Cracking hydrocarbons
What
is cracking?
Cracking
is the name given to breaking up large hydrocarbon molecules into
smaller and more useful bits. This is achieved by using high
pressures and temperatures without a catalyst, or lower temperatures
and pressures in the presence of a catalyst.
The
source of the large hydrocarbon molecules is often the naphtha
fraction or the gas oil fraction from the fractional distillation of
crude oil (petroleum). These fractions are obtained from the
distillation process as liquids, but are re-vaporised before
cracking.
There
isn't any single unique reaction happening in the cracker. The
hydrocarbon molecules are broken up in a fairly random way to produce
mixtures of smaller hydrocarbons, some of which have carbon-carbon
double bonds. One possible reaction involving the hydrocarbon C15H32
might be:

This
is only one way in which this particular molecule might break up. The
ethene and propene are important materials for making plastics or
producing other organic chemicals. The octane is one of the molecules
found in petrol.
Catalytic
cracking
Modern
cracking uses zeolites as the
catalyst. These are
complex aluminosilicates, and are large lattices of aluminium,
silicon and oxygen atoms carrying a negative charge. They are, of
course, associated with positive ions such as sodium ions. You may
have come across a zeolite if you know about ion exchange resins used
in water softeners.
The
alkane is brought into contact with the catalyst at a temperature of
about 500°C and moderately low pressures.
The
zeolites used in catalytic cracking are chosen to give high
percentages of hydrocarbons with between 5 and 10 carbon atoms -
particularly useful for petrol. It also produces high proportions of
branched alkanes and aromatic hydrocarbons like benzene.
Thermal
cracking
In
thermal cracking, high temperatures (typically in the range of
450°C
to 750°C) and pressures (up to about 70 atmospheres) are used
to
break the large hydrocarbons into smaller ones. Thermal cracking
gives mixtures of products containing high proportions of
hydrocarbons with double bonds – alkenes.
Thermal
cracking doesn't go via ionic intermediates like catalytic cracking.
Instead, carbon-carbon bonds are broken so that each carbon atom ends
up with a single electron. In other words, free radicals are formed.
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