Abstract:
PURPOSE: A plate type steam reformer which effectively preheats reforming reactor as well as high and low temperature shift reactors and controls flow amount of flue gas using damper, thereby controlling temperature of each reactor to a desired temperature to obtain gas containing sufficient hydrogen is provided. CONSTITUTION: The plate type steam reformer is characterized in that a plate type burner(1) capable of heating a large area is installed at the lower side as a heat source, a high temperature shift reactor(4) requiring a relatively lower high temperature is stacked in the upper side of the reforming reactor(3) as a reforming reactor(3) requiring a relatively higher high temperature is being stacked in the upper side of the burner(1), a low temperature reforming reactor(5) requiring low temperature is stacked in the upper side of the high temperature shift reactor(4), and a relevant separation plate(7) is installed between each of the reactors(3,4,5) so that required heat is supplied to the reactors(3,4,5) as combustion flue gas of high temperature generated from the burner(1) is passing through the respective reactors(3,4,5) in such a way that the combustion flue gas of high temperature encircles the reactors(3,4,5).
Abstract:
PURPOSE: A catalyst capable of improving conversion ratio of dehydrogenation reaction of aromatic hydrocarbons such as ethyl benzene when using carbon dioxide as oxidizing agent is provided, and a dehydrogenation method of aromatic hydrocarbons using the catalyst is provided. CONSTITUTION: The iron oxide supported catalyst for dehydrogenation reaction of aromatic hydrocarbons is represented as the following general formula 1: (Fe¬IIxFe¬IIIyOz)/S, where iron oxide of the initial state satisfies the conditions that x=0.1 to 2, x+y=3, z=(2x+3y)/2, and S is a catalyst support selected from the group consisting of zeolite, activated carbon, γ-alumina, and silica, wherein the iron oxide is contained in the catalyst support in a concentration of 0.1 to 50 wt.%. The dehydrogenation method is characterized in that the aromatic hydrocarbons are dehydrogenated at a temperature of 500 to 700 deg.C by using carbon dioxide as diluting gas, wherein the aromatic hydrocarbons is ethyl benzene, and the diluting gas of carbon dioxide is used in the amount range of 1 to 100 times of aromatic hydrocarbons.
Abstract:
PURPOSE: Provided is a catalyst for dehydrogenation of alkylaromatic hydrocarbons, which has improved reaction activity and excellent selectivity to target products in the case that the catalyst is applied to dehydrogenation of alkylaromatic hydrocarbons conducted in the presence of moisture, by adding a specific amount of zirconium to conventional iron oxides in the form of cerium-zirconium complex oxides. CONSTITUTION: In a catalyst comprising iron oxide, potassium oxide, cerium oxide, calcium oxide, molybdenum oxide and magnesium oxide, the present invention is characterized in that the catalyst further contain zirconium oxide in an amount of 0.5 to 10 wt.% and cerium oxide in an amount of 0.5 to 8.0 wt.%, based on the total weight of the catalyst.
Abstract:
PURPOSE: Provided are the preparation method and the equipments of inorganic materials such as porous molecules, layered structure compounds and ceramic devices using continuous microwave synthesis which reduces the synthesis and crystallization time. Mass production is possible by the method because it is a continuous process and the use of organic template material is not needed when the porous molecular sieve are made. CONSTITUTION: The method includes the steps of preparing the precursor solution of the inorganic materials such as porous molecules with micropore, two-dimensional layered structure compounds and the ceramic materials; introducing the above solution into a tube type reactor continuously; and irradiating microwave with 60-1200 watt at the atmospheric pressure of 1 to 400 psi. The above porous molecules are selected from zeolite with pore size of 3-8Å, zeolite substituted by transition metals and mesoporous materials with a pore size of 20-150Å chosen from aluminosilicate, aluminophosphate and silicoaluminophosphate and 0-20wt.% of the above porous molecules with the size of 50-500 nm nuclear seed are included in the synthetic solution. The above two-dimensional layered structure compounds are selected from hydrotalcite type layered double hydrates and the mixed oxides derived from them. The above ceramic materials are chosen from metal ferrite compounds containing Zn, Ni, Mn and Co, spinel oxides. The equipment includes input tank of synthesis solution, tube type reactor, cylindrical reactor and the microwave reactor(30) equipped with microwave irradiation device(33).
