Institutional Repository of Dalian Institute of Chemical Physics, CAS
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    Cancer Research UK (CRUK)[C37/A18784]

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    [DICP DMTO201306]

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    Ministry of Science and Technology[2016YFA0200700]

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    National Natural Science Foundation of China[21473173]

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    Youth Innovation Promotion Association of Chinese Academy of Sciences[2018214]

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    Global Expert program funding of China

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    Natural Science Foundation of Shanxi Province[201701D121017]

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    CO2 capture and adsorption kinetic study of amine-modified MIL-101 (Cr)

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    MIL-101 (Cr) was synthesized by a hydrothermal method and used as support to prepare a series of polyethylenimine (PEI) incorporated MIL-101 (Cr) by wet impregnation method. All characterization results revealed that the structure of MIL-101 (Cr) was well-maintained by the incorporation of polyethylenimine and confirmed the presence of PEI within MIL-101 (Cr). The CO2 adsorption studies were carried out in a fixed bed reactor from 30 to 90 degrees C, 1 bar. The adsorption of CO2 has been increased by the incorporation of PEI. It was due to the chemical interaction between the -NH2 and CO2 groups to form a carbamate. The high CO2 adsorption capacity 3.81 mmol g(-1) was shown by 70 wt% PEI loaded MIL-101(Cr) at 75 degrees C,1 bar, because of more number of NH2 groups and a high number of CO2 molecules diffusion. Its adsorption capacity was 4.7 times higher than the adsorption capacity of MIL-101 (Cr) (0.80 mmol g(-1)). Moreover, in moisture condition, CO2 adsorption capacity was increased to 4.4 mmol g(-1) by the formation of ammonium bicarbonate and showed good adsorption stability throughout each adsorption-desorption cycle. The Avrami adsorption kinetic model was well fitted with experimental breakthrough CO2 adsorption data of MIL-101 (Cr)-PEI-70. It suggested that the adsorption of CO2 on PEI incorporated material was chemical adsorption. (C) 2019 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved

    Natural Science Basic Research Plan in Shaanxi Province of China[2018JM2048]

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