US3061097A - Flotation process for separating bituminous matter from associated gangue minerals - Google Patents

Flotation process for separating bituminous matter from associated gangue minerals Download PDF

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US3061097A
US3061097A US782766A US78276658A US3061097A US 3061097 A US3061097 A US 3061097A US 782766 A US782766 A US 782766A US 78276658 A US78276658 A US 78276658A US 3061097 A US3061097 A US 3061097A
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flotation
ore
bituminous
froth
ton
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Dering Roger
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JACK B DARRAGH
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/002Inorganic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/006Hydrocarbons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/008Organic compounds containing oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/016Macromolecular compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/002Coagulants and Flocculants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/007Modifying reagents for adjusting pH or conductivity
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/04Frothers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/06Depressants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2203/00Specified materials treated by the flotation agents; Specified applications
    • B03D2203/006Oil well fluids, oil sands, bitumen

Definitions

  • a principal object of this invention is to provide a flotation process for eifectively separating, organic carbonaceous materals from rock and other inorganic mineral matter with which they are intimately associated.
  • a more specific object is to provide a practical, commercial process for producing from oil shale a high-kerogen material for conversion into shale oil and other products.
  • An outstanding feature of the invention is the subjecting of a flotation pulp of the material to flotation in the presence of a suitable pine distillate and a super-normal quantity of a coal tar creosote.
  • the carbonaceous material is floated off as a froth concentrate.
  • FIGURE is a flow sheet showing the preferred procedure as applied to oil shale.
  • the kerogen content of oil shale is in the form of solid particles distributed throughout the fine-grained, sedimentary, host rock. Oftentimes asphaltite and parafline residues are physically associated with the kerogen. These 65 organic carbonaceous materials are not readily wettable, although the associated rock may be easily wetted in accordance with long established practice in the flotation art.
  • the secondary crushing stage is carried out wet to prevent pyrolysis. Grinding should not be excessive, and, to this end, is preferably carried out with large balls or rods.
  • a super-normal quantity e.g. 0.5-2.0 lbs./ton of ore depending upon thecharacter of the ore
  • coal tarcreosote such as Barrett No. 4
  • Another special reagent having very little if any frothing properties is also employed as a promoter for the organic values- This is a complex combination of monocyclic terpene hydrocarbons normally derived from the destructive distillation of pine and containing pinenes and terpineols. It has limited solvent properties with respect to the organic carbonaceous matter to be recovered.
  • the material Solvenol is somewhat variable in composition, but the following is typical:
  • a silica depressant such as sodium silicate, is also utilized where necessary, e.g. with oil and asphaltic shales and bituminous sands. It is not necessary with the uranium ores of my afore-referred-to copending application.
  • Both it and the coal tar creosote are preferably added to the pulp in the grinding circuit. From about 0.1 to 3.0
  • pounds per ton of ore are used depending upon the quantity and physical characteristics of the silica present.
  • the pulp from the grinding circuit is advantageously conditioned in the usual conditioning equipment with a
  • the shale is first crushed tetrachloride, such as perchloroethylene, which acts as a depressant on barren colloidal slirnes and also aids in loosening the wax and asphalt from association with the mineral particles.
  • This reagent also exhibits some collection properties with respect to the kerogen and other organic carbonaceous materials. From about 0.1 to 3.0 pounds per ton of ore are used depending upon the organic content and characteristics of the ore.
  • the pulp is subjected to primary flotation in the usual equipment, advantageously in the presence of a non-reactive, neutral frother selective as to the non-wetted bituminous particles.
  • a long chain alcohol such as Dowfroth 250 or Aerofroth (both well known commercial reagents)
  • Dowfroth 250 or Aerofroth both well known commercial reagents
  • any of the well-known nonreactive frothers such as pine oil, eucalyptus oil, and amyl acetate, may also be employed. From about 0.02 to 0.10 pound per ton of ore are used, depending upon the froth conditions and scavenging requirements.
