Separates out different hydrocarbons by the length of their carbon chains
Shortest hydrocarbons
Most flammable, make the best fuels
Longer chain hydrocarbons
Thick viscous liquids, comparatively less useful
Cracking
Breaks down longer less useful hydrocarbons into shorter more flammable hydrocarbons
Thermal decomposition
Breaking down molecules by heating them
Cracking methods
Catalytic cracking
Steam cracking
Catalytic cracking
Heat long chain hydrocarbons and vaporize, pass over hot powdered aluminium oxide catalyst which splits apart into two smaller hydrocarbons
Steam cracking
Vaporize hydrocarbons, mix with steam, heat to very high temperature which causes long hydrocarbon chains to split apart into shorter ones
Balanced chemical equation for cracking long chain alkanes
Long chain alkane (e.g. decane) goes to form shorter alkane (e.g. heptane) and alkene (e.g. propene)
Number of carbons and hydrogens on each side of the equation must be the same
Alkenes
More reactive than alkanes
Can be added together to make polymers
Adding bromine water to a solution of alkenes
Decolorizes the bromine water from orange to colorless
Cracking reaction
Decane (C10H22) can be cracked into ethene (C2H4) and another hydrocarbon
Balanced equation for cracking decane
Decane (C10H22) goes to form ethene (C2H4) and another hydrocarbon (C8H18)
Crude oil
A fossil fuel that we get from deep under the ground, a mixture of lots of different compounds
Crude oil
Nearly all of the compounds are hydrocarbons which contain only hydrogen and carbon
The most common type of hydrocarbons are alkanes
Formation of crude oil
1. Remains of dead plants and animals, particularly plankton, buried in the mud
2. High pressures and temperatures under the ground turned this organic biomass into crude oil
3. Crude oil soaked into the rocks and was stored for millions of years
Crude oil is a finite resource
Fractional distillation
A process used to separate the different hydrocarbons in crude oil by making use of their different boiling points
Fractional distillation
1. Feed the oil into a chamber and heat it until most of it has turned into a gas
2. Pass the gaseous mixture into a fractionating column which is hot at the bottom but gets cooler towards the top
3. Hydrocarbons with the longest chains condense first and drain out early
4. Shorter chain hydrocarbons stay gaseous longer and condense higher up the column
Fractions obtained from fractional distillation
Bitumen
Heavy fuel oil
Diesel
Petrol
Kerosene
LPG (propane and butane)
Fractions from fractional distillation
Shorter chain hydrocarbons are more flammable and make better fuels
Longer chain hydrocarbons are often poor fuels and can be broken down further by cracking
Petrochemicals
Substances obtained from crude oil that can be used as feedstock (raw materials) for the petrochemical industry to make things like solvents, lubricants, polymers and detergents
Alkanes
A homologous series of hydrocarbons that contain only carbons and hydrogen atoms with no double bonds
We covered the names of the first four alkanes in the series in this video
Alkanes
As the length of the carbon chain increases:
Boiling point increases
Shorter alkanes are more volatile and evaporate more easily
Longer alkanes are more viscous and thick
Shorter alkanes are more flammable and easier to ignite or burn
Combustion reactions
1. Hydrocarbon reacts with oxygen
2. Forms carbon dioxide and water
3. Releases energy (exothermic)
Complete combustion
Hydrocarbon reacts with enough oxygen to form carbon dioxide and water
Writing balanced combustion equations
1. Write unbalanced equation
2. Balance carbon atoms
3. Balance hydrogen atoms
4. Balance oxygen atoms
Hydrocarbons like alkanes are used as fuels because they release energy when combusted