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51.
A non-steady boundary layer model is developed for numerical simulation of combustion and gasification of a single shrinking char particle. The model considers mass and energy conservation coupled with heterogeneous char reactions producing CO and homogeneous oxidation of CO to CO2 in the boundary layer surrounding the char particle. Mass conservation includes accumulation, molecular diffusion, Stefan flow and generation by chemical reaction. Energy conservation includes radiation transfer at the particle surface and heat accumulation within the particle. Simulation results predict experimentally measured conversion and temperature profiles of a burning Spherocarb particle in a laminar flow reactor. Effects of bulk oxygen concentration and particle size on the combustion process are addressed. Predicted particle temperature is significantly affected by boundary layer combustion of CO to CO2. With increasing particle size, char gasification to char combustion ratio increases, resulting in decreasing particle temperature and increasing peak boundary layer temperature. 相似文献
52.
Epoxy resin is chosen for our present study owing to its exceptional combination of properties such as easy processing, high safety, excellent solvent and chemical resistance, toughness, low shrinkage on cure, good electrical, mechanical and corrosion resistance with excellent adhesion to many substrates. This versatility in formulation made epoxy resins widely applied for surface coatings, adhesives, laminates, composites, potting, painting materials, encapsulant for semiconductor and insulating material for electric devices. There are numerous paint/coating systems based on epoxy resin available for corrosion and fouling prevention. They however are not completely satisfactory in field applications, where high corrosion, fouling and flame resistance are required. The demand for epoxy resin as corrosion/fouling resistant coatings is restricted mainly due to its inferior characteristics like poor impact strength, high rigidity, and moisture absorbing nature besides inadequate flame retardant properties. It is for this reason that silicones and phosphorus-based compounds are used as modifier in this work by intercrosslinking network mechanism (ICN) to obtain epoxy resin with desired properties ideally suitable for field applications for preventing corrosion and fouling with flame retardantancy. The present work involves the development of solvent free silicone/phosphorus modified epoxy coating systems, since solvent free coating systems are widely used for numerous applications due to their lower cost per unit film thickness, freedom from fire and pollution hazard and ability to provide better performance. For the development of coating systems, epoxy resin (X) serves as base material, hydroxyl terminated polydimethylsiloxane (HTPDMS) as modifier, γ-aminopropyltriethoxysilane (γ-APS) as crosslinking agent and dibutyltindilaurate (DBTDL) as catalyst. Polyamidoamine (A), aromatic amine adducts (B) and phosphorus-containing diamine (C) were used as curing agents. The study also describes the evaluation of corrosion resistant behaviour of unmodified epoxy and siliconized epoxy coatings by potentiodynamic polarization method, electrochemical impedance spectroscopy (EIS), salt-spray and antifouling tests. The results are discussed. 相似文献
53.
This work provides kinetic and transport parameters of Li-ion during its extraction/insertion into thin film LiNi0.5Mn1.5O4 free of binder and conductive additive. Thin films of LiNi0.5Mn1.5O4 (0.2 μm thick) were prepared on electronically conductive gold substrate utilizing the electrostatic spray deposition technique. High purity LiNi0.5Mn1.5O4 thin film electrodes were observed with cyclic voltammetry, to exhibit very sharp peaks, high reversibility, and absence of the 4 V signal related to the Mn3+/Mn4+ redox couple. The electrode subjected to 100 CV cycles of charge/discharge delivered a capacity of 155 mAh g−1 on the first cycle and sustained a good cycling behavior while retaining 91% of the initial capacity after 50 cycles. Kinetics and mass-transport of Li-ion extraction at LiNi0.5Mn1.5O4 thin film electrode were investigated by means of electrochemical impedance spectroscopy. The apparent chemical diffusion coefficient (Dapp) value determined from EIS measurements changed depending on the electrode potential in the range of 10−10-10−12 cm2 s−1. The Dapp profile shows two minimums at the potential values close to the peak potentials of the corresponding cyclic voltammogram. 相似文献
54.
Using TiO2 as carrier, CuO/TiO2 catalysts with different CuO loading were prepared by the impregnation method. The catalytic activities in NO+CO reaction
were examined with a micro-reactor gas chromatography reaction system and the methods of TPR, XPS and NO-TPD. It was found
that the catalytic activities were affected by pretreatment atmosphere, i.e. H2 atmosphere > reduction–reoxidation > 10%CO/He > reaction gas (fresh sample). NO decomposition was better by low-valence Cu
species than by high-valence Cu species, i.e. Cu0>Cu+>Cu2+. The XPS results indicated that Cu species on CuO/TiO2 were Cu0, Cu+, normal Cu2+(Cu2+(I)) and chain-structured Cu2+(Cu2+(II)) as –Cu–O–Ti–O–. The activities of Cu2+(II) were much higher than that of Cu2+(I), but both species were very unstable in the reaction atmosphere and easily reduced by CO, which accounted for the variable
activities of fresh catalysts with increasing reaction temperature. In NO+CO reaction, the redox process was a cycle of Cu+–Cu2+(I) at low reaction temperature but was a cycle of Cu0–Cu+ at high reaction temperature. As shown by NO-TPD, high catalytic activities could be attributed to the following factors,
e.g. oxygen caves on the catalyst’s surface after pretreatment with H2 and reduction–reoxidation, formation of Cu0 after pretreatment with H2, and increment of Cu species dispersion and formation of Cu2+(II) after pretreatment with reduction–reoxidation. 相似文献
55.
