US3782539A - Beneficiation of phosphate ores - Google Patents

Beneficiation of phosphate ores Download PDF

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US3782539A
US3782539A US00194456A US3782539DA US3782539A US 3782539 A US3782539 A US 3782539A US 00194456 A US00194456 A US 00194456A US 3782539D A US3782539D A US 3782539DA US 3782539 A US3782539 A US 3782539A
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/02Froth-flotation processes
    • B03D1/021Froth-flotation processes for treatment of phosphate ores
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03BSEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
    • B03B7/00Combinations of wet processes or apparatus with other processes or apparatus, e.g. for dressing ores or garbage

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  • This invention relates to the beneficiation of certain phosphate ores by which not only is a remarkable amount of the total phosphate in the ore recovered in the final product but also the product is at least as rich in phosphate values as obtained by present processes but is frequently richer.
  • the present process eliminates at least two of the essential steps of the prin cipal process now in commercial use, thus reducing costs to a substantial extent as will be explained more fully hereinafter.
  • virgin phosphate ores differ in numerous respects depending on their geographical location and a process which is suitable for an ore in one area, such as the well known Florida ores, may not be suitable, nor even operable for ores in another area. These differences in the ores are not too well understood and may be attributed to physical as well as chemical differences in the gangue materials since in most phosphate ores the phosphate values, commonly referred to as B.P.L. (Bone phosphate of lime) is in the form of apatite, such as fluorap'atite, having the formula Ca (CaF) (P or other apatites in which the F is replaced by C1 or OH.
  • CaF CaF
  • the non-phosphate portions of the ores usually consist of clay, silica and the like, which may be present in different physical forms which affect the ,beneficiation of the ores. How the physical forms affect the treatment of the ores is not well known since it is usually more economical to test the ores from new deposits by various known processes to determine the one process which gives the best results as to total phosphate recovery and grade of product.
  • a process frequently used in treating Florida ores includes a first flotation step with anionic reagents followed by an acid (H 80 scrubbing treatment to remove the first reagent and a subsequent flotation step with a cationic reagent for final separation of the gangue materials from the phosphate values, such as is described in US. Pat. No. 2,293,640 to Arthur Crago. This process is hereinafter referred to as the Florida Process.
  • a saponified fatty acid concentrate could be cleaned one or more times and that the coarser fraction of the middlings could be screened away from the finer fraction leaving a high grade coarse middling that could report to the final concentrate, and a low grade fine middling that could either report to tailings or back to the head of the circuit.
  • the resultant savings in reagent alone could amount to about $0.20/ton of originally mined crude ore and this would be in addition to the savings in. labor, and in the auxiliary capital equipment required for additional scrubbing, washing, conditioning and flotation.
  • the total reagent savings alone due to the elimination of the acid step would amount to about $1M; million per year and the savings due to the elimination of the cationic reagent would be about 513% million a year.
  • FIG. 1 illustrates a flow diagram of one method of carrying out the process
  • FIG. 2 illustrates a second form of a flow diagram for carrying out the present invention.
  • FIG. 1 illustrates the process in which the phosphate ore as mined is first crushed to about 20 mesh and is then treated with water in a first scrubber l for about 2 minutes and then is subject to a screening 2 at about 20 mesh (Standard Tyler screen sizes). Any oversized material at about +20 mesh may be reground in a grinder 2a and returned to the scrubber while the undersize material at 20 mesh is fed to a deslimer 3.
  • the desliming step may be carried out in cyclone separators or by very fine screens so as to effect a separation at about 500 mesh.
  • the undersized material at about 500 mesh is slime and is discarded to waste.
  • the oversized ore material having a size of +500 mesh is preferably passed to a second scrubber 4 and scrubbed for about 2 minutes and then passed to a second deslimer 5, the slime overflow from which may be recycled to the first deslimer.
  • the second scrubber 4 and second deslimer 5 may be eliminated so that the +500 mesh material from the first deslimer 3 may be passed directly to a sizing device.
  • the sand material from deslimer 5 at about +500 mesh is diluted with water and the slurry passed through the sizing device or screen 6 to make a separation at about 100 mesh.
  • the sizing device or screen 6 separates the deslimed ore into two fractions one comprising a coarse fraction of about by +100 mesh and the other a finer fraction of about -l00 by +500 mesh.
  • the coarser fraction is passed to a classifier 7 in which some of the water and possibly a small amount of fine particles is removed leaving an underflow sand fraction comprising about 75 percent solids.
