3.
    发明专利
    未知

    公开(公告)号:DE2823983A1

    公开(公告)日:1979-12-06

    申请号:DE2823983

    申请日:1978-06-01

    Applicant: BASF AG

    Abstract: A process for isolating 1,3-butadiene by means of a selective solvent from a C4-hydrocarbon mixture which contains 1,3-butadiene, propyne, hydrocarbons which are more soluble than 1,3-butadiene in the selective solvent and hydrocarbons which are less soluble than 1,3-butadiene in the selective solvent, wherein the C4-hydrocarbon mixture is separated, using one or more extractive distillation zones, into a distillate containing the less soluble hydrocarbons, a stream of 1,3-butadiene and a stream containing the more soluble hydrocarbons, and the propyne is separated off either by distillation of the C4-hydrocarbon mixture in a distillation zone upstream of the extractive distillation zone or zones or by distillation of the stream of 1,3-butadiene, obtained from the extractive distillation zone or zones, in a downstream distillation zone, giving a stream of hydrocarbons containing propyne and 1,3-butadiene, which stream is fed to an additional distillation zone, while at the same time a second stream of liquid or gaseous hydrocarbons is fed to the additional distillation zone, and the bottom product from the additional distillation zone is recycled to the extractive distillation.

    4.
    发明专利
    未知

    公开(公告)号:DE2923012A1

    公开(公告)日:1980-12-18

    申请号:DE2923012

    申请日:1979-06-07

    Applicant: BASF AG

    Abstract: A process for simultaneously removing water and hydrogen sulfide from gases containing both of these by treating the gases, in an absorption zone under superatmospheric pressure, with polyethylene glycol dialkyl ethers as a solvent, stripping the hydrogen sulfide from the loaded solvent, obtained from the absorption zone, in a desorption zone, removing the water, taken up in the absorption zone, from the solvent and recycling the regenerated solvent to the absorption zone, wherein the solvent additionally contains from 0.01 to 20% by weight, based on the solvent mixture, of an alcohol or ether boiling in the range from 50 DEG to 140 DEG C.

    5.
    发明专利
    未知

    公开(公告)号:DE2724365A1

    公开(公告)日:1978-11-30

    申请号:DE2724365

    申请日:1977-05-28

    Applicant: BASF AG

    Abstract: A process for separating, by means of a selective solvent, a mixture of C4-hydrocarbons which contains some hydrocarbons which are more soluble in the selective solvent and some which are less soluble therein, in which process the hydrocarbon mixture is separated, in an extractive distillation zone, into a top product which contains the less soluble hydrocarbons and an extract which contains the more soluble hydrocarbons and the selective solvent, the extract, taken off as the bottom product, is subjected to a flash evaporation and the resulting vapor component of the extract is recycled to the extractive distillation zone while the liquid phase remaining after the flash evaporation is fed to a solvent recovery zone, in which the liquid phase obtained from the flash evaporation is separated into a product containing the hydrocarbons and, as the bottom product, the selective solvent which has been freed from the hydrocarbons, the resulting selective solvent is recycled to the extractive distillation zone and the product which is obtained from the solvent recovery zone and contains the hydrocarbons is partially or completely recycled to the extractive distillation zone, after increasing the pressure in a compression zone, in which process the extract taken off the extractive distillation zone is brought, prior to the flash evaporation to a higher pressure than the pressure in the extractive distillation zone and thereafter the extract which is under this higher pressure is heated, in a heat exchange zone, by indirect heat exchange with the selective solvent obtained as the bottom product from the solvent recovery zone, and the heated extract is subsequently let down, in the flash evaporation, to a pressure which is at least equal to the pressure in the extractive distillation zone and is higher than the pressure in the solvent recovery zone.

    6.
    发明专利
    未知

    公开(公告)号:DE3112661A1

    公开(公告)日:1982-10-14

    申请号:DE3112661

    申请日:1981-03-31

    Applicant: BASF AG

    Abstract: A process for removing condensable aliphatic hydrocarbons and acidic gases such as H2S, CO2 and COS from natural gas containing these, wherein the natural gas is initially treated with polyethylene glycol dialkyl ethers, as the solvent, in a first absorption stage to effect absorption of the condensable aliphatic hydrocarbons; the natural gas drawn off from the first absorption stage is then treated with polyethylene glycol dialkyl ethers, as the solvent, under superatmospheric pressure in a second absorption stage, the acidic gases being completely or partly absorbed; the solvent charged with the condensable aliphatic hydrocarbons which is obtained from the first absorption stage is treated with water in an extraction stage, to form a hydrocarbon phase containing the condensable aliphatic hydrocarbons and an aqueous dialkyl ether phase, and the hydrocarbon phase is separated from the aqueous dialkyl ether phase. The solvent charged with acid gases which is obtained from the second absorption stage is regenerated by expansion and/or stripping in a regeneration stage and the regenerated solvent is recycled to the absorption.

    Bubble columns for gas-liquid reactions - with subdividing sieve plates having defined and adjustable openings

    公开(公告)号:DE2634785A1

    公开(公告)日:1978-02-09

    申请号:DE2634785

    申请日:1976-08-03

    Applicant: BASF AG

    Abstract: A reaction column contains intermediate sieve plates whose spacing is less than twice the column dia. and whose total hole area is 10-40% of the column cross-section. Specifically, bubbling type gas-liquid reaction column is subdivided internally by sieve plates which are arranged in a demountable module for easy replacement. Each plate is of double construction so that by relative rotation of the two parts the available hole opening may be adjusted to suit the characteristics of the reacting system. The individual hole dia. is pref. >10mm, and the holes are circular; in a 400 mm i/d column the plate spacing is >=200 mm. Used for continuous chemical reaction between counter-flowing gas and liq. or slurry streams, in columns of dia. >400 mm. Reduces back-mixing effect without the complexity of column packing and without the need for reaction systems in cascade.

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