Generation of 0.1 THz coherent synchrotron radiation with compact S-band linac at AIST

The 0.1 THz coherent synchrotron radiation (CSR) was successfully generated in the 90° bending magnet of the compact S-band linac with the achromatic arc section using the ultra-short electron bunch which has the energy of 40 MeV, the bunch charge of about 1nc and the bunch length less than 1 ps (rms). The electron bunch compression of 1 nC electron bunch was achieved less than 1 ps (rms) by controlling the Q-magnets in the achromatic arc section as the bunch length was measured by the rms bunch length monitor.     

分子束外延法在Sapphire衬底上生长的Zn1－xMgxO薄膜折射率及厚度的测试

利用偏振光椭圆率测量仪对分子束外延(MBE)法在Sapphire衬底上生长的Zn_1-xMg_xO 薄膜的薄膜折射率和厚度进行了测试. 结合ICP法测得的薄膜中的Mg组成量，经数值拟合，导出表征薄膜厚度与薄膜生长条件、薄膜折射率与薄膜中的Mg组成量之间关系的曲线，为MBE法在Sapphire衬底上生长Zn_1-xMg_xO 薄膜时控制薄膜厚度以及在制作Zn_1-xMg_xO 薄膜的波导时控制薄膜的折射率提供了理论依据. 关键词： ZnMgO薄膜 偏振光椭圆率测量仪 折射率 分子束外延(MBE)     

Photochemical ligand substitution reactions of fac-[Re(bpy)(CO)3Cl] and derivatives

Excitation by high-energy light, such as that of 313 nm wavelength, induces a photochemical ligand substitution (PLS) reaction of fac-[Re(bpy)(CO)3Cl] (1a) to give the solvento complexes (OC-6-34)- and (OC-6-44)-[Re(bpy)(CO)2(MeCN)Cl] (2 and 3) in good yields. The disappearance quantum yield of 1a was 0.01+/-0.001 at 313 nm. The products were isolated, and X-ray crystallographic analysis was successfully performed for 2. Time-resolved IR measurements clearly indicated that the CO ligand dissociates with subpicosecond rates after excitation, leading to vibrationally hot photoproducts, which relax within 50-100 ps. Detailed studies of the reaction mechanism show that the PLS reaction of 1a does not proceed via the lowest vibrational level in the 3MLCT excited state. The PLS reaction gives 2 and (OC-6-24)-[Re(bpy)(CO)2(MeCN)Cl] (5) as primary products, and one of the products, 5, isomerizes to 3. This type of PLS reaction is more general, occurring in various fac-rhenium(I) diimine tricarbonyl complexes such as fac-[Re(X2bpy)(CO)3Cl] (X2bpy=4,4'-X2-bpy; X=MeO, NH2, CF3), fac-[Re(bpy)(CO)3(pyridine)]+, and fac-[Re(bpy)(CO)3(MeCN)]+. The stable photoproducts (OC-6-44)- and (OC-6-43)-[Re(bpy)(CO)2(MeCN)(pyridine)]+ and (OC-6-32)- and (OC-6-33)-[Re(bpy)(CO)2(MeCN)2]+ were isolated. The PLS reaction of rhenium tricarbonyl-diimine complexes is therefore applicable as a general synthetic method for novel dicarbonyls.     

Preparation of cadmium‐containing brown rice grains as calibration standards for X‐ray fluorescence analysis of cadmium in rice grains

A preparation method for Cd‐containing brown rice grains as calibration standards was developed for X‐ray fluorescence (XRF) analysis of Cd in rice grains. Calibration standards were prepared by adding 10 g of base rice grains (from Japan) to 100 ml of methanol containing 5?100 µg of Cd. The mixture was heated, cooled, and stored in a silica gel desiccator. Seven grams of each calibration standard was packed into a polyethylene cup (32‐mm internal diameter and 23‐mm height) covered with a 6‐µm‐thick polypropylene film and then subjected to XRF analysis. The calibration curves of Cd in brown and white rice grains showed good linearity in 0.50?10 mg kg^?1. The detection limits of Cd in brown and white rice grains were 0.14 and 0.12 mg kg^?1, respectively. The slopes of the calibration curves for Cd in brown and white rice grains were slightly different owing to absorption effects. The absorption effects were corrected using the ratio of the intensity of Cd Kα to that of Rh Kα‐Compton scattering. After correction, the calibration curves of Cd in brown and white rice grains showed identical slopes. The spike test for 5 mg kg^?1 of Cd in white rice grains (from Thailand), using the corrected calibration curves, showed quantitative recoveries (92?97%). Copyright © 2013 John Wiley & Sons, Ltd.     

Comparative study of oxidative stability of sunflower and cotton biodiesel through P-DSC

Biodiesel can contain unsaturated fatty acids, which are susceptible to oxidation, being able to change into polymerized compounds. Oxidative stability is very important in the quality control of oils and biodiesel. In this study, biodiesel samples were produced through the methyl route, using a homogeneous catalyst. The determination of methyl esters was performed by gas chromatography in order to confirm the conversion of the carboxylic acids present in the raw material for the methyl esters. Also proved the presence of methyl linoleate and methyl oleate to the major constituent of biodiesel. The thermal and oxidative stability of sunflower and cotton oils and their biodiesel, using TG and P-DSC techniques were investigated. The use of P-DSC to measure the oxidative induction time was very important. These measurements were used to evaluate the cotton and sunflower oils, and their respective biodiesel. It was found that the thermal-oxidative stability of vegetable oils and their biodiesel were similar, due to the fact that both presented chemical composition and percentages of fatty acids similar.     

