RECOVERY OF CAPROLACTAM FROM NYLON-6 SCRAP
    131.
    发明申请
    RECOVERY OF CAPROLACTAM FROM NYLON-6 SCRAP 审中-公开
    从尼龙6刮刀回收卡波米特

    公开(公告)号:WO1997006137A1

    公开(公告)日:1997-02-20

    申请号:PCT/US1996012705

    申请日:1996-08-05

    CPC classification number: C07D201/12

    Abstract: A process for recovering monomer from multi-component waste material that includes a hydrolyzable polymer, includes contacting the multi-component waste material with water and subjecting the resulting mixture to heat and pressure to form a liquid aqueous portion and a water insoluble portion. The liquid aqueous portion mainly includes depolymerization products of the hydrolyzable polymer, and the water insoluble portion mainly includes components other than the depolymerization products. This mixture is cooled and the liquid aqueous portion and the water insoluble portion are separated. Monomer that formed the hydrolyzable polymer is recovered from the liquid aqueous solution.

    Abstract translation: 一种从包含可水解聚合物的多组分废料中回收单体的方法,包括使多组分废料与水接触并对所得混合物进行加热和压力以形成液体水性部分和不溶于水的部分。 液体水性部分主要包括可水解聚合物的解聚产物,水不溶部分主要包括解聚产物以外的成分。 将该混合物冷却,分离液体水性部分和水不溶性部分。 形成可水解聚合物的单体从液体水溶液中回收。

    PROCESS FOR THE RECOVERY OF CAPROLACTAM FROM WASTE CONTAINING NYLON BY EXTRACTION WITH ALKYL PHENOLS
    132.
    发明申请
    PROCESS FOR THE RECOVERY OF CAPROLACTAM FROM WASTE CONTAINING NYLON BY EXTRACTION WITH ALKYL PHENOLS 审中-公开
    通过用烷基酚提取含有尼龙的废物来回收卡波铵的方法

    公开(公告)号:WO1997003048A1

    公开(公告)日:1997-01-30

    申请号:PCT/NL1996000283

    申请日:1996-07-11

    Inventor: DSM N.V.

    CPC classification number: C07D201/12

    Abstract: A process for depolymerizing nylon (6) and recovering caprolactam from the depolymerized products by extraction with alkyl phenolic compounds. Process steps include (a) treating a first mixture comprising nylon (6) with water at a temperature between about 200 DEG C and about 400 DEG C to yield a second mixture comprising depolymerized nylon (6) components, wherein the second mixture contains caprolactam at a concentration between about 5 wt.% and about 35 wt.%; (b) optionally, separating insoluble material from the second mixture; (c) extracting the second mixture with an extraction agent to yield an aqueous raffinate third mixture and an organic phase fourth mixture comprising caprolactam and the extraction agent, wherein the extraction agent is an alkyl phenol having a boiling point higher than that of the caprolactam; (d) recovering caprolactam from the organic phase fourth mixture by distillation; (e) recycling the aqueous raffinate third mixture to step (a).

    Abstract translation: 通过用烷基酚类化合物提取,解聚尼龙(6)和从解聚产物中回收己内酰胺的方法。 工艺步骤包括(a)在约200℃至约400℃之间的温度下处理包含尼龙(6)的第一混合物与水,以产生包含解聚尼龙(6)组分的第二混合物,其中第二混合物含有己内酰胺 约5重量%至约35重量%的浓度; (b)任选地,从第二混合物中分离不溶物质; (c)用萃取剂萃取第二混合物,得到含水萃余液第三混合物和含己内酰胺和提取剂的有机相第四混合物,其中提取剂是沸点高于己内酰胺的沸点的烷基苯酚; (d)通过蒸馏从有机相第四混合物中回收己内酰胺; (e)将含水萃余液第三混合物再循环到步骤(a)。

    自重排混合物中回收己內醯胺之系統與方法
    134.
    发明专利
    自重排混合物中回收己內醯胺之系統與方法 有权
    自重排混合物中回收己内酰胺之系统与方法

    公开(公告)号:TWI349662B

    公开(公告)日:2011-10-01

    申请号:TW097122056

    申请日:2008-06-13

    Inventor: 李建憲

    IPC: C07D B01J

    CPC classification number: C07D201/16 C07D201/12

    Abstract: 一種自重排混合物中回收己內醯胺之系統與方法,該系統包含中和單元;用以接收由該中和單元饋入之雜質含量低於標準值之粗醯胺溶液的緩衝單元;用以接收由該中和單元饋入之雜質含量高於標準值之粗醯胺溶液的暫存單元;用以進行批次式萃取並分離出第一醯胺溶液的暫時萃取單元;用以進行連續式萃取並分離出第二醯胺溶液的萃取單元;以及用以回收己內醯胺的回收單元。該系統係先根據粗醯胺溶液之品質分別將粗醯胺溶液饋入萃取單元進行連續式萃取或饋入暫時萃取單元進行批次式萃取,藉以維持製程之連續性操作,提高分離效率,減少原物料損耗,同時降低後續純化步驟之負荷。

