US2944666A - Ore beneficiation - Google Patents
Ore beneficiation Download PDFInfo
- Publication number
- US2944666A US2944666A US575938A US57593856A US2944666A US 2944666 A US2944666 A US 2944666A US 575938 A US575938 A US 575938A US 57593856 A US57593856 A US 57593856A US 2944666 A US2944666 A US 2944666A
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- US
- United States
- Prior art keywords
- ore
- iron
- ground
- flotation
- oil
- 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.)
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Links
- 238000005456 ore beneficiation Methods 0.000 title description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 61
- 238000000034 method Methods 0.000 claims description 50
- 229910052742 iron Inorganic materials 0.000 claims description 27
- 238000005188 flotation Methods 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 20
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical class [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 9
- 238000009291 froth flotation Methods 0.000 claims description 9
- 238000011084 recovery Methods 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 239000012141 concentrate Substances 0.000 description 16
- 239000000295 fuel oil Substances 0.000 description 8
- 239000004115 Sodium Silicate Substances 0.000 description 7
- 238000007792 addition Methods 0.000 description 7
- 239000000446 fuel Substances 0.000 description 7
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 7
- 229910052911 sodium silicate Inorganic materials 0.000 description 7
- 238000003556 assay Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- 210000002683 foot Anatomy 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 235000012343 cottonseed oil Nutrition 0.000 description 3
- 229910052595 hematite Inorganic materials 0.000 description 3
- 239000011019 hematite Substances 0.000 description 3
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 241000725101 Clea Species 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000182988 Assa Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000792859 Enema Species 0.000 description 1
- 241000612118 Samolus valerandi Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007920 enema Substances 0.000 description 1
- 229940079360 enema for constipation Drugs 0.000 description 1
- 230000003311 flocculating effect Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910001608 iron mineral Inorganic materials 0.000 description 1
- 235000019988 mead Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000010743 number 2 fuel oil Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 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
- B03D1/008—Organic compounds containing oxygen
-
- 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
- B03D1/006—Hydrocarbons
-
- 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
Definitions
- our invention comprises a process for a r 2,944,666 1C resented July 12, 1960 ammour: BENEF'Iic -A Q Fred Henry. Bunge. and: Ivan George Eocrnich, Hibbing,- Minna, assignorsto TheM. AsHHIIMQOIBPaIiY, Clev'e land; Ohio; a-corporationof- Ohio 1 a No Drawing. Filed Apr. 4, 1956, Ser. No. 575,938
- Clalrnssr (Claw-5) This invention relates as indicat'ed'lto the of. ore beneficiation and more specifically. to a. process for separating. iron-oxygen. compounds frormironbearing, ores by Iron ores, immediately. .aret rnined, contain excess quantities of siliceous gangue which make direct 2i the. presence, of a. carboxylic' acid collector and fuel oil, it is foun'd'that these fine sizes of iron are heavily floc culated so that they gather" in heavy blackpmasses, while the fihe sizes of. gan'gue are well. dispersed in the ore.
- the carboxylicacid collector used- may be any one of a number. of crude or refined fatty or resin acids. Crude fatty acids such as tall oil and acidulated cottonseed foots' have been found to be'good collectors to employ in the process of our invention; I The amount of car- .exceedih'glS lbs; per ton of ore.
- said invention comprises thefeatureshereinafter fully described and particularly pointed out in the claims, the following description setting fort-h in'.. detail certain illustrative embodiments of the invention-, these being indicative, however, of-fbut a? few' of 7 the. various ways in which the principle of the invention may be the recovery of iron-oxygen compounds from ironbearing ores which comprises grinding said 1 ore to flotation size in the presence of, Lto. 5 pounds of acarboxylic acid per tonv of solids and l. to 29: ounds: at an' oil.- .per ton of solids, and subjecting the. entire. mass which has thus been ground to froth flotation. t a
- the broad embodiment of our invention' comprisesgrin'ding' the ore in the presence ofthe reagents and subsequently floating the iron constituents thereof from thegangue in: a. bath of'water. Onsome ores we have found it desirable to preliminarily com? grinding the ore in the presence of, more reagents and subjecting the fine ground material to froth flotation.
- Metallurgical results EXAMPLE 3 The sample of material used for this test is known as a specular hematite and was obtained from the Groveland formation. In this example, the collector and fuel oil were added tothe sample at the beginning of the grinding period. The collector used was acidulated cottonseed foots produced by The Southern Cotton Oil Company. In this test no sodium silicate was used.
