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51.
This report presents an investigation on the combustion of single droplets comprised of heavy oil and oil mixtures blending diesel light oil (LO) and a heavy oil residue (HOR). The tests were conducted in a microgravity facility that offered 10 s of free-fall time. Fine wire thermocouples supported the droplets, resulting in a measurement of droplet temperature history. Additional data were the droplet and flame size history. The results identified four distinctive burning stages between ignition and extinction for heavy oil (C class) and HOR-LO blends. They are, in succession, the start-up, inner evaporation, thermal decomposition (pyrolysis) and polymerization stages. The start-up stage denoted an initial transient period, where the LO components burned from the droplet surface and the droplet temperature increased rapidly. The latter three stages featured pronounced droplet swellings and contractions caused by fuel evaporation and decomposition inside the droplet. An evaporation temperature demarcated the start-up stage from the inner evaporation stage, and this temperature corresponded to a plateau in the temperature history of the droplet. Two additional temperatures, termed the decomposition and polymerization temperatures, indicated the ends of the evaporation and decomposition stages. These temperatures were similarly identified by plateaus or inflection points in the time-temperature diagram. The evaporation temperature gradually decreased with increasing the initial LO mass fraction in the droplet, whereas the other two temperatures were almost independent of the oil composition. All three temperatures increased with decreasing initial droplet diameter, but the dependence was very slight. Based on the results, the combustion of heavy oil droplets appears to be dominated by a distillation-like vaporization mechanism, because of the rapid mass transport within the droplets caused by the disruptive burning. 相似文献
52.
The forced convective heat transfer characteristics for incompressible power-law fluids past a bundle of circular cylinders have been investigated numerically. The cylinder-to-cylinder hydrodynamic interactions have been approximated via a simple cell model. The momentum and energy equations have been solved using a finite difference based numerical method for a range of physical and kinematic conditions. The role of the two commonly used thermal boundary conditions, namely, constant temperature or constant heat flux, on heat transfer characteristics has also been studied. Extensive numerical results elucidating the effect of shear-thinning viscosity on the values of Nusselt number have been obtained for Peclet numbers ranging from 1 to 5000, Reynolds number in the range 1-500, flow behaviour index 1?n?0.5 and three values of voidages, namely, 0.4, 0.5 and 0.6, typical of tubular heat exchangers and tube banks. Under all conditions, varying levels of enhancement in Nusselt number are observed due to shear-thinning behaviour. The surface averaged Nusselt number shows strong dependence on the values of voidage, power-law index, Reynolds and Peclet numbers. The paper is concluded by presenting comparisons with the scant experimental results available in the literature. 相似文献
53.
Two kinds of fly ash, discharged in the combustion of either refused derived fuel (RDF) or car shredder dust (SD), were examined for the emission of heavy metals in melting process under oxidizing and reducing conditions. The residual fractions of heavy metal in slag were experimentally estimated. As a result, it was confirmed that several volatile heavy metals were readily emitted during melting process. The type of atmosphere provided for the melting process was found to affect the emission of some volatile metals in RDF ash, but not in SD ash. The emission of volatile heavy metals in RDF ash under oxidizing conditions was lower than under any other conditions in this study. The emission behavior of iron and heavy metals in RDF ash under reducing conditions was similar to that in SD ash. These facts indicated that phosphorous in RDF ash had the property of fixing the volatile metals in the slag only under oxidizing conditions. Then the mixture of SD ash with phosphorous oxide powder was also tested in a melting process, and the result was consistent with the above inference of the effect of phosphorous. 相似文献
54.
离子液介质中生物催化与生物转化的研究进展 总被引:3,自引:0,他引:3
Ionic liquids have negligibly low vapor pressure, high stability and polarity. They are regarded as green solvents. Enzymes, especially lipases, as well as whole-cell of microbe, are catalytically active in ionic liquids or aqueous-ionic liquid biphasic systems. Up to date, there have been many reports on enzyme-exhibited features and enzyme-mediated reactions in ionic liquids. In many cases, remarkable results with respect to yield, catalytic activity, stability and (enantio-, regio-) selectivity were obtained in ionic liquids in comparison with those observed in conventional media. Accordingly, ionic liquids provide new possibilities for the application of new type of solvent in biocatalytic reactions. 相似文献
55.
