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Wpływ środowiska ciekłego na trwałość betonu cementowego z kruszywem dolomitowym

Dębska D.

Ochrona przed Korozją

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2013

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nr 4

134--143

PL

Kruszywa dolomitowe poddane działaniu środowiska wilgotnego mogą ulegać rozkładowi z wytworzeniem pęczniejących wodorotlenków wapnia i magnezu. Zwiększenie wydajności reakcji dedolomityzacji wywołuje obecność w środowisku agresywnym jonów Ca2+, Mg2+ i SO4 2– oraz podwyższona temperatura. W artykule zaprezentowano wyniki badań dotyczących określenia wpływu jonów Ca2+ i zróżnicowanej temperatury na trwałość kruszyw dolomitowych oraz wyniki badań prowadzących do określenia wpływu warunków środowiskowych na podatność kruszyw węglanowych na procesy pęcznienia w alkalicznym środowisku betonów cementowych.

EN

Dolomite aggregates exposed to a wet environment may decompose and produce bulking of calcium and magnesium hydroxides. The presence of Ca2+, Mg2+ and SO42–ions in the corrosive environment and the higher temperature increase the rate of dedolomitisation. The paper presents the results of a study on the impact of the Ca2+ ions and different temperature on the durability of dolomite aggregates and of a study on the impact of exposure to such an environment on the susceptibility of carbonate aggregates to bulking in alkaline environment of cement concrete.

2

Geochemistry and age of groundwater in a hydrochemically diversified aquifer (Permo-Carboniferous, the Intra-Sudetic Synclinorium, SWPoland) derived from geochemical modelling and isotopic studies

Dobrzyński D.

Acta Geologica Polonica

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2009

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Vol. 59, no. 3

371-411

EN

Comprehensive investigations of groundwater were performed in a sedimentary aquifer of Permo-Carboniferous, Intra-Sudetic Synclinorium, in SWPoland. The investigation included aqueous chemical and isotopic composition, chemistry of mineral phases, geochemical modelling, and tritium and radiocarbon groundwater dating. Chemical diversity in the groundwater system is created by the mixing of modern fresh water and older sulphate water with higher dissolved solids. The system is treated as a system of flows of two end-member water types. Geochemical modelling is used for: (1) explaining the origin of the chemistry of both water components, (2) quantifying the groundwater mixing, (3) correcting the radiocarbon age of the groundwater for the effects of chemical water-rock interactions, and (4) calculating reaction rates. Study of stable (C, S, O, H) and unstable ([^3H], [^14]C) isotopes allowed the inverse mass balance geochemical models to be verified and specified, and the groundwater to be dated. The chemistry of the modern, tritium-bearing, fresh water is a result of dissolution of limestones, dolomites and gypsum. The mean tritium-age of this water, based on the lumped-parameter approach, varies between 10 and 200 years. The sulphate mineral water owes its chemistry to the process of dedolomitization driven by gypsum dissolution. Its radiocarbon age is about 5.9 ka BP, i.e., during theMid-Holocene Climatic Optimum. Rates of chemical reactions responsible for the formation of sulphate type water are estimated to be: dissolution of gypsum (2.85 [mi]mol/L/year) and dolomite (0.21 [mi]mol/L/year), calcite precipitation (0.20 [mi]mol/L/year), organic matter decomposition (0.08 [mi]mol/L/year).

3

Chemical diversity of groundwater in the Carboniferous-Permian aquifer in the Unisław Śląski - Sokołowsko area (the Sudetes, Poland); a geochemical modelling approach

Dobrzyński D.

Acta Geologica Polonica

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2007

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Vol. 57, no. 1

97-112

EN

Groundwater in the Carboniferous.Permian sedimentary aquifer in the vicinity of Unisław Śląski - Sokołowsko (Intra-Sudetic Basin, the Sudetes, SW Poland) manifests spatial chemical diversity. The water chemistry varies from fresh calcium-magnesium-bicarbonate groundwater at the recharge area to calciumsodium-sulphate mineral water downwards the basin. Geochemical mass balance modelling confirms that the main chemistry features of the sulphate mineral water are controlled by dedolomitization and calcium common-ion effects. Congruent dissolution of gypsum promotes incongruent dissolution of dolomite with calcite precipitation. Cation exchange between Ca[^2+] (and Mg[^2+]) solutes and Na[^+] (and K[^+]) also takes place. The sulphate mineral water shows elevated concentrations of numerous trace elements. Iron, zinc and manganese originate from dissolution of carbonates (dolomite and/or siderite) and/or sulphides. The hydrogeological system studied should be considered as a series of individual flow systems. The results of preliminary geochemical modelling corroborate the role of mixing in the formation of the spatial pattern of the aqueous chemistry in the system. The main factor that controls groundwater chemistry is the mixing of two components: modern (tritium-bearing) fresh water and older (pre-bomb Holocene) sulphate mineral water.

4

Dedolomityzacja w górnojurajskich skałach węglanowych z okolic Krakowa

Vierek A.

Przegląd Geologiczny

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2005

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Vol. 53, nr 2

156--161

EN

The Upper Jurassic limestones in the vicinity of Cracow underwent extensive dedolomitization process. Petrographic and cathodoluminescent analyses of carbonates in four test areas confirm the dedolomitization as have been developed with various intensity. The alteration of dolomite into calcite occurs as centripetal and centrifugal dedolomitization. Both processes lead finally to a complete disintegration of the dolomite crystals; calcite pseudomorphs after dolorhombs are the end products. These calcite pseudomorphs are abundant in limestones of St. Anna Mt. and in the Kostrze quarry, but are scarce in the Twardowski Cliffs area and in the outcrop of Księża Mt., which indicates a less advanced and slower dedolomitization process in the latter two areas. Most probably the initiation of dedolomitization started from the moment when a carbonate bank emerged from the sea water (Vierek, 2003); temperature of mixing fluids decreased considerably, whereas Ca 2+/Mg+- ratio in the same fluids increased.