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Carbon Dioxide Capture by an Amine Functionalized Ionic Liquid: Fundamental Differences of Surface and Bulk Behavior

机译:胺功能化离子液体捕获的二氧化碳:表面和本体行为的根本差异

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摘要

Carbon dioxide (CO_2) absorption by the amine-functionalized ionic liquid (IL) dihydroxyethyl dimethylammonium taurinate at 310 K was studied using surface- and bulk-sensitive experimental techniques. From near-ambient pressure X-ray photoelectron spectroscopy at 0.9 mbar CO_2, the amount of captured CO_2 per mole of IL in the near-surface region is quantified to ~0.58 mol, with ~0.15 mol in form of carbamate dianions and ~0.43 mol in form of carbamic acid. From isothermal uptake experiments combined with infrared spectroscopy, CO_2 is found to be bound in the bulk as carbamate (with nominally 0.5 mol of CO_2 bound per 1 mol of IL) up to ~2.5 bar CO_2, and as carbamic acid (with nominally 1 mol CO_2 bound per 1 mol IL) at higher pressures. We attribute the fact that at low pressures carbamic acid is the dominating species in the near-surface region, while only carbamate is formed in the bulk, to differences in solvation in the outermost IL layers as compared to the bulk situation.
机译:使用表面敏感和本体敏感的实验技术研究了氨基官能化离子液体(IL)牛磺酸二羟乙基二甲基铵牛磺酸对二氧化碳(CO_2)的吸收。从0.9 mbar CO_2的近环境压力X射线光电子能谱分析,近表面区域中每摩尔IL的捕获CO_2量被量化为〜0.58 mol,其中氨基甲酸酯为〜0.15 mol,约为0.43 mol。以氨基甲酸的形式通过等温吸收实验与红外光谱结合,发现CO_2以氨基甲酸酯(每1 mol IL名义上结合有0.5 mol CO_2)和高达2.5 bar CO_2的氨基甲酸酯(名义上为1 mol)结合。在较高压力下,每1摩尔IL)结合的CO_2。我们认为,在低压下,氨基甲酸是近表面区域的主要物质,而在本体中仅形成氨基甲酸酯,这是由于与本体情况相比,最外层IL层的溶剂化程度不同。

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  • 来源
    《Journal of the American Chemical Society》 |2014年第1期|436-441|共6页
  • 作者单位

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Chemische Reaktionstechnik, Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Chemische Reaktionstechnik, Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Chemische Reaktionstechnik, Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Chemische Reaktionstechnik, Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

    Lehrstuhl fuer Physikalische Chemie Ⅱ , Universitaet Erlangen-Nuernberg, Egerlandstrasse 3, 91058 Erlangen, Germany;

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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:11:00

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