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11.
Sn-incorporated folded sheets mesoporous materials (Sn-FSM-16) with various contents of Sn were synthesized by using a mixture of water glass, SnCl4 and NaOH as starting materials. Hexadecyltrimethyl-ammonium chloride (surfactant) was used to intercalate into the layered silicate. The reaction process was followed by measurements of XRD patterns of intermediates. The Sn-FSM-16 was formed via the following mechanism: (1) layered silicates such as - - and -Na2Si2O5 were formed as intermediates by the calcination of the mixture of the starting materials; (2) the surfactant was intercalated into the layered silicates; (3) the surfactant-silicate complex with hexagonal structure was obtained as a precursor of Sn-FSM-16; (4) the precursor was calcined to decompose the surfactant in the interlayer and was changed to Sn-FSM-16. The structural aspect of Sn in Sn-FSM-16 was studied by XPS profiles of Sn 3d
5/2 and Si2p, 29 Si MAS NMR and FTIR. The content of Sn in Sn-FSM increased with increasing concentrations of both Sn and NaOH in the starting materials. The surface area of Sn-FSM-16 decreased with an increase of Sn content in Sn-FSM (1160–620 m2/g). 相似文献
12.
Hiroaki Tsuchiya Jan M. Macak Andrei Ghicov Luciano Taveira Patrik Schmuki 《Corrosion Science》2005,47(12):3324-3335
The present work investigates the electrochemical formation of self-organized high aspect ratio TiO2 and ZrO2 nanotube layers. The formation and growth of a self-organized porous layer can be achieved directly by anodization without any templates in fluoride containing electrolytes. The morphology of the porous layers is affected by the electrochemical conditions such as the electrolyte composition, the pH and the exact polarization treatment (such as the potential sweep rate from the open-circuit potential to the anodizing potential). For Ti, nanotube layers are formed with diameters varying from approx. 20 nm to 100 nm and lengths from approx. 0.25 μm to 2.5 μm depending on the electrolytes and pH. On the other hand, for Zr, tubes of 50 nm in diameter and up to approx. 17 μm in length can be grown—a key parameter in this case is the potential sweep rate. The large difference between Ti and Zr in the achievable thickness of nanotube layers indicates a difference in the growth mechanism which may be based on the different chemical dissolution rates of electrochemically formed oxides. 相似文献
13.
Template‐Free Fabrication of Mesoporous Alumina Nanospheres Using Post‐Synthesis Water‐Ethanol Treatment of Monodispersed Aluminium Glycerate Nanospheres for Molybdenum Adsorption
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Indra Saptiama Yusuf Valentino Kaneti Yoshitaka Suzuki Kunihiko Tsuchiya Nobuyoshi Fukumitsu Takeji Sakae Jeonghun Kim Yong‐Mook Kang Katsuhiko Ariga Yusuke Yamauchi 《Small (Weinheim an der Bergstrasse, Germany)》2018,14(21)
This work reports the template‐free fabrication of mesoporous Al2O3 nanospheres with greatly enhanced textural characteristics through a newly developed post‐synthesis “water‐ethanol” treatment of aluminium glycerate nanospheres followed by high temperature calcination. The proposed “water‐ethanol” treatment is highly advantageous as the resulting mesoporous Al2O3 nanospheres exhibit 2–4 times higher surface area (up to 251 m2 g?1), narrower pore size distribution, and significantly lower crystallization temperature than those obtained without any post‐synthesis treatment. To demonstrate the generality of the proposed strategy, a nearly identical post‐synthesis “water treatment” method is successfully used to prepare mesoporous monometallic (e.g., manganese oxide (MnO2)) and bimetallic oxide (e.g., CuCo2O4 and MnCo2O4) nanospheres assembled of nanosheets or nanoplates with highly enhanced textural characteristics from the corresponding monometallic and bimetallic glycerate nanospheres, respectively. When evaluated as molybdenum (Mo) adsorbents for potential use in molybdenum‐99/technetium‐99m (99Mo/99mTc) generators, the treated mesoporous Al2O3 nanospheres display higher molybdenum adsorption performance than non‐treated Al2O3 nanospheres and commercial Al2O3, thereby suggesting the effectiveness of the proposed strategy for improving the functional performance of oxide materials. It is expected that the proposed method can be utilized to prepare other mesoporous metal oxides with enhanced textural characteristics and functional performance. 相似文献
14.
