1Condensation polymerisation
Where 2 different monomers with at least 2 functional groups react.
Form link and water removed
2How polyamides formed
Via reacting dicarboxylic acids and diamines. Forms AMIDE LINK
OH removed from acid and H removed from amine

3Kevlar?
Polyamide for bulletproof vest,car tyres
Made from benzene-1,4-dicarboxylic acid and 1,4-diaminobenzene

4Nylon 6,6
Polyamide for ropes,clothing, carpet
Made from hexanedioc acid and 1,6 diaminohexane
5Polyesters?
React dicarboxylic acids and diols and forms ester links and releases H20

6Terylene?
Polyester for bottles,clothes,sheeting
Made from benzene-1,4-dicarboxylic acid and ethane-1,2-diol

7Hydrolysis of condensation polymers?
Can be hydrolysed via water to produce original monomers.
Straight up reverse
8Polarity in condensation polymers?
Have polar bonds by C-O and C-N which can interact with other chains and form strong INFS.
So they are susceptible from nucleophile attacks.
Biodegradable and broken down by hydrolysis slowly unlike addion polymers

9Ways to dispose plastic
Landfill
Incineration
Recycle
10Disposal of plastic?(1st way)
Landfill useful for disposing plastics which are too difficult to recycle/not worth doing
The decomposition leads to greenshouse gases and risk of water contamination via leaching
Not sustainable and expensive
11Disposal of plastic (2nd way)
Incineration can be used for unrecyclable plastic.
Energy from burning can be used to generate electricity
Produces toxic fumes and flue gas scruppers used to netrulastix acidic gas(hcl)
12Disposal of plastic (3rd way)
Recycling leads to less dependency on crude oil
Some plastic can be recycled and remoulded
13Pros and cons of recycle.