77 resultados para Dynamic Contact Angle


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Polydimethylsiloxane (PDMS) has been widely used as a base material for bio-MEMS/NEMS devices. It is difficult for PDMS to transfer and spread aqueous solution as a kind of highly hydrophobic material. Therefore, surface modification is necessary for PDMS to make it hydrophilic. In this paper, a method of hydrophilization of PDMS surface is proposed. Gold is sputtered to the PDMS substrate by sputter coater in different average thicknesses. Relationship between the average thickness of gold on the PDMS substrate and the contact angle of the surface was studied. It was found that even gold of average thickness less than 1 nm can result in about 25 degrees change of contact angle. AFM is also used to get topographic information of PDMS surface coated with gold. Three cases are classified with different amount of Au: (1) Heterogeneous zone; (2) Transition zone; (3) Film zone. For heterogeneous zone, a simple model about heterogeneous phase wetting is put forward to interpret this phenomenon.

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Models describing wet adhesion between indenters and substrates joined by liquid bridges are investigated. The influences of indenter shapes and various parameters of structures on capillary force are focused. In the former, we consider several shapes, such as conical, spherical and truncated conical indenter with a spherical end. In the latter, the effects of the contact angle, the environmental humidity, the gap between the indenter and the substrate, etc. are included. Different dependences of the capillary force on the indenter shapes and the geometric parameters are observed. Most interesting finding is that applying the present results to micro- and nano-indentation experiments shows the size effect in indentation hardness not produced but underestimated by the effects of capillary force.(4 refs)

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Nano-fibrillar arrays are fabricated using polystyrene materials. The average diameter of each fiber is about 300 nm. Experiments show that such a fibrillar surface possesses a relatively hydrophobic feature with a water contact angle of 142 degrees. Nanoscale friction properties are mainly focused on. It is found that the friction force of polystyrene nano-fibrillar surfaces is obviously enhanced in contrast to polystyrene smooth surfaces. The apparent coefficient of friction increases with the applied load, but is independent of the scanning speed. An interesting observation is that the friction force increases almost linearly with the real contact area, which abides by the fundamental Bowden-Tabor law of nano-scale friction.

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报道了一种高精度测量光纤连接器端面几何参量的自动测量仪。叙述了光纤连接器的端面几何参量的测量原理。由光纤连接器端面形貌和纤芯中心坐标,可以高精度得到曲率半径、顶点偏移量、端面倾斜角和光纤高度等影响连接器性能的关键端面几何参量。该仪器体积小,自动化程度高,用户界面友好,使用方便,可测量物理接触、角度式物理接触等类型的光纤连接器端面几何参量。实际测量证明,该测量仪有很好的重复测量精度。该测量仪与美国Dorc公司ZX-1 mini PMS测量仪和Norland公司NC3000测量仪相比,测量精度水平相当。该仪器

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提出一种基于正切关系和相位调制技术的动态小角度测量方法。使用双棱镜组成干涉测量臂引导两束平行光至分束棱镜处干涉,通过提取携带被测信息的干涉信号的相位实现动态的小角度测量。由于采用位置探测器(PSD)对测量臂中两平行光束的间距进行测量,简化了测量方程,消除了装置中双棱镜必须对称放置的要求。通过正弦地改变半导体激光器的注入电流在时域内实现对干涉信号的相位调制,形成准外差干涉测量模式,提高了光程差的测量精度。实验验证了该方法的可行性,并讨论了影响小角度测量精度的误差因素。研究结果表明,基于该方法的动态小角度的重

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Surface micro-roughness, surface chemical properties, and surface wettability are three important aspects of wafer surfaces during a wafer cleaning process, which determine the bonding quality of ordinary direct wafer bonding. In this study, InP wafers are divided into four groups and treated by different chemical processes. Subsequently, the characteristics of the treated InP surfaces are carefully studied by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and contact angle measurements. The optimal wafer treatment method for wafer bonding is determined by comparing the results of the processes as a whole. This optimization is later evaluated by a scanning electronic microscope (SEM), and the ridge waveguide 1.55 mu m Si-based InP/InGaAsP multi-quantum-well laser chips are also fabricated. (c) 2005 Elsevier B.V. All rights reserved.

