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By Herman Mendoza, Luisa Ciriaco

An investigation of the seeding mechanism using heterocoagulation and the Derjaguin - Landau - Verwey - Overbeek (DLVO) theory of two pure minerals is the objective of this study. The seed was silica with modal diameters of 4.529 µm (fine particles) and 5.216 µm (coarse particles) and the test powder was hematite with a modal diameter of 0.883 µm. Parameters included variations in the concentration and particle size of silica. Both particles were first subjected to size determination and settling tests via Stoke’s Law. The silica-hematite system was then suspended in 0.001 M KNO3 electrolyte solutions where pH was adjusted. Afterward, the suspension was agitated and was allowed to settle at different time intervals while obtaining turbidity readings. Results through settling time and turbidity vs. pH graphs indicate that maximum heterocoagulation occurs from pH 2 to 5 while minimum heterocoagulation occurs from pH 6 to 7. At these pH levels the zeta potentials of silica and hematite are negative and positive, respectively. On the contrary, repulsive forces dominate the system from pH 8 to 11 due to the particles’ negative zeta potentials. Furthermore, the attachment of hematite to silica increases when the parameters become larger thereby increasing the effectivity of heterocoagulation at acidic to neutral pH levels.

Jan 1, 2014

By X. L. Song

In this paper, ZrSiO4-Cd(S1-xSex) inclusion pigments were synthesized by hydrothermal method. Microstructure, morphology and properties of the powder were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), infrared spectroscopy (IR) and CIE chromaticity, respectively. It shows that, precursors obtained at pH is about 6.0 are sol and products with higher crystallinity, red hues (a*=38.23) and inclusion ratio when hydrothermal synthesis temperature is 180? and holding time is 12h. Hydrothermal reaction mechanism was further analyzed as well. In particular, an ideal model of pigment formation was proposed.

Jan 1, 2014

By Ming’an Wei, Chuanyao Sun, Zhenguo Song, Zengwen Dou, Yangge Zhu

"The effects of pH value and dissolved oxygen(DO) in the pulp to the Eh and flotation recovery of pyrite were investigated using potential online detection system. The effects of DO on the Eh and flotation recovery were tested which DO changed from 0.5mg/L to 19.5mg/L in six different pH buffer flotation systems (pH: 4.00, 5.62, 6.86, 9.18, 10.01 and 10.96 respectively). Results of potential detected online demonstrated that the pyrite electrode has nearly the same response to potential as with platinum electrode for the FeS2-xanthate-H2O flotation system under the study conditions. Pulp potential and recovery of pyrite were remarkably influenced by pH, both of them decreased with the increasing of pH and, especially, sharp decreased after pH above 9. As the concentration of DO was increased, the Eh was also increased in all the six different buffer solution, while the flotation recovery was decreased. And the amplitude of variation for Eh was not obvious in acidic and neutral solutions, but on the contrary, the change for flotation recovery was remarkable in neutral and alkaline conditions. This may indicate that the flotation of pyrite will be deteriorated in alkaline and high DO concentration conditions."

Jan 1, 2014

By John A. Rumball, Martin R. Houchin

"For gold leaching of oxide ores, the optimum cyanide : oxygen ratio is approximately 106 mg/L NaCN : 10 mg/L O2 (6.9:1 by mole). In sulphide ores, galvanic coupling of the gold with the electrically conductive sulphides significantly increases this ratio such that leaching may occur in a relatively low dissolved oxygen (DO) environment.RESULTS AND DISCUSSIONGold leaching in a carbon in pulp (CIP) and carbon in leach (CIL) circuit is driven by the supply of cyanide and oxygen, as described by Elsner’s equation (1):• 4Au + 8CN- + O2 + 2H2O ? 4Au(CN)2 - + 4OH- (1)Equation 1 suggests that the ideal molar cyanide : oxygen ratio should be 8:1, or 122.5 mg/L NaCN to 10 mg/L of DO. It is generally accepted however, that oxygen is not completely reduced to hydroxide at the gold surface, and that equation (2) better represents the gold leaching reaction (Marsden and House, 1992):• 4Au + 8CN- + 2O2 + H2O ? 4Au(CN)2 - + 2OH- + H2O2 (2)Additionally, since gold leaching is limited by either the diffusion of cyanide or oxygen to the gold surface (Habashi, 1993), then the relative diffusion rates of cyanide and oxygen must also be taken into account. Marsden and House (1992) suggest that the ideal molar cyanide : oxygen ratio is 6:1, while a more recent investigation using laboratory and plant observations (Heath and Rumball, 1998) suggested a molar ratio of 6.9:1.In practice, although a cyanide : oxygen mole ratio of 6.9:1 applies to some circuits, there are many instances when this is not the case.In sulphide ores, galvanic coupling of the gold with the electrically conductive sulphides significantly increases this ratio. Galvanically connected sulphides, and possibly carbon, provide a large surface area for oxygen reduction. As the cathode surface area increases, the oxygen concentration required to sustain the same rate of gold oxidation decreases proportionately.Galvanically connected particles may be composite particles, however they may simply be liberated sulphides in the same suspension as the gold. Particle collisions within a slurry are sufficient to provide momentary galvanic connection (Greet, 1995)."

