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    Wyświetlanie 1-8 z 8
    Tytuł:
    Department of Mineralogy, Petrography and Geochemistry
    Autorzy:
    Matusik, J.
    Rzepa, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/184452.pdf
    Data publikacji:
    2016
    Wydawca:
    Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Wydawnictwo AGH
    Tematy:
    chemistry
    rock
    origin
    Źródło:
    Geology, Geophysics and Environment; 2016, 42, 2; 218-222
    2299-8004
    2353-0790
    Pojawia się w:
    Geology, Geophysics and Environment
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Geochemistry of waters and bottom sediments in landslide lakes in Babiogórski National Park
    Autorzy:
    Sala, D.
    Rzepa, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/2086539.pdf
    Data publikacji:
    2011
    Wydawca:
    Polskie Towarzystwo Mineralogiczne
    Tematy:
    bottom sediments
    water
    trace elements
    Babiogórski National Park
    Opis:
    The aim of this work was to assess the contamination of the landslide lakes located within Babiogórski National Park. For this purpose, samples of water and bottom sediment from 12 lakes were collected. Chemical analyses of the waters (including main cation and anion concentrations, trace-metal levels and selected physicochemical parameters) and of the sediments (including heavy metals) were performed. The waters are acidic to neutral and are characterized by low mineralization. Concentrations of trace elements are commonly low. Elevated levels of Fe, Mn and Al are probably related to natural geochemical processes. The sediments are strongly contaminated by Cd, whereas other trace metals levels are at their hydrogeochemical background. The high level of Cd contamination is most probably related to long-range industrial emissions.
    Źródło:
    Mineralogia; 2011, 42, 1; 63--72
    1899-8291
    1899-8526
    Pojawia się w:
    Mineralogia
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Manganese oxides from Zalas, Kraków area, southern Poland
    Autorzy:
    Polak, M.
    Gołębiowska, B.
    Rzepa, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/184692.pdf
    Data publikacji:
    2016
    Wydawca:
    Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Wydawnictwo AGH
    Tematy:
    intrusion
    volcanic rock
    limestone
    Opis:
    The Zalas quarry is located in the southern, marginal part of the Silesian-Cracovian Monocline. Permian rhyodacite laccolith has been exploited here for over 70 years. The intrusion was formed about 260–280 Ma during the Early Permian transtensional, sinistral tectonic regime predominating in central Europe at that time (Nawrocki et al. 2005). Permian volcanic rocks are overlain by a Middle–Upper Jurassic sedimentary sequence, built from sands and sandstones, substituted with the passing of time by limestones and sandy limestones rich in fossils (Matyszkiewicz et al. 2006). Quarrying operations carried out approximately 10 years ago uncovered a fault zone cutting the Middle Jurassic sandy limestones. Exposed breccias was locally encrusted by a hydrothermal mineralization forming thin veinlets cutting the limestone, or surrounding the breccia clasts. Primary mineralization contained small relics of pyrite, chalcopyrite, chalcocite, galena, native bismuth and barite and was significantly replaced by supergene minerals e.g. Fe and Mn oxides, malachite, cuprite, Cu sulphates, iodargyrite, Bi oxychlorides and Na, K chlorides (Gołębiowska et al. 2006, 2010, 2015). The mineralization is most likely connected with rejuvenation of Early-Paleozoic fault zones during the Sava phase of the Alpine orogeny, and subsequent intensive weathering under semi-arid and arid climate in a period between the Oligocene and Middle Miocene (Gołębiowska et al. 2010). In the sandy limestone encrusted by the oxidized mineralization, very interesting Mn-oxides, enriched in numerous heavy metals were encountered. They filled small fractures and voids within the fault breccia. Among them, Tl-rich varieties have been recently reported. Extremely high thallium content, reaching 20.82 wt% Tl 2 O, makes the oxides unique on a world scale (Gołębiowska et al. 2015). In this paper we focused on the variable admixtures in Mn oxides from oxidation zone in Zalas; for this purpose, SEM-EDS and WDS analyses were carried