Abstract: The present invention relates to a novel titania photocatalyst and its manufacturing method. More specifically, the present invention is to provide the quantum-sized novel titania photocatalyst prepared the steps comprising: (a) titanium tetraisopropoxide is encapsulated in zeolite support by adding citric acid to isopropyl alcohol; (b) ethylene glycol is dissolved herein to obtain a uniformly dispersed mixture solution; and (c) it is encapsulated in zeolite cavities.

Abstract: The present invention provides a method for preparing a catalyst for the reduction of nitrogen oxides by the use of natural gas as a reducing agent in an excess oxygen atmosphere, which comprises of filling zeolite with an organic compound having molecular weight of 100˜250 prior to loading catalytically active noble metal components on a zeolite. Since the method according to the present invention supports catalytic active noble metal components on a zeolite under the condition that the pores of zeolite are filled with organic compounds, the noble metal component, which is essential for forming highly active NOx reduction catalyst, can be supported precisely on the desired positions of zeolite pores. Therefore, the NOx reduction catalysts prepared by the present invention are very useful for the purification of exhaust gas in an excessive oxygen atmosphere such as gas turbines, boilers or lean-burn automobiles.

Abstract: The present invention relates to a novel titania photocatalyst and its manufacturing method. More specifically, the present invention is to provide the quantum-sized novel titania photocatalyst prepared the steps comprising: (a) titanium tetraisopropoxide is encapsulated in zeolite support by adding citric acid to isopropyl alcohol; (b) ethylene glycol is dissolved herein to obtain a uniformly dispersed mixture solution; and (c) it is encapsulated in zeolite cavities.

Abstract: This invention relates to a continuous microwave synthesis process of inorganic materials and its apparatus and more particularly, to the process of synthesizing inorganic materials prepared in a manner such that after preparing a mixed solution of precursor materials for various inorganic materials such as porous molecular sieve, layered compounds and ceramics, this mixed solution is continuously added to a tube-type microwave reactor using a slurry pump for the synthesis and crystallization of inorganic materials.

Abstract: A process for preparing supported nickel catalyst consisting of supporting nickel or metal salt of nickel, alkali metal, alkaline earth metal having low melting point on silicon and aluminum-containing support having high surface area such as zeolite, silica and alumina as an oxide by melting effectively nickel or metal salt of nickel, alkali metal and alkaline earth metal having low melting point is disclosed. This process is characterized in that the supported nickel catalyst prepared by the present invention can be used in reforming reaction of hydrocarbons by using carbon dioxide, steam and oxygen as an oxidant. Metal salts used in the preparation of supported nickel catalyst is generally nitrate, chloride, acetate and carbonate having low melting point of 500° C. or less. The contents of nickel, alkali metal and alkaline earth metal of the catalyst are 1 to 20% by weight, 10% by weight or less and 20% by weight or less, respectively.

Abstract: The present invention relates to a process for preparing hydroxylated aromatics by using hydrogen and oxygen and more particularly, to a process for preparing hydroxylated aromatics by using hydrogen and oxygen with a two-component heterogeneous catalyst. One component consists of porous catalyst containing one of Group VIII B transition metals such as Pd, Pt, Au and Cu, and hydrogen transfer organic compounds such as anthraquinone. The other component consists of a catalyst containing a transition metal selected from Ti, V, and Sn with tetrahedral coordination geometry. The main advantages of this new catalytic system are to 1) overcome the drawbacks of liquid phase oxidation using conventional homogeneous catalysts, 2) avoid use of expensive hydrogen peroxide as an oxidant, and 3) improve the selectivity of the reaction.

