Catalytic decomposition of 1,3-diphenoxybenzene to monomeric cyclic compounds over palladium catalysts supported on acidic activated carbon aerogels

[Display omitted] ► Pd catalysts supported on acidic ACAs (activated carbon aerogels) were prepared. ► Catalytic decomposition of 1,3-diphenoxybenzene was conducted. ► Acidity of the catalysts played an important role in the reaction. ► Total yield for monomeric cyclic compounds increased with incre...

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Veröffentlicht in:Applied catalysis. A, General General, 2013-04, Vol.456, p.59-66
Hauptverfasser: Park, Hai Woong, Kim, Jeong Kwon, Hong, Ung Gi, Lee, Yoon Jae, Choi, Jung Ho, Bang, Yongju, Song, In Kyu
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container_title Applied catalysis. A, General
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creator Park, Hai Woong
Kim, Jeong Kwon
Hong, Ung Gi
Lee, Yoon Jae
Choi, Jung Ho
Bang, Yongju
Song, In Kyu
description [Display omitted] ► Pd catalysts supported on acidic ACAs (activated carbon aerogels) were prepared. ► Catalytic decomposition of 1,3-diphenoxybenzene was conducted. ► Acidity of the catalysts played an important role in the reaction. ► Total yield for monomeric cyclic compounds increased with increasing catalyst acidity. Activated carbon aerogel (ACA) was prepared by a chemical activation of carbon aerogel using phosphoric acid (H3PO4). Activated carbon aerogel bearing sulfonic acid (ACA-SO3H), Cs2.5H0.5PW12O40-impregnated activated carbon aerogel (Cs2.5H0.5PW12O40/ACA), and Cs2.5H0.5PW12O40-impregnated activated carbon aerogel bearing sulfonic acid (Cs2.5H0.5PW12O40/ACA-SO3H) were prepared in order to provide acid sites to ACA. Palladium catalysts were then supported on ACA, ACA-SO3H, Cs2.5H0.5PW12O40/ACA, and Cs2.5H0.5PW12O40/ACA-SO3H by an incipient wetness impregnation method. The prepared Pd/ACA, Pd/ACA-SO3H, Pd/Cs2.5H0.5PW12O40/ACA, and Pd/Cs2.5H0.5PW12O40/ACA-SO3H catalysts were applied to the decomposition of 1,3-diphenoxybenzene. 1,3-Diphenoxybenzene was used as a trimeric lignin model compound for representing C-O bond in lignin. Cyclohexanol, benzene, and phenol were mainly produced by the decomposition of 1,3-diphenoxybenzene. 4-Phenoxyphenol was also produced as an intermediate by the decomposition of 1,3-diphenoxybenzene. Conversion of 1,3-diphenoxybenzene and total yield for main products (cyclohexanol, benzene, and phenol) increased with increasing acidity of the catalysts. Among the catalysts tested, Pd/Cs2.5H0.5PW12O40/ACA-SO3H with the largest acidity showed the highest conversion of 1,3-diphenoxybenzene and total yield for main products. Pd/Cs2.5H0.5PW12O40/ACA-SO3H also served as a stable and reusable catalyst in the decomposition of 1,3-diphenoxybenzene.
