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The Case of Combustion

But as one man would show, scientific theories do not always stand the test of time. [Pg.286]

By 1700, combustion was assumed to be the decomposition of a material into simpler substances. People saw burning substances emitting smoke and energy as heat and light. [Pg.286]

To account for this emission, scientists proposed a theory that combustion depended on the emission of a substance called phlogiston (Greek, meaning burned ), which appeared as a combination of energy as heat and light while the material was burning but which could not be detected beforehand. [Pg.286]

The phlogiston theory was used to explain many chemical observations of the day. For example, a lit candle under a glass jar burned until the surrounding air became saturated with phlogiston, at which time the flame died because the air inside could not absorb more phlogiston. [Pg.286]

By the 1770s, the phlogiston theory had gained universal acceptance. At that time, chemists also began to experiment with air, which was generally believed to be an element. [Pg.286]


The uptake of heavy metals from soils is also determined by their contents in soil and by plant species. If these crops are used for anaerobic digestion one has to consider that there is a remarkable risk of an accumulation of heavy metals in soil. In the case of combustion, most heavy metals can be removed by filtering the ash and it can be used safely as fertiliser. Thus cultivation and combustion of short rotation coppice is a smart scheme of removing heavy metals from contaminated soils. [Pg.110]

The case of combustion of an entire spherical surface with forced convection has not yet been solved. Frossling (4) originally proposed a semi-empirical relation for the low-temperature evaporation of droplets in motion. Spalding (60) has applied the equation to his heterogeneous combustion data with some success by including the term containing the transfer number ... [Pg.122]

At the limit in an infinitely rapid reaction a and 6 in the reaction zone tend to zero so that nowhere (except in an infinitely narrow zone) can a and b be simultaneously nonzero. Thus, in the case of combustion, by finding the distribution of p in space from the solution of the Unear equation (15) with conditions (16), we easily find the fields for a and b as well ... [Pg.308]

In the case of combustion of a condensed substance, conservation of enthalpy and similarity occur only in the gas phase and only in part of the space. In the c-phase the diffusion coefficient is much smaller than the thermal diffusivity, and we have heating of the c-phase by heat conduction without dilution by diffusion. The enthalpy of the c-phase at the boundary, for x — 0 (from the side x < 0), is larger than the enthalpy of the c-phase far from the reaction zone and larger than the enthalpy of the combustion products. The advantage of the derivation given here is that the constancy of the enthalpy in the gas phase and its equality to H0 (H0 is the enthalpy of the c-phase far from the combustion zone, at x — —oo) are obtained without regard to the state of the intermediate layers of the c-phase. We should particularly emphasize that the constancy of the enthalpy in the combustion zone occurs only for a steady process. The presence of layers of the c-phase with increased enthalpy opens the possibility in a non-steady process of a temporary change in the enthalpy of the gas and the combustion temperature (on this see 5). [Pg.341]

In the case of combustion of a liquid EM a change in the aggregate state causes a sharp jump in its properties for constant temperature. The volume rate of heat release in a gas monotonically falls with decreasing temperature, beginning from a temperature close to TB. At TB, in the transition from a gas to a liquid, the volume rate of heat release increases sharply, discontinuously, due to the sharp increase in the density. As the temperature is lowered further, the density of the liquid remains constant and the volume rate of heat release again falls according to Arrhenius law of the dependence of temperature on the reaction rate. [Pg.346]

In the case of combustion of condensed substances, consideration of nonsteady processes, accounting for the non-adiabatic nature of combustion, which we do not present here, leads to the following conclusions ... [Pg.357]

The scintillator Permafluor E+ recommended by Canberra-Packard for their automatic combusters was used in the case of combusted samples. The scintillator Roth-rotiszint eco plus (Roth, Karlsruhe, Germany) was used for the samples measured directly. [Pg.586]

When all reactants and products are condensed phases, the A p ) term is negligible in comparison with AH or AE, and the distinction between these two quantities is unimportant. When gases are involved, as in the case of combustion, the A(pV) term is likely to be significant in magnitude, though still small in comparison with AH or AE. Since it is small, we can employ the perfect-gas law and rewrite Eq. (7) in the form... [Pg.146]

The second section is a somewhat detailed discussion of twenty-two (22) foam properties tested by standard test methods. In most cases only one or a few methods are listed and discussed, but, in the case of combustion properties a total of thirteen (13) methods are considered. This emphasis was made partly because of the considerable attention given to this important subject in recent years. [Pg.354]

