三次样条构造的伪逆解法

为了提高三次样条构造的可行性, 基于矩阵的伪逆方法, 提出一种不依赖额外约束条件的三次样条构造的伪逆解法。该解法通过求解出三次样条二阶导数的最小范数解, 从而较好地构造出三次样条函数。理论分析及数值实验结果表明该三次样条构造的伪逆解法具有简单、有效等特点。综合分析各种构造解法的性质, 对各种三次样条构造解法进行归类比较, 为在实际工程计算应用中选择合适的三次样条构造解法提供了指导方向。     

纳米CaSiO_3填料的制备及其性能表征

以乙醇为溶剂,正硅酸乙酯(TEOS)为胶溶剂,CaCO3为主要试剂,采用溶胶-凝胶(Sol-Gel)技术制备纳米偏硅酸钙(CaSiO3)填料,考察主要工艺参数——初始水凝胶pH值、R值(H2O/TEOS)对粉体形貌、颗粒大小等性质的影响。研究表明:采用溶胶-凝胶法能合成纳米级的CaSiO3填料。     

陶瓷材料在微机电系统中的应用

在微机电系统(MEMS)中应用到了许多种材料,其中,使用最多的是陶瓷材料。本文分析了当前国内外在MEMS研究中 的陶瓷材料的应用现状。着重分析了在MEMS中硅作为结构材料的应用以及作为薄膜材料的应用,此外,还介绍了其它 一些在MEMS中常见的陶瓷材料,如碳化硅、氮化硅、PZT压电陶瓷等材料的性能和应用。     

The effect of radical desorption on the particle size distribution in vinyl acetate emulsion polymerization

The effect of free radical desorption is studied by using a mathematical model of particle size distribution in continuous emulsion polymerization. By comparing the theoretical prediction with experimental data, the value of D_o for the vinyl acetate (VAc) system is best chosen as 0.19 × 10^?7 cm²/h. The effect of radical desorption as well as mean residence time on the absolute particle size distribution, total concentration of polymer particles, conversion, and average number of radicals per polymer particle are analyzed by the model proposed.     

Hydrothermal Synthesis of CdMoO4 Nano-Particles

CdMoO₄ nano-particles were successfully synthesized by a hydrothermal process at a low temperature of 90°C, and the powders were characterized in detail by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and photoluminescent spectra techniques (PL), respectively. CdMoO₄ particles could be obtained under the hydrothermal condition from micrometer to nanometer sizes by varying their precursors. The PL spectra results showed that the optical properties of CdMoO₄ crystallites obviously relied on their particle sizes.     

稀土基汽车尾气催化剂的研究Ⅰ:催化剂老化和SO_2添加对催化活性的影响

制备了低Pt、Rh担载量的稀土基催化剂体系 ,研究了贵金属担载量、催化剂高温老化、抗硫水热老化和SO2 对催化活性的影响。结果表明 :随着贵金属质量分数从 0 2 5 %降低到0 1% ,CO、碳氢化合物 (HC)和NO的起燃温度分别平均提高 2 0℃ ;随着m(Pt)∶m(Rh)从 5∶1提高到 9∶1,CO、HC和NO的起燃温度分别提高 17、2 0和 5 3℃ ;当在反应体系中添加SO2 ,随SO2 体积分数从 0 0 0 2 %增加到 0 0 1% ,CO和NO的起燃温度和完全转化温度分别平均提高2 0℃ ,而对于HC ,催化活性几乎保持不变 ;催化剂在水热含硫条件下连续老化 4 0 0h ,CO、NO和HC的起燃温度分别为 2 5 2、2 6 7和 30 3℃ ,仍具有良好的反应活性。表明该稀土基催化剂在一定条件下 ,能满足汽车实际工况的要求     

一种无人机生成平滑航迹方法的研究与实现

无人机在未来战场中占有重要地位,航迹规划直接影响其作战能力。针对无人机航迹规划算法中存在的问题,提出一种生成平滑航迹的方法。该方法解决了直角拐弯、航迹不平滑、规划航迹与实际航迹不一致的问题。最后,通过VC++6.0+mapX5.0编程实现,结果表明了该方法的优势。     

聚(L-谷氨酸-γ-苯甲酯)接枝共聚物的合成

以溶液聚合直接合成聚丙烯酸,通过接枝反应将疏水的聚肽链接到聚丙烯酸亲水链段上形成两亲性共聚物,合成了新型聚肽接枝共聚物。用核磁共振等方法表征了接枝共聚物的存在。实验结果表明其在含有钠离子的水溶液中能自行组装成为高聚物纳米胶束。     

Gel formation in diimide‐hydrogenated polymers

The hydrogenation of diene‐based polymers via diimide is a very attractive alternative to the conventional catalytic hydrogenation route based on gaseous molecular hydrogen. However, serious crosslinking always accompanies it and limits the end‐use properties of the polymers. Gel formation in polymers that are hydrogenated via diimide has been investigated in detail through an inspection of all the chemical reactions involved in the process. The results indicate that hydrogen peroxide decomposition, some reactions related to oxygen, and the redox reaction between hydrogen peroxide and hydrazine are capable of generating radicals. However, radicals generated in the aqueous phase do not appear to initiate the crosslinking of diene‐based polymers in the latex form. It is proposed that the primary radicals giving rise to crosslinking are generated in the polymer phase in situ, and the step responsible for generating these organic radicals is possibly the diimide disproportionation reaction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1122–1125, 2005     

The morphology and conductivity of polypyrrole/polyurethane alloy films

Polymeric composites with conductivities ranging from 10^–4 to 1 S cm^–1 were prepared by electrochemically polymerizing pyrrole in a matrix of polyurethane. The polypyrrole/polyurethane alloy films obtained were characterized by element analysis, electron microscopy and electrical conductivity measurements. The morphology of the films depended on the solvent, the electrolyte and the current density. The mechanism of the electrochemical polymerization showed that PPy grew in a treelike structure, with molecular chains extending from the electrode surface into the solution. The transition temperature of the PPy/PU increased with the PPy content.