Abstract: The present invention relates to a VOC reduction system and a VOC reduction method that applies pulse type thermal energy to a catalyst to activate the catalyst and oxidizes and removes the VOC.

Abstract: The present invention relates to a VOC reduction system and a VOC reduction method that applies pulse type thermal energy to a catalyst to activate the catalyst and oxidizes and removes the VOC.

Abstract: An object of the present invention is to provide a heating carrier that does not heat all of exhaust gas flowing into a catalyst converter, but directly supplies, to a catalyst layer, thermal energy in the form of an instantaneous pulse to effectively activate a catalyst during a cold start-up period, and thus may reduce emission pollutants with a small amount of energy, and an exhaust gas reduction carrier having the heating carrier. In order to accomplish the object, the heating carrier of the present invention may include a main body of which the inside is formed to have a honeycomb structure, the main body being formed of a conductive ceramic material that is a nonmetallic heating element; and a catalyst layer formed by coating a first catalyst on a surface of the main body.

Abstract: The present invention relates to a monolith catalyst for carbon-dioxide/methane reforming and a method of manufacturing the same, and more particularly to a novel monolith catalyst for a reforming reaction having improved thermal durability, configured such that a sintering inhibiting layer is formed by coating the surface of a monolith support with at least one element selected from the group consisting of Group 2, 3, 6, 13, 15 and 16 elements among elements in Period 3 or higher and an active catalyst layer is formed on the sintering inhibiting layer, thereby preventing carbon deposition and catalyst deactivation due to deterioration even upon reaction at high temperatures.

Abstract: The present invention relates to a method of directly preparing a dicarbamate compound from a diamine compound, and more particularly to a method of directly preparing a dicarbamate compound by reacting a diamine compound with an alcohol compound in the presence of a mixed gas of carbon monoxide (CO) and oxygen (O2) using a Pd/MOx catalyst configured such that a palladium (Pd) active metal is supported on a metal oxide or metalloid oxide carrier.

Abstract: An object of the present invention is to increase the reduction performance of nitrogen oxides compared to existing three-way catalysts; simultaneously inhibit the emission of ammonia and nitrous oxide; simplify a process by means of a method of further doping an iridium-ruthenium catalyst into a commercial three-way catalyst; and expand the scope of application. The present invention provides a catalyst for simultaneously inhibiting the emission of ammonia and nitrous oxide by doping an iridium-ruthenium catalyst component into a three-way catalyst (TWC), a diesel oxidation catalyst, or a lean NOx trap supported on a honeycomb support.

Abstract: The present invention relates to a VOC reduction system and a VOC reduction method that applies pulse type thermal energy to a catalyst to activate the catalyst and oxidizes and removes the VOC.

Abstract: Proposed are a naphthalene-based hydrogen storage material including a naphthalene group, the naphthalene-based hydrogen storage material being capable of being used as a hydrogen storage media for supplying hydrogen to a device using hydrogen such as a fuel cell and a hydrogen combustion device, and to a method of storing and releasing hydrogen using the same. The hydrogen storage material can exhibit a significantly high hydrogen capacity, and can have excellent cost competitiveness with the use of a low-cost organic compound which is commercially available in the art.

Abstract: Proposed is a carbon dioxide reforming (CDR) reactor having a multilayered catalyst layer arrangement for preventing catalyst deactivation, wherein, in the reactor in which a CDR reaction for reacting methane (CH4) with carbon dioxide (CO2) to reform the methane into a synthesis gas including carbon monoxide (CO) and hydrogen (H2) is performed, in order to prevent a case where an endothermic reaction between a catalyst and heated reactant gas supplied to the reactor gradually causes the temperature of the reactant gas to decrease and the catalyst is deactivated by cokes generated due to the decrease in temperature of the reactant gas, CDR catalysts in the reactor are arranged in multiple layers in a multilayered structure to allow the reactant gas temperature that has decreased due to the endothermic reaction to be restored in spaces between the catalyst layers.

Abstract: The present invention relates to a method of directly preparing a dicarbamate compound from a diamine compound, and more particularly to a method of directly preparing a dicarbamate compound by reacting a diamine compound with an alcohol compound in the presence of a mixed gas of carbon monoxide (CO) and oxygen (O2) using a Pd/MOx catalyst configured such that a palladium (Pd) active metal is supported on a metal oxide or metalloid oxide carrier.

Abstract: A manufacturing method thereof, and the catalyst for removing the nitrogen oxide includes a powdery gamma alumina support on which at least one selected from a group of titanium (Ti), lanthanum (La), or zirconium (Zr) is supported, wherein the support may be further supported with iridium (Ir) and ruthenium (Ru).

