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711.
We report the diffusion coefficient and viscosity of popular rigid water models: two non-polarizable ones (SPC/E with three sites, and TIP4P/2005 with four sites) and a polarizable one (Dang-Chang, four sites). We exploit the dependence of the diffusion coefficient on the system size (Yeh and Hummer 2004 J. Phys. Chem. B 108 15873) to obtain the size-independent value. This also provides an estimate of the viscosity of all water models, which we compare to the Green-Kubo result. In all cases, a good agreement is found. The TIP4P/2005 model is in better agreement with the experimental data for both diffusion and viscosity. The SPC/E and Dang-Chang models overestimate the diffusion coefficient and underestimate the viscosity. 相似文献
712.
Amandine Calmet Abdelilah Amar Sophie Griveau Virginie Lair Eliane Sutter Francisco Javier Recio Philippe Brunswick Fethi Bedioui Michel Cassir 《Electroanalysis》2016,28(2):380-384
A non‐invasive device based on measurements of electrochemical skin conductance can detect small fiber neuropathy, a sweat gland dysfunction implicated in several diseases. The measurement is related to sweat composition and notably to chloride concentration. To optimize the electrode material, in vitro experiments are performed in mimetic sweat solutions. This work reports on the resistance to pitting corrosion of biocompatible stainless steels (AISI 304L, AISI 430, AISI 430T, D2205) in sweat mimicking electrolyte at pH 7 with variable chloride concentration, to determine the most sensitive material to sweat composition. AISI 430 is promising due to its high sensitivity to chloride concentration variations. 相似文献
713.
Mabrouk Majdi Marchand Mickael Russello Aldo Baronnet Jean Marie Lemont Florent 《Plasma Chemistry and Plasma Processing》2015,35(1):45-60
Plasma Chemistry and Plasma Processing - A process for the destruction of organic liquid waste has been developed in which a nontransferred arc plasma torch is operated with oxygen as the plasma... 相似文献
714.
Reactions of the in situ generated thiazoles 2 with aryl and alkyl isothiocyanates appear to be totally regioselective and give the unexpected 5‐(phenylthio)imidazolium‐4‐thiolates 3 . Such rapid interconversion of mesoionic compounds is explained by a 1,3‐dipolar addition to the C=N bond of the heterocumulene followed by tBuNCS elimination. Similar interactions with benzoyl isothiocyanate exclusively proceed on the C=S unsaturation of the heteroallene moiety and produce the 4‐(phenylthio)thiazolium‐5‐amidines 12 . Structural assignment of isolated imidazoles and thiazoles is based on 13C NMR data and chemically confirmed by the NaBH4 reduction of the alkylated derivatives 5 and 13 . Efforts to isomerize the starting mesoionic thiazole 2a without the use of tBuNCS are unsuccessful. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 10:16–26, 2000 相似文献
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Summary: A conjugated polymer ( P1 ) containing a pendant aldehyde was anodically prepared on ITO electrodes. Aminothiophenes could be captured by reacting with an aldehyde group located along the polymer backbone resulting in a robust azomethine bond. This was confirmed both spectroscopically and electrochromically. P1 undergoes absorbance and fluorescence bathochromic shifts when an aminothiophene is covalently linked to the aldehyde resulting from azomethine formation. Both the absorbance and fluorescence shifts are dependent on the aminothiophene used to form the azomethine bond. 相似文献
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