Methane conversion by repetitive nanosecond pulsed plasma
A detailed study of methane conversion by repetitive nanosecond pulsed plasma was accomplished. In this study, a conversion rate of about 60% was obtained at an energy conversion efficiency of more than 75%. The conversion performance reached the optimum value at an electrode gap of about 5 mm. To r...
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Veröffentlicht in: | Journal of physics. D, Applied physics Applied physics, 2014-09, Vol.47 (36), p.1-16 |
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description | A detailed study of methane conversion by repetitive nanosecond pulsed plasma was accomplished. In this study, a conversion rate of about 60% was obtained at an energy conversion efficiency of more than 75%. The conversion performance reached the optimum value at an electrode gap of about 5 mm. To raise the temperature, the reactor was thermally isolated. At moderate frequencies, a non-isolated reactor with a lower temperature demonstrated a better conversion performance. This was attributed to the dominance of the vibrational dissociation channel. It was also demonstrated that the conversion process considerably improved at a pulse-to-pulse time interval of less than 100 µs, which is the lifetime of ion molecules at atmospheric pressure. A mathematical model based on two temperatures is developed in order to explain the dissociation mechanism. The model reveals that the greatest molecular dissociation occurs when there is a high vibrational non-equilibrium state in the molecule. This non-equilibrium state lasts less than a microsecond at the post-plasma stage. It explains the high efficiencies obtained in the conversion process and is specific to the pulsed plasmas. |
doi_str_mv | 10.1088/0022-3727/47/36/365201 |
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In this study, a conversion rate of about 60% was obtained at an energy conversion efficiency of more than 75%. The conversion performance reached the optimum value at an electrode gap of about 5 mm. To raise the temperature, the reactor was thermally isolated. At moderate frequencies, a non-isolated reactor with a lower temperature demonstrated a better conversion performance. This was attributed to the dominance of the vibrational dissociation channel. It was also demonstrated that the conversion process considerably improved at a pulse-to-pulse time interval of less than 100 µs, which is the lifetime of ion molecules at atmospheric pressure. A mathematical model based on two temperatures is developed in order to explain the dissociation mechanism. The model reveals that the greatest molecular dissociation occurs when there is a high vibrational non-equilibrium state in the molecule. This non-equilibrium state lasts less than a microsecond at the post-plasma stage. It explains the high efficiencies obtained in the conversion process and is specific to the pulsed plasmas.</description><identifier>ISSN: 0022-3727</identifier><identifier>EISSN: 1361-6463</identifier><identifier>DOI: 10.1088/0022-3727/47/36/365201</identifier><identifier>CODEN: JPAPBE</identifier><language>eng</language><publisher>IOP Publishing</publisher><subject>Conversion ; Dominance ; efficiency ; Electrodes ; Mathematical models ; Methane ; methane conversion ; molecular vibrations ; Nanostructure ; Plasma (physics) ; pulsed plasma ; Reactors</subject><ispartof>Journal of physics. 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D, Applied physics</title><addtitle>JPhysD</addtitle><addtitle>J. Phys. D: Appl. Phys</addtitle><description>A detailed study of methane conversion by repetitive nanosecond pulsed plasma was accomplished. In this study, a conversion rate of about 60% was obtained at an energy conversion efficiency of more than 75%. The conversion performance reached the optimum value at an electrode gap of about 5 mm. To raise the temperature, the reactor was thermally isolated. At moderate frequencies, a non-isolated reactor with a lower temperature demonstrated a better conversion performance. This was attributed to the dominance of the vibrational dissociation channel. It was also demonstrated that the conversion process considerably improved at a pulse-to-pulse time interval of less than 100 µs, which is the lifetime of ion molecules at atmospheric pressure. A mathematical model based on two temperatures is developed in order to explain the dissociation mechanism. The model reveals that the greatest molecular dissociation occurs when there is a high vibrational non-equilibrium state in the molecule. This non-equilibrium state lasts less than a microsecond at the post-plasma stage. It explains the high efficiencies obtained in the conversion process and is specific to the pulsed plasmas.