US2180926A - Substituted biguanides as flotation reagents - Google Patents
Substituted biguanides as flotation reagents Download PDFInfo
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- US2180926A US2180926A US241394A US24139438A US2180926A US 2180926 A US2180926 A US 2180926A US 241394 A US241394 A US 241394A US 24139438 A US24139438 A US 24139438A US 2180926 A US2180926 A US 2180926A
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- United States
- Prior art keywords
- copper
- flotation
- biguanide
- biguanides
- substituted
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- 229940123208 Biguanide Drugs 0.000 title description 32
- 238000005188 flotation Methods 0.000 title description 19
- 150000004283 biguanides Chemical class 0.000 title description 18
- 239000003153 chemical reaction reagent Substances 0.000 title description 14
- 239000010949 copper Substances 0.000 description 24
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 22
- 229910052802 copper Inorganic materials 0.000 description 22
- -1 alkyl radical Chemical class 0.000 description 19
- 238000000034 method Methods 0.000 description 10
- 150000001299 aldehydes Chemical class 0.000 description 8
- 238000009291 froth flotation Methods 0.000 description 8
- 239000007859 condensation product Substances 0.000 description 7
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 7
- 229910052737 gold Inorganic materials 0.000 description 7
- 239000010931 gold Substances 0.000 description 7
- 238000011084 recovery Methods 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000005840 aryl radicals Chemical class 0.000 description 5
- 229910001779 copper mineral Inorganic materials 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 5
- 239000004332 silver Substances 0.000 description 5
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 4
- 238000003556 assay Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- SXFUPIWGUVVUOC-UHFFFAOYSA-N butan-2-yloxy-butan-2-ylsulfanyl-hydroxy-sulfanylidene-lambda5-phosphane Chemical class CCC(C)OP(O)(=S)SC(C)CC SXFUPIWGUVVUOC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- QRJOYPHTNNOAOJ-UHFFFAOYSA-N copper gold Chemical compound [Cu].[Au] QRJOYPHTNNOAOJ-UHFFFAOYSA-N 0.000 description 2
- 239000012458 free base Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- UUBZPMKBMHXGNE-UHFFFAOYSA-N 1-(diaminomethylidene)-2-naphthalen-1-ylguanidine Chemical compound C1=CC=C2C(N=C(N)N=C(N)N)=CC=CC2=C1 UUBZPMKBMHXGNE-UHFFFAOYSA-N 0.000 description 1
- CMEIYVWWZREFEM-UHFFFAOYSA-N 2-ethyl-1-(n'-ethylcarbamimidoyl)guanidine Chemical compound CCN=C(N)NC(N)=NCC CMEIYVWWZREFEM-UHFFFAOYSA-N 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- 101150073597 DLST gene Proteins 0.000 description 1
- 101100295675 Dictyostelium discoideum odhB gene Proteins 0.000 description 1
- 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 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QNMWTTFPYZEDCD-UHFFFAOYSA-N butylsulfanyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical group CCCCSP(O)(O)=S QNMWTTFPYZEDCD-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910052947 chalcocite Inorganic materials 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 1
- 229910052949 galena Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- CUQCMXFWIMOWRP-UHFFFAOYSA-N phenyl biguanide Chemical compound NC(N)=NC(N)=NC1=CC=CC=C1 CUQCMXFWIMOWRP-UHFFFAOYSA-N 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- RZFBEFUNINJXRQ-UHFFFAOYSA-M sodium ethyl xanthate Chemical compound [Na+].CCOC([S-])=S RZFBEFUNINJXRQ-UHFFFAOYSA-M 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 229910001656 zinc mineral Inorganic materials 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
- B03D1/01—Organic compounds containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
- B03D2203/025—Precious metal ores
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S209/00—Classifying, separating, and assorting solids
- Y10S209/901—Froth flotation; copper
Definitions
- This invention relates to the froth flotation of metallic minerals, and particularly to the froth flotation of minerals containing copper.
- R and R1 are either hydrogen, an alkyl radical or an aryl radical.
- flotation of copper present in a 20 mixed ore containing, for example, lead and zinc minerals has been effected by floating ofl the copper and lead in the presence of a depressant for zinc, such as sodium cyanide, and then separating copper from lead.
