High resolution extreme ultraviolet spectrometer for an electron beam ion trap

An extreme ultraviolet spectrometer has been developed for spectroscopic studies of highly charged ions with an electron beam ion trap. It has a slit-less configuration with a spherical varied-line-spacing grating that provides a flat focal plane for grazing incidence light. Alternative use of two different gratings enables us to cover the wavelength range 1-25 nm. Test observations with the Tokyo electron beam ion trap demonstrate the high performance of the present spectrometer such as a resolving power of above 1000.     

2D Superlattices for Efficient Energy Storage and Conversion

2D genuine unilamellar nanosheets, that are, the elementary building blocks of their layered parent crystals, have gained increasing attention, owing to their unique physical and chemical properties, and 2D features. In parallel with the great efforts to isolate these atomic-thin crystals, a unique strategy to integrate them into 2D vertically stacked heterostuctures has enabled many functional applications. In particular, such 2D heterostructures have recently exhibited numerous exciting electrochemical performances for energy storage and conversion, especially the molecular-scale heteroassembled superlattices using diverse 2D unilamellar nanosheets as building blocks. Herein, the research progress in scalable synthesis of 2D superlattices with an emphasis on a facile solution-phase flocculation method is summarized. A particular focus is brought to the advantages of these 2D superlattices in applications of supercapacitors, rechargeable batteries, and water-splitting catalysis. The challenges and perspectives on this promising field are also outlined.     

Detection of fluorescence from a mixed specimen consisting of micro particles attached to different fluorescent substances using a light waveguide incorporated optical TAS

A “ubiquitous human health care system” will require a monolithic optical total analysis system (TAS) consisting of waveguides and microfluidic channels based on a transparent resin chip. Together with the rapid development of the fluorescent marking method, fluorescence analysis by TAS of mixed-microparticle specimen attached to different fluorescent substances will be necessary. Towards realization of this, we here propose a novel method for using a part of the fluorescence acquired by irradiating microparticles with AC-modulated laser power as light dedicated to the discrimination of fluorescent substances. Since the light power for discrimination was extremely weak, we extracted effective signal components using a lock-in detection method. Then, by comparison with the signal of the original fluorescence, we could determine whether the fluorescence signal was from the microparticles attached to the fluorescent substance to be discriminated. Using a mixed specimen composed of microparticle-attached fluorescent substances with emission peaks of 520 nm and 600 nm, we found that 10% of the acquired fluorescence could successfully determine the specified fluorescent substance as a discrimination signal. The peak value of the discrimination signal was approximately double the amplitude of the stationary noise in the discrimination signal.

     

Ozonation of C.I. Reactive Yellow 3 and Further Decrease in Dissolved Organic Carbon Concentration by Post-Biodegradation

Using C.I. Reactive Yellow 3 as the target compound, the effect of the combined use of ozonation and post-biodegradation on the decrease in dissolved organic carbon (DOC) concentration was investigated, and the synergistic effect (the difference in the amounts of DOC removed by the biological process between solutions with and without ozonation) was estimated. A decrease in DOC concentration was observed during ozonation and ΔO₃/ΔDOC was decreased from 16.0 to 5.2 with increasing ozonation time. Moreover, an enhancement of biodegradability was shown. A further decrease in DOC concentration was observed during the biodegradation after ozonation. The total amount of DOC removed by the combined method was increased from 73.6 mg at 30 min to 159.9 mg at 4 h. The synergistic effect was in the range of 22.7 to 39.2 mg. BOD₅ was a better indicator of the synergistic effect than BOD₅/DOC.     

Pore structure of carbons coated on ceramic particles

Pore structure of carbon coated on ceramic particles by carbonization of precursor in a powder mixture at 900 °C was studied by focusing on the effects of substrate ceramics (MgO, TiO₂ and various phases of Al₂O₃) and of carbon precursor (poly(vinyl alcohol) (PVA), poly(ethylene terephthalate) (PET) and hydroxyl propyl cellulose (HPC)). By dissolving substrate MgO particles, carbon coated was found to have a high BET surface area, more than 1000 m²/g, which was almost the same as the value estimated from apparent surface area measured on carbon-coated MgO particles under the assumption of zero surface area of the substrate. The carbon separated was found to be rich in micropores from the analyses by DFT method and α_s plot. The dependence of the BET surface area on the amount of carbon coated on TiO₂ with a high surface area was the same for three carbon precursors, although the carbon yields from the precursors were slightly different. Porous Al₂O₃ substrates, γ-Al₂O₃as-received and that formed from Al(OH)₃ during carbonization, gave a high BET surface area, but dense Al₂O₃, α-Al₂O₃, gave a low surface area.     

