Polyamidoamine cationic collectors and methods for making and using same

Patent metadata

Field	Value
Publication number	US-2016114337-A1
Application number	US-201514920855-A
Country	US
Kind code	A1
Filing date	Oct 22, 2015
Priority date	Oct 23, 2014
Publication date	Apr 28, 2016
Grant date	—

Abstract

Compositions, aqueous mixtures that include the composition and an ore, and methods for making and using same. The composition can include an organic acid and a polyamidoamine. The polyamidoamine can have the chemical formula (A). In the chemical formula (A), R 1 and R 2 can independently be a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group, R 3 and R 4 can independently be hydrogen or a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group, each m can be an integer of 1 to 5, and n can be an integer of 2 to 8. The aqueous mixture can include an ore, water, and the composition.

First claim

What is claimed is:

1 . A composition, comprising:
an organic acid; and a polyamidoamine having the chemical formula:

wherein:
R 1 and R 2 are independently a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
R 3 and R 4 are independently hydrogen or a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
each m is an integer of 1 to 5, and
n is an integer of 2 to 8.

2 . The composition of claim 1 , wherein:
R 1 and R 2 are independently a C8 to C24 chain having 0 to 5 unsaturated bonds, R 3 and R 4 are hydrogen, each m is an integer of 2, 3, or 4, and n is an integer of 2, 3, 4, or 5.

3 . The composition of claim 1 , wherein:
R 1 and R 2 are independently a C9 to C20 chain having 0 to 3 unsaturated bonds, R 3 and R 4 are hydrogen, each m is an integer of 2 or 3, and n is an integer of 2, 3, or 4.

4 . The composition of claim 3 , wherein R 1 and R 2 are independently C 9 H 19 , C 9 H 17 , C 9 H 15 , C 9 H 13 , C 11 H 23 , C 11 H 21 , C 15 H 33 , C 15 H 31 , C 15 H 29 , C 17 H 35 , C 17 H 33 , C 17 H 31 , C 17 H 29 , C 19 H 37 , C 19 H 35 , C 19 H 33 , C 19 H 31 , or C 19 H 29 , and wherein n is 2.

5 . The composition of claim 1 , wherein R 1 and R 2 are independently derived from lauric acid, stearic acid, isostearic acid, naphthenic acid, oleic acid, linoleic acid, linolenic acid, palmitic acid, or isomers thereof.

6 . The composition of claim 1 , wherein R 3 and R 4 are independently hydrogen, an amino, an amido, or a C10 to C18 chain having 0 to 3 unsaturated bonds.

7 . The composition of claim 1 , wherein the organic acid comprises glacial acetic acid.

8 . The composition of claim 1 , wherein the composition comprises about 10 wt % to about 60 wt % of the organic acid and about 40 wt % to about 90 wt % of the polyamidoamine, based on a combined weight of the polyamidoamine and the organic acid.

9 . The composition of claim 1 , further comprising about 2 wt % to about 50 wt % of water, based on a combined weight of the polyamidoamine, the organic acid, and the water, wherein the organic acid comprises acetic acid.

10 . The composition of claim 1 , wherein the polyamidoamine comprises a product formed by reacting a polyamine and a fatty acid, wherein the polyamine comprises diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, or any mixture thereof, and wherein the fatty acid comprises tall oil fatty acids, lauric acid, stearic acid, isostearic acid, naphthenic acid, oleic acid, linoleic acid, linolenic acid, palmitic acid, isomers thereof, or any mixture thereof.

11 . The composition of claim 10 , wherein the polyamine comprises diethylenetriamine, tetraethylenepentamine, or a mixture thereof, and wherein the fatty acid comprises tall oil fatty acids, lauric acid, stearic acid, isostearic acid, naphthenic acid, isomers thereof, or any mixture thereof.

12 . The composition of claim 1 , wherein the composition has a viscosity of about 30 cP to about 200 cP at a temperature of 25° C.

