US2286374A - Flotation process - Google Patents
Flotation process Download PDFInfo
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- US2286374A US2286374A US304707A US30470739A US2286374A US 2286374 A US2286374 A US 2286374A US 304707 A US304707 A US 304707A US 30470739 A US30470739 A US 30470739A US 2286374 A US2286374 A US 2286374A
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- United States
- Prior art keywords
- oil
- sulfonated
- pine
- pine oil
- frothing
- 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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- 238000000034 method Methods 0.000 title description 18
- 238000005188 flotation Methods 0.000 title description 12
- 239000010665 pine oil Substances 0.000 description 29
- 238000009291 froth flotation Methods 0.000 description 17
- 239000004359 castor oil Substances 0.000 description 16
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- 150000002430 hydrocarbons Chemical class 0.000 description 12
- 238000011084 recovery Methods 0.000 description 11
- 239000002184 metal Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 9
- 229910052500 inorganic mineral Inorganic materials 0.000 description 9
- 239000003350 kerosene Substances 0.000 description 9
- 239000011707 mineral Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 8
- 235000011613 Pinus brutia Nutrition 0.000 description 8
- 241000018646 Pinus brutia Species 0.000 description 8
- 239000007900 aqueous suspension Substances 0.000 description 8
- 235000019438 castor oil Nutrition 0.000 description 8
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 8
- -1 aliphatic alcohols Chemical class 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 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 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- WSKGRAGZAQRSED-SLFFLAALSA-N dehydroabietadienol Chemical compound OC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 WSKGRAGZAQRSED-SLFFLAALSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- YWJHQHJWHJRTAB-UHFFFAOYSA-N 4-(2-Methoxypropan-2-yl)-1-methylcyclohex-1-ene Chemical compound COC(C)(C)C1CCC(C)=CC1 YWJHQHJWHJRTAB-UHFFFAOYSA-N 0.000 description 2
- 101100005297 Mus musculus Cat gene Proteins 0.000 description 2
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000008396 flotation agent Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 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
- 244000126822 Albuca minor Species 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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil 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
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- 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 froth flotation processes and more particularly to froth flotation processes for separating metallic minerals wherein a blended pine oil or pine oil derivative is utilized as a frothing agent.
- An object of the present invention is to overcome the foregoing difficulties.
- Another object is to improve froth flotation processes andincrease the recovery of metals or minerals.
- a further object is to utilize frothingagents under conditions to produce a maximum concentration and a more efficient separation of the minerals and metals. 7
- the blend may be cut with suitable hydrocarbons and may beused in conjunction with suitable flotation agents.
- the blend comprises equal volumes of pine oil or the like and hydrocarbons mixed with about 10% of an emulsifying agent, although good results may be attained with other proportions of materials as will be pointed out hereafter.
- pine oil or the like suitably blended, can be any pine oil or the like, suitably blended.
- pine oil is referred to herein and in the appended claims, I mean pine oil of the commercial grade, synthetic pine oil, and pine oilde'rivatives prepared by air oxidation of terpene hydrocarbons and containing alcohols,
- ethers such as terpinyl methyl ether or air oxidized acyclic terpene hydrocarbons.
- pinene-phenol condensate s'ulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters, such as sulfonated castor oil, or a compound (sold under the trade name of Hercota) which is made by heating ethanolamine or triethanolamine and vegetable oils, such as castor oil.
- pine oil-emulsifying agent-hydrocarbon blendjI may use aliphatic or aromatic hydrocarbons, or mixtures thereof 1 have found that v hydrocarbons having a boiling range between C. and 300 C., but preferably between 150 toluol'). The boiling ranges of these hydrocan;
- Solvesso No. 2 '134' to C Solvesso No. 3 185 to 215 C.
- Solvesso No. 4 215 to 282 C.
- 01' will be indicated in the 55 Kero ene 183 to 255 C,
- the froth flotation reagents that is, the pine .oil blends, may comprise pine oil and from 1 to 25%, but preferably from to emulsifier, and hydrocarbons in any desired proportions, 'although mixturesof equalvolumes' of pine oil and hydrocarbon are-fpreferred.