  • This fraction is passed to a drum conditioner 8 to which is added an anionic flotation reagent and certain other reagents to be described further hereinafter.
  • the ore material is thoroughly conditioned with the anionic flotation reagents it is passed to the rougher flotation cells 9.
  • the flotation tailings, or underflow from the cells 9 are discarded along with other tailings as described further below.
  • the flotation concentrate, without any further addition of reagents is passed to the cleaner flotation cells 10, the flotation tails from which are discarded and the flotation concentrate from which forms a portion of the final concentrate.
  • the finer fraction from screen 6 having a size of from l00 by +500 mesh is passed to a thickener 11.
  • a thickener may be added the overflow from classifier 7, if desired, and the overflow from the thickener 11 is removed for reuse in the process wherever dilution is called for as for example to scrubber l, deslimer S or sizing device 6.
  • the ore pulp coming from the underflow of the thickener 11 comprises about 75 percent solids. This pulp is passed to drum conditioner 12 to which anionic flotation reagents are added as will be described further hereinafter.
  • the flotation concentrate without any further addition of reagents is passed to cleaner flotation cells 14..
  • the cleaner flotation tailings from these cells are preferably recycled to the rougher flotation cells 13 for retreatment.
  • the flotation concentrate from the cleaner flotation cells 14 without the addition of further reagents may be passed to recleaner flotation cells 15 for further upgrading and concentration of phosphate values in the ore.
  • the flotation tails from the recleaner cells 15 are preferably recycled to the cleaner flotation cells 14 and the flotation concentrate is combined with the final concentrate from the cleaner flotation cells 10 obtained from the treatment of the coarse ore fraction.
  • the same procedure is followed through elements 1 6 and the finer fraction, i.e. l00 by +500 mesh, is treated in the same fashion through elements 11 15.
  • the coarser fraction after passing through elements 7 9 is subjected to a different and more refined treatment.
  • the tailings from the rougher flotation cells 9 are passed through a fine screen 16 which may be a DSM type screen provided with a knocking device to facilitate screening. If desirable the screen may be from about 28 mesh to about 65 mesh, and the oversized material is passed through a grinder 17 such as a wet hammer mill or rod mill and returned to the thickener 11 for the finer fraction, while the undersized material is passed to the final tailings.
  • the concentrate from the rougher flotation cells 9 are passed, as before, to cleaner flotation cells 10.
  • the tails therefrom are passed through a screen 18 of the types mentioned above for screen 16.
  • the undersized fraction therefrom is recycled to the rougher flotation cells 9 or altematively passed with the material from grinder 17 to thickener 11, or, if desired, passed directly to final tailings.
  • the oversized material is passed to the final concentrate.
  • this step may be car ried out by the use of a fixed, flat or curved screening surface, mounted on an incline, and of the Dutch State mines type of screen.
  • a knocking device To the rear side of the frame of the screen there may be attached a knocking device to prevent the screen from blinding.
  • total flot. feed 78.21 27.31 86.51 18. total flot. cone. 25.10 75.54 76.75 19. total rougher tails 46.98 3.43 6.55 20. total cleaner-recleaner 6.13 12.82 3.21 tails 21. total slimes 21.79 15.29 13.49
  • the'desliming steps are performed at about 500 mesh instead of the conventional 150-200 mesh and this has the immediate effect of reducing phosphate losses from about percent to about 15 20 percent.
  • Tne anionic reagents employed in the foregoing processes are comprised of fatty acid tall oil and fuel oil. While the ratio of fatty acid tall oil and fuel oil may vary within rather wide limits, the ratio is generally maintained at from about 1.5 to l to about 2.5 to 1. In Table 1 relating to FIG. 1, 4.9 lbs. of the fatty acid tall oil and 2.2 lbs of fuel oil were used per dry short ton of crude ore while in Table 11 relating to FIG. 2 the anionic reagents comprises 5.5 lbs. of fatty acid tall oil and 3.2 lbs. of fuel oil per dry short ton of crude ore.
  • the Florida ores when subject to the anionic flotation-acid scrubbing-cationic flotation procedure commonly used as mentioned above give a final recovery of phosphate values from about 50 percent 60 percent based on the crude ore, whereas according to the present process the final recovery of phosphate values is in the range of 65 percent 80 percent.
