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Theoretical Investigation of Rate Rules for H-Intermigration Reactions for Cyclic Alkylperoxy Radicals
As a starting channel, the H-intermigration reaction of alkylperoxy radicals (ROO radicals) that yields hydroperoxyl alkyl radicals (QOOH radicals) determines the low-temperature chemistry of alkanes. In this work, this type of reaction was investigated for typical cyclic alkanes, which are importan...
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Published in: | Energies (Basel) 2023-03, Vol.16 (6), p.2881 |
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description | As a starting channel, the H-intermigration reaction of alkylperoxy radicals (ROO radicals) that yields hydroperoxyl alkyl radicals (QOOH radicals) determines the low-temperature chemistry of alkanes. In this work, this type of reaction was investigated for typical cyclic alkanes, which are important fuel components and soot precursors, using theoretical ab initio methods. First, all the molecular geometries and vibrational frequencies were computed using the density functional theory method and the single point energies were refined using the post-Hartree fork method (M062X/6-311G(d,p)//DLPNO-CCSD(T)/CBS). Then, high-pressure limit rate constants were evaluated with tight transition state theory, with which tunneling effects were considered using the Eckart model and low-frequency torsion modes were modeled as hindered rotors. Pressure-dependent rate constants were also calculated for typical reaction channels. Rate expressions in the Arrhenius form for 91 reactions are proposed. All reactions were categorized into seven reaction types and the rate rule for each reaction type was estimated with uncertainty factors of three to six. These rules can be potentially used in the development of low-temperature kinetic mechanisms for cycloalkanes. A comparison between different reaction types was also performed and the favorable channels are discussed. |
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In this work, this type of reaction was investigated for typical cyclic alkanes, which are important fuel components and soot precursors, using theoretical ab initio methods. First, all the molecular geometries and vibrational frequencies were computed using the density functional theory method and the single point energies were refined using the post-Hartree fork method (M062X/6-311G(d,p)//DLPNO-CCSD(T)/CBS). Then, high-pressure limit rate constants were evaluated with tight transition state theory, with which tunneling effects were considered using the Eckart model and low-frequency torsion modes were modeled as hindered rotors. Pressure-dependent rate constants were also calculated for typical reaction channels. Rate expressions in the Arrhenius form for 91 reactions are proposed. All reactions were categorized into seven reaction types and the rate rule for each reaction type was estimated with uncertainty factors of three to six. These rules can be potentially used in the development of low-temperature kinetic mechanisms for cycloalkanes. A comparison between different reaction types was also performed and the favorable channels are discussed.</description><identifier>ISSN: 1996-1073</identifier><identifier>EISSN: 1996-1073</identifier><identifier>DOI: 10.3390/en16062881</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>ab initio calculation ; Alkanes ; Analysis ; Biodiesel fuels ; Biofuels ; Channels ; Chemistry ; cycloalkylperoxy radicals ; Decomposition ; Density functional theory ; Density functionals ; Energy ; H-intermigration reaction ; Hydrocarbons ; Investigations ; Low temperature ; Methods ; Oxidation ; Pressure dependence ; Radicals ; rate rules ; Rotors ; Vibrational spectra</subject><ispartof>Energies (Basel), 2023-03, Vol.16 (6), p.2881</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-1002024eeda52cca602b090e891d78ab8bcc0bbfd0c05a3be09a6fe8132749e73</citedby><cites>FETCH-LOGICAL-c400t-1002024eeda52cca602b090e891d78ab8bcc0bbfd0c05a3be09a6fe8132749e73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2791648926/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2791648926?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Yang, Kun</creatorcontrib><creatorcontrib>Tian, Zemin</creatorcontrib><creatorcontrib>Li, Jinghua</creatorcontrib><creatorcontrib>Yan, Yingwen</creatorcontrib><title>Theoretical Investigation of Rate Rules for H-Intermigration Reactions for Cyclic Alkylperoxy Radicals</title><title>Energies (Basel)</title><description>As a starting channel, the H-intermigration reaction of alkylperoxy radicals (ROO radicals) that yields hydroperoxyl alkyl radicals (QOOH radicals) determines the low-temperature chemistry of alkanes. In this work, this type of reaction was investigated for typical cyclic alkanes, which are important fuel components and soot precursors, using theoretical ab initio methods. First, all the molecular geometries and vibrational frequencies were computed using the density functional theory method and the single point energies were refined using the post-Hartree fork method (M062X/6-311G(d,p)//DLPNO-CCSD(T)/CBS). Then, high-pressure limit rate constants were evaluated with tight transition state theory, with which tunneling effects were considered using the Eckart model and low-frequency torsion modes were modeled as hindered rotors. Pressure-dependent rate constants were also calculated for typical reaction channels. Rate expressions in the Arrhenius form for 91 reactions are proposed. All reactions were categorized into seven reaction types and the rate rule for each reaction type was estimated with uncertainty factors of three to six. These rules can be potentially used in the development of low-temperature kinetic mechanisms for cycloalkanes. A comparison between different reaction types was also performed and the favorable channels are discussed.