Zhaohan Chu , Zhongkai Liu , Changyang Wang , Long Zhao , Bin Yang
{"title":"邻甲基苯基自由基+ C2H2/C2H4反应生成茚的实验证据","authors":"Zhaohan Chu , Zhongkai Liu , Changyang Wang , Long Zhao , Bin Yang","doi":"10.1016/j.proci.2025.105859","DOIUrl":null,"url":null,"abstract":"<div><div>An experimental study was conducted to investigate the weight growth routes from <em>o</em>-methylphenyl radical (<em>o</em>-CH<sub>3</sub>C<sub>6</sub>H<sub>4</sub>) to indene. <em>o</em>-Nitrosotoluene served as the precursor for <em>o</em>-methylphenyl radicals in this study. Co-pyrolysis of <em>o</em>-methylphenyl radical/C<sub>2</sub>H<sub>2</sub> and <em>o</em>-methylphenyl radical/C<sub>2</sub>H<sub>4</sub> was investigated utilizing the chemical microreactor and synchrotron vacuum ultraviolet photoionization mass spectrometry. Sampled mass-specific photoionization efficiency (PIE) curves were employed to identify the aromatic species, elucidating interactions between <em>o</em>-methylphenyl radicals and C<sub>2</sub> species. The species detected at <em>m/z</em> = 116 and 118, essential for understanding the reaction mechanism, were identified via matching photoionization cross-sections and adiabatic ionization energies with literature and theoretical values. Specifically, indene and its isomer <em>o</em>-methylphenylacetylene (<em>m/z</em> = 116) were determined in the reaction of <em>o</em>-methylphenyl radical with C<sub>2</sub>H<sub>2</sub>, while indene and <em>o</em>-methylstyrene (<em>m/z</em> = 118) were identified in the reaction of <em>o</em>-methylphenyl radical with C<sub>2</sub>H<sub>4</sub>. By combining the identified intermediate species with previous literature basis, the formation pathways for indene, originating from <em>o</em>-methylphenyl radical were discussed in both reaction systems, providing further insights for understanding the indene formation pathways.</div></div>","PeriodicalId":408,"journal":{"name":"Proceedings of the Combustion Institute","volume":"41 ","pages":"Article 105859"},"PeriodicalIF":5.2000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Experimental evidence for indene formation from o-methylphenyl radical + C2H2/C2H4 reactions\",\"authors\":\"Zhaohan Chu , Zhongkai Liu , Changyang Wang , Long Zhao , Bin Yang\",\"doi\":\"10.1016/j.proci.2025.105859\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An experimental study was conducted to investigate the weight growth routes from <em>o</em>-methylphenyl radical (<em>o</em>-CH<sub>3</sub>C<sub>6</sub>H<sub>4</sub>) to indene. <em>o</em>-Nitrosotoluene served as the precursor for <em>o</em>-methylphenyl radicals in this study. Co-pyrolysis of <em>o</em>-methylphenyl radical/C<sub>2</sub>H<sub>2</sub> and <em>o</em>-methylphenyl radical/C<sub>2</sub>H<sub>4</sub> was investigated utilizing the chemical microreactor and synchrotron vacuum ultraviolet photoionization mass spectrometry. Sampled mass-specific photoionization efficiency (PIE) curves were employed to identify the aromatic species, elucidating interactions between <em>o</em>-methylphenyl radicals and C<sub>2</sub> species. The species detected at <em>m/z</em> = 116 and 118, essential for understanding the reaction mechanism, were identified via matching photoionization cross-sections and adiabatic ionization energies with literature and theoretical values. Specifically, indene and its isomer <em>o</em>-methylphenylacetylene (<em>m/z</em> = 116) were determined in the reaction of <em>o</em>-methylphenyl radical with C<sub>2</sub>H<sub>2</sub>, while indene and <em>o</em>-methylstyrene (<em>m/z</em> = 118) were identified in the reaction of <em>o</em>-methylphenyl radical with C<sub>2</sub>H<sub>4</sub>. By combining the identified intermediate species with previous literature basis, the formation pathways for indene, originating from <em>o</em>-methylphenyl radical were discussed in both reaction systems, providing further insights for understanding the indene formation pathways.</div></div>\",\"PeriodicalId\":408,\"journal\":{\"name\":\"Proceedings of the Combustion Institute\",\"volume\":\"41 \",\"pages\":\"Article 105859\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the Combustion Institute\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1540748925000732\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Combustion Institute","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1540748925000732","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Experimental evidence for indene formation from o-methylphenyl radical + C2H2/C2H4 reactions
An experimental study was conducted to investigate the weight growth routes from o-methylphenyl radical (o-CH3C6H4) to indene. o-Nitrosotoluene served as the precursor for o-methylphenyl radicals in this study. Co-pyrolysis of o-methylphenyl radical/C2H2 and o-methylphenyl radical/C2H4 was investigated utilizing the chemical microreactor and synchrotron vacuum ultraviolet photoionization mass spectrometry. Sampled mass-specific photoionization efficiency (PIE) curves were employed to identify the aromatic species, elucidating interactions between o-methylphenyl radicals and C2 species. The species detected at m/z = 116 and 118, essential for understanding the reaction mechanism, were identified via matching photoionization cross-sections and adiabatic ionization energies with literature and theoretical values. Specifically, indene and its isomer o-methylphenylacetylene (m/z = 116) were determined in the reaction of o-methylphenyl radical with C2H2, while indene and o-methylstyrene (m/z = 118) were identified in the reaction of o-methylphenyl radical with C2H4. By combining the identified intermediate species with previous literature basis, the formation pathways for indene, originating from o-methylphenyl radical were discussed in both reaction systems, providing further insights for understanding the indene formation pathways.
期刊介绍:
The Proceedings of the Combustion Institute contains forefront contributions in fundamentals and applications of combustion science. For more than 50 years, the Combustion Institute has served as the peak international society for dissemination of scientific and technical research in the combustion field. In addition to author submissions, the Proceedings of the Combustion Institute includes the Institute''s prestigious invited strategic and topical reviews that represent indispensable resources for emergent research in the field. All papers are subjected to rigorous peer review.
Research papers and invited topical reviews; Reaction Kinetics; Soot, PAH, and other large molecules; Diagnostics; Laminar Flames; Turbulent Flames; Heterogeneous Combustion; Spray and Droplet Combustion; Detonations, Explosions & Supersonic Combustion; Fire Research; Stationary Combustion Systems; IC Engine and Gas Turbine Combustion; New Technology Concepts
The electronic version of Proceedings of the Combustion Institute contains supplemental material such as reaction mechanisms, illustrating movies, and other data.