- a depressant for zinc such as sodium cyanide
- This procedure is often 25 unsatisfactory because it is diflicult to get sufficient depression of the undesired constituents of an ore without affecting the copper recovery.
- the use of the biguanides of the present invention produces excellent recoveries of high grade copper minerals without any appreciable flotation of the undesired constituents although no depressants are added.
- Example 1 Five -20 mesh samples, weighing 600 grams each, of a copper ore containing chalcocite, born- 11.04% sulfur and 73.72% insoluble, were -ground Test: it in a steel rod mill so that substantially all of the "In ore would pass through a 65 mesh sieve, the re- Metallurgical r a H d; Concentrate Telling, assays m um Weight Gold co ert A l u. P610611 05. on Y m Rec. Assay Rec. 02- 0!
- P6130611 Grams Element ozJton percent percent percent percent MSG-mixture of sodium diethyl and di secondary butyl dithiophosphates.- 2.48 2.20 121.5 20.03 ass 80.72 11.81 95.48 0.53 0.14
- the reagents oi the present invention do not, in general, promote the flotation of metallic minerals other than copper minerals, or those activated with copper.
- Example 3 The results of comparative flotation tests are given in the following Table II, the biguanide reagents being added in the grinding circuit and the fifty-fifty mixture of sodium diethyl and disecondary butyl dithiophosphates in the flotation machine. Other conditions are constant in the three tests.
- the value of the presentinvention does not lie inthe recovery of a copper; on the contrary, in many low grade goldcopper ores, the copper is more an undesired impurity than a real metallic value.
- the economics of treating many such ores depend on the amount of cyanide which must be used as in such cases, cyanide constitutes one of the major costs.
- the present invention removes a large portion of the undesired copper impurity without serious gold losses and permits the economic treatment by a combined flotation and cyanidation process of low grade ores which otherwise could not be profitably mined and refined.
- a method of froth'flotation which comprises subjecting an aqueous pulp of a meta1lii.'- 'erous mineral to froth flotation in the presence of a reagent included in the group consisting of substituted biguanides having the following for-, mula:
- R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicals, their acid salts, and their aldehyde condensation products.
- a method of froth flotation which comprises subjecting an aqueous pulp of an ore containing copper to froth flotation in the presence of a reagent included in the group consisting of sub stituted biguanides having the following formula:
- R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicais, their acid salts, and their aldehyde condensation products, removing therefrom the concentrate rich in copper and rejecting the tailing poor in copper.
- a method of differential froth notation which comprises subjecting an aqueouspulp of an ore containing copper and other metallic minerals to froth flotation in the presence of a reagent included in the group consisting of substituted biguanides having the following formula:
- R and R1 are members of the group including hydrogen, alkyl radicals and aryl radi cals. their acid. salts, and their aldehyde condensation products, removing therefrom the concentrate rich in copper and rejecting the telling poor in copper and rich in zinc and lead.
- R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicals.
- R and R1 are members of the group including hydrogen, aliwi radicals and aryl radicals.
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Nov. 21, 1939 PATENT orrics SUBSTITUTED BIGUANIDES AS FLOTATION REAGENTS David Walker Jayne, Jr., ld Greenwich, and
Arvid Emil Anderson, New Canaan,
Conn., as-
signors to American Cyanamid Company, New York, N. Y., a corporation of -Maine No Drawing. Application November 19, 1938. Serial No. 241,394
6 Claims. 7 (Cl. 209-466) This invention relates to the froth flotation of metallic minerals, and particularly to the froth flotation of minerals containing copper.
We have found that substituted biguanides,
their salts and their aldehyde condensation prod- .ucts have a specific flotation promoter action, particularlyon copper minerals,.when used in an alkaline circuit. The cheapest types of biguanides are those-having the following form mula: v
35 in which R and R1 are either hydrogen, an alkyl radical or an aryl radical. These materials are very effective and constitute the preferred embodiment of the invention.
