US2875896A - Process of concentrating columbium minerals by froth flotation - Google Patents
Process of concentrating columbium minerals by froth flotation Download PDFInfo
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- US2875896A US2875896A US689435A US68943557A US2875896A US 2875896 A US2875896 A US 2875896A US 689435 A US689435 A US 689435A US 68943557 A US68943557 A US 68943557A US 2875896 A US2875896 A US 2875896A
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- columbium
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- 238000000034 method Methods 0.000 title claims description 40
- 239000010955 niobium Substances 0.000 title claims description 38
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 title claims description 36
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims description 28
- 239000011707 mineral Substances 0.000 title claims description 28
- 238000009291 froth flotation Methods 0.000 title claims description 11
- 239000003153 chemical reaction reagent Substances 0.000 claims description 41
- 239000012141 concentrate Substances 0.000 claims description 23
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims description 20
- 229960003540 oxyquinoline Drugs 0.000 claims description 16
- 239000000470 constituent Substances 0.000 claims description 7
- 238000000926 separation method Methods 0.000 claims description 5
- 238000012360 testing method Methods 0.000 description 34
- 238000005188 flotation Methods 0.000 description 30
- 238000011084 recovery Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 9
- 239000002699 waste material Substances 0.000 description 8
- 239000007791 liquid phase Substances 0.000 description 7
- 230000001143 conditioned effect Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 4
- 229910021532 Calcite Inorganic materials 0.000 description 3
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000005273 aeration Methods 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 239000010430 carbonatite Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 229910052569 sulfide mineral Inorganic materials 0.000 description 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- -1 IRON SULFIDE SULFIDES Chemical class 0.000 description 2
- 229910052586 apatite Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000007885 magnetic separation Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- NBYLBWHHTUWMER-UHFFFAOYSA-N 2-Methylquinolin-8-ol Chemical compound C1=CC=C(O)C2=NC(C)=CC=C21 NBYLBWHHTUWMER-UHFFFAOYSA-N 0.000 description 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 1
- OYUKRQOCPFZNHR-UHFFFAOYSA-N 4-methylquinolin-8-ol Chemical compound C1=CC=C2C(C)=CC=NC2=C1O OYUKRQOCPFZNHR-UHFFFAOYSA-N 0.000 description 1
- AIBOXZCUYYHFTM-UHFFFAOYSA-N 6-methylquinolin-8-ol Chemical compound N1=CC=CC2=CC(C)=CC(O)=C21 AIBOXZCUYYHFTM-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002015 acyclic group Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000763 evoking effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 229910001729 niobium mineral Inorganic materials 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 238000004094 preconcentration Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001773 titanium mineral Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
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
- B03D1/01—Organic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B34/00—Obtaining refractory metals
- C22B34/20—Obtaining niobium, tantalum or vanadium
- C22B34/24—Obtaining niobium or tantalum
-
- 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
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
Definitions
- This invention relates to the art of froth flotation for the selective recovery of specific minerals from their ores. It has particular reference to the recovery of columbium minerals from the ores in which they are found.
- Another feature useful in minimizing reagent consumption is the reclaiming of the reagent-bearing solution from the final flotation pulp, and the use of same in preparing the initial flotation pulp for a subsequent run.
- This is advantageously done in connection with still another feature of the invention, namely, preliminary treatment of the ore for the elimination of various gangue ment for gangue elimination is dewatered. It is then re-pulped in recovered reagent-bearing solution prior to undergoing the significant froth flotation stage of the process.
- columbium minerals may be effectively and economically floated from "gangue constituents of an ore by the use of a reagent selected from a. particular group of chemical compounds, serving as' a collector selective to such columbium minerals.
- the group of chemical compounds consists of a hydroxyquinoline, specifically, 8-quinolinol, commonly known as oxine, and mono-lower-alkyl-substituted 8-quinolinols.
- 8-quinolinol is well known as a chemical com pound, it is normally used in highly purified form in the chemical art as an analytical reagent.
- the only instances where 8-quinolinol has even been triedas a flotation reagent is in connection with certain academic investigations concerned with abstract flotationtheory. In such instances, the materials involved were merely artificial mixtures containing solely zinc, iron, tungsten, and Such experiments have evoked little interest, and have given no indication that the particular reagent has any eifectiveness as applied to columbium.
