US3773473A - Beneficiation and hot briquetting of phosphate ores by removing -400 mesh fines - Google Patents
Beneficiation and hot briquetting of phosphate ores by removing -400 mesh fines Download PDFInfo
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- US3773473A US3773473A US00870454A US3773473DA US3773473A US 3773473 A US3773473 A US 3773473A US 00870454 A US00870454 A US 00870454A US 3773473D A US3773473D A US 3773473DA US 3773473 A US3773473 A US 3773473A
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- shale
- phosphate
- fraction
- phosphorus
- calcined
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- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 42
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims abstract description 42
- 239000010452 phosphate Substances 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 claims description 20
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 27
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 27
- 239000011574 phosphorus Substances 0.000 abstract description 27
- 238000001354 calcination Methods 0.000 abstract description 18
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 239000007789 gas Substances 0.000 description 22
- 239000002245 particle Substances 0.000 description 18
- 239000004484 Briquette Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000002002 slurry Substances 0.000 description 10
- 239000007921 spray Substances 0.000 description 8
- 239000000446 fuel Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 3
- 239000012634 fragment Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000000915 furnace ionisation nonthermal excitation spectrometry Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002912 waste gas Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- GSWAOPJLTADLTN-UHFFFAOYSA-N oxidanimine Chemical compound [O-][NH3+] GSWAOPJLTADLTN-UHFFFAOYSA-N 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 239000002367 phosphate rock Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/01—Treating phosphate ores or other raw phosphate materials to obtain phosphorus or phosphorus compounds
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
Definitions
- a beneficiated, calcined, phosphate agglomerate, useful as a phosphorus furnace feed is produced by crushing phosphate shale to substantially inch, heating and calcining the crushed shale in a fluidized bed, removing a relatively phosphorus-poor fine fraction overhead from a relatively phosphorus-rich coarse fraction remaining in the fluidized bed, withdrawing a portion of the heated, coarse fraction from the fluidized bed and hot briquetting it under pressure to form strong, calcined phosphate agglomerates.
- phosphate ores obtainable in the western part of the United States are largely composed of phosphate shale containing up to about 32 percent P in the form of calcium phosphate. These ores also contain silica, iron oxide, organic matter, clay, small quantities of ammonium oxide and vanadium oxide and from 2 to 4 percent shale oil.
- One standard method for recovering the phosphorus from these ores is by reducing the phosphorus shale with carbon (coke) in an electric furnace.
- the phosphate ore must be fed into the electric furnace in the form of calcined lumps or calcined agglomerates in order to obtain smooth furnace operation during the conversion of the phosphate to phosphorus.
- the phosphate shale is crushed in a hammer mill into particulate form to pass a 4-inch screen.
- the crushed shale is then further screened into fine and coarse fractions using a 14 mm. screen, and the fine fraction is agglomerated by either briquetting or pelletizing; the agglomerated fraction and previously separated coarse fraction are then calcined together in a rotary kiln.
- a process has now been found for simultaneously beneficiating and calcining a phosphate ore to produce hard, calcined, phosphate agglomerates by crushing a phosphate ore to substantially inch, heating and calcining the crushed ore at a temperature of at least about l500F.
- the phosphate shale is initially ground or crushed by conventional means, such as an impact crusher, so that all of the shale is no larger than /fi inch in diameter.
- the crushing step is operated so that the maximum size of the crushed shale withdrawn is A inch in diameter; larger size lumps are recycled for additional crushing.
- large quantities of fines that is 325 mesh sized share, are desired (e.g., 20 to 40 percent) and obtained.
- grinding to a maximum size of 54; inch is necessary to obtain a high fines content in the crushed shale, and this is a preferred procedure when possible.
- the moist, crushed shale from the crusher is screened, and a inch fraction is passed to a rotating drum and blended with hot calcined briquettes from a source hereinafter described.
- the hot (at least 1500F.) briquettes are cooled by the moist shale, and the shale, in turn, is preheated in the rotating drum.
- Some portion, e.g., about 50 percent, of the moisture in the shale is evaporated during this preheating stage.
- the mixture of the crushed shale and the hot calcined briquettes is tumbled in the rotating drum until substantial extraction of heat from the briquette surfaces has occurred and the partially cooled briquettes can be handled on a conveyor belt surface. During this tumbling, the shale is also subject to further attrition, and more 325 mesh fines are generated in the rotating drum.
- the blend of calcined briquettes and crushed shale is then discharged onto a conveyor to allow additional contact time for heat transfer and then passed onto a 5% inch screen.
- the calcined briquettes being larger than /2 inch (they normally are about 1 /8 inches square), are removed as a inch product fraction, while the finer crushed shale falls through the screen.
- some briquette fragments also are removed in the /2 inch fraction. This screened, /2 inch fraction is then passed into a fluidized reactor where it is heated to calcining,
- particles of shale are suspended in a fluidized bed which is held up by the force of a fluidizing gas passing upwardly through the vertically disposed, tube-like, fluidized reactor.
- a fluidizing gas is a mixture of air and burnt fuel which both fluidizes the bed and also supplies the heat required to calcine the phosphate shale.
- temperatures on the order of at least 1500F. up to about 2200F. are employed in the bed. Temperatures substantially above 2200F. are not desirable since they cause the particles to soften and become sticky and to make fluidization difficult.
