Polymer and a membrane having an improved gas-permeability and selectivity

Abstract

A permselective membrane having an improved gas-permeability and selectivity is obtained from a polymer of 1-alkyldimethylsilyl-1-propyne.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a film-forming polymer. More particularly, it relates to a polymer useful for a permselective membrane.

2. Description of the Prior Art

As the materials for producing permselective membranes, there have been known heretofore, several polymers for example, polydimethylsiloxanes and copolymers thereof with polycarbonates or others (U.S. Pat. Nos. 3,980,456, and 3,874,986; and Japan Patent Lay-open No. 26504/1981); as well as olefine polymers such as poly 4-methylpentene-1 (Japan Patent Lay-open No. 4203/1982). However, these polymers can not fulfill all the fundamental requirements, for use as permselective membranes, namely good permeability and selectivity as well as processability to form thin film.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide a polymer capable of forming a membrane having an improved gas-permeability.

It is another object of this invention to provide a polymer formable a membrane having an improved selectivity.

It is still another object of this invention to provide a polymer which can be readily processed into a thin membrane.

It is yet another object of the invention to provide a permselective membrane article, for separating or enriching a specific gas from a gas mixture, having high gaseous permeability and other properties.

Briefly, these and other objects of the present invention as hereinafter will become more readily apparent have been attained broadly by a polymer having repeating units of the formula: ##STR1## wherein R is an alkyl radical having 1-4 carbon atoms.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 is NMR charts of a poly-1-trimethylsilyl propyne,

FIG. 2 and FIG. 3 are IR charts of a poly-1-trimethylsilyl propyne and a poly-1-n-propyldimethylsilyl propyne, respectively.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

In the formula (1), R is an alkyl radical, which may be straight-chain or branched. Examples of suitable alkyl radicals include methyl, ethyl, n- and i-propyl, and n-, i- and t-butyl radicals.

The polymer having the repeating units of the formula (1) can be formed by polymerization of one or more 1-monoalkyl (C1-4) dimethylsilyl-propynes. Suitable monomers include, for example, 1-trimethylsilyl-propyne (sold by Petrarch System Inc. and Chisso Corp., T-3278), and 1-mono-n-propyldimethylsilyl propyne. The most preferred is 1-trimethylsilyl propyne.

Polymerization can be performed under a catalysis of one or more compounds, including halides, of transition metals of group V of Periodic Table, such as niobium and tantalum. Examples of suitable catalysts include NbCl.sub.5, TaCl.sub.5, NbBr.sub.5 and TaBr.sub.5. The most preferred are TaCl.sub.5 and TaBr.sub.5. The catalyst is usually used in an amount of 0.01-20 mol %, preferably 0.5-5 mol %, based on the monomer.

Polymerization may be carried out in the presence of a solvent. Suitable solvents are, for instance, hydrocarbons, including aromatic hydrocarbons, such as benzene, toluene, o-, m- and p-xylenes, ethyl benzene, styrene and naphthalene, cycloaliphatic hydrocarbons, such as cyclohexane, methyl cyclohexane, ethyl cyclohexane and cyclohexene, aliphatic hydrocarbons, such as n-pentane, n- and i-hexanes, n-heptane, n- and i-octanes, 1-hexane, 1-heptene, petroleum ether, and the like; and halogenated hydrocarbons, such as 1,2-dichloroethane, carbon tetrachloride, chloroform, 1,2,3-trichloropropane, trichloroethylene, chlorobenzene, chloroethylbenzene, and the like; as well as mixtures of two or more of these solvents. Among these, preferred are toluene, cyclohexane, n-hexane, and 1,2-dichloroethane. The solvent is generally used in an amount providing a monomer concentration of 0.1-5 mole/l, preferably 1-2 mole/l.

Polymerization can be conducted usually at a temperature of 30.degree. C.-100.degree. C., preferably 50.degree. C.-100.degree. C., more preferably 70.degree. C.-90.degree. C., for 12-36 hours.

The polymerized product may be purified by any known method, for example, by adding the polymer solution into a larger amount of a poor solvent (such as methanol) to precipitate the polymer, followed by filtrating and drying.

Alkyldimethylsilyl propane polymers thus obtained are white solids in fibrous or powdered form.

