Method for preparing functionalized graft polymers

Patent metadata

Field	Value
Publication number	US-9708422-B2
Application number	US-201415034029-A
Country	US
Kind code	B2
Filing date	Nov 25, 2014
Priority date	Dec 10, 2013
Publication date	Jul 18, 2017
Grant date	Jul 18, 2017

Abstract

An acylated hydrocarbon polymer is aminated by reacting a primary or secondary aromatic amine which is solid at room temperature with an acyl group of the polymer, by: supplying a melt of the acylated polymer; supplying a solution of the aromatic amine in a polar aprotic solvent which has a boiling point of at least about 15° C., a melting point below about 40° C., and a dielectric constant of at least about 5° at 25° C.; mixing the solution at 140° C. to 185° C.; and cooling the resulting amine-reacted polymer with a liquid while retaining the polar aprotic solvent in the polymer.

First claim

What is claimed is:

1. A method for aminating an acylated hydrocarbon polymer by reacting a primary or secondary aromatic amine which is solid at room temperature with an acyl group of said polymer, comprising the steps of:
(a) supplying a melt of said acylated hydrocarbon polymer;
(b) supplying a liquid solution of about 20 to about 60 percent by weight of said aromatic amine in a polar aprotic solvent which has a boiling point (at atmospheric pressure) of at least about 150 ° C., a melting point below about 40 ° C., and a dielectric constant of at least about 5 at 25 ° C.;
(c) mixing the solution of said aromatic amine with the melt of said polymer in a mixing device at a temperature of about 140 ° C. to about 185 ° C.; whereby said aromatic amine reacts with acyl group of said polymer; and
(d) cooling the resulting amine-reacted polymer.

2. The method of claim 1 wherein the amine-reacted polymer is cooled by a cooling liquid comprising water or an oil.

3. The method of claim 1 wherein a majority of the polar aprotic solvent is retained in the cooled amine-reacted polymer.

4. The method of claim 1 wherein the cooling of the amine-reacted polymer is effected in an underwater pelletizer.

5. The method of claim 1 wherein the mixing device comprises an extruder, wherein the polymer is melted and the solution of the amine is mixed with the melted polymer in said extruder.

6. The method of claim 1 wherein the acylated hydrocarbon polymer comprises an acylated olefin copolymer.

7. The method of claim 1 wherein the acylated hydrocarbon polymer comprises an acylated hydrocarbon homopolymer.

8. The method of claim 1 wherein the acylated hydrocarbon polymer comprises an acylated copolymer of a vinyl aromatic monomer and one or more conjugated diene monomers.

9. The method of claim 8 wherein the vinyl aromatic monomer is styrene and the conjugated diene monomer is isoprene or butadiene.

10. The method of claim 6 wherein the monomers of the acylated hydrocarbon copolymer comprise ethylene and at least one alpha-olefin of 3 to about 12 carbon atoms and, optionally, a non-conjugated diene.

11. The method of claim 10 wherein the alpha-olefin comprises propylene, 1-butene, or mixtures thereof.

12. The method of claim 1 wherein said acylated hydrocarbon polymer comprises at least one succinic acid or succinic anhydride moiety grafted onto the backbone thereof.

13. The method of claim 1 wherein the amount of the polar aprotic solvent is about 1 to about 40 percent by weight of the amount of the acylated hydrocarbon polymer.

14. The method of claim 1 wherein the solution of the amine is maintained at a temperature of about 15° C. to about 40° C. when it is added to the mixing device.

15. The method of claim 1 wherein the aromatic amine comprises 3 -nitroaniline, 4-(4-nitrophenylazo)aniline (Disperse Orange 3), aminodiphenylamine, the reaction product of isatoic anhydride and aminodiphenylamine, or mixtures thereof.

16. The method of claim 1 wherein the polar aprotic solvent comprises N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethyl acetamide, N,N-diethylacetamide, tetramethylene sulfone, a dialkyl ether of an alkylene glycol or of a di(alkylene glycol), or mixtures thereof.

17. The method of claim 1 further comprising adding an aliphatic amine having a single primary amino group to the mixture of step (c) after addition of said aromatic amine.

18. The method of claim 1 wherein the acyl group on the acylated hydrocarbon polymer is a pendant group derived from an acylating agent comprising maleic anhydride, maleic acid, itaconic anhydride, or itaconic acid, which is grafted onto the backbone of said polymer prior to mixing the melted polymer with the solution of the aromatic amine.

19. The method of claim 1 wherein the acylated hydrocarbon polymer is prepared by grafting the backbone of said polymer with the acylating agent in the presence of a peroxide in a first extruder, and subsequently contacting the melted grafted polymer with the solution of the aromatic amine in the first extruder or in a second extruder.

20. The method of claim 19 wherein at least one of the first or, if present, the second extruder, comprises at least one venting zone suitable for removing volatile materials from the reaction mixture.

Assignees

• Lubrizol Corp

Inventors

• Proust Nicolas
• Covitch Michael J

Classifications

• C10N2030/02

  Pour-point; Viscosity index · CPC title

• C10M2205/04

  containing aromatic monomers, e.g. styrene · CPC title

• C10N2040/252

  Diesel engines · CPC title

• C10M2205/026

  Butene · CPC title

• C10M2217/028

  containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring · CPC title