Microporous polymeric composition

US10654985B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10654985-B2
Application numberUS-201615571431-A
CountryUS
Kind codeB2
Filing dateMay 26, 2016
Priority dateMay 26, 2015
Publication dateMay 19, 2020
Grant dateMay 19, 2020

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Abstract

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A microporous polymeric composition including a matrix polymer having a fractional free volume of at least 0.1 and dispersed particles having a hypercrosslinked polymer.

First claim

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The invention claimed is: 1. A microporous polymeric composition comprising 60% to 90% by weight of a matrix polymer selected from at least one of substituted polyacetylenes and polymers of intrinsic microporosity (PIMs) and having a fractional free volume of at least 0.1 and dispersed particles comprising 5% to 25% by weight of the microporous polymeric composition of hypercrosslinked polymer comprising optionally substituted aryl groups (Ar) covalently linked by methylene bridging groups (CH 2 ) providing a link with repeating units —(Ar—CH 2 —Ar—CH 2 )n- wherein n is the number of repeating units. 2. A microporous polymeric composition according to claim 1 , wherein the methylene bridging groups form covalent links between two adjacent aryl groups to form a six membered carbocyclic ring that is attached to the aryl rings. 3. A microporous polymeric composition according to claim 1 , wherein the hypercrosslinked polymer is prepared by polymerization of a substituted aryl monomer comprising at least two chloromethylene groups by Friedel Crafts catalysed polymerisation. 4. A microporous polymeric composition according to claim 1 , wherein the hypercrosslinked polymer is prepared by polymerization of an optionally substituted aryl monomer with an external crosslinker. 5. A microporous polymeric composition according to claim 4 , wherein the hypercrosslinked polymer is formed by Friedel Crafts catalysed polymerisation. 6. A microporous polymeric composition according to claim 1 , wherein the hypercrosslinked polymer is formed by post polymerisation crosslinking of polymers containing aryl monomers selected from optionally substituted vinylbenzyl chloride, vinylbenzyl chloride-co-divinylbenzene copolymers, vinylbenzylchloride copolymers having at least two reactive groups to provide a rigid covalent link between two aryl groups. 7. A microporous polymeric composition according to claim 1 , wherein the hypercrosslinked polymer is formed by post polymerisation crosslinking using an external cross-linker of polymers containing aryl monomers. 8. A microporous polymeric composition according to claim 4 , wherein the optionally substituted aryl groups comprise an aryl selected from the group consisting of carbocyclic aryl selected from the group consisting of benzene, biphenyl, naphthylene, tetrahydronaphthylene, idene, azulene, anthracene and heterocyclic aryl selected from the group consisting of furanyl, thiophenyl, 2Hpyrrolyl, pyrrolinyl, oxazolinyl, thiazolinyl, indolinyl, imidazolidinyl, imidazolinyl, pyrazolyl, pyrazolinyl, isoxazolidinyl, isothiazolinyl, oxadiazolinyl, triazolinyl, thiadiazolinyl, tetrazolinyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazenyl, indolyl, isoindolinyl, benzimidazolyl, benzoxazolyl, quinolinyl and isoquinolinyl and optional substituents are selected from the group consisting of C 1 to C 4 alkyl, C 2 to C 4 alkenyl, halo-C 1 to C 4 alkyl, amino, C 1 to C 4 alkylamino, di-(C 1 to C 4 alkyl)amino and sulfonate. 9. A microporous polymeric composition according to claim 1 , wherein the repeating unit of the link comprises formula I or formula II: wherein n represent the number of repeating units. 10. A microporous polymeric composition according to claim 1 , wherein the hypercrosslinked polymer has a Brunauer-Emmett-Teller (BET) surface area in the range of from 500 m2/g to 2500 m2/g. 11. A microporous polymeric composition according to claim 1 , wherein the weight ratio of matrix polymer to hypercrosslinked polymer is at least 4:1. 12. A microporous polymeric composition according to claim 1 , wherein the matrix polymer is soluble in chlorinated hydrocarbon. 13. A microporous polymeric composition according to claim 1 , wherein the matrix polymer having a free volume of at least 0.1 is selected from substituted polyacetylenes. 14. A microporous polymeric composition according to claim 1 , wherein the matrix polymer is a substituted polyacetylene polymer comprising at least one selected from the group consisting of poly(1-(trimethylsilyl)-1-propyne) (PTMSP), poly(1-(dimethyl-n-propylsilyl)-1-propyne), poly(1-(dimethyl-n-butylsilyl)-1propyne), poly(1-phenyl-1-propyne)poly (diphenylacetylene), poly (t-butylacetylene), poly(1-phenyl-2-p-trimethylsilylphenyl-acetylene), poly(1-phenyl-2-p-hydroxyphenylacetylene), poly(4-methyl-2pentyne) and copolymers of two or more thereof. 15. A microporous polymeric composition according to claim 14 , wherein the substituted polyacetylene polymer is poly-1-(trimethylsilyl)-1propyne. 16. A microporous polymeric composition according to claim 1 , in the form of a membrane. 17. A microporous polymeric composition according to claim 16 , for use in gas separations, liquid separations or separation of solids from liquids. 18. A microporous polymeric composition according to claim 16 , wherein the gas permeability of the membrane is more than 80% after 100 days. 19. A microporous polymeric composition according to claim 16 , wherein the gas permeability of the membrane does not decrease by more than 10% over a period of 50 days. 20. A method of preparing microporous polymeric composition according to claim 1 comprising the steps of: (a) dissolving a matrix polymer in a liquid to form a polymer solution, (b) introducing porous particles of the hypercrosslinked polymer to the polymer solution, and (c) subsequently removing at least a portion of the liquid to thereby form the microporous material. 21. A method of performing size-selective separation of a component in a mixture selected from a mixture of fluids or a mixture of a solid and a fluid, the method comprising the steps of: providing the mixture comprising a fluid component; contacting the mixture with one surface of a membrane comprising a microporous polymeric composition according to claim 1 ; applying a pressure difference across the membrane; and isolating a filtered composition from the opposite surface of the membrane to provide a filtered composition enriched in one component of the mixture. 22. A method for separation of liquids by pervaporation comprising the steps of: (a) providing a membrane having a feed side and a permeate side, the membrane comprising a separating layer of a microporous polymeric composition according to claim 1 ; (b) passing a liquid mixture containing a component to be separated across the feed side; (c) providing a driving force for transmembrane permeation; and (d) withdrawing from the permeate side a mixture comprising a gas or vapour enriched in the component compared with the liquid mixture. 23. A method of separation according to claim 22 wherein the mixture of liquids is an aqueous alcohol mixture and the alcohol is enriched on the permeate side. 24. A microporous polymeric composition comprising a matrix polymer having a fractional free volume of at least 0.1 and dispersed particles comprising hypercrosslinked polymer comprising optionally substituted aryl groups covalently linked by methylene bridging groups (CH 2 ) wherein the hypercrosslinked copolymer is obtained by a friedel crafts catalysed polymerisation of either: (a) a substituted aryl monomer comprising at least two chloromethylene groups; or (b) an optionally substituted aryl monomer with an external cross-linker.

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What does patent US10654985B2 cover?
A microporous polymeric composition including a matrix polymer having a fractional free volume of at least 0.1 and dispersed particles having a hypercrosslinked polymer.
Who is the assignee on this patent?
Commw Scient Ind Res Org
What technology area does this patent fall under?
Primary CPC classification C08J9/28. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 19 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).