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1.
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The formation of mixed ligand complexes in Ti(IV)-xylenol orange (XO)-H2O2 and Ti(IV)-chromazurol S (CAS)-H2O2 systems was studied by spectrophotometry. The former system gave constant absorbance (λmax = 562 nm) under the condition of [XO]/[Ti(IV)] = 1 in the pH 2–4 region. In the latter system, a distinct maximum at 557 nm was observed when [CAS]/[Ti(IV)] = 4 in the pH range of 4.5–5.2. In both cases, the absorbance at λmax was stable for a long time and proportional to the concentration of hydrogen peroxide. From those facts, the usefulness of the mixtures of Ti(IV)-XO and Ti(IV)-CAS as the colorimetric reagents for the determination of hydrogen peroxide can be expected. The conditions for the use of the Ti(IV)-XO and the Ti(IV)-CAS reagents were examined in detail, and both reagents were found to be available for trace analysis of hydrogen peroxide with high sensitivity. 相似文献
3.
The catalytic oxidation of glucose on Pt electrodes modified by adsorbed metals was studied in 1 M HClO4 by linear sweep voltammetry. The adsorbed metals (denoted as Mad, such as Biad and Pbad) formed on Pt in the potential region more positive than the reversible potential of an M=+/Mo couple, lead to a marked increase in the anodic c?urrent of glucose by about one order of magnitude. The catalytic activity depends on the surface coverage by the Mad. The strongly adsorbed species of lactone type, which are responsible for blocking the successive oxidation, are formed on the electrode surface in the anodic processes of glucose on a bare Pt electrode. The formation of such poisonous species is accelerated in the presence of adsorbed hydrogen on Pt. The effects of Mad were discussed on the basis that Mad plays its major role on the Pt electrode surface in removal of the adsorbed hydrogen which initiates the formation of the poisonous species. 相似文献
4.
S. Takamura 《辐射效应与固体损伤》2013,168(4):115-118
Temperature dependence of yield stress was studied on Mo single crystals of two orientations after neutron irradiation at low temperature. After the low temperature irradiation, the yield stresses decreased. The isochronal annealing measurements of yield stress were also performed. The yield stresses after low temperature irradiation recovered with increasing of annealing temperature. 相似文献
5.
Naofumi Nishida Yuki Hori Akane Yamauchi Hazuki Fujiwara Makoto Sakurai Yuya Fujiwara Shin-ichi Honda Shunjiro Fujii Hiroyuki A. Sakaue Daiji Kato Tomohiro Yamaguchi Koji Ishibashi Toshifumi Terui Kuei-Yi Lee 《X射线光谱测定》2020,49(1):99-103
Interaction of highly charged ions (HCIs) with surfaces produce various specific phenomena as a consequence of the potential energy that HCI possesses. In the present study, we have observed photon emission, structural, magnetic, and electronic modification on various carbon-based materials such as carbon nanotube by the impact of HCIs using an electron beam ion source named Kobe EBIS installed at the Kobe University. In order to study the potential effect, HCIs of Arq+ (q = 6–16) with the intensity of 0.1–1 nA are projected on the surface with a constant kinetic energy (16 keV). For photon emission measurements, we observed spatial and spectral distribution of visible light emission from the surface during irradiation with HCIs. On the other hand, the structural modification of multi-walled carbon nanotubes (MWCNTs) irradiated with HCIs has been analyzed using a transmission electron microscopy and Raman spectroscopy. Irradiation effects on the resistivity of single MWCNT supported on micrometer scale bridge pattern were also measured. We have also measured magnetic structure of highly oriented pyrolytic graphite irradiated with HCIs using electron spin resonance at low temperature. At the present paper, we will review our recent experimental results on the interaction of HCI with various carbon-based materials. 相似文献
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The high-pressure effects on lithium ion conduction in LiBH4 have been investigated. The high-pressure ac-impedance measurement was performed by using a cubic anvil-type apparatus under 2 to 6 GPa at various temperatures. For the hexagonal structure (Phase I), the activation volume for lithium ion conduction was found to be around 3 cm3/mol (≈ 0.09Vm, where Vm means its molar volume). This activation volume is almost comparable to that for other fast-ion conductors such as NASICONs. The lithium ion conductivities of orthorhombic (Phase III) and cubic (Phase V) structures were also measured. Regardless of crystal structures, the activation energies of Phases I, III, and V were almost identical at around 50 to 60 kJ/mol; on the other hand, the pre-exponential terms of Phases III and V were smaller than those of Phase I by one to two orders of magnitude. 相似文献
8.
To find the pairs of fluorogenic reagents having similar retention times in HPLC but with different fluorescent characteristics, six fluorogenic reagents bearing benzoxadiazole or benzoselenadiazole skeletons were synthesized. The resultant derivatives obtained from the reaction of peptides and proteins with reagents which have a benzoselenadiazole skeleton showed different fluorescence characteristics from those with a benzoxadiazole skeleton. Since each corresponding derivatives of trypsin inhibitor and BSA with DAABD-Cl and 7-fluoro-N-[2-(diethylamino)ethyl]-2,1,3-benzoselenadiazole-4-sulfonamide (DEAEABSeD-F) have similar retention times, the pair of reagents was adopted for the sensitive simultaneous detection of proteins in two different samples. When the soluble fraction of mouse hippocampus was divided into the two samples (A and B), each was reacted with DEAEABSeD-F for A and DAABD-Cl for B, respectively. The two reaction solutions were combined and subjected to HPLC analysis with two fluorescent detectors in series (excitation and emission at different wavelengths for A and B, respectively). The resultant two chromatograms had quite similar patterns for each other. The new pair of fluorogenic reagents (DAABD-Cl and DEAEABSeD-F) would be applicable to proteomics studies using the previously reported FD-LC-MS/MS method. 相似文献
9.
Hiroyoshi Takamura Yuichiro Kadonaga Chunguang Han Daisuke Uemura 《Tetrahedron》2009,65(36):7449-7725
Cross-metathesis of methyl ester which was prepared from symbiodinolide with ethylene was performed to give the C33-C42 degraded fragment. This fragment was estimated to be (36S,40S)-diol by the modified Mosher method. Stereoselective synthesis of the (36S,40S)-diol and its diastereomer (36R,40S)-diol was achieved from l-aspartic acid. Synthetic bis-(S)- and (R)-MTPA esters which were derivatized from the (36S,40S)-diol exhibited spectroscopic data identical with those of bis-(S)- and (R)-MTPA esters derived from the degraded product. Thus, the absolute stereochemistry of the C33-C42 fragment was elucidated to be (36S,40S). 相似文献
10.
Andreas Meissner Takayuki Kishi Yuka Fujisawa Yuto Murai Hiroyoshi Takamura Isao Kadota 《Tetrahedron letters》2018,59(51):4492-4495
A stereoselective formal total synthesis of enigmazole A, a marine macrolide isolated from Cinachyrella enigmatica, is described. Lewis acid mediated intramolecular allylation of an α-acetoxy ether, prepared from alcohol and carboxylic acid fragments was carried out to construct the methylene THP ring with high stereoselectivity. The late-stage macrolactonization of the corresponding seco-acid provided a known synthetic intermediate of enigmazole A. 相似文献