Degradability of Polymers (Cambridge (CIE) A Level Chemistry): Revision Note
Poly(alkenes) & Biodegradability
Many of the polymers in use have been produced through addition polymerisation of alkenes
The (poly)alkene chains are non-polar and saturated
This makes them chemically inert and, therefore, non-biodegradable
(Poly)alkenes can be melted and recycled for new uses
However, even in the new applications, the (poly)alkenes are not biodegradable
Recycling plants can burn used plastic materials
The energy released from burning can be used to generate electricity
Burning plastics in oxygen releases carbon dioxide and water (complete combustion) which can contribute to global warming
Photodegradation of Polymers
Polyesters and polyamides are biodegradable polymers for a number of reasons
One such reason is their ability to breakdown with the use of light
Carbonyl groups (C=O) along polymer chains are able to absorb energy from the Electromagnetic Spectrum, in particular ultraviolet (UV) light
Absorbing UV light weakens the carbonyl areas of polymers and breaks them down into smaller molecules
Disadvantages of photodegradability
Despite this ability being a great advantage of polyesters and polyamides, it may pose problems when the polymers are repurposed
When applied to a new use, the biodegradability could give a weaker polymer
Breaking down polymers also poses another challenge
Once used, polymeric materials are taken to landfill sites where many other materials are piled on top of each other
This could mean that photodegradable polyesters or polyamides do not have access to UV light in order to break down naturally
Biodegrading Polyesters & Polyamides
Biodegradable polymers
Both polyesters and polyamides can be broken down using hydrolysis reactions
This is a major advantage over the polymers produced using alkene monomers (polyalkenes)
When polyesters and polyamides are taken to landfill sites, they can be broken down easily and their products used for other applications
Hydrolysis of polyamides
Hydrolysis is the breakdown of molecules using water
In acidic hydrolysis, an acid (such as hydrochloric acid) acts as the catalyst
Polyamides such as Kevlar are heated with dilute acid
This reaction breaks the polyamide into a dicarboxylic acid and ammonium ions
Alkaline hydrolysis
The polyamide is heated with a species containing hydroxide ions (eg. sodium hydroxide)
This breaks the polymer into the sodium salts of its monomers (dicarboxylic acid salt and diamines)
Hydrolysis of Kevlar, a polyamide
Hydrolysis of Kevlar produces different products based on whether it is acid hydrolysis or base hydrolysis
Hydrolysis of polyesters
Ester linkages can also be degraded through hydrolysis reactions
The acidic and alkaline hydrolysis of polyethylene terephthalate (PET) is shown
Hydrolysis of polyethylene terephthalate (PET), a polyester
Hydrolysis of polyethylene terephthalate (PET) produces different products based on whether it is acid hydrolysis or base hydrolysis
Acid hydrolysis forms the diol and dicarboxylic acid that were used to form the polyesters
Alkaline hydrolysis forms the diol and dicarboxylic acid salt
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