US1670021A - Treatment of copper minerals - Google Patents
Treatment of copper minerals Download PDFInfo
- Publication number
- US1670021A US1670021A US671392A US67139223A US1670021A US 1670021 A US1670021 A US 1670021A US 671392 A US671392 A US 671392A US 67139223 A US67139223 A US 67139223A US 1670021 A US1670021 A US 1670021A
- Authority
- US
- United States
- Prior art keywords
- copper
- pulp
- minerals
- flotation
- ore
- 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
- 229910001779 copper mineral Inorganic materials 0.000 title description 22
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 26
- 229910052802 copper Inorganic materials 0.000 description 26
- 239000010949 copper Substances 0.000 description 26
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 22
- 238000000576 coating method Methods 0.000 description 22
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 22
- 238000005188 flotation Methods 0.000 description 22
- 229910052500 inorganic mineral Inorganic materials 0.000 description 21
- 239000011707 mineral Substances 0.000 description 21
- 235000010755 mineral Nutrition 0.000 description 21
- 238000000034 method Methods 0.000 description 19
- 239000000243 solution Substances 0.000 description 13
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000000227 grinding Methods 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000001419 dependent effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- VWWMOACCGFHMEV-UHFFFAOYSA-N dicarbide(2-) Chemical compound [C-]#[C-] VWWMOACCGFHMEV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011790 ferrous sulphate Substances 0.000 description 3
- 235000003891 ferrous sulphate Nutrition 0.000 description 3
- 238000009291 froth flotation Methods 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000012476 oxidizable substance Substances 0.000 description 3
- 239000010665 pine oil Substances 0.000 description 3
- 238000009877 rendering Methods 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 241000779819 Syncarpia glomulifera Species 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 229940036248 turpentine Drugs 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000001293 FEMA 3089 Substances 0.000 description 1
- 235000006173 Larrea tridentata Nutrition 0.000 description 1
- 244000073231 Larrea tridentata Species 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229960002126 creosote Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052592 oxide mineral Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- B03D1/006—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
- 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 invention is a process for recovering with sulphur sometimes give poor recoveries when flotation is applied to them. This may be due to superficial oxidation, or to less understood causes connected with the nature of the minerals with which the sulphite is associated in the ore.
- the process to be described gives increased amenability to fiotation when applied to many copper minerals and particularly to those which are not adapted for flotation concentration by standard methods.
- Copper minerals in an ore may be so closely associated, either by chemical combination or physical proximity, with the minerals of other metals, that a process intended to make a copper mineral floatable may also aid in the flotation of the other,
- Copper minerals may be classified as cupric and cuprous depending on the state of oxidation of the element. Both these classes are amenable to the treatment herein described.
- cupric copper inalkaline, neutral or slightly acid solution in the presence of acet lene, becomes an oxidizing agent because 0 its tendency to precipitate as' a cuprous compound, cuprous acetylide.
- an oxidizable compound In order to produce this effect an oxidizable compound must also be present.
- This oxi dizable compound may be acetylene itself,
- slightly acid pulps may be desirable with some ores.
- Slig tly acid is here intended generally to express an acidity caused by the hydrolysis of a weak-base salt, e. g. ferrous sulphate. Free sulphuric acid might also be present in traces, but although it might help to attack the minerals, it might delay the required coating action andeventually might prevent it entirely. This is because the coating reaction itself makes acid by hydration and oxidation of the acetylene to acetic acid.
- alkaline pulps may be desirable.
- the alkalinity may be brought about by addition of lime or soda ash or caustic soda.
- this coating y the action of acetylene implies the injection and dissolution of the as in the liquid of the pul After suflic ent action has taken place t e excess gas may be removed from solution by heating the pulp or applying a vacuum.
- An ore may be ground with a. cold solution of lime, ammonia, pine oil, a flotation oiling oil and acetylene as. After grinding such a pulp mi t well be partially dehydrated or thickened to reso increase considerably the time available for the coating operation to reach a satisfactory condition. Such a thickened pulp would then be diluted with other water for the flotation operation.
- An ore may be ground with a warm solution of caustic soda, ammonia, glucose and a flotation oiling oil.
- the warm 1 to 1 pulp may be collected in a container and then acetylene gas injected so that the. whole is under pressure.
- the pulp should then be diluted with cold water and classified. Particles which had not been finely ground in the first instance would then come through again for further coating.
