Additive for suspensions
US-10106460-B2 · Oct 23, 2018 · US
US10988415B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10988415-B2 |
| Application number | US-201615762521-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 22, 2016 |
| Priority date | Sep 24, 2015 |
| Publication date | Apr 27, 2021 |
| Grant date | Apr 27, 2021 |
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The present invention relates to the use of a copolymer as a dispersant for binder compositions based on calcium sulfate, the copolymer having a polymer backbone and sidechains bound thereto, and at least one ionizable monomeric unit M1 and at least one sidechain-carrying monomeric unit M2, characterized in that the copolymer has, in a direction along the polymer backbone, a non-random distribution of the monomeric units M1 and/or of the monomeric units M2.
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The invention claimed is: 1. A method comprising introducing a copolymer as a dispersant into a binder composition that includes at least one mineral binder, the binder composition being based on calcium sulfate, wherein the copolymer comprises a polymer backbone and side chains bonded thereto and there are at least one ionizable monomer unit M1 and at least one side chain-bearing monomer unit M2, the copolymer has a nonrandom distribution of the monomer units Ml and/or the monomer units M2 in a direction along the polymer backbone in that the copolymer has a gradient structure in at least one section AA in a direction along the polymer backbone with respect to the ionizable monomer unit M1 and/or with respect to the side chain-bearing monomer unit M2, and the copolymer, in addition to the at least one section AA having a gradient structure, has a further section AB, wherein there is essentially a constant local concentration of the monomers and/or a statistical or random distribution of the monomers over the entire section AB, a proportion of the calcium sulfate, based on all the mineral binder in the binder composition, is at least 30% by weight, a molar ratio of the monomer units Ml to the monomer units M2 in the copolymer is in the range of 0.5-6, the ionizable monomer unit M1 in the copolymer has a structure of the formula I the side chain-bearing monomer unit M2 includes a structure of the formula II where R 1 forms a ring together with R 4 to give —CO—O—CO—, or R 1 , in each case independently, is —COOM and/or —SO 2 -0M, and R 4 , in each case independently, is H, —COOM or an alkyl group having 1 to 5 carbon atoms; M, independently of one another, represents H + , an alkali metal ion, an alkaline earth metal ion, a di- or trivalent metal ion, an ammonium ion or an organic ammonium group; R 2 , R 3 , R 5 and R 6 , in each case independently, are H or an alkyl group having 1 to 5 carbon atoms; R 7 , in each case independently, is H, —COOM or an alkyl group having 1 to 5 carbon atoms; m=0, 1 or 2; p=0 or 1; X, in each case independently, is —O— or —NH—; R 8 is a group of the formula -[AO] n —R a, where A=C 2 − to C 4 -alkylene, R a is H, a C l - to C 20 -alkyl group, -cycloalkyl group or -alkylaryl group; and n=2-250. 2. The method as claimed in claim 1 , wherein the copolymer comprises the gradient structure and a block structure comprising an essentially constant local concentration of monomers. 3. The method as claimed in claim 1 , wherein the copolymer comprises at least one further monomer unit MS of the formula III: where R 5′ and R 6′ , in each case independently, are H or an alkyl group having 1 to 5 carbon atoms, R 7′ is H, —COOM or an alkyl group having 1 to 5 carbon atoms, m′=0, 1 or 2, and p′=0 or 1; Y, in each case independently, is a chemical bond or —O—; Z, in each case independently, is a chemical bond, —O— or —NH—; R 9 , in each case independently, is an alkyl group, cycloalkyl group, alkylaryl group, aryl group, hydroxyalkyl group or acetoxyalkyl group, each having 1-20 carbon atoms. 4. The method as claimed in claim 1 , wherein the copolymer further comprises at least one first block A consisting of the ionizable monomer unit M1 and at least one second block B consisting of the side chain-bearing monomer unit M2. 5. The method as claimed in claim 1 , wherein the polydispersity of the copolymer is <1.5. 6. The method as claimed in claim 1 , wherein the molar ratio of the monomer units M1 to the monomer units M2 in the copolymer is in the range of 2-3.5. 7. The method as claimed in claim 1 , wherein R 1 =COOM; R 2 and R 5 , independently of one another, are H, —CH 3 or mixtures thereof; R 3 and R 6 , independently of one another, are H or —CH 3 , and where X in at least 75 mol % of all monomer units M2 is —O—. 8. The method as claimed in claim 1 , wherein the copolymer is prepared by a controlled free-radical polymerization and/or a living free-radical polymerization. 9. The method as claimed in claim 1 , wherein the copolymer is used for control of the setting characteristics of the binder composition. 10. The method as claimed in claim 1 , wherein all the copolymer present in the binder composition as a dispersant contains only monomer units that are selected from the group consisting of the ionizable monomer unit M1 and the side chain-bearing monomer unit M2.
containing calcium sulfate cements {(gypsum-paper plates E04C)} · CPC title
using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title
Use of a di- or tri-thiocarbonylthio compound, e.g. di- or tri-thioester, di- or tri-thiocarbamate, or a xanthate as chain transfer agent, e.g . Reversible Addition Fragmentation chain Transfer [RAFT] or Macromolecular Design via Interchange of Xanthates [MADIX] · CPC title
containing polyether side chains · CPC title
containing polyether side chains · CPC title
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