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The shape evolution of Ge/Si(001) islands grown by ultrahigh vacuum chemical vapor deposition were investigated by atomic force microscopy at different deposition rates. We find that, at low deposition rates, the evolution of islands follows the conventional pathway by which the islands form the pyramid islands, evolve into dome islands, and dislocate at a superdome shape with increasing coverage. While at a high deposition rate of 3 monolayers per minute, the dome islands evolve towards the pyramids by a reduction of the contact angle. The presence of the atomic intermixing between the Ge islands and Si substrate at high deposition rate is responsible for the reverse evolution. (C) 2001 American Institute of Physics.

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A novel inorganic-organic hybrid hydrophobic anti-reflection silica film used for laser crystal was obtained by sol-gel process. The film consisted of silica sols mixed with a small amount of polymethyl methacrylate (PMMA) or polystyrene (PS). The optical transparency, hydrophobic property and surface morphology of the film were characterized by UV-VIS-NIR spectrophotometer; contact angle instrument and Scanning Electron Microscopy (SEM), respectively. The results showed that the anti-reflection coating had good hydrophobility and optical transparency from 400 nm to 1200 nm. The contact angle reached to 130-140 degrees. SEM images indicated the hydrophobic films modified with PMMA or PS had compact structure compared to the pure silica sol film. (C) 2008 Elsevier B.V. All rights reserved.

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低介电常数材料可作为微电子器件的层间或是导线间的绝缘材料,以提高微电子芯片的信号传输速率。在聚合物材料中引入氟元素或引入空洞可以有效降低聚合物材料介电常数。本文利用层层组装的方法在聚合物中引入空洞以降低聚合物材料的介电常数。这样,不仅能够获得低介电常数材料,而且可以得到超薄膜,对于降低电子元件的尺寸、提高芯片的信号传输速率具有实际的应用价值。 对具有笼状结构的八苯代聚倍半硅氧烷(OPS)采取先用发烟硝酸硝化为带有硝基的产物ONPS,然后再以水合肼作为还原剂将硝基还原为胺基的两步反应方法,制得了带有胺基的聚倍半硅氧烷(OAPS)。用NMR、FTIR方法对合成过程从原料、中间产物、及目标产物进行跟踪分析证明反应结束后,OAPS仍然具有完整的笼状结构,并且胺基化很完全。另外,利用发烟硫酸作为磺化试剂,采用一步合成的方法制得了磺化OPS(SOPS)。经NMR、FTIR表征,确认了SOPS的结构,磺酸基是在苯环上Si的间位发生了取代。经XPS分析得知,OPS上约有91%的苯环参与了磺化反应。在合适的条件下SOPS与OAPS都可以溶于水,分别带有负电荷与正电荷。 然后,利用合成的SOPS与聚丙烯胺(PAH)进行组装。当PAH溶液的pH值小于7.5时,SOPS在PAH溶液中产生脱落现象。通过调节PAH溶液的pH值,可以控制SOPS在PAH溶液中的脱落现象。当PAH溶液的pH值为9.0时,SOPS在PAH溶液中不再脱落。紫外数据表明,尽管组装过程中SOPS在PAH溶液中会有部分脱落,但这并不影响SOPS/PAH复合多层膜的组装。当溶液的pH为3.0时,OAPS溶于水中并带有正电荷。带有负电荷的聚对苯乙烯磺酸钠(PSS)、聚丙烯酸(PAcA)分别与带有正电荷的OAPS实现层层组装。经过QCM、Contact Angle、XPS、UV等方法表征,证明OAPS/PSS与OAPS/PAcA复合多层膜组装过程中生长均匀,并且多层膜厚度可控。用椭圆偏振的方法测得OAPS/PAcA多层膜的折光指数,运用Maxwell方程将其转化为介电常数为2.01,较纯聚丙烯酸的介电常数(2.56)有明显的降低。加热处理OAPS/PAcA多层膜,红外(FTIR)光谱数据显示OAPS与PAcA间发生了交联反应,形成新的酰胺键。紫外可见(UV-Vis)光谱数据也表明,加热后的OAPS/PAcA多层膜在强酸性溶液中的稳定性较加热前的样品有极大的提高。 合成了聚酰胺酸,并将其制成可溶于水的聚酰胺酸三乙胺盐(PAAs)。调节PAAs溶液的pH值为7.5,使之带有负电荷,可以与带有正电荷的OctaAmmonium(OA-POSS)纳米粒子进行组装。QCM数据显示,当OA-POSS的pH为4.5时,PAAs与OA-POSS的组装量相当,组装量比较大。UV-Vis、XPS数据表明,OA-POSS与PAAs可以实现层层组装,并且组装均匀,可控。加热交联后,PAAs能够很容易地转化为聚酰亚胺(PI)。 调节溶液的pH值,使豇豆花叶病毒(CPMV)表面带有负电。以聚阳离子的聚二烯丙基二甲基胺盐酸盐(PDDA)和聚丙烯胺(PAH)作为插层材料可以实现PAAs与CPMV的层层组装,制得复合多层膜[PDDA/CPMV+(PDDA/PAAs)m]n和[PAH/CPMV+(PAH/PAAs)m]n。QCM、UV-Vis数据表明,多层组装膜的厚度可以通过改变[PAH/CPMV+(PAH/PAAs)m]或[PDDA/CPMV+(PDDA/PAAs)m]的组装循环层数进行调节。而且,薄膜中CPMV与PAAs的比例也可以通过改变(PAH/PAAs)或(PDDA/PAAs)的循环个数进行调节。得到组装多层膜后,将其进行加热处理。FTIR数据显示,以PAH、PDDA作为插层所制备得到的CPMV/PAAs复合多层膜经过加热处理后,PAAs向PI的转化非常完全。用椭圆偏振的方法测试加热交联前后的多层膜样品[PAH/CPMV+(PAH/PAAs)m]n的厚度及折光指数,可以得知,加热处理后,薄膜的厚度稍有降低。将折光指数用Maxwell方程转化为介电常数为2.32,这一数值比纯聚酰亚胺的介电常数值(3.40)降低很多,归因于聚酰亚胺中引入带有空洞结构的CPMV,使聚酰亚胺的密度降低,从而降低材料的介电常数。

