AU736217B2 - Melt-spun polysulfone semipermeable membranes and methods for making the same - Google Patents

Description

VT

WO 98/29478 PCT/US97/24087 MELT-SPUN POLYSULFONE SEMIPERMEABLE MEMBRANES AND METHODS FOR MAKING THE SAME FIELD OF THE INVENTION The present invention concerns polysulfone semipermeable membranes and methods for making the same. More particularly, the invention pertains to melt-spun polysulfone semipermeable membranes.

BACKGROUND OF THE INVENTION Contemporary semipermeable membranes are available in a variety of forms such as sheets, tubes, and hollow fibers. A "hollow fiber" is generally a hollow cylindrical structure in which the wall functions as a permeable, non-permeable, or semipermeable selectively permeable) membrane depending upon the application. Generally, hollow fibers are used as cylindrical membranes that permit selective exchange of materials across the walls.

Liquid-separation processes utilizing membranes having selective permeabilities, such processes including ultrafiltration, microfiltration, dialysis, reverse osmosis, or the like, require a variety of materials adapted for diversified applications. For example, semipermeable membranes are currently favored for use in extracorporeal blood treatments including hemodialysis, hemofiltration, and hemodiafiltration. In such cases, the membranes typically comprise hollow fibers bundled together and assembled in a casing in a manner allowing blood to flow simultaneously in a parallel manner through the lumina of the fibers while a blood-cleansing liquid is simultaneously passed through the casing so as to bathe the exterior surfaces of the hollow fibers with the liquid.

Compounds utilized for selectively permeable membranes have included polymers, such as cellulose, cellulose acetate, polyamide, polyacrylonitrile, polyvinylalcohol, polymethyl methacrylate, polysulfone, polyolefin, or the like, depending upon the use of the membranes.

Polysulfone compounds are of particular interest as they have, inter alia, excellent physical and chemical properties, such as resistance to heat, resistance to acids, resistance to alkali, and resistance to oxidation. Polysulfone compounds have been found to be biocompatible, capable of forming excellent pores and interstitia, and chemically inert to such compounds as bleach, disinfectants, and salt solutions. Polysulfone compounds can be sterilized by a number of methods, such as ethylene oxide (EtO), gamma irradiation, steam autoclave, and heated citric acid. Additionally, polysulfone compounds possess sufficient strength and resistance to wear to withstand repeated use and sterilization cycles.

Conventionally, polysulfone hollow fibers have been formed by solution-spinning techniques. Producing polysulfone hollow fibers by solution-spinning techniques typically involves dissolving a polysulfone compound in a relatively large amount of an aprotic solvent and a non-solvent, then extruding the solution through a spinneret. For solution spinning, a "solvent" is a compound in which the polysulfone compound substantially dissolves at the membrane- WO 98/29478 PCTIUS97/24087 -2fabrication temperature ambient temperature). For solution spinning, a "non-solvent" is a compound in which the polysulfone compound is substantially insoluble at the membranefabrication temperature. For solution-spinning techniques, the solvents must be sufficient to substantially dissolve the polysulfone compound and produce a homogeneous liquid at ambient temperature (membrane fabrication temperature).

The solvents and non-solvents utilized for solution-spinning techniques require that the membranes be extensively leached and rinsed after fabrication, as even residual amounts left in the membranes can cause unacceptable contamination of fluids treated using the membranes.

Avoiding such contamination is particularly important in membranes used for the treatment of blood by dialysis or the desalination of water by reverse osmosis. When fabricating hollow-fiber membranes utilizing solution spinning techniques, removal of the core liquid used to form the fiber lumen is especially difficult. Following removal of the solvents, non-solvents, and core liquid, a non-volatile, water-soluble compound must then be added to preserve the membrane pore structure prior to drying the membrane. The non-volatile material also serves as a surfactant for later rewetting of the membranes. Such a process is known as "replasticization." Solution-spinning techniques require the inclusion of large amounts of solvents and nonsolvents many of which are generally toxic and can be difficult to extract from the resulting polysulfone fiber. Moreover, the significant amount and high level of toxicity of certain solvents and non-solvents removed from the fibers may create a hazardous waste-disposal problem.

Moreover, conventional solution-spinning techniques produce asymmetric polysulfone membranes non-homogeneous membrane porosity progressing through the thickness dimension of the membrane). That is, a non-homogeneous membrane has a dense skin or microporous barrier layer on one (or both) of the major surfaces of the membrane. The dense skin or micro-porous barrier layer comprises a relatively small portion of the membrane but contributes a disproportionally large amount of control on the permeability characteristics of the membrane.

Accordingly, there is a need for a polysulfone composition and simple method for the production of polysulfone semipermeable membranes which composition and method minimizes toxic waste by-products. Additionally, there is a need for a method for the production of polysulfone semipermeable membranes wherein the solvents, non-solvents, and processing aids used in the manufacture of the membranes are easily removed from the membranes after fabrication and/or are of relatively low toxicity. There is also a need for polysulfone semipermeable membranes having a more uniform structure throughout the thickness dimension a homogeneous polysulfone membrane) so that the entire thickness dimension controls the permeability of the membrane.

SUMMARY OF THE INVENTION In general, the present invention provides, inter alia, a novel method and polysulfone composition for preparing a homogeneous, semipermeable polysulfone membrane by melt-spinning. The polysulfone composition comprises a liquid mixture of a polysulfone C( 1)m LM pond sol vent and. optional a no-o itlthat arc relti vel non1-toXic anld thiat prfe frablv do not dc leterol-SV ailedt thle envirolnent.

ILIS. accordling to one aspect o01 the invencrtio hr spoie etsu J)mVl \'st()InC seipIermecable miembrane. the lysulIfone semlipermeiable mnembrane com1priSMUg a mixture Of'-.

a PI)YNSLII'0ne C01Iompond. and a sol \"ent (as her-einbef'ore defined) 1forI the pol vs II fone com 1)111C iid\verei n sai1d p)O1SLilloneI semlipermecable mnemrbrane has a homogeneC11ous struLcture- suIch t ilic (11 j)I VSuIIl lon sci permleab-le meCIIImran ha s a substantially' Luni 1-1 fomst RuCtlie. and saild poly\sLI'OI one compound and solvent are relatively nion-toxic.

According, to another aspect of' the inventio thrispoie aml-pu j)l0I\LII0C SoC semipermecable memirbrane, defined by a comiposition comlp-ising1: a ixlture_ o1' a poly)SulIIoneC comp)ound.

a sol\'cnt (as hercinibefore defined) for the polysulfoneI comp)ound, and a non-solvent (as hereinbef'ore defined) for1 the polysulf~one Compound, sid p0 )lysuloe semipermeable membrane has a homnogeneous SStruLctur Suc that the pOlySulIIone semipermeable membrane has a substantially uniform structure, and I w \lierein said polysulfone compound, solvent and non-solvent are relatively nion-toxic.

According to a Further aspect of the invention there is provided a mnelt-spun 1)01ysul fone semi permeable membrane, the polysulfonec semipermeable membrane consisting of.

5 a polysulf'one compound, and a solvent (as hereinibefore defined) fior the plYlylfone comp)ound, and the polysuLfIone semnipermeable membrane having a homogeneous structure such that the poI)lyslone semniperm-eable membrane has a substantially uniform structure, wherein said pIolysulIonie compound and solvent are relatively non-toxic.

The solvent may be selected from the group consisting of tetramethylene sulfone ("sul folane"); 3-methyl sulfolane; benzophenone; N,N-dimethylacetamide; 2-pyrrolidone; netylulolene; pyridine; thiophene; o-dichlorobenzene; 1 -chloronaphthalene; methyl salicylate; anisole; o-nitroanisole; diphenyl ether; diphenoxy methane; acetophenone; piiethoxyphenyl-2-ethanol; 2 -piperidine; antipyrine; diethyl phthalate; diphenyl sulfone; A&~diphenyl sulfoxide; plithalic acid, dioctyl ester; phthalic acid, dimethyl ester; phthalic ti :Day LibML B H] 02632.doc: aak ;ICIdl. (liCtihvi ester: hIhIIIalIC acid. d eSter: phljljc aICid. his(-etvll phthIIal ic acid. henz/Vl butylI ester:. and pheIICI Sl~ideC.

I'speccial lv -good reCSults hiavc beeni achied \Vher th o etcmrssSuilolane.C mthl-I Pleni--praoli-D-ort (aniti pvine1). 2-pi1peridi e. 6-vaieroiactam.

dietbl phthiaate- or a m11iXture therelof.

