Process for making crosslinked cable insulation using high melt strength ethylene-based polymer made in a tubular reactor and optionally modified with a branching agent
US-11912852-B2 · Feb 27, 2024 · US
US9527942B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9527942-B2 |
| Application number | US-201314376683-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 5, 2013 |
| Priority date | Feb 10, 2012 |
| Publication date | Dec 27, 2016 |
| Grant date | Dec 27, 2016 |
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Polymer latex binders useful for preparing coating compositions containing low levels of, or which are substantially free of, volatile organic compounds (VOCs) such as volatile freeze-thaw additives are prepared by multistage emulsion polymerization, wherein one stage provides a copolymer having a relatively high glass transition temperature and containing an oxyalkylene-containing (meth)acrylate comonomer.
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What is claimed is: 1. A multiphase emulsion polymer for coating compositions, said multiphase emulsion polymer comprising at least one hard phase polymer having a glass transition temperature of from 0 to 100° C. and at least one soft phase polymer having a glass transition temperature of less than 0° C. and at least 20 to 100° C. lower than the glass transition temperature of the hard phase polymer, wherein the hard phase polymer is a copolymer of one or more ethylenically unsaturated monomer, and one or more oxyalkylene-containing (meth)acrylate corresponding to formula (I) or (II) or a mixture thereof: CH 2 ═C(R 1 )—C(═O)—O—[X—O] n —R 2 ; (I) CH 2 ═C(R 1 )—C(═O)—O—[X—O] n —P(═O)(OY) 2 ; (II) wherein R 1 is or CH 3 , R 2 is H or a C 1 -C 8 alkyl group, each X is independently —(CH 2 ) 2 —, —CH 2 CH(CH 3 )— or —CH(CH 3 )CH 2 —, each Y is independently H, ammonium or an alkali metal atom, and n is an integer of from 1 to 30, wherein the soft phase polymer is a copolymer of monomers selected from the group consisting of C1-C18 alkyl(meth)acrylates, halo- and hydroxyl substituted alkyl esters of (meth)acrylic acid, vinyl esters of linear and branched caboxylic acids, having 2 to 20 carbon atoms, unsaturated C3-C6 monocarboxylic acid, monoesters of unsaturated C4-C6 dicarboxylic acids, unsaturated C4-C6 dicarboxylic acids, (meth)acrylonitrile, cycloalkyl(meth)acrylates, aryl and alkaryl esters of (meth)acrylates, acetoacetate-containing acrylate monomers, olefins, dienes, wherein the at least one hard polymer phase is formed as a first stage polymer and the at least one soft polymer phase is subsequently polymerized in the presence of the first stage polymer, and wherein the multiphase emulsion polymer is in the form of latex particles and wherein the latex particles comprise an inner phase comprised of the soft phase polymer and an outer phase comprised of the hard phase polymer. 2. The multiphase emulsion polymer of claim 1 , wherein the at least one ethylenically unsaturated monomer is a mixture of at least one alkyl (meth)acrylate, methacrylic acid and at least one wet adhesion monomer. 3. The multiphase emulsion polymer of claim 1 , wherein the at least one ethylenically unsaturated monomer is a mixture of butyl acrylate, methyl methacrylate, methacrylic acid and hydroxyethyl ethylene urea methacrylate. 4. The multiphase emulsion polymer of claim 1 , wherein the hard phase polymer is a copolymer comprised of 0.5 to 10% by weight of oxyalkylene-containing (meth)acrylate. 5. The multiphase emulsion polymer of claim 1 , wherein the oxyalkylene-containing (meth)acrylate is a polyethylene glycol methacrylate. 6. The multiphase emulsion polymer of claim 1 , wherein the oxyalkylene-containing (meth)acrylate is a phosphate ester of a polyethylene glycol methacrylate. 7. The multiphase emulsion polymer of claim 1 , wherein the multiphase emulsion polymer is in the form of latex particles having an average particle size of less than 350 nm. 8. The multiphase emulsion polymer of claim 1 , wherein the soft phase polymer is a copolymer of C1-C18 alkyl (meth)acrylates. 