银/氯化银电极用于监测混凝土中氯离子含量的研究

采用干湿循环渗透法,通过实验室制备的银/氯化银电极来监测混凝土中的氯离子含量,测试了电极的响应性能和长期稳定性,研究了总氯离子含量与自由氯离子含量之间、总氯离子含量与电位之间的关系。结果表明:银/氯化银电极电位能比较好地监测到混凝土中氯离子含量变化的过程,具有良好的长期稳定性能。总氯离子含量随自由氯离子含量的增加而增加,两者之间呈现幂函数的规律。总氯离子含量随电位上升而下降,两者之间呈指数函数的规律。     

不同合成过程对溶胶-凝胶法制备的ZnO/Ag纳米复合材料光催化性能的影响

以乙酸锌、硝酸银为前驱体,二乙醇胺作为稳定剂,利用溶胶-凝胶法分别采用一步法和两步法制备得到ZnO以及ZnO/Ag纳米复合粉体。所有ZnO/Ag复合物中Ag的含量均为3%(摩尔分数)。对所制备样品的结构和光学性质通过XRD、SEM、TEM、XPS、PL、UV-vis进行了表征,进而以甲基橙为模拟污染物进行了光催化测试。结果表明,不同方法制备得到的ZnO/Ag纳米粉体晶粒均匀,无明显团聚现象,面心立方结构的金属Ag吸附在纤锌矿结构的ZnO表面形成异质结。与纯ZnO相比,掺Ag极大地改善了样品在紫外光下的光催化活性。对不同合成工艺的比较表明,用溶胶-凝胶一步法制备的ZnO/Ag复合物的光催化活性最高,经紫外光照射70min可完全降解甲基橙。     

水电站检修场所职业病危害因素调查分析

分类别对水电站检修过程中现场的职业病危害因素进行调查、识别、检测和分析.结果 表明,防腐车间噪声、其他粉尘、氧化锌超标,可进一步通过优化管理措施来缩短接触时长;主厂房噪声、电焊烟尘、二氧化锰超标,可通过优化局部通风系统、增加移动式通风除尘设备和合理安排气刨作业面来改善.     

电流互感器故障分析及诊断

介绍了一起电流互感器故障的现场情况,分析诊断出了故障发生的原因为生产制造过程中,人工操作误差导致二次绕组间绝缘裕度过小,长时间运行后发生绝缘劣化击穿,并给出了预防此类故障的建议.     

Experimental investigation on carbon steel micro-rod machining by LS-WEDT

This article proposed for the first time the method of the low-speed wire electrical discharge turning (LS-WEDT) combined with the multiple cutting strategy to fabricate carbon steel micro-rods. First, the rotating apparatus submerged in working fluid is designed and manufactured to enable the low-speed wire electrical discharge machine to generate cylindrical geometries. Besides, material removal rate, surface roughness, and machining precision of the micro-rod manufactured by the LS-WEDT are, respectively, investigated. Moreover, the surface microstructure and surface chemical reaction of micro-rods are characterized using scanning electron microscopy and energy-dispersive spectroscopy analysis. Experimental results display that the micro-rod of 70?µm diameter and 1000?µm length can be successfully fabricated. More importantly, the mean absolute diameter deviation of the micro-rod fabricated by LS-WEDT is 0.65?µm and the surface roughness is 0.53?µm, which identified the high machining precision and good surface quality of the micro-rod.     

Synthesis of Pt nanocrystals with different shapes using the same protocol to optimize their catalytic activity toward oxygen reduction

Engineering the shape and thus surface structure of Pt nanocrystals is an effective strategy for optimizing their catalytic activities toward various reactions. However, different protocols are typically used to produce Pt nanocrystals with distinctive shapes, making it difficult to directly compare their catalytic activities owing to the complication of surface contamination. Here we demonstrate that Pt nanocrystals with a variety of shapes, including those enclosed with low- or high-index facets, can be synthesized using the same protocol by simply adjusting the concentration of reducing agent and/or the reaction time. Specifically, when the reducing agent was used at a relatively low concentration, Pt truncated cubes, cuboctahedrons, truncated octahedrons, and octahedrons were produced sequentially upon the increase in reaction time. When 67% more reducing agent was used, Pt cubes and concave cubes were obtained consecutively as the reaction time was prolonged. Our quantitative analysis suggests that the diversity of shape and difference in size can be resulted from the difference in reduction kinetics. In evaluating their structure–activity relationship for oxygen reduction, it was established that the high-index facets on Pt concave cubes possessed a specific activity of 6.3 and 1.3 times greater than those of Pt cubes and octahedrons exposed by {1?0?0} and {1?1?1} facets, respectively. This work not only offers a general method for the synthesis of Pt nanocrystals having diverse shapes and thus different types of facets but also highlights the significance of reduction kinetics in controlling the structure evolution of other metal nanocrystals.     

