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Tytuł:
Effect of pyrite type on the electrochemistry of chalcopyrite/pyrite interactions
Autorzy:
Forbes, E.
Smith, L.
Vepsalainen, M.
Powiązania:
https://bibliotekanauki.pl/articles/110218.pdf
Data publikacji:
2018
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
flotation
arsenic
pyrite
galvanic interaction
Surface oxidation
Opis:
Pyrite is the most common sulphide gangue mineral occurring in base metal sulphide ores around the world. Pyrite is known to galvanically interact with valuable minerals such as chalcopyrite, altering their electrochemical and flotation behaviour. Different types of pyrite are known to vary in texture, chemical composition and electrochemical activity. However, the effect that these differences have on the degree of pyrite interaction with chalcopyrite are not well studied. This work examines two distinct types of pyrite from different deposits that have a similar chemical composition, but vary greatly in texture. It investigates the way in which these pyrites interact with chalcopyrite surfaces, affecting both its electrochemical behaviour and floatability. It was found that the Renison pyrite was characterised by a much higher level of surface activity than the Huanzala pyrite. This was attributed to the elevated levels of arsenic within the mineral’s crystalline matrix.
Źródło:
Physicochemical Problems of Mineral Processing; 2018, 54, 4; 1117-1129
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mechanism and kinetics of pyrite transformation at elevated temperatures
Autorzy:
Aracena, Alvaro
Jerez, Oscar
Powiązania:
https://bibliotekanauki.pl/articles/2146885.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
pyrite
pyrrhotite
roasting
kinetics
Opis:
Pyrite (FeS2) is known as a sulfide that provides energy for various pyrometallurgical processes (fusion and conversion). There are several studies related to the evaluation of pyrite oxidation mechanisms at high temperatures, obtaining discrepancies in the products generated. In our work, the novelty of our research would be to obtain the thermochemical oxidation mechanism of FeS2 by using conventional thermogravimetric methods. The oxidative roasting of pyrite from 550 to 800°C was analyzed for an oxygen concentration of 5.07 to 28.06 kPa of oxygen and particle size between 12.3 to 33.8 microns. The results showed that the pyrite proceeded by sequential roasting: first, it produced an intermediate compound, pyrrhotite (Fe7S8), which was later oxidized to generate hematite (Fe2O3), both stages validated by weight loss of the sample as well as by analysis by DRX. Each stage had a different roasting speed as it was also influenced differently by different parameters. The temperature and particle size favored the rate of pyrrhotite generation, and the oxygen concentration favored the rate of hematite formation. The first-order kinetic equation ln (1-XPy) represented the roasting of the first stage (FeS2 → Fe7S8), with a calculated activation energy of 70.1 kJ/mol. The order of reaction was 0.5 concerning the partial pressure of oxygen and inversely proportional to the initial particle radius.
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 6; 127--139
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Chlorinated benzenes and benzene degradation in aerobic pyrite suspension
Autorzy:
Pham, Hoa Thi
Chihiro, Inoue
Powiązania:
https://bibliotekanauki.pl/articles/205353.pdf
Data publikacji:
2019
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
benzene
degradation
pyrite
aerobic
chlorinated benzene
Opis:
The focus of this study is to investigate the applicability of natural mineral iron disulfide (pyrite) in degradation of aromatic compounds including benzene and several chlorinated benzenes (from mono-chlorinated benzene (CB), di-chlorinated benzenes (di-CBs) to tri-chlorobenzenes (tri-CBs) in aerobic pyrite suspension by using laboratory batch experiments at 25°C and room pressure. At first, chlorobenzene was studied as a model compound for all considered aromatic compounds. CB was degraded in aerobic pyrite suspension, transformed to several organic acids and finally to CO2 and Clˉ. Transformations of remaining aromatic compounds were pursued by measuring their degradation rates and CO2 and Clˉ released with time. Transformation kinetics was fitted to the pseudo-first-order reactions to calculate degradation rate constant of each compound. Degradation rates of the aromatic compounds were different depending on their chemical structures, specifically the number and position of chlorine substituents on the benzene ring in this study. Compounds with the highest number of chlorine substituent at m-positions have highest degradation rate (1,3,5-triCB > 1,3-diCB > others). Three chlorine substituents closed together (1,2,3-triCB) generated steric hindrance effects. Therefore 1,2,3-triCB was the least degraded compound The degradation rates of all compounds were in the following order: 1,3,5-triCB > 1,3-diCB > 1,2,4-triCB ≅1,2-diCB ≅CB ≅benzene > 1,4-diCB > 1,2,3-triCB. The final products of the transformations were CO2 and Clˉ. Oxygen was the common oxidant for pyrite and aromatic compounds. The presence of aromatic compounds reduced the oxidation rate of pyrite, which reduced the amount of ferrous and sulfate ions release to aqueous solution.
