不同衬底和CdCl2退火对磁控溅射CdS薄膜性能的影响

在科宁7059玻璃, FTO, ITO, AZO四种衬底上磁控溅射CdS薄膜, 并在CdCl₂+干燥空气380 ℃退火, 分别研究了不同衬底和退火工艺对CdS薄膜形貌、结构和光学性能的影响. 扫描电子显微镜形貌表明: 不同衬底原位溅射CdS薄膜的形貌不同, 退火后相应CdS薄膜的晶粒度和表面粗糙度明显增大. XRD衍射图谱表明: 不同衬底原位溅射和退火CdS薄膜均为六角相和立方相的混相结构, 退火前后科宁7059玻璃, FTO, AZO衬底上CdS薄膜有 H(002)/C(111) 最强衍射峰, ITO衬底原位溅射CdS薄膜没有明显的最强衍射峰, 退火后出现 H(002)/(111) 最强衍射峰. 紫外-可见分光光度计分析表明: AZO, FTO, ITO, 科宁7059玻璃衬底CdS薄膜的可见光平均透过率依次减小, 退火后相应衬底CdS薄膜的可见光平均透过率增大, 光学吸收系数降低; 退火显著增大了不同衬底CdS薄膜的光学带隙. 分析得出: 上述结果是由于不同衬底类型和退火工艺对CdS多晶薄膜的形貌、结构和带尾态掺杂浓度改变的结果. 关键词： CdS薄膜 磁控溅射 退火再结晶 带尾态     

Scholte波与含泥沙两相流介质属性关系的分析及仿真验证

基于四种超声悬浮液模型Urick, Urick-Ament, HT, Mcclements分析了Scholte波在两相流体与多孔介质固体界面处的传播特性. 结合各模型的复波数表达式建立含泥沙流体-多孔介质固体界面波特征方程, 分析了Scholte波速与两相流体积含量、粒径等介质属性的关系. 通过仿真实验获得界面波信号, 运用时延估计获得Scholte波速与泥沙含量、粒径的关系, 发现所得的波速与Urick-Ament和HT理论有相对好的一致性. 关键词： Scholte波 两相流体 多孔介质 泥沙含量     

Detecting community structure using label propagation with weighted coherent neighborhood propinquity

Community detection has become an important methodology to understand the organization and function of various real-world networks. The label propagation algorithm (LPA) is an almost linear time algorithm proved to be effective in finding a good community structure. However, LPA has a limitation caused by its one-hop horizon. Specifically, each node in LPA adopts the label shared by most of its one-hop neighbors; much network topology information is lost in this process, which we believe is one of the main reasons for its instability and poor performance. Therefore in this paper we introduce a measure named weighted coherent neighborhood propinquity (weighted-CNP) to represent the probability that a pair of vertices are involved in the same community. In label update, a node adopts the label that has the maximum weighted-CNP instead of the one that is shared by most of its neighbors. We propose a dynamic and adaptive weighted-CNP called entropic-CNP by using the principal of entropy to modulate the weights. Furthermore, we propose a framework to integrate the weighted-CNP in other algorithms in detecting community structure. We test our algorithm on both computer-generated networks and real-world networks. The experimental results show that our algorithm is more robust and effective than LPA in large-scale networks.     

Chaos in social learning with multiple true states

Most existing social learning models assume that there is only one underlying true state. In this work, we consider a social learning model with multiple true states, in which agents in different groups receive different signal sequences generated by their corresponding underlying true states. Each agent updates his belief by combining his rational self-adjustment based on the external signals he received and the influence of his neighbors according to their communication. We observe chaotic oscillation in the belief evolution, which implies that neither true state could be learnt correctly by calculating the largest Lyapunov exponents and Hurst exponents.     

Compositional Dependence of Static Shear Viscosity of Immiscible PP/PS Blends

Phase structures of immiscible polypropylene (PP)/polystyrene (PS) blends with different volume proportions, PP90/PS10, PP80/PS20, PP70/PS30, PP60/PS40, PP50/PS50, PP40/PS60, PP30/PS70, PP20/PS80, PP10/PS90, were observed by means of scanning electronic microscopy (SEM). The zero shear viscosities of the blends were determined according to a modified Carreau model by fitting the curves of static shear rate sweeps of blends tested at 190°C in a Stress Tech Fluids Rheometer. The results showed that the compositional dependence of zero shear viscosity of PP/PS deviated greatly from linear or log‐linear additivity. When PS was dispersed in a PP continuous phase, the blends showed negative deviation, while for blends with PP dispersed in a PS matrix, positive deviation was generated. When different theoretical equations of Nielsen, Utracki, Taylor, Frankel‐Acrivos (FA), Choi‐Schowalter (CS), and Han‐King (HK) were used to fit the experimental data of zero shear viscosities of blends, none of them was suitable for PP/PS blends. These experimental phenomena may result from the complex phase structures of the blends and their response to shear conditions, which are discussed in detail and compared with the experimental analysis.     

