Anodic dissolution of spongy titanium in ethanol solution for preparation of nano-sized TiO2 powder

Nano-sized TiO₂ powder was prepared by electrochemical dissolution of spongy titanium in an ethanol solution following direct hydrolysis of the electrolyte solution. Characterization of the electrochemical product revealed that Ti(OEt)₄ was formed by anodic dissolution of spongy titanium in ethanol solution. X-ray diffraction and transmission electron microscope were, respectively, used to investigate the structure of TiO₂. This study showed that nano-sized TiO₂ prepared by this method has a structural and thermal stability with a narrow size distribution of 5-10 nm. The optimum electrochemical operating conditions established were a temperature of 333-343 K, current density of 400 A m⁻² and faradaic efficiency of 86%. Experiments showed that this process might be recommended as a promising technique for synthesis of nano-sized powder.     

Synthesis and Characterization of Segmented Block Copolymers Based on Hydroxyl‐Terminated Liquid Natural Rubber and α,ω‐Diisocyanato Telechelics

Summary: Segmented block copolymers, consisting of non‐polar soft segments from hydroxyl‐terminated liquid natural rubber (HTNR) and polar hard segments from α,ω‐diisocyanato telechelics obtained by “criss‐cross”‐cycloaddition, have been synthesized. The block copolymer formation took place under relatively mild reaction conditions at 80 °C in dichloroethane in the presence of dibutyltin dilaurate as a catalyst. The resulting block copolymers were characterized by spectroscopic techniques (¹H NMR, FTIR, UV‐vis spectroscopy) as well as GPC for molar mass determination. The block copolymers were compression molded in a hot stage press, and the resulting samples were characterized by DSC and stress‐strain measurement. The solubility and phase morphology of the materials have also been studied.

Segmented block copolymer from HTNR and α,ω‐diisocyanato telechelics     

孔隙水压力与恒定时间对砂岩变形的实验研究

探讨三峡库水位在145-175 m之间涨落及蓄水时水压对岩（石）体的变形特性影响。以实验为基础,进行了不同轴向应力（1σ=55.54,34.18和12.82 MPa）条件下,周期孔隙水压力（Pmin=2 MPa,Pmax=6 MPa）与上、下限恒定时间（ΔT=120和240 s）作用下砂岩的变形特性实验。通过分析1ε-T与p-T关系曲线和p-1ε滞回曲线,可知：1ε-T砂岩曲线呈连续正弦波形演化,当孔隙水压力加载时,应变减小;上限恒定时,应变持续减小到谷值;卸载时,应变逐渐增大;下限恒定时,应变持续增大到峰值。砂岩p-1ε滞回曲线的2个阶段变化,一是微孔隙压密阶段,未形成明显的滞回曲线;二是孔隙水压力耦合阶段,形成了稳定的滞回曲线,表现形式由疏变密,并且稳定的滞回曲线呈逆时针演化。还对比了不同轴向应力和不同恒定时间条件下,每个p-1ε滞回曲线的四区段（加载段、卸载段、上限恒定段和下限恒定段）的Δε-n关系曲线。     

The role of electrostatic interactions in the mechanism of peptide bond hydrolysis by a Ser-Lys catalytic dyad

General-base catalysis in the active site of serine proteasesis carried out by the imidazole side chain of a histidine. Duringformation of the transition state, an adjacent carboxylic acidgroup stabilizes the positive charge that forms on the general-basecatalyst and as a result contributes several orders of magnitudeto the catalytic efficiency of these enzymes. In the recentlydiscovered family of self-cleaving proteins exemplified by theLexA repressor of Escherichia coli, instead of the imidazoleof a histidine, the active-site general-base catalyst was foundto be the -amino of a lysine. The considerably higher capacityof the lysine side chain for proton acceptance raises interestingquestions concerning the role of electrostatic interactionsin the mechanism of proton transfer by this highly basic group.The negative charge elimination studies described here and theireffects on the k_max and pK of LexA self-cleavage are consistentwith a model in which electrostatic interactions between anacidic side chain and the general-base catalyst form a barrierto proton transfer. The implications are that the -amino group,unlike the imidazole group, is capable of effecting proton transferwithout the intervention of a countercharge.     

