Ni-doped mesoporous carbon obtained from hydrothermal carbonization of cellulose and their catalytic hydrogenation activity study
Ni-doped spherical mesoporous carbon catalysts (Ni/C n ) were prepared via one-pot hydrothermal carbonization of microcrystalline cellulose (MCC) with nickel acetate as the Ni source. This exhibited a high conversion rate for p -nitrophenol (PNP) hydrogenation to p -aminophenol (PAP). The obtained c...
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creator | Wu, Qiong Liu, Shiwei Xie, Congxia Yu, Hailong Liu, Yue Yu, Shitao Huang, Lang |
description | Ni-doped spherical mesoporous carbon catalysts (Ni/C
n
) were prepared via one-pot hydrothermal carbonization of microcrystalline cellulose (MCC) with nickel acetate as the Ni source. This exhibited a high conversion rate for
p
-nitrophenol (PNP) hydrogenation to
p
-aminophenol (PAP). The obtained catalysts contained 0.87–6.84 wt% nickel content that primarily consisted of metallic nickel, with a small amount of nickel oxide. The Ni additive could be beneficial in the formation of the mesoporous structure. The results showed that as the Ni content increased, the mesoporous percentage increased. The doped Ni was monodispersed particles added into the carbon skeleton with an average particle size of 23.6 nm. They were surrounded by ordered striped carbon that exhibited a graphite-like structure. The catalytic hydrogenation reaction took place at normal temperatures and pressure exhibited high catalytic activity. The degradation rate of PNP reached 99.7% when 0.30 g of the Ni/C
0.2
-900 catalysts was used for a reaction time of 40 min, with corresponding apparent rates constant of 1.68 × 10
−3
S
−1
, apparent activation energy of only 43.25 kJ/mol. |
doi_str_mv | 10.1007/s10853-018-2054-5 |
format | Article |
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n
) were prepared via one-pot hydrothermal carbonization of microcrystalline cellulose (MCC) with nickel acetate as the Ni source. This exhibited a high conversion rate for
p
-nitrophenol (PNP) hydrogenation to
p
-aminophenol (PAP). The obtained catalysts contained 0.87–6.84 wt% nickel content that primarily consisted of metallic nickel, with a small amount of nickel oxide. The Ni additive could be beneficial in the formation of the mesoporous structure. The results showed that as the Ni content increased, the mesoporous percentage increased. The doped Ni was monodispersed particles added into the carbon skeleton with an average particle size of 23.6 nm. They were surrounded by ordered striped carbon that exhibited a graphite-like structure. The catalytic hydrogenation reaction took place at normal temperatures and pressure exhibited high catalytic activity. The degradation rate of PNP reached 99.7% when 0.30 g of the Ni/C
0.2
-900 catalysts was used for a reaction time of 40 min, with corresponding apparent rates constant of 1.68 × 10
−3
S
−1
, apparent activation energy of only 43.25 kJ/mol.</description><identifier>ISSN: 0022-2461</identifier><identifier>EISSN: 1573-4803</identifier><identifier>DOI: 10.1007/s10853-018-2054-5</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Activation energy ; Aminophenol ; Carbon ; Carbonization ; Catalysis ; Catalysts ; Catalytic activity ; Cellulose ; Cellulose acetate ; Characterization and Evaluation of Materials ; Chemistry and Materials Science ; Classical Mechanics ; Crystalline cellulose ; Crystallography and Scattering Methods ; Hydrogenation ; Materials Science ; Nickel ; Nitrophenol ; Polymer Sciences ; Polymers ; Reaction time ; Solid Mechanics</subject><ispartof>Journal of materials science, 2018-05, Vol.53 (10), p.7900-7910</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Journal of Materials Science