Jan 1, 2003

By H. D. Mendoza, M. J. C. Zerna

This study aims to determine the stability of Philippine nickel laterite ore by investigating the behavior of fine minerals of silica (dave=1.514 µm), hematite (dave= 0 1.351 µm), and nickel oxide (dave=1.426 µm) and their mixed-components in dilute aqueous suspension as a function of pH and electrolyte concentration. The zeta- potentials of the minerals are measured and stabilities of different component systems in aqueous suspension are determined. Hamaker constants of the minerals in aqueous medium are derived by getting their respective critical coagulation concentrations (c.c.c.) at stable pH conditions and at various concentrations of KNO3. The iso-electric points (i.e.p) for silica, hematite, and nickel oxide particles are at pH 2, pH 7.5, and pH 8.5, respectively. The stability behaviors of component systems are as follows: a) Silica dispersion is stable at pH range 3-11and unstable at pH 2; b) Hematite dispersion is stable at pH 2-5 and pH 8-11, and unstable near pH 7; c) Nickel oxide dispersion is stable at pH range 10-11 and unstable at pH 3-9; d) Hematite-silica dispersion is stable at pH range 6-11 and unstable at pH range 3-5; e) Hematite-nickel oxide dispersion is slightly stable at pH range 3-4 and unstable at pH range 5-11; f) Silica-nickel oxide dispersion is stable at pH range 10-11 and unstable at pH range 3-9; and, g) Hematite-silica-nickel oxide dispersion is stable at pH range 10-11 and unstable at pH range 3-9. The stability of nickel laterite ore is similar to that of the three-component system in an aqueous environment. The stability tests are analyzed using the classical DLVO theory. The stability conditions in an aqueous environment are essential in developing the appropriate process flow for the separation/ recovery of nickel laterite mineral components and also in the treatment of nickel laterite -laden wastewaters.

Jan 1, 2018

By de Vaux. D.

Synthetic water with a calcium concentration of 80 ppm and 500 ppm was prepared and the flotation results obtained compared to a simple electrolyte in order to determine the effect water quality has on pentlandite and pyroxene surface alteration and, ultimately, floatability. During the study, the possible effect of interactions between the minerals investigated and Ca2+ ions in the presence of sodium isobutyl xanthate was studied at pH 6 and pH 9 by means of zeta potential determinations, microflotation tests and ToF-SIMS analysis. The results obtained have demonstrated that water quality does play a significant role in flotation recovery at the experimental conditions used.

Jan 1, 2003

By Gerke Gilian, Pretz Thomas, Pehlken Alexandra

"The evaluation of health hazards within the treatment of mineral and waste materials is gaining more and more importance in industrial countries. The need to control occupational health and safety has been recognised, and regulations which describe general protective measurements for personnel provide a tool to protect their health. It is the aim of the paper to give an outlook for practical approaches to risk assessment and to present measures for exposure reduction in accordance with the state of the art in Germany.Both the treatment of minerals and of waste materials are described in relation to the risk assessment. The method of evaluating health hazards in the two industries is similar and therefore both examples are presented next to each other.The example presented in the paper is the German “Biostoffverordnung” (the regulation for biological materials) which is important for the waste treatment industry. All kinds of waste treatment facilities (like composting facilities, waste dumps, sorting facilities for packaging materials) are obliged to carry out an assessment of health hazards for a variety of working areas and working places. The possible safety requirements deriving from this regulation are presented and discussed under the aspect of biological hazards."

