Binder-consolidated textile fabric, method for its manufacture and its use
US-12559884-B2 · Feb 24, 2026 · US
US12018430B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12018430-B2 |
| Application number | US-202117349802-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 16, 2021 |
| Priority date | Dec 18, 2018 |
| Publication date | Jun 25, 2024 |
| Grant date | Jun 25, 2024 |
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 flame-retardant ultraviolet-resistant aramid fiber, the preparation method therefor comprising the following steps: adding nanoparticles into a hydrogen peroxide solution, performing magnetic stirring for 0.5-1 h, adding a sulfuric acid solution, and further performing magnetic stirring for 0.5 h; performing filtering to obtain a filter cake, and washing the filter cake with water and drying same to obtain modified particles; modifying the modified particles with curcumin and dopamine to obtain organic substance-modified particles; and finally subjecting the organic substance-modified particles to a reaction with a silicon methoxylated aramid fiber, so as to obtain a surface-modified aramid fiber. The present invention has high ultraviolet absorption and extremely low catalytic activity, avoiding damage to a fiber structure by photocatalysis in a radiation process, and in particular improving flame retardancy of the aramid fiber.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a flame-retardant ultraviolet-resistant aramid fiber, comprising the following steps: (1) dissolving a cerium salt and an inorganic base in water, stirring for 20 to 45 min, adding hydrogen peroxide to obtain a suspension, adjusting the pH of the suspension to 10 to 14, reacting at 20 to 25° C. for 10 to 20 h, washing and filtering, drying, calcining at 500 to 800° C. for 1 to 3 h to obtain a nano-cerium oxide; dispersing the nano-cerium oxide, a boron source and a nitrogen-containing compound in a mixed solution of ethanol and water, ultrasonic agitating for 0.5 to 1.5 h, steaming and drying, then dispersing in an aqueous solution of cobalt nitrate, ultrasonic agitating for 0.5 to 1 h, then steaming and drying to obtain a solid substance; calcining the solid substance at 850 to 950° C. for 13 to 15 h under a nitrogen source gas, and then crushing to obtain nanoparticles; (2) adding the nanoparticles into a hydrogen peroxide solution, magnetic stirring for 0.5 to 1 h, then adding sulfuric acid solution, and continuing to magnetic stir for 0.5 h; then filtering to obtain a filter cake, and then washing the filter cake and drying to obtain modified particles; (3) adding the modified particles and dopamine hydrochloride to a buffer having a pH of 8.3 to 8.8; and stirring at room temperature for 2 to 3 hours; then adding a curcumin ethanol solution and continuing to stir for 1-2 h; and then filtering, washing and drying to obtain organic modified particles; (4) immersing a silicon methoxylated aramid fiber in an aqueous solution of trimethylsilanol, and shaking for 0.5 to 1 h; and then immersing in an aqueous solution of the organic modified particles, then shaking at 70° C.-80° C. for 2-3 h; after that, washing and drying to obtain the flame-retardant ultraviolet-resistant aramid fiber. 2. The method according to claim 1 , wherein the aramid fiber is a para-aramid fiber or a meta-aramid fiber. 3. The method according to claim 1 , wherein the inorganic base is an alkali metal hydroxide selected from sodium hydroxide, potassium hydroxide or a combination thereof; the cesium salt is cerium nitrate, cerium chloride, or a combination; boron source is boric acid or metaboric acid; the nitrogen-containing compound is urea, melamine, or ammonium bromide. 4. The method according to claim 1 , wherein a mass ratio of the nano-cerium oxide, the boron source, the nitrogen-containing compound, cobalt nitrate is 100:(30 to 50):(60 to 120):(10 to 13). 5. The method according to claim 1 , wherein the buffer is one of Tris-HCl or disodium hydrogen phosphate-sodium dihydrogen phosphate buffer. 6. The method according to claim 1 , wherein a mass ratio of the nanoparticles, hydrogen peroxide solution, and sulfuric acid solution is 100:(60 to 70):(5 to 7). 7. The method according to claim 1 , wherein a mass ratio of the modified particles, dopamine hydrochloride, curcumin is 100:(30 to 50):(8 to 12). 8. The method according to claim 1 , wherein a mass ratio of the silicon methoxylated aramid fiber, the organic modified particles and trimethylsilanol is 1:(2 to 9):(0.3 to 0.35). 9. The method according to claim 1 , wherein a mass ratio of the cerium salt and the inorganic base is 100:(20 to 50). 10. The method according to claim 1 , wherein the nitrogen source gas is nitrogen or ammonia.
Flame or heat resistance, fire retardancy properties · CPC title
Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments · CPC title
Aromatic polyamides · CPC title
combined with mechanical treatment · CPC title
with at least one carbon-silicon bond · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.