In the past, flotation of copper present in a 20 mixed ore containing, for example, lead and zinc minerals, has been effected by floating ofl the copper and lead in the presence of a depressant for zinc, such as sodium cyanide, and then separating copper from lead. This procedure is often 25 unsatisfactory because it is diflicult to get sufficient depression of the undesired constituents of an ore without affecting the copper recovery. The use of the biguanides of the present invention, however, produces excellent recoveries of high grade copper minerals without any appreciable flotation of the undesired constituents although no depressants are added.
No selective flotation of copper minerals occurs. when the standard potassium or sodium 36 ethyl xanthate reagents are used as promoters,
and it is believed that the surprising result obtained with the compounds of the present invention is due to the formation of water-insoluble copper salts which are readily. floatable. This 40 has not been definitely determined, however, and it should be understood that the invention is in :0 sense limited to any particular theory of ac- The mono-aryl substituted biguanides such as 5 phenyl biguanide, tolyl biguanide, xylyl biguanide, cynnvl biguanide, naphthyl biguanide, and the like, or the aldehyde condensation products thereof such as ethylidene o-tolyl'biguanide, furfurylidene (mixed) xylyl biguanide, and the like, are the preferred modifications of the present invention, but other compounds such as ethyl, isopropyl, butyl, etc., biguanides, diphe'nyl bi guanide, phenyl tolyl biguanide, diethyl biguanide, diisopropyl biguanide, phenyl ethyl biguan- 55 ide, phenyl isopropyl biguanide, and the like, and
their condensation products with acetaldehyde, furfuraldehyde, benzaldehyde, etc., mayalso be used and are included within the scope of the invention. I
We have found a progressive'increase in copper recovery as alkyl loading on the phenyl group is increased up to at. least four carbonatoms in the side chains, i. e., cymyl biguanide, but the higher cost of the cymyl derivatives renders their use uneconomic and the cheaper phenyl and tolyl 1o derivatives are preferred. The simple aldehyde derivatives of the preferred mono-aryl substituted biguanides are more effective than the biguanides from which they are derived, the ethylidene derivatives in turn being more efilcient than the methylene. derivatives, and they are cheap enough to be practicable. The invention is, however, not limited'to these preferred embodiments.
Good copper recoveries are obtained if the reagents of the present invention are used in a circuit having a pH of about 9.5, but the best results are obtained at a pH of about 11-12.
- It is an important advantage of the present invention that it can be applied to a flotation process without necessitating any changes in the fiow sheet of the mill. Thus, for example, it makes no difference whether the reagent is added in the grinding circuit or in the flotation machine and the advantages of the present invention may be enjoyed by merely substituting the biguanides for whatever flotation agent was formerly used. It is alsopossible to use ordinary frothing agents since the products of the present invention do not in any way affect their action.
While we have been referring to the use of the free substituted biguanide bases for the flotation of copper minerals, acid salts of these bases, such as the monohydrochloride, can also be used and are included in the present invention. Whether the substituted biguanide is employed in the form of the free base or acid salt makes no difference since the circuit-is sufliciently alkaline to con-'- vert the' salt to the free base immediately upon addition thereto.
The invention will be described in greater de tail in conjunction with the following specific examples which illustrate the application of the invention to certain typical ores.
Example 1 .Five -20 mesh samples, weighing 600 grams each, of a copper ore containing chalcocite, born- 11.04% sulfur and 73.72% insoluble, were -ground Test: it in a steel rod mill so that substantially all of the "In ore would pass through a 65 mesh sieve, the re- Metallurgical r a H d; Concentrate Telling, assays m um Weight Gold co ert A l u. P610611 05. on Y m Rec. Assay Rec. 02- 0!! P6130611 Grams Element ozJton percent percent percent MSG-mixture of sodium diethyl and di secondary butyl dithiophosphates.- 2.48 2.20 121.5 20.03 ass 80.72 11.81 95.48 0.53 0.14 Ethylidene o-tolyl bi mime 2. 51 a 25 65.1 10. 7a a s4 42. 3e 18. 4s 19. as 1. 45 0. 5s Ethylidene mixed xy yl biguanide 2.1% 2. at 147.8 24. 50 5.97 61.95 9.88 95. 25 1.19 0.16
suiting pulp containing 76.31% of 200 mesh product. The pulp was then transferred to a Fagergren flotation machine; a promoter and frother were added, and the material was floated. The results of comparative flotation tests, wherein the only variable was the type of promoter added, are given in the following Table I.