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Activated carbon aerogel (ACA) was prepared by a chemical activation of carbon aerogel using phosphoric acid (H3PO4). Activated carbon aerogel bearing sulfonic acid (ACA-SO3H), Cs2.5H0.5PW12O40-impregnated activated carbon aerogel (Cs2.5H0.5PW12O40/ACA), and Cs2.5H0.5PW12O40-impregnated activated carbon aerogel bearing sulfonic acid (Cs2.5H0.5PW12O40/ACA-SO3H) were prepared in order to provide acid sites to ACA. Palladium catalysts were then supported on ACA, ACA-SO3H, Cs2.5H0.5PW12O40/ACA, and Cs2.5H0.5PW12O40/ACA-SO3H by an incipient wetness impregnation method. The prepared Pd/ACA, Pd/ACA-SO3H, Pd/Cs2.5H0.5PW12O40/ACA, and Pd/Cs2.5H0.5PW12O40/ACA-SO3H catalysts were applied to the decomposition of 1,3-diphenoxybenzene. 1,3-Diphenoxybenzene was used as a trimeric lignin model compound for representing C-O bond in lignin. Cyclohexanol, benzene, and phenol were mainly produced by the decomposition of 1,3-diphenoxybenzene. 4-Phenoxyphenol was also produced as an intermediate by the decomposition of 1,3-diphenoxybenzene. Conversion of 1,3-diphenoxybenzene and total yield for main products (cyclohexanol, benzene, and phenol) increased with increasing acidity of the catalysts. Among the catalysts tested, Pd/Cs2.5H0.5PW12O40/ACA-SO3H with the largest acidity showed the highest conversion of 1,3-diphenoxybenzene and total yield for main products. Pd/Cs2.5H0.5PW12O40/ACA-SO3H also served as a stable and reusable catalyst in the decomposition of 1,3-diphenoxybenzene.</description><identifier>ISSN: 0926-860X</identifier><identifier>EISSN: 1873-3875</identifier><identifier>DOI: 10.1016/j.apcata.2013.02.020</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>1,3-Diphenoxybenzene ; Acidic activated carbon aerogel ; Activated carbon ; Adsorbents ; Aerogels ; Bearing ; Catalysis ; Catalysts ; Chemistry ; Colloidal state and disperse state ; Decomposition ; Exact sciences and technology ; General and physical chemistry ; Heteropolyacid ; Lignin decomposition ; Palladium ; Pd catalyst ; Phenol ; Porous materials ; Surface physical chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Applied catalysis. A, General, 2013-04, Vol.456, p.59-66</ispartof><rights>2013 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-7c15e8a556da171f246a2138807cbb819102f2a6e2e67b3007b58ebb48dd3b9a3</citedby><cites>FETCH-LOGICAL-c406t-7c15e8a556da171f246a2138807cbb819102f2a6e2e67b3007b58ebb48dd3b9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.apcata.2013.02.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27292946$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Hai Woong</creatorcontrib><creatorcontrib>Kim, Jeong Kwon</creatorcontrib><creatorcontrib>Hong, Ung Gi</creatorcontrib><creatorcontrib>Lee, Yoon Jae</creatorcontrib><creatorcontrib>Choi, Jung Ho</creatorcontrib><creatorcontrib>Bang, Yongju</creatorcontrib><creatorcontrib>Song, In Kyu</creatorcontrib><title>Catalytic decomposition of 1,3-diphenoxybenzene to monomeric cyclic compounds over palladium catalysts supported on acidic activated carbon aerogels</title><title>Applied catalysis. A, General</title><description>[Display omitted] ► Pd catalysts supported on acidic ACAs (activated carbon aerogels) were prepared. ► Catalytic decomposition of 1,3-diphenoxybenzene was conducted. ► Acidity of the catalysts played an important role in the reaction. ► Total yield for monomeric cyclic compounds increased with increasing catalyst acidity. Activated carbon aerogel (ACA) was prepared by a chemical activation of carbon aerogel using phosphoric acid (H3PO4). Activated carbon aerogel bearing sulfonic acid (ACA-SO3H), Cs2.5H0.5PW12O40-impregnated activated carbon aerogel (Cs2.5H0.5PW12O40/ACA), and Cs2.5H0.5PW12O40-impregnated activated carbon aerogel bearing sulfonic acid (Cs2.5H0.5PW12O40/ACA-SO3H) were prepared in order to provide acid sites to ACA. Palladium catalysts were then supported on ACA, ACA-SO3H, Cs2.5H0.5PW12O40/ACA, and Cs2.5H0.5PW12O40/ACA-SO3H by an incipient wetness impregnation method. The prepared Pd/ACA, Pd/ACA-SO3H, Pd/Cs2.5H0.5PW12O40/ACA, and Pd/Cs2.5H0.5PW12O40/ACA-SO3H catalysts were applied to the decomposition of 1,3-diphenoxybenzene. 