Flotation reagents and flotation processes utilizing same

Patent metadata

Field	Value
Publication number	US-10130956-B2
Application number	US-201414256042-A
Country	US
Kind code	B2
Filing date	Apr 18, 2014
Priority date	Jul 25, 2008
Publication date	Nov 20, 2018
Grant date	Nov 20, 2018

Abstract

Methods of enhancing recovery of value sulfide and/or precious-metal minerals from an ore containing said minerals and a Mg-silicate, slime forming mineral, and/or clay, and which is subjected to a froth flotation process, by adding to one or more stage of the froth flotation process a froth phase modifier having a polymer containing one or more functional groups, and optionally a monovalent ion modifier enhancing agent, thereby enhancing recovery of a value sulfide mineral and/or a precious metal-bearing mineral.

First claim

What is claimed is:

1. A method of enhancing recovery of a value sulfide and/or precious-metal mineral from an ore containing said minerals and a Mg-silicate, slime forming mineral, and/or clay, and which ore is subjected to a froth flotation process performed under alkaline conditions said method comprising:
adding to one or more stage of the froth flotation process performed under alkaline conditions a froth phase modifier comprising a polymer having a carboxyl group or group that becomes a carboxyl group upon hydrolysis, and a monovalent ion modifier enhancing agent, thereby enhancing recovery of a value sulfide mineral and/or a precious metal-bearing mineral.

2. A method according to claim 1 , wherein said polymer additionally comprises one or more functional groups selected from the group consisting of sulfonate groups or acids thereof, phosphate groups or acids thereof, phosphonate groups or acids thereof, hydroxamate groups or acids thereof, silane groups, silanol groups, and phosphinate groups or acids thereof.

3. A method according to claim 1 , wherein said carboxyl groups or groups that become carboxyl groups upon hydrolysis are provided by compounds selected from the group consisting of maleic acid; acrylic acid; methacrylic acid; ethacrylic acid; itaconic acid; crotonic acid; anhydrides thereof; and combinations thereof.

4. A method according to claim 1 , wherein said polymer is selected from the group consisting of poly(styrene-co-maleic anhydride-co-acrylic acid); poly(vinyl acetate-co-maleic anhydride); poly(N-vinylpyrrolidone-co-maleic anhydride); poly(butyl vinyl ether-co-maleic anhydride); poly(styrene-co-maleic anhydride); poly(styrene-co-acrylic acid); and combinations thereof.

5. A method according to claim 2 , wherein said polymer is selected from the group consisting of silane- and tert-octylamine modified poly(N-vinylpyrrolidone-co-maleic anhydride); poly(allyl sulfonate-co-maleic anhydride); poly(styrene-co-maleic anhydride-co-2-acrylamido-2-methyl-1-propanesulfonic acid); hydroxamated poly(acrylamide-co-vinylphosphonic acid); poly(acrylic acid-co-vinylphosphonic acid); poly(2-acrylamido-2-methyl-1-propanesulfonic acid-co-vinylphosphonic acid); poly(styrene-co-maleic anhydride-co-2-acrylamido-2-methyl-1-propanesulfonic acid); poly(acrylic acid-co-vinylphosphonic acid); poly(2-acrylamido-2-methyl-1-propanesulfonic acid-co-vinylphosphonic acid); 3-aminopropyltriethoxysilane modified poly(styrene-co-maleic anhydride); 3-aminopropyltriethoxysilane modified poly(styrene-co-maleic anhydride-co-acrylic acid); hydroxamated poly(acrylamide-co-2-acrylamido-2-methyl-1-propanesulfonic acid); and combinations thereof.

6. A method according to claim 1 , wherein said monovalent ion modifier enhancing agent is selected from the group consisting of NaOH, KOH, NH 4 OH, LiOH, tetramethyl ammonium hydroxide, tetraethylammonium hydroxide, and mixtures thereof.

