US3380666A - Process for obtaining potash values from potash ore - Google Patents
Process for obtaining potash values from potash ore Download PDFInfo
- Publication number
- US3380666A US3380666A US478443A US47844365A US3380666A US 3380666 A US3380666 A US 3380666A US 478443 A US478443 A US 478443A US 47844365 A US47844365 A US 47844365A US 3380666 A US3380666 A US 3380666A
- Authority
- US
- United States
- Prior art keywords
- potash
- ore
- fraction
- flotation
- finer
- 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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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 title description 22
- 229940072033 potash Drugs 0.000 title description 22
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 title description 22
- 235000015320 potassium carbonate Nutrition 0.000 title description 22
- 238000000034 method Methods 0.000 title description 18
- 238000005188 flotation Methods 0.000 description 25
- 239000003153 chemical reaction reagent Substances 0.000 description 24
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 16
- 150000001412 amines Chemical class 0.000 description 15
- 239000012141 concentrate Substances 0.000 description 15
- 229910052700 potassium Inorganic materials 0.000 description 11
- 238000009291 froth flotation Methods 0.000 description 8
- 239000001103 potassium chloride Substances 0.000 description 8
- 235000011164 potassium chloride Nutrition 0.000 description 8
- 238000011084 recovery Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- 238000012216 screening Methods 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- -1 aliphatic amines Chemical class 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 235000007575 Calluna vulgaris Nutrition 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- 101100130497 Drosophila melanogaster Mical gene Proteins 0.000 description 1
- 229910020549 KCl—NaCl Inorganic materials 0.000 description 1
- 101100345589 Mus musculus Mical1 gene Proteins 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 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
- B03D1/06—Froth-flotation processes differential
Definitions
- This invention relates to a process for Obtaining desired mineral values from ore by froth flotation and especially to obtaining potash from potash ore.
- Froth flotation of potash from potash ores such as sylvinite, which is predominantly potassium chloride and sodium chloride, is generally accomplished by crushing the ore to the point of KCl-NaCl liberation, treating the ore to remove insoluble clays, reagentizing the treated ore with flotation reagents which have an aflinity for potash, and finally separating the KCl from the NaCl in a conventional rougher-cleaner flotation circuit.
- the coarse potash particles generally in the +20 Tyler mesh size range, are far more difficult to float than are the finer particles. Therefore, in order to obtain an acceptable process recovery, it has been found to be necessary to add excessive amounts of flotation reagents to the ore resulting in waste and unenconomical practice.
- Various methods of overcoming this have been suggested, the most successful of which is separation of the coarse and fine fractions of the ore and addition of all the reagent to the coarse ore fraction. The separate fractions are then recombined and introduced to a rougher flotation cell where the KCl is floated and the salt is discarded to Waste.
- the flotation product (concentrate) from the rougher circuit is then refloated in a cleaner flotation circuit designed to produce a concentrate of an acceptable grade and an underflow stream called middlings which contains too much KCl value to be discarded 'as waste from the rougher flotation system.
- middlings which contains too much KCl value to be discarded 'as waste from the rougher flotation system.
- the production of the middlings stream in the cleaner flotation introduces metallurgical problems for receovery of the KCl values in this fraction. It is the practice to screen the middlings and to add the coarse or oversize directly to the concentrate. The fines are then returned to the rougher flotation *circuit.
- the present invention provides a much simpler process for recovering potash from potash ore.
- the ore is comminuted to provide a coarser and a finer fraction which are sized and separated, such as by screening or classifying, and both fractions are separately reagentized with the flotation collector reagents.
- the finer fraction is submitted to a rougher flotation circuit to give a potash concentrate mixed with the collector reagent as a float product which is then combined with the coarse fraction, and the combined stream is then introduced to another rougher flotation circuit.
- the collector reagent in the finer flotation fraction is thus added to the reagent on the coarse fraction and, in effect, extends the beneficial effects of the reagent on the coarse fraction.
- the flotation action of the finer potash helps flotation of the coarser particles and results in a potash concentrate which does not require the conventional cleaner flotation atent 3,38,556 Patented Apr. 30, 1968 step. Also of importance is the fact that a middlings fraction, which is normally associated with a cleaner flotation step, is therefore not formed and this eliminates the requirement of midd'lings fraction treatment steps, such as screening and recycling.
- the present invention provides an improved process which is much simpler and, as a result, more econo'mical than conventional procedures heretofore used.
- the ore for the flotation procedure In preparing the ore for the flotation procedure, it is comminuted, such as by use of conventional ore-crushing equipment, to a particle size preferably in the range of about -8 to '10 mesh.
