Abstract: Disclosed is a catalytic cracking process for the production of light olefins from a hydrocarbon feedstock using fast fluidization, which is a preferred process for more efficiently increasing the production of light olefin hydrocarbons. According to this invention, a fast fluidization regime is applied to a fluidized bed catalytic cracking process of producing light olefins using zeolite, such that a volume fraction and distribution of the catalyst sufficient to induce the catalytic cracking reaction can be provided, thus effectively enhancing the production of light olefin hydrocarbons, in particular, ethylene and propylene, at high selectivity.

Abstract: The present invention relates to a method for gasification of carbon-containing materials, and more specifically, to a method for gasification of carbon-containing materials which allows an increase in carbon efficiency and a reduction in carbon dioxide emission, comprising the steps of: gasification of carbon-containing materials to methane; thermal decomposition of CH4 to C and H2; and conversion of CO2 to CO using the carbon produced during the decomposition. The method of the present invention greatly increases carbon efficiency and reduces the generation of carbon dioxide.

Abstract: A method of producing 1,3-butadiene by the oxidative dehydrogenation of n-butene using a continuous-flow dual-bed reactor designed such that two kinds of catalysts charged in a fixed-bed reactor are not physically mixed. More particularly, a method of producing 1,3-butadiene by the oxidative dehydrogenation of n-butene using a C4 mixture including n-butene and n-butane as reactants and using a continuous-flow dual-bed reactor in which a multi-component bismuth molybdate catalyst and a zinc ferrite catalyst having different reaction activity in the oxidative dehydrogenation reaction of n-butene isomers (1-butene, trans-2-butene, cis-2-butene).

Abstract: Disclosed herein is a catalyst, including, in one example: a carrier, a polymer electrolyte multilayer film formed on the carrier, and metal particles dispersed in the polymer electrolyte multilayer film. The catalyst can be easily prepared, and can be used to produce hydrogen peroxide in high yield in the presence of a reaction solvent including no acid promoter.

Abstract: A fuse circuit includes a program unit, a sensing unit and a control unit. The program unit is programmed in response to a program signal, and outputs a program output signal in response to a sensing enable signal. The sensing unit includes a variable resistor unit that has a resistance that varies based on a control signal, and generates a sensing output signal based on the resistance of the variable resistor unit and the program output signal. The control unit generates the control signal having a value changed depending on operation modes, and performs a verification operation with respect to the program unit based on the sensing output signal to generate a verification result. The program unit may be re-programmed based on the verification result.

Abstract: The present invention relates to a preparation method for alcohol by reacting carboxylic acid, alcohol, and hydrogen using hydrogenation catalysts. More specifically, the invention relates to a method for preparing alcohol by performing esterification and hydrocracking in a one-step process using hydrogenation catalysts instead of a two-step process. According to the invention, alcohol is prepared from carboxylic acid through esterification and hydrogenation in a one-step process using hydrogenation catalysts. Therefore, production costs and by-product treatment costs can be reduced in comparison to a two-step process. In addition, the invention is effective and economical since it can produce alcohol at relatively high yield by a simple process. Further, the invention allows high yield at relatively lower pressure when compared to alcohol production from carboxylic acid through hydrogenation without esterification and solves the problems of leaching by catalysts.

Abstract: This invention relates to a petroleum refining method for producing high value-added clean petroleum products and aromatics (Benzene/Toluene/Xylene) together, by which low pollution petroleum products including liquefied petroleum gas or low-sulfur gas oil and aromatics can be efficiently produced together from a fluid catalytic cracked oil fraction.

Abstract: Disclosed herein is a catalyst for xylene isomerization, including: a carrier including a zeolite, having a molar ratio of silica to alumina of 20˜100, impregnated with or mixed with a metal salt (I) having an amount of a metal component of 0.05˜5.0 wt % relative to a zeolite, and an inorganic binder, in which an amount of the zeolite is 10˜90 wt % based on the total amount of the carrier, wherein the carrier is supported with a VIII group metal such that an amount of the VIII group metal is 0.001˜3.0 wt % based on a total amount of the catalyst, or is supported with the VII group metal additionally supported with tin, bismuth or lead such that an amount of the tin, bismuth or lead is 0.01-5.0 wt % based on the total amount of the catalyst, and a method of producing the catalyst.

Abstract: The present invention relates to a method of producing aromatic products (benzene/toluene/xylene) and olefin products from petroleum fractions obtained by fluid catalytic cracking, and, more particularly, to a method of producing products comprising high-concentration aromatic products and high value-added light olefin products from light cycle oil obtained by fluid catalytic cracking.

Abstract: This invention relates to a bismuth molybdate catalyst, a preparation method thereof, and a method of preparing 1,3-butadiene using the same, and to a bismuth molybdate catalyst, a preparation method thereof, and a method of preparing 1,3-butadiene using the same, in which 1,3-butadiene can be prepared through oxidative dehydrogenation directly using a C4 mixture including n-butene and n-butane as a reactant in the presence of a mixed-phase bismuth molybdate catalyst including ?-bismuth molybdate (Bi2Mo3On) and ?-bismuth molybdate (Bi2MoO6). According to this invention, the C4 raffinate, containing many impurities, is used as a reactant, without an additional n-butane separation process, thus obtaining 1,3-butadiene at high yield.

Abstract: A method of producing 1,3-butadiene by the oxidative dehydrogenation of n-butene using a continuous-flow dual-bed reactor designed such that two kinds of catalysts charged in a fixed-bed reactor are not physically mixed. More particularly, a method of producing 1,3-butadiene by the oxidative dehydrogenation of n-butene using a C4 mixture including n-butene and n-butane as reactants and using a continuous-flow dual-bed reactor in which a multi-component bismuth molybdate catalyst and a zinc ferrite catalyst having different reaction activity in the oxidative dehydrogenation reaction of n-butene isomers (1-butene, trans-2-butene, cis-2-butene).

