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A combustion chemistry study of tetramethylethylene in a laminar premixed low-pressure hydrogen flame
Institution:1. Institute of Combustion Technology, German Aerospace Center (DLR), Pfaffenwaldring 38-40, 70569 Stuttgart, Germany;2. Laboratory for Synchrotron Radiation and Femtochemistry, Paul Scherrer Institute, 5232 Villigen, Switzerland;3. Mass Spectrometry in Reactive Flows, University of Duisburg-Essen, Lotharstraße 1, 47057 Duisburg, Germany;4. Division 9, State Health Office, Nordbahnhofstraße 135, 70191 Stuttgart, Germany;5. Technical Thermodynamics, Paderborn University, 33098 Paderborn, Germany;1. King Abdullah University of Science and Engineering (KAUST), Clean Combustion Research Center, Physical Sciences and Engineering Division, Thuwal 23955-6900, Saudi Arabia;2. Molecular Science and Nano-Materials Lab, Institute for Computational Science and Technology, SBI Building, Quang Trung Software City, Tan Chanh Hiep Ward, District 12, Ho Chi Minh City, Vietnam;3. University of Science, Vietnam National University – HCMC, 227 Nguyen Van Cu, Ward 4, District 5, Ho Chi Minh City, Vietnam;4. Vietnam National University – HCMC, Quarter 6, Linh Trung Ward, Thu Duc City, Ho Chi Minh City, Vietnam;5. International University, Quarter 6, Linh Trung Ward, Thu Duc City, Ho Chi Minh City, Vietnam;1. Chair of High Pressure Gas Dynamics, Shock Wave Laboratory, RWTH Aachen University, Aachen 52056, Germany;2. Institute of Technical Thermodynamics, RWTH Aachen University, Aachen 52056, Germany;3. DRIVE EA1859, Université de Bourgogne Franche-Comté, 49 Rue Mademoiselle Bourgeois, Nevers 58000, France;4. IRCER, UMR CNRS 7315, Université de Limoges, Limoges 87032, France;1. Key Laboratory for Power Machinery and Engineering of MOE, School of Mechanical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China;2. Clean Combustion Research Center, King Abdullah University of Science and Technology, Thuwal, 23955, Kingdom of Saudi Arabia;1. Department of Chemistry, University of Helsinki, P.O. Box 55 (A.I. Virtasen aukio 1), Helsinki 00014, Finland;2. Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Magyar Tudósok krt. 2., Budapest H-1117, Hungary;3. Chair of High Pressure Gas Dynamics, Shock Wave Laboratory, RWTH Aachen University, Aachen 52056, Germany
Abstract:The combustion chemistry of tetramethylethylene (TME) was studied in a premixed laminar low-pressure hydrogen flame by combined photoionization molecular-beam mass spectrometry (PI-MBMS) and photoelectron photoion coincidence (PEPICO) spectroscopy at the Swiss Light Source (SLS) of the Paul Scherrer Institute in Villigen, Switzerland. This hexene isomer with the chemical formula C6H12 has a special structure with only allylic Csingle bondH bonds. Several combustion intermediate species were identified by their photoionization and threshold photoelectron spectra, respectively. The experimental mole fraction profiles were compared to modeling results from a recently published kinetic reaction mechanism that includes a TME sub-mechanism to describe the TME/H2 flame structure. The first stable intermediate species formed early in the flame front during the combustion of TME are 2-methyl-2-butene (C5H10) at a mass-to-charge ratio (m/z) of 70, 2,3-dimethylbutane (C6H14) at m/z 86, and 3-methyl-1,2-butadiene (C5H8) at m/z 68. Isobutene (C4H8) is also a dominant intermediate in the combustion of TME and results from consumption of 2-methyl-2-butene. In addition to these hydrocarbons, some oxygenated species are formed due to low-temperature combustion chemistry in the consumption pathway of TME under the investigated flame conditions.
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