- the metallic type are froth floated,-small amounts of I salts such as sodium cyanide or a thiophosphoric acid containing 6% thiocarbanilide (Aerofloat N0. 31) or other materials as indicated hereafter, may be utilized to assist in increasing the eifectiveness or the frothing. reagents.
- I salts such as sodium cyanide or a thiophosphoric acid containing 6% thiocarbanilide (Aerofloat N0. 31) or other materials as indicated hereafter, may be utilized to assist in increasing the eifectiveness or the frothing. reagents.
- the ore or mineralLto be dressed, concentrated, or classified is first ground to a pulverized or finely divided state and is fed to a flotation tank of any well-known design which contains water.
- Example I A volume of a-lead ore flotation pulp, correto a 2000 g. flotation cell. Then 0.008flb. of sodiumcyanide per ton of ore, 0.06lb. of Aerofloat No. '31 (a thiophosphoric acid +-6% thiocarbanilide) and the frother as listed below, were added.
- Example IV One thousand ten (1010) gfof St. .loseph Lead Company's Bonne Terre, Missouri, minus8 mesh ,lead ore were ground-in a ball mill for 12 minutes with 1000 cc. of distilled water. The ground ore'was screened through a 65 mesh screen'and .pulp were added the following fiothers, but no other reagents. The tests were carried out for 20 minutes.
- v P d P t Pb can a ercen Percent Pb Frother per in concenton mm f P 90% of equal volume of pine' 'oil and kerosene+l0% Herwta. 0. 20 68. 88 80. 3 00% of above blend- ⁇ 40% sulionated water oil 0. 20 68. 70 76. 6- 90% pine oll+l0% suliouated castor oil .L 0. 20 43. 73 76. 3
- Example VI low, were added. Air was passed through the pulp and a concentrate was taken on for 20
- Example VII About 830 g. of minus 8 mesh Matahambrecopper ore from Santa Lucia, Cuba, were ground in a ball mill for 14 minutes with 1000 cc.- of distilled water. The ground ore, was screened through a 48-mesh screen and then transferred to a 1000 g. flotation cell and further diluted to about 16% solids. 111 addition to the frother, the following materials were added to the pulp: Sodium cyanide lb. per ton of ore 0.10 Lime a [on 1.20 Potassium ethyl xanthate do 0.18
- Example VIII ores of the metal bearing type.
- the pine oil blends utilized in carrying .out the process provide a relatively high recovery. Relatively small amounts of the blends are effective to separate the metals from the gangue in an expedient manner, thereby decreasing the cost of the frothing reagents and increasing the plant capacity.
- a process for the froth flotation of sulfide ores which comprises frothing an aqueous susing agent comprising major proportions of pine About 1030 g. of the same Matahambre copper ore were ground in a ballmill for 14 minutes with 1000 cc. of distilled water. The ground ore was screened througha 48-mesh screenand then transferred to a 1000 g. flotation cell and further diluted to about20% solids.
- the following-materials were added:
- the present invention provides an improved froth flotation process for separating, collecting, or classifying minerals or oil and a hydrocarbon compound and .a minor proportion of an emulsifying agent selected from the group consisting of sulfonated pinene-cresol condensate, sulfonated pinene-phenol condensate, sulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters, ethanolamine-castor oil- -condensates and triethanolamine-castor oil condensates. 2.
- an emulsifying agent selected from the group consisting of sulfonated pinene-cresol condensate, sulfonated pinene-phenol condensate, sulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters, ethanolamine-castor oil- -condensates and triethanolamine-castor oil condensates.
- a processfor the froth flotation of sulfide ores which comprises frothing an aqueous suspension of' said ores in the presence of a frothing agent comprising major proportions of pine oil and a hydrocarbon compound and a minor proportion of an ethanolamine-castor oil condensate.
- ores which comprises frothing an aqueous suspension of .said ores in the presence of a frothing agent comprising major proportions of pineoil and a hydrocarbon compound and a minor proportion of a triethanolamine-castor oil condensate.
