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hs code for iron ore beneficiation

beneficiation of iron ore

beneficiation of iron ore

Beneficiation of Iron Ore and the treatment of magnetic iron taconites, stage grinding and wet magnetic separation is standard practice. This also applies to iron ores of the non-magnetic type which after a reducing roast are amenable to magnetic separation. All such plants are large tonnage operations treating up to 50,000 tons per day and ultimately requiring grinding as fine as minus 500-mesh for liberation of the iron minerals from the siliceous gangue.

Magnetic separation methods are very efficient in making high recovery of the iron minerals, but production of iron concentrates with less than 8 to 10% silica in the magnetic cleaning stages becomes inefficient. It is here that flotation has proven most efficient. Wet magnetic finishers producing 63 to 64% Fe concentrates at 50-55% solids can go directly to the flotation section for silica removal down to 4 to 6% or even less. Low water requirements and positive silica removal with low iron losses makes flotation particularly attractive. Multistage cleaning steps generally are not necessary. Often roughing off the silica froth without further cleaning is adequate.

The iron ore beneficiation flowsheet presented is typical of the large tonnage magnetic taconite operations. Multi-parallel circuits are necessary, but for purposes of illustration and description a single circuit is shown and described.

The primary rod mill discharge at about minus 10- mesh is treated over wet magnetic cobbers where, on average magnetic taconite ore, about 1/3of the total tonnage is rejected as a non-magnetic tailing requiring no further treatment. The magnetic product removed by the cobbers may go direct to the ball mill or alternately may be pumped through a cyclone classifier. Cyclone underflows usually all plus 100 or 150 mesh, goes to the ball mill for further grinding. The mill discharge passes through a wet magnetic separator for further upgrading and also rejection of additional non-magnetic tailing. The ball mill and magnetic cleaner and cyclone all in closed circuit produce an iron enriched magnetic product 85 to 90% minus 325 mesh which is usually the case on finely disseminated taconites.

The finely ground enriched product from the initial stages of grinding and magnetic separation passes to a hydroclassifier to eliminate the large volume of water in the overflow. Some finely divided silica slime is also eliminated in this circuit. The hydroclassifier underflow is generally subjected to at least 3 stages of magnetic separation for further upgrading and production of additional final non-magnetic tailing. Magnetic concentrate at this point will usually contain 63 to 64% iron with 8 to 10% silica. Further silica removal at this point by magnetic separation becomes rather inefficient due to low magnetic separator capacity and their inability to reject middling particles.

The iron concentrate as it comes off the magnetic finishers is well flocculated due to magnetic action and usually contains 50-55% solids. This is ideal dilution for conditioning ahead of flotation. For best results it is necessary to pass the pulp through a demagnetizing coil to disperse the magnetic floes and thus render the pulp more amenable to flotation.

Feed to flotation for silica removal is diluted with fresh clean water to 35 to 40% solids. Being able to effectively float the silica and iron silicates at this relatively high solid content makes flotation particularly attractive.

For this separation Sub-A Flotation Machines of the open or free-flow type for rougher flotation are particularly desirable. Intense aeration of the deflocculated and dispersed pulp is necessary for removal of the finely divided silica and iron silicates in the froth product. A 6-cell No. 24 Free-FlowFlotation Machine will effectively treat 35 to 40 LTPH of iron concentrates down to the desired limit, usually 4 to 6% SiO2. Loss of iron in the froth is low. The rough froth may be cleaned and reflotated or reground and reprocessed if necessary.

A cationic reagent is usually all that is necessary to effectively activate and float the silica from the iron. Since no prior reagents have come in contact with thethoroughly washed and relatively slime free magnetic iron concentrates, the cationic reagent is fast acting and in somecases no prior conditioning ahead of the flotation cells is necessary.

A frother such as Methyl Isobutyl Carbinol or Heptinol is usually necessary to give a good froth condition in the flotation circuit. In some cases a dispersant such as Corn Products gum (sometimes causticized) is also helpful in depressing the iron. Typical requirements may be as follows:

One operation is presently using Aerosurf MG-98 Amine at the rate of .06 lbs/ton and 0.05 lbs/ton of MIBC (methyl isobutyl carbinol). Total reagent cost in this case is approximately 5 cents per ton of flotation product.

