Use of CSH suspensions in well cementing
US-9409820-B2 · Aug 9, 2016 · US
US12378159B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12378159-B2 |
| Application number | US-202017766276-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 25, 2020 |
| Priority date | Nov 29, 2019 |
| Publication date | Aug 5, 2025 |
| Grant date | Aug 5, 2025 |
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The invention relates to the use of branched copolymers as dispersants of mineral binders, wherein the copolymers are formed from (1) at least one olefinically unsaturated carboxylic acid monomer (2) at least one olefinically unsaturated macromonomer of the general structure (I) where R 1 is an olefinically unsaturated radical which has 2-10 carbon atoms and may optionally be substituted by oxygen and/or nitrogen, preferably vinyl, allyl, methallyl, vinyloxybutyl, isoprenyl, acryloyl and/or methacryloyl, X=O or NH, A is in each case independently C1-C10 alkylene, preferably ethylene, propylene and/or butylene, R 2 =C1-C16 alkyl, B is in each case independently C1-C10 alkylene, preferably ethylene, propylene and/or butylene, m is in each case independently an integer in the range of 0-350, preferably 2-200, more preferably 5-150, especially 7-30, n is an integer in the range of 0-100, preferably 1-100, more preferably 2-75, most preferably 5-55, p is 0 or 1, preferably 0, o is an integer in the range of 1-50, preferably 3-40, more preferably 6-30, especially 8-20, and q is an integer in the range of 1-10.
Opening claim text (preview).
The invention claimed is: 1. A copolymer, the copolymer having repeating units formed from (1) at least one olefinically unsaturated carboxylic acid monomer, and (2) at least one olefinically unsaturated macromonomer of the general structure (I) where R 1 is an olefinically unsaturated radical which has 2-10 carbon atoms and may optionally be substituted by oxygen and/or nitrogen, X is O or NH, A is in each case independently a C1-C10 alkylene, R 2 is a C1-C16 alkyl, B is in each case independently a C1-C10 alkylene, m is in each case independently an integer in the range of 2-200, n is an integer in the range of 0-100, p is 0 or 1, o is an integer in the range of 1-50, and q is an integer in the range of 2-10. 2. The copolymer as claimed in claim 1 , wherein the at least one unsaturated carboxylic acid monomer is a monomer of the general structures (IIa) or (IIb) where R 3 is a H or a C1-C6-alkyl chain, R 4 is a H, C(O)Y, or a C1-C6-alkyl chain, and Y is OM, with M selected from H, alkali metals, alkaline earth metals or organic ammonium, or Y is NR 4 R 5 with R 4 and R 5 independently being H or a C1-C6-alkyl chain; where Z is O or NR 5 and R 3 has the definitions as above, and R 5 is a H or a C1-C6-alkyl chain. 3. The copolymer as claimed in claim 1 , wherein in the general structure (I), X is O, p is 0, m is in each case independently an integer in the range of 5-150, n is an integer in the range of 5-55, and o is an integer in the range of 8-50. 4. The copolymer as claimed in claim 1 , wherein the proportion of ethylene oxide units in the polyalkylene oxide chains (AO) n and (BO) m , based on all alkylene oxide units AO and BO present, is more than 90 mol %. 5. The copolymer as claimed in claim 1 , wherein the molar ratio of the at least one olefinically unsaturated carboxylic acid monomer to the at least one olefinically unsaturated macromonomer of the general structure (I) is in the range of 0.3-30. 6. The copolymer as claimed in claim 1 , wherein the copolymer further comprises at least one additional repeating unit formed from a monomer M selected from the group consisting of styrene, ethylene, propylene, butylene, butadiene, isoprene, vinyl acetate, vinyl chloride, acrylonitrile, N-vinylpyrrolidone, hydroxyalkyl (meth) acrylates and a monomer of the general structure (VI) where R 6 is in each case independently H, —CH 2 —COOM or an alkyl group having 1 to 5 carbon atoms, R 7 is in each case independently H or an alkyl group having 1 to 5 carbon atoms, R 8 is in each case independently H, —COOM or an alkyl group having 1 to 5 carbon atoms, r is 0, 1 or 2, s is 0 or 1, t is 0, or an integer from 1 to 4, u=2-250, X, in each case independently, is —O—or —NH—, R 9 is in each case independently H, a C 1 to C 20 alkyl group, cyclohexyl group or alkylaryl group, and D is a C 2 to C 4 alkylene. 