Abstract: The present invention provides an improved method of quantitative and/or qualitative analysis of a target molecule using nitrocellulose membrane (NCM). In particular, the present invention provides a porous nitrocellulose membrane that includes a surface and an organic nanostructured molecule that is non-covalently attached to the surface of NCM. The organic nanostructured molecule has a branched region that includes a plurality of terminal region (e.g., terminal end) moieties that are non-covalently attached or bound to a surface of the porous NCM. The organic nanostructured molecule also comprises a linear region that includes a covalently attached capture molecule that is adapted to selectively bind to a target molecule. The NCM of the invention provides an improved reproducibility, reliability, and selectivity compared an NCM in the absence of the organic nanostructured molecule.

Abstract: Provided is a method of producing a vinyl chloride-based polymer including adding a vinyl chloride monomer and a monomer represented by Chemical Formula 1 to a reactor and performing polymerization, wherein an input amount of the monomer represented by Chemical Formula 1 is 1 to 4 parts by weight based on 100 parts by weight of the vinyl chloride monomer, and the monomer represented by Chemical Formula 1 is continuously added to the reactor.

Abstract: A cutting tool includes a substrate and a coating film, wherein the coating film has a first layer formed from a plurality of hard grains, the hard grains are made of TiSiCN having a cubic crystal structure, the hard grains have a lamellar structure in which a layer having a relatively high silicon concentration and a layer having a relatively low silicon concentration are alternately stacked, and a maximum value of percentage of number ASi of silicon atoms to a sum of the number ASi of silicon atoms and number ATi of titanium atoms in a grain boundary region between the hard grains, {ASi/(ASi+ATi)}×100, is larger than an average value of percentage of number BSi of silicon atoms to a sum of the number BSi of silicon atoms and number BTi of titanium atoms in the first layer, {BSi/(BSi+BTi)}×100.

Abstract: Provided are an organic compound, an electroluminescent material, and a use thereof. The organic compound has a structure represented by Formula I and is a carbazole olefin-like compound which is beneficial for improving the amorphous performance, thermal stability, and glass transition temperature of the material. The organic compound has appropriate HOMO energy level and LUMO energy level and a relatively high triplet energy level and can inhabit the transfer of triplet energy from a guest back to a host and reduce a driving voltage of a device. The organic compound, as a host material, has a relatively high carrier transport rate and balanced carrier transport performance, so as to facilitate the balance of hole and electron currents in the device, obtain a wider carrier recombination region, significantly improve light emitting efficiency and external quantum efficiency of the device, and reduce a turn-on voltage and power consumption of the device.

Abstract: Curable formulations which form cured materials that are breakable upon immersion in water are disclosed. The cured materials break into a plurality of particles being a few millimeters or less in size. Methods of fabricating three-dimensional objects utilizing the curable formulations are also disclosed, as well as model objects fabricated thereby. The curable formulations include at least a mono-functional curable material and a multi-functional curable material, as described in the specification.

Abstract: A proton exchange solid support includes a first solid support including a polymer, a second solid support, and a tetravalent boron-based acid group that links the first solid support to the second solid support.

Abstract: The present invention relates to a chemically modified anion exchange membrane and a method of preparing the same and, more particularly, an anion exchange membrane in which sulfonic acid groups in a perfluorinated sulfonic acid electrolyte membrane are substituted with anion conductive groups such as ammonium group, phosphonium group, imidazolium group, pyridinium group and sulfonium group, and a method of preparing an anion exchange membrane by chemically modifying sulfonic acid groups in a perfluorinated sulfonic acid electrolyte membrane.

Abstract: The present disclosure provides an ion-exchange membrane that includes a supporting substrate impregnated with an ion-exchange material. The supporting substrate includes an imprinted non-woven layer, and the imprinting includes a plurality of deformations at a surface density of at least 16 per cm2. The supporting substrate may lack a reinforcing layer. In some examples, the supporting substrate may include only a single layer of the imprinted non-woven fabric.

Abstract: The present invention relates to a multilayer element (LE), the use of the multilayer element (LE) for producing an article, an article comprising multilayer element (LE), a layer element of at least two layers, the use of the polymer composition of the invention to produce a multilayer element, as well as to a process for producing the multilayer element (LE) and an article thereof.

Abstract: Provided are a polymer composition that can suppress bubbling during membrane formation and peeling of a laminated membrane and an ion-exchange membrane. The polymer composition is a polymer composition including: a fluorine-containing copolymer including a unit (a) derived from a perfluorovinyl compound having a side chain having an ionic group and a unit (b) derived from a fluoroolefin; and a low molecular weight compound (a) having a functional group represented by —COOX (X is H, NH4, or a monovalent metal ion), wherein a content of the low molecular weight compound (a) is 600 ppm or less based on a mass of the polymer composition.

Abstract: An organic light-emitting device including: a first electrode; a second electrode facing the first electrode; a first emission unit and a second emission unit between the first electrode and the second electrode; and a first charge generation layer between the first emission unit and the second emission unit; wherein the first emission unit includes a first emission layer and a first inorganic buffer layer, and the second emission unit includes a second emission layer and a second inorganic buffer layer.

