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公开(公告)号:FR1462866A
公开(公告)日:1966-12-16
申请号:FR44939
申请日:1966-01-05
Applicant: BASF AG
Inventor: SLIWKA WOLFGANG , HEIL EDUARD
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公开(公告)号:DE3515516A1
公开(公告)日:1986-11-06
申请号:DE3515516
申请日:1985-04-30
Applicant: BASF AG
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公开(公告)号:CA1205594A
公开(公告)日:1986-06-03
申请号:CA407664
申请日:1982-07-20
Applicant: BASF AG
Inventor: HINSELMANN KLAUS , NAARMANN HERBERT , ECHTE ADOLF , HEIL EDUARD , NIKLES ALBERT , REFFERT RUDI W , HAMBRECHT JUERGEN
IPC: C08L7/00 , B29C35/00 , B29C45/00 , C08G65/46 , C08J3/00 , C08J3/20 , C08L21/00 , C08L23/00 , C08L33/00 , C08L33/02 , C08L71/00 , C08L71/12 , C08L101/00 , C08L71/04 , C08L25/04 , C08L51/04
Abstract: Molding materials containing high molecular weight polyphenylene ethers are produced by a process in which a solution of a polyphenylene ether in an organic solvent, together with another polymer, is freed of solvent by multi-stage evaporation. The solvent is preferably an aromatic compound from the class comprising the hydrocarbons, halohydrocarbons, ethers or esters, the ratio of the other polymer to the polyphenylene ether is advantageously from 99 : 1 to 20 : 80 parts by weight, the other polymer is, in particular, a homopolymer or copolymer of styrene or of a homolog thereof, which may be modified with rubber, and the multi-stage evaporation process preferably comprises not less than two and not more than four workingup stages. The evaporation is carried out in general at from 120 to 280.degree.C and under a pressure of from 1 to 3,000 mbar, advantageously in the presence of assistants which reduce the partial pressure, eg. water and/or methanol.
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公开(公告)号:AT19409T
公开(公告)日:1986-05-15
申请号:AT82106328
申请日:1982-07-15
Applicant: BASF AG
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公开(公告)号:DE3342178A1
公开(公告)日:1985-05-30
申请号:DE3342178
申请日:1983-11-23
Applicant: BASF AG
Inventor: REFFERT RUDI WILHELM , HAMBRECHT JUERGEN DR , BAER KARL DR , HEIL EDUARD , ECHTE ADOLF DR
IPC: C08G65/46
Abstract: The invention relates to a process for the removal of the metal component of the catalyst from a polyphenylene ether solution produced in the preparation of high-molecular-weight polyphenylene ethers from monohydric phenols by oxidative coupling reaction with oxygen in the presence of a catalyst complex comprising a metal salt and an organic amine in the presence of a solvent and optionally an activator, by treatment with a precipitant which is a solid chemical reagent which is insoluble in the polyphenylene ether solution, and has been applied to an inert support substance which is adsorbent with respect to the precipitated substances. The precipitant is an organic P-, S-, O- or N-containing compound or an inorganic P or S compound which is soluble in water or aqueous acid solution, the support substance is a solid material of any desired shape with a specific surface area of from 50 to 1500 m /g and a porosity of between 50 and 75% which is insoluble in water, acid and organic solvents.
