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INTRODUCTION
Fuel is a substance which, when burnt, i.e. on coming in contact and
reacting with
oxygen or air, produces heat. Thus, the substances classified as fuel must
necessarily
contain one or several of the combustible elements : carbon, hydrogen,
sulphur, etc. In
the process of combustion, the chemical energy of fuel is converted into
heat energy.
To utilize the energy of fuel in most usable form, it is required to transform
the fuel from
its one state to another, i.e. from solid to liquid or gaseous state, liquid to
gaseous state,
or from its chemical energy to some other form of energy via single or
many stages. In
this way, the energy of fuels can be utilized more effectively and
efficiently for various
purposes.
Objectives
After studying this unit, you should be able to
Advantages
(a)
(b)
They are convenient to store without any risk of spontaneous
explosion.
(c)
(d)
Disadvantages
(a)
(b)
(c)
(d)
(e)
Types of coals:
Analysis of Coal
The importance of volatile matter in coal is due to the fact that it largely
governs the combustion which in turn governs the design of grate and
combustions space used. High volatile matter is desirable in gas making,
while low volatile matter for manufacturing of metallurgical coke.
anthracites all require the use of a binder, such as pitch, for the
production of satisfactory briquettes. The briquetting of brown coals
without binder has been developed extensively in Germany and in
Victoria, Australia. In these places large-scale plants have been in
operation for some years to upgrade the brown coal deposits.
b- Carbonized Briquettes (Lurgi Process)
It has been found in Germany that many types of lignite, although
not forming cokes
on carbonization at ordinary rates in coke-ovens or gas retorts, will
form strong, coherent, residues if carbonized rapidly. Lignites that do
not form a coherent residue on carbonization can usually be made to
form a serviceable coke if carbonized after
briquetting.
4- Processes of Manufacture
Coal Pyrolysis
Pyrolysis of coal dates back to the eighteenth century, using
temperatures below 700 C (1290 F) in fixed- or moving fixed-bed
reactors. The primary product was a low-volatile smokeless domestic
solid fuel, although the value of the liquid products was also soon
recognized. During the 1920s and 1930s there was a great deal of
R&D in low-temperature processes, but interest dwindled in the mid1940s when gas and oil became readily available at low prices. With
the oil embargo and increased oil prices of the early 1970s, interest
renewed in coal pyrolysis, but in more recent times interest has
again declined along withmpetroleum prices (Khan and Kurata,
1985).
Pyrolysis kinetics are reasonably well understood and have been
modelled extensively (Solomon et al., 1993). Both yield and liquid
fuel properties depend on pyrolysis conditions. Pyrolysis under mild
temperatures (500 C to 700 C [930 F to 1290 F]) and pressures
(up to 50 psig) with rapid heat-up can produce high liquid yields
without adding hydrogen. However, a significant part of the feed
coal remains as char with market value comparable to or somewhat
less than that of the feed coal. Coal pyrolysis offers some promise of
lower liquid costs if the char can be upgraded to higher-value
specialty products, such as form coke, smokeless fuel, activated
carbon, or electrode carbon, or if the liquid yield can be significantly
increased by using low-cost reactants (steam and carbon dioxide) or
catalysts. Pyrolysis liquids have a low hydrogen-to-carbon ratio,
generally less than one, in contrast to petroleum tars and bitumen
(around 1.4) and high-quality petroleum products (approximately
2.0). They also contain substantial amounts of oxygen, compared to
tars, and thus require more extensive hydrogen addition to produce
specification fuels. Their tendency to polymerize on standing can
cause operational problems, which also must be addressed. Little
heat is required to produce pyrolysis liquids from coal, however, and
production as a side stream to coal gasification or fluidized-bed
combustion is efficient.