A plaster treatment compound, in particular a compound for reinforcing waterproof plaster treatments containing water glass, which contains 20 to 69 wt % of an aqueous solution of potassium silicate, 20 to 59.9 wt % of aqueous lithium silicate solution, 10 to 20 wt % of octyltriethoxysilane, and 0.1 to 1 wt % water glass stabilizer.

A plaster treatment compound, in particular a compound for reinforcing waterproof plaster treatments containing water glass, which contains 20 to 69 wt % of an aqueous solution of potassium silicate, 20 to 59.9 wt % of aqueous lithium silicate solution, 10 to 20 wt % of octyltriethoxysilane, and 0.1 to 1 wt % water glass stabilizer.

Provided is a concrete hardener composition. The concrete hardener composition includes a sodium silicate compound, an acid compound and a balance amount of solvent. The sodium silicate compound includes sodium silicate or a mixture of sodium silicate and sodium methylsilicate. The acid compound includes acetic acid, glycolic acid, ethylenediaminetetraacetic acid, tartaric acid, nitric acid, boric acid or a combination thereof. The solvent includes water or a mixed solution of water and polyol. Based on the total weight of the concrete hardener composition, the content of silicon is between 5 wt % and 15 wt %, and the content of the acid compound is between 2 wt % and 30 wt %.

Provided is a concrete hardener composition. The concrete hardener composition includes a sodium silicate compound, an acid compound and a balance amount of solvent. The sodium silicate compound includes sodium silicate or a mixture of sodium silicate and sodium methylsilicate. The acid compound includes acetic acid, glycolic acid, ethylenediaminetetraacetic acid, tartaric acid, nitric acid, boric acid or a combination thereof. The solvent includes water or a mixed solution of water and polyol. Based on the total weight of the concrete hardener composition, the content of silicon is between 5 wt % and 15 wt %, and the content of the acid compound is between 2 wt % and 30 wt %.

A porous refractory in the K.sub.2O—SiO.sub.2—B.sub.2O.sub.3 system is formed by chemical direct foaming by heating to over 600° C., resulting in adherent black or white foam. The foam can function as highly porous thermal insulation, a high or low thermal emissivity surface, as a sealant for deteriorated refractory surfaces, as a filler for pockmarks/holes/gaps or as a bonding agent for parts with large gaps between them.

A porous refractory in the K.sub.2O—SiO.sub.2—B.sub.2O.sub.3 system is formed by chemical direct foaming by heating to over 600° C., resulting in adherent black or white foam. The foam can function as highly porous thermal insulation, a high or low thermal emissivity surface, as a sealant for deteriorated refractory surfaces, as a filler for pockmarks/holes/gaps or as a bonding agent for parts with large gaps between them.

A high-strength geopolymer hollow microsphere, a preparation method thereof and a phase change energy storage microsphere are provided, including: dissolving sodium hydroxide, sodium silicate and spheroidizing aid in water to form a solution A, and adding active powder to the solution A, stirring and uniformly mixing to form a slurry B, adding the slurry B to an oil phase, stirring and dispersing into balls, filtering to obtain geopolymer microspheres I, washing the geopolymer microspheres I, and then carrying out a high-temperature calcination to obtain the high-strength geopolymer hollow microspheres II; using the high-strength geopolymer hollow microsphere as a carrier, absorbing a phase change material into the carrier, and mixing a microsphere carrying the phase change material with an epoxy resin, adding a powder dispersant and stirring to disperse the microsphere, after the epoxy resin is solidified, screening the superfluous powder dispersant to obtain the phase energy storage microsphere.

A high-strength geopolymer hollow microsphere, a preparation method thereof and a phase change energy storage microsphere are provided, including: dissolving sodium hydroxide, sodium silicate and spheroidizing aid in water to form a solution A, and adding active powder to the solution A, stirring and uniformly mixing to form a slurry B, adding the slurry B to an oil phase, stirring and dispersing into balls, filtering to obtain geopolymer microspheres I, washing the geopolymer microspheres I, and then carrying out a high-temperature calcination to obtain the high-strength geopolymer hollow microspheres II; using the high-strength geopolymer hollow microsphere as a carrier, absorbing a phase change material into the carrier, and mixing a microsphere carrying the phase change material with an epoxy resin, adding a powder dispersant and stirring to disperse the microsphere, after the epoxy resin is solidified, screening the superfluous powder dispersant to obtain the phase energy storage microsphere.

Provided herein are methods and compositions utilizing one or more cementitious replacement materials, one or more alkaline activating materials, and, optionally one or more bonding materials and/or one or more setting time enhancer materials.

Provided herein are methods and compositions utilizing one or more cementitious replacement materials, one or more alkaline activating materials, and, optionally one or more bonding materials and/or one or more setting time enhancer materials.