US1774183A - Concentration of minerals - Google Patents
Concentration of minerals Download PDFInfo
- Publication number
- US1774183A US1774183A US191262A US19126227A US1774183A US 1774183 A US1774183 A US 1774183A US 191262 A US191262 A US 191262A US 19126227 A US19126227 A US 19126227A US 1774183 A US1774183 A US 1774183A
- Authority
- US
- United States
- Prior art keywords
- flotation
- concentration
- sulfide
- ore
- copper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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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
-
- 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
- the sulfides em loyed as flotation agents 5 or adjuvants in t e process of the present invention are those represented by the formula R -S R wherein R and R stand for the same or difierent alkyl or aralkyl lydrocarbon radicals or grouss such asCH 2'0 2 H5, 03H C4H9, C5H11, 5H5;CH et/c-, and w si nifies the number 1 or a number greater t an 1.
- the group ,-S is attached or bound on each side to a saturated aliphatic carbon atom.
- the disulfides as represented by the formula 1. RSSR where R and R stand for the same or similar alkyl or aralkyl groups are particularly important, and especially those which contain no nitrogen in their composition.
- the sulfides employed in the present invention can be prepared in any 1 suitable or well-known manner such as, for
- halogen derivative of a hydrocarbon in which the halogen is bound to a saturated aliphatic carbon, on a metal sulfide or polysulfide; by the oxidation of mercaptans wherein the mercapto oup, SH, is bound to an aliphatic caron atom; by the decomposition by chemical or electrolytic means of the salts of an alkyl-or an aralkyl-thiosulfuric acid; and by dissolving sulfur in the lower sulfides to form the higher or polysulfides. They may be used as flotation agents in the pure Application filed Kay 13, 1927. Serial No. 191,262.
- the flotation agent comprislng the sulfide belonging to or related to the aliphatic series may be incorporated with the ore or the mineral pulp in any sultable manner and at any suitable time WlIICh will insure a satisfactory flotation operatlon.
- it may be introduced in the free state or it may be dissolved, suspended or, dispersed in any suitable solvent or dispersing agent such as, for example, water, or one or more of the usual flotation oils or oil mixtures, or in a suitable organlc solvent or medium, and incorporating the resulting solution, suspension or dispersion with the ore or ore pulp.
- the agents of the present invention show marked action as flotation agents in ore concentration, some of them also exhibit considerable frothing properties and others not. Ordinarily, they are used to advantage in conjunction with a suitable frot-hing agent, e. g., pine oil, crude turpentine, terpineol, tar acids, etc. They are sometimes used also to-advantage in admixture with each other or in conjunction with other flotation agents, and are particularly valuable when used in conjunction or in admixture with a mercaptan, such as a thioalcohol or a thiophenol, I
- a suitable frot-hing agent e. g., pine oil, crude turpentine, terpineol, tar acids, etc.
- a mercaptan such as a thioalcohol or a thiophenol
- the rocess of the present invention may be carried out in any suitable apparatus, for example, those of the pneumatic type such as the Callow cell, or those Where the air is incorporated with the mixture by mechanical agitation such as the J anney apparatus, or the like.
- the alkali may be caustic alkali such as caustic soda or an alkaline salt such as soda ash, or it may be calcium oxide or hydrate, etc.
- the amount of flotation agent required to be used in the flotation process will vary, it depending artly on the character and composition of the ore, partly on the particular sulfide employed, 1 and partly on other factors.
- Example 2 500 parts of a copper ore (of the Anaconda Copper Company) assaying 1.52 percent copper was treated as in Example 1 except 0.0625 parts of.n-butyl monosulfide was used in place of dibenzyl disulfide. 68.1 parts of concentrate assaying 10.05 percent copper was obtained which is a recovery of 90.6 percent. The tai'lings assayed 0.16 percentcopper. It may be mentioned that n-butyl monosulfide possesses considerable frothing qualities and may be employed without the use of an additional frothing agent.
- the present invention contemplates the utilization as flotation agents in the separation of minerals and the concentration -of ores of those sulfides and polysulfides wherein sulfur is attached to a saturated aliphatic carbon atom; that said flotation agents may be incorporated in or with the ore or mineral pulp at any suitable time and in any suitable manner; that they may be used in the free state or in ad mixture with one another or in solution, suspension or dispersion in any suitable solvent or medium; and that they may be used in conjunction with other flotation agents or with frothing agents, orwith both.