- the fluidizing gas is passed upwardly at a velocity sufficient to maintain the larger particles of the shale in the fluid bed while discharging overhead the -400 mesh fraction.
- the removal of these 400 mesh fines is esssential in the present process, since it has been found that the 400 fraction is substantially poorer in phosphorus values than is the +400 fraction. Accordingly, during the calcination stage in the fluidized bed'the substantially phosphorus-poor ore fraction, namely the 400 mesh fraction, is simultaneously removed, allowing both beneficiation and calcination of the shale to take place simultaneously.
- the +400 mesh ore particles are preferably heated to approximately 1800F. in the fluid bed to complete calcination during which organic matter and carbonates are decomposed.
- the resulting hot briquettes are then mixed with ground moist feed shale and passed into a rotating drum in a heat exchange relationship, as previously described. This permits the hot briquette to be cooled, and the feed shale to be preheated and partially dried prior to being fed into the fluidized reactor.
- the overhead gases and 400 mesh fines from the fluidized reactor are passed into a series of cyclone separators to remove the shale fines.
- the overhead gases from the cyclone separators are then passed through a spray tower containing lime to remove any fluoride which is evolved during the calcining stage; the resulting scrubbed gases, free of fluorides and shale particles, are then vented to the atmosphere.
- the shale be ground or crushed sufficiently fine so that a substantial portion of 325 mesh particles are generated during the crushing operation. Thereafter, when the ground shale is passed into the fluidized reactor, beneficiation of the ore results by removal of the -400 mesh fraction overhead from the fluidized reactor during calcination of the phosphate ore.
- the removal of the -400 fraction As a result of this discovery, the present process also contemplates selectively classifying from the overhead -3 25 mesh fines of the fluidized reactor, those particles which are in the range of 400 mesh, and returning these to the hot briquetting process where the amount of phosphorus which these fines contain justifies it.
- the finer material that is the 400 mesh, which invariably is substantially phosphorus-poor, is always removed from the fluidized reactor in order to beneficiate the remaining phosphate ore.
- phosphorus shale is passed by a conveyor 2 into a crusher 4, preferably an impact crusher, and ground to a size no larger than r inch.
- the crushed ore is then conveyed via conveyor 6 to a screen 8 having a size of no greater than k and preferably A inch.
- the inch fraction or oversized fraction is removed through line 12 and recycled back to the crusher 4, while the inch fraction is conveyed through conveyor 10 into rotating drum 14.
- the ground shale entering drum 14 is mixed with hot calcined briquettes from line 32 having a temperature of at least about 1500F., and they are tumbled together in the rotating drum 14.
- the hot calcined briquettes are cooled by contact with the ground, moist shale while the shale is preheated and partially dried (generally 50 percent of the moisture in the shale is evaporated) prior to being introduced into the fluidized reactor. Further, the tumbling in drum 14 attrites the shale and liberates more 325 shale particles from the ground shale. The resulting mixture is passed through conveyor 16 onto a 5% inch screen 18.
- the calcined briquettes which are greater than l inch in diameter, are removed through line 20 as product and passed on to an electric furnace, not shown.
- the inch fraction which is made up of the ground shale and briquette fragments, is then passed through line 22 into the fluidized reactor feed shute 23 of fluidized reactor 24.
- the shale fines enter the fluidized reactor 24, in which there is suspended a fluidized bed of ore particles, at a temperature of from about 1500F. to about 2200F.
- the fluidized bed is maintained in a fluidized state by passing heated air and combustible fuel up through the fluidized bed through line 66. This air and fuel mixture, on combustion, supply the heat necessary to maintain the fluid bed at the desired temperature.
- the fluidizing gas is passed through the fluidized bed at a rate sufficient to remove the 325 mesh ore fractions overhead through line 28, along with the products of combustion and other gaseous effluents which are given off during the calcining stage.
- the resulting, calcined ore particles which remain in the fluidized reactor 24 and which are at a temperature of at least 1500F., are then passed from exit port 26 in fluidized reactor 24 into the hot briquette press 30 equipped with press rolls 31.
- the hot calcined ore is briquetted under sufficient pressure to assure plastic flow of the ore during formation of the hard, adhesive briquettes.
- the hot calcined briquettes are then passed through line 32 into rotating drum 14, along with the crushed inch moist feed shale from line 10, as previously described.
- the overhead gases and 325 mesh fines which are removed through line 28 from the top of the fluidized bed pass into a cyclone separator or other conventional separating means 34 where the 325 +400 mesh particles are removed. If the phosphorus values of these particles are not sufficiently high, the particles are passed through line 38 into slurry tank 58. However, if the phosphorus values of this 325 +400 mesh fraction are sufficiently high, they may be conveyed through line 68 into the hot briquette press 30, along with the calcined shale from line 26 of fluidized reactor 24.
- the overhead gases and fines from cyclone separator 34 are then passed through line 36 into cyclone separator 40 where the remaining fine particles of phosphate shale are removed through lines 42, while the remaining gases are removed overhead through line 44 of the cyclone separator 40.
- the gases in line 44 are then passed into a spray tower 46 and are scrubbed with water to remove any fine particles of phosphate ore.
- any fluoride values which are evolved during the calcining stage are converted to insoluble calcium fluoride by passing lime through line 50 into the spray tower 46 in contact with the gases flowing through the spray tower 46.
