A method for preparing an aliphatic polyester resin powder includes the steps of a) heat dissolving a crystalline aliphatic polyester resin in an organic solvent to obtain an aliphatic polyester resin solution; b) cooling the aliphatic polyester resin solution to precipitate a solid, thereby obtaining a solid-liquid mixture; c) optionally adding an adjuvant to the solid-liquid mixture and mixing; and d) conducting solid-liquid separation and drying to obtain an aliphatic polyester resin powder suitable for selective laser sintering. The crystalline aliphatic polyester resin powder obtained has good antioxidant property, good powder flowability, moderate size, smooth surface, suitable bulk density, and suitable dispersibility and particle size distribution. The aliphatic polyester resin powder is particularly suitable for selective laser sintering method.

This invention provides a method for creating a large-scale of amphiphilic particles. The method includes: adding nanoparticles into a polycarbonate-based solution, adding a surfactant into the solution while performing ultra-sonication to generate polymer precipitation, creating at least one microsphere with the nanoparticles embedded onto it, subjecting the exposed hemisphere of the embedded nanoparticles to a further amphiphilic particles related modification, and dissolving the at least one microsphere in a polycarbonate-based solution in order to free said embedded nanoparticles from the at least one microsphere.

A composite material is provided including a polymer matrix and undercooled liquid metallic core-shell particles disposed in the matrix, wherein the particles each have an outer shell and a liquid metallic material as a core contained within the outer shell. The outer shell is frangible such that the liquid metallic material is released from at least some of the particles in response to a mechanical load applied to the composite and solidifies in-situ in the polymer matrix. As a result, the composite material can be self-strengthening and self-healing and can be reconfigurable in shape at ambient temperature.

Disclosed are: an ionomer nanoparticle dispersion solution formed by dispersing a perfluorinated ionomer having an ion conductive functional group in a solvent mixture including water and an alcohol, and carrying out a reaction under a supercritical condition; and a preparation method thereof. The ionomer nanoparticle dispersion solution has a high azeotropic mixture content in a continuous phase, which is a liquid phase, so as to readily remove a solvent therefrom, and thus a product using the ionomer nanoparticle dispersion solution can be readily fabricated and preparation costs can be reduced. In addition, uniformity of the product is improved because a perfluorinated ionomer having various ion conductive functional groups and various salts thereof is nano-dispersed, in a narrow molecular weight distribution, in the ionomer nanoparticle dispersion solution.

The present disclosure is directed to multiphase dispersions and nanocomposites comprised of a continuous matrix or binder and an endohedrally impregnated cellular carbon filler. These nanocomposites may exhibit superior mechanical, electrical, thermal, or other properties, and may be used in a variety of products, including hierarchical fiber-reinforced composites with nanocomposite matrices.

Adhesive compositions and patches, and associated systems, kits, and methods, are generally described. Certain of the adhesive compositions and patches can be used to treat tissues (e.g., in hemostatic or other tissue treatment applications), according to certain embodiments.

Copolymers comprising recurring units of a phenyl glycidyl ether and alkylene oxides are disclosed. Some of the copolymers comprise a di- or polyfunctional nucleophilic initiator and recurring units of the phenyl glycidyl ether and an alkylene oxide. The di- or polyfunctional nucleophilic initiator is an alcohol, phenol, amine, thiol, thiophenol, sulfinic acid, or deprotonated species thereof. Other copolymers comprise a monofunctional nucleophilic initiator selected from thiols, thiophenols, aralkylated phenols, sulfinic acids, secondary amines, C.sub.10-C.sub.20 terpene alcohols, and deprotonated species thereof. Pigments dispersions comprising the copolymers are also disclosed. The copolymers meet the growing needs of the industry with their ease of manufacture, diverse structures, and desirable performance attributes for dispersing a wide range of organic and inorganic pigments. Agricultural applications for the copolymers are also disclosed.

A process for the recovery of a perfluorosulphonic acid ionomer from a component comprising a perfluorosulphonic acid ionomer is disclosed, the process comprising immersing the component comprising the perfluorosulphonic acid ionomer in a solvent comprising an aliphatic diol and heating. Also disclosed is the use of the recovered perfluorosulphonic acid ionomer, for example in to prepared a proton conducting membrane or a catalyst ink.

The invention relates to a self-supporting, biodegradable film comprising a C.sub.10-C.sub.22-acylated derivative of hyaluronic acid according to the general formula (I), where R is H.sup.+ or Na.sup.+, and where R.sup.1 is H or C(O)C.sub.xH.sub.y, where x is an integer within the range from 9 to 21 and y is an integer within the range from 11 to 43 and C.sub.xH.sub.y is a linear or branched, saturated or unsaturated C.sub.9-C.sub.21 chain, wherein in at least one repeating unit one or more of R.sup.1 is C(O)C.sub.xH.sub.y and where n is within the range from 12 to 4000; a method of preparation thereof and use thereof. ##STR00001##

The invention relates to a process for making a membrane M comprising the following steps: providing a dope solution D comprising a polymer P selected from polyphenylenesulfone or mixtures of polyphenylenesulfone with nonionic polyarylene ethers, a first solvent selected from aprotic polar solvents, and a cosolvent selected from C.sub.2-C.sub.8 alkanediol, C.sub.3-C.sub.8 alkanetriol, polyethylene glycol, or mixtures thereof; and preparing the membrane by bringing the dope solution D into contact with a coagulating agent. The invention further relates to a membrane M obtainable in said process.