- An ore may be ground with a cold solution of ferrous sulphate, aniline, acetylene and a flotation oiling oil. Later in its progress such a pulp may, or not, be made alkaline, say with lime and the flotation operation carried out. The tail pulp from such an o erat-ion should be settled to recover valua le solution for reuse on fresh charges of ore.
- the flotation oils may be omitted or applied at other points in the scheme of operation.
- injection of the acetylene to form a solution of the gas in the pulp may be effected at any convenient point and by suitable means, as for example blowing the gas also carried N aOH, 1 pound per ton of ore,-
- Feed-2.10% total copper Feed2.00% oxide copper. Qoncentrate14.50% total copper. Concentrate-11.30% oxide copper. Tails0.7-7% total copper. Tails0.7 3% oxide copper.
- Coating act1on may be thus carried out over periods of days without reducing the tonnage capacity of the.
- the orcs contain minerals of other metals than copper, most commonly iron, lead and zinc, the treatment described has a selective action. It acts only on the particles of the copper minerals 'prcsent sothat in the subsequent flotation it is only, or mainlythe copper minerals which will be floated; so that the latter only will be selected and separated from other metals.
- any usual or suitable flotation oils and methods may be applied.
- the treatment may be used also to recover by flotation other elements which .may be closely associated with the copper minerals where the floatability of the particles is sufliciently great to'carry the percentage of the'other elements present in the particles.
- the ore contains mixed oxides and sulphides of coppe'r it may be subjected first to a flotation operation on the pulp to remove the sulphides of copper (or in fact any other minerals which are naturally floatable) after which the present process may be applied to the residue carrying oxides of copper or other diflicultly floatable copperto the particular embodiments described.
- a flotation operation on the pulp to remove the sulphides of copper (or in fact any other minerals which are naturally floatable) after which the present process may be applied to the residue carrying oxides of copper or other diflicultly floatable copperto the particular embodiments described.
- What claim is a 1.
- the method of treating ores containing copper minerals to increase their susceptibility to flotation concentration by processes dependent upon afiinity between minerals and a gaseous agent which consists in applying to 'apulpof the ores.
- acetylene and other oxidizable substances which results in insoluble substances thus producing on the particles of the said minores containing copper minerals to increase their susceptibility to subsequent flotation concentration by processes dependent upon afiinity between minerals and a gaseous agent.which consists in applying to a pulp of the ores acetylene gas under pressure
- the process which comprises rendering a pulp of copper ore alkaline; adding aniline; treating the pulp with acetylene until the floatability of the copper mineral is materially increased, and then floating the mineral, by froth flotation.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Patented May 15, 1928.
UNITED STATES PATENT OFFICE- IIOUIS F. CLARK, OF GRAND RAPIDS, MICHIGAN, ASSIGNOR TO UNION CARBIDE SALES COMPANY, OF NEW YORK, N. Y., A CORPORATION OF WEST VIRGINIA.
TREATMENT OF COPPER MINERALS.
No Drawing.
The invention is a process for recovering with sulphur sometimes give poor recoveries when flotation is applied to them. This may be due to superficial oxidation, or to less understood causes connected with the nature of the minerals with which the sulphite is associated in the ore. The process to be described gives increased amenability to fiotation when applied to many copper minerals and particularly to those which are not adapted for flotation concentration by standard methods.
Copper minerals in an ore may be so closely associated, either by chemical combination or physical proximity, with the minerals of other metals, that a process intended to make a copper mineral floatable may also aid in the flotation of the other,
minerals. But if such close association does not exist it is possible by a proper use of my' invention to select only the copper minerals in the ore and to separate them from the other minerals.
Copper minerals may be classified as cupric and cuprous depending on the state of oxidation of the element. Both these classes are amenable to the treatment herein described.
I have found that cupric copper inalkaline, neutral or slightly acid solution, in the presence of acet lene, becomes an oxidizing agent because 0 its tendency to precipitate as' a cuprous compound, cuprous acetylide. In order to produce this effect an oxidizable compound must also be present. This oxi dizable compound may be acetylene itself,
or some other oxidizable substance either organic or inorganic, for'example carbon monoxide or glucose. In some cases it is advantageous to use an oxidizable substance which can be converted into an insoluble Application filed October 29, 1923. Serial No. 671,892.
compound, such as a resin, by oxidation. Examples of this class of compounds are aniline, linseedoil, turpentine, and pine oil. Under suitable conditions the insoluble organic oxidation product is precipitated with the cuprous acetylide.
