US2385819A - Beneficiation of beryllium ores - Google Patents
Beneficiation of beryllium ores Download PDFInfo
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- US2385819A US2385819A US502081A US50208143A US2385819A US 2385819 A US2385819 A US 2385819A US 502081 A US502081 A US 502081A US 50208143 A US50208143 A US 50208143A US 2385819 A US2385819 A US 2385819A
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- Prior art keywords
- ore
- beryl
- percent
- pulp
- beryllium
- Prior art date
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- 229910052790 beryllium Inorganic materials 0.000 title description 12
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 title description 12
- 229910052614 beryl Inorganic materials 0.000 description 29
- 239000012141 concentrate Substances 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 150000004665 fatty acids Chemical class 0.000 description 11
- 239000003513 alkali Substances 0.000 description 9
- 238000005188 flotation Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- NJJFVOQXYCEZLO-UHFFFAOYSA-N dialuminum;triberyllium;dioxido(oxo)silane Chemical compound [Be+2].[Be+2].[Be+2].[Al+3].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O NJJFVOQXYCEZLO-UHFFFAOYSA-N 0.000 description 7
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 5
- 244000060011 Cocos nucifera Species 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 230000003750 conditioning effect Effects 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000010433 feldspar Substances 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- MHDPNLWXRXCIIL-UHFFFAOYSA-N 1-(2-hydroxyethoxy)tetradecan-2-ol;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCC(O)COCCO MHDPNLWXRXCIIL-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CNLWCVNCHLKFHK-UHFFFAOYSA-N aluminum;lithium;dioxido(oxo)silane Chemical compound [Li+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O CNLWCVNCHLKFHK-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 3
- 238000009291 froth flotation Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 229910052952 pyrrhotite Inorganic materials 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910052642 spodumene Inorganic materials 0.000 description 3
- 229910052613 tourmaline Inorganic materials 0.000 description 3
- 239000011032 tourmaline Substances 0.000 description 3
- 229940070527 tourmaline Drugs 0.000 description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 239000002223 garnet Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910052683 pyrite Inorganic materials 0.000 description 2
- 239000011028 pyrite Substances 0.000 description 2
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 1
- CKKQNAYCAVMZGX-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl hydrogen sulfate Chemical compound OCCOCCOS(O)(=O)=O CKKQNAYCAVMZGX-UHFFFAOYSA-N 0.000 description 1
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000375392 Tana Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- DLHONNLASJQAHX-UHFFFAOYSA-N aluminum;potassium;oxygen(2-);silicon(4+) Chemical group [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Si+4].[Si+4].[Si+4].[K+] DLHONNLASJQAHX-UHFFFAOYSA-N 0.000 description 1
- 229910001767 beryllium mineral Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052626 biotite Chemical group 0.000 description 1
- 229910001602 chrysoberyl Inorganic materials 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- YGANSGVIUGARFR-UHFFFAOYSA-N dipotassium dioxosilane oxo(oxoalumanyloxy)alumane oxygen(2-) Chemical group [O--].[K+].[K+].O=[Si]=O.O=[Al]O[Al]=O YGANSGVIUGARFR-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000003760 hair shine Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000002699 waste material 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
- B03D1/02—Froth-flotation processes
-
- 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
- B03D1/08—Subsequent treatment of concentrated product
- B03D1/085—Subsequent treatment of concentrated product of the feed, e.g. conditioning, de-sliming
Definitions
- caustic alkali such as caustic soda
- the blunging step appears to condition the ore for'subsequent treatment. After blunging, the pH of the resulting pulp is adjusted to lie within the neutral to slightly alkaline range,
- v such as pH 6 to pH 9, and preferably within the range pH 6.5 to pH 8.
- the adjustment of pH is made by neutralizing with a hydroxy aliphatic acid, such as glycolic acid, tartaric acid, citric acid
- a hydroxy aliphatic acid such as glycolic acid, tartaric acid, citric acid
- Another object is to product beryl concentrates I from low grade deposits to yield beryl concentrates of a marketable grade. Other objects will be apparent or will hereinafter appear.
- b'eryl can be concentrated from pegmatitic gangue's of extremely variable composition by conditioning the finelysround de-slimed ore with a strong alkali, thereafter the pH is adjusted to approximately the range pH 6 to pH 9, and by a flotation operation in the presence of a fatty acid collector and a frothing agent. It appears that the success of the operation is in some measure related to the alkali conditioning step followed by at least partial neutralization, since the high emciency of the method appears to be influenced by this sequence of operations.