  • a process for the beneficiation of phosphate ore comprising scrubbing the ores at least once, desliming the scrubbed ore at about 500 mesh after each of said at least one scrubbing steps, separating the deslimed ore at about 100 mesh to produce a coarse fraction and a fine fraction, passing the coarse fraction through a classifier to produce an overflow and a coarse slurry containing about percent solids, conditioning the coarse slurry with anionic flotation reagents, subjecting said conditioned coarse slurry to treatment in at least one rougher flotation machine to produce rougher tailings and a rougher concentrate, treating the concentrate in at least one cleaner flotation machine to produce tailings and a final concentrate, passing the fine fraction through a thickener to produce a time slurry containing about 75 percent solids, conditioning the fine slurry with anionic flotation reagents, subjecting the conditioned fine slurry to treatment in at least one rougher flotation machine to produce tailings and a concentrate, treating the concentrate in at least one

Abstract

A process for beneficiating phosphate ores in which the ore is scrubbed and deslimed prior to separation into a coarse fraction and a fine fraction, each of which is subjected to a plurality of anionic flotation steps and screening steps to obtain high recovery and high grade phosphate product whereby the acid cleaning and cationic flotation steps previously used are eliminated.

Description

United States Patent [191 Painter 7 BENEFICIATION OF PHOSPHATE ORES [75] Inventor: William Howard Painter, Hibbing,
Minn. v [73] Assignee: PM Holding Co., Cleveland, Ohio [22] Filed: Nov. 1, 1971 [21] App]. No.: 194,456
[52] US. Cl 209/2, 209/17, 209/166 [51] Int. Cl. B03b 9/00 [58] Field of Search 209/12, 161, 167, 209/2, 17; 241/20, 24
[56] References Cited UNITED STATES PATENTS 1,912,434 6/1933 Crago 209/166 2,156,245 4/1939 Mead 209/166 3,086,654 4/1903 Hollingsworth 209/166 3,032,197 5/1902 Northcott 209/166 3,098,817 7/1963 Baarson 209/166 Jan. 1, 1974 3,137,650 6/1964 Smith 209/12 3,282,418 11/1966 Abernethy. 209/12 3,349,903 10/1967 Olsen 209/166 X 3,388,793 6/1968 Dibble 209/166 X 3,40,813 9/1968 Clitheroe 209/166 X 3,483,974 12/1969 Pearsall 209/382 X 2,914,173 11/1959 LeBaron 209/166 Primary Examiner-Robert Halper Att0rney.lohn P. Maxey and Richard J. Minnich ABSTRACT A process for beneficiating phosphate ores in which the ore is scrubbed anddeslimed prior to separation into a coarse fraction and a fine fraction, each of which is subjected to a plurality of anionic flotation steps and screening steps to obtain. high recovery and high grade phosphate product whereby the acid c1eaning and cationic flotation steps previously used are eliminated.
8 Claims, 2 Drawing Figures 1 PHOSPHATE one *2 2 JGRINDER I a t (OVERSIZE) StZING DEVlCE OOM) [SCREEN (ZOMlk SLIMES (-500 MESH) TO WASTE DVERFLOW TO REUSE ROUGHER FLOTATION CLEA J ER FL-QTATION (OVERFLOW) CLEANE R FLDTATIO N RECLEANER FLD'I'ATION FINAL CONCENTRATES FINAL TAILINGS PATENTEDJAH 1 I974 SHEET 1 BF 2 PHOSPHATE ORE SCRUBBER H2O 20L G \N SCREEN (20m (OVE SIZE) w SLiMES DESLIMER (-500 MESH) To WASTE SCRUBBER F4 5 DESLIMER I H OVERFLOW 6 To REUSE' SIZING DEVICE (-20 e nooMs (IOOM) 8 DRUM (ANIONICI REAGENTS) DRUM Conan-mourn CONDITIONER i2. 'gTA|Ls ROUGHER 'ROUYGHE'R FLOTATION' F'LOTATION (TA|LS CLEANER, CLEANER FLOTATION 14 F'LOTAT\ON 'RECLEANER ,5 FLOTATION f\ I L r FINAL FINAL CONCENTRATES TAILINGS Flgj 1 BENEFICIATION OF PHOSPHATE ORES This invention relates to the beneficiation of certain phosphate ores by which not only is a remarkable amount of the total phosphate in the ore recovered in the final product but also the product is at least as rich in phosphate values as obtained by present processes but is frequently richer. In addition, the present process eliminates at least two of the essential steps of the prin cipal process now in commercial use, thus reducing costs to a substantial extent as will be explained more fully hereinafter. i
As is known, virgin phosphate ores differ in numerous respects depending on their geographical location and a process which is suitable for an ore in one area, such as the well known Florida ores, may not be suitable, nor even operable for ores in another area. These differences in the ores are not too well understood and may be attributed to physical as well as chemical differences in the gangue materials since in most phosphate ores the phosphate values, commonly referred to as B.P.L. (Bone phosphate of lime) is in the form of apatite, such as fluorap'atite, having the formula Ca (CaF) (P or other apatites in which the F is replaced by C1 or OH. The non-phosphate portions of the ores usually consist of clay, silica and the like, which may be present in different physical forms which affect the ,beneficiation of the ores. How the physical forms affect the treatment of the ores is not well known since it is usually more economical to test the ores from new deposits by various known processes to determine the one process which gives the best results as to total phosphate recovery and grade of product.
