Preparation method of a low-sensitivity concrete fluidity stabilizer
A concrete and fluidity technology, which is applied in the field of preparation of low-sensitivity concrete fluidity stabilizers, can solve the problems of inability to maintain stable concrete fluidity, high dosage of water reducing agent, high cost of use, etc., and achieve high double bond retention rate , low esterification temperature, and the effect of reducing production energy consumption
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Embodiment 1
[0023] (1) Esterification: 230.00g maleic anhydride, 200.00g molecular weight polyethylene glycol monomethyl ether of 600, 27.60g p-hydroxybenzoic acid, 57.30g o-hydroxyphenylacetic acid, 1.00g hydroquinone and 1.00 Mix g phenothiazine, under the protection of nitrogen, heat up to 65°C, then add 1.00g of periodic acid and 1.70g of dinitrobenzoic acid, heat up to 78°C, keep warm for 0.5h, during this period use vacuum or nitrogen belt The method of water is removed water, is down to room temperature after reaction finishes, obtains the first mixture that contains esterification product and unreacted maleic anhydride;
[0024] (2) Monomer blending: 200.00 g of the first mixture prepared in step (1) was mixed with 1.50 g of sodium styrene sulfonate, and 150.00 g of water was added to dissolve it to obtain a comonomer mixture solution;
[0025] (3) Copolymerization reaction: the above-mentioned comonomer mixture solution, hydrogen peroxide aqueous solution (wherein hydrogen peroxi...
Embodiment 2
[0028] (1) Esterification reaction: 72.00g acrylic acid, 91.00g methacrylic acid, 200.00g polyethylene glycol monomethyl ether with a molecular weight of 800, 27.60g o-hydroxybenzoic acid, 38.00g p-hydroxymethylbenzoic acid, 1.60g Mix hydroquinone and 0.70g diphenylamine, under the protection of nitrogen, heat up to 70°C, then add 2.00g dinitrobenzoic acid and 2.00g ethylenediaminetetraacetic acid, heat up to 96°C, keep warm for 3 hours, during which Vacuumize or pass nitrogen with water to remove water, and after the reaction is finished, drop to room temperature to obtain the first mixture containing esterification product and unreacted acrylic acid and methacrylic acid;
[0029] (2) Monomer blending: Mix 200.00 g of the first mixture prepared in step (1), 1.00 g of sodium allyl sulfonate and 1.00 g of sodium vinyl sulfonate, and add 150.00 g of water to dissolve it to obtain a copolymer monomer mixture solution;
[0030] (3) Copolymerization reaction: the above-mentioned c...
Embodiment 3
[0033](1) Esterification reaction: 72.00g acrylic acid, 163.00g fumaric acid, 200.00g polyethylene glycol monomethyl ether with a molecular weight of 1000, 18.30g p-hydroxyphenylacetic acid, 36.50g m-hydroxymethylbenzoic acid, 2.00g Mix hydroquinone and 1.00g of diphenylamine, under the protection of nitrogen, heat up to 67°C, then add 3.00g of periodic acid and 2.00g of ethylenediaminetetraacetic acid, heat up to 80°C, keep warm for 1.0h, use pumping Remove water by vacuum or through nitrogen with water, and cool to room temperature after the reaction to obtain the first mixture containing esterification product and unreacted acrylic acid and fumaric acid;
[0034] (2) Monomer blending: 200.00 g of the first mixture prepared in step (1) was mixed with 1.00 g of sodium styrene sulfonate and 1.50 g of sodium methacrylate sulfonate, and 150.00 g of water was added to dissolve it to obtain comonomer mixture solution;
[0035] (3) Copolymerization reaction: the above-mentioned co...
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