Synthesis,characterization, and redox and electrochromic behaviors of poly(3-n-octyloxythiophene)

Poly(3-n-octyloxythiophene), a conjugated polymer, which possessed solubility in common organic solvents, was synthesized by electrochemical polymerization in the presence of lithium perchlorate as the supporting electrolyte and sodium dodecyl sulfate as the surfactant in an aqueous medium. Characterizations of the intermediate, monomer, and polymer were performed by NMR spectroscopy, Fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy, and gel permeation chromatography. The process of electrochemical polymerization and the electrochemical redox behaviors were investigated by cyclic voltammetry and the potentiostatic method. A poly(3-n-octyloxythiophene) film that was deposited on a platinum electrode was found to exhibit electrochromic behaviors, and it switched electrochemically between blue–green oxidized and dark red reduced states. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Isobaric vapor–liquid equilibria for mixtures of tetrahydrofuran, 2-propanol, and 2,2,4-trimethylpentane at 101.3 kPa

Vapor–liquid equilibrium (VLE) at 101.3 kPa have been determined for a ternary system (tetrahydofuran + 2-propanol + 2,2,4-trimethylpentane) and its constituent binary systems (tetrahydrofuran + 2-propanol, tetrahydrofuran + 2,2,4-trimethylpentane, and 2-propanol + 2,2,4-trimethylpentane). The activity coefficients of liquid mixtures were calculated from the modified Raoult's law. Thermodynamic consistency tests were performed for all VLE data. The VLE data of the binary mixtures and ternary mixtures were correlated using the Margules, Wilson, NRTL, and UNIQUAC activity-coefficient models. The models with their best-fitted interaction parameters of the binary systems were used to predict the ternary vapor–liquid equilibrium. All VLE data are also used to calculate the reduced excess molar Gibbs free energy g^E/RT and the deviations in the boiling point ΔT. The calculated quantities of g^E/RT and ΔT were fitted to variable-degree polynomials in terms of liquid composition.     

Stability of Mixtoxantrone Hydrochloride in Solution

A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of mitoxantrone HC1 and its degradation products under accelerated degradation conditions. The degradation kinetics of mitoxantrone HC1 in aqueous solution over a pH range of 1.18 to 7.20 and its stability in propylene glycol-or polyethylene glycol 400-based solutions were investigated. The observed rate constants were shown to follow apparent first-order kinetics in all cases. The pH-rate profile shows that maximum stability of mitoxantrone HC1 was obtained at pH 4.01. No general acid or base catalysis from acetate or phosphate buffer species was observed. The catalysis rate constants on the protonated mitoxantrone imposed by hydrogen ion water and hydroxy ion were determined to be 3.72 × 10 min^-1 5.64 × 10-min^-1 and 1.108 × 10^-2min^-1, respectively. The degradation rate constants of mitoxantrone affected by different ionic strength systems. Irradiation with 254 nm UV light at 25±0.5°C was found when canpared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol in the pH 4.01 mitoxantrone solution shows an increase in its stability at 502±0.5°C.     

Energy efficiency in cloud computing based on mixture power spectral density prediction

Due to the budget and environmental issues, adaptive energy efficiency receives a lot of attention these days, especially for cloud computing. In the previous research, we developed a combined methodology based on nonparametric prediction and convex optimization to produce proactive energy efficiency-oriented solution. In this work, the predictive analysis was further enhanced by deriving the mixture power spectral density to model the complex cloud monitoring statistics. By engaging the improved technique to the predictive analysis, the prediction process was more adaptive to handle the fluctuation in system utilization. As a consequence, the optimization process could subsequently produce more appropriate setting for energy savings. After the infrastructure setting has been made available, the instruction of virtual machine migration was created and implemented by the cloud orchestrator. This instruction condensed the services into the pool of active facilities, satisfying the objective of power efficiency. Eventually, any physical machine out of the power configuration would be gradually terminated. Compared to our former method, the effectiveness of the proposed technique has been proven by cutting down 4.92% of energy consumption, while still maintaining a similar quality of services.

