A low carbon footprint material is used to decrease the carbon dioxide emission for production of a high carbon footprint substance. A method of forming composite materials comprises providing a first high carbon footprint substance; providing a carbon nanomaterial produced with a carbon-footprint of less than 10 unit weight of carbon dioxide (CO.sub.2) emission during production of 1 unit weight of the carbon nanomaterial; and forming a composite comprising the high carbon footprint substance and from 0.001 wt % to 25 wt % of the carbon nanomaterial, wherein the carbon nanomaterial is homogeneously dispersed in the composite to reduce the carbon dioxide emission for producing the composite material relative to the high carbon footprint substance.

Building materials and methods of making a building material are disclosed. An exemplary method includes receiving algae; and subjecting the algae to an oil extraction process, in order to produce vegetable oil. The method further includes producing synthetic fibers by processing the vegetable oil from the oil extraction process; and processing the synthetic fibers to produce a tension and pressure resistant material.

A catalyst fibrous structure having a catalyst metal carried on a fibrous structure, wherein (a) a Log differential micropore volume distribution curve thereof obtained by measurement using a mercury intrusion technique has a peak having a maximum micropore diameter in the range of from 0.1 μm to 100 μm; (b) a Log differential micropore volume at the peak is 0.5 mL/g or more; and (c) an amount of a catalyst metal compound and a binder carried per unit volume is 0.05 g/mL or more. A production method for producing a catalyst fibrous structure having: (1) mixing a catalyst metal compound or a catalyst precursor, and an inorganic binder and a solvent; (2) grinding the mixture to obtain a coating material of the catalyst metal compound or the catalyst precursor having a median particle diameter of 2 μm or less and a viscosity of from 10 mPa.Math.s to 200 mPa.Math.s; (3) impregnating a fibrous structure with the coating material to fill up voids of the fibrous structure with the coating material of the catalyst metal compound or the catalyst precursor; (4) heating and drying the fibrous structure, directly as it is, at a temperature not lower than the boiling point of the solvent; and (5) heating and calcination the dried fibrous structure at a temperature not lower than the dehydration temperature of the inorganic binder to obtain a catalyst fibrous structure.

A catalyst fibrous structure having a catalyst metal carried on a fibrous structure, wherein (a) a Log differential micropore volume distribution curve thereof obtained by measurement using a mercury intrusion technique has a peak having a maximum micropore diameter in the range of from 0.1 μm to 100 μm; (b) a Log differential micropore volume at the peak is 0.5 mL/g or more; and (c) an amount of a catalyst metal compound and a binder carried per unit volume is 0.05 g/mL or more. A production method for producing a catalyst fibrous structure having: (1) mixing a catalyst metal compound or a catalyst precursor, and an inorganic binder and a solvent; (2) grinding the mixture to obtain a coating material of the catalyst metal compound or the catalyst precursor having a median particle diameter of 2 μm or less and a viscosity of from 10 mPa.Math.s to 200 mPa.Math.s; (3) impregnating a fibrous structure with the coating material to fill up voids of the fibrous structure with the coating material of the catalyst metal compound or the catalyst precursor; (4) heating and drying the fibrous structure, directly as it is, at a temperature not lower than the boiling point of the solvent; and (5) heating and calcination the dried fibrous structure at a temperature not lower than the dehydration temperature of the inorganic binder to obtain a catalyst fibrous structure.

Corrosion-resistant refractory binder compositions may be formed with a calcium ion source, high-alumina refractory aluminosilicate pozzolan, and water. Any one or more of such components may individually be non-cementitious. Examples of high-alumina refractory aluminosilicate pozzolan include crushed firebrick; firebrick grog; and mixtures of silicate and any one or more of corundum, high-alumina ceramic, and bauxite; refractory mortar; fire clay; mullite; fused mullite; and combinations thereof, among others. A binder composition may be mixed with sufficient amount of water to form a slurry, which slurry may be introduced into a subterranean formation (e.g., via a wellbore penetrating the subterranean formation). A plurality of the non-cementitious components may react in the presence of water when exposed to suitable conditions so as to enable the binder composition to set. Such compositions, once set, may exhibit enhanced corrosion and/or heat resistance as compared to other binder compositions.

Corrosion-resistant refractory binder compositions may be formed with a calcium ion source, high-alumina refractory aluminosilicate pozzolan, and water. Any one or more of such components may individually be non-cementitious. Examples of high-alumina refractory aluminosilicate pozzolan include crushed firebrick; firebrick grog; and mixtures of silicate and any one or more of corundum, high-alumina ceramic, and bauxite; refractory mortar; fire clay; mullite; fused mullite; and combinations thereof, among others. A binder composition may be mixed with sufficient amount of water to form a slurry, which slurry may be introduced into a subterranean formation (e.g., via a wellbore penetrating the subterranean formation). A plurality of the non-cementitious components may react in the presence of water when exposed to suitable conditions so as to enable the binder composition to set. Such compositions, once set, may exhibit enhanced corrosion and/or heat resistance as compared to other binder compositions.

Provided herein are compositions, methods, and systems comprising vaterite and magnesium oxide.

Provided herein are compositions, methods, and systems comprising vaterite and magnesium oxide.

This application relates to making magnesium oxychloride boards. A magnesium oxychloride slurry is mixed by directing magnesium chloride, magnesium oxide, at least one phosphate, at least one inorganic salt, and water into a mixer and mixing these ingredients together to form a slurry. At least one filler is then mixed with the slurry. The slurry is directed to a mold. The mold is formed with the slurry to form a magnesium oxychloride board. The magnesium oxychloride board is then cured.

This application relates to making magnesium oxychloride boards. A magnesium oxychloride slurry is mixed by directing magnesium chloride, magnesium oxide, at least one phosphate, at least one inorganic salt, and water into a mixer and mixing these ingredients together to form a slurry. At least one filler is then mixed with the slurry. The slurry is directed to a mold. The mold is formed with the slurry to form a magnesium oxychloride board. The magnesium oxychloride board is then cured.