Abstract: The present invention relates to a ferrite-based catalyst composite, a method of preparing the same, and a method of preparing butadiene using the same. More particularly, the present invention provides a ferrite-based catalyst composite having a shape that allows effective dispersion of excess heat generated in a butadiene production process and prevention of catalyst damage and side reaction occurrence by reducing direct exposure of a catalyst to heat, a method of preparing the ferrite-based catalyst composite, and a method of preparing butadiene capable of lowering the temperature of a hot spot and reducing generation of Cox by allowing active sites of a catalyst to have a broad temperature gradient (profile) during oxidative dehydrogenation using the ferrite-based catalyst composite, and thus, providing improved process efficiency.

Abstract: The present invention relates to a catalyst for oxidative dehydrogenation and a method of preparing the same. More particularly, the present invention provides a catalyst for oxidative dehydrogenation allowing oxidative dehydrogenation reactivity to be secured while increasing a first pass yield, and a method of preparing the catalyst.

Abstract: Provided is a catalyst for oxidative dehydrogenation, a method of preparing the catalyst, and a method of performing oxidative dehydrogenation using the catalyst. The catalyst for oxidative dehydrogenation has improved durability and fillability by including a porous support coated with a metal oxide (AB2O4) according to Equation 1 of the present invention, wherein the metal oxide exhibits activity during oxidative dehydrogenation. Therefore, when the catalyst is used in oxidative dehydrogenation of butene, the conversion rate of butene and the selectivity and yield of butadiene may be greatly improved.

Abstract: The present disclosure relates to a method of preparing a zinc ferrite catalyst. More particularly, the present invention relates to a method of preparing a zinc ferrite catalyst comprising a) a step of dissolving a zinc precursor and an iron (III) precursor in water to prepare an aqueous metal precursor solution; b) a step of precipitating a solid catalyst precursor while vaporizing water in the aqueous metal precursor solution; and c) a step of firing the precipitated solid catalyst precursor to prepare a zinc ferrite catalyst. In accordance with the present disclosure, the method of preparing a zinc ferrite catalyst can be simply carried out without a pH adjustment step and can secure reproducibility.

Abstract: The present invention relates to a catalyst for coating a surface of a porous material and a method of treating the surface of the porous material. More particularly, when the catalyst for coating a surface of a porous material and the method of treating the surface of the porous material of the present invention are used for butadiene synthesis reaction under high gas space velocity and high pressure conditions, heat generation may be easily controlled and differential pressure may be effectively alleviated, thereby providing improved reactant conversion rate and product selectivity.

Abstract: The present invention relates to a catalyst for oxidative dehydrogenation and a method of preparing the same. More particularly, the present invention provides a catalyst for oxidative dehydrogenation allowing oxidative dehydrogenation reactivity to be secured while increasing a first pass yield, and a method of preparing the catalyst.

Abstract: Provided are a method of preparing a multicomponent bismuth-molybdenum composite metal oxide catalyst, and a multicomponent bismuth-molybdenum composite metal oxide catalyst prepared thereby. According to the preparation method, since the almost same structure as that of a typical quaternary bismuth-molybdenum catalyst may be obtained by performing two-step co-precipitation, i.e., primary and secondary co-precipitation, of metal components constituting the catalyst, the reduction of catalytic activity due to the deformation of the structure of the catalyst may be suppressed.

Abstract: A method of preparing butadiene that includes supplying butene, oxygen, nitrogen, and steam into a reactor filled with a metal oxide catalyst, and performing an oxidative dehydrogenation reaction at a temperature of 300 to 450° C. as a reaction step; after the reaction step, maintaining supplying the butene, oxygen, nitrogen, and steam within a range within which the flow rate change of the butene, oxygen, nitrogen, and steam is less than ±40%, or stopping supplying the butene, and cooling the reactor to a temperature range of 200° C. or lower and higher than 70° C. as a first cooling step; and after the first cooling step, stopping supplying the butene, oxygen, nitrogen, and steam or stopping at least supplying the butene, and cooling the reactor to a temperature of 70° C. or lower as a second cooling step.

Abstract: A ferrite catalyst for oxidative dehydrogenation and a method of preparing the same. The ferrite catalyst is prepared using an epoxide-based sol-gel method, wherein a step of burning includes a first burning step, in which burning is performed at a temperature of 70 to 200° C.; and a second burning step, in which burning is performed after the temperature is raised from a temperature in the range of greater than 200° C. to 250° C. to a temperature in the range of 600 to 900° C.

Abstract: Disclosed are a catalyst for oxidative dehydrogenation and a method of preparing the same. More particularly, a catalyst for oxidative dehydrogenation of butene having a high butene conversion rate and superior side reaction inhibition effect and thus having high reactivity and high selectivity for a product by preparing metal oxide nanoparticles and then fixing the prepared metal oxide nanoparticles to a support, and a method of preparing the same are provided.

