Moisture curable compositions
US-2024400829-A1 · Dec 5, 2024 · US
US2026008927A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2026008927-A1 |
| Application number | US-202519243216-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 19, 2025 |
| Priority date | Jul 8, 2024 |
| Publication date | Jan 8, 2026 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A self-diagnosis and self-repair intelligent coating based on microfluidic technology and a preparation method thereof are provided. Microcapsules are prepared by combining microfluidic T-junction and interfacial polymerization. The wall material of the microcapsules is made of polyurea, and the core material is made of diagnostic agent, repair agent and photoinitiator. Self-diagnosis and self-repair microcapsules are evenly distributed in the coating with silicone resin as matrix.
Opening claim text (preview).
1 . A self-diagnosis and self-repair intelligent coating based on microfluidic technology, wherein the coating is made from a composition comprising microcapsules and a resin matrix; the microcapsules consist of a shell material and coating materials; the shell material is polyurea; the coating materials are a repair agent, a diagnostic agent and a photoinitiator; the repair agent is 1,3-bis(3-glycidyl propyl)-1,1,3,3-tetramethyldisiloxane; the diagnostic agent is rhodamine B; the photoinitiator is triarylsulfonium hexafluorophosphate; and the resin matrix is a mixture of self-drying silicone resin and silane coupling agent with a mass ratio of 20:1; and a mass content of the microcapsules in the composition is 11.1-14.3%. 2 .- 6 . (canceled) 7 . A preparation method of the self-diagnosis and self-repair intelligent coating based on the microfluidic technology according to claim 1 , the preparation method comprising: using the microfluidic technology, pumping a dispersed phase solution and a continuous phase solution into polytetrafluoroethylene tube 1 and polytetrafluoroethylene tube 2 in a microfluidic chip respectively; in the chip, cutting the dispersed phase solution into uniform droplets with the continuous phase solution, and introducing the droplets into a reaction solution with continuous mechanical stirring to form a polyurea film, and after the chip cutting the droplets is finished, placing the reaction solution in a water bath pot and continuously heating and stirring, wherein the polyurea film grows thicker and becomes polyurea-based microcapsules; and washing the obtained polyurea-based microcapsules with cyclohexane, sonicating, centrifuging, and then naturally drying to obtain the microcapsules; mixing the microcapsules with the resin matrix to obtain a self-diagnosis and self-repair intelligent coating material based on the microfluidic technology; and coating the self-diagnosis and self-repair intelligent coating material based on the microfluidic technology on a glass slide and curing to obtain the self-diagnosis and self-repair intelligent coating based on the microfluidic technology, wherein a method for preparing the dispersed phase solution comprises: ultrasonically mixing the 1,3-bis(3-glycidyl propyl)-1,1,3,3-tetramethyldisiloxane, the triarylsulfonium hexafluorophosphate, the rhodamine B and tetraethylenepentamine, wherein a method for preparing the continuous phase solution comprises: ultrasonically mixing an n-hexadecane solution and polyethylene glycol dimeric hydroxy stearate, wherein a method for preparing the reaction solution comprises: ultrasonically mixing 4,4-dicyclohexylmethane diisocyanate, decalin, polyethylene glycol dimeric hydroxy stearate and triethylenediamine. 8 . The preparation method according to claim 7 , wherein a mass ratio of the 1,3-bis(3-glycidyl propyl)-1,1,3,3-tetramethyldisiloxane, the triarylsulfonium hexafluorophosphate, the rhodamine B and the tetraethylenepentamine is 1.1:0.09:0.09:1. 9 . The preparation method according to claim 7 , wherein a mass ratio of the n-hexadecane solution to the polyethylene glycol dimeric hydroxy stearate in the method for preparing the continuous phase solution is 2.784:0.027. 10 . The preparation method according to claim 7 , wherein a mass ratio of the 4,4-dicyclohexylmethane diisocyanate, the decalin, the polyethylene glycol dimeric hydroxy stearate and the triethylenediamine in the method for preparing the reaction solution is 9:67.2:0.75:0.75. 11 . The preparation method according to claim 7 , wherein a flow rate of the dispersed phase solution is 0.02 mL/min, and a flow rate of the continuous phase solution is 0.4-0.6 mL/min. 12 . The preparation method according to claim 7 , wherein a speed of the mechanical stirring is 100 rpm; and parameters of the heating and stirring are: a temperature of 40-60° C., a duration of 1-2 h, and a stirring speed of 200 rpm.
Polysiloxanes · CPC title
Interfacial polymerisation · CPC title
organic · CPC title
macromolecular (C09D7/41-C09D7/48 take precedence) · CPC title
characterised by shape, e.g. fibres, flakes or microspheres · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.