ε-카프로락탐의 제조 방법
    186.
    发明授权
    ε-카프로락탐의 제조 방법 有权
    生产β-碳青霉烯的方法

    公开(公告)号:KR101100054B1

    公开(公告)日:2011-12-29

    申请号:KR1020040051544

    申请日:2004-07-02

    CPC classification number: C07D201/04 Y02P20/52

    Abstract: ε-카프로락탐은 고체 촉매 입자를 옥심 포함 가스와 접촉시키기 위해 촉매 층을 유동화하면서 가스 분산판의 다수의 구멍 (평균 직경: 약 3 mm 이하) 을 통해 시클로헥사논 옥심 포함 가스를 고체 촉매 입자의 층에 도입하는 단계를 포함하는 방법으로 얻는다.
    상기의 제조 방법으로, 시클로헥사논 옥심 포함 원료 가스로부터 시클헥사논 옥심의 고전화율 및 ε-카프로락탐에 대한 고선택율로 ε-카프로락탐을 제조할 수 있다.
    ε-카프로락탐

    금속 이온이 담지된 세공성 촉매, 이의 제조방법 및 이를이용한 ε-카프로락탐의 제조방법
    187.
    发明公开
    금속 이온이 담지된 세공성 촉매, 이의 제조방법 및 이를이용한 ε-카프로락탐의 제조방법 失效
    金属离子注入多孔催化剂,其制备方法和使用该方法制备ε-吡咯烷酮的方法

    公开(公告)号:KR1020040042720A

    公开(公告)日:2004-05-20

    申请号:KR1020020071308

    申请日:2002-11-15

    CPC classification number: B01J21/08 B01J35/1019 B01J37/08 B01J37/30 C07D201/04

    Abstract: PURPOSE: Provided are a metal ion impregnated porous catalyst and a method for preparing thereof, which is able to increase the yield of a conversion rate of cyclohexanone oxime and ε-caprolactam and provides safe, economical, environmental-friendly and life span extended metal ion, and a method for preparing ε-caprolactam from cyclohexanone oxime using the catalyst. CONSTITUTION: The metal ion impregnated porous catalyst has pores formed by metal oxide pillar introduced between layers of layered silica compound, wherein the metal ion is impregnated in pores. The method comprises steps of (a) synthesizing a layered silica compound; (b) acid-ion exchanging the synthesized layered silica compound by acid titration; (c) forming pores between layers of layered silica compound by adding organic metal to the acid-ion exchanged layered silica compound and sintering; and (d) supporting the surface of the pores in metal ion by adding an aqueous solution of the metal ion thereto and sintering. The ε-caprolactam is prepared by gaseous beckmann conversion of cyclohexanone oxime solution using the metal ion impregnated porous catalyst.

    Abstract translation: 目的:提供一种金属离子浸渍多孔催化剂及其制备方法,其能够提高环己酮肟和ε-己内酰胺的转化率的产率,并提供安全,经济,环保和寿命延长的金属离子 以及使用该催化剂从环己酮肟制备ε-己内酰胺的方法。 构成:金属离子浸渍多孔催化剂具有由层状二氧化硅化合物层之间引入的金属氧化物柱形成的孔,其中金属离子浸渍在孔中。 该方法包括以下步骤:(a)合成层状二氧化硅化合物; (b)通过酸滴定将合成的层状二氧化硅化合物进行酸离子交换; (c)通过向酸离子交换的层状二氧化硅化合物中加入有机金属并烧结而在层状二氧化硅化合物的层之间形成孔; 和(d)通过向其中加入金属离子的水溶液并进行烧结来支撑金属离子中的孔的表面。 使用金属离子浸渍的多孔催化剂,通过环己酮肟溶液的气态贝克曼转化制备ε-己内酰胺。

    펜타실-형 결정성 제올라이트의 제조 방법 및 그것을사용하는 ε-카프로락탐의 제조 방법
    189.
    发明公开
    펜타실-형 결정성 제올라이트의 제조 방법 및 그것을사용하는 ε-카프로락탐의 제조 방법 有权
    生产PENTASIL型晶体沸石和ε-CAPROLACTAM的生产

