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    Wyświetlanie 1-3 z 3
    Tytuł:
    Basic theory and optimization of gold containing antimony concentrate leaching by alkaline sulfide
    Autorzy:
    Wu, Hao
    Feng, Yali
    Li, Haoran
    Liao, Shengde
    Wang, Hongjun
    Powiązania:
    https://bibliotekanauki.pl/articles/109524.pdf
    Data publikacji:
    2019
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    antimony concentrate
    leaching process
    alkaline leaching
    kinetics
    Opis:
    As sodium sulfide is easily oxidized to polysulfide and thiosulfate which have a gold leaching effect, gold would dissolve in leaching solution when extracting stibium from gold containing antimony concentrate by alkaline sulfide. Through leaching test and kinetics analysis, the decomposition regularity of sodium sulfide and leaching rate were studied under different leaching conditions. The results indicated that the gold content in antimony concentrate was 28.41g/Mg, and the content of antimony and sulfur was 36.01% and 14.04%, respectively. The main metallic minerals were native gold, arsenopyrite, stibnite, and the gangue minerals were mainly quartz. Anodic polarization curve shows reduced iron powder can increase the peak potential of the oxidation of the leaching solution and it can effectively prevent the decomposition of sodium sulfide and the dissolution of gold. Optimized stibium-extraction efficiency was achieved under the following conditions: a concentration of sodium sulfide and sodium hydroxide at 110g/dm³ and 20g/dm³, respectively; a ratio of iron powder to concentrate of 1:30; a ratio of liquid to solid of 5:1; agitation speed of 600rad/min; reaction temperature of 353.15K; and a reaction time of 3 h. Under the optimized conditions, high antimony recovery (97.35%) and low gold dissolution (1.32%) were achieved.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2019, 55, 1; 248-257
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Investigating the selectivity of calcium hypochlorite for flotation separation of chalcopyrite and pyrite pre-adsorbed collector
    Autorzy:
    Yang, Wenhui
    Qiu, Xianhui
    Yan, Huashan
    Wu, Hao
    Yang, Liu
    Lai, Ruisen
    Qiu, Tingsheng
    Powiązania:
    https://bibliotekanauki.pl/articles/2146919.pdf
    Data publikacji:
    2022
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    pyrite
    chalcopyrite
    calcium hypochlorite
    flotation separation
    Opis:
    Bulk flotation is usually used in the flotation of Cu-Fe sulfide ore, and the subsequent concentrate is difficult to be separated because the minerals have adsorbed the collector. In this paper, flotation tests showed that calcium hypochlorite (Ca(ClO)2) had a stronger depression effect on pyrite pre-adsorbed sodium butyl xanthate (SBX), while having a negligible depressive effect on chalcopyrite. A copper concentrate with Cu grade of 33.32% and Cu recovery of 94.47% could be obtained from flotation tests of mixed minerals. The depression performance and mechanism of Ca(ClO)2 were studied by contact angle measurements, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses, the results suggested that Ca(ClO)2 can decomposes SBX on the pyrite surface and oxidizes the mineral surface to form hydrophilic substances, which enhances the hydrophilicity of the pyrite surface. In contrast, Ca(ClO)2 has little effect on chalcopyrite pre-adsorbed SBX, the possible depression model is discussed.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2022, 58, 4; art. no. 150703
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Adsorption of hydrated Fe(OH)2+ on the kaolinite surface: A density functional theory study
    Autorzy:
    Wu, Hongqiang
    Miao, Yuqi
    Long, Qibang
    Yan, Huashan
    Li, Yong
    Qiu, Sen
    Wu, Hao
    Zhao, Guanfei
    Qiu, Tingsheng
    Powiązania:
    https://bibliotekanauki.pl/articles/27323639.pdf
    Data publikacji:
    2023
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    kaolinite
    adsorption
    Fe
    density functional theory
    Opis:
    The present study employed density functional theory (DFT) to analyze the adsorption configuration and mechanism of Fe(OH)2+ on the kaolinite (001) surface. The findings demonstrated that Fe(OH)2(H2O)4+ is the main type in which hydrated Fe(OH)2+ can be found in aqueous solution. On the surface of kaolinite, Fe(OH)2(H2O)4+ will be adsorbed. There are two forms of adsorption: outer-sphere and inner-sphere coordination (monodentate/bidentate) adsorption. Fe(OH)2(H2O)4+ has a moderate propensity to adsorb on the alumina octahedral sheet of kaolinite when the outer-sphere coordination adsorption takes place. In cases of inner-sphere coordination adsorption, Fe exhibits a tendency to form monodentate adsorption compounds in conjunction with Ou atoms. Additionally, it prefers to create bidentate adsorption compounds through coordination with both Ot and Ou atoms. The adsorption mechanism analysis results show that the ionic property of Fe atom decreases after outer-sphere coordination adsorption. After inner-sphere coordination adsorption, some electrons of Fe atom are transferred to the surface O atom. The presence of electrons between the Fe and O atoms enhances the formation of bonds, hence enhancing the covalent nature of the Fe-O bond. Theoretical FT-IR (Fourier transform infrared spectroscopy) calculations show that the formation of Fe-O chemical bonds. Because of the lower adsorption energy and more chemical bonds, hydrate Fe(OH)2+ is more likely to be bidentate adsorbed on the kaolinite surface.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2023, 59, 6; art. no. 174415
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-3 z 3

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