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By C. H. Veloso

"Starch is the most widely used depressant in the reverse cationic flotation of iron ores. There is however, an indication from recent studies, that other polysaccharides may successfully replace them. When starches are used in the flotation of iron ores in the presence of quartz as gangue mineral, their strong adsorption on the surface of iron oxides can be explained by the molecular conformation between the available sites on the mineral surface and two hydroxyls of starches. However, when the gangue minerals are iron-bearing silicates, the strong interaction with starch can occur on these minerals since they have the same surface behaviour as iron oxide. In this work bench scale tests were conducted in order to generate scientific knowledge about other alternatives depressants for the flotation of iron ores. A magnetic pre-concentrate from a skarn iron ore processing plant was used as feed material for flotation tests. The reverse flotation approach was used to upgrade the iron content by removing complex ironbearing silicates. The depressants used in this study were: corn starch, dextrin, carboxymethyl cellulose (CMC) and humic acid. The tests were performed under different pH conditions in order to try to relate the efficiency of depression to the pH used during flotation. The results show the important role of pH as each depressant reached its best performance at different pH values. At alkaline pH the corn starch showed best depression performance while the humic acid is more efficient at pH close to neutrality.INTRODUCTIONIron corresponds to approximately 6% of earth’s crust composition (McDonough and Sun, 1995). It is the most used metal in our lives, some of its properties as resistance and facility to be shaped makes is replacement very difficult. The primary sources of iron on our planet are minerals. The iron-bearing minerals most commonly found in nature and economically exploited are magnetite [Fe3O4], hematite [Fe2O3], goethite [FeO(OH)] and siderite [FeCO3] (L O Filippov et al., 2014). These minerals are commonly associated with other minerals (most of the time not economically exploited) forming the so-called iron ore. Iron ore is the source of primary iron for the world’s iron and steel industries."

Jan 1, 2018

By V. D. Tathavadkar

Natural chromite mineral is a solid solution of spinet end members namely: chromite (FeCr2O4), hercynite (FeA1204), magnetite (Fe3O4), magnesio-chromite (MgCr2O4), (MgA12O4), and magnesio-ferrite (MgFe2O4). A phase transformation in chromite minerals occurs in oxidising conditions during the soda-ash roasting reaction. This phase transformation plays an important role in improving the extraction efficiency of Cr3+ from mineral phase. The extraction efficiency of chromium (Cr3+) from chromite to a water¬soluble sodium chromate (Cr6+) salt depends upon the decomposition kinetics of the spinet phase. An investigation of the phase changes in chromite ores in the absence of sodium carbonate was carried out in air, argon, and in argon +5 % hydrogen gas mixture. The thermodynamics of phase transformation reaction in chromite solid solution phase is discussed using the solution model proposed by Sack and Ghiorso [1]. The microstructural changes and the changes in elemental compositions of different phases were examined by SEM and electron probe microanalysis (EPMA) respectively. The experimental results indicate that the solid solution spinet phase in chromite mineral undergoes spinodal decomposition under the influence of oxygen partial pressure and temperatures. The structure of phases formed and their morphologies suggest that the phase decomposition may be similar to those observed by Burkert et. a]. 121, although the scale of phase separation in chromite appears to be strongly dependent on oxygen partial pressure.

Jan 1, 2001

By R. T. ROLFE

IN this critical age, people are not content .with the judgments passed on men and things long ago, but must needs revise them. It is an excellent spirit, so long as we do not start out with the idea that old opinions must necessarily be wrong, and that all ancient malefactors must therefore be whitewashed. That interesting ogre, Gilles de Retz, to whom the process has recently been applied, is no longer with us, so no one will be the worse for it, but the old bugbear8 of the steelmaker, sulfur and phosphorus, still are, and now Mr. McIntosh, in a recent article in these pages, asks us to regard one of them in a new light.' This article is a most interesting one, with much of which one must agree. One of his -statements, how- ever, although correct, is somewhat' misleading, and he rather discounts the fundamental objection of the steelmaker to phosphorus, its dangerous propensity to segregate and the secondary effect on the carbon distribution and therefore on the homogeneity of the steel that is produced thereby. Further, the evidence on which he bases his claim that phosphorus does not lower the impact strength of steel is rather slight. The writer views with the utmost misgiving any proposal to increase the amount of phosphorus in steel, and cannot regard it in any other light than as a prejudicial impurity, to be kept down to as low a proportion as possible. It thus becomes necessary to examine the evidence upon which Mr. McIntosh's claims are based

