US2690259A - Froth flotation of iron sulfide ore - Google Patents
Froth flotation of iron sulfide ore Download PDFInfo
- Publication number
- US2690259A US2690259A US256398A US25639851A US2690259A US 2690259 A US2690259 A US 2690259A US 256398 A US256398 A US 256398A US 25639851 A US25639851 A US 25639851A US 2690259 A US2690259 A US 2690259A
- Authority
- US
- United States
- Prior art keywords
- emulsion
- xanthate
- pulp
- ore
- flotation
- 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 claims description 12
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 title claims description 10
- 239000000839 emulsion Substances 0.000 claims description 43
- 239000012991 xanthate Substances 0.000 claims description 34
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 claims description 21
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 18
- -1 POLYOXYETHYLENE Polymers 0.000 claims description 15
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 14
- RZFBEFUNINJXRQ-UHFFFAOYSA-M sodium ethyl xanthate Chemical compound [Na+].CCOC([S-])=S RZFBEFUNINJXRQ-UHFFFAOYSA-M 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 9
- 230000005484 gravity Effects 0.000 claims description 8
- JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 claims description 7
- 238000004537 pulping Methods 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 claims description 5
- NZUFLKMNMAHESJ-UHFFFAOYSA-M potassium;propoxymethanedithioate Chemical compound [K+].CCCOC([S-])=S NZUFLKMNMAHESJ-UHFFFAOYSA-M 0.000 claims description 3
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical class [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 claims 1
- 238000005188 flotation Methods 0.000 description 21
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- 239000010665 pine oil Substances 0.000 description 13
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- 229910052742 iron Inorganic materials 0.000 description 9
- 239000012141 concentrate Substances 0.000 description 6
- 238000011084 recovery Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 5
- 239000011297 pine tar Substances 0.000 description 5
- 229940068124 pine tar Drugs 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- 235000006173 Larrea tridentata Nutrition 0.000 description 3
- 244000073231 Larrea tridentata Species 0.000 description 3
- DVRDHUBQLOKMHZ-UHFFFAOYSA-N chalcopyrite Chemical compound [S-2].[S-2].[Fe+2].[Cu+2] DVRDHUBQLOKMHZ-UHFFFAOYSA-N 0.000 description 3
- 229910052951 chalcopyrite Inorganic materials 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 150000004763 sulfides Chemical class 0.000 description 3
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 229910052976 metal sulfide Inorganic materials 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 2
- 229910052683 pyrite Inorganic materials 0.000 description 2
- 239000011028 pyrite Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000001794 pinus palustris tar oil Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000000126 substance 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
- B03D1/012—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
- 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
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/008—Organic compounds containing oxygen
-
- 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
- B03D2201/02—Collectors
-
- 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
Definitions
- This invention relates to the recoveryof metal sulfides by froth flotation, and'more particularly to the recovery of sulfides by the use of xanthate reagents in emulsified form.
- the principal object of this invention is the recovery of metal sulfides by means of an improved type of flotation reagent.
- Another object is to provide a flotation reagent composition which will recover iron pyrites more rapidly and more completely than has been possible heretofore.
- a further object is to retardthe decomposition of aqueous xanthate solutions by producing a xanthate emulsion.
- Iron pyrites or iron sulfide ores
- Iron pyrites are accompanied by considerable gangue material, and the most feasible means of separating the iron sulfide is by use of a froth flotation process.
- the magnetic iron oxide and chalcopyrite are first removed sequentially by well known means. After removal of the iron oxide and chalcopyrite, a pulp remains which contains largely iron pyrites and gangue.
- the pulp is subjected to a froth flotation process which usually comprises first, a treatment with copper sulfate solution to produce a clean, reactive, surface on the exposed particles of pyrites contained in the pulp.
- the pulp is subjected to predetermined amounts of a collector material, such as sodium ethyl xanthate, and a frother, such as pine oil.
- a collector material such as sodium ethyl xanthate
- a frother such as pine oil
- the collector and frother must be added separately. I have found that by combining the collector and frother in an emulsion, made with special emulsifying agents, not only is the addition ofthe flotation reagents made with greater facility, but also there is a considerable gain in flotation efiiciency. I;
- xanthate are dissolved in water to yield about 225gallons of solution.
- Another solution is made by dissolving 756 grams of polyoxyethylene lauryl alcohol in about two gallons of warm water.