Tie non1-so! vent may be selected From the gron)Ll consistingu of Poly'(ethlNiene cLvkcol di(etlvcnle glyIco tri(efhvienle ,i ycoi). (ulI Ncero I. I .I -d iethlur L1ca: I .3 diet h VIIurea: di I Itr-otoIl nene I 2 -Cthane KII1C- diami e: cii penlam i ne: to! ucnedKaineHI: 0-toIl uIC ac Id: m II-toii a11C iCId: to IueneI- 3.4-di1a m I II: dIL IbVIl )1 hthI alatIe: p~ipei)CdIie: dcc alInI: C\vclohlexanec: cyciohexene1c cill1Orcyciohlexallc: cellosolve" solvenit:

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(lietIl\lbeniviami ne: parafl-in: rmieral oil: minteral wax: tallow, amine: t riethaniol am i ne; lau- rvicthacrviate: stearic acid; ethiylene glycol: tetra(elhyie gi ycoi diethyl adip'e d -sorbi toi: ch loro0triphienly stannanec: resorcinoi 2 -methivI-8-q Inl i no10: li inaidine; 4pheniyl pyridie phiosphorothiic acid. o.o-diethiyl o-(p)-ntrophenryi) ester, NN-dimethyl- 1 p-phenrylenec diamine; 2, 6 -dimethoxypheniol; 4-al lyl- 2 -miclhoxyphenciol; pherimithridl ie; 2aphithylaniiie: i -napihylarnine; I -naphthol; 2 -niaphihaleniethilol; I -bronionaphithalene; leVulinic acid, lihentyl pyrroi-2-y! ketone; pheniyl 4-pyridyl ketone;, isothiocyanic acid, m- 'iitohnietr2-ehlI -idoe 4-mrethiyl imidazole; imidazoic; I ,7-heptaniediol; 9 1-1-lluorenCI-9-o1e; ferrocenie; 2 2 2 "-riitrIlotriethanol; 22 9 -imiriodiethiaroi; dibenizofuran; cvelohexanieacetic acid; cyaniamide; courmarin; 2. 2-bipyridinle; benizoic acid; benizenepropionic, acid; o-dinitrobenzene; 9 -rnethyl-9-azabicyclo(3 I )rionani-3-one; *.ciorodlipheniylarsine; antimony bromide; p-aniisidinie; o-aniisaldlehiyde; adiponitrile; p- :amino acetophienone; monoacetin; diacetin; triacetin; penitoxane; 4-berizoyl biphenyl; meIy o leate; triethyiphosphate; butyrolactonie; terpheny I: tetradecanioi; poliychlori nated bipheniyl ("Aroclor 1242"); myristic acid; methacrylic acid; dodecyl ester; isocyanic acid methylenedi-p-phenyliee ester; Z-R2-hexyloxy)ethoxy] ethianol; 4-niltro biphienyl; benlzyl .tfier: beniezeniesulfonyl chl1oride; 2 4 -diisocyanato-1-1-methyl benzenie; adipic acid, di ethyl ester; 2 '-ritro-acetophenione; I '-acetoniaphithonie; tetradecanone; (dichiloiropleniyl)trichilorosilanie; dichlorodiphienyl silane; phosphorothioic acid, o,o- .0 diethyl o-(p-nitrophenyl) ester; phosphoric acid, tri-o-tolyl ester; phosphoric acid, tripheniyl ester; phosphoric acid, tributyl ester; phenyl phosphorous dichloride; pni tropheniol; isocyanic acid, m-ethyI-m-phenylene ester; 2 2 '-iminodiethano1; N-(2ainioethyl)-N'-2(2-((2aminoethy)amino)ethyl) I 2 -ethanediamine; 2,6-di-tert-butyl pcresol; chioro biphenyl; 4 -biphenylamine; benzyl ether; benzenesulfonyl chloride; 1,2- 3.5 (miethy lenedioxy)-4-propenyl benzene; 2 4 -diisocyanato-I-methyl benzene; chiorodinitro [1A:DayLib\LIBHJ02632.doc~aak 4a benzene (mixed isomers); hexahydro 2H-azepin-2-one; 4,4'-methylenedianiline; 1'acetonaphthone; mercapto acetic acid; and acetanilide. Especially good results have been achieved when the non-solvent comprises poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), glycerol, or a mixture thereof.

The solvent and non-solvent are present in a ratio useful to form a semipermeable, polysulfone membrane useful for performing liquid-separation processes.

In a further aspect the invention relates to a "melt-spinning" or "melt-extrusion" method for producing semipermeable, polysulfone membranes. The melt-spinning method includes the steps of: forming a composition comprising a polysulfone compound, a solvent selected from the foregoing group of candidate solvents and preferably selected from the group consisting of tetramethylene sulfone, antipyrine, 6valerolactam, diethyl phthalate, and mixtures thereof, and, optionally, a non-solvent selected from the foregoing group of candidate non-solvents and preferably selected from the group consisting of poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), 15 glycerol, and mixtures thereof; heating the composition to a temperature at which the composition becomes a homogeneous liquid a temperature greater than ambient); (3) extruding the composition through an extrusion die (such as a single or multi-holed hollow-fibre die (termed a "spinneret"); and passing the extrudate through a quench S. zone in which the extrudate gels and solidifies, thereby forming the membrane.

Thus, according to another aspect of the invention there is provided a melt spinning S process for making a polysulfone semipermeable membrane, the process comprising the steps of: a) forming a composition including a polysulfone compound, a solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore 25 defined) for the polysulfone compound, the solvent and non-solvent being present in the composition in a ratio sufficient to form a semipermeable membrane useful for a liquid separation process; b) heating the composition to a temperature at which the composition is a homogeneous liquid; c) extruding the homogeneous liquid to form an extrudate; and d) thermal quenching the extrudate to cause a phase separation and thereby form a semipermeable membrane; wherein said polysulfone compound, solvent and non-solvent are relatively non-toxic.

[I:\DayLib\LIBH]02632.doc:aak 4b According to yet another aspect of the invention there is provided a melt spinning process for making a polysulfone semipermeable membrane useful for a liquid membrane separation process, the process comprising the steps of: a) forming a composition including a polysulfone compound, a solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore defined) for the polysulfone compound, wherein the solvent and the non-solvent are present in a ratio sufficient to form a semipermeable membrane useful for a liquid separation process; b) heating the composition to a temperature at which the composition is a homogeneous liquid; c) forcing the homogeneous liquid through a strand die to produce solid strands; d) thermal quenching the homogeneous liquid to provide strands; e) pelletising the strands to a particle size readily fed to an extruder.

f) remelting the particles to form a liquid; and 1 5 g) extruding the liquid to form an extrudate and thermal quenching the extrudate to cause a phase separation and form a semipermeable membrane; wherein said polysulfone compound, solvent and non-solvent are relatively non toxic.

*In still another aspect, the present invention relates to melt-spun, semipermeable polysolfone membranes having a uniform structure throughout the thickness dimension of 20 the membrane a "homogeneous" membrane structure) useful for liquid separations, such as, but not limited to, microfiltration, ultrafiltration, reverse osmosis, and dialysis.

Thus, in still a further aspect of the present invention there is provided a melt-spun, substantially homogeneous, semipermeable polysulfone membrane useful for liquid separation processes.

25 Brief Description of the Drawings *ooo Fig. I illustrates a preferred embodiment of the process for fabricating SQ homogeneous polysulfone hollow fibres (as a representative membrane configuration) according to the present invention.

Fig. 2 illustrates an alternative process for fabricating homogeneous polysulfone hollow fibres according to the present invention.

Fig. 3 is a three-component diagram showing the proportions of polysulfone compound, solvent, and non-solvent which are combined in representative melt-spin compositions according to the invention.

[R:\LIBH]02632.doc:aak Fig. 4 is a scanning clectron microscope photograph of a rcpresentative homogeneous, polysul fone hollow fibre according to the present invention.

Fig. 5 is a schematic diagram of a hemodialyzer including homogeneous polysul lone ho! low-fibre membranes oF the present invention.

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[R:\LIBH]02632.doc:aak WO 98/29478 PCT/US97/24087 DETAILED DESCRIPTION This invention encompasses, inter alia, compositions useful for forming, by melt-spinning, polysulfone semipermeable membranes. The compositions comprise a polysulfone compound, a solvent and, optionally, a non-solvent. In the composition, the solvent and optional non-solvent are present in a ratio useful to form a semipermeable membrane useful for performing liquid separation processes. Membranes that are melt-spun using such compositions are homogeneous.

That is, the melt-spun membranes are symmetric such that the membranes have a substantially uniform structure throughout the thickness dimension of the membranes, as illustrated in the scanning electron microscope photograph in Fig. 4 of a hollow fiber made using such a composition. As defined herein, a "homogeneous" polysulfone membrane is a membrane in which each portion or section of the membrane contributes its substantially proportional share to the permeability characteristics of the membrane.

