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US-12617896-B2 - Ionomer polyamides, primers, articles, and methods of making same

US12617896B2US 12617896 B2US12617896 B2US 12617896B2US-12617896-B2

Abstract

Ionomer polyamides membranes are provided, including a reaction product of a polymerizable composition including a first diacid that is a dimer acid; an ionomer component; a first diamine that is an oxyalkylene diamine; at least one second diamine comprising a primary diamine and/or a secondary diamine; and optionally at least one second diacid. The ionomer component is an ionomer diacid, an ionomer diester, or an ionomer diamine. The present disclosure also provides primers containing the ionomer polyamide dispersed in water and/or a lower alcohol. Further, articles are provided including a substrate and the ionomer polyamide or the primer disposed on the substrate. Methods are additionally provided, including methods of making an ionomer polyamide and making an article.

Inventors

  • Rajdeep S. Kalgutkar
  • David T. Amos
  • Tianyu Wu
  • Jeffrey A. Peterson
  • Becky A. Jetto

Assignees

  • 3M INNOVATIVE PROPERTIES COMPANY

Dates

Publication Date
20260505
Application Date
20221031

Claims (20)

  1. 1 . An ionomer polyamide comprising a reaction product of a polymerizable composition comprising: a) a first diacid that is a dimer acid; b) an ionomer component that is an ionomer diacid, an ionomer diester, and/or an ionomer diamine; c) a first diamine that is an oxyalkylene diamine; d) at least one second diamine comprising a primary diamine and/or a secondary diamine; and e) optionally at least one second diacid, wherein a mole fraction of the dimer acid is 0.40 to 0.99, a mole fraction of the ionomer component is 0.01 to 0.20, and a mole fraction of the at least one second diacid is 0 to 0.60, each based on the total moles of a combination of the dimer acid, the at least one second diacid, and any ionomer diacid or diester used to form the ionomer polyamide; and wherein a mole fraction of the oxyalkylene diamine is 0.005 to 0.10 and a mole fraction of the at least one second diamine is 0.90 to 0.995, each based on the total moles of a combination of the oxyalkylene diamine, the at least one second diamine, and any ionomer diamine used to form the ionomer polyamide.
  2. 2 . The ionomer polyamide of claim 1 , wherein the oxyalkylene diamine comprises each of an ethylene oxide and a propylene oxide.
  3. 3 . The ionomer polyamide of claim 2 , wherein the ionomer polyamide is acid- or amine-terminated.
  4. 4 . The ionomer polyamide of claim 1 , wherein the at least one second diamine comprises an aliphatic diamine and a cycloaliphatic diamine.
  5. 5 . The ionomer polyamide of claim 1 , wherein the at least one second diamine is of the Formula (III): R5-NH-R6-NH—R5 (III); wherein R5 is independently selected from a linear or branched alkyl, a cycloalkyl, an aryl, a heteroalkyl, a heteroaryl, a hydrogen atom with the proviso that both R5s are not hydrogen atoms, or the R5 groups are alkylene or branched alkylene and form a heterocyclic compound; and wherein R6 is an alkylene, a branched alkylene, a cycloalkylene, a substituted or unsubstituted arylene, or a heteroalkylene.
  6. 6 . The ionomer polyamide of claim 1 , wherein the dimer acid has a number average molecular weight of between 300 g/mol and 1400 g/mol.
  7. 7 . The ionomer polyamide of claim 1 , wherein the polymerizable composition lacks a diol.
  8. 8 . The ionomer polyamide of claim 1 , wherein the ionomer polyamide is of the structure of Formula (I) or Formula (II): wherein R1 is independently selected from a residue of the dimer acid, a residue of the ionomer diacid or diester, or a residue of any other diacid monomers; wherein R2 is independently selected from a residue of a primary diamine or a secondary diamine; wherein R3 is independently selected from an alkylene group or an arylene group; and wherein R4 is independently selected from H, an alkyl group, an alkenyl group, an aryl group, a cycloalkyl group, or two R4 groups are alkylene or branched alkylene and form a heterocyclic compound.
  9. 9 . A primer comprising up to 20 percent by weight of the ionomer polyamide of claim 1 .
  10. 10 . The primer of claim 9 , wherein the ionomer polyamide is dispersed in a solvent comprising 80-90 percent by weight water, 10-20 percent by weight of a C2-C4 aliphatic alcohol, and optionally a pH adjuster.
  11. 11 . The primer of claim 9 , wherein the ionomer polyamide is dispersed in water.
  12. 12 . The primer of claim 9 , wherein the ionomer polyamide is acid- or amine-terminated and the primer has a pH of 2-6 or 8-11.
  13. 13 . An article comprising a substrate and a layer of the ionomer polyamide of claim 1 disposed on a major surface of the substrate.
  14. 14 . The article of claim 13 , further comprising an adhesive disposed on a major surface of the layer of the ionomer polyamide comprising a polymer comprising at least one pendant carboxylic acid group.
  15. 15 . The article of claim 13 , wherein the layer of the ionomer polyamide has an average thickness of less than 1 micrometer, less than 0.5 micrometers, or less than 0.25 micrometers.
  16. 16 . An article comprising a substrate and a layer of the primer of claim 9 disposed on a major surface of the substrate.
  17. 17 . The article of claim 13 , wherein the substrate comprises a polar polymeric material.
  18. 18 . A method of making an ionomer polyamide, the method comprising reacting components of a polymerizable composition comprising: a) a first diacid that is a dimer acid; b) an ionomer component that is an ionomer diacid, an ionomer diester, and/or an ionomer diamine; c) a first diamine that is an oxyalkylene diamine; d) at least one second diamine comprising a primary diamine and/or a secondary diamine; and e) optionally at least one second diacid, wherein a mole fraction of the dimer acid is 0.40 to 0.99, a mole fraction of the ionomer component is 0.01 to 0.20, and a mole fraction of the at least one second diacid is 0 to 0.60, each based on the total moles of a combination of the dimer acid, the at least one second diacid used to form the ionomer polyamide, and any ionomer diacid or diester, and wherein a mole fraction of the oxyalkylene diamine is 0.005 to 0.10 and a mole fraction of the at least one second diamine is 0.70 to 0.995, each based on the total moles of a combination of the oxyalkylene diamine, the at least one second diamine, and any ionomer diamine used to form the ionomer polyamide.
  19. 19 . A method of making an article comprising: coating the primer of claim 9 on a major surface of a substrate; and orienting the substrate.
  20. 20 . The method of claim 19 , further comprising at least one of heating or drying the primer, thereby obtaining a layer of the ionomer polyamide having an average thickness of less than 1 micrometer, less than 0.5 micrometers, or less than 0.25 micrometers.

