Process for preparation of improved semipermeable composite membranes

• US 4,388,189 A
• Filed: 12/24/1980
• Issued: 06/14/1983
• Est. Priority Date: 12/28/1979
• Status: Expired due to Term

• Current Assignee: Teijin Limited
• Original Assignee: Teijin Limited
• Inventors: Minematsu, Hiroyoshi, Kawaguchi, Takeyuki, Hara, Shigeyoshi, Hayashi, Yuzuru
• Primary Examiner(s): SPEAR JR, FRANK
• Application Number:
  US06/220,081
• Time in Patent Office: 902 Days
• Field of Search: 210/500.2, 210/490, 210/321.1, 427/244, 427/245, 427/246
• US Class Current: 210/490
• CPC Class Codes: B01D 69/125 In situ manufacturing by polymerisation, polycondensation, cross-linking or chemical reaction
• CPC Class Codes: B01D 71/60 Polyamines

Abstract

In a process for producing a semipermeable composite membrane which comprises forming on a microporous substrate a thin layer of a polymeric material comprising a polyamino polymer containing at least 1 milliequivalent, per gram of the polymer in the dry state, of active amino groups selected from primary amino groups and secondary amino groups, and thereafter interfacially crosslinking a surface portion of said thin layer with a crosslinking agent having at least two functional groups (a) capable of easily reacting with either the primary or secondary amino groups or both in said polymer; the improvement wherein

(1) said polymeric material contains dispersed therein a polyfunctional compound having at least two functional groups (b) substantially incapable of reacting with the primary or secondary amino groups in said polymer at a temperature at which the interfacial crosslinking is carried out, but capable of reacting easily with either the primary or secondary amino groups or both in said polymer at a temperature at least 30° C. higher than said crosslinking temperature, and

(2) the interfacially crosslinked thin layer is heated to a temperature at which said polyfunctional compound reacts with the primary or secondary amino groups or both in said polymer.

Claims

1. In a process for producing a semipermeable composite membrane which comprises forming on a microporous substrate a thin layer of polymeric material comprising a polyamino polymer containing at least 1 milliequivalent, per gram of the polymer in the dry state, of active amino groups selected from primary amino groups and secondary amino groups, and thereafter interfacially crosslinking a surface portion of said thin layer with a crosslinking agent comprising a cyclic compound having at least two functional groups (a) selected from the group consisting of carbonyl halide, sulfonyl halide, isocyanate and acid anhydride groups;

the improvement wherein

(1) said polymeric material contains dispersed therein a polyfunctional aliphatic compound having at least two functional groups (b) which are selected from the group consisting of --CH(OH)CH₂ X₁, --COOA₁, --NHCOOA₂, ##STR86## and active halomethyl groups, in which X₁ and X₂ each represent a halogen atom, A₁ and A₂ each represent a hydrogen atom or an organic radical capable of being split off together with the oxygen atom to which it is bonded, and A₃ represents a trivalent or tetravalent saturated aliphatic groups having 2 to 5 carbon atoms, and are substantially incapable of reacting with the primary or secondary amino groups in said polymer at a temperature at which the interfacial crosslinking is carried out, but capable of reacting easily with either the primary or secondary amino groups or both in said polymer at a temperature at least 30°

C. higher than said crosslinking temperature, and

(2) the interfacially crosslinked thin layer is heated to a temperature at which said polyfunctional compound reacts with the primary or secondary amino groups or both in said polymer.

2. The process of claim 1 wherein said functional groups (b) do not substantially react with either the primary or secondary amino groups of said polymer at a temperature of not more than 20°

C., but react easily with either the primary or secondary amino groups or both in said polymer at a temperature of at least 50°

C. but below the self-gelling temperature of said polymer.

3. The process of claim 1 wherein said functional groups (b) do not substantially react with either the primary or secondary amino groups of said polymer at a temperature of not more than 30°

C., but reacts easily with either the primary or secondary amino groups or both in said polymer at a temperature of at least 70°

C. but below the self-gelling temperature of said polymer.

4. The process of claim 1 wherein the polyfunctional compound is a low-molecular-weight or high-molecular-weight polyfunctional compound which dissolves in a solvent selected from water and water-miscible organic solvents having a boiling point of not more than 140°

C. to an extent of at least 0.1 g/100 ml of the solvent at 20°

C.

5. The process of claim 1 wherein the polyfunctional compound is an organic compound containing 2 to 4 functional groups (b) per molecule and having a molecular weight of 90 to 500.

6. The process of claim 1 wherein the polyfunctional compound is a high-molecular-weight organic compound containing said functional groups (b) in an amount of 2.0 to 15.0 milliequivalents per gram of the compound and having a number average molecular weight of 1,000 to 100,000.