out. Mn oxides in Zalas are accompanied by malachite, Fe oxides (goethite and hematite) and relics of primary mineralization (Matyszkiewicz et al. 2015). Mn and Fe oxides commonly form the yellowish to red-brownish or black tiny grains or cryptocrystalline aggregates with sizes up to a few millimetres across. Manganese oxides contain variable admixtures of Cu, Ca, Pb, Ba, Fe, Ni, Co and Tl. On the basis of chemical analyses, three major Mn oxide types have been distinguished: those enriched in (i) Ni and Co, (ii) Pb and (iii) Ba and Ca. Co-Ni-bearing Mn oxides, probably asbolane-type, contain 17.01–21.58 wt% CoO and 3.05–8.33 wt% NiO. These phases contain also admixtures of Cu (up to 10 wt% CuO) and Al (up to 7 wt% of Al 2 O 3 ), as well as traces of Fe, Ba, Zn, Mg and Tl (up to 0.5 wt%). Interestingly, in Mn oxides of this type, the admixtures of lead are absent. Pb-bearing Mn oxide, probably coronadite, contain up to 21.48 wt% PbO. In its composition various other elements were also noticed: up to 2 wt% CoO, 0.4 wt% NiO and very high concentrations of CuO up to 8 wt%, as well as up to 1 wt% BaO, FeO, CaO Tl 2 O, Al 2 O 3 and traces of Zn and Mg. Chemical mapping indicates that the Ba- or Ca-bearing Mn oxides occur only in marginal parts of zoned MnO 2 aggregates with almost pure MnO 2 in their cores. They contain 78–84 wt% MnO 2, 3–10 wt% BaO and 2.5–4.5 wt% CaO. High contents of Co, Ni, Pb, Cu and Tl in Mn oxides from Zalas indicate a direct link with the primary ore assemblage. High concentration of cobalt and nickel might suggest some connection with Co and Ni mineralization known from nearby Karniowice Travertine (Czerny 1992). Mineral association, as well as crystal morphologies and sizes could indicate hydrothermal origin of at least part of the Mn oxides. However, identification of the particular minerals as well as concluding on the details of their origin is quite difficult on this stage of research.
    Źródło:
    Geology, Geophysics and Environment; 2016, 42, 1; 120-121
    2299-8004
    2353-0790
    Pojawia się w:
    Geology, Geophysics and Environment
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Microbiology of acid waters ans ferruginous precipitates formation in the polish part of the Muskau Arch - preliminary raport
    Mikrobiologia kwaśnych wód a tworzenie się żelazistych osadów w polskiej częsci Łuku Mużakowa - wstępne wyniki
    Autorzy:
    Bożęcki, P.
    Rzepa, G.
    Ratajczak, T.
    Powiązania:
    https://bibliotekanauki.pl/articles/395757.pdf
    Data publikacji:
    2010
    Wydawca:
    Uniwersytet Zielonogórski. Oficyna Wydawnicza
    Tematy:
    kwaśne wody
    osady żelaziste
    Łuk Mużakowa
    AMD environment
    pyrite oxidation
    Muskau Arch
    schwertmannite
    goethite
    jarosite
    microbiological variability
    Opis:
    This work presents preliminary results of mineralogical, geochemical and microbiological investigations carried out in the Polish part of the Muskau Arch. As a result of sulphide oxidation in this abandoned mining area, highly acidified Fe-rich waters have been formed. Ferruginous precipitates composed mainly of schwertmannite, goethite, jarosite and gypsum accompany them. Both the water chemistry and the rate of the sediments formation vary significantly due to seasonal weather changes and microbiological activity.
    W pracy przedstawiono wstępne wyniki badań mineralogicznych, geochemicznych i mikrobiologicznych wykonywanych w polskiej części Łuku Mużakowa. W wyniku utleniania siarczków w tym opuszczonym obszarze górnictwa tworzą się wody bardzo zakwaszone oraz bogate w żelazo. Osady żelaziste składają się głównie z schwertmannitu, goethytu, jarosytu oraz gipsu. Zarówno chemia wody oraz tempo powstawania osadów różnią się znacząco ze względu na sezonowe warunki pogodowe i aktywność mikrobiologiczną.
    Źródło:
    Civil and Environmental Engineering Reports; 2010, 4; 13-18
    2080-5187
    2450-8594
    Pojawia się w:
    Civil and Environmental Engineering Reports
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Results of microbiological research in the polish part of the Muskau Arch - the largest AMD environment in Poland - final report
    Wyniki badań mikrobiologicznych prowadzonych w zbiornikach kwaśnych wód kopalnianych w polskiej części Łuku Mużakowa – największym tego typu środowisku w Polsce
    Autorzy:
    Bożęcki, P.