I have applied the above principle to the treatment of copper minerals, es ecially the oxide minerals, in an ore pulp. guch copper minerals, in a water pulp in' the presence of dissolved acetylene, are able to oxidize at.
their surface any oxidizable compound simultaneously dissolved. Thus a coating takes place on the surface of the copper mineral. primarily of the compound cuprous acetylide. If for example aniline, or turpentine, are also present dissolved in the water, then a composite coating is produced (a). The hydrogen ion concentration of the water used to make up the pulp, together with the influence of dissolved salts. This determines the extent to which the copper minerals may be superficially attacked so as to render them more amenable to the coating reaction and it also influences the ra idity of the coating reaction itself. T us,
slightly acid pulps may be desirable with some ores. Slig tly acid is here intended generally to express an acidity caused by the hydrolysis of a weak-base salt, e. g. ferrous sulphate. Free sulphuric acid might also be present in traces, but although it might help to attack the minerals, it might delay the required coating action andeventually might prevent it entirely. This is because the coating reaction itself makes acid by hydration and oxidation of the acetylene to acetic acid. On the 0 'her hand alkaline pulps may be desirable. The alkalinity may be brought about by addition of lime or soda ash or caustic soda. gaiimtly also addition of ammonia is help- These reagents tend to film the copper Fresilicates and other compounds with co per hydroxide which is itself especially a aptable to the coating reaction. Again, a combination of these conditions may be useful, as, for example, a treatment first with a weak solution of ferrous sulphate or sulphuric acid, followed by addition of alkali and the coating reagents. Also, the addition of other reagents may be useful for both purposes, e. g. sodium silicate, phosphate, chloride and so forth.
(b). The temperature of the solutions together with the concentration of the various substances dissolved 'are important. In general, especially if an alkaline pulp is used, a warm solution'is better than a cold one. Particularly it might be advantageous to heat an alkaline pulp during the operation of grinding so as to, increase the formation of hydroxide on the surfaces of the mineral particles. On the other hand, warming the ulp decreases the solubility of the most important element of the coating reagents, viz, the acetylene. Thus if a warmpulp is used it may be necessary to enclose it and inject acetylene gas under pressure.
' The time during which the reagents are allowed to act upon the mineral particles is also important. Both'the action of the surface attack on the mineral particles and the coating effect itself, are rather slow in operation. Warming the pulp seems to reduce'the time required.
. The preceding paragraphs have spoken perhaps too definitely of two phases of the procedure; first the attack on the surfaces of the mineral particles, and then the coating effect. In reality in operation it would be diflicult to say when one of these took place andthe other began or to tell their comparative extent. Similarly the whole coating result on one mineral might be quite different from that on another, and yet both give good flotation. In one case a coating very heavy and black might be required and in other an efiect not visible to the naked eye would be suflicient for satisfactory flotation. a
It should also be noted that this coating y the action of acetylene implies the injection and dissolution of the as in the liquid of the pul After suflic ent action has taken place t e excess gas may be removed from solution by heating the pulp or applying a vacuum.
' is process of coatin the copper mine erals in an ore pulp for iIotation concentration may in general. be applied with the regular machinery now in use for such ore dressing.
An ore may be ground with a. cold solution of lime, ammonia, pine oil, a flotation oiling oil and acetylene as. After grinding such a pulp mi t well be partially dehydrated or thickened to reso increase considerably the time available for the coating operation to reach a satisfactory condition. Such a thickened pulp would then be diluted with other water for the flotation operation.
An ore may be ground with a warm solution of caustic soda, ammonia, glucose and a flotation oiling oil. The warm 1 to 1 pulp may be collected in a container and then acetylene gas injected so that the. whole is under pressure. The pulp should then be diluted with cold water and classified. Particles which had not been finely ground in the first instance would then come through again for further coating.
An ore may be ground with a cold solution of ferrous sulphate, aniline, acetylene and a flotation oiling oil. Later in its progress such a pulp may, or not, be made alkaline, say with lime and the flotation operation carried out. The tail pulp from such an o erat-ion should be settled to recover valua le solution for reuse on fresh charges of ore.
