CIE 0620 Chemistry · IGCSE · Topic 11.3

Fuels

CIE 0620 ChemistryIGCSEFree revision notes

Contents: 7 sections

The three fossil fuels

Coal, natural gas and petroleum are the fossil fuels. All three formed from the remains of organisms buried millions of years ago and compressed under heat and pressure, and all three are finite: they are being used far faster than they form.

Natural gas is mostly methane, CH₄. It burns completely in a good supply of air:

CH₄ + 2O₂ → CO₂ + 2H₂O

Petroleum, also called crude oil, is a mixture of hydrocarbons. As it comes out of the ground it is useless: a thick dark liquid whose components have boiling points ranging from below room temperature to well over 350 °C.

A hydrocarbon is a compound containing hydrogen and carbon only. Methane, ethane, ethene and butane are hydrocarbons. Ethanol, CH₃CH₂OH, is not, because it also contains oxygen, and neither is ethanoic acid. Questions test that definition by offering a compound with an oxygen atom in it.

Fractional distillation of petroleum

The separation works because the different hydrocarbons have different boiling points, and they have different boiling points because their molecules are different sizes. A larger molecule has stronger attractive forces to its neighbours, so more energy is needed to pull it into the vapour.

Diagram walkthrough · 2 minUp the fractionating column, fraction by fractionCognitoFollows the vapour up a column that is hot at the bottom and cool at the top, and explains each fraction leaving as the point where the temperature falls below its boiling point. Longest chains and highest boiling points come off first as bitumen, shortest stay gaseous as refinery gas.

The industrial process:

  1. Crude oil is heated in a furnace to roughly 350 °C, so most of it vaporises.
  2. The hot vapour is fed into the bottom of a tall fractionating column.
  3. The column is hot at the bottom and cooler towards the top, a gradient from about 350 °C to about 25 °C.
  4. The vapours rise. Each hydrocarbon condenses when it reaches a tray whose temperature is below its own boiling point.
  5. Long molecules have high boiling points, so they condense low down. Short molecules stay as vapour longer and condense high up. The shortest of all leave the top still as gases.
  6. The liquid collected at each tray is a fraction, drawn off through a side pipe.

A fraction is still a mixture, not a pure compound. It contains molecules within a narrow range of chain lengths, collected over a range of boiling points, which is why a fraction has no single sharp boiling point.

The fractions and their uses

FractionApproximate carbon atomsUse
Refinery gas1 to 4Heating and cooking
Gasoline (petrol)5 to 10Fuel in cars
Naphtha8 to 12Chemical feedstock for making other compounds
Kerosene (paraffin)10 to 16Jet fuel
Diesel oil (gas oil)14 to 20Fuel in diesel engines
Fuel oil20 to 30Fuel in ships, and home heating systems
Lubricating oil30 to 40Lubricants, waxes and polishes
Bitumenmore than 70Making roads

Learn the list in order, top of the column to bottom. The order is the exam question as often as any individual use is, because a fraction's position tells you its chain length and its chain length tells you its properties.

Naphtha is the odd one out: it is not burnt. It is the feedstock from which plastics, detergents, dyes and medicines are made.

Going down the column, so towards longer chains:

PropertyChange going down
Number of carbon atoms per moleculeIncreases
Boiling pointIncreases
ViscosityIncreases, so the liquid is thicker and flows less easily
ColourDarkens
VolatilityDecreases
Ease of ignitionDecreases, so it is harder to set alight

Every one of these follows from molecular size. Bigger molecules attract each other more strongly, so more energy is needed to separate them: hence a higher boiling point, lower volatility and higher viscosity.

The practical consequence is worth stating. Refinery gas ignites from a spark and burns with a clean flame. Bitumen has to be heated to a few hundred degrees before it will flow at all, and it never burns cleanly, which is exactly why one is piped into a kitchen and the other is spread on a road.

Note carefully that ease of ignition and boiling point move in opposite directions. Petrol has a low boiling point and catches fire easily; fuel oil has a high boiling point and is hard to light. A question asking which fraction ignites most easily wants the one nearest the top.

Supply and demand

Crude oil does not come out of the ground in the proportions the world wants. The short-chain fractions, petrol and naphtha, are in heavy demand and are a small part of the barrel; the long-chain fractions, fuel oil and bitumen, are a large part and are wanted much less.

The industry closes that gap by cracking, which breaks long-chain alkanes into shorter alkanes plus alkenes. That is the subject of 11.5, and the surplus of heavy fractions is the commercial reason it exists.

Common mistakes

Check you have it

Question 1

The pie chart represents the composition of natural gas. Which sector represents methane? Use the source image for M21 Paper 12, question 35.

Diagram from the Cambridge Chemistry 0620 Paper 1 February/March 2021 paper, variant 2, question 35.

Question 2

The pie chart represents the composition of natural gas. Which sector represents methane? Use the source image for M21 Paper 22, question 35.

Diagram from the Cambridge Chemistry 0620 Paper 2 February/March 2021 paper, variant 2, question 35.

Question 3

Fuel oil and naphtha are two fractions obtained from petroleum. What are the major uses of these fractions? Each answer gives, in order: fuel oil; naphtha.

Table from the Cambridge Chemistry 0620 Paper 1 October/November 2022 paper, variant 1, question 35.
What the syllabus asks for on this topicSyllabus points

Syllabus points

  • Name the fossil fuels: coal, natural gas and petroleum.
  • Name methane as the main constituent of natural gas.
  • State that hydrocarbons are compounds that contain hydrogen and carbon only.
  • Describe petroleum as a mixture of hydrocarbons, and describe its separation into useful fractions by fractional distillation.
  • Describe how the properties of the molecules within a fraction change down the column.
  • Name the uses of each fraction.

All of this subtopic is Core, so Extended candidates are examined on it too.

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