초록 ▼

Immersion precipitation of solutions having 15%-30% (w/w) and various molecular weights of the emeraldine base form of polyaniline in polar aprotic solvents are shown to form integrally skinned asymmetric membranes and fibers having skin layers <1 μm thick which exhibit improved rates of gas

Immersion precipitation of solutions having 15%-30% (w/w) and various molecular weights of the emeraldine base form of polyaniline in polar aprotic solvents are shown to form integrally skinned asymmetric membranes and fibers having skin layers <1 μm thick which exhibit improved rates of gas transport while preserving good selectivity. These membranes can be further transformed by an acid doping process after fabrication to achieve excellent permeation rates and high selectivities for particular gas separations. Prior to the use of concentrated EB solutions, the formation of integrally skinned asymmetric membranes was not possible, since films and fibers made from <5% w/w polyaniline solutions were found to disintegrate during the IP process.

대표청구항 ▼

What is claimed is: 1. A method for preparing an integrally skinned, gas permeable asymmetric hollow fiber which comprises the steps of: (a) forming a solution of the emeraldine base (EB) form of polyaniline having between 15% and 30% w/w of polyaniline; (b) adding a gel inhibitor to the solution;

What is claimed is: 1. A method for preparing an integrally skinned, gas permeable asymmetric hollow fiber which comprises the steps of: (a) forming a solution of the emeraldine base (EB) form of polyaniline having between 15% and 30% w/w of polyaniline; (b) adding a gel inhibitor to the solution; (c) extruding the solution through the outer bore of a hollow fiber spinnerrette nozzle; (d) passing the solution through an air-gap; and (e) directing the extruded solution into a coagulation bath containing a nonsolvent for polyaniline, whereby an asymmetric hollow fiber having a permeable dense skin in the vicinity of the surfaces thereof in contact with the nonsolvent and a lower-density porous interior support portion is formed. 2. The method as described in claim 1, wherein the EB form of polyaniline comprises high-molecular weight polyaniline. 3. The method as described in claim 2, wherein the nonsolvent for polyaniline comprises water. 4. The method as described in claim 1, wherein the gel inhibitor is selected from the group consisting of primary, secondary and tertiary amines. 5. The method as described in claim 1, further including the step of drying the hollow fiber after said step of directing the extruded solution into a coagulation bath. 6. The method as described in claim 1, further including the step of caulking the dense skin after said step of directing the extruded solution into a coagulation bath. 7. The method as described in claim 6, wherein the caulking compound comprises silicon elastomer. 8. The method as described in claim 7, wherein the silicon elastomer comprises polydimethylsiloxane. 9. The method as described in claim 1, further comprising the step of heating the hollow fiber for a chosen period in order to improve gas selectivity. 10. The method as described in claim 1, further comprising the step of acid doping the hollow fiber in order to improve gas selectivity. 11. The method as described in claim 1, wherein in addition to the EB form of polyaniline, a polymer other than polyaniline is added to the solution in said step of forming a solution of the EB form of polyaniline, whereby a blended integrally skinned, porous asymmetric hollow fiber is formed. 12. The method as described in claim 11, wherein said polymer comprises polysulfones.