Sample records for carnallite
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Spectrochemical determination of impurities and noble metal traces in carnallite
International Nuclear Information System (INIS)
Goldbart, Z.; Carmi, U.; Harrel, A.
1978-02-01
A spectrochemical method was developed for the determination of impurities and noble metal traces in carnallite by DC arc excitation. The investigated sample is brought to a standard form of potassium-magnesium sulphate mixed with graphite. Detection limits of 1-10 ppm were determined for 27 elements; the dynamical detection range is 1-400 ppm
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International Nuclear Information System (INIS)
Dobrunov, Yu.V.; Volynskij, V.V.; Kolobov, G.A.; Kuznetsov, S.I.
1977-01-01
Corrosion tests of titanium alloys VTI-0, OT4, VT5-1 and steel Kh18N1OT in 10% and 18% HCl with additions of carnallite at 40 deg C have been carried out. It has been established that titanium alloys in 10% and 18% HCl containing 5 and 10% carnallite are sufficiently corrosion resistant in the presence of 0.1-1% FeCl or HNO 3 and can be used for manufacturing the equipment of recirculation gas scrubbers. Steel Kh18N10T is unstable in all the media tested. It is subjected to intensive pitting. Specimens of steel Kh18N10T have also revealed edge cracking
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Energy Technology Data Exchange (ETDEWEB)
Yu, Xudong; Yin, Qinghong; Jiang, Dongbo; Zeng, Ying [Chengdu University of Technology, Chengdu (China)
2014-06-15
The metastable equilibrium of the system contained with lithium, potassium, magnesium, and chloride in aqueous system was investigated at 323 K using an isothermal evaporation method. The isothermal experimental data and physicochemical properties, such as density and refractive index of the equilibrated solution, were determined. With the experimental results, the stereo phase diagram, the projected phase diagram, the water content diagram and the physicochemical properties versus composition diagrams were constructed. The projected phase diagram consists of three invariant points, seven univariant curves and five crystallization fields corresponding to single salts potassium chloride (KCl), lithium chloride monohydrate (LiCl·H{sub 2}O), bischofite (MgCl{sub 2}·6H{sub 2}O) and two double salts lithium carnallite (LiCl·MgCl{sub 2}·7H{sub 2}O) and potassium carnallite (KCl·MgCl{sub 2}·6H{sub 2}O). Salt KCl has the largest crystallization region; it contains almost 95% of the general crystallization field.
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Mineral resource of the month: magnesium
Kramer, Deborah A.
2012-01-01
Magnesium is the eighthmost abundant element in Earth’s crust, and the second-most abundant metal ion in seawater. Although magnesium is found in more than 60 minerals, only brucite, dolomite, magnesite and carnallite are commercially important for their magnesium content. Magnesium and its compounds also are recovered from seawater, brines found in lakes and wells, and bitterns (salts).
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International Nuclear Information System (INIS)
Andrade, L.L.; Minzl, E.
1984-01-01
X-ray fluorescence spectrometry after ammonium pyrrolidinedithiocarbamate (APDC) preconcentration is proposed for the determination of nickel in chloralkali electrolysis brines. The optimum conditions for the precipitation target tube, peak intensity, background, analysing crystal, counters and exposure time were investigated. The method was applied to chloralkali brines of evaporite salts (halite, sylvinite, carnallite and tachhydrite), sodium, potassium and magnesium salts, explored in Sergipe (Brazil), by Petrobras-Mineracao S.A.(Author) [pt
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Raith, Alexander; Urai, Janos L.
