구리 성분 함유 산폐액을 사용한, 수소화 및 탈수소화반응용 구리/실리카 촉매의 제조 방법
    121.
    发明授权
    구리 성분 함유 산폐액을 사용한, 수소화 및 탈수소화반응용 구리/실리카 촉매의 제조 방법 失效
    구리성분함유산폐액을사Created,수소화및탈수소화반응용구리/실리카촉매의제조방

    公开(公告)号:KR100455665B1

    公开(公告)日:2004-11-06

    申请号:KR1020020015828

    申请日:2002-03-23

    Abstract: PURPOSE: A method for preparing copper/silica catalyst used in hydrogenation and dehydrogenation of organic compounds using acidic waste solution containing copper is provided. CONSTITUTION: The method for preparing copper/silica catalyst comprises a step (a) of preparing an aqueous copper solution by adding copper compound and arbitrary zinc compound to an acidic waste solution containing copper; a step (b) of preparing a copper slurry solution by adding a precipitant solution to the aqueous copper solution; a step (c) of preparing copper/silica slurry solution by adding colloidal silica solution to the copper slurry solution and stirring the colloidal silica solution and copper slurry solution; a step (d) of separating sediment and rinsing the separated sediment after aging the copper/silica slurry solution at a temperature of 50 to 100 deg.C; and a step (e) of drying and firing the rinsed sediment, wherein the precipitant is ammonia, or bicarbonate, carbonate or hydroxide of alkali metal, wherein the colloidal silica solution is added to the copper slurry solution in such a way that a weight ratio (CuO/SiO2) of copper oxide to silica in produced catalyst is in the range of 0.3-9.0/1, wherein zinc compound is used, and the colloidal silica solution is added to the copper slurry solution in such a way that a weight ratio (CuO/ZnO/SiO2) of copper oxide to zinc oxide to silica in produced catalyst is in the range of 0.3-9.0/0.01-3.0/1, wherein colloidal silica is stabilized by ammonium (NH4¬+) or Na¬+ or other alkali metal and has particle size of 4 to 60 nm, surface area of 100 to 300 m¬2/g and concentration of 5 to 60 wt.% based on silica, and wherein the aging is performed at a temperature of 50 to 100 deg.C for 0.5 to 24 hours.

    Abstract translation: 目的:提供一种使用含铜的酸性废溶液来制备用于有机化合物的氢化和脱氢的铜/二氧化硅催化剂的方法。 构成:铜/二氧化硅催化剂的制备方法包括:在含有铜的酸性废液中添加铜化合物和任意的锌化合物,制备铜水溶液的工序(a) 通过向所述铜水溶液中添加沉淀剂溶液来制备铜浆液的步骤(b); 通过向所述铜浆液中添加胶态二氧化硅溶液并搅拌所述胶态二氧化硅溶液和铜浆液来制备铜/二氧化硅浆料溶液的步骤(c); 步骤(d):在50-100℃的温度下老化铜/二氧化硅浆料溶液后分离沉淀物并冲洗分离的沉淀物; (e)干燥并烧制漂洗过的沉淀物,其中沉淀剂是氨或碳酸氢盐,碱金属的碳酸盐或氢氧化物,其中将胶体二氧化硅溶液以这样的方式加入到铜浆液中,使得重量比 在生产的催化剂中氧化铜与二氧化硅的比例(CuO / SiO2)为0.3-9.0 / 1,其中使用锌化合物,并将胶体二氧化硅溶液加入铜浆液中,使得重量比 在生产的催化剂中氧化铜与氧化锌形成二氧化硅的氧化物(CuO / ZnO / SiO2)在0.3-9.0 / 0.01-3.0 / 1范围内,其中胶体二氧化硅通过铵(NH 4 +)或Na + 其它碱金属,并且具有4至60nm的粒度,100至300μm2 / g的表面积和基于二氧化硅的5至60重量%的浓度,并且其中老化在50至100℃的温度下进行 持续0.5至24小时。

    결정성 금속수산화물과 수용성 금속화합물의 혼합물로부터 층상 혼합금속 수산화물을 제조하는 방법
    122.
    发明授权
    결정성 금속수산화물과 수용성 금속화합물의 혼합물로부터 층상 혼합금속 수산화물을 제조하는 방법 有权
    由结晶金属氢氧化物和水溶性金属化合物的混合物制备层状混合金属氢氧化物的方法

