US2022348696A1PendingUtilityA1
Articles and methods related to labile crosslinking moieties
Est. expiryAug 19, 2040(~14.1 yrs left)· nominal 20-yr term from priority
C08F 8/50C08F 8/12C09D 133/00C08F 228/02C08F 230/08C08G 77/38C08F 30/08C09D 4/00C08F 130/08
72
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Articles and methods related to the manufacture of polymers containing labile crosslinking moieties are generally described.
Claims
exact text as granted — not AI-modified1 . A method comprising:
providing a structurally self-supporting material comprising a polymeric material crosslinked by a plurality of crosslinking moieties; exposing at least a portion of the structurally self-supporting material to H 2 O, thereby reacting at least a portion of the crosslinking moieties and converting at least a portion of the structurally self-supporting material to a non-structurally self-supporting material.
2 . The method of claim 1 , wherein providing the structurally self-supporting material comprises providing the structurally self-supporting material on a substrate.
3 . The method of claim 2 , wherein providing the structurally self-supporting material comprises three-dimensional (3D) printing the structurally self-supporting material on the substrate.
4 . The method of claim 1 , wherein the plurality of crosslinking moieties at least partially render the material structurally self-supporting.
5 . The method of claim 1 , wherein each of the crosslinking moieties comprise an acrylate.
6 . The method of claim 5 , wherein each of the crosslinking moieties comprise a methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, and/or derivatives thereof.
7 . The method of claim 1 , wherein each of the crosslinking moieties comprises a silyl-ether.
8 . The method of claim 1 , wherein reacting at least a portion of the crosslinking moieties comprises hydrolyzing at least a portion of the crosslinking moieties.
9 . The method of claim 1 , wherein the structurally self-supporting material has a Young's modulus between greater than or equal to 1 GPa and less than or equal to 5 GPa.
10 . The method of claim 1 , wherein the non-structurally self-supporting material has a Young's modulus between less than or equal to 1 GPa and greater than or equal to 0.01 GPa.
11 . The method of claim 1 , wherein exposing at least a portion of the structurally self-supporting material to H 2 O comprises at least partially submerging the structurally self-supporting material in water.
12 . The method of claim 1 , wherein exposing at least a portion of the structurally self-supporting material to H 2 O comprises exposing the structurally self-supporting material to moisture.
13 . The method of claim 1 , wherein exposing at least a portion of the structurally self-supporting material to H 2 O comprises exposing at least a portion of the structurally self-supporting material to H 2 O for an amount of time greater than or equal to 0.5 hours and less than or equal to 72 hours.
14 . The method of claim 13 , wherein the amount of time is inversely proportional to the Young's modulus of the non-structurally self-supporting material.
15 . The method of claim 1 , wherein exposing at least a portion of the structurally self-supporting material to H 2 O comprises exposing at least a portion of the structurally self-supporting material to H 2 O at a temperature greater than or equal to 25° C. and less than or equal to 150° C.
16 . The method of claim 15 , wherein the temperature is inversely proportional to the Young's modulus of the non-structurally self-supporting material.
17 . The method of claim 1 , wherein the structurally self-supporting material comprises a silyl-ether diacrylate polymer of the structure:
wherein:
R 1 and R 1 ′ are the same or different and are selected from the group consisting of —H, —CH 3 , C 1-10 alkyl, heteroalkyl, alkenyl, heteroalkenyl, alkynyl, heteroalkynyl, acyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, halo, hydroxyl, thiol, amino, carbonyl, and combinations thereof;
R 2 and R 2 ′ are the same or different and are selected from the group consisting of C 1-10 alkyl, heteroalkyl, alkenyl, heteroalkenyl, alkynyl, heteroalkynyl acyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, and combinations thereof;
R 3 and R 3 ′ are the same or different and are selected from the group consisting of —H, —CH 3 , C 1-10 alkyl, heteroalkyl, alkenyl, heteroalkenyl, alkynyl, heteroalkynyl, acyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, halo, hydroxyl, thiol, amino, carbonyl, and combinations thereof; and
n is greater than or equal to 2.
18 - 20 . (canceled)Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.