2016-04-01
During the evaporation of a massive salt body, alternations of interrupted and full evaporation sequences can form a complex layering of different lithologies. Viscosity contrasts of up to five orders of magnitude between these different lithologies are possible in this environment. During the late stage of an evaporation cycle potassium and magnesium (K-Mg) salts are precipitated. These K-Mg salts are of economic interest but also a known drilling hazard due to their very low viscosity. How up to 200m thick layers of these evaporites affect salt deformation at different scales is not well known. A better understanding of salt tectonics with extreme mechanical stratification is needed for better exploration and production of potassium-magnesium salts and to predict the internal structure of potential nuclear waste repositories in salt. To gain a better understanding of the internal deformation of these layers we analyzed K-Mg salt rich drill cores out of the Zechstein III-1b subunit from the Veendam Pillow 10 km southeast of Groningen, near the city Veendam in the NE Netherlands. The study area has a complex geological history with multiple tectonic phases of extension and compression forming internal deformation in the pillow but also conserving most of the original layering. Beside halite the most common minerals in the ZIII-1b are carnallite, kieserite, anhydrite and bischofite alternating in thin layers of simple composition. Seismic interpretation revealed that the internal structure of the Veendam Pillow shows areas, in which the K-Mg salt rich ZIII 1b layer is much thicker than elsewhere, as a result of salt deformation. The internal structure of the ZIII-1b on the other hand, remains unknown. The core analysis shows a strong strain concentration in the weaker Bischofite (MgCl2*6H20) and Carnallite (KMgCl3*6H20) rich layers producing tectonic breccias and highly strained layers completely overprinting the original layering. Layers formed by alternating beds
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New data on the Geochemistry of Gases in the Potash Deposits
Directory of Open Access Journals (Sweden)
I. I. Chaykovskiy
2014-12-01
Full Text Available The composition of the gas phase of salt rocks from a number of potash deposits located in Europe (Verkhnekamskoe, Starobinskoe and Asia (Tubegatanskoe, Zhylyanskoe Satimolinskoe was studied. It allowed dividing them into two groups. In Asian deposits, only authigenic dry gases were formed by diagenetic decomposition of organic matter. Structural exposure of these deposits led to the oxidation of methane and hydrogen and enrichment by carbon dioxide. European deposits were not structurally exposed to the oxidation process, but were exposed during salt rock formation. They experienced influx of heavy hydrocarbons from the underlying strata. The history of the formation of gas regime at the Verkhnekamskoe potash deposit could be divided into three stages. First stage may be characterized by a syngenetic capture of deep gases and authigenic organic matter converted during diagenesis to methane, which percentage gradually increases with an increase of the thickness of impermeable salt strata. Then the deep gases invaded the salt formation during sedimentation of the upper carnallite layers and top salt rock. Third stage was associated with folding processes accompanied by a mobilization of fluids scattered in the gas-fluid inclusions, and with probable influx of heavy hydrocarbons and carbon dioxide resulted in formation of the secondary salt zones. Replacement of carnallite layers leads to the release of isomorphous ammonium ion and formation of a hydrogen.
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The geological and material investigation programme
International Nuclear Information System (INIS)
Joshi, A.V.
1982-01-01
The radioactive waste disposal problem is an interdisciplinary problem. The geological formation cannot be considered on its own, but must also be considered in connection with the engineering design of the disposal facility. Engineering design including the encapsulation of the glass in a 15 cm thick steel cylinder and a minimum 40 year cooling time ensures low temperatures in the salt-steel interface. Even if large quantities of carnallite were found 3.5 m away from the sides of the borehole, the temperature at 2500 m depth after taking into account temperature increase from radioactive waste will not release crystal water from the carnallite. Anhydrite layers, which may be found in the neighbourhood of Erslev 2 and at the depths contemplated for radioactive waste disposal, will not be continous, but only in the form of blocks of limited lengths. They cannot therefore form a passage to a water bearing aquifer. The volume of salt necessary for waste disposal - including a 200 m safety barrier - is less than 2 km 3 . The Mors dome with a salt volume of about 264 km 3 provides a very substantial safety margin. The geological investigations have fulfilled the purpose of the present phase of investigations and show the Mors salt dome to be a suitable dome for disposal of high-level radioactive waste. (EG)
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Energy Technology Data Exchange (ETDEWEB)
Voss, Ina
2015-07-16
The research platform ENTRIA (Disposal options for radioactive residues Interdisciplinary analyses and development of evaluation principles) includes the sub-project ''Final disposal in deep geological formations without any arrangements for retrieval''. This approach considers rock salt (beside clay and granite) as host rock formation for disposal of heat-producing long-live waste. Most rock salt formations contain Mg-rich brines derived from highly evolved sea water evaporation processes now included in the rock salt mass. If such brines get access to metal-canister corrosion will allow release of soluble nuclides to the brine. In this scenario, it cannot be excluded that contaminated brines leave the deep seated disposal area and move along geological or technical migration pathways towards the rock salt/cap rock contact. The temperature of the brine will drop from near 80 C to 25 or 30 C. The deceasing temperature of the brine causes precipitation of magnesian chloride and sulfate phase in equilibrium with the brine. In order to understand the salt precipitation and the retention mechanism of dissolved trace elements experiments have been set up which allow formation of sylvite, carnallite, kainite, and hydrous Mg-sulphates under controlled conditions. The retention capacity of crystallizing salt minerals based occurring in magnesian brine solutions at decreasing temperature within a salt dome is best measured as the distribution coefficient D. This concept assumes incorporation of trace elements into the lattice of salt minerals. The distribution coefficients of the trace elements, Rb, Cs, Co, Ni, Zn, Li and B between sylvite, carnallite, kainite, and MgSO{sub 4} phases have been determined at experimental temperatures of 25, 35, 55 and 83 C. The results clearly indicate the following range of distribution coefficients (D): Sylvite D > 1 Rb and Br, D < 1 Co, Ni, Zn, Li and B, Carnallite D > 1 Rb and Cs, D < 1 Co, Ni, Zn, Li and B, Kainite D
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Chemical modeling of nuclear waste repositories in the salt repository project
International Nuclear Information System (INIS)
Jansen, G.; Raines, G.E.; Kircher, J.F.; Hubbard, N.
