Amine double-functionalized adsorbents were fabricated using silica gel as supports and their capabilities for CO2 capture were examined. Aminopropyltrimethoxysilane (1N-APS), and N-1-(3-trimethoxysilylpropyl)diethylenetriamine (3N-APS) were used as grafted amine compounds, and tetraethylenepentamine and polyethyleneimine were used as impregnated species. The influence of double-functionalization method on the CO2 adsorption performance and textural properties of adsorbents was investigated. The adsorption capacity, the amine efficiency, and the thermal stability of double-functionalized sorbents depend strongly upon molecular variables associated with two different functional states (i.e., chemically grafted and physically impregnated amines). The temperature dependence of adsorption isotherms reveals that the CO2 adsorption behavior in the double-functionalized adsorbents follow the diffusion limitation model proposed by Xu et al. (Energy Fuels 16:1463-1469, 2002) where the CO2 adsorption is helped by the diffusion of impregnated amines. It is also found that the adsorption isotherm in the double-functionalized sorbent system with a proper choice for grafted and impregnated amines is nearly independent of temperature, which may offer a novel means to fabricate practically useful sorbents that can be used in a wide range of temperature without loss of CO2 adsorption capacity.
机构:
Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Calleja, G.
Sanz, R.
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Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Sanz, R.
Arencibia, A.
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Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Arencibia, A.
Sanz-Perez, E. S.
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Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
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Nara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Hanoi Univ Sci, VNU, Dept Chem Technol, Hanoi, VietnamNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Duc Sy Dao
Yamada, Hidetaka
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Res Inst Innovat Technol Earth RITE, Kyoto 6190292, JapanNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Yamada, Hidetaka
Yogo, Katsunori
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Nara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Res Inst Innovat Technol Earth RITE, Kyoto 6190292, JapanNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
机构:
Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Calleja, G.
Sanz, R.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Sanz, R.
Arencibia, A.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
Arencibia, A.
Sanz-Perez, E. S.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, SpainUniv Rey Juan Carlos, ESCET, Dept Chem & Energy Technol, Madrid 28933, Spain
机构:
Nara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Hanoi Univ Sci, VNU, Dept Chem Technol, Hanoi, VietnamNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Duc Sy Dao
Yamada, Hidetaka
论文数: 0引用数: 0
h-index: 0
机构:
Res Inst Innovat Technol Earth RITE, Kyoto 6190292, JapanNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Yamada, Hidetaka
Yogo, Katsunori
论文数: 0引用数: 0
h-index: 0
机构:
Nara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan
Res Inst Innovat Technol Earth RITE, Kyoto 6190292, JapanNara Inst Sci & Technol NAIST, Grad Sch Mat Sci, Nara 6300192, Japan