Weight-average molecular weight of the polymers, determined by light scattering method, is usually at least 10,000 preferably at least 100,000. Polymers obtained by using TaCl.sub.5 or TaBr.sub.5 as the catalyst have higher molecular weight, such as 100,000-2,000,000 or higher. Intrinsic viscosity is generally at least 0.5 dl/g, preferably 1.0-10.0 or more.

Polymers according to the present invention are film-forming, and soluble in various organic solvents as described above (solvents for polymerization) and bellow (solvents for forming membranes); and are particularly useful for producing permselective membranes.

In producing the membrane the polymer according to this invention is dissolved in one or more solvents to form a polymer solution, which is casted to form a film.

Exemplary of suitable solvents are hydrocarbons, for instance, aromatic hydrocarbons, such as benzene, toluene and xylene, cycloaliphatic hydrocarbons, such as cyclohexane, and aliphatic hydrocarbons, such as n-hexane and petroleum ethers; and halogenated hydrocarbons, such as carbon tetrachloride, trichloroethane, trichloroethylene, and the like.

Amoung these, preferred are aliphatic hydrocarbons (b.p.: generally 30.degree.-99.degree. C. preferably 35.degree.-70.degree. C.; particularly n-hexane and petroleum ethers) and mixtures thereof with minor amount (usually 0-50%, preferably 0-30% based on the weight of the total solvent) of other solvents (aromatic hydrocarbons, cycloaliphatic hydrocarbons, halogenated hydrocarbons, or mixtures of two or more of them).

Production of membranes from polymer solutions may be done according to any known methods, such as those described in Japan Patent Lay-open No. 166903/1981, for instance, by casting a polymer solution onto a smooth plain surface of solid (such as metal, glass and the like) or liquid (such as water) followed by evaporating the solvent. Preferred are methods by dropping a dilute polymer solution on a liquid surface (particularly water surface) and then spreading spontaneously on the surface followed by evaporating the solvent to form a ultra thin membrane, which methods can provide membranes free from any serious defeats (such as pin holes) and having a large area.

Besides, molding or forming techniques (such as extrusion technique), generally employed for thermoplastics, may also be applied to obtain membranes.

Membranes composed of one or more alkyldimethylsilyl propyne polymers according to this invention may optionally contain, as mixture or as composite, one or more other polymers.

Examples of suitable polymers include:

(i) Polyorganosiloxanes, such as polydimethylsiloxanes, polymethylphenylsiloxanes, polydiphenylsiloxanes, and derivatives of them (such as polydimethylaminoalkyl (C2-5) methylsiloxanes); and

(ii) olefinic polymers, for example, polymers (including copolymers) of .alpha.-olefines having 2-15 carbon atoms, such as 4-methylpentene-1.

Other examples of suitable polymers are:

(iii) cellulosic materials, including cellulose and derivatives thereof such as cellulose ethers (ethyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, and the like), and cellulose esters (cellulose acetates, such as triacetate, cellulose acetate butyrate, and the like);

(iv) polyalkylsulfones such as copolymers of .alpha.-olefines and SO.sub.2, preferably polymers of long chain alkyl (C10-20) sulfones; and

(v) nitrogen atom-containing polymers, including polymers of tertiary amine-containing vinylmonomers, such as vinylpyridines, N,N-diethylaminoethylacrylate, N,N-dimethylaminostyrene, and the like.

(vi) 1-alkyne polymers, such as those having repeating units of the formula: ##STR2## wherein R.sub.1 is an alkyl radical, particularly branched alkyl radical, having 4-10 carbon atoms, for instance, polymers of t-butyl acetylene, 4-methyl-1-pentyne, 3-methyl-1-pentyne, neopentyl acetylene, t-pentyl acetylene, t-hexyl acetylene, and 1-hexyne; and

(vii) polyvinylorganosilanes, such as those having repeating units of the formula: ##STR3## wherein R.sub.2 is H, C1-12 alkyl, cycloalkyl or aryl radical, and R.sub.3 and R.sub.4, which may be the same or different, are C1-12 alkyl, cycloalkyl or aryl radicals, for example, polymers of vinyltrimethylsilane, vinyltriethylsilane, vinyltripropylsilane, vinyltributylsilane, vinyldimethylethylsilane, vinyltricyclohexylsilane, vinyldimethylcyclohexylsilane, and vinyldimethylphenylsilane.

