US2259420A - Flotation process for oxidized manganese ore - Google Patents
Flotation process for oxidized manganese ore Download PDFInfo
- Publication number
- US2259420A US2259420A US254007A US25400739A US2259420A US 2259420 A US2259420 A US 2259420A US 254007 A US254007 A US 254007A US 25400739 A US25400739 A US 25400739A US 2259420 A US2259420 A US 2259420A
- Authority
- US
- United States
- Prior art keywords
- ore
- talloel
- pulp
- flotation
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 238000005188 flotation Methods 0.000 title description 38
- 238000000034 method Methods 0.000 title description 31
- 230000008569 process Effects 0.000 title description 26
- 239000011572 manganese Substances 0.000 title description 24
- 229910052748 manganese Inorganic materials 0.000 title description 21
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 35
- 229910052500 inorganic mineral Inorganic materials 0.000 description 26
- 239000011707 mineral Substances 0.000 description 26
- 235000010755 mineral Nutrition 0.000 description 25
- 239000006185 dispersion Substances 0.000 description 21
- 239000003153 chemical reaction reagent Substances 0.000 description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000003921 oil Substances 0.000 description 18
- 239000000839 emulsion Substances 0.000 description 17
- 238000000227 grinding Methods 0.000 description 17
- 239000012141 concentrate Substances 0.000 description 16
- 239000002245 particle Substances 0.000 description 14
- 239000000463 material Substances 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 239000000344 soap Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 239000003995 emulsifying agent Substances 0.000 description 9
- 230000007935 neutral effect Effects 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000003518 caustics Substances 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229940049964 oleate Drugs 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 5
- 239000000084 colloidal system Substances 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 229960004418 trolamine Drugs 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000012459 cleaning agent Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WGIMXKDCVCTHGW-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCCO WGIMXKDCVCTHGW-UHFFFAOYSA-N 0.000 description 1
- PWVUXRBUUYZMKM-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCO PWVUXRBUUYZMKM-UHFFFAOYSA-N 0.000 description 1
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 1
- JZSMZIOJUHECHW-GTJZZHROSA-N 2-hydroxypropyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(C)O JZSMZIOJUHECHW-GTJZZHROSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910000616 Ferromanganese Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical class COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 229940031768 diglycol stearate Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- CNZOFNMWZBNPLL-OSKRVHINSA-L flot regimen Chemical compound [Pt+4].[O-]C(=O)C([O-])=O.[NH-][C@H]1CCCC[C@@H]1[NH-].FC1=CNC(=O)NC1=O.O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)C(O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 CNZOFNMWZBNPLL-OSKRVHINSA-L 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- -1 hydrocarbon sulphonate Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION 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
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/02—Froth-flotation processes
Definitions
- the present invention relates to flotation procfrom the gangue in order that a flotation separaesses and flotation reagents for use in the seption may be effected.
- the tendency for talloel aration of minerals, with particular reference to soap, or talloel in highly alkaline pulps, to give the concentration of oxidized metallic ores, such 7 avoluminous tenacious froth is even more serious I as the oxidized ores of manganese. 1 when both the ore and gangue materials have It is an object'of my invention to provide a pronounced sliming characteristics.
- the low flotation process which gives improved recovergrade manganese ores of Eastern Cuba are a ies and higher grade concentrates, at lower costs notable example of this type of ore.
- Sliming of operation, in the flotation of oxidized metallic ores are especially hard to concentrate with talores.
- Another object of my invention is to provide 4 alkaline pulps, because the slime, much of which flotation reagents which are cheaper and more may extend into the true colloidal range, tends easily prepared than any now known in the art. to stabilize the froth. This tendency of slime
- Another object of the invention is to provide to stabilizethe froth is especially marked in a flotation process which gives efficient recovl5 pulps of high alkalinity.
- Classiwatery pulp of the or the tanoel is added to flcationto any selected size range before flotation an ore pulp which has been made alkaline w naturally increases the loss of valuable minerals a suitable caustic agent, thereby forming the in the fine sizes and when both the ore and Soap Sit? the amount of caustic beingreg' 40 gangue minera1s have a tendency to slime the mated to maintain high degree of alkalinity in losses make such treatment economically im- 'the pulp 'after-themddition ot- .the talloel.
- drocarbon oil such as gas 'oil'pr fue'l oihalong more than pH 7.4.
- the oil may be emulsified with the talloel, added to the grind separately, or fed in stages to the various flotation cells. I have found that especially good results are obtained where at least a part of the neutral hydrocarbon oil is fed these results may be obtained when treating pulps of diverse qualities without encountering the restrictive and costly requirements involved in the use of the known processes.
- talloel any type of talloel can be used effectively, the gravity, acid number, iodine num ber, etc, beihg relatively unimportant.
- a purified talloel "the material produced by simple acidulation'of. crude black liquor soap being entirely suitable.
- the lignins, etc., present in this material simply act as harmless diluents.
- oxidized metallic ores such as oxidized ores of manganese
- a dispersion of talloel in water, constituting the flotation reagent is prepared by mixing; the talloel and water in the presence of a small amount of emulsifying agent, which may be an added organic, neutral, oil-soluble'or water-soluble material, or a material produced in situ by the addition of a small amount of an organic talloel-soluble base or an inorganic watersoluble base, depending upon the procedure selected for preparing the dispersion.