- the sample used forrthis test was a drill core sample from the formation known as Felch Mountain; The crushed 10'mcsh material was ground in a laboratory rod mill for 15 minutes.
- a process for the recovery of iron-oxygen compounds from iron bearing ores which comprises grinding said ore to flotation size in the presence of 1 to 5 pounds of a fatty acid material per ton of solids and l to 20 pounds of a hydrocarbon oil per ton of solids, and subjecting the entire mass which has thus been ground to froth flotation.
- a process for the recovery of iron-oxygen c0mpounds from iron bearing ores which comprises preliminarily comminuting the ore, fine grinding that portion of ground to froth flotation.
- a process for the recovery of iron-oxygen compounds from iron bearing ores which comprises preliminarily grinding said ore to flotation size in the presence of 1 to 5 pounds of a fatty acid per ton of solids and 1 to 20 pounds of a mineral oil per ton of solids, subjecting the entire mass which has thus been preliminarily ground to froth flotation, and collecting the portion thereof which floats, fine grinding such collected portion in the presence of up to 5 pounds of a fatty acid per ton of solids and up to 20 pounds of a mineral oil per ton of solids, and subjecting'the entire mass which has thus been finely ground to froth flotation to recover as well the iron-oxygen compounds contained in the slimes of said ore.
- hydrocarbon oil is a petroleum oil fraction boiling within the range from 450 to 670 F.
- a process for the recovery of iron-oxygen compounds from hematite ores which comprises grinding said ore to liberation size in the presence'of 1 to 5 poundsof tall'oil per ton of ore and 7 to 10 pounds of a petroleum oil boiling within the range of from 450 to 670 F. per ton of ore, subjecting the entire mass which has thus been ground including the slime fines to froth flotation in water, and collecting the iron-bearing froth which floats;
- a process for the recovery of iron-oxide compounds from iron bearing ores which comprises grinding said ore to flotation size, adding up to 5 pounds of a carboxylic fatty acid and up to 20 pounds of a hydrocarbonaceous oil per ton of solids to the ore simultaneously with the grinding step, flocculating the iron minerals and iron slimes of the ore during the grinding step by said acid and oil additives, and subjecting the entire mass to froth flotation.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
flotation.
employed.
Broadly stated our invention comprises a process for a r 2,944,666 1C resented July 12, 1960 ammour: BENEF'Iic -A Q Fred Henry. Bunge. and: Ivan George Eocrnich, Hibbing,- Minna, assignorsto TheM. AsHHIIMQOIBPaIiY, Clev'e land; Ohio; a-corporationof- Ohio 1 a No Drawing. Filed Apr. 4, 1956, Ser. No. 575,938
13 Clalrnssr (Claw-5) This invention relates as indicat'ed'lto the of. ore beneficiation and more specifically. to a. process for separating. iron-oxygen. compounds frormironbearing, ores by Iron ores, immediately. .aret rnined, contain excess quantities of siliceous gangue which make direct 2i the. presence, of a. carboxylic' acid collector and fuel oil, it is foun'd'that these fine sizes of iron are heavily floc culated so that they gather" in heavy blackpmasses, while the fihe sizes of. gan'gue are well. dispersed in the ore.
In the subsequent flotation of the ground ore,.these. floccul'ated masses of, fine i'ronparticles are carried to the surface in the froth, and. the dispersed gangue particles reniainiin the, tailing. The exact reason. for this flocculation of. the fine iron particles is. not completely understood at. present- However, when the ore. is ground in the presence of the reagents the fine sizes of iron are floated to the surface with. the remainder. of, the. heavy iron concentrates leaving the gangue particles in the tail= ing. For. this reason, it is. not necessary to removev the fine particles from ore treated according to our invention. The fine iron particles are collected in the concentrated iron froth, and the finegangue particles remain in transportation and smelting of the ores economically 1 impractical. For this reason, the ores are generally purified by such; processes. as ,flotationgx Many ore flotation processes have been proposed in the past, both to float the iron constituent of the ore from Zthe gangue and to float the gang'ue from the iron. These processes however, have been very inefficient inconcentrating ores containing high percentages of slimjes. Generallyin. order.
roducts= by ,these processes to produce acceptably pu'r it has been necessar'y to r ve the slirhes from the ore before it 'isfloated. The deslirning operations considerably increase the cost of the finished ore both" cause the deslirning operations ;.themselves require? W 'money'a'nd hecau'selthe.ironiconstituents of thejslimes are lost. e
It is 'therefore,- thelfprincipalobject ofthis ihvention 'to provide a process of ore'flot'a'tiofi ivhereby'substantially the tailings. I
The carboxylicacid collector used-may be any one of a number. of crude or refined fatty or resin acids. Crude fatty acids such as tall oil and acidulated cottonseed foots' have been found to be'good collectors to employ in the process of our invention; I The amount of car- .exceedih'glS lbs; per ton of ore.
