Polymer particle, polymer dispersion, method for producing said polymer dispersion, coating material produced from said polymer dispersion, and coated article
US-2015376390-A1 · Dec 31, 2015 · US
US9163096B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9163096-B2 |
| Application number | US-201214352984-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 3, 2012 |
| Priority date | Nov 24, 2011 |
| Publication date | Oct 20, 2015 |
| Grant date | Oct 20, 2015 |
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.
Disclosed is a method for producing a nitrile rubber comprising adding 0.1 to 5 parts by weight of at least one phosphate emulsifier selected from the group consisting of monoalkyl ether phosphate (MAP) represented by the following Formula 1 and dialkyl ether phosphate (DAP) represented by the following Formula 2, with respect to 100 parts by weight of monomers constituting the nitrile rubber. The method minimizes mold contamination during molding of produced nitrile rubber, eliminates the necessity of any process of removing mold contaminants, improves production efficiency and thus reduces defect rates of final molded articles.
Opening claim text (preview).
What is claimed is: 1. A method for producing a nitrile rubber comprising preparing a mixture comprising 0.1 to 5 parts by weight of at least one phosphate emulsifier selected from the group consisting of monoalkyl ether phosphate (MAP) represented by the following Formula 1 and dialkyl ether phosphate (DAP) represented by the following Formula 2 with respect to 100 parts by weight of monomers constituting the nitrile rubber and the monomers constituting the nitrile rubber; and producing the nitrile rubber by carrying out an emulsion polymerization of the monomers constituting the nitrile rubber wherein R represents an alkyl or alkylaryl group, M represents H, Na or K, and n is an integer. 2. The method according to claim 1 , wherein the monoalkyl ether phosphate is selected from the group consisting of the monoalkyl ether phosphate wherein R represents a C5-C20 alkyl or alkylaryl group, and n is integer of 2 to 10. 3. The method according to claim 1 , wherein the dialkyl ether phosphate is selected from the group consisting of the dialkyl ether phosphate wherein R represents a C5-C20 alkyl or alkylaryl group and n is an integer of 2 to 10. 4. The method according to claim 1 , wherein the monoalkyl ether phosphate and the dialkyl ether phosphate are used in a combination at a mix weight ratio of 1:99 to 99:1. 5. The method according to claim 1 , wherein the mixture further comprises an aliphatic organic acid or sulfonate emulsifier in an amount of 0.1 to 5 parts by weight with respect to 100 parts by weight of monomers constituting the nitrile rubber. 6. The method according to claim 5 , wherein the aliphatic organic acid comprises at least one selected from the group consisting of oleic acid, rosin acid, lauric acid, myristic acid, palmitic acid, stearic acid, and eicosanoic acid. 7. The method according to claim 5 , wherein the sulfonate emulsifier comprises at least one selected from the group consisting of sodium salts of naphthalene sulfonic acid, alkyl aryl sulfonate, alkali methyl alkyl sulfate, sulfonated alkylester, and alkali salts of rosin acid. 8. The method according to claim 1 , wherein the monomers constituting the nitrile rubber comprise a vinyl cyanide compound and a conjugated diene compound, and wherein the emulsion polymerization is configured to produce a nitrile rubber that is a random copolymer of the vinyl cyanide compound and the conjugated diene compound. 9. The method according to claim 8 , wherein the vinyl cyanide compound comprises at least one selected from the group consisting of acrylonitrile, methacrylonitrile, fumaronitrile, α-chloronitrile and α-cyanoethyl acrylonitrile, and is used in an amount of 10 to 60% by weight. 10. The method according to claim 8 , wherein the conjugated diene compound comprises at least one selected from the group consisting of 1,4-butadiene, 1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 2-ethyl-1,3-butadiene, 1,3-pentadiene and isoprene, and is used in an amount of 40 to 90% by weight. 11. The method according to claim 8 , wherein the vinyl cyanide compound comprises at least one selected from the group consisting of acrylonitrile, methacrylonitrile, fumaronitrile, α-chloronitrile and α-cyanoethyl acrylonitrile, and is used in an amount of 10 to 60% by weight, and wherein the conjugated diene compound comprises at least one selected from the group consisting of 1,4-butadiene, 1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 2-ethyl-1,3-butadiene, 1,3-pentadiene and isoprene, and is used in an amount of 40 to 90% by weight.
Related publications grouped by family.
Answers are generated from the same data shown on this page.