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But the question is: AlN / BN composite ceramic sintering very difficult.

但目前存在的问题是:AlN/BN复相陶瓷的烧结非常困难。

A reparing material for reparing the coke oven by spraying the semi-dried it is prepared from the raw Al-Si material chosen from mullite, high-Al alumine, etc.

焦炉修补用半干法喷补料,其组分及组分重量百分比为:铝硅质原料55~78%、结合剂10~25%、烧结剂和可塑剂3~5%、膨胀剂3~7%、Al 2 O 3 微粉或/和SiO 2 微粉5~10%;外加剂加入量为总量的0.1~1.0%。

Aluminothermic reactive synthesis of Al2O3-TiC nanocomposite powders from a mixture of TiO2, Al, and C powders induced by high-energy ball milling and its consolidation through spark plasma sintering were investigated.

以TiO2、Al、C为原料,首先采用高能球磨引导铝热反应合成了Al2O3-TiC 纳米复合粉体,然后采用放电等离子体烧结纳米复合粉体制备了Al2O3-TiC复合材料。

The structure measurement indicates that only a small amount of Bi3+ ions can not enter the A-site of La2/3Ca1/3MnO3 lattice. Because of the low melting behavior of bismuth oxide, the superfluous Bi will segregate as insulating bismuth oxides and bismuthate. Because of the segregation of Bi, the surface of the main phase has different ferromagnetic property from that of the core, namely the magnetic inhomogeneity of the samples is enhanced, which results in the broader ferromagnetism-paramagnetism transition and magnetoresistance plateaus in samples with the high Bi content.

结构测试表明Bi并不能进入La2/3Ca1/3MnO3的晶格锰位,由于A位元素的过量和铋氧化物的低熔点特性,烧结过程中Bi元素析出形成了绝缘性的第二相;并且Bi的析出导致样品主相的表面存在与主相体心磁性质不同的铁磁相,即样品的磁不均匀性增强,使得高Bi含量的样品表现出宽的铁磁-顺磁转变和磁电阻平台效应。

Sinter type straight-handle drills:Use for drilling hard and brickle marerial,...

烧结直柄钻头:适用于玻璃、陶瓷、宝石等硬脆材料的钻孔。

Sinter type straight-handle drills:Use for drilling hard and brickle marerial,such...

摘 要:烧结直柄钻头:适用于玻璃、陶瓷、宝石等硬脆材料的钻孔。

The structural and photocatalytic properties of TiO〓 as well as surface acidity were greatly improved by sulfation. SO〓〓/TiO〓 solid superacid with Hammett constant Ho less than -12.14 was prepared by treating the TiO〓 with 1.0mol. L〓 sulfuric acid solution and then calcining at 450℃ for 3h. When compared to unmodified TiO〓, the SO〓〓/TiO〓 superacid catalyst exhibited higher anatase content, smaller crystal size, higher specific surface area, centralized pore size distribution, and the blue-shifted band edge of uv-vis adsorption spectra. Furthermore, the SO〓〓/TiO〓 superacid also showed excellent reaction activity and stability for CH〓Br photocatalytic decomposition even under the moist reaction conditions. The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明:SO〓〓与TiO〓表面的结合为螯合式双配位结构;TiO〓光催化剂表面经H〓SO〓浸渍处理后,提高了表面酸性,改善了催化剂结构和光催化性能,当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时,可制得SO〓〓/TiO〓超强酸催化剂(H〓<-12.14),其结构和光催化活性得到明显改善,与TiO〓相比,SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移,具有优异的光催化氧化活性、稳定性及抗湿性能,光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级,是一种有实际应用前景的高效光催化剂;由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型,认为在SO〓〓/TiO〓超强酸催化剂表面,由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心,其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移,具有可逆吸附水的性能,是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明:SO〓〓与TiO〓表面的结合为螯合式双配位结构;TiO〓光催化剂表面经H〓SO〓浸渍处理后,提高了表面酸性,改善了催化剂结构和光催化性能,当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时,可制得SO〓〓/TiO〓超强酸催化剂(H〓<-12.14),其结构和光催化活性得到明显改善,与TiO〓相比,SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移,具有优异的光催化氧化活性、稳定性及抗湿性能,光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级,是一种有实际应用前景的高效光催化剂;由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型,认为在SO〓〓/TiO〓超强酸催化剂表面,由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心,其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移,具有可逆吸附水的性能,是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The microstructure and phase composition of needle shaped,calcium-deficient hydroxyapatite coating, with or without brushite,on Ti6Al4V substrate prepared by electrochemical deposition -hydrothermal treatment,subsequently sintered at 450—980℃ in air atmosphere were studied.

研究了Ti6Al4V表面针状缺钙羟基磷灰石涂层在450—980℃空气中烧结后的相组成和显微结构及磷酸氢钙相的影响,分析了缺钙羟基磷灰石的高温分解行为。

To find and confirm the most effective preparing technology, the effect of sintering temperature and calefactive velocity upon mechanical properties and microstructures of the materials before and after infiltration were studied. In order to control the coefficient of thermal expansion and colors of the glass as well as the fluidity and infiltration property of the melted glass, we modified the formula of the glass.

在材料制备的同时,研究和比较了氧化铝升温速率及烧结温度对玻璃渗透前后材料的力学性能和微观结构的影响,以期寻求最佳的制备工艺;并改进渗透玻璃配方,以调控玻璃的热膨胀系数和颜色以及在高温下的流动性、浸润性。

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呼气,收缩臀部肌肉;拱起身体,尽量抬起头来,右腿伸直朝向天花板(膝微屈,以避免肌肉紧张)。

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