Methods of making a bioactive glass fiber include forming a melt of a glass composition including: 50 to 70% SiO.sub.2; 0.1 to 10% Al.sub.2O.sub.3, 5 to 30% Na.sub.2O, 0.1 to 15% K.sub.2O, 0.1 to 15% MgO, 0.1 to 20% CaO, and 5 to 10% P.sub.2O.sub.5, based on a 100 wt % of the glass composition. The melt has a viscosity of from 200 Poise to 2,000 Poise. Methods include drawing the melt into a drawn glass fiber. Bioactive glass compositions include: 60 to 70% SiO.sub.2; 15 to 30% Na.sub.2O, 5 to 15% K.sub.2O, 1 to 10% CaO, and 5 to 10% P.sub.2O.sub.5, based on a 100 wt % of the glass composition.

A method of and an arrangement for recycling mineral wool waste to mineral wool production includes at least one melting furnace for melting virgin mineral wool raw material, the melting furnace including an inlet for virgin mineral wool raw material and an outlet for molten mineral wool material, a production line connected to the outlet for molten mineral wool material for producing a mineral wool product from the molten mineral wool material. The production line includes a curing oven, a fluidized bed reactor including an exhaust gas duct, an inlet for predetermined primary fuel, an inlet for predetermined bed material, and an outlet for an ash material, the ash material including bottom ash discharged via a bottom outlet from the fluidized bed reactor or fly ash separated by a particle separator from exhaust gas in the exhaust gas duct or a mixture of the bottom ash and the fly ash.

Dedust compositions suitable for use as dedust oil for mineral wool applications comprise a) from 95 percent by weight to 99.99 percent by weight of a triacyl glyceride sourced from a plant or animal oil, the triacyl glyceride having an IV of from 45 to 70, a viscosity at 30C of from 30 mPa.Math.s to 80 mPa.Math.s, and a Solid Fat Content of 15% w/w or less at 10C; and b) from 100 ppm to 2,500 ppm of an antioxidant. The dedust composition exhibits a flash point of at least 280C. In aspects, the dedust composition is liquid at 23C. In aspects, the triacyl glyceride is palm super olein.

Compatibilizing materials for use with fibers and polymeric compositions are described. A compatibilizing material can include a silane (Si) modified polyphenylene ether (PPE) oligomer having a resin reactive functional group. The resin reactive functional group can be between the PPE moiety and a Si moiety. In other instances, the resin reactive functional group can be a substituent of the Si moiety.

The present invention provides a binder for inorganic fibers characterized by containing (A) 100 parts by mass of a polyvinyl alcohol-based resin having a degree of polymerization of 100-3500, (B) 1-50 parts by mass of a metal salt, and (C) 3 parts by mass of an ammonia denatured product of a copolymerization product containing maleic anhydride. By using the binder for inorganic fibers according to the present invention, it is possible to produce an inorganic fiber mat having a high recovery rate comparable to that of phenol resins. In addition, the amount of volatile organic compounds released from such an inorganic fiber mat is extremely low.

A composition for producing a glass fiber, including the following components with corresponding percentage amounts by weight: SiO.sub.2: 57.4-60.9%; Al.sub.2O.sub.3: greater than 17% and less than or equal to 19.8%; MgO: greater than 9% and less than or equal to 12.8%; CaO: 6.4-11.8%; SrO: 0.1-1.5%; Na.sub.2O+K.sub.2O: 0.1-1.1%; Fe.sub.2O.sub.3: 0.05-1%; TiO.sub.2: lower than 0.8%; and SiO.sub.2+Al.sub.2O.sub.3: lower than or equal to 79.4%. The total weight percentage of the above components in the composition is greater than 99%. The weight percentage ratio of Al.sub.2O.sub.3+MgO to SiO.sub.2 is between 0.43 and 0.56, and the weight percentage ratio of CaO+MgO to SiO.sub.2+Al.sub.2O.sub.3 is greater than 0.205. The composition can significantly increase the glass modulus, effectively reduce the glass crystallization rate, secure a desirable temperature range (ΔT) for fiber formation and enhance the refinement of molten glass, thus making it particularly suitable for high performance glass fiber production with refractory-lined furnaces.

New glass compositions and applications thereof are disclosed. Embodiments of the present invention relate to glass compositions, to fiber glass strands, to chopped fiber glass strands, to nonwoven mats of glass fibers, and to other products and methods. A fiber glass strand comprises a plurality of glass fibers comprising the glass composition of the present invention.

A glass composition is provided that includes SiO.sub.2 in an amount from 50.0 to 65.0% by weight; Al.sub.2O.sub.3 in an amount from 18.0 to 23.0% by weight; CaO in an amount from 1 to 8.5% by weight; MgO in an amount from 9.0 to 14.0% by weight; Na.sub.2O in an amount from 0.0 to 1.0% by weight; K.sub.2O in an amount from 0.0 to 1.0% by weight; Li.sub.2O in an amount from 0.1 to 4.0% by weight; TiO.sub.2 in an amount from 0.0 to 2.5% by weight, Y.sub.2O.sub.3 in an amount from 0 to 10.0% by weight; La.sub.2O.sub.3 in an amount from 0 to 10.0% by weight; Ce.sub.2O.sub.3 in an amount from 0 to 5.0% by weight; and Sc.sub.2O.sub.3 in an amount from 0 to 5.0% by weight. Glass fibers formed from the inventive composition may be used in applications that require high stiffness and have elastic modulus between 88 and 115 GPa. Such applications include woven fabrics for use in forming wind turbine blades and aerospace structures.

A bioactive glass composition including: 50 to 70% SiO.sub.2; 0.1 to 10% Al.sub.2O.sub.3, 5 to 30% Na.sub.2O, 0.1 to 15% K.sub.2O, 0.1 to 15% MgO, 0.1 to 20% CaO, and 5 to 10% P.sub.2O.sub.5, based on a 100 wt % of the composition. Also disclosed is a method of making the bioactive glass composition.

An optical fiber draw system and method of coating an optical fiber. The system includes a furnace for heating an optical fiber preform, a draw assembly for drawing the optical fiber at a draw speed greater than 50 meters per second, a first coating applicator for applying a first coating onto the fiber, and a first curing assembly comprising a first plurality of light sources comprising light-emitting diodes for partially curing the first coating. The optical fiber draw system also includes a second coating applicator for applying a second coating onto the fiber on top of the first coating, and a second curing system comprising a second plurality of light sources for curing the second coating, wherein the first coating is further cured in the range of 15-50 percent after leaving the first curing assembly.