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Oxidative combustion

Free radicals are molecular fragments having one or more unpaired electrons, usually short-lived (milhseconds) and highly reaclive. They are detectable spectroscopically and some have been isolated. They occur as initiators and intermediates in such basic phenomena as oxidation, combustion, photolysis, and polvmerization. The rate equation of a process in which they are involved is developed on the postulate that each free radical is at equihbrium or its net rate of formation is zero. Several examples of free radical and catalytic mechanisms will be cited, aU possessing nonintegral power law or hyperbohc rate equations. [Pg.690]

The thermodynamic data for the oxidation (combustion) of the normal and iso-paraffins (alkanes), C2H2 +2, can be represented to within a few kilojoules by the equation... [Pg.57]

Rotary kiln systems usually have a secondary combustion chamber after the kiln to ensure complete combustion of the wastes. Airtight seals close off the high end of the kiln while the lower end is connected to the secondary combustion chamber or mixing cluimber. In some cases, liquid waste is injected into the secondary combustion chamber. The kiln acts as the primary chamber to volatilize and oxidize combustibles in the wastes. Inert ash is then removed from the lower end of the kiln. The volatilized combustibles exit the kiln and enter the secondary chamber where additional oxygen is available and ignitable liquid wastes or fuel can be introduced. Complete combustion of the waste and fuel occurs in the secondar> chamber. [Pg.154]

The strength of the London forces between alkane molecules increases as the molar mass of the molecules increases hydrocarbons with unbranched chains pack together more closely than their branched isomers. Alkanes are not very reactive. but they do undergo oxidation (combustion) and substitution reactions. [Pg.857]

Iron (II) oxide and especially that made by reducing the other oxides, combusts spontaneously if it is heated to 200°C. It also strongly catalyses the combustion of carbon in air. This behaviour can explain the spontaneous inflammable property of the products of burning iron oxalate, which contain this oxide and carbon. When they are placed on the hand and thrown into the air, they form very spectacular showers of sparks. It combusts in contact with liquid oxygen in the presence of carbon. [Pg.204]

The fields of combustion and atmospheric chemistry are intimately connected. Both of these fields are dominated by the reactivity of radical intermediates. The oxidation (combustion) of fossil fuels and their derivatives converts chemical energy into heat... [Pg.247]

Principles and Characteristics Combustion analysis is used primarily to determine C, H, N, O, S, P, and halogens in a variety of organic and inorganic materials (gas, liquid or solid) at trace to per cent level, e.g. for the determination of organic-bound halogens in epoxy moulding resins, halogenated hydrocarbons, brominated resins, phosphorous in flame-retardant materials, etc. Sample quantities are dependent upon the concentration level of the analyte. A precise assay can usually be obtained with a few mg of material. Combustions are performed under controlled conditions, usually in the presence of catalysts. Oxidative combustions are most common. The element of interest is converted into a reaction product, which is then determined by techniques such as GC, IC, ion-selective electrode, titrime-try, or colorimetric measurement. Various combustion techniques are commonly used. [Pg.595]

Second stage ignition during oxidation/combustion of iodomethane in oxygen at 300-500°C was particularly violent, occasionally causing fracture of the apparatus, and was attributed to formation and decomposition of a periodic species. [Pg.179]

The oxidation (combustion) of hydrogen in the air or other oxidant (e.g., pure oxygen) can be subsonic (deflagration) or supersonic (detonation) depending on the strength of the... [Pg.548]

In all of the test methods, the observed burning rates or times are compared to the burning rates or times of reference substances under the same experimental conditions. Based on the comparison with several oxidizing substances having a known classification, the hazard of the sample substance is rated. It should be emphasized that some oxidizer/combustible mixtures will react vigorously. Some mixtures are able to detonate, depending on the specific composition (see Section 2.2.4.2). [Pg.88]

Nitrogen oxides combustion appliances cooking ETS. irritation of respiratory system and eyes decreased in pulmonary function in asthmatics decreased immune capacily, changes in anatomy and function of lung. [Pg.368]

Hydrogen Burner Technology (HBT) (28) was founded to bring to market reformer systems based on the principles of under-oxidized combustion (E OB ). These systems use either non-catalyzed partial oxidation reformers or catalyzed autothermal reformers. The systems for fuel cell applications include all of the components required to deliver anode-ready gas and to... [Pg.222]

Superadiabatic partial oxidation (combustion) process is the thermal decomposition of HjS in HjS-rich waste streams to high-purity hydrogen and elemental sulfur (Slimane et al., 2002). In the superadiabatic combustion (SAC) process, some part of the HjS is combusted to provide the thermal energy required for the decomposition reaction, as indicated by the following two reactions ... [Pg.130]

Nitrogen is nontoxic, but it is an asphyxiate gas that cannot, by itself, support oxidation (combustion) or support life. If you breathe pure nitrogen for any period of time, you will die— not because the nitrogen gas is a poison, but because your body will be deprived of oxygen. [Pg.212]