- Suitable beryllium ores adapted for use in the present process include beryl when found in gangues of extremely variable composition. such as for example feldspar, clevelandite, .quartz, mica, tourmaline, garnet, pyrrhotite, spodumene, zircon, pyrite, cassiterite, lithiophiiite-and Durpurite.
- Other beryllium ores may also be adapted for concentration in the present invention, such ores as chrysoberyl, helvite and phenaeite being exemplary, but the preferred beryllium ore for treatment is an ore containing beryl itself.
- the ore is preferably stage-ground to minus 65 mesh (standard Tyler screen) and de-slimed by washing or other known means. Thereafter the ore is blunged for preferably 10 toBO minutes in water containing per ton of ore from 1 lb. to 5 acids of from 8 to 18 carbon atoms, for example, caprylic acid, lauric acid, oleic acid or stearic acid and preferably with a mixture of naturally occurringfatty acids obtained from coconut oil.
- Suitable frothing agents include lower alkyl glycolic esters, the mixture of branched chain higher synthetic alcohols produced in the methanol synthesis, and preferably the synthetic frothing agent known as Emulsol X-l, believed to be the ammonium salt of lauryl diethylene glycol sulfate. 1
- the frothing agent can be employed in proportions of about 0.01 to 1.0 lb. per ton of ore and is preferably employed in proportions of about 0.05
- the fatty acid reagent is employed in the proportions of 0.1 to 1 lb. per 'ton, and preferably from about 0.1 to 0.5 pound per ton of ore being treated.
- the flotation step can be carried out in any of the ordinary flotation apparatus, and the core is preferably conditioned by agitating with the flotation reagents from 5 to 25 minutes before the air feed is begun.
- a sample is stage-ground to pass a 20-mesh screen, being careful to avoid the production of flnes.
- the minus 20- mesh sample is further ground in a ball mill with an equal amount of water to minus mesh size.
- the ground pulp is then de-slimed by admixing with 10 parts of water to each part of ore by weight. stirring and decanting the slimes.
- the resulting sands are agitated with an equal weight of water and from 1 to 5 lbs. of caustic soda per ton of ore. The agitation is continued for about 10 to 30 minutes, the charge then diluted with 10 parts of water per part of ore and the operation repeated until the pH lies within the preferred range of pH 6.5 to pH 8.
- the pulp is diluted to 20% solids with water and notation reagents added in the proportion of. p r ton of ore, preferably 1 lb. of coconut fatty acid and 0.6 lb. of "Emulsol .X-1.”"'i ⁇ fter a 5 minute conditioning period the air is turned on in the flOtBr tion machine and the beryl concentrate recovered as froth over-flow.
- the flotation is carried out to produce a rougher concentrate, which is then passed on to a cleaner cell to'produce a finished concentrate and middlings which are returned to the feed.
- one stage of flotation is carried on for recovery and the sec nd stage for grade.
- EXAMPLE 1 Beryllium ore from the Black Mountain deposit near Rumford, Maine, which assayed 1.7% BeO (or approximately 12% beryl) and which also contained feldspar (clevelandite), quartz and mica with minor amounts of tourmaline, "garnet, pyrrhotite, spodumene, zircon, pyrite, cassiterite. lithiophilite and purpurite was treated in accordance with the foregoing outlined procedure.
- Tana 2.Rl:sm.'rs or Hora-non TIST on Wuxs QumxOu Analysis Percent Weig t Product percent; ottotal Pounds per ton of ore Rougher Reagents Blunge Test; on the Gotta-Walden ore yielded higher grade concentrates than either the Black Mountain or Weeks Quarry ores. Results shown in Table 3 'indicate'avrecovery of 71.4 percent of the beryl with concentrates assaying 94 percent beryl or 13.2 percent BeO.
- I EXAMPLE 4 The ore from the Weeks Quarry described in I Example 2 was continuousl'ytreated by crushing in a jaw-crusher. then passing through rolls to pass a B-mesh screen and thereafter separating the mica by screening I screen. The ore then had the following characteristics: TAaL:-4.--Rlsm.'rs or Causnmo mo Scunmw Wuxs Quasar 0a:
- theprocedure is especially suitable for concentrating beryl from pegmatitic gangue materials, it is applicable to other beryllium ores as well.
