Abstract: This disclosure relates to polymeric membranes that incorporate a hydroxyl-functionalized CARDO moiety that can be used in sour natural gas separation and purification applications.

Abstract: A gas separation membrane is provided. The gas separation membrane includes a poly(imide-oxadiazole) polymer including an oligomer having a structure comprising: In this structure, Ar1, Ar2, and Ar3 include aromatic moieties, and wherein Ar1, Ar2, and Ar3 are each independently selected.

Abstract: Embodiments described in examples herein provide a gas separation membrane including a polyimide polymer including a monomer having a structure including: wherein when X1=X2, X1 and X2 are selected from F, Cl, Br, or I and wherein when X1 and X2 are different elements, X1 and X2 are independently selected from H, F, Cl, Br, or I.

Abstract: A membrane system includes a first membrane and a second membrane. At a given temperature and pressure: the first membrane has a permeation rate for a first gas and a selectivity for a gas mixture comprising the first gas a second gas different from the first gas; the second membrane has a permeation rate for the first gas and a selectivity for the gas mixture; the permeation rate of the first membrane is greater than the permeation rate of the second membrane; and the selectivity of the second membrane is greater than the selectivity of the first membrane.

Abstract: Compositions of and methods for producing a modified polyimide-containing compound with an alkyl or acyl group, one method including selecting and preparing a polyimide-containing compound to undergo a Friedel-Crafts alkylation or acylation reaction; carrying out the Friedel-Crafts alkylation or acylation reaction on the polyimide-containing compound to bond an alkyl group or acyl group to a reactive site on an aromatic compound of the polyimide-containing compound; cleaving the polyimide-containing compound to produce modified monomers comprising the alkyl group or the acyl group; and using the modified monomers in a reaction to produce the modified polyimide-containing compound, wherein the alkyl group or the acyl group is present in the modified polyimide-containing compound.

Abstract: A gas separation membrane is provided. The gas separation membrane includes a poly(imide-oxadiazole) polymer including an oligomer having a structure comprising: In this structure, Ar1, Ar2, and Ar3 include aromatic moieties, and wherein Ar1, Ar2, and Ar3 are each independently selected.

Abstract: Compositions of and methods for producing a modified polyimide-containing compound with an alkyl or acyl group, one method including selecting and preparing a polyimide-containing compound to undergo a Friedel-Crafts alkylation or acylation reaction; carrying out the Friedel-Crafts alkylation or acylation reaction on the polyimide-containing compound to bond an alkyl group or acyl group to a reactive site on an aromatic compound of the polyimide-containing compound; cleaving the polyimide-containing compound to produce modified monomers comprising the alkyl group or the acyl group; and using the modified monomers in a reaction to produce the modified polyimide-containing compound, wherein the alkyl group or the acyl group is present in the modified polyimide-containing compound.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: Co-polyimide membranes for separating components of sour natural gas including at least three distinct moieties polymerized together, the moieties including a 2,2?-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a 2,4,6-trimethyl-m-phenylenediamine (DAM) based moiety; and at least one component selected from the group consisting of: a 4,4?-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2?-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3?-dihydroxybenzidine based moiety; and a 3,3?-(hexafluoroisopropylidene)dianiline based moiety.

Abstract: Co-polyimide membranes for separating components of sour natural gas including at least three distinct moieties polymerized together, the moieties including a 2,2?-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a 4,4?-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; and at least one component selected from the group consisting of: a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2?-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3?-dihydroxybenzidine based moiety; and a 3,3?-(hexafluoroisopropylidene)dianiline based moiety.

Abstract: Co-polyimide membranes for separating components of sour natural gas including at least three distinct moieties polymerized together, the moieties including a 2,2?-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a 2,4,6-trimethyl-m-phenylenediamine (DAM) based moiety; and at least one component selected from the group consisting of: a 4,4?-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2?-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3?-dihydroxybenzidine based moiety; and a 3,3?-(hexafluoroisopropylidene)dianiline based moiety.

Abstract: Co-polyimide membranes for separating components of sour natural gas including at least three distinct moieties polymerized together, the moieties including a 2,2?-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a 4,4?-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; and at least one component selected from the group consisting of: a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2?-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3?-dihydroxybenzidine based moiety; and a 3,3?-(hexafluoroisopropylidene)dianiline based moiety.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Abstract: A molecule possessing a primary or secondary amino group and an additional functionality capable of providing a novel or improved property to a cellulose material has been permanently attached to the cellulose material in aqueous media using a water-soluble carbodiimide as the coupling agent/activator. One such molecule is 5-aminofluorescein (abbreviated as “A-fluo”) and one such cellulose material is a papermaking pulp. Papers made from a pulp furnish containing, for example, 0.01 wt. % of the “A-fluo”-attached pulp show an embedded marker feature authenticable upon UV or visible light excitation. The “A-fluo”-attached pulp can also be used for the marking and identification of a pulp furnish.

Abstract: A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH?CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.