A process frequently used in treating Florida ores includes a first flotation step with anionic reagents followed by an acid (H 80 scrubbing treatment to remove the first reagent and a subsequent flotation step with a cationic reagent for final separation of the gangue materials from the phosphate values, such as is described in US. Pat. No. 2,293,640 to Arthur Crago. This process is hereinafter referred to as the Florida Process.
A general representative metallurgical balance of the Florida Process is shown below:
it: B.P.L.Recovery Product Weight B.P.L. Based Based on on Ore Flot Feed Crude Ore (Matrix) 100.0 20.0 100.0 Slime 30.0 20.0 30.0 FloLConc. 16.2 69.0 56.0 80.0 Slimes Fiot.Tails 83.8 10.5 44.0 20.0
In addition to the substantial phosphate ore deposits in Florida, there are substantial deposits in Tennessee, North Carolina and elsewhere, which may be beneficiated by similar processes. Another known deposit of importance is to be found in Angola, West Africa and more precisely inthe District of Cabinda. Major deposits are located 35 to 30 kilometers from the Atlantic coast port city of Ladana, in the Massabi Formation and consists of interbedded sand, clay, silt, foraminifera limestone, granular calcite and/or dolomite, with phosphate occurring as pellets or nodules, with organic remains. The phosphate is believed to be in the form of fluorapatite.
The Florida process was first used on the ores found in Angola and gave very poor results in that not only was much of the phosphate values lost to the slimes, but of even greater significance, the cationic flotation step which normally floats the remaining silica did not do so on this ore. Various modifications and variations of the main process were attempted with little or no improvement in the results. Finally it was discovered that a process, i.e. the process of the present invention, obtained excellent results and gave, in some respects, results superior to the results obtained on the Florida ores treated by the Florida processes.
The reasons for the failure of the Florida process on the Angola ores are not known wiith certainty, although it is believed that the silica particles may have unusually glassy surfaces which were not coated by the cationic reagents and thus did not flloat. According to the present process as used on Angola ores, it was found that fine silica accompanied larger phosphate particles occurring in the tailing from the cleaner flotation stages as will be described hereinafter and that a separation of one from the other was possible by a screening step.
Although the present process will be described as used on the above mentioned Angola ores, it will be understood that this process may be used advantageously on any ore having characteristics similar to the Angola ores, whereever found and that while the critical characteristics which determine the usefulness of this process are not known and cannot be easily determined analytically, nevertheless the value of the present process in treatment of such ores can be easily determined by comparing results of the Florida process, or other known processes, with the results of the process of the present invention.
In most non-metallic flotation processes, it has been found that if a coarse particle is once floated, as in a rougher flotation operation, it is reluctant to float again, if at all, in a cleaner flotation operation. Therefore, a low grade concentrate must be expected with high recovery or a loss of coarse concentrate in the middlings must be expected if a cleaner operation is used in non-metallic flotation. The other alternative is an expensive anionic flotation-acid scrubbing-cationic flotation operation used for phosphate recovery as is described above.
It was discovered, that a saponified fatty acid concentrate could be cleaned one or more times and that the coarser fraction of the middlings could be screened away from the finer fraction leaving a high grade coarse middling that could report to the final concentrate, and a low grade fine middling that could either report to tailings or back to the head of the circuit. The resultant savings in reagent alone could amount to about $0.20/ton of originally mined crude ore and this would be in addition to the savings in. labor, and in the auxiliary capital equipment required for additional scrubbing, washing, conditioning and flotation.
