VERFAHREN ZUR GLEICHZEITIGEN HERSTELLUNG VON REINEM MTB UND WEITGEHEND ISOBUTENFREIEM C TIEF 4 -KOHLENWASSERSTOFFGEMISCH
A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C4-hydrocarbons, by reacting the isobutene contained in the mixture of C4-hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly aci...
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creator | OBENAUS,FRITZ,DR DROSTE,WILHELM,DR |
description | A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C4-hydrocarbons, by reacting the isobutene contained in the mixture of C4-hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins. The process has the following steps: (a) methanol and isobutene are reacted in a molar ratio of 2:1 to 5:1 at temperatures between 30 DEG and 100 DEG C.; (b) the unconverted hydrocarbons are then removed as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) the bottom product from this first column is rectified in a second column under normal pressure or under a slight excess pressure of up to 2 bars at the top of the column, the bottom product of this rectification is recycled to reaction zone (a), if necessary, after separating off a portion of the tertiary butanol formed and the C8-olefins; and (d) the distillate from this second column is rectified in a third rectification column under a pressure of 5 to 30 bars, the distillate thus obtained is recycled into the feed to the second column and pure methyl tertiary butyl ether is withdrawn from the bottom of the third column. |
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The process has the following steps: (a) methanol and isobutene are reacted in a molar ratio of 2:1 to 5:1 at temperatures between 30 DEG and 100 DEG C.; (b) the unconverted hydrocarbons are then removed as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) the bottom product from this first column is rectified in a second column under normal pressure or under a slight excess pressure of up to 2 bars at the top of the column, the bottom product of this rectification is recycled to reaction zone (a), if necessary, after separating off a portion of the tertiary butanol formed and the C8-olefins; and (d) the distillate from this second column is rectified in a third rectification column under a pressure of 5 to 30 bars, the distillate thus obtained is recycled into the feed to the second column and pure methyl tertiary butyl ether is withdrawn from the bottom of the third column.</description><edition>3</edition><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; APPARATUS THEREFOR ; CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY ; CHEMISTRY ; GENERAL METHODS OF ORGANIC CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY ; PERFORMING OPERATIONS ; PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL ; THEIR RELEVANT APPARATUS ; TRANSPORTING</subject><creationdate>1980</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19800619&DB=EPODOC&CC=DE&NR=2853769A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25544,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19800619&DB=EPODOC&CC=DE&NR=2853769A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>OBENAUS,FRITZ,DR</creatorcontrib><creatorcontrib>DROSTE,WILHELM,DR</creatorcontrib><title>VERFAHREN ZUR GLEICHZEITIGEN HERSTELLUNG VON REINEM MTB UND WEITGEHEND ISOBUTENFREIEM C TIEF 4 -KOHLENWASSERSTOFFGEMISCH</title><description>A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C4-hydrocarbons, by reacting the isobutene contained in the mixture of C4-hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins. The process has the following steps: (a) methanol and isobutene are reacted in a molar ratio of 2:1 to 5:1 at temperatures between 30 DEG and 100 DEG C.; (b) the unconverted hydrocarbons are then removed as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) the bottom product from this first column is rectified in a second column under normal pressure or under a slight excess pressure of up to 2 bars at the top of the column, the bottom product of this rectification is recycled to reaction zone (a), if necessary, after separating off a portion of the tertiary butanol formed and the C8-olefins; and (d) the distillate from this second column is rectified in a third rectification column under a pressure of 5 to 30 bars, the distillate thus obtained is recycled into the feed to the second column and pure methyl tertiary butyl ether is withdrawn from the bottom of the third column.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>APPARATUS THEREFOR</subject><subject>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>GENERAL METHODS OF ORGANIC CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PERFORMING OPERATIONS</subject><subject>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</subject><subject>THEIR RELEVANT APPARATUS</subject><subject>TRANSPORTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1980</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNzEsKwjAYBOBuXIh6h_8CXWh9LvuYPDBNIElb6KYUiSvRgi48vhE8gKsZho-ZJ-8WluXCQlPfWOIKshQ9pJc8TgLWeSjVaE6t0WQhNWqqfUGNrqiLjkMgVulM0XhoFkkUJXkJRltKz0Yo6C537vtlGOOopSvFMpldx9szrH65SIjBlyIN02MIz2m8hHt4DRU2x1122J_ydfYH-QBnajn_</recordid><startdate>19800619</startdate><enddate>19800619</enddate><creator>OBENAUS,FRITZ,DR</creator><creator>DROSTE,WILHELM,DR</creator><scope>EVB</scope></search><sort><creationdate>19800619</creationdate><title>VERFAHREN ZUR GLEICHZEITIGEN HERSTELLUNG VON REINEM MTB UND WEITGEHEND ISOBUTENFREIEM C TIEF 4 -KOHLENWASSERSTOFFGEMISCH</title><author>OBENAUS,FRITZ,DR ; DROSTE,WILHELM,DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE2853769A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1980</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>APPARATUS THEREFOR</topic><topic>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>GENERAL METHODS OF ORGANIC CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PERFORMING OPERATIONS</topic><topic>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</topic><topic>THEIR RELEVANT APPARATUS</topic><topic>TRANSPORTING</topic><toplevel>online_resources</toplevel><creatorcontrib>OBENAUS,FRITZ,DR</creatorcontrib><creatorcontrib>DROSTE,WILHELM,DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>OBENAUS,FRITZ,DR</au><au>DROSTE,WILHELM,DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>VERFAHREN ZUR GLEICHZEITIGEN HERSTELLUNG VON REINEM MTB UND WEITGEHEND ISOBUTENFREIEM C TIEF 4 -KOHLENWASSERSTOFFGEMISCH</title><date>1980-06-19</date><risdate>1980</risdate><abstract>A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C4-hydrocarbons, by reacting the isobutene contained in the mixture of C4-hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins. The process has the following steps: (a) methanol and isobutene are reacted in a molar ratio of 2:1 to 5:1 at temperatures between 30 DEG and 100 DEG C.; (b) the unconverted hydrocarbons are then removed as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) the bottom product from this first column is rectified in a second column under normal pressure or under a slight excess pressure of up to 2 bars at the top of the column, the bottom product of this rectification is recycled to reaction zone (a), if necessary, after separating off a portion of the tertiary butanol formed and the C8-olefins; and (d) the distillate from this second column is rectified in a third rectification column under a pressure of 5 to 30 bars, the distillate thus obtained is recycled into the feed to the second column and pure methyl tertiary butyl ether is withdrawn from the bottom of the third column.</abstract><edition>3</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS APPARATUS THEREFOR CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY CHEMISTRY GENERAL METHODS OF ORGANIC CHEMISTRY METALLURGY ORGANIC CHEMISTRY PERFORMING OPERATIONS PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL THEIR RELEVANT APPARATUS TRANSPORTING |
title | VERFAHREN ZUR GLEICHZEITIGEN HERSTELLUNG VON REINEM MTB UND WEITGEHEND ISOBUTENFREIEM C TIEF 4 -KOHLENWASSERSTOFFGEMISCH |
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