Crude oil as a source of organic chemicals.

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Hydrocarbon Fuels Project

Crude oil as a source of organic chemicals.

Crude oil accounts for much of the wealth of the industrialised world. Crude oil exploitation has led to fuels for heating, generating electricity and powering motor vehicles. As well as used for fuel, products of crude oil are processed into petrochemicals for use in industry. In the UK the chemical industry provides jobs for 250,000 people. This means that the UK is very dependent upon crude oil and its products. Crude oil is made up of many types of hydrocarbons. There are three main types of hydrocarbon. These are arenes, cycloalkenes and alkanes.

To separate the hydrocarbons in crude oil we use a process called fractional distillation. This process involves heating the crude oil in a fractional distillation column. At different temperatures different fractions evaporate off and then they cool at different levels of the column. Now each fraction contains a small mixture of hydrocarbons, that’s boiling points are fairly similar.

Fractional distillation separates crude oil into these fractions: refinery gas, gasoline, naphtha, kerosine, (gas) diesel, oil and residue. The refinery gases are the simplest alkanes, containing up to four carbons, and are used as sources for other molecules. Gasoline is used as petrol while naphtha is very important in the chemical industry. Kerosine is used for jet fuel in aviation while diesel is used as diesel petrol for transport. The residue is used for lubrication, waxes and for bitumen, which is used in tarmac for roads.

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Cracking, isomerisation and reforming.

Once fractional distillation is complete there is still not enough product from the crude oil to meet the needs of industry. It is for this reason why certain fractions are cracked. Cracking is when an oil fraction is heated with a catalyst. The product of this is a low molecular mass alkane and an alkene. C-C bonds and C-H bonds are both broken randomly so other products like hydrogen may be given out. It is also possible for branched-chain isomers to be formed.

Here is an example:

CH3CH2CH2CH2CH2CH2CH2CH2CH2CH3

(Decane)

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