A kind of preparation method of highly adaptable concrete fluidity stabilizer
A concrete and adaptable technology, applied in the field of preparation of high-adaptability concrete fluidity stabilizer, can solve the problems of poor product stability, large difference in water reduction rate, general slump retention performance, etc. Good slump retention performance and good adaptability
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Embodiment 1
[0026] (1) Acylation esterification reaction: 346.00g maleic anhydride, 50.00g monoethanolamine, 30.40g o-hydroxybenzoic acid, 29.00g p-hydroxyphenylacetic acid, 1.00g hydroquinone and 1.00g phenothiazine were mixed, Under the protection of nitrogen, heat up to 65°C, then add 1.00g of periodic acid and 1.30g of dinitrobenzoic acid, heat up to 80°C, and keep warm for 3.0h. During this period, use vacuum or nitrogen with water to remove water, and react Down to room temperature after finishing, obtain the first mixture containing acylation product, esterification product and unreacted maleic anhydride;
[0027] (2) Monomer blending: Mix 8.00 g of the first mixture prepared in step (1), 1.20 g of sodium styrene sulfonate, and 100.00 g of APEG with a molecular weight of 2400, and add 90.00 g of water to dissolve it to obtain a copolymer monomer mixture solution;
[0028] (3) Copolymerization reaction: the above-mentioned comonomer mixture solution, hydrogen peroxide aqueous solut...
Embodiment 2
[0031] (1) Acylation esterification reaction: 144.00g acrylic acid, 172.00g methacrylic acid, 50.00g one isopropanolamine, 32.00g o-hydroxybenzoic acid, 45.00g o-hydroxymethylbenzoic acid, 0.60g hydroquinone Mix with 0.40g of diphenylamine, under the protection of nitrogen, heat up to 67°C, then add 1.00g of dinitrobenzoic acid and 2.00g of ethylenediaminetetraacetic acid, heat up to 90°C, keep the temperature for 2 hours, during this period use vacuum or ventilation The method of carrying water under nitrogen gas removes water, and after the reaction is completed, it is lowered to room temperature to obtain the first mixture containing acylated product, esterified product and unreacted acrylic acid and methacrylic acid;
[0032](2) Monomer blending: Mix 7.00 g of the first mixture prepared in step (1), 1.00 g of sodium allyl sulfonate, 1.30 g of sodium vinyl sulfonate and 100.00 g of HPEG with a molecular weight of 2400, and add 90.00 g of water to dissolve it to obtain a com...
Embodiment 3
[0036] (1) Acylation esterification reaction: 109.00g acrylic acid, 290.00g fumaric acid, 50.00g monoethanolamine, 41.00g p-hydroxyphenylacetic acid, 46.00g p-hydroxymethylbenzoic acid, 2.00g hydroquinone and 2.00g Mix diphenylamine, under the protection of nitrogen, heat up to 68°C, then add 2.00g of periodic acid and 2.00g of ethylenediaminetetraacetic acid, heat up to 95°C, keep warm for 1.0h, during this period, use vacuum or nitrogen with water The method removes water, cools down to room temperature after completion of the reaction, and obtains the first mixture containing acylation product, esterification product and unreacted acrylic acid and fumaric acid;
[0037] (2) Monomer blending: mix 5.00 g of the first mixture prepared in step (1), 1.00 g of sodium styrene sulfonate, 0.50 g of sodium methacrylate sulfonate, and 100.00 g of TPEG with a molecular weight of 2400, and add 90.00g water makes it dissolve, obtains comonomer mixture solution;
[0038] (3) Copolymeriza...
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