Polysulfone compounds and their synthesis are well-known in the art. Preferred polysulfone compounds useful in this invention satisfy the formula:

RI-SO

2

-R

2 wherein R, and R 2 (which can be the same or different) are groups such as alkanes, alkenes, alkynes, aryls, alkyls, alkoxys, aldehydes, anhydrides, esters, ethers, and mixtures thereof, each such group having fifty or fewer carbon atoms and including both straight-chained and branchedchained structures. Preferred polysulfone compounds useful in this invention have a melt flow index (MFI) in a range of from about 1.7 dg/min to about 9.0 dg/min as measured according to the American Standard Test Method (ASTM) for Flow Rates of Thermoplastics by Extrusion Plastometer, ASTM D 1238-94a. Good results have been achieved when the polysulfone compounds have a MFI of from about 2.0 dg/min to about 5.0 dg/min. Preferred polysulfone compounds useful in this invention include, but are not limited to polyarylsulfones, for example, bisphenol A polysulfone, polyether sulfone, polyphenyl sulfone, and mixtures thereof. Especially good results have been achieved utilizing bisphenol A polysulfone.

A "solvent for the polysulfone compound" is defined herein as a compound having the following characteristics: a boiling point of at least about 150*C, a solvating power to dissolve from about 8 weight percent to about 80 weight percent of the polysulfone compound at a temperature in a range from about 50*C to about 300 0 C. The solvent preferably can dissolve from about 8 weight percent to about 80 weight percent of a polyarylsulfone.

Candidate solvents useful in this invention include, but are not limited to, tetramethylene sulfone; 3-methyl sulfolane; benzophenone; n,n-dimethylacetamide; 2-pyrrolidone; 3methylsulfolene; pyridine; thiophene; o-dichlorobenzene; 1-chloronaphthalene; methyl salicylate; anisole; o-nitroanisole; diphenyl ether; diphenoxy methane; acetophenone; p-methoxyphenyl-2ethanol; 2-piperidine; antipyrine; diethyl phthalate; diphenyl sulfone; diphenyl sulfoxide; phthalic WO 98/29478 PCT/US97/24087 -6acid, dioctyl ester; phithalic acid, dimethyl ester; phithalic acid, diethyl ester; phthalic acid, dibutyl ester; phithalic acid, bis(2-ethylhexyl) ester; plithalic acid, benzyl butyl ester; phenyl sulfide.

Especially preferred solvents useful in this invention include, but are not limited to, tetramethylene sulfone ("sulfolane"), antipyrine, 6-valerolactam, diethyl phithalate, and mixtures thereof. Especially good results have been achieved utilizing tetramethylene sulfone as the solvent.

A 'non-solvent for the polysulfone compound" is defined herein as a compound having the following characteristics: a boiling point of at least about 150 0 C, a solvating power sufficiently low to dissolve less than about 5 weight percent of the polysulfone compound at a temperature in a range from about 50*C to about 300*C.

Candidate non-solvents useful in this invention are 1,1 -diethylurea; 1 ,3-diethylurea; dinitrotoluene; I ,2-ethane diamine; diphenylamine; toluenediamine; o-toluic acid; m-toluic acid; toluene-3,4-diamine; dibutyl phthalate; piperidine; decalin; cyclohexane; cyclohexene; chiorocyclohexane; "cellosolve" solvent; n,n-dimethylbenzylamine; paraffin; mineral oil; mineral wax; tallow amine; triethanol amine; lauryl methacrylate; stearic acid; di(ethylene glycol); tri(ethylene glycol); ethylene glycol; poly(ethylene glycol); tetra(ethylene glycol); glycerin; diethyl adipate; d-sorbitol; chlorotriphenyl stannane; resorcinol; 2-methyl-8-quinolinol; quinaldine; 4phenylpyridine; phosphorothioic acid, o,o-diethyl o-(p-nitrophenyl) ester; N,N-dimethyl-pphenylene diamine; 2,6-dimethoxyphenol; 4-allyl-2-methoxyphenol; phenanthridine; 2naphthylaxmne; l-naphthylamine; 1-naphthol; 2-naphthalenethiol; l-bromonaphthalene; levulinic acid; phenyl pyrrol-2-yl ketone; phenyl 4-pyridyl ketone; isothiocyanic acid, m-nitrophenyl ester; 2-methyl-IH-indole; 4-methyl imidazole; imidazole; I ,7-heptanediol; 9H-fluoren-9-one; ferrocene; 2,2' ,2"-nitrilotriethanol; 2,2 '-iminodiethanol; dibenzofuran; cyclohexaneacetic acid; cyanamide; courmarin; 2,2'-bipyridine; benzoic acid; benzenepropionic acid; o-dinitrobenzene; 9-methyl-9azabicyclo(3.3. l)nonan-3-one; chlorodiphenylarsine; antimony bromide; p-anisidine; oanisaldehyde; adiponitrile; p-amino acetophenone; monoacetin; diacetin; triacetin; pentoxane; 4benzoylbiphenyl; methyl oleate; triethylphosphate; butyrolactone; terphenyl; tetradecanol; polychlorinated biphenyl ('Aroclor 1242"); myristic acid; methacrylic acid, dodecyl ester; isocyanic acid, methylenedi-p-phenylene ester; 2-((2-hexyloxy)ethoxy) ethanol; 4-nitro biphenyl; benzyl ether; benzenesulfonyl chloride; 2,4-diisocyanato-1-l-methyl benzene; adipic acid, diethyl ester; 2'-nitro-acetophenone; 1 -acetonaphthone; tetradecanone; (dichlorophenyl)trichlorosilane; dichiorodiphenyl silane; phosphorothioic acid, o,o-diethyl o-(p-nitrophenyl) ester; phosphoric acid, tri-o-tolyl ester; phosphoric acid, triphenyl ester; phosphoric acid, tributyl ester; phenyl phosphorous dichloride; p-nitrophenol; isocyanic acid, methyl-m-phenylene ester; 2,2'iminodiethanol; N-(2-aminoethyl)-N'-(2-((2-aminoethyl)anmino)ethyl) 1 ,2-ethanediamine; 2,6-ditert-butyl p-cresol; chloro biphenyl; 4-biphenylamine; benzyl eth er; benzenesulfonyl chloride; 1,2- (methylenedioxy)-4-propenyt benzene; 2,4-diisocyanato- 1-methyl benzene; chlorodinitro benzene (mixed isomers); hexahydro 2H-azepin-2-one; 4 4 '-methylenedianiline; I '-acetonaphthone; WO 98/29478 PCT/US97/24087 -7mercapto acetic acid; and acetanilide. Especially preferred non-solvents useful in this invention include, but are not limited to, poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), glycerol, and mixtures thereof.

The concentrations of the components in the composition may vary and are dependent upon variables many of which can be readily worked out with simple bench experiments. For example, miscibility of the composition at the melt-extrusion temperature is one factor to be considered in determining a suitable component concentration. Miscibility of polysulfone compound solutions can be readily determined empirically by methods known in the art.

(Whether or not the components of a composition are miscible is readily apparent.) The end use of the membrane is another factor in determining the appropriate blend composition because the preferred pore size of the membrane and transport rate of liquids and solutes through the membrane vary depending upon the intended fiber end use.

In the case of membranes useful for microfiltration of liquids, the concentration of the polysulfone compound is preferably at least about 8 weight percent, more preferably at least about 12 weight percent. The concentration of the solvent is preferably at least about 40 weight percent, more preferably at least about 60 weight percent. The concentration of the non-solvent, if present, is preferably at least about 1 weight percent, and more preferably at least about weight percent.

In the case of membranes useful for ultrafiltration or dialysis, the concentration of the polysulfone compound is preferably at least about 18 weight percent, more preferably at least about 25 weight percent. The concentration of the solvent is preferably at least about 40 weight percent, more preferably at least about 45 weight percent. Concentration of the non-solvent, if present, is preferably at least about 1 weight percent, more preferably at least about 5 weight percent.

If the non-solvent is present, solvent to non-solvent ratios a solvent to non-solvent ratio "sufficient to form a semipermeable membrane useful for liquid separation processes") are preferably about 0.95:1 to about 80:1, and more preferably about 2:1 to about 10:1. For example, as shown in Fig. 3, for a three-component composition (for melt-spinning polysulfone hollow fibers) comprising bisphenol A polysulfone, sulfolane (the solvent), and poly(ethylene glycol) (the non-solvent), acceptable amounts of the polysulfone compound, solvent, and nonsolvent lie within the area bounded by the extremes of each component which generate the area A, B, C. Any of the specific compositions consisting of an amount of each of the three components within the area A, B, C of Fig. 3 are suitable for melt spinning into hollow-fiber membranes.

In the case of membranes useful for reverse osmosis of liquids, the concentration of polysulfone is preferably at least about 30 weight percent, more preferably at least about weight percent. The concentration of the solvent is preferably at least about 12 weight percent, WO 98/29478 PCT/US97/24087 -8more preferably at least about 20 weight percent. If present, the concentration of the non-solvent is preferably at least about 1 weight percent, more preferably at least about 5 weight percent.

The compositions of this invention may be used to fabricate polysulfone semipermeable membranes useful for "liquid-separation processes." As defined herein, such processes include, but are not limited to, microfiltration, ultrafiltration, dialysis, and reverse osmosis. Fig. 5 shows a representative liquid-separation device configured for use as an extracorporeal blood treatment device, specifically a hemodialyzer. The hemodialyzer 10 comprises an outer casing 12, end caps 14, a dialysate inlet 16, a dialysate outlet 18, a blood inlet 20, a blood outlet 22, and a bundle of fibers 24 potted in the outer casing. The outer casing defines a dialysate compartment, and the lumina of the fibers form a blood compartment. As blood flows through the lumina of the fibers in a parallel fashion, dialysate flows counter-currently through the dialysate compartment.