In addition to the increased recovery of high grade phosphate product of the present process compared to the Florida Process, the capital and operating costs of the present process are drastically reduced because of (l) the elimination of the acid step for removing the anionic agent which reduces production costs by about 3.75 cents to 5.0 cents per ton of crude ore based on a cost of $25.00 per ton of H and (2) the elimination of the cationic reagent which reduces production costs by about 6.0 to 12.0 cents per ton of crude ore based on costs of about 30 cents per pound for the cationic reagents.
Based on the above and the present production figures for beneficiating Florida ores, the total reagent savings alone due to the elimination of the acid step would amount to about $1M; million per year and the savings due to the elimination of the cationic reagent would be about 513% million a year.
The process of the present invention will now be described with reference to the attached drawings in which:
FIG. 1 illustrates a flow diagram of one method of carrying out the process, and
FIG. 2 illustrates a second form of a flow diagram for carrying out the present invention.
FIG. 1 illustrates the process in which the phosphate ore as mined is first crushed to about 20 mesh and is then treated with water in a first scrubber l for about 2 minutes and then is subject to a screening 2 at about 20 mesh (Standard Tyler screen sizes). Any oversized material at about +20 mesh may be reground in a grinder 2a and returned to the scrubber while the undersize material at 20 mesh is fed to a deslimer 3. The desliming step may be carried out in cyclone separators or by very fine screens so as to effect a separation at about 500 mesh. The undersized material at about 500 mesh is slime and is discarded to waste. The oversized ore material having a size of +500 mesh is preferably passed to a second scrubber 4 and scrubbed for about 2 minutes and then passed to a second deslimer 5, the slime overflow from which may be recycled to the first deslimer. If found desirable for the particular ore being treated, the second scrubber 4 and second deslimer 5 may be eliminated so that the +500 mesh material from the first deslimer 3 may be passed directly to a sizing device. The sand material from deslimer 5 at about +500 mesh is diluted with water and the slurry passed through the sizing device or screen 6 to make a separation at about 100 mesh. The sizing device or screen 6 separates the deslimed ore into two fractions one comprising a coarse fraction of about by +100 mesh and the other a finer fraction of about -l00 by +500 mesh.
The coarser fraction is passed to a classifier 7 in which some of the water and possibly a small amount of fine particles is removed leaving an underflow sand fraction comprising about 75 percent solids. This fraction is passed to a drum conditioner 8 to which is added an anionic flotation reagent and certain other reagents to be described further hereinafter. After the ore material is thoroughly conditioned with the anionic flotation reagents it is passed to the rougher flotation cells 9. The flotation tailings, or underflow from the cells 9 are discarded along with other tailings as described further below. The flotation concentrate, without any further addition of reagents is passed to the cleaner flotation cells 10, the flotation tails from which are discarded and the flotation concentrate from which forms a portion of the final concentrate.
The finer fraction from screen 6 having a size of from l00 by +500 mesh is passed to a thickener 11. To this thickener may be added the overflow from classifier 7, if desired, and the overflow from the thickener 11 is removed for reuse in the process wherever dilution is called for as for example to scrubber l, deslimer S or sizing device 6. The ore pulp coming from the underflow of the thickener 11 comprises about 75 percent solids. This pulp is passed to drum conditioner 12 to which anionic flotation reagents are added as will be described further hereinafter. After this ore fraction has been thoroughly conditioned with the anionic reagents it is passed to the rougher flotation cells 13, the flotation tailings or underflow from which is discarded with the tailings from rougher flotation cells 9. The flotation concentrate, without any further addition of reagents is passed to cleaner flotation cells 14.. The cleaner flotation tailings from these cells are preferably recycled to the rougher flotation cells 13 for retreatment. The flotation concentrate from the cleaner flotation cells 14 without the addition of further reagents may be passed to recleaner flotation cells 15 for further upgrading and concentration of phosphate values in the ore. The flotation tails from the recleaner cells 15 are preferably recycled to the cleaner flotation cells 14 and the flotation concentrate is combined with the final concentrate from the cleaner flotation cells 10 obtained from the treatment of the coarse ore fraction.
