microscopic techniques, whole rock and in situ geochemical analytical methods were applied to determine the bulk U and Th content of the studied geological samples. We assume that some of the radon measured is related to the U and Th contents of the samples. (authors)

Geochemical evolution of the near field of a KBS-3 repository

International Nuclear Information System (INIS)

Arcos, David; Grandia, Fidel; Domenech, Cristina

2006-09-01

The Swedish concept developed by SKB for deep radioactive waste disposal, envisages an engineered multi-barrier system surrounding the nuclear waste (near field). In the present study we developed a numerical model to assess the geochemical evolution of the near field in the frame of the SKB's safety assessment SR-Can. These numerical models allow us to predict the long-term geochemical evolution of the near field system by means of reactive-transport codes and the information gathered in underground laboratory experiments and natural analogues. Two different scenarios have been defined to model this near field evolution, according to the pathway used by groundwater to contact the near field: a) through a fracture in the host rock intersecting the deposition hole; and b) through the material used to backfill the deposition tunnel. Moreover, we also modelled the effect of different groundwater compositions reaching the near field, as the up-rise of deep-seated brines and the intrusion of ice-melting derived groundwater. We also modelled the effect of the thermal stage due to the heat generated by spent fuel on the geochemical evolution of the bentonite barrier

Geochemical properties and nuclear chemical characteristics of Oklo natural fission reactors

Energy Technology Data Exchange (ETDEWEB)

Hidaka, Hiroshi [Hiroshima Univ., Higashi-Hiroshima (Japan). Faculty of Science

1997-07-01

There are six uranium deposits in the Gabonese Republic in the cnetral Africa. `Fission reactor zone`, the fission chain reactions generated about 200 billion years ago, was existed in a part of them. CEA begun geochemical researches of Oklo deposits etc. in 1991. The geochemical and nuclear chemical properties of Oklo were reviewed from the results of researches. Oklo deposits is consisted of main five sedimentary faces such as sandstone (FA), Black Shale formation (FB), mudstone (FC), tuff (FD) and volcaniclastic sandstone (FE) from the bottom on the base rock of granite in the Precambrian era. Uranium is enriched in the upper part of FA layer and the under part of FB layer. {sup 235}U/{sup 238}U, U content, fission proportion, duration time, neutron fluence, temperature, restitution factor of {sup 235}U and epithermal index ({gamma}) were investigated and compared. The geochemical properties of Oklo are as followed: large enrich of uranium, the abundance ratio of {sup 235}U as same as that of enriched uranium, interaction of natural water and small rear earth elements. These factors made casually Oklo fission reactor. (S.Y.)

Geochemical evolution of the near field of a KBS-3 repository

Energy Technology Data Exchange (ETDEWEB)

Arcos, David; Grandia, Fidel; Domenech, Cristina [Enviros Spain S.L., Barcelona (Spain)

2006-09-15

The Swedish concept developed by SKB for deep radioactive waste disposal, envisages an engineered multi-barrier system surrounding the nuclear waste (near field). In the present study we developed a numerical model to assess the geochemical evolution of the near field in the frame of the SKB's safety assessment SR-Can. These numerical models allow us to predict the long-term geochemical evolution of the near field system by means of reactive-transport codes and the information gathered in underground laboratory experiments and natural analogues. Two different scenarios have been defined to model this near field evolution, according to the pathway used by groundwater to contact the near field: a) through a fracture in the host rock intersecting the deposition hole; and b) through the material used to backfill the deposition tunnel. Moreover, we also modelled the effect of different groundwater compositions reaching the near field, as the up-rise of deep-seated brines and the intrusion of ice-melting derived groundwater. We also modelled the effect of the thermal stage due to the heat generated by spent fuel on the geochemical evolution of the bentonite barrier.

Establishing nursery estuary otolith geochemical tags for Sea Bass (Dicentrarchus labrax): Is temporal stability estuary dependent?

Science.gov (United States)

Ryan, Diarmuid; Wögerbauer, Ciara; Roche, William

2016-12-01

The ability to determine connectivity between juveniles in nursery estuaries and adult populations is an important tool for fisheries management. Otoliths of juvenile fish contain geochemical tags, which reflect the variation in estuarine elemental chemistry, and allow discrimination of their natal and/or nursery estuaries. These tags can be used to investigate connectivity patterns between juveniles and adults. However, inter-annual variability of geochemical tags may limit the accuracy of nursery origin determinations. Otolith elemental composition was used to assign a single cohort of 0-group sea bass Dicentrarchus labrax to their nursery estuary thus establishing an initial baseline for stocks in waters around Ireland. Using a standard LDFA model, high classification accuracies to nursery sites (80-88%) were obtained. Temporal stability of otolith geochemical tags was also investigated to assess if annual sampling is required for connectivity studies. Geochemical tag stability was found to be strongly estuary dependent.

