Wood article and process for the preparation of the wood article
US-12152130-B2 · Nov 26, 2024 · US
US9567476B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9567476-B2 |
| Application number | US-201313758803-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 4, 2013 |
| Priority date | Jan 17, 2008 |
| Publication date | Feb 14, 2017 |
| Grant date | Feb 14, 2017 |
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There is disclosed a process for obtaining a water-borne crosslinkable composition comprising a block copolymer comprising at least blocks [A] x [B] y (where x is an integer from 3 to 80 (inc.), where y is an integer ≧10 and where y>x) and a polymer P, the block copolymer-polymer having an acid value ≦150 mg KOH per g of block copolymer-polymer, where at least block [A] and [B] is obtained by a controlled radical polymerisation of at least one ethylenically unsaturated monomer via a reversible addition-fragmentation chain transfer (RAFT) mechanism in solution in the presence of a control agent and a source of free radicals; and where polymer P is obtained in the presence of blocks [A] x [B] y by an emulsion polymerisation process.
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The invention claimed is: 1. A process for obtaining a water borne non-biologically active crosslinkable block copolymer-polymer composition comprising a crosslinkable block copolymer comprising at least blocks [A] x [B] y , a polymer P, and a separate crosslinking agent, wherein the block copolymer-polymer composition has an acid value ≦150 mg KOH per g of block copolymer-polymer, wherein the process comprises: (a) subjecting at least one ethylenically unsaturated monomer by a controlled radical polymerization via a reversible addition-fragmentation chain transfer (RAFT) mechanism in solution in the presence of a control agent selected from the group consisting of dithioesters, thioethers-thiones, trithiocarbonates, dithiocarbamates, xanthates and mixtures thereof, and in the presence of a source of free radicals to obtain at least blocks [A] and [B], wherein a first block [A] is prepared followed by the polyemerisation of at least a second block [B] or wherein a first block [B] is prepared followed by the polymerization of at least a second block [A], thereby obtaining the block copolymer; wherein the wt % of blocks [A][B] together is in the range of from 0.5 to 50% based on the weight of the blocks [A][B] and the polymer P; and wherein block [A] comprises: i) 0 to 50 mol % of ethylenically unsaturated monomer units bearing crosslinking functional groups, wherein the ethylenically unsaturated monomer units bearing crosslinking functional groups are selected from the group consisting of acetoacetoxyethyl methacrylate, diacetone acrylamide, and mixtures thereof; ii) 50 to 100 mol % ethylenically unsaturated monomer units bearing water dispersing functional groups; iii) 0 to 50 mol % of ethylenically unsaturated monomers units selected from C1 18 alkyl(meth)acrylate monomers and styrenic monomers; iv) 0 to 35 mol % of ethylenically unsaturated monomers units different from those from i), ii) + iii); where i), ii), iii) + iv) add up to 100%; block [A] has a Hansch parameter <1.5; and block [A] has an average degree of polymerisation x, where x is an integer from 3 to 80; and wherein block [B] comprises: i) 5 to 80 mol % of ethylenically unsaturated monomer units bearing crosslinking functional groups, wherein the ethylenically unsaturated monomer units bearing crosslinking functional groups are selected from the group consisting of acetoacetoxyethyl methacrylate, diacetone acrylamide and mixtures thereof; ii) 0 to 20 mol % of ethylenically unsaturated monomer units bearing water dispersing functional groups; iii) 20 to 95 mol % of ethylenically unsaturated monomers units selected from C1 18 alkyl(meth)acrylate monomers and styrenic monomers; iv) 0 to 35 mol % of ethylenically unsaturated monomers units different from those from i), ii) + iii); where i), ii), iii) + iv) add up to 100%; block [B] has a Hansch parameter ≧1.5; and block [B] has an average degree of polymerisation y, where y is an integer ≧10, where y>x; (b) conducting an emulsion polymerization process in the presence of the block copolymer obtained according to step (a) to obtain the polymer P, wherein the polymer P comprises: i) 0 to 5 wt % of ethylenically unsaturated monomer units bearing crosslinking functional groups; ii) 0 to 5 wt % of ethylenically unsaturated monomer units bearing water dispersing functional groups; iii) 80 to 100 wt % of ethylenically unsaturated monomers units selected from C1 18 alkyl(meth)acrylate monomers and styrenic monomers; iv) 0 to 10 wt % of ethylenically unsaturated monomers units different from those from i), ii) + iii); where i), ii), iii) + iv) add up to 100%, and (c) combining the crosslinkable copolymer-polymer with a separate crosslinking agent to obtain the water-borne non-biologically active crosslinkable copolymer-polymer composition. 2. A process according to claim 1 where: block [A] comprises: (i) 0 to 20 mol % of ethylenically unsaturated monomer units bearing crosslinking functional groups, wherein the ethylenically unsaturated monomer units bearing crosslinking functional groups are selected from the group consisting of acetoacetoxyethyl methacrylate, diacetone acrylamide and hydroxyalkyl (meth)acrylates and mixtures thereof; iii) 0 to 50 mol % of ethylenically unsaturated monomers units selected from C1 12alkyl (meth)acrylate monomers and styrenic monomers; and iv) 0 to 20 mol %, of ethylenically unsaturated monomers units different from those from i), ii) + iii); block [B] comprises: iii) 20 to 95 mol % of ethylenically unsaturated monomers units selected from C1 12 alkyl(meth)acrylate monomers and styrenic monomers; and iv) 0 to 20 mol % of ethylenically unsaturated monomers units different from those from i), ii) + iii); and the polymer P comprises: iii) 80 to 100 wt % of ethylenically unsaturated monomers units selected C1 12alkyl(meth)acrylate monomers and styrenic monomers. 3. A process according to claim 1 , where the number average molecular weight of the block copolymer is in the range of from 1,000 to 50,000 g/mol. 4. A process according to claim 1 , where the weight average molecular weight of the polymer P is >50,000 g/mol. 5. A process according to claim 1 , any one of the wherein polymer P is more hydrophobic than block [A]. 6. A process according to claim 1 , where at least 20 wt % of polymer P is covalently bonded to the block copolymer. 7. A polymeric composition obtained by the process claimed in claim 1 . 8. A water borne composition comprising the block copolymer-polymer composition of claim 7 . 9. An ink, paint or adhesive comprising the block copolymer-polymer or a polymeric composition of claim 7 . 10. A coated substrate which comprises a coating formed of a formulation comprising the block copolymer-polymer composition of claim 7 .
Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers · CPC title
Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers · CPC title
Homopolymers or copolymers of acrylic acid esters · CPC title
using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title
Modified block copolymers · CPC title
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