  • the special 5 rial passed to a second conditioning stage, where one of the well-known flocculating agent, such as Dow Separan' 2610 or American Cyanamid Aerofloc 548," is added as a slime depressant, and where, if calcite is present, a calcite depressant, such as a tannin derivative, is added in accordance with usual practice in the flotation art.
  • one of the well-known flocculating agent such as Dow Separan' 2610 or American Cyanamid Aerofloc 548
  • a calcite depressant such as a tannin derivative
  • the so-conditioned tails are then subjected to secondary flotation, utilizing the SolvenoP type of reagent in quantity of about 0.05 to 0.10 pound per ton of ore and the neutral selective frother (long chain alcohol) in quantity of about 0.02 to 0.10 pound per ton of ore.
  • the concentrate from this secondary flotation is passed to the cleaner cell along with the rougher concentrate of the primary flotation, while the tails are passed to waste.
  • the cleaner flotation of concentrates is carried out using a slime depressant reagent (a poly-electrolytic settling agent, such as American Cyanamid Aerofloc, or some other high molecular polymer flocculant such as Dow Separan) and the aforementioned neutral selective frother in quantities of from about 0.01 to 0.05 and 0.01 to 0.10 pound per ton of ore, respectively.
  • a slime depressant reagent a poly-electrolytic settling agent, such as American Cyanamid Aerofloc, or some other high molecular polymer flocculant such as Dow Separan
  • the final concentrate is a high-kerogen material which may be processed in some suitable manner, as, for example, by retorting, to produce shale oil and other products.
  • the tails were scoured and classified.
  • the plus 200 mesh material was discarded, but the minus 200 mesh material was conditioned for six minutes with 0.02 lbs/ton of Separan 2610" and with 0.05 lbs/ton of Quebracho (a tannin derivative).
  • the conditioned pulp was then passed to secondary flotation, where 0.05 lb./ton of Solvenol and 0.05 lb./ton of Dowfroth 250" were added and flotation carried out for eight minutes.
  • the tails were discarded.
  • the froth concentrates from both primary and secondary flotation were passed to cleaner flotation, and 0.01 lb./ ton of Aerofloc 548 and 0.05 lb./ton of Dowfroth" were added. Flotation of these froth concentrates was carried out for twelve minutes.
  • a flotation process for the separation of bituminous material, such as kerogen, asphaltites, and paraflines, from associated inorganic gangue materials comprising subjecting a flotation pulp of the materials to conditioning with a tetrachloride; subjecting the conditioned pulp to frothflotation in the presence of eflective quantities of a complea of monocyclic terpene hydrocarbons, derived from the destructive distillation of pine, and of coal tar creosote, to produce a froth which is high in bituminous materials and a tails which is low in bituminous materials; and separating said froth from said tails.
  • bituminous material such as kerogen, asphaltites, and paraflines
  • a froth flotation process for the separation of the lcerogen and other bituminous content of oil shale comprising subjecting a flotation pulp of an oil shale to conditioning with a tetrachloride; and subjecting the conditioned pulp to froth flotation in the presence of an effective quantity of a complex of monocyclic terpene hydrocarbon derived from the destructive distillation of pine, and effective quantities of coal tar creosote, of a silica depressant, and of a non-reactive neutral frother reagent selective to the kerogen and other bituminous materials.
  • a flotation process for the separation of bituminous material, such as kerogen, asphaltities, and paraflines, from associated inorganic gangue in an ore material comprising subjecting a flotation pulp of the ore material to froth flotation in the presence of a complex of monocyclic terpene hydrocarbons derived from the destructive distillation of pine and in quantity of from about 0.1 to i 0.3 pound per ton of ore material, coal tar creosote in quantity of from about 0.5 to 2.0 pounds per ton of ore material, and a non-reactive neutral frother in quantity of from about 0.02 to 0.10 per ton of ore material, to produce a froth which is high in bituminous material and a tails which is low in bituminous material said complex having very little or no frothing characteristics as compared with pine oil and having only limited solvent action with respect to said bituminous material; and separating said froth from said tails.
