A method for the production of a cavity filled with a low-density mineral foam includes (i) preparing a cement slurry including Portland cement; ultrafine particles of which the D50 is from 10 to 600 nm; a water reducing agent; a manganese salt; and water; wherein the mass ratio of manganese salts/Portland cement is below 0.014; (ii) adding to the cement slurry obtained after (i) a gas-forming liquid including a gas-forming agent; and a viscosity-modifying agent which is a polymer chosen among anionic bio-based polymer, amphiphilic bio-based polymer, alkali swellable acrylic polymer and mixture thereof; to obtain a foaming slurry; (iii) filling the cavity with the foaming slurry obtained at (ii); (iv) leaving the foaming slurry to expand within the cavity.

A method for the production of a cavity filled with a low-density mineral foam includes (i) preparing a cement slurry including Portland cement; ultrafine particles of which the D50 is from 10 to 600 nm; a water reducing agent; a manganese salt; and water; wherein the mass ratio of manganese salts/Portland cement is below 0.014; (ii) adding to the cement slurry obtained after (i) a gas-forming liquid including a gas-forming agent; and a viscosity-modifying agent which is a polymer chosen among anionic bio-based polymer, amphiphilic bio-based polymer, alkali swellable acrylic polymer and mixture thereof; to obtain a foaming slurry; (iii) filling the cavity with the foaming slurry obtained at (ii); (iv) leaving the foaming slurry to expand within the cavity.

A method for the production of a cavity filled with a low-density mineral foam includes (i) preparing a cement slurry including Portland cement; ultrafine particles of which the D50 is from 10 to 600 nm; a water reducing agent; a manganese salt; and water; wherein the mass ratio of manganese salts/Portland cement is below 0.014; (ii) adding to the cement slurry obtained after (i) a gas-forming liquid including a gas-forming agent; and a viscosity-modifying agent which is a polymer chosen among anionic bio-based polymer, amphiphilic bio-based polymer, alkali swellable acrylic polymer and mixture thereof; to obtain a foaming slurry; (iii) filling the cavity with the foaming slurry obtained at (ii); (iv) leaving the foaming slurry to expand within the cavity.

A manufacturing process of a cement product includes: (1) incorporating at least one additive into a high-alumina cement composition, wherein the at least one additive is selected from nitrate-containing salts, nitrite-containing salts, carbonate-containing salts, sulfate-containing salts, chloride-containing salts, and hydroxide-containing salts; and (2) curing the high-alumina cement composition to form the cement product.

A manufacturing process of a cement product includes: (1) incorporating at least one additive into a high-alumina cement composition, wherein the at least one additive is selected from nitrate-containing salts, nitrite-containing salts, carbonate-containing salts, sulfate-containing salts, chloride-containing salts, and hydroxide-containing salts; and (2) curing the high-alumina cement composition to form the cement product.

A composition, utility material, and method of making a utility material is disclosed. A composition having an improved setting time may include a plurality of microparticles mixed with a sodium silicate binder and an isocyanate setting agent, where the microparticle composition has a setting time of less than or equal to one hour. A utility material may be a wallboard that includes the composition.

A composition for use in making a structural assembly board, a structural assembly made from the composition, and a method of making the structural assembly board is provided. The composition includes magnesium oxide having purity of 94-98 wt %; magnesium chloride; fly ash; and water. The magnesium oxide has at least two different particles sizes. The composition and method of making the structural assembly board promote formation of 5MgO.MgCl.sub.2.8H.sub.2O to improve structural qualities of the structural assembly board.

Methods of making permeable aerogels (100) can include providing a sol mixture (110) comprising an organic scaffold, an inorganic aerogel precursor, and a first solvent. The organic scaffold can be insoluble in the first solvent. The sol mixture can react to form a gel (120) such that an interconnected channel network is formed which is at least partially defined by the organic scaffold. The first solvent in the gel can be exchanged (130) with a second solvent. The second solvent can dissolve the organic scaffold to expose the interconnected channel network. The gel can be dried (140) to form the permeable aerogel.

Methods of making permeable aerogels (100) can include providing a sol mixture (110) comprising an organic scaffold, an inorganic aerogel precursor, and a first solvent. The organic scaffold can be insoluble in the first solvent. The sol mixture can react to form a gel (120) such that an interconnected channel network is formed which is at least partially defined by the organic scaffold. The first solvent in the gel can be exchanged (130) with a second solvent. The second solvent can dissolve the organic scaffold to expose the interconnected channel network. The gel can be dried (140) to form the permeable aerogel.

A cementitious composition with accelerated curing at low temperatures particularly at temperatures <5° C., especially at temperatures <0° C. The cementitious composition consists of 2 components with a first component A including at least one ordinary Portland cement, at least one cement selected from calcium aluminate cement and/or calcium sulfoaluminate cement, a powder P, selected from the group consisting of carbonates or hydrogen carbonates of alkali and/or alkaline earth metals, optionally aggregates, optionally other additives and a second component B comprising at least one accelerator, an anti-freeze agent, water, and optionally other additives. The composition shows increased development of compressive strength, maintain good workability, and have particularly low shrinkage, also when cured at temperatures <5° C., especially <0° C., and as low as −10° C.