Abstract: The present invention relates to a monolith catalyst for carbon-dioxide/methane reforming and a method of manufacturing the same, and more particularly to a novel monolith catalyst for a reforming reaction having improved thermal durability, configured such that a sintering inhibiting layer is formed by coating the surface of a monolith support with at least one element selected from the group consisting of Group 2, 3, 6, 13, 15 and 16 elements among elements in Period 3 or higher and an active catalyst layer is formed on the sintering inhibiting layer, thereby preventing carbon deposition and catalyst deactivation due to deterioration even upon reaction at high temperatures.

Abstract: The present invention provides a solid-phase catalyst for decomposing hydrogen peroxide comprising a permanganate salt and a manganese (II) salt. The solid-phase catalyst stays a solid state in the form of nanoparticles at the time of hydrogen peroxide decomposition, and thus can be recovered for reuse and also has an excellent decomposition rate. In the method for producing a solid-phase catalyst for decomposing hydrogen peroxide according to the present invention, a solid-phase catalyst is produced from a solution containing a permanganate salt, a manganese (II) salt, and an organic acid, so that the produced solid-phase catalyst is precipitated as a solid component even after a catalytic reaction, and thus is reusable and environmentally friendly, and cost reduction can be achieved through the simplification of a catalyst production technique.

Abstract: The present invention relates to a Ru—Pd bimetallic catalyst for use in hydrogenation of a compound, and more particularly to a catalyst prepared by loading both ruthenium and palladium on a g-C3N4 support and to a selective hydrogenation process of a pyridine group in a reaction system containing both a pyridine group and a benzene group using the catalyst.

Abstract: This invention relates to a heterogeneous catalyst represented by Rh/C3N4 configured such that a complex of a rhodium compound and 3-benzoylpyridine is immobilized on a carbon nitride support.

Abstract: The present invention relates to a Ru—Pd bimetallic catalyst for use in hydrogenation of a compound, and more particularly to a catalyst prepared by loading both ruthenium and palladium on a g-C3N4 support and to a selective hydrogenation process of a pyridine group in a reaction system containing both a pyridine group and a benzene group using the catalyst.

Abstract: This invention relates to a catalyst used in a carbonylation of methanol using carbon monoxide to acetic acid, and more particularly to a heterogeneous catalyst represented by Rh/WxC (where x is an integer of 1 or 2) in which a complex of a rhodium compound and 3-benzoylpyridine is fixed on a support of tungsten carbide.

Abstract: A carbon dioxide conversion system is provided. The carbon dioxide conversion system includes: an ion transfer membrane that separates oxygen in the air; an oxy-fuel combustor that combusts using oxygen that is separated at the ion transfer membrane as an oxidizing agent; and a dry-reformer that converts carbon dioxide that is generated through an oxy-fuel combustion reaction of the oxy-fuel combustor and methane gas that is supplied from the outside to carbon monoxide and hydrogen by a dry-reforming reaction.

Abstract: The present invention provides a solid-phase catalyst for decomposing hydrogen peroxide comprising a permanganate salt and a manganese (II) salt. The solid-phase catalyst stays a solid state in the form of nanoparticles at the time of hydrogen peroxide decomposition, and thus can be recovered for reuse and also has an excellent decomposition rate. In the method for producing a solid-phase catalyst for decomposing hydrogen peroxide according to the present invention, a solid-phase catalyst is produced from a solution containing a permanganate salt, a manganese (II) salt, and an organic acid, so that the produced solid-phase catalyst is precipitated as a solid component even after a catalytic reaction, and thus is reusable and environmentally friendly, and cost reduction can be achieved through the simplification of a catalyst production technique.

Abstract: A carbon nitride heterogeneous catalyst containing rhodium, a method for preparing the catalyst, and a method for preparing acetic acid using the catalyst is disclosed. The heterogeneous catalyst is characterized in that the rhodium metal is contained in carbon nitride which is a support insoluble in a liquid solvent, such as water or alcohol. Thus, the catalyst can easily be separated from a resulting product even by a simple process such as filtration. Accordingly, the carbon nitride heterogeneous catalyst exhibits excellent long-term stability and activity by being capable of overcoming the disadvantages of the method using a conventional homogeneous catalyst and minimizing the phenomenon of rhodium leaching, compared to the results of the conventional homogeneous catalytic reactions. The catalyst can thus be effectively used for the preparation of acetic acid by a carbonylation reaction between methanol and carbon monoxide.