- a process for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said ores in the presence of a frothing agent comprising major proportions of pine oil 7 and a hydrocarbon-compound having a boiling range between about 100 C. and about 300 C. and a minor proportion of an emulsifyingagent selected from the group consisting of sulfonated pinene-cresol condensate, sulfonated pinenephenol condensate, sulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters,
- A- process for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said ores in. the presence of 'a frothing agent comprising major proportions of pine oil and a hydrocarbon compound and from about 1 to about 25% of an emulsifying agent selected from the group consisting ofsulfonated pinenecresol condensate, sulfonated pinene phenol condensate. sulfated dehydroabietyl alcohol, sulfonated higher fatty acid .esters, ethanolaminecastor oil condensates and triethanolaminecastor oil condensates.
- dehydroabietyl alcohol dehydroabietyl alcohol, sulfonated higher fatty acid esters, ethanolamine castor oil condensates and triethanolamine-castor oil condensates.
- a process for the froth flotation of sulfide ores whichcomprises frothing an aqueous suspension of said ores in-the presence of a frothing agent comprising major proportions of terpinyl methyl ether and kerosene and a. minor. 5 .proportion of. an ethanolamine-castor oil.condensate. r
- a proeess for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said oresin the presence of a irothi'ng m agent comprising substantially equal volumes of a commercial pine oil-and kerosene and about 10% of an ethanolamine-castor oil condensate.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Patented June 16, 1942" FLOTATIONTROCESS lfhilip A. Ray, Wilmington, Del., assignor to Hercules Powder Company, Wilmington, DeL,
a corporation of Delaware No Drawing. Application November 16, 1939, Serial N0. 304,707
9 Claims. 01. 200-166) This invention relates .to froth flotation processes and more particularly to froth flotation processes for separating metallic minerals wherein a blended pine oil or pine oil derivative is utilized as a frothing agent.
In the separation of metals from metal-bearing minerals or ores by froth flotation processes,
the percentage of recoveryof the metals is,
; largely due to the character of the frothing reagents employed. Nowadays it is desirable to get a very high recovery of metals in a very rapid and most efiicient manner. For example, today a recovery under 80%, in most cases is' 'considered poor, while years ago, a recovery of 60% was considered good. With the increase in efficiency of flotation processes, competition has become extremely keen and the successful operation of ore dressing or metallurgical plants may depend upon an increase in the recovery of metal of only a few percent. This is particularly soif the mineral or ore to (be dressed is of the low metal bearing quality or the plant operates on a small margin of profit.
Heretofore fatty acids, soaps, sulfonated. products, pine oil, cresylic acid, and special aliphatic alcohols have been utilized as frothing reagents.
, The first three mentioned frequently were quite unsatisfactory because the desired selectivity could not be obtained and more particularly because the gangue would float in large concentrations. An excessive amount'of reagents was often required to get a good recovery. This presented a serious economical problem, particularly when pine oil was used as a frother. Pine oil at times was not readily available on the market because the demand was greater than the supply and the prices thereof increased to an extent which made its use prohibitive.
An object of the present invention is to overcome the foregoing difficulties.
Another object is to improve froth flotation processes andincrease the recovery of metals or minerals. v
Another objectis to decrease the cost of froth flotation processes by utilizing frothing reagents appended claims, and various advantages not referred toherein will occur to one skilled in which are inexpensive, are readily available on the market at all times, and need not be-used in large quantities.
A further object is to utilize frothingagents under conditions to produce a maximum concentration and a more efficient separation of the minerals and metals. 7
Other and further objects will be obvious upon an understanding of the illustrative embodiment the art .upon employment of the invention in practice.
These objects are accomplished by frothing an .aqueous suspension of minerals .or ores in the presence of a blended pine oil or pine oil derivative'acting as a frother and containing an emulsifying agent and a hydrocarbon. In addition, if desired, the blend may be cut with suitable hydrocarbons and may beused in conjunction with suitable flotation agents. Preferably, the blend comprises equal volumes of pine oil or the like and hydrocarbons mixed with about 10% of an emulsifying agent, although good results may be attained with other proportions of materials as will be pointed out hereafter.
In accordance with the invention, I have found that pine oil or the like, suitably blended, can
be used advantageously as a froth flotation agent. When pine oil is referred to herein and in the appended claims, I mean pine oil of the commercial grade, synthetic pine oil, and pine oilde'rivatives prepared by air oxidation of terpene hydrocarbons and containing alcohols,
ethers, oxides, etc., such as terpinyl methyl ether or air oxidized acyclic terpene hydrocarbons.
