Plant-based flexible material, process for preparation, and uses thereof
US-2024158638-A1 · May 16, 2024 · US
US2017130024A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017130024-A1 |
| Application number | US-201715415125-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 25, 2017 |
| Priority date | Aug 5, 2014 |
| Publication date | May 11, 2017 |
| Grant date | — |
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Polyhexahydrotriazine (PHT) and polyhemiaminal (PHA) materials form highly cross-linked polymers which can be used as binder resins in composite materials. A filler element functionalized with a primary amine group can be covalently bonded to the PHA/PHT polymer resins. Example filler elements include, without limitation, carbon nanotubes, silica materials, carbon and glass fibers, and nanoparticles. Filler materials are incorporated into polymeric materials to improve the mechanical strength or other characteristics of the polymeric material for various applications. Typical composite materials use thermosetting materials that, once set, are intractable. PHT and PHA materials can be reverted to starting materials by exposure to acids. Thus, composite components formed using these materials are recyclable.
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What is claimed is: 1 . A method of recycling a composite component, comprising: obtaining a composite component including: a polyhemiaminal (PHA) resin; and a filler element covalently bonded to the PHA resin; and exposing the composite component to an acid. 2 . The method of claim 1 , further comprising: recovering the filler element. 3 . The method of claim 1 , wherein the filler element is a nanoparticle. 4 . The method of claim 1 , wherein the filler element is a carbon fiber. 5 . The method of claim 1 , wherein the filler element is a glass fiber. 6 . The method of claim 1 , wherein the filler element is a single-wall nanotube. 7 . The method of claim 1 , wherein the filler element is a fullerene. 8 . The method of claim 1 , wherein the PHA resin comprises: a plurality of trivalent hemiaminal groups having the structure and a plurality of divalent bridging groups of formula: wherein L′ is a divalent linking group selected from the group consisting of —O—, —S—, —N(R′)—, —N(H)—, —R″—, and combinations thereof, wherein R′ comprises at least 1 carbon and R″ comprises at least one carbon, each starred bond of a given hemiaminal group is covalently linked to a respective one of the divalent bridging groups or the filler element, and each starred bond of a given bridging group is linked to a respective one of the trivalent hemiaminal groups. 9 . The method of claim 8 , wherein L′ is one of —O— or —S—. 10 . The method of claim 8 , wherein L′ is —N(R′)—, wherein R′ is selected from the group consisting of methyl, ethyl, propyl, isopropyl, phenyl, and combinations thereof. 11 . The method of claim 8 , wherein L′ is —CH 2 —. 12 . The method of claim 8 , wherein L′ is 9-fluorenylidenyl. 13 . The method of claim 8 , wherein the PHA resin includes a trivalent bridging group. 14 . The method of claim 8 , wherein the PHA resin includes at least one diluent group selected from the group consisting of and combinations thereof, wherein W′ is a monovalent radical selected from the group consisting of —H, —NH(R′), —N(R 2 )(R 3 ), —OH, —O(R 4 ), —S(R 5 ), —P(R 6 ), —R 7 , —CF 3 , and combinations thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 each comprise at least 1 carbon and each of R 1 -R 7 may be independent or the same, and the starred bond in each of the at least one diluents group is linked to a nitrogen of the PHA resin. 15 . A method of recycling a composite component, comprising: obtaining a composite component including: a polyhemiaminal (PHA) resin; and a carbon nanotube covalently bonded to the PHA resin; and exposing the composite component to an acid. 16 . The method of claim 15 , further comprising: recovering the carbon nanotube. 17 . The method of claim 15 , wherein the carbon nanotube is a single-walled nanotube. 18 . The method of claim 15 , wherein the PHA resin comprises: a plurality of trivalent hemiaminal groups having the structure and a plurality of divalent bridging groups of formula: wherein L′ is a divalent linking group selected from the group consisting of —O—, —S—, —N(R′)—, —N(H)—, —R″—, and combinations thereof, wherein R′ comprises at least 1 carbon and R″ comprises at least one carbon, each starred bond of a given hemiaminal group is covalently linked to a respective one of the divalent bridging groups or the filler element, and each starred bond of a given bridging group is linked to a respective one of the trivalent hemiaminal groups.
Recycling of unreacted starting or intermediate materials · CPC title
Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors · CPC title
Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors · CPC title
with at least three nitrogen atoms in the ring · CPC title
Chemically modified polycondensates · CPC title
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