Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.06.006
M. Khayar , J. Bessière
It is possible to analyze in situ the adsorbate/adsorbant interaction during the flotation process by high frequency dielectric measurements. The adsorption of complexing collector (sodium oleate) onto calcite increases the dielectric permittivity independently of the frequency. The dielectric constant increases after adsorption because the adsorbate and the adsorbant interact through covalent bonds. Physical adsorption involving electrostatic interactions or hydrogen bonds (dodecylamine and dodecylsulfate) has no effect on the dielectrical characteristics. The dielectric method allows to analyze the mechanisms of depression using reagents such as quebracho and sodium silicate.
{"title":"Study of the adsorption of collectors and depressants onto calcite by high frequency dielectric measurements","authors":"M. Khayar , J. Bessière","doi":"10.1016/j.minpro.2017.06.006","DOIUrl":"10.1016/j.minpro.2017.06.006","url":null,"abstract":"<div><p><span>It is possible to analyze in situ the adsorbate/adsorbant interaction during the flotation<span> process by high frequency dielectric measurements. The adsorption of complexing collector (sodium oleate) onto calcite<span> increases the dielectric permittivity independently of the frequency. The dielectric constant increases after adsorption because the adsorbate and the adsorbant interact through covalent bonds. Physical adsorption involving electrostatic interactions or </span></span></span>hydrogen bonds<span> (dodecylamine and dodecylsulfate) has no effect on the dielectrical characteristics. The dielectric method allows to analyze the mechanisms of depression using reagents such as quebracho and sodium silicate.</span></p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.06.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48838936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.07.001
Ataollah Nosrati , Mikael Larsson , Johan B. Lindén , Zhang Zihao , Jonas Addai-Mensah , Magnus Nydén
To date, the quest for cost-effective methods for removal of dissolved metals from aqueous solutions remains a daunting challenge for many industries. This paper reports on the development of an effective, hybrid adsorbent for selective copper recovery from aqueous solutions under industrially relevant conditions. The work involved (i) purification and functionalization of diatomaceous earth (DE) particles with glutaraldehyde(GA)-crosslinked polyethyleneimine(PEI), (ii) physicochemical characterization of the product and (iii) metal adsorption from solutions containing Cu(II)/Ni(II)/Fe(II)/Ca(II)/Mg(II)/Mn(II)/Al(III)/Na ions and their subsequent elution behaviour. Acid leaching of the pristine DE led to a significant reduction in its metal oxide (e.g., Al2O3, Fe2O3) constituents and a concomitant increase in both SiO2 content and specific surface area. Upon functionalization with GA-crosslinked PEI, the DE particles' interfacial chemistry was completely altered to that of the polymer with no change in specific surface area. Isothermal batch adsorption from saline (15 g/dm3 NaCl) and non-saline solutions containing 500 and 1000 mg/dm3 of Cu at ~ pH 4 revealed > 97% Cu(II) removal by functionalized DE within 3 min in both cases. Subsequent water elution tests at pH 1 showed complete release of the adsorbed Cu confirming pH-dependent interaction between dissolved Cu and GA-crosslinked PEI. The preliminary batch adsorption/elution tests involving 1000 mg/dm3 solutions of Ni, Ca, Mg, Mn, Fe, Na and Al showed little or negligible affinity of the functionalized DE towards these elements, suggesting good selectivity for Cu. Furthermore, it is shown that the functionalized particles are chemically stable at H2SO4 concentrations up to 2 M and may be recycled > 10 times without loss in their Cu adsorption/desorption performance.
