Preparation method of multifunctional resistance-reducing polymer suspension
A suspension and polymer technology, which is applied in the field of preparation of drag-reducing polymer suspensions, can solve the problems of poor drag-reducing effect of drag-reducing agents, and achieve good drag-reducing effects, stable properties, and convenient filling
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Embodiment 1
[0019] Embodiment 1 (comparative example)
[0020] 1) Preparation of α-olefin polymer:
[0021] Take 1000 g of 1-octene that has been refined and pre-cooled to 0 ° C, add 18 ml of 15% (mass) triethylaluminum n-hexane solution, stir at 0 ° C for 30 minutes, and then add TiCl 3 Catalyst 0.45g, mix well. As the reaction progresses, the viscosity of the reaction system increases gradually until the catalyst no longer precipitates, and then it is placed in a low-temperature environment (-20° C. to 30° C.) to react for 4 to 7 days. The weight average molecular weight of the polymer obtained in this way is about 4.6×10 6 , The monomer conversion rate of 1-octene is 95.2%, which is recorded as polymer A.
[0022] Take 1000 g of 1-octene and 1-decene (molar ratio 4:1) that has been refined and pre-cooled to 0 ° C, add 20 ml of 15% (mass) triethylaluminum-n-hexane solution, at 0 ° C Stir for 30 minutes, then add TiCl 3 Catalyst 0.5g, mix well. As the reaction progresses, the visco...
Embodiment 2
[0025] Embodiment 2 (comparative example)
[0026] 1) with embodiment 1;
[0027] 2) Take 30g of the synthesized α-olefin polymer B, coarsely crush it into particles smaller than 1 cm at room temperature, then add 20 g of ethylene-vinyl acetate with a diameter of about 6 mm, mix them and put them into a refrigerated low-temperature pulverizer In the environment of -130~-140°C, pulverize for 5 minutes to obtain a mixture powder larger than 80 mesh;
[0028] 3) Add 2g NP-7 nonionic surfactant, 0.01g silicone oil, 17g methanol, 30g purified water, 1g carboxymethyl cellulose (can be dissolved in water in advance) in the mixture powder of 2), in the mixer After stirring for 0.5-1 hour, a stable suspension product was finally formed, which was called sample II.
Embodiment 3
[0029] Embodiment 3 (invention example)
[0030] 1) with embodiment 1;
[0031] 2) Take 40 g of the α-olefin polymer B synthesized in Example 1, add 13 g of ethylene-vinyl acetate, 13 g of polyoctearyl acrylate, and 6.5 g of polyalkenyl succinimide, and they are first coarsely crushed at room temperature into particles smaller than 1 cm, then mix them and put them into a refrigerated low-temperature pulverizer, and pulverize them for 6 minutes at an environment of less than -130 to -140 ° C to obtain a free-flowing mixture powder greater than 80 meshes;
[0032] 3) Add 3g NP-10, 0.01g simethicone, 16g methanol, 40g purified water, 0.7g carboxymethyl cellulose (can be dissolved in water in advance) to the mixture powder in 2), and stir in the mixer for 0.5 After ~1 hour, a stable suspension product was finally formed, referred to as Sample III.
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