BaTiO_3纤维/PUIPN_s纳米复合体系导电性能研究

用红外光谱跟踪确定了同步互穿聚合物网络的形成工艺 ,并制成其梯次化复合涂层 ,TEM检测表明两相间的相畴尺寸在纳米级范围内 ;在此基础上 ,以钛酸钡超细纤维对此网络体系进行复合 ,确定偶联剂的加入量及复合工艺 ,测量了不同复合量下材料的电阻率 ,并考察了其伏安特性。此工作可为拓展此类材料的应用领域提供有价值的参考数据。     

An alternative to ratio method in sample surveys

Summary This paper examines a simple transformation which enables the use of product method in place of ratio method. The convenience with the former, proposed by Murthy [3], is that expressions for bias and mean square error (mse) can be exactly evaluated. The optimum situation in the minimum mse sense and allowable departures from this optimum are indicated. The procedure requires a good guess of a certain parameter, which does not seem very restrictive for practice. Two methods for dealing with the bias of the estimator are mentioned. An extension to use multiauxiliary information is outlined.     

Semi‐interpenetrating polymer networks composed of poly(N‐isopropyl acrylamide) and polyacrylamide hydrogels

Three series of semi‐interpenetrating polymer networks, based on crosslinked poly(N‐isopropyl acrylamide) (PNIPA) and 1 wt % nonionic or ionic (cationic and anionic) linear polyacrylamide (PAAm), were synthesized to improve the mechanical properties of PNIPA gels. The effect of the incorporation of linear polymers into responsive networks on the temperature‐induced transition, swelling behavior, and mechanical properties was studied. Polymer networks with four different crosslinking densities were prepared with various molar ratios (25:1 to 100:1) of the monomer (N‐isopropyl acrylamide) to the crosslinker (methylenebisacrylamide). The hydrogels were characterized by the determination of the equilibrium degree of swelling at 25 °C, the compression modulus, and the effective crosslinking density, as well as the ultimate hydrogel properties, such as the tensile strength and elongation at break. The introduction of cationic and anionic linear hydrophilic PAAm into PNIPA networks increased the rate of swelling, whereas the presence of nonionic PAAm diminished it. Transition temperatures were significantly affected by both the crosslinking density and the presence of linear PAAm in the hydrogel networks. Although anionic PAAm had the greatest influence on increasing the transition temperature, the presence of nonionic PAAm caused the highest dimensional change. Semi‐interpenetrating polymer networks reinforced with cationic and nonionic PAAm exhibited higher tensile strengths and elongations at break than PNIPA hydrogels, whereas the presence of anionic PAAm caused a reduction in the mechanical properties. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3987–3999, 2004     

Grafted interpenetrating polymeric systems based on cross-linked siloxaneurethanes

A series of cross-linked polysiloxaneurethanes with different functional groups in the nodal organosilicon fragment and related grafted interpenetrating polymeric systems with poly(methyl methacrylate) were synthesized, and their structural relaxation and mechanical properties were studied. Specific features of microphase separation and the mechanism of molecular mobility in these systems were considered.Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1946–1951, September, 2004.     

聚氨酯／聚（苯乙烯—甲基丙烯酸甲酯—甲基丙烯酸互穿聚合物网络的研究

研究了聚氨酯／聚互穿合笺网络，动态力学性能及透射电镜结果均表明该体系相分离较严重。ＩＮＰ具有两个玻璃化转变温度，它们有不同程度的内移，形成一定程度分子水平的混合。而ＩＰＮ（５０／５０）其分子混合水平较大，互穿缠结程度较高。     

Nanoscale Parallel Circuitry Based on Interpenetrating Conductive Assembly for Flexible and High‐Power Zinc Ion Battery

High‐rate capability has become an important feature for energy storage devices, but it is often accompanied with a significant reduction in energy density. Therefore, developing an energy storage technology that combines high‐rate capability with high energy density is a great challenge for next‐generation electronic devices. Here, parallel circuitry is constructed at the nanoscale to lower the resistance for ion and electron transport that largely determines the rate performance. The parallel circuitry is constructed through intertwining continuous carbon nanotubes with an interpenetrating conductive assembly based on hierarchically layered MXene (Ti₃C₂T_x ) functionalized by KMnO₄ (MnO_x @Ti₃C₂T_x ). The assembly shows ultrafast rate capability, e.g., maintaining 50% capacity when the current density increases from 0.1 to 10 A g^?1. Investigations of the kinetics and charge storage mechanisms confirm the efficiency of the designed parallel circuitry in improving rate capability by providing rapid pathways for ions and electrons, as well as dividing the current flow evenly into individual MnO_x @Ti₃C₂T_x flakes in the assembly. The flexible MnO_x @Ti₃C₂T_x based electrode endows zinc ion batteries with outstanding mechanical robustness and good power delivering performance. The paradigm presented here paves a new way for designing electrodes with high‐rate capability toward next‐generation energy storage technologies.     

