998 resultados para Langmuir


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The propagation of Langmuir waves in nonisothermal plasmas contaminated by fine dust particles with variable charge is investigated for a self-consistent closed system. Dust charge relaxation, ionization, recombination, and collisional dissipation are taken into account. It is shown that the otherwise unstable coupling of the Langmuir and dust-charge relaxation modes becomes stable and the Langmuir waves are frequency down-shifted.

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The cylindrical Langmuir probe under orbital-limited conditions was used to determine the charge density in a low-density collisional plasma. The Langmuir's theory was applied to both electron and ion saturation currents in their respective accelerating regions. Present study indicates that the length of the probe significantly affects the probe characteristics. A probe of suitable length under orbital-limited conditions may be useful under the experimental conditions where the radius of the probe is much smaller than the Debye lengt.

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We examine the shear-thinning behaviour of a two dimensional yield stress bearing monolayer of sorbitan tristearate at air/water interface. The flow curve consists of a linear region at low shear stresses/shear rates, followed by a stress plateau at higher values. The velocity profile obtained from particle imaging velocimetry indicates that shear banding occurs, showing coexistence of the fluidized region near the rotor and solid region with vanishing shear-rate away from the rotor. In the fluidized region, the velocity profile, which is linear at low shear rates, becomes exponential at the onset of shear-thinning, followed by a time varying velocity profile in the plateau region. At low values of constant applied shear rates, the viscosity of the film increases with time, thus showing aging behaviour like in soft glassy three-dimensional (3D) systems. Further, at the low values of the applied stress in the yield stress regime, the shear-rate fluctuations in time show both positive and negative values, similar to that observed in sheared 3D jammed systems. By carrying out a statistical analysis of these shear-rate fluctuations, we estimate the effective temperature of the soft glassy monolayer using the Galavatti-Cohen steady state fluctuation relation.

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A series of gemini surfactants based on cationic imidazolium ring as polar headgroup, abbreviated as lm-n-lm], 2Br(-) (n = 2, 5, 6 and 12), was synthesized. Their ability to stabilize silver nanoparticles in aqueous media was investigated. The resulting suspensions were characterized by UV-Vis spectroscopy and transmission electron microscopy (TEM). They exhibit specific morphologies by adopting different supramolecular assemblies in aqueous media depending on the internal packing arrangements and on the number of spacer methylene units -(CH2)(n)-]. Individual colloids were extracted from the aqueous to chloroform layer and spread at the air/water interface to allow the formation of well-defined Langmuir films. By analysis of the surface pressure-area isotherms, the details about the packing behavior and orientation of the imidazolium gemini surfactant capped silver nanoparticles were obtained. Morphological features of the dynamic process of monolayer compression at the air-water interface were elucidated using Brewster angle microscopy (BAM). These monolayers were further transferred on mica sheets by the Langmuir-Blodgett technique at their associated collapse pressure and the morphology of these monolayers was investigated by atomic force microscopy (AFM). The number of spacer methylene units -(CH2)(n)-] of the gemini surfactants exerted critical influence in modulating the characteristics of the resulting Langmuir films. (C) 2014 Elsevier Inc. All rights reserved.

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A series of gemini surfactants based on cationic imidazolium ring as polar headgroup, abbreviated as Im-n-Im], 2Br(-) (n = 2, 5,6 and 12), was synthesized. Their ability to stabilize silver nanoparticles in aqueous media was investigated. The resulting suspensions were characterized by UV-Vis spectroscopy and transmission electron microscopy (TEM). They exhibit specific morphologies by adopting different supramolecular assemblies in aqueous media depending on the internal packing arrangements and on the number of spacer methylene units -(CH2)(n)-]. Individual colloids were extracted from the aqueous to chloroform layer and spread at the air/water interface to allow the formation of well-defined Langmuir films. By analysis of the surface pressure-area isotherms, the details about the packing behavior and orientation of the imidazolium gemini surfactant capped silver nanoparticles were obtained. Morphological features of the dynamic process of monolayer compression at the air-water interface were elucidated using Brewster angle microscopy (BAM). These monolayers were further transferred on mica sheets by the Langmuir-Blodgett technique at their associated collapse pressure and the morphology of these monolayers was investigated by atomic force microscopy (AFM). The number of spacer methylene units (CH2)(n)-] of the gemini surfactants exerted critical influence in modulating the characteristics of the resulting Langmuir films. (C) 2014 Elsevier Inc. All rights reserved.