Initial density dependence of experimental viscosities and of calculated diffusion coefficients of the binary vapor mixtures methanol-benzene and methanol-cyclohexane

The paper reports experimental results for the viscosity of the vapor mixtures methanol-benzene (five mole fractions with densities up to 1.5kg·m^–3 and 0.022 mol·L ^–1) and methanol-cyclohexane (four mole fractions with densities up to 1.9kg·m^–3 and 0.026 mol·L ^–1). In analogy to the pure components, the measurements on the mixtures were carried out with an oscillating-disk viscometer with small gaps, completely made of quartz, beginning as near as possible to room temperature and continuing to a maximum temperature of 630 K. A first evaluation by means of the Chapman-Enskog theory of dilute gases has shown differences in the resulting values of the interaction viscosity _ij ⁽⁰⁾ in the limit of zero density exceeding the experimental errors. Consistent results were obtained by taking into account the initial density dependence of the viscosity within the framework of the modified Enskog theory for gaseous mixtures. The values of _ij ⁽⁰⁾ were also used to estimate binary diffusion coefficients of the mixtures.     

Near infrared light-induced disassembly of polymeric micelles based on methylene blue conjugated polyethylene glycol

Light-sensitive drug delivery systems are considered ideal for applications in the biomedical fields for their ability to release the payload in an on-demand spatiotemporal controlled manner through the manipulation of the light source. Among the broad radiation spectrum, near infrared (NIR) light is considered advantageous compared to UV and visible light, due to its inherently lower photodamage to normal tissues and deeper penetration to lesion areas. In this study, we report a successful synthesis of a polymer capable of undergoing partial degradation upon irradiation with NIR light by conjugating 10-N-carbamoyl linkage methylene blue (MB) moiety, a NIR photocleavable ligand, with polyethylene glycol (PEG). Through effective coupling of MB, a hydrophobic moiety, to the hydrophilic PEG molecule, an amphiphilic polymer was synthesized, as demonstrated by a lowered surface tension (55 mN/m at 0.1% wt/vol). Subsequently, photo-induced reversal of surface activity associated with self-assembled structure disruption, was displayed by surface tension measurements, size distribution analysis, and burst release profile of paclitaxel (PTX) from polymeric micelles upon the exposure to NIR irradiation.     

Micro cam system driven by electrostatic comb-drive actuators based on SOI-MEMS technology

Microsystem Technologies - This paper reports a design and fabrication process of a micro cam system (MCS) with a flat-faced translating follower. The cam rim with cover diameter of 2.4 mm...     

基于抽象和组合方法的网络协议验证

由于模型检测存在状态爆炸问题,多主体的网络协议组合模型检测往往难以进行。为了缓解该问题,分析了通信主体数量增加对状态数量的影响,提出了组合式的抽象验证方法。首先根据所需验证的LTL性质,建立各个通信主体的Kripke结构,再对该Kripke结构进行抽象;然后组合抽象模型;最后运用Spin对组合抽象模型进行检验。为验证该方法的有效性,对NSPK协议进行了检测,结果表明,该方法所需的状态空间向量长度、搜索深度、存贮和遍历的状态数都有明显减少,有利于缓解状态爆炸问题。     

基于事件逻辑的改进Needham-Schroeder协议安全性证明

安全协议是现代网络安全的基础,密码协议的安全性证明是一个挑战性的问题。事件逻辑是一种描述分布式系统中状态迁移的形式化方法,用于刻画安全协议的形式化描述,是定理证明的基础。用事件序语言、事件类和一个表示随机数、密钥、签名和密文的原子类,给出身份认证协议可以被形式化定义和强认证性证明理论。利用该理论对增加时间戳的Needham-Schroeder协议安全性进行证明,证明改进的Needham-Schroeder协议是安全的。此理论适用于类似复杂协议形式化分析与验证。