Plasma graft polymerization of acrylamide onto crosslinked HTPB based PU membrane for pervaporation

Pervaporation of water-ethanol mixtures through plasma graft polymerization of acrylamide onto crosslinked hydroxyl terminated poly-butadiene (HTPB) based PU membranes, plasma graft polymerization of acrylamide onto crosslinked PU membrane (AAm-p-CPU), were investigated. The grafting was dependent on the discharge power and pretreatment period. The effects of crosslinking, plasma treatment conditions, feed compositions, and feed temperature on the performance of these membranes were studied. The physical properties of crosslinked membrane were better than those of the uncrosslinked membrane. In addition, compared with crosslinked PU membranes (CPU), the plasma modified crosslinked PU membranes effectively improve the pervaporation separation performances.     

Catalytic removal of SO2, NO and HCl from incineration flue gas over activated carbon-supported metal oxides

Activated carbon-supported copper, iron, or vanadium oxide catalysts were exposed to incineration flue gas to investigate the simultaneous catalytic oxidation of sulfur dioxide/hydrogen chloride and selective catalytic reduction of nitrogen oxide by carbon monoxide. The results show that AC-supported catalysts exhibit higher activities for SO₂ and HCl oxidation than traditional γ-Al₂O₃-supported catalysts and the iron and vanadium catalysts act as catalysts instead of sorbents, and can decompose sulfate with evolution of SO₃ and then regenerate for more SO₂ adsorption to take place. The AC-supported catalysts also display a high activity for NO reduction with CO generated from a flue gas incineration process and the presence of SO₂ in the incineration flue gas can significantly promote catalytic activity. Using CO as the reducing agent for NO reduction is more effective than using NH₃, because NH₃ may be partially oxidized in the presence of excess O₂ (12 vol%. in the incineration flue gas used) to form N₂, which can decrease the overall extent of NO reduction.     

Miscibility, crystallization and morphologies of syndiotactic polystyrene blends with isotactic polystyrene and with atactic polystyrene

Two-component blends of differing polystyrene (PS), one syndiotactic (sPS) and the other isotactic (iPS) or atactic (aPS), were discussed. The phase behavior, crystallization and microstructure of binary polystyrene blends of sPS/iPS and sPS/aPS with a specific composition of 5/5 weight ratio were investigated using optical microscopy (OM), differential scanning calorimetry, wide-angle X-ray diffraction, scanning and transmission electron microscopy (SEM and TEM). Based on the kinetics of enthalpy recovery, complete miscibility was found for the sPS/aPS blends where a single recovery peak was obtained, whereas phase separation was concluded for the sPS/iPS blends due to the presence of an additional recovery shoulder indicating the heterogeneity in the molten state. These findings were consistent with OM and SEM observations; sPS/iPS exhibits the dual interconnectivity of phase-separated phases resulting from spinodal decomposition.Both iPS and aPS have the same influence on the sPS crystal structure, i.e., dominant β-form sPS and mixed α-/β-form sPS obtained for melt-crystallization at high and low temperatures respectively, but imperfect α-form sPS developed when cold-crystallized at 175 °C. Co-crystallization of iPS and sPS into the common lattice was not observed regardless the thermal treatments, either cold or melt crystallization. Due to its slow process, crystallization of iPS was found to commence always after the completion of sPS crystallization in one-step crystallization kinetics. Segregation of rejected iPS component during sPS crystallization was extensively observed from TEM and SEM images which showed iPS pockets located between sPS lamellar stacks within spherulites, leading to the interfibrillar segregation, which was similar with that observed in the sPS/aPS blends. The addition of iPS (or aPS) component will reduce the overall crystallization rate of the sPS component and the retardation of crystal growth rates can be simply accounted by a dilution effect, keeping the surface nucleation intact. The phase-separated structure in the sPS/iPS blend shows a negligible effect on sPS crystallization and the signature of phase separation disappears after sPS crystallization. Depending on the relative dimensions of the segregated domains and iPS lamellar nucleus, subsequent crystallization of iPS can proceed to result in a crystalline/crystalline blend, or be inhibited to give a crystalline/amorphous blend morphology similar with that of sPS/aPS blends.     

Ultrasonic Spray Pyrolysis for Synthesis of Spherical Zirconia Particles

This paper presents new findings on ultrasonic spray pyrolysis of zirconium hydroxyl acetate precursor drops whose sizes were precisely measured using laser light diffraction technique. Precursor concentration plays a predominant role in determination of product particle size. At 0.01 wt% precursor concentration, conventional spray pyrolysis at 750°C using precursor drops 5–8 μm in diameter, generated by an ultrasonic nebulizer at 2.66 MHz, yielded uniform spherical yttria-stabilized zirconia (YSZ) particles 73 nm in diameter measured by scanning electron microscopy. The YSZ particle diameters were much smaller than those predicted by the one-particle-per-drop mechanism. Under similar reaction conditions, the high-throughput ultrasound-modulated two-fluid (UMTF) spray pyrolysis of larger precursor drops (28-μm peak diameter) also yielded spherical dense particles; they were significantly smaller in size than those produced by the low-throughput conventional ultrasonic spray pyrolysis of smaller drops (6.8-μm peak diameter).     