A preliminary report of geochemical investigations in the Blackbird District

Science.gov (United States)

Canney, F.C.; Hawkes, H.E.; Richmond, G.M.; Vhay, J. S.

1953-01-01

This paper reviews an experimental geochemical prospecting survey in the Blackbird cobalt-copper mining district. The district is in east-central Idaho, about 20 miles west-southwest of Salmon. The area is one of deeply weathered nearly flat-topped upland surfaces cut by steep-walled valleys which are tributary to the canyon of Panther Creek. Most of the area has a relatively heavy vegetative cover, and outcrops are scarce except on the sides of the steeper valleys* Because of the importance of the surficial deposits and soils and the physiographic history of the region on the interpretation of the geochemical data, a separate chapter on this subject by Gerald H. Richmond follows the following brief description of the geology of the district.

Closed-Loop Process Control for Electron Beam Freeform Fabrication and Deposition Processes

Science.gov (United States)

Taminger, Karen M. (Inventor); Hafley, Robert A. (Inventor); Martin, Richard E. (Inventor); Hofmeister, William H. (Inventor)

2013-01-01

A closed-loop control method for an electron beam freeform fabrication (EBF(sup 3)) process includes detecting a feature of interest during the process using a sensor(s), continuously evaluating the feature of interest to determine, in real time, a change occurring therein, and automatically modifying control parameters to control the EBF(sup 3) process. An apparatus provides closed-loop control method of the process, and includes an electron gun for generating an electron beam, a wire feeder for feeding a wire toward a substrate, wherein the wire is melted and progressively deposited in layers onto the substrate, a sensor(s), and a host machine. The sensor(s) measure the feature of interest during the process, and the host machine continuously evaluates the feature of interest to determine, in real time, a change occurring therein. The host machine automatically modifies control parameters to the EBF(sup 3) apparatus to control the EBF(sup 3) process in a closed-loop manner.

Markov processes and controlled Markov chains

CERN Document Server

Filar, Jerzy; Chen, Anyue

2002-01-01

The general theory of stochastic processes and the more specialized theory of Markov processes evolved enormously in the second half of the last century. In parallel, the theory of controlled Markov chains (or Markov decision processes) was being pioneered by control engineers and operations researchers. Researchers in Markov processes and controlled Markov chains have been, for a long time, aware of the synergies between these two subject areas. However, this may be the first volume dedicated to highlighting these synergies and, almost certainly, it is the first volume that emphasizes the contributions of the vibrant and growing Chinese school of probability. The chapters that appear in this book reflect both the maturity and the vitality of modern day Markov processes and controlled Markov chains. They also will provide an opportunity to trace the connections that have emerged between the work done by members of the Chinese school of probability and the work done by the European, US, Central and South Ameri...

Overview of the geochemical code MINTEQ: applications to performance assessment for low-level wastes

International Nuclear Information System (INIS)

Graham, M.J.; Peterson, S.R.

1985-09-01

The MINTEQ geochemical computer code, developed at Pacific Northwest Laboratory, integrates many of the capabilities of its two immediate predecessors, WATEQ3 and MINEQL. MINTEQ can be used to perform the calculations necessary to simulate (model) the contact of low-level waste solutions with heterogeneous sediments or the interaction of ground water with solidified low-level wastes. The code is capable of performing calculations of ion speciation/solubility, adsorption, oxidation-reduction, gas phase equilibria, and precipitation/dissolution of solid phases. Under the Special Waste Form Lysimeters-Arid program, the composition of effluents (leachates) from column and batch experiments, using laboratory-scale waste forms, will be used to develop a geochemical model of the interaction of ground water with commercial solidified low-level wastes. The wastes being evaluated include power reactor waste streams that have been solidified in cement, vinyl ester-styrene, and bitumen. The thermodynamic database for the code is being upgraded before the geochemical modeling is performed. Thermodynamic data for cobalt, antimony, cerium, and cesium solid phases and aqueous species are being added to the database. The need to add these data was identified from the characterization of the waste streams. The geochemical model developed from the laboratory data will then be applied to predict the release from a field-lysimeter facility that contains full-scale waste samples. The contaminant concentrations migrating from the wastes predicted using MINTEQ will be compared to the long-term lysimeter data. This comparison will constitute a partical field validation of the geochemical model. 28 refs

Fundamentals of semiconductor manufacturing and process control

CERN Document Server

May, Gary S

2006-01-01

A practical guide to semiconductor manufacturing from process control to yield modeling and experimental design Fundamentals of Semiconductor Manufacturing and Process Control covers all issues involved in manufacturing microelectronic devices and circuits, including fabrication sequences, process control, experimental design, process modeling, yield modeling, and CIM/CAM systems. Readers are introduced to both the theory and practice of all basic manufacturing concepts. Following an overview of manufacturing and technology, the text explores process monitoring methods, including those that focus on product wafers and those that focus on the equipment used to produce wafers. Next, the text sets forth some fundamentals of statistics and yield modeling, which set the foundation for a detailed discussion of how statistical process control is used to analyze quality and improve yields. The discussion of statistical experimental design offers readers a powerful approach for systematically varying controllable p...

