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        <identifier>oai:hiroshima.repo.nii.ac.jp:02006139</identifier>
        <datestamp>2025-02-21T06:41:42Z</datestamp>
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          <dc:title>Microwave-Assisted Synthesis of C/SiO2 Composite with Controllable Silica Nanoparticle Size</dc:title>
          <dc:creator>Arif, Aditya F.</dc:creator>
          <dc:creator>Taniguchi, Shuto</dc:creator>
          <dc:creator>Izawa, Takafumi</dc:creator>
          <dc:creator>Kamikubo, Kazuki</dc:creator>
          <dc:creator>Iwasaki, Hideharu</dc:creator>
          <dc:creator>Ogi, Takasi</dc:creator>
          <dc:description>AC/SiO composite was produced from 3-aminophenol and tetraethyl orthosilicate (TEOS) by a synthesis protocol that involved microwave irradiation. This protocol featured simultaneous 3-aminophenol polymerization and TEOS hydrolysis and condensation, which were achieved rapidly in a microwave reactor. The SiO2 component was formed from low-concentration TEOS conﬁned in cetyltrimethylammonium bromide micelles. We demonstrated a control of the SiO2 particle size, ranging from 20 to 90 nm, by varying the 3-aminophenol concentration. The carbon component provided a microporous structure that greatly contributed to the high speciﬁc surface area, 375 m2/g, and served as a host for the nitrogen functional groups with a content of 5.34%, 74% of which were pyridinic type. The composite formation mechanism was clariﬁed from time-series scanning electron microscopy images and dynamic light scattering analysis. An understanding of the composite formation mechanism in this protocol will enable the design of composite morphologies for speciﬁc applications.</dc:description>
          <dc:description>This work was supported by JSPS KAKENHI Grant Numbers 26709061 and 16K13642 and was partly supported by the Center for Functional Nano Oxides at Hiroshima University.</dc:description>
          <dc:description>http://purl.org/coar/resource_type/c_6501</dc:description>
          <dc:publisher>American Chemical Society</dc:publisher>
          <dc:date>2018-04-11</dc:date>
          <dc:type>VoR</dc:type>
          <dc:identifier>2470-1343</dc:identifier>
          <dc:identifier>4063</dc:identifier>
          <dc:identifier>ACS Omega</dc:identifier>
          <dc:identifier>4</dc:identifier>
          <dc:identifier>3</dc:identifier>
          <dc:identifier>4069</dc:identifier>
          <dc:identifier>4063</dc:identifier>
          <dc:identifier>ACS Omega</dc:identifier>
          <dc:identifier>https://hiroshima.repo.nii.ac.jp/records/2006139</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>10.1021/acsomega.8b00340</dc:relation>
          <dc:relation>https://pubs.acs.org/doi/full/10.1021/acsomega.8b00340</dc:relation>
          <dc:rights>open access</dc:rights>
          <dc:rights>© 2018 American Chemical Society, This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.</dc:rights>
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