- a quantity of from 10 to 30 gallons of xanthate solution is pumped thru a homogenizer, for example, a homogenizer of the Marco Flow-Master type, and the polyoxyethylene lauryl alcohol solution added to the xanthate slowly during the pumping operation.
- the solution thus produced is mixed with from 3 /2 to 15 gallons of G. N. S. No. 5 pine oil containing gallon of pine tar residue.
- the resultant solution is then pumped thru the homogenizer, set at a pressure of 250 to 700 p. s.
- the amount of polyoxyethylene lauryl alcohol used to make the emulsion should be held to any arbitrary limit.
- the amount of emulsifier needed to produce a satisfactory emulsion can best be determined by a simple series of tests to meet individual requirements.
- the type of polyoxyethylene lauryl alcohol useful in producing my emulsion is that form of the compound which has a specific gravity of from 1.18 to 1.22, and is a waxy appearing compound.
- any frother satisfactory in sulfide flotation which is symbiotic with the other ingredients in the emulsified state, may be used.
- Any of the products known as wood creosotes which result from the distillation of hard or soft woods, will operate as satisfactory frothers in my flotation emulsion.
- wood creosotes mean to include any of the oily components found in either the distillate or the tarry fractions in the residue after distillation. Typical examples of wood creosotes are, pine oil, pine tar and pine tar oil.
- Collectors which may be used in forming the emulsion are sodium ethyl xanthate, sodium propyl xanthate, potassium ethyl xanthate and potassium propyl xanthate. I have found that enhanced recovery of concentrate is obtained when using an emulsion made up with a mixture of sodium ethyl xanthate and potassium ethyl xanthate, preferably in the ratio of 1 to 1, over the results obtained when only a single xanthate is'used in the emulsion.
- frother may be added to the pulp in the manner previously described, and separate additions of frother are then made as required.
- frother may be of any substance normally used as a frothing agent in the separation of sulfide ores.
- EXAMPLE I A portion of iron pyrites pulp, resulting from extraction from a magnetite ore, to which copper sulfate had been added, was treated with an emulsion of sodium ethyl xanthate,. pine oil and polyoxyethylene lauryl alcohol in proportions equivalent to 0.15 pound of xanthate and 0.02 pound of pine oil, per ton of feed, in a laboratory size flotation machine. The froth was removed by skimming for a total of 2 /4: minutes. It was filtered, dried, weighed and analyzed. for sulfur. A comparative test fusing a similar pulp was run wherein the xanthate and pine oil were added separately in the same equivalent amounts. The results of these two tests are presented as follows:
- the mixed xanthate emulsions were used in the pyrite flotation plant for four days direct- 1y following the test with the sodium ethyl xanthate emulsion.
- the results of this plant test work are presented in the following tables.
- a method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22) a collector of the group consisting of sodium ethyl xanthate, sodium propyl xanthate, potassium ethyl xanthate, potassium propyl xanthate and mixtures thereof, and a wood cerosote frother, and subjecting the pulp to a froth flotation operation.
- polyoxyethylene lauryl alcohol specifically gravity 1.18-1.22
- a method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), sodium ethyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
- a method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), a mixture (1 to 1) of sodium ethyl xanthate and potassium ethyl xanthate, and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
- a method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), sodium propyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
- a method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), potassium ethyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
- a method of concentrating iron sulfideore which comprises pulping the ore adding to the pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22) sodium ethyl xanthate and pine oil, and subjecting the pulp to a froth flotation operation.
Landscapes
- Paper (AREA)
Description
Patented Sept. 28, 1954 FROTH FLOTATION OF IRON SULFIDE ORE Arvid Emil Anderson, Cornwall, Pa., assignor to Bethlehem Steel Company, a corporation of Pennsylvania No Drawing. Application November 14, 1951, Serial No. 256,398
1 This invention relates to the recoveryof metal sulfides by froth flotation, and'more particularly to the recovery of sulfides by the use of xanthate reagents in emulsified form.
The principal object of this invention is the recovery of metal sulfides by means of an improved type of flotation reagent.
Another object is to provide a flotation reagent composition which will recover iron pyrites more rapidly and more completely than has been possible heretofore.
A further object is to retardthe decomposition of aqueous xanthate solutions by producing a xanthate emulsion.