1985-01-01
Salt deposits contain small amounts of water as brine in fluid inclusions in halite and in hydrous minerals, e.g., clays, kieserite (MgSO 4 . H 2 O) and carnallite (KMgCl 3 . 6H 2 O). For the candidate salt deposits, the total amounts of water as volume % brine are: Palo Duro Basin, Texas, approximately 1.8; Paradox Basin, Utah, approximately 5.0 for the carnallite-marker zone, and less than approximately 0.5 below this zone; Gulf Coast salt domes, less than 0.15. For the Palo Duro and Paradox salt, the brines are Mg-rich (approximately 20,000 mg/L to approximately 100,000 mg/L) and sometimes Ca-rich (up to about 20,000 mg/L) NaCl brines. Brine migration calculations have been made using calculations of the time-variant thermal gradient around the waste packages and conservatively high brine volumes in the salt (5.0 volume % for the Texas and Utah sites and 0.5 volume % for the Gulf Coast) as input data. The maximum amounts of brine that eventually migrate to each waste package are about 1.0m 3 (for 5.0 volume % brine) and 0.2m 3 (for 0.5 volume % brine). With current conceptual designs for waste package overpacks (10 to 15 cm thick low-carbon steel), the waste package is not breached by uniform corrosion within 10,000 years. In brines this material thus far shows only uniform corrosion. For the expected conditions, where the brine is provided solely by brine migration, the brine is consumed by reaction with the iron of the overpack nearly as fast as it migrates to the waste package. Therefore, for the expected conditions, data about corrosion rates, radiolysis, etc., are not important. However, it is essential that accurate volumes of in-migrating brine can be calculated
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Geotechnical investigations on backfill materials in the Asse salt mine
International Nuclear Information System (INIS)
Kappei, G.
1986-01-01
The compression behaviour of rock salt grit is being investigated by compression tests at the Asse salt mine. The various test parameters are introduced and their results are discussed. The permeability of rock salt grit with saturated NaCl-brine in dependency upon the grain size and compactness, resp. the porosity, is being determined at the Asse salt mine. The test equipment and the results determined here are shown. In addition to laboratory tests, geotechnical investigations are taking place in a carnallitic chamber of the Asse salt mine which had been backfilled in earlier years. They chiefly concern measurements of the deformation rates in drifts - which were mined between the chambers in remaining pillars - as well as horizontal deformation measurements in the backfilling. (orig./DG)
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International Nuclear Information System (INIS)
Herrmann, A.G.; Roethemeyer, H.
2007-01-01
Reliable safety assessments of underground deposits require the respective geological systems to be observed and evaluated in their entirety. Important objects to be studied for this purpose are observations of nature providing information about the natural isolation potential. The study under review presents 5 such observations of nature in the geosystem of the Gorleben salt dome. They include the absolute Br-distribution in carnallite rock and in Stassfurt-type rock salt (in a profile and in space), the quantitative chemical compositions of minor fluid inclusions in salt crystals and of residual fluid inside evaporates. All findings agree in one respect: In the central part of the salt dome explored so far, no influences have been active, from the origins of the evaporates some 250 million years ago to this day, which were imposed from the outside (such as solutions from the caprock, the adjoining rock) and/or have given rise to large-scale changes in the mineralogical and chemical compositions of the saline rock. (orig.)
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Extractive process for preparing high purity magnesium chloride hexahydrate
Directory of Open Access Journals (Sweden)
Fezei Radouanne
2012-01-01
Full Text Available This paper refers a method for the preparation of magnesium chloride hexahydrate (bischofite from Sebkha el Melah of Zarzis Tunisian natural brine. It is a five-stage process essentially based on crystallization by isothermal evaporation and chemical precipitation. The two first steps were dedicated to the crystallization of sodium chloride and potassiummagnesium double salts, respectively. Then, the resulting liquor was desulfated using calcium chloride solution. After that another isothermal evaporation stage was implemented in order to eliminate potassium ions in the form of carnallite, KCl.MgCl2.6H2O. At the end of this step, the recovered solution primarily composed of magnesium and chloride ions was treated by dioxan in order to precipitate magnesium chloride as MgCl2.6H2O.C4H8O2. This compound dried at constant temperature of 100°C gave good quality magnesium chloride hexahydrate. Besides this salt, the various by-products obtained from the different treatment stages are also useful.
