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This page describes
what cracking is, and the differences between catalytic cracking and thermal
cracking used in the petrochemical industry.
Cracking
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:
Or, showing more clearly
what happens to the various atoms and bonds:
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 (gasoline).
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 (gasoline). It
also produces high proportions of branched alkanes and aromatic hydrocarbons like
benzene.
For UK A level (and
equivalent) purposes, you aren't expected to know how the catalyst works, but
you may be expected to know that it involves an ionic intermediate.
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Note: You should check your syllabus to find out exactly what you need to know.
If you are studying a UK-based syllabus and haven't got one, follow this
link.
Use the BACK button
on your browser to return quickly to this page.
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The zeolite catalyst
has sites which can remove a hydrogen from an alkane together with the two
electrons which bound it to the carbon. That leaves the carbon atom with a
positive charge. Ions like this are called carbonium ions (or carbocations).
Reorganisation of these leads to the various products of the reaction.
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Note: If you are interested in other examples of catalysis in the
petrochemical industry, you should follow this link. It will lead you to information
on reforming and isomerisation (as well as a repeat of what you have just
read about catalytic cracking).
Use the BACK button
on your browser if you want to return quickly to this page.
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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.
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Warning! This is a gross oversimplification, and is
written to satisfy the needs of one of the UK A level Exam Boards (AQA). In
fact, there are several versions of thermal cracking designed to produce
different mixtures of products. These use completely different sets of
conditions.
If you need to know
about thermal cracking in detail, a Google search on thermal cracking
will throw up lots of useful leads. Be careful to go to industry (or
similarly reliable) sources.
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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.
Reactions of the free
radicals lead to the various products.
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