초록

Porous hydrophilic membranes comprising a porous inert support on which an ionomer is deposited, said membranes being characterized in that they have a water permeability higher than 1 l/(h.m2.Atm).

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1. Porous hydrophilic membranes comprising a porous inert support on which at least one ionomer is deposited, wherein the membranes have a water permeability higher than 1 l(h.m2.Atm), and wherein the ionomer is amorphous and comprises acid hydrophilic groups.2. Membranes according to claim 1, compr

1. Porous hydrophilic membranes comprising a porous inert support on which at least one ionomer is deposited, wherein the membranes have a water permeability higher than 1 l(h.m2.Atm), and wherein the ionomer is amorphous and comprises acid hydrophilic groups.2. Membranes according to claim 1, comprising pores partially or totally occluded to gases.3. Membranes according to claim 2, comprising pores totally occluded to gases and an ionomer amount higher than about 30% by weight.4. Membranes according to claim 2, comprising pores totally occluded to gases and an ionomer amount higher than about 20% by weight.5. A method of dehydrating humid gases comprising contacting said gases with the membranes of claim 4.6. The method of claim 5, wherein the method of dehydrating is pervaporation.7. Membranes according to claim 1, wherein the porous inert support is formed by (per)fluoropolymers.8. Membranes according to claim 1, wherein the ionomer is a (per)fluorinated polymer comprising ?SO3H and/or ?COOH.9. Membranes according to claim 8, wherein the ionomer comprises:(A) monomeric units deriving from one or more fluorinated monomers containing at least an ethylene unsaturation; or (B) fluorinated monomeric units containing functional groups selected from the group consisting of one or more of ?SO2F, ?COOR, and ?COF, wherein R is a C1 to C20 alkyl radical or a C6 to C20 aryl radical, and wherein the functional groups are converted into one or more of hydrophilic groups ?SO3H or ?COOH in the final membrane. 10. Membranes according to claim 9, the fluorinated monomeric units (A) are selected from the group consisting of:vinylidene fluoride (VDF); C2 to C8 perfluoroolefins; C2 to C8 chloro, bromo- and/or iodo-fluoroolefins: CF2?CFOR1 (per)fluoroalkylvinylethers (PAVE), wherein Rf is a C1 to C6 (per)fluoroalkyl; and CF2?CFOX perfluoro-oxyalkylvinylethers, wherein X is a C1 to C12 perfluoro-oxyalkyl having one or more ether groups. 11. Membranes according to claim 9, wherein the fluorinated monomeric units (B) are selected from the group consisting of:F2C?CF?O?CF2?CF2?SO2F; F2C?CF?O?[CF2?CXF?O]n?CF2?CF2?SO2F, wherein X=Cl, F or CF3 and n=1 to 10; F2C?CF?O?CF2?CF2?CF2?SO2F; F2C?CF?Ar?SO2F wherein Ar is an aryl ring; F2C?CF?O?CF2?CF2?CF2?COF; and F2C?CF?O?[CF2?CXF?O]n?CF2?CFX?COF, wherein X=Cl, F or CF3 and n=1 to 10. 12. Membranes according to claim 8, wherein the (per)fluorinated ionomer is crosslinked.13. Membranes according to claim 1, wherein the ionomer contains from 0.01% to 5% by moles of monomeric units deriving from a bis-olefin of formula:R1R2C?CH?(CF2)m?CH?CR5R6??(I) wherein:m=2 to 10; and R1, R2, R5, and R6 are equal to or different from each other and are H or C1 to C5 alkyl groups. 14. Membranes according to claim 1, wherein the at least one ionomer is selected from the group consisting of one or more of the following monomers:monomeric units deriving from TFE; monomeric units deriving from CF2?CF?O?CF2CF2SO2F; monomeric units deriving from the bis-olefin of formula (I); and iodine atoms in end position. 15. Membranes according to claim 1, wherein the ionomer shows a substantial absence of crystallinity.16. Membranes according to claim 15, wherein the ionomer has a residual crystallinity lower than 5%.17. Membranes according to claim 1, containing, besides the amorphous ionomer comprising acid hydrophilic groups, one or more amorphous or crystalline (per)fluoropolymers, wherein the amorphous (per)fluoropolymers are one or more (per)fluoroelastomers selected from one or more of the group consisting of TFE/(per)fluorovinylether copolymers, TFE/VDF/HFP, and (per)fluorovinylether.18. Membranes according to claim 17, wherein the (per)fluoropolymers are of crystalline ionomeric type.19. A method of separating water from aqueous solutions, by contacting said solutions with the membranes according to claim 1.20. The method according to claim 19, wherein the method is iperfiltration or reverse osmosis and wherein the membranes comprise pores totally occluded to gases and contain an ionomer amount higher than about 30% by weight.21. A process for preparing hydrophilic porous membranes according to claim 1, comprising a porous support formed by a (per)fluorinated polymer, and amorphous (per)fluorinated ionomers containing hydrophilic groups, selected from the group consisting of ?SO3H and ?COOH, said process comprising:a) impregnating the porous support with a (per)fluorinated ionomer solution in fluorinated organic solvent, ?wherein: the (per)fluorinated ionomer comprises hydrolyzable groups, selected from the group consisting of ?SO2F, ?COOR, and ?COF, wherein R is a C1 to C20 alkyl radical or a C6 to C20 aryl radical, the concentration of the ionomer in the range 1% to 20% by weight, and the impregnating is carried out at a temperature in the range of from room temperature to 120° C. until the membrane comprises pores substantially filled by the solution; b) subjecting the impregnated membrane to thermal treatment at temperatures from 50° C. to 200° C., until the solvent is substantially removed and the membrane is substantially transparent; c) optionally repeating until the membrane appears substantially transparent; d) treating the membrane with inorganic strong aqueous alkali to convert the functional groups into hydrophilic groups; e) treating the membrane with inorganic strong acids, to convert the (per)fluorinated ionomer to acid hydrophilic form; f) optionally treating with water at a temperature in the range of 50° C. to 100° C. to remove the excess ionomer. 22. The process according to claim 21, wherein the organic solvent has a boiling point at room pressure lower than 180° C.23. The process according to claim 21, wherein the alkali is a hydroxide of Group Ia metals.24. The process according to claim 21, wherein the treating with water is carried out until the water has neutral pH.25. The process according to claim 21, wherein the ionomer is crosslinked by adding cross-linking agents to the (per)fluorinated ionomer solution.26. The process according to claim 25, wherein the cross-linking agents are peroxides, and wherein the temperature of a cross-linking reaction is from 100° C. to 300° C.27. The method of claim 19, wherein the method of separation is microfiltration or ultrafiltration of aqueous solutions.