SE358631
1,240,254. Pentaerythritol. KOEI CHEMTCAL CO. Ltd. 24 Feb., 1969 [2 March, 1968], No. 9854/69. Heading C2C. A process for the continuous production of pentaerythritol comprises arranging a series of two or more upright cylindrical reactors connected successively; each reactor consisting of a mixing...
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description | 1,240,254. Pentaerythritol. KOEI CHEMTCAL CO. Ltd. 24 Feb., 1969 [2 March, 1968], No. 9854/69. Heading C2C. A process for the continuous production of pentaerythritol comprises arranging a series of two or more upright cylindrical reactors connected successively; each reactor consisting of a mixing part, a cooling part and a reaction part, continuously feeding a mixture of formaldehyde and an alkaline condensing agent to the mixing part of the first reactor and passing-the reaction mixture through the series of reactors successively, while continuously feeding acetaldehyde to the mixing part of each reactor, the residenc e time of the reaction mixture in the mixing par t being less than one minute, the ratio of the height to. diameter of the reaction part being 7 or more, (thus giving plug flow) the residence time of the reaction mixture in each reactor being 5 to 30 minutes and optionally more than 30 minutes up to 1 hour in the final reactor, the linear velocity in the reaction part being higher than 0À2 m./min., the reaction product solution coming out of the final reactor being neutralized with formic or sulphuric acid, and the neutralized solution being concentrated under normal or superatmospheric pressure in a first stage and then under reduced pressure in a second stage. Each reactor may consist of a mixing part, a cooling part and a reaction part integrally arranged successively in the upward direction, or cooling means may be provided in the mixing part. The vapour of ECHO and H 2 0 from the top of the distillation tower in the first stage may be used as a steam source for the second concentration stage- and then recycled to the first reactor. |
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A process for the continuous production of pentaerythritol comprises arranging a series of two or more upright cylindrical reactors connected successively; each reactor consisting of a mixing part, a cooling part and a reaction part, continuously feeding a mixture of formaldehyde and an alkaline condensing agent to the mixing part of the first reactor and passing-the reaction mixture through the series of reactors successively, while continuously feeding acetaldehyde to the mixing part of each reactor, the residenc e time of the reaction mixture in the mixing par t being less than one minute, the ratio of the height to. diameter of the reaction part being 7 or more, (thus giving plug flow) the residence time of the reaction mixture in each reactor being 5 to 30 minutes and optionally more than 30 minutes up to 1 hour in the final reactor, the linear velocity in the reaction part being higher than 0À2 m./min., the reaction product solution coming out of the final reactor being neutralized with formic or sulphuric acid, and the neutralized solution being concentrated under normal or superatmospheric pressure in a first stage and then under reduced pressure in a second stage. Each reactor may consist of a mixing part, a cooling part and a reaction part integrally arranged successively in the upward direction, or cooling means may be provided in the mixing part. The vapour of ECHO and H 2 0 from the top of the distillation tower in the first stage may be used as a steam source for the second concentration stage- and then recycled to the first reactor.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1973</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=19730806&DB=EPODOC&CC=SE&NR=358631B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19730806&DB=EPODOC&CC=SE&NR=358631B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MINATO Y,JA</creatorcontrib><creatorcontrib>YASUDA S,JA</creatorcontrib><title>SE358631</title><description>1,240,254. Pentaerythritol. KOEI CHEMTCAL CO. Ltd. 24 Feb., 1969 [2 March, 1968], No. 9854/69. Heading C2C. A process for the continuous production of pentaerythritol comprises arranging a series of two or more upright cylindrical reactors connected successively; each reactor consisting of a mixing part, a cooling part and a reaction part, continuously feeding a mixture of formaldehyde and an alkaline condensing agent to the mixing part of the first reactor and passing-the reaction mixture through the series of reactors successively, while continuously feeding acetaldehyde to the mixing part of each reactor, the residenc e time of the reaction mixture in the mixing par t being less than one minute, the ratio of the height to. diameter of the reaction part being 7 or more, (thus giving plug flow) the residence time of the reaction mixture in each reactor being 5 to 30 minutes and optionally more than 30 minutes up to 1 hour in the final reactor, the linear velocity in the reaction part being higher than 0À2 m./min., the reaction product solution coming out of the final reactor being neutralized with formic or sulphuric acid, and the neutralized solution being concentrated under normal or superatmospheric pressure in a first stage and then under reduced pressure in a second stage. Each reactor may consist of a mixing part, a cooling part and a reaction part integrally arranged successively in the upward direction, or cooling means may be provided in the mixing part. The vapour of ECHO and H 2 0 from the top of the distillation tower in the first stage may be used as a steam source for the second concentration stage- and then recycled to the first reactor.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1973</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZOAIdjU2tTAzNuRhYE1LzClO5YXS3Axybq4hzh66qQX58anFBYnJqXmpJfEw5U7GBBUAAGCGGZ8</recordid><startdate>19730806</startdate><enddate>19730806</enddate><creator>MINATO Y,JA</creator><creator>YASUDA S,JA</creator><scope>EVB</scope></search><sort><creationdate>19730806</creationdate><title>SE358631</title><author>MINATO Y,JA ; YASUDA S,JA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_SE358631B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1973</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>MINATO Y,JA</creatorcontrib><creatorcontrib>YASUDA S,JA</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MINATO Y,JA</au><au>YASUDA S,JA</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SE358631</title><date>1973-08-06</date><risdate>1973</risdate><abstract>1,240,254. Pentaerythritol. KOEI CHEMTCAL CO. Ltd. 24 Feb., 1969 [2 March, 1968], No. 9854/69. Heading C2C. A process for the continuous production of pentaerythritol comprises arranging a series of two or more upright cylindrical reactors connected successively; each reactor consisting of a mixing part, a cooling part and a reaction part, continuously feeding a mixture of formaldehyde and an alkaline condensing agent to the mixing part of the first reactor and passing-the reaction mixture through the series of reactors successively, while continuously feeding acetaldehyde to the mixing part of each reactor, the residenc e time of the reaction mixture in the mixing par t being less than one minute, the ratio of the height to. diameter of the reaction part being 7 or more, (thus giving plug flow) the residence time of the reaction mixture in each reactor being 5 to 30 minutes and optionally more than 30 minutes up to 1 hour in the final reactor, the linear velocity in the reaction part being higher than 0À2 m./min., the reaction product solution coming out of the final reactor being neutralized with formic or sulphuric acid, and the neutralized solution being concentrated under normal or superatmospheric pressure in a first stage and then under reduced pressure in a second stage. Each reactor may consist of a mixing part, a cooling part and a reaction part integrally arranged successively in the upward direction, or cooling means may be provided in the mixing part. The vapour of ECHO and H 2 0 from the top of the distillation tower in the first stage may be used as a steam source for the second concentration stage- and then recycled to the first reactor.</abstract><oa>free_for_read</oa></addata></record> |
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title | SE358631 |
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