- the present invention is applicable to the treatment of various kinds of mineral mixtures, both natural and artificial, which are amenable to concentration by flotation processes.
- alkyl and aralkyl denote hydrocarbon radicals, that is, radicals composed only of carbon and hydrogen in their composition.
- the process which comprises mixing with-a co per sulfide ore pulp a sulfide of the ro able formula, RS,-R' wherein-R an R stand for the same or different alk l or aralkyl h drocarbon radicals and a: has a value 0 one or more, and subjecting the resulting mixture to a froth flotation operation.
- the process wlilch comprises subjecting a copper sulfide ore pulp to a froth flotation o eration in the presence of a sulfide of the probable formula.
Description
Patented Aug. 26, 1930 UNITED STATES PATENT OFFICE FREDERICK G. MOSES OF NEW YORK, RAYMOND W. HESS, OF BUFFALO, AND ROBERT L. PERKINS, OF EAST AURORA, NEW YORK, ASSIGNORS TO THE BARRETT COMPANY, OF NEW YORK, N. Y., A CORPORATION OF NEW JERSEY CONCENTRATION OF MINERALS No Drawing.
ores b carrying out the flotation operationwith t e addition to the mineral pul to the of a sulfide belonging to or relat aliphatic series. I
The sulfides em loyed as flotation agents 5 or adjuvants in t e process of the present invention are those represented by the formula R -S R wherein R and R stand for the same or difierent alkyl or aralkyl lydrocarbon radicals or grouss such asCH 2'0 2 H5, 03H C4H9, C5H11, 5H5;CH et/c-, and w si nifies the number 1 or a number greater t an 1. In these sulfides, the group ,-S is attached or bound on each side to a saturated aliphatic carbon atom. The disulfides as represented by the formula 1. RSSR where R and R stand for the same or similar alkyl or aralkyl groups are particularly important, and especially those which contain no nitrogen in their composition.
In general, the sulfides employed in the present invention can be prepared in any 1 suitable or well-known manner such as, for
example, by the action of a halogen derivative of a hydrocarbon, inwhich the halogen is bound to a saturated aliphatic carbon, on a metal sulfide or polysulfide; by the oxidation of mercaptans wherein the mercapto oup, SH, is bound to an aliphatic caron atom; by the decomposition by chemical or electrolytic means of the salts of an alkyl-or an aralkyl-thiosulfuric acid; and by dissolving sulfur in the lower sulfides to form the higher or polysulfides. They may be used as flotation agents in the pure Application filed Kay 13, 1927. Serial No. 191,262.
or purified state; and, in general, they may I): talso employed in the crude or impure s a e. 4
In carrying outthe flotation process of the present invention, the flotation agent comprislng the sulfide belonging to or related to the aliphatic series may be incorporated with the ore or the mineral pulp in any sultable manner and at any suitable time WlIICh will insure a satisfactory flotation operatlon. For example, it may be introduced in the free state or it may be dissolved, suspended or, dispersed in any suitable solvent or dispersing agent such as, for example, water, or one or more of the usual flotation oils or oil mixtures, or in a suitable organlc solvent or medium, and incorporating the resulting solution, suspension or dispersion with the ore or ore pulp. vWhile the agents of the present invention show marked action as flotation agents in ore concentration, some of them also exhibit considerable frothing properties and others not. Ordinarily, they are used to advantage in conjunction with a suitable frot-hing agent, e. g., pine oil, crude turpentine, terpineol, tar acids, etc. They are sometimes used also to-advantage in admixture with each other or in conjunction with other flotation agents, and are particularly valuable when used in conjunction or in admixture with a mercaptan, such as a thioalcohol or a thiophenol, I
in which they dissolve to form a liquid.
The rocess of the present invention may be carried out in any suitable apparatus, for example, those of the pneumatic type such as the Callow cell, or those Where the air is incorporated with the mixture by mechanical agitation such as the J anney apparatus, or the like.
It is of advantage in many cases, as with certain copper ores, to subject the ore pulp to the action of an amount of alkali suflicient to give it a neutral or an alkaline reaction before subjecting it to flotation with the aid of the flotation agents of the present invention. The alkali may be caustic alkali such as caustic soda or an alkaline salt such as soda ash, or it may be calcium oxide or hydrate, etc.