Jan 1, 2003

By A. Yörükoglu

In this study, thorium mineral that found in the complex ore deposit bearing bastnasite, fluorite, and barite from Eskisehir - Sivrihisar district has been tried to extract by using HCl and H2SO4 leaching. Ore sample of approximately 3 tons taken from the ore deposit has been homogenized in order to obtain composite samples by means of ore preparation techniques for experiments. Results of chemical analyses of composite samples are as given; 40.8% CaF2, 35.35% BaSO4, 2.01 Ce, 1.5% La, 0.39% and 0.1% Th. HCl and H2SO4 leaching processes have been performed to gain Th in the ore. For determining the optimum particle size, the samples have been ground under controlled conditions and brought to the sizes of 0.065, 0.2, 1 and 3 mm. Leaching experiments have been carried out in both HCl and H2SO4 acids without roasting and roasting at the temperature of 900°C for 1, 3 and 6 h retention times for all particle sizes determined before. In the experiments, the highest Th recoveries reached are as follows; 78.74% Th when H2SO4 and 1 mm particle sized sample used, and 1 h roasting applied and 73.38% Th when HCl and 1 mm particle sized sample used, and 3 h roasting applied. Keywords: thorium, leaching, concentration, sivrihisar, roasting

Sep 1, 2012

The flotation behavior of kaolinite and diaspore using N, N-diethyl dodecyl amine (DEN12) and N, N-dimethyl dodecyl amine (DRN12) as collector have been investigated through flotation experiments. The mechanism of adsorption of two tertiary amine collectors on surface of kaolinite and diaspore were investigated by FTIR spectral, Zeta potentials measurements and calculation of molecular orbital energy. It has been found that DEN12 and DRN12 have stronger collecting power to kaolinite and weaker collecting abilityto diaspore than DDA. Kaolinite and diaspore in bauxite ores can be separated by using DEN12 and DRN12 as collectors at pulp pH below 8 and 6, respectively. The results of zeta potentials and calculation of molecular orbital energy indicated that the adsorption strength on kaolinite surface is in the order DEN12>DRN12>DDA and the adsorption strength on diaspore surface is in the order DDA>DEN12>DRN12. FTIR spectral analysis and Zeta potentials approve that the action between kaolinite and tertiary amine collector is strong electrostatic adsorption and that of diaspore is weak electrostatic adsorption in the range of pH 5~6.

Jan 1, 2014

By H. Kasaini

Batch wise adsorption tests for platinum (Pt) on the surface of activated carbon pellets (Norit RO 0.8 BET surface area 1100 mg/g) were carried out in mixed chloride solution. The purpose of this study was to assess and compare the adsorption performance of amine-treated activated carbons (AACs) and native activated carbons (NACs) in terms of adsorption capacity and selectivity. The effect of pH and temperature on adsorption capacity and selectivity was established. The amine- treated ACs were prepared by anchoring the amino groups (butyl amines) on the surface of AC pellets in aqueous media and the UV-Vis was used to determine the amount of amine sequestered from solution by ACs. The dosage of butyl amine on the surface of ACs averaged 0.15 g/g, carbon. The adsorption mechanism was described by the ionization and complexation model whereby interaction between the protonated AAC surface and the anionic chlorocomplex ions (PtCl5 [H2O]-, PtCl62-) proceeded by either electrostatic attraction or/and by covalent bonding [(NH3)2PtCl6 or (CH2COO)2PtCl6]. By comparison, the adsorption capacities of Pt on amine-treated ACs and native ACs were 53.8 mg/g and 33.03 mg/g, respectively which highlight the benefits of anchoring functional molecules on ACs. The selectivity of AACs was influenced by solution pH. Pt adsorbed selectively on the surface of amine-treated ACs at pH<1.5. The highest separation factor that was recoded pertained to Pt and Fe species (ßPt/Fe = 90) then followed by Pt and Ni species (ßPt/Ni = 30) or Pt and Cu species (ßPt/Cu = 15). The lowest separation factor was recorded for Pt and Cr ions (ßPt/N= 5). Adsorption kinetics of Pt on amine-treated AC surfaces, according to the first and second order reactions, were investigated and results showed that rates were in the order 10= 5). -4 min-1 and 102 g?min/mg, respectively. The pseudo 1st order kinetics predicted the adsorption capacity of 51.81 mg/g which was almost similar to the experimental value (53.8 mg/g) while the second order rate equation predicted Pt adsorption capacity of 40.1 mg/g. Both The Langmuir and Toth isotherm fitted the Pt adsorption at pH < 1.0. The Freundlich isotherm tended to underestimate the adsorption capacity of AACs.