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Mineralogical aspects of fluid migration in the Salt Block II experiment
International Nuclear Information System (INIS)
Lambert, S.J.
1980-05-01
A block of evaporite rock containing the mineral assemblage halite (88%) - polyhalite (8%) - sylvite (4%) was machined into a cylinder one meter in diameter and one meter high, and was fitted with an axial heater, thermocouples and an off-gas collection system. After about 100 days of heating, identification of mineral efflorescences at the heater hole (carnallite and bischofite) showed that a significant portion of the 111 grams of water recovered (out of around 8500 grams available in the rock) migrated as a liquid, not as a vapor. A microscopic examination of rock slices from within 15 cm of the heater hole (where the temperature was 100 to 200 0 C, and the gradient was 3 to 15 0 C/cm) revealed that: (1) fluid inclusions had migrated, but rarely across grain boundaries; (2) fluid inclusions had not been mobilized at distances greater than about 15 cm from the heater hole; and (3) intergranular liquid had been conspicuously mobilized within 15 cm of the heater hole
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Zechstein salt Denmark. Vol. 1
International Nuclear Information System (INIS)
Lyngsie Jacobsen, F.; Soenderholm, M.; Springer, N.; Gutzon Larsen, J.; Lagoni, P.; Fabricius, J.
1984-01-01
The Salt Research Project EFP-81 has mainly been aiming upon an elucidation of the stratigraphy of the Danish Zechstein evaporites. Also an attempt to clarify the connection between the fabric and the strength of the strongly deformed domal rock salt is performed. The unravelling of the stratigraphy is carried out by means of renewed interpretations of new and old data from all the wells drilling in the Danish Permian basin in connection with a revaluation of the core descriptions. By means of trace elements analysis it is possible to some extent to distinguish between Zestein 1 and 2 ''grey salt''. A description of the transition zone between Zechstein 1 and 2 is carried out. New methods of fabric analyses are introduced and the strength measurements of the rock salt are treated statistically in connection with new defined rock salt parameters. An investigation of fluid inclusions in halite and quartz crystals from dome salt has resulted in the determination of salinity and chemical composition of the brines present in the salt. Temperatures and corresponding pressures during the evolution of the salt pillow and salt dome have been established. The dehydration conditions of natural carnallite in situ are clarified. (author)
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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.
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Long term mineralogical changes in salt formations due to water and brine interactions
International Nuclear Information System (INIS)
Herbert, H.J.; Brewitz, W.
1996-01-01
Four very common long term mineralogical changes in salt formations are discussed in the view of the safety considerations for underground repositories. Two of these processes, the 'Hartsalz' and 'Carnallite' dissolution were studied in two scale in situ experiments. The results are presented and compared with the results of the geochemical modelling with the computer code EQ3/6. Furthermore the reactions leading to the formation of the gypsum cap rock on the top of the Zechstein salt formations and to the polyhalitization of anhydrite are discussed. Geological field observations and mineral assemblages agree well with the results of the geochemical modelling employing the Pitzer formalism along with the Harvie, Moller and Weare database. We conclude that once the mechanisms of the chemical reactions are well understood it becomes possible to evaluate realistically whether such processes, when encountered in the repository, are still active or whether they are finished. It also becomes possible to estimate the volume changes associated with the reactions and thus the impact of these reactions on the integrity and the geomechanical stability of the salt formation. The intimate knowledge of the reaction mechanisms of the short and long term changes in the mineralogical assemblages and the associated brine chemistry is a first prerequisite for the correct evaluation of the origin of brines. Thus, it is essential for the correct assessment of the hazards which brine inflows may pose for the safety of a repository in salt formations. (authors). 8 refs., 14 figs., 8 tabs
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Trial storage of high-level waste cylinders in the Asse II salt mine
International Nuclear Information System (INIS)
1984-01-01
This report covers the contract period 1976-77, as well as some of the tasks carried out during the extension in 1978, in the framework of the R and D programme for disposal of radioactive waste in salt formations. With regard to the in-situ tests for the liberation and migration of brine, the testing devices were examined successfully. Laboratory examinations carried out showed a stepwise liberation of the water contents in halite in dependence on the temperature. The amount of brine liberated stood in good agreement with the in situ results. A temperature test for borehole convergence resulted in definite convergence rates. Simultaneously no influence was registered in the stability of the surrounding rocks. For the realization of an integrated major experiment, temperature test field IV was mined on the 750 m level of the Asse Salt Mine and heater- as well as measurement drillings were carried out. Extensive rheological examinations are concentrated particularly on the halite and secondly on the Carnallite. They are chiefly based on uni- and multiaxial pressure tests. Computer programmes are developed to examine the heat generation in wastes as well as in salt. In comparison, the programme development of computer codes for the stability behaviour of rocks is still at a relatively early stage, because it has to build up on the results of heat generation. The works for the development of a transport container with a shielding combination are at a very advanced stage. An integrated disposal- and retrieval system was developed, tested and successfully demonstrated. A monitoring system in the mine has also been developed in its essential parts
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International Nuclear Information System (INIS)
Diem, W.
