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.

Divalent ions are extracted from solids by leaching to form a divalent ion-containing solution. The divalent ion-containing solution is subjected to concentration to form a concentrated divalent ion-containing solution. Precipitation of a divalent ion hydroxide salt is induced from the concentrated divalent ion-containing solution. In other cases, the concentrated divalent ion-containing solution is exposed to carbon dioxide to induce precipitation of a divalent ion carbonate salt.

Nanoparticles of calcium hydroxide having a dumbbell shape, wherein the dumbbell shape has rounded ends separated by a narrow central portion, wherein a ratio of a largest width of the central portion to a largest width of the rounded ends is 0.30 to 0.75, a length is in the range of 500 nm to 1100 nm, the largest width of the narrow central portion is 100 to 250 nm, and the largest width of the narrow central portion is 100 to 250 nm. The nanoparticles have a mesoporous structure and are made up of subparticles that have a size of 5 to 75 nm. A method of making the nanoparticles from calcined calcium carbonate sources is disclosed. Also disclosed is an enhanced fuel containing the nanoparticles.

Nanoparticles of calcium hydroxide having a dumbbell shape, wherein the dumbbell shape has rounded ends separated by a narrow central portion, wherein a ratio of a largest width of the central portion to a largest width of the rounded ends is 0.30 to 0.75, a length is in the range of 500 nm to 1100 nm, the largest width of the narrow central portion is 100 to 250 nm, and the largest width of the narrow central portion is 100 to 250 nm. The nanoparticles have a mesoporous structure and are made up of subparticles that have a size of 5 to 75 nm. A method of making the nanoparticles from calcined calcium carbonate sources is disclosed. Also disclosed is an enhanced fuel containing the nanoparticles.

A dielectric powder includes a core-shell structure including a core region formed in an inner portion thereof and a shell region covering the core region. The core region includes barium titanate (BaTiO.sub.3) doped with a metal oxide, and the shell region is formed of a ferroelectric material.

A dielectric powder includes a core-shell structure including a core region formed in an inner portion thereof and a shell region covering the core region. The core region includes barium titanate (BaTiO.sub.3) doped with a metal oxide, and the shell region is formed of a ferroelectric material.

Provided are a method of preparing a metal oxide-silica composite aerogel, and a metal oxide-silica composite aerogel having an excellent weight reduction property prepared by the method. The method includes a step of adding an acid catalyst to a first water glass solution to prepare an acidic water glass solution (step 1); a step of adding a metal ion solution to the acidic water glass solution to prepare a precursor solution (step 2); and a step of adding a second water glass solution to the precursor solution and performing a gelation reaction (step 3) to yield a metal oxide-silica composite wet gel, wherein, in steps 2 and 3, bubbling of an inert gas is performed during the adding of the metal ion solution or the second water glass solution, respectively.

A phosphor in which an element represented by R.sub. is solid-solutionized in a phosphor host crystal represented by M.sub.(L, A).sub.X.sub., wherein M is at least one type of element selected from Mg, Ca, Sr, Ba and Zn, L is at least one type of element selected from Li, Na and K, A is at least one type of element selected from Al, Ga, B, In, Sc, Y, La and Si, X is at least one type of element selected from O, N, F and Cl (where all of X being N is excluded), R is at least one type of element selected from Mn, Cr, Ti, Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho and Yb, , , and satisfy +++=9, 0.00<1.30, 3.704.30, 3.704.30, and 0.00<1.30.

A phosphor in which an element represented by R.sub. is solid-solutionized in a phosphor host crystal represented by M.sub.(L, A).sub.X.sub., wherein M is at least one type of element selected from Mg, Ca, Sr, Ba and Zn, L is at least one type of element selected from Li, Na and K, A is at least one type of element selected from Al, Ga, B, In, Sc, Y, La and Si, X is at least one type of element selected from O, N, F and Cl (where all of X being N is excluded), R is at least one type of element selected from Mn, Cr, Ti, Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho and Yb, , , and satisfy +++=9, 0.00<1.30, 3.704.30, 3.704.30, and 0.00<1.30.

Calcium hydroxide nanoparticles (Ca(OH).sub.2NPs) synthesized using carob pulp extract may be hexagonal nanoparticles with a diameter ranging from about 31.22 nm to about 81.22 nm. The Ca(OH).sub.2NPs may be synthesized by heating ethylene glycol, adding calcium hydroxide to the ethylene glycol to provide a first mixture, heating the first mixture, adding a carob pulp aqueous extract to the first mixture to form a second mixture, heating the second mixture, adding sodium hydroxide (NaOH) to the second mixture to form a third mixture, heating the third mixture, resting the third mixture at room temperature after heating, centrifuging the third mixture, collecting a colloid sediment, extracting any unwanted contaminants from the colloid sediment, and drying the colloid sediment to obtain Ca(OH).sub.2NPs.