- emulsifying agent which may be an added organic, neutral, oil-soluble'or water-soluble material, or a material produced in situ by the addition of a small amount of an organic talloel-soluble base or an inorganic watersoluble base, depending upon the procedure selected for preparing the dispersion.
- the coarsely crushed ore is fed to a rod or ball mill operating in closed circuit with a mechanical classifier for returning insufficiently ground material to the mill.
- a mechanical classifier for returning insufficiently ground material to the mill.
- water and the emulsified talloel reagent are added to theorem the -properf.preportions. Ihavefound that best results are secured when the water content is ad-- justed to such an amount that the solids represent from about 20 to 35% of the total mass of the pulp. I have further found that best results gives good results.
- the ore minerals particles are levitated to the surface of the pulp by attachment to the air bubbles introduced into the pulp.
- the ore minerals become preferentially attached to the air bubbles due to the fact that the emulsified talloel reagent selectively .coats the surfaces of the ore minerals with a water repellent, nonpolar film which has a greater affinity for the'air than for water, the gangue minerals being entirely unaffected by the treatment.
- The-mineral laden bubbles, or concentrate is collected as a froth on the surface of the pulp; the gangue minerals, being unaffected by the presence of the emulsified talloel reagent, remain wetted by the water of the pulp, sink to the bottom of the cell and are withdrawn as the waste or tailings.
- the remaining 15% or less may be fed in stages to the various cells in the rougher" flotation circuit.
- the temperature of the water added to the ore, or of the resulting pulp, is of no importance pulp is eliminated or reduced to a very small percentage of that employed in the prior process.
- EXAMPLE A Two volumes of water and one volume of talloel and a quantity of ethylene glycol oleate amounting to /2%- of the weight of the talloel are passed heretcfereazsedlw through a colloid mill or some other type of high speed mixer thereby producing a stable emulsion or dispersion of the talloel in water.
- quantity of ethylene glycol oleate serves as a stabilizing agent for the dispersion.
- the stable dispersion of talloel so prepared maybe proportioned to the grinding circuit, cells, etc., by means of any of the conventional reagent feeders well known to the art.
- a good dispersion of talloel in water can also be prepared by simply agitating the proper quantity of talloel, water and emulsifying agent in an open tank with a mechanical stirrer or a steam J'et.
- Another modification of this procedure is to add the necessary amount of ethylene glycol oleate to the talloel, the two being miscible in all proportions.
- the mixture of talloel and emulsifying agent are simply proportioned out in conventional manner, mixed with a quantity of water, passed through an emulsifying machine and the resulting emulsion conducted to the grinding circuit, cells, etc.
- This procedure is a very simple one since the quantity of water used in making up the emulsion is not critical as it is in the previous case when the reagent is proportioned after emulsification.
- ethylene glycol oleate In place of ethylene glycol oleate, other neutral, organic, oil-soluble emulsifying agents may be used; for example: diglycol stearate, glycerol monostearate, diglycol laurate, glycerol monorecinoleate, propylene glycol oleate, propylene glycol stearate, diglycol palmita-te, propylene glycol monoricinoleate.
- EXAMPLE B A quantity of triethanol amine amounting to 5% of that which would be necessary theoretically to saponify the acid content of talloel, is dis-' solved in a portion of talloel, the two being miscible in all proportions.
- the mixture of talloel and triethanol amine is proportioned out, mixed with water and emulsified, using the same procedure as in Example A.
- EXAMPLE C i A quantity of sodium hydroxide, or other water soluble inorganic basic substances capable of forming a water soluble soap with the talloel acids, amounting to 4% of that which will theoretically saponify the acid content of the talloel, is dissolved in a portion of water.
- the water containing the caustic agent and the talloel are proportioned out in the proper ratio and passed through a high speed mixer or colloid. mill, thereby producing a stable emulsion having an average The small particle size in the neighborhood of 1 micron.
- the small amount of soap formed by the interaction of the caustic agent with the talloel acids acts as the emulsifying and stabilizing agent.
- agents of this type includes the following: aliphatic sulphonlc acids or their sodium salts, sulphate esters of fatty alcohols of their sodium salts, etc.
- a neutralhydrocarbon oil such as gas oil, crude oil or fuel oil
- the oil is simply mixed with the talloel in the proper proportion before emulsifica'tion.
- the presence of the neutral oil in no way -affects the particle size or stability of the emulsions.
- EXAMPLE #1 An emulsion of crude talloel in water was pre pared by passing through a colloid mill one volume of talloel and two volumes of water, in which suflicient sodium hydroxide had been dissolved to saponify 2% of the total acid content of the talloel.
- the resulting stable dispersion had an average particle size of about 1 micron.
- the prepared pulp which had a pH of 7.1, was
- first concentrate, or rougher concentrate was then subjected to a second flotation after the addition of a-small amount of an acidic cleaning agent.
- an acidic cleaning agent such as carbonic acid, sulphuric acid I and the like.
- the amount of cleaning agent used is generally in the neighborhood of per ton. We have found, however, that in mill practice the use of cleaning agents can be omitted entirely.
- the pulp was made alkaline with 2.0# of sodium hydroxide, and, after mixing the caustic soda thoroughly with the pulp, the equivalent of 5# per ton of gas oil was added. Finally, crude talloel in an amount equivalent to 10# per ton was added to and thoroughly incorporated into the pulp.
- the treated pulp which has a pH of 9.3 was then subjected to flotation in the same cell used in the above example of my invention. The result was the formation of a voluminous, tenacious wild froth that could not be controlled and which only diminished after practically all the ore charge had been carried over into the concentrate; in other words, no economic separation was affected.