    Abstract in simplified Chinese: 一种自重排混合物中回收己内酰胺之系统与方法,该系统包含中和单元;用以接收由该中和单元馈入之杂质含量低于标准值之粗酰胺溶液的缓冲单元;用以接收由该中和单元馈入之杂质含量高于标准值之粗酰胺溶液的暂存单元;用以进行批次式萃取并分离出第一酰胺溶液的暂时萃取单元;用以进行连续式萃取并分离出第二酰胺溶液的萃取单元;以及用以回收己内酰胺的回收单元。该系统系先根据粗酰胺溶液之品质分别将粗酰胺溶液馈入萃取单元进行连续式萃取或馈入暂时萃取单元进行批次式萃取,借以维持制程之连续性操作,提高分离效率,减少原物料损耗,同时降低后续纯化步骤之负荷。

    VERFAHREN ZUR HERSTELLUNG VON CAPROLACTAM AUS 6-AMINOCAPRONITRIL
    137.
    发明授权
    VERFAHREN ZUR HERSTELLUNG VON CAPROLACTAM AUS 6-AMINOCAPRONITRIL 失效
    用于生产己内酰胺OFF 6-氨基己腈

    公开(公告)号:EP0912508B1

    公开(公告)日:2002-01-16

    申请号:EP97935513.8

    申请日:1997-07-07

    CPC classification number: C07D201/12 C07D201/08

    Abstract: The invention concerns the preparation of caprolactam by cyclizing 6-aminocapronitrile in the presence of water at high temperature and optionally of a catalyst and a solvent by: a) separating from the reaction yield ('reaction yield I') of the cyclizing process caprolactam and all the components boiling higher than caprolactam ('high boilers'); b) treating the high boilers from step a) with phosphoric acid and/or polyphosphoric acid at a temperature ranging from 200 to 350 °C, obtaining reaction yield II; and c) separating the caprolactam resulting from reaction yield II of step b) and optionally 6-aminocapronitrile from unreacted 'high boilers' and the acid used.

    A PROCESS FOR RECOVERING CAPROLACTAM AND STEAM
    138.
    发明公开
    A PROCESS FOR RECOVERING CAPROLACTAM AND STEAM 有权
    恢复己内酰胺和蒸汽的方法

    公开(公告)号:EP1154995A2

    公开(公告)日:2001-11-21

    申请号:EP00905450.3

    申请日:2000-02-09

    Applicant: DSM N.V.

    CPC classification number: C07D201/12 C07D201/16

    Abstract: The present invention relates to a process for purifying an impure stream of caprolactam while recovering not only pure caprolactam but also medium-to-high pressure steam. Preferably, the stream of impure or crude caprolactam which comprises at a minimum a substantial portion of water, is obtained from depolymerization of a polyamide-containing composition. The resulting purified caprolactam will have a purity greater than 90 weight percent and the recovered steam will have a temperature sufficiently high to provide a driving force for use with other equipment, for instance, heat exchange equipment.

    Process for the preparation of epsilon-caprolactam
    139.
    发明公开
    Process for the preparation of epsilon-caprolactam 审中-公开
    Verfahren zur Herstellung vonε-己内酰胺

    公开(公告)号:EP1122241A1

    公开(公告)日:2001-08-08

    申请号:EP00200365.5

    申请日:2000-02-03

    Applicant: DSM N.V.

    CPC classification number: C07D201/08 C07D201/12

    Abstract: A process for the preparation of ε-caprolactam starting from 6-aminocaproic acid, 6-aminocaproamide, 6-aminocaproic ester, 6-aminocapronitrile, oligomers or polymers of these compounds or mixtures comprising at least two of these compounds, which process is performed in the presence of N-(5-carboxypentyl)-ε-caprolactam and/or derivative thereof in an amount of less than 50 wt.% and more than 0.1 wt.% (based on the total reaction mixture).

    Abstract translation: 从6-氨基己酸,6-氨基己酰胺,6-氨基己酸酯,6-氨基己腈,这些化合物的低聚物或聚合物或包含这些化合物中的至少两种的混合物制备ε-己内酰胺的方法,该方法在 N-(5-羧戊基) - ε-己内酰胺和/或其衍生物的存在量小于50重量%且大于0.1重量%(基于总反应混合物)。

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