polymers
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What are addition polymers?
when an unsaturated monomers react to form a polymer monomers contain C=C bonds chains form when same basic unit is repeated over and over
why are poly (alkenes) chemically inert?
due to strong C-C and C-H bonds and non-polar nature of the bonds and therefore are non-biodegradable
what happens in condensation polymerisation?
there are two different monomers that add together, and a small molecule is usually given off as a side-product eg H2O or HCl the monomers usually have the same functional group on both ends of the molecule eg di-amine di-carboxylic acid
what are the reactions for forming polyesters via condensation polymerisation?
carboxylic acid + alcohol –> ester + water acyl chloride + alcohol –> ester + HCl
what are the equations for forming polyamides via condensation polymerisation?
carboxylic acid + amine –> amide + water acyl chloride + amine –> amide + HCl
what is bad about using dicarboxylic acids to make polyesters or amides, why is using acyl chlorides better?
using the carboxylic acid would need an acid catalyst and would only give an equilibrium mixture the more reactive acyl chloride goes to completion and does not need a catalyst, but does produce hazardous fumes of HCl
what is the other way of making polyesters?
hydroxycarboxylic acid monomer, just need 2 to react together
what is terylene?
a common polyester used in clothing, tire cords formed from benzene-1,4-dicarboxylic acid and ethane-1,2-diol
what is nylon 6,6?
a common polyamide 6,6 stands for 6 carbons in each of the monomers used in textile fibres it is formed via reaction between hexanedioic acid and hexane-1,6-diamine
what is kevlar?
polyamide used in bulletproof vests
what kind of intermolecular forces exist in polyesters?
permanent dipole- permanent dipole forces between the C=O groups in the different chains also VDW between chains
what kind of intermolecular forces exist in polyamides?
hydrogen bonding between the oxygen in C=O and the H in N-H groups in different chains also VDW forces polyamides will therefore have higher melting points than polyesters
how can reactivity of condensation polymers be explained?
presence of polar bonds which can attract attacking species such as nucleophiles and acids
how can polyesters and polyamides be broken down?
by hydrolysis by acid or alkali this hydrolysis will result in original monomers forming- although the carboxylic acid or amine group will be in salt form depending on whether the conditions are acidic or alkaline this means they are BIODEGRADEABLE
describe landfill as a method of disposal of polymers?
-most common method of disposal of waste in UK -many are now reaching capacity -european regulations will mean councils charged much more for using landfill -most polymers (polyalkenes) are non-biodegradable and take many years to break down -could use more biodegradable plastics eg polyamides ad cellulose and starch based polymers to improve rates of decomposition
describe incineration as a method of disposal of polymers?
rubbish is burnt and energy produced is used to generate electricity some toxins can be released on incineration modern incinerators can burn more efficiently and most toxins and pollutants can be removed greenhouse gases will still be emitted though volume of rubbish greatly reduced
describe recycling as a method of disposal of polymers?
saves raw materials- nearly all polymers are formed from compounds sourced/ produced from crude oil, saves precious resources polymers need collecting/ sorting- expensive process in terms of energy and manpower polymers can only be recycled into the same type- so careful separation needs to be done thermoplastic polymers can be melted down and reshaped