COPRODUCCION DE 6-AMINOCAPRONITRILO Y HEXAMETILENDIAMINA.

    公开(公告)号:MX9803864A

    公开(公告)日:1998-09-30

    申请号:MX9803864

    申请日:1998-05-15

    Applicant: BASF AG

    Abstract: Un proceso para la coproduccion de 6-aminocapronitrilo (ACN) y hexametilendiamina (HMD) mediante el tratamiento de adiponitrilo (ADN) con hidrogeno en presencia de un catalizador que contiene níquel a temperaturas no inferiores a la temperatura ambiente y presion parcial de hidrogeno elevada, en presencia o ausencia de solvente, el cual comprende, después que la conversion basada en ADN y/o la selectividad basada en ACN ha descendido abajo de un valor definido. (a) interrumpir el tratamiento del ADN con hidrogeno deteniendo la alimentacion de ADN y del solvente, si se utiliza, (b) tratar el catalizador de 150 a 400 degree C con hidrogeno utilizando una presion de hidrogeno dentro del rango de 0.1 a 30 MPa y un tiempo de tratamiento dentro del rango de 2 a 48 h, y (c) después continuar la hidrogenacion de ADN con el catalizador tratado de la etapa (b).

    133.
    发明专利
    未知

    公开(公告)号:TR199801491T2

    公开(公告)日:1998-09-21

    申请号:TR9801491

    申请日:1996-05-07

    Applicant: BASF AG

    Abstract: A process for preparing caprolactam by reacting 6-aminocapronitrile with water in the presence of catalysts comprises using a starting mixture of 6-aminocapronitrile and the tetrahydroazepine derivative of the formulaand conducting the reaction in liquid phase in the presence of a heterogeneous catalyst. Also describes a process for preparing said tetrahydroazepine derivative I and its use for preparing caprolactam and polycaprolactam.

    Process for preparing 6-aminocapronitrile

    公开(公告)号:AU4115897A

    公开(公告)日:1998-02-25

    申请号:AU4115897

    申请日:1997-07-23

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP97/03987 Sec. 371 Date Feb. 1, 1999 Sec. 102(e) Date Feb. 1, 1999 PCT Filed Jul. 23, 1997 PCT Pub. No. WO98/05631 PCT Pub. Date Feb. 12, 1998The invention concerns a process for the preparation of 6-aminocapronitrile or 6-aminocapronitrile-hexamethylene diamine mixtures by: a) reacting 5-formylvaleronitrile with ammonia and hydrogen in the presence of hydrogenation catalysts selected from the group consisting of metals or metal compounds rhenium, copper and elements of group VIII of the periodic table of elements, a hydrogenation discharge product being obtained; and b) extracting from the hydrogenation discharge product 6-aminocapronitrile and optionally hexamethylene diamine, provided that the hydrogenation catalyst does not contain copper, nickel or copper and nickel as it's only components.

    139.
    发明专利
    未知

    公开(公告)号:BR9607257A

    公开(公告)日:1997-12-30

    申请号:BR9607257

    申请日:1996-02-10

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP96/00578 Sec. 371 Date Aug. 5, 1997 Sec. 102(e) Date Aug. 5, 1997 PCT Filed Feb. 10, 1996 PCT Pub. No. WO96/26198 PCT Pub. Date Aug. 29, 1996Preparation of epoxides from olefins by means of aromatic peroxycarboxylic acids comprises a step A of epoxidizing the olefin and removing the resulting aromatic carboxylic acid from the epoxide, a step B of catalytically hydrogenating the removed aromatic carboxylic acid to the corresponding aromatic aldehyde, and a step C of oxidizing this aldehyde with oxygen or an oxygen-containing gas mixture back to the aromatic peroxycarboxylic acid for re-use for epoxidizing an olefin.

    METHOD OF SIMULTANEOUSLY OBTAINING CAPROLAKTAM AND HEXAMETHYLENEDIAMINE

    公开(公告)号:PL321267A1

    公开(公告)日:1997-11-24

    申请号:PL32126795

    申请日:1995-12-22

    Applicant: BASF AG

    Abstract: The invention concerns the simultaneous preparation of caprolactam and hexamethylene diamine from adipodinitrile, by the following steps: (a) the adipodinitrile is partially hydrogenated, producing a mixture substantially containing 6-aminocapronitrile, hexamethylene diamine, ammonia, adipodinitrile and hexamethylene imine (= "the mixture"); (b) the mixture obtained in step (a) is distilled, producing ammonia, as the forerunnings, and a residue I, in the presence of a compound A which is inert in the distillation conditions, the ammonia not being separated totally; (c) the residue I, substantially containing "the mixture", inert compound A and ammonia, the ammonia content being less than that of the mixture used in step (b), is subjected to a second distillation, producing a mixture of the inert compound A and ammonia, as the forerunnings, and a residue II; (d) the base II, substantially containing "the mixture" and inert compound A, is subjected to distillation in a third column, producing the inert compound A, as the forerunnings, and a residue III; (e) the base III, substantially containing "the mixture" and optionally an inert compound B, is subjected to distillation in a fourth column, producing forerunnings KP1, which substantially contain hexamethylene imine, optionally inert compound B and hexamethylene diamine, and a residue IV; (f) the forerunnings KP1 are subjected in a fifth column to distillation, producing forerunnings KP2, which substantially contain hexamethylene imine and optionally inert compound B, and a residue V, which substantially contains hexamethylene diamine with a degree of purity of at least 95 %, the forerunnings KP2 being fed to the third column or optionally only partially fed to the third column, and the rest being discarded; and (g) the residue IV, substantially containing 6-aminocapronitrile and adipodinitrile, is subjected in a sixth column to distillation, producing 6-aminocapronitrile with a degree of purity of at least 95 %, as forerunnings, and adiponitrile in the residue. The resultant 6-aminocapronitrile is cyclized to form caprolactam.

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