{"title":"Polyethyleneimine functionalized mesoporous diatomite particles for selective copper recovery from aqueous media","authors":"Ataollah Nosrati , Mikael Larsson , Johan B. Lindén , Zhang Zihao , Jonas Addai-Mensah , Magnus Nydén","doi":"10.1016/j.minpro.2017.07.001","DOIUrl":"10.1016/j.minpro.2017.07.001","url":null,"abstract":"<div><p><span><span>To date, the quest for cost-effective methods for removal of dissolved metals from aqueous solutions remains a daunting challenge for many industries. This paper reports on the development of an effective, hybrid adsorbent for selective copper recovery from aqueous solutions under industrially relevant conditions. The work involved (i) purification and functionalization of diatomaceous earth<span> (DE) particles with glutaraldehyde(GA)-crosslinked polyethyleneimine(PEI), (ii) physicochemical characterization of the product and (iii) metal adsorption from solutions containing Cu(II)/Ni(II)/Fe(II)/Ca(II)/Mg(II)/Mn(II)/Al(III)/Na ions and their subsequent elution behaviour. Acid leaching of the pristine DE led to a significant reduction in its </span></span>metal oxide (e.g., Al</span><sub>2</sub>O<sub>3</sub>, Fe<sub>2</sub>O<sub>3</sub>) constituents and a concomitant increase in both SiO<sub>2</sub> content and specific surface area. Upon functionalization with GA-crosslinked PEI, the DE particles' interfacial chemistry was completely altered to that of the polymer with no change in specific surface area. Isothermal batch adsorption from saline (15<!--> <!-->g/dm<sup>3</sup> NaCl) and non-saline solutions containing 500 and 1000<!--> <!-->mg/dm<sup>3</sup> of Cu at ~<!--> <!-->pH<!--> <!-->4 revealed ><!--> <!-->97% Cu(II) removal by functionalized DE within 3<!--> <!-->min in both cases. Subsequent water elution tests at pH<!--> <!-->1 showed complete release of the adsorbed Cu confirming pH-dependent interaction between dissolved Cu and GA-crosslinked PEI. The preliminary batch adsorption/elution tests involving 1000<!--> <!-->mg/dm<sup>3</sup><span> solutions of Ni, Ca, Mg, Mn, Fe, Na and Al showed little or negligible affinity of the functionalized DE towards these elements, suggesting good selectivity for Cu. Furthermore, it is shown that the functionalized particles are chemically stable at H</span><sub>2</sub>SO<sub>4</sub> concentrations up to 2<!--> <!-->M and may be recycled ><!--> <!-->10 times without loss in their Cu adsorption/desorption performance.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42070678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.07.006
Jia Tian , Longhua Xu , Yaohui Yang , Jing Liu , Xiaobo Zeng , Wei Deng
The flotation behavior of ilmenite and titanaugite using anionic collector sodium oleate (NaOL), cationic collector dodecylamine acetate (DAA) and the mixed anionic/cationic collector (NaOL-DAA) was investigated through micro-flotation experiments, zeta potential measurements, Fourier transform infrared (FTIR) analyses, and the artificially mixed minerals flotation experiments. The results of the microflotation experiments indicate that DAA exhibits good flotation performance to both ilmenite and titanaugite at a pH > 6.0. The flotation separation of ilmenite from titanaugite can be performed using the mixed NaOL-DAA in a wide pH range of 5.0–7.0. In this pH range, the recovery of ilmenite remains constant at approximately 90%, while the recovery of titanaugite remains < 25%. The best separation result can be achieved with NaOL-DAA molar ratios of 10:1. The results of the zeta potential experiments and the FTIR analyses indicate that the adsorption of the mixed collector, NaOL-DAA, on the ilmenite surface is larger than on the titanaugite surface and that the NaOL-DAA complex might be mainly adsorbed on the ilmenite surface by chemical adsorption, apart from electrostatic adsorption. The synthetic mineral mixture micro-flotation results demonstrate that, compared to NaOL, NaOL-DAA not only increases the recovery and grade of the TiO2 by 7.02% and 6.71%, respectively, but also decreases the reagent consumption by half.
