A method for continuously preparing a formulated polyamide prepolymer, of which the solution viscosity is from 0.25 dL/g to 0.70 dL/g, as measured according to ISO 307:2007 in m-cresol at 20 C., the method including a step of polycondensation on the basis of one or more polyamide precursor monomers, said polycondensation step being carried out in an extruder comprising at least two co-rotating conveying screws, the at least one monomer being previously fed therein in solid or liquid form without being dissolved in a solvent or in water, and said polycondensation step being carried out without extraction of the water formed during said polycondensation step and comprising the addition of at least one additive during said polycondensation step in the extruder.

The present invention provides an organic bioelectronic HD device system for the effective removal of protein-bound substances, comprising PEDOT:PSS, a multiwall carbon nanotube, polyethylene oxide (PEO), and (3-glycidyloxypropyl)trimethoxysilane (GOPS). The composite nanofiber platform exhibited (i) long-term water-resistance; (ii) high adhesion strength on the PES membrane; (iii) enhanced electrical properties; and (iv) good anticoagulant ability and negligible hemolysis of red blood cells, suggesting great suitability for use in developing next-generation bioelectronic medicines for HD.

A method of building viscosity in a sheet molding composition is provided that includes a thickening agent of at least one of magnesium oxide, magnesium hydroxide, calcium oxide, calcium hydroxides, zinc oxide, borates, aluminum ion chelates, aluminum trihydrate, polyphosphate, epoxides being mixed into a phenolic resin liquid or solution that includes novolac resin. An initial viscosity results for the mixture. The viscosity builds from the initial viscosity to 36 hours, from 36 to 142 hours, and then from 142 hours to 176 hours to define a slope ratio of viscosities in these time ranges of 1.5-8:1:-0.4-2 and a having terminal viscosity as measured at 176 hours. Alternatively, the initial viscosity is between 500 and 50,000 centiPoise (cP) and at 24 hours thereafter builds to between 1 million to 50 million cP, and the terminal viscosity thereafter of between 10 million and 200 million cP.

A method of building viscosity in a sheet molding composition is provided that includes a thickening agent of at least one of magnesium oxide, magnesium hydroxide, calcium oxide, calcium hydroxides, zinc oxide, borates, aluminum ion chelates, aluminum trihydrate, polyphosphate, epoxides being mixed into a phenolic resin liquid or solution that includes novolac resin. An initial viscosity results for the mixture. The viscosity builds from the initial viscosity to 36 hours, from 36 to 142 hours, and then from 142 hours to 176 hours to define a slope ratio of viscosities in these time ranges of 1.5-8:1:-0.4-2 and a having terminal viscosity as measured at 176 hours. Alternatively, the initial viscosity is between 500 and 50,000 centiPoise (cP) and at 24 hours thereafter builds to between 1 million to 50 million cP, and the terminal viscosity thereafter of between 10 million and 200 million cP.

An electrolyte membrane is prepared from a liquid composition comprising at least one member selected from the group consisting of trivalent cerium, tetravalent cerium, bivalent manganese and trivalent manganese; and a polymer with a cation-exchange group. The liquid composition is preferably one containing water, a carbonate of cerium or manganese, and a polymer with a cation-exchange group, and a cast film thereof is used as an electrolyte membrane to prepare a membrane-electrode assembly. The present invention successfully provides a membrane-electrode assembly for polymer electrolyte fuel cells being capable of generating the electric power in high energy efficiency, having high power generation performance regardless of the dew point of the feed gas, and being capable of stably generating the electric power over a long period of time.

The present invention relates to a polymeric composition comprising an impact modifier and a mineral filler and its process of preparation and its use. In particular, the present invention relates to a polymeric composition comprising an impact modifier and a mineral filler and its use for thermoplastic polymers. More particularly the present invention relates to the process of preparation of polymeric composition comprising an impact modifier and a mineral filler and its use for the impact modification of thermoplastic polymers.

A process for the manufacture of polycarbonate particles is disclosed herein. The process includes combining a first solution including a polycarbonate and a phosphorus-containing flame retardant or a flame retardant polycarbonate, and an organic solvent with a second solution including a surfactant and an aqueous solvent substantially immiscible with the organic solvent, under conditions of shear and temperature effective to provide an emulsion. At least a portion of the organic solvent is removed from the emulsion to provide an aqueous slurry having a plurality of particles, wherein the particles include the polycarbonate and the phosphorus-containing flame retardant or the flame retardant polycarbonate.

Disclosed is polymer-ceramic composite material with colossal permittivity, comprising polymer matrix and ceramic powders embedded in the polymer matrix, wherein a part of the polymer matrix is exposed and adsorbed to the surface of the ceramic powders, and the polymer is electrically insulating. This invention simultaneously achieves large dielectric constant, negligible dielectric loss and high energy density in flexible composite capacitors based on metal-ion co-doped colossal permittivity materials. The host oxides used in this CP system is friendly to the environment, non-toxic and abundant. Additionally, the process developed is relatively simple, low cost and suitable for mass production-scale. Therefore, these composite capacitors have great technological potential for many applications. Compared to the conventional ceramic materials, composites of this invention are lightweight, scalable and easily fabricated into complex shapes towards miniaturization of the compact systems. The additional flexibility feature also possesses broad application prospects in modern electronic and energy storage devices.

Polymer matrix composite comprising a porous polymeric network; and a plurality of intumescent particles distributed within the polymeric network structure; wherein the intumescent particles are present in a range from 15 to 99 weight percent, based on the total weight of the intumescent particles and the polymer (excluding the solvent); and wherein the polymer matrix composite volumetrically expands at least 2 times its initial volume when exposed to at least one temperature greater than 135 C.; and methods for making the same. The polymer matrix composites are useful, for example, as fillers, thermally initiated fuses, and fire stop devices.

A thermoplastic vulcanizate comprises an isotactic polypropylene matrix phase in which cross-linked rubber particles are dispersed, the rubber particles comprising an ethylene-propylene-diene terpolymer (EPDM) containing at least 40 wt % of ethylene-derived units. A propylene-ethylene-diene terpolymer (PEDM) containing at least 60 wt % propylene-derived units and less than or equal to 25 wt % of ethylene-derived units and having a heat of fusion (H.sub.f) of 2 to 10 J/g is added to compatibilize the propylene/EPDM blend.