- the ore is finely ground in a manner customary in conventional flotation practice, and is subjected to agitation and aeration, as an aqueous pulp, in the presence of the particular reagent specified.
- the columbium minerals are effectively collected in the froth,- to yield a columbium concentrate.
- the resulting upgraded ore pulp (from 0.6 percent Cb O to 2.36 percent Cb O was deslimed, and the deslimed pulp conditioned with 2 grams of C. P. 8-quinolinol and 1.5 grams of burner oil for flotation.
- Test No. 1 (8-quin0linol) Five hundred grams of a low grade carbonate type ore containing the columbium minerals Pyrochlore and Perovs kite and upgraded by removal of calcite and apatite, by desliming, and by removal of iron sulfide and magnetite were subjected to a batch flotation procedure involving flotation at pH 7.2 to 8.0 for ten minutes in the presence of two and one-half grams of 8-quinolinol. The rougher froth concentrate obtained was cleaned by reflotation, with the following results:
- Test No. 3 (4-methyl-8- quinolinol)' The procedure here was identical with the foregoing tests, except 2.0 grams of4-methyl-8-quinolinol were used as the collector reagent. Results were as follows:
- Test N0. 4 (6-methyl-8-quirtolinol) The procedure here was identical with the foregoing tests, except 2.0 grams of 6-methyl-8-quinolinol were used as the collector reagent. Results were as follows:
- a process of froth flotation for the separation of columbium minerals from other constituents of a columbium ore the steps of agitating and aerating an aqueous pulp containing said columbium ore and a collector reagent selected from'the group consisting of 8- quinolinol and mono-lower-alkyl-substituted 8-quinolinols; and recovering the resulting froth as a columbium concentrate.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
March 1959 A. w. LAST ET AL A PROCESS: OF CONCENTRATING COLUMBIUM MINERALS BY FROTH FLOTATION Filed 001;. 10. 1957 NIoBIuNI 0R l -AQUEOUS PULP T ?;%IF OPTIONAI. f T0 WASTE TAILINGS I A SLIMES A DESLIMING OPTIONAI. F I To WASTE sA Ds k MICA AND IRON MlCA AND IRON SULFIDE SULFIDES FROTH CONCENTRATES OPTIONAL FLOTATIQN TO WASTE TAIL INGS MAONE'TITE MAGNETIC SEPARATION OPTIONAL I TO WASTE I AQUEOUS PU l P w F I FILTER rFlLTRATE TO WASTE I CAKE i F REPULPING l AQUEOUS PULP BURNER OlL-- 1 --a-QuINOI INOI FROTH FLOTATION I I NIOBIUMI-BEARING TAILINGS FROTH FFILTERJ FFILTERJ l l CAKE CAKE FILTRATE FILTRATE (B-QUINOLINOL) (B-QUINOLINOL) NlOBlUM MINERAL CONCENTRATE WASTE IN V EN TOR.
- ARTHUR W. LAST KENT E MARQUARDSON titanium minerals.
Un t W8. 0
PROCESS OF CONCENTRATING COLUMBIUM MINERALS BY FROTH FLOTATION Arthur W. Last and Kent F. Marquardson, SaltLake City, Utah, assignors to Kennecott CopperCorporation, New York, N. Y., a corporation of New York Application October 10, 1957, Serial No. 689,435
14 Claims. (Cl. 209-166) This invention relates to the art of froth flotation for the selective recovery of specific minerals from their ores. It has particular reference to the recovery of columbium minerals from the ores in which they are found.
The metallic element niobium, or columbium as it is commonly called by metallurgists, has been known well over'a hundred years.
forms. 7 g n r There are vast deposits of columbium oresthat have been left 'unworked for the lack of any effective and economical process for separating the valuable'minerals from the ganguematerials with which they are associated in the natural ore deposits. Certain ores containing the mineral columbite are being worked in instances where separation of the columbite by gravity means,
It occurs in various mineral Another feature useful in minimizing reagent consumption is the reclaiming of the reagent-bearing solution from the final flotation pulp, and the use of same in preparing the initial flotation pulp for a subsequent run. This is advantageously done in connection with still another feature of the invention, namely, preliminary treatment of the ore for the elimination of various gangue ment for gangue elimination is dewatered. It is then re-pulped in recovered reagent-bearing solution prior to undergoing the significant froth flotation stage of the process.
