US2022118409A1PendingUtilityA1
Method of preparting membranes
Est. expiryNov 20, 2035(~9.3 yrs left)· nominal 20-yr term from priority
C08L 81/06C08L 71/02C08L 27/16C08J 2471/02C08J 2381/06C08J 5/18C08G 2650/50B29L 2031/755B29K 2081/06B29K 2027/16B29C 41/30B01D 2323/18B01D 2323/12B01D 71/68B01D 71/34B01D 69/02B01D 67/0088B01D 71/5211B01D 2325/34B01D 67/0011B01D 67/0013B01D 67/0016B01D 71/52B01D 71/60B01D 71/421B01D 71/261B01D 61/025B01D 61/027B01D 2323/219
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Claims
Abstract
A method of preparing a membrane comprising the steps of: a) mixing together a membrane-forming polymer, a water-soluble polyetheramine, and a solvent, said mixture containing no component which will react chemically with the polyetheramine; and b) casting said mixture to form the polymer into a solid membrane.
Claims
exact text as granted — not AI-modified1 - 7 . (canceled)
8 . A method of preparing a membrane comprising the steps of:
a) mixing together a membrane-forming polymer, a water-soluble polyetheramine which is a polyether with at least one primary or secondary amine group attached to the polyether backbone, and a solvent, said mixture containing no component which will react chemically with the polyetheramine; and b) casting said mixture to form the polymer into a solid membrane.
9 . A method as claimed in claim 8 , in which the water solubility of the polyetheramine is at least 0.1% w/v at 21° C.
10 . A method as claimed in claim 9 , in which the water solubility of the polyetheramine is at least 0.2% w/v at 21° C.
11 . A method as claimed in claim 10 , in which the polyetheramine is miscible with water at 21° C.
12 . A method as claimed in claim 8 , in which the polyetheramine has a molecular weight of up to 2,500.
13 . A method as claimed in claim 8 , in which the polyetheramine contains two or more ethylene oxide and/or propylene oxide monomer units and at least one primary or secondary amine unit —NHX where X is a hydrogen atom or a C 1-4 alkyl group.
14 . A method as claimed in claim 8 , in which the polyetheramine is a mono- or di-amine having the schematic formula:
Y—PAO—Y′ (I)
or a mono-, di- or tri-amine having the schematic formula:
in which each of Y, Y′ and Y″ independently represents an end group at least one of which includes a primary or secondary amine group, and PAO represents a polyalkyleneoxide chain consisting of at least two ethylene oxide and/or propylene oxide monomer units.
15 . A method as claimed in claim 14 , in which the polyetheramine has the schematic formula:
Y—(O—CH 2 —CH(CH 3 )) a —(O—CH 2 —CH 2 ) b —Y′ (III)
in which a represents the number of propylene oxide monomer units present and b represents the number of ethylene oxide monomer units present; or the general formula:
in which R represents a hydrogen atom or a methyl group, R′ represents a hydrogen atom, a methyl or an ethyl group, d is 0 or 1, and c, e and f are the number of propylene oxide and/or ethylene oxide monomer units present.
16 . A method as claimed in claim 8 , in which the polyetheramine has one of the formulae:
in which R is H or CH 3 , and x and y are the numbers of propylene oxide and/or ethylene oxide monomer units in the polyether chain;
in which x is the number of propylene oxide monomer units in the polyether chain;
in which x and z are the number of propylene oxide monomer units in two blocks in the polymer chain, and y is the number of EO monomer units in the polyether chain;
in which x is 2 or 3;
in which x, y and z together represent the total number of propylene oxide monomer units present in the branched chain polymer, n is 0 or 1, and R is hydrogen, methyl or ethyl;
or a compound of one of the formulae (V) to (IX) above in which one or more of the NH 2 end groups has been converted into a secondary amine group.
17 . A method as claimed in claim 16 , in which the polyetheramine has the formula (IX), in which the number of moles of polyethylene oxide is between 5 and 6; or in which the polyetheramine has the formula (VI), in which x in the formula (VI) is on average from 6 to 7.
18 . A method as claimed in claim 8 , in which the membrane-forming polymer is selected from cellulose acetate/triacetate; polyamide; polypiperazine; polybenzimidazoline; polysulfone; polyol; polyacrylonitrile; polyethersulfone; polysulfone; poly(phthalazinone ether sulfone ketone; poly(vinyl butyral); polyvinylidene fluoride; poly(tetrafluoroethylene); polypropylene; polyethylene; and polyetheretherketone.
19 . A method as claimed in claim 8 , in which step (b) comprises immersing the mixture produced in step (a) in a medium in which the polymer is insoluble.
20 . A method as claimed in claim 8 , in which the membrane obtained in step (b) is subsequently provided with a coating.
21 . A membrane preparable by the method as claimed in claim 8 .
22 . A membrane as claimed in claim 21 , which is an ultrafiltration membrane, a nanofiltration membrane or a reverse osmosis membrane.
23 . A membrane comprising a water-soluble polyetheramine which is a polyether with at least one primary or secondary amine group attached to the polyether backbone, wherein the membrane contains no component which is chemically reactive with the polyetheramine.
24 . A membrane as claimed in claim 23 , wherein the water solubility of the polyetheramine is at least 0.1% w/v at 21° C.
25 . A membrane as claimed in claim 24 , which is an ultrafiltration membrane, a nanofiltration membrane or a reverse osmosis membrane.
26 . A membrane which has a molecular weight cut off of at least 20 kDa and a flux of at least 20 GFD/psi.
27 . A membrane as claimed in claim 26 , which is an ultrafiltration membrane, a nanofiltration membrane or a reverse osmosis membrane.Cited by (0)
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