Jan 1, 2014

By M. F. He

There are three polymorphic modifications in pyrrhotite (monoclinic, hexagonal and orthorhombic), with monoclinic and hexagonal polymorph being more abundant. The floatability of different crystalline structures of pyrrhotite (monoclinic and hexagonal) is studied in this paper. It is shown that the floatability difference of monoclinic and hexagonal is obvious and that the flotation recovery of monoclinic pyrrhotite is greater than that of hexagonal pyrrhotite using different collectors . Using butyl dithiophosphate as collector, the flotation recovery of pyrrhotite is higher than when sodium diethyl dithiocarbamate and sodium butyl xanthate are used as the collectors. Monoclinic and hexagonal pyrrhotites are more easily activated by Cu2+ in acidic conditions than in alkaline conditions, while Cu2+ can not activate hexagonal pyrrhotite when sodium diethyldithiocarbamate was used as the collector. By the measurement of contact angle, it is indicated that monoclinic and hex-agonal pyrrhotite float well and are easily activated by Cu2+when dithiophosphate was used as the collector. Using sodium diethyl dithiocarbamate as a collector, the flotation behavior of pyrrhotite was investigated. The relationship between potential and pH range for pyrrhotite flotation was established. The results show that the flotation of pyrrhotite is dependent on pulp potential at certain pH values.

Jan 1, 2014

By K. S. McClure, S. B. Chitralekha, R. B. Gopaluni, Chmylek. T., S. L. Shah

This is a tutorial paper on industrially successful approaches for nonlinear process monitoring. Online process monitoring is essential to continuous operation of plants at high efficiency. The problem of process monitoring is one where an impending but undesirable process condition has to be identified and used to alert process engineers. This problem has traditionally been solved by practicing engineers using statistical techniques that detect a change in the underlying correlation structure of process variables. For linear correlation structures, algorithms such as principal components analysis, independent component analysis and partial least squares have been proposed. However, many industrial processes exhibit nonlinear correlation structure between the process variables. In this tutorial we describe various nonlinear monitoring techniques and elaborate on two recently developed methods, namely Support Vector Machine and Local Linear Embedding. The two methods are evaluated by application on two experimental case studies, a SAG mill and a polymer extruder.

Jan 1, 2014

By S. Castro, L. Uribe

Seawater can be considered as a particular process water with a high concentration of NaCl (about 0.5- 0.6 mole/L) and high concentration of hydrolyzing metal cations (mainly, Mg2+ and Ca2+ ions). Micro-flotation tests, induction time measurements, and zeta potential measurements have been used to investigate the effect of these ions on the natural floatability of molybdenite. The results demonstrate that molybdenite is strongly depressed in the alkaline pH range over which hydrolysis products of Mg2+ and Ca2+ ions are formed. At pH 10, colloidal magnesium hydroxide seems to be responsible for molybdenite depression in seawater and in Mg2+ solutions. This is also supported by the measurements of the effect of Mg2+ ions on the zeta potential of molybdenite. The mechanism of depression of molybdenite with Ca2+ ions is different, and depression takes place in the pH range were Ca(OH)+ complexes are formed, below the pH of precipitation of calcium hydroxide. Adsorption of the cationic hydroxy species and/or hetero-coagulation of the positive charged colloidal hydroxide on the negative charged molybdenite particles seem to be the main mechanisms involved.

