US2458523A - Froth flotation of sulfide ores in the presence of a n-dichlorothiocarbanilide - Google Patents
Froth flotation of sulfide ores in the presence of a n-dichlorothiocarbanilide Download PDFInfo
- Publication number
- US2458523A US2458523A US620648A US62064845A US2458523A US 2458523 A US2458523 A US 2458523A US 620648 A US620648 A US 620648A US 62064845 A US62064845 A US 62064845A US 2458523 A US2458523 A US 2458523A
- Authority
- US
- United States
- Prior art keywords
- froth flotation
- ore
- dichlorothiocarbanilide
- sulfide ores
- ores
- 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
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 title description 6
- 239000010949 copper Substances 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 238000005188 flotation Methods 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000003963 dichloro group Chemical group Cl* 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 150000004763 sulfides Chemical group 0.000 description 2
- GWEHVDNNLFDJLR-UHFFFAOYSA-N Carbanilide Natural products C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229910016006 MoSi Inorganic materials 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical class C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241001251753 Riparia cincta Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- -1 dichloro thiocarbanilide Chemical compound 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229910052961 molybdenite Inorganic materials 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- B03D1/012—Organic compounds containing sulfur
-
- 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
- This invention relates to the concentration of ores and has for an object the provision of certain improvements in concentration operations. More particularly, the invention contemplates the provision of certain improvements in flotationagitated with 10 c. c. of sodium hydroxide. 20
- the flotation reagent may be employed advantageously in neutral, alkaline and acid circuits. It may be employed advantageously in froth flotation operations designed for the concentration of both non-metallic minerals and metallic minerals and in froth flotation operations designed for the concentration of both oxidized ores and sulphide ores.
- the reagent can be employed with particular advantage in froth flotation operations designed for the concentration of sulphide ores.
- the following examples illustrate the advantages of the reagent of the invention over reagents employed heretofore.
- the ore employed in the 'tests was Braden Copper Company ore containing on the average about 2.16% copper in sulphide form and about 0.21% copper in non-sulphide form and containing small amounts (about 0.075%) of molybdenite (M032).
- the ore was ground to 2.5% plus IOU-mesh in all cases.
- Example 1 Total Concta, per Tails, 1. r Recoveries, Mineral Cob LIL/um cost of cent cent percent lectors Req'd I ore Cu Mos, Cu M08 Cu M05;
- the standard reagent referred to in Example 1 56 is a well-known mineralcollecting agent (ethyl 3 xanthogen ethylformate) accepted at the time of the tests as being the most effective in treating the ore tested, and the amounts indicated were the amounts considered to be most suitable.
- ethyl 3 xanthogen ethylformate a well-known mineralcollecting agent accepted at the time of the tests as being the most effective in treating the ore tested, and the amounts indicated were the amounts considered to be most suitable.
- the method of concentrating sulphide ore which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of a chlorinated thiocar-banilide comound in which a chloride atom is attached to a nitrogen atom.
- the method of concentrating sulphide ore which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of dichloro thiocarbanilide in which chlorine atoms are attached to nitrogen atoms.
- CHECIN ⁇ C S CaHLCIN v RHETHERFORD B. MARTIN.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Jan. 11, 1949 IUNITTEDSTATES PATENT orrics FROTH FLOTATION' F SULFIDEv ORES IN THE PRESENCE OF A N-DICHLOROTHIO- CARBANILIDE Rhetheri'ord B. Martin, New York, N. Y., assignor to Kennecott Copper Corporation, New York, N. Y., a corporation ofNew York No Drawing. Application October 5, 1945, Serial No. 620,648
3 Claims. (Cl. 209-166) This invention relates to the concentration of ores and has for an object the provision of certain improvements in concentration operations. More particularly, the invention contemplates the provision of certain improvements in flotationagitated with 10 c. c. of sodium hydroxide. 20
The flotation reagent may be employed advantageously in neutral, alkaline and acid circuits. It may be employed advantageously in froth flotation operations designed for the concentration of both non-metallic minerals and metallic minerals and in froth flotation operations designed for the concentration of both oxidized ores and sulphide ores. The reagent can be employed with particular advantage in froth flotation operations designed for the concentration of sulphide ores.
The following examples illustrate the advantages of the reagent of the invention over reagents employed heretofore. The ore employed in the 'tests was Braden Copper Company ore containing on the average about 2.16% copper in sulphide form and about 0.21% copper in non-sulphide form and containing small amounts (about 0.075%) of molybdenite (M032). The ore was ground to 2.5% plus IOU-mesh in all cases.
