Factors affecting the mechanical properties of mica-filled polypropylenes

Water-ground Phlogopite mica (Kemira Siilinjarvi phlogopite) has been evaluated as a reinforcing filler in polypropylene. The major factors which influence the composite strength and modulus include the size, aspect ratio, and uniformity of the mica flakes. Aqueous delamination permits the production of very small flakes (less than 44 microns diameter) with aspect ratios near 50. Such small flakes impart greater tensile and modulus values to polypropylene than larger flakes and the former can also be reprocessed many times without any deterioration of properties. Surface treatment is necessary for adequate dispersion and coupling, particularly with the finely divided mica fillers. Other properties such as the heat-distortion temperature, fracture toughness, and gas permeability are also influenced by the mean size and aspect ratio of the mica filler. Guidelines are presented to indicate the preferred characteristics of mica fillers for optimum performance.     

C,CO and CO2 hydrogenation on cobalt foil model catalysts: evidence for the need of CoO reduction

The hydrogenation of C, CO, and CO₂ has been studied on polycrystalline cobalt foils using a combination of UHV studies and atmospheric pressure reactions in temperature range from 475 to 575 K at 101 kPa total pressure. The reactions produce mainly methane but with selectivities of 98, 80, and 99 wt% at 525 K for C, CO, and CO₂, respectively. In the C and CO₂ hydrogenation the rest is ethane, whereas in CO hydrogenation hydrocarbons up to C₄ were detected. The activation energies of methane formation are 57, 86, and 158 kJ/mol from C, CO, and CO₂, respectively. The partial pressure dependencies of the CO and CO₂ hydrogenation indicate roughly first order dependence on hydrogen pressure (1.5 and 0.9), negative first order on CO (–0.75) and zero order on CO₂ (–0.05). Post reaction spectroscopy revealed carbon deposition from CO and oxygen deposition from CO₂ on the surface above 540 K. The reduction of cobalt oxide formed after dissociation of C-O bonds on the surface is proposed to be the rate limiting step in CO and CO₂ hydrogenation.     

Blends of natural rubber and polyurethane latices studied by 1H wideline and 13C MAS solid‐state NMR

¹H wideline and ¹³C magic‐angle spinning NMR have been used to study the morphology and dynamics of latex‐cast and solution‐cast film blends of natural rubber (NR) and a polyurethane (PU) based on poly(?‐caprolactone) diol and isophorone di‐isocyanate. ¹H T₁ and T_1ρ relaxation times have been measured, and the extent of interpenetration of the NR and PU constituents has been monitored using the Goldman–Shen technique. The NMR spectra and relaxation properties indicated that the NR and PI constituents largely occupy separated domains on a distance scale of >10 nm. The Goldman–Shen experiments indicated that there was slightly greater contact between NR and PU in the solution‐cast samples than in the latex‐cast. The tensile properties of the films have been measured. The tensile strength and initial Young's modulus pass through a maximum at a PU content of about 50 wt%. © 2002 Society of Chemical Industry     

热泵干燥技术简介

简介热泵干燥技术原理，并通过热泵干燥超细粉末的实验与部分其他应用实例，说明该技术的节能特点及其应用前景。     

基于Matlab的RLC二阶电路零输入响应的研究

应用Matalb软件对RLC串联放电二阶电路的零输入响应进行了深入分析，给出了在3种情况下脉冲放电电流峰值im与R、L、C等参数的函数关系，用计算和绘图方法证明了在两种情况下不同形式的im=f(R、L、C）及i=f(t)、uc=f(t）等函数式的一致性，介绍了用能量平衡求该电路im值的方法。     

Fabrication and Characterization of Large Free-Standing Polarizer Grids for Millimeter Waves

Construction of large aperture free-standing metal wire grids is demonstrated for the lower end of the millimeter wave spectral region. For the constructed two grids the co-polarized and cross-polarized components of transmitted power were measured at 45° oblique incidence. The measurements were performed as a function of wire orientation angle and in more detail at selected angles. The results are in good agreement with the theoretical results presented in the literature. In order to save time and costs the construction apparatus was simplified from those reported previously by other authors. It was shown that for this frequency range the grid characteristics are not degraded when such an apparatus is applied. One of the constructed grids will be used in a calibration system of the Helsinki University of Technology (HUT) polarimetric radiometer.     

