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Wyświetlanie 1-4 z 4
Tytuł:
The Rietveld refinement studies of pyromorphite-vanadinite and mimetite-vanadinite solid solution series
Autorzy:
Solecka, U.
Zelek, S.
Bajda, T.
Powiązania:
https://bibliotekanauki.pl/articles/184341.pdf
Data publikacji:
2016
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Wydawnictwo AGH
Tematy:
apatite supergroup
oxidation zone
ore deposit
Opis:
Mimetite Pb 5 (PO 4 ) 3 Cl, vanadinite Pb 5 (VO 4 ) 3 Cl and pyromorphite Pb 5 (PO 4 ) 3 Cl belong to the apatite supergroup. They form in oxidation zones of lead ore deposits. These minerals have high thermal stability (Dong et al. 2002) and low solubility (Flis et al. 2011) thus they have many applications. Pyromorphite and mimetite are especially used to immobilize lead in contaminated soils and hazardous industrial wastes (Ma et al. 1993, Kim et al. 2005, Bajda et al. 2007), it is therefore important to know the impact of various factors on their properties. Crystal structure of apatites corresponds to the general formula M 5 (TO 4 ) 3 X, where M are bi - valent cations distributed on two distinct crystallographic sites, TO 4 is a trivalent oxyanion and X is a monovalent anion. The structure and chemistry of apatite allow for numerous substitutions of metal cation and anionic complexes (Hughes & Rakovan 2002, Pan & Fleet 2002). It was found that substitutions cause variations in the unit cell parameters and chemical properties of these minerals (Botto et al. 1997), but there are no articles presenting variations in the whole series. Therefore, these researches present changes of lattice parameters for pyromorphite-vanadinite and mimetite-vanadinite solid solution series. Pyromorphite, mimetite and vanadinite crystallize in hexagonal symmetry (the space group P6 3 /m) (Dong et al. 2002, Pan & Fleet 2002). They form continuous isomorphic series. The aim of study was to examine how lattice parameters of pyromorphite-vanadinite and mimetite-vanadinite solid solutions series change with increasing vanadium content and characterize these pheno mena. Crystallographic studies were conducted on synthetic pyromorphite, mimetite and vanadinite and minerals with intermediate compositions Pb 5 (TO 4 ) 3 Cl, where T = P + V or As + V, of various P/V or As/V ratios. Samples were analyzed by X-Ray diffraction (XRD) using RIGAKU Smartlab X-Ray diffractometer with Cu radiation in a 10° to 110° 2Θ range at a step size of 0.02 2Θ and a rate of 2 s per step. The phase identification was carried out using the X’Rayan computer program and X-ray standard patterns in the form of ICDD files (card 19-0701, 19-0683 and 43-1461). The unit-cell refinement and Rietveld structure refinement were made using the FullProf Suite computer program package (Rodriguez-Carvajal 1993). The Rietveld refinement has shown systematic changes in unit cell parameters of studied samples depending on their chemical composition. Dimensions of unit cell parameters of pyromorphite-vanadinite solid solution series increase linearly with the substitution of vanadate ions in the structure of pyromorphite. Lattice parameter “a” increase in the range of 9.987–10.325 Å, while lattice parameter “c” increase in the range of 7.33–7.343 Å. In case of the mimetite-vanadinite solid solution series, lattice parameter “a” increase (10.251–10.325 Å range), whereas lattice parameter “c” decrease (7.442–7.343 Å range) linearly with the substitution of vanadate ions in the structure of mimetite. This situation indicates the equivalent position of the tetrahedral TO 4 in the structure of lead apatite.
Źródło:
Geology, Geophysics and Environment; 2016, 42, 1; 127-128
2299-8004
2353-0790
Pojawia się w:
Geology, Geophysics and Environment
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The philipsbornite–segnitite solid-solution series from Rędziny, eastern metamorphic cover of the Karkonosze granite (SW Poland)
Autorzy:
Gołębiowska, B.
Włodek, A.
Pieczka, A.
Borkiewicz, O.
Polak, M.
Powiązania:
https://bibliotekanauki.pl/articles/191534.pdf
Data publikacji:
2016
Wydawca:
Polskie Towarzystwo Geologiczne
Tematy:
arsenates
oxidation zone
philipsbornite
segnitite
carminite
chemical composition
Rędziny
Opis:
Supergene minerals of the philipsbornite–segnitite series, PbAl3(AsO4)(AsO3OH)(OH)6–PbFe3+3(AsO4) (AsO3OH)(OH)6, accompanied by carminite, PbFe3+2(AsO4)2(OH)2, were found in relics of hydrothermal quartz– chlorite–arsenopyrite veins, associated with subordinate polymetallic ores disseminated in contact zones of a dolomitic marble deposit at Rędziny, Western Sudetes, Poland, and recognized by means of electron microprobe and X-ray and electron-back-scattered diffraction (XRD and EBSD). Philipsbornite and segnitite, as the two minerals of the series, exhibit highly variable compositions, especially in terms of the range of Fe3+ Al3+ substitution at the G site, with a distinct gap between the values of 0.52 and 0.89 for the Fe/(Al+Fe) ratio; substitutions at the D and T sites are less important. In this respect, the minerals are almost identical with philipsbornite and segnitite, known from other localities. The gap might be a consequence of the limited miscibility of the end-members, but also might be attributed to crystallization under the changing and distinctly differing activities of Al3+ and Fe3+. The unit-cell parameters of philipsbornite, a = 7.1245(13) Ο, c = 17.0967(45) Ο, make the mineral comparable with philipsbornites from other occurrences. The EBSD analysis confirmed the rhombohedral structure of both minerals and the space group symmetry R-3m. The minerals crystallized in the sequence: philipsbornite -> segnitite -> carminite, which reflects (i) decreasing acidity in the oxidation zone, due to the leaching of sulphate ions and interaction of the solutions with a nearby dolomite lens, and (ii) varying activities of Al3+, Fe3+ and Pb2+ cations, mobilized by the solutions through interaction with the silicate host containing disseminated arsenopyrite and subordinate sulphides, up to complete Pb2+ depletion.