- a process of concentrating beryl from its ores which comprises commlnuting the ore tosuitable particle size, pre-treating the comminuted ore by agitating it in a pulp containing from one to five pounds per ton of ore of caustic alkali, then washing the alkali away from the ore, then conditioning the thus alkali-treated and washed ore by agitating it in'a pulp containing fatty acid and the ammonium salt of lauryl diethylene glycol sulfate, and subjecting the thusconditioned pulp of beryl ore to froth-flotation toseparate in the froth a concentrate of beryl.
- a process of concentrating beryl from its ores which, comprises commlnuting said ore to at least minus 65-mesh particle size, pre-treating the comminuted ore by agitating it in a pulp containing from 1 to 5 lbs. of caustic soda per ton of ore, then washing the alkali away from the ore, then conditioning the thus-alkali-treated and washed ore by agitating for at least ininutes in a pulp containing flotation reagents consisting of coconut oil fatty acids and the ammonium salt of iauryl diethylene glycol sulfate and subjecting the thus-conditioned pulp of beryl ore to froth-flotation to separate in the froth a concentrate of beryl.
- a process for the beneflciation of beryl ores which comprises blunging a finely-ground, deslimed beryl ore admixed with a pegmatitic gangue in aqueous caustic soda solution containing from 1 to 5 lbs. caustic soda per ton of ore,
Landscapes
- Paper (AREA)
Description
was on. 2, 945
UNITED .STATES PATENT OFFICE I nanmcrsnorfzi fii znrnuorr ones as aches.
m Md the United States, as represented by the Secretary of the Interior No Drawing.
6Ciaims.
' centration of beryl from pegmatitic gangues.
It is an object of this invention to beneflciate beryllium ores. Another object is to concentrate beryl from ores containing pegmatitic gangues.
Application September 13, 1943, Serial No. 502,081
(Granted under the act of March 3, 1883, as amended April 30, 1928; 370 0. G. 357) lbs. of caustic alkali, such as caustic soda, and
the like. The blunging step appears to condition the ore for'subsequent treatment. After blunging, the pH of the resulting pulp is adjusted to lie within the neutral to slightly alkaline range,
v such as pH 6 to pH 9, and preferably within the range pH 6.5 to pH 8. The adjustment of pH is made by neutralizing with a hydroxy aliphatic acid, such as glycolic acid, tartaric acid, citric acid Another object is to product beryl concentrates I from low grade deposits to yield beryl concentrates of a marketable grade. Other objects will be apparent or will hereinafter appear.
and preferably lactic acid, or preferably by washing the ore with water until the pH lies within the desired range. The ore-pulp is then subjected to a froth flotation treatment in the presence of v a frothing agent and a fatty acid, such as fatty These objects are accomplished in accordance with this invention by blunging a finely-ground, de-slimed beryl ore in admixture with aqueous a1- kali, thereafter adjusting the pH of the mixture to the approximately neutral range, then agitating and aerating the mixture in the presence of a frothing agent and collector comprising a fatty acid containing from- 8 to 18 carbon atoms, and
separating a froth containing the beryl concentrate.
It has been discovered that b'eryl can be concentrated from pegmatitic gangue's of extremely variable composition by conditioning the finelysround de-slimed ore with a strong alkali, thereafter the pH is adjusted to approximately the range pH 6 to pH 9, and by a flotation operation in the presence of a fatty acid collector and a frothing agent. It appears that the success of the operation is in some measure related to the alkali conditioning step followed by at least partial neutralization, since the high emciency of the method appears to be influenced by this sequence of operations.
Suitable beryllium ores adapted for use in the present process include beryl when found in gangues of extremely variable composition. such as for example feldspar, clevelandite, .quartz, mica, tourmaline, garnet, pyrrhotite, spodumene, zircon, pyrite, cassiterite, lithiophiiite-and Durpurite. Other beryllium ores may also be adapted for concentration in the present invention, such ores as chrysoberyl, helvite and phenaeite being exemplary, but the preferred beryllium ore for treatment is an ore containing beryl itself.
