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71.
72.
Two novel lipopeptides, which have the peptide ligands [α-melanocyte stimulating hormone (α-MSH)] sequence and repeated [Gly-Arg-Gly-Asp-Se
(GRGDS) sequence[, are designed, synthesized by the solid-phase method, and introduced into liposome membranes by the freeze-thaw
method. These liposomes bearing the peptide ligands on their surface are expected to bind to cell membranes. We have confirmed
that the lipopeptides are introduced into liposome membranes almost quantitatively, while such a high degree of incorporation
has not been accomplished in conventional methods. In this respect, the present method is superior to prepare surface-modified
liposomes that are applicable to drug carriers and so on. We have also confirmed by using immunoelectron microscopy that the
peptide ligands are actually located in an aqueous phase. It has been shown by flow cytometry that the liposome bearing α-MSH
peptide ligand binds to B16 cells and the liposome bearing the repeated GRGDS sequence binds to NIH3T3 cells. 相似文献
73.
Hidekazu Tanaka Saki Nagano Tatsuo Ishikawa Takenori Nakayama 《Advanced Powder Technology》2019,30(4):807-814
In order to simulate the atmospheric corrosion of Zn-Al alloy coating on the steels in industrial zone, zinc hydroxysulfate (Zn4(OH)6(SO4)·nH2O: ZHS) rust was artificially synthesized by hydrolyzing the ZnO particles in a mixture of aqueous ZnSO4 and Al2(SO4)3 solutions and the structure and properties of the products were examined by various means. Then, the atomic ratio XAl?=?Al(III)/(Zn(II)?+?Al(III)) in the solution was ranged from 0 to 1.0. Adding Al(III) decreased the solution pH before aging to inhibit rust formation. Added Al(III) was easily incorporated in the particles than Zn(II). Increasing XAl turned the major rust following as hexagonal plate-like ZHS particles?→?hexagonal plate-like Zn-Al layered double hydroxide (LDH) particles?→?cubic Al6O5(SO4)4·H2O particles. These rust particles possessed a high adsorption affinity to corrosive CO2 gas. From these results, it can be supposed that atmospheric corrosion of Zn-Al alloy coating on the steels in industrial district produces the dense and compact rust layer composed of plate-like ZHS and/or Zn-Al-LDH particles owing to their preferred orientation to suppress further corrosion of steels. 相似文献
74.
Photo-degradable poly(vinyl chloride) (PVC)/titanium dioxide (TiO2) nanohybrid has been investigated to be utilized as an eco-friendly alternative strategy to the current waste landfill and toxic byproduct-emitting incineration of PVC wastes. Thus, the present study suggests a novel idea related to preparing the photocatalytically degradable nanohybrid through TiO2 nanoparticle-integrated hyperbranched poly(ε-caprolactone) (HPCL-TiO2). The main aim of this study is to find a solution to the unresolved problem in the conventional PVC/TiO2 composites related to the poor dispersion of the nanoparticles in PVC polymer. First, TiO2 nanoparticles are prepared by a sol-gel process, and the size of the particle is about 5-10 nm in diameter as measured by using a transmission electron microscopy (TEM) and dynamic light scattering (DLS). The hyperbranched poly(ε-caprolactone) (HPCL) with numerous COOH groups and good miscibility with PVC as a binder for TiO2 nanoparticles is prepared from moisture-sensitive catalyst-free polymerization of 2,2-bis[ω-hydroxy oligo(ε-caprolactone)methyl]propionic acids followed by modification reaction using pyridinium dichloromate (PDC), then characterized with 1H NMR and 13C NMR analyses. The integration of TiO2 nanoparticles onto HPCL is carried out by a dip-coating method based on the spontaneous self-assembly between TiO2 nanoparticles and HPCL, and the loading amount of the nanoparticles in the HPCL-TiO2 is determined to be ca. 3.3 wt% by X-ray photoelectron spectroscopy (XPS). Then, the HPCL-TiO2 is blended with PVC by solution blending in THF as solvent, and the resulting dispersibility of TiO2 nanoparticle in PVC is characterized by field emission scanning electron microscopy (FESEM) equipped with energy dispersive spectrometry (EDS), which exhibits the TiO2 nanoparticles are well-dispersed in PVC matrix, while some agglomerates are observed in the PVC/TiO2 sample prepared from TiO2 nanoparticle itself. The photocatalytic degradation of the samples are examined and verified from the change of surface morphology, chemical structure, molecular weight, and molecular-level structure after UV irradiation through field-emission scanning electron microscopy (FESEM), UV-visible spectroscopy, gel permeation chromatography (GPC), and positron annihilation lifetime spectroscopy (PALS). The remarkable photocatalytic degradation is observed in the PVC/HPCL-TiO2, and the structural change accompanied by the degradation of the irradiated sample can clearly explained. 相似文献
75.