" Further objects and features of the invention will become apparent as the description proceeds with respect to specific procedures and test results.
electrostatic means, or by magnetic means has proven economicallyfeasible. However, such separation procedures have not been economical in their application to ores containing other columbium minerals, such as py rochlore, perovskite, niocalite, betafite, etc.
No successful flotation process has to our-knowledge yet been reported for the selective flotation and recovery of colu'mbium minerals. There has hitherto been no known reagent capable of floating suchminerals on a selective basis. 7 V g n 7 We have found that columbium minerals may be effectively and economically floated from "gangue constituents of an ore by the use of a reagent selected from a. particular group of chemical compounds, serving as' a collector selective to such columbium minerals. The group of chemical compounds consists of a hydroxyquinoline, specifically, 8-quinolinol, commonly known as oxine, and mono-lower-alkyl-substituted 8-quinolinols.
While 8-quinolinol is well known as a chemical com pound, it is normally used in highly purified form in the chemical art as an analytical reagent. The only instances where 8-quinolinol has even been triedas a flotation reagent is in connection with certain academic investigations concerned with abstract flotationtheory. In such instances, the materials involved were merely artificial mixtures containing solely zinc, iron, tungsten, and Such experiments have evoked little interest, and have given no indication that the particular reagent has any eifectiveness as applied to columbium.
;In accordance with the present invention, the ore is finely ground in a manner customary in conventional flotation practice, and is subjected to agitation and aeration, as an aqueous pulp, in the presence of the particular reagent specified. The columbium minerals are effectively collected in the froth,- to yield a columbium concentrate.
A principal object of the present invention is to provide a froth flotation process whereby columbium minerals may be effectively recovered from their ores on a selective basis as respects other constituents'of such ores. Another object is to minimize reagent. consumption and expense,
Our work has shown that 8-quinolinol (C H NO) having the formula:
(8)2201; N 1 110 0 cn 2) 6 1 10 (5 21n on on is an active flotation reagent for columbium minerals when used either in the formof the'chernicallypure analytical reagent or in a crude form obtained as an impure reaction product of a known procedure.
This has been demonstrated by numerous laboratory v tests, typified by those set forth herebelow:
COMPARATIVE TESTS AS BETWEEN PURE AND 7 w CRUDE REAGENT a In this series of tests, respective 1,000 gram charges of a low grade, carbonatite type, columbium .ore from the province of Quebec, Canada, containing less than 0.6 percent columbium oxide (Ch o in the form of the minerals pyrochlore, perovskite, and others not yet definitely identified nor classified but believed to include A at least both niocalite and betafite, were ground to 90 percent minus 200 mesh. They were carefully deslimed, and were individually conditioned with the quantity of the reagent specified in the following tabulated test data and with 20 drops (0.6 gram) of burner oil, i. e. do-
. mestic fuel oil, for approximately one minute; They mixing 5 grains of o-nitrophenol, 8.3 grams of o-aminophenol, and 18 grams of glycerol in a 500 ml. flask, and
slowly adding 8.2 ml. of concentrated H the flask being fitted With a reflux condenser, and the mixture being boiled gently for five hours. Following cooling,
the resulting solution was dilutedto a volume of 250 m1.
e e -Reame wnce mt Weight, Chaos, Recov- Beagcnt percent percent ery, per- 7 cent (1) 2 g. o. P. 8-quinollnol ass 1. 49 90. s .(2) 60 ml. crude 8 guinolh1ol so1utlon 33.0 1.56 84.5 (3) 80 crude 8-qliiriolinolsolutionn 44.0 1. 37 93. 9 (4) 80 -ml. crude S-quinblinol solution I (reflux time 10 hours. 39. 7 l. 18 90.7
We have also found that reagent consumption can be reduced by treating the ore for removal .of various gangue minerals prior to flotation for recovery of the columbium minerals. A typical test is reported herebelow:
PRELIMINARY UPGRADING BY REMOVAL OF 1 GANGUE CONSTITUENTS This was a locked cyclic test, wherein, for each cycle, variousgangue constituents were removed by conventional techniques indicatedin the optional portion of the flow sheet of the accompanying drawing.