- EXAMPLE #2 An emulsion of crudetalloel in water was prepared by dissolving in a volume of talloel suflicient triethanol amine to saponify 3% of the acid content of the talloel. The combination of talloel and triethanol amine was mixed with two volumes of water and passed through a high speed mixer, whereby a stable emulsion was formed. The average particle size of the emulsion was about .5-.'75 microns.
- EXAMPLE #3 An emulsion of crude talloel in water was prepared by passing through a colloid machine one volume of talloel and two volumes of water in which was dissolved .I%, based upon the weight of talloel used, of a hydrocarbon sulphonate. The average particle size of the resulting stable emulsion was found to average less than 1 micron in diameter. A volume of emulsion equivalent to 10: per ton of feed was added to. a charge of low grade manganese ore in a rod mill, together with sufficient water to give the ground pump a solids content of 25%. The ore was then ground to such a fineness that 85% of the resulting pulp passed through a 100 mesh screen.
- the prepared pulp which had a pH of 6.95, was placed in a mechanical, sub-aeration type flotation machine. An amount of gas oil equivalent to 5# per ton of ore feed was added in stages throughout the flotation. A froth containing the valuable minerals was taken off at the top of the cell, and the worthless gangue or tailings. was removed from the bottom of the machine.
- EXAMPLE #4 An emulsion of crude talloel in water was pre-- pared by passing through a colloid machine three volumes of water and one volume of talloel in which was dissolved 1% by weight of propylene glycol oleate, an oil-soluble emulsifying agent.
- the stable emulsion formed in this mariner had an average particle size of less than 1 micron.
- a volume of this emulsion equivalent to 8# per ton of feed was added to a charge of low grade manganese ore in a rod mill, together with suflicient water to give the ground pulp a solids content of 35%. The ore was then ground to such a fineness that 85% of the resulting pulp passed through a 100 mesh screen.
- the prepared pulp which was found to have a pH of 7.1, was placed in a flotation machine of the same type used in the previous examples, and the flotation was carried out in the same manner as 'described in Example #1. In this example, however, the equivalent of 5#/ton of gas oil was fed to the cell during the rougher operation.
- the results obtained in this example are set forth in Table IV.
- Ores of various types can be successfully treated regardless of the physical characteristics of the minerals, without the necessity of sizing or classifying the pulp to remove the undesirable slime material.
- By operating at a pH less than 7.4 much of the undesirable frothing which is characteristic of talloel reagents is eliminated; thus I am able to produce a product of commercial grade with the minimum of cleaning operations.
- Any type of talloel may be used, the crude material being just as effective as the purified products per unit of acid content.
- the cost of concentrating a given ore is reduced when my reagent is used due to the facts that no losses are incurred by a selective sizing operation, the cheapest grades of talloel may be used, little or no caustic or other alkalizing or saponifying agent need be used, etc.
- My reagent is easy to prepare, is more stable and more easily proportioned in all types of equipment under more diversified temperature conditions.
- the use of an auxiliary hydrocarbon is eliminated or reduced to a minimum.
- the process of concentrating oxidized manganese ore which comprises grinding the ore, contacting the ore during the grinding operation with water and an aqueous dispersion of crude talloel having an average particle size not substantially in excess of 1 micron, thereby producing watery pulp having a pH of not more than 7.4 and a solids content of about 20 to 35%, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth.
- the process of concentrating oxidized manganese ore which comprises subjecting to a flotation operation finely-ground watery pulp containing the ore in intimate admixture with an aqueous dispersion of crude talloel, said pulp having a pH of not more than 7.4 and a solids content of about 20 to 35 per cent.
- the process of concentrating oxidized manganese ore which comprises forming an aqueous dispersion of crude talloel, grinding the ore, combining the ore with said dispersion during the grinding operation and producing watery pulp having a pH of not more than 7.4 and a solids content of about 20-35 per cent, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth.
