IP Library Granted Patent US 12,202,942
Granted Patent B2
US 12,202,942 · App. 17/692,635 · Granted Jan 21, 2025

Functionalized silicone polymers and methods of making and using the same

Inventors: Charles Coburn (Vernon Hills, IL); Paul A. Bertin (Western Springs, IL)
Assignee: Wilmar Trading Pte Ltd.
C08G77/14C08G77/38C08G77/385C08G77/388
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Quick Facts
Patent No.
US 12,202,942
App. No.
17/692,635
Granted
Jan 21, 2025
Kind
B2
Abstract

Functionalized silicone polymers incorporating segments formed from medium-chain fatty acids are generally disclosed herein. Methods of using such compounds, for example, as surfactants, are also disclosed herein, as well as methods of making such compounds, for example, from medium-chain fatty acids derived from natural oils.

Claims (35)

1. A siloxane polymer of formula (I):

wherein:

each R 1 , R 2 , R 3 , and R 4 is independently a hydrogen atom, a C 1-14 hydrocarbyl group, or a C 1-14 hydrocarbyloxy group;

R x and R y are —(CH 2 ) n C(═O)—R 5 ;

each R 5 is independently —O—R 6 ;

each R 6 , is independently C 1-30 alkyl, C 2-30 alkenyl, or C 1-401 heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R z ;

R z is a halogen atom, —OH, —NH 2 , —SH, or C 6-14 aryl, wherein any two-OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group;

each R 6 is independently C 1-12 alkyl, which is substituted by one or more halogen atoms;

each n is independently an integer ranging from 9 to 17; and

k is independently an integer ranging from 5 to 5000.

2. The siloxane polymer of claim 1 , wherein each R 6 is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl.

3. The siloxane polymer of claim 1 , wherein each R 6 is independently C 3-401 oxyalkyl.

4. The siloxane polymer of claim 3 , wherein each R 6 is independently —(CH 2 —CH 2 —O) w —CH 3 , wherein w is an integer ranging from 1 to 200.

5. A siloxane polymer comprising a plurality of constitutional units, wherein the plurality of constitutional units comprises:

(a) constitutional units of formula (II):

and

(b) constitutional units of formula (III):

wherein:

each R 1 and R 2 is independently a hydrogen atom, a C 3-101 oxyalkyl group, or a C 1-14 hydrocarbyl group, which is optionally substituted one or more times by halogen atoms;

each R 3 and R 4 is independently a hydrogen atom, —(CH 2 ) n C(═O)—R 5 , a C 3-101 oxyalkyl group, or a C 1-14 hydrocarbyl group, which is optionally substituted one or more times by halogen atoms, wherein, for each constitutional unit of formula (III), at least one of R 3 and R 4 is —(CH 2 ) n C(═O)—R 5 ;

each R 5 is independently —O—R 6 , —NH—R 7 , or —N(R 8 ) (R 9 );

each R 8 and R 9 is independently C 1-30 alkyl, C 2-30 alkenyl, or C 1-401 heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R x ;

each R 6 is independently —(CH 2 ) x —CH(O)CH 2 , wherein x is an integer ranging from 1 to 12;

R x is a halogen atom, —OH, —NH 2 , —SH, or C 6-14 aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; and

each n is independently an integer ranging from 9 to 17;

wherein when R 5 is independently —NH—R 7 , R 7 is a moiety of formula (IV):

-G 3 -N + —(R 11 )(R 12 )-G 4 -R 13   (IV)

wherein:

G 3 is C 1-12 alkylene;

G 4 is C 1-6 alkylene;

R 11 and R 12 are independently a hydrogen atom or C 1-20 alkyl; and

R 13 is a hydrogen atom or a phenyl moiety.

6. The siloxane polymer of claim 5 , wherein each R 5 is independently —O—R 6 .

7. The siloxane polymer of claim 5 , wherein the constitutional units of formula (II) and the constitutional units of formula (III) together make up at least 60% by weight of the constitutional units in the siloxane polymer.