A charge of 4,000 grams .of the same carbonatite type, columbiurn ore was prepared for each cycle as in the foregoing tests, and was made into an aqueous pulp in accordance with conventional practice. Such aqueous pulp was subjected to flotation with a fatty acid collector reagent to remove calcite and apatite. The froth conccntrate was passed to Waste, and the tailings were subiected to, sulfideflotation utilizing a sulfonated petroleum oil'and a xanthate collector as reagents. The froth concentrate was passed to waste, and the tailings subjected to magnetic separation for the removal of magnetite.
The resulting upgraded ore pulp (from 0.6 percent Cb O to 2.36 percent Cb O was deslimed, and the deslimed pulp conditioned with 2 grams of C. P. 8-quinolinol and 1.5 grams of burner oil for flotation.
Agitation and aeration of the so conditioned pulp in a laboratory flotation machine resulted in a columbiumbearing froth, which was cleaned twice by further flotation of the same character. The cleaner tailings were added to the subsequent batch of ore pulp in accordance with'closed cycle practice. The metallurgical results were as follows:
Weight OM05, Dlstripercent percent bution, percent RECOVERY OF REAGENT-BEARING SOLUTION For this cyclic test, 1,000 gram batches of the same carbonatite type, eolumbium ore, prepared as in the foregoing tests, were deslimed .and upgraded by the aforedescribed mica and iron sulfide flotation and by removal of magnetite. In this instance, the pulp was not treated for removal of calcite andapatite.
The upgraded ore pulp was filtered, and the filter cake was used in the preparation of the aqueous pulp for the colu nbium flotation. The solution employed for this repulping operation was prepared initially from crude reagent obtained in the same manner as for the first series of tests, although, here, the reflux time was ten hours 4 (as in the touch o the iorego g t instead of five Six liters of solution were prepared from 150 ml. of the crude reagent. This supplied all dilution and wash water used during the flotation procedure, as well as the aqueous phase of the flotation pulp.
Agitation and aeration of the reagent-bearing pulp resulted in a columbium-bearing froth concentrate. The froth and tailings were separately filtered, and the respective filtrates were returned to the original solution. An additional 25 ml. of crude reagent was then added to the lt t O l, n the procedure was repeated.
In all, the procedure was carried out a total of six times. The recovery and grade of concentrates from the sixth cycle (after equilibrium was achieved) are tabulated as follows:
Rougher concentrate The difference in reagent consumption between the straight flotation process using 8-.quinolinol as a reagent and the more preferred practice of upgrading prior to flotation, coupled with recycling the liquid phase of the tailings and froth concentrate from the 8-quinolinol flotae tion, is well demonstrated by comparing Test No. 4 of the first series of tests with the last test above. It will be seen that comparable recovery was made in the latter instance with on y v25 n l. oi he crude reagent solution as compared with ml, for the former.
In the course of our work, many flotation tests were mad usin v r us conventio al eage ts n an ff rt t float col mbium m n ra sr; non f these yi ded e onom co y- A o in ly, n omparative tests as between the reagent here disclosed and other reagents are presented.
Our. tests have shown that the 8-quinolinol reagent, wh h n hemic l y p or crude rm, s effective in acid neutral, .or basic pulps. In such tests, however, recovery has fallen 01? considerably in the extremes of pH range. Accordingly, it is preferred that this flotation process be carried out with a near neutral pulp.
The 8-.quinolinol reagent has proven to have natural frothiug properties, which makes it unnecessary to add any other frothing reagent in many instances in which the process is used. It should be kept in mind, however, that the natural frothing properties may be supplemented wherever found desirable by addition of a conventional frothing agent, such as pine oil.
We have conducted tests on many difierent types of ores containing a variety of colurnbium minerals. These tests indicate that our process is effective on columbium minerals in general.
The following examples detail representative tests showing ratios of concentration of 1 to 12.1, 1 to 41.7,
and 1 to 9.5, respectively:
' EXAMPLE NO. 1
Two thousand grams of the carbonatite-type ore utilized in the previous tests were ground to approximately percent minus 200 mesh, deslimed, the iron sulfide minerals removed from the ore pulp by flotation using xanthate collector, and the magnetite removed magnetically. The ore pulp was then filtered, split into two equal parts, and each part was individually re-pulped in a laboratory flotation machine,.conditioned with 2.5 grams of 8-quinolinol, and afroth concentrate recovered. The tailings were combined for assay, and the froth concentrates were combined, conditioned with 0.5 gram of 8- quinolinol, and a froth concentrate recovered by flotation. The concentrate was then recleaned three times by flotation, using the solution recovered (by filtration) from the tailings of the previous step for dilution water.
