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91.
Masahito Tagawa Kumiko Yokota Koji Matsumoto Yuden Teraoka Masahito Niibe 《Applied Surface Science》2010,256(24):7678-7683
Surface structural changes of a hydrogenated diamond-like carbon (DLC) film exposed to a hyperthermal atomic oxygen beam were investigated by Rutherford backscattering spectroscopy (RBS), synchrotron radiation photoelectron spectroscopy (SR-PES), and near-edge X-ray absorption fine structure (NEXAFS). It was confirmed that the DLC surface was oxidized and etched by high-energy collisions of atomic oxygen. RBS and real-time mass-loss data showed a linear relationship between etching and atomic oxygen fluence. SR-PES data suggested that the oxide layer was restricted to the topmost surface of the DLC film. NEXAFS data were interpreted to mean that the sp2 structure at the DLC surface was selectively etched by collisions with hyperthermal atomic oxygen, and an sp3-rich region remained at the topmost DLC surface. The formation of an sp3-rich layer at the DLC surface led to surface roughening and a reduced erosion yield relative to the pristine DLC surface. 相似文献
92.
We perform a Wilsonian renormalization group analysis for the nucleon–nucleon scattering in the P waves in the nuclear effective field theory including pions, in a similar way to the one done for the S-waves in our previous paper. We emphasize that the one-pion exchange interaction with large momentum transfer is of the same order as the leading contact interaction, so that there is no mismatch of the power counting. It is explicitly shown by obtaining consistent sets of renormalization group equations, that the cutoff dependence generated by the loop diagrams containing pion exchanges can be compensated by the cutoff dependence of the coupling constants of the contact interactions. 相似文献
93.
The generation and recognition of a record-length 511-chip optical code is experimentally demonstrated by use of a superstructured fiber Bragg grating (SSFBG) with a chip rate of 640 Gchips/s. Very high reflectivity (92%) is achieved with high-quality correlation properties. The temperature deviation tolerance is approximately +/- 0.3 degrees C, which is within the package's temperature stability range (+/- 0.1 degrees C). Experimental results show good agreement with the theory. They indicate the SSFBG's potential for processing a long optical code with an ultrahigh chip rate, which could significantly improve the system's performance. 相似文献
94.
In the anomaly-mediated supersymmetry (SUSY) breaking scenario, neutral gaugino of SUL(2) multiplet, Wino, can be the lightest SUSY particle and become a candidate for dark matter. We calculated scattering cross section of Wino dark matter with nucleon, which is responsible for direct detection of the dark matter, on the assumption that the SUSY particles and the heavier Higgs bosons have masses of the order of the gravitino mass in the SUSY standard model. In such a case, the Wino–nucleon coupling is generated by loop processes. We have included two-loop contribution to Wino–gluon interaction in the calculation, since it is one of the leading contributions to the Wino–nucleon coupling. It was found that the spin-independent scattering cross section with proton is 10−(46–48) cm2. While it is almost independent of the Wino mass, the result is quite sensitive to the Higgs boson mass due to the accidental cancellation. 相似文献
95.
Nobuaki Negishi Koji Takeuchi Takashi Ibusuki 《Journal of Sol-Gel Science and Technology》1998,13(1-3):691-694
Titanium dioxide (TiO2) coated glass-plate thin film photocatalysts for elimination of air pollutants, were prepared by the dip-coating process with titanium alkoxide including polyethylene glycol (PEG). The surface structure of these thin films changed drastically with the size of the PEG. They were either transparent or opaque. Nitrogen oxides (NOx), one of the most hazardous of air pollutants, were found to be efficiently eliminated by the thin film photocatalyst. The photocatalytic activities of the transparent and opaque thin films were found to be almost equal. This may be due to the two films having the same surface area. The highest activity was obtained for thin films around 1 m. 相似文献
96.