Iron pyrites, or iron sulfide ores, are accompanied by considerable gangue material, and the most feasible means of separating the iron sulfide is by use of a froth flotation process. In certain types of magnetite ores, which also contain economically recoverable quantities of chalcopyrite and iron pyrites, the magnetic iron oxide and chalcopyrite are first removed sequentially by well known means. After removal of the iron oxide and chalcopyrite, a pulp remains which contains largely iron pyrites and gangue. To remove the iron pyrites in relatively pure form from the pulp, and thus free it from gangue and any metal values contained therein, the pulp is subjected to a froth flotation process which usually comprises first, a treatment with copper sulfate solution to produce a clean, reactive, surface on the exposed particles of pyrites contained in the pulp.
Secondly, the pulp is subjected to predetermined amounts of a collector material, such as sodium ethyl xanthate, and a frother, such as pine oil.
In this manner, commercially useful iron pyrites can be obtained.
In the method just described, the collector and frother must be added separately. I have found that by combining the collector and frother in an emulsion, made with special emulsifying agents, not only is the addition ofthe flotation reagents made with greater facility, but also there is a considerable gain in flotation efiiciency. I;
have found that this increased flotation efficiency is obtained by emulsifying the alcohol xanthates and a irother material, such as, pine oil with waxy polyoxyethylene lauryl alcohol, and adding the emulsion so made directly to the flotation pulp. By use of my improved reagent emulsion, in place of the reagents being added separately, I have been able to obtain a definite increase in recovery of concentrate.
In order to produce a quantity of my emulsion which will yield an adequate supply'and be convenient to handle, 250 pounds of sodium ethyl xanthate and 250 pounds of potassium ethyl 6 Claims. (Cl. 209166) oilto 1.
xanthate are dissolved in water to yield about 225gallons of solution. Another solution is made by dissolving 756 grams of polyoxyethylene lauryl alcohol in about two gallons of warm water. A quantity of from 10 to 30 gallons of xanthate solution is pumped thru a homogenizer, for example, a homogenizer of the Marco Flow-Master type, and the polyoxyethylene lauryl alcohol solution added to the xanthate slowly during the pumping operation. The solution thus produced is mixed with from 3 /2 to 15 gallons of G. N. S. No. 5 pine oil containing gallon of pine tar residue. The resultant solution is then pumped thru the homogenizer, set at a pressure of 250 to 700 p. s. 1., until a good emulsion is made and this emulsion is then dispersed thru the remainder of the xanthate solution by pumping the total solution thru the homogenizer. In this manner a stable emulsion can be produced which will retain its collector properties when added to large quantities of pulp in the flotation machines.
It should be noted that while the amounts given in the foregoing description for the preparation of the emulsion have proved quite satisfactory, it is notrequired that the proportions given be rigidly adhered to. Considerable variation of the proportions of ingredients is permissible, the desideratum being, of course, selection of quantities of reagent and emulsifier which will form a stable and acceptable emulsified xanthate flotation reagent under the particular conditions in which it may be used. Illustrative of the variation of quantities permitted in the production of the emulsified reagent is the case of pine oil. As has been mentioned, pine oil may be added, in the example given, in quantities ranging from 3 to 15 gallons, for the amount of pine oil needed will vary with the operating requirements. Likewise, it is not intended that the amount of polyoxyethylene lauryl alcohol used to make the emulsion should be held to any arbitrary limit. The amount of emulsifier needed to produce a satisfactory emulsion can best be determined by a simple series of tests to meet individual requirements.
In the preceding example, it is to be noted that a mixture of, sodium ethyl xanthate and potassium ethyl xanthate has been used in the ratio given, has proved to be the most efficient, excellent results can be obtained with difierent proportions of the two xanthates than the one given. Moreover, it is not necessary to use a mixture of potassium and sodium ethyl xanthates, for either one of the xanthates used alone in an 3 amount of 500 pounds (for the example shown) will prove satisfactory.
While the mixture, at the specific ratio The type of polyoxyethylene lauryl alcohol useful in producing my emulsion is that form of the compound which has a specific gravity of from 1.18 to 1.22, and is a waxy appearing compound.
While so far I have mentioned only pine oil and pine tar residue as the frothing ingredient, any frother satisfactory in sulfide flotation, which is symbiotic with the other ingredients in the emulsified state, may be used. Any of the products known as wood creosotes, which result from the distillation of hard or soft woods, will operate as satisfactory frothers in my flotation emulsion. By wood creosotes I mean to include any of the oily components found in either the distillate or the tarry fractions in the residue after distillation. Typical examples of wood creosotes are, pine oil, pine tar and pine tar oil.
