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首页> 外文期刊>International Journal of Greenhouse Gas Control >Amine neutralized amino acid as CO2 absorbents: A quantitative C-13 NMR study
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Amine neutralized amino acid as CO2 absorbents: A quantitative C-13 NMR study

机译:胺中和的氨基酸作为二氧化碳吸收剂:C-13 NMR定量研究

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摘要

Amino acids, fully or partially neutralized with amines, are a new class of CO2 absorbents that have the possibility to combine the ionic character of amino acids with the better CO2 absorbing properties of the amines to form a more energy efficient solvent with improved environmental footprint. This work studies the effect of differences in pK(a) and structural properties between the amine and amino acid on the resulting active amino group in the blend. Equimolar mixtures of the amino acids, glycine, L-alanine, L-proline, taurine and L-serine, with alkanolamines, monoethanoamine (MEA) and 2-amino-2-methyl-1-propanol (AMP), were quantitatively studied by C-13 nuclear magnetic resonance spectroscopy (NMR) at 25 degrees C. The amino acids tested in the present work were chosen based on their solubility in water and on their relative basicity (pKa) to that of the amines. It is observed that in amino acid-MEA blended systems, carbamate formation from both MEA and the amino acids occur and that generally, the amine group with highest pKa value is most favored when neutralizing the amino acid carboxylic group. If this is the amino acid an amino acid zwitterion may be formed, or, if amine has the highest pKa value, an amine-amino acid complex may be formed, rendering the amino acid amine group active toward CO2 absorption. However, the experimental data show that not only the pKa value of the amino acid is important but that also steric effects play a role in determining the preferred carbamate forming position. In the amino acid-AMP systems almost all carbamate is formed on the amino acid amine group due to the steric hindrance in AMP. Generally, addition of amine to an aqueous amino acid solution increases the amino acid solubility. In this work solid precipitation was only observed at higher CO2 loadings for L-alanine blended with both MEA and AMP. NMR spectroscopy analysis showed that the precipitate consists mainly of amino acid and bicarbonate/carbonate with very small amounts of amine
机译:氨基酸,全部或部分被胺中和,是一类新型的CO2吸收剂,它可以将氨基酸的离子特性与胺的更好的CO2吸收性能结合在一起,从而形成一种具有更高能效的溶剂,并改善环境足迹。这项工作研究了胺和氨基酸之间的pK(a)和结构特性差异对共混物中所得活性氨基的影响。氨基酸,甘氨酸,L-丙氨酸,L-脯氨酸,牛磺酸和L-丝氨酸与烷醇胺,单乙醇胺(MEA)和2-氨基-2-甲基-1-丙醇(AMP)的等摩尔混合物的定量研究如下:在25摄氏度下使用C-13核磁共振波谱(NMR)。根据氨基酸在水中的溶解度和相对于胺的相对碱性(pKa),选择本工作中测试的氨基酸。观察到在氨基酸-MEA共混体系中,由MEA和氨基酸两者形成氨基甲酸酯形成,并且通常,当中和氨基酸羧基时,最优选具有最高pKa值的胺基。如果这是氨基酸,则可以形成氨基酸两性离子,或者,如果胺具有最高的pKa值,则可以形成胺-氨基酸络合物,从而使氨基酸胺基团对CO 2吸收具有活性。然而,实验数据表明,不仅氨基酸的pKa值很重要,而且空间效应在确定优选的氨基甲酸酯形成位置中也起作用。在氨基酸-AMP系统中,由于AMP中的空间位阻,几乎所有氨基甲酸酯都在氨基酸胺基上形成。通常,将胺添加到氨基酸水溶液中会增加氨基酸溶解度。在这项工作中,仅在L-丙氨酸与MEA和AMP混合时,在较高的CO2装载量下才观察到固体沉淀。 NMR光谱分析表明沉淀物主要由氨基酸,碳酸氢盐/碳酸盐和少量胺组成

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