- the precipitated fluoride and phosphate fines are removed through line 52 and passed into slurry tank 58.
- the resulting gases which are evolved from line 54 from the spray tower 46 are then passed into stack 56 where they are vented to the atmosphere.
- the contents of the rotating drum were screened on k inch screen 18, and the +56 inch fraction, which was all calcined briquette product, was removed via conveyor 20 to a phosphorus furnace. This product was removed at a rate of about 1 ton per hour and had a P 0 content of from 25 to 26 percent.
- the inch fraction which passed through screen 18 was essentially all ground shale and briquette fragments and were removed from screen 18 at a rate of 1.40 to 1.83 tons of shale per hour and 0072-0097 ton of water per hour and conveyed via conveyor 22 to the fluidized reactor inlet 23 of fluidized reactor 24.
- air was passed upwardly through the fluidized bed through line 66 at a rate of 20.8 to 27.8 thousand standard cubic feet per minute, while, simultaneously, natural gas was injected into the fluidized bed at a rate of 1020 t0 1360 standard cubic feet per minute.
- the resulting fluidized bed was maintained at a temperature of about 1800F. by means of the injected air and fuel.
- the 325 mesh solid shale particles were removed overhead at a rate of 0.29 to 0.73 ton of shale fines per hour, along with 0.072 to 0.097 ton of water vapor per hour, as well as decomposition gases. These were conveyed overhead from fluidized reactor 24 via conduit 28 to a first cyclone separator 34. Gases and -400 mesh shale fraction were removed via line 36 to a second cyclone separator 40, whie the 325 mesh to +400 mesh fraction was removed via line 38 and sent to slurry tank 58.
- the overhead gases were sent through line 44 to a spray tower 46 where they were scrubbed with water to remove any remaining fine shale particles. Further, the gases were treated with excess lime, introduced through line 50 into tower 46, to convert all fluoride gases which were evolved during the calcining reaction to insoluble calcium fluorides.
- the slurry from the base of the spray tower 46 was then conveyed through line 52 to slurry tank 58. The resulting scrubbed gases were then vented through line 54 and stack 56 at a rate of 0.06 to 0.8 ton of gases per hour.
- the calcined +325 mesh solids in the fluidized reactor 24 were removed through exit port 26 and conveyed to the hot briquette press 30 at a rate of about 1.1 tons per hour and there hot briquetted between rollers 30 and 31 at a temperature of about 1700F.
- the briquette press was equipped with a feed screw to create the additional pressures necessary for the hot briquetting operation. The temperature and pressure within the briquette press were sufficient to cause plastic flow of the shale during the briquetting operation.
- Make up water was added through line 48 into spray tower 46 and into slurry tank 58 at a rate sufficient to flow about 0.145 to 0.194 ton of water per hour to the settling pond 62 which was sufficient to remove 0.24 to 0.67 ton of shale fines per hour from the slurry tank 58. Recycle water from the settling pond 62 was removed and recycled through line 64 back to the slurry tank as was required.
- mine run shale having an average of 22 percent P 0 analysis 20-24 percent P 0 was beneficiated into a product containing 25-26 percent P 0 was beneficiated into a product containing 25-26 percent P 0 and the product was in the form of hard, calcined agglomerates which are eminently suitable for feed in a phosphorus furnace.
- a process for simultaneously beneficiating and calcining a phosphate ore to produce hard calcined phosphate agglomerates which comprises crushing a phosphate ore to substantially inch, heating and calcining the crushed ore at a temperature of at least about 1500F. in a fluidized bed, removing, without recycle a relatively phosphorus-poor, 400 mesh fraction overhead from a relatively phosphorus-rich fraction remaining in the fluidized bed, withdrawing hot, calcined, phosphorus-rich ore from said fluidized bed and briquetting said phosphorus-rich ore under sufficiently high pressures and temperatures to cause plastic flow of the ore, and recovering a calcined phosphate agglomerate suitable as a phosphorus furnace feed.
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Abstract
A beneficiated, calcined, phosphate agglomerate, useful as a phosphorus furnace feed is produced by crushing phosphate shale to substantially - 1/2 inch, heating and calcining the crushed shale in a fluidized bed, removing a relatively phosphorus-poor fine fraction overhead from a relatively phosphorus-rich coarse fraction remaining in the fluidized bed, withdrawing a portion of the heated, coarse fraction from the fluidized bed and hot briquetting it under pressure to form strong, calcined phosphate agglomerates.
Description
United States Patent Howard et al.
1451 Nov. 20, 1973 BENEFICIATION AND IIOT BRIQUETTING OF PHOSPHATE ORES BY REMOVING 400 MESH FINES Richard I. Howard; James K. Sullivan, both of Pocatello, Idaho FMC Corporation, New York, N.Y.
Oct. 2, 1969 Inventors:
Assignee:
Filed:
Appl. No.:
US. (:1 ..23/293 R, 23/312, 23/313, 71/44, 23/312 P, 75/26 Int. Cl C05b 19/00, B01 j 1/00 Field of Search 23/312 P, 223, 313, 23/293 R; 75/3, 26; 71/44 References Cited UNITED STATES PATENTS 7/1951 Hollingsworth 7 H44 2/1961 Stewart, Jr. et a1... 2/1963 Darrow et al 1. l/l968 I-lollingsworth et a1. 7/1970 Kass et al 71/44 FOREIGN PATENTS OR APPLICATIONS 7/ 1934 Norway 71/44 3/1952 Canada ..23/223 12/1963 Canada 75/26 OTHER PUBLICATIONS Elmore, et a.l., Deflourination of Phosphate Rock in the Molten State, Industrial & Eng. Chem., Jan.
