Formation of a large‐scale shish‐kebab structure of polyoxymethylene in the melt spinning and the crystalline morphology evolution after hot stretching

Polyoxymethylene (POM) fiber was produced by melt spinning with a high take‐up speed, which imposed a strong flow field. An unexpected formation of a shish‐kebab morphology with multiple shish of POM fibers was reported for the first time. This morphology is a large‐scale shish kebab with a diameter of 10.5 µm. Further orientation of the POM fiber was obtained by hot stretching twice at 160°C. Two crystalline morphology evolution processes were also observed: (i) the process from the large‐scale shish‐kebab to the deformed small shish‐kebab and (ii) the process from the deformed small shish‐kebab to the perfect whiskers. Compared with the melt spinning fiber, fiber tensile strength with first and second hot stretching increased by 976% and 1705%, respectively. The crystalline melting behavior of fibers significantly changes after the first and second hot stretching. The flow field induces a large number of extended chain crystals. Copyright © 2014 John Wiley & Sons, Ltd.     

Nano Carbon Doped Polyacrylamide Gel Electrolytes for High Performance Supercapacitors

Novel polyacrylamide gel electrolytes (PGEs) doped with nano carbons with enhanced electrochemical, thermal, and mechanical properties are presented. Carboxylated carbon nanotubes (fCNTs), graphene oxide sheets (GO), and the hybrid of fCNT/GO were embedded in the PGEs to serve as supercapacitor (SC) electrolytes. Thermal stability of the unmodified PGE increased with the addition of the nano carbons which led to lower capacitance degradation and longer cycling life of the SCs. The fCNT/GO-PGE showed the best thermal stability, which was 50% higher than original PGE. Viscoelastic properties of PGEs were also improved with the incorporation of GO and fCNT/GO. Oxygen-containing functional groups in GO and fCNT/GO hydrogen bonded with the polymer chains and improved the elasticity of PGEs. The fCNT-PGE demonstrated a slightly lower viscous strain uninform distribution of CNTs in the polymer matrix and the defects formed within. Furthermore, ion diffusion between GO layers was enhanced in fCNT/GO-PGE because fCNT decreased the aggregation of GO sheets and improved the ion channels, increasing the gel ionic conductivity from 41 to 132 mS cm⁻¹. Finally, MnO₂-based supercapacitors using PGE, fCNT-PGE, GO-PGE, and fCNT/GO-PGE electrolytes were fabricated with the electrode-specific capacitance measured to be 39.5, 65.5, 77.6, and 83.3 F·g⁻¹, respectively. This research demonstrates the effectiveness of nano carbons as dopants in polymer gel electrolytes for property enhancements.     

Synthesis of nanosized BaSO4 and CaCO3 particles with a membrane reactor: effects of additives on particles

Nanosized BaSO(4) particles, about 15 nm in size, were synthesized successfully by a membrane reactor at the aids of additives, in which Na(2)SO(4) solutions were added into BaCl(2) solutions gradually through the micropores of ultrafiltration membranes to control the saturation ratio, subsequently the nucleation and growth rates. The effects of additives species, additives concentrations, and membranes molecular weight cut-off (MWCO) on the particle morphology, along with the formation processes of particles, were investigated. CaCO(3) nanoparticles of 30-60 nm in size were also prepared by the reactor. The results revealed that the addition of methyl alcohol, ethanol etc. favor the synthesis of nanoparticles with small size. The particles size decreases with the increase in ethanol concentrations. With the increase in membrane MWCO, the products tend from nanoparticles towards aggregates.     

Propagation of instability in dielectric elastomers

When an electric voltage is applied across the thickness of a thin layer of an dielectric elastomer, the layer reduces its thickness and expands its area. This electrically induced deformation can be rapid and large, and is potentially useful as soft actuators in diverse technologies. Recent experimental and theoretical studies have shown that, when the voltage exceeds some critical value, the homogenous deformation of the layer becomes unstable, and the layer deforms into a mixture of thin and thick regions. Subsequently, as more electric charge is applied, the thin regions enlarge at the expense of the thick regions. On the basis of a recently formulated nonlinear field theory, this paper develops a meshfree method to simulate numerically this instability.     

关于4-苯基-2-丁酮与饱和亚硫酸氢钠加成反应的探讨

亚硫酸氢钠与醛酮的加成是比较经典的反应 ,但在与 4 苯基 2 丁酮的反应中 ,传统的实验反应条件并不一定是最佳选择     

关于功的一种新的教学思路*--从概念起源和科学方法的角度学习

针对“功”的教学现状,在查阅资料中,我们认为不仅可以引导学生从概念起源的角度来学习功,更可以让学生在学习功的概念之中体会和感悟物科学方法。我们提出全新的教学设计,并在教学实践之中进行尝试。在这样的教学设计和实践中,学生们明确功的概念起源之后,在头脑中自然形成判断一个力是否做功的逻辑依据,并且按照逻辑顺序自然掌握了计算一个力做功多少的方法。     

High‐Performance Quinoline‐Malononitrile Core as a Building Block for the Diversity‐Oriented Synthesis of AIEgens

In vivo fluorescent monitoring of physiological processes with high‐fidelity is essential in disease diagnosis and biological research, but faces extreme challenges due to aggregation‐caused quenching (ACQ) and short‐wavelength fluorescence. The development of high‐performance and long‐wavelength aggregation‐induced emission (AIE) fluorophores is in high demand for precise optical bioimaging. The chromophore quinoline‐malononitrile (QM) has recently emerged as a new class of AIE building block that possesses several notable features, such as red to near‐infrared (NIR) emission, high brightness, marked photostability, and good biocompatibility. In this minireview, we summarize some recent advances of our established AIE building block of QM, focusing on the AIE mechanism, regulation of emission wavelength and morphology, the facile scale‐up and fast preparation for AIE nanoparticles, as well as potential biomedical imaging applications.     

Fabrication and properties of thermosensitive organic/inorganic hybrid hydrogel thin films

We report on a facile method for fabricating thermosensitive organic/inorganic hybrid hydrogel thin films from a cross-linkable organic/inorganic hydrid copolymer, poly[ N-isopropylacrylamide- co-3-(trimethoxysilyl)propylmethacrylate] [P(NIPAm- co-TMSPMA)]. Fourier transform infrared (FT-IR) spectra confirmed the formation of hybrid hydrogel thin films after hydrolysis of the methoxysilyl groups (Si-O-CH 3) and subsequent condensation of the silanol groups (Si-OH). Atomic force microscopy (AFM) images revealed that the surface morphology of the hydrogel thin films depended on the supporting substrates. Microdomains were observed for the hydrogel thin films on a gold surface, which can be attributed to inhomogeneous network structures. The thermoresponsive swelling-deswelling behavior and the viscoelastic properties of the hydrogel thin films were investigated as a function of temperature (25-45 degrees C) by using a quartz crystal microbalance (QCM) operated in water. The high frequency shear modulus of the P(NIPAm- co-TMPSMA) hydrogel thin films was several hundred kilopascals.