Loading…
Ignition of isomers of pentane: An experimental and kinetic modeling study
Experiments in a rapid compression machine were used to examine the influences of variations in fuel molecular structure on the autoignition of isomers of pentane. Autoignition of stoichiometric mixtures of the three isomers of pentane were studied at compressed gas initial temperatures between 640...
Saved in:
Published in: | Proceedings of the Combustion Institute 2000-01, Vol.28 (2), p.1671-1678 |
---|---|
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-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273 |
---|---|
cites | cdi_FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273 |
container_end_page | 1678 |
container_issue | 2 |
container_start_page | 1671 |
container_title | Proceedings of the Combustion Institute |
container_volume | 28 |
creator | Ribaucour, M. Minetti, R. Sochet, L.R. Curran, H.J. Pitz, W.J. Westbrook, C.K. |
description | Experiments in a rapid compression machine were used to examine the influences of variations in fuel molecular structure on the autoignition of isomers of pentane. Autoignition of stoichiometric mixtures of the three isomers of pentane were studied at compressed gas initial temperatures between 640 K and 900 K and at precompression pressures of 300 and 400 torr. Numerical simulations of the same experiments were carried out using a detailed chemical kinetic reaction mechanism. The results are interpreted in terms of a low-temperature oxidation mechanism involving addition of molecular oxygen to alkyl and hydroperoxyalkyl radicals. Results indicate that in most cases, the reactive gases experience a two-stage autoignition. The first stage follows a low-temperature alkylperoxy radical isomerization pathway that is effectively quenched when the temperature reaches a level where dissociation reactions of alkylperoxy and hydroperoxyalkylperoxy radicals are more rapid than the reverse addition steps. The second stage is controlled by the onset of dissociation of hydrogen peroxide. At the highest compression temperatures achieved, little or no first-stage ignition is observed. Particular attention is given to the influence of heat transfer and the importance of regions of variable temperature within the compressed gas volume. Implications of this work on practical ignition problems are discussed. |
doi_str_mv | 10.1016/S0082-0784(00)80566-4 |
format | article |
fullrecord | <record><control><sourceid>elsevier_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_15008099</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0082078400805664</els_id><sourcerecordid>S0082078400805664</sourcerecordid><originalsourceid>FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273</originalsourceid><addsrcrecordid>eNqFkMtOwzAQRS0EEqXwCUiW2MAiME7s2GGDqopHUSUWwNpynEkxtHYVm4r-PUnLntVczeNezSHknME1A1bevAKoPAOp-CXAlQJRlhk_ICOmZJHlEvhhrwWHTHJVHZOTGD8BCgmFGJHn2cK75IKnoaUuhhV2cZBr9Ml4vKUTT_FnjZ1bDZ0lNb6hX85jcpauQoNL5xc0pu9me0qOWrOMePZXx-T94f5t-pTNXx5n08k8s1xAyoyVVcHQ1k3e1gZLlIVsBSjJjDS85KrsZ1IYVpVK5HXLci5qLsFWtUDIZTEmF3vfEJPT0bqE9sMG79EmzUQPA6qq3xL7LduFGDts9br_wXRbzUAP2PQOmx6waQC9w6Z5f3e3v8P-hY3DbkhAb7Fx3RDQBPePwy90GnQk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Ignition of isomers of pentane: An experimental and kinetic modeling study</title><source>ScienceDirect Journals</source><creator>Ribaucour, M. ; Minetti, R. ; Sochet, L.R. ; Curran, H.J. ; Pitz, W.J. ; Westbrook, C.K.</creator><creatorcontrib>Ribaucour, M. ; Minetti, R. ; Sochet, L.R. ; Curran, H.J. ; Pitz, W.J. ; Westbrook, C.K. ; Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)</creatorcontrib><description>Experiments in a rapid compression machine were used to examine the influences of variations in fuel molecular structure on the autoignition of isomers of pentane. Autoignition of stoichiometric mixtures of the three isomers of pentane were studied at compressed gas initial temperatures between 640 K and 900 K and at precompression pressures of 300 and 400 torr. Numerical simulations of the same experiments were carried out using a detailed chemical kinetic reaction mechanism. The results are interpreted in terms of a low-temperature oxidation mechanism involving addition of molecular oxygen to alkyl and hydroperoxyalkyl radicals. Results indicate that in most cases, the reactive gases experience a two-stage autoignition. The first stage follows a low-temperature alkylperoxy radical isomerization pathway that is effectively quenched when the temperature reaches a level where dissociation reactions of alkylperoxy and hydroperoxyalkylperoxy radicals are more rapid than the reverse addition steps. The second stage is controlled by the onset of dissociation of hydrogen peroxide. At the highest compression temperatures achieved, little or no first-stage ignition is observed. Particular attention is given to the influence of heat transfer and the importance of regions of variable temperature within the compressed gas volume. Implications of this work on practical ignition problems are discussed.