碱铝硅酸盐玻璃化学强化关键影响因素概述

化学强化是一种玻璃机械强度增强方法,适用于异型、超薄、高碱、高膨胀玻璃增强,因新型超薄显示产品的屏幕保护玻璃发展需要,化学强化技术重新在碱铝硅酸盐玻璃品种掀起研究热潮。本文对化学强化本质及铝硅酸盐玻璃在屏幕保护玻璃应用进行了回顾,基于玻璃化学强化的高CS、DOL和低CT诉求,归纳总结了关键影响因素,第1,碱铝硅酸盐玻璃的成分及结构是基础,氧化铝有利玻璃网络孔隙增大创造交换通道,氧化钠或氧化锂是离子交换关键物质;第2,对于玻璃组成和结构设计,要求玻璃网络键合度R=O/Si或O/(Si+Al)满足2.15~2.40,碱金属氧化物质量分数大于13%且膨胀系数大于6×10^-6/℃;第3,在化学强化工艺方面,化学强化温度决定离子扩散系数,化学强化时间决定DOL,一步法仅能获得相对较大的CS,而DOL不很理想,只有两种离子参与交换的二步法才有利于CS和DOL同步提高。     

Computer‐aided design methodology for linearity enhancement of multiwatt GaN HEMT amplifiers using multiple parallel devices

This article presents a design methodology for linearizing GaN HEMT amplifiers based on splitting a large FET into multiple parallel FETs with same total gate periphery and by biasing them individually. By varying the biases, the magnitude and the phase of the IMD3 components at the output of FET changes. A detailed simulation methodology using commercial microwave CAD software is presented. Simulation results show that by biasing one device in Class AB and other(s) in deep Class AB mode, IMD3 components of parallel FETs can be made out of phase to each other leading to cancellation and improvement in linearity. Three prototype circuits were simulated using (a) a single 5 mm FET (1 × 5 mm), (b) two parallel 2.5 mm FETs (2 × 2.5 mm), and (c) four parallel 1.25 mm FETs (4 × 1.25 mm), for a total gate periphery of 5 mm, over the frequency range of 0.8 to 1.0 GHz. IMD3 improvement up to 20 dBc was achieved with the 4 × 1.25 mm circuit when the FET biases were optimized. Measurement results show improvement in linearity up to 20 dBc for 4 × 1.25 mm circuit. The proposed method improves linearity without a substantial penalty on the power consumption and is straightforward to implement.     

Images of a First‐Order Spin‐Reorientation Phase Transition in a Metallic Kagome Ferromagnet

First‐order phase transitions, where one phase replaces another by virtue of a simple crossing of free energies, are best known between solids, liquids, and vapors, but they also occur in a wide range of other contexts, including even elemental magnets. The key challenges are to establish whether a phase transition is indeed first order, and then to determine how the new phase emerges because this will determine thermodynamic and electronic properties. Here it is shown that both challenges are met for the spin reorientation transition in the topological metallic ferromagnet Fe₃Sn₂. The magnetometry and variable temperature magnetic force microscopy experiments reveal that, analogous to the liquid–gas transition in the temperature–pressure plane, this transition is centered on a first‐order line terminating in a critical end point in the field‐temperature plane. The nucleation and growth associated with the transition is directly imaged, indicating that the new phase emerges at the most convoluted magnetic domain walls for the high temperature phase and then moves to self‐organize at the domain centers of the high temperature phase. The dense domain patterns and phase coexistence imply a complex inhomogenous electronic structure, which can yield anomalous contributions to the electrical conductivity.     

Experimental Study on Hybrid Organic Phase Change Materials Used for Solar Energy Storage

The solar energy utilization in built environment has been limited due to its low heat flux, uneven distribution in time and space and temporal difference in day and night. The phase change materials have been used to collect the fluctuant solar energy to form a stable energy source for the terminal equipment of the buildings. In this study, the hybrid organic phase change materials was prepared for the capillary radiant heating system which formed a cascade utilization of solar energy. Firstly, lauric acid and stearic acid were selected as the basic organic phase change materials and the binary equilibrium phase diagram was completed based on the method of step cooling curve according to the experimental tests data. The results showed that the phase transition temperature of the mixed acid at the lowest eutectic point was 31.2℃ and the latent heat value was 264.3 kJ/kg when the mass mixing ratio was 70% for lauric acid and 30% for stearic acid. Secondly, the expanded graphite was used as an additive to enwrap the mixed acid and enhance the heat conductivity. The experimental results showed that when the mass proportion of expanded graphite in the mixed acid was 10%, the mixed acid could be completely enclosed by expanded graphite and the stability of melting and solidification was optimal. Additionally, the phase transition temperature of the hybrid phase change material was 31.5℃ and the latent heat value was 217.4 kJ/kg. The novel hybrid phase change material has a lower eutectic point and a higher latent heat of phase change, so it has a large application space and is quite suitable for the cascade utilization of solar energy with capillary network heating system.     

Experimental Investigation of Heat Storage and Heat Transfer Rates during Melting of Nano-Enhanced Phase Change Materials (NePCM) in a Differentially-Heated Rectangular Cavity

In this work, an experimental study of melting heat transfer of nano-enhanced phase change materials(NePCM) in a differentially-heated rectangular cavity was performed. Two height-to-width aspect ratios of the cavity, i.e., 0.9 and 1.5, were investigated. The model Ne PCM samples were prepared by dispersing graphene nanoplatelets(GNP) into 1-tetradecanol, having a nominal melting point of 37℃, at loadings up to 3 wt.%. The viscosity was found to have a more than 10-fold increase at the highest loading of GNP. During the melting experiments, the wall superheat at the heating boundary was set to be 10℃ or 30℃. It was shown that with increasing the loading of GNP, both the heat storage and heat transfer rates during melting decelerate to some extent, at all geometrical and thermal configurations. This suggested that the use of NePCM in such cavity may not be able to enhance the heat storage rate due to the dramatic growth in viscosity, which deteriorates significantly natural convective heat transfer during melting to overweigh the enhanced heat conduction by only a decent increase in thermal conductivity. This also suggested that the numerically predicted melting accelerations and heat transfer enhancements, as a result of the increased thermal conductivity, in the literature are likely overestimated because the negative effects due to viscosity growth are underestimated.     