  • bituminous material such as kerogen,
  • a froth flotation process for the separation of the kerogen and other bituminous content of oil shales from the rock with which they are associated comprising subjecting a flotation pulp of an oil shale to froth flotation in the presence of a complex of monocyclic terpene hydrocarbons derived from the destructive distillation of pine and in quantity of from about 0.1 to 0.3 pound per ton of oil shale, coal tar creosote in quantity of from about 0.5 to 2.0 pounds per ton of oil shale and a nonreactive neutral frother reagent selective to the kerogen and other bituminous mat ials, said frother reagent be- 2,750,036 Hunter et al.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Removal Of Floating Material (AREA)

Description

Oct. 30, 1962 MATTER FROM ASSOCIATED RING R. DE FLOTATION PROCESS FOR SEPARATING BITUMINOUS GANGUE MINERALS Filed Dec. 24, 1958 OIL SHALE WATER CRUSHER PULP CONDITIONER PERCHLORETHYLENE NON-REACTIVE PULP FROTHER PINE DISTILLATE (Long chaln alcohol) (Monocycllc ferpene hydrocarbons) FROTH FLOTATION P H f f (Rougher Concentrate) (lrlmary o 0 Ion) f 53T TAILS FLOTATION Concentrate) I MACHI NE oncen ra e DUTC lCleanmg) I +200 MESH -2OO MESH F|QQH| AN]: TAILS TANNIN To WASTE (if calcite present) To WASTE CONDITIONER END PRODUCT p p (Keroqen NoN-F ;%c T l\ U PINE DISTILLATE l gsapgc lpgfee M I 1 r (Long chain alcohol) Ly g; rh%ns Concemrofe) I F ROTH F LOTATION (Concentrate) MACHINE (Secondary FIOTCITIOII) I TAILS TO WASTE INVENTOR. ROGER DERING. MM J, MM
ATTORNEYS United States Patent 3061 091 FLOTATION PRocFssFoh SEPARATING BITUMI- NOUS MATTER FROM ASSOCIATED GANGUE This invention relates to processes of flotation, and is particularly concerned with the separation by flotation of bituminous or organic carbonaceous materials, such as kerogen, asphaltities, and parafiines, from the host rock or other earth materials with which they are associated in nature.
In my copending application Serial No. 485,215, now Patent No. 2,890,795, filed January 31, l955,-entitled, Metallurgical Processing of Uranium Ores, I have disclosed certain aspects of the present invention as a part of the over-all processing of uranium ore for the recovery of uranium values. There, the organic carbonaceous material, usually asphaltite, carries uranium values, but is separated from uranium-bearinginorganic portions of the ore by flotation so that it may be ifidependently processed for the recovery of the uranium.
I have found that essentially the same flotation procedure is applicable to the recovery of organic carbonaceous materials, such as kerogen and associated asphaltite and parafline found in oil shales, the bituminous material in bituminous sands and sandstone, and the asphaltic material in asphaltic shales, when those are the values sought.
A principal object of this invention is to provide a flotation process for eifectively separating, organic carbonaceous materals from rock and other inorganic mineral matter with which they are intimately associated.
A more specific object is to provide a practical, commercial process for producing from oil shale a high-kerogen material for conversion into shale oil and other products.
An outstanding feature of the invention is the subjecting of a flotation pulp of the material to flotation in the presence of a suitable pine distillate and a super-normal quantity of a coal tar creosote. The carbonaceous material is floated off as a froth concentrate.
Further objects and features will become apparent from the following detailed description of the presently preferred procedure illustrated by way of example in the accompanying drawing.
In the drawing, the single FIGURE is a flow sheet showing the preferred procedure as applied to oil shale.
The kerogen content of oil shale is in the form of solid particles distributed throughout the fine-grained, sedimentary, host rock. Oftentimes asphaltite and parafline residues are physically associated with the kerogen. These 65 organic carbonaceous materials are not readily wettable, although the associated rock may be easily wetted in accordance with long established practice in the flotation art.
and ground to a size suitable for flotation, e.g. to minus 80 mesh. The secondary crushing stage is carried out wet to prevent pyrolysis. Grinding should not be excessive, and, to this end, is preferably carried out with large balls or rods.
