Abstract: The present invention relates to a reaction mixture for manufacturing an inorganic-filler based closed-cell rigid polyurethane or polyisocyanurate (PU or PIR) containing foam having a calorific value below 6 MJ/kg, preferably below 4.5 MJ/kg, more preferably below 3 MJ/kg, measured according to EN ISO 1716, the reaction mixture comprising: At least one polyisocyanate-containing compound; At least one isocyanate-reactive compound; An inorganic filler composition; At least one physical blowing agent; characterised in that said inorganic filler composition has bulk density higher than 2 g/cm3, preferably higher than 2.1 g/cm3, more preferably higher than 2.2 g/cm3, even more preferably higher than 2.4 g/cm3.

Abstract: A reactive composition for making a PIR comprising foam at an isocyanate index of at least 120, said composition comprising at least an isocyanate composition comprising one or more isocyanate compounds, an isocyanate-reactive composition comprising one or more isocyanate-reactive compounds, at least one PIR promoting catalyst, at least one physical blowing agent with a lambda gas ?12 mW/m·K at 10° C., at least one CO2 scavenging compound selected from at least one epoxy compound, and optionally a catalyst promoting epoxy reaction with CO2 characterized in that the amount of isocyanate-reactive compounds in the reactive composition is at least 10 wt % calculated on the total weight of the reactive composition, or at least more than the amount of epoxy compounds and the molar amount of epoxy compounds in the reactive composition is at least 7.8 times higher than the molar amount of CO2 formed by the water present in the reactive composition after reaction with isocyanates.

Abstract: Polyisocyanurate (PIR) and/or polyurethane (PUR) comprising insulation foams having significantly improved long term insulation values are disclosed as well as a processing method to fabricate said improved insulation foams and use of the improved insulation foams for thermal insulation.

Abstract: A (super)hydrophobic isocyanate based organic aerogel/xerogel/cryogel having a water contact angle of at least 90° comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, and hydrophobic compounds having before the gelling step at least one isocyanate-reactive group and no isocyanate groups Characterized in that said hydrophobic compounds are covalently bonded within the porous network of the aerogel/xerogel/cryogel and wherein said bondings are created during the gelling step of the formation of the isocyanate based organic aerogel/xerogel/cryogel cross-linked porous network structure.

Abstract: A reaction mixture and a process for making a polyisocyanurate comprising rigid foam having a density in the range 50-500 kg/m3 is disclosed, said process having a cream time >35 seconds and a snap cure behaviour.

Abstract: Polyisocyanurate (PIR) and/or polyurethane (PUR) comprising insulation foams having significantly improved long term insulation values are disclosed as well as a processing method to fabricate said improved insulation foams and use of the improved insulation foams for thermal insulation.

Abstract: Functionalized isocyanate based organic aerogel/xerogel/cryogel comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, comprising on their pore surface before functionalization reactive groups (B) and functionalization molecules having a solubility in water <10 g/L at 20° C. chemically attached to the pore surface of the cross-linked porous network structure wherein said molecules have at least one reactive group (A) being capable of binding to said pore surface (by reaction with groups (B)) and at least one functional group (C) providing the pore surface with the desired functionalization.

Abstract: A synthesis method for making an isocyanate based organic xerogel having a low density (i.e. <400 kg/m3) and a small pore size (<150 nm) in combination with a specific surface area >100 m2/g is disclosed. The synthesis method avoiding or reducing gel shrinkage during the solvent removal step is characterized by the step wherein the organic solvent used to synthesize the isocyanate based organic xerogel is replaced by water such that during the solvent removal step only water needs to be removed to dry the porous network and to obtain the isocyanate based organic xerogel.

Abstract: A reaction mixture and a process for making a polyisocyanurate comprising rigid foam having a density in the range 50-500 kg/m3 is disclosed, said process having a cream time >35 seconds and a snap cure behaviour.

Abstract: A (super)hydrophobic isocyanate based organic aerogel/xerogel/cryogel having a water contact angle of at least 90° comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, and hydrophobic compounds having before the gelling step at least one isocyanate-reactive group and no isocyanate groups Characterized in that said hydrophobic compounds are covalently bonded within the porous network of the aerogel/xerogel/cryogel and wherein said bondings are created during the gelling step of the formation of the isocyanate based organic aerogel/xerogel/cryogel cross-linked porous network structure.

Abstract: A synthesis method for making an isocyanate based organic xerogel having a low density (i.e. <400 kg/m3) and a small pore size (<150 nm) in combination with a specific surface area >100 m2/g is disclosed. The synthesis method avoiding or reducing gel shrinkage during the solvent removal step is characterized by the step wherein the organic solvent used to synthesize the isocyanate based organic xerogel is replaced by water such that during the solvent removal step only water needs to be removed to dry the porous network and to obtain the isocyanate based organic xerogel.

Abstract: Functionalized isocyanate based organic aerogel/xerogel/cryogel comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, comprising on their pore surface before functionalization reactive groups (B) and functionalization molecules having a solubility in water <10 g/L at 20° C. chemically attached to the pore surface of the cross-linked porous network structure wherein said molecules have at least one reactive group (A) being capable of binding to said pore surface (by reaction with groups (B)) and at least one functional group (C) providing the pore surface with the desired functionalization.