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超疏水性表面是指水在固体表面的接触角大于150°的表面。这种表面具有很多独特的性质,如防污、防水、自清洁,防腐等。具有良好透光性的超疏水玻璃在很多交通工具如飞机、汽车等挡风玻璃及日常的建筑幕墙玻璃等方面具有广阔的应用前景。制备超疏水表面一般采用两种方法:一种是先在固体表面构建微细结构,再进行低表面能物质修饰;另一种是直接在具有低表面能材料表面构建微细结构。其中构建表面微细结构这一过程使得超疏水材料的制备过程更加繁琐,同时后续步骤有的还需要采用较昂贵的低能表面进行修饰,因而这些方法在实际大规模应用中缺乏可操作性。因此采用简单、快捷的方法直接制备超疏水表面是非常具有研究有意义的。 本文以常见的普通玻璃为基底,通过气液固扩散法,探索了一种采用简单的一步合成法直接在其表面制备出了具有完全疏水性的表面涂层。这种表面由无序排列的甲基硅氧烷聚合物纳米纤维构成,测试的水滴不能在这样的表面进行粘附,具有非常好的疏水性。同时采用FE-SEM、TG-DTA、FT-IR、Contact angle(CA)等手段对制备的涂层表面进行表征并对纳米纤维可能的形成机理进行了探讨,同时对其耐酸碱性、透光性、耐磨性等也进行了初步的研究。采用冷却这种完全疏水的涂层基底从空气中收集水分,发现这种完全疏水的材料比普通的基底材料具有更好的水分收集效率,因而有望将这种材料在除湿机以及空调上得到应用。

