U-5．7Nb合金的微观变形机制

一般认为，处于单斜α”相的U-5．7Nb合金室温下的塑性变形主要是孪晶界面的移动，而不是由于滑移位错的移动，但这些都是居于理论上的推测，没有具体的实验证据。因此利用现有的电子显微分析技术，原位观察研究U-5．7Nb合金在变形过程中的微观机制，从而揭示微观结构与宏观性能之间的联系十分必要。在透射电镜（TEM）中进行原位拉伸观察裂纹的形核和扩展是有效的方法。利用H-800透射电镜的原位拉伸实验台对U-5．7Nb合金进行原位微观断裂研究。     

添加Ti对Al-Bi难混溶合金组织和性能的影响

难混溶合金在凝固过程中极易发生液-液相分离,造成第二相的宏观偏析,失去了合金的应用价值.本文将第三组元Ti添加到Al-Bi难混溶合金中,研究了Ti的添加对合金的凝固组织和性能的影响,探索了原位生成的金属间化合物的存在形式,分析了第二相Bi颗粒的分布.研究结果表明,凝固过程中原位生成的长针状Al_3Ti化合物,均匀分布在Al基体中,穿插在Bi相颗粒之间,阻碍了Bi相颗粒的沉降及凝并,防止了Bi相颗粒的碰撞及长大,制备了Bi相弥散分布在Al基体中的难混溶合金;同时弥散分布在基体中的硬质相Al_3Ti还增强了基体的强度,提高了合金的硬度,使合金表现出优异的耐磨性能.     

PET与SAN/PAN复合膜界面的 FTIR-ATR研究

应用傅里叶衰减全反射红外光谱(FTIR-ATR)技术对聚对苯二甲酸乙二酯(PET)表面形成不同厚度的超薄苯乙烯-丙烯腈共聚物(SAN)和聚丙烯腈(PAN)的共混物膜及其SAN/PAN共混物膜的厚度、界面层PET亚甲基的构像变化等进行研究,结果表明PET表面共混物膜的厚度随共混物混合液中SAN含量的增加而增加,界面层成膜物质与基材的分子链段间发生了相互渗透和扩散,分子链的极性越相近,越容易成膜.对PET红外光谱吸收峰的A1340/A1410进行定量研究表明,在成膜过程中,PET分子链的亚甲基构像由反式向旁式转变,引起界面层PET的结晶度降低.FTIR-ATR是分析复合膜界面层结构信息的有效方法.     

IR-RAS光谱原位研究界面P507分子的存在状态及其变化

采用原位反射红外吸收光谱(IR-RAS)研究了气-液界面P507分子的存在状态及其随水相酸度的变化。结果表明:当水相pH降低时,P507分子极性端基团的质子化状态发生改变。P—O—H和P=O基团峰位向高波数移动,P—O—H吸收峰强度增强。P507分子极性端间的氢键相互作用随质子化程度增加而增强。本文的工作阐明酸性磷类萃取剂分子在油水两相界面处的存在形式及其与水相氢离子的相互作用机制,从而在理论上为指导改进皂化工艺奠定了基础。     

小角X射线散射表征非晶合金纳米尺度结构非均匀

表征纳米尺度结构非均匀对于理解非晶合金的变形、弛豫等动力学行为至关重要.受时空尺度限制,非晶合金纳米尺度结构非均匀的实验表征具有很大的挑战性.本文针对一种典型的锆基非晶合金,开展了同步辐射小角X射线散射原位拉伸实验.通过对散射曲线的定量分析,揭示了非晶合金在纳米尺度的非均匀结构图像.首先,Porod散射曲线呈现正偏离行为,表明非晶合金属于非理想两相散射体系,两相界面弥散且任一相内都存在电子密度涨落.基于散射曲线的Guinier定律分析,进一步揭示非晶合金中散射体形状远偏离球形,其特征尺度主要分布在0.8—1.6 nm之间,且在弹性变形阶段几乎不变.最后,通过Debye相关函数分析,发现这些纳米尺度散射体仅在1 nm之内存在强关联,符合非晶合金短程有序、长程无序的结构特征.研究结果表明非晶合金中存在具有复杂空间分布的纳米尺度非均匀结构.     