TABLI I Metallurgical results Heads Concentrate Telling Promot/arused Cu, Assay Assay Dlst. per; Cu, l On, On, cen perperpercent wnt cent cent Sodium ethyl xanthate. 2.68 33.00 86.81 0.33 13.19 Mixed xylyl biguanide hydrochloride 2.68 24.80 82.33 0.52 17. 67 I 2-cymyl biguanide hydroc oride.. 2.64 23.00 92.20 0.23 7.80 Ethylidene o-tolyl bignanide hydrochloride.-. 2.68 28.16 87.32 0. 37 12.68 Ethirlidene (mixed) x yyl biguenide hyorochloride 2.72 25.30 96.04 0.12 3.96
Egamplez Comparative flotation tests. similar to those of Example l'were made on a sulfidelead are containing galena and assaying 8.54% lead, 3.10% iron, 1.86% sulfur and 10.22% insoluble. When 0.02 lb./ton oi the standard potassium ethyl zanthate was used as the promoter, an 80% lead recovery was obtained in a concentrate which assayed 73% lead while 0.068 lb./ton oi ethylidene o-tolyl biguanide hydrochloride as the promoter gave 16% lead recovery in a concentrate which assayed 43.3% lead.
Thus, it can be seen that the reagents oi the present invention do not, in general, promote the flotation of metallic minerals other than copper minerals, or those activated with copper.
Example 3 The results of comparative flotation tests are given in the following Table II, the biguanide reagents being added in the grinding circuit and the fifty-fifty mixture of sodium diethyl and disecondary butyl dithiophosphates in the flotation machine. Other conditions are constant in the three tests. a
The above results show that the ethylidene mixed xylyl biguanide and ethyiidene o-tolyl blguanide give more selective flotation of copper in a gold-copper ore than the dithiophosphate reagent. The fifty-flfty mixture of sodium diethyl and disecondary butyl dithiophosphates, however, is a more powerful promoter for gold than either of the reagents covered by the present invention. This permits a more-efiective separation of copper from gold. Since copper compounds are well known cyanicides, the present invention permits important savings in cyanide where gold-copper ores are treated by a combined flotation and cyanide process. In such cases, the value of the presentinvention does not lie inthe recovery of a copper; on the contrary, in many low grade goldcopper ores, the copper is more an undesired impurity than a real metallic value. The economics of treating many such ores depend on the amount of cyanide which must be used as in such cases, cyanide constitutes one of the major costs. The present invention removes a large portion of the undesired copper impurity without serious gold losses and permits the economic treatment by a combined flotation and cyanidation process of low grade ores which otherwise could not be profitably mined and refined.
When copper-containing precious metal ores which are relatively rich in silver are treated by the process described in Example 3, similar results are obtained, the substituted biguanides showing the same selective action in the case of ores containing silver as they do with ores containing gold. 'The economic importance in the case of silver ores is not usually as great as with low grade gold ores, but the savings are nevertheless material and the present invention can be .eiiectivcly used in treating copper-containing silver ores. or silver and gold ores.
What we claim is:
1. A method of froth'flotation which comprises subjecting an aqueous pulp of a meta1lii.'- 'erous mineral to froth flotation in the presence of a reagent included in the group consisting of substituted biguanides having the following for-, mula:
in which R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicals, their acid salts, and their aldehyde condensation products.
'2. A method of froth flotation which comprises subjecting an aqueous pulp of an ore containing copper to froth flotation in the presence of a reagent included in the group consisting of sub stituted biguanides having the following formula:
B NH NE mt-m-t-m in which R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicais, their acid salts, and their aldehyde condensation products, removing therefrom the concentrate rich in copper and rejecting the tailing poor in copper.
3. A method of differential froth notation which comprises subjecting an aqueouspulp of an ore containing copper and other metallic minerals to froth flotation in the presence of a reagent included in the group consisting of substituted biguanides having the following formula:
the group consisting of substituted biguanidee having the following formula:
3 NE NE x- -omi-mn B. in which R and R1 are members of the group including hydrogen, alkyl radicals and aryl radi cals. their acid. salts, and their aldehyde condensation products, removing therefrom the concentrate rich in copper and rejecting the telling poor in copper and rich in zinc and lead.
