US2914174A - Phosphate mineral beneficiation process - Google Patents
Phosphate mineral beneficiation process Download PDFInfo
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- US2914174A US2914174A US705765A US70576557A US2914174A US 2914174 A US2914174 A US 2914174A US 705765 A US705765 A US 705765A US 70576557 A US70576557 A US 70576557A US 2914174 A US2914174 A US 2914174A
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- amine
- residue
- fatty acids
- reaction mixture
- phosphate
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- 238000000034 method Methods 0.000 title claims description 21
- 229910052585 phosphate mineral Inorganic materials 0.000 title description 12
- 150000001412 amines Chemical group 0.000 claims description 58
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 19
- 239000000194 fatty acid Substances 0.000 claims description 19
- 229930195729 fatty acid Natural products 0.000 claims description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- 150000004665 fatty acids Chemical class 0.000 claims description 18
- 238000009291 froth flotation Methods 0.000 claims description 18
- 238000009835 boiling Methods 0.000 claims description 17
- 238000003786 synthesis reaction Methods 0.000 claims description 16
- 230000015572 biosynthetic process Effects 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 13
- 239000011541 reaction mixture Substances 0.000 claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 10
- 239000010452 phosphate Substances 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 239000003760 tallow Substances 0.000 claims description 9
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 description 21
- -1 fuel oil Chemical class 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 238000005188 flotation Methods 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 239000012141 concentrate Substances 0.000 description 10
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical group CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- 239000002367 phosphate rock Substances 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- BWZOPYPOZJBVLQ-UHFFFAOYSA-K aluminium glycinate Chemical compound O[Al+]O.NCC([O-])=O BWZOPYPOZJBVLQ-UHFFFAOYSA-K 0.000 description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 239000003549 soybean oil Substances 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- 238000010693 amine synthesis reaction Methods 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 238000005406 washing Methods 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
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- 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
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/02—Collectors
-
- 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
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
- B03D2203/06—Phosphate ores
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S209/00—Classifying, separating, and assorting solids
- Y10S209/902—Froth flotation; phosphate
Definitions
- This invention relates to the concentration of phosphate Un t t s minerals by froth flotation. More specifically, the invention relates to a froth flotation process effective, inter alia, to separate silica from phosphate minerals.
- Phosphate rock normally occurs in association wit silica as a major gangue constituent.
- the phosphate inand economical methods for the production of a phosphate rock concentrate having a minimum silica content, preferably not more than about 3% or 4% by weight. a
- the first flotation stage, deslimed raw rock feed is conditioned with caustic soda, a hydrocarbon such as fuel oil, or kerosene, and a fatty acid reagent such as tall oil and thereafter subjected to froth flotation in conventional manner to yield a phosphate product commonly called a rougher concentrate.
- the rougherconcentrate normally contains from about 8% to about 20% by weight of silica and hence is a low grade phosphate material of limited value. Accordingly, the rougher concentrate is conventionally freed of reagents or deoiled by scrubbing with a mineral acid such as sulfuric acid and deslimed in preparation for a second stage of froth flotation concentration.
- the de-oiled, deslirned rougher concentrate is frequently designated as amine flotation feed by reason of the strong cationic amine collecting agents which are conventionally employed in the second froth flotation stage in which the silica is floated and discharged to waste.
- the underflow from the second stage is high phosphate concentrate which is transferred to storage.
- the amine collecting agents useful in the second or amine flotation stage are eflicient and yield a satisfactory It is an additional object of the invention to provide a process for the concentration of phosphate minerals by the two-stage flotation technique which is at least as eflicient and substantially less expensive then similar processes now commercially employed.
- Amines conventionally used as collectors in froth flotaabout 20 carbon atoms are conventionally used as collectors in froth flotaabout 20 carbon atoms.
- silica containing phosphate'minerals can be efficiently concentrated by froth flotation in the presence of a collecting agent comprising the residue normally resulting from the separation, from acrude product of the synthesis of an aliphatic amine containing from about eight to about twenty carbon atoms, of a fraction having a boiling point lower than that of said residue and containing a substantial portion ofjat least one aliphatic amine having from about eight to about twenty carbon atoms, and recovering a phosphate concentrate.
