IP Library Granted Patent US 11,607,696
Granted Patent B2
US 11,607,696 · App. 16/468,533 · Granted Mar 21, 2023

Process to treat phosphate ores

Inventors: Natalija Smolko-Schvarzmayr (Hjälteby, SE); Göran Thomas Ljungdahl (Öjersjö, SE); Johan Ekeroth (Kungälv, SE); Åsa Hele'n Jeanette Kleberger Hellström (Ljungskile, SE); Emelie Svensson (Västra Frölunda, SE)
Assignee: NOURYON CHEMICALS INTERNATIONAL B.V.
B03D1/008B01D21/0084B03D1/016C01B25/01B03D2201/02
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Quick Facts
Patent No.
US 11,607,696
App. No.
16/468,533
Granted
Mar 21, 2023
Kind
B2
Abstract

The present invention relates to a process for treating non-sulfidic ores with a collector composition containing a primary and a secondary collector, wherein the primary collector is selected from the group of amphoteric and anionic surface active compounds and the secondary collector is an ethoxylated fatty acid wherein the average degree of ethoxylation is higher than 0 and less than 2, to collector compositions suitable for use in the above process, and to pulp comprising such collector compositions.

Claims (37)

1. A process comprising the step of treating non-sulfidic ores with a collector composition, wherein the collector composition comprises from 3 to 60 wt % of a secondary collector and from 40 to 97 wt % of at least one primary collector, the wt % being based on a total weight of the primary and secondary collectors, wherein the primary collector is selected from the group of amphoteric and anionic surface-active compounds and the secondary collector is an ethoxylated fatty acid having an average degree of ethoxylation of greater than 0 and less than 2.

2. The process of claim 1 , wherein the ethoxylated fatty acid is of the formula

R—C(O)—O-(EO) n   (I),

wherein R is an alkyl or alkenyl group having 7 to 23 carbon atoms; EO is an ethyleneoxy unit; and n is a number greater than 0.5 and less than 2.

3. The process of claim 2 , wherein R is a hydrocarbyl group having 11 to 21 carbon atoms, is linear or branched, has 0 to 4 double bonds and is optionally substituted with up to 3 hydroxyl substituents.

4. The process of claim 3 , wherein the primary collector is an N-acyl derivative of sarcosine, an N-acyl derivative of glycine, or combinations thereof.

5. The process of claim 3 , wherein the primary collector is an anionic surfactant selected from the group of fatty acids, alkyl benzene sulfonates, alkyl phosphates, alkyl sulfates, alkyl sulfosuccinamates, alkyl sulfosuccinates, alkyl lactylates, alkyl hydroxamates, N-acyl neutral amino acids, and mixtures thereof.

6. The process of claim 3 , wherein the primary collector is an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 10 to 18 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO − and SO 3 − ; n is a number from 0 to 1; p is a number from 0 to 5; and q is a number from 1 to 2.

7. The process of claim 2 , wherein the primary collector is an N-acyl derivative of sarcosine, an N-acyl derivative of glycine, or combinations thereof.

8. The process of claim 2 , wherein the primary collector is an anionic surfactant selected from the group of fatty acids, alkyl benzene sulfonates, alkyl phosphates, alkyl sulfates, alkyl sulfosuccinamates, alkyl sulfosuccinates, alkyl lactylates, alkyl hydroxamates, N-acyl neutral amino acids, and mixtures thereof.

9. The process of claim 2 , wherein the primary collector is an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 10 to 18 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO − and SO 3 − ; n is a number from 0 to 1; p is a number from 0 to 5; and q is a number from 1 to 2.

10. The process of claim 2 , wherein the primary collector is an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 7 to 24 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO − and SO 3 − ; n is a number from 0 to 1; p is a number from 0 to 5; and q is a number from 1 to 2.

11. The process of claim 1 , wherein the primary collector is an anionic surfactant selected from the group of fatty acids, alkyl benzene sulfonates, alkyl phosphates, alkyl sulfates, alkyl sulfosuccinamates, alkyl sulfosuccinates, alkyl lactylates, alkyl hydroxamates, N-acyl neutral amino acids and mixtures thereof.

12. The process of claim 1 , wherein the primary collector is an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 7 to 24 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO— and SO 3 − —; n is a number from 0 to 1; p is a number from 0 to about 5; and q is a number from 1 to 2.

13. The process of claim 1 , wherein the collector composition comprises more than one primary collector.

14. The process of claim 1 , wherein the ore is phosphate ore.

15. The process of claim 1 , wherein the process is a direct flotation process.

16. A process comprising the following steps:

a) conditioning a pulped ore comprising a non-sulfidic mineral and optionally flotation bath adjuncts, in an aqueous solution;

b) adding the collector composition of claim 1 to the aqueous solution;

b) optionally adding one or more additional flotation bath adjuncts and/or one or more depressants to the pulped ore, and c) performing a froth flotation process to recover the non-sulfidic mineral.

17. The process of claim 1 , wherein the primary collector is an N-acyl derivative of sarcosine, an N-acyl derivative of glycine, or combinations thereof.

18. The process of claim 1 , wherein the primary collector is an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 10 to 18 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO − and SO 3 − ; n is a number from 0 to 1; p is a number from 0 to 5; and q is a number from 1 to 2.

19. The process of claim 1 , wherein, the collector composition comprises more than one primary collector, one of the one or more primary collectors comprising an amphoteric surfactant of the following formula

wherein R is a hydrocarbon group having from 8 to 18 carbon atoms; A is an oxyalkylene group having from 2 to 4 carbon atoms; R 1 is selected from the group consisting of hydrogen and hydrocarbon groups having from 1 to 4 carbon atoms; Y − is selected from the group consisting of COO − and SO 3 − ; n is a number from 0 to 1; p is a number from 0 to 5; and q is a number from 1 to 2; and

an anionic surfactant selected from the group of fatty acids, alkyl benzene sulfonates, alkyl phosphates, alkyl sulfates, alkyl sulfosuccinamates, alkyl sulfosuccinates, alkyl lactylates, alkyl hydroxamates, N-acyl neutral amino acids, and mixtures thereof;

the ethoxylated fatty acid is of the formula

R—C(O)—O-(EO) n   (I),

wherein R is a hydrocarbyl group having 11 to 21 carbon atoms, is linear or branched, has 0 to 4 double bonds and is optionally substituted with up to 3 hydroxyl substituents; EO is an ethyleneoxy unit; and n is a number greater than 0.5 and less than 2;

the ore is apatite ore; and

the process is a direct flotation process.

20. A pulp comprising crushed and ground non-sulfidic ore, and a collector composition comprising from 3 to 60 wt % of a secondary collector and from 40 to 97 wt % of a primary collector, the wt % being based on a total weight of the primary and secondary collectors, wherein the primary collector is selected from the group of amphoteric and anionic surface-active compounds and the secondary collector is an ethoxylated fatty acid having an average degree of ethoxylation of greater than 0 and less than 2.

Assignments (2)
CHANGE OF NAME Recorded Apr 7, 2020
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 052328/0499 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2019
From: SMOLKO-SCHVARZMAYR, NATALIJA; LJUNGDAHL, GÖRAN THOMAS; EKEROTH, JOHAN; KLEBERGER HELLSTRÖM, ÅSA HELE'N JEANETTE; SVENSSON, EMELIE
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050398/0514 →
Priority Claims (1)
EP 16206716 · Dec 23, 2016 · regional
Continuity (1)
Related Publication 20200222914A1 · Jul 16, 2020