Flame chemical mechanism

They chemically interfere with the flame propagation mechanism. 

In Chapter 8.1, F. Takahashi presents candle and laminar jet diffusion flames highlighting fhe physical and chemical mechanism of combustion in a candle and similar laminar coflow diffusion flames in normal gravity and in microgravity. This apparently simple system turns out to be very complex, and thereby its study is of greaf importance for the understanding of diffusion flame fundamentals. 

The antimony oxide/organohalogen synergism in flame retardant additives has been the subject of considerable research and discussion over the past twenty-five years (1-17). In addition to antimony oxide, a variety of bismuth compounds and molybdenum oxide have been the subject of similar studies (18-20). Despite this intensive investigation, relatively little has been conclusively established about the solid state chemical mechanisms of the metal component volatilization, except in those cases where the organohalogen component is capable of undergoing extensive intramolecular dehydrohalogenation. 

Taing, S., A. R. Masri, and S. B. Pope (1993). PDF calculations of turbulent nonpremixed flames of H2/CO2 using reduced chemical mechanisms. Combustion and Flame 95, 133-150. 

The cool-flame phenomenon [15] is generally a result of the type of experiment performed to determine the explosion limits and the negative temperature coefficient feature of the explosion limits. The chemical mechanisms used to explain these phenomena are now usually referred to as cool-flame chemistry. 

To examine the effect of turbulence on flames, and hence the mass consumption rate of the fuel mixture, it is best to first recall the tacit assumption that in laminar flames the flow conditions alter neither the chemical mechanism nor the associated chemical energy release rate. Now one must acknowledge that, in many flow configurations, there can be an interaction between the character of the flow and the reaction chemistry. When a flow becomes turbulent, there are fluctuating components of velocity, temperature, density, pressure, and concentration. The degree to which such components affect the chemical reactions, heat release rate, and flame structure in a combustion system depends upon the relative characteristic times associated with each of these individual parameters. In a general sense, if the characteristic time (r0) of the chemical reaction is much shorter than a characteristic time (rm) associated with the fluid-mechanical fluctuations, the chemistry is essentially unaffected by the flow field. But if the contra condition (rc > rm) is true, the fluid mechanics could influence the chemical reaction rate, energy release rates, and flame structure. 

The term prompt NO derives from the fact that the nitrogen in air can form small quantities of CN compounds in the flame zone. In contrast, thermal NO forms in the high-temperature post-flame zone. These CN compounds subsequently react to form NO. The stable compound HCN has been found in the flame zone and is a product in very fuel-rich flames. Chemical models of hydrocarbon reaction processes reveal that, early in the reaction, O atom concentrations can reach superequilibrium proportions and, indeed, if temperatures are high enough, these high concentrations could lead to early formation of NO by the same mechanisms that describe thermal NO formation. 

Computational studies of partially premixed flames have also been reported [11-16], Authors have tried to explain the variation of NO emission indices with the level of partial premixing using one or more of the following residence time, flame stretch, radiation heat loss, and chemical mechanism-based arguments. However, a complete explanation of the NO emission has not been offered in the literature. 

The second is concerned with the need to have a complete and sensible chemical mechanism, valid over a wide range of temperature. Even a relatively simple combustion system will involve dozens of reactions, so that a well established reaction rate data base is essential. It is equivalently essential that the results be verified by comparison with detailed experimental data--such as that provided by laser probes. For example, in a study of the ozone decomposition flame (20). it was found that certain alternative but wrong choices of key input parameters were not discernible if flame speed were used as the sole predicted result for verification however, these choices did produce considerable differences in the profiles of the transient oxygen atom concentration and the temperature. 

Lewin M. Physical and chemical mechanisms of flame retarding of polymers. In Fire Retardancy of Polymers. The Use of Intumescence. Le Bras M, Camino G, Bourbigot S, Delobel R, Eds. Royal Society of Chemistry London, 1998 pp. 3-32. 

There are many different methods for modifying polymer surfaces to improve their adhesion and wetting properties. They include chemical etching and oxidation, ion bombardment, plasma treatments, flame treatment, mechanical abrasion and corona-discharge treatments (1.2). Especially flame and corona treatments are widely used for the modification of polyolefin surfaces to enhance, for instance, their printabilify. Despite the widespread use of such processes in industry, the understanding of the fundamental processes which occur at the polymer surface is very limited. This is undoubtedly due to the shallow depth to which the polymer is modified, typically 5 nm or less. 

The flame structure is modeled by solving the conservation equations for a laminar premixed burner-stabilized flame with the experimental temperature profile determined in previous work using OH-LIF. Three different detailed chemical kinetic reaction mechanisms are compared in the present work. The first one, denoted in the following as Lindstedt mechanism, is identical to the one reported in Ref. 67 where it was applied to model NO formation and destruction in counterffow diffusion flames. This mechanism is based on earlier work of Lindstedt and coworkers and it has subsequently been updated to include more recent kinetic data. In addition, the GRI-Mech. 2.11 (Ref. 59) and the reaction mechanism of Warnatz are applied to model the present flame. 

It is well known that good flame velocity results do not mean that the chemical mechanism is correct. Similarly, lists of reactions with high flame velocity sensitivity do not show all the important parameters of a flame mechanism. Tuning of rate parameters having high-flame velocity sensitivities would alter significantly the flame propagation speed, but there are other parameters in the mechanism which have to be known precisely for the calculation of realistic concentration vs. distance profiles. 

The pyrolysis products are mixed (block Mixer 1) and divided into two portions to ecd the so-called dense bed. The reactors Dense bed 1, Dense bed 2, and Flame 1 --lame 4 include extended chemical mechanisms describing the combustion of char, tar ind pyrolysis gases... 

In addition to the chemical mechanisms of fire retardants, thermal or barrier-type mechanisms may be operative. Coatings may prevent oxygen from reaching the wood surface. Dilution of combustible gases by noncombustible gases and inhibition of flaming by free radicals can also be in effect. Therefore, fire retardancy of wood involves many complex reactions. The effectiveness of a particular fire retardant depends on the overall summation of these competitive and sequential reactions and the thermal and physical environment of the material. 

In this chapter the experimental techniques used to obtain rate constants for the reactions of OH radicals with organics are described, and the resulting data and chemical mechanisms are presented. Discussion has been limited to data obtained at temperatures 6500 K, and hence flame, shock-tube, and hlgh-temperature thermal oxidation studies are not dealt with. 

Quantitative Chemical Mechanism for Heterogeneous Growth of Soot Particles in Premixed Flames... 

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