9. The multiphase emulsion polymer of claim 1 , wherein the soft phase polymer is a copolymer of butyl acrylate and methyl methacrylate. 10. The multiphase emulsion polymer of claim 1 , wherein the soft polymer phase represents from 90% to 40% by weight of the multiphase emulsion polymer and the hard polymer phase represents from 10% to 60% by weight of the multiphase emulsion polymer, the total weight amount of soft polymer phase and hard polymer phase equaling 100%. 11. A method of making a polymer latex binder for coating compositions, comprising: (a) copolymerizing an aqueous multiphase emulsion of one or more ethylenically unsaturated monomer, and one or more oxyalkylene-containing (meth)acrylate corresponding to formula (I) or (II) or a mixture thereof: CH 2 ═C(R 1 )—C(═O)—O—[X—O] n —R 2 ; (I) CH 2 ═C(R 1 )—C(═O)—O—[X—O] n —P(═O)(OY) 2 ; (II) wherein R 1 is or CH 3 , R 2 is H or a C 1 -C 8 alkyl group, each X is independently —(CH 2 ) 2 —, —CH 2 CH(CH 3 )— or —CH(CH 3 )CH 2 —, each Y is independently H, ammonium or an alkali metal atom, and n is an integer of from 1 to 30, to form a hard phase polymer having a glass transition temperature from 0 to 100° C.; (b) polymerizing one or more additional monomers in the presence of the hard phase polymer to form a soft phase polymer; wherein the soft phase polymer is a copolymer of monomers selected from the group consisting of C1-C18 alkyl(meth)acrylates, halo- and hydroxyl substituted alkyl esters of (meth)acrylic acid, vinyl esters of linear and branched caboxylic acids, having 2 to 20 carbon atoms, unsaturated C3-C6 monocarboxylic acid, monoesters of unsaturated C4-C6 dicarboxylic acids, unsaturated C4-C6 dicarboxylic acids, (meth)acrylonitrile, cycloalkyl(meth)acrylates, aryl and alkaryl esters of (meth)acrylates, acetoacetate-containing acrylate monomers, olefins, dienes, wherein the hard phase polymer has a glass transition temperature of from 0 to 100° C. and the soft phase polymer has a glass transition temperature of less than 0° C. and at least 20 to 100° C. lower than the glass transition temperature of the hard phase polymer; wherein the emulsion polymer is in the form of latex particles, and wherein the latex particles comprise an outer phase comprised of the hard polymer phase and an inner phase comprised of the soft polymer phase. 12. The method of claim 11 , wherein the at least one ethylenically unsaturated monomer is a mixture of at least one alkyl (meth)acrylate, methacrylic acid and at least one wet adhesion monomer. 13. The method of claim 11 , wherein the at least one ethylenically unsaturated monomer is a mixture of butyl acrylate, methyl methacrylate, methacrylic acid and hydroxyethyl ethylene urea methacrylate. 14. The method of claim 11 , wherein the hard phase polymer is a copolymer comprised of 0.5 to 10% by weight of oxyalkylene-containing (meth)acrylate. 15. The method of claim 11 , wherein the oxyalkylene-containing (meth)acrylate is a polyethylene glycol methacrylate. 16. The method of claim 11 , wherein the oxyalkylene-containing (meth)acrylate is a phosphate ester of a polyethylene glycol methacrylate. 17. The method of claim 11 , wherein the multiphase emulsion polymer is in the form of latex particles having an average particle size of less than 350 nm. 18. The method of claim 11 , wherein the soft phase polymer is a copolymer of C1-C18 alkyl (meth)acrylates. 19. The method of claim 11 , wherein the soft phase polymer is a copolymer of butyl acrylate and methyl methacrylate. 20. The method of claim 11 , wherein the soft polymer phase represents from 90% to 40% by weight of the multiphase emulsion polymer and the hard polymer phase represents from 10% to 60% by weight of the multiphase emulsion polymer, the total weight amount of soft polymer phase and hard polymer phase equaling 100%.
grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
on to unsaturated polyethers, polyoxymethylenes or polyacetals · CPC title
anionic · CPC title
grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds (C09D151/04, C09D151/06 take precedence) · CPC title
Methyl esters {, e.g. methyl (meth)acrylate} · CPC title
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