C04B2/06

Method for the wet slaking of calcium and magnesium oxides from calcomagnesian compounds

A method is shown for the slaking of calcium oxides and magnesium from calcomagnesian compound containing at least 10 wt. % of MgO in relation to the total weight of said calcomagnesian compound, in which a slaking aqueous phase is supplied to a slaking device, and slaking the compound containing anhydrous dolomite delivered to the slaking device, by means of the slaking aqueous phase, forming hydrated solid particles of Mg(OH).sub.2, in the presence of an additive.

Method for the wet slaking of calcium and magnesium oxides from calcomagnesian compounds

A method is shown for the slaking of calcium oxides and magnesium from calcomagnesian compound containing at least 10 wt. % of MgO in relation to the total weight of said calcomagnesian compound, in which a slaking aqueous phase is supplied to a slaking device, and slaking the compound containing anhydrous dolomite delivered to the slaking device, by means of the slaking aqueous phase, forming hydrated solid particles of Mg(OH).sub.2, in the presence of an additive.

Method for the dry slaking of calcium and magnesium oxides from calcomagnesian compounds

The invention relates to a method for the dry slaking of calcium oxides and magnesium from calcomagnesian compound containing preferably at least 10 wt. % of MgO in relation to the total weight of said calcomagnesian compound, in which calcomagnesian compound is supplied to a slaking vessel, a slaking aqueous phase is supplied to the slaking vessel, followed by slaking the calcomagnesian compound delivered to the slaking vessel, by means of the slaking aqueous phase, and forming hydrated solid particles of calcium hydroxides and magnesium, in the presence of an additive. The invention also relates to the compound produced in this way.

Method for the dry slaking of calcium and magnesium oxides from calcomagnesian compounds

The invention relates to a method for the dry slaking of calcium oxides and magnesium from calcomagnesian compound containing preferably at least 10 wt. % of MgO in relation to the total weight of said calcomagnesian compound, in which calcomagnesian compound is supplied to a slaking vessel, a slaking aqueous phase is supplied to the slaking vessel, followed by slaking the calcomagnesian compound delivered to the slaking vessel, by means of the slaking aqueous phase, and forming hydrated solid particles of calcium hydroxides and magnesium, in the presence of an additive. The invention also relates to the compound produced in this way.

ENHANCED HYDRATE PRODUCED FROM FLASH CALCINED LIME AND METHODS OF MAKING THE SAME
20210387908 · 2021-12-16 ·

A system and related methods for the production of lime sorbent compositions from a calcium carbonate feedstock formed using flash calcination to produce the intermediate calcium oxide material.

HIGH TEMPERATURE HYDRATOR
20210380475 · 2021-12-09 ·

An apparatus includes a fluidized bed vessel with inlet ports arranged to receive at least one feed stream comprising calcium oxide, calcium carbonate, water, and a fluidizing gas into a fluidized bed vessel. The calcium oxide contacts the water to initiate a hydrating reaction to produce calcium hydroxide and heat. The fluidized bed vessel is configured to operate with a fluidization velocity that fluidizes and separates at least a portion of the calcium carbonate and at least a portion of the calcium oxide into a first fluidization regime, and at least a portion of the calcium hydroxide and at least another portion of the calcium oxide into a second fluidization regime. The apparatus further includes a heat transfer assembly configured to transfer heat of the hydrating reaction to the calcium carbonate, and a cyclone configured to separate a portion of the fluidization gas from a portion of at least one of the calcium hydroxide, calcium carbonate or calcium oxide.

Lime hydrate with improved reactivity via additives

Systems and Methods to produce a lime hydrate sorbent composition formed of highly reactive lime hydrate (HRH) by adding compounds to the slaking water in a method that would produce a non-HRH, which will typically be a lime hydrate having citric acid reactivity as discussed above of more than ten seconds, to make the non-HRH an HRH, which is having a citric acid reactivity of less than or equal to ten seconds.

Lime hydrate with improved reactivity via additives

Systems and Methods to produce a lime hydrate sorbent composition formed of highly reactive lime hydrate (HRH) by adding compounds to the slaking water in a method that would produce a non-HRH, which will typically be a lime hydrate having citric acid reactivity as discussed above of more than ten seconds, to make the non-HRH an HRH, which is having a citric acid reactivity of less than or equal to ten seconds.

Calcium hydroxide-containing compositions and associated systems and methods

Calcium hydroxide-containing compositions can be manufactured by slaking quicklime, and subsequently drying and milling the slaked product. The resulting calcium hydroxide-containing composition can have a size, steepness, pore volume, and/or other features that render the compositions suitable for treatment of exhaust gases and/or removal of contaminants. In some embodiments, the calcium hydroxide-containing compositions can include a D.sub.10 from about 0.5 microns to about 4 microns, a D.sub.90 less than about 30 microns, and a ratio of D.sub.90 to D.sub.10 less than 20, wherein individual particles include a surface area greater than or equal to about 25 m.sup.2/g.

Calcium hydroxide-containing compositions and associated systems and methods

Calcium hydroxide-containing compositions can be manufactured by slaking quicklime, and subsequently drying and milling the slaked product. The resulting calcium hydroxide-containing composition can have a size, steepness, pore volume, and/or other features that render the compositions suitable for treatment of exhaust gases and/or removal of contaminants. In some embodiments, the calcium hydroxide-containing compositions can include a D.sub.10 from about 0.5 microns to about 4 microns, a D.sub.90 less than about 30 microns, and a ratio of D.sub.90 to D.sub.10 less than 20, wherein individual particles include a surface area greater than or equal to about 25 m.sup.2/g.