Method for preparing polyvinylidene fluoride-phenolphthalein polyethersulfone blending membrane
A technology of phenolphthalein-based polyethersulfone and polyvinylidene fluoride, which is applied in the field of preparation of polyvinylidene fluoride membranes, can solve problems such as inability to solve shrinkage resistance and hydrophobicity, limit the application of PVDF membranes, and expensive diphenyl carbonate, etc. , achieve good application prospects, improve shrinkage resistance and high strength
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Embodiment 1
[0025] Blend polyvinylidene fluoride with an intrinsic viscosity of 1.67, phenolphthalein-based polyethersulfone with a molecular weight of 50,000, lithium chloride, dibutyl phthalate and dimethylacetamide, and its mass fraction is composed of polyvinylidene fluoride Ethylene 21.6%, phenolphthalein polyethersulfone 2.4%, lithium chloride 1%, dibutyl phthalate 55%, dimethylacetamide 20%. The mixture was heated to 130°C, stirred for 1 hour, and then allowed to stand at 130°C for 2 hours. The blended solution was directly scraped on the support material to form a flat film, the thickness of which was controlled to 200 microns, and the film was solidified by immersing in a water bath at 30°C. The cured film was first immersed in ethanol for extraction for 12 hours, then immersed in distilled water for 12 hours, then immersed in 50% ethylene glycol aqueous solution for 6 hours, and finally dried at 60°C.
[0026] The compressive strength of the membrane is greater than 5MPa, and t...
Embodiment 2
[0028] Blend polyvinylidene fluoride with an intrinsic viscosity of 1.67, phenolphthalein-based polyethersulfone with a molecular weight of 50,000, lithium chloride, dibutyl phthalate and dimethylacetamide, and its mass fraction is composed of polyvinylidene fluoride Ethylene 21.6%, phenolphthalein polyethersulfone 2.4%, lithium chloride 1%, dibutyl phthalate 65%, dimethylacetamide 10%. The mixture was heated to 130°C, stirred for 1 hour, and then allowed to stand at 130°C for 2 hours. The blended solution was passed through a hollow spinneret to make a hollow fiber membrane with a membrane thickness of 280 microns. The cured film was first immersed in ethanol for extraction for 12 hours, then immersed in distilled water for 12 hours, then immersed in 50% ethylene glycol aqueous solution for 6 hours, and finally dried at 60°C.
[0029] The compressive strength of the hollow fiber membrane is greater than 5MPa, and the pure water flux at 0.1MPa is 1184L / (m 2 .h).
Embodiment 3
[0031] Blend polyvinylidene fluoride with an intrinsic viscosity of 1.67, phenolphthalein-based polyethersulfone with a molecular weight of 50,000, polyvinylpyrrolidone, dibutyl phthalate and dimethylacetamide, and its mass fraction is composed of polyvinylidene fluoride Ethylene 18%, phenolphthalein polyethersulfone 2%, polyvinylpyrrolidone 5%, dibutyl phthalate 65%, dimethylacetamide 10%. The mixture was heated to 130°C, stirred for 1 hour, and then allowed to stand at 130°C for 2 hours. The blended solution was directly scraped on the support material to form a flat film, the thickness of which was controlled to 200 microns, and the film was solidified by immersing in a water bath at 30°C. The cured film was first immersed in ethanol for extraction for 12 hours, then immersed in distilled water for 12 hours, then immersed in 50% ethylene glycol aqueous solution for 6 hours, and finally dried at 60°C.
[0032] The compressive strength of the membrane is greater than 5MPa, a...
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