</description><subject>ab initio calculation</subject><subject>Alkanes</subject><subject>Analysis</subject><subject>Biodiesel fuels</subject><subject>Biofuels</subject><subject>Channels</subject><subject>Chemistry</subject><subject>cycloalkylperoxy radicals</subject><subject>Decomposition</subject><subject>Density functional theory</subject><subject>Density functionals</subject><subject>Energy</subject><subject>H-intermigration reaction</subject><subject>Hydrocarbons</subject><subject>Investigations</subject><subject>Low temperature</subject><subject>Methods</subject><subject>Oxidation</subject><subject>Pressure dependence</subject><subject>Radicals</subject><subject>rate rules</subject><subject>Rotors</subject><subject>Vibrational spectra</subject><issn>1996-1073</issn><issn>1996-1073</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUV1rGzEQPEoDCWle8gsO8hZwupLO-ng0pm0MgYJJnsVKt3Lknk-u7hzqfx-5F5JID7usZoZZTVVdM7gTwsB36pkEybVmX6oLZoycMVDi66f-vLoahi2UIwQTQlxU4fGZUqYxeuzqVf9Cwxg3OMbU1ynUaxypXh86GuqQcn0_W_Uj5V3c5AmyJvSnZnpeHn0Xfb3o_hy7PeX071gE2pPy8K06C6XQ1Vu9rJ5-_nhc3s8efv9aLRcPM98AjMUjcOANUYtz7j1K4A4MkDasVRqddt6Dc6EFD3MUjsCgDKSZ4KoxpMRltZp024Rbu89xh_loE0b7f5DyxmIuy3ZkNbjgZKOd5KLhQmivECV6IOVRh3nRupm09jn9PZSPsdt0yH2xb7kyrFANlwV1N6E2WERjH9KY0Zfb0i761FOIZb5QjVCyKREUwu1E8DkNQ6bwbpOBPeVoP3IUr1a6j-E</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Yang, Kun</creator><creator>Tian, Zemin</creator><creator>Li, Jinghua</creator><creator>Yan, Yingwen</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20230301</creationdate><title>Theoretical Investigation of Rate Rules for H-Intermigration Reactions for Cyclic Alkylperoxy Radicals</title><author>Yang, Kun ; Tian, Zemin ; Li, Jinghua ; Yan, Yingwen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-1002024eeda52cca602b090e891d78ab8bcc0bbfd0c05a3be09a6fe8132749e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>ab initio calculation</topic><topic>Alkanes</topic><topic>Analysis</topic><topic>Biodiesel fuels</topic><topic>Biofuels</topic><topic>Channels</topic><topic>Chemistry</topic><topic>cycloalkylperoxy radicals</topic><topic>Decomposition</topic><topic>Density functional theory</topic><topic>Density functionals</topic><topic>Energy</topic><topic>H-intermigration reaction</topic><topic>Hydrocarbons</topic><topic>Investigations</topic><topic>Low temperature</topic><topic>Methods</topic><topic>Oxidation</topic><topic>Pressure dependence</topic><topic>Radicals</topic><topic>rate rules</topic><topic>Rotors</topic><topic>Vibrational spectra</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Kun</creatorcontrib><creatorcontrib>Tian, Zemin</creatorcontrib><creatorcontrib>Li, Jinghua</creatorcontrib><creatorcontrib>Yan, Yingwen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Energies (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Kun</au><au>Tian, Zemin</au><au>Li, Jinghua</au><au>Yan, Yingwen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Theoretical Investigation of Rate Rules for H-Intermigration Reactions for Cyclic Alkylperoxy Radicals</atitle><jtitle>Energies (Basel)</jtitle><date>2023-03-01</date><risdate>2023</risdate><volume>16</volume><issue>6</issue><spage>2881</spage><pages>2881-</pages><issn>1996-1073</issn><eissn>1996-1073</eissn><abstract>As a starting channel, the H-intermigration reaction of alkylperoxy radicals (ROO radicals) that yields hydroperoxyl alkyl radicals (QOOH radicals) determines the low-temperature chemistry of alkanes. In this work, this type of reaction was investigated for typical cyclic alkanes, which are important fuel components and soot precursors, using theoretical ab initio methods. First, all the molecular geometries and vibrational frequencies were computed using the density functional theory method and the single point energies were refined using the post-Hartree fork method (M062X/6-311G(d,p)//DLPNO-CCSD(T)/CBS). Then, high-pressure limit rate constants were evaluated with tight transition state theory, with which tunneling effects were considered using the Eckart model and low-frequency torsion modes were modeled as hindered rotors. Pressure-dependent rate constants were also calculated for typical reaction channels. Rate expressions in the Arrhenius form for 91 reactions are proposed. All reactions were categorized into seven reaction types and the rate rule for each reaction type was estimated with uncertainty factors of three to six. These rules can be potentially used in the development of low-temperature kinetic mechanisms for cycloalkanes. A comparison between different reaction types was also performed and the favorable channels are discussed.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/en16062881</doi><oa>free_for_read</oa></addata></record> |
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subjects | ab initio calculation Alkanes Analysis Biodiesel fuels Biofuels Channels Chemistry cycloalkylperoxy radicals Decomposition Density functional theory Density functionals Energy H-intermigration reaction Hydrocarbons Investigations Low temperature Methods Oxidation Pressure dependence Radicals rate rules Rotors Vibrational spectra |
title | Theoretical Investigation of Rate Rules for H-Intermigration Reactions for Cyclic Alkylperoxy Radicals |
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