Endolaryngeal contact pressures

In this work, we present a new method for in vivo endolaryngeal contactpressure measurement with a miniature pressure transducer. Using this methodology, contact pressures can be measured during videoendoscopy at different locations between the artyenoids and also at various locations along the membranous vocal folds. Twenty adults with organic and functional voice disorders and two vocally healthy adults participated as subjects. Endolaryngeal contact pressure measures were made during a series of phonatory tasks varying pitch, loudness, and phonatory onset and offset. Measures were also made during nonphonatory tasks, including throat clearing, coughing, Valsalva maneuvres, and gagging. The most remarkable findings were: (1) interarytenoid contact pressures were considerably greater than intraglottal contact pressures; (2) interarytenoid contact pressures were greater for lower than higher pitches; (3) both interarytenoid and intraglottal contact pressures were remarkably large during hard glottal attack; and (4) overall, the largest endolaryngeal pressures were recorded between the arytenoids, during a thoracic fixation maneuver and during gag reflex.This work was supported in part by Deutsche Forschungsgemeinschaft (He 2869/1-1), by a grant from the “Verein zur Förderung hör-, sprach- und stimmgestörter Patienten an der FU Berlin e.V.” (nonprofit organization), Berlin, Germany, and by Grant No. K08 DC00139 from the National Institute on Deafness and Other Communication Disorders.     

窄带脉冲信号测量横波衰减系数-频率曲线的方法

提出一种测量材料超声横波衰减-频率曲线(α_s-f)的方法:应用窄带脉冲驱动接触式横波探头的脉冲反射方式,采用石英晶体作为耦合块,通过测量耦合块和被测试块耦合界面的声压反射和透射系数,并在衍射修正下测量得到单频率下的超声横波衰减系数;在探头有效带宽内改变发射频率并重复测量,得到不同频率下超声横波衰减系数数值;利用非线性最小二乘拟合方法得到其α_s-f曲线。采用该方法对铝合金6061材料的衰减系数进行测量,得到α_s-f曲线结果为α_s(f,2z)=0.32f2.93,皮尔逊相关系数R为0.9864。测量结果与现有方法所得结果进行对比,本方法在单频率下的结果与现有方法吻合,表明本方法测量的有效性,而多频率测量的方法对研究材料α_s-f关系具有重要意义。     

基于近红外光谱的柔性基底紫外臭氧改性效果表征研究

近年来,随着纳米科技、聚合物材料和先进制造技术的发展,以柔性传感器为代表的新兴柔性电子器件在可穿戴、健康医疗、物联网终端等领域发挥着越来越重要的作用。作为柔性电子器件的载体,柔性基底对传感器的机械可靠性和电学传感性能等方面有着重要的意义。但由于其表面非极性键造成的高疏水性限制了功能性材料在其表面的沉积,常常造成柔性基底层与电极层/敏感层之间不稳定的界面结合。因此,利用紫外臭氧处理对柔性基底表面改性受到了广泛的关注。利用近红外光谱技术对柔性基底的紫外臭氧处理效果进行快速精准评估,旨在从基团分子层面探究其改性效果,在实际应用中是对传统依靠接触角测量评估方法的有效补充。具体而言,对四种常见的柔性基底材料聚二甲基硅氧烷(PDMS)、聚萘二甲酸乙二醇酯（PEN）、聚对苯二甲酸乙二醇酯（PET）和聚酰亚胺（PI）进行了1/2/5/10 min不同时长的紫外臭氧（UVO）改性处理,并利用近红外光谱对其改性效果进行表征研究,最后利用接触角测量方法对上述的表征结果进行了验证分析。近红外光谱分析表明：对于柔性PDMS基底,紫外光能量不足以切断其中的甲基（—CH₃）官能团和（—C—Si—）等化学键,无法引入羟基、羧基等亲水性基团。对于柔性PEN和PET基底而言,紫外臭氧处理的效果要优于柔性PDMS基底,且对柔性PET基底的处理效果要优于柔性PEN基底,其原因可能是PEN基底材料中萘环的双环结构具有很强的紫外光吸收能力,阻隔了380 nm以下的大部分紫外线能量。对于柔性PI基底,紫外臭氧处理可以有效引入羟基（—OH）和羧基（—COOH）等活性基团,且这些官能团的强度和数量随着处理时间的增加而增加,从而在短时间内使得PI基底表面能增大、接触角减小、湿润性提高。接触角测试结果验证：紫外臭氧处理对于柔性PDMS基底处理效果不明显（接触角下降幅度为8.4%）;对柔性PET基底处理的效果（接触角下降幅度为39.6%）要优于柔性PEN基底的处理效果（接触角下降幅度为9.4%）;紫外臭氧处理的效果对柔性PI基底处理效果最佳,接触角下降幅度达到了62.7%。     

Evaluation of surface characteristics under fretting of electrical contacts: Removal behaviour of hot dipped tin coating

The fretting corrosion behaviour of hot dipped tin coating is investigated at low fretting cycles at ±25 μm displacement amplitude, 0.5N normal load, 3 Hz frequency, 45-50% relative humidity, and 25 ± 1 °C temperature. The typical characteristics of the change in contact resistance with fretting cycles are explained. The fretted surface is examined using laser scanning microscope, scanning electron microscope and energy dispersive X-ray analysis to assess the surface profile, extent of fretting damage, extent of oxidation and elemental distribution across the contact zone. The interdependence of extent of wear and oxidation increases the complexity of the fretting corrosion behaviour of tin coating. The variation of contact resistance clearly revealed the fretting of tin coating from 50 to 1200 cycles and the fretting of the substrate above 1200 cycles. The observed low and stable contact resistance region and the fluctuating resistance region at various fretting cycles are explained and substantiated with Scanning electron microscopy (SEM), laser scanning microscope (LSM) and energy dispersive analysis of X-rays (EDAX) analysis results of the fretted surface.     

