Carbon dioxide adsorption by zinc-functionalized ionic liquid impregnated into bio-templated mesoporous silica beads
被引:51
作者:
Arellano, Ian Harvey
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Univ S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
CSIRO Energy Flagship, Clayton, Vic 3169, AustraliaUniv S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
Arellano, Ian Harvey
[1
,2
]
Madani, S. Hadi
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机构:
Univ S Australia, Ian Wark Res Inst, Mawson Lakes, SA 5095, AustraliaUniv S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
Madani, S. Hadi
[3
]
Huang, Junhua
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CSIRO Energy Flagship, Clayton, Vic 3169, AustraliaUniv S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
Huang, Junhua
[2
]
Pendleton, Phillip
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机构:
Univ S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
Univ S Australia, Ian Wark Res Inst, Mawson Lakes, SA 5095, AustraliaUniv S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
Pendleton, Phillip
[1
,3
]
机构:
[1] Univ S Australia, Sansom Inst, Ctr Mol & Mat Sci, Adelaide, SA 5000, Australia
[2] CSIRO Energy Flagship, Clayton, Vic 3169, Australia
[3] Univ S Australia, Ian Wark Res Inst, Mawson Lakes, SA 5095, Australia
Novel high capacity hybrid sorbents for CO2 capture have been developed based on zinc-functionalized ionic liquid (IL) impregnated into mesoporous silica beads derived from calcium alginate template beads. Pore modification and development of a surface-confined layer of IL synergistically enhanced the uptake capacity (up to 8.7 wt%) and kinetics of these materials. Spectroscopic and thermophysical signatures of the IL impregnated materials confirm the existence of a highly confined IL layer at low IL:SiO2 ratio, and multilayer-mimicking bulk phase at higher IL loading. Our results clearly demonstrate that developing a thin layer of zinc-functionalized IL onto porous silica beads effectively enhances the uptake kinetics by exposing interaction sites across a large surface area, and facilitating diffusion through the pore network of the support. (C) 2015 Elsevier B.V. All rights reserved.
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
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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
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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
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