</description><identifier>ISSN: 1540-7489</identifier><identifier>EISSN: 1873-2704</identifier><identifier>DOI: 10.1016/S0082-0784(00)80566-4</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ADVANCED PROPULSION SYSTEMS ; ANTIKNOCK RATINGS ; COMBUSTION ; ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION ; ENGINES ; HYDROCARBONS ; IGNITION ; INTERNAL COMBUSTION ENGINES ; ISOMERIZATION ; ISOMERS ; KINETICS ; MOLECULAR STRUCTURE ; OXIDATION ; PENTANE ; PULSE COMBUSTORS ; SIMULATION</subject><ispartof>Proceedings of the Combustion Institute, 2000-01, Vol.28 (2), p.1671-1678</ispartof><rights>2000 Combustion Institute</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273</citedby><cites>FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,309,314,780,784,789,885,23930,27924,27925</link.rule.ids><backlink>$$Uhttps://www.osti.gov/servlets/purl/15008099$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Ribaucour, M.</creatorcontrib><creatorcontrib>Minetti, R.</creatorcontrib><creatorcontrib>Sochet, L.R.</creatorcontrib><creatorcontrib>Curran, H.J.</creatorcontrib><creatorcontrib>Pitz, W.J.</creatorcontrib><creatorcontrib>Westbrook, C.K.</creatorcontrib><creatorcontrib>Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)</creatorcontrib><title>Ignition of isomers of pentane: An experimental and kinetic modeling study</title><title>Proceedings of the Combustion Institute</title><description>Experiments in a rapid compression machine were used to examine the influences of variations in fuel molecular structure on the autoignition of isomers of pentane. Autoignition of stoichiometric mixtures of the three isomers of pentane were studied at compressed gas initial temperatures between 640 K and 900 K and at precompression pressures of 300 and 400 torr. Numerical simulations of the same experiments were carried out using a detailed chemical kinetic reaction mechanism. The results are interpreted in terms of a low-temperature oxidation mechanism involving addition of molecular oxygen to alkyl and hydroperoxyalkyl radicals. Results indicate that in most cases, the reactive gases experience a two-stage autoignition. The first stage follows a low-temperature alkylperoxy radical isomerization pathway that is effectively quenched when the temperature reaches a level where dissociation reactions of alkylperoxy and hydroperoxyalkylperoxy radicals are more rapid than the reverse addition steps. The second stage is controlled by the onset of dissociation of hydrogen peroxide. At the highest compression temperatures achieved, little or no first-stage ignition is observed. Particular attention is given to the influence of heat transfer and the importance of regions of variable temperature within the compressed gas volume. Implications of this work on practical ignition problems are discussed.</description><subject>ADVANCED PROPULSION SYSTEMS</subject><subject>ANTIKNOCK RATINGS</subject><subject>COMBUSTION</subject><subject>ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION</subject><subject>ENGINES</subject><subject>HYDROCARBONS</subject><subject>IGNITION</subject><subject>INTERNAL COMBUSTION ENGINES</subject><subject>ISOMERIZATION</subject><subject>ISOMERS</subject><subject>KINETICS</subject><subject>MOLECULAR STRUCTURE</subject><subject>OXIDATION</subject><subject>PENTANE</subject><subject>PULSE COMBUSTORS</subject><subject>SIMULATION</subject><issn>1540-7489</issn><issn>1873-2704</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqXwCUiW2MAiME7s2GGDqopHUSUWwNpynEkxtHYVm4r-PUnLntVczeNezSHknME1A1bevAKoPAOp-CXAlQJRlhk_ICOmZJHlEvhhrwWHTHJVHZOTGD8BCgmFGJHn2cK75IKnoaUuhhV2cZBr9Ml4vKUTT_FnjZ1bDZ0lNb6hX85jcpauQoNL5xc0pu9me0qOWrOMePZXx-T94f5t-pTNXx5n08k8s1xAyoyVVcHQ1k3e1gZLlIVsBSjJjDS85KrsZ1IYVpVK5HXLci5qLsFWtUDIZTEmF3vfEJPT0bqE9sMG79EmzUQPA6qq3xL7LduFGDts9br_wXRbzUAP2PQOmx6waQC9w6Z5f3e3v8P-hY3DbkhAb7Fx3RDQBPePwy90GnQk</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Ribaucour, M.</creator><creator>Minetti, R.</creator><creator>Sochet, L.R.</creator><creator>Curran, H.J.</creator><creator>Pitz, W.J.</creator><creator>Westbrook, C.K.