波前传感器电铸镍层应力实时检测精度评估

目的 搭建电铸应力实时检测平台，评估其测量精度，并探明电化学沉积过程中镍层平均内应力的变化规律。方法 采用横向剪切波前传感器搭建电铸应力实时检测平台，通过测量在铸层应力作用下电铸基底弯曲的曲率半径，利用Stoney公式计算铸层平均应力。采用参考球面反射镜评估横向剪切波前传感器曲率半径的测量精度，并在0.5 A/dm2电流密度下进行电铸应力实时检测实验，对铸层平均应力测量极限进行评估，同时对检测误差进行分析。结果 横向波前传感器曲率半径测量精度为99.22%，在0.5 A/dm2电流密度下，所搭建的铸层应力实时检测平台可测量的最小厚度为5.1 μm，由曲率测量波动带来的应力检测误差为1.3 MPa。实验测得铸层平均应力随铸层厚度的增加而变大，当铸层厚度达到30 μm左右，铸层平均应力趋于稳定，应力大小为79.7 MPa。同时发现，当铸层厚度小于30 μm时，沿电铸基底长度方向的铸层平均应力明显大于宽度方向铸层平均应力，随铸层厚度的增加，两个方向的应力大小趋于等值。结论 采用横向剪切波前传感器搭建的电铸应力检测平台，能有效对铸层应力进行高精度的实时测量，为精密电铸过程中应力变化规律的研究提供了检测技术基础。     

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。     

Preparation and characterization of polyvinylchloride membrane embedded with Cu nanoparticles for electrochemical oxidation in direct methanol fuel cell

Copper nanoparticles were prepared by the chemical reduction method. These copper particles were embedded into the polyvinylchloride (PVC) matrix as support and used as an electrode (PVC/Cu) for the oxidation of methanol fuel for improving the current response. The PVC/Cu electrodes were characterized by thermal gravimetric analysis (TGA) for thermal stability of the electrode, X-ray diffraction (XRD) for identification of copper nanoparticles in the electrode, Fourier transform infrared spectroscopy (FTIR) to identify the interaction between PVC and Cu and scan electron microscopy (SEM) with EDAX for the morphology of the electrode. The electrocatalytic activity of the electrode was characterized by the cyclic voltammetry, linear sweep voltammetry, and chronoamperometry techniques. An increase in the electrode activity was observed with the increase of copper quantity from 0.18 g (PVC/Cu-0.18 g) to 0.24 g (PVC/Cu-0.24 g) and the maximum was found at 0.24 g of copper in the electrode. Also, it was observed that the electrode achieved the maximum catalytic current in 0.5 mol/L CH₃OH + 1 mol/L NaOH solution. FTIR identified that water molecules, C—H group, copper nanoparticle and its oxide were available in the electrode. SEM images with EDAX showed that copper particles were properly embedded in the polyvinylchloride matrix.     

1-脱氧野尻霉素控释微丸的制备工艺优化及其药动学研究

1-脱氧野尻霉素控释微丸采用挤出滚圆和流化床方法进行制备。首先使用羟丙基甲基纤维素和微晶纤维素等辅料制备分散体、丸芯，再使用羟丙基甲基纳米纤维素邻苯二甲酸酯作为主要包衣材料进行包衣，并装入胶囊。采用SEM观察微丸的微观形态，以及测定其产率、脆碎度、密度、水分含量和粒径分布等物理性质，研究结果显示微丸性质符合中国药典标准规定。在体外释药试验中，溶出介质和放置方式对药物释放无显著影响，释放过程符合Baker-Lonsdale模型。对比研究1-脱氧野尻霉素原料药、分散体微丸和控释微丸在比格犬体内的控释特性，结果表明：与1-脱氧野尻霉素原料药相比，分散体微丸和控释微丸分别使1-脱氧野尻霉素的生物利用度提高了183.37%和243.87%。此外，1-脱氧野尻霉素控释微丸的体内-体外研究的相关性分析可知体外溶出和体内吸收之间呈现良好的线性关系。     

超声促进Ni/Sn固-液溶解行为

钎焊接头的可靠性主要由界面金属间化合物的形貌及接头微观组织决定,超声辅助钎焊过程中母材溶解行为直接影响接头可靠性。为进一步探明超声对Ni-Sn溶解行为的影响,本文采用浸入实验法对比研究了加载超声和无超声辅助下Ni在Sn中的溶解动力学,通过模拟探明了熔池中声压分布规律,观察了Ni-Sn界面微观组织。上述研究表明,超声作用10 s Ni丝的溶解量与不加超声保温5 min的溶解量相当,表明超声能促进Ni在熔融Sn钎料中的溶解。无超声辅助时,随着保温时间的增加,Ni-Sn界面金属间化合物逐渐增厚,阻碍了Ni与Sn 之间的相互扩散；而在超声空化作用下,Ni-Sn界面处于动态非平衡状态,能促进Ni在液态Sn中不断溶解；同时,在声流作用下界面Ni原子快速迁移至Sn中,在随后的冷却过程中析出大量细长棒状的Ni₃Sn₄金属间化合物。     