酞菁晶体结构与荧光性质的压力调控

酞菁是一种重要的有机光电材料,关于其晶体结构和光电性质间的内在关联尚存争议.本文利用高压原位拉曼散射光谱及荧光光谱技术对酞菁晶体在高压下的结构转变和光学性质进行了研究.当压力达到12.0 GPa时,酞菁分子本身仍保持稳定,没有发生开环反应.酞菁晶体结构在压力作用下由α相逐渐转变为χ相,这一转变在卸压后恢复到初始α相.酞菁的高压荧光光谱研究表明,荧光强度随压力增高而衰减,至3.0 GPa时消失.高压下酞菁分子间所形成的激基缔合物荧光受抑制,而常压下α相酞菁中观察不到的酞菁分子荧光在高压下出现,这可能与酞菁晶体中呈平行排列的分子之间在压力下重叠程度减小有关.     

Al晶界的第一性原理拉伸试验

基于密度泛函理论和局域密度近似的第一性原理方法，进行了Al晶界的第一性原理拉伸试验.得到Al晶界的理论拉伸强度为9.5 GPa，对应的应变为16%.根据价电荷密度、键长和原子构型随应变的变化，我们证实断裂发生在晶界面，其特征是所有界面键的断裂.同时还发现在周围原子键的数目减少的情况下，界面重构的Al-Al原子键具有共价键的性质.因此Al晶界依然保持着较高的界面强度. 关键词： Al晶界 第一性原理拉伸试验 理论拉伸强度     

金属基复合材料原位反应相场模型

原位反应法制备金属基复合材料具有增强体与基体间无杂质、无污染、颗粒分布均匀等优点,已成为制备金属基复合材料的一种重要方法,揭示其动力学机制及规律具有重要的理论及工业价值.然而,原位反应过程具有反应时间短、随机发生、温度高等特点,目前采用原位实验观测其反应过程仍存在较大困难.本文采用相场法模拟金属熔体内的原位反应过程,首先建立了能够描述双束金属熔体界面反应形核的相场模型,并采用该模型模拟了不同参数下相界反应形核过程.结果表明,形核率随着曲率半径及噪声强度的增大而增大,小曲率半径及强噪声条件下新相颗粒尺寸分布更加均匀,形核率随着过冷度的增大而先增大后减小.     

镍基单晶高温合金界面位错网在剪切载荷作用下的演化

运用分子动力学方法,研究了镍基单晶高温合金γ/γ' 相界面错配位错网在剪切载荷作用下的演化特征.结果表明:(100),(110) 和 (111) 三种相界面形成的位错网在载荷作用下有不同形式和不同程度的损伤,其变形和损伤随温度的增加而增加.在相同的剪切载荷和温度作用下,(100) 相界面形成的正方形位错网最稳定. 关键词： 镍基单晶高温合金 界面位错网 分子动力学     

Cu掺杂对高熵合金FeCrVTi相结构的影响

基于CALPHAD方法,建立了高熵合金FeCrVTiCux(x=0-1)的热力学计算模型,对Cu掺杂的高熵合金FeCrVTi相结构和屈服强度进行了讨论分析. 研究发现当x=0时,室温下FeCrVTi的相结构为BCC-A2、LAV-C14和NITI2相. 在815-1380K温度区域,该体系发生有序-无序LAVES->BCC-A2转变. 当x增加到0.2时,室温下FeCrVTiCu0.2的 LAV-C14相消失,出现了LAVES和HCP-A3相. 当x增加到0.4时,室温下FeCrVTiCu0.4出现FCC-A1相. 600K温度时,随Cu含量的不断增加FeCrVTiCux在x=0.0-1.0之间HCP-A3相成分呈线性增长,其相含量最大值位于x=1.0的位置. Cu的掺杂提高了高熵合金FeCrVTi的室温塑性和高温强度,使得FeCrVTi的室温屈服强度高于FeCrVTiCu,在600K温度下,FeCrVTiCu的屈服强度高于FeCrVTi.     

Mechanical modifications in dense polyethylene induced by energetic electron beams

Effects of radiation damage in ultra high molecular weight polyethylene are investigated by using energetic electron beams. Special attention is devoted to the mechanical characterization of the polymer, before and after the modification induced by 5 MeV electrons, as a function of the absorbed dose. Elastic modules, ultimate tensile and compressive strengths and roughness and hardness, have been measured in pristine and electron irradiated polymers. Infrared spectroscopy, scanning electron microscopy and differential scanning calorimetry are employed in order to investigate the microscopic modifications induced by the electron energy release to the polymeric chains. Results indicate that the polymer loses hydrogen and becomes rich in carbon content. Cross-linking effects are responsible for the higher mechanical resistance, fragility and hardness of the polymer submitted to a high absorbed dose.     