Jan 1, 1926

By Blake M. Loring, Robert A. Colton

MELTING procedures for most metals and alloys usually include some provision for the control of oxygen, since this element frequently has some undesirable effect on the properties of the metal or alloy concerned. In the melting of the various bronzes, this is especially true, since oxygen can be introduced into the melt in a number of ways, most of which are difficult to control. In making bronzes from virgin materials, oxygen is usually present in the commercial grades of copper used; electrolytic he refined copper ingots usually contain from 0.02 to 0.05 per cent oxygen. When ingot metal or scrap bronze is used in the charge, oxides are almost always present to some degree. Under certain melting conditions and in certain types of melting equipment the atmosphere over the metal may be highly oxidizing. This, of course, may be desirable in the melting practice used, but is certain to introduce appreciable amounts of oxygen into the melt, and that may not be entirely desirable. From the foundry viewpoint oxygen may have several harmful effects on bronzes. The formation of excessive amounts of oxides may produce drossy metal, which, in turn, means dirty castings and a potentially high rejection rate. It is claimed, too, that oxides in the metal may combine with hydrogen to form steam and thereby produce porosity in certain of the bronzes. The presence of certain refractory oxides, such as SnO2, may be undesirable from the viewpoint of making machining difficult, or as possible stress-raisers in the metal matrix. It is often said that excessive oxide present in the liquid metal makes the metal run sluggishly. Since it appears impractical to try to control the amount of oxygen introduced into the metal beyond taking the economical limit of precaution about charging dirty scrap, it would seem that control of the oxygen content of the liquid metal offers the most promising approach to this problem. This might be done by using slags, or covers, or by the use of some element or compound added to the melt to remove oxygen preferentially. Most aspects of this problem have been considered and considerable work has been done along these lines. A reconsideration of the problem is indicated, however, by the controversial nature of the evidence at hand, especially on the possibility of using a chemical deoxidizer to control the oxygen content of bronzes. CHOICE OF DEOXIDIZER The choice of the chemical agent selected as a deoxidizer would naturally depend first on the alloy in which it is to be used; in this particular case the alloy is Navy gun metal. In Table I are listed a group of elements that might be considered as

Jan 1, 1946

By E. M. Abraham

The establishment and survival of different grass species and cultivars on various phytotechnic treatments at a limestone quarry was studied. The treatments applied were: a) bare soil, b) bentonite, c) bentonite-straw and d) asphalt-straw. According to the results, significant differences were found among species and cultivars, growing on different treatments as far as plant growth and survival are concerned. The seed germination was higher on bentonite -straw and asphaltic-straw than on bentonite but the plants survival were higher on bentonite. Lolium perenne had higher seed germination rate and better establishment than the other tested species at all treatments. However, the survival rate of Agropyron desertorum and of the cultivars palestina and chrysopigi of Dactylis glomerata was higher than of the other species.

Jan 1, 2007

By E. Saari, B. Musuku, K. Jansson

The quality of the concentrator plant process water is crucial for high performing mineral flotation circuits. Significant metal recovery and concentrate grade losses have been noticed particularly in more closed water loops. The recovery and quality losses have started to emerge mainly with decreased freshwater usage and because of changes in tailings management towards tailings thickening, paste, or dry stacking. These changes result in shorter, closed water loops with a rapid build-up of harmful components with negative impact on the beneficiation process. Consequently, water quality has a direct link to decreased product value and sales returns. Complete cleaning or water blending might not be the right way to achieve high recovery and high-quality products. Instead, the key is to understand what kind of water qualities are needed for the flotation of specific minerals. In this study harmful substances in various plant water streams were removed and/or modified by pilot-scale dissolved air flotation. Batch-scale mineral flotation tests with the untreated and treated water were then performed by using fresh ore samples and the plant’s own laboratory flotation procedure. The results indicate that because of dissolved air flotation, the mineral flotation recoveries were enhanced by 1‒3.3%. Keywords: Mineral recovery, metal recovery, mineral quality, process water, concentrator, beneficiation, mineral processing, flotation, process water treatment

Jan 1, 2020

By J. Lu, J. B. Wiskel, D. G. Ivey, E. Niemi, H. Henein

Simulated TMCP using a Gleeble was undertaken to evaluate the effect of the austenite to ferrite cooling rate, coiling temperatures of either 400°C or 500°C and the magnitude of plastic deformation at the coiling temperature on the hardness of a Grade 483 (X70) steel. For comparable apparent cooling rates and deformation conditions, the hardness of the samples were independent of coiling temperature The application of a minimum compressive deformation > 8% was required to increase hardness at both simulated coiling temperatures of 400°C and 500°C. An increase in hardness was also observed with increased cooling times between 800°C and 500°C (i.e., slower cooling rates).