    公开(公告)号:KR1020010066865A

    公开(公告)日:2001-07-11

    申请号:KR1020000034494

    申请日:2000-06-22

    Abstract: PURPOSE: A method for producing a pentasil type crystalline zeolite having excellent catalytic activity and reproductivity is provided. CONSTITUTION: This method for producing a pentasil type crystalline zeolite comprises (i) compounding a silicon compound with water and tetra-n-propylammonium hydroxide; (ii) obtaining a reaction solution containing a zeolite crystal by hydrothermal reaction from a mixed solution obtained by the 1st step; (iii) separating the reaction solution obtained by the 2nd step into the zeolite crystal and a solution; (iv) baking the zeolite crystal obtained by the 3rd step; and (v) treating the zeolite crystal baked by the 4th step with an aqueous solution containing ammonia and/or ammonium salt and has the molar ratio of hydroxide to silicon of 0.1-0.4 and the molar ratio potassium ion to silicon of 0-0.1 in the mixed solution prepared in the 1st step. This method for producing ε-caprolactam comprises using the pentasil type crystalline zeolite as a catalyst obtained by the method and subjecting cyclohexanone. oxime to Beckmanns rearrangernent reaction under a vapor-phase condition.

    Abstract translation: 目的:提供催化活性和再生性优异的pentasil型结晶沸石的制造方法。 构成:用于制备pentasil型结晶沸石的方法包括(i)将硅化合物与水和四正丙基氢氧化铵混合; (ii)从通过第一步骤得到的混合溶液通过水热反应获得含有沸石晶体的反应溶液; (iii)将由第二步获得的反应溶液分离成沸石晶体和溶液; (iv)焙烧通过第3步获得的沸石晶体; 和(v)用含有氨和/或铵盐的水溶液处理由第四步骤焙烧的沸石晶体,并且氢氧化物与硅的摩尔比为0.1-0.4,钾离子与硅的摩尔比为0-0.1 在第一步中制备的混合溶液。 该ε-己内酰胺的制造方法包括使用pentasil型结晶沸石作为通过该方法获得的催化剂并对环己酮进行处理。 肟到贝克曼在气相条件下反向反应。

    메탄술폰산의 존재 하에 시클로도데칸의 광니트로화 및 벡크만 재배열에 의한 라우릴락탐의 제조 방법
    190.
    发明公开
    메탄술폰산의 존재 하에 시클로도데칸의 광니트로화 및 벡크만 재배열에 의한 라우릴락탐의 제조 방법 失效
    在甲磺酸存在下环孢菌素和贝克曼替代光合作用生产劳伦沙星的方法

    公开(公告)号:KR1020000023183A

    公开(公告)日:2000-04-25

    申请号:KR1019990039567

    申请日:1999-09-15

    CPC classification number: C07D201/04

    Abstract: PURPOSE: A process for production of lauryllactam which is useful as a monomer for producing a polyamide 12 type polymer is provided by which defects caused by using sulfonic acid in a conventional process can be reduced by using methane sulfonic acid. CONSTITUTION: A process for production of lauryllactam comprises the steps of: reacting acyclododecane, a nitrating agent and a hydrogen chloride which are dissolved in an organic solvent such as a chloroform or a chlorobenzene in the presence of a methane sulfonic acid to give a cyclododecanone oxime; and subjecting the oxime to Beckmann rearrangement in the presence of the methane sulfonic acid to give the objective lauryllactam.

    Abstract translation: 目的:提供用作生产聚酰胺12型聚合物的单体的十二烷基内酰胺的制造方法,通过使用甲磺酸可以降低常规方法中使用磺酸引起的缺陷。 构成:生产月桂基内酰胺的方法包括以下步骤:在甲磺酸存在下,将溶于有机溶剂如氯仿或氯苯的acyclododecane,硝化剂和氯化氢反应,得到环十二烷酮肟 ; 并在甲磺酸存在下使肟进行贝克曼重排,得到目的月桂基内酰胺。

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