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Description
Patented Oct. 14, 1941 a A i UNITED'STATES PATENTgOFFlCE 2,259,420 t FLOT'ATIONPROCESSFOR oxmrznn MANGANESE one a Robert C. Hills, Port Sulphur, La., assignor to Freeport Sulphur Company, New York, N. Y., a corporation of Delaware No Drawing. Application February 1, 1939, Serial No. 254,007
10 Claims. (Cl. 209166) The present invention relates to flotation procfrom the gangue in order that a flotation separaesses and flotation reagents for use in the seption may be effected. The tendency for talloel aration of minerals, with particular reference to soap, or talloel in highly alkaline pulps, to give the concentration of oxidized metallic ores, such 7 avoluminous tenacious froth is even more serious I as the oxidized ores of manganese. 1 when both the ore and gangue materials have It is an object'of my invention to provide a pronounced sliming characteristics. The low flotation process which gives improved recovergrade manganese ores of Eastern Cuba are a ies and higher grade concentrates, at lower costs notable example of this type of ore. Sliming of operation, in the flotation of oxidized metallic ores are especially hard to concentrate with talores. loel soap, or by the addition of talloel to highly Another object of my invention is to provide 4 alkaline pulps, because the slime, much of which flotation reagents which are cheaper and more may extend into the true colloidal range, tends easily prepared than any now known in the art. to stabilize the froth. This tendency of slime Another object of the invention is to provide to stabilizethe froth is especially marked in a flotation process which gives efficient recovl5 pulps of high alkalinity. Stabilization of the cries of valuable ore concentrates in the treatfroth lessens the chance for coarse gangue' par mentof highly refractory oxidized metallic'ores, ticles to fall back into the pulp; therefore, there such as the oxidized ores of manganese that exis a lowering of the grade of the concentrate due hibit pronounced sliming characteristics when to mechanical entrainment of gangue. Moreground to a size permitting separation of the ore over, since the forces of surface tension are minerals from the gangue. greater than the forces of gravity on extremely Further objects and advantages of the infine particles, all of the slime in the froth goes vention will become apparent from the following over with the ore minerals particles" and endescription. trained coarse gangue particles. The mechani- It has heretofore been proposed to carry out cal carry-over of both coarse gangue andslime the concentration of oxidized alkaline earth ores produces a low grade concentrate which is dif by flotation in the presence of a flotation reagent flcult, and in many cases, impossible to clean consisting of a soap or highly alkaline dispersion to a grade that is marketable. made from the mixture of fatty and resin acids, I rd m minimize diflicultie heretofore known as talloel, that is recov ed s a bycountered in the flotation of sliming ores, it has Product i e manufacture of Paper and P p been necessary to classify the ore pulps into from resinous Woods by the Sulfate selected sizes before the flotation treatment; in p other words, pulps are used which have been sub- According to this prior practice, purified taljected to some type f deesnmmg process, Such loel is either saponified with sodium hydroxide 3 as by mechanical or hydraulic classification or or other caustic agent and added to a by simple decantation of fine material. Classiwatery pulp of the or the tanoel is added to flcationto any selected size range before flotation an ore pulp which has been made alkaline w naturally increases the loss of valuable minerals a suitable caustic agent, thereby forming the in the fine sizes and when both the ore and Soap Sit? the amount of caustic beingreg' 40 gangue minera1s have a tendency to slime the mated to maintain high degree of alkalinity in losses make such treatment economically im- 'the pulp 'after-themddition ot- .the talloel. practical A characteristic of these known proc'edures is H \u a the production of a voluminous froth which is It has also been proposed to use a neutral extremely difficult to handle in the actual flotation process. The frothing characteristic of tal- 22 tame! 32 in a g n f loel soaps, or talloel in alkaline solutions, has ime excesswe m g g e posed serious limitations on the application of P and t i a 58186 talloel as a flotationagent for ores of diverse Y Slzed flotatlon feed t h1s expedleft has met with some success, but with unclassified pulps,
qualities. w
This difiiculty is especially marked when treatespeclany wlth 0118s contammg Shmy ganguemg ores containing a gangue material that has slimy ore minerals, or both, the use of the auxilbeen reduced to a fine state of division. or slime" iary hydrocalbon 0115 has been of "31W; as known in the art, in the grinding operations when employed to any appreciable advantage, :1 which are necessary to free the ore materials illlimilty Of 011 1 equired.
drocarbon oil, such as gas 'oil'pr fue'l oihalong more than pH 7.4. Thus I have found it possible to obtain efflcient flotation and concentration of valuable ore minerals, giving improved recoveries and a higher grade of concentrates, and
when my reagent is used due to the fact that the reagent is liquid and can be readily proportioned or handled at any temperature encountered in ordinary practice.
In those cases where it is desirable to use a 7 neutral hydrocarbon oil, such as gas oil, fuel oil and the like, the oil may be emulsified with the talloel, added to the grind separately, or fed in stages to the various flotation cells. I have found that especially good results are obtained where at least a part of the neutral hydrocarbon oil is fed these results may be obtained when treating pulps of diverse qualities without encountering the restrictive and costly requirements involved in the use of the known processes.
Moreover, I have found that the flotation process can be carried out successfully, in many cases,
' without requiring an auxiliary hydrocarbon oil, and in those cases where it is desirable to usesuch an oil the amount employed is only a small proportion-of that used according to prior processes employing talloel.
Another important feature of my improved process is that any type of talloel can be used effectively, the gravity, acid number, iodine num ber, etc, beihg relatively unimportant. In other words, I have found that it is not necessary to use a purified talloel, "the material produced by simple acidulation'of. crude black liquor soap being entirely suitable. The lignins, etc., present in this material simply act as harmless diluents.
Another important feature of my improved process and reagent is that they minimize the frothing characteristics of talloel, thus eliminating to a great degree the mechanical carry-over of coarse gangue and slime. ThusI am able to produce a product of suitable grade with a minimum of. cleaning operations, .fromthe most refractory ores, without the necessity of selectively sizing the flotation feed by classification, desliming or other mechanical treatment.
According to the present invention, oxidized metallic ores, such as oxidized ores of manganese, are subject to the usual coarse crushing operations to produce a size range suitable for further reduction in a rod or ball mill or other fine grinding mill. A dispersion of talloel in water, constituting the flotation reagent, is prepared by mixing; the talloel and water in the presence of a small amount of emulsifying agent, which may be an added organic, neutral, oil-soluble'or water-soluble material, or a material produced in situ by the addition of a small amount of an organic talloel-soluble base or an inorganic watersoluble base, depending upon the procedure selected for preparing the dispersion. The coarsely crushed ore is fed to a rod or ball mill operating in closed circuit with a mechanical classifier for returning insufficiently ground material to the mill. At the grinding mill water and the emulsified talloel reagent are added to theorem the -properf.preportions. Ihavefound that best results are secured when the water content is ad-- justed to such an amount that the solids represent from about 20 to 35% of the total mass of the pulp. I have further found that best results gives good results. The ore minerals particles are levitated to the surface of the pulp by attachment to the air bubbles introduced into the pulp. The ore minerals become preferentially attached to the air bubbles due to the fact that the emulsified talloel reagent selectively .coats the surfaces of the ore minerals with a water repellent, nonpolar film which has a greater affinity for the'air than for water, the gangue minerals being entirely unaffected by the treatment. The-mineral laden bubbles, or concentrate, is collected as a froth on the surface of the pulp; the gangue minerals, being unaffected by the presence of the emulsified talloel reagent, remain wetted by the water of the pulp, sink to the bottom of the cell and are withdrawn as the waste or tailings.