Primary ExaminerNorman Yudkoff Assistant ExaminerR. T. Foster AztorneyFrank lanno and Eugene G. Seems [5 7 ABSTRACT A beneficiated, calcined, phosphate agglomerate, useful as a phosphorus furnace feed is produced by crushing phosphate shale to substantially inch, heating and calcining the crushed shale in a fluidized bed, removing a relatively phosphorus-poor fine fraction overhead from a relatively phosphorus-rich coarse fraction remaining in the fluidized bed, withdrawing a portion of the heated, coarse fraction from the fluidized bed and hot briquetting it under pressure to form strong, calcined phosphate agglomerates.
3 Claims, 1 Drawing Figure SHALE FEE D T SCRUBED VENT GASES I 54 5G I MAKE UP WATER -48 AT/wt ,LIME 44 +1/2" FRACTION 14 m DRUMTING 16 a HOT CALCINED -1/2"FRAcr10N BRIQUETTES 22 IIZ'CALCINED BRIQUETTES PRODUCT RECYCLE SETTLING POND REACTOR 66 AIR l I GAS FUEL HOT BRIOUET TE PRESS BENEFICIAT-ION AND ,HOT BRIQUETTING OF Y PHOSPHATE ORES BY REMOVING 400 MESH FINES BACKGROUND or THE INVENTION 1. Field of the Invention The invention relates to a process for producing calcined phosphate agglomerates which are especially suitable for use as furnace feeds in the manufacture of phosphorus.
2. Description of the Prior Art The phosphate ores obtainable in the western part of the United States are largely composed of phosphate shale containing up to about 32 percent P in the form of calcium phosphate. These ores also contain silica, iron oxide, organic matter, clay, small quantities of ammonium oxide and vanadium oxide and from 2 to 4 percent shale oil. One standard method for recovering the phosphorus from these ores is by reducing the phosphorus shale with carbon (coke) in an electric furnace. The phosphate ore must be fed into the electric furnace in the form of calcined lumps or calcined agglomerates in order to obtain smooth furnace operation during the conversion of the phosphate to phosphorus. To produce a suitable furnace feed, the phosphate shale is crushed in a hammer mill into particulate form to pass a 4-inch screen. The crushed shale is then further screened into fine and coarse fractions using a 14 mm. screen, and the fine fraction is agglomerated by either briquetting or pelletizing; the agglomerated fraction and previously separated coarse fraction are then calcined together in a rotary kiln. An improvement in the above process is obtained by carrying out the calcination of the agglomerated fines into briquettes, and the coarse fraction (which is normally termed lump) into calcined lumps, on a perforated, non-agitated carrier; this generates less fines, and the non-agitated calcination forms stronger briquettes.
One of the difficulties that has arisen in the above process is that the amount of high grade shale, that is shale containing over 28 percent P 0 which is available is rapidly decreasing, and reliance for phosphate supplies has had to be limited to the so-called furnace grade shale (P 0 content of from 22 to 28 percen by weight). and low-grade shale (P 0 content of below 22 percent by weight). While furnace grade shale is acceptable and in use, it is desired to increase its P 0 content for more efficient operation. Even more desirable is a process that can utilize the low-grade (also termed mill grade) phosphate ore which contains less than 22 percent P 0 However, in the present furnaces the attempted use of feeds having phosphorus concentrations lower than 22 percent P 0 makes furnace operations difficult and is uneconomical to use by conventionally knowntechniques.
The beneficiation of these ores has been attempted prior to the shale being treated in the conventional calcining and briquetting operations; however, the cost of the additional beneficiation step at this time does not warrant its use. As a result, large quantities of lowgrade ore simply cannot be utilized, per se, in the present furnaces. Accordingly, what is desired is a process which will permit calcined phosphate agglomerates to be produced from low-grade ore without the need for special beneficiation steps. Further, such a process should also be capable of utilizing furnace-grade ores While pg a i IMP- 5. s nteaie the 5? calmed briquette. In this way, beneficiation can be effectively achieved without the cost of running separate beneficiation stages.
SUMMARY OF THE INVENTION A process has now been found for simultaneously beneficiating and calcining a phosphate ore to produce hard, calcined, phosphate agglomerates by crushing a phosphate ore to substantially inch, heating and calcining the crushed ore at a temperature of at least about l500F. in a fluidized bed, removing a relatively phosphorus-poor, 400 mesh fraction overhead from a relatively phosphorus-rich fraction remaining in the fluidized bed, withdrawing hot, calcined, phosphorusrich ore from the fluidized bed and briquetting it under a sufficiently high pressure and temperature to cause plastic flow of the ore, and recovering a hard, calcined phosphate agglomerate suitable as a phosphorus furnace feed.
BRIEF DESCRIPTION OF THE DRAWING In the drawing there is illustrated a schematic representation of one embodiment for carrying out the present invention.
