Living radical polymer, composition, resin-coated pigment, and method for producing living radical polymer
US-2024101742-A1 · Mar 28, 2024 · US
US9487651B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9487651-B2 |
| Application number | US-201214391008-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 10, 2012 |
| Priority date | Aug 17, 2011 |
| Publication date | Nov 8, 2016 |
| Grant date | Nov 8, 2016 |
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The present invention relates to a hemispherical polymethylmethacrylate bead, wherein the hemispherical polymethylmethacrylate bead of the invention has high adhesive property and oil absorption when applied to cosmetics, medical supply, household items, display devices, lighting fixtures, and miscellaneous goods and especially, it enables cheerful color when applied to cosmetics in comparison with spherical polymethylmethacrylate beads.
Opening claim text (preview).
What is claimed is: 1. A polymethylmethacrylate bead wherein the shape of the polymethylmethacrylate bead is hemispherical and the polymethylmethacrylate bead has oil absorption of 2.4 to 3.0 cc/g. 2. The polymethylmethacrylate bead as claimed in claim 1 , wherein the hemispherical polymethylmethacrylate bead has a TAP density of 0.1 to 0.5 g/ml. 3. A method for preparing a hemispherical polymethylmethacrylate bead comprising adding an acrylic monomer, a crosslinking agent, an initiator, and a cosolvent to a solvent to polymerize them, and then washing and drying them, wherein the difference between the boiling point (BP) of the cosolvent and the reaction temperature of the initiator is −5 to 15° C., wherein the cosolvent is at least one selected from the group consisting of cyclohexane, ethyl acetate, methyl ethyl ketone, ortho chloro toluene, and isopropyl alcohol, and it is included in an amount of 100 to 400 parts by weight with regard to the total 100 parts by weight of the monomers to be used for the preparation of the bead. 4. The method for preparing the hemispherical polymethylmethacrylate bead as claimed in claim 3 , wherein the difference between the boiling point (BP) of the cosolvent and the reaction temperature of the initiator is 0 to 10° C. 5. The method for preparing the hemispherical polymethylmethacrylate bead as claimed in claim 3 , wherein at least one stabilizer selected from the group consisting of polyvinyl pyrrolidone, polyvinyl methyl ether, polyethyleneimine, poly acrylic acid, polyvinyl alcohol, vinyl acetate copolymer, ethyl cellulose and hydroxypropyl cellulose was used in an amount of 0.1 to 5 parts by weight with regard to the total 100 parts by weight of the monomers to be used for the preparation of the bead. 6. The method for preparing the hemispherical polymethylmethacrylate bead as claimed in claim 3 , wherein the initiator is at least one selected from the group consisting of 2,2-azobisisobutyronitrile, 4,4-azobis(4)-cyanopentanoic acid, 2,2-azobis(2-methylbutyronitrile), 2,2-azobis(2,4-dimethylvalenonitrile), benzoyl peroxide, lauryl peroxide, octanoyl peroxide, and 3,3,5-trimethyl hexanoyl peroxide, and it is included in an amount of 0.1 to 5 parts by weight with regard to the total 100 parts by weight of the monomers to be used for the preparation of the bead. 7. The method for preparing the hemispherical polymethylmethacrylate bead as claimed in claim 3 , further comprising a sorting process after the drying step. 8. A cosmetic, medical supply, household item, display device or lighting fixture comprising the hemispherical polymethylmethacrylate described in claim 1 .
Methyl esters {, e.g. methyl (meth)acrylate} · CPC title
Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids · CPC title
Homopolymers or copolymers of methyl methacrylate · CPC title
Particulate matter [e.g., sphere, flake, etc.] · CPC title
Homopolymers or copolymers of methyl methacrylate · CPC title
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