Non-dewetting porous membranes
一种亲水性基团、氟碳的技术,应用在膜、膜技术、半透膜分离等方向,能够解决薄多孔膜破裂、昂贵、密封孔膜耗时等问题
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[0135] General Synthetic Methods and Test Procedures
[0136] A fluorocarbon liquid composition comprising from about 0.4 wt% to about 4 wt% of one or more fluorinated ionomers having an equivalent weight of from about 380 g / equivalent to about 620 g / equivalent (as in Table 3 of Example 2 described in ) to coat microporous membrane supports. Fluorinated ionomers derived from CF 2 = CF-O-CF 2 CF 2 SO 2 F monomer unit, tetrafluoroethylene, formula CH 2 =CH-(CF 2 ) 6 -CH=CH 2 The diene unit and iodinated chain transfer agent I-(CF 2 ) 4 -I. Dissolve the ionomer in a fluorocarbon solvent such as methyl perfluorobutyl ether (Novik TM HFE-7100), perfluoropolyether solvents (such as glue SV90) or a combination of these. These ionomer solutions were obtained from Solvay Sulex and optionally filtered prior to use using a filtration microporous membrane of 0.45 micron, 0.2 micron or smaller nominal pore size. Non-limiting examples of combinations of ionomers, free radica...
example 1
[0158] According to the emulsion polymerization procedure disclosed in U.S. Patent No. 6,902,676, by combining TFE with formula CF 2 = CF-O-CF 2 CF 2 -SO 2 Copolymerize vinyl ethers of F to obtain copolymers using the formula CH 2 CH-C 6 f 12 -CHCH 2 Diolefins as pre-crosslinkers, using I-C 4 f 8 -I as chain transfer agent and potassium persulfate as free radical initiator. Copolymers C1, C2, C3 and C4 were obtained under the following conditions shown in Table 2:
[0159] Table 2. Conditions for obtaining copolymers C1, C2, C3 and C4.
[0160]
example 2
[0162] This example discloses the preparation of a fluorinated ionomer coating solution for use in forms of the invention. The pre-crosslinked perfluoroionomer (with iodine chain ends) prepared in Example 1 was dissolved in a partially fluorinated or perfluorinated solvent to achieve a final concentration of about 4 wt%. The mixture was then centrifuged at 10,000 rpm for two hours. A solution S2 * Centrifuge for an additional two hours at 20,000 rpm. A clear transparent liquid was obtained after removal of the insoluble residue, which exhibited the physical properties summarized in Table 3 below:
[0163] Table 3. Solutions S1, S2, S2 * , physical properties of S3 and S4.
[0164]
[0165] After dissolving 40 mg of the copolymer in 0.6 ml of hexafluorobenzene, the molar percentage of comonomer was determined by means of NMR and the equivalent weight was subsequently calculated.
[0166] The iodine content of the ionomer was measured by X-ray fluorescence (XRF) and meas...
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