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Wyszukujesz frazę "cerussite" wg kryterium: Temat

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    Wyświetlanie 1-6 z 6
    Tytuł:
    Evaluation of ammonium citrate tribasic as a leaching reagent for lead-bearing ore
    Autorzy:
    Liu, Junbo
    Li, Shimei
    Zhao, Biao
    Deng, Jianying
    Huang, Lingyun
    Zhou, Yuanyuan
    Chen, Cong
    Liu, Quanjun
    Powiązania:
    https://bibliotekanauki.pl/articles/109649.pdf
    Data publikacji:
    2019
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    lead
    cerussite
    ammonium citrate tribasic
    leaching
    kinetics
    Opis:
    In this study, the leaching process of a lead-bearing ore, consisting mainly of cerussite, in an ammonium citrate tribasic medium was investigated. The parameters including temperature, reagent concentration, particle size, and stirring speed were examined. During leaching process, the lead conversion rate increased with an increase in reagent concentration, reaction temperature, and stirring speed, and a decrease in particle size. The results show that about 95% of lead content was extracted from the samples with particle size range of +75-96 μm after 21 min leaching in 1.25 mol/L ammonium citrate tribasic solution at 800 r/min and 40°C. It was found that the leaching reaction followed the shrinking core model. The results indicated that ammonium citrate tribasic could be used as an effective leaching reagent for extracting lead from lead oxide ore.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2019, 55, 3; 689-700
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Investigation of leaching kinetics of cerussite in sodium hydroxide solutions
    Autorzy:
    Feng, Q.
    Wen, S.
    Wang, Y.
    Zhao, W.
    Deng, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/110621.pdf
    Data publikacji:
    2015
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    cerussite
    sodium hydroxide
    leaching
    kinetics
    activation energy
    Opis:
    The leaching kinetics of cerussite in alkaline medium was investigated with respect to experimental variables such as sodium hydroxide concentration, temperature, particle size and stirring speed. The results showed that leaching reagent concentration and reaction temperature exerted significant effects on the extraction of lead, whereas particle size and stirring speed exhibited a relatively moderate effect on the leaching rate. The leaching process followed the kinetic law of the shrinking core model, and the dissolution rates were controlled by the surface chemical reaction with an apparent activation energy value of 43.79 kJ/mol. A corresponding dissolution kinetic equation was also proposed to describe the dissolution reaction. The results indicated that sodium hydroxide could be used as an effective leaching reagent for extracting lead from cerussite.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2015, 51, 2; 491-500
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Study on surface modification of cerussite by thermochemical processing with pyrite
    Autorzy:
    Zheng, Yong-Xing
    Ning, Ji-Lai
    Xie, Haiyun
    Lv, Jin-Fang
    Hu, Pan-Jin
    Pang, Jie
    Powiązania:
    https://bibliotekanauki.pl/articles/1448573.pdf
    Data publikacji:
    2021
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    cerussite
    pyrite
    surface modification
    thermochemical processing
    flotation
    Opis:
    In this paper, surface modification of cerussite by thermochemical processing with pyrite was studied based on microflotation tests, X-ray powder diffractometry (XRD), X-ray photoelectron spectroscopy (XPS) and electron probe microanalysis (EPMA). Microflotation test results showed that the surface modification facilitated flotation of the treated cerussite and improved the flotation recovery to approximately 90%. The results of XRD analyses confirmed that cerussite was transformed into massicot, which then interacted with pyrite to form $PbS$, $PbSO_4$, $PbO•PbSO_4$ and $4PbO•PbSO_4$. XPS analyses results revealed that both $PbS$ and $PbS_2$ were formed on the mineral surface, and the percentage of $PbS$ increased with increasing $FeS_2$/$PbCO_3$ (F/P) mole ratio, which was advantageous for the flotation of the modified cerussite. EPMA analyses showed that particles with layered configurations were obviously formed after thermochemical processing. The thickness of the products at the outer layer of the particles increased when the F/P mole ratio increased. Moreover, the S and O contents in the products increased and decreased, respectively.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2021, 57, 1; 156-167
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Effect of pH on surface characteristics and flotation of sulfidized cerussite
    Autorzy:
    Feng, Q.
    Wen, S.
    Zhao, W.
    Liu, J.
    Liu, D.