Yusuke Fukui Yosuke Honda Yasuhiro Yamauchi Michiko Okafuji Masahiro Sakai Mikihiko Nishitani Yusuke Takata 《Journal of the Society for Information Display》2010,18(12):1090-1094
Abstract— MgO thin film is currently used as a surface protective layer for dielectric materials because MgO has a high resistance during ion sputtering and exhibits effective secondary electron emission. The secondary‐electron‐emission coefficient γ of MgO is high for Ne ions; however, it is low for Xe ions. The Xe content of the discharge gas of PDPs needs to be raised in order to increase the luminous efficiency. Thus, the development of high‐γ materials replacing MgO is required. The discharge properties and chemical surface stability of SrO containing Zr (SrZrO) as the candidate high‐γ protective layer for noble PDPs have been characterized. SrZrO films have superior chemical stability, especially the resistance to carbonation because of the existence of a few adsorption sites due to their amorphous structure. The firing voltage is 60 V lower than that of MgO films for a discharge gas of Ne/Xe = 85/15 at 60 kPa. 相似文献
15.
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17.
Tsuchiya T. Nagano S. Paidi R.B. Kikuno T. 《Parallel and Distributed Systems, IEEE Transactions on》2001,12(1):81-95
A distributed system is said to be self-stabilizing if it converges to safe states regardless of its initial state. In this paper we present our results of using symbolic model checking to verify distributed algorithms against the self-stabilizing property. In general, the most difficult problem with model checking is state explosion; it is especially serious in verifying the self-stabilizing property, since it requires the examination of all possible initial states. So far applying model checking to self-stabilizing algorithms has not been successful due to the problem of state explosion. In order to overcome this difficulty, we propose to use symbolic model checking for this purpose. Symbolic model checking is a verification method which uses Ordered Binary Decision Diagrams (OBDDs) to compactly represent state spaces. Unlike other model checking techniques, this method has the advantage that most of its computations do not depend on the initial states. We show how to verify the correctness of algorithms by means of SMV, a well-known symbolic model checker. By applying the proposed approach to several algorithms in the literature, we demonstrate empirically that the state spaces of self-stabilizing algorithms can be represented by OBDDs very efficiently. Through these case studies, we also demonstrate the usefulness of the proposed approach in detecting errors 相似文献
18.
Quick-freeze deep-etch replica electron microscopy gives high contrast snapshots of individual protein molecules under physiological conditions in vitro or in situ. The images show delicate internal pattern, possibly reflecting the rotary-shadowed surface profile of the molecule. As a step to build the new system for the "Structural analysis of single molecules", we propose a procedure to quantitatively characterize the structural property of individual molecules; e.g. conformational type and precise view-angle of the molecules, if the crystallographic structure of the target molecule is available. This paper presents a framework to determine the observed face of the protein molecule by analyzing the surface profile of individual molecules visualized in freeze-replica specimens. A comprehensive set of rotary-shadowed views of the protein molecule was artificially generated from the available atomic coordinates using light-rendering software. Exploiting new mathematical morphology-based image filter, characteristic features were extracted from each image and stored as template. Similar features were extracted from the true replica image and the most likely projection angle and the conformation of the observed particle were determined by quantitative comparison with a set of archived images. The performance and the robustness of the procedure were examined with myosin head structure in defined configuration for actual application. 相似文献
19.
A case of bilateral hypernephroma treated by right heminephrectomy in situ and "benchwork" excision of two tumors from the left kidney followed by autotransplantation is presented. Follow-up examination has demonstrated good renal function with no evidence of tumor recurrence or metastasis. This case illustrates the feasibility of benchwork operation and its application to renal tumors, particularly when these tumors are bilateral and preservation of renal tissue is imperative. Long-term follow-up of patients managed by this technique is mandatory. 相似文献
20.
K. Daoudi T. Tsuchiya I. Yamaguchi T. Manabe S. Mizuta T. Kumagai 《Journal of Electroceramics》2006,16(4):527-532
Epitaxial La0.7Ca0.3MnO3 (LCMO) thin films were successfully prepared by the metal-organic deposition process on various (001) single-crystal substrates:
MgO, LaAlO3 (LAO), SrTiO3 (STO), and (LaAlO3)0.3-(SrAlTaO6)0.7 (LSAT). The crystallinity and the epitaxial growth of the LCMO films were characterized by X-ray diffraction (θ − 2θ scans
and pole-figure analysis). The temperature dependence of the resistance of the LCMO/LSAT, LCMO/STO and LCMO/LAO films exhibit
typical characteristics with a transition from the paramagnetic-insulator state to the ferromagnetic-metallic state at a temperature
peak (T
p
) ranging from 258 to 270 K. However, the LCMO/MgO films exhibited a semiconducting behavior without any transition. Based
on the R(T) measurement, we calculated the temperature coefficient of resistance (TCR) for a bolometric application and we obtained
22%/K, 10.2%/K and 27.5%/K for the film grown on the LSAT, STO and LAO substrates, respectively. This difference in the TCR
properties is related to the strain induced by the lattice mismatch between LCMO and the different substrates. 相似文献