Geochemical characteristics of oil sands fluid petroleum coke

International Nuclear Information System (INIS)

Nesbitt, Jake A.; Lindsay, Matthew B.J.; Chen, Ning

2017-01-01

The geochemical characteristics of fluid petroleum coke from the Athabasca Oil Sands Region (AOSR) of northern Alberta, Canada were investigated. Continuous core samples were collected to 8 m below surface at several locations (n = 12) from three coke deposits at an active oil sands mine. Bulk elemental analyses revealed the coke composition was dominated by C (84.2 ± 2.3 wt%) and S (6.99 ± 0.26 wt%). Silicon (9210 ± 3000 mg kg"−"1), Al (5980 ± 1200 mg kg"−"1), Fe (4760 ± 1200 mg kg"−"1), and Ti (1380 ± 430 mg kg"−"1) were present in lesser amounts. Vanadium (1280 ± 120 mg kg"−"1) and Ni (230 ± 80 mg kg"−"1) exhibited the highest concentrations among potentially-hazardous minor and trace elements. Sequential extractions revealed potential for release of these metals under field-relevant conditions. Synchrotron powder X-ray diffraction revealed the presence of Si and Ti oxides, organically-complexed V and hydrated Ni sulfate, and provided information about the asphaltenic carbon matrix. X-ray absorption near edge structure (XANES) spectroscopy at the V and Ni K-edges revealed that these metals were largely hosted in porphyrins and similar organic complexes throughout coke grains. Minor differences among measured V and Ni K-edge spectra were largely attributed to slight variations in local coordination of V(IV) and Ni(II) within these organic compounds. However, linear combination fits were improved by including reference spectra for inorganic phases with octahedrally-coordinated V(III) and Ni(II). Sulfur and Fe K-edge XANES confirmed that thiophenic coordination and pyritic-ilmenitic coordination are predominant, respectively. These results provide new information on the geochemical and mineralogical composition of oil sands fluid petroleum coke and improve understanding of potential controls on associated water chemistry. - Highlights: • Oil sands fluid petroleum coke contains wide range of major, minor and

Control System Design for Cylindrical Tank Process Using Neural Model Predictive Control Technique

Directory of Open Access Journals (Sweden)

M. Sridevi

2010-10-01

Full Text Available Chemical manufacturing and process industry requires innovative technologies for process identification. This paper deals with model identification and control of cylindrical process. Model identification of the process was done using ARMAX technique. A neural model predictive controller was designed for the identified model. The performance of the controllers was evaluated using MATLAB software. The performance of NMPC controller was compared with Smith Predictor controller and IMC controller based on rise time, settling time, overshoot and ISE and it was found that the NMPC controller is better suited for this process.

A survey of process control computers at the Idaho Chemical Processing Plant

International Nuclear Information System (INIS)

Dahl, C.A.

1989-01-01

The Idaho Chemical Processing Plant (ICPP) at the Idaho National Engineering Laboratory is charged with the safe processing of spent nuclear fuel elements for the United States Department of Energy. The ICPP was originally constructed in the late 1950s and used state-of-the-art technology for process control at that time. The state of process control instrumentation at the ICPP has steadily improved to keep pace with emerging technology. Today, the ICPP is a college of emerging computer technology in process control with some systems as simple as standalone measurement computers while others are state-of-the-art distributed control systems controlling the operations in an entire facility within the plant. The ICPP has made maximal use of process computer technology aimed at increasing surety, safety, and efficiency of the process operations. Many benefits have been derived from the use of the computers for minimal costs, including decreased misoperations in the facility, and more benefits are expected in the future

PhreeqcRM: A reaction module for transport simulators based on the geochemical model PHREEQC

Science.gov (United States)