In the differential separation of various minerals, such as zinc blende from associated minerals, the presence of an alkali cyanide, or of copper sulfate or other salts, is sometimes advantageous. I
The amount of flotation agent required to be used in the flotation process will vary, it depending artly on the character and composition of the ore, partly on the particular sulfide employed, 1 and partly on other factors.
Ordinarily, one-fifth to one-half pound of the flotation agent per ton of ore will be sufficient, but larger or smaller amounts than this may be required.
The invention will be further illustrated by the following specific example. The parts are by weight.
Example: 500 parts of a copper sulfide ore (of Miami Copper Company) assayin 1.22 percent copper was ground in a ball mill with 220 parts water, 0.0625 parts of dibenzyl disulfide,
. tically' all of the mixture was sufliciently fine to pass a 40 mesh screen. The ground pulp was diluted with water to give a mixture containing about 16 percent solidsand subject ed to flotation in a J anney flotation apparatus. After agitating for two or three minutes, a small amount of pine oil, e, g., about 0.02 to 0.03 parts, was added. A satisfactory mineral froth was produced. During the next 20 minutes of agitation, a further amount of pine oil was added, suflicient to make a total of about 0.06 to 008- parts. Mechanical agitation of the pulp was-continued for about 5 minutes after all the pine oil was added. 24.9 parts of concentrate assaying 17.2 per cent copper was obtained which is a recovery of 69. percent of copper. The tailings assayed 0.38 percent copper. It will be noted that the equivalent of about 20.3 tons of ore was required to give 1 ton of concentrate.
In a similar test using 500 parts of an Anaconda copper ore analyzing 152 percent copper, and employing 0.0625 parts of isoamyl disulfide in place of dibenzyl disulfide, there was obtained 46.4 parts concentrate assaying 15.3 percent copper which is a recovery of 93.5 percent copper.
Example 2: 500 parts of a copper ore (of the Anaconda Copper Company) assaying 1.52 percent copper was treated as in Example 1 except 0.0625 parts of.n-butyl monosulfide was used in place of dibenzyl disulfide. 68.1 parts of concentrate assaying 10.05 percent copper was obtained which is a recovery of 90.6 percent. The tai'lings assayed 0.16 percentcopper. It may be mentioned that n-butyl monosulfide possesses considerable frothing qualities and may be employed without the use of an additional frothing agent.
In a similar test on the same ore except that 0.0625 parts of allyl monosulfide was used in place of isoamyl disulfide there was obtained 49.2 parts concentrate assaying 13.7 percent copper whichis a recovery of 89.5 percent. ()ther flotation agents, such as ethyl monosulfide, n-propyl monosulfide, isopropyl monosulfide, isoam l monosulfide, benzyl monosulfide, ethyl isulfide, n-propyl disulfide, isopropyl disulfide, and n-butyl disulfide, have been found to give analogous results. In general, the disulfides effect a better separation than thinonosulfides.
It will thus be noted that the present invention contemplates the utilization as flotation agents in the separation of minerals and the concentration -of ores of those sulfides and polysulfides wherein sulfur is attached to a saturated aliphatic carbon atom; that said flotation agents may be incorporated in or with the ore or mineral pulp at any suitable time and in any suitable manner; that they may be used in the free state or in ad mixture with one another or in solution, suspension or dispersion in any suitable solvent or medium; and that they may be used in conjunction with other flotation agents or with frothing agents, orwith both.
It will be understood that the present invention is applicable to the treatment of various kinds of mineral mixtures, both natural and artificial, which are amenable to concentration by flotation processes.
It will be further understood that the invention is not limited in this specification to the use of the particular agents or other ingredients mentioned in the example, and that other agents, particularly other flotation1 agents of the class mentioned, can be use In the specification and claims, the terms alkyl and aralkyl denote hydrocarbon radicals, that is, radicals composed only of carbon and hydrogen in their composition.
We claim:
1. In effecting the concentration of minerals by flotation, the process which comprises mixing with the mineral pulp a sulfide of the probable formula R S R' wherein R and R stand for the same or different alkyl or aralkyl hydrocarbon radicals and 00 has a value of 1 or more, and subjecting the resulting mixture to a froth flotation operation.
