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公开(公告)号:MY136695A
公开(公告)日:2008-11-28
申请号:MYPI20045180
申请日:2004-12-16
Applicant: BASF AG
Inventor: STEINBRENNER ULRICH DR , HEIDEMANN THOMAS DR , ROEPER MICHAEL PROF DR , STEPHAN JUERGEN DR , NARBESHUBER THOMAS DR , TROPSCH JURGEN DR , BOTTKE NILS DR , BENFER REGINA DR
IPC: C07C2/66 , C07C303/06 , C07C309/31 , C11D1/22 , C11D11/04
Abstract: The preparation of alkylaryl compounds takes place by a) reaction of a C 4 /C 5 -olefin mixture over a metathesis catalyst to prepare a C 4-8 -olefin mixture comprising 2-pentene, and optional removal of the C 4-8 -olefin mixture, b) removal of from 5 to 100% of the 2-pentene present in stage a) and subsequent reaction over an isomerization catalyst to give a mixture of 2-pentene and 1-pentene which is returned to stage a), c) dimerization of the C 4-8 -olefin mixture obtained in stage b) following removal in the presence of a dimerization catalyst to give a mixture containing C 8-16 -olefins, removal of these C 8-16 -olefins and optional removal of a partial stream thereof, d) reaction of the c 8-16 -olefin mixtures obtained in stage c) or of the partial stream with an aromatic hydrocarbon in the presence of an alkylation catalyst to form alkyl aromatic compounds where, prior to the reaction, 0 to 60% by weight, based on the c 8-16 -olefin mixtures obtained in stage c), of linear olefins may additionally be added, e) optional sulfonation of the alkyl aromatic compounds obtained in stage d) and neutralization to give alkylarylsulfonates, where, prior to the sulfonation, 0 to 60% by weight, based on the alkyl aromatic compounds obtained in stage d), of linear alkylbenzenes may additionally be added if no admixing has taken place in stage d), f) optional mixing of the alkylarylsulfonates obtained in stage e) with 0 to 60% by weight, based on the alkylarylsulfonates obtained in stage e), of linear alkylarylsulfonate, if no admixing has taken place in stages d) and e).
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公开(公告)号:MY140598A
公开(公告)日:2009-12-31
申请号:MYPI20044406
申请日:2004-10-26
Applicant: BASF AG
Inventor: BOTTKE NILS DR , BENFER REGINA DR , BOSCH MARCO DR , NARBESHUBER THOMAS DR , STEINBRENNER ULRICH DR , STEPHAN JUERGEN DR
Abstract: IN A PROCESS FOR PREPARING ALKYLARYL COMPOUNDS BY REACTING A C10-14-MONOOLEFIN MIXTURE WITH AN AROMATIC HYDROCARBON IN THE PRESENCE OF AN ALKYLATION CATALYST TO FORM ALKYL AROMATIC COMPOUNDS AND IF APPROPRIATE SUBSEQUENTLY SULFONATING AND NEUTRALIZING THE RESULTING ALKYLARYL COMPOUNDS, IN THE C10-14-MONOOLEFINS, ON AVERAGE, MORE THAN 0AND UP TO 100OF METHYL BRANCHES ARE PRESENT IN THE LONGEST CARBON CHAIN AND FEWER THAN 50OF THE METHYL BRANCHES ARE IN THE 2-, 3- AND 4-POSITION, CALCULATED STARTING FROM THE CHAIN ENDS OF THE LONGEST CARBON CHAIN.
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公开(公告)号:MY139380A
公开(公告)日:2009-09-30
申请号:MYPI20023670
申请日:2002-10-01
Applicant: BASF AG
Inventor: STEINBRENNER ULRICH DR , HEIDEMANN THOMAS DR , SCHINDLER GOETZ-PETER DR , STEPHAN JUERGEN DR , MAAS HEIKO DR
IPC: C07C15/00 , C07C309/31 , C11D1/22
Abstract: THE PREPARATION OF ALKYLARYL COMPOUNDS TAKES PLACE, INTER ALIA, BYA1) PREPARATION OF C4-OLEFIN MIXTURE FROM LPG, LNG OR MTO STREAMS,@B1) REACTION OF THE C4-OLEFIN MIXTURE OBTAINED IN THIS WAY OVER A METATHESIS CATALYST FOR THE PREPARATION OF AN OLEFIN MIXTURE COMPRISING 2-PENTENE AND/ OR 3-HEXENE AND OPTIONAL REMOVAL OF 2-PENTENE AND/ OR 3-HEXENE,CI) DIMERIZATION OF THE 2-PENTENE AND/OR 3-HEXENE OBTAINED IN STAGE B1) OVER A DIMERIZATION CATALYST TO GIVE A MIXTURE COMPRISNG C10-12 OLEFINS,D1) REACTION OF THE C10-12 OLEFIN MIXTURE OBTAINED IN STAGE B1) WITH AN AROMATIC HYDROCARBON IN THE PRESENCE OF AN ALKYLATION CATALYST TO FORM ALKYLAROMATIC COMPOUNDS, IT BEING POSSIBLE TO ADD ADDITIONAL LINEAR OLEFINS PRIOR TO THE REACTION.
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