Removal of bromobutanone from acetic acid

Acetic acid can be prepared in high conversions and selectively by the oxidation of liquid n-butane at temperatures of from 120 DEG C. up to 230 DEG C. in the presence of an acetic acid solution containing bromine ions in combination with ions of cobalt or cobalt and manganese. The debutanized efflu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: HARPER, JON J, ZEITLIN, MARTIN A
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator HARPER
JON J
ZEITLIN
MARTIN A
description Acetic acid can be prepared in high conversions and selectively by the oxidation of liquid n-butane at temperatures of from 120 DEG C. up to 230 DEG C. in the presence of an acetic acid solution containing bromine ions in combination with ions of cobalt or cobalt and manganese. The debutanized effluent of such oxidation consists mainly of acetic acid and water but also contains esters and ketones boiling lower than acetic acid, some higher carbon content aliphatic acids and metal salts boiling higher than acetic acid and rather small amounts of 3-bromo-2-butanone which, although boiling higher than acetic acid, cannot be separated by simple distillation as can be the other non-acetic acid organic impurities. The present inventive technique for removal of said bromo-ketone has for its concept the use of a combination of cryogenic crystallization and removal of adhering mother liquor which can be practiced continuously in known apparatus devised for other fractional crystallizations.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_US4338464A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>US4338464A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_US4338464A3</originalsourceid><addsrcrecordid>eNrjZNAMSs3NL0vMUchPU0gqys_NTyotSczLz0tVSAPyFBKTU0syk4FUZgoPA2taYk5xKi-U5maQd3MNcfbQTS3Ij08tLgAqzUstiQ8NNjE2tjAxM3E0JqwCAF--J-4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Removal of bromobutanone from acetic acid</title><source>esp@cenet</source><creator>HARPER; JON J ; ZEITLIN; MARTIN A</creator><creatorcontrib>HARPER; JON J ; ZEITLIN; MARTIN A</creatorcontrib><description>Acetic acid can be prepared in high conversions and selectively by the oxidation of liquid n-butane at temperatures of from 120 DEG C. up to 230 DEG C. in the presence of an acetic acid solution containing bromine ions in combination with ions of cobalt or cobalt and manganese. The debutanized effluent of such oxidation consists mainly of acetic acid and water but also contains esters and ketones boiling lower than acetic acid, some higher carbon content aliphatic acids and metal salts boiling higher than acetic acid and rather small amounts of 3-bromo-2-butanone which, although boiling higher than acetic acid, cannot be separated by simple distillation as can be the other non-acetic acid organic impurities. The present inventive technique for removal of said bromo-ketone has for its concept the use of a combination of cryogenic crystallization and removal of adhering mother liquor which can be practiced continuously in known apparatus devised for other fractional crystallizations.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1982</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&amp;date=19820706&amp;DB=EPODOC&amp;CC=US&amp;NR=4338464A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19820706&amp;DB=EPODOC&amp;CC=US&amp;NR=4338464A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HARPER; JON J</creatorcontrib><creatorcontrib>ZEITLIN; MARTIN A</creatorcontrib><title>Removal of bromobutanone from acetic acid</title><description>Acetic acid can be prepared in high conversions and selectively by the oxidation of liquid n-butane at temperatures of from 120 DEG C. up to 230 DEG C. in the presence of an acetic acid solution containing bromine ions in combination with ions of cobalt or cobalt and manganese. The debutanized effluent of such oxidation consists mainly of acetic acid and water but also contains esters and ketones boiling lower than acetic acid, some higher carbon content aliphatic acids and metal salts boiling higher than acetic acid and rather small amounts of 3-bromo-2-butanone which, although boiling higher than acetic acid, cannot be separated by simple distillation as can be the other non-acetic acid organic impurities. The present inventive technique for removal of said bromo-ketone has for its concept the use of a combination of cryogenic crystallization and removal of adhering mother liquor which can be practiced continuously in known apparatus devised for other fractional crystallizations.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1982</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNAMSs3NL0vMUchPU0gqys_NTyotSczLz0tVSAPyFBKTU0syk4FUZgoPA2taYk5xKi-U5maQd3MNcfbQTS3Ij08tLgAqzUstiQ8NNjE2tjAxM3E0JqwCAF--J-4</recordid><startdate>19820706</startdate><enddate>19820706</enddate><creator>HARPER; JON J</creator><creator>ZEITLIN; MARTIN A</creator><scope>EVB</scope></search><sort><creationdate>19820706</creationdate><title>Removal of bromobutanone from acetic acid</title><author>HARPER; JON J ; ZEITLIN; MARTIN A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US4338464A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1982</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>HARPER; JON J</creatorcontrib><creatorcontrib>ZEITLIN; MARTIN A</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HARPER; JON J</au><au>ZEITLIN; MARTIN A</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Removal of bromobutanone from acetic acid</title><date>1982-07-06</date><risdate>1982</risdate><abstract>Acetic acid can be prepared in high conversions and selectively by the oxidation of liquid n-butane at temperatures of from 120 DEG C. up to 230 DEG C. in the presence of an acetic acid solution containing bromine ions in combination with ions of cobalt or cobalt and manganese. The debutanized effluent of such oxidation consists mainly of acetic acid and water but also contains esters and ketones boiling lower than acetic acid, some higher carbon content aliphatic acids and metal salts boiling higher than acetic acid and rather small amounts of 3-bromo-2-butanone which, although boiling higher than acetic acid, cannot be separated by simple distillation as can be the other non-acetic acid organic impurities. The present inventive technique for removal of said bromo-ketone has for its concept the use of a combination of cryogenic crystallization and removal of adhering mother liquor which can be practiced continuously in known apparatus devised for other fractional crystallizations.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_US4338464A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
title Removal of bromobutanone from acetic acid
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T01%3A55%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=HARPER;%20JON%20J&rft.date=1982-07-06&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EUS4338464A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true