There are, of course, several cell combinations which may be used to effect the separation of ore minerals and gangue, as will be appreciated by persons skilled in the art; The usual practice is to treat the pulp in one or more cells to produce a tailing product and a concentrate contaminated with some low grade material. The concentrate from the first cell or group of cells is conducted to a second cell or group of cells where another separation is made, thus improving the grade of the concentrate. The tailings from the second flotation separation are generally recirculated .through the grinding system to free any chatted efficiency of this contact could be increased only by complete solution of the talloel, since the reagents here involved have an average particle size of about 1 micron or less. In the practice of the present process, the cost of treating a given amount of ore is reduced due to the facts that the equipment necessary for the production of soap is eliminamdand-taeeaus' 'cfor'sa'ponification or for producing an alkaline ing mill; by substantially, I mean 85% or more.
The remaining 15% or less may be fed in stages to the various cells in the rougher" flotation circuit. The temperature of the water added to the ore, or of the resulting pulp, is of no importance pulp is eliminated or reduced to a very small percentage of that employed in the prior process.
In order to indicate completely suitable manners of practicing the present invention, the following examples of the preparation of my improved flotation reagent are given by way of iilustration.
EXAMPLE A Two volumes of water and one volume of talloel and a quantity of ethylene glycol oleate amounting to /2%- of the weight of the talloel are passed heretcfereazsedlw through a colloid mill or some other type of high speed mixer thereby producing a stable emulsion or dispersion of the talloel in water. quantity of ethylene glycol oleate serves as a stabilizing agent for the dispersion. Measurements of the particle size, after allowing the dispersion to stand for several hours, show the average diameter of the talloel globules to be about 1 micron. The stable dispersion of talloel so prepared maybe proportioned to the grinding circuit, cells, etc., by means of any of the conventional reagent feeders well known to the art.
A good dispersion of talloel in water can also be prepared by simply agitating the proper quantity of talloel, water and emulsifying agent in an open tank with a mechanical stirrer or a steam J'et.
Another modification of this procedure is to add the necessary amount of ethylene glycol oleate to the talloel, the two being miscible in all proportions. The mixture of talloel and emulsifying agent are simply proportioned out in conventional manner, mixed with a quantity of water, passed through an emulsifying machine and the resulting emulsion conducted to the grinding circuit, cells, etc. This procedure is a very simple one since the quantity of water used in making up the emulsion is not critical as it is in the previous case when the reagent is proportioned after emulsification.
In place of ethylene glycol oleate, other neutral, organic, oil-soluble emulsifying agents may be used; for example: diglycol stearate, glycerol monostearate, diglycol laurate, glycerol monorecinoleate, propylene glycol oleate, propylene glycol stearate, diglycol palmita-te, propylene glycol monoricinoleate.
I have found that .25 to 2% of the emulsifying agent, in relation to the mass of talloel, is ample for the production of a suitable dispersion. The amount of emulsifying agent to be used, however, is not at all critical.
EXAMPLE B A quantity of triethanol amine amounting to 5% of that which would be necessary theoretically to saponify the acid content of talloel, is dis-' solved in a portion of talloel, the two being miscible in all proportions. The mixture of talloel and triethanol amine is proportioned out, mixed with water and emulsified, using the same procedure as in Example A. The triethanol amine,
EXAMPLE C i A quantity of sodium hydroxide, or other water soluble inorganic basic substances capable of forming a water soluble soap with the talloel acids, amounting to 4% of that which will theoretically saponify the acid content of the talloel, is dissolved in a portion of water. The water containing the caustic agent and the talloel are proportioned out in the proper ratio and passed through a high speed mixer or colloid. mill, thereby producing a stable emulsion having an average The small particle size in the neighborhood of 1 micron. The small amount of soap formed by the interaction of the caustic agent with the talloel acids acts as the emulsifying and stabilizing agent.
- droxide.
EXAMPLE D "agents of this type includes the following: aliphatic sulphonlc acids or their sodium salts, sulphate esters of fatty alcohols of their sodium salts, etc.
Should it be desired to use a neutralhydrocarbon oil such as gas oil, crude oil or fuel oil as a part of the emulsified reagent, the oil is simply mixed with the talloel in the proper proportion before emulsifica'tion. The presence of the neutral oil in no way -affects the particle size or stability of the emulsions.
The advantages and utility of the present invention are clearly indicated :by the results obtained in the practice of my process on low grade manganese ores of Eastern Cuba, which represent one of the most refractory types of oxidized metallic ores. These ores contain the various oxides of manganese together with impurities such as iron oxides, silica; calcium carbonate, hydrated silicates and the like. The ore minerals as well as the gangue minerals have pronounced sliming characteristics; for example, a grind which is sufiicient to liberate the ore minerals will reduce the ore to such a degree of fineness that as much as 20 to 25% of a normal deflecculated pulp will be found remaining in suspension after settling for a period of two hours in a 1000 cc. graduate: The suspended material contains slimed ore materials as well as slimed gangue, as demonstrated by the following analysis.