Enhancing the Fibre Matrix Adhesion of Natural Fibre Reinforced Polypropylene by Electron Radiation Analyzed with the Single Fibre Fragmentation Test

The effects of electron radiation on natural fibre reinforced polypropylene have been analyzed with the single fibre fragmentation test. Specimens of single hemp, flax, ramie and cotton fibres/fibre bundles embedded in a polypropylene sheet were irradiated with electron radiation of 10 MeV with intensities of 5, 15 and 33 kGy. The radiation led to a strain reduction of the polypropylene but did also improve the adhesion between polymer and flax, hemp and cotton fibres/fibre bundles. The critical fragmentation length and the interfacial shear strength (IFSS) of the composite specimens have been determined showing a clear increase of the IFSS of up to 50% compared to specimens with applied coupling agents. Due to the high strain reduction of the PP at intensities of 15 and 33 kGy the different fibres could only be compared at 5 kGy. The ramie fibre specimens could be analyzed at 5 and 15 kGy intensity showing higher IFSS values at the higher intensity. A possible explanation for the improvement is the forming of radicals with the cellulose chains of the natural fibres and the polypropylene molecules leading to crosslinking and, therefore, better adhesion between the different components.     

Effects of electron-beam irradiation on surface oxidation of polymer composites

The aim of this article was to show the effects of an electron radiation dose and presence of a compatibilizer on the oxidation of composites made of blends of low-density polyethylene (LDPE), high-density polyethylene (HDPE), polypropylene (PP), polystyrene (PS), and poly(ethylene terephthalate) (PET) as well as of blends of LDPE, HDPE, and PP. As the compatibilizers, the styrene-ethylene/butylene-styrene elastomer grafted with maleic anhydride (SEBS-g-MA) and trimethylol propane trimethylacrylate (TMPTA) were used; they were added in the amounts of 5, 10, and 15 wt% and 1, 2, and 3 wt%, respectively. The oxidation of the surface layer (SL) was investigated by the X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). It was found that the extent of the composite oxidation increased with the increasing dose of the electron radiation. The addition of the compatibilizers enhanced the oxidation of the SL but hindered the oxidation of the bulk of the material.     

Effect of gamma irradiation on the thermal,mechanical and structural properties of chlorinated polyvinyl chloride

Non isothermal studies were carried out using thermogravimetry (TG) and differential thermogravimetry (DTG) to obtain the activation energy of decomposition for chlorinated polyvinyl chloride (CPVC) before and after exposure to gamma doses at levels between 5.0 and 50.0 KGy. Thermal gravitational analysis (TGA) indicated that the CPVC polymer decomposes in one main breakdown stage and a decrease in activation energies was observed followed by an increase on increasing the gamma dose. The variation of melting temperatures with the gamma dose has been determined using differential thermal analysis (DTA). Also, mechanical and structural property studies were performed on all irradiated and non-irradiated CPVC samples using stress-strain relations and X-ray diffraction. The results indicated that the exposure to gamma doses at levels between 27.5 and 50 KGy leads to further enhancement of the thermal stability, tensile strength and isotropic character of the polymer samples due to the crosslinking phenomenon. This suggests that gamma radiation could be a suitable technique for producing a plastic material with enhanced properties that can be suitable for high temperature applications and might be a suitable candidate for dosimetric applications.     

电子束辐照对聚碳硅烷结构与热解性能的影响

在惰性气氛下,用电子束对聚碳硅烷(PCS)进行辐照改性。利用傅里叶变换红外光谱分析、凝胶含量测定以及热重-气相色谱-质谱连用技术对不同剂量改性的PCS进行了分析表征,研究了辐照剂量对PCS结构与热解性能的影响。结果表明,电子束辐照作用使PCS样品中大量Si—H键和C—H键发生断裂,形成了以Si—C—Si为骨架的三维网状凝胶产物,当辐照剂量高于3MGy时,PCS的凝胶化程度随辐照剂量的增加而明显变大。热重分析表明,电子束辐照有利于提高PCS的热稳定性,其初始失重温度和陶瓷化产率都会随辐照剂量的增加而升高,其中,经20 MGy辐照后的PCS样品的陶瓷化产率可达87%。此外,对于400℃预处理的PCS样品,在相同吸收剂量下,样品的凝胶质量分数、初始失重温度和最终陶瓷化产率都较未处理的高。     

Effects of gamma radiation treatment and plasticizer on alkaline solid polymer electrolytes

Alkaline solid polymer electrolyte films have been prepared by the solvent-casting method. Gamma radiation treatment and propylene carbonate plastisizer were used to improve the ionic conductivity of the electrolytes at ambient temperature. The structure of the irradiated electrolytes changes from semi-crystalline to amorphous, indicating that the crosslinking of the polymer has been achieved at a dose of 200 kGy. The ionic conductivity at room temperature of PVA/KOH blend increases from 10⁻⁷ to 10⁻³ Scm⁻¹ after the PVA crosslinking and when the plasticizer concentration was increased from 20 to 30%. Paper presented at the International Conference on Functional Materials and Devices 2005, Kuala Lumpur, Malaysia, June 6 – 8, 2005.     