The high grade iron product, low in silica, discharging from the flotation circuit is remagnetized, thickened and filtered in the conventional manner with a disc filter down to 8 to 10% moisture prior to treatment in the pelletizing plant. Both the thickener and filter must be heavy duty units. Generally, in the large tonnage concentrators the thickener underflow at 70 to 72% solids is stored in large Turbine Type Agitators. Tanks up to 50 ft. in diameter x 40 ft. deep with 12 ft. diameter propellers are used to keep the pulp uniform. Such large units require on the order of 100 to 125 HP for thorough mixing the high solids ahead of filtration.

In addition to effective removal of silica with low water requirements flotation is a low cost separation, power-wise and also reagent wise. Maintenance is low since the finely divided magnetic taconite concentrate has proven to be rather non-abrasive. Even after a years operation very little wear is noticed on propellers and impellers.

A further advantage offered by flotation is the possibility of initially grinding coarser and producing a middling in the flotation section for retreatment. In place of initially grinding 85 to 90% minus 325, the grind if coarsened to 80-85% minus 325-mesh will result in greater initial tonnage treated per mill section. Considerable advantage is to be gained by this approach.

Free-Flow Sub-A Flotation is a solution to the effective removal of silica from magnetic taconite concentrates. Present plants are using this method to advantage and future installations will resort more and more to production of low silica iron concentrate for conversion into pellets.

limonite siderite iron ore beneficiation

limonite siderite iron ore beneficiation

A laboratory mineral-dressing investigation was conducted by the Federal Bureau of Mines on four limonitic and four sideritic iron ores from the North Basin of the east Texas iron-ore district. The samples, composited from drill cores, were considered representative of the iron-ore reserves of the area. The objectives of this research were twofold: (1) To devise a mineral-dressing method whereby the yield from currently mined east Texas iron ores might be increased and the grade improved, and (2) to extend such treatment to include the lower grade ferruginous materials that are not amenable to beneficiation by simple washing and, therefore, are not being exploited. Of the mineral-dressing methods used in this investigation, magnetic separation of roasted ore was shown to be the most effective. Results show that, by this method, a laboratory recovery of 82 percent of the iron is attainable at a grade surpassing that obtained by current plant practice and that both limonite and siderite are amenable to concentration by the process.

The existence of large deposits of iron ore in eastern Texas has been recognized for over 100 years. These ores were first exploited during the Civil War and were mined intermittently until about 1911. From that time until 1944 when the Defense Plant Corporation financed the erection of three blast furnaces to use these east Texas ores, production was almost at a standstill.

The Sheffield Steel Co. concentrator uses a comparatively high-grade feed, containing 35 percent or more of Fe, and produces concentrates averaging more than 44 percent Fe by a comparatively simple washing operation.

The Lone Star Steel Co. concentrator feed averages about 23 percent Fe. This feed is one of the lowest grade iron ores currently being used in this country. The process, in brief, involves stage crushing, with intervening scrubbing and sizing to remove fine gangue and recover coarse iron minerals.

The low recovery obtained by the commercial concentrators, together with the large reserves of low-grade ore in the east Texas field, prompted the Bureau of Mines to undertake research to develop methods for increasing the recovery of iron from the ores of plant-feed grade and for extending the methods to those ores not amenable to existing plant practice.

In the North Basin area of the east Texas iron-ore district, the ore occurs principally as horizontal ledges and lenses in weathered greensand. The oxide zone is 45 feet thick or more, while the carbonate zone is as much as 65 feet. Recent figures released by the Bureau of Mines show a reserve of 160 million long dry tons of ore in the North Basin that could be washed to a grade of 40 percent Fe.