8. The siloxane polymer of claim 5 , wherein the numerical ratio of constitutional units of formula (II) to constitutional units of formula (III) in the siloxane polymer ranges from 1:5 to 5:1, or from 1:4 to 4:1, or from 1:3 to 3:1, or from 1:2 to 2:1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2022
From: ELEVANCE RENEWABLE SCIENCES, INC.
To: WILMAR TRADING PTE. LTD.
Reel/Frame 060175/0722 →
Continuity (5)
Continuation 16573300 · Sep 17, 2019
Provisional Application 62732324 · Sep 17, 2018
Provisional Application 62732408 · Sep 17, 2018
Provisional Application 62732416 · Sep 17, 2018
Related Publication 20220204703A1 · Jun 30, 2022
References Cited (29)
US 5063044A · Kohl et al. · 1991 [cited by applicant]
US 5981680A · Petroff et al. · 1999 [cited by applicant]
US 6051216A · Barr et al. · 2000 [cited by applicant]
US 6388042B1 · O'Lenick, Jr. · 2002 [cited by applicant]
US 6727340B1 · O'Lenick, Jr. · 2004 [cited by applicant]
US 7635581B2 · Ferenz et al. · 2009 [cited by applicant]
US 8957121B2 · Schiller · 2015 [cited by examiner]
US 20040171783A1 · Cook et al. · 2004 [cited by applicant]
US 20080063879A1 · Lin et al. · 2008 [cited by applicant]
US 20150274893A1 · O'Lenick · 2015 [cited by applicant]
US 20160311982A1 · Sakurai · 2016 [cited by applicant]
US 20170355721A1 · Frampton et al. · 2017 [cited by applicant]
US 20180118891A1 · Ando · 2018 [cited by applicant]
US 20180201795A1 · Hed et al. · 2018 [cited by applicant]
JP 2018070790 · 2018 [cited by applicant]
U.S. Appl. No. 17/499,058, Non-Final Office Action dated Dec. 29, 2022, 12 pages. [cited by applicant]
U.S. Appl. No. 16/573,293, Non-Final Office Action dated Mar. 3, 2021, 8 pages. [cited by applicant]
U.S. Appl. No. 16/573,293, Notice of Allowance dated Jul. 14, 2021, 9 pages. [cited by applicant]
U.S. Appl. No. 16/573,300, Non-Final Office Action dated Sep. 17, 2021, 7 pages. [cited by applicant]
U.S. Appl. No. 16/573,300, Non-Final Office Action dated Mar. 16, 2021, 8 pages. [cited by applicant]
U.S. Appl. No. 16/573,300, Notice of Allowance dated Jan. 20, 2022, 6 pages. [cited by applicant]
U.S. Appl. No. 16/573,300, “Supplemental Notice of Allowability” dated Feb. 4, 2022, 3 pages. [cited by applicant]
Application No. PCT/US2019/051446, International Preliminary Report on Patentability dated Mar. 25, 2021, 6 pages. [cited by applicant]
Application No. PCT/US2019/051446, International Search Report and Written Opinion dated Jan. 3, 2020, 9 pages. [cited by applicant]
Shepperson et al., “Polyphilic Multicomponent Dimers with Perfluorinated Cores”, Molecular Crystals and Liquid Crystals, vol. 411, 2004, pp. 185-191. [cited by applicant]
Application No. EP19863876.9 , Extended European Search Report, dated May 6, 2022, 7 pages. [cited by applicant]
Saghian et al., “Silicon-Containing Condensation Polymers Derived from Long-Chain Fatty Acids”, Journal of Macromolecular Science: Part A—Chemistry, vol. 9, No. 3, May 5, 1975, pp. 341-356. [cited by applicant]
U.S. Appl. No. 17/499,058, “Final Office Action”, dated Apr. 26, 2023, 6 pages. [cited by applicant]
U.S. Appl. No. 17/499,058, “Notice of Allowance”, dated Aug. 11, 2023, 12 pages. [cited by applicant]
Cited By (1)
US 12,606,677