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排序方式: 共有266条查询结果,搜索用时 15 毫秒
1.
Si3N4 ceramic was jointed to itself using a filler alloy of Cu76.5Pd8.5Ti15, and the mechanical properties of the jointwere measured and analyzed. By using a filler alloy of Cu76.5Pd8.5Ti15, the SisN4/SisN4 joints were obtained bybrazing at 1373~1473 K f 相似文献
2.
Group-velocity dispersion (GVD) compensation in in-line amplifier systems is evaluated from the viewpoint of improving the transmission distance. The nonlinear Schrodinger equation, which simulates signal propagation in optical fibers, is numerically evaluated to clarify the optimum configuration for GVD compensation. It is shown that the optimum amount of GVD compensation is about 100% of the GVD experienced by the transmitted signal. The optimum compensation interval is found to be a function of the bit rate, signal power, and dispersion parameter. For dispersion parameter values ranging from about -0.1 ps/nm/km to -10 ps/nm/km, and an amplifier noise figure of about 6 dB, the optimum compensation configuration can eliminate the GVD from in-line amplifier systems, thus improving transmission distances to those limited by self-phase modulation and higher-order GVD 相似文献
3.
Numerical analysis of IM signal propagation in an optical fibre is carried out taking selfphase modulation and group-velocity dispersion into account. The transmission distance yielding a prescribed eye opening penalty, in the normal dispersion region, is shown to be inversely proportional to the square root of the signal power.<> 相似文献
4.
Hydrothermal synthesis and in situ surface modification of boehmite nanoparticles in supercritical water 总被引:2,自引:1,他引:1
T. Mousavand S. Ohara M. Umetsu J. Zhang S. Takami T. Naka T. Adschiri 《The Journal of Supercritical Fluids》2007,40(3):397-401
In situ surface modification of boehmite (AlOOH) nanoparticles during hydrothermal synthesis in supercritical water was examined by adding CH3(CH2)4CHO and CH3(CH2)5NH2 as modifier reagents to the reactants. Changes in surface properties of the nanoparticles by surface modification was observed by FTIR, dispersion in solvents and TEM analyses, which demonstrated that reagents chemically binded onto the surface of the AlOOH nanoparticles. The results of SEM and TEM pictures show that the surface modification affects crystal growth and reduces the particle size and changes the morphology of the particles. 相似文献
5.
Boron nitride (BN) of low crystallinity was synthesized from triammoniadecaborane (TAD) and hydrazine at 125 MPa below 650° C. TAD itself was pyrolysed at 600° C and 125 MPa to form a mixture of amorphous boron and boron nitride containing BH and NH bonds. The infrared spectrum of the pyrolysed product of TAD itself at 600° C and 125 MPa showed the BNB absorption at 800cm–1 due to the formation of B3N3 structures. The X-ray diffraction (XRD) of the reaction product from TAD and hydrazine at 600° C had broad diffractions centred at 2=25.5° and 43.0° (CuK). The BH absorption at 2500cm–1 decreased in intensity on increasing the N/B ratio from 0.3 to 0.85, and disappeared finally at a ratio of N/B=1.3. The reaction product at 125 MPa had a porous structure. The electron diffraction of the specimen changed from faint rings to spots on circular rings after heat treatment at 800° C for 10 h. The heat-treated specimen, however, did not give sharp reflections corresponding to hexagonal BN in the XRD profile. BN of low crystallinity was transferred to cubic BN at 1200° C and 6.5 GPa in a 90% yield, which was higher than that of well-crystallized BN in the presence of AIN. 相似文献
6.
