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环境友好材料:基于氨基酸离子液体的理化性质与毒性研究 被引量:2

Environmentally friendly materials:Physico-chemical properties and toxicity of amino acid derived ionic liquids
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摘要 制备了6种以氨基酸为阳离子的离子液体,并研究了熔点、玻璃转化温度、热稳定性、溶解性等重要的理化性质及毒性,为日后的应用奠定基础。结果表明,基Cl^(-)的离子液体熔点在90~100℃之间;而基于SO_(4)^(2-)的离子液体室温下为液态,无明显的熔点:符合"离子液体"的定义。仅一种离子液体有玻璃转化温度。6种离子液体在127~200℃之间发生了放热反应。所有的离子液体都能与水完全混溶,微溶或不溶于乙酸乙酯、正辛醇和乙醇。在毒性实验中,肌酸离子液体对螺旋藻的增殖无明显影响;L-组氨酸离子液体有一定的抑制作用,半数抑制浓度EC_(50)大于200 mg/L;甲硫氨酸离子液体有促进作用。所有的离子液体的GHS水生环境风险分类为第3级急性毒性或第4级慢性毒性,对环境的影响风险较小,可作为很好的环境友好材料。 6 Ionic liquids(ILs) were synthesized from 3 amino acids for cations and 2 inorganic acids for anions.Their physico-chemical properties,such as melting point,glass transition temperature and solvation property,as well as toxicity towards Spirulina platensis were studied.The melting points of Cl^(-) based ILs are between 90~100 ℃.The SO_(4)^(2-) based ILs are liquid at room temperature,without obvious melting points.Exothermal reactions took place between 127~200 ℃ All the ILs are fully miscible with water,slight soluble or insoluble in ethyl acetate,n-octanol and ethanol.Creatine based ILs have no obvious influence on the proliferation of Spirulina platensis.L-histidine based ILs inhibited the proliferation,with EC_(50) higher than 200 mg/L,whilst methionine based ILs stimulated that.The GHS Hazard to Aquatic Environment of all the ILs is categorized as classes Acute 3 or Chronic 4,corresponding to slight environmental hazard.Can be used as a good environmentally friendly material.
作者 庞俊峰 高国龙 王庆 陆坤 王殿二 PANG Jun-feng;GAOGuo-long;WANG Qing;LU Kun;WANG Dian-er(Everbright Environmental Technology(Jiangsu)Co.,Ltd.,Nanjing 211100,China;College of Environment and Civil Engineering,Jiangnan University,Wuxi 214122,China)
出处 《应用化工》 CAS CSCD 北大核心 2019年第S01期238-241,共4页 Applied Chemical Industry
关键词 氨基酸 离子液体 理化性质 毒性 amino acid ionic liquid physico-chemical property toxicity
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  • 1J G Huddleston,AE Visser,W M Reichert.Green Chem.,2001,3:156~164.
  • 2J G Huddleston,R D Rogers.Chem.Commun.,1998,16:1765 ~ 1766.
  • 3Y Ito,T Nohira.Electrochim.Acta,2000,45:2611 ~ 2622.
  • 4C M Gordon.Appl.Catal.A:General,2001,222:101 ~ 117.
  • 5D B Zhao,M Wu,Y Kou.Catal.Today,2002,74:157 ~ 189.
  • 6H W Zhang,K L Hong,J M Mays.Macromol.,2002,35:5738 ~ 5741.
  • 7A J Carmichael,D M Haddleton,S A F Bon.Chem.Commn.,2000,14:1237 ~ 1238.
  • 8S Z EI Abedin,N Borissenko,F Endres et al.Electrochem.Commun.,2004,6:422~426.
  • 9K Sekiguchi,M Atobe,T Fuchigami.Electrochem.Commun.,2002,4:881 ~ 885.
  • 10S V Dzyuba,R A Bartsch.Tetrahed.Lett.,2002,43:4657 ~ 4659.

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