Organic-inorganic gels based on silica and multifunctional acrylates

Rigid, microporous silica rods, prepared previously by the sol-gel process, were infiltrated with three triacrylate monomers to give sequential interpenetrating networks (IPNs). The three commercially available triacrylate monomers are glycerol propoxy triacrylate (GPTA), trimethylolpropane triacrylate (TMPTA) and pentaerythritol triacrylate (PETA). Each solution containing a photoinitiator was allowed to infiltrate the silica rod, after which the sample was UV irradiated to polymerize the triacrylate monomer. Emphasis was placed on establishing the infiltration and polymerization conditions leading to optically transparent composites. For comparison, one of the triacrylates (GPTA) was introduced into a hydrolyzing sol-gel formulation containing TEOS, ethanol, water and acid catalyst, to effect a simultaneous IPN. The sequential IPN and the simultaneous IPN samples gave similar transmission curves, despite differences in skeletal density.1992 Fulbright Visiting Scholar, on leave from Marie Curie Sklodowska University, Lublin, Poland.     

Swelling characterization of novel ternary semi‐IPNs: acrylamide/1‐vinylimidazole/PEG hydrogels

New ternary semi interpenetrating polymer networks (semi‐IPNs) systems containing acrylamide (AAm), 1‐vinylimidazole (VI) and poly (ethylene glycol) (PEG) have been prepared. AAm/VI hydrogels and semi‐IPN's, poly (AAm/VI/PEG) with 0.25, 0.50, 0.75 and 1.00 g of PEG (per 1.00 g AAm) were prepared by free radical solution polymerization in aqueous solution of AAm with VI as comonomer and a multifunctional crosslinker such as 1,4 butanediol dimethacrylate (BDMA). Swelling experiments were performed in water at 25°C, gravimetrically. The influence of VI and PEG content in hydrogels were examined. AAm/VI and AAm/VI/PEG hydrogels showed large extents of swelling in aqueous media, the swelling being highly dependent on the chemical composition of the hydrogels. Percentage swelling ratio of AAm/VI hydrogels and AAm/VI/PEG hydrogels was shown as 650–4167%. The values of equilibrium water content (EWC) of the hydrogels are between 0.8990 and 0.9750. Diffusion behavior was investigated. Water diffusion into hydrogels was found to be non‐Fickian in character. Copyright © 2007 John Wiley & Sons, Ltd.     

pH‐Modulating Poly(ethylene glycol)/Alginate Hydrogel Dressings for the Treatment of Chronic Wounds

The development of chronic wounds has been frequently associated with alkaline pH values. The application of pH‐modulating wound dressings can, therefore, be a promising treatment option to promote normal wound healing. This study reports on the development and characterization of acidic hydrogel dressings based on interpenetrating poly(ethylene glycol) diacrylate/acrylic acid/alginate networks. The incorporation of ionizable carboxylic acid groups results in high liquid uptake up to 500%. The combination of two separate polymer networks significantly improves the tensile and compressive stability. In a 2D cell migration assay, the application of hydrogels (0% to 1.5% acrylic acid) results in complete “wound” closure; hydrogels with 0.25% acrylic acid significantly increase the cell migration velocity to 19.8 ± 1.9 µm h⁻¹. The most promising formulation (hydrogels with 0.25% acrylic acid) is tested on 3D human skin constructs, increasing keratinocyte ingrowth into the wound by 164%.

     

聚丙烯酸酯－环氧树脂IPN乳液的合成

研究摩岩石刻保护材料聚丙烯酸酯-环氧树脂互穿聚合物网络乳液的合成,讨论影响凝聚率,乳液稳定性和乳液胶膜耐水性、吸水率的因素,得到最佳工艺条件。