The influence of zeolites fly ash bead/TiO2 composite material surface morphologies on their adsorption and photocatalytic performance
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作者:
Yang, Lu
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Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Univ Aberdeen, Dept Chem, Aberdeen AB24 3UE, ScotlandWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Yang, Lu
[1
,2
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Wang, Fazhou
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Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R ChinaWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Wang, Fazhou
[1
]
Hakki, Amer
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Univ Aberdeen, Dept Chem, Aberdeen AB24 3UE, ScotlandWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Hakki, Amer
[2
]
Macphee, Donald E.
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Univ Aberdeen, Dept Chem, Aberdeen AB24 3UE, ScotlandWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Macphee, Donald E.
[2
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Liu, Peng
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Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Peoples R ChinaWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Liu, Peng
[3
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Hu, Shuguang
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Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R ChinaWuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
Hu, Shuguang
[1
]
机构:
[1] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
A low cost zeolite fly ash beadiTiO(2) (ZFABT) composite materials with various surface structure features were prepared for describing those structures importance on TiO2 coating, adsorbability and photocatalytic performances. The results indicated that fly ash bead (FAB) surface was significantly altered by the precipitation/growth of secondary zeolite phases after alkali activation, which generates abundant open pores and stacked petal-liked spherical beads (similar to 2 mu m, Sodalite zeolites). More importantly, this porosity increases as activation time was increased from 2 h to 12 h, through the precipitation of sodalite and then Na-P1 (lamellar crystals) and Na-X (octahedral crystals) zeolite structures. Compared to those of unsupported TiO2 or inactivated support/TiO2 samples, all of ZFABT samples exhibited a higher adsorption capacity and photocatalytic efficiency for RhB removal. However, adsorption is not only one factor to influence TiO2 surface reaction, the intraparticle diffusion rate of rhodamine B (RhB) molecules, and light penetration are also important parameters. Alkali activated 4h ZFABT sample exhibited the highest photocatalytic activity, indicating its pore structure provided a better balance for those parameters to achieve a synergistic adsorption/photocatalytic process. The kinetics model suggested its high intraparticle diffusion rate allowed for more RhB molecules to easily reach the reaction surface, which is more important for high efficiency photocatalysis. (C) 2016 Elsevier B.V. All rights reserved.
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China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
Chen, Daimei
Zhu, Honglei
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China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
Zhu, Honglei
Wang, Xue
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China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
机构:
Hong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R China
Chen, Jun
Poon, Chi-Sun
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Hong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R China
机构:
China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
Chen, Daimei
Zhu, Honglei
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China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
Zhu, Honglei
Wang, Xue
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China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R ChinaChina Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
机构:
Hong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R China
Chen, Jun
Poon, Chi-Sun
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Hong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Civil & Struct Engn, Res Ctr Environm Technol & Management, Hong Kong, Hong Kong, Peoples R China