- 'One' ofithe oils most. economical and easily. lobtainable" v for use-inthe-process of our'invention isthatllifeferred V l toiby the Yt'radeas' No. 2 fueloil. This oil is a petroleum nastieshaving a boiling point of between 450 and 670 all of the iron content of the ore will be collected with. Q
a minimum quantity of gangue. It is a more particular object of this inventiom to; provideta process of iron ore flotation. wherein. desliming. ofthe one isnot. necessary...
Other objects. and. advantages of the present invention will become. apparent asjthes following description proceeds.
To. the ends, said invention, then, comprises thefeatureshereinafter fully described and particularly pointed out in the claims, the following description setting fort-h in'.. detail certain illustrative embodiments of the invention-, these being indicative, however, of-fbut a? few' of 7 the. various ways in which the principle of the invention may be the recovery of iron-oxygen compounds from ironbearing ores which comprises grinding said 1 ore to flotation size in the presence of, Lto. 5 pounds of acarboxylic acid per tonv of solids and l. to 29: ounds: at an' oil.- .per ton of solids, and subjecting the. entire. mass which has thus been ground to froth flotation. t a
We have foundthat by grindingflironoresin tlie presence of a carboxylic acid; senator and. a'. hydrocarbon oil, substantially all of. the-iron.constituents of the ore may becollected by flotation- Iron orevvhieh has been ground without. reagents has 'ared color. which is char: acteristic of the. dispersed fine sizes.- of. hematite. It is recognized that. known.fiotation;processes do. not produce substantial quantities of gangue; materialis v When the ore is ground accordingto ourmvention in accomplishment. of. the. foregoing. andrelated F. and a flash point of 100 F. The amounts of fuel oil used in the process should be within the range of 1 to 20 lbs; of' oil per ton of solids, and in most cases, we have found that 7 to 10 lbs. of oil per ton of solids is most desirable. I
As indicated abovethe broad embodiment of our invention' comprisesgrin'ding' the ore in the presence ofthe reagents and subsequently floating the iron constituents thereof from thegangue in: a. bath of'water. Onsome ores we have found it desirable to preliminarily com? grinding the ore in the presence of, more reagents and subjecting the fine ground material to froth flotation. I
Concentrationofiron me by prior art processes has necessitated grindingofthe ore to at least approximately 65 mesh; However; We have found that iron particles as largefas 20m'esh may be floated by our process. The
I bestproducts are oh'tained'whe'nthe ore is ground to such an" extent'that' the iron is liberated from'the gangue.
- Grin'dingto 1'00 meshis generally sufl'icientfor the purpose. -O'f"'course,"the degreeofigrinding necessary. to obtain the-bestproduct-varies. with the typeofore being purified. For this reason no specific time limits for grinding can be stated. The required grinding varies for different ores.
Our process can be Varied to a considerable degree within the limits ofIour invention.. It is essential that the ore'be ground in the presence of the carboxylic acid collector and an oil, but otherreagents may beadded to the ore immediately prior to flotation and any of the well-known cleaning and finishing operations may be employedfafter the flotation. We have foundit desirable to add to the ground pulp just prior to flotation a small quantity ofsodium. silicatelor Orzan AH-3.
The following examples are included herein to more particularly illustrate specific methods of practicing our invention on given ores andtoillustrate itsadvantages overprior art processes.
3 EXAMPLE 1 A sample of Mesabi Range rock rejects was crushed to 10 mesh and the -10 mesh material ground in a laboratory rod mill to liberation size. In the grinding operation the sample-was ground for 15 minutes and then the reagent addition of the fuel oil and Aliphat 44B were made to the pulp in the rod mill. The pulp was then ground an additional five minutes with the reagents. The Aliphat 44B is a distilled tall oil produced by General Mills, Inc. After the'sample had been ground in'the presence of the collector and fuel oil, it was diluted to 13% solids. To the diluted pulp was added a small quantity of sodium silicate. Subsequent to the addition of the sodium silicate, a rougher flotation concentrate was skimmed from the flotation cell. The rougher flotation concentrate was then subjected to three cleaning operations to produce a concentrate of an acceptable grade. The test procedure and results obtained are presented in the following table.