Jan 1, 2014

By D. DePaoli, P. Zhang

"Phosphate ore is one of the most significant secondary resources for rare earth elements (REEs), and Florida phosphate is of particular interest due to its much higher ratio of heavy REEs, especially yttrium. Analyses of numerous samples from different phosphate processing streams in Florida showed that heavy REEs account for about 50% of the total REEs in Florida phosphate with yttrium accounting for approximately 30%. It was estimated that the amount of yttrium from US phosphate processing could meet the world demand for this critical element. This research aimed at recovering both REEs and phosphorus from a phosphate flotation tails. This tails is composed of mainly silica and phosphate with a small fraction of heavy minerals including monazite and xenotime. Since the specific gravity of silica is 2.6 versus 3.2 for phosphate and 4.5-5 for rare earth minerals, pre-concentration of the minerals of interest by gravity separation was investigated first. A pilot scale shaking table was used in this study. One pass gravity concentration achieved a shaking table concentrate analyzing over 600 ppm REEs at about 40% recovery. Flotation of the shaking table concentrate resulted in a product containing 1809 ppm REEs and 26.37% P2O5 with corresponding recoveries of 73% and 82%. Sulfuric acid leaching at 75oC could recover over 60% REE and nearly all the P2O5. Higher REEs (>90%) recovery was achieved by conducting leaching at higher temperature with concentrated sulfuric acid. The phosphoric acid from leaching of the flotation concentrate is of superior quality compared with that generated from regular phosphate rock.INTRODUCTION Rare earths are a group of 17 elements including those of the lanthanum series, as well as the non-lanthanides, yttrium and scandium. These elements have very specific critical uses in a multitude of markets. For example, lanthanum is used as a catalyst in breaking down crude oil to produce gasoline, diesel and jet fuel and neodymium is the core magnetic component in high-strength magnets for electric car batteries, wind turbines and hard disk drives. Rare earths are also essential for many military applications. Many of these applications have no substitute materials and the move to green technologies has dramatically increased their demand."

Jan 1, 2018

"The JKMRC researchers have been redeveloping the suite of breakage testing techniques to more realistically align with the breakage environment in comminution equipment. Computational modelling, especially with the DEM, has highlighted the modes of impact and contact, along with the energies of these interactions in a wide range of equipment. This has driven the need to match these modes in laboratory ore characterisation tests. The objective has been to build a continuum of breakage tests and associated models that span the required range of breakage forces and environments. The ore sample is subjected to a sequence of tests covering: abrasion (surface breakage) of angular through to smoothed particles; single particle impact from high energy single impact breakage down to low energy; incremental breakage covering 60 mm down to 50 µm particles; particle strength distribution; and bed breakage over a range of compression and energy input. These tests are suited to multi-component ores with a distribution of strengths. A modelling technique is also being developed to utilise primary breakage for modelling breakage under different types of confinement. This paper draws together these techniques, previously published by the authors, into a coherent whole. The suite of tests is approaching the point where a fixed set of tests can be used to model the performance of a full range of equipment, removing the need to conduct repeat ore characterisation tests for each different piece of equipment incorporated in a circuit design. This path should open up the application of different circuit configurations and novel equipment in comminution circuit design.1 INTRODUCTION Comminution modelling utilizes a wide range of ore characterisation techniques and methods to deal with the range of comminution equipment available for production use. In general, the tests have been designed to correlate with specific pieces of equipment, using calibration factors to provide the link between the small-scale test and industrial-scale performance. The majority of tests focus on estimating the power requirement of process equipment to achieve a desired throughput and grind size. Overall, this approach has achieved acceptable outcomes in the past, but the reality is that equipment sizing suffers from considerable uncertainty, in excess of ±20% is not uncommon. This uncertainty is covered by safety margins and automatic scaling factors in equipment selection. In striving to improve reliability, the industry tends to add more adjustment factors to the tests, and design margin rather than question the basic validity of the testing process. As the tests are often correlated to production equipment via carefully guarded databases, they are also locked into historic operating inefficiency, not providing direction or revealing opportunities to improve production efficiency in comminution equipment or circuits. Safe in the knowledge that they are achieving the expected production based on test work predictions, a site is unlikely to set their sights on reducing specific energy consumption by 10%."

Jan 1, 2018

By Y. S. Song

Flotation separation of galena, sphalerite with pyrrhotite in ethanoic acid + sodium acetate sys-tem was studied in this paper. The flotation tests show that galena and sphalerite can float but pyr-rhotite can hardly float in the pH range of 3.6 to 5.6 in ethanoic acid + sodium acetate system. The flotation tests also show that galena can be separated efficiently from pyrrhotite and sphalerite can be separated on the whole from pyrrhotite, but the separation efficiency of the former is much better than the latter. The flotation results have been investigated by ultraviolet spectrum and XPS analysis, and explained by theory of hard and soft acid and base (HSAB), hydrogen bond and galvanic coupling.

