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    64.
    发明专利
    未知

    公开(公告)号：BR0109882A

    公开(公告)日：2003-06-03

    申请号：BR0109882

    申请日：2001-04-04

    Applicant: BASF AG

    Inventor： GUMBEL HELMUT ,  KAHMAN MARTIN AUS DEM ,  WAGNER NORBERT ,  TAEGER KLAUS

    IPC: C07C43/11 ,  C08G65/06 ,  C08G65/26 ,  C08G65/28 ,  C09K23/42 ,  C11D1/722 ,  C11D3/00 ,  C11D11/00

    Abstract: Alcohol alkoxylates of the formula (I)whereR is an at least singly branched C4-22-alkylR is C3-4-alkylR is C1-4-alkylR is methyl or ethyln is an average value from 1 to 50m is an average value from 0 to 20r is an average value from 0 to 50s is an average value from 0 to 50,where m is at least 0.5 if R is methyl or ethyl or r is 0, or alcohol alkoxylates of the formula (II)whereR is branched or unbranched C4-22-alkylR is C3-4-alkylp is an average value of from 1 to 50q is an average value of from 0.5 to 20are used as low-foam or foam-suppressing surfactants.

    65.
    发明专利
    未知

    公开(公告)号：DE10105030A1

    公开(公告)日：2002-08-08

    申请号：DE10105030

    申请日：2001-02-05

    Applicant: BASF AG

    Inventor： KLUGE MICHAEL ,  HILDEBRANDT SOEREN ,  WAGNER NORBERT ,  WEHLAGE THOMAS

    IPC: C07D223/10 ,  C07D227/087

    Abstract: The invention relates to a method for producing N,N'-carbonylbis- epsilon -caprolactam by the single-stage reaction of epsilon -caprolactam with phosgene, optionally in an inert organic solvent, in the presence of an organic nitrogenous base without an acylable nitrogen atom. The invention is characterised in that the organic nitrogenous base has a pKa-value of between 5 and 7. N,N-dimethylaniline is the preferred nitrogenous base.

    66.
    发明专利
    未知

    公开(公告)号：DE10105029A1

    公开(公告)日：2002-08-08

    申请号：DE10105029

    申请日：2001-02-05

    Applicant: BASF AG

    Inventor： KLUGE MICHAEL ,  HILDEBRANDT SOEREN ,  WAGNER NORBERT ,  WEHLAGE THOMAS

    IPC: C07D201/02 ,  C07D201/16 ,  C07D223/10 ,  C07D227/087 ,  C08G69/14

    Abstract: The invention relates to a method for producing N,N'carbonylbis- epsilon -caprolactam by reacting epsilon -caprolactam with phosgene in the presence of a hydrogen chloride-binding agent in an inert organic solvent and isolating the reaction product from the product solution. The isolation comprises the following steps: a) optionally distilling off a part of the organic solvent from the product solution; b) adding water to the product solution; c) removing the organic solvent by azeotropic distillation, optionally while replacing the water distilled off, thereby deploying the product solution of organic solvent; d) allowing the N,N'-carbonylbis- epsilon -caprolactam to crystallize from the solution that is deployed from organic solvent, thereby obtaining an aqueous suspension of N,N'-carbonylbis- epsilon -caprolactam; and e) removing the crystallized product.

    PROCESS FOR PREPARING NANOPARTICULATE LANTHANOID-BORON COMPOUNDS OR SOLID MIXTURES COMPRISING NANOPARTICULATE LANTHANOID-BORON COMPOUNDS
    69.
    发明专利
    PROCESS FOR PREPARING NANOPARTICULATE LANTHANOID-BORON COMPOUNDS OR SOLID MIXTURES COMPRISING NANOPARTICULATE LANTHANOID-BORON COMPOUNDS 未知

    公开(公告)号：CA2611334C

    公开(公告)日：2013-12-24

    申请号：CA2611334

    申请日：2006-06-14

    Applicant: BASF AG

    Inventor： PROELSS JULIAN ,  BRAMNIK KIRILL ,  WAGNER NORBERT ,  NORDMANN GERO ,  HAMMERMANN MARKUS ,  BENOEHR ALEXANDER

    IPC: C01B35/04 ,  C01B35/00

    Abstract: The present invention relates to a process for preparing essentially isometric nanopar-ticulate lanthanide-boron compounds or solid mixtures comprising essentially isometric nanoparticulate lanthanide-boron compounds, which comprises a) mixing i) one or more lanthanide compounds selected from the group consisting of lanthanide hydroxides, lanthanide hydrides, lanthanide chalcogenides, lantha-nide halides, lanthanide borates and mixed compounds of the lanthanide com-pounds mentioned, ii) one or more compounds selected from the group consisting of crystalline bo-ron, amorphous boron, boron carbides, boron hydrides and boron halides and iii) if appropriate one or more reducing agents selected from the group consisting of hydrogen, carbon, organic compounds, alkaline earth metals and alkaline earth metal hydrides dispersed in an inlet carrier gas with one another, b) reacting the mixture of the components i), ii) and, if appropriate, iii) in the inert solvent by means of thermal treatment within a reaction zone, c) subjecting the reaction product obtained by means of thermal treatment in step b) to rapid cooling and d) subsequently separating off the reaction product which has been cooled in step c), with the cooling conditions in step c) being selected so that the reaction product consists of essentially isometric nanoparticulate lanthanide-boron compounds or comprises essentially isometric nanoparticulate lanthanide-boron compounds.

    AMPHIPHILIC POLYMER COMPOSITIONS AND THEIR USE
    70.
    发明专利
    AMPHIPHILIC POLYMER COMPOSITIONS AND THEIR USE 未知

    公开(公告)号：CA2567660C

    公开(公告)日：2012-05-08

    申请号：CA2567660

    申请日：2005-06-07

    Applicant: BASF AG

    Inventor： OETTER GUNTER ,  KRUGER CHRISTIAN ,  KOHLE HARALD ,  SCHERER MARIA ,  WAGNER NORBERT ,  BRATZ MATTHIAS ,  BERGHAUS RAINER ,  VAN GELDER RICHARD

    IPC: C08G18/62 ,  A01N25/04 ,  A01N25/30 ,  C08G18/28 ,  C08G18/38 ,  C08G18/75 ,  C08G18/78 ,  C08L33/06 ,  C08L75/04

    Abstract: The invention relates to amphiphilic polymer compositions, to a method for their production and to their use for producing aqueous active ingredient compositions of water-insoluble active ingredients, in particular active ingredients for crop protection. The amphiphilic polymer compositions are obtained by reacting a) at least one hydrophobic polymer P1, which carries functional groups R1 that are reactive in relation to isocyanate groups and which is composed of ethylenically unsaturated monomers M1, comprising: a1) at least 10 wt. %, (in relation to the total quantity of the monomers M1), of monomers M1a of general formula (I), in which X represents oxygen or an N-R4 group; R1, R2, R3, and R4 are defined as cited in the claims and the description; a2) up to 90 wt. %, (in relation to the total quantity of the monomers M1) of neutral, monoethylenically unsaturated monomers M1b, whose solubility in water at 25 ~C is less than 50 g/l and which differ from the monomers M1a; and a3) up to 30 wt. %, (in relation to the total quantity of the monomers M1, of ethylenically unsaturated monomers M1c, which differ from the monomers M1a and M1b, b) at least one hydrophilic polymer P2, which carries functional groups R2 that are reactive in relation to isocyanate groups, c) with at least one compound V, which has a functionality of at least 1.5 in relation to the isocyanate groups.

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