Stacks are designed to vent exhaust gases from industrial processes. If the gases are combustible, flare stacks may be used to burn the exhaust gases before they are vented into the atmosphere. In the case of combustible gases, operational procedures should be used that prevent the infiltration of oxygen into the stack where it could mix with the exhaust gases and cause an explosion. Stacks should be built with welded seams rather than bolted joints. Bolted joints, especially joints... [Pg.53]

Materials used in metallic mat technology are Fe-Cr-Al alloys. One of the main worries about using metallic materials is the possibility of oxidation or even corrosive phenomena that may affect the functionality and sometimes even the continuity of the component. When components have to work at high temperatures, as in the case of combustion systems, the kinetics of oxidation and/or corrosion undergo considerable accelerations unless surface phenomena stimulate the formation of... [Pg.507]

The combination of oxygen with other elements is an example of a process chemists call oxidation. In the case of combustion reactions, we say that the fuel is being oxidized and that the oxidation process is something beneficial. In the case of corrosion reactions, metals are being oxidized, as in the case where iron (or steel) combines with oxygen to form rust (ferric oxide, Fe Oj), which is an undesirable process. Most metals are obtained from deposits of their ores where the metal—for example, copper, iron, zinc, aluminum, or lead—occurs in combination with elements such as oxygen, sulfur, or a halogen, or with a combinations of elements as in a silicate, an arsenate, or a carbonate. [Pg.130]

This section presents the governing equations for fluid flow in porous media with precipitation reactions, dissolution of minerals, and laminar premixed combustion, as well as similarity parameters. The model is based on Navier-Stokes equations. For modeling precipitation and dissolution, we used the Boussinesq approximation and Darcy s law, which wiU not be considered in the case of combustion in porous media. Darcy s law, in general, defines the permeability or the ability of a fluid to flow through a porous medium [29]. Another difference from the model of combustion lies in the equations for species, which are based on concentrations. [Pg.110]

The physical effect is related to the formation of a surface barrier layer due to local accumulation of the nanofiller as a consequence of ablation of the polymer. This layer will be rich in the inorganic components of the system, will consequently be thermally stable and will also act to reduce heat transfer into the underlying material. In the case of combustion, its presence will also limit diffusion of degradation products from the polymer to feed the flame. The chemical effect is ascribed to the nanofiller acting to promote the formation of solid rather than gaseous decomposition products (the so-called char), which will then act in the same way as the physical barrier described above. In this latter case, impurity atoms are believed to play an important role (Kashiwagi et al. 2002). [Pg.242]

In the case of combustion reactions, the theory of phlogiston was plausible. When wood bums, it turns into ash. Since the ash clearly weighs less than the wood did, it would seem that something was given off by the wood—phlogiston. [Pg.18]

Such controls may be the replacement of a fine dusty material by a less dusty granular material or reducing the flammable gas to the absolute minimum. Limiting the concentration to avoid the explosive range with mechanical systems linked to ventilation which may be actuated via gas or flow detectors (including alarms) should be considered. In the case of combustible liquids the objective should be to reduce the concentration of any mist formed, below the lower explosion limit, which in turn will ensure it is sufficiently below its flashpoint to prevent explosion. [Pg.131]

TAP is used as a plasticizer in flame-retardant rubber compounds because the other plasticizers provide a fuel source that feeds a fire in the case of combustion. That is why many times this phosphate plasticizer is selected instead of other plasticizers. Recently, the use of triaryl phosphates has attracted attention again because of... [Pg.372]

Table 1. Teaching multiple meanings the case of combustion of methane Macro phase. Table 1. Teaching multiple meanings the case of combustion of methane Macro phase.
In the real world, several reactions usually occur at the same time. In this case, we must write the various reactions as separate, independent reactions. So, for example, in the case of combustion, carbon monoxide can be produced through incomplete combustion of a fuel. In order to describe the production of both CO and CO, we write each reaction separately ... [Pg.142]


See other pages where The Case of Combustion is mentioned: [Pg.191]    [Pg.71]    [Pg.248]    [Pg.130]    [Pg.7]    [Pg.381]    [Pg.5]    [Pg.6]    [Pg.235]    [Pg.248]    [Pg.7]    [Pg.342]    [Pg.96]    [Pg.126]    [Pg.183]    [Pg.546]    [Pg.405]    [Pg.26]    [Pg.928]    [Pg.167]    [Pg.286]    [Pg.158]    [Pg.152]    [Pg.58]   


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