7. The process of claim 6 wherein the high-molecular-weight organic compound is a vinyl polymer.

8. The process of claim 1 wherein the polyfunctional compound is a compound selected from compounds of the following formulae ##STR87## in which formulae Q represents a direct bond, an ether linkage, or an alkyl group having 2 to 20 carbon atoms which may contain an oxygen or halogen atom, q is an integer of from 2 to 6, each of X₂, X₃, X₄, X₅, X₆ and X₇ represents a halogen atom, each of A₅, A₁₀ and A₁₁ represents a hydroxyl group, an aliphatic groups containing 1 to 12 carbon atoms and having a valence of a, b or c which may contain an oxygen or halogen atom, an aromatic group containing 6 to 10 carbon atoms and having a valence of a, b or c, or an alicyclic groups containing 5 or 6 carbon atoms and having a valence of a, b or c, each of A₆, A₇, A₈ and A₁₂ represents an alkyl group having 1 to 4 carbon atoms, an allyl group, a phenyl group or an aralkyl group having 7 to 10 carbon atoms, A₉ represents an alkylene group having 2 to 10 carbon atoms, or an arylene group which may be substituted by a halogen atom or an alkyl group having 1 to 6 carbon atoms, and a, b and c each represent an integer of 2 to 4.

9. The process of claim 1 wherein the polyfunctional compound is a high-molecular-weight compound containing at least 40 mole% of at least one recurring unit selected from the group consisting of ##STR88## in which formulae A₈ represents a halogen atom, A₁₃ represents a hydrogen atom or a methyl group, A₁₄ represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, an allyl group, an aralkyl group having 7 to 10 carbon atoms, or a phenyl group, and d is 1 or 2.

10. The process of claim 1 wherein the polyfunctional compound is ethylene glycol dichlorohydrin, glecerol dichlorohydrin, glycerol trichlorohydrin, sorbitol dichlorohydrin, sorbitol trichlorohydrin, sorbitol tetrachlorohydrin, dimethyl tartrate or diethyl tartrate.

11. The process of claim 1 wherein said thin layer contains 0.05 to 1 equivalent, per equivalent of the active amino groups in said polyamino polymer, of said polyfunctional compound.

12. The process of claim 1 wherein said thin layer contains 0.1 to 0.7 equivalent, per equivalent of the active amino groups in the polyamino polymer, of said polyfunctional compound.

13. The process of claim 1 wherein said functional groups (a) react easily with the primary or secondary amino groups or both in said polymer at a temperature of not more than 30°

C.

14. The process of claim 1 wherein said functional groups (a) react easily with the primary or secondary amino groups or both in said polymer at a temperature of not more than 20°

C.

15. The process of claim 1 wherein said functional groups (a) are carbonyl halide or sulfonyl halide groups.

16. The process of claim 15 wherein said cyclic compound is an aromatic compound.

17. The process of claim 1 wherein said crosslinking agent is selected from the group consisting of isophthaloyl chloride, terephthaloyl chloride, trimesoyl trichloride and 3-chlorolsulfonylisophthaloyl chloride.

18. The process of claim 1 wherein said polyamino polymer contains 5.0 to 23.0 milliequivalents, per gram of the polymer in the dry state, of said active amino groups.

19. The process of claim 1 wherein said polyamino compound has a number average molecular weight of 1,000 to 100,000.

20. The process of claim 1 wherein said polyamino polymer has an intrinsic viscosity, determined at 30°

C. for a 1/10 N aqueous solution of sodium chloride, of 0.1 to 2.0 dl/g.

21. The process of claim 1 wherein said polyamino polymer dissolves in at least one solvent selected from the group consisting of water and water-miscible organic solvents having a boiling point of not more than 140°

C. to an extent of at least 0.2 g/100 mg of the solvent at 20°

C.

22. The process of claim 1 wherein said polyamino polymer is a polyaddition product between a polyepoxy compound and a polyamino compound having at least two active amino groups.

23. The process of claim 1 wherein the polyamino polymer is polyethyleneimine, a polyamine-modified polyepichlorohydrin, or a polyamine-modified poly(2-chloroethyl vinyl ether).

24. The process of claim 1 wherein said polyamino polymer is a polymer containing at least 30 mole% of a recurring unit of the following formula ##STR89## wherein R₁₁ and R₁₂ each represent a hydrogen atom or a methyl group and Z₃ represents a direct bond or --SO₂ --.

25. The process of claim 1 wherein the polyamino polymer is a polymer consisting mainly of two recurring units of the formulae ##STR90## wherein R₁₆ represent an alkyl group having 1 to 4 carbon atoms, or of two recurring units of the formulae ##STR91## wherein R₁₆ is as defined above.

26. The process of claim 1 wherein the polyamino polymer is a polymer which does not gel by itself at a temperature of not more than 60°

C.

27. The process of claim 1 wherein said thin layer contains at least 10% by weight of the polyamino polymer.

28. The process of claim 1 wherein said thin layer is formed by applying a solution containing the polyamino polymer and the polyfunctional compound to the microporous substrate, and if desired, partially evaporating the solvent.

29. The process of claim 1 wherein the interfacial crosslinking is carried out at a temperature of about 5°

C. to about 40°

C.

30. The process of claim 1 wherein the interfacially crosslinked layer is heated to about 50°

C. to about 130°

C.

31. A semipermeable composite membrane produced by any one of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30.

32. The membrane of claim 1 which has a water flux of at least 30 liters/m² ·

hr and a NaCl rejection of at least 90% under standard conditions, the ratio of the permeation velocity of NaCl in the initial stage to that after continuous use for 200 hours being not more than 1.50, and which also has a pressure compaction coefficient expressed by the following equation of not more than 0.03;

##EQU4## wherein (WF)₀ is the water flux of the membrane in the initial stage (after 1 hour), and (WF)₂₀₀ is the water flux of the membrane after 200 hours.