US2175093A - Process of concentrating ores by froth flotation - Google Patents
Process of concentrating ores by froth flotation Download PDFInfo
- Publication number
- US2175093A US2175093A US208311A US20831138A US2175093A US 2175093 A US2175093 A US 2175093A US 208311 A US208311 A US 208311A US 20831138 A US20831138 A US 20831138A US 2175093 A US2175093 A US 2175093A
- Authority
- US
- United States
- Prior art keywords
- flotation
- ore
- froth flotation
- agents
- froth
- 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
Links
- 238000009291 froth flotation Methods 0.000 title description 8
- 238000000034 method Methods 0.000 title description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 239000008396 flotation agent Substances 0.000 description 9
- 238000011084 recovery Methods 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000010949 copper Substances 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 238000005188 flotation Methods 0.000 description 4
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002160 Celluloid Polymers 0.000 description 1
- 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 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- -1 aliphatic dicarboxylic acids Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- MMEAFPSLRJDLRM-UHFFFAOYSA-N octadecanedinitrile Chemical compound N#CCCCCCCCCCCCCCCCCC#N MMEAFPSLRJDLRM-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- JTOFSXGLSGTDCB-UHFFFAOYSA-N tetradecanedinitrile Chemical compound N#CCCCCCCCCCCCCC#N JTOFSXGLSGTDCB-UHFFFAOYSA-N 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
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—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
- Y10S209/901—Froth flotation; copper
Definitions
- This invention relates to flotation agents and processes of concentrating ores therewith, and it comprises as new flotation agents aliphatic dinitriles of the general formula NC(CH2)CN,
- froth flotation l0. methods modify the surface of the desired values in' the ore in such a way that the values are floated, leaving the gangue behind.
- aqueous pulp of the ore is first prepared, flotatiorr'agents are added thereto, and the mixture is aerated whereby metalliferous valuesin the ore collect as a froth which can be readily skimmed off and the metal values therein recovered.
- the efl'ectiveness of a flotation agent is largely judged by its ability to separate the various values of the ore and also to separate the metal values one from the other. Some agents require the presence of a frothing agent, such as cresol, etc.,
- aliphatic dinitriles of the general formula NC(CH2)' :cCN are excellent froth flotation agents. This is contarary to some 30 generally accepted beliefs concerning flotation agents since it is the generally held view that compounds containing two polar groups at extreme ends of long carbon chain molecules are ineffective as flotation agents. This is true of 35 aliphatic dicarboxylic acids, their'sodium and potassium salts, etc., but we have discovered that the aliphatic dinitriles are an exception to' this generalization.
- the compounds used by us include sebacodinitrile, plmelodinitrile, adipodini- 40 trile, azelaodinitrile, 1,16-dicyanohexadecane and 1,12-dicyanododecane.
- the following examples can be given to show the effectiveness of these compounds as flotation agents;
- Example 1 versity of Utah flotation cell (capacity 50 grams 7 55 of ore) in such a manner thatall coarse pieces r the same ore,
- potassium ethyl xanthate was used as the flotation agent upon When 0.15 pound per ton of potassium ethyl xanthate and 0.16 pound per ton of cresol are used the recoveries are: copper 70.5%, insoluble 8.3%, and iron 41.1%, which ves a selectivity index of 5.1.
- the potassium pound per ton of ore ethyl xanthate requires a frothing agent, such as cresol, in order to function.
- Example 2 Using the same ore and the experimental conditions as described under Example 1, pimelodinitrile in a concentration of 9.2 pound per ton effects a recovery of 74.8% copper, 61.3% iron and only 3.2% insoluble, giving a selectivity index of 6.2.
- Example 4 An ore containing 6.7% zinc, 3.4% iron and 1.4% lead as sulfides is ground under conditions described in Example 1 and treated with sebacodinitrile in the flotation cell. When a concentration of sebacodinitrlle corresponding to 0.18 is employed the following recoveries are obtained: iron 22.6%, zinc 58.1% and lead 86.5%. When the concentration of sebacodinitrile is increased to 1.7 pounds per ton the following recoveries are obtained: iron 13.6%, zinc 27.8%, and lead 81.3%.
