Collector composition

Patent metadata

Field	Value
Publication number	US-12478982-B2
Application number	US-202017637999-A
Country	US
Kind code	B2
Filing date	Aug 28, 2020
Priority date	Aug 29, 2019
Publication date	Nov 25, 2025
Grant date	Nov 25, 2025

Abstract

The present invention relates to a collector composition for the beneficiation of lithium silicates and magnesium silicates from an ore comprising different silicate minerals, their use in flotation processes and a method for the beneficiation of lithium silicates- and magnesium silicates-containing minerals using said collector composition.

First claim

The invention claimed is:

1 . A method comprising beneficiating lithium silicate minerals and magnesium silicate minerals from an ore comprising different silicate minerals, utilizing a collector composition, wherein the collector composition comprises:
A. at least one component (A) selected from compounds of formula (I) and salts thereof,
G 1 -C(═O)—NR—CH(R 1 )—C(═O)—OH  formula (I),

wherein G 1 is a linear or branched, substituted or unsubstituted, saturated or unsaturated C 6 -C 30 hydrocarbon chain; and
R and R 1 independent of each other are selected from the group consisting of hydrogen and linear or branched, substituted or unsubstituted, saturated or unsaturated C 1 -C 30 hydrocarbon chain; and
B. at least one component (B) selected from the group consisting of saturated or unsaturated alcohols containing at least 10 carbon atoms (B1) and an ester containing at least 10 carbon atoms (B2) derived from a mono-, di- or tri-functional carboxylic acid.

2 . The method according to claim 1 , wherein the lithium silicate or magnesium silicate minerals are selected from the group consisting of spodumene, petalite, lepidolite, hectorite, olivine and forsterite.

3 . The method according to claim 1 , wherein R 1 is selected from the group consisting of hydrogen, —CH 3 , —CH(CH 3 )CH 2 CH 3 , —CH 2 —CH(CH 3 )CH 3 , —CH(CH 3 ) 2 , —CH 2 CH 2 SCH 3 , —CH 2 -phenyl, —CH 2 (indolyl), —CH 2 -C 4 H 4 —OH, —CH 2 —SH, —CH 2 CH 2 C(═O) NH 2 , —CH 2 (OH) and —CH(OH)CH 3 .

4 . The method according to claim 1 , wherein R is selected from the group consisting of hydrogen, —CH 3 , —C 2 H 5 and —C 3 H 7 .

5 . The method according to claim 1 , wherein G 1 is a linear or branched, unsubstituted, saturated or unsaturated C 8 -C 20 hydrocarbon chain.

6 . The method according to claim 1 , wherein the salts are selected from the group consisting of sodium salts, potassium salts and ammonium salts.

7 . The method according to claim 1 , wherein the compound of formula (I) and salts thereof is selected from the group consisting of N-oleoyl sarcosine, N-lauroyl sarcosine, N-cocoyl sarcosine, N-myristoyl sarcosine, N-palmityl sarcosine, N-stearyl sarcosine, N-vaccenyl sarcosine, N-eicosenoyl sarcosine, N-erucyl sarcosine, N-eicosadienoyl sarcosine, N-docosadienoyl sarcosine, N-linolenyl sarcosine, N-linoleyl sarcosine, sodium N-oleoyl sarcosinate, sodium N-lauroyl sarcosinate, sodium N-cocoyl sarcosinate, sodium N-myristoyl sarcosinate, sodium N-palmityl sarcosinate, sodium N-stearyl sarcosinate, sodium N-vaccenyl sarcosinate, sodium N-eicosenoyl sarcosinate, sodium N-erucyl sarcosinate, sodium N-eicosadienoyl sarcosinate, sodium N-docosadienoyl sarcosinate, sodium N-linolenyl sarcosinate, sodium N-linoleyl sarcosinate, potassium N-oleoyl sarcosinate, potassium N-lauroyl sarcosinate, potassium N-cocoyl sarcosinate, potassium N-myristoyl sarcosinate, potassium N-palmityl sarcosinate, potassium N-stearyl sarcosinate, potassium N-vaccenyl sarcosinate, potassium N-eicosenoyl sarcosinate, potassium N-erucyl sarcosinate, potassium N-eicosadienoyl sarcosinate, potassium N-docosadienoyl sarcosinate, potassium N-linolenyl sarcosinate, potassium N-linoleyl sarcosinate, ammonium N-oleoyl sarcosinate, ammonium N-lauroyl sarcosinate, ammonium N-cocoyl sarcosinate, ammonium N-myristoyl sarcosinate, ammonium N-palmityl sarcosinate, ammonium N-stearyl sarcosinate, ammonium N-vaccenyl sarcosinate, ammonium N-eicosenoyl sarcosinate, ammonium N-erucyl sarcosinate, ammonium N-eicosadienoyl sarcosinate, ammonium N-docosadienoyl sarcosinate, ammonium N-linolenyl sarcosinate and ammonium N-linoleyl sarcosinate.

