Influence of oxygen functionalities on the environmental impact of imidazolium based ionic liquids

被引:63
作者
Deng, Yun [1 ]
Besse-Hoggan, Pascale [2 ,3 ]
Sancelme, Martine [2 ]
Delort, Anne-Marie [2 ,3 ]
Husson, Pascale [1 ]
Gomes, Margarida F. Costa [1 ]
机构
[1] Univ Blaise Pascal, Clermont Univ, Lab Thermodynam & Interact Mol, F-63171 Aubiere, France
[2] Univ Blaise Pascal, Clermont Univ, Lab Synth & Etude Syst Interet Biol, F-63171 Aubiere, France
[3] CNRS, UMR6504, F-63171 Aubiere, France
关键词
Ionic liquids; Toxicity; Biodegradability; Aqueous solubility and diffusivity; Octanol/water partition coefficient; WATER PARTITION-COEFFICIENTS; DIFFUSION-COEFFICIENTS; BIODEGRADATION; CONDUCTIVITIES; IDENTIFICATION; TOXICITY;
D O I
10.1016/j.jhazmat.2011.10.024
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Several physico-chemical properties relevant to determine the environmental impact of ionic liquids - aqueous solubility, octanol-water partition coefficient and diffusion coefficients in water at infinite dilution - together with toxicity and biodegradability of ionic liquids based on 1-alkyl-3-methylimidazolium cations with or without different oxygenated functional groups (hydroxyl, ester and ether) are studied in this work. The presence of oxygen groups on the imidazolium cation reduces the toxicity of ionic liquids 1-alkyl-3-methylimidazolium with bis(trifluoromethylsulfonyl)imide or octylsulfate anions and simultaneously decreases the value of their octanol-water partition coefficient. The presence of ester functions renders the ionic liquids more easily biodegradable, especially for long alkyl side-chains in the cation but leads to hydrolysis with the formation of reaction products that accumulate. The imidazolium ring is resistant to biodegradability and to abiotic degradation. The oxygen functionalised ionic liquids are more soluble in water and, diffuse more slowly in this medium. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:165 / 174
页数:10
相关论文
共 47 条
[21]   Anaerobic biodegradability of ionic liquid cations under denitrifying conditions [J].
Neumann, Jennifer ;
Grundmann, Olav ;
Thoeming, Jorg ;
Schulte, Michael ;
Stolte, Stefan .
GREEN CHEMISTRY, 2010, 12 (04) :620-627
[22]  
OECD, OECD GUID, P117
[23]  
OECD, OECD GUID, P107
[24]  
OECD, 1995, GUID TEST CHEM WAT S, P105
[25]  
OECD, 2006, SLOWS TIRR METH, P123
[26]   Molecular solutes in ionic liquids: A structural, perspective [J].
Padua, Agilio A. H. ;
Gomes, Margarida F. Costa ;
Lopes, Jose N. A. Canongia .
ACCOUNTS OF CHEMICAL RESEARCH, 2007, 40 (11) :1087-1096
[27]   Influence of Ester Functional Groups on the Liquid-Phase Structure and Solvation Properties of Imidazolium-Based Ionic Liquids [J].
Pensado, Alfonso S. ;
Padua, Agilio A. H. ;
Gomes, Margarida F. Costa .
JOURNAL OF PHYSICAL CHEMISTRY B, 2011, 115 (14) :3942-3948
[28]   Identification of Metabolites Involved in the Biodegradation of the Ionic Liquid 1-Butyl-3-methylpyridinium Bromide by Activated Sludge Microorganisms [J].
Pham, Thi Phuong Thuy ;
Cho, Chul-Woong ;
Jeon, Che-Ok ;
Chung, Yun-Jo ;
Lee, Min-Woo ;
Yun, Yeoung-Sang .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (02) :516-521
[29]   Applications of ionic liquids in the chemical industry [J].
Plechkova, Natalia V. ;
Seddon, Kenneth R. .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (01) :123-150
[30]   Carbon catabolite repression in Pseudomonas: optimizing metabolic versatility and interactions with the environment [J].
Rojo, Fernando .
FEMS MICROBIOLOGY REVIEWS, 2010, 34 (05) :658-684