Hideaki Itoh Shigeharu Naka Tsuneaki Matsudaira Hiroshi Hamamoto 《Journal of Materials Science》1990,25(1):533-536
A sintered compact of titanium diboride (TiB2) was prepared by hot pressing of the synthesized TiB2 powder, which was obtained by a solid-state reaction between TiN and amorphous boron. Densification of the sintered compact occurred at 20 MPa and 1800° C for 5 to 60 min with the aid of a reaction sintering, including the TiB2 formation reaction between excess 20 at % amorphous boron in the as-synthesized powder (TiB2 + 0.2B) and intentionally added 10 at % titanium metal. A homogeneous sintered compact of a single phase of TiB2, which was prepared by hot pressing for 30 min from the starting powder composition [(TiB2 + 0.2B) + 0.1 Ti], had a fine-grained microstructure composed of TiB2 grains with diameters of 2 to 3 m. The bulk density was 4.47 g cm–3, i.e. 98% of the theoretical density. The microhardness, transverse rupture strength and fracture toughness of the TiB2 sintered compact were 2850 kg mm–2, 48 kg mm–2 and 2.4 MN m–3/2, respectively. The thermal expansion coefficient increased with increasing temperature up to 400° C and had a constant value of 8.8 x 10–6 deg–1 above 500° C. 相似文献
7.
Hideaki Itoh Tsuneaki Matsudaira Shigeharu Naka Hiroshi Hamamoto 《Journal of Materials Science》1989,24(2):420-424
TiB2 powder was synthesized by a controlled formation reaction from titanium metal and amorphous boron. Precursory TiB2 formed by the pretreatment of the mixed powder (mole ratio: B/Ti=2.0) at 600° C for 60 min in an argon stream. Hollow TiB2 powder with an average grain size of 15m was obtained by subsequent heat treatment above 900° C for more than 60 min in an argon stream. The formation reaction of TiB2 powder was further controlled by pretreatment of the mixed powder at 600° C for 60 min in a hydrogen and argon stream and subsequent heat treatment at 1000° C for 360 min in an argon stream, when hollow-free TiB2 powder was formed by a milder formation reaction between amorphous boron and the reformed titanium metal with hydrogen diffused lattice. 相似文献
8.
Shin-ichi Hirano Akira Fujii Toshinobu Yogo Shigeharu Naka 《Journal of the American Ceramic Society》1990,73(8):2238-2241
Cubic BN was synthesized under high-temperature and -pressure conditions from BN powder formed by pressure pyrolysis of borazine below 700°C and 100 MPa. The conversion of BN powder to cubic BN was strongly influenced by the residual hydrogen identified by the BH/BN ratio of IR absorption band. The activation energy for cubic BN synthesis from BN powder-20 mol% AIN was 46 kJ/mol, when the starting BN was synthesized at 250°C. A mixture of BN powder and cubic BN particles was converted to cubic BN in a 100% yield by heat treatment at 1800°C and 6.5 GPa without any catalyst. The presence of cubic BN particles does enhance the conversion to cubic BN from BN powder. The energy required for the transformation of starting BN to cubic BN in the presence of cubic BN seed was 355 kJ/mol. 相似文献
9.
Nanocrystalline Ni3Al was fabricated through mechanical alloying of elemental powders and spark plasma sintering. The nanocrystalline Ni3Al has a nearly full density after being sintered at 1223 K for 10 min under a pressure of 65 MPa. Isothermal and cyclic oxidations of nanocrystalline Ni3Al were tested at 1173–1373 K with intervals of 100 K. The results indicate that nanocrystalline Ni3Al exhibits excellent isothermal and cyclical oxidation resistance. The oxide scales consist primarily of dense and continuous -Al2O3. The grain refinement is beneficial for improving the oxidation resistance of Ni3Al by providing more nucleation centers for the Al2O3 formation, promoting the selective formation of Al2O3 and improving the adhesion of oxide scales to the matrix. 相似文献
10.
Kenichi Mori Michiaki Sakamoto Jin Matsushima Daisuke Inoue Kenichirou Naka Ken Sumiyoshi 《Journal of the Society for Information Display》2009,17(6):513-518
Abstract— In order to improve the reflective contrast ratio of transflective IPS‐LCDs, a novel pixel design for a normally white reflective IPS has been proposed. In this design, the large‐inter‐electrode‐spacing layout using a novel driving method and a double‐layered electrode have effectively reduced the light leakage. By applying these two technologies, a transflective IPS‐LCD has been successfully demonstrated with a high contrast ratio (15:1) in the reflective mode and a wide‐viewing‐angle characteristic in the transmissive mode. 相似文献