US1763851A - Concentration of ores - Google Patents
Concentration of ores Download PDFInfo
- Publication number
- US1763851A US1763851A US316366A US31636628A US1763851A US 1763851 A US1763851 A US 1763851A US 316366 A US316366 A US 316366A US 31636628 A US31636628 A US 31636628A US 1763851 A US1763851 A US 1763851A
- Authority
- US
- United States
- Prior art keywords
- flotation
- concentration
- ore
- tetrathio
- 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 description 11
- 238000005188 flotation Methods 0.000 description 7
- 150000002894 organic compounds Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- -1 tetraethyl tetrathio diphosphate Chemical compound 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000008396 flotation agent Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- IRDLUHRVLVEUHA-UHFFFAOYSA-N diethyl dithiophosphate Chemical compound CCOP(S)(=S)OCC IRDLUHRVLVEUHA-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 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 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000010269 sulphur dioxide Nutrition 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/014—Organic compounds containing phosphorus
-
- 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
- B03D2201/04—Frothers
-
- 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 the concentration of ores, minerals and the like by flotation, and has for its object the provision of certain improvements in flotation processes, and more particularly the froth flotation process.
- the present invention is based upon the discovery that tetrathio diphospho organic compounds are effective flotation agents. I have found that these compounds, in which two 0 molecules of an organic phosphorus and sulphur containing compound are made to combine into a single molecule, with two phoshorus atoms bonded through two intervenmg and linked sulphur atoms, have a marked selective action on the sulphide minerals as distinguished from gangue minerals; and when used in a flotation process, float the sulplhide minerals readily with an-attendant hig recovery of the metal values.
- the flotation agent which is typical of these tetrathio diphospho organic compounds may be conveniently made by addmg diethyl dithio phosphoric acid, or its metallic salt, during continuous stirring, to strong sulphuric acid, which must be cooled as soon as the reaction commences, to prevent decomposition.
- the reaction which continues for upwards of twenty minutes, accompanied by evolution of sulphur dioxide, may be represented as follows:
- the principal product of this reaction is a crystalline solid, of mild odor, which melts at 7 2-7 3 0., without decomposition or change in properties.
- R R 0 I Rao i s R10 i mo expresses what I believe to be the constitution so of the class of com ounds which I intend to claim for use in otation.
- R R R and B may represent any alkyl or aryl radicals or substituted derivatives thereof.
- the radicals maybe all alike, as in the tetraethyl compound described in detail above; or some, or all, may be different.
- Methyl, propyl, phenyl and "cresyl radicals may be mentioned, for example, as among those which can be represented by the s mbols R R R, and R above.
- phosphoric acids or their metallic salts
- any suit-able reagent that will effect the oxidation described.
- I may use any suitable oxidizing agent, such as sulphuric acid, the halogens, hypohaloids, chromic acid, dichromates or permanganates. Typical results obtained by adding these reagents to a mineral ore pulp and subjecting the resulting mixture to flotation are tabulated as follows:
Landscapes
- Paper (AREA)
Description
Patented June 17, 1930 PATENT OFFICE BENJAMIN I. JOHNSON, F GARFIELD, UTAH CONCENTRATION 013 031518 No Drawing.
This invention relates to the concentration of ores, minerals and the like by flotation, and has for its object the provision of certain improvements in flotation processes, and more particularly the froth flotation process.
The present invention is based upon the discovery that tetrathio diphospho organic compounds are effective flotation agents. I have found that these compounds, in which two 0 molecules of an organic phosphorus and sulphur containing compound are made to combine into a single molecule, with two phoshorus atoms bonded through two intervenmg and linked sulphur atoms, have a marked selective action on the sulphide minerals as distinguished from gangue minerals; and when used in a flotation process, float the sulplhide minerals readily with an-attendant hig recovery of the metal values.
I have also found that smaller amounts of these tetrathio diphospho organic compounds are needed to produce equivalent or better results in the flotation operation than other organic flotation agents heretofore generally used.
My investigations indicate that certain of the tetrathio diphospho organic compounds have insfiflicient frothing power to constitute a complete agent in froth-flotation, so that an appropriate frothing agent, such as pine oil, cresylic acid or the like, may be employed in conjunction therewith, in carrying out such froth-flotation operation.
