The present invention relates to a surface-reacted magnesium carbonate, a delivery system for the release of one or more active agent(s) in a home care formulation comprising the surface-reacted magnesium carbonate, a home care formulation comprising the delivery system for the release of one or more active agent(s), a method for preparing the surface-reacted magnesium carbonate and a method for preparing the delivery system for the release of one or more active agent(s) in a home care formulation, as well as the use of the surface-reacted magnesium carbonate as a carrier material for the release of one or more active agent(s) in a home care formulation and the use of the delivery system for the release of one or more active agent(s) in a home care formulation.

The present invention relates to a surface-reacted magnesium carbonate, a delivery system for the release of one or more active agent(s) in a home care formulation comprising the surface-reacted magnesium carbonate, a home care formulation comprising the delivery system for the release of one or more active agent(s), a method for preparing the surface-reacted magnesium carbonate and a method for preparing the delivery system for the release of one or more active agent(s) in a home care formulation, as well as the use of the surface-reacted magnesium carbonate as a carrier material for the release of one or more active agent(s) in a home care formulation and the use of the delivery system for the release of one or more active agent(s) in a home care formulation.

Methods for fabrication of and use of magnesium oxide sorbents for room temperature carbon dioxide adsorption are provided. In accordance with one aspect, a method for fabrication of sorbents is provided which includes using calcination to obtain MgO—Mg(OH).sub.2 nano-composites and aging the MgO—Mg(OH).sub.2 nano-composites to form nano MCHs for room temperature carbon dioxide adsorption. According to another aspect, a method for fabrication of sorbents which includes fabrication of monoclinic magnesium malate tetrahydrate (C.sub.8H.sub.10MgO.sub.10.4H.sub.2O) and use of such sorbents for room temperature carbon dioxide adsorption is provided.

Methods for fabrication of and use of magnesium oxide sorbents for room temperature carbon dioxide adsorption are provided. In accordance with one aspect, a method for fabrication of sorbents is provided which includes using calcination to obtain MgO—Mg(OH).sub.2 nano-composites and aging the MgO—Mg(OH).sub.2 nano-composites to form nano MCHs for room temperature carbon dioxide adsorption. According to another aspect, a method for fabrication of sorbents which includes fabrication of monoclinic magnesium malate tetrahydrate (C.sub.8H.sub.10MgO.sub.10.4H.sub.2O) and use of such sorbents for room temperature carbon dioxide adsorption is provided.

Methods of producing solid CO.sub.2 sequestering carbonate materials are provided. Aspects of the methods include introducing a divalent cation source into a flowing aqueous liquid (e.g., a bicarbonate rich product containing liquid) under conditions sufficient such that a non-slurry solid phase CO.sub.2 sequestering carbonate material is produced. Also provided are systems configured for carrying out the methods.

Methods of producing solid CO.sub.2 sequestering carbonate materials are provided. Aspects of the methods include introducing a divalent cation source into a flowing aqueous liquid (e.g., a bicarbonate rich product containing liquid) under conditions sufficient such that a non-slurry solid phase CO.sub.2 sequestering carbonate material is produced. Also provided are systems configured for carrying out the methods.

The present invention relates to a particulate highly porous amorphous mesoporous magnesium carbonate material suitable for uptake of high amounts of oily substances, sebum or a beneficial agent or combinations of these and to topical and cosmetic compositions comprising such material. The particulate highly porous amorphous mesoporous magnesium carbonate material according to the invention has a total pore volume larger than 0.1 cm 3/g and is constituted of particles having a peak particle size at or below 35 μm.

The present invention relates to a particulate highly porous amorphous mesoporous magnesium carbonate material suitable for uptake of high amounts of oily substances, sebum or a beneficial agent or combinations of these and to topical and cosmetic compositions comprising such material. The particulate highly porous amorphous mesoporous magnesium carbonate material according to the invention has a total pore volume larger than 0.1 cm 3/g and is constituted of particles having a peak particle size at or below 35 μm.

To produce a calcium carbonate in a controlled form while carbon dioxide gas is efficiently used. A method for producing a calcium carbonate comprises a carbon dioxide gas absorption step of allowing an aqueous sodium hydroxide solution at a concentration of 5 to 21% to absorb carbon dioxide gas to give an aqueous sodium carbonate solution at a concentration of 4 to 24%; a hydration step of reacting calcium oxide with an aqueous sodium hydroxide solution at a concentration of 0 to less than 6% to give a lime milk that is a suspension of calcium hydroxide having a BET specific surface area of 5 to 40 m.sup.2/g; and a carbonation step of adding the aqueous sodium carbonate solution to the lime milk and performing reaction.

Systems and methods for sequestering carbon, evolving hydrogen gas, producing iron oxide as magnetite, and producing magnesium carbonate as magnesite through sequential carbonation and serpentinization/hydration reactions involving processed olivine- and/or pyroxene-rich ores, as typically found in mafic and ultramafic igneous rock. Precious or scarce metals, such nickel, cobalt, chromium, rare earth elements, and others, may be concentrated in the remaining ore to facilitate their recovery from any gangue material.