Collectors which may be used in forming the emulsion are sodium ethyl xanthate, sodium propyl xanthate, potassium ethyl xanthate and potassium propyl xanthate. I have found that enhanced recovery of concentrate is obtained when using an emulsion made up with a mixture of sodium ethyl xanthate and potassium ethyl xanthate, preferably in the ratio of 1 to 1, over the results obtained when only a single xanthate is'used in the emulsion.
It is well known to use xanthates of some of the higher alcohols as collectors in flotation processes, and while the added cost of such higher alcohol xanthates makes them less to be preferred than the xanthates already mentioned, it is intended that the higher alcohol xanthates, which are operable as collectors with iron. sulflde ores and are amenable to emulsification, should come within the spirit of my invention. Of the higher alcohol xanthates, the butyl and amyl xanthates, especially, are effective in my emulsion. The higher alcohol xanthates are particularly useful in the treatment of arsenopyrites, as well as in treating copper and lead sulfides.
When treating sulfide ores, or pulps, a knowledge of the nature of the ore to be treated is of course necessary in order to obtain the most efficient separation in the flotation process. Keeping this fact in mind, a satisfactory reagent emulsion can be prepared for any kind and condition of sulfide ore. In performing the actual flotation separation, pulp is introduced into the flotation machine in the usual manner and flotation reagent emulsion is added to the pulp slowly. The amount of emulsion added may range from an equivalent of 0.1 pound to 0.5 pound of xanthate per ton of dry ore treated.
I have found that changes in temperature of the pulp, when using the emulsion, do not affect the flotation of the sulfides as markedly as when the xanthate and pine oil are added separately.
Depending on the nature of the ore, and the particular conditions under which the flotation is performed, it may in some cases be desirable to add additional frother to the system. When additional frother is added, the pulp is subjected to my flotation emulsion in the manner previously described, and separate additions of frother are then made as required. When frother is added separately, and in addition to that frother material already in the emulsion, the additional frother may be of any substance normally used as a frothing agent in the separation of sulfide ores.
The following examples indicate results for the recovery of concentrates obtained when using my emulsion as against results when using reagents in non-emulsified form, as well as results from the use of mixed xanthate emulsion and single xanthate emulsion.
EXAMPLE I A portion of iron pyrites pulp, resulting from extraction from a magnetite ore, to which copper sulfate had been added, was treated with an emulsion of sodium ethyl xanthate,. pine oil and polyoxyethylene lauryl alcohol in proportions equivalent to 0.15 pound of xanthate and 0.02 pound of pine oil, per ton of feed, in a laboratory size flotation machine. The froth was removed by skimming for a total of 2 /4: minutes. It was filtered, dried, weighed and analyzed. for sulfur. A comparative test fusing a similar pulp was run wherein the xanthate and pine oil were added separately in the same equivalent amounts. The results of these two tests are presented as follows:
Polyomyethylene lauryl alcohol emulsion The foregoing example indicates a considerable gain in recovery of concentrate when emulsion is used, and this gain is believed to be attributable to the fact that the emulsion enhances the stability of the xanthate, and develops a more nearly complete dispersion of the collector and frother than can possibly be attained when collector and frother are added separately.
In the tables, sulfide ore, in the respective feed, tailing and concentrate, is recorded as yield of sulfur (S) EXAMPLE II A sodium ethyl xanthate, pine oil-pine tar residue, polyoxytheylene lauryl alcohol emulsion was prepared and used in a pyrite flotation plant for four consecutive days. In a similar manner, a mixture of equal parts of sodium and potassium 1 ethyl xanthates were made into a pine oil-pine tar residue, polyoxyethylene lauryl alcohol emulsion. The mixed xanthate emulsions were used in the pyrite flotation plant for four days direct- 1y following the test with the sodium ethyl xanthate emulsion. The results of this plant test work are presented in the following tables.
Polyozcyethylene lauryl alcohol emulsion with single wanthate Polyomyethylene lauryl alcohol emulsion with mixed xanthates Percent Product by Pergent Yled of weight Concentrate 6. 37 51. 40 77. 0 Tailing 93. 63 1. 04 23.0 Feed 100 4. 25 100 I claim:
1. A method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22) a collector of the group consisting of sodium ethyl xanthate, sodium propyl xanthate, potassium ethyl xanthate, potassium propyl xanthate and mixtures thereof, and a wood cerosote frother, and subjecting the pulp to a froth flotation operation.