5. A method of froth flotation according to claim 3 in which the reagent used is an aldehyde condensation product of a substituted biguanide having the following general formula:
" in which R and R1 are members of the group including hydrogen, alkyl radicals and aryl radicals. i
6. A method of froth flotation according to claim 8 in which the reagent'used is an aldehyde condensation product of a substituted biguanide having the following general formula:
1?. r311 NH N-t m t-m R1 in which R and R1 are members of the group including hydrogen, aliwi radicals and aryl radicals.
DAVID W JAYNE. Je. ARVID EMIL ANDERSON v CERTIEICATE 0F CORRECTION. PatentNo. 2,180,926. November 21, 1939. DAVID-MIXER JAYNE, 5PM, ET AL.
It is hereby certified that error appea rsin the printed specification of the above numbered petent requiring correctionas follows: Page 3, secand that the said Letters Patent should read with this cc-rrection therein that the same may conform-to the record of the case in the Patent Office.
igned and sealed this 16th dayof January, A. D. 1910.
1 f i 4 i enry m: Aredale, {Seal} Acting Commissioner of Pa: .fis.
Y and calm, line 11;, claim 5, for the claim reference nmneral 5" read 1';
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US (1) | US2180926A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3805951A (en) * | 1972-04-07 | 1974-04-23 | American Cyanamid Co | Selective flocculation and flotation of slimes from sylvinite ores |
US3819048A (en) * | 1972-09-01 | 1974-06-25 | Continental Oil Co | Oxide copper ore flotation using condensation reaction product as flotation reagent |
US4090867A (en) * | 1975-04-30 | 1978-05-23 | Canadian Patents & Development Limited | Flotation of non-sulphide copper ores |
US20070012630A1 (en) * | 2004-12-23 | 2007-01-18 | Georgia-Pacific Resins, Inc. | Amine-aldehyde resins and uses thereof in separation processes |
US20080017552A1 (en) * | 2004-12-23 | 2008-01-24 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US20080029460A1 (en) * | 2004-12-23 | 2008-02-07 | Georgia-Pacific Chemicals Llc. | Amine-aldehyde resins and uses thereof in separation processes |
US7913852B2 (en) | 2004-12-23 | 2011-03-29 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US8092686B2 (en) | 2004-12-23 | 2012-01-10 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US8702993B2 (en) | 2004-12-23 | 2014-04-22 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
-
1938
- 1938-11-19 US US241394A patent/US2180926A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3805951A (en) * | 1972-04-07 | 1974-04-23 | American Cyanamid Co | Selective flocculation and flotation of slimes from sylvinite ores |
US3819048A (en) * | 1972-09-01 | 1974-06-25 | Continental Oil Co | Oxide copper ore flotation using condensation reaction product as flotation reagent |
US4090867A (en) * | 1975-04-30 | 1978-05-23 | Canadian Patents & Development Limited | Flotation of non-sulphide copper ores |
US20070012630A1 (en) * | 2004-12-23 | 2007-01-18 | Georgia-Pacific Resins, Inc. | Amine-aldehyde resins and uses thereof in separation processes |
US20080017552A1 (en) * | 2004-12-23 | 2008-01-24 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US20080029460A1 (en) * | 2004-12-23 | 2008-02-07 | Georgia-Pacific Chemicals Llc. | Amine-aldehyde resins and uses thereof in separation processes |
US7913852B2 (en) | 2004-12-23 | 2011-03-29 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US8011514B2 (en) * | 2004-12-23 | 2011-09-06 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US8092686B2 (en) | 2004-12-23 | 2012-01-10 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
US8127930B2 (en) * | 2004-12-23 | 2012-03-06 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
US8702993B2 (en) | 2004-12-23 | 2014-04-22 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
US8757389B2 (en) | 2004-12-23 | 2014-06-24 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
US10150839B2 (en) | 2004-12-23 | 2018-12-11 | Ingevity South Carolina, Llc | Amine-aldehyde resins and uses thereof in separation processes |
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