Jan 1, 2014

By S. Castro

Molybdenite flotation is strongly depressed at pH higher than 9.5 in the flotation of Cu-Mo ores in sea water. Chemically sea water contains mainly Na+ and Cl- ions, but also some secondary ions, such as SO42-, Mg2+; Ca2+, HCO3-; etc., which are not necessarily indifferent for the flotation of molybdenite. The natural floatability of molybdenite in sea water and in NaCl solutions containing different secondary ions is investigated by micro-flotation tests. The tests indicate that the floatability of molybdenite in alkaline media in 0.6 M NaCl solutions is not affected by the presence of anions, such as, SO42- and HCO3-, at concentrations similar to those occurring in sea water. However, a strong depression of molybdenite at pH ranging from 9.5-10.0, is produced by the alkaline earth metal cations (Ca2+ and Mg2+ ions), dissolved in distilled water or in 0.6M NaCl solutions. It was found that effect of Mg2+ions is significantly stronger than Ca2+ ions. Effect of both ions is attributed to hydrolysis and adsorption of MOH+ hydroxy-complexes. This is followed by subsequent precipitation of hydrophilic colloidal hydroxides at the molybdenite/solution interface, and in bulk solution.

Sep 1, 2012

By Georg Unland, Thomas Wegner

"Different types of impact crushers use the physical effect of impact to crush rocks. The rocks can vary from soft to hard and from ductile to brittle but they should never be abrasive. Since the principles of impact crushing of larger rocks are hardly investigated these crushers are still sized rather by empirical than by scientific approaches.In order to investigate the principles of comminution by impact of large rocks a test rotor was developed and rocks of different dimensions were tested. The integrated measuring devices of the rotor enable the recording of impact forces and of absorbed impact energy with high resolution during the contact time.Since impact crushers stress the rock particles with a defined velocity the main crushing properties are gained as a function of the applied velocity and the particle size of the rock: likelihood of breakage, contact time, maximum crushing force, mass specific crushing work, surface related crushing ratio and crushed fragment shape distribution."

Jan 1, 2003

By E. Lee

With the growing environmental concern, as well as the increasing concern for sustainability of natural resources, the need of improving the performance and efficiency of today?s crushers is be-coming increasingly important. However, the development of existing crushers requires an extended basic knowledge about the crushing process itself. The aim of the present study is therefore to find the theoretically optimal way of crushing compressively under given circumstances. In the present paper, optimizations have been performed with the purposes of maximizing product yield and minimizing energy consumption. Performed on an ideal crushing stage free from physical limitations, the optimization results have been obtained in terms of number of compressions and their corresponding compression ratios. Complementing earlier results on interparticle breakage (Hulthén et al., 2006), presented here are thus the results from corresponding optimizations with single particle breakage and interparticle breakage. It is concluded that modern crushers are not working optimally in any of the studied aspects for gneiss. In fact, optimizations indicate that a lowering of the compression ratio, as well as a shortening of the crushing sequence, are theoretically favourable. The outcome of this study is therefore highly promising as to giving new ideas and suggestions of improvements in existing crushers, and can even result in redesign of compression crushers.

Jan 1, 2014

By Wei Sun, Xue-feng Cao, Lei Sun, Run-qing Liu

The flotation performance of kaolinite in laboratory micro-flotation was investigated with 3- (dodecyloxy) propan-1-amine (ON12) as the collector. Compared with dode cylamine (DDA), which is commonly used as the bauxite reverse flotation collector, ON12 shows stronger collecting ability for kaolinite than using the same amounts of DDA, when experimental pH value reaches more than 6. With the addition of ON12, the isoelectric point of kaolinite shifts to 6.1 from 3.6, which suggests a strong adsorption between kaolinite and ON12. Infrared spectra analysis indicates that the type of ON12 adsorbed on the kaolinite surface is mainly of electrostatic adsorption. Molecular dynamics simulation further indicate that electrostatic adsorption of ON12 cation on kaolinite (001) surface based on electrostatic interaction between NH4+ and O atoms. ON12 will be suitable for bauxite reverse flotation with the efficiency depressors of the diaspora.

Jan 1, 2014