Źródło:
Annales Societatis Geologorum Poloniae; 2016, 86, 1; 73-83
0208-9068
Pojawia się w:
Annales Societatis Geologorum Poloniae
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Recently formed arsenates from an abandoned mine in Radzimowice (SW Poland) and the conditions of their formation
Autorzy:
Siuda, Rafał
Januszewska, Anna
Powiązania:
https://bibliotekanauki.pl/articles/24024699.pdf
Data publikacji:
2022
Wydawca:
Polska Akademia Nauk. Czasopisma i Monografie PAN
Tematy:
Bukovskyite
kaňkite
zýkaite
pitticite
iron arsenates
oxidation zone
Radzimowice
bukowskit
kankit
zykait
pitticit
arseniany
żelazo
strefa aeracji
minerały wtórne
Opis:
In the mining galleries of the abandoned Au-As mine in Radzimowice, diverse groups of secondary arsenates crystallized recently. They form several characteristic assemblages. In the first of them the typical minerals are bukovskýite and melanterite. The second group of secondary arsenates includes scorodite, kaňkite, zýkaite, and pitticite. The third assemblage includes Co-Ni-Mg arsenates of the erythrite-annabergite-hörnesite series. The first assemblage crystallized in a zone with a very high activity of sulphate and arsenate ions and where the pH varies within a narrow range of 2.0-3.5. The second group of secondary arsenates formed in the acidic zone. The minerals identified here suggest pH variation within fairly wide ranges, from about 2.0 to 5.5. Contrary to the first and second mineral assemblage, the Co-Ni-Mg arsenates formed under different geochemical conditions. Their crystallization took place under weak acidic to neutral conditions.
Źródło:
Acta Geologica Polonica; 2022, 72, 4; 423--442
0001-5709
Pojawia się w:
Acta Geologica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Badania stanu powierzchni elementu poddanego tarciu w oleju bazowym metodą potencjometryczną
Research of the element surface exposed to friction in the base oil by potentiometry
Autorzy:
Kosmynina, M.
Bukalska, E.
Michalak, P.
Powiązania:
https://bibliotekanauki.pl/articles/189154.pdf
Data publikacji:
2012
Wydawca:
Stowarzyszenie Inżynierów i Techników Mechaników Polskich
Tematy:
aktywność metali
hydrorafinat
potencjał elektryczny
stopień utlenienia
strefa tarcia
active metals
electric potential
degree of oxidation
zone of friction
Opis:
W urządzeniach mechanicznych zabezpieczenie antykorozyjne oraz wymagane właściwości tribologiczne elementów wykonanych ze stali uzyskiwane są poprzez zanurzenie w środowisku dielektrycznym lub nałożenie warstwy smarowej. W pracy omówiono aktywność stali C45 z elektrolitycznie osadzonymi powłokami w środowisku o właściwościach dielektrycznych (hydrorafinacie II). Wykładnikiem aktywności tworzywa metalicznego jest napięcie elektryczne mierzone względem elektrody porównawczej. Podczas współpracy elementów uaktywnia się część powierzchni poddanej procesowi tarcia. Dla dwóch współpracujących pierścieni jest to obszar ich powierzchni bocznej. Pozostała powierzchnia pierścienia wykazuje potencjał wyjściowy. Wstępnie utleniona powierzchnia powłoki podczas procesu tribologicznego jest usuwana i odkrywa rdzeń powłoki. Uaktywnienie rdzenia powłoki pozwala na konstytuowanie procesów chemicznych (wymiany) i elektrochemicznych.
The protection of corrosion in mechanical devices and tribological properties of steel components, which are required, is achieved either through the immersion in the dielectric environment or through applying a grease layer. The activity of C45 steel with electrolytically embedded coatings in the environment of dielectric properties (hydrorafinat II) is described in this work. The exponent of the metal material activity is the electric voltage, which is measured relative to the reference electrode. During the cooperation of the elements, the activated surface is subjected to the process of friction. For the two rings, this is the area of their lateral surface. The rest of the surface of the ring has initial potential. During the tribological process, the oxidised surface of the coating is removed revealing its core. The process of the activation of the core of the coating allows the creation of the chemical processes (exchange) and electrochemical processes.
Źródło:
Tribologia; 2012, 3; 77-84
0208-7774
Pojawia się w:
Tribologia
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

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