Abstract: The invention relates to polymers comprising sulfonated 2,6-diphenyl-1,4-phenylene oxide repeating units, to a method for their preparation, and to their use in a membrane electrode assembly, in a proton exchange membrane, in a fuel cell, in an electrolyser, in an electrolytic hydrogen compressor or in a flow battery. The invention further relates to a proton exchange membrane comprising said polymer and to a method for the preparation of a proton exchange membrane from said polymer. The invention also relates to the use of the polymers in ion exchange materials.

Abstract: The invention relates to polymers comprising sulfonated 2,6-diphenyl-1,4-phenylene oxide repeating units, to a method for their preparation, and to their use in a membrane electrode assembly, in a proton exchange membrane, in a fuel cell, in an electrolyser, in an electrolytic hydrogen compressor or in a flow battery. The invention further relates to a proton exchange membrane comprising said polymer and to a method for the preparation of a proton exchange membrane from said polymer. The invention also relates to the use of the polymers in ion exchange materials.

Abstract: The present invention relates to process for crosslinking an arylene oxide polymer comprising a 3-pyridyl and/or a 4-pyridyl group, wherein the polymer is reacted with a compound according to Formula (1) or a compound according to Formula (2), wherein R1, R2, R3 and R4 are independently selected from the group consisting of hydrogen, halogen, hydroxy and cyano. The crosslinked arylene oxide polymer can be used as a membrane, in particular a proton conducting membrane.

Abstract: The present invention relates to process for crosslinking an arylene oxide polymer comprising a 3-pyridyl and/or a 4-pyridyl group, wherein the polymer is reacted with a compound according to Formula (1) or a compound according to Formula (2), wherein R1, R2, R3 and R4 are independently selected from the group consisting of hydrogen, halogen, hydroxy and cyano. The crosslinked arylene oxide polymer can be used as a membrane, in particular a proton conducting membrane.

Abstract: The present invention relates to A phenol compound according to Formula (I): wherein: R1 is selected from the group consisting of, optionally substituted, 2-pyridyl, 3-pyridiyl and 4-pyridyl groups, wherein R1 is at position 2 or 3 of the phenol ring; R2 is selected from the group consisting of, optionally substituted, 2-pyridyl, 3-pyridiyl, 4-pyridyl and phenyl groups, wherein R2 is at position 5 or 6 of the phenol ring; and the phenol ring is optionally substituted at one or two positions, independently selected from positions 2, 3, 5 and 6, with a halogen atom or a with an optionally substituted C6-C12 aryl group or an optionally substituted C1-C10 alkyl group. The present invention relates also to (co)polymers comprising the phenol compound according to Formula (I) and membranes and ionic resins comprising said (co)polymers.

Abstract: Disclosed are processes for preparing polyareneazole polymers characterized as providing polymer solutions having an inherent viscosity of at least about 22 dl/g at 30° C. at a polymer concentration of 0.05 g/dl in methane sulfonic acid. Polyareneazoles, filaments and yarns are also disclosed.

Abstract: The present invention relates to the use of a (1?3)-?-D-glucan as an emulsion stabilizer. The present invention further relates to emulsions comprising a (1?3)-?-D-glucan in an amount of 0.01 to 10 wt. %, based on the total weight of the emulsion. The present invention also relates to bitumen binder compositions comprising a (1?3)-?-D-glucan in an amount of 0.005 to less than 0.1 wt. %, based on the total weight of the bitumen binder composition. The present invention further relates to emulsions comprising a novel biodegradable emulsifying agent, in particular in combination with a (1?3)-?-D-glucan.

Abstract: The present invention relates to the use of a (1?3)-?-D-glucan as an emulsion stabiliser. The present invention further relates to emulsions comprising a (1?3)-?-D-glucan in an amount of 0.01 to 10 wt. %, based on the total weight of the emulsion. The present invention also relates to bitumen binder compositions comprising a (1?3)-?-D-glucan in an amount of 0.005 to less than 0.1 wt. %, based on the total weight of the bitumen binder composition. The present invention further relates to emulsions comprising a novel biodegradable emulsifying agent, in particular in combination with a (1?3)-?-D-glucan.

Abstract: The present invention relates to processes for hydrolyzing polyphosphoric acid in a fiber and the removal of hydrolyzed polyphosphoric acid from the fiber.

Abstract: The present invention relates to processes for hydrolyzing polyphosphoric acid in a fiber and the removal of hydrolyzed polyphosphoric acid from the fiber.

Abstract: The present invention relates to processes for removing phosphorus from a fiber or yarn.

Abstract: Disclosed are processes for preparing monomer complexes that include contacting 2,3,5,6-tetraminopyridine free base in water with 2,5-dihydroxy terephthalic acid dipotassium salt to form an aqueous mixture, and adjusting the pH of the aqueous mixture to within the range of from about (3) to about (5) to precipitate the monomer complex. Processes of polymerizing the monomer complexes, polyareneazoles, filaments and yarns are also disclosed.

Abstract: The present invention concerns a process for making a polyareneazole multifilament yarn comprising: a) extruding a solution comprising polyareneazole polymer and polyphosphoric acid through a plurality of orifices to produce filaments; b) forming a multifilament yarn from said filaments; c) hydrolyzing at least some of the polyphosphoric acid in the yarn by heating the yarn to a temperature above about 120° C. for up to about two minutes; d) washing at least some of the hydrolyzed polyphosphoric acid from the yarn; e) drying the washed yarn; f) optionally, heating the yarn above about 300° C., and g) collecting the yarn at a speed of at least about 50 meters per minute.

Abstract: The present invention relates to processes for removing phosphorus from a fiber or yarn.

Abstract: The present invention relates to processes for hydrolyzing polyphosphoric acid in a fiber and the removal of hydrolyzed polyphosphoric acid from the fiber.

Abstract: The present invention relates to processes for removing cations from a polyareneazole fiber.

Abstract: Disclosed are thermal processes for increasing polyareneazole inherent viscosities.

Abstract: Disclosed are processes for preparing polyareneazole polymers including contacting a molar excess of a free base in water with a terephthalic acid salt to form an aqueous mixture, adjusting the pH to precipitate a monomer complex, contacting the monomer complex with metal powder, and polymerizing the monomer complex. Polyareneazoles, filaments and yarns are also disclosed.

Abstract: The present invention concerns a process for making a polyareneazole polymer comprising the steps of: a) contacting azole-forming monomers, metal powder, and optionally P2O5, in polyphosphoric acid to form a mixture; b) blending the mixture at a temperature of from about 50° C. to about 110° C.; c) further blending the mixture at a temperature of up to about 145° C. to form a solution comprising an oligomer; d) optionally, degassing the solution; and e) reacting the oligomer solution at a temperature of about 160° C. to about 250° C. for a time sufficient to form a polymer.

Abstract: Disclosed are processes for preparing polyareneazole polymers that include contacting, in polyphosphoric acid, azole-forming monomers and metal powder, the metal powder added in an amount of from about 0.05 to about 0.9 weight percent, based on the total weight of the azole-forming monomers, and reacting the azole-forming monomers to form the polyareneazole polymers. Polyareneazoles, filaments and yarns are also disclosed.