    公开(公告)号:KR100388097B1

    公开(公告)日:2003-06-18

    申请号:KR1020000029957

    申请日:2000-06-01

    Abstract: 고분자 물질 등에 첨가하기 위하여 적절한 입자크기를 갖고 얇은 판상을 이루며 표면적이 상대적으로 큰 범위에서 미세 특성제어가 용이한 결정성 층상 혼합금속 수산화물을 빠른 속도로 제조하는 방법이 개시되어 있다. 본 발명에 따르면, 결정성 M
    (II) (OH)
    2 (M
    (II) 는 +2 산화상태를 갖는 금속원소)와 결정성 M
    (III) (OH)
    3 (M
    (III) 는 +3 산화상태를 갖는 금속원소) 화합물의 물 분산물에, 이들 M
    (II) 및
    M
    (III) 금속원소를 포함하는 수용성 화합물류와 층간 음이온 성분을 포함하는 화합물을 첨가하고, 혼합물 용액의 pH를 조절하여 수용성 금속 성분을 점성을 띠는 젤 형태의 혼합금속 수산화물로 변환시키고, 상기 결정성 M
    (II) (OH)
    2 , M
    (III) (OH)
    3 와 수용성 금속 성분으로 부터 변형된 점성을 띠는 젤 형태의 금속수산화물을 포함하는 반응 혼합물로부터, 수열 반응과정을 거쳐, 결정성 층상 혼합금속 수산화물을 제조한다. 반응에 첨가되는 수용성 화합물류의 종류, 금속수산화물에 대한 수용성 금속화합물의 첨가 비율 및 방법, 층간 음이온 성분의 종류, 반응온도, 반응시간의 적절한 선택으로 생성물인 층상 혼합금속 수산화물의 입자크기를 0.2∼2μ범위, 입자형상을 규칙적인 육각 판상으로부터 불규칙적인 모양의 판상, 비표면적의 크기를 20∼90m
    2 /g 범위, 두께대 직경비를 10∼50 범위에서 유연하게 제어한다.

    에틸렌 삼량화 반응에서 1-헥센의 선택도를 증가시키는촉매계
    123.
    发明公开
    에틸렌 삼량화 반응에서 1-헥센의 선택도를 증가시키는촉매계 有权
    用于增加乙烯三聚物中1-HEXENE选择性的催化体系

    公开(公告)号:KR1020030029253A

    公开(公告)日:2003-04-14

    申请号:KR1020010061520

    申请日:2001-10-05

    CPC classification number: B01J31/18 B01J31/1805 B01J2531/62 C07C2/02

    Abstract: PURPOSE: Provided is a catalytic system that consists of Cr compound, ligand, alkylaluminium and halogen compound and for increasing 1-hexene selectivity in ethylene trimerization. CONSTITUTION: The catalytic system consists of chrome compound, ligand, alkylaluminium and halogen compound, wherein the ligand is a complex ligand being comprised of 1-coordinate ligand and 2-coordinate ligand, and wherein the 2-coordinate ligand includes at least two elements selected from oxygen (O), nitrogen (N) and sulfur (S), and the 1-coordinate ligand includes one element selected from oxygen (O), nitrogen (N), phosphorous (P), and sulfur (S), and further wherein the 2-coordinate ligand and the 1-coordinate ligand are included in the catalytic system with a mole ratio to chrome 0.5-1.5:1.

    Abstract translation: 目的:提供由Cr化合物,配体,烷基铝和卤素化合物组成的催化体系,并且用于在乙烯三聚中增加1-己烯选择性。 构成:催化体系由铬化合物,配位体,烷基铝和卤素化合物组成,其中配体是由1-配位配位体和2-配位配体构成的复合配体,其中2-配位配体包括至少两个选自 来自氧(O),氮(N)和硫(S),并且1-配位配体包括选自氧(O),氮(N),磷(P)和硫(S)中的一种元素, 其中2-配位配体和1-配位配位体以摩尔比为0.5-1.5:1包含在催化体系中。

    입자형상 및 크기제어가 가능한 멜라민시아누레이트복합체의 제조방법
    124.
    发明授权

    公开(公告)号:KR100369707B1

    公开(公告)日:2003-02-05

    申请号:KR1020010001196

    申请日:2001-01-09

    Abstract: PURPOSE: A method for preparing a crystalline melamine cyanurate composite is provided, to control the shape and size of particles by controlling the content of water-insoluble metal oxides and water-soluble hydroxides and the reaction conditions. CONSTITUTION: The method comprises the step of reacting melamine and cyanuric acid with a water-insoluble metal hydroxide or metal oxide and a water-soluble hydroxide. Preferably the reaction is carried out at a temperature of 80-100 deg.C for 0.5-2 hours. The water-insoluble metal hydroxide is selected from the group consisting of Mg(OH)2, Al(OH)3, Ca(OH)2 and magnesium/aluminum composite hydroxide; the water-insoluble metal oxide is selected from the group consisting of MgO, Al2O3, CaO and magnesium/aluminum composite oxide; and the water-soluble hydroxide is selected from the group consisting of NH4OH, LiOH, NaOH and KOH. Preferably the particle size of the water-insoluble metal hydroxide or metal oxide is 0.5-10 micrometers. The content of the water-insoluble metal hydroxide or metal oxide is 0.1-5.0 wt% based on the weight of solid reactant; and the content of water-soluble hydroxide is less than 20 wt% based on the weight of the water-insoluble metal hydroxide or metal oxide.