Effect of the degree of crosslinking on the interfacial layer structure of poly(vinyl chloride) dispersed with crosslinked poly(n-butyl methacrylate) particles

The interfacial layer structure of a model incompatible polymer blend system was analyzed using ¹H pulse nuclear magnetic resonance (pulse NMR) spectroscopy. Non-crosslinked and crosslinked poly(n-butyl methacrylate) particles with a mean size of ca. 0.9 μm were prepared by seeded emulsion polymerization, and the degree of crosslinking was varied. The particles were powdered using a freeze-dry method and dispersed in poly(vinyl chloride) by melt blending. Dynamic mechanical analysis indicated that the non-crosslinked particles were completely compatible. In contrast, mutual diffusion of the polymer chains in the crosslinked particles was restricted within the particle/matrix interfacial layer. As a result, an incompatible phase structure in which the crosslinked particles were dispersed in the continuous phase was formed. Pulse NMR analysis indicated that the interfacial layer thickness was in the range of 17–98 nm. The thickness decreased with an increase in the degree of crosslinking in the particles. The interfacial layer thickness in the particles was approximately 10 times larger than that for the incompatible polymer pair. Tensile test results indicated that the elongation at break was dependent on the thickness of the interfacial layer. The yield stress was developed for the particles with high hardness that was independent of the interfacial thickness.     

Ti/4H-SiC肖特基势垒二极管抗辐射特性的研究

本文采用γ射线、高能电子和中子对Ti/4H-SiC肖特基势垒二极管(SBD)的抗辐射特性进行了研究.研究发现对于γ射线和1 MeV电子辐照,-30 V辐照偏压对器件的辐照效应没有明显的影响.经过1 Mrad(Si)的γ射线或者1×l0¹³ n/cm²的中子辐照后,Ti/4H-SiC肖特基接触都没有明显退化;经过3.43×10¹⁴ e/cm²的1 MeV电子辐照后Ti/4H-SiC的势垒高度比辐照前轻微下降,这是由于高能 关键词： 碳化硅 肖特基 辐照 偏压     

Linearity studies of HD-810 dosimeters by light ion beams

Radiochromic films (RCF), also called GafChromic? films, represent a performant material for accurate quantitative radiation dosimetry. Their compositions allow high dose sensitivity and fewer environmental dependence, giving a good feedback to the absorbed dose value and to the active media absorption, turning color upon being irradiated. The RCF take into account their reduced response near the Bragg peak due to a high linear energy transfer (LET). HD-810 GafChromic? films are tissue-equivalent, have easy optical readings and can be employed for ion dosimetry in radio diagnostic and therapy and for industrial applications. Such dosimeters were employed at Tandetron-Nuclear Physics Institute (?e?, Czech Republic) to study the responses of helium, proton and carbon beams, commonly employed in radiotherapy and microelectronics. The sensitivity of the detector is low enough to measure multiple-beam exposures. The induced effects by the ions in the energy range of 600?keV to 2.0?MeV were investigated in terms of optical absorbance, measured in the irradiated active region of the polymer. The employed ion dose range was between 40?Gy and 2.5?kGy. The experimental results show that the absorbance increases with the irradiation time (i.e. with the absorbed dose). The absorbance induced in the radio chromic film was measured at 673?nm, at which is observed the highest sensitivity of the films. Such data, together with the dose linearity and the dependence on the ion stopping power will be presented and discussed.     

Development and application of chip calorimeter as an X-ray detector

Radiotherapy for cancer patients requires accurate measurement of the absorbed dose of radiation in a treatment planning step. Various types of radiation detectors are currently utilized for dose measurement. Among them, calorimeters are known to be the most precise detector for measuring absorbed dose, but their on-site application is limited by the large size of the equipment. We developed a miniaturized chip calorimeter for application as a radiation detector. The calorimetric radiation detector was built using micro/nano fabrication techniques, and consists of an SU-8 photoresist absorber and high-sensitivity vanadium oxide (VO_x) thermistors. The thermistors had a temperature resolution of 135 μK, and the calorimeter showed a thermal conductance of 11 μW/K. The detector was irradiated with various X-ray dose rates from a linear accelerator, and the absorbed dose to SU-8 was measured. The detector responses showed high linearity with dose rates, demonstrating the feasibility of the radiation detector for practical uses.