To obtain the large representative ore samples required for this investigation, the Bureau of Mines drilled 56 holes 7 inches in diameter on 4 properties in the North Basin. These properties are held by the Lone Star Steel Co. through either warranty or iron-ore deeds and consist of the Connors, Pouns, and Lattimer properties in eastern Morris County and the Pynson property in western Cass County. The total footage drilled amounted to 2,145 feet, of which 840 feet was in brown iron ore, 806 feet in carbonate ore, and 499 feet in waste. Selected drill cuttings were combined for metallurgical samples.

The samples consisted of brown iron ore (limonite) and carbonate ore (siderite). The limonite was composed of both amorphous and crystalline oxides; the siderite was dense and crystalline. Principal impurities were siliceous, free silica as quartz sand, siliceous clay, and residual grains of the hydrous silicate, glauconite. Partial chemical analyses of the individual ores are given in table 1.

Previous work by the Bureau of Mines showed that limonitic ores from the North Basin could be upgraded to an acceptable, but low-grade, concentrate by a simple washing-sizing treatment. Current plant practice in the east Texas field results in a grade concentrate similar to that obtained by washing and sizing the limonitic and sideritic ores investigated. For this study, all samples were crushed to minus 1-inch and blunged at 50 percent solids for 1 hour in a 12-inch-diameter mill equipped with four equispaced lifters. The iron minerals in the scrubbed ores were separated by screening on 10-mesh and 48-mesh sieves; the minus 48-mesh fraction was further classified in a hydrocyclone.

Comparative test runs of blunging in water only and blunging in water containing 1 pound per ton each of sodium silicate and sodium hydroxide showed almost identical recoveries and grade of concentrate. Therefore, the results of blunging with water containing sodium silicate and sodium hydroxide are not tabulated in this report.

With the laboratory washing-sizing process, limonite ores from the Connors, Pouns, and Pynson properties yielded concentrates averaging 41.0 percent Fe and 24.7 percent acid insoluble material and representing a recovery as high as 46.0 percent of the total iron (tables 2, 3, and 4). The overall concentrate grade and iron recovery approached commercial plant results in the east Texas field. Experiments on the Lattimer limonite (table 5) failed to produce the 40 percent iron concentrate that was considered the minimum acceptable grade. The siderite ores also failed to yield a 40 percent iron concentrate (tables 2, 3, 4, and 5).

Magnetic separation is a simple, yet often effective, method of ore concentration usually considered in investigations concerned with the separation and recovery of iron minerals. Iron-hearing minerals that can be beneficiated by this means are (1) naturally occurring magnetite and (2) the paramagnetic products of the roasting of iron-bearing minerals.

Iron carbonate changes to a magnetic oxide by thermal decomposition. Carbon dioxide begins to evolve endothermically at about 300 C. to form FeO; an exothermic reaction follows, if oxygen is available for reaction with ferrous oxide. When iron carbonate is roasted in an inert atmosphere, some nonmagnetic ferrous oxide results; when it is roasted with full access to air, the nonmagnetic ferric oxide is formed. Best results are obtained under the weakly oxidizing conditions that exist when the furnace vents are open to the air but with no forced draft.

The ores investigated included limonite and siderite. Roasting research covered the individual ore types as well as composites of the two. Although the individual samples were considered as either limonite or siderite, they were in reality contaminated, one with the other, with the siderite containing a large amount of ferric iron and the limonite a lesser amount of ferrous iron (table 1, p. 3).

As preliminary work revealed that both the limonite and siderite could be roasted effectively at 1-inch size, all roasting tests were made on ore sized to minus 1-inch, unless otherwise specified. Except for a brief investigation of flash roasting, all roasts were made in an externally fired drum roaster, with provision for close control of both roaster temperature and atmosphere. This roaster is shown in figure 1.

The optimum conditions of roasting the limonite ores, as determined by controlled time, temperature, and furnace atmosphere variables, were found to be a 30-minute roast at 600 C. in carbon monoxide. These conditions were established by varying the temperature of the roast from 400 to 700 C. at 50 intervals; time of roast from 15 to 40 minutes; and atmospheres from carbon monoxide to hydrogen, propane, and mixtures of propane and air.