Abstract:
PURPOSE: Provided are a selective hydrogenation catalyst and a selective hydrogenation process of diolefin compound using the catalyst. The above catalyst is tetragonal Ni/Zr type and is used in the selective hydrogenation of diolefin compounds that are contained in the carbohydrate mixtures into mono-olefin compounds. CONSTITUTION: The preparation method of the above catalyst comprises: 0.1-5wt.% (based on the hydrate) of Ni alone or having 0.1-5mol.% (based on Zr carrier) of a cocatalyst selected from Pd, Pt, Ag, Cu, Mo and B and its carrier of Zr alone or modified by one metal chosen from Ca, lanthanide metals such as Se and La, IIIB group metal(silicone) or IVB group metal(Al). The above selective hydrogenation is conducted in the temperature range of 80 to 250°C at a pressure of 1 to 12 atm. and at space velocity of 4 to 12/h (based on the volume of liquid reactant).
Abstract:
PURPOSE: According to steam reforming reaction using nickel reforming catalyst(Ni/Ce-ZrO2) where synthesis gas containing hydrogen as primary ingredient is prepared from natural gas comprising primary methane, the present nickel reforming catalyst(Ni/Ce-ZrO2) has superior methane conversion rate when used as catalyst for steam reforming. CONSTITUTION: The nickel reforming catalyst(Ni/Ce-ZrO2) for preparing synthesis gas is characterized in that zirconia coated with cerium 0.01-1.0mol.% is further supported with nickel 5-20wt.%. The method for preparing synthesis gas from natural gas by steam reforming is performed by steam reforming reaction under operation conditions that reaction a mole ratio of methane and steam is 1:2-7, a reaction temperature is 600 to 1000deg.C, a reaction pressure is 0.5-30atm and a space velocity is 1000-500000cc.
Abstract:
본 발명은 하이드록시화 방향족 화합물의 알킬화 방법에 관한 것으로서, 더욱 상세하게는 산성도와 동공의 크기가 적절히 선택/조절된 다공성 고체산 촉매상에서 올레핀이나 알콜을 이용하여 50 ∼ 200℃ 및 1 ∼ 20 기압의 조건하에서 하이드록시화 방향족 화합물의 알킬화를 수행하여 기존의 균일 촉매계에 의한 액상 알킬화 반응이 갖는 단점을 극복하고, 높은 선택도와 전환율로 하이드록시화 방향족 화합물을 알킬화하는 방법에 관한 것이다.
Abstract:
본 발명은 과량 산소 조건에서 배출되는 질소 산화물을 선택적으로 환원할 수 있는 귀금속 담지 제올라이트 촉매의 제조 방법에 관한 것으로서, 팔라듐(Pd), 백금(Pt), 로듐(Rh), 금(Au)을 포함하는 촉매 활성 귀금속 성분을 높은 실리카 함량(Si/Al〉10)의 제올라이트에 담지하는데 있어서 새로운 담지법을 이용하므로써, 천연가스를 환원제로 한 고활성 탈질 촉매를 쉽고 재현성 있게 제조할 수 있도록, 제올라이트 세공을 보호할 수 있는 유기물질을 미리 세공 내에 채워 넣은 상태에서 활성 귀금속 촉매성분을 담지하는 함침 또는 이온 교환법에 의하여, 고활성 탈질 촉매 설계에 필수적인 귀금속 성분을 제올라이트 세공의 원하는 위치에 정확히 담지할 수 있다. 이와 같은 새로운 방법에 의하여 제조된 촉매는, 제올라이트 세공을 보호하지 않은 상태에서 활성 귀금속 성분을 담지하는 종래의 함침법에 비하여 높은 탈질활성을 나타낼 뿐만 아니라 과량 산소 분위기 하에서도 천연가스를 환원제로 하여 높은 활성으로 질소 산화물을 선택적 환원할 수 있으므로, 가스터빈이나 보일러 등과 같은 고정원이나 린번 엔진과 같이 과량의 산소가 포함되어 있는 배출가스로부터의 질소 산화물 제거에 유용하다.
Abstract:
PURPOSE: A method for preparing a noble metal-dipped zeolite-based denitrifying catalyst is provided, which catalyst reduces selectively nitrogen compounds in the presence of excess oxygen by using natural gas as a reducing agent to remove the nitrogen gas. CONSTITUTION: A method comprises the steps of filling the cavity of zeolite with an organic compound of molecular weight 100-250; and dipping catalytically active noble metals into the zeolite. Preferably the noble metal is selected from the group consisting of platinum, palladium, rhodium and gold. The organic compound is alcohols or amines containing a secondary propyl group, a tertiary butyl group or a tertiary pentyl group; salts of OH, Cl, Br or I of amines containing a secondary propyl group, a tertiary butyl group or a tertiary pentyl group; or quinones. The amount of noble metals is 0.3-2.0 wt% based on the total weight of the dry catalyst, and the amount of the organic compound is 0.5-5 mol per 1 mol Al of zeolite. Preferably 0.5-5.0 wt% of titiana, vanadia or ceria is added further.