- the step which comprises subjecting to froth flotation an aqueous pulp of the ore containin a mixture of aliphatic dinitriles of the general formula NC(CH2)CN, where :r is at least four.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Oct. 3, 1939 UNITED STATES PATENT OFFICE PROCESS OF CONCENTRATING ORES BY FROTH FLOTATION Anderson W. Ralston and' William 0. Pool, Chicago, Ill., assignors to Armour and Company, Chicago, 111., a corporation of Illinois No Drawing. Application May 16, 1938, Serial No. 208,311
6 Claims.
This invention relates to flotation agents and processes of concentrating ores therewith, and it comprises as new flotation agents aliphatic dinitriles of the general formula NC(CH2)CN,
the concentration of ores by froth flotation l0. methods. These agents modify the surface of the desired values in' the ore in such a way that the values are floated, leaving the gangue behind. Thus, for example, in the froth flotation of ores an aqueous pulp of the ore is first prepared, flotatiorr'agents are added thereto, and the mixture is aerated whereby metalliferous valuesin the ore collect as a froth which can be readily skimmed off and the metal values therein recovered.
20 v The efl'ectiveness of a flotation agent is largely judged by its ability to separate the various values of the ore and also to separate the metal values one from the other. Some agents require the presence of a frothing agent, such as cresol, etc.,
25 while others act as both frothing and collecting agents.
We have discovered that aliphatic dinitriles of the general formula NC(CH2)' :cCN are excellent froth flotation agents. This is contarary to some 30 generally accepted beliefs concerning flotation agents since it is the generally held view that compounds containing two polar groups at extreme ends of long carbon chain molecules are ineffective as flotation agents. This is true of 35 aliphatic dicarboxylic acids, their'sodium and potassium salts, etc., but we have discovered that the aliphatic dinitriles are an exception to' this generalization. The compounds used by us include sebacodinitrile, plmelodinitrile, adipodini- 40 trile, azelaodinitrile, 1,16-dicyanohexadecane and 1,12-dicyanododecane. The following examples can be given to show the effectiveness of these compounds as flotation agents;
Example 1 versity of Utah flotation cell (capacity 50 grams 7 55 of ore) in such a manner thatall coarse pieces r the same ore,
of ore remain in the beaker. Water is added to the contents of the cell until the total amount of water is 200 cc. The cell contents is agitated with an electrically driven stirrer (1700 R. P. M.)
and sebacodinitrile added from a medicine drop- Per, the tip of which has been drawn out to a hair-like capillary. The weight of sebacodini trile per .drop is known by calibration and has been found to be easily reproducible. The amount of sebacodinitrile added to the ore mix- 10 ture in the cell in this experiment is 0.0098 g. The flotation is continued for fifteen minutes, the froth being removed by a Celluloid paddle whenever the froth presents a firm, metallic appearance. This concentrate is received in a beaker and dried to constant weight in an oven at 130 C. The tailing remaining in the flotation cell is also transferred to a beaker and dried at 130 C. The concentrate and tailing are then weighed separately and a 0.5 gram sample of each is analyzed for iron, copper and acid insoluble material. The following are the results which were obtained:
Weight Fe 011 Insoluble.
Grams Percent Percent Percent Concentrate 13.474 33.93 7.40 8.18 Tailing 25.805 9.69 0.82 65.48
Selectivity index 'Cu/Inso1uble=8.5.
' Recoveries Selectiv- 40 Lbs/ton sebacodinitrile 3 542? g ggf Cu Ins. Fe
None 77.6 6.0 54.1 6.3 None 70.2 4.7 54.2 6.9 None 63.2 3.6 40.6 6.8
"For purposes of comparison potassium ethyl xanthate was used as the flotation agent upon When 0.15 pound per ton of potassium ethyl xanthate and 0.16 pound per ton of cresol are used the recoveries are: copper 70.5%, insoluble 8.3%, and iron 41.1%, which ves a selectivity index of 5.1. The potassium pound per ton of ore ethyl xanthate requires a frothing agent, such as cresol, in order to function.
