22.
    发明专利
    未知

    公开(公告)号:AT403658T

    公开(公告)日:2008-08-15

    申请号:AT05740694

    申请日:2005-05-13

    Applicant: BASF SE

    Abstract: Process for preparing a solution of pure triethylenediamine (TEDA), in which TEDA is vaporized, the gaseous TEDA is passed into a liquid solvent 1 (quench) and the TEDA is crystallized from the resulting solution and separated off (solid-liquid separation), wherein the crystalline TEDA obtained is dissolved in a solvent 2 and a stripping gas is passed through the resulting solution (stripping).

    Dispositivo para llevar a cabo procesos de intercambio de sustancias

    公开(公告)号:ES2990013T3

    公开(公告)日:2024-11-28

    申请号:ES21732904

    申请日:2021-06-17

    Applicant: BASF SE

    Abstract: La invención se refiere a un dispositivo para llevar a cabo procesos de intercambio de material, que comprende una columna con al menos dos conectores para el suministro de una fase vaporosa, en la que se alojan componentes separables en la columna y una sección de columna se extiende desde los al menos dos conectores hasta los componentes separables, en la que está cubierta menos del 25 % de una sección transversal de la columna, con respecto a la sección transversal total, y en la que los al menos dos conectores presentan un desfase en altura correspondiente a un máximo de tres veces el diámetro del conector, y los al menos dos conectores forman un ángulo (α) entre sí de 60° a 150° y son asimétricos entre sí. La invención se refiere también a un uso del dispositivo y a un procedimiento para diseñar el dispositivo. (Traducción automática con Google Translate, sin valor legal)

    METHOD FOR PRODUCING 2-OCTYL (METH)ACRYLATE

    公开(公告)号:AU2022395238A1

    公开(公告)日:2024-06-06

    申请号:AU2022395238

    申请日:2022-11-14

    Applicant: BASF SE

    Abstract: The invention relates to a method for preparing 2-octyl (meth)acrylate by reacting 2-octanol with (meth)acrylic acid in the presence of an acidic esterification catalyst, a polymerisation inhibitor and the entrainer cyclohexane, the method comprising the following steps: • providing a reactor unit (24), a reactor (1) with a reactor heating element (30) being located inside the reactor unit (24), • feeding 2-octanol (13), (meth)acrylic acid (14), acidic esterification catalyst (15), cyclohexane (17) and polymerisation inhibitor (31) into the reactor (1), • performing an esterification in the reactor (1) so as to form a liquid reaction mixture, the esterification taking place in the reactor (1) at a sump temperature in the range from 90 to 130°C and at an absolute pressure in the range of 0.5 to 2.0 bar, and a resultant reaction output from the reactor (1) being obtained, the resultant reaction output containing at least 2-octyl (meth)acrylate, 2-octanol, (meth)acrylic acid, acidic esterification catalyst, cyclohexane, esterification water and polymerisation inhibitor, and the esterification water created during the esterification forming, together with the entrainer cyclohexane, a heterogeneous azeotrope, • evaporating the heterogeneous azeotrope from the liquid reaction mixture of the reactor (1), the evaporation being achieved by the reactor heating element (30), and • separating off the gaseous heterogeneous azeotrope from the reactor (1), the gaseous heterogeneous azeotrope being condensed in a condenser (5) and then fed to a phase separator (6), and the esterification water being separated off as lower phase and the cyclohexane being separated off as upper phase in this phase separator (6).

