Copolymer formulation for directed self-assembly, methods of manufacture thereof and articles comprising the same
US-2016251508-A1 · Sep 1, 2016 · US
US11274176B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11274176-B2 |
| Application number | US-201816490844-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 2, 2018 |
| Priority date | Mar 3, 2017 |
| Publication date | Mar 15, 2022 |
| Grant date | Mar 15, 2022 |
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A composite including a plurality of block copolymer chains dispersed in a base polymer, the block copolymer chains including a polymer block (A) and a polymer block (B) having lower affinity for the base polymer than that of the polymer block (A), wherein each of the block copolymer chains has the polymer block (A) at two or more locations of the block copolymer chain, and in at least some of the block copolymer chains, the polymer blocks (A) are at least partially located in the base polymer and the polymer blocks (B) are at least partially exposed from the base polymer.
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The invention claimed is: 1. A composite comprising a plurality of block copolymer chains dispersed in a base polymer, the block copolymer chains comprising a polymer block (A) and a polymer block (B) having lower affinity for the base polymer than that of the polymer block (A), wherein each of the block copolymer chains has the polymer block (A) at two or more locations of the block copolymer chain, and in at least some of the block copolymer chains, the polymer blocks (A) are at least partially located in the base polymer and the polymer blocks (B) are at least partially exposed from the base polymer. 2. The composite according to claim 1 , wherein the polymer block (B) constituting the block copolymer chains is incompatible with the base polymer. 3. The composite according to claim 1 , wherein the difference in SP value between the polymer block (A) and the polymer block (B) constituting the block copolymer chains is 1.5 (MPa) 1/2 or more. 4. The composite according to claim 3 , wherein the difference in SP value between the polymer block (A) constituting the block copolymer chains and the base polymer is 0.5 (MPa) 1/2 or less. 5. The composite according to claim 1 , wherein any glass transition temperature other than the glass transition temperature of the polymer block (A) itself and the glass transition temperature of the polymer block (B) itself is not observed for the block copolymer chains. 6. The composite according to claim 1 , wherein the polymer block (B) exposed from the base polymer is swollen by a good solvent for the polymer block (B). 7. A method for producing the composite according to claim 1 , comprising: mixing the base polymer and the block copolymer chains, so that in at least some of the block copolymer chains, the polymer blocks (A) are located in the base polymer and the polymer blocks (B) are exposed from the base polymer. 8. A method for producing the composite according to claim 1 comprising: mixing the base polymer and the block copolymer chains under heat to prepare a molten mixture; and cooling the molten mixture to cause a phase separation, so that in at least some of the block copolymer chains, the polymer blocks (A) are located in the base polymer and the polymer blocks (B) are exposed from the base polymer. 9. A method for producing the composite according to claim 1 , comprising: preparing a formed body comprising the block copolymer chains dispersed in the base polymer; and contacting a good solvent for the polymer block (B) with the surface of the formed body to cause a phase separation, so that in at least some of the block copolymer chains, the polymer blocks (A) are located in the base polymer and the polymer blocks (B) are exposed from the base polymer. 10. The method for producing the composite according to claim 7 , further comprising cross-linking the base polymer. 11. The method for producing the composite according to claim 10 , wherein the cross-linking of the base polymer is performed before, simultaneously with, or after the phase separation.
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