Jan 1, 2005

By William Ewing

Copper is rapidly being adopted by the semiconductor industry as the interconnect material of choice. The aqueous processing techniques used generate wastes such as spent electrolyte from electroplating, electroplating rinse water, copper solutions from removing copper from the back of the wafer and CMP waste streams. We are examining the use of chelating resins as a means of recovering copper from these streams within the processing plant, thereby allowing recycling of process water and minimizing hazardous waste disposal costs. We have examined the effect of model plating additives (and other organic complexing agents) on the efficacy of Dowex M4195. Although these might have had a significant effect, commonly used electroplating additives polyethylene glycol (PEG), benzotriazole (BTA), thiourea, glycine, and 3-mercapto-1-propanesulfonate (MPSA) each had little or no effect on the ability of the resin to chelate copper and remove it from solution. This suggests that Dowex M4195 could be useful for treating waste solutions of rather variable compositions.

Jan 1, 2003

By J. Gong

Fine mineral particles pose two challenging problems in froth flotation, i.e., ineffective recovery of fine hydrophobic particles and mechanical entrainment of fine hydrophilic particles. The first problem has attracted much research effort while the second problem has received much less attention. We have recently proposed a method to deal with mechanical entrainment, i.e., utilizing the flocculating power of polymeric depressants to flocculate fine gangue particles and making the flocs big enough so that the mechanical entrainment of these particles can be reduced or eliminated. In this paper, we report results on the use of polyethylene oxide (PEO) in controlling quartz gangue in the flotation of sulphide ores. PEO was found to flocculate fine quartz and lower its entrainment. It was also found to modify air/water interfacial properties and acted as a frother, which could increase gangue entrainment. Nevertheless, when used at starvation dosages, PEO was found to significantly improve the grades of the floated sulphide concentrates.

Jan 1, 2014

By Leopoldo Gutierrez, Esau Arinaitwe, Marek Pawlik

"The effect of various polymers, including: anionic carboxymethyl cellulose (CMC), polystyrene sulfonate (PSS), humic acids (HA) and non-ionic hydroxypropyl cellulose, on the wettability of Athabasca bitumen was evaluated through dynamic contact angle measurements using the captive bubble technique. The tests were carried out as a function of pH at a constant ionic strength (0.01 mol/L sodium chloride). The evolution of the three-phase contact angle between the solution, bitumen and an air bubble was followed as a function of time over a period of ~6 minutes. The contact angle data were modelled using a first-order kinetic equation. The results were analyzed in terms of the initial contact angle, the evolution rate constant, and the steady-state contact angle value. In the case of anionic polymers, a pronounced decrease in the initial contact angle value was observed at pH 3. Under acidic conditions, there was no significant effect of CMC observed on the steady-state contact angle value but PSS and HA significantly decreased the steady-state contact angle value. At pH 8.5. the anionic polymers did not affect the wettability of the bitumen surface but they significantly decreased the contact angle evolution rate. These results suggested that CMC is not capable of permanently lowering the hydrophobicity of bitumen, and the polymer only slowed down the evolution of the contact angle to the steady-state value. The results also showed that polystyrene sulfonate and humic acids were capable of making bitumen hydrophilic but only under acidic conditions. Only hydroxypropyl cellulose (HPC) produced a large decrease in the steady-state contact angle under alkaline conditions (pH 8.5). The kinetics of contact angle evolution in the presence of HPC was also drastically lowered. The results were discussed in terms of the chemical composition of the polymers and their different affinities towards the bitumen surface."

Jan 1, 2014

By J Ralston, G B. N Kaggwa, L Huynh

Three polymers of varying chemistries and molecular weights have been used to depress talc in a model sulfide ore consisting of talc, pentlandite, and chalcopyrite. Flotation testing revealed a distinct hierarchy of effectiveness of the polymers in the depression of talc (HP Starch > Polymer-H > Dextrin WY) but a different order of effectiveness for depression selectivity (Dextrin WY > Polymer-H > HP Starch). Adsorption isotherm determinations for the gangue and valuable mineral phases indicate that the differences in selectivity are partially due to adsorbed amount variations, with Dextrin WY adsorbing marginally less on the sulfides than Polymer-H. Contact angle measurements on packed particle beds have revealed that the polymers have differing abilities to reduce the contact angle of talc and the sulfide minerals. An explanation of the observed trends is given in terms of the binding mechanisms of the polymers on the talc and the sulfide mineral phases. Order of addition effects between collector and depressant were also investigated using adsorption isotherm determinations for the polymers in the presence of a pre-adsorbed layer of collector and vice versa. Adsorption of the polymers was not affected by the presence of the collector. Similar results were obtained for the adsorption of collector in the presence of pre-adsorbed layers of polymer.