    Rzepa, G.
    Ratajczak, T.
    Powiązania:
    https://bibliotekanauki.pl/articles/395915.pdf
    Data publikacji:
    2014
    Wydawca:
    Uniwersytet Zielonogórski. Oficyna Wydawnicza
    Tematy:
    AMD environment
    Muskau Arch
    microbiological variability
    środowisko AMD
    Łuk Mużakowa
    zmienność mikrobiologiczna
    Opis:
    This work presents the results of microbiological investigations carried out in the Polish part of the Muskau Arch. In this abandoned lignite mining area highly acidified Fe-rich waters have been formed as a result of sulphide oxidation. Microbiological tests have shown that all studied groups of microorganisms exhibit both time and spatial variability. The most common group of microorganisms are bacteria Galionella sp.
    W rejonie Łuku Mużakowa prowadzona była eksploatacja m.in. węgla brunatnego. Działalność kopalń w tym rejonie trwała do końca lat 70. XX wieku. Po zakończeniu eksploatacji w obniżeniach terenu powstały liczne zbiorniki wodne, tworzące tzw. pojezierze antropogeniczne. W wyniku utleniania siarczków (głównie pirytu) występujące tutaj wody są bogate w żelazo oraz charakteryzują się bardzo niskim pH. W pracy przedstawiono wyniki badań mikrobiologicznych wykonywanych w polskiej części tej struktury geologicznej. Stwierdzono, że wszystkie badane grupy mikroorganizmów wykazują zmienność zarówno czasową (wynikającą z pór roku) jak i przestrzenną (wynikającą z miejsca pobrania próbki do badań). Wykazano, iż najliczniejszą grupą mikroorganizmów są nitkowate bakterie z rodzaju Gallionella. Stosunkowo liczne są ponadto bakterie Acidithiobacillus ferrooxidans. Ponieważ obie te grupy mikroorganizmów do swojego wzrostu potrzebują tych samych związków chemicznych ich populacje konkurują ze sobą – nawet kosztem ograniczenia tempa rozwoju populacji własnego gatunku.
    Źródło:
    Civil and Environmental Engineering Reports; 2014, 12; 17-26
    2080-5187
    2450-8594
    Pojawia się w:
    Civil and Environmental Engineering Reports
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Arsenic interactions with bog iron ores – As(III) and As(V) adsorption-desorption study
    Autorzy:
    Tuchowska, M.
    Bajda, T.
    Rzepa, G.
    Dębiec, K.
    Drewniak, Ł.
    Powiązania:
    https://bibliotekanauki.pl/articles/184786.pdf
    Data publikacji:
    2016
    Wydawca:
    Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Wydawnictwo AGH
    Tematy:
    environment
    ground water
    toxicology
    Opis:
    Arsenic is a toxic element, elevated concentration of which in the environment can result from both anthropogenic activity and natural geochemical processes. The contamination of water, especially groundwater, with As has been recognized as a major environmental problem (Choong et al. 2007). The mobility and toxicology of As is related to its valence state which can be (+III) or (+V), depending mainly on pH and redox conditions. Because even low As concentrations in drinking water causes severe health effects, the technologies of its effective removal are thought to be very important (Mohan & Pittman 2007). Among many methods developed for removing aqueous arsenic species, the adsorption onto iron oxyhydroxides or oxyhydroxide-rich sorbents is one of the most effective. Despite many studies, the factors affecting the adsorption processes, especially those related to the sorbent properties, are still far from being fully understood (e.g. Adra et al. 2016). In this work we investigated As(III) and As(V) adsorption and desorption by bog iron ores – natural ferruginous sediments which have been recently demonstrated to exhibit very good sorption properties. For this study four samples of bog iron ores, were collected at different sites in the Polish Lowlands: Kolechowice (KOL), Biadaszki (BD), Strzyżew (ST) and Dębe Małe (DM). They represent different bog iron ore types which, in spite of having diversified structures, mineral composition and, subsequently, physical and chemical properties, revealed good sorption affinities for trace elements in previous work (Rzepa et al. 2009). In