Źródło:
Archives of Environmental Protection; 2019, 45, 1; 115-125
2083-4772
2083-4810
Pojawia się w:
Archives of Environmental Protection
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The influence of cyanide salts and ferrous sulphate on pyrite flotation
Autorzy:
Kostovic, M.
Vucinic, D.
Powiązania:
https://bibliotekanauki.pl/articles/110668.pdf
Data publikacji:
2016
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
pyrite
flotation
ferrous sulphate
cyanide salts
depression
Opis:
The effect of cyanide salts as depressants, i.e. sodium cyanide (NaCN) and complex cyanide salts such as potassium ferricyanide (K3Fe(CN)6) and potassium ferrocyanide (K4Fe(CN)6), as well as combination of sodium cyanide with ferrous sulphate (FeSO4/NaCN) on pyrite flotation was investigated. Tests covered the frothless flotation of pyrite under different concentrations of depressants at various solution pH’s with potassium butyl xanthate (KBX) as collector. Flotation test results have shown that NaCN, and even more the combination of reagents FeSO4/NaCN are more successful in pyrite depression than complex cyanide salts, such as K3Fe(CN)6 and K4Fe(CN)6. Surface characteristics of pyrite were studied using rest potential (Eh) measurements and infrared attenuated total reflection spectroscopy (ATR-IR). In the presence of tested reagents in the flotation system, iron cyanide compounds and hydrated iron oxides were formed on pyrite surface. The composition of formed compounds depends not only on cyanide ions in the solution, but also on the pH of the system and solution species. These compounds, depending on the reagents used, are responsible for the resulting efficiency of the pyrite depression.
Źródło:
Physicochemical Problems of Mineral Processing; 2016, 52, 2; 609-619
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Flotation separation influenced by the rheological properties of diaspore-pyrite mixed pulp
Autorzy:
Zhao, Yongqing
Li, Xianhai
Powiązania:
https://bibliotekanauki.pl/articles/27323666.pdf
Data publikacji:
2023
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
bauxite
diaspore
pyrite
flotation
rheological property
viscosity
Opis:
The effects of pyrite and diaspore with different particle sizes on the rheological properties of pulp with butyl xanthate added as a collector were studied, and the mechanism for rheological pyrite separation from diaspore by flotation was probed. The apparent viscosity of the diaspore pulp with different particle sizes was higher than that of pyrite, especially for -30 μm diaspore. Microfine diaspore was an important component affecting the apparent viscosity and yield stress of the diaspore-pyrite mixed pulp, and the pulp became a non-Newtonian fluid when the mass fraction of fine-grained diaspore in the mixed pulp was high. In this study, sodium hexametaphosphate (SHMP) was used to control the rheology of the mixed pulp and improve the pyrite flotation, and the S (sulfur) recovery rate first increased and then decreased with increasing SHMP concentration. The apparent viscosity of the pulp decreased by 3.01% and the S recovery rate increased by 34.83% when the amount of added SHMP was 0.05 mg/kg. The apparent viscosity with 0.50 mg/kg SHMP was 21.76% lower than that seen with the addition of 0.05 mg/kg SHMP, but the S recovery rate was also reduced by 14.94%. Further research showed that the increased SHMP concentration led to increases in the electronegativities of the particle surface and the repulsive force between particles, which prevented agglomeration of the particles, reduced the apparent viscosity and yield stress of the mixed pulp, promoted collisions between the pyrite particles and the bubbles, and reduced the resistance of the air bubbles to flotation.