- the comminuted ore is then pulped by slurrying it in a saturated brine composed of the soluble constituents of the ore. If the ore contains clay contaminants, it is preferred to deslime using conventional procedures such as by screening the slurry through, for example, a or ZOO-mesh screen to remove the clay and fines.
- the deslimed :feed is then split into coarser and finer fractions such as by screening through a screen or classifier.
- the mesh size at which the splitting takes place is not critical, it only being important that the ore is split into two fractions, one of which is coarser than the other.
- fractions are reagentized separately and submitted to froth flotation circuits as described above.
- Conventional flotation temperatures such as in the range of from about 15 to about 35 C., are employed.
- a linding agent such as starch can be added to the liner portion prior to flotation to act as a depressant for the control of slimes.
- the coarser and finer fractions are reagentized separately with the conventional amine flotation reagents Well known to those skilled in the art.
- the saturated or unsaturated long-chain aliphatic amines can be used as collector reagents.
- Typical amines suitable as reagents are those having at least eight carbon atoms per molecule, such as n-octadecyl amine, n-ootadecenyl amine, n-nonylamine, n-decylamine, preferably as the water-soluble salts thereof such as the acetates, and the like.
- the amine collector reagents may be employed either individually or as a mixture containing more than one amine.
- the amine collector reagent may be employed in the form of an aqueous solution, emulsion, or solution in an organic solvent.
- the coarser fraction is preferably reagentized with from about 0.2 to about 0.8 pound of the amine reagent per ton of ore.
- greater or lesser amounts of reagents can be used if desired, but the above amounts are presently preferred.
- auxiliary reagents such as alkylnaphthalenes, the chloro and hydrogenated derivatives thereof, alkylmercaptans, and dialkylsulfides and their aryl derivatives, dialkyl disulfides, dialkyl polysulfides, indane, alkylindanes and polycyclic aromatic compounds, or mixtures thereof, such as described in US. Patents 3,059,774 and 3,149,788, as well as coending US. patent application Ser. No. 397,036 filed Sept. 16, 1964, now Patent No. 3,341,135, by Martin Wilson and assigned to the assignee of the present application.
- EXAMPLE I slurry was deslimed twice on a l-rnesh screen to remove the fines and insoluble matter, and the deslirned ore then wet screened and divided into two fractions; one fraction containing the Tyler mesh particles, and the other fraction containing the 20 Tylor mesh particles.
- the 20 mesh fraction was reagentized with 0.4 pound of starch per ton of ore and 0.13 pound of alkylamine (consisting of tallow amine acetates, of which 75% was saturated) per ton of ore.
- Pine oil (consisting of mixed terpenes) in the amount of 0.05 pound of oil per ton of ore was added to the fraction, which was then floated in a Fag flotation cell.
- the floated fine concentrate was collected for combination with the +20 mesh fraction.
- the +20 mesh fraction was reagentized with 0.32 pound of alkylamine (consisting of the same tallow amine acetates) per ton of ore and with 0.5 pound of Provalent 4A (an aromatic oil containing about 40% polycyclic compounds having at least 3 rings in the molecule, 7% alkylbenzenes and 34% alkylnaphthalenes and alkylindanes) per ton of ore.
- the reagentized coarse raction was then combined with the floated fine concentrate and the resultant combination submitted to a Fag flotation cell.
- the resultant potash concentrate was recovered and analyzed and the tailings were discarded as waste salt.
- the concentrate analyzed 60.63% K 0 (95.8% KCl) and represented 95.88% K 0 recovery.
- the tailings contained 1.41% K 0 and represented 4.22% K 0 recovery.
- Example II The procedure of Example I was repeated.
- the potash concentrate obtained analyzed 60.49% K 0 (95.6% KCl) and represented a 96.86% recovery of K 0.
- the tailings analyzed 108% K 0 and represented a 3.14% K 0 recovery.
- Example III The procedure of Example I was repeated.
- the potash concentrate obtained from the flotation procedure analyzed 60.35% K 0 (95.4% KCl) and represented a recovery of 97.46% K 0.
- the tailings analyzed 0.88% K 0 and represented a 2.54% K 0 recovery.
- the novel process of this invention provides excellent recovery of potash from Sylvinite ore, giving a high-grade product.
- the process eliminates the undesirable middlings product and consequently the required middlings screening and additional processing steps.
- a further advantage is the fact that the coarse and fine tailings are collected separately, which eliminates a possible later waste salt split for retreatinent of the coarse fraction such as by leaching or regrinding.