Abstract: Disclosed herein is a method of regenerating a titanium-containing molecular sieve catalyst. Particularly, this invention provides a method of regenerating a titanium-containing molecular sieve catalyst used in epoxidation of olefin through simple treatment using a mixture solvent comprising aqueous hydrogen peroxide and alcohol. According to the method of this invention, when the catalyst having decreased activity is regenerated, the activity of the regenerated catalyst is equal to that of new catalyst and can be maintained stable for a long period of time.

Abstract: A method of producing a mixed manganese ferrite catalyst, and a method of preparing 1,3-butadiene using the mixed manganese ferrite catalyst. Specifically, a method of producing a mixed manganese ferrite catalyst through a coprecipitation method which is performed at a temperature of 10˜40° C., and a method of preparing 1,3-butadiene using the mixed manganese ferrite catalyst through an oxidative dehydrogenation reaction, in which a C4 mixture containing n-butene, n-butane and other impurities is directly used as reactants without performing additional n-butane separation process or n-butene extraction. 1,3-butadiene can be prepared directly using a C4 mixture including n-butane at a high concentration as a reactant through an oxidative hydrogenation reaction without performing an additional n-butane separation process, and 1,3-butadiene, having high activity, can be also obtained in high yield for a long period of time.

Abstract: A supporting device for a display unit for rotating a display screen to be oriented vertically. The supporting device includes a fixed member mounted on a base, an elevating member secured to the fixed member to be lifted or lowered, a pivot bracket rotatably coupled to an upper end of the elevating member while being secured to a rear surface of the display unit, an operating lever having an upper portion rotatably coupled to the upper end of the elevating member, a holder formed at the fixed member to allow the operating lever to be caught therein when being rotated rearward in a lifted state of the elevating member, a horizontally movable member secured to the upper end of the elevating member, and a cam portion formed at the pivot bracket.

Abstract: This invention relates to a method of preparing multicomponent bismuth molybdate catalysts composed of four metal components and a method of preparing 1,3-butadiene using the catalyst, and particularly, to multicomponent bismuth molybdate catalysts composed of a divalent cationic metal, a trivalent cationic metal, bismuth and molybdenum, a preparation method thereof, and a method of preparing 1,3-butadiene from a C4 mixture including n-butene and n-butane using oxidative dehydrogenation. According to this invention, it is possible to prepare catalysts having high activity for the preparation process of 1,3-butadiene only using four metal components as shown through systematic investigation of types and ratios of metal components, unlike conventional multicomponent metal oxide catalysts having a complicated composition of metal components.

Abstract: Disclosed is a process for preparing dimethyl ether, including a) reacting methanol containing 0-80 mol % of water in the presence of a dehydration catalyst, b) transferring the reaction product into a single separation column, thus separating dimethyl ether, water, and unreacted methanol, c) withdrawing dimethyl ether and withdrawing unreacted methanol from the sidestream of the single separation column, and d) recyling the unreacted methanol to the a) reacting the methanol. Dimethyl ether may be prepared from water-containing methanol, and the separation and withdrawal of dimethyl ether, water, and unreacted methanol may be realized using a single column, thus reducing the investment cost and the operating cost.

Abstract: A display apparatus having a casing in which an opening part is formed, includes: a liquid crystal display panel that is supported by the casing so that an image can be displayed through an opening part; a backlight unit that is provided behind the liquid crystal display panel and has a light source that emits light; a shield cover that is provided behind the backlight unit and is supported by at least one of the backlight unit and the casing; and a cooling fan unit that is combined to the shield cover and supplies cooling air to the backlight unit.

Abstract: A supporting device includes a support, serving to support a main body of the display unit, formed by injection molding using a transparent material. A display unit includes the supporting device. The display unit includes a main body having a screen and a supporting device to support the main body. The supporting device includes a support connected to the main body and a stand connected to the lower part of the support. The support includes a transparent member formed by injection molding using a transparent material. The transparent member is disposed between the main body and the stand to support the display unit, and is formed by insert injection molding.

Abstract: Disclosed is a method of recovering 1,3-butadiene from a C4 stream containing butane, isobutane, 2-butene, 1-butene, isobutene, butadiene and acetylene. The process of recovering highly pure 1,3-butadiene includes acetylene conversion for selectively converting acetylene through liquid-phase hydrogenation, so that the acetylene content is decreased to 70 wt ppm or less, and 1,3-butadiene extraction using an extractive distillation column, a pre-separator, a solvent stripping column, a solvent recovery column, and a purification column. Through the acetylene conversion, the concentration of vinylacetylene is decreased to 70 wt ppm or less, after which 1,3-butadiene is recovered using only one extractive distillation column, thereby considerably decreasing the degree of utility and the loss of streams in the course of extraction. The number of units necessary for the process is decreased, thus remarkably reducing the time during which impurities can accumulate in a processing unit.

Abstract: This invention relates to a method of preparing a multicomponent bismuth molybdate catalyst by changing the pH of a coprecipitation solution upon coprecipitation and a method of preparing 1,3-butadiene using the catalyst. The multicomponent bismuth molybdate catalyst, coprecipitated using a solution having an adjusted pH, the preparation method thereof, and the method of preparing 1,3-butadiene through oxidative dehydrogenation using a C4 mixture including n-butene and n-butane as a reactant are provided. The C4 raffinate, containing many impurities, is directly used as a reactant without an additional process for separating n-butane or extracting n-butene, thus obtaining 1,3-butadiene at high yield. The activity of the multicomponent bismuth molybdate catalyst can be simply increased through precise pH adjustment upon coprecipitation, which is not disclosed in the conventional techniques.