' In any or all of these cases the flotation oils may be omitted or applied at other points in the scheme of operation. Likewise the injection of the acetylene to form a solution of the gas in the pulp may be effected at any convenient point and by suitable means, as for example blowing the gas also carried N aOH, 1 pound per ton of ore,-
and NH 0.80 pounds per ton. Temperature of pulp during grinding was 50 C. After grinding, the mixture was transferred to an autoclave using 1200 grams more of water as a wash, thus giving a 2 to 1 pulp. Now 1 pound more of N aOH per ton of ore and 0.80 pounds more of NH were added, together, with two pounds per ton of ore of aniline oil. Acetylene gas was now injected while the pulp was agitated and held at about 50 C. A pressure of about 25 pounds per square inch was maintained. At the end of about 15 minutes 'the coating eration was completed and the excess gas b own ofl. The pulp was now diluted with cold water to a 5 to 1 ratio and flotation conducted in a mechanically agitated machlne using coal tar, creosote and pine oil.
The following results were obtained;
Feed-2.10% total copper. Feed2.00% oxide copper. Qoncentrate14.50% total copper. Concentrate-11.30% oxide copper. Tails0.7-7% total copper. Tails0.7 3% oxide copper.
Recovery on total copper, 65.40 per cent. This example indicates what might be expected when comparatively large amounts of the reagents are applied in warm solution for a short time. 011 large scale work and where operation might be made continuous in such an apparatus as has been mentioned wherein the gas may be injected and recovered from the pulp as it passes through a pressure'container, more thorough coating may be expected and accordingly better flotation results.
In another example 1200 grams of 20- mesh ore were ground 30 minutes with 1200 ams of water which contained 0.80 pounds of NH and 1 pound of NaOH per ton of ore. A temperature of 50 C. was maintained during grinding. After grinding, the pulp was cooled to about 15 (J. and 1200 grams of cold water added. This last water carried aniline oil and acetylene dissolved amounting to 1 pound of each per ton of ore. The pulp was agitated and then allowed to stand in the liquid for 24 hours. It was then diluted and flotation carried out as before noted.' The following results were obtained.
Feed2.09% total copper.
2.00% oxide copper. Concentrate20.90% total copper. 18.70% oxide copper. -Tails0.79% total copper.
0.73% oxide copper.
Recovering on total copper, 62.00 per cent. This exam 1e illustrates the use of lesser amounts 0 reagentsin cold solution where the coating action was allowed to, proceed through considerable time. This indicates also the application before mentioned of a thickening device which would at once recover excess solution from the pulp and delay the advance of the solids until sufficient coating action had taken place.
This principle may be extended to a system of tank storage of thickened pulp containing smallamounts of the required reagents dissolved. Coating act1on may be thus carried out over periods of days without reducing the tonnage capacity of the.
milling plant. In such a case, however, and especially where an alkaline solution is used. the pulp' had best be protected as much as possible from sun light and air which would tend to cause consumption of acetylene by diiferencebetweenthe coating action of acetylene and of hydrogen sulphide. The latter coats indiscriminately iron, lead, copper and so forth and is thus largely consumed by Worthless minerals. I
\Vhere the orcs contain minerals of other metals than copper, most commonly iron, lead and zinc, the treatment described has a selective action. It acts only on the particles of the copper minerals 'prcsent sothat in the subsequent flotation it is only, or mainlythe copper minerals which will be floated; so that the latter only will be selected and separated from other metals.
For the flotation operation to which the treated ore is subsequently subjected, any usual or suitable flotation oils and methods may be applied. I The treatment may be used also to recover by flotation other elements which .may be closely associated with the copper minerals where the floatability of the particles is sufliciently great to'carry the percentage of the'other elements present in the particles.
WVhe-re the ore contains mixed oxides and sulphides of coppe'r it may be subjected first to a flotation operation on the pulp to remove the sulphides of copper (or in fact any other minerals which are naturally floatable) after which the present process may be applied to the residue carrying oxides of copper or other diflicultly floatable copperto the particular embodiments described. Various modifications in the steps of the process and in their'order and in the proportions ofthe ingredients stated may be made by those skilled in the artwithout de-. I parting'from the invention as defined in the followm claims.
