IP Library › Granted Patent US 11,485,797
Granted Patent B2
US 11,485,797 · App. 16/303,165 · Granted Nov 1, 2022

Production of chemically derivatized nanocellulose

Inventors: Rhodri Williams (Edinburgh, GB); Robert English (Eilean Siar, GB); John Heaton (Maastricht, GB)
Assignee: SAPPI Netherlands Services B.V.
C08B11/12C08B11/14C08B11/15C08B15/08C08J3/05C08J3/12C08J2301/10C08J2301/28
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,485,797
App. No.
16/303,165
Granted
Nov 1, 2022
Kind
B2
Abstract

The present invention provides a method for the production of chemically derivatized nanocellulose, comprising the step of a. contacting a precursor cellulosic material with a chemically derivatizing composition to form a liquid reaction mixture, and b. chemically reacting the formed liquid reaction mixture, and c. subjecting the formed liquid reaction mixture to microfluidisation, wherein the steps b. and c. are carried out simultaneously.

Claims (32)

1. A method for the production of chemically derivatized nanocellulose, comprising the step of:

a. contacting a precursor cellulosic material with a chemically derivatizing composition to form a liquid reaction mixture,

b. chemically reacting the formed liquid reaction mixture, and

c. subjecting the formed liquid reaction mixture to microfluidisation,

wherein the steps b. and c. are carried out simultaneously, and

wherein the chemically derivatizing composition comprises an acylating agent.

2. The method according to claim 1 , wherein the precursor cellulosic material is a suspension of precursor cellulosic material in a liquid phase.

3. The method according to claim 1 , wherein the chemically derivatizing composition is a liquid chemically derivatizing composition.

4. The method according to claim 1 , wherein the chemically derivatizing composition further comprises an acid or a base as a catalyst, and the chemically derivatized nanocellulose is acylated nanocellulose.

5. The method according to claim 4 , wherein the acylating agent is an acylating agent that provides for a C1-C4 acyl moiety and the catalyst is an acid.

6. The method according to claim 4 , wherein the acylating agent is an acylating agent that provides for a C1-C4 acyl moiety, where the acetylating agent is chosen from formic, acetic, butyric and propionic acid.

7. The method according to claim 1 ,

wherein the chemically derivatizing composition consists of an alkenyl carboxylate and a base and the precursor cellulosic material is a suspension of precursor cellulosic material in acetone, and

wherein the acetone is removed from the liquid reaction mixture prior to step b.

8. The method according to claim 7 , wherein the alkenyl carboxylate is a vinyl carboxylate and wherein the base is a non-nucleophilic base.

9. The method according to claim 1 , wherein the precursor cellulosic material is chemically unmodified nanocellulose.

10. The method according to claim 1 , wherein the precursor cellulosic material is chemically unmodified nanocellulose in dry form.

11. The method for the production of chemically derivatized nanocellulose according to claim 1 , comprising the steps of:

a. contacting a precursor cellulosic material which is a chemically unmodified nanocellulose with a chemically derivatizing composition to form a liquid reaction mixture,

b. chemically reacting the formed liquid reaction mixture, and

c. subjecting the formed liquid reaction mixture to microfluidisation,

wherein the steps b. and c. are carried out simultaneously, and

wherein the chemically derivatizing composition is a liquid chemically derivatizing composition comprising a acylating agent suspended or dissolved in a non-aqueous liquid phase of an organic solvent.

12. The method for the production of chemically derivatized nanocellulose according to claim 1 , wherein the acylation agent is an anhydride of a carboxylic acid.

13. The method according to claim 1 , wherein the precursor cellulosic material is a suspension of precursor cellulosic material in a liquid phase, said liquid phase being a non-aqueous phase.

14. The method according to claim 1 , wherein the chemically derivatizing composition is a liquid chemically derivatizing composition providing for essentially the entire liquid comprised in the liquid reaction mixture.

15. The method for the production of chemically derivatized nanocellulose according to claim 1 , comprising the steps of:

a. contacting a precursor cellulosic material which is a chemically unmodified nanocellulose with a chemically derivatizing composition to form a liquid reaction mixture,

b. chemically reacting the formed liquid reaction mixture, and

c. subjecting the formed liquid reaction mixture to microfluidisation,

wherein the steps b. and c. are carried out simultaneously, and

wherein the chemically derivatizing composition is a liquid chemically derivatizing composition comprising a acylating agent suspended or dissolved in a non-aqueous liquid phase of an organic solvent, and the liquid phase provides for essentially the entire liquid comprised in the liquid reaction mixture.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 047552 FRAME 0665. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF THE ASSIGNOR'S INTEREST. Recorded Aug 17, 2022
From: WILLIAMS, RHODRI; ENGLISH, ROBERT; HEATON, JOHN
To: SAPPI NETHERLANDS SERVICES B.V.
Reel/Frame 061203/0546 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2018
From: WILLIAMS, RHODRI; ENGLISH, ROBERT; HEATON, JOHN
To: SAPPI NETHERLANDS SERVICES B.V.
Reel/Frame 047552/0665 →
Priority Claims (1)
EP 16171449 · May 25, 2016 · regional
Continuity (1)
Related Publication 20200317821A1 · Oct 8, 2020
Cited By (3)
US 12,325,841 US 12,545,864 US 12,545,866