</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OIOZB</scope><scope>OTOTI</scope></search><sort><creationdate>20000101</creationdate><title>Ignition of isomers of pentane: An experimental and kinetic modeling study</title><author>Ribaucour, M. ; Minetti, R. ; Sochet, L.R. ; Curran, H.J. ; Pitz, W.J. ; Westbrook, C.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>ADVANCED PROPULSION SYSTEMS</topic><topic>ANTIKNOCK RATINGS</topic><topic>COMBUSTION</topic><topic>ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION</topic><topic>ENGINES</topic><topic>HYDROCARBONS</topic><topic>IGNITION</topic><topic>INTERNAL COMBUSTION ENGINES</topic><topic>ISOMERIZATION</topic><topic>ISOMERS</topic><topic>KINETICS</topic><topic>MOLECULAR STRUCTURE</topic><topic>OXIDATION</topic><topic>PENTANE</topic><topic>PULSE COMBUSTORS</topic><topic>SIMULATION</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ribaucour, M.</creatorcontrib><creatorcontrib>Minetti, R.</creatorcontrib><creatorcontrib>Sochet, L.R.</creatorcontrib><creatorcontrib>Curran, H.J.</creatorcontrib><creatorcontrib>Pitz, W.J.</creatorcontrib><creatorcontrib>Westbrook, C.K.</creatorcontrib><creatorcontrib>Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Proceedings of the Combustion Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ribaucour, M.</au><au>Minetti, R.</au><au>Sochet, L.R.</au><au>Curran, H.J.</au><au>Pitz, W.J.</au><au>Westbrook, C.K.</au><aucorp>Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ignition of isomers of pentane: An experimental and kinetic modeling study</atitle><jtitle>Proceedings of the Combustion Institute</jtitle><date>2000-01-01</date><risdate>2000</risdate><volume>28</volume><issue>2</issue><spage>1671</spage><epage>1678</epage><pages>1671-1678</pages><issn>1540-7489</issn><eissn>1873-2704</eissn><abstract>Experiments in a rapid compression machine were used to examine the influences of variations in fuel molecular structure on the autoignition of isomers of pentane. Autoignition of stoichiometric mixtures of the three isomers of pentane were studied at compressed gas initial temperatures between 640 K and 900 K and at precompression pressures of 300 and 400 torr. Numerical simulations of the same experiments were carried out using a detailed chemical kinetic reaction mechanism. The results are interpreted in terms of a low-temperature oxidation mechanism involving addition of molecular oxygen to alkyl and hydroperoxyalkyl radicals. Results indicate that in most cases, the reactive gases experience a two-stage autoignition. The first stage follows a low-temperature alkylperoxy radical isomerization pathway that is effectively quenched when the temperature reaches a level where dissociation reactions of alkylperoxy and hydroperoxyalkylperoxy radicals are more rapid than the reverse addition steps. The second stage is controlled by the onset of dissociation of hydrogen peroxide. At the highest compression temperatures achieved, little or no first-stage ignition is observed. Particular attention is given to the influence of heat transfer and the importance of regions of variable temperature within the compressed gas volume. Implications of this work on practical ignition problems are discussed.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><doi>10.1016/S0082-0784(00)80566-4</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1540-7489 |
ispartof | Proceedings of the Combustion Institute, 2000-01, Vol.28 (2), p.1671-1678 |
issn | 1540-7489 1873-2704 |
language | eng |
recordid | cdi_osti_scitechconnect_15008099 |
source | ScienceDirect Journals |
subjects | ADVANCED PROPULSION SYSTEMS ANTIKNOCK RATINGS COMBUSTION ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION ENGINES HYDROCARBONS IGNITION INTERNAL COMBUSTION ENGINES ISOMERIZATION ISOMERS KINETICS MOLECULAR STRUCTURE OXIDATION PENTANE PULSE COMBUSTORS SIMULATION |
title | Ignition of isomers of pentane: An experimental and kinetic modeling study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A44%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ignition%20of%20isomers%20of%20pentane:%20An%20experimental%20and%20kinetic%20modeling%20study&rft.jtitle=Proceedings%20of%20the%20Combustion%20Institute&rft.au=Ribaucour,%20M.&rft.aucorp=Lawrence%20Livermore%20National%20Lab.%20(LLNL),%20Livermore,%20CA%20(United%20States)&rft.date=2000-01-01&rft.volume=28&rft.issue=2&rft.spage=1671&rft.epage=1678&rft.pages=1671-1678&rft.issn=1540-7489&rft.eissn=1873-2704&rft_id=info:doi/10.1016/S0082-0784(00)80566-4&rft_dat=%3Celsevier_osti_%3ES0082078400805664%3C/elsevier_osti_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c450t-ac7931ecbd2fbae6e737f50871a7a46486ecb75a196852bf1245b470c9b5e0273%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 |