Example 1 Total Concta, per Tails, 1. r Recoveries, Mineral Cob LIL/um cost of cent cent percent lectors Req'd I ore Cu Mos, Cu M08 Cu M05;
,19. 681 18 015 92. 36 81.28 Standard 16 1 24 24. 03 645 24 .025 89. 76 69. 76 l6 13. 70 550 .11 019 95. 72 83. 88 1. 148 24. 15 644 22 025 90. 64 69. 93 1. I153 17. 20 617 14 014 94. 63 86. 10 I16 .151 5186' .756 .21 .024 01. 05' 69.
Ez'ample z Total Concta, per Tails, per Recoveries, Mineral COL Lb'lbon cost of cent cent percent lectors Req'd 525 ore Cu MoSi Cu M081 Cu M08:
18. 60 650 14 022 94. 40 78. 93 Dichloro thiccarbanilid. 10 071 24. 80 750 42 028 82. 43 68'. 04 Do i0 18. 611 13 015 94. 83. 65 NaCl 1. 50 095 24. 40 617 30 02S 87. 58 65. 63 Dichloro thiocarbanilid- 10 17. 75 638 15 016 94. 05 84. 21 NaOl i. 50 Kerosene 16 0976 24.15 789 25 020 89. 37 77. 43
No solid was at first precipitated, but, after the addition of 20 c. c. of water and again shaking. mm-dichlorothio-carbanilide was obtained in quantitative yield.
This method of preparing the compound is described in the Journal of the Society of Chemical Industry, vol. 45, 1926, page 351T.
The upper figures in the above tables indicate 50 results obtained with Fagergren flotation machines, and the lower figures indicate results obtained with Minerals Separation flotation machines.
The standard reagent referred to in Example 1 56 is a well-known mineralcollecting agent (ethyl 3 xanthogen ethylformate) accepted at the time of the tests as being the most effective in treating the ore tested, and the amounts indicated were the amounts considered to be most suitable.
I claim:
1. The method of concentrating sulphide ore which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of a chlorinated thiocar-banilide comound in which a chloride atom is attached to a nitrogen atom.
2. The method of concentrating sulphide ore which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of dichloro thiocarbanilide in which chlorine atoms are attached to nitrogen atoms.
3. The method of concentrating sulphide ore which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of a compound having the following structural formula:
CHECIN \C=S CaHLCIN v RHETHERFORD B. MARTIN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Certificate of Correction Patent No. 2,458,523. January 11, 1949.
RI-IETHERFORD B. MARTIN It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows:
Column 3 line 10 claim 1 for the Word chloride read chlorine;
and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Oflice.
Signed and sealed this 31st day of May, A. D. 1949.
[sun] THOMAS F. MURPHY,
Assistant Oommz'ssz'oner of Patents.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US620648A US2458523A (en) | 1945-10-05 | 1945-10-05 | Froth flotation of sulfide ores in the presence of a n-dichlorothiocarbanilide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US620648A US2458523A (en) | 1945-10-05 | 1945-10-05 | Froth flotation of sulfide ores in the presence of a n-dichlorothiocarbanilide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2458523A true US2458523A (en) | 1949-01-11 |
Family
ID=24486771
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US620648A Expired - Lifetime US2458523A (en) | 1945-10-05 | 1945-10-05 | Froth flotation of sulfide ores in the presence of a n-dichlorothiocarbanilide |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2458523A (en) |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1364308A (en) * | 1919-03-25 | 1921-01-04 | Metals Recovery Co | Flotation of minerals |
| US1610217A (en) * | 1925-04-24 | 1926-12-07 | Du Pont | Process of concentrating ores by flotation |
| US2061243A (en) * | 1932-08-24 | 1936-11-17 | Du Pont | Unsymmetrical fluoro-phenyl-thioureas and process of preparing same |
| US2106552A (en) * | 1936-03-30 | 1938-01-25 | Monsanto Chemicals | Thiocarbanilide derivatives |
| US2139697A (en) * | 1937-07-09 | 1938-12-13 | Du Pont | Thiourea derivatives |
| US2336464A (en) * | 1941-07-18 | 1943-12-14 | Burroughs Wellcome Co | Urea and thiourea derivatives |
-
1945
- 1945-10-05 US US620648A patent/US2458523A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1364308A (en) * | 1919-03-25 | 1921-01-04 | Metals Recovery Co | Flotation of minerals |
| US1610217A (en) * | 1925-04-24 | 1926-12-07 | Du Pont | Process of concentrating ores by flotation |
| US2061243A (en) * | 1932-08-24 | 1936-11-17 | Du Pont | Unsymmetrical fluoro-phenyl-thioureas and process of preparing same |
| US2106552A (en) * | 1936-03-30 | 1938-01-25 | Monsanto Chemicals | Thiocarbanilide derivatives |
| US2139697A (en) * | 1937-07-09 | 1938-12-13 | Du Pont | Thiourea derivatives |
| US2336464A (en) * | 1941-07-18 | 1943-12-14 | Burroughs Wellcome Co | Urea and thiourea derivatives |
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