The optimum roasting conditions for the siderite ore were a 15-minute roast at 500 C. in the gases resulting from the decomposition of the ore. Temperatures of roast studied varied from 400 to 600 C. and roasting time from 5 to 30 minutes; furnace atmospheres used were atmospheric air, helium, and gases resulting from the decomposition of the ore.

Mixed limonite-siderite ores were subjected to an oxidizing roast before the reduction. Controlled variables of reduction were the same as for the limonite ore. Optimum conditions determined were a 20-minute roast at 550 C. in carbon monoxide.

Magnetic separations were made with a Wetherill high-intensity crossbelt separator, used as a rougher, and with a Davis-tube magnetic separator, used as a cleaner or finisher for the Wetherill magnetic concentrate. Other separators used were a Jeffrey wet drum, a high-intensity induced roll, and an a.-c., traveling-field, experimental unit made in the local laboratories.

The limonite ore of this deposit was of low grade; the metallurgical sample contained 23.3 percent Fe and 50.2 percent acid insoluble matter. Most of the iron was present as limonite, with only 3 percent of the total iron as the carbonate.

In a typical roasting test on this ore, magnetic ferroso-ferric oxide was formed by roasting for 30 minutes at 600 C. in an atmosphere of carbon monoxide. Magnetic separation in a Davis tube recovered 84.1 percent of the total iron in a concentrate containing 49.4 percent Fe and 17.9 percent acid insoluble material.

Siderite ore from the Connors Brothers deposit was higher in iron content than the limonite ore. It contained 30.6 percent iron and 26.4 percent acid insoluble material. Of this total iron, however, only 71 percent was present as the carbonate.

When the ore was roasted for 15 minutes at 500 C. in the atmosphere resulting from the thermal decomposition of the carbonate (mostly CO2), only the siderite was converted to the magnetic ferroso-ferric oxide owing to insufficient reductant present in the furnace atmosphere to reduce a large portion of the limonite. Separation of the ore roasted under these conditions recovered 71.9 percent of the total iron in a concentrate containing 53.9 percent Fe and 13.3 percent acid insoluble material.

Roasting of a composite of equal weights of two ore types for 20 minutes at 550 C. in an atmosphere of carbon monoxide, followed by magnetic separation in a Davis tube, recovered 79.0 percent of the total iron in a concentrate containing 49.9 percent Fe and 17.2 percent acid insoluble matter.

Limonite ore from the Pouns deposit with an iron content of 30.7 percent and 35.4 percent acid insoluble was the highest grade ore used in this investigation. Of the total iron in this ore, 8.0 percent was in the carbonate form.

Roasting this ore for 30 minutes at 600 C. in an atmosphere of carbon monoxide, followed by magnetic separation at minus 100-mesh, resulted in the recovery of 81.9 percent of the total iron in a magnetic concentrate containing 49.9 percent Fe and 18.3 percent acid insoluble.

This ore was roasted under the previously determined optimum conditions of 500 C. for 15 minutes in an atmosphere composed of the gases produced by the decomposition of the ore. Magnetic separation recovered 52.8 percent of the total iron in a magnetic concentrate containing 50.8 percent Fe and 13.5 percent acid insoluble. The low recovery is due, in part, to the small percentage of total iron present in the ferrous state for the transformation to the paramagnetic form under roasting conditions employed and to the high content of iron-bearing clay in this ore.

Roasting of a composite of equal weights of limonite and siderite ores at 500 C. for 20 minutes in an atmosphere of carbon monoxide, followed by magnetic separation in a Davis tube, resulted in the recovery of 64.8 percent of the total iron in a magnetic concentrate containing 51.9 percent Fe and 15.8 percent acid insoluble. Table 7 gives the results of these tests.

The limonite ore from the Pynson property was also of very low grade, containing 21.3 percent Fe and 51.4 percent acid insoluble. It consisted almost entirely of ferric iron, with only 3 percent of the total being in the ferrous state.

The ferroso-ferric oxide formed by roasting at 600 C. for 30 minutes in an atmosphere of carbon monoxide was recovered by magnetic concentration in a Davis tube. This concentrate, containing 49.4 percent Fe and 17.5 percent acid insoluble, represented a recovery of 78.3 percent of the total iron in the crude ore.