Mechanical Properties and Interlaminar Fracture Toughness of Glass‐Fiber‐Reinforced Epoxy Composites Embedded with Shape Memory Alloy Wires

The effects of the content and position of shape memory alloy (SMA) wires on the mechanical properties and interlaminar fracture toughness of glass‐fiber‐reinforced epoxy (GF/epoxy) composite laminates are investigated. For this purpose, varying numbers of SMA wires are embedded in GF/epoxy composite laminates in different stacking sequences. The specimens are prepared by vacuum‐assisted resin infusion (VARI) processing and are subjected to static tensile and three‐point‐bending tests. The results show that specimens with two SMA wires in the stacking sequence of [GF₂/SMA/GF₁/SMA/GF₂] and four SMA wires in the stacking sequence of [GF₄/SMA/GF₂/SMA/GF₄] exhibit optimal performance. The flexural strength of the optimal four‐SMA‐wire composite is lower than that of the pure GF/epoxy composite by 5.76% on average, and the flexural modulus is improved by 5.19%. Mode‐I and II interlaminar fracture toughness tests using the SMA/GF/epoxy composite laminates in the stacking sequence of [GF₄/SMA/GF₂/SMA/GF₄] are conducted to evaluate the mechanism responsible for decreasing the mechanical properties. Scanning electron microscopy (SEM) observations reveal that the main damage modes are matrix delamination, interfacial debonding, and fiber pullout.

     

Ultraviolet Photoluminescence of Carbon Nanospheres and its Surface Plasmon‐Induced Enhancement

Ultraviolet (UV) light can be used in versatile applications ranging from photoelectronic devices to biomedical imaging. In the development of new UV light sources, in this study, stable UV emission at ≈350 nm is unprecedentedly obtained from carbon nanospheres (CNSs). The origin of the UV fluorescence is comprehensively investigated via various characterization methods, including Raman and Fourier transform infrared analyses, with comparison to the visible emission of carbon nanodots. Based on the density functional calculations, the UV fluorescence is assigned to the carbon nanostructures bonded to bridging O atoms and dangling –OH groups. Moreover, a twofold enhancement in the UV emission is acquired for Au‐carbon core‐shell nanospheres (Au‐CNSs). This remarkable modification of the UV emission is primarily ascribed to charge transfer between the CNSs and the Au surface.     

Facile growth of homogeneous Ni(OH)<Subscript>2</Subscript> coating on carbon nanosheets for high-performance asymmetric supercapacitor applications

The growth of a Ni(OH)₂ coating on conductive carbon substrates is an efficient way to address issues related to their poor conductivity in electrochemical capacitor applications. However, the direct growth of nickel hydroxide coatings on a carbon substrate is challenging, because the surfaces of these systems are not compatible and a preoxidation treatment of the conductive carbon substrate is usually required. Herein, we present a facile preoxidation-free approach to fabricate a uniform Ni(OH)₂ coating on carbon nanosheets (CNs) by an ion-exchange reaction to achieve the in situ transformation of a MgO/C composite to a Ni(OH)₂/C one. The obtained Ni(OH)₂/CNs hybrids possess nanosheet morphology, a large surface area (278 m²/g), and homogeneous elemental distributions. When employed as supercapacitors in a three-electrode configuration, the Ni(OH)₂/CNs hybrid achieves a large capacitance of 2,218 F/g at a current density of 1.0 A/g. Moreover, asymmetric supercapacitors fabricated with the Ni(OH)₂/CNs hybrid exhibit superior supercapacitive performances, with a large capacity of 198 F/g, and high energy density of 56.7 Wh/kg at a power density of 4.0 kW/kg. They show excellent cycling stability with 93% capacity retention after 10,000 cycles, making the Ni(OH)₂/CNs hybrid a promising candidate for practical applications in supercapacitor devices.

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