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排序方式: 共有305条查询结果,搜索用时 15 毫秒
1.
Kazuo Yamana Masayasu Tokonami Kohji Nobugai Nobuo Morimoto† Mitsue Koizumi Isamu Shindo 《Journal of the American Ceramic Society》1981,64(3):43-c-
A birefringence of siliceous glass, which is coexisting with mullite crystals, was studied by an optical polarizing microscope. The cause of the birefringence was assumed to be the residual stress induced by a large contraction difference between the mullite and glass on cooling. The stress has been evaluated to be as high as—0.3 GPa, and to correspond to the elastic one which began to develop at the glass transition point. 相似文献
2.
Masatomo Yashima Katsuya Ohtake Masato Kakihana Masahiro Yoshimura 《Journal of the American Ceramic Society》1994,77(10):2773-2776
Homogeneous metastable tetragonal ( t ') solid solutions of ZrO2 — x mol% CeO2 ( x = 20 and 50) were successfully synthesized by the organic polymerized complex method. The citric acid-ethylene glycol solution containing Zr and Ce ions was polymerized at about 140°C and then heat-treated at about 350°C to obtain a precursor. The black precursor was heated at 450°C and then fired up to 1300° or 1590°C, resulting in the homogeneous solid solutions. 相似文献
3.
Meso-porous Al2O3-supported Ni catalysts exhibited the highest activity, stability and excellent coke-resistance ability for CH4 reforming with CO2 among several oxide-supported Ni catalysts (meso-porous Al2O3 (Yas1-2, Yas3-8), -Al2O3, -Al2O3, SiO2, MgO, La2O3, CeO2 and ZrO2). The properties of deposited carbons depended on the properties of the supports, and on the meso-porous Al2O3-supported Ni catalyst, only the intermediate carbon of the reforming reaction formed. XRD and H2-TPR analysis found that mainly spinel NiAl2O4 formed in meso-porous Al2O3 and -Al2O3-supported catalysts, while only NiO was detected in -Al2O3, SiO2, CeO2, La2O3 and ZrO2 supports. The strong interaction between Ni and meso-porous Al2O3 improved the dispersion of Ni, retarded its sintering and improved the activated adsorption of CO2. The coking reaction via CH4 temperature-programed decomposition indicated that meso-porous Al2O3-supported Ni catalysts were less active for carbon formation by CH4 decomposition than Ni/-Al2O3 and Ni/-Al2O3. 相似文献
4.
Minoru Tsuda Setsuko Oikawa Akira Yokota Mitsuo Yabuta Wataru Kanai Ken-Ichi Kashiwagi Isamu Hijikata Hisashi Nakane 《Polymer Engineering and Science》1983,23(18):993-999
A dry developable negative working resist composition comprised of poly(methyl isopropenyl ketone) (PMIPK) and 4-methyl-2,6-di(4′-azido-benzylidene) cyclohexanone-1 was examined. The main photochemical product formed in the resist pattern was found to be a secondary amine which crosslinks PMIPK. Post-annealing forms a hydrogen-bonded product which shows a powerful electronic excitation energy quenching effect. The quencher is more powerful than the aromatic compound arising from the azide by post-annealing only. The residual resist thickness of the negative pattern is about 80 percent of the initial thickness of the coating in spite of all the azide compound remaining in the resist coating. The obtained dry developed resist pattern has a high dry etch resistance. Etchings of Si and SiO2 were performed by plasma and reactive ion etching, respectively. 相似文献
5.
Three samples of LaCoO3 were prepared by two different methods and calcined at 800 or 1000 °C. They had BET areas of 1, 12, and 16 m2/g and all of them showed pure perovskite X-ray diffraction patterns with identical unit cell dimensions. In a series of experiments the oxide, having larger surface area, was stepwise reduced in hydrogen at temperatures between 60 and 500 °C. The XPS spectra, taken at room temperature after evacuation at 400 °C at each reduction level, showed that the surface concentration of Co° was very low up to 300 °C but increased sharply between 300 and 350 °C (9–75%). This concentration further increased to 100% after 10 min reduction at 450 °C, but upon heating in hydrogen for an additional 10 min at 500 °C it decreased again to 75%. In another series of experiments the mixed oxide was reoxidized after each reduction. A fresh sample was reduced to 350 and 400 °C by contacting with hydrogen for 1 hr and evacuated at temperatures between 400 and 500 °C. Both high evacuation temperatures and reduction at 400 °C during 1 hr produced a sharp decrease in Co° surface concentration. These results are consistent with the catalytic behavior of this perovskite reported earlier by E. A. Lombardo et al. (4–7). A model is proposed to interpret the reduction of LaCoO3. 相似文献
6.