Conditions and reagents Conditions 7 Reagents Pounds v V Per Ton Stage of Process Time, Per- Ali- N0. 2 So- Mincent pH phat Fuel dium utes Solids 44B 011 Silicate Red Mill Grind. Rod Mill Grind. Rougher Float-.. 1.Clea.ner. 2Cleaner. 3-Cleaner.
Metallurgical results Assay Percent Distri Product Weight Units button Percent Fe Percent Fe S10; Fe
Heads (Assayed) 36.97 Heads (Ca1eu1atcd) 100. 36. 69 100.0 Rougher Tailing 27. 5. 43 1. 47 4. 01 1 Cleaner Tailing 11.13 11.25 1.25 3. 41 2 Cleaner Tailing 5. 33 21. 53 1. 3. 13 3 Cleaner Tailing 3.09 32. 37 1. 00 2. 73 Concentrate; 53. 35 59. 65 31. 82 86. 72
EXAMPLE 2 Conditions and reagents Conditions Reagents Pounds per 7 Ton Stage of Process Time, Per- No. 2 Sodium Mincent pH Liqro Fuel Silicate utes Solids Oil Red Mill Grind" 67 N atural- 2. 34 8. 22 Rougher Float- 2% 26' 0. 1.Clea.ner 2-01eaner-.. -3-Cleaner..
Metallurgical results EXAMPLE 3 The sample of material used for this test is known as a specular hematite and was obtained from the Groveland formation. In this example, the collector and fuel oil were added tothe sample at the beginning of the grinding period. The collector used was acidulated cottonseed foots produced by The Southern Cotton Oil Company. In this test no sodium silicate was used.
- Conditions and reagents Conditions Reagents Pounds 3 er Ton 1 stage orPi-ocess Acidu- A Time, Percent lated No. 2
Minutes Solids pH Cottoln- Fuel Oil 1 i sec Foots Rod Mill Grind 15 61 Natural 2.20 7.68 Rougher Float 151 26 o 1Oieaner-. 152 do 2Cicaner 13 -do 3-Gleaner 7 o do Metallurgical results Assay Percent Distri- Product Weight Units bution Percent Fe Percent Fe S10, Fe
Heads (Assayed) 34. 97 :Heads (Calculate .00 g 35.05 100. 00 Rougher Tailing- .52 l 5.88 1. 91 5.45 l Cleaner Tailing .09 12. 65 1.15 3. 28 2 Cleaner 'Iaxlmg.- .10 21. O6 0.86 2. 45 .3 Cleaner Tailing .26 28. 49 0. 64 1. 83 Concentrate 03 58.60 30; i9 86. 99
7 EXAMPLE 4:
The sample used forrthis test was a drill core sample from the formation known as Felch Mountain; The crushed 10'mcsh material was ground in a laboratory rod mill for 15 minutes. The collector, Aliphat 44E,
a product of General Mills, Inc., and fuel oil additions were then made to the pulp in the rod .mill and the sample ground with the reagents 'for. an additional five minutes. The ground sample which had been conditioned "with they above-mentioned reagents during the last stages of the grind was pulped with water in -a laboratory flotation cell and a sodium silicate addition made to the pulp. A rougher concentrate was then removed by skimming the froth from the cell. In like manner, the rougher concentrate was cleaned threetimes by repulping with tap waters Sodium silicate additions were made to the first and second cleaner circuits I Conditions and reagents Reagents names EXAMPLE 6 r I A pplicat iono f summaries process to the large remetallurgical results obtained on the 1% inch *Halobe Cmditim serves of non-magnetic taconite found on the Mesabi PerTon Y y e a 5 Range is .shown' n Examples 6 and 7. The non-magnetic S a Process taconite sample used in these testswas obtained from the Time, Per- Ah: No.2 ,So; 7
I w v Mincent, pH phat: Fuel dium property known as West Patrick. In th s example,.the utes Sdlds' 44E on l f crushed 10 mesh material was ground in a lahoiatory rod mill for 20 minutes. The collector Liqro, which is M2 U a crude tall oil, and fuel oil additions were then made to RodM111Gr1nd t R'ougher Float the pulp in the rod-mllland the pulp ground an additional 1C1eaner fi e minutes with the reagents. The ground sample was 2-C1eaner H ,7 3-C1aner .hen pulped 1n a laboratory flotation cell and a sodium H I 'licate addition made to the pulp. 'The rougherfroth Metallurgical r'esults a t en k d, ro the flotation c :I 1;? enj 15 ner, the rougher concentrate was cleaned three t-i neshy T Assay-Percent. EM. repulp-mg with tap 'water. I Addit onal sodium silicate Product .Weight Units bution was added to the first and second cleaning circuits.