batch experiments the influence of various factors on adsorption were studied, including initial As concentrations, initial pH values and competitive adsorption of As(III) and As(V). The effect of initial As concentrations was studied in the range of 0.01–20 mM As(III) or As(V) at pH 7.5. The influence of pH was evaluated by the adsorption of 5 mM As solution in the pH range of 2–12. The experiment of competitive adsorption of arsenite and arsenate was performed for various proportion of As(III) to As(V) in the range of initial concentrations 0.025–20 mM at pH 7.5. The bonding strength of As with bog iron ore surface was estimated on the basis of three-step desorption experiments, which were conducted for the samples previously treated with As(III) or As(V) at pH 7.5 and at constant 20 mM initial concentration of arsenic. Arsenic concentrations in filtered (filter with a 0.22 μm pore size) solutions after all the experiments were analyzed using AAS and UV-Vis spectrophotometry. The results showed that arsenic sorption depends on its oxidation state. All the bog iron ores bound more As(III) than As(V). The highest amount of As(III) was sorbed by ST sample (458 mmol/kg), lower by KOL (430 mmol/kg) and DM (427 mmol/kg), and the lowest by BD (333 mmol/kg). However, in the case of As(V), the order was different: the highest amount of As was sorbed by BD sample (264 mmol/kg), lower by ST (218 mmol/kg), and the lowest by DM (163 mmol/kg) and KOL (158 mmol/kg). The highest uptake (80–95%) of As(III) was noted at lower initial concentrations, while the highest uptake (60–70%) of As(V) was observed at higher initial concentrations. As(III) sorption effectiveness was >80% throughout the pH range of 4 to 9 and was almost independent on pH in that range. In contrast, the As(V) sorption was higher at slightly acidic pH and significantly decreased in alkaline conditions. At pH around 3, sorption efficiency of both As(III) and As(V) decreased, which is likely due to the increased solubility of iron oxyhydroxides (Zeng, 2004). The results of competitive sorption experiments revealed that at low concentrations of both As species reduction of sorption efficiency of As(III) occurred. Sorption of As(V) was also affected, but only if amount of As(III) was higher than As(V). On the contrary, at high As(V) and As(III) concentrations, As(V) did not influence As(III) sorption, but As(III) substantially increased sorption of As(V). Desorption of arsenic by foreign ligands resulted in extraction of more than 70% of absorbed As(III) and As(V). In the absence of the exchange ligand, i.e., in deionized water, desorption of As(V) and As(III) was considerably lower, but noticeable. This study shows that bog iron ores are very good arsenic sorbents. However, the extent of As removal seems to be affected by various factors including As species and the composition of the ores themselves. As(V) is immobilized less effectively than As(III), and the process is influenced by pH values. It is believed, that the uptake of As by bog ores is controlled primarily by iron oxyhydroxides, as main components of these rocks, but mechanisms predominant in As(III) and As(V) adsorption are different and affected by presence of e.g. phosphate and silicate ions (Ociński et al. 2011). There are no simple correlations between mineralogy and sorption capacity. Due to the variability in chemical and mineral composition of different types of bog iron ores, various levels of arsenic removal can be obtained. Such properties of the ores, combined with their ubiquity in many near-surface environments may be regarded as an incentive for the environmental protection practice.
    Źródło:
    Geology, Geophysics and Environment; 2016, 42, 1; 133-134
    2299-8004
    2353-0790
    Pojawia się w:
    Geology, Geophysics and Environment
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Weathering in a regolith on the Werenskioldbreen forefield (SW Spitsbergen) : modelling of pore water chemistry
    Autorzy:
    Kwaśniak-Kominek, M.
    Manecki, M.
    Rzepa, G.
    Płonka, A. M.
    Górniak, D.