Ammonium-based ionic liquid monomers and their corresponding polymers [poly(ionic liquid)s] are synthesized and characterized for CO2 sorption. The polymers have much higher CO2 sorption capacities than the room-temperature ionic liquids and imidazolium-based poly(ionic liquid)s. For example, P[VBTMA][PF6] with polystyrene backbone has a CO2 sorption capacity of 10.67 mol%. The CO2 sorption is selective over N2 and O2. The effects of cation, backbone, substituent, anion and crosslinking on CO2 sorption are discussed. The sorption mechanism study indicates that CO2 sorption by the poly(ionic liquid)s is a bulk and surface phenomenon. 相似文献
56.
57.
Mohammed Mahfooz Khan 《Fuel》1982,61(6):553-556
This Paper deals with a comparative study on the use of gel permeation chromatography (g.p.c.) and vapour pressure osmometry (v.p.o.) to obtain molecular weight data for the hexane-soluble fractions of three H-coal liquids. The use of two types of column packing materials, polyvinylacetate and styrene-divinylbenzene copolymer gels, is described. A successful, preparative use of the polyvinylacetate gel to fractionate the hexane-soluble fraction of H-coal liquid, atmospheric still overhead (ASO), has been established. Molecular weight data obtained by v.p.o. for the benzene-soluble fraction and the pyridine-soluble fraction of the three H-coal liquids are reported. Solvent extraction has been utilized also to find the amount of oil, asphaltenes and asphaltols in the three H-coal liquids. 相似文献
58.
T.V Malleswara Rao 《Chemical engineering science》2003,58(7):1365-1372
The steady flow of non-Newtonian polymer solutions on their own and together with air transverse to a bundle of circular rods, has been studied experimentally. In particular, the frictional pressure drop has been measured as a function of non-Newtonian power-law constants, flow rates, voidage of bundles and the input fraction of air over wide ranges of conditions as: power-law flow behaviour index, 0.5 to 1; voidage values of 0.78 and 0.87-0.88; air velocity (superficial), 0.09 to 0.28 m/s and liquid velocity (superficial) 0.018 to 0.5 m/s. While the single phase flow results for power-law liquids are in excellent agreement with an existing equation, the two-phase pressure drop results are also in accordance with the form of the well-known Lockhart-Martinelli correlation. Based on these results, it is suggested that a value of 5-10 for the Reynolds number based on rod diameter marks the limit of the laminar flow in such systems. 相似文献
59.
Hydrotreating of Maya heavy crude oil over high specific surface area CoMo/TiO2–Al2O3 oxide supported catalysts was studied in an integral reactor close to industrial practice. Activity studies were carried out with Maya crude hydrodesulfurization (HDS), hydrodemetallization (HDM), hydrodenitrogenation (HDN), and hydrodeasphaltenization (HDAs) reactions. The effect of support composition, the method of TiO2 incorporation, and the catalyst deactivation are examined. Supported catalysts are characterized by BET specific surface area (SSA), pore volume (PV), pore size distribution (PSD), and atomic absorption. It has been found that sulfided catalysts showed a wide range of activity variation with TiO2 incorporation into the alumina, which confirmed that molybdenum sulfided active phases strongly depend on the nature of support. The pore diameter and nature of the active site for HDS, HDM, HDN, and HDAs account for the influence of the large reactant molecules restricted diffusion into the pore, and/or the decrease in the number of active sites due to the MoS2 phases buried with time-on-stream. The textural properties and hysteresis loop area of supported and spent catalysts indicated that catalysts were deactivated at the pore mouth due to the metal and carbon depositions. The atomic absorption results agreed well regarding the textural properties of spent catalysts. Thus, incorporation of TiO2 with γ-Al2O3 alters the nature of active metal interaction with support, which may facilitate the dispersion of active phases on the support surface. Therefore, the TiO2 counterpart plays a promoting role to HDS activity due to the favorable morphology of MoS2 phases and metal support interaction. 相似文献
60.
李绿怡 《四川建材学院学报》2010,(2):90-92,99
采用电感耦合等离子体原子发射光谱法同时测定魔芋精粉中铅、铬、镉、砷、汞5种元素的含量,其检出限分别为0.0102、0.0009、0.001、0.028、0.004 mg.L-1,测定回收率在98.0%~103.0%之间,RSD(n=10)为0.5%~1.6%。所建立的元素分析方法其准确度和精密度均符合要求,应用本方法测定实际样品,结果令人满意。 相似文献