C08J3/005

COMPATIBILIZATION OF IMMISCIBLE POLYMERS USING CARBON NANOTUBES
20230183448 · 2023-06-15 ·

The present disclosure provides a polymer blend that includes at least two polymers which are immiscible to one another and a carbon nanotube pulp comprising entangled carbon nanotubes as a compatibilizing agent and to a method of preparing the same.

Easily-plated PC/ABS alloy and its preparation method

The present invention relates to an easily-plated PC/ABS alloy and its preparation method. The PC/ABS alloy includes following components: 30-70 parts by weight (pbw) of PC resin, 15-65 pbw of ABS resin, 5-10 pbw of PEO resin, 0.1-1 pbw of antioxidant, and 0.1-1 pbw of lubricant. For preparation, blending the PC resin, ABS resin, PEO resin, antioxidant and lubricant in a mixer; and putting a mixture in a twin-screw extruder for granulation, thus producing easily-plated PC/ABS alloy. The method is simple and practicable. PEO resin makes PC/ABS surface have the property of hydrophilicity, which makes the etching solution easier to wet the surface when under etching, so that the etching becomes much easier. The binding force of hydrophilic group on the surface of PEO to the metal is strong. The binding force of PC/ABS alloy material is improved due to the combination between the chemical bond and physical force.

THERMOPLASTIC POLYMERS AND METHOD TO MAKE THEM
20230183429 · 2023-06-15 ·

Polymer powders useful for additive manufacturing may be made by contacting carbon dioxide and a crystallizable polymer having at least one carbonyl, sulfur oxide or sulfone group; permeating the carbon dioxide into the polymer for a crystallizing time sufficient to induce crystallization forming an induced crystalized polymer; removing the carbon dioxide; and forming induced crystalized polymer particles having a D90 particle size of at most 300 micrometers and average particle size of 1 micrometer to 100 micrometers equivalent spherical diameter. The carbon dioxide is desirably supercritical carbon dioxide for at least a portion of the crystallizing time. The polymer powders upon heating during additive manufacturing may result in a polymer having less crystallinity or become amorphous.

An On-Line Control and Reaction Process for pH Adjustment
20170342663 · 2017-11-30 · ·

An on-line control and reaction process for pH adjustment and a control device for automatically adjusting pH value are provided. The process includes mixing a first enhancer and a second enhancer, optionally after diluting the first enhancer and/or the second enhancer with water, to form a mixture, setting a base pH value (δ1) and a target pH value (δ2), and adding pH adjuster into the mixture via a pH control unit and mixing to obtain a product with the target pH value. The pH control unit adjusts the adding of the pH adjuster by measuring or inputting certain parameters.

Upgraded recycled relatively polyethylene rich polyolefin materials
11674027 · 2023-06-13 · ·

A polyethylene-polypropylene composition obtainable by blending a) 80 to 97 wt.-% of a blend (A) comprising A-1) polypropylene and A-2) polyethylene, wherein the ratio of polypropylene to polyethylene is from 3:7 to 13:7, and wherein blend (A) is a recycled material, which is recovered from a waste plastic material derived from post-consumer and/or post-industrial waste; and b) 3 to 20 wt.-% of a compatibilizer (B) being a heterophasic random copolymer comprising a random polypropylene copolymer matrix phase and an elastomer phase dispersed therein, whereby the heterophasic random copolymer has—a xylene insolubles content (XCI) of from 65 to 88 wt.-% (ISO 16152, led, 25° C.), and—a xylene soluble content XCS of 12 to 35 wt.-% (ISO 16152, led, 25° C.), the XCS fraction having an intrinsic viscosity (measured in decalin according to DIN ISO 1628/1 at 135° C.) of 1.2 dl/g to less than 3.0 dl/g, and—a flexural modulus of from 300 to 600 MPa (ISO 178, measured on injection moulded specimens, 23° C.); whereby the ratio of MFR.sub.2 (blend (A))/MFR.sub.2 (compatibilizer (B)) (ISO1133, 2.16 kg load at 230° C.), is in the range of 0.5 to 1.5.

Low compression set thermoplastic gel and cable gel seal arrangement

Disclosed herein are various cable gel seal arrangements and thermoplastic gels useful therein. The thermoplastic gels are prepared from a composition including a styrene triblock copolymer, a styrene diblock copolymer, an oil extender, and an additive selected from poly(2,6-dimethyl-1,4-phenylene oxide), a C9 resin, poly(alpha-methylstyrene), a coumarone-indene resin, and combinations thereof, wherein the additive has a T.sub.g from about 95° C. to about 200° C. The thermoplastic gels advantageously exhibit low compression set.

Blending of small particle starch powder with synthetic polymers for increased strength and other properties

Described herein are blends of starch or starch-based materials with polymeric materials, where the starch or starch-based material is intimately blended with the polymeric material, so as to exhibit very small particles sizes (e.g., less than 2 μm, or less than 1 μm) for the starch or starch-based material in the matrix of the polymeric material. Such intimate dispersion of very small particles provides for far more of the particles dispersed more evenly throughout the matrix of the polymeric material, which may enhance various performance characteristics of the blended composite material. Methods of producing articles from such blends exhibiting such small particles and excellent dispersion are also disclosed.

THERMOPLASTIC POLYMER COMPOSITION COMPRISING POLYROTAXANE

A composition includes a thermoplastic polymer and a polyrotaxane. The polyrotaxane includes a plurality of cyclic molecules and a chain polymer passing through the plurality of the cyclic molecules in a skewering manner, at least a part of the hydroxyl groups of the plurality of cyclic molecules being substituted with a hydrophobic group. A group that enhances miscibility of the polyrotaxane to the thermoplastic polymeris bound to at least a part of the hydrophobic groups of each of the plurality of cyclic molecules.

CARBON NANOTUBE/POLYETHERIMIDE/THERMOSETTING RESIN DIELECTRIC COMPOSITE AND PREPARATION METHOD THEREFOR
20170335069 · 2017-11-23 ·

The invention discloses a carbon nanotube/polyetherimide/thermosetting resin dielectric composite and a preparation method therefor. 100 parts by weight of polyetherimide and 1-7 parts by weight of carbon nanotube are mixed uniformly in an Haake torque melt cavity to obtain a carbon nanotubes/polyetherimide composite; 20 parts of the carbon nanotube/polyetherimide composite are dissolved in 100-150 parts of dichloromethane, then the mixed solution is added in 100 parts of molten thermocurable thermosetting resin, mixing, and heat preserving, stirring are performed until a mixture is formed in a uniform state, and curing and post-treating are performed to obtain a carbon nanotube/thermosetting resin dielectric composite, wherein the substrate thereof has a typical reverse phase structure, while the carbon nanotubes are dispersed in a polyetherimide phase. The composite has a relatively low percolation threshold, a high dielectric constant and a low dielectric loss. The preparation method of the present invention has a simple process and is suitable for large-scale production.

POLYPROPYLENE-BASED RESIN COMPOSITION, LAMINATE, AND METHODS FOR PRODUCING THEM

Provided is A polypropylene-based resin composition comprising 2 mass % to 30 mass % of a polypropylene resin (X1) having specific properties, 5 mass % to 98 mass % of a polypropylene resin (X2) having specific properties, and 0 mass % to 80 mass % of a polypropylene-based resin (Y) having specific properties, wherein the total amount of the polypropylene resin (X1), the polypropylene resin (X2) and the polypropylene-based resin (Y) is 100 mass %.