is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-9fc33cf2793267079efbed5a40a51a2a77f18a8af262dfee83f10997743f76ee3</citedby><cites>FETCH-LOGICAL-c426t-9fc33cf2793267079efbed5a40a51a2a77f18a8af262dfee83f10997743f76ee3</cites><orcidid>0000-0002-9434-8133</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10853-018-2054-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10853-018-2054-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Wu, Qiong</creatorcontrib><creatorcontrib>Liu, Shiwei</creatorcontrib><creatorcontrib>Xie, Congxia</creatorcontrib><creatorcontrib>Yu, Hailong</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>Yu, Shitao</creatorcontrib><creatorcontrib>Huang, Lang</creatorcontrib><title>Ni-doped mesoporous carbon obtained from hydrothermal carbonization of cellulose and their catalytic hydrogenation activity study</title><title>Journal of materials science</title><addtitle>J Mater Sci</addtitle><description>Ni-doped spherical mesoporous carbon catalysts (Ni/C
n
) were prepared via one-pot hydrothermal carbonization of microcrystalline cellulose (MCC) with nickel acetate as the Ni source. This exhibited a high conversion rate for
p
-nitrophenol (PNP) hydrogenation to
p
-aminophenol (PAP). The obtained catalysts contained 0.87–6.84 wt% nickel content that primarily consisted of metallic nickel, with a small amount of nickel oxide. The Ni additive could be beneficial in the formation of the mesoporous structure. The results showed that as the Ni content increased, the mesoporous percentage increased. The doped Ni was monodispersed particles added into the carbon skeleton with an average particle size of 23.6 nm. They were surrounded by ordered striped carbon that exhibited a graphite-like structure. The catalytic hydrogenation reaction took place at normal temperatures and pressure exhibited high catalytic activity. The degradation rate of PNP reached 99.7% when 0.30 g of the Ni/C
0.2
-900 catalysts was used for a reaction time of 40 min, with corresponding apparent rates constant of 1.68 × 10
−3
S
−1
, apparent activation energy of only 43.25 kJ/mol.</description><subject>Activation energy</subject><subject>Aminophenol</subject><subject>Carbon</subject><subject>Carbonization</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Cellulose</subject><subject>Cellulose acetate</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry and Materials Science</subject><subject>Classical Mechanics</subject><subject>Crystalline cellulose</subject><subject>Crystallography and Scattering Methods</subject><subject>Hydrogenation</subject><subject>Materials Science</subject><subject>Nickel</subject><subject>Nitrophenol</subject><subject>Polymer Sciences</subject><subject>Polymers</subject><subject>Reaction time</subject><subject>Solid Mechanics</subject><issn>0022-2461</issn><issn>1573-4803</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp10U2L1TAUBuAiCl5Hf4C7gisXGU-SpmmXw6DjwDCCH-twbnpyJ0PbXJNUpu785-bSAZmFZBFInjcn8FbVWw7nHEB_SBw6JRnwjglQDVPPqh1XWrKmA_m82gEIwUTT8pfVq5TuAUBpwXfVn1vPhnCkoZ4ohWOIYUm1xbgPcx32Gf1crlwMU323DjHkO4oTjo_C_8bsT9DVlsZxGUOiGuehLszHgjKOa_Z2yx5o3jja7H_5vNYpL8P6unrhcEz05nE_q358-vj98jO7-XJ1fXlxw2wj2sx6Z6W0TuheilaD7sntaVDYACqOArV2vMMOnWjF4Ig66Tj0vdaNdLolkmfVu-3dYww_F0rZ3IclzmWkEUL1LZcSZFHnmzrgSMbPLuSItqyBJm_DTM6X8wsleuhl2_ESeP8kUEymh3zAJSVz_e3rU8s3a2NIKZIzx-gnjKvhYE41mq1GU2o0pxqNKhmxZVKx84Hiv2__P_QX_aWiEg</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Wu, Qiong</creator><creator>Liu, Shiwei</creator><creator>Xie, Congxia</creator><creator>Yu, Hailong</creator><creator>Liu, Yue</creator><creator>Yu, Shitao</creator><creator>Huang, Lang</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L6V</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><orcidid>https://orcid.org/0000-0002-9434-8133</orcidid></search><sort><creationdate>20180501</creationdate><title>Ni-doped mesoporous carbon obtained from hydrothermal carbonization of cellulose and their catalytic hydrogenation activity study</title><author>Wu, Qiong ; Liu, Shiwei ; Xie, Congxia ; Yu, Hailong ; Liu, Yue ; Yu, Shitao ; Huang, Lang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-9fc33cf2793267079efbed5a40a51a2a77f18a8af262dfee83f10997743f76ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Activation energy</topic><topic>Aminophenol</topic><topic>Carbon</topic><topic>Carbonization</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Cellulose</topic><topic>Cellulose acetate</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry and Materials Science</topic><topic>Classical Mechanics</topic><topic>Crystalline cellulose</topic><topic>Crystallography and Scattering Methods</topic><topic>Hydrogenation</topic><topic>Materials Science</topic><topic>Nickel</topic><topic>Nitrophenol</topic><topic>Polymer Sciences</topic><topic>Polymers</topic><topic>Reaction time</topic><topic>Solid Mechanics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Qiong</creatorcontrib><creatorcontrib>Liu, Shiwei</creatorcontrib><creatorcontrib>Xie, Congxia</creatorcontrib><creatorcontrib>Yu, Hailong</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>Yu, Shitao</creatorcontrib><creatorcontrib>Huang, Lang</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>ProQuest Engineering Collection</collection><collection>Engineering Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><jtitle>Journal of materials science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Qiong</au><au>Liu, Shiwei</au><au>Xie, Congxia</au><au>Yu, Hailong</au><au>Liu, Yue</au><au>Yu, Shitao</au><au>Huang, Lang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ni-doped mesoporous carbon obtained from hydrothermal carbonization of cellulose and their catalytic hydrogenation activity study</atitle><jtitle>Journal of materials science</jtitle><stitle>J Mater Sci</stitle><date>2018-05-01</date><risdate>2018</risdate><volume>53</volume><issue>10</issue><spage>7900</spage><epage>7910</epage><pages>7900-7910</pages><issn>0022-2461</issn><eissn>1573-4803</eissn><abstract>Ni-doped spherical mesoporous carbon catalysts (Ni/C
n
) were prepared via one-pot hydrothermal carbonization of microcrystalline cellulose (MCC) with nickel acetate as the Ni source. This exhibited a high conversion rate for
p
-nitrophenol (PNP) hydrogenation to
p
-aminophenol (PAP). The obtained catalysts contained 0.87–6.84 wt% nickel content that primarily consisted of metallic nickel, with a small amount of nickel oxide. The Ni additive could be beneficial in the formation of the mesoporous structure. The results showed that as the Ni content increased, the mesoporous percentage increased. The doped Ni was monodispersed particles added into the carbon skeleton with an average particle size of 23.6 nm. They were surrounded by ordered striped carbon that exhibited a graphite-like structure. The catalytic hydrogenation reaction took place at normal temperatures and pressure exhibited high catalytic activity. The degradation rate of PNP reached 99.7% when 0.30 g of the Ni/C
0.2
-900 catalysts was used for a reaction time of 40 min, with corresponding apparent rates constant of 1.68 × 10
−3
S
−1
, apparent activation energy of only 43.25 kJ/mol.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10853-018-2054-5</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9434-8133</orcidid></addata></record> |
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subjects | Activation energy Aminophenol Carbon Carbonization Catalysis Catalysts Catalytic activity Cellulose Cellulose acetate Characterization and Evaluation of Materials Chemistry and Materials Science Classical Mechanics Crystalline cellulose Crystallography and Scattering Methods Hydrogenation Materials Science Nickel Nitrophenol Polymer Sciences Polymers Reaction time Solid Mechanics |
title | Ni-doped mesoporous carbon obtained from hydrothermal carbonization of cellulose and their catalytic hydrogenation activity study |
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