The ore is preferably stage-ground to minus 65 mesh (standard Tyler screen) and de-slimed by washing or other known means. Thereafter the ore is blunged for preferably 10 toBO minutes in water containing per ton of ore from 1 lb. to 5 acids of from 8 to 18 carbon atoms, for example, caprylic acid, lauric acid, oleic acid or stearic acid and preferably with a mixture of naturally occurringfatty acids obtained from coconut oil. Suitable frothing agents include lower alkyl glycolic esters, the mixture of branched chain higher synthetic alcohols produced in the methanol synthesis, and preferably the synthetic frothing agent known as Emulsol X-l, believed to be the ammonium salt of lauryl diethylene glycol sulfate. 1
The frothing agent can be employed in proportions of about 0.01 to 1.0 lb. per ton of ore and is preferably employed in proportions of about 0.05
' to 0.5 pound per ton of ore.
The fatty acid reagent is employed in the proportions of 0.1 to 1 lb. per 'ton, and preferably from about 0.1 to 0.5 pound per ton of ore being treated. The flotation step can be carried out in any of the ordinary flotation apparatus, and the core is preferably conditioned by agitating with the flotation reagents from 5 to 25 minutes before the air feed is begun.
In a typical operation, a sample is stage-ground to pass a 20-mesh screen, being careful to avoid the production of flnes. Thereafter the minus 20- mesh sample is further ground in a ball mill with an equal amount of water to minus mesh size. The ground pulp is then de-slimed by admixing with 10 parts of water to each part of ore by weight. stirring and decanting the slimes. The resulting sands are agitated with an equal weight of water and from 1 to 5 lbs. of caustic soda per ton of ore. The agitation is continued for about 10 to 30 minutes, the charge then diluted with 10 parts of water per part of ore and the operation repeated until the pH lies within the preferred range of pH 6.5 to pH 8. Thereafter the pulp is diluted to 20% solids with water and notation reagents added in the proportion of. p r ton of ore, preferably 1 lb. of coconut fatty acid and 0.6 lb. of "Emulsol .X-1.""'i \fter a 5 minute conditioning period the air is turned on in the flOtBr tion machine and the beryl concentrate recovered as froth over-flow. Preferably the flotation is carried out to produce a rougher concentrate, which is then passed on to a cleaner cell to'produce a finished concentrate and middlings which are returned to the feed. Thus, one stage of flotation is carried on for recovery and the sec nd stage for grade. I
' The following examples illustrate how the invention may be carried out but it is not limited thereto:
EXAMPLE 1 Beryllium ore from the Black Mountain deposit near Rumford, Maine, which assayed 1.7% BeO (or approximately 12% beryl) and which also contained feldspar (clevelandite), quartz and mica with minor amounts of tourmaline, "garnet, pyrrhotite, spodumene, zircon, pyrite, cassiterite. lithiophilite and purpurite was treated in accordance with the foregoing outlined procedure.
The results are tabulated as follows:
Tans: 1 .Rr:sm.'rs or notation-Tsar on BLACK Mouxram 0a:
The results shown in Table 1 indicate a recovery of 60 percent of the total beryl with concentrates containing 75.7 percent beryl or 10.60 percent BeO. The greatest loss was in the slimes portion of the ore which contained 21.9 percent of the total beryl. .Petrographic examination of the concentrates showed that the concentrates contain, beside beryl, mainly feldspar and mica, and minor amounts of tourmaline, spodumene,
net, quartz, and pyrrhotite.
- A beryl ore from the Weeks Quarry, East Wakefield, New Hampshire; which assayed 1.4% BeO (approximately beryl) and in which the feldspar was in the orthoclase' form, was similarly Pounds per ton of ore Reagents Blungs s 2g Bougher 1 5.0 Y Ooconuti' acid. 0.8 Emuisolx- 0.4 I Tims,minutss-- so 5 a a s a Results obtained from the Weeks Quarry ore were somewhat better than those on the Black Mountain ore. Table 2 shows a recovery of 74.7 percent of the total beryl with concentrates assaying 87 percent beryl, or 12.2-percent BeO.