Jan 1, 2005

By Eduard Ouerra, Nuo Jin

"The use of polytetrafluoroethylene, PTFE, as a solid sorbent for elemental sulfur during pressure oxidation of chalcopyrite was investigated. The effects of agitation, PTFE particle size and lingin sulfonate addition were evaluated using leaching conditions that were otherwise similar to those employed in the CESL process. The effects of these factors and their interactions on chalcopyrite oxidation are explained in terms of interfacial forces and solid-solid interactions. Using relatively fine PTFE powder with vigorous agitation resulted in about 100% copper extraction in less than 90 minutes without the need for grinding of the flotation concentrate.IntroductionThe extraction of copper from sulfide ores has always been dominated by the conventional pyrometallurgical smelting process. Though much effort has been made to develop various hydrometallurgical processing routes, smelting remains as the dominant process, treating approximately 80% of the chalcopyrite concentrates worldwide [1]. However, some of recently emerged techniques for treating chalcopyrite through hydrometallurgical routes are showing results that are competitive with smelting in terms of economical feasibility. Representative methods include: Activox Process, CESL Process, Anglo/UBC Process, High Temperature Pressure Oxidation, and Bio-Oxidation. Among these, the CESL processes operate at a medium temperature range (typically 140-150GC) and oxygen pressure of 100 psi, with chloride as a catalyst, and reportedly achieve copper extractions of about 95% with a light regrinding of flotation concentrate to a p95 of 45 ìðé [2]. In spite of this satisfactory extraction result, the leach residues contain significant amounts of conglomerates which contain a small amount of unreacted concentrate [2], The conglomerations are formed because the elemental sulfur generated is liquid and sticky (melting point of sulfur being 119°C), and has a tendency to wet the sulfide mineral surface, a fact which inhibits the oxidation of the minerals. The overall process chemistry of the CESL process may be summarized as follows [3]:"

Jan 1, 2012

By D. E. Moore

The strength of a natural serpentinite gouge was measured at 400°C and an effective pressure of 100 MPa. The strength of the gouge decreased with increasing pore pressure to 50 MPa and then was nearly constant between 50 and 125 MPa. The samples at 50-125 MPa pore pressure slid stably, whereas those at 3-25 MPa pore pressure showed stick-slip behavior. Lengthening the pre-heating time to 72,000 s of samples at 100 MPa pore pressure led to increases in both the strength and the likelihood of sliding unstably. With still longer pre-heating times, the strengths decreased again and sliding once more became stable. The strength of the gouge at 3 MPa pore pressure was unaffected by changes in pre-heating time. A possible explanation for the results is that excess pore pressures are being generated in the gouge, causing the true effective pressure to be lower than the apparent value.

Jan 1, 1984

By Gustavo A. Munoz

Activated carbons owe their adsorption capacities to their extensively developed pore network structure. As a result, these adsorbents generally exhibit high specific surface areas. Currently, granular activated carbons produced from coconut shells are traditionally used for gold recovery by adsorption from cyanide leaching solutions. Magnetic activated carbons (MACs) for gold recovery from cyanide solutions produced from sources other than coconut shells have been developed at the University of Utah by mixing a magnetic precursor with a carbon source, and treating the mixture under controlled conditions of temperature and gas phase composition. The pore size distribution of the activated carbons is dependent on the degree of activation, among other factors. The significance of the MAC pore size distribution on gold adsorption kinetics and gold adsorption capacity is presented.

Jan 1, 2003

By Agus Sasmito, Akash Adhikari, Srivatsan Jayaraman Sridharan, Purushotham Tukkaraja

Previous studies on blast fumes(CO + NO2) clearance and workplace re-entry time have overlooked the effects of toxic gases entrapped in the muckpile. The currently available models forcalculatingthe mine re-entry times assume that all post-blast fumes are emitted upon detonation. However,recentstudies reportedthat as much as 60% to 70% of the fumes or gases produced during an underground development blasting couldremain entrapped in the adjacent rock mass or in the muckpile. Entrapped fumes are slowly released,and when disturbed, high concentrations are released, representing a possible risk during the digging and transportation of the muckpile. This study uses CFD, SC-Flow software to understandthe behaviorof the entrapped fumes and theireffect on mine re-entry time.

