Converter configurations and switching frequency for a GTO reactivepower compensator

This paper compares two converter configurations for a multi-10 MVA gate-turn-off (GTO) reactive power compensator (STATCOM) from the viewpoints of converter connection and switching frequency. One is a single-bridge system consisting of a three-phase bridge converter unit and a transformer. Its pulsewidth modulation (PWM) frequency varies from 450 to 1800 Hz, and its line frequency is 50 Hz. The other is a multiconnected converter system consisting of plural, single-, or three-phase converter units and transformers. Its switching frequencies are chosen to be the lowest possible. The evaluated items are harmonic distortion, power loss, GTO utilization factor, and control response. Our simulation study shows that the multiconnected converter system with the lowest switching frequency is superior to the single-bridge system with the higher switching frequency in every case, even when there are severe line faults requiring very quick response. A new control strategy is adopted for obtaining quick response     

Structural approach to nanoscience: a case study of complex and cluster formation in ZnBr2–ZnCl2 melts

Although the melt structure of glass-forming ZnCl₂ has so far been well studied, there exists quite little information on the structural change due to anion-substitution. In the present work, the short-range structure of ZnCl₂–ZnBr₂ mixture melts was analyzed systematically by time-of-flight pulsed neutron diffraction techniques, Raman spectroscopy, molecular orbital calculations, and molecular dynamics simulations. According to radial distribution analysis, it was found that there were tetrahedral structural units of ligand-substituted [ZnCl_nBr_4−n]²⁻ (n=0–4) in these melts, not implying the simple mixing of [ZnCl₄]²⁻ and [ZnBr₄]²⁻ units. Further detailed estimation indicated that the ligand-substituted complex anions were linked with each other by sharing a common anion.     

The effect of atmospheric plasma treatment of recycled carbon fiber at different plasma powers on recycled carbon fiber and its polypropylene composites

To increase the mechanical properties of recycled carbon fiber-reinforced polypropylene (PP) composites, recycled carbon fibers (RCF) were subjected to atmospheric plasma treatment at different plasma powers (100, 200, and 300 W). The changes on surface topography and roughness of RCF were examined by atomic force microscopy. Plasma treatment of RCF increased the roughness value of RCF. The variation of surface elemental compositions and tensile strength of RCF were determined by using X-ray photoelectron spectroscopy and tensile test, respectively. Plasma-treated RCF-reinforced PP composites were fabricated using high speed thermo-kinetic mixer. Plasma treatment of RCF at 100 W increased the tensile and flexural strength values of RCF-reinforced PP composites considerably by 17 and 11%, respectively. However, plasma treatment of RCF at higher plasma powers (200 W and 300 W) decreased tensile and flexural strength values of composites because of the etching of RCF. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47131.     

Chiral lewis acid-catalyzed enantioselective michael reactions in water

Asymmetric Michael reactions of ß-ketoesters with enones were effectively catalyzed by complexes of silver salts and BINAP derivatives in water. The reactions have proved to give Michael adducts in high yields with high enantioselectivities. These reactions are the first example of Lewis acid-catalyzed asymmetric Michael reactions in water.     

Separation of C6H6 and C6H12 from H2 using ionic liquid/PVDF composite membrane

Ionic liquid/polyvinylidene fluoride composite membrane was successfully prepared by impregnation method and used for the separation on organic chemical hydride process. The separation factors of C₆H₆/H₂ and C₆H₁₂/H₂ in the ternary mixture system were 7500 and 300, respectively. The ionic liquid membrane showed an excellent possibility as a technology of H₂ purification in the organic chemical hydride process by removing aromatic hydrocarbon and cycloalkane simultaneously from the ternary system. © 2015 American Institute of Chemical Engineers AIChE J, 62: 624–628, 2016     

Novel functional polymers: Poly(dimethylsiloxane)–polyamide multiblock copolymer. III. Synthesis and surface properties of disiloxane–aromatic polyamide multiblock copolymer

