Thermally printable paper article with elastic interspersing layer
US-2017334229-A1 · Nov 23, 2017 · US
US10414938B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10414938-B2 |
| Application number | US-201515303415-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 7, 2015 |
| Priority date | Apr 11, 2014 |
| Publication date | Sep 17, 2019 |
| Grant date | Sep 17, 2019 |
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The invention relates to a process for preparing an aqueous dispersion of a polymer P, which comprises the emulsion polymerization of vinyl acetate, an acrylate monomer, which is a C 1 -C 10 alkyl acrylate or a C 1 -C 10 methacrylate, an α,β-ethylenically unsaturated C 3 -C 8 carboxylic acid, glycidyl methacrylate or glycidyl acrylate, optionally an ethylenically unsaturated sulfonic acid and optionally an ethylenically unsaturated other monomer. Furthermore, the aqueous polymer dispersion obtainable from this process and a powder form thereof are disclosed. They are useful for a paper coating slip containing one of the aforementioned forms. A paper or a cardboard, which is coated with the paper coating slip, shows surface strength, which is expressed by a good dry pick resistance, a good wet pick resistance or good offset test results. The aqueous polymer dispersion or the powder form thereof is furthermore useful as a binder.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing an aqueous dispersion of a polymer P, the process comprising: emulsifying monomers consisting of (a), (b), (c), (d), (e) and optionally (f) in an aqueous medium: (a) vinyl acetate, (b) at least one acrylate monomer, which is a C 1 -C 10 alkyl acrylate or a C 1 -C 10 alkyl methacrylate, (c) at least one α,β-ethylenically unsaturated C 3 -C 6 carboxylic acid, (d) glycidyl methacrylate or glycidyl acrylate, (e) at least one ethylenically unsaturated sulfonic acid, and (f) at least one ethylenically unsaturated monomer, which is different from the monomers (a), (b), (c), (d) or (e), and is selected from the group consisting of a cycloalkene, a conjugated aliphatic C 4 -C 9 diene, an ester of vinyl alcohol and a C 2 -C 15 monocarboxylic acid, a C 5 -C 10 cycloalkyl acrylate, a C 5 -C 10 cycloalkyl methacrylate, di(C 1 -C 10 alkyl) maleinate, di(C 1 -C 10 alkyl) fumarate, a vinylaromatic compound, an ethylenically unsaturated C 3 -C 8 -monocarbonitrile, an ethylenically unsaturated C 4 -C 8 -dicarbonitrile, an ethylenically unsaturated C 3 -C 8 monocarboxamide, an ethylenically unsaturated C 4 -C 8 dicarboxamide, ureido methacrylate, ureido acrylate, allyl methacrylate or allyl acrylate, and polymerizing the monomers in the presence of a free-radical initiator, wherein the content of vinyl acetate is from 70 to 94.7 parts by weight of the monomers, the content of the at least one acrylate monomer is from 5 to 25 parts by weight of the monomers, the content of the at least one a,b-ethylenically unsaturated C 3 -C 6 carboxylic acid is from 0.1 to 10 parts by weight of the monomers, the content of glycidyl methacrylate or glycidyl acrylate is from 0.1 to 10 parts by weight of the monomers, the content of the at least one ethylenically unsaturated sulfonic acid is from 0.1 to 5 parts by weight of the monomers, the content of the optional at least one other ethylenically unsaturated monomer when present, is from 0.1 to 15 parts by weight of the monomers, and the sum total of the parts by weight of the monomers (a), (b), (c), (d), (e) and (f) is 100. 2. The process according to claim 1 , wherein the content of vinyl acetate is from 70 to 85 parts by weight of the monomers. 3. The process according to claim 1 , wherein (b) the at least one acrylate monomer is n-butyl acrylate or ethylhexyl acrylate, and (c) the at least one α,β-ethylenically unsaturated C 3 -C 6 carboxylic acid is acrylic acid, methacrylic acid, crotonic acid, fumaric acid, maleic acid, maleic acid anhydride, 2-methyl maleic acid, 2-methyl maleic acid anhydride or itaconic acid. 4. The process according to claim 1 , wherein (e) the at least one ethylenically unsaturated sulfonic acid is vinyl sulfonic acid or 2-acrylamido-2-methylpropane sulfonic acid. 5. The process according to claim 1 , wherein (b) the at least one acrylate monomer is n-butyl acrylate, (c) the at least one α,β-ethylenically unsaturated C 3 -C 6 carboxylic acid is acrylic acid or methacrylic acid, and (e) the at least one ethylenically unsaturated sulfonic acid is vinylsulfonic acid. 6. The process according to claim 1 , wherein the content of vinyl acetate is from 75 to 85 parts by weight of the monomers, the content of the at least one acrylate monomer is from 7 to 19 parts by weight of the monomers, the content of the at least one α,β-ethylenically unsaturated C 3 -C 6 carboxylic acid is from 0.5 to 5 parts by weight of the monomers, the content of glycidyl methacrylate or glycidyl acrylate is from 0.5 to 8 parts by weight of the monomers, the content of the at least one ethylenically unsaturated sulfonic acid is from 0.1 to 2 parts by weight of the monomers, the content of the at least one other ethylenically unsaturated monomer when optionally present is from 0.1 to 10 parts by weight of the monomers, and the sum total of the parts by weight of the monomers (a), (b), (c), (d), (e) and (f) is 100. 7. The process according to claim 1 , wherein the monomers (a), (b), (c), (d), (e) and optionally (f) are chosen in a way such that the polymer P, which is obtained after removal of water from the aqueous dispersion, possesses a glass transition temperature in the range from 20° C. to 40° C. as determined by the norm ISO 11357-2.
Polyalkenylalcohols; Polyalkenylethers; Polyalkenylesters · CPC title
Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof · CPC title
Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates · CPC title
Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters · CPC title
inorganic · CPC title
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