DESCRIPTION OF THE INVENTION AND THE PREFERRED EMBODIMENTS In carrying out the present invention, the phosphate shale is initially ground or crushed by conventional means, such as an impact crusher, so that all of the shale is no larger than /fi inch in diameter. The crushing step is operated so that the maximum size of the crushed shale withdrawn is A inch in diameter; larger size lumps are recycled for additional crushing. In this operation large quantities of fines, that is 325 mesh sized share, are desired (e.g., 20 to 40 percent) and obtained. In many instances, grinding to a maximum size of 54; inch is necessary to obtain a high fines content in the crushed shale, and this is a preferred procedure when possible.
The moist, crushed shale from the crusher is screened, and a inch fraction is passed to a rotating drum and blended with hot calcined briquettes from a source hereinafter described. Upon being tumbled in the rotating drum, the hot (at least 1500F.) briquettes are cooled by the moist shale, and the shale, in turn, is preheated in the rotating drum. Some portion, e.g., about 50 percent, of the moisture in the shale is evaporated during this preheating stage. The mixture of the crushed shale and the hot calcined briquettes is tumbled in the rotating drum until substantial extraction of heat from the briquette surfaces has occurred and the partially cooled briquettes can be handled on a conveyor belt surface. During this tumbling, the shale is also subject to further attrition, and more 325 mesh fines are generated in the rotating drum.
The blend of calcined briquettes and crushed shale is then discharged onto a conveyor to allow additional contact time for heat transfer and then passed onto a 5% inch screen. The calcined briquettes, being larger than /2 inch (they normally are about 1 /8 inches square), are removed as a inch product fraction, while the finer crushed shale falls through the screen. In addition to crushed shale, some briquette fragments also are removed in the /2 inch fraction. This screened, /2 inch fraction is then passed into a fluidized reactor where it is heated to calcining,
temperatures.
In the fluidized reactor, particles of shale are suspended in a fluidized bed which is held up by the force of a fluidizing gas passing upwardly through the vertically disposed, tube-like, fluidized reactor. In the normal procedure the upflowing, fluidizing gas is a mixture of air and burnt fuel which both fluidizes the bed and also supplies the heat required to calcine the phosphate shale. Normally, temperatures on the order of at least 1500F. up to about 2200F. are employed in the bed. Temperatures substantially above 2200F. are not desirable since they cause the particles to soften and become sticky and to make fluidization difficult.
Within the fluidized bed the fluidizing gas is passed upwardly at a velocity sufficient to maintain the larger particles of the shale in the fluid bed while discharging overhead the -400 mesh fraction. The removal of these 400 mesh fines is esssential in the present process, since it has been found that the 400 fraction is substantially poorer in phosphorus values than is the +400 fraction. Accordingly, during the calcination stage in the fluidized bed'the substantially phosphorus-poor ore fraction, namely the 400 mesh fraction, is simultaneously removed, allowing both beneficiation and calcination of the shale to take place simultaneously. The +400 mesh ore particles are preferably heated to approximately 1800F. in the fluid bed to complete calcination during which organic matter and carbonates are decomposed.
The hot calcined shale, while at substantially the same temperature as the shale in the fluidized bed, is
then passed into a hot briquette press and briquetted,
beneflciates the remaining ore because this fraction contains substantially less phosphorus values than do the larger phosphate shale particles, namely, the +400 mesh fraction. The separation of the phosphate fines, which are phosphorus-poor, from the larger fraction which is substantially phosphorus-rich, is an essential feature of the instant process. This can readily be observed by typical analysis of various samples of shale ore as set forth in Table I.
TABLE I.PHOSPHATE SHALE SAMPLE ANALYSIS P205 Percent concentra- Percent of total Wt. percent tion in P205 P20 P20 recovered -325M in starting in in in +325M Sample the shale 1 material -325M +325M fraction In addition, if the 325 mesh phosphorus ore fraction is analyzed, it is found that the coarser fraction within the 325 mesh fraction contains substantially more P 0 than the fine fraction. For example the -3 mesh to +400 mesh fraction contains substantially more phosphorus than does the 400 mesh to the 5 micron and the particles lower than 5 micron. This is illustrated in Table II.
TABLE II.-P2O5 DISTRIBUTION WITHIN THE MINUS 325 MESH FRACTION OF PHOSPHATE SHALE ORES =Weight percent of original shale.
while hot, at sufficiently high pressures so that there is plastic flow of the phosphate ore at the temperature at which the briquette is formed. this insures a dense, hard briquette whose contents are strongly adhered to one another. The resulting hot briquettes are then mixed with ground moist feed shale and passed into a rotating drum in a heat exchange relationship, as previously described. This permits the hot briquette to be cooled, and the feed shale to be preheated and partially dried prior to being fed into the fluidized reactor.
The overhead gases and 400 mesh fines from the fluidized reactor are passed into a series of cyclone separators to remove the shale fines. The overhead gases from the cyclone separators are then passed through a spray tower containing lime to remove any fluoride which is evolved during the calcining stage; the resulting scrubbed gases, free of fluorides and shale particles, are then vented to the atmosphere.
In the present process it is essential that the shale be ground or crushed sufficiently fine so that a substantial portion of 325 mesh particles are generated during the crushing operation. Thereafter, when the ground shale is passed into the fluidized reactor, beneficiation of the ore results by removal of the -400 mesh fraction overhead from the fluidized reactor during calcination of the phosphate ore. The removal of the -400 fraction As a result of this discovery, the present process also contemplates selectively classifying from the overhead -3 25 mesh fines of the fluidized reactor, those particles which are in the range of 400 mesh, and returning these to the hot briquetting process where the amount of phosphorus which these fines contain justifies it. The finer material, that is the 400 mesh, which invariably is substantially phosphorus-poor, is always removed from the fluidized reactor in order to beneficiate the remaining phosphate ore.