Parkhurst, David L.; Wissmeier, Laurin

2015-01-01

PhreeqcRM is a geochemical reaction module designed specifically to perform equilibrium and kinetic reaction calculations for reactive transport simulators that use an operator-splitting approach. The basic function of the reaction module is to take component concentrations from the model cells of the transport simulator, run geochemical reactions, and return updated component concentrations to the transport simulator. If multicomponent diffusion is modeled (e.g., Nernst–Planck equation), then aqueous species concentrations can be used instead of component concentrations. The reaction capabilities are a complete implementation of the reaction capabilities of PHREEQC. In each cell, the reaction module maintains the composition of all of the reactants, which may include minerals, exchangers, surface complexers, gas phases, solid solutions, and user-defined kinetic reactants.PhreeqcRM assigns initial and boundary conditions for model cells based on standard PHREEQC input definitions (files or strings) of chemical compositions of solutions and reactants. Additional PhreeqcRM capabilities include methods to eliminate reaction calculations for inactive parts of a model domain, transfer concentrations and other model properties, and retrieve selected results. The module demonstrates good scalability for parallel processing by using multiprocessing with MPI (message passing interface) on distributed memory systems, and limited scalability using multithreading with OpenMP on shared memory systems. PhreeqcRM is written in C++, but interfaces allow methods to be called from C or Fortran. By using the PhreeqcRM reaction module, an existing multicomponent transport simulator can be extended to simulate a wide range of geochemical reactions. Results of the implementation of PhreeqcRM as the reaction engine for transport simulators PHAST and FEFLOW are shown by using an analytical solution and the reactive transport benchmark of MoMaS.

Modules based on the geochemical model PHREEQC for use in scripting and programming languages

Science.gov (United States)

Charlton, Scott R.; Parkhurst, David L.

2011-01-01

The geochemical model PHREEQC is capable of simulating a wide range of equilibrium reactions between water and minerals, ion exchangers, surface complexes, solid solutions, and gases. It also has a general kinetic formulation that allows modeling of nonequilibrium mineral dissolution and precipitation, microbial reactions, decomposition of organic compounds, and other kinetic reactions. To facilitate use of these reaction capabilities in scripting languages and other models, PHREEQC has been implemented in modules that easily interface with other software. A Microsoft COM (component object model) has been implemented, which allows PHREEQC to be used by any software that can interface with a COM server—for example, Excel®, Visual Basic®, Python, or MATLAB". PHREEQC has been converted to a C++ class, which can be included in programs written in C++. The class also has been compiled in libraries for Linux and Windows that allow PHREEQC to be called from C++, C, and Fortran. A limited set of methods implements the full reaction capabilities of PHREEQC for each module. Input methods use strings or files to define reaction calculations in exactly the same formats used by PHREEQC. Output methods provide a table of user-selected model results, such as concentrations, activities, saturation indices, and densities. The PHREEQC module can add geochemical reaction capabilities to surface-water, groundwater, and watershed transport models. It is possible to store and manipulate solution compositions and reaction information for many cells within the module. In addition, the object-oriented nature of the PHREEQC modules simplifies implementation of parallel processing for reactive-transport models. The PHREEQC COM module may be used in scripting languages to fit parameters; to plot PHREEQC results for field, laboratory, or theoretical investigations; or to develop new models that include simple or complex geochemical calculations.

Temporal dynamics of biogeochemical processes at the Norman Landfill site

Science.gov (United States)

Arora, Bhavna; Mohanty, Binayak P.; McGuire, Jennifer T.; Cozzarelli, Isabelle M.

2013-01-01

The temporal variability observed in redox sensitive species in groundwater can be attributed to coupled hydrological, geochemical, and microbial processes. These controlling processes are typically nonstationary, and distributed across various time scales. Therefore, the purpose of this study is to investigate biogeochemical data sets from a municipal landfill site to identify the dominant modes of variation and determine the physical controls that become significant at different time scales. Data on hydraulic head, specific conductance, δ2H, chloride, sulfate, nitrate, and nonvolatile dissolved organic carbon were collected between 1998 and 2000 at three wells at the Norman Landfill site in Norman, OK. Wavelet analysis on this geochemical data set indicates that variations in concentrations of reactive and conservative solutes are strongly coupled to hydrologic variability (water table elevation and precipitation) at 8 month scales, and to individual eco-hydrogeologic framework (such as seasonality of vegetation, surface-groundwater dynamics) at 16 month scales. Apart from hydrologic variations, temporal variability in sulfate concentrations can be associated with different sources (FeS cycling, recharge events) and sinks (uptake by vegetation) depending on the well location and proximity to the leachate plume. Results suggest that nitrate concentrations show multiscale behavior across temporal scales for different well locations, and dominant variability in dissolved organic carbon for a closed municipal landfill can be larger than 2 years due to its decomposition and changing content. A conceptual framework that explains the variability in chemical concentrations at different time scales as a function of hydrologic processes, site-specific interactions, and/or coupled biogeochemical effects is also presented.

Control of Pressure Process Using Infineon Microcontroller

Directory of Open Access Journals (Sweden)

A. Siddique

2007-07-01

Full Text Available The main objective of this paper is to design a cost effective controller for real time implementation of pressure process using Infineon micro controller (SAB 80C517A. Model Identification is performed and it is found to be First Order Plus Dead Time Process (FOPDT. The performance measure is tabulated for different parameter and it is found that Proportional (P controller is suitable for controlling the process.