    Powiązania:
    https://bibliotekanauki.pl/articles/191820.pdf
    Data publikacji:
    2016
    Wydawca:
    Polskie Towarzystwo Geologiczne
    Tematy:
    retreating glaciers
    chronosequence
    hydrochemistry
    Werenskioldbreen
    Spitsbergen
    Opis:
    The mineral framework and pore waters of glacial sediments exposed in the foreland of Weren- skioldbreen in SW Spitsbergen were sampled and analyzed to model the evolution of pore water chemistry, representing the advancement of weathering in a chronosequence. Three samples were taken at distances representing snapshots of approximately 5, 45 and 70 years of exposure. Complementary mineralogical analyses of the mineral framework and chemical analyses of pore waters, coupled with thermodynamic modelling of mineral-water interactions were applied. Recently uncovered sediments of the bottom moraine underwent very little weathering underneath the glacier cover; both the sediments and pore waters in the forefield of the Werenskioldbreen represent a very immature system. Poorly sorted sediments were deposited by the glacier and not reworked by fluvioglacial waters. The ratio of ‘amorphous iron’ to ‘free iron’ Feo/Fed increases with distance from the glacier terminus from 0.30 through 0.36 to 0.49, typical for fresh glacial till. The increase in saturation with CO2 (from p(CO2) –3.8 to –2.4) and the concentration of all major ions in pore waters (from 123 to 748 mg/L total dissolved solids, TDS) was observed in this young chronosequence. The waters evolved from carbonate- dominated to sulphate-dominated, indicating that with progress in weathering the dominating processes are equilibration with carbonates, oxidation of sulphides and the influence of gypsum precipitation by seasonal freeze-thaw cycles. Mass balance calculations and inverse modelling of the composition of pore waters, verified by microscopic observations of alteration on the surfaces of mineral grains, allowed thermodynamic confirmation of the fact that the relative significance of carbonate weathering decreases and that of sulphate increases down the chronosequence. The participation of silicate minerals in weathering is low, indicating a relatively immature stage of weathering within this particular chronosequence. It is significant that the morphology of etch pits and the formation of secondary phases apparent on mineral surfaces were identical, regardless of the distance from the glacier terminus. This might indicate that the mechanisms of particular weathering processes at the mineral-water interface are the same at the initial as well as at the more mature stages and do not change at least within ca. 70 years of exposure.
    Źródło:
    Annales Societatis Geologorum Poloniae; 2016, 86, 3; 249-264
    0208-9068
    Pojawia się w:
    Annales Societatis Geologorum Poloniae
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Epigenetic silicification of the Upper Oxfordian limestones in the Sokole Hills (Kraków-Częstochowa Upland): relationship to facies development and tectonics
    Autorzy:
    Matyszkiewicz, J.
    Kochman, A.
    Rzepa, G.
    Gołębiowska, B.
    Krajewski, M.
    Gaidzik, K.
    Żaba, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/138902.pdf
    Data publikacji:
    2015
    Wydawca:
    Polska Akademia Nauk. Czytelnia Czasopism PAN
    Tematy:
    Upper Jurassic limestones
    epigenetic silicification
    tectonic deformations
    Kraków-Częstochowa Upland
    wapienie górnej jury
    deformacje tektoniczne
    Wyżyna Krakowsko-Częstochowska
    Opis:
    A spectacular epigenetic silicification was encountered in the Oxfordian bedded limestones exposed in the Sokole Hills situated in the Kraków-Częstochowa Upland. The main epigenetic mineral is microcrystalline quartz accompanied by minor goethite, hematite, barite, galena and sphalerite. Locally, the mineralized limestones reveal Pb and Cu contents exceeding over 150 times the background values of these metals in unmineralized limestones. The epigenetic mineralization of the bedded limestones was probably a two-stage process. During the first, Early Cretaceous stage, silicified limestones formed at the erosional surface of a denuded carbonate complex. Such silicification greatly limited the progress of the first karstification phase of the Upper Jurassic carbonates initiated in the Hauterivian. The sources of silica accumulated in the limestones were descending solutions enriched in silica derived from the weathering zone. This silicification affected the topmost part of the Upper Jurassic massive limestones and the deeper portions of the bedded limestones along the fracture systems and stylolites. Early Cretaceous tectonic activity generated new dislocations and re-opened the existing faults, which were subsequently filled with permeable Albian quartz sands. These openings became the migration pathways for ascending, warm, relict, sulphide-carrying hydrothermal solutions at the second formation stage of the epigenetic mineralization. The newly supplied silica from the Albian sands precipitated on the silicified limestones and, as concentric rims, on brecciated, early diagenetic cherts. The second-stage mineralization proceeded under phreatic conditions, presumably close to a fluctuating mixing zone of ascending, warm hydrothermal solutions and descending cold groundwaters. The brecciated cherts acting as silica crystallization nuclei indicate that the last mineralization stage probably followed the final phase of Cenozoic faulting.
    Źródło:
    Acta Geologica Polonica; 2015, 65, 2; 181-203
    0001-5709
    Pojawia się w:
    Acta Geologica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-8 z 8

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