3,061,097 Patented Oct. 30, 1062 In accordance with the invention, a super-normal quantity (e.g. 0.5-2.0 lbs./ton of ore depending upon thecharacter of the ore) of coal tarcreosote such as Barrett No. 4, is employed as a collector for the kerogen. Another special reagent having very little if any frothing properties is also employed as a promoter for the organic values- This is a complex combination of monocyclic terpene hydrocarbons normally derived from the destructive distillation of pine and containing pinenes and terpineols. It has limited solvent properties with respect to the organic carbonaceous matter to be recovered. An example of such material is the proprietary product *Solvenol marketed by Hercules Powder Co. It is used in quantity of from about 0.1 to 0.3 pound per ton of ore, depending upon the character of the ore, it being realized that the values sought are strongly hydrophobic and this reagent has a selective affinity therefor.
The material Solvenol is somewhat variable in composition, but the following is typical:
A silica depressant, such as sodium silicate, is also utilized where necessary, e.g. with oil and asphaltic shales and bituminous sands. It is not necessary with the uranium ores of my afore-referred-to copending application.
' Both it and the coal tar creosote are preferably added to the pulp in the grinding circuit. From about 0.1 to 3.0
pounds per ton of ore are used depending upon the quantity and physical characteristics of the silica present.
The pulp from the grinding circuit is advantageously conditioned in the usual conditioning equipment with a As indicated in the flow sheet, the shale is first crushed tetrachloride, such as perchloroethylene, which acts as a depressant on barren colloidal slirnes and also aids in loosening the wax and asphalt from association with the mineral particles. This reagent also exhibits some collection properties with respect to the kerogen and other organic carbonaceous materials. From about 0.1 to 3.0 pounds per ton of ore are used depending upon the organic content and characteristics of the ore.
Following this conditioning stage, the pulp is subjected to primary flotation in the usual equipment, advantageously in the presence of a non-reactive, neutral frother selective as to the non-wetted bituminous particles. A long chain alcohol, such as Dowfroth 250 or Aerofroth (both well known commercial reagents), is very satisfactory, although practically any of the well-known nonreactive frothers, such as pine oil, eucalyptus oil, and amyl acetate, may also be employed. From about 0.02 to 0.10 pound per ton of ore are used, depending upon the froth conditions and scavenging requirements. The special 5 rial passed to a second conditioning stage, where one of the well-known flocculating agent, such as Dow Separan' 2610 or American Cyanamid Aerofloc 548," is added as a slime depressant, and where, if calcite is present, a calcite depressant, such as a tannin derivative, is added in accordance with usual practice in the flotation art.
The so-conditioned tails are then subjected to secondary flotation, utilizing the SolvenoP type of reagent in quantity of about 0.05 to 0.10 pound per ton of ore and the neutral selective frother (long chain alcohol) in quantity of about 0.02 to 0.10 pound per ton of ore. The concentrate from this secondary flotation is passed to the cleaner cell along with the rougher concentrate of the primary flotation, while the tails are passed to waste.
The cleaner flotation of concentrates is carried out using a slime depressant reagent (a poly-electrolytic settling agent, such as American Cyanamid Aerofloc, or some other high molecular polymer flocculant such as Dow Separan) and the aforementioned neutral selective frother in quantities of from about 0.01 to 0.05 and 0.01 to 0.10 pound per ton of ore, respectively.
The final concentrate is a high-kerogen material which may be processed in some suitable manner, as, for example, by retorting, to produce shale oil and other products.
The following example with respect to oil shale is typical of many laboratory tests carried out with substantially similar results:
Example One kilogram of an oil shale taken from T-6-S, R-6-E near Soldier Summit, Utah, was crushed to 8 mesh and ground in a laboratory ball mill to minus 80 mesh. Coal tar creosote was added to the ball mill on the basis of 1% lbs. per dry ton of ore. Sodium silicate (commercial) was added to the ball mill on the basis of 3 lbs./ton, along with one kilogram of water (100 gms. of water was added earlier in the secondary crushing stage using a gyratory type, laboratory crusher). The ball mill discharge was conditioned six minutes with 1 lb./ton perchlorethylene (C 01 The conditioned pulp was run into a l000 gm. laboratory flotation cell, and 0.15 lb./ton of Solvenol" added. The first stage of primary flotation was carried out for four minutes, after which 0.10 lb./ton of Dowfroth 250 was added and a scavenging flotation stage carried out for four minutes.
