Abstract: Disclosed are a method of preparing carbon-dioxide-selective separation membranes by controlling calcination conditions including rapid thermal processing and separation membranes produced thereby. More particularly, disclosed are a method of preparing carbon-dioxide-selective separation membranes that can improve CO2 permselectivity, particularly, exhibit excellent CO2 permselectivity in the presence of water in the feed gas, by controlling the size of defects in the separation membranes using rapid thermal processing, separation membranes produced thereby, and a method of capturing and removing carbon dioxide using the separation membranes.

Abstract: The present invention relates to a method of fabricating an organic structure directing agent-free CHA type zeolite membrane and a membrane fabricated thereby, and more particularly to a method of fabricating a continuous CHA type zeolite membrane, which exhibits CO2/N2 and CO2/CH4 separation performances comparable with those of conventional membranes, in a cost-effective manner without a calcination process by hydrothermal synthesis using an alkali metal hydroxide without using an organic structure directing agent, and to a membrane fabricated thereby.

Abstract: The present invention relates to a method of fabricating an organic structure directing agent-free CHA type zeolite membrane and a membrane fabricated thereby, and more particularly to a method of fabricating a continuous CHA type zeolite membrane, which exhibits CO2/N2 and CO2/CH4 separation performances comparable with those of conventional membranes, in a cost-effective manner without a calcination process by hydrothermal synthesis using an alkali metal hydroxide without using an organic structure directing agent, and to a membrane fabricated thereby.

Abstract: A hydrocarbon removal system according an embodiment of the present invention includes: a first area including a first hydrocarbon adsorption catalyst having a first pore size; and a second area including a second hydrocarbon adsorption catalyst having a second pore size, wherein the first pore size may be smaller than the second pore size, the first hydrocarbon adsorption catalyst may include CHA zeolite, and the second hydrocarbon adsorption catalyst may include ZSM-5 zeolite.

Abstract: Disclosed are a MWW/DDR type gas separation membrane comprising at least one MWW type zeolite and at least one DDR type zeolite and a method for preparing the same. One of the MWW type zeolite and the DDR type zeolite is disposed on the other thereof, wherein at least one of the MWW type zeolite and the DDR type zeolite is epitaxially grown. In the gas separation membrane, the DDR type zeolite is epitaxially grown from the MWW type zeolite, or the MWW type zeolite is epitaxially grown from the DDR type zeolite. Thus, the MWW/DDR type gas separation membrane is synthesized using a structural continuity of the MWW type zeolite and the DDR type zeolite. Thus, the gas separation membrane has excellent separation efficiency.

Abstract: The present invention relates to a method of controlling a defect structure in a chabazite (CHA) zeolite membrane, the CHA zeolite membrane having a controlled defect structure by the method and a method of separating CO2, H2, or He and water from a mixture of water and an organic solvent using the CHA zeolite membrane, and more particularly, to a method of controlling a defect structure in a CHA zeolite membrane that improves the separation performance by reducing the amount and size of defects formed in the CHA membrane structure when removing organic-structure-directing agents in the membrane through calcination at a low temperature using ozone.

Abstract: The present invention relates to a method of controlling a defect structure in an MFI zeolite membrane and a method of separating xylene isomers using the MFI zeolite membrane produced by the method, and more particularly, to a method of controlling a defect structure in an MFI zeolite membrane that improves the performance of separating a xylene isomer by reducing the amount and size of defects formed in the MFI membrane structure when removing organic-structure-directing agents in the membrane through calcination at a low temperature using ozone.

Abstract: The present invention relates to a method of post-treating a zeolite membrane, comprising treating a defective zeolite membrane with a chemical material such as a dye molecule, which has a size larger than that of the pores of the zeolite membranes and smaller than defects in the membrane, thereby healing the defects in the membrane. The post-treatment method performs post-treatment of the zeolite membrane under mild conditions (room temperature and normal pressure), thereby selectively healing the defects in the zeolite membrane and improving the performance of the zeolite membrane. In addition, the method may provide a high-performance membrane having a high separation factor, particularly under dry conditions.

Abstract: Disclosed are a method of preparing a zeolite nanosheet and a zeolite nanosheet particle prepared thereby, and more particularly a method of preparing a zeolite nanosheet capable of preparing a monolayer zeolite nanosheet through a simple process of mixing a multilayer zeolite precursor with a swelling agent to swell the multilayer zeolite precursor and drying and calcining the multilayer zeolite precursor, wherein the monolayer zeolite nanosheet is useful to separate a catalyst or gas, and a zeolite nanosheet particle prepared thereby.

Abstract: Disclosed are a method of preparing a zeolite nanosheet and a zeolite nanosheet particle prepared thereby, and more particularly a method of preparing a zeolite nanosheet capable of preparing a monolayer zeolite nanosheet through a simple process of mixing a multilayer zeolite precursor with a swelling agent to swell the multilayer zeolite precursor and drying and calcining the multilayer zeolite precursor, wherein the monolayer zeolite nanosheet is useful to separate a catalyst or gas, and a zeolite nanosheet particle prepared thereby.