Per cent Mn Heads 19.2 Material remaining in suspension after 4 hours 17.1 ,Mat'erial settled out after 4 hours 20.0
capable of efiecting an eflicient separation be tween ore and gangue particles in all degrees of fineness.
The following examples are given to illustrate the practice of my process in the treatment of low grade manganese ores of the type mentioned above.
EXAMPLE #1 An emulsion of crude talloel in water was pre pared by passing through a colloid mill one volume of talloel and two volumes of water, in which suflicient sodium hydroxide had been dissolved to saponify 2% of the total acid content of the talloel. The resulting stable dispersion had an average particle size of about 1 micron. An amount of this emulsion equivalent to 10# of talloel per ton of feed was added to an ore charge in a rod mill, together with gas oil amounting to 5:: per ton of ore and's'ufficient water to give a pulp having a solid content of 25%; The ore was then ground tosuch a fineness that 85% of the resulting pulp passed through a 100 mesh screen.
The prepared pulp, which had a pH of 7.1, was
placed in a mechanical, sub-aeration type flotation machine. A froth containing the valuable minerals was taken ofi at the top of the machine, and the worthless gangue or tailings was removed from the bottom of the machine. The
first concentrate, or rougher concentrate, was then subjected to a second flotation after the addition of a-small amount of an acidic cleaning agent. such as carbonic acid, sulphuric acid I and the like.- The amount of cleaning agent used is generally in the neighborhood of per ton. We have found, however, that in mill practice the use of cleaning agents can be omitted entirely.
The results of this example are shown in Table I. Table I Wt. t Mn Dist. Recovery Percent Percent Percent Percent Feed l 100. 2o. 5 100.0 Final tailings 35. 3 7. 4 18. 3 Cleaner concentrate-.. 22.4 45.0 32.4 81 7 Cleaner tails 25. l 26. 4 49. 3
/ solids. The pulp was made alkaline with 2.0# of sodium hydroxide, and, after mixing the caustic soda thoroughly with the pulp, the equivalent of 5# per ton of gas oil was added. Finally, crude talloel in an amount equivalent to 10# per ton was added to and thoroughly incorporated into the pulp. The treated pulp, which has a pH of 9.3 was then subjected to flotation in the same cell used in the above example of my invention. The result was the formation of a voluminous, tenacious wild froth that could not be controlled and which only diminished after practically all the ore charge had been carried over into the concentrate; in other words, no economic separation was affected.
EXAMPLE #2 An emulsion of crudetalloel in water was prepared by dissolving in a volume of talloel suflicient triethanol amine to saponify 3% of the acid content of the talloel. The combination of talloel and triethanol amine was mixed with two volumes of water and passed through a high speed mixer, whereby a stable emulsion was formed. The average particle size of the emulsion was about .5-.'75 microns. A volume of this emulsion equivalent to 10# of talloel per ton of feed was added to a charge of low grade manganese ore in a rod mill, together with suflicient water to give a pulp having a solids content of about No auxiliary neutral hydrocarbon oil was used in this test. The ore charge was ground. and treated in accordance with the method described in Example #1. The pH of the prepared pulp was found. to be 7.05.
0 The results of this example are indicated in Table II.
Table II 25 Wt. Mn Dist. Recovery Perccnl Per Fecdl 100 0 After sintering, the cleaner concentrate produced a product running over 50% manganese, an exceptionally high grade product suitable for the production of term-manganese.
EXAMPLE #3 An emulsion of crude talloel in water was prepared by passing through a colloid machine one volume of talloel and two volumes of water in which was dissolved .I%, based upon the weight of talloel used, of a hydrocarbon sulphonate. The average particle size of the resulting stable emulsion was found to average less than 1 micron in diameter. A volume of emulsion equivalent to 10: per ton of feed was added to. a charge of low grade manganese ore in a rod mill, together with sufficient water to give the ground pump a solids content of 25%. The ore was then ground to such a fineness that 85% of the resulting pulp passed through a 100 mesh screen. The prepared pulp, which had a pH of 6.95, was placed in a mechanical, sub-aeration type flotation machine. An amount of gas oil equivalent to 5# per ton of ore feed was added in stages throughout the flotation. A froth containing the valuable minerals was taken off at the top of the cell, and the worthless gangue or tailings. was removed from the bottom of the machine.
The results of thistest are indicated in Table III.
Table I 11 Wt. Mn Dist. Recover l y Percent Percent Percent Percent Feed s 100. 0 31. 5 100. U Final tailings .l 37.5 7.7 9.5 Concentrate 02. 5 44. l 90. 5 90. 5
In,this case it was not necessary to clean the first concentrate in order to produce a product which, on sintering, would have a grade in the neighborhood of 53% or, in other words, a grade.
suitable for the production of ferro-manganese.
awi .i
EXAMPLE #4 An emulsion of crude talloel in water was pre-- pared by passing through a colloid machine three volumes of water and one volume of talloel in which was dissolved 1% by weight of propylene glycol oleate, an oil-soluble emulsifying agent. The stable emulsion formed in this mariner had an average particle size of less than 1 micron. A volume of this emulsion equivalent to 8# per ton of feed was added to a charge of low grade manganese ore in a rod mill, together with suflicient water to give the ground pulp a solids content of 35%. The ore was then ground to such a fineness that 85% of the resulting pulp passed through a 100 mesh screen. The prepared pulp, which was found to have a pH of 7.1, was placed in a flotation machine of the same type used in the previous examples, and the flotation was carried out in the same manner as 'described in Example #1. In this example, however, the equivalent of 5#/ton of gas oil was fed to the cell during the rougher operation. The results obtained in this example are set forth in Table IV.