The invention will now be described with reference to the attached drawing. In the drawing, phosphorus shale is passed by a conveyor 2 into a crusher 4, preferably an impact crusher, and ground to a size no larger than r inch. The crushed ore is then conveyed via conveyor 6 to a screen 8 having a size of no greater than k and preferably A inch. The inch fraction or oversized fraction is removed through line 12 and recycled back to the crusher 4, while the inch fraction is conveyed through conveyor 10 into rotating drum 14. The ground shale entering drum 14 is mixed with hot calcined briquettes from line 32 having a temperature of at least about 1500F., and they are tumbled together in the rotating drum 14.
The tumbling of this mixed feed in drum 14 achieves two desirable results. Initially, the hot calcined briquettes are cooled by contact with the ground, moist shale while the shale is preheated and partially dried (generally 50 percent of the moisture in the shale is evaporated) prior to being introduced into the fluidized reactor. Further, the tumbling in drum 14 attrites the shale and liberates more 325 shale particles from the ground shale. The resulting mixture is passed through conveyor 16 onto a 5% inch screen 18. The calcined briquettes, which are greater than l inch in diameter, are removed through line 20 as product and passed on to an electric furnace, not shown. The inch fraction, which is made up of the ground shale and briquette fragments, is then passed through line 22 into the fluidized reactor feed shute 23 of fluidized reactor 24.
The shale fines enter the fluidized reactor 24, in which there is suspended a fluidized bed of ore particles, at a temperature of from about 1500F. to about 2200F. The fluidized bed is maintained in a fluidized state by passing heated air and combustible fuel up through the fluidized bed through line 66. This air and fuel mixture, on combustion, supply the heat necessary to maintain the fluid bed at the desired temperature. The fluidizing gas is passed through the fluidized bed at a rate sufficient to remove the 325 mesh ore fractions overhead through line 28, along with the products of combustion and other gaseous effluents which are given off during the calcining stage. The resulting, calcined ore particles which remain in the fluidized reactor 24 and which are at a temperature of at least 1500F., are then passed from exit port 26 in fluidized reactor 24 into the hot briquette press 30 equipped with press rolls 31. In this press 30 the hot calcined ore is briquetted under sufficient pressure to assure plastic flow of the ore during formation of the hard, adhesive briquettes. The hot calcined briquettes are then passed through line 32 into rotating drum 14, along with the crushed inch moist feed shale from line 10, as previously described.
The overhead gases and 325 mesh fines which are removed through line 28 from the top of the fluidized bed pass into a cyclone separator or other conventional separating means 34 where the 325 +400 mesh particles are removed. If the phosphorus values of these particles are not sufficiently high, the particles are passed through line 38 into slurry tank 58. However, if the phosphorus values of this 325 +400 mesh fraction are sufficiently high, they may be conveyed through line 68 into the hot briquette press 30, along with the calcined shale from line 26 of fluidized reactor 24. The overhead gases and fines from cyclone separator 34 are then passed through line 36 into cyclone separator 40 where the remaining fine particles of phosphate shale are removed through lines 42, while the remaining gases are removed overhead through line 44 of the cyclone separator 40. The gases in line 44 are then passed into a spray tower 46 and are scrubbed with water to remove any fine particles of phosphate ore. Additionally, any fluoride values which are evolved during the calcining stage are converted to insoluble calcium fluoride by passing lime through line 50 into the spray tower 46 in contact with the gases flowing through the spray tower 46. The precipitated fluoride and phosphate fines are removed through line 52 and passed into slurry tank 58. The resulting gases which are evolved from line 54 from the spray tower 46 are then passed into stack 56 where they are vented to the atmosphere.
sult in increasing the P 0 analysis of the ore as much as 14 percentage units, depending -on the P P 0 contents of the starting ore and of the P 0 of the 3 25 mesh fraction. Moreover, while the present process obviously has its greatest advantage in beneficiating the low grade ores into higher grade phosphate ores, it should be realized that this beneficiating stage can be used to upgrade the phosphorus values of most ores, including furnace grade ores, since the 400 fines fraction is substantially poorer in phosphate values than is the coarser +400 mesh fraction.
The following example is given to illustrate the invention and is not deemed to be limiting thereof.
EXAMPLE The equipment used in carrying out the present example was the same as illustrated in the drawing, and for claritys sake the example will be explained with reference to the drawing. A mine run shale having a P 0 content of from 20 to 24 percent (average 22 percent) was fed along with 10 percent by weight of water to an impact crusher 4 at a rate varying from 1.45 to 1.94 tons per hour. The crushed product was then conveyed by means 6 to a A inch screen 8, and the Ainch fraction, which comprised about 1.31 to 1.74 tons of shale per hour and 0.145 to 0.194 ton of water per hour, were conveyed by conveyor 10 to a heat exchange and attrition drum 14. The remaining oversize shale was recycled back to the crusher for additional grinding.
