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Fuels alkanes

Considerable attention has been paid to the application of CNTs as the catalyst support for Fischer Tropsch synthesis (FTS), mainly driven by utilization of the confinement effect (Section 15.2.3). In general, this process is a potential alternative to synthesize fuel (alkanes) or basic chemicals like alkenes or alcohols from syngas, which can be derived from coal or biomass. The broad product spectrum, which can be controlled only to a limited extent by the catalyst, prohibited its industrial realization so far, however, it is considered an important building block for future energy and chemical resource management based on renewables. [Pg.419]

More than 130 different types of alkanes have been identified in the atmosphere [27] and they comprise a major fraction of the organic pollutants found in urban atmospheres (see Table 3). They are released in large amounts in activities connected with the extraction, refining, distribution, and combustion of fossil fuels. Alkanes are also released during the combustion of organic matter and by microbiological processes associated with the decay... [Pg.130]

Examples of Hydrogen Distribution in Fossil-Fuel Alkane Extracts Measured from 100 MHz H N,M,R Spectra ... [Pg.33]

MTBE and Problems Associated with It MTBE and Lead in Gasoline Race Cars and Their Fuel Alkanes and Cycloalkanes Manipulate Common Functional Groups in 3D... [Pg.283]

Alkane properties Alkanes are nonpolar compounds with relatively low melting and boiling points compared to polar molecules of similar mass. Alkanes have low solubilities in water. They also have low reactivities, but they readily undergo combustion in oxygen and are commonly used as fuels. Alkanes are saturated hydrocarbons that contain only single bonds. In the next section, you will examine unsaturated hydrocarbons, which have at least one double or triple bond between carbon atoms. [Pg.226]

Mechanisms related to cellulose-derived biofuels focus on the chemistry offuran derivatives. Beyond the unimolecular decompositions and oxidative reactions discussed previously in this section, furan derivatives can undergo a wide variety of other reactions. They are transformed by pyrolytic, hydrolytic, and other chemical processes to longer chain ethers (R1OR2) and aldols (hydroxyaldehydes and hydroxyketones, Ri(0H)R2C(0)R3). These oxygenated species are then converted through hydrogenation and deoxygenation processes to liquid HC fuels (alkanes). [Pg.161]

Higher octane gasoline typically contains a greater proportion of branched alkanes relative to unbranched ones Are branched alkanes better fuels because they give off more energy on com bustion" Explain... [Pg.102]

Poly(vinyl nitrate) has been prepared and studied for use in explosives and rocket fuel (104,105). Poly(vinyl alcohol) and sulfur trioxide react to produce poly(vinyl sulfate) (106—111). Poly(vinyl alkane sulfonate)s have been prepared from poly(vinyl alcohol) and alkanesulfonyl chlorides (112—114). In the presence of urea, poly(vinyl alcohol) and phosphoms pentoxide (115) or phosphoric acid (116,117) yield poly(vinyl phosphate)s. [Pg.481]

Compounds containing only carbon and hydrogen are termed paraffins or alkanes. The general formula for these compounds is C H2n+2 where n is an integer. When only single bonds are present between carbon atoms they are classified as saturated . Examples include, etliane, propane, and butane the last two are common fuel gases ... [Pg.34]

When the initial sphere consists only of vapor, the value of m, must be taken as zero, and M equals the molecular weight of the fuel. Most models are tested with low-molecular-weight alkanes. [Pg.172]

This will generally be tr-ue as we proceed to look at other alkanes as the number of carbon atoms increases, so does the boiling point. All the alkanes with four car bons or less are gases at room temperature and atmospheric pressure. With the highest boiling point of the three, propane is the easiest one to liquefy. We are all faniliar- with propane tanks. These are steel containers in which a propane-rich mixture of hydrocar bons called liquefied petroleum gas (LEG) is maintained in a liquid state under high pressure as a convenient clean-burning fuel. [Pg.63]

Reaction with oxygen occurs during combustion in an engine or furnace when the alkane is used as a fuel. Carbon dioxide and water are formed as products, and a large amount of heat is released. For example, methane (natural gas) reacts with oxygen according to the equation... [Pg.91]

In addition to the catalyzed reactions used in the refining of petroleum (see Sections 18.5 and 18.9), alkanes undergo two common reactions oxidation and substitution (Section 18.4). The alkanes are commonly used as fuels, because their combustion to carbon dioxide and water is highly exothermic (Section 6.17) ... [Pg.857]

Saturated hydrocarbons are the main constituents of petroleum and natural gas. Mainly used as fuels for energy production they also provide a favorable, inexpensive feedstock for chemical industry [74]. Unfortunately, the inertness of alkanes renders their chemical conversion challenging with respect to selectivity. Clearly, the development of new and improved methods for the selective transformation of alkanes belongs to the central goals of catalysis. Iron-catalyzed processes might be a smart tool for such transformations (for reviews see [75-77]). [Pg.93]

The C-C and C-H BDEs for ethane are 377.0 and 423.0kJ/mol, respectively, and the H-0 BDE of hydroperoxyl (HO2 ) radical is only 207.5kJ/mol. The large reaction endothermicities for reactions 6.4 and 6.5 highlight the unlikeliness of their occurrence at lower temperatnres. In pyrolytic (heat, but no oxidant) or high fuel/oxidant ratio conditions, the endothermicities indicate that ethane and other alkanes will... [Pg.250]

Figure 6.2. Typical ignition delay of an alkane fuel as a function of the initial mixture s temperature. Three different kinetic models are shown (a) High temperature chemistry only that is, no peroxy radical chemistry, (b) Same as (a), but the Q OOH chain-branching channel of the peroxy radicals has been considered, (c) Same as (b), bnt the concerted elimination of RO2 to alkene + HO2 has been considered. (Figure courtesy of Timothy Barckholtz, ExxonMobil Research and Engineering.)... Figure 6.2. Typical ignition delay of an alkane fuel as a function of the initial mixture s temperature. Three different kinetic models are shown (a) High temperature chemistry only that is, no peroxy radical chemistry, (b) Same as (a), but the Q OOH chain-branching channel of the peroxy radicals has been considered, (c) Same as (b), bnt the concerted elimination of RO2 to alkene + HO2 has been considered. (Figure courtesy of Timothy Barckholtz, ExxonMobil Research and Engineering.)...
After radical initiation of an alkane fuel, chain branching is immediately accessible via new high-temperature pathways with O2 ... [Pg.255]


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See also in sourсe #XX -- [ Pg.92 , Pg.94 ]




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