Loading…
Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids
Oxidation of aqueous solutions of 3-hydroxypropionic (3-HPA) and propionic acids (PA) was studied in a titanium high-pressure reactor at 280−310 °C using oxygen partial pressures between 10 and 45 bar. Oxidation of both acids was found to obey first-order kinetic with respect to their concentrations...
Saved in:
Published in: | Industrial & engineering chemistry research 1999-07, Vol.38 (7), p.2557-2563 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63 |
---|---|
cites | cdi_FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63 |
container_end_page | 2563 |
container_issue | 7 |
container_start_page | 2557 |
container_title | Industrial & engineering chemistry research |
container_volume | 38 |
creator | Shende, Rajesh V Levec, Janez |
description | Oxidation of aqueous solutions of 3-hydroxypropionic (3-HPA) and propionic acids (PA) was studied in a titanium high-pressure reactor at 280−310 °C using oxygen partial pressures between 10 and 45 bar. Oxidation of both acids was found to obey first-order kinetic with respect to their concentrations as well as to their lumped TOC concentrations. Oxidation rate revealed a half order dependence with respect to oxygen for oxidation of both acids. In the case of 3-HPA oxidation, the activation energy was found to be 135 kJ/mol, and it was 140 kJ/mol when lumped concentration TOC was used. The activation energy for PA oxidation is 150 kJ/mol, and it is slightly higher, 158 kJ/mol, for TOC reduction. Almost complete conversion of 3-HPA was achieved at 300 °C after 1 h, whereas 95% conversion of PA acid was obtained at 310 °C after 3 h. During oxidation of 3-HPA, 3-oxopropionic and acetic acids were identified as intermediate products. Oxidation of PA yielded acetic and formic acids as intermediates; at oxygen partial pressures above 25 bar and 310 °C, the formation of acetic acid was appreciably reduced. In both cases, however, direct oxidation to carbon dioxide and water was found to be the main reaction route. |
doi_str_mv | 10.1021/ie9900061 |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ie9900061</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a794705273</sourcerecordid><originalsourceid>FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63</originalsourceid><addsrcrecordid>eNptjz1PwzAQhi0EEqUw8A8ywMAQsB1f7Iyl0BZRqZUodLQcf0guJYnsILX_nlRBZWG603vP3elB6Jrge4IpefC2KDDGOTlBAwIUp4AZnKIBFkKkIASco4sYNx0CwNgAjV99ZVuvY1K7ZG3bZLHzRrW-rg7BMtRN13qdqMokWTrbm1Dv9s0xHmlv4iU6c2ob7dVvHaL3yfNqPEvni-nLeDRPVSZ4m1Jn8oLY3BrDwApFCqoYzwpnMTcUjLY4w4K6stSdCrXAFAatCC2pNq7MsyG66-_qUMcYrJNN8F8q7CXB8mAvj_Yde9OzjYpabV1Qlfbxb0EAZAXvsLTHfGzt7jhW4VPmPOMgV8s3-TSFNeOPE_nR8bc9r3SUm_o7VJ3wP-9_AIgMc_c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Shende, Rajesh V ; Levec, Janez</creator><creatorcontrib>Shende, Rajesh V ; Levec, Janez</creatorcontrib><description>Oxidation of aqueous solutions of 3-hydroxypropionic (3-HPA) and propionic acids (PA) was studied in a titanium high-pressure reactor at 280−310 °C using oxygen partial pressures between 10 and 45 bar. Oxidation of both acids was found to obey first-order kinetic with respect to their concentrations as well as to their lumped TOC concentrations. Oxidation rate revealed a half order dependence with respect to oxygen for oxidation of both acids. In the case of 3-HPA oxidation, the activation energy was found to be 135 kJ/mol, and it was 140 kJ/mol when lumped concentration TOC was used. The activation energy for PA oxidation is 150 kJ/mol, and it is slightly higher, 158 kJ/mol, for TOC reduction. Almost complete conversion of 3-HPA was achieved at 300 °C after 1 h, whereas 95% conversion of PA acid was obtained at 310 °C after 3 h. During oxidation of 3-HPA, 3-oxopropionic and acetic acids were identified as intermediate products. Oxidation of PA yielded acetic and formic acids as intermediates; at oxygen partial pressures above 25 bar and 310 °C, the formation of acetic acid was appreciably reduced. In both cases, however, direct oxidation to carbon dioxide and water was found to be the main reaction route.</description><identifier>ISSN: 0888-5885</identifier><identifier>EISSN: 1520-5045</identifier><identifier>DOI: 10.1021/ie9900061</identifier><identifier>CODEN: IECRED</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Chemistry ; Exact sciences and technology ; Industrial wastewaters ; Kinetics and mechanisms ; Organic chemistry ; Pollution ; Reactivity and mechanisms ; Wastewaters ; Water treatment and pollution</subject><ispartof>Industrial & engineering chemistry research, 1999-07, Vol.38 (7), p.2557-2563</ispartof><rights>Copyright © 1999 American Chemical Society</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63</citedby><cites>FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1855397$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Shende, Rajesh V</creatorcontrib><creatorcontrib>Levec, Janez</creatorcontrib><title>Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids</title><title>Industrial & engineering chemistry research</title><addtitle>Ind. Eng. Chem. Res</addtitle><description>Oxidation of aqueous solutions of 3-hydroxypropionic (3-HPA) and propionic acids (PA) was studied in a titanium high-pressure reactor at 280−310 °C using oxygen partial pressures between 10 and 45 bar. Oxidation of both acids was found to obey first-order kinetic with respect to their concentrations as well as to their lumped TOC concentrations. Oxidation rate revealed a half