    METHOD FOR PRODUCING 2-OCTYL (METH)ACRYLATE

    公开(公告)号:CA3240124A1

    公开(公告)日:2023-06-01

    申请号:CA3240124

    申请日:2022-11-14

    Applicant: BASF SE

    Abstract: The invention relates to a method for preparing 2-octyl (meth)acrylate by reacting 2-octanol with (meth)acrylic acid in the presence of an acidic esterification catalyst, a polymerisation inhibitor and the entrainer cyclohexane, the method comprising the following steps: providing a reactor unit (24), a reactor (1) with a reactor heating element (30) being located inside the reactor unit (24), feeding 2-octanol (13), (meth)acrylic acid (14), acidic esterification catalyst (15), cyclohexane (17) and polymerisation inhibitor (31) into the reactor (1), performing an esterification in the reactor (1) so as to form a liquid reaction mixture, the esterification taking place in the reactor (1) at a sump temperature in the range from 90 to 130°C and at an absolute pressure in the range of 0.5 to 2.0 bar, and a resultant reaction output from the reactor (1) being obtained, the resultant reaction output containing at least 2-octyl (meth)acrylate, 2-octanol, (meth)acrylic acid, acidic esterification catalyst, cyclohexane, esterification water and polymerisation inhibitor, and the esterification water created during the esterification forming, together with the entrainer cyclohexane, a heterogeneous azeotrope, evaporating the heterogeneous azeotrope from the liquid reaction mixture of the reactor (1), the evaporation being achieved by the reactor heating element (30), and separating off the gaseous heterogeneous azeotrope from the reactor (1), the gaseous heterogeneous azeotrope being condensed in a condenser (5) and then fed to a phase separator (6), and the esterification water being separated off as lower phase and the cyclohexane being separated off as upper phase in this phase separator (6).

    PROCESS FOR ISOLATING PURE TERT-BUTYL (METH)ACRYLATE FROM CRUDE TERT-BUTYL (METH)ACRYLATE BY DISTILLATION

    公开(公告)号:MY191514A

    公开(公告)日:2022-06-28

    申请号:MYPI2019003354

    申请日:2017-12-11

    Applicant: BASF SE

    Abstract: A process for isolating pure tert-butyl (meth)acrylate from crude tert-butyl (meth)acrylate by distillation, wherein the process is carried out in a dividing wall column (1) having separation-active internals and a vaporizer (7) and in which a dividing wall (8) is arranged in the longitudinal direction of the column to form an upper joint column region (9), a lower joint column region (14), an inflow section (10, 12) having a side feed point (2), and an offtake section (11, 13) having a side offtake point (3), where the column has from 20-80 theoretical plates and the ratio of the amount of liquid at the upper end of the dividing wall (8) going to the enrichment section (10) and the stripping section (11) of the column is set in the range from 1:0.2 to 1:5. (Fig.1)

    PROCESS FOR CONTINUOUSLY PREPARING N-BUTYL ACRYLATE OR ISOBUTYL ACRYLATE

    公开(公告)号:CA3070757A1

    公开(公告)日:2019-02-21

    申请号:CA3070757

    申请日:2018-08-13

    Applicant: BASF SE

    Abstract: The invention relates to a method for continuously producing an acrylic acid butyl ester H2C=CH-C(=O)OR, with R = n-butyl or isobutyl, wherein aqueous 3-hydroxypropionic acid is reacted under dehydrating and esterifying conditions in the presence of the corresponding butanol R-OH in a reactor with a rectification column and the formed acrylic acid butyl ester, unreacted butanol and introduced and formed water are distilled off at the top as a ternary azeotrope, after separation into a liquid aqueous phase and a liquid organic phase the aqueous phase and the organic phase are each at least partially ejected, and the organic phase, containing the acrylic acid butyl ester and the butanol, is separated by distillation.

    Procedimiento para la preparación de una solución de formaldehído altamente concentrada

    公开(公告)号:ES2485309T3

    公开(公告)日:2014-08-13

    申请号:ES05715282

    申请日:2005-02-10

    Applicant: BASF SE

    Abstract: Procedimiento para la preparación de una solución de formaldehído altamente concentrada mediante separación de agua de una solución de formaldehído de menor concentración con un contenido de formaldehído entre el 5 % y el 50 % en peso, en el que se suministra la solución de formaldehído de menor concentración a un precalentador y se calienta en el precalentador, se relaja a través de un dispositivo de mantenimiento de presión y se concentra en un evaporador de tubo helicoidal con obtención de una corriente de vaho así como de la solución de formaldehído altamente concentrada como corriente de fondo, caracterizado porque se relaja la solución de formaldehído de menor concentración calentada en el dispositivo de mantenimiento de presión hasta dar una mezcla bifásica que se suministra al evaporador de tubo helicoidal.

    29.
    发明专利
    未知

    公开(公告)号:DE502006000740D1

    公开(公告)日:2008-06-19

    申请号:DE502006000740

    申请日:2006-07-26

    Applicant: BASF SE

    Abstract: Continuous distillative separation of piperazine from ethylenediamine-piperazine mixture comprises subjecting the piperazine mixture into a cyclic motion, introducing the piperazine mixture into an evaporator unit at 160-170[deg]C, recycling the piperazine mixture into a distillation column and removing the piperazine from the sump of the distillation column after a retention time of approximately 30-60 minutes, where the ethylene diamine is discharged at the upper portion of the distillation column.

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