The tails were scoured and classified. The plus 200 mesh material was discarded, but the minus 200 mesh material was conditioned for six minutes with 0.02 lbs/ton of Separan 2610" and with 0.05 lbs/ton of Quebracho (a tannin derivative). The conditioned pulp was then passed to secondary flotation, where 0.05 lb./ton of Solvenol and 0.05 lb./ton of Dowfroth 250" were added and flotation carried out for eight minutes. The tails were discarded. p
The froth concentrates from both primary and secondary flotation were passed to cleaner flotation, and 0.01 lb./ ton of Aerofloc 548 and 0.05 lb./ton of Dowfroth" were added. Flotation of these froth concentrates was carried out for twelve minutes.
The final froth was filtered and volatilized in an electric It can be seen from these results that over 91% of the bituminous materials was recovered, while eliminating over 93% of the inorganic gangue. The percent volatiles was increased from over 37% in the raw shale to over 83% in the final material, indicating a ratio of concentration of 2.43:1. 4
Whereas this process has been illustrated and described with respect to a particular preferred application thereof in practice, it should be realized that the invention is not limited to the specific procedures set forth, and that such procedures may be varied by those skilled in the art within the scope of the claims which here follow.
I claim:
1. A flotation process for the separation of bituminous material, such as kerogen, asphaltites, and paraflines, from associated inorganic gangue materials, comprising subjecting a flotation pulp of the materials to conditioning with a tetrachloride; subjecting the conditioned pulp to frothflotation in the presence of eflective quantities of a complea of monocyclic terpene hydrocarbons, derived from the destructive distillation of pine, and of coal tar creosote, to produce a froth which is high in bituminous materials and a tails which is low in bituminous materials; and separating said froth from said tails.
. 2. The flotation process of claim 1, wherein a silica depressant is also used as a reagent in the froth flotation of the bituminous materials.
3. The flotation process of claim 1, wherein a non-reactive, neutral frother (long chain alcohol) is also used in the froth flotation of the bituminous materials.
4. The flotation process of claim 3, wherein the tails are conditioned with a flocculating agent and subjected to secondary flotation with more of the special pine derivative reagent and long chain alcohol.
5. The flotation process of claim 4, wherein the froth from both the primary and the secondary flotation stages is subjected to cleaner flotation in the presence of a flora culating agent and more of the long chain alcohol.
6. A froth flotation process for the separation of the lcerogen and other bituminous content of oil shale: from the rock with which they are associated, comprising subjecting a flotation pulp of an oil shale to conditioning with a tetrachloride; and subjecting the conditioned pulp to froth flotation in the presence of an effective quantity of a complex of monocyclic terpene hydrocarbon derived from the destructive distillation of pine, and effective quantities of coal tar creosote, of a silica depressant, and of a non-reactive neutral frother reagent selective to the kerogen and other bituminous materials.
7. The flotation process of claim 6, wherein the nonreactive frother reagent is a long chain alcohol.
8. A flotation process for the separation of bituminous material, such as kerogen, asphaltities, and paraflines, from associated inorganic gangue in an ore material, comprising subjecting a flotation pulp of the ore material to froth flotation in the presence of a complex of monocyclic terpene hydrocarbons derived from the destructive distillation of pine and in quantity of from about 0.1 to i 0.3 pound per ton of ore material, coal tar creosote in quantity of from about 0.5 to 2.0 pounds per ton of ore material, and a non-reactive neutral frother in quantity of from about 0.02 to 0.10 per ton of ore material, to produce a froth which is high in bituminous material and a tails which is low in bituminous material said complex having very little or no frothing characteristics as compared with pine oil and having only limited solvent action with respect to said bituminous material; and separating said froth from said tails.