According to FIG. 2, the same procedure is followed through elements 1 6 and the finer fraction, i.e. l00 by +500 mesh, is treated in the same fashion through elements 11 15. However, the coarser fraction, after passing through elements 7 9 is subjected to a different and more refined treatment. The tailings from the rougher flotation cells 9 are passed through a fine screen 16 which may be a DSM type screen provided with a knocking device to facilitate screening. If desirable the screen may be from about 28 mesh to about 65 mesh, and the oversized material is passed through a grinder 17 such as a wet hammer mill or rod mill and returned to the thickener 11 for the finer fraction, while the undersized material is passed to the final tailings. On the other hand, the concentrate from the rougher flotation cells 9 are passed, as before, to cleaner flotation cells 10. The tails therefrom are passed through a screen 18 of the types mentioned above for screen 16. The undersized fraction therefrom is recycled to the rougher flotation cells 9 or altematively passed with the material from grinder 17 to thickener 11, or, if desired, passed directly to final tailings. The oversized material is passed to the final concentrate. Whenever flotation cells have been referred to in the foregoing it will be understood that any group of such cells may, as is customary in the art, be referred to as flotation machines.
Whereever in this application mention is made of the use of screening as a sizing device this step may be car ried out by the use of a fixed, flat or curved screening surface, mounted on an incline, and of the Dutch State mines type of screen. To the rear side of the frame of the screen there may be attached a knocking device to prevent the screen from blinding.
With reference to FIG. 1 pertinent analyses of the various fractions throughout the process are shown in the following Table I:
TABLE I Product Weight B.P.L. covery B.P.L.
l. Calculated ore feed 100.00 24.69 100.00 2. 20 X l00 M Rougher cone. l9.76 71.52 57.27 3. Do. tails 20.48 4.59 3.78 4. Do. feed 40.24 37.46 6l.05 5. Do. cleaner cone. l7.82 76.87 55.46 6. D0. tlils [.94 22.48 L81 7. D0. feed l9.76 7l.52 57.27 8. [00 X 500 M Rougher conc. HA7 48.95 22.69 9. Do. tails 26.50 2.56 2.77
'. Do feed 37.97 16.56 25.46 11. Do. cleaner conc. 8.06 68.03 22.19 12. Do. tails 3.41 3.84 0.50 13. Do. feed 11.47 48.95 22.69 14. Do. Recleaner conc. 7.28 72.29 21.29 15. Do. tails 0.78 27.85 0.90 16. Do. feed 8.06 68.03 22.19
17. total flot. feed 78.21 27.31 86.51 18. total flot. cone. 25.10 75.54 76.75 19. total rougher tails 46.98 3.43 6.55 20. total cleaner-recleaner 6.13 12.82 3.21 tails 21. total slimes 21.79 15.29 13.49
With reference to FIG. 2 analyses of the various fractions are shown in the following Table 11:
TABLE 11 Re- Product Weight B.P.L. covery B.P.L. 1. Calculated ore feed 100.00 23.37 100.00 2. X 100 M Rougher cone. 14.77 80.61 50.95 3. a. Do. tails,+48M 7.01 5.29 1.73 b. Do. tails,-48M 0.94 6.99 0.30 4. Do. 1 feed 22.72 54.33 52.98 5. l00 X 500 M Rougher conc. 14.91 35.89 22.90 6. Do. tails 53.68 2.08 4.77 7. Do. feed 68.59 9.44 27.67 3. Do. cleaner cone. 8.69 57.82 21.46 9. Do. tails 6.22 5.42 1.44 10. Do. feed 14.91 35.89 22.90 11. Do. Recleaner cone. 7.90 62.50 21.16 12. Do. tails 0.79 8.87 .30 13. Do. feed 8.69 57.82 21.46 14. total flot. feed 84.54 21.82 78.91 15. total flot.conc. 22.67 74.27 72.11 16. total rougher tails 54.62 2.16 4.97 17. total cleaner-recleaner 7.01 5.92 1.74
tails 18. total slirnes 15.46 31.87 21.09
The various percentage values shown above are based on the original mined ore, and not, as is usually customary, on the deslimed ore as it is passed to the flotation cells.
it is to be noted that the'desliming steps are performed at about 500 mesh instead of the conventional 150-200 mesh and this has the immediate effect of reducing phosphate losses from about percent to about 15 20 percent.