To the /z inch ground shale in drum 14 were also added hot calcined briquettes from hot briquette press 30 through line 32 at a rate of about 1.10 tons of briquettes per hour. These were placed in the rotating drum 114, and the briquettes and the moist shale were then tumbled in drum 14 until substantial heat exchange had taken place. The drum spill was removed through conveyor 16 to a 4 inch screen 18. Dust and fumes which were given off from the rotating drum 14 were removed and sent to slurry tank 58 by means not shown. This dust removed from drum l4 amounted to about 0.013 to 0.019 ton of shale fines per hour and 0.073 to 0.097 ton of water per hour. The contents of the rotating drum were screened on k inch screen 18, and the +56 inch fraction, which was all calcined briquette product, was removed via conveyor 20 to a phosphorus furnace. This product was removed at a rate of about 1 ton per hour and had a P 0 content of from 25 to 26 percent. The inch fraction which passed through screen 18 was essentially all ground shale and briquette fragments and were removed from screen 18 at a rate of 1.40 to 1.83 tons of shale per hour and 0072-0097 ton of water per hour and conveyed via conveyor 22 to the fluidized reactor inlet 23 of fluidized reactor 24. In the fluidized reactor 24 air was passed upwardly through the fluidized bed through line 66 at a rate of 20.8 to 27.8 thousand standard cubic feet per minute, while, simultaneously, natural gas was injected into the fluidized bed at a rate of 1020 t0 1360 standard cubic feet per minute. The resulting fluidized bed was maintained at a temperature of about 1800F. by means of the injected air and fuel.
In the fluidized reactor 24 the 325 mesh solid shale particles were removed overhead at a rate of 0.29 to 0.73 ton of shale fines per hour, along with 0.072 to 0.097 ton of water vapor per hour, as well as decomposition gases. These were conveyed overhead from fluidized reactor 24 via conduit 28 to a first cyclone separator 34. Gases and -400 mesh shale fraction were removed via line 36 to a second cyclone separator 40, whie the 325 mesh to +400 mesh fraction was removed via line 38 and sent to slurry tank 58. On occasion where the P content of the fines fraction from cyclone separator 34 was sufficiently high grade, a portion of the fines was returned via line 68 to the hot briquette press 30. The -325 +400 mesh fraction removed from the first cyclone 34 separator was removed at a rate of 0.05 to 0.07 ton of shale fines per hour. The waste gases and 400 mesh particles which were conveyed to the second cyclone separator 40 through line 36 were then separated into substantially waste gases and into remaining shale fines. The remaining shale fines weighing 0.18 to 0.58 ton of shale per hour were sent via line 42 to the slurry tank 58. The overhead gases were sent through line 44 to a spray tower 46 where they were scrubbed with water to remove any remaining fine shale particles. Further, the gases were treated with excess lime, introduced through line 50 into tower 46, to convert all fluoride gases which were evolved during the calcining reaction to insoluble calcium fluorides. The slurry from the base of the spray tower 46 was then conveyed through line 52 to slurry tank 58. The resulting scrubbed gases were then vented through line 54 and stack 56 at a rate of 0.06 to 0.8 ton of gases per hour.
The calcined +325 mesh solids in the fluidized reactor 24 were removed through exit port 26 and conveyed to the hot briquette press 30 at a rate of about 1.1 tons per hour and there hot briquetted between rollers 30 and 31 at a temperature of about 1700F. The briquette press was equipped with a feed screw to create the additional pressures necessary for the hot briquetting operation. The temperature and pressure within the briquette press were sufficient to cause plastic flow of the shale during the briquetting operation. Make up water was added through line 48 into spray tower 46 and into slurry tank 58 at a rate sufficient to flow about 0.145 to 0.194 ton of water per hour to the settling pond 62 which was sufficient to remove 0.24 to 0.67 ton of shale fines per hour from the slurry tank 58. Recycle water from the settling pond 62 was removed and recycled through line 64 back to the slurry tank as was required.
As a result of the above example, mine run shale having an average of 22 percent P 0 (analysis 20-24 percent P 0 was beneficiated into a product containing 25-26 percent P 0 was beneficiated into a product containing 25-26 percent P 0 and the product was in the form of hard, calcined agglomerates which are eminently suitable for feed in a phosphorus furnace.
Pursuant to the requirements of the patent statutes, the principle of this invention has been explained and exemplified in a manner so that it can be readily practiced by those skilled in the art, such exemplification including what is considered to represent the best embodiment of the invention. However, it should be clearly understood that, within the scope of the appended claims, the invention may be practiced by those skilled in the art, and having the benefit of this disclousre otherwise than as specifically described and exemplified herein.
What is claimed is:
1. A process for simultaneously beneficiating and calcining a phosphate ore to produce hard calcined phosphate agglomerates which comprises crushing a phosphate ore to substantially inch, heating and calcining the crushed ore at a temperature of at least about 1500F. in a fluidized bed, removing, without recycle a relatively phosphorus-poor, 400 mesh fraction overhead from a relatively phosphorus-rich fraction remaining in the fluidized bed, withdrawing hot, calcined, phosphorus-rich ore from said fluidized bed and briquetting said phosphorus-rich ore under sufficiently high pressures and temperatures to cause plastic flow of the ore, and recovering a calcined phosphate agglomerate suitable as a phosphorus furnace feed.
