Electrostatic modification reagent and process for enhancing electrostatic separation in the beneficiation of ores

Patent metadata

Field	Value
Publication number	US-10245596-B2
Application number	US-201615200366-A
Country	US
Kind code	B2
Filing date	Jul 1, 2016
Priority date	Oct 31, 2008
Publication date	Apr 2, 2019
Grant date	Apr 2, 2019

Abstract

An electrostatic modification reagent and a process for beneficiating a mineral substrate by electrostatic separation as described herein. The electrostatic modification reagent may be used in an electric separation process for separating components from a mineral ore or sand.

First claim

What is claimed is:

1. An electrostatic modification reagent for beneficiating a mineral substrate by electrostatic separation, wherein the mineral substrate includes a conducting mineral component and/or a non-conducting mineral component, said reagent comprising:
at least one electrostatic modifier comprising an organic compound selected from the group consisting of
quaternary amines; imidazoline compounds; dithiocarbamate compounds; pyridine compounds; pyrrolidine compounds; conducting polymers; polyethyleneimines; compounds of formula (IV):
R—(CONH—O—X) n   (IV)

wherein n of formula (IV) is 1 to 3; wherein R of formula (IV) comprises from 1 to 50 carbons; and wherein each X of formula (IV) is individually selected from the group consisting of H, M, and NR′ 4 , where M is a metal ion and each R′ is individually selected from the group consisting of H, C 1 -C 10 alkyl, C 6 -C 10 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl;

compounds of formula (VI):

wherein R8 of formula (VI) is selected from the group consisting of H, C 1 -C 22 alkyl, C 6 -C 22 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl; and X of formula (VI) is selected from the group consisting of H, M, and NR′ 4 , where M is a metal ion and each R′ is individually selected from the group consisting of H, C 1 -C 10 alkyl, C 6 -C 10 aryl, C 7 -C 10 aralkyl and C 10 -C 18 naphthylalkyl;

and mixtures thereof;
a plurality of particles having an average specific resistivity that is greater than or equal to the specific resistivity of the non-conducting mineral component of the mineral substrate when the non-conducting mineral component is electrostatically modified; and/or
a plurality of particles having an average specific resistivity that is less than or equal to the specific resistivity of the conducting mineral component of the mineral substrate when the conducting mineral component is electrostatically modified,
wherein the electrostatic modifier and plurality of particles are present in a weight ratio of electrostatic modifier to particles of from 100:1 to 1:100.

2. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises a quaternary amine compound according to formula (I):
R(R 1 R 2 R 3 )N + X −   (I)

wherein R of formula (I) comprises from 1 to 50 carbon atoms;
wherein each of R 1 , R 2 and R 3 of formula (I) is individually chosen from a member selected from the group consisting of H, C 1 -C 10 alkyl, C 6 -C 10 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl; and
wherein X of formula (I) is selected from the group consisting of halide, oxide, sulfide, nitride, hydride, peroxide, hydroxide, cyanide, perchlorate, chlorate, chlorite, hypochlorite, nitrate, nitrite, sulfate, sulfite, phosphate, carbonate, acetate, oxalate, tosylate, cyanate, thiocyanate, bicarbonate, permanganate, chromate, and dichromate.

3. The electrostatic modification reagent according to claim 2 , wherein the quaternary amine compound has a number average molecular weight of 700 Da or less.

4. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises an imidazoline compound comprising
a compound of formula (IIa)

or a quaternized salt thereof;
wherein R 4 ′ is selected from the group consisting of C 1 -C 4 alkylamine, C 1 -C 4 alkoxy and C 2 -C 5 alkyl; and wherein R 4 is selected from the group consisting of H, C 1 -C 26 alkyl, C 2 -C 26 alkenyl, C 6 -C 26 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl; or
a compound of formula (IIb):

wherein R 1 of formula (IIb) is selected from the group consisting of H, C 1 -C 26 alkyl, C 2 -C 26 alkenyl, C 6 -C 26 aryl, C 7 -C 10 aralkyl, C 10 -C 18 naphthylalkyl, and oleyl; and wherein R of formula (IIb) is selected from the group consisting of H, C 1 -C 26 alkyl, oleyl, C 2 -C 26 alkenyl, C 6 -C 26 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl; or
mixtures of a compound according to formula (IIa), or a quaternized salt thereof, and a compound according to formula (IIb).

5. The electrostatic modification reagent according to claim 4 , wherein the imidazoline compound is chosen from
a compound according to formula (IIa), wherein R 4 ′ is a C 1 -C 4 alkoxy and R 4 is a C 1 -C 26 alkyl; or
a compound according to formula (IIb), wherein R is oleyl and R 1 is oleyl; or
mixtures thereof.

6. The electrostatic modification reagent according to claim 5 , wherein the compound according to formula (IIa) is:

7. The electrostatic modification reagent according to claim 5 , wherein the compound according to formula (IIb) is:

8. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises a dithiocarbamate compound.

9. The electrostatic modification reagent according to claim 8 , wherein the dithiocarbamate compound is sodiumdiallylamine dithiocarbamate according to formula VII:

10. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises a pyridine compound according to formula (III):

wherein R of formula (III) is selected from the group consisting of H, C 1 -C 22 alkyl, C 6 -C 22 aryl, C 7 -C 10 aralkyl, and C 10 -C 18 naphthylalkyl; and wherein X of formula (III) is selected from the group consisting of halide, oxide, sulfide, nitride, hydride, peroxide, hydroxide, cyanide, perchlorate, chlorate, chlorite, hypochlorite, nitrate, nitrite, sulfate, sulfite, phosphate, carbonate, acetate, oxalate, tosylate, cyanate, thiocyanate, bicarbonate, permanganate, chromate, and dichromate.

11. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises a conducting polymer comprising a polyaniline compound according to formula (V):

wherein each of X, Y, and Z of formula (V) is individually selected from the group consisting of —COOH, —SO 3 H, and —CO(NH—OH);
wherein R7 of formula (V) is selected from the group consisting of H, C 1 -C 22 alkyl, C 6 -C 22 aryl, C 7 -C 10 aralkyl, C 10 -C 18 naphthylalkyl, sulfate, and hydroxyl; and
wherein n of formula (V) is selected so that the polyaniline has a number average molecular weight from 500 to 10,000 Da.

12. The electrostatic modification reagent according to claim 1 , wherein the electrostatic modifier comprises a compound according to formula (IV) and is chosen from a C 1 -C 10 alkyl hydroxamate, or salts thereof.

13. The electrostatic modification reagent according to claim 12 , wherein the alkyl hydroxamate is selected from the group consisting of mono-, di-, or tri-hydroxamic acids, sodium salts thereof, potassium salts thereof, and mixtures thereof.

Assignees

• Cytec Tech Corp

Inventors

• Ravishankar Sathanjheri A
• Kolla Harsha
• Wang Bing

Classifications

• B03C7/003 Primary

  Pretreatment of the solids prior to electrostatic separation · CPC title

• C01G23/0475

  Purification · CPC title

• H01B1/12

  organic substances {(organic macromolecular compounds or compositions C08)} · CPC title

• C01B33/20

  Silicates (persilicates C01B15/14 {; containing aluminium C01B33/26}) · CPC title