2. A method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), sodium ethyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
3. A method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), a mixture (1 to 1) of sodium ethyl xanthate and potassium ethyl xanthate, and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
4. A method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), sodium propyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
S. A method of concentrating iron sulfide ore which comprises pulping the ore adding to the ore pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22), potassium ethyl xanthate and a wood creosote frother, and subjecting the pulp to a froth flotation operation.
6. A method of concentrating iron sulfideore which comprises pulping the ore adding to the pulp an emulsion comprising polyoxyethylene lauryl alcohol (specific gravity 1.18-1.22) sodium ethyl xanthate and pine oil, and subjecting the pulp to a froth flotation operation.
References Cited in the file of this patent UNITED STATES PATENTS Name Date Schoeller et a1 Aug. 21, 1934 OTHER REFERENCES Number
Claims (1)
1. A METHOD OF CONCENTRATING IRON SULFIDE ORE WHICH COMPRISES PULPING THE ORE ADDING TO THE ORE PULP AN EMULSION COMPRISING POLYOXYETHYLENE LAURYL ALCOHOL (SPECIFIC GRAVITY 1.18-1.22), A COLLECTOR OF THE GROUP CONSISTING OF SODIUM ETHYL XANTHATE, SODIUM PROPYL XANTHATE, POTASSIUM ETHYL XANTHATE, POTASSIUM PROPYL XANTHATE AND MIXTURES THEREOF, AND A WOOD CREOSOTE FROTHER, AND SUBJECTING THE PULP TO A FROTH FLOTATION OPERATION.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US256398A US2690259A (en) | 1951-11-14 | 1951-11-14 | Froth flotation of iron sulfide ore |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US256398A US2690259A (en) | 1951-11-14 | 1951-11-14 | Froth flotation of iron sulfide ore |
Publications (1)
Publication Number | Publication Date |
---|---|
US2690259A true US2690259A (en) | 1954-09-28 |
Family
ID=22972102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US256398A Expired - Lifetime US2690259A (en) | 1951-11-14 | 1951-11-14 | Froth flotation of iron sulfide ore |
Country Status (1)
Country | Link |
---|---|
US (1) | US2690259A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2950818A (en) * | 1955-03-05 | 1960-08-30 | Hoechst Ag | Flotation process |
FR2534492A1 (en) * | 1982-10-13 | 1984-04-20 | Elf Aquitaine | IMPROVEMENT IN MINERAL FLOTATION |
US4678562A (en) * | 1982-10-14 | 1987-07-07 | Sherex Chemical Company, Inc. | Promotors for froth floatation of coal |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries |
-
1951
- 1951-11-14 US US256398A patent/US2690259A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2950818A (en) * | 1955-03-05 | 1960-08-30 | Hoechst Ag | Flotation process |
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 |
US4678562A (en) * | 1982-10-14 | 1987-07-07 | Sherex Chemical Company, Inc. | Promotors for froth floatation of coal |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2748938A (en) | Flotation of spodumene | |
US2342277A (en) | Separation of pyrite, arsenopyrite, and pyrrhotite by flotation | |
US2070076A (en) | Separation of molybdenite from copper sulphides | |
US2690259A (en) | Froth flotation of iron sulfide ore | |
US4196092A (en) | Conditioning agent for froth flotation of fine coal | |
US2065053A (en) | Flotation frother | |
US2676705A (en) | Concentration of phosphate ores | |
US2011176A (en) | Ore concentration | |
US1912433A (en) | Mineral concentration | |
US1773997A (en) | Process for the extraction of resin from coal | |
US4814070A (en) | Alkyl sulfosuccinates based on alkoxylated fatty alcohols as collectors for non-sulfidic ores | |
US2335485A (en) | Flotation of cement minerals | |
US4199065A (en) | Process for recovery of fine coal | |
US1697402A (en) | Concentration of sulphur | |
US2469422A (en) | Selective flotation of chromite ores | |
US2364272A (en) | Mineral concentration | |
US3182798A (en) | Process of recovering cassiterite from ores | |
US2084413A (en) | Flotation reagent | |
US1761546A (en) | Concentration of phosphate-bearing material | |
US2467369A (en) | Froth flotation of ores with aromatic alcohol | |
US2636604A (en) | Flotation of pyrites from a pyrite ore pulp | |
US1636974A (en) | Selective flotation of minerals from crude ores | |
CA1111155A (en) | Ore beneficiation | |
US2287274A (en) | Process of separating lead and zinc sulphides | |
US1668917A (en) | Froth-flotation concentration of ores |