Characterization of the geochemical processes present in the radionuclides and metals mobilization in the tailing dam at the Uranium Mining and Milling Facilities - Pocos de Caldas, MG, Brazil

International Nuclear Information System (INIS)

Pinto, Patricia Freitas

1995-08-01

In Brazil, the first step of nuclear fuel cycle - the mining and milling of the uranium ore - is developed at the Uranium Mining and Milling Facilities of Pocos de Caldas, Minas Gerais state. The wastes management is a very important aspect of the process. The understanding of the geochemical processes that occur in the tailings dam is a key question to define a plan of action concerning the decommissioning strategy of the facility. The objective of the present work was to give some issues to help in the adoption of the remedial actions concerning the decommissioning of the facility. It focused on the characterization of the most important geochemical processes regulating the mobilization of radionuclides and heavy metals in the tailings dam. Two cores from the tailings dam (uncovered area) were collected. Seepage and drainage waters were sampled, the same being true for the tailings dam lake. Groundwater form an aquifer bellow the tailings dam and superficial waters from a river that receives the effluents of the dam (Soberbo River) were also sampled. Data from the mining company were used to calculate the inventory of radionuclides and heavy metals deposited in the waste dam.The obtained results showed that pyrite oxidation is the key process in the mobilization of radionuclides and heavy metals from the wastes. Pyrite oxidation is a process regulated by oxygen diffusion and water. In the studied scenario it could be shown that the process was limited to a one meter deep layer in the uncovered part of the waste dam. Because of this, Fe, Al, Mn, Zn, Th and 238 U showed higher concentrations in the bottom layers of the cores in relation to the upper ones. 226 Ra and 210 Pb showed opposite patterns. The coprecipitation with Ca SO 4 was the most relevant mechanism in both radionuclides immobilization in the wastes. Sulfate was the only chemical species that could be assigned as a contaminant in aquifer bellow the waste dam. As a conclusion, the target environmental

Mining inventory of Uruguay. Polanco fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H; Artignan, D; Vairon, P

1982-01-01

This work is about the geochemical prospecting carried out in Polanco fotoplano within the framework of Uruguay Mining inventory . In this work were covered 660 km2 obtaining 685 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

Mineral and Geochemical Classification From Spectroscopy/Diffraction Through Neural Networks

Science.gov (United States)

Ferralis, N.; Grossman, J.; Summons, R. E.

2017-12-01

Spectroscopy and diffraction techniques are essential for understanding structural, chemical and functional properties of geological materials for Earth and Planetary Sciences. Beyond data collection, quantitative insight relies on experimentally assembled, or computationally derived spectra. Inference on the geochemical or geophysical properties (such as crystallographic order, chemical functionality, elemental composition, etc.) of a particular geological material (mineral, organic matter, etc.) is based on fitting unknown spectra and comparing the fit with consolidated databases. The complexity of fitting highly convoluted spectra, often limits the ability to infer geochemical characteristics, and limits the throughput for extensive datasets. With the emergence of heuristic approaches to pattern recognitions though machine learning, in this work we investigate the possibility and potential of using supervised neural networks trained on available public spectroscopic database to directly infer geochemical parameters from unknown spectra. Using Raman, infrared spectroscopy and powder x-ray diffraction from the publicly available RRUFF database, we train neural network models to classify mineral and organic compounds (pure or mixtures) based on crystallographic structure from diffraction, chemical functionality, elemental composition and bonding from spectroscopy. As expected, the accuracy of the inference is strongly dependent on the quality and extent of the training data. We will identify a series of requirements and guidelines for the training dataset needed to achieve consistent high accuracy inference, along with methods to compensate for limited of data.

Biogeochemical Processes Controlling Microbial Reductive Precipitation of Radionuclides

International Nuclear Information System (INIS)

Fredrickson, James K.; Brooks, Scott C.

2004-01-01

This project is focused on elucidating the principal biogeochemical reactions that govern the concentrations, chemical speciation, and distribution of the redox sensitive contaminants uranium (U) and technetium (Tc) between the aqueous and solid phases. The research is designed to provide new insights into the under-explored areas of competing geochemical and microbiological oxidation-reduction reactions that govern the fate and transport of redox sensitive contaminants and to generate fundamental scientific understanding of the identity and stoichiometry of competing microbial reduction and geochemical oxidation reactions. These goals and objectives are met through a series of hypothesis-driven tasks that focus on (1) the use of well-characterized microorganisms and synthetic and natural mineral oxidants, (2) advanced spectroscopic and microscopic techniques to monitor redox transformations of U and Tc, and (3) the use of flow-through experiments to more closely approximate groundwater environments. The results are providing an improved understanding and predictive capability of the mechanisms that govern the redox dynamics of radionuclides in subsurface environments. For purposes of this poster, the results are divided into three sections: (1) influence of Ca on U(VI) bioreduction; (2) localization of biogenic UO 2 and TcO 2 ; and (3) reactivity of Mn(III/IV) oxides.

