Preparation method of heat-resistance and salt-tolerance polyacrylamide
A technology of polyacrylamide and acrylamide, which is applied in the field of functional polymers, can solve problems such as poor viscosity increasing effect and increased degree of hydrolysis, and achieve good solubility and filterability, convenient polymerization operation, and favorable production effects
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Embodiment 1
[0017] In a 500ml jar, first add 230g of acrylamide aqueous solution with a mass concentration of 25%, 1.0g of pure acrylic acid, and 1.15g of AMPS, then control the temperature within 15°C, and adjust the pH with sodium hydroxide liquid alkali while stirring =6.1. After cooling down to 1°C, high-purity nitrogen (nitrogen purity ≥ 99.99%) was introduced to remove oxygen in the system. When the oxygen content of the system is less than 0.01%, add 0.003g of disodium ethylenediaminetetraacetic acid complexing agent; 0.06g of azo compound azobisisobutyronitrile; 0.005g of high-efficiency chain transfer agent sodium formate; Initiator triethanolamine 0.0005g; oxidation initiator tert-butyl hydroperoxide 0.00022g, seal and seal after reaction. When the temperature of the reaction no longer rises, it is placed in a water bath at 80° C. for 1 hour. After the heat preservation, take out the colloid and mince it, add 20ml of liquid caustic soda (mass fraction 30%), and hydrolyze at 85...
Embodiment 2
[0020] In a 500ml jar, first add 230g of acrylamide aqueous solution with a mass concentration of 25%, 1.0g of pure acrylic acid, and 1.50g of AMPS, then control the temperature within 15°C, and adjust the pH with sodium hydroxide liquid alkali while stirring =6.4. After cooling down to 1°C, high-purity nitrogen (nitrogen purity ≥ 99.99%) was introduced to remove oxygen in the system. When the oxygen content of the system is less than 0.01%, 0.009 g of the complexing agent tetrasodium ethylenediaminetetraacetic acid; 0.10 g of the azo compound azobisisobutyronitrile; g; reduction initiator sodium metabisulfite 0.0008g; oxidation initiator dialkyl peroxide 0.0003g, sealed after the reaction. When the temperature of the reaction no longer rises, it is placed in a water bath at 80° C. for 1 hour. After the heat preservation, take out the colloid and mince it, add 20ml of liquid caustic soda (mass fraction 30%), and hydrolyze at 85°C for 1h. Finally, the rubber block is dried i...
Embodiment 3
[0023] In a 500ml jar, first add 230g of acrylamide aqueous solution with a mass concentration of 25%, 1.0g of pure acrylic acid, and 3.40g of AMPS, then control the temperature within 15°C, and adjust the pH with sodium hydroxide liquid alkali while stirring =5.9. After cooling down to 1°C, high-purity nitrogen (nitrogen purity ≥ 99.99%) was introduced to remove oxygen in the system. When the oxygen content of the system is less than 0.01%, add 0.005g of complexing agent disodium ethylenediaminetetraacetic acid, 0.08g of azo compound azobisisoheptanonitrile, and 0.010g of high-efficiency chain transfer agent isopropanol every 3 minutes Reduction initiator ferrous chloride 0.0008g; Oxidation initiator hydrogen peroxide 0.0003g, carry out sealing after reaction. When the temperature of the reaction no longer rises, it is placed in a water bath at 80° C. for 1 hour. After the heat preservation, take out the colloid and mince it, add 20ml of liquid caustic soda (mass fraction 3...
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