Synthesis and mesomorphic properties of mesogens containing 1,1,2,2-tetrahydroperfluorodecaoxy terminal chains

One series of two-ring and two series of three-ring mesogens with 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-heptadecafluorodecaoxy terminal chains containing tolane or biphenyl units have been synthesized. Their mesomorphic properties were observed and measured by optical polarizing microscopy and differential scanning calorimetry. The three-ring mesogens only exhibit a wide smectic C phase when the length of their hydrocarbon chains is intermediate.     

A family of single‐isomer,dicationic cyclodextrin chiral selectors for capillary electrophoresis: Mono‐6A‐ammonium‐6C‐butylimidazolium‐β‐cyclodextrin chlorides

The first member of the single‐isomer, dicationic cyclodextrin (CD) family, 6^A‐ammonium‐6^C‐butylimidazolium‐β‐cyclodextrin chlorides (AMBIMCD), has been synthesized, analytically characterized, and used to separate a variety of acidic enantiomers and amino acids by CE. Starting from mono‐6^A‐azido‐β‐cyclodextrin, the cationic imidazolium and ammonium moieties were subsequently introduced onto primary ring of β‐cyclodextrin via nucleophilic addition and Staudinger reaction. The analytically pure AC regio‐isomer CD was further obtained via column chromatography. This dicationic CD exhibited excellent enantioselectivities for selected analytes at concentration as low as 0.5 mM, which were even better than those of its mono‐imidazolium or ammonium‐substitued counterpart CDs at 10 equivalent concentrations. The effective mobilities of all studied analytes were found to decrease with the concentration of AMBIMCD. Inclusion complexation in combination with eletrostatic interactions seemed to account for the enhanced chiral discrimination process.     

Optimal Conditions for Existence of Vesicles Under Electric Field

Giant vesicles have been of intense interest as the model system for cell membranes. To bring numerous applications of the vesicles into full play, the existence time of the vesicles becomes particularly important. In this work, we explored the existence time of the vesicles in distilled water under four kinds of representative alternative current (AC) electric fields with different energizing time. When the application time of AC electric field reached 1 hour, the existence time of the vesicles reached the maximum value. As the applied electric field time increased, the existence time of the vesicles decreased. Thus, after obtaining the best vesicles on the carbon fiber electrode, disconnecting the external electric field is very necessary. Based on the in situ observation using inverted microscope, the disappearing phenomena of the vesicles were presented. In addition, it is found that vesicles in phosphate buffer solutions (PBSs) can last about 2–3 days when the electric field was applied for 1 hour, which was much longer than that in distilled water.     

SYNTHESIS OF CeO2 NANOPARTICLES IN W/ O MICROEMULSION

The phase composition and properties of microemulsion system of Titron N-101 / n-pentanol/ n-octane/ water (ammonia solution) were studied. CeO₂ nanopaticles were prepared by the reaction of cerous nitrate.     

Seasonal variation of 129I species in the Baltic Proper

Iodine speciation plays a significant role in iodine volatilizing into atmosphere from the seas, as well as serving as a biological indicator. Despite this importance, the data on iodine species revealed inconclusive evidence of what factors controlling speciation transformation. We here present new data on profiles of ¹²⁹I speciation in the Baltic Proper during November 2009. Along with the two earlier investigations (August 2006 and April 2007), an assessment of seasonal variation of ¹²⁹I species is presented. The results show that, due to the anoxic nature of Baltic Proper, presence of ¹²⁹IO₃ ^? in the Baltic Proper does not follow an obvious seasonal cycle, as the case with ¹²⁹I^?. Concentrations of ¹²⁹I^? in the Baltic Proper exhibit higher values in summer than the other two seasons (spring and winter), which might be associated with degrading of organic matter and release from sediment to water column that is more pronounced during summer. ¹²⁹I^? in surface water from the three seasons does not reflect the release function from the reprocessing facilities during the period April 2007 to November 2009. Consequently variability of ¹²⁹I^? in surface seawater of the Baltic Proper depends, to some extent, on local physical as well as biochemical conditions.     

The behavior of technetium in technetium-scrubbing stage of PUREX process

Technetium decontamination factor as a function of the acidity, flow ratio, scrubbing stage number was investigated by counter-current cascade experiments or mixer-settler batch tests. Results showed that the acidity of the scrubbing acid has little influence on the decontamination factor of technetium when the acidity was kept in the range of 4.5–6 M. The most effective method to increase the decontamination factor is to lower the feed-to-acid flow ratio. Keeping other condition same the factor increased to 10.3 from 3.1 when feed-to-acid ratio changed to 4 from 5.6. The loss of uranium and plutonium can be recovered through a re-extraction technology.     

Effect of additives on the structure and electrochemical performance of mesoporous nickel hydroxide

Nickel hydroxide mesoporous structures are synthesized by a simple method in the presence of different additives (oxalic acid, aminoacetic acid, and sulfosalicylic acid). Structural characterizations reveal that the additives can affect the crystal structure, increase the specific surface area, and reduce the pore size of the products. The electrochemical properties of the synthesized Ni(OH)₂ samples are dependent on their crystal phase, surface area, and pore size distribution. Mesoporous β-Ni(OH)₂ with poor crystallinity shows high specific capacitances at different current densities and excellent cycling ability. A highest specific capacitance of 1,693 F?g^?1 can be achieved at a scan rate of 5 mV?s^?1. The results suggest its potential application in electrochemical supercapacitors.     

Electrochemical performance of a nonaqueous rechargeable lithium-air battery

Nonaqueous rechargeable lithium-air battery has so high specific capacity and specific energy that it is being widely researched by academia, corporation, and different research institutes. When used in dried air and absorbing oxygen form the air, this battery is called lithium-air battery, and its specific capacity based on cathode active material (oxygen) is infinite. However, its cycle performance is very limited as reported by the state-of-the-art researches. This cycle problem is mainly caused by instability of electrolyte. Based on electroanalysis of materials’ electrochemical property, a stable electrolyte solvent (sulfolane) and a lithium salt LiBF₄ are selected as electrolytes in this work. Coupled with other eligible battery materials and careful assembly, the lithium-air battery exhibits favorable cycle performance. Above all, this lithium-air system is evaluated objectively in this paper.