Synthesis of azo chromophores by using a polymer‐supported sodium nitrite

Polymer supported reagents especially anion exchange resins have been widely applied in organic synthesis. The recent developments in polymer‐supported reactions have led to the propagation of combinatorial chemistry as a method for the rapid and efficient preparation of novel functionalized molecules. An interesting and fast growing branch of this area is polymer‐supported reagents. In this study, diazonium salts are generated and are coupled with a coupling component by using a polymer supported nitrite and a polymeric acid. In this procedure, the azo chromophores are formed in a clean and efficient manner, the work‐up is easy and yields are high to excellent. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Regioselective and green synthesis of nitro aromatic compounds using polymer‐supported sodium nitrite/KHSO4

Polymer supported reagents have become the subject of considerable and increasing interest as insoluble materials in the organic synthesis. Use of polymeric reagents simplifies routine nitration of aromatic compounds because it eliminates traditional purification. In this article, the use of readily available cross‐linked poly(4‐vinylpyridine) supported sodium nitrite, [P₄‐Me] NO₂, as an efficient polymeric nitrating agent in the presence of KHSO₄ is described. A good range of available aromatic compounds were also subjected to nitration in the presence of [P₄‐Me] NO₂/KHSO₄. This reagent is regioselective and chemoselective nitrating polymeric reagent for activated aromatic rings. In this procedure, the work‐up is easy, and the spent polymeric reagent is easily regenerated and reused. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Development of biodegradable scaffold using polylactic acid and polycaprolactone for cardiovascular application

The limitations of newly synthesized biodegradable stents are low mechanical strength, fracture stiffness, and fast degradability of the polymers. A cylindrical polymeric scaffold was proposed in combination of polylactic acid and polycaprolactone. The tensile strength of the blend was increased twice, though elongation has reduced threefold. The blend illustrated no chemical interaction between polymers. The scaffold was coated with docetaxel, and sustained release profile was observed for 56 days. The degradation of the scaffold was evaluated through change in mechanical properties, weight variation, and morphological studies. The developed hemocompatible polymeric scaffold may be used as for the cardiovascular application.     

Block copolymers as polymeric stabilizers in non‐aqueous emulsion polymerization

This review summarizes the background and recent advances of block copolymer stabilized oil‐in‐oil emulsions. For non‐polymerizable emulsions which have promising application possibilities for biomedical and cosmetic formulations, it is shown that tailor‐made block copolymers are by far the most efficient stabilizers with respect to low molecular weight surfactants. The characteristic features of oil‐in‐oil emulsions comprising one polymerizable phase are described. These types of non‐aqueous emulsions are of interest as nanoreactor systems for the polymerization of moisture‐sensitive monomers or catalysts. Furthermore they are the starting point of novel heterophase polymerization processes for the preparation of sterically stabilized polymer particles, as well as of ‘liquid‐filled polymeric materials’. The concept of oil‐in‐oil emulsions is finally extended to those systems where the two phases are polymerizable by distinct polymerization mechanisms. This approach could offer attractive possibilities for the development of special coatings with neither water nor solvent evaporation in their drying or curing step. Copyright © 2011 Society of Chemical Industry     

pH响应型星状聚合物胶束的制备及释药性能

以金刚烷为核设计合成了一种具有pH响应功能的四臂星状聚合物金刚烷-[聚(乳酸-共-羟基乙酸)-聚甲基丙烯酸二乙氨基乙酯-聚(乙二醇)单甲醚]4(4sAd-PLGA-D-P),制备了4sAd-PLGA-D-P自组装胶束,考察了该胶束对抗癌药物阿霉素(Doxorubicin,DOX)的控释性能.结果表明:改变聚甲基丙烯酸二...     

煤矸石制备聚合氯化铝铁钙与应用试验研究

以煤矸石为原料,经过高温焙烧、酸浸、聚合、熟化等过程制备了高效无机高分子絮凝剂聚合氯化铝铁钙（PAFCC）,通过单因素试验研究了PAFCC制备条件对浊度、COD和UV₂₅₄去除率的影响。试验结果表明,PAFCC最佳聚合条件为pH值2、聚合温度60℃、聚合时间5 h、在40℃下熟化28 h。混凝结果表明：制备的PAFCC对浊度有极好的去除效果,达95.70%,同时,对COD、UV₂₅₄也有一定的去除效果,去除率分别达到47.51%、45.98%。炼化废水混凝结果表明：PAFCC对浊度和总磷有较好的去除效果,同时,对COD及氨氮也有一定的去除效果,效果明显优于传统PAC。     

n阶方阵求逆的两个公式

针对ｎ阶方阵的逆阵问题，分别利用矩阵乘积及正交化方法给出了求Ａ＾－１的两个表达式，从而达到运算量小且实用之目的。     

滚齿加工齿轮误差的矢量法分析

从共轭原理角度出发，采用矢量法分析了运动偏心下滚齿加工轮齿的本质，阐明了有运动偏心的情况下，滚切出的齿形是有误差的渐开线齿形。     

Terpolymers as precursors for CuO nanoparticles synthesis

This work describes the synthesis of terpolymers of aniline, diphenylamine, and o‐anthranilic acid (PANIDPAA) by 1 : 1 : 1 molar ratio of the respective monomers doped by different concentration of copper ions via in situ chemical terpolymerization. The results are justified by measuring spectral characteristics namely, UV‐vis absorption spectra, FTIR, and TGA. Calcining these PANIDPAA terpolymers doped by copper at temperatures in the range of 700°C led to the formation of CuO nanoparticles in the nanoscale by thermal decomposition in air directly. The stages of decompositions and the calcination temperature of the precursors have been determined from thermal analysis data sheet. The obtained CuO nanoparticles have been characterized by X‐ray diffraction and transmission electron microscope (TEM). TEM showed a particle size less than 40 nm. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41150.     

Synthesis,characterization and dielectric properties of nickel-based polyoxometalate/polyurethane composites

The aim of this study was to synthesis, characterization and investigation of the influence of the polyoxometalate concentrations (1, 3, 5 and 10 wt%) on chemical, thermal, physical and morphological properties of nickel-based polyoxometalate/polyurethane composite (Ni-POM/PU) materials. Firstly, nickel-based polyoxometalate (Ni-POM) compound has been synthesized and characterized through various spectroscopic techniques. Synthesized Ni-POM compounds have been used for preparation of polyurethane composites as a reinforcement. Three different Ni-POM/PU composites containing Ni-POM were prepared by solution mixing and casting techniques. The chemical structure and morphology of prepared Ni-POM/PU composite samples were confirmed by Fourier transform infrared spectroscopy (FTIR), elemental analysis and SEM techniques. Effects of Ni-POM on thermal stability, glass transition temperature, optical transparency, hydrophilicity and physical properties of polyurethane composites were examined. Thermal stabilities and glass temperatures of the materials have been checked by differential thermal analysis (DTA), thermogravimetric analysis (TGA) and differential scanning calorimeter (DSC). The SEM results confirmed the highly porous structure and the formation of Ni-POM structures in the polymer matrix. Synthesized composites showed high chemical stability, good processability, and low Tg values. The dielectric properties of the prepared Ni-POM/polyurethane composites were also investigated at room temperature. These results displayed that the dielectric constant of the POM/polyurethane composites decreased with the increase of the Ni-POM content in polymeric matrix.