7. A composition comprising: at least one mineral binder and at least one copolymer as claimed in claim 1 , wherein the at least one copolymer is present in the composition in an amount effective to act as a dispersant for the at least one mineral binder, and an average molar mass Mw of the at least one copolymer is in the range of 1,000-1,000,000 g/mol. 8. The composition as claimed in claim 7 , wherein the at least one mineral binder is selected from the group consisting of cement, portland cement, aluminate cement, α-calcium sulfate hemihydrate, β-calcium sulfate hemihydrate, anhydrite, lime, industrial slags, synthetic slags, blast furnace slags, foundry sand, foundry sand flour, electrothermal phosphorus slags, copper slags, stainless steel slags, pozzolans, fly ashes, microsilica, metakaolin, natural pozzolans, tuff, trass, volcanic ash, natural zeolites, synthetic zeolites, and burnt oil shale. 9. The composition as claimed in claim 7 , wherein the at least one copolymer is present in an amount of 0.01-10% by weight based on the content of the at least one mineral binder. 10. A multistage process for preparing the copolymer as claimed in claim 1 , comprising the steps of 1) forming a first reaction product by reacting an alcohol or amine R 1 —XH with alkylene oxide and/or a halogenated alcohol or amine Hal-R 2 —XH, where R 1 is an olefinically unsaturated radical which has 2-10 carbon atoms and may optionally be substituted by oxygen and/or nitrogen, X is O or NH, Hal is a halide and R 2 is a C 1 -C 16 alkyl, 2) forming a second reaction product by reacting the first reaction product from step 1) with glycidol or epichlorohydrin or a mixture of glycidol and alkylene oxide or epichlorohydrin and alkylene oxide, 3) forming a third reaction product by reacting the second reaction product from step 2) with alkylene oxide, and 4) forming a fourth reaction product by free-radically polymerizing a mixture of at least one olefinically unsaturated carboxylic acid monomer with the third reaction product from step 3). 11. The multistage process as claimed in claim 10 , further comprising 5) drying the fourth reaction product from step 4). 12. A mineral binder or mineral binder composition comprising at least one mineral binder, and at least one copolymer obtained from the multistage process as claimed in claim 10 . 13. The mineral binder or mineral binder composition as claimed in claim 12 , comprising 0.01-10% by weight, based on the content of the at least one mineral binder, of the at least one copolymer obtained from a multistage process comprising the steps of 1) forming a first reaction product by reacting an alcohol or amine R 1 —XH with alkylene oxide and/or a halogenated alcohol or amine Hal-R 2 —XH, where R 1 is an olefinically unsaturated radical which has 2-10 carbon atoms and may optionally be substituted by oxygen and/or nitrogen, X is O or NH, Hal is a halide and R 2 is a C 1 -C 16 alkyl, 2) forming a second reaction product by reacting the first reaction product from step 1) with glycidol or epichlorohydrin or a mixture of glycidol and alkylene oxide or epichlorohydrin and alkylene oxide, 3) forming a third reaction product by reacting the second reaction product from step 2) with alkylene oxide, and 4) free-radically polymerizing a mixture of at least one olefinically unsaturated carboxylic acid monomer with the third reaction product from step 3). 14. An additive for mineral binder compositions, comprising at least one copolymer obtained from the multistage process as claimed in claim 10 . 15. The additive as claimed in claim 14 , further comprising one or more polycarboxylate ethers. 16. A shaped body obtained by curing the mineral binder or the mineral binder composition as claimed in claim 12 .
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