- a collecting agent comprising the residue normally resulting from the separation, from acrude product of the synthesis of an aliphatic amine containing from about eight to about twenty carbon atoms, of a fraction having a boiling point lower than that of said residue and containing a substantial portion ofjat least one aliphatic amine having from about eight to about twenty carbon atoms, and recovering a phosphate concentrate.
- the amine residues are useful as collection agents regardless of the primary purpose for which the lower boiling amine fraction is
- the invention generically embraces utilization of collectors comprising amine residues of all types in the froth flotation of phosphate minerals. It will be appreciated that the composition of such amine residues will vary, for example, with the particular method of amine synthesis utilized, the starting materials employed, the end point of the lower boiling fraction which may be removed, and thelike.
- the utility of the amine residues in the invention changes only in degree with such variations and materials and conditions and the invention therefore contemplates utilization of all residues from the synthesis of aliphatic amines containing from about eight to about twenty carbon atoms and mixtures thereof.
- the preferred amine residues are formed by the reduction of about eight to about twenty carbon atom fatty acids followed by the separation of an amine fraction containing not more than about eighteen carbon atoms.
- Particularly appropriate starting materials which yield the preferred amine residues comprise natural mixtures of fatty acids such as coconut oil fatty acids, tallow fatty acids and soy bean oil fatty acids.
- the invention further contemplates utilization of the I amine residues in combination with conventional amine collectors. Indeed, in some cases it may be appropriate to blend the various amine residues which may be avail able with conventional aliphatic amine collectors to produce a reagent of more uniform characteristics. Optimum results in certain cases have been achieved by utilization of a mixture of the residues resulting from the commercial preparation of amines derived from natural fatty acid mixtures with from about 20% to about 40% by weight of the corresponding lower boiling amine fraction.
- the invention in its generic embodiment embraces a utilization of all collectors comprising amine residues and hence in cludes the utilization in the froth flotation concentration of phosphate minerals of the entire crude product of the synthesis of aliphatic amines containing from about eight to about twenty carbon atoms.
- the amine residue containing flotation collectors of this invention are employed in' conventional manner'and in conventional proportions known to the art and described inter alia in US. Patents 2,293,640 and 2,724,501.
- the amine residue collection agents of this invention are partially neutralized by the addition of an appropriate mineral or organic acid such as hydrochloric acid or acetic to facilitate solution in water and to provide a pulp having a pH of from about 7 to about 8.
- the amine residue reagents of the invention are employed in proportions requisite to provide from about 0.4 pound to about 1.5 pound of reagent per ton of ore treated.
- the particular proportions utilized do not constitute the essence of the invention.
- the optimum quantity of amine will vary to a minor degree with the specific reagent utilized and can readily be determined by expedients well known to those skilled in the art.
- EXAMPLE I A sample of rougher concentrate formed by the fatty acid beneficiation of deslimed Florida phosphate rock in a commercial phosphate rock concentration plant was scrubbed with sulfuric acid in conventional manner to yield a substantially reagent free feed appropriate for second stage froth flotation concentration with an amine collector. The sample was divided into eleven aliquot portions for comparative testing.
- a commercial amine collector composed of a mixture of equal parts by volume of a butyl amine and Alamine 26, a commercial amine product formed by the reduction of tallow acids followed by fractionation of the crude reduction product to yield a material containing approximately 30% by weight hexadecyl amines, 45% by weight octadecyl amine and 25% by weight octadecenyl amine.
- the present invention provides a process which is effective materially to reduce the cost of the froth flotation concentration of phosphate minerals and accordingly constitutes a significant contribution to the art.
- Representative amines include octyl, nonyl, decyl, decenyl, isodecyl, dodecyl, 'isododecyl, dodecenyl, tetradecyl, hexadecyl, hexadecenyl, 1 isohexadecenyl, and octadecyl amine; and mixtures thereof.
