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Rhodium nanoparticles stabilized by sulfonic acid functionalized metal-organic framework for the selective hydrogenation of phenol to cyclohexanone

Ertas, Ilknur Efecan; Gulcan, Mehmet; Bulut, Ahmet; Yurderi, Mehmet; Zahmakiran, Mehmet


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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/80657</identifier>
  <creators>
    <creator>
      <creatorName>Ertas, Ilknur Efecan</creatorName>
      <givenName>Ilknur Efecan</givenName>
      <familyName>Ertas</familyName>
      <affiliation>Yuzuncu Yil Univ, Dept Chem, Nanomat &amp; Catalysis NanoMatCat Res Lab, TR-65080 Van, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Gulcan, Mehmet</creatorName>
      <givenName>Mehmet</givenName>
      <familyName>Gulcan</familyName>
      <affiliation>Yuzuncu Yil Univ, Dept Chem, Nanomat &amp; Catalysis NanoMatCat Res Lab, TR-65080 Van, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Bulut, Ahmet</creatorName>
      <givenName>Ahmet</givenName>
      <familyName>Bulut</familyName>
      <affiliation>Yuzuncu Yil Univ, Dept Chem, Nanomat &amp; Catalysis NanoMatCat Res Lab, TR-65080 Van, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yurderi, Mehmet</creatorName>
      <givenName>Mehmet</givenName>
      <familyName>Yurderi</familyName>
      <affiliation>Yuzuncu Yil Univ, Dept Chem, Nanomat &amp; Catalysis NanoMatCat Res Lab, TR-65080 Van, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Zahmakiran, Mehmet</creatorName>
      <givenName>Mehmet</givenName>
      <familyName>Zahmakiran</familyName>
      <affiliation>Yuzuncu Yil Univ, Dept Chem, Nanomat &amp; Catalysis NanoMatCat Res Lab, TR-65080 Van, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Rhodium Nanoparticles Stabilized By Sulfonic Acid Functionalized Metal-Organic Framework For The Selective Hydrogenation Of Phenol To Cyclohexanone</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2015</publicationYear>
  <dates>
    <date dateType="Issued">2015-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/80657</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.molcata.2015.09.025</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Rhodium(0) nanoparticles stabilized by sulfonic acid functionalized metal-organic framework (Rh@SMIL-101) were prepared, for the first time, by using a direct cationic exchange approach and subsequent reduction with sodium borohydride at room temperature. The characterization of the resulting Rh@SMIL-101 material was done by using multi pronged analyses including ICP-OES, EA, P-XRD, XPS, DR-UV-vis, BFFEM, HRTEM, STEM-EDX and N2-adsorption-desorption technique, which revealed that the formation of rhodium(0) nanoparticles (2.35 +/- 0.9 nm) stabilized by the framework of S-MIL-101 by keeping the host framework intact (Rh@S-MIL-101). The catalytic performance of Rh@S-MIL-101 in terms of activity, selectivity and stability was demonstrated in the hydrogenation of phenol under mild conditions (at 50 degrees C and 5 bar initial H-2 pressure). We found that Rh@S-MIL-101 catalyst selectively hydrogenated phenol to cyclohexanone with high activity (initial TOF= 78 mol cyclohexanone/mol Rh x h) and selectivity (&amp;gt;92%) at almost complete conversion (&amp;gt;95%). Moreover, the resulting rhodium nanopartides were found to be highly stable against leaching and sintering, which makes Rh@S-MIL-101 reusable heterogeneous catalyst without losing of significant activity and selectivity. (C) 2015 Elsevier B.V. All rights reserved.</description>
  </descriptions>
</resource>
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