Loss of beryl in the slimes amounted to 21.0 percent. i
EXAMPLE 3 A beryl ore from the Gotta-Walden property, Portland, Connecticut, which assayed 0.55% BeO (3.9% beryl) and which contained considerable 'mica'in the muscovite and biotite forms was treated in accordance with the above-outlined procedure- The results 'of the treatment are as follows:
TABLI' Zia-Resume or Fnounou Tlsr on Gu a-Wannm 0a:
' I /i I Analysis Percent Weight Product percent of total Cleaner cones 4. 1 9i. 0 71. 4 Cleaner -0.'! 5.0 0.0 Rougher tails.-- 71. 1 0. 6 as "'Blimes 24. 1 4. a 21.4 Composite head 100. 0 5. 4 100.0
treated in accordance with the above outlined procedure; The resultsare tabulated as follows:
Tana: 2.Rl:sm.'rs or Hora-non TIST on Wuxs QumxOu Analysis Percent Weig t Product percent; ottotal Pounds per ton of ore Rougher Reagents Blunge Test; on the Gotta-Walden ore yielded higher grade concentrates than either the Black Mountain or Weeks Quarry ores. Results shown in Table 3 'indicate'avrecovery of 71.4 percent of the beryl with concentrates assaying 94 percent beryl or 13.2 percent BeO.
I EXAMPLE 4 The ore from the Weeks Quarry described in I Example 2 was continuousl'ytreated by crushing in a jaw-crusher. then passing through rolls to pass a B-mesh screen and thereafter separating the mica by screening I screen. The ore then had the following characteristics: TAaL:-4.--Rlsm.'rs or Causnmo mo Scunmw Wuxs Quasar 0a:
- Percen t a Size 1 Weight inesl'r pounds #3 11 B01 miss. I 4s &3 MillieeiL. oea 0&1 Composite.-- 708 100.0,
. After screening to remove excess mice, the ore was ground in a ball-mill in closed circuit with anAkins type classifier. After-grinding the ore de-slimed in a- Dorr Simplex classifier to p duce a sized feed and shines having the 1'01- 1 wingcharacteristics:
through a vibratins Tssu: 5.4mm Ammrsrs or Prsor Pssnr fitness Percent of Size, mesh total weight I Compcsitei to waste and the raked product to a Denver conditioner. The coconut fatty acid and the Emulsol X-l was fed to the conditioner at the rate of 1 lb. of fatty acid and 0.5 lb. of Emuisol X-l." per ton of ore. From the conditioner, the pulp flowed to the rougher cell of a bank of six flotation cells (Denver Equipment Co. type), froth from the rougher cell was returned to the cleaner cell and tailings from the rougher cellto three scavenger cells. Froth from the first cleaner cell wasfurther cleaned in another cleaner cell and the tailings from both cleaner cells were returned as middlings to the rougher cell feed. The pH in the rougher cell was'7.2 and the pulp density therein was 1.13. A recovery of 69.5% of the beryl ore was made with concentrates containing 70.5% beryl. The results of the nm are tabulated as follows:
Tests 6.'--RIULTS or Pnor PLAN! Fso'rs'rron Tasr Percent of total beryl 'Iailings' Composite heads 1 From the foregoing it is apparent that a desirable procedure has been provided for concentrating beryl from its ores, to yield a concentrate containing at least 0% by weight beryllium calculated as 3120. 1
Although theprocedure is especially suitable for concentrating beryl from pegmatitic gangue materials, it is applicable to other beryllium ores as well.
Although in the examples. the 'slimes were 2. A process of concentrating beryl from its ores which comprises commlnuting the ore tosuitable particle size, pre-treating the comminuted ore by agitating it in a pulp containing from one to five pounds per ton of ore of caustic alkali, then washing the alkali away from the ore, then conditioning the thus alkali-treated and washed ore by agitating it in'a pulp containing fatty acid and the ammonium salt of lauryl diethylene glycol sulfate, and subjecting the thusconditioned pulp of beryl ore to froth-flotation toseparate in the froth a concentrate of beryl.
3. A process of concentrating beryl from its ores which, comprises commlnuting said ore to at least minus 65-mesh particle size, pre-treating the comminuted ore by agitating it in a pulp containing from 1 to 5 lbs. of caustic soda per ton of ore, then washing the alkali away from the ore, then conditioning the thus-alkali-treated and washed ore by agitating for at least ininutes in a pulp containing flotation reagents consisting of coconut oil fatty acids and the ammonium salt of iauryl diethylene glycol sulfate and subjecting the thus-conditioned pulp of beryl ore to froth-flotation to separate in the froth a concentrate of beryl.
