Abstract:
The present invention relates to a column (1) for a thermal treatment of a mixture of compounds having a tendency to polymerization. The column (1) comprises a mass transfer tray (5) comprising a rising tube (8) having an inlet opening (9) below and an outlet opening (10) above the mass transfer tray (5). The rising tube (8) further comprises a lateral opening (11) above the mass transfer tray close to the upper surface of the mass transfer tray (5). Said rising tube (8) is adapted to form a fountain (13) at the outlet opening (10) by atomization of a liquid fraction of the mixture of compounds from the mass transfer tray that enters through the lateral opening into the rising tube (8). The fountain (13) is sprayed to a spot (16) of the column (1) where polymerization is likely to occur. Furthermore, the present invention relates to a thermal separating process that uses such column (1).
Abstract:
The invention relates to a process for preparing acrylic acid from formaldehyde and acetic acid, comprising (i) providing a gaseous stream S1 comprising formaldehyde, acetic acid and acrylic acid, where the molar ratio of acrylic acid to the sum total of formaldehyde and acetic acid in stream S1 is in the range from 0.005:1 to 0.3:1; (ii) contacting stream S1 with an aldol condensation catalyst in a reaction zone to obtain a gaseous stream S2 comprising acrylic acid.
Abstract:
The present invention relates to a process for preparing cyclohexane from methylcyclopentane (MCP) and benzene. In the context of the present invention, MCP and benzene are constituents of a hydrocarbon mixture (HM1) additionally comprising dimethylpentanes (DMP), possibly cyclohexane and possibly at least one compound (low boiler) selected from acyclic C5-C6-alkanes and cyclopentane. First of all, benzene is converted in a hydrogenation step to cyclohexane (that present in the hydrocarbon mixture (HM2)), while MCP is isomerized in the presence of a catalyst, preferably of an acidic ionic liquid, to cyclohexane. After the hydrogenation but prior to the isomerization the dimethylpentanes (DMP) are removed, with initial removal of the cyclohexane present in the hydrocarbon mixture (HM2) together with DMP. This cyclohexane already present prior to the isomerization can be separated again from DMP in a downstream rectification step and isolated and/or recycled into the process for cyclohexane preparation. Between the DMP removal and MCP isomerization—if low boilers are present in the hydrocarbon mixture (HM1)—low boilers are, optionally removed. After the isomerization, the cyclohexane is isolated, optionally with return of unisomerized MCP and optionally of low boilers. Preferably, cyclohexane and/or low boilers are present in the hydrocarbon mixture (HM1), and so a low boiler removal is preferably conducted between the DMP removal from isomerization. It is additionally preferable that the removal of the cyclohexane from DMP is additionally conducted, meaning that the cyclohexane component which arises in the benzene hydrogenation and may be present in the starting mixture (HM1) is isolated and hence recovered.
Abstract:
A process for the continuous production of either acrolein or acrylic acid as the target product from propene comprising a catalyzed gas phase partial oxidation of propene to yield a product gas containing the target product, transferring the target product in a separating zone from the product gas into the liquid phase and conducting out of the separating zone a stream of residual gas the major portion of which is returned into the partial oxidation and the remaining portion of said stream is purged from the process as off-gas from which synthesis gas can be produced or which can be added to synthesis gas produced otherwise.
Abstract:
A process for obtaining acrylic acid, comprising (a) providing a liquid stream S7 comprising acetic acid and acrylic acid, where the molar ratio of acetic acid to acrylic acid in stream S7 is greater than 1:1, (b-1) crystallizing a portion of the acetic acid present in stream S7 to obtain solid crystallized acetic acid in its mother liquor, (b-2) separating the mother liquor from the acetic acid crystallized in (b-1) to obtain the solid crystallized acetic acid and a liquid stream S8 comprising acrylic acid and acetic acid, (c) separating stream S8 into at least one stream S10 depleted of acrylic acid compared to S8 and a stream S11 enriched in acrylic acid compared to S8.
Abstract:
The invention relates to a process for preparing acrylic acid from formaldehyde and acetic acid, comprising (i) providing a gaseous stream S1 comprising formaldehyde, acetic acid, oxygen and water, where the formaldehyde content of stream S1 is in the range from 8% to 18% by volume, based on the total volume of stream S1, the ratio of the volumes of acetic acid to formaldehyde is in the range from 0.6:1 to 1.1:1, and the molar ratio of oxygen to the total amount of organic carbon is in the range from 0.02:1 to 0.15:1; (ii) contacting stream S1 with an aldol condensation catalyst in a reaction zone to obtain a gaseous stream S2 comprising acrylic acid.
Abstract:
An oxidic composition comprising vanadium, tungsten, phosphorus, oxygen and optionally tin, where the molar ratio of phosphorus to the sum total of vanadium, tungsten and any tin in the oxidic composition is in the range from 1.4:1 to 2.4:1.
Abstract:
A process for preparing acrylic acid from methanol and acetic acid, comprising (i) contacting a gaseous stream S0 comprising methanol, oxygen and inert gas with an oxidation catalyst to obtain a gaseous stream S1 comprising formaldehyde and inert gas; (ii) removing at least a portion of the inert gas present in S1 from at least a portion of the formaldehyde present in S1 by absorbing this formaldehyde in an absorbent to obtain a gaseous stream S2 comprising the portion of the inert gas removed, and to obtain a stream S3 comprising absorbent and absorbate comprising formaldehyde; (iii) optionally removing a portion or the entirety of the absorbent present in stream S3, such that a stream S3a remains from stream S3, and producing a stream S4 from at least stream S3 or stream S3a and a stream S5 comprising acetic acid; and (iv) contacting stream S4 in gaseous form with an aldol condensation catalyst to obtain a gaseous stream S6 comprising acrylic acid.