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Influence of Amine Structural Characteristics on N-Nitrosamine Formation Potential Relevant to Postcombustion CO_2 Capture Systems

机译:胺结构特征对与燃烧后CO_2捕集系统相关的N-亚硝胺形成潜能的影响

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摘要

Concerns have arisen for the possible contamination of air or drinking water supplies downwind of amine-based CO_2 capture facilities by potentially carcinogenic N-nitrosamines formed from reactions between flue gas NO_x and amine solvents. This study evaluated the influence of amine structure on the potential to form total N-nitrosamines within the absorber and washwater units of a laboratory-scale CO_2 capture reactor, and in the solvent after a pressure-cooker treatment as a mimic of desorber conditions. Among 16 amines representing 3 amine classes (alkanolamines, straight-chain and cyclic diamines, and amino acids), the order of the amine was the primary determinant of total N-nitrosamine formation in the absorber unit, with total N-nitrosamine formation in the order: secondary amines ≈ tertiary amines >> primary amines. Similar results were observed upon pressure-cooker treatment, due to reactions between nitrite and amines at high temperature. For secondary and tertiary amines, total N-nitrosamine formation under these desorber-like conditions appeared to be more important than in the absorber, but for primary amines, significant formation of total N-nitrosamines was only observed in the absorber. For diamines and amino acids, total N-nitrosamine accumulation rates in washwaters were lowest for primary amines. For alkanolamines, however, total N-nitrosamine accumulation in the washwater was similar regardless of alkanolamine order, due to the combined effects of amine reactivity toward nitrosation and amine volatility. While total N-nitrosamine accumulation rates in washwaters were generally 1-2 orders of magnitude lower than in the absorber, they were comparable to absorber rates for several primary amines. Decarboxylation of the amino acid sarcosine resulted in the accumulation of significant concentrations of N-nitrosodimethyl-amine and N-nitrodimethylamine in the washwater.
机译:人们担心由烟道气NO_x与胺类溶剂之间的反应形成的潜在致癌性N-亚硝胺可能会污染胺基CO_2捕集设施的空气或饮用水。这项研究评估了胺结构对在实验室规模的CO_2捕集反应器的吸收器和洗涤水单元中以及模拟脱附条件的压力蒸煮器处理后的溶剂中形成总N-亚硝胺潜力的影响。在代表3种胺类的16种胺(链烷醇胺,直链和环状二胺和氨基酸)中,胺的顺序是吸收器单元中总N-亚硝胺形成的主要决定因素,而在吸收器单元中总N-亚硝胺的形成是顺序:仲胺≈叔胺>>伯胺。由于高温下亚硝酸盐与胺之间的反应,在压力蒸煮器处理中观察到了相似的结果。对于仲胺和叔胺,在这些类似解吸器的条件下形成的总N-亚硝胺似乎比在吸收塔中更为重要,但是对于伯胺,仅在吸收塔中观察到了明显的总N-亚硝胺形成。对于二胺和氨基酸,伯胺在洗涤水中的总N-亚硝胺累积速率最低。然而,对于烷醇胺,由于胺对亚硝化反应的反应性和胺挥发性的综合作用,洗涤水中的总N-亚硝胺累积量与烷醇胺的顺序无关。虽然洗涤水中的总N-亚硝胺累积速率通常比吸收塔低1-2个数量级,但它们与几种伯胺的吸收速率相当。氨基酸肌氨酸的脱羧作用导致洗涤水中大量浓度的N-亚硝基二甲基胺和N-硝基二甲基胺积累。

著录项

  • 来源
    《Environmental Science & Technology》 |2013年第22期|13175-13183|共9页
  • 作者

    Ning Dai; William A. Mitch;

  • 作者单位

    Department of Chemical and Environmental Engineering, Yale University, New Haven, Connecticut 06520, United States;

    Department of Civil and Environmental Engineering, Stanford University, Stanford, California 94305-4020, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 14:02:15

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