Abstract: Disclosed are a method of preparing carbon-dioxide-selective separation membranes by controlling calcination conditions including rapid thermal processing and separation membranes produced thereby. More particularly, disclosed are a method of preparing carbon-dioxide-selective separation membranes that can improve CO2 permselectivity, particularly, exhibit excellent CO2 permselectivity in the presence of water in the feed gas, by controlling the size of defects in the separation membranes using rapid thermal processing, separation membranes produced thereby, and a method of capturing and removing carbon dioxide using the separation membranes.

Abstract: The present invention relates to a hydrocarbon adsorbent with metal-impregnated zeolite particles having regular mesopores and a manufacturing method therefor. The hydrocarbon adsorbent includes a metal cation and a metal oxide that are impregnated in zeolite particles, in particular, the zeolite particles include regularly formed mesopores having a size of 2 to 10. By adjusting a Si/Al ratio and mesoporosity of the mesopores, a hydrocarbon adsorbent may have increased adsorption capacity for hydrocarbons in a cold-start section and can rapidly oxidize the hydrocarbon upon desorption thereof, thereby reducing the discharge of exhaust gas produced in automobiles and industries.

Abstract: A hydrocarbon adsorbent, according to one embodiment of the present invention, comprises a copper-containing ZSM-5 zeolite, wherein a Si/Al molar ratio of the ZSM-5 zeolite may be 11.5 to 40, and the amount of the copper included is 1 wt % to 10 wt %.

Abstract: A hydrocarbon adsorbent, according to one embodiment of the present invention, comprises a copper-containing ZSM-5 zeolite, wherein a Si/Al molar ratio of the ZSM-5 zeolite may be 11.5 to 40, and the amount of the copper included is 1 wt % to 10 wt %.

Abstract: Disclosed are a heterogeneous zeolite membrane and a method of preparing the same, and more particularly a heterogeneous zeolite membrane that has CHA and DDR zeolite structures by growing seed particles into a crystal structure different from that of the zeolite membrane and can thus separate CO2/N2 and CO2/CH4 even under wet conditions, a method of preparing the same, and a method of capturing and removing carbon dioxide using the membrane.

Abstract: The present invention relates to a chabazite zeolite membrane with a controlled pore size and a production method thereof, wherein the sizes of pore space and pore mouth of the chabazite zeolite membrane are finely controlled through chemical vapor deposition. Through the chemical vapor deposition, defects present in the chabazite zeolite membrane are eliminated, and the pore size is effectively controlled. Thus, unlike hydrophilic membranes showing excellent CO2/N2 separation performance under a dry condition, the chabazite zeolite membrane with a controlled pore size according to the present invention has a hydrophobic surface, and thus can maintain excellent CO2/N2 separation performance even under a wet condition. Accordingly, the chabazite zeolite membrane of the present invention can effectively capture carbon dioxide from nitrogen under various environmental conditions.

Abstract: Disclosed are a CHA zeolite membrane and a method of preparing the same, and more particularly, a CHA zeolite membrane having high capacity to separate CO2/N2 and CO2/CH4 even under wet conditions using a membrane produced using a synthetic precursor having a controlled ratio of Si and Al, a method of preparing the same, and a method of capturing and removing carbon dioxide using the membrane.

Abstract: The present invention relates to a method of preparing a perm-selective porous membrane and a method of separating gases using the prepared porous membrane. According to the present invention, a membrane is synthesized using a hierarchically structured alumina porous support by a counter diffusion method. During this synthesis, the diffusion rate of metal ions loaded on the porous support is controlled by controlling the pore size of the porous support, and the position at which the membrane is synthesized is controlled by synthesizing the membrane inside the support. This can increase the physical stability of the membrane and make the membrane thicker so as to ensure higher H2/CO2 separation factors.

Abstract: Provided are a mobile terminal and a control method therefor. The mobile terminal includes: a touchscreen disposed on one side of a main body of the terminal; a push key mounted on the main body to receive a push input; and a controller that displays virtual keys associated with the settings or control of the terminal on the touchscreen when the push key is pushed, and executes functions associated with a speech recognition mode when a set period of time elapses without at least one touch input on the virtual keys being sensed.

Abstract: The present invention relates to a method of preparing a decadodecasil 3R (DDR) type zeolite membrane and a membrane prepared thereby, and more particularly, to a method of preparing a hydrophobic decadodecasil 3R (DDR) type zeolite membrane having a continuous out-of-plane orientation by adding a substrate on which a seed layer is formed to a silica source synthetic precursor containing a methyltropinium salt and performing a hydrothermal synthesis, and a method of capturing and removing carbon dioxide using a membrane prepared thereby.