</description><subject>Conversion</subject><subject>Dominance</subject><subject>efficiency</subject><subject>Electrodes</subject><subject>Mathematical models</subject><subject>Methane</subject><subject>methane conversion</subject><subject>molecular vibrations</subject><subject>Nanostructure</subject><subject>Plasma (physics)</subject><subject>pulsed plasma</subject><subject>Reactors</subject><issn>0022-3727</issn><issn>1361-6463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkE9LxDAQxYMouK5-BenRS90kTSfpURb_geJFzyFNJ9il29SkXdhvb0rFq0JgSOa9yZsfIdeM3jKq1IZSzvNCcrkRclNAOiWn7ISsWAEsBwHFKVn9is7JRYw7SmkJiq1I9Yrjp-kxs74_YIit77P6mAUccGzH9oBZb3ofMbWbbJi6iKl0Ju7NJTlzJt2vfuqafDzcv2-f8pe3x-ft3UtuBcgxt-kjUHVtOKe2EQ0vsVGOOodSOSO4w1qlvFVpoYGGoVDSoajSixRAayjW5GaZOwT_NWEc9b6NFrsupfZT1AykokxK-R8prxITKGcpLFIbfIwBnR5CuzfhqBnVM1Y9E9MzMS2kLkAvWJORL8bWD3rnp9Cn5f8yfQNyE3kB</recordid><startdate>20140910</startdate><enddate>20140910</enddate><creator>Lotfalipour, R</creator><creator>Ghorbanzadeh, A M</creator><creator>Mahdian, A</creator><general>IOP Publishing</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20140910</creationdate><title>Methane conversion by repetitive nanosecond pulsed plasma</title><author>Lotfalipour, R ; Ghorbanzadeh, A M ; Mahdian, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-c05668bba220cd4d25ed8f0ffe78fa42feb852095c6d6d1e487fe492097460b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Conversion</topic><topic>Dominance</topic><topic>efficiency</topic><topic>Electrodes</topic><topic>Mathematical models</topic><topic>Methane</topic><topic>methane conversion</topic><topic>molecular vibrations</topic><topic>Nanostructure</topic><topic>Plasma (physics)</topic><topic>pulsed plasma</topic><topic>Reactors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lotfalipour, R</creatorcontrib><creatorcontrib>Ghorbanzadeh, A M</creatorcontrib><creatorcontrib>Mahdian, A</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of physics. D, Applied physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lotfalipour, R</au><au>Ghorbanzadeh, A M</au><au>Mahdian, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methane conversion by repetitive nanosecond pulsed plasma</atitle><jtitle>Journal of physics. D, Applied physics</jtitle><stitle>JPhysD</stitle><addtitle>J. Phys. D: Appl. Phys</addtitle><date>2014-09-10</date><risdate>2014</risdate><volume>47</volume><issue>36</issue><spage>1</spage><epage>16</epage><pages>1-16</pages><issn>0022-3727</issn><eissn>1361-6463</eissn><coden>JPAPBE</coden><abstract>A detailed study of methane conversion by repetitive nanosecond pulsed plasma was accomplished. In this study, a conversion rate of about 60% was obtained at an energy conversion efficiency of more than 75%. The conversion performance reached the optimum value at an electrode gap of about 5 mm. To raise the temperature, the reactor was thermally isolated. At moderate frequencies, a non-isolated reactor with a lower temperature demonstrated a better conversion performance. This was attributed to the dominance of the vibrational dissociation channel. It was also demonstrated that the conversion process considerably improved at a pulse-to-pulse time interval of less than 100 µs, which is the lifetime of ion molecules at atmospheric pressure. A mathematical model based on two temperatures is developed in order to explain the dissociation mechanism. The model reveals that the greatest molecular dissociation occurs when there is a high vibrational non-equilibrium state in the molecule. This non-equilibrium state lasts less than a microsecond at the post-plasma stage. 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subjects | Conversion Dominance efficiency Electrodes Mathematical models Methane methane conversion molecular vibrations Nanostructure Plasma (physics) pulsed plasma Reactors |
title | Methane conversion by repetitive nanosecond pulsed plasma |
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