Disclosed herein are methods for designing composite materials with improved toughness.

Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, a method of producing crosslinked polymers using said curable compositions, crosslinked polymers thus produced, and orthodontic appliances comprising the crosslinked polymers.

Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, a method of producing crosslinked polymers using said curable compositions, crosslinked polymers thus produced, and orthodontic appliances comprising the crosslinked polymers.

Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, a method of producing crosslinked polymers using said curable compositions, crosslinked polymers thus produced, and orthodontic appliances comprising the crosslinked polymers.

Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, a method of producing crosslinked polymers using said curable compositions, crosslinked polymers thus produced, and orthodontic appliances comprising the crosslinked polymers.

An in-vehicle lithium ion battery member produced by molding a resin composition containing (a) a polyphenylene ether resin, the resin composition having a critical strain in a chemical resistance evaluation of 0.5% or more and a Charpy impact strength at 23° C. of 20 kJ/m.sup.2 or more.

An in-vehicle lithium ion battery member produced by molding a resin composition containing (a) a polyphenylene ether resin, the resin composition having a critical strain in a chemical resistance evaluation of 0.5% or more and a Charpy impact strength at 23° C. of 20 kJ/m.sup.2 or more.

A patterned surface structure formed from a ferrofluidic polymer resin having a plurality of magnetic nanoparticles. The polymer resin is patterned with a magnetic field that is applied to the ferrofluidic polymer resin during curing. The ferrofluidic polymer resin may be cast over a non-magnetic planar substrate. A magnetic field is applied to the ferrofluidic polymer resin to induce a pattern in a surface of the ferrofluidic polymer resin. The patterned ferrofluidic polymer resin is then cured to form the permanently patterned surface.

The present invention relates to a polycarbonate composite, a producing method thereof, and a molded article comprising same. More specifically, the present invention relates to: a polycarbonate composite comprising a matrix resin, which is a polycarbonate resin in which an anhydrosugar alcohol is copolymerized, and a nanomaterial dispersed in the matrix resin, wherein the polycarbonate composite exhibits a more remarkably improved tensile modulus and tensile strength than a conventional biopolycarbonate resin composite, by using, as a diol component, a solid dispersion or molten dispersion obtained by introducing a nanomaterial (dispersible substance) into an anhydrosugar alcohol (dispersion medium) in the form of an aqueous dispersion at the time of manufacture, and has uniform physical properties as the nanomaterial is uniformly dispersed in the composite; a producing method thereof; and a molded article comprising same.

The present invention relates to extended release microparticles comprising a drug, and a preparation method therefor, and when the extended release microparticles comprising a drug are administered in order to replace conventional drugs that should be administered daily or monthly, the drug administration effect can be continuously maintained for one week to three months. In addition, the drug administration effect is maintained for a long time and, simultaneously, microparticles are prepared so as to have the average diameter of a fixed micro-size, and thus an effective drug concentration can be constantly maintained by controlling the release of the drug from the microparticles, and a foreign body sensation and pain can be reduced during drug administration since microparticles having a uniform size are included during application as an injectable drug.