Catalytic activity of metal oxides supported on graphene oxide in oxidative desulfurization and denitrogenation
In this work, the effect of different parameters on catalyst efficiency in the catalytic oxidative desulfurization (ODS) and denitrogenation (ODN) process is studied. A series of samples with different metal compounds, including Ni, Cu, Co, CoNi, CoCu, and CuNi on a reduced graphene oxide (GO) we...
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description | In this work, the effect of different parameters on catalyst efficiency in the catalytic oxidative desulfurization (ODS) and denitrogenation (ODN) process is studied. A series of samples with different metal compounds, including Ni, Cu, Co, CoNi, CoCu, and CuNi on a reduced graphene oxide (GO) were prepared by an impregnation method. The synthesized samples were carefully characterized by Fourier transform infrared (FTIR), field emission scanning electron microscopy (FESEM), X‐ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) analysis, and X‐ray powder diffraction (XRD) techniques. The potential of this methodology was illustrated by the oxidation of 84.11% carbazole (CBZ) and 88.36% dibenzothiophene (DBT) in model fuel containing 500 ppmw sulfur and nitrogen. The effect of DBT and CBZ initial concentration and oxidant type on the oxidation process was investigated. The initial concentration of 250 ppmw for DBT and 100 ppmw for CBZ showed more efficiency than other initial concentrations (1,000, 750, 500, 250 ppmw) for DBT and (500, 400, 250, 100 ppmw) for CBZ, and NaClO as an oxidant showed higher performance than H
2
O
2
, formic acid, and oxygen. The results indicated that the Co‐Cu/rGO catalyst shows higher activity than other prepared catalysts in the oxidation of DBT and CBZ. Moreover, the catalyst could be regenerated three times with no discernible decrease in its catalytic activity. Lastly, the catalytic oxidation of CBZ and DBT was the proposed reaction mechanism. |
doi_str_mv | 10.1002/aoc.7272 |
format | Article |
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2
O
2
, formic acid, and oxygen. The results indicated that the Co‐Cu/rGO catalyst shows higher activity than other prepared catalysts in the oxidation of DBT and CBZ. Moreover, the catalyst could be regenerated three times with no discernible decrease in its catalytic activity. Lastly, the catalytic oxidation of CBZ and DBT was the proposed reaction mechanism.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.7272</identifier><language>eng</language><publisher>Chichester: Wiley Subscription Services, Inc</publisher><subject>Carbazoles ; Catalysts ; Catalytic activity ; Catalytic oxidation ; Chemistry ; Copper ; Denitrogenation ; Desulfurizing ; Dibenzothiophene ; Field emission microscopy ; Formic acid ; Fourier transforms ; Graphene ; Hydrogen peroxide ; Metal compounds ; Metal oxides ; Metals ; Nickel compounds ; Oxidation ; Oxidizing agents ; Photoelectrons ; Reaction mechanisms</subject><ispartof>Applied organometallic chemistry, 2023-11, Vol.37 (11)</ispartof><rights>2023 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c250t-f9cfc4b6b9502cd13661098a32917cadfac2255cbb631cef3e9ae2915192bac43</cites><orcidid>0000-0002-5428-2512 ; 0000-0002-8137-499X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Shadmehri, Mehdi A.</creatorcontrib><creatorcontrib>Housaindokht, Mohammad Reza</creatorcontrib><creatorcontrib>Nakhaei Pour, Ali</creatorcontrib><title>Catalytic activity of metal oxides supported on graphene oxide in oxidative desulfurization and denitrogenation</title><title>Applied organometallic chemistry</title><description>In this work, the effect of different parameters on catalyst efficiency in the catalytic oxidative desulfurization (ODS) and denitrogenation (ODN) process is studied. A series of samples with different metal compounds, including Ni, Cu, Co, CoNi, CoCu, and CuNi on a reduced graphene oxide (GO) were prepared by an impregnation method. The synthesized samples were carefully characterized by Fourier transform infrared (FTIR), field emission scanning electron microscopy (FESEM), X‐ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) analysis, and X‐ray powder diffraction (XRD) techniques. The potential of this methodology was illustrated by the oxidation of 84.11% carbazole (CBZ) and 88.36% dibenzothiophene (DBT) in model fuel containing 500 ppmw sulfur and nitrogen. The effect of DBT and CBZ initial concentration and oxidant type on the oxidation process was investigated. The initial concentration of 250 ppmw for DBT and 100 ppmw for CBZ showed more efficiency than other initial concentrations (1,000, 750, 500, 250 ppmw) for DBT and (500, 400, 250, 100 ppmw) for CBZ, and NaClO as an oxidant showed higher performance than H
2
O
2
