Elaboration of sponge-like biodegradable cationic particles via double-emulsion solvent evaporation

Researchers work on different optimization methods to come up with preparation methods, which show the desired or targeted outcomes. Moreover, nowadays, research is more focused on developing formulations which contain biodegradable polymers. The objective of the present systematic study was to achieve the abovementioned goals by using a cationic ammonio methacrylate copolymer (Eudragit® RS100). A Double-emulsion solvent evaporation technique was used. This methodology was chosen because the particles formed by this method allow encapsulation of both hydrophilic and hydrophobic active molecules. It also has applications in diverse fields such as drug delivery, food, cosmetics, and pharmaceutical industries.

The aim of this research work was to investigate the influence of various process control parameters, such as stabilizer chemical nature and amount, ultra Turrax® stirring speed and time, the morphology, size, and size distribution of the final dispersions. Then, the prepared particles were characterized using a Scanning Electron Microscope (SEM) and a Laser Diffraction Particle Size Analyzer. This study helped us to know which parameters have a drastic effect on the colloidal properties of the particles.     

Mesoscale Surface Patterning of a Laterally‐Grafted Rod Amphiphile: Rings And Fibers

An aromatic amphiphilic molecule based on branched oligo(ethylene oxide) was synthesized. Evaporation‐driven ring formation and Langmuir–Blodgett films are investigated by utilizing this rigid–flexible block molecule. The size of the rings is strongly dependent on the solvent evaporation rate and the concentration of the molecule. In case of fast evaporation, volcano‐like rings are formed by evaporating solution of high concentration. Perfectly symmetrical rings with diameters in the range of 2–6 μm are obtained by evaporating solution of low concentration. The formation mechanism of the ring is briefly discussed. The molecule at the air–water interface exhibits excellent amphiphilic properties. Upon transferring the monolayer onto solid substrates, AFM revealed the formation of fine and long, straight fibers. By combining the data obtained from the isotherms, AFM, water contact angle measurements, and UV/Vis and fluorescence spectra, the fibers are suggested to be formed by π–π stacking interaction of the aromatic rod segments as the oligo(ethylene oxide) branches are submerged in the water subphase upon compression. The fiber formation is associated with the transformation of the aromatic rod segments from the face‐on conformation to the edge‐on conformation.     

Decomposition of 1,1‐dimethyl‐1‐silacyclobutane on a tungsten filament—evidence of both ring C?C and ring Si?C bond cleavages

The decomposition of 1,1‐dimethyl‐1‐silacyclobutane (DMSCB) on a heated tungsten filament has been studied using vacuum ultraviolet laser single photon ionization time‐of‐flight mass spectrometry. It is found that the decomposition of DMSCB on the W filament to form ethene and 1,1‐dimethylsilene is a catalytic process. In addition, two other decomposition channels exist to produce methyl radicals via the Si? CH₃ bond cleavage and to form propene (or cyclopropane)/dimethylsilylene. It has been demonstrated that both the formation of ethene and that of propene are stepwise processes initiated by the cleavage of a ring C? C bond and a ring Si? C bond, respectively, to form diradical intermediates, followed by the breaking of the remaining central bonds in the diradicals. The formation of ethene via an initial cleavage of a ring C? C bond is dominant over that of propene via an initial cleavage of a ring Si? C bond. When the collision‐free condition is voided, secondary reactions in the gas‐phase produce various methyl‐substituted 1,3‐disilacyclobutane molecules. The dominant of all is found to be 1,1,3,3‐tetramethyl‐1,3‐disilacyclobutane originated from the dimerization of 1,1‐dimethylsilene. Copyright © 2010 John Wiley & Sons, Ltd.     

真空变温薄膜电阻测试仪器的设计与应用

设计了自制真空变温薄膜电阻测试仪器,可以实现粗真空条件下,从室温到300℃的四探针法薄膜电阻测试.该仪器适用于开展薄膜物性与电阻和温度相关的实验,例如,金属与半导体薄膜的温度-电阻特性实验,二氧化钒薄膜热滞效应实验等.     