This carbonate ore was of even lower grade than the limonitic ore, with only 19.7 percent iron content and 45.3 percent acid insoluble. Of the total iron present, 64.5 percent was in the ferrous state.

Roasting for 15 minutes at 500 C. in an atmosphere consisting mainly of the gases resulting from thermal decomposition of the ore (carbon dioxide and water vapor), followed by magnetic separation, resulted in the recovery of 58.9 percent of the total iron in a concentrate containing 49.9 percent Fe and 12.7 percent acid insoluble.

A sample containing equal weights of the two ore types was roasted for 20 minutes at 550 C. in an atmosphere of carbon monoxide and then magnetically separated. This treatment produced a magnetic concentrate containing 52.6 percent Fe and 15.2 percent acid insoluble, representing a recovery of 65.7 percent of the total iron. Results are tabulated in table 8.

The limonite ore was the lowest in grade of all the limonitic ores investigated, with an iron content of 21.0 percent and an acid insoluble content of 53.5 percent. Like the other limonitic ores, it contained little ferrous iron,with only 3 percent of the total being in this reduced state.

Reduction roasting at 600 C. for 30 minutes in an atmosphere of carbon monoxide, followed by magnetic separation in the Davis tube, recovered 70.5 percent of the total iron in a magnetic concentrate containing 48.4 percent Fe and 19.4 percent acid insoluble.

When roasted for 15 minutes at 500 C. in an atmosphere of decomposition gases and separated in a Davis tube, this ore responded, as other siderites in previous tests, with a low recovery of iron. The magnetic concentrates contained 49.2 percent Fe and 15.4 percent acid insoluble and represented 60.2 percent of the total iron.

A composite of equal weights of the two Lattimer ores, when roasted at 550 C. for 20 minutes in an atmosphere of carbon monoxide, followed by magnetic separation, resulted in the recovery of 64.1 percent of the total iron in a magnetic concentrate containing 49.1 percent Fe and 17.3 percent acid insoluble. Summation of results is given in table 9.

The investigation of roasting and magnetic separation, as applied to the several individual ores and to composites of both ore types from each property, considered only the variables of roasting time, roasting temperature, and furnace atmosphere. Further research to study other techniques, such as oxidizing the ore before reduction, wet versus dry magnetic separations, and the relative magnetic susceptibilities of magnetite and gamma-hematite, was conducted on a composite of equal weights of all eight of the ores.

The first approach to the problem of mixed-ore types, with their varied requirements for magnetic roasting, was by roasting in an atmosphere of ore-decomposition products. According to Mellor, it is probable that ferrous carbonate first splits into ferrous oxide and carbon dioxide and that these react on one another to give ferric oxide and carbon monoxide. The intent of this roasting was to use the carbon monoxide released from the thermal decomposition of siderite to reduce the limonitic iron oxides. This technique was not successful, as the amount of magnetic iron oxide produced was barely sufficient to account for the iron originally contained in the siderite. Analysis of the exit gases disclosed no carbon monoxide. The presence of 0.2 to 0.4 percent of free carbon in the roasted ore suggests that carbon monoxide was combining to produce carbon dioxide and free carbon instead of reducing the iron oxides in the ore.

The second approach to this problem was through an oxidizing roast before the reduction roast. When roasted in air, both ferrous carbonate (siderite) and the hydrated iron oxides (limonite) are converted to ferric oxide, which is readily reduced to the magnetic iron oxide, magnetite.

Reduction roasting and magnetic separation of this uniformly oxidized material showed improvement in both grade of concentrate and recovery over that obtained when the different ore types were treated without a prior oxidizing roast.