    Abstract translation: 目的:提供一种制备结晶三聚氰胺氰尿酸酯复合物的方法,通过控制水不溶性金属氧化物和水溶性氢氧化物的含量以及反应条件来控制颗粒的形状和尺寸。 组成:该方法包括使三聚氰胺和氰尿酸与水不溶性金属氢氧化物或金属氧化物和水溶性氢氧化物反应的步骤。 优选反应在80-100℃的温度下进行0.5-2小时。 水不溶性金属氢氧化物选自Mg(OH)2,Al(OH)3,Ca(OH)2和镁/铝复合氢氧化物; 水不溶性金属氧化物选自MgO,Al 2 O 3,CaO和镁/铝复合氧化物; 并且水溶性氢氧化物选自由NH 4 OH,LiOH,NaOH和KOH组成的组。 优选水不溶性金属氢氧化物或金属氧化物的粒度为0.5-10微米。 基于固体反应物的重量,水不溶性金属氢氧化物或金属氧化物的含量为0.1-5.0重量% 并且基于水不溶性金属氢氧化物或金属氧化物的重量,水溶性氢氧化物的含量小于20重量%。

    다원금속 복합산화물 촉매 및 이를 사용한 아크릴산의 제조방법
    125.
    发明授权
    다원금속 복합산화물 촉매 및 이를 사용한 아크릴산의 제조방법 失效
    多层复合氧化物催化剂及其制备丙烯酸的方法

    公开(公告)号:KR100264966B1

    公开(公告)日:2000-09-01

    申请号:KR1019980005952

    申请日:1998-02-25

    Abstract: PURPOSE: Disclosed are a complex metal oxide catalyst composed multiple metal elements and a preparing method of acrylic acid using the same. The catalyst has a composition form, Moa Vb Wc Pbd Cue Xf Yg (MhPMo12-i)jOk and the reaction for preparing acrylic acid is carried out under the reaction condition of low feed ratio of oxygen to acrolein and without a strong basic compound. CONSTITUTION: The complex metal oxide catalyst for preparing acrylic acid has a composition form, Moa Vb Wc Pbd Cue Xf Yg (MhPMo12-i)jOk, where X is one species of La, Ce, Sm, or Tl, Y is one species of Te, Sb, or Nb, M is Ce or Ru, and a, b, c, d, e, f, and g are atomic ratio values of respective elements. When a is 12, b, c, d, e, f, g, h, i, or j are 3-7, 1-6, 0.05-2, 0.5-4, 0.01-1, 0.01-1, 0-2, 0-3, and 0.01-0.2, respectively. And, silica, α-alumina, silicon carbide, or zirconium oxide may be used as a catalytic support. The preparation reaction of acrylic acid is carried out under the condition of temperature of 180-380deg.C, space velocity of 500-7000 h-1, feeding ratio of oxygen to acrolein of 0.5-2. Before the reaction, the catalyst is pre-treated at 200-450deg.C for 0.5-10 h in the mixed gas of acrolein, hydrocarbon such as propylene or methanol, and hydrogen.

    Abstract translation: 目的:公开了一种复合金属氧化物催化剂和多种金属元素的制备方法和丙烯酸的制备方法。 催化剂具有组成形式,Moa Vb Wc Pbd Cue Xf Yg(MhPMo12-i)jOk和制备丙烯酸的反应在氧气与丙烯醛的低进料比和没有强碱性化合物的反应条件下进行。 构成:用于制备丙烯酸的复合金属氧化物催化剂具有组成形式,Moa Vb Wc Pbd Cue Xf Yg(MhPMo12-i)jOk,其中X是La,Ce,Sm或Tl的一种,Y是一种 Te,Sb或Nb,M是Ce或Ru,a,b,c,d,e,f和g是各元素的原子比值。 当a为12时,b,c,d,e,f,g,h,i或j为3-7,1-6,0.05-2,0.5-4,0.01-1,0.01-1,0- 2,0-3和0.01-0.2。 并且,可以使用二氧化硅,α-氧化铝,碳化硅或氧化锆作为催化剂载体。 丙烯酸的制备反应在180-380℃,空速500-7000h-1,氧气与丙烯醛的进料比为0.5-2的条件下进行。 在反应之前,将催化剂在丙烯醛,烃类如丙烯或甲醇和氢气的混合气体中,在200-450℃预处理0.5-10小时。

    사이클로헥실아세테이트의 제조방법
    126.
    发明授权
    사이클로헥실아세테이트의 제조방법 失效
    制备环丙基乙酸酯的方法

    公开(公告)号:KR100165620B1

    公开(公告)日:1999-03-20

    申请号:KR1019950009575

    申请日:1995-04-24

    Abstract: 본 발명은 사이클로헥센과 아세트산을 반응시켜 사이클로헥실아세테이트를 제조하는 방법에 있어서, 하기 일반식(1)의 헤테로폴리산 금속이온 염을 고체산 촉매로 사용하여 사이클로헥실아세테이프의 생산성을 향상시키는 방법에 관한 것으로, 상기 산촉매는 대상 반응계에서 활성이 장기간 유지되며, 반응물에 대한 용해도가 낮고, 활성이 감소하였을 때 쉽게 재생시킬 수 있다.
    A
    x H
    nx SM
    12 O
    40 bH
    2 O (I)
    상기 식에서, A는 K 또는 C
    s 이고,
    x 는 0.1 내지 3 또는 4이고, n은 3 또는 4이고, S는 P 또는 Si 이고, M은 Mo 또는 W, 또는 이들의 조합이며, b는 0 내지 20이다.

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