کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
42630 45934 2008 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Noble-metal-containing nanoporous carbon synthesized within the interlayer space of montmorillonite and its catalytic property
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Noble-metal-containing nanoporous carbon synthesized within the interlayer space of montmorillonite and its catalytic property
چکیده انگلیسی

We synthesized nanoporous carbon containing noble metal particles via the co-intercalation of noble metal precursors and sucrose into montmorillonite (mont) and the subsequent sulfuric acid-catalyzed carbonization. A TEM image of the Ru-containing porous carbon material (Ru-C/mont) showed Ru particles of uniform particle sizes (1–2 nm). Residual sulfur species were also observed in Ru-C/mont even after heating in N2 flow at 1073 K. The FT-IR spectra of Ru-C/mont showed peaks corresponding to the asymmetric SO stretching mode of SO3− as well as to the asymmetric and symmetric stretching modes of SiOAl. SO3− and SiOAl acted as acid sites. The catalytic activity of Ru-C/mont in cyclopentene hydration was investigated. Cyclopentene hydration proceeded using C/mont as catalyst even without Ru incorporation. However, the catalytic activity of the synthesized carbon material increased in the presence of Ru. The cyclopentanol yield was higher using Ru-C/mont than using H-ZSM-5 or Nb2O5·nH2O as a catalyst. Thus, the coexistence of acid sites and Ru plays a key role in cyclopentanol formation.

We synthesized Ru-containing porous carbon materials (Ru-C/mont) of uniform particle sizes (1–2 nm). Ru-C/mont had a higher catalytic activity than those of the other typical solid-acid catalysts examined. The coexistence of acid sites based on SO3− and Ru plays a key role in the selective formation of cyclopentanol. Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 351, Issue 1, 15 December 2008, Pages 68–74
نویسندگان
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