Investigation of the Effect of DOP on Polyaniline and Polyaniline/Polystyrene Nanocomposites

Polyaniline nanocomposite was prepared in aqueous media by polymerization of aniline using ((NH₄)₂S₂O₈) as an oxidant in the presence of dioctyl phthalate (DOP). Also polyaniline/polystyrene (PAn/PS) nanocomposite was prepared in the aqueous solution by polymerization of styrene and aniline using potassium iodate (KIO₃) and ammonium peroxy disulfate ((NH₄)₂S₂O₈) as oxidant in the presence of dioctyl phthalate (DOP). The PAn and PAn/PS nanocomposites were characterized in terms of morphology, chemical structure and glass transition temperature. The chemical structure, morphology and glass transition temperature of product were studied by Fourier Transform Infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and differential scanning calorimetry (DSC).     

Significance of Acoustic and Hydrodynamic Cavitations in Enhancing Ozone Mass Transfer

Assessment of both acoustic and hydrodynamic cavitations for intensifying ozone mass transfer was conducted simultaneously. Four process schemes were arranged to evaluate the effect of application of each kind of cavitation as well as both of them, on the ozone mass transfer process. All processes were conducted at pH of 3 to avoid ozone natural self-decomposition initiated by hydroxide ions (OH^?). The chemical and mechanical effects of cavitation were distinguished by using radical scavengers to suppress radical formation. The result showed that hydrodynamic and acoustic cavitations enhanced ozone mass transfer synergistically. The enhancement obtained from the acoustic cavitation was higher than that obtained from the hydrodynamic cavitation, and the chemical effects of cavitation were much significant than that of mechanical effects. The enhancement obtained due to chemical effects of cavitation was about twice the enhancement obtained due to mechanical effects when only one type of cavitation was combined with ozonation. Combination of both type of cavitation and ozonation gave the enhancement obtained due to chemical effect of 3.68 times that obtained due to mechanical effects.     

Sensitivity to change in laminar burning velocity and Markstein length resulting from variable hydrogen fraction in blast furnace gas for changing ambient conditions

The sensitivity to changes in fuel characteristics has been investigated for combustion of Blast Furnace Gas resulting from small volumetric increases in H₂ concentration. A nonlinear methodology has been employed to quantify unstretched flame speeds and the effect of flame stretch from outwardly propagating spherical flames. Following benchmarking work with CH₄, results were obtained under ambient conditions of 303 K and 0.1 MPa, with small absolute change in hydrogen concentration shown to at least triple the laminar burning velocity for all tested mixtures. Fuel composition and equivalence ratio were shown to independently influence mixture diffusivity and Lewis number, quantified by change in the obtained values of Markstein length. Temperature and pressure were increased to respective values of 393 K and 0.2 MPa to investigate influence of ambient conditions, with a power law correlation presented. Finally the performance of several published chemical reaction mechanisms has been evaluated through comparison of 1-D flame models.     

Thermodynamic assessment of hydrogen production and cobalt oxidation susceptibility under ethanol reforming conditions

A comparative thermodynamic analysis of ethanol reforming reactions was conducted using an in-house code. Equilibrium compositions were estimated using the Lagrange multipliers method, which generated systems of non-linear algebraic equations, solved numerically. Effects of temperature, pressure and steam to ethanol, O₂ to ethanol and CO₂ to ethanol ratios on the equilibrium compositions were evaluated. The validation was done by comparing these data with experimental literature. The results of this work proved to be useful to foresee whether the experimental results follow the stoichiometry of the reactions involved in each process. Mole fractions of H₂ and CO₂ proved to be the most reliable variables to make this type of validation. Maximization of H₂ mole fraction was attained between 773 and 873 K, but maximum net mole production of H₂ was only achieved at higher temperatures (>1123 K). This work also advances in the thermodynamics of solid-gas phase interactions. A solid phase thermodynamic analysis was performed to confirm that Co⁰ formation from CoO is spontaneous under steam reforming conditions. The results showed that this reduction process occurs only for temperatures higher than 430 K. It was also found that once reduced, Co based catalysts will never oxidize back to Co₃O₄.     

Magnetic held dependence of elastic modulus and resistance in La2/3Ca1/3MnO3

We have measured the magnetic field dependence of the anelastic modulus and the electric resistance of a ceramic sample of the magnetoresistant perovskite La_2/3Ca_1/3MnO₃ around the metal–insulator transition by the vibrating reed technique (2.5 KHz). Previous work [1] showed that the modulus becomes higher while the internal friction has a peak at the transition temperature (T_c=262 K). In this work, improvements made on the equipment allowed us to measure at constant deformations (<10⁻⁵) and magnetic fields up to 4500 Gauss. We made isothermal measurements of internal friction, modulus and resistance as a function of an applied magnetic field. We found that most of the changes induced by the magnetic field take place in a few degrees (almost 5 K) near the transition temperature where the changes in resistance are more important. Up to the highest magnetic field applied, we found 3% maximum variations of the modulus and no hysteresis while cycling the magnetic field. We suppose that the experiment is placed in the linear response of the inverse Wiedemann effect [2], due to the small deformations used, and that the ferromagnetic domain structure is responsible for the observed effects. Some additional measurements are needed (magnetic hysteresis loops) to be compared with our results.     

