2026-03-05T16:36:57Z https://kumadai.repo.nii.ac.jp/oai

oai:kumadai.repo.nii.ac.jp:00021800 2023-06-19T19:06:18Z 426:428

Catalytic NO-H2-O2 reaction over Pt/Mg-Al-O prepared from PtCl62-- and Pt(NO2)42--exchanged hydrotalcites 濱田, 心 池上, 啓太 町田, 正人 Hamada, Shin Ikeue, Keita Machida, Masato © 2006 Elsevier B.V. All rights reserved. 431 NO-H2-O2 reaction Platinum Ion exchange Hydrotalcite application/pdf 論文(Article) 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 (>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. http://www.elsevier.com/wps/find/journaldescription.cws_home/523066/description#description Elsevier B.V. 2007-02-08 eng journal article AM http://hdl.handle.net/2298/9790 https://kumadai.repo.nii.ac.jp/records/21800 10.1016/j.apcatb.2006.08.004 http://hdl.handle.net/2298/9788 09263373 AA1082551X Applied Catalysis B: Environmental 71 1-2 1 6 https://kumadai.repo.nii.ac.jp/record/21800/files/ApCB_071-001.pdf application/pdf 1.1 MB 2020-03-02