Tne anionic reagents employed in the foregoing processes are comprised of fatty acid tall oil and fuel oil. While the ratio of fatty acid tall oil and fuel oil may vary within rather wide limits, the ratio is generally maintained at from about 1.5 to l to about 2.5 to 1. In Table 1 relating to FIG. 1, 4.9 lbs. of the fatty acid tall oil and 2.2 lbs of fuel oil were used per dry short ton of crude ore while in Table 11 relating to FIG. 2 the anionic reagents comprises 5.5 lbs. of fatty acid tall oil and 3.2 lbs. of fuel oil per dry short ton of crude ore.
it was found advantageous to flotation efficiencies in all respects to control the alkalinities of flotation feed pulps. The control was obtained by the addition of caustic soda, as required, to produce flotation feed pulps having pH values between about 7.5 and about 9.5. Sodium carbonate or lime could be used for the same purpose. 1
According to current practice, the Florida ores when subject to the anionic flotation-acid scrubbing-cationic flotation procedure commonly used as mentioned above give a final recovery of phosphate values from about 50 percent 60 percent based on the crude ore, whereas according to the present process the final recovery of phosphate values is in the range of 65 percent 80 percent.
1 claim:
l. A process for the beneficiation of phosphate ore comprising scrubbing the ores at least once, desliming the scrubbed ore at about 500 mesh after each of said at least one scrubbing steps, separating the deslimed ore at about 100 mesh to produce a coarse fraction and a fine fraction, passing the coarse fraction through a classifier to produce an overflow and a coarse slurry containing about percent solids, conditioning the coarse slurry with anionic flotation reagents, subjecting said conditioned coarse slurry to treatment in at least one rougher flotation machine to produce rougher tailings and a rougher concentrate, treating the concentrate in at least one cleaner flotation machine to produce tailings and a final concentrate, passing the fine fraction through a thickener to produce a time slurry containing about 75 percent solids, conditioning the fine slurry with anionic flotation reagents, subjecting the conditioned fine slurry to treatment in at least one rougher flotation machine to produce tailings and a concentrate, treating the concentrate in at least one cleaner flotation machine to produce tailings and a second concentrate, recycling said tailings to the at least one rougher flotation machine, treating the second concentrate in at least one recleaner flotation machine to produce tailings and a final concentrate, recycling the last mentioned tailings to the at least one cleaner flotation machine and combining the last mentioned concentrate with the final concentrate obtained from the coarse slurry and combining at least a portion of the tailings from the first mentioned. at least one rougher flotation machine with the tailing from the second mentioned at least one rougher flotation machine.
2. A process as claimed in claim 1 and further comprising screening at about 20 mesh the scrubbed ore, grinding the oversized material from said screening step and recyling said ground oversized material to said screening step and further comprising a second scrubbing step of the deslimed ore material and a second desliming step, the slime from said second desliming step being recycled to the first desliming step.
3. A process as claimed in claim 1 and further comprising passing the tailings from the at least one rougher flotation machine for the coarse slurry to a screening step having an effective mesh of separation from about 28 to about 65 mesh, passing the undersized material to final tailings, grinding the oversized material and passing the ground material to the thickener for the fine fraction.
4. A process as claimed in claim 3 and further comprising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screen having an effective mesh of separation from about 28 to about 65 mesh and recycling the undersized material to the at least one rougher flotation machine for the coarse fraction. 5. A process as claimed in claim 4 and further comprising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screen having an effective mesh of separation from about 28 to about 65 mesh and passing the undersized material to the thickener for the line fraction.
6. A process as claimed in claim 1 and further com prising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screening step on a fixed flat inclined or curved screen of the Dutch State mines type and to which is attached on the rear side of the frame of said screen a knocking device to prevent screen blinding and having an effective mesh ionic reagents comprise fatty acid tall oil and fuel oil in the ratio of from about 1.5 to l to about 2.5 to 1.0.
8. A process as claimed in claim. 1 wherein the said flotation operations are performed at controlled alkalinities wherein the pH of the flotation feed pulps are held between about 7.5 and about 9.5 with the use of caustic soda, lime or sodium carbonate.

Claims (7)

  1. 2. A process as claimed in claim 1 and further comprising screening at about 20 mesh the scrubbed ore, grinding the oversized material from said screening step and recyling said ground oversized material to said screening step and further comprising a second scrubbing step of the deslimed ore material and a second desliming step, the slime from said second desliming step being recycled to the first desliming step.
  2. 3. A process as claimed in claim 1 and further comprising passing the tailings from the at least one rougher flotation machine for the coarse slurry to a screening step having an effective mesh of separation from about 28 to about 65 mesh, passing the undersized material to final tailings, grinding the oversized material and passing the ground material to the thickener for the fine fraction.