2. In efi'ectingthe concentration of minerals by flotation, the process which comprises ind mixing with the mineral pulp a sulfide of the probable formula RS R Where R and R stand for an alkyl hydrocarbon or aralkyl group and a: has a value of 2 or more, and subjecting the resulting mixture to. a froth flotation o eration.
3. In e ecting the concentration of minerals by flotation, the process which comprises subjecting a mineral pulp to a froth flotation operation in the presence of a sulfide of the probable formula RSS--R wherein R and R stand for the same or different alkyl or aralkyl hydrocarbon radicals.
4. In efi'ecting the concentration of minerals by flotation, the process which comprises subjecting a mineral pulp to a froth flotation ogeration in the presence of dibenzyl disulfi e.
5. In effecting the concentration of minerals by flotation, the process which comprises subjecting the mineral in the form of an alkaline pulp to a froth flotation operation in the presence of an organic sulfide having the following probable formula: RS,.R where R and R stand for the same or different alkyl or aralkyl hydrocarbon radicals and a: has a value of 1 or more.
6. In effecting the concentration of ores by flotation, the process which comprises subjecting the ore in the form of a suitable pulp to a froth flotation operation in the presence of a diaralkyl pol sulfide, the diaralkyl radical containing on y carbon and hydrogen in its composition.
7. In effecting the concentration of minerals by flotation, the process which comprises subjecting a mineral pulp to a froth flotation operation in the presence of a sulfide having the following probable formula: RS R where a: has a value of 1 or more, and R and R stand for the same or different aralkyl hydrocarbon radicals.
8. In effecting the concentration of ores by flotation, the process which comprises subjecting an ore pulp to a froth flotation o eration in the presence of a sulfide embo ying within its composition the probable grouping where a: has a value of 1 or more, and said groupin being attached on each side to a saturate aliphatic carbon atom of a hydrocarbon radical.
9. In effecting the concentration of copper sulfide ores by flotation, the process which comprises mixing with-a co per sulfide ore pulp a sulfide of the ro able formula, RS,-R' wherein-R an R stand for the same or different alk l or aralkyl h drocarbon radicals and a: has a value 0 one or more, and subjecting the resulting mixture to a froth flotation operation.
10. In effecting the concentration of co per sulfide ores by otation, the process wlilch comprises subjecting a copper sulfide ore pulp to a froth flotation o eration in the presence of a sulfide of the probable formula.
to a froth flotation operation in the presence of dibenzyl disulfide.
In testimony whereof we aflix our signatures.
FREDERICK G. MOSES. RAYMOND W. HESS. ROBERT L. PERKINS.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US191262A US1774183A (en) | 1927-05-13 | 1927-05-13 | Concentration of minerals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US191262A US1774183A (en) | 1927-05-13 | 1927-05-13 | Concentration of minerals |
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US1774183A true US1774183A (en) | 1930-08-26 |
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US191262A Expired - Lifetime US1774183A (en) | 1927-05-13 | 1927-05-13 | Concentration of minerals |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2429617A1 (en) * | 1978-06-27 | 1980-01-25 | Elf Aquitaine | Flotation collectors esp. for sulphide minerals - comprise organic thio cpds. esp. alkyl thio ethanol(s) (SW 28.1.80) |
US4274950A (en) * | 1978-06-27 | 1981-06-23 | Societe Nationale Elf Aquitaine (Production) | Process for the flotation of sulfide ores |
FR2534493A1 (en) * | 1982-10-13 | 1984-04-20 | Elf Aquitaine | ENRICHMENT OF ORES BY FLOTATION AND COLLECTING AGENTS EMPLOYED THEREFOR |
FR2534492A1 (en) * | 1982-10-13 | 1984-04-20 | Elf Aquitaine | IMPROVEMENT IN MINERAL FLOTATION |
WO1986006983A1 (en) * | 1985-05-31 | 1986-12-04 | The Dow Chemical Company | Novel collectors for the selective froth flotation of sulfide minerals |
US4676890A (en) * | 1985-11-29 | 1987-06-30 | The Dow Chemical Company | Collector compositions for the froth flotation of mineral values |