Among these polymers, preferred are poly-1-alkynes, polyvinylorganosilanes such as polyvinyltrimethylsilanes, polyalkyl (c10--20) sulfones, poly-olefines and alkylcellulose.

Membranes, composed of at least one alkyldimethylsilyl propyne polymer (a) and at least one other polymer (b), may be produced by mixing these polymers (a) and (b) usually in the form of solutions followed by processing to a membrane; or by processing one of the polymers [for instance, the polymer (a)] to a membrane, onto which thereafter the other polymer [the polymer (b)] is coated to form a multi-layer composite membrane; or by combination of these methods.

In membranes composed of said polymers (a) and (b), content of said polymer (a) is usually at least 20%, preferably at least 70% by weight.

Membranes composed of said polymer (a) and optionally the other polymer (b), may contain, if desired, various additives such as plasticizers (esters such as dioctyl phthalate; and higher alcohols or amines having at least 5 carbon atoms, and the like) to improve processability and spreadability of ultrathin membranes.

Membranes according to the invention can take any form of membranes, such as plain filmy, tubular hollow fibrous forms.

Thickness of membranes, which may vary widely, is usually 0.01-100.mu., preferably 0.05-20.mu., in view of practical strength and sufficient permeability.

If necessary, membranes may be supported on one more backing layers to form composites. Suitable materials, used as support, include porous or microporous materials manufactured by various ways, such as extraction, paper-making, phase separation, stretching, and so on. Examples of suitable supports are papers, including Japanese paper, filter paper, synthetic paper, and the like; plastic films, including ultrafiltration membrane and filtration membrane, for example, porous polypropylene film, such as Duragard (brand Name, Celanease Corp.); fabrics, including textile materials such as woven fabrics, knits and non-woven fabrics; and porous glass. Among these preferred are porous polypropylene films such as Duragard and other ultrafiltration membranes.

Thickness of the support is not particularly critical, but is preferably 1.mu.-5 mm, more preferably 10.mu.-1 mm.

Composite membranes can be produced by any known methods. For instance, a thin film formed on water surface is taken out and pressed on a support, or a thin film on water surface is dipped up with a support or sucked through a support to form a composite. If necessary, adhesive may be applied, preferably in scattered way, between the membrane and the support to adhere them. Composite membranes may undertake further heat treatment.

Permselective membranes according to the present invention exhibit an improved oxygen permeability constant, which may range generally 10.sup.-9 -10.sup.-6 cc.multidot.cm/cm.sup.2 .multidot.sec.multidot.mmHg, preferably 10.sup.-8 -10.sup.-6 cc.multidot.cm/cm.sup.2 .multidot.sec.multidot.cmHg; and also enough oxygen/nitrogen separation factor, which may range 1.5-5.

Membranes of this invention have excellent selectivity comparable to those composed of polydimethylsiloxanes, as well as remarkably improved oxygen permeability, say about ten times as high as that of polydimethylsiloxanes.

In addition, alkyldimethylsilyl propyne polymers according to this invention can be readily processed into thin membranes, and their processability is comparable to that of poly-.alpha.-olefines.

Permselective membranes of this invention, having such outstanding virtues as above, yield great advantages for oxygen-enrichment from air, and can be applied to various oxygen-enriching devices, such as engines, boilers, stoves, and other combustors, so as to improve combustion efficiency. Saving of energy of 30-50 percent would be expected by applying to combustion systems membranes according to this invention. Membranes according to the invention can be applicable, for instance, to oxygen-enriching combustion system as described in "NIKKEI PLASTICS", October, 1981, Page 8.

Furthermore, membranes of this invention may be useful for breathing systems, such as incubators for premature or immature babys, curers for respiratory diseases, artificial lungs and artificial gills, as well as contact lens.

Having generally described the invention, a more complete understanding can be obtained by reference to certain specific examples, which are included for purposes of illustration only and are not intended to be limiting unless otherwise specified.

EXAMPLE 1

Polymerization of 1-trimethylsilyl propyne (produced by Petrarch System Inc., T3728) was carried out using TaCl.sub.5 as the catalyst and toluene as the solvent, under the following conditions:

Monomer concentration: 1.0M Catalyst concentration: 20 mM Polymerization temperature: 80.degree. C. Polymerization time: 24 hours

The resulting viscous polymer gel was diluted with toluene to a concentration of 1% by weight. Then the dilute solution was added into a larger amount of methanol to precipitate the polymer, which was then filtered off followed by drying.