Description

FIELD The present disclosure generally relates to ionomer polyamides. SUMMARY In a first aspect, an ionomer polyamide is provided. The ionomer polyamide includes a reaction product of a polymerizable composition including a) first diacid that is a dimer acid; b) an ionomer component that is an ionomer diacid, an ionomer diester, and/or an ionomer diamine; c) a first diamine that is an oxyalkylene diamine; d) at least one second diamine comprising a primary diamine and/or a secondary diamine; and e) optionally at least one second diacid. A mole fraction of the dimer acid is 0.40 to 0.99, a mole fraction of the ionomer component is 0.01 to 0.20, and a mole fraction of the at least one second diacid is 0 to 0.60, each based on the total moles of a combination of the dimer acid, the at least one second diacid, and any ionomer diacid or diester used to form the ionomer polyamide. A mole fraction of the oxyalkylene diamine is 0.005 to 0.10 and a mole fraction of the at least one second diamine is 0.70 to 0.995, each based on the total moles of a combination of the oxyalkylene diamine, the at least one second diamine, and any ionomer diamine used to form the ionomer polyamide. In a second aspect, a primer is provided. The primer includes up to 20 percent by weight of the ionomer polyamide according to the first aspect. In a third aspect, an article is provided. The article includes a substrate and a layer of the ionomer polyamide according to the first aspect disposed on a major surface of the substrate. In a fourth aspect, another article is provided. The article includes a substrate and a layer of the primer according to the second aspect disposed on a major surface of the substrate. In a fifth aspect, a method of making an ionomer polyamide is provided. The method includes reacting components of a polymerizable composition including: a) first diacid that is a dimer acid; b) an ionomer component that is an ionomer diacid, an ionomer diester, and/or an ionomer diamine; c) a first diamine that is an oxyalkylene diamine; d) at least one second diamine comprising a primary diamine and/or a secondary diamine; and e) optionally at least one second diacid. A mole fraction of the dimer acid is 0.40 to 0.99, a mole fraction of the ionomer component is 0.01 to 0.20, and a mole fraction of the at least one second diacid is 0 to 0.60, each based on the total moles of a combination of the dimer acid, the at least one second diacid, and any ionomer diacid or diester used to form the ionomer polyamide. A mole fraction of the oxyalkylene diamine is 0.005 to 0.10 and a mole fraction of the at least one second diamine is 0.70 to 0.995, each based on the total moles of a combination of the oxyalkylene diamine, the at least one second diamine, and any ionomer diamine used to form the ionomer polyamide. In a sixth aspect, a method of making an article is provided. The method includes: coating the primer according to the second aspect on a major surface of a substrate; and orienting the substrate. The above summary of the present disclosure is not intended to describe each disclosed embodiment or every implementation of the present disclosure. The description that follows more particularly exemplifies illustrative embodiments. In several places throughout the application, guidance is provided through lists of examples, which examples may be used in various combinations. In each instance, the recited list serves only as a representative group and should not be interpreted as an exclusive list. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic cross-sectional view of an exemplary article according to the present disclosure. FIG. 2 is a schematic cross-sectional view of another exemplary article according to the present disclosure. FIG. 3 is a flow chart of an exemplary method of making an ionomer polyamide according to the present disclosure. FIG. 4 is a flow chart of an exemplary method of making an article according to the present disclosure. While the above-identified figures set forth various embodiments of the disclosure, other embodiments are also contemplated, as noted in the description. In all cases, this disclosure presents the invention by way of representation and not limitation. The figures are not necessarily to scale. Like numbers used in the figures refer to like components. However, it will be understood that the use of a number to refer to a component in a given figure is not intended to limit the component in another figure labeled with the same number. DETAILED DESCRIPTION Glossary The thickness of a layer (coating, substrate, adhesive, etc.) should be understood to be its smallest dimension. It is generally referred to as the “z” dimension and refers to the distance between the major surfaces of the layer. As used herein, the terms “hardenable” refers to a material that can be cured or solidified, e.g., by heating to remove solvent, heating to cause polymerization, chemical crosslinking, radiation-induced pol