- a process for the beneficiation of a silica containing phosphate ore which comprises subjecting said ore to froth flotation in the presence of a collector consisting of a high boiling amine residue produced by (a) synthesis of mixed amines by reduction of a natural fatty acid mixture selected from the group consisting of the coconut oil fatty acids, the tallow fatty acids, and the soy bean fatty acids; and (b) removing from the crude synthesis reaction mixture the amines containing not more than about eighteen carbon atoms; the residue of said reaction mixture remaining after the removal of said fraction constituting said collector and consisting essentially of mixed amines containing more than eighteen carbon atoms together with materials present in said crude reaction mixture which have a boiling point in excess of the terminal boiling point of said removed fraction.
- the improvement which comprises utilizing as a collector in said second flotation stage a residue consisting of a high boiling amine residue produced by (a) synthesis of mixed amines by reduction of a natural fatty acid mixture selected from the group consisting of the coconut oil fatty acids, the tallow fatty acids, and the soy bean fatty acids; and (b) removing from the crude synthesis reaction mixture the amines containing not more than about eighteen carbon atoms; the residue of said reaction mixture remaining after the removal of said fraction constituting said collector and consisting References Cited in the file of this patent UNITED STATES PATENTS Crago Aug. 18, 1942 Lentz Dec. 17, 1957
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Description
PHOSPHATE MINERAL BENEFICIATION PROCESS Joseph F. Haseman, Lakeland, Fla, assignor to Internation of New York No Drawing. Application December 30, 1957 a Serial No. 705,765
8 Claims. (Cl. 209-166) This invention relates to the concentration of phosphate Un t t s minerals by froth flotation. More specifically, the invention relates to a froth flotation process effective, inter alia, to separate silica from phosphate minerals. a. Phosphate rock normally occurs in association wit silica as a major gangue constituent. The phosphate inand economical methods for the production of a phosphate rock concentrate having a minimum silica content, preferably not more than about 3% or 4% by weight. a
.. Conventional practice, particularly in the Florida phosdustry has devoted substantialetio'rt to devise efiicient phate industry, employs a phosphate mineral concentra tion process pursuant to which a rough concentration is etfected by washing or desliming and the final concentration is achieved by two stages of froth flotation. In
the first flotation stage, deslimed raw rock feed is conditioned with caustic soda, a hydrocarbon such as fuel oil, or kerosene, and a fatty acid reagent such as tall oil and thereafter subjected to froth flotation in conventional manner to yield a phosphate product commonly called a rougher concentrate. The rougherconcentrate normally contains from about 8% to about 20% by weight of silica and hence is a low grade phosphate material of limited value. Accordingly, the rougher concentrate is conventionally freed of reagents or deoiled by scrubbing with a mineral acid such as sulfuric acid and deslimed in preparation for a second stage of froth flotation concentration. The de-oiled, deslirned rougher concentrate is frequently designated as amine flotation feed by reason of the strong cationic amine collecting agents which are conventionally employed in the second froth flotation stage in which the silica is floated and discharged to waste. The underflow from the second stage is high phosphate concentrate which is transferred to storage.
The amine collecting agents useful in the second or amine flotation stage are eflicient and yield a satisfactory It is an additional object of the invention to provide a process for the concentration of phosphate minerals by the two-stage flotation technique which is at least as eflicient and substantially less expensive then similar processes now commercially employed.
It is a more specific object of the invention to provide a novel collector for use in the second or amine stage of a conventionaltwo stage froth flotation procedure for the concentration of phosphate minerals.
Amines conventionally used as collectors in froth flotaabout 20 carbon atoms.
, 2,914,174 Patented New 24, 1959 thesis reaction mixture which is fractionated to provide a relatively lower boiling amine material for use inter alia, as a froth flotation collector and a relatively-higher boil- ,ing bottoms fraction or residue. Various well known methods of synthesis are employed including reduction o'f'the corresponding fatty acids, amination of the corresponding halogenated hydrocarbons, and the like. Regardless of the method of synthesis employed, it has generally been considered necessary to separate a comparatively lower boiling amine product fraction for' use as a flotation collector from a relatively higher boiling residue portion of the amine synthesis reaction mixture.
