Abstract:
A process for preparing acrylic acid, in which heterogeneously catalyzed gas phase partial oxidation of at least one C3 precursor of acrylic acid with molecular oxygen over catalysts in the solid state of matter at elevated temperature affords a product gas mixture comprising acrylic acid, water vapor and secondary components, then the product gas mixture is directed into a condensation column equipped with separating internals, the product gas mixture is allowed to ascend into itself within the condensation column and undergoes fractional condensation, separating the product gas mixture into a bottoms liquid comprising conversion products and secondary components that are higher-boiling than acrylic acid, a crude acrylic acid comprising water and secondary components that have been depleted overall as target product, an acid water still comprising acrylic acid and secondary components, and a residual gas mixture comprising secondary components that are lower-boiling than water, the target product is conducted out of the condensation column via a side draw and the side draw is above the feed point of the product gas mixture into the condensation column, wherein the parts of the condensation column that are in contact with product are made of stainless steel, at least one of the streams of matter fed to the condensation column comprises a source for halide ions, and halide ions are removed in the region of the separating internals of the condensation column above the side draw.
Abstract:
The present invention relates to a method for transporting a liquid F by means of a pump P, wherein the liquid F comprises at least 10% by weight of a (meth)acrylic monomer, the pump P has a pump space (3), the pump space (3) comprises at least one transport element (4) for transporting the liquid F, the transport element (4) is connected to a drive shaft (6) in such a way that the drive shaft (6) can transmit a torque to the transport element (4), the mounting of the drive shaft is effected by means of at least two sliding bearings (5) in the pump space (3) and the sliding bearings (5) are composed of tungsten carbide.
Abstract:
A plant (1) for recovering acrylic acid, which includes: a absorption column (201); a dissociation column (205); a first line (101) connected to the dissociation column (205); a second line (102) connecting the absorption column (201) and the dissociation column (205); a third line (103) feeding a substream of the mother acid obtained in the crystallization into the dissociation column (205); a fourth line (104) connecting the crystallization apparatus and the absorption column (201); and a fifth line (105) connecting the dissociation column (205) and the absorption column (201).
Abstract:
Process for producing a multimetal oxide catalyst comprising molybdenum, chromium and at least one further metal by mixing of a pulverulent multimetal oxide comprising molybdenum and at least one further metal but no chromium with pulverulent chromium(III) oxide and thermal treatment of the resulting pulverulent mixture in the presence of oxygen at a temperature in the range from 350° C. to 650° C.
Abstract:
The present invention relates to a chimney tray (3) for a column (1) for thermal treatment of fluid mixtures, comprising a collecting tray (4) and at least two chimneys (5-1, 5-2) spaced apart horizontally in the collecting tray (4), where each chimney (5-1, 5-2) forms a vertically aligned chimney body (6-1, 6-2) which forms a passage orifice (7-1, 7-2) through the collecting tray (4), and has a cover unit (8-1, 8-2) arranged spaced apart from the chimney body (6-1, 6-2), and where the cover unit (8-1, 8-2) covers the respective passage orifices (7-1, 7-2) in the vertical direction. The chimney tray (3) of the invention is characterized by a screen (9) which extends around the chimney body (6-1) of a first chimney (5-1), with the lower annular edge (14) of the screen (9) below the upper edge (13) of the chimney body (6-1) of the first chimney (5-1) and the upper annular edge (11) of the screen (9) above the lower outer edge (12) of the cover unit (8-1) of the first chimney (5-1) or adjoining the lower outer edge (12) of the cover unit (8-1) of the first chimney (5-1).
Abstract:
The present invention relates to an extraction column 1 having a vertically aligned column body 2 which is cylindrical at least in sections and forms a column cavity 3 having a horizontal maximum extent, with provision in the column body 2 of at least one first feed 4 for an extractant, at least one second feed 5 for the fluid to be extracted and at least one outlet 6 for the extract mixture and at least one outlet for the raffinate. In the inventive extraction column 1, a vertically aligned divider 7 arranged within the column cavity 3 subdivides the column cavity 3 into a plurality of vertically aligned and horizontally divided regions, the horizontal maximum extent of each region being less than the horizontal maximum extent of the column cavity 3. The invention further relates to a process for extracting a constituent from a fluid by means of such an extraction column 1.
