熔模铸件砂眼缺陷分析

阐述了熔模铸造铸件出现砂眼缺陷的特征与出现的部位,分析了砂眼缺陷产生的内、外部原因并提出了相应的对策。结果表明,砂眼是由于型壳内、外部的型砂和/或耐火材料进入型腔形成的,尽量减少影响型壳质量的人为因素,提高型壳质量是防止铸件砂眼最有效的措施。     

飞机蒙皮材料在醋酸钾型除冰液中腐蚀行为研究

目的 评价醋酸钾型除冰液能否用于飞机除冰以及对飞机蒙皮材料腐蚀性的影响。方法 采用AutoLab电化学工作站对飞机蒙皮材料在不同浓度缓蚀剂、无缓蚀剂醋酸钾型除冰液中的干湿交替腐蚀电化学行为进行分析，通过扫描电镜观察其腐蚀前后表面形貌及涂层/基体金属界面形貌。结果 无缺陷飞机蒙皮涂层在除冰液中的阻抗模值高达2.78×1010 Ω?cm2，而缺陷涂层的阻抗模值只有1.72×107 Ω?cm2，说明缺陷破坏了涂层的完整性，降低了涂层的阻抗模值，明显加速了飞机蒙皮材料的腐蚀。带缺陷飞机蒙皮试样经除冰液腐蚀不同周期后的低频区Rct存在较大变化，试样在高浓度无缓蚀剂除冰液中的Rct始终低于在低浓度溶液中的Rct；试验初期，试样在高浓度除冰液中的Rct较大，说明此时缓蚀剂浓度较高，缓蚀作用明显；但随着腐蚀周期的延长，Rct逐渐减小，说明缓蚀剂逐渐失效，高浓度除冰液的腐蚀性逐渐增强并高于低浓度除冰液。腐蚀实验后，飞机蒙皮涂层表面和涂层/基体金属界面处存在一定的腐蚀产物；人造缺陷破坏了涂层的完整性，降低了涂层的结合力，甚至产生局部剥离，造成除冰液浸入，在划痕处发生了较严重的膜下腐蚀。结论 醋酸钾型除冰液对飞机蒙皮材料存在一定的腐蚀性，尤其是当涂层存在缺陷时，腐蚀较为严重。     

尿素高压设备检漏结构设计

尿素高压设备的检漏结构是实时监测介质是否泄露的基本功能单元。高压设备壳体通常采用单层碳钢或多层包扎内衬耐腐蚀性材料的结构,本文依据设备承压壳体不同的结构形式,详细介绍尿素高压设备检漏系统中检漏槽、检漏孔的结构差异和设计制造的特点,作为尿素高压设备检漏结构的设计参考。     

一种新型三苯胺类空穴传输材料的合成与性能研究

以2，7-二碘-9，9-二甲基芴为原料分别经过Buchwald-Hartwig交叉偶联反应、Ullmann反应，对目标化合物9，9-二甲基N2，N7二苯基N2，N7二-对甲苯基-9H-芴-2，7-二胺（d-TPA）进行合成研究。通过¹H NMR、¹³C NMR以及HRMS-ESI等表征方法确定结构的正确性。研究表明：以铜粉为催化剂的Ullmann反应收率为85%，是最高效的合成方法。通过X射线衍射（XRD）测试和循环伏安法（CV）测试，结果表明：该材料为非晶材料，成膜性较好，且目标化合物的HOMO轨道能级值为-5.23 eV，与常用阳极材料ITO功函相近且化学稳定性较好，有利于空穴由阳极向空穴传输层的注入。将目标化合物用作空穴传输材料制备了有机发光二级管（OLED）并进行性能测试表征，结果显示：所得器件的启亮电压为3.8 V，最大发光亮度为21 412 cd/m²，最大电流效率为4.78 cd/A，表明该化合物有望成为一种性能优异的新型空穴传输材料。     

Grain boundary engineering that induces ultrahigh permittivity and decreased dielectric loss in CdCu3Ti4O12 ceramics

Dielectric materials with ultrahigh permittivity are attracting attention due to the increasing demand for these types of materials for microelectronics and energy storage applications. In this work, we successfully synthesized Zn-doped CdCu₃Ti₄O₁₂ (CdCTO) ceramics with low dielectric loss and large permittivity via an ordinary mixed-oxide technique. Remarkably, at a Zn doping level of 0.10, a CdCu_2.9Zn_0.1Ti₄O₁₂ ceramic exhibited both decreased dielectric loss tangent of ~0.058 and large dielectric permittivity > 4.0 × 10⁴, as well as a good frequency stability over a wide frequency range from 40 Hz to 10⁶ Hz. The high dielectric performance was attributed to the enhanced grain boundary resistance and internal barrier layer capacitor (IBLC) effect due to the fine and uniform grains that formed upon Zn doping. The findings reported in this work provide valuable insights into how to simultaneously realize a low dielectric loss and high permittivity in CdCTO and other related dielectric ceramics.     

