超声参振对Al-Fe合金凝固过程的影响

在Al-Fe合金的凝固过程中引入不同功率的超声振动,利用受控凝固和受控振动相结合的实验装置和方法,研究了超声参振对Al-Fe合金熔体温度场以及组织形态和抗拉强度的影响.实验表明:熔体的温度场随振动功率的增加和振动时间的延长而升高,并趋于一个平衡的温度场;超声参振可以显著细化先共晶FeAl3相,Al-Fe合金生长的组织形态的差异主要取决于凝固速度;超声参振凝固的Al-Fe合金的热稳定性好,有良好的应用前景.     

热压变形对灰口铸铁石墨形态的影响

研究了灰口铸铁(HTl50)在900℃大压下量塑性变形后石墨的分布形态，结果表明：随着压下量的增加，石墨片逐渐趋于平行分布；变形过程中发生了碳的回溶，同时伴随着石墨片的断裂；石墨片体积分数及片间距随压下量的增加而逐渐减少。     

添加剂硫对Ni-Mn-Co粉末触媒合成金刚石的影响

本研究考察了高温高压条件下添加剂硫对Ni-Mn-Co粉末触媒合成金刚石的影响，并在此基础上，考察了含硫金刚石的机械性能。研究表明：硫对Ni70Mn25Co5粉末触媒合成金刚石的成核有明显的抑制作用，随着硫含量的增加，成核呈减少趋势；添加剂硫影响晶体的颜色和晶形，随添加剂含量的增加，晶体的颜色呈加深趋势，硫的添加使晶体的表面出现孔洞缺陷，当硫含量较低时，孔洞缺陷多分布在（100）晶面上，当硫含量较高时，（111）晶面上也出现孔洞，致使晶体的完整性受到制约；添加剂硫影响金刚石的机械性能，随着添加剂硫含量的增加，含硫金刚石的冷冲击强度（TI）和热冲击强度（TTI）呈明显的下降趋势。     

含Li的Al-Zn-Mg-Cu合金沉淀析出过程的定量分析

应用小角度X射线散射技术结合TEM分析定量的描述Al-Zn-Mg-Cu-Li合金时效过程中析出相尺寸分布和形貌等信息。通过分析确定合金在几种时效状态下析出相为轴比在0．2～0．4之间的扁回转椭球形。确定了析出相特征尺寸的对数正态分布和质量依回转半径的Maxwell分布。并分析分布曲线随动力强度Ks的变化特征，可以看出，析出相尺寸和质量分布曲线基本满足随动力强度增加，几何平均值增加，分布范围变宽。     

熔体过热处理对定向凝固界面形态及稳定性的影响

介绍了固液界面形态及稳定性的判据,即成分过冷理论和绝对稳定理论;简述了国内熔体过热处理的研究;详细阐述了熔体过热处理影响定向凝固界面形态及稳定性的现象及理论研究.并对今后熔体过热处理在定向凝固技术中的研究方向作了展望.     

形态对钯-氢体系热力学性质的影响

基于实验测定海绵Pd颗粒在278K-323K范围内吸放H2，D2的P-C-T曲线．结合文献给出的其它形态的Pd吸放氢结果进行系统比较分析．探讨了形态对钯-氢体系热力学性质的宏观影响和微观本质。在室温附近，氢的饱和固溶度与坪压随Pd的粒度减小而增加；Pd的形态或粒度对氢的饱和固溶度和吸氧坪压的影响程度刚随温度升高而减小，而且坪压之间的差别在温度较高时不再明显甚至消失。吸氘坪压差别大，解吸坪压差别小。Pd—H体系中α→β的相变热焓、热熵（绝计值)随粒度减小而减小，单晶Pd相应热力学函数最小。海绵Pd颗粒中的压力迟滞效应最明显．材料本底缺陷密度决定不同形态Pd-H体系的压力迟滞效应的大小。     

PP／mPE／无机填料三元复合材料的形态结构和力学性能

采用刚性无机填料对茂金属聚乙烯（mPE)弹性体增韧聚丙烯（PP）二元共混体系进行增强，从而制得PP／mPE无机填料三元复合材料。分别探讨了CaCO3用量对复合材料拉伸性能和低温冲击性能影响，并考察了不同填料的增强效果。实验结果表明，由于弹性体的存在，无机填料的增强作用减弱；共混物的低温冲击强度也因填料的加入而大幅度下降，但经过表面处理的高岭土体系的冲击强度反而提高。SEM断裂形貌显示，未经表面处理的填料和基体的界面结合较弱，而改性高岭土则以层状结构分散于基体中，并呈现牢固的界面结合。     

Polylactide films formed by immersion precipitation: Effects of additives,nonsolvent, and temperature

The influence of nonsolvent, crystallinity of the polymer film, and addition of dodecane (a poor solvent for the polymer and for the nonsolvent) on the morphology of polylactides films has been investigated and was related to phase separation behavior. Both amorphous poly‐DL ‐lactide (PDLLA) and crystalline poly‐L ‐lactide (PLLA) were dissolved in dichloromethane, and subsequently films were made by immersion in nonsolvent baths. PDLLA gave dense films without any internal structure, since the structure was not solidified by crystallization or glassification. PLLA films show varying structure depending on the nonsolvent. With methanol, asymmetric morphologies were observed as a result from combined liquid‐liquid demixing and crystallization, while with water symmetric spherulitic structures were formed. As a next step, dodecane was added, which is not miscible with the nonsolvent, and we found it to have a strong influence on the morphology of the films. The PDLLA films with dodecane did not collapse: a closed cell structure was obtained. In PLLA films, dodecane speeds up phase separation and induces faster crystallization in the films, and the porosity, size of the pores, and interconnectivity increased. When the PLLA solutions were subjected to a heat pretreatment, crystallization could be postponed, which yielded a cellular structure around dodecane, which did not contain spherulites anymore. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 959–971, 2007     

Initial stages of tin electrodeposition from sulfate baths in the presence of gluconate

Tin electrodeposition in its initial stages in acid sulfate/gluconate baths was studied with varying tin and gluconate concentrations using potential-controlled electrochemical techniques. The deposit morphology was observed by scanning electron microscopy (SEM). A comparison with tin electrodeposition from acid sulfate baths in the absence of gluconate was also carried out. Use of a highly acidic bath leads to nonuniform deposits, even in the presence of gluconate; at pH 4 deposits are uniform, brilliant and suitable for finishing applications. Tin crystallites have a well defined morphology which depends on bath agitation conditions. In the absence of agitation, the crystallites have the same tetragonal shape as in a sulfate bath without gluconate.     

Properties of poly(n‐butyl methacrylate) prepared by reverse atom transfer radical polymerization in an aqueous dispersed system

Reverse atom transfer radical polymerization (ATRP) of n‐butyl methacrylate (BMA) in waterborne media using Cu(II) complexes with azo initiators (i.e., reverse ATRP) was conducted. The influence of several factors, such as surfactant, catalyst, and reaction time, on the stability of the emulsion, the particle size, the morphology of the emulsion particles, and the control of the polymerization was investigated. The results showed great differences between ATRP and conventional emulsion polymerization, especially the nucleation mechanism and the kinetics. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1542–1547, 2003