I prefer to blend the pine oil and hydrocarbons with an emulsifying agent which may be sulfonated pinene-cresol condensate, sulfonated,
pinene-phenol condensate, s'ulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters, such as sulfonated castor oil, or a compound (sold under the trade name of Hercota) which is made by heating ethanolamine or triethanolamine and vegetable oils, such as castor oil.
In the pine oil-emulsifying agent-hydrocarbon blendjI may use aliphatic or aromatic hydrocarbons, or mixtures thereof 1 have found that v hydrocarbons having a boiling range between C. and 300 C., but preferably between 150 toluol'). The boiling ranges of these hydrocan;
bons are as follows:' Troluoil to C.
Solvesso No. 2 '134' to C. Solvesso No. 3 185 to 215 C. Solvesso No. 4 215 to 282 C.
about to be described, 01' will be indicated in the 55 Kero ene 183 to 255 C,
. sponding to about 2500 g. of ore, was transferred trate' was taken'off. for 20 inutes.
The froth flotation reagents, that is, the pine .oil blends, may comprise pine oil and from 1 to 25%, but preferably from to emulsifier, and hydrocarbons in any desired proportions, 'although mixturesof equalvolumes' of pine oil and hydrocarbon are-fpreferred. The reagents, preferablyf are prepared them-'i prior .to add-= I {ing them to ;the' flotation tank tdjassure thorough admixture)- or the ingredien to i facilitate controlling.- ltheconcentration ereofin the course or flotation procesaybut may be added individually to the tank, if so desired. In practice, where minerals: or ores, particularly of. the metallic type are froth floated,-small amounts of I salts such as sodium cyanide or a thiophosphoric acid containing 6% thiocarbanilide (Aerofloat N0. 31) or other materials as indicated hereafter, may be utilized to assist in increasing the eifectiveness or the frothing. reagents.
In carrying out the froth flotation process, the ore or mineralLto be dressed, concentrated, or classified is first ground to a pulverized or finely divided state and is fed to a flotation tank of any well-known design which contains water. The
minerals andwater are mechanically agitated 5 and airor other suitablegas is bubbled therethrough. A desiredfaniount of flotation reagents ls added and these reagents are active to separate the desired, materialsifrom the undesired Example I A volume of a-lead ore flotation pulp, correto a 2000 g. flotation cell. Then 0.008flb. of sodiumcyanide per ton of ore, 0.06lb. of Aerofloat No. '31 (a thiophosphoric acid +-6% thiocarbanilide) and the frother as listed below, were added. Air waspassed' through the pulp and a concen- Pounds 1 y Frother l 1 g on Percent Pb in con} centrate Percent Pb recovery 0% of equal vol. of pine oil and erosene+l0? Hercota 90% of same lend+10% sul- -Ionated castor oil 90% of same blcnd+l0% sulfonated inene-phenol con,- densate, asalt Example II I The same procedure as in ExampleI was followed.
, v Sodium cyanide lb...per ton of ore 0.008' Aerofioat No. 31 do 0.047 Flotation time es .20
Pounds per ton Percent Pb in cencentrate Percent Pb Frother I recovery Example III The same procedure as in Example I was followed, exdept neither collector (Aerofloat No. 31)
nor sodium cyanide was added. The frother was the only reagent present. Flotation time 20 minutes;-
. Pounds Percent Pb v Percent Pb Frother r in con- 811 centrate recovery 90% of equal vol. of pine oil and kerosene-+10% Hercota 0. l5 43. 7 88. 4 Same as above 0. l7 49. 8 k 01. 1 90% of equal vol. of pine oil and a kerosene+l0% sulfonated casa to! oil 0. 15 49. 8 87. Same as above 0. 17 47. l 88.
