The present invention discloses a regenerated HIPS/PPO alloy material based on chemical and physical co-modification, which is mainly composed of the following components in parts by mass: waste HIPS 60-70, PPO 30-40, HIPS-based macromolecular chain extender 2-8, elastomer toughening agent 2-10, oxazoline chain extender 0.2-1, and chain-extension catalyst 0.1-0.4. The alloy material uses chemical modification of in-situ chain extension and compatibilization of the macromolecular chain extender to restore a molecular chain structure, improve a phase interface and increase compatibility of the alloy. Through physical modification introduced by adding the elastomer toughening agent, a combined effect of chemical modification and physical modification is exploited, with target properties improved, a regenerated plastic alloy material with an excellent comprehensive property prepared, and the waste fully utilized to achieve energy saving and emission reduction. A method for preparing the above-described alloy material is also disclosed.

The present disclosure provides a heat sealing aqueous resin composition containing: a rosin resin (A); a biodegradable resin (B) including a resin having a structure of General Formula (1) and/or a resin (b1) having a structure of General Formula (2); and a polyvinyl alcohol (C) in which an average saponification degree is 75 mol % or more and 85 mol % or less, in which a content of the component (b1) is more than 50% by mass when a total content of the component (A) and the component (B) is 100% by mass.

—O—(CH.sub.2).sub.x—O—CO—(CH.sub.2).sub.y—CO—  General Formula (1): (in General Formula (1), x and y may be different from each other, and are integers of 1 or more and 10 or less)

—O—(CH.sub.2).sub.z—CO—  General Formula (2): (in General Formula (2), z is an integer of 3 or more and 10 or less)

A thermoplastic composition includes 25 to 95 weight percent of a poly(etherimide); 5 to 70 weight percent of a polymer different from the poly(etherimide) that is partially miscible with the poly(etherimide); and 1 to 15 weight percent of a mineral filler having an average particle size of 0.1 to 10 micrometers; wherein each weight percent is based on the total weight of the composition. The thermoplastic composition can be prepared by melt-mixing the components of the composition. Articles including the composition are also described.

A polymer composite exhibiting piezoelectric properties can be formed for flexible and/or thin film applications, in which the polymer composite includes a polymer matrix and a piezoelectric ceramic filler embedded in the polymer matrix. The polymer matrix may include at least two polymers: a first polymer and a second polymer. The first polymer may be a fluorinated polymer, and the second polymer may be compatible with the first polymer and have a dielectric constant of less than approximately 20. The piezoelectric ceramic filler can be lithium doped potassium sodium niobite (KNLN), and be approximately 40-70% by volume of the polymer composite. The remaining 30-60% by volume may be the polymer matrix, which may itself be approximately 5-20% by weight second polymer and 80-95% fluorinated polymer.

Provided is a method for producing a thermoplastic elastomer composition that can form a molded article having both good appearance and high stiffness. The method for producing a thermoplastic elastomer composition comprises the following first step and second step, wherein the produced thermoplastic elastomer composition contains 5 mass % or less of a mineral oil (C): first step: a step of melt-kneading polypropylene (A-1) and an ethylene-based copolymer rubber (B) in the presence of an organic peroxide, the polypropylene (A-1) being polypropylene of which 20° C. xylene insoluble fraction has an intrinsic viscosity [η.sub.cxis] of 0.1 dl/g or more and less than 1.5 dl/g; and second step: a step of further adding polypropylene (A-2) of which 20° C. xylene insoluble fraction has an intrinsic viscosity [η.sub.cxis] of 1.5 dl/g or more and 7 dl/g or less, and melt-kneading the resulting mixture.

Aqueous suspensions are presented that are stable against settling without additional mixing in which the suspensions comprise a water soluble polymer that is anionic or non-ionic comprising a blend of water with at least about 32 wt % chloride salt with a counter ion A.sup.+a with 2≤a, from about 1 wt % to about 10 wt % particulate polyethylene glycol having an average molecular weight from about 1600 g/mol to about 50,000 g/mol, and from about 10 wt % to about 50 wt % of the water soluble polymer that is not a polyether. The suspensions have chlorides in a sufficient amount to inhibit hydration of the suspended water soluble polymer and the particulate polyethylene glycol. The aqueous suspension can be formed by adding a powder of polyethylene glycol to a high salt solution and then adding the high molecular weight polymer. The aqueous suspensions can be useful as friction reducing agents in flowing liquids, such as for hydraulic fracture.

A method for producing a polycondensate melt from a primary material and a secondary material from materials of substantially the same type is provided. A first partial melt stream of the primary material and a second partial melt stream of the secondary material are provided, and a measured value of the intrinsic viscosity of both partial melt streams is determined, and a difference value is calculated from the measured values. Based on the difference value, the intrinsic viscosity of the second partial melt stream is increased, reduced or maintained unchangedly by using a first melt treatment device. Subsequently, the two partial melt streams are combined into a common melt stream.

Disclosed is a process for producing a thermoformable and/or embossable particle/polymer composite using a ground particulate biological substrate S of nutrient tissue and a polymer P, characterized in that (i) the substrate S and the polymer P are homogeneously mixed, then (ii) the substrate S/polymer P mixture is converted into a particle layer, and thereafter (iii) the resulting particle layer is densified at a temperature higher than or equal to the glass transition temperature of the polymer P [Tg.sup.P] to form a thermoformable and/or embossable particle/polymer composite,
where (a) the substrate S comprises extracted ground coffee beans; and (b) the polymer P is thermoplastic and has a Tg.sup.P≥20° C. measured according to DIN EN ISO 11357-2 (2013-09).

Furthermore, a process for the manufacturing of a particle/polymer molding, a particle/polymer molding and its use as an element in buildings or in furniture are disclosed.

A production method for a low molecular weight polymer suitable for a melt-blown non-woven fabric and a production device for melt-blown non-woven fabric, with which a high molecular weight polymer can be reduced in molecular weight by applying a shear force to the high molecular weight polymer without adding an additive. The low molecular weight polymer and the melt-blown non-woven fabric are produced using a continuous high shearing device that applies a shear force to the high molecular weight polymer serving as a raw material by rotation of a screw body to reduce the molecular weight of the high molecular weight polymer so as to obtain a low molecular weight polymer, and cools the low molecular weight polymer by passing the low molecular weight polymer through a passage arranged in the axial direction inside the screw body.

The present invention relates to a cross-linkable polyolefin composition comprising a first olefin polymer (A) comprising a first comonomer comprising epoxy groups, and a second olefin polymer (B) comprising a second comonomer comprising carboxylic acid groups and/or precursor thereof.