A polymeric composition includes a diene elastomer; an azodicarboxy compound; and a reinforcing filler comprising silica. The composition is not foamed. A method for preparing a polymeric composition includes mixing in one or more steps: a diene elastomer; an azodicarboxy compound; and a reinforcing filler. The mixing temperature is less than 160° C. in mixing steps in which the azodicarboxy compound is present. In an embodiment, the mixing temperature is kept below the decomposition temperature of the azodicarboxy compound.

A method of immobilization of an insoluble dopant. In some embodiments, the insoluble dopant comprises a coordination polymer. In some embodiments, the insoluble dopant comprises a vapochromic coordination polymer. The method may comprise dissolving a polymer carrier in a solvent. The polymer carrier may comprise a thermoplastic such as, but not limited to, polylactic acid, polyethylene glycol or polycarbonate. The insoluble dopant (e.g. a coordination polymer such as a vapochromic coordination polymer) may then be mixed into the dissolved polymer. Phase separation of the mixture of the dopant and dissolved polymer may be induced to form a hydrogel. The hydrogel may be employed as is (e.g. as a raw material for hydrogel 3D printing, as a sensing material, etc.) or may undergo further processing (e.g. solidification, grinding, extrusion, etc.) before being employed, for example, as a raw material for 3D printing, as a sensing material, etc.

An ultra-high molecular weight, ultra-fine particle size polyethylene has a viscosity average molecular weight (Mv) greater than 1×10.sup.6. The polyethylene is spherical or are sphere-like particles having a mean particle size of 10-100 μm, having a standard deviation of 2-15 μm and a bulk density of 0.1-0.3 g/mL. Using the polyethylene as a basic polyethylene, a grafted polyethylene can be obtained by means of a solid-phase grafting method; and a glass fiber-reinforced polyethylene composition comprising the polyethylene and glass fibers, and a sheet or pipe prepared therefrom; a solubilized ultra-high molecular weight, ultra-fine particle size polyethylene; and a fiber and a film prepared from the solubilized ultra-high molecular weight, ultra-fine particle size polyethylene may also be obtained. The method has simple steps, is easy to control, has a relatively low cost and a high repeatability, and can realize industrialisation.

Perovskite-polymer composites including perovskite nanocrystals dispersed in a polymer matrix, wherein the perovskite nanocrystals have an average size of from about nm to about 20 nm. Methods for producing a perovskite-polymer composites that may include contacting a solid material comprising a polymer matrix with a solution comprising a perovskite precursor; allowing the solution to penetrate the solid material to yield a swollen solid material comprising the perovskite precursor dispersed within the polymer matrix; optionally contacting the swollen solid material with an antisolvent; and annealing the swollen solid material to crystallize the perovskite precursor and to yield the perovskite-polymer composite comprising perovskite nanocrystals dispersed in the polymer matrix.

Disclosed is a method for producing biodegradable polymer nanocomposite, the method comprising dispersing a plurality of graphene nanoplatelets into a matrix of biodegradable polymer and extruding the matrix of biodegradable polymer containing the plurality of graphene nanoplatelets to obtain the biodegradable polymer nanocomposite.

The present invention relates to a novel polyaryletherketone (PAEK) polymer composition with a significantly increased crystallization rate, and preferably, to a polyetherketoneketone (PEKK) polymer composition. According to the present invention, there is provided a polymer composition including a liquid crystal polymer (LCP), an inorganic nucleating agent, a reinforcing agent, and a filler in polyaryletherketone (PAEK). Therefore, the present invention provides an effect of improving a crystallization rate of the polymer composition and improving molding processability, thereby improving productivity, shape, dimensional stability, or the like of products.

Disclosed is a rubber composition which suppresses poor mixing or poor dispersion from occurring between an organic polymer material derived from natural rubber and an inorganic material such as silica and exhibits excellent viscoelastic properties, and a silane coupling agent composition used in the same. Also disclosed is a silane coupling agent composition comprising a protein modifying agent and a silane compound represented by Formula (1):

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wherein each of the variables is as defined herein.

The present invention relates to polypropylene particles and a method for preparing same, the polypropylene particles being formed from a polypropylene resin, and having a melting index (M.I.) of 1000 g/10 min or more when the particles are re-melted under a temperature condition of 150° C. to 250° C. and a condition of atmospheric pressure to a pressure of 15 MPa.

To provide a rubber composition excellent in elasticity and low loss property.

A rubber composition comprising 100 parts by weight of a chloroprene rubber and from 1.2 to 3.0 parts by weight of cellulose nanofibers, characterized in that a vulcanized sheet obtained by vulcanizing the rubber composition has a 100% tensile stress (M100) increased by 1.5 MPa or more per part by weight of the cellulose nanofibers added, where the increase of M100 is calculated by subtracting M100 of a vulcanized sheet containing no cellulose nanofibers from M100 of the vulcanized sheet containing the cellulose nanofibers, and dividing the difference by the amount of the cellulose nanofibers contained.

A machinable wax with plastic additive and method of manufacture is shown and described. The machinable wax with a plastic additive includes between twenty-five (25) percent and thirty-five (35) percent of the polyethylene (PE) Wax by volume. The machinable wax includes between thirty-five (35) percent and forty-five (45) percent of LD polyethylene by volume. The machinable wax also includes between ten (10) percent and twenty (20) percent of micro crystalline wax by volume and between seven (7) percent and twelve (12) percent of paraffin wax by volume. In some embodiments the machinable wax includes between three (3) percent and six (6) percent of acetic acid ethenyl ester by volume. In some instances, the machinable wax has less than or equal to one (1) percent of colorant by volume added.