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At the shock velocity range of 7~9km/s, the variations of electron density behind strong normal shock waves are measured in a low-density shock tube by using the Langmuir electrostatic probe technique. The electron temperature, calculated based on Park’s three-temperature model, is used in interpreting the probe current data. The peak electron densities determined in the present experiment are shown to be in a good agreement with those predicted by Lin’s calculation. The experimentally obtained ratios of the characteristic ionization distance to the mean free path of freestream ahead of the shock wave are found to be in a good agreement with the existing experiments and Park’s calculation.

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近年来,Langmuir—Blodgett(LB)薄膜诱导晶体生长的方法引起了人们的极大关注。通过优化LB膜的结构和化学性质可以调控晶体的结构、形貌、取向、晶型。本论文在此领域的主要研究内容如下: (1) 制备了硬脂酸和十八胺两种具有不同结构和官能团的LB膜,然后把这两种膜垂直浸入到中性的甘氨酸溶液中。实验结果表明用不同结构和化学性质的LB膜不仅可以调控晶体的结构、形貌和取向,并且可以在相同的溶液中诱导出不同晶型的晶体。 (2) 制备了Y型硬脂酸LB膜,然后把这种模板以不同的方式浸入到氯化钾溶液中。通过改变LB膜模板在溶液中的放置方式,控制溶液中的诱导成核和自发成核的过程,从而生成不同形貌的氯化钾晶体。 (3)我们研究了不同热力学状态的LB膜诱导五水硫酸铜晶体生长过程。结果表明LB膜即使在液态状态下,仍有诱导晶体生长的能力。且LB膜的热力学状态对晶体的形貌和取向有很大的影响。 另外,我们在以上工作之外,还作了两项其他工作。 (4) 研究了各种羧酸类(甲酸、乙酸、丙酸)、丙酮、醇类(甲醇、乙醇、丙醇、丁醇)对谷氨酸溶液结晶晶型的影响。结果表明:当70°C的谷氨酸饱和溶液快速冷却搅拌到0°C时,有羧酸类物质存在时可以得到β型晶体;而当有酮类、醇类、或无添加剂时在相同条件下得到α型晶体。 (5) 利用LB技术制备了聚苯乙烯和硬脂酸的混合薄膜。实验结果证明PS和SA在混合LB膜中是相分离的。其过程是PS在空气/水界面上首先发生聚集,然后这种聚集的程度随着膜压的增加而增大.并且PS在空气-LB膜界面上在空气/LB膜界面上的聚集程度随着时间仍继续发生改变。