Now, in accordance with this invention, ithas been discovered that silica containing phosphate'minerals can be efficiently concentrated by froth flotation in the presence of a collecting agent comprising the residue normally resulting from the separation, from acrude product of the synthesis of an aliphatic amine containing from about eight to about twenty carbon atoms, of a fraction having a boiling point lower than that of said residue and containing a substantial portion ofjat least one aliphatic amine having from about eight to about twenty carbon atoms, and recovering a phosphate concentrate. It will be appreciated that the amine residues are useful as collection agents regardless of the primary purpose for which the lower boiling amine fraction is prepared or utilized.
The invention generically embraces utilization of collectors comprising amine residues of all types in the froth flotation of phosphate minerals. It will be appreciated that the composition of such amine residues will vary, for example, with the particular method of amine synthesis utilized, the starting materials employed, the end point of the lower boiling fraction which may be removed, and thelike. The utility of the amine residues in the invention changes only in degree with such variations and materials and conditions and the invention therefore contemplates utilization of all residues from the synthesis of aliphatic amines containing from about eight to about twenty carbon atoms and mixtures thereof. The preferred amine residues are formed by the reduction of about eight to about twenty carbon atom fatty acids followed by the separation of an amine fraction containing not more than about eighteen carbon atoms. Particularly appropriate starting materials which yield the preferred amine residues comprise natural mixtures of fatty acids such as coconut oil fatty acids, tallow fatty acids and soy bean oil fatty acids.
'The invention further contemplates utilization of the I amine residues in combination with conventional amine collectors. Indeed, in some cases it may be appropriate to blend the various amine residues which may be avail able with conventional aliphatic amine collectors to produce a reagent of more uniform characteristics. Optimum results in certain cases have been achieved by utilization of a mixture of the residues resulting from the commercial preparation of amines derived from natural fatty acid mixtures with from about 20% to about 40% by weight of the corresponding lower boiling amine fraction. The invention in its generic embodiment embraces a utilization of all collectors comprising amine residues and hence in cludes the utilization in the froth flotation concentration of phosphate minerals of the entire crude product of the synthesis of aliphatic amines containing from about eight to about twenty carbon atoms. a
The amine residue containing flotation collectors of this invention are employed in' conventional manner'and in conventional proportions known to the art and described inter alia in US. Patents 2,293,640 and 2,724,501. In general, and in accordance with conventional practice, the amine residue collection agents of this invention are partially neutralized by the addition of an appropriate mineral or organic acid such as hydrochloric acid or acetic to facilitate solution in water and to provide a pulp having a pH of from about 7 to about 8. The amine residue reagents of the invention are employed in proportions requisite to provide from about 0.4 pound to about 1.5 pound of reagent per ton of ore treated. The particular proportions utilized do not constitute the essence of the invention. The optimum quantity of amine will vary to a minor degree with the specific reagent utilized and can readily be determined by expedients well known to those skilled in the art.
It will be appreciated by those skilled in the art that the froth flotation concentration of phosphate minerals entails problems difierent from those which attend concentration of metallic ores by the same physical process. Hence reagents useful in metallic ore concentration may prove quite inappropriate for phosphate mineral beneficiation.
The following examples illustrate the best mode presently known for the practice of the invention.
EXAMPLE I A sample of rougher concentrate formed by the fatty acid beneficiation of deslimed Florida phosphate rock in a commercial phosphate rock concentration plant was scrubbed with sulfuric acid in conventional manner to yield a substantially reagent free feed appropriate for second stage froth flotation concentration with an amine collector. The sample was divided into eleven aliquot portions for comparative testing.
Five percent by volume water emulsions of the following amine reagents were prepared using two parts by weight of kerosene for each part by weight of amine reagent.
(1) A commercial amine collector composed of a mixture of equal parts by volume of a butyl amine and Alamine 26, a commercial amine product formed by the reduction of tallow acids followed by fractionation of the crude reduction product to yield a material containing approximately 30% by weight hexadecyl amines, 45% by weight octadecyl amine and 25% by weight octadecenyl amine.
(2) A product similar to 1, supplied by the Harshaw Chemical Company under the trade name Uvermene 38.
(3) A residue remaining after the separation of a lower boiling amine fraction similar to Alamine 26 from an amine product formed by the reduction of tallow acids, and supplied by Armour and Company under the trade name Armeen Residue (Tallow).