     

Performance implications of internet channels in financial services: A comprehensive perspective

Advances in information technology (IT) have forced financial services firms to explore new organizational forms and deliver service innovation. Given the obvious differences in the business model in which the financial services sector provides online services, it is natural to ask whether the emergence of Internet channels leads to superior achievement. Using a sample of twenty-four Taiwanese publicly traded financial services firms from 1997 to 2003, this empirical study attempts to assess the Internet channel??s effect on firm performance by means of applying event study methodology and data envelopment analysis. Results show that the magnitudes of average abnormal returns are uniformly positive and increase the operating efficiency of firms following announcements via Internet channels. This work therefore concludes that Internet channels have positive influences on firm performance.     

碲铜系合金在饱和NH4Cl溶液中的腐蚀行为

用全浸失重法,研究了碲铜系合金在饱和NH4Cl溶液中的抗腐蚀性能,结合扫描电镜(SEM)、能谱仪(EDS)等测试方法,初步探讨了合金在饱和NH4Cl溶液中的腐蚀行为及腐蚀机制,结果表明碲铜系合金的抗腐蚀性优于纯铜,其腐蚀速率低于纯铜,原因在于碲、镁的加入,可降低纯铜中的非金属杂质含量,同时碲、镁的加入,可沿铜晶界以化合物的形式析出,有利地阻碍了纯铜的沿晶腐蚀.     

Hygroresponsive Torsional Yarns and Actuators Based on Cascade Amplification of the Deformation

Fiber-based hygroresponsive torsional actuators provide desirable merits, such as light weight and shapeability, for developing smart systems to harvest energy from moisture which is a ubiquitous natural resource. A key challenge in this development is to realize moisture-triggered actuation combining large actuation and rapid responses. Here, a multiscale design strategy is explored to create high-performance hygroresponsive torsional actuators consisting of chitosan and multiwalled carbon nanotubes (MWCNTs). The superior actuation performance arises from the synergism of contributing factors at different scales, including 1) MWNCTs accelerate the water transport in primary twisted fibers (PTFs), fostering the rotation of PTFs upon moisture stimuli; 2) in situ-formed hierarchically-assembled twists realize cascade amplification of moisture-triggered actuation. Specifically, PTFs are self-twisted to generate secondary helical yarns, that are subsequently over-twisted to yield tertiary coiled yarn. The resultant yarn actuator can reach a maximum rotation speed of 11 400 rpm in 5 s, output gravitational potential energy of 2.4 J kg⁻¹ and gravitational potential power of 0.053 W kg⁻¹ during contraction. This work represents the first design of fiber-based actuators by virtue of moisture-triggered in situ formation of yarns. The established principles of multiscale design will enable high-performance fiber-based hygroresponsive actuators toward advanced intelligent textile and soft robotics.     

多孔钯的制备及其结构与性能

研究了以钯粉和碳酸钠为原料制备多孔钯的烧结-溶解新工艺，用FESEM分析了多孔钯的微观结构形貌，并进一步研究了制备的多孔钯的力学性能和氢同位素的交排换代性能。结果表明，烧结-溶解工艺能稳定地制备出孔隙率为85．29％-87．82％的多孔钯，其压缩强度大于2MPa。室温下孔隙率为87.30％的多孔钯对氘的单位质量吸收量为0．0767L／g，氢同位素排代交换率为86．2％。     

延缓与加速A1-Cu合金时效析出反应的研究

研究了溶质原子浓度、Si晶体第二相、残余形变、外加莫来石(Mullite)短纤维及其交互作用，对二元Al—Cu合金时效析出行为的影响。试验材料采用挤压铸造方法制备，复合材料中纤维体积分数为18％。实验结果表明：随溶质原子浓度的升高，A1-Cu二元合金中GP，θ″和θ′相的析出都得到了相应加快；Si含量超过一定值后，随Si含量增加，A1-Cu-Si合金中GP区形成受到抑制，而θ″和θ′相的析出得到加快；形变对GP区的抑制和对θ″，θ′和θ相的加速析出具有十分明显的作用；纤维本身除对GP区抑制和对θ″，θ′相的析出加速外，还会与溶质原子、合金元素或第二相以及残余形变交互作用，使GP区被抑制，而θ″，θ′甚至θ相被加速析出等现象进一步加强。用位错理论能较好地解释析出反应延缓与加速的微观机理。