Landscapes
- Separation Of Solids By Using Liquids Or Pneumatic Power (AREA)
- Disintegrating Or Milling (AREA)
Description
United States ABTRACT OF THE DISCLOSURE Pota'sh is obtained from potash ore by a bene-ficiating procedure in which coarser and finer fractions are reagentized separately and the reagentized finer fraction is subjected to froth flotation to give a concentrate which is combined with the reagentized coarse. The combination is then subjected to another froth flotation procedure to give a highly pure product Without middlings.
This invention relates to a process for Obtaining desired mineral values from ore by froth flotation and especially to obtaining potash from potash ore.
Froth flotation of potash from potash ores such as sylvinite, which is predominantly potassium chloride and sodium chloride, is generally accomplished by crushing the ore to the point of KCl-NaCl liberation, treating the ore to remove insoluble clays, reagentizing the treated ore with flotation reagents which have an aflinity for potash, and finally separating the KCl from the NaCl in a conventional rougher-cleaner flotation circuit.
The coarse potash particles, generally in the +20 Tyler mesh size range, are far more difficult to float than are the finer particles. Therefore, in order to obtain an acceptable process recovery, it has been found to be necessary to add excessive amounts of flotation reagents to the ore resulting in waste and unenconomical practice. Various methods of overcoming this have been suggested, the most successful of which is separation of the coarse and fine fractions of the ore and addition of all the reagent to the coarse ore fraction. The separate fractions are then recombined and introduced to a rougher flotation cell where the KCl is floated and the salt is discarded to Waste. The flotation product (concentrate) from the rougher circuit is then refloated in a cleaner flotation circuit designed to produce a concentrate of an acceptable grade and an underflow stream called middlings which contains too much KCl value to be discarded 'as waste from the rougher flotation system. The production of the middlings stream in the cleaner flotation introduces metallurgical problems for receovery of the KCl values in this fraction. It is the practice to screen the middlings and to add the coarse or oversize directly to the concentrate. The fines are then returned to the rougher flotation *circuit.
The present invention provides a much simpler process for recovering potash from potash ore. According to this invention, the ore is comminuted to provide a coarser and a finer fraction which are sized and separated, such as by screening or classifying, and both fractions are separately reagentized with the flotation collector reagents. The finer fraction is submitted to a rougher flotation circuit to give a potash concentrate mixed with the collector reagent as a float product which is then combined with the coarse fraction, and the combined stream is then introduced to another rougher flotation circuit. The collector reagent in the finer flotation fraction is thus added to the reagent on the coarse fraction and, in effect, extends the beneficial effects of the reagent on the coarse fraction. In addition, the flotation action of the finer potash helps flotation of the coarser particles and results in a potash concentrate which does not require the conventional cleaner flotation atent 3,38,556 Patented Apr. 30, 1968 step. Also of importance is the fact that a middlings fraction, which is normally associated with a cleaner flotation step, is therefore not formed and this eliminates the requirement of midd'lings fraction treatment steps, such as screening and recycling.
Thus, the present invention provides an improved process which is much simpler and, as a result, more econo'mical than conventional procedures heretofore used.
In preparing the ore for the flotation procedure, it is comminuted, such as by use of conventional ore-crushing equipment, to a particle size preferably in the range of about -8 to '10 mesh. The comminuted ore is then pulped by slurrying it in a saturated brine composed of the soluble constituents of the ore. If the ore contains clay contaminants, it is preferred to deslime using conventional procedures such as by screening the slurry through, for example, a or ZOO-mesh screen to remove the clay and fines. The deslimed :feed is then split into coarser and finer fractions such as by screening through a screen or classifier. The mesh size at which the splitting takes place is not critical, it only being important that the ore is split into two fractions, one of which is coarser than the other.
After splitting, the fractions are reagentized separately and submitted to froth flotation circuits as described above. Conventional flotation temperatures, such as in the range of from about 15 to about 35 C., are employed.
If desired, a linding agent such as starch can be added to the liner portion prior to flotation to act as a depressant for the control of slimes.