Membranes of the present invention may be fabricated by alternative method schemes as illustrated in Figs. 1 and 2. A number of method schemes may be followed depending upon the optional method steps chosen to develop the desired polysulfone membrane.

In one preferred method according to the present invention, a polysulfone composition of polysulfone compound, solvent, and optional non-solvent is precompounded in a high-shear mixer, melted, extruded (as hollow fibers), quenched (Fig. and then wound on cores or reels using any number of commercially available winders, such as Leesona winders. In such a method, adequate care should be taken to maintain a slight tension on the hollow fibers during winding. In another preferred method according to the present invention, the polysulfone composition is precompounded in a high-shear mixer, melted, extruded through a strand die (to form solid strands), cooled, pelletized, remelted, extruded (to form hollow fibers), quenched, and then wound (Fig. In still another preferred method according to the present invention, the polysulfone composition is precompounded, melted, extruded (as hollow fibers), quenched, wound, held dry for a period of time, soaked in a liquid that is substantially a non-solvent for the polysulfone compound and stored in the soaking liquid for up to 15 days (Fig. In yet another preferred method according to the present invention, a polysulfone composition is precompounded in a high-shear mixer, melted, extruded (as hollow fibers), quenched, wound, soaked, leached, rinsed, replasticized, and then dried in an oven (preferably a convection oven) (Fig. In another preferred method according to the present invention, the polysulfone composition is precompounded, melted, extruded (as solid strands), cooled, pelletized, remelted, extruded (as hollow fibers), quenched, wound, and then held dry in air followed by soaking in a liquid that is substantially a non-solvent for the polysulfone compound (Fig. In yet another preferred method according to the present invention, a polysulfone composition is precompounded, melted, extruded (as solid strands), cooled, pelletized, remelted, extruded (as hollow fibers), quenched, wound, soaked, leached, rinsed, replasticized, and dried (Fig. 2).

WO 98/29478 PCTIUS97/24087 -9- The components of the composition the polysulfone compound, solvent, and optional non-solvent) to be extruded are combined and homogenized prior to extrusion by mixing in a convenient manner with conventional mixing equipment, as for example, a high-shear mixer, such as a compounding twin-screw extruder. The components of the extrusion composition may also be combined and homogenized directly in a meltpot provided with suitable agitation of the molten liquid. Alternatively, a polysulfone extrusion composition may be homogenized by extruding a molten composition through a strand die, cooling the global extrudate, and grinding or pelletizing the extrudate to a particle size readily-fed to a heated, single-screw or twin-screw extruder.

Alternatively, other heating/homogenizing methods known to those skilled in the art may be utilized to produce a homogeneous, molten liquid for extrusion (termed a "melt").

The melt is heated to a temperature that facilitates preparation of a homogeneous liquid possessing a viscosity suitable for extrusion. The temperature should not be so high as to cause significant degradation of the polysulfone, the solvent, or the non-solvent. The temperature should not be so low as to render the liquid too viscous for extrusion. For example, when the melt comprises bisphenol A polysulfone, the extrusion temperature is preferably at least about more preferably at least about 75'C. The extrusion temperature is preferably less than about 300"C, more preferably less than about 220"C.

The viscosity of the melt should not be so high as to be too viscous to be extruded at temperatures that do not deleteriously affect the polysulfone compound. The viscosity, however, of the melt must not be so low that the extrudate cannot maintain a desired shape upon exiting the extrusion die. The melt may be extruded in a variety of shapes such as, but not limited to, hollow-fibers, tubes, sheets, and hollow-fibers with fins. The extrudate may be aided in retaining its desired shape upon extrusion by cooling.

For making hollow-fiber membranes, the melt is extruded through a hollow-fiber die (spinneret). The spinneret typically is multi-holed and, thus, produces a tow of multiple hollow fibers. The spinneret typically includes a means for supplying a fluid (gas or liquid) to the core or "lumen" of the extrudate. The core fluid is used to prevent collapse of the hollow fibers as they exit the spinneret. The core fluid may be a gas, such as nitrogen, air, carbon dioxide, or other inert gas, or a liquid which is a non-solvent for the polysulfone compound, such as, but not limited to, water, poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), glycerol, and mixtures thereof. Mixtures of solvents and non-solvents may be used as long as the mixture is not a solvent for the polysulfone compound. Alternatively, the melt may first be extruded as solid strands through a single or multi-holed strand die and the resulting solid strands cooled and pelletized to a particle size readily fed to a single-screw or twin-screw extruder (Fig. In this alternative method of production, the particles are remelted and then extruded through a singleholed or multi-holed spinneret to form hollow fibers, as described above.

The extrudate exiting extrusion die enters one or more quench zones. The environment of a quench zone may be gaseous or liquid. Within the quench zone, the extrudate is subjected to WO 98/29478 PCTfUS97/24087 sufficient cooling to cause gelation and solidification of the membrane. In an embodiment of the method of the present invention, the time period beginning after the extrudate exits the die and extending to before the membrane is wound onto a core or reel, is important to attain the desired permeability of the membrane. During this time period, for a given composition, the permeability of the membrane is determined largely by the cooling rate to which the extrudate is subjected. Permeability is increased by rapid quenching of the extrudate, compared to the permeability obtained from a less drastic quench or slower gelling of the extrudate. Increasing permeability of the membranes, which results from more rapid quenching, normally affects the ability of the membranes to transport water, or other liquids and compounds across the thickness dimension of the membranes. Thus, the extrudate cooling rate (as affected by the temperature and composition of the cooling medium employed) may be varied to modify the permeability of the resulting membrane.

In one method according to the present invention, a polysulfone hollow-fiber extrudate is quenched in air. Within the quench zone, the hollow fibers gel and solidify. The temperature of the air-quench zone is preferably less than about 27°C, more preferably less than about 24°C.

The hollow fibers are held in the air zone for preferably less than about 180 minutes, more preferably less than about 30 minutes.

In another preferred method according to the present invention, the hollow-fiber extrudate is quenched in a liquid that is substantially a non-solvent for the polysulfone compound, such as water, poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), glycerol, or a mixture thereof. A mixture of solvent(s) and non-solvent(s) alternatively may be used so long as the mixture remains substantially a non-solvent for the polysulfone compound. When a liquid quench comprises water and one or more other components, the ratio of water to the other components is preferably from about 0.25:1 to about 200:1. The temperature of the liquid quench zone is preferably less than about 50°C, more preferably less than about 25°C, and more preferably less than about 10°C. The advantage of a liquid quench is that it offers less resistance to the transfer of heat from the extrudate to the cooling medium than is present in an air quench and, thus, results in a more rapid removal of heat from the extrudate as the membrane forms. The rapid removal of heat modifies the permeability of the resulting membrane and can be used to tailor membrane permeability for the intended end use.

Hollow fibers are, optionally, drawn using godet rollers or other conventional equipment to the appropriate fiber diameter. More specifically, drawing or stretching the fiber may be accomplished by passing the hollow fiber over a series of rollers. The desired degree of stretching may be obtained by control of the rate of rotation of the second roller or second group of rollers relative to the first roller encountered by the fiber. Line speeds are generally not critical and may vary over a wide range. Preferred line speeds are at least about 10 feet per minute and less than about 1000 feet per minute.

WO 98/29478 PCT/US97/24087 -11- In another preferred method according to the present invention, as illustrated in Fig. 2, following quenching, the membrane is passed through at least one leach bath containing a liquid that is substantially a non-solvent for the polysulfone compound, such as water or a mixture of water and sulfolane and/or the non-solvent(s), or a mixture of water and the solvent utilized in the melt composition. Good results have been achieved when the leach bath is water. The membrane is leached to remove at least a portion of the solvent and the non-solvent. The leach bath need not remove all of the solvent and non-solvent from the membrane, depending, at least in part, on the anticipated end use of the membrane.

The minimum temperature of the leach bath is such that removal of the solvent and nonsolvent from the membrane occurs at a reasonable rate relative to production rate demands. The minimum temperature of the leach bath is preferably at least about 20'C, more preferably at least about 40°C. The maximum temperature of the leach bath is below a temperature at which the integrity of the membrane is deleteriously affected. Accordingly, the temperature of the leach bath is preferably less than about By way of example, the residence time of a hollow-fiber membrane in the leach bath is preferably less than about 1200 seconds, more preferably less than about 300 seconds. The hollow fiber may, optionally, be drawn to the desired size prior to entrance into the leach bath, during the residence time in the leach bath, subsequent to exiting the leach bath, or during any combination thereof.

Following immersion in the leach bath, the membrane may, optionally, be passed through a rinse bath containing water. The rinse bath removes residues in the membrane from the leach process. The rinse bath is preferably maintained at room temperature. For a hollow fiber, the residence time of the fiber within the rinse bath is preferably less than 1200 seconds, more preferably less than 300 seconds.

