Highly oriented and ordered microstructures in block copolymer films

Block copolymer (BCP) films with long-range lateral ordering and orientation are crucial for many applications. Here, we report a simple, versatile strategy based on a solution casting procedure, to produce millimeter thick film of BCPs with highly oriented nanostructures. Transmission electron microscope (TEM), small angle X-ray scattering (SAXS), and Hansen solubility parameters were used to study the morphology and interactions of the system. A variety of BCP-solvent pairs were investigated. Factors including set-up geometry, BCP characteristics, solvent evaporation, surface tension, and interactions, such as solvent-BCP, solvent-substrate, and BCP-substrate were examined. A mechanism is proposed to describe the observed long-range lateral ordering and orientation in films up to 1 mm in thickness. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 1369–1375     

Design of a small-sized expanded coaxial line antenna at L-band

为了减小常规L波段高功率微波测量接收天线的结构尺寸及增益,设计了一种基于轴向缝隙馈电的小型化同轴扩张型天线.通过理论分析和数值模拟,选择了较优的结构尺寸,得到天线的增益及方向图特性:在1.3～1.6 GHz范围内,增益从-2.0 dBi变化至0.8 dBi；天线最大辐射方向在物理结构轴向.基于矢量网络分析仪E8362B的天线特性测量结果与数值计算结果基本一致:工作频率从1 3～1 6GHz变化时,增益从-2.3 dBi变化至1.2 dBi；E面方向图主瓣宽度大于 60°,轴向轴比大于35dB,结果表明设计的天线能够满足L波段高功率微波渊量天线低增益小型化要求.     

Synthesis of ethylene/vinyl ester copolymers with pendent linear branches via ring‐opening metathesis polymerization of fatty acid‐derived cyclooctenes

Fatty acid‐derived cyclooctenes, including n‐hexanoic acid ( M1 ), n‐octanoic acid ( M2 ), lauric acid ( M3 ), and palmitic acid ( M4 ), were prepared as monomers and polymerized by ring‐opening metathesis polymerization (ROMP) using Grubbs second‐generation catalyst ( G2 ). In all the cases, the regio‐irregular unsaturated polymers with pendent linear branches were obtained, which could be saturated by chemical hydrogenation with TSH/TPA in high conversion, yielding ethylene/vinyl ester copolymers with pendent linear branches on precisely every eighth backbone carbon. Both unsaturated and saturated polymers were amorphous, and their structures were characterized by FTIR, ¹H and ¹³C NMR spectra, and elemental analysis. Differential scanning calorimetry (DSC) and thermo‐gravimetric analysis (TGA) were used to study their thermal properties. The chain length of branches greatly affected the thermal properties of polymers. After hydrogenation, the thermal degradation stability of polymers was relatively improved. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2211–2220     

A stable solid acid material: Sulfated ZrO2 dispersed on alumina nanotubes

Russian Journal of Physical Chemistry A - A tubular solid acid catalyst was designed by loading sulfated zirconia into γ-Al2O3 nanotubes using the method of stepwise deposition. The XRD, N2...     

Synthesis and proton conductivity of sulfonated,multi‐phenylated poly(arylene ether)s

A series of sterically‐encumbered, sulfonated, poly(arylene ether) copolymers were synthesized and their proton conductivity examined. The series was prepared by copolymerizing a novel monomer, 2″,3″,5″,6″‐tetraphenyl‐[1,1′:4',1″:4″,1″':4″',1″″‐quinquephenyl]‐4,4″″‐diol, with 4,4'‐difluorobenzophenone and bisphenol A. Subsequent sulfonation and solution casting provided membranes possessing ion exchange capacities of 1.9 to 2.7 mmol/g and excellent mechanical properties (Young's modulus, 0.2–1.2 GPa; tensile strength, 35–70 MPa; elongation at break, 62–231%). Water uptake ranged from 34 to 98 wt% at 80 °C/100% RH. Proton conductivities ranged between 0.24 to 16 mS/cm at 80 °C/60% RH, and 3 to 167 mS/cm at 80 °C/95% RH. TEM analysis of the polymers, in the dehydrated state, revealed isolated spherical aggregates of ions, which presumably coalesce when hydrated to provide highly conductive pathways. The strategy of using highly‐encumbered polymer frameworks for the design of mechanically‐robust and dimensionally‐stable proton conducting membranes is demonstrated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2579‐2587     

化学教育研究:范式的转变

化学教育起源于化学科学,是科学教育的一个重要分支。在回顾中外化学教育研究不同发展路径的基础上,提出我国化学教育学科要努力从“教学法”范式转变为实证研究范式。探讨了基于证据的化学教育研究的3个主要议题,即研究问题、理论基础和研究方法,介绍了基于证据的化学教育研究的论文写作规范。最后对在我国化学教育界推进实证研究提出若干建议。     

A group adaptive elastic-net approach for variable selection in high-dimensional linear regression

In practice, predictors possess grouping structures spontaneously. Incorporation of such useful information can improve statistical modeling and inference. In addition, the high-dimensionality often leads to the collinearity problem. The elastic net is an ideal method which is inclined to reflect a grouping effect. In this paper, we consider the problem of group selection and estimation in the sparse linear regression model in which predictors can be grouped. We investigate a group adaptive elastic-net and derive oracle inequalities and model consistency for the cases where group number is larger than the sample size. Oracle property is addressed for the case of the fixed group number. We revise the locally approximated coordinate descent algorithm to make our computation. Simulation and real data studies indicate that the group adaptive elastic-net is an alternative and competitive method for model selection of high-dimensional problems for the cases of group number being larger than the sample size.     

Preparation of BiVO4/MIL‐125(Ti) composite with enhanced visible‐light photocatalytic activity for dye degradation

Because of their desired features, including very specific surface areas and designable framework architecture together with their possibility to be functionalized, Metal Framework (MOF) is a promising platform for supporting varied materials in respect of catalytic applications in water treatment. In this work, a novel visible‐light‐responsive photocatalyst that comprised BiVO₄ together with MIL‐125(Ti), was synthesized by a two‐step hydrothermal approach. The characterization of as‐obtained samples as performed by X‐ray diffraction, scanning electron microscopy, high resolution transmission electron microscopy, Fourier transform infrared spectroscope, X‐ray photoelectron spectroscopy and ultraviolet‐visible diffuse reflection spectra. Rhodamine B was selected being a target for the evaluation of the photocatalytic function of as‐developed photocatalyst. The photocatalytic reaction parameters, for example, the content of BiVO₄ as well as initial concentration of Rhodamine B was researched. The composite photocatalyst possessing Bi:Ti molar ratio of 3:2 brought to light the fact that the greatest photocatalytic activity had the ability to degrade 92% of Rhodamine B in 180 min. In addition to that, the BiVO₄/MIL‐125(Ti) composite could keep its photocatalytic activity during the recycling test. The phenomenon of disintegration of the photo‐generated charges in the BiVO₄/MIL‐125(Ti) composite was brought to discussion as well.