{"title":"Selective flotation separation of ilmenite from titanaugite using mixed anionic/cationic collectors","authors":"Jia Tian , Longhua Xu , Yaohui Yang , Jing Liu , Xiaobo Zeng , Wei Deng","doi":"10.1016/j.minpro.2017.07.006","DOIUrl":"10.1016/j.minpro.2017.07.006","url":null,"abstract":"<div><p><span><span>The flotation behavior of </span>ilmenite<span> and titanaugite using anionic collector sodium oleate (NaOL), cationic collector dodecylamine acetate (DAA) and the mixed anionic/cationic collector (NaOL-DAA) was investigated through micro-flotation experiments, zeta potential measurements, Fourier transform infrared (FTIR) analyses, and the artificially mixed minerals flotation experiments. The results of the microflotation experiments indicate that DAA exhibits good flotation performance to both ilmenite and titanaugite at a pH</span></span> <!-->><!--> <!-->6.0. The flotation separation of ilmenite from titanaugite can be performed using the mixed NaOL-DAA in a wide pH range of 5.0–7.0. In this pH range, the recovery of ilmenite remains constant at approximately 90%, while the recovery of titanaugite remains <<!--> <span>25%. The best separation result can be achieved with NaOL-DAA molar ratios of 10:1. The results of the zeta potential experiments and the FTIR analyses indicate that the adsorption of the mixed collector, NaOL-DAA, on the ilmenite surface is larger than on the titanaugite surface and that the NaOL-DAA complex might be mainly adsorbed on the ilmenite surface by chemical adsorption, apart from electrostatic adsorption. The synthetic mineral mixture micro-flotation results demonstrate that, compared to NaOL, NaOL-DAA not only increases the recovery and grade of the TiO</span><sub>2</sub> by 7.02% and 6.71%, respectively, but also decreases the reagent consumption by half.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47754264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.07.009
A. Farzanegan , N. Khorasanizadeh , Gh.A. Sheikhzadeh , H. Khorasanizadeh
In this research, a numerical approach and a series of laboratory tests have been used to investigate the effect of vertical baffling and height to diameter ratio on the axial mixing in flotation columns. The baffle is a plate located perpendicular to the cross section of the column with a length of 2.8 m and thickness of 0.4 cm. The computational domain is a column with a circular cross section having a height of 3.2 m and a diameter of 10 cm. Three-dimensional simulations were executed using Eulerian two-phase computational fluid dynamics (CFD) models for both non-baffled and baffled columns. In order to reduce computing demand and simplify the problem, it was assumed that the column is already filled with water, and air enters from the lateral and upper surfaces of a cylindrical sparger with a length of 15 cm and a diameter of 1 cm located vertically at the bottom of the column. To validate the simulation results, a series of laboratory flotation column experiments have been performed under the above-mentioned conditions. Three-dimensional simulations were executed using an Eulerian two-phase model for both non-baffled and baffled columns. The simulated pressure values on the wall at 0.2 m and 2.8 m height of the non-baffled column were in good agreement with experimentally measured values with the highest relative difference of < 3.07%. Comparison of the computational results for the non-baffled and baffled columns showed that baffling can reduce water axial velocity up to 16.96%, which consequently reduces the axial mixing in the column and increases flotation recovery. Study of the effects of height to diameter ratio showed that effect of baffling in columns with lower aspect ratios is more prevalent for reducing the axial mixing.
