Addition Polymers
In addition polymerisation, many alkene monomers open their C=C π bonds and join into a long saturated chain; no other product forms. The repeat unit is drawn by turning C=C into C–C with extension bonds through brackets: ethene → poly(ethene), chloroethene → poly(chloroethene) (PVC), propene → poly(propene). Poly(alkenes) are unreactive (saturated, non-polar C–C and C–H bonds), so they're non-biodegradable. Disposal: landfill (lasts centuries), incineration (energy recovery but CO₂ and, for PVC, HCl and dioxins), recycling, or biodegradable alternatives.
Learning objectives
- Draw repeat units from monomers and vice versa.
- Explain why poly(alkenes) are unreactive.
- Evaluate methods of disposal.
Poly(ethene) is an alkane, not an alkene. Why?
Core idea
A poly(ethene) bag can last hundreds of years in landfill. The same chemistry that makes it useful makes it a problem.
Alkene monomers open their C=C bonds and link into saturated chains. The product is as unreactive as an alkane, so it barely degrades.
1. Repeat units
- Draw the two C=C carbons with all substituents.
- Change C=C to C–C and add a bond on each side.
- Brackets with extension bonds passing through them; add .
A PVC chain has . How many chloroethene units ( 62.5) does it contain?
- Goal
- .
- Strategy
- Divide polymer mass by monomer mass.
- Monomer mass.
- No by-product, so masses add.
Each option has a cost.
Summary
- No by-product.
- Repeat unit has two main-chain carbons.
- Inert, non-biodegradable.
- Monomer
- Small molecule that joins to form a polymer.
- Repeat unit
- Smallest section that repeats along the chain.
- Biodegradable
- Broken down by microorganisms.
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