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Atomization secondary

Theoretical Considerations. A droplet generated in the primary atomization may be unstable and may further disintegrate [Pg.169]

Basic Breakup Modes. Starting from Lenard s investigation of large free-falling drops in still air,12671 drop/droplet breakup has been a subject of extensive theoretical and experimental studies[268] 12851 for a century. Various experimental methods have been developed and used to study droplet breakup, including free fall in towers and stairwells, suspension in vertical wind tunnels keeping droplets stationary, and in shock tubes with supersonic velocities, etc. These theoretical and experimental studies revealed that droplet breakup under the action of aerodynamic forces may occur in various modes, depending on the flow pattern around the droplet, and the physical properties of the gas and liquid involved, i.e., density, viscosity, and interfacial tension. [Pg.171]

According to Hinze,12701 droplet breakup may occur in three basic modes  [Pg.171]

The first mode may occur when a droplet is subjected to aerodynamic pressures or viscous stresses in a parallel or rotating flow. A droplet may experience the second type of breakup when exposed to a plane hyperbolic or Couette flow. The third type of breakup may occur when a droplet is in irregular flow patterns. In addition, the actual breakup modes also depend on whether a droplet is subjected to steady acceleration, or suddenly exposed to a high-velocity gas stream.[2701[2751 [Pg.171]

Subjected to steady acceleration, a droplet is flattened gradually. When a critical relative velocity is reached, the flattened droplet is blown out into a hollow bag anchored to a nearly circular rim which contains at least 70% of the mass of the original droplet. Surface tension force is sufficient to allow the bag shape to develop. The bag, with a concave surface to the gas flow, is stretched and swept off in the downstream direction. The rupture of the bag produces a cloud of very fine droplets presumably via a perforation mode, and the rim breaks up into relatively larger droplets, although all droplets are at least an order of magnitude smaller than the initial droplet size. This is referred to as bag breakup (Fig. 3.10)T2861 [Pg.172]


The overall requirement is 1.0—2.0 s for low energy waste compared to typical design standards of 2.0 s for RCRA ha2ardous waste units. The most important, ie, rate limiting steps are droplet evaporation and chemical reaction. The calculated time requirements for these steps are only approximations and subject to error. For example, formation of a skin on the evaporating droplet may inhibit evaporation compared to the theory, whereas secondary atomization may accelerate it. Errors in estimates of the activation energy can significantly alter the chemical reaction rate constant, and the pre-exponential factor from equation 36 is only approximate. Also, interactions with free-radical species may accelerate the rate of chemical reaction over that estimated solely as a result of thermal excitation therefore, measurements of the time requirements are desirable. [Pg.56]

The intrinsic drawback of LIBS is a short duration (less than a few hundreds microseconds) and strongly non-stationary conditions of a laser plume. Much higher sensitivity has been realized by transport of the ablated material into secondary atomic reservoirs such as a microwave-induced plasma (MIP) or an inductively coupled plasma (ICP). Owing to the much longer residence time of ablated atoms and ions in a stationary MIP (typically several ms compared with at most a hundred microseconds in a laser plume) and because of additional excitation of the radiating upper levels in the low pressure plasma, the line intensities of atoms and ions are greatly enhanced. Because of these factors the DLs of LA-MIP have been improved by one to two orders of magnitude compared with LIBS. [Pg.234]

These are particularly applicable to burners firing the heavier grades of oil which contain long-chain molecules called asphaltines. The superheating of the water in the emulsified fuel droplet enhances atomization. The effect is to provide secondary atomization to the droplet as the steam is formed. [Pg.378]

In contrast to Ag, these emission profiles are insensitive to variations of the excitation wavelength within the threefold structure of the 2P 2S absorption band. Simultaneous with the photolysis of any of the three 2P - 2S components, one observes gradual bleaching of all lines with concurrent formation of Ci where n =2-5 (34,56). A further intriguing observation concerns the appearance of a weak structured emission near 420 nm for excitations centered on the secondary atomic site band of Cu in all three rare gas films (Figure 4), which has been found from independent studies of the absorption and emission spectra of matrix entrapped CU2 to arise from the A-state of CU2 (34). [Pg.304]