  3. 4. A process as claimed in claim 3 and further comprising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screen having an effective mesh of separation from about 28 to about 65 mesh and recycling the undersized material to the at least one rougher flotation machine for the coarse fraction.
  4. 5. A process as claimed in claim 4 and further comprising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screen having an effective mesh of separation from about 28 to about 65 mesh and passing the undersized material to the thickener for the fine fraction.
  5. 6. A process as claimed in claim 1 and further comprising passing the tailings from the at least one cleaner flotation machine for the coarse fraction to a screening step on a fixed flat inclined or curved screen of the Dutch State mines type and to which is attached on the rear side of the frame of said screen a knocking device to prevent screen blinding and having an effective mesh of separation from about 28 mesh to about 65 mesh, and passing the oversize material to the final coarse concentrate fraction and the undersize to final tailings, or recycling the undersize fraction to the head of the coarse rougher flotation circuit or to the thickener at the head of the fine rougher flotation circuit.
  6. 7. A process as claimed in claim 1 wherein the anionic rEagents comprise fatty acid tall oil and fuel oil in the ratio of from about 1.5 to 1 to about 2.5 to 1.0.
  7. 8. A process as claimed in claim 1 wherein the said flotation operations are performed at controlled alkalinities wherein the pH of the flotation feed pulps are held between about 7.5 and about 9.5 with the use of caustic soda, lime or sodium carbonate.
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US4220523A (en) * 1978-07-19 1980-09-02 Jacobs Engineering Group Inc. Recovering of phosphates from phosphate ore
US4227996A (en) * 1979-03-22 1980-10-14 Celanese Corporation Flotation process for improving recovery of phosphates from ores
US4436616A (en) 1980-11-06 1984-03-13 Philippe Dufour Process for the beneficiation of phosphate ores
US4804462A (en) * 1988-04-18 1989-02-14 Lian-Yun-Gang Chemical Mines Research And Design Institute Beneficiating dolomitic phosphate ores with humic acid
US5865318A (en) * 1997-09-05 1999-02-02 Florida Institute Of Phosphate Research Reverse crago process for siliceous phosphates
CN100558467C (en) * 2007-02-06 2009-11-11 李东明 A kind of beneficiation method that improves brown iron ore grade
CN102773151A (en) * 2012-07-12 2012-11-14 云南磷化集团有限公司 Weathered collophanite graded processing technique
CN101632962B (en) * 2009-08-03 2013-01-16 孝义市天章铝业有限公司 Beneficiating method of diaspore type bauxite
CN104475270A (en) * 2014-12-29 2015-04-01 中蓝连海设计研究院 Mineral processing method of mechanical de-magging treating collophanite with additional medium
US20150182973A1 (en) * 2014-01-02 2015-07-02 Eriez Manufacturing Co. Material Processing System
EP3897994A4 (en) * 2018-12-18 2022-08-24 Metso Outotec Finland Oy Method and arrangement for process water treatment

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US4804462A (en) * 1988-04-18 1989-02-14 Lian-Yun-Gang Chemical Mines Research And Design Institute Beneficiating dolomitic phosphate ores with humic acid
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CN100558467C (en) * 2007-02-06 2009-11-11 李东明 A kind of beneficiation method that improves brown iron ore grade
CN101632962B (en) * 2009-08-03 2013-01-16 孝义市天章铝业有限公司 Beneficiating method of diaspore type bauxite
CN102773151B (en) * 2012-07-12 2013-12-11 云南磷化集团有限公司 Weathered collophanite graded processing technique
CN102773151A (en) * 2012-07-12 2012-11-14 云南磷化集团有限公司 Weathered collophanite graded processing technique
US20150182973A1 (en) * 2014-01-02 2015-07-02 Eriez Manufacturing Co. Material Processing System
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CN104475270A (en) * 2014-12-29 2015-04-01 中蓝连海设计研究院 Mineral processing method of mechanical de-magging treating collophanite with additional medium
CN104475270B (en) * 2014-12-29 2017-04-05 中蓝连海设计研究院 A kind of additional medium machinery de-magging processes the beneficiation method of collophane
EP3897994A4 (en) * 2018-12-18 2022-08-24 Metso Outotec Finland Oy Method and arrangement for process water treatment

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