Fossil fuels Crude oil, coal and gas are fossil fuels. They were formed over millions of years, from the remains of dead organisms, coal was formed from.

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Presentation transcript:

Fossil fuels Crude oil, coal and gas are fossil fuels. They were formed over millions of years, from the remains of dead organisms, coal was formed from dead plant material crude oil and gas were formed from dead marine organisms. Fossil fuels are non-renewable. They took a very long time to form and we are using them up faster than they can be renewed. Fossil fuels are also finite resources. They are no longer being made or are being made extremely slowly. Once they have all 

http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/crude_oilrev1.shtml

Environmental problems Oil is carried from oil fields to refineries using ocean-going tankers. If it is spilled, it causes considerable damage to the environment: oil slicks travel across the sea, far from the original spill beaches and wildlife are harmed when they are coated with oil. The oil damages feathers and birds may die. Detergents are often used to help clean up oil slicks, but these in turn may harm wildlife.

http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/crude_oilrev3.shtml

http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/crude_oilrev5.shtml

Hydrocarbons Most of the compounds in crude oil are hydrocarbons. This means they only contain hydrogen and carbon atoms

Alkanes Alkanes only have single covalent bonds

Alkenes Alkenes are hydrocarbons that contain a carbon-carbon double bond. Alkenes are 'unsaturated' - meaning they contain a double bond. The presence of this double bond allows alkenes to react in ways that alkanes cannot. This allows us to distinguish alkenes from alkanes using a simple chemical test

Bromine testing http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/making_polymersrev2.shtml The reaction between bromine and alkenes is an example of a type of reaction called an addition reaction. The bromine is decolourised because a colourless dibromo compound forms. For example: ethene + bromine → dibromoethane C2H4 + Br2 → C2H4Br2

The animation shows polymerisation Monomers and polymers Polymers (plastics) are very large molecules made from many smaller molecules called monomers. Alkenes are able to act as monomers because they contain a double bond. They can join end-to-end in a reaction called addition polymerisation. The polymers they form are called addition polymers. In general: A lot of monomers    →    a polymer molecule ethene  →   polyethene propene → polypropene chloroethene →  polychloroethene (Posh word for PVC) The animation shows polymerisation

http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/making_polymersrev3.shtml

Polymerisation Displayed formulae of polymers During polymerisation, the monomers form repeating units in the polymer chain - like railway carriages being hooked up together. Note how the double bond in the monomer becomes a single bond in the repeating unit, and how the repeating unit has a bond at each end.

Uses of polymers Ethene can polymerise to form polyethene, which is also called polythene e.g. a plastic shopping bag or plastic bottle Styrene can polymerise to form polystyrene e.g. insulation and protective packaging

Disposal Landfill disposed of in landfill sites. This uses up valuable land, and suitable sites often fill up quickly. Incineration (burning) Release a lot of heat energy when burnt. Carbon dioxide is produced, which adds to global warming. Toxic gases are also produced, unless the polymers are incinerated at high temperatures. Recycling Many polymers can be recycled. This reduces disposal problems and the amount of crude oil used. But first the different polymers must be separated from each other. This can be difficult and expensive. Biodegradable polymers Most polymers are not biodegradable. This means microorganisms cannot break them down, so may last for many years in rubbish dumps. However, it is possible to include chemicals that cause the polymer to break down more quickly.

Goretex vs Nylon Nylon has some desirable properties. It does not let ultraviolet light pass through it, and it is: Tough, lightweight & waterproof Nylon does not let water vapour pass through it either. This means nylon waterproof clothing traps sweat, so that after a while the inside of the clothing becomes wet, making it unpleasant to wear. Gore-Tex® has the desirable properties of nylon, but is also 'breathable'. It lets water vapour from sweat pass to the outside, but it stops rain drops from passing to the inside. Clothing made of Gore-Tex® is very useful to hikers and other people who work or play outside. The construction of Gore-Tex® - higher Gore-Tex® contains layers of nylon, PTFE and polyurethane. The PTFE contains a lot of tiny holes called pores Each one is too small for water droplets to pass through, but big enough to let water molecules from sweat go through. Without the nylon, the layers would be too fragile to be useful.

Polymer chains Polymer with no cross-links Many polymers, such as polyethene, contain long molecules that lie side by side. These can uncoil and slide past each other, making the material flexible. Long polymer chains have stronger forces of attraction than shorter ones: they make stronger materials.

Cross-linking Polymer with cross-links Cross-linking is where the polymer chains are chemically joined together in places, by covalent bonds. The polymer molecules cannot slide over each other so easily. This makes materials tougher and less flexible, and they cannot be easily stretched. Cross-linking also gives materials high melting points. Vulcanised rubber has cross-links. Its polymer molecules are cross-linked by sulfur atoms. It is tough but flexible, and used for making tyres.

http://www.bbc.co.uk/schools/gcsebitesize/science/ocr_gateway/carbon_chemistry/clean_airrev2.shtml

Factors that need to be considered in a given use of a fossil fuel Energy value Availability Storage Cost Toxicity Pollution e.g acid rain,greenhouse effect Ease of use

Combustion Fuels are substances that react with oxygen to release useful energy. Most of the energy is released as heat, but light energy is also released. About 21 per cent of the air is oxygen. When a fuel burns in plenty of air, it receives enough oxygen for complete combustion.

Complete combustion In general for complete combustion: hydrocarbon + oxygen → carbon dioxide + water

Incomplete combustion Incomplete combustion occurs when the supply of air or oxygen is poor. Water is still produced, but carbon monoxide and carbon are produced instead of carbon dioxide. In general for incomplete combustion: hydrocarbon + oxygen    →    carbon monoxide + carbon + water

Paints Paints are used to decorate surfaces or protect them from damage. A pigment is a coloured substance used in paint. Paints contain these ingredients: a pigment - gives the paint its colour a binding medium - a liquid polymer that hardens to form a continuous layer when the paint dries a solvent - dissolves the binding medium and makes the paint more fluid. Emulsion paints Emulsion paints are water-based. Their solvent is water and they dry when the water evaporates. Oil paints The pigments in oil paints are dispersed in oil, which may itself be dissolved in a solvent. The solvent evaporates away when the paint dries. This leaves the pigment and oil behind. The oil oxidises to form a hard film. This happens because the oil reacts with oxygen in the air. Colloids Paints are a type of mixture called a colloid. In a colloid, particles of one substance are mixed and dispersed with particles of another substance - but they are not dissolved in it. The components do not separate out because their particles are small enough not to settle at the bottom.

Making Esters Esters occur naturally, but can be made in the laboratory by reacting an alcohol with an organic acid. A little sulfuric acid is needed as a catalyst. This is the general word equation for the reaction: alcohol + organic acid    →    ester + water For example: methanol + butanoic acid    →    methyl butanoate + water The diagram shows how this happens, and where the water comes from:

Cosmetics testing Medicines New medical drugs have to be tested to ensure they work and are safe before they can be prescribed. There are three main stages: The drugs are tested using computer models and human cells grown in the laboratory. Drugs that pass the first stage are tested on animals. A typical test involves giving a known amount of the substance to the animals, then monitoring them carefully for any side-effects. Drugs that have passed animal tests are used in clinical trials. They are tested on healthy volunteers to check they are safe. The substances are then tested on people with the illness that the drugs are designed to treat to ensure that they are safe and work properly.