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    Wyświetlanie 1-5 z 5
    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:
    Gold recovery from refractory gold concentrates by pressure oxidation pre-treatment and thiosulfate leaching
    Autorzy:
    Yu, Li
    Li, Shimei
    Liu, Quanjun
    Deng, Jiushuai
    Luo, Bin
    Liang, Yuanqin
    Zhao, Liuchuang
    Lai, Hao
    Powiązania:
    https://bibliotekanauki.pl/articles/110871.pdf
    Data publikacji:
    2019
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    gold
    pressure oxidation
    thiosulfate
    leaching
    RSM
    Opis:
    Naturally, refractory gold is enclosed by sulfide minerals such as pyrite and arsenopyrite and a higher content of organic carbon, which results in difficulty in the recovery of gold. In this study, the flotation gold concentrate before and after pressure oxidation (POX) was analyzed. The analysis of the Eh-pH diagram revealed that pyrite/arsenopyrite would be dissolved in higher oxidation potential. Results of SEM-EDS showed that the surface of minerals became very rough and structure of some particles was destroyed after POX. The XRD measurement showed that pyrite was oxidized to jarosite, and gangue minerals such as quartz and organic carbon were hardly changed. The process of thiosulfate leaching of gold was designed and optimized according to Miscellaneous implemented by Response Surface Methodology (RSM). Based on the results of ANOVA, leaching model was significant. In leaching, [S2O32-] played an important role and the interactions between [S2O32-] and [Cu2+] were significant. The effect of [HA] was relatively weak. Optimum process parameters of the initial reagent concentration were 505.00 mM for [S2O32-], 34.77 mM for [Cu2+], and 0.50 mM for [HA]. Under these conditions, the Au extraction value was about 86.21%, which was significantly higher than that obtained with leaching directly.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2019, 55, 2; 537-551
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Activation mechanism of tantalum niobium flotation by lead ions in a combined collector flotation system
    Autorzy:
    He, Mingfei
    Li, Shuangke
    Cao, Miao
    Gao, Yude
    Bu, Hao
    Meng, Qingbo
    Powiązania:
    https://bibliotekanauki.pl/articles/1448361.pdf
    Data publikacji:
    2021
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    tantalum niobium ore
    Pb2+ ions activation
    ammonium dibutyl dithiophosphate
    coadsorption
    Opis:
    The effect of lead ions on the flotation activation of tantalum niobium ore (TNO) was studied by micro-flotation, adsorption capacity experiments, solution chemical composition calculations, and infrared spectral analysis. The experimental demonstrated that the combined collector of salicylhydroxamic acid (SHA) and ammonium dibutyl dithiophosphate (ADDP) resulted in a strong collection capacity for TNO in the presence of lead ions. The solution chemistry calculations determined that the dominant source of lead ions in the aqueous solution was $Pb(OH)^+$ at a pH of 8, which was conducive to the adsorption and interaction of SHA and ADDP anions. In the lead ion activation system, the combined reagent co-adsorbed onto the TNO surface, causing a large negative shift in the zeta potential. The co-adsorption mechanism of the combined collector consisted of complex chemisorption between SHA and the TNO surface active particles, while the main adsorption of ADDP is physisorption.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2021, 57, 1; 29-38
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Effect of the degree of polymerization of nonylphenol polyoxyethylene ether on the dewatering of low-rank coal
    Autorzy:
    Li, Lin
    He, Meng
    Liu, Mingpu
    Lin, Mengyu
    Hu, Shanpei
    Yu, Hao
    Wang, Qingbiao
    You, Xiaofang
    Powiązania:
    https://bibliotekanauki.pl/articles/1449205.pdf
    Data publikacji:
    2020
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    low-rank coal
    NPEO
    dewatering
    adsorption
    long-flame coal
    Opis:
    In this study, we investigated the effect of the hydrophilic ethylene oxide chain lengths (i.e., degree of polymerization) of nonylphenol polyoxyethylene ether (NPEO-x, x = 8, 10, and 12) on the dewatering of low-rank coal slime through dewatering and adsorption experiments and X-ray photoelectron spectroscopy (XPS) measurements. The dewatering experiments showed that the adsorption of NPEO changed the water content of the low-rank coal slime: NPEO-8 achieved the best effect, followed, in decreasing order, by NPEO-10 and NPEO-12. Adsorption experiments revealed that the adsorption isotherms of NPEO-x on the low-rank coal surface conform with the Langmuir model, and its adsorption kinetics follow the pseudo-second-order kinetic equation. Furthermore, the adsorption is a spontaneous process and controlled by both intraparticle diffusion and liquid film diffusion. The XPS results showed that the adsorption of NPEO-x decreased the content of oxygencontaining groups and, thus, improved the hydrophobicity of the low-rank coal surface. Further, the use of NPEO-x with a low degree of polymerization (x = 8) improves the hydrophobicity of the coal surface and decreases the water content of low-rank coal slime.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2020, 56, 4; 723-736
    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 1-5 z 5

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