Test results Weight, onto, Distri- Product percent percent butlon,
' percent- Concentrate 8. 24 6. 60 81. 84
CalculatedHeadlng 100.00 0.66 100.00
EXAJVEPLE NO. 2
One thousand grams of a pyrochlore-bearing granite from Nigeria were ground at 67 percent solids for twentythree minutes in a laboratory ball mill. The resultant pulp was deslimed, filtered, re/pulped ina laboratory flotation machine, conditioned with four grams of 8- quinolinol, and a froth concentrate removed. The froth concentrate was cleaned twice by flotation.
Weight, 0e20,, Distri- Product percent percent button,
percent Rougher Talllng 73. 83 0. 06 21. 93 1st Cleaner Taillng- 16. 21 0. 15. 25 2nd Cleaner Taillng.- 7. 56 0. 33 12.33 Concentrate 2. 40 4. 25 50. 49
Calculated Heading 100. 00 0. 100. 00
It will be obvious that various other elements, such as uranium, that are intimately associated with the columbium minerals will also be recovered by this process.
Comparative tests have been carried out, as follows:
Test No. 1 (8-quin0linol) Five hundred grams of a low grade carbonate type ore containing the columbium minerals Pyrochlore and Perovs kite and upgraded by removal of calcite and apatite, by desliming, and by removal of iron sulfide and magnetite were subjected to a batch flotation procedure involving flotation at pH 7.2 to 8.0 for ten minutes in the presence of two and one-half grams of 8-quinolinol. The rougher froth concentrate obtained was cleaned by reflotation, with the following results:
' Weight, 011205, Distri- Product percent percent butlon, percent Cleaner Concentrate 4. 74 10. 36 31.00 Cleaner Talllng 22.35 3.39 47.83 Rougher Taillng.. 72. 91 0. 46 21. 17
Calculated Feed 100. 00 1. 58 100. 00
Test No.2 (2- mefltyl-8-quinolin0l) 1 The procedure here was identical with that of the foregoing test, except 3.5 grams of Z-methyI-B-quinolinol (8- hydroxyquinaldine) wereused as the collector reagent; Results were as follows: r
' Weight, CD205, DlStli- Product percent percent button,
. percent Cleaner Concentrate 60 9. 21 30.82 Cleaner Talllng 24. 68 4. 07 40. 90 Rougher Tailing 68. 72 0.53 18. 28
Calculated Feed 100. 00 1. 98 100. 00
Test No. 3 (4-methyl-8- quinolinol)' The procedure here was identical with the foregoing tests, except 2.0 grams of4-methyl-8-quinolinol were used as the collector reagent. Results were as follows:
7 Weight, 05.0,, Distri- Product percent percent butlon,
percent Recleaner Concentrate 3. 18 19. 3 34. 70 Recleaner Telling 7. 01 5. 24 20. 77 Cleaner Talllng 43. 10 l. 60 38. 99 Rougher Talllng 46. 71 0. 21 5. 54
Test N0. 4 (6-methyl-8-quirtolinol) The procedure here was identical with the foregoing tests, except 2.0 grams of 6-methyl-8-quinolinol were used as the collector reagent. Results were as follows:
Of the several reagents used in the above series of tests, only S-quinolinol is readily available. It was possible to purchase the reagent for Test No. 2 from Eastman Kodak Company, but the reagents for Tests No. 3 and 4 were synthesized in the laboratory.
This application constitutes a continuation-in-part of our copending application Serial Number 612,849, filed Sept. 28, 1956, entitled Process of Concentrating Niobium Minerals by Froth Flotation, which has been found to be allowable but which has been abandoned in favor of the present application.
We claim:
1. In a process of froth flotation for the separation of columbium minerals from other constituents of a columbium ore, the steps of agitating and aerating an aqueous pulp containing said columbium ore and 8- quinolinol, the latter serving as a collector reagent selective to columbium minerals; and recovering the resulting froth as a columbium concentrate.
