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Condensation Polymerisation

Dominic Weston Chemistry A2 English

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Condensation Polymerisation

  1. Disposing of Polymers

    • Polyalkenes (addition polymers) have non polar carbon bonds
      • Makes them unreactive and chemically inert - non-biodegradable
        • Condensation polymers have polar c-c bonds - open to attack from nucleophiles
          • these polymers broken down by hydrolysis making them biodegradable (very slow process)
            • Dispose of polymers by Burying, Burning or Recycling
              • Burying
                • Landfill if plastics cannot be seperated from other waste or not economically viable
                  • Landfill is cheap and easy method
                    • Decomposes to release methane a greenhouse gas
                      • Limited amount of space
              • Burning
                • Heat used to generate electricity
                  • Heavily controlled process to reduce toxic gases
                    • E.g. HCl reacts with a base while passed through scrubbers
                      • Gases can still contribute to greenhouse effect
              • Sorting and recylcing
                • Some plastics can be melted and remoulded
                  • Some can be cracked into monomers to be used
                    • Advantages
                      • Reduces landfill waste
                        • Saves raw materials
                          • Recycling costs less than making new plastic
                            • Produces less CO2 than burning
                    • Disadvantages
                      • Technically difficult to recycle
                        • Collecting, sorting and processing expensive than landfill/burn
                          • Can't often remake the same plastic
                            • Plastic can be contaminated while recycling
  2. Condensation Polymers

    • Monomers join together forming a link and removing water
      • Includes polyamides, polyesters, polypeptides
        • Polyamides formed from dicarboxylic acid and diamines
          • 2n Water removed, amide link between carboxyl and amino group
            • E.g. Nylon 6,6; Kevlar
        • Polyesters made from Dicarboxylic acids and diols
          • 2n Water removed, ester link between carboxyl and hydroxyl groups
            • E.g. Terylene
        • Hydrolysis produces original monomers
          • Water molecules added and links broken
            • Two seperate monomers with their groups and end of molecules finished
        • Where n = any large number
    • These polymers are stronger and more rigid than addition polymers
      • Addition polymers - polyethene
      • These Conc polymers contain have polar bonds
        • Causes VDW, perm dipole-dipole, hydrogen bonds all cause strength

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A2 Chemistry (Organic 2) Mind Map on Condensation Polymerisation, created by Dominic Weston on 19/03/2018.
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