1,3-Diphenoxybenzene was used as a trimeric lignin model compound for representing C-O bond in lignin. Cyclohexanol, benzene, and phenol were mainly produced by the decomposition of 1,3-diphenoxybenzene. 4-Phenoxyphenol was also produced as an intermediate by the decomposition of 1,3-diphenoxybenzene. Conversion of 1,3-diphenoxybenzene and total yield for main products (cyclohexanol, benzene, and phenol) increased with increasing acidity of the catalysts. Among the catalysts tested, Pd/Cs2.5H0.5PW12O40/ACA-SO3H with the largest acidity showed the highest conversion of 1,3-diphenoxybenzene and total yield for main products. Pd/Cs2.5H0.5PW12O40/ACA-SO3H also served as a stable and reusable catalyst in the decomposition of 1,3-diphenoxybenzene.</description><subject>1,3-Diphenoxybenzene</subject><subject>Acidic activated carbon aerogel</subject><subject>Activated carbon</subject><subject>Adsorbents</subject><subject>Aerogels</subject><subject>Bearing</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Decomposition</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Heteropolyacid</subject><subject>Lignin decomposition</subject><subject>Palladium</subject><subject>Pd catalyst</subject><subject>Phenol</subject><subject>Porous materials</subject><subject>Surface physical chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0926-860X</issn><issn>1873-3875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kc2q1EAQhYMoOF59Axe9EVyYsbqTdJKNIMP1By64UXDXVKor2kOSjt09g-Nz-MB2nItLoaCgON-pKk5RPJewlyD16-MeV8KEewWy2oPKBQ-Knezaqqy6tnlY7KBXuuw0fH1cPInxCACq7ptd8fuQuemSHAnL5OfVR5ecX4QfhXxVldat33nxPy8DL794YZG8mP3iZw4ZoQtNW9u402Kj8GcOYsVpQutOs6C_5jFFEU_r6kNiK7I3krMZQ0rujNuMMAzbnIP_xlN8WjwacYr87L7fFF_e3X4-fCjvPr3_eHh7V1INOpUtyYY7bBptUbZyVLVGJauug5aGoZO9BDUq1KxYt0MF0A5Nx8NQd9ZWQ4_VTfHy6rsG_-PEMZnZReJ8_cL-FI2sdd00oJXO0voqpeBjDDyaNbgZw8VIMFsI5miuIZgtBAMqF2Tsxf0GjITTGHAhF_-xqlW96uvN_s1Vl7_ns-NgIjleiK0LTMlY7_6_6A8XkaKb</recordid><startdate>20130410</startdate><enddate>20130410</enddate><creator>Park, Hai Woong</creator><creator>Kim, Jeong Kwon</creator><creator>Hong, Ung Gi</creator><creator>Lee, Yoon Jae</creator><creator>Choi, Jung Ho</creator><creator>Bang, Yongju</creator><creator>Song, In Kyu</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130410</creationdate><title>Catalytic decomposition of 1,3-diphenoxybenzene to monomeric cyclic compounds over palladium catalysts supported on acidic activated carbon aerogels</title><author>Park, Hai Woong ; Kim, Jeong Kwon ; Hong, Ung Gi ; Lee, Yoon Jae ; Choi, Jung Ho ; Bang, Yongju ; Song, In Kyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-7c15e8a556da171f246a2138807cbb819102f2a6e2e67b3007b58ebb48dd3b9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>1,3-Diphenoxybenzene</topic><topic>Acidic activated carbon aerogel</topic><topic>Activated carbon</topic><topic>Adsorbents</topic><topic>Aerogels</topic><topic>Bearing</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Decomposition</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Heteropolyacid</topic><topic>Lignin decomposition</topic><topic>Palladium</topic><topic>Pd catalyst</topic><topic>Phenol</topic><topic>Porous