30 research outputs found

    Ultrafast structure and dynamics in ionic liquids: 2D-IR spectroscopy probes the molecular origin of viscosity

    Get PDF
    The viscosity of imidazolium ionic liquids increases dramatically when the strongest hydrogen bonding location is methylated. In this work, ultrafast two-dimensional vibrational spectroscopy of dilute thiocyanate ion ([SCN] -) in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C4C1im][NTf2]) and 1-butyl-2,3- dimethylimidazolium bis(trifluoromethylsulfonyl)imide ([C4C 1C12im][NTf2]) shows that the structural reorganization occurs on a 26 ± 3 ps time scale and on a 47 ± 15 ps time scale, respectively. The results suggest that the breakup of local ion-cages is the fundamental event that activates molecular diffusion and determines the viscosity of the fluids. © 2014 American Chemical Society

    Flora of the Nichols Arboretum, Ann Arbor, MIa thesis submitted in partial fulfillment ... for th

    Full text link
    Master of ScienceNatural Resources and EnvironmentUniversity of Michiganhttp://deepblue.lib.umich.edu/bitstream/2027.42/101638/1/39015052696229.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/101638/2/39015052696229.pd

    Efficient Polymerization Inhibition Systems for Acrylic Acid Distillation: New Liquid-Phase Inhibitors

    No full text
    Phenothiazine and other compounds with similar structures, namely, phenoxazine, promazine, promazine hydrochloride, <i>N</i>,<i>N</i>′-dimethylphenazine, carbazole, <i>N</i>-ethylcarbazole, <i>N</i>-benzylphenothiazine, and <i>N</i>-(1-phenylethyl)­phenothiazine were tested as liquid-phase inhibitors for acrylic acid. N-Alkylated phenothiazine (PTZ) derivatives, such as <i>N</i>-benzylphenothiazine and especially <i>N</i>-(1-phenylethyl)­phenothiazine, showed improved efficiency for liquid-phase inhibition, in comparison with PTZ. It was also shown that N-alkylated PTZ derivatives could be used in combination with nitroso compounds that can be employed as vapor-phase inhibitors. The combination of <i>N</i>-(1-phenylethyl)­phenothiazine and nitrosobenzene showed superior liquid-phase-inhibition efficiency, with time to gelation of >122 h, in comparison with 64 h obtained with PTZ alone. The structure of liquid-phase inhibitors had no influence on the extent of Michael addition reactions during heating of acrylic acid
    corecore