应用化学 ›› 2019, Vol. 36 ›› Issue (9): 1061-1068.DOI: 10.11944/j.issn.1000-0518.2019.09.190029

• 研究论文 • 上一篇    下一篇

乙醇胺类原料形成亚硝胺的比较

胡学一a,罗敏敏a,方云a*(),李俊国b,孙洋c,李华山c   

  1. a江南大学化学与材料工程学院,合成与生物胶体教育部重点实验室 江苏 无锡 214122
    b江苏清婷洗涤品有限公司 江苏 盐城 224555
    c南京华狮新材料有限公司 南京 210044
  • 收稿日期:2019-01-25 接受日期:2019-04-10 出版日期:2019-09-05 发布日期:2019-09-05
  • 通讯作者: 方云
  • 基金资助:
    国家重点研发计划(2017YFB0308904)项目资助

A Comparative Study on the Formation of Nitrosamines of Ethanolamines

HU Xueyia,LUO Minmina,FANG Yuna*(),LI Junguob,SUN Yangc,LI Huashanc   

  1. aKey Laboratory of Synthetic and Biological Colloids(Ministry of Education),School of Chemical and Material Engineering, Jiangnan University,Wuxi,Jiangsu 214122, China
    bJiangsu Qingting Washing Products Co., Ltd.,Yancheng,Jiangsu 224555,China
    cNanjing Huashi New Material Co., Ltd.,Nanjing 210044,China
  • Received:2019-01-25 Accepted:2019-04-10 Published:2019-09-05 Online:2019-09-05
  • Contact: Yun FANG
  • Supported by:
    Supported by the National Key Research and Development Plan of China(No.2017YFB0308904)

摘要:

为了探究目前表面活性剂生产和应用中用脂肪酸甲基单乙醇酰胺或脂肪酸单乙醇酰胺替代脂肪酸二乙醇酰胺的趋势的可行性,本文首先采用亚硝酸叔丁酯法合成3种乙醇胺的亚硝胺化合物作为基准物,通过鉴定产物结构研究亚硝胺的形成历程,然后以亚硝酸法合成亚硝胺化合物,通过生成率比较3种乙醇胺形成亚硝胺化合物的难易程度。 亚硝化历程分析结果表明,二乙醇胺或甲基单乙醇胺均直接形成相应的亚硝胺,而单乙醇胺通过歧化反应生成二乙醇胺继而形成少量N-亚硝基二乙醇胺。 与二乙醇胺相比,甲基单乙醇胺或单乙醇胺更不易生成亚硝胺,因此用脂肪酸甲基单乙醇酰胺或脂肪酸单乙醇酰胺替代脂肪酸二乙醇酰胺是合理可行的。 本研究结果对保障人类生命健康安全具有理论和实践意义。

关键词: 脂肪酸烷醇酰胺, 表面活性剂, 亚硝胺, 乙醇胺类, 亚硝化历程

Abstract:

To investigate the reasonability and feasibility to substitute fatty acid diethanolamide by monoethanolamide and methylethanolamide in surfactant production and application, the nitrosation of methylethanolamine or monoethanolamine was compared with diethanolamine. In this study, nitrosamines were prepared from three ethanolamines by nitrosating agents of both tert-butyl nitrite and nitrous acid. The products of nitrosation by tert-butyl nitrite were identified to reveal nitrosation mechanisms, while the yields of the nitrosamines formed by nitrous acid were used to evaluate the easiness of nitrosation among three ethanolamines. Mechanism analysis of nitrosation shows that diethanolamine or methylethanolamine forms the corresponding nitrosamines, while monoethanolamine solely forms trace amount of N-nitroso-diethanolamine owing to the formation of intermediate diethanolamine by disproportionation of monoethanolamine. The experimental results also reveal that methylethanolamine and monoethanolamine are more difficult to form nitrosamines than diethanolamine. Therefore, it is reasonable and feasible to substitute fatty acid diethanolamide by monoethanolamide and methylethanolamide in surfactant production and application, which has theoretical and practical significance for safeguarding human health and safety.

Key words: fatty acid alkanolamides, surfactant, nitrosamine, ethanolamine compound, nitrosation mechanism