Źródło:
Physicochemical Problems of Mineral Processing; 2023, 59, 6; art. no. 174305
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparison of anionic, cationic and amphoteric collectors used in pyrite flotation
Autorzy:
Bulut, Gülay
Sirkeci, A. A.
Arı, Beril
Powiązania:
https://bibliotekanauki.pl/articles/1446764.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
flotation
pyrite
amine
collectors
xanthate
Opis:
In this study, flotation tests were conducted with purified pyrite and ore samples. The collectors employed were anionic and cationic type such as potassium ethlyl-amyl xanthate, Tomamine M73 and Resanol Bal. According to the flotation tests, it was found that pyrite floated at low pH and depressed at high pH values with xanthates. On the other hand, in the case of cationic collectors which are Tomamine M73 (alkyl ether amine, an amphoteric surfactant) and Resanol Bal (N-3-tridecyloxy propyl 1-3 diamine, branched acetate) pyrite floated at high pH values. It was shown that amine type collectors could be efficient to selectively float pyrite from chalcopyrite at alkali pH ranges in the case of ore samples.
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 5; 15-22
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pyrite flotation in the presence of galena. Study on galvanic interaction
Autorzy:
Allahkarami, E.
Poor, A. Z.
Rezai, B.
Powiązania:
https://bibliotekanauki.pl/articles/110735.pdf
Data publikacji:
2017
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
flotation
galena
pyrite
galvanic interactions
Opis:
In this investigation, galvanic interaction between galena and pyrite in flotation and its effect on floatability of pyrite were studied. Rest and mixed potential studies in the presence and absence of a collector indicated that pyrite was nobler than galena under all investigated conditions. Therefore, pyrite served as a cathode in galvanic interactions with galena. Floatability of pyrite was performed alone and as a mixture with galena in the ratios of pyrite to galena equal to 1:4, 1:1 and 4:1. The experiments were conducted with air and nitrogen. In any galvanic contact between pyrite and galena, anodic oxidation occurred on the galena surface, and hydrolysed lead species adsorbed on the pyrite surface. The investigation of the various reactions occurring on the sample surface was investigated by ethylene diamine-tetra acetic acid disodium salt (EDTA) extraction and X-ray photoelectron spectroscopy (XPS) measurements. In the presence of nitrogen, floatability of pyrite increased. The recovery of pyrite in the presence of air was 22%, while in the mixture with galena (ratio 1:4) the recovery increased to 43%. The results indicated that the presence of galena improved floatability of pyrite.