2. Process of claim 1 wherein the fluidized bed is maintained at a temperature of from about 1500F. to about 2200F.
3. Process of claim 1 wherein substantially all of the phosphate ore is crushed to inch in diameter.
Claims (2)
- 2. Process of claim 1 wherein the fluidized bed is maintained at a temperature of from about 1500*F. to about 2200*F.
- 3. Process of claim 1 wherein substantially all of the phosphate ore is crushed to - 1/4 inch in diameter.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87045469A | 1969-10-02 | 1969-10-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3773473A true US3773473A (en) | 1973-11-20 |
Family
ID=25355410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00870454A Expired - Lifetime US3773473A (en) | 1969-10-02 | 1969-10-02 | Beneficiation and hot briquetting of phosphate ores by removing -400 mesh fines |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3773473A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4249906A (en) * | 1979-12-17 | 1981-02-10 | Howell Phillip C | Method and apparatus for handling flux fines |
| WO1982002724A1 (en) * | 1981-02-05 | 1982-08-19 | Phillip C Howell | Method and apparatus for handling flux fines |
| EP0215210A1 (en) * | 1985-08-14 | 1987-03-25 | Thyssen Stahl Aktiengesellschaft | Process and installation for preparing binder-free hot-briquets |
| US4783328A (en) * | 1987-12-14 | 1988-11-08 | Fmc Corporation | Utilization of phosphourus containing by-products |
| US4806326A (en) * | 1987-08-17 | 1989-02-21 | Fmc Corporation | Phosphate feed material for phosphorus electric furnace |
| US4822583A (en) * | 1987-08-17 | 1989-04-18 | Fmc Corporation | Phosphate feed material for phosphorus electric furnaces and production of same |
| US20090165516A1 (en) * | 2005-12-29 | 2009-07-02 | Petroleo Brasileiro S.A. - Petrobras | Process for obtaining a fertilizer with sustained release of phosphorus |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2562718A (en) * | 1947-10-18 | 1951-07-31 | Coronet Phosphate Company | Defluorination of phosphate rock |
| CA481706A (en) * | 1952-03-11 | Shawinigan Chemicals Limited | Briquetting | |
| US2971832A (en) * | 1955-12-06 | 1961-02-14 | Int Minerals & Chem Corp | Granulation of mixed fertilizers |
| US3076248A (en) * | 1960-11-17 | 1963-02-05 | Fmc Corp | Process for the production of calcined phosphate agglomerates |
| CA676711A (en) * | 1963-12-24 | Arthur D. Little | Process for gas reduction of iron oxides using a reformed hydrocarbon | |
| US3364008A (en) * | 1965-03-19 | 1968-01-16 | Borden Co | Method of defluorinating phosphate rock in a fluidized bed reactor |
| US3522338A (en) * | 1968-05-31 | 1970-07-28 | Fmc Corp | Method for hot briquetting calcium phosphate ore |
-
1969
- 1969-10-02 US US00870454A patent/US3773473A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA481706A (en) * | 1952-03-11 | Shawinigan Chemicals Limited | Briquetting | |
| CA676711A (en) * | 1963-12-24 | Arthur D. Little | Process for gas reduction of iron oxides using a reformed hydrocarbon | |
| US2562718A (en) * | 1947-10-18 | 1951-07-31 | Coronet Phosphate Company | Defluorination of phosphate rock |
| US2971832A (en) * | 1955-12-06 | 1961-02-14 | Int Minerals & Chem Corp | Granulation of mixed fertilizers |
| US3076248A (en) * | 1960-11-17 | 1963-02-05 | Fmc Corp | Process for the production of calcined phosphate agglomerates |
| US3364008A (en) * | 1965-03-19 | 1968-01-16 | Borden Co | Method of defluorinating phosphate rock in a fluidized bed reactor |
| US3522338A (en) * | 1968-05-31 | 1970-07-28 | Fmc Corp | Method for hot briquetting calcium phosphate ore |
Non-Patent Citations (1)
| Title |
|---|
| Elmore, et al., Deflourination of Phosphate Rock in the Molten State, Industrial & Eng. Chem., Jan. 1942, pp. 40 48. * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4249906A (en) * | 1979-12-17 | 1981-02-10 | Howell Phillip C | Method and apparatus for handling flux fines |
| WO1982002724A1 (en) * | 1981-02-05 | 1982-08-19 | Phillip C Howell | Method and apparatus for handling flux fines |
| EP0215210A1 (en) * | 1985-08-14 | 1987-03-25 | Thyssen Stahl Aktiengesellschaft | Process and installation for preparing binder-free hot-briquets |
| US4806326A (en) * | 1987-08-17 | 1989-02-21 | Fmc Corporation | Phosphate feed material for phosphorus electric furnace |
| US4822583A (en) * | 1987-08-17 | 1989-04-18 | Fmc Corporation | Phosphate feed material for phosphorus electric furnaces and production of same |
| US4783328A (en) * | 1987-12-14 | 1988-11-08 | Fmc Corporation | Utilization of phosphourus containing by-products |
| US20090165516A1 (en) * | 2005-12-29 | 2009-07-02 | Petroleo Brasileiro S.A. - Petrobras | Process for obtaining a fertilizer with sustained release of phosphorus |
| US8034149B2 (en) * | 2005-12-29 | 2011-10-11 | Petroleo Brasileiro S.A.-Petrobras | Process for obtaining a fertilizer with sustained release of phosphorus |
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