基于灰色关联分析法探析隧道中深孔楔形掏槽爆破

自动化凿岩设备在中深孔隧道爆破技术可实现机械与自动，精准快速化施工，改善作业环境，提高施工进度。在隧道爆破掘进中，掏槽是关键，它控制爆破效果，决定着经济效益。经过桐梓隧道3#斜井工程实践，基于灰色关联法对大断面中深孔多级楔形掏槽的影响因素做了优势分析；结果表明：五个相关因素中，小掏对掏槽爆破影响最大，超深影响最小，为今后使用XE3C自动化三臂凿岩台车类似工程爆破开挖的掏槽优化提供了较为可靠的理论优化依据。     

Towards impedance-based temperature estimation for Li-ion battery packs

In order to meet the required power and energy demand of battery-powered applications, battery packs are constructed from a multitude of battery cells. For safety and control purposes, an accurate estimate of the temperature of each battery cell is of vital importance. Using electrochemical impedance spectroscopy (EIS), the battery temperature can be inferred from the impedance. However, performing EIS measurements simultaneously at the same frequency on each cell in a battery pack introduces crosstalk interference in surrounding cells, which may cause EIS measurements in battery packs to be inaccurate. Also, currents flowing through the pack interfere with impedance measurements on the cell level. In this paper, we propose, analyse, and validate a method for estimating the battery temperature in a battery pack in the presence of these disturbances. First, we extend an existing and effective estimation framework for impedance-based temperature estimation towards estimating the temperature of each cell in a pack in the presence of crosstalk and (dis)charge currents. Second, the proposed method is analysed and validated on a two-cell battery pack, which is the first step towards development of this method for a full-size battery pack. Monte Carlo simulations are used to find suitable measurement settings that yield small estimation errors and it is demonstrated experimentally that, over a range of temperatures, the method yields an accuracy of ±1°C in terms of bias, in the presence of both disturbances.     

Finite element modeling of resistive surface layers by micro-contact impedance spectroscopy

Micro-contact impedance spectroscopy (MCIS) is potentially a powerful tool for the exploration of resistive surface layers on top of a conductive bulk or substrate material. MCIS employs micro-contacts in contrast to conventional IS where macroscopic electrodes are used. To extract the conductivity of each region accurately using MCIS requires the data to be corrected for geometry. Using finite element modeling on a system where the resistivity of the surface layer is at least a factor of ten greater than the bulk/substrate, we show how current flows through the two layers using two typical micro-contact configurations. This allows us to establish if and what is the most accurate and reliable method for extracting conductivity values for both regions. For a top circular micro-contact and a full bottom counter electrode, the surface layer conductivity (σ_s) can be accurately extracted using a spreading resistance equation if the thickness is ~10 times the micro-contact radius; however, bulk conductivity (σ_b) values can not be accurately determined. If the contact radius is 10 times the thickness of the resistive surface, a geometrical factor using the micro-contact area provides accurate σ_s values. In this case, a spreading resistance equation also provides a good approximation for σ_b. For two top circular micro-contacts on thin resistive surface layers, the MCIS response from the surface layer is independent of the contact separation; however, the bulk response is dependent on the contact separation and at small separations contact interference occurs. As a consequence, there is not a single ideal experimental setup that works; to obtain accurate σ_s and σ_b values the micro-contact radius, surface layer thickness and the contact separation must all be considered together. Here we provide scenarios where accurate σ_s and σ_b values can be obtained that highlight the importance of experimental design and where appropriate equations can be employed for thin and thick resistive surface layers.     

A two-dimensional material for high capacity supercapacitors: S-doped graphene

In this work, sulfur-doped graphene-coated electrodes are prepared by cyclic voltammetry in different potential ranges and different cycles (from 10 to 50) for selective modification of electrodes by different functional groups. The prepared electrodes are characterized by spectroscopic, microscopic and electrochemical methods. In scanning electron microscopic analysis, formation of graphene layers and their porous structure have been determined. Electrochemical impedance spectroscopic and cyclic voltammetric analyses are also used in electrochemical characterization of the electrodes. Then, the prepared sulfur-doped graphene-coated electrodes by using cyclic voltammetry in one-step and low cost are used as electrode materials of supercapacitor for the first time in the literature. Since the mesoporous structure of the electrodes prepared in lower potential ranges increases, specific capacitance of the electrodes increases from 74 to 1833 mF cm⁻² with 10 mA cm⁻² current density. This result shows that specific capacitances of prepared electrodes are higher than those of the electrodes prepared with metal-doped in the literature.     

Pinecone biomass-derived activated carbon: the potential electrode material for the development of symmetric and asymmetric supercapacitors

Activated carbon, from biomass (pinecone), was synthesized by conventional pyrolysis/chemical activation process and utilized for the fabrication of supercapacitor electrodes. The pinecone-activated carbon synthesized with 1:4 ratio of KOH (PAC4) showed an increase in surface area and pore density with a considerable amount of oxygen functionalities on the surface. Moreover, PAC4, as supercapacitor electrode, exhibited excellent electrochemical performances with specific capacitance value ∼185 Fg⁻¹ in 1 M H₂SO₄, which is higher than that of nonactivated pinecone carbon and 1:2 ratio KOH-based activated carbon (PAC2) (∼144 Fg⁻¹). The systematic studies were performed to design various forms of devices (symmetric and asymmetric) to investigate the effect of device architecture and operating voltage on the performance and stability of the supercapacitors. The symmetric supercapacitor, designed utilizing PAC4 in H₂SO₄ electrolyte, exhibited a maximum device-specific capacitance of 43 Fg⁻¹ with comparable specific energy/power and excellent stability (∼96% after 10 000 cycles). Moreover, a symmetric supercapacitor was specially designed using PAC4, as a positive electrode, and PAC2, as a negative electrode, under their electrolytic ion affinity, and which operates in aqueous Na₂SO₄ electrolyte for a wide cell voltage (1.8 V) and showed excellent supercapacitance performances. Also, a device was assembled with poly(3,4-ethylene dioxythiophene) (PEDOT) nanostructure, as positive electrode, and PAC4, as a negative electrode, to evaluate the feasibility of designing a hybrid supercapacitor, using polymeric nanostructure, as an electrode material along with biomass-activated carbon electrode.