Źródło:
Physicochemical Problems of Mineral Processing; 2017, 53, 2; 846-858
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption mechanism of copper xanthate on pyrite surfaces
Autorzy:
Deng, Zhengbin
Cheng, Wanli
Tang, Yun
Tong, Xiong
Liu, Zhihong
Powiązania:
https://bibliotekanauki.pl/articles/1447276.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
pyrite
cupric xanthate
cuprous xanthate
adsorption
surface
Opis:
The ratio of the hydrophobic to hydrophilic species and their distribution on mineral surfaces significantly influences the floatability of sulfide minerals. Through the flotation test, the influence of different reagents on pyrite flotation was examined. The interaction mechanisms between copper xanthate and pyrite were evaluated using advanced analysis technologies, including contact angle measurements, zeta potential analysis, scanning electron microscopy, energy dispersive spectroscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The results show that the butyl xanthate in solution reacts with copper sulfate to form cupric xanthate, increasing the consumption of the collector butyl xanthate and resulting in lower floatability of pyrite. Cupric xanthate can be adsorbed on the pyrite surface through bonding with the sulfur sites. The adsorbed cupric xanthate on the pyrite surface undergoes redox reaction. The cupric xanthate is reduced to cuprous xanthate, and the sulfur on the surface will be oxidized. The adsorption products on the pyrite surface contain both cuprous xanthate and cupric xanthate. As the pH of a solution increases, the absolute value of the zeta potential of pyrite surface increased and the surface contact angle increased. Iron xanthate is also formed on the pyrite surface through a chemical reaction between the xanthate ions and pyrite, oxidation of xanthate ions to dixanthogen also takes place. Cuprous xanthate is the main hydrophobic substance on the pyrite surface, which can change the surface electrical properties and wettability of pyrite, and improve hydrophobicity of pyrite.
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 3; 46-60
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption Behavior of Glucuronic Acid on Pyrite Surface: an electrochemical and DFT Study
Autorzy:
Ning, Xu Jia
Ying, Yang Hong
Lin, Tong-Lin
Powiązania:
https://bibliotekanauki.pl/articles/355049.pdf
Data publikacji:
2020
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
glucuronic acid
pyrite
adsorption
Opis:
Bacterial adsorption on mineral surface is one of the key steps in bioleaching process. The bacteria adsorb on the mineral surface via the extracellular polymeric substances (EPS) layer. In this paper, the behavior of glucuronic acid, one of the key substances in EPS layer, adsorbed on the pyrite surface is studied using DFT and electrochemical methods. Adsorption capacity of glucuronic acid is stronger than that of water. Glucuronic acid adsorbs on pyrite surfaces and it follows a mixed type of interactions (physisorption and chemisorption). Adsorption of glucuronic acid on pyrite surface followed Langmuir’s adsorption isotherm with adsorption standard free energy of –27.67kJ mol-1. The structural and electronic parameters were calculated and discussed.
Źródło:
Archives of Metallurgy and Materials; 2020, 65, 1; 433-440
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mineralogical and morphological studies of gold-bearing arsenopyrite and pyrite minerals of Bakyrchik and Bolshevik gold black shale deposits (Eastern Kazakhstan)
Autorzy:
Junussov, M.
Umarbekova, Z.
Powiązania:
https://bibliotekanauki.pl/articles/100802.pdf
Data publikacji:
2018
Wydawca:
Uniwersytet Śląski. Wydział Nauk o Ziemi
Tematy:
Bakyrchik
gold-bearing arsenopyrite and pyrite
acicular-prismatic arsenopyrite
cubic pyrite
złoże
arsenopiryt
złoto
piryt
skład chemiczny
metoda badań
Opis:
Bakyrchik and Bolshevik both are sediment-hosted disseminated gold deposits. They are located in Eastern Kazakhstan (4 km in distance between deposits) and include in the Western Qalba metallogenic zone. They originated in late Paleozoic age along structured line between palaeocontinents of Kazakhstan and Altai-Mongol. The purpose of this paper is designation of typomorphic features of gold-bearing arsenopyrite and pyrite minerals, determination of chemical composition of these two sulfides minerals. The arsenopyrite and pyrite are the main objects for analytical study of gold-bearing sulfide minerals, their different textures, morphology of the crystals and aggregates. The studies of ore samples and minerals were carried out by methods of optical microscope, X-ray diffraction, X-ray fluorescence and electron microprobe analyses. The analytical study of sulphide minerals has shown that the arsenopyrite is acicular and tabular, pyrite has three varieties - globular, hexahedral and pentahedral forms in three rock samples of the carbonaceous-terrigenous formation in the deposits.
