Synthesis of propylene carbonate from carbon dioxide using trans‐dichlorotetrapyridineru‐ thenium(II) as catalyst

trans‐Dichlorotetrapyridineruthenium(II) [trans‐RuCl₂(py)₄] was synthesized and the structure was determined by single crystal X‐ray crystallography. Highly efficient formation of propylene carbonate (PC) from carbon dioxide and propylene oxide was achieved by using a catalyst system composed of trans‐RuCl₂(py)₄ and hexadecyl trimethyl ammonium bromide under mild conditions (4h, 80 °C, 3.0 MPa). PC was obtained in nearly 100% selectivity without the formation of a polymer. The catalyst could be recycled constantly many times without any significant loss of its catalytic activity. On the basis of the results, a mechanism for the reaction was proposed. Copyright © 2010 European Peptide Society and John Wiley & Sons, Ltd.     

A facile method for the preparation of monodisperse hollow silica spheres with controlled shell thickness

This article presents a facile, effective, mild synthesis process for well‐defined hollow spheres by using cationic polystyrene (PS) submicro‐particles as templates. In this approach, the cationic PS templates can be first prepared via emulsifier‐free polymerization by using the cationic monomer 2‐(methacryloyloxy) ethyltrimethylammonium chloride as comonomer, then, the silica shells from the sol‐gel process of tetraethoxysilane were coated on the surfaces of template particles via electrostatic interaction, finally the PS was dissolved in situ by modification of the reaction conditions in the same medium to form monodisperse hollow silica spheres with controlled shell thickness. Fourier transform‐infrared spectroscopy, thermogravimetric analysis, Brunauer‐Emmett‐Teller, transmission electron microscopy, and scanning electron microscope measurements were used to characterize these hollow silica spheres. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1332–1338, 2010     

Novel Method for Preparing NH4NiPO4·6H2O: Hydrogen Bonding Coacervate Selective Self-assembly

The single phase NH₄NiPO₄·6H₂O was synthesized by solid‐state reaction at room temperature using NiSO₄·6H₂O and (NH₄)₃PO₄·3H₂O as raw materials. The NH₄NiPO₄·6H₂O and its calcined products were characterized using X‐ray powder diffraction (XRD), thermogravimetry and differential thermal analyses (TG/DTA), Fourier transform IR (FT‐IR), ultraviolet‐visible (UV‐vis) absorption spectroscopy, and scanning electron microscopy (SEM). The results showed that the product dried at 80°C for 3 h was orthorhombic NH₄NiPO₄·6H₂O [space group Pmm2(25)], and surfactant polyethylene glycol (PEG)‐400 can direct growth of crystal NH₄NiPO₄·6H₂O. The thermal process of NH₄NiPO₄·6H₂O experienced three steps, which involve the dehydration of the five crystal water molecules at first, and then deamination, dehydration of the one crystal water, intramolecular dehydration of the protonated phosphate groups together, at last crystallization of Ni₂P₂O₇. The product of thermal decomposition at 150°C for 2 h, orthorhombic NH₄NiPO₄·H₂O, is layered compound with an interlayer distance of 0.8370 nm.     

中等组分网状结构局部微变对功能梯度板三维动力特性的影响

利用细观元方法根据材料实际金相图片信息进行材料参数输入,对发生局部网格变化的功能梯度板件进行三维动力特性分析,完成了材料细观结构与构件宏观响应间的跨尺度分析.细观元法在结构的常规有限元内部设置密集的细观单元来反映材料细观构造,此方法可实现材料细观结构到构件宏观响应的直接过渡分析,为具有细观结构微观变化的功能梯度板件的分析提供一种新的工具.利用细观元法对具有中等组分网状结构发生局部微变的功能梯度板进行三维动力特性分析,给出其固有频率及振型的三维分布,特别是功能梯度板应力振型的平面等值线图差异,得到较好的结果.     

Erratum to "Aerosol pollution in China: Present and future impact on environment"

PARTICUOLOGY regrets that the above paper was mistakenly classified as a ‘Review’ rather than an ‘Invited paper’ when originally published in volume 7, issue 6, 426–431.     

Study on Phase Equilibrium Properties for CO_(2+) Cosolvent Binary Systems

Recently, the application of supercritical fluid technology is very interested, and it is applied in many areas for its special properties. The performance of supercritical fluid (SCF) as a solvent can be greatly affected by addition of an entrainer to the system. An entrainer can be added to a supercritical fluid to enhance its solvent strength and/or selectivity. Critical point data for these dilute supercritical fluid-cosolvent systems are imperative for the design of efficient separation …     

Salt effects in capillary zone electrophoresis. IV. Resolution versus time and the effect of potassium phosphate and its concentration in the high ionic strength separation of sulphonamides.

The effects of potassium phosphate buffer and its concentration upon the capillary zone electrophoretic separation of 23 sulphonamides and a neutral marker were examined at pH 7. The resolution between the pairs was improved with the increased concentration of the buffer from 65 mM to 174 mM. Nineteen sulphonamides, a hydrolysis product and several unidentified minor components were baseline resolved in both 101 and 138 mM phosphate buffers. In 174 mM buffer all 21 ionised sulphonamides and the other compounds were separated. A simple relationship between the resolution of analyte pairs (Rs) and the square root of the mean analysis time for the pair (square root of tapp) was derived, but few of the pairs displayed this behaviour. For the majority of pairs of compounds, Joule heating appeared to cause a maximum in the Rs versus square root of tapp relationship, while non-ideality and shifts in ionisation with increasing salt concentration appeared dominant in other cases.     

推广的Volterra方程的极限环问题

在生物数学中,基本研究对象之一是系统 其中,b>0,c>0,d>0,a(x)为x的至少二阶可微函数。 系统(1)是描述捕食者——食饵相互作用的一种近似数学模型,是对Lotka—Volterra数学模型的推广。这里,x是指食饵种群的密度,y是指捕食者种群的密度,函数a(x)则描述了食饵种群在脱离捕食者情况下的增殖过程。     

Covalently attached self‐assembly of ultrathin films from hydroxy‐containing porphyrin and diazoresin

Ultrathin films from 5,10,15,20‐tetrakis(4‐hydroxyphenyl) porphyrin (HPP) and diazoresin (DR) via a H bonding interaction were fabricated with the self‐assembly technique. Under UV irradiation, the H bonds between the layers will convert to covalent bonds following the decomposition of the diazonium group of DR. The stability of the film against the polar solvent and electrolyte aqueous solution increases a lot because of the formation of the covalent crosslinking structure. Thus, the photoelectric conversion property of DR/HPP film can be measured directly with a normal photoelectric chemical cell with potassium chloride as the electrolyte. The maximum of the anodic photocurrent was measured as 1.7 μ Å for an eight bilayer DR/HPP film deposited on an indium–tin oxide glass electrode. The action spectrum of the photocurrent generation indicated that the HPP contained in the film is responsible for the generation of the observed photocurrent. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3103–3108, 2003