, formic acid, and oxygen. The results indicated that the Co‐Cu/rGO catalyst shows higher activity than other prepared catalysts in the oxidation of DBT and CBZ. Moreover, the catalyst could be regenerated three times with no discernible decrease in its catalytic activity. Lastly, the catalytic oxidation of CBZ and DBT was the proposed reaction mechanism.</description><subject>Carbazoles</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Catalytic oxidation</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Denitrogenation</subject><subject>Desulfurizing</subject><subject>Dibenzothiophene</subject><subject>Field emission microscopy</subject><subject>Formic acid</subject><subject>Fourier transforms</subject><subject>Graphene</subject><subject>Hydrogen peroxide</subject><subject>Metal compounds</subject><subject>Metal oxides</subject><subject>Metals</subject><subject>Nickel compounds</subject><subject>Oxidation</subject><subject>Oxidizing agents</subject><subject>Photoelectrons</subject><subject>Reaction mechanisms</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNotkE1LAzEQhoMoWKvgTwh48bI1H93s5ihFq1Dwoucwm01qSpusSVasv9609TQz7zwzw7wI3VIyo4SwBwh61rCGnaEJJVJWpOHyHE0IE23FBKkv0VVKG0KIFHQ-QWEBGbb77DQGnd23y3scLN6ZouLw43qTcBqHIcRsehw8XkcYPo03pyZ2_phAGTW4wOPWjtH9lrqw4PuieZdjWBt_1K7RhYVtMjf_cYo-np_eFy_V6m35unhcVZrVJFdWaqvnnehkTZjuKReifNMCZ5I2GnoLmrG61l0nONXGciPBlF5NJetAz_kU3Z32DjF8jSZltQlj9OWkYm0jW04KXKj7E6VjSCkaq4bodhD3ihJ1sFMVO9XBTv4HYsRq2Q</recordid><startdate>202311</startdate><enddate>202311</enddate><creator>Shadmehri, Mehdi A.</creator><creator>Housaindokht, Mohammad Reza</creator><creator>Nakhaei Pour, Ali</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-5428-2512</orcidid><orcidid>https://orcid.org/0000-0002-8137-499X</orcidid></search><sort><creationdate>202311</creationdate><title>Catalytic activity of metal oxides supported on graphene oxide in oxidative desulfurization and denitrogenation</title><author>Shadmehri, Mehdi A. ; Housaindokht, Mohammad Reza ; Nakhaei Pour, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c250t-f9cfc4b6b9502cd13661098a32917cadfac2255cbb631cef3e9ae2915192bac43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Carbazoles</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Catalytic oxidation</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Denitrogenation</topic><topic>Desulfurizing</topic><topic>Dibenzothiophene</topic><topic>Field emission microscopy</topic><topic>Formic acid</topic><topic>Fourier transforms</topic><topic>Graphene</topic><topic>Hydrogen peroxide</topic><topic>Metal compounds</topic><topic>Metal oxides</topic><topic>Metals</topic><topic>Nickel compounds</topic><topic>Oxidation</topic><topic>Oxidizing agents</topic><topic>Photoelectrons</topic><topic>Reaction mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shadmehri, Mehdi A.</creatorcontrib><creatorcontrib>Housaindokht, Mohammad Reza</creatorcontrib><creatorcontrib>Nakhaei Pour, Ali</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied organometallic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shadmehri, Mehdi A.</au><au>Housaindokht, Mohammad Reza</au><au>Nakhaei Pour, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalytic activity of metal oxides supported on graphene oxide in oxidative desulfurization and denitrogenation</atitle><jtitle>Applied organometallic chemistry</jtitle><date>2023-11</date><risdate>2023</risdate><volume>37</volume><issue>11</issue><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>In this work, the effect of different parameters on catalyst efficiency in the catalytic oxidative desulfurization (ODS) and denitrogenation (ODN) process is studied. A series of samples with different metal compounds, including Ni, Cu, Co, CoNi, CoCu, and CuNi on a reduced graphene oxide (GO) were prepared by an impregnation method. The synthesized samples were carefully characterized by Fourier transform infrared (FTIR), field emission scanning electron microscopy (FESEM), X‐ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) analysis, and X‐ray powder diffraction (XRD) techniques. The potential of this methodology was illustrated by the oxidation of 84.11% carbazole (CBZ) and 88.36% dibenzothiophene (DBT) in model fuel containing 500 ppmw sulfur and nitrogen. The effect of DBT and CBZ initial concentration and oxidant type on the oxidation process was investigated. The initial concentration of 250 ppmw for DBT and 100 ppmw for CBZ showed more efficiency than other initial concentrations (1,000, 750, 500, 250 ppmw) for DBT and (500, 400, 250, 100 ppmw) for CBZ, and NaClO as an oxidant showed higher performance than H
2
O
2
, formic acid, and oxygen. The results indicated that the Co‐Cu/rGO catalyst shows higher activity than other prepared catalysts in the oxidation of DBT and CBZ. Moreover, the catalyst could be regenerated three times with no discernible decrease in its catalytic activity. Lastly, the catalytic oxidation of CBZ and DBT was the proposed reaction mechanism.</abstract><cop>Chichester</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aoc.7272</doi><orcidid>https://orcid.org/0000-0002-5428-2512</orcidid><orcidid>https://orcid.org/0000-0002-8137-499X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Carbazoles Catalysts Catalytic activity Catalytic oxidation Chemistry Copper Denitrogenation Desulfurizing Dibenzothiophene Field emission microscopy Formic acid Fourier transforms Graphene Hydrogen peroxide Metal compounds Metal oxides Metals Nickel compounds Oxidation Oxidizing agents Photoelectrons Reaction mechanisms |
title | Catalytic activity of metal oxides supported on graphene oxide in oxidative desulfurization and denitrogenation |
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