Źródło:
Contemporary Trends in Geoscience; 2018, 7, 2; 153-165
2299-8179
Pojawia się w:
Contemporary Trends in Geoscience
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A study on the effect of active pyrite on flotation of porphyry copper ores
Autorzy:
Molaei, N.
Hoseinian, F. S.
Rezai, B.
Powiązania:
https://bibliotekanauki.pl/articles/109515.pdf
Data publikacji:
2018
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
flotation
optimization
collector
chalcopyrite
active pyrite
Opis:
Active pyrite is one of the most undesirable phenomena in the flotation of porphyry copper ores. Misreported pyrite into copper concentrates decreased the grade and recovery of copper. In this study, the effective parameters on the flotation process including grinding condition and chemical parameters were evaluated in order to decrease the active pyrite recovery by flotation. Firstly, optical microscopic and grinding studies were carried out to determine the optimal particle size and grinding time. The results showed that 43 minutes of grinding is necessary to achieve the optimum liberation degree of 53 µm for flotation. Then, the flotation effective parameters such as pH (7.3, 10, 10.5, 11, 11.5 and 12), collector type (Nascol, Aero 407, Aero 3477 and X231), collector concentration (12 and 25 mg/dm3), depressant concentration (0 and 25 mg/dm3) and frother concentration (0 and 25 mg/dm3) were investigated in a Denver-type laboratory flotation cell with a constant capacity of 2.5 dm3. The results showed that the optimal conditions for chalcopyrite flotation were pH of 11.5, Aero 407 as a collector with concentration of 25 mg/dm3, Dowfroth 250 (DF250) as a frother with concentration of 25 mg/dm3 and Na2SO3 as a depressant with concentration of 25 mg/dm3. The type of collector had greater effect on the chalcopyrite flotation than the other parameters. The recovery and grade of chalcopyrite and pyrite were obtained as 79.95%, 49% and 5.3%, 7.98% using the Aero 407, respectively. Under the optimum conditions, the grade of final concentrate increased from 0.94% to 21.3% with three cleaner stages.
Źródło:
Physicochemical Problems of Mineral Processing; 2018, 54, 3; 922-933
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pyrite oxidation inhibition by hydrophobic films for acid mine drainage control at the source
Autorzy:
Wang, Shuncai
Zhao, Yue
Li, Shuang
Powiązania:
https://bibliotekanauki.pl/articles/110200.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
hydrophobic film
pyrite
suppression
linoleic acid
acid mine drainage
Opis:
Acid mine drainage (AMD), which is also known as acid rock drainage (ARD), can cause serious environmental pollution, especially for surrounding aquatic and terrestrial ecosystems due toits low pH, high metal and sulfate concentration. Acid mine drainage is an urgent environmental problem for the worldwide ore mining industry. In this paper, we demonstrated that hydrophobic films can inhibit the oxidation of pyrite-bearing tailings to achieve the control of at-source AMD. The results of chemical leaching testing showed that the hydrophobic films formed by linoleic acid can suppress the oxidation of pyrite-bearing tailings and reduce the AMD production. In addition, the presence of hydrophobic films of linoleic acid on the surface of pyrite-bearing tailings was confirmed by the results from Fourier transform infrared (FTIR) analyses and scanning electron microscopy with energy dispersive spectrometry (SEM / EDS).