    Powiązania:
    https://bibliotekanauki.pl/articles/110234.pdf
    Data publikacji:
    2016
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    cerussite
    sulfidization
    excessive sulfide ions
    pH
    surface analysis
    Opis:
    The effect of pH on surface characteristic and flotation of sulfidized cerussite was studied by micro-flotation tests, dissolution experiments, scanning electron microscopy (SEM) energy dispersive spectrometer (EDS), and X-ray photoelectron spectroscopy (XPS). The micro-flotation tests demonstrated that higher recovery of cerussite was achieved in acidic solutions than that in alkaline solutions. Despite the addition of high collector concentrations, cerussite flotation did not improved in alkaline solutions. The dissolution performance of sulfide-treated cerussite at different pH values indicated that the lead sulfide layer on the surface of sulfide-treated cerussite could exist in acidic solutions and it was more stable at acidic pH than in alkaline solutions. This finding was proved by the SEM-EDS and XPS analyses.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2016, 52, 2; 676-689
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Remarks on the origin of cerussite in the Upper Silesian Zn-Pb deposits, Poland
    Autorzy:
    Szczerba, Marek
    Sawłowicz, Zbigniew
    Powiązania:
    https://bibliotekanauki.pl/articles/2086512.pdf
    Data publikacji:
    2009
    Wydawca:
    Polskie Towarzystwo Mineralogiczne
    Tematy:
    Zn-Pb deposits
    Upper Silesia
    cerussite
    oxidation
    galvanic coupling
    Opis:
    Cerussite, the most important oxidized lead mineral in the Upper Silesian Zn-Pb deposits, occurs in two readily distinct types: fine-grained cerussite replacing galena in-situ and macrocrystalline cerussite filling open fractures and cavities. Microscopic observations and thermodynamic considerations lead to the conclusion that galena can be oxidized to lead carbonate directly, not necessarily through an intermediate sulphate phase. Locally present iron sulphides undergoing oxidation acidify solutions and provide ferric ions which are important oxidizing agents. In such microenvironments, anglesite can preferentially form. Cerussite and galena commonly coexist together with non-oxidized zinc sulphides. It is difficult to explain such assemblages if galvanic couplings made of these two sulphides are not considered. These couplings are only formed when these two sulphides are in direct contact. In such an assemblage, galena undergoes oxidation, mostly to cerussite, and sphalerite is passivated. When there is no direct contact between sulphides, the galvanic couplings do not exist. Galena surfaces become covered by oxidation products which inhibit further oxidation. As such a cover does not form on sphalerite, it can be easily oxidized.
    Źródło:
    Mineralogia; 2009, 40, 1/4; 53--64
    1899-8291
    1899-8526
    Pojawia się w:
    Mineralogia
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Remarks on the origin of cerussite in the Upper Silesian Zn-Pb deposits, Poland
    Autorzy:
    Szczerba, M.
    Sawłowicz, Z.
    Powiązania:
    https://bibliotekanauki.pl/articles/2086558.pdf
    Data publikacji:
    2009
    Wydawca:
    Polskie Towarzystwo Mineralogiczne
    Tematy:
    Zn-Pb deposits
    Upper Silesia
    cerussite
    oxidation
    galvanic coupling
    Opis:
    Cerussite, the most important oxidized lead mineral in the Upper Silesian Zn-Pb deposits, occurs in two readily distinct types: fine-grained cerussite replacing galena in-situ and macrocrystalline cerussite filling open fractures and cavities. Microscopic observations and thermodynamic considerations lead to the conclusion that galena can be oxidized to lead carbonate directly, not necessarily through an intermediate sulphate phase. Locally present iron sulphides undergoing oxidation acidify solutions and provide ferric ions which are important oxidizing agents. In such microenvironments, anglesite can preferentially form. Cerussite and galena commonly coexist together with non-oxidized zinc sulphides. It is difficult to explain such assemblages if galvanic couplings made of these two sulphides are not considered. These couplings are only formed when these two sulphides are in direct contact. In such an assemblage, galena undergoes oxidation, mostly to cerussite, and sphalerite is passivated. When there is no direct contact between sulphides, the galvanic couplings do not exist. Galena surfaces become covered by oxidation products which inhibit further oxidation. As such a cover does not form on sphalerite, it can be easily oxidized.
    Źródło:
    Mineralogia; 2009, 40, 1/4; 53--64
    1899-8291
    1899-8526
    Pojawia się w:
    Mineralogia
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-6 z 6

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