Preparation of hydrophobic poly(isobutylene) star polymers with hydrophilic poly(propylene imine) dendritic cores

Summary Poly(propylene imine) dendrimers with amino chain ends have been used for the preparation of hydrophobic star polymers with hydrophilic dendritic cores. The unsaturated end groups of polyisobutylene (PIB) were transformed into reactive anhydride end groups by an “ene” reaction with maleic anhydride, and the resulting functionalized PIB was then reacted with dendrimers to afford dendrimer-PIB star copolymers. Received: 20 May 1999/Accepted: 17 June 1999     

Molded rigid polymer monoliths as separation media for capillary electrochromatography. 2. Effect of chromatographic conditions on the separation

Monolithic columns for capillary electrochromatography have been prepared within the confines of untreated fused-silica capillaries in a single step by a simple copolymerization of mixtures of butyl methacrylate, ethylene dimethacrylate, and 2-acrylamido-2-methyl-1-propane-sulfonic acid (AMPS) in the presence of a porogenic solvent. The use of these novel macroporous monoliths eliminates the need for frits, the difficulties encountered with packed capillaries, and capillary surface functionalization. Since the porous properties of the monolithic materials can be easily tailored through changes in the composition of the ternary porogenic solvent, the effects of both pore size and the percentage of sulfonic acid monomer on the efficiency and the electroosmotic flow velocity of the capillary columns could be studied independently over a broad range. A simple increase in the content of charged functionalities within the monolith leads to an expected acceleration of the flow velocity. However, increasing the pore size leads to a substantial deterioration of the efficiency of the separation. In contrast, monoliths with increasing levels of AMPS in which the pore size remains fixed due to adjustments in the composition of the porogenic solvent show no deterioration in efficiency while maintaining the same increase in flow velocity, thus producing a significant reduction in separation time. Additionally, measurements on monoliths with constant levels of AMPS but different pore sizes suggest that flow velocity may be affected by the flow resistance within the capillary column.     

Monodisperse hydrolyzed poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads as a stationary phase for normal-phase HPLC

The basic characteristics of a rugged, stable, and highly efficient polymeric stationary phase for normal-phase HPLC prepared by hydrolysis of porous monodisperse poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads have been studied and compared with those of bare Nucleosil silica and Nucleosil silica-diol. As a result of their overall chemical composition and the more than 10-fold larger surface coverage with hydroxyl groups, the polymer beads provide much higher retention of model solute molecules. In contrast to silica hydroxyls, all of the polymer surface diol groups are chemically equal and homogeneously distributed over all of the surface. In addition, they are less acidic than typical silanol functionalities. The exceptional selectivity of the polymeric column can be controlled by the composition of the mobile phase, as demonstrated with a broad spectrum of separations involving positional isomers of benzene derivatives, nonpolar isobutylene copolymers with minute composition differences, and hydrophilic poly(ethylene oxides) differing only in their chain length. Unlike silica phases, the properties of the polymeric stationary phrase are not affected by the presence of water in the mobile phase. As a result, repetitive gradient separations in eluents ranging in polarity from hexane through tetrahydrofuran to water can be easily accomplished.     

Photoluminescence decay rate of silicon nanoparticles modified with gold nanoislands

We investigated plasmon-assisted enhancement of emission from silicon nanoparticles (ncs-Si) embedded into porous SiO _x matrix in the 500- to 820-nm wavelength range. In the presence in the near-surface region of gold nanoisland film, ncs-Si exhibited up to twofold luminescence enhancement at emission frequencies that correspond to the plasmon resonance frequency of Au nanoparticles. Enhancement of the photoluminescence (PL) intensity was attributed to coupling with the localized surface plasmons (LSPs) excited in Au nanoparticles and to increase in the radiative decay rate of ncs-Si. It has been shown that spontaneous emission decay rate of ncs-Si modified by thin Au film over the wide emission spectral range was accelerated. The emission decay rate distribution was determined by fitting the experimental decay curves to the stretched exponential model. The observed increase of the PL decay rate distribution width for the Au-coated nc-Si-SiO _x sample in comparison with the uncoated one was explained by fluctuations in the surface-plasmon excitation rate.

PACS

78. 67. Bf; 78.55.-m