USRE19192E - Process of flotation - Google Patents
Process of flotation Download PDFInfo
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- USRE19192E USRE19192E US19192DE USRE19192E US RE19192 E USRE19192 E US RE19192E US 19192D E US19192D E US 19192DE US RE19192 E USRE19192 E US RE19192E
- Authority
- US
- United States
- Prior art keywords
- flotation
- phosphorus
- reaction
- compounds
- substances
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 238000005188 flotation Methods 0.000 title description 22
- 238000000034 method Methods 0.000 title description 9
- 239000000126 substance Substances 0.000 description 21
- 229910052698 phosphorus Inorganic materials 0.000 description 16
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 15
- 239000011574 phosphorus Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 13
- -1 alkali metal salts Chemical class 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000007795 chemical reaction product Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- 239000003513 alkali Substances 0.000 description 7
- 125000004429 atom Chemical group 0.000 description 7
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 238000009291 froth flotation Methods 0.000 description 5
- 150000004707 phenolate Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000008396 flotation agent Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical class S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 description 3
- 125000004437 phosphorous atom Chemical group 0.000 description 3
- 239000011269 tar Substances 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- OTYNBGDFCPCPOU-UHFFFAOYSA-N phosphane sulfane Chemical compound S.P[H] OTYNBGDFCPCPOU-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZRKMQKLGEQPLNS-UHFFFAOYSA-N 1-Pentanethiol Chemical compound CCCCCS ZRKMQKLGEQPLNS-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical class [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 241000755093 Gaidropsarus vulgaris Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- 229940051043 cresylate Drugs 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XDEZOLVDJWWXRG-UHFFFAOYSA-N methylenedioxycathinone Chemical group CC(N)C(=O)C1=CC=C2OCOC2=C1 XDEZOLVDJWWXRG-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000011297 pine tar Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- ZGJADVGJIVEEGF-UHFFFAOYSA-M potassium;phenoxide Chemical compound [K+].[O-]C1=CC=CC=C1 ZGJADVGJIVEEGF-UHFFFAOYSA-M 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052569 sulfide mineral Inorganic materials 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/014—Organic compounds containing phosphorus
-
- 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
- our present invention embraces ore flotation by the use of products of reaction of phosphorus sulfides (such as the trisulfide, P8283, or pentasulfide, 'PazSs), with certain compounds which may be organic or organicinorganic.
- phosphorus sulfides such as the trisulfide, P8283, or pentasulfide, 'PazSs
- the phosphosulfo compounds above referred to can be used either alone or mixed with other oily materials having flotation value, or with solvent agents or mixtures of the same.
- mercaptans may be reacted with phosphorus pentasulflde in a similar manner, for example about three parts of n-amyl mercaptan and one part of phosphorus pentasulfide at 115 C., or thereabout, readily combine to form a syrupy liquid product, hydrogen sulfide being a by-prodnot of the reaction.
- the alkali mercaptans like the alkali alcoholates, combine with phosphorus pentasulflde.
- Phosphorus trisulflde may be used instead of the pentasulflde in the examples given, this being employed in an equimolecular proportion under very much the same-reaction conditions.
- reaction products in the above examples are sufliciently soluble in water so that in the flotation operation they are quickly dispersed as an aqueous solution throughout. the pulp.
- alcohol such as ethyl alcohol. It is to be understood that other alcohols or mixtures thereof, such as denaturedalcohol, methyl, propyl alcohol and higher alcohols can be likewise employed.
- alcoholates may use the alcoholates produced from methyl alcohol, ethyl alcohol, propyl alcohol or some higher alcohols, or mixtures thereof, such as denatured alcohols. The alcoholates containing more than five carbon atoms are not as suitable.
- alkali metal salts as constituting the flotation agent or substance used in the preparation thereof. We desire it understood that while we have secured satisfactory results with the far as these are soluble in oil or water or emulsions thereof. The procedure for making the alkaline earth metal salts, etc., will be obvious from the above disclosure.
- the compounds formed according to the above specification may be described as the alkali and alkaline earth metal salts of the organic thiophosphoric acid compounds of the substances herein classified, to wit:alcohols, phenols and mercaptolic substances.
- a process which comprises reacting on a mercaptolic substance with a phosphorus sulflde to form a reagent having collecting power in ore flotation.
- a process which comprises the froth flotation of metalliferous material in the presence of a reaction product of a mercaptol with a phosphorus sulfide and a frothing agent.
- the step of floating material to be concentrated in the presence of the herein described flotation agent which comprises a reaction product of a phosphorussulfur compound with a substance selected from the herein described group consisting of (a) alkali and alkaline earth phenolates, (b) alkali and alkaline earth alcoholates, in the presence of a solvent, and (c) mercaptolic substances.
- phosphorus-sulfur compound on'orzenicinorganic substance selected-from the'herein de- I scribed group consisting of alkali andaiknline.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Reissued June 5, 1934 PROCESS OF I'LOTA'I'ION Ira 1!. Derby and Orin D. Cunningham,
assignorstoPeterQBelllyJndiam- I apolis, Ind.
