Compositions and methods for selective separation of minerals from sulfide ores

Patent metadata

Field	Value
Publication number	US-10369577-B2
Application number	US-201715726810-A
Country	US
Kind code	B2
Filing date	Oct 6, 2017
Priority date	Oct 7, 2016
Publication date	Aug 6, 2019
Grant date	Aug 6, 2019

Abstract

Compositions including blends of one or more acrylamide/allyl thiourea polymer as a first depressant, and one or more carboxyalkyl dithiocarbamate compound as a second depressant, and their use as depressants in the beneficiation of sulfide minerals from ores and/or concentrates are disclosed herein, along with methods for selectively separating value sulfide minerals from non-value sulfide minerals in a froth flotation process for the recovery of such value minerals.

First claim

We claim:

1. A composition of matter comprising a blend of a first depressant and a second depressant,
wherein the first depressant is a polymer having a weight average molecular weight from 1,000 g/mol to 1,000,000 g/mol comprising:
i) X units of an acrylamide derivative according to Formula (I):

wherein
each of R, R 1 , and R 2 is independently chosen from H, C 1 -C 4 alkyl, or C 6 -C 12 aryl; and
X is a residual mole percent fraction by weight based on the total mole percent by weight of Y and Z;

ii) Y units of a thiourea derivative according to Formula (II):

wherein
R 3 is chosen from H, a C 1 -C 4 alkyl, or C 6 -C 12 aryl;
each of R 4 and R 5 is independently chosen from H, C 1 -C 4 hydrocarbyl, or a C 6 -C 12 aryl; and
Y is a mole percent fraction from 1% to 50% by weight based on the total weight of X, Y, and Z; and

iii) Z units of a polymerization residue of any monomer copolymerizable with the derivatives according to Formulas (I) and (II), wherein Z is a mole percent fraction from 0% to 50% by weight based on the total weight of X, Y, and Z; and

wherein the second depressant is a dithiocarbamate compound according to Formula (III):

wherein
R 6 is chosen from H, or a moiety having from 1-12 carbon atoms and one or more functional groups selected from OH, SO 3 − M + , COO − M + , and CONR 8 R 9 , wherein each of R 8 and R 9 is independently chosen from H or C 1 -C 4 alkyl;
R 7 is chosen from a moiety having from 1-12 carbon atoms and one or more functional groups selected from OH, SO 3 − M + , COO − M + , and CONR 8 R 9 , wherein each of R 8 and R 9 is independently chosen from H or C 1 -C 4 alkyl;
each instance of M is independently chosen from a cation selected from the group consisting of alkali metal, metal, or R 10 4 N + , wherein each instance of R 10 is independently chosen from H or a C 1 -C 12 alkyl,

wherein the blend is further characterized as being an aqueous solution; and having 4<pH≤14 at a temperature from −5° C. to 85° C.

2. A composition according to claim 1 , wherein the first depressant and the second depressant are present at a weight ratio in a range from 20:80 to 80:20.

3. A composition according to claim 2 , wherein the weight ratio of the first depressant to the second depressant is from 25:75 to 50:50.

4. A composition according to claim 1 , wherein said blend of the first and second depressant is from 10 to 50 parts by weight, per 100 parts by weight of water, and having 4<pH≤14 at a temperature from 20° C. to 50° C.

5. A composition according to claim 1 , wherein each of R, R 1 , R 2 , R 3 , R 4 , and R 5 is H.

6. A composition according to claim 1 , wherein said first depressant has a weight average molecular weight from 10,000 g/mol to 100,000 g/mol.

7. A composition according to claim 1 , wherein X units of Formula (I) to Y units of Formula (II) is present at a weight ratio in a range from 10:90 to 95:5.

8. A composition according to claim 7 , wherein X units of Formula (I) is greater than 50% and no Z units are present.

9. A composition according to claim 1 , wherein R 6 is H, R 7 is CH 2 COO − M + , and each M + in Formula (III) is K.

10. A composition according to claim 1 , wherein the blend of the first and second depressant further comprises, or is used in combination with, a value mineral enhancing amount of a surface modifying agent.

11. A composition according to claim 10 , wherein the surface modifying agent is one or more compound selected from the group consisting of NaSH, NaCN, Nokes reagent, mercapto ethanol, thioglycolic acid or salts thereof (including sodium, potassium, calcium, magnesium, or aluminum salts), sodium ferrocyanides, potassium ferrocyanides, hydroxyethyl trithiocarbonates, carboxyethyl trithiocarbonates, sodium trithiocarbonates, hydrogen peroxide, ozone, air, oxygen, sulfur dioxide, zinc cyanide, calcium cyanide, arsenic Nokes, mercapto propionic acid, mercapto succinic acid, 2-thiouracil, and thioglycerol.

12. A composition according to claim 10 , wherein the surface modifying agent is NaSH, Na2S, sodium salt of thioglycolic acid, or Nokes reagent and is present from 0.5 wt. % to 99.5 wt. %, based on the total weight of the blend.

13. A method for selectively separating value sulfide minerals from non-value sulfide minerals in a froth flotation process for the recovery of said value minerals from an ore or concentrate containing said value and non-value minerals, the method comprising:
adding to one or more stage of the froth flotation process a first depressant and a second depressant in an amount sufficient to increase the value minerals in the froth, thereby selectively separating the value minerals from the non-value minerals,
wherein the first depressant is a polymer having a weight average molecular weight from 1,000 g/mol to 1,000,000 g/mol comprising:
i) X units of an acrylamide derivative according to Formula (I):

wherein
 each of R, R 1 , and R 2 is independently chosen from H, C 1 -C 4 alkyl, or C 6 -C 12 aryl; and
 X is a residual mole percent fraction by weight based on the total mole percent by weight of Y and Z;

ii) Y units of a thiourea derivative according to Formula (II):

wherein
 R 3 is chosen from H, a C 1 -C 4 alkyl, or C 6 -C 12 aryl;
 each of R 4 and R 5 is independently chosen from H, C 1 -C 4 hydrocarbyl, or a C 6 -C 12 aryl; and
 Y is a mole percent fraction from 1% to 50% by weight based on the total weight of X, Y, and Z; and

iii) Z units of a polymerization residue of any monomer copolymerizable with the derivatives according to Formulas (I) and (II), wherein Z is a mole percent fraction from 0% to 50% by weight based on the total weight of X, Y, and Z; and
wherein the second depressant is a dithiocarbamate compound according to Formula (III):

wherein
 R 6 is chosen from H, or a moiety having from 1-12 carbon atoms and one or more functional groups selected from OH, SO 3 − M + , COO − M + , and CONR 8 R 9 , wherein each of R 8 and R 9 is independently chosen from H or C 1 -C 4 alkyl;
 R 7 is chosen from a moiety having from 1-12 carbon atoms and one or more functional groups selected from OH, SO 3 − M + , COO − M + , and CONR 8 R 9 , wherein each of R 8 and R 9 is independently chosen from H or C 1 -C 4 alkyl;
 each instance of M is independently chosen from a cation selected from the group consisting of alkali metal, metal, or R 10 4 N + , wherein each instance of R 10 is independently chosen from H or a C 1 -C 12 alkyl

Assignees

• Cytec Ind Inc

Inventors

• Brasse Mikael
• Arinaitwe Esau
• Nagaraj Devarayasamudram Ramachandran

Classifications

• B03D1/016

  Macromolecular compounds · CPC title

• B03D2201/04

  Frothers · CPC title

• B03D2201/005

  Dispersants · CPC title

• B03D2201/06

  Depressants · CPC title

• C07C333/14

  Dithiocarbamic acids; Derivatives thereof · CPC title