IP Library Granted Patent US 11,608,417
Granted Patent B2
US 11,608,417 · App. 16/623,232 · Granted Mar 21, 2023

Polysaccharide-elastomer masterbatch compositions

Inventors: Natnael Behabtu (Wilmington, DE); Jeffrey S. Downey (Battersea, CA); Christian Peter Lenges (Wilmington, DE); Tizazu H. Mekonnen (Waterloo, CA)
Assignee: NUTRITION & BIOSCIENCES USA 4, INC.
C08J3/22C08B37/0009C08F136/06C08F136/08C08G18/7664C08J3/005C08J3/16C08K3/013C08K3/041C08K3/042C08K3/045C08K3/24C08K3/30C08K3/36C08K5/09C08K5/17C08K5/54C08L23/16C08J2305/00C08J2307/00C08J2309/02C08J2309/06C08K2003/309
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Quick Facts
Patent No.
US 11,608,417
App. No.
16/623,232
Granted
Mar 21, 2023
Kind
B2
Abstract

Disclosed herein are polysaccharide-elastomer masterbatch compositions and processes for preparing the masterbatch compositions. One method comprises a step of a) mixing i) an aqueous polysaccharide dispersion, or ii) a basic aqueous polysaccharide solution, with a rubber latex solution containing a rubber component to form a mixture. The method further comprises the steps of: b) coagulating the mixture obtained in step a) to produce a coagulated mass; and c) drying the coagulated mass obtained in step b). The masterbatch compositions are useful in preparing rubber-containing articles.

Claims (31)

1. A method of producing a composition, the method comprising:

(a) mixing a rubber latex with an aqueous dispersion to form a mixture;

wherein the aqueous dispersion is of

(i) poly alpha-1,3-glucan, wherein the percentage of glycosidic linkages of the poly alpha-1,3-glucan that are alpha-1,3 is greater than or equal to 50%, or

(ii) a poly alpha-1,3-glucan ester compound represented by Structure I:

wherein

(A) n is at least 6,

(B) each R is independently an —H or a first group comprising —CO—C x —COOH, wherein the —C x — portion of said first group comprises a chain of 2 to 18 carbon atoms,

(C) the poly alpha-1,3-glucan ester compound has a degree of substitution with the first group of about 0.001 to about 3.0, and

(D) the percentage of glycosidic linkages of the poly alpha-1,3-glucan ester compound that are alpha-1,3 is greater than or equal to 50%;

wherein the rubber comprises at least one diene-based sulfur-vulcanizable or peroxide-vulcanizable elastomer;

(b) coagulating the mixture to produce a coagulated mass; and

(c) drying the coagulated mass.

2. The method of claim 1 , wherein the drying of the coagulated mass comprises applying mechanical pressure to the coagulated mass.

3. The method of claim 1 , wherein the coagulating of step (b) comprises adding an inorganic salt to the mixture, wherein the inorganic salt comprises LiCl, NaCl, KCl, CaCl 2 , MgCl 2 , Al 2 (SO 4 ) 3 , a zinc salt, sodium sulfate, potassium sulfate, trisodium phosphate, tripotassium phosphate, potassium pyrophosphate, sodium borate, or a combination thereof.

4. The method of claim 1 , wherein the coagulating of step (b) comprises adding an acid to the mixture, wherein the acid comprises acetic acid, sulfuric acid, nitric acid, boric acid, formic acid, an organic acid, or a combination thereof.

5. The method of claim 1 , wherein the

aqueous dispersion is of said poly alpha-1,3-glucan.

6. The method of claim 1 , wherein the poly alpha-1,3-glucan or the poly alpha-1,3-glucan ester compound is in the form of a wet cake or colloidal dispersion.

7. The method of claim 1 , wherein the at least one diene-based sulfur-vulcanizable or peroxide-vulcanizable elastomer has a Tg below −30° C., as determined by dynamic mechanical analysis.

8. The method of claim 1 , wherein the rubber comprises synthetic polyisoprene, styrene butadiene rubber, ethylene propylene diene monomer rubber, hydrogenated nitrile butadiene rubber, polybutadiene, or neoprene.

9. The method of claim 1 , wherein the mixing of step (a) further comprises adding a filler that comprises silica, carbon black, graphene, fullerene, carbon nanotubes, or a mixture thereof.

10. The method of claim 1 , wherein the mixing of step (a) further comprises adding at least one coupling agent that comprises a silane, alkenyl succinic anhydride, alkylketene dimer, polyetheramine, maleic anhydride, methylene diphenyl diisocyanate, or a mixture thereof.

11. The method of claim 1 , wherein the rubber comprises natural rubber.

12. The method of claim 5 , wherein the percentage of glycosidic linkages of the poly alpha-1,3-glucan that are alpha-1,3 is greater than or equal to 90%.

13. The method of claim 5 , wherein the poly alpha-1,3-glucan is in the form of fibrids.

14. The method of claim 1 , wherein the aqueous dispersion is of said poly alpha-1,3-glucan ester compound.

15. The method of claim 14 , wherein the percentage of glycosidic linkages of the poly alpha-1,3-glucan ester compound that are alpha-1,3 is greater than or equal to 90%.

16. The method of claim 14 , wherein the —C x — portion of said first group comprises a chain of 2 to 6 carbon atoms.

17. The method of claim 1 , wherein the mixing of step (a) further comprises mixing a flocculant with the rubber latex and the aqueous dispersion, wherein the flocculant comprises a cationic polymer or anionic polymer.

18. The method of claim 17 , wherein the flocculant comprises carboxymethyl poly alpha-1,3-glucan.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 28, 2020
From: DUPONT INDUSTRIAL BIOSCIENCES USA, LLC
To: NUTRITION & BIOSCIENCES USA 4, INC.
Reel/Frame 055028/0496 →