An electrical insulating system and an associated insulated stator bar are provided. The electrical insulating system includes an electrically insulating mica paper and a fiber glass disposed on a first surface of the electrically insulating mica paper. The electrically insulating mica paper and the fiber glass are impregnated with a curable binder resin composition. The curable binder resin composition includes about 21 weight percent to about 73 weight percent of a solid or semi-solid epoxy resin having an epoxide functionality of about 2.5, about 0.8 weight percent to about 49 weight percent of a liquid epoxy resin having an epoxide functionality of about 2, about 4 weight percent to about 15 weight percent of a bisphenol A-formaldehyde novolac, a metal acetylacetonate catalyst, and about 2.5 weight percent to about 15 weight percent of a toughener selected from the group consisting of polyethersulfone, methylmethacrylate butadiene styrene, and a combination thereof.

A composition comprising a mixture of: (i) an aromatic polycarbonate; (ii) a graft copolymer including polyacrylonitrile; and, (iii) a non-crosslinked acrylic polymer having a weight average molecular weight (Mw) of less than or equal to 65,000 Daltons (Da).

The invention is directed to a process for producing a ABS composition comprising 30-80 wt.-% of copolymer A, 19.99-60 wt.-% of ABS-copolymer B, 0-40 wt.-% of polymer C and 0.01-20 wt.-% of additives D, having the steps: a) mixing the components A, B and D and optionally C, by using an extruder comprising: a first feeding zone FZ1, a preheating zone PZ, a mechanical dewatering zone DZ, in which component B is mechanically dewatered, and wherein: the mechanical dewatering zone DZ comprises at least one dewatering aperture, in particular for liquid water; in a second feeding zone FZ2, at least part of component A and optionally part of component D are fed, preferably in melt and/or solid form, to the ex-truder, in a degassing zone DG component A and/or component B are degassed, and b) removing the ABS molding composition from a discharge zone CZ of the extruder.

The invention relates to a method for producing styrene monomers by the depolymerisation of polystyrene in the presence of foreign polymers, such as polyolefins. Said method comprises the following steps: a) introducing a polymer composition (A) containing: I) 10 to 99.5% by weight, based on the polymer composition (A), of polystyrene (I); and II) 0.1 to 89.9% by weight of polyolefin (II); and/or III) 0.1 to 4.9% by weight of acrylonitrile-based polymer (III); and/or IV) 0.1 to 4.9% by weight of polyester (IV), into the reaction zone (R) of a pyrolysis reactor (P); b) thermal cracking the polystyrene contained in the polymer composition (A) in the reaction zone (R) of the pyrolysis reactor (P) at a temperature of between 400-1000 C., c) removing the product mixture (G) obtained from the reaction zone (R), d) cooling of the product mixture (G), and e) separating the styrene monomers from the further components.

The invention relates to a process for recovery of rubber-modified vinyl(co)polymer from a polycarbonate resin or an optionally shredded molded part made thereof and the use of the recovered rubber-modified vinyl(co)polymer for the production of molded parts as well as blend partner in polycarbonate blends. Further optional aspects are the recovery of aromatic and/or aliphatic diol and the use of this diol for the production of polycarbonates.

The invention relates to a method for producing compositions containing vinyl-aromatic copolymers that are obtained in an emulsion polymerization process and comprise production-related salt inclusions. Said compositions are characterized by improved surface quality following storage in a warm-humid environment and are therefore suitable for producing molded articles having a class A surface that remains flawless over time.

A composition comprising a mixture of: (i) an aromatic polycarbonate; (ii) a graft copolymer including polyacrylonitrile; and, (iii) a non-crosslinked acrylic polymer having a weight average molecular weight (Mw) of less than or equal to 65,000 Daltons (Da).

A glass fiber-reinforced thermoplastic polymer composition has a sheathed continuous multifilament strand including a core that extends in the longitudinal direction and a polymer sheath which intimately surrounds the core, wherein the core has an impregnated continuous multifilament strand having at least one continuous glass multifilament strand, wherein the at least one continuous glass multifilament strand is impregnated with an impregnating agent, the polymer sheath is a thermoplastic polymer composition including a thermoplastic polymer, wherein the thermoplastic polymer contains a polyester having a weight average molecular weight of 15,000 to 80,000 Daltons as measured by gel permeation chromatography (GPC) using polystyrene standard and as measured by differential scanning calorimetry with a heating rate of 20 C./minute on first heating according to ASTM D3418-08, at least one crystalline melting point (Tm) of 200 to 290 C.

A novel material for producing auxetic foams is disclosed. The material comprises a multiphase, multicomponent polymer foam with a filler polymer having a carefully selected glass transition temperature. Novel methods for producing auxetic foams from the material are also disclosed that consistently, reliably and quickly produce auxetic polyurethane foam at about room temperature (25 C.). This technology overcomes challenging issues in the large-scale production of auxetic PU foams, such as unfavorable heat-transmission problem and harmful organic solvents.

In an embodiment, a natural rubber-based ABStarget polymer blend includes natural rubber-based ABS powder combined with a set of target polymers (e.g., polycarbonate (PC)). A natural rubber-based ABS powder production process includes producing grafted natural rubber; and mixing the grafted natural rubber with a set of grafted polybutadiene rubbers. The set of grafted polybutadiene rubbers includes at least one grafted polybutadiene rubber having a particle size that is significantly different than the grafted natural rubber particle size. In an embodiment, the grafted natural rubber exhibits a large particle size; a first grafted polybutadiene rubber exhibits a small particle size; and a second grafted polybutadiene rubber exhibits a medium particle size between the large and small particle sizes. Natural rubber-based ABStarget polymer blends in accordance with the present disclosure can exhibit generally equivalent or increased impact and/or tensile strength compared to other non-natural or synthetic rubber-based ABS blends.