Low Activity Waste Feed Process Control Strategy

International Nuclear Information System (INIS)

STAEHR, T.W.

2000-01-01

The primary purpose of this document is to describe the overall process control strategy for monitoring and controlling the functions associated with the Phase 1B high-level waste feed delivery. This document provides the basis for process monitoring and control functions and requirements needed throughput the double-shell tank system during Phase 1 high-level waste feed delivery. This document is intended to be used by (1) the developers of the future Process Control Plan and (2) the developers of the monitoring and control system

A geostatistical method applied to the geochemical study of the Chichinautzin Volcanic Field in Mexico

Science.gov (United States)

Robidoux, P.; Roberge, J.; Urbina Oviedo, C. A.

2011-12-01

The origin of magmatism and the role of the subducted Coco's Plate in the Chichinautzin volcanic field (CVF), Mexico is still a subject of debate. It has been established that mafic magmas of alkali type (subduction) and calc-alkali type (OIB) are produced in the CVF and both groups cannot be related by simple fractional crystallization. Therefore, many geochemical studies have been done, and many models have been proposed. The main goal of the work present here is to provide a new tool for the visualization and interpretation of geochemical data using geostatistics and geospatial analysis techniques. It contains a complete geodatabase built from referred samples over the 2500 km2 area of CVF and its neighbour stratovolcanoes (Popocatepetl, Iztaccihuatl and Nevado de Toluca). From this database, map of different geochemical markers were done to visualise geochemical signature in a geographical manner, to test the statistic distribution with a cartographic technique and highlight any spatial correlations. The distribution and regionalization of the geochemical signatures can be viewed in a two-dimensional space using a specific spatial analysis tools from a Geographic Information System (GIS). The model of spatial distribution is tested with Linear Decrease (LD) and Inverse Distance Weight (IDW) interpolation technique because they best represent the geostatistical characteristics of the geodatabase. We found that ratio of Ba/Nb, Nb/Ta, Th/Nb show first order tendency, which means visible spatial variation over a large scale area. Monogenetic volcanoes in the center of the CVF have distinct values compare to those of the Popocatepetl-Iztaccihuatl polygenetic complex which are spatially well defined. Inside the Valley of Mexico, a large quantity of monogenetic cone in the eastern portion of CVF has ratios similar to the Iztaccihuatl and Popocatepetl complex. Other ratios like alkalis vs SiO2, V/Ti, La/Yb, Zr/Y show different spatial tendencies. In that case, second

Multivariate Statistical Process Control

DEFF Research Database (Denmark)

Kulahci, Murat

2013-01-01

As sensor and computer technology continues to improve, it becomes a normal occurrence that we confront with high dimensional data sets. As in many areas of industrial statistics, this brings forth various challenges in statistical process control (SPC) and monitoring for which the aim...... is to identify “out-of-control” state of a process using control charts in order to reduce the excessive variation caused by so-called assignable causes. In practice, the most common method of monitoring multivariate data is through a statistic akin to the Hotelling’s T2. For high dimensional data with excessive...... amount of cross correlation, practitioners are often recommended to use latent structures methods such as Principal Component Analysis to summarize the data in only a few linear combinations of the original variables that capture most of the variation in the data. Applications of these control charts...

The Role of Geochemical Modeling in Predicting Quality Evolution of Acid Mine Drainage

Directory of Open Access Journals (Sweden)

Andrea Šlesárová

2004-12-01

Full Text Available In recent years the massive reduction of raw materials production brings a wide scale of problems. Among the most frequent exposes of mining activities belong besides old spoil heaps and sludge lagoons, also the drainage of acidic and highly mineralized mine waters known as “the Acid Mine Drainage” (thereinafter AMD from old mine workings. The acid mine drainage presents to the surrounding environment a massive problem. These waters are toxic to the plant and animal life, including fishes and aquatic insects. The primary control of the drainage pH and the metal content is the exposure of sulphide minerals to weathering, the availability of atmospheric oxygen, and the sensitivity of non-sulphide minerals to buffer acidity. A geochemical modeling software is increasingly used to solve evolution of the complex chemical systems such as the interaction of acid mine drainage with wall rocks, migration of AMD components. Beyond the better computer facilities it allows to study of thermodynamic properties substances and to enlarge thermodynamic databases. A model is a simplified version of reality based on its observation and experiments. A goal of the modeling process is the tendency to better understand processes taking place inside of the system, the attempt to assume the system’s behaviour in the future or to predict the effect of changed conditions in the system’s environment on the system itself.

