A mineral wool product comprises mineral fibers bound by a binder resulting from the curing of a binder composition comprising a phenol-formaldehyde-based resin, and/or a carbohydrate containing component; a hydrophobic agent comprising (i) at least one silicone compound, such as silicone resin; (ii) at least one hardener, such as silane; (iii) optionally, at least one emulsifier; as insulation of a metallic structure, said structure having an operating temperature between 0-650° C.

A mineral wool product comprises mineral fibers bound by a binder resulting from the curing of a binder composition comprising a phenol-formaldehyde-based resin, and/or a carbohydrate containing component; a hydrophobic agent comprising (i) at least one silicone compound, such as silicone resin; (ii) at least one hardener, such as silane; (iii) optionally, at least one emulsifier; as insulation of a metallic structure, said structure having an operating temperature between 0-650° C.

A mineral wool product comprises mineral fibers bound by a binder resulting from the curing of a binder composition comprising a phenol-formaldehyde-based resin, and/or a carbohydrate containing component; a hydrophobic agent comprising (i) at least one silicone compound, such as silicone resin; (ii) at least one hardener, such as silane; (iii) optionally, at least one emulsifier; as insulation of a metallic structure, said structure having an operating temperature between 0-650° C.

The surface-treated glass cloth includes a surface treatment layer on a surface, and the surface treatment layer includes: a first silane coupling agent containing at least one amine selected from the group consisting of a primary amine, a secondary amine and a tertiary amine and containing no quaternary ammonium cation; a second silane coupling agent containing at least one quaternary ammonium cation; an organic acid; and a surfactant. A total content of the first silane coupling agent and the second silane coupling agent is 0.05 to 1.20 mass% based on the total amount of the surface-treated glass cloth, a ratio of a molar content of the first silane coupling agent to a molar content of the second silane coupling agent is 1.1 to 10.0, and a content of the organic acid is 50 to 300 ppm based on the total amount of the surface-treated glass cloth.

The surface-treated glass cloth includes a surface treatment layer on a surface, and the surface treatment layer includes: a first silane coupling agent containing at least one amine selected from the group consisting of a primary amine, a secondary amine and a tertiary amine and containing no quaternary ammonium cation; a second silane coupling agent containing at least one quaternary ammonium cation; an organic acid; and a surfactant. A total content of the first silane coupling agent and the second silane coupling agent is 0.05 to 1.20 mass% based on the total amount of the surface-treated glass cloth, a ratio of a molar content of the first silane coupling agent to a molar content of the second silane coupling agent is 1.1 to 10.0, and a content of the organic acid is 50 to 300 ppm based on the total amount of the surface-treated glass cloth.

A reinforcing material is disclosed that includes coated glass flakes and coated glass strands. When the total amount of a glycidyl group-including resin and aminosilane contained in the coatings of the coated glass flakes corresponds to 100% by mass, the amount of the resin is 30% to 95% by mass. When the total amount of a glycidyl group-including resin, aminosilane, and a urethane resin contained in the coatings of the coated glass strands corresponds to 100% by mass, the amount of the glycidyl group-including resin is 10% to 90% by mass, the amount of the aminosilane is 0.1% to 40% by mass, and the amount of the urethane resin is 1% to 50% by mass. Both the coated glass flakes and the coated glass strands have an ignition loss of 0.1% to 2.0% by mass measured pursuant to JIS R3420 (2013).

A reinforcing material is disclosed that includes coated glass flakes and coated glass strands. When the total amount of a glycidyl group-including resin and aminosilane contained in the coatings of the coated glass flakes corresponds to 100% by mass, the amount of the resin is 30% to 95% by mass. When the total amount of a glycidyl group-including resin, aminosilane, and a urethane resin contained in the coatings of the coated glass strands corresponds to 100% by mass, the amount of the glycidyl group-including resin is 10% to 90% by mass, the amount of the aminosilane is 0.1% to 40% by mass, and the amount of the urethane resin is 1% to 50% by mass. Both the coated glass flakes and the coated glass strands have an ignition loss of 0.1% to 2.0% by mass measured pursuant to JIS R3420 (2013).

The present invention relates to a fiber composite material and a method for producing the fiber composite material. The method for producing the fiber composite material includes a hydrolysis step of a silicon precursor having an alkoxy group, an in-situ condensation step and a drying step. A specific silicon precursor having a secondary amino group and alkyl groups is used therein, as well as a specific weight ratio of the silicon precursor to a fiber material, the in-situ condensation step can be performed in the absence of organic solvents in the method for producing the fiber composite material, and a hydrophobic modification on silicon-based gels can be performed, thereby simplifying the process, decreasing a thermal conductivity of the resulted fiber composite material and preventing drop dust of the resulted fiber composite material.

The present invention relates to a fiber composite material and a method for producing the fiber composite material. The method for producing the fiber composite material includes a hydrolysis step of a silicon precursor having an alkoxy group, an in-situ condensation step and a drying step. A specific silicon precursor having a secondary amino group and alkyl groups is used therein, as well as a specific weight ratio of the silicon precursor to a fiber material, the in-situ condensation step can be performed in the absence of organic solvents in the method for producing the fiber composite material, and a hydrophobic modification on silicon-based gels can be performed, thereby simplifying the process, decreasing a thermal conductivity of the resulted fiber composite material and preventing drop dust of the resulted fiber composite material.

The present invention concerns a sizing composition for glass fibers comprising the following components: (a) A silane based coupling agent which is not an aminosilane; (b) A film former; (c) A borate; (d) A lubricant Characterized in that, at least 75 wt. % of the silane coupling agent present in the composition is dialkoxylated. It also concerns a glass fiber sized with the reaction product of said sizing composition, as well as a polymeric composite reinforced with such glass fibers.