Abstract: The present disclosure relates to a method of preparing a zinc ferrite catalyst. More particularly, the present invention relates to a method of preparing a zinc ferrite catalyst comprising a) a step of dissolving a zinc precursor and an iron (III) precursor in water to prepare an aqueous metal precursor solution; b) a step of precipitating a solid catalyst precursor while vaporizing water in the aqueous metal precursor solution; and c) a step of firing the precipitated solid catalyst precursor to prepare a zinc ferrite catalyst. In accordance with the present disclosure, the method of preparing a zinc ferrite catalyst can be simply carried out without a pH adjustment step and can secure reproducibility.

Abstract: The present invention relates to a ferrite-based catalyst composite, a method of preparing the same, and a method of preparing butadiene using the same. More particularly, the present invention provides a ferrite-based catalyst composite having a shape that allows effective dispersion of excess heat generated in a butadiene production process and prevention of catalyst damage and side reaction occurrence by reducing direct exposure of a catalyst to heat, a method of preparing the ferrite-based catalyst composite, and a method of preparing butadiene capable of lowering the temperature of a hot spot and reducing generation of Cox by allowing active sites of a catalyst to have a broad temperature gradient (profile) during oxidative dehydrogenation using the ferrite-based catalyst composite, and thus, providing improved process efficiency.

Abstract: The present invention relates to a catalyst for coating a surface of a porous material and a method of treating the surface of the porous material. More particularly, when the catalyst for coating a surface of a porous material and the method of treating the surface of the porous material of the present invention are used for butadiene synthesis reaction under high gas space velocity and high pressure conditions, heat generation may be easily controlled and differential pressure may be effectively alleviated, thereby providing improved reactant conversion rate and product selectivity.

Abstract: The present invention relates to a method of preparing a catalyst for oxidative dehydrogenation. More particularly, the method of preparing a catalyst for oxidative dehydrogenation includes a first step of preparing an aqueous iron-metal precursor solution by dissolving a trivalent cation iron (Fe) precursor and a divalent cation metal (A) precursor in distilled water; a second step of obtaining a slurry of an iron-metal oxide by reacting the aqueous iron-metal precursor solution with ammonia water in a coprecipitation bath to form an iron-metal oxide (step b) and then filtering the iron-metal oxide; and a third step of heating the iron-metal oxide slurry. In accordance with the present invention, a metal oxide catalyst, as a catalyst for oxidative dehydrogenation, having a high spinel phase structure proportion may be economically prepared by a simple process.

Abstract: Disclosed are a method of preparing conjugated diene and a device therefor. More particularly, disclosed a method of preparing conjugated diene, wherein generated gas including butadiene is cooled and then water discharged at a lower part is not directly treated as waste water and subjected to byproduct removal and steam-extraction to utilize converted steam, and an installation issue of an existing biological waste water disposal equipment due to an excessive amount of byproducts can be resolved, and a device therefor are disclosed.

Abstract: The present invention relates to a bismuth molybdate-based composite oxide catalyst having a microporous zeolite coating layer on the surface thereof and thus having high selectivity for 1,3-butadiene, a method of preparing the same, and a method of preparing 1,3-butadiene using the same. The catalyst has a microporous zeolite coating layer, and thus enables only gaseous products (light) to selectively pass through the zeolite coating layer, improving selectivity for 1,3-butadiene.

Abstract: Disclosed are a composite oxide catalyst for preparing butadiene and a method of preparing the same. More particularly, a composite oxide catalyst, for preparing butadiene, including a metal composite oxide and AlPO4, and a method of preparing the same are disclosed. According to the present disclosure, a composite oxide catalyst for preparing butadiene, which includes a specific binder material, prevents generation of ingredients with a high boiling point, has superior catalyst strength, catalytic activity and butadiene yield, and a method of preparing the same are provided.

Abstract: The present invention relates to a method of preparing butadiene. More particularly, the present invention relates to a method of preparing butadiene by feeding butene and oxygen into a reactor containing a composite metal oxide catalyst and performing oxidative dehydrogenation, wherein a mole ratio of the oxygen to the butene is 1.8 to 2.2. In accordance with the present invention, a method of preparing butadiene to secure long-term operation stability by maintaining the intensity of a catalyst despite oxidative dehydrogenation and not to decrease selectivity due to less side reaction is provided.

Abstract: Disclosed are a composite oxide catalyst for preparing butadiene and a method of preparing the same. More particularly, a composite oxide catalyst, for preparing butadiene, including a metal composite oxide and AlPO4, and a method of preparing the same are disclosed. According to the present disclosure, a composite oxide catalyst for preparing butadiene, which includes a specific binder material, prevents generation of ingredients with a high boiling point, has superior catalyst strength, catalytic activity and butadiene yield, and a method of preparing the same are provided.

Abstract: Disclosed are a catalyst composition for oxidative dehydrogenation and a method of preparing the same. More particularly, disclosed is a catalyst composition comprising a multi-ingredient-based metal oxide catalyst and a mixed metal hydroxide. The catalyst composition and the method of preparing the same according to the present disclosure may prevent loss occurring in a filling process due to superior mechanical durability and wear according to long-term use, may inhibit polymer formation and carbon deposition during reaction, and may provide a superior conversion rate and superior selectivity.