The coarser and finer fractions are reagentized separately with the conventional amine flotation reagents Well known to those skilled in the art. The saturated or unsaturated long-chain aliphatic amines, generally in the form of their water-soluble addition salts, can be used as collector reagents. Typical amines suitable as reagents are those having at least eight carbon atoms per molecule, such as n-octadecyl amine, n-ootadecenyl amine, n-nonylamine, n-decylamine, preferably as the water-soluble salts thereof such as the acetates, and the like. The amine collector reagents may be employed either individually or as a mixture containing more than one amine. The amine collector reagent may be employed in the form of an aqueous solution, emulsion, or solution in an organic solvent. In the flotation of the finer portion, I prefer to employ from about 0.05 to about 0.5 pound of the amine reagent per ton of ore. The coarser fraction is preferably reagentized with from about 0.2 to about 0.8 pound of the amine reagent per ton of ore. Of course, greater or lesser amounts of reagents can be used if desired, but the above amounts are presently preferred.
Also, to aid in the action of the amine collector reagents, it is preferred to employ auxiliary reagents such as alkylnaphthalenes, the chloro and hydrogenated derivatives thereof, alkylmercaptans, and dialkylsulfides and their aryl derivatives, dialkyl disulfides, dialkyl polysulfides, indane, alkylindanes and polycyclic aromatic compounds, or mixtures thereof, such as described in US. Patents 3,059,774 and 3,149,788, as well as coending US. patent application Ser. No. 397,036 filed Sept. 16, 1964, now Patent No. 3,341,135, by Martin Wilson and assigned to the assignee of the present application.
The following examples are presented for illustration, but the invention is not to be considered limited to the specific examples given.
EXAMPLE I slurry was deslimed twice on a l-rnesh screen to remove the fines and insoluble matter, and the deslirned ore then wet screened and divided into two fractions; one fraction containing the Tyler mesh particles, and the other fraction containing the 20 Tylor mesh particles. The 20 mesh fraction was reagentized with 0.4 pound of starch per ton of ore and 0.13 pound of alkylamine (consisting of tallow amine acetates, of which 75% was saturated) per ton of ore. Pine oil (consisting of mixed terpenes) in the amount of 0.05 pound of oil per ton of ore was added to the fraction, which was then floated in a Fag flotation cell. The floated fine concentrate was collected for combination with the +20 mesh fraction. The +20 mesh fraction was reagentized with 0.32 pound of alkylamine (consisting of the same tallow amine acetates) per ton of ore and with 0.5 pound of Provalent 4A (an aromatic oil containing about 40% polycyclic compounds having at least 3 rings in the molecule, 7% alkylbenzenes and 34% alkylnaphthalenes and alkylindanes) per ton of ore. The reagentized coarse raction Was then combined with the floated fine concentrate and the resultant combination submitted to a Fag flotation cell. The resultant potash concentrate was recovered and analyzed and the tailings were discarded as waste salt. The concentrate analyzed 60.63% K 0 (95.8% KCl) and represented 95.88% K 0 recovery. The tailings contained 1.41% K 0 and represented 4.22% K 0 recovery.
EXAMPLE II The procedure of Example I was repeated. The potash concentrate obtained analyzed 60.49% K 0 (95.6% KCl) and represented a 96.86% recovery of K 0. The tailings analyzed 108% K 0 and represented a 3.14% K 0 recovery.
EXAMPLE III The procedure of Example I was repeated. The potash concentrate obtained from the flotation procedure analyzed 60.35% K 0 (95.4% KCl) and represented a recovery of 97.46% K 0. The tailings analyzed 0.88% K 0 and represented a 2.54% K 0 recovery.
Thus, as can be seen from the above examples, the novel process of this invention provides excellent recovery of potash from Sylvinite ore, giving a high-grade product. The process eliminates the undesirable middlings product and consequently the required middlings screening and additional processing steps. Also, a further advantage is the fact that the coarse and fine tailings are collected separately, which eliminates a possible later waste salt split for retreatinent of the coarse fraction such as by leaching or regrinding.
Various changes and modifications of the invention can be made, and to the extent that such changes incorporate the spirit of this invention they are to be included wtihin the scope of the appended claims.
I claim:
1. In the froth flotation of sylvinite to recover potash values, the steps which include comminuting said sylvinite, to about 8 mesh, pulping said comminuted sylvinite with brine and desliming said pulp, sizing and separating said comminuted and deslimed sylvinite to provide a coarser fraction and a finer fraction, separately reagentizing said finer fraction with amine collector reagent, and submitting the reagentized finer fraction to froth flotation to provide a finer potash concentrate mixed with amine collector reagent, separately reagentizing said coarser fraction with amine collector reagent, combining the reagentized coarser fraction and said finer potash concentrate mixed with amine collector reagent and submitting the resultant combination to froth flotation to provide a clean potash concentrate without formation of a middling fraction.