基于圆盘加载波导的THz分布作用振荡器的数值模拟

 提出了一种新的基于真空电子学的THz源——基于圆盘加载波导的THz分布作用振荡器（EIO）,它由圆盘加载波导输入谐振腔、漂移管和输出腔构成。利用2.5维电磁仿真软件UNIPIC对其进行了模拟研究,结果表明慢波结构的长度、漂移管的长度和输出腔的半径对输出功率和频率产生显著影响。经过最优化设计,在注电压为24.85 kV、电流为20 mA的条件下,仿真得出其中心频率为755.5 GHz、峰值功率为1.322 5 W的THz波。     

无沸腾喷雾冷却技术的研究进展

文中简述了无沸腾喷雾冷却技术近年来国内外的研究进展。着重介绍了关于影响无沸腾区换热各参数的实验研究,如壁面温度、介质体积通量、喷雾流量、喷雾倾角和喷雾高度等,为寻求最佳换热提供了指导。并对无沸腾区的理论研究内容进行了归纳,主要是模拟不同喷雾条件下的换热过程及特性参数(如液膜厚度)的大小和分布,并将理论值与实验数据进行比较分析;总结了影响无沸腾区换热的喷雾特性参数和外部特性。     

高真空多层绝热容器真空丧失后传热研究综述

高真空多层绝热低温容器突然的真空丧失可能会引发重大的安全事故.文中综述了国内外研究者在高真空多层绝热低温容器突然的真空丧失方面的研究成果,并对未来的研究方向进行了讨论和展望.     

Dissipation of a two-mode squeezed vacuum state in the single-mode amplitude damping channel

We explore how a two-mode squeezed vacuum state sechθ e^{a+b+ tanh θ} |00> evolves when it undergoes a singlemode amplitude dissipative channel with rate of decay κ. We find that in this process not only the squeezing parameter decreases, tanh θ → e^-κt tanh θ, but also the second-mode vacuum state evolves into a chaotic state exp{b⁺bln[1 - e^-2κt tanh² θ]}. The outcome state is no more a pure state, but an entangled mixed state.     

GaAs光电阴极激活时Cs的吸附效率研究

从NEA GaAs光电阴极的激活光电流曲线发现,当系统真空度不很高时,在首次Cs激活阶段,表面掺杂浓度较低的阴极材料,其光电流产生需要的时间也较长.同时,随着系统真空度的提高,这种时间上的差异又变得不再明显.该现象表明,Cs原子在阴极表面的吸附效率同表面层掺杂浓度以及系统真空度之间有直接的联系.为定量分析这种关系,本文根据实验数据建立了Cs在阴极表面吸附效率的数学模型,利用该模型仿真的结果同实验现象非常符合.该研究对进一步开展变掺杂阴极结构设计和制备工艺研究具有重要的价值和意义. 关键词： GaAs光电阴极 吸附效率 真空度 表面掺杂浓度     

磁过滤器电流对非晶碳薄膜摩擦学特性影响的研究

研究了过滤阴极真空电弧技术中,不同的磁过滤器电流下(5—13 A),制备的四面体非晶碳(ta-C)薄膜对摩擦学特性的影响.通过对薄膜厚度,薄膜结构以及薄膜表面粗糙度随磁过滤电流的变化结果进行了测试,结果表明,随着磁过滤器电流的增大,薄膜的sp³键含量逐渐减少,表面粗糙度从0.13增大到0.38.磁过滤器电流在5 A时,薄膜的摩擦系数最小约为0.08,当电流增大到7 A时,摩擦系数显著增大,磁过滤器电流从7 A增大到13 A时,薄膜的摩擦系数再次减小约为0.1. 关键词： 四面体非晶碳 过滤阴极真空电弧 磁过滤器电流 摩擦系数