槽式太阳能集热管内相变微胶囊悬浮液的热力性能分析

针对传统使用水基和油基的太阳能集热器换热效果低和管壁热应力大的问题，以相变微胶囊悬浮液为工作流体，对抛物型槽式太阳能集热器进行了三维建模。采用蒙特卡罗射线追踪法结合有限容积法和有限元法的方法求解了太阳能集热管的光?热?力耦合问题，采用欧拉?欧拉多相流模型研究了相变微胶囊悬浮液在集热管内的流动换热特性。结果表明，相变微胶囊悬浮液强化了集热管内的对流换热，不仅降低了集热管的沿程壁温，且减少了集热管的周向温差，均化了集热管温度分布。集热管周向等效热应力呈花瓣型分布，对应的5个高温度梯度的位置附近(圆周角θ=5°, 90°, 175°, 225°和315°)出现等效应力局部峰值。吸热管内壁面θ=90°处轴向热应力为压应力，作用于整个管程，而径向热应力和切向热应力为拉应力，主要作用在进出口端。相变微胶囊悬浮液浓度越高，强化换热效果越好，集热管热应力越小，但产生的压降也随之增大。     

退火温度对0Cr25Al5热轧态盘条钢组织及性能的影响

采用显微组织分析和分子动力学模拟等方法研究了退火温度对0Cr25Al5热轧态盘条钢组织及性能的影响。结果发现,晶粒尺寸随温度的升高逐渐增加并趋于稳定,但是断后伸长率和断面收缩率在950 ℃突然大幅度下降。试样组织形貌在800 ℃和950 ℃退火温度下的OM及SEM分析结果未见明显差别。于是使用分子动力学模拟对0Cr25Al5钢三元体系的自由能进行了计算,发现随着B2结构的FeAl或者DO3结构的Fe₃Al有序相尺寸的增大,系统自由能先减小后增大,其最小值随着退火温度的升高向有序相颗粒尺寸减小的方向移动。在1273 K的高温下仍然会保留60 nm左右大小的有序相颗粒。因此,推测0Cr25Al5钢在大于950 ℃的温度范围内韧性下降是由于60 nm左右的B2结构的FeAl或者DO3结构的Fe₃Al有序相造成,与晶粒尺寸无关。因此,针对该钢种应进行低温退火促使基体组织回复以消除缺陷,从而抑制Fe、Al等基体原子的扩散。     

ZK60镁合金表面滚压强化试验研究

试验研究了ZK60镁合金表面滚压加工中工艺参数对试件表面粗糙度、表面形貌、表面残余应力和表层显微硬度的影响,结果表明滚压力和重复滚压次数对试件的表面粗糙度、表面形貌以及表面残余应力和表层硬度影响程度较大,滚压速度影响较小。对精车ZK60镁合金试件进行滚压加工,试件表面粗糙度R a、R z最大减小了50.3%和48.1%;残余压应力最大可达-54.55 MPa;显微硬度从试件表层到内部基体材料逐渐降低,表层硬度值最大为92.83 HV 0.25,比基体材料硬度提高了15.32%。     

Elastic modulus of nanocrystalline cemented carbide

The purposes of this work were to obtain the accurate elastic modulus of the nanocrystalline WC–Co cemented carbides, and to propose the mechanism for the difference of elastic modulus between the nanocrystalline and conventional polycrystalline cemented carbides. The nanocrystalline cemented carbide was prepared by spark plasma sintering (SPS) technique. The conventional polycrystalline cemented carbides were prepared by SPS and sinter-HIP techniques as references, respectively. The sintered cemented carbides were characterized by X-ray diffractometry, scanning electron microscopy and the transmission electron microscopy with precession electron diffraction technology. The elastic modulus was obtained by averaging the values measured with the continuous stiffness measurement method of the nanoindentation technology. The results show that the nanocrystalline cemented carbide has a relatively low modulus, which could be attributed to the more interface area and higher fraction ratio of the hcp cobalt phase caused by the rapid heating and cooling process during SPS.     

Microstructural characteristics of as-forged and β-air-cooled Zr–2.5Nb alloy

Multiple characterization and analysis techniques including electron backscatter diffraction (EBSD), electron channeling contrast (ECC) imaging, transmission electron microscopy (TEM) and microhardness test were jointly employed to investigate microstructural characteristics such as local composition, morphology, grain boundary characteristics and interphase orientation relationship of a forged Zr–2.5Nb alloy before and after β-air-cooling. Results show that the as-forged specimen is composed of equiaxed and lamellar α grains and continuous net-like β-Zr films. After the β-air-cooling, the microstructure of the specimen is featured by basket-weave Widmanstätten structure, in which the inter-α-plate second phases are nanoscale β-Zr. Analyses for crystallographic orientations reveal that the Burgers relationship has been strictly followed during the β→α cooling. Compared to the as-forged specimen, the hardness of the β-air-cooled specimen is higher, which could be attributed to the decreased structural sizes of both α and β phases, and the increased fraction of high angle boundaries as well.