胺化聚苯乙烯树脂的合成及其吸附性能

以氯甲基化聚苯乙烯树脂微球为母体,分别与三乙烯四胺和1,4,7,10-四氮杂环十二烷反应制备了胺化聚苯乙烯树脂(PS-TETA)和新型Cyclen型聚苯乙烯树脂(PS-Cy)。采用FTIR和BET方法表征了树脂的结构;利用紫外-可见分光光度计研究了树脂对对硝基苯酚(PNP)的吸附性能。表征结果显示,PS-TETA和PS-Cy可吸附PNP。实验结果表明,随PNP溶液p H的增大,PS-TETA和PS-Cy对PNP的吸附呈先增大后趋于平缓再不断下降的趋势,吸附过程符合准二级动力学方程,且主要控制步骤为Boyd液膜扩散形式。25℃下,PS-TETA和PS-Cy对PNP的平衡吸附量分别为126.34 mg/m L和118.93 mg/m L。PSTETA吸附PNP为多分子层吸附;PS-Cy对PNP的吸附为单分子层吸附。两者对PNP的吸附过程均为放热过程,且以物理吸附的形式为主。     

氮掺杂TiO_2中空复合微球的制备及可见光光催化性能

为了提高TiO2的可见光光催化性能,以微米级聚苯乙烯微球为模板,钛酸四丁酯为前驱体,三乙胺为氮源,采用静电吸附自组装法制备了粒径为1.20μm、壳层的厚度约为30nm且球形形貌良好的氮掺杂TiO2中空复合微球,采用SEM、XPS、XRD和紫外-可见分光光度计研究了其结构及光催化性能。结果表明:氮进入TiO2晶格内取代了部分O并改变了晶格中Ti和O的化学状态,但对TiO2晶型结构没有明显影响;氮掺杂后的TiO2中空复合微球禁带宽度变窄,氮掺杂TiO2中空复合微球不仅在紫外区有较强的光吸收能力,在可见光区也表现出较强的光响应性,对甲基橙的光催化降解率较Degussa P25型纳米TiO2的明显增强。研究结果对TiO2在光催化领域的应用具有理论指导意义。     

Morphology,structure, and photovoltaic properties of poly(3‐hexylthiophene) and [6,6]‐phenyl‐C61‐butyric acid methyl ester‐based ternary blends doping with polystyrene of different tacticities

The influence of the polystyrene of different tacticities on the morphology, phase structure, and photovoltaic properties of poly(3‐hexylthiophene) (P3HT) and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) blend has been extensively investigated. The atactic polystyrene (aPS) immiscible with P3HT tended to form the phase‐separated and columnar structure at low aPS weight ratio. Besides, the aPS could migrate to the surface of the films with PCBM phase distributing in the interfaces between P3HT and aPS domains at high aPS weight ratio of 75 wt %. The syndiotactic polystyrene (sPS) immiscible with P3HT could induce the crystallization of P3HT at low weight ratio of 3 wt %. The device based on aPS/P3HT/PCBM ternary blend showed of power conversion efficiency (PCE) of 1.2% even at aPS weight ratio of 50 wt %. However, the device based on sPS/P3HT/PCBM exhibited a sharp decrease in PCE value from 2.3% to 0.6% at sPS weight ratio of 3 wt %, due to the change in film morphology. The performance of the solar cell is believed to be determined by the morphology and phase structure of the ternary blends as revealed by the atomic force microscopy and UV‐vis spectra analysis. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41823.     

Pickering Emulsion Polymerization of Styrene using Nano-SiO2 and Subsequent Use of the Produced Core–Shell Structures as Fillers for Ethylene Vinyl Acetate Copolymer and Polypropylene

Solid particles can stabilize emulsions instead of conventional surfactants. Emulsion polymerization of styrene, as an example of polymerizable oil, was processed in the present work after ultrasonication of styrene in water in the presence of silica nanoparticles as stabilizer. Field emission scanning electron microscopy, equipped with energy-dispersive X-ray unit, and transmission electron microscopy confirmed the formation of polystyrene particles covered by a sheath of self-assembled silica. Addition of these hybrids in different loadings (2–14 wt%) to polypropylene and ethylene vinyl acetate copolymer could improve their tensile strength and hardness. The mechanical enrichment could be attributed to the action of the silica shell layer to delay the phase separation process encountered between the polystyrene from one side and polypropylene/ethylene vinyl acetate from other side, which translates into different extents of reinforcements.     

