纳米W-Cu粉末的均相沉淀法制备及其烧结性能

采用湿化学工艺--蒸氨均相沉淀法,制备了纳米CuWO4·2H2O/Cu2WO4(OH)2均相沉淀物,然后煅烧、还原,得到含Cu 30%的W-Cu复合粉.将该复合粉压坯在H2气氛中于不同温度下烧结后,对烧结体的微结构和物理、力学性能等进行了测试分析.实验结果表明:蒸氨均相沉淀法制备的W-Cu复合粉体具有纳米粒度和均匀的化学组成,其烧结活性高,在较低温度下烧结即可达很高的致密化程度.由上述W-Cu粉体所制备的烧结体具有良好的物理、力学性能.     

Development of microstructure and mechanical properties of a Ni-base single-crystal superalloy by hot-isostatic pressing

Effects of the hot-isostatic pressing (HIP) process on microstructures and mechanical properties of Ni-base single crystal superalloy CMSX-4 were investigated. In the overall heat treatment process, the HIP treatment remarkably induced the healing behavior of micropores and decreased the pore size and porosity of superalloy CMSX-4 compared with normally treated specimens. The microstructure of γ′ phase after the HIP process showed rather a coarsening tendency and could be developed by the partially solution and aging treatment. Consequently, the elimination of cast micropores using the HIP step resulted in the inhibition of crack initiation in microstructure and improved the stress-rupture lives of Ni-base single crystal superalloy by 185%.     

粉末冶金法制备SiC晶须增强MB15镁基复合材料

采用粉末冶金法制备了SiC晶须增强镁基复合材料(SiCW／MB15)试样。通过检测基体显微硬度探讨了SiCW对镁合金时效规律的影响，并借助扫描电镜(SEM)、透射电镜(TEM)和拉伸试验，研究了混粉方式对复合材料室温力学性能、SiCW分布及显微结构的影响。结果表明，MB15及其复合材料的时效硬化曲线上均存在双峰现象；SiCW的加入既提高了MB5的硬度，又加快了其时效速度：混粉方式对晶须分布及SiCW／MB15复合材料的室温力学性能影响很大。     

注射成型塑化过程的可视化实验研究

利用自行开发的可视化实验装置对注射成型的塑化过程进行了系统的观察,着重讨论了不同的工艺条件对塑化性能的影响,同时借助示踪粒子对塑化过程的重要参数——固相速度进行了测量。实验所取得的数据为注射成型熔融模型的建立和对模型的验证提供了依据,同时也是注射螺杆优化设计的基础数据。     

环形截面提升管内颗粒的运动行为

采用PDPA(phase Doppler particle analyzer system)及磷光颗粒示踪技术对环形截面提升管中颗粒的运动行为进行了研究。与传统提升管相比，环形截面提升管中颗粒速度分布的均匀性有所改善，其最高速度与最低速度之差变小。环形截面提升管最大速度值出现在相对径向位置φ=0.3-0．4处。与传统提升管相似，环形截面提升管内颗粒的轴向返混较严重，停留时间分布曲线存在较明显的拖尾，其中颗粒的轴向Peclet数与传统提升管也处于同一数量级范围。提升管床结构的改变并未显著改变其中气固流动的微观相结构，稀相与密相颗粒团微观两相仍然存在，这种微观相结构是造成颗粒严重返混的决定性原因：稀相中的颗粒与密相颗粒团中的颗粒分别造成了颗粒停留时间分布曲线的前峰与拖尾峰。     

酚醛树脂注塑料的化学流变行为研究

利用Brabender流变仪，考察了酚醛树脂注塑料的化学流变特性，根据双阿累尼乌斯方程建立了酚醛树脂注塑料的化学流变模型。该模型与实验结果具有较好的一致性，利用该模型可以预测酚醛注塑料注塑所需要的工艺窗口，并能动态模拟整个注塑过程中的黏度变化。     

Thermal analysis of polymer–water interactions and their relation to gas hydrate inhibition

Gas hydrates formed in oil production pipelines are crystalline solids where hydrocarbon gas molecules such as methane, propane, and their mixtures are trapped in a cagelike structure by hydrogen‐bonded water molecules to form undesirable plugs. Methanol and glycol are currently used to prevent these plugs via thermodynamic inhibition. Small amounts of water‐soluble polymers may provide an alternate approach for preventing gas hydrates. In this study, we expand the fundamental understanding of water–polymer systems with differential scanning calorimetry. Nonfreezable bound water was used to quantify polymer–water interactions and relate them to the chemical structure for a series of polymers, including acrylamides, cyclic lactams, and n‐vinyl amides. For good interactions, the water structure needs to be stabilized through hydrophobic interactions. An increased hydrophobicity of the pendant group also appears to favor polymer performance as a gas hydrate inhibitor. Good inhibitors, such as poly(diethyl acrylamide) and poly(N‐vinyl caprolactam), also show higher heat capacities, which indicate higher hydrophobicity, than poor performers such as polyzwitterions, in which hydrophilicity dominated. The phase behavior and thermodynamic properties of dilute polymer solutions were also evaluated through measurements of the heat of demixing and lower critical solution temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2642–2653, 2007     

Tasting green leaf volatiles by larvae and adults of Colorado potato beetle,Leptinotarsa decemlineata

Larvae and adults of the Colorado potato beetle,Leptinotarsa decemlineata (Say), are shown to have galeal gustatory cells that are highly sensitive to distillate of potato leaf extracts, (E)-2-hexen-1-ol, (E)-2-hexenal, and other saturated and unsaturated six-carbon alcohols. In larvae and adults, the sensory response patterns elicited by leaf homogenate, leaf distillate and a mixture of these two extracts differ in subtle ways. Beetle larvae feed most readily on Millipore disks treated with leaf homogenate and the mixture, but they did not feed on disks treated with leaf distillate. The differences in behavioral response and sensory input are used to derive a potential gustatory code that may stimulate different levels of feeding. This code may be disrupted by compounds present in nonhost leaves, thus leading to reduced feeding. Possible interactions of sapid leaf volatiles, amino acids, sugars, and potentially deterrent plant compounds are discussed.     

锂电极表面膜的组成和阻抗行为

介绍了锂电池中锂电极的表面膜的组成和阻抗行为，并根据其表面膜的阻抗行为提出了电化学模型。     

Effects of substituted aromatic heterocyclic phosphate salts on properties,crystallization, and melting behaviors of isotactic polypropylene

Nucleation effects of 2,2′‐methylene‐bis (4,6‐di‐tert‐butylphenyl) phosphate metal salts as a nucleating agent for isotactic polypropylene (iPP) were investigated with differential scanning calorimeter and polarized optical microscope, and their effects on mechanical, optical, and heat resistance properties of iPP were also studied. The results showed that monovalent metal salts of substituted aromatic heterocyclic phosphate such as sodium salt, lithium salt, and potassium salt had a good performance. With 0.2 wt % of sodium salt, lithium salt, or potassium salt incorporated into iPP, the crystallization peak temperature of iPP could be increased by 13.5, 13.6, and 15.0°C, respectively; the mass fraction of crystallinity of iPP could be increased by about 5%; and crystallization rate was enhanced increasingly. Meanwhile the tensile strength and flexural modulus of iPP could be increased by about 10 and 30%, respectively, and the clarity and heat distortion temperature of iPP could also be improved significantly. But bivalent and trivalent metal salts of substituted aromatic heterocyclic phosphate had little effect on properties of iPP. Meanwhile the morphology study showed that the addition of monovalent sodium salt could decrease the spherulite size of iPP significantly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4868–4874, 2006