For purposes of comparing this process with the process of the prior art, a sample of the same ore was ground in a rod mill, to-the same fineness as used in the above example, with sufficient water to produce a pulp containing 70% solids. .To the ground pulp the equivalent of 8#/ton of a crude talloel soap and 5#/ton of gas oil were added and thoroughly incorporated into the pulp. The talloel soap was prepared by carefully saponifying talloel, in the well known manner, with the proper quantity of sodium hydroxide to give a pulp having an alkalinity of about pH 9.1.
in the same cell used in the above example of my invention. The result was the formation of an The treated pulp was then subjected to flotation extremely voluminous, tenacious froth that could not be controlled, and the test had to be discontinued.
The advantages of the present invention may be summarized as follows:
Ores of various types can be successfully treated regardless of the physical characteristics of the minerals, without the necessity of sizing or classifying the pulp to remove the undesirable slime material. By operating at a pH less than 7.4 much of the undesirable frothing which is characteristic of talloel reagents is eliminated; thus I am able to produce a product of commercial grade with the minimum of cleaning operations. Any type of talloel may be used, the crude material being just as effective as the purified products per unit of acid content. By use of my dispersed reagent intimate contact between ore minerals and reagent is assured, thereby increasing the efliciency of the flotation process. The cost of concentrating a given ore is reduced when my reagent is used due to the facts that no losses are incurred by a selective sizing operation, the cheapest grades of talloel may be used, little or no caustic or other alkalizing or saponifying agent need be used, etc. My reagent is easy to prepare, is more stable and more easily proportioned in all types of equipment under more diversified temperature conditions. The use of an auxiliary hydrocarbon is eliminated or reduced to a minimum.
It should be understood that the present invention is in no way limited to the specific emulsifying agents or procedural steps givenyvariations may be resorted to, as anyone skilled in the art will readily understand.
I claim: 1 v
1. The process of concentrating oxidized manganese ore which comprises grinding the ore. combining the ore with an aqueous dispersion of talloel and producing watery pulp having a pH of not more than 7.4, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth.
2. The process of concentrating oxidized manganese ore which comprises crushing the ore to condition the same for fine grinding, preparing an aqueous dispersion of crude talloel, grinding the ore, combining the ore during the grinding operation with said dispersion and water to produce watery pulp having a, pH of not more than 7.4, subjecting said pulp to a flotation operation to form a froth containing ore minerals. and collecting said froth.
3. The process of concentrating oxidized manganese ore which comprises grinding the ore, contacting the ore during the grinding operation with water and an aqueous dispersion of crude talloel having an average particle size not substantially in excess of 1 micron, thereby producing watery pulp having a pH of not more than 7.4 and a solids content of about 20 to 35%, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth.
4. The process of concentrating oxidized manganese ore which comprises subjecting to a flotation operation finely-ground watery pulp contain- .ing the ore in intimate admixture with an aqueous dispersion of talloel, said pulp having a pH of not more than 7.4.
5. The process of concentrating oxidized manganese ore which comprises subjecting to a flotation operation finely-ground watery pulp containing the ore in intimate admixture with an aqueous dispersion of crude talloel, said pulp having a pH of not more than 7.4 and a solids content of about 20 to 35 per cent.
6. The process of concentrating oxidized manganese ore which comprises grinding the ore, combining the ore during the grinding operation with an aqueous dispersion of talloel and producing watery pulp having a pH of not more than 7.4, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth. i
7. The process of concentrating oxidized manganese ore which comprises forming an aqueous dispersion of crude talloel, grinding the ore, combining the ore with said dispersion during the grinding operation and producing watery pulp having a pH of not more than 7.4 and a solids content of about 20-35 per cent, subjecting said pulp to a flotation operation to form a froth containing ore minerals, and collecting said froth.
8. The process of concentrating oxidized manganese ore which comprises grinding the ore, combining the ore with water and an aqueous dispersion of talloel in proportions forming watery pulp containing'about 20 to 35 $1 of solids, saidpulp having a, pH of not more than 7.4, contactmg m ore with substantially allot said dis- 10. The process of concentrating oxidized manganese -ore which comprises combining the ore in ground form with an aqueous dispersion of talloel present for the most part in its acid or unneutralized form, forming a watery pulp having a pH value of not more than 7.4,producing .a. froth containing the ore minerals and collecting said froth.
