The present invention provides stable amorphous calcium carbonate (ACC) compositions, and food articles comprising said compositions.

The present invention provides stable amorphous calcium carbonate (ACC) compositions, and food articles comprising said compositions.

Methods, systems, and apparatus, relate to a method for carbon capture from sea water. A first source of sea water into a reverse osmosis chamber. Reverse osmosis is performed on the sea water to produce fresh water and brine. The brine is provided to an electrolyzer. A current is passed through the brine and fresh water, thereby producing a hydroxide solution in a cathode chamber of the electrolyzer. The hydroxide solution is collected and placed into a contacting chamber and new sea water introduced. Precipitates are produced comprising at least calcium carbonate and magnesium carbonate.

Bauxite residue recovery includes mixing a solution of hydrochloric acid (HCL) according to a predetermined concentration, and adding the HCL solution to a quantity of raw red mud recovered from industrial operations as waste material. The highly alkaline property of the bauxite residue, commonly known as red mud is at least partially neutralized from the HCL, and makes the resulting washed red mud more amenable to subsequent uses in various applications in fields such as construction, wastewater treatment, and metal recovery processes. The process recovers washed red mud from the red mud and HCL solution by filtering the raw red mud and HCL solution for generating a stream of leach liquor from the filtrate and the recovered washed red mud from the residue. The neutralized red mud is further treated to extract metals such as calcium, iron, aluminum, silicon, and titanium.

The subject process relates generally to producing an aqueous solution through a simple but highly effective chemical reaction. The aqueous solution is composed of a blended solution with water and an added solubilizer for the chemical reaction. The results produce an ionic solid and an alkaline liquid solution which are useful commercial products, and various applications including but not limited to use as a CO.sub.2 capture solvent.

The subject process relates generally to producing an aqueous solution through a simple but highly effective chemical reaction. The aqueous solution is composed of a blended solution with water and an added solubilizer for the chemical reaction. The results produce an ionic solid and an alkaline liquid solution which are useful commercial products, and various applications including but not limited to use as a CO.sub.2 capture solvent.

A method is described of using a surface-reacted calcium carbonate as an extrusion aid for the production of a puffed polysaccharide-based material, excluding fibrillated cellulose-containing materials. In embodiments, the surface-reacted calcium carbonate is a reaction product of ground natural calcium carbonate (GNCC) or precipitated calcium carbonate (PCC) with carbon dioxide.

Provided herein are methods and systems to form calcium carbonate comprising vaterite, comprising dissolving lime in an aqueous base solution under one or more precipitation conditions to produce a precipitation material comprising calcium carbonate and a supernatant solution, wherein the calcium carbonate comprises vaterite.

The present invention provides a system and method to mineralize CO.sub.2 into peridotite rocks in a controlled and efficient manner removing carbon permanently from the atmosphere. Carbon dioxide sequestration into peridotite rocks happens naturally by means of natural weathering. However, this process is so slow and might take thousands of years to transform considerable amount of CO.sub.2 into carbonate rocks. The present invention, however, shortens the time of mineralization considerably in a controlled and quantifiable manner. This is typically done by injecting CO.sub.2 into peridotite rock formation and creating an efficient reaction pathways and conditions for the mineralization reaction to happen and therefore store CO.sub.2 by conversion into magnesite (MgCO.sub.3) and calcite (CaCO.sub.3).

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.