Percent A v Fe Percent V k V t e y Bfe s10; n r Fe I M Conditions and reagents V Heads (Assayed) 32. 72 Conditions Reagents Pounds per Heads (Calcu1ated) 100.00 32; 91 100. 00 a Ton Rougher Tailing 31.44 4:62 71. 15' -,4:41 x T 1 Cleaner Tailin 12.00 10.86 1.30 3.95 Stege'of Process I Y 1 2C1eanerTaili1w. 5.99 21.71 1.30 3.95 Time, .Per-
1 No.2 Sodium 3'C1eaner'1ailing. 3.40 31.42 $1. 07 3. Mincent pH Liqro Fuel Silicate Concentrate..- 1 47.17 58.91 27.79 84.44 25 utes Solids Oil 5 7 Rod'MillGrinnL. 2e 60 A d 9 salaried i i" 94 Rod Mill Grind.-- a Y 60 1.11 8.96 I Y a 26, 0.50 r lProdu't Fe I'SiQ "oao Mg 0 Mn- 1,03 P enemas. 60:70 6.70 2'66" 104i 0:50 0:12'
N a w -Mjet qllurgical results H EXAMPLE F 72.; 'Assay iei'cent Distri- '1:he invention is further described m this example 1 22533, si .ggggg where the process has beenapplied to various size frac- Fe 810, v Fe none of Mesabi Range ores which are tdo're'fractory fto be concentrated effectively by the conventional gravity 7 i methods which arefnowu'sed. Fo1-"e'Xamplethe 1 /zinch sagg- 93;;33 natural size particlesofanore'identif ed"as'Halobe when 40, 1 Cleane rfIaihng. 1o; 62 1.173 crushed "to /2" and "concentrated by the "conventional .Q l 1 v H n V I 3C1eanerTa1lin 0.51 1.42 heavy media method produced 'aconcentrate which as- Concentrate 33.46 93.39 sayed 54.00 percent iron'and2 2f73 Pereentsilica. I -Iow- 'e\ er, whena sample of the 1 /2' inch naturalsizeiparticies EXAMPLE 7 or the "or was crushed and -"ground t'o flotation; size and 45 The test shown in "this "example *is a duplicate "of "Ex- 'arnple 6 except that slightly decreased quantities of fatty acid and fuel'oil were used The conditions, reagents used, and metallurgical results of the test are presented ore 'is'p-resented in the followingftab'ulafion. 'imthe'fol'lowing table- Conditions anar 'az'hts i qi i s'ii d' Conditions I ii t'eaen ts i loundsber Conditions 'R-ehlgent-sqgglindsvpier Stage of Process Stage of Pwcess Ti P 'Time, 'Per- H No.2 Sodium g: g; H L1 qio 3 'Min- :cent -pH Liqro Fuel Silicate utes Solids- I, f: a. F W. 011 Rod M111 Grind; 20 in -Natural 2.54.. 8.22- 33 333g" 2 Rougher Float... 2 26'.' do 0.50 Rougher mead 2 -1Cleaner 2 do 0. 50
l 1 Cleaner.-. 2 2Cleaner 2 0.25 koleaner; 2 v 2 9- '3 Cieai1er 2 .M iq ht kd r tt et M ll r lts 7,
. Assay Per nt Distriv Assay Percent Distil- Product Weight Units bution Product Weight Unitsbution Percent v Fe .Percent Percent v Fe 7 Percent m l e S10; 7 n iie Fe SiOz Fe Heads (Assayed) I Heads (Assa y'ed) HeadsiCalculate 100.00 100.00 Heads (Calculated) 100.00 100; 00 Rougher Tailing 23. 15 .2. 65 Rougher Tailing 30. 83 '2. 91 1 Cleaner Telling.-. 10. 49 ,2. 59 1 Cleaner Tailing 11.77 3.00 2 Cleaner Tailing... 5.43 2. 21 2 Cleaner Tai1ing. 5.18 2. 91 -15 Cleaner 'iailing 3. 13 2.00 3 Cleaner Tailing.. 2. 89 .2555 Concentrate 57 90. 55 1 Concentrate 49. 33 88. 63
tional petroleum sulfonate process.