{"title":"Laboratory and CFD investigations of the two-phase flow behavior in flotation columns equipped with vertical baffle","authors":"A. Farzanegan , N. Khorasanizadeh , Gh.A. Sheikhzadeh , H. Khorasanizadeh","doi":"10.1016/j.minpro.2017.07.009","DOIUrl":"10.1016/j.minpro.2017.07.009","url":null,"abstract":"<div><p><span>In this research, a numerical approach and a series of laboratory tests have been used to investigate the effect of vertical baffling and height to diameter ratio on the axial mixing in flotation columns. The baffle is a plate located perpendicular to the cross section of the column with a length of 2.8</span> <!-->m and thickness of 0.4<!--> <!-->cm. The computational domain is a column with a circular cross section having a height of 3.2<!--> <!-->m and a diameter of 10<!--> <!-->cm. Three-dimensional simulations were executed using Eulerian two-phase computational fluid dynamics (CFD) models for both non-baffled and baffled columns. In order to reduce computing demand and simplify the problem, it was assumed that the column is already filled with water, and air enters from the lateral and upper surfaces of a cylindrical sparger with a length of 15<!--> <!-->cm and a diameter of 1<!--> <!-->cm located vertically at the bottom of the column. To validate the simulation results, a series of laboratory flotation column experiments have been performed under the above-mentioned conditions. Three-dimensional simulations were executed using an Eulerian two-phase model for both non-baffled and baffled columns. The simulated pressure values on the wall at 0.2<!--> <!-->m and 2.8<!--> <!-->m height of the non-baffled column were in good agreement with experimentally measured values with the highest relative difference of <<!--> <span>3.07%. Comparison of the computational results for the non-baffled and baffled columns showed that baffling can reduce water axial velocity up to 16.96%, which consequently reduces the axial mixing in the column and increases flotation recovery. Study of the effects of height to diameter ratio showed that effect of baffling in columns with lower aspect ratios is more prevalent for reducing the axial mixing.</span></p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44933962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.06.008
Shekwonyadu Iyakwari , Hylke J. Glass , Stephen E. Obrike
The preconcentration or early rejection of gangue minerals in mineral processing operations is investigated using sorting, based on interpretation of near infrared sensor data collected from ore particles. The success of sorting depends on the distribution of minerals between particles, the arrangement or association of minerals within particles and the ability of near infrared to distinguish relevant minerals. This paper considers minerals association, using common alteration minerals found in a hydrothermally-formed copper ore, with sensitivity in the near infrared region. The selected NIR-active minerals were arranged along the view of NIR line scanner to stimulate adjacent natural minerals association.
It was found that spectral dominance may depend on minerals near infrared sensitivity and or the position of a mineral along the NIR scanner line of view. Analysis also revealed that only free occurring waste mineral spectra can be targeted for discrimination as tailings. Where spectra appeared mixed, such spectra are best considered products.
{"title":"Discerning mineral association in the near infrared region for ore sorting","authors":"Shekwonyadu Iyakwari , Hylke J. Glass , Stephen E. Obrike","doi":"10.1016/j.minpro.2017.06.008","DOIUrl":"10.1016/j.minpro.2017.06.008","url":null,"abstract":"<div><p>The preconcentration or early rejection of gangue minerals in mineral processing<span><span> operations is investigated using sorting, based on interpretation of near infrared sensor data collected from ore particles. The success of sorting depends on the distribution of minerals between particles, the arrangement or association of minerals within particles and the ability of near infrared to distinguish relevant minerals. This paper considers minerals association, using common alteration minerals found in a hydrothermally-formed </span>copper ore, with sensitivity in the near infrared region. The selected NIR-active minerals were arranged along the view of NIR line scanner to stimulate adjacent natural minerals association.</span></p><p>It was found that spectral dominance may depend on minerals near infrared sensitivity and or the position of a mineral along the NIR scanner line of view. Analysis also revealed that only free occurring waste mineral spectra can be targeted for discrimination as tailings. Where spectra appeared mixed, such spectra are best considered products.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.06.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42701951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.07.010
E.L. Thyse , G. Akdogan , A. Mainza , J. Eksteen
There is little in-depth study on the downstream processing characteristics of granulated PGM-containing converter matte, particularly related to grinding and liberation behavior closely associated with leaching, and also as a function of iron endpoint specific mineralogy. Moreover, there is limited physical property data available, such as hardness and breakage of converter matte mineral structures that allows for considering a possible dependence between the mineralogy and the downstream processing characteristics of converter matte. The aim of this study was to investigate a relationship between indentation hardness, breakage and the mineralogy of two different iron end point converter mattes namely Fe_0.15% and Fe_5.17%. This also allowed for a subsequent investigation to relate the mineralogy to the integrated downstream processing characteristics of granulated converter matte.
A Nano-indentation tester was used to measure the indentation hardness of mineral structures. The indentation system also had the ability to test the breakage characteristics of the respective mineral structures by applying a preset load. Laboratory batch grinding tests were conducted at various specific energies with respect to granulated high and low iron mattes. A high resolution field-emission scanning electron microscope was utilized for mineralogical analysis. The perfect mixing ball mill model was subsequently used to assess the breakage rates of matte particles and minerals. A mineral liberation analyzer was used to investigate the liberation characteristics of mineral structures of interest.