处理废碱液中硫化物和有机物的方法研究

本文主要研究用化学催化氧化和光学氧化相结合的方法处理废碱液中所含的高浓度硫化物和有机物 ,并研究各影响因素的作用情况。实验结果表明 ,硫化物的转化率随反应温度升高、反应时间的延长而增大 ;而且当反应温度 6 0℃ ,曝气量 0 6m3 /h、Mn2 初始浓度 15mg/L、反应时间 90min时 ,硫化物的转化率为 95 3%。COD的去除率随反应时间的延长而增大 ;反应时间 15 0min时 ,COD的去除率即可达到6 5 2 %     

Enhancing effect of monoolein surfactant on carbon nanoparticle synthesis by arc discharge in liquid

Effect of monoolein surfactant which promotes n-hexane to dissolve in water was investigated to enhance the carbon nanoparticle (CNP) synthesis by arc discharge in liquid. The production rate of CNPs consisting of multi-shelled fullerenes and multi-walled carbon nanotubes was increased by the addition of the n-hexane to water with support of monoolein surfactant. An optimal amount of monoolein led to the maximal production rate of CNPs which was ca. two-fold higher than that obtained from a pure water system. This effect is ascribed to the role of n-hexane and monoolein to provide carbon clusters to the arc reactive zone. The hydrodynamic particle sizes of CNPs and their crystallinity were also enhanced by the addition of these organic compounds. As the vapor pressure of the organic component is significantly suppressed, the proposed method is much safer than that using pure organic liquid.     

High-resolution X-ray photoelectron spectroscopy study of InTe thin film in structural phase transition from amorphous to crystalline phase

We investigated the chemical states of InTe thin film in the structural phase transition from the amorphous to the crystalline phase, using high-resolution X-ray photoelectron spectroscopy with synchrotron radiation. We confirmed the structural phase transition by transmission electron microscopy. Clean amorphous InTe (a-InTe) free of oxygen impurity was obtained after Ne⁺ ion sputtering at the ion beam energy of 1 kV for 1 h. Additionally, we obtained crystalline InTe (c-InTe) from clean a-InTe by annealing at 250 °C in an ultra-high vacuum. During the transition to the crystalline phase, the binding energy of the Te 4d core-level was unchanged, but the peak width was somewhat wider than in the amorphous phase. In the case of the In 4d core-level, the chemical shift was 0.1 eV at the higher binding energy between the amorphous and crystalline phases. The valence band maximum was shifted at the higher binding energy of 0.34 eV. We assumed that the Te atom was almost fixed and that the In atoms moved in the tight binding energy state to the center of the 4-Te atoms.     

Chemical reagents as probes: Application to fish protein gels and detection of a cysteine TGase in hake

A new concept was applied to fish products. Chemical reagents targeting specific chemical bonds were incorporated in to gel products for assessing the importance of non-covalent (sodium dodecylsulphate, 1.0%, w/w), disulphide (dithiothreitol, 0.2%, w/w) or transglutaminase-catalyzed (N-ethylmaleimide, 0.2%, w/w) bonding. These reagents acting as chemical probes were applied to the study of sea bass and hake protein gels and the effect of MTGase (0.5%, w/w).These reagents were valuable for reaching conclusions. The action of an endogenous cysteine TGase in hake products was detected. It was found that frozen storage and protein denaturation are fundamental not only for explaining differences between raw materials, but also seem to favour a different action mode of MTGase in each raw material. Moreover, this study may help to improve processed products, for instance, the positive interaction between MTGase and the disruption of disulphide bonds in hake gels may find a useful application through incorporation of cysteine + MTGase.     

Chemical composition and physical properties of black liquors and their effects on liquor recovery operation in Brazilian pulp mills

Black liquor is the major by-product and fuel of pulp mills. In this work, effects of black liquor properties on its recovery unit operation are analyzed. Thus, an experimental methodology for characterizing the principal chemical and physical properties of eucalyptus Kraft and bamboo soda black liquors has been developed, including sample collections from six Brazilian mills. Based on results, eucalyptus and bamboo black liquors present higher contents of non-processing elements (NPEs), higher concentration and different molar mass of lignin than those reported by the pine Kraft black liquor. This leads to distinct rheological properties of these liquors. By comparing results obtained for the both liquors, the bamboo and the eucalyptus, the former has the lowest sulfur level, the highest silicon and lignin concentration and, consequently, the highest apparent viscosity.