凸模糊映射的几种定义及其性质

在已有文献的基础上,介绍了几种常见的凸模糊映射的定义,同时,给出了在可微条件下凸模糊映射的一些性质。并得到了凸模糊映射的等价刻画。     

利用溶胶凝胶法测定Eu3+(Tb3+)和phen共掺杂的杂化材料的特性

合成了一系列Eu^3 (Tb^3 )和phen共掺杂的杂化材料，并对其发光性能进行了考察。在所有样品中除了掺杂浓度为1％的样品外，其余材料均为透明块状且无裂纹。所有材料在紫外灯照射下，发出明亮的红光（Eu^3 掺杂）和绿光（Tb^3＋掺杂）。     

Feature Mapping and Recuperation by Using Elliptical Basis Function Networks for Robust Speaker Verification

The performance of speaker verification systems is often compromised under real-world environments.For example,variations in handset characteristics could cause severe performance degradation.This paper presents a novel method to overcome this problem by using a non-linear handset mapper.Under this method,a mapper is constructed by training an elliptical basis function network using distorted speech features as inputs and the corresponding clean features as the desired outputs.During feature recuperation,clean features are recovered by feeding the distorted features to the feature mapper.The recovered features are then presented to a speaker model as if they were derived from clean speech.Experimental evaluation based on 258 speakers of the TIMIT and NTIMIT corpuses suggest that the feature mappers improve the verification performance remarkably.     

Synthesis of Ca2 ZnSi2O7:Eu phosphor by a modified solid-state reaction and its luminescent properties

This paper reports the detailed preparation and phosphorescence properties of Eu2+-activated Ca2 ZnSi2O7 phosphors by a modified solid-state reaction. Phase-pure crystalline Ca2ZnSi2O7 is obtained at 600℃, a much lower temperature than by conventional solid-state reaction and the preparation process of Ca2ZnSi2O7 is simple. The obtained phosphors showed three emission peaks at 480,580 and 620 nm,respectively. Auxiliary activator R3+(R=Dy, Nd, Tm) would enhance their luminescent properties.     

锌铁氧体纳米颗粒的结构与磁性研究

通过水热法制备了一系列具有不同锌含量的ZnxFe3-xO4(x=0,0.15,0.30,0.40,0.48,0.60,0.70)纳米颗粒,并利用透射电子显微镜、X射线衍射仪、振动样品磁强计、超导量子干涉仪和穆斯堡尔谱仪对其进行研究.所有样品均为尖晶石结构;随着样品中锌含量的增加,其晶格常数随之增加,晶粒尺寸从18 nm减小到9nm.在5 K和293 K时,ZnxFe3-xO4纳米颗粒的饱和磁化强度首先随着Zn含量的增加而增大,并在x=0.4时达到最大,随后随着Zn含量的增加而减小.室温下穆斯堡尔谱的测量结果表明:随着锌含量的增加,谱线由较为标准的六线峰逐渐转变为双峰,且在x=0.60时表现为明显的双峰结构,而大块材料在x=0.80时才有类似结果.饱和磁化强度和居里温度的测量结果表明,这种现象可能是由于样品中纳米颗粒表现出的超顺磁性导致的.此外,还讨论了离子分布对超精细磁场变化的影响,并利用Yafet-Kittel模型对样品的磁性变化进行解释.     

无水溶胶凝胶法制备LiFe1-xCoxPO4/C正极材料及其性能研究

在无水溶胶凝胶法基础上,以Fe3+盐为铁源,添加聚乙二醇-400作为表面活性剂,制备了掺杂钴的LiFePO4/C正极材料(LiFe1-xCoxPO4/C,x=0,0.05,0.1)。并通过XRD、SEM、恒流充放电等方法研究了不同钴掺杂量对LiFePO4/C结构、形貌和电化学性能的影响。     

荷载与环境因素耦合作用下超高性能水泥基复合材料的主要性能(英文)

研究了钢纤维掺量和强度等级对超高性能纤维增强水泥基复合材料(UHPFRCC) 宏观性能的影响及UHPFRCC 在荷载与环境因素耦合作用下的耐久性能. 制备了 3 组不同强度等级(100,150,200 MPa) 和不同纤维掺量 (0%,1%,2%,3%) 的高与超高性能水泥基复合材料,并且测试了其各项力学性能和短期耐久性能. 利用设计的预加载装置,在 UHPFRCC150 试件上施加了应力比为 0. 5 的四点弯曲荷载. 结果表明,随着强度等级的增加,在掺加适量钢纤维掺量的情况下,高与超高性能水泥基复合材料的强度和韧性均明显提高,同时其干燥收缩值降低. 对于加载的试件,钢纤维降低了拉应力对 UHPFRCC 抗氯离子渗透性能的不利影响,并且提高了材料的抗冻融性能.     

形变映射法求Boussinesq方程的显式精确行波解

利用形变映射法，建立Boussinesq方程与三次非线性Klein-Gordon(NKG)方程一类特殊类型解的代数变换关系．根据该关系以及NKG方程的已知解，获得Boussinesq方程系统丰富的显式精确行波解，包括孤波解，周期波解，雅可比椭圆函数解和其他精确解．     

CuO/CeO2复合介孔材料的合成及抗菌性能研究

以三嵌段共聚物 P123为模板,通过溶剂蒸发诱导自组装技术（EISA）,以硝酸铈和硝酸铜为原料,合成CuO/CeO2稀土复合抗菌材料,比较了无机原料摩尔比对产物微观结构和抗菌性能的影响。当CuO/CeO2比例等于0.15∶0.85时,复合材料为固溶体材料,且比表面积最大为125.7 m2·g-1,抗菌缓释时间最长达66 h以上。当氧化铜含量升高后,氧化铜从固溶体中析出,大大缩短了抗菌的缓释时间;当氧化铜含量降低时,复合材料的比表面积随之减少,影响了长效抗菌性能。     

柠檬酸含量对溶胶凝胶自燃烧法制备的钡铁氧体磁性能的影响

BaFe12O19 powders with nanocrystaUine sizes were produced by sol-gel auto-combustion method. The precursors were prepared under the molar ratios of citric acid to the metal nitrate of 0.5, 1.0 and 1.5. Appropriate ethylene diamine （C2H8N2） was added in order to adjust pH of 7. The ions distribution of citric acid at different pH explains the effect of citric acid in the starting solution. The XRD patterns of the as-burnt powders and annealing powders show different phases for different citric acid content. In addition, the lattice constants （a, c） derived from X-ray diffraction pattern were changed from 0.58881 nm to 0.58997 nm and 2.32057 nm to 2.32296 nm respectively. The data from VSM indicated that the powder with high citric acid content took on good magnetic properties. Pure single BaFe12O19 of the specific maximum magnetization M（1 T）≈ 49.73 Am^2/kg, the specific remanent magnetization Mr ≈ 30.77 Am^2/kg and the coercive force He≈ 467 kA/m was produced when the molar ratios of citric acid to the metal nitrate was 1.5.