order dependence with respect to oxygen for oxidation of both acids. In the case of 3-HPA oxidation, the activation energy was found to be 135 kJ/mol, and it was 140 kJ/mol when lumped concentration TOC was used. The activation energy for PA oxidation is 150 kJ/mol, and it is slightly higher, 158 kJ/mol, for TOC reduction. Almost complete conversion of 3-HPA was achieved at 300 °C after 1 h, whereas 95% conversion of PA acid was obtained at 310 °C after 3 h. During oxidation of 3-HPA, 3-oxopropionic and acetic acids were identified as intermediate products. Oxidation of PA yielded acetic and formic acids as intermediates; at oxygen partial pressures above 25 bar and 310 °C, the formation of acetic acid was appreciably reduced. In both cases, however, direct oxidation to carbon dioxide and water was found to be the main reaction route.</description><subject>Applied sciences</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Industrial wastewaters</subject><subject>Kinetics and mechanisms</subject><subject>Organic chemistry</subject><subject>Pollution</subject><subject>Reactivity and mechanisms</subject><subject>Wastewaters</subject><subject>Water treatment and pollution</subject><issn>0888-5885</issn><issn>1520-5045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNptjz1PwzAQhi0EEqUw8A8ywMAQsB1f7Iyl0BZRqZUodLQcf0guJYnsILX_nlRBZWG603vP3elB6Jrge4IpefC2KDDGOTlBAwIUp4AZnKIBFkKkIASco4sYNx0CwNgAjV99ZVuvY1K7ZG3bZLHzRrW-rg7BMtRN13qdqMokWTrbm1Dv9s0xHmlv4iU6c2ob7dVvHaL3yfNqPEvni-nLeDRPVSZ4m1Jn8oLY3BrDwApFCqoYzwpnMTcUjLY4w4K6stSdCrXAFAatCC2pNq7MsyG66-_qUMcYrJNN8F8q7CXB8mAvj_Yde9OzjYpabV1Qlfbxb0EAZAXvsLTHfGzt7jhW4VPmPOMgV8s3-TSFNeOPE_nR8bc9r3SUm_o7VJ3wP-9_AIgMc_c</recordid><startdate>19990701</startdate><enddate>19990701</enddate><creator>Shende, Rajesh V</creator><creator>Levec, Janez</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990701</creationdate><title>Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids</title><author>Shende, Rajesh V ; Levec, Janez</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Applied sciences</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Industrial wastewaters</topic><topic>Kinetics and mechanisms</topic><topic>Organic chemistry</topic><topic>Pollution</topic><topic>Reactivity and mechanisms</topic><topic>Wastewaters</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shende, Rajesh V</creatorcontrib><creatorcontrib>Levec, Janez</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Industrial & engineering chemistry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shende, Rajesh V</au><au>Levec, Janez</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids</atitle><jtitle>Industrial & engineering chemistry research</jtitle><addtitle>Ind. Eng. Chem. Res</addtitle><date>1999-07-01</date><risdate>1999</risdate><volume>38</volume><issue>7</issue><spage>2557</spage><epage>2563</epage><pages>2557-2563</pages><issn>0888-5885</issn><eissn>1520-5045</eissn><coden>IECRED</coden><abstract>Oxidation of aqueous solutions of 3-hydroxypropionic (3-HPA) and propionic acids (PA) was studied in a titanium high-pressure reactor at 280−310 °C using oxygen partial pressures between 10 and 45 bar. Oxidation of both acids was found to obey first-order kinetic with respect to their concentrations as well as to their lumped TOC concentrations. Oxidation rate revealed a half order dependence with respect to oxygen for oxidation of both acids. In the case of 3-HPA oxidation, the activation energy was found to be 135 kJ/mol, and it was 140 kJ/mol when lumped concentration TOC was used. The activation energy for PA oxidation is 150 kJ/mol, and it is slightly higher, 158 kJ/mol, for TOC reduction. Almost complete conversion of 3-HPA was achieved at 300 °C after 1 h, whereas 95% conversion of PA acid was obtained at 310 °C after 3 h. During oxidation of 3-HPA, 3-oxopropionic and acetic acids were identified as intermediate products. Oxidation of PA yielded acetic and formic acids as intermediates; at oxygen partial pressures above 25 bar and 310 °C, the formation of acetic acid was appreciably reduced. In both cases, however, direct oxidation to carbon dioxide and water was found to be the main reaction route.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ie9900061</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0888-5885 |
ispartof | Industrial & engineering chemistry research, 1999-07, Vol.38 (7), p.2557-2563 |
issn | 0888-5885 1520-5045 |
language | eng |
recordid | cdi_crossref_primary_10_1021_ie9900061 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Applied sciences Chemistry Exact sciences and technology Industrial wastewaters Kinetics and mechanisms Organic chemistry Pollution Reactivity and mechanisms Wastewaters Water treatment and pollution |
title | Kinetics of Wet Oxidation of Propionic and 3-Hydroxypropionic Acids |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T05%3A44%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Kinetics%20of%20Wet%20Oxidation%20of%20Propionic%20and%203-Hydroxypropionic%20Acids&rft.jtitle=Industrial%20&%20engineering%20chemistry%20research&rft.au=Shende,%20Rajesh%20V&rft.date=1999-07-01&rft.volume=38&rft.issue=7&rft.spage=2557&rft.epage=2563&rft.pages=2557-2563&rft.issn=0888-5885&rft.eissn=1520-5045&rft.coden=IECRED&rft_id=info:doi/10.1021/ie9900061&rft_dat=%3Cacs_cross%3Ea794705273%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a387t-2fd691e6edd45e8a192a4739fe07d25dce03082fbbc1022e54a05ca12b2cdfb63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |