Preparation,structure and microwave dielectric properties of novel La2MgGeO6 ceramics with hexagonal structure and adjustment of its τf value

A novel La₂MgGeO₆ ceramic was synthesized through a solid-state reaction process within a sintering temperature range of 1450–1550 °C. By a combination of X-ray diffraction and Rietveld refinement analyses, the ceramics were found to have a pure hexagonal phase structure belonging to space group R3/146. The scanning electron microscopy images revealed that the ceramic grains were closely connected. The effects of internal (lattice energy, valence bond, and fraction packing) and external factors (density) on the microwave properties of ceramics were also studied. The ceramic exhibited excellent microwave dielectric performances, with a relative permittivity (?_r) of 21.2, a quality factor (Q × f) of 52 360 GHz, and a temperature coefficient of resonant frequency (τ_f) of ?44.2 ppm/°C, when sintered at 1500 °C for 4 h. The τ_f value of the La₂MgGeO₆ ceramic doped with CaTiO₃ could be adjusted to zero. Particularly, 0.2La₂MgGeO₆-0.8CaTiO₃ ceramics have good microwave dielectric properties with τ_f = +2.1 ppm/°C, Q × f = 15 610 GHz, and ?_r = 40.3.     

Research on slag-resistance of ZrN-SiAlON-SiC-C composite refractory in different atmospheres

The ZrN-SiAlON composite powder was synthesized using low-grade zircon and bauxite by carbothermal reduction nitridation at first and then ZrN-SiAlON-SiC-C composite refractory were fabricated with the ZrN-SiAlON powder, SiC particles, and a small amount of Si powder as raw materials and sucrose as the binder. The slag resistance of these composites in O₂, N₂ and Ar atmosphere was investigated by X-ray diffraction, scanning electron microscopy, and energy dispersion spectra. The results show that the pores in the inside of ZrN-SiAlON-SiC-C composite refractory were enlarged in oxygen atmosphere due to oxidation, which leads to the decrease in slag resistance. In argon atmosphere, blast furnace slag destroyed the sintered body of zircon, corundum, and cristobalite with the formation of CaZrO₃, then infiltrated into and filled the pores inside the refractory to form a dense layer, which hindered the further erosion of the blast furnace slag. In the reducing atmosphere, the interfacial energy of the gas-liquid phases became larger due to the reactions between blast furnace slag liquid and the gas, resulting in a larger wetting angle which prevented the erosion.     

针对多种处理痕迹的数字语音取证算法

现有的数字语音取证研究主要集中于对单一的某种操作进行检测，无法对不相关的操作进行判断。针对该问题，提出了一种能够同时检测经过变调、低通滤波、高通滤波和加噪这四种操作的数字语音取证方法。首先，计算语音的归一化梅尔频率倒谱系数（MFCC）统计矩特征；然后通过多个二分类器对特征进行训练，并组合投票得到多分类器；最后使用该多分类器对待测语音进行分类。在TIMIT以及UME语音库上的实验结果表明，归一化MFCC统计矩特征在库内实验中均达到了97%以上的检测率，且在对MP3压缩鲁棒性测试的实验中，检测率仍能保持在96%以上。     

加权信息熵与增强局部二值模式结合的人脸识别

针对人脸识别因光照、姿态、表情、遮挡及噪声等多种因素的影响而导致的识别率不高的问题，提出一种加权信息熵（IEw）与自适应阈值环形局部二值模式（ATRLBP）算子相结合的人脸识别方法（IE （w） ATR-LBP）。首先，从原始人脸图像分块提取信息熵，得到每个子块的IEw；然后，利用ATRLBP算子分别对每个人脸子块提取特征从而得到概率直方图；最后，将各个块的IEw与概率直方图相乘，再串联成为原始人脸图像最后的特征直方图，并利用支持向量机（SVM）对人脸进行识别。在AR人脸库的表情、光照、遮挡A和遮挡B四个数据集上，IE （w） ATR-LBP方法分别取得了98.37%、94.17%、98.20%和99.34%的识别率。在ORL人脸库上，IE （w） ATR-LBP方法的最大识别率为99.85%；而且在ORL人脸库5次不同训练样本的实验中，与无噪声时相比，加入高斯和椒盐噪声后的平均识别率分别下降了14.04和2.95个百分点。实验结果表明，IE （w） ATR-LBP方法能够有效提高人脸在受光照、姿态、遮挡等影响时的识别率，尤其是存在表情变化及脉冲类噪声干扰时的识别率。     

Intercalation structure and toughening mechanism of graphene/urea‐formaldehyde nanocomposites prepared via in situ polymerization

Based on the industrialized graphene (GN) product, a series of graphene/urea‐formaldehyde nanocomposites were synthesized via in situ polymerization by incorporation of silicon coupling agent with terminal amino groups (SA) as the compatibilizer. The results showed that addition of SA coupling agent led to much more efficient grafting of UF molecules on the GN surface with high layer thickness by formation of hydrogen bonding, and thus complete exfoliation and uniform dispersion of GN were achieved for the composites. Compared with neat UF, the addition of 1.0 wt% GN resulted in a roughly 25% increase in tensile strength and 12% increase in impact strength; meanwhile the impact fracture surfaces of the composite showed obvious ductile fracture characteristics, indicating the reinforcing and toughening effect of GN on the UF matrix. With increasing GN content, the storage modulus, glass transition temperature and crosslinking density of UF increased, while the tan δ_max decreased, suggesting that a double crosslinking network structure with GN centered crosslinking point and chemical crosslinking point of UF molecular chains formed, leading to improvement in the stiffness of the composites. The present work showed promising potential for developing high performance UF resin on an industrial scale. © 2017 Society of Chemical Industry     

NH_3-OH体系中共沉淀法同时回收钕铁硼废料中Nd-Pr-Co-Fe

为了避免回收单一钕铁硼废料中有价元素带来的操作复杂和资源浪费等问题,本研究采用共沉淀法共沉淀出钕铁硼废料中的有价元素Me(Nd,Pr,Co,Fe),制备可用于生产再生钕铁硼的原料;根据质量守恒和同时平衡原理,采用MATLAB软件建立Me(Nd,Pr,Co,Fe)-OH--NH3热力学模型,绘制lg[Me]-p H曲线模拟共沉淀工艺,并根据模拟结果确立了共沉淀工艺;模拟和实验的结果表明:根据lg[Me]-p H模拟结果可以确立一步共沉淀法的p H:6~10,Fe3+比Fe2+更易于沉淀完全;在上述条件下获得的共沉淀粉末主相均为Nd,Pr,Co,Fe的化合物,且有价元素的百分比含量均大于99.4%;其中,当p H值在8左右时回收率最高,在该条件下金属元素Me(Nd,Pr,Co,Fe)的沉淀效率分别为:98.7%,99.9%,93.6%,99.9%。该结果也表明共沉淀法工艺不仅高效,而且所制备的共沉淀粉末可以满足制备二次钕铁硼的需要。     

Polyethylene oxide-polypropylene oxide -polyethylene oxide derived porous carbon materials with different molecular weights as ORR catalyst in alkaline electrolytes

Polyethylene oxide (PEO)-polypropylene oxide (PPO)-polyethylene oxide block copolymer having different molecular weights are used as precursors of carbon materials to prepare Hollow -Derivatives carbon material as an electrocatalyst through block copolymer self-assembly. The composition and microstructure of the prepared catalysts are shown by Raman spectroscopy, X-ray diffraction (XRD), Test of nitrogen adsorption and desorption curves, High resolution transmission electron microscopy (HR-TEM) and scanning electron microscopy (HR-SEM). Oxygen was passed into alkaline electrolyte solution until the solution reached saturation state. With molecular weight increasing, the obtained sample gradually changed from block to hollow and spherical. When the molecular weight was 12600 g mol^?1, the evenly hollow carbon nanocages was acquired (C-12600). In O₂ saturated alkaline electrolyte (0.1 M KOH solution), C-12600's limited current density，half-wave potential and initial potential are 5.23 mA cm^?2@0.4 V, 0.72 V and 0.81 V, respectively. And most important is that half-wave potential and onset potential have barely change after 2000 cycles of cyclic voltammetry. As a result, the porous carbon materials exhibited excellent electrocatalytic activity while maintaining high stability in alkaline KOH solution.     

碳纳米管改性聚脲材料的研究

制备了化学改性的碳纳米管,并用喷涂制样的方式制备了碳纳米管改性的聚脲材料。研究了碳纳米管的种类和添加量等因素对聚脲力学性能的影响。结果表明,涂膜的拉伸强度和撕裂强度随着原始碳纳米管含量的增多而降低;而随着改性碳纳米管添加量的增加,涂膜拉伸强度先升高后下降,撕裂强度提高,断裂伸长率降低;且改性单壁碳纳米管对聚脲材料力学性能的增强效果明显优于改性双壁和多壁碳纳米管的。