Preparation method of high-molecular-weight hydrophobic cationic polyacrylamide
A polyacrylamide and cationic technology, which is applied in the field of preparation of high molecular weight hydrophobic cationic polyacrylamide, can solve the problems of poor solubility, poor solubility, low molecular weight, etc., achieve stable polymerization reaction, fast dissolution speed, and use convenient effect
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Embodiment 1)
[0020] The preparation method of the high molecular weight hydrophobic cationic polyacrylamide of the present embodiment comprises the following steps:
[0021] ①Weighing monomers including acrylamide (CAS NO.79-06-1), acryloyloxyethyltrimethylammonium chloride (CAS NO.46830-22-2) and octadecyl acrylate (CAS NO.4813 -57-4) For standby, the ratio of the amount of the above three monomers is (47~189.5): (10~50): (0.5~3); the sum of the mass of the above three monomers is recorded as the unit total body weight.
[0022] In this example, 37.7g (0.53mol) of acrylamide, 11.3g (0.059mol) of acryloyloxyethyltrimethylammonium chloride and 0.9g (0.0028mol) of octadecyl acrylate were weighed for use; the above three monomers The ratio of the amount of substances is 189:21:1.
[0023] ②Put the acrylamide and acryloyloxyethyltrimethylammonium chloride weighed in step ① into the reaction vessel with a water bath in sequence, and control the temperature of the water bath at 5°C to 10°C (in...
Embodiment 2)
[0032]All the other preparation methods of the present embodiment are the same as in Example 1, except that:
[0033] In step ①, weigh 42.9g (0.60mol) of acrylamide, 29.6g (0.15mol) of acryloyloxyethyltrimethylammonium chloride and 2.5g (0.0077mol) of stearyl acrylate for later use.
[0034] In step ②, add 225 g of deionized water into the reaction vessel, stir at a stirring speed of 54 rpm, and stir for 12 minutes.
[0035] In step ③, the amount of cetyltrimethylammonium bromide added is 2.25 g, and the stirring speed is 85 rpm.
[0036] The stirring speed in step ④ is 122 rpm, stirring for 18 minutes.
[0037] Step 5. The addition of urea is 0.12g, the addition of dimethylaminoethyl methacrylate is 0.03g; the stirring speed is 122 rpm.
[0038] Step 6. the add-on of ammonium persulfate is 0.045g, the add-on of sodium bisulfite is 0.015g, and the add-on of 2,2'-azo (2-amidinopropane) dihydrochloride is 0.015g.
Embodiment 3)
[0040] All the other preparation methods of the present embodiment are the same as in Example 1, except that:
[0041] In step ①, weigh 73.9g (1.03mol) of acrylamide, 36.9g (0.19mol) of acryloyloxyethyltrimethylammonium chloride and 4.2g (0.013mol) of octadecyl acrylate for later use.
[0042] In step ②, add 385 g of deionized water into the reaction vessel, and the stirring speed is 60 rpm.
[0043] In step ③, the amount of cetyltrimethylammonium bromide added is 2.3 g, and the stirring speed is 90 rpm.
[0044] The stirring speed in step ④ is 125 rpm, stirring for 20 minutes.
[0045] The add-on of urea in step ⑤ is 0.086g, the add-on of dimethylaminoethyl methacrylate is 0.029g; Stirring speed is 125 rpm.
[0046] Step 6. the add-on of ammonium persulfate is 0.069g, the add-on of sodium bisulfite is 0.023g, and the add-on of 2,2'-azo (2-amidinopropane) dihydrochloride is 0.023g.
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