Abstract: Methods of forming nanoporous materials are described herein that include forming a polymer network with a chemically removable portion. The chemically removable portion may be polycarbonate polymer that is removable on application of heat or exposure to a base, or a polyhexahydrotriazine (PHT) or polyhemiaminal (PHA) polymer that is removable on exposure to an acid. The method generally includes forming a reaction mixture comprising a formaldehyde, a solvent, a primary aromatic diamine, and a diamine having a primary amino group and a secondary amino group, the secondary amino group having a base-reactive substituent, and heating the reaction mixture to a temperature of between about 50 deg C. and about 150 deg C. to form a polymer. Removing any portion of the polymer results in formation of nanoscopic pores as polymer chains are decomposed, leaving pores in the polymer matrix.

Abstract: A porous material includes a polyhexahydrotriazine material. Pores in the porous material can be of various sizes including nanoscale sizes. The porous material may be used in a variety of applications, such as those requiring materials with a high strength-to-weight ratio. The porous material can include a filler material dispersed therein. The filler material can be, for example, a particle, a fiber, a fabric, or the like. In some examples, the filler material can be a carbon fiber or a carbon nanotube. A method of making a porous material includes forming a resin including a polyhemiaminal or polyhexahydrotriazine component and a polythioaminal component. The resin can be heated to promote segregation of the components into different phases with predominately one or the other component in each phase. Processing of the resin after phase segregation to decompose the polythioaminal component can form pores in the resin.

Abstract: Provided is an organic light-emitting device including a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer. The emission layer includes a first compound represented by Formula 1-1 or Formula 1-2 below, a second compound represented by Formula 2 below, and a third compound represented by Formula 3 below: where Ar1 to Ar8, R1 to R3, A, L1, L2, a1, a2, b1, b2, c1, c2, l1, and l2 are as defined in the specification.

Abstract: Disclosed herein are aspects and embodiments of hydrophilic polymeric blend and polymeric membranes which may be formed from the hydrophilic polymeric blend. In one example, the polymeric blend includes a hydrophobic membrane forming polymer and a polyoxazoline as a blend compatible hydrophilizing additive.

Abstract: The present disclosure provides a modified starch composition. The modified starch composition includes starch with a terminal siloxane having 100 parts by weight, water having 30-70 parts by weight, and a polyol having 5-35 parts by weight. The present disclosure also provides a starch composite foam material and method for preparing the same.

Abstract: An amine-based compound is represented by Formula 1: wherein L1 to L3, Ar1 to Ar3, a1 to a3, and c1 to c3 are as defined in the specification. An organic light-emitting device includes the amine-based compound.

Abstract: Disclosed are an optical film and a preparation method thereof. The optical film comprises a base layer, a plurality of polymer particles disposed in the base layer, and voids formed in the base layer and enclosing the respective polymer particles, wherein the polymer particles comprise a crosslinked polymer. The optical film has uniform voids, enhanced processing and dimensional stabilities, as well as improved optical properties such as whiteness, hiding power, reflectance and the like. Thus, the optical film can be useful for a reflector sheet for a BLU of an LCD device, and the like.

Abstract: Reversibly cross-linkable foam is provided. The reversibly cross-linked foam includes a first polymeric material, at least one reversibly cross-linkable monomer polymerized with the first polymeric material, and at least one blowing agent. The reversibly cross-linkable co-polymeric foam is thermally stable at temperatures of at least 10 degrees higher than otherwise identical polymeric foam that does not include the reversibly cross-linkable agent polymerized with the first polymeric material.

Abstract: A formulation starts as a gel and transforms into a foam under influence of light and heat to expand out into the oral cavity of a user for advantageous health benefits. A closed system mouthpiece includes light and heat generation to activate the formulation to increase its volume. Application of heat above a threshold temperature causes the gel to transform into foam and expand out of the mouthpiece and into the oral cavity. With the foam so dispersed within the oral cavity, activation of a light source embedded within the mouthpiece enhances the bacteria killing properties of the now foam material. The foam spreads onto the tongue of the user as well and acts to kill any damaging bacteria found there. As a result, the pH balance of the mouth is restored to a neutral level in the range of 6.75 to 7.25 or maintained at that pH level.

Abstract: Disclosed is a high filling and high resilience soft foaming polyethylene material, comprising the following parts of raw materials by weight: 15-20 parts polyethylene, 5-20 parts elastomers, 60-80 parts modified calcium carbonate, 1-10 parts chemical foaming agent, 0.5-1.5 parts crosslinking agent and 1-5 parts physical foaming agent. Also disclosed is a method of preparing high filling and high resilience soft foaming polyethylene material. The present invention can prepare a high calcium carbonate filling and high resilience soft foaming polyethylene material with calcium carbonate filler content as high as 55-75%, improving rigidity, hardness and compressive strength of the material while maintaining the elasticity of the foaming material, and reducing material density. The present invention has a simple process, greatly reduces costs and is economical and practical.