管电极电解铣削深窄槽流场研究

针对封闭深窄盲槽结构的加工难点,提出了一种管电极电解铣削加工工艺。通过仿真软件对电解铣削过程中的流场进行建模仿真,利用高速摄影仪观测流场分析该方法的可行性。采用外径0.8 mm的管电极在不锈钢上进行电解铣削加工深窄槽试验,研究电解液压强对深窄槽轮廓精度的影响规律,成功加工出槽宽(1±0.05)mm、槽深(2.5±0.05)mm的高精度、侧壁陡直的封闭深窄盲槽。     

Effect of water aging on the mechanical properties of flax fiber/bio-based resin composites

Present work investigates the effect of hydrothermal aging of flax fiber-reinforced bio-based epoxy resin laminates on the mechanical and thermomechanical properties of the composites. Three different types of bio-based resins were used. Plates reinforced with eight layers plain weave flax fibers of 150 g/m², manufactured using Resin Transfer Molding (RTM), compression molding or autoclave technique depends on type of the resin. One dimensional Fickian behavior shows a good fitting to the experimental data derived from weight measurements. The water uptake at the equilibrium state in the case of 60 °C temperature was slightly greater than that at 40 °C. The mechanical properties after hydrothermal aging show a significant reduction and do not return to their initial values even after the drying process. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48787.     

A novel electrochemical aptasensor based on layer-by-layer assembly of DNA-Au@Ag conjugates for rapid detection of aflatoxin M1 in milk samples

Aflatoxin M₁ (AFM₁) is a common toxin in dairy products that causes acute and chronic human health disorders. Thus, the development of a rapid and accurate AFM₁ detection method is of vital importance for food safety monitoring. This work was to develop a novel electrochemical aptasensor for sensitive and specific determination of AFM_1. The dendritic-like nanostructure was formed on the gold electrode surface by layer-by-layer assembly of gold-silver core-shell nanoparticles modified with DNA conjugates. In the presence of AFM₁, the specific recognition between AFM₁ and Apt caused the disassociation of the DNA controlled dual Au@Ag conjugates from the surface of the electrode, causing less methylene blue to bind to the surface and weakening the electrochemical signal. The more AFM₁ there is, the weaker the electrochemical signal. Transmission electron microscope results showed that the successfully synthesized Au@Ag nanoparticles exhibited a core-shell structure with Au as core and Ag as shell, and their average diameter was about 30 nm. Under optimal conditions, the electrochemical aptasensor showed a wide detection ranging from 0.05 ng mL^?1 to 200 ng mL^?1, and a low detection limit of 0.02 ng mL^?1. Moreover, the proposed strategy has been successfully applied to the detection of AFM₁ in cow, goat, and sheep milk samples with satisfactory recoveries ranging from 91.10% to 104.05%. This work can provide a novel rapid detection method for AFM₁, and also provide a new sensing platform for the detection of other toxins.     

Electrochemical performance and modeling of lithium‐sulfur batteries with varying carbon to sulfur ratios

Lithium‐sulfur batteries have attracted much research interest because of their high theoretical energy density and low‐cost raw materials. While the electrodes are composed of readily available materials, the processes that occur within the cell are complex, and the electrochemical performance of these batteries is very sensitive to a number of cell processing parameters. Herein, a simple electrochemical model will be used to predict, with quantitative agreement, the electrochemical properties of lithium‐sulfur cathodes with varying carbon to sulfur ratios. The discharge capacity and the polarization were very similar for the lowest sulfur loadings, while above 23.2 wt% sulfur the gravimetric capacity dropped significantly, and there was an increase in the cell polarization. In addition, a transition in the electrode morphology, from well dispersed to aggregated sulfur at the surface, will be reflected in the change in a critical model parameter demonstrating the sensitivity and functionality of even this simple model in predicting complex behavior in the lithium‐sulfur cells.     

Reactivity of industrial wastes as measured through ICP-OES: A case study on siliceous Indian biomass ash

An untapped source of amorphous SiO₂, industrially generated Indian biomass ash (SA)—90% amorphous, with composition of ~60% SiO₂ and ~20% unburnt carbon—can be used to produce cementitious and alkali-activated binders. This study reports dissolution of amorphous Si from SA in 0.5 mol/L and 1 mol/L aqueous NaOH, with and without added Ca(OH)₂, at SA:Ca(OH)₂ wt% ratios of 100:0, 87.5:12.5, and 82.5:17.5. Monitoring of elemental dissolution and subsequent/simultaneous product uptake by ICP-OES offers an effective process for evaluating utility of industrial wastes in binder-based systems. After 28 days in solution, up to 68% of total Si is dissolved from SA in 1 mol/L NaOH, with values as much as 38% lower in the presence of Ca(OH)₂, due to the formation of tobermorite-like C-S-H. FTIR, ²⁹Si MAS-NMR, and XRD are used to characterize solid reaction products and observe reaction progress. Product chemistries calculated from ICP-OES results and verified by selective dissolution in EDTA/NaOH—namely, Ca/Si of 0.6-1 and Na adsorption of 1-2 mmol/g—are found to be consistent with those indicated by aforementioned techniques. This indicates the efficacy of ICP-OES in estimating product chemistry via such a methodology.