Crude oil is a finite resource found in rocks, the remains of an ancient biomass consisting mainly of plankton that was buried in mud, and is a mixture of a very large number of compounds.
A mixture is defined as two or more elements that are not chemically combined, with the chemical properties of each substance in the mixture unchanged.
It is possible to separate the substances in the mixture by physical methods including distillation.
Most of the compounds in crude oil consist of molecules made up of hydrogen and carbon only (hydrocarbons).
Most of these saturated hydrocarbons are alkanes.
Hydrocarbons have the general formula: C n H 2n+2.
Alkane molecules can be represented in the following forms: MEPB (Monkeys Eat Peanut Butter).
The molecular formula of butane is C4H10.
The first 4 alkanes are methane, ethane, propane and butane.
The oil is heated in the fractionating column and the oil evaporates and condenses at a number of different temperatures.
The many hydrocarbons in crude oil can be separated into fractions each of which contains molecules with a similar number of carbon atoms.
The fractionating column works continuously, heated crude oil is piped in at the bottom.
The vaporised oil evaporates and rises up the column and the various fractions are constantly tapped off at the different levels where they condense.
The fractions can be processed to produce fuels and feedstock for the petrochemical industry.
Many of the fuels on which we depend for our modern lifestyle, such as petrol, diesel oil, kerosene, heavy fuel oil and liquefied petroleum gases, are produced from crude oil.
Many useful materials on which modern life depends are produced by the petrochemical industry, such as solvents, lubricants, polymers, and detergents.
The vast array of natural and synthetic carbon compounds occur due to the ability of carbon atoms to form families of similar compounds.
Alkenes are used for producing other chemicals, such as polymers.
Unsaturated carbons can be represented in the following forms:
The shorter the molecules, the lower the temperature at which that fraction is vaporised or condensed, and the lower its boiling point.
The shorter the molecules, the more flammable it is, making it a better fuel.
The processes for cracking hydrocarbons include passing them over a hot catalyst (catalytic cracking) and mixing them with steam and heated to a very high temperature so that thermal decomposition reactions can occur (steam cracking).
The first two alkenes are ethene and propene.
The longer the molecules, the more viscous it is, making it harder to pour.
If you had to add the other product to this reaction equation: C 6 H 14 → C 2 H 4 + ?, you simply calculate how many carbons and hydrogens are left over.
Hydrocarbons can be cracked to produce smaller, more useful molecules, a process that involves heating the hydrocarbons to vaporise them.
In cracking reactions, you must make sure there are the same number of carbons and hydrogens on each side of the equation, and remember you are going from a bigger molecule to usually 2 smaller molecules.
Alkenes react with bromine water, turning it from orange to colourless, alkanes do not, because an alkene’s double bond makes them more reactive than alkanes.
Shorter the molecules, the less viscous it is, making it more runny.
The products of cracking include alkanes and unsaturated hydrocarbons called alkenes, which have the general formula C n H 2n and have at least one double carbon-carbon bond.
Some of the products made from cracking are useful as fuels, since they have shorter chains than the alkanes you started with, making them more flammable so a better fuel.
Hydrocarbons are burnt so that they can be used as fuel, since the reaction produces energy.
Some properties of hydrocarbons depend on the size of their molecules, influencing their use as fuels.