(4) A residue remaining after the separation of a lower boiling amine fraction from an amine product formed by the reduction of coconut oil fatty acids and supplied by Armour and Company under the trade name Armeen Residue (Cocoa)."
(5) A residue remaining after the separation of a lower boiling amine fraction from an amine product formed by the reduction of soy bean oil fatty acids and supplied by Armour and Company under the trade name Armeen Residue (Soy bean).
(6) A mixed residue believed to be generally com.- parable to a mixture of equal parts of reagent 3 and reagent 5 and supplied by General Mills under the trade name Alamine 60.
(7) A mixed amine residue comparable to reagent No. 6 supplied by Armour and Company under the trade name Armeen Residue.
(8) A mixture comprised of 80% by weight of reagent No. 7 and 20% by weight of tallow amines supplied by Armour and Company under the trade name of Armeen T.1
(9) A reagent similar to reagent No. 8 but containing 60% by weight of amine residue and 40% by weight of Ar-meen T.
(10) A mixture similar to reagent No. 8 but containing 40% by weight of amine residue and 60% by weight of Armeen T, and supplied by Armour and Company.
(11) A reagent believed to be similar to reagent No. 8 but containing about equal parts by weight of amine residue and Armeen T and supplied by Armour and Company under the trade name Mixed Crude Armeen Lot 5593.
All emulsions are neutralized to a pH of 7.0 which corresponds to approximately 75% neutralization of the total amine. The feed was conditioned at about 25% solids and subjected to froth flotation in a 500 gram Denver laboratory flotation cell in which the Phosphate concentrate was recovered from the underflow and the silica tail was floated, in conventional manner with the results as indicated in Table I.
Table I.-Appr0ximate amine reagent cost for optimum flotation with various amines Approxi- Grade and Recovery mate Cost/T. Amine Cost/Lb. Lbs/Ton Amine Reagent FOB In Feed Feed,
No. Tank Required Cents BPL Oars, Cents BPL Insol. Ree,
Percent The present invention provides a process which is effective materially to reduce the cost of the froth flotation concentration of phosphate minerals and accordingly constitutes a significant contribution to the art.
It will be appreciated that the specific amine synthesis reaction mixtures from which the amine residue flotation agents are derived does not constitute an essential or critical feature of the invention which extends to the utilization of residues from the synthesis of all saturated and unsaturated, straight and branched chain aliphatic amines containing from about eight to about twenty carbon atoms. Representative amines include octyl, nonyl, decyl, decenyl, isodecyl, dodecyl, 'isododecyl, dodecenyl, tetradecyl, hexadecyl, hexadecenyl, 1 isohexadecenyl, and octadecyl amine; and mixtures thereof.
I claim:
1. A process for the beneficiation of a silica containing phosphate ore which comprises subjecting said ore to froth flotation in the presence of a collector consisting of a high boiling amine residue produced by (a) synthesis of mixed amines by reduction of a natural fatty acid mixture selected from the group consisting of the coconut oil fatty acids, the tallow fatty acids, and the soy bean fatty acids; and (b) removing from the crude synthesis reaction mixture the amines containing not more than about eighteen carbon atoms; the residue of said reaction mixture remaining after the removal of said fraction constituting said collector and consisting essentially of mixed amines containing more than eighteen carbon atoms together with materials present in said crude reaction mixture which have a boiling point in excess of the terminal boiling point of said removed fraction.
