IP Library Patent Application 15812408
Patent Application
App. No. 15/812,408

ALKOXYLATION OF LIGNINS

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Patent No.
US None
App. No.
15/812,408
Abstract

Disclosed is a method comprising: a) dispersing lignin into an alcohol-containing compound having a boiling point in the range of 120° C. to 300° C. to form a lignin dispersion; and b) contacting the lignin dispersion with an alkylene carbonate, optionally in the presence of a basic compound, at a temperature in the range of from 120° C. to 200° C. and a period of time in the range of from 0.25 hours to 24 hours to form an alkoxylated lignin dispersion.

Claims (18)

1 . A method comprising:

a) dispersing lignin into an alcohol-containing compound having a boiling point in the range of 120° C. to 300° C. to form a lignin dispersion; and

b) contacting the lignin dispersion with an alkylene carbonate, optionally in the presence of a basic compound, at a temperature in the range of from 120° C. to 200° C. and a period of time in the range of from 0.25 hours to 24 hours to form an alkoxylated lignin dispersion.

2 . A method in accordance with claim 1 , further comprising:

c) removing 40 weight percent to 90 weight percent of the alcohol-containing compound from the alkoxylated lignin dispersion.

3 . A method in accordance with claim 1 wherein the lignin is selected from the group consisting of lignosulfonates, kraft lignins, pyrolytic lignins, organosolv lignins, soda-ash lignins, steam explosion lignins, dilute acid lignins, biorefinery lignins, and combinations thereof.

4 . A method in accordance with claim 1 wherein the alkylene carbonate is selected from the group consisting of ethylene carbonate, propylene carbonate, and combinations thereof

5 . A method in accordance with claim 1 wherein the alcohol-containing compound is selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, glycerol, dipropylene glycol, dimethoxy glycol, and combinations thereof.

6 . A method in accordance with claim 1 wherein the lignin dispersion has a lignin to alcohol-containing compound weight ratio in the range of from 1:0.3 to 1:6.

7 . A method in accordance with claim 1 wherein the lignin is dispersed into the alcohol-containing compound over a period of time from 0.25 hours to 24 hours at a temperature in the range of from 25° C. to 150° C.

8 . A method in accordance with claim 1 wherein the lignin dispersion is present in step b) in the range of from 10 weight percent to 80 weight percent based on the total weight of components present in step b).

9 . A method in accordance with claim 1 wherein the alkylene carbonate is present in step b) in the range of from 20 weight percent to 90 weight percent, based on the total weight of components present in step b).

10 . A method in accordance with claim 1 wherein the basic compound is selected from the group consisting of sodium hydroxide, sodium carbonate, potassium hydroxide, potassium carbonate, lithium hydroxide, calcium hydroxide, calcium carbonate, melamine, triethyl amine, triethanol amine, hexamethylene diamine, ethylene diamine, diethanol amine, and combinations thereof.

11 . A method in accordance with claim 1 wherein the basic compound is present in step b) in the range of from 0.25 weight percent to 5 weight percent, based on the total weight of components present in step b).

12 . A method in accordance with claim 1 wherein the alkoxylated lignin dispersion further comprises from 5 weight percent to 30 weight percent of a polyisocyanate-reactive compound.

13 . A method in accordance with claim 12 wherein the polyisocyanate-reactive compound is selected from the group consisting of polyether polyols, polyester polyols, Mannich base polyols, and combinations thereof.

14 . A method in accordance with claim 1 wherein the alkoxylated lignin has a glass transition temperature in the range of from −10° C. to −80° C.

15 . A method in accordance with claim 2 wherein, after step c), the alkoxylated lignin dispersion has a viscosity at 70° C. in the range of from 0.1 Pa·s to 40 Pa·s.

Assignments (8)
RELEASE OF SECURITY INTEREST IN PATENTS (TERM LOAN) RECORDED AT REEL/FRAME 049741/0425 Recorded Mar 18, 2022
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: HEXION INC.
Reel/Frame 059435/0473 →
RELEASE OF SECURITY INTEREST IN PATENTS (ABL) RECORDED AT REEL/FRAME 049740/0770 Recorded Mar 18, 2022
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: HEXION INC.
Reel/Frame 059435/0490 →
PATENT SECURITY INTEREST (ABL) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049740/0770 →
PATENT SECURITY INTEREST (TERM LOAN) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049741/0425 →
SECURITY INTEREST Recorded Feb 2, 2018
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 044814/0825 →
SECURITY INTEREST Recorded Feb 2, 2018
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 044814/0920 →
SECURITY INTEREST Recorded Feb 2, 2018
From: HEXION INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 044814/0971 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2017
From: MAIORANA, ANTHONY; MADDIPATLA, MURTHY V.S.N.; VISWANATHAN, GANAPATHY
To: HEXION INC.
Reel/Frame 044122/0849 →