Growth of CeO2 Films on Sapphire and MgO by rf Magnetron Sputtering

pitaxial CeO₂ films on (1102) sapphire and (100) MgO were grown by rf magnetron sputtering. Substrate temperature, total pressure, and oxygen-to-argon mole ratio were varied to explore the optimal deposition condition. The X-ray diffraction spectra indicate that the degree of crystallinity of the deposited CeO₂ films depends on the oxygen- to-argon mole ratio and the substrate temperature. Atomic force microscopy images of the films on sapphire and MgO showed that substrate temperature and total pressure affect surface roughness. The best film surface is smooth with a 0.89 nm root-mean-square roughness. The quality of the films on MgO showed a strong dependence on substrate pretreatments. Epitaxial CeO₂ films could be grown on pre- annealed or pre-etched MgO if substrate temperatures reached higher than 790^deg;C. Additionally, the effect of ion bombardment at low total pressures on the crystallinity of the films was examined by growing the films outside the plasma region. Experimental results indicate that the ion bombardment does not prevent the films from preferred orientation.     

Fabrication of High-Curie-Point Barium-Lead Titanate PTCR Ceramics

High-Curie-point semiconducting barium-lead titanate positive temperature coefficient of resistivity (PTCR) ceramics of composition Ba_0.897Pb_0.1La_0.003TiO₃ and Ba_0.5Pb_0.5La_0.003TiO₃ were prepared. The starting powders were synthesized by reacting commercial BaTiO₃, PbO, and TiO₂. To avoid the nonstoichiometry due to the volatilization of Pb during the sintering process, a lead atmosphere sintering approach with PbTiO₃ as packing powder was used. The samples being fabricated by this method show a PTCR effect of 3 to 4.5 orders of magnitude above the Curie point. The curie points were about 180°C for Ba_0.897Pb_0.1La_0.003TiO₃ and about 360°C for Ba_0.497Pb_0.5La_0.003TiO₃.     

Morphology and characterization of conductive films based on polyaniline‐coated polystyrene latexes

The polyaniline (PANI)‐coated polystyrene (PS) latexes were synthesized, and the electrically conductive films were prepared thereafter. The weight ratio of PANI was 5%. Thermal analysis of the latices was performed using DSC and TGA. In this study, the electrically conductive films were prepared above the PS glass transition temperature (T_g). During the film formation, the effects of the annealing temperature and atmosphere (air or N₂) on the film resistance were investigated. In addition, the film morphology was observed utilizing scanning electron microscopy. The film resistance decreased in the initial heating stage due to the increasing temperature and the compaction of film. Then the film resistance increased with further annealing due to the aging of PANI. Typically, the film resistance was about 6000 Ω/sq, and the conductivity was 0.3 S/cm. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5406–5413, 2006     

Liquid-phase adsorption of dyes and phenols using pinewood-based activated carbons

Physical properties of activated carbons prepared from pinewood at different activation times (0.5, 1.5, 2.7, and 4.0 h) in steam at 900 °C were studied. The adsorption equilibria and kinetics of three dyes and three phenols (phenol, 3-chlorophenol, and o-cresol) from aqueous solutions on such carbons were then examined at 30 °C. The adsorption isotherms of phenols could be well fitted by the Freundlich equation, and those of dyes were adequately described by the Langmuir-Freundlich equation. The effect of microporosity of the carbons on adsorption capacity was explored. Four simplified kinetic models including pseudo-first-order equation, pseudo-second-order equation, intraparticle diffusion model, and the Elovich equation were selected to follow the adsorption processes. The adsorption of all six adsorbates could be best described by the Elovich equation. The kinetic parameters of this best-fit model were calculated and discussed.     

Identification of the combustion behaviour of lignite char between 350 and 900 °C

The combustion behaviour of four different lignite samples pyrolysed at 800 and 1000 °C has been studied. The reaction order and the activation energy of the char combustion reaction can be easily determined from the time to reach 50% conversion. Under 550 °C the reaction order of lignite samples are 0.7 and the activation energies are 27.4–27.9 kcal gmole^?1. Above 550 °C the measurement of the intrinsic reaction rate is limited by the film diffusion resistance. The pyrolysis temperature affects the reactivity significantly. The reactivity of char pyrolysed at 800 °C is 3.5 times that of char pyrolysed at 1000 °C.     

Influence of polymer molecular weight on selected thermodynamic properties of polymer/solvent systems and the application of the UNIFAC theory

The intrinsic viscosities of eleven narrow molecular weight distribution polystyrene samples ranging from number-average molecular weight 1820 to 1 292 000 have been determined in pure solvents of tetrahydrofuran and chloroform with a Ubbelohde No. 1 viscometer at 25°C. By combining the original and modified Fox-Flory viscosity treatments, respectively, with the Flory-Huggins Lattice theory, the interaction parameters were calculated. With the aid of original and modified UNIFAC methods the solvent activity, clustering function of the solvent, and the interaction parameter were computed and compared with the experimental data. It was established that the influence imposed by the polymer molecular weight on the activity of the solvent, the clustering function of solvent, and interaction parameter is insignificant. The modified UNIFAC method satisfactorily predicted the solvent activity as illustrated by previous investigators. However, both UNIFAC methods failed to predict the interaction parameter.