After leaching, the membrane may then be subjected to a replasticization process. For hollow-fiber membranes to be used for dialysis, a replasticization bath is used that preferably contains less than about 50 weight percent glycerol and more preferably less than about 45 weight percent glycerol, with the balance being water. The minimum temperature of the replasticization bath is such that replasticization of the membrane occurs at reasonable rate relative to production demands. For example, the minimum temperature of a glycerol-containing replasticization bath is preferably at least about 20 0 C, more preferably at least about 35 0 C. The maximum temperature of the replasticization bath is below a temperature at which the membrane integrity could be adversely affected. Accordingly, the maximum temperature of the replasticization bath is preferably less than about 100°C, more preferably less than about 50 0

C.

Following removal of the membrane from the replasticization bath, excess liquid adhering to the membrane may optionally be removed, preferably by use of a conventional air knife operating at a pressure of about 10 psig to about 60 psig. With hollow fibers, good results have been achieved when the air knife is maintained at a pressure of about 30 psig.

WO 98/29478 PCT/US97/24087 -12- The resulting polysulfone membrane may, optionally, be dried in an oven (preferably a convection oven). The oven is maintained at a temperature of from about 20*C to about 200 0

C.

With hollow fibers, good results have been achieved when the temperature of the oven is about 0 C. In a convection oven the membrane is dried for a period of from about 5 seconds to about 1200 seconds. With hollow fibers, good results have been achieved when the fiber was dried for at least about 140 seconds.

The semipermeable polysulfone membranes formed by the described methods may be used in liquid-separation processes such as, but not limited to, microfiltration, ultrafiltration, dialysis, and reverse osmosis. The specific fabrication method that is employed, within the scope of methods according to the present invention, is selected so as to tailor the resulting membrane for its anticipated end use. Such adaption is readily achieved by one skilled in the art based upon the teachings herein.

The following various examples are presented to illustrate the invention only and are not intended to limit the scope of the invention or the following claims.

EXAMPLE 1 A composition was prepared comprising about 36 weight percent Udel P1835NT11, a brand of bisphenol A polysulfone (available from Amoco Polymers, Inc. of Alpharetta, Georgia) about 44.3 weight percent anhydrous sulfolane (available from Phillips Chemical Company of Borger, Texas) and about 17.7 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (available from Dow Chemical Company of Midland, Michigan).

The solvent to non-solvent ratio was about 4.5:1. The composition was compounded in a co-rotating twin-screw extruder at about 132°C. The extruded composition was cooled, pelletized using an RCP 2.0 pelletizer (available from Randcastle Extrusion Systems, Inc., of Cedar Grove, New Jersey), and then remelted and extruded through a 30-hole hollow-fiber spinneret at about 149*C using a single-screw extruder. The resulting hollow-fiber extrudate was quenched in air at about 21 C for about 15 seconds, drawn from a first godet (rotating at a surface speed of 172 feet per minute) to a second godet (rotating at a surface speed of 182 feet per minute) to increase the fiber's length by about 5.75 percent, wound on a core, and soaked in a water bath at a temperature of about 25 0 C for about four hours.

Following soaking in water, the hollow fiber was processed by unwinding the fiber from the core at a rate of about 30 ft/min and passing the fiber through a 37 C water bath for about seconds. The fiber was then immersed in a room temperature water-rinse bath for 139 seconds. Following the rinse bath, the fiber was replasticized by immersion for 140 seconds in a aqueous glycerol replasticization bath held at about 37 0 C. After removing the fiber from the aqueous glycerol bath, excess liquid was removed from the fiber using an air knife operating at about 30 psig. The processed hollow fiber was then dried in a convection oven at about 70°C for 155 seconds.

WO 98/29478 PCT/US97/24087 -13- The resulting hollow fiber had an average lumen diameter of 160 pm, and an average wall thickness of 18 pm. The hollow fiber was fabricated into a dialysis test unit containing 150 fibers. The in vitro water flux of the device was 102.5 mL/(hr-mmHg-m 2 and the average Ko for sodium chloride was found to be 1.92 x 10- 2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber. is defined in the following equation: 1 1 1 Kov K, Pm where Kb is the resistance to mass transfer within the fluid present in the lumen of the hollow fiber, and P, is the membrane permeability. It was not possible to determine the membrane permeability, alone using the test apparatus because the flow of solution through an individual fiber could not be made large enough to render Kb negligible.

This hollow-fiber membrane could be fabricated into a suitable device for use as an ultrafiltration cell for the removal of contaminants from water or aqueous solutions.

EXAMPLE 2 A composition was prepared comprising about 36 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 45.7 weight percent anhydrous sulfolane (Phillips Chemical), and about 18.3 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical), yielding a solvent to non-solvent ratio about 2.5:1.

The composition was compounded in a co-rotating, twin-screw extruder at about 173*C. The extruded composition was then pelletized, remelted, and extruded through a 30-hole hollow-fiber spinneret at about 178°C using a single-screw extruder. The resulting hollow-fiber extrudate was quenched in air at about 22°C for 7-8 seconds. The resulting hollow-fiber membrane was wound on a core at about 110 feet per minute, and held dry for about one hour. The hollow fiber was then placed in a water bath maintained at a temperature of about 25 C for a period of about 12- 15 hours.

The hollow fiber was then processed by unwinding from the core at about 30 ft/min and passing the fiber through a 36°C water leach bath for about 40 seconds. The fiber was immersed in a room temperature water-rinse bath for 139 seconds. The fiber was replasticized for 140 seconds in a 37"C bath of about 40 weight percent aqueous glycerol. After removing the fiber from the aqueous glycerol bath, excess liquid was stripped from the fiber using an air knife operating at a pressure of about 30 psig. The processed fiber was then dried in a convection oven at about 70*C for 155 seconds.

The resulting hollow fiber had an average lumen diameter of about 142 pm, and an average wall thickness of about 31 pm. Dialysis test units each containing 150 of the hollow fibers were fabricated. The average in vitro water flux of these devices was 68.0 WO 98/29478 PCT/US97/24087 -14mL/(hr-mmHg-m 2 and the average Ko,, for sodium chloride was about 2.28 x 10 2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber. This hollow-fiber membrane is useful for ultrafiltration, such as for use in an ultrafiltration cell for the removal of contaminants from water or aqueous solutions.

EXAMPLE 3 A composition was prepared comprising about 38 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 44.3 weight percent anhydrous sulfolane (Phillips Chemical), and about 17.7 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical), yielding a solvent to non-solvent ratio of about 4.5:1. The composition was compounded in a co-rotating, twin-screw extruder at about 99*C, and extruded directly through a 30-hole hollow-fiber spinneret. The extrudate was quenched in air at about 26*C for about 6 seconds. The resulting hollow-fiber membrane was wound on a core at about 160 feet per minute, and placed immediately into a water bath for a period of about 12-15 hours.

The hollow fiber was then unwound from the core at about 30 ft/min and passed through a 37°C water leach bath for about 40 seconds. The fiber was then immersed in a roomtemperature water rinse bath for about 140 seconds. The fiber was replasticized for 140 seconds in an aqueous glycerol bath containing about 40 weight percent glycerol, the bath being held at about 38 0 C. After removing the fiber from the aqueous glycerol bath, excess liquid was removed from the fiber by an air knife operating at a pressure of about 30 psig. The fiber was then dried in a convection oven at about 70*C for about 155 seconds.

The resulting hollow-fiber membrane had an average lumen diameter of 237 sm, and an average wall thickness of 35 /im. Dialysis test units each containing 150 of the resulting fibers were fabricated from this fiber. The average in vitro water flux of these devices was 143.5 mL/(hr-mmHg-m 2 and the average Ko, for sodium chloride was found to be 0.88 x 10-2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber. This hollow-fiber membrane can be used in an ultrafiltration cell for the removal of contaminants from water or aqueous solutions.

EXAMPLE 4 A composition was prepared comprising about 38 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 45.7 weight percent anhydrous sulfolane (Phillips Chemical), and about 18.3 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical), yielding a solvent to non-solvent ratio of about 2.5:1. The composition was compounded in a co-rotating twin-screw extruder at about 143°C, and extruded directly through a 30-hole hollow-fiber spinneret. The extrudate was quenched in air at about 25"C for about 0.08 minutes, wound on a core at about 203 feet per minute, and held dry for thirty minutes before being placed in a 25"C water bath for about three days.

WO 98/29478 PCTIUS97/24087 The hollow fiber was then unwound from the core at about thirty feet per minute and passed through a 38 0 C water-leach bath for about thirty seconds. The fiber was immersed in a room temperature water rinse bath for 148 seconds. The fiber was replasticized for 149 seconds in an aqueous glycerol bath containing about 40 weight percent glycerol, the bath being held at about 38°C. After removing the fiber from the aqueous glycerol bath, excess liquid was removed from the fiber using an air knife operating at a pressure of about thirty psig. The processed hollow fiber was dried in a convection oven at about 70°C for 147 seconds.

