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L-n-hexyl-3-methylimidazolium

The ionic liquid l-n-hexyl-3-methylimidazolium bis(trifiuorosulfonyl)imide, [hmim] [TfaN], was synthesized and characterized using standard procedures [17-19] at the University of Notre Dame. The ionic liquid l-(3-aminopropyl)-3-methylimidazolium bis(trifiuoromethylsulfonyl)imide, [H2NC3H5mim][Tf2N], was also synthesized and characterized at the University of Notre Dame [20]. [Pg.189]

Glycidyl methacrylate (purity 98 %) was purchased fiom Aldrich. Ionic liquids based on 1-n-ethyl-3-methyliinidazolium (EMIm), l-n-butyl-3-methylimidazolium (BMhn), 1-n-hexyl-3-methylimidaJ5Dlium (HMhn) with dififeent anions such as CT, BF4", PFg wo e prepared according to the procedures reported previously. Copolymerization of glycidyl methacrylate (GMA) and CO2 were carried out in a 50 mL stainless steel autoclave equipped with a... [Pg.865]

Chakrabarty, D., Chakraborty, A., Seth, D., and Sarkar, N. 2005. Effect of water, methanol, and acetonitrile on solvent relaxation and rotational relaxation of Coumarin 153 in neat l-hexyl-3-methylimidazolium hexafluorophosphate. J. Phys. Chem. A 109, 1764-1769. [Pg.245]

Gomez, E. Calvar, N. Dominguez, I. Dominguez A. (2006c). Physical properties of the ternary mixture ethanol water l-hexyl-3-methylimidazolium chloride at 298.15 K. Phys.Chem.Licj. 44,4 (2006) 409-417. [Pg.133]

When Br0nsted acidic ILs l-hexyl-3-methylimidazolium tetrafluoroborate [HMIM]BF4 (Lu et al., 2007) and N-methyl-pyrrolidonium tetrafluoroborate [HNMP]Bp4 (Zhao et al., 2007) were used for desulfurization in the presence of H2O2, sulfur compounds can be deeply removed due to formation of hydroxyl radicals. For [HMIM]BF4the DBT remotion was 93% when a mixture of 3.2 mL of model oil and 5.0 mL of the IL were stirring at 90 °C during 6 h. In the case of [HNMP]BF4 the efficiency of sulfur extraction was 99.4% for fuel diesel (total sulfur 3240 ppm) at ratio of 1 1 and 2 h of reaction time at 60 °C. The IL was recycled 7 times without a significant decrease in desulfurization. [Pg.578]

Letcher, T. M. Reddy, P. (2005). Ternary (liquid + liquid) equilibria for mixtures of 1-hexyl-3-methylimidazolium (tetrafluoroborate or hexafluoroborate)+ benzene+an alkane atT=298.2 K andp=0.1 MPa, /, Chem. Thermodyn. 37,415-421, ISSN 0021-9614. Letcher, T. M. Deenadayalu, N. Soko, B. Ramjugernath, D. Naicker, P. K. (2003). Ternary liquid-liquid equilibria for mixtures of l-methyl-3-octylimida-zolium chloride + an alkanol + an alkane at 298.2 K and 1 bar. /. Chem. Eng. Data, 48, 904-907, ISSN 1520-5134. [Pg.618]

E) l-Ethyl-3-methylimidazolium n-hexyl sulfate (IL) water (1 1)—(polar phase)/ sodium dodecyl sulfate (SDS)/toluene-pentanol (1 1) ... [Pg.226]


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1-Hexyl-3-methylimidazolium

Hexyl

L- -3-methylimidazolium

Methylimidazolium

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