PROCESS FOR THE PREPARATION OF PROPYLENE OXIDE

    公开(公告)号:CA1097367A

    公开(公告)日:1981-03-10

    申请号:CA264296

    申请日:1976-10-27

    Applicant: BAYER AG DEGUSSA

    Abstract: PROCESS FOR THE PREPARATION OF PROPYLENE OXIDE Process for continuous production of propylene oxide (Fig. 1) from propylene and aqueous hydrogen peroxide. The aqueous hydrogen peroxide is first reacted with propionic acid in the presence of acid catalyst to form perpropionic acid (1). The perpropionic acid is taken up by extraction in benzene (5); the perpropionic acid in the benzene solution is reacted with propylene (21) for oxidation of the propylene to propylene oxide and conversion of the perpropionic acid back to propionic acid. The reaction mixture is worked up to separate propylene oxide, propionic acid and benzene (27, 29, 34, 37), and the latter two are recyled. In the benzene extraction (5), an aqueous raffinate (7) is formed containing hydrogen peroxide and acid catalyst. The aqueous raffinate can be divided into a stream which is recycled to the propionic acid reactor (1), and a second stream which can be distilled to remove water with the concentrate being recycled to the propionic acid reactor. (1) Le A 17,343/6142 PV -1-

    43.
    发明专利
    未知

    公开(公告)号:DD146047A5

    公开(公告)日:1981-01-21

    申请号:DD21572079

    申请日:1979-09-21

    Applicant: DEGUSSA

    Abstract: The residual gases obtained in the production of cyanuric chloride having a pressure of 1-5 bar (absolute) preferably 1-4 bar, are worked up by leading them into the lower portion of a column, reacted in the column with at least the equivalent amount of hydrogen cyanide to form cyanogen chloride and led in countercurrent flow to the water charged to the upper portion of the column whereupon the aqueous solution of cyanogen chloride formed is withdrawn from the lower portion of the column and preferably is returned into the production portion of the plant for recovery of the cyanogen chloride while the purified waste gas of the column leaves in the upper portion of the column.

    44.
    发明专利
    未知

    公开(公告)号:RO67635A

    公开(公告)日:1980-04-15

    申请号:RO7210572

    申请日:1972-09-01

    Applicant: DEGUSSA

    Abstract: N-alkyl formamides or the corresponding N-cycloalkyl or N-aralkyl formamaides are prepared by reacting olefins, cycloolefins or aralkenes with hydrogen cyanide in the Ritter reaction using about 2.5 moles of acid per mole of olefin at a temperature of 30 DEG to 70 DEG C. and the unneutralized acid reaction mixture is extracted with acid stable polar solvents and the extract is worked up in conventional manner.

    PROCESS FOR PRODUCING CYANOGEN CHLORIDE (I)

    公开(公告)号:CA1074529A

    公开(公告)日:1980-04-01

    申请号:CA252040

    申请日:1976-05-07

    Applicant: DEGUSSA

    Abstract: The present invention provides in a process for producing cyanogen chloride by reacting hydrogen cyanide with hydrogen chloride or hydrochloric acid and hydrogen peroxide in an aqueous medium in the presence of cupric and ferric ions, the improvement in which the reaction is carried out under superatmospheric pressure and that cyanogen chloride is recovered separately from oxygen and nitrogen.

    49.
    发明专利
    未知

    公开(公告)号:RO66454A

    公开(公告)日:1979-01-15

    申请号:RO8085074

    申请日:1974-12-18

    Applicant: DEGUSSA

    Abstract: Cyanogen chloride is purified and the service life of activated carbon is increased in the subsequent trimerization of the cyanogen chloride to cyanuric chloride by process comprising reacting hydrogen cyanide with chlorine, in a given case in the presence of cyanogen chloride produced in the presence of water, which in a given case contains chlorine. The improvement comprises passing the cyanogen chloride over granular gamma aluminum oxide with an alkali metal or in a given case an alkaline earth metal content of 0 to 3 weight % at 20 DEG -100 DEG C., preferably 30 DEG -60 DEG C.

    50.
    发明专利
    未知

    公开(公告)号:CH607985A5

    公开(公告)日:1978-12-15

    申请号:CH1711174

    申请日:1974-12-20

    Applicant: DEGUSSA

    Abstract: Cyanogen chloride is purified and the service life of activated carbon is increased in the subsequent trimerization of the cyanogen chloride to cyanuric chloride by process comprising reacting hydrogen cyanide with chlorine, in a given case in the presence of cyanogen chloride produced in the presence of water, which in a given case contains chlorine. The improvement comprises passing the cyanogen chloride over granular commercial sodium aluminum silicate or a molecular sieve of the mordenite type, at 20 DEG -100 DEG C., preferably 30 DEG -60 DEG C.

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