The resulting hollow-fiber membrane had an average lumen diameter of 192 and an average wall thickness of 29.5 Dialysis test units each containing 150 of the resulting fibers were fabricated. The average in vitro water flux of these devices was 141.2 mL/(hr-mmHg-m 2 and the average for sodium chloride was found to be 1.20 x 10- 2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber. This hollow-fiber membrane is useful in an ultrafiltration cell for the removal of contaminants from water or aqueous solutions.

EXAMPLE A composition was prepared comprising about 34 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 54 weight percent anhydrous sulfolane (Phillips Chemical Company), about 11 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical Company), and about 1 weight percent glycerol (VanWaters Rogers, Inc., Seattle, Washington), yielding a solvent to non-solvent ratio of about 4.5:1. The composition was compounded in a co-rotating twin-screw extruder at about 144 C.

The extrudate was then cooled, pelletized, remelted, and extruded through a 30-hole hollow-fiber spinneret at about 134 0 C using a single-screw extruder. The resulting extrudate was quenched in air at about 20*C for about 0.08 minute, and wound on a core at about 200 feet per minute. The entire wound core was immediately placed in a 25 0 C water bath for a period of about 15-20 hours.

The hollow fiber was then processed by unwinding the fiber from the core at about 30 feet per minute and passing the fiber through a room-temperature water-leach bath for 97 seconds.

The fiber was replasticized for 145 seconds in a bath containing about 40 weight percent aqueous glycerol held at about 38 0 C. After removing the fiber from the aqueous glycerol bath, excess liquid was stripped from the fiber using an air knife operating a pressure of about 30 psig. The processed hollow fiber was dried in a convection oven at about 62 C for 151 seconds.

The resulting hollow-fiber membrane had an average lumen diameter of about 165 'Um, and an average wall thickness of about 18 Test units each containing about 150 of the resulting fibers were fabricated. The average in vitro water flux of these devices was 67.2 mL/(hr-mmHg-m 2 and the average K, for sodium chloride was found to be 2.19 x 10.2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber.

WO 98/29478 PCT/US97/24087 -16- EXAMPLE 6 A composition was prepared comprising about 34 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 54 weight percent anhydrous sulfolane (Phillips Chemical Company), about 6 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical Company) and about 6 weight percent tri(ethylene glycol) (Aldrich Chemical Company, Inc., Milwaukee, Wisconsin), yielding a solvent to nonsolvent ratio of about 4.5:1. The composition was compounded in a co-rotating, twin-screw extruder at about 153°C. The extrudate was then cooled, pelletized, remelted, and extruded through a 30-hole hollow-fiber spinneret at about 137 0 C using a single-screw extruder. The resulting hollow-fiber extrudate was quenched in air at about 20°C for 0.08 minute, and wound on a core at about 200 feet per minute. The entire fiber core was immediately placed in a water bath for a period of 15-20 hours.

The hollow fiber was then processed by unwinding the fiber from the core at about 30 feet per minute and passing the fiber through a room-temperature water-leach bath for 95 seconds.

The fiber was then immersed in a room-temperature water-rinse bath for 134 seconds. The hollow fiber was replasticized for 146 seconds in a bath of about 40 weight percent aqueous glycerol held at about 38*C. After removing the fiber from the aqueous glycerol bath, excess liquid was stripped from the fiber using an air knife operating at a pressure of about 30 psig.

The processed hollow fiber was dried in a convection oven at about 70°C for 150 seconds.

The resulting hollow-fiber membrane had an average lumen diameter of about 180 pm, and an average wall thickness of about 20 pm. Test units each containing about 150 of the resulting fibers were fabricated. The average in vitro water flux of these devices was 60.0 mL/(hr*mmHg-m 2 and the average K, for sodium chloride was found to be 2.17 x 10.2 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber.

EXAMPLE 7 A composition was prepared comprising about 32 weight percent Udel P1835NT11 polysulfone (Amoco Polymers, Inc.), about 53 weight percent anhydrous sulfolane (Phillips Chemical Company), and about 15 weight percent poly(ethylene glycol) having an average molecular weight of about 1000 daltons (Dow Chemical Company), yielding a solvent to nonsolvent ratio of about 2.5:1. The composition was compounded in a co-rotating twin-screw extruder at about 131 C and extruded directly through a 30-hole hollow-fiber spinneret. The extrudate was quenched in water at about 7 0 C for about 6 seconds. The resulting. hollow-fiber membranes were wound on a core at about 244 feet per minute. The entire fiber core was immediately placed in a 25 0 C water bath for a period of about 15-20 hours.

The hollow fibers were then processed by unwinding the fibers from the core at about feet per minute and passing the fibers through a room-temperature water-leach bath for 97 seconds. The fibers were then immersed in a room-temperature water-rinse bath for 135 seconds.

WO 98/29478 PCT/US97/24087 -17- The fibers were replasticized for 146 seconds in a bath of about 40 weight percent aqueous glycerol, the bath being held at about 38°C. After removing the fibers from the aqueous glycerol bath, excess liquid was stripped from the fiber using an air knife operating at a pressure of about psig. The processed fibers were dried in a convection oven at about 45C for about 152 seconds.

The resulting hollow-fiber membranes had an average lumen diameter of about 203 Jm, and an average wall thickness of about 37 jum. Test units each containing about 150 of the resulting fibers were fabricated. The average in vitro water flux of these devices was 9.1 mL/(hrmmHg'm 2 and the average for sodium chloride was found to be 1.76 x 102 centimeters per minute at a solution flow rate through the fiber lumina of about 0.02 milliliters per minute per fiber.

Having illustrated and described the principles of the invention with several preferred embodiments and multiple various examples, it should be apparent to those skilled in the art that the invention can be modified in arrangement and detail without departing from such principles.

We claim all the modifications coming within the spirit and scope of the following claims.

Claims (48)