Abstract: Cellular and multi-cellular polystyrene and polystyrenic foams and methods of forming such foams are disclosed. The foams include an expanded polystyrene formed from expansion of an expandable polystyrene including an adsorbent comprising alumina, wherein the multi-cellular polystyrene exhibits a multi-cellular size distribution. The process for forming a foamed article includes providing a formed styrenic polymer and contacting the formed styrenic polymer with a first blowing agent and an adsorbent comprising alumina to form extrusion polystyrene. The process further includes forming the extrusion styrenic polymer into an expanded styrenic polymer and forming the expanded styrenic polymer into a foamed article.

Abstract: The present invention discloses a method for preparing a microporous polyolefin film comprising: a step of injecting a composition comprising polyolefin 30 to 60 wt % and a diluent mixture comprising a diluent, which can make liquid-liquid phase separation with the polyolefin thermodynamically 40 to 70 wt %, into an extruding machine, and melting and kneading thereof to prepare a single phase melt; and a step of extruding the melt while conducting liquid-liquid phase separation by passing through a section having the temperature below the liquid-liquid phase separation temperature and forming thereof in the form of a sheet, and a microporous polyolefin film prepared according to the method.

Abstract: Disclosed is a medical instrument coating, being coated on the surface of a nickel-titanium alloy component of a medical instrument. The medical instrument coating comprises an elementary copper phase, an amorphous titanium-containing substance and a transition layer comprising a copper-nickel intermetallic phase. Also mentioned is a preparation method for the medical instrument coating.

Abstract: A thermoplastic sulfur-polymer composite comprises a thermoplastic polymer, such as polyethylene and polystyrene; and a sulfur element. Such sulfur element functions as passive sulfur filler in this composite. The thermoplastic polymer is a polymer matrix; and the sulfur filler is dispersed in the polymer matrix. There is no chemical reaction occurs after the addition of the sulfur filler into the host polymer and no chemical bond formed between the polymer and the sulfur filler. The thermoplastic sulfur-polymer composite can be a nanocomposite by either adding certain nanofillers into the composite or making the sulfur filler as sulfur nanoparticles. With its similar physical properties and lower manufacturing costs, the thermoplastic sulfur-polymer composites are good alternatives of the respective pure polymers.

Abstract: Methods of forming nanoporous materials are described herein that include forming a polymer network with a chemically removable portion. The chemically removable portion may be polycarbonate polymer that is removable on application of heat or exposure to a base, or a polyhexahydrotriazine (PHT) or polyhemiaminal (PHA) polymer that is removable on exposure to an acid. The method generally includes forming a reaction mixture comprising a formaldehyde, a solvent, a primary aromatic diamine, and a diamine having a primary amino group and a secondary amino group, the secondary amino group having a base-reactive substituent, and heating the reaction mixture to a temperature of between about 50 deg C. and about 150 deg C. to form a polymer. Removing any portion of the polymer results in formation of nanoscopic pores as polymer chains are decomposed, leaving pores in the polymer matrix.

Abstract: Porous three-dimensional networks of polyimide and porous three-dimensional networks of carbon and methods of their manufacture are described. For example, polyimide aerogels are prepared by mixing a dianhydride and a diisocyanate in a solvent comprising a pyrrolidone and acetonitrile at room temperature to form a sol-gel material and supercritically drying the sol-gel material to form the polyimide aerogel. Porous three-dimensional polyimide networks, such as polyimide aerogels, may also exhibit a fibrous morphology. Having a porous three-dimensional polyimide network undergo an additional step of pyrolysis may result in the three dimensional network being converted to a purely carbon skeleton, yielding a porous three-dimensional carbon network. The carbon network, having been derived from a fibrous polyimide network, may also exhibit a fibrous morphology.

Abstract: The present invention relates to methods of forming aerogels.

Abstract: A method for producing a breathable film based on polyvinyl chloride (PVC), including the following steps. Preparing a paste-like compound including a first fraction composed of PVC, a second fraction composed of a foreign material, and a third fraction composed of adjuvants and/or additives that that are mixed together to form the paste-like compound, applying the paste-like compound to a base, and drying and gelling the paste-like compound, which has been applied to the base, through the addition of heat, thus forming the film in which pores extending from the one surface of the film to the other are formed, which give the film breathability.

Abstract: The invention relates to a method of preparing expanded thermoplastic microspheres from thermally expandable thermoplastic microspheres comprising a polymer shell encapsulating a foaming agent, the method comprising heating the expandable microspheres within a flexible container (2) to effect expansion of said microspheres and withdrawing gas from said flexible container (2). The invention further relates to an expansion device for preparing such expanded thermoplastic microspheres.

Abstract: A method for preparing macroporous polymethyl methacrylate (PMMA) particles includes the steps of: (a) dissolving a polymethyl methacrylate polymer and Pluronic polymer into an organic solvent; (b) introducing the mixed solution of step (a) to an aqueous solution containing a surfactant to carry out emulsion polymerization; (c) heating the resultant product of step (b) to allow evaporation of the organic solvent; and (d) washing and drying the porous polymethyl methacrylate particles remaining after the evaporation.