2. The process of claim 1, wherein the said steps are preceded by pro-concentration treatment of an aqueous pulp of the ore.
3. The process of claim 2, wherein the procedure is carried out on a cyclic basis, and, following the said steps of each cycle, at least the tailings are treated for recovery of their reagent-bearing liquid phase; wherein the upgraded pulp is treated for removal of its liquid phase; and wherein the solid phase of said upgraded pulp is re-pulped with the recovered reagent-bearing liquid phase.
4. The process of claim 3, wherein the 8-quinolinol is an impure reaction product.
5, The process of claim 1,, wherein 'alsocontains-a neutral petroleum oil. H 7 v 6. The process of claim 1, wherein the S-quinolinol isv an impure reaction product.
'7. The process of claim 1, wherein at least the tailings resulting from the said steps are'treated for recovery of their reagent-bearing liquid phase; and wherein the said'liquid phase is used in pulping additional ore for said process. a
I 8. The process of claim 1, wherein the said steps are preceded by flotation of sulfide minerals from an aqueous pulp of the ore, for upgrading said ore.
9. In a process of froth flotation for the separation of columbium minerals from other constituents of a columbium ore, the steps of agitating and aerating an aqueous pulp containing said columbium ore and a collector reagent selected from'the group consisting of 8- quinolinol and mono-lower-alkyl-substituted 8-quinolinols; and recovering the resulting froth as a columbium concentrate.
10. The process of claim 9, wherein the said steps are preceded by pre-concentration treatment of an aqueous pulp of the ore.
the aqueous pulp r 8 i '11. .The process of clairnlO, wherein the procedure is carried out on acyclic basis, and, following the said steps of each cycle, at least the tailings are treated for recovery of their reagent-bearingliquid phase; wherein 'the upgraded pulp is treated for removal ofitsliquid i in the said liquid phase is used in pulping additional ore for said process.
14. The process of claim 9, wherein the said steps are preceded by flotation of sulfide minerals from an aqueous pulp of the ore, for upgrading said ore.
References Cited in the file of this patent Oxine and Its Derivatives, Hollingshead, vol. II, 594- 596, 1954.
Claims (1)
1. IN A PROCESS OF FROTH FLOTATION FOR THE SEPARATION COLUMBIUM MINERALS FROM OTHER CONSTITUENTS OF A COLUMBIUM ORE, THE STEPS OF AGITATING AND AERATING AN AQUEOUS PULP CONTAINING SAID COLUMBIUM ORE AND 8QUINOLINOL, THE LATTER SERVING AS A COLLECTOR REAGENT SELECTIVE TO COLUMBIUM MINERALS; AND RECOVERING THE RESULTING FROTH AS A COLUMBIUM CONCENTRATE.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB37059/56A GB798768A (en) | 1956-09-28 | 1956-12-04 | Process of concentrating niobium minerals by froth flotation |
US689435A US2875896A (en) | 1957-10-10 | 1957-10-10 | Process of concentrating columbium minerals by froth flotation |
GB18196/58A GB826827A (en) | 1957-10-10 | 1958-06-06 | Process of concentrating niobium minerals by froth flotation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US689435A US2875896A (en) | 1957-10-10 | 1957-10-10 | Process of concentrating columbium minerals by froth flotation |
Publications (1)
Publication Number | Publication Date |
---|---|
US2875896A true US2875896A (en) | 1959-03-03 |
Family
ID=24768454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US689435A Expired - Lifetime US2875896A (en) | 1956-09-28 | 1957-10-10 | Process of concentrating columbium minerals by froth flotation |
Country Status (2)
Country | Link |
---|---|
US (1) | US2875896A (en) |
GB (1) | GB826827A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2951585A (en) * | 1958-09-08 | 1960-09-06 | Burks Herbert George | Separation of pyrochlore from calcite, apatite and silica |