Process and research method of radionuclide migration in high level radioactive waste geological disposal system

International Nuclear Information System (INIS)

Chen Rui; Zhang Zhanshi

2014-01-01

Radionuclides released from waste can migrate from the repository to the rock and soil outside. On the other hand, nuclides also are retarded by the backfill material. Radionuclide migration is the main geochemical process of the waste disposal. This paper introduces various methods for radionuclide migration research, and give a brief analysis of the geochemical process of radionuclide migration. Finally, two of the most important processes of the radionuclide migration have been instanced. (authors)

Evaluation of uranium geochemical anomalies in the Charlotte 10 x 20 NTMS quadrangle

International Nuclear Information System (INIS)

Carpenter, R.H.

1981-11-01

This report contains a synthesis of published geological, geophysical, and geochemical information for portions of Cabarrus and Rowan Counties, NC, where uranium geochemical anomalies have been described by Heffner and Ferguson (1978). The results of a ground radiation survey in selected areas are also described. Based on an evaluation of published information and the data obtained in the field study, conclusions are made regarding the possible occurrence of uranium concentration. Recommendations for detailed surveys in certain areas are also presented

Pilot studies for the North American Soil Geochemical Landscapes Project - Site selection, sampling protocols, analytical methods, and quality control protocols

Science.gov (United States)

Smith, D.B.; Woodruff, L.G.; O'Leary, R. M.; Cannon, W.F.; Garrett, R.G.; Kilburn, J.E.; Goldhaber, M.B.

2009-01-01

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada sampled and chemically analyzed soils along two transects across Canada and the USA in preparation for a planned soil geochemical survey of North America. This effort was a pilot study to test and refine sampling protocols, analytical methods, quality control protocols, and field logistics for the continental survey. A total of 220 sample sites were selected at approximately 40-km intervals along the two transects. The ideal sampling protocol at each site called for a sample from a depth of 0-5 cm and a composite of each of the O, A, and C horizons. The Ca, Fe, K, Mg, Na, S, Ti, Ag, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y, and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO3, HClO4, and HF. Separate methods were used for Hg, Se, total C, and carbonate-C on this same size fraction. Only Ag, In, and Te had a large percentage of concentrations below the detection limit. Quality control (QC) of the analyses was monitored at three levels: the laboratory performing the analysis, the USGS QC officer, and the principal investigator for the study. This level of review resulted in an average of one QC sample for every 20 field samples, which proved to be minimally adequate for such a large-scale survey. Additional QC samples should be added to monitor within-batch quality to the extent that no more than 10 samples are analyzed between a QC sample. Only Cr (77%), Y (82%), and Sb (80%) fell outside the acceptable limits of accuracy (% recovery between 85 and 115%) because of likely residence in mineral phases resistant to the acid digestion. A separate sample of 0-5-cm material was collected at each site for determination of organic compounds. A subset of 73 of these samples was analyzed for a suite of

Uruguay Mining inventory. Las Animas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Spangenberg, J.

1981-01-01

This work is about the geochemical prospecting carried out in Las Animas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 738 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories.

Overview of geochemical modeling needs for nuclear waste management

International Nuclear Information System (INIS)

Isherwood, D.J.; Wolery, T.J.

1985-01-01

Geochemical modeling needs for nuclear waste management are discussed with an emphasis on data base development and computer code. Other areas for future research include: precipitation kinetics, fixed fugacity, sorption, glasslt. slashwater interactions, redox disequilibrium and kinetics, radiolysis, solid solutions, and isotopic fractionation. 15 references

Experimental studies on the geochemical behaviour of 54-Mn considering coastal and deep sea sediments

International Nuclear Information System (INIS)

Guegueniat, P.; Boust, D.; Dupont, J.P.; Aprosi, G.

1985-01-01

In order to study the geochemical behaviour of 54-Mn in the marine environment (Mn/sup 2+/) 200 sediments gathered in deep sea and in coastal waters were contaminated experimentally. To correlate the various results, the oxidation processes occurring with or without sediments should be specified. During this experimental work, the geochemical behaviour of manganese is dealt with using a radioactive tracer (54-Mn) in the divalent state and sediments collected on french littoral (160) in deep sea (30). The latest data published offer an excellent assessment of research findings on manganese in marine and estuary environments and testify to the interest constantly generated by this subject. It is difficult to establish a priori any predictions on the behaviour of manganese based on the properties of a given environment, notably as concerns redox conditions. The oxidation of manganese was found to be governed by a very slow autocatalysis mechanism capable of being concealed by surface catalyses on mineral phases in suspension or oxidation due to bacteria. The residence time in sea water vary considerably depending on the case from a few days to some tens of years

Snowmelt induced hydrologic perturbations drive dynamic microbiological and geochemical behaviors across a shallow riparian aquifer

Directory of Open Access Journals (Sweden)