Example IV One thousand ten (1010) gfof St. .loseph Lead Company's Bonne Terre, Missouri, minus8 mesh ,lead ore were ground-in a ball mill for 12 minutes with 1000 cc. of distilled water. The ground ore'was screened through a 65 mesh screen'and .pulp were added the following fiothers, but no other reagents. The tests were carried out for 20 minutes.
v P d P t Pb can a ercen Percent Pb Frother per in concenton mm f P 90% of equal volume of pine' 'oil and kerosene+l0% Herwta. 0. 20 68. 88 80. 3 00% of above blend-{40% sulionated water oil 0. 20 68. 70 76. 6- 90% pine oll+l0% suliouated castor oil .L 0. 20 43. 73 76. 3
Example V Pounds Percent Pb' Percent Pb Frother in 313$]: v recovery I 90% of equal volume of pine oil +kerosene+l0% sull'onated pinene-phenol condensate, Na salt -3. 0. 20 65. 89 88. 4 90% of above blend-+10% sulfonated pinene-cresol condensate Na salt 0. 20 64. 25 86. 2 90% of e ual volumes of terpinyl I methy ether+kerosene+l0% s onated pinene-phenolconde te, Na salt 0. 20 64.91 :7. of above blend+l0% sulfeted dehydroabietylalcoliol, I 90; sfallggnifinii i yufiun 0.20 60.41 93.4
o a ve en erc ta 0.20 65.41 04.8
In the above, it will be noted that tests were made with blends containing a terpene ether (from terpineol and methyl alcohol) in place of pine oil. These ga e satisfactory results.
Example VI low, were added. Air was passed through the pulp and a concentrate was taken on for 20 Example VII About 830 g. of minus 8 mesh Matahambrecopper ore from Santa Lucia, Cuba, were ground in a ball mill for 14 minutes with 1000 cc.- of distilled water. The ground ore, was screened through a 48-mesh screen and then transferred to a 1000 g. flotation cell and further diluted to about 16% solids. 111 addition to the frother, the following materials were added to the pulp: Sodium cyanide lb. per ton of ore 0.10 Lime a [on 1.20 Potassium ethyl xanthate do 0.18
Air was passed throughthe pulp and a concentrate was taken off for 10 minutes.
Pounds Percent Cu Percent Cu Frother per in con- 1 ton centrate retovery 90% of equal vol. of pine oil and kerosene-{40% sulfonated castor oil 0. 58 18.87 90.3 90% of same blend+l% Hercota 0.58 l 19.77 91.0
Example VIII ores, of the metal bearing type. The pine oil blends utilized in carrying .out the process provide a relatively high recovery. Relatively small amounts of the blends are effective to separate the metals from the gangue in an expedient manner, thereby decreasing the cost of the frothing reagents and increasing the plant capacity.
It will be understood that the details and examples hereinbefore set forth are illustrative only and that theinvention-a's broadly described and claimed is in no way limited thereby,
What I claim and desire to protect by Letters Patent is:
pension of said ores in the presence of .a frothl. A process for the froth flotation of sulfide ores which comprises frothing an aqueous susing agent comprising major proportions of pine About 1030 g. of the same Matahambre copper ore were ground in a ballmill for 14 minutes with 1000 cc. of distilled water. The ground ore was screened througha 48-mesh screenand then transferred to a 1000 g. flotation cell and further diluted to about20% solids. In addition to the fr'other, the following-materials were added:
Sodium cyanide "lb. perton of ore 0.08 Li e" do 1.00 Potassium. ethyl xanthate do 0.15
Air was passed'through the pulp and a concentrate was taken off for 10 minutes.
dounds Percent Cu Percent Cu Frothcr per in concenton I trate F of equal vol. of pine oil and kerosene+10% sulfonated cas- 1 toroil 0.48 18:52 89.5 Same as above .5 1.' 0. 25 20. 62 89. 0 of equal vol. oipine oil and kerosene+5% sulfonated cas- 1 toroil 0.25 22.86 85.5;
o of equal vol. of pine oil and lvesso No. 2+10% sulfonated castlor %il E .ii .&. 0. 25- 20.86 84. 8 90%olequ 'vo.o place an Solvesso No. 3+10% sullonoted eastor oil. -.i .a- 0.24 21. 97 85.! 90% of equal vol. of pine oi an Solvesso No. 4+l0% sulfo noted castor oil I 0. 48 17. 23 91. 5
The last four frothers were stage fed, at
start, and /2 after 5 minutes of the test.