US4735711A (en) * | 1985-05-31 | 1988-04-05 | The Dow Chemical Company | Novel collectors for the selective froth flotation of mineral sulfides |
US9505011B1 (en) * | 2015-12-28 | 2016-11-29 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as mining chemical collectors |
US9512071B1 (en) | 2015-12-28 | 2016-12-06 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US9512248B1 (en) | 2015-12-28 | 2016-12-06 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
WO2018027046A1 (en) * | 2016-08-04 | 2018-02-08 | Chevron Phillips Chemical Company Lp | Mining collector compositions containing dodecylmethyl sulfide and processes for the recovery of metals therewith |
US10011564B2 (en) | 2015-12-28 | 2018-07-03 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US10040758B2 (en) | 2015-12-28 | 2018-08-07 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US10294200B2 (en) | 2015-12-28 | 2019-05-21 | Chevron Phillips Chemical Company, Lp | Mixed branched eicosyl polysulfide compositions and methods of making same |
-
1927
- 1927-05-13 US US191262A patent/US1774183A/en not_active Expired - Lifetime
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2429617A1 (en) * | 1978-06-27 | 1980-01-25 | Elf Aquitaine | Flotation collectors esp. for sulphide minerals - comprise organic thio cpds. esp. alkyl thio ethanol(s) (SW 28.1.80) |
US4274950A (en) * | 1978-06-27 | 1981-06-23 | Societe Nationale Elf Aquitaine (Production) | Process for the flotation of sulfide ores |
FR2534493A1 (en) * | 1982-10-13 | 1984-04-20 | Elf Aquitaine | ENRICHMENT OF ORES BY FLOTATION AND COLLECTING AGENTS EMPLOYED THEREFOR |
FR2534492A1 (en) * | 1982-10-13 | 1984-04-20 | Elf Aquitaine | IMPROVEMENT IN MINERAL FLOTATION |
EP0107561A1 (en) * | 1982-10-13 | 1984-05-02 | Societe Nationale Elf Aquitaine (Production) | Flotation of ores |
EP0107562A1 (en) * | 1982-10-13 | 1984-05-02 | Societe Nationale Elf Aquitaine (Production) | Concentration of ores by flotation and collector reagents used therefor |
US4526696A (en) * | 1982-10-13 | 1985-07-02 | Societe Nationale Elf Aquitaine (Production) | Flotation of minerals |
WO1986006983A1 (en) * | 1985-05-31 | 1986-12-04 | The Dow Chemical Company | Novel collectors for the selective froth flotation of sulfide minerals |
US4735711A (en) * | 1985-05-31 | 1988-04-05 | The Dow Chemical Company | Novel collectors for the selective froth flotation of mineral sulfides |
AU576665B2 (en) * | 1985-05-31 | 1988-09-01 | Dow Chemical Company, The | Froth flotation of metal-containing sulphide minerals |
US4676890A (en) * | 1985-11-29 | 1987-06-30 | The Dow Chemical Company | Collector compositions for the froth flotation of mineral values |
US9512071B1 (en) | 2015-12-28 | 2016-12-06 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US9505011B1 (en) * | 2015-12-28 | 2016-11-29 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as mining chemical collectors |
US9512248B1 (en) | 2015-12-28 | 2016-12-06 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
US9631039B1 (en) | 2015-12-28 | 2017-04-25 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
US9738601B2 (en) | 2015-12-28 | 2017-08-22 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US9879102B2 (en) | 2015-12-28 | 2018-01-30 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
US9938237B2 (en) | 2015-12-28 | 2018-04-10 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US10000590B2 (en) | 2015-12-28 | 2018-06-19 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
US10011564B2 (en) | 2015-12-28 | 2018-07-03 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US10040758B2 (en) | 2015-12-28 | 2018-08-07 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and methods of making same |
US10294200B2 (en) | 2015-12-28 | 2019-05-21 | Chevron Phillips Chemical Company, Lp | Mixed branched eicosyl polysulfide compositions and methods of making same |
RU2715577C2 (en) * | 2015-12-28 | 2020-03-02 | ШЕВРОН ФИЛЛИПС КЕМИКАЛ КОМПАНИ ЭлПи | Compositions of mixed decylmercaptans and their use for extraction of chemical substances during extraction of minerals |
WO2018027046A1 (en) * | 2016-08-04 | 2018-02-08 | Chevron Phillips Chemical Company Lp | Mining collector compositions containing dodecylmethyl sulfide and processes for the recovery of metals therewith |
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