Kodera M Shimakoshi H Nishimura M Okawa H Iijima S Kano K 《Inorganic chemistry》1996,35(17):4967-4973
A mononucleating tripyridine ligand, 2-(bis(2-pyridyl)methyl)-6-methylpyridine (L(1)), and a dinucleating hexapyridine ligand, 1,2-bis[2-(bis(2-pyridyl)methyl)-6-pyridyl]ethane (L(2)), have been prepared. The reaction of a carbanion of 2,6-lutidine with 2-bromopyridine affords L(1) which is converted to L(2) quantitatively by treating with tert-butyllithium and 1,2-dibromoethane. (&mgr;-Oxo)bis(&mgr;-acetato)diiron(III) complexes [Fe(2)(O)(OAc)(2)(L(1))(2)](ClO(4))(2) (1) and [Fe(2)(O)(OAc)(2)L(2)](ClO(4))(2) (2) have been synthesized and characterized by means of infrared, UV/vis, mass, and M?ssbauer spectroscopies and by measuring magnetic susceptibility and cyclic voltammograms. All the spectral data are consistent with the (&mgr;-oxo)bis(&mgr;-acetato)diiron(III) core structure in both 1 and 2. A relatively strong molecular ion peak at m/z 865 corresponding to [{Fe(2)O(OAc)(2)L(2)}(ClO(4))](+) in a FAB mass spectrum of 2 suggests the stabilization of the (&mgr;-oxo)bis(&mgr;-acetato)diiron(III) core structure by L(2) in a solution state. The compound 2.DMF.2-PrOH.H(2)O, chemical formula C(44)Cl(2)Fe(2)H(51)N(7)O(16), crystallizes in the monoclinic space group C2/c with a = 22.034(6) ?, b = 12.595(5) ?, c = 20.651(7) ?, beta = 121.49(2) degrees, and Z = 4. The cation has 2-fold symmetry with the bridging oxygen atom on the 2-fold axis: Fe-(&mgr;-O) = 1.782(5) ?, Fe-O-Fe = 123.6(6) degrees, and Fe.Fe = 3.142(3) ?. The diiron(III) core structure of 2 seems to be stabilized by encapsulation of the ligand. Compound 2 is the first example of a discrete (&mgr;-oxo)bis(&mgr;-acetato)diiron(III) complex with a dinucleating ligand. 相似文献
97.
Reiko Saito Akifumi Fujita Ayako Ichimura Koji Ishizu 《Journal of polymer science. Part A, Polymer chemistry》2000,38(11):2091-2097
Novel structural microspheres of the Janus type, with microphase‐separated polystyrene (PS) and poly(tert‐butyl methacrylate) (PBMA) shells and crosslinked poly(2‐vinyl pyridine) (PVP) cores, were synthesized with the crosslinking of PVP spherical domains in poly(styrene‐block‐2‐vinyl pyridine‐block‐tert‐butyl methacrylate) ABC triblock terpolymer film with PS/PBMA lamellae–PVP spherical structures. For the formation of lamellae‐sphere structures, toluene, which was a selective solvent for the ABC triblock terpolymer, was used. With the crosslinking of PVP spheres in the microphase‐separated film with 1,4‐diiodobutane gas, the microphase structure of the terpolymer was fixed, and microspheres composed of microphase‐separated PS and PBMA shells and P2VP cores were obtained. The size distribution of the purified microspheres was narrow. The characteristics of the microspheres and their aggregation behaviors in selective solvents were investigated by transmission electron microscopy and light scattering methods. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 2091–2097, 2000 相似文献
98.
Koji Ishizu Daisuke Takahashi Hisashi Takeda 《Macromolecular rapid communications》2000,21(10):660-664
Two poly(4‐methylstyrene) (P4MS)‐block‐polystyrene (PS)‐block‐P4MS triblock copolymers were prepared by successive anionic addition of styrene and 4‐methylstyrene monomers as the core backbone ( CB ) for the architecture of block‐graft polymers. Both terminal 4‐methylstyrene blocks of CB were metalated with a sec‐butyllithium (sec‐BuLi)/tetramethylethylenediamine (TMEDA) complex in cyclohexane. The first‐generation block‐graft polymer ( 1BG ) was prepared by anionic polymerization of α‐methylstyrene by the lithiated CB in tetrahydrofuran (THF) at –78°C and subsequently the terminal graft ends were capped with a small amount of 4‐methylstyrene. The characterization of those block‐graft polymers was carried out in detail. 相似文献
99.
We showed previously that poly(L-lactide)-grafted dextran could form biodegradable nanogels in water. In this paper, various properties of Dex-g-PLLA nanogels were compared with Dex-Chol (dextran-cholesterol conjugate) nanogels to investigate the effects of hydrophobic units. Dex-g-PLLA nanogels exhibited significantly lower CAC and higher colloidal stability, indicating a strong tendency to form nanogels. We prepared lysozyme-loaded Dex-g-PLLA nanogels, and they exhibited a sustained release of lysozyme for 1 week without denaturation in PBS at 37 degrees C. The Dex-g-PLLA nanogels therefore have great potential as a delivery vehicle for therapeutic protein. 相似文献
100.
Suzuki M Husimi Y Komatsu H Suzuki K Douglas KT 《Journal of the American Chemical Society》2008,130(17):5720-5725
Fluorescent acceptors have been immobilized on nanoparticulate quantum dots (QDs), which serve in turn as their FRET donors. The broad excitation and narrow emission bands of QDs mark them as having excellent potential as donors for FRET and, in principle, differently colored QDs could be excited simultaneously. The present work describes the preparation and operation of FRET-based QD bioprobes individually able to detect the actions of protease, deoxyribonuclease, DNA polymerase, or changes in pH. In addition, two such QD-mounted biosensors were excited at a single wavelength, and shown to operate simultaneously and independently of each other in the same sample solution, allowing multiplex detection of the action of a protease, trypsin, in the presence of deoxyribonuclease. 相似文献