IP Library Granted Patent US 12,291,599
Granted Patent B2
US 12,291,599 · App. 17/662,211 · Granted May 6, 2025

Semi-crystalline polyester polyol and method of making the same

Inventors: Brian W. Carlson (Woodbury, MN); Justin Kaffenberger (Circle Pines, MN); Alan R. Nahkala (Stillwater, MN)
Assignee: H.B. Fuller Company
C08G63/52C08G18/36C08G18/7692C08G63/12C08G63/20C08L75/14C09J7/38C09J175/14C09J2475/00
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 12,291,599
App. No.
17/662,211
Granted
May 6, 2025
Kind
B2
Abstract

Disclosed is a semi-crystalline polyester polyol having an acid number less than 4 and derived from a saturated fatty component having a hydroxyl number less than 2, the saturated fatty component being selected from the group consisting of saturated fatty acid, saturated fatty acid ester, saturated oil, and combinations thereof, polyhydric alcohol that includes at least three hydroxyl groups, and a dibasic acid.

Claims (34)

1. A semi-crystalline polyester polyol comprising:

the reaction product of

a saturated fatty component having a hydroxyl number less than 2, the saturated fatty component being selected from the group consisting of saturated fatty acid, saturated fatty acid ester, saturated oil, and combinations thereof,

a polyhydric alcohol comprising at least three hydroxyl groups, and

a dibasic acid,

the semi-crystalline polyester polyol being solid at room temperature, and having an acid number of less than 4 and a hydroxyl number of from 10 to 110.

2. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has an average hydroxyl functionality of from to 1.5 to 2.5.

3. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol exhibits a heat of fusion of at least 25 Joules per gram.

4. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol exhibits a heat of fusion of at least 50 Joules per gram.

5. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol exhibits a peak melt temperature of at least 30° C.

6. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol exhibits a peak crystallization temperature of at least 30° C.

7. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol exhibits a peak crystallization temperature of at least 35° C.

8. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 20 to 45.

9. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has an acid number of no greater than 2.

10. The semi-crystalline polyester polyol of claim 1 , wherein the dibasic acid is selected from the group consisting of succinic acid, adipic acid, suberic acid, sebacic acid, dodecanedioic acid, terephthalic acid, phthalic acid, phthalic anhydride, and combinations thereof.

11. The semi-crystalline polyester polyol of claim 1 , wherein the polyhydric alcohol is a tetraol.

12. The semi-crystalline polyester polyol of claim 1 , wherein the fatty component has an Iodine Value no greater than 50.

13. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol is further derived from monomeric diol.

14. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 10 to 110 and an acid number no greater than 2.

15. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 10 to 110 and an acid number no greater than 2, and exhibits a heat of fusion of at least 50 Joules per gram.

16. The semi-crystalline polyester polyol of claim 1 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 20 to 45 and an acid number less than 1, and exhibits a heat of fusion of at least 50 Joules per gram.

17. A semi-crystalline polyester polyol comprising:

a second reaction product of a dibasic acid and a first reaction product, the first reaction product being derived from

a saturated fatty component that has a hydroxyl number less than 2, the saturated fatty component being selected from the group consisting of saturated fatty acid, saturated fatty acid ester, saturated oil, and combinations thereof, and

polyhydric alcohol comprising at least three hydroxyl groups,

the semi-crystalline polyester polyol being solid at room temperature and having an acid number of less than 4.

18. The semi-crystalline polyester polyol of claim 17 , wherein the saturated fatty component is a saturated fatty acid ester, a saturated oil, or a combination thereof, and the first reaction product is a transesterification product resulting from the transesterification of the saturated fatty component with the polyhydric alcohol.

19. The semi-crystalline polyester polyol of claim 17 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 10 to 110.

20. The semi-crystalline polyester polyol of claim 17 , wherein the semi-crystalline polyester polyol has a hydroxyl number of from 20 to 45.

21. The semi-crystalline polyester polyol of claim 17 , wherein the semi-crystalline polyester polyol exhibits a heat of fusion of at least 25 Joules per gram.

22. A method of making a semi-crystalline polyester polyol, the method comprising:

reacting a saturated fatty component that has a hydroxyl number less than 2, the saturated fatty component being selected from the group consisting of saturated fatty acid, saturated fatty acid ester, saturated oil, and combinations thereof, and a polyhydric alcohol that includes at least three hydroxyl groups to form a first reaction product; and

reacting the first reaction product with a dibasic acid to form a solid semi-crystalline polyester polyol having an acid number of less than 4.

23. The method of claim 22 , wherein the saturated fatty component comprises an ester and the method comprises transesterifying the ester with the polyhydric alcohol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2024
From: CARLSON, BRIAN W.; KAFFENBERGER, JUSTIN; NAHKALA, ALAN R.
To: H.B. FULLER COMPANY
Reel/Frame 068932/0327 →
SECURITY INTEREST Recorded Feb 16, 2023
From: H.B. FULLER COMPANY; H.B. FULLER CONSTRUCTION PRODUCTS INC.; ADCO PRODUCTS, LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 062775/0944 →
Continuity (2)
Provisional Application 63201575 · May 5, 2021
Related Publication 20220356300A1 · Nov 10, 2022
References Cited (37)
US 3714090A · Lasher · 1973 [cited by examiner]
US 3963699A · Rizzi et al. · 1976 [cited by applicant]
US 4469635A · Peterson · 1984 [cited by applicant]
US 4624869A · De Graaf · 1986 [cited by applicant]
US 4740567A · Schmidt · 1988 [cited by applicant]
US 4798859A · Hohlein et al. · 1989 [cited by applicant]
US 5349041A · Blum · 1994 [cited by examiner]
US 5387642A · Blum · 1995 [cited by examiner]
US 5480667A · Corrigan et al. · 1996 [cited by applicant]
US 5490995A · Corrigan · 1996 [cited by applicant]
US 5527866A · Corrigan et al. · 1996 [cited by applicant]
US 5538670A · Sharma · 1996 [cited by applicant]
US 5624676A · Mackey et al. · 1997 [cited by applicant]
US 5958594A · Hisanaga et al. · 1999 [cited by applicant]
US 5959067A · Bakker et al. · 1999 [cited by applicant]
US 7098291B2 · Brinkman · 2006 [cited by applicant]
US 7374779B2 · Chen et al. · 2008 [cited by applicant]
US 8070833B2 · Murphy · 2011 [cited by applicant]
US 8157873B2 · Murphy et al. · 2012 [cited by applicant]
US 8333905B1 · Kurth et al. · 2012 [cited by applicant]
US 9334347B2 · DiBiase et al. · 2016 [cited by applicant]
US 20060182957A1 · Simmons · 2006 [cited by applicant]
US 20130131222A1 · Gross · 2013 [cited by applicant]
US 20140275310A1 · Adkins et al. · 2014 [cited by applicant]
US 20170002134A1 · Smits · 2017 [cited by examiner]
US 20170008997A1 · Honcoop · 2017 [cited by examiner]
US 20170190829A1 · Tian · 2017 [cited by applicant]
US 20180305597A1 · Yao · 2018 [cited by applicant]
US 20200055982A1 · Wu et al. · 2020 [cited by applicant]
US 20200148817A1 · Terwillegar et al. · 2020 [cited by applicant]
CA 888282 · 1971 [cited by applicant]
CN 103772675 · 2014 [cited by applicant]
EP 4261240 · 2022 [cited by applicant]
GB 2278350 · 1994 [cited by applicant]
KR 20110073975 · 2011 [cited by applicant]
WO WO2018005538 · 2018 [cited by applicant]
WO WO2003029182 · 2020 [cited by applicant]