Attempt to estimate initial composition of the nucleus of homogenized garnet in pelitic gneisses from the Lützow-Holm Complex

The Tenth Symposium on Polar Science/Ordinary sessions: [OG] Polar Geosciences, Wed. 4 Dec. / Entrance Hall (1st floor), National Institute of Polar Researc

Growth history of garnet inferred from microstructures in pelitic gneisses from Akarui Point of the Lützow-Holm Complex

The Tenth Symposium on Polar Science/Ordinary sessions: [OG] Polar Geosciences, Wed. 4 Dec. / Entrance Hall (1st floor), National Institute of Polar Researc

Applicability of an Ionic Liquid Electrolyte to a Phosphorus‐Doped Silicon Negative Electrode for Lithium‐Ion Batteries

We investigated the applicability of an ionic liquid electrolyte to a phosphorus‐doped Si (P‐doped Si) electrode to improve the performance and safety of the lithium‐ion battery. The electrode exhibited excellent cycling performance with a discharge capacity of 1000 mA h g-1 over 1400 cycles in the ionic liquid electrolyte, whereas the capacity decayed at the 170th cycle in the organic electrolyte. The lithiation/delithiation reaction of P‐doped Si occurred a localized region in the organic electrolyte, which generated a high stress and large strain. The strain accumulated under repeated charge‐discharge cycling, leading to severe electrode disintegration. In contrast, the reaction of P‐doped Si proceeded uniformly in the ionic liquid electrolyte, which suppressed the electrode disintegration. The P‐doped Si electrode also showed good rate performance in the ionic liquid electrolyte; a discharge capacity of 1000 mA h g-1 was retained at 10 C

Electrochemical Lithiation and Delithiation Properties of FeSi2/Si Composite Electrodes in Ionic-Liquid Electrolytes

We investigated the applicability of ionic-liquid electrolytes to FeSi2/Si composite electrode for lithium-ion batteries. In conventional organic-liquid electrolytes, a discharge capacity of the electrode rapidly faded. In contrast, the electrode exhibited a superior cycle life with a reversible capacity of 1000 mA h g(Si)−1 over 850 cycles in a certain ionic-liquid electrolyte. The difference in the cycle life was explained by surface film properties. In addition, the rate performance of the FeSi2/Si electrode improved in another ionic-liquid electrolyte. Remarkably, lithiation of only Si in FeSi2/Si composite electrode occurred whereas each FeSi2- and Si-alone electrode alloyed with Li in the ionic-liquid electrolyte. FeSi2 certainly covered the shortcomings of Si and the FeSi2/Si composite electrode exhibited improved cycle life and rate capability compared to Si-alone electrode

Enhanced Permeability of Tetragastrin across the Rat Intestinal Membrane and Its Reduced Degradation by Acylation with Various Fatty Acids

ABSTRAC

Effect of Film-Forming Additive in Ionic Liquid Electrolyte on Electrochemical Performance of Si Negative-Electrode for LIBs

1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide (EMI-TFSA) is one of the promising ionic liquids as electrolyte solvent to enhance the electrochemical performance of Si electrode for Li-ion batteries (LIBs) because of its low viscosity and high conductivity. However, it has low stability against reduction and its reductive decomposition product inhibits Li+ insertion to electrodes, leading to poor cycling stability. To exert a potential of EMI-TFSA, we employed vinylene carbonate (VC) as film-forming additive. Si electrode exhibited very high cycling stability and rate capability in 20 vol.% VC-added EMI-TFSA-based electrolyte. In addition, by replacing TFSA anion with bis(fluorosulfonyl)amide (FSA) for Li salt and ionic liquid solvent, an excellent cycling performance and outstanding rate capability was achieved. VC cannot only fabricate a good surface film but also lower the interaction between Li+ and FSA-, providing smooth desolvation of FSA- to obtain better high-rate performance. Non-flammability of the VC-added electrolytes was confirmed by fire resistance test in closed-system: no ignition was observed even at 300°C. Consequently, we found that mixture electrolyte consisted of EMI-based ionic liquid and VC, especially 1 M LiFSA/EMI-FSA with 20 vol.% VC, is a prospective candidate for simultaneously enhancing the electrochemical performance of Si electrode as well as safety of LIBs

Nanoparticles decorated with proteolytic enzymes, a promising strategy to overcome the mucus barrier

The intestinal mucus gel layer represents a stumbling block for drug adsorption. This study is aimed to formulate a nanoparticulate system able to overcome this barrier by cleaving locally the glycoprotein substructures of the mucus. Mucolytic enzymes such as papain (PAP) and bromelain (BRO) were covalently conjugated to poly(acrylic acid) (PAA). Nanoparticles (NPs) were then formulated via ionic gelation method and characterized by particle size, zeta potential, enzyme content and enzymatic activity. The NPs permeation quantified by rotating tube studies was correlated with changes in the mucus gel layer structure determined by pulsed-gradient-spin-echo NMR (PGSE-NMR), small-angle neutron scattering (SANS) and spin-echo SANS (SESANS). PAP and BRO functionalized NPs had an average size in the range of 250 and 285 nm and a zeta potential that ranged between -6 and -5 mV. The enzyme content was 242 μg enzyme/mg for PAP modified NPs and 253 μg enzyme/mg for BRO modified NPs. The maintained enzymatic activity was 43% for PAP decorated NPs and 76% for BRO decorated NPs. The rotating tube technique revealed a better performance of BRO decorated NPs compared to PAA decorated NPs, with a 4.8 fold higher concentration of NPs in the inner slice of mucus. Addition of 0.5wt% of enzyme functionalized NPs to 5wt% intestinal mucin led to c.a. 2 fold increase in the mobility of the mucin as measured by PGSE-NMR indicative of a significant break-up of the structure of the mucin. SANS and SESANS measurements further revealed a change in structure of the intestinal mucus induced by the incorporation of the functionalized NPs mostly occurring at a lengthscale longer than 0.5 μm. Accordingly, BRO decorated NPs show higher potential then PAP functionalized NPs as mucus permeating drug delivery systems