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151.
M. Ali HaiderAaron J. Capizzi Mitsuhiro MurayamaSteven McIntosh 《Solid State Ionics》2011,196(1):65-72
La0.6Sr0.4CoxFe1−xO3−δ (LSCF), La0.6Sr0.4Cu0.2Fe0.8O3−δ, Ba0.5Sr0.4Co0.8Fe0.2O3−δ and LaFeO3−δ nanoparticles were synthesized by a reverse micelle procedure. Controlling the size of the micelles through the water:oil phase ratio enabled synthesis of phase pure perovskite particles with average sizes from 14 nm to 50 nm. Small amounts of an impurity phase, likely cobalt oxide, were detected in the XRD spectrum of high cobalt content samples of LSCF (x = 0.8). La0.6Sr0.4Co0.2Fe0.8O3−δ nanoparticles were utilized to coat the surface of a dense thin-film La0.6Sr0.4Co0.2Fe0.8O3−δ solid oxide fuel cell cathode. The polarization resistance of the nanoparticle coated electrode, measured at open circuit in air at 973 K, was 20% lower than an equivalent un-coated electrode. 相似文献
152.
Akira Zenidaka Toshiyuki Honda Mitsuhiro Terakawa 《Applied Physics A: Materials Science & Processing》2011,105(2):393-398
We describe the physics of the SERS based on the optical near-field intensity enhancement on the metallic (plasmonic) and
the nonmetallic (Mie scattering) nanostructured substrates with two-dimensional (2D) periodic nanohole arrays. The calculation
by the Finite-Difference Time-Domain (FDTD) method revealed that the optical intensity enhancement increases with the increase
of the thickness of a gold film coating on the nonmetallic (dielectric) nanostructured Si, GaAs, and SiC substrates. The resonance
spectrum shifts with the changes in the geometrical structure of the void diameter and inter-void distance. It was clarified
that the optical intensity enhancement obtained with the gold-coated substrate is equivalent to that with a gold substrate
at 70-nm thick gold coating on the dielectric substrates in this structure. The resonance spectral bandwidth for Mie scattering
and plasmonic near-fields is different. Therefore, if the Stokes line of the Raman scattering is located within the resonance
bandwidth, the SERS signal is enhanced proportionally to the fourth power of the electric near-field. However, if the Stokes
shift is located out of the resonance bandwidth, the SERS signal enhancement is only proportional to the square of the scattered
near-field. 相似文献
153.
Tetsutaro Shibata 《Mathematische Nachrichten》2016,289(14-15):1934-1945
We consider the equation which is called Holling–Tanner population model where is a bifurcation parameter and are unknown constants. In this paper, we determine the unknown constants from the asymptotic behavior of the bifurcation curve , where . 相似文献
154.
In order to clarify the suitability of 198Au-colloid and Na251CrO4 as a marker of transit of the gastrointestinal content of the chicken, the distribution, absorption and excretion of 198Au-colloid and Na251CrO4 in the chicken were examined. Orally administered 198Au-colloid was not absorbed by the gastrointestinal tract and excreted into feces. Intravenously injected 198Au-colloid was not excreted into the gastrointestinal tract through the gastrointestinal wall. On the other hand, orally administered Na251CrO4 was relatively well absorbed by the gastrointestinal tract and distributed over a whole body. Intravenously injected Na251CrO4 was excreted into the gastrointestinal tract through the gastrointestinal wall and bile ducts. It seemed that 198Au-colloid was not adhered to the gastrointestinal mucosa and consequently, the transport of 198Au-colloid in the gastrointestinal tract was not delayed. It is concluded that 198Au-colloid is highly suitable as a marker of gastrointestinal transit of the chicken but Na251CrO4 is unsuitable. 相似文献
155.
A simple, reliable, trace determination of selenomethionine (Semet) based on a direct hydride generation atomic absorption spectrometric method was developed using sodium tetrahydroborate (0.3% in 0.2% NaOH) and hydrochloric acid (3 M). The method excluded any chemical pretreatment prior to hydride generation (HG). The optimized HG system was successfully coupled with the HPLC system. The detection limit (3σ of blank; n=5), reproducibility (R.S.D. of three successive analyses/day, performed on three different days), and repeatability (R.S.D. of three successive analyses) of the method were 1.08 ng ml−1, 9.8% for 9.04 ng ml−1 and 2.1–9.5% for 30.0–1.27 ng ml−1 Semet as Se (standards prepared in Milli-Q water). Calibration graph was linear up to 30 ng ml−1. This HPLC-HG-AAS method is very promising and successfully determined Semet (spiked) in human urine. 相似文献
156.
Amal Kaddoumi Mitsuhiro Wada Kenichiro Nakashima 《Biomedical chromatography : BMC》2011,25(5):579-587
N‐Nitrosofenfluramine (N‐Fen), a synthetic adulterant in Chinese herbal diet products, is believed to cause hepatotoxicity in people who use these products. N‐Fen is a relatively new compound, and thus pharmacological and toxicological studies are insufficient. The aim of this work was to (1) define N‐Fen's plasma pharmacokinetics and tissue distribution after single intraperitoneal (i.p.) administration of 25 mg/kg to rats; (2) define its bioavailability; and (3) identify fenfluramine (Fen) and norfenfluramine (Norf) as N‐Fen metabolites. N‐Fen rapidly appeared in the circulation and was distributed to all tissues. Norf was found to be the primary metabolite and not Fen. Plasma and tissue levels of N‐Fen and Norf were low with bioavailability of N‐Fen after i.p. administration was <3%. The AUC0−t of N‐Fen in the liver and kidney were 6.6 and 12.1 times, respectively, greater than the brain, and 17.8 and 32.6 times, respectively, greater than the plasma. In conclusion, N‐Fen did not show local accumulation in the liver, the site of toxicity, with concentrations represented as percentage of the total dose ranginng from 0.008 to 0.122%; hence the cause of hepatotoxicity could be related to the mechanisms other than toxicity consequences accumulation. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
157.
158.
159.
Mitsuhiro Hirata Yutaka Abe Bungo Ochiai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2010,48(20):4385-4392
Various star‐shaped poly(phenoxy propylene sulfide)s (PPSs) bearing curable end groups were synthesized by the functionalization of the propagating ends of star‐shaped poly(PPS) with various electrophilies. The functionalization with chloromethyl styrene proceeded quantitatively, and afforded polymers with Mn almost agreed with theoretical value and narrow Mw/Mn. The photocuring conditions were optimized, and the addition of 10 wt % of poly(ethylene glycol) diacrylate was effective to attain sufficient crosslinking. The photocuring reaction of the end‐functionalized poly(PPS) films cast on silicon wafers was conducted by UV irradiation. The cured poly (PPS)s became insoluble in THF, supporting the sufficient crosslinking. Developing of a cured polymer yielded a negative photoresist pattern. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
160.