Isamu Yamauchi Takashi Okamoto Hajime Ohata Itsuo Ohnaka 《Journal of Alloys and Compounds》1997,260(1-2):162-171
The effects of Cu addition on the β phase formation rate and the thermoelectric power in various FeSi2 and Fe2Si5 based alloys was examined. The peritectoid reaction (a+→β) in FeSi2 alloys was initially enhanced by the addition of Cu but it became slower for longer annealing times. The retained metallic ε was harmful for the thermoelectric power. The inherent thermoelectric properties of (FeSi2)99−XMn1CuX (X=0–1.O at.%), (FeSi2)99−X Co1CuX (X=0–1.0 at.%) alloys were attained after the elimination of ε. In the case of eutectoid reaction (→β+Si). Differential thermal analysis, X-ray diffraction and microscopic observation clearly confirmed that the eutectoid reaction rate was drastically enhanced by the addition of a small amount of Cu and its rate decreased with decreasing Cu content. The rate also depends on the annealing temperature and reached a maximum at about 1073 K for most alloys. The addition of only 0.1 at.% Cu was still very effective even in Mn or Co doped alloys. The thermoelectric power of these alloys increased very quickly with annealing time. Their final values decreased with Cu content and saturated at 0.2 at.% Cu. The value of the 0.1 at.% Cu added alloy was higher than that of both the conventional p- and a-type FeSi2 based alloys. These results suggest that the Fe2Si5 alloys with a small amount of Cu may be attractive as new thermoelectric materials. 相似文献
7.
Crystallite size distribution and the lattice distortions in highly γ-irradiated linear polyethylene
Crystallite size distributions and lattice distortions have been analysed for highly-irradiated linear polyethylene in the direction normal to 1 1 0 and 0 0 1 lattice planes through X-ray line profile analysis. It has been found that the lateral crystallite size is little affected irradiation greater than 1000 Mrad, whereas that in the chain direction decreases almost linearly with the dose of irradiation. A minor difference in the crystallite size between irradiation atmospheres, i.e. irradiation in air or in vacuum, has been disclosed at a very high dose of irradiation. The above degradation behaviour of crystallites and the change in lattice distortions have proved that radiation cross-links are mainly formed in the amorphous region near the lamellar surface of polyethylene. 相似文献
8.
Gang Yang Junchu Li Gaochao Wang Masatomo Yashima Silin Min 《Journal of Materials Science》2005,40(23):6087-6090
Influences of ZrO2 nanoparticles on the mechanical properties and microstructure of hot-pressing Ce-TZP/Al2O3 ceramics were investigated. Meanwhile, t-ZrO2 to m-ZrO2 transformation toughening mechanism was investigated by X-ray diffractometry (XRD) method, and deflection of samples under
applied stress were recorded too. The results show that when the percentage of ZrO2 was 20%, the mechanical properties and microstructures of materials are optimum. Moreover, TEM observation show dislocation
structures formation both in the Al2O3 and on the grain boundary. Because the dislocation agglomeration and fixation by ZrO2 nanoparticles could deflect cracking or stop cracking development, a strengthening and toughening effect could be achieved. 相似文献
9.
10.
Isamu Ogura Mari Kotake Hiromu Sakurai Kazumasa Honda 《Aerosol science and technology》2016,50(8):846-856
The flat surface of Nuclepore filters is suitable for observing collected particles with a scanning electron microscope (SEM). However, experimental data on surface-collection efficiency are limited because surface-collection efficiencies cannot be measured directly using aerosol measuring instruments. In this study, the surface-collection efficiencies of Nuclepore filters were determined by establishing the ratio of the number of particles deposited on the surface of the filter visually counted with an SEM to the number of inflow particles counted by a condensation particle counter, using monodispersed polystyrene latex particles (30–800 nm) and silver particles (15–30 nm). Because Nuclepore filters with smaller pore sizes would be expected to produce higher minimum surface-collection efficiency and a higher pressure-drop, 0.08 and 0.2 µm Nuclepore filters were chosen as the test filters in view of both collection efficiency and pressure drop. The results showed that the minimum surface-collection efficiencies of the 0.08 µm pores at face velocities of 1.9 and 8.4 cm·s?1 were approximately 0.6 and 0.7, respectively, and those of the 0.2 µm pores at face velocities of 1.5 and 8.6 cm·s?1 were approximately 0.8 and 0.6, respectively. Because the pressure drop of the 0.2 µm pore filter was lower than that of the 0.08 µm pore filter under the same flow-rate conditions, the 0.2 µm pore filter would be more suitable considering the pressure drop and collection efficiency. The obtained surface collection efficiencies were quantitatively inconsistent with theoretical surface-collection efficiencies calculated using conventional theoretical models developed to determine the collection efficiency of filters with larger pores.© 2016 American Association for Aerosol Research 相似文献