Summary Ethylene polymerization was conducted with a catalyst prepared by mixing 2,6-bis{1-[2,6-(diisopropylphenyl)imino]ethyl}pyridine
iron dichloride, Mg(C2H5)(n-C4H9) and Al(C2H5)1.5Cl1.5 in the presence of common alkylaluminium as cocatalyst. Both the activity and the molecular weight of polymers produced were
markedly dependent upon the polymerization temperature. The end-group analysis of polymers showed that the molecular weight
of polymers produced at higher temperature was reduced by chain transfer with Al(C2H5)3 in addition to β-hydrogen elimination. 相似文献
76.
The specific surface area (SA) of the rusts formed by exposing various kinds of steels in different situations was determined by N2 adsorption. The SA values of the rusts increased with the increase of corrosion rate, implying that the rust layers with large SA exhibit a high resistance to corrosion. The suppression of rusting by compact rust layers was interpreted by the blockage of pores in rust layers by the adsorption and capillary condensation of water. The SA values clearly reflect the corrosion levels estimated by the external observation. It was convinced that the SA measurement is a universal quantitative technique to appraisal the protective function of rust layers. 相似文献
77.
This paper describes an atomic force microscope (AFM) based instrument for nanometer edge profile measurements of diamond cutting tools. The instrument is combined with an AFM unit and an optical sensor for alignment of the AFM probe tip with the top of the diamond cutting tool edge in the submicrometer range. In the optical sensor, a laser beam from a laser diode is focused to generate a small beam spot with a diameter of approximately 10 μm at the beam waist, and then received by a photodiode. The tool edge top and the AFM probe tip are brought to the center of the beam waist, respectively, through monitoring the variation of the photodiode output. To reduce the influence of the electronic noise on the photodiode output so that the positioning resolution can be improved, a modulation technique is employed that modulates the photodiode output to an AC signal by driving the laser diode with a sinusoidal current. Alignment experiments and edge profile measurements are carried out. 相似文献
78.
Takamasa Mori Yukari Hori Huang Fei Ikue Inamine Kazuki Asai Takayoshi Kiguchi JunIchiro Tsubaki 《Advanced Powder Technology》2012,23(5):661-666
In our previous paper we found that the particles in the slurry can agglomerate by adding larger amount of polyelectrolyte dispersant compared to that needed to attain well dispersion. Thus, the dependency of initial particle concentration on the agglomeration and its mechanism in slurry prepared by adding excess polyelectrolytes was experimentally discussed. It was shown that agglomeration behavior strongly depends on the additive amount of polyelectrolytes, not on the polyelectrolyte concentration in the solution. It was also found that the dominant factor of agglomeration in slurry prepared by adding extra polyelectrolytes should be the compression of the electrical double layer by the increased counter ion concentration, not by the so called depletion effect or by pH change. Interestingly, the final sediment had a relatively high packing fraction and good flowability in the case of the agglomerated slurry with extra polyelectrolytes compared to that of the agglomerated slurry with an additional NaCl solution. 相似文献
79.
Capacitive level meter for liquid hydrogen 总被引:1,自引:0,他引:1
Koichi Matsumoto Masamitsu Sobue Kai Asamoto Yuta Nishimura Satoshi Abe Takenori Numazawa 《低温学》2011,(2):114-115
A capacitive level meter working at low temperatures was made to use in magnetic refrigerator for hydrogen liquefaction. The liquid level was measured from the capacitance between parallel electrodes immersed in the liquid. The meter was tested for liquid nitrogen, hydrogen, and helium. The operation was successful using an AC capacitance bridge. The estimated sensitivity of the meter is better than 0.2 mm for liquid hydrogen. The meter also worked with pressurized hydrogen. 相似文献
80.