Abstract: Process for improving the insulating capacity of expanded vinyl aromatic which includes: 1) preparing beads of expandable vinyl aromatic polymers containing 1-10% by weight, calculated with respect to the polymer, of an expanding agent englobed in the polymeric matrix, and 0.01-25% by weight, calculated with respect to the polymer, of an athermanous additive comprising carbon black homogeneously distributed in the polymeric matrix; 2) treating the surface of the beads, before deposition of the coating, with a liquid lubricating agent; and 3) thermally treating the beads with hot air at a temperature ranging from 30 to 60° C.

Abstract: Process for improving the insulating capacity of expanded vinyl aromatic which includes: 1) preparing beads of expandable vinyl aromatic polymers containing 1-10% by weight, calculated with respect to the polymer, of an expanding agent englobed in the polymeric matrix, and 0.01-25% by weight, calculated with respect to the polymer, of an athermanous additive comprising carbon black homogeneously distributed in the polymeric matrix; 2) treating the surface of the beads, before deposition of the coating, with a liquid lubricating agent; and 3) thermally treating the beads with hot air at a temperature ranging from 30 to 60° C.

Abstract: Process for improving the insulating capacity of expanded vinyl aromatic which comprises: 1) preparing beads of expandable vinyl aromatic polymers containing 1-10% by weight, calculated with respect to the polymer, of an expanding agent englobed in the polymeric matrix and 0.001-25% by weight, calculated with respect to the polymer (a), of an athermanous additive comprising carbon black homogeneously distributed in the polymeric matrix; 2) treating the surface of the beads, before deposition of the coating, with a liquid lubricating agent; and 3) thermally treating the beads with hot air at a temperature ranging from 30 to 60° C.

Abstract: Expandable vinylaromatic polymers which comprise: a) a matrix obtained by polymerizing 50-100% by weight of one or more vinylaromatic monomers and 0-50% by weight of a copolymerizable monomer; b) 1-10% by weight, calculated with respect to the polymer (a) of an expanding agent englobed in the polymeric matrix; c) 0.01-20% by weight, calculated with respect to the polymer (a) of carbon black distributed in the polymeric matrix having an average diameter ranging from 30 to 2000 nm, a surface area ranging from 5 to 40 m2/g, a sulfur content ranging from 0.1 to 2000 ppm and an ash content ranging from 0.001 to 1%.

Abstract: Process for improving the insulating capacity of expanded vinyl aromatic which comprises: 1) preparing beads of expandable vinyl aromatic polymers containing 1-10% by weight, calculated with respect to the polymer, of an expanding agent englobed in the polymeric matrix and 0.001-25% by weight, calculated with respect to the polymer (a), of an athermanous additive comprising carbon black homogeneously distributed in the polymeric matrix; 2) treating the surface of the beads, before deposition of the coating, with a liquid lubricating agent; and 3) thermally treating the beads with hot air at a temperature ranging from 30 to 60° C.

Abstract: Expandable vinylaromatic polymers which comprise: a) a matrix obtained by polymerizing 50-100% by weight of one or more vinylaromatic monomers and 0-50% by weight of a copolymerizable monomer; b) 1-10% by weight, calculated with respect to the polymer (a) of an expanding agent englobed in the polymeric matrix; c) 0.01-20% by weight, calculated with respect to the polymer (a) of carbon black distributed in the polymeric matrix having an average diameter ranging from 30 to 2000 nm, a surface area ranging from 5 to 40 m2/g, a sulfur content ranging from 0.1 to 2000 ppm and an ash content ranging from 0.001 to 1%.

Abstract: Process for the preparation of expandable vinylaromatic polymers which comprises: a) polymerizing in aqueous suspension at last one vinylaromatic monomer in the presence of a suspending agent selected from inorganic salts of phosphoric acid; b) recovering the expandable beads from the reaction container; c) washing the beads thus obtained with an aqueous solution containing 0.005-2% by weight of a non-ionic surface-active agent; d) recovering the washed beads substantially without any inorganic salt of phosphoric acid, on the surface, and drying them in a stream of air.