A method to form a phase change material (PCM). The method includes preparing a polymer solution by mixing an amount of a polymer in a solvent and mixing the polymer solution with an UiO-66 metal-organic framework (MOF) to form a composite. The polymer is a polyethylene glycol (PEG). The method further includes subjecting the composite to ultrasonic agitation and evaporating the solvent from the composite to form the PCM. After the evaporation of the solvent, particles of the PCM exhibit rounded octahedral structures.

An organic-inorganic hybrid material is disclosure. The organic-inorganic hybrid material contains 5˜50 wt % of inorganic compounds and has a characteristic peak at 1050±50 cm.sup.−1 in FTIR spectrum. Furthermore, the invention also provides a fabricating process of the organic-inorganic hybrid material as well as its starting material “isocyanates”. In particular, the isocyanates are prepared from carbonate containing compounds and amines.

Polymers suitable for forming carbon nanotube-functionalized reverse thermal gel compositions, compositions including the polymers, and methods of forming and using the polymers and compositions are disclosed. The compositions have reverse thermal gelling properties and transform from a liquid/solution to a gel—e.g., near or below body temperature. The polymers and compositions can be injected into or proximate an area in need of treatment.

The present invention addresses the problem of providing a desiccant that can be used for passivation of an electronic device such as an organic electroluminescence element against moisture permeation, as well as an organic thin film including the desiccant, an organic layered film in which the organic thin film is layered, and an electronic device that is provided therewith. This desiccant is characterized by including a compound that emits a hydrophobic substance by absorbing water. This organic thin film is characterized by including this desiccant.

Parts made by additive manufacturing are often structural in nature, rather than having functional properties conveyed by a polymer or other component present therein. Printed parts having piezoelectric properties may be formed using compositions comprising a plurality of piezoelectric particles and a polymer material comprising at least one thermoplastic polymer and at least one thermally curable polymer precursor. At a sufficient temperature, the at least one thermally curable polymer precursor may undergo a reaction, optionally also undergoing a reaction with the piezoelectric particles, and form an at least partially cured printed part. The piezoelectric particles may be mixed with the polymer material and remain substantially non-agglomerated when combined with the polymer material. The compositions may define a form factor such as a composite filament, a composite pellet, or an extrudable composite paste, which may be utilized in forming printed part by extrusion, layer-by-layer deposition, and thermal curing.

A nonlimiting example method of forming highly spherical carbon nanomaterial-graft-polyurethane (CNM-g-polyurethane) particles may comprising: mixing a mixture comprising: (a) carbon nanomaterial-graft-polyurethane (CNM-g-polyurethane), wherein the CNM-g-polyurethane particles comprises: a polyurethane grafted to a carbon nanomaterial, (b) a carrier fluid that is immiscible with the polyurethane of the CNM-g-polyurethane, optionally (c) a thermoplastic polymer not grafted to a CNM, and optionally (d) an emulsion stabilizer at a temperature greater than a melting point or softening temperature of the polyurethane of the CNM-g-polyurethane and the thermoplastic polymer, when included, and at a shear rate sufficiently high to disperse the CNM-g-polyurethane in the carrier fluid; cooling the mixture to below the melting point or softening temperature to form CNM-g-polyurethane particles; and separating the CNM-g-polyurethane particles from the carrier fluid.

A nonlimiting example method of forming highly spherical carbon nanomaterial-graft-polyamide (CNM-g-polyamide) polymer particles may comprising: mixing a mixture comprising: (a) carbon nanomaterial-graft-polyamide (CNM-g-polyamide), wherein the CNM-g-polyamide particles comprises: a polyamide grafted to a carbon nanomaterial, (b) a carrier fluid that is immiscible with the polyamide of the CNM-g-polyamide, optionally (c) a thermoplastic polymer not grafted to a CNM, and optionally (d) an emulsion stabilizer at a temperature greater than a melting point or softening temperature of the polyamide of the CNM-g-polyamide and the thermoplastic polymer, when included, and at a shear rate sufficiently high to disperse the CNM-g-polyamide in the carrier fluid; cooling the mixture to below the melting point or softening temperature to form CNM-g-polyamide particles; and separating the CNM-g-polyamide particles from the carrier fluid.

A polymer/activated carbon composite made up of a branched polyethylenimine and magnetic cores involving Fe.sub.3O.sub.4 disposed activated carbon. The magnetic cores have activated carbonyl groups on the surface. A process for removing organic dyes, such as methyl red, as well as heavy metal ions from a polluted aqueous solution or an industrial wastewater utilizing the composite is introduced. A method of synthesizing the polymer/activated carbon composites is also specified.

A metal coordination polymer, in particular, a layered metal coordination polymer, can be used as a precursor to form nanostructures of various morphologies and composition. Metal based nanostructures can be prepared from the metal coordination polymers. The nanostructures may have various catalytic properties. The layered metal coordination polymer includes two or more layers, each layer including metal atoms coordinated to an organic linker to form a metal coordination polymer layer.

Provided are a high-entropy carbide ceramic, a rare earth-containing high-entropy carbide ceramic, fibers thereof, precursors thereof, and preparation methods thereof. The precursor includes at least four elements selected from Ti, Zr, Hf, V, Nb, Ta, Mo, and W, with each metal element accounting for 5-35% of the total molar quantity of metal elements in the precursor. The rare earth-containing high-entropy carbide ceramic precursor includes at least four transition metal elements and at least one rare-earth metal element. The high-entropy ceramic is a single-crystal-phase high-performance ceramic prepared from the precursor, with each element being homogenously distributed at molecular level. The method for preparing the high-entropy ceramic fiber includes uniformly mixing high-entropy carbide ceramic precursor containing target metal elements with spinning aid and solvent to prepare a spinnable precursor solution, followed by spinning, pyrolyzation, and high-temperature solid solution to prepare the high-entropy carbide ceramic fiber.