No Drawing Indian- Original No. 1,812,839, dated June 30, 1981, Serial No. 96,061, March 19, 1926. Application for reissue March 9, 1984, Serial No.
7 Claims. (CL 209-166) sulfur, that is, compounds structurally consisting of atoms and groups of atoms (or radicals) united to one or more phosphorus atoms as a nucleus, which compounds also contain sulfur. The invention is based upon our observation that certain compounds as described herein, which structurally consist of phosphorus as a nucleus to which the other atoms or groupsof atoms (radicals) are attached, and which contain sulfur, are excellent flotation agents and constitute a class of compounds that have not heretofore been used in the art of flotation. The present invention is characterized especially by the use oi such substances (whether or not they are known per se) as flotation or collecting agents in froth flotation.
More particularly, our present invention embraces ore flotation by the use of products of reaction of phosphorus sulfides (such as the trisulfide, P8283, or pentasulfide, 'PazSs), with certain compounds which may be organic or organicinorganic.
We give the following classification of some of the reactions that yield nuclear phosphorus compoun which can conveniently be employed in ore flotation in accordance with the present invention, namely, the reaction of a phosphorus sulflde such as phosphorus pentasulphide, P285, with (a) the alkali metal salts or alkaline earth salts of coal tar phenols, such as potassium phenolate or sodium cresylate or the like; (b) the alkali or alkaline earth metal salts of alcohols and particularly those mono-hydroxy alcohols containing not more than five carbon atoms, such as sodium ethylate; (c) certain aliphatic mercaptols, for example, ethyl mercaptol, or the alkali metal salts of certain mercaptols, such as the sodium or potassium salts of ethyl mercaptol; and (d) the salts,
- substance with two or more phosphorus atoms as a nucleus of the molecular structure, or there may be a splitting of the molecule of the phosphorus 'sulflde compound to yield two or more products phorus sulfide by the substitution of some other atoms or groups of atoms (radicals), the resulting product or products being characterized, however, by the presence of a nuclear phosphorus atom or atoms in the molecular structure and the presence of sulfur.
These substances have a very high selective action or collecting power for metalliferous materials, such as sulfide minerals, in mineral flotation operations but are lacking in frothing properties so that any appropriate frothing agent (such for example as pine oil or tar acids), should be employed in conjunction therewith in carrying out the flotation operation. It is not necessary that chemically pure substances be used since the unrefined products can be employed with metallurgical results equally good to those obtained with pure substances.
The phosphosulfo compounds above referred to can be used either alone or mixed with other oily materials having flotation value, or with solvent agents or mixtures of the same.
Generally stated it is suflicient to select the desired organic compound of the above classification, and to react thereupon with. phosphorus pentasulfide or other sulfide of phosphorus, or even with a mixture of phosphorus and sulfur, the reaction being performed in a. suitable container, and at a temperature sufficiently high to cause reaction to take place. In many cases it has been found advisable to employ a mixture of said organic compounds, some of which apparently function as solvents, and may also function as both solvents and reacting materials, including alcohols and tar acids.
For the preparation of the phosphosulfo compounds referred to we give the following specific examplesz- (1) The reaction of sodium alcoholate, for example, with phosphorus pentasulfide, Pass, is preferably carried out in some organic solvent such as alcohol which later may be recovered by distillation. A suitable amount, say one part, of anhydrous sodium allcoholate is dissolved in about 5 parts of anhydrous ethyl alcohol to which is then slowly added with stirring 3.5 parts of P285, the temperature of the reaction mixture being maintained at 50 C., or thereabout until all of the P285 has entered into reaction. The reaction product at room temperature is a clear syrupy liquid. Compounds of the type sodium phenolate also react with phosphorus pentasulflde similarly to sodium alcoholate.
(2) One part of powdered phosphorus pentasulflde and about three parts of benzyl mercaptan thereabout, with constant stirring, until the reaction is complete as evidenced by the disappearance of the solid phosphorus pentasulfide, or by the evolution of an amount of hydrogen sulfide equivalent to one molecule per molecule of phosphorus pentasulflde used. The reaction product is a clear syrupy liquid.
Other mercaptans may be reacted with phosphorus pentasulflde in a similar manner, for example about three parts of n-amyl mercaptan and one part of phosphorus pentasulfide at 115 C., or thereabout, readily combine to form a syrupy liquid product, hydrogen sulfide being a by-prodnot of the reaction.
The alkali mercaptans, like the alkali alcoholates, combine with phosphorus pentasulflde.
It is known that mercaptans of themselves are flotation reagents, but by their chemical combination with phosphorus pentasulfide their flotation activity is increased.
In most of the examples given herein, pure chemicals were used, but crude chemicals may be used with equally good results, except that it is preferable to use anhydrous materials for the reactions of phosphorus pentasulflde with organi substances.
