polymers Flashcards

1
Q

What is addition polymerisation?

A

Long chain molecules made from joining together many shorter molecules (monomers) with nothing else produced.

Examples include poly(ethene), PVC, and poly(propene)

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2
Q

What is condensation polymerisation?

A

Long chain molecules made from joining together many shorter molecules (monomers) with some small molecule also formed (e.g. water).

Examples include polyesters (e.g. terylene) and polyamides (e.g. nylon, Kevlar)

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3
Q

What are the monomers involved in addition polymerisation?

A

Alkenes, which are molecules with C=C bonds.

Alkenes serve as the building blocks for addition polymers.

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4
Q

What are the monomers involved in condensation polymerisation?

A

Usually 2 different monomers with 2 different functional groups:
* Dicarboxylic acids with diols (polyesters)
* Dicarboxylic acids with diamines (polyamides)
* Amino acids (polyamides/polypeptides)

These combinations lead to the formation of polymers like nylon and terylene.

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5
Q

What is the reaction for forming a polyester?

A

Dicarboxylic acid + diol → polyester. Water is released and an ester link is formed.

This process illustrates the condensation polymerisation mechanism.

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6
Q

What is the reaction for forming a polyamide?

A

Dicarboxylic acid + diamine → polyamide. Water is released and an amide link is formed.

This reaction is key in the formation of materials like nylon and Kevlar.

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7
Q

What is the formation of polyamides from amino acids?

A

Amino acid + amino acid → polyamide. Water is released and an amide (peptide) link is formed.

This process is essential in forming proteins.

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8
Q

What are the uses of nylon?

A

Used in clothing due to its strong, flexible, and stretchy fibres.

Nylon is widely adopted in textile applications.

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9
Q

What are the characteristics of Kevlar?

A

Strength is due to rigid chains and flat aromatic rings that pack together, held by strong intermolecular forces.

Kevlar is used in bulletproof vests and anti-stab clothing.

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10
Q

Are polyalkenes biodegradable?

A

No, polyalkenes are not biodegradable.

They are long-chain alkane molecules that are inert.

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11
Q

How are polyalkenes typically disposed of?

A

Disposed of in landfill sites, incineration, or some may be melted down and remoulded.

The disposal methods reflect their non-biodegradable nature.

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12
Q

Are condensation polymers potentially biodegradable?

A

Yes, they are potentially biodegradable if broken down by hydrolysis.

Hydrolysis reverses the polymerisation process and can break down polar bonds.

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13
Q

What is the advantage of recycling polymers?

A

Saves using crude oil, which is expensive and diminishing, and uses less energy in refining.

Recycling helps mitigate environmental impact.

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14
Q

What are the disadvantages of recycling polymers?

A

Plastics need to be collected, transported, and sorted, which uses energy and manpower, making it expensive.

These processes can offset some environmental benefits.

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15
Q

What is a consequence of burning polyalkenes?

A

Produces energy but may release poisonous carbon monoxide if combustion is incomplete.

This adds to carbon dioxide levels in the atmosphere.

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