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Welcome to GCSE Edexcel Science revision.

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Unit S C 24: Polymers.

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A polymer is a substance made from many repeating units linked together, giving a high average relative molecular mass.

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A monomer is a small molecule that can join into a polymer chain.

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In addition polymerisation, monomers containing C double bonded to C add together.

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The double bond opens to form single bonds linking a chain; no small-molecule by-product is lost.

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Ethene forms poly(ethene).

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Draw a repeat unit with a single C to C bond,

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two hydrogens on each carbon,

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continuation bonds crossing brackets,

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and n outside the brackets;

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the bracketed unit is part of a chain,

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not an isolated ethane molecule.

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Continuation bonds cross the brackets; n represents many repeating units.

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Propene forms poly(propene), with a C H 3 side group on alternate backbone carbons.

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Chloroethene forms poly(chloroethene), PVC, with a chlorine side group; tetrafluoroethene forms PTFE, with fluorine atoms replacing the hydrogens.

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To obtain an addition monomer from a repeat unit, identify the two backbone carbons and restore the C double bonded to C bond between them, keeping their side groups.

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To obtain the repeat unit from a monomer, open C double bonded to C and draw chain continuation bonds.

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Polymer molecules have different chain lengths, so their relative molecular masses form a distribution and are described with an average.

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Longer chains and chain interactions can affect material properties.

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Different monomers and processing produce polymers with different properties.

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Polymer does not mean a single material with one melting behaviour or strength.

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Poly(ethene) can be flexible and water-resistant, useful for bags, packaging and bottles; grades differ in stiffness and density.

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Poly(propene) is tough and light, useful for containers, fibres and some reusable hinges.

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Select it from property data rather than assuming all plastics are interchangeable.

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PVC can be rigid for pipes or window frames, or made flexible with plasticisers for cable insulation.

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Its electrical insulation and durability are useful, but disposal requires care.

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PTFE is chemically resistant, slippery and heat-resistant for many uses, including non-stick coatings.

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It is not an excuse to ignore manufacturer temperature limits.

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Compare polymer properties with the demands of a product: flexibility, toughness, density, electrical insulation, chemical resistance, heat resistance and cost.

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A useful property in one setting can be a disadvantage in another.

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(Higher tier) A polyester can form when a molecule with two carboxylic-acid groups reacts with a molecule with two alcohol groups.

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Two functional groups on each monomer allow growth in both directions.

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(Higher tier) A carboxylic-acid group reacts with an alcohol group to form an ester link, releasing a water molecule.

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Repeating this forms a polyester by condensation polymerisation.

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Unlike addition polymerisation, a small molecule is released when each link forms.

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A diacid and a diol can form many ester links along a polyester chain.

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(Higher tier) The ester link contains carbon double bonded to oxygen and single bonded to oxygen.

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Draw both carbonyl and single-bonded oxygens; the water comes from an O H of the acid and a hydrogen from the alcohol group.

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(Higher tier) Each monomer with two functional groups can join at both ends.

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If k such molecules join to make one straight chain with no rings, they form k minus 1 links and release k minus 1 water molecules.

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Repeat-unit drawings show the repeating pattern rather than the chain’s end groups.

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D N A is a natural polymer of nucleotides; four different nucleotide types are used.

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Starch is based on sugar monomers, while proteins are polymers of amino acids.

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Natural and synthetic polymers can have very different biodegradability and properties.

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Being a polymer alone does not establish whether a material will persist in landfill.

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Many conventional synthetic polymers are not readily biodegradable and can persist in landfill or the environment.

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Litter and fragmented plastic can affect wildlife; landfill persistence is separate from toxicity.

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Making polymers often uses finite petrochemical resources.

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Recycling can reduce demand for new feedstock, but collection, sorting, cleaning and processing require energy and money.

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Different polymers must usually be separated before melting and reforming, because mixed materials can produce poor-quality products.

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Contamination and additives can complicate recycling.

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Burning polymers can recover energy but produces carbon dioxide and may release harmful gases depending on composition and conditions;

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chlorine-containing polymers can produce acidic gases.

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Controlled emissions treatment is needed.

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Reuse can avoid repeated manufacture when products are durable and used enough times.

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Compare whole-life data, transport, washing, breakage and disposal rather than assuming reuse always wins for every scenario.

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Choose disposal routes using economic costs, available collection systems, recovered material quality, energy use and environmental effects.

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Recycling rates and theoretical recyclability are different claims.

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That completes Polymers.

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Revisit the notes and test yourself on the revision website.
