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*Revision Materials* 1 Atomic Structure 2 Atoms, molecules and stoichiometry 3 Chemical Bonding 4 States of matter 5 Chemical energetics 6 Electrochemistry 7 Equilibria 8 Reaction kinetics 9 The Periodic Table, chemical periodicity 10 Group 2 11 Group 17 12 Nitrogen and sulfur 13 Organic 14 Hydrocarbons 15 Halogen compounds 16 Hydroxy compounds 17 Carbonyl compounds 18 Carboxylic acids and derivatives 19 Nitrogen compounds 20 Polymerisation 21 Organic synthesis 22 Analytical techniques 23 Chemical energetics 24 Electrochemistry 25 Equilibria 26 Reaction kinetics 27 Group 2 28 Chemistry of transition elements 29 Organic 30 Hydrocarbons 31 Halogen compounds 32 Hydroxy compounds 33 Carboxylic acids and derivatives 34 Nitrogen compounds 35 Polymerisation 36 Organic synthesis 37 Analytical techniques

35 Polymerisation

35.1 Condensation polymerisation 35.2 Predicting the type of polymerisation 35.3 Degradable polymers

Degradable Polymers

Specification Reference Organic Chemistry, Polymerisation 35.3

Quick Notes

  • Polyalkenes (e.g. poly(ethene), poly(propene)) are chemically inert and non-biodegradable.
  • Some polymers contain additives that enable degradation by light (photodegradable).
  • Polyesters and polyamides can biodegrade via hydrolysis in acidic or alkaline conditions.
  • Biodegradable polymers break down more easily in the environment, helping reduce pollution.

Full Notes

Poly(alkenes) and Biodegradability

Poly(alkenes), such as poly(ethene) and poly(propene), are made by addition polymerisation of alkenes.

These polymers have only strong C–C and C–H bonds, with no polar or reactive functional groups.

CIE A-Level Chemistry diagram showing the structure of poly(alkenes) like poly(ethene) with strong C–C and C–H bonds, explaining why they are chemically inert and non-biodegradable.

As a result, they are:

Photodegradable Polymers

Some synthetic polymers are made to be photodegradable, meaning they break down under UV light or sunlight.

CIE A-Level Chemistry diagram showing how photodegradable polymers break down when exposed to UV light or sunlight.

This is achieved by adding light-sensitive groups to the polymer chain or incorporating metal-based additives that catalyse degradation when exposed to light.

A possible limitation is that photodegradation only occurs in environments with sufficient light exposure meaning it isn't effective in buried landfills.

Biodegradable Condensation Polymers

Unlike poly(alkenes), polyesters and polyamides contain functional groups (–COO– and –CONH–) that are susceptible to hydrolysis.

CIE A-Level Chemistry diagram showing hydrolysis of polymers with ester and amide functional groups.

These polymers can be broken down:

Polyesters (e.g. PLA – polylactic acid) and polyamides (e.g. nylon, proteins) are therefore biodegradable and suitable for eco-friendly uses.

For Example
Polyesters can be broken down into diocarboxylic acids and diols.

CIE A-Level Chemistry diagram showing hydrolysis of polyesters breaking down into diols and dicarboxylic acids.

Summary

Polymer Type Key Bonds Biodegradability Degradation Method
Poly(alkenes) C–C, C–H Non-biodegradable Very resistant, only photodegradable with additives
Polyesters Ester (–COO–) Biodegradable Hydrolysis (acid/alkali), microorganisms
Polyamides Amide (–CONH–) Biodegradable Hydrolysis (acid/alkali), enzymes