8 . The method according to claim 1 , wherein the saturated or unsaturated alcohols (B1) contain 10 to 40 carbon atoms.

9 . The method according to claim 1 , wherein the saturated or unsaturated alcohols (B1) have a degree of branching in the range of 1 to 3.

10 . The method according to claim 1 , wherein the saturated or unsaturated alcohol (B1) is a branched, saturated C 10 -C 16 alcohols.

11 . The method according to claim 1 , wherein the esters containing at least 10 carbon atoms (B2) are selected from the group consisting of monoesters containing at least 10 carbon atoms (B2a), diesters containing at least 10 carbon atoms (B2b) and triesters containing at least 10 carbon atoms (B2c).

12 . The method according to claim 11 , wherein the monoesters containing at least 10 carbon atoms (B2a) are selected from the group consisting of caproic acid butyl ester, caproic acid pentyl ester, caproic acid hexyl ester, caproic acid cyclohexyl ester, caproic acid octyl ester, caproic acid isooctyl ester, caproic acid nonyl ester, caproic acid decyl ester, caproic acid lauryl ester, caproic acid myristyl ester, caproic acid cetyl ester, caproic acid pamitoleyl ester, caproic acid heptadecyl ester, caproic acid stearyl ester, caproic acid oleyl ester, caproic acid nonadecyl ester, caproic acid arachidyl ester, caproic acid henicosyl ester, caproic acid behenyl ester, caproic acid erucyl ester, caprylic acid butyl ester, caprylic acid pentyl ester, caprylic acid hexyl ester, caprylic acid cyclohexyl ester, caprylic acid octyl ester, caprylic acid isooctyl ester, caprylic acid nonyl ester, caprylic acid decyl ester, caprylic acid lauryl ester, caprylic acid myristyl ester, caprylic acid cetyl ester, caprylic acid pamitoleyl ester, caprylic acid heptadecyl ester, caprylic acid stearyl ester, caprylic acid oleyl ester, caprylic acid nonadecyl ester, caprylic acid arachidyl ester, caprylic acid henicosyl ester, caprylic acid behenyl ester, caprylic acid erucyl ester, capric acid butyl ester, capric acid pentyl ester, capric acid hexyl ester, capric acid cyclohexyl ester, capric acid octyl ester, capric acid isooctyl ester, capric acid nonyl ester, capric acid decyl ester, capric acid lauryl ester, capric acid myristyl ester, capric acid cetyl ester, capric acid pamitoleyl ester, capric acid heptadecyl ester, capric acid stearyl ester, capric acid oleyl ester, capric acid nonadecyl ester, capric acid arachidyl ester, capric acid henicosyl ester, capric acid behenyl ester, capric acid erucyl ester, lauric acid butyl ester, lauric acid pentyl ester, lauric acid hexyl ester, lauric acid cyclohexyl ester, lauric acid octyl ester, lauric acid isooctyl ester, palmitic acid butyl ester, palmitic acid pentyl ester, palmitic acid hexyl ester, palmitic acid cyclohexyl ester, palmitic acid octyl ester, palmitic acid isooctyl ester, palmitic acid nonyl ester, palmitic acid decyl ester, palmitic acid lauryl ester, palmitic acid myristyl ester, palmitic acid cetyl ester, palmitic acid pamitoleyl ester, palmitic acid heptadecyl ester, palmitic acid stearyl ester, palmitic acid oleyl ester, palmitic acid nonadecyl ester, palmitic acid arachidyl ester, palmitic acid henicosyl ester, palmitic acid behenyl ester, palmitic acid erucyl ester, d nonyl ester, lauric acid decyl ester, lauric acid lauryl ester, lauric acid myristyl ester, lauric acid cetyl ester, lauric acid pamitoleyl ester, lauric acid heptadecyl ester, lauric acid stearyl ester, lauric acid oleyl ester, lauric acid nonadecyl ester, lauric acid arachidyl ester, lauric acid henicosyl ester, lauric acid behenyl ester, lauric acid erucyl ester, myristic acid butyl ester, myristic acid pentyl ester, myristic acid hexyl ester, myristic acid cyclohexyl ester, myristic acid octyl ester, myristic acid isooctyl ester, myristic acid nonyl ester, myristic acid decyl ester, myristic acid lauryl ester, myristic acid myristyl ester, myristic acid cetyl ester, myristic acid pamitoleyl ester, myristic acid heptadecyl ester, myristic acid stearyl ester, myristic acid oleyl ester, myristic acid no

Assignees

• Basf Se

Inventors

• Michailovski Alexej
• Chipfunhu Daniel
• Dickie Scott Alexander

Classifications

• C01B33/325

  After-treatment, e.g. purification or stabilisation of solutions, granulation; Dissolution; Obtaining solid silicate, e.g. from a solution by spray-drying, flashing off water or adding a coagulant · CPC title

• C01B33/22

  Magnesium silicates · CPC title

• B03D2201/02

  Collectors · CPC title

• B03D1/01

  containing nitrogen · CPC title

• B03D1/008 Primary

  containing oxygen · CPC title