The investigations revealed that the minerals and associated boundaries showed relatively different indentation hardness. The indentation-induced breakage of nickel sulfide, copper sulfide and NiCu-alloy structures appeared preferential and related to the iron end point. The softest mineral was found to be copper sulfide, which exhibited the average indentation hardness of 1975 and 2978 MPa within the low and high iron matte respectively. The increasingly harder minerals were nickel sulfide and NiCu-alloy in both low and high iron mattes with mean values around 5000 MPa. The laboratory batch grinding of the converter mattes at specific energy inputs resulted in product size distributions correlated to the underlying mineralogy. Although the trends for the breakage rates was found to be similar for both mattes, the matte with Fe content of 5.17% exhibited higher breakage rates in the specific energy ranges from 5 kWh/t to 25 kWh/t. This indicated that the matte with 5.17% Fe produces finer product than that of the 0.15% Fe matte at the same energy level. Moreover, a higher degree of overall liberation was achieved for copper sulfide and NiCu-alloy present within the high iron matte particles compared to particles within the low iron matte. 40% of particles within the high iron matte are comple
{"title":"PGM converter matte mineral characteristics and effects on downstream processing","authors":"E.L. Thyse , G. Akdogan , A. Mainza , J. Eksteen","doi":"10.1016/j.minpro.2017.07.010","DOIUrl":"10.1016/j.minpro.2017.07.010","url":null,"abstract":"<div><p><span>There is little in-depth study on the downstream processing characteristics of granulated PGM-containing converter matte, particularly related to grinding and liberation behavior closely associated with leaching, and also as a function of iron endpoint specific </span>mineralogy. Moreover, there is limited physical property data available, such as hardness and breakage of converter matte mineral structures that allows for considering a possible dependence between the mineralogy and the downstream processing characteristics of converter matte. The aim of this study was to investigate a relationship between indentation hardness, breakage and the mineralogy of two different iron end point converter mattes namely Fe_0.15% and Fe_5.17%. This also allowed for a subsequent investigation to relate the mineralogy to the integrated downstream processing characteristics of granulated converter matte.</p><p>A Nano-indentation tester was used to measure the indentation hardness of mineral structures. The indentation system also had the ability to test the breakage characteristics of the respective mineral structures by applying a preset load. Laboratory batch grinding tests were conducted at various specific energies with respect to granulated high and low iron mattes. A high resolution field-emission scanning electron microscope was utilized for mineralogical analysis. The perfect mixing ball mill model was subsequently used to assess the breakage rates of matte particles and minerals. A mineral liberation analyzer was used to investigate the liberation characteristics of mineral structures of interest.</p><p><span>The investigations revealed that the minerals and associated boundaries showed relatively different indentation hardness. The indentation-induced breakage of nickel sulfide, copper sulfide and NiCu-alloy structures appeared preferential and related to the iron end point. The softest mineral was found to be copper sulfide, which exhibited the average indentation hardness of 1975 and 2978</span> <!-->MPa within the low and high iron matte respectively. The increasingly harder minerals were nickel sulfide and NiCu-alloy in both low and high iron mattes with mean values around 5000<!--> <!-->MPa. The laboratory batch grinding of the converter mattes at specific energy inputs resulted in product size distributions correlated to the underlying mineralogy. Although the trends for the breakage rates was found to be similar for both mattes, the matte with Fe content of 5.17% exhibited higher breakage rates in the specific energy ranges from 5<!--> <!-->kWh/t to 25<!--> <!-->kWh/t. This indicated that the matte with 5.17% Fe produces finer product than that of the 0.15% Fe matte at the same energy level. Moreover, a higher degree of overall liberation was achieved for copper sulfide and NiCu-alloy present within the high iron matte particles compared to particles within the low iron matte. 40% of particles within the high iron matte are comple","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.010","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47872921","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The pressure oxidation process to prepare sodium pyroantimonate from sodium thioantimonite solution was optimized. The results indicate that increasing reaction temperature, oxygen partial pressure and stirring speed can significantly accelerate the oxidation precipitation rate of Sb. A decrease in Sb3 + concentration is beneficial for shortening the reaction time. The NaOH concentration has no significant effect on the oxidation velocity but plays an important role in the quality of sodium pyroantimonate. An increase in stirring speed and oxygen partial pressure result in the formation of a red precipitation in the solution with 12.5 g/L of NaOH, while the desired sodium pyroantimonate can be produced with a NaOH concentration of 30.0 g/L. The XRD and SEM-EDS analysis confirm that the red precipitate is composed of NaSb(OH)6 and Na6Sb4S9.
