IP Library Patent Application 18681354
Patent Application
App. No. 18/681,354

REDUCED VISCOSITY COMPOSITIONS CONTAINING POLYAMIDEIMIDE POLYMERS

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Patent No.
US None
App. No.
18/681,354
Abstract

Compositions based on low toxicity solvents, in particular coating formulations, having reduced viscosity are disclosed. The compositions contain polyamideimide polymers having well-defined molecular weight distribution.

Claims (64)

1 . An aromatic polyamic acid/polyamideimide polymer [Polymer (PAI)] which comprises recurring units, more than 50 mol % of said recurring units, [recurring units (R PAI )], are chosen from the group consisting of:

wherein:

the symbol → in each formula denotes isomerism so that, in any recurring unit within the aromatic polyamic acid structure, the groups to which the arrows point may exist as shown or in an interchanged position;

Ar is an aromatic tetravalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with X being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5;

R is an aromatic divalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with Y being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5,

wherein said aromatic polyamic acid/polyamideimide polymer has a molecular weight distribution, M w /M n , from 2.00 to 3.40, and

wherein the recurring units (R PAI ) are chosen from the group consisting of units (i), (ii) and (iii):

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (i-a) will be understood to represent the 1,3 and the 1,4 polyamide-amic acid configurations;

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (ii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations;

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (iii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations; and

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (iii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations.

2 . (canceled)

3 . The Polymer (PAI) of claim 1 , in which the recurring units (R PAI ) are recurring units (i) or a mix of recurring units (ii) and (iii).

4 . The Polymer (PAI) of claim 1 , wherein the Polymer (PAI) comprises more than 90 mol % of recurring units (R PAI ).

5 . The Polymer (PAI) of anyone of claim 1 , wherein the Polymer (PAI) has an acid number of less than 50, measured as milligrams of KOH/gram of polymer.

6 . The Polymer (PAI) of claim 1 , wherein the Polymer (PAI) has a molecular weight distribution M w /M n from 2.50 to 3.40, preferably from 2.80 to 3.40.

7 . A process for the manufacture of Polymer (PAI), the process comprising a polycondensation reaction between at least an aromatic polycarboxylic acid halide monomer and at least an aromatic diamine in the presence of an excess of the aromatic polycarboxylic acid halide monomer with respect to the aromatic diamine monomer.

8 . The process of claim 7 , wherein the aromatic polycarboxylic acid halide monomer is present in an excess of at least 5 mol % with respect to the equimolar concentration of the aromatic diamine monomer, preferably in an excess of 10 to 15 mol % with respect to the equimolar concentration of the aromatic diamine monomer.

9 . A composition comprising a Polymer (PAI) and a non-toxic solvent, [solvent (S)].

10 . The composition according to claim 9 , wherein the solvent (S) is selected from the group consisting of at least one of the following: N-butylpyrrolidone, N-acetylpyrrolidone, methyl-5-(dimethylamino)-2-methyl-5-oxopentanoate, dimethyldecanamide, 1,3-Dimethyl-2-imidazolidinone (DMI), 3-methoxy-N,N-dimethylpropanamide, 2-hydroxy-N,N-dimethylpropanamide, isosorbide dimethylether, 2-isobutyl-2-methyl-1,3-dioxolane-4-methanol, gamma-valerolactone, a mixture including ethyl lactate and an ethyl ester derived from soya bean oil or corn oil, dimethyl glutarate, dimethyl succinate, dimethyl adipate, mixtures of dimethyl glutarate, dimethyl succinate, dimethyl adipate and dimethyl 2-methylglutarate.

11 . The composition according to claim 9 , wherein the solvent (S) is selected from the group consisting of at least one of N-butylpyrrolidone and methyl-5-(dimethylamino)-2-methyl-5-oxopentanoate.

12 . The composition according to claim 9 , wherein the composition comprises less than 5.0 wt %, less than 2.0 wt %, less than 1.0 wt % of any solvent different from the solvent (S).

13 . The composition according to claim 9 , further comprising 10 to 45 wt % of the Polymer (PAI) with respect to the total weight of the composition.

14 . The process of claim 7 , further comprising manufacturing an article comprising coating the Polymer (PAI) on a substrate.

15 . The process of claim 14 , further comprising the step of curing the Polymer (PAI) by heating at a temperature between 12° and 400° C.

16 . The process of claim 7 , further comprising forming an article comprising the Polymer (PAI).

17 . The process of claim 16 , wherein the article is a wire, a cookware article, a battery, a flexible electronic component, an oil or gas pipe.

18 . (canceled)

19 . The process of claim 7 , wherein the Polymer (PAI) comprises recurring units, more than 50 mol % of said recurring units, [recurring units (R PAI )], are chosen from the group consisting of:

wherein:

the symbol → in each formula denotes isomerism so that, in any recurring unit within the aromatic polyamic acid structure, the groups to which the arrows point may exist as shown or in an interchanged position;

Ar is an aromatic tetravalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with X being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5;

R is an aromatic divalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with Y being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5,

wherein said Polymer (PAI) has a molecular weight distribution, M w /M n from 2.00 to 3.40, and

wherein the recurring units (R PAI ) are chosen from the group consisting of units (i), (ii) and (iii):

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (i-a) will be understood to represent the 1,3 and the 1,4 polyamide-amic acid configurations;

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (ii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations; and

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (iii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations.

20 . The composition of claim 9 , wherein the Polymer (PAI) comprises recurring units, more than 50 mol % of said recurring units, [recurring units (R PAI )], are chosen from the group consisting of:

wherein:

the symbol → in each formula denotes isomerism so that, in any recurring unit within the aromatic polyamic acid structure, the groups to which the arrows point may exist as shown or in an interchanged position;

Ar is an aromatic tetravalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with X being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5;

R is an aromatic divalent group, which may comprise one or more than one aromatic ring, and which is preferably selected from the group consisting of:

with Y being selected from the group consisting of —O—, —C(O)—, —S—, —SO 2 —, —CH 2 —, —C(CF 3 ) 2 —, —(CF 2 ) n — with n=0, 1, 2, 3, 4 or 5,

wherein said Polymer (PAI) has a molecular weight distribution, M w /M n from 2.00 to 3.40, and

wherein the recurring units (R PAI ) are chosen from the group consisting of units (i), (ii) and (iii):

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (i-a) will be understood to represent the 1,3 and the 1,4 polyamide-amic acid configurations;

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (ii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations; and

and/or the corresponding imide-group containing recurring unit:

wherein the attachment of the two amide groups to the aromatic ring as shown in (iii-a) represent the 1,3 and the 1,4 polyamide-amic acid configurations.

Assignments (2)
CHANGE OF NAME Recorded Oct 14, 2025
From: SOLVAY SPECIALTY POLYMERS USA, LLC
To: SYENSQO SPECIALTY POLYMERS USA, LLC
Reel/Frame 073076/0851 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2024
From: TILFORD,, R. WILLIAM; PELLISSIER, JARROD; GALINAT DELPEH, SOPHIE; ARMISEN, SAMANTHA; BOCAHUT, ANTHONY
To: SOLVAY SPECIALTY POLYMERS USA, LLC
Reel/Frame 066495/0857 →