An insight into Ru/TiO sub(2) catalyzed wet air oxidation of N-ethylethanolamine in an aqueous solution
The catalytic wet air oxidation of N-ethylethanolamine (EEA) over 5% (w/w) Ru/TiO sub(2) catalyst was investigated at 500 mg L super(-1) EEA concentration, in the temperature range of 423-473 K, O sub(2) partial pressure of 0.34-1.38 MPa and catalyst loading of 0.33-1.32 kg m super(-3) in a kinetica...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2010-05, Vol.159 (1-3), p.17-23 |
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creator | Gunale, Tukaram L Mahajani, Vijaykumar V |
description | The catalytic wet air oxidation of N-ethylethanolamine (EEA) over 5% (w/w) Ru/TiO sub(2) catalyst was investigated at 500 mg L super(-1) EEA concentration, in the temperature range of 423-473 K, O sub(2) partial pressure of 0.34-1.38 MPa and catalyst loading of 0.33-1.32 kg m super(-3) in a kinetically controlled regime. The fate of 'N' atom of EEA was also investigated. 5% Ru/TiO sub(2) was found to be effective catalyst for complete degradation of EEA and active in the conversion of -NH- group of EEA to N sub(2). The highest conversion of -NH- to N sub(2) was about 70% at 448 K. Under partial resistance to mass transfer the selectivity to N sub(2) was marginally enhanced. Ethylamine (EA) was formed as an intermediate and found to be relatively refractory. The kinetic data was modeled using the power law rate expression in terms of total organic carbon (TOC). The experimental data could be best correlated by Langmuir-Hinshelwood type reaction model involving dual site dissociative adsorption of O sub(2). |
doi_str_mv | 10.1016/j.cej.2010.02.015 |
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The fate of 'N' atom of EEA was also investigated. 5% Ru/TiO sub(2) was found to be effective catalyst for complete degradation of EEA and active in the conversion of -NH- group of EEA to N sub(2). The highest conversion of -NH- to N sub(2) was about 70% at 448 K. Under partial resistance to mass transfer the selectivity to N sub(2) was marginally enhanced. Ethylamine (EA) was formed as an intermediate and found to be relatively refractory. The kinetic data was modeled using the power law rate expression in terms of total organic carbon (TOC). 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The fate of 'N' atom of EEA was also investigated. 5% Ru/TiO sub(2) was found to be effective catalyst for complete degradation of EEA and active in the conversion of -NH- group of EEA to N sub(2). The highest conversion of -NH- to N sub(2) was about 70% at 448 K. Under partial resistance to mass transfer the selectivity to N sub(2) was marginally enhanced. Ethylamine (EA) was formed as an intermediate and found to be relatively refractory. The kinetic data was modeled using the power law rate expression in terms of total organic carbon (TOC). The experimental data could be best correlated by Langmuir-Hinshelwood type reaction model involving dual site dissociative adsorption of O sub(2).</description><subject>Active control</subject><subject>Carbon</subject><subject>Catalysts</subject><subject>Conversion</subject><subject>Mass transfer</subject><subject>Oxidation</subject><subject>Partial pressure</subject><subject>Titanium dioxide</subject><issn>1385-8947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNjM1uwjAQhH0oEhR4AG57a3tIsPNDkiOqWvUEEuKOlmASR8Zus7Zo-vR1pD5ApdGMRvpmGFsJHgsuNusurmUXJzx0nsRc5A9sJtIyj8oqK6bskajjnG8qUc1YszWgDKmmdSGdhYNfH9UeyJ-fkxeo0aEefuQF7tIBqh7st7qgU9aAvcIukq4ddDA0VuNNGRleAIO-vLSegKz2I71gkytqksu_nLOn97fj60f02duAkjvdFNVSazTj7lTkaZGlSVak_yd_AeLGT7s</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Gunale, Tukaram L</creator><creator>Mahajani, Vijaykumar V</creator><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20100501</creationdate><title>An insight into Ru/TiO sub(2) catalyzed wet air oxidation of N-ethylethanolamine in an aqueous solution</title><author>Gunale, Tukaram L ; Mahajani, Vijaykumar V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_7537432473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Active control</topic><topic>Carbon</topic><topic>Catalysts</topic><topic>Conversion</topic><topic>Mass transfer</topic><topic>Oxidation</topic><topic>Partial pressure</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gunale, Tukaram L</creatorcontrib><creatorcontrib>Mahajani, Vijaykumar V</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gunale, Tukaram L</au><au>Mahajani, Vijaykumar V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An insight into Ru/TiO sub(2) catalyzed wet air oxidation of N-ethylethanolamine in an aqueous solution</atitle><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle><date>2010-05-01</date><risdate>2010</risdate><volume>159</volume><issue>1-3</issue><spage>17</spage><epage>23</epage><pages>17-23</pages><issn>1385-8947</issn><abstract>The catalytic wet air oxidation of N-ethylethanolamine (EEA) over 5% (w/w) Ru/TiO sub(2) catalyst was investigated at 500 mg L super(-1) EEA concentration, in the temperature range of 423-473 K, O sub(2) partial pressure of 0.34-1.38 MPa and catalyst loading of 0.33-1.32 kg m super(-3) in a kinetically controlled regime. The fate of 'N' atom of EEA was also investigated. 5% Ru/TiO sub(2) was found to be effective catalyst for complete degradation of EEA and active in the conversion of -NH- group of EEA to N sub(2). The highest conversion of -NH- to N sub(2) was about 70% at 448 K. Under partial resistance to mass transfer the selectivity to N sub(2) was marginally enhanced. Ethylamine (EA) was formed as an intermediate and found to be relatively refractory. The kinetic data was modeled using the power law rate expression in terms of total organic carbon (TOC). The experimental data could be best correlated by Langmuir-Hinshelwood type reaction model involving dual site dissociative adsorption of O sub(2).</abstract><doi>10.1016/j.cej.2010.02.015</doi></addata></record> |
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subjects | Active control Carbon Catalysts Conversion Mass transfer Oxidation Partial pressure Titanium dioxide |
title | An insight into Ru/TiO sub(2) catalyzed wet air oxidation of N-ethylethanolamine in an aqueous solution |
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