Polymers Flashcards

(55 cards)

1
Q

Condensation reactions are formed by reactions between:

A

• dicarboxylic acids and diols (polyesters)
• dicarboxylic acids and diamines (polyamides)
• amino acids (polypeptides)

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2
Q

3 main types of condensation polymers

A

• polypeptides
• polyamides
• polyesters

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3
Q

Condensation polymerisation is where

A

2 different monomers with at least 2 functional groups react together
-> when they react a link is made and water is eliminated (hence condensation)

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4
Q

What does the link formed determine

A

The type of polymer produced

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5
Q
A
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6
Q

What links are formed in polyamides

A

Amide links

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7
Q

Why does we have to use dicarboxylic acids and diamines or diols

A

Because they have to have functional groups either side which allows for chains to be formed

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8
Q

What is kevlar

A

A polyamides used in bulletproof vests, car tyres and some sports equipment

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9
Q

What is kevlar made from

A

Benzene-1,4-dicarboxylic acid AND 1,4-diaminobenzene

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10
Q

What is nylon 6,6

A

A polyamide that is used in ropes, carpets, clothing and parachute fabric

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11
Q

What is Nylon 6,6 made from

A

Hexanedioic acid AND 1,6-diaminohexane

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12
Q

What links are formed in polyesters

A

Ester links

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13
Q

What is a diol

A

A molecule with 2 alcohol groups

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14
Q

What is terylene

A

A polyesters used in plastic drinks bottles and clothes

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15
Q

What is terylene made from

A

Benzene-1,4-dicarboxylic acid AND ethane-1,2-diol

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16
Q

Condensation can be..

A

Hydrolysed to produce the original monomers

-> it’s jsut the reverse of polymerisation

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17
Q

What kind of bonds do condensation polymers have

A

Polar bonds

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18
Q

Why do condensation polymers have polar bonds

A

Becuase of the C-O and C-N bonds that exist in polymers

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19
Q

Condensation polymers are usually more..

A

Rigid and stronger than addition polymers

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20
Q

What bonds exist between condensation polymers chains

A

Hydrogen bonds
Dipole-dipole bonds
VDWs forces

-> making them stronger than addition polymers

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21
Q

Why can condensation polymers break down more readily in water

A

They have hydrogen bonds and so can dissolve

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22
Q

What are synthetic polymers made from and used to make

A

Monomer units

Plastic bottles, digital technology and non stick coatings on pans

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23
Q

Condensation polymers are..

A

Biodegradable

24
Q

Why are condensation polymers biodegradable

A

They are polar and so susceptible to attack from nucleophiles

-> they are broken down by hydrolysis slowly

25
What are polyalkenes
Addition polymers -> they are saturated molecules
26
Properties of polyalkenes
• saturated molecules • non-polar so unreactive • good in foods as they don’t react • don’t degrade well in landfill
27
What does polyalkenes not being polar mean
They are unreactive
28
Landfill is useful for disposing plastics that:
• are too difficult to recycle • are too difficult to separate from other materials • there’s not enough plastic to extract to make it economically viable
29
When waste decomposes in landfill..
It produces methane which is a greenhouse gas • there’s also a risk of water contamination from leaching
30
What’s wrong with landfill
- not sustainable as large amounts of land is needed - expensive to use land - there’s a need to reduce our reliance on landfill
31
What is incineration
Burning waste plastics -> used if the plastics can’t be recycled
32
Why is incineration good
It can be used to generate electricity
33
Why is incineration bad
Burning plastics can release toxic fumes -> especially chlorine based products like PVC which produce harmful HCl gases when burned
34
What is used to balance the release of harmful gas in incineration
Flue gas scrubbers
35
What do flue gas scrubbers do
Neutralise acidic gases produced like HCl
36
How do flue gas scrubbers work
-> they work by firing a base at the flue gases
37
Ways of disposing plastics
• landfill • incineration • recycling
38
Most polymers are made from..
Crude oil which is non renewable
39
Recycling means reducing..
Dependency on crude oil for making plastics
40
Some plastics can be..
Remoulded into new objects Like polypropene
41
Ways plastics can be recycled
• remoulded into new objects • cracked into monomers to be used as an organic feedstock for plastics or other substances
42
Advantages of recycling plastics
- Cheaper than making them from scratch - Less carbon dioxide is produced recycling plastics than incinerating - Recycling reduces the reliance on landfill - Recycling preserves non-renewable raw materials such as crude oil
43
Disadvantages of recycling plastics
- Plastics can be contaminated with other materials - It’s difficult to recycle plastics due to the wide variety of different plastics - It’s difficult to re-make the original plastic from recycled material - Sorting and processing plastics to be recycled is expensive compared with incineration
44
What kind of links to polypeptides have
Amide links (peptide)
45
Why are addition polymers nonpolar
They only consist of C-C and C-H bonds -> rely on weaker induced dipole-dipole forces between chains
46
The presence of stronger intermolecular forces makes condensation polymers:
• More rigid and less flexible • Stronger, with higher melting and boiling points compared to addition polymers
47
Monomers used in addition polymerisation
Alkenes
48
Monomers used in condensation polymerisation
Carboxylic acids, acyl chlorides, amines, alcohols, amino acids
49
Polymer chain in addition polymerisation
Continuous chain of carbon atoms
50
Polymer chain in condensation polymerisation
Constrains ester or amide bonds
51
Products formed in addition polymerisation
Polymer only
52
Products formed in condensation polymerisation
Polymer and small molecule (like water)
53
2 main approaches to recycling waste plastics
Mechanical recycling Feedstock recycling
54
Mechanical recycling
Involves sorting, cleaning and remoulding waste plastics into new objects without significant altering the chemical structure of the polymer
55
Feedstock recycling
Breaks down polymers into their constituent monomers through cracking -> these monomers can then be used as raw materials for the synthesis of new plastics and other organic chemicals