ROBERT c. HILLS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US254007A US2259420A (en) | 1939-02-01 | 1939-02-01 | Flotation process for oxidized manganese ore |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US254007A US2259420A (en) | 1939-02-01 | 1939-02-01 | Flotation process for oxidized manganese ore |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2259420A true US2259420A (en) | 1941-10-14 |
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|---|---|---|---|
| US254007A Expired - Lifetime US2259420A (en) | 1939-02-01 | 1939-02-01 | Flotation process for oxidized manganese ore |
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| US (1) | US2259420A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2636604A (en) * | 1949-06-17 | 1953-04-28 | Bethlehem Steel Corp | Flotation of pyrites from a pyrite ore pulp |
| US2657147A (en) * | 1948-11-23 | 1953-10-27 | Edward A Van Valkenburgh | Composition for vulcanizing rubber |
| US2698088A (en) * | 1952-03-11 | 1954-12-28 | Pryor Edmund James | Separation of minerals by froth flotation |
| US2784468A (en) * | 1952-03-11 | 1957-03-12 | American Cyanamid Co | Clarification of black foundry waste waters |
| US3151062A (en) * | 1961-02-01 | 1964-09-29 | Minerals & Chem Philipp Corp | Method for the froth flotation of slimed minerals and ores |
| US3827556A (en) * | 1972-11-06 | 1974-08-06 | Engelhard Min & Chem | Purification of kaolin clay by froth flotation |
| US3837489A (en) * | 1972-11-24 | 1974-09-24 | Nalco Chemical Co | Molybdenum disulfide flotation antifoam |
| US4211644A (en) * | 1976-11-26 | 1980-07-08 | Pennwalt Corporation | Froth flotation process and collector composition |
| US4220525A (en) * | 1978-12-28 | 1980-09-02 | Vojislav Petrovich | Beneficiation of metallic ores by froth flotation using polyhydroxy amine depressants |
| US4274866A (en) * | 1978-07-24 | 1981-06-23 | Kennecott Copper Corporation | Flotation and sintering of synthetic manganese carbonate |
| US4337149A (en) * | 1981-05-11 | 1982-06-29 | Sherex Chemical Company, Inc. | Promoters for use in the anionic circuit of froth flotation of mineral ores |
| EP2017009A1 (en) * | 2007-07-20 | 2009-01-21 | Clariant (Brazil) S.A. | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
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- 1939-02-01 US US254007A patent/US2259420A/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2657147A (en) * | 1948-11-23 | 1953-10-27 | Edward A Van Valkenburgh | Composition for vulcanizing rubber |
| US2636604A (en) * | 1949-06-17 | 1953-04-28 | Bethlehem Steel Corp | Flotation of pyrites from a pyrite ore pulp |
| US2698088A (en) * | 1952-03-11 | 1954-12-28 | Pryor Edmund James | Separation of minerals by froth flotation |
| US2784468A (en) * | 1952-03-11 | 1957-03-12 | American Cyanamid Co | Clarification of black foundry waste waters |
| US3151062A (en) * | 1961-02-01 | 1964-09-29 | Minerals & Chem Philipp Corp | Method for the froth flotation of slimed minerals and ores |
| US3827556A (en) * | 1972-11-06 | 1974-08-06 | Engelhard Min & Chem | Purification of kaolin clay by froth flotation |
| US3837489A (en) * | 1972-11-24 | 1974-09-24 | Nalco Chemical Co | Molybdenum disulfide flotation antifoam |
| US4211644A (en) * | 1976-11-26 | 1980-07-08 | Pennwalt Corporation | Froth flotation process and collector composition |
| US4274866A (en) * | 1978-07-24 | 1981-06-23 | Kennecott Copper Corporation | Flotation and sintering of synthetic manganese carbonate |
| US4220525A (en) * | 1978-12-28 | 1980-09-02 | Vojislav Petrovich | Beneficiation of metallic ores by froth flotation using polyhydroxy amine depressants |
| US4337149A (en) * | 1981-05-11 | 1982-06-29 | Sherex Chemical Company, Inc. | Promoters for use in the anionic circuit of froth flotation of mineral ores |
| WO2009077015A1 (en) * | 2007-07-20 | 2009-06-25 | Clariant (Brazil) S.A. | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
| EP2017009A1 (en) * | 2007-07-20 | 2009-01-21 | Clariant (Brazil) S.A. | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
| CN101795776A (en) * | 2007-07-20 | 2010-08-04 | 科莱恩(巴西)私人控股公司 | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
| US20100213105A1 (en) * | 2007-07-20 | 2010-08-26 | Clariant (Brazil) S.A. | Reverse Iron Ore Flotation By Collectors In Aqueous Nanoemulsion |
| US8784678B2 (en) | 2007-07-20 | 2014-07-22 | Clariant S.A. | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
| US9403174B2 (en) | 2007-07-20 | 2016-08-02 | Clariant S.A. | Reverse iron ore flotation by collectors in aqueous nanoemulsion |
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| WO2018114741A1 (en) | 2016-12-23 | 2018-06-28 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
| AU2017381628B2 (en) * | 2016-12-23 | 2020-01-02 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
| RU2722484C1 (en) * | 2016-12-23 | 2020-06-01 | Акцо Нобель Кемикалз Интернэшнл Б.В. | Phosphate ore processing method |
| US20200222914A1 (en) * | 2016-12-23 | 2020-07-16 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
| CN110087776B (en) * | 2016-12-23 | 2020-07-17 | 阿克苏诺贝尔化学品国际有限公司 | Method for processing phosphate ore |
| US11607696B2 (en) * | 2016-12-23 | 2023-03-21 | Nouryon Chemicals International B.V. | Process to treat phosphate ores |
| SE1951053A1 (en) * | 2019-09-18 | 2021-03-19 | Pavlos Christakopoulos | A collector for froth flotation, a method for producing the collector and the use thereof |
| SE544632C2 (en) * | 2019-09-18 | 2022-09-27 | Pavlos Christakopoulos | A collector for froth flotation, a method for producing the collector and the use thereof |
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