4. A process for the beneflciation of beryl ores which comprises blunging a finely-ground, deslimed beryl ore admixed with a pegmatitic gangue in aqueous caustic soda solution containing from 1 to 5 lbs. caustic soda per ton of ore,
- thereafter adjusting the pH of the mixture to discarded, they can likewise be treated to recover to approximate neutrality, then andv the range pH6 to pH9, then agitating and aerating the mixture in the presence of a frothing agent in the'amount of 0.05 to 0.5 lb. per ton of ore and about 0.1 to 1.0 lb. of coconut fatty acid ore, plunging the deslime'd ore from 10 to 30 minutes with an equal weight of water containing from one to five pounds caustic soda per ton of ore, then diluting with excess water and decanting the solution until the pH of the pulp is between seven and eight. thereafter subjecting the pulp to agitation and aeration in the presence of, per ton of ore, about one pound of coconut fatty acids and about 0.5 pound of the ammonium salt of lauryl diethylene glycol sulfate, and separating I a froth containing on the dry basis at least 9% by weight beryllium calculated as the oxide.
.6, In a process for the production .of'a highgrade beryllium concentrate involving the flotation of a beryllium mineral, the steps which comprise pretreating a comminuted de-slimed beryllium ore with from one to five poundsper ton of ore of a strong alkali. adiustins the pulp pH to the neutral to slightly alkaline range, then agitating and aerating the pulp in the presence of coconut fatty acid and the ammonium salt of lauryl diethylene'glycol sulfate, and separatinl a froth concentrate containing at least 9% by weight beryllium calculated as the oxide.
- FRANK D. LAMB.
LLOYD EARNING,
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US502081A US2385819A (en) | 1943-09-13 | 1943-09-13 | Beneficiation of beryllium ores |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US502081A US2385819A (en) | 1943-09-13 | 1943-09-13 | Beneficiation of beryllium ores |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2385819A true US2385819A (en) | 1945-10-02 |
Family
ID=23996251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US502081A Expired - Lifetime US2385819A (en) | 1943-09-13 | 1943-09-13 | Beneficiation of beryllium ores |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2385819A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3028008A (en) * | 1960-07-27 | 1962-04-03 | James S Browning | Separation of spodumene and beryl by flotation |
| US3078997A (en) * | 1961-02-24 | 1963-02-26 | Havens Richard | Flotation process for concentration of phenacite and bertrandite |
| US3430765A (en) * | 1965-08-11 | 1969-03-04 | Allied Chem | Beneficiation of fluorspar ores |
| US4735710A (en) * | 1986-09-05 | 1988-04-05 | Falconbridge Limited | Beryllium flotation process |
| US5057209A (en) * | 1989-04-11 | 1991-10-15 | The Dow Chemical Company | Depression of the flotation of silica or siliceous gangue in mineral flotation |
| US5124028A (en) * | 1990-06-28 | 1992-06-23 | The Dow Chemical Company | Froth flotation of silica or siliceous gangue |
| US5131600A (en) * | 1989-02-13 | 1992-07-21 | The Dow Chemical Company | Alkanol amine grinding aids |
-
1943
- 1943-09-13 US US502081A patent/US2385819A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3028008A (en) * | 1960-07-27 | 1962-04-03 | James S Browning | Separation of spodumene and beryl by flotation |
| US3078997A (en) * | 1961-02-24 | 1963-02-26 | Havens Richard | Flotation process for concentration of phenacite and bertrandite |
| US3430765A (en) * | 1965-08-11 | 1969-03-04 | Allied Chem | Beneficiation of fluorspar ores |
| US4735710A (en) * | 1986-09-05 | 1988-04-05 | Falconbridge Limited | Beryllium flotation process |
| US5131600A (en) * | 1989-02-13 | 1992-07-21 | The Dow Chemical Company | Alkanol amine grinding aids |
| US5057209A (en) * | 1989-04-11 | 1991-10-15 | The Dow Chemical Company | Depression of the flotation of silica or siliceous gangue in mineral flotation |
| US5124028A (en) * | 1990-06-28 | 1992-06-23 | The Dow Chemical Company | Froth flotation of silica or siliceous gangue |
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