首页> 外文期刊>International Journal of Greenhouse Gas Control >Amine degradation in CO2 capture. 2. New degradation products of MEA. Pyrazine and alkylpyrazines: Analysis, mechanism of formation and toxicity
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Amine degradation in CO2 capture. 2. New degradation products of MEA. Pyrazine and alkylpyrazines: Analysis, mechanism of formation and toxicity

机译:二氧化碳捕获中的胺降解。 2. MEA的新退化产品。 吡嗪和烷基吡嗪:分析,形成和毒性机制

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摘要

Amine degradation in post-combustion CO2 capture is a main problem because of its consequences on process units and the potential impact of degradation products on environment. Ethanolamine (MEA) is the benchmark amine for this application. Although MEA degradation has been intensively studied, some degradation products are still unidentified. In this article, new degradation products of MEA are reported: pyrazine and 9 alkylpyrazines. A new analytical method based on HS-SPME and GC-MS was developed to identify and quantify the 10 pyrazines present in two pilot plant samples. A mechanism for their formation was proposed. The toxicity of these molecules was assessed based on available toxicological data and, when the information was not sufficient, a computational approach was used: TOPKAT and DEREK SARs. LD50, skin and eye irritancy potential, genotoxicity and reproductive effects were assessed. The study showed that the ten identified pyrazines are currently not indicating toxicological concern at the level of intake estimated at 0.2-120 mu g/day in Europe
机译:燃烧后二氧化碳捕获中的胺降解是主要问题,因为它对过程单位的后果和降解产品对环境的潜在影响。乙醇胺(MEA)是该应用的基准胺。虽然MEA降解已经集中研究,但一些降解产物仍未认定。在本文中,报告了MEA的新退化产物:吡嗪和9个烷基吡嗪。开发了一种基于HS-SPME和GC-MS的新分析方法,以识别和量化两种试验厂样品中存在的10个吡嗪。提出了一种形成它们的机制。基于可用的毒理数据评估这些分子的毒性,并且当信息不足时,使用了计算方法:Topkat和Derek SARS。 LD50,皮肤和眼睛刺激性潜力,遗传毒性和生殖效应被评估。该研究表明,十个鉴定的吡嗪目前没有表明在欧洲0.2-120μg/天的摄入量下的毒理学关注

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