What claim is a 1. The method of treating ores containing copper minerals to increase their susceptibility to flotation concentration by processes dependent upon afiinity between minerals and a gaseous agent which consists in applying to 'apulpof the ores. acetylene and other oxidizable substances, the oxidation of which results in insoluble substances thus producing on the particles of the said minores containing copper minerals to increase their susceptibility to subsequent flotation concentration by processes dependent upon afiinity between minerals and a gaseous agent.which consists in applying to a pulp of the ores acetylene gas under pressure,
the temperature of the pulp being too high to retain a substantial quantity of gas at atmospheric pressure.
4. The process which comprises treating a copper ore with acetylene until the floatability of the copper mineral is materially increased, and then floating the mineral, by froth flotation.
5. The process which comprises treating a pulp of copper ore with acetylene until the floatability of the copper mineral is materially increased, and then floating the mineral, by froth flotation. I
6. In a process of concentratin copper ores, the ste of treating a pulp the ore with acetylene until the floatability of the copper mineral by processes dependent upon affinity between minerals and a gaseous agent is materially in'creased..
7. The process which comprises rendering a pulp of copper ore alkaline; adding a nongaseous reducing agent; treating the pulp with acetylene until the fioatability of the copper mineral is materially increas'ed. and
then floating the mineral, by froth ,flotation.
8. The process which comprises rendering a pulp of copper ore alkaline; adding an organic reducing agent adapted to form a water-insoluble oxidation product; and treating the pulp with acetylene until the floatability of the copper mineral by processes dependent upon aflinity between minerals and a gaseous agent is materially increased. I
, 9. The process which comprises rendering a pulp of copper ore alkaline; adding aniline; treating the pulp with acetylene until the floatability of the copper mineral is materially increased, and then floating the mineral, by froth flotation.
In witness whereof, I have hereunto signed my name.
LOUIS F. CLARK.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US671392A US1670021A (en) | 1923-10-29 | 1923-10-29 | Treatment of copper minerals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US671392A US1670021A (en) | 1923-10-29 | 1923-10-29 | Treatment of copper minerals |
Publications (1)
Publication Number | Publication Date |
---|---|
US1670021A true US1670021A (en) | 1928-05-15 |
Family
ID=24694336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US671392A Expired - Lifetime US1670021A (en) | 1923-10-29 | 1923-10-29 | Treatment of copper minerals |
Country Status (1)
Country | Link |
---|---|
US (1) | US1670021A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2952532A (en) * | 1957-08-19 | 1960-09-13 | American Alcolac Corp | Beneficiation of ferruginous ores |
US3902602A (en) * | 1972-05-08 | 1975-09-02 | Vojislav Petrovich | Froth flotation method for recovery of minerals |
-
1923
- 1923-10-29 US US671392A patent/US1670021A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2952532A (en) * | 1957-08-19 | 1960-09-13 | American Alcolac Corp | Beneficiation of ferruginous ores |
US3902602A (en) * | 1972-05-08 | 1975-09-02 | Vojislav Petrovich | Froth flotation method for recovery of minerals |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US1670021A (en) | Treatment of copper minerals | |
US2957576A (en) | Recovery of molybdenite by flotation | |
US2839387A (en) | Method for the cyanidation of precious metals | |
US3130043A (en) | Recovery of nickel from laterite ores | |
US1801318A (en) | Concentration of ores | |
US4297108A (en) | Desulfurization of coal | |
US2556496A (en) | Purification of coal | |
US1636974A (en) | Selective flotation of minerals from crude ores | |
US1182890A (en) | Separation of metallic sulfids. | |
US1438436A (en) | Flotation process of concentrating sulphide ores | |
US2572519A (en) | Sweetening process | |
US1197589A (en) | Process of treating ores. | |
US3435952A (en) | Process and reagent for recovery of molybdenite from copper sulfide-molybdenite flotation concentrates | |
US1240598A (en) | Flotation of minerals. | |
US3400817A (en) | Process and reagent for recovery of molybdenite from copper sulfide-molybdenite flotation concentrates | |
US1628046A (en) | Ore flotation process | |
US1807860A (en) | Separation of minerals | |
US1240597A (en) | Flotation of minerals. | |
US1312668A (en) | Raymond f | |
US2085523A (en) | Sweetening process | |
US1523444A (en) | Process for the extraction of copper from its ores | |
US1236856A (en) | Ore concentration. | |
US1737717A (en) | Process for flotation of cassiterite | |
US1286532A (en) | Process of treating copper ores by sulfitization and flotation. | |
US1364858A (en) | Flotation of minerals |