7 COMPARATIVE EXAMPLE OF PRIOR ART In order to further illustrate the improved results that .vention, a testwas conducted using the known conven- The test using the petroleum sulfonate procedure was performed on a sample of the same ore which was used in the test described in Example 1. It is well known that in order for the sulfonate process to function satisfactorily the fine sizes of ground ore frequently referred to as slimes must be first removed in order that their adverse effect on the subsequent flotation operation will be eliminated. The procedure and results obtained with the sulfonate process are presented in the following table. In conducting this test the 10 mesh ore was ground for 20 minutes in a rod mill. After grinding the sample was pulped to 20% solids, the fines were dispersed with sodium silicate and that an iron concentrate of an acceptable grade would be produced.
Conditions and reagents Conditions Reagents Pounds Per Ton Stage of Process Time, Per- Rea- Sul- Sod.
Mincent pH gent Fuel phur- Siliutes Solids 899 Oil ic cate Acid Rod Mill Grind.-- 20 .67 Deslime (2 times). 3 20 6. Condition 3 50 5. 0 3. 76 7. 0 Rougher Float..- 2 4 0 1Oleaner 2 2Cleaner 2 3-Oleaner 2 M ezallurgzcal results Assay Percent Distri- Product Weight Units bution Percent Fe Percent Fe SiO, Fe
Heads (assayed) 36.97 Heads (calculated) 100.00 37.67 100.00 Slime 81. 28 31. 33 9. 80 26.08 Rougher Tailing 10. 48 7. 55 0.79 2. 1 Cleaner Tailin 11.04 10. O6 1. 11 2. 95 2 Gleaner Tailin 5. 8B 22. 87 1. 34 3. 57 3 Cleaner Tailin 5. 04 41. 90 35 78 2.11 5. 62 Concentrate 36. 30 61. 76 7 33 22. 42 59. 68 Concentrate and3 Oleaner Tailing 41. 34 59. 34 10. 79 24. 53 65.30
In comparing the results obtained withthe new process described in this invention with the results obtained with V a known conventional process, it is clearly seen that a ven ere a Pre semi ar s bst nt l y all of the iron in the original ore. The product of our process is substantially pure so that undue costs of shipping and smelting a large quantity of siliceous gangue are not incurred. In our process, the slimes, i.e. fine particles in the ground ore need not be removed from the ore before flotation. In the flotation operation, the iron constituents of the slimes are collected in the finished product and the gangue constituents of the slimes arev left behind in the tailings.
Other modes of applying the principle of the invention may be employed, change being made as regards the details described, provided the features stated in any of the following claims or the equivalent of such be employed.
We, therefore, particularly point out and distinctly claim as our invention:
l. A process for the recovery of iron-oxygen compounds from iron bearing ores which comprises grinding said ore to flotation size in the presence of 1 to 5 pounds of a fatty acid material per ton of solids and l to 20 pounds of a hydrocarbon oil per ton of solids, and subjecting the entire mass which has thus been ground to froth flotation.
2. The process of claim 1 characterized further in that said ore is ground to such an extent that 95% thereof will pass a 20 mesh screen.
3. A process for the recovery of iron-oxygen c0mpounds from iron bearing ores which comprises preliminarily comminuting the ore, fine grinding that portion of ground to froth flotation.
4. The process of claim 3 characterized further in that said ore is comminuted to such an extent that 95% thereof will pass a 20 mesh screen, and the preliminarily com- -minuted ore which contains all of the fines is finely ground to such an extent that 95% thereof will pass a 100 mesh screen.