Feb 1, 2020

By K. Zhang

Real option value (ROV) method is considered to be more practical and advanced compared to net present value (NPV) method in evaluating a mining project, in particularly when there is substantial uncertainty in the commodity market as well as possible operational flexibility embedded in the project. Usually, it may take months or even years for the commodity product to be available in the market after the mining activation decision is made. The impacts of postponing the delivery of commodity product on the mine?s ROV and NPV are assessed based on the proposed real option method. Postponing the delivery of the products leads to declined NPV and ROV compared to the non-postponing scenario and extended postpone results in higher lost values in NPV and ROV. For a mine with lower mining cost, by postponing the delivery, the exercising threshold of commodity price is lower because the mine owner anticipates that commodity price may rise during the time of postponing. A mine with higher mining cost requires a higher exercising price threshold to ?lock up? the profit when there is ambiguity of market situation due to the postponing of the delivery.

Feb 23, 2014

By T. Lindstad, J. Kaczorowski

The Boudouard reactivity of single cokes produced from selected bituminous coals and commercial cokes has been investigated in a thermo gravimetric furnace. The effect of potassium as a catalyst for this reaction was studied, as it is known to accumulate in ferromanganese furnaces. A gaseous impregnation technique using K2CO3 as the potassium source was applied to impregnate the coke samples. The reactivity experiments were designed to simulate conditions occurring in an industrial furnace, as used for production of Mn-alloys. The coke particle size varied from 3.35 to 6.63 mm, while the temperature was maintained between 800- 1100oC with a gas composition from 50 to 75% CO2 in a CO/CO2 mixture. To determine the catalytic effect of potassium, the concentration varied from a fraction of a percent up to 15%wt. The results show that single chars vary significantly in reactivity, depending on the properties of the parent coal, while commercial cokes exhibit similar reaction rates. Temperature and partial pressure of CO2 have the strongest influence on the reactivity, while the influence of gas flow rate and coke particle size were found to be negligible. The catalytic studies revealed that the relative reactivity of non-impregnated samples are preserved after the impregnation, so the least reactive coke is still the least reactive after the impregnation for the whole range of potassium loads. Also, it has been confirmed that the Boudouard reactivity reaches a plateau at potassium concentration of 4%wt.

Jan 1, 2007

This paper examines the hypothesis that the fragment size distribution of blasted rock contains information about the changes in fragment sizes with distance from the borehole, and that this information can be interpreted and used to predict the effect of powder factor on fragmentation. A set of simple relationships between the fragment size distribution curve and the dependence of fragmentation on powder factor is proposed. The equations derived are compared with published data on fragmentation in small scale blasting. Two data sets were analyzed, and the results confirm the hypothesis.

Jan 1, 1997

By A A. Struthers, A D. Farmer

Power ultrasound may be applied to enhancing the processing of minerals. The enhanced performance is achieved through the very localised high-energy release at the mineral surface from the collapse of cavitation bubbles produced by power ultrasound. This gives rise to two effects: initially, the rapid cleaning of mineral surfaces û of oxidation products and coatings of fine adhering gangue minerals û and the attenuation of the boundary layer at the mineral surface during leaching, which allows fresh leachant to contact the surface more readily. Work carried out at CSIRO in conjunction with Tiwest Joint Venture has demonstrated that it is feasible to apply ultrasound to the leaching process in order to enhance the removal of contaminating minerals. When applied to the production of synthetic rutile from reduced ilmenite produced by the Becher process, the use of ultrasound proved beneficial to both the aeration and the final acid leach process. The effect of ultrasound was less marked in the case of the aeration process, once the method of introducing and dispersing the air was optimised. In the subsequent acid leaching step of the Becher process it was found that the application of power ultrasound could reduce leaching time to about one quarter of the time required when only agitation was employed. Projected capital and operating costs, based on currently available commercial equipment, are also presented, and indicate that the use of ultrasound is commercially as well as technically feasible.

Jan 1, 2001

By Raymond H. Green, Mitchell W. Green

The authors examined the application of precise millisecond delay electric blasting at a well-known Vermont quarry. The paper explains how the use of a new high-accuracy electric delay detonator has improved fragmentation, raised productivity 10%, simplified blast design, and increased the ability to predict results from blasting.

Jan 1, 1986