Processes for forming permanent hydrophilic porous coatings onto a substrate, and porous membranes thereof
A porous membrane, permanent technology, applied in coatings, chemical instruments and methods, membranes, etc., can solve problems such as ineffectiveness
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Embodiment 1
[0050] In this example, a functionalized PVA was synthesized and referred to as PVA-MMA(2.4)-high MW. PVA (20.1 g, 456 mmol, Celvol 165 from Celanese Ltd.) was added to a 500 mL round bottom flask along with anhydrous DMSO (175 mL) and stirred vigorously at 75 °C until a homogeneous solution was obtained. The reaction was cooled to 40°C and 2-isocyanatoethyl methacrylate (3.53 g, 22.8 mmol) was slowly added to the vigorously stirred solution. The viscous solution was stirred for 24 hours, then cooled to room temperature. The polymer was precipitated into a 5:1 mixture of isopropanol:ether (total 800 mL). The fluffy white solid was dried under vacuum at room temperature. 1 H NMR showed that about 2.4% of the repeat units contained the graftable methacrylate linkage (21.5 g, 91% yield, 42% conversion).
Embodiment 2
[0051] In this example, a functionalized PVA was synthesized and referred to as PVA-MMA(5.0)-high MW. PVA (20.1 g, 456 mmol, Celvol 165 from Celanese Ltd.) along with anhydrous DMSO (150 mL) was added to a 500 mL three necked round bottom flask and stirred vigorously at 95°C until a homogeneous solution was obtained. The reaction was cooled to room temperature and 2-isocyanatoethyl methacrylate (10.1 g, 65.1 mmol) was slowly added to the vigorously stirred solution in an ice bath to control any exotherm. The viscous solution was stirred at 40°C for 24 hours, then cooled to room temperature. The polymer was precipitated into a 3:1 mixture of isopropanol:ether (700 mL total). The fluffy white solid was dried under vacuum at room temperature. 1 H NMR showed that about 5% of the repeat units contained the graftable methacrylate linkages (24.0 g, 80% yield, 39% conversion).
Embodiment 3
[0052] In this example, a functionalized PVA was synthesized and referred to as PVA-MMA(1.4)-high MW. PVA (20.0 g, 454 mmol, Celvol 165 from Celanese Ltd.) was added to a 500 mL round bottom flask along with DMSO (200 mL) and stirred vigorously at 75°C until a homogeneous solution was obtained. The reaction was cooled to 45 °C, 4-(dimethylamino)pyridine (2.22 g, 18.2 mmol) and 2-isocyanatoethyl methacrylate (1.41 g, 9.09 mmol) were slowly added to the vigorously stirred in the solution. The viscous solution was stirred for 24 hours, then cooled to room temperature. The polymer was precipitated into isopropanol (1200 mL total). The fluffy white solid was dried under vacuum at 40°C. 1 H NMR showed that about 1.4% of the repeat units contained the graftable methacrylate linkages (20.8 g, 97% yield, 70% conversion).
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