5. A process for the recovery of iron-oxygen compounds from iron bearing ores which comprises preliminarily grinding said ore to flotation size in the presence of 1 to 5 pounds of a fatty acid per ton of solids and 1 to 20 pounds of a mineral oil per ton of solids, subjecting the entire mass which has thus been preliminarily ground to froth flotation, and collecting the portion thereof which floats, fine grinding such collected portion in the presence of up to 5 pounds of a fatty acid per ton of solids and up to 20 pounds of a mineral oil per ton of solids, and subjecting'the entire mass which has thus been finely ground to froth flotation to recover as well the iron-oxygen compounds contained in the slimes of said ore.
6. The process'of claim 5 characterized further in that said ore is' preliminarily ground to such an extent that thereof will pass a 20 mesh screen and said collected portion is ground to such an extent that 95% thereof will pass a mesh screen.
7. The process of claim 1 characterized further in that said fatty acid material is a resin acid.
8. The process of claim 1 characterized further in that said fatty acid material is tall oil.
9. The process of claim 1 characterizedfurther in that said fatty acid material is acidulated cottonseed foots. 10. The process of claim 1 characterized further in that I said hydrocarbon oil is a mineral oil.
11. The process of claim 1 characterized further in that said hydrocarbon oil is a petroleum oil fraction boiling within the range from 450 to 670 F.
12. A process for the recovery of iron-oxygen compounds from hematite ores which comprises grinding said ore to liberation size in the presence'of 1 to 5 poundsof tall'oil per ton of ore and 7 to 10 pounds of a petroleum oil boiling within the range of from 450 to 670 F. per ton of ore, subjecting the entire mass which has thus been ground including the slime fines to froth flotation in water, and collecting the iron-bearing froth which floats;
13. A process for the recovery of iron-oxide compounds from iron bearing ores which comprises grinding said ore to flotation size, adding up to 5 pounds of a carboxylic fatty acid and up to 20 pounds of a hydrocarbonaceous oil per ton of solids to the ore simultaneously with the grinding step, flocculating the iron minerals and iron slimes of the ore during the grinding step by said acid and oil additives, and subjecting the entire mass to froth flotation.
'10 References Cited in the file of this patent UNITED STATES PATENTS 2,014,406 Weed Sept. 17, 1935 2,563,447 Alsop Aug. 7, 1951 2,669,355 Archibald Feb. 16, 1954 OTHER REFERENCES Taggart: Handbook of Mineral Dressing," Wiley 1945, pp. 12-88.
Claims (1)
1. A PROCESS FOR THE RECOVERY OF IRON-OXYGEN COMPOUNDS FROM IRON BEARING ORES WHICH COMPRISES GRINDING SAID ORE TO FLOTATION SIZE IN THE PRESENCE OF 1 TO 5 POUNDS OF A FATTY ACID MATERIAL PER TON OF SOLIDS AND 1 TO 20 POUNDS OF A HYDROCARBON OIL PER TON SOLIDS, AND SUBJECTING THE ENTIRE MASS WHICH HAS THUS BEEN GROUND TO FROTH FLOTATION.
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US575938A US2944666A (en) | 1956-04-04 | 1956-04-04 | Ore beneficiation |
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US575938A US2944666A (en) | 1956-04-04 | 1956-04-04 | Ore beneficiation |
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US575938A Expired - Lifetime US2944666A (en) | 1956-04-04 | 1956-04-04 | Ore beneficiation |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3033364A (en) * | 1958-09-05 | 1962-05-08 | Weston David | Treatment and recovery of material by flotation |
US3067957A (en) * | 1959-09-08 | 1962-12-11 | Cleveland Cliffs Iron | Process of upgrading iron ore concentrates |
US3268071A (en) * | 1962-08-22 | 1966-08-23 | Ca Nat Research Council | Process for the separation of solids by agglomeration |
US3405802A (en) * | 1964-07-20 | 1968-10-15 | Phosphate Dev Corp Ltd | Flotation of apatite |
US3589622A (en) * | 1967-04-24 | 1971-06-29 | David Weston | Flotation of metallic oxides iii |
US3847357A (en) * | 1971-02-16 | 1974-11-12 | D Weston | Separation of copper minerals from pyrite |
US4193791A (en) * | 1976-10-28 | 1980-03-18 | Reynolds Metals Company | Concentration of hydrated aluminum oxide minerals by flotation |