Disiloxane–aromatic polyamide(aramid) multiblock copolymers(2SiPASs) were synthesized using 1,3-bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane(BATS) as an analog of aramidsilicone resin consisting of aromatic polyamide and poly(dimethylsiloxane) (PDMS). 2SiPASs afford a transparent and toughened plastic film. The surface properties of 2SiPAS were investigated by X-ray photoelectron spectroscopy (xps) and static contact angle measurement. The results of surface analysis suggested that BATS content of the 2SiPAS surface increased with increasing BATS content in bulk. The interaction between the platelets and the 2SiPAS surface was found to be very weak when the BATS content reached 26 wt % in bulk. © 1996 John Wiley & Sons, Inc.     

Development of Fluorogenic Probes for Rapid High-Contrast Imaging of Transient Nuclear Localization of Sirtuin 3

Protein labeling using fluorogenic probes enables the facile visualization of proteins of interest. Herein, we report new fluorogenic probes consisting of a rationally designed coumarin ligand for the live-cell fluorogenic labeling of the photoactive yellow protein (PYP)-tag. On the basis of the photochemical mechanisms of coumarin and the probe–tag interactions, we introduced a hydroxy group into an environment-sensitive coumarin ligand to modulate its spectroscopic properties and increase the labeling reaction rate. The resulting probe had a higher labeling reaction rate constant and a greater fluorescence OFF–ON ratio than any previously developed PYP-tag labeling probe. The probe enabled the fluorogenic labeling of intracellular proteins within minutes. Furthermore, we used our probe to investigate the localization of sirtuin 3 (SIRT3), a mitochondrial deacetylase. Although the nuclear localization of SIRT3 has been controversial, this transient nuclear localization was clearly captured by the rapid, high-contrast imaging enabled by our probe.     

Solvent- and Light-Sensitive AIEE-Active Azo Dye: From Spherical to 1D and 2D Assemblies

Fluorescent molecular assembly systems provide an exciting platform for creating stimuli-responsive nano- and microstructured materials with optical, electronic, and sensing functions. To understand the relationship between (i) the plausible molecular structures preferentially adopted depending on the solvent polarity (such as N,N-dimethylformamide [DMF], tetrahydrofuran [THF], and toluene), (ii) the resulting spectroscopic features, and (iii) self-assembled nano-, micro-, and macrostructures, we chose a sterically crowded triangular azo dye (3Bu) composed of a polar molecular core and three peripheral biphenyl wings. The chromophore changed the solution color from yellow to pink-red depending on the solvent polarity. In a yellow DMF solution, a considerable amount of the twisted azo form could be kept stable with the help of favorable intermolecular interactions with the solvent molecules. By varying the concentration of the DMF solution, the morphology of self-assembled structures was transformed from nanoparticles to micrometer-sized one-dimensional (1D) structures such as sticks and fibers. In a pink-red toluene solution, the periphery of the central ring became more planar. The resulting significant amount of the keto-hydrazone tautomer grew into micro- and millimeter-sized 1D structures. Interestingly, when THF-H₂O (1:1) mixtures were stored at a low temperature, elongated fibers were stacked sideways and eventually developed into anisotropic two-dimensional (2D) sheets. Notably, subsequent exposure of visible-light-irradiated sphere samples to solvent vapor resulted in reversible fluorescence off↔on switching accompanied by morphological restoration. These findings suggest that rational selection of organic dyes, solvents, and light is important for developing reusable fluorescent materials.     

加速器质谱测量129I方法的改进

在筑波大学的12UD串列加速器上开发了一套改进的129I加速器质谱(AMS)测量方法,包括在120°磁铁后安装了一副自行设计制作有静电偏转板,有效改善了对127I束流和129I计数的测量;采用97MoO2分子导航束稳定加速器端电压,加速器的端电压能稳定在几天内不超过0.1%,结合二次剥离,取得了满意的测量效果.用该方法测得AgI试剂样品的本底水平为7.83×10-13.对129I/127I比值范围为(4.92～0.28)×10-10的一系列样品的测量不确定度在7%以下,准确度较前有所提高.