Decorative glow-in-the-dark concrete block
US-2024360047-A1 · Oct 31, 2024 · US
US10513656B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10513656-B2 |
| Application number | US-201515509801-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 8, 2015 |
| Priority date | Sep 8, 2014 |
| Publication date | Dec 24, 2019 |
| Grant date | Dec 24, 2019 |
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A pre-polymer formulation comprising quantum dots and a precursor for a polymer having a free volume parameter VFH2/γ with a value less than or equal to 0.03 cm3/g is disclosed. A pre-polymer formulation comprising quantum dots and a cyclohexylacrylate monomer is further disclosed. Also disclosed are a quantum dot composition including quantum dots dispersed in a polymer matrix, the quantum dot composition being prepared from a pre-polymer formulation comprising quantum dots and a precursor for a polymer having a free volume parameter VFH2/γ with a value less than or equal to cm3/g; a method; and other products including a quantum dot composition described herein.
Opening claim text (preview).
What is claimed is: 1. A pre-polymer formulation comprising: quantum dots; an adhesion promoter, wherein the adhesion promoter comprises a UV light curable optically transparent acrylic based material having adhesive properties; and a cyclohexylacrylate monomer. 2. A pre-polymer formulation in accordance with claim 1 wherein the UV light curable optically transparent acrylic based material a comprises bis[2-(methyloyloxy)ethyl]phosphate. 3. A pre-polymer formulation in accordance with claim 1 wherein the UV light curable optically transparent acrylic based material comprises a methacrylate monomer base structure including a phosphate functionality. 4. A pre-polymer formulation in accordance with claim 1 wherein the UV light curable optically transparent acrylic based material comprises an acrylate monomer base structure including a carboxylate functionality. 5. A pre-polymer formulation in accordance with claim 1 wherein the formulation includes the adhesion promoter in an amount greater than 0 up to about 10 weight percent of the formulation. 6. A pre-polymer formulation in accordance with claim 1 further comprising scatterers. 7. A pre-polymer formulation in accordance with claim 6 wherein the formulation includes the scatterers in an amount of 0.01 to about 15 weight percent of the formulation. 8. A pre-polymer formulation in accordance with claim 1 further comprising a thixotrope. 9. A pre-polymer formulation in accordance with claim 8 wherein the formulation includes the thixotrope in an amount greater than 0 up to about 15 weight percent of the formulation. 10. A pre-polymer formulation in accordance with claim 1 further comprising a photoinitiator. 11. A pre-polymer formulation in accordance with claim 10 wherein formulation includes the photoinitiator in an amount of about 0.01 to about 10 weight percent of the formulation. 12. A pre-polymer formulation in accordance with claim 1 wherein formulation includes quantum dots in an amount of about 0.01 to about 25 weight percent of the formulation. 13. A pre-polymer formulation in accordance with claim 1 further comprising an emission stabilizer. 14. A pre-polymer formulation in accordance with claim 13 wherein the emission stabilizer comprises at least one of potassium dodecyl phosphate and trioctyl phosphine oxide. 15. A pre-polymer formulation in accordance with claim 13 wherein the formulation includes the emission stabilizer in an amount greater than 0 up to about 10 weight percent of the formulation. 16. A pre-polymer formulation in accordance with claim 1 further including a cross-linking agent. 17. A pre-polymer formulation in accordance with claim 16 wherein the formulation includes the cross-linking agent in an amount of about 0.5 to about 15 weight percent of the formulation.
Use of particular materials as binders, particle coatings or suspension media therefor · CPC title
with zinc cadmium · CPC title
Nanooptics, e.g. quantum optics or photonic crystals · CPC title
Chemical synthesis, e.g. chemical bonding or breaking · CPC title
Group II-VI nonoxide compounds, e.g. CdxMnyTe · CPC title
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