US4316797A (en) * | 1980-09-10 | 1982-02-23 | Phillips Petroleum Company | Flotation agent and process |
US4424123A (en) | 1982-08-12 | 1984-01-03 | Phillips Petroleum Company | Ore flotation using fulvenes |
EP0106787A2 (en) * | 1982-10-14 | 1984-04-25 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
US4504385A (en) * | 1982-12-30 | 1985-03-12 | Sherex Chemical Company, Inc. | Ester-alcohol frothers for froth flotation of coal |
US4744891A (en) * | 1986-05-12 | 1988-05-17 | Nalco Chemical Company | Flotation of apatite from magnatite |
US20070184987A1 (en) * | 1996-07-24 | 2007-08-09 | Brandbury Andrew J | Additive for increasing the density of an oil-based fluid and fluid comprising such additive |
WO2008077849A1 (en) * | 2006-12-22 | 2008-07-03 | Akzo Nobel N.V. | Amine formulations for reverse froth flotation of silicates from iron ore |
US20160377860A1 (en) * | 2013-11-25 | 2016-12-29 | Kyocera Corporation | Lens unit, imaging apparatus, and on-vehicle camera |
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US2014406A (en) * | 1932-10-12 | 1935-09-17 | Weed Floyd | Method of concentrating nonsulphide minerals by froth flotation |
US2563447A (en) * | 1951-08-07 | Flotation of hematite | ||
US2669355A (en) * | 1950-07-05 | 1954-02-16 | United States Steel Corp | Flotation method and reagent |
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US2563447A (en) * | 1951-08-07 | Flotation of hematite | ||
US2014406A (en) * | 1932-10-12 | 1935-09-17 | Weed Floyd | Method of concentrating nonsulphide minerals by froth flotation |
US2669355A (en) * | 1950-07-05 | 1954-02-16 | United States Steel Corp | Flotation method and reagent |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3033364A (en) * | 1958-09-05 | 1962-05-08 | Weston David | Treatment and recovery of material by flotation |
US3067957A (en) * | 1959-09-08 | 1962-12-11 | Cleveland Cliffs Iron | Process of upgrading iron ore concentrates |
US3268071A (en) * | 1962-08-22 | 1966-08-23 | Ca Nat Research Council | Process for the separation of solids by agglomeration |
US3405802A (en) * | 1964-07-20 | 1968-10-15 | Phosphate Dev Corp Ltd | Flotation of apatite |
US3589622A (en) * | 1967-04-24 | 1971-06-29 | David Weston | Flotation of metallic oxides iii |
US3847357A (en) * | 1971-02-16 | 1974-11-12 | D Weston | Separation of copper minerals from pyrite |
US4193791A (en) * | 1976-10-28 | 1980-03-18 | Reynolds Metals Company | Concentration of hydrated aluminum oxide minerals by flotation |
US4316797A (en) * | 1980-09-10 | 1982-02-23 | Phillips Petroleum Company | Flotation agent and process |
US4424123A (en) | 1982-08-12 | 1984-01-03 | Phillips Petroleum Company | Ore flotation using fulvenes |
US4589980A (en) * | 1982-10-14 | 1986-05-20 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
EP0106787A2 (en) * | 1982-10-14 | 1984-04-25 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
EP0106787A3 (en) * | 1982-10-14 | 1986-03-26 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
US4504385A (en) * | 1982-12-30 | 1985-03-12 | Sherex Chemical Company, Inc. | Ester-alcohol frothers for froth flotation of coal |
US4744891A (en) * | 1986-05-12 | 1988-05-17 | Nalco Chemical Company | Flotation of apatite from magnatite |
US20070184987A1 (en) * | 1996-07-24 | 2007-08-09 | Brandbury Andrew J | Additive for increasing the density of an oil-based fluid and fluid comprising such additive |
US20070287637A1 (en) * | 1996-07-24 | 2007-12-13 | Bradbury Andrew J | Additive for increasing the density of an oil-based fluid and fluid comprising such additive |
US7538074B2 (en) | 1996-07-24 | 2009-05-26 | M-I L.L.C. | Additive for increasing the density of an oil-based fluid and fluid comprising such additive |
US20090275487A1 (en) * | 1996-07-24 | 2009-11-05 | Bradbury Andrew J | Additive for increasing the density of an oil-based fluid and fluid comprising such additive |
WO2008077849A1 (en) * | 2006-12-22 | 2008-07-03 | Akzo Nobel N.V. | Amine formulations for reverse froth flotation of silicates from iron ore |
US20160377860A1 (en) * | 2013-11-25 | 2016-12-29 | Kyocera Corporation | Lens unit, imaging apparatus, and on-vehicle camera |
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