A polycarboxylate water reducer for improving the rheological properties of cement paste and its preparation method
A technology for rheological properties and cement slurry, which is applied in the field of polycarboxylate water reducing agent for improving the rheological properties of cement slurry and its preparation field, can solve the problems of reducing the anti-corrosion ability of concrete and reducing the strength of concrete, and achieves a space stabilization effect Significantly, improve rheology, and improve the effect of adsorption efficiency
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Embodiment 1
[0034] (1) transesterification reaction: 120.0gCH 3 (CH 2 ) 11 C 6 h 4 (OC 2 h 4 ) 20 OH, 25.0g methyl methacrylate, 0.90g polymerization inhibitor hydroquinone are mixed, under the protection of nitrogen, the temperature is raised to 40-60°C, then 2.15g catalyst 4-dimethylaminopyridine is added, and the temperature is raised to 80-90°C °C, keep the reaction temperature for 10 h, and cool down to room temperature after the reaction, to obtain the first mixture containing the esterification product and unreacted methyl methacrylate.
[0035] (2) Copolymerization reaction: Take 50.0g of the first mixture prepared in step (1), 80.0g of isobutylene alcohol polyoxyethylene ether with a molecular weight of 5000 and 330.0g of isobutenol polyoxyethylene ether with a molecular weight of 6000, 5.0g Hydroxyethyl methacrylate phosphate, 40.0g itaconic anhydride, 30.0g compound A (R 1 for -CH 2 , R 2 for CH 3, n is 100) and 200.0g of deionized water are added to the reaction ves...
Embodiment 2
[0038] (1) transesterification reaction: 144.0gCH 3 (CH 2 ) 7 C 6 h 4 (OC 2 h 4 ) 11 Mix OH, 54.0g methyl acrylate, and 1.22g polymerization inhibitor phenothiazine. Under nitrogen protection, heat up to 40-60°C, then add 3.25g catalyst dibutyltin oxide, heat up to 90-100°C, and keep warm for reaction After 8 hours, the temperature was lowered to room temperature after the reaction, and the first mixture containing the esterified product and unreacted methyl acrylate was obtained.
[0039] (2) Copolymerization reaction: 30.0g of the first mixture prepared in step (1), 500.0g of isobutyl alcohol polyoxyethylene ether with a molecular weight of 6000, 10.0g of hydroxyethyl methacrylate phosphate, 12g of acrylic acid, 20.0g of Compound A(R 1 for -CH 2 , R 2 is H, n is 50) and 300.0g deionized water are added to the reaction vessel and mixed, ammonium persulfate aqueous solution (wherein ammonium persulfate 3.52g, water 30.00g), isopropanol aqueous solution (wherein isopr...
Embodiment 3
[0042] (1) transesterification reaction: 180.0gCH 3 (CH 2 ) 8 C 6 h 4 (OC 2 h 4 ) 15 Mix OH, 47.0g methyl methacrylate, and 3.25g polymerization inhibitor diphenylamine. Under the protection of nitrogen, heat up to 40-60°C, then add 4.34g catalyst isopropyl titanate, heat up to 90-100°C, and keep warm. After reacting for 6 hours, the temperature was lowered to room temperature after the reaction, and the first mixture containing the esterified product and unreacted methyl methacrylate was obtained.
[0043] (2) Copolymerization reaction: 40.0g of the first mixture prepared in step (1), 100.0g of isobutylene alcohol polyoxyethylene ether with a molecular weight of 5000 and 200g of isobutenol polyoxyethylene ether with a molecular weight of 4000, 15.0g of Ethyl methacrylate phosphate, 22.0g methacrylic acid, 10.0g compound A (R 1 for -CH 2 CH 2 , R 2 for CH 3 , n is 20) and 200.0g deionized water are added to the reaction vessel and mixed, hydrogen peroxide aqueous s...
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