In a typical test, the ore was first roasted in air at 600 C., then reduced at the same temperature by passing a stream of carbon monoxide through the roaster. The reduced ore was cooled in an inert atmosphere to prevent reoxidation. The temperature of the oxidizing step was shown to have a decided influence on both grade and recovery of the concentrate derived from the reduced ore (tables 10, 11, and 12). Processing at 600 C. resulted in the highest grade concentrate and lowest recovery (50.9 percent Fe and 15.2 percent acid insoluble with a recovery of 75.7 percent), while the ore roasted at 800 C. showed the lowest grade and highest recovery (49.4 percent Fe and 21.9 percent acid insoluble with a recovery of 82.4 percent). The higher recovery results from the recovery of altered glauconite (hydrous silicate of iron and potassium) grains that have become susceptible, in part, to reduction to magnetic iron oxide after a preoxidation treatment at 800 C. The galuconite was, in effect, magnetic but of low iron content. The micrographs of roasted glauconite grains (figs. 2 and 3) show the magnetic iron oxide as white coatings and stringers in a grey matrix of glauconite, thus emphasizing the impracticality of grinding to the degree necessary to liberate this iron oxide.

A series of magnetic oxides of iron may be formed from iron-bearing minerals by roasting under proper conditions of temperature and atmosphere. Magnetite (Fe3O4) and maghemite (Fe2O3) are the end members of what appears to be a continuous series of solid solutions. 14/ Reduction roasting of iron-bearing minerals in hydrogen from 400 to 570 C. results in the formation of a product with, or similar to, the composition of magnetite; above 570 C. ferrous oxide is likely to form. When magnetite is heated in air between 200 and 400 C., it takes in oxygen, the rate and extent being functions of temperature, and the composition approaches that of gamma-hematite (maghemite). This change is accompanied by a substantial increase in volume (7.76 percent), if the final product is maghemite.

In this research, magnetite was oxidized to maghemite to determine which form of the oxide would exhibit the greatest magnetic susceptibility when very finely divided and (2) whether the large expansion accompanying gamma oxidation would tend to loosen the locked magnetite-gangue particles. Results of the study were inconclusive as to magnetic susceptibility. Increased liberation of the gangue particles by the oxidation expansion was not significant, but the oxidation did improve the grindability of the roasted ore.

Effective magnetic separation of iron-bearing minerals does not require that the mineral grain be completely reduced (or oxidized) to a ferromagnetic form. The formation of a relatively thin surface layer of material with high magnetic susceptibility will make the entire grain magnetically separable.

A brief study of this concept of incomplete magnetic roasting was made to determine if the process was technically feasible for the east Texas iron ores. Roasting was accomplished in a vertically mounted electric tube furnace equipped with baffles to control the retention time of the ore and a water seal at the base to permit control of the roasting atmosphere.

At 700 C. in an atmosphere of carbon monoxide, minus 65-mesh ore was reduced in approximately 2 seconds. The reduction appeared to be complete throughout the grains. On minus 6- plus 65-mesh ore, under the same roasting conditions, 7 seconds were required to reduce a surface film. This reduction

made the particles magnetically separable, but further grinding destroyed the film, leaving a core that was not recoverable by magnetic means. Concentrates obtained from this flash-roasted material were of acceptable grade (46 percent Fe and 20 percent acid insoluble), but recovery was limited to 51 percent. One of the chief deterrents to flash roasting is the difficulty of grinding the crude ore to the necessary degree of fineness. On ore fractions, such as washer tailings, that would not require grinding, this roasting may prove valuable. As applied to washer tailings obtained in this research, a magnetic concentrate containing 39.9 percent Fe and 27.6 percent acid insoluble was recoverable. Recovery at this grade was only 16 percent of the total iron, but the feed contained only 15.8 percent Fe, most of which was present as slimes.

application of biotechnology in iron ore beneficiation - sciencedirect

application of biotechnology in iron ore beneficiation - sciencedirect

A biomining approach to process low-grade iron ores has the potential to turn closed mines or uneconomic mineral deposits into economic resources. Microorganisms and their metabolites have been commercially applied in the leaching of metals from medium- and low-grade sulfide minerals for many years. Efforts are now being directed to the application of biomining to oxide ore systems as high-grade ore becomes scarce. This chapter discusses the potential exploitation of microorganisms and their metabolites for the bioleaching of phosphorus from iron ore and as bioreagents for the selective flotation and flocculation of iron ore minerals.

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