The 1-trimethylsilyl propyne polymer thus obtained was identified by analysis of NMR (nuclear magnetic resonance) spectra and IR (infrared) spectrum, which were as shown in FIGS. 1 and 2, respectively; as well as by analysis of UV (ultraviolet) spectrum and elemental analysis, results of which were as follows:

UV Spectral Data (in 5 mM cyclohexene solution): .lambda.max: 273 nm; .epsilon.max: 120 cm.sup.-1 .multidot.(mol/l).sup.-1.

Elemental analysis: C, 64.1%; H, 10.98; Si, 24.92%.

EXAMPLES 2-6

Example 1 was repeated except using the catalyst and the solvent written in Table 1.

Polymers obtained in Examples 1-6 have intrinsic viscosity [.eta.] measured in toluene at 30.degree. C., and weight-average molecular weight (Mw) determined by light scattering method, as shown in Table 1.

TABLE 1______________________________________ Yield, [.eta.], --Mw,Example Solvent Catalyst % dl/g .times. 10.sup.4______________________________________1 Toluene TaCl.sub.5 100 5.5 872 Toluene TaBr.sub.2 90 3.8 623 Cyclohexane TaCl.sub.5 100 6.0 934 Toluene NbCl.sub.5 100 0.99 325 Toluene NbBr.sub.5 100 0.63 276 1,2-Dichloro- TaCl.sub.5 100 2.2 40 ethane______________________________________

EXAMPLES 7 AND 8

Example 1 was repeated except that, instead of 1-trimethylsilyl propyne, was used the monomer as written in Table 2.

The monomers, used in these Examples, were produced by reacting lithium propyne with ethyl- or propyl-dimethylchlorosilane, which was prepared by reacting ethylene or propylene with dimethylchlorosilane.

Polymers obtained in Examples 7 and 8 have [.eta.] and Mw as shown in Table 2.

TABLE 2______________________________________ Yield, [.eta.], Mw,Example Monomer % dl/g .times. 10.sup.4______________________________________7 Ethyldimethylsilyl propyne 100 3.2 548 n-Propyldimethylsilyl propyne 100 2.8 46______________________________________

Results of elemental analysis of these polymers were as follows:

Polymer of Example 7: C, 66.6%; H, 11.1%; Si, 22.2%. Polymer of Example 8: C, 68.6%; H, 11.4%; Si, 20.2%.

IR spectrum of the polymer of Example 8 were as shown in FIG. 3.

EXAMPLE 7-11

Each polymer of Example 1, 2, 3, 7 and 8 was dissolved again in toluene to a concentration of 2% by weight, followed by casting the solution on a glass plate to form a membrane.

Oxygen, nitrogen and hydrogen permeabilities of these membranes were determined by using a gas permeability tester produced by RIKASEIKI KOGYO, JAPAN.

The results were as shown in Table 3.

TABLE 3______________________________________ P*Example Polymer PO.sub.2 PN.sub.2 PH.sub.2 PO.sub.2 /PN.sub.2______________________________________7 of Example 1 52 26 88 2.08 of Example 2 63 28 101 2.29 of Example 3 57 28 12 2.010 of Example 7 9.0 4.0 17.0 2.311 of Example 8 1.0 0.3 3.2 3.3______________________________________ *Gas-permeability constant, 10.sup.-8 cm.sup.3 (STP) cm/cm.sup.2 .multidot. sec .multidot. cmHg

Claims

1. A polymer capable of forming a permselective membrane having an improved gas-permeability, said polymer having repeating units of the formula: ##STR4## wherein R is an alkyl radical containing 1-4 carbon atoms.

2. The polymer of claim 1, said polymer having a weight average molecular weight of at least 10,000.

3. The polymer of claim 1, which is a polymer of 1-trimethylsilyl-1-propyne.

4. The polymer of claim 1, wherein R is methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl or t-butyl.

5. The polymer of claim 1, wherein R is methyl.

6. The polymer of claim 1, wherein R is ethyl.

7. The polymer of claim 1, wherein R is n-propyl.

8. The polymer of claim 1, wherein R is iso-propyl.

9. The polymer of claim 1, wherein R is n-butyl.

10. The polymer of claim 1, wherein R is iso-butyl.

11. The polymer of claim 1, wherein R is t-butyl.