9. A froth flotation process for the separation of the kerogen and other bituminous content of oil shales from the rock with which they are associated, comprising subjecting a flotation pulp of an oil shale to froth flotation in the presence of a complex of monocyclic terpene hydrocarbons derived from the destructive distillation of pine and in quantity of from about 0.1 to 0.3 pound per ton of oil shale, coal tar creosote in quantity of from about 0.5 to 2.0 pounds per ton of oil shale and a nonreactive neutral frother reagent selective to the kerogen and other bituminous mat ials, said frother reagent be- 2,750,036 Hunter et al. June 12, 1956 ing used in quantity of from about 0.02 to 0.10 pound 2,973,864 McGan-y Mar. 7, 1961 per ton of oil shale. v FOREIGN PATENTS References Cited in the file of this patent 5 201,406 Switzerland Sept. 1, 1939 UNITED STATES PATENTS OTHER REFERENCES 1,510,983 Dolbear Oct. 7, 1924. Taggart: "Handbook of Mineral Dressing," 194S, sec.
1,761,546 Trotter et a]. June 3, 1930 I 12, pages 44 and45.

Claims (1)

  1. 9. A FROTH FLOTATION PROCESS FOR THE SEPARATION OF THE KEROGEN AND OTHER BITUMINOUS CONTENT OF OIL SHALES FROM
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US3252662A (en) * 1962-08-20 1966-05-24 Monsanto Co Sulfide ore beneficiation
US4506835A (en) * 1982-05-06 1985-03-26 Occidental Research Corp. Oil shale beneficiation
WO2006071672A2 (en) * 2004-12-23 2006-07-06 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US20060151397A1 (en) * 2004-12-23 2006-07-13 Georgia-Pacific Resins, Inc. Amine-aldehyde resins and uses thereof in separation processes
US20070000839A1 (en) * 2004-12-23 2007-01-04 Georgia-Pacific Resins, Inc. Modified amine-aldehyde resins and uses thereof in separation processes
US20070012630A1 (en) * 2004-12-23 2007-01-18 Georgia-Pacific Resins, Inc. Amine-aldehyde resins and uses thereof in separation processes
US20080017552A1 (en) * 2004-12-23 2008-01-24 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US20080029460A1 (en) * 2004-12-23 2008-02-07 Georgia-Pacific Chemicals Llc. Amine-aldehyde resins and uses thereof in separation processes
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WO2009114145A2 (en) * 2008-03-11 2009-09-17 Verutek Technologies, Inc. Ex-situ low-temperature hydrocarbon separation from tar sands
WO2010104516A1 (en) * 2009-03-13 2010-09-16 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
US8101812B2 (en) 2007-09-20 2012-01-24 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials
US8272442B2 (en) 2007-09-20 2012-09-25 Green Source Energy Llc In situ extraction of hydrocarbons from hydrocarbon-containing materials
US8404108B2 (en) 2007-09-20 2013-03-26 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials

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US1510983A (en) * 1920-11-11 1924-10-07 Edwin Letts Oliver Method of concentrating oil shales
US1761546A (en) * 1929-03-01 1930-06-03 Minerals Separation North Us Concentration of phosphate-bearing material
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US1761546A (en) * 1929-03-01 1930-06-03 Minerals Separation North Us Concentration of phosphate-bearing material
CH201406A (en) * 1937-11-05 1938-11-30 Oerlikon Maschf Transformer with devices for suppressing harmonics in the magnetizing current.