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Langmuir-Blodgett(LB)膜技术由于在电子学、非线性光学以及化学传感器等领域具有潜在的应用前景而引起了人们的研究兴趣,其中它的热稳定性对LB膜的应用领域和范围具有一定的影响。本论文在此领域的主要研究内容如下: 利用LB膜技术分别制备了十八胺及硬脂酸、氘代硬脂酸的多层LB膜,采用变温傅立叶变换红外光谱研究了三种LB膜的相变行为。实验发现:十八胺LB膜在55-75 oC温度区间内发生相变,其CH2对称和反对称伸缩振动频率向高能量区发生明显移动;硬脂酸LB膜在70-80 oC的温度区间内发生了明显的相转变,CH2对称和反对称伸缩振动的强度比在升温过程中也有显著改变;氘代硬脂酸LB膜的相行为发生在65-70 oC的温度区间内。 利用LB膜技术制备了十八铵硬脂酸盐(C18H37NH3+C17H35COO-, ODASA)与十八铵氘代硬脂酸盐(C18H37NH3+C17D35COO-, ODASA-d35) Langmuir-Blodgett (LB)膜,使用变温傅立叶变换红外透射光谱研究了它们的热行为。发现LB膜中十八铵硬脂酸盐分子的两个碳氢链高度有序,然而在十八铵氘代硬脂酸盐LB分子中的来自于十八胺的碳氢链部分无序,即在常温下有一些扭曲构象存在于碳氢链中。而十八铵硬脂酸盐的热稳定性也与十八铵氘代硬脂酸盐的热稳定性有些不同。在十八铵硬脂酸盐LB膜中,碳氢链在85 oC到90 oC的温度区间内发生非常明显的有序-无序变化。而在十八铵氘代硬脂酸盐LB膜中,碳氢链和来自于硬脂酸的氘代的烃链各自呈现出不同的热行为,即:碳氢链在80-90 oC的温度区间发生有序-无序变化,尤其是在80-85 oC的温度范围内这个变化非常显著;而氘代的烃链则在70 oC到85 oC这个较长的温度区间发生缓慢的相变。 分别制备了十八铵十二酸盐 (C18H37NH3+C11H23COO-,ODALA)和十八铵二十四酸盐(C18H37NH3+C23H45COO-,ODATA)LB膜,并用变温傅立叶变换红外透射光谱法研究了十八铵十二酸盐和十八铵二十四酸盐LB膜的热行为,比较了十八铵十二酸盐、十八铵硬脂酸盐和十八铵二十四酸盐这三种双链化合物LB膜的热行为。温度相关的红外光谱显示,这三种物质LB膜的热稳定性取决于碳链的长度。其中,十八铵十二酸盐LB膜在50-65 oC的温度区间内发生相变。对应的,十八铵二十四酸盐LB膜在80-90 oC的温度范围内发生有序-无序变化。令人感兴趣的是,十八铵二十四酸盐LB膜的相变温度与十八铵硬脂酸盐LB膜的相变温度基本一样,都是80-90 oC,也即在十八铵二十四酸盐和十八铵硬脂酸盐两种LB膜中,即使二十四酸取代了硬脂酸对前者的热稳定性的影响非常小。以上结果说明,在双长链化合物中,有效链长度取决于双链中的较短的那个烃链,从而来决定膜的热稳定性。在十八铵二十四酸盐LB膜中,十八胺的全部碳链对膜的热稳定性有贡献,而二十四酸的碳链则只有部分(有效部分)烃链有贡献。 制备了十八胺单层和多层LB膜和粒径为几个纳米的金纳米粒子。由于十八胺在pH值小于10.3的溶液中氨基带正电荷,使其置于金纳米溶胶中,利用带正电荷的十八胺和附着负电荷的金纳米粒子之间的静电作用,使得金纳米颗粒成功地吸附组装到十八胺的有序分子膜中,形成有规律的纳米颗粒层。通过紫外-可见光谱、红外光谱以及扫描电镜观察到,金纳米颗粒通过这种方法能够很好的组装在有机分子膜上,而且由于十八胺LB膜的高度有序性使得金纳米颗粒的组装层有序。而且,不同层数的十八胺LB膜对金纳米粒子呈现出不同的吸附行为。 测量了含微量甲醇(体积分数为0.04%~0.24%)的系列乙醇水溶液的近红外光谱,利用近红外光谱分析建立了预测甲醇含量的定量分析模型。比较了用外部检验法(Test Set-Validation)和交叉检验法(Cross-Validaton)建立的数学模型以及研究了使用外部检验法时校正集和检验集样品数的改变对模型预测结果的影响。结果发现,当校正集样品数为15检验集样品数为6(总样品数为21)时,使用外部检验法建立的数学模型预测结果较好,外部检验与交叉检验的预测均方根误差(分别为RMSEE和RMSEP)都较小(分别为0.0105和0.0115)而且很接近。结果表明,近红外光谱方法简单,准确而且实用。

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Oriented crystallization of CUSO4 center dot 5H(2)O on a Langmuir-Blodgett (LB) film of stearic acid has been studied in the temperature ranges of 73-68 degrees C and 53-20 degrees C, respectively. This is the first time that the LB film at temperature above its melting point has been served as a template to induce nucleation and growth of crystals. The experimental results demonstrated that the LB film in the liquid state has the ability of directing the nucleation and growth of crystals. Moreover, X-ray diffraction patterns of the as prepared crystals revealed that the orientation of the attached crystals on the LB film is affected by temperature greatly.

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Langmuir-Blodgett (LB) film of stearic acid was used as template to induce the nucleation and growth of KCl crystals when the KCl solution was cooled from 50 to 25 degrees C. When the LB film template was vertically dipped into the solution, only induced crystals with (1 1 0) orientation were formed. However, if the template was horizontally placed into solutions, both the induced nuclei at the solution/film interface and spontaneous nuclei formed in solution were simultaneously absorbed onto the LB film, and then grew further to form crystals. X-ray diffraction (XRD) patterns and optical microscopy images showed that the orientation and morphology of the crystals were controlled properly by changing the orientation and position of the LB films in the solutions.

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Langmuir-Blodgett (LB) films of octadecylammonium octadecanoate (C(18)H(37)j7NH(3)(+)C(17)H(35)COO(-),ODASA) and octadecylammonium octadecanoate-d(35) (C18H37+NH3+C17D35COO-, ODASA-d(53)) were prepared and their thermal behaviors were investigated by variable-temperature Fourier transform infrared transmission spectroscopy. It was found that the two hydrocarbon chains of ODASA molecule in LB films are highly ordered while that protonated (H) chain in ODASA-d(35) is partially disordered with some gauche conformers introduced at room temperature.