Preparation method of novel ultrahigh-viscosity anionic polyacrylamide
A technology of polyacrylamide and acrylamide, which is applied in the field of preparation of new ultra-high viscosity anionic polyacrylamide, which can solve problems such as difficult to continue to increase significantly, PAM viscosity bottleneck, etc., and achieve good mechanical shear resistance and good viscosity recovery ability , good effect of salt resistance
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Embodiment 1
[0010] The parts by weight of raw materials are: 210 parts by weight of acrylamide, 90 parts by sodium α-allyl sulfonate, 10 parts by sodium acrylate, 1.5 parts by structure regulator, 620 parts by weight of deionized water, 0.012 parts by weight of potassium persulfate, and 0.008 parts by weight of sodium bisulfite.
[0011] The specific preparation process is:
[0012] (1) Add deionized water, acrylamide, sodium α-allyl sulfonate, sodium acrylate, structure modifier, and initiator into the reactor. After mixing evenly, adjust the pH value to between 4 and 5 with acrylic acid;
[0013] (2) Deoxygenate with nitrogen for 30 minutes, add an initiator and polymerize at 2°C;
[0014] (3) After the reaction, take out the jelly, granulate the rubber block, and place the rubber granule in an oven at 75°C for drying;
[0015] (4) After 2 hours, the dried colloidal particles were taken out and pulverized to obtain the product. The viscosity of the product was 810 cps.
Embodiment 2
[0017] The parts by weight of raw materials are: 240 parts by weight of acrylamide, 120 parts of sodium α-allyl sulfonate, 15 parts of sodium acrylate, 3 parts of structure regulator, 680 parts of deionized water, 0.027 parts of potassium persulfate, and 0.018 parts of sodium bisulfite.
[0018] The specific preparation process is:
[0019] (1) Add deionized water, acrylamide, sodium α-allyl sulfonate, sodium acrylate, structure modifier, and initiator into the reactor. After mixing evenly, adjust the pH value to between 4 and 5 with acrylic acid;
[0020] (2) Deoxygenate with nitrogen for 30 minutes, add an initiator and polymerize at 2°C;
[0021] (3) After the reaction, take out the jelly, granulate the rubber block, and place the rubber granule in an oven at 75°C for drying;
[0022] (4) After 2 hours, the dried colloidal particles were taken out and pulverized to obtain the product with a viscosity of 860 cps.
Embodiment 3
[0024] The parts by weight of raw materials are: 270 parts by weight of acrylamide, 160 parts by sodium α-allylsulfonate, 22 parts by sodium acrylate, 6 parts by structure modifier, 700 parts by weight of deionized water, 0.042 parts by potassium persulfate, and 0.021 parts by sodium bisulfite.
[0025] The specific preparation process is:
[0026] (1) Add deionized water, acrylamide, sodium α-allyl sulfonate, sodium acrylate, structure modifier, and initiator into the reactor. After mixing evenly, adjust the pH value to between 4 and 5 with acrylic acid;
[0027] (2) Deoxygenate with nitrogen for 30 minutes, add an initiator and polymerize at 2°C;
[0028] (3) After the reaction, take out the jelly, granulate the rubber block, and place the rubber granule in an oven at 75°C for drying;
[0029] (4) After 2 hours, the dried colloidal particles were taken out and pulverized to obtain the product with a viscosity of 900 cps.
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