1. 3. The membrane of claim 1, wherein the polysulfone compound is selected from the group consisting of bisphenol A polysulfone, polyether polysulfone, polyphenyl polysulfone, and mixtures thereof. i 4. The membrane of claim 1, wherein the solvent is selected from the group consisting of tetramethylene sulfone, antipyrine,
2. 6-valerolactam, diethyl phthalate, and *9 *mixtures thereof A melt-spun polysulfone semipermeable membrane, defined by a composition comprising a mixture of a polysulfone compound, a solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore defined) for the polysulfone compound, wherein I.. said polysulfone semipermeable membrane has a homogeneous structure such 25 that the polysulfone semipermeable membrane has a substantially uniform structure, and wherein said polysulfone compound, solvent and non-solvent are relatively non-toxic. 6. The membrane of claim 5, wherein the non-solvent is selected from the group consisting of 1,1-diethylurea; 1,3-diethylurea; dinitrotoluene; 1,2-ethane diamine; diphenylamine; toluenediamine; o-toluic acid; m-toluic acid; toluene-3,4-diamine; dibutyl phthalate; piperidine; decalin; cyclohexane; cyclohexene; chlorocyclohexane; "cellosolve" solvent; N,N-dimethylbenzylamine; paraffin; mineral oil; mineral wax; RA tallow amine; triethanol amine; lauryl methacrylate; stearic acid; di(ethylene glycol); tri(ethylene glycol); ethylene glycol; poly(ethylene glycol); tetra(ethylene glycol); [R:\LIBH]02632.doc:aak 19 glycerin; diethyl adipate; d-sorbitol; chiorotriphenyl stannane; resorcinol; 2-mnethyl-S- qUinolinol; qUinaldine; 4 -phenylpyridine; phosphorothioic acid, o,o-diethyl nitrophenyl) ester; N,N-dimnethyl-p-phenylene diarnine; 2 ,6-dirnethoxyphenol; 4-allyl-2- mnethoxyphenol; phenanthridine; 2-naphthylarnine; I -naphthylarnine; I -naphthol; 2- naphthalenethiol; l-bromnonaphithalene; levulinic acid; phenyl pyrrol-2-yl ketone; phenyl 4-pyridyl ketone; isothiocyanic acid, m--nitrophenyl ester; 2-methyl- 1H-indole; 4-miethyl imnidazole; imnidazole; I ,7-hieptanediol; 9H-fluoren-9-orie; ferrocene; 9 9',9- nun ilotriethanol; 2 ,'-lininodiethanol; dibenzoftiran; cyclohexaneacetic acid; cyananilde; courmnarin; 2,2'-bipyridine; benzoic acid; benzenepropionic acid; o-dinitrobenzene;
3. 9- imethyl-9-azabicyclo(3 .3.1 )nonani-3-onie; chiorodiphenylarsine; antimony bromide; p- anisidine; o-anisaldehyde; adiponitrile; p-amino acetophenone; monoacetin; diacetin; triacetin; pentoxane; 4 -benzoylbiphenyl; mnethyl oleate; triethyiphosphate; butyrolactone; terphenyl; tetradecanol; polychlorinated biphenyl; myristic acid; mnethacrylic acid, dodecyl ester; isocyanic acid, methylenedi-p-phenylene ester; 2 -fj(2-hexyloxy)ethoxy] 1 5 ethanol; 4-nitro biphenyl, benzyl ether; benezenesulfonyl chloride; 2 ,4-diisocyanlato-l-l- methyl benzene; adipic acid, diethyl ester; 2 '-nitro-acetophenone; I -acetonaphthone;! tetradecanone; (dichlorophenyl)trichlorosi lane; dichlorodiphenyl si lane; phosphorothioic acid, o,o-diethyl o-(p-nitrophenyl) ester; phosphoric acid, tri-o-tolyl ester; phosphoric acid, triphenyl ester; phosphoric acid, tributyl ester; phenyl phosphorous dichloride; p- nitrophenol; isocyanic acid, methyl-m-phenylene ester; 2 ,2'-iminodiethanol; N-(2- am 1nhy)-.4-2(-((-amnoetny)amino) ethyl) I ,2-ethanediamine; 2,6-di-tert-butyl p- cresol; chioro biphenyl; 4-biphenylamine; benzyl ether; benzenesulfonyl chloride; 1,2- (methylenedioxy)-4-propenyl benzene; 2 ,4-diisocyanato- 1-methyl benzene; chlorodinitro benzene (mixed isomers); hexahydro 2H-azepin-2-one; 4 4 '-methylenediani line; 1V- acetonaphthone; mercapto acetic acid; acetanilide, glycerol, and mixtures thereof, wherein the solvent and non-solvent are present in the composition in a ratio sufficient to form a semipermneable membrane useful for liquid-separation processes. 7. The membrane of claim 5 having a viscosity, at a temperature in which the composition is a homogeneous mixture, sufficient to allow melt-extrusion of. the composition to form a semipermeable polysulfone membrane. 8. The membrane of claim 5, wherein the polysulfone compound is a polyarylsulfone compound. [R:\LIBH-]02632.doc:aak t 9. The membrane of claim 5, wherein the polysulfone compound is selected from the group consisting of bisphenol A polysulfone, polyether polysulfone, polyphenyl polysulfone, and mixtures thereof. The membrane of claim 8, wherein the polysulfone compound comprises bisphenol A polysulfone.
4. 11. The membrane of claim 5, comprising between about 8 and about 80 percent by weight polysulfone compound.
5. 12. The membrane of claim 5, comprising at least about 25 percent by weight polysulfone compound. 1 0
6. 13. The membrane of claim 5, wherein the solvent is selected from the group consisting of tetramethylene sulfone, 3-methyl sulfolane, benzophenone, N,N- dimethylacetamide, 2 -pyrrolidone, 3 -methylsulfolene, pyridine, thiophene, o- dichlorobenzene, 1-chloronaphthalene, methyl salicylate, anisole, o-nitroanisole, diphenyl ether, diphenoxy methane, acetophenone, p-methoxyphenyl-2-ethanol, 2-piperidine, 15 antipyrine, 6-valerolactam, diethyl phthalate, diphenyl sulfone, diphenyl sulfoxide, phthalic acid, dioctyl ester, phthalic acid, dimethyl ester, phthalic acid, diethyl ester, phthalic acid, dibutyl ester, phthalic acid, bis(2-ethylhexyl) ester, phthalic acid, benzyl butyl ester, phenyl sulfide, and mixtures thereof.
7. 14. The membrane of claim 5, wherein the solvent is selected from the group consisting of tetramethylene sulfone, antipyrine, 6-valerolactam, diethyl phthalate, and mixtures thereof.
8. 15. The membrane of claim 5, wherein the solvent comprises tetramethylene sulfone. S16. The membrane of claim 5, wherein the solvent and non-solvent are present in 25 a ratio of about 2:1 to about 10:1.
9. 17. A melt-spun polysulfone semipermeable membrane, the polysulfone semipermeable membrane consisting of: a polysulfone compound, and a solvent (as hereinbefore defined) for the polysulfone compound, and the polysulfone semipermeable membrane having a homogeneous structure such that the polysulfone semipermeable membrane has a substantially uniform structure, wherein said polysulfone compound and solvent are relatively non-toxic.
10. 18. The membrane of claim 17, wherein the polysulfone compound is a S polyarylsulfone compound. [R:\LIBH]02632.doc:aak 21
11. 19. The membrane of claim 17, wherein the polysulfone compound is selected from the group consisting of bisphenol A polysulfone, polyether polysulfone, polyphenyl polysulfone, and mixtures thereof. The membrane of claim I 7, %wherein the solvent is selected from the group consisting of tetramethylene sulfone, 3-methyl sulfolane, benzophenone, N,N- dimethylacetamide, 2 -pyrrolidone, 3-methylsul folene, pyridine, thiophene, o- dichlorobenzene, I -chloronaphthalene, methyl salicylate, anisole, o-nitroanisole, diphenyl ether, diphenoxy methane, acetophenone, p-methoxyphenyl-2-ethanol, 2 -piperidine, antipyrine, diethyl phthalate, diphenyl sulfone, diphenyl sulfoxide, phthalic acid, dioctyl ester, phthalic acid, dimethyl ester, phthalic acid, diethyl ester, phthalic acid, dibutyl ester, phthalic acid, bis(2-ethylhexyl) ester, phthalic acid, benzyl butyl ester, phenyl sulfide, and mixtures thereof.
12. 21. A melt spinning process for making a polysulfone semipenrmeable membrane, the process comprising the steps of: a) forming a composition including a polysulfone compound, a solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore defined) for the polysulfone compound, the solvent and non-solvent being present in the composition in a ratio sufficient to form a semipermeable membrane useful for a liquid separation process; b) heating the composition to a temperature at which the composition is a homogeneous liquid; c) extruding the homogeneous liquid to form an extrudate; and d) thermal quenching the extrudate to cause a phase separation and thereby form a semipermeable membrane, wherein said polysulfone compound, solvent and non-solvent are relatively non-toxic.
13. 22. The process of claim 21, wherein the solvent is selected from the group consisting of tetramethylene sulfone, 3-methyl sulfolane, benzophenone, N,N- dimethylacetamide, 2-pyrrolidone, 3 -methylsulfolene, pyridine, thiophene, o- dichlorobenzene, 1-chloronaphthalene, methyl salicylate, anisole, 0-nitroanisole, diphenyl ether, diphenoxy methane, acetophenone, p-methoxyphenyl-2-ethanol, 2-piperidine, antipyrine, 8-valerolactam, diethyl phthalate, diphenyl sulfone, diphenyl sulfoxide, phthalic acid, dioctyl ester, phthalic acid, dimethyl ester, phthalic acid, diethyl ester, phthalic acid, dibutyl ester, phthalic acid, bis(2-ethylhexyl) ester, phthalic acid, benzyl butyl ester, phenyl sulfide, and mixtures thereof. (RA\LIBH]02632.doc:aak 22
14. 23. The process of claim 21, wherein polysulfone compound is a polyarylsulfonc compound.
15. 24. The process of claim 21, wherein the polysulfone compound is selected from the group consisting of bisphenol A polysulfone, polyether polysulfone, polyphenyl polysulfone, and mixtures thereof. The process of claim 21, wherein the non-solvent is selected from the group consisting of poly(ethylene glycol), di(ethylene glycol), tri(ethylene glycol), glycerol, and mixtures thereof.
16. 26. The process of claim 21, wherein the step of quenching the extrudate 0t comprises passing the extrudate through a quench zone, the quench zone comprising a fluid selected from the group consisting of air, water, glycerol, tetramethylene sulfone, and mixtures thereof.