Źródło:
Physicochemical Problems of Mineral Processing; 2019, 55, 5; 1132-1140
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
First-principles study on the adsorption structure of water molecules on a pyrite (100) surface
Autorzy:
Liu, Yingchao
Chen, Jianhua
Li, Yuqiong
Zhang, Junjie
Kang, Duan
Powiązania:
https://bibliotekanauki.pl/articles/1447970.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
pyrite
water molecules
adsorption
Opis:
The hydration structure of water molecule adsorption at different coverages of a monolayer on a pyrite (100) surface were simulated using the density functional theory (DFT) method. The results demonstrate that the Fe-O interaction weakens and the adsorption energy per water molecule decreases with increasing water coverage, except at a monolayer coverage of 12/12 (i.e., full coverage). H-S and H-O hydrogen bonds were formed on the nearest surface layer. When large amounts of water molecules adsorb onto the surface, the adsorbed water molecules can be divided into three layers: the layer nearest to the surface, the second nearest to the surface, and the layer farthest from the surface. The thickness of the former two layers is approximately 5.5 Å. The three layers have water densities of 1.12 g/cm3, 1.08 g/cm3, and 0.95 g/cm3, respectively, suggesting that there is a strong interaction between the pyrite surface and water molecules and the influence of surface structure on water adsorption reaches a distance of more than 10 Å. Dynamics simulations suggest that the water molecules close to the mineral surfaces are in an orderly arrangement while those far from the surface are disordered.
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 2; 121-130
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Impact of ovalbumin on pyrite flotation in the absence and presence of metal ions
Autorzy:
Guler, T.
Sahbudak, K.
Akdemir, U.
Cetinkaya, S.
Powiązania:
https://bibliotekanauki.pl/articles/110499.pdf
Data publikacji:
2014
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
pyrite
ovalbumin
metal ion
flotation
redox potential
Opis:
Recovery of gangue pyrite and its accidental activation are vital issues in flotation of complex sulfide ores. This work was performed by cyclic voltammetry (CV) and flotation tests to elucidate applicability of ovalbumin (OVA) as depressant for pyrite. The synergetic effect of metal ions in addition to its possible use in case of accidental activation by metal ions. CV tests stated that OVA adsorbed irreversibly on pyrite, and restricted electron transfer up to moderately oxidizing potentials due to electrostatic interaction together with weak hydrophobic interactions. At highly oxidizing potentials, adsorption occurred through electrochemical mechanisms through formation of metal-OVA chelates. Rate of pyrite depression with OVA was found to be potential dependent reaching its peak point around moderately oxidizing potentials both in absence and presence of metal ions. Electrochemically active metals display synergetic effect with OVA on pyrite depression, whereas noble metals activate pyrite and reduced depressing potency of OVA.
Źródło:
Physicochemical Problems of Mineral Processing; 2014, 50, 1; 31-40
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption of yeast dextran on clinochlore surface and the implications for pyrite/clinochlore separation
Autorzy:
Wang, Zhen
Zou, Dan
Zhao, Kaile
Safarov, Sayfidin
Xu, Ying
Powiązania:
https://bibliotekanauki.pl/articles/2146917.pdf
Data publikacji:
2022
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
clinochlore
pyrite
flotation
yeast dextran
adsorption
Opis:
Silicate minerals with a certain degree of flotability are often easy to mix into sulfide ore concentrate in mineral processing industry. In this paper, the adsorption of yeast dextran on clinochlore and its application in pyrite/clinochlore separation were investigated. The adsorbed amount and micro polarity measurement results displayed that the yeast dextran molecules selectively adsorbed onto clinochlore surface compared with pyrite. The adsorbed yeast dextran resulted in the increase in the surface polarity of clinochlore surface, and inhibited the further adsorption of xanthate, thus keep it hydrophilic and depressed. Quantum chemical computation results indicated that yeast dextran was mainly adsorbed on mineral surface by the chelation with the surface metal active sites, and the chelating strength of yeast dextran with three ions was in the sequence of Fe3+ > Mg2+ > Fe2+. While Mg2+, Fe2+ and Fe3+ are the main metal ions on the surface of clinochlore, and Fe2+ is the unique metal ions on pyrite surface. This is the reason of the selectivity of the yeast dextran depressant for pyrite/clinochlore flotation system. The flotation results demonstrated that yeast dextran was qualified to selectively depress clinochlore in pyrite flotation.
Źródło:
Physicochemical Problems of Mineral Processing; 2022, 58, 4; art. no. 151635
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
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