LiNi1/3Co1/3Mn1/3O2 cathode materials have been coated with Al2O3 nano-particles using sol-gel processing to improve its electrochemical properties. The X-ray diffraction (XRD) pattern of the as-prepared Al2O3 nano-particles was indexed to the cubic structure of the γ-Al2O3 phase and had an average size of ∼4 nm. The XRD showed that the structure of LiNi1/3Co1/3Mn1/3O2 was not affected by the Al2O3 coating. However, the Al2O3 coatings on LiNi1/3Co1/3Mn1/3O2 improved the cyclic life performance and rate capability without decreasing its initial discharge capacity. These electrochemical properties were also compared with those of LiAlO2-coated LiNi1/3Co1/3Mn1/3O2 cathode material. The electrochemical impedance spectroscopy (EIS) was studied to understand the enhanced electrochemical properties of the Al2O3-coated LiNi1/3Co1/3Mn1/3O2 compared to uncoated LiNi1/3Co1/3Mn1/3O2. 相似文献
56.
The quantitative aspects of the role of interfacial mass-transfer and reaction kinetics in ethoxylation of lauryl alcohol were examined in a batch recirculation reactor. The liquid droplets falling through a gas column were obtained by utilizing a recirculation loop and a set of spray nozzles. The CO2/NaOH reaction was employed to characterize the interfacial area. The alkoxylation reaction was studied at temperatures between 124°C and 171°C, at catalyst levels between 0.09 and 0.50 weight percent and at ethylene oxide partial pressures between 68 kPa and 204 kPa. A model was developed which permits the prediction of reactor performance at various operating conditions. The mass-transfer during free fall dominates the interfacial mass-transfer and the contributions during the drop formation and coalescence stages are small. The rate of ethylene oxide (EO) addition to lauryl alcohol was constant during the batch run, indicating similar activity for the unreacted lauryl alcohol and the lauryl alcohol ethoxylated to varying extents. The rate of ethoxylation is first-order in both catalyst and ethylene oxide concentrations. The liquid-phase reaction kinetics and interfacial mass-transfer occur in series, with kinetics dominating the overall ethoxylation rate. As expected, an increasing role of mass transfer is observed at higher temperatures, and/or higher catalyst concentrations where the kinetic rate becomes significantly high. The intrinsic activation energy for the ethoxylation of lauryl alcohol is 55.2 kJ/mole. 相似文献
57.
Francesca Guidi Giovanni Carta Gilberto Rossetto Guido Salmaso 《Electrochimica acta》2005,50(23):4609-4614
Alumina (Al2O3) coatings of different thickness were deposited on OT59 brass substrate (BS) using the metal organic chemical vapour deposition (MOCVD) technique to evaluate the corrosion performance by EIS measurements. The used precursor was dimethyl-aluminium-isopropoxide. Electrochemical characterizations of the deposited films were performed in a standard very aggressive acidic solution (aerated 1N H2SO4 at 25 °C up to 168 h of immersion time) by means of direct current method (Tafel curves) and electrochemical impedance spectroscopy (EIS). The Rutherford backscattering spectroscopy (RBS) indicated that the films are very pure with the correct Al2O3 stoichiometry, while the IR absorption spectra showed that the films did not contain any OH groups. The surface film morphology was investigated by atomic force microscopy (AFM) and displayed a globular texture. The films were very smooth, with a maximum root mean square roughness, for example, of 14 nm for a 0.96 μm thick coating. The EIS data confirmed, as expected, that a 2.40 μm Al2O3 layer ensures the best corrosion protection after 168 h of immersion in the very acidic environment used. 相似文献
58.
Ying Wang 《Electrochimica acta》2006,51(23):4865-4872
Thin films of orthorhombic V2O5 have been prepared by sol electrophoretic deposition (EPD) followed by post-treatment at 500 °C. Their electrochemical and optical performances have been investigated for possible applications in electrochemical/electrochromic devices. Li+-intercalation properties of the films have been explored in two voltage ranges: 0.4 to −1.1 V and 0.4 to −1.6 V versus Ag/Ag+, respectively. High capacities of over 300 mAh/g are acquired in the wider voltage range at a current density of 50 μA/cm2 and moderate capacities of 140 and 110 mAh/g are obtained in the narrower voltage range at a current density of 25 and 50 μA/cm2, respectively. Electrochemical measurements have shown that the films demonstrate good cyclability in both voltage ranges. X-ray diffraction, scanning electron microscopy and optical spectra have been used to examine the changes in crystallinity, microstructure, morphology and transmittance of the films during cycling. Films cycled to a deeper voltage of −1.6 V versus Ag/Ag+ deliver higher capacity with appreciable morphological change, while films cycled in the narrower voltage range show moderate capacity and maintain the morphology, optical responses and crystalline structure. Voltage range can be optimized in between to acquire both high capacity and stability in structure, electrochemical and optical properties. High Li+-intercalation capacity and good cyclic stability are attributed to the porous structure of V2O5 films prepared by EPD. 相似文献
59.
60.
Utilising a pseudo-reference electrode in polymer electrolyte fuel cells allows for the separation of anodic and cathodic contributions to the entire cell impedance. Modelling the impedance responses by using equivalent circuits inhibits the investigation of kinetic parameters of the basic electrochemical reactions, which take place at single electrode-electrolyte interfaces. Therefore, we evaluate single electrode impedance measurements by a kinetic model, which is based on specific reaction pathways, either for the oxygen reduction reaction (ORR) or the hydrogen oxidation reaction (HOR). As a consequence, it is possible to obtain kinetic parameters for the specific reaction of interest. Furthermore, the information gained from the single electrode impedance measurements and the kinetic model can give insight into single reactions steps. In particular, the ORR has to include a chemical step in the reaction pathway. 相似文献