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11.
公开(公告)号:BRPI0918489A2
公开(公告)日:2015-12-01
申请号:BRPI0918489
申请日:2009-09-07
Applicant: BASF SE
Inventor: HENKELMANN JOCHEM , EMMELUTH MARIO , MACHHAMMER OTTO , GIESA SONJA , ROHDE WOLFGANG
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公开(公告)号:PT2084128E
公开(公告)日:2014-06-12
申请号:PT07821518
申请日:2007-10-18
Applicant: BASF SE
Inventor: STROEFER ECKHARD , MAIXNER STEFAN , HENKELMANN JOCHEM , BÖHLING RALF , KÜBER SVEN , KRUG GEORG , BOLZ WERNER
IPC: C07C263/10 , B01J19/00
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13.
公开(公告)号:DE502007005974D1
公开(公告)日:2011-01-27
申请号:DE502007005974
申请日:2007-07-25
Applicant: BASF SE
Inventor: HENKELMANN JOCHEM , BECKER MICHAEL , RICHTER FELIX , SCHAEFER THOMAS
IPC: B01J23/46 , B01J38/04 , C07C51/36 , C07C67/303
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公开(公告)号:ES2476248T3
公开(公告)日:2014-07-14
申请号:ES07821518
申请日:2007-10-18
Applicant: BASF SE
Inventor: BÖHLING RALF , KÜBER SVEN , MAIXNER STEFAN , STROEFER ECKHARD , HENKELMANN JOCHEM , KRUG GEORG , BOLZ WERNER
IPC: C07C263/10 , B01J19/00
Abstract: Un procedimiento para la preparación de isocianatos por fosgenación de aminas, caracterizado porque fosgeno y amina se ponen en contacto en al menos 2 cámaras de mezcla conectadas en paralelo, utilizándose como cámaras de mezcla cámaras de mezcla microestructuradasde mezcla.
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公开(公告)号:DK2097366T3
公开(公告)日:2011-02-21
申请号:DK00993318
申请日:2000-11-27
Applicant: BASF SE
Inventor: STAMM ARMIN , GOETZ ROLAND , GOETZ NORBERT , HENKELMANN JOCHEM , KNEUPER HEINZ-JOSEF , WOLF BERND
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公开(公告)号:AT482928T
公开(公告)日:2010-10-15
申请号:AT03763693
申请日:2003-07-03
Applicant: BASF SE
Inventor: HENKELMANN JOCHEM , WEBER THEODOR , ROHDE THORSTEN , BUSCH RALPH
IPC: C07C273/18 , C07C275/06
Abstract: The invention relates to a process for the preparation of tetrasubstituted ureas by reaction of the corresponding amines with phosgene in the presence of an aqueous inorganic base at a temperature in the range from 0 to 150° C., which comprises: feeding the corresponding amine, the phosgene and the aqueous inorganic base on average continuously to the reaction apparatus, forming a two-phase system in the reaction apparatus through the choice of the tetrasubstituted ureas to be prepared, through the mixing ratios of the substances and substance mixtures to be fed in, through the temperature during the reaction and, where appropriate, through the feed of an organic solvent which is not completely miscible with water, and discharging the reaction mixture on average continuously from the reaction apparatus.
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公开(公告)号:UA89906C2
公开(公告)日:2010-03-10
申请号:UAA200811765
申请日:2007-03-02
Applicant: BASF SE
Inventor: HENKELMANN JOCHEM , BECKER MICHAEL , BUERKLE JOCHEN , WAHL PETER , THEIS GERHARD , MAURER STEPHAN
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公开(公告)号:DE502005004314D1
公开(公告)日:2008-07-10
申请号:DE502005004314
申请日:2005-11-24
Applicant: BASF SE
Inventor: ROHDE THORSTEN , HENKELMANN JOCHEM
Abstract: A process for preparing phthaloyl chloride by reacting phthalic anhydride with a chlorinating agent (I) selected from the group of thionyl chloride and phosgene in the presence of a catalyst at a temperature of from 80 to 200° C. and a pressure of from 0.01 to 10 MPa abs, in which the catalyst (II) used is triphenylphosphine, triphenylphosphine oxide or a mixture thereof.
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公开(公告)号:DE502005004057D1
公开(公告)日:2008-06-19
申请号:DE502005004057
申请日:2005-12-14
Applicant: BASF SE
Inventor: OSSWALD FRIEDERIKE , BRAUCH KARL HEINZ , BOETTCHER ARND , HENKELMANN JOCHEM , VAN LAAR FREDERIK , GERLACH TILL
IPC: C07C209/72
Abstract: A process for preparing 1,2-diamino-3-methylcyclohexane and/or 1,2-diamino-4-methylcyclohexane by reacting 2,3- and/or 3,4-diaminotoluene with hydrogen at elevated pressure and elevated temperature in the presence of a heterogeneous rhodium catalyst, wherein a mixture comprising 2,3- and/or 3,4-diaminotoluene, a dialkyl ether and/or alicyclic ether as a solvent and ammonia is initially charged in an autoclave in the presence of the catalyst and subsequently hydrogenated while supplying hydrogen.
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公开(公告)号:ES2295855T3
公开(公告)日:2008-04-16
申请号:ES04727886
申请日:2004-04-16
Applicant: BASF SE
Inventor: KLASS KATRIN , BECKER HEIKE , VOGELSANG REGINA , HAUK ALEXANDER , SIEGERT MARKUS , HENKELMANN JOCHEM
Abstract: Procedimiento para la elaboración continua de metilviniléter mediante reacción de metanol con etino en la fase líquida en presencia de un compuesto metálico alcalino o alcalino térreo básico a una temperatura de 40 a 300°C y una presión de 0, 1 a 5MPaabs, caracterizado porque la reacción se efectúa en ausencia de una fase gaseosa continua y a una concentración de metilviniléter en toda la fase líquida = 30% en peso.
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