Secondary atomization, the breakup of the drops first formed, has been studied by Littaye (11C), who assumes a necessary criterion that the drag forces exceed the inertia forces. Ohnesorge (17C) makes use of the principles of mechanical similarity by introducing dimensionless coefficients to help explain jet breakup. Above certain well defined numbers, the jet completely atomizes at the nozzle. Lower values indicate the formation of a jet which disintegrates, owing to helical vibrations which later change into Rayleigh vibrations. [Pg.141]

The way to understand the first step in the formation of a molecule is to consider a given atom as surrounded by a number of non-interacting secondary atoms, or ligands. The energy and o-a-m of the central atom is affected by the presence of the coordination shell of ligands, within the demands of the relevant conservation laws. Their effect can be simulated by recalculation of the electronic energy and o-a-m of the central atom in the modified symmetry environment, defined by the distribution and nature of the ligands. [Pg.223]

In an attempt to modify the observed droplet behavior, a brief qualitative investigation was carried out with blends of SRC-II heavy distillate and pure heptane. The objective was to enhance droplet disruptive combustion as a means of reducing effective droplet size and hence soot formation. With these fuels visible droplet fragmentation was found to occur throughout the droplet stream. The fragmentation produced new droplets on different trajectories these in turn were terminated by small disruptions, as described above. Three blends were used 60/40, 80/20, and 90/10. Secondary atomization was observed for all three, although the violence of the activity was noticeably reduced as the heptane content of the blend became smaller. This secondary atomization was a completely different process than the... [Pg.199]

Secondary atomic properties as those, which require, in addition to the experimentally determined quantities for the free atoms, theoretical concepts of the quantum mechanical characerisation of the electronic structure of the atoms. These are orbitals, the shell structure of atoms with emphasis of the valence shell as well as concepts like hybridisation, the definition of the valence state and the valence state promotion energy in its relation to the spectroscopic term values of the free atoms. [Pg.192]

Clearly, the atomic electronegativities, as defined and determined following the suggestions of Pauling, would in this classification be characterised as tertiary atomic properties. On the other hand, primary and, as theoretical concepts will in general be required, secondary atomic properties are to be preferred, when molecular properties are to be derived qualitatively or semiquantitatively on the basis of the properties of the constituent atoms. [Pg.192]

Measurements have been made of the combustion characteristics of an air blast kerosene spray flame and of droplet sizes within the spray boundary of isothermal sprays. Specific techniques were used to measure velocity, temperature, concentration, and droplet size. Velocities measured by laser anemometer in spray flames in some areas are 400% higher than those in isothermal sprays. Temperature profiles are similar to those of gaseous diffusion flames. Gas analyses indicate the formation of intermediate reactants, e.g., CO and Hg, in the cracking process. Rosin-Rammler mean size and size distribution of droplets in isothermal sprays are related to atomizer efficiency and subsequent secondary atomizer/vaporization effects. [Pg.111]

Emulsified fuels can undergo secondary atomization in combustion systems as a result of heating and expansion of the internal (dispersed) phase. [Pg.243]

Data for the specific rate coefficients for abstraction from CH bonds have been derived from experiments with hydrocarbons with different distributions of primary, secondary, and tertiary CH bonds. A primary CH bond is one on a carbon that is only connected to one other carbon, that is, the end carbon in a chain or a branch of a chain of carbon atoms. A secondary CH bond is one on a carbon atom connected to two others, and a tertiary CH bond is on a carbon atom that is connected to three others. In a chain the CH bond strength on the carbons second from the ends is a few kilojoules less than other secondary atoms. The tertiary CH bond strength is still less, and the primary is the greatest. Assuming additivity of these rates, one can derive specific reaction rate constants for abstraction from the higher-order hydrocarbons by H, O, OH, and HO2 [31]. [Pg.98]