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公开(公告)号:DE3315803A1
公开(公告)日:1984-10-31
申请号:DE3315803
申请日:1983-04-30
Applicant: BASF AG
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公开(公告)号:AU7928175A
公开(公告)日:1976-09-23
申请号:AU7928175
申请日:1975-03-19
Applicant: BASF AG
Inventor: MERTES FRIEDERICH , DOERFEL HELMUT , HEIL EDUARD , CORDES CLAUS
Abstract: An improved process for the continuous manufacture of polyamides by continuously conveying the aqueous solution of a salt of essentially equivalent amounts of a diamine, or of a mixture of several diamines, and of a dicarboxylic acid, or of a mixture of several dicarboxylic acids, or of mixtures of such salts with lactams and/or aminocarboxylic acids, through several reaction zones under polyamide-forming conditions, wherein the mixture of starting materials is heated, in a first reaction zone, to from 200 DEG to 300 DEG C, preferably from 220 DEG to 280 DEG C, at pressures which are above the corresponding saturation vapor pressure of water and prevent the formation of a vapor phase, the pressure action on the polycondensation mixture is released in a second reaction zone and condensation of the mixture, to form high molecular weight polyamides, is then completed in further reaction stages. According to the invention, A. THE MIXTURE OF STARTING MATERIALS IS HEATED, IN THE FIRST REACTION ZONE, UNTIL THE POLYCONDENSATION CONVERSION IS AT LEAST 80% AND PREFERABLY 90%, B. IN THE SECOND ZONE THE PRESSURE ACTING ON THE POLYCONDENSATION MIXTURE IS RELEASED, ADIABATICALLY, TO LEVELS OF NOT LESS THAN 3 ATMOSPHERES, PREFERABLY NOT LESS THAN 5 ATMOSPHERES, AND NOT MORE THAN 20 ATMOSPHERES, PREFERABLY NOT MORE THAN 15 ATMOSPHERES, SO AS TO REACH TEMPERATURES BELOW 215 DEG C, preferably 210 DEG C, c. the polycondensation mixture is then heated in a third reaction zone, comprising a heat exchanger consisting of heat exchange elements connected in parallel, to from 220 DEG to 330 DEG C, preferably from 250 DEG to 300 DEG C, in the course of less than 5 minutes and preferably less than 1 minute, the heating being carried out preferably in the presence of the water vapor formed during the adiabatic release of the pressure (in stage b), with application of heat and evaporation of the bulk of the water, at the pressure level to which the pressure has previously been released or at a lower pressure, and D. IN FURTHER REACTION STAGES, THE CONDENSATION IS COMPLETED, UNDER THE CONDITIONS PREVAILING AT THE END OF THE THIRD REACTION ZONE AND, FINALLY, BY CONVENTIONAL METHODS, TO FORM HIGH MOLECULAR WEIGHT POLYAMIDES.
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公开(公告)号:DE3669321D1
公开(公告)日:1990-04-12
申请号:DE3669321
申请日:1986-03-29
Applicant: BASF AG
Inventor: MITULLA KONRAD DR , HAMBRECHT JUERGEN DR , HEIL EDUARD , FISCHER HERMANN DR , DREHER HERMANN DR , BRANDT HERMANN DR , LUETJE HANS DR
IPC: C08G65/44
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公开(公告)号:CA1263992A
公开(公告)日:1989-12-19
申请号:CA495489
申请日:1985-11-15
Applicant: BASF AG
Inventor: BRANDT HERMANN , FISCHER HERMANN , DREHER HERMANN , HEIL EDUARD , HAMBRECHT JUERGEN , NAARMANN HERBERT , ECHTE ADOLF , GAUSEPOHL HERMANN , SIEBEL PETER , SWOBODA JOHANN , SCHWOEBEL GERD , NIKLES ALBERT
Abstract: Disclosed is a process of preparation of polyphenylene ethers from monohydric phenols, which possess alkyl substituents in the two ortho-positions and, if desired, in the meta-position, but not in the para-position, by an oxidative coupling reaction with oxygen at from 15 to 50.degree.C and under from 1 to 10 bar in the presence of a catalyst complex, of a solvent and, if required, of an activator. In this process,the conversion of the phenols is carried out in two or more reaction zones. Some or all of the solvent, catalyst complex phenols and where relevant, activator are initially added to one of the reaction zones and are circulated in the other reaction zone and about 60-100% of the stoichiometric amount of oxygen required for the oxidative coupling is introduced into the first reaction zone and from 0 to about 40% of the said stoichiometric amount is introduced into the second reaction zone. This process is interesting in that it makes it possible to carry out oxidative coupling of phenols with oxygen in a very economic and reliable manner, with very high space-time yields, formation of only a small amount of by-products, and minimum emissions of gas and volatile components.
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公开(公告)号:CA1222590A
公开(公告)日:1987-06-02
申请号:CA456616
申请日:1984-06-14
Applicant: BASF AG
Inventor: PIPPER GUNTER , SCHMIDT FRANZ , THEYSOHN RAINER , RIEGGER SIEGFRIED , HEIL EDUARD , FISCHER HERMANN , THOMA RICHARD , MATTHIES PAUL
Abstract: - 10 - O.Z. 0050/36564 Nylons are prepared by a continuous process in which, in a precondensation zone, an aqueous solution of a salt of a dicarboxylic acid of 6 to 18 carbon atoms and a diamine of 6 to 18 carbon atoms is heated to 250-300.degree.C under superatmospheric pressure, with simultaneous vaporization of water and formation of a prepolymer, the prepolymer and the vapor are separated, and the former is fed into a polycondensation zone and condensed under superatmospheric pressure of from 1 to 10 bar and at from 250 to 300.degree.C, wherein the aqueous salt solution is condensed under superatmospheric pressure of from 1 to 10 bar in the first third of the tubular precondensation zone provided with baffles, until the degree of conversion is not less than 93%, and the prepolymer and the vapor phase are brought into intimate contact with one another in the remaining two thirds of the precondensation zone.
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