US2959281A (en) * | 1958-12-31 | 1960-11-08 | Technical Managers Inc | Flotation of niobium-bearing minerals |
US2975895A (en) * | 1958-12-24 | 1961-03-21 | Nova Beaucage Mines Ltd | Flotation process |
US3014585A (en) * | 1959-06-18 | 1961-12-26 | Harvey L Noblitt | Flotation process for concentrating niobium-bearing minerals |
US3430762A (en) * | 1966-11-28 | 1969-03-04 | David Weston | Simultaneous flotation of silica phosphates and carbonate minerals |
US3910836A (en) * | 1972-01-29 | 1975-10-07 | Soquem | Pyrochlore flotation |
US4178235A (en) * | 1978-06-30 | 1979-12-11 | Wilson James A | Flotation recovery of pyrochlore |
US4192738A (en) * | 1978-10-23 | 1980-03-11 | The United States Of America As Represented By The Secretary Of The Interior | Process for scavenging iron from tailings produced by flotation beneficiation and for increasing iron ore recovery |
US4342648A (en) * | 1981-05-05 | 1982-08-03 | Les Services Tmg Inc. | Direct flotation of pyrochlore |
US4466886A (en) * | 1982-09-28 | 1984-08-21 | Vojislav Petrovich | Froth flotation method for recovering minerals |
WO2003066915A1 (en) * | 2002-02-08 | 2003-08-14 | Cabot Corporation | Metal recovery process |
WO2005113152A1 (en) * | 2004-05-10 | 2005-12-01 | Clariant Produkte (Deutschland) Gmbh | Collector for sulfidic ores |
WO2024164587A1 (en) * | 2023-02-09 | 2024-08-15 | 广东省科学院资源利用与稀土开发研究所 | Beneficiation method for recovering pyrochlore from high-silicon high-calcium carbonatite-type niobium ore |
-
1957
- 1957-10-10 US US689435A patent/US2875896A/en not_active Expired - Lifetime
-
1958
- 1958-06-06 GB GB18196/58A patent/GB826827A/en not_active Expired
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2951585A (en) * | 1958-09-08 | 1960-09-06 | Burks Herbert George | Separation of pyrochlore from calcite, apatite and silica |
US2975895A (en) * | 1958-12-24 | 1961-03-21 | Nova Beaucage Mines Ltd | Flotation process |
US2959281A (en) * | 1958-12-31 | 1960-11-08 | Technical Managers Inc | Flotation of niobium-bearing minerals |
US3014585A (en) * | 1959-06-18 | 1961-12-26 | Harvey L Noblitt | Flotation process for concentrating niobium-bearing minerals |
US3430762A (en) * | 1966-11-28 | 1969-03-04 | David Weston | Simultaneous flotation of silica phosphates and carbonate minerals |
US3910836A (en) * | 1972-01-29 | 1975-10-07 | Soquem | Pyrochlore flotation |
US4178235A (en) * | 1978-06-30 | 1979-12-11 | Wilson James A | Flotation recovery of pyrochlore |
US4192738A (en) * | 1978-10-23 | 1980-03-11 | The United States Of America As Represented By The Secretary Of The Interior | Process for scavenging iron from tailings produced by flotation beneficiation and for increasing iron ore recovery |
US4342648A (en) * | 1981-05-05 | 1982-08-03 | Les Services Tmg Inc. | Direct flotation of pyrochlore |
US4466886A (en) * | 1982-09-28 | 1984-08-21 | Vojislav Petrovich | Froth flotation method for recovering minerals |
WO2003066915A1 (en) * | 2002-02-08 | 2003-08-14 | Cabot Corporation | Metal recovery process |
US20030152503A1 (en) * | 2002-02-08 | 2003-08-14 | Claude Deveau | Metal recovery process |
US6953120B2 (en) | 2002-02-08 | 2005-10-11 | Cabot Corporation | Method of recovering metal and/or oxide thereof in a slurry and tailings obtained from said method |
WO2005113152A1 (en) * | 2004-05-10 | 2005-12-01 | Clariant Produkte (Deutschland) Gmbh | Collector for sulfidic ores |
US20070221878A1 (en) * | 2004-05-10 | 2007-09-27 | Heinrich Hesse | Collector for Sulfidic Ores |
US7695634B2 (en) | 2004-05-10 | 2010-04-13 | Clariant Produkte (Deutschland) Gmbh | Collector for sulfidic ores |
WO2024164587A1 (en) * | 2023-02-09 | 2024-08-15 | 广东省科学院资源利用与稀土开发研究所 | Beneficiation method for recovering pyrochlore from high-silicon high-calcium carbonatite-type niobium ore |
Also Published As
Publication number | Publication date |
---|---|
GB826827A (en) | 1960-01-20 |
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