Example 2 Using the same ore and the experimental conditions as described under Example 1, pimelodinitrile in a concentration of 9.2 pound per ton effects a recovery of 74.8% copper, 61.3% iron and only 3.2% insoluble, giving a selectivity index of 6.2.
Example; H
-Using the same ore and experimental conditions as above described a copper recovery of 80.2%, aniron recovery of 58.4% and a silica recovery of 2.8% is obtained with 0.2 pound per ton of 1.12-dicyanododecane. This gives a selectivity index of 7.8.
Example 4 An ore containing 6.7% zinc, 3.4% iron and 1.4% lead as sulfides is ground under conditions described in Example 1 and treated with sebacodinitrile in the flotation cell. When a concentration of sebacodinitrlle corresponding to 0.18 is employed the following recoveries are obtained: iron 22.6%, zinc 58.1% and lead 86.5%. When the concentration of sebacodinitrile is increased to 1.7 pounds per ton the following recoveries are obtained: iron 13.6%, zinc 27.8%, and lead 81.3%.
We have given examples using pure dinitriles as flotation agents only for purposes of illustration. Mixtures of the above described dlnitriles can, of course, be employed and we do not wish to be limited to the use of pure dinitriles. Also we have shown, as in Example 1, that these dinitriles may be mixed with frothing agents if desirable.
Having thus described our invention, what we claim is: 1
1. The process of concentration metalliferous ores which comprises subjecting the ore to froth flotation separation in the presence of an allphatic dinitrile of the general formula NC (CH2) xCN where x is at least four.
2. In the froth flotation of metalliferous ores the step which comprises subjecting to froth flotation an aqueous pulp of the ore containin a mixture of aliphatic dinitriles of the general formula NC(CH2)CN, where :r is at least four.
3. The process as in claim 1 wherein the dinitrile is sebacodinitrile.
ANDERSON W. RALSTON. WILLIAM O. POOL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US208311A US2175093A (en) | 1938-05-16 | 1938-05-16 | Process of concentrating ores by froth flotation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US208311A US2175093A (en) | 1938-05-16 | 1938-05-16 | Process of concentrating ores by froth flotation |
Publications (1)
Publication Number | Publication Date |
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US2175093A true US2175093A (en) | 1939-10-03 |
Family
ID=22774116
Family Applications (1)
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US208311A Expired - Lifetime US2175093A (en) | 1938-05-16 | 1938-05-16 | Process of concentrating ores by froth flotation |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
US4678561A (en) * | 1982-10-14 | 1987-07-07 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
US20080308466A1 (en) * | 2005-11-22 | 2008-12-18 | Barry Graham Lumsden | Mineral Recovery from Ore |
WO2018172307A1 (en) | 2017-03-23 | 2018-09-27 | Akzo Nobel Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
WO2019076858A1 (en) | 2017-10-20 | 2019-04-25 | Akzo Nobel Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
EP3636346A1 (en) | 2018-10-08 | 2020-04-15 | Nouryon Chemicals International B.V. | Process to treat ores and collector composition therefor |
-
1938
- 1938-05-16 US US208311A patent/US2175093A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
US4589980A (en) * | 1982-10-14 | 1986-05-20 | Sherex Chemical Company, Inc. | Promoters for froth flotation of coal |
US4678561A (en) * | 1982-10-14 | 1987-07-07 | 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 |
US20080308466A1 (en) * | 2005-11-22 | 2008-12-18 | Barry Graham Lumsden | Mineral Recovery from Ore |
WO2018172307A1 (en) | 2017-03-23 | 2018-09-27 | Akzo Nobel Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
WO2019076858A1 (en) | 2017-10-20 | 2019-04-25 | Akzo Nobel Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
US20210197210A1 (en) * | 2017-10-20 | 2021-07-01 | Nouryon Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
US11548012B2 (en) * | 2017-10-20 | 2023-01-10 | Nouryon Chemicals International B.V. | Process to treat metal or mineral ores and collector composition therefor |
EP3636346A1 (en) | 2018-10-08 | 2020-04-15 | Nouryon Chemicals International B.V. | Process to treat ores and collector composition therefor |
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