7. A method according to claim 6 , wherein the monovalent ion modifier is NaOH.

8. A method according to claim 1 , wherein said froth phase modifier is added in an amount from about 10 g to about 5000 g per ton of ore; from about 25 g to about 2500 g per ton of ore; from about 50 g to about 1500 g per ton of ore; or from about 100 g to about 1000 g per ton of ore.

9. A method according to claim 1 , wherein said monovalent ion modifier enhancing agent is added in an amount from about 10 g to about 5000 g per ton of ore.

10. A method according to claim 9 , wherein said monovalent ion modifier enhancing agent is added in an amount from about 50 g to about 2000 g per ton of ore.

11. A method according to claim 10 , wherein said monovalent ion modifier enhancing agent is added in an amount from about 100 g to about 1500 g per ton of ore.

12. A method according to claim 1 further comprising adding a collector to one or more stages of the froth flotation process.

13. A method according to claim 12 , wherein said collector comprises one or more compounds selected from the group consisting of alkoxycarbonyl alkyl dithiocarbamate; mercaptobenzothiazole; dialkyl dithiocarbamate; diaryl or dialkyl dithiophosphate; dialkyl dithiophosphinate; alkoxycarbonyl alkyl thionocarbamate; allyl alkyl thionocarbamate; allyl alkyl xanthate ester; and dialkyl thionocarbamate.

14. A method according to claim 13 , wherein said collector is a formulation comprising alkoxycarbonyl alkyl dithiocarbamate, dialkyl dithiophosphate, and alkoxycarbonyl alkyl thionocarbamate.

15. A method according to claim 13 , wherein said collector is a formulation comprising mercaptobenzothiazole, sodium dialkyl dithiocarbamate, and sodium dialkyl dithiophosphate.

16. A method according to claim 13 , wherein said collector is a formulation comprising alkoxycarbonyl alkyl thionocarbamate, allyl alkyl xanthate ester, dialkyl thionocarbamate, and aromatic hydrocarbon oil.

17. A method according to claim 12 , wherein said collector is added in an amount from about 5 g to about 500 g per ton of ore; from about 10 g to about 200 g per ton of ore; or from about 20 g to about 100 g per ton of ore.

18. A method according to claim 12 , wherein said collector is added simultaneously with said froth phase modifier and/or said monovalent ion modifier enhancing agent.

19. A method according to claim 1 , wherein said froth phase modifier and/or the monovalent ion modifier enhancing agent is added simultaneously with one or more reagents selected from the group consisting of a dispersant, a pH regulator, a depressant, a modifier, a frother, and an activator.

20. A method according to claim 1 , wherein said ore containing Mg-silicate is selected from the group consisting of a Ni ore containing Mg-silicates and a platinum group metal (PGM) ore containing Mg-silicates.

21. A method according to claim 1 , wherein the polymer further comprises one or more hydrophobic groups selected from the group consisting of: aromatic hydrocarbons; C 3 -C 18 hydrocarbons; alkyl esters; aryl esters; alkyl ethers; and aryl ethers.

22. A method according to claim 21 , wherein said alkyl ester is chosen from one or more members selected from the group consisting of: vinyl acetate, vinyl formate, vinyl propionate, vinyl butyrate, and vinyl isobutyrate.

23. A method according to claim 21 , wherein said alkyl ether is chosen from one or more members selected from the group consisting of: butyl vinyl ether, ethyl vinyl ether, and methyl vinyl ether.

24. A method according to claim 21 , wherein the C 3 -C 18 hydrocarbon is selected from the group consisting of N-hexyl acrylamide, N-propyl acrylamide, and N,N-dipropyl acrylamide.

Assignees

• Cytec Tech Corp

Inventors

• Nagaraj Devarayasamudram Ramachandran
• Bhambhani Tarun
• Vasudevan Mukund
• Deo Puspendu
• Chen Haunn-Lin Tony

Classifications

• C22B3/16

  in organic solutions · CPC title

• B03D2203/02

  Ores · CPC title

• B03D2203/025

  Precious metal ores · CPC title

• B03D1/008

  containing oxygen · CPC title

• B03D1/016 Primary

  Macromolecular compounds · CPC title