Due to the sputtering process an incoming ion beam ejects secondary atoms and ions from the surface. The secondary ions may be analysed by means of a mass spectrometer (SIMS). [Pg.40]

Pneumatic nozzles prevail, but the spray pattern is somewhat different than found in a fluidized bed. In air suspension systems, the spray is usually a comparatively narrow, but solid cone of droplets. In a nozzle configured for perforated pan coating equipment, the initial spray pattern is also a solid cone. However, this pattern is flattened to an elliptical. shape by the u.se of. secondary atomizing air, delivered from openings adjacent to and angled slightly toward the primary atomized droplet stream (Fig. 10). In most nozzles, this secondary air is adjusted and controlled independently. The nozzle is... [Pg.372]

Mathematically, this implies that while the primary zone s atoms may feel very anharmonic S-S forces and feel the force from the AB molecule, the secondary zone can be described by simple harmonic S-S restoring forces and should be relatively independent of the forces due to the AB molecule. Solving for the motion of the harmonic secondary atoms and substitution of this result into the equations of motion of the primary zone atoms yields a GLE for the latter ... [Pg.213]

The choice of methods is a matter of convenience. Both will capture the essential features of the GLE, namely frictional energy loss from the primary atoms to the secondary atoms and thermal energy transfer from the secondary atoms to the primary atoms. Both will provide a reasonable description of the bulk and surface phonon density of states of the solid. Neither will provide the exact time-dependent response of the solid due to the limited number of parameters used to describe the memory function. [Pg.215]

Current spray models may not have the correct physics, may have unknown limits of applicability, and may contain empirical constants. In a recent test conducted by the author and United Technologies Research Center (UTRC), models of primary atomization, secondary atomization, droplet breakup, droplet collision, and turbulent dispersion were applied to an air blast spray. The predictions were compared to experimental data taken at UTRC. The predicted drop size was as much as 35% different from the measured values [8]. In contrast to the typical conference or journal publication, the models were not adjusted to make the agreement as close as possible. They were taken from the literature as is. The conclusion is that physical models of high-speed spray behavior are still lacking, despite years of research in this area. Primary atomization, the beginning of the spray, is one area that is particularly poorly understood. [Pg.40]

Two important elementary step reactions were described in these radical chains of Rice. One was the ubiquity of the metathetical reaction of H atom abstraction by free radicals from hydrocarbons. The second was the rapid unimolecular decomposition of free radicals into olefins and secondary atoms or radicals, as a chain step competitive with metathesis. [Pg.9]

An alloy is a mixture of two or more materials, at least one of which is a metal. Alloys can have a microstructure consisting of solid solutions, where secondary atoms are introduced as substitutionals or interstitials (discussed further in the next chapter and Module 5, Plant Materials) in a crystal lattice. An alloy might also be a crystal with a metallic compound at each lattice point. In addition, alloys may be composed of secondary crystals imbedded in a primary polycrystalline matrix. This type of alloy is called a composite (although the term "composite" does not necessarily imply that the component materials are metals). Module 2, Properties of Metals, discusses how different elements change the physical properties of a metal. [Pg.33]

Solid solutions, where secondary atoms introduced as substitutionals or interstitials in a crystal lattice. [Pg.35]


See other pages where Atomization secondary is mentioned: [Pg.330]    [Pg.445]    [Pg.122]    [Pg.133]    [Pg.145]    [Pg.169]    [Pg.169]    [Pg.322]    [Pg.381]    [Pg.121]    [Pg.61]    [Pg.106]    [Pg.57]    [Pg.108]    [Pg.187]    [Pg.200]    [Pg.489]    [Pg.194]    [Pg.208]    [Pg.61]    [Pg.237]    [Pg.243]    [Pg.1796]    [Pg.2095]    [Pg.14]    [Pg.214]    [Pg.181]   
See also in sourсe #XX -- [ Pg.122 , Pg.133 , Pg.145 , Pg.169 ]

See also in sourсe #XX -- [ Pg.38 ]




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