Precursor Based on Polyborylborazine for BN Fiber: Preparation and Rheology Properties

A polyborylborazine precursor for hexagonal boron nitride (h-BN) was obtained by reaction of boron trichloride with methylamine and its structure was characterized by ¹¹BNMR, ¹³CNMR, ¹HNMR, and FTIR. The results show that the molecular precursor consists of borazine rings connected via a cross-linked network. The results of shear rheological tests indicated that the polymer is capable of being melt spun at moderate temperature, which implies that the structure of the molecular chains of the precursor polymer is branched. The precursor polymer was spun into a continuous polymer fiber in the melt state and then subsequently heat-treated under NH₃ up to 1000°C for conversion into BN fibers. Its surface morphology was observed by scanning electron microscopy (SEM); the fiber was free of defects and cavities.     

Influence of Bovine Bone Content on In Vitro Degradation of Poly-L-lactic Acid and Bovine Bone Composite Materials

In vitro degradation experiments of poly-L-lactic acid (PLLA) and bovine bone (BB) composites were carried out in a phosphate-buffered solution (PBS) at 37°C with a pH of 7.4. The influence of BB content on pH value of PBS, water uptake, molecular weights, molecular weight distributions, weight losses, mechanical strengths, and morphologies of PLLA/BB was investigated with degradation times. The results indicated that the presence of the BB modified the degradation of the PLLA matrix. The degradation rate of PLLA in the PLLA/BB composite was slower than the degradation rate of the sole PLLA material. Furthermore, the degradation rate of the composites became slower with the increasing content of BB in PLLA/BB composites.     

Study on the Molecular Mobility in the Polyamide/SrFeO Composites by In Situ Infrared Spectroscopy

Polyamide 6(PA6) and its composite with strontium ferrite (SrFeO) magnetic powders at different concentration levels (33%, 80%) are in situ investigated by temperature-dependent Fourier transform infrared spectroscopy (FT-IR). It is found that the intensity changes of the “free” (nonhydrogen bonded) N?H stretching vibration as a function of temperature can be used to determine the glass transition (T _g) and melting temperature (T _m); whereas the hydrogen-bonded N?H stretching vibration is only sensitive to T _m. Our results reveal that high SrFeO contents increase the T _g and T _m of PA6. These observations suggest that the molecular chains of PA6 are confined with increasing content of SrFeO.     

Microstructure,Rheology, and Potential Oil Absorbency of Poly(Butyl Methacrylate) and Poly(Hydroxyethyl Methacrylate) Blends

To prepare oil-absorptive polymers with moderate cross-linking structure, poly(butyl methacrylate) (PBMA) was synthesized as a linear hydrophobic polymer by suspension polymerization. In addition, hydroxyethyl methacrylate (HEMA), as a monomer, which could construct a network structure among the macromolecules via hydrogen bond interactions, was solution polymerized in dimethylacetamide (DMAc) with PBMA, yielding a polymer blend of PBMA and PHEMA. The solution of the polymer blend was investigated by rotational viscometry and extended rheometry. The results showed that the viscosity varied greatly with the temperature and shear rate for three different compositions. Fourier transform infrared (FTIR) spectra indicated that an entanglement or interlocking cross-linking structure of molecular chains was constructed by hydrogen bonds. The results from nuclear magnetic resonance (NMR) spectra exhibited a downfield movement of the proton peak as influenced by end groups or hydroxyls in the polymer chains. The rheological measurements demonstrated that the cross-linking structure greatly affected the rheological behavior of the blend solution. In addition, the cross-linking structure was also evaluated by oil absorbency of films.     

Preparation and Flammability of a Flame-Retardant Poly(Butyl Acrylate-Vinyl Acetate) System Based on Gemin-Surfactant Modified Montmorillonite and Ammonium Polyphosphate

Gemin-surfactant modified montmorillonite (G-MMT) was successfully prepared by an ion exchange reaction and characterized via Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The P(BA-VAc)/G-MMT emulsion was prepared via an in-situ polymerization method using potassium persulfate (K₂S₂O₈, KPS) as an initiator. Ammonium polyphosphate (APP) was introduced for obtaining P(BA-VAc)/APP/G-MMT flame-retardant latex with a constant total content of 15 wt% of APP and G-MMT in P(BA-VAc). The flame retardancy and thermal behavior of the latex films were investigated by limiting oxygen index (LOI), vertical burning test (UL-94) and thermal gravimetric analysis (TG/DTA). Compared with the P(BA-VAc)/APP composite, the LOI value of P(BA-VAc)/APP/G-MMT containing 0.5 wt% G-MMT at the same total additive loading increased to 29.1 from 20.0 and its UL-94 increased from no rating to V-0. Thermal gravimetric (TG) data showed that the amount of residues increased significantly with the loading of G-MMT. In addition, the LOI values increased with the increase in char residues. The morphology and microstructure of the residues generated during LOI testing were investigated by scanning electron microscopy (SEM). The outer surfaces of P(BA-VAc)/APP/G-MMT charred layers were more continuous and compact than those of P(BA-VAc)/APP.