2. The process according to claim 1 in which said finer fraction is reagentized with from about 0.05 to about 0.5 pound of amine collector reagent per ton of ore and said coarser fraction is reagentized with from about 0.2 to about 0.8 pound of amine collector reagent per ton of ore.
3. The process according to claim 1 in which said finer fraction is about 20 mesh and said coarser fraction is about +20 mesh.
References Cited UNITED STATES PATENTS 2,596,407 5/1952 Jackson 209-166X 2,676,705 4/1954 Duke 209166 3,145,163 8/1964 Dancy 209 12 3,282,418 11/1966 Abernethy 209 12 HARRY B. THORNTON, Primary Examiner.
R. HALPER, Assistant Examiner.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US478443A US3380666A (en) | 1965-08-09 | 1965-08-09 | Process for obtaining potash values from potash ore |
| FR66461A FR1484311A (en) | 1965-08-09 | 1966-06-22 | Process for obtaining potash with suitable yield from potash ore |
| ES0328548A ES328548A1 (en) | 1965-08-09 | 1966-06-30 | Procedure to recover potass by floating. (Machine-translation by Google Translate, not legally binding) |
| OA52541A OA02245A (en) | 1965-08-09 | 1966-07-21 | A process for obtaining potash with a suitable yield from potash ore. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US478443A US3380666A (en) | 1965-08-09 | 1965-08-09 | Process for obtaining potash values from potash ore |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3380666A true US3380666A (en) | 1968-04-30 |
Family
ID=23899957
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US478443A Expired - Lifetime US3380666A (en) | 1965-08-09 | 1965-08-09 | Process for obtaining potash values from potash ore |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US3380666A (en) |
| ES (1) | ES328548A1 (en) |
| OA (1) | OA02245A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3544282A (en) * | 1966-12-06 | 1970-12-01 | Richard Burr | Simplified pretreatment for coarse flotation |
| US3976251A (en) * | 1973-12-19 | 1976-08-24 | Financial Mining - Industrial And Shipping Corporation | Separation of magnesite from its contaminants by reverse flotation |
| US5057208A (en) * | 1984-09-25 | 1991-10-15 | Kali Und Salz Aktiengesellschaft | Method for the production of potassium chloride with K2 O content of more than 55 weight percent |
| US20040144586A1 (en) * | 2003-01-24 | 2004-07-29 | Trott Donald E. | Motorized chariot |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2596407A (en) * | 1949-03-22 | 1952-05-13 | Int Minerals & Chem Corp | Concentration of nonmetallic minerals by flotation |
| US2676705A (en) * | 1951-12-27 | 1954-04-27 | Attapulgus Minerals & Chemical | Concentration of phosphate ores |
| US3145163A (en) * | 1960-10-03 | 1964-08-18 | Int Minerals & Chem Corp | Beneficiation of potash ores |
| US3282418A (en) * | 1963-10-31 | 1966-11-01 | American Metal Climax Inc | Sylvite recovery process |
-
1965
- 1965-08-09 US US478443A patent/US3380666A/en not_active Expired - Lifetime
-
1966
- 1966-06-30 ES ES0328548A patent/ES328548A1/en not_active Expired
- 1966-07-21 OA OA52541A patent/OA02245A/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2596407A (en) * | 1949-03-22 | 1952-05-13 | Int Minerals & Chem Corp | Concentration of nonmetallic minerals by flotation |
| US2676705A (en) * | 1951-12-27 | 1954-04-27 | Attapulgus Minerals & Chemical | Concentration of phosphate ores |
| US3145163A (en) * | 1960-10-03 | 1964-08-18 | Int Minerals & Chem Corp | Beneficiation of potash ores |
| US3282418A (en) * | 1963-10-31 | 1966-11-01 | American Metal Climax Inc | Sylvite recovery process |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3544282A (en) * | 1966-12-06 | 1970-12-01 | Richard Burr | Simplified pretreatment for coarse flotation |
| US3976251A (en) * | 1973-12-19 | 1976-08-24 | Financial Mining - Industrial And Shipping Corporation | Separation of magnesite from its contaminants by reverse flotation |
| US5057208A (en) * | 1984-09-25 | 1991-10-15 | Kali Und Salz Aktiengesellschaft | Method for the production of potassium chloride with K2 O content of more than 55 weight percent |
| US20040144586A1 (en) * | 2003-01-24 | 2004-07-29 | Trott Donald E. | Motorized chariot |
Also Published As
| Publication number | Publication date |
|---|---|
| OA02245A (en) | 1970-05-05 |
| ES328548A1 (en) | 1967-04-01 |
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