Robert eDanczak

2016-05-01

Full Text Available Shallow riparian aquifers represent hotspots of biogeochemical activity in the arid western US. While these environments provide extensive ecosystem services, little is known of how natural environmental perturbations influence subsurface microbial communities and associated biogeochemical processes. Over a six-month period we tracked the annual snowmelt-driven incursion of groundwater into the vadose zone of an aquifer adjacent to the Colorado River, leading to increased dissolved oxygen (DO concentrations in the normally suboxic saturated zone. Strong biogeochemical heterogeneity was measured across the site, with abiotic reactions between DO and sulfide minerals driving rapid DO consumption and mobilization of redox active species in reduced aquifer regions. Conversely, extensive DO increases were detected in less reduced sediments. 16S rRNA gene surveys tracked microbial community composition within the aquifer, revealing strong correlations between increases in putative oxygen-utilizing chemolithoautotrophs and heterotrophs and rising DO concentrations. The gradual return to suboxic aquifer conditions favored increasing abundances of 16S rRNA sequences matching members of the Microgenomates (OP11 and Parcubacteria (OD1 that have been strongly implicated in fermentative processes. Microbial community stability measurements indicated that deeper aquifer locations were relatively less affected by geochemical perturbations, while communities in shallower locations exhibited the greatest change. Reactive transport modeling of the geochemical and microbiological results supported field observations, suggesting that a predictive framework can be applied to develop a greater understanding of such environments.

Snowmelt induced hydrologic perturbations drive dynamic microbiological and geochemical behaviors across a shallow riparian aquifer

Science.gov (United States)

Danczak, Robert; Yabusaki, Steven; Williams, Kenneth; Fang, Yilin; Hobson, Chad; Wilkins, Michael

2016-05-01

Shallow riparian aquifers represent hotspots of biogeochemical activity in the arid western US. While these environments provide extensive ecosystem services, little is known of how natural environmental perturbations influence subsurface microbial communities and associated biogeochemical processes. Over a six-month period we tracked the annual snowmelt-driven incursion of groundwater into the vadose zone of an aquifer adjacent to the Colorado River, leading to increased dissolved oxygen (DO) concentrations in the normally suboxic saturated zone. Strong biogeochemical heterogeneity was measured across the site, with abiotic reactions between DO and sulfide minerals driving rapid DO consumption and mobilization of redox active species in reduced aquifer regions. Conversely, extensive DO increases were detected in less reduced sediments. 16S rRNA gene surveys tracked microbial community composition within the aquifer, revealing strong correlations between increases in putative oxygen-utilizing chemolithoautotrophs and heterotrophs and rising DO concentrations. The gradual return to suboxic aquifer conditions favored increasing abundances of 16S rRNA sequences matching members of the Microgenomates (OP11) and Parcubacteria (OD1) that have been strongly implicated in fermentative processes. Microbial community stability measurements indicated that deeper aquifer locations were relatively less affected by geochemical perturbations, while communities in shallower locations exhibited the greatest change. Reactive transport modeling of the geochemical and microbiological results supported field observations, suggesting that a predictive framework can be applied to develop a greater understanding of such environments.

Geomorphic and geochemical controls on leaf wax biomarker transport and preservation in alluvial river systems: Rio Bermejo, Argentina

Science.gov (United States)

Repasch, M. N.; Sachse, D.; Hovius, N.; Scheingross, J. S.; Szupiany, R. N.

2017-12-01

Rivers are the primary conduits for organic carbon (OC) transfer from vegetation-rich uplands to long-term sinks, and thus are responsible for significant fluxes among different reservoirs of the carbon cycle. Fluxes of terrestrial OC out of river systems are generally less than fluxes into the systems, indicating loss of OC either during active fluvial transport, during residence in the active channel belt, or in older deposits outside of the active channel belt. Sedimentary biomarkers can be used to elucidate the mechanisms of transport, preservation, and/or transformation of OC during its passage from source to sink. In this study we evaluate the influence of fluvial sediment transport on preservation of terrestrial leaf wax n-alkanes. Our natural laboratory is the Rio Bermejo in northern Argentina, which transports sediment and organic matter from the central Andes over 700 km across the foreland basin without input of foreign material from tributaries. Rapid channel migration rates in a region of flexural foreland basin uplift (the forebulge) are responsible for remobilization of floodplain sediment and terrestrial OC. By sampling suspended sediment, river bank sediment, and soil from several locations along the length of the Rio Bermejo, and analyzing the dissolved chemistry, biomarker composition, and compound-specific stable isotopes, we can evaluate the geomorphic and geochemical processes that act to influence the preservation of terrestrial biomarkers through the river system. Data suggest that concentrations of long-chain terrestrial (C25-C33) alkanes decrease downstream, while concentrations of short-chain (C15-C19) alkanes increase. This trend is corroborated by a downstream increase in suspended sediment δ13C values, suggesting a replacement of terrestrial OC by microbial OC. It is likely that microbial degradation is responsible for loss of terrestrial biomarkers as their residence time in the river system increases. Controlled laboratory