Weathering of copper-amine treated wood

In this study, the effect of ultraviolet light (UV) irradiation and water spray on color, contact angle and surface chemistry of treated wood was studied. Southern pine sapwood (Pinus Elliottii.Engelm.) treated with copper ethanolamine (Cu-MEA) was subjected to artificially accelerated weathering with a QUV Weathering Tester. The compositional changes and the surface properties of the weathered samples were characterized by Fourier transform infrared (FTIR) spectroscopy, color and contact angle measurements. FTIR indicated that MEA treatment was not found to slow down wood weathering. FTIR spectrum of MEA-treated sample was similar to that of the untreated SP. However, the Cu-MEA treatment retarded the surface lignin degradation during weathering. The main changes in FTIR spectrum of Cu-MEA treatment took place at 915, 1510, and 1595 cm⁻¹. The intensity of the bands at 1510 and 1595 cm⁻¹ increased with the Cu-MEA treatment. Both untreated and MEA-treated exhibited higher ΔE than the Cu-MEA treated samples, indicating that MEA treatment did not retard color changes. However, ΔE decreased with increasing copper concentration, suggesting a positive contribution of Cu-EA to wood color stability. The contact angle of untreated and MEA-treated samples changed rapidly, and dropped from 75 ± 5° to 0° after artificial weathering up to 600 h. Treatment with Cu-MEA slowed down the decreasing in contact angle. As the copper concentration increases, the rate of change in contact angle decreases.     

Modification of surface properties of electrospun polyamide nanofibers by means of a perfluorinated acridine

Polyamide 6 (PA6) nanofibers were prepared from formic acid solutions by using electrospinning technique. The fibers were smooth, defects free and with diameters smaller than 200 nm. Small amounts of a perfluorinated acridine were added as dopant to the feed solution to modify the wettability of the fibers. The effect of doping on the contact angle values is well apparent. The contact angle values go from 50° of pure PA6 to 120° when 6% of acridine is added. A comparison between fibers and films of pure and doped polyamide 6 was carried out in order to determine the effect of morphology on wettability. Thermal annealing near the T_g of the polymer promoted the segregation of the molecules to the surface, reaching contact angles of 131° with smaller amounts (4%) of acridine. The surface segregation was also promoted by time aging.     

超疏水聚合物表面的水滴蒸发模拟

基于质量守恒和Fick第一定律，模拟了水滴在超疏水聚合物表面的蒸发全过程．研究从以往的接触角<90±扩展到>150±，液滴形貌扩展为椭球球帽模型进行疏水表面蒸发模拟．水滴在超疏水PC和FPU/PMMA表面蒸发的实验结果显示，计算的椭球球帽模型可以更好的反映出液滴接触角和高度的变化情况，并且不同聚合物表面接触角的相同变化趋势也揭示出微-纳二级结构表面结构不仅影响液滴接触角，也影响液滴蒸发模式．     

Improvement of water and oil repellency on wood substrates by using fluorinated silica nanocoating

We have investigated a one-step fabrication of fluoro-containing silica coating on wooden substrates, showing multi-functions including super repellency toward water and sunflower oil, low sliding angles, good durability, and low adsorption capacity of moisture. The repellent slurry, consisting of well-mixing silica nanospheres and perfluoroalkyl methacrylic copolymer, is simply prepared and subsequently sprayed over wooden substrates with good adhesion. It has shown that the decoration of silica nanospheres on microscaled wooden texture acts as a crucial role in improving the repellency toward water and sunflower oil droplets. The maximal contact angles can reach as high as 168.3° and 153.6° for water and sunflower oil drops, respectively. These analyses of wetted fraction and work of adhesion also demonstrate the improved repellency due to the addition of silica. This improvement of the repellencies is ascribed to the fact that the drops partially sit on F-coated silica spheres, leaving a layer of air underneath the droplet (i.e., Cassie state). On the basis of the results, the multi-functional coating on wooden substrates delivers a promising commercial feasibility on a variety of woodworks.     

Superhydrophobicity of silica nanoparticles modified with polystyrene

Polystyrene/silica nanoparticles were prepared by radical polymerization of silica nanoparticles possessing vinyl groups and styrene with benzoyl peroxide. The resulting vinyl silica nanoparticles, polystyrene/silica nanoparticles were characterized by means of Fourier transformation infrared spectroscopy, scanning electron microscopy and UV-vis absorption spectroscopy. The results indicated that polystyrene had been successfully grafted onto vinyl silica nanoparticles via covalent bond. The morphological structure of polystyrene/silica nanoparticles film, investigated by scanning electron microscopy, showed a characteristic rough structure. Surface wetting properties of the polystyrene/silica nanoparticles film were evaluated by measuring water contact angle and the sliding angle using a contact angle goniometer, which were measured to be 159° and 2°, respectively. The excellent superhydrophobic property enlarges potential applications of the superhydrophobic surfaces.