The flotation agent which is typical of these tetrathio diphospho organic compounds may be conveniently made by addmg diethyl dithio phosphoric acid, or its metallic salt, during continuous stirring, to strong sulphuric acid, which must be cooled as soon as the reaction commences, to prevent decomposition. The reaction, which continues for upwards of twenty minutes, accompanied by evolution of sulphur dioxide, may be represented as follows:
2 c o rssn B so omlmmss-ssmomom so, 211.0
The principal product of this reaction is a crystalline solid, of mild odor, which melts at 7 2-7 3 0., without decomposition or change in properties.
Application filed October 31, i928. Serial No. mazes.
I propose to call this product tetraethyl tetrathio diphosphate, although other names may be equally appropriate. The following 1s a comparison of determined and theoretical constants of this product:
Determined Theoretinal Percent sulphur. 35. 4 Per cent phosphorus 16. 6 Molecular weight 369. 85
R 0 I Rao i s R10 i mo expresses what I believe to be the constitution so of the class of com ounds which I intend to claim for use in otation. In the general formula, R R R and B, may represent any alkyl or aryl radicals or substituted derivatives thereof. The radicals maybe all alike, as in the tetraethyl compound described in detail above; or some, or all, may be different. Methyl, propyl, phenyl and "cresyl radicals may be mentioned, for example, as among those which can be represented by the s mbols R R R, and R above. While'I believe that the above formula correctly represents the reaction product of an alkyl or aryl dithio phosphoric acid or its metal ic salt with an oxidizing a cut, it is understood that where I have used t is formula in the claims such reactionproduct is indicated thereby.
Generally, these tetrathio diphospho organic compounds may be prepared throu h the reaction of any of the organic di=th1o 1.00
phosphoric acids, or their metallic salts, with any suit-able reagent that will effect the oxidation described. I may use any suitable oxidizing agent, such as sulphuric acid, the halogens, hypohaloids, chromic acid, dichromates or permanganates. Typical results obtained by adding these reagents to a mineral ore pulp and subjecting the resulting mixture to flotation are tabulated as follows:
Utah Copper Company mill heading ground to a fine pulp and modified with burned lime and sodium cyanide was subjected to flotation in a J anney Laboratory machine. Gresylic acid was used at the rate of .3 ounds per ton of ore and tetraethyl tetrathio diphosphate used at the rate of .05 lbs. in Test 1 and at the rate of .025 lbs. in Test 2.
Heading Concentrate per cent Fe Rougher per cent Cu Rougher per cent Tailing per cent Fe Test Per cent Per cent Cu Fe I have found that these tetrathio diphospho organic compounds are effective flotation agents when mixed with a pulp so modified as to show either acid, alkaline or neutral reaction, and the resulting mixtures subjected to flotation operations.
I claim:
1. The improvement in the concentration of ore by froth flotation which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the resence of the reaction product of diethyl 'thio phosphoric acid with strong sulphuric acid.
2. The improvement in the concentration of ore by froth flotation which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of the reaction product of a metallic salt of diethyl dithio phosphoric acid with strong sulphuric acid.
3. The improvement in the concentration of ore by froth flotation which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of tetraethyl tetrathio diphosphate.
4. The improvement in the concentration of ore by froth flotation which comprises subjecting the ore in the form of a pulp to a froth flotation operation in the presence of a compound represented by the formula B40 in which R R R, and R stand for any alkyl or aryl organic radicals or substituted derivatives thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US316366A US1763851A (en) | 1928-10-31 | 1928-10-31 | Concentration of ores |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US316366A US1763851A (en) | 1928-10-31 | 1928-10-31 | Concentration of ores |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1763851A true US1763851A (en) | 1930-06-17 |
Family
ID=23228755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US316366A Expired - Lifetime US1763851A (en) | 1928-10-31 | 1928-10-31 | Concentration of ores |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1763851A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2471115A (en) * | 1946-09-19 | 1949-05-24 | Standard Oil Dev Co | Lubricating oil |
| US2983644A (en) * | 1955-08-18 | 1961-05-09 | Fmc Corp | Pesticidal compositions comprising phosphinothioyl disulfide |
-
1928
- 1928-10-31 US US316366A patent/US1763851A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2471115A (en) * | 1946-09-19 | 1949-05-24 | Standard Oil Dev Co | Lubricating oil |
| US2983644A (en) * | 1955-08-18 | 1961-05-09 | Fmc Corp | Pesticidal compositions comprising phosphinothioyl disulfide |
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