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US2973864A (en) * 1955-01-06 1961-03-07 Int Minerals & Chem Corp Process for beneficiation of asphaltite material

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Publication number Priority date Publication date Assignee Title
US3252662A (en) * 1962-08-20 1966-05-24 Monsanto Co Sulfide ore beneficiation
US4506835A (en) * 1982-05-06 1985-03-26 Occidental Research Corp. Oil shale beneficiation
US8011514B2 (en) 2004-12-23 2011-09-06 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US8127930B2 (en) 2004-12-23 2012-03-06 Georgia-Pacific Chemicals Llc Amine-aldehyde resins and uses thereof in separation processes
US20060151397A1 (en) * 2004-12-23 2006-07-13 Georgia-Pacific Resins, Inc. Amine-aldehyde resins and uses thereof in separation processes
US8757389B2 (en) 2004-12-23 2014-06-24 Georgia-Pacific Chemicals Llc Amine-aldehyde resins and uses thereof in separation processes
US20070012630A1 (en) * 2004-12-23 2007-01-18 Georgia-Pacific Resins, Inc. Amine-aldehyde resins and uses thereof in separation processes
WO2006071672A3 (en) * 2004-12-23 2007-02-08 Georgia Pacific Resins Modified amine-aldehyde resins and uses thereof in separation processes
US20080017552A1 (en) * 2004-12-23 2008-01-24 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US8092686B2 (en) 2004-12-23 2012-01-10 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US8702993B2 (en) 2004-12-23 2014-04-22 Georgia-Pacific Chemicals Llc Amine-aldehyde resins and uses thereof in separation processes
US20060151360A1 (en) * 2004-12-23 2006-07-13 Georgia-Pacific Resins, Inc. Modified amine-aldehyde resins and uses thereof in separation processes
US10150839B2 (en) 2004-12-23 2018-12-11 Ingevity South Carolina, Llc Amine-aldehyde resins and uses thereof in separation processes
US7913852B2 (en) 2004-12-23 2011-03-29 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US20080029460A1 (en) * 2004-12-23 2008-02-07 Georgia-Pacific Chemicals Llc. Amine-aldehyde resins and uses thereof in separation processes
US20070000839A1 (en) * 2004-12-23 2007-01-04 Georgia-Pacific Resins, Inc. Modified amine-aldehyde resins and uses thereof in separation processes
WO2006071672A2 (en) * 2004-12-23 2006-07-06 Georgia-Pacific Chemicals Llc Modified amine-aldehyde resins and uses thereof in separation processes
US8272442B2 (en) 2007-09-20 2012-09-25 Green Source Energy Llc In situ extraction of hydrocarbons from hydrocarbon-containing materials
US9181468B2 (en) 2007-09-20 2015-11-10 Green Source Holdings Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
JP2010540694A (en) * 2007-09-20 2010-12-24 グリーン・ソース・エナジー・リミテッド・ライアビリティ・カンパニー Hydrocarbon extraction from hydrocarbon-containing materials
US9416645B2 (en) 2007-09-20 2016-08-16 Green Source Holdings Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
US8404107B2 (en) 2007-09-20 2013-03-26 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials
US8404108B2 (en) 2007-09-20 2013-03-26 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
US8522876B2 (en) 2007-09-20 2013-09-03 Green Source Energy Llc In situ extraction of hydrocarbons from hydrocarbon-containing materials
US8685234B2 (en) 2007-09-20 2014-04-01 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
WO2009038728A1 (en) * 2007-09-20 2009-03-26 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials
US8101812B2 (en) 2007-09-20 2012-01-24 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials
EA023805B1 (en) * 2007-09-20 2016-07-29 Грин Сорс Энерджи Ллк Extraction of hydrocarbons from hydrocarbon-containing materials
US8926832B2 (en) 2007-09-20 2015-01-06 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials
US9102864B2 (en) 2007-09-20 2015-08-11 Green Source Holdings Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
WO2009114145A2 (en) * 2008-03-11 2009-09-17 Verutek Technologies, Inc. Ex-situ low-temperature hydrocarbon separation from tar sands
WO2009114145A3 (en) * 2008-03-11 2010-05-14 Verutek Technologies, Inc. Ex-situ low-temperature hydrocarbon separation from tar sands
AU2009341831B2 (en) * 2009-03-13 2014-11-06 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
WO2010104516A1 (en) * 2009-03-13 2010-09-16 Green Source Energy Llc Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
EA024263B1 (en) * 2009-03-13 2016-09-30 Грин Сос Энерджи Ллк Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials

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