Molecular Recognitive Photocatalysis Driven by the Selective Adsorption on Layered Titanates.

The composition of layered alkali titanates (MTiLiO M = K, Li, Na was tuned to control the swelling of the titanates in water and subsequently achieve molecular-sieve-like molecular recognitive photocatalytic decomposition of aqueous organic compounds on the titanates. Layered potassium lithium tita...

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Publicado en:Journal of the American Chemical Society Vol. 132; no. 10; pp. 3601 - 3605
Autores principales: Ide, Yusuke, Nakasato, Yuri, Ogawa, Makoto
Formato: Artículo
Publicado: American Chemical Society 3/17/2010
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Acceso en línea:Ver este registro en EBSCOhost
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      dt: 3/17/2010
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      pub: American Chemical Society
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        10.1021/ja910591v
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        atl: Molecular Recognitive Photocatalysis Driven by the Selective Adsorption on Layered Titanates.
      aug:
        au:
          Ide, Yusuke
          Nakasato, Yuri
          Ogawa, Makoto
        affil: Department of Earth Sciences, Waseda University, 1-6-1 Nishiwaseda, Shinjyuku-ku, Tokyo 169-8050, Japan
      su:
        Titanates
        Photocatalysis
        Adsorption (Chemistry)
        Organic compounds
        X-ray diffraction
        Potassium
        Hydration
      sug:
        subj:
          Titanates
          Photocatalysis
          Adsorption (Chemistry)
          Organic compounds
          X-ray diffraction
          Potassium
          Hydration
      ab: The composition of layered alkali titanates (MTiLiO M = K, Li, Na was tuned to control the swelling of the titanates in water and subsequently achieve molecular-sieve-like molecular recognitive photocatalytic decomposition of aqueous organic compounds on the titanates. Layered potassium lithium titanates with different layer charge density, KTiLiO (x = 0.61, 0.67, and 0.74), was first synthesized and then the interlayer K~ was quantitatively exchanged with Li- and Na to form LiTiLiO (x = 0.61, 0.67, and 0.76) and NaTiLiO (x = 0.61, 0.67, and 0.76). The water adsorption! desorption isotherms and X-ray diffraction patterns of the titanates revealed that the pristine K-type titanates hardly hydrated, while the Li- and Na-exchanged titanates expanded the interlayer space upon the hydration and the degree in the hydration was larger for the Na forms than for the Li ones and depended on the layer charge density. The present titanates were found to selectively adsorb benzene from an aqueous mixture of benzene, phenol, and 4-butylphenol and subsequently decompose benzene upon UV irradiation. The efficiency of the molecular recognitive photocatalytic benzene decomposition was related to the degree in the swelling of the titanates in water.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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