17. 27. The process of claim 21, further comprising the step of drawing the semipermeable membrane. i5 28. The process of claim 21, further comprising the step of storing the semipermeable membrane in a liquid for a period of about 4 hours to about 15 days.
18. 29. The process of claim 28, further comprising the step of passing the semipermeable membrane through a leach bath.
19. 30. The process of claim 28, wherein the leach bath comprises a non-solvent for the polysulfone compound.
20. 31. The process of claim 28, wherein the leach bath comprises water.
21. 32. The process of claim 29, further comprising the step of passing the semipermeable membrane through a rinse bath.
22. 33. The process of claim 32, wherein the rinse bath comprises water. 25 34. The process of claim 32, further comprising the step of passing the semipermeable membrane through a replasticisation bath. The process of claim 34, wherein the replasticisation bath comprises an aqueous glycerol solution.
23. 36. The process of claim 35, wherein the aqueous glycerol solution comprises less than about 50 percent glycerol by weight.
24. 37. The process of claim 34, further comprising the step of drying the semipermeable membrane.
25. 38. The process of claim 37, wherein the semipermeable membrane is dried in an [R:\LIBH]02632.doc:aak
26. 39. A inelt spinning process for making a polysulfone semipermneable membran usefiul for a liquid membrane separation process, the process comprising the steps of: a) forming a composition including a polysulfone compound, a solvent (as hereinbefore defined) for the polysulfone compound, and a non-solvent (as hereinbefore defined) for the polysulfone compound, wherein the solvent and the non-solvent are present in a ratio sufficient to form a semipermeable membrane useful for a liquid separation process; b) heating the composition to a temperature at which the composition is a homogeneous liquid; c) forcing the homogeneous liquid through a strand die to produce solid strands; d) thermal quenching the homogeneous liquid to provide strands; e) pelletising the strands to a particle size readily fed to an extruder. f) remelting the particles to form a liquid; and S Is g) extruding the liquid to form an extrudate and thernal quenching the extrudate to cause a phase separation and form a semipermeable membrane, wherein said polysulfone compound, solvent and non-solvent are relatively non toxic.
27. 40. The process of claim 39 wherein the solvent is selected from the group S.consisting of tetramethylene sulfone, 3-methyl sulfolane, benzophenone, N,N- dimethylacetamide, 2 -pyrrolidone, 3-methylsulfolene, pyridine, thiophene, o- dichlorobenzene, I -chloronaphthalene, methyl salicylate, anisole, o-nitroanisole, diphenyl ether, diphenoxy methane, acetophenone, p-methoxyphenyl-2-ethanol, 2-piperidine, antipyrine, diethyl phthalate, diphenyl sulfone, diphenyl sulfoxide, phthalic acid, dioctyl ester, phthalic acid, dimethyl ester, phthalic acid, diethyl ester, phthalic acid, dibutyl ester, 25 phthalic acid, bis(2-ethylhexyl) ester, phthalic acid, benzyl butyl ester, phenyl sulfide, 8-valerolactam, diethyl phthalate, and mixtures thereof.
28. 41. The process of claim 39 wherein the non-solvent is selected from the group consisting of 1,l-diethylurea; 1,3-diethylurea; dinitrotoluene; 1,2-ethane diamine; diphenylamine; toluenediamine; o-toluic acid; m-toluic acid; toluene-3,4-diamine; dibutyl phthalate; piperidine; decalin; cyclohexane; cyclohexene; chlorocyclohexane; "cellosolve" solvent; N,N-dimethylbenzylamine; paraffin; mineral oil; mineral wax; tallow amine; triethanol amine; lauryl methacrylate; stearic acid; di(ethylene glycol); tri(ethylene glycol); ethylene glycol; poly(ethylene glycol); tetra(ethylene glycol); yj)S~iglycerin; diethyl adipate; d-sorbitol; chlorotriphenyl stannane; resorcinol; 2-methyl-8- [R:\LIBH]02632.doc:aak 24 qulinol;1111 (Llinald]Ine;* 4-plhenylpyridinle; phosphor-othlij acid, o,o-diethyl o-(p-nitrophenyl) ester; N,N-dimnethyl-p-plienylene diamine; 2,6-dimnethoxypheniol; 4- allyl-2-mnethoxyphenol; phenanthridine; 2-naphtliylanine; I -naplithylan-ine; I -naphthol; 2-naplhthalenethiol; I -brornonaphthalene; levulnic acid; phenyl pyrrol-2-yl ketone; phenyl 4-pyridyl ketone; isothiocyanic acid, mi-nitrophenyl ester; 2-m-ethyl-Iindole; 4-mecthyl iidazole; iidazole; I ,7-heptanediol; 9 1-ni-loren-9-one; ferrocene; 2,21,211- iltri lotriethanol 2 2 '-im-inodiethanol; dibenizofuran; cyclohexaneacetic acid; cyanamide; courmnarin; 2,2'-bipyridine; benizoic acid;, benizenepi-oplonic acid; o-dinitrobenizene; 9 -miethyl-9-azabicyclo(3 I )nonan-3-one;- chlorodiphenylarsine; antimony bromide; p-anisidine; o-anisaldehyde; adiponiltri le; p-amnino, acetophenone; rnonoacetin; diacetin triacetin; pentoxane; 4-benizoylbiphenyl; mnethyl oleate; triethyiphosphate; butyrolactone; terphenyl; tetradecanol; p~olychlorinated biphienyl; myristic acid; mnethacrylic acid;, dodecyl ester; isocyanic acid, miethylenedi-p-phenylene ester; 2 2 -hexyloxy)ethoxy] ethanol; 4-nitro biphenyl, benzyl ether; benezenesulfonyl chloride; 2 ,4-diisocyanato-1-l- 1 5 mnethyl benzene; adipic acid, diethyl ester; 2 '-nitro-acetopherione; 1'-acetonaphthone; tetradecanone; (dichlorophenyl)trichlorosi lane; dichlorodiphenyl si lane; phosphorothioic* acid, o,o-diethyl o-(p-nitrophenyl) ester; phosphoric acid, tri-otoyesr;pshri I -tl.etr;p op oi id, triphenyl ester; phosphoric acid, tributyl ester; phenyl phosphorous dichloride; p- nitrophenol; isocyanic acid, methyl-m-phenylene ester; 2,2'-iminodiethanol; N-(2- am inoethyl)-N'-2 (2 -((2am inoethyl)am ino) ethyl) 1 ,2-ethanediamine; 2,6-di-tert-butyl p- cresol; chioro biphenyl, 4-biphenylamine, benzyl ether, benzenesulfonyl chloride, 1,2- (methylenedioxy)-4-propenyl benzene, 2 ,4-diisocyanato- I-methyl benzene, chiorodinitro bezee miedisomers), iiexaiiyuro 2HI-azepin-2-one, ','-methyleneaianiiine, 1- acetonaphthone, mercapto acetic acid, acetanilide, glycerol, and mixtures thereof
29. 42. The process of claim 39, wherein the polysulfone compound is a *..*polyarylsulfone compound.
30. 43. The process of claim 39, further including the step of quenching the extrudate by passing the extrudate through a quench zone, the quench zone comprising a fluid selected from the group consisting of air, water, glycerol, tetramethylene sulfone, and mixtures thereof.
31. 44. The process of claim 39 further comprising the step of drawing the semipermeable membrane. T~ ~45. The process of claim 39, further comprising the step of storing the C-semipermeable membrane in a liquid for a period of about 4 hours to about 15 days. [R:\LIBH]02632.doc:aak
32. 46. The process of claim 39, further comprising the step of passing the semipermeable membrane through a leach bath.
33. 47. The process of claim 46, wherein the leach bith comprises a non-solvent for the polysulfone compound.
34. 48. The process of claim 46, wherein the leach bath comprises water.
35. 49. The process of claim 39, further comprising the step of passing the semipermeable membrane through a rinse bath. The process of claim 49 wherein the rinse bath comprises water.
36. 51. The process of claim 39, further comprising the step of passing the semipermeable membrane through a replasticisation bath.
37. 52. The process of claim 51 wherein the replasticisation bath comprises an aqueous glycerol solution.
38. 53. The process of claim 52 wherein the aqueous glycerol solution comprises less than about 50 percent glycerol by weight. 1 5
39. 54. The process of claim 39, further comprising the step of drying the semipermeable membrane.
40. 55. The process of claim 54, wherein the semipermeable membrane is dried in an 0o oven.
41. 56. A melt-spinning process for making a polysulfone semipermeable membrane, said process being substantially as hereinbefore described with reference to any one of the examples.
42. 57. A process for making a polysulfone semipermeable membrane, said process being substantially as hereinbefore described with reference to figure 1 or figure 2 of the accompanying drawings. 25 58. A semipermeable polysulfone membrane made by the process of any one of claims 21 to 38.
43. 59. A semipermeable polysulfone membrane made by the process any one of claims 39 to 57. A melt-spun, substantially homogeneous, semipermeable polysulfone membrane useful for liquid separation processes.
44. 61. The semipermeable polysulfone membrane of claim 60 having an in vitro water flux value of at least about 9 mL/(hrmmHg-m 2
45. 62. The semipermeable polysulfone membrane of claim 60 comprising a hollow 3 fibre having a lumen and average K for sodium chloride of at least about 0.5 x 10- 2 [R:\LIBH]02632.doc:aak 26 ccintiiinctr-cs per minute at a solution flow rate thr-ough11 the Cibr-e I unien oF01 about 0.02 11ililitreCs perl Minute p~er fi brC.
46. 63. A me1lt-spun11 p)olySl lone semipermneable miembrane, said m-embrane being, suhstantial ly as hereinbefore cscri bed with rcl'i-rence to any one ol the examples.
47. 64. A\ dialyser comprising the semniper-meable. pl)0)sl lone1 membr-ane ofVclaim~ A~n cxtr-acor-porecal blood treatment decvice comiprising the sem ipermeable I vsW I lou mciiibrane of c lai i
48. 66. A lijuii-separation1 (ICViCC comnipiSng tlie scmiper-nicable 1101lSuL1loiiC ncni brac o V cabm p Dated 28 May, 2001 Aithin Medical, Inc. *Patent Attorneys for the Applicant/Nomninated Person SPRUSON FERGUSON V. V.: tR:\LIBH]02632.doc:aak