Abstract: The invention herein relates to a catalyst for enhancing the conversion of the dehydrogenation reaction of aromatic hydrocarbons such as ethylbenzene under a flow of carbon dioxide, which is expressed by the following formula I, wherein a catalyst in which an active component of iron oxides is highly dispersed onto a zeolite, activated charcoal, .gamma.-alumina or silica carrier. Further, the invention relates to a dehydrogenation method of aromatic hydrocarbons by means of using said catalyst:(Fe.sup.II.sub.x Fe.sup.III.sub.y O.sub.z)/S (I)wherein S denotes a zeolite, activated charcoal, .gamma.-alumina or silica carrier, and the initial state of iron oxide is as follows:x=0.

Abstract: The invention herein relates to a catalyst for enhancing the conversion of the dehydrogenation reaction of aromatic hydrocarbons such as ethylbenzene under a flow of carbon dioxide, which is expressed by the following formula I, wherein a catalyst in which an active component of iron oxides is highly dispersed onto a zeolite, activated charcoal, .gamma.-alumina or silica carrier. Further, the invention relates to a dehydrogenation method of aromatic hydrocarbons by means of using said catalyst:(Fe.sup.II.sub.x Fe.sup.III.sub.y O.sub.z)/S (I)wherein S denotes a zeolite, activated charcoal, .gamma.-alumina or silica carrier, and the initial state of iron oxide is as follows:x=0.

Abstract: The invention herein relates to a direct manufacturing method of hydrogen peroxide over zeolite, wherein transition metals such as palladium or platinum, and organic compounds such as 2-alkyl anthraquinone or the like are encapsulated onto the zeolite channels, and then reducing agents such as hydrogen, ammonia or alcohol are used in the reaction temperature range of 10.about.90.degree. C. under atmospheric pressure. In general, alkyl anthiraquinone used in the conventional manufacturing, method of hydrogen peroxide can be easily hydrogenated in a relatively mild temperature condition in the range of room temperature to 100.degree. C. by means of a compound having hydrogen. However, the use of alkyl anthraquinone in the reaction is problematic due to the fact that it can only be utilized in a working solution with a solvent which can effectively dissolve alkyl anthraquinoe.

Abstract: The present invention provides a catalyst for reduction of nitrogen oxides represented by the formula (A.sub.a O.sub.x.B.sub.b O.sub.y).(C.sub.c O.sub.z.C'.sub.c' O.sub.z')/S which is produced by supporting mixed metal oxides represented by the formula (A.sub.z O.sub.x.B.sub.b O.sub.y).(C.sub.c O.sub.z.C'.sub.c' O.sub.z') in amorphous state on aluminum or silicon-containing support at calcination temperature of 400.degree. to 700.degree. C. in a molar ratio of 0.01:1 to 5:1, anda method for removing nitrogen oxides through selective catalytic reduction which comprises converting 50 to 50,000 ppm of nitrogen oxides in exhaust gas from automobile or from fixed source such as plant turbine and boiler, and other industry in a state of having 0.1 to 20% of excessive oxygen over (A.sub.a O.sub.x.B.sub.b O.sub.y).(C.sub.c O.sub.z.C'.sub.c' O.sub.z')/S catalyst by using 100 to 100,000 ppm of hydrocarbon reducing agent having 1 to 5 carbons under the reaction condition of 200.degree. to 800.degree. C.

Abstract: A process for producing a synthesis gas having carbon monoxide and hydrogen from the reduction of carbon dioxide with natural gas or lower hydrocarbons having methane as a main component and oxygen and steam over catalyst composed of nickel and, as promotors, alkali metal and alkaline earth metal component supported on silicon-containing support such as zeolite, silica, silicate and silica-alumina which are stable under reaction condition is disclosed. This process characterized in that the catalytic activity and performance property are improved by supporting alkali metal, alkaline earth metal and nickel oxide from metal salts having low melting point uniformly on silicon-containing support having high surface area by solid-state reaction. The amounts of adding alkali metal, alkaline earth metal and nickel are 0.01 to 10% by weight, 1 to 20% by weight and 1 to 20% by weight, respectively. The present invention is conducted in the temperature range from 600.degree. C. to 1000 .degree. C.