Abstract: The present invention generally relates to various polymer solid electrolyte materials suitable for various electrochemical devices and methods for making or using the same. Certain embodiments of the invention are generally directed to solid electrolytes having relatively high ionic conductivity and/or other mechanical or electrical properties, e.g., tensile strength or decomposition potential. Certain aspects include a polymer, a plasticizer, and an electrolyte salt. In some cases, the polymer may exhibit certain structures such as: where R1 can be one of the following groups: where n is an integer between 1 and 10000, m is a integer between 1 and 5000, and R2 to R6 are each independently selected from the group consisting of hydrogen, methyl, ethyl, phenyl, benzyl, acryl, epoxy ethyl, isocyanate, cyclic carbonate, lactone, lactam, and vinyl; and * indicates a point of attachment.

Abstract: A method for applying raised features to a semiconductor substrate chuck, each feature acting to space a substrate from the chuck in use, the method comprising the steps of: i) providing an assembly having a carrier layer, a feature adhered to the carrier layer, and a peel-ply layer adhered to the carrier layer such that the feature is enclosed between the carrier layer and the peel-ply layer, ii) removing the peel-ply layer, and iii) adhering the feature to the chuck.

Abstract: An ion exchange membrane has multiple layers of ionic polymers which each contain substantially different chemical compositions. i.e. varying side chain lengths, varying backbone chemistries or varying ionic functionality. Utilizing completely different chemistries has utility in many applications such as fuel cells where for example, one layer can help reduce fuel crossover through the membrane. Or one layer can impart substantial hydrophobicity to the electrode formulation. Or one layer can selectively diffuse a reactant while excluding others. Also, one chemistry may allow for impartation of significant mechanical properties or chemical resistance to another more ionically conductive ionomer. The ion exchange membrane may include at least two layers with substantially different chemical properties.

Abstract: A process of forming a cross-linked electronically active hydrophilic co-polymer is provided and includes the steps of: a. mixing an intrinsically electronically active material and at least one compound of formula (I) with water to form an intermediate mixture; b. adding at least one hydrophilic monomer, at least one hydrophobic monomer, and at least one cross-linker to the intermediate mixture to form a co-monomer mixture; and c. polymerising the co-monomer mixture. Formula (I) is defined as: where R1 and R2 are independently optionally substituted C1-C6 alkyl and X? is an anion.

Abstract: Among the various aspects of the present disclosure is the provision of a hydrogel-based substrate comprising an aldehyde-containing component, such as N-ethanal acrylamide. The hydrogel component allows for functionalization of a hydrogel through conjugation of proteins (e.g., collagen) to the hydrogel in the absence of a post hoc crosslinking component.

Abstract: The present invention provides a resin composition for an adhesive, being useful as a component of an adhesive having a favorable adhesion property to glass and giving favorable appearance after adhesion. The resin composition for an adhesive contains a polyhydroxyurethane resin. This polyhydroxyurethane resin contains a structural unit formed by polymerizing a compound (A) having at least two five-membered cyclic carbonate structures and a compound (B) having at least two primary amino groups, the polyurethane resin contains a urethane bond, a hydroxy group, and a secondary amino group in the structural unit. Further, this polyhydroxyurethane resin has an amine number of 1 to 50 mgKOH/g and has a hydroxyl number of 10 to 230 mgKOH/g.

Abstract: The present invention relates to a curable resin composition. More specifically, the present invention relates to a composition comprising methylene malonate functional reactive resin, to its preparation methods, and to the use of the composition in the construction field.

Abstract: A thermoset resin for forming parts to be metal plated includes a vat photopolymerization (VPP) thermoset resin and an etchable phase disposed in the VPP thermoset resin. The etchable phase is etched from a surface of a part formed from the VPP thermoset resin such that a plurality of micro-mechanical locking sites is formed on the surface of the part. The etchable phase is at least one of organic particles, organic resins, inorganic particles, and copolymers of the VPP thermoset resin. For example, the etchable phase can be a polybutadiene phase and/or a mineral such as calcium carbonate.

Abstract: An interlayer film for laminated glass of the present invention comprises a thermoplastic resin, a carboxylic acid, and an alkali (alkaline earth) metal, wherein, when a molar concentration per unit volume of the alkali (alkaline earth) metal in the interlayer film for laminated glass, measured by ICP atomic emission spectrophotometry is A (mol/m3); a molar concentration per unit volume of the carboxylic acid in the interlayer film for laminated glass, measured by GC-MS is B (mol/m3); a molar concentration per unit volume of the carboxylic acid in the interlayer film for laminated glass, measured by GC-MS after a hydrochloric acid aqueous solution is added to the interlayer film for laminated glass to be left at 23° C. for 12 hours is Y; and a molar concentration per unit volume of the carboxylic acid, obtained by subtracting the molar concentration B from the concentration Y is D (mol/m3), the molar concentration A is more than 0.35 mol/m3 and less than 1.