{"title":"Optimization of pressure oxidation process to prepare sodium pyroantimonate from sodium thioantimonite solution","authors":"Tianzu Yang, Hongbin Ling, Duchao Zhang, Yuntao Guo, Weifeng Liu, Lin Chen, Shuai Rao","doi":"10.1016/j.minpro.2017.07.002","DOIUrl":"10.1016/j.minpro.2017.07.002","url":null,"abstract":"<div><p><span>The pressure oxidation process to prepare sodium pyroantimonate from sodium thioantimonite solution was optimized. The results indicate that increasing reaction temperature, oxygen partial pressure and stirring speed can significantly accelerate the oxidation precipitation rate of Sb. A decrease in Sb</span><sup>3<!--> <!-->+</sup> concentration is beneficial for shortening the reaction time. The NaOH concentration has no significant effect on the oxidation velocity but plays an important role in the quality of sodium pyroantimonate. An increase in stirring speed and oxygen partial pressure result in the formation of a red precipitation in the solution with 12.5<!--> <!-->g/L of NaOH, while the desired sodium pyroantimonate can be produced with a NaOH concentration of 30.0<!--> <!-->g/L. The XRD and SEM-EDS analysis confirm that the red precipitate is composed of NaSb(OH)<sub>6</sub> and Na<sub>6</sub>Sb<sub>4</sub>S<sub>9</sub>.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48926849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-10DOI: 10.1016/j.minpro.2017.07.003
Jingjing Xiao, Guangyi Liu, Hong Zhong
In this paper, a novel surfactant, N-butoxypropyl-S-[2-(hydroxyimino) propyl] dithiocarbamate ester (BOPHPDT) was first synthesized and introduced as a flotation collector for copper minerals. The micro and bench-scale flotation results demonstrated BOPHPDT exhibited superior flotation performance for chalcopyrite in comparison with xanthates and excellent selectivity against pyrite, and the preferable pH values for its attachment to chalcopyrite surfaces were 4–8. Adsorption thermodynamics and kinetics elucidated that BOPHPDT adsorption on to chalcopyrite was a spontaneously endothermic chemisorption process. The results of in situ scanning electrochemical microscopy (SECM) and zeta potential showed that BOPHPDT might anchor on the positively charge sites of chalcopyrite surfaces to form new species. Fourier transform infrared (FTIR) spectra further elucidated that BOPHPDT might react with the Cu atoms of chalcopyrite surfaces through its CNOH and NHC(S) groups. The double chelating groups and multiple hydrophobic chains of BOPHPDT, rendered it to possess excellent affinity and hydrophobicity for improving copper minerals flotation.