In the examples herein given, we do not limit our claims to the quantities of reacting substances herein named.
The general procedure indicated in the above examples may be applied in chemically combining phosphorus pentasulflde with any of the compounds included in the classification outlined in the early part of this specification. In some instances heat may have to be applied to bring about the desired chemical combination, and in other cases the reaction mixture may desirably be cooled to carry on the reaction in the cold.
Phosphorus trisulflde may be used instead of the pentasulflde in the examples given, this being employed in an equimolecular proportion under very much the same-reaction conditions.
It is preferable not to separate the reaction products in the above examples from the solvents but to use the products in their initial or unrefined condition. In most cases they are sufliciently soluble in water so that in the flotation operation they are quickly dispersed as an aqueous solution throughout. the pulp.
The products obtained by the reaction of certain organic and organic-inorganic substances with phosphorus pentasulfide, as illustrated in the above examples, were employed in the flotation of a copper sulfide ore slime of the Utah Copper Company containing some copper oxides and analyzing about 0.9% copper, in the ratio of one tenth pound of product per ton of dry ore,
. with tar acids as a frothing agent and a lime circuit being employed in conjunction therewith. The ore was subjected to the ordinary flotation operation in the mechanical agitation type of flotation machine and a tailing analyzing 0.06% copper was obtained, together with a high grade concentrate analyzing about 20% copper, corresponding to a recovery of about of the copper value in the ore under treatment.
In other examples we have used both smaller and larger amounts of phosphosulfo compounds, in the flotation of ores, with satisfactory results, and we have also used phosphosulfo compounds both alone and with other flotation agents, with very satisfactory results. Furthermore, we do not limit our conditions for carrying out a flotation operation to those included in the above are mixed together and heated at 115-125 C., or
examples, but may use any type of flotation machine, as for example, the Callow cell, or. instead of an alkaline circuit, we may use a normal or acidcircuit. y
In the above specificationwe have referred to the use of alcohol, such as ethyl alcohol. It is to be understood that other alcohols or mixtures thereof, such as denaturedalcohol, methyl, propyl alcohol and higher alcohols can be likewise employed. We have also referred to alcoholates and may use the alcoholates produced from methyl alcohol, ethyl alcohol, propyl alcohol or some higher alcohols, or mixtures thereof, such as denatured alcohols. The alcoholates containing more than five carbon atoms are not as suitable.
In several of the above examples we have referred to alkali metal salts, as constituting the flotation agent or substance used in the preparation thereof. We desire it understood that while we have secured satisfactory results with the far as these are soluble in oil or water or emulsions thereof. The procedure for making the alkaline earth metal salts, etc., will be obvious from the above disclosure.
, The compounds formed according to the above specification ,involving, for example, the use of sodium alcoholate and sodium phenolate, etc., may be described as the alkali and alkaline earth metal salts of the organic thiophosphoric acid compounds of the substances herein classified, to wit:alcohols, phenols and mercaptolic substances.
In the present case we have described the use of phenolates, alcoholates, and mercaptolic substances, as substances to react with phosphorus sulphides to form a flotation reagent. We have given several examples of such phenolates, etc., which are operative for the purpose, and we believe that certain closely related phenolates, etc., can be used, though there are others that will not serve. The expressions phenolates", etc., as used in this case are accordingly to be construed as covering the examples given herein and products so closely related thereto as to function in a like manner.
What is claimed is:
1. A process which comprises reacting on a mercaptolic substance witha phosphorus sulflde to form a reagent having collecting power in ore flotation.
2. A process which comprises the froth flotation of metalliferous material in the presence of a reaction product of a mercaptol with a phosphorus sulfide and a frothing agent.
3. In the art of froth flotation, the step of floating material to be concentrated in the presence of the herein described flotation agent which comprises a reaction product of a phosphorussulfur compound with a substance selected from the herein described group consisting of (a) alkali and alkaline earth phenolates, (b) alkali and alkaline earth alcoholates, in the presence of a solvent, and (c) mercaptolic substances.
4. A process which comprises froth-flotation while in the presence of the herein described fiotation reagent which is a reaction product of a phosphorus-sulfur compound and an alkali metal salt of a phenol in the presence of tar acids. 5. A process which comprises froth-flotation while in the presence of the herein described flotation reagent which is a reaction product of a mica I. A process which comprises Roth-flotation while inthepresenceotthehereindeccribed' flotation reazent which is. reaction product .0: o
phosphorus-sulfur compound on'orzenicinorganic substance selected-from the'herein de- I scribed group consisting of alkali andaiknline.
ecrthmetalphenolctesrandjalkcliandalkcline earth metal alcoholotee'in'the'prese'nceoto vORIIND. CUNNINGHAM.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE19192E true USRE19192E (en) | 1934-06-05 |
Family
ID=2083118
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US19192D Expired USRE19192E (en) | Process of flotation |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE19192E (en) |
-
0
- US US19192D patent/USRE19192E/en not_active Expired
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