Abstract:
An α,β-unsaturated aldehyde and/or an α,β-unsaturated carboxylic acid are prepared by gas phase oxidation of alkene with molecular oxygen over a fixed catalyst bed comprising a bed of hollow cylindrical shaped catalyst bodies having a multimetal oxide active composition. The fixed catalyst bed comprises at least three successive reaction zones; the highest local temperature in the fixed catalyst bed does not occur in the reaction zone closest to the reactor outlet; the highest local temperature in the fixed catalyst bed does not occur in the reaction zone closest to the reactor inlet; and the value WT=(ED−ID)/2 in the reaction zone in which the highest local temperature in the fixed catalyst bed occurs is lower than in the other reaction zones, in which ED is the external diameter and ID is the internal diameter of the shaped catalyst body. The yield of the products of value is enhanced in this way.
Abstract:
The present invention relates to a process for shutting-down a tubular reactor (1) for a catalytic gas phase reaction from a reaction temperature, wherein the tubular reactor (1) comprises a plurality of vertically arranged reaction tubes (2), an upper tube sheet (5) and a lower tube sheet (6) which each are connected to upper ends and lower ends of the reaction tubes (2) in a gas-tight manner, and a reactor shell (7) which encloses the plurality of reaction tubes (2) forming a liquid-tight heat transfer space (9), wherein, in operation mode, a substantially anhydrous liquefied salt melt (8) is circulated in the heat transfer space (9), characterized in that water (10) is added to the substantially anhydrous liquefied salt melt (8), obtaining a water-salt mixture (11), while cooling the tubular reactor (1) to a temperature below the solidification temperature of the substantially anhydrous liquefied salt melt (8), such that the water-salt mixture (11) is kept in a liquefied state during the whole cooling step of the tubular reactor (1).
Abstract:
Process for preparing butadiene from n-butenes, which has a start-up phase and an operating phase and the operating phase of the process comprises the steps: A) provision of a feed gas stream a1 comprising n-butenes; B) introduction of the feed gas stream a1 comprising n-butenes, an oxygen-comprising gas stream a2 and an oxygen-comprising recycle gas stream d2 into at least one oxidative dehydrogenation zone and oxidative dehydrogenation of n-butenes to butadiene, giving a product gas stream b comprising butadiene; C) cooling and compression of the product gas stream b, giving at least one aqueous condensate stream c1 and a gas stream c2 comprising butadiene; D) introduction of the gas stream c2 into an absorption zone and separation of incondensable and low-boiling gas constituents as gas stream d from the gas stream c2 by absorption of the C4 hydrocarbons in an absorption medium, giving an absorption medium stream loaded with C4 hydrocarbons and the gas stream d, and recirculation of the gas stream d as recycle gas stream d2 to the oxidative dehydrogenation zone, where the start-up phase comprises the steps, in the order i) to iv): i) introduction of a gas stream d2′ having a composition corresponding to the recycle gas stream d2 in the operating phase into the dehydrogenation zone and setting of the recycle gas stream d2 to at least 70% of the total volume flow in the operating phase; ii) optionally additional introduction of a steam stream a3 into the dehydrogenation zone; iii) additional introduction of the feed gas stream a1 comprising butenes at a lower volume flow than in the operating phase and raising of this volume flow until at least 50% of the volume flow of the feed gas stream a1 in the operating phase has been attained, with the total gas flow through the dehydrogenation zone corresponding to not more than 120% of the total gas flow during the operating phase; iv) additional introduction, when at least 50% of the volume flow of the feed gas stream a1 comprising butenes in the operating phase has been attained, of an oxygen-comprising stream a2 at a lower volume flow than in the operating phase and raising of the volume flows of the feed gas streams a1 and a2 until the volume flows in the operating phase have been attained, with the total gas flow through the dehydrogenation zone corresponding to not more than 120% of the total gas flow during the operating phase.