IP Library Granted Patent US 8,701,892
Granted Patent B2
US 8,701,892 · App. 13/976,697 · Granted Apr 22, 2014

Amine-containing formulations for reverse froth flotation of silicates from iron ore

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Quick Facts
Patent No.
US 8,701,892
App. No.
13/976,697
Granted
Apr 22, 2014
Kind
B2
Abstract

The present invention relates to a process for enriching an iron mineral from a silicate-containing iron ore by reverse froth flotation of the ore using a collecting composition comprising: a) a compound of formula R 1 O-A-NH(CH 2 ) n NH 2 (I), wherein R 1 is a straight or branched hydrocarbyl group with 12-15 carbon atoms, A is a group —CH 2 CHXCH 2 —, wherein X is hydrogen or a hydroxyl group, and n is a number 2-6; b) a compound of formula R 2 NH 2 (II), where R 2 is a hydrocarbyl group having 12-14 carbon atoms; c) a compound of formula R 3 NH 2 (III), wherein R 3 is a straight or branched, saturated or unsaturated hydrocarbyl group having 16-22 carbon atoms; and d) optionally a depressing agent for the iron mineral, wherein the amount of a) is at least 65% by weight, based on the total weight of a), b) and c), and at most 90% by weight, based on the total weight of a), b) and c), and wherein the weight ratio between c) and b) is 4:1 to 1:1.

Claims (32)

1. A process for enriching an iron mineral from a silicate-containing iron ore by reverse froth flotation of the ore using a collecting composition comprising the step of contacting the ore with the collecting composition, wherein the collecting composition comprises:

a) a compound of formula R 1 O-A-NH(CH 2 ) n NH 2 (I), wherein R 1 is a straight or branched hydrocarbyl group with 12-15 carbon atoms, A is a group —CH 2 CHXCH 2 —, wherein X is hydrogen or a hydroxyl group, and n is a number 2-6;

b) a compound of formula R 2 NH 2 (II), wherein R 2 is a hydrocarbyl group having 12-14 carbon atoms;

c) a compound of formula R 3 NH 2 (III), wherein R 3 is a straight or branched, saturated or unsaturated hydrocarbyl group having 16-22 carbon atoms; and

d) optionally a depressing agent for the iron mineral,

wherein the amount of a) is at least 65% by weight, based on the total weight of a), b) and c), and at most 90% by weight, based on the total weight of a), b) and c), and wherein the weight ratio between c) and b) is 4:1 to 1:1.

2. A process according to claim 1 wherein the weight ratio between c) and b) is 3:1 to 1:1.

3. A process according to claim 1 comprising a further component d) which is a depressing agent for the iron mineral.

4. A process according to claim 3 wherein the depressing agent is chosen from the group of polysaccharides.

5. A process according to claim 4 wherein component d) is starch.

6. A process according to claim 4 wherein component d) is dextrin.

7. A process according to claim 1 wherein c) is a compound (III) wherein R 3 is a hydrocarbyl group having 16-18 carbon atoms.

8. A process according to claim 1 wherein component b) is added as (coco alkyl)amine.

9. A process according to claim 1 wherein the amine components in the collecting composition are present as ammonium salts in an amount of at least 20% by mole.

10. A process according to claim 1 where the collecting composition comprises a) N-(3-isotridecoxypropyl)-1,3-propane diamine, b) a (coco alkyl)monoamine comprising compounds of formula II, wherein R 2 is a hydrocarbyl group with 12-14 carbon atoms, and c) oleylamine.

11. A process according to claim 1 where the amount of a) is at least 70 and at most 80% by weight, based on the total weight of a), b) and c).

12. A collecting composition comprising

a) a compound having the formula R 1 O-A-NH(CH 2 ) n NH 2 (I), wherein R 1 is a straight or branched hydrocarbyl group with 12-15 carbon atoms, A is a group —CH 2 CHXCH 2 —, wherein X is hydrogen or a hydroxyl group, and n is a number 2-6;

b) a compound having the formula R 2 NH 2 (II), wherein R 2 is a hydrocarbyl group having 12-14 carbon atoms;

c) a compound having the formula R 3 NH 2 (III), wherein R 3 is a straight or branched, saturated or unsaturated hydrocarbyl group having 16-22 carbon atoms; and

d) optionally a depressing agent for the iron mineral,

wherein the amount of a) is at least 65% by weight, based on the total weight of a), b) and c), and at most 90% by weight, based on the total weight of a), b) and c), and wherein the weight ratio between c) and b) is 4:1 to 1:1.

13. A collecting composition according to claim 12 wherein the weight ratio between c) and b) is 3:1 to 1:1.

14. A collecting composition according to claim 12 comprising a further component d) which is a depressing agent for the iron mineral.

15. A collecting composition according to claim 14 wherein the depressing agent is chosen from the group of polysaccharides.

16. A collecting composition according to claim 15 wherein component d) is starch.

17. A collecting composition according to claim 15 wherein component d) is dextrin.

18. A collecting composition according to claim 12 wherein c) is a compound (III) wherein R 3 is a hydrocarbyl group having 16-18 carbon atoms.

19. A collecting composition according to claim 12 wherein component b) is added as (coco alkyl)amine.

20. A collecting composition according to claim 12 wherein the amine components in the collecting composition are present as ammonium salts in an amount of at least 20% by mole.

21. A collecting composition according to claim 12 where the collecting composition comprises a) N-(3-isotridecoxypropyl)-1,3-propane diamine, b) a (coco alkyl)monoamine comprising compounds of formula II, wherein R 2 is a hydrocarbyl group with 12-14 carbon atoms, and c) oleylamine.

22. A collecting composition according to claim 12 where the amount of a) is at least 70 and at most 80% by weight, based on the total weight of a), b) and c).

Assignments (4)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
CHANGE OF ADDRESS Recorded May 15, 2017
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 042745/0406 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2013
From: GUSTAFSSON, JAN OLOF; JUBERG, MALIN
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 030701/0561 →