Fire is a chemical reaction involving rapid oxidation (combustion) of a fuel. [Pg.393]

The determination of total nitrogen by oxidative combustion with chemiluminescence detection is based on the following reactions ... [Pg.184]

A second pyroreactor has been added to the system as back-up, to minimize the system down-time due to furnace heating element failure. The system has been expanded to also perform sulphur determination by oxidative combustion with UV fluorescence detection. The current sample load for the system is greater than 12 000 samples per year with a maximum capacity of the system, operating under optimum conditions, of greater than 40 000 samples per year. [Pg.186]

The size distribution for the large diameter fraction of the H2O oxidizer combustion products is shown in Fig. 8.8, along with the size distribution of the aluminum powder fuel. The mean particle size of the unburned fuel fraction in the combustion products is about 10.7 pm, while the mean size of the fuel particles is 17.4 pm. Most sources report that burning aluminum particles follow a rate law of the form d = do" — Pt, where / is a constant and the exponent n is between 1.5 and 2.0. In that case, the size distribution of the unburned fraction of the combustion products would be expected to be larger than that of the fuel. A size distribution of unburned aluminum smaller than that of the parent fuel is more consistent with particles that never ignited, since the larger particles would probably be undersampled. On the other hand, it seems unlikely that any particle could... [Pg.135]

Bui-Pham, M., K. Seshadri, and F. A. Williams. 1992. The asymptotic structure of premixed methane-air flames with slow CO oxidation. Combustion Flame 89 343-62. [Pg.423]

Typical materials containing oxygen and nitrogen atoms are nitrate esters, such as nitrocellulose (NC) and nitroglycerin (NG). Nitrate esters contain -O-NO2 chemical bonds in their structures. The oxidizer component is represented by the oxygen atoms and the fuel components are the carbon and hydrogen atoms. The oxidized combustion products are COj and HjO, the AHjp values of which are -8.94 MJ... [Pg.35]

The evolution of chemical engineering from petroleum refining, through petrochemicals and polymers, to new applications is de.scribed so that students can see the relationships between past, present, and future technologies. Applications such as catalytic processes, environmental modeling, biological reactions, reactions involving solids, oxidation, combustion, safety, polymerization, and multiphase reactors are also described. [Pg.537]

N-oxides (Misono et al 2001). Substitutions change the Cu s formal oxidation number or state. It is believed that oxygen from N-oxides is adsorbed on the copper surface followed by an electron transfer. However, the mechanism for nitrogen oxide combustion on these oxides is not fully understood. [Pg.210]

Biagini, E., Tognotti, L., Malloggi, S. Pasini, S. 2002. Co-combustion of coal and tire residue in a pilot plant a simplified modelling approach for scale-up predictions of char oxidation. Combustion Science and Technology, 174, 129-150. [Pg.496]

Oxy Oxidizing material any solid or liquid that readily yields oxygen or other oxidizing gas, or that readily reacts to oxidize combustible materials. [Pg.9]

Lauroyl Peroxide — Fire Hazards Flash Point (deg. F) Not pertinent (oxidizing combustible... [Pg.387]

The oxidation process is carried out in the temperature range 300— 450°C, and generally studied at atmospheric pressure. Excess air is usually applied (with some exceptions) and substantial amounts of water vapour may be added to the feed. High initial selectivities (>95%) are feasible, and, although some further oxidation (combustion) of the product is unavoidable, yields of 70—90% are reported in the patent literature. The main by-products are carbon oxides, in addition to minor amounts of acrylic acid, acetaldehyde and formaldehyde. Acrylic acid may be a main product depending on specific catalyst properties and reaction conditions, as described in more detail in Sect. 2.2.3. [Pg.137]

The main products of partial oxidation are aromatic aldehydes and acids formed by oxidation of the reactive methyl group. However, the yields that can be obtained are rather poor, in contrast to the catalytic liquid phase oxidation, which is much more selective. The poor yields are due partly to further oxidation (combustion) of the primary products, and partly to direct oxidation of the aromatic nucleus (also mainly combustion). [Pg.204]

A.B. Bendtsen, P. Glarborg, and K. Dam-Johansen. Low Temperature Oxidation of Methane The Influence of Nitrogen Oxides. Combust. Sci.Techn., 151 31-72,2000. [Pg.815]

H.J. Curran, P. Gaffuri, W.J. Pitz, and C.K. Westbrook. A Comprehensive Modeling Study of Iso-Octane Oxidation. Combust. Flame, 129 253-280,2002. [Pg.818]


See other pages where Oxidative combustion is mentioned: [Pg.322]    [Pg.459]    [Pg.273]    [Pg.229]    [Pg.693]    [Pg.705]    [Pg.58]    [Pg.11]    [Pg.111]    [Pg.411]    [Pg.595]    [Pg.229]    [Pg.216]    [Pg.317]    [Pg.43]    [Pg.72]   
See also in sourсe #XX -- [ Pg.184 , Pg.185 ]




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