本文首次合成了一种新型表面活性剂n -丁氧基丙基- s -[2-(羟亚胺)丙基]二硫代氨基甲酸酯(BOPHPDT),并将其作为铜矿物的浮选捕收剂。微观和实验尺度浮选结果表明,BOPHPDT对黄铜矿的浮选性能优于黄药,对黄铁矿具有良好的选择性,其与黄铜矿表面的吸附pH值为4 ~ 8。吸附热力学和动力学表明,BOPHPDT对黄铜矿的吸附是一个自发吸热的化学吸附过程。原位扫描电化学显微镜(SECM)和zeta电位结果表明,BOPHPDT可能锚定在黄铜矿表面的正电荷位点上形成新的物质。傅里叶变换红外光谱(FTIR)进一步证实BOPHPDT可能通过其CNOH和NHC(S)基团与黄铜矿表面的Cu原子发生反应。BOPHPDT具有双螯合基团和多条疏水链,对改善铜矿物浮选具有良好的亲和疏水性。
{"title":"The adsorption mechanism of N-butoxypropyl-S-[2-(hydroxyimino) propyl] dithiocarbamate ester to copper minerals flotation","authors":"Jingjing Xiao, Guangyi Liu, Hong Zhong","doi":"10.1016/j.minpro.2017.07.003","DOIUrl":"10.1016/j.minpro.2017.07.003","url":null,"abstract":"<div><p><span>In this paper, a novel surfactant, </span><em>N</em>-butoxypropyl-<em>S</em><span><span><span>-[2-(hydroxyimino) propyl] dithiocarbamate ester (BOPHPDT) was first synthesized and introduced as a flotation collector for copper minerals. The micro and bench-scale flotation results demonstrated BOPHPDT exhibited superior flotation performance for </span>chalcopyrite in comparison with xanthates and excellent </span>selectivity<span> against pyrite, and the preferable pH values for its attachment to chalcopyrite surfaces were 4–8. Adsorption thermodynamics and kinetics elucidated that BOPHPDT adsorption on to chalcopyrite was a spontaneously endothermic chemisorption process. The results of </span></span><em>in situ</em><span> scanning electrochemical microscopy (SECM) and zeta potential showed that BOPHPDT might anchor on the positively charge sites of chalcopyrite surfaces to form new species. Fourier transform infrared (FTIR) spectra further elucidated that BOPHPDT might react with the Cu atoms of chalcopyrite surfaces through its C</span><img>N<img>OH and NH<img>C(<img><span>S) groups. The double chelating groups and multiple hydrophobic chains of BOPHPDT, rendered it to possess excellent affinity and hydrophobicity for improving copper minerals flotation.</span></p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.07.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45076950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Co-reduction roasting of seaside titanomagnetite and blast furnace dust was investigated to maximize the use of these ores in Indonesia. This direct reduction process utilizes fixed carbon in BFD to reduce iron from BFD and titanomagnetite. X-ray diffraction and X-ray fluorescence analyses were performed to characterize the reduced iron powder. The influences of reduction conditions, such as reduction temperature and duration, C/Fe molar ratio, grinding fineness and fluorite dose, on the indicators of reduced iron powder were evaluated. Fixed carbon and volatile matter contents were lower in BFD than those in coal. However, reduction and separation of titanium and iron exhibited similar effects on reduction roasting. Results showed that the optimum conditions of roasting reduction included C/Fe molar ratio of 0.65, fluorite dose of 4 mass%, and roasting temperature of 1300 °C for 60 min. The reduced iron powder was obtained through two-stage grinding and two-stage magnetic separation of the roasted product. The former contained 94.23 mass% Fe and 0.58 mass% TiO2 and showed total iron recovery of 87.62%. The latter contained 19.72 mass% Fe and 25.47 mass% TiO2, thereby providing prerequisites for titanium recycling.
