Crosslinked Polymer Compositions, Gas Separation Membranes of Such Crosslinked Polymer Compositions, Methods Of Making Such Membranes, and Methods of Separating Gases Using Such Membranes
US-2015122121-A1 · May 7, 2015 · US
US10633554B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10633554-B2 |
| Application number | US-201716323452-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 11, 2017 |
| Priority date | Dec 19, 2016 |
| Publication date | Apr 28, 2020 |
| Grant date | Apr 28, 2020 |
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The present invention provides a surface modification method based on the polymerization and cross-linking solidification of dopamine and/or its derivatives, which belongs to the technical field about composite material fabrication. The principle of dopamine polymerization and the formation process of polydopamine coating layer are the foundation of the present invention. This innovative method is established after deeply analyzing the failure mechanism of polydopamine coating layer in severe environments, such as organic solvents and acidic/alkalic environments. The critical work is finding out an eligible cross-linking agent which could react with the active functional groups in polydopamine. After cross-linking reaction, the soluble low-molecular-weight dopamine oligomers could be transformed into the insoluble three-dimensional stereographic networks. In this instance, the interaction between polydopamine molecules, and the adhesion between polydopamine coating layer and substrate materials, can be significantly strengthened. After the cross-linking solidification, the hydrophilic polydopamine coating layer could be stable and effective for long-term utilization in severe environments, e.g., organic solvents and acidic/alkalic environments, and thereby expand the application scope of the surface modification method based on dopamine polymerization greatly.
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We claim: 1. A surface modification method based on the polymerization and cross-linking solidification of dopamine and/or its derivatives, comprising the following steps: 1) Preparation of polydopamine coating layer for modification: immersing the to-be-modified substrates into the solution containing dopamine and/or its derivatives, or coating the solution containing dopamine or its derivatives onto the to-be-modified substrates for surface modification; and conducting oxidative auto-polymerization for dopamine or its derivatives at 30-70° C., wherein the reaction time is determined by the coating degree required for surface modification; 2) Cross-linking solidification of the polydopamine coating layer for modification: after surface modification with polydopamine through step (1), washing the substrates to remove unpolymerized dopamine and/or its derivatives remaining on the surface; immersing the modified substrates into the cross-linking solution, or coating the cross-linking solution onto the modified substrates for solidification; and reacting at 30-90° C. for 3-6 h to complete cross-linking solidification of the coating layer of polymerized dopamine and/or its derivatives, to enhance the long-term stability of the coating layer for surface modification in organic solvents and acidic/alkalic environments. 2. The surface modification method according to claim 1 , wherein the dopamine derivatives are one or a mixture of more than two of 3,4-dihydroxypheny-lalanine, 3,4-dihydroxypheny-methacrylamide, hydroquinone and 1,2-benzenediol. 3. The surface modification method according to claim 1 , wherein the cross-linking agent is one or a mixture of more than two of paraformaldehyde, formaldehyde, acetaldehyde, glutaraldehyde, polyamine and epoxy olefins. 4. The surface modification method according to claim 1 , wherein the solution for surface modification contains one or a mixture of more than two of dopamine, and its derivatives; and the surface modification solution could be an alkaline system, a neutral medium or an acid system. 5. The surface modification method according to claim 3 , wherein the surface modification solution contains one or a mixture of more than two of dopamine, and its derivatives; and the surface modification solution is an alkaline system, a neutral medium or an acid system. 6. The surface modification method according to claim 1 , wherein the substrate materials can be inorganic materials, organic materials or metallic materials, and the morphologies of substrate materials could be particles, fibers, sticks, plates, networks or porous membranes. 7. The surface modification method according to claim 3 , wherein the substrate materials could be inorganic materials, organic materials or metallic materials, and the morphologies of substrate materials could be particles, fibers, sticks, plates, networks or porous membranes. 8. The surface modification method according to claim 4 , wherein the substrate materials could be inorganic materials, organic materials or metallic materials, and the morphologies of substrate materials could be particles, fibers, sticks, plates, networks or porous membranes. 9. The surface modification method according to claim 6 , wherein the inorganic materials could be silica, graphite, carbon materials, ceramic materials or metallic oxide; and the organic materials could be polymers or bio-macromolecules. 10. The surface modification method according to claim 7 , wherein the inorganic materials could be silica, graphite, carbon materials, ceramic materials or metallic oxide; and the organic materials could be polymers or bio-macromolecules.
with only one layer of a composition containing a polymer binder (with more layers C08J7/042) · CPC title
containing one or more nitrogen atoms as the only heteroatom, e.g. carbazole · CPC title
Polyamines · CPC title
Copolymers · CPC title
Homopolymers · CPC title
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