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A superhydrophobic surface has many advantages in micro/nanomechanical applications, such as low adhesion, low friction and high restitution coefficient, etc. In this paper, we introduce a novel and simple route to fabricate superhydrophobic surfaces using ZnO nanocrystals. First, tetrapod-like ZnO nanocrystals were prepared via a one-step, direct chemical vapor deposition (CVD) approach. The nanostructured ZnO material was characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD) and the surface functionalized by aminopropyltriethoxysilane (APS) was found to be hydrophobic. Then the superhydrophobic surface was constructed by depositing uniformly ZnO hydrophobic nanoparticles (HNPs) on the Poly(dimethylsiloxane) (PDMS) film substrate. Water wettability study revealed a contact angle of 155.4 +/- 2 degrees for the superhydrophobic surface while about 110 degrees for pure smooth PDMS films. The hysteresis was quite low, only 3.1 +/- 0.3 degrees. Microscopic observations showed that the surface was covered by micro- and nano-scale ZnO particles. Compared to other approaches, this method is rather convenient and can be used to obtain a large area superhydrophobic surface. The high contact angle and low hysteresis could be attributed to the micro/nano structures of ZnO material; besides, the superhydrophobic property of the as-constructed ZnO-PDMS surface could be maintained for at least 6 months. (C) Koninklijke Brill NV, Leiden, 2010

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A facile and effective aqueous chemical synthesis approach towards well control of periodical ZnO textures in large-scale areas is reported, by which considerable adjusting of surface wettability can be realized. With the assistance of polystyrene spheres monolayer template and morphology control agent, we succeeded in preparing a series of ordered ZnO microbowls with different sag height. It was found that the contact angle could be well adjusted by changing geometry of microbowl. Such novel, ordered arrays are expected to exploit the great potentiality in waterproof or self-cleaning micro/nanodevices, and even microfluidic devices. (C) 2010 Elsevier Inc. All rights reserved.

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The experiments regarding the contact angle behavior of pendant and sessile evaporating drops were carried out in microgravity environment. All the experiments were performed in the Drop Tower of Beijing, which could supply about 3.6 s of microgravity (free-fall) time. In the experiments, firstly, drops were injected to create before microgravity. The wettability at different surfaces, contact angles dependance on the surface temperature, contact angle variety in sessile and pendant drops were measured. Different influence of the surface temperature on the contact angle of the drops were found for different substrates. To verify the feasibility of drops creation in microgravity and obtain effective techniques for the forthcoming satellite experiments, we tried to inject liquid to create bigger drop as soon as the drop entering microgravity condition. The contact angle behaviors during injection in microgravity were also obtained.

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We present in this paper results obtained from a parabolic flight campaign regarding ethanol sessile drop evaporation under reduced gravity conditions. Drops are created using a syringe pump by means of injection through a PTFE (polytetrafluoroethylene) substrate. The drops are recorded using a video camera and an infrared camera to observe the thermal motion inside the drop and on the heating substrate. The experimental set-up presented in this paper enables the simultaneous visualization and access to the heat flux density that is transferred to the drop using a heat flux meter placed between the heating block and the PTFE substrate. We evidence original thermal spreading phenomena during the ethanol drop creation on a heated PTFE substrate. The drop exhibits specific behaviour which is discussed here. This work is performed in the frame of a French-Chinese collaboration (project IMPACHT) for future experiments in a Chinese scientific satellite.

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Acetylated corn starches with different degrees of substitution (DS 0.85, DS 1.78, DS 2.89) were synthesized by the reaction of corn starch with acetic anhydride in the presence of acetic acid under varying reaction temperatures. The product was characterized by FTIR spectroscopy, H-1 NMR, X-ray diffraction and contact angle measurement. Acid-base titration and H-1 NMR methods were employed to determine the degree of substitution of product. FTIR spectroscopic analysis showed that the characteristic absorption intensities of esterified starch increased with increase in the degree of substitution, and the characterized peak of hydroxyl group almost disappeared in the spectrum of DS 2.89 acetylated starch. The detailed chemical microstructure of native starch and acetylated starch was confirmed by H-1 NMR, C-13 NMR and C-13-(1) H-1 COSY spectra.