From the foregoing description and examples,
it will be seen that the present invention provides an improved froth flotation process for separating, collecting, or classifying minerals or oil and a hydrocarbon compound and .a minor proportion of an emulsifying agent selected from the group consisting of sulfonated pinene-cresol condensate, sulfonated pinene-phenol condensate, sulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters, ethanolamine-castor oil- -condensates and triethanolamine-castor oil condensates. 2. A processfor the froth flotation of sulfide ores which comprises frothing an aqueous suspension of' said ores in the presence of a frothing agent comprising major proportions of pine oil and a hydrocarbon compound and a minor proportion of an ethanolamine-castor oil condensate.
ores which comprises frothing an aqueous suspension of .said ores in the presence of a frothing agent comprising major proportions of pineoil and a hydrocarbon compound and a minor proportion of a triethanolamine-castor oil condensate.
4. A process for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said ores in the presence of a frothing agent comprising major proportions of pine oil 7 and a hydrocarbon-compound having a boiling range between about 100 C. and about 300 C. and a minor proportion of an emulsifyingagent selected from the group consisting of sulfonated pinene-cresol condensate, sulfonated pinenephenol condensate, sulfated dehydroabietyl alcohol, sulfonated higher fatty acid esters,
ethanolamine-castor oil condensates and triethanolamine-castor oil condensates.
5. A- process for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said ores in. the presence of 'a frothing agent comprising major proportions of pine oil and a hydrocarbon compound and from about 1 to about 25% of an emulsifying agent selected from the group consisting ofsulfonated pinenecresol condensate, sulfonated pinene phenol condensate. sulfated dehydroabietyl alcohol, sulfonated higher fatty acid .esters, ethanolaminecastor oil condensates and triethanolaminecastor oil condensates.
6. A processfor the froth flotationof sulfide.-
dehydroabietyl alcohol, sulfonated higher fatty acid esters, ethanolamine castor oil condensates and triethanolamine-castor oil condensates.-
3. A process for the froth flotation of sulfide.
7. A process for the froth flotation of sulfide ores whichcomprises frothing an aqueous suspension of said ores in-the presence of a frothing agent comprising major proportions of terpinyl methyl ether and kerosene and a. minor. 5 .proportion of. an ethanolamine-castor oil.condensate. r
8. A proeess for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of said oresin the presence of a irothi'ng m agent comprising substantially equal volumes of a commercial pine oil-and kerosene and about 10% of an ethanolamine-castor oil condensate.
9. In a process for the froth flotation of sulfide ores which comprises frothing an aqueous suspension of, said ores in the presence of .a frothin'g agent comprising major proportions of pine oil and kerosene and a minorproportion of sulfonated castor oil.
- PHILIP A. RAY.,
g lt 3m? lid; 2, 236571;;
CERTIFICATE OF comcmox v mm 1 6, 191:.2. PHILIP: A; my.
yIt' in harsh, cahti-fld' that qrroznapbear'a m the p'rintQd sp e cifleation brim; above fii b'er' a .pdc m't requiring correction as rollown; Page 2, first palm, 11116 1,. in tpe ble, for "or read. -'---90$--;; and that the said Let-
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US304707A US2286374A (en) | 1939-11-16 | 1939-11-16 | Flotation process |
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US304707A US2286374A (en) | 1939-11-16 | 1939-11-16 | Flotation process |
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US2286374A true US2286374A (en) | 1942-06-16 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2636604A (en) * | 1949-06-17 | 1953-04-28 | Bethlehem Steel Corp | Flotation of pyrites from a pyrite ore pulp |
US2959713A (en) * | 1955-11-21 | 1960-11-08 | Minnesota Mining & Mfg | Circuit controlling device |
US3094484A (en) * | 1958-08-22 | 1963-06-18 | R Alfonso Rizo-Patron | Process of froth flotation of ores |
US4514292A (en) * | 1983-11-09 | 1985-04-30 | Hercules Incorporated | Froth flotation process |
-
1939
- 1939-11-16 US US304707A patent/US2286374A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2636604A (en) * | 1949-06-17 | 1953-04-28 | Bethlehem Steel Corp | Flotation of pyrites from a pyrite ore pulp |
US2959713A (en) * | 1955-11-21 | 1960-11-08 | Minnesota Mining & Mfg | Circuit controlling device |
US3094484A (en) * | 1958-08-22 | 1963-06-18 | R Alfonso Rizo-Patron | Process of froth flotation of ores |
US4514292A (en) * | 1983-11-09 | 1985-04-30 | Hercules Incorporated | Froth flotation process |
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