Polystyrene composites of single‐walled carbon nanotubes‐graft‐polystyrene

Single‐walled carbon nanotubes (SWCNTs) dispersed in N‐methylpyrrolidone (NMP) were functionalized by addition of polystyryl radicals from 2,2,6,6‐tetramethyl‐1‐piperidinyloxy‐ended polystyrene (SWCNT‐g‐PS). The amount of polystyrene grafted to the nanotubes was in the range 20‐25 wt% irrespective of polystyrene number‐average molecular weight ranging from 2270 to 49 500 g mol^?1. In Raman spectra the ratios of D‐band to G‐band intensity were similar for all of the polystyrene‐grafted samples and for the starting SWCNTs. Numerous near‐infrared electronic transitions of the SWCNTs were retained after polymer grafting. Transmission electron microscopy images showed bundles of SWCNT‐g‐PS of various diameters with some of the polystyrene clumped on the bundle surfaces. Composites of SWCNT‐g‐PS in a commercial‐grade polystyrene were prepared by precipitation of mixtures of the components from NMP into water, i.e. the coagulation method of preparation. Electrical conductivities of the composites were about 10^?15 S cm^?1 and showed no percolation threshold with increasing SWCNT content. The glass transition temperature (T_g) of the composites increased at low filler loadings and remained constant with further nanotube addition irrespective of the length and number of grafted polystyrene chains. The change of heat capacity (ΔC_p) at T_g decreased with increasing amount of SWCNT‐g‐PS of 2850 g mol^?1, but ΔC_p changed very little with the amount of SWCNT‐g‐PS of higher molecular weight. The expected monotonic decrease in ΔC_p coupled with the plateau behavior of T_g suggests there is a limit to the amount that T_g of the matrix polymer can increase with increasing amount of nanotube filler. Copyright © 2012 Society of Chemical Industry     

气相沉积CF改性PS的选择性激光烧结

由于普通碳纤维(CF)对聚苯乙烯(PS)烧结件弯曲强度的改善有限,在前期理论及实验基础上,对CF材料做气相沉积处理,制备PS/CF复合材料,再进行选择性激光烧结(SLS)实验,验证其增强效果;然后,改变经气相沉积法处理的CF与PS的配比,分析CF含量对制件强度及精度的影响;最后结合扫描电子显微镜(SEM)观察烧结件断面内部结构并进行分析。结果表明,经气相沉积处理的CF含量为10%时复合材料的弯曲强度较高,达10.17 MPa,比纯PS制件提高约76.3%。微观形貌SEM显示,随着CF含量的增加,孔隙量增加,从而导致SLS烧结件的强度降低。     

Synthesis of functionalized polymeric adsorbent selective to cobalt

Amino derivative of chloromethylated polystyrene resin was synthesized and functionalized by 1,10‐phenanthroline (1,10‐Phen) to yield a novel adsorbent, namely 4‐methylamino‐[N,N‐bis(2,2^′)‐1,10‐phenanthroline] polystyrene ( 4‐MABPPS ). The complete development of novel adsorbent along with its characterization is described in detail. The adsorption ability and selectivity of 4‐MABPPS were investigated for cobalt and zirconium ions so as to efficiently separate cobalt ion impurities from zircalloy cladding material of nuclear reactors. The experimental results showed selective uptake of cobalt by the adsorbent in the presence of zirconium. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

联合泡沫混凝土与EPS处理软基模拟研究

简要介绍并对比了泡沫混凝土与EPS材料的基本特性,为进一步减轻路堤对原路基的附加应力,提出联合应用泡沫混凝土与EPS材料处理软基的新方法,并借以规划中的中开高速所得勘察数据为依托,采用理论计算与Midas GTS NX数值模拟计算得出结果并对比分析。     

Study of the Formation of Nano-Networks in Colloidal Particles

The authors studied the formation of a wafer-scale network of connected colloidal beads by reactive ion etching. The dimensions of the connections have been studied as a function of etching time for colloidal beads of different sizes, and could be well controlled. The authors have found that the nano-network forms and disappears for the same time of etching independent of the diameter of the polystyrene beads. With recent interest of connected colloidal networks in various optical sensing applications, such as photonic crystals, as surface-enhanced Raman scattering substrates, the studies have potential uses in the development of wafer-scale nanophotonic sensors.