Monte Carlo Simulation of Ion Trajectories of Reacting Chemical Systems: Mobility of Small Water Clusters in Ion Mobility Spectrometry

For the comprehensive simulation of ion trajectories including reactive collisions at elevated pressure conditions, a chemical reaction simulation (RS) extension to the popular SIMION software package was developed, which is based on the Monte Carlo statistical approach. The RS extension is of particular interest to SIMION users who wish to simulate ion trajectories in collision dominated environments such as atmospheric pressure ion sources, ion guides (e.g., funnels, transfer multi poles), chemical reaction chambers (e.g., proton transfer tubes), and/or ion mobility analyzers. It is well known that ion molecule reaction rate constants frequently reach or exceed the collision limit obtained from kinetic gas theory. Thus with a typical dwell time of ions within the above mentioned devices in the ms range, chemical transformation reactions are likely to occur. In other words, individual ions change critical parameters such as mass, mobility, and chemical reactivity en passage to the analyzer, which naturally strongly affects their trajectories. The RS method simulates elementary reaction events of individual ions reflecting the behavior of a large ensemble by a representative set of simulated reacting particles. The simulation of the proton bound water cluster reactant ion peak (RIP) in ion mobility spectrometry (IMS) was chosen as a benchmark problem. For this purpose, the RIP was experimentally determined as a function of the background water concentration present in the IMS drift tube. It is shown that simulation and experimental data are in very good agreement, demonstrating the validity of the method.      

Molecular selective photocatalysis by TiO2/nanoporous silica core/shell particulates

The coating of TiO(2) particles (P25) by a nanoporous silica layer was conducted to impart molecular recognitive photocatalytic ability. TiO(2)/nanoporous silica core/shell particles with varied pore diameters of the shell were synthesized by the reaction of P25 with an aqueous mixture of tetraethoxysilane and alkyltrimethylammonium chloride with varied alkyl chain lengths, followed by calcination. The TEM and nitrogen adsorption/desorption isotherms of the products showed that a nanoporous silica shell with a thickness of ca. 2nm and controlled pore diameter (1.2, 1.6, and 2.7 nm) was deposited on the titania particle when surfactants with different alkyl chain lengths (C12, C16 and C22) were used. The water vapor adsorption/desorption isotherms of the core/shell particles revealed that a larger amount of water adsorbed on the core/shell particles when the pore diameter is larger. The (29)Si MAS NMR spectra of the core/shell particles showed that the amount of surface silanol groups was independent of the water vapor adsorption capacity of the products. The possible molecular recognitive photocatalysis on the products was investigated under UV irradiation using two kinds of aqueous mixtures containing different organic compounds with varied sizes and functional groups: a 4-butylphenol, 4-hexylphenol, and 4-nonylphenol mixture and a 2-nitrophenol, 2-nitro-4-phenylphenol, and 4-nitro-2,6-diphenylphenol mixture. It was found that the core/shell particles exhibited selective adsorption-driven molecular recognitive photocatalytic decomposition of 4-nonylphenol and 2-nitrophenol in the two mixtures.     

Liquid chromatographic separation of proteins derivatized with a fluorogenic reagent at cysteinyl residues on a non-porous column for differential proteomics analysis

A wide-pore (30 nm) reversed-phase column (Intrada WP-RP, particle size 3 μm) was recently utilized for protein separation in differential proteomics analysis with fluorogenic derivatization-liquid chromatography-tandem mass spectrometry (FD-LC-MS/MS), and exerted a tremendous effect on finding biomarkers (e.g., for breast cancer). Further high-performance separation is required for highly complex protein mixtures. A recently prepared non-porous small-particle reversed-phase column (Presto FF-C18, particle size: 2 μm) was expected to more effectively separate derivatized protein mixtures than the wide-pore column. A preliminary experiment demonstrated that the peak capacity of the former was threefold greater than that of the latter in gradient elution of a fluorogenic derivatized model peptide, calcitonin. The FD-LC-MS/MS method with a non-porous column was then optimized and applied to separate liver mitochondrial proteins that were not efficiently separated with the wide-pore column. As a result, high-performance separation of mitochondrial proteins was accomplished, and differential proteomics analysis of liver mitochondrial proteins in a hepatitis-infected mouse model was achieved using the FD-LC-MS/MS method with the non-porous column. This result suggests the non-porous small-particle column as a replacement for the wide-pore column for differential proteomics analysis in the FD-LC-MS/MS method.     

Gamma-ray spectroscopy of hypernuclei: Recent results and future plans

A series of hypernuclear γ-ray spectroscopy experiments using a germanium detector array, Hyperball, have accumulated precise data on various p-shell Λ hypernuclei. Recently, ¹²_ΛC and ¹¹_ΛB were studied at KEK using the (π⁺,K⁺γ) reaction, and a transition from a directly-populated spin-flip state, ¹⁶_ΛO(2⁻), was observed in BNL E930 data. It is discussed whether the spin-dependent ΛN interaction parameters determined from previous experiments can consistently explain other γ spectroscopy data. At the J-PARC facility, further hypernuclear γ-ray spectroscopy experiments are planned, particularly to measure the g factor of a Λ in a nucleus from a spin-flip B(M1) value and to investigate the ΛN interaction more in detail.