materials</topic><topic>Surface physical chemistry</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Hai Woong</creatorcontrib><creatorcontrib>Kim, Jeong Kwon</creatorcontrib><creatorcontrib>Hong, Ung Gi</creatorcontrib><creatorcontrib>Lee, Yoon Jae</creatorcontrib><creatorcontrib>Choi, Jung Ho</creatorcontrib><creatorcontrib>Bang, Yongju</creatorcontrib><creatorcontrib>Song, In Kyu</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</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 catalysis. A, General</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Hai Woong</au><au>Kim, Jeong Kwon</au><au>Hong, Ung Gi</au><au>Lee, Yoon Jae</au><au>Choi, Jung Ho</au><au>Bang, Yongju</au><au>Song, In Kyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalytic decomposition of 1,3-diphenoxybenzene to monomeric cyclic compounds over palladium catalysts supported on acidic activated carbon aerogels</atitle><jtitle>Applied catalysis. A, General</jtitle><date>2013-04-10</date><risdate>2013</risdate><volume>456</volume><spage>59</spage><epage>66</epage><pages>59-66</pages><issn>0926-860X</issn><eissn>1873-3875</eissn><abstract>[Display omitted] ► Pd catalysts supported on acidic ACAs (activated carbon aerogels) were prepared. ► Catalytic decomposition of 1,3-diphenoxybenzene was conducted. ► Acidity of the catalysts played an important role in the reaction. ► Total yield for monomeric cyclic compounds increased with increasing catalyst acidity. Activated carbon aerogel (ACA) was prepared by a chemical activation of carbon aerogel using phosphoric acid (H3PO4). Activated carbon aerogel bearing sulfonic acid (ACA-SO3H), Cs2.5H0.5PW12O40-impregnated activated carbon aerogel (Cs2.5H0.5PW12O40/ACA), and Cs2.5H0.5PW12O40-impregnated activated carbon aerogel bearing sulfonic acid (Cs2.5H0.5PW12O40/ACA-SO3H) were prepared in order to provide acid sites to ACA. Palladium catalysts were then supported on ACA, ACA-SO3H, Cs2.5H0.5PW12O40/ACA, and Cs2.5H0.5PW12O40/ACA-SO3H by an incipient wetness impregnation method. The prepared Pd/ACA, Pd/ACA-SO3H, Pd/Cs2.5H0.5PW12O40/ACA, and Pd/Cs2.5H0.5PW12O40/ACA-SO3H catalysts were applied to the decomposition of 1,3-diphenoxybenzene. 1,3-Diphenoxybenzene was used as a trimeric lignin model compound for representing C-O bond in lignin. Cyclohexanol, benzene, and phenol were mainly produced by the decomposition of 1,3-diphenoxybenzene. 4-Phenoxyphenol was also produced as an intermediate by the decomposition of 1,3-diphenoxybenzene. Conversion of 1,3-diphenoxybenzene and total yield for main products (cyclohexanol, benzene, and phenol) increased with increasing acidity of the catalysts. Among the catalysts tested, Pd/Cs2.5H0.5PW12O40/ACA-SO3H with the largest acidity showed the highest conversion of 1,3-diphenoxybenzene and total yield for main products. Pd/Cs2.5H0.5PW12O40/ACA-SO3H also served as a stable and reusable catalyst in the decomposition of 1,3-diphenoxybenzene.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcata.2013.02.020</doi><tpages>8</tpages></addata></record>
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subjects 1,3-Diphenoxybenzene
Acidic activated carbon aerogel
Activated carbon
Adsorbents
Aerogels
Bearing
Catalysis
Catalysts
Chemistry
Colloidal state and disperse state
Decomposition
Exact sciences and technology
General and physical chemistry
Heteropolyacid
Lignin decomposition
Palladium
Pd catalyst
Phenol
Porous materials
Surface physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Catalytic decomposition of 1,3-diphenoxybenzene to monomeric cyclic compounds over palladium catalysts supported on acidic activated carbon aerogels
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