2. The process of claim 1 wherein said crude synthesis product is produced by the reduction of tallow fatty acids.
3. The process of claim 1 wherein said crude synthesis product is produced by the reduction of soy bean oil fatty acids.
4. The process of claim 1 wherein said crude synthesis product is produced by the reduction of coconut oil fatty acids.
5. In a process for the concentration of phosphate minerals by a two-stage froth flotation procedure in which a rougher concentrate is produced in the first flotation stage, and a final concentrate produced in the second flotation stage, the improvement which comprises utilizing as a collector in said second flotation stage a residue consisting of a high boiling amine residue produced by (a) synthesis of mixed amines by reduction of a natural fatty acid mixture selected from the group consisting of the coconut oil fatty acids, the tallow fatty acids, and the soy bean fatty acids; and (b) removing from the crude synthesis reaction mixture the amines containing not more than about eighteen carbon atoms; the residue of said reaction mixture remaining after the removal of said fraction constituting said collector and consisting References Cited in the file of this patent UNITED STATES PATENTS Crago Aug. 18, 1942 Lentz Dec. 17, 1957
Claims (1)
1. A PROCESS FOR THE BENEFICIATION OF A SILICA CONTAINING PHOSPHATE ORE WHICH COMPRISES SUBJECTING SAID ORE TO FROTH FLOTATION IN THE PRESENCEOF A COLLECTOR CONSISTING OF A HIGH BOILING AMINE RESIDUE PRODUCED BY (A) SYNTHESIS OF MIXED AMINES BY REDUCTION OF A NATURAL FATTY ACID MIXTURE SELECTED FROM THE GROUP CONSISTING OF THE COCONUT OIL FATTY ACIDS, THE TALLOW FATTY ACIDS, AND THE SOY BEAN FARRY ACIDS; AND (B) REMOVING FROM THE CRUDE SYNTHESIS REACTION MIXTURE THE AMINES CONTAINING NOT MORE THAN ABOUT EIGHTEEN CARBON ATOMS; THE RESIDUE OF SAID REACTION MIXTURE REMAINING AFTER THE REMOVAL OF SAID FRACTION CONSTITUTING SAID COLLECTOR AND CONSISTING ESSENTIALLY OF MIXED AMINES CONTAINING MORE THAN EIGHTEEN CARBON ATOMS TOGETHER WITH MATERIAL PRESENT IN SAID CRUDE REACTION MIXTURE WHICH HAVE A BOILING POINT IN EXCESS OF THE TERMINAL BOILING POINT OF SAID REMOVED FRACTION.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US705765A US2914174A (en) | 1957-12-30 | 1957-12-30 | Phosphate mineral beneficiation process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US705765A US2914174A (en) | 1957-12-30 | 1957-12-30 | Phosphate mineral beneficiation process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2914174A true US2914174A (en) | 1959-11-24 |
Family
ID=24834840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US705765A Expired - Lifetime US2914174A (en) | 1957-12-30 | 1957-12-30 | Phosphate mineral beneficiation process |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2914174A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3073448A (en) * | 1960-10-28 | 1963-01-15 | Armour & Co | Ore flotation collector and ore flotation process |
| US3114704A (en) * | 1961-04-20 | 1963-12-17 | Armour & Co | Ore flotation collector and ore flotation process |
| US3129166A (en) * | 1961-06-30 | 1964-04-14 | Int Minerals & Chem Corp | Ore beneficiation process and agent |
| US3179250A (en) * | 1961-07-31 | 1965-04-20 | Armour & Co | Separating finely-divided minerals |
| US3404777A (en) * | 1965-05-07 | 1968-10-08 | Armour & Co | Froth flotation with secondary-alkyl primary amines |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2293640A (en) * | 1940-10-08 | 1942-08-18 | Phosphate Recovery Corp | Process of concentrating phosphate minerals |
| US2816870A (en) * | 1954-07-19 | 1957-12-17 | Gen Mills Inc | Dispersible fatty amines |
-
1957
- 1957-12-30 US US705765A patent/US2914174A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2293640A (en) * | 1940-10-08 | 1942-08-18 | Phosphate Recovery Corp | Process of concentrating phosphate minerals |
| US2816870A (en) * | 1954-07-19 | 1957-12-17 | Gen Mills Inc | Dispersible fatty amines |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3073448A (en) * | 1960-10-28 | 1963-01-15 | Armour & Co | Ore flotation collector and ore flotation process |
| US3114704A (en) * | 1961-04-20 | 1963-12-17 | Armour & Co | Ore flotation collector and ore flotation process |
| US3129166A (en) * | 1961-06-30 | 1964-04-14 | Int Minerals & Chem Corp | Ore beneficiation process and agent |
| US3179250A (en) * | 1961-07-31 | 1965-04-20 | Armour & Co | Separating finely-divided minerals |
| US3404777A (en) * | 1965-05-07 | 1968-10-08 | Armour & Co | Froth flotation with secondary-alkyl primary amines |
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