IP Library Granted Patent US 12,435,180
Granted Patent B2
US 12,435,180 · App. 17/852,469 · Granted Oct 7, 2025

Poly(3-hydroxyacid) polymers from long-chain epoxides and their uses related to hot melt adhesives

Inventors: Steven D. Gray (Wauwatosa, WI); Darius Deak (Wauwatosa, WI)
Assignee: Bostik SA
C08G63/08C08F283/004C08G63/912C09J167/04C08G2230/00C09J2301/302C09J2301/304C09J2467/00
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 12,435,180
App. No.
17/852,469
Granted
Oct 7, 2025
Kind
B2
Abstract

A macromolecule comprises a ring-opened polymerized product of β-lactone monomers of formula I: and having a structure of formula IA: wherein R 1 is an alkyl group having at least 8 carbon atoms. The macromolecule may be hydroxy-terminated, and may be copolymerized with other β-lactone monomers having different substituting groups and/or with higher lactone monomers. The macromolecule may be used as a reactant to form an alkoxysilane-terminated polymer, a polyurethane, or a (co)polyester, or may be used as an elastomeric midblock in a triblock copolymer having hard end blocks, such as polylactic acid. Such triblock systems demonstrate two discreet regions having properties similar to styrene block copolymers and are therefore suitable for use as hot melt or pressure-sensitive adhesives. In some embodiments, such triblock polymers may be entirely bio-sourced and compostable.

Claims (22)

1. A macromolecule comprising a ring-opened polymerized product of β-lactone monomers of formula I:

and higher lactone monomers of formula III:

wherein X=(CH 2 ) a , or

and having a structure of formula IIIB:

wherein: (1) R 2 is hydrogen or an alkyl or a substituted alkyl; (2) a is at least 3; (3) the total of m and p is between 10 and 10,000; (4) the macromolecule is a diol and is hydroxy-terminated and R 1 is an alkyl having at least 8 carbon atoms; and (5) D is a hydrocarbon residue from a diol initiator.

2. The macromolecule of claim 1 , wherein the diol initiator comprises 1,4-benzenedimethanol.

3. The macromolecule of claim 1 , wherein the diol initiator comprises a polymer.

4. A method for making a silane-modified, moisture curable oligomer or polymer comprising reacting the macromolecule claim 1 with a siloxide to form an alkoxysilane-terminated oligomer or polymer.

5. A method for making a polyurethane comprising reacting the macromolecule of claim 1 with an isocyanate.

6. A method for making a (co)polyester comprising reacting the macromolecule of claim 1 with a diacid or diester.

7. A triblock copolymer having an A:B:A backbone, wherein block B comprises a residue of the macromolecule of claim 1 and block A is a residue of a polymer selected from the group consisting of polylactic acid, polycaprolactone, polyhydroxybutyrates, or polyamides or copolymers thereof.

8. The triblock copolymer of claim 7 , wherein block A is amorphous and has a melting temperature (T m ) of above 60° C.

9. The triblock copolymer of claim 7 , wherein block A is immiscible with block B.

10. The triblock copolymer of claim 7 , wherein the triblock copolymer comprises 95 to 40 molar percent of the block B and 60 to 5 molar percent of the block A.

11. The triblock copolymer of claim 7 , wherein block A is a ring-opened polymerized product of lactide.

12. A hot melt adhesive comprising the triblock copolymer of claim 7 .

13. The hot melt adhesive of claim 12 further comprising a tackifier, a plasticizer, and, optionally, other additives.

14. A pressure sensitive adhesive comprising the triblock copolymer of claim 7 .

15. The pressure sensitive adhesive of claim 14 further comprising a tackifier, a plasticizer, and, optionally, other additives.

16. The macromolecule of claim 1 , wherein the β-lactone monomers of formula I are non-functionalized.

17. The macromolecule of claim 1 , wherein the β-lactone monomers of formula I are produced by carbonylation of an epoxide.

18. The macromolecule of claim 3 , wherein the polymer is selected from the groups consisting of polyethylene glycol and polypropylene glycol.

Assignments (2)
CHANGE OF ADDRESS Recorded Jul 30, 2025
From: BOSTIK SA
To: BOSTIK SA
Reel/Frame 072277/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2022
From: GRAY, STEVEN D.; DEAK, DARIUS
To: BOSTIK SA
Reel/Frame 060561/0822 →
Continuity (2)
Provisional Application 63216031 · Jun 29, 2021
Related Publication 20230002549A1 · Jan 5, 2023
References Cited (29)
US 3021313A · Cox et al. · 1962 [cited by applicant]
US 5032671A · Harper · 1991 [cited by applicant]
US 5648452A · Schechtman et al. · 1997 [cited by applicant]
US 5994478A · Asrar · 1999 [cited by examiner]
US 8163824B2 · Okazaki et al. · 2012 [cited by applicant]
US 20070149724A1 · Pacetti et al. · 2007 [cited by applicant]
US 20080146775A1 · Uemori · 2008 [cited by examiner]
US 20100131064A1 · Redepenning · 2010 [cited by applicant]
US 20110287102A1 · Gunatillake · 2011 [cited by examiner]
US 20140275467A1 · Jamiolkowski · 2014 [cited by examiner]
US 20140357410A1 · Chou · 2014 [cited by examiner]
US 20180155491A1 · Sookraj · 2018 [cited by examiner]
JP 2017025138A · 2017 [cited by examiner]
TW 201730229A · 2017 [cited by examiner]
WO WO9636656 · 1996 [cited by applicant]
WO WO9910404 · 1999 [cited by examiner]
WO WO0037119A1 · 2000 [cited by applicant]
WO WO0077072A1 · 2000 [cited by applicant]
WO WO2005061580A1 · 2005 [cited by examiner]
WO WO2013128175A1 · 2013 [cited by applicant]
WO WO2015021254A1 · 2015 [cited by examiner]
WO WO21210608A1 · 2021 [cited by applicant]
WO WO2021207394A1 · 2021 [cited by applicant]
WO WO2022040040A1 · 2022 [cited by applicant]
WO WO2022212124A1 · 2022 [cited by examiner]
ACS Sustainalbe Chemistry & Engineering; “Sustainable Triblock Copolymers as Tunable and Degradable Pressure Sensitive Adhesives”; Hee Joong Kim et al—Chem Eng. 2020, 8, pp. 12036-12044. [cited by applicant]
Macromolecules 2000, 33, pp. 4690-4698—“Renewable Long-Chain Fatty Acids for Production of Biodegradable Medium-Chain-Length Polyhdroxyalkanoates (mcl-PHAs) at Laboratory and Pilot Plant Scales”; Kellerhals et al. [cited by applicant]
Polymer Chemistry—Royal Society of Chemistry “Tuning thermal properties and microphase separation in aliphatic polyester ABA copolymers”—Journal—The Royal Society of Chemistry 2015 Poly Chem 2015 6, pp. 1445-1453. [cited by applicant]
Biomacromolecules 2005, 6, pp. 580-586—“Preparation and Properties of a Noval Class of Polyhydroxyalkanoate Copolymers”, Isao Noda, Phillip R. Green, Michael M. Satkowski and Lee A. Schechtman; 2005 American Chemical So… [cited by applicant]