A method of manufacturing a flexible intrinsically antimicrobial absorbent porosic composite controlling for an effective pore size using removable pore-forming substances and physically incorporated, non-leaching antimicrobials. A flexible intrinsically antimicrobial absorbent porosic composite controlled for an effective pore size composited physically incorporated, high-surface area, non-leaching antimicrobials, optionally in which the physically incorporated non-leaching antimicrobial exposes nanopillars on its surface to enhance antimicrobial activity. A kit that enhances the effectiveness of the intrinsically antimicrobial absorbent porosic composite by storing the composite within an antimicrobial container.

High-density polyethylene mixed resin particles used as seed particles during seed polymerization, wherein said seed particles contain a mixed resin of 100 parts by weight of high-density polyethylene and 20 to 100 parts by weight of an ethylene copolymer; said high-density polyethylene has a density of 935 to 960 kg/m.sup.3 and a softening temperature of 115 to 130 C.; said ethylene copolymer is a copolymer of an ester-based monomer selected from an acrylic acid alkyl ester and an aliphatic saturated monocarboxylic acid vinyl, and etylene, contains 1 to 20% by weight of an ester-based monomer-derived component, and has a softening temperature of 75 to 110 C.; said acrylic acid alkyl ester is selected from methyl acrylate and ethyl acrylate; and said aliphatic saturated monocarboxylic acid vinyl is selected from vinyl acetate and vinyl propionate.

Disclosed herein is a highly flame retardant polyurethane spray foam composition. The composition includes 100 parts by weight to 200 parts by weight an isocyanate compound relative to 100 parts by weight of a resin mixture including 46 wt % to 75 wt % of a polyol, 10 wt % to 30 wt % of a blowing agent, and 5 wt % to 30 wt % of an additive, wherein the polyol includes 1 wt % to 10 wt % of a polyether polyol and 45 wt % to 65 wt % of an aromatic polyester polyol, and the aromatic polyester polyol has an average hydroxyl value of 250 mgKOH/g to 380 mgKOH/g.

The present invention relates to a process for the production of a geopolymer composite. It further relates to a geopolymer composite, and the use of a geopolymer, a geopolymer in combination with an athermanous additive, or the geopolymer composite in expanded vinyl polymer, preferably vinyl aromatic polymer. Furthermore, the invention relates to a process for the production of expandable vinyl aromatic polymer granulate, and expandable vinyl aromatic polymer granulate. Finally, the present invention relates to expanded vinyl foam, preferably vinyl aromatic polymer, and to a masterbatch comprising vinyl polymer and a), b), or c).

The invention relates to an extrusion process for the production of expandable vinyl aromatic polymer granulate comprising mixing first and second additives with first and second polymer components, respectively, in dedicated mixers.

The invention provides a stabilising composition for polymeric materials, comprising: a. a first derivatised phenolic antioxidant; b. at least one secondary arylamine having the formula (I): NHRyRx wherein: the or each R, which may be the same or different, independently denotes an optionally substituted hydrocarbyl group; x and y are each independently from 0 to 5 provided that at least one of x and y is at least 1; and provided that at least one R is an optionally substituted hydrocarbyl group having at least 9 carbon atoms; and c. one or more antioxidant boosters independently selected from: i. a second derivatised phenolic antioxidant having lower steric hindrance than the first derivatised phenolic antioxidant; ii. a hindered amine; iii. an optionally substituted phenothiazine; and also the use of the stabilising composition for stabilising polyol and/or polyurethane; and a stabilised composition comprising a polyol and/or polyurethane and the aforementioned low emission and anti-scorch stabilising composition. ##STR00001##

A process for the production of a geopolymer composite. The disclosure further relates to a geopolymer composite, and the use of a geopolymer, a geopolymer in combination with an athermanous additive, or the geopolymer composite in expanded vinyl polymer, preferably vinyl aromatic polymer. Furthermore, the disclosure relates to a process for the production of expandable vinyl aromatic polymer granulate, and expandable vinyl aromatic polymer granulate. Finally, the disclosure relates to expanded vinyl foam, preferably vinyl aromatic polymer, and to a masterbatch comprising vinyl polymer and a), b), or c).

This present invention discloses a halogen-free flame retardant polyolefin foam composite, which is comprises: 80-125 parts by weight of ethylene/vinyl acetate copolymer (EVA), 8-13 parts by weight of high density polyethylene (HDPE) or low density polyethylene (LDPE), 15-25 parts by weight of polyolefin elastomer (POE), 60-77 parts by weight of acid source material, 17-22 parts by weight of carbon source material, 8-11 parts by weight of gas source material, 1-8 parts by weight of retardant synergist, 5.5-8 parts by weight of composite foaming agent, 0.7-1.0 parts by weight of crosslinking agent, 4.0-5.5 parts by weight of plasticizer, 0.5-1.6 parts by weight of surface treatment agent, 20-35 parts by weight of compatibility, 6-14 parts by weight of inorganic filler, and 1.6-4.6 parts by weight of additive. This halogen-free flame retardant polyolefin foam composite has the advantages of good softness, flexibility, impact resistance, low density, low compressibility and deformability, good shock absorbability, and so on.

Polymer extruded foams that contain cell size enlarging agents are provided. The inventive composition includes a foamable polymer material, at least one blowing agent, and at least one cell size enlarging agent. The blowing agent utilized in the inventive composition is preferably selected such that the composition has a zero ozone depletion and low global warming potential. Examples include any inorganic blowing agents and/or non-hydrogenated chlorofluorocarbons (non-HCFCs). The foamable polymer material is preferably polystyrene. The cell size enlarging agent may be chosen from ethylene vinyl acetate (EVA) and/or ethylene methyl acrylate (EMA). The cell size enlarging agent permits the formation of a foam with large cell sizes that are desirable to achieve a high insulation value and to optimize the physical properties of the foamed product. In addition, the cell size enlarging agent provides an increased cell size to the foamed product without detracting from the physical and thermal properties.

PLA polymers that can be expanded into microporous articles having a node and fibril microstructure are provided. The fibrils contain PLA polymer chains oriented with the fibril axis. Additionally, the PLA polymers have an inherent viscosity greater than about 3.8 dL/g and a calculated molecular weight greater than about 150,000 g/mol. The PLA polymer article may be formed by bulk polymerization where the PLA bulk polymer is made into a preform that is subsequently expanded at temperatures above the glass transition temperature and below the melting point of the PLA polymer. In an alternate embodiment, a PLA polymer powder is lubricated, the lubricated polymer is subjected to pressure and compression to form a preform, and the preform is expanded to form a microporous article. Both the preform and the microporous article are formed at temperatures above the glass transition temperature and below the melting point of the PLA polymer.