A kind of preparation method of solvent-resistant modified polyaryletherketone ultrafiltration membrane
A technology of polyaryletherketone and ultrafiltration membrane, which is applied in ultrafiltration, chemical instruments and methods, membranes, etc. It can solve the problems affecting membrane separation performance, swelling or even dissolution, and limiting application occasions, so as to improve the flux of pure water and thermal stability, improved stability, and the effect of a simple cross-linking method
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Embodiment 1
[0030](1) Add 2.7g polyaryletherketone (x=0.1, y=0.9) (18wt%), 2.25g PEG200 (15wt%) and 10.05g DMAc (N, N'-dimethylacetamide) and stirred at room temperature for 12 h. After vacuum degassing, use a 250 μm scraper to form a film on a clean glass plate and quickly immerse it in a coagulation bath. After the film is peeled off from the glass plate, take it out and place it in Soak in deionized water for 48 hours to remove additives.
[0031] (2) First, add 45 mL of absolute ethanol, 5 mL of 1 mol / L NaOH aqueous solution and 0.6 g of 1,4-dibromobutane into a 100 mL flask to prepare a cross-linking soaking solution.
[0032] (3) Then place the original membrane in the cross-linking soaking solution and heat soak at 60°C, take it out after 48 hours and wash it three times with absolute ethanol and deionized water to remove the cross-linking agent and catalyst on the surface of the membrane, and then place it in the deionized water. Soak in deionized water for later use.
[0033] (...
Embodiment 2
[0035] The difference between this embodiment and embodiment 1 is: the additive PEG2000.75g (5wt%) added in step 1, other steps and parameters are the same as embodiment 1.
Embodiment 3
[0037] The difference between this embodiment and embodiment 1 is that no additive PEG200 is added in step one, and other steps and parameters are the same as in embodiment 1.
[0038] Table 1 is the solvent resistance performance test result of the solvent-resistant modified polyaryletherketone ultrafiltration membrane prepared by the above-mentioned examples, wherein M1 and CL-M1, M2 and CL-M2, M3 and CL-M3 respectively represent embodiment 3, The original film and cross-linked film prepared in embodiment 2, embodiment 1.
[0039] Table 1
[0040]
[0041]
[0042] As shown in Table 1, the results show that the cross-linked film is very stable in non-polar solvents such as ethanol, and does not swell or dissolve at all; it has certain tolerance to polar aprotic solvents such as DMAc.
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Abstract
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