An aqueous suspension including 5 to 65 wt. % of calcium hydroxide, wherein at least 50 wt. % of the calcium hydroxide is present in the form of nanoparticles, and at least one compound for stabilizing the suspension. The aqueous suspension accelerates the setting of mineral binder compositions without adversely affecting the processing properties of the composition.

Process for manufacturing a milk of lime of great fineness comprising at least the steps of providing one lime compound and forming said milk of lime with a process water and said lime compound.

Process for manufacturing a milk of lime of great fineness comprising at least the steps of providing one lime compound and forming said milk of lime with a process water and said lime compound.

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 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.

The present invention relates to a method for producing a highly porous fine powdery slaked lime composition, comprising a fluidification step for forming said highly porous fine powdery slaked lime composition having an Alpine fluidity greater than 50% and which is carried out in a dryer/grinder chosen from the group consisting of a pin-type dryer/grinder, a cage-type dryer/grinder, an instantaneous dryer/disagglomerator and a combination of these until the powdery slaked lime composition has a non-solid residual-phase content of less than or equal to 3.5% by weight and greater than or equal to 0.3% by weight, as well as the product obtained therefrom.

The present invention relates to a method for producing a highly porous fine powdery slaked lime composition, comprising a fluidification step for forming said highly porous fine powdery slaked lime composition having an Alpine fluidity greater than 50% and which is carried out in a dryer/grinder chosen from the group consisting of a pin-type dryer/grinder, a cage-type dryer/grinder, an instantaneous dryer/disagglomerator and a combination of these until the powdery slaked lime composition has a non-solid residual-phase content of less than or equal to 3.5% by weight and greater than or equal to 0.3% by weight, as well as the product obtained therefrom.

An oxide ion conductor has a X.sub.3Z.sub.2(TO.sub.4).sub.3 structure, where X is a divalent metal element, Z is a trivalent metal element, and T is a tetravalent metal element, and has a composition expressed by (X.sub.1-xA.sub.x).sub.3(Z.sub.1-yB.sub.y).sub.2(T.sub.1-zC.sub.z).sub.3O.sub.12+ where the element X is Ca, Fe, Gd, Ba, Sr, Mn, and/or Mg, the element Z is Al, Cr, Fe, Mn, V, Ga, Co, Ni, Ru, Rh, and/or Ir, the element T is Si and/or Ge, an element A is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and/or Sr, an element B is Zn, Mn, Co, Ru, and/or Rh, and an element C is Si, Al, Ga, and/or Sn, 0x0.2, 0y0.2, and 0z0.2 are satisfied, and is a value securing electrical neutrality.

An oxide ion conductor has a X.sub.3Z.sub.2(TO.sub.4).sub.3 structure, where X is a divalent metal element, Z is a trivalent metal element, and T is a tetravalent metal element, and has a composition expressed by (X.sub.1-xA.sub.x).sub.3(Z.sub.1-yB.sub.y).sub.2(T.sub.1-zC.sub.z).sub.3O.sub.12+ where the element X is Ca, Fe, Gd, Ba, Sr, Mn, and/or Mg, the element Z is Al, Cr, Fe, Mn, V, Ga, Co, Ni, Ru, Rh, and/or Ir, the element T is Si and/or Ge, an element A is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and/or Sr, an element B is Zn, Mn, Co, Ru, and/or Rh, and an element C is Si, Al, Ga, and/or Sn, 0x0.2, 0y0.2, and 0z0.2 are satisfied, and is a value securing electrical neutrality.

A hydrated lime product exhibiting superior reactivity towards HCl and SO.sub.2 in air pollution control applications. Also disclosed is a method of providing highly reactive hydrated lime and the resultant lime hydrate where an initial lime feed comprising calcium and impurities is first ground to a particle-size distribution with relatively course particles. Smaller particles are then removed from this ground lime and the smaller particles are hydrated and flash dried to form a hydrated lime, which is then milled to a significantly smaller particle size than that of the relatively course particles. The resultant lime hydrate product has available CaOH of greater than 92%, a citric acid reactivity of less than 20 seconds, a BET surface area greater than 18, a D90 less than 10 m, a D50 less than 4 m, a D90/D50 less than 3, and a large pore volume of greater than 0.2 BJH.