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        <identifier>oai:kumadai.repo.nii.ac.jp:00021800</identifier>
        <datestamp>2023-06-19T19:06:18Z</datestamp>
        <setSpec>426:428</setSpec>
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          <dc:title>Catalytic NO-H2-O2 reaction over Pt/Mg-Al-O prepared from PtCl62-- and Pt(NO2)42--exchanged hydrotalcites</dc:title>
          <dc:creator>濱田, 心</dc:creator>
          <dc:creator>94388</dc:creator>
          <dc:creator>池上, 啓太</dc:creator>
          <dc:creator>94389</dc:creator>
          <dc:creator>町田, 正人</dc:creator>
          <dc:creator>94390</dc:creator>
          <dc:creator>Hamada, Shin</dc:creator>
          <dc:creator>94382</dc:creator>
          <dc:creator>Ikeue, Keita</dc:creator>
          <dc:creator>94383</dc:creator>
          <dc:creator>Machida, Masato</dc:creator>
          <dc:creator>94384</dc:creator>
          <dc:subject>431</dc:subject>
          <dc:subject>NO-H2-O2 reaction</dc:subject>
          <dc:subject>Platinum</dc:subject>
          <dc:subject>Ion exchange</dc:subject>
          <dc:subject>Hydrotalcite</dc:subject>
          <dc:description>application/pdf</dc:description>
          <dc:description>論文(Article)</dc:description>
          <dc:description>The catalytic NO–H2–O2 reaction at low temperatures (50–130 °C) has been investigated over Pt-supported Mg–Al binary oxides, which were prepared from PtCl62− and Pt(NO2)42−–exchanged hydrotalcite(HT)-like compounds by heating at 600 °C in H2. Although the NOx conversion of both catalysts was similarly high (&gt;80%) at around 70 °C, the Pt(NO2)42−–HT catalyst exhibited the higher selectivity to N2 (53% N2 and 47% N2O), compared to 12% N2 and 88% N2O for the PtCl62−–HT catalyst. The XANES/EXAFS spectroscopy showed that Pt prepared from PtCl62−–HT is partly oxidized due to the coordination of residual chlorides, whereas Pt(NO2)42−–HT yielded highly dispersed metallic Pt. Because of the presence of chloride strongly bound to Pt, the oxidative NO adsorption as NO2/NO3 was inhibited for PtCl62−–HT. The improved N2 selectivity with an increase of oxidative NO adsorption is in accord with the catalytic property of Na–Pt/ZSM-5 in our previous work [M. Machida, T. Watanabe, Appl. Catal. B: Environ. 52 (2004) 281.], suggesting that the N2 would be formed via NO2/NO3 intermediates.</dc:description>
          <dc:description>http://www.elsevier.com/wps/find/journaldescription.cws_home/523066/description#description</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>Elsevier B.V.</dc:publisher>
          <dc:date>2007-02-08</dc:date>
          <dc:type>AM</dc:type>
          <dc:format>application/pdf</dc:format>
          <dc:identifier>Applied Catalysis B: Environmental</dc:identifier>
          <dc:identifier>1-2</dc:identifier>
          <dc:identifier>71</dc:identifier>
          <dc:identifier>1</dc:identifier>
          <dc:identifier>6</dc:identifier>
          <dc:identifier>09263373</dc:identifier>
          <dc:identifier>AA1082551X</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/record/21800/files/ApCB_071-001.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2298/9790</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/records/21800</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>http://hdl.handle.net/2298/9788</dc:relation>
          <dc:rights>© 2006 Elsevier B.V. All rights reserved.</dc:rights>
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