{"title":"Recovering titanium and iron by co-reduction roasting of seaside titanomagnetite and blast furnace dust","authors":"Tianyang Hu, Tichang Sun, Jue Kou, Chao Geng, Xiaoping Wang, Chao Chen","doi":"10.1016/j.minpro.2017.06.003","DOIUrl":"10.1016/j.minpro.2017.06.003","url":null,"abstract":"<div><p><span><span>Co-reduction roasting of seaside titanomagnetite<span> and blast furnace dust was investigated to maximize the use of these ores in Indonesia. This direct reduction process utilizes fixed carbon in BFD to reduce iron from BFD and titanomagnetite. X-ray diffraction and X-ray fluorescence analyses were performed to characterize the reduced iron powder. The influences of reduction conditions, such as reduction temperature and duration, C/Fe molar ratio, grinding fineness and </span></span>fluorite dose, on the indicators of reduced iron powder were evaluated. Fixed carbon and volatile matter contents were lower in BFD than those in coal. However, reduction and separation of titanium and iron exhibited similar effects on reduction roasting. Results showed that the optimum conditions of roasting reduction included C/Fe molar ratio of 0.65, fluorite dose of 4</span> <!-->mass%, and roasting temperature of 1300<!--> <!-->°C for 60<!--> <!-->min. The reduced iron powder was obtained through two-stage grinding and two-stage magnetic separation of the roasted product. The former contained 94.23<!--> <!-->mass% Fe and 0.58<!--> <!-->mass% TiO<sub>2</sub> and showed total iron recovery of 87.62%. The latter contained 19.72<!--> <!-->mass% Fe and 25.47<!--> <!-->mass% TiO<sub>2</sub>, thereby providing prerequisites for titanium recycling.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.06.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42758354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-08-10DOI: 10.1016/j.minpro.2017.05.011
Mario Menéndez, Malcolm Gent, Susana Torno, Nerea Crespo
Ball mill charge size distributions originally specified for Bond grindability tests to determine the Bond Work index (BWi) are not commercially available. Those proposed to date do not match all of Bond's (1961) original specifications of total ball mass, number and surface area. An alternative mill ball charge is proposed that closely approximates Bond's original total ball mass, number of balls and ball surface area.
Results of 30 Bond Work index tests of six pure materials (calcite, magnesite, labradorite (feldspar), quartz, andalusite and glass) using closing screen apertures (P1) values of 500, 250, 125, 90 and 63 μm are analysed. The samples were selected on the basis of having distinct hardness's (Mohs hardness 3 to 7.5), being relatively free of crystallographic defects and having distinct cleavage properties The 80 percentile size of the fines produced (P80) concur with those of published values.
The trend based of P80 values for P1 values of 150 to 44 μm recommended by Bond poorly fit with published P1 values > 250 μm. It is demonstrated that the BWi test P1 values of mono-mineralogical or mono-material samples determines the P80 value obtained. Based on test results of this investigation a polynomial exponential equation relating P80 to P1 values with an R2 correlation factor of 0.9977 is presented. This relation is independent of the tested material hardness and crystallographic defects and planes of weakness.
{"title":"A Bond Work index mill ball charge and closing screen product size distributions for grinding crystalline grains","authors":"Mario Menéndez, Malcolm Gent, Susana Torno, Nerea Crespo","doi":"10.1016/j.minpro.2017.05.011","DOIUrl":"10.1016/j.minpro.2017.05.011","url":null,"abstract":"<div><p>Ball mill charge size distributions originally specified for Bond grindability tests to determine the Bond Work index (BWi) are not commercially available. Those proposed to date do not match all of Bond's (1961) original specifications of total ball mass, number and surface area. An alternative mill ball charge is proposed that closely approximates Bond's original total ball mass, number of balls and ball surface area.</p><p><span>Results of 30 Bond Work index tests of six pure materials (calcite, magnesite, labradorite<span> (feldspar), quartz, andalusite and glass) using closing screen apertures (P</span></span><sub>1</sub>) values of 500, 250, 125, 90 and 63<!--> <!-->μm are analysed. The samples were selected on the basis of having distinct hardness's (Mohs hardness 3 to 7.5), being relatively free of crystallographic defects and having distinct cleavage properties The 80 percentile size of the fines produced (P<sub>80</sub>) concur with those of published values.</p><p>The trend based of P<sub>80</sub> values for P<sub>1</sub> values of 150 to 44<!--> <!-->μm recommended by Bond poorly fit with published P<sub>1</sub> values ><!--> <!-->250<!--> <!-->μm. It is demonstrated that the BWi test P<sub>1</sub> values of mono-mineralogical or mono-material samples determines the P<sub>80</sub> value obtained. Based on test results of this investigation a polynomial exponential equation relating P<sub>80</sub> to P<sub>1</sub> values with an R<sup>2</sup> correlation factor of 0.9977 is presented. This relation is independent of the tested material hardness and crystallographic defects and planes of weakness.</p></div>","PeriodicalId":14022,"journal":{"name":"International Journal of Mineral Processing","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.minpro.2017.05.011","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48056787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}