TY - JOUR
T1 - Enhancement of π–π aromatic interactions between hydrophobic Ionic Liquids and Methylene Blue for an optimum removal efficiency and assessment of toxicity by microbiological method
AU - Kermanioryani, Massoud
AU - Mutalib, M. Ibrahim A.
AU - Kurnia, Kiki Adi
AU - Lethesh, Kallidanthiyil Chellapan
AU - Krishnan, Sooridarsan
AU - Leveque, Jean Marc
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/11/20
Y1 - 2016/11/20
N2 - Due to their harmful effects on human's life and aquatic environments, designing easy and swift yet efficient methodologies to remove pollutants from water stream is one of the important tasks of the scientific community. Among the pollutants, dyes have a significant role on water pollution, because their presence, even in low concentration, impacts the aquatic life by preventing the photosynthesis process and it can be considered as toxic chemicals endangering the human's health. In this study three newly synthesized Task Specific Ionic Liquids (TSILs) incorporating different types of aromatic group on imidazolium ring namely, 1-Butyl-3-Benzoimidazolium bis(trifluoromethylsulfonyl)imide [BzBIm][NTf2]; 1-Butyl-2-Phenyl-imidazolium bis(trifluoromethylsulfonyl)imide [BPhIm][NTf2]; and 1-Benzyl-3-butyl-imidazolum bis(trifluoromethylsulfonyl)imide [BnBIm][NTf2] have been employed to remove swiftly heavy loads (up to 1,500 ppm) of cationic Methylene Blue dye (MB) from aqueous solution without pH adjustment. The results showed that the presence of additional aromatic groups has a significant effect on the extraction efficiency of MB removal through enhancement of the π–π interactions between ILs and the aromatic structure of MB. Conductor-like Screening Model for Real Solvent (COSMO-RS) was used to analyse the IL-MB interaction in the studied systems. Finally, an original microbiological method has been designed not only to assess the toxicity of aqueous solution before and after the extraction process to reveal the industrial potential of this methodology but also to highlight the high hydrophobicity of these new TSILs.
AB - Due to their harmful effects on human's life and aquatic environments, designing easy and swift yet efficient methodologies to remove pollutants from water stream is one of the important tasks of the scientific community. Among the pollutants, dyes have a significant role on water pollution, because their presence, even in low concentration, impacts the aquatic life by preventing the photosynthesis process and it can be considered as toxic chemicals endangering the human's health. In this study three newly synthesized Task Specific Ionic Liquids (TSILs) incorporating different types of aromatic group on imidazolium ring namely, 1-Butyl-3-Benzoimidazolium bis(trifluoromethylsulfonyl)imide [BzBIm][NTf2]; 1-Butyl-2-Phenyl-imidazolium bis(trifluoromethylsulfonyl)imide [BPhIm][NTf2]; and 1-Benzyl-3-butyl-imidazolum bis(trifluoromethylsulfonyl)imide [BnBIm][NTf2] have been employed to remove swiftly heavy loads (up to 1,500 ppm) of cationic Methylene Blue dye (MB) from aqueous solution without pH adjustment. The results showed that the presence of additional aromatic groups has a significant effect on the extraction efficiency of MB removal through enhancement of the π–π interactions between ILs and the aromatic structure of MB. Conductor-like Screening Model for Real Solvent (COSMO-RS) was used to analyse the IL-MB interaction in the studied systems. Finally, an original microbiological method has been designed not only to assess the toxicity of aqueous solution before and after the extraction process to reveal the industrial potential of this methodology but also to highlight the high hydrophobicity of these new TSILs.
KW - Aromatic group
KW - COSMO-RS
KW - Methylene Blue removal
KW - Microbiological method
KW - Task Specific Ionic Liquids
UR - http://www.scopus.com/inward/record.url?scp=84990944578&partnerID=8YFLogxK
U2 - 10.1016/j.jclepro.2016.07.193
DO - 10.1016/j.jclepro.2016.07.193
M3 - Article
AN - SCOPUS:84990944578
SN - 0959-6526
VL - 137
SP - 1149
EP - 1157
JO - Journal of Cleaner Production
JF - Journal of Cleaner Production
ER -