XAFS Analysis for Niobium Carbide Particle Growth on Silica Support During Preparation Process

SiO₂-supported NbC catalysts were prepared by using temperature-programmed reactions (TPR). XAFS analysis confirmed that Nb₂O₅ was reduced to NbO₂ in the first TPR stage and converted into NbC in the second TPR stage. Nb particles grew only in the second TPR stage. Formation of highly dispersed NbC particles on SiO₂ surfaces was achieved.     

Polyacrylonitrile ultrafiltration membranes containing negatively charged groups for permeation and separation of dextran and dextransulfate

Ultrafiltration membranes of poly(acrylonitrile-co-sodium styrenesulfonate) [P(AN-co-SSS)] were prepared by casting the copolymer solution into water. The ultrafiltration rate of P(AN-co-SSS) membranes was controlled by adding poly(ethylene glycol) (PEG) of various molecular weights to the casting solution. The effect of the PEG addition on the membrane properties was examined. By using the P(AN-co-SSS) membranes, which possess various molecular weight cutoff (MWCO) properties, the permeation behaviors of dextran (D) and dextransulfate (DS) were compared. The P(AN-co-SSS) membranes markedly restricted the permeation of DS, owing to electrostatic barrier of the negatively charged groups in the membrane. The electrostatic sieve separation of DS and D, each having similar molecular size, with the membranes was also investigated. The membrane having negatively charged groups effectively rejected to DS with a high permselectivity. © 1994 John Wiley & Sons, Inc.     

粘弹性流体旋转流实验研究

利用粒子图像测速仪(PIV)对圆筒形容器内有自由表面变形的粘弹性流体旋转流动进行了实验研究.旋转流动由等速旋转的容器底面来驱动.实验工质为CTAC(十六烷基三甲基氯化铵界面活性剂)水溶液.测量了水、40×10-6、60×10-6和200×10-6CTAC水溶液在弗鲁德数为2.59至16.3范围内的旋转流动.PIV用来测量子午面内的二次流场,并从PIV图像中抽取自由面高度.结果表明在相似的弗鲁德数下,相比于水流CTAC水溶液旋转流动自由表面中心处的凹陷深度降低,随着溶液浓度或粘弹性升高,子午面内右上角的惯性涡被压缩且强度变得越来越弱.通过与水流动比较并做力平衡分析,定量估算了CTAC水溶液的第一正应力差或弱粘弹性.     

Modification and laboratory evaluation of a TSI ultrafine condensation particle counter (Model 3776) for airborne measurements

A butanol-type ultrafine condensation particle counter (UCPC, Model 3776, TSI, Inc., Shoreview, MN, USA), which can achieve a 50% detection efficiency diameter (d₅₀) of 2.5 nm using a capillary-sheath structure, was modified and tested in the laboratory for airborne measurements. The aerosol flow rate through the capillary is a key factor affecting the quantification of aerosol particle number concentrations. A pressure-dependent correction factor for the aerosol flow rate was determined using a newly added mass flow meter for the sheath flow and the external calibration system. The effect of particle coincidence in the optical sensing volume was evaluated using an aerosol electrometer (AE, Model 3068B, TSI, Inc.) as a reference. An additional correction factor for the coincidence effect was derived to improve the quantification accuracy at higher concentrations. The particle detection efficiency relative to the AE was measured for mobility diameters of 3.1–50 nm and inlet absolute pressures of 101–40 kPa. The pressure dependence of the d₅₀ value, asymptotic detection efficiency, and shape of the particle detection efficiency curve is discussed, along with simple theoretical calculations for the diffusion loss of particles and the butanol saturation ratio in the condenser.

© 2017 American Association for Aerosol Science     

Multiple evaluations of the removal of pollutants in road runoff by soil infiltration

Groundwater replenishment by infiltration of road runoff is expected to be a promising option for ensuring a sustainable urban water cycle. In this study, we performed a soil infiltration column test using artificial road runoff equivalent to approximately 11-12 years of rainfall to evaluate the removal of pollutants by using various chemical analyses and bioassay tests. These results indicated that soil infiltration treatment works effectively to remove most of the pollutants such as organic matter (chemical oxygen demand (CODMn) and dissolved organic carbon (DOC)), P species, polycyclic aromatic hydrocarbons (PAHs), numerous heavy metals and oestrogenic activities. Bioassay tests, including algal growth inhibition test, Microtox and mutagen formation potential (MFP) test, also revealed effective removal of toxicities by the soils. However, limited amounts of NO3, Mn, Ni, alkaline earth metals, perfluorooctane sulphonate (PFOS) and perfluorooctane sulphonamide (FOSA) were removed by the soils and they possibly reach the groundwater and cause contamination.