13 . An aqueous mixture, comprising:
an ore; water; an organic acid; and a polyamidoamine having the chemical formula:

wherein:
R 1 and R 2 are independently a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
R 3 and R 4 are independently hydrogen or a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
each m is an integer of 1 to 5, and
n is an integer of 2 to 8.

14 . The aqueous mixture of claim 13 , wherein:
R 1 and R 2 are independently C 9 H 15 , C 9 H 13 , C 11 H 23 , C 11 H 21 , C 15 H 33 , C 15 H 31 , C 15 H 29 , C 17 H 35 , C 17 H 33 , C 17 H 31 , or C 17 H 29 , R 3 and R 4 are hydrogen, m is an integer of 2, and n is an integer of 2, 3, or 4.

15 . The aqueous mixture of claim 13 , wherein R 1 and R 2 are independently derived from lauric acid, stearic acid, isostearic acid, naphthenic acid, oleic acid, linoleic acid, linolenic acid, palmitic acid, or isomers thereof.

16 . The aqueous mixture of claim 13 , wherein the organic acid comprises acetic acid, wherein the ore is a phosphorous ore, an iron ore, an aluminum ore, a potassium ore, a sodium ore, a calcium ore, potash, feldspar, bauxite, any mixture thereof, and wherein the aqueous mixture comprises about 0.0001 wt % to about 2 wt % of the polyamidoamine and about 0.0001 wt % to about 2 wt % of the organic acid, based on the weight of the ore.

17 . The aqueous mixture of claim 13 , wherein the polyamidoamine comprises a product formed by reacting a polyamine and a fatty acid, wherein the polyamine comprises diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, or any mixture thereof, and wherein the fatty acid comprises tall oil fatty acids, lauric acid, stearic acid, isostearic acid, naphthenic acid, oleic acid, linoleic acid, linolenic acid, palmitic acid, isomers thereof, or any mixture thereof.

18 . A method for purifying an ore, comprising:
combining an ore, water, an organic acid, and a polyamidoamine to produce an aqueous mixture, wherein the ore comprises an impurity, and wherein the polyamidoamine has the chemical formula:

wherein:
R 1 and R 2 are independently a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
R 3 and R 4 are independently hydrogen or a saturated or unsaturated, substituted or unsubstituted, linear or branched, cyclic, heterocyclic, or aromatic hydrocarbyl group,
each m is an integer of 1 to 5, and
n is an integer of 2 to 8; and

collecting a purified ore having a reduced concentration of the impurity relative to the ore from the aqueous mixture.

19 . The method of claim 18 , wherein the organic acid and the polyamidoamine are combined to produce a cationic collector, wherein the cationic collector, the ore, and water are combined to produce the aqueous mixture, and wherein the organic acid is acetic acid.

20 . The method of claim 19 , wherein the cationic collector comprises about 10 wt % to about 60 wt % of the acetic acid and about 40 wt % to about 90 wt % of the polyamidoamine, based on a combined weight of the polyamidoamine and the acetic acid, wherein the ore is a phosphorous ore, an iron ore, an aluminum ore, a potassium ore, a sodium ore, a calcium ore, potash, feldspar, bauxite, or any mixture thereof, wherein the aqueous mixture comprises about 0.0001 wt % to about 2 wt % of the polyamidoamine and about 0.0001 wt % to about 2 wt % of the organic acid, based on the weight of the ore, and wherein:
R 1 and R 2 are each independently a C9 to C20 chain having 0 to 5 unsaturated bonds, R 3 and R 4 are hydrogen, each m is an integer of 2 or 3, and n is an integer of 2, 3, or 4.

Assignees

• Georgia Pacific Chemicals Llc

Inventors

• Snead David R
• Swift Brian L

Classifications

• B03D1/008

  containing oxygen · CPC title

• B03D1/01

  containing nitrogen · CPC title

• B03D2203/06

  Phosphate ores · CPC title

• B03D1/021 Primary

  for treatment of phosphate ores · CPC title