1985-01-01
The Stassfurt rock salt (Na2) in the Asse II salt mine constitutes a saline sequence of the sub-Hercynian basin. In the anticline of the Asse II the Na2 constitutes a core of the anticline with an interior special folding. The combination of underground mapping with the investigations of the salt petrography permits the recognition of stratigraphic unities and with it sedimentary and early diagenetic formation processes for the stratigraphic beds of the Hauptsalz (Na2β), the Speisesalz (Na2SP) and the Polyhalitbaenkchensalz (Na2P). An additional postdiagenetic new formation of minerals from the overlying Stassfurt potash layer (K2C) can be recognized in the kieseritic region of the ''Carnallitisch-Kieseritische Ueberganssalz (Na2K+C)'' and in the ''Tonliniensalz'' (Na2TL). The lower part of the Na2β belongs to a saline basin facies. In the upper part of the Na2β structural and textural characteristics refer to the swallowing of the saline sedimentation room. Simultaneously, more and more terrestrial influences of the saline sedimentation become conspicuous in the northwestern part of the Asse II. They have their clearest facies in the only locally formed Tonliniensalz (Na2TL). The petrographic review of the ''polyhalite region'', which encloses the upper part of the Na2β, the Na2SP and the Na2P, rendered obvious indications for a pseudomorphic origin of polyhalite from primarily sedimened gypsum. The replacement of anhydrite by polyhalite was compared to it as being of unimportant significance. The quantitative parts of the accessory minerals (polyhalite, anhydrite, kieserite, sylvite, carnallite) were determined by means of geochemical investigations in the stratigraphic horizons of Na2 in the mine Asse II. A regional comparison with the saline sedimentation of Zechstein 2 in the sub-Hercynian basin shows a progressive saline sedimentation cycle of the Stassfurt type for the fine stratigraphic division of the Na2 in Asse II. (orig./HP) [de
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Cocker, Mark D.; Orris, Greta J.; Dunlap, Pamela; Lipin, Bruce R.; Ludington, Steve; Ryan, Robert J.; Słowakiewicz, Mirosław; Spanski, Gregory T.; Wynn, Jeff; Yang, Chao
2017-08-03
stratabound Famennian tract in the Dnieper-Donets Basin could contain significant undiscovered potash resources.The Cisuralian evaporite sequence in the Dnieper-Donets Basin consists of 10 evaporite cycles with the upper 3 cycles containing potash-bearing salt (mainly as sylvite and carnallite) in several subbasins and polyhalite in the sulfate bearing parts of the identified tract. The area of the Cisuralian tract is 62,700 km2. Potash-bearing cycles are as much as 40 m thick. One subbasin is reported to contain 794 million metric tons of “raw or crude” potash-bearing salt which could contain 50 to 150 million metric tons of K2O, depending on the grade. Undiscovered potash resources in the remainder of this permissive tract may be significantly greater. Depths to the Permian salt range from less than 100 to about 1,500 m.Undiscovered resources of halokinetic potash-bearing salt in the Dnieper-Donets Basin were assessed quantitatively for this study by using the standard USGS three-part form of mineral resource assessment (Singer, 2007a; Singer and Menzie, 2010). Delineation of the permissive tract was based on distributions of mapped halokinetic salt structures. This tract contains at least 248 diapiric salt structures with a total area of 7,840 km2 that occupies approximately